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聚邻苯二胺-二氧化硅复合材料的合成与表征:树莓型与核壳型结构。我们的研究现状如何?

Synthesis and characterization of polyaniline-silica composites: Raspberry vs core-shell structures. Where do we stand?

机构信息

Institut UTINAM, UMR CNRS 6213, Univ. Bourgogne Franche-Comté, Equipe Matériaux et Surfaces Fonctionnels, 16 route de Gray, 25030 Besançon Cedex, France.

Institut FEMTO-ST, UMR 6174 CNRS, Univ. Bourgogne Franche-Comté, 15B, Avenue des Montboucons, 25030 Besancon Cedex, France.

出版信息

J Colloid Interface Sci. 2017 Sep 15;502:184-192. doi: 10.1016/j.jcis.2017.04.092. Epub 2017 Apr 29.

Abstract

The synthesis of polyaniline-silica composites has been reinvestigated in view of the opposing results found in the literature. Firstly, we synthesized silica particles with tunable size using the Stöber process. These silica particles have been fully characterized before being used as solid support for the polymerization of aniline. This polymerization was performed according to a published procedure where the pH of the reaction mixture was below the pKa of aniline but at a value where the silica particles surface was still slightly negatively charged. The objective of this procedure was to favor electrostatic interactions between anilinium cations and the silica surface to lead to the formation of silica-polyaniline core-shell particles. Several sets of nanocomposites were prepared under different experimental conditions (oxidant/aniline ratio, silica concentration, temperature, silica particles diameters). The study evidenced that under all the conditions used the formation of core-shell nanoparticles is impossible. However, using different particle sizes, noticeable morphological differences were observed. The use of large silica particles led to the formation of non-uniform polyaniline-silica composites whereas the use of smaller particles always led to raspberry-like morphology as reported by other groups in highly acidic media. The difference in morphology led to different electrical properties with electrical conductivities measured at room temperature ranging from 1.6×10 to 2.5×10S cm.

摘要

重新研究了聚苯胺-二氧化硅复合材料的合成,因为文献中发现了相互矛盾的结果。首先,我们使用 Stöber 法合成了具有可调尺寸的二氧化硅颗粒。在将这些二氧化硅颗粒用作苯胺聚合的固体载体之前,对其进行了充分的表征。聚合是按照已发表的程序进行的,其中反应混合物的 pH 值低于苯胺的 pKa,但在该值下,二氧化硅颗粒表面仍略带负电荷。该程序的目的是有利于苯胺阳离子与二氧化硅表面之间的静电相互作用,从而形成二氧化硅-聚苯胺核壳颗粒。在不同的实验条件下(氧化剂/苯胺比、二氧化硅浓度、温度、二氧化硅颗粒直径)制备了几组纳米复合材料。研究表明,在使用的所有条件下,核壳纳米粒子的形成是不可能的。然而,使用不同的颗粒尺寸,观察到明显的形态差异。使用大的二氧化硅颗粒导致形成不均匀的聚苯胺-二氧化硅复合材料,而使用较小的颗粒总是导致在高度酸性介质中其他小组报告的覆盆子状形态。形态的差异导致不同的电性能,在室温下测量的电导率范围为 1.6×10 到 2.5×10 S cm。

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