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Catalytic Performance of Alumina-Supported Cobalt Carbide Catalysts for Low-Temperature Fischer-Tropsch Synthesis

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F49777513%3A23640%2F22%3A43967410" target="_blank" >RIV/49777513:23640/22:43967410 - isvavai.cz</a>

  • Alternative codes found

    RIV/62243136:_____/22:N0000017

  • Result on the web

    <a href="https://doi.org/10.3390/catal12101222" target="_blank" >https://doi.org/10.3390/catal12101222</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.3390/catal12101222" target="_blank" >10.3390/catal12101222</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Catalytic Performance of Alumina-Supported Cobalt Carbide Catalysts for Low-Temperature Fischer-Tropsch Synthesis

  • Original language description

    The determination of the catalyst&apos;s active phase helps improve the catalytic performance of the Fischer-Tropsch (FT) synthesis. Different phases of cobalt, including cobalt oxide, carbide, and metal, exist during the reaction. The content of each phase can affect the catalytic performance and product distribution. In this study, a series of cobalt carbide catalysts were synthesized by exposure of Co/Al2O3 catalyst to CH4 at different temperatures from 300 degrees C to 800 degrees C. The physicochemical properties of the carbide catalysts (CoCx/Al2O3) were evaluated by different characterization methods. The catalytic performances of the catalysts were investigated in an autoclave reactor to determine the role of cobalt carbides on the CO conversion and product distribution during the reaction. XRD and XPS analysis confirmed the presence of Co2C in the prepared catalysts. The higher carbidation temperature resulted in the decomposition of methane into hydrogen and carbon, and the presence of graphitic carbon was confirmed by XRD, XPS, SEM, and Raman analysis. The Co2C also decomposed to metallic cobalt and carbon, and the content of cobalt carbide decreased at higher carbidation temperatures. Higher content of Co2C resulted in a lower CO conversion and higher selectivity to light alkanes, mainly methane. The higher carbidation temperature resulted in the decomposition of Co2C to metallic cobalt with higher activity in the FT reaction. The CO conversion increased by increasing the carbidation temperature from 300 degrees C to 800 degrees C, due to the higher content of metallic cobalt. In the presence of pure hydrogen, the Co2C could be converted mainly into hexagonal, close-packed (hcp) Co with higher activity for dissociative adsorption of CO, which resulted in higher catalyst activity and selectivity to heavier hydrocarbons.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    20704 - Energy and fuels

Result continuities

  • Project

    <a href="/en/project/LM2018119" target="_blank" >LM2018119: Catalytic processes for efficient utilization of carbonaceous energy raw materials</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2022

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Catalysts

  • ISSN

    2073-4344

  • e-ISSN

    2073-4344

  • Volume of the periodical

    12

  • Issue of the periodical within the volume

    10

  • Country of publishing house

    CH - SWITZERLAND

  • Number of pages

    18

  • Pages from-to

    nestrankovano

  • UT code for WoS article

    000874386200001

  • EID of the result in the Scopus database

    2-s2.0-85140829556