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Preparation of Chitosan/Poly (vinyl alcohol) Blends Nanofibrous Matrix

机译:壳聚糖/聚乙烯醇共混纳米纤维基质的制备

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摘要

An electrospinning method was used to fabricate chitosan(CS)/ poly(vinyl alcohol) (PVA) blends nanofibrous matrix. The influences of various processing parameters on diameter and morphology of the electrospun nanofibers were investigated by scanning electron microscopy (SEM) technique. The properties of solution with different weight ratio, such as conductivity and viscosity, were measured. The results indicated that the average diameter of the fibers increased with increasing of the concentration and the morphology changed gradually from more beads structure to the uniform fiber-structure with increasing of the concentration of solution from3wt% to 9.5wt%.The diameter of the electrospun fibers decreased with the increasing of CS contents in the blend from 10% to 30%. However, at the blend compositions with above 30% CS, the blend nanofibers were not able to electrospun into the fibrous structure. Higher voltage and larger TCD (tip-to-collector distance) favored the formation of smaller diameter of the electrospun fibers. The Fourier transform infrared (FT-IR) analysis demonstrated that there were strong interactions between CS and PVA molecular resulted from intermolecular hydrogen bonds.
机译:采用静电纺丝法制备了壳聚糖(CS)/聚乙烯醇(PVA)共混纳米纤维基质。通过扫描电子显微镜(SEM)技术研究了各种工艺参数对电纺纳米纤维直径和形貌的影响。测量具有不同重量比的溶液的性质,例如电导率和粘度。结果表明,随着溶液浓度从3wt%增加到9.5wt%,纤维的平均直径随浓度的增加而增加,其形态逐渐从更多的珠状结构变为均匀的纤维结构。随着共混物中CS含量的增加,纤维从10%减少到30%。然而,在具有高于30%的CS的共混物组合物中,共混物纳米纤维不能电纺成纤维结构。较高的电压和较大的TCD(针尖到收集器的距离)有利于形成直径较小的电纺纤维。傅立叶变换红外(FT-IR)分析表明,分子间氢键导致CS与PVA分子之间存在强相互作用。

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