静电纺丝纳米纤维在特殊领域的研究现状和应用

综合阐述了静电纺丝制备纳米纤维的工艺变量以及静电纺丝纳米纤维在特殊领域的研究和应用现状。研究表明:静电纺丝是在静电场作用下将聚合物溶液(或熔体)从喷头喷射出制备纳米纤维的工艺过程,纤维直径从几微米到<100nm,具有独特功能的纳米结构,可广泛应用于导电纤维、生物医用高分子材料等特殊领域。     

静电纺特殊形貌纳米纤维的应用研究进展

特殊形貌的纳米纤维可以通过控制静电纺丝过程工艺及参数条件来制备。特殊形貌的纳米纤维具有比普通纳米纤维更大的比表面积和更高的孔隙率,以及掺杂各类有机/无机材料后赋予纤维的多功能性,使其应用研究已经深入能源环境、催化过滤、生物工程、食品安全等诸多领域,成为纳米材料研究的热点领域之一。但特殊形貌纳米纤维存在研究体系不完善、量产化难度高、重现性差等问题。本文通过对多种特殊形貌纳米纤维的成形机理进行阐述,介绍了特殊形貌纳米纤维独特的形貌结构与性能优势,对其在粒子透过、粒子拦截与传输等领域的应用研究进行了概述。此外,本文对特殊形貌的纳米纤维从研究制备到应用过程中面临的局限性进行了讨论,提出建立完善的特殊形貌纳米纤维研究体系,针对应用领域开发功能性特殊形貌纳米纤维膜,从环保性、稳定性角度出发,推进特殊形貌纳米纤维的产业化发展进程。     

静电纺纳米纤维的应用

综述了静电纺纳米纤维在保护性服用材料、传感器、过滤防护材料、高分子纳米模板、纳米复合改性材料、航空航天等方面的应用;详述了在生物医用材料方面的应用;展望了静电纺丝纳米纤维的发展前景;指出应继续研发具有特殊性能的静电纺纳米纤维新产品,扩大其应用领域,最终实现成果产业化。     

静电纺纳米纤维的研究及应用进展

简述了静电纺丝基本原理及纺丝过程中射流存在的几种不稳定性形式;探讨了静电纺丝制备纳米纤维的主要影响因素。回顾了静电纺丝的发展历程,介绍了纳米纤维在电子器件、生物医学领域、滤材、防护服用材料纤维增强复合材料及传感器感知膜等方面的应用。指出静电纺纳米纤维性能优异、应用广泛,应用于生物医学领域是研发热点,必将进一步产业化。     

静电纺无机纳米纤维的研究进展

综述了静电纺丝制备无机纳米纤维的最新研究进展,主要介绍了电纺氧化物纳米纤维和多组分纳米纤维的研究进展,说明了各种无机纳米纤维的特性、应用前景,并且指出其不足以及今后研究的主要方向.     

静电纺纳米纤维集合体力学性能增强的研究现状

介绍了静电纺纳米单纤维结构调控及静电纺纳米纤维集合体力学性能增强的研究现状,并对今后提高静电纺纳米纤维材料力学性能的研究提出建议.静电纺纳米单纤维结构调控因素包括纺丝溶液性质、纺丝参数、环境因素等.静电纺纳米纤维集合体包括纳米纤维束及纳米纤维膜,纳米纤维束力学性能的增强方法包括热拉伸法、加捻法和化学法,纳米纤维膜力学性...     

不同溶剂对静电纺聚乳酸纳米纤维形态结构的影响

以聚乳酸（PLA）为原料,分别用三种不同的溶剂制得三种纺丝液并采用静电纺丝法,制备了聚乳酸纳米纤维。探讨了溶剂、电压、溶液质量分数对纤维形貌和直径的影响。结果表明,溶剂是决定PLA超细纤维形成的关键因素,三氯甲烷（CHC l3）与二甲基甲酰胺（DMF）混合溶剂（体积比为9∶1）是PLA静电纺丝较为理想的溶剂。在PLA质量分数为6%、极距15 cm、电压25 kV,流量2.5 mL/h的工艺条件下,可制备直径为1 200 nm左右的PLA纤维。     

天然高分子静电纺纳米纤维的研究进展

介绍了静电纺丝的原理及利用静电纺丝方法制备天然高分子纳米纤维的最新研究进展,主要介绍了海藻酸钠、天然纤维素、透明质酸、明胶、胶原蛋白、甲壳素及其衍生物等几种主要的天然高分子静电纺纤维的研究进展,并指出它们在生物医学领域的重要应用。     

静电纺聚乳酸纳米纤维的制备及其孔结构调控

为了调控聚乳酸(PLA)纳米纤维的孔结构,采用静电纺丝技术,以PLA母粒为原料,三氯甲烷(CF)和N,N-二甲基甲酰胺(DMF)按一定比例混合的溶液为溶剂,制备了平均直径在1.37μm的PLA纳米纤维,并对其结构进行表征。结果表明,PLA纳米纤维的平均直径随着纺丝液中CF含量、聚合物浓度、环境湿度的增加而增大;随纺丝电压和灌注速度的增大而呈减小的趋势。同时,环境湿度对纤维表面孔结构有显著影响。随着湿度的增加,纤维表面孔的分布密度增加,且形状由圆形转变为椭圆形。此外,与表面光滑的PLA纳米纤维(2.4 m²/g)相比,所制备的PLA多孔纤维的比表面积提升了10倍(24.0 m²/g)。     

PA6静电纺纳米纤维

讨论了PA6静电纺丝工艺,利用扫描电镜(SEM)观察纤维的形态结构,研究了影响PA6静电纺丝 的因素及其对所形成纤维的形态、直径的影响。结果表明,在甲酸溶液中,PA6质量分数为8％、电压值为15 kV、喷丝头到收集板的垂直距离为20 cm是PA6静电纺丝的最佳工艺条件,可得到直径小于100 nm的PA6 纳米纤维。     

Some fascinating phenomena in electrospinning processes and applications of electrospun nanofibers

Electrospinning has the unique ability to produce ultrathin fibers from a rich variety of materials that include polymers, inorganic or organic compounds and blends. With the enormous increase of research interest in electrospun nanofibers, there is a strong need for a comprehensive review of electrospinning in a systematic fashion. This article presents some fascinating phenomena associated with the remarkable features of nanofibers in electrospinning processes and new progress in applications of electrospun nanofibers. Copyright © 2007 Society of Chemical Industry     

The influence of electrospinning parameters on the structural morphology and diameter of electrospun nanofibers

Electrospinning is a simple method of producing nanofibers by introducing electric field into the polymer solutions. We report an experimental investigation on the influence of processing parameters and solution properties on the structural morphology and average fiber diameter of electrospun poly ethylene oxide (PEO) polymer solution. Experimental trials have been conducted to investigate the effect of solution parameters, such as concentration, molecular weight, addition of polyelectrolyte in PEO solution, solvent effect, as well as governing parameter, such as applied voltage. The concentration of the aqueous PEO solution has shown noteworthy influence on the fiber diameter and structural morphology of electrospun nanofibers. At lower concentrations of PEO polymer solution, the fibers showed irregular morphology with large variations in fiber diameter, whereas at higher concentrations, the nanofibers with regular morphology and on average uniform fiber diameter were obtained. We find that the addition of polyelectrolytes, such as sodium salt of Poly acrylic acid (PAA) and Poly allylamine hydrochloride (PAH), increases the conductivity of PEO solutions and thereby decreases the bead formation in electrospun nanofibers. The increase in applied voltage has been found to affect the structural morphology of nanofiber while the addition of ethanol in PEO solution diminishes the bead defects. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

High performance anti-smog window screens via electrospun nanofibers

Scientific studies clearly link air pollution with adverse effects on human health, which includes reduction of cognitive abilities. Hence quality indoor air is essential in rapidly urbanizing societies. The aim of this research work is to develop anti-smog, air permeable, water-proof, and transparent window screens suitable for natural ventilation. For this purpose, we bonded polyethylene terephthalate (PET) nanofibers on PET grids by electrospinning method with relative near spinning distance. During the process, the incomplete solvent evaporation of the collected jet could enhance the bonding of the PET nanofibers to the PET grids. The experimental results showed that the PET nanofibers had a thick deposition at the yarn edge of the PET grids, which also increased the bonding area between the PET nanofibers and the grids. At the same time, PET nanofibers had a thin deposition between the gaps of the PET grids, which not only increased the number of micron-nano-sized holes but also increased the light transmittance of the window screen. After filtration test for 5 h, the PM2.5 filtration efficiency of this anti-smog window screen was high as to 87% and the PET nanofiber window screen still maintained high light transmittance and superhydrophobicity. This research work is a promising way to prepare anti-smog window screens. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 137, 48657.     

Fabrication and electrical characterization of electrospun polyacrylonitrile‐derived carbon nanofibers

Carbon nanofibers were produced from a polyacrylonitrile/N,N‐dimethylformamide precursor solution by an electrospinning process and later pyrolysis at temperatures ranging from 500 to 1100°C in an N₂ atmosphere for about 1 h. The morphological structure of the nanofibers was studied with scanning electron microscopy. Scanning electron microscopy images of carbonized polyacrylonitrile nanofibers without a gold coating showed that the carbonized polyacrylonitrile nanofibers possessed electrical properties. The thermal behavior of the nanofibers was studied with thermogravimetric analysis. An indirect four‐point‐probe method was used for the measurement of the conductivity of nanofiber mats. The conductivity increased sharply with the pyrolysis temperature. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Pd负载电纺碳纳米纤维的制备及其催化活性

Pd纳米粒子负载的碳纳米纤维是催化Sonogahira偶合反应的良好催化剂,其高长径比使之易于从反应混合物中过滤分离;金属纳米粒子与碳纤维间的强相瓦作用使其具有良好的多次重复使用性.通过电纺丝技术和碳化技术制备了Pd金属纳米粒子负载的电纺碳纳米纤维,透射电镜观察显示最终碳化温度及在该温度下的停留时间是影响钯纳米粒子尺寸及其在纤维中分布的主要因素.并通过所得复合纳米纤维对Sonogahira偶合反应的催化活性研究,发现475～575℃这一温度范围是制备具有良好催化活性的金属钯纳米粒子负载的碳纳米纤维的最佳的碳化温度段.     

Antimicrobial activity of organic photosensitizers embedded in electrospun nylon 6 nanofibers

Nylon 6 nanofibers containing organic photosensitizers were investigated to demonstrate the antimicrobial properties in the application of the material to protective clothing and home appliances. Benzophenone (BP), 4, 4′‐bis(dimethylamino)benzophenone (MK) and thioxanthen‐9‐one (TX) were used as photosensitizers and the nylon 6 nanofibers were prepared using electrospinning. Field emission scanning electron microscopy morphology of the nanofibers showed that even and continuous nylon 6 nanofibers were well prepared through electrospinning and that the organic photosensitizers were evenly distributed in the nanofibers. There was no significant reduction of crystallinity in the nylon 6 nanofibers through the insertion of the organic photosensitizers. After UV (365 nm) irradiation of the photosensitizers, the intensity of peak photon excitation in the electron spin resonance spectra was increased. Antimicrobial properties of the prepared nanofibers were tested against Staphylococcus aureus and Escherichia coli according to JIS Z 2801. It was found that antimicrobial properties of nylon 6 nanofibers containing MK and TX were superior to those of nylon 6 nanofibers containing conventionally used BP. The antimicrobial effects of the nanofibers for S. aureus were superior to those for E. coli. The antimicrobial activity gradually increased as the UV irradiation time increased. Copyright © 2012 Society of Chemical Industry     

静电纺丝制备纳米纤维的进展及应用

简述了静电纺丝的制备原理和影响静电纺丝纤维成形的主要工艺因素;介绍了静电纺丝法制备高分子聚合物、生物大分子、无机物纳米纤维的最新进展,以及这些纳米纤维在过滤、传感器、超疏水性材料、生物医用功能材料、纳米模板等领域的应用;指出静电纺丝制备纳米连续长丝技术亟待发展。     

Oxidative stabilization of pitch-polyacrylonitrile composite nanofibers electrospun by incorporating high-percentage inexpensive pitch

Polyacrylonitrile (PAN)-based composite nanofibers incorporated with high-percentage inexpensive pitch were successfully prepared by a simple electrospinning technique. Low-softening-point naphthalene pitch (NP) has the merit of high solubility but inevitably brings about preoxidation problem. Thus the influence of different preoxidation strategies on the morphology, composition, and structure of composite nanofibers was systematically investigated. The results show that there exists a ternary phase diagram consisting of PAN-pitch-solvent and a suitable apparent viscosity of homogeneous solution, which favors the smooth electrospinning and good adjustment for the diameter of carbon nanofibers (100–500 nm). The crystallinity, crystalline order, and electrical conduction of composite nanofibers are enhanced by incorporating graphitizable NP, for example, the electrical resistance of 50% NP-PAN composite nanofiber films after 800°C carbonization decreases about 30%. Both increasing the oxidation temperature and extending the oxidation time are beneficial to the oxidative stabilization of composite nanofibers with a suitable NP percentage below 50%. Gradient heating (240–340°C) and pressurized (0.08 MPa) preoxidations could accelerate the oxidative stabilization of composite nanofibers with a high NP percentage up to 110% and significantly shorten the oxidation time by half. Therefore, this study paves the road for facile preparation of cost-competitive carbon nanofibers with controllable morphology, structure, and properties.