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Article: Nano-structured MgH2 catalyzed by TiC nanoparticles for hydrogen storage

TitleNano-structured MgH<inf>2</inf> catalyzed by TiC nanoparticles for hydrogen storage
Authors
KeywordsNanoparticles
Mechanical milling
Microstructure
Hydrogen storage
MgH2
Absorption/desorption kinetics
TiC
Issue Date2011
Citation
Journal of Chemical Technology and Biotechnology, 2011, v. 86, n. 1, p. 69-74 How to Cite?
AbstractBackground: Magnesium hydride is considered to be a promising hydrogen storage material because of its high gravimetric and volumetric storage capacities. However, its slow kinetics and high desorption temperature of > 300 °C limit practical applications. In this work, TiC nanoparticles were selected to modify the hydrogen storage properties of MgH2. Composite mixtures (MgH2 + TiC) were prepared using both cryogenic milling and high-energy ball milling. RESULTS: The resulting morphology and crystallite structure of the composites were identified by scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray diffraction (XRD). The milled samples show good mixing of the hydride and carbide particles, with MgH2 particles around 0.09-1 μm and TiC particles 10-20 nm. The (MgH2 + TiC) composites consist of γ-MgH2, β-MgH2 and TiC. MgH2 nano-crystallites of 25 nm were formed after cryomilling. Thermogravimetry reveals that the composites release ~6.5 mass % hydrogen from 190-400 °C at a heating rate of 10 °C min-1 under He flow, with the onset and peak temperatures at 190 and 280 °C, respectively, for the (MgH2 + TiC) after 8 h cryomilling and 60 h ball milling. CONCLUSION: Results indicate that TiC is an effective catalyst for hydrogen desorption of MgH2. © 2010 Society of Chemical Industry.
Persistent Identifierhttp://hdl.handle.net/10722/295120
ISSN
2021 Impact Factor: 3.709
2020 SCImago Journal Rankings: 0.640
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorTian, Mi-
dc.contributor.authorShang, Congxiao-
dc.date.accessioned2021-01-05T04:59:06Z-
dc.date.available2021-01-05T04:59:06Z-
dc.date.issued2011-
dc.identifier.citationJournal of Chemical Technology and Biotechnology, 2011, v. 86, n. 1, p. 69-74-
dc.identifier.issn0268-2575-
dc.identifier.urihttp://hdl.handle.net/10722/295120-
dc.description.abstractBackground: Magnesium hydride is considered to be a promising hydrogen storage material because of its high gravimetric and volumetric storage capacities. However, its slow kinetics and high desorption temperature of > 300 °C limit practical applications. In this work, TiC nanoparticles were selected to modify the hydrogen storage properties of MgH2. Composite mixtures (MgH2 + TiC) were prepared using both cryogenic milling and high-energy ball milling. RESULTS: The resulting morphology and crystallite structure of the composites were identified by scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray diffraction (XRD). The milled samples show good mixing of the hydride and carbide particles, with MgH2 particles around 0.09-1 μm and TiC particles 10-20 nm. The (MgH2 + TiC) composites consist of γ-MgH2, β-MgH2 and TiC. MgH2 nano-crystallites of 25 nm were formed after cryomilling. Thermogravimetry reveals that the composites release ~6.5 mass % hydrogen from 190-400 °C at a heating rate of 10 °C min-1 under He flow, with the onset and peak temperatures at 190 and 280 °C, respectively, for the (MgH2 + TiC) after 8 h cryomilling and 60 h ball milling. CONCLUSION: Results indicate that TiC is an effective catalyst for hydrogen desorption of MgH2. © 2010 Society of Chemical Industry.-
dc.languageeng-
dc.relation.ispartofJournal of Chemical Technology and Biotechnology-
dc.subjectNanoparticles-
dc.subjectMechanical milling-
dc.subjectMicrostructure-
dc.subjectHydrogen storage-
dc.subjectMgH2-
dc.subjectAbsorption/desorption kinetics-
dc.subjectTiC-
dc.titleNano-structured MgH<inf>2</inf> catalyzed by TiC nanoparticles for hydrogen storage-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1002/jctb.2479-
dc.identifier.scopuseid_2-s2.0-78650048610-
dc.identifier.volume86-
dc.identifier.issue1-
dc.identifier.spage69-
dc.identifier.epage74-
dc.identifier.eissn1097-4660-
dc.identifier.isiWOS:000286291700011-
dc.identifier.issnl0268-2575-

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