New method for silica embedding on a PES membrane surface via in situ sol gel process and immobilization in a polyamide thin film composite

被引:12
作者
Berbar, Yassine [1 ,2 ]
Amara, Mourad [1 ]
Ammi-Said, Abdallah [1 ,2 ]
Yuan, Shushan [2 ]
Van der Bruggen, Bart [2 ]
机构
[1] USTHB, Fac Chem, Lab Hydromet & Mol Inorgan Chem, BP 32, Algiers 16111, Algeria
[2] Katholieke Univ Leuven, Dept Chem Engn, Celestijnenlaan 200F, B-3001 Heverlee, Belgium
关键词
Polyethersulfone nanofiltration membrane; Membrane surface modification; Silica thin film composite; In situ silica embedding; HEAVY-METAL IONS; NANOFILTRATION MEMBRANE; POLYETHERSULFONE MEMBRANES; INTERFACIAL POLYMERIZATION; SIO2; NANOPARTICLES; HYBRID MEMBRANES; WATER DESALINATION; REVERSE-OSMOSIS; FUEL-CELL; PERFORMANCE;
D O I
10.1016/j.jece.2017.07.008
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A novel method to incorporate silica on a polyethersulfone (PES) membrane surface was successfully developed. An in situ hydrolysis/condensation of tetraethylorthosilicate (TEOS) precursor was carried out, followed by coating as thin film composite (TFC) via interfacial polymerization. PES membranes casted from 20 and 23 wt.% PES in N-methyl-pyrrolidone (NMP) solutions were prepared by phase inversion. The membrane surfaces were modified by TEOS silica precursors, dispersed in ethanol at different concentrations (0.1, 0.3 and 0.5 w/v%) and catalyzed by a NH3/H2O mixture. Immobilization of the prepared silica on the membrane surface was obtained by adding a polyamide coating. The modified membranes were characterized by FTIR, SEM, AFM, and TGA, which confirmed the successful embedding of silica particles by the in situ sol gel process. In the best conditions, rejection of MgSO4 and Na2SO4 reached 85 and 94.2% respectively. This was consolidated by a proportionally high water flux of 62.2 and 64.15 L m(-2) h(-1) for MgSO4 and Na2SO4 salt solutions, respectively, at an operational pressure of 5 bar.
引用
收藏
页码:3604 / 3615
页数:12
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