Bimetallic Co-Re/TiO catalysts were developed for efficient citral hydrogenation. Bimetallic catalysts were prepared by co-impregnation (CI), successive-impregnation (SI), and surface redox method (SR). The arrangement between the Co and Re species on these systems was fully characterized using several techniques (TEM-energy-dispersive X-ray spectroscopy, H temperature-programmed reduction, temperature-programmed desorption, XRD, CO FTIR spectroscopy, model reaction of cyclohexane dehydrogenation), and their catalytic performances were evaluated for the selective hydrogenation of citral towards unsaturated alcohols. The Re and Co species are completely isolated in the CI sample, presenting a very limited Co-Re interaction. In SI samples, the metals coexist in a Janus-type structure with a concentration of Re around Co. Decoration/core-shell structures are observed for SR samples resulting from the redox exchange between the metallic surface of the parent Co/TiO catalyst and the Re species of the modifier precursor salt. The contact degree between the two metals gradually increases as follows: Isolated structure (CI)
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http://dx.doi.org/10.1002/cssc.201802744 DOI Listing Publication Analysis
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Ind Eng Chem Res
January 2025
Department of Chemistry, Physics, and Materials Science, Fayetteville State University, Fayetteville, North Carolina 28301, United States.
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Xi'an Jiaotong University, School of Chemical Engineering and Technology, CHINA.
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FEMTO-ST Institute (UMR CNRS 6174), UBFC/UTBM. Site de Montbéliard, 90010, Belfort, France.
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Seoul National University of Science & Technology, Department of Chemical and Biomolecular Engineering, 232 Gongneung-ro, 01811, Seoul, KOREA, REPUBLIC OF.
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Department of Experimental Research and Guangxi Cancer Molecular Medicine Engineering Research Center and Guangxi Key Laboratory of Basic and Translational Research for Colorectal Cancer, Guangxi Medical University Cancer Hospital, Nanning, China.
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