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Studies of the interaction of gemini surfactants with polymers and triblock copolymers.

机译:研究双子表面活性剂与聚合物和三嵌段共聚物的相互作用。

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The interaction of two novel surfactants, known as gemini surfactants, with aqueous solutions of neutral polymers, specifically polyethylene oxide (PEO), polypropylene oxide (PPO), and polyethylene oxide-polypropylene oxide-polyethylene oxide (PEO-PPO-PEO) triblock copolymers, have been investigated. In order to provide a basis for comparison, an investigation of the aqueous solution behaviour of two series of N,N-bis(alkyldimethyl)-α,ω-alkanedianimonium dibromide surfactants was carried out. One series had a constant spacer length (s) of 3 methylene units with various alkyl chain lengths (m) of 8, 10, 12, and 16, and the other had a constant in of 12 with various s between 2 and 16 inclusive. A surfactant with in = 12 and a p-xylyl (&phis;) spacer also was studied to assess the effect of rigidity in the spacer group on gemini interfacial properties.; The results obtained for the critical micelle concentration (CMC) and head group area (a0) of the surfactants are in excellent agreement with those previously reported. The mean aggregation number of the surfactants decreases with increasing spacer chain length up to s = 8, after which the aggregation number increases. The initial decrease results from a decrease in the surface area available to a surfactant monomer as the area taken up by the spacer group is increased. Experimental apparent molar volume (AMV) data have been modeled assuming both a mass-action model (8-3-8, only) and a pseudo-phase model. The observed variation in the volume change due to micelle formation, ΔV&phis;,M, is consistent with variations in ao and the CMC, and can be rationalized in terms of possible spacer conformations in the aqueous and micellar phases. Results obtained for the 12-&phis;-12 surfactant indicate that rigidity of the spacer has no measurable effect on the micellization process for shorter spacer lengths.; The interaction of the gemini surfactants with the triblock copolymers in aqueous solution was markedly different from that typically observed in surfactant-polymer systems, and is similar in nature to a solubilization or mixed micelle formation process. The results obtained indicate that the interaction occurs primarily with the PPO segment of the triblock copolymer through a replacement of hydration water by polymer at the micellar surface. The solubility of the surfactant monomer (i.e. the CMC) may be increased through specific interactions between the surfactant and polymeric microdomains in solution. The results of a temperature dependent study indicate that the aggregation state of the copolymer in solution has a significant effect on the interaction with gemini surfactants.
机译:两种新型表面活性剂(称为双子表面活性剂)与中性聚合物,特别是聚环氧乙烷(PEO),聚环氧丙烷(PPO)和聚环氧乙烷-聚环氧丙烷-聚环氧乙烷(PEO-PPO-PEO)三嵌段共聚物的水溶液相互作用,已被调查。为了提供比较的基础,对两种N,N′′′-super-双(烷基二甲基)-α,ω-链烷二亚胺二溴化物表面活性剂的水溶液行为进行了研究。一个系列具有3个亚甲基单元的恒定间隔长度(一个或多个),各种烷基链长(m)为8、10、12和16,另一个系列具有12的恒定in,两个s介于2和16之间(含两个端点)。还研究了in = 12和-二甲苯基(φ)间隔基的表面活性剂,以评估间隔基的刚性对双子界面性能的影响。表面活性剂的临界胶束浓度(CMC)和头基面积(a 0 )获得的结果与以前报道的结果非常一致。表面活性剂的平均聚集数随着间隔链长度的增加而降低,直至s = 8,此后聚集数增加。最初的减少是由于随着间隔基团所占的面积增加,表面活性剂单体可利用的表面积减少而导致的。假设质量作用模型(仅适用于8-3-8)和伪相模型,对实验视在摩尔体积(AMV)数据进行了建模。观察到的由于胶束形成而引起的体积变化的变化ΔVφ,M 与ao和CMC的变化一致,并且可以根据水溶液和胶束中可能的间隔子构象进行合理化处理。阶段。对于12-φ-12表面活性剂获得的结果表明,对于较短的间隔物长度,间隔物的刚度对胶束化过程没有可测量的影响。双子表面活性剂与三嵌段共聚物在水溶液中的相互作用与表面活性剂-聚合物体系中通常观察到的相互作用显着不同,并且本质上类似于增溶或混合胶束形成过程。获得的结果表明,相互作用主要通过胶束表面的聚合物代替水合水而与三嵌段共聚物的PPO链段发生。表面活性剂单体(即CMC)的溶解度可通过表面活性剂与溶液中的聚合物微区之间的特定相互作用而增加。温度依赖性研究的结果表明,溶液中共聚物的聚集状态对与双子表面活性剂的相互作用具有显着影响。

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