A metal hydride-polymer composite for hydrogen storage applications

TitleA metal hydride-polymer composite for hydrogen storage applications
Publication TypeArticolo su Rivista peer-reviewed
Year of Publication2009
AuthorsPentimalli, M., Padella F., La Barbera A., Pilloni L., and Imperi E.
JournalEnergy Conversion and Management
Volume50
Pagination3140-3146
ISSN01968904
KeywordsABS, Active metals, Alloy powder, Ball milling, Complexation, composite, Composite materials, Dimensional integrity, Fine powders, Hot pressing, Hydrides, Hydriding-dehydriding properties, Hydrogen, Hydrogen cycling, Hydrogen storage, Kinetic properties, Lithium batteries, Loading capacities, Magnetic tape, Materials properties, matrix, Metal hydride, Metal hydrides, Metal particle, Metal powder, Metals, Milling (machining), Milling machines, Number of cycles, Pelletizing, Polymer composite, Polymer weights, Polymeric material, Polymeric matrices, Polymers, Powder metals, Practical use, SEM observation
Abstract

To address the issue of the breakdown into fine powders that occurs in the practical use of metal hydrides, the possibility of using a polymeric material as a matrix that contains the active metal particles was experimentally assessed. A ball milling approach in the tumbling mode was used to develop a metal hydride-polymer composite with a high metal to polymer weight ratio. The alloy powder was blended with the polymer and a coating of the metal particles was obtained. The composite was consolidated by hot pressing and the pellets were characterized in terms of their hydriding-dehydriding properties. The materials did not show significant losses in either loading capacity or kinetic properties. The polymeric matrix resulted as being stable under hydrogen cycling. Further, from SEM observation it was confirmed that the metal powders remained embedded in the polymeric matrix even after a number of cycles and that the overall dimensional integrity was retained. © 2009 Elsevier Ltd. All rights reserved.

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URLhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-70349456503&doi=10.1016%2fj.enconman.2009.08.021&partnerID=40&md5=4de8b3a818ca67321564642eaf09ef81
DOI10.1016/j.enconman.2009.08.021