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K_2CO_3溶液处理对费托合成熔铁催化剂性能的影响 被引量:1

Effect of K_2CO_3 aqueous solution treatment on fused iron catalysts for Fischer-Tropsch synthesis
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摘要 以高频感应炉制备了熔铁催化剂,并进行了K2CO3溶液处理,采用ICP、XRD和H2-TPR等手段,对费托合成熔铁催化剂的物相与组成进行表征。于固定床积分反应器中进行催化剂的费托合成性能评价,反应条件为220℃-350℃,2.0MPa, V(H2)/V(CO)=2,GHSV=3000h-1。结果表明,由于石墨坩埚的使用,使得感应炉制备的熔铁催化剂中引入了大量的Si和Al元素,这些元素与铁氧化物形成固熔体,造成催化剂难以被还原、表面碱度严重被削弱、产物以低碳烃为主。经K2CO3溶液处理后,催化剂中固熔体部分被溶解,还原难度逐步降低。同时,随着K2CO3溶液浓度的增加,催化剂的表面碱度逐渐增强,产物中CH4选择性由44.82%降到28.82%, C2-C4烯烃选择性也逐渐增加。 Fused iron catalysts for Fischer-Tropsch synthesis (FTS)were prepared by induction furnace and then treated with K2CO3 aqueous solution. ICP, XRD and H2-TPR were used to the catalysts, and the FTS performances of the catalysts were investigated in a fixed-bed reactor under the conditions of 220 ℃-350 ℃, 2.0 MPa, H2/CO mole ratio of 2, GHSV of 3000h-1. The results showed that Al and Si introduced from graphite crucible reacted with iron oxide to form solid solution, which severely suppressed the reduction and surface basicity of catalysts and brought high C2-C4 selectivity in FTS. After treatment with K2CO3 aqueous solution, the solid solution was partly dissolved and the extent of reduction gradually increased. As the concentration of K2CO3 aqueous solution increased, surface basicity of catalysts enhanced, which made CH4 selectivity decreased from 44.82% to 28.82%and C2-C4 olefins selectivity improved.
出处 《天然气化工—C1化学与化工》 CAS CSCD 北大核心 2014年第3期48-52,共5页 Natural Gas Chemical Industry
基金 国家自然科学基金资助项目(21373254) 武汉凯迪工程技术研究总院有限公司资助项目(2013WT101) 煤转化国家重点实验室自主研究课题资助项目(2013BWZ004)
关键词 费托合成 熔铁催化剂 感应炉 固熔体 碳酸钾溶液 Fischer-Tropsch synthesis fused iron catalyst induction furnace solid solution potassium carbonate solution
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  • 1Dry M E. Present and future applicatlons of the FlscherTropsch process [J]. Appl Catal A: Gen, 2004, 276(1-2): 1-3. 被引量:1
  • 2Dry M E. The Flscher - Tropsch process: 1950-2000[J]. Catal Today, 2002, 71(3): 227-241. 被引量:1
  • 3Steynberg A P, EspInoza R L, Jager B, et al. Hlgh temperature Flscher - Tropsch synthesls In commerclal practice[J]. Appl Catal A: Cen, 1999, 186(1): 41-54. 被引量:1
  • 4Leckel D. Dlesel productlon from Flscher-Tropsch: The past, the present, and new concepts [J]. Energy Fuels, 2009, 23(5): 2342-2358. 被引量:1
  • 5Zhao R, GoodwIn J G, Jothlmumgesan K, et al. Spraydrled lron Flscher- Tropsch catalysts: Effect of structure on the attrltlon reslstance of the catalysts In the calcIned state[J]. Ind Eng Chem Res, 2001, 40(4): 1065-1075. 被引量:1
  • 6Bukur D B, Lang X, Mukesh D, et al. BInder/support effects on the actlvlty and selectlvlty of lron catalysts In the Flscher- Tropsch synthesls[J].Ind Eng Chem Res,l990, 29(8): 1588-1599. 被引量:1
  • 7Suo H, Wang S, Zhang J, et al. Chemlcal and structural effects of sLIlca In lron-based Flscher- Tropsch synthesls catalysts[J]. J Catal, 2012, 286(1): 111-123. 被引量:1
  • 8Dry M E. The Influence of structural promoters on the surface propertles of reduced magnetlte catalysts [J].J Catal, 1966, 6(2): 194-199. 被引量:1
  • 9Wan H J, WU B S, Zhang C H, et a1. Study on Fe-Al20J Interactlon over preclpltated lron catalyst for FlscherTropsch synthesls[J].Catal Commun,2007 ,8(10): 1538-1545. 被引量:1
  • 10Dry M E, Oosthulzen G I. The correlatlon between catalyst surface abLIlty and hydrocarbon selectlvlty In the FlscherTropsch synthesls[J]. J Catal, 1968, 11(1): 18-24. 被引量:1

二级参考文献111

共引文献139

同被引文献24

  • 1向廷生,蔡春芳,付华娥.不同温度、羧酸溶液中长石溶解模拟实验[J].沉积学报,2004,22(4):597-602. 被引量:52
  • 2徐有生,侯渭,郑海飞,谢鸿森.超临界水的特性及其对地球深部物质研究的意义[J].地球科学进展,1995,10(5):445-449. 被引量:14
  • 3王涵云 杨天宇.原油裂解成气模拟实验.天然气工业,1982,2(3):25-32. 被引量:4
  • 4万俭英,王始波,赵秋枫,汪清源,张世祥.大庆长垣及以西地区泉三、四段扶杨油层储层特征[J].大庆石油地质与开发,2007,26(5):14-17. 被引量:37
  • 5Manning D A C. Gestsdottir K. Feldspar dissolution in the presence of organic acid anions under diagenetic conditions: an experimental study [J] . Organic Geochemistry, 1992, 19 (4) : 483-492. 被引量:1
  • 6Blake I E, Waiter L M. Kinetics of feldspar and quartz dissolution at 70-80% and near-neutral pH: effects of organic acids and NaC1 [J] . Geochimica et Cosmochimica Acta, 1999, 63 (13) : 2043- 2059. 被引量:1
  • 7Butkovskaya N I, Setser D W. Observation of the Unimolecular De- composition Pathways of Chemically Activated Acetic Acid by Fou- rier Transform Infrared Emission Spectrometry [ J ] . J. Phys. Chem, 1995, 99 (28): 11115-11121. 被引量:1
  • 8Michad P, Landoll, Mark T. Holtzapple. Kinetics study of ther- mal decomposition of sodium carboxylate salts [ J] . Biomass and Bioenergy, 2012, 45 (0) : 195-202. 被引量:1
  • 9Osamu Takabashi, Kuniharu Itoh, Ko Saito. A theoretical study of the bifurcation reaction 1I : acetic acid [ J] . Molecular Structure, 2002, 584 ( 1 ) : 249-256. 被引量:1
  • 10Basagiannis A C, Verykios X E. Reforming reactions of acetic acid on nickel catalysts over a wide temperature range [ J ] . Applied Catalysis A: General, 2006, 308 (10) : 182-193. 被引量:1

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