کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1886524 1043529 2012 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Physico-chemical transformations in swift heavy ion modified poly(ethyleneterephthalate)
موضوعات مرتبط
مهندسی و علوم پایه فیزیک و نجوم تشعشع
پیش نمایش صفحه اول مقاله
Physico-chemical transformations in swift heavy ion modified poly(ethyleneterephthalate)
چکیده انگلیسی

Thin films of poly(ethyleneterephthalate) (PET) were exposed to different radiation dose brought about by 80 MeV carbon and 98 MeV silicon ion beam. The UV–vis absorption studies reveal that there is decrease in optical band gap energy to the extent of ∼29.3 and 42.1%. The X-ray diffraction analyses have shown that crystallite size decreased by ∼18.6 and 52.6%, indicating amorphization of PET. The colour of PET films change from colourless to light yellowish followed by light brown as radiation dose is increased. The colour formation has been ascribed to an increase in conjugation in the carbon chain. In the case of PET irradiated with carbon ion, the electrical conductivity increased with frequency beyond a threshold value of 1 kHz. The increase in conductivity of PET films on irradiation is due to formation of defects and carbon clusters as a result of polymer chain scission. The thermal study further confirmed the increase in amorphous nature with increase in radiation dose. The results indicate that radiation dose brings about significant physicochemical transformations in PET.


► Thin films of poly(ethyleneterephthalate) exposed to 80 MeV carbon and 98 MeV Silicon ion.
► UV–vis absorption studies reveal decrease of optical energy gap up to ∼29.3 and 42.1%.
► XRD shows 18.6 and 52.6% decrease in crystallite size indicating amorphization of PET film.
► Conductivity measurement with frequency shows a parabolic increase beyond 1 kHz.
► Thermal study confirmed increased amorphous nature of material with radiation dose.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Radiation Physics and Chemistry - Volume 81, Issue 3, March 2012, Pages 284–289
نویسندگان
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