Please use this identifier to cite or link to this item: http://dspace.unimap.edu.my:80/xmlui/handle/123456789/84164
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dc.contributor.authorSoojinthiran, Ahtmanathan-
dc.contributorSchool of Materials Engineeringen_US
dc.date2023-12-
dc.date.accessioned2025-06-05T03:16:02Z-
dc.date.available2025-06-05T03:16:02Z-
dc.date.issued2017-06-
dc.identifier.urihttp://dspace.unimap.edu.my:80/xmlui/handle/123456789/84164-
dc.descriptionAccess is limited to UniMAP community.en_US
dc.description.abstractIn this study, 58% SiO₂ - 38% CaO - 4% P₂O₅ bio-glass was synthesised using sol-gel method, pressed into pellets and sintered at three different temperature i.e. 600⁰C, 800⁰C and 1000⁰C. The effect of different sintering temperature on physical, structural and bioactivity properties were investigated using XRD, SEM, FTIR, XRF and TGA/DTA. From this study, it has been found out that by increasing the sintering temperature, the corresponding Si-O-Si bonds also increases in intensity. The increase in the Si-O-Si bond increases the bridging oxygen bonds which is responsible for the crystallinity of the glass. Besides that, the Si-OH bonds is also found to be decreased in intensity which corresponds hydroxyapatite formation. Thus, all these factor affects the bio-activity as the increase in sintering temperature will decrease the bioactivity (less apatite formation).en_US
dc.language.isoenen_US
dc.publisherUniversiti Malaysia Perlis (UniMAP)en_US
dc.subject.otherBio-glassen_US
dc.subject.otherBio- active materialsen_US
dc.subject.otherBio-active glassen_US
dc.titleSynthesis and properties evaluation of sintered bioglass based on 58% SiO₂ - 38% CaO - 4% P₂O₅en_US
dc.typeLearning Objecten_US
dc.contributor.advisorSyed Nuzul Fadzli Syed Adam-
Appears in Collections:School of Materials Engineering (FYP)

Files in This Item:
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Abstract, Acknowledgement.pdf478.69 kBAdobe PDFView/Open
Introduction.pdf477.9 kBAdobe PDFView/Open
Literature Review.pdf758.72 kBAdobe PDFView/Open
Methodology.pdf695.68 kBAdobe PDFView/Open
Result and Discussion.pdf1.65 MBAdobe PDFView/Open
Conclusion.pdf564.32 kBAdobe PDFView/Open
References and Appendices.pdf855.03 kBAdobe PDFView/Open


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