Pr-promoted Ni exsolution from Ni-Mg-Al (O) as catalysts for syngas production by dry reforming of methane

被引:5
|
作者
Ojeda-Nino, Oscar [1 ]
Gallego, Jaime [2 ,3 ]
Daza, Carlos E. [1 ]
机构
[1] Univ Nacl Colombia, Fac Ciencias, Dept Quim, Estado Solid & Catalisis Ambiental, AK 30 45-03, Bogota, Colombia
[2] Justus Liebig Univ, Ctr Mat Res, Henrich Buff Ring 17, D-35392 Giessen, Germany
[3] Justus Liebig Univ, Inst Phys Chem, Heinrich Buff Ring, D-35392 Giessen, Germany
关键词
Mixed oxides; Nickel exsolution; Biogas valorization; Alternative synthesis methodologies; LOW-TEMPERATURE; PARTIAL OXIDATION; SELF-COMBUSTION; CARBON-DIOXIDE; CO2; CE; HYDROTALCITE; PERFORMANCE; NICKEL; CH4;
D O I
10.1016/j.rineng.2022.100821
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
We report the preparation by three methods (coprecipitation, self-combustion, and microwave-assisted self-combustion) of Pr-promoted Ni-catalysts for H-2/CO>1 syngas production by dry reforming of methane (DRM). The catalysts were characterized by a package of techniques to describe their physicochemical properties including several techniques using CO2 as a probe molecule. The catalysts were tested at 600 degrees C (10 h) and 120 L.g(-1) h(-1), without previous H-2-reduction. The coprecipitation method allowed obtaining a catalyst with a higher surface area and CO2 capture capacity (3.1 mg.g(cat)(-1)), a higher number of basic sites, lower average Ni-0 particle size (5.5 nm), higher catalytic conversions (48-65% of CH4 and 39-42% of CO2) and H-2 (H-2/CO = 1.15-1.75) yield but higher C formation. In addition, the catalyst obtained by microwave-assisted self-combustion presented better performance (45-51% of CH4 and 35-38% of CO2) than traditional self-combustion (40-45% of CH4 and 33-35% of CO2). The results showed that not only Ni-0 particle size but also the presence of basic sites with high thermal stability and grain morphology affect the catalytic activity and coke formation.
引用
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页数:10
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