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制备非水高内相比Pickering乳液:添加聚合物和选择性干燥的影响

Making non-aqueous high internal phase pickering emulsions: influence of added polymer and selective drying.

作者信息

Cai Dongyu, Thijssen Job H T, Clegg Paul S

机构信息

SUPA, School of Physics and Astronomy, University of Edinburgh , Mayfield Road, Edinburgh EH9 3JZ, United Kingdom.

出版信息

ACS Appl Mater Interfaces. 2014 Jun 25;6(12):9214-9. doi: 10.1021/am501328r. Epub 2014 Jun 4.

Abstract

We report the first example of a non-aqueous (oil-in-oil) Pickering high internal phase emulsion (HIPE) stabilized by chemically modified fumed silica. In this case, a 75 vol % ethylene carbonate (EC)-rich internal phase is emulsified in 25 vol % p-xylene (xylene)-rich continuous phase using interfacial nanoparticles. It is revealed that no phase inversion takes place during the HIPE formation process when using the appropriate wettability of solid particles. Incorporating polystyrene (PS) into xylene enables one-step formation of PS-filled HIPEs in place of a multi-step polymerization of the continuous phase. We observe that the size of droplets changes with the addition of PS, and we associate this with the change in the viscosity of the continuous xylene-rich phase. Drying the pure HIPE results in the selective removal of xylene and coalescence of EC-rich droplets. With the PS in the xylene-rich continuous phase, we show that EC-rich droplets can be retained even though the xylene is evaporated off, and a new semi-solid composite containing both liquid phase and solid phase is formed via this non-aqueous Pickering-HIPE template.

摘要

我们报道了首例由化学改性气相二氧化硅稳定的非水(油包油)皮克林高内相乳液(HIPE)。在这种情况下,使用界面纳米颗粒将富含75体积%碳酸亚乙酯(EC)的内相乳化在富含25体积%对二甲苯(二甲苯)的连续相中。结果表明,当使用具有适当润湿性的固体颗粒时,在HIPE形成过程中不会发生相转变。将聚苯乙烯(PS)加入二甲苯中能够一步形成填充有PS的HIPE,而无需连续相的多步聚合。我们观察到液滴尺寸随PS的添加而变化,并且我们将此与富含二甲苯的连续相的粘度变化联系起来。干燥纯HIPE会导致二甲苯的选择性去除以及富含EC的液滴聚结。对于富含二甲苯的连续相中含有PS的情况,我们表明即使二甲苯蒸发掉,富含EC的液滴仍可保留,并且通过这种非水皮克林-HIPE模板形成了一种包含液相和固相的新型半固体复合材料。

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