Application of the TAP-2 reactor and FTIR in elucidating the mechanism of NO2 reduction by propene over an acidic mordenite

被引:26
作者
Gerlach, T [1 ]
Baerns, M [1 ]
机构
[1] Inst Appl Chem Berlin Adlershof, D-12484 Berlin, Germany
关键词
TAP reactor pulse method in vacuo; FTIR; NOx reduction by propene; intermediates of NO2 reduction;
D O I
10.1016/S0009-2509(99)00037-8
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
A vacuum pulse method (Temporal-Analysis-of-Products (TAP) reactor) and in situ FTIR were applied to study the mechanism of the reduction of NO2 to N-2, by C3H6 over an acidic H-mordenite catalyst. An adsorbed nitrile is formed on the catalyst surface presumably via a nitro or nitroso compound of propene. Upon reaction with water the nitrile yields adsorbed ammonium ions. Ammonium ions on the surface form nitrogen upon reaction with NO2 and may therefore be considered as the decisive intermediate of NO2 reduction by propylene over acidic mordenite catalysts. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:4379 / 4384
页数:6
相关论文
共 13 条
[1]   THE ROLE OF NO2 IN THE REDUCTION OF NO BY HYDROCARBON OVER CU-ZRO2 AND CU-ZSM-5 CATALYSTS [J].
BETHKE, KA ;
LI, C ;
KUNG, MC ;
YANG, B ;
KUNG, HH .
CATALYSIS LETTERS, 1995, 31 (2-3) :287-299
[2]   Surface chemistry of V-Sb-oxide in relation to the mechanism of acrylonitrile synthesis from propane .1. Chemisorption and transformation of possible intermediates [J].
Centi, G ;
Marchi, F ;
Perathoner, S .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1996, 92 (24) :5141-5149
[3]   Kinetic and mechanistic study of NOx reduction by NH3 over H-form zeolites .1. Kinetic and mechanistic insights into NO reduction over H-ZSM-5 [J].
Eng, J ;
Bartholomew, CH .
JOURNAL OF CATALYSIS, 1997, 171 (01) :14-26
[4]  
GERLACH T, 1998, IN PRESS J CATALYSIS
[5]   TAP-2: An interrogative kinetics approach [J].
Gleaves, JT ;
Yablonskii, GS ;
Phanawadee, P ;
Schuurman, Y .
APPLIED CATALYSIS A-GENERAL, 1997, 160 (01) :55-88
[6]   FT-IR study of NO+O2 co-adsorption on H-ZSM-5:: re-assignment of the 2133 cm-1 band to NO+ species [J].
Hadjiivanov, K ;
Saussey, J ;
Freysz, JL ;
Lavalley, JC .
CATALYSIS LETTERS, 1998, 52 (1-2) :103-108
[7]   The role of acid sites in cobalt zeolite catalysts for selective catalytic reduction of NOx [J].
Miller, JT ;
Glusker, E ;
Peddi, R ;
Zheng, T ;
Regalbuto, JR .
CATALYSIS LETTERS, 1998, 51 (1-2) :15-22
[8]   Reduction of nitrogen oxides with hydrocarbons catalyzed by bifunctional catalysts [J].
Misono, M ;
Hirao, Y ;
Yokoyama, C .
CATALYSIS TODAY, 1997, 38 (02) :157-162
[9]  
RATSUMA A, 1995, CATAL LETT, V31, P367
[10]   Low-temperature conversion of NOx to N2 by zeolite-fixed ammonium ions [J].
Richter, M ;
Eckelt, R ;
Parlitz, B ;
Fricke, R .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1998, 15 (1-2) :129-146