首页 | 本学科首页   官方微博 | 高级检索  
     检索      

醇对SDS-CTAB-H2O体系双水相性质的影响
引用本文:尚亚卓,刘洪来,胡英.醇对SDS-CTAB-H2O体系双水相性质的影响[J].华东理工大学学报(自然科学版),2004,30(6):661-664.
作者姓名:尚亚卓  刘洪来  胡英
作者单位:华东理工大学化学系,国家重点化学工程联合实验室,上海,200237;华东理工大学化学系,国家重点化学工程联合实验室,上海,200237;华东理工大学化学系,国家重点化学工程联合实验室,上海,200237
基金项目:国家自然科学基金(20025618,20236010);上海市教委资助项目
摘    要:研究了短链一元醇(乙醇、正丁醇)和二元醇(乙二醇、1,4—丁二醇)对正负离子表面活性剂混合溶液(十二烷基硫酸钠—十六烷基三甲基溴化铵—水)双水相的影响。结果表明:一元醇的加入不但缩短了双水相的成相时间、使原水溶液双水相的区域得到扩展而且还会导致新双水相区域的出现,这种影响随着醇类链长的增长而增大。而二元醇的加入对双水相的相图影响不大,只是对形成双水相的表面活性剂最低总浓度稍有影响。实验结果也表明,出现双水相的表面活性剂最低总浓度与混合溶液的临界胶束浓度(CMC)有关,但CMC并不是决定出现双水相表面活性剂最低浓度的唯一因素。

关 键 词:一元醇  二元醇  双水相  正负离子表面活性剂
文章编号:1006-3080(2004)06-0661-04
修稿时间:2003年11月5日

The Effect of Various Alcohols on the Aqueous Two-phase System of Cationic and Anionic Surfactants
SH ANG Ya-zhuo,L IU H ong-lai,H U Ying.The Effect of Various Alcohols on the Aqueous Two-phase System of Cationic and Anionic Surfactants[J].Journal of East China University of Science and Technology,2004,30(6):661-664.
Authors:SH ANG Ya-zhuo  L IU H ong-lai  H U Ying
Institution:SH ANG Ya-zhuo,L IU H ong-lai*,H U Ying
Abstract:The effect of short chain monohydric alcohols (ethanol, n-butanol) and dihydric alcohols (ethyleneglycol, 1,4-butanediol) on the aqueous two-phase system (ATPS) of cationic and anionic surfactants (SDS-CTAB) is studied. Results show that the additions of monohydric alcohols can not only shorten the phase separation time, expand the regions of ATPS but also cause the formation of a new kind of ATPS compared with original aqueous solutions. At the same time the effect becomes more obvious when the chain length of alcohol is getting longer. However, the dihydric alcohols have little effect on the diagram of ATPS. Experimental results also show that the CMC of the mixed solution has something to do with the lowest concentration of surfactants under which the ATPS can form, but CMC is not the only factor.
Keywords:monohydric alcohol  dihydric alcohol  aqueous two-phase system (ATPS)  cationic and anionic surfactant
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号