Issue 52, 2015

Micro/nano-structured polyaniline/silver catalyzed borohydride reduction of 4-nitrophenol

Abstract

Micro/nano-structured polyaniline/silver (PANI/Ag) composites have been prepared by simply mixing nitric acid doped polyaniline with silver nitrate. A reducing agent was added to accelerate the reaction process and enhance the conversion rate of silver nitrate. As the support material of silver nanoparticles, nitric acid doped polyaniline was synthesized under turbulent flow and surfactants were adopted to control the morphology and uniformity of the particles. Various analysis techniques were adopted to confirm the composition and structure of the composites, including scanning electron microscopy (SEM), X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared spectrometry (FTIR) and energy dispersive X-ray analysis (EDX). The PANI/Ag particles were used as a catalyst in the borohydride reduction reaction of 4-nitrophenol (4-NP), which was online monitored by UV-vis absorption spectroscopy. Results demonstrated that PANI microspheres loaded with 18.30 wt% of silver showed a comparable catalytic performance, and the apparent rate constant is 0.0256 sāˆ’1. Moreover, the stability and reusability of the catalyst were also investigated. The present work highlights the incorporation of well-dispersed silver nanoparticles with the conductive polyaniline matrix, and the accelerated electron transfer during the catalytic process owing to the high electrical conductivity of the support material.

Graphical abstract: Micro/nano-structured polyaniline/silver catalyzed borohydride reduction of 4-nitrophenol

Supplementary files

Article information

Article type
Paper
Submitted
26 Mar 2015
Accepted
27 Apr 2015
First published
27 Apr 2015

RSC Adv., 2015,5, 41639-41645

Author version available

Micro/nano-structured polyaniline/silver catalyzed borohydride reduction of 4-nitrophenol

B. Ma, M. Wang, D. Tian, Y. Pei and L. Yuan, RSC Adv., 2015, 5, 41639 DOI: 10.1039/C5RA05396J

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