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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Main Authors: Vladimir Sobolev, Igor Asanov, Konstantin Koltunov
Format: Article
Language:English
Published: MDPI AG 2019-11-01
Series:Energies
Subjects:
Online Access:https://www.mdpi.com/1996-1073/12/21/4198
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spelling 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 &#8594; H<sub>2</sub> + CO<sub>2</sub>, is provided by the presence of gold nanoparticles, whereas the concurrent, undesirable pathway, such as FA &#8594; 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 &#8594; H<sub>2</sub> + CO<sub>2</sub>, is provided by the presence of gold nanoparticles, whereas the concurrent, undesirable pathway, such as FA &#8594; 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
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