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CTMAB对BS-12修饰膨润土的复配修饰模式
引用本文:余 璐,孟昭福,李文斌,任 爽,吴 琼,刘 伟,白 丹.CTMAB对BS-12修饰膨润土的复配修饰模式[J].土壤学报,2016,53(2):543-551.
作者姓名:余 璐  孟昭福  李文斌  任 爽  吴 琼  刘 伟  白 丹
作者单位:1. 西北农林科技大学资源环境学院,陕西杨凌,712100;2. 西北农林科技大学资源环境学院,陕西杨凌 712100; 农业部西北植物营养与农业环境重点实验室,陕西杨凌 712100
基金项目:国家自然科学基金项目(41271244)和陕西省社会发展攻关项目(2013K13-01-05)共同资助
摘    要:研究了十六烷基三甲基溴化铵(CTMA)在十二烷基二甲基甜菜碱(BS-12)修饰膨润土表面的复配模式,通过BS-12膨润土表面Ca2+/2和CTMA总浓度(SCC)变化及20℃和40℃条件下CTMA吸附量的变化可知:存在离子交换和疏水键合模式。CTMA在25%、50%、100%BS-12修饰(25BS、50BS和100BS)膨润土表面出现疏水键的临界比例(RC)分别为20.30%、11.56%和2.00%,且疏水比例随CTMA复配比例(R)及其摩尔分数的增大而增大,疏水键合模式占绝对优势的临界比例(RC′)分别为200%、150%和100%。对于BS-12单一修饰及BS-12+CTMA复配修饰比例之和,50%及200%分别是膨润土表面出现疏水键合及其占绝对优势的转折点。RRC,离子交换模式;RC≤R≤RC′,离子交换与疏水键合共存;RRC′,疏水键合占绝对优势。RC、RC′及CTMA最大吸附量(qm)呈现25BS50BS100BS特点,升温使qm减小。

关 键 词:两性表面活性剂  阳离子表面活性剂  膨润土  修饰机制
收稿时间:2015/7/23 0:00:00
修稿时间:2015/11/14 0:00:00

Mechanism of CTMAB Modifying BS-12 Modified Bentonite
YU Lu,MENG Zhaofu,LI Wenbin,REN Shuang,WU Qiong,LIU Wei and BAI Dan.Mechanism of CTMAB Modifying BS-12 Modified Bentonite[J].Acta Pedologica Sinica,2016,53(2):543-551.
Authors:YU Lu  MENG Zhaofu  LI Wenbin  REN Shuang  WU Qiong  LIU Wei and BAI Dan
Institution:College of Resource and Environment, Northwest A & F University,College of Resource and Environment, Northwest A & F University,College of Resource and Environment, Northwest A & F University,College of Resource and Environment, Northwest A & F University,College of Resource and Environment, Northwest A & F University,College of Resource and Environment, Northwest A & F University and College of Resource and Environment, Northwest A & F University
Abstract:Mechanism of hexadecyl trimethyl ammonium bromide(CTMA)modifying the surface of dodecyl dimethyl betaine(BS-12)modified bentonite was studied. Judging by changes in the Sum of CTMA and Calcium ion(SCC)on the surface of BS-12 modified bentonite and CTMA adsorption as affected by temperature,20℃or 40℃,it was found that there were two modes of CTMA adsorption on BS-12 modified bentonite:ion exchanging and hydrophobic bonding. On the surface of BS-12 modified bentonites(25BS, 50BS and 100BS)varying in modification degree,25%,50% and 100%,the adsorption of CTMA in the mode of hydrophobic bonding reached its critical level in proportion(RC),that is,20.30%,11.56%and 2.00%,respectively,and the percentage of hydrophobic bonding increased with increasing CTMA modification ratio(R)and mole fraction. The critical ratio(RC′)reached 200%,150% and 100%, respectively,when hydrophobic bonding assumed its absolute dominancy. On the surface of bentonites modified with BS-12 only or with BS-12 and CTMA,50% and 200% was the turning point for hydrophobic bonding to appear and to assume absolute dominancy,Separately. When R < RC,CTMA adsorption was mainly in the ion exchanging mode;when RC ≤ R ≤ RC′,it was in both modes,ion exchanging and hydrophobic bonding;and when R > RC′,it was overwhelmingly dominated with hydrophobic bonding mode. RC、RC′ and the maximum adsorption of CTMA(qm)displayed an order of 25BS>50BS>100BS. With rising temperature,qm declined.
Keywords:Amphoteric surfactants  Cationic surfactants  Bentonite  Modification mechanism
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