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dc.contributor.authorLiou, SZCen_US
dc.contributor.authorChen, SYen_US
dc.contributor.authorLiu, DMen_US
dc.date.accessioned2014-12-08T15:37:16Z-
dc.date.available2014-12-08T15:37:16Z-
dc.date.issued2004-12-01en_US
dc.identifier.issn0957-4530en_US
dc.identifier.urihttp://dx.doi.org/10.1007/s10856-004-5733-5en_US
dc.identifier.urihttp://hdl.handle.net/11536/25602-
dc.description.abstractCalcium phosphate ceramics (CPCs) were prepared via an in-situ formation in the presence of polyacrylic acid (PAA) polymer under water-methanol (WM) mixture at room temperature. The PAA polymer was employed as both structure-directing agent and crystallization retardant to manipulate the development of resulting CPCs nano-crystallites which are observed to show a core-shell configuration with a thin layer of PAA molecules. A resulting phase evolution map with respect to the developing phases of calcium-deficient hydroxyapatite (CDHA), beta-tricalcium phosphate (beta-TCP), and an intermediate amorphous calcium phoshate (ACP) that were structurally and spectroscopically identified, was constructed in terms of fractions of water-to-methanol proportions and concentration of PAA. It is found that for the solutions in both water-rich and methanol-rich regions, pure CDHA and beta-TCP instead of intermediate ACP phase can be developed irrespective of the concentration of PAA, respectively. For conditions in between, i.e., with methanol fractions of 15%-90%, ACP appeared only when the PAA fell in a limited concentration range. (C) 2004 Kluwer Academic Publishers.en_US
dc.language.isoen_USen_US
dc.titlePhase development and structural characterization of calcium phosphate ceramics-polyacrylic acid nanocomposites at room temperature in water-methanol mixturesen_US
dc.typeArticleen_US
dc.identifier.doi10.1007/s10856-004-5733-5en_US
dc.identifier.journalJOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINEen_US
dc.citation.volume15en_US
dc.citation.issue12en_US
dc.citation.spage1261en_US
dc.citation.epage1266en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.identifier.wosnumberWOS:000226838200001-
dc.citation.woscount12-
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