TAP-2: An interrogative kinetics approach

被引:315
作者
Gleaves, JT [1 ]
Yablonskii, GS [1 ]
Phanawadee, P [1 ]
Schuurman, Y [1 ]
机构
[1] INST RECH CATALYSE, CNRS, F-69626 VILLEURBANNE, FRANCE
基金
美国国家科学基金会;
关键词
kinetics; transient response; high vacuum; selective oxidation; VPO;
D O I
10.1016/S0926-860X(97)00124-5
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The TAP-2 reactor system and the theoretical basis of TAP pulse response experiments are discussed. On the basis of the TAP system, an alternative to the traditional kinetic approach in heterogeneous catalysis is developed. This new approach, termed 'interrogative kinetics' involves a combination of two types of kinetic experiments called 'state-defining' (friendly) and 'state-altering' (typical) experiments. The state defining kinetic parameter, or 'kinetic parameter of the catalyst' (KPC) is proposed and compared with the kinetic characteristic 'turnover number'. The theory of TAP pulse response experiments is developed. Two deterministic models based on partial-differential equations are analyzed for the cases of diffusion, irreversible adsorption/reaction and reversible adsorption. The 'standard diffusion curve' that can be used for distinguishing the Knudsen flow regime is described, and simple criteria of the Knudsen regime are proposed. The concept of relative flow is described, and different fingerprints of TAP kinetics for irreversible adsorption/reaction and reversible adsorption are presented. TAP-2 experimental results on the selective oxidation of n-butane are used to illustrate the methodology of interrogative kinetics.
引用
收藏
页码:55 / 88
页数:34
相关论文
共 34 条
[1]   SELECTIVE OXIDATION OF NORMAL-BUTANE TO MALEIC-ANHYDRIDE .1. OPTIMIZATION STUDIES [J].
BEJ, SK ;
RAO, MS .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1991, 30 (08) :1819-1824
[2]   ROLE OF SURFACE SCIENCE EXPERIMENTS IN UNDERSTANDING HETEROGENEOUS CATALYSIS [J].
BONZEL, HP .
SURFACE SCIENCE, 1977, 68 (01) :236-258
[3]   TURNOVER RATES IN HETEROGENEOUS CATALYSIS [J].
BOUDART, M .
CHEMICAL REVIEWS, 1995, 95 (03) :661-666
[4]   KINETICS AND REDOX PROPERTIES OF VANADIUM PHOSPHATE CATALYSTS FOR BUTANE OXIDATION [J].
BUCHANAN, JS ;
SUNDARESAN, S .
APPLIED CATALYSIS, 1986, 26 (1-2) :211-226
[5]   TRANSIENT STUDIES ON THE ROLE OF OXYGEN ACTIVATION IN THE OXIDATIVE COUPLING OF METHANE OVER SM2O3, SM2O3/MGO, AND MGO CATALYTIC SURFACES [J].
BUYEVSKAYA, OV ;
ROTHAEMEL, M ;
ZANTHOFF, HW ;
BAERNS, M .
JOURNAL OF CATALYSIS, 1994, 150 (01) :71-80
[6]   NATURE OF ACTIVE SPECIES OF (VO)2P2O7 FOR SELECTIVE OXIDATION OF N-BUTANE TO MALEIC-ANHYDRIDE [J].
CENTI, G ;
TRIFIRO, F ;
BUSCA, G ;
EBNER, J ;
GLEAVES, J .
FARADAY DISCUSSIONS, 1989, 87 :215-225
[7]   VANADYL PYROPHOSPHATE - A CRITICAL OVERVIEW [J].
CENTI, G .
CATALYSIS TODAY, 1993, 16 (01) :5-26
[8]   MECHANISTIC ASPECTS OF MALEIC-ANHYDRIDE SYNTHESIS FROM C4-HYDROCARBONS OVER PHOSPHORUS VANADIUM-OXIDE [J].
CENTI, G ;
TRIFIRO, F ;
EBNER, JR ;
FRANCHETTI, VM .
CHEMICAL REVIEWS, 1988, 88 (01) :55-80
[9]   CHROMIUM OXIDE-CATALYZED DISPROPORTIONATION OF CHLORODIFLUOROMETHANE - A MECHANISM STUDY [J].
COULSON, DR ;
WIJNEN, PWJG ;
LEROU, JJ ;
MANZER, LE .
JOURNAL OF CATALYSIS, 1993, 140 (01) :103-120
[10]  
COULSON DR, 1992, STUD SURF SCI CATAL, V72, P305