Yao Shu-Di, Gao Xin-Yu, Guo Ben-Hua, Bao Nan, Xie Hui-Jun, Liang Shuang
School of Environmental Science and Engineering, Shandong University, Ji'nan 250100, China.
Huan Jing Ke Xue. 2012 Jun;33(6):1884-90.
Interfacial interactions involved in reverse osmosis (RO) membrane fouling by humic acid were quantitatively evaluated using the XDLVO (extended Derjaguin-Landau-Verwey-Overbeek) approach. The role of each individual interfacial interaction during membrane fouling was elucidated with special emphasis devoted into the influence of Ca2+ under different solution pHs. The results showed that, regardless of the presence of Ca2+, van der Waals interaction favoring fouling contributed the most to the interfacial interactions at pH 3, whereas the polar interaction inhibiting fouling played a dominant role at pH 7 and pH 10. Electrostatic double layer interaction appeared to be the weakest in all cases, thus contributing the least to membrane fouling. It was the changing of polar interaction that gave rise to the influence of Ca2+ on membrane fouling, which turned out to be more significant at lower pH. Ca2+ would accelerate humic acid RO membrane fouling at most cases. Correlation analysis between interfacial free energy and fouling extent revealed that XDLVO approach could reasonably predict humic acid RO membrane fouling behaviors under different solution conditions.
采用XDLVO(扩展的Derjaguin-Landau-Verwey-Overbeek)方法对腐殖酸导致的反渗透(RO)膜污染过程中的界面相互作用进行了定量评估。阐明了膜污染过程中各界面相互作用的作用,特别强调了不同溶液pH值下Ca2+的影响。结果表明,无论Ca2+是否存在,在pH为3时,有利于污染的范德华相互作用对界面相互作用的贡献最大,而在pH为7和pH为10时,抑制污染的极性相互作用起主导作用。在所有情况下,静电双层相互作用似乎最弱,因此对膜污染的贡献最小。正是极性相互作用的变化导致了Ca2+对膜污染的影响,在较低pH值下这种影响更为显著。在大多数情况下,Ca2+会加速腐殖酸对RO膜的污染。界面自由能与污染程度之间的相关性分析表明,XDLVO方法能够合理预测不同溶液条件下腐殖酸RO膜的污染行为。