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

Kód výsledku v 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>

Výsledek na webu

<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>

Jazyk výsledku

angličtina

Název v původním jazyce

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

Popis výsledku v původním jazyce

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.

Název v anglickém jazyce

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

Popis výsledku anglicky

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.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

10402 - Inorganic and nuclear chemistry

Projekt

<a href="/cs/project/EF18_046%2F0015974" target="_blank" >EF18_046/0015974: Modernizace České infrastruktury pro integrativní strukturní biologii</a><br>

Návaznosti

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

Rok uplatnění

2025

Kód důvěrnosti údajů

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

Název periodika

Materials Today Chemistry

ISSN

2468-5194

e-ISSN

2468-5194

Svazek periodika

49

Číslo periodika v rámci svazku

OCT

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

11

Strana od-do

1-11

Kód UT WoS článku

001571771100002

EID výsledku v databázi Scopus

2-s2.0-105015531713