Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/91720
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dc.titleStructures and properties of chemically reduced polyanilines
dc.contributor.authorZeng, X.-R.
dc.contributor.authorKo, T.-M.
dc.date.accessioned2014-10-09T08:21:25Z
dc.date.available2014-10-09T08:21:25Z
dc.date.issued1998-03
dc.identifier.citationZeng, X.-R.,Ko, T.-M. (1998-03). Structures and properties of chemically reduced polyanilines. Polymer 39 (5) : 1187-1195. ScholarBank@NUS Repository.
dc.identifier.issn00323861
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/91720
dc.description.abstractHCl-doped emeraldine form of polyaniline (PANI-H) was synthesized by oxidative polymerization of aniline in aqueous hydrochloric acid solution using potassium dichromate as an oxidant. The undoped form of PANI-H (i.e. PANI) was chemically reduced using hydrazine as the reductant. The structure, doping, conductivity and thermal stability of the reduced polyaniline (PANI-R) were studied by elemental analysis, FT-i.r., solid-state 13C-NMR, XPS and TGA. It was found that most of the quinoid structural units in PANI were reduced to benzenoid structural units. PANI-R had been doped with HCl and iodine, but only the iodine-doped product (PANI-RI) showed high electrical conductivity. FT-i.r. and XPS results indicated that some of the benzenoid structural units in PANI-R were oxidized to quinoid structural units during the iodine-doping process and a highly conjugated π system might be formed in the PANI-RI molecular chains. TGA results indicated that PANI-R had better thermal stability than PANI. The dopants - HCl and iodine - were almost completely removed from the HCl and iodine-doped polyanilines below 250°C. PANI-R could also be oxidized by potassium dichromate. The thermal stability of the intrinsically oxidized PANI-R (PANI-RO) was unexpectedly poor. The electrical conductivity of HCl-doped PANI-RO was much lower than that of HCl-doped PANI. © 1997 Elsevier Science Ltd. All rights reserved.
dc.sourceScopus
dc.subjectChemical reduction
dc.subjectConducting polymer
dc.subjectPolyaniline
dc.typeArticle
dc.contributor.departmentCHEMICAL ENGINEERING
dc.description.sourcetitlePolymer
dc.description.volume39
dc.description.issue5
dc.description.page1187-1195
dc.description.codenPOLMA
dc.identifier.isiutNOT_IN_WOS
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