Carbon nanotube-supported Pd–ZnO catalyst for hydrogenation of CO2 to methanol

• Published in: Applied catalysis. B, Environmental Environmental, 2009-05, Vol.88 (3-4), p.315-322
• Main Authors: Liang, Xue-Lian, Dong, Xin, Lin, Guo-Dong, Zhang, Hong-Bin
• Format: Article
• Language: English
• Subjects: Alloys; Carbon dioxide; Carbon nanotubes; Catalysis; Catalysts; Chemistry; CNT-supported Pd–ZnO catalyst; CO2 hydrogenation; Exact sciences and technology; General and physical chemistry; Hydrogen; Methanol synthesis; nanotechnology; Q1; Temperature; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry
• ISSN: 0926-3373; 1873-3883
• DOI: 10.1016/j.apcatb.2008.11.018

A type of Pd–ZnO catalysts supported on multi-walled carbon nanotubes (MWCNTs) were developed, with excellent performance for CO2 hydrogenation to methanol. Under reaction conditions of 3.0MPa and 523K, the observed turnover-frequency of CO2 hydrogenation reached 1.15×10−2s−1 over the 16%Pd0.1Zn1/CNTs(h-type). This value was 1.17 and 1.18 times that (0.98×10−2 and 0.97×10−2s−1) of the 35%Pd0.1Zn1/AC and 20%Pd0.1Zn1/γ-Al2O3 catalysts with the respective optimal Pd0.1Zn1-loading. Using the MWCNTs in place of AC or γ-Al2O3 as the catalyst support displayed little change in the apparent activation energy for the CO2 hydrogenation, but led to an increase of surface concentration of the Pd0-species in the form of PdZn alloys, a kind of catalytically active Pd0-species closely associated with the methanol generation. On the other hand, the MWCNT-supported Pd–ZnO catalyst could reversibly adsorb a greater amount of hydrogen at temperatures ranging from room temperature to 623K. This unique feature would help to generate a micro-environment with higher concentration of active H-adspecies at the surface of the functioning catalyst, thus increasing the rate of surface hydrogenation reactions. In comparison with the “Parallel-type (p-type)” MWCNTs, the “Herringbone-type (h-type)” MWCNTs possess more active surface (with more dangling bonds), and thus, higher capacity for adsorbing H2, which make their promoting action more remarkable.