The emission of nitrogen oxides NO x into the atmosphere is now 30 million tons annually. Most of these emissions are man-made. The content of N 2 O in the atmosphere is now 0.6 mg/m 3 , which is one or two orders of magnitude greater than the concentration of NO and NO 2 . The annual increment is on the order of 0.2-0.3%. Thus, elucidation of the conditions of the combined catalytic reduction of NO and N 2 O to molecular nitrogen, including selective reduction in the presence of oxygen is an important precursor for protection of the atmosphere [1]. We have already determined the conditions for increasing the conversion of N 2 O in the presence of NO and SO 2 on iron zeolite catalysts [2] and shown that higher NO conversions are achieved on cobalt zeolite (H-ZMS-5) catalysts, while higher N 2 O conversions are achieved on iron zeolite catalysts in the combined reduction of NO and N 2 O by C 3 -C 4 alkanes [3].In the present work, we present the results of a study of the combined reduction of NO and N 2 O by a propane-butane mixture and methane on iron and cobalt catalysts derived from H-ZSM-5 zeolite, zirconium dioxide, and a binary support (H-ZSM-5 + ZrO 2 ) as well as binary (Fe + Co) compositions.The hydrogen form of zeolite ZSM-5 (SiO 2 /Al 2 O 3 = 37) was obtained by ion exchange from an aqueous solution of NH 4 Cl. Iron and cobalt were introduced into the zeolite system by impregnation from solutions of Fe(NO 3 ) 2 ·6H 2 O and Co(NO 3 ) 2 with subsequent drying and roasting at 350°C for 4 h. The preparation of the samples on ZrO 2 and the binary zeolite + zirconium dioxide support was described in our previous work [4]. The catalysts contained 10 mass % Fe x O y and 5 or 10 mass % Co x O y (relative to the metal).The catalytic activity of the samples was characterized by the conversion of N 2 O and NO into nitrogen and was determined in a flow system with a diaphragmless quartz reactor at atmospheric pressure at 250-550°C. The following reaction 386 0040-5760/09/4506-0386