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作为微乳液增效剂的亲水性醇乙氧基化物

Hydrophilic alcohol ethoxylates as efficiency boosters for microemulsions.

作者信息

Frank Christian, Frielinghaus Henrich, Allgaier Jürgen, Richter Dieter

机构信息

Institut für Festkörperforschung, Forschungszentrum Jülich GmbH, 52425 Jülich, Germany.

出版信息

Langmuir. 2008 Jun 17;24(12):6036-43. doi: 10.1021/la800360m. Epub 2008 May 24.

Abstract

Highly amphiphilic polyalkane-PEO diblock copolymers drastically increase the solubilization capacity of surfactants in microemulsions if they are used in small quantities as additive to the surfactant. This effect goes along with an additional reduction of the already very low interfacial tension between water and oil. Lamellar phases, which usually develop when the surfactant becomes more efficient, are suppressed to a large extent. In this work we use another type of additive, namely hydrophilic alcohol ethoxylates. These amphiphiles are identical with the previously used block copolymers with respect to the hydrophilic moiety. However, they contain only small hydrocarbon groups ranging from C8 to C18. A typical example from the hydrophilic alcohol ethoxylates is C12E100. Both additive types increase surfactant efficiency equally with respect to mass fraction in the mixture. Because the alcohol ethoxylate additives decorate the surfactant film only on the aqueous side, they influence the curvature of the surfactant membrane or, in other words, the temperature behavior of the microemulsion. Together with nonionic surfactants, however, the shift of the one-phase region to higher temperatures is only a few degrees Celsius. Just as with the polyalkane-PEO block copolymers, the hydrophilic alcohol ethoxylates suppress lamellar phases. This behavior is especially pronounced if the hydrophobic groups are small or the PEO chains are long. We found that hydrophobic units as short as C 8 are sufficient to largely anchor the PEO chains at the interface. If C12 or C18 hydrocarbon unit are used instead, the PEO chains are fully interfacially active, even if the hydrophilic chain contains up to about 500 EO units. We applied the new additives in bicontinuous and in droplet microemulsions and used nonionic, as well as ionic, surfactants, namely C10E4 and AOT. In contrast to polyalkane-PEO blockcopolymers the new additives are easy to synthesize and are commercially available. Therefore, they might be interesting in applications.

摘要

如果将高度两亲性的聚烷烃-聚环氧乙烷二嵌段共聚物作为添加剂少量添加到表面活性剂中,它会显著提高微乳液中表面活性剂的增溶能力。这种效果伴随着水和油之间本就很低的界面张力的进一步降低。通常在表面活性剂效率提高时形成的层状相在很大程度上受到抑制。在这项工作中,我们使用了另一种添加剂,即亲水性醇乙氧基化物。这些两亲物在亲水部分与先前使用的嵌段共聚物相同。然而,它们仅含有从C8到C18的小烃基。亲水性醇乙氧基化物的一个典型例子是C12E100。两种添加剂类型在混合物中的质量分数方面同等程度地提高了表面活性剂效率。由于醇乙氧基化物添加剂仅在水相一侧修饰表面活性剂膜,它们会影响表面活性剂膜的曲率,或者换句话说,影响微乳液的温度行为。然而,与非离子表面活性剂一起时,单相区域向更高温度的转变仅为几摄氏度。就像聚烷烃-聚环氧乙烷嵌段共聚物一样,亲水性醇乙氧基化物会抑制层状相。如果疏水基团小或聚环氧乙烷链长,这种行为会特别明显。我们发现短至C8的疏水单元就足以将聚环氧乙烷链在很大程度上锚定在界面处。如果使用C12或C18烃单元,即使亲水链包含多达约500个环氧乙烷单元,聚环氧乙烷链也具有完全的界面活性。我们将新添加剂应用于双连续和液滴微乳液中,并使用了非离子以及离子表面活性剂,即C10E4和AOT。与聚烷烃-聚环氧乙烷嵌段共聚物不同,新添加剂易于合成且可商购。因此,它们在应用中可能会很有吸引力。

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