<mets:mets OBJID="oai:myais.fsktm.um.edu.my:1601" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:mods="http://www.loc.gov/mods/v3" LABEL="Eprints Item" xsi:schemaLocation="http://www.loc.gov/METS/ http://www.loc.gov/standards/mets/mets.xsd http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-0.xsd" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mets="http://www.loc.gov/METS/"><mets:metsHdr CREATEDATA="2009-01-09T00:49:52Z"><mets:agent TYPE="ORGANIZATION" ROLE="CUSTODIAN"><mets:name>Malaysian Abstracting and Indexing System</mets:name></mets:agent></mets:metsHdr><mets:dmdSec ID="DMD_oai:myais.fsktm.um.edu.my:1601_mods"><mets:mdWrap MDTYPE="mods"><mets:xmlData><mods:titleInfo><mods:title>Post-polymerization of dental resin composite evaluated with nanoindentation and micro-Raman spectroscopy</mods:title></mods:titleInfo><mods:name type="personal"><mods:namePart type="given"> </mods:namePart><mods:namePart type="family">Mohamad,  D</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given"> </mods:namePart><mods:namePart type="family">Young, R.J. </mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given"> </mods:namePart><mods:namePart type="family">Mann, A.B. </mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given"> </mods:namePart><mods:namePart type="family">Watts, D.C. </mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods: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&lt;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. This could include annealing of the polymer chain segments.</mods:abstract><mods:classification authority="lcc">R Medicine, Dentistry, Pharmacy, Nursing</mods:classification><mods:originInfo><mods:dateIssued encoding="iso8061">2007</mods:dateIssued></mods:originInfo><mods:originInfo><mods:publisher>School of Dental Sciences, Universiti Sains Malaysia</mods:publisher></mods:originInfo><mods:genre>Journal</mods:genre></mets:xmlData></mets:mdWrap></mets:dmdSec><mets:amdSec ID="TMD_oai:myais.fsktm.um.edu.my:1601"><mets:rightsMD ID="rights_oai:myais.fsktm.um.edu.my:1601_mods"><mets:mdWrap MDTYPE="mods"><mets:xmlData><mods:useAndReproduction>
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