期刊
CATALYSTS
卷 11, 期 1, 页码 -出版社
MDPI
DOI: 10.3390/catal11010049
关键词
activated carbon; carbon nanotubes; deactivation; decarbonylation; furan; furfural; furfuryl alcohol; glucose; hydroconversion; Pt-catalysts
资金
- Spanish Project - ERDF/Ministry of Science, Innovation and Universities-State Research Agency [RTI 2018-099224-B100]
Glucose-carbon hybrids were synthesized with different carbon materials and used as Pt-supports for furfural hydroconversion in the gas phase. The reaction pathways produced furfuryl alcohol and furane, with the distribution of products depending on the reaction temperature. The catalytic performance of Pt-catalysts supported on glucose-carbon hybrids was better at low temperatures, and no catalyst deactivation was observed after several hours on stream.
Glucose-carbon hybrids were synthetized with different carbon materials, namely carbon nanotubes, reduced graphene oxide, carbon black and activated carbon by a hydrothermal treatment. These carbon hybrids were used as Pt-supports (1 wt.%) for the furfural (FUR) hydroconversion in the gas phase at mild operating conditions (i.e., P = 1 atm and T = 200 degrees C). The physicochemical properties (porosity, surface chemistry, Pt-dispersion, etc.) were analyzed by different techniques. Glucose-carbon hybrids presented apparent surface areas between 470-500 m(2) g(-1), a neutral character and a good distribution of small Pt-nanoparticles, some large ones with octahedral geometry being also formed. Catalytic results showed two main reaction pathways: (i) FUR hydrogenation to furfuryl alcohol (FOL), and (ii) decarbonylation to furane (FU). The products distribution depended on the reaction temperature, FOL or FU being mainly produced at low (120-140 degrees C) or high temperatures (170-200 degrees C), respectively. At intermediate temperatures, tetrahydrofurfuryl alcohol was formed by secondary FOL hydrogenation. FUR hydroconversion is a structure-sensitive reaction, rounded-shape Pt-nanoparticles producing FU, while large octahedral Pt-particles favor the formation of FOL. Pt-catalysts supported on glucose-carbon hybrids presented a better catalytic performance at low temperature than the catalyst prepared on reference material, no catalyst deactivation being identified after several hours on stream.
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