In-situ infrared investigation of m-TiO2/α-Fe2O3 photocatalysts and tracing of intermediates in photocatalytic hydrogenation of CO2 to methanol

2022 ◽  
Vol 56 ◽  
pp. 101864
Author(s):  
Munirathinam Elavarasan ◽  
Willie Yang ◽  
Sethupathi Velmurugan ◽  
Jyy-Ning Chen ◽  
Yi-Ting Chang ◽  
...  
Keyword(s):  
2020 ◽  
Vol 11 (26) ◽  
pp. 6766-6774
Author(s):  
Zheng Wang ◽  
Ziwei Zhao ◽  
Yong Li ◽  
Yanxia Zhong ◽  
Qiuyue Zhang ◽  
...  

A novel robust diphosphine–ruthenium(ii) complex has been developed that can efficiently catalyze both the hydrogenation of CO2 to methanol and its in situ condensation with carboxylic acids to give methyl esters.


Author(s):  
Anastasiya Bavykina ◽  
Irina Yarulina ◽  
Lieven Gevers ◽  
Mohamed Nejib Hedhili ◽  
Xiaohe Miao ◽  
...  

<div> <div> <div> <p>The direct hydrogenation of CO2 to methanol using green hydrogen is regarded as a potential technology to reduce greenhouse gas emissions and the dependence on fossil fuels. For this technology to become feasible, highly selective and productive catalysts that can operate under a wide range of reaction conditions near thermodynamic conversion are required. Here, we demonstrate that indium in close contact with cobalt catalyses the formation of methanol from CO2 with high selectivity (>80%) and productivity (0.86 gCH3OH.gcatalyst-1.h-1) at conversion levels close to thermodynamic equilibrium, even at temperatures as high as 300 °C and at moderate pressures (50 bar). The studied In@Co system, obtained via co- precipitation, undergoes in situ transformation under the reaction conditions to form the active phase. Extensive characterization demonstrates that the active catalyst is composed of a mixed metal carbide (Co3InC0.75), indium oxide (In2O3) and metallic Co. </p> </div> </div> </div>


2019 ◽  
Vol 44 (45) ◽  
pp. 24759-24781 ◽  
Author(s):  
Sara Najari ◽  
Gyula Gróf ◽  
Samrand Saeidi

2018 ◽  
Author(s):  
Anastasiya Bavykina ◽  
Irina Yarulina ◽  
Lieven Gevers ◽  
Mohamed Nejib Hedhili ◽  
Xiaohe Miao ◽  
...  

<div> <div> <div> <p>The direct hydrogenation of CO2 to methanol using green hydrogen is regarded as a potential technology to reduce greenhouse gas emissions and the dependence on fossil fuels. For this technology to become feasible, highly selective and productive catalysts that can operate under a wide range of reaction conditions near thermodynamic conversion are required. Here, we demonstrate that indium in close contact with cobalt catalyses the formation of methanol from CO2 with high selectivity (>80%) and productivity (0.86 gCH3OH.gcatalyst-1.h-1) at conversion levels close to thermodynamic equilibrium, even at temperatures as high as 300 °C and at moderate pressures (50 bar). The studied In@Co system, obtained via co- precipitation, undergoes in situ transformation under the reaction conditions to form the active phase. Extensive characterization demonstrates that the active catalyst is composed of a mixed metal carbide (Co3InC0.75), indium oxide (In2O3) and metallic Co. </p> </div> </div> </div>


Sign in / Sign up

Export Citation Format

Share Document