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Title: Fe{sub 3}O{sub 4}@graphene oxide composite: A magnetically separable and efficient catalyst for the reduction of nitroarenes

Journal Article · · Materials Research Bulletin
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  1. Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology, Changzhou University, Jiangsu Province, Changzhou 213164 (China)
  2. Key Laboratory of Ministry of Education for Soft Chemistry and Functional Materials, Nanjing University of Science and Technology, Nanjing 210094 (China)

Highlights: ► The Fe{sub 3}O{sub 4}@GO composite was prepared by a facile co-precipitation method. ► Fe{sub 3}O{sub 4} nanoparticles are well distributed on GO nanosheets. ► Fe{sub 3}O{sub 4}@GO was for the first time explored as a catalyst to reduce nitroarenes. ► Fe{sub 3}O{sub 4}@GO exhibits higher catalytic activity. ► The composite catalyst is easily recycled due to its magnetic separability. - Abstract: We reported a facile co-precipitation method to prepare a highly active Fe{sub 3}O{sub 4}@graphene oxide (Fe{sub 3}O{sub 4}@GO) composite catalyst, which was fully characterized by means of X-ray diffraction (XRD), Fourier transformed infrared (FTIR) spectroscopy, transmission electron microscopy (TEM) and N{sub 2} adsorption–desorption measurements. The results demonstrated that the Fe{sub 3}O{sub 4} nanoparticles (Fe{sub 3}O{sub 4} NPs) with a small diameter of around 12 nm were densely and evenly deposited on the graphene oxide (GO) sheets. The as-prepared Fe{sub 3}O{sub 4}@GO composite was explored as a catalyst to reduce a series of nitroarenes for the first time, which exhibited a great activity with a turnover frequency (TOF) of 3.63 min{sup −1}, forty five times that of the commercial Fe{sub 3}O{sub 4} NPs. The dosages of catalyst and hydrazine hydrate are both less than those reported. Furthermore, the composite catalyst can be easily recovered due to its magnetic separability and high stability.

OSTI ID:
22290432
Journal Information:
Materials Research Bulletin, Vol. 48, Issue 5; Other Information: Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA); ISSN 0025-5408
Country of Publication:
United States
Language:
English