从实验室到中试规模:含导电添加剂的熔融聚丙烯静电纺纳米纤维

K. König, Fabian Langensiepen, G. Seide, Jonas Daenicke, D. Schubert
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引用次数: 7

摘要

在单喷嘴实验室和600喷嘴中试装置上,研究了硬脂酸钠(NaSt)、油酸钠(NaOl)和伊尔斯达特(Irgastat)等导电助剂在熔融电纺丝过程中制备聚丙烯(PP)纳米纤维的可行性。采用高熔体流动指数(MFI=450 ~ 1200 g/10 min)的不同PP等级,添加不同量的添加剂。考察了添加剂对纤维直径、热性能、电导率和聚合物降解性能的影响。在实验室规模上,用PP HL712FB, 4 wt%的NaSt和2 wt%的Irgastat的化合物实现了小于500 nm的纤维直径。实验规模的装置通过加热纺丝室进行扩展,从而影响纤维直径的减小。纳米纤维的制备原则上归因于添加剂的引入提高了导电率。在中试规模下,PP HL508FB和2 wt%的NaSt可获得6.64 μm的最小纤维直径。用单喷嘴生产的纤维和中试规模工厂之间的比较表明,没有进一步的努力就不可能转移结果。由于聚合物在喷嘴内停留时间较长,通过高温粒径排阻色谱可以检测到聚合物有较强的热降解,其中NaOl对热降解的影响最大。高熔体流动PP HL712FB及其化合物由于其低粘度而不能用中试规模装置进行处理,导致喷丝板内建立的压力不足。材料不可纺性的另一个原因是在挤压步骤中由先前的熔体制备引起的较高的热应力和机械应力。进一步调整中试装置是必要的,以确保恒定的温度分布在喷嘴板,以实现均匀的纤维截面。不均匀收集器的实施成功地导致了纤维的均匀沉积,从而获得了各向同性无纺布。
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From Lab to Pilot Scale: Melt Electrospun Nanofibers of Polypropylene with Conductive Additives
In this paper, the feasibility of fabricating polypropylene (PP) nanofibers was investigated using conductive additives such as sodium stearate (NaSt), sodium oleate (NaOl) and Irgastat during melt electro spinning with a single nozzle lab and a 600- nozzle pilot scale device. Varying PP grades of high melt flow indices (MFI=450-1200 g/10 min) were used with different amounts of additives. The effects of the additives on the fiber diameters, thermal properties, electrical conductivity and polymer degradation were investigated. On a lab scale, fiber diameters of less than 500 nm were achieved with the compound of PP HL712FB, 4 wt% NaSt and 2 wt% Irgastat. The lab scale device was extended by a heatable spinning chamber, which affects fiber diameter reduction. The fabrication of nanofibers was in principle attributed to the increase in electrical conductivity with the introduction of the additives. On a pilot scale, the smallest fiber diameter of 6.64 μm could be achieved with PP HL508FB and 2 wt% NaSt. The comparison between the production of the fibers with a single nozzle and the pilot scale plant has revealed that a transfer of results is not possible without further ado. Due to the higher dwell time in the nozzle, a strong thermal degradation of the polymer could be detected with the high temperature size exclusion chromatography, whereby NaOl had the strongest influence on the thermal degradation. The high melt flow PP HL712FB and its compounds could not be processed with the pilot scale device due to its low viscosity, resulting in an insufficient pressure built up within the spinneret. Another reason for the non-spinnability of the material is the higher thermal and mechanical stress caused by the preceding melts preparation in an extrusion step. Further adjustments to the pilot plant are necessary to ensure a constant temperature distribution in the nozzle plate to achieve uniform fiber cross sections. The implementation of an uneven collector has successfully led to an even deposition of the fibers to obtain an isotropic non-woven fabric.
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