Reactor design issues for synthesis-gas fermentations

被引:178
作者
Bredwell, MD [1 ]
Srivastava, P [1 ]
Worden, RM [1 ]
机构
[1] Michigan State Univ, Dept Chem Engn, E Lansing, MI 48824 USA
关键词
D O I
10.1021/bp990108m
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Synthesis gas is readily obtained by gasifying coal, oil, biomass, or waste organics and represents an abundant, potentially inexpensive, feedstock for bioprocessing. The primary components of synthesis gas, carbon monoxide and hydrogen, can be converted into methane, organic acids, and alcohols via anaerobic fermentations. Bioconversion of synthesis gas is an attractive alternative to catalytic processing because the biological catalysts are highly specific and often more tolerant of sulfur contaminants than inorganic catalysts. However, because the aqueous solubilities of carbon monoxide and hydrogen are low, synthesis-gas fermentations are typically limited by the rate of gas-to-liquid mass transfer. Consequently, a major engineering challenge in commercial development of synthesis-gas fermentations is to provide sufficient gas mass transfer in an energy-efficient manner. This paper reviews recent progress in the development of synthesis-gas fermentations, with emphasis on efforts to increase the efficiency of gas mass transfer. Metabolic properties of several microbes able to ferment synthesis gas are described. Results of synthesis-gas fermentations conducted in various bioreactor configurations are summarized. Recent results showing enhancement of synthesis-gas fermentations using microbubble dispersions are presented, and studies of the mass-transfer and coalescence properties of microbubbles are described.
引用
收藏
页码:834 / 844
页数:11
相关论文
共 96 条
  • [1] High-pressure trickle-bed reactors: A review
    AlDahhan, MH
    Larachi, F
    Dudukovic, MP
    Laurent, A
    [J]. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1997, 36 (08) : 3292 - 3314
  • [2] Alonso C, 1997, BIOTECHNOL BIOENG, V54, P583, DOI 10.1002/(SICI)1097-0290(19970620)54:6<583::AID-BIT9>3.0.CO
  • [3] 2-F
  • [4] DESIGN OF GAS-TREATMENT BIOREACTORS
    ANDREWS, GF
    NOAH, KS
    [J]. BIOTECHNOLOGY PROGRESS, 1995, 11 (05) : 498 - 509
  • [5] LASER CAPILLARY SPECTROPHOTOMETRY FOR DROP-SIZE CONCENTRATION MEASUREMENTS
    BAE, JH
    TAVLARIDES, LL
    [J]. AICHE JOURNAL, 1989, 35 (07) : 1073 - 1084
  • [6] BAKKER A, 1994, CHEM ENG RES DES, V72, P573
  • [7] BIOLOGICAL PRODUCTION OF ALCOHOLS FROM COAL THROUGH INDIRECT LIQUEFACTION
    BARIK, S
    PRIETO, S
    HARRISON, SB
    CLAUSEN, EC
    GADDY, JL
    [J]. APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY, 1988, 18 : 363 - 378
  • [8] Barton JW, 1998, J CHEM TECHNOL BIOT, V72, P93, DOI 10.1002/(SICI)1097-4660(199806)72:2<93::AID-JCTB889>3.0.CO
  • [9] 2-R
  • [10] BAUCKHAGE K, 2 INT S APPL LAS AN