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膨润土对复合污染中表面活性剂的吸附及机理
引用本文:孙晓慧,卢瑛莹,陈曙光,李灵剑,沈学优.膨润土对复合污染中表面活性剂的吸附及机理[J].环境科学,2007,28(4):838-842.
作者姓名:孙晓慧  卢瑛莹  陈曙光  李灵剑  沈学优
作者单位:1. 浙江大学环境科学系,杭州,310028;浙江省环境监测中心,杭州,310012
2. 浙江省环境保护科学设计研究院,杭州,310007
3. 浙江大学环境科学系,杭州,310028
4. 杭州电子科技大学机电工程分院,杭州,310018
基金项目:国家自然科学基金项目(50378081,20477036);浙江省科技计划项目(2005F13013)
摘    要:选取阳离子表面活性剂氯化十六烷基吡啶(CPC)、阴离子表面活性剂十二烷基苯磺酸钠(SDBS)及非离子表面活性剂Triton X-100(TX-100)为代表,研究了其在膨润土上的吸附行为,探讨了膨润土阳离子交换容量(CEC)、温度、盐度对CPC吸附的影响.结果表明,Na基膨润土对CPC的吸附性能最好,对SDBS基本无吸附,对TX-100的吸附介于两者之间.Na基膨润土对CPC的吸附是阳离子交换和疏水键缔合共同作用的结果,对TX-100的吸附主要是通过其与膨润土硅氧表面间的氢键作用,同时通过疏水键作用形成吸附双分子层;SDBS在Ca基膨润土上的吸附损失量先增大后减小,在1.5倍临界胶束浓度 (CMC)时达到极大值,主要机理是SDBS与膨润土中的Ca2+产生沉淀作用,而胶束具有再溶解沉淀的作用.膨润土对CPC的吸附量随着温度升高而降低,随着CEC的增大而增大,一定浓度NaCl的加入有利于其在膨润土上的吸附.

关 键 词:膨润土  吸附  阳离子交换容量(CEC)  氯化十六烷基吡啶(CPC)  十二烷基苯磺酸钠(SDBS)  Triton  X-100(TX-100)
文章编号:0250-3301(2007)04-0838-05
收稿时间:2006/5/18 0:00:00
修稿时间:2006-05-182006-06-25

Sorption and Mechanism of Surfactants on Bentonite in Combined Pollution
SUN Xiao-hui,LU Ying-ying,CHEN Shu-guang,LI Ling-jian and SHEN Xue-you.Sorption and Mechanism of Surfactants on Bentonite in Combined Pollution[J].Chinese Journal of Environmental Science,2007,28(4):838-842.
Authors:SUN Xiao-hui  LU Ying-ying  CHEN Shu-guang  LI Ling-jian and SHEN Xue-you
Institution:Department of Environmental Science, Zhejiang University, Hangzhou 310028, China. sxh_1119@163.com
Abstract:Sorption of cationic surfactant cetyl pyridinium chloride (CPC), anionic surfactant sodium dodecylbenzene sulfonate (SDBS) and nonionic surfactant Triton X-100(TX-100) on bentonite was studied. The influences of cation-exchange capacity (CEC), temperature and salinity on the sorption of CPC were also discussed. The results indicate that the sorption of CPC on Na-bentonite is greater than that of TX-100 and SDBS, and SDBS hardly shows any sorption. CPC is adsorbed to Na-bentonite through a combination of hydrophobic bonding and cation-exchange. While TX-100 is adsorbed to Na-bentonite via the formation of an adsorption layer of twain surfactant molecule and hydrogenolysis of silicon-oxygen surface of bentonite and TX-100. The amount of SDBS adsorbed on Ca-bentonite increases with increasing surfactant concentration, reaching a maximum at 1.5 critical micelle concentration (CMC), and then decreases with increasing surfactant loading. The mechanism of the retention appears to be formation of a sparingly soluble Ca-SDBS species, and dissolution in the micelle. The amount of CPC adsorbed on bentonite decreases with increasing temperature, and increases with increasing CEC. NaCl can enhance the sorption of CPC on bentonite.
Keywords:bentonite  sorption  cation-exchange capacity(CEC)  cetyl pyridinium chloride(CPC)  sodium dodecylbenzene sulfonate(SDBS)  Triton X(TX-100)
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