File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Effects of carbon-supported nickel catalysts on MgH2decomposition

TitleEffects of carbon-supported nickel catalysts on MgH<inf>2</inf>decomposition
Authors
Issue Date2008
Citation
Journal of Physical Chemistry C, 2008, v. 112, n. 15, p. 5984-5992 How to Cite?
AbstractThis paper analyzes the improvement of MgH2decomposition by the addition of nickel-based catalysts, mostly carbon-supported nickel catalysts. Our study shows that some experimental parameters such as the catalyst content, its composition, the method of preparation, and milling time strongly affect its activity toward MgH2decomposition. We observe that carbon-supported nickel catalysts have superior performance than those just containing carbon and nickel physically mixed and, especially, than those containing only nickel. This emphasizes the role played by carbon and by the nickel-carbon interaction on the activity of such MgH2-based materials. A decrease, followed by differential scanning calorimetry (DSC), in the decomposition temperature of MgH2of 150 °C can be achieved with some selected supported catalysts. Suitable selection of the catalyst preparation conditions leads to materials for which decomposition of 6.6 wt % hydrogen occurs in just 9 min at 300 °C, in comparison to 240 min required for undoped MgH2, and is stable after five cycles. Comparison between catalysts supported on different carbon materials having similar compositions but different nickel particle size shows no relevant differences in their isothermal decomposition kinetics. © 2008 American Chemical Society.
Persistent Identifierhttp://hdl.handle.net/10722/262903
ISSN
2023 Impact Factor: 3.3
2023 SCImago Journal Rankings: 0.957
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLillo-Ródenas, M. A.-
dc.contributor.authorAguey-Zinsou, K. F.-
dc.contributor.authorCazorla-Amorós, D.-
dc.contributor.authorLinares-Solano, A.-
dc.contributor.authorGuo, Z. X.-
dc.date.accessioned2018-10-08T09:28:46Z-
dc.date.available2018-10-08T09:28:46Z-
dc.date.issued2008-
dc.identifier.citationJournal of Physical Chemistry C, 2008, v. 112, n. 15, p. 5984-5992-
dc.identifier.issn1932-7447-
dc.identifier.urihttp://hdl.handle.net/10722/262903-
dc.description.abstractThis paper analyzes the improvement of MgH2decomposition by the addition of nickel-based catalysts, mostly carbon-supported nickel catalysts. Our study shows that some experimental parameters such as the catalyst content, its composition, the method of preparation, and milling time strongly affect its activity toward MgH2decomposition. We observe that carbon-supported nickel catalysts have superior performance than those just containing carbon and nickel physically mixed and, especially, than those containing only nickel. This emphasizes the role played by carbon and by the nickel-carbon interaction on the activity of such MgH2-based materials. A decrease, followed by differential scanning calorimetry (DSC), in the decomposition temperature of MgH2of 150 °C can be achieved with some selected supported catalysts. Suitable selection of the catalyst preparation conditions leads to materials for which decomposition of 6.6 wt % hydrogen occurs in just 9 min at 300 °C, in comparison to 240 min required for undoped MgH2, and is stable after five cycles. Comparison between catalysts supported on different carbon materials having similar compositions but different nickel particle size shows no relevant differences in their isothermal decomposition kinetics. © 2008 American Chemical Society.-
dc.languageeng-
dc.relation.ispartofJournal of Physical Chemistry C-
dc.titleEffects of carbon-supported nickel catalysts on MgH<inf>2</inf>decomposition-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/jp711749h-
dc.identifier.scopuseid_2-s2.0-43749086931-
dc.identifier.volume112-
dc.identifier.issue15-
dc.identifier.spage5984-
dc.identifier.epage5992-
dc.identifier.eissn1932-7455-
dc.identifier.isiWOS:000254883100044-
dc.identifier.issnl1932-7447-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats