Performance of Mn-based H2S sorbents in dry, reducing atmosphere – Manganese oxide support effects. (15th May 2017)
- Record Type:
- Journal Article
- Title:
- Performance of Mn-based H2S sorbents in dry, reducing atmosphere – Manganese oxide support effects. (15th May 2017)
- Main Title:
- Performance of Mn-based H2S sorbents in dry, reducing atmosphere – Manganese oxide support effects
- Authors:
- Chytil, Svatopluk
Kure, Milly
Lødeng, Rune
Blekkan, Edd A. - Abstract:
- Highlights: Additive effect observed for cerium supported manganese oxide due to H2 S sorption on the support as well as on the Mn oxide. Superior stability of zirconium supported Mn oxide in H2 . Strong metal oxide-support interaction influences the sorbent performance. Abstract: High temperature H2 S sorbents comprising manganese oxide (15 wt.%) supported on TiO2, ZrO2, CeO2 and Al2 O3 were prepared by wet impregnation using Mn(NO3 )2 ·4H2 O as Mn precursor. Upon activation in H2, the sorbent performance testing was conducted at 650 °C in a model gas mixture with a composition of 0.4 vol.% of H2 S in 40 vol.% of H2, the balance being inert gas. Sorbent regeneration was performed at 650 °C with 5.2 vol.% of O2 in N2 . The initial sorption performance is first reported for the parent (Mn-free) supports showing a considerable H2 S sorption on ZrO2 and CeO2 and a minor sorption on Al2 O3 and TiO2 . The Mn sorbents were subject to 13 sorption/regeneration cycles. The highest initial sorption capacity is reported for cerium supported Mn oxide, which is also the sample that deactivates most. A prolonged exposure to H2 at 650 °C results in a reversible loss of the sorption capacity that was observed for all the samples except for Mn on zirconia suggesting its superior stability in H2 . The supports, fresh and regenerated Mn sorbents were characterized by means of N2 sorption measurements, X-ray Diffraction and Raman spectroscopy. Temperature-Programmed Reduction was performed onHighlights: Additive effect observed for cerium supported manganese oxide due to H2 S sorption on the support as well as on the Mn oxide. Superior stability of zirconium supported Mn oxide in H2 . Strong metal oxide-support interaction influences the sorbent performance. Abstract: High temperature H2 S sorbents comprising manganese oxide (15 wt.%) supported on TiO2, ZrO2, CeO2 and Al2 O3 were prepared by wet impregnation using Mn(NO3 )2 ·4H2 O as Mn precursor. Upon activation in H2, the sorbent performance testing was conducted at 650 °C in a model gas mixture with a composition of 0.4 vol.% of H2 S in 40 vol.% of H2, the balance being inert gas. Sorbent regeneration was performed at 650 °C with 5.2 vol.% of O2 in N2 . The initial sorption performance is first reported for the parent (Mn-free) supports showing a considerable H2 S sorption on ZrO2 and CeO2 and a minor sorption on Al2 O3 and TiO2 . The Mn sorbents were subject to 13 sorption/regeneration cycles. The highest initial sorption capacity is reported for cerium supported Mn oxide, which is also the sample that deactivates most. A prolonged exposure to H2 at 650 °C results in a reversible loss of the sorption capacity that was observed for all the samples except for Mn on zirconia suggesting its superior stability in H2 . The supports, fresh and regenerated Mn sorbents were characterized by means of N2 sorption measurements, X-ray Diffraction and Raman spectroscopy. Temperature-Programmed Reduction was performed on the parent supports and fresh sorbents. The changes in material properties caused by the testing as well as a different degree of a metal oxide-support interaction influencing the sorption performance are discussed. … (more)
- Is Part Of:
- Fuel. Volume 196(2017)
- Journal:
- Fuel
- Issue:
- Volume 196(2017)
- Issue Display:
- Volume 196, Issue 2017 (2017)
- Year:
- 2017
- Volume:
- 196
- Issue:
- 2017
- Issue Sort Value:
- 2017-0196-2017-0000
- Page Start:
- 124
- Page End:
- 133
- Publication Date:
- 2017-05-15
- Subjects:
- Producer gas -- H2S solid sorbents -- Manganese oxides -- Support effect
Fuel -- Periodicals
Coal -- Periodicals
Coal
Fuel
Periodicals
662.6 - Journal URLs:
- http://www.sciencedirect.com/science/journal/latest/00162361 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.fuel.2017.01.087 ↗
- Languages:
- English
- ISSNs:
- 0016-2361
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4048.000000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 938.xml