Understanding organic solvent permeation during nanofiltration via electrical impedance spectroscopy (EIS)
To better understand organic solvent nanofiltration mechanisms, Electrical Impedance Spectroscopy was used to analyze real-time changes in the membrane, which functions as a variable dielectric and exhibits changes in capacitance as the solvent permeates. The 350 kDa membranes were composed of polyd...
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sg-ntu-dr.10356-1800052024-09-09T07:10:54Z Understanding organic solvent permeation during nanofiltration via electrical impedance spectroscopy (EIS) Ng, Angie Qi Qi Tanudjaja, Henry Jonathan Yeo, Ming Ming Chew, Jia Wei School of Chemical and Biomedical Engineering Nanyang Environment and Water Research Institute Singapore Membrane Technology Centre Engineering Organic solvent filtration Membrane-solvent interactions To better understand organic solvent nanofiltration mechanisms, Electrical Impedance Spectroscopy was used to analyze real-time changes in the membrane, which functions as a variable dielectric and exhibits changes in capacitance as the solvent permeates. The 350 kDa membranes were composed of polydimethylsiloxane active layers atop polyacrylonitrile supports, while the two solvents were ethanol and isopropyl alcohol (IPA). Four key differences between the solvents are revealed. Firstly, the flux decline was greater for ethanol because the higher polarity promoted adsorption. Secondly, during filtration, the conductance decreased for ethanol but increased for IPA. Thirdly, increasing pressure increased the membrane thickness for ethanol but not for IPA. Fourthly, the permeation mechanisms vary between the two solvents at different pressures. At the lower initial flux, flux decrease was due to extensive adsorption for ethanol, but to the accumulation of IPA impeding permeation for IPA. For the higher initial flux, the gentler flux decline for ethanol was due to greater membrane swelling, whereas the steeper decline for IPA was due to the high driving force promoting permeation through the DP layer to the membrane substrate. The results here underscore the importance of membrane-solvent interactions in affecting OSN performance. Agency for Science, Technology and Research (A*STAR) Ministry of Education (MOE) Published version We acknowledge funding from the A*STAR (Singapore) Advanced Manufacturing and Engineering (AME) under its Pharma Innovation Programme Singapore (PIPS) program (A20B3a0070), A*STAR (Singapore) Advanced Manufacturing and Engineering (AME) under its Individual Research Grant (IRG) program (A2083c0049), the Singapore Ministry of Education Academic Research Fund Tier 1 Grant (2019-T1- 002-065; RG100/19) and the Singapore Ministry of Education Academic Research Fund Tier 2 Grant (MOE-MOET2EP10120-0001). 2024-09-09T07:10:53Z 2024-09-09T07:10:53Z 2024 Journal Article Ng, A. Q. Q., Tanudjaja, H. J., Yeo, M. M. & Chew, J. W. (2024). Understanding organic solvent permeation during nanofiltration via electrical impedance spectroscopy (EIS). Journal of Industrial and Engineering Chemistry, 136, 603-614. https://dx.doi.org/10.1016/j.jiec.2024.02.049 1226-086X https://hdl.handle.net/10356/180005 10.1016/j.jiec.2024.02.049 2-s2.0-85186684042 136 603 614 en A20B3a0070 A2083C0049 2019-T1-002-065 RG100/19 MOE-MOET2EP10120-0001 Journal of Industrial and Engineering Chemistry © 2024 The Author(s). Published by Elsevier B.V. on behalf of The Korean Society of Industrial and Engineering Chemistry. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). application/pdf |
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Engineering Organic solvent filtration Membrane-solvent interactions Ng, Angie Qi Qi Tanudjaja, Henry Jonathan Yeo, Ming Ming Chew, Jia Wei Understanding organic solvent permeation during nanofiltration via electrical impedance spectroscopy (EIS) |
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To better understand organic solvent nanofiltration mechanisms, Electrical Impedance Spectroscopy was used to analyze real-time changes in the membrane, which functions as a variable dielectric and exhibits changes in capacitance as the solvent permeates. The 350 kDa membranes were composed of polydimethylsiloxane active layers atop polyacrylonitrile supports, while the two solvents were ethanol and isopropyl alcohol (IPA). Four key differences between the solvents are revealed. Firstly, the flux decline was greater for ethanol because the higher polarity promoted adsorption. Secondly, during filtration, the conductance decreased for ethanol but increased for IPA. Thirdly, increasing pressure increased the membrane thickness for ethanol but not for IPA. Fourthly, the permeation mechanisms vary between the two solvents at different pressures. At the lower initial flux, flux decrease was due to extensive adsorption for ethanol, but to the accumulation of IPA impeding permeation for IPA. For the higher initial flux, the gentler flux decline for ethanol was due to greater membrane swelling, whereas the steeper decline for IPA was due to the high driving force promoting permeation through the DP layer to the membrane substrate. The results here underscore the importance of membrane-solvent interactions in affecting OSN performance. |
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School of Chemical and Biomedical Engineering |
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School of Chemical and Biomedical Engineering Ng, Angie Qi Qi Tanudjaja, Henry Jonathan Yeo, Ming Ming Chew, Jia Wei |
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Article |
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Ng, Angie Qi Qi Tanudjaja, Henry Jonathan Yeo, Ming Ming Chew, Jia Wei |
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Ng, Angie Qi Qi |
title |
Understanding organic solvent permeation during nanofiltration via electrical impedance spectroscopy (EIS) |
title_short |
Understanding organic solvent permeation during nanofiltration via electrical impedance spectroscopy (EIS) |
title_full |
Understanding organic solvent permeation during nanofiltration via electrical impedance spectroscopy (EIS) |
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Understanding organic solvent permeation during nanofiltration via electrical impedance spectroscopy (EIS) |
title_full_unstemmed |
Understanding organic solvent permeation during nanofiltration via electrical impedance spectroscopy (EIS) |
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understanding organic solvent permeation during nanofiltration via electrical impedance spectroscopy (eis) |
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2024 |
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https://hdl.handle.net/10356/180005 |
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1814047206364151808 |