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Addition of Zeolite ZSM-5 to an Iron-based Fischer-Tropsch Catalyst supported on Activated Carbon: Effect of Reactor Conditions.

机译:将沸石ZSM-5加到活性炭负载的铁基费托催化剂上:反应器条件的影响。

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摘要

An iron-based catalyst containing 6 wt% Mo, 16 wt% Fe, 0.8 wt% Cu, and 0.9 wt% K supported on Norit SX Ultra activated carbon is used as a FTS catalyst. Zeolite ZSM-5 (of medium acidity and Si/Al = 50) is used to check its effect on FT base catalyst to form aromatic compounds and to reduce the size of long-chain hydrocarbons. The influence of ZSM-5 amounts, bed arrangements, and the temperature on the product distribution were investigated.;The performance of ZSM-5 along with the base catalyst was analyzed in two catalyst bed configurations: separate-bed and mixed-bed. Both separate-bed and mixed-bed catalyst arrangements show conversion of alcohols to hydrocarbons and water. The separate-bed arrangement gives higher conversions of CO and H2, and higher yields of liquid hydrocarbons. The decline in FT activity in the mixed bed is probably due to lowering of the alkali content of the iron catalyst because of alkali migration from FT catalyst to ZSM-5, as confirmed by energy-dispersive X-ray spectroscopy of the spent ZSM-5.;Product profiles were analyzed for changing ZSM-5 weight from 50 to 200% of the FTS amount in the separate bed and the mixed bed catalyst arrangements. Oligomerization, aromatization, isomerization, and cracking reactions are enhanced with increasing ZSM-5 weight in both the catalyst arrangements. The base catalyst shows no selectivity towards aromatic compounds, but addition of ZSM-5 in both arrangements forms C7-10 aromatic compounds. Long-chain hydrocarbon molecules (C13+) formed by the base catalyst are effectively cracked, and isomerized on the ZSM-5 catalyst surface in both type of catalyst arrangements.;Product profiles were analyzed for change in the temperature from 280 to 320°C in the base catalyst as well as in the separate-bed catalyst arrangement. Amounts of small-chain hydrocarbons (C1-5) increase with increase in temperature because of higher FTS rates. Liquid hydrocarbon production rate (in both the base catalyst and the separate bed) is increased at 300°C due to increase in FTS rate. Further increase in the temperature causes these rates to drop to give small-chain hydrocarbon (C1-4) species. Aromatic yields are found to reach a maximum at 300°C in the separate bed. The alcohol rate for the base catalyst increases with increase in temperatures probably because of higher FTS rates. 280°C is sufficient to convert all the alcohols formed by the base catalyst in the separate bed.;The base catalyst and ZSM-5 together were tested for 240 h time on stream (TOS) to check the stability of the combination of the catalysts in the separate-bed arrangement. The base catalyst shows stability up to 120 h and slow decline in activity up to 240 h. A progressive loss of the ZSM-5 activity occurred with TOS. Coke deposition on ZSM-5, confirmed by energy-dispersive X-ray spectroscopy, decreases aromatic compound yield, and increases olefin selectivity with time on stream due to reduction in oligomerization reactions.
机译:负载在Norit SX超活性炭上的含6 wt%Mo,16 wt%Fe,0.8 wt%Cu和0.9 wt%K的铁基催化剂用作FTS催化剂。沸石ZSM-5(中等酸度,Si / Al = 50)用于检查其对FT碱催化剂形成芳族化合物的作用并减小长链烃的尺寸。研究了ZSM-5的用量,床的布置和温度对产物分布的影响。在两个催化剂床配置下,分别对ZSM-5和基础催化剂的性能进行了分析:分离床和混合床。分离床和混合床催化剂布置均显示醇转化为烃和水。分离床布置可实现更高的CO和H2转化率,以及更高的液态烃收率。混合床中FT活性的下降可能是由于碱从FT催化剂迁移到ZSM-5引起的铁催化剂碱含量的降低,这是用过的ZSM-5的能量色散X射线光谱法证实的分析产品概况,以使ZSM-5重量在单独的床和混合床催化剂装置中从FTS量的50%变化到200%。在两种催化剂布置中,随着ZSM-5重量的增加,齐聚,芳构化,异构化和裂化反应均得到增强。碱催化剂对芳族化合物没有选择性,但是在两种排列中加入ZSM-5都会形成C7-10芳族化合物。由基础催化剂形成的长链烃分子(C13 +)被有效裂解,并在两种催化剂排列中均在ZSM-5催化剂表面异构化;;分析了产品曲线,分析了温度从280到320°C基础催化剂以及分离床催化剂装置中的催化剂。由于较高的FTS速率,小链碳氢化合物(C1-5)的数量随温度的升高而增加。由于FTS速率的增加,液态烃的生产速率(在碱催化剂和单独的床中)在300℃下都增加了。温度的进一步升高导致这些速率下降,从而得到小链烃(C1-4)物质。发现在单独的床中,芳烃产率在300℃下达到最大值。碱性催化剂的醇速率随温度的升高而增加,这可能是由于较高的FTS速率。 280°C足以将基础催化剂在单独的床中形成的所有醇转化。;基础催化剂和ZSM-5一起进行了240小时在线运行时间(TOS)测试,以检查催化剂组合的稳定性在分开的床安排。碱性催化剂在120小时内显示出稳定性,在240小时内活性下降缓慢。 TOS导致ZSM-5活性逐渐丧失。通过能量色散X射线光谱法证实,焦炭沉积在ZSM-5上,由于低聚反应的减少,随着时间的流逝,芳烃化合物的收率降低,并且烯烃选择性提高。

著录项

  • 作者

    Karre, Avinashkumar V.;

  • 作者单位

    West Virginia University.;

  • 授予单位 West Virginia University.;
  • 学科 Engineering Chemical.;Engineering Petroleum.
  • 学位 M.S.
  • 年度 2011
  • 页码 161 p.
  • 总页数 161
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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