Outperformance of CaO-incorporated alumina-supported Pd catalysts in methanol decomposition

被引:0
作者
Eryildirim, Busra [1 ]
Oktar, Nuray [2 ]
Dogu, Doruk [3 ]
机构
[1] Gazi Univ, Grad Sch Nat & Appl Sci, Dept Chem Engn, Ankara, Turkiye
[2] Gazi Univ, Fac Engn, Dept Chem Engn, Ankara, Turkiye
[3] Atilim Univ, Dept Met & Mat Engn, Ankara, Turkiye
关键词
Hydrogen; Methanol decomposition; Mayenite; Alumina; Calcium oxide addition; Palladium; HYDROGEN-PRODUCTION; MESOPOROUS ALUMINA; DIMETHYL ETHER; CARBON-DIOXIDE; RAMAN; CU; CO; PERFORMANCE; PALLADIUM; MICROWAVE;
D O I
10.1007/s11164-025-05652-y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This study aimed to investigate the impact of CaO incorporation to alumina-supported Pd catalysts on the methanol decomposition reaction. For this purpose, mayenite, alumina and/or calcium oxide-supported Pd catalysts were synthesized. The synthesized catalysts were characterized by XRD, FTIR, Laser Raman spectroscopy, N2 adsorption-desorption, pyridine adsorbed DRIFTS, CO2-TPD, XPS, SEM-EDS, and ICP-OES techniques. Catalytic activity tests were carried out over a 6 h reaction period in the range of 100-400 degrees C. The results of the characterization and activity tests showed that the addition of CaO had significant effects on the physicochemical properties of the catalyst as well as on the catalytic activity. By adding CaO to the alumina support material, the acidity was reduced, thus reducing the selectivity for dimethyl ether (DME) formation, which is significantly high for the 1Pd@Al2O3 catalyst, and increasing the H2 and CO selectivity. The mayenite-supported catalyst (1Pd@SGM), which contains alumina and calcium oxide in its unique crystal structure, showed an excellent catalytic performance close to complete methanol conversion with DME selectivity below 1% at 400 degrees C. In the stability test carried out at 350 degrees C for 6 h with 1Pd@Al2O3, 1Pd@SGM, and 1Pd@48CaO@Al2O3 catalysts used in the temperature scan, it was concluded that all catalysts were stable and 1Pd@SGM catalyst showed higher catalytic activity than the others.
引用
收藏
页码:4149 / 4176
页数:28
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