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Microwave/ultrasound-assisted modification of montmorillonite by conventional and gemini alkyl quaternary ammonium salts for adsorption of chromate and phenol: Structure-function relationship

机译:常规/双子烷基季铵盐微波/超声波辅助改性蒙脱土吸附铬酸盐和苯酚的结构-功能关系

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Butane-1,4-bis(dodecyl dimethyl ammonium bromide) (gBDDA) and dodecyl trimethyl ammonium bromide (DTMA) in same stoichiometric amounts were applied to modify montmorillonite (Mt) under microwave and ultrasound conditions. The composition and structure of products were obtained through multiple characterizations including XRD, FTIR, TG/DTG, SEM, TEM, and N-2 adsorption/desorption measurements, and the adsorption performance of chromate and phenol on these products were also investigated. Intercalations of gBDDA and DTMA into interlayer space of Mt were observed, but the amount of anchored modifier on the external surface was larger for gBDDA compared with DTMA when the stoichiometric amount of modifier larger than 1.0 times cation exchange capacity of Mt was added. Although there was no significant difference in morphology among products, the interlayer space distance, specific surface area, and pore size distribution were closely associated with the species and amount of applied modifier. Adsorption of phenol on products through partition mechanism relied on not only organic content, but also the configuration of modifier. Meanwhile, adsorption of chromate mainly depended on the presence of counter ion (bromide), which accounted for the high adsorption capacity and initial adsorption rate on gOMt-0.75. The fitting parameters of adsorption results using pseudo-second order model and Freundlich model suggested that gBDDA-modified Mt could sequester phenol or chromate in the faster manner with higher affinity. Compared with the conventional surfactant such as DTMA, the study revealed that, using gemini surfactant such as gBDDA to modify Mt would significantly reduce or even has the potential to eradicate the secondary pollution by modifier release during adsorption process. This study provides a new direction for Mt modification intended to be used as adsorbents to treat polluted water with high standards such as drinking water. (C) 2018 Elsevier B.V. All rights reserved.
机译:在微波和超声条件下,将化学计量相同的1,4-双(十二烷基二甲基二甲基溴化铵)(gBDDA)和十二烷基三甲基溴化铵(DTMA)用于改性蒙脱土(Mt)。通过XRD,FTIR,TG / DTG,SEM,TEM和N-2吸附/脱附等多种表征,获得了产物的组成和结构,并研究了铬酸盐和苯酚在这些产物上的吸附性能。观察到gBDDA和DTMA插入到Mt的层间空间中,但是当添加的化学计量比大于Mt阳离子交换容量的1.0倍时,与DTMA相比,gBDDA的外表面锚定改性剂的量更大。尽管产品之间的形态没有显着差异,但是层间距离,比表面积和孔径分布与改性剂的种类和用量密切相关。通过分配机理在产品上吸附苯酚不仅依赖于有机物含量,还依赖于改性剂的构型。同时,铬酸盐的吸附主要取决于抗衡离子(溴化物)的存在,这说明在gOMt-0.75上高的吸附容量和初始吸附速率。拟二阶模型和Freundlich模型对吸附结果的拟合参数表明,gBDDA修饰的Mt可以更快地螯合苯酚或铬酸盐,具有更高的亲和力。与传统的表面活性剂(如DTMA)相比,研究表明,使用双子表面活性剂(如gBDDA)来修饰Mt会显着降低甚至具有消除吸附过程中改性剂释放造成二次污染的潜力。这项研究为Mt改性提供了新的方向,旨在用作吸附剂来处理高标准的饮用水(如饮用水)。 (C)2018 Elsevier B.V.保留所有权利。

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