Surfactant-modified montmorillonite by benzyloctadecyldimethylammonium chloride for removal of perchlorate

被引:41
|
作者
Luo, Wuhui [1 ]
Sasaki, Keiko [1 ]
Hirajima, Tsuyoshi [1 ]
机构
[1] Kyushu Univ, Dept Earth Resources Engn, Fukuoka 8190395, Japan
关键词
Montmorillonite; Benzyloctadecyldimethylammonium chloride; Perchlorate removal; Configuration; Hydrophobic interaction; pi-pi interaction; CLAY-MINERALS; ORGANO-MONTMORILLONITES; AQUEOUS-SOLUTIONS; ACTIVATED CARBON; DRINKING-WATER; ADSORPTION; CETYLTRIMETHYLAMMONIUM; SPECTROSCOPY; SILICATES; MOLECULES;
D O I
10.1016/j.colsurfa.2015.06.025
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A high adsorption capacity (0.90 mmol/g) of perchlorate was achieved on organo-montmorillonites (organo-MMTs) through modification by benzyloctadecyldimethylammonium chloride (BODMA-Cl), which typically possesses a long alkyl chain and a benzene ring. With increase in the amount of BODMA-Cl added, the XRD and FTIR results showed that the BODMA(+)/BODMA-Cl achieved a lateral bilayer, pseudo-trilayer and tilted paraffin-like bilayer configurations in the MMT interlayer space with improvement of ordered arrangement, and the formation of bilayers and/or micelles on the external surface also was demonstrated by TG-DTA and zeta potential curves. The EDX spectra of resultant products and adsorption isotherms of perchlorate on organo-MMTs suggested that a larger content of BODMA-Cl resulted in synthesized adsorbent with a greater adsorption capacity, because neutral BODMA-Cl is predominantly responsible for ion exchange with perchlorate. The maximum adsorption capacity was attained not only by enhanced affinity between BODMA(+) and metallic layer of MMT, but also by increasing density of intercalated BODMA-Cl which is caused by hydrophobic interactions through long alkyl chains and pi-pi interactions through benzene rings among BODMA+/BODMA-Cl. It was also emphasized that the high adsorption capacity of perchlorate on organo-MMTs was achieved with a rapid adsorption rate and stably maintained against variations in temperature, initial solution pH and co-existing competitive anion. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:616 / 625
页数:10
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