Temporal analysis of products (TAP)-Recent advances in technology for kinetic analysis of multi-component catalysts

被引:114
作者
Gleaves, John T. [1 ]
Yablonsky, Gregory [1 ,2 ]
Zheng, Xiaolin [1 ]
Fushimi, Rebecca [1 ]
Mills, Patrick L. [3 ]
机构
[1] Washington Univ, Dept Energy Environm & Chem Engn, St Louis, MO 63130 USA
[2] St Louis Univ, Dept Chem, Pk Coll Engn, St Louis, MO 63103 USA
[3] Texas A&M Univ, Frank H Dotterweich Coll Engn, Dept Chem & Nat Gas Engn, Kingsville, TX 78363 USA
关键词
Temporal analysis of products (TAP); Heterogeneous catalysis; Kinetics; Transient methods; Gas-solid reactions; Knudsen diffusion; Time-of-flight mass spectrometer; Atomic beam deposition; Single particle experiments; Pressure gap; TAP-REACTORS THEORY; VANADYL PYROPHOSPHATE CATALYSTS; HIGH-THROUGHPUT EXPERIMENTATION; SELECTIVITY-DIRECTING FACTORS; PHOSPHORUS OXIDE CATALYSTS; N-BUTANE OXIDATION; CO OXIDATION; N2O DECOMPOSITION; (VO)(2)P2O7 CATALYSTS; TRANSIENT KINETICS;
D O I
10.1016/j.molcata.2009.06.017
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
This paper presents an overview of the evolution, advancements, and capabilities of the temporal analysis of products (TAP) reactor system as a unique catalyst characterization tool. The origination of the TAP reactor based on molecular beam scattering experiments is briefly mentioned. The advancement in TAP reactor design from the TAP-1 system to the TAP-3 system is introduced to highlight its relevance as a Valuable tool for elucidating mechanistic and kinetic aspects of adsorption, diffusion. and reaction in gas-solid systems. Since the invention of the TAP reactor system, a series of TAP microreactor configurations has been introduced with different amounts of catalyst packing starting from the one-zone microreactor to the most recent introduction. the single particle microreactor in which a single Pt particle is packed among 100,000 inert quartz particles An advantage to decreasing the catalyst zone inside the microreactor is to eliminate non-uniformity in the active zone while still achieving high conversions (95%). Experimental designs and results coupling the TAP reactor to other experimental Systems Such as a time-of-flight mass spectrometer and atomic beam deposition system is also presented. Key results from recent TAP experiments are presented to show how the TAP reactor is used to answer fundamental questions in catalysis such as bridging the pressure gap between industrial catalysis and Surface science, understanding the surface lifetimes of reactive adspecies in TAP pump-probe experiments, finding kinetic rate constants related to changes in catalyst composition and its performance. (C) 2009 Elsevier B.V. All rights reserved
引用
收藏
页码:108 / 134
页数:27
相关论文
共 167 条
[1]  
[Anonymous], 2008, NIST EPA NIH MASS SP
[2]  
[Anonymous], SURFACE SCI REPT
[3]  
Asscher M., 1988, Atomic and Molecular Beam Methods, V2
[4]   Bridging the pressure and material gap in the catalytic ammonia oxidation: structural and catalytic properties of different platinum catalysts [J].
Baerns, M ;
Imbihl, R ;
Kondratenko, VA ;
Kraehnert, R ;
Offermans, WK ;
van Santen, RA ;
Scheibe, A .
JOURNAL OF CATALYSIS, 2005, 232 (01) :226-238
[5]   Experiments and processes in the transient regime for heterogeneous catalysis [J].
Bennett, CO .
ADVANCES IN CATALYSIS, VOL 44, 1999, 44 :329-416
[6]   A DYNAMIC METHOD FOR STUDY OF HETEROGENEOUS CATALYTIC KINETICS [J].
BENNETT, CO .
AICHE JOURNAL, 1967, 13 (05) :890-&
[7]  
BENNETT CO, 1982, ACS SYM SER, V178, P1
[8]  
BENNETT CO, 2000, ADV CATAL, V44, P329
[9]   Dynamic methods for catalytic kinetics [J].
Berger, Rob J. ;
Kapteijn, Freek ;
Moulijn, Jacob A. ;
Marin, Guy B. ;
De Wilde, Juray ;
Olea, Maria ;
Chen, De ;
Holmen, Anders ;
Lietti, Luca ;
Tronconi, Enrico ;
Schuurman, Yves .
APPLIED CATALYSIS A-GENERAL, 2008, 342 (1-2) :3-28
[10]   ROLE OF SURFACE SCIENCE EXPERIMENTS IN UNDERSTANDING HETEROGENEOUS CATALYSIS [J].
BONZEL, HP .
SURFACE SCIENCE, 1977, 68 (01) :236-258