Tailoring the micro-structure of PVC/SMA-g-PEG blend ultrafiltration membrane with simultaneously enhanced hydrophilicity and toughness by in situ reaction-controlled phase inversion

被引:28
作者
Chen, Rui [1 ,2 ]
Mao, Liuyong [1 ,2 ]
Matindi, Christine N. [1 ,2 ]
Liu, Gansheng [1 ,2 ]
He, Jintao [1 ,2 ]
Cui, Zhenyu [1 ,2 ]
Ma, Xiaohua [1 ,2 ]
Fang, Kuanjun [3 ]
Wu, Biao [4 ]
Mamba, Bhekie B. [5 ]
Li, Jianxin [1 ,2 ,5 ]
机构
[1] Tiangong Univ, Natl Ctr Int Joint Res Membrane Sci & Technol, State Key Lab Separat Membranes & Membrane Proc, Tianjin 300387, Peoples R China
[2] Tiangong Univ, Sch Mat Sci & Engn, Tianjin 300387, Peoples R China
[3] Collaborat Innovat Ctr Ecotext Shandong Prov, 308 Ningxia Rd, Qingdao 266071, Peoples R China
[4] Tianjin Tisun ITACSA Technol CO LTD, Xuefu Ind Pk, Tianjin 300382, Peoples R China
[5] Univ South Africa, Inst Nanotechnol & Water Sustainabil, Coll Sci Engn & Technol, Sci Campus, ZA-1710 Johannesburg, South Africa
关键词
Polyvinyl chloride; Styrene-maleic anhydride; Polyethylene glycol; Esterification; Reaction-controlled non-solvent induced phase; inversion; NANOFILTRATION MEMBRANES; ANTIFOULING PERFORMANCE; WATER-TREATMENT; IMPROVEMENT; FABRICATION; NANOPARTICLES; PERMEABILITY; SELECTIVITY; ANHYDRIDE); PERMEATION;
D O I
10.1016/j.memsci.2022.120545
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
An in-situ reaction controlled non-solvent induced phase separation (RC-NIPS) method was developed to tailor the morphology of polyvinyl chloride (PVC)/styrene-maleic anhydride (SMA) grafting polyethylene glycol (PEG) (SMA-g-PEG) blend ultrafiltration (UF) membrane. Herein, PVC and SMA was dissolved in dimethylacetamide (DMAc) solvent to prepare a casting solution (16 wt% polymer concentration) at 50 degrees C. Subsequently, PEG (20 kDa) as an additive and reactant was added to the casting solution at a mass ratio of PEG to the polymer 1/1 wt/ wt. to enhance the hydrophilicity and mechanical elongation of the membrane. Results demonstrated that the casting solution with PVC/SMA = 3/1 wt/wt. was an entirely compatible system. The viscosity of the casting solution with adding PEG gradually increased from 692 mPa s to 1880 mPa s at the initial stage and 4780 mPa s at 42 h, then rose sharply to 27,320 mPa s at 84 h. This behavior was ascribed to the esterification reaction between PEG and SMA, leading to pre-gelation and gelation of the system. Whereafter, SMA-g-PEG graft polymers were obtained. Meanwhile, the degree of grafting (DG) increased from 0.40% at 12 h of the reaction to 2.61% at 42 h. Afterwards, a phase inversion using water as coagulation was used to prepare PVC/SMA-g-PEG blend membrane after a certain time of the esterification reaction. It was found that the morphology of resultant membranes systematically changed from asymmetric structure with a dense top layer and finger-like sublayer at the initial stage to a dense layer with a fully sponge-like structure after 18-42 h reaction. The PVC/SMA-g-PEG membrane obtained after the reaction of 42 h demonstrated better hydrophilicity, high pure water permeance and excellent toughness due to the internal plasticization of water molecules. The membrane also exhibited a high BSA rejection (>95%) and fouling recovery rate (FRR) (85.9%). Our work provides some insights on tailoring the UF membrane structure and simultaneously enhancing permeability, antifouling performance and toughness.
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页数:13
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