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国家自然科学基金(21161130522)

作品数:4 被引量:35H指数:4
相关作者:张庆红王野邓卫平宋航徐霆更多>>
相关机构:厦门大学更多>>
发文基金:国家自然科学基金国家重点基础研究发展计划国家教育部博士点基金更多>>
相关领域:理学化学工程更多>>

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Recent advances in understanding the key catalyst factors for Fischer-Tropsch synthesis被引量:13
2013年
Catalytic conversion of synthesis gas (CO+H2) into hydrocarbons, also known as Fischer-Tropsch (FT) synthesis, is a crucial reaction for the translbrmation of non-petroleum carbon resources such as coal, natural gas, shale gas, coal-bed gas and biogas, as well as biomass into liquid fuels and chemicals. Many factors can influence the catalytic behavior of a FT catalyst. This review highlights recent advances in understanding some key catalyst factors, including the chemical state of active phases, the promoters, the size and the microenvironment of active phase, which determine the CO conversion activity and the product selectivity, particularly the selectivity to C5 + hydrocarbons.
Qinghong ZhangWeiping DengYe Wang
关键词:MICROENVIRONMENT
Ru particle size effect in Ru/CNT-catalyzed Fischer-Tropsch synthesis被引量:4
2013年
Carbon nanotube (CNT)-supported Ru nanoparticles with mean sizes ranging from 2.3 to 9.2 nm were prepared by different post-treatments and studied for Fischer-Tropsch (FT) synthesis. The effects of Ru particle size on catalytic behaviors were investigated at both shorter and longer contact times. At shorter contact time, where the secondary reactions were insignificant, the turnover frequency (TOF) for CO conversion was dependent on the mean size of Ru particles; TOF increased with the mean size of Ru particles from 2.3 to 6.3 nm and then decreased slightly. At the same time, the selectivities to C5+ hydrocarbons increased gradually with the mean size of Ru particles up to 6.3 nm and then kept almost unchanged with a further increase in Ru particle size. At longer contact time, C10-C20 selectivity increased significantly at the expense of C21+ selectivity, suggesting the occurrence of the selective hydrocracking of C21+ to C10-C20 hydrocarbons.
Jincan KangWeiping DengQinghong ZhangYe Wang
非负载型铁催化剂上二氧化碳加氢制低碳烯烃(英文)被引量:12
2013年
研究了非负载型铁催化剂上CO2加氢制低碳烯烃反应.结果显示,添加碱金属可显著提高铁催化剂上的CO2转化率和烯烃选择性.在经K和Rb修饰的Fe催化剂上,CO2转化率可达约40%,烯烃选择性达到50%以上,其中C2~C4烯烃收率超过10%.催化剂表征结果表明,碱金属促进了催化剂中碳化铁的生成,这可能是催化剂性能提高的一个关键原因.随着K含量由1wt%增加至5wt%,CO2转化率及烯烃选择性均升高.但K含量过高时,催化剂活性降低.这可能是由于催化剂比表面积和CO2化学吸附量降低所致.当K含量为5%~10%时,K-Fe催化剂上烯烃收率较高;进一步添加适量的硼可进一步提高烯烃选择性,且CO2转化率下降不大.
游震亚邓卫平张庆红王野
关键词:二氧化碳加氢反应低碳烯烃铁催化剂
改性H-ZSM-34上氯甲烷催化转化制低碳烯烃(英文)被引量:6
2013年
比较了几种典型的沸石分子筛在氯甲烷转化制乙烯、丙烯和丁烯等低碳烯烃反应中的催化性能,发现H-ZSM-34具有较佳的催化活性和选择性.经乙二胺四乙酸二钠(Na2H2EDTA)水溶液处理,并经离子交换及焙烧后,H-ZSM-34上氯甲烷转化制低碳烯烃的催化性能显著改善.当Na2H2EDTA浓度为0.1 mol/L,反应温度为673 K,CH3Cl分压9.2 kPa时,C2–C4烯烃选择性和收率分别达82%和61%.研究还发现,Ce修饰H-ZSM-34催化剂同样可改善氯甲烷制低碳烯烃的选择性和收率.表征结果表明,Na2H2EDTA处理和Ce修饰均降低了H-ZSM-34的酸性.酸性的降低可抑制低碳烯烃的氢转移反应,继而避免了其进一步转化为低碳烷烃.
徐霆宋航邓卫平张庆红王野
关键词:氯甲烷低碳烯烃酸性
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