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Electrospinning and Carbonization of Emulsion Polymerized polyacrylonitrile

机译:乳液聚合聚丙烯腈的静电纺丝和碳化

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Polyacrylonitrile (PAN) nanoparticles in sizes ranging from approximately 100 to 500 nm were prepared by emulsion polymerization of acrylonitrile in a continuous aqueous phase in the presence of potassium persulfate (KPS) as initiator and sulfonate surfactants (SDS). The influence of various polymerization parameters (e.g., concentration of monomer and initiator, type and concentration of surfactant and solvent, temperature and time of polymerization) on the properties (e.g., size and size distribution, average molecular weight, etc.) of the particles has been investigated. The polymerization of acrylonitrile can occur within the surfactant micelles. A discussion concerning the role of this mechanism under different conditions, including comparison with previous literature, is also presented. The synthesized PAN as a precursor of carbon fibers with diameters in the range 100-400 nm were obtained by electric-spinning of PAN/DMF solution. The higher average molecular weight PAN was, the better uniform diameters of electrospun nanofiber webs were.
机译:在过硫酸钾(KPS)作为引发剂和磺酸盐表面活性剂(SDS)的存在下,通过丙烯腈在连续水相中的乳液聚合,制备了尺寸范围约为100至500 nm的聚丙烯腈(PAN)纳米粒子。各种聚合参数(例如单体和引发剂的浓度,表面活性剂和溶剂的类型和浓度,聚合的温度和时间)对颗粒性质(例如大小和尺寸分布,平均分子量等)的影响已被调查。丙烯腈的聚合可以在表面活性剂胶束内发生。还讨论了该机制在不同条件下的作用,包括与以前的文献进行了比较。通过电纺PAN / DMF溶液获得直径为100-400nm的作为碳纤维前体的合成PAN。 PAN的平均分子量越高,电纺纳米纤维网的均匀直径越好。

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