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The Influence Of MoS2on The Phase Structure And Hydrogen Storage Properties Of Magnesium-based Alloys

Posted on:2013-01-13Degree:MasterType:Thesis
Country:ChinaCandidate:Y H JiaFull Text:PDF
GTID:2231330392954876Subject:Chemical processes
Abstract/Summary:PDF Full Text Request
The main advantages of magnesium-based hydrogen storage materials include highhydrogen storage capacity (7.6wt.%), abundance as well as low cost. The materials havebeen investigated for the past decades, however, it cannot be widely applied because of thehigh hydrogen absorption and decomposition temperature and the poor kinetics. In thispaper, a series of composites were prepared using mechanically ball milling, of which thephase structures, kinetics and dehydrogenation thermal desorption were investigated.MoS2can significantly improve the kinetics performance of MgH2. At423K, theMgH2with MoS2absorbs2.7wt.%hydrogen within800s, while the as-milled MgH2absorbs only0.7wt.%hydrogen under the same experimental conditions. For dehydrogenkinetic of MgH2with MoS2,0.55wt.%hydrogen can be desorbed within600s at423K,however, only0.1wt.%of hydrogen is desorbed of the as-milled MgH2. Based on theKissinger plot, the activation energy of the hydrogen desorption processes of MgH2reduces by23.84kJ·mol-1due to the addition of MoS2, indicating that the dehydridingprocess energy barrier of MgH2can be reduced with the catalytic effect of MoS2. MoS2reacts with MgH2to in-situ produce MgS and Mo phases during ball milling process, MgSand Mo phases are found to be stable and always exist in the hydriding/dehydridingprocesses. The MgS and Mo play a synergistic role in facilitating the kineticsimprovement of MgH2.The LaH3and MgH2are produced after dehydrogenation of LaMg3alloy. The effectof LaH3and MoS2in catalyzing MgH2are studied. The LaMg3+17wt.%MoS2compositeis prepared by ball milling. MoS2reduces the onset dehydrogenation temperaturesignificantly and ameliorates the kinetics performance of LaMg3alloy. At423K, thecomposite achieves80%of the maximum hydrogen storage amount is10s, while theLaMg3alloy takes60s. The dehydrogen time for content to reach80%of maximumstorage capacity for the composite is240s at573K, while the LaMg3alloy is450s. Theonset dehydrogenation temperature of LaMg3alloy reduces58K due to the addition ofMoS2. The storage performance improvement of LaMg3alloy is due to the catalysis ofLaH3and the synergistic effect of MgS and Mo. The hydrogen storage property of LaMg7.25Ni1.75with MoS2is investigated. At473K,the uptime for hydrogen content to reach80%of maximum hydrogen storage capacity forthe composite is50s, while the LaMg7.25Ni1.75alloy is100s at the same condition. P-C-Ttest shows that platform pressure of Mg2Ni phase for the composite is higher than that forthe LaMg7.25Ni1.75alloys. The dehydriding enthalpy of Mg2Ni phase for the composite isless than that for LaMg7.25Ni1.75alloy. This proves that Mg2NiH4of the composite is easierto decompose. The DSC shows the onset dehydrogenation temperature of LaMg3alloyreduces about10K due to the addition of MoS2.
Keywords/Search Tags:Mg based hydrogen storage alloy, composite, molybdenum sulfide, phasestructure, hydrogen storage performance
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