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dc.contributor.authorAtsushi Katoen_US
dc.contributor.authorToshiya Sudaen_US
dc.contributor.authorYuko Ikedaen_US
dc.contributor.authorShinzo Kohjiyaen_US
dc.contributor.otherNISSAN ARC, LTD.en_US
dc.contributor.otherKyoto Institute of Technologyen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-05-03T08:06:37Z-
dc.date.available2018-05-03T08:06:37Z-
dc.date.issued2011-10-15en_US
dc.identifier.citationJournal of Applied Polymer Science. Vol.122, No.2 (2011), 1300-1315en_US
dc.identifier.issn10974628en_US
dc.identifier.issn00218995en_US
dc.identifier.other2-s2.0-79960088922en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79960088922&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/11690-
dc.description.abstractTo investigate thermal destruction and rearrangement of the carbon black (CB) network consisting of CB aggregates in rubbery matrix, the proper heat-treatment temperature without thermal decomposition of rubber matrix were examined by using differential scanning calorimetry, dynamic mechanical measurements, and thermal expansion measurements. 383 K was chosen as the heat-treatment temperature under vacuum. The volume resistivity (P v ) of 50 phr CB-filled natural rubber vulcanizate (CB-50) increased rapidly up to a heat-treatment time of 24 h and it decreased by further heat-treatment time, whereas the P v of CB-80 remained almost constant without depending on heating time. Three-dimensional electron microscope (3D-TEM) observations revealed that after the heat-treatment for 75 h, the average lengths of the crosslinked and the branched chains and the crosslinked points density (D cross ) of the CB network decreased, whereas the branched points density (D branch ) increased with decrease of D cross . After the heat-treatment, their fractions (F cross ′s) of crosslinked chains decreased, whereas their fractions (F branch ′s) of the branched ones increased. Especially, F branch of CB-50 became larger than that of CB-80, while the decrease of F cross of CB-50 was almost the same as that of CB-80 by the heat-treatment. And, F cross and F branch of the heat-treated CB-50 were the same compositions (F cross and F branch = ca. 0.7 and ca. 0.3, respectively) as those of the heat-treated CB-80. It is suggested that the CB network of CB-80 is more therma l stable than that of CB-50. These results directly indicate that CB network is broken and is rearranged by a heat-treatment. © 2011 Wiley Periodicals, Inc.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=79960088922&origin=inwarden_US
dc.subjectChemistryen_US
dc.subjectMaterials Scienceen_US
dc.titleThermal destruction of carbon black network structure in natural rubber vulcanizateen_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
dc.identifier.doi10.1002/app.33888en_US
Appears in Collections:Scopus 2011-2015

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