引用本文:
黄传敬, 郑小明, 费金华. 甲烷二氧化碳重整制合成气镍-钴双金属催化剂[J]. 应用化学,
2001, 18(9): 741-745.
Citation: HUANG Chuan-Jing, ZHENG Xiao-Ming, FEI Jin-Hua. Reforming of Methane with Carbon Dioxide to Syngas over Ni-Co Bimetallic Catalysts[J]. Chinese Journal of Applied Chemistry, 2001, 18(9): 741-745.
Citation: HUANG Chuan-Jing, ZHENG Xiao-Ming, FEI Jin-Hua. Reforming of Methane with Carbon Dioxide to Syngas over Ni-Co Bimetallic Catalysts[J]. Chinese Journal of Applied Chemistry, 2001, 18(9): 741-745.
甲烷二氧化碳重整制合成气镍-钴双金属催化剂
摘要:
采用微反-色谱、TPO、TPR和CO2-TPD等技术研究了负载型Ni/SiO2、Co/SiO2和Ni-Co/SiO2催化剂对甲烷二氧化碳重整反应的催化活性、抗积炭性能,并对其还原性能和表面吸附性能进行了表征.发现与单金属催化剂相比,Ni-Co/SiO2双金属催化剂有优越的催化活性和抗积炭性能.催化剂表征结果表明,在Ni-Co/SiO2催化剂中Ni促进了Co的还原,Co提高了催化剂对CO2的吸附能力,抑制了低活性积炭物种的生成.
-
关键词:
- 甲烷二氧化碳重整
- / Ni-Co/SiO2双金属催化剂
- / 积炭
English
Reforming of Methane with Carbon Dioxide to Syngas over Ni-Co Bimetallic Catalysts
Abstract:
Reforming of CH4 with CO2 to give syngas over Ni/SiO2, Co/SiO2 and Ni Co/SiO2 catalysts has been studied by activity evaluation using TPO, TPR and CO2-TPD techniques.It is found that the catalysts without pre reduction decreased in their activities following the order of Ni Co/SiO2~Ni/SiO2>>Co/SiO2, and Ni Co/SiO2 was much less sensitive to coking and more stable than Ni/SiO2 catalyst.The CH4 conversion over Ni Co/SiO2 catalyst increased with time in stream during the first 1 h period of reaction and then remained invariable with time in stream for 9 h, while over Ni/SiO2 catalyst the CH4 conversion decreased continuously with reaction time and the reaction had to be stopped because of the reactor becoming completely plugged by carbon deposits after 6 h.In the case of Ni Co/SiO2 catalyst, Ni promoted the reduction of Co species, which was found beneficial to CO2 adsorption and suppression of less active carbon deposition.This is considered to be related to the excellent activity, stability and anti coking property of the bimetallic catalyst.
-
Key words:
- CH4/CO2 reforming to syngas
- / N-Co/SiO2 catalyst
- / carbon deposition
-
-
扫一扫看文章
计量
- PDF下载量: 1
- 文章访问数: 1041
- HTML全文浏览量: 119

下载: