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分散体系中的聚合物表面活性剂。

Polymeric surfactants in disperse systems.

作者信息

Tadros Tharwat

机构信息

89 Nash Grove Lane, Wokingham, Berkshire RG40 4HE, UK.

出版信息

Adv Colloid Interface Sci. 2009 Mar-Jun;147-148:281-99. doi: 10.1016/j.cis.2008.10.005. Epub 2008 Nov 5.

Abstract

This overview starts with a section on general classification of polymeric surfactants. Both homopolymers, block and graft copolymers are described. The solution properties of polymeric surfactants is described by using the Flory-Huggins theory. Particular attention is given to the effect of solvency of the medium for the polymer chains. The adsorption and conformation of homopolymers, block and graft copolymers at the solid/liquid interface is described. The theories of polymer adsorption and their predictions are briefly described. This is followed by a description of the experimental techniques that can be applied to study polymeric surfactant adsorption. Examples of adsorption isotherms of non-ionic polymeric surfactants are given. The effect of solvency on the adsorption amount is also described. Results for the adsorbed layer thickness of polymeric surfactants are given with particular attention to the effect of molecular weight. The interaction between particles containing adsorbed layers is described in terms of the unfavorable mixing of the stabilizing chains when these are in good solvent conditions. The entropic, volume restriction or elastic interaction that occurs on considerable overlap is also described. Combination of these two effects forms the basis of the theory of steric stabilization. The energy-distance curve produced with these sterically stabilized systems is described with particular attention of the effect of the ratio of adsorbed layer thickness to droplet radius. Examples of oil-in-water (O/W) and water-in-oil (W/O) emulsions stabilized with polymeric surfactants are given. Of particular interest is the O/W emulsions stabilized using hydrophobically modified inulin (INUTEC((R))SP1). The emulsions produced are highly stable against coalescence both in water and high electrolyte concentrations. This is accounted for by the multipoint attachment of the polymeric surfactant to the oil droplets with several alkyl groups and the strongly hydrated loops and tails of linear polyfructose. Evidence of this high stability was obtained from disjoining pressure measurements. Stabilization of suspensions using INUTEC((R))SP1 was described with particular reference to latexes that were prepared using emulsion polymerization. The high stability of the latexes is attributed to the strong adsorption of the polymeric surfactant on the particle surfaces and the enhanced steric stabilization produced by the strongly hydrated polyfructose loops and tails. Evidence for such high stability was obtained using Atomic Force Microscopy (AFM) measurements. The last part of the overview described the preparation and stabilization of nano-emulsions using INUTEC((R))SP1. In particular the polymeric surfactant was very effective in reducing Ostwald ripening as a result of its strong adsorption and the Gibbs elasticity produced by the polymeric surfactant.

摘要

本综述开篇是关于聚合物表面活性剂的一般分类部分。介绍了均聚物、嵌段共聚物和接枝共聚物。利用弗洛里 - 哈金斯理论描述了聚合物表面活性剂的溶液性质。特别关注了介质对聚合物链的溶解能力的影响。描述了均聚物、嵌段共聚物和接枝共聚物在固/液界面的吸附和构象。简要介绍了聚合物吸附理论及其预测。接下来描述了可用于研究聚合物表面活性剂吸附的实验技术。给出了非离子型聚合物表面活性剂的吸附等温线示例。还描述了溶解能力对吸附量的影响。给出了聚合物表面活性剂吸附层厚度的结果,特别关注了分子量的影响。当稳定链处于良溶剂条件下时,从稳定链的不利混合角度描述了含吸附层颗粒之间的相互作用。还描述了在大量重叠时发生的熵、体积限制或弹性相互作用。这两种效应的结合构成了空间稳定理论的基础。描述了由这些空间稳定体系产生的能量 - 距离曲线,特别关注了吸附层厚度与液滴半径之比的影响。给出了用聚合物表面活性剂稳定的水包油(O/W)和油包水(W/O)乳液的示例。特别令人感兴趣的是用疏水改性菊粉(INUTEC®SP1)稳定的O/W乳液。所制备的乳液在水和高电解质浓度下对聚结都具有高度稳定性。这是由于聚合物表面活性剂通过几个烷基与油滴的多点附着以及线性聚果糖的强水合环和尾部造成的。通过分离压力测量获得了这种高稳定性的证据。描述了使用INUTEC®SP1对悬浮液的稳定作用,特别提及了通过乳液聚合制备的胶乳。胶乳的高稳定性归因于聚合物表面活性剂在颗粒表面的强烈吸附以及由强水合聚果糖环和尾部产生的增强的空间稳定作用。使用原子力显微镜(AFM)测量获得了这种高稳定性的证据。综述的最后一部分描述了使用INUTEC®SP1制备和稳定纳米乳液的过程。特别是这种聚合物表面活性剂由于其强烈吸附以及聚合物表面活性剂产生的吉布斯弹性,在减少奥斯特瓦尔德熟化方面非常有效。

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