Published June 15, 2009 | Version v1
Journal article

Catalytic oxidation of cyanides in an aqueous phase over individual and manganese-modified cobalt oxide systems

  • 1. Department of Physical Chemistry, University of Plovdiv, 24 Tzar Assen St, Plovdiv 4000 (Bulgaria)

Description

The possibility for purification of wastewaters containing free cyanides by applying of a new method based on cyanides catalytic oxidation with air to CO2 and N2 at low temperature and atmospheric pressure was investigated. On this purpose, individual and modified with manganese Co-oxide systems as active phase of environmental catalysts were synthesized. The applied method of synthesis favours the preparation of oxide catalytic systems with high active oxygen content (total-O* and surface-O*s) possessing high mobility, and the metal ions being in a high oxidation state and in an octahedral coordination-factors determining high activity in reactions of complete oxidation. The catalysts employed were characterized by powder X-ray diffraction, Infrared spectroscopy, and chemical analysis. The effect of pH of the medium and catalyst loading on the effectiveness of the cyanide oxidation process, expressed by the degree of conversion (α, %), by the rate constant (k, min-1), and COD was studied. The results obtained reveal that using catalysts investigated a high cyanide removal efficiency could be achieved even in strong alkaline medium. The higher activity of the manganese promoted catalytic sample could be explained on the basis of higher total active oxygen content and its higher mobility both depending on the conditions, under which the synthesis of catalyst is being carried out.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.jhazmat.2008.10.051

Additional details

Identifiers

DOI
10.1016/j.jhazmat.2008.10.051;
PII
S0304-3894(08)01542-2;

Publishing Information

Journal Title
Journal of Hazardous Materials
Journal Volume
165
Journal Issue
1-3
Journal Page Range
p. 690-695
ISSN
0304-3894
CODEN
JHMAD9

Optional Information

Copyright
Copyright (c) 2008 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.