Electrospinning of flux‐enhanced chitosan–poly(lactic acid) nanofiber mats as a versatile platform for oil–water separation

Environmentally friendly chitosan (CS)–poly(lactic acid) (PLA) nanofiber mats were designed and constructed by an electrospinning strategy. Studies on the wettability of the CS–PLA nanofiber mats showed that they possessed excellent hydrophobic and oleophilic properties in the pH range 1–12. A layered oil–water mixture was separated by CS–PLA nanofiber mats, and the oil flux of the mats collected by #10 stainless steel wire mesh (sample P‐10) was up to 511.36 L m^?2 h^?1, which was approximately 25 times higher than that of the mats collected by #0 stainless steel wire meshes (sample P‐N). The superior properties of the CS–PLA nanofiber mats may have been due to their tunable porous structure and fine flexibility. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45830.     

CuxS/PAN 3D Nanofiber Mats as Ultra‐Lightweight and Flexible Electromagnetic Interference Shielding Materials

Shielding materials are becoming increasingly important, but present materials suffer from either insufficient mechanical stability or limited shielding properties. In this study, 3D flexible copper sulfide (Cu_xS)/polyacrylonitrile (PAN) nanofiber mats are developed via air spinning followed by chemical reaction with copper salt. The Cu_xS/PAN nanofiber mats exhibit an ultra‐lightweight density of 0.044 g cm^?3 and a thickness of 0.423 mm. Stable electromagnetic interference (EMI) shielding effectiveness (SE) (29–31 dB) of the Cu_xS/PAN composite is achieved in the frequency range of 500–3000 MHz. EMI SE per unit surface density of 16 655.92 dB cm² g^?1 is several orders of magnitude higher than most copper sulfide containing EMI shielding materials reported in literature. In addition, the introduction of the Cu_xS improves the thermal stability and launderability of the PAN mats giving the mats thermal, mechanical, and aqueous stability. Finally, the shielding mechanism of the Cu_xS/PAN nanofiber mats for electromagnetic waves is proposed     

Toughened electrospun nanofibers from crosslinked elastomer‐thermoplastic blends

A crosslink‐able elastomeric polyester urethane (PEU) was blended with a thermoplastic, polyacrylonitrile (PAN), and electrospun into nanofibers. The effects of the PEU/PAN ratio and the crosslinking reaction on the morphology and the tensile properties of the as‐spun fiber mats were investigated. With the same overall polymer concentration (9 wt %), the nanofiber containing higher composition of PEU shows a slight decrease in the average fiber diameter, but the tensile strength, the elongation at break and tensile modulus of the nanofiber mats are all improved. These tensile properties are further enhanced by slight crosslinking of the PEU component within the nanofibers. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Preparation and characterisation of silver‐ or copper‐doped TiO2 catalysts and their catalytic activity in dye degradation

In this study, silver‐ or copper‐doped TiO₂–Ce‐, TiO₂–La‐, and commercial TiO₂ (P25)‐supported catalysts were prepared. The catalysts and supports were characterised by powder X‐ray diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy, and nitrogen adsorption studies. UV‐light‐assisted heterogeneous Fenton‐like oxidation of two different‐structure dyes (anionic azo dye Orange II, CI Acid Orange 7 and cationic triphenylmethane dye Crystal Violet, CI Basic Violet 3) was investigated over the catalysts. Higher catalytic activity was observed in the oxidation of Orange II than in the oxidation of Crystal Violet. For both dyes, the TiO₂–Ce and TiO₂–La‐supported catalysts, which were in the form of anatase only, gave higher photocatalytic activity than the P25‐supported catalysts, which were in the form of anatase and rutile. Complete colour removal was observed during oxidation of Orange II over Cu/TiO₂–Ce and Cu/TiO₂–La catalysts, whereas the highest degree of decolorisation, 89.3%, was achieved by oxidation of Crystal Violet over Ag/TiO₂–Ce. The pH of the solution affected the surface state of the TiO₂, thus affecting the photocatalytic degradation of the dyes. The surface area of the catalysts is also a key parameter that influences their photocatalytic activity. It was observed that catalysts having higher surface areas brought about greater dye degradation.     

Thermal conductivities of electrospun polyimide‐mesophase pitch nanofibers and mats

In this article, we report the preparation and thermal properties of polyimide–mesophase pitch (MP) composite nanofibers and associated nanofiber nonwoven mats produced using an electrospinning process. The addition of MP increased the thermal conductivities of both the individual composite nanofibers and the in‐plane conductivities of the nanofiber mats. The out‐of‐plane conductivity of the mats remained relatively low due to low through thickness connectivity between the nanofibers. These nanofiber mats are flexible and very thin and are good candidates for thermal management films for future flexible electronic devices. POLYM. ENG. SCI., 54:977–983, 2014. © 2013 Society of Plastics Engineers     

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     

Mass‐Production of Electrospun Carbon Nanofiber Containing SiOx for Lithium‐Ion Batteries with Enhanced Capacity

In this study, electrospun carbon nanofibers hybridized with silicon oxide (SiO_x) are prepared by using a syringeless electrospinning system of polyacrylonitrile (PAN) solution containing tetraethylorthosilicate (TEOS) via a sequential pyrolysis process. The syringeless electrospinning system provides a large number of composite nanofibers in a short time, and the obtained composite nanofibers exhibit uniform diameter and morphology. The composite nanofiber is converted into a carbon nanofiber containing SiO_x via a simple pyrolysis. The obtained SiO_x‐carbon nanofiber mat exhibits higher charge/discharge capacity than a general carbon nanofiber, and it provides more stable retention than single crystalline silicon materials. Thus, the mass‐production of a SiO_x‐carbon nanofiber from syringeless electrospinning is a promising method to produce anodic materials for Li‐ion batteries.     

Enhancing water swelling ability and mechanical properties of water‐swellable rubber by PAA/SBS nanofiber mats

Investigation of the potential use of nanofibers to reinforce composites has gained significance in many applications. In this article, the nanofiber mats of poly(acrylic acid) (PAA) and styrene–butadiene–styrene (SBS) triblock copolymer with composites structure were interweaved by double needle electrospinning process. The multiple nanofiber mats were added to conventional water‐swellable rubber (WSR). Improved mechanical and physical properties of WSR were obtained. Enhancement of the swellability of WSR + PAA/SBS nanofiber mats was derived from the PAA constituent absorbing water from the surface into the bulk and introducing random internal water channels between discontinuous superabsorbent polymers. The role of SBS nanofibers in the composite of WSR + PAA/SBS nanofiber mats was more related to the mechanical properties, where the breaking force of the composite increased to twice that of the conventional WSR. Interestingly, after immersion of the WSR + PAA/SBS nanofiber mats in water for 1 week, there was only a slight decrease in their mechanical properties of less than 5% compared to the dry state. The mechanisms and effects of the nanofiber mats in enhancing the mechanical and water swelling properties of WSR are also discussed. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44213.     

Scalable production of polymer nanofiber‐based ropes,cables, and coatings

This article presents a single, scalable manufacturing process for the continuous production of nanofiber‐based ropes, cables, microscale wire coatings, and multimaterial mats. The ropes, cables, and wire coatings were manufactured with a cascading electrospinning setup that was used in conjunction with a rotating ring collector and a take‐up reel. The fibrous mats were realized by replacing the ring collector with a directed nozzle. Both configurations allowed for nanofiber architectures with multiple layers and material combinations. The tensile failure patterns of the cables revealed distinct effects of the multimaterial sheaths. The adhesion strength and load–displacement profiles for the nanofiber coating interfaces were observed to be polymer‐specific. For multimaterial mats, the cospinning of the polymers resulted in a blended mechanical behavior for the composite mats, in contrast to the sequential ply failure observed in laminated mats. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43747.     

Ultrasmall Ag nanocrystals supported on chitosan/PVA nanofiber mats with bifunctional properties

Bifunctional nanofiber mats consisting of chitosan (CS), poly(vinyl alcohol) (PVA), and silver nanocrystals (Ag NCs) have been fabricated by a facile electrospinning method. The formation and presence of Ag NCs supported on CS/PVA nanofibers are confirmed by ultraviolet‐visible spectroscopy and X‐ray diffraction. The morphology of the samples is characterized by transmission electron microscopy and scanning electron microscopy. The prepared Ag NCs/CS/PVA nanofiber mats show pronounced antibacterial activity against Escherichia coli and excellent filtration property for suspended particulate matter (SPM) particles. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46504.     

ZnO nanoparticles dispersed poly(aniline‐co‐o‐anthranilic acid) composites: Photocatalytic reduction of Cr(VI) and Ni(II)

In this report, poly(aniline‐co‐anthranilic acid)/zinc oxide (poly(ANI‐co‐ANA)/ZnO) nanocomposites were prepared by in‐situ chemical oxidative polymerization. Transmission electron microscopy (TEM), X‐ray diffraction, Fourier transform infrared spectroscopy, and ultraviolet–visible spectroscopy measurements were used to characterize the resulting pure copolymer and nanocomposite. TEM analysis showed that the nanoparticles with a mean diameter of 15–25 nm were dispersed in the copolymer matrix. Thermogravimetric analysis indicated that the nanocomposite had a higher decomposition temperature than the pure copolymer. The conductivity measurements showed the resulting nanocomposite possessed higher conductivity as compared to the pure copolymer. Photocatalytic removal of Cr(VI) and Ni(II) from aqueous solution using as‐synthesized nanocomposite under UV‐light irradiation was studied. The reduction patterns of Cr(VI) and Ni(II) were better fitted to first‐order kinetic model. The nanocomposite was also applied as a photocatalyst for the degradation of methylene blue dye. The result revealed substantial degradation of the dye (∼82%) under UV‐light illumination. POLYM. COMPOS., 35:839–846, 2014. © 2013 Society of Plastics Engineers     

Preparation and characterization of a nanofiber mat consisting of Tetra‐PEG prepolymers

Tetra‐PEG gel, which has been known as a mechanically tough and biocompatible gel, was processed into a nanofiber mat by electro‐spinning (ES) and 2‐step treatment process using w/o type emulsion consisted of the Tetra‐PEG prepolymer 1‐octanol/water solution. The 2‐step treatment was carried out in order to increase the cross‐linking points to the as‐spun nanofibers. From this study, we succeeded in insolubilizing poly(ethylene glycol) (PEG) nanofiber, and it was found that the Tetra‐PEG gel nanofiber mat showed high tensile property even at swollen state. The elastic modulus at equilibrium swollen state was 4.5 kPa. In addition, we compared the differences of the structure and tensile property between the Tetra‐PEG nanofiber mat and porous Tetra‐PEG gel prepared by freeze‐dry method. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41353.     

Generation of nanofibers via electrostatic‐Induction‐assisted solution blow spinning

Increasing attention has been given to nanofiber fabrication techniques. Solution blow spinning (SBS) is an innovative, simple, and effective method for producing nanofibers, and it only uses the drawing force of high‐velocity airflow. However, solution‐blown nanofibers easily form bundles; this results in an uneven distribution of nanofibers and an inhomogeneity of nanofiber mats. In this study, electrostatic‐induction‐assisted solution blow spinning (EISBS) was established by the introduction of an additional electrostatic field with an induction circle electrode into the SBS system. The effects of the electrostatic force on the fiber configuration and structure were examined. The results indicate that the electrostatic field effectively separated the fibers. Response surface methodology, based on the four‐factor, three‐level Box–Behnken design, was used to facilitate a more systematic understanding of the processing parameters of EISBS. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42326.     

Crosslinking assisted fabrication of ultrafine poly(vinyl alcohol)/functionalized graphene electrospun nanofibers for crystal violet adsorption

This article reports the fabrication of water‐stable electrospun mats made from water‐soluble poly(vinyl alcohol) and comprising ultrafine nanofibers for a high surface area to volume ratio as required for the adsorption of crystal violet. Acid‐catalyzed crosslinking is uniquely demonstrated as a facile strategy to improve water stability and, just as importantly, fine‐tune the nanofiber size of the electrospun mats. Amine‐functionalized graphene nanoplatelets are incorporated as an adsorption performance enhancer instead of the more widely reported graphene oxide. The functionalized graphene also facilitates fabrication of the composite electrospun mats by direct mixing of the water‐dispersible graphene with the aqueous polymer solution. The enhanced adsorption performance of the polymer nanocomposite mats is explained in detail at the molecular level, while the adsorption mechanism is supported by adsorption isotherm and related kinetic data. Moreover, the adsorbent mats can be removed from the water after use with the mat integrity still maintained. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46318.     

Acid‐dye‐dyeable polyacrylonitrile/ poly(N,N‐dilkylaminoethylacrylate) acrylic blend fiber

An acid‐dye‐dyeable polyacrylonitrile/poly (N,N‐dilkylaminoethylacrylate) blend fiber was prepared. On the basis of research for the dye uptake, color strength, tensile strength, and breaking elongation of the polyacrylonitrile/poly (N,N‐dilkylaminoethylacrylate) blend fiber, it was found that the blend fiber and its fabrics for acid dyes possessed favorable dyeability and mechanical properties. The effect of the polyacrylonitrile ratio on the blend fiber was examined. The optimum dyeing‐process parameters were determined. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Preparation of 3D crimped ZnO/PAN hybrid nanofiber mats with photocatalytic activity and antibacterial properties by blow-spinning

Zinc oxide (ZnO) nanostructures have received widespread attention due to their unique structure and broad application possibilities, but high preparation costs and agglomeration limit their usage. In this article, low-cost and environmentally friendly cellulose and ZnCl₂ are used to synthesize ZnO nanoparticles (ZnO NPs). Subsequently, multifunctional ZnO/polyacrylonitrile hybrid nanofiber mats (ZnO/PAN@NFMs) with mechanical stability suitable for large-scale application are prepared via solution blow-spinning. The synthesized ZnO/PAN@NFMs exhibit higher photodegradation of organic dyes than earlier reported semiconductors and good recycling performance with an organic dye degradation above 94%–98% after five cycles, which is ascribed to fixation of the ZnO NPs in the nanofibers. In addition, the inhibition rate for Escherichia coli and Staphylococcus aureus is above 99.9% and the bacteriostatic rate against E. coli remains as high as 99% after 10 cycles. From these properties, the synthesized composite ZnO/PAN@NFMs are promising for wastewater cleaning and antibacterial fabrics.     

Tautomerism,crystal structure,and copper(II) complexation of isomeric pyridonylazo dyes derived from 2‐ and 4‐aminobenzoic acids

A pair of isomeric aromatic heterocyclic dyes, bearing the same N‐methyl pyridine‐2,6‐dione coupling component but a different 2‐ or 4‐aminobenzoic acid diazo component, were characterised structurally and spectroscopically. X‐ray single‐crystal diffraction analyses revealed that they both adopt the same hydrazone‐tautomeric form and planar molecular conformation between the pyridine and phenyl rings. Furthermore, azo–hydrazone transformation was achieved for the 2‐aminobenzoic‐acid‐based dye after Cu(II) ion complexation, as verified by the formation of a neutral Cu(II) dye–metal complex. The coordination geometry of the central Cu(II) ion exhibits a slightly distorted pyramid with a value of 0.028, where the ligand loses a proton during complexation and serves as the tridentate coordination mode. In addition, thermogravimetric analysis and corresponding differential thermal analysis for the isomeric pair showed that they both have excellent thermal stability, and 4‐aminobenzoic‐acid‐based dye has a higher decomposition temperature (319 °C) than the 2‐aminobenzoic‐acid‐based dye (312 °C). To the best of our knowledge, this is the first structural study on aromatic heterocyclic dyes having aminobenzoic acid and pyridine‐2,6‐dione components at the same time.     

Novel floating photocatalysts based on polyurethane composite foams modified with silver/titanium dioxide/graphene ternary nanoparticles for the visible‐light‐mediated remediation of diesel‐polluted surface water

Photocatalyst loading on a floating substitute is accepted as a promising method for the remediation of diesel‐polluted surface water. Therefore, novel photocatalysts based on polyurethane foams modified with silver/titanium dioxide/graphene ternary nanoparticles (PU–Ag/P25/G) were synthesized and investigated. Scanning electron microscopy, energy‐dispersive X‐ray spectrometry, X‐ray diffraction, Fourier transform infrared spectroscopy, and UV–visible spectroscopy showed the coexistence of Ag, Degussa P25 (P25), and graphene and the nanoscale dispersion of nanoparticles in the matrix and on the surface of the polyurethane (PU) foam. The diesel adsorption capacity of the photocatalyst reached 96 g/g. The maximum diesel degradation was found to be 76% in a period of 16 h. Compared with polyurethane‐foam‐supported P25/graphene (PU–P25/G) and polyurethane‐foam‐supported P25 (PU–P25), all of the adsorption isotherm and degradation kinetics followed the order PU–Ag/P25/G > PU–P25/G > PU–P25 > PU; this was due to the loading of different nanoparticles. Moreover, the degradation efficiency was reduced only 5% after five consecutive reactions; this showed good stability and reusability of the photocatalyst for surface water restoration. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43400.     

In vitro degradation behavior of electrospun polyglycolide,polylactide, and poly(lactide‐co‐glycolide)

The electrospinning of polyglycolide (PGA), poly(L ‐lactide) (PLA), and poly(lactide‐co‐glycolide) (PLGA; L ‐lactide/glycolide = 50/50) was performed with chloroform or 1,1,1,3,3,3‐hexafluoro‐2‐propanol (HFIP) as a spinning solvent to fabricate their nanofiber matrices. The morphology of the electrospun PGA, PLA, and PLGA nanofibers was investigated with scanning electron microscopy (SEM). The PLGA nanofibers, electrospun with a nonpolar chloroform solvent, had a relatively large average diameter (760 nm), and it had a relatively broad distribution in the range of 200–1800 nm. On the other hand, the PGA and PLA fibers, electrospun with a polar HFIP solvent, had a small average diameter (～300 nm) with a narrow distribution. This difference in the fiber diameters may be associated with the polarity of the solvent. Also, the in vitro degradation of PGA, PLA, and PLGA nanofiber matrices was examined in phosphate buffer solutions (pH 7.4) at 37°C. The degradation rates of the nanofiber matrices were fast, in the order of PGA > PLGA ? PLA. Structural and morphological changes during in vitro degradation were investigated with differential scanning calorimetry and wide‐angle X‐ray diffraction. For the PGA matrix, a significant increase in the crystallinity during the early stage was detected, as well as a gradual decrease during the later period, and this indicated that preferential hydrolytic degradation in the amorphous regions occurred with cleavage‐induced crystallization, followed by further degradation in the crystalline region. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 95: 193–200, 2005     

A New Wood Surface Flame‐Retardant Based on Poly‐m‐Aramid Electrospun Nanofibers

Poly(meta‐phenylene isophtalamide) (PMIA) was processed via electrospinning to provide nanofibrous membranes with randomly and aligned fibers. Mechanical performance of such membranes was evaluated, applying a normalization procedure that takes into account the peculiar morphology of such complex substrate where voids can sum up to almost 80% of the sample volume. Random and aligned fibers membranes are applied onto wood panels to test their fire resistance in cone calorimetry when coated in polyaramidic thin nanofiber mats. Tests highlighted that random fibers provide a better fire protection, increasing Time to Ignition and decreasing the Fire Performance Index. Another important parameter affecting the performance is the adhesive system used to apply the nanofibers onto wood that is able to significantly modify the fire performance of the polyaramidic‐coated wood panels. POLYM. ENG. SCI., 59:2541–2549, 2019. © 2019 Society of Plastics Engineers