4.7 Article

A comparison of effect mechanisms of chlorination and ozonation on the interfacial forces of protein at membrane surfaces and the implications for membrane fouling control

期刊

JOURNAL OF MEMBRANE SCIENCE
卷 628, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.memsci.2021.119266

关键词

Pre-chlorination; Pre-ozonation; Interfacial forces; Protein-like foulants; Membrane fouling

资金

  1. National Natural Science Foundation of China [52070150]
  2. Research Grants Council of the Hong Kong Government [17210219, T21-711/16R]
  3. Science and Technology Innovative Team Plan of Shaanxi Province [2017KCT-19-01]
  4. Shaanxi Innovation and Guidance Special Project [2018HJCG-18, 2018SJRG-X-02]

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The research discovered that pre-chlorination and pre-ozonation have different effects on membrane fouling behavior, with variations in the interaction forces between BSA molecules at the membrane surface. Chlorination breaks the disulfide bonds between BSA molecules, while ozonation promotes their formation, resulting in different protein deposition behaviors on the membrane surface and corresponding fouling layer structures.
Pre-chlorination and pre-ozonation are the two most common pre-oxidation processes for fouling control of ultrafiltration membranes. However, few studies have explored and compared their effect mechanisms on membrane fouling behavior at the interfacial forces level. Accordingly, bull serum albumin (BSA) was used, and the changes in the interaction forces of BSA at the membrane surface after pre-chlorination and pre-ozonation were investigated. The results were combined with macro/micro analyses to unravel the effect mechanisms of chlorination and ozonation on membrane fouling behavior. Results demonstrated that the changes in the hydrophobic forces, hydrogen bonds and electrostatic repulsive forces between the membrane and BSA and between BSA molecules after pre-chlorination and pre-ozonation, were beneficial for membrane fouling control in theory, but not helpful. These changes in the non-covalent bonds appear to be completely masked by changes in disulfide bonds. The chlorination could break the disulfide bonds between BSA molecules, while ozonation could promote their formation. As a result, the deposition behavior of BSA onto the membrane surface and the structures of corresponding fouling layers after pre-chlorination were quite different from those after preozonation. Finally, two different membrane fouling behaviors were observed that membrane fouling was definitively mitigated by pre-chlorination but enhanced by pre-ozonation.

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