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Synthesis, characterization and ESR study of the gamma-radiolysis of aromatic polyesters containing isomeric naphthalene links

Authors
Hill, DJTChoi, BKAhn, HKChoi, EJ
Issue Date
Oct-1999
Publisher
WILEY-BLACKWELL
Keywords
aromatic polyesters; synthesis; thermal properties; sensitivity to gamma-radiolysis
Citation
POLYMER INTERNATIONAL, v.48, no.10, pp 956 - 962
Pages
7
Journal Title
POLYMER INTERNATIONAL
Volume
48
Number
10
Start Page
956
End Page
962
URI
https://scholarworks.bwise.kr/kumoh/handle/2020.sw.kumoh/27068
DOI
10.1002/(SICI)1097-0126(199910)48:10<956::AID-PI254>3.0.CO;2-N
ISSN
0959-8103
1097-0126
Abstract
Six polyesters were synthesized from 4,4'-(hexafluoroisopropylidene) -bis(benzoyl chloride) and 1,4-, 1,5-, 1,6-, 2,3-, 2,6- and 2,7-naphthalene diol (ND) isomers. The structures of the polyesters were characterized by IR spectroscopy and the results were in good agreement with the expected structures. Inherent viscosities of tetrachloroethane, (TCE) solutions at 303K ranged from 0.11 to 0.46 dlg(-1) The glass transition temperatures were found to be in the range 425-494 K by DSC thermal analysis. Thermogravimetric analyses showed two-stage weight losses and revealed the excellent thermal stability of the polymers. All the polyesters were irradiated in an AECL Gammacell 220 unit at a dose rare of approximately 6.7 kGy h(-1) to doses in the range 0-15 kGy at 77 K and 300 K. The G values for radical formation in the polyesters were found to be in the range 0.41-0.81 at 77 K and 0.56-1.49 at 300 K. At 77 K up to 15% of the radicals formed on radiolysis were found to be anionic. Annealing experiments were carried out to identify the neutral radicals, which were assigned Co phenyl, benzoyl and phenoxyl radicals. (C) 1999 Society of Chemical Industry.
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