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Synthesis of Polymeric (Nano)Capsules Based on Dopamine and Derivatives Using Emulsion Templating

机译:乳化模板法合成基于多巴胺及其衍生物的高分子(纳米)胶囊

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摘要

A soft-templating method has been developed for the synthesis of hollow polymer (nano)capsules comprising dopamine and derivatives. The method involves the use of an aqueous emulsion comprising toluene or cyclohexane droplets as templates. Dopamine (and derivatives) polymerization is conducted at room temperature in the aqueous phase and/or at the droplet surfaces, thus forming hollow polymer (nano)capsules. Dialysis was demonstrated to be an effective technique for removal of surfactant, hexadecane and unreacted monomer without destroying the capsule structure and introducing other materials. This method demonstrates that emulsion droplets can serve as templates with advantages of high stability, small size and straight-forward elimination. By using this method, the shell thickness can be readily tuned by adjusting the initial amount of monomer. Nanocapsules of diameters as low as ~50 nm can be readily prepared using this novel approach. When using Shirasu porous glass (SPG) membrane emulsification to produce emulsion templates, the capsule size can be tuned easily by applying different pore size membranes. Attempts were made to functionalize the capsules - silver nanoparticles were explored for encapsulation within the capsules via miniemulsion templating. A simple method was employed to produce monodisperse fine silver nanoparticles of approximate diameters 10 nm. However, encapsulation proved to be extremely challenging. It is believed that the difficulties were caused by side reactions between components of the silver nanoparticle synthesis step and the polymerization step. Overall, the work presented represents a creative one-step method providing a new approach to the synthesis of hollow polymer (nano)capsules comprising dopamine and derivatives, which has the potential to dramatically expand their commercial applications.
机译:已经开发了一种软模板方法来合成包含多巴胺和衍生物的中空聚合物(纳米)胶囊。该方法涉及使用包含甲苯或环己烷液滴作为模板的水性乳液。多巴胺(和衍生物)聚合是在室温下在水相和/或液滴表面进行的,从而形成中空的聚合物(纳米)胶囊。透析被证明是去除表面活性剂,十六烷和未反应的单体而不破坏胶囊结构和引入其他材料的有效技术。该方法证明乳液液滴可以用作模板,具有高稳定性,小尺寸和直接消除的优点。通过使用该方法,可以通过调节单体的初始量来容易地调节壳的厚度。使用这种新方法可以轻松制备直径低至〜50 nm的纳米胶囊。当使用Shirasu多孔玻璃(SPG)膜乳化法生产乳剂模板时,可以通过使用不同孔径的膜轻松调整胶囊的大小。尝试使胶囊功能化-通过纳米乳液模板研究了银纳米颗粒用于胶囊内的封装。采用一种简单的方法来生产直径约10 nm的单分散细银纳米​​颗粒。然而,封装被证明是极具挑战性的。认为困难是由银纳米颗粒合成步骤和聚合步骤的组分之间的副反应引起的。总体而言,提出的工作代表了一种创新的一步法,为合成包含多巴胺和衍生物的中空聚合物(纳米)胶囊提供了一种新方法,这有望极大地扩展其商业应用。

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