Rapid kinetic measurements in ammonia and methanol syntheses

被引:24
作者
Bielawa, H [1 ]
Kurtz, M [1 ]
Genger, T [1 ]
Hinrichsen, O [1 ]
机构
[1] Ruhr Univ Bochum, Lab Ind Chem, D-44780 Bochum, Germany
关键词
D O I
10.1021/ie0008225
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Kinetic measurements in heterogeneous catalysis are essential for the derivation of rate expressions that are necessary for the design of reactors and that can serve for data extrapolation beyond the measured data range. To accelerate the acquisition of kinetic data, the method of quasi-isothermal temperature-programming has been applied to a study of the kinetics of the ammonia and methanol syntheses. Both reactions were performed in a microcatalytic reactor setup near industrial reaction conditions. For the ammonia synthesis, the technique turned out to be a useful screening method for Ru-based catalysts, which allowed power-law rate expressions to be derived rapidly. Moreover, the in situ temperature-programmed surface reaction of N-* with gas-phase H-2 (N-* TPSR) was studied in detail, allowing for its application as a fast method for catalyst screening within the class of unpromoted Ru-based catalysts. However, in the methanol synthesis, the applicability of the quasi-isothermal temperature-programmed method is limited to qualitative catalyst screening because of the methanol adsorbing capacity and the slow change of the state of the working Cu/ZnO/Al2O3 catalyst.
引用
收藏
页码:2793 / 2800
页数:8
相关论文
共 44 条
[21]   The microkinetics of ammonia synthesis catalyzed by cesium-promoted supported ruthenium [J].
Hinrichsen, O ;
Rosowski, F ;
Muhler, M ;
Ertl, G .
CHEMICAL ENGINEERING SCIENCE, 1996, 51 (10) :1683-1690
[22]  
Hinrichsen O, 1997, STUD SURF SCI CATAL, V109, P389
[23]  
Hinrichsen O, 1999, CHEM ENG TECHNOL, V22, P1039, DOI 10.1002/(SICI)1521-4125(199912)22:12<1039::AID-CEAT1039>3.0.CO
[24]  
2-5
[25]   The kinetics of ammonia synthesis over Ru-based catalysts .1. The dissociative chemisorption and associative desorption of N-2 [J].
Hinrichsen, O ;
Rosowski, F ;
Hornung, A ;
Muhler, M ;
Ertl, G .
JOURNAL OF CATALYSIS, 1997, 165 (01) :33-44
[26]  
Jandeleit B, 1999, ANGEW CHEM INT EDIT, V38, P2495
[27]  
JANDELEIT WH, 1999, ANGEW CHEM, V111, P2648
[28]   A COMPARATIVE-STUDY OF METHANOL SYNTHESIS FROM CO2/H-2 AND CO/H-2 OVER A CU/ZNO/AL2O3 CATALYST [J].
LEE, JS ;
LEE, KH ;
LEE, SY ;
KIM, YG .
JOURNAL OF CATALYSIS, 1993, 144 (02) :414-424
[29]   New insights into methanol synthesis catalysts from X-ray absorption spectroscopy [J].
Meitzner, G ;
Iglesia, E .
CATALYSIS TODAY, 1999, 53 (03) :433-441
[30]   EARLY STUDIES OF MULTICOMPONENT CATALYSTS [J].
MITTASCH, A .
ADVANCES IN CATALYSIS, 1950, 2 :81-104