Mechanisms controlling adsorption of natural organic matter on surfactant-modified iron oxide-coated sand

被引:43
作者
Ding, Chunli [1 ]
Shang, Chii [1 ]
机构
[1] Hong Kong Univ Sci & Technol, Dept Civil & Environm Engn, Kowloon, Hong Kong, Peoples R China
关键词
Chemical force microscopy; Hydrophobic interaction; Ligand exchange; Quaternary ammonium; Surface interaction; HUMIC SUBSTANCES; FORCE MICROSCOPY; MODIFIED ZEOLITE; SORPTION; REMOVAL; WATER; ACID; DESORPTION; CHROMATE;
D O I
10.1016/j.watres.2010.04.014
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Mechanisms contributing to the adsorption of natural organic matter (NOM) on surfactant-modified iron oxide-coated sand (LOGS) were explored by microscopic surface characterization techniques and adsorption tests. Electrostatic interactions that were thought to be from the positively charged, surface-coated surfactant, hexadecyltrimethyl ammonium (HDTMA), seemed to be unimportant, likely because the outward-pointing tail groups of the surface-coated HDTMA monolayers hindered the interactions. Improved hydrophobic interactions followed by ligand exchange are believed to be the dominant mechanisms. Atomic force microscopy (AFM) force analysis with chemically modified tips was used to explore the adsorption mechanisms between NOM and IOCS, where an iron oxide-coated mica surface was utilized as a substitute for the IOCS surface. It demonstrates the changes of pull-on forces and the increases in hydrophobic interactions from the modification of IOCS with HDTMA. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3651 / 3658
页数:8
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