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颗粒间静电双层相互作用对胶体悬浮液错流膜过滤中渗透通量下降的影响:一项实验研究

Effect of Interparticle Electrostatic Double Layer Interactions on Permeate Flux Decline in Crossflow Membrane Filtration of Colloidal Suspensions: An Experimental Investigation.

作者信息

Faibish RS, Elimelech M, Cohen Y

机构信息

School of Engineering and Applied Science, University of California, Los Angeles, California, 90095

出版信息

J Colloid Interface Sci. 1998 Aug 1;204(1):77-86. doi: 10.1006/jcis.1998.5563.

Abstract

A systematic study on the effect of electrostatic double layer interaction on permeate flux decline and deposit cake formation in crossflow membrane filtration of colloidal suspensions is reported. Three monodisperse silica suspensions with diameters of 47, 110, and 310 nm were used as model colloids, and a tubular zirconia membrane with an average pore diameter of 20 nm was used as a model membrane. The magnitude and range of the electrostatic double layer interactions were controlled via changes in solution ionic strength and pH. The coupling between colloidal interactions and hydrodynamic forces was investigated by changing the transmembrane pressure and particle size. The results indicate that the rate of flux decline is strongly dependent on solution ionic strength and, to a much lesser degree, on solution pH (for the investigated pH range 6.1-10.0). Variations in flux decline rate with solution ionic strength are especially significant as the particle size decreases. Particle cake thickness, permeability, and porosity generally increased with a decrease in solution ionic strength for a given particle size. For given physical and chemical conditions, the cake layer porosity increased with decreasing particle size, while cake permeability decreased with decreasing particle size. These trends are consistent with the increased importance of double layer repulsive forces in controlling the cake layer structure as the solution ionic strength and particle size decrease. Pressure relaxation experiments indicated that the particle cake layer is reversible, implying no irreversible deposition (attachment) of silica colloids onto the zirconia membrane surface. Copyright 1998 Academic Press.

摘要

本文报道了关于静电双层相互作用对胶体悬浮液错流膜过滤中渗透通量下降和沉积滤饼形成影响的系统研究。使用了三种直径分别为47、110和310 nm的单分散二氧化硅悬浮液作为模型胶体,并使用平均孔径为20 nm的管状氧化锆膜作为模型膜。通过改变溶液离子强度和pH值来控制静电双层相互作用的大小和范围。通过改变跨膜压力和颗粒尺寸来研究胶体相互作用与流体动力之间的耦合。结果表明,通量下降速率强烈依赖于溶液离子强度,而在较小程度上依赖于溶液pH值(在所研究的pH范围6.1 - 10.0内)。随着颗粒尺寸减小,通量下降速率随溶液离子强度的变化尤为显著。对于给定的颗粒尺寸,颗粒滤饼厚度、渗透率和孔隙率通常随着溶液离子强度的降低而增加。在给定的物理和化学条件下,滤饼层孔隙率随着颗粒尺寸减小而增加,而滤饼渗透率随着颗粒尺寸减小而降低。这些趋势与随着溶液离子强度和颗粒尺寸减小,双层排斥力在控制滤饼层结构中的重要性增加是一致的。压力松弛实验表明颗粒滤饼层是可逆的,这意味着二氧化硅胶体不会不可逆地沉积(附着)在氧化锆膜表面。版权所有1998年学术出版社。

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