...
首页> 外文期刊>Journal of Colloid and Interface Science >The effect of structural variation of alcohols on water solubilization in nonionic microemulsions - 2. Branched alcohols as solubilization modifiers: Results and interpretation
【24h】

The effect of structural variation of alcohols on water solubilization in nonionic microemulsions - 2. Branched alcohols as solubilization modifiers: Results and interpretation

机译:醇的结构变化对非离子型微乳液中水增溶的影响-2.支链醇作为增溶改性剂:结果与解释

获取原文
获取原文并翻译 | 示例
           

摘要

In this second part of a paper dealing with the effect of branched alcohols on solubilization, an attempt has been made to provide explanations of experimental data related mostly to the system Brij 97/branched alcohol + dodecane = 1:1 (by weight)/water at 27 +/- 0.2 degrees C. Applying the Hou-Shah mechanism it was shown that for many C-4-C-6 branched alcohol isomers having one methyl branch, solubilization behavior is readily interpreted by assuming control of the critical radius, R-c. Two parameters, both included in the definition of the branching factor, F-b (which was treated in the first part of the paper), were also used to analyze solubilization data. The first, l(i), is defined as the distance from the free end of the alcohol molecule to the methyl branch. The second, d, is virtually N-A, the chain length of the alcohol. When l(i) > 3, the solubilization becomes dominated by the natural radius Of Curvature, R-0. Also, we have suggested that for R-c-control, solubilization will be enhanced in direct proportion to the distance d-l(i), whereas for R-0-control, solubilization will increase with decreasing d-l(i). The validity of our assumptions was demonstrated in many cases. Some examples of the more complicated case of double branching (two methyl groups along the alcohol chain) were also analyzed. (c) 2005 Elsevier Inc. All rights reserved.
机译:在该论文的第二部分中,涉及支链醇对增溶的影响,尝试提供与系统Brij 97 /支链醇+十二烷= 1:1(按重量计)/水有关的实验数据的解释。在27 +/- 0.2摄氏度下。应用Hou-Shah机理表明,对于许多具有一个甲基支链的C-4-C-6支链醇异构体,通过假定临界半径Rc的控制,很容易解释增溶行为。 。两个参数(均包含在支化因子的定义中)F-b(已在本文的第一部分中进行了处理)也用于分析增溶数据。首先,l(i)定义为从醇分子的自由端到甲基支链的距离。第二个d实际上是N-A,即醇的链长。当l(i)> 3时,增溶作用由曲率的自然半径R-0决定。同样,我们已经建议,对于R-c-控制,增溶将与距离d-1(i)成正比,而对于R-0-控制,增溶将随着d-1(i)的减少而增加。我们的假设在许多情况下都是正确的。还分析了更复杂的双支链情况(沿醇链有两个甲基)的一些例子。 (c)2005 Elsevier Inc.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号