4.7 Article

ZnAl2O4 as a novel high-surface-area ozonation catalyst: One-step green synthesis, catalytic performance and mechanism

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 260, Issue -, Pages 623-630

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2014.09.034

Keywords

High-surface-area; Porous; Nanocrystalline ZnAl2O4; Catalytic ozonation; Mechanism

Funding

  1. National Natural Science Foundation of China [20903048, 21005031, 21275065]
  2. National Key Technology Research and Development Program [2012BAD32B03-4]
  3. Fundamental Research Funds for the Central Universities [JUSRP21113, JUS-RP51314B, JUDCF13015]
  4. Postgraduate Innovation Project of Jiangsu Province [OCZZ13-0743]
  5. MOE SAFEA [B13025]

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Due to the great importance of high-surface-area metal oxide catalysts in catalytic ozonation, green and facile synthesis of a novel robust ozonation catalyst with high surface area is greatly attractive. In this paper, using inexpensive inorganic salts as starting materials, a high-surface-area (196 m(2)/g) porous nanocrystalline ZnAl2O4 was prepared by a one-step green hydrothermal method without organic template, high temperature treatment and supported substance. ZnAl2O4 was developed as a novel ozonation catalyst with enhanced catalytic activity in removal of phenol with a high concentration (300 mg/L) and the removal rate of phenol reached 73.4% within 60 min. The slight decrease by 5.7% on phenol removal rate after being used 4 times of catalyst illustrated the good reusability of ZnAl2O4 in catalytic ozonation. The positive linear correlation between catalytic activity and the density of surface hydroxyl groups of catalyst was established. Surface hydroxyl groups and chemisorbed water of catalyst acted as catalytic active sites for the generation of hydroxyl radicals. In the presence of catalyst, ozone transformed into high active hydroxyl radicals, leading to the enhanced removal of phenol in bulk solution. Moreover, ZnAl2O4 can be applied in a wide pH range from 3.3 to 9.3 and is a promising ozonation catalyst. (C) 2014 Elsevier B.V. All rights reserved.

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