liu.seSearch for publications in DiVA
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • oxford
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Hydrogen permeation through surface modified Pd and PdAg membranes
Linköping University, The Institute of Technology. Linköping University, Department of Physics, Chemistry and Biology.
Linköping University, The Institute of Technology. Linköping University, Department of Physics, Chemistry and Biology, Applied Physics .
2001 (English)In: Journal of Membrane Science, ISSN 0376-7388, E-ISSN 1873-3123, Vol. 193, no 1, p. 35-47Article in journal (Refereed) Published
Abstract [en]

The hydrogen permeation through surface modified Pd and Pd70Ag30 membranes has been studied at temperatures between 100 and 350°C. Silver has been evaporated on Pd and Pd70Ag30 foils with a thickness of 25µm in order to study the role of the surface composition in comparison with the membrane bulk composition. The Pd70Ag30-based membranes display the largest permeation rates at temperatures below 200°C, while Pd membranes with 20Å silver evaporated on the upstream side show the largest permeation rates above 200°C. There are, consequently, different rate limiting processes above and below 200°C: at temperatures below 200°C, the bulk diffusion through the membrane is rate limiting, while at temperatures above 200°C, the influence of the surface composition starts to become significant. It has further been concluded that a sharp silver concentration gradient from the surface to the bulk is important for the hydrogen permeation rate at temperatures above 200°C. Adding oxygen to the hydrogen supply will almost totally inhibit the hydrogen permeation rate when a pure Pd membrane surface is facing the upstream side, while for silver-containing surfaces the presence of oxygen has almost no effect. On a clean Pd surface, oxygen effectively consumes adsorbed hydrogen in a water forming reaction. With Ag on the surface, no water formation is detected. Co-supplied CO inhibits the permeation of hydrogen in a similar manner on all studied membrane surfaces, independent of surface silver content. © 2001 Elsevier Science B.V. All rights reserved.

Place, publisher, year, edition, pages
2001. Vol. 193, no 1, p. 35-47
Keywords [en]
Hydrogen, Oxygen, Palladium, Permeation, Silver
National Category
Engineering and Technology
Identifiers
URN: urn:nbn:se:liu:diva-47235DOI: 10.1016/S0376-7388(01)00414-8OAI: oai:DiVA.org:liu-47235DiVA, id: diva2:268131
Available from: 2009-10-11 Created: 2009-10-11 Last updated: 2021-12-01
In thesis
1. Hydrogen Extraction with Palladium Based Membranes
Open this publication in new window or tab >>Hydrogen Extraction with Palladium Based Membranes
2000 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Palladium membranes are commercially used to purify hydrogen gas and in dehydrogenation reactions. The combination of the catalytic ability of the membrane surface and the selectivity of hydrogen permeation offers a tool to extract pure hydrogen and to shift a dehydrogenation reaction towards the product side. In this thesis, hydrogen extraction over palladium and palladium-silver based membranes both from different gas mixtures and from dehydrogenated organic molecules is investigated. The aim has been to find the optimal conditions for hydrogen extraction in different environments.

The hydrogen permeation rate has been shown to depend on both silver concentration on the surface and in the bulk of a palladium based membrane. The diffusion through the membrane is the rate limiting step in the permeation process of most studied membranes. For a palladium membrane with 20 Å silver deposited on the upstream surface, the surface reactions, however, become rate limiting.

Co-adsorbed oxygen will inhibit hydrogen permeation by blocking hydrogen adsorption sites and by consuming already adsorbed hydrogen in the water forming reaction on Pd membrane surfaces. On Pd70Ag30 membranes, however, oxygen has no effect on the hydrogen permeation rate, mainly due to an effective hydrogen dissolution into silver and a strongly reduced water formation rate. CO blocks hydrogen adsorption sites on both Pd and PdAg membranes effectively below 150°C, but above 300°C, CO has almost no effect on hydrogen permeation.

Hydrogen can also be extracted through the dehydrogenation of organic molecules. A steady and continuous dehydrogenation of methanol and ethanol, and a subsequent hydrogen permeation, can be maintained in the presence of oxygen through both Pd and PdAg membranes. Without oxygen, a blocking contaminating layer is formed from the decomposition products, which prevents alcohol adsorption and thus also the hydrogen permeation. The hydrogen yield is larger over PdAg membranes than over Pd membranes mainly due to a smaller hydrogen consumption in the water forming reaction, but also due to a larger conversion of the alcohol on PdAg.

The long time objective of this research has been to develop a method to extract hydrogen from anaerobic bacteria degradation of organic waste material in a co-operation project with microbiologists at the Department of Water and Environmental Studies at Linköping University. The selectivity towards hydrogen permeation in palladium membranes offers a tool to obtain clean hydrogen, which can be used as an energy carrier. By draining the bacteria culture of hydrogen, and thereby reducing the partial pressure of hydrogen, the fermentation process is directed towards a higher production of hydrogen.

Place, publisher, year, edition, pages
Linköping: Linköping University, 2000. p. 55
Series
Linköping Studies in Science and Technology. Dissertations, ISSN 0345-7524 ; 651
National Category
Organic Chemistry
Identifiers
urn:nbn:se:liu:diva-181555 (URN)917219832X (ISBN)
Public defence
2000-10-20, Planck, Fysikhuset, Linköpings universitet, Linköping, 10:20
Opponent
Available from: 2021-12-01 Created: 2021-12-01 Last updated: 2023-03-13Bibliographically approved

Open Access in DiVA

No full text in DiVA

Other links

Publisher's full text

Authority records

Ekedahl, Lars-GunnarDannetun, Helen

Search in DiVA

By author/editor
Ekedahl, Lars-GunnarDannetun, Helen
By organisation
The Institute of TechnologyDepartment of Physics, Chemistry and BiologyApplied Physics
In the same journal
Journal of Membrane Science
Engineering and Technology

Search outside of DiVA

GoogleGoogle Scholar

doi
urn-nbn

Altmetric score

doi
urn-nbn
Total: 362 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • oxford
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf