Publication:
Structural and characterisation analysis of zinc-substituted hydroxyapatite with wet chemical precipitation method

dc.contributor.authorsKaracan I., Senturk D., Oktar F.N., Ficai A., Ficai D., Trusca R., Vasile B.S., Gokce H., Ozuyar H.D., Gunduz O.
dc.date.accessioned2022-03-15T02:11:59Z
dc.date.accessioned2026-01-10T18:40:10Z
dc.date.available2022-03-15T02:11:59Z
dc.date.issued2016
dc.description.abstractHydroxyapatite (HAp) is a biocompatible, bioactive and biodegradable biomaterial widely used in the biomedical area. In this work, the synthesis of zinc substituted hydroxyapatite (Zn-HAp) is described. Zn-Hap nano-powders with 0.5, 2, 5, 10 and 25 wt.% zinc were produced by wet chemical synthesis method. The samples were analysed by XRD for determine crystallite size and phase composition of each sample, SEM and HR-TEM for determine the size and shape of the nanoparticles while FTIR was used to identify the chemical changes of the samples. According to the XRD data, the crystallite size decreased when the increase of the zinc concentration. Therefore, HAp structure was observed in all samples except the sample with 25 wt.% Zn where mostly monetite and parascholzite were obtained instead of HAp. Its structure was deformed and also agglomerated by high zinc-content. Copyright © 2016 Inderscience Enterprises Ltd.
dc.identifier.doi10.1504/IJNBM.2016.086110
dc.identifier.issn17528933
dc.identifier.urihttps://hdl.handle.net/11424/247714
dc.language.isoeng
dc.publisherInderscience Publishers
dc.relation.ispartofInternational Journal of Nano and Biomaterials
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectHydroxyapatite
dc.subjectWet chemical synthesis processing
dc.subjectZinc substitution
dc.titleStructural and characterisation analysis of zinc-substituted hydroxyapatite with wet chemical precipitation method
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage204
oaire.citation.issue3-4
oaire.citation.startPage188
oaire.citation.titleInternational Journal of Nano and Biomaterials
oaire.citation.volume6

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