Development and characterization of thermally stable supported V–W–TiO2 catalysts for mobile NH3–SCR applications. (February 2015)
- Record Type:
- Journal Article
- Title:
- Development and characterization of thermally stable supported V–W–TiO2 catalysts for mobile NH3–SCR applications. (February 2015)
- Main Title:
- Development and characterization of thermally stable supported V–W–TiO2 catalysts for mobile NH3–SCR applications
- Authors:
- Beale, Andrew M.
Lezcano-Gonzalez, Ines
Maunula, Teuvo
Palgrave, Robert G. - Abstract:
- <abstract> <title> <x content-type="archive" xml:space="preserve">Abstract</x> </title> <p> <graphic xlink:href="ark:/27927/pgh3xb8196r" position="anchor" orientation="portrait" xmlns:xlink="http://www.w3.org/1999/xlink" /> </p> <p>Vanadium based catalysts supported on a mixture of tungsten and titanium oxide (V<sub>2</sub>O<sub>5</sub>/WO<sub>3</sub>–TiO<sub>2</sub>) are known to be highly active for ammonia selective catalytic reduction (NH<sub>3</sub>–SCR) of NO<sub>x</sub> species for heavy-duty mobile applications. However they are also known to be sensitive to high temperatures which leads to both sintering of the anatase TiO<sub>2</sub> support and a first order phase transition to rutile at temperatures &gt;600°C. Here we report our attempts to use SiO<sub>2</sub> to stabilize the TiO<sub>2</sub> anatase phase and to compare its catalytic activity with that of a non-stabilized V<sub>2</sub>O<sub>5</sub>/WO<sub>3</sub>–TiO<sub>2</sub> catalyst after thermal aging up to 800°C. Detailed characterization using spectroscopic (Raman, UV–vis, X-ray absorption spectroscopy), scattering and techniques providing information on the catalytic surface (Brunauer–Emmet–Teller, NH<sub>3</sub> adsorption) have also been performed in order to understand the impact of high temperatures on component speciation and the catalytic interface. Results show that non-stabilized V<sub>2</sub>O<sub>5</sub>/WO<sub>3</sub>–TiO<sub>2</sub> catalysts are initially stable after thermal aging at 600°C<abstract> <title> <x content-type="archive" xml:space="preserve">Abstract</x> </title> <p> <graphic xlink:href="ark:/27927/pgh3xb8196r" position="anchor" orientation="portrait" xmlns:xlink="http://www.w3.org/1999/xlink" /> </p> <p>Vanadium based catalysts supported on a mixture of tungsten and titanium oxide (V<sub>2</sub>O<sub>5</sub>/WO<sub>3</sub>–TiO<sub>2</sub>) are known to be highly active for ammonia selective catalytic reduction (NH<sub>3</sub>–SCR) of NO<sub>x</sub> species for heavy-duty mobile applications. However they are also known to be sensitive to high temperatures which leads to both sintering of the anatase TiO<sub>2</sub> support and a first order phase transition to rutile at temperatures &gt;600°C. Here we report our attempts to use SiO<sub>2</sub> to stabilize the TiO<sub>2</sub> anatase phase and to compare its catalytic activity with that of a non-stabilized V<sub>2</sub>O<sub>5</sub>/WO<sub>3</sub>–TiO<sub>2</sub> catalyst after thermal aging up to 800°C. Detailed characterization using spectroscopic (Raman, UV–vis, X-ray absorption spectroscopy), scattering and techniques providing information on the catalytic surface (Brunauer–Emmet–Teller, NH<sub>3</sub> adsorption) have also been performed in order to understand the impact of high temperatures on component speciation and the catalytic interface. Results show that non-stabilized V<sub>2</sub>O<sub>5</sub>/WO<sub>3</sub>–TiO<sub>2</sub> catalysts are initially stable after thermal aging at 600°C but on heating above this temperature a marked drop in catalytic activity is observed as a result of sintering and phase transformation of Anatase into Rutile TiO<sub>2</sub> and phase segregation of initially highly dispersed WO<sub>3</sub> and polymeric V<sub>2</sub>O<sub>5</sub> into monoclinic WO<sub>3</sub> and V<sub>2</sub>O<sub>3</sub> crystallites. Similar behavior was observed for the 4–5 wt-% of SiO<sub>2</sub>-stabilised sample after aging above 700°C, importantly therefore, offset by some ∼100°C in comparison to the unstabilised sample.</p> </abstract> … (more)
- Is Part Of:
- Catalysis, structure & reactivity. Volume 1:Number 1(2015)
- Journal:
- Catalysis, structure & reactivity
- Issue:
- Volume 1:Number 1(2015)
- Issue Display:
- Volume 1, Issue 1 (2015)
- Year:
- 2015
- Volume:
- 1
- Issue:
- 1
- Issue Sort Value:
- 2015-0001-0001-0000
- Page Start:
- 25
- Page End:
- 34
- Publication Date:
- 2015-02
- Subjects:
- Catalysts -- Periodicals
Catalysis -- Periodicals
Chemistry, Physical and theoretical -- Periodicals
660.2995 - Journal URLs:
- http://www.maneyonline.com/loi/cat ↗
https://www.tandfonline.com/journals/ycsr20 ↗
http://www.tandfonline.com/ ↗ - DOI:
- 10.1179/2055075814Y.0000000005 ↗
- Languages:
- English
- ISSNs:
- 2055-074X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3739.xml