4.7 Article

Manganese-containing hollow TS-1: Description of the catalytic sites and surface properties for solvent -free oxidation of ethylbenzene

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 313, Issue -, Pages 1382-1395

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2016.11.054

Keywords

Ethylbenzene; Selective aerobic oxidation; MnOx/TS-1; Synergic effect

Funding

  1. Natural Science Foundation of China [21576078]
  2. Scientific Research Fund of Hunan Provincial Education Department [15C0816]
  3. Natural Science Foundation Of Hunan Province [2016112081]
  4. Collaborative Innovation Center of New Chemical Technologies for Environmental Benignity and Efficient Resource Utilization
  5. Opening Fund of Key Laboratory of Chemical Biology and Traditional Chinese Medicine Research (Hunan Normal University)
  6. Ministry of Education

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Hollow MnOx/TS-1 catalyst was prepared by dissolution-recrystallization and impregnation method, and its catalytic activity was evaluated in aerobic oxidation of ethylbenzene under solvent-free conditions. Tetrahedral TO4+ and MnOx species homogeneous dispersed on the hollow TS-1 surface and strong favourable synergic interactions between them occurred, which supported by the Comprehensive analysis of XRD, N-2 physical adsorption, TEM, FTIR, UV-vis, XPS and Raman spectroscopy. The virtue of such synergic effect was reflected in a catalytic efficiency enhancement of valuable ketone and alcohol products (TOF = 137 h(-1)): MnOx/TS-1 catalyst showed about 2.2 times higher activity compared to MnOx/Silicalite-1 references. Furthermore, the Mn species content and calcination temperature of the Mn0x/TS-1 catalyst presented significant effects of lower-nuclearity Mn species on the structural, chemical, and catalytic properties. Based on the theoretical calculations, the reaction mechanism was proposed where the cleavage of the longer methylene C-H bond (1.0935 A) of ethylbenzene and O-O bond (1.5267 A) of alkyl hydroperoxide over the O-Ti-O Mn sites is a key step to yield radical continuously for recycle. (C) 2016 Elsevier B.V. All rights reserved.

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