نمایش مختصر رکورد

dc.date.accessioned1399-07-09T08:26:02Zfa_IR
dc.date.accessioned2020-09-30T08:26:02Z
dc.date.available1399-07-09T08:26:02Zfa_IR
dc.date.available2020-09-30T08:26:02Z
dc.date.issued2012-04-01en_US
dc.date.issued1391-01-13fa_IR
dc.date.submitted2012-02-15en_US
dc.date.submitted1390-11-26fa_IR
dc.identifier.citation(2012). Formation of Needle Like Hydroxyl Apatite by Polyelectrolyte-modified Inverse Microemulsion Technique. International Journal of Bio-Inorganic Hybrid Nanomaterials, 1(1), 59-65.en_US
dc.identifier.issn2251-8533
dc.identifier.issn2322-4142
dc.identifier.urihttp://ijbihn.iauvaramin.ac.ir/article_632363.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/341313
dc.description.abstractIn this work needle like hydroxy apatite were synthesized in a reverse microemulsion droplets of water in cyclohexane, separated by a cationic surfactant and co-surfactant, in the presence of Na-polyacrylate (PAA) as an anionic polyelectrolyte. Characterization of the as formed HAp nanoparticles at the room temperature were carried out by X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR). Size and morphology of the samples were investigated using scaning and transmission electron microscopy (SEM and TEM). The results obtained confirm incorperation of PAA as a template in controlling of the size and morphology of HAp nanoparticles into the individual microemulsion droplets.en_US
dc.format.extent926
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherIslamic Azad University - Varamin Branchen_US
dc.relation.ispartofInternational Journal of Bio-Inorganic Hybrid Nanomaterialsen_US
dc.subjectCationic surfactanten_US
dc.subjectReverse microemulsion dropleten_US
dc.subjectHydroxy apatiteen_US
dc.subjectAnionic polyelectrolyteen_US
dc.subjectNa-polyacrylateen_US
dc.titleFormation of Needle Like Hydroxyl Apatite by Polyelectrolyte-modified Inverse Microemulsion Techniqueen_US
dc.typeTexten_US
dc.typeResearch Paperen_US
dc.citation.volume1
dc.citation.issue1
dc.citation.spage59
dc.citation.epage65


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