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周桂林

教授    硕士生导师

个人信息 更多+
  • 教师英文名称: Guilin Zhou
  • 教师拼音名称: ZGL
  • 电子邮箱:
  • 入职时间: 2006-07-03
  • 所在单位: 环境与资源学院
  • 学历: 博士研究生毕业
  • 办公地点: 新北区(科创园)
  • 性别: 男
  • 学位: 博士
  • 在职信息: 在岗
  • 主要任职: 催化理论与应用技术重庆高校市级重点实验室主任
  • 其他任职: 九三学社重庆市南岸区委员会副主委

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论文成果

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Effects of structure on the carbon dioxide methanation performance of Co-based catalysts

发布时间:2024-10-10
点击次数:

影响因子:
7.139
DOI码:
10.1016/j.ijhydene.2013.05.130
所属单位:
重庆工商大学
教研室:
化学工程系
发表刊物:
international journal of hydrogen energy
项目来源:
重庆工商大学
关键字:
Ordered mesoporous;Co-based catalyst;Carbon dioxide;Methanation;Catalytic hydrogenation
摘要:
Mesoporous Co/KIT-6 and Co/meso-SiO2 catalysts were prepared via hydrogen reduction and were subsequently used in CO2 catalytic hydrogenation to produce methane. The properties of these catalysts were investigated via low-angle X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET) analysis, and transmission electron microscopy (TEM). The results indicate that the synthesized Co/KIT-6 and Co/meso-SiO2 catalysts have mesoporous structures with well-dispersed Co species, as well as high CO2 catalytic hydrogenation activities. The Co/KIT-6 catalyst has a large specific surface area (368.9 m2 g−1) and a highly ordered bicontinuous mesoporous structure. This catalyst exhibits excellent CO2 catalytic hydrogenation activity and methane product selectivity, which are both higher than those of the Co/meso-SiO2 catalyst at high reaction temperatures. The CO2 conversion and methane selectivity of the Co/KIT-6 catalyst at 280 °C are 48.9% and 100%, respectively. The high dispersion of the Co species and the large specific surface area of the prepared Co-based catalysts contribute to the high catalytic activities. In addition, the highly ordered, bicontinuous, mesoporous structure of the Co/KIT-6 catalyst improves the selectivity for the methane product.
第一作者:
周桂林
合写作者:
吴甜,谢红梅,郑旭煦
论文类型:
源刊论文
通讯作者:
周桂林
论文编号:
UI8ETMSRBTYSITROCBOGJLPWBR4TUPS9
学科门类:
工学
一级学科:
化学工程与技术
文献类型:
Journal Article
卷号:
38
期号:
24
页面范围:
10012–10018
是否译文:
发表时间:
2013-08-01
发布期刊链接:
https://doi.org/10.1016/j.ijhydene.2013.05.130