结晶
材料科学
过冷
聚乙烯
线性低密度聚乙烯
乙烯
共聚物
等温过程
过饱和度
热力学
化学工程
复合材料
聚合物
化学
有机化学
催化作用
物理
工程类
作者
Evgeny Zhuravlev,Madhavi Vadlamudi,A. Lustiger,René Androsch,Christoph Schick
出处
期刊:ACS Macro Letters
[American Chemical Society]
日期:2016-02-23
卷期号:5 (3): 365-370
被引量:91
标识
DOI:10.1021/acsmacrolett.5b00889
摘要
Extremely fast crystallization of high-density polyethylene and random copolymers of ethylene with up to 16 mol % 1-octene was observed for the first time by ultrafast scanning calorimetry. In order to account for the inherently high crystallization rate of polyethylenes, in nonisothermal and isothermal crystallization experiments cooling rates up to 1 000 000 K/s and crystallization times as short as 10 μs, respectively, were employed. It was possible to supercool the melt of high-density polyethylene down to 57 °C and the melt of a random ethylene/1-octene copolymer with 16 mol % 1-octene down to −33 °C, without prior crystallization. At these temperatures, the characteristic time of the primary crystallization process is of the order of magnitude of 100 μs. Complete vitrification of the liquid would require cooling even faster than 1 000 000 K/s. Compared to the homopolymer, the cooling-rate dependence of the crystallization temperatures and the temperature dependence of the characteristic time of primary crystallization of random ethylene/1-octene copolymers both are nearly parallel shifted to lower temperatures. Fast crystallization under conditions of reduced linear crystal growth rate is possibly caused by boosting homogeneous nuclei density up to 1027 m–3 and urgently requires further investigation.
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