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Professor: Cheng-Ho ChenGraduate: Po-Huei Tseng
Date: 101.12.19
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OutlineIntroductionExperimentResults and DiscussionConclusionsReferences
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Introduction(1)
Ionomers: macromolecules composed of a small but significant proportion of constitutional units (less than 10%) containing an ionic and/or ionizable group.
The ionic groups cause a micro-phase separation of the ionic moieties (ionic aggregation) within the non-ionic matrix and act as physical crosslinks.
Ionomers of low glass-transition non-crystalline polymers can be used as ionic thermoplastic elastomers (TPEs) if the ionic aggregates are sufficiently weakened at the processing temperatures.
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Introduction(2)TPEs: melt-processable polymers composed of a
continuous elastomeric phase.Both the precursor elPP-g-MA and the ionomers were
synthesized by melt-processing.
The neutralization reaction was monitored by infrared spectroscopy and a method is proposed to determine the effective neutralization degree (ND).
Various forms of sodium hydroxide and sodium acetate were used to compare their efficiency of elPP-g-MA neutralization.
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OutlineIntroductionExperimentResults and DiscussionConclusionsReferences
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MaterialsMaterials Purchase Purity Company
Isotactic homopolymer PP powder Moplen HF500N Basell
2,5-bis(tert-butyl-peroxy)-2,5dimethylhexane[DHBP]
Luperox 101XLS50
50 wt% blend with Si
Arkema
Maleic anhydride(MA) 99% Acros
N-bromosuccinimide(NBS) 99% Acros
Sodium Acetate Trihydrate(NaAcTH)
99% Aldrich
NaOH(pellets) 99+% Aldrich
NaOH(powder) 97% Aldrich
Sodium Acetate Anhydrous(SAA) 99% Aldrich
Tolune(analytical grade) Fisher6
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Equipments
Equipments Model Manufacturer
DSC DSC 821e Mettler Toledo
SEC GPCV 2000 Waters Alliance
FTIR Nexus 670 Nicolet
TGA TGA/SDTA 851e Mettler Toledo
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Synthesis 1 elPP-g-MA
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Synthesis 2 Ionomer
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Characterization
Quantification of the grafted speciesDifferential scanning calorimetry (DSC)Size exclusion chromatography(SEC)Fourier transform infrared (FTIR)
spectroscopyThermogravimetric analysis (TGA)Rheological properties
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Quantification of the grafted species
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DSC
Crystallinity and Tg of elPP-g-MA and ionomers: evaluated from a second heating ramp from -50 to 220℃ at 10℃/min.
The device was calibrated with indium and zinc.
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SEC
The mobile phase: 1,2,4-trichlorobenzene(TCB)
The concentration of the sample:
2 mg/mL in TCB
dissolution: shaking at 160℃ for 1 h
The injection volume: 215 μLTemperature: held constant at 145℃
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FTIR
the peak height of the 973 cm-1 absorption band to an absorbance of 1
The frequency range of absorption bands area:1.carbonyl of the anhydride (1750-1830 cm-1)2.carbonyl of the carboxylic acid (1650-1750
cm-1)
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TGA
heating rate: 10℃/min under air atmosphere(100 mL/min)
temperature: 25-600℃
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Rheological properties
Equipment: Rubber Process Analyser RPA 2000, Alpha
Technologies
Frequency sweep tests: performed at 120℃ at a strain rate of 10% over an angular
frequency ranging from 300 to 1 rad/s
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OutlineIntroductionExperimentResults and DiscussionConclusionsReferences
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elPP-g-MA Characterization
The degradation of the molar mass is caused by a side reaction, β-scission, occurring during the functionalization. The crystallinity of elPP-g-MA is strongly reduced with respect to the starting PP, due to the epimerization reaction occurring in the presence of peroxide and NBS.
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Ionomer ND determination(1)
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Ionomer ND determination(2)
1863
1790
15701715
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Ionomer ND determination(3)
If the ND were calculated on the basis of the decrease of the anhydride band at 1790 cm-1 from elPP-g-MA (AanhelPP-g-MA) to ionomer (Aanhionomer), it would be overestimated due to the carboxylic acid functions contribution.
100ND MAgelPP
ionomer
anh
anh
A
A
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Ionomer ND determination(4)
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Influence of the nature of the base on ND
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NaOH 2.5 M > NaOH sol. NaAc*3H≒ 2O sol. > NaAc 2.5 M > NaAc. anh. sol.
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Ionomer CharacterizationDSCTGARheology
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DSCelPP-g-MA: Tg is around -4.2 and a weak ℃
broad melting peak.
Ionomers: only Tg
Tg for all the ionomers are similar to the one of elPP-g-MA.
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TGA
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Rheology
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ConclusionsThe choice of the base has a strong influence on the
neutralization degree.
As the neutralization yield never reaches 100%, the excess of the added sodium hydroxide may lead to corrosion.
Sodium acetate is preferred over sodium hydroxide.
The thermal stability in air atmosphere, shear storage modulus and complex viscosity in the flow region were largely increased as a function of the neutralization degree.
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References[1] Hess M, Jones RG, Kahovec J, Kitayama T, Kratochvíl P, Kubisa P, et al.
Terminology of polymers containing ionizable or ionic groups and of polymers containing ions (IUPAC recommendations 2006). Pure and Applied Chemistry 2006; 78(11); 2067-74.
[2] Holliday L, editor. Ionic polymers. London: Applied Science Publishers; 1975.
[3] Eisenberg A, editor. Ions in polymers. Washington, DC: American Chemical Society; 1980.
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[5] Schlick S, editor. Ionomers: characterisation, theory and applications. Boca Raton, Florida: CRC Press; 1996.
[6] Tant MR, Mauritz K, Wilkes G, editors. Ionomers: synthesis, structure, properties and applications. London: Springer; 1997.
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[8] Bagrodia S, Wilkes GL, Kennedy JP. New polyisobutylene-based model elastomeric ionomers: rheological behavior. Polymer Engineering and Science 1986; 26(10): 662-72.29
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[9] van der Mee MAJ, Abee RMA, Portale G, Goossens JGP, van Duin M. Synthesis, structure, and properties of ionic thermoplastic elastomers based on maleated ethylene/propylene copolymers. Macromolecules 2008;41(14): 5493-501.
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[13] molecular weight maleated ethylene-propylene copolymers (man-g-epm) as investigated by small-angle x-ray scattering. Macromolecules 2002; 35(1): 208-16.
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[15] Grady BP, Goossens JGP, Wouters MEL. Morphology of zinc-neutralized maleated ethylene-propylene copolymer ionomers: structure of ionic aggregates as studied by x-ray absorption spectroscopy. Macromolecules 2004; 37(23): 8585-91.
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[17] Henry G, Drooghaag X, Rousseaux D, Sclavons M, Devaux J, Marchand-Brynaert J et al., A practical way of grafting maleic anhydride onto polypropylene providing high anhydride contents without sacrificing excessive molar mass. Journal of Applied Polymer Sciences; Part A; Polymer Chemistry 2008; 46(9); 2936-47.
[18] Sclavons M, Franquinet P, Carlier V, Verfaillie G, Fallais I, Legras R, et al. Quantification of the maleic anhydride grafted onto polypropylene by chemical and viscosimetric titrations, and FTIR spectroscopy. Polymer 2000; 41: 1989-99.
[19] Burfield D, Loi P. The use of infrared spectroscopy for determination of polypropylene stereoregularity. Journal of Applied Polymer Science 1988;36(2): 279-93.
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