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    Y-Zr-O solid solution supported Ni-based catalysts for hydrogen production via auto-thermal reforming of acetic acid

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    Type
    Article
    Authors
    Hu, Xiaomin cc
    Yang, Jilong
    Sun, Wenjing cc
    Wang, Ning cc
    An, Shuang
    Wang, Qiao
    Zhang, Yu
    Xie, Xingyue
    Huang, Lihong cc
    KAUST Department
    Advanced Membranes and Porous Materials Center, Physical Sciences and Engineering Division, King Abdullah University of Science and Technology, Thuwal 23955-6900, Saudi Arabia
    Date
    2020-06-23
    Online Publication Date
    2020-06-23
    Print Publication Date
    2020-12
    Embargo End Date
    2022-07-03
    Submitted Date
    2020-01-15
    Permanent link to this record
    http://hdl.handle.net/10754/664128
    
    Metadata
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    Abstract
    Auto-thermal reforming (ATR) is an effective route to extract hydrogen from both water and acetic acid (HAc) from bio-oil. With addition of oxygen into ATR, the reaction heat can be balanced, but the migration of oxygen for oxidation of carbonous species from HAc is still a concern. Here, we report NiYxZr0.85-xOy (x = 0, 0.05, 0.1, 0.2, 0.4, 0.85) catalysts with Y-Zr-O solid solution as support for hydrogen production via ATR of HAc. The oxygen vacancies provided by Y-Zr-O solid solution are beneficial to activating surface oxygen species and improve oxygen mobility of the nickel catalyst, thus the oxygen transfer from reactant to product CO and CO2 was enhanced. On the other hand, Ni nanoparticles, the active metal, are highly dispersed on the Y-Zr-O solid solution carrier. Consequently, the NiY0.2Zr0.65O1.75 catalyst exhibits the highest activity and enhanced stability: the acetic acid conversion is near 100 % and the yield of hydrogen reaches 3.0 mol-H2/mol-HAc, and no obviously coking is found after the reaction.
    Citation
    Hu, X., Yang, J., Sun, W., Wang, N., An, S., Wang, Q., … Huang, L. (2020). Y-Zr-O solid solution supported Ni-based catalysts for hydrogen production via auto-thermal reforming of acetic acid. Applied Catalysis B: Environmental, 278, 119264. doi:10.1016/j.apcatb.2020.119264
    Sponsors
    This work was financially supported by International Cooperation Program sponsored by Sichuan Science and Technology Program (2019YFH0181), National Natural Science Foundation of China (21276031), Guangdong Natural Science Foundation (2020A1515010490) and Youth Foundation of Science and Technology Department of Yunnan Province (Grant no. 2016FD066). The authors thank the National Supercomputing Center in Shenzhen (Shenzhen Cloud Computing Center) for providing CASTEP code in the Materials Studio 7.0 package.
    Publisher
    Elsevier BV
    Journal
    Applied Catalysis B: Environmental
    DOI
    10.1016/j.apcatb.2020.119264
    Additional Links
    https://linkinghub.elsevier.com/retrieve/pii/S0926337320306792
    ae974a485f413a2113503eed53cd6c53
    10.1016/j.apcatb.2020.119264
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