4.7 Article

Synthesis of Co3O4 macrocubes catalyst using novel chitosan/urea template for hydrogen generation from sodium borohydride

期刊

ENERGY
卷 121, 期 -, 页码 238-245

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.energy.2017.01.027

关键词

Hydrogen generation; Cobalt macrocubes; Chitosan; Urea

资金

  1. National Research Foundation of Korea (NRF) - Ministry of Science, ICT and Future Planning [2014R1A2A2A01004352]
  2. Ministry of Education, Republic of Korea. [2009-0093816]
  3. National Research Foundation of Korea [2014R1A2A2A01004352] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

Co3O4 catalyst with porous macrocubes structure were one pot formulated by hydrothermal treatment of chitosan/urea/Co(NO3)(2).6H(2)O mixtures at 180 degrees C for 8 h and then calcined at different temperatures for 4 h. Chitosan and urea are both compounds containing amino group, which made them different from the previous supporting materials. In this study, chitosan was the major template in the solution and determined the shape of the Co3O4 catalyst while urea played a major support to cobalt (II) nitrate hexahydrate during crystal growth of the catalyst. The prepared materials were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared spectrum (FT-IR), UV vis Absorption Spectrum and BET technique. A remarkably high hydrogen generation rate of 1497.55 mIH2 min(-1) g(cat)(-1) was obtained from the hydrolysis of 2 wt% NaBH4 solution with 0.02 g catalyst at 25 degrees C. The catalytic activity of the as-prepared sample was examined for hydrolysis reaction of sodium borohydride (NaBH4) at different temperatures, catalyst amount and NaBH4 concentration. The results reveal that the average crystallite size, macrocubes thickness, surface properties and catalytic activity of Co3O4 macrocubes could be controlled by varying the mass ratio of chitosa/urea to cobalt concentration. (C) 2017 Elsevier Ltd. All rights reserved.

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