Poly(acrylonitrile-co-butadiene) as polymeric crosslinking accelerator for sulphur network formation

dc.bibliographicCitation.firstPagee04659
dc.bibliographicCitation.issue8
dc.bibliographicCitation.volume6
dc.contributor.authorHait, Sakrit
dc.contributor.authorValentín, Juan López
dc.contributor.authorJiménez, Antonio González
dc.contributor.authorOrtega, Pilar Bernal
dc.contributor.authorGhosh, Anik Kumar
dc.contributor.authorStöckelhuber, Klaus Werner
dc.contributor.authorWießner, Sven
dc.contributor.authorHeinrich, Gert
dc.contributor.authorDas, Amit
dc.date.accessioned2022-12-09T07:11:18Z
dc.date.available2022-12-09T07:11:18Z
dc.date.issued2020
dc.description.abstractThe major controlling factors that determine the various mechanical properties of an elastomer system are type of chemical crosslinking and crosslink density of the polymer network. In this study, a catalytic amount of acrylonitrile butadiene copolymer (NBR) was used as a co-accelerator for the curing of polybutadiene (BR) elastomer. After the addition of this copolymer along with other conventional sulphur ingredients in polybutadiene compounds, a clear and distinct effect on the curing and other physical characteristics was noticed. The crosslinking density of BR was increased, as evidenced by rheometric properties, solid-state NMR and swelling studies. The vulcanization kinetics study revealed a substantial lowering of the activation energy of the sulphur crosslinking process when acrylonitrile butadiene copolymer was used in the formulation. The compounds were also prepared in the presence of carbon black and silica, and it was found that in the carbon black filled system the catalytic effect of the NBR was eminent. The effect was not only reflected in the mechanical performance but also the low-temperature crystallization behavior of BR systems was altered. © 2020 The AuthorsMaterials science; Materials chemistry; Crosslinking accelerator; Sulphur network; Solid state NMR; Curing kinetics; Activation energy; Acrylonitrile butadiene; Polybutadiene; Low-temperature; Crystallization. © 2020 The Authorseng
dc.description.versionpublishedVersion
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/10558
dc.identifier.urihttp://dx.doi.org/10.34657/9594
dc.language.isoeng
dc.publisherLondon [u.a.] : Elsevier
dc.relation.doihttps://doi.org/10.1016/j.heliyon.2020.e04659
dc.relation.essn2405-8440
dc.relation.ispartofseriesHeliyon 6 (2020), Nr. 8eng
dc.rights.licenseCC BY-NC-ND 4.0 Unported
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectAcrylonitrile butadieneeng
dc.subjectActivation energyeng
dc.subjectCrosslinking acceleratoreng
dc.subjectCrystallizationeng
dc.subjectCuring kineticseng
dc.subjectLow-temperatureeng
dc.subjectMaterials chemistryeng
dc.subjectMaterials scienceeng
dc.subjectPolybutadieneeng
dc.subjectSolid state NMReng
dc.subjectSulphur networkeng
dc.subject.ddc540
dc.titlePoly(acrylonitrile-co-butadiene) as polymeric crosslinking accelerator for sulphur network formationeng
dc.typearticle
dc.typeText
dcterms.bibliographicCitation.journalTitleHeliyon
tib.accessRightsopenAccess
wgl.contributorIPF
wgl.subjectChemieger
wgl.typeZeitschriftenartikelger
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