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Studies on Adsorption and Wetting Phenomena Associated with Solid Surfaces in Aqueous Synthetic and Natural Surfactant Solutions

机译:合成和天然表面活性剂水溶液中固体表面的吸附和润湿现象研究

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摘要

Adsorption of surfactants at air-liquid and solid-liquid interface and wetting of solid surfaces are closely interdependent. The performance of many physicochemical process and fundamental understanding depends on these two important phenomena. Because of the importance of these phenomena this study mainly focuses on adsorption of different surfactants at air-water and solid-water interfaces and wetting of those surfactant solutions at flat solid surfaces. The main emphasis of this study is plant-based natural surfactants; however some synthetic surfactants are also studied as a reference for comparison. The effects of electrolytes, alcohols, and naturalsynthetic surfactants mixtures are also studied. Electrolytes are most powerful inexpensive additive enhances the adsorption capacity of ionic surfactants at interfaces which in turn also enhances the interfacial behaviour. Adsorption kinetics and isotherm of anionic (dodecylbenzene sulfonate, SDBS), cationic (cetylpyridinium bromide, CPB), and non-ionic (TX-100) surfactants in the presence and absence of electrolytes on PTFE-water interface are studied. The kinetics of adsorption fits well pseudo-second-order kinetic model for the three surfactants studied here. Adsorption isotherms of TX-100 follow Langmuir type, whereas SDBS and CPB follow Freundlich type. However, in the presence of electrolytes both the ionic surfactants show better fitting with Langmuir type isotherm. The effect of electrolytes on the surfactant concentration far below the CMC shows there is a linear increase in amount adsorbed with the increase in ionic strength of the electrolyte mainly due to reduction in headgroup repulsion and finally reaches a plateau level when the equilibrium concentration reaches CMC at that electrolyte concentration. The structure of tailgroup of non-ionic surfactants also plays an important role in both adsorption and wetting behaviour. To get some insight about the fact, the adsorption and wetting behavior of two nonionic surfactants (TX-100 and Igepal CO-630) having the same headgroup but structurally different tailgroups has been compared. The change in contact angle with the concentration of surfactant follows a trend similar to that for adsorption onto a PTFE surface. At low surfactant concentration, Igepal CO-630 shows a slightly higher adsorption density and better wetting properties than TX-100. Both surfactants show lower adsorption densities at the PTFE–water interface than at the air–water interface.
机译:表面活性剂在气-液和固-液界面的吸附与固体表面的润湿紧密相关。许多物理化学过程的执行和基本理解取决于这两个重要现象。由于这些现象的重要性,本研究主要集中在空气-水和固体-水界面上不同表面活性剂的吸附以及平坦固体表面上这些表面活性剂溶液的润湿。这项研究的重点是基于植物的天然表面活性剂。但是,也研究了一些合成表面活性剂作为比较的参考。还研究了电解质,醇和天然合成表面活性剂混合物的影响。电解质是最强大的廉价添加剂,可增强离子型表面活性剂在界面处的吸附能力,进而增强界面行为。研究了在PTFE-水界面上是否存在电解质的情况下,阴离子型(十二烷基苯磺酸盐,SDBS),阳离子型(十六烷基溴化吡啶,CPB)和非离子型(TX-100)表面活性剂的吸附动力学和等温线。吸附的动力学非常适合本文研究的三种表面活性剂的拟二级动力学模型。 TX-100的吸附等温线遵循Langmuir类型,而SDBS和CPB遵循Freundlich类型。但是,在存在电解质的情况下,两种离子表面活性剂都显示出与Langmuir型等温线的更好拟合。电解质对远低于CMC的表面活性剂浓度的影响表明,吸附量随电解质的离子强度的增加呈线性增加,这主要是由于头基团排斥力的降低,并且最终在平衡浓度达到CMC时达到稳定水平。电解质浓度。非离子表面活性剂的尾基结构在吸附和润湿行为中也起着重要作用。为了了解这一事实,已比较了具有相同头基但结构不同尾基的两种非离子表面活性剂(TX-100和Igepal CO-630)的吸附和润湿行为。接触角随表面活性剂浓度的变化遵循与吸附到PTFE表面相似的趋势。在低表面活性剂浓度下,Igepal CO-630与TX-100相比,显示出更高的吸附密度和更好的润湿性能。两种表面活性剂在PTFE-水界面处的吸附密度均低于在空气-水界面处的吸附密度。

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    Biswal Nihar Ranjan;

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  • 年度 2012
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