Interlayer adsorption of cationic dye on cationic surfactant-modified and unmodified montmorillonite

被引:59
|
作者
Zhang L.-L. [1 ]
Zaoui A. [1 ]
Sekkal W. [1 ]
Zheng Y.-Y. [1 ,2 ,3 ]
机构
[1] Univ. Lille, IMT Nord Europe, JUNIA, Univ. Artois, ULR 4515 - LGCgE, Laboratoire de Génie Civil et géo-Environnement, Lille
[2] School of Civil Engineering, Sun Yat-Sen University, Guangzhou
[3] China & Southern Marine Science and Engineering Guangdong Laboratory (Zhuhai), Zhuhai
关键词
Adsorption; Cationic dye; Molecular dynamics; Organoclay;
D O I
10.1016/j.jhazmat.2022.130107
中图分类号
学科分类号
摘要
Water pollution by toxic organic dyes is one of the most critical health and environmental problems worldwide. By means of molecular dynamics method, the present work aims to evaluate the applicability of montmorillonite (Mt) modified by hexadecyltrimethylammonium cations (HDTMA+) compared to unmodified Na-Mt for the adsorption of cationic methylene blue (MB) dye. The results showed that the adsorption energy of MB on both HDTMA-Mt and Na-Mt absorbent ranged from − 100 to − 250 kJ/mol, indicating the effectiveness of two types of adsorbents in dye water treatment. The highest adsorption energy was found at w = 50% in each adsorbent system. Adsorption mechanisms of MB depend on molecular orientations, which is influenced by the surfactant and water content. The adsorption mechanism of MB is chemisorption dominated by strong electrostatic interaction between CH3 groups of MB and oxygen atoms of Mt surfaces. Besides, physisorption also plays a minor role in MB orientations. It is found that the existence of cationic surfactants can slightly improve the adsorption capacity of MB only at higher water content through enlarging the interlayer space of Mt and reducing mobility of MB. However, there will be a negative impact on the reduction of adsorption sites for dyes especially at low water content. Our results provide a possible application for swelling clay minerals being a promising adsorbent for dyes-surfactants co-existing wastewater treatment. © 2022 Elsevier B.V.
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