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Reduction of carbon dioxide with hydrogen on a CuO–ZnO mixed catalyst under supercritical conditions

Viktor Ignat'evich Bogdan 1, 2
Viktor Ignat'evich Bogdan
, 
Leonid Modestovich Kustov 1, 2
Leonid Modestovich Kustov
10.1016/j.mencom.2015.11.016
Published 2015-11-09
Communication , Volume 25, Issue 6, 446-448
19
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Bogdan V. I., Kustov L. M. Reduction of carbon dioxide with hydrogen on a CuO–ZnO mixed catalyst under supercritical conditions // Mendeleev Communications. 2015. Vol. 25. No. 6. pp. 446-448.
GOST all authors (up to 50) Copy
Bogdan V. I., Kustov L. M. Reduction of carbon dioxide with hydrogen on a CuO–ZnO mixed catalyst under supercritical conditions // Mendeleev Communications. 2015. Vol. 25. No. 6. pp. 446-448.
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TY - JOUR
DO - 10.1016/j.mencom.2015.11.016
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.11.016
TI - Reduction of carbon dioxide with hydrogen on a CuO–ZnO mixed catalyst under supercritical conditions
T2 - Mendeleev Communications
AU - Bogdan, Viktor Ignat'evich
AU - Kustov, Leonid Modestovich
PY - 2015
DA - 2015/11/09
PB - Mendeleev Communications
SP - 446-448
IS - 6
VL - 25
ER -
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@article{2015_Bogdan,
author = {Viktor Ignat'evich Bogdan and Leonid Modestovich Kustov},
title = {Reduction of carbon dioxide with hydrogen on a CuO–ZnO mixed catalyst under supercritical conditions},
journal = {Mendeleev Communications},
year = {2015},
volume = {25},
publisher = {Mendeleev Communications},
month = {Nov},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.11.016},
number = {6},
pages = {446--448},
doi = {10.1016/j.mencom.2015.11.016}
}
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Bogdan, Viktor Ignat'evich, and Leonid Modestovich Kustov. “Reduction of carbon dioxide with hydrogen on a CuO–ZnO mixed catalyst under supercritical conditions.” Mendeleev Communications, vol. 25, no. 6, Nov. 2015, pp. 446-448. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2015.11.016.

Abstract

Reduction of CO2 with hydrogen into CO and CH3OH on a conventional CuO–ZnO mixed catalyst of methanol synthesis under supercritical conditions provided comparable selectivities to methanol and CO with a quite good stability of the catalytic activity; no methanation reaction was observed.

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