Adsorption of Cu2+ and methylene blue on dodecyl sulfobetaine surfactant-modified montmorillonite

被引:74
作者
Fan, Hongwei [1 ]
Zhou, Limei [1 ]
Jiang, Xiaohui [1 ]
Huang, Qiang [1 ]
Lang, Wencheng [1 ]
机构
[1] China West Normal Univ, Chem Synth & Pollut Control Key Lab Sichuan Prov, Nanchong 637002, Sichuan, Peoples R China
关键词
Montmorillonite; Surfactant; Methylene blue; Cu2+; Adsorption; TEXTILE WASTE-WATER; AQUEOUS-SOLUTION; HEAVY-METALS; CATIONIC DYE; HUMIC-ACID; REMOVAL; IONS; KAOLINITE; MECHANISMS; COMPOSITE;
D O I
10.1016/j.clay.2014.04.001
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
The dodecyl sulfobetaine surfactant-modified montmorillonite (Mt-SB12) was synthesized using montmorillonite (Mt) and dodecyl sulfobetaine surfactant. The as-prepared material was used as adsorbent for removal of Cu2+ and methylene blue (MB) in single and binary systems. In the single systems, the results showed that the kinetics of adsorption followed the linear pseudo-second-kinetic model. The results of interlayer diffusion indicated that MB had higher diffusion rate than Cu2+. For the Mt-SB12, the isotherm results showed that MB adsorption followed the Langmuir and Cu2+ adsorption followed the Freundlich isotherm. The adsorption capacities for Cu2+ and MB at 298 K and pH 5 were (10.2 and 254.0) mg/g, respectively. For the Mt, Cu2+ and MB adsorptions both followed the Langmuir. The adsorption capacities for Cu2+ and MB at 298 K and pH 5 were (9.5 and 1502) mg/g, respectively. So the dodecyl sulfobetaine surfactant-modified Mt is more beneficial to adsorb MB than Mt. Dubinin-Radushkevitch (D-R) equation indicated Cu2+ and MB adsorptions were chemical ion exchange adsorption and adsorption thermodynamics showed they were spontaneous and endothermic processes. In binary systems, Cu2+ and MB showed competitive adsorption. The adsorption capacity of Cu2+ or MB would be decreased with the increased concentration of another adsorbate. Mt-SB12 exhibited relative higher affinity and selectivity to MB. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:150 / 158
页数:9
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