Development of a fixed-bed continuous-flow high-throughput reactor for long-chain n-alkane hydroconversion

被引:43
作者
Huybrechts, W [1 ]
Mijoin, J [1 ]
Jacobs, PA [1 ]
Martens, JA [1 ]
机构
[1] Katholieke Univ Leuven, Ctr Oppervlaktechem & Katalyse, B-3001 Louvain, Belgium
关键词
high-throughput reactor; multi-capillary chromatography; hydroisomerization; ultrastable Y; n-alkanes;
D O I
10.1016/S0926-860X(02)00536-7
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
A high-throughput vapor-phase catalytic experimentation unit with 15 parallel microreactors and fast, on-line GC product analysis was built. The 15 open tubular microreactors were mounted in a single furnace and fed with a common gas stream. Decane hydroisomerization experiments were conducted on 35 mg quantities of reference platinum-loaded ultrastable Y zeolite particles at 200 degreesC, 4.5 bar, using a hydrogen/hydrocarbon molar ratio of 375/1 and contact times of 100-800 kg s/mol. The microreactor outlets were sampled sequentially. GC analysis of the C-1-C-10 alkane product mixtures was achieved in 3.2 min with a multi-capillary column. The actual gas flow rates and contact times in the individual microreactors were derived from the GC FID signals after dilution of the reaction product stream with a calibrated hydrogen gas flow. The maximum temperature difference among the microreactors, measured in an empty reactor unit was ca. 6degreesC at 200degreesC. The conversion data were in excellent agreement with a kinetic model established for a conventional reactor. Fitting of the kinetic data obtained in the individual microreactors; to the model confirmed the small temperature variations depending on the location of each microreactor in the catalyst furnace. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:1 / 13
页数:13
相关论文
共 37 条
  • [21] MARTENS JA, 1986, APPL CATAL, V20, P239
  • [22] THE POTENTIAL AND LIMITATIONS OF THE NORMAL-DECANE HYDROCONVERSION AS A TEST REACTION FOR CHARACTERIZATION OF THE VOID SPACE OF MOLECULAR-SIEVE ZEOLITES
    MARTENS, JA
    JACOBS, PA
    [J]. ZEOLITES, 1986, 6 (05): : 334 - 348
  • [23] Infrared thermographic screening of combinatorial libraries of heterogeneous catalysts
    Moates, FC
    Somani, M
    Annamalai, J
    Richardson, JT
    Luss, D
    Willson, RC
    [J]. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1996, 35 (12) : 4801 - 4803
  • [24] Orschel M, 1999, ANGEW CHEM INT EDIT, V38, P2791, DOI 10.1002/(SICI)1521-3773(19990917)38:18<2791::AID-ANIE2791>3.3.CO
  • [25] 2-J
  • [26] The six-flow reactor technology -: A review on fast catalyst screening and kinetic studies
    Pérez-Ramírez, J
    Berger, RJ
    Mul, G
    Kapteijn, F
    Moulijn, JA
    [J]. CATALYSIS TODAY, 2000, 60 (1-2) : 93 - 109
  • [27] Combinatorial electrochemistry: A highly parallel, optical screening method for discovery of better electrocatalysts
    Reddington, E
    Sapienza, A
    Gurau, B
    Viswanathan, R
    Sarangapani, S
    Smotkin, ES
    Mallouk, TE
    [J]. SCIENCE, 1998, 280 (5370) : 1735 - 1737
  • [28] Reetz MT, 1998, ANGEW CHEM INT EDIT, V37, P2647, DOI 10.1002/(SICI)1521-3773(19981016)37:19<2647::AID-ANIE2647>3.0.CO
  • [29] 2-I
  • [30] Parallel synthesis and fast screening of heterogeneous catalysts
    Rodemerck, U
    Ignaszewski, P
    Lucas, M
    Claus, P
    Baerns, M
    [J]. TOPICS IN CATALYSIS, 2000, 13 (03) : 249 - 252