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Crystallinity and microstructure of plasticized poly(vinyl chloride). A 13C and 1H solid state NMR study

机译:增塑聚氯乙烯的结晶度和微观结构。 13C和1H固态NMR研究

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摘要

The combination of 13C solution NMR and 13C solid-state NMR (CP/MAS and MAS) is used to reveal the relative amount of rigid (crystalline) PVC in two PVC/DOP (50/50 wt% of poly(vinyl chloride)/di-2-ethylhexyl phthalate) samples with tacticities, α, of 0.52 and 0.575, respectively. For both samples the crystallinity decreases with increasing temperature, from about 30% at 90 °C to approximately 6% at 180 °C. By means of a careful spectral deconvolution of the 13C solid-state NMR spectra, the relative amounts of different triad sequences in the crystallites of PVC were obtained. The relative fractions of rr and rm sequences, about 0.5 and 0.4 respectively, are found to be constant as a function of temperatures above 90 °C. On the basis of proton low resolution T2 experiments the mean average amorphous chain length between crystals was estimated at 50 monomer units at 160-180 °C. All results can be well understood by assuming the existence of crystallites which on average consist of only a few syndiotactic sequences in the chain direction.
机译:使用13C溶液NMR和13C固态NMR(CP / MAS和MAS)的组合来揭示两种PVC / DOP(50/50 wt%的聚氯乙烯/立构规整度α分别为0.52和0.575的邻苯二甲酸二-2-乙基己酯)。对于两种样品,结晶度均随温度升高而降低,从90°C时的约30%降至180°C时的约6%。通过对13C​​固态NMR光谱进行仔细的光谱去卷积,获得了PVC微晶中不同三单元组序列的相对量。发现rr和rm序列的相对分数分别为约0.5和0.4,是随温度高于90°C而变化的常数。根据质子低分辨率T2实验,在160-180°C下,晶体之间的平均无定形平均链长估计为50个单体单元。假设存在平均在链链方向上仅由几个间同序列组成的微晶,就可以很好地理解所有结果。

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