Induction heating catalysis: Carbon dioxide methanation on deactivation-resistant trimetallic PdRe/Ni nanoconjugates with Ni-supports
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989100%3A27710%2F23%3A10253414" target="_blank" >RIV/61989100:27710/23:10253414 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/62690094:18470/23:50020822
Výsledek na webu
<a href="https://www.sciencedirect.com/science/article/pii/S0263876223005828?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S0263876223005828?via%3Dihub</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.cherd.2023.09.017" target="_blank" >10.1016/j.cherd.2023.09.017</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Induction heating catalysis: Carbon dioxide methanation on deactivation-resistant trimetallic PdRe/Ni nanoconjugates with Ni-supports
Popis výsledku v původním jazyce
The objective of the present study was to assess the scalability of the methanation nanocatalysis controlled by induction heating. We constructed a library of Ni-scaffolds supporting nano-Pd/Re blends using a nano-transfer method that we developed previously as a way to generate nanoparticles and decorate with them various carriers effective in environmental green chemistry applications. We compared their reactivity with that of powdered systems. Through testing these catalyst systems in low-temperatureIHC CO2 methanation, we discovered that a high CO2 methanation activity was closely associated with the oxide-passivation of the surface structures. Unexpectedly, a comprehensive XPS analysis of the catalyst materials' surfaces unveiled the presence of carbon deposits in both the original metals and the constructed and reacted catalysts, although this phenomenon did not diminish the catalysts' reactivity. Our research indicates that a new platform is coking resistant, while IHC control allows for 58 celcius reduction in CO2 methanation temperature compared to silica-supported catalysts controlled methanation performed in the preheated gas stream.
Název v anglickém jazyce
Induction heating catalysis: Carbon dioxide methanation on deactivation-resistant trimetallic PdRe/Ni nanoconjugates with Ni-supports
Popis výsledku anglicky
The objective of the present study was to assess the scalability of the methanation nanocatalysis controlled by induction heating. We constructed a library of Ni-scaffolds supporting nano-Pd/Re blends using a nano-transfer method that we developed previously as a way to generate nanoparticles and decorate with them various carriers effective in environmental green chemistry applications. We compared their reactivity with that of powdered systems. Through testing these catalyst systems in low-temperatureIHC CO2 methanation, we discovered that a high CO2 methanation activity was closely associated with the oxide-passivation of the surface structures. Unexpectedly, a comprehensive XPS analysis of the catalyst materials' surfaces unveiled the presence of carbon deposits in both the original metals and the constructed and reacted catalysts, although this phenomenon did not diminish the catalysts' reactivity. Our research indicates that a new platform is coking resistant, while IHC control allows for 58 celcius reduction in CO2 methanation temperature compared to silica-supported catalysts controlled methanation performed in the preheated gas stream.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
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OECD FORD obor
20400 - Chemical engineering
Návaznosti výsledku
Projekt
—
Návaznosti
—
Ostatní
Rok uplatnění
2023
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Chemical Engineering Research and Design
ISSN
0263-8762
e-ISSN
1744-3563
Svazek periodika
199
Číslo periodika v rámci svazku
NOV 2023
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
13
Strana od-do
102-114
Kód UT WoS článku
001087725600001
EID výsledku v databázi Scopus
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