creators_name: Mohamad, D, creators_name: Young, R.J. , creators_name: Mann, A.B. , creators_name: Watts, D.C. , creators_id: dasmawati@kck.usm.my creators_id: creators_id: creators_id: type: article datestamp: 2008-02-02 09:36:17 lastmod: 2008-02-02 09:36:17 metadata_visibility: show corp_creators: Universiti Sains Malaysia. School of Dental Sciences corp_creators: University of Manchester. School of Materials. Manchester Materials Science Centre corp_creators: University of Manchester. School of Materials. Manchester Materials Science Centre corp_creators: University of Manchester. School of Dentistry. Biomaterials Science Unit title: Post-polymerization of dental resin composite evaluated with nanoindentation and micro-Raman spectroscopy ispublished: pub subjects: R full_text_status: public keywords: Nanoindentation, dental composite, Young’s modulus, hardness, degree of conversion note: This article is based on a dissertation submitted to the Manchester Materials Science Centre, UMIST, in partial requirements for the MSc degree. abstract: The aim of the study was to evaluate post-polymerization of resin composite by measuring NanoHardness (H), Young’s Modulus (E) and Degree of Conversion (DC) using nanoindentation and Micro-Raman spectroscopy. For this purpose a computer-controlled NanoIndenter and a Renishaw 1000 Raman Spectrometer fitted with an Olympus microscope attachment, operated at 638 nm, were used. A light- activated resin composite was used in this study, (Z250, 3MESPE). Sub-groups (n=3) of specimens were irradiated for 20, 30, 40 s. All samples for nanoindentation were polished metallographically and typically 50 nano-indentations were performed per specimen. After curing and polishing, half of the samples were tested immediately (Group 1); the others after being stored dry at 37 C for 7 days (Group 2) to allow scope for post-polymerization. H values ranged from 1.08 to 1.40 GPa for Group 1, and from 1.64 to1.71 GPa for Group 2. E values in Group 1 ranged from 19.60 to 19.94 GPa and for Group 2, from 21.42 to 22.05 GPa. DC values ranged from 55 to 66.39%, and 60.90 to 66.47% for Group 1 and Group 2 respectively. All values obtained shown significant different between Groups 1 and 2 (p<0.05); ie as a result of any (further) monomer post- polymerization. The consistently greater H, E and DC values in Group 2 suggest that network stabilization may occur partly by mechanisms supplementary to monomer conversion per se. 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