کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
7922711 | 1511801 | 2015 | 6 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Positron annihilation lifetime spectroscopy study on the structural relaxation of phenylmethylsiloxane-modified epoxy hybrids at different aging temperatures
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
مهندسی مواد
مواد الکترونیکی، نوری و مغناطیسی
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چکیده انگلیسی
The cured network conformations and structural relaxation behaviours of the diglycidyl ether of bisphenol A (DGEBA)-methylhexahydrophthalic anhydride (MHHPA) modified with phenylmethylsiloxane-modified epoxy (PMSE) at different aging temperatures were studied using dynamic mechanical analysis (DMA) and positron annihilation lifetime spectroscopy (PALS). The DMA results revealed that the cured PMSE network can insert into the cured DGEBA network to form interpenetrating polymer networks (IPNs). The structural relaxation behaviours of DGEBA-PMSE-0.4 produced using DGEBA, PMSE, and MHHPA at a ratio of 0.6:0.4:1 by equivalent weight were studied using PALS at 150 °C and 55 °C. The aging-induced free volume relaxation parameters of DGEBA-PMSE-0.4 at 150 °C and 55 °C were investigated using the double additive exponential model and the Kohlrausch-Williams-Watts exponential model. For double additive exponential model, only one relaxation time (ζ) of 584.5 h was found at 150 °C; By contrast, there were two separate relaxation times of 37.4 h (ζ1) and 753.6 h (ζ2) at 55 °C. The ζ1 of the IPNs hybrid can be attributed to the network relaxation of PMSE, and the ζ2 can be attributed to the network relaxation of DGEBA at 55 °C. The results suggested the double additive exponential model can effectively predict DGEBA-PMSE hybrid relaxation behaviours.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Materials Chemistry and Physics - Volume 162, 15 July 2015, Pages 82-87
Journal: Materials Chemistry and Physics - Volume 162, 15 July 2015, Pages 82-87
نویسندگان
Chia-Wen Hsu, Chen-Chi M. Ma, Chung-Sung Tan, Hsun-Tien Li,