2017
DOI: 10.1016/j.memsci.2017.06.089
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Superoleophobic surface modification for robust membrane distillation performance

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Cited by 131 publications
(102 citation statements)
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“…Even though protonated amine-functional groups were also detected on the 6h-mPVDF membrane surface, there were fewer of these groups as compared with the PDA/PEI membrane surface. This was corroborated with the chemical structures of the respective deposited layers [56,191,196]. As such, the electrostatic repulsion between the negatively charged SDS unimers and the negatively charged 6h-mPVDF membrane surface was more dominant than the electrostatic attraction between these unimers and the protonated amine-functional groups.…”
Section: Underwater Oil-membrane Interactionssupporting
confidence: 66%
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“…Even though protonated amine-functional groups were also detected on the 6h-mPVDF membrane surface, there were fewer of these groups as compared with the PDA/PEI membrane surface. This was corroborated with the chemical structures of the respective deposited layers [56,191,196]. As such, the electrostatic repulsion between the negatively charged SDS unimers and the negatively charged 6h-mPVDF membrane surface was more dominant than the electrostatic attraction between these unimers and the protonated amine-functional groups.…”
Section: Underwater Oil-membrane Interactionssupporting
confidence: 66%
“…The absorption peak observed at 1701 cm -1 on the mPVDF membranes is indicative of carbonyl/carboxyl groups, suggesting the successful deposition of carboxyl-functional groups during the accelerated oxidative process induced by SP under slightly acidic conditions [191,196]. This in turn rendered the mPVDF membrane surface more hydrophilic than the previously reported PDA/PEI coated membrane [56]. Fig.…”
Section: Characterizations Of Membrane Surface Chemistrymentioning
confidence: 72%
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