Characterization of anion-cationic surfactants modified montmorillonite and its application for the removal of methyl orange

被引:194
作者
Chen, Daimei [1 ]
Chen, Jian [2 ]
Luan, Xinlong [2 ]
Ji, Haipeng [2 ]
Xia, Zhiguo [1 ]
机构
[1] China Univ Geosci, Natl Lab Mineral Mat, Beijing 100083, Peoples R China
[2] China Univ Geosci, Sch Mat Sci & Technol, Beijing 100083, Peoples R China
关键词
Montmorillonite; Modification; Adsorption; Surfactant; Clay; AQUEOUS-SOLUTION; SORPTION BEHAVIOR; ORGANIC-COMPOUNDS; WASTE-WATER; ADSORPTION; KINETICS; DECOLORIZATION; BENTONITE; SURFACES; SMECTITE;
D O I
10.1016/j.cej.2011.05.013
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Anion-cationic, anionic and cationic surfactants modified montmorillonite (MMT) are prepared by incorporating cationic surfactants cetyl trimethyl ammonium bromide (CTMAB), anionic surfactants sodium stearate (SSTA) and their mixture to montmorillonite. The modified samples are characterized by X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy and Thermogravimetry-differential thermal analysis (TG-DTA). XRD result shows that both the anionic and cationic surfactants can be intercalated into the MMT, making the interlayer spaces of MMT expand. TG-DTA studies indicate the organic carbon contents of anion-cationic surfactants modified MMT are higher than the montmorillonite modified by anionic or cationic surfactants solely. The adsorption experiments indicate that CTMAB/10SSTA-MMT had the largest adsorption capacity compared with CTMAB-MMT and 10SSTA-MMT due to the formation of a highly effective partition medium by anion-cationic surfactant micelle. The adsorption kinetic of methyl orange onto the modified MMT samples can be best described by the pseudo-second-order model, and the adsorption isotherm is in good agreement with the Langmuir equation. The activation energy, change of free energy, enthalpy and entropy of anion-cationic modified MMT are also evaluated for the adsorption of methyl orange. Thermodynamic results indicate that the adsorption is a spontaneous and exothermic process. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:1150 / 1158
页数:9
相关论文
共 29 条
[1]   Characterization and determination of the thermodynamic and kinetic properties of p-CP adsorption onto organophilic bentonite from aqueous solution [J].
Akçay, M .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2004, 280 (02) :299-304
[2]   SORPTION CHARACTERISTICS OF ORGANIC-COMPOUNDS ON HEXADECYLTRIMETHYLAMMONIUM-SMECTITE [J].
BOYD, SA ;
MORTLAND, MM ;
CHIOU, CT .
SOIL SCIENCE SOCIETY OF AMERICA JOURNAL, 1988, 52 (03) :652-657
[3]   Mechanisms for the adsorption of substituted nitrobenzenes by smectite clays [J].
Boyd, SA ;
Sheng, GY ;
Teppen, BJ ;
Johnston, CJ .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2001, 35 (21) :4227-4234
[4]  
CASON R, 1977, Proceedings of the Oklahoma Academy of Science, V57, P116
[5]   Nanofiltration of textile plant effluent for color removal and reduction in COD [J].
Chakraborty, S ;
Purkait, MK ;
DasGupta, S ;
De, S ;
Basu, JK .
SEPARATION AND PURIFICATION TECHNOLOGY, 2003, 31 (02) :141-151
[6]   Sorption of p-nitrophenol by anion-cation modified palygorskite [J].
Chang, Yue ;
Lv, Xueqian ;
Zha, Fei ;
Wang, Yonggang ;
Lei, Ziqiang .
JOURNAL OF HAZARDOUS MATERIALS, 2009, 168 (2-3) :826-831
[7]   Preparation and characterization of anion-cation surfactants modified montmorillonite [J].
Chen, D. ;
Zhu, J. X. ;
Yuan, P. ;
Yang, S. J. ;
Chen, T. -H. ;
He, H. P. .
JOURNAL OF THERMAL ANALYSIS AND CALORIMETRY, 2008, 94 (03) :841-848
[8]   Adsorption of Methylene Blue from Aqueous Solution by Anionic Surfactant Modified Montmorillonite [J].
Chen, Daimei ;
Chen, Jian ;
Weng, Xuming ;
Luan, Xinlong ;
Ji, Haipeng ;
Xu, Feng .
ADVANCE IN ECOLOGICAL ENVIRONMENT FUNCTIONAL MATERIALS AND ION INDUSTRY II, 2011, 178 :29-+
[9]  
Freundlich H, 1906, Z PHYS CHEM-STOCH VE, V57, P385
[10]   PORE- AND SOLID-DIFFUSION KINETICS IN FIXED-BED ADSORPTION UNDER CONSTANT-PATTERN CONDITIONS [J].
HALL, KR ;
EAGLETON, LC ;
ACRIVOS, A ;
VERMEULEN, T .
INDUSTRIAL & ENGINEERING CHEMISTRY FUNDAMENTALS, 1966, 5 (02) :212-+