首页> 美国卫生研究院文献>Membranes >Modification of Polysulfone Ultrafiltration Membranes via Addition of Anionic Polyelectrolyte Based on Acrylamide and Sodium Acrylate to the Coagulation Bath to Improve Antifouling Performance in Water Treatment
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Modification of Polysulfone Ultrafiltration Membranes via Addition of Anionic Polyelectrolyte Based on Acrylamide and Sodium Acrylate to the Coagulation Bath to Improve Antifouling Performance in Water Treatment

机译:基于丙烯酰胺和丙烯酸钠的阴离子聚电解质加入聚砜超滤膜的改性凝血浴提高水处理中的防污性能

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摘要

Surface modification of polysulfone ultrafiltration membranes was performed via addition of an anionic polymer flocculant based on acrylamide and sodium acrylate (PASA) to the coagulation bath upon membrane preparation by non-solvent induced phase separation (NIPS). The effect of PASA concentration in the coagulant at different coagulation bath temperatures on membrane formation time, membrane structure, surface roughness, hydrophilic-hydrophobic balance of the skin layer, surface charge, as well as separation and antifouling performance was studied. Scanning electron microscopy (SEM), atomic force microscopy (AFM), Fourier transform infrared (FTIR) spectroscopy, contact angle and zeta potential measurements were utilized for membrane characterization. Membrane barrier and antifouling properties were evaluated in ultrafiltration of model solutions containing human serum albumin and humic acids as well as with real surface water. PASA addition was found to affect the kinetics of phase separation leading to delayed demixing mechanism of phase separation due to the substantial increase of coagulant viscosity, which is proved by a large increase of membrane formation time. Denser and thicker skin layer is formed and formation of macrovoids in membrane matrix is suppressed. FTIR analysis confirms the immobilization of PASA macromolecules into the membrane skin layer, which yields improvement of hydrophilicity and change of zeta potential. Modified membrane demonstrated better separation and antifouling performance in the ultrafiltration of humic acid solution and surface water compared to the reference membrane.
机译:通过加入基于丙烯酰胺和丙烯酸钠(PASA)的阴离子聚合物絮凝剂通过非溶剂诱导的相分离(NIPS)在凝结浴中加入基于丙烯酰胺和丙烯酸钠(丙烯酸钠)来进行聚砜超滤膜的表面改性。研究了PASA浓度在凝结剂在不同凝血浴温度下的膜形成时间,膜结构,表面粗糙度,皮肤层,表面电荷的亲水 - 疏水性平衡,以及分离和防污性能的影响。扫描电子显微镜(SEM),原子力显微镜(AFM),傅里叶变换红外(FTIR)光谱,接触角和Zeta电位测量用于膜特征。在含有人血清白蛋白和腐殖酸的模型溶液以及真实地面水中的模型溶液中评价膜屏障和防污性能。发现PASA加法以影响相分离的动力学,导致相分离的延迟脱晶机制由于凝结剂粘度的大幅增加,这通过大增加膜形成时间来证明。形成密度和较厚的皮肤层,并抑制膜基质中的宏体的形成。 FTIR分析证实了PASA大分子的固定到膜皮层中,从而产生了改善亲水性和Zeta电位的变化。改性膜与参考膜相比,在腐殖酸溶液和表面水的超滤中显示出更好的分离和防污性能。

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