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Characterisation of Mg–x wt.% FeTi (x = 5–30) and Mg–40 wt.% FeTiMn hydrogen absorbing materials prepared by mechanical alloying
Composites based on Mg with intermetallic FeTi (up to 30wt.%) and FeTiMn (40wt.%) were prepared by mechanical alloying for evaluation of their hydrogen storage characteristics. In the first case FeTi was prepared by mechanical alloying and subsequently milled with Mg under argon in different proport...
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Published in: | Journal of alloys and compounds 2004-12, Vol.384 (1-2), p.283-295 |
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creator | Vijay, R. Sundaresan, R. Maiya, M.P. Srinivasa Murthy, S. Fu, Y. Klein, H.-P. Groll, M. |
description | Composites based on Mg with intermetallic FeTi (up to 30wt.%) and FeTiMn (40wt.%) were prepared by mechanical alloying for evaluation of their hydrogen storage characteristics. In the first case FeTi was prepared by mechanical alloying and subsequently milled with Mg under argon in different proportions. Powders milled under argon had to be activated by remilling under hydrogen. In the second case FeTiMn prepared by melting was milled together with MgH2 under hydrogen. Hydrogen storage characteristics, pressure-composition isotherms and kinetics were investigated under different parameters. Among the FeTi composites, Mg–5wt.% FeTi had the maximum absorption capacity of 5.80wt.% at 300°C and 5.12wt.% at 200°C. At 300°C the initial desorption rate was the highest for Mg–10wt.% FeTi, but its final desorption capacity was less than that of Mg–5wt.% FeTi. None of the compositions showed any desorption at 200°C. In the case of composites with FeTiMn, absorption and desorption temperatures decreased by ball milling and higher storage capacities were achieved. In Mg–40wt.% FeTiMn, the lowest absorption and desorption temperatures were 80 and 240°C, respectively, with the material absorbing 4wt.% hydrogen even at 80°C. The kinetics improved with increasing milling time. |
doi_str_mv | 10.1016/j.jallcom.2004.04.115 |
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In the first case FeTi was prepared by mechanical alloying and subsequently milled with Mg under argon in different proportions. Powders milled under argon had to be activated by remilling under hydrogen. In the second case FeTiMn prepared by melting was milled together with MgH2 under hydrogen. Hydrogen storage characteristics, pressure-composition isotherms and kinetics were investigated under different parameters. Among the FeTi composites, Mg–5wt.% FeTi had the maximum absorption capacity of 5.80wt.% at 300°C and 5.12wt.% at 200°C. At 300°C the initial desorption rate was the highest for Mg–10wt.% FeTi, but its final desorption capacity was less than that of Mg–5wt.% FeTi. None of the compositions showed any desorption at 200°C. In the case of composites with FeTiMn, absorption and desorption temperatures decreased by ball milling and higher storage capacities were achieved. In Mg–40wt.% FeTiMn, the lowest absorption and desorption temperatures were 80 and 240°C, respectively, with the material absorbing 4wt.% hydrogen even at 80°C. 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In the first case FeTi was prepared by mechanical alloying and subsequently milled with Mg under argon in different proportions. Powders milled under argon had to be activated by remilling under hydrogen. In the second case FeTiMn prepared by melting was milled together with MgH2 under hydrogen. Hydrogen storage characteristics, pressure-composition isotherms and kinetics were investigated under different parameters. Among the FeTi composites, Mg–5wt.% FeTi had the maximum absorption capacity of 5.80wt.% at 300°C and 5.12wt.% at 200°C. At 300°C the initial desorption rate was the highest for Mg–10wt.% FeTi, but its final desorption capacity was less than that of Mg–5wt.% FeTi. None of the compositions showed any desorption at 200°C. In the case of composites with FeTiMn, absorption and desorption temperatures decreased by ball milling and higher storage capacities were achieved. In Mg–40wt.% FeTiMn, the lowest absorption and desorption temperatures were 80 and 240°C, respectively, with the material absorbing 4wt.% hydrogen even at 80°C. The kinetics improved with increasing milling time.</description><subject>Cross-disciplinary physics: materials science; rheology</subject><subject>Exact sciences and technology</subject><subject>High-energy ball milling</subject><subject>Hydrogen storage materials</subject><subject>Materials science</subject><subject>Materials synthesis; materials processing</subject><subject>Physics</subject><subject>Scanning electron microscopy</subject><subject>X-ray diffraction</subject><issn>0925-8388</issn><issn>1873-4669</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNqNkc9q3DAQxkVpodukj1DQJaU92BnZli0fSilLkxYSeknPQpZGu1psaSs5afbWU18gb5gnqZZdyDGFgYHh982_j5B3DEoGrD3flBs1jjpMZQXQlDkY4y_IgomuLpq27V-SBfQVL0QtxGvyJqUNALC-Zgvyd7lWUekZo0tqdsHTYOn16vHPwz39PZdn9AJvHP1wTz9Rnos1fKTKmwPRwBNy7el6Z2JYoadqSCEOzq_opPaN1ZjoNuJWRTR02NEJ9Vp5p9VI895hl8lT8spmDN8e8wn5efH1ZvmtuPpx-X355arQTQNzYSpUHE1VQQdCdba1vRqMYK1ptIEBOIfOauwaY60esG1RiKauOm4NAw19fULeH_puY_h1i2mWk0sax1F5DLdJVj2reVf9ByhA9L3gGeQHUMeQUkQrt9FNKu4kA7m3R27k0R65t0fmyPZk3dlxgEr5EzYqr116Ere8yidD5j4fOMxvuXMYZdIOvUbjIupZmuCemfQPWdWqhg</recordid><startdate>20041214</startdate><enddate>20041214</enddate><creator>Vijay, R.</creator><creator>Sundaresan, R.</creator><creator>Maiya, M.P.</creator><creator>Srinivasa Murthy, S.</creator><creator>Fu, Y.</creator><creator>Klein, H.-P.</creator><creator>Groll, M.</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8BQ</scope><scope>8FD</scope><scope>H8D</scope><scope>JG9</scope><scope>L7M</scope><scope>7TB</scope><scope>FR3</scope></search><sort><creationdate>20041214</creationdate><title>Characterisation of Mg–x wt.% FeTi (x = 5–30) and Mg–40 wt.% FeTiMn hydrogen absorbing materials prepared by mechanical alloying</title><author>Vijay, R. ; Sundaresan, R. ; Maiya, M.P. ; Srinivasa Murthy, S. ; Fu, Y. ; Klein, H.-P. ; Groll, M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c440t-d2ea5ed220708a7f6f9abd816d4cd0b05507fce74dffcbe66e8843275fd10c093</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Cross-disciplinary physics: materials science; rheology</topic><topic>Exact sciences and technology</topic><topic>High-energy ball milling</topic><topic>Hydrogen storage materials</topic><topic>Materials science</topic><topic>Materials synthesis; materials processing</topic><topic>Physics</topic><topic>Scanning electron microscopy</topic><topic>X-ray diffraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vijay, R.</creatorcontrib><creatorcontrib>Sundaresan, R.</creatorcontrib><creatorcontrib>Maiya, M.P.</creatorcontrib><creatorcontrib>Srinivasa Murthy, S.</creatorcontrib><creatorcontrib>Fu, Y.</creatorcontrib><creatorcontrib>Klein, H.-P.</creatorcontrib><creatorcontrib>Groll, M.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Aerospace Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Engineering Research Database</collection><jtitle>Journal of alloys and compounds</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vijay, R.</au><au>Sundaresan, R.</au><au>Maiya, M.P.</au><au>Srinivasa Murthy, S.</au><au>Fu, Y.</au><au>Klein, H.-P.</au><au>Groll, M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterisation of Mg–x wt.% FeTi (x = 5–30) and Mg–40 wt.% FeTiMn hydrogen absorbing materials prepared by mechanical alloying</atitle><jtitle>Journal of alloys and compounds</jtitle><date>2004-12-14</date><risdate>2004</risdate><volume>384</volume><issue>1-2</issue><spage>283</spage><epage>295</epage><pages>283-295</pages><issn>0925-8388</issn><eissn>1873-4669</eissn><abstract>Composites based on Mg with intermetallic FeTi (up to 30wt.%) and FeTiMn (40wt.%) were prepared by mechanical alloying for evaluation of their hydrogen storage characteristics. In the first case FeTi was prepared by mechanical alloying and subsequently milled with Mg under argon in different proportions. Powders milled under argon had to be activated by remilling under hydrogen. In the second case FeTiMn prepared by melting was milled together with MgH2 under hydrogen. Hydrogen storage characteristics, pressure-composition isotherms and kinetics were investigated under different parameters. Among the FeTi composites, Mg–5wt.% FeTi had the maximum absorption capacity of 5.80wt.% at 300°C and 5.12wt.% at 200°C. At 300°C the initial desorption rate was the highest for Mg–10wt.% FeTi, but its final desorption capacity was less than that of Mg–5wt.% FeTi. None of the compositions showed any desorption at 200°C. In the case of composites with FeTiMn, absorption and desorption temperatures decreased by ball milling and higher storage capacities were achieved. In Mg–40wt.% FeTiMn, the lowest absorption and desorption temperatures were 80 and 240°C, respectively, with the material absorbing 4wt.% hydrogen even at 80°C. The kinetics improved with increasing milling time.</abstract><cop>Lausanne</cop><pub>Elsevier B.V</pub><doi>10.1016/j.jallcom.2004.04.115</doi><tpages>13</tpages></addata></record> |
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subjects | Cross-disciplinary physics: materials science rheology Exact sciences and technology High-energy ball milling Hydrogen storage materials Materials science Materials synthesis materials processing Physics Scanning electron microscopy X-ray diffraction |
title | Characterisation of Mg–x wt.% FeTi (x = 5–30) and Mg–40 wt.% FeTiMn hydrogen absorbing materials prepared by mechanical alloying |
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