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Quantifying supercritical CO2 dilation of poly(vinylidene fluoride) and poly(vinylidene fluoride-co-hexafluoro-propylene) utilizing a linear variable differential transducer: Plasticization and melting behavior

机译:使用线性可变差分传感器量化聚偏二氟乙烯和聚偏二氟乙烯-共六氟丙烯的超临界CO2膨胀:塑化和熔融行为

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Melting behavior of semicrystalline poly(vinylidene fluoride) (PVDF) and poly(vinylidene fluoride-co-hexafluoropropylene) is investigated as a function of supercritical CO2 pressure using a Linear Variable Displacement Transformer (LVDT). The melting temperature (T-m) of both polymers is lowered due to supercritical CO2 plasticization. For PVDF, the maximum lowering of T-m (DeltaT(m)=23degreesC) occurs between 483 and 552 bar. The corresponding value for the copolymer is DeltaT(m) = 26degreesC at 552 bar. At higher pressures, hydrostatic effects override plasticization and T-m increases for both polymers. By comparing T-m in N-2, a noninteracting gas, the opposing effects of plasticization and hydrostatic pressure on T-m are explored. [References: 31]
机译:使用线性可变位移变压器(LVDT),研究了超结晶CO2压力对半结晶聚偏二氟乙烯(PVDF)和聚偏二氟乙烯-共六氟丙烯的熔融行为的影响。两种聚合物的熔融温度(T-m)由于超临界CO2塑化而降低。对于PVDF,T-m的最大降低(DeltaT(m)= 23°C)在483和552 bar之间发生。共聚物的相应值为552 bar下的DeltaT(m)= 26℃。在较高的压力下,两种聚合物的静水效应均超过了塑化作用,T-m增加。通过比较非相互作用气体N-2中的T-m,探索了增塑和静水压力对T-m的相反影响。 [参考:31]

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