Solid-State Microcellular Polycarbonate Foams. I. The Steady-State Process Space Using Subcritical Carbon Dioxide

被引:31
|
作者
Weller, John E. [1 ]
Kumar, Vipin [1 ]
机构
[1] Univ Washington, Dept Mech Engn, Seattle, WA 98195 USA
来源
POLYMER ENGINEERING AND SCIENCE | 2010年 / 50卷 / 11期
基金
美国国家科学基金会;
关键词
TEMPERATURE; POLYMERS; CO2; POLYSTYRENE; NUCLEATION; DEPENDENCE; PRESSURE; FATIGUE; IMPACT; MODEL;
D O I
10.1002/pen.21736
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The process parameters for production of solid-state microcellular polycarbonate using subcritical CO(2) were explored. Sufficiently long foaming times were used to produce foams, where cell growth had completed, resulting in steady-state structures. A wide range of foaming temperatures and saturation pressures below the critical pressure of CO(2) were investigated, establishing the steady state process space for this polymer-gas system. Processing conditions are presented that produce polycarbonate foams where both the foam density and the average cell size can be controlled. The process space showed that we could produce foams at a constant density, while varying the cell size by and order of magnitude. At a relative density of 0.5, the average cell size could be varied from 4 to 40 mu m. The ability to produce such a family of foams opens the possibility to explore the effect of microstructure, like cell size on the properties of cellular materials. It was found that the minimum foaming temperature for a given concentration of CO(2), determined from the process space, agrees well with the predicted glass transition temperature of the gas-polymer solution. A characterization of the average cell size, cell size distribution, and cell nucleation density for this system is also reported. POLYM. ENG. SCI., 50:2160-2169, 2010. (C) 2010 Society of Plastics Engineers
引用
收藏
页码:2160 / 2169
页数:10
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