首页> 外文学位 >Adsorption of anionic surfactants on polystyrene latex surfaces.
【24h】

Adsorption of anionic surfactants on polystyrene latex surfaces.

机译:阴离子表面活性剂在聚苯乙烯胶乳表面上的吸附。

获取原文
获取原文并翻译 | 示例

摘要

The adsorption of several anionic surfactants on polystyrene latexes of variable surface charge density was studied to provide a comprehensive understanding of the effects of surface charge density on surfactant adsorption. Adsorbed amounts were determined from direct analysis of the bulk surfactant concentration using ion chromatography. The data indicates that the relationship between adsorbed amount and surface charge density is more complex than previously believed.;The results suggest that as the surface charge density of the same sign as the adsorbing species increases, the adsorbed amount initially increases at very low surface potentials (0 to ;Analysis of two-component adsorption indicated that when anionic surfactants compete for an adsorbing surface, the adsorbed amount is greater than observed in the single component adsorption situations. This is true even for weakly adsorbed surfactants, and is presumably due to initially adsorbed surfactant causing enhanced chain-on-chain adsorption which results in higher adsorbed amounts. This effect is particularly evident for a two-tailed surfactant, since one of the hydrophobic tails may be free and available for adsorption while the other is attached to the surface. Displacement adsorption results displayed no significant change from the competitive adsorption cases because no displacement was occurring. This was found to be due to the enhanced chain-on-chain adsorption which resulted in increased adsorbed amounts identical to the coadsorption situation.
机译:研究了几种阴离子表面活性剂在可变表面电荷密度的聚苯乙烯胶乳上的吸附,以提供对表面电荷密度对表面活性剂吸附影响的全面理解。吸附量是通过使用离子色谱法直接分析整体表面活性剂浓度来确定的。数据表明,吸附量与表面电荷密度之间的关系比以前认为的要复杂。;结果表明,随着与吸附物相同的符号的表面电荷密度的增加,在非常低的表面电势下吸附量最初会增加(0到;对两组分吸附的分析表明,当阴离子表面活性剂争夺吸附表面时,吸附量大于在单组分吸附情况下观察到的吸附量。即使对于弱吸附的表面活性剂也是如此,这可能是由于最初吸附的表面活性剂增强了链上链的吸附能力,从而增加了吸附量,这种效果在两尾表面活性剂中尤为明显,因为其中一个疏水尾巴可能是自由的,可用于吸附,而另一个则附着在表面上。位移吸附结果与竞争吸附情况相比没有显着变化。因为没有发生位移。发现这是由于增强的链上链吸附,这导致增加的吸附量与共吸附情况相同。

著录项

  • 作者

    Hoeft, Carl Edward.;

  • 作者单位

    Washington State University.;

  • 授予单位 Washington State University.;
  • 学科 Chemical engineering.;Polymer chemistry.;Organic chemistry.
  • 学位 Ph.D.
  • 年度 1994
  • 页码 162 p.
  • 总页数 162
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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