Please use this identifier to cite or link to this item: https://doi.org/10.1039/a809644i
DC FieldValue
dc.titleNanosized hydroxyapatite powders from microemulsions and emulsions stabilized by a biodegradable surfactant
dc.contributor.authorLim, G.K.
dc.contributor.authorWang, J.
dc.contributor.authorNg, S.C.
dc.contributor.authorGan, L.M.
dc.date.accessioned2014-10-16T08:34:59Z
dc.date.available2014-10-16T08:34:59Z
dc.date.issued1999
dc.identifier.citationLim, G.K., Wang, J., Ng, S.C., Gan, L.M. (1999). Nanosized hydroxyapatite powders from microemulsions and emulsions stabilized by a biodegradable surfactant. Journal of Materials Chemistry 9 (7) : 1635-1639. ScholarBank@NUS Repository. https://doi.org/10.1039/a809644i
dc.identifier.issn09599428
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/94350
dc.description.abstractUltrafine hydroxyapatite powders have been successfully synthesized in inverse microemulsions and emulsions consisting of petroleum ether as the oil phase, 1.0 M CaCl2 solution as the aqueous phase and biodegradable KB6ZA as the surfactant. The titration of 0.6 M (NH4)2HPO4 aqueous solution into the inverse microemulsion and emulsions containing 25.0 and 35.0 wt% aqueous phase, resulted in hydroxyapatite precursors that were nanometer sized and more or less spherical in morphology. However, they underwent a considerable degree of particle coarsening when calcined at 650 °C for 6 h. A nanocrystalline hydroxyapatite powder, which exhibited a dendritic agglomerate morphology, was synthesized in an oil-in-water emulsion containing 90.0 wt% aqueous phase. It shows an average particle size of 25 nm upon calcination at 650 °C for 6 h, as little particle coarsening and growth in crystallite size were observed at the calcination temperature. The inverse microemulsion- and emulsion-derived hydroxyapatites exhibit a degree of type B carbonate substitution, which cannot be eliminated by calcination in air at 650 °C.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/a809644i
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.contributor.departmentMATERIALS SCIENCE
dc.description.doi10.1039/a809644i
dc.description.sourcetitleJournal of Materials Chemistry
dc.description.volume9
dc.description.issue7
dc.description.page1635-1639
dc.description.codenJMACE
dc.identifier.isiut000081372600041
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