催化作用
碳纤维
热重分析
镍
解吸
程序升温还原
材料科学
尖晶石
无机化学
差热分析
吸附
分析化学(期刊)
化学
冶金
衍射
物理化学
有机化学
复合材料
物理
光学
复合数
作者
Xianjin Huang,Wen‐Long Mo,Xiaoqiang He,Xing Fan,Feng‐Yun Ma,Dilhumar Tax
出处
期刊:ACS omega
[American Chemical Society]
日期:2021-06-14
卷期号:6 (25): 16381-16390
被引量:53
标识
DOI:10.1021/acsomega.1c00918
摘要
High Resolution Image Download MS PowerPoint Slide Modified Ni-Al 2 O 3 catalysts with Ca, Co, and Ce species as promoters were prepared by the combustion method, and the structure, morphology, reduction characteristic, and CO 2 –CH 4 reforming of the catalysts were discussed by X-ray diffraction (XRD), H 2 -temperature-programmed reduction (H 2 -TPR), energy-dispersive X-ray (EDX) mapping, NH 3 -temperature-programmed desorption (NH 3 -TPD), N 2 adsorption–desorption, thermogravimetric-differential thermal analysis (TG-DTG), and temperature-programmed hydrogenation (TPH) methods. The crystal size of Ni on Ca-Ni-Al 2 O 3 was 16.97 nm, and the active component and additive were distributed well in the catalyst. Co-Ni-Al 2 O 3 presented a surface area of 65.70 m 2 ·g –1 and a pore diameter of 161.60 nm. Ce-Ni-Al 2 O 3 showed relatively stable nickel–aluminum spinel (NiAl 2 O 4 ), which could not be easily reduced to the active component Ni. Evaluation results demonstrated that the performance of the catalysts followed the order Co-Ni-Al 2 O 3 > Ca-Ni-Al 2 O 3 > Ni-Al 2 O 3 > Ce-Ni-Al 2 O 3 . Carbon deposition analysis showed that the carbon resistance of Ca-Ni-Al 2 O 3 was poor and graphitic carbon was generated on the catalyst. However, Ce-Ni-Al 2 O 3 showed less carbon deposition, which might have resulted from the lower activity of the catalyst.
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