首页> 外文会议>International Conference on Carbon Dioxide Utilization; 20050620-23; Oslo(NO) >Performance of catalytic reactors for the hydrogenation of CO_2 to hydrocarbons
【24h】

Performance of catalytic reactors for the hydrogenation of CO_2 to hydrocarbons

机译:催化反应器将CO_2加氢成烃的性能

获取原文
获取原文并翻译 | 示例

摘要

Fluidized bed and slurry reactors were employed to increase the CO_2 conversion and desirable product selectivity in the direct hydrogenation of CO_2 to hydrocarbons over K-promoted iron catalysts, as it is beneficial for the removal of heat generated due to highly exothermic nature of the reaction. The iron catalysts (Fe-K/Al_2O_3 and Fe-Cu-Al-K) were characterized by BET surface area, CO_2 and H_2 chemisorption, temperature-programmed reduction (TPR), X-ray diffraction (XRD) and temperature-programmed hydrogenation (TPH) The results of TPR and TPH study clearly indicated that co-precipitated Fe-Cu-Al-K catalyst has much higher reducibility and catalytic activity of CO_2 hydrogenation at low temperature than Fe-K/Al_2O_3. The performance of fluidized bed or slurry reactors was superior to that of fixed bed reactor for the CO_2 hydrogenation over Fe-Cu-Al-K catalyst in terms of CO_2 conversion and hydrocarbon productivity. Moreover, light olefins and heavy hydrocarbons were selectively synthesized in fluidized bed and slurry reactors, respectively. The optimum operation conditions and the effects of operating variables on the CO_2 conversion and its product distribution in these catalytic reactors were also discussed.
机译:在通过K促进的铁催化剂将CO_2直接加氢成烃的过程中,采用流化床和淤浆反应器来提高CO_2的转化率和所需的产物选择性,因为这有利于除去由于反应的高放热性质而产生的热量。铁催化剂(Fe-K / Al_2O_3和Fe-Cu-Al-K)的特征在于BET表面积,CO_2和H_2的化学吸附,程序升温还原(TPR),X射线衍射(XRD)和程序升温加氢(TPH)TPR和TPH研究结果清楚地表明,与Fe-K / Al_2O_3相比,共沉淀Fe-Cu-Al-K催化剂在低温下具有更强的还原性和CO_2加氢的催化活性。就CO_2转化率和烃产率而言,与Fe-Cu-Al-K催化剂相比,流化床或淤浆反应器的性能优于Fe-Cu-Al-K催化剂的固定床反应器。此外,分别在流化床和淤浆反应器中选择性地合成了轻质烯烃和重质烃。还讨论了在这些催化反应器中的最佳操作条件和操作变量对CO_2转化及其产物分布的影响。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号