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首页> 外文期刊>Journal of Polymer Research >Effect of temperature on thermal, mechanical and morphological properties of polypropylene foams prepared by single step and two step batch foaming process
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Effect of temperature on thermal, mechanical and morphological properties of polypropylene foams prepared by single step and two step batch foaming process

机译:温度对单步制备的聚丙烯泡沫热,机械和形态学性能的影响及两步批量发泡工艺

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This study reports the influence of foaming temperature on morphological and thermo-mechanical characteristics of polypropylene (PP) foams prepared using two different methods of batch foaming at low saturation pressures. In the first method, involving single-step pressure-induced-foaming (PIF), the solid specimen was heated to different temperatures in a high-pressure vessel, and then saturated CO2 under pressure. Depressurization then led to foaming. In the second method, involving a two-step temperature-induced-foaming (TIF), the solid specimen was saturated with pressurized CO2 at room temperature for a specific period of time and then the CO2 laden specimen was immersed in hot glycerol bath at different temperatures for foaming. SEM micrographs of the fractured foamed specimens were employed for measurement of cell-size distribution. The average cell sizes ranged between 3 and 310m in specimens obtained using PIF, while in case of foams prepared by TIF, the cell sizes ranged between 30 and 70m. The cell sizes achieved in TIF are significantly smaller and more uniform as compared to those in PIF foams. The density (0.393-0.186gcm(-3)) of PIF foams was seen to decrease with increasing foaming temperature; in contrast, in case of TIF the density remained more or less unchanged around 0.43-0.47gcm(-3) with changes in foaming temperature. The foamed specimens were characterized in uniaxial compression; the stiffness (elastic and collapse moduli) and compressive strengths of both the PIF and TIF foams were seen to decrease with increase in cell-size. The magnitude of plateau-regime stresses within the compressive stress-strain response showed strong correlation with the foam cell-wall thickness. The crystallinity of the foamed specimens was observed to decrease with increase in foaming temperatures. The thermal stability of both PIF and TIF foams in general showed improvement compared with the PP matrix.
机译:本研究报告了发泡温度对使用两种不同的批量发泡方法在低饱和压力下制备的聚丙烯(PP)泡沫的形态学和热机械特性的影响。在第一种方法中,涉及单步压诱导的发泡(PIF),将固体样品加热到高压容器中的不同温度,然后在压力下饱和CO 2。减压然后导致发泡。在第二种方法中,涉及两步温度诱导的发泡(TIF),固体样品在室温下在室温下在室温下饱和,然后将CO 2载载样品浸入不同的甘油浴中泡沫的温度。用于测量细胞尺寸分布的裂缝泡沫样品的SEM显微照片。在使用PIF获得的样品中的平均电池尺寸范围为3至310m,而在通过TIF制备的泡沫的情况下,电池尺寸在30至70m之间。与PIF泡沫中的那些相比,TIF中实现的细胞尺寸明显较小且更均匀。 PIF泡沫的密度(0.393-0.186cm(-3))被认为随着发泡温度的增加而降低;相反,在TIF的情况下,在发泡温度的变化,密度大约0.43-0.47gcm(-3)左右保持不变。泡沫样品的特征在于单轴压缩; PIF和TIF泡沫的刚度(弹性和塌陷模量)和抗压强度被认为随着细胞尺寸的增加而降低。压缩应力 - 应变响应内的高原调节应力的大小表现出与泡沫细胞壁厚的强相关性。观察到泡沫样品的结晶度随着发泡温度的增加而降低。与PP基质相比,PIF和TIF泡沫的热稳定性显示出改善。

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