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dc.contributor.authorKo, J.M.-
dc.contributor.authorRhee, H.W.-
dc.contributor.authorKim, C.Y.-
dc.date.accessioned2024-01-21T23:38:25Z-
dc.date.available2024-01-21T23:38:25Z-
dc.date.created2021-09-02-
dc.date.issued1992-01-
dc.identifier.issn0258-0322-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/146697-
dc.description.abstractThe surface of PPy prepared in a multiple electrolyte solution such as NaDS­NaClO4 in H2O shows a coarser structure than that of the polymer prepared in a single electrolyte system. DS? with a large aliphatic chain is used as a dopant in preparation of PPy. The dopant is trapped in PPy when the polymer is reduced in an aqueous system. A cation Na+ or K+ is inserted into the polymer to balance the free DS? liberated form and remained in it on reduction. PPy doped with DS? shows a high degree of redox reactivity in the system of TBADS­AN but a poor stability in repeated redox process. The degree and rate of redox reactivity enhance when an aqueous solution of NaClO4 is used as an electrolyte system. Both Na+ and ClO4?take part in the redox reaction and the reduction process is intense at only one current potential. Copyright ? 1992 H?thig & Wepf Verlag-
dc.languageEnglish-
dc.titleCompetition between dopants on redox reaction of polypyrrole-
dc.typeArticle-
dc.identifier.doi10.1002/masy.19920530110-
dc.description.journalClass1-
dc.identifier.bibliographicCitationMakromolekulare Chemie. Macromolecular Symposia, v.53, no.1, pp.81 - 88-
dc.citation.titleMakromolekulare Chemie. Macromolecular Symposia-
dc.citation.volume53-
dc.citation.number1-
dc.citation.startPage81-
dc.citation.endPage88-
dc.description.journalRegisteredClassscopus-
dc.identifier.scopusid2-s2.0-84986848046-
dc.type.docTypeArticle-
dc.subject.keywordAuthorpolypyrrole-
dc.subject.keywordAuthorredox reactivity-
dc.subject.keywordAuthorbulky dopant-
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