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Synthesis and characterization of precursors for group II metal aluminates

dc.contributor.authorNarayanan, Ramasubramanianen_US
dc.contributor.authorLaine, Richard M.en_US
dc.date.accessioned2006-04-28T16:51:04Z
dc.date.available2006-04-28T16:51:04Z
dc.date.issued1997-10en_US
dc.identifier.citationNarayanan, Ramasubramanian; Laine, Richrad M. (1997)."Synthesis and characterization of precursors for group II metal aluminates." Applied Organometallic Chemistry 11(10-11): 919-927. <http://hdl.handle.net/2027.42/38300>en_US
dc.identifier.issn0268-2605en_US
dc.identifier.issn1099-0739en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/38300
dc.description.abstractPrecursors to Group II metal aluminates (MAI 2 O 4 , M=Mg, Ca, Ba, Sr) are synthesized from inexpensive starting materials including Group II metal oxides/hydroxides, Al(OH) 3 , triethanolamine (TEA) and ethylene glycol, in a one-pot synthesis process. The precursors are soluble in common organic solvents and can be handled in moist air for a reasonable period of time. On pyrolysis in air to 1200 °C, all three precursors transform to the corresponding Group II metal aluminates. A termetallic double alkoxide, ‘ionomer-like’ structure is proposed, wherein the alkaline-earth metal is encapsulated by a TEA molecule bridging two alumatrane units. The precursors were characterized using TGA, NMR, mass spectroscopy and elemental analyses, and the pyrolysed precursors were briefly characterized using x-ray diffraction analysis. © 1997 John Wiley & Sons, Ltd.en_US
dc.format.extent205126 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherJohn Wiley & Sons, Ltd.en_US
dc.subject.otherChemistryen_US
dc.subject.otherIndustrial Chemistry and Chemical Engineeringen_US
dc.titleSynthesis and characterization of precursors for group II metal aluminatesen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Materials Science and Engineering and Department of Chemistry, 2510, G. G. Brown, 2300, Hayward Ave, University of Michigan, Ann Arbor, MI 48109-2136, USA ; Department of Materials Science and Engineering and Department of Chemistry, 2510, G. G. Brown, 2300, Hayward Ave, University of Michigan, Ann Arbor, MI 48109-2136, USAen_US
dc.contributor.affiliationumDepartment of Materials Science and Engineering and Department of Chemistry, 2510, G. G. Brown, 2300, Hayward Ave, University of Michigan, Ann Arbor, MI 48109-2136, USAen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/38300/1/666_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/(SICI)1099-0739(199710/11)11:10/11<919::AID-AOC666>3.0.CO;2-Zen_US
dc.identifier.sourceApplied Organometallic Chemistryen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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