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Fiber structure development in high-speed melt spinning of poly(ethylene terephthalate-co-ethylene 2,6-naphthalene dicarboxylate)

机译:聚对苯二甲酸乙二醇酯-共-乙烯2,6-萘二羧酸酯的高速熔融纺丝中纤维结构的发展

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摘要

High-speed melt spinning of Poly(ethylene terephthalate-co-ethylene 2,6-naphthalene dicarboxylate) (P(ET/EN)) with EN content of 8% was performed. The structure and mechanical properties of the as-spun fibers thus produced in the take-up velocity range of 0.5 to 7.5 km/min were characterized and compared with those of high-speed spun PET fibers. Molecular orientation increased with an increase in the take-up velocity. The development of molecular orientation of P(ET/EN) was more significant than that of PET at low take-up velocities. Accordingly, orientation-induced crystallization of P(ET/EN) started to occur at a slightly lower take-up velocity compared with PET. On the other hand, the maximum birefringence of P(ET/EN) attained at about 6 km/min was lower than that of PET. Although the crystallization temperature estimated from the thinning behavior of the spinning line is similar, density of P(ET/EN) as-spun fibers obtained at high-speed region was significantly lower than that of PET fibers indicating that the crystallization into PET crystals was suppressed by the addition of EN component to PET.
机译:EN含量为8%的聚对苯二甲酸乙二酯-共-乙烯2,6-萘二甲酸乙二酯(P(ET / EN))进行了高速熔融纺丝。表征了在0.5至7.5 km / min的卷取速度范围内如此生产的初纺纤维的结构和机械性能,并将其与高速纺丝PET纤维进行比较。分子取向随着吸收速度的增加而增加。在低吸收速度下,P(ET / EN)分子取向的发展比PET更为显着。因此,与PET相比,P(ET / EN)的取向诱导结晶开始以稍微更低的吸收速度发生。另一方面,以约6km / min的速度获得的P(ET / EN)的最大双折射低于PET。尽管根据纺丝细化行为估算的结晶温度相似,但在高速区域获得的P(ET / EN)初纺纤维的密度显着低于PET纤维,表明结晶为PET晶体为通过在PET中添加EN成分来抑制。

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