Sustaining fouling resistant membranes: Membrane fabrication, characterization and mechanism understanding of demulsification and fouling-resistance

生物污染 结垢 化学工程 膜污染 聚丙烯腈 超亲水性 微滤 材料科学 粘附 化学 复合材料 聚合物 接触角 生物化学 工程类
作者
Bing He,Yajie Ding,Jianqiang Wang,Zhikan Yao,Weihua Qing,Yingjie Zhang,Fu Liu,Chuyang Y. Tang
出处
期刊:Journal of Membrane Science [Elsevier BV]
卷期号:581: 105-113 被引量:73
标识
DOI:10.1016/j.memsci.2019.03.045
摘要

Antifouling performance of membranes is the key obstacle limiting their practical applications for oil/water separation. In this study, a sustaining antifouling membrane was fabricated by constructing polydopamine (PDA) micro-/nano-spheres on a polyacrylonitrile (PAN) nanofibrous membrane. The secondary PDA nano-spheres not only strengthened the bonding of primary micro-spheres with the substrate, but also diversified the hierarchical structure and chemistry. The composite showed enhanced superhydrophilicity and underwater superoleophobicity. Permeability of PAN-PDAc membrane was maintained as high as 11666 ± 978 Lm−2h−1bar−1 with separation efficiency of higher than 99.9% over a 2-h continuous filtration. This permeability was about 2.7 times of pristine PAN membrane (4260 ± 430 Lm−2h−1bar−1). The extrusion and cutting demulsification on the confined space of PAN-PDA surface was proposed. Antifouling mechanism of the superhydrophilic membrane was first theoretically elucidated based on hydration ability and adhesion free energy with recourse to thermal analysis and Derjaguin-Landau-Verwey-Overbeek theory respectively. It was found that PDA micro-/nano-spheres mediated membrane showed strong hydration ability (higher fraction of non-freezable water) and weak adhesion towards toluene (low free energy of adhesion) compared to pristine PAN membrane. These findings would lead to a better understanding of antifouling demulsification mechanism and improved design of sustaining antifouling membranes for oil/water separation.
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