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dc.contributor.authorSasikala, T S-
dc.contributor.authorBindu, P N-
dc.contributor.authorPavithran, C-
dc.contributor.authorSebastian, M T-
dc.date.accessioned2013-06-13T09:46:31Z-
dc.date.available2013-06-13T09:46:31Z-
dc.date.issued2012-06-
dc.identifier.citationLangmuir 28(25):9742-9747;Jun 2012en_US
dc.identifier.urihttp://hdl.handle.net/123456789/454-
dc.description.abstractHybrid silica spheres (HS) of size 270−350 nm with vinyl and aminopropyl surface groups were incorporated in polystyrene (PS),and its effect on dielectric properties, coefficient of thermal expansion(CTE), and strength of PS−HS composite was studied. Incorporation of HS in PS followed a decrease in the dielectric constant from 3.2 for PS to 2.6 for composite with 7.5 vol % HS. The decrease in the dielectric constant was attributed to (i) increased interfacial porosity, (ii) formation of anhydrous HS having low dielectric constant, during hot processing of the composites, and (iii) dispersion and preservation of the anhydrous HS in the hydrophobic matrix. The dielectric constant of the composites with HS content up to 7.5 vol % does not vary much with temperature in the range from −20 to 65 °C. These composites also exhibited reduced CTE and improved flexural strength/stiffness due to good interfacial bonding through HS vinyl groups and dispersion of the filler in the matrix. The dielectric loss increased with HS content, and the loss measured for 7.5 vol % PS−HS composite was 6 × 10−3, as compared to 10−4 for PS. At HS loading above 7.5 vol %, the tendency of HS to agglomerate and form percolated structure lead to an increase in the dielectric constant and decrease in the mechanical properties of the compositesen_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectHybrid silica spheresen_US
dc.subjectPolystyreneen_US
dc.subjectPolyhedral oligomeric silsesquioxaneen_US
dc.subjectBifunctionalizationen_US
dc.titleImproved dielectric and mechanical properties of polystyrene− hybrid silica sphere composite induced through bifunctionalization at the interfaceen_US
dc.typeArticleen_US
Appears in Collections:2012

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