Conversion of CO2 and C2H6 to Propanoic Acid over a Au‐Exchanged MCM‐22 Zeolite. Issue 3 (20th December 2013)
- Record Type:
- Journal Article
- Title:
- Conversion of CO2 and C2H6 to Propanoic Acid over a Au‐Exchanged MCM‐22 Zeolite. Issue 3 (20th December 2013)
- Main Title:
- Conversion of CO2 and C2H6 to Propanoic Acid over a Au‐Exchanged MCM‐22 Zeolite
- Authors:
- Sangthong, Winyoo
Probst, Michael
Limtrakul, Jumras - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Finding novel catalysts for the direct conversion of CO<sub>2</sub> to fuels and chemicals is a primary goal in energy and environmental research. In this work, density functional theory (DFT) is used to study possible reaction mechanisms for the conversion of CO<sub>2</sub> and C<sub>2</sub>H<sub>6</sub> to propanoic acid over a gold‐exchanged MCM‐22 zeolite catalyst. The reaction begins with the activation of ethane to produce a gold ethyl hydride intermediate. Hydrogen transfers to the framework oxygen leads then to gold ethyl adsorbed on the Brønsted‐acid site. The energy barriers for these steps of ethane activation are 9.3 and 16.3 kcal mol<sup>−1</sup>, respectively. Two mechanisms of propanoic acid formation are investigated. In the first one, the insertion of CO<sub>2</sub> into the AuH bond of the first intermediate yields gold carboxyl ethyl as subsequent intermediate. This is then converted to propanoic acid by forming the relevant CC bond. The activation energy of the rate‐determining step of this pathway is 48.2 kcal mol<sup>−1</sup>. In the second mechanism, CO<sub>2</sub> interacts with gold ethyl adsorbed on the Brønsted‐acid site. Propanoic acid is formed via protonation of CO<sub>2</sub> by the Brønsted acid and the simultaneous formation of a bond between CO<sub>2</sub> and the ethyl group. The activation energy there is 44.2 kcal mol<sup>−1</sup>, favoring this second pathway at<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Finding novel catalysts for the direct conversion of CO<sub>2</sub> to fuels and chemicals is a primary goal in energy and environmental research. In this work, density functional theory (DFT) is used to study possible reaction mechanisms for the conversion of CO<sub>2</sub> and C<sub>2</sub>H<sub>6</sub> to propanoic acid over a gold‐exchanged MCM‐22 zeolite catalyst. The reaction begins with the activation of ethane to produce a gold ethyl hydride intermediate. Hydrogen transfers to the framework oxygen leads then to gold ethyl adsorbed on the Brønsted‐acid site. The energy barriers for these steps of ethane activation are 9.3 and 16.3 kcal mol<sup>−1</sup>, respectively. Two mechanisms of propanoic acid formation are investigated. In the first one, the insertion of CO<sub>2</sub> into the AuH bond of the first intermediate yields gold carboxyl ethyl as subsequent intermediate. This is then converted to propanoic acid by forming the relevant CC bond. The activation energy of the rate‐determining step of this pathway is 48.2 kcal mol<sup>−1</sup>. In the second mechanism, CO<sub>2</sub> interacts with gold ethyl adsorbed on the Brønsted‐acid site. Propanoic acid is formed via protonation of CO<sub>2</sub> by the Brønsted acid and the simultaneous formation of a bond between CO<sub>2</sub> and the ethyl group. The activation energy there is 44.2 kcal mol<sup>−1</sup>, favoring this second pathway at least at low temperatures. Gold‐exchanged MCM‐22 zeolite can therefore, at least in principle, be used as the catalyst for producing propanoic acid from CO<sub>2</sub> and ethane.</p> </abstract> … (more)
- Is Part Of:
- Chemphyschem. Volume 15:Issue 3(2014)
- Journal:
- Chemphyschem
- Issue:
- Volume 15:Issue 3(2014)
- Issue Display:
- Volume 15, Issue 3 (2014)
- Year:
- 2014
- Volume:
- 15
- Issue:
- 3
- Issue Sort Value:
- 2014-0015-0003-0000
- Page Start:
- 514
- Page End:
- 520
- Publication Date:
- 2013-12-20
- Subjects:
- Chemistry, Physical and theoretical -- Periodicals
541.05 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7641 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cphc.201300931 ↗
- Languages:
- English
- ISSNs:
- 1439-4235
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3172.310500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 2961.xml