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   <subfield code="a">Photocatalytic Degradation of Ni(II)-Cyano and Co(III)-Cyano Complexes</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Khemarath Osathaphan, Kaiwit Ruengruehan, Ria Yngard, Virender Sharma]</subfield>
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   <subfield code="a">Cyanide and metal-cyanide complexes are common constituents of effluents of mining, petroleum refining, and coal gasification. This paper presents the photocatalytic degradation of free cyanide, Ni(II)-cyanide (Ni(CN)4 2−), and Co(III)-cyanide (Co(CN)6 3−) complexes in aqueous TiO2 suspensions. The effect of pH (9.5-12.0), TiO2 loading (0.1-2.0g/l), and the airflow rate (0.5-2.0l/min) in a photoreactor on the degradation of the cyanide complexes was investigated. Free cyanide fully converted to cyanate (NCO−) under alkaline conditions. The maximum removal of the Ni(CN)4 2− ion in 180min was found to be 90%; forming CN− and NCO− ions as the major and minor products, respectively. Comparatively, the Co(CN)6 3− ion could be degraded only up to 30% in 180min. The schemes of the photocatalytic oxidation of cyanides are briefly described. The possible causes for differences in degradation of Ni(CN)4 2− and Co(CN)6 3− are also discussed. Optimum conditions for efficient removal of Ni(CN)4 2− and Co(CN)6 3− ions separately and in mixtures are given.</subfield>
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