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Transmission electron microscopic confirmation of the morphological predictions of the two-site model for hydroxyapatite dissolution

dc.contributor.authorGriffith, Earl N.en_US
dc.contributor.authorKatdare, Ashoken_US
dc.contributor.authorFox, Jeffrey L.en_US
dc.contributor.authorHiguchi, William I.en_US
dc.date.accessioned2006-04-07T17:05:42Z
dc.date.available2006-04-07T17:05:42Z
dc.date.issued1978-11en_US
dc.identifier.citationGriffith, Earl N., Katdare, Ashok, Fox, Jeffrey L., Higuchi, William I. (1978/11)."Transmission electron microscopic confirmation of the morphological predictions of the two-site model for hydroxyapatite dissolution." Journal of Colloid and Interface Science 67(2): 331-335. <http://hdl.handle.net/2027.42/22739>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WHR-4CT12XW-G0/2/a0ef604e3a343d786be30c9009956598en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/22739
dc.description.abstractHydroxyapatite (HAP) crystals were dissolved under two types of solution conditions designed to produce contrasting dissolution morphologies according to the recently proposed two-site model for HAP dissolution [Fox, J. L., Higuchi, W. I., Fawzi, M. B., and Wu, M. S., J. Colloid Interface Sci., 67, 312 (1978)]. In accordance with this model, dissolution into partially saturated buffers proceeded via formation of holes in the crystals, while dissolution of comparable amounts of material into completely unsaturated buffers showed no such holes. These results show that the two dissolution sites inferred from dissolution kinetics experiments are, in fact, physically distinct sites and that dissolution from site No. 1 results in hole formation. The physical location of site No. 2 is not yet certain.en_US
dc.format.extent4287700 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleTransmission electron microscopic confirmation of the morphological predictions of the two-site model for hydroxyapatite dissolutionen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumCollege of Pharmacy, The University of Michigan, Ann Arbor, Michigan 48109, USAen_US
dc.contributor.affiliationumCollege of Pharmacy, The University of Michigan, Ann Arbor, Michigan 48109, USAen_US
dc.contributor.affiliationumCollege of Pharmacy, The University of Michigan, Ann Arbor, Michigan 48109, USAen_US
dc.contributor.affiliationumCollege of Pharmacy, The University of Michigan, Ann Arbor, Michigan 48109, USAen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/22739/1/0000294.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0021-9797(78)90017-6en_US
dc.identifier.sourceJournal of Colloid and Interface Scienceen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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