The role of electrostatic interactions on the rejection of organic solutes in aqueous solutions with nanofiltration

被引:213
作者
Verliefde, A. R. D. [1 ]
Cornelissen, E. R. [2 ]
Heijman, S. G. J. [1 ,2 ]
Verberk, J. Q. J. C. [1 ]
Amy, G. L. [3 ]
Van der Bruggen, B. [4 ]
van Dijk, J. C. [1 ]
机构
[1] Delft Univ Technol, Fac Civil Engn & Geosci, Dept Sanit Engn, NL-2600 GA Delft, Netherlands
[2] Kiwa Water Res, NL-3430 BB Nieuwegein, Netherlands
[3] UNESCO IHE, NL-2601 DA Delft, Netherlands
[4] Katholieke Univ Leuven, Dept Chem Engn, Lab Appl Phys Chem & Environm Technol, B-3001 Louvain, Belgium
关键词
rejection; NF/RO; charge interactions; organic acids; pharmaceuticals;
D O I
10.1016/j.memsci.2008.05.022
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The effects of electrostatic interactions on the rejection of organic solutes with nanofiltration membranes were investigated. For two different membranes, the rejection of selected organic acids, positively and negatively charged pharmaceuticals and neutral pharmaceuticals was investigated at different feed water chemistries (different ionic strengths and pH conditions, with and without the presence of NOM and divalent cations). It was concluded that for negatively charged membranes, electrostatic repulsion leads to an increase of the rejection of negatively charged solutes and electrostatic attraction leads to a decrease of the rejection of positively charged solutes, compared to neutral solutes. Neutral and positively charged solutes engage in hydrophobic interactions with negatively charged membranes, whereas negatively charged solutes do not engage in hydrophobic interactions since they cannot approach the membrane surface. This provides proof for the theory of an increased concentration of positively charged organic solutes and a decreased concentration of negatively charged organic solutes at the membrane surface compared to the bulk fluid. This concept may be denoted as "charge concentration polarisation". The concept was further used as a modelling tool to predict the effects of electrostatic interactions on the rejection of trace organic solutes. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:52 / 66
页数:15
相关论文
共 44 条
[1]   Atrazine and simazine removal mechanisms by nanofiltration: Influence of natural organic matter concentration [J].
Agbekodo, KM ;
Legube, B ;
Dard, S .
WATER RESEARCH, 1996, 30 (11) :2535-2542
[2]   Factors affecting the rejection of organic solutes during NF/RO treatment - a literature review [J].
Bellona, C ;
Drewes, JE ;
Xu, P ;
Amy, G .
WATER RESEARCH, 2004, 38 (12) :2795-2809
[3]   The role of membrane surface charge and solute physico-chemical properties in the rejection of organic acids by NF membranes [J].
Bellona, C ;
Drewes, JE .
JOURNAL OF MEMBRANE SCIENCE, 2005, 249 (1-2) :227-234
[4]   Removal of pesticides and other micropollutants by nanofiltration [J].
Berg, P ;
Hagmeyer, G ;
Gimbel, R .
DESALINATION, 1997, 113 (2-3) :205-208
[5]   Effects of organic and inorganic matter on pesticide rejection by nanofiltration [J].
Boussahel, R ;
Montiel, A ;
Baudu, M .
DESALINATION, 2002, 145 (1-3) :109-114
[6]   Influence of hydrophobicity on retention in nanofiltration of aqueous solutions containing organic compounds [J].
Braeken, L ;
Ramaekers, R ;
Zhang, Y ;
Maes, G ;
Van der Bruggen, B ;
Vandecasteele, C .
JOURNAL OF MEMBRANE SCIENCE, 2005, 252 (1-2) :195-203
[7]   Dichloroaniline retention by nanofiltration membranes [J].
Causserand, C ;
Aimar, P ;
Cravedi, JP ;
Singlande, E .
WATER RESEARCH, 2005, 39 (08) :1594-1600
[8]   Influences of molecular weight, molecular size, flux, and recovery for aromatic pesticide removal by nanofiltration membranes [J].
Chen, SS ;
Taylor, JS ;
Mulford, LA ;
Norris, CD .
DESALINATION, 2004, 160 (02) :103-111
[9]   Relating nanofiltration membrane performance to membrane charge (electrokinetic) characteristics [J].
Childress, AE ;
Elimelech, M .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2000, 34 (17) :3710-3716
[10]   Effects of natural organic matter and the raw water matrix on the rejection of atrazine by pressure-driven membranes [J].
Devitt, EC ;
Ducellier, F ;
Cote, P ;
Wiesner, MR .
WATER RESEARCH, 1998, 32 (09) :2563-2568