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Promotional effect of Ti on mesoporous silica-supported Ru catalysts for CO2 methanation

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F25%3A00142963" target="_blank" >RIV/00216224:14310/25:00142963 - isvavai.cz</a>

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/pii/S2468519425005166?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S2468519425005166?via%3Dihub</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.mtchem.2025.103026" target="_blank" >10.1016/j.mtchem.2025.103026</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Promotional effect of Ti on mesoporous silica-supported Ru catalysts for CO2 methanation

  • Original language description

    Understanding the role of metal promoter in CO2 methanation is essential for advancing catalyst design and developing efficient methanation catalysts. Herein, a series of mesoporous Ti-promoted silica materials with different Ti-loadings was synthesized via the aerosol-assisted sol-gel process. These materials possess a spherical morphology with high specific surface area and homogeneous distribution of dispersed Ti species, even at Tiloading as high as 16 mol%, thus allowing to investigate the role of Ti as a promoter in silica-supported Ru CO2 methanation catalysts. Keeping the Ru loading constant, higher Ti loadings (up to 12 mol%) lead to superior catalytic activity in CO2 methanation. At 300 degrees C, the CH4 formation rate of Ru/12 %Ti-SiO2 catalyst (198 mu molCH4gRu - 1s- 1) is 2.3 times higher than that of unpromoted Ru/SiO2 catalyst (88 mu molCH4gRu - 1s- 1). The improved activity correlates well with the smaller crystallite size of RuO2 nanoparticles, which translates to higher Ru dispersion after reductive treatment with H2. Overall, Ti helps stabilize Ru species and impedes crystal growth. With a Ti loading of 12 mol%, the crystallization of small anatase TiO2 is induced after RuO2 impregnation and during subsequent calcination, in turn forming the interfacial contact between Ru and TiO2 after H2 reduction. In-situ DRIFTS suggests that the promotion of CO2 activation and CO adsorption at these interfacial sites is responsible for the enhanced catalytic activity in Ti-promoted Ru-SiO2 methanation catalyst.

  • 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

    10402 - Inorganic and nuclear chemistry

Result continuities

  • Project

    <a href="/en/project/EF18_046%2F0015974" target="_blank" >EF18_046/0015974: Upgrading Czech Infrastructure for Integrative Structural Biology</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2025

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Materials Today Chemistry

  • ISSN

    2468-5194

  • e-ISSN

    2468-5194

  • Volume of the periodical

    49

  • Issue of the periodical within the volume

    OCT

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    11

  • Pages from-to

    1-11

  • UT code for WoS article

    001571771100002

  • EID of the result in the Scopus database

    2-s2.0-105015531713