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dc.contributor.authorRosniza, Hamzah
dc.contributor.authorMohamad, Abu Bakar, Prof.
dc.contributor.authorNik Noriman, Zulkepli, Dr.
dc.contributor.authorMohd Arif Anuar, Mohd Salleh
dc.contributor.authorMohd Mustafa Al-Bakri, Abdullah
dc.date.accessioned2014-03-26T07:21:32Z
dc.date.available2014-03-26T07:21:32Z
dc.date.issued2013
dc.identifier.citationAdvanced Materials Research, vol. 795, 2013, pages 251-255en_US
dc.identifier.isbn978-303785811-0
dc.identifier.issn1022-6680
dc.identifier.urihttp://www.scientific.net/AMR.795.251
dc.identifier.urihttp://dspace.unimap.edu.my:80/dspace/handle/123456789/33142
dc.descriptionLink to publisher's homepage at http://www.ttp.net/en_US
dc.description.abstractA composite comprising cyclopentyl trisilanol siisesquioxanes (CpSSQ(OH)3) and 50% epoxidized natural rubber (ENR-50) was prepared at reflux temperature employed hydrochloric acid (HCl) as catalyst. HCl was found to be an effective catalyst to promote ring opening reaction of ENR-50 and tailored CpSSQ(OH)3 to the ENR-50 polymer chains via chemical reaction. FTIR spectroscopy reveals a hydroxyl stretching indicating the occurrence of epoxide ring opening reaction. !H NMR analysis further proved the incorporation of CpSSQ(OH)3 into ENR-50 polymer chains via shiftment of proton chemical shift and addition in the proton integrals. Si 29NMR analysis evidence the Si-O-C bond through a chemical shift of silanol group from CpSSQ(OH)3.en_US
dc.language.isoenen_US
dc.publisherTrans Tech Publicationsen_US
dc.subjectENR-50en_US
dc.subjectEpoxide ring openingen_US
dc.subjectHybriden_US
dc.subjectSilsequioxanesen_US
dc.titlePreparation of cyciopentyi trisiianoi siisesquioxanes - modified natural rubber (CpSSQ(OH)3 - ENR-50) composite hybrid in the presence of HCI aciden_US
dc.typeArticleen_US
dc.contributor.urlrosniza.hamzah@gmail.comen_US
dc.contributor.urlniknoriman@unimap.edu.myen_US
dc.contributor.urlarifanuar@unimap.edu.myen_US
dc.contributor.urlmustafa_albakri@unimap.edu.myen_US


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