Poisoning of iron catalyst by COS in syngas for Fischer—Tropsch synthesis

Q4 Chemical Engineering 分子催化 Pub Date : 1994-11-27 DOI:10.1016/0304-5102(94)87035-7
Zhao-Tie Liu, Jing-Lai Zhou, Bi-Jiang Zhang
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引用次数: 35

Abstract

As a part of converting coal to liquid fuels, the poisoning of commercial FeCuK catalyst in Fischer-Tropsch (FT) synthesis by carbonyl sulfide in synthesis gas was tested. Reduced coprecipitated FeCuK catalyst was investigated with synthesis gas containing 73.2, 184, 232.4, and 350.8 mg of sulfur as COS per cubic meter at 524 K under 2.31 MPa, with an hourly space velocity of 1854. The catalyst activity decreased rapidly in the first few hours of poisoning process, and finally decreased linearly with amount of sulfur fed to the catalyst until the relative activity was 0.01 to 0.05. The deactivation rates were different with the content of sulfur in synthesis gas. The selectivity to methane and gaseous C2C4 hydrocarbons increased when the catalyst was poisoned by COS. The weight content of C+5 in product decreased significantly with increasing sulfur fed to catalyst. The water-gas shift reaction in FT synthesis was also discussed in this work.

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费托合成合成气中铁催化剂的COS中毒研究
作为煤制液体燃料的一部分,对合成气中羰基硫化物合成费托合成(FT)过程中商品FeCuK催化剂的中毒进行了测试。以含硫73.2、184、232.4和350.8 mg的合成气为COS / m3,在524 K、2.31 MPa、每小时空速1854的条件下,研究了还原共沉淀FeCuK催化剂。催化剂活性在中毒过程的前几个小时迅速下降,最后随着硫的添加量的增加呈线性下降,直至相对活性为0.01 ~ 0.05。合成气中硫含量不同,其失活速率也不同。当催化剂被COS毒害时,对甲烷和气态C2C4烃的选择性提高。随着催化剂加硫量的增加,产物中C+5的重量含量显著降低。本文还对FT合成中的水气转换反应进行了讨论。
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来源期刊
分子催化
分子催化 Chemical Engineering-Catalysis
CiteScore
1.50
自引率
0.00%
发文量
2959
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Author index Subject index Hydrolysis of sucrose by dealuminated Y-zeolites Synthesis and application of organophilic polystyrene-montmorillonite supported onium salts in organic reactions Effect of the reduction temperature on the selectivity of the high temperature reaction of acetone and hydrogen over alumina and titania supported nickel and cobalt catalysts
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