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      Electrospun Foamlike NiO/CuO Nanocomposites with Superior Catalytic Activity toward the Reduction of 4-Nitrophenol

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      ACS Omega
      American Chemical Society

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          Abstract

          Foamlike NiO/CuO nanocomposites were prepared using a simple electrospinning technique combined with appropriate calcination. By tuning the Ni/Cu molar ratio (1:2, 1:1, and 2:1) in the initial material, different NiO/CuO nanocomposites were obtained. X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), X-ray photoelectron spectroscopy (XPS), and nitrogen adsorption–desorption isotherms were used to characterize the composites. Furthermore, they were investigated as catalysts for the reduction of 4-nitrophenol (4-NP) in the presence of NaBH 4. The test results demonstrate that the nanocomposite with Ni/Cu = 1:1 presents the best catalytic activity for its high content of surface oxygen vacancy and specific surface area.

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          Most cited references51

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          Kinetic Analysis of Catalytic Reduction of 4-Nitrophenol by Metallic Nanoparticles Immobilized in Spherical Polyelectrolyte Brushes

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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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              Comparison of Nanoscaled and Bulk NiO Structural and Environmental Characteristics by XRD, XAFS, and XPS

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                Author and article information

                Journal
                ACS Omega
                ACS Omega
                ao
                acsodf
                ACS Omega
                American Chemical Society
                2470-1343
                14 May 2020
                26 May 2020
                : 5
                : 20
                : 11324-11332
                Affiliations
                [1]State Key Laboratory of Biobased Material and Green Papermaking, Qilu University of Technology (Shandong Academy of Sciences) , Jinan 250353, P. R. China
                Author notes
                [* ]Email: dingtang0120@ 123456aliyun.com . Tel/Fax: +86-531-89631632.
                Article
                10.1021/acsomega.0c00122
                7254509
                abebd481-27b2-4a39-83bf-c05c53c8e736
                Copyright © 2020 American Chemical Society

                This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes.

                History
                : 10 January 2020
                : 24 April 2020
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                ao0c00122

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