fos could be used for aoc determination
DESCRIPTION
FOS could be used for AOC determination. 3 mg L -1. 1 mg L -1. Schaule, G., Moschnitschka, D., Schulte, S., Tamachkiarow, A., Flemming, H.-C. (2007): Biofilm growth in response to various concentrations of biodegradable material in drinking water. Wat. Sci. Technol. 55, 191-195. - PowerPoint PPT PresentationTRANSCRIPT
FOS COULD BE USED FOR AOC DETERMINATION
0
0,5
1
1,5
2
2,5
0 24 48 72 96 120 144 168
Time [h]
sens
or s
igna
l [V]
tota
l cel
l num
ber [
cells
/cm
²]
sensor 2 week 1sensor 1 week 2sensor 2 week 2sensor 1 week 3sensor 2 week 3Sensor 1 week 4Sensor 2 week 4Sensor 1 week 5Sensor 2 week 5total cell number week 1total cell number week 2total cell number week 3total cell number week 4total cell number week 5
100
105
104
103
102
101
106
107
DOC concentration week 1-3 ca. 1 mg/LDOC concentration week 4-5 ca. 3 mg/L
3 mg L-1
1 mg L-1
Biofilm Centre
Schaule, G., Moschnitschka, D., Schulte, S., Tamachkiarow, A., Flemming, H.-C. (2007): Biofilm growth in response to various concentrations of biodegradable material in drinking water. Wat. Sci. Technol. 55, 191-195
Principle
LEVEL 1: COMMERCIAL HEAT TRANSFER MEASUREMENT DEVICE „NEOSENS FS“
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Neosens FS-900/FS-1000 sensor (Neosens S.A., Labege, France)
NEOSENS FS-900/FS-1000 DETAILS (1)
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Sensor head with tip
Example: Application in cooling water systemNEOSENS FS-900/FS-1000 DETAILS (2)
Biofilm Centre
5Biofilm Centre
f is related to the mass of the attached film
D is related to the viscoelasticity
Level 1: Quartz crystal microbalance (LOT)
QMB: MASS CHANGES, THICKNESS, DENSITY, VISCOSITY AND SHEAR MODULUS DETECTABLE
Surface materialAuTiO2SiO2Polystyrene
t
MassThicknessDensityViscosityShear modulus
Real Time measurement
*Application dependant
MassThicknessDensityViscosityShear modulus
Sample size, ~1 nm – ~5* μm
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THE DEVICE9
Quartz crystal, volume above sensor ~ 40 l
Flow channels for temperature stabilisation, volume ~ 100 l
Cross section of flow moduleBiofilm Centre
Level 1:Mechatronic Surface Sensor (MSS)
Actuator(Piezo)
Sensor(Accelerometer)
The MSS concept is based on the effect of mass on the vibration of a material The material in the systerm is used (PVC, PE, steel, iron etc.)
The piezo element is composed of a metal sheet between two piezo layers that has a bending movement when a low electric voltage (< 1 V) is applied
The accelerometer includes a small chip that measures extremely small vibrations
L. Melo & A. Pereira, Univ. of Porto
Biofilm Centre
Computer
Actuator
Sensor
The software makes the actuator vibrate at a well defined amplitude and frequency
The surface vibration is detected by the sensor
The software acquires the wave detected by the sensor, determines its amplitude and performs the ‘amplitude normalization’
Acquisition process in MSS
L. Melo & A. Pereira, Univ. of Porto L. Melo & A. Pereira, Univ. of Porto
Response to initial cell attachment
Amplitude of the output signal is inversely proportional to the biofilm cells number
Good correlation obtained
Pseudomonas fluorescensTurbulent flow
L. Melo & A. Pereira, Univ. of Porto
Biofilm Centre
MSS configuration
Southampton UniversityFront view Back viewL. Melo & A. Pereira, Univ. of Porto
Biofilm Centre
Level I Scattered light (FOS)„Detection of a deposit Differential turbidity (DTM) on a surface“ Pressure drop
Heat transfer resistanceWeight increaseVelocity of soundPhotoacoustic spectroscopyPiezo-electrical device (PD)
Level II FTIR-ATR-spectroscopy (FTIR-ATR)„Biological aspects of deposit“ Fluorescence spectroscopy sensor (FluS)Level III FTIR-ATR-spectroscopy (FTIR-ATR)„Detailed information“ Raman spectroscopy
X-ray photoelectron spectroscopy
Levels of information of some monitoring principles:
Biofilm Centre
Flemming, H.C. (2003): Role and levels of real time monitoring for successful anti-fouling strategies. Wat. Sci. Technol. 47 (5), 1-8
Biofilm monitoring by fluorescent biomolecules
Substance Excitation EmissionTyrosin 257 nm 303 nm
Tryptophane 287 nm 348 nm
Serine 295 nm 330 nm
Phenylalanine 260 nm 282 nm
NADH/NADPH 340 nm 460 nm
ATP 272 nm 380 nm
Chlorophyll 340 nm 460 nm
Some fluorescent biomolecules
Approach: Use autofluorescence of biomolecules as signature for biomass
FLUORESCENCE ANALYSIS OF BACKSCATTERED LIGHT
OptiQuad sensor Detection of biomolecules
by their fluorescence
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• Fluorescence 1 excitation 290 nm, emission detection 340 nm tryptophan (biofilm)
• Fluorescence 2 excitation 340 nm, emission detection 460 nm NADH (bacteria)
• Dispersion 290 nm, 340 nm and 810 nm surface deposit characteristics
• Refraction 663 nm particles in deposit• Transmission 290 nm, 340 nm, 663 nm
and 810 nm deposit amount & nature
CONFIGURATION AFTER PRELIMINARY STUDIES WITH DRINKING WATER BIOFILM ON QUARTZ COUPONS:
Biofilm Centre
Level I Scattered light (FOS)„Detection of a deposit Differential turbidity (DTM) on a surface“ Pressure drop
Heat transfer resistanceWeight increaseVelocity of soundPhotoacoustic spectroscopyPiezo-electrical device (PD)
Level II FTIR-ATR-spectroscopy (FTIR-ATR)„Biological aspects of deposit“ Fluorescence spectroscopy sensor (FluS)Level III FTIR-ATR-spectroscopy (FTIR-ATR)„Detailed information“ Raman spectroscopy
X-ray photoelectron spectroscopy
Levels of information of some monitoring principles:
Biofilm Centre
Flemming, H.C. (2003): Role and levels of real time monitoring for successful anti-fouling strategies. Wat. Sci. Technol. 47 (5), 1-8
LEVEL 3: INFRARED FLOW-THROUGH CELL Detailed chemical information about deposit Biological material: amide I and II bands Bypass device
Water
Biofilm
Light source
Detector
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Disassembled flow-cell
Internal reflectance elements (IRE)
ZnSe Ge
Mounted flow-cell
Biofilm generated on crystal
Evanescent wave IR source
Detector
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1 2 3 4 5
spectral windows
[AU]
wavenumbers cm-1
cell wall fatty acids
proteins
polysaccharides
fingerprint region (fine differences between strains)
proteins + polysaccharides
SIMPLIFIED INTERPRETATION OF THE BACTERIAL IR SPECTRUM
-OH (various polymers)
Biofilm Centre
A:\Bioflm3.001 biofilm gel 90/99 16.04.1999 film 16/ 4/1999
100015002000250030003500Wavenumber cm-1
0.05
0.10
0.15
0.20
Abs
orba
nce
Uni
ts
IR SPECTRUM OF A PROCESS WATER BIOFILM
Unusually high content of polysaccharides compared to washed bacteria (due to EPS)
Biofilm Centre
CONCLUSIONS
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Nutrients are potential biomass AOC determination indicates fouling potential, new methods are available – e.g., using bioluminescence, flow cytometry Detection of biofouling: on surfaces Required: „Eyes in the system“
on-line, real time, non-destructively, in-situ, representative automatic
Early warning of biofouling, timely and effective countermeasures Verification of efficacy - breaking out of viscious cycle Some commercial devices available, need application improvement! Not yet fully met in membranes – use periphery for reference Information: indirect, by physical parameters Detailed information possible but still in laboratory phase The List:
Optical sensors (FOS) Heat transfer resistance (LOT) Mechanical sensors (QMB, MSS) Advanced sensors (SpectroQuad, FTIR)
22Biofilm Centre
23Biofilm Centre
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24Biofilm Centre
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