首页> 外文会议>Trends in colloid and interface science XXIV >FTIR ATR Study of Adsorption of Trisiloxanes and Hydrocarbon Surfactants at Hydrophobic Solids from Aqueous Solutions
【24h】

FTIR ATR Study of Adsorption of Trisiloxanes and Hydrocarbon Surfactants at Hydrophobic Solids from Aqueous Solutions

机译:FTIR ATR研究水溶液中疏水性固体对三硅氧烷和烃表面活性剂的吸附

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Kinetics of the integrated absorbance in C-H stretch region for ethoxylated trisiloxane and alkyl poly-ethoxylate surfactants on low- and highly hydrophobic surfaces has been measured by Fourier-Transform Infrared spectroscopy (FTIR) in the attenuated total reflection (ATR) mode. It has been found that regardless of the surface energy of substrate the absorbance of trisiloxanes continuously increases during the experiment (characteristic time scale is ten minutes), while the absorbance of alkyl poly-ethoxylate surfactants reaches equilibrium for tens of seconds on low hydrophobic and for a few minutes on the highly hydrophobic surfaces. The continuous growth of absorbance with increasing bulk concentration of surfactants has been detected in the case of trisiloxanes on both substrates even at concentrations above critical wetting concentration; while hydrocarbon surfactants attained the constant values of absorbance at concentrations above critical aggregation concentration. The results for alkyl polyethoxylate surfactants obtained from FTIR-ATR spectra are consistent with the results obtained by other authors used neutron and optical reflectometry. Influence of the length of hydrophilic chains on the value of the absorbance of surfactants has been analyzed. In the case of alkyl polyethoxylate surfactants the absorbance decreases with increasing the length of hydrophilic ethoxy groups. However, in the case of trisiloxane surfactants studied the above trend cannot be clearly traced. Some aspects associated with the relationship between adsorption of trisiloxanes at hydrophobic solid/liquid interfaces and spreading kinetics are discussed.
机译:通过傅立叶变换红外光谱(FTIR)以衰减全反射(ATR)模式测量了低疏水和高疏水表面上乙氧基化三硅氧烷和烷基聚乙氧基表面活性剂在C-H拉伸区的积分吸光度的动力学。已经发现,不管底物的表面能如何,在实验过程中三硅氧烷的吸光度持续增加(特征时间尺度为十分钟),而烷基聚乙氧基表面活性剂的吸光度在低疏水性和在高度疏水的表面上停留几分钟。在三硅氧烷的情况下,即使在高于临界润湿浓度的浓度下,也检测到随着表面活性剂体积浓度的增加,吸光度持续增长。而碳氢化合物表面活性剂在高于临界聚集浓度时达到恒定的吸光度值。从FTIR-ATR光谱获得的烷基聚乙氧基表面活性剂的结果与其他作者使用中子和光学反射法获得的结果一致。分析了亲水链的长度对表面活性剂吸收值的影响。在烷基聚乙氧基化物表面活性剂的情况下,吸光度随亲水性乙氧基长度的增加而降低。但是,在研究三硅氧烷表面活性剂的情况下,上述趋势无法清楚地追踪。讨论了与三硅氧烷在疏水性固/液界面处的吸附与扩散动力学之间的关系有关的一些方面。

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