Structure of Mn–Zr mixed oxides catalysts and their catalytic performance in the gas-phase oxidation of chlorocarbons

• Published in: Chemosphere (Oxford) 2007-06, Vol.68 (6), p.1004-1012
• Main Authors: Gutiérrez-Ortiz, Jose I., de Rivas, Beatriz, López-Fonseca, Rubén, Martín, Susana, González-Velasco, Juan R.
• Format: Article
• Language: English
• Subjects: 1,2-Dichloroethane; Applied sciences; Atmospheric pollution; Catalysis; Catalysts: preparations and properties; Catalytic oxidation; Chemistry; Chlorinated VOC; Ethylene Dichlorides - chemistry; Exact sciences and technology; Gases - chemistry; General and physical chemistry; General processes of purification and dust removal; Manganese - chemistry; Manganese–zirconium mixed oxides; Oxides - chemistry; Pollution; Prevention and purification methods; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry; Trichloroethylene; Trichloroethylene - chemistry; Zirconium - chemistry
• ISSN: 0045-6535; 1879-1298
• DOI: 10.1016/j.chemosphere.2007.02.025

The catalytic activity and selectivity of manganese zirconia mixed oxides were evaluated for the oxidation of two common chlorinated pollutants found in waste streams, namely 1,2-dichloroethane (DCE) and trichloroethylene (TCE). Mixed oxides with varying Mn–Zr content were prepared by coprecipitation via nitrates, and subsequent calcination at 600 °C for 4 h in air. These catalysts were characterised by means of several techniques such as atomic emission spectrometry, N 2 adsorption–desorption, powder X-ray diffraction, temperature-programmed desorption of ammonia, pyridine adsorption followed by diffuse reflectance infrared spectroscopy and temperature-programmed reduction with hydrogen. The active catalytic behaviour of Mn–Zr mixed oxides was ascribed to a substantial surface acidity combined with readily accessible active oxygen species. Hence, the mixed oxide with 40 mol% manganese content was found to be an optimum catalyst for the combustion of both chlorocarbons with a T 50 value around 305 and 315 °C for DCE and TCE oxidation, respectively. The major oxidation products were carbon dioxide, hydrogen chloride and chlorine. It was observed that the formation of both CO 2 and Cl 2 was promoted with Mn loading.