首页 | 本学科首页   官方微博 | 高级检索  
     检索      

Co/SiO2催化剂合成重质烃的反应性能
引用本文:高海燕,陈建刚,相宏伟,杨继礼,李永旺,孙予罕.Co/SiO2催化剂合成重质烃的反应性能[J].催化学报,2001,22(2):133-137.
作者姓名:高海燕  陈建刚  相宏伟  杨继礼  李永旺  孙予罕
作者单位:中国科学院山西煤炭化学研究所煤转化国家重点实验室, 太原 030001
基金项目:国家重点基础研究发展计划(973计划)
摘    要: 对近期筛选出的一种重质烃合成反应性能良好的Co/SiO2催化剂进行了500h的寿命试验,考察了在不同反应温度、压力和空速条件下催化剂的反应性能.结果表明,随着反应的进行,催化剂合成重质烃的选择性基本保持不变,但催化剂的活性缓慢下降;经原位再生后,催化剂活性可基本恢复到原来的水平.烃产物主要由烷烃组成,C5+中烯烃仅占2.25%,产物主要集中在C12~C20馏分段,水相产物中含3.56%~6.56%的有机含氧化合物,其中主要是低碳醇.

关 键 词:费-托合成  钴基催化剂  重质烃
收稿时间:2001-04-25

Performance of Co/SiO2 Catalyst for the Synthesis of Heavy Hydrocarbons in F-T Reaction
GAO Haiyan,CHEN Jiangang,XIANG Hongwei ,YANG Jili,LI Yongwang,SUN Yuhan.Performance of Co/SiO2 Catalyst for the Synthesis of Heavy Hydrocarbons in F-T Reaction[J].Chinese Journal of Catalysis,2001,22(2):133-137.
Authors:GAO Haiyan  CHEN Jiangang  XIANG Hongwei  YANG Jili  LI Yongwang  SUN Yuhan
Institution:GAO Haiyan,CHEN Jiangang,XIANG Hongwei *,YANG Jili,LI Yongwang,SUN Yuhan
Abstract:A Co/SiO2 catalyst is prepared and used in F-T reaction for thesynthesis of heavy hydrocarbons. The effects of various operation conditions including temper ature, pressure and space velocity on its performance are investigated and a tes t for the catalyst stability is carried out for 500 h. The experimental results show that the C5+ selectivity has only a little change on stream, but CO conversion gradually decreases. Thus the reaction temperature must be raised slow ly to maintain the catalyst activity. After H2 regeneration in situ, the a ctivity is approximately recovered to the original level. Hydrocarbon products are mainly composed of alkane and the content of alkene in C5+ hydrocarbons is about 2.25%. C12~C20 distillate range is superior in hydrocar bon products. The products in water phase contain 3.56%~6.56% of oxygenates w hich are mainly lower carbon number alcohols.
Keywords:Fischer  Tropsch synthesis  cobalt  based catalyst  heavy hydrocarbon
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《催化学报》浏览原始摘要信息
点击此处可从《催化学报》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号