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首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Dual pH- and Light-Responsive Amphiphilic Random Copolymer Nanomicelles as Particulate Emulsifiers to Stabilize the Oil/Water Interface
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Dual pH- and Light-Responsive Amphiphilic Random Copolymer Nanomicelles as Particulate Emulsifiers to Stabilize the Oil/Water Interface

机译:双pH-和光响应式两亲的无规共聚物纳米作为颗粒乳化剂稳定油/水界面

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Dual pH- and light-responsive nanomicelles self assembled from amphiphilic random poly(methacrylic acid-co-methyl methacrylate-co-7-(4-vinylbenzyloxyl)-4-methylcoumarin) (P(MAA-co-MMA-co-VM)) have been successfully prepared and employed as particulate emulsifiers to stabilize the oil/water interface. The self assembling behavior of copolymers in a selective solvent is explored. The structural transitions of CP55 micelles based on a copolymer with 55 mol % hydrophilic methacrylic acid units are investigated by the dosage of ultraviolet irradiation and pH variation. As pH increases, the ionization of the carboxyl groups leads to the swelling of micelles. Both the size and polydispersity index of cross-linked micelles are far larger than those of un-cross-linked micelles under alkaline conditions. The comparison of the configuration of the un-cross-linked micelles and cross-linked micelles at the oil/water interface is investigated by scanning electron microscopy. The results show that the ability of swelling and conformational changing in response to external pH- and light-triggers largely affected the emulsifying performance of the particulate emulsifiers. Especially for emulsions stabilized by the cross-linked micelles, oil begins to separate out as pH elevated over 7.3 on account of the restricted conformational adjustment that resulted from the increasing interparticle cross-linking and electrostatic repulsion. The findings may be useful for challenging industrial areas where organic macromolecules and surfactants cooperate.
机译:从两亲型无规聚(甲基丙烯酸 - 共聚甲基丙烯酸甲酯-CO-7-(4-乙烯基苯并氧基)-4-甲基伞素)(P(MAA-CO-MMA-CO-VM)中的双pH-和光响应纳米钙已经成功制备并使用作为颗粒乳化剂以稳定油/水界面的颗粒乳化剂。探讨了在选择性溶剂中的共聚物的自组装行为。基于共聚物的CP55胶束的结构转变通过紫外线辐照和pH变异剂的剂量研究了55mol%亲水性甲基丙烯酸单元。作为pH增加,羧基的电离导致胶束的溶胀。交联胶束的尺寸和多分散性指数远远大于碱性条件下的未交联胶束的尺寸和多分散性指数。通过扫描电子显微镜研究了油/水界面处的联合连接胶束和交联胶束的结构的比较。结果表明,响应外部pH和光触发器的溶胀和构象变化的能力在很大程度上影响了颗粒乳化剂的乳化性能。特别是对于通过交联胶束稳定稳定的乳液,油开始分离,因为由于增加的颗粒交联和静电排斥而导致的限制构象调整,以7.3升高7.3。该发现对于挑战有机大分子和表面活性剂配合的挑战工业区。

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