首页 | 本学科首页   官方微博 | 高级检索  
检索        


Rational design of a polypyrrole-based competent bifunctional magnetic nanocatalyst
Authors:Wael A Amer  Basel Al-saida  Mohamad M Ayad
Institution:Chemistry Department, Faculty of Science, Tanta University, Tanta 31527 Egypt ; Chemistry Department, Faculty of Science, Al-Balqa Applied University, Al-Salt 19117 Jordan ; Institute of Basic and Applied Sciences, Egypt-Japan University of Science and Technology, New Borg El-Arab City Alexandria 21934 Egypt, Fax: +20 3 459 9520, +20 3 459 9520
Abstract:The combination of conducting polymers with semiconductors for the fabrication of organic/inorganic hybrid nanocatalysts is one of the most promising research areas for many applications. In this work, the synthesized nanocomposite combines several advantages such as the photoresponse shift from the UV region toward visible light by narrowing the band gap of the semiconductor, magnetic separation ability and dual applications including the catalytic reduction of p-nitrophenol (PNP) and the photocatalytic degradation of methylene blue (MB) dye. In addition to the core magnetite nanoparticles (NPs), the synthesized nanocomposite contains polypyrrole (PPY) and TiO2 shells that are decorated with silver metal NPs to prevent electron–hole recombination and to enhance the catalytic performance. Indeed, the catalytic PNP reduction experiments reveal that the synthesized nanocomposite exhibits significantly high catalytic activity with a rate constant of 0.1169 min−1. Moreover, the photocatalytic experiments show that the synthesized nanophotocatalyst has a boosting effect toward MB dye degradation under normal daytime visible light irradiation with a rate constant of 6.38 × 10−2 min−1. The synergetic effect between silver NPs, PPY and TiO2 is thought to play a fundamental role in enhancing the photocatalytic activity.

An efficient method to synthesize a magnetic nanocomposite with dual catalytic activities with a synergetic effect between Ag nanoparticles, polypyrrole and TiO2 is described.
Keywords:
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号