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dc.contributor.authorWu, Yi-Jhenen_US
dc.contributor.authorChao, Liangen_US
dc.contributor.authorHo, Ko-Shanen_US
dc.contributor.authorHuang, Ying-Jieen_US
dc.contributor.authorHuang, Yu-Lanen_US
dc.contributor.authorYang, Chi-Shiangen_US
dc.contributor.authorTseng, Bo-Haoen_US
dc.date.accessioned2014-12-08T15:22:33Z-
dc.date.available2014-12-08T15:22:33Z-
dc.date.issued2012-06-15en_US
dc.identifier.issn0021-8995en_US
dc.identifier.urihttp://hdl.handle.net/11536/15951-
dc.description.abstractA multiwalled carbon nanotubes (MWCNTs) were carboxylated after refluxing with sulfuric and nitric acids. These attached carboxylic acid groups were further condensated with o-phenylene diamine into amide catalyzed by dicyclohexyl carbodiimide (DCC). The obtained amidized MWCNTs were in situ-polymerized with aniline monomers to graft a conducting polyaniline (PANI) onto MWCNT (ES-g-MWCNTs) through the polymerization occurring in the ortho- and meta-positions. The reduced conductivity of the MWCNT after carboxylation can be recovered after grafting with PANI, which owns a strong ?max at the near infrared region due to the extended conjugation from MWCNTs to PANI. Transmission electronic microscopic pictures show a gradual broadening of the MWCNT diameter after carboxylation, amidization, and polymerization. The weight loss from the thermogravimetric thermograms due to the carboxylations of MWCNTs, amidized MWCNTs, and the PANI grafted MWCNTs into CO2 can be used to estimate the degree of carboxylation, amidization, and grafting of PANI. The degree of carboxylation of MWCNT calculated from ESCA spectrum is around 23% close to that estimated from TGA thermogram. The doping level of redoped PANI-grafted MWCNT is found to be 27.78% much less than the maximum 50% of neat PANI. (c) 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011en_US
dc.language.isoen_USen_US
dc.subjectmultiwalled carbon nanotubeen_US
dc.subjectpolyanilineen_US
dc.subjectconjugationen_US
dc.titleCharacterizations on the amidized multiwalled carbon nanotubes grafted with polyaniline via in situ polymerizationen_US
dc.typeArticleen_US
dc.identifier.journalJOURNAL OF APPLIED POLYMER SCIENCEen_US
dc.citation.volume124en_US
dc.citation.issue6en_US
dc.citation.epage5270en_US
dc.contributor.department材料科學與工程學系奈米科技碩博班zh_TW
dc.contributor.departmentGraduate Program of Nanotechnology , Department of Materials Science and Engineeringen_US
dc.identifier.wosnumberWOS:000301224500104-
dc.citation.woscount2-
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