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      Synthesis of silver-anchored polyaniline–chitosan magnetic nanocomposite: a smart system for catalysis

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          Abstract

          A novel and smart four component system composed of chitosan, polyaniline, magnetite and silver was exploited for catalysis.

          Abstract

          A simple route was employed for the fabrication of a polyaniline (PANI)–chitosan (CS)–magnetite (Fe 3O 4) nanocomposite (PANI–CS–Fe 3O 4) via the in situ polymerization of aniline in the presence of CS using anhydrous iron( iii) chloride as an oxidizing agent. The magnetic character of the nanocomposite results from the presence of iron oxide nanoparticles, which were formed as side products during the synthesis of the PANI–CS nanocomposite. The synthesized PANI–CS–Fe 3O 4 nanocomposite was fully characterized using Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), energy dispersive X-ray (EDX), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and vibrating sample magnetometry (VSM). The reduction of silver nitrate by the synthesized nanocomposite enables the anchoring of silver (Ag) nanoparticles onto its surface. The catalytic properties of the Ag-decorated nanocomposite (Ag@PANI–CS–Fe 3O 4) toward the reduction of 4-nitrophenol was investigated using sodium borohydride as a reducing agent.

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          Magnetic iron oxide nanoparticles: synthesis, stabilization, vectorization, physicochemical characterizations, and biological applications.

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            A Nanoreactor Framework of a Au@SiO2 Yolk/Shell Structure for Catalytic Reduction ofp-Nitrophenol

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              Photochemical green synthesis of calcium-alginate-stabilized Ag and Au nanoparticles and their catalytic application to 4-nitrophenol reduction.

              Silver and gold nanoparticles have been grown on calcium alginate gel beads using a green photochemical approach. The gel served as both a reductant and a stabilizer. The nanoparticles were characterized using UV-visible spectroscopy, X-ray diffraction (XRD), scanning and transmission electron microscopy (SEM and TEM), energy dispersive X-ray (EDS), and selected area electron diffraction (SAED) analyses. The particles are spherical, crystalline, and the size ranges for both Ag and Au nanoparticles are <10 nm. It is noticed from the sorption experiment that the loading of gold on calcium alginate beads is much more compared to that of Ag. The effectiveness of the as-prepared dried alginate-stabilized Ag and Au nanoparticles as a solid phase heterogeneous catalyst has been evaluated, for the first time, on the well-known 4-nitrophenol (4-NP) reduction to 4-aminophenol (4-AP) in the presence of excess borohydride. The reduction was very efficient and followed zero-order kinetics for both Ag and Au nanocomposites. The effects of borohydride, initial 4-NP concentration, and catalyst dose were evaluated. The catalyst efficiency was examined on the basis of turnover frequency (TOF) and recyclability. The catalytic efficiency of alginate-based Ag catalyst was much more compared to that of the Au catalyst. The as-prepared new solid-phase biopolymer-based catalysts are very efficient, stable, easy to prepare, eco-friendly, and cost-effective, and they have the potential for industrial applications.
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                Author and article information

                Contributors
                (View ORCID Profile)
                (View ORCID Profile)
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                Journal
                RSCACL
                RSC Advances
                RSC Adv.
                Royal Society of Chemistry (RSC)
                2046-2069
                2017
                2017
                : 7
                : 30
                : 18553-18560
                Affiliations
                [1 ]Chemistry Department
                [2 ]Faculty of Science
                [3 ]Tanta University
                [4 ]Tanta 31527
                [5 ]Egypt
                [6 ]Department of Physics and Measurements
                [7 ]Faculty of Chemical Engineering
                [8 ]University of Chemistry and Technology
                [9 ]166 28 Prague
                [10 ]Czech Republic
                Article
                10.1039/C7RA02575K
                1f14e9d3-2462-4356-9f7b-6b1ebfa05971
                © 2017
                History

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