The Role of Support in Formic Acid Decomposition on Gold Catalysts
Formic acid (FA) can easily be decomposed, affording molecular hydrogen through a controllable catalytic process, thus attaining great importance as a convenient hydrogen carrier for hydrogen energetics. Supported gold nanoparticles are considered to be among the most promising catalysts for such ap...
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Online Access: | https://www.mdpi.com/1996-1073/12/21/4198 |
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doaj-085c885122784a3c8d9a272ab29e15d82020-11-25T02:35:54ZengMDPI AGEnergies1996-10732019-11-011221419810.3390/en12214198en12214198The Role of Support in Formic Acid Decomposition on Gold CatalystsVladimir Sobolev0Igor Asanov1Konstantin Koltunov2Boreskov Institute of Catalysis SB RAS, 630090 Novosibirsk, RussiaNikolaev Institute of Inorganic Chemistry SB RAS, 630090 Novosibirsk, RussiaBoreskov Institute of Catalysis SB RAS, 630090 Novosibirsk, RussiaFormic acid (FA) can easily be decomposed, affording molecular hydrogen through a controllable catalytic process, thus attaining great importance as a convenient hydrogen carrier for hydrogen energetics. Supported gold nanoparticles are considered to be among the most promising catalysts for such applications. However, questions remain regarding the influence of the catalyst support on the reaction selectivity. In this study, we have examined the catalytic activity of typical gold catalysts, such as Au/TiO<sub>2</sub>, Au/SiO<sub>2,</sub> and Au/Al<sub>2</sub>O<sub>3</sub> in decomposition of FA, and then compared it with the catalytic activity of corresponding supports. The performance of each catalyst and support was evaluated using a gas-flow packed-bed reactor. It is shown that the target reaction, FA → H<sub>2</sub> + CO<sub>2</sub>, is provided by the presence of gold nanoparticles, whereas the concurrent, undesirable pathway, such as FA → H<sub>2</sub>O + CO, results exclusively from the acid-base behavior of supports.https://www.mdpi.com/1996-1073/12/21/4198hydrogen energeticshydrogen carrierformic acid dehydrogenationsupported gold catalysts |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Vladimir Sobolev Igor Asanov Konstantin Koltunov |
spellingShingle |
Vladimir Sobolev Igor Asanov Konstantin Koltunov The Role of Support in Formic Acid Decomposition on Gold Catalysts Energies hydrogen energetics hydrogen carrier formic acid dehydrogenation supported gold catalysts |
author_facet |
Vladimir Sobolev Igor Asanov Konstantin Koltunov |
author_sort |
Vladimir Sobolev |
title |
The Role of Support in Formic Acid Decomposition on Gold Catalysts |
title_short |
The Role of Support in Formic Acid Decomposition on Gold Catalysts |
title_full |
The Role of Support in Formic Acid Decomposition on Gold Catalysts |
title_fullStr |
The Role of Support in Formic Acid Decomposition on Gold Catalysts |
title_full_unstemmed |
The Role of Support in Formic Acid Decomposition on Gold Catalysts |
title_sort |
role of support in formic acid decomposition on gold catalysts |
publisher |
MDPI AG |
series |
Energies |
issn |
1996-1073 |
publishDate |
2019-11-01 |
description |
Formic acid (FA) can easily be decomposed, affording molecular hydrogen through a controllable catalytic process, thus attaining great importance as a convenient hydrogen carrier for hydrogen energetics. Supported gold nanoparticles are considered to be among the most promising catalysts for such applications. However, questions remain regarding the influence of the catalyst support on the reaction selectivity. In this study, we have examined the catalytic activity of typical gold catalysts, such as Au/TiO<sub>2</sub>, Au/SiO<sub>2,</sub> and Au/Al<sub>2</sub>O<sub>3</sub> in decomposition of FA, and then compared it with the catalytic activity of corresponding supports. The performance of each catalyst and support was evaluated using a gas-flow packed-bed reactor. It is shown that the target reaction, FA → H<sub>2</sub> + CO<sub>2</sub>, is provided by the presence of gold nanoparticles, whereas the concurrent, undesirable pathway, such as FA → H<sub>2</sub>O + CO, results exclusively from the acid-base behavior of supports. |
topic |
hydrogen energetics hydrogen carrier formic acid dehydrogenation supported gold catalysts |
url |
https://www.mdpi.com/1996-1073/12/21/4198 |
work_keys_str_mv |
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