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Hypothesis: Nanocellulose and nanochitin are both biobased materials with complementary structures and properties. Both exhibit pH-dependent surface charges which are opposite in sign. Hence, it should be possible to manipulate them to form complexed structures via ionic bond formation at prescribed pH conditions., Experiment: Nanocellulose and nanochitin were mixed after exposure to acidic or neutral conditions to influence their ionization state. The heat of interaction during the introduction of nanochitin to nanocellulose was monitored via isothermal titration calorimetry. The strength and gel properties of the resulting structures were characterized via rheological measurement., Findings: The resultant gel properties in the designed hybrid systems were found to depend directly on the charge state of the starting materials, which was dictated by pH adjustment. Different interparticle interactions including ionic attraction, hydrophobic associations, and physical entanglement were identified in the systems and the influence of each was elucidated for different conditions of pH, concentration, and ratio of nanochitin to nanocellulose. Hydrophobic associations between neutralized nanochitin particles were found to contribute strongly to increased elastic modulus values. Ionic complex formation was found to provide enhanced stability under broader pH conditions, while physical entanglement of cellulose nanofibers was a substantial thickening mechanism in all systems., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier Inc. All rights reserved.)

Heterogeneous acetylation of wood fibers is proposed for weakening their interfibrillar hydrogen bonding, which facilitates their processing into micro- and nanocelluloses that can be further used to synthesize filaments via wet-spinning. The structural (SEM, WAXD), molecular (SEC), and chemical (FTIR, titration) properties of the system are used to propose the associated reaction mechanism. Unlike the homogeneous acetylation, this method does not alter the main morphological features of cellulose fibrils. Thus, we show for the first time, the exploitation of synergies of compositions simultaneously comprising dissolved cellulose esters and suspended cellulose micro- and nanofibrils. Such colloidal suspension forms a co-continuous assembly with a matrix that interacts strongly with the micro- and nanofibrils in the dispersed phase. This facilitates uninterrupted and defect-free wet-spinning. Upon contact with an antisolvent (water), filaments are easily formed and display a set of properties that set them apart from those reported so far for nanocelluloses: a remarkable stretchability (30% strain) and ultrahigh toughness (33 MJ/m 3 ), both surpassing the values of all reported nanocellulose-based filaments. All the while, they also exhibit competitive stiffness and strength (6 GPa and 143 MPa, respectively). Most remarkably, they retain 90% of these properties after long-term immersion in water, solving the main challenge of the lack of wet strength that is otherwise observed for filaments synthesized from nanocelluloses.

Fumed silica (FS) particles with hydrophobic (R805) or hydrophilic (A150) surface functionalities are incorporated in polyacrylonitrile (PAN) fibers by electrospinning to produce mats with controlled wettability. Rheological measurements are conducted to elucidate the particle-polymer interactions and characterize the system while microscopic and analytic tools are used to examine FS location within both fibers and films to aid in the fundamental understanding of wetting behavior. Unlike traditional polymers, we find these systems to be gel-like, yet electrospinnable; the fumed silica networks break down into smaller aggregates during the electrospinning process and disperse both within and on the surface of the fibers. Composite nanofiber mats containing R805 FS exhibit an apparent contact angle over 130° and remain hydrophobic over 30 min, while similar mats with A150 display rapid surface-wetting with a static contact angle of ∼30°. Wicking experiments reveal that the water absorption properties can be further manipulated, with R805 FS-impregnated mats taking up only 8% water relative to mat weight in 15 min. In contrast, PAN fibers containing A150 FS absorb 425% of water in the same period, even more than the pure PAN fiber (371%). The vastly different responses to water demonstrate the versatility of FS in surface modification, especially for submicron fibrous mats. The role of fumed silica in controlling wettability is discussed in terms of their surface functionality, placement on nanofibers and induced surface roughness.

We report an enzyme immobilization method effective at elevated temperatures (up to 105 °C) and sufficiently robust for hyperthermophilic enzymes. Using a model hyperthermophilic enzyme, α-galactosidase from Thermotoga maritima, immobilization within chemically cross-linked poly(vinyl alcohol) (PVA) nanofibers to provide high specific surface area is achieved by (1) electrospinning a blend of a PVA and enzyme and (2) chemically cross-linking the polymer to entrap the enzyme within a water insoluble PVA fiber. The resulting enzyme-loaded nanofibers are water-insoluble at elevated temperatures, and enzyme leaching is not observed, indicating that the cross-linking effectively immobilizes the enzyme within the fibers. Upon immobilization, the enzyme retains its hyperthermophilic nature and shows improved thermal stability indicated by a 5.5-fold increase in apparent half-life at 90 °C, but with a significant decrease in apparent activity. The loss in apparent activity is attributed to enzyme deactivation and mass transfer limitations. Improvements in the apparent activity can be achieved by incorporating a cryoprotectant during immobilization to prevent enzyme deactivation. For example, immobilization in the presence of trehalose improved the apparent activity by 10-fold. Minimizing the mat thickness to reduce interfiber diffusion was a simple and effective method to further improve the performance of the immobilized enzyme.

We investigate the immobilization of a model system of functionalized yeast that surface-display enhanced green fluorescent protein (eGFP) within chemically crosslinked polyvinyl alcohol (PVA) nanofibers. Yeast is incorporated into water insoluble nanofibrous materials by direct electrospinning with PVA followed by vapor phase chemical crosslinking of the polymer. Incorporation of yeast into the fibers is confirmed by elemental analysis and the viability is indicated by live/dead staining. Following electrospinning and crosslinking, we confirm that the yeast maintains its viability as well as the ability to express eGFP in the correct conformation. This method of processing functionalized yeast may thus be a powerful tool in the direct immobilization of properly folded, active enzymes within electrospun nanofibers with potential applications in biocatalysis.

We report on the synthesis of tuned energy band gap Mg(x)Zn(1-x)O nanofibers (NFs) with different Mg(2+) content via the sol-gel electrospinning (ES) technique wherein the addition of the doping material affects not only the morphologies of as-spun ZnAc/PVA and MgAc/ZnAc/PVA nanofibers but also the crystal microstructure and optical properties of calcined ZnO and Mg(x)Zn(1-x)O nanofibers. Following an appropriate aqueous solution preparation of magnesium acetate (MgAc) and zinc acetate (ZnAc) with poly(vinyl alcohol) (PVA), electrospinning is performed and then as-spun nanofibers are calcined in an air atmosphere at 600 °C for 3 h. As-spun and calcined nanofiber diameters and morphologies are evaluated with scanning (SEM) and transmission (TEM) electron microscopies, whereas crystalline microstructural interpretations of ZnO and Mg(x)Zn(1-x)O are conducted with wide-angle X-ray diffraction spectra (XRD). Surface chemical composition and elemental evaluation of calcined nanofibers are examined with X-ray photoelectron spectroscopy (XPS), and optical properties and crystal defect analyses of the calcined nanofibers are conducted with photoluminescence spectra (PL). We observe a sharp reduction in fiber diameter upon calcination as a result of the removal of organic species from the fibers and conversion of ceramic precursors into ceramic nanofibers, and the appearance of a range of fiber morphologies from "bead in a string" to "sesame seed" coverage depending on fiber composition. Because Zn(2+) and Mg(2+) have similar ionicity and atomic radii, some Zn(2+) atoms are replaced by Mg(2+) atoms in the crystals, leading to a change in the properties of crystal lattices. The band gap energy of the calcined fibers increases significantly with addition of Mg(2+) along with an increase in the ultraviolet (UV) photoluminescence emission of the fibers.

We report on the microstructural crystal phase transformation of electrospun TiO(2) nanofibers generated via sol-gel electrospinning technique, and the incorporation of as-synthesized CdSe quantum dots (QDs) to different phases of TiO(2) nanofibers (NFs) via bifunctional surface modification. The effect of different phases of TiO(2) on photo-excited electron injection from CdSe QDs to TiO(2) NFs, as measured by photoluminescence spectroscopy (PL) is also discussed. Nanofiber diameter and crystal structures are dramatically affected by different calcination temperatures due to removal of polymer carrier, conversion of ceramic precursor into ceramic nanofibers, and formation of different TiO(2) phases in the fibers. At a low calcination temperature of 400 (o)C only anatase TiO(2) nanofiber are obtained; with increasing calcination temperature (up to 500 (o)C) these anatase crystals became larger. Crystal transformation from the anatase to the rutile phase is observed above 500(o)C, with most of the crystals transforming into the rutile phase at 800(o)C. Bi-functional surface modification of calcined TiO(2) nanofibers with 3-mercaptopropionic acid (3-MPA) is used to incorporate as-synthesized CdSe QD nanoparticles on to TiO(2) nanofibers. Evidence of formation of CdSe/TiO(2) composite nanofibers is obtained from elemental analysis using Energy Dispersive X-ray spectroscopy (EDS) and TEM microscopy that reveal templated quantum dots on TiO(2) nanofibers. Photoluminescence emission intensities increase considerably with the addition of QDs to all TiO(2) nanofiber samples, with fibers containing small amount of rutile crystals with anatase crystals showing the most enhanced effect.

The formation of 3D electrospun mat structures from alginate-polyethylene oxide (PEO) solution blends is reported. These unique architectures expand the capabilities of traditional electrospun mats for applications such as regenerative medicine, where a scaffold can help to promote tissue growth in three dimensions. The mat structures extend off the surface of the flat collector plate without the need of any modifications in the electrospinning apparatus, are self-supported when the electric field is removed, and are composed of bundles of nanofibers. A mechanism for the unique formations is proposed, based on the fiber-fiber repulsions from surface charges on the negatively charged alginate. Furthermore, the role of the electric field in the distribution of alginate within the nanofibers is discussed. X-ray photoelectron spectroscopy is used to analyze the surface composition of the electrospun nanofiber mats and the data is related to cast films made in the absence of the electric field. Further techniques to tailor the 3D architecture and nanofiber morphology by changing the surface tension and relative humidity are also discussed., (Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

We examine the protein distribution within an electrospun polymer nanofiber using polyvinyl alcohol and bovine serum albumin as a model system. We hypothesize that the location of the protein within the nanofiber can be controlled by carefully selecting the pH and the applied polarity of the electric field as the pH affects the net charge on the proteins. Using fluorescently labeled BSA and surface analysis, we observe that the distribution of BSA is affected by the pH of the electrospinning solution. Therefore, we further probe the relevant forces on the protein in solution during electrospinning. The role of hydrodynamic friction was assessed using glutaraldehyde and HCl as a tool to modify the viscosity of the solution during electrospinning. By varying the pH and the polarity of the applied electric field, we evaluated the effects of electrostatic forces and dielectrophoresis on the protein during fiber formation. We surmise that electrostatic forces and hydrodynamic friction are insignificant relative to dielectrophoretic forces; therefore, it is possible to separate species in a blend using polarizability contrast. A coaxial distribution of protein in the core can be obtained by electrospinning at the isoelectric point of the protein, whereas surface enrichment can be obtained when the protein carries a net charge.

Composite carbon-tin oxide (C-SnO(2)) nanofibers are prepared by two methods and evaluated as anodes in lithium-ion battery half cells. Such an approach complements the long cycle life of carbon with the high lithium storage capacity of tin oxide. In addition, the high surface-to-volume ratio of the nanofibers improves the accessibility for lithium intercalation as compared to graphite-based anodes, while eliminating the need for binders or conductive additives. The composite nanofibrous anodes have first discharge capacities of 788 mAh g(-1) at 50 mA g(-1) current density, which are greater than pure carbon nanofiber anodes, as well as the theoretical capacity of graphite (372 mAh g(-1)), the traditional anode material. In the first protocol to fabricate the C-SnO(2) composites, tin sulfate is directly incorporated within polyacrylonitrile (PAN) nanofibers by electrospinning. During a thermal treatment the tin salt is converted to tin oxide and the polymer is carbonized, yielding carbon-SnO(2) nanofibers. In the second approach, we soak the nanofiber mats in tin sulfate solutions prior to the final thermal treatment, thereby loading the outer surfaces with SnO(2) nanoparticles and raising the tin content from 1.9 to 8.6 wt %. Energy-dispersive spectroscopy and X-ray diffraction analyses confirm the formation of conversion of tin sulfate to tin oxide. Furthermore, analysis with Raman spectroscopy reveals that the additional salt soak treatment from the second fabrication approach increases in the disorder of the carbon structure, as compared to the first approach. We also discuss the performance of our C-SnO(2) compared with its theoretical capacity and other nanofiber electrode composites previously reported in the literature.

Electrospun natural biopolymers are of great interest in the field of regenerative medicine due to their unique structure, biocompatibility, and potential to support controlled release of bioactive agents and/or the growth of cells near a site of interest. The ability to electrospin chitosan and alginate to form polyionic complexed nanofibrous scaffolds was investigated. These nanofibers crosslink in situ during the electrospinning process, and thus do not require an additional chemical crosslinking step. Although poly(ethylene oxide) (PEO) is required for the electrospinning, it can be subsequently removed from the nanofibers simply by incubating in water for a few days, as confirmed by attenuated total reflectance Fourier transform infrared. Solutions that allowed uniform nanofiber formation were found to have viscosities in the range of 0.15-0.7 Pa·s and conductivities below 4 mS/cm for chitosan-PEO and below 2.2 mS/cm for alginate-PEO. The resultant nanofibers both before and after PEO extraction were found to be uniform and on the order of 100 nm as determined by scanning electron microscopy. The dynamic rheological properties of the polymer mixtures during gelation indicated that the hydrogel mixtures with low storage moduli provided uniform nanofiber formation without beaded structures. Increased amounts of chitosan in the PEO-extracted chitosan-alginate nanofibers resulted in a lower swelling ratio. Additionally, these nanofibrous scaffolds exhibit increased cell adhesion and proliferation compared to those made of alginate alone, due to the presence of the chitosan, which promotes the adsorption of serum proteins. Thus, these nanofibrous scaffolds formed purely via ionic complexation without toxic crosslinking agents have great potential for guiding cell behavior in tissue regeneration applications.

Alginate, a natural polysaccharide that has shown great potential as a cell scaffold for the regeneration of many tissues, has only been nominally explored as an electrospun biomaterial due to cytotoxic chemicals that have typically been used during nanofiber formation and crosslinking. Alginate cannot be electrospun by itself and is often co-spun with poly(ethylene oxide) (PEO). In this work, a cell adhesive peptide (GRGDSP) modified alginate (RA) and unmodified alginate (UA) were blended with PEO at different concentrations and blending ratios, and then electrospun to prepare uniform nanofibers. The ability of electrospun RA scaffolds to support human dermal fibroblast cell attachment, spreading, and subsequent proliferation was greatly enhanced on the adhesion ligand-modified nanofibers, demonstrating the promise of this electrospun polysaccharide material with defined nanoscale architecture and cell adhesive properties for tissue regeneration applications.

Electrospun poly (vinyl alcohol) nanofibers are coated with aluminum oxide using atomic layer deposition (ALD) to control the dissolution rate of the nanofiber mats in high-humidity and aqueous environments. In this regard, ALD offers an effective method to provide a robust, conformal coating to the entire nanofiber surface without modifying the core material. The thickness of the coating, controlled by varying the number of ALD cycles from 2 to 200, enables tuning of the nanofiber stability in water from a few seconds for an uncoated sample to over 5 weeks for a 200 cycle coated sample. Changing the rate of nanofiber dissolution modulates the release of embedded small molecules within the polymer matrix from minutes to weeks while minimizing the 'burst' effect typically associated with nanoscale systems. This simple nanofiber coating technique shows great potential as a method to tune shelf-life, mat degradation, and small molecule release from highly water-soluble polymers, hitherto unexplored, in a wide range of fields, including biomedical, agricultural, and packaging. [ABSTRACT FROM AUTHOR]

A multiple jet, needle-less process to fabricate electrospun nanofibers from foamed columns, produced by injecting compressed gas through a porous surface into polymer solutions, capable of circumventing syringe electrospinning shortcomings such as needle clogging and restrictions in production rate is presented. Using polyvinyl alcohol and polyethylene oxide (PEO) as model systems, we identify key design, processing, and solution parameters for producing uniform fibers. Increasing electrode surface area produces thicker mats, suggesting charge distribution through the bulk foam facilitates electrospinning. Similar trends between foam and syringe electrospinning are observed for collection distance, electric field strength, and polymer concentration. Interestingly, the empirical correlation between polymer entanglement and fiber formation are found to be similar for both foam and traditional needle electrospinning, but the fiber crystallinity shows enhancement with foam electrospinning. In addition, foam electrospinning with a PEO-nonionic surfactant system yields two orders of magnitude increase in production rate compared to syringe electrospinning. © 2014 American Institute of Chemical Engineers AIChE J, 60: 1355-1364, 2014 [ABSTRACT FROM AUTHOR]

ABSTRACT In this study, the influence of surfactants on the processability of electrospun polyacrylonitrile (PAN) nanofibers and their carbonized analogs was investigated. The surfactants employed in this effort are Triton X-100 (nonionic surfactant, SF-N), sodium dodecyl sulfate (SDS) (anionic surfactant, SF-A), and hexadecyltrimethylammonium bromide (HDTMAB) (cationic surfactant, SF-C). Interactions between electrospun PAN and the surfactants, reflected in effects on as-spun and carbonized nanofiber morphologies and microstructures, were explored. The results show that uniform nanofibers are obtained when cationic and anionic surfactants (surfactant free and nonionic surfactants) are utilized in the preparation of electrospun PAN. In contrast, a bead-on-a-string morphology results when the aniconic and cationic surfactants are present, and defect structure is enhanced with cationic surfactant addition. Moreover, fiber breakage is observed when the nonionic surfactant Triton X-100 is employed for electrospinning. After carbonizaition, the PAN polymers were observed to have less ordered structures with addition of any type of surfactant used for electrospinning and the disorder becomes more pronounced when the anionic surfactant is utilized. Owing to the fact that microstructure defects create midband gap states that enable more electrons to be emitted from the fiber, an enhancement of electron emission is observed for PAN electrospun in the presence of the anionic surfactant. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 3726-3735, 2013 [ABSTRACT FROM AUTHOR]

We present here a facile method to produce macroporous-activated carbon nanofibers (AMP-CNFs) by post-treating electrospun cobalt(II) chloride (CoCl) containing polyacrylonitrile (PAN/CoCl) nanofibers with hydrogen sulfide (HS) followed by carbonization. A range of techniques including scanning and transmission electron microscopy, FTIR and Raman spectroscopy is used to examine and characterize the process. Because of the phase behavior between carbon and cobalt, cobalt particles are formed in the nanofibers, some of which leave the fibers during the heat treatment process leading to macroporous fibrous structures. The number of the macroporous increase significantly with increasing CoCl concentration in the precursor HS-treated PAN/CoCl nanofibers. The cobalt phase in the fibers also leads to catalytic graphitization of the carbon nanofibers. The produced AMP-CNFs may be a promising candidates in many applications including anode layer in lithium ion batteries, air and liquid purifiers in filters, as well as in biomedical applications. [ABSTRACT FROM AUTHOR]

Multifunctional Aerogels: Cellulose Silica Hybrid Nanofiber Aerogels: From Sol-Gel Electrospun Nanofibers to Multifunctional Aerogels (Adv. Funct. Keywords: 3D nanofibers; flame retardant; nanofiber aerogels; oil-water separation; polymer-silica hybrid; resilient and flexible 3D nanofibers, flame retardant, nanofiber aerogels, oil-water separation, polymer-silica hybrid, resilient and flexible. [Extracted from the article]

Aerogels are considered ideal candidates for various applications, because of their low bulk density, highly porous nature, and functional performance. However, the time intensive nature of the complex fabrication process limits their potential application in various fields. Recently, incorporation of a fibrous network has resulted in production of aerogels with improved properties and functionalities. A facile approach is presented to fabricate hybrid sol–gel electrospun silica‐cellulose diacetate (CDA)‐based nanofibers to generate thermally and mechanically stable nanofiber aerogels. Thermal treatment results in gluing the silica‐CDA network strongly together thereby enhancing aerogel mechanical stability and hydrophobicity without compromising their highly porous nature (>98%) and low bulk density (≈10 mg cm−3). X‐ray photoelectron spectroscopy and in situ Fourier‐transform infrared studies demonstrate the development of strong bonds between silica and the CDA network, which result in the fabrication of cross‐linked structure responsible for their mechanical and thermal robustness and enhanced affinity for oils. Superhydrophobic nature and high oleophilicity of the hybrid aerogels enable them to be ideal candidates for oil spill cleaning, while their flame retardancy and low thermal conductivity can be explored in various applications requiring stability at high temperatures. [ABSTRACT FROM AUTHOR]

Abstract: We report on the preparation and characterization of Ag/LiCoO2 nanofibers (NFs) via the sol–gel electrospinning (ES) technique. Ag nanoparticles (NPs) were produced in an aqueous polyvinyl pyrrolidone (PVP) solution by using AgNO3 precursor. A viscous lithium acetate/cobalt acetate/polyvinylalcohol/water (LiAc/(CoAc)2/PVA/water) solution was prepared separately. A Ag NPs/PVP/water solution was prepared and added to this viscous solution and magnetically stirred to obtain the final homogeneous electrospinning solution. After establishing the proper electrospinning conditions, as-spun precursor Ag/LiAc/Co(Ac)2/PVA/PVP NFs were formed and calcined in air at a temperature of 600°C for 3 h to form well-crystallized porous Ag/LiCoO2 NFs. Various analytical characterization techniques such as UV–vis, SEM, TEM, TGA, XRD, and XPS were performed to analyze Ag NPs, as-spun and calcined NFs. It was established that Ag NPs in the precursor Ag/LiAc/Co(Ac)2/PVA/PVP NFs are highly self-aligned as a result of the behavior of Ag in the electric field of the electrospinning setup and the interaction of Ag ions with Li and Co ions in the NF. Ag/LiCoO2 NFs exhibit a nanoporous structure compared with un-doped LiCoO2 NFs because the atomic radius of Ag is larger than the radius of Co and Li ion; thus, no substitution between Ag and Li or Ag and Co atoms occurs, and Ag NPs are located at the interlayer of LiCoO2 while some are left in the fiber. [Copyright &y& Elsevier]

Climate changes, emerging species of plant pests, and deficits of clean water and arable land have made availability of food to the ever-increasing global population a challenge. Excessive use of synthetic pesticides to meet ever-increasing production needs has resulted in development of resistance in pest populations, as well as significant ecotoxicity, which has directly and indirectly impacted all life-forms on earth. To meet the goal of providing safe, sufficient, and high-quality food globally with minimal environmental impact, one strategy is to focus on targeted delivery of pesticides using eco-friendly and biodegradable carriers that are derived from naturally available materials. Herein, we discuss some of the recent approaches to use biodegradable matrices in crop protection, while exploring their design and efficiency. We summarize by discussing associated challenges with the existing approaches and future trends that can lead the world to more sustainable agricultural practices. Image 1 • Providing food safety and security is critical for the growing global population. • Crop yield is affected by various biotic and abiotic factors. • Targeted/sustained delivery of agrochemicals reduces excessive use of pesticides. • Nature-derived biodegradable materials curtail plant health and environmental harm. • Biodegradable matrices hold promise for sustainable crop protection. [ABSTRACT FROM AUTHOR]

We report a single-step method to immobilize hyperthermophilic enzymes within chemically crosslinked polyvinyl alcohol (PVA) nanofibrous membranes. The polymer crosslinking that entraps the enzyme within the fiber is not affected by the particular enzyme and can thus be applied to any enzyme. Using a reactive electrospinning process, the chemical crosslinking that occurs during processing effectively entraps the enzyme within the fiber preventing enzyme leaching at elevated temperature establishing that the system is sufficiently robust for immobilization of hyperthermophilic enzymes. Upon immobilization, the enzyme retains 20% of its catalytic activity as well as its hyperthermophilicity, as the maximum activity occurs at ~90 °C, and that activity at 90 °C is an order of magnitude higher than at 37 °C. Furthermore, thermostability of the enzyme is enhanced upon immobilization as indicated by the 2-fold increase in half-life at 90 °C and pH 5.5 which extends the use of these biocatalysts at high temperatures. Compared to alternative methods, the apparent activity using the single-step method is significantly higher than alternative two-step methods (4 orders of magnitude higher than non-solvent based crosslinking and 3-fold higher than vapor-phase crosslinking). Analysis of this immobilization method indicates that the apparent decrease in specific activity could be attributed to enzyme deactivation arising from the crosslinking reaction, whereas mass transfer limits the apparent activity using alternative two-step immobilization methods. Based on this understanding, enzyme activity upon immobilization may be improved by using enzymes with higher intrinsic stability. Since significant enzyme activity is observed upon immobilization and the stability under high temperatures is enhanced, this versatile approach leverages the unique properties of hyperthermophilc enzymes and electrospun nanofibers providing a platform to produce catalytically active nanofibrous membranes appropriate for high temperature processes. [ABSTRACT FROM AUTHOR]

The ability to develop nanofibers containing whey proteins presents a unique opportunity to exploit the inherent benefits of whey protein with that of the desirable attributes of nanofibers. In this study, aqueous whey protein solutions, both whey protein isolate (WPI) and one of its major components beta-lactoglobulin (BLG), are electrospun into nanofibers in conjunction with a spinnable polymer, poly(ethylene oxide) (PEO). WP:PEO solution composition as high as 3:1 and with average fiber diameters ranging from 312 to 690 nm are produced depending on polymer composition and concentration. WP/PEO solutions are also successfully electrospun at acidic pH (2 ≤ pH ≤ 3), which could improve shelf life. FTIR analysis of WP/PEO fiber mat indicates some variation in WP secondary structure with varying WPI concentration (as WPI increases, % α-helix increases and β-turn decreases) and pH (as pH decreases from neutral (7.5) to acidic (2), % β-sheet decreases and α-helix increases). XPS also confirms the presence of WP on the surface of the blend fibers, augmenting the FTIR analysis. Interestingly, WP/PEO composite nanofibers maintain its fibrous morphology at temperatures as high as 100 °C, above the 60 °C PEO melting point. In addition, the mats swell in water and retain a fibrous quality which makes them desirable for application in regenerative medicine. Finally, we incorporate a small hydrophobic molecule Rhodamine B (RhB) as a model flavonoid into WP/PEO nanofiber mats. The BLG:PEO nanofibers qualitatively exhibit improved fiber quality and RhB distribution compared to PEO nanofibers; however, no effect on the release profile is observed. [ABSTRACT FROM AUTHOR]

Wepresent here a systematic investigation to understand why aqueoussodium alginate can only be electrospun into fibers through a blendwith another polymer; specifically, polyethylene oxide (PEO). We seekto examine and understand the role of PEO as the “carrier polymer”.The addition of PEO favorably reduces electrical conductivity andsurface tension of the alginate solution, aiding in fiber formation.While PEO has the ability to coordinate through its ether group (−COC−)with metal cation like the sodium cation of sodium alginate, we demonstratein this study using PEO as well as polyvinyl alcohol (PVA) that coordinationmay have little effect on electrospinnability. More importantly, weshow that PEO as carrier polymer provides molecular entanglement thatis required for electrospinning. Since the selected carrier polymerprovides the necessary entanglement, this carrier polymer must beelectrospinnable, entangled and of a high molecular weight (more than600 kDa for PEO). On the basis of these requirements, we stipulatethat the PEO–PEO interaction of the high molecular-weight entangledPEO is key to “carrying” the alginate from solutionto fibers during electrospinning. Further, using the resulting understandingof the role of PEO, we were able to increase the alginate concentrationby employing a higher molecular-weight PEO: up to 70 wt % alginateusing 2000 kDa PEO and, with, the addition of Triton X-100 surfactant,up to 85 wt % alginate, higher than previously reported. [ABSTRACT FROM AUTHOR]

Abstract: Meltblowing is a unique one-step process for producing self-bonded fibrous nonwoven membranes directly from polymer resins, with average fiber diameter ranging between 1 and 2μm. Determining routes for making nano- or submicron-fibers using this process are desirable since there are many manufacturing assets that are already in place. It is envisaged that these nonwoven membranes will find applications in critical areas such as medical, hygiene, filtration, bioseparation, and others. In this study, we investigate the influence of different die configurations and operating conditions on fiber and web characteristics. We also report on strategies for reducing the fiber size below one micron to achieve higher filtration quality at lower basis weight relative to the conventional meltblown webs. Their performance is compared to a control meltblown sample produced by using a typical die design. We find that production of nano-meltblown membranes with an average fiber size in the range of 300–500nm using this new die design is possible and report on process operating conditions that result in such structures. These samples achieve equal filtration efficiencies to that of our control sample at 88% reduced basis weight but at a lower polymer throughput. The lower basis weight also resulted in a lower pressure drop and overall, the new samples exhibited a higher quality factor, twice that of the control. These results show significant promise for the use of nano-meltblown fibers in filtration applications. [Copyright &y& Elsevier]

Abstract: We report here preparation of nanofibers containing alginate using two different molecular weights (MWs): 37kDa and 196kDa. Low MW alginates are attractive for in vivo tissue scaffolds where degradation and clearance from the body are desirable, whereas higher MW alginates are amenable for topical use as wound coverage because of its better mechanical properties. We use polyethylene oxide (PEO) as a carrier material to aid in electrospinning, and relate the solution properties, including entanglement concentration, relaxation time, conductivity, and surface tension, to their ability to be electrospun. In addition, we examine an FDA-approved, nonionic surfactant as a route to enhancing the alginate–PEO ratio (>80:20), and less toxic alternative to Triton X-100 surfactant. Finally, alginate-only nanofibers that are also water-insoluble are obtained by crosslinking the electrospun fibers with calcium and subsequently removing the PEO and surfactants by soaking the nanofibers in water. [Copyright &y& Elsevier]