SYNTHESIS POLYETHERSULFONE-BASED AMPHIPHILIC BLOCK COPOLYMERS & DEVELOPMENT OF SINGLE-ION CONDUCTORS FOR
LITHIUM ION BATTERIES
By
Hui Zhao
A DISSERTATION
Submitted to Michigan State University
in partial fulfillment of the requirements for the degree of
DOCTOR OF PHILOSOPHY
Chemistry
2012
ABSTRACT
SYNTHESIS POLYETHERSULFONE-BASED AMPHIPHILIC BLOCK COPOLYMERS & DEVELOPMENT OF SINGLE-ION CONDUCTORS FOR
LITHIUM ION BATTERIES
By
Hui Zhao
Polyethersulfone (PES) membranes often foul easily because of their
hydrophobicity, and addition of amphiphilic PES block copolymers to
membrane formulations may help overcome this problem. This dissertation
explores the synthesis and aggregation properties of relevant amphiphilic ABA
block copolymers, where PES is the hydrophobic B block and poly(2-
hydroxyethyl methacrylate) or poly(2-hydroxypropyl methacrylate) are the
hydrophilic A blocks. 1H nuclear magnetic resonance (NMR) spectroscopy,
Fourier transform infrared spectroscopy (FT-IR) and thermogravimetric
analysis (TGA) confirm the block copolymer synthesis, and 1H NMR spectra
and TGA also provide consistent data on copolymer compositions.
Aggregation behavior of the copolymers in solvent/non-solvent mixture is
studied using NMR and dynamic light scattering (DLS).
Lithium ion batteries are now ubiquitous, but concentration polarization is
still a problem in the currently used battery electrolytes, especially in
high-current applications. Immobilizing anions and having lithium cations
contribute to most of the ionic conductivity is a good solution to address this
problem. This work aims to create nanoparticle-containing electrolytes using
silica nanoparticles modified with polyanions that have Li+ as the counterion.
Anion mobility is restricted by the polyanion polymer backbones, which is
further immobilized by the nanoparticles. The polyelectrolyte-grafted
nanoparticles were synthesized by surface atom transfer radical
polymerization (ATRP) of monomers from initiator-grafted silica nanoparticles.
To prepare a lithium-ion conductor, the polyelectrolyte-grafted nanoparticles
were blended with polyethyleneglycol (PEG) oligomer. Because the anions are
immobile, lithium is the only ion that conducts current. AC impedance shows
that the best conductivity is from a Bis(trifluoromethanesulfonyl)imide (TFSI)
analogue monomer around 10-6
S/cm, which is in the same range as a
monolayer-grafted silica nanoparticle system using similar TFSI analogue
structure. A proposed model shows that the multilayer-grafted nanoparticles
only have outermost layer of lithium cations accessible to the solution,
because of the low solubility of polyelectrolytes in the PEG solvent.
Direct modification of PEG via alkyne-azide or thiol-ene click chemistry as
single lithium ion conductor. To make sure 1,2,3-triazole or sulfur structure
from click chemistry is not impeding lithium transport, we synthesize
1,2,3-triazole and sulfur containing PEGs via step growth polymerization.
Conductivity measurement of lithium perchlorate with triazole containing PEG
or sulfur containing PEG shows similar data as the pure PEG, which proves
that click chemistry could be applied in the development of single-ion
conductors for Lithium Ion Batteries.
Copyright by HUI ZHAO
2012
v
ACKNOWLEDGEMENTS
Dr. Gregory Baker – for his patience, encouragement, advice and intellectual
generosity
Dr. Merlin Bruening – for much appreciated advice and discussions on my
research project
Dr. William Wulff, Dr. Milton Smith and Dr. Babak Borhan– for being my
committee member
Many people, past and present, in the lab, Qin Yuan, Sampa Saha, Tomas
Jurek, Georgina Comiskey, Wen Yuan, Quanxuan Zhang, Heyi Hu, Yiding Ma,
Zhe Jia, Greg Spahlinger, Salinda Wijeratne.
Many people, in the department, in particular, Daniel Holms, Kathryn Severin
for their help on the instruments.
Finally, I would like to thank my family for their love and support.
vi
TABLE OF CONTENTS
LIST OF TABLES ............................................................................................ viii
LIST OF FIGURES ............................................................................................ x
LIST OF SCHEMES ....................................................................................... xiv
Chapter 1 Introduction ....................................................................................... 1 Part I: Synthesis of Polyethersulfone (PES)-Based Amphiphilic Block Copolymers ..................................................................................................... 1 Part II: Synthesis of Comb-Polyethyleneoxide (PEO) via Click Chemistry- New polymers for Possible Lithium Ion Conductors ....................................... 3 References ..................................................................................................... 8
Chapter 2 Synthesis of Polyethersulfone (PES)-Based Amphiphilic Block Copolymers ...................................................................................................... 13
Introduction ................................................................................................... 10 Polysulfone Materials and Their Application as Water Treatment Membranes ............................................................................................... 10 Block Copolymers ..................................................................................... 13 Polysulfone-Based Amphiphilic Copolymers ............................................ 17 Self-assembly of Block Copolymers ......................................................... 22 Block Copolymers as Phase Inversion Membrane Materials ................... 24 Unique Aspects of Self-assembly of Polysulfone-Based Block Copolymers .................................................................................................................. 27
Results and Discussion ................................................................................ 29 Purification of Hydroxypropyl Methacrylate (HPMA) Isomers .................. 30 Synthesis of PES with Hydroxyl End Groups ........................................... 33 Synthesis of a PES Macroinitiator and Use of a Model Compound to Explore the ATRP Catalytic System ......................................................... 36 Polymerization from a PES Macroinitiator ................................................ 42 GPC Analysis of HEMAn-PESm-HEMAn and HPMAn-PESm-HPMAn Block Copolymers ..................................................................................... 47 Infrared Spectra of the Block Copolymers ............................................... 53 TGA of the Block Copolymers .................................................................. 57 Critical Water Content (CWC) Values of PES and PES-based Block Copolymers ............................................................................................... 63 Aggregation of Block Copolymers in Dilute Solutions-NMR and DLS Studies ...................................................................................................... 72
vii
Conclusion .................................................................................................... 81 Experimental Section ................................................................................... 82 Appendix A ................................................................................................... 91 References ................................................................................................... 98
Chapter 3 Use of the Nanoparticles and Click Chemistry in the Development of Single-ion Conductors for Lithium Ion Batteries ............................................ 102
Introduction-Ion Conduction in Lithium Ion Batteries ................................. 102 Results and Discussion .............................................................................. 106
Single-ion Conductors Containing Nanoparticles with Immobilized Anions ................................................................................................................ 106 Single-ion Conductors Prepared Using Nanoparticles Modified by Grafting of Polyanions .......................................................................................... 109 Towards Click Chemistry for Synthesizing Single-ion Conductors with a High Density of Lithium Ion PEO ............................................................ 113
Conclusions ................................................................................................ 126 Experimental Section ................................................................................. 127 Appendix B ................................................................................................. 135 References ................................................................................................. 154
viii
LIST OF TABLES
Table 2.1. Different conditions for synthesis of PES and the molecular weights and PDI values of the resulting polymer. ......................................................... 33
Table 2.2. Block Copolymers with their Molecular Weights and PDI Values. ......
......................................................................................................................... 46
Table 2.3. PDIs of various copolymers as determined from GPC data or calculated using equation (2) ........................................................................................... 52
Table 2.4. PolyHEMA Content in Copolymer Samples as Calculated from NMR Spectra and TGA under nitrogen ..................................................................... 60
Table 2.5. PolyHPMA Content in Copolymer Samples as calculated from NMR spectra and TGA. ............................................................................................. 63
Table 2.6. Commercial Polyethersulfones and their Molecular Weights, PDI Values and Terminal Groups. ........................................................................... 64
Table 2.7. Solubility Parameters of Several Solvents and Polymers at 25 oC. ......................................................................................................................... 68
Table 2.8. Evolution of the proton NMR signals from HEMA22-PES34-HEMA22 with increasing of D2O content in the DMSO-d6 solvent. ............................................................................................................. 75
Table 2.9. DLS particle sizes and particle volume percentages for aggregates of HEMA22-PES34-HEMA22 formed in NMP/water mixtures. The mixtures contained 1 mg/mL HEMA22-PES34-HEMA22. .............................................. 77
Table 2.10. DLS particle sizes and particle volume percentages for aggregates of HEMA22-PES34-HEMA22 formed in NMP/water mixtures. The mixtures contained 10 mg/mL HEMA22-PES34-HEMA22 ............................................ 79
ix
Table 2.11. DLS particle sizes and particle volume percentages for aggregates of HEMA22-PES34-HEMA22 formed in NMP/water mixtures. The mixtures contained 30 mg/mL HEMA22-PES34-HEMA22. ............................................ 80
Table 2.12. Polystyrene standards used to calibrate the results of GPC in DMF. ......................................................................................................................... 84
Table 3.1. Lithium transference numbers for several lithium salts in battery solvents. ......................................................................................................... 105
Table 3.2. Particle weight percentages and O/Li for electrolytes prepared from Si-C5NTfLi dispersed in PEGDME-500. ........................................................ 108
Table 3.3. Particle weight percentages and O/Li ratios for electrolytes prepared from Si-TfMALi dispersed in PEGDME-500. ................................................. 110
x
LIST OF FIGURES
Figure 2.1. Equilibrium morphologies in AB diblock copolymers.. ................... 24
Figure 2.2. Phase inversion membranes made from PSf (upper left: SEM top view, upper right: edge view, NMP solvent), and PES (bottom: SEM edge view DMAc solvent). ................................................................................................. 26
Figure 2.3. SEM images of membranes prepared by phase inversion of poly(styrene)-co-poly(4-vinylpyridine). Peinemann’s work. Edge view (left), top view (right). Scale bars correspond to 500 nm.. .............................................. 27
Figure 2.4. Proton NMR 500 MHz spectra of an HPMA isomer mixture (bottom) and purified 2-hydroxypropyl methacrylate (top) in deuterated chloroform.. ... 32
Figure 2.5. ProtonNMR 500 HMz spectra of bisphenol sulfone (bottom) and BisphenolS-I (top) in deuterated DMSO... ..................................................... 37
Figure 2.6. ATRP kinetic plot for polymerization of HEMA using BisphenolS-I as an initiator and CuBr/PMDETA as the catalyst in DMF, the initial monomer concentration was 2 M... .................................................................................. 38
Figure 2.7. ATRP kinetic plot for polymerization of HEMA using ethyl bromoisobutyrate as an initiator and CuCl/CuCl2/PMDETA as the catalyst in NMP, the initial monomer concentration was 2 M... ........................................ 40
Figure 2.8. ATRP kinetic plot for polymerization of HEMA using ethyl BisphenolS-I as the initiator and CuCl/CuCl2/PMDETA as the catalyst in NMP, the initial monomer concentration was 2 M... .................................................. 41
Figure 2.9. ATRP kinetic plot for polymerization of HEMA using a PES macroinitiator and CuCl/CuCl2/PMDETA as the catalyst in NMP, the initial monomer concentration was 1.3 M... .............................................................. 42
Figure 2.10. Proton NMR 500 MHz spectra of (a) NMP, (b) HEMA26-PES42- HEMA26 and (c) macroinitiator in DMSO-d6... ............................................... 44
Figure 2.11. Gel-permeation chromatograms of (a) PES51 and (b) the copolymer HEMA9-PES51-HEMA9... .............................................................. 47
xi
Figure 2.12. Gel-permeation chromatograms of (a) PES42 (b) copolymer HEMA13-PES42-HEMA13 and (c) HEMA26-PES42-HEMA26... ................... 49
Figure 2.13. Gel-permeation chromatograms of (a) PES34 and (b) HEMA22- PES34-HEMA22... ........................................................................................... 50
Figure 2.14. An ABA block copolymer with monodisperse A block and polydisperse (PDI=2.0) B blocks... .................................................................. 51
Figure 2.15. Gel-permeation chromatograms of (a) PES42, (b) HPMA12- PES42-HPMA12 and (c) HPMA26-PES42-HPMA26... ................................... 53
Figure 2.16. IR spectra of (a) PES, (b) polyHEMA and (c) HEMA22-PES34- HEMA22... ........................................................................................................ 54
Figure 2.17. IR spectra of (a) HEMA9-PES51-HEMA9, (b) HEMA13-PES42- HEMA13, (c) HEMA26-PES42-HEMA26 and (d) HEMA22- PES34-HEMA22....
......................................................................................................................... 55
Figure 2.18. IR Spectra of (a) PES, (b) polyHPMA and (c) HPMA12-PES42- HPMA12... ........................................................................................................ 56
Figure 2.19. IR spectra of (a)HPMA12-PES42-HPMA12 and (b) HPMA26- PES42-HPMA26... ........................................................................................... 57
Figure 2.20. TGA data for PES and several polyHEMA-co-PES-co-polyHEMA samples heated under air (samples were held at 120 oC until the weight was constant (~ 3 hours) before heating at 10 oC/min) (a) PES, (b) HEMA9-PES51- HEMA9, (c) HEMA13-PES42-HEMA13, (d) HEMA26-PES42-HEMA26 and (e) HEMA22-PES34-HEMA22... ........................................................................... 58
Figure 2.21. TGA data for PES, polyHEMA and polyHEMA-co-PES-co- polyHEMA samples heated under nitrogen (samples were held at 120 oC until weight was constant (~ 3 hours) before heating at 10 oC/min). (a) PES, (b) polyHEMA, (c) HEMA9-PES42-HEMA9, (d) HEMA13-PES42-HEMA13, (e) HEMA26-PES42-HEMA26 and (f) HEMA22-PES34-HEMA22... .................... 59
xii
Figure 2.22. TGA data for PES and polyHPMA-co-PES-co-polyHPMA samples heated under air (samples were held at 120 oC until the weight was constant (~ 3 hours) before heating at 10 oC/min) (a) PES, (b) HPMA12-PES42- HPMA12 and (c) HPMA26-PES42-HPMA26... ............................................... 61
Figure 2.23. TGA data for PES and polyHPMA-co-PES-co-polyHPMA samples heated under nitrogen (samples were held at 120 oC until weight was constant (~ 3 hours) before heating at 10 oC/min) (a) PES, (b) polyHPMA, (c) HPMA12- PES42-HPMA12 and (d) HPMA26-PES42-HPMA26... ................................... 62
Figure 2.24. Room-temperature critical water content (CWC) values of different PES materials in four solvents (NMP, DMF, DMSO, DMAc) (a) Ultrason 2020 P from BASF, (b) Ultrason 6020 P from BASF, (c) Veradel 3600 RP from Solvay, (d) Veradel 3000 RP from Solvay and (e) PES synthesized at MSU Mn=10,000, PDI=2.0. (Each data point is an average from three independent samples, and the data points often obscure the error bars.).. .......... .................................................................................................................................................... 65
Figure 2.25. Room-temperature CWC values for several PES samples in NMP. (1) Ultrason 6020P, (2) Veradel 3000RP, (3) Ultrason 2020P, (4) Veradel 3600RP and (5) home-made PES. (Each data point is an average from three independent samples, and the data points often obscure the error bars.).. ......... .................................................................................................................................................... 70
Figure 2.26. Room-temperature CWC values in NMP for (a) PES, (b) HPMA26 -PES42-HPMA26 and (c) HEMA22-PES34-HEMA22. (Each data point is an average from three independent samples, and the data points often obscure the error bars.).. ............................................................................................... 71
Figure 2.27. Proton NMR 500 MHz Spectra of HEMA22-PES34-HEMA22 in DMSO-d6/D2O co-solvents with varying amounts of water... ......................... 73
Figure 2.28. DLS size distributions for HEMA22-PES34-HEMA22 (1 mg/mL at 25 oC) dissolved in NMP and NMP/water co-solvents with different volume ratios... ............................................................................................................. 76
Figure 2.29. DLS size distributions for HEMA22-PES34-HEMA22 (10 mg/mL at 25 oC) dissolved in NMP and NMP/water co-solvents with different volume ratios... ............................................................................................................. 78
xiii
Figure 2.30. DLS size distributions for HEMA22-PES34-HEMA22 (30 mg/mL at 25 oC) dissolved in NMP and NMP/water co-solvents with different volume ratios... ............................................................................................................. 80
Figure 3.1. Schematic diagram of a lithium ion battery containing a metal oxide cathode and a graphite anode. The figure also shows redox reaction during discharge... .................................................................................................... 103
Figure 3.2. Concentration polarization during discharge of a lithium ion battery... ......................................................................................................... 104
Figure 3.3. Temperature-dependent conductivity of electrolytes containing different fractions of Si-C5NTfLi dispersed in PEGDE-500. These results were obtained by Fadi Asfour, and I repeated some of the measurements... ....................................................................................................................... 108
Figure 3.4. Temperature-dependent conductivity of electrolytes containing different fractions of Si-TfMALi dispersed in PEGDE-500. The various fractions of particles (see Table 3.3) lead to the different O/Li ratios shown in the figure... ....................................................................................................................... 110
Figure 3.5. Temperature-dependent conductivity for (a) Si-C5NTfLi at O/Li 425 and (b) Si-TfMALi at O/Li 32, both samples contain ~19 wt% modified particles... ....................................................................................................... 111
Figure 3.6. Kinetics of step-growth polymerization between dipropargyl and diazido tetraethylene glycol... ........................................................................ 122
Figure 3.7. Conductivities of mixtures of LiClO4 with pure PEO (black squares) and triazole-containing PEO (red circles) at different ratios of PEO to LiClO4. The O/Li ratios in the mixture were determined from the masses of LiClO4 and PEO added, and these ratios only include the O atoms from PEO. Measurements occurred at 90 oC... ............................................................... 124
Figure 3.8. Conductivities of mixtures of LiClO4 with pure PEO (black squares) and thioether-PEO (red circles) at different ratios of PEO to LiClO4. The O/Li ratios in the mixture were determined from the masses of LiClO4 and PEO added, and these ratios only include the O atoms from PEO. Measurements occurred at 90 oC... ........................................................................................ 125
xiv
LIST OF SCHEMES
Scheme 1.1. Structure of the ABA amphiphilic block copolymers synthesized in this study... ..................................................................................................... 2
Scheme 1.2. Small molecule model (BisphenolS-I) initiator used to explore ATRP catalytic systems for synthesis of block copolymers. This molecule mimics the structure of PES macroinitiators... ................................................... 2
Scheme 1.3. Grafting of polyelectrolytes to nanoparticles to create single-ion conductors... ...................................................................................................... 4
Scheme 1.4. Monolayer-modified silica nanoparticles for single ion conductors... ...................................................................................................... 6
Scheme 2.1. Chemical Structures of Bisphenol A Polysulfone (PSf) and Polyethersulfone (PES)... ................................................................................ 12
Scheme 2.2. Reactions invovled in ATRP... ..................................................... 14
Scheme 2.3. Possible architectures of copolymers synthesized from two monomers, A and B... ...................................................................................... 16
Scheme 2.4. Structure of the block copolymer synthesized by Jo... ............... 18
Scheme 2.5. PSf-based amphiphilic block copolymer prepared by Moore et al. for formation of membranes... .......................................................................... 19
Scheme 2.6. PSf-based amphiphilic block copolymers synthesized by Wang el al for use as membrane additives... ................................................................. 20
Scheme 2.7. PSf-based graft copolymer prepared by Yi... ............................. 21
Scheme 2.8. PES-based graft copolymer synthesized by Yi et al... ............... 21
Scheme 2.9. Protocol for making phase-inversion membranes... ................... 25
xv
Scheme 2.10. Selective reaction of triphenylmethyl chloride with the primary alcohol in hydroxypropyl methacrylate mixtures and subsequent isolationof 2-hydroxypropyl methacrylate.......................................................................... 30
Scheme 2.11. Synthesis of hydroxyl terminated polyethersulfone (PES)... .... 34
Scheme 2.12. Mechanism of etherification in synthesis of PES... .................. 35
Scheme 2.13. Synthesis of a macroinitiator from OH-terminated PES... ........ 36
Scheme 2.14. Synthesis of BisphenolS-I... .................................................... 37
Scheme 2.15. Characteristic protons for calculation of copolymer composition from NMR spectra... ......................................................................................... 85
Scheme 2.16. Characteristic protons for calculation of copolymer composition from NMR spectra... ......................................................................................... 86
Scheme 3.1. Monolayer modified silica nanoparticle Si-C5NTfLi (silica nanoparticle derivatized with lithiated N-pentenyl triflouromethane sulfonimide)... ................................................................................................. 106
Scheme 3.2. Method for determining the Li+ content of PEO-based electrolytes... .................................................................................................. 107
Scheme 3.3. Silica nanoparticles prepared by grafting lithiated poly (trifluoromethane sulfonic aminoethyl-methacrylate) (Si-TfMALi) from the surface... ........................................................................................................ 109
Scheme 3.4. Proposed qualitative conformations of monolayer Si-C5NTfLi (top) and multilayer Si-TfMALi (bottom) at 30 oC and at 80 oC... ........................... 112
Scheme 3.5. Proposed single-ion conductors prepared by synthesis of PEO containing alkene or alkyne groups and subsequent attachment of anions to these groups via click chemistry... ................................................................. 114
Scheme 3.6. Polysulfone structures synthesized by Bielawski’s et al for proton-conduction... ....................................................................................... 115
xvi
Scheme 3.7. Polyacrylate structures prepared by Martwiset et al. for formation of membranes that exhibit proton conductivity at 200 oC... ........................... 116
Scheme 3.8. Poly(ether ether ketone) prepared by Gao et al for reaction with 3-mercaptopropyltrimethoxysilane via click chemistry... ............................... 117
Scheme 3.9. The thioether and triazole structures that result from (a) thiol-ene and (b) alkyne-azido click chemistry, respectively... ..................................... 117
Scheme 3.10. (a) Scheme of ideal lithium transport in an electrolyte material and (b) scheme of lithium transport if the click functionality (triazole or thioether) impedes Li+ transport... .................................................................................. 118
Scheme 3.11. (a) Monomers synthesized to prepare triazole-containing PEO, (b) monomers to that will react to give sulfur-containing PEO... ................... 119
Scheme 3.12. Two methods for synthesis of dipropargyl tetraethylene glycol... ....................................................................................................................... 120
Scheme 3.13. Synthesis of several step-growth polymerization monomers via the ditosyl derivative... .................................................................................. 121
Scheme 3.14. Synthesis of diallyl tetraethylene glycol.. ............................... 121
Scheme 3.15. Step-growth polymerization of diazido and dipropargyl tetraethylene glycol... ..................................................................................... 122
Scheme 3.16. Step-growth polymerization of dithiol and diallyl tetraethylene glycol... ........................................................................................................... 123
1
Chapter 1. Introduction
There are two parts to this dissertation: chapter 2 describes the synthesis of
polyethersulfone (PES)-based block copolymers that are relevant to
membrane modification, and chapter 3 explores potential single-ion
conductors based on comb-polyethyleneoxide (PEO) materials. Such
conductors are important elements of lithium ion batteries. Below I briefly
summarize the two projects, and each chapter contains a more extensive
introduction.
Part I: Synthesis of Polyethersulfone (PES)-Based Amphiphilic Block
Copolymers
Polyethersulfone (PES) is widely employed in water-treatment membranes
because of its chemical and thermal stability. However, the hydrophobic nature
of PES may cause severe fouling problems.2 The introduction of ABA block
copolymers (Scheme 1.1) into PES membranes sometimes greatly improves
their filtration properties.3 A PES B block facilitates incorporation into the
membrane, and hydrophilic A blocks can create more wettable surfaces that
resist fouling.
2
O Om
nhydrophobic block
SO O
O
OH
hydrophilic block
polyethersulfone (PEO)
O Om
OH
poly(hydroxylethyl methacrylate)polyHEMA
poly(2-hydroxylpropyl methacrylate)polyHPMA
Scheme 1.1. Structure of the ABA amphiphilic block copolymers synthesized
in this study. (For interpretation of the references to color in this and all other
figures, the reader is referred to the electronic version of this dissertation.)
Scheme 1.2. Small molecule model (BisphenolS-I) initiator used to explore
ATRP catalytic systems for synthesis of block copolymers. This molecule
mimics the structure of PES macroinitiators.
Our synthesis of ABA copolymers relies on ATRP from PES macroinitiators.
To explore atom transfer radical polymerization (ATRP) catalyst systems for
polymerization, BisphenolS-I served as a model compound for the PES
macroinitiator (Scheme 1.2). NMR characterization is much simpler with this
3
small molecule than a polymer. We tested different combinations of metal
catalyst and ligand, and CuCl/CuCl2/N,N,N′,N′,N′′-pentamethyldiethylene
triamine (PMDETA) proved effective for controlled polymerization of
2-hydroxyethyl methacrylate (HEMA) and 2-hydroxypropyl methacrylate
(HPMA). This catalyst system enabled synthesis of polyHEMA-PES-
polyHEMA and polyHPMA-PES-polyHPMA on a 10-20 g scale. Fourier
transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA)
and 1H NMR show successful synthesis of these block copolymers. Dynamic
light scattering studies reveal copolymer aggregates (radii of 60 nm) in 20 vol%
water in N-methylpyrrolidone. These copolymers may prove valuable in
membrane modification, and we have delivered them to Pall Corporation for
their investigation.
Part II: Synthesis of Comb-Polyethyleneoxide (PEO) via Click Chemistry-
New Polymers for Possible Lithium Ion Conductors
When a lithium ion battery discharges, electrons flow from the anode to the
cathode through the external circuit. Simultaneously, inside the cell lithium
cations formed at the anode migrate and intercalate into the cathode. Ideally,
lithium ions carry all the current within the cell. Typical values of the Li+
transference number (tLi+, the fraction of the current carried by Li+) in
electrolytes range from 0.2-0.3, however, which indicates the anion is the
dominant species in carrying current. Since a low tLi+ limits a battery’s power
density and often affects the chemical stability of electrolytes, development of
4
electrolytes with near-unity lithium-ion transference numbers is important.
Scheme 1.3. Grafting of polyelectrolytes to nanoparticles to create single-ion
conductors.1
In research for my MS thesis, I investigated several nanoparticle systems
where Li+ is a counterion to anionic groups immobilized on grafted polymers
(Scheme 1.3). Nanoparticle-containing electrolytes were prepared by mixing
the purified particles and low-molecular weight (~500 g/mol) polyethylene
glycol dimethyl ether (PEGDME-500). Movement of the anions was largely
restricted because of the surface-anchored polymer backbones, so Li+
became the only ion conducting current.
The MS thesis explored four different polymer structures (Scheme 1.3) with
the aim of improving the ionic conductivity of the nanoparticles/PEGDME-500
blend. The first grafted polymer, poly(lithium styrene sulfonate) was initially
synthesized from sodium styrene sulfonate monomer, and lithium exchange
5
gave poly(lithium sulfonate styrene). In a second case, polyethylene glycol
methyl ether methacrylate (PEGMA) was copolymerized with the styrene
sulfonate, to facilitate transport of lithium cations and increase the miscibility of
the particles with PEGDME-500. The third structure used phosphonates, which
have two lithium counterions per monomer, to increase the lithium content.
The room temperature conductivity of these electrolytes was 10-7
S/cm. This is
several orders of magnitude lower than the conductivity of electrolytes
employed in current lithium ion batteries, and one or two orders of magnitude
lower that current single-ion conductors.
To further improve the conductivity, the fourth structure was inspired by
lithium bis(trifluoromethane sulfonyl) imide (LiTFSI). High conductivity
correlates with the dissociation of Li+ from the anion, and therefore anions such
as ClO4-, PF6
- and bis(trifluoromethylsufonyl amide) (TFSI) are commonly used
in electrolytes. We synthesized a polymerizable analogue of TFSI and grew the
corresponding polymers from silica nanoparticles. The maximum conductivity,
10-6
S/cm, occurred at an oxygen to lithium ratio of 32. The O in this ratio
comes exclusively from ether oxygens in PEGDME-500, and Li comes from the
amount of the lithium cations in the electrolytes. The value of O/Li is a common
measure of the lithium concentration in the electrolytes.
6
Scheme 1.4. Monolayer-modified silica nanoparticles for single ion
conductors.4
We expected much higher conductivity than 10-6
S/cm, because the
polyelectrolyte constitutes 70~90 wt% of the polymer grafted particles. This
high polyelectrolyte content should supply a large amount of free lithium cations
to contribute to a high conductivity. A previous group member, Fadi Asfour,
investigated monolayer-coated silica nanoparticles as single-ion conductors
(Scheme 1.4), and these materials mixed with PEGDME-500 also have a
conductivity of 10-6
S/cm.4 A possible explanations for the low conductivity with
a dense layer of polyelectrolyte on the particle surface is that not all of the
lithium cations have access to the solvent (PEGDME-500). Most of the
polyelectrolytes are buried near the silica surface and do not contribute to
conductivity.
We then planned to directly modify the PEO structure to obtain a single ion
conductor via alkyne-azido or thiol-ene click chemistry. Chapter 3 describes
synthesis of PEO derivatives with click functionalities in the polymer backbone.
The conductivity with these materials mixed with salts is similar to data with
pure PEO, suggesting that using click chemistry in the synthesis of lithium ion
7
electrolytes is feasible. The triazole and thioether groups do not limit
conductivity.
8
REFERENCES
9
REFERENCES
1. Zhao, H. Master Thesis, 2011, MSU.
2. Beyer, M.; Lohrengel, B.; Nghiem, L. D., Membrane fouling and chemical cleaning in water recycling applications. Desalination 2010, 250 (3), 977-981.
3. Zhou, H., Brunelle, J., Moore, D., R., Zhang, L., Misner, M., J., Chen, X., Ma, M., Block copolymer membranes and associated methods for making the same. US Patent, 123033 A1, 2011.
4. Asfour, F. Ph.D Dissertation, 2004, MSU.
10
Chapter 2. Synthesis of Polyethersulfone (PES)-Based Amphiphilic Block Copolymers
1. Introduction
This chapter describes the synthesis of new polysulfone-based block
copolymers and preliminary studies on their solubility and phase-segregation
properties. To put this work in context, in this introduction I first discuss the
importance of polysulfone materials in water-treatment membranes.
Polysulfone block copolymers can serve as additives to make these
membranes more hydrophilic and reduce fouling. Thus, section 1.2 describes
block copolymers in general, and section 1.3 presents specific literature
examples of the synthesis of polysulfone-based block copolymers. In section
1.4, I provide a brief description of the self-assembly of block copolymers, and
section 1.5 of the introduction mentions a specific application of block
copolymer self-assembly, the formation of nanoporous structures. Finally,
section 1.6 discusses challenges in the self-assembly of polysulfone-based
copolymers.
1.1. Polysulfone Materials and Their Application as Water Treatment
Membranes
Polysulfone (PSf) and polyethersulfone (PES) constitute an important class
of engineering thermoplastics that is widely used to manufacture membranes
with relatively high chemical, thermal and mechanical stability. Broadly
speaking, polysulfone refers to all sulfone-containing polymers, so both
bisphenol A polysulfone and polyethersulfone (PES) are polysulfone materials.
11
In all polysulfones, but especially PES, the aromatic rings in the polymer
backbone are electronically deactivated by the adjacent sulfone (-SO2) groups.
Additionally, the repeating aromatic rings cause steric hindrance to rotation
around the polymer backbone, and both of these factors make PES unusually
stable.
Bisphenol A polysulfone or poly(oxy-1,4-phenylenesulfonyl-1,4-phenylene
oxy-1,4-phenylene(1-ethylethylidene)-1,4-phenylene) (Scheme 2.1) has a
glass transition temperature (Tg) of around 185 oC. Polyethersulfone (PES) or
poly(oxy-1,4-phenylenesulfonyl-1,4-phenylene) has an even higher Tg of 220
oC (Scheme 2.1).
1
Because of its high Tg, PES can retain dimensional stability at temperature
as high as 200 oC.
2 As a high-temperature-resistant resin, PES is also flame
retardant, certified for UL94-V0 (burning stops within 10 seconds on a vertical
specimen; drips of particles allowed as long as they are not inflamed).2
12
Scheme 2.1. Chemical Structures of Bisphenol A Polysulfone (PSf) and
Polyethersulfone (PES).
Membranes made of PES show wide pH tolerance (1 to 13); excellent
resistance to oxidants, including chlorine employed in water treatment (i.e., <
50 ppm); and stability at high temperature (operation at 75 oC and limited
exposure to temperature up to 125 oC).
3 Because of this stability, PES is
widely used to create water treatment membranes for applications such as
wastewater purification and seawater desalination (removal of salt and other
minerals from saline water).
PES shows excellent chemical and water resistance, partly because of its
hydrophobicity. However, this means that it also exhibits a low wettability.
Water contact angles on PES range from 53o to 60
o, and these values are
higher than contact angles on both cellulose (36.9o) and aromatic polyamide
(36.9o) membranes.
4 Recent research correlated low surface wettability with
increased non-specific adsorption of naturally occurring organic matter (NOM)
on the membrane.5 Such adsorption is a major cause of chronic fouling of
membranes during water treatment. Fouling causes a significant increase in
hydraulic resistance and leads to a permanent flux decline or a need for higher
transmembrane pressures.5
Blending of hydrophobic PES with hydrophilic polymers should increase
wettability and decrease fouling propensity.6 However, blends suffer from
long-term instability due to migration of the hydrophilic molecules to the
13
surface. Amphiphilic block copolymers can potentially increase hydrophilicity
and avoid such instability. The next section describes some general methods
for the synthesis of block copolymers, whereas section 1.3 gives specific
examples of the synthesis of polysulfone-based block copolymers.
1.2. Block Copolymers
The synthesis of block copolymers has been studied extensively, and
several authors reviewed this subject.7 Advances in polymer synthetic
chemistry in recent decades, especially in controlled radical polymerization,
have enabled access to a wide range of block copolymer compositions and
architectures.
In a conventional free radical polymerization, decomposition of an initiator
generates a radical that starts the polymerization of a vinyl monomer (e.g.
methylacrylate, methyl methacrylate and styrene). Because of the high
reactivity of radicals with monomers, propagation is very rapid. Since initiation
is not instantaneous, this rapid propagation makes the lengths of polymer
chains inhomogeneous. Additionally, radicals in solution undergo coupling
reactions that terminate chain growth and further broaden the molecular
weight distribution.
Attainment of narrower molecular weight distributions requires slower
propagation rates and termination reactions through controlled or living
polymerization techniques. Three criteria define such techniques: (1) fast
initiation in which the polymer chains start to propagate at the same time; (2)
14
homogeneous propagation to ensure that the chains grow at the same rate;
and (3) minimal termination. The case of zero termination corresponds to the
definition of a ‘living’ polymerization. In reality, no system is completely
“living”, but many are highly controlled. Atom Transfer Radical Polymerization
(ATRP) is one of the most common controlled radical polymerization
techniques. Scheme 2.2 shows the ATRP mechanism.8
Scheme 2.2. Reactions invovled in ATRP.8
In this scheme, PnX is the initiating alkyl halide/macromolecular species;
kact is the rate constant of activation through radical formation; kdeact is the
rate constant for the reverse reaction, which gives a dormant chain; Mtm
represents the transition metal species in oxidation state m; and L is the
metal-binding ligand. ATRP uses halide derivatives as initiators (bromo or
chloro groups), and Cu(I) is the most widely used catalyst, although other
metal species such as Ru(II), Fe(II), Cr(III), and Os(II) can also catalyze the
polymerization.9,10
Ligands (typically amine derivatives) chelate the Cu(I) to
increase its solubility in organic solvents and tune its catalytic properties.
Oxidation of the Cu(I)/L complex occurs with homo-cleavage of the carbon
halide bond to form carbon radicals, and the radical initiates the polymerization.
However, kact is typically two to four orders smaller than kdeact, so PnX serves
15
as a reservoir of radical initiators (Scheme 2.2), and the radical concentration
at any given time is low. The propagation rate is kp[Pn*][M] (kp is the
propagation rate constant, [Pn*] is the concentration of radicals, and [M]
concentration of monomers). Equally important, the termination rate is
kt[Pn*][Pn*] (kt is the termination reaction constant). Thus, the propagation rate
is first order with respect to the radical concentration, but the termination rate is
second order. The low radical concentration gives rise to a slow, controlled
first-order propagation reaction, while the second-order termination reaction is
nearly negligible.
16
Scheme 2.3. Possible architectures of copolymers synthesized from two
monomers, A and B.
Scheme 2.3 shows the common copolymer structures synthesized from two
types of repeating units, A and B. In linear polymers A and B may appear
randomly, in an alternating pattern or in blocks, and the resulting polymers are
17
termed random, alternating, and block copolymers, respectively. In some
cases, blocks containing a single repeating unit may branch out from the
polymer main chain to give a graft copolymer. If the blocks branch out from a
common location on the main chain, the structure is a star copolymer. Because
ATRP gives polymers with low polydispersity and minimal termination, it is
particularly useful for synthesizing block copolymers by sequential synthesis of
the different blocks.
Amphiphilic block copolymers contain with both hydrophobic and hydrophilic
blocks. Based on different categories of hydrophilic blocks, there are three
kinds of amphiphilic block copolymers: non-ionic copolymers, such as
poly(ethyleneoxide)-poly(propyleneoxide) (PEO-PPO), poly(ethyleneoxide)-
poly(oxybutylene) (PEO-PBO) and polyethyleneoxide-polystyrene (PEO-PS)
diblock or triblock copolymers; ionic copolymers with polyacrylic acid (PAA) or
polymethacrylic acid (PMAA); and copolymers containing monomers with
nitrogen, such as poly(2-vinylpyridine) (P2VP) and poly(4-vinylpyridine)
(P4VP), which could be quaternized to provide cationic blocks. Block
copolymer materials are attractive for application as surfactants, foam
stabilizers, flocculants, wetting agents, and dispersants. Micellization of the
amphiphilic block copolymers can solublize active drugs to increase solubility
and circulation half life.11
1.3. Polysulfone-Based Amphiphilic Copolymers
A number of studies examined the synthesis of polysulfone-based
18
copolymers to modify the properties of polysulfone while retaining aspects of
its high stability. Jo et al. prepared a polysulfone-based amphiphilic block
copolymer for potential use in a fuel cell membrane.12
Nafion (DuPont) is the
most common material for polyelectrolyte membranes in proton exchange fuel
cells, but its conductivity and mechanical stability deteriorate at high
temperature (over 100 oC). Due to its excellent thermal stability, polysulfone
might provide an attractive alternative material, although it is less chemically
stable than Nafion.
hydrophobic
hydrophilichydrophilic
CN
SO3H
p r m-r
(p, m and r are independentintegers, and m is greater than r)
m
hydrophobic block
hydrophilic block
n
SO O
OO
O
Scheme 2.4. Structure of the block copolymer synthesized by Jo.12
To prepare a polysulfone-based amphiphilic block copolymer, Jo et al.
copolymerized styrene and acrylonitrile from a polysulfone macroinitiator. They
subsequently partially sulfonated the polystyrene to provide the hydrophilic
block (Scheme 2.4). Because of the high thermal stability of polysulfone,
19
electrolyte membranes prepared from the amphiphilic block copolymer
maintained their conductivity and mechanical stability at 130 oC.
hydrophobic
hydrophilichydrophilic
hydrophobic block
n
SO O
OO
hydrophilic blocks
9
polyHEMA polyPEGMA polyDMAEMA
OO
OH
m
OO
O
m
OO
N
m
Scheme 2.5. PSf-based amphiphilic block copolymer prepared by Moore et al.
for formation of membranes.13
Moore et al. used polysulfone macroinitiators in polymerization of hydrophilic
monomers such as 2-hydroxyethyl methacrylate (HEMA), polyethylene glycol
methacrylate (PEGMA) and N, N-dimethylaminoethyl methacrylate (DMAEMA)
(Scheme 2.5).13
Synthesis occurred on a 100 g scale, and membranes made
of the synthesized copolymers showed improved hydrophilicity and open pores
that give minimum hydraulic resistance while maintaining the mechanical
strength of PES. The membranes also showed reduced fouling.
Wang et al. synthesized polysulfone-based amphiphilic ABA
copolymerS(Scheme 2.6) using the hydrophilic monomers PEGMA and
20
3-O-methacryloyl-1,2:5,6-di-O-isopropylidene -D-glucofuranose (MAIpG).14
The protected sugar moiety was acidolysized after polymerization to remove
Scheme 2.6. PSf-based amphiphilic block copolymers synthesized by Wang
for use as membrane additives.14
isopropylidenyl groups and provide the hydrophilic block. They used the
amphiphilic block copolymers as additives to improve the hydrophilicity and
resistance to Bovin Serum Albumin (BSA) adsorption of polysulfone
membranes. In another work, Yi et al. chloromethylated polysulfone
(PSf-CH2Cl, Scheme 2.7), and used the chloromethyl groups to initiate
subsequent ATRP of polyethylene glycol methacrylate (PEGMA) and produce
the amphiphilic graft copolymer.15
21
Scheme 2.7. PSf-based graft copolymer prepared by Yi.15
Scheme 2.8. PES-based graft copolymer synthesized by Yi et al.16
In a similar work, the same group synthesized a polysulfone-based graft
copolymer using Reversible Addition Fragmentation Chain Transfer (RAFT)
polymerization. In the synthesis of the PES backbone, the ratio of bis
(3-amino-4-hydroxyphenyl) sulfone and bisphenol sulfone was 2/3.16
The
amino group in the synthesized PSf was converted to a RAFT chain transfer
22
agent, which participated in RAFT polymerization with N,
N-dimethylaminoethyl methacrylate (DMAEMA) or N-isopropylacrylamide
(NIPAAm) hydrophilic monomers to give the amphiphilic graft polymers
(Scheme 2.8).
1.4. Self-assembly of Block Copolymers
When dissolved at low levels in selective solvents, block copolymers tend to
self-assemble into micelles. At even lower concentrations, there are not
enough polymers to self-assemble, so the chains adsorb at the air-water or
aqueous-organic solvent interface. When the copolymer concentration
increases, more and more polymer chains adsorb at the interface until the
concentration reaches a point where both solution and interface are saturated
with polymer chains. Upon further addition of polymer chains to the solution,
the copolymer self-assembles into micelles to reduce the free energy of the
system. The selective solvent is good for only one of the blocks in the
copolymer, so the insoluble blocks aggregate to give the core, while the
soluble blocks form the corona of the micelle. Interaction of the soluble
blocks and the solvent stabilizes the micelles.
Equation (1) expresses the free energy of micellization, ∆G,
∆G =∆H - T∆S (1)
where ∆H and ∆S are the enthalpy and the entropy of micellization. In the
micellization of block copolymers in solution, ∆S is typically negative due to
loss of entropy from localization of polymer molecules in the micelle. Moreover,
23
the solvent incompatible block is confined to the core, the solvent compatible
block is confined to the corona, and the block copolymer junction is confined to
the interfacial region between core and corona of the micelle. For micellization
of copolymer chains to be a thermodynamically favorable process, the free
energy change of the system upon micellization must decrease, i. e. ∆G<0,
and ∆H must be negative. This readily occurs because the interaction of the
nonselective block with the solvent is unfavorable.
In a molten state or in polymer solutions at high concentrations, block
copolymers can self-assemble into domains with sizes ranging from
nanometer to micrometer scales. The size and structure of the self-assembly is
governed by the polymer molecular weight, the block-size ratio and
temperature. Block copolymers may adopt a disordered/homogeneous state at
high temperature, but when the temperature decreases, the incompatibility of
the constituent blocks increases, because the influence of combinatorial
entropy decreases (T∆S decreases). At the order-to-disorder transition
temperature (TODT), block copolymers form ordered mesophase structures.
TODT depends on the volume fraction of one block, the total number of
monomers in each polymer, and the segmental interaction described by the
Flory-Huggins interaction parameter χ.17,18
24
Figure 2.1. Equilibrium morphologies in AB diblock copolymers.17
(Used from
ref 17 with permission of Copyright 2012 Annual Reviews.)
Self-consistent mean field theory describes the phase behavior of block
copolymers. As the volume fraction of the A block increases, the microdomain
changes from spheres, cylinders, to gyroid, and finally to lamellae (Figure
2.1).12
In recent years the gyroid phase has attracted attention because of its
potential application in ionic conductive materials. While the matrix provides
mechanical support, the bicontinuous gyroid phase can act as an ionically
conductive channel.19 ,20
1.5. Block Copolymers as Phase Inversion Membrane Materials
Phase-inversion has been widely used in the preparation of asymmetric
filtration membranes since the 1960s.21,22,23
(Asymmetric membranes
contain a dense surface layer on a highly porous support of the same material.)
Scheme 2.9 shows a typical phase-inversion process. Polymer materials are
dissolved in a good solvent, such as tetrahydrofuran (THF),
dimethylformamide (DMF), N-methylpyrrolidone (NMP) that is also miscible
25
with water. The concentration of the polymer is normally in the range of 20 to
35 wt% to maintain a high viscosity. The polymer solution is then cast on a
glass substrate and solvent is allowed to evaporate for a short time (10
seconds to 1 minute). Finally, the substrate is immersed in a nonsolvent bath
(typically water) at a pre-determined temperature. After oven drying, the film is
detached from the substrate.
Scheme 2.9. Protocol for making phase-inversion membranes.
The exchange between solvent and nonsolvent introduces phase separation
in the polymer layer, which leads to an asymmetric porous polymer membrane
structure. Figure 2.2 shows the morphologies of phase-inversion membranes
made from polysulfone materials. Because of the rapid solvent exchange near
the membrane surface, the thin top layer is a structure of closely packed
viscous polymer solution
cast on substrate
allow the solvent topartially evaporate
immerse in a nonsolvent bath
dry the film
26
polymeric spheres and serves as the functional layer for the separation
process. The much thicker bottom structure with large elongated voids
(macrovoids) provides the mechanical support, but little resistance to flow in
comparison to the skin layer.14
Figure 2.2. Phase inversion membranes made from PSf14
(upper left: SEM
top view, upper right: edge view, NMP solvent), and PES16
(bottom: SEM edge
view DMAc solvent), (used with permission of Elsevier from references 14 and
16, copyright )
When the membrane material is a block copolymer, the above-mentioned
phase-inversion process can lead to structures that contain uniform nanopores
in their interfacial layer. The most successful studies employed poly
(styrene)-block-poly (4-vinylpyridine) (PS-b-P4VP).24,25
This asymmetric
membrane forms in a combination of phase-inversion and block copolymer
self-assembly. In an appropriate solvent, the block copolymer self-assembles
27
into perpendicularly aligned cylinders at the membrane surface, because this
is the thermodynamic equilibrium structure. When the membrane is immersed
into the nonsolvent coagulation bath, solvent-nonsolvent exchange occurs
immediately at the membrane surface to lock in the thermodynamic equilibrium
structure (perpendicularly aligned cylinder morphology) at the interface. In
contrast, the nonsolvent migrates slowly into the interior of the membrane, and
the delayed solvent-nonsolvent exchange gives a non-equilibrium structure,
similar to that in a conventional phase-inversion membranes. The narrow
surface pore size distribution may lead to relatively sharp molecular weight
cutoffs (Figure 2.3), whereas the minimal thickness of the interfacial layer can
allow extremely high flux. In a recent publication, Peinemann and coworkers
reported a remarkable flux of 890 L m-2
h-1
bar-1
through such membranes.24
Figure 2.3. SEM images of membranes prepared by phase inversion of
poly(styrene)-co-poly(4-vinylpyridine). Peinemann’s work. Edge view (left), top
view (right). 24
(Used with permission from ref 24, Copyright 2007 Nature
Publishing Group.)
1.6. Unique Aspects of Self Assembly of Polysulfone-based Block
Copolymers
28
We synthesized ABA triblock copolymers where the B block is PES and the
A block is poly(2-hydroxyethyl methacrylate) (polyHEMA) or poly(2-hydroxy
propyl methacrylate) (polyHPMA). We note that these copolymers present
some unique features for self assembly. First, the PES block will have a
relatively broad molecular weight distribution. Most of the previous research in
block copolymer self assembly focused on model compound such as
PPO-PEO and PS-PAA because those polymers are easy to synthesize with a
narrow polydispersity index (PDI). The PDI value is the ratio of weight-average
to number-average molecular weight (Mw/Mn). With polysulfone-based
copolymers, a narrow PDI is difficult to achieve because polysulfones are
obtained via polycondensation chemistry, which leads to a PDI of around 2.
Although ATRP can give relatively monodisperse polyHEMA and polyHPMA,
the condensation polymerization of PES will lead to a more polydisperse
material. However, a recent study shows that narrow dispersity copolymers are
not required for periodic nanoscale assembly. Widin and coworkers examined
the self assembly of poly(styrene)-poly(1,4-butadiene)- poly(styrene) ABA
triblock copolymers similar in structure to those described here.26
Their ABA
triblock copolymers contained a narrow dispersity A block (Mw/Mn ≤ 1.05)
and a variable dispersity B block (Mw/Mn= 1.18−2.00). These copolymers
show the same ordered structures regardless of the polydispersity of the B
block, although the composition window for different ordered structures varies
with PDI. We expect that if the PDI of a synthesized copolymer is below 1.5,
29
one can still achieve periodic nanoscale self-assembly.
A second unique feature of PES-containing block copolymers is that PES is
more rigid than PS and other well-studied hydrophobic polymer structures in
the literature. The persistence length of this rigid polymer backbone will thus
be larger than common PS and PMMA blocks, which have has a flexible
backbone and coil structure. The extent to which rigidity will alter self-assembly
is unknown.
2. Results and Discussion
This section primarily describes the synthesis of several ABA block
copolymers where PES is the hydrophobic B block and polyHEMA or
polyHPMA serves as the hydrophilic A block. The first section describes
purification of HPMA to obtain a single isomer for formation of polyHPMA
blocks. Subsequent sections present the synthesis of PES and conversion of
PES to a macroinitiator for polymerization of HEMA or HPMA. A model
compound for the PES macroinitiator, BisphenolS-I (see below) is used to
develop an appropriate ATRP catalytic system to synthesize block copolymers.
Finally, we synthesized copolymers with a range of compositions. The new
block copolymers are characterized using nuclear magnetic resonance (NMR)
spectroscopy, gel permeation chromatography (GPC), Fourier transform
infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA) and dynamic
light scattering (DLS). Measurements of critical water content (CWC), which is
used to study the hydrophilicity of PES and synthesized block copolymers in
30
solvent/nonsolvent (water) mixtures, clearly show there is an apparent
increase of hydrophilicity for the block copolymer. NMR spectroscopy and DLS
indicate the formation of micellar structures.
2.1. Purification of Hydroxypropyl Methacrylate (HPMA) Isomers
Hydroxypropyl methacrylate (HPMA) was purchased from Acros Organics,
as an approximately 3:1 (2-hydroxypropyl methacrylate/1-hydroxypropan-2-yl
methacrylate) mixture of the primary and secondary alcohols. The secondary
alcohol (2-hydroxypropyl methacrylate) is the major product, and most
commercially available HPMA has a similar composition.
OO
OH
OO
OH
+Ph3CCl
Et3N, 50 oC,
overnight
OO
OCPh3
+O
O
OH
VacuumDistillation
OO
OH
2-hydroxypropylmethacrylate
1-hydroxypropan-2-ylmethacrylate
2-hydroxypropylmethacrylate
Scheme 2.10. Selective reaction of triphenylmethyl chloride with the primary
alcohol in hydroxypropyl methacrylate mixtures and subsequent isolationof
2-hydroxypropyl methacrylate.
31
Purification of the isomers starts with reaction of the mixture with
triphenylmethyl chloride (Scheme 2.10). The bulky triphenylmethyl group
selectively protects the primary alcohol to allow isolation of 2-hydroxypropyl
methacrylate by vacuum distillation. Triethylamine is a good base for this
reaction, and in a typical purification process, 14.4 g of the isomer mixture
gave 4.2 g of pure monomer.
32
Figure 2.4. 1H NMR 500 MHz spectra of an HPMA isomer mixture (bottom)
and purified 2-hydroxypropyl methacrylate (top) in CDCl3.
The 1H NMR spectra in Figure 2.4 show that before purification, signals from
protons on both isomers appear. After purification, only signals from
2-hydroxypropyl methacrylate are present. Peaks in the bottom spectrum
33
around 2.5 and 3.6 ppm correspond to the hydroxyl protons in the two isomers.
The upper spectrum clearly demonstrates disappearance of the signals from
1-hydroxypropan-2-yl methacrylate and the successful purification of
2-hydroxypropyl methacrylate from the isomer mixture.
2.2. Synthesis of PES with Hydroxyl End Groups
ID Monomer (mmol)
Base Solvent Temperature
(oC)
Mn/PDIc
A B C
1 20 / 20 K2CO3 DMF 150 4,500/2.1
2 20 / 20 K2CO3 DMSO 180 5,200/1.9
3 20 / 20 KF DMSO 180 3,800/1.8
4 20 / 20 K2CO3 DMSO/Toluene 160 5,500/2.0
5 20 / 20 K2CO3 Sulfolane 220 4,700/1.8
6 20 / 20 K2CO3 DMAc/Toluene 140 7,800/1.8
7 / 20 20 K2CO3 DMAc/Toluene 140 10,800/2.0d
8 / 20 20 K2CO3 DMAc/Toluene 140~170 14,700/2.1d
aMonomer A: bis(4-chlorophenyl) sulfone B: bis(4-fluorophenyl) sulfone
C: 4,4’-sulfonydiphenol
bReaction time: 24h
cDetermined using GPC with polystyrene samples.
dWe did not consider signals from large aggregates in calculating these
values.
Table 2.1. Different conditions for synthesis of PES and the molecular weights
and PDI values of the resulting polymer.a,b
34
Table 2.1 shows the different conditions used to synthesize polyethersulfone
(PES). 4,4’-sulfonylbisphenol (bisphenol S, monomer C) is reacted with
bis(4-chlorophenyl) sulfone (monomer A) or bis(4-fluorophenyl) sulfone
(monomer B) in a dipolar aprotic solvent at high temperature (up to 285 oC),
e.g., Scheme 2.11. K2CO3 or Na2CO3 generate phenate salts ‘in situ’. In a
typical poly-condensation, the highest PDI of the final polymer product is
around 2.0, but in most of the commercial products the PDI is as high as 4.0. A
possible explanation for the lower polydispersity in our polymers is that low
molecular weight oligomers are added to improve the rheology and processing
properties in the commercial formulation. Table 2.1 shows that reactions using
bis(4-fluorophenyl) sulfone give higher molecular weights than reactions with
bis(4-chlorophenyl) sulfone.
Scheme 2.11. Synthesis of hydroxyl terminated polyethersulfone (PES).
The weight-average molecular weights of the synthesized polymers (Mw)
35
are 20,000~30,000 and the PDIs are ~2 (Table 2.1). Weight average molecular
weights are always higher than number average values (Mn). Compared to
commercial PES, the synthesized PES has similar molecular weight and a
lower PDI. To ensure that the chains terminate in phenol groups, we reacted
the polymers with excess amount of 4,4’-sulfonydiphenol after chain formation
(Scheme 2.11). In this way we were eventually able to cap both ends with an
ATRP initiator and form ABA block copolymers. An SNAr mechanism is used to
describe the etherification chemistry between bisphenol sulfone and
Nu-
F-+
SO O
FF
SO O
NuF
SO O
FF Nu
Scheme 2.12. Mechanism of etherification in synthesis of PES.
bishalophenyl sulfone. The nucleophile in Scheme 2.12 represents a
bisphenolate that attacks the bishalophenyl sulfone to give an anion
intermediate, which in the final step goes through reductive elimination to yield
the ether product.27
The first step is generally quite slow and is rate
determining, so any structure that facilitates the nucleophilic attack would give
a higher reaction rate. This may explain why reactions using bis(4-fluorophenyl)
sulfone give higher molecular weights than reactions with bis(4-chlorophenyl)
36
sulfone.
2.3. Synthesis of a PES Macroinitiator and Use of a Model Compound to
Explore the ATRP Catalytic System
Scheme 2.13. Synthesis of a macroinitiator from OH-terminated PES.
To synthesize PES macroinitiator (Scheme 2.13), hydroxyl terminal groups
are allowed to react with bromoisobutyryl bromide. The resulting PES
macroinitiator bears the bromoisobutyryl structure, which can initiate
polymerization of HEMA or HPMA. Before moving on to the synthesis of block
copolymers using this macroinitiator, we performed the reaction in Scheme
2.13. The purpose of this reaction is two-fold: first, to confirm that the reaction
conditions for esterification yield an essentially quantitative reaction. In the
synthesis of PES, we used an excess of bisphenol sulfone to ensure a phenol
end group structure at both ends, but we must also convert all of these phenol
end groups to the ester structure to synthesize the ABA block copolymer.
Second, the product of the reaction in Scheme 2.14 (BisphenolS-I) served as
a model compound to explore the chemistry to polymerize HEMA and HPMA
blocks. BisphenolS-I is synthesized with two equivalents of bromoisobutyryl
bromide and one equivalent of bisphenol sulfone in acetone in less than 3
hours, and the yield of this reaction is typically higher than 97%.
Br
OBr
SO O
OHHO
SO O
OO
OBr
OBr
Et3N, Acetone+
BisphenolS-I
Scheme 2.14. Synthesis of BisphenolS-I.
Figure 2.5. 1H NMR 500 HMz spectra of bisphenol sulfone (bottom) and
BisphenolS-I (top) in DMSO-d6. The signal at 2.5 ppm is due to DMSO-d6.
38
Figure 2.5 shows the 1H NMR spectra of bisphenol sulfone and
BisphenolS-I. Upon reaction with bromoisobutyryl bromide, chemical shifts of
the aromatic protons change from 7.70 ppm (Ha) and 6.90 ppm (Hb) to 8.10
ppm and 7.45 ppm, and a new peak at 2.0 ppm corresponds to the methyl
groups of the bromoisobutyryl end group. This result shows that the conditions
for esterification of the phenol groups are nearly quantitative and should also
work for the polymer. Unfortunately, the large number of repeat units in the
polymer make direct characterization of PES derivatization by NMR difficult.
Figure 2.6. ATRP kinetic plot for polymerization of HEMA using BisphenolS-I
39
as an initiator and CuBr/PMDETA as the catalyst in DMF, the initial monomer
concentration was 2 M.
As an analogue compound for the PES macroinitiator with the
bromoisobutyryl functionality on both sides, BisphenolS-I allowed us to
explore ATRP catalytic systems for HEMA polymerization. Since the PES
macroinitiator is only soluble in polar solvents such as DMF, DMSO, DMAc and
NMP, polymerization must also occur in theses solvents. BisphenolS-I was
used to polymerize HEMA, using CuBr/PMDETA (N,N,N′,N′,N′′-pentamethyl
diethylene triamine) as a catalyst, and NMP as the solvent at 40 °C. Some
prior polymerizations of methacrylate monomers using macroinitiators
occurred at 90-110 °C, but we did not use high temperatures to avoid
auto-polymerization of the monomers. Figure 2.6 shows the polymerization
kinetics for the CuBr/PMDETA/NMP system. Polymerization occurred rapidly
during the first 30 min and then slowed suggesting significant termination of
the propagating chains. The fast polymerization rate at initial stages might be
due to the use of the CuBr catalyst, since C-Br bonds have a lower
dissociation energy than C-Cl bonds and potentially gives a faster and less
controlled ATRP kinetics.28
The low conversion of monomers is also a problem,
especially when using macroinitiators, since we desire the synthesis of block
copolymers with high hydrophilic content.
40
Figure 2.7. ATRP kinetic plot for polymerization of HEMA using ethyl
bromoisobutyrate as an initiator and CuCl/CuCl2/PMDETA as the catalyst in
NMP, the initial monomer concentration was 2 M.
To further explore ATRP of HEMA, we examined polymerization using a
simple conventional initiator, ethyl bromoisobutyrate (Figure 2.7). We
employed CuCl as a catalyst instead of CuBr, because the higher dissociation
energy of the C-Cl (relative to C-Br) bond could give slower kinetics, as
mentioned above. Additionally, 0.5 equivalents of CuCl2 were added to slow
down and control the reaction. This polymerization was conducted as a
small-scale reaction. The kinetic plot in Figure 2.7 indicates that with the
41
conventional initiator ATRP of HEMA is controlled with this catalyst system.
The final conversion of the reaction is as high as 97% after 24 hours. With a
controlled ATRP catalytic system in hand, we decide to use the model initiator
BisphenolS-I to further test the controlled character of this polymerization
chemistry. Using BisphenolS-I as the initiator, we employed a Cu(I)/Cu(II)
Figure 2.8. ATRP kinetic plot for polymerization of HEMA using ethyl
BisphenolS-I as the initiator and CuCl/CuCl2/PMDETA as the catalyst in NMP,
the initial monomer concentration was 2 M.
ratio of 1/1 to further decrease the reaction rate, considering that there are two
initiating sites for each BisphenolS-I molecule. The kinetic plot in Figure 2.8
42
shows that this reaction gives a final conversion of around 96% at 24 hours,
but it may still show a small slope decrease (some termination of
polymerization) at around 100 minutes. Nevertheless, we felt that with the high
conversion and reasonable reaction kinetics, these polymerization conditions
were sufficient to proceed with HEMA polymerization from the macroinitiator.
2.4. Polymerization from a PES Macroinitiator
Figure 2.9. ATRP kinetic plot for polymerization of HEMA using a PES
macroinitiator and CuCl/CuCl2/PMDETA as the catalyst in NMP, the initial
monomer concentration was 1.3 M.
43
The kinetic plot in Figure 2.9 shows that polymerization kinetics are well
controlled (the plot is linear) when using a macroinitiator. The reaction reaches
92% conversion after 24 hours. Ideally to get a block copolymer with a desired
hydrophilic block content, we could stop the polymerization at the time
(determined from Figure 2.9) required for sufficient conversion of the
hydrophilic monomer. In practice, we employ NMR spectroscopy to monitor the
conversion in each reaction.
(a)
Figure 2.10. 1H NMR 500 MHz spectra of (a) NMP
44
Figure 2.10 (cont’d)
(b)
(c)
Figure 2.10. 1H NMR 500 MHz spectra of (a) NMP, (b) HEMA26-PES42-
HEMA26 and (c) macroinitiator in DMSO-d6.
Figure 2.10 shows 1H NMR spectra of the polymerization solvent NMP,
45
HEMA26-PES42-HEMA26 and macroinitiator. The macroinitiator spectrum
(Figure 2.10c) shows a signal from the termini of the initiator structure (Hc), but
this peak is too weak to deduce molecular weight. Comparison of spectra (a)
and (b) shows that the small peaks at 1.9, 2.2, 2.7 and 3.3 ppm in the
copolymer spectrum correspond to residual NMP solvent. This high-boiling-
point solvent is nearly impossible to remove from theses amphiphilic
copolymers. Nevertheless, the spectrum of the copolymer (Figure 2.10b)
contains the expected characteristic signals from both PES and polyHEMA
blocks. The Ha and Hb signals stem from the aromatic protons in PES,
whereas the He peak results from the methyl groups in the polymerized
methacrylate structure These three sets of peaks are separated from other
peaks in the spectrum and allow us to quantify the block copolymer
composition. The ratio of polyHEMA repeat units to PES repeat units is simply
1/3 the area for the He peak divided by 1/4 the areas of the Ha or Hb peak. We
then used the Mn value of the PES block (determined from GPC) to calculate
an approximate composition of the copolymer.
46
Polymer Samples Scale (g)Mn of the
starting PES (GPC)
Mn
(NMR)
Mn
(GPC)
PDI (GPC)
HEMA9-PES51-HEMA9 10 11,900 14,300 19,800 1.7
HEMA13-PES42-HEMA13 14 9,650 13,000 19,600 1.6
HEMA26-PES42-HEMA26 18 9,650 16,300 23,100 1.4
HEMA22-PES34-HEMA22 15 7,800 13,600 19,200 1.4
HPMA12-PES42-HPMA12 18 9,650 13,000 21,900 1.4
HPMA26-PES42-HPMA26 12 9,650 17,100 24,900 1.5
*End group signals were too weak to determine the PES Mn value from NMR
spectra. The NMR Mn values assume that the PES molecular weight is that
determined from GPC.
Table 2.2. Block Copolymers with their Molecular Weights and PDI Values.
Table 2.2 shows all the PES-based ABA block copolymer samples
synthesized in this work, including 4 samples of polyHEMA-co-PES-co-
polyHEMA and 2 samples of polyHPMA-co-PES-co-polyHPMA. By optimizing
the ATRP catalytic system in the previous section, we synthesized the
copolymer on a scale of 10~20 g. To clarify the nomenclature of the
copolymers, PES indicates the middle block (B block) is composed of
polyethersulfone and HPMA or HEMA means that the A block is composed of
47
either polyHPMA or polyHEMA. The number after PES is number of PES
repeating units in the B block, determined from GPC analysis of the
synthesized PES samples; the number after HPMA or HEMA indicates the
repeating units in theses blocks as determined from the NMR integration data
for the copolymer. Appendices 1 to 6 contain the NMR spectra for all the block
copolymers.
2.5. GPC Analysis of HEMAn-PESm-HEMAn and HPMAn-PESm-HPMAn
Block Copolymers
Figure 2.11. Gel-permeation chromatograms of (a) PES51 and (b) the
copolymer HEMA9-PES51-HEMA9.
Figure 2.11 shows gel-permeation chromatograms curves of PES and
HEMA9-PES51-HEMA9. Curve a, which is the chromatogram of the PES
48
precursor used to synthesize HEMA9-PES51-HEMA9, shows a major peak
corresponding to Mn of 11,900. The small peak at around 5.5 min suggests a
Mn of 1,000,000, which corresponds to a small amount of aggregation of PES
polymers in DMF. Curve b, the chromatogram of HEMA9-PES51-HEMA9,
exhibits a major peak corresponding to an Mn of 19,800. Thus the Mn of the
polymer increased from 11,900 to 19,800 upon addition of the HEMA blocks.
This suggests that the molecular weight of each polyHEMA block is 3,450, but
9 units of HEMA have a molecular weight of only 1170. We used DMF as the
GPC solvent and polystyrene chains as standards, and previous studies
suggest that the molecular weights of poly-methacrylate polymers are
exaggerated by a factor of two in this GPC condition.29
This along with
possible differences in PES and HEMA9-PES51-HEMA9 aggregation may
account for the difference between the calculated GPC and NMR values for
the length of the polyHEMA blocks.
49
Figure 2.12. Gel-permeation chromatograms of (a) PES42 (b) copolymer
HEMA13-PES42-HEMA13 and (c) HEMA26-PES42-HEMA26.
HEMA13-PES42-HEMA13 and HEMA26-PES42-HEMA26 were synthesized
from the same PES precursor, which exhibits an Mn value of 9,650 based on
the GPC peak centered around 7.6 min (Figure 2.12a). This precursor polymer
also shows an aggregation peak at around 5 min in the chromatogram, and we
did not use this peak in calculating the molecular weight. The major peaks from
the unaggregated copolymers (Figure 2.12b and 2.12c) appear at smaller
elution times than for the precursor, consistent with the expected increases in
molecular weight. The copolymers also show large aggregation peaks at
smaller elution times, and surprisingly the size of the aggregation peaks
increases with the amount of HEMA in the polymer. Thus, with an increase in
the hydrophilic content, more aggregation occurs. Mn values calculated based
on the unaggregated peaks in Figure 2.12 increase from 9,650 for the PES
50
precursor to 13,000 and 16,300 for HEMA13-PES42-HEMA13 and
HEMA26-PES42-HEMA26, respectively. As mentioned above, these values
likely grossly overestimate the amount of HEMA in the polymer.
Figure 2.13. Gel-permeation chromatograms of (a). PES34 and (b). HEMA22-
PES34-HEMA22.
HEMA22-PES34-HEMA22 was synthesized from the PES with a molecular
weight of 7,800 (PES34), and has the highest hydrophilic content of any of the
polyHEMA-containing copolymer, 46.2 wt% polyHEMA. Figure 2.13 shows that
the major GPC peak for this copolymer shifts to a smaller elution time relative
to the precursor, indicating a molecular weight increase from 7,800 to 13,600.
Despite the high hydrophilic content of this copolymer, we did not observe
significant aggregate peaks, probably because of the relatively low molecular
weight of the PES.
51
Step-growth polymerizations, such as the synthesis of PES, typically yield
PDI values around 2.0. As expected, the overall PDI decreased after formation
of the copolymer (Table 2.2) because polyHEMA grown by ATRP has PDI
values near 1.0. Also, increasing the polyHEMA content lowers the PDI of the
final copolymer. 1.7 for HEMA9-PES51-HEMA9, 1.6 for HEMA13-PES42-
HEMA13, 1.4 for HEMA26-PES42-HEMA26 and 1.3 for HEMA22-PES34-
HEMA22. Equation (2) was used to correlate the PDIs of each block, with the
PDI of the entire block copolymer. 30
PDIAB=ωA2(PDIA-1)+ωB
2(PDIB-1) + 1 (2)
In this equation, PDIAB is the PDI of the copolymer, ωA and PDIA are the
weight fraction and PDI of the A block, and ωB and PDIB are the weight
fraction and PDI of the B block.
Figure 2.14. An ABA block copolymer with monodisperse A block and
polydisperse (PDI=2.0) B blocks.
52
Polymer Sample PDI from GPCCalculated PDI
via equation (3)
HEMA9-PES51-HEMA9 1.7 1.79
HEMA13-PES42-HEMA13 1.6 1.69
HEMA26-PES42-HEMA26 1.4 1.49
HEMA22-PES34-HEMA22 1.4 1.41
Table 2.3. PDIs of various copolymers as determined from GPC data or
calculated using equation (2).
Using equation (2), and assuming the polyHEMA blocks are monodisperse
(PDIA=1.0), we calculated the PDIs of the four polyHEMA-co-PES-co-
polyHEMA samples (Table 2.3). In the calculation, we used PDI values from
GPC for the PES block. The calculated and experimental results match very
well for each sample.
53
Figure 2.15. Gel-permeation chromatograms of (a) PES42, (b) HPMA12-
PES42-HPMA12 and (c) HPMA26-PES42-HPMA26.
Similar to copolymers with HEMA, Figure 2.15 shows that the
HPMA12-PES42-HPMA12 and HPMA26-PES42-HPMA26 copolymers have
increased molecular weights compared to PES, with the major peak shifted to
smaller elution times. Aggregation peaks also appear for these copolymers.
As mentioned above, GPC with polystyrene standards gives much higher
molecular weights than NMR analysis.
2.6. Infrared Spectra of the Block Copolymers
54
Figure 2.16. IR spectra of (a) PES, (b) polyHEMA and (c) HEMA22-
PES34-HEMA22.
Figure 2.176 shows IR spectra of PES, polyHEMA and the copolymer
HEMA22-PES34-HEMA22. In the spectrum of PES, sulfone groups (SO2) give
rise to strong antisymmetric (1369-1290 cm-1
) and symmetric (1170-1120 cm-1
)
stretching modes. The PES backbone contains para--substituted benzene
structures that show an absorption maximum around 817 cm-1
due to the
out-of-plane CH bending. Although the PES we prepared has phenol end
groups, there are not corresponding OH stretching bands between 3500 and
3200 cm-1
. Because the phenol only exists at the chain terminus, the small
amount of phenol groups does not give a strong signal in the IR spectrum.
In the IR spectrum of polyHEMA, the hydrogen-bonded OH stretching mode
of the hydroxyl group in HEMA repeating units gives rise to a strong broad
55
band between 3500 and 3200 cm-1
; the CH2 antisymmetric stretch appears
between 2940 and 2915 cm-1
; the strong C=O stretching band shows up near
1750 cm-1
, and the symmetric C-O-C stretch at low frequency absorbs
between 1160 and 1000 cm-1
. The IR spectrum of HEMA22-PES34-HEMA22 is
essentially a sum of the PES and polyHEMA spectra.
Figure 2.17. IR spectra of (a) HEMA9-PES51-HEMA9, (b) HEMA13-PES42-
HEMA13, (c) HEMA26-PES42-HEMA26 and (d) HEMA22-PES34-HEMA22.
Figure 2.17 shows IR spectra of the four polyHEMA-co-PES-co-polyHEMA
copolymer samples synthesized in this work. The fraction of polyHEMA in the
copolymer increases from a to d. In each sample, the spectrum contains
characteristic signal s from both PES (1369-1290 cm-1
and 1170-1120 cm-1
from sulfone groups, 817 cm-1 from para-substituted benzene structures) and
polyHEMA (strong broad band between 3500 and 3200 cm-1 from hydroxyl
56
groups, 1750 cm-1
from C=O carbonyl groups) blocks. The four spectra were
normalized using the peak at 817 cm-1
, which corresponds to the out-of-plane
CH bending on the para-substituted benzene structure in the PES block. On
going from spectrum a to d, that intensity of the broad peak between 3500 and
3200 cm-1
(OH strectch of HEMA), and the absorbance at 1750 cm-1
(C=O
stretch in HEMA) increase, reflecting increasing polyHEMA content.
Figure 2.18. IR Spectra of (a). PES, (b). polyHPMA and (c). HPMA12-PES42-
HPMA12.
Figure 2.18 presents the IR spectra of PES, polyHPMA and
HPMA12-PES42-HPMA12. Similar to polyHEMA, In the IR spectrum of
polyHPMA, the hydroxyl group gIves rise to a strong broad band between
3500 and 3200 cm-1
; the CH2 antisymmetric stretch leads to a band between
2940 and 2915 cm-1
; the C=O stretching band appears near 1750 cm-1
, and
the symmetric C-O-C stretch at low frequency absorbs between 1160 and
57
1000 cm-1
. The IR spectrum of HEMA12-PES42-HEMA12 is essentially a sum
of the PES and polyHPMA spectra as expected.
Figure 2.19. IR spectra of (a)HPMA12-PES42-HPMA12 and (b) HPMA26-
PES42-HPMA26.
Figure 2.19 shows IR spectra of the two polyHPMA-co-PES-co-polyHPMA
copolymer samples synthesized in this work. As with polyHEMA-co-PES-co-
polyHEMA, the two spectra were normalized using the peak at 817 cm-1
,
which corresponds to out-of-plane CH bending on the para-substituted
benzenes in the PES block. The intensity of the broad peak between 3500 and
3200 cm-1
(hydroxyl group in HPMA) and the C-O stretch (1750 cm-1
) are
larger for the copolymer containing more HPMA, consistent with the NMR
characterization.
2.7. TGA of the Block Copolymers
58
Figure 2.20. TGA data for PES and several polyHEMA-co-PES-co-polyHEMA
samples heated under air (samples were held at 120 oC until the weight was
constant (~ 3 hours) before heating at 10 oC/min) (a) PES, (b). HEMA9-PES51-
HEMA9, (c) HEMA13-PES42-HEMA13, (d) HEMA26-PES42-HEMA26 and (e)
HEMA22-PES34-HEMA22.
Figure 2.20 shows TGA of PES and the five polyHEMA-co-PES-co-
polyHEMA copolymers heated under air. In each case, the sample was held at
120 oC for around 3 hours before starting the heating. All polyHEMA containing
copolymers, show a three-stage weight loss. The weight loss before 250 oC
probably corresponds partly to loss of the NMP, which could not be removed
from the copolymer. In the second stage, the weight loss between 250 and 500
oC corresponds to degradation of the polyHEMA block. The final stage of
weight loss between 500 and 700 oC results from degradation of the PES block,
as the PES sample (curve a) shows major degradation only in this temperature
59
region. In all samples, the weight loss curve ends at zero weight retention,
which indicates that there is almost no residual metal catalyst (copper) in the
copolymer. The fraction of polyHEMA in the copolymers increases from b
through e, so the fraction of the weight loss that occurs from 500 to 700 oC
decreases from b through e because of the lower PES content when samples
contain more polyHEMA.
Figure 2.21. TGA data for PES, polyHEMA and polyHEMA-co-PES-co-
polyHEMA samples heated under N2 (samples were held at 120 oC until
weight was constant (~ 3 hours) before heating at 10 oC/min). (a) PES, (b)
polyHEMA, (c) HEMA9-PES42-HEMA9, (d) HEMA13-PES42-HEMA13, (e)
HEMA26-PES42-HEMA26 and (f) HEMA22-PES34- HEMA22.
Figure 2.21 shows TGA of the five polyHEMA-co-PES-co-polyHEMA
copolymers and PES heated under N2. In each case, the sample was held at
60
120 oC for around 3 hours before starting the heating scan. Curve a is the
weight loss of pure PES, which eventually carbonizes under nitrogen and has
a final weight retention of around 40 wt%. This PES sample was synthesized in
the lab and has a Mn of 10,000 and a PDI of 2.0. TGA of of pure polyHEMA
(curve b) shows a complete weight loss before 550 oC, and the major
degradation occurs between 350 and 550 oC. The polyHEMA sample was
synthesized via free radical polymerization, and GPC analysis shows Mn =
57,400 and PDI = 3.6. For the polyHEMA-co-PES-co-polyHEMA copolymers,
based on the TGA of pure PES and polyHEMA, all of the polyHEMA in the
copolymer should be gone at the end of the analysis, and the PES content
should have 40% weight retention. Accordingly, the PES content should be the
final weight retention divided by 0.4, and polyHEMA and residual solvent
should make up the rest of the polymer.
Sample polyHEMA content from
NMR polyHEMA content from
TGA*
HEMA9-PES51-HEMA9 11.0 wt% 15.4 wt%
HEMA13-PES42-HPMA13 17.0 wt% 16.7 wt%
HEMA26-PES42-HEMA26 30.0 wt% 33.3 wt%
HEMA22-PES34-HEMA22 46.2 wt% 53.0 wt%
*Calculations are described in experimental section.
Table 2.4. PolyHEMA Content in Copolymer Samples as Calculated from NMR
61
Spectra and TGA under N2.
Table 2.4 shows the compositions of the four polyHEMA-co-PES-co-
polyHEMA samples as calculated from both NMR and TGA. The results from
the two characterization techniques are quite consistent.
Figure 2.22. TGA data for PES and polyHPMA-co-PES-co-polyHPMA
samples heated under air (samples were held at 120 oC until the weight was
constant (~ 3 hours) before heating at 10 oC/min) (a) PES, (b) HPMA12-
PES42-HPMA12 and (c) HPMA26-PES42-HPMA26.
Figure 2.22 shows TGA curves of the two polyHPMA-co-PES-co-polyHPMA
copolymers and PES heated under air. As mentioned above, curve a shows a
two-stage degradation of PES. The two polyHPMA-containing copolymers
show a similar 3-stage weight loss pattern to polyHEMA-co-PES-co-
polyHEMA. In all samples, the TGA curve ends at zero weight retention, again
indicating that there is little residual metal catalyst (copper) in the copolymer
62
sample. The fraction of polyHPMA in the copolymers increases from b to c, so
the fraction of the weight loss that occurs from 500 to 700 oC decreases from b
to c because of the lower PES content when samples contain more
polyHPMA.
Figure 2.23. TGA data for PES and polyHPMA-co-PES-co-polyHPMA
samples heated under N2 (samples were held at 120 oC until weight was
constant (~ 3 hours) before heating at 10 oC/min) (a) PES, (b) polyHPMA, (c)
HPMA12-PES42-HPMA12 and (d) HPMA26-PES42-HPMA26.
Figure 2.23 shows TGA of PES, polyHPMA and polyHPMA-co-PES-co-
polyHPMA with heating under N2. Curve b shows that the weight loss of pure
polyHPMA is complete before 550 oC. The polyHPMA sample was synthesized
via free radical polymerization, and GPC analysis shows Mn = 34,646 and PDI
= 1.8. As mentioned above, PES retains 40% of its weight, presumably due to
carbonization. Thus, similar to polyHEMA-co-PES-co-polyHEMA, we can
63
determine the fraction of polyHPMA in the copolymers from the final weight
retention in the TGA.
Sample polyHPMA content from
NMR polyHPMA content from
TGA
HPMA12-PES42-HPMA12 26.3 wt% 33.5 wt%
HPMA26-PES42-HPMA26 43.3 wt% 43.0 wt%
*Calculations are described in experimental section.
Table 2.5. PolyHPMA Content in Copolymer Samples as calculated from NMR
spectra and TGA.
Table 2.5 shows the calculated compositions of the two polyHPMA-co-
PES-co-polyHPMA samples, as determined from NMR and TGA data. Again,
the results from the two characterization techniques are reasonably consistent.
2.8. Critical Water Content (CWC) Values of PES and PES-based Block
Copolymers
In one process to prepare micelles using amphiphilic block copolymers, the
copolymers are first dissolved in a good solvent for both blocks, for example N,
N-dimethylformamide (DMF), dimethylsulfoxide (DMSO), N, N-dimethyl
acetamide (DMAc) or methylpyrrolidone (NMP). In a subsequent step,
deionized water is added slowly and the quality of the resulting co-solvent for
the PES block gradually decreases. At a certain level of water, the PES blocks
start to associate/aggregate to form micelles in the solution and the solution
becomes visually turbid. This transition is abrupt, and I further stirred the
64
mixture for another 30 min to make sure the turbidity maintains. The fraction of
deionized water at which the micellization process starts is defined as the
critical water content (CWC).25,26
Sample Source Mwa PDI
Terminal
Structureb
Ultrason 2020P BASF 27,000-37,000 2.5-3.0 OMe, Cl
Ultrason 6020P BASF 46,000-55,000 3.0-4.0 OMe, Cl
Ultrason E 2020P
SR Micro BASF 45,000 3.0 OH, Cl
Veradel 3600 RP
Solvay 21,000 3.0 OH, Cl
Veradel 3000 RP
Solvay 43,000-50,000 3.0 OH, Cl
aValues from GPC characterization
bCharacterized using titration by
suppliers
Table 2.6. Commercial Polyethersulfones and their Molecular Weights, PDI
Values and Terminal Groups.
Although CWC is characteristic micellization for the block copolymers, for
pure PES, the CWC corresponds to the point where the polymer separates
from the mixture. The CWC of the hydrophobic block (PES) plays a major role
in the block copolymer micellization process. Figure 2.24 shows the
room-temperature (20 oC) CWC data for five different PES materials: Ultrason
2020P, Ultrason 6020P, Veradel 3600RP, Veradel 3000RP and home-made
PES in four different solvents (NMP, DMF, DMSO, DMAc). Table 2.6 presents
the composition of the commercial polymers, and the PES we synthesized has
65
terminal hydroxyl groups, a molecular weight (Mn) of 10,000 and a PDI of 2.0.
(a). (1) DMSO, (2) DMF, (3) DMAc, (4) NMP.
(b) (1) DMSO, (2) DMF, (3) DMAc, (4) NMP.
Figure 2.24. Room-temperature critical water content (CWC) values of
different PES materials in four solvents (NMP, DMF, DMSO, DMAc).
66
Figure 2.24 (cont’d)
(c) (1) DMSO, (2) DMF, (3) DMAc, (4) NMP.
(d) (1) DMSO, (2) DMF, (3) DMAc, (4) NMP.
67
Figure 2.24 (cont’d)
(e) (1) DMSO, (2) DMF, (3) DMAc, (4) NMP.
As Figure 2.24 shows, there is a linear relation between CWC data and the
logarithm of the polymer concentration, which can be written as equation (3)
CWC = -Alogc0 + B (3)
where c0 is the initial copolymer concentration and A and B are constants for a
specific copolymer. At the critical water content, the value of the copolymer
concentration is the critical micelle concentration if micellization occurs. Figure
2.24 shows that in each polymer sample, the order of CWC values in different
organic solvents is NMP>DMAc>DMF>DMSO. This could be explained by the
solubility parameters in Table 2.7. The solubility parameter (δ) gives a
numerical estimate of the degree of interaction between materials and is a
good indicator of solubility. Materials with similar values of δ are more likely to
be miscible.
68
Solvent δd (MPa
1/2) δ
p (MPa
1/2) δ
h (MPa1/2
) δ (MPa1/2
)
NMPa 18.0 12.3 7.2 22.9
DMFa 17.4 13.7 11.3 24.8
DMSOa 18.4 16.4 10.2 26.6
DMAca 16.8 11.5 10.2 22.7
Watera 15.5 16.0 42.4 47.9
PSu (Udel)a 19.3 0 7.0 20.3
PESb 19.6 10.8 9.2 24.2
polyHEMAc 15.1±0.7 11.9±0.3 18.8±0.4 26.9±0.5
a. Brandrup, J.; Immergut, E. H.; Grulke, E. A. Polymer Handbook, 4th
ed.,
vol. 3. New York: Wiley-Interscience; 1999.
b. Hansen, C. M. Hansen Solubility Parameters: A User’s Handbook, 2nd
ed., Boca Raton, Fla: CRC Press; 2007.
c. Caykara, T.; Ozyurek, C.; Kantoglu, O.; Guven, O. J. Polym. Sci. B:
Polym. Phy. 2002, 40, 1995-2003.
Table 2.7. Solubility Parameters of Several Solvents and Polymers at 25 oC.
There are three components that contribute to a total solubility parameter: a
dispersion force component (δd), a hydrogen bonding component (δh) and a
polar component (δp). The square of the overall solubility parameter (δ) is the
sum of the squares of the component solubility parameters.
δ2 = δd
2 + δh2 + δp
2
Table 2.7 shows the solubility parameters of solvents and polymers used in
69
this study. Both NMP (δ=22.9 MPa1/2
) and DMAc (δ=22.7 MPa1/2
) have lower
solubility parameter than PES (δ=24.2 MPa1/2
). Initially, addition of water
(δ=47.9 MPa1/2
) will increase the co-solvent solubility parameter, making it
closer to that of PES and increasing solubility of PES in the co-solvent.
However, further addition of the water will increase the solubility parameter of
the co-solvent beyond that of PES to decrease PES solubility. DMF (24.8
MPa1/2
) has a solubility parameter that is very close to PES (24.4 MPa1/2
), so
addition of water only decreases the PES solubility in DMF; DMSO (26.6
MPa1/2
) has a larger solubility parameter than PES and thus this solvent
requires the least amount of water to precipitate PES.
Figure 2.25. Room-temperature CWC values for several PES samples in NMP.
(1) Ultrason 6020P, (2) Veradel 3000RP, (3) Ultrason 2020P, (4) Veradel
3600RP and (5) home-made PES. (Each data point is an average from three
70
independent samples, and the data points often obscure the error bars.)
Figure 2.25 compares CWC values of different polymers in NMP. The CWC
values decrease in the order home-made PES>Veradel 3600RP>Ultrason
2020P>Veradel 3000RP>Ultrason 6020P. CWC depends on temperature, the
nature of the organic solvent, and polymer concentration and molecular weight.
Veradel 3600RP and Ultrason 2020P have similar molecular weights that are
smaller than those of Veradel 3000RP and Ultrason 6020P, so Veradel
3600RP and Ultrason 2020P have larger CWC values than Veradel 3000RP
and Ultrason 6020P. Most of the termini in Veradel polymers are OH, whereas
Ultrason polymers have OMe and Cl terminal groups. The larger portion of OH
end groups increase the CWC of Veradel polymers relative to Ultrason when
molecular weights are equal. Our synthesized PES has a low PDI (~2) relative
to the commercial available materials (PDI=3~4). The broad molecular weight
distribution in the commercial polymers means that a portion of the sample has
very high molecular weight and this fraction of the polymer chains should
precipitate most readily from water/organic co-solvents. Thus the CWC value
is smaller for the commercial polymers than for our PES.
71
Figure 2.26. Room-temperature CWC values in NMP for (a) PES, (b)
HPMA26-PES42-HPMA26 and (c). HEMA22-PES34-HEMA22. (Each data point
is an average from three independent samples, and the data points often
obscure the error bars.)
Figure 2.26 shows room-temperature CWC data for the pure PES,
HPMA26-PES42-HPMA26 and HEMA22-PES34-HEMA22 in NMP. Both
copolymers have higher CWC values than PES, due to the higher
hydrophilicity of the copolymers. Although HPMA26-PES42-HPMA26 has a
similar hydrophilic polymer content (43.3 wt% polyHPMA) to HEMA22-PES34-
HEMA22 (46.2 wt% polyHEMA), it has smaller CWC values than HEMA22-
PES34-HEMA22. HPMA and HEMA differ only by a methyl group, but HEMA is
a more hydrophilic monomer than HPMA.
2.9. Aggregation of Block Copolymers in Dilute Solutions—NMR and DLS
Studies
72
The previous sections show that we can successfully synthesize
polyHEMA-co-PES-co-polyHEMA and polyHPMA-co-PES-co-polyHPMA ABA
block copolymers on scales of 10-20 g. Moreover, the block copolymers
precipitate or form micelles upon addition of water to organic solvents. In the
following discussion, we use HEMA22-PES34-HEMA22 to study the copolymer
aggregation behavior in solvents that are selective for one of the blocks.
Initially, a good solvent (DMSO-d6 in NMR studies, NMP in DLS studies) for
both hydrophobic and hydrophilic blocks is dissolves the polymer, and then we
add water to induce aggregation of the block copolymer. Since PES is the
hydrophobic block, water/DMSO or water/NMP co-solvents will selectively
dissolve the polyHEMA block.
1H NMR spectroscopy can conveniently reveal aggregation. Because the
PES block aggregates while the polyHEMA remains dissolved, signals from
PES should decrease with increasing water content while signals from
polyHEMA should remain relatively constant.
73
Chemical Structure of HEMA22-PES34-HEMA22
DMSO-d6
DMSO-d6/D2O 19:1 (volume ratio)
Figure 2.27. 1H NMR 500 MHz Spectra of HEMA22-PES34-HEMA22 in
DMSO-d6/D2O co-solvents with varying amounts of water.
74
Figure 2.27 (cont’d)
DMSO-d6/D2O 9:1 (volume ratio)
DMSO-d6/D2O 4:1 (volume ratio)
Figure 2.27 shows the NMR spectra of HEMA22-PES34-HEMA22 in
DMSO-d6 or mixtures of DMSO-d6 and D2O with different volume ratios. The
peaks between 0.7 and 0.9 ppm (He) are the characteristic signals of methyl
groups in polymerized methacrylate monomers, so all of the four spectra are
normalized using this peak whose integral is set to 3.0. The two peaks at
75
7.2-7.5 ppm (Hb) and 7.8-8.1 ppm (Ha) stem from the aromatic protons in the
PES block, and each of the these peaks should correspond to 4 protons per
repeat unit.
Solvent (v/v) Integral of He
(polyHEMA)
Integral of Hb
(PES)
Integral of Ha
(PES)
DMSO-d6 3.0 2.71 2.62
DMSO-d6/D2O (19/1) 3.0 2.16 2.26
DMSO-d6/D2O (9/1) 3.0 0.75 0.84
DMSO-d6/D2O (4/1) 3.0 0.30 0.40
Table 2.8. Evolution of the 1H NMR signals from HEMA22-PES34-HEMA22
with increasing of D2O content in the DMSO-d6 solvent. See the structure in
Figure 2.27 for proton assignments. Signals were normalized to that of He.
Table 2.8 shows integrals of three sets of peaks obtained with co-solvents at
different ratios. Clearly, as the D2O content in the solvent increases, NMR
signals corresponding to the PES block decrease, presumably because the
PES block aggregates to form the core of a micelle. The semi-solid state
micelle core loses its NMR sensitivity due to magnetic gradients, dipolar
broadening, and slow relaxation in the micelle core. The hydrophilic polyHEMA
block, on the other hand, form the corona part of the micelle and stays mostly
solvated. The signal to noise ratios in the NMR spectra are similar in pure
DMSO-d6, DMSO-d6/D2O (19:1) and DMSO-d6/D2O (9:1), because the
76
copolymer is quite soluble in these three different co-solvents. However, when
the D2O content increases to 20% by volume, the copolymer become insoluble
and the signal to noise ratio in the spectrum declines. Visually the NMR
solution in the tube also becomes turbid.
DLS provides values for the sizes of aggregates in solution. Because of the
high CWC values (Figure 2.24), we selected NMP/water co-solvents to study
the aggregation behavior over a wide range of water contents.
HEMA22-PES34-HEMA22 was first dissolved in NMP, and deionized water was
added dropwise to reach desired NMP/water ratio. The solution was further
stirred for 30 min before DLS characterization.
Figure 2.28. DLS size distributions for HEMA22-PES34-HEMA22 (1 mg/mL at
25 oC) dissolved in NMP and NMP/water co-solvents with different volume
ratios.
77
Solvent
(v/v)
Radii at
Peak 1 (nm)
Volume % of aggregates
In Peak 1
Radii at
Peak 2
(nm)
Volume % of aggregates
In Peak 2
NMP 3.7 99.8% X X
NMP/water (19/1)
4.9 99.8% X X
NMP/water (9/1)
7.1 96.5% X X
NMP/water (4/1)
59.6 34.7% 2,581 65.3%
Table 2.9. DLS particle sizes and particle volume percentages for aggregates
of HEMA22-PES34-HEMA22 formed in NMP/water mixtures. The mixtures
contained 1 mg/mL HEMA22-PES34-HEMA22.
Figure 2.28 and Table 2.9 show the particle size distributions that form in
mixtures containing 1 mg/mL of HEMA22-PES34-HEMA22 in NMP/water
co-solvents. The particle size distribution in pure NMP (curve a, Figure 2.28)
shows a single peak centered around 3.7 nm. This corresponds to a fully
dissolved polymers, since NMP is a good solvent for both PES and polyHEMA
blocks. Curve b shows the size distribution when the polymer is dissolved in
NMP/water (with a 19/1 volume ratio). With this small amount of water, the
solvent mixture is still a good solvent for the copolymer, so the DLS
measurement shows a fully dissolved state with monomodal radii centered
around 4.9 nm. At a water content of 10 % by volume (curve c, Figure 2.28),
the copolymer remains solvated, but the most common particle radii increases
to 7.1 nm. As the solvent becomes poorer and some molecules begin
78
interacting, the dissolved molecule sizes increases by a factor of two on going
from pure NMP to NMP with at 10 vol% water. Below 10 vol% water, a few
aggregates with radii of 1,000-2,000 nm also exist, but they constitute less
than 5 vol% of the total aggregates. Finally when the water content reaches 20
vol% (curve d, Figure 2.28), all of the copolymer form micelles with a bimodal
size distribution. Aggregates with radii centered around 59.6 nm and 2,000 nm
account for 34.7 vol% and 65.3 vol% of the particles, respectively.
Figure 2.29. DLS size distributions for HEMA22-PES34-HEMA22 (10 mg/mL at
25 oC) dissolved in NMP and NMP/water co-solvents with different volume
ratios.
79
Solvent
(v/v)
Radii at
Peak 1 (nm)
Volume % of aggregates
In Peak 1
Radii at
Peak 2 (nm)
Volume % of aggregates
In Peak 2
NMP 3.6 99.8% X X
NMP/water (19/1)
4.0 100% X X
NMP/water (9/1)
5.9 96.3% X X
NMP/water (4/1)
56.3 100% X X
Table 2.10. DLS particle sizes and particle volume percentages for aggregates
of HEMA22-PES34-HEMA22 formed in NMP/water mixtures. The mixtures
contained 10 mg/mL HEMA22-PES34-HEMA22.
Figure 2.29 and Table 2.10 show the particle size distributions that form in
mixtures containing 10 mg/mL of HEMA22-PES34-HEMA22 in NMP/water
co-solvents with different volume ratios. Even at this polymer concentration,
the copolymer is fully dissolved in pure NMP solvent and NMP with 5 vol% and
10 vol% water. The particle sizes are essentially the same as in mixtures with 1
mg/mL HEMA22-PES34-HEMA22 (compare Tables 2.9 and 2.10). Finally when
the water content reaches 20 vol% (curve d, Figure 2.29), the particle radii
center around 56 nm. We are not sure why the higher polymer concentration
leads to a monomodal size distribution while the 1 mg/mL solution shows a
bimodal size distribution in 20 vol% water. The higher polymer concentration
may lead to a higher concentration of micelles, which overwhelms the signals
from a few large aggregates.
80
Figure 2.30. DLS size distributions for HEMA22-PES34-HEMA22 (30 mg/mL at
25 oC) dissolved in NMP and NMP/water co-solvents with different volume
ratios.
Solvent
(v/v)
Radii at
Peak 1 (nm)
Volume % of aggregates
In Peak 1
Radii at
Peak 2 (nm)
Volume % of aggregates
In Peak 2
NMP 2.9 100% X X
NMP/water (19/1)
2.8 100% X X
NMP/water (9/1)
5.8 94.5% X X
NMP/water (4/1)
61.3 100% X X
Table 2.11. DLS particle sizes and particle volume percentages for aggregates
of HEMA22-PES34-HEMA22 formed in NMP/water mixtures. The mixtures
contained 30 mg/mL HEMA22-PES34-HEMA22.
Figure 2.30 and Table 2.11 show the particle size distribution in mixtures
81
containing 30 mg/mL of HEMA22-PES34-HEMA22 in NMP/water co-solvents
with different volume ratios. The size distributions are essentially the same as
those with 10 mg/mL HEMA22-PES34-HEMA22, although the radii are a little
smaller with 5 vol% water. Most notably, regardless of the copolymer
concentrations (1 mg/mL, 10 mg/mL or 30 mg/mL), the aggregated state with
20 vol% water content contains micelles with a radii around 60 nm.
3. Conclusion
ABA block copolymer samples were synthesized on of 10~20 g scale,
including 4 samples of polyHEMA-co-PES-co-polyHEMA and 2 samples of
polyHPMA-co-PES-co-polyHPMA. Using a model compound 4,4'-sulfonylbis
(4,1-phenylene) bis(2-bromo-2-methyl-propanoate) as initiator, we selected
CuCl/CuCl2/PMDETA in NMP as the catalytic system for the polymerization of
HEMA and HPMA monomers from PES macroinitiators. FT-IR spectra, TGA
and 1H NMR spectra show successful synthesis of these block copolymers.
Critical Water Content (CWC) studies demonstrate that the hydrophilicity of
synthesized copolymers increases with the amount of polyHEMA or polyHPMA
in the block copolymers as expected. Both DLS and 1H NMR studies show that
addition of non-solvent (water) to the copolymer solution causes aggregation
of the block copolymer, particularly the PES block. DLS indicates that with 20
vol% water micellar the aggregates have radii of 60 nm, regardless of the
copolymer concentration. Such copolymers may prove useful in modification of
polysulfone membranes.
82
4. Experimental Section
4.1. Materials
Phthalimide, potassium derivative (500 g, 99%, Acros Organics),
triethylamine (J. T. Baker), N, N, N’, N’, N’’-pentamethyldiethylenetri amine
(PMDETA, Aldrich, 99%), 4-fluorophenyl sulfone (100 g, 99%, Acros Organics),
4, 4’-sulfonyldiphenol (500 g, 98%, Aldrich), bis(4-chlorophenyl) sulfone (500 g,
98%, Aldrich), α-bromoisobutyryl bromide (500 g, 98%, Aldrich), N,
N-dimethylacetamide (2.5 L, 99%, Alfa Aesar), 1-methyl-2-pyrrolidinone (4 L,
ACS grade, 99.0+%, Alfa Aesar), postassium carbonate (500 g, ACP
Chemicals), 4-(dimethylamino) pyridine (100 g, 99% prilled, Aldrich), sulfolane
(500 mL, Kodak) and pyridine (500 mL, ACS grade ≥99%, CCI Chemical) were
used as received. Cu(I)Br (99.999%, Aldrich) was purified using a saturated
aqueous NaBr solution. Hydroxypropyl methacrylate (1 kg, 97+%, mixture of
isomers, stabilized, Acros Organics), 2-Hydroxyethyl methacrylate (500 mL,
200-220 ppm monomethyl ether hydroquinone as inhibitor, Aldrich, 97%) were
passed through a basic alumina column before use. ULTRASON E 6020P
(100 g), E 2020 P (100 g) and 2020P SR Micro (100 g) were received as free
samples from BASF. Veradel 3000 RP and Veradel 3600 RP were received as
free samples from Solvay Specialty Polymers. Aluminum oxide (1 kg, activated,
basic, ~150 mesh, 58 Å, Aldrich) was heated in an oven overnight at 120 oC for
activation.
4.2. Characterization
83
1H NMR and
13C NMR spectra were collected using a Varian UnityPlus-500
spectrometer using the residual proton signals from the solvent as the
chemical shift standard. Thermogravimetric analysis (TGA) were carried out in
air or under N2 using a Perkin-Elmer TGA 7 instrument at a heating rate of 10
oC/min. Samples were held at 120
oC until the weight stabilized (~3 h) before
starting the heating process. FTIR spectra were collected with a Mattson
Galaxy 300 spectrometer. FTIR samples were made by mixing the polymer
with KBr and forming pellets. DLS studies were carried out on a Malvern
Zetasizer Nanoseries ZEN3600 instrument at 30 oC.
Standards and Conditions of Gel Permeation Chromatography (GPC)
Analysis
This GPC instrument contains Water 1515 Isocratic HPLC Pump, Water 717
Plus Autosampler, Waters 2414 Refractive Index Detector and Water 2487
Dual λ Absorbance Detector. This instrument uses DMF as solvent and PLgel
10 μm mixed-B as column, 70 oC at column and 50
oC at RI detector. DMF
was used as the eluting solvent at a flow rate 1 mL/min, and monodisperse
polystyrene standards were used to calibrate the molecular weights. The
concentration of the polymer solutions used for GPC measurements was 1
mg/mL.
84
Standard
PSI
Elution time (min) 6.3 7.1 7.7 8.4
Molecular weight (Mn) 401,340 45,730 12,860 2,727
PSII
Elution time (min) 5.9 6.8 7.4 8.3
Molecular weight (Mn) 931,780 95,800 24,150 3,680
Table 2.12. Polystyrene standards used to calibrate the results of GPC in
DMF.
The molecular weight and PDI of each polymer sample were determined
by GPC. Two sets of polymer standards, PSI and PSII, were employed and
results are shown in Table 2.12. The effective calibration range for GPC
analysis is between 5.9 min (Mn of 931,780) and 8.4 min (Mn of 2,727).
Calculation of polyHEMA content in Copolymers Using TGA and NMR
Data
The polyHEMA content from TGA was calculated using Equation (4),
(4)
where W120~300 is the weight loss between 120 and 300 oC (we assume this
mostly corresponds to the unremoved solvent in the copolymer sample) and
Wretention is the final weight retention of the sample. The value of Wretention
should exclusively come from the PES block, since pure PES has a weight
retention of around 40%, whereas polyHEMA and polyHPMA show no weight
85
retention at the end of TGA.
Based on integration of the proton peaks in NMR, we obtained polyHEMA or
polyHPMA and PES contents in the copolymer.
Scheme 2.15. Characteristic protons for calculation of copolymer composition
from NMR spectra.
As shown in Scheme 2.15, to calculate polyHEMA content from 1H NMR, we
compared signals from protons in the methyl groups from methacrylate (Ha, 3
protons per repeating units, 0.7~0.9 ppm), with signals from the aromatic
protons at the ortho position to sulfone group (Hb, 4 protons per repeating unit,
7.4~7.5 ppm). Based on integrations of these two sets of peaks, polyHEMA
content could be calculated according to equation (5).
(5)
Where IHa is the integral of NMR peaks at 0.7-0.9 ppm (the molecular weight of
the HEMA repeating unit is 130 g/mol) and IHb is the integral of the NMR peak
at 7.4-7.5 ppm (the molecular weight of the PES repeating unit is 232 g/mol).
Calculation of polyHPMA content in Copolymers Using TGA and NMR
Data
86
The polyHPMA content from TGA was calculated using Equation (4). Similar
to polyHEMA-containing copolymers, NMR could also be used to obtain the
polyHPMA content.
Scheme 2.16 Characteristic protons for calculation of copolymer composition
from NMR spectra.
As shown in Scheme 2.16, polyHPMA gives signals from methyl groups (Ha)
from methacrylate at 0.7-0.9 ppm, as well as from the side-chain methyl group
(Ha’) at 0.9-1.2 ppm. The integration of the combined peaks corresponds to 6
protons. We compared this integral with that for the aromatic protons at the
ortho position (Hb) to the sulfone group (4 protons per repeating unit, 7.4-7.5
ppm). Based on integrations of these sets of peaks, we calculated the
polyHPMA content according to equation (6).
(6)
IHa+Ha’ is the integral of the NMR peaks from 0.7-1.1 ppm (the molecular
weight of the HPMA repeating unit is 144 g/mol) and IHb is the integral of the
NMR peak at 7.4-7.5 ppm (the molecular weight of the PES repeating unit is
232 g/mol).
87
Synthesis of PES with Hydroxyl End Groups. Bisphenol sulfone (26.00 g,
0.104 mol) and bisfluorophenyl sulfone (26.92 g, 0.104 mol 1:1 molar ratio)
were added to a 500 mL 3-neck flask charged with N, N-dimethylacetamide
(240 mL) and toluene (100 mL). Potassium carbonate (2 equivalents, 0.21 mol)
was added, and then the solution was purged with nitrogen for 30 min. The
reaction was heated to 145 °C, and a Dean-Stark trap attached to the flask
removed residual water from the reactor. After 12 hours at 145 °C, bisphenol
sulfone (1 g, 4 mmol) was added to the solution to cap the polymer with
phenolic groups, and after an additional hour the polymer was precipitated by
addition into 4M HCl. The white precipitate was dispersed in boiling methanol
(350 mL) for 4 hours to extract residual monomer and salts from the polymer.
The polymer was recovered by filtration, and the extraction was repeated with
fresh methanol. After drying under vacuum at 60 °C overnight, the product was
a white fine powder, and 48 g of product was isolated (99% yield).
Synthesis of the PES Macroinitiator. Polyethersulfone (50 g, 5 mmol end
groups, calculated using molecular weight from GPC assuming hydroxyl end
groups) was dissolved in a mixture of DMF/DMSO (400 mL, 1:1 volume). After
the polymer was dissolved, 20 equivalents of triethylamine (10.1 g, 0.1 mol)
and bromoisobutyryl bromide (22.9 g, 0.1 mol) were added at 0 °C. The
solution was heated to 60 °C and stirred with a mechanical stirrer for 24 hours.
Upon addition to 4 M aqueous HCl, the macroinitiator precipitated as a gel.
After poring off the solvent, the product was immersed in 300 mL boiling
88
methanol (sometimes more than once), and after 4h, the gel-like material
solidified. The solid material was broken into small particles, and methanol
extraction was performed two times using a Soxhlet extraction setup. After
the final wash, the product was a fine light yellow powder. The product was
dispersed in 400 mL deionized water at 60 °C and vigorously stirred for 1 h
before filtration, this dispersion-filtration process was repeated twice before the
solid was dried under vacuum at 60 °C overnight.
Synthesis of 4,4'-sulfonylbis(4,1-phenylene) bis(2-bromo-2-methyl-
propanoate) (BisphenolS-I). In a 100 mL round bottom flask, 2.55 g
bisphenol sulfone (0.01 mol) and 2.1 g triethylamine (0.021 mol) were added to
50 mL dry acetone. The flask was put on an ice bath to give a solution
temperature of around 0 °C. Bromoisobutyryl bromide (2.7 mL, 0.022 mol) was
added to the solution slowly through a septum (typical addition time is around 5
min). Large amounts of white/light yellow salts formed in the course of addition.
After the addition, the ice bath was removed and the solution was allowed to
warm to room temperature. After 2 h at room temperature, 50 mL of
deionized water was added to dilute the reaction solution, and the product was
extracted with dichloromethane (3 x 40 mL). The combined dichloromethane
layer was washed with deionized water (3 x 30 mL), dried with magnesium
sulfate, and the solvent was removed using rotary evaporation. The white solid
was dried in vacuum to give 5.2 g (96% yield).
Purification of 2-Hydroxypropyl Methacrylate. A 200-mL round bottom flask
89
was charged with 14.4 g commercial hydroxypropyl methacrylate isomer
mixture (0.1 mol), 27.8 g trityl chloride (0.1 mol), 10.1 g triethylamine (0.1 mol)
and 300 mL acetone. The solution was heated to 50 °C in an oil bath and
allowed to react overnight. Solvent and residual triethylamine were removed
by rotary evaporation, and vacuum distillation at 90 °C at 80 mtorr gave the
unreacted secondary alcohol isomer (4.2 g, yield 29.2%).
Synthesis of ABA block copolymers: polyHEMA-co-PES-co-polyHEMA.
In a 250 mL Schlenk flask, the PES macroinitiator (15 g, 1.5 mmol), HEMA (20
g, 0.154 mol) and PMDETA (0.60 mL, 2.9 mmol) were dissolved in NMP (120
mL). (The stirred mixture occasionally required heating to obtain a
homogeneous solution.) After two freeze-pump-thaw cycles, the flask was
refilled with nitrogen, CuCl2 (0.108 g, 0.8 mmol) was added and the solution
was stirred until the Cu species dissolved. After two freeze-pump-thaw
cycles, the flask was refilled with nitrogen and CuCl (0.078 g, 0.8 mmol) was
added to the flask under N2. The flask was heated in a 40 °C oil bath. The
reaction was monitored by 1H NMR and when the polymerization reached the
desired HEMA conversion, the solution was opened to the air to quench
polymerization reaction. The polymer was precipitated by addition of the
solution into 300 mL of saturated disodium ethylenediaminetetraacetate (EDTA)
solution, and the copolymer was recovered as a fine powder. Suction filtration
required 5-6 hours to recover the product. The air-dried product was dissolved
in DMSO, precipitated in water, and after a second precipitation from DMSO,
90
the polymer was dried under vacuum at 90 °C for 24 h. Synthesis of
polyHPMA-co-PES-co-polyHPMA occurred similarly.
Free Radical Polymerization of Hydroxyethyl Methacrylate (HEMA). A
Schlenk flask was charge with 15 mL dry THF, 4 g of HEMA (0.031 mol) and
0.43 g azobisisobutyronitrile (2.6 mmol). After one freeze-pump-thaw cyle, the
flask was put onto a 70 °C oil bath. After an overnight reaction, NMR
spectroscopy of the reaction solution showed that the conversion was 100%,
and the flask was opened to air to quench the reaction. PolyHEMA precipitated
onto the bottom of the flask, and the solid product was dried under vacuum at
70 °C. 3.56 g product was recovered (90% yield).
91
APPENDIX A
92
Appendix A1. 1H NMR 500 MHz spectrum of HEMA9-PES51-HEMA9 in
DMSO-d6.
93
Appendix A2. 1H NMR 500 MHz spectrum of HEMA13-PES42-HEMA13 in
DMSO-d6.
94
Appendix A3. 1H NMR 500 MHz spectrum of HEMA26-PES42-HEMA26 in
DMSO-d6.
95
Appendix A4. 1H NMR 500 MHz spectrum of HEMA22-PES34-HEMA22 in
DMSO-d6.
96
Appendix A5. 1H NMR 500 MHz spectrum of HPMA12-PES42-HPMA12 in
DMSO-d6.
97
Appendix A6. 1H NMR 500 MHz spectrum of HPMA26-PES42-HPMA26 in
DMSO-d6.
98
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99
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22. Smolders, C. A.; Reuvers, A. J.; Boom, R. M.; Wienk, I. M., Microstructures in phase-inversion membranes .1. formation of macrovoids. Journal of Membrane Science 1992, 73 (2-3), 259-275. 23. Amirilargani, M.; Mohammadi, T., Synthesis and characterization of asymmetric polyethersulfone membranes: effects of concentration and polarity of nonsolvent additives on morphology and performance of the membranes. Polymers for Advanced Technologies 2011, 22 (6), 962-972. 24. Peinemann, K. V.; Abetz, V.; Simon, P. F. W., Asymmetric superstructure formed in a block copolymer via phase separation. Nature Materials 2007, 6 (12), 992-996. 25. Nunes, S. P.; Sougrat, R.; Hooghan, B.; Anjum, D. H.; Behzad, A. R.; Zhao, L.; Pradeep, N.; Pinnau, I.; Vainio, U.; Peinemann, K. V., Ultraporous films with uniform nanochannels by block copolymer micelles assembly. Macromolecules 2010, 43 (19), 8079-8085. 26. Widin, J. M.; Schmitt, A. K.; Schmitt, A. L.; Im, K.; Mahanthappa, M. K., Unexpected Consequences of block polydispersity on the self-Assembly of ABA triblock copolymers. Journal of the American Chemical Society 2012, 134 (8), 3834-3844. 27. Percec, V.; Clough, R. S.; Grigoras, M.; Rinaldi, P. L.; Litman, V. E., Reductive dehalogenation versus substitution in the polyetherification of 4,4'-dihalodiphenyl sulfones with bisphenolates. Macromolecules 1993, 26 (14), 3650-3662. 28. Tang, W.; Kwak, Y.; Braunecker, W.; Tsarevsky, N. V.; Coote, M. L.; Matyjaszewski, K., Understanding Atom transfer radical polymerization: Effect of ligand and initiator structures on the equilibrium constants. Journal of the American Chemical Society 2008, 130 (32), 10702-10713. 29. Xia, J.; Matyjaszewski, K., Controlled/“living” radical polymerization. atom transfer radical polymerization using multidentate amine ligands. Macromolecules 1997, 30 (25), 7697-7700. 30. Lynd, N. A.; Meuler, A. J.; Hillmyer, M. A., Polydispersity and block copolymer self-assembly. Progress in Polymer Science 2008, 33 (9), 875-893.
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Chapter 3. Use of Nanoparticles and Click Chemistry in the Development of Single-ion Conductors for Lithium Ion Batteries
This chapter describes research aimed at developing single-ion conductors
for lithium ion batteries. The introduction first discusses why single-ion
conductors are important for decreasing concentration polarization and related
voltage losses during battery discharge. Subsequently, I first present work on
nanoparticles coated with immobilized anions as part of single-ion conductors.
This work follows up previous studies by Fadi Asfour and shows that
nanoparticles with grafted polyanions have a higher lithium conterion weight
fraction than nanoparticles coated with only monolayers of anion. However,
because the conductivity of these nanoparticle-PEO electrolytes is not high
enough for battery applications, subsequent work aims toward using click
chemistry to modify PEO directly and create single-ion conductors. These
studies show that the presence of triazole or thioether groups does not limit
conductivity. Thus, click chemistry may provide a useful method for introducing
immobile anions in PEO to create single-ion conductors.
1. Introduction- Ion Conduction in Lithium Ion Batteries
In discharge of a lithium ion battery, electrons flow from the anode to the
cathode through the external circuit, while inside the cell, lithium cations
formed at the anode migrate to the cathode and intercalate into the cathode
material with reduction at the cathode (Figure 3.1). The electrolyte usually
contains a lithium salt dissolved in a solvent, and ideally Li+ ions are the only
current carriers in this region. When anions carry a significant fraction of the
103
current, concentration polarization occurs, and the battery loses voltage.1
Figure 3.1. Schematic diagram of a lithium ion battery containing a metal
oxide cathode and a graphite anode. The figure also shows redox reaction
during discharge.
Figure 3.2 illustrates the concentration polarization. At the anode, only part
of the Li+ formed by oxidation migrates away to carry current, so Li
+
accumulates. Additionally, anions migrate toward the anode and collect there.
At the cathode, more Li+ is intercalated with reduction than can migrate to the
cathode due to current, so Li+ is depleted. Anions migrate away from the
cathode and are also depleted in this region. These accumulation and
depletion zones decrease the potential drop at the cathode-solution interface
104
and increase the potential drop at the anode-solution interface to decrease the
battery voltage. If the discharge is slow enough, diffusion will help dissipate the
concentration polarization, but at fast discharge, concentration polarization is a
serious problem. Moreover, the low conductivity in the depleted region near the
cathode increases the ohmic potential drop, which leads to heating and an
additional loss of battery voltage. The effective voltage during discharge is V
(cell voltage) - Vp (polarization voltage), and the voltage needed to charge the
cell is V+Vp. Of course, power output is directly proportional to discharge
voltage.
Figure 3.2. Concentration polarization during discharge of a lithium ion battery.
The lithium ion transference number (tLi+) is the fraction of current in solution
carried by Li+. For electrolytes with only one cation and one anion, the sum of
the cation and anion transference numbers must equal 1. Typical Li+
transference numbers in PEO-based electrolytes range from 0.2 to 0.4 (Table
3.1), showing that the anion is the dominant current-carrying species. Thus,
concentration polarization during discharge may be severe as more Li+ ions
105
form at the anode than can migrate away, and more Li+ enters the cathode
than migrates there. Electrolytes with Li+ transference numbers close to 1 are
highly desirable for decreasing concentration polarization.
Lithium Salt Polyether
(or solvent)O/Li ratio
dTemperature
(oC)
tLi+
LiClO4 PEO1000a 20 30 0.23
LiCF3SO3 PEO1000a 24 30 0.21
LiBF4 PEO500b 20 70 0.32
LiPF6 PC/EC/DMCc 1 M 25 0.38±0.04
aPoly(ethyleneoxide) with Mn of 1,000.
bPoly(ethyleneoxide) with Mn of 500.
cPC, propylene carbonate; EC, ethylene carbonate; DMC, dimethyl
carbonate; 1:1:1 is volume ratio.
donly the ether oxygens in PEO are considered.
Table 3.1. Lithium transference numbers for several lithium salts in battery
solvents.1
One way to obtain single-ion (Li+) electrolytes is to attach anions to
polymers through covalent bonds, so the Li+ counterion is the only mobile ion.
As long as all anions are tethered to the polymer and immobile, tLi+ should be
unity.2,3,4 Another method for immobilizing anions involves grafting to
nanoparticles. In this work I began following up on our previous studies with
nanoparticles coated with monolayers of anions. To increase the amount of Li+
106
per nanoparticles, I grafted polyanions to the particles. Unfortunately, the
conductivity of polyelectrolytes containing these modified particles was
impractically low, so I also began examining methods to introduce anions
directly into PEG.
2. Results and Discussion
2.1. Single-ion Conductors Containing Nanoparticles with Immobilized
Anions.
Scheme 3.1. Monolayer modified silica nanoparticle Si-C5NTfLi (silica
nanoparticle derivatized with lithiated N-pentenyl triflouromethane
sulfonamide).5
Scheme 3.1 shows the monolayer-modified nanoparticles (Si-C5NTfLi) that
our group mixes with PEO to create single-ion conductors. Fadi Asfour initially
developed and studied these particles.5 We employ silica nanoparticles with
diameters of around 12, and a 5-carbon spacer separates the trifluoromethane
sulfonamide from the nanoparticle surface.5 To prepare electrolytes, we
disperse the nanoparticles in polyethylene oxide dimethylether (Mw=500 g/mol)
(PEGDME-500). Since the nanoparticles and hence the anions are immobile,
Li+ is the only species that conducts current.
107
Scheme 3.2. Method for determining the Li+ content of PEO-based
electrolytes.
In following up on previous studies of these conductors, I first determined
the amount of Li in the modified nanoparticles. Quantitative analysis of the
metal content in the TGA residue by using inductively coupled plasma optical
emission spectrometry (ICP-OES) gives an estimate of the number of anions
bound to the nanoparticles. The lithium in the residue should be Li2O or
Li2CO3, and both are water soluble. The TGA residue was stirred in deionized
water for 12 h, and filtered prior to the ICO-OES analysis. The combined
TGA/ICP-OES analysis of the modified particle shows a lithium content of 1.2 x
10-3
g Li/g particles. We prepared electrolytes with various O/Li ratios by
dispersing the Si-C5NTfLi in PEGDME-500, and Table 3.2 presents the O/Li
ratio in the electrolytes.
108
O/Li ratioa 425 320 230 185
Particle Content (wt%) 18.5 23.6 30.0 35.0
Conductivity at 30 oC (S/cm) 1.3x10
-68.4x10
-71.2x10
-6 5.3x10
-7
aThe O/Li ratio does not include any O from the Si-C5NTfLi particles.
Table 3.2. Particle weight percentages and O/Li for electrolytes prepared from
Si-C5NTfLi dispersed in PEGDME-500.
Figure 3.3. Temperature-dependent conductivity of electrolytes containing
different fractions of Si-C5NTfLi dispersed in PEGDE-500. These results were
obtained by Fadi Asfour, and I repeated some of the measurements.5
Figure 3.3 shows the temperature-dependent conductivities of electrolytes
with different particle contents. The conductivities at 30 oC (1000/T=3.3) are
around 10-6
S/cm, and conductivity increases by less than an order of
109
magnitude on gong from 30 oC (1000/T=3.3) to 80
oC (1000/T=2.83). These
low conductivities may stem from the low lithium content in the electrolyte
materials. As Table 3.2 shows, the O/Li ratio is between 200 and 400 for all the
electrolytes. Increasing the particle content adds Li+ to the electrolyte, but
does not change the conductivity by more than a factor of 3. At high particles
contents, the lack of ionic conductivity through the interior of the nanoparticles
may decrease the overall conductivity. Thus improvements in conductivity will
require increases in the amount of Li per g of particle.
2.2. Single-ion Conductors Prepared Using Nanoparticles Modified by
Grafting of Polyanions
Scheme 3.3. Silica nanoparticles prepared by grafting lithiated poly
(trifluoromethane sulfonic aminoethyl-methacrylate) (Si-TfMALi) from the
surface.1
Scheme 3.3 shows our strategy to increase the Li content in modified
silica nanoparticles. Growth of a poly(trifluoromethane sulfonimide aminoethyl-
methacrylate) (TfMALi) from the particles yields many sites for Li+ counterions.
(I describe the synthesis of these particles in my MS thesis.1) TGA-ICP
characterization of the grafted particles shows a lithium content of 2.0 x 10-2
g
Li/g Si-TfMALi particles. Compared to the 1.2 x 10-3
g Li/g Si-C5NTfLi,
110
Si-TfMALi contains an order of magnitude more Li per g of particles. Mixing
Si-TfMALi particles with PEGDME-500 thus yields high O/Li ratios compared
to those in dispersions of Si-C5NTfLi (compare Tables 3.2 and 3.3).1
O/Li ratioa 16 32 64 96
Particle Content (wt%) 33.2 19.9 11.1 7.7
Conductivity at 30 oC (S/cm) 7.5x10
-73.2x10
-62.1x10
-6 3.1x10
-7
aThe O/Li ratio does not include any O from the Si-TfMALi particles.
Table 3.3. Particle weight percentages and O/Li ratios for electrolytes
prepared from Si-TfMALi dispersed in PEGDME-500.
Figure 3.4. Temperature-dependent conductivity of electrolytes containing
different fractions of Si-TfMALi dispersed in PEGDE-500. The various fractions
of particles (see Table 3.3) lead to the different O/Li ratios shown in the figure.1
111
Figure 3.4 shows the temperature-dependent conductivities for
dispersions of Si-TfMALi in PEGDME-500 as a function of the O/Li ratios in the
dispersions. The conductivities, which are extracted from impedance
spectroscopy data, are roughly linear with 1/T, consistent with thermally
activated transport. Conductivities at 30 oC are on the order of 10
-6 S/cm,
similar to values with Si-C5NTfLi/PEGDEM-500.
Figure 3.5. Temperature-dependent conductivity for (a) Si-C5NTfLi at O/Li 425
and (b) Si-TfMALi at O/Li 32, both samples contain ~19 wt% modified particles.
Figure 3.5 compares temperature-dependent conductivities for
Si-C5NTfLi/PEGDME-500 (O/Li=425) and Si-TfMALi/PEGDME-500 (O/Li=32)
dispersions. Both composite electrolytes have particle fractions of around 19
wt%, but the polyelectrolyte-modified particles contain much more Li. The
system with a monolayer of anions on the particles (Si-C5NTfLi/PEGDME-500)
112
exhibits a 2-fold increase in conductivity on going from 30 to 80 °C. At 30 °C
the polyectrolyte system, Si-TfMALi/PEGDME-500, has a conductivity similar
to that of Si-C5NTfLi/PEGDME-500 (a difference of about 0.5 log units), but at
80 °C, the conductivity of Si-TfMALi/PEGDME-500 is a full order of magnitude
higher. Scheme 3.4 presents a proposed explaination for these results.
Li+Li+
Li+Li+
Li+
Li+Li+ Li+
Li+
Li+
Li+ Li+
Li+
Li+Li+Li+
Li+
Li+Li+
N SO
OCF3
1.3 x 10-6 S/cm at 30 oC 2.8 x 10-6 S/cm at 80 oC
3.2 x 10-6 S/cm at 30 oC 2.9 x 10-5 S/cm at 80 oC
Li+Li+
Li+Li+
Li+
Li+Li+ Li+
Li+
Monolayer
Grafted polymer
Li+
Li+
Li+
Li+Li+
Li+
Li+Li+
=
Scheme 3.4. Proposed qualitative conformations of monolayer Si-C5NTfLi
(top) and multilayer Si-TfMALi (bottom) at 30 oC and at 80
oC.
The conformation of the monolayer does not change significantly with
increasing temperature, so the conductivity of Si-C5NTfLi/PEGDME-500
increases marginally on going from 30 to 80 °C. At 80 °C, the polyTfMALi
chains are not highly soluble in PEGDME-500, so only the exterior lithium ions
113
are accessible to the PEGDME-500 matrix for conductivity. Increasing the
temperature increases the solubility or mobility of the polyelectrolyte in
PEGDME-500, and more Li+ becomes available to the matrix for conductivity.
Thus at 80 oC, the conductivity of Si-TfMALi/PEGDME-500 reaches 3x10
-5
S/cm. The conductivity of this system is an order of magnitude lower than the
values of typical electrolytes used in Li ion batteries,6 but the increase in
conductivity at high temperature suggests that if more Li+ is accessible to
PEGDME-500, we may be able to create competitive single-ion conductors.
2.3. Towards Click Chemistry for Synthesizing Single-ion Conductors
with a High Density of Li+ in PEO
To increase the concentration of Li+ in poly(ethyleneoxide) (PEO) while still
maintaining single-ion conductivity, we aim to eventually graft anionic groups
directly to the PEO backbone (Scheme 3.5). The anionic groups should be
immobile, and most of the Li+ will be available for carrying current. Below I
describe some previous studies of anion insertion via click chemistry and then
present studies aimed at determining whether the triazole or thioether linkers
alter Li+ conductivity.
114
Scheme 3.5. Proposed single-ion conductors prepared by synthesis of PEO
containing alkene or alkyne groups and subsequent attachment of anions to
these groups via click chemistry.
2.3.1. Prior Use of Click Chemistry for Creating Proton-Conducting
Membranes.
To the best of my knowledge, no studies reported using click chemistry to
prepare Li+ electrolytes. However, several groups employed click chemistry to
synthesize proton-conducting materials. Since proton and Li+ conduction are
similar, in the following section I first review the used of click chemistry
(alkyne-azide7 or thiol-ene
8) for post-functionalization of polymers to create
proton-conductive membranes.
115
O O SO
ONN
N
O
NaO3S
n
OOSO
ON
NN
O
NaO3S
NN
N
NNN
n
Scheme 3.6. Polysulfone structures synthesized by Bielawski’s et al for
proton-conduction.9
Especially relevant to this work, Bielawski et al. synthesized
polysulfone-based polyanions for proton-conductive membranes in methanol
fuel cells.9 Scheme 3.6 shows the structure of these polymers, in which
azide-containing polysulfone was partially functionalized with sulfonate side
chains via alkyne-azide click chemistry; the rest of the azide groups served as
crosslinking points to prepare a gel-like material. The performance of fuel cells
containing click-functionalized polysulfone membranes was comparable to that
116
with cells containing Nafion-based membranes, with a maximum power output
of 130 mW/cm.2
Scheme 3.7. Polyacrylate structures prepared by Martwiset et al. for formation
of membranes that exhibit proton conductivity at 200 oC.
10
Martwiset et al. synthesized polyacrylates containing different numbers of
1H-1,2,3-triazole groups (Scheme 3.7).10
They did not use click chemistry for
post-functionalization of the polymers, but the 1H-1,2,3-triazole groups served
as proton donors (Scheme 3.7) in proton-conducting membrane. In an
anhydrous environment at 200 oC, such membranes exhibited a maximum
conductivity of 17.5 µS/cm, which is comparable to the conductivity of Nafion
under these conditions.
117
Scheme 3.8. Poly(ether ether ketone) prepared by Gao et al for reaction with
3-mercaptopropyltrimethoxysilane via click chemistry.11
Gao et al. used thiol-ene chemistry to attach the mercaptopropyl
trimethoxysilane to a poly(ether ether ketone) derivative (Scheme 3.8).11
Subsequent crosslinking catalyzed by hydrochloric acid gave a polymer/silica
hybrid material with high dimensional and oxidative stabilities. Although the
proton conductivity of this material is lower than that of the original sulfonated
poly(ether ether ketone), presumably due to cross-linking, the material
maintained relatively high conductivity (10-2
S/cm at room temperature), 5%
and 10% weight loss temperature of the membrane are higher than 280 oC,
these properties made this series of membranes a good alternative for proton
exchange membranes in fuel cell application.
2.3.2. Synthesis of PEO-Containing Click Functionalities
Scheme 3.9. The thioether and triazole structures that result from (a) thiol-ene
and (b) alkyne-azido click chemistry, respectively.
The above examples of the use of click chemistry to prepare
118
proton-conductive polymer electrolyteS suggest that the resulting structures
(either thiol-ethers or 1,2,3-triazoles, Scheme 3.9) are not obstacles to proton
transport. However, I found no previous studies that employed click
chemistry to functionalize polymers for Li+ conduction.
(a)
(b)
Scheme 3.10. (a) Scheme of ideal lithium transport in an electrolyte material
and (b) scheme of lithium transport if the click functionality (triazole or thioether)
impedes Li+ transport.
Scheme 3.10 illustrates a possible challenge of the click structure to Li+
conductivity. The X-axis represents the lithium transport path, and the Y-axis
shows energy barriers for lithium transport. If the click structure has little or no
effect on lithium transport, lithium will encounter no additional barriers to
migration, as shown in Scheme 3.10 (a). The 1,2,3-triazole and sulfide
119
structures that result from click chemistry, could potentially associate with Li+
to decrease mobility. Click structures, particularly triazole, may make the
polymer back bone more rigid and give a high Tg that could reduce chain
mobility and decrease Li+ conductivity.
12 In these cases, high energy barrier
will appear across the whole lithium transport path, as shown in Scheme 3.10
(b). Finally, the solubility of Li+ in the polymer may decrease because of
unfavorable association with the click functionality.13 Before applying click
chemistry in this field, we decided to examine the influence of the click
structure on Li+ transport in PEO, and this required synthesis of PEO
containing triazoles and thioethers. Dipropargyl and diazido tetraethylene
glycol (Scheme 3.11a) will react to give triazole-containing PEO, and diallyl
and dithiol tetraethylene glycol (Scheme 3.11b) will form sulfur-containing
PEO, so we synthesized these reactants.
Scheme 3.11. (a) Monomers synthesized to prepare triazole-containing PEO,
(b) monomers to that will react to give sulfur-containing PEO.
120
TsCl/KOHr. t.
Scheme 3.12. Two methods for synthesis of dipropargyl tetraethylene glycol.
Reaction of propargyl bromide and tetraethylene glycol successfully gives
dipropargyl tetraethylene glycol in one step (Route 1, Scheme 3.12), but the
propargyl bromide starting material is relatively expensive ($58 for 50 g of an
80 wt% solution in toluene). More importantly this material is potentially
explosive and quite hazardous. To enable large scale synthesis while avoiding
use of the hazardous starting material, we developed Route 2 (Scheme 3.12),
which uses ditosyl tetraethylene glycol as an intermediate and reaction with
propargyl alcohol. We synthesized the target molecule using Route 2 at a
similar yield to Route 1, around 60%.
The tosylate derivative is a very useful and convenient intermediate to
covert hydroxyl groups to other functionalities.14
Conversion of the hydroxyl
group to tosylate using tosyl chloride is quantitative for many substrates, the
reaction condition is mild, and extraction purification usually gives pure product.
In fact, we synthesized three of the four compounds for click reactions using
the tosylate intermediate (Scheme 3.13). The only drawback to this method is
that tosyl chloride is toxic.
121
Scheme 3.13. Synthesis of several step-growth polymerization monomers via
the ditosyl derivative.
Scheme 3.14. Synthesis of diallyl tetraethylene glycol.
In principle, the method to synthesize dipropargyl tetraethylene glycol in
Scheme 3.13 could be further modified to obtain diallyl tetraethylene glycol.
However, allyl bromide is a relatively cheap commercial material ($35 for 250
mL, Aldrich) and is not hazardous, so we synthesized diallyl tetraethylene
glycol directly from tetraethylene glycol in the one step reaction shown in
Scheme 3.14.
122
Figure 3.6. Kinetics of step-growth polymerization between dipropargyl and
diazido tetraethylene glycol.
Scheme 3.15. Step-growth polymerization of diazido and dipropargyl
tetraethylene glycol.
Step-growth polymerization of diazido and dipropargyl tetraethylene
glycol (Scheme 3.15) was conducted using pre-synthesized Cu(PPh3)Br
catalyst. Figure 3.6 shows that after 4 h the reaction conversion plateaus
around 80%. Polymer was isolated by precipitation after adding the reaction
123
solution into ether, and GPC analysis of the polymer product gave Mw=8.1x104
and PDI=3.0.
Scheme 3.16. Step-growth polymerization of dithiol and diallyl tetraethylene
glycol.
Step-growth polymerization of dithio and diallyl tetraethylene glycol was
conducted via a thermally activated process (Scheme 3.16). GPC analysis of
the polymer product gave Mw=7,400 and PDI=1.1.
2.3.3. Comparison of the Conductivity of Li Salts in PEO and PEO with
Click Functionalities.
To determine if the triazole functionality affects the conductivity of Li salts in
PEO, we compared the conductivity of LiClO4 dissolved in a commercially
available polyethylene oxide (PEO, MV=105), with the conductivity of the
polymer obtained from polymerization of diazido and dipropargyl
tetraethylene glycol (Mw=8.1 x 104). Mv is calculated from the viscosity of a
polymer solution. Because polymer chains with higher molecular weights make
solutions much more viscous than chains with smaller molecular weights, Mv >
124
Mw, which is greater than Mn.
Figure 3.7. Conductivities of mixtures of LiClO4 with pure PEO (black squares)
and triazole-containing PEO (red circles) at different ratios of PEO to LiClO4.
The O/Li ratios in the mixture were determined from the masses of LiClO4 and
PEO added, and these ratios only include the O atoms from PEO.
Measurements occurred at 90 oC.
PEO with this large molecular weight is a solid with crystalline regions.
Previous studies show that the majority of current conduction occurs through
amorphous regions, so we determined conductivity with liquid polymers at 90
oC. The melting point of PEO is around 60 o
C. Figure 3.5 compares the
conductivity of electrolytes prepared with pure PEO and with PEO containing
triazole groups. In the pure PEO material (Mv=105), as the O/Li ratios
decreases from 128 to 64, conductivity increases due to more Li+ and ClO4
-
125
species in the mixture. The conductivity reaches a peak value of 0.039 S/cm.
Further increases in the LiClO4 concentration (O/Li ratios between 64 and 16)
do not increase conductivity. Previous work shows that at high salt
concentrations ions pair or aggregate, reducing the number and overall
mobility of the ions.15,16
Most importantly, electrolytes made with pure PEO
and PEO containing the triazole structure have similar conductivities. Thus, the
triazole groups that result from alkyne-azido click chemistry do not greatly
impede Li+ transport.
Figure 3.8. Conductivities of mixtures of LiClO4 with pure PEO (black squares)
and thioether-PEO (red circles) at different ratios of PEO to LiClO4. The O/Li
ratios in the mixture were determined from the masses of LiClO4 and PEO
added, and these ratios only include the O atoms from PEO. Measurement
occurred at 90 oC.
126
Figure 3.8 compares the conductivities of electrolytes made from pure PEO
and PEO containing thioether groups. A commercial poly(ethyleneoxide) (PEO)
with a molecular weight (Mw= 8,000) similar to that of the thioether PEO
served as the control polymer for these experiments. In this case, conductivity
generally increases with increasing concentrations of LiClO4 (decreasing O/Li
ratios). Comparison of Figures 3.7 and 3.8 suggests that the conductivities
are generally a factor of 2 or so higher in the lower molecular weight PEO
(Figure 3.6). The conductivities with pure PEO are about the same as in the
PEO prepared with thiol-ene click chemistry, suggesting that the thioethers do
not impede Li+ transport.
At a specific temperature, ionic conductivity is proportional to the number
of carriers, the charge of the carriers and their mobility. Both cations and
anions contribute to the ionic conductivity data measured by AC impedance
spectroscopy. Thus, the data in Figure 3.7 and 3.8 reflect the mobility of both
lithium cations and perchlorate anions. Previous studies show that with LiClO4
in PEO, 70% - 80% of the conductivity is due to perchlorate anions. It might be
possible that the triazole of thioether species disrupts conductivity from Li+ and
not from ClO4-, but since Li
+ contributes only 20% - 30% of the conductivity, we
do not detect it. However, given that the data show no evidence of a trend in
lower conductivity with triazole or thioethers, any effect would likely be small.
3. Conclusions
The conductivities of single-ion conductors based on nanoparticles with
127
grafted polyanions and nanoparticles with mono-layers of anions are similar,
despite the larger number of lithium counterions accompanying the polyanions.
This suggests that most of the lithium counterions in the polyanion-grafted
particles do not conduct current, probably due to the low solubility of
polyelectrolyte in PEO. However, electrolytes with polyanion-modified
nanoparticles show relatively large increases in conductivity as temperature
increases, suggesting that more Li+ may be available at high temperature due
to conformational changes.
To create single-ion conductors with higher conductivity, we are
considering grafting anions to PEO using click chemistry. This will avoid
problems with anion solubility in PEO. However, the triazole or thioether
groups in click linkers might impede conductivity. To examine this, we
polymerized tetraethylene oxides using click chemistry and determined the
conductivity of mixtures of LiClO4 with these polymers. Triazole and
thioether-containing PEO were synthesized with one triazole or thioether for
every tetraethylene oxide repeating unit. Conductivities were essentially the
same for LiClO4 mixed with pure PEO and with the new polymers, suggesting
that triazole and thioether groups do not impede Li+ transport.
4. Experimental Section
4.1. Materials
Sodium azide (500 g, Alfa Aesar, 99%), propargyl bromide (125 g, 80 wt%
solution in toluene, Aldrich), potassium carbonate (500 g, ACP Chemicals),
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p-toluenesulfonyl chloride (500 g, ACP Chemicals), thiourea (1 kg, Aldrich),
allyl bromide (1 L, reagent grade 97%, Aldrich), poly(ethyleneoxide) (250 g,
Mv=100,000, Aldrich), poly (ethyleneoxide) (500 g, Mn=8,000, Aldrich), sodium
hydride (100 g, 60% dispersion in mineral oil, Aldrich), tetraethylene glycol (1
kg, 99%, Aldrich), lithium perchlorate (100 g, ≥99%, Aldrich) and triethylene
glycol (1 kg, 99%, Aldrich) were used as received. Cu(I)Br (99.999%, Aldrich)
was purified using saturated aqueous NaBr solution. THF was distilled over
sodium metal and benzophenone.
4.2. Characterization
1H and
13C NMR spectra were collected using a Varian UnityPlus-500
spectrometer in CDCl3 with the residual proton signals from the solvent
serving as the chemical shift standard. Conductivity data were collected from
an HP 4192A LF Impedance Analyzer scanning from 5 Hz to 13 MHz with an
applied voltage of 10 mV. The sample cell contains two steel disks that serve
as symmetric electrodes separated by a Teflon collar containing electrolyte
with a radius of 0.61 cm and a thickness of 0.0175 cm. Electrolytes were
equilibrated at a pre-determined temperature for at least 10 minutes before
measurement. The molecular weights of polymers were determined by gel
permeation chromatography (GPC) using two PL-gel 20 m Mixed A columns
and a Waters R401 Differential Refractometer detector at room temperature.
THF served as the eluting solvent at a flow rate of 1 mL/min, and
mono-disperse polystyrene standards were used to calibrate the molecular
129
weights. The concentration of the polymer solutions used for GPC
measurements was 1 mg/mL. FT-IR spectra were collected in a Mattson
Galaxy 300 spectrometer. FT-IR samples were made by mixing with KBr,
grounded and pressed to pellets. Liquid materials were spread on a KBr pellet
and directly characterized in the instrument.
Quantitative Li analysis was performed using a Varian 710-ES ICP Optical
Emission Spectrometer. Six standard solutions (LiCl concentration of 0, 0.05,
0.5, 1, 2 and 4.5 ppm in 2 wt% HNO3) were used to prepare calibration curves.
Concentrations determined using emission at wavelengths of 460.289 nm,
670.783 nm, 610.365 nm were essentially the same
4.3. Synthesis
Synthesis of Tris (triphenylphosphine) copper(I) bromide Cu(PPh3)3Br: 6
g of triphenylphosphine (23 mmol) was dissolved in 100 mL boiling methanol in
a 250 mL flask. After addition of 1.43 g CuBr2 (10 mmol), the product formed
as a white precipitate, which was collected by filtration and dried under
vacuum at 90 oC overnight. The reaction gave 4.2 g product (62.3% yield )
with a melting point of 169 oC.
17
Synthesis of ditosyl tetraethylene glycol: Tetraethylene glycol (5.1 g, 0.05
mol) was dissolved in 60 mL of THF in a 250 mL round bottom flask. Twenty g
of tosyl chloride (0.105 mol) was added and the mixture was cooled in an ice
bath. In a separate Erlenmeyer flask, 25 g of KOH was dissolved in 30 mL of
deionized water. This KOH solution was transferred to an addition funnel and
130
slowly added into the 250 mL flask over 20 min. After the addition, the ice bath
was removed, and the reaction was allowed to proceed at room temperature
overnight. Most of THF was removed by rotary evaporation, and the product
was extracted from the residual solution with dichloromethane (3 x 100 mL).
The organic layer was washed with deionized water (4 x 200 mL) and dried
over MgSO4. The solvent was removed by rotary evaporation, and the product
was dried under vacuum to give 23.8 g of product as a viscous liquid (94%
yield). See Appendix 1 for the 1H NMR spectrum.
Synthesis of diazido tetraethylene glycol: Ditosyl tetraethylene glycol
(10.04 g, 0.02 mol), sodium azide (3.9 g, 0.06 mol) and 150 mL DMF were
mixed in a 500 mL flask at 90 oC overnight. After vacuum distillation to remove
DMF, the residual mixture was dissolved in 70 mL deionized water and the
product was extracted into dichloromethane (3 x 100 mL). The organic layer
was washed three times with 200 mL of deionized water and dried over
MgSO4. After rotary evaporation of solvent, the product was purified by silica
column chromatography (hexane/EtOAc=1:1), to give 3 g of product as a light
orange oil (61.5% yield). See Appendix 4 for the 1H NMR spectrum.
Synthesis of dipropargyl tetraethylene glycol:
Route 1 (using tetraethylene glycol and propargyl bromide): In a 250 mL
3-neck flask under N2, 5.68 g tetraethylene glycol (28.4 mmol) was dissolved
in 60 mL dry THF prior to gradual addition of 5.68 g sodium hydride (0.142 mol)
while stirring. After 20 minutes, the 3-neck flask was placed in an ice bath, and
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a solution containing 12.52 g of propargyl bromide (91 mmol) and 0.022 g
18-crown-6 (0.08 mmol) in 30 mL dry THF was slowly added to the flask
through an addition funnel over 10 minutes. The ice bath was then removed,
and the reaction was allowed to proceed at room temperature overnight.
Subsequently, 30 mL of deionized water was added, and the mixture was
stirred for 40 minutes to quench the reaction. Most of the THF was removed
by rotary evaporation, and the product was extracted from the residual solution
with dichloromethane (3 x 150 mL). The combined organic layer was dried
over MgSO4 and column chromatography (silica, hexane/ethyl acetate 1/4)
gave 3.3 g pure product (12.8 mmol, 45.2% yield).
Route 2 (using ditosyl tetraethylene glycol and propargyl alcohol): In a
300 mL beaker 7.5 g NaH in mineral oil (0.1875 mol) was added to 150 mL
pentane and stirred with a magnetic bar for 10 min. The NaH in the suspension
was allowed to settle, and a 50 mL syringe was used to carefully remove the
supernatant. The above process was repeated to give purified NaH. Next, 10.5
g propargyl alcohol (0.1875 mol) was dissolved in 200 mL dry THF in a 500 mL
round bottom flask, and 7.5 g of NaH was slowly transferred into this flask
under N2. After 30 min of stirring at room temperature, 20 g ditosyl
tetraethylene glycol was added, and the flask was heated at 60 oC overnight.
Fifty mL of deionized water was added to the flask, and after 10 min, most of
the THF was removed by rotary evaporation. The product was extracted in
dichloromethane (3 x 100 mL) and washed with deionized water (4 x 200 mL)
132
before drying over MgSO4. The solvent was removed by rotary evaporation,
and the product was purified by silica column chromatography
(hexane/EtOAc=1:1) to give 7 g of product (65% yield) as a light yellow oil. See
Appendix 7 for the 1H NMR spectrum.
Alkyn-azido Step growth polymerization: 1.318 g of diazido tetraethyleen
glycol (5.4 mmol), 1.458 g of diacetylene tetraethylene glycol (5.4 mmol) and
0.05 g Cu(PPh3)3Br (0.01 equiv.) were dissolved in 20 mL of chloroform in a
100 mL Schlenk flask and allowed to react at 60 oC for 24 h, After cooling to
room temperature, this solution was added dropwise to 200 mL diethyl ether
with strong stirring. Product was precipitated as a light brown viscous oil, which
was dissolved in chloroform and precipitated in ether again. The product was
dried under vacuum (1.2 g, 43% yield). GPC (THF solvent, PS standard)
showed Mn=2.73 x 104, Mw=8.11 x 10
4, PDI=3.0. See Appendix 15 for the
1H
NMR spectrum.
Synthesis of dithiol tetraethylene glycol: In a 250 mL round bottom flask,
20.1 g ditosyl tetraethylene glycol (0.04 mol), 40 mL of ethanol, and 6.1 g of
thiourea (0.08 mol) were added to 30 mL of deionized water. The solution was
purged with nitrogen for 15 minutes, and the flask was fitted with a condenser.
After reflux for 15 h, a solution of 4 g NaOH (0.1 mol) in 40 mL deionized water
was added, and after another 2 h of reflux, the flask was placed in an ice bath.
Fifteen mL of concentrated HCl solution was added to neutralize the solution,
and the product was then extracted in dichloromethane (3 x 50 mL). The
133
combined dichloromethane solution was dried over MgSO4, solvent was
removed by rotary evaporation, and vacuum distillation gave 4 g of dithiol
tetraethylene glycol (0.025 mol, 62%) as colorless oil. See Appendix 12 for the
1H NMR spectrum.
Synthesis of diallyl tetraethylene glycol: In a 500 mL round bottom flask,
11.6 g of dihydroxyl tetraethylene glycol (0.06 mol) and 14 g of powderized
KOH (0.25 mol) were dissolve in 200 mL of acetone. After placing the flask in
an ice bath, 10 mL of allyl bromide (0.12 mol) was slowly added over 10
minutes. The ice bath was then removed, and the mixture was allowed to react
at room temperature overnight. Acetone was removed using rotary
evaporation, and the product was dissolved in 300 mL dichloromethane.
Deionized water was used to wash the dichloromethane solution (3 x 80 mL),
the organic layer was dried using MgSO4, and solvent was removed by rotary
evaporation. Silica column chromatography (hexane/ethyl acetate 9/1) gave
10.84 g (0.042 mol, 70% yield) of product. See Appendix 10 for the 1H NMR
spectrum.
Thiol-ene Step growth polymerization: 6.46 g diallyl tetraethylene glycol
(0.024 mol), 5.36 g dithiol tetraethylene glycol (0.024 mol) were dissolved with
100 mL dichloromethane in a 250 mL round bottom flask. The solution was
purged with nitrogen for 30 minutes and was done in a 50 oC oil bath for 24 h.
To work up the reaction, the mixture was put under rotovac to remove residual
solvent. The product was dissolved in 100 mL chloroform and added dropwise
134
to 200 mL diethyl ether with strong stirring. Product was obtained as a light
yellow viscous oil, which was dissolved in chloroform and precipitated in ether
again. Polymer product was dried under vacuum as viscous oil (11.5 g, 97.3%).
GPC: Mn=6,700, Mw=7,400, PDI=1.1. See Appendix 14 for the 1H NMR
spectrum.
135
APPENDIX B
136
Appendix B1. 1H NMR spectrum of ditosyl tetraethyleneglycol in CDCl3.
137
Appendix B2. 13
C NMR spectrum of ditosyl tetraethyleneglycol in CDCl3.
138
Appendix B3. FT-IR spectrum of ditosyl tetraethyleneglycol.
139
Appendix B4. 1H NMR spectrum of diazido tetraethyleneglycol in CDCl3.
140
Appendix B5. 13
C NMR spectrum of diazido tetraethyleneglycol in CDCl3.
141
Appendix B6. FT-IR spectrum of diazido tetraethyleneglycol.
142
Appendix B7. 1H NMR spectrum of dipropargyl tetraethyleneglycol in CDCl3.
143
Appendix B8. 13
C NMR spectrum of dipropargyl tetraethyleneglycol in CDCl3.
144
Appendix B9. FT-IR spectrum of dipropargyl tetraethyleneglycol.
145
Appendix B10. 1H NMR spectrum of diallyl tetraethyleneglycol in CDCl3.
146
Appendix B11. FT-IR spectrum of diallyl tetraethyleneglycol.
147
Appendix B12. 1H NMR spectrum of dithiol tetraethyleneglycol in CDCl3.
148
Appendix B13. 13
C NMR spectrum of dithiol tetraethyleneglycol in CDCl3.
149
Appendix B14. 1H NMR spectrum of dithiol tetraethyleneglycol in CDCl3.
150
Appendix B15. FT-IR spectrum of dithiol tetraethyleneglycol.
151
Appendix B16. FT-IR spectrum of thioether-PEO.
152
Appendix B17. 1H NMR spectrum of triazole-PEO in CDCl3.
153
Appendix B18. FT-IR spectrum of triazole-PEO.
154
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155
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