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Microcellular Foaming of Polymethylmethacrylate in a Batch Supercritical CO2 Process: Effect of Microstructure on Compression Behavior

机译:分批超临界CO2工艺中聚甲基丙烯酸甲酯的微孔发泡:微观结构对压缩行为的影响。

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摘要

Microcellular foaming of reinforced core/ shell Polymethylmethacrylate (PMMA) was carried out bymeans of supercritical CO2 in a single-step process. Samples were produced using a technique based on the saturation of the polymer under high pressure of CO2(300 bars,40 C), and cellular structure was controlled by varying the depressurization rate from 0.5 bar/s to 1.6 x10-2 bar/sleading to cell sizes from 1lm to 200l m, and densities from 0.8 to 1.0 g/cm3. It was found that the key parameter to control cell size was depressurization rate, and larger depressurization rates generated bigger cell sizes. On the other hand, variation of the density of the samples was not so considerable. Low rate compression tests were carried out, analyzing the dependence of mechanical parameters such as elastic modulus, yield stress and densification strain with cell size. Moreover, the calculation of the energy absorbed for each sample is presented, showing an optimum of energy absorption up to 50% of deformation in the micrometer cellular range (here at a cell size of about 5 µm). To conclude, a brief comparison between neat PMMA and the core/shell reinforced PMMA has been carried out, analyzing the effect of the core/shell particles in the foaming behavior and mechanical properties.
机译:增强核/壳聚甲基丙烯酸甲酯(PMMA)的微孔发泡是通过超临界CO2一步完成的。使用基于聚合物在高压CO2(300 bar,40 C)下的饱和度的技术生产样品,并通过将降压速率从0.5 bar / s更改为1.6 x10-2 bar / s单元尺寸从1lm至200l m,密度从0.8至1.0 g / cm3。发现控制孔尺寸的关键参数是降压速率,而较大的降压速率产生较大的孔尺寸。另一方面,样品密度的变化不是很大。进行了低速压缩试验,分析了机械参数(如弹性模量,屈服应力和致密化应变)与泡孔尺寸的相关性。此外,给出了每个样品吸收能量的计算结果,显示出在微米孔度范围(此处孔度约为5 µm)中,变形率高达50%的最佳能量吸收。总而言之,已经对纯PMMA和核/壳增强的PMMA进行了简要比较,分析了核/壳颗粒对发泡性能和力学性能的影响。

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