Please use this identifier to cite or link to this item: http://repository.kln.ac.lk/handle/123456789/5451
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dc.contributor.authorPremaratne, W.A.P.J.
dc.contributor.authorPriyadarshana, W.M.G.I.
dc.contributor.authorGunawardena, S.H.P.
dc.contributor.authorde Alwis, A.A.P.
dc.date.accessioned2015-02-27T06:24:42Z
dc.date.available2015-02-27T06:24:42Z
dc.date.issued2013
dc.identifierChemistryen_US
dc.identifier.citationPremaratne, W.A.P.J., Priyadarshana, W.M.G.I., Gunawardena, S.H.P. and De Alwis, A.A.P. (2013). Synthesis of Nanosilica from Paddy Husk Ash and Their Surface Functionalization, Journal of Science, University of Kelaniya, 8: 33-48.en_US
dc.identifier.issnChemistry
dc.identifier.issnChemistry
dc.identifier.uri
dc.identifier.urihttp://repository.kln.ac.lk/handle/123456789/5451
dc.description.abstractNanosilica was synthesized by a chemical precipitation process from paddy husk ash (PHA) efficiently and effectively. Surface functionalization of the silica nanoparticles was carried out with oleic acid (C18H34O2). Scanning electron micrographs (SEM) data showed that the nanosilica particle size was in the range of 50-70 nm and they were in the agglomerate form. X-ray diffraction (XRD) analysis data revealed that synthesized nanosilica was in amorphous form showing a strong broad peak at 22.14o (2). Fourier transform infrared spectroscopy (FT-IR) data supported the presence of hydrogen bonded silanol group and siloxane groups in nanosilica. Surface functionalized nanosilica with oleic acid was characterized using thermogravimetric analysis (TGA) and FT-IR methods. FT-IR experimental data showed that the modified nanosilica formed the ester bonding between silanol group in nanosilica and the carboxylic group of oleic acid with a successful functionalization.en_US
dc.language.isoenen_US
dc.publisherUniversity of Kelaniyaen_US
dc.subjectNanosilicaen_US
dc.subjectPaddy husk ashen_US
dc.subjectOleic aciden_US
dc.subjectFunctionalizationen_US
dc.titleSynthesis of Nanosilica from Paddy Husk Ash and Their Surface Functionalizationen_US
dc.typeArticleen_US
Appears in Collections:Volume 08 - 2013

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