Jiao CM, Wang ZZ, Liang XM, Hu Y (2005b) Non-isothermal crystallization kinetics of silane crosslinked polyethylene. Polymer Testing 24(1), 71-80. [In English]

Web link:http://dx.doi.org/10.1016/j.polymertesting.2004.07.007

Keywords:

polyethylene, silane crosslinking, non-isothermal crystallization, crystallization kinetics, low-density polyethylene, ethylene-propylene rubber, ether ketone, ketone), isothermal crystallization, particulate silica, melting, behavior, surface-area, filled ldpe, linking, peroxide

Abstract: The non-isothermal crystallization kinetics of silane crosslinked polyethylene (SXPE) and dicumyl peroxide (DCP) modified polyethylene (DMPE) were studied by differential scanning calorimetry at different cooling rates. Three methods, namely, the Avrami, the Ozawa, and the Mo, were applied to describe the crystallization process of virgin LLDPE, DMPE and SXPE under non-isothermal conditions. The values of half-time of crystallization t(1/2), and the parameter Z(c) in the Avrami method which characterize the kinetics of non-isothermal crystallization, show that the crystallization rates of virgin LLDPE and DMPE are faster than that of SXPE at the same cooling rate, and crystallization rates of all samples increase as the cooling rate increases. The Ozawa model is also suitable to describe the process of the non-isothermal crystallization kinetics of all samples. In the Mo method, it has been found that the F(T) values of virgin LLDPE and DMPE are lower than that of SXPE, meaning that the crystallization rate of virgin LLDPE and DMPE is faster than that of SXPE. (C) 2004 Elsevier Ltd. All rights reserved.