Preparation of MnO nanofibers by novel hydrothermal treatment of manganese acetate/PVA electrospun nanofiber mats

Energy Technology Data Exchange (ETDEWEB)

Barakat, Nasser A.M. [Chemical Engineering Department, Faculty of Engineering, El-Minia University, El-Minia (Egypt); Center for Healthcare Technology Development, Chonbuk National University, Jeonju 561-756 (Korea, Republic of)], E-mail: nasbarakat@yahoo.com; Park, Soo Jin [Center for Healthcare Technology Development, Chonbuk National University, Jeonju 561-756 (Korea, Republic of); Khil, Myung Seob [Department of Textile Engineering, Chonbuk National University, Jeonju 561-756 (Korea, Republic of); Kim, Hak Yong [Center for Healthcare Technology Development, Chonbuk National University, Jeonju 561-756 (Korea, Republic of); Department of Textile Engineering, Chonbuk National University, Jeonju 561-756 (Korea, Republic of)], E-mail: khy@chonbuk.ac.kr

2009-06-15

In the present study, manganese monoxide (MnO) which is hard to prepare because of the chemical activity of the manganese metal has been synthesized in nanofibrous form. An electrospun manganese acetate/poly(vinyl alcohol) nanofiber mats have been hydrothermally treated by novel strategy. The treatment process was based on producing of water gas (Co and H{sub 2}) to eliminate the polymer and reduced the manganese acetate to manganese monoxide. The process was carried out by heating the dried nanofiber mates at 400 deg. C for 3 h in an especial designed reactor in which a stream of water vapor was passing through a bed of an activated carbon. The obtained physiochemical characterization results indicated that the proposed hydrothermal treatment process does have the ability to produce pure MnO nanofibers with good crystallinity.

A facile method for electrospinning of Ag nanoparticles/poly (vinyl alcohol)/carboxymethyl-chitosan nanofibers

International Nuclear Information System (INIS)

Zhao, Yinghui; Zhou, Ying; Wu, Xiaomian; Wang, Lu; Xu, Ling; Wei, Shicheng

2012-01-01

Highlights: ► AgNPs/PVA/CM-chitosan nanofibers were prepared via electrospinning method. ► AgNPs were in situ synthesized in electrospinning solution via a facile method. ► AgNPs distributed homogeneously on the surface of nanofibers. ► The prepared nanofibers possessed certain antibacterial ability against Escherichia coli. ► The AgNPs containing nanofibers had potential as antibacterial biomaterial. - Abstract: A facile method to prepare silver nanoparticles (AgNPs) containing nanofibers via electrospinning has been demonstrated. AgNPs were in situ synthesized in poly (vinyl alcohol) (PVA)/carboxymethyl-chitosan (CM-chitosan) blend aqueous solution before electrospinning. UV–vis spectra, viscosity and conductivity of the electrospinning solution were measured to investigate their effects on the electrospinning procedure. The morphology of AgNPs/PVA/CM-chitosan nanofibers was observed by Field Emission Scanning Electron Microscopy. The formation and morphology of AgNPs were investigated by Transmission Electron Microscopy and X-ray Photoelectron Spectroscopy. The resulted nanofibers have smooth surface and uniform diameters ranging from 295 to 343 nm. The diameters of AgNPs mainly distributed in the range of 4–14 nm, and the electrostatic interaction between AgNPs and fibers was observed. Finally, in vitro Ag release from the nanofibers was measured and the antibacterial behavior of the nanofibers against Escherichia coli was studied by bacterial growth inhibition halos and bactericidal kinetic testing. The AgNPs/PVA/CM-chitosan nanofibers possessed certain antibacterial ability, which makes them capable for antibacterial biomaterials.

Evaluation of proanthocyanidin-crosslinked electrospun gelatin nanofibers for drug delivering system

International Nuclear Information System (INIS)

Huang, Chiung-Hua; Chi, Chin-Ying; Chen, Yueh-Sheng; Chen, Kuo-Yu; Chen, Pei-Lain; Yao, Chun-Hsu

2012-01-01

Electrospun nanofibers are excellent candidates for various biomedical applications. We successfully fabricated proanthocyanidin‐crosslinked gelatin electrospun nanofibers. Proanthocyanidin, a low cytotoxic collagen crosslinking reagent, increased the gelatin crosslinking percentage in the nanofibers from 53% to 64%. The addition of proanthocyanidin kept the nanofibers from swelling, and, thus, made the fibers more stable in the aqueous state. The compatibility and the release behavior of the drug in the nanofibers were examined using magnesium ascorbyl phosphate as the model drug. Proanthocyanidin also promoted drug loading and kept the drug release rate constant. These properties make the proanthocyanidin‐crosslinked gelatin nanofibers an excellent material for drug delivery. In the cell culture study, L929 fibroblast cells had a significantly higher proliferation rate when cultured with the gelatin/proanthocyanidin blended nanofibers. This characteristic showed that proanthocyanidin‐crosslinked gelatin electrospun nanofibers could potentially be employed as a wound healing material by increasing cell spreading and proliferation. - Highlights: ► Proanthocyanidin‐crosslinked gelatin nanofibers (GEL/PA) is synthesized. ► Proanthocyanidin promoted drug loading and kept the drug release rate constant. ► The GEL/PA nanofibers accelerate fibroblast cell proliferation. ► The GEL/PA nanofibers increase the drug loading efficiency.

Fabrication of Conductive Polypyrrole Nanofibers by Electrospinning

Directory of Open Access Journals (Sweden)

Yiqun Cong

2013-01-01

Full Text Available Electrospinning is employed to prepare conductive polypyrrole nanofibers with uniform morphology and good mechanical strength. Soluble PPy was synthesized with NaDEHS as dopant and then applied to electrospinning with or without PEO as carrier. The PEO contents had great influence on the morphology and conductivity of the electrospun material. The results of these experiments will allow us to have a better understanding of PPy electrospun nanofibers and will permit the design of effective electrodes in the BMIs fields.

A Pendulum-Like Motion of Nanofiber Gel Actuator Synchronized with External Periodic pH Oscillation

Directory of Open Access Journals (Sweden)

Shuji Hasimoto

2011-02-01

Full Text Available In this study, we succeeded in manufacturing a novel nanofiber hydrogel actuator that caused a bending and stretching motion synchronized with external pH oscillation, based on a bromate/sulfite/ferrocyanide reaction. The novel nanofiber gel actuator was composed of electrospun nanofibers synthesized by copolymerizing acrylic acid and hydrophobic butyl methacrylate as a solubility control site. By changing the electrospinning flow rate, the nanofiber gel actuator introduced an anisotropic internal structure into the gel. Therefore, the unsymmetrical motion of the nanofiber actuator was generated.

Template synthesis and magnetic properties of highly aligned barium hexaferrite (BaFe12O19) nanofibers

International Nuclear Information System (INIS)

Huang, Boneng; Li, Congju; Wang, Jiaona

2013-01-01

Using electrospun poly(ethylene terephthalate)/citric acid (PET/CA) microfibers as the template, highly aligned barium hexaferrite (BaFe 12 O 19 ) nanofibers with diameters of ca. 800 nm and lengths up to 2 cm were synthesized by sol–gel precursor coating technique and subsequent high temperature calcination. Structural and morphological investigations revealed that individual BaFe 12 O 19 nanofibers were composed of numerous nanocrystallites stacking alternatively along the nanofiber axis, the average grain size was ca. 225 nm and the single crystallites on each BaFe 12 O 19 nanofibers were of random orientations. The formation mechanism of aligned BaFe 12 O 19 nanofibers was proposed based on experiment. The magnetic measurement revealed that the aligned BaFe 12 O 19 nanofibers exhibited orientation-dependent magnetic behavior with respect to the applied magnetic field. The magnetic anisotropy with the easy magnetizing axis along the length of the nanofibers was due to the shape anisotropy. Such aligned magnetic nanofibers can find relevance in application requiring an orientation-dependent physical response. - Highlights: ► A simple method was used to synthesize the aligned BaFe 12 O 19 nanofibers. ► The aligned BaFe 12 O 19 nanofibers display an obvious orientation-dependent magnetic behavior. ► The method can be readily applied to other aligned one-dimensional inorganic nanomaterials

A facile method for electrospinning of Ag nanoparticles/poly (vinyl alcohol)/carboxymethyl-chitosan nanofibers

Energy Technology Data Exchange (ETDEWEB)

Zhao, Yinghui; Zhou, Ying [Beijing Key Laboratory for Solid Waste Utilization and Management, College of Engineering, Peking University, Beijing 100871 (China); Center for Biomedical Materials and Tissue Engineering, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871 (China); Wu, Xiaomian [Center for Biomedical Materials and Tissue Engineering, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871 (China); Department of Orthodontics College of Stomatology, Chongqing Medical University, Chongqing 401147 (China); Wang, Lu [Beijing Key Laboratory for Solid Waste Utilization and Management, College of Engineering, Peking University, Beijing 100871 (China); Xu, Ling, E-mail: lingxu@pku.edu.cn [Beijing Key Laboratory for Solid Waste Utilization and Management, College of Engineering, Peking University, Beijing 100871 (China); Center for Biomedical Materials and Tissue Engineering, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871 (China); PKU-HKUST ShenZhen-HongKong Institution, Shenzhen 518057 (China); Wei, Shicheng, E-mail: sc-wei@pku.edu.cn [Center for Biomedical Materials and Tissue Engineering, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871 (China); Department of Oral and Maxillofacial Surgery, School and Hospital of Stomatology, Peking University, Beijing 100081 (China)

2012-09-01

Highlights: Black-Right-Pointing-Pointer AgNPs/PVA/CM-chitosan nanofibers were prepared via electrospinning method. Black-Right-Pointing-Pointer AgNPs were in situ synthesized in electrospinning solution via a facile method. Black-Right-Pointing-Pointer AgNPs distributed homogeneously on the surface of nanofibers. Black-Right-Pointing-Pointer The prepared nanofibers possessed certain antibacterial ability against Escherichia coli. Black-Right-Pointing-Pointer The AgNPs containing nanofibers had potential as antibacterial biomaterial. - Abstract: A facile method to prepare silver nanoparticles (AgNPs) containing nanofibers via electrospinning has been demonstrated. AgNPs were in situ synthesized in poly (vinyl alcohol) (PVA)/carboxymethyl-chitosan (CM-chitosan) blend aqueous solution before electrospinning. UV-vis spectra, viscosity and conductivity of the electrospinning solution were measured to investigate their effects on the electrospinning procedure. The morphology of AgNPs/PVA/CM-chitosan nanofibers was observed by Field Emission Scanning Electron Microscopy. The formation and morphology of AgNPs were investigated by Transmission Electron Microscopy and X-ray Photoelectron Spectroscopy. The resulted nanofibers have smooth surface and uniform diameters ranging from 295 to 343 nm. The diameters of AgNPs mainly distributed in the range of 4-14 nm, and the electrostatic interaction between AgNPs and fibers was observed. Finally, in vitro Ag release from the nanofibers was measured and the antibacterial behavior of the nanofibers against Escherichia coli was studied by bacterial growth inhibition halos and bactericidal kinetic testing. The AgNPs/PVA/CM-chitosan nanofibers possessed certain antibacterial ability, which makes them capable for antibacterial biomaterials.

Synergistic tungsten oxide/organic framework hybrid nanofibers for electrochromic device application

Science.gov (United States)

Dulgerbaki, Cigdem; Komur, Ali Ihsan; Nohut Maslakci, Neslihan; Kuralay, Filiz; Uygun Oksuz, Aysegul

2017-08-01

We report the first successful applications of tungsten oxide/conducting polymer hybrid nanofiber assemblies in electrochromic devices. Poly(3,4-ethylenedioxythiophene)/tungsten oxide (PEDOT/WO3) and polypyrrole/tungsten oxide (PPy/WO3) composites were prepared by an in situ chemical oxidative polymerization of monomers in different ionic liquids; 1-butyl-3-methylimidazolium tetrafluoroborate (BMIMBF4), 1-butyl-3-methylimidazolium hexafluorophosphate (BMIMPF6), 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl) imide (BMIMTFSI) and 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl) imide (BMPTFSI). Electrospinning process was used to form hybrid nanofibers from chemically synthesized nanostructures. The electrospun hybrid samples were compared from both morphological and electrochemical perspectives. Importantly, deposition of nanofibers from chemically synthesized hybrids can be achieved homogenously, on nanoscale dimensions. The morphologies of these assemblies were evaluated by SEM, whereas their electroactivity was characterized by cyclic voltammetry. Electrochromic devices made from hybrid nanofiber electrodes exhibited highest chromatic contrast of 37.66% for PEDOT/WO3/BMIMPF6, 40.42% for PPy/WO3/BMIMBF4 and show a strong electrochromic color change from transparent to light brown. Furthermore, the nanofiber devices exhibit outstanding stability when color switching proceeds, which may ensure a versatile platform for color displays, rear-view mirrors and smart windows.

Branched carbon nanofiber network synthesis at room temperature using radio frequency supported microwave plasmas

International Nuclear Information System (INIS)

Boskovic, Bojan O.; Stolojan, Vlad; Zeze, Dagou A.; Forrest, Roy D.; Silva, S. Ravi P.; Haq, Sajad

2004-01-01

Carbon nanofibers have been grown at room temperature using a combination of radio frequency and microwave assisted plasma-enhanced chemical vapor deposition. The nanofibers were grown, using Ni powder catalyst, onto substrates kept at room temperature by using a purposely designed water-cooled sample holder. Branched carbon nanofiber growth was obtained without using a template resulting in interconnected carbon nanofiber network formation on substrates held at room temperature. This method would allow room-temperature direct synthesized nanofiber networks over relatively large areas, for a range of temperature sensitive substrates, such as organic materials, plastics, and other polymers of interest for nanoelectronic two-dimensional networks, nanoelectromechanical devices, nanoactuators, and composite materials

Preparation of graphene oxide/poly (3,4-ethylenedioxytriophene): Poly (styrene sulfonate) (PEDOT:PSS) electrospun nanofibers

International Nuclear Information System (INIS)

Efelina, Vita; Widianto, Eri; Rusdiana, Dadi; Nugroho, A. A.; Kusumaatmaja, Ahmad; Triyana, Kuwat; Santoso, Iman

2016-01-01

Graphene oxide (GO)/Poly (3,4-Ethylenedioxytriophene):Poly (styrene Sulfonate) (PEDOT:PSS) nanofibers have been successfully fabricated by a simple electrospinning technique to develop conductive nanofibers with polyvinyl alcohol (PVA) act as a carrier solution. Graphene oxide has been synthesized by Hummer’s method and has been confirmed by Raman Spectroscopy, FTIR and UV-Vis Spectroscopy. GO/PEDOT:PSS composite nanofibers. The structural and morphological properties were characterized by Scanning Electron Microscopy (SEM). The result of SEM show that GO/PEDOT:PSS nanofibers has a relatively uniform morphology nanofiber with diameter between 180 nm - 340 nm with smooth nanofiber surface. The produced nanofibers from this study can be utilized for various applications such as flexible, conductive and transparent electrode.

Preparation of graphene oxide/poly (3,4-ethylenedioxytriophene): Poly (styrene sulfonate) (PEDOT:PSS) electrospun nanofibers

Energy Technology Data Exchange (ETDEWEB)

Efelina, Vita; Widianto, Eri [Department of Physics, Universitas Gadjah Mada, Sekip Utara BLS.21 Yogyakarta, 55281 Indonesia (Indonesia); Rusdiana, Dadi [Department of Physical Education, Universitas Pendidikan Indonesia, Bandung (Indonesia); Nugroho, A. A. [Department of Physics, Institut Teknologi Bandung, Jl. Ganesha 10 Bandung (Indonesia); Kusumaatmaja, Ahmad; Triyana, Kuwat; Santoso, Iman, E-mail: iman.santoso@ugm.ac.id [Department of Physics, Universitas Gadjah Mada, Sekip Utara BLS.21 Yogyakarta, 55281 Indonesia (Indonesia); Nanomaterials Research Group, Universitas Gadjah Mada,, Sekip Utara, Yogyakarta (Indonesia)

2016-04-19

Graphene oxide (GO)/Poly (3,4-Ethylenedioxytriophene):Poly (styrene Sulfonate) (PEDOT:PSS) nanofibers have been successfully fabricated by a simple electrospinning technique to develop conductive nanofibers with polyvinyl alcohol (PVA) act as a carrier solution. Graphene oxide has been synthesized by Hummer’s method and has been confirmed by Raman Spectroscopy, FTIR and UV-Vis Spectroscopy. GO/PEDOT:PSS composite nanofibers. The structural and morphological properties were characterized by Scanning Electron Microscopy (SEM). The result of SEM show that GO/PEDOT:PSS nanofibers has a relatively uniform morphology nanofiber with diameter between 180 nm - 340 nm with smooth nanofiber surface. The produced nanofibers from this study can be utilized for various applications such as flexible, conductive and transparent electrode.

Fabrication of indium sulfide nanofibers via a hydrothermal method assisted by AAO template

International Nuclear Information System (INIS)

Zhu Xiaoyi; Ma Junfeng; Wang Yonggang; Tao Jiantao; Zhou Jun; Zhao Zhongqiang; Xie Lijin; Tian Hua

2006-01-01

β-In 2 S 3 nanofibers were successfully synthesized via a hydrothermal method with AAO membrane as a template at 150 deg. C for 15 h. XRD patterns indicated the perfect crystallization of β-In 2 S 3 . SEM images showed that the β-In 2 S 3 nanofibers grew up from the channel ends of the AAO template. TEM images confirmed that the nanofibers had a high aspect ratio of ca. 40-50 and diameters of about 10 nm. The room temperature photoluminescence (PL) spectrum of the β-In 2 S 3 nanofibers indicated its potential applications in light-emission devices

Synthesis of titanate, TiO2 (B), and anatase TiO2 nanofibers from natural rutile sand

International Nuclear Information System (INIS)

Pavasupree, Sorapong; Suzuki, Yoshikazu; Yoshikawa, Susumu; Kawahata, Ryoji

2005-01-01

Titanate nanofibers were synthesized by hydrothermal method (150 deg. C for 72 h) using natural rutile sand as the starting materials. TiO 2 (B) and anatase TiO 2 (high crystallinity) nanofibers with the diameters of 20-100 nm and the lengths of 10-100 μm were obtained by calcined titanate nanofibers for 4 h at 400 and 700 deg. C (in air), respectively. The samples characterized by XRD, SEM, TEM, SAED, HRTEM, and BET surface area. This synthesis method provides a simple route to fabricate one-dimensional nanostructured TiO 2 from low cost material. -- Graphical abstract: Titanate nanofibers (b) were synthesized by hydrothermal method (150 deg. C for 72 h) using natural rutile sand (a) as the starting materials. TiO 2 (B) (c) and anatase TiO 2 (d) nanofibers with the diameters of 20-50 nm and the lengths of 10-100 μm were obtained by calcined titanate nanofibers for 4 h at 400 deg. C and 700 deg. C (in air), respectively

Carbon nanotubes and nanofibers synthesized by CVD on nickel coatings deposited with a vacuum arc

Energy Technology Data Exchange (ETDEWEB)

Escobar, M. [LP and MC, Dep. de Fisica-FCEyN-UBA, Cdad. Universitaria Pab.1, (1428), Buenos Aires (Argentina); DQIAQF-FCEyN-UBA, Cdad. Universitaria Pab.1, (1428), Buenos Aires (Argentina); Giuliani, L. [INFIP, CONICET, Dep. de Fisica, FCEyN-UBA, Cdad. Univ. Pab.1, (1428), Buenos Aires (Argentina); Candal, R.J. [INQUIMAE-FCEyN-UBA, Cdad. Universitaria Pab.2, (1428), Buenos Aires (Argentina); Lamas, D.G. [CINSO, CITEFA, CONICET, J.B. de La Salle 4397, (1603) V.Martelli, Buenos Aires (Argentina); Caso, A. [LP and MC, Dep. de Fisica-FCEyN-UBA, Cdad. Universitaria Pab.1, (1428), Buenos Aires (Argentina); Rubiolo, G. [LP and MC, Dep. de Fisica-FCEyN-UBA, Cdad. Universitaria Pab.1, (1428), Buenos Aires (Argentina); UAM-CNEA, Av. Gral Paz 1499, (1650) San Martin, Buenos Aires (Argentina); Grondona, D. [INFIP, CONICET, Dep. de Fisica, FCEyN-UBA, Cdad. Univ. Pab.1, (1428), Buenos Aires (Argentina); Goyanes, S. [LP and MC, Dep. de Fisica-FCEyN-UBA, Cdad. Universitaria Pab.1, (1428), Buenos Aires (Argentina); Marquez, A., E-mail: amarquez@df.uba.a [INFIP, CONICET, Dep. de Fisica, FCEyN-UBA, Cdad. Univ. Pab.1, (1428), Buenos Aires (Argentina)

2010-04-16

Nanotubes and nanofibers were grown on Ni coatings deposited by plasma generated with a pulsed vacuum arc on silicon wafers using three different bias conditions: at floating potential (approximately +30 V respect to the grounded cathode); at ground potential; and at -60 V. An atomic force microscopy study showed that the Ni film morphology was affected by the bias condition of the substrate. The morphology of carbonaceous species depended on Ni-films characteristics. FE-SEM and TEM analyses have shown that nanofibers growth was favoured on Ni coatings deposited at -60 V whereas nanotubes grew mainly on Ni coatings obtained at floating and ground potentials. Hence, this new method to produce the precursor can be optimized to obtain nanotubes or nanofibers varying the substrate bias for the Ni deposition.

Improving effects of chitosan nanofiber scaffolds on osteoblast proliferation and maturation

Science.gov (United States)

Ho, Ming-Hua; Liao, Mei-Hsiu; Lin, Yi-Ling; Lai, Chien-Hao; Lin, Pei-I; Chen, Ruei-Ming

2014-01-01

Osteoblast maturation plays a key role in regulating osteogenesis. Electrospun nanofibrous products were reported to possess a high surface area and porosity. In this study, we developed chitosan nanofibers and examined the effects of nanofibrous scaffolds on osteoblast maturation and the possible mechanisms. Macro- and micro observations of the chitosan nanofibers revealed that these nanoproducts had a flat surface and well-distributed fibers with nanoscale diameters. Mouse osteoblasts were able to attach onto the chitosan nanofiber scaffolds, and the scaffolds degraded in a time-dependent manner. Analysis by scanning electron microscopy further showed mouse osteoblasts adhered onto the scaffolds along the nanofibers, and cell–cell communication was also detected. Mouse osteoblasts grew much better on chitosan nanofiber scaffolds than on chitosan films. In addition, human osteoblasts were able to adhere and grow on the chitosan nanofiber scaffolds. Interestingly, culturing human osteoblasts on chitosan nanofiber scaffolds time-dependently increased DNA replication and cell proliferation. In parallel, administration of human osteoblasts onto chitosan nanofibers significantly induced osteopontin, osteocalcin, and alkaline phosphatase (ALP) messenger (m)RNA expression. As to the mechanism, chitosan nanofibers triggered runt-related transcription factor 2 mRNA and protein syntheses. Consequently, results of ALP-, alizarin red-, and von Kossa-staining analyses showed that chitosan nanofibers improved osteoblast mineralization. Taken together, results of this study demonstrate that chitosan nanofibers can stimulate osteoblast proliferation and maturation via runt-related transcription factor 2-mediated regulation of osteoblast-associated osteopontin, osteocalcin, and ALP gene expression. PMID:25246786

Synthesis and Property of Ag(NP)/catechin/Gelatin Nanofiber

Science.gov (United States)

Nasir, Muhamad; Apriani, Dita

2017-12-01

Nanomaterial play important role future industry such as for the medical, food, pharmaceutical and cosmetic industry. Ag (NP) and catechin exhibit antibacterial property. Ag(NP) with diameter around 15 nm was synthesis by microwaved method. We have successfully produce Ag(NP)/catechin/gelatin nanofiber composite by electrospinning process. Ag(NP)/catechin/gelatin nanofiber was synthesized by using gelatin from tuna fish, polyethylene oxide (PEO), acetic acid as solvent and silver nanoparticle(NP)/catechin as bioactive component, respectively. Morphology and structure of bioactive catechin-gelatin nanofiber were characterized by scanning electron microscopy (SEM) and fourier transform infrared spectroscopy (FTIR), respectively. SEM analysis showed that morphology of nanofiber composite was smooth and had average diameter 398.97 nm. FTIR analysis results were used to confirm structure of catechin-gelatin nanofiber. It was confirmed by FTIR that specific vibration band peak amide A (N-H) at 3286,209 cm-1, amide B (N-H) 3069,396 cm-1, amide I (C=O) at 1643,813 cm-1, amide II (N-H and CN) at 1538,949 cm-1, amide III (C-N) at 1276,789 cm-1, C-O-C from polyethylene oxide at 1146,418 cm-1, respectively. When examined to S. Aureus bacteria, Ag/catechin/gelatin nanofiber show inhabitation performance around 40.44%. Ag(NP)/catechin/gelatin nanofiber has potential application antibacterial medical application.

PANI-nanofibers/polyethylene blends: preparation and properties; Blendas de nanofibras de PANI/polietileno: preparacao e propriedades

Energy Technology Data Exchange (ETDEWEB)

Oliveira, F.; Hubler, R.; Basso, N.R.S., E-mail: nrbass@pucrs.b [Pontificia Universidade Catolica do Rio Grande do Sul (PUC-RS), Porto Alegre, RS (Brazil); Fim, F.C.; Galland, G.B. [Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, RS (Brazil)

2010-07-01

In this work polyaniline nanofibers (PANI-nanofibers) were prepared via interfacial polymerization. The PANI-nanofibers were dispersed in polyethylene (PE) matrix by in situ polymerization of ethylene using Cp{sub 2}ZrCl{sub 2} [bis(cyclopentadienyl) zirconium(IV) dichloride)] and methylaluminoxane as catalytic system. The composites were characterized by infra-red spectroscopy, X-ray diffraction, thermal analysis, transmission electron microscopy and scanning electron microscopy. The results show that nanofibers with average diameters of 200 nm were synthesized and that it was obtained well dispersed PE/PANI nanocomposites. The PANI-nanofibers load did not affect the catalytic activity, but it decreased crystallinity degree of nanocomposites. (author)

Antioxidant activity and haemolysis prevention efficiency of polyaniline nanofibers

Energy Technology Data Exchange (ETDEWEB)

Banerjee, Somik; Kumar, A [Materials Research Laboratory, Department of Physics, Tezpur University, Tezpur 784028, Assam (India); Saikia, Jyoti P; Konwar, B K, E-mail: ask@tezu.ernet.in [Department of Molecular Biology and Biotechnology, Tezpur University, Tezpur 784028, Assam (India)

2010-01-29

Polyaniline (PAni) nanofibers have been synthesized by interfacial polymerization using hydrochloric acid (HCl) and camphor sulfonic acid (CSA) as dopants. The powder x-ray diffraction pattern of bulk polyaniline reveals ES I structure and has been indexed in a pseudo-orthorhombic lattice. The broadening of (110) reflection in the nanofiber samples has been analysed in terms of domain length and strain using a convolution method employing a Voigt function. The increase in d spacing for the (110) reflection in HCl-doped PAni nanofibers have been assigned to the change in structural conformation due to the increase in the tilt angle of the polymer chain, which is also evident from microRaman spectra. UV-vis spectra of the PAni nanofibers exhibit a remarkable blueshift in the absorption bands attributed to {pi}-{pi}{sup *} and {pi}-polaron band transitions indicating a reduction in particle size, which is also observed in TEM micrographs. The antioxidant activity of the polyaniline nanofiber samples has been investigated using 1,1-diphenyl-2-picrylhydrazyl (DPPH) scavenging assay by employing UV-visible spectroscopy. It has also been observed that polyaniline nanofibers are able to protect the haemolysis of red blood cells (RBCs) from cytotoxic agents, namely H{sub 2}O{sub 2}. The observed enhancement in the antioxidant and haemolysis prevention activity of the PAni nanofibers as compared to bulk has been attributed to the reduction in particle size and changes in structural conformation, as evident from TEM, XRD and microRaman spectroscopy.

Surface plasmon resonances, optical properties, and electrical conductivity thermal hystersis of silver nanofibers produced by the electrospinning technique.

Science.gov (United States)

Barakat, Nasser A M; Woo, Kee-Do; Kanjwal, Muzafar A; Choi, Kyung Eun; Khil, Myung Seob; Kim, Hak Yong

2008-10-21

In the present study, silver metal nanofibers have been successfully prepared by using the electrospinning technique. Silver nanofibers have been produced by electrospinning a sol-gel consisting of poly(vinyl alcohol) and silver nitrate. The dried nanofiber mats have been calcined at 850 degrees C in an argon atmosphere. The produced nanofibers do have distinct plasmon resonance compared with the reported silver nanoparticles. Contrary to the introduced shapes of silver nanoparticles, the nanofibers have a blue-shifted plasmon resonance at 330 nm. Moreover, the optical properties study indicated that the synthesized nanofibers have two band gap energies of 0.75 and 2.34 eV. An investigation of the electrical conductivity behavior of the obtained nanofibers shows thermal hystersis. These privileged physical features greatly widen the applications of the prepared nanofibers in various fields.

Reactive electrospinning and biodegradation of cross-linked methacrylated polycarbonate nanofibers

Energy Technology Data Exchange (ETDEWEB)

Wu Ruizhi; Zhang Jianfeng; Fan Yuwei; Xu Xiaoming [Department of Comprehensive Dentistry and Biomaterials, Louisiana State University Health Sciences Center, 1100 Florida Avenue, Box 137, New Orleans, LA 70119 (United States); Stoute, Diana; Lallier, Thomas, E-mail: xxu@lsuhsc.edu [Department of Cell Biology and Anatomy, Louisiana State University Health Science Center, 1100 Florida Avenue, Box 137, New Orleans, LA 70119 (United States)

2011-06-15

The objectives of this study were to fabricate cross-linked biodegradable polycarbonate nanofibers and to investigate their biodegradability by different enzymes. Poly(2,3-dihydroxycarbonate) was synthesized from naturally occurring l-tartaric acid. The hydroxyl groups on the functional polycarbonate were converted to methacrylate groups to enable the polymer to cross-link under UV irradiation. Smooth cross-linked methacrylated polycarbonate nanofibers (300-1800 nm) were fabricated by a reactive electrospinning process with in situ UV radiation from a mixed solution of linear methacrylated polycarbonate (MPC) and poly(ethylene oxide) (PEO) (MPC:PEO = 9:1) in methanol/chloroform (50/50). These cross-linked nanofibers have shown excellent solvent resistance and their solubility decreases with increasing degree of cross-linking. The thermal properties of linear and cross-linked polycarbonate nanofibers were investigated by differential scanning calorimetry and thermogravimetric analysis. The cross-linked polycarbonate nanofibers show no melting point below 200 {sup 0}C and their decomposition temperature increases with increasing cross-linking degree. Their biodegradation products by five different enzymes were analyzed using liquid chromatography-mass spectrometry (LC-MS). The biodegradability of the polycarbonate nanofibers decreases with increasing cross-linking degree. These nanofibers were found to support human fibroblast survival and to promote cell attachment. This study demonstrates that cross-linked biodegradable polycarbonate nanofibers with different chemical properties and biodegradability can be fabricated using the novel reactive electrospinning technology to meet the needs of different biomedical applications.

Synthesis of aluminum oxy-hydroxide nanofibers from porous anodic alumina

Energy Technology Data Exchange (ETDEWEB)

Jha, Himendra; Kikuchi, Tatsuya; Sakairi, Masatoshi; Takahashi, Hideaki [Laboratory of Interface Microstructure Analysis (LIMSA), Division of Materials Science and Engineering, Graduate School of Engineering, Hokkaido University, Sapporo 060-8628 (Japan)], E-mail: himendra@eng.hokudai.ac.jp

2008-10-01

A novel method for the synthesis of aluminum oxy-hydroxide nanofibers from a porous anodic oxide film of aluminum is demonstrated. In the present method, the porous anodic alumina not only acts as a template, but also serves as the starting material for the synthesis. The porous anodic alumina film is hydrothermally treated for pore-sealing, which forms aluminum oxy-hydroxide inside the pores of the oxide film as well as on the surface of the film. The hydrothermally sealed porous oxide film is immersed in the sodium citrate solution, which selectively etches the porous aluminum oxide from the film, leaving the oxy-hydroxide intact. The method is simple and gives highly uniform aluminum oxy-hydroxide nanofibers. Moreover, the diameter of the nanofibers can be controlled by controlling the pore size of the porous anodic alumina film, which depends on the anodizing conditions. Nanofibers with diameters of about 38-85 nm, having uniform shape and size, were successfully synthesized using the present method.

Preparation of Pd/Bacterial Cellulose Hybrid Nanofibers for Dopamine Detection

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Dawei Li

2016-05-01

Full Text Available Palladium nanoparticle-bacterial cellulose (PdBC hybrid nanofibers were synthesized by in-situ chemical reduction method. The obtained PdBC nanofibers were characterized by a series of analytical techniques. The results revealed that Pd nanoparticles were evenly dispersed on the surfaces of BC nanofibers. Then, the as-prepared PdBC nanofibers were mixed with laccase (Lac and Nafion to obtain mixture suspension, which was further modified on electrode surface to construct novel biosensing platform. Finally, the prepared electrochemical biosensor was employed to detect dopamine. The analysis result was satisfactory, the sensor showed excellent electrocatalysis towards dopamine with high sensitivity (38.4 µA·mM−1, low detection limit (1.26 µM, and wide linear range (5–167 µM. Moreover, the biosensor also showed good repeatability, reproducibility, selectivity and stability and was successfully used in the detection of dopamine in human urine, thus providing a promising method for dopamine analysis in clinical application.

Synthesis of aluminum oxy-hydroxide nanofibers from porous anodic alumina

International Nuclear Information System (INIS)

Jha, Himendra; Kikuchi, Tatsuya; Sakairi, Masatoshi; Takahashi, Hideaki

2008-01-01

A novel method for the synthesis of aluminum oxy-hydroxide nanofibers from a porous anodic oxide film of aluminum is demonstrated. In the present method, the porous anodic alumina not only acts as a template, but also serves as the starting material for the synthesis. The porous anodic alumina film is hydrothermally treated for pore-sealing, which forms aluminum oxy-hydroxide inside the pores of the oxide film as well as on the surface of the film. The hydrothermally sealed porous oxide film is immersed in the sodium citrate solution, which selectively etches the porous aluminum oxide from the film, leaving the oxy-hydroxide intact. The method is simple and gives highly uniform aluminum oxy-hydroxide nanofibers. Moreover, the diameter of the nanofibers can be controlled by controlling the pore size of the porous anodic alumina film, which depends on the anodizing conditions. Nanofibers with diameters of about 38-85 nm, having uniform shape and size, were successfully synthesized using the present method

Controllable synthesis of helical, straight, hollow and nitrogen-doped carbon nanofibers and their magnetic properties

Energy Technology Data Exchange (ETDEWEB)

Li, Xun [State Key Laboratory of Coordination Chemistry, Nanjing National Laboratory of Microstructure, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093 (China); State Key Laboratory of Soil and Sustainable Agriculture, Institute of Soil Science, Chinese Academy of Sciences, Nanjing 210008 (China); Xu, Zheng, E-mail: zhengxu@nju.edu.cn [State Key Laboratory of Coordination Chemistry, Nanjing National Laboratory of Microstructure, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093 (China)

2012-12-15

Graphical abstract: The helical, straight and hollow carbon nanofibers can be selectively synthesized by adjusting either the reaction temperature or feed gas composition. Display Omitted Highlights: ► CNFs were synthesized via pyrolysis of acetylene on copper NPs. ► The helical, straight, hollow and N-doped CNFs can be selectively synthesized. ► The growth mechanism of different types of CNFs was proposed. -- Abstract: Carbon nanofibers (CNFs) with various morphologies were synthesized by catalytic pyrolysis of acetylene on copper nanoparticles which were generated from the in situ decomposition of copper acetylacetonate. The morphology of the pristine and acid-washed CNFs was investigated by field emission scanning electron microscope and high-resolution transmission electron microscope. Helical, straight and hollow CNFs can be selectively synthesized by adjusting either the reaction temperature or feed gas composition. The growth mechanism for these three types of CNFs was proposed.

Bioactive Glass Nanoparticles-Loaded Poly(ɛ-caprolactone Nanofiber as Substrate for ARPE-19 Cells

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Tadeu Henrique Lima

2016-01-01

Full Text Available Bioactive glass nanoparticles-loaded poly(ɛ-caprolactone nanofibers (BIOG PCL nanofibers were synthesized and evaluated as substrates for ocular cells (ARPE-19. BIOG PCL nanofibers were characterized using SEM, FTIR, and DSC, and the in vitro degradation profile was also investigated. The in vitro ocular biocompatibility of nanofibers was exploited in Müller glial cells (MIO-M1 cells and in chorioallantoic membrane (CAM; and the proliferative capacity, cytotoxicity, and functionality were evaluated. Finally, ARPE-19 cells were seeded onto BIOG PCL nanofibers and they were investigated as supports for in vitro cell adhesion and proliferation. SEM images revealed the incorporation of BIOG nanoparticles into PCL nanofibers. Nanoparticles did not induce modifications in the chemical structure and semicrystalline nature of PCL in the nanofiber, as shown by FTIR and DSC. MIO-M1 cells exposed to BIOG PCL nanofibers showed viability, and they were able to proliferate and to express GFAP, indicating cellular functionality. Moreover, nanofibers were well tolerated by CAM. These findings suggested the in vitro ocular biocompatibility and absence of toxicity of these nanofibers. Finally, the BIOG nanoparticles modulated the protein adsorption, and, subsequently, ARPE-19 cells adhered and proliferated onto the nanostructured supports, establishing cell-substrate interactions. In conclusion, the biodegradable and biocompatible BIOG PCL nanofibers supported the ARPE-19 cells.

Superhydrophobic terpolymer nanofibers containing perfluoroethyl alkyl methacrylate by electrospinning

Energy Technology Data Exchange (ETDEWEB)

Cengiz, Ugur, E-mail: ucengiz@gyte.edu.tr [Department of Chemical Engineering, Gebze Institute of Technology, Cayirova, 41400 Kocaeli (Turkey); Avci, Merih Z. [Polymer Science and Technology, Deparment of Chemistry, Istanbul Technical University, Maslak 34469, Istanbul (Turkey); Erbil, H. Yildirim [Department of Chemical Engineering, Gebze Institute of Technology, Cayirova, 41400 Kocaeli (Turkey); Sarac, A. Sezai [Polymer Science and Technology, Deparment of Chemistry, Istanbul Technical University, Maslak 34469, Istanbul (Turkey)

2012-05-15

A new statistical terpolymer containing perfluoroethyl alkyl methacrylate (Zonyl-TM), methyl methacrylate and butyl acrylate, poly(Zonyl-TM-ran-MMA-ran-BA) was synthesized in supercritical carbon dioxide at 200 bar and 80 Degree-Sign C using AIBN as an initiator by heterogeneous free radical copolymerization. Nanofibers of this terpolymer were produced by electrospinning from its DMF solution. The structural and thermal properties of terpolymers and electrospun poly(Zonyl-TM-MMA-BA) nanofibers were analyzed using Fourier transform infrared spectroscopy, nuclear magnetic resonance spectroscopy and differential scanning calorimetry. Nanofiber morphology was investigated by scanning electron microscopy. Electrospun nanofiber layer was found to be superhydrophobic with a water contact angle of 172 {+-} 1 Degree-Sign and highly oleophobic with hexadecane, glycerol and ethylene glycol contact angles of 70 {+-} 1 Degree-Sign , 167 {+-} 1 Degree-Sign and 163 {+-} 1 Degree-Sign respectively. The change of the contact angle results on the electrospun fiber layer and flat terpolymer surfaces by varying feed monomer composition were compared and discussed in the text.

Towards scalable binderless electrodes: carbon coated silicon nanofiber paper via Mg reduction of electrospun SiO2 nanofibers.

Science.gov (United States)

Favors, Zachary; Bay, Hamed Hosseini; Mutlu, Zafer; Ahmed, Kazi; Ionescu, Robert; Ye, Rachel; Ozkan, Mihrimah; Ozkan, Cengiz S

2015-02-06

The need for more energy dense and scalable Li-ion battery electrodes has become increasingly pressing with the ushering in of more powerful portable electronics and electric vehicles (EVs) requiring substantially longer range capabilities. Herein, we report on the first synthesis of nano-silicon paper electrodes synthesized via magnesiothermic reduction of electrospun SiO2 nanofiber paper produced by an in situ acid catalyzed polymerization of tetraethyl orthosilicate (TEOS) in-flight. Free-standing carbon-coated Si nanofiber binderless electrodes produce a capacity of 802 mAh g(-1) after 659 cycles with a Coulombic efficiency of 99.9%, which outperforms conventionally used slurry-prepared graphite anodes by over two times on an active material basis. Silicon nanofiber paper anodes offer a completely binder-free and Cu current collector-free approach to electrode fabrication with a silicon weight percent in excess of 80%. The absence of conductive powder additives, metallic current collectors, and polymer binders in addition to the high weight percent silicon all contribute to significantly increasing capacity at the cell level.

Influence of temperature on the photodegradation process using Ag-doped TiO2 nanostructures: Negative impact with the nanofibers

DEFF Research Database (Denmark)

Barakata, Nasser A.M.; Kanjwal, Muzafar Ahmed; Chronakis, Ioannis S.

2013-01-01

In this study, the influence of the temperature on the photodegradation process using Ag-doped TiO2 nanostructures was investigated. Two morphologies were used; nanoparticles and nanofibers. The nanofibers were synthesized by electrospinning of a sol–gel consisting of titanium isopropoxide, silve...

Fabrication of Aligned Polyaniline Nanofiber Array via a Facile Wet Chemical Process.

Science.gov (United States)

Sun, Qunhui; Bi, Wu; Fuller, Thomas F; Ding, Yong; Deng, Yulin

2009-06-17

In this work, we demonstrate for the first time a template free approach to synthesize aligned polyaniline nanofiber (PN) array on a passivated gold (Au) substrate via a facile wet chemical process. The Au surface was first modified using 4-aminothiophenol (4-ATP) to afford the surface functionality, followed subsequently by an oxidation polymerization of aniline (AN) monomer in an aqueous medium using ammonium persulfate as the oxidant and tartaric acid as the doping agent. The results show that a vertically aligned PANI nanofiber array with individual fiber diameters of ca. 100 nm, heights of ca. 600 nm and a packing density of ca. 40 pieces·µm(-2) , was synthesized. Copyright © 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Silicon-Encapsulated Hollow Carbon Nanofiber Networks as Binder-Free Anodes for Lithium Ion Battery

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Ding Nan

2014-01-01

Full Text Available Silicon-encapsulated hollow carbon nanofiber networks with ample space around the Si nanoparticles (hollow Si/C composites were successfully synthesized by dip-coating phenolic resin onto the surface of electrospun Si/PVA nanofibers along with the subsequent solidification and carbonization. More importantly, the structure and Si content of hollow Si/C composite nanofibers can be effectively tuned by merely varying the concentration of dip solution. As-synthesized hollow Si/C composites show excellent electrochemical performance when they are used as binder-free anodes for Li-ion batteries (LIBs. In particular, when the concentration of resol/ethanol solution is 3.0%, the product exhibits a large capacity of 841 mAh g−1 in the first cycle, prominent cycling stability, and good rate capability. The discharge capacity retention of it was ~90%, with 745 mAh g−1 after 50 cycles. The results demonstrate that the hollow Si/C composites are very promising as alternative anode candidates for high-performance LIBs.

Vortex-Induced Alignment of a Water Soluble Supramolecular Nanofiber Composed of an Amphiphilic Dendrimer

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Akihiko Tsuda

2013-06-01

Full Text Available We have synthesized a novel amphiphilic naphthalene imide bearing a cationic dendrimer wedge (NID. NID molecules in water self-assemble to form a two-dimensional ribbon, which further coils to give a linear supramolecular nanofiber. The sample solution showed linear dichroism (LD upon stirring of the solution, where NID nanofibers dominantly align at the center of vortex by hydrodynamic interaction with the downward torsional flows.

Improving effects of chitosan nanofiber scaffolds on osteoblast proliferation and maturation

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Ho MH

2014-09-01

Full Text Available Ming-Hua Ho,1,2 Mei-Hsiu Liao,3 Yi-Ling Lin,2 Chien-Hao Lai,3 Pei-I Lin,3 Ruei-Ming Chen2–4 1Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei, Taiwan; 2Cell Physiology and Molecular Image Research Center and Department of Anesthesiology, Wan Fang Hospital, 3Graduate Institute of Medical Sciences, Taipei Medical University, Taipei, Taiwan; 4Anesthetics and Toxicology Research Center, Taipei Medical University Hospital, Taipei, Taiwan Abstract: Osteoblast maturation plays a key role in regulating osteogenesis. Electrospun nanofibrous products were reported to possess a high surface area and porosity. In this study, we developed chitosan nanofibers and examined the effects of nanofibrous scaffolds on osteoblast maturation and the possible mechanisms. Macro- and micro observations of the chitosan nanofibers revealed that these nanoproducts had a flat surface and well-distributed fibers with nanoscale diameters. Mouse osteoblasts were able to attach onto the chitosan nanofiber scaffolds, and the scaffolds degraded in a time-dependent manner. Analysis by scanning electron microscopy further showed mouse osteoblasts adhered onto the scaffolds along the nanofibers, and cell–cell communication was also detected. Mouse osteoblasts grew much better on chitosan nanofiber scaffolds than on chitosan films. In addition, human osteoblasts were able to adhere and grow on the chitosan nanofiber scaffolds. Interestingly, culturing human osteoblasts on chitosan nanofiber scaffolds time-dependently increased DNA replication and cell proliferation. In parallel, administration of human osteoblasts onto chitosan nanofibers significantly induced osteopontin, osteocalcin, and alkaline phosphatase (ALP messenger (mRNA expression. As to the mechanism, chitosan nanofibers triggered runt-related transcription factor 2 mRNA and protein syntheses. Consequently, results of ALP-, alizarin red-, and von Kossa-staining analyses

Preparation of Amidoxime Polyacrylonitrile Chelating Nanofibers and Their Application for Adsorption of Metal Ions

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You-Lo Hsieh

2013-03-01

Full Text Available Polyacrylonitrile (PAN nanofibers were prepared by electrospinning and they were modified with hydroxylamine to synthesize amidoxime polyacrylonitrile (AOPAN chelating nanofibers, which were applied to adsorb copper and iron ions. The conversion of the nitrile group in PAN was calculated by the gravimetric method. The structure and surface morphology of the AOPAN nanofiber were characterized by a Fourier transform infrared spectrometer (FT-IR and a scanning electron microscope (SEM, respectively. The adsorption abilities of Cu2+ and Fe3+ ions onto the AOPAN nanofiber mats were evaluated. FT-IR spectra showed nitrile groups in the PAN were partly converted into amidoxime groups. SEM examination demonstrated that there were no serious cracks or sign of degradation on the surface of the PAN nanofibers after chemical modification. The adsorption capacities of both copper and iron ions onto the AOPAN nanofiber mats were higher than those into the raw PAN nanofiber mats. The adsorption data of Cu2+ and Fe3+ ions fitted particularly well with the Langmuir isotherm. The maximal adsorption capacities of Cu2+ and Fe3+ ions were 215.18 and 221.37 mg/g, respectively.

Electrospun propolis/polyurethane composite nanofibers for biomedical applications

Energy Technology Data Exchange (ETDEWEB)

Kim, Jeong In [Department of Bio-nano System Engineering, Chonbuk National University, Jeonju 561–756 (Korea, Republic of); Pant, Hem Raj, E-mail: hempant@jbnu.ac.kr [Department of Bio-nano System Engineering, Chonbuk National University, Jeonju 561–756 (Korea, Republic of); Department of Engineering Science and Humanities, Pulchowk Campus, Tribhuvan University, Kathmandu (Nepal); Research Institute for Next Generation, Kalanki, Kathmandu (Nepal); Sim, Hyun-Jaung [Department of Bioactive Material Science, Research Center of Bioactive Material, Chonbuk National University, Jeonju, Chonbuk (Korea, Republic of); Lee, Kang Min [Department of Molecular Biology, College of Natural Science, Chonbuk National University, Jeonju, 561–756 (Korea, Republic of); Kim, Cheol Sang, E-mail: chskim@jbnu.ac.kr [Department of Bio-nano System Engineering, Chonbuk National University, Jeonju 561–756 (Korea, Republic of)

2014-11-01

Tissue engineering requires functional polymeric membrane for adequate space for cell migration and attachment within the nanostructure. Therefore, biocompatible propolis loaded polyurethane (propolis/PU) nanofibers were successfully prepared using electrospinning of propolis/PU blend solution. Here, composite nanofibers were subjected to detailed analysis using electron microscopy, FT-IR spectroscopy, thermal gravimetric analysis (TGA), and mechanical properties and water contact angle measurement. FE-SEM images revealed that the composite nanofibers became point-bonded with increasing amounts of propolis in the blend due to its adhesive properties. Incorporation of small amount of propolis through PU matrix could improve the hydrophilicity and mechanical strength of the fibrous membrane. In order to assay the cytocompatibility and cell behavior on the composite scaffolds, fibroblast cells were seeded on the matrix. Results suggest that the incorporation of propolis into PU fibers could increase its cell compatibility. Moreover, composite nanofibers have effective antibacterial activity. Therefore, as-synthesized nanocomposite fibrous mat has great potentiality in wound dressing and skin tissue engineering. - Highlights: • Sufficient amount of propolis is simply loaded through PU fibers. • Propolis increases the hydrophilicity and mechanical properties of PU fibers. • Composite mat shows excellent antibacterial activity. • Small amount of propolis can enhance the cell compatibility of PU fibers.

Electrospun propolis/polyurethane composite nanofibers for biomedical applications

International Nuclear Information System (INIS)

Kim, Jeong In; Pant, Hem Raj; Sim, Hyun-Jaung; Lee, Kang Min; Kim, Cheol Sang

2014-01-01

Tissue engineering requires functional polymeric membrane for adequate space for cell migration and attachment within the nanostructure. Therefore, biocompatible propolis loaded polyurethane (propolis/PU) nanofibers were successfully prepared using electrospinning of propolis/PU blend solution. Here, composite nanofibers were subjected to detailed analysis using electron microscopy, FT-IR spectroscopy, thermal gravimetric analysis (TGA), and mechanical properties and water contact angle measurement. FE-SEM images revealed that the composite nanofibers became point-bonded with increasing amounts of propolis in the blend due to its adhesive properties. Incorporation of small amount of propolis through PU matrix could improve the hydrophilicity and mechanical strength of the fibrous membrane. In order to assay the cytocompatibility and cell behavior on the composite scaffolds, fibroblast cells were seeded on the matrix. Results suggest that the incorporation of propolis into PU fibers could increase its cell compatibility. Moreover, composite nanofibers have effective antibacterial activity. Therefore, as-synthesized nanocomposite fibrous mat has great potentiality in wound dressing and skin tissue engineering. - Highlights: • Sufficient amount of propolis is simply loaded through PU fibers. • Propolis increases the hydrophilicity and mechanical properties of PU fibers. • Composite mat shows excellent antibacterial activity. • Small amount of propolis can enhance the cell compatibility of PU fibers

SiC nanofibers grown by high power microwave plasma chemical vapor deposition

International Nuclear Information System (INIS)

Honda, Shin-ichi; Baek, Yang-Gyu; Ikuno, Takashi; Kohara, Hidekazu; Katayama, Mitsuhiro; Oura, Kenjiro; Hirao, Takashi

2003-01-01

Silicon carbide (SiC) nanofibers have been synthesized on Si substrates covered by Ni thin films using high power microwave chemical vapor deposition (CVD). Characterization using transmission electron microscopy (TEM) combined with electron energy-dispersive X-ray spectroscopy (EDX) revealed that the resultant fibrous nanostructures were assigned to β-SiC with high crystallinity. The formation of SiC nanofibers can be explained by the vapor liquid solid (VLS) mechanism in which precipitation of SiC occurs from the supersaturated Ni nanoparticle containing Si and C

Obtainment of silica nanofiber and its preliminary investigation and its effects as reinforcement in polymeric matrix

International Nuclear Information System (INIS)

Teixeira, R.S.; Oliveira, G.L.; Silva, F.D.C.; Teofilo, E. T.; Farias, R.C.; Menezes, R.R.

2016-01-01

Silica is widely used as fillers in polymers, and may confer flame retardant characteristics and improve mechanical properties. their use usually occurs as spherical nanoparticles or short fibers of. Studies using this reinforce in the form of nanofibers are promising. This analysis proposes to obtain silica nanofibers by blowspinning method in solution (SBS), and investigate its application in polymeric matrix. To synthesize the silica nanofibers it was used a precursor solution that has been subjected to SBS process and calcined for forming the silica layer. The DR-X indicated the obtainment of amorphous silica phase and SEM showed the the fibers are at the nanometer scale. Silica nanofibers were incorporated into filmogenic solution Polyamide 6. Preliminary results showed no improvement in mechanical properties. Future stages propose to verify that the surface chemical modification of silica nanofibers enables interaction charge / matrix. (author)

Spectroscopic study of nitrogen distribution in N-doped carbon nanotubes and nanofibers synthesized by catalytic ethylene-ammonia decomposition

Science.gov (United States)

Svintsitskiy, Dmitry A.; Kibis, Lidiya S.; Smirnov, Dmitry A.; Suboch, Arina N.; Stonkus, Olga A.; Podyacheva, Olga Yu.; Boronin, Andrei I.; Ismagilov, Zinfer R.

2018-03-01

Carbon and nitrogen species on the surface of carbon nanotubes (N-CNTs) and nanofibers (N-CNFs) were studied by X-ray absorption (XAS) and photoelectron spectroscopy (PES) including the analysis of nitrogen distribution over the depth of materials. The study was performed with a series of bamboo-like carbon nanotubes and nanofibers having the platelet-like and herringbone-like morphology. It was shown that the main nitrogen species in the composition of the studied materials are pyridine, pyrrole (and/or amino groups), graphite-like and oxidized states of nitrogen. In distinction to nanofibers, the bamboo-like nanotubes additionally contain molecular nitrogen encapsulated in the internal hollows. Spectral data for different depths of analysis were obtained by varying the energy of incident radiation. Such an approach revealed that N-CNTs are characterized by non-uniform distribution of chemically bound nitrogen species. Thus, nitrogen enrichment was observed on the external surface and in the internal arches of carbon nanotubes. Nitrogen enrichment in the subsurface region was found for N-CNFs, whereas the full depth analysis of N-distribution was limited by a large diameter of nanofibers.

Determination of morphology and properties of carbon nanofibers and carbon nanofiber polymer nanocomposites

Science.gov (United States)

Lawrence, Joseph G.

Vapor grown carbon nanofibers which resemble carbon nanotubes in structure and properties, have been extensively manufactured and investigated in recent years. Carbon nanofibers have been used for producing multifunctional materials due to their excellent properties and low cost of production. Since, commercially available vapor grown carbon nanofibers are subjected to different processing and post processing conditions, the morphology and properties of these nanofibers are not well-known. In this study, we focus on the characterization of the morphology and properties of these nanofibers and the polymer nanocomposites made using these nanofibers as reinforcements. The morphology of the nanofibers was studied employing high resolution Transmission Electron Microscopy (TEM) images. The analysis showed that the nanofibers consist primarily of conical nanofibers, but can contain a significant amount of bamboo nanofibers. Most of the conical nanofibers were found to consist of an ordered inner layer and a disordered outer layer, with the cone angle distribution of the inner layers indicating that these cannot have a stacked cone structure but are compatible with a cone-helix structure. Nanofibers that were heat treated to temperatures above 1,500°C undergo a structural transformation with the ordered inner layers changing from a cone-helix structure to a highly ordered multiwall stacked cone structure. Due to the complexity in the structure of these nanofibers, a novel method to study the elastic properties and corresponding morphology of individual nanofibers has been developed combining Atomic Force Microscopy (AFM), TEM and Focused Ion Beam (FIB) technology. Employing the developed method, the elastic modulus of individual nanofibers and their corresponding dimensions and morphology were determined. The dependence of elastic properties on the wall thickness and the orientation of graphene sheets in the nanofibers were studied. The elastic modulus of these

Facile synthesis of polypyrrole nanofiber and its enhanced electrochemical performances in different electrolytes

Directory of Open Access Journals (Sweden)

C. K. Das

2012-12-01

Full Text Available A porous nanocomposite based on polypyrrole (PPy and sodium alginate (SA has been synthesized by easy, inexpensive, eco-friendly method. As prepared nanocomposite showed fibrillar morphology in transmission electron microscopic (TEM analysis. The average diameter of ~100 nm for the nanofibers was observed from scanning electron microscopic (SEM analysis. As prepared nanofiber, was investigated as an electrode material for supercapacitor application in different aqueous electrolyte solutions. PPy nanofiber showed enhanced electrochemical performances in 1M KCl solution as compared to 1M Na2SO4 solution. Maximum specific capacitance of 284 F/g was found for this composite in 1 M KCl electrolyte. It showed 76% specific capacitance retention after 600 cycles in 1 M KCl solution. Electrochemical Impedance Spectra showed moderate capacitive behavior of the composite in both the electrolytes. Further PPy nanofiber demonstrated higher thermal stability as compared to pure PPy.

Nanofibers obtained by electrospinning of BaTiO3 particles dispersed in polyvinyl alcohol and ethylcellulose

Energy Technology Data Exchange (ETDEWEB)

Avila, Humar A.; Reboredo, Maria M.; Castro, Miriam; Parra, Rodrigo, E-mail: havila@fi.mdp.edu.ar [Instituto de Investigaciones en Ciencia y Tecnologia de Materiales - INTEMA, Consejo Nacional de Investigaciones Cientificas y Tecnicas - CONICET, Universidad Nacional de Mar del Plata - UNMdP, Mar del Plata (Argentina)

2013-11-01

Barium titanate particles (100-300 nm) synthesized by hydrothermal method were dispersed in both polyvinyl alcohol (PVA) and ethylcellulose (EC) solutions. These suspensions were processed by electrospinning. When no particles were added, homogeneous polymeric nanofibers were obtained. Under certain conditions, polymeric suspensions of barium titanate particles were electrospun generating polymeric fibers with BT particles. The effect of a surfactant was also assessed over the formation of nanofibers. The BaTiO{sub 3} particles synthesized by hydrothermal method were characterized by X-Ray diffraction (XRD), field emission-scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM) and Raman spectroscopy. Fibers were characterized by scanning electron microscopy (SEM). (author)

Carbon nanofibers wrapped with zinc oxide nano-flakes as promising electrode material for supercapacitors.

Science.gov (United States)

Pant, Bishweshwar; Park, Mira; Ojha, Gunendra Prasad; Park, Juhyeong; Kuk, Yun-Su; Lee, Eun-Jung; Kim, Hak-Yong; Park, Soo-Jin

2018-07-15

A combination of electrospinning technique and hydrothermal process was carried out to fabricate zinc oxide nano-flakes wrapped carbon nanofibers (ZnO/CNFs) composite as an effective electrode material for supercapacitor. The morphology of the as-synthesized composite clearly revealed that the carbon nanofibers were successfully wrapped with ZnO nano-flakes. The electrochemical performance of the as-synthesized nanocomposite electrode was evaluated by the cyclic voltammetry (CV), galvanostatic charge-discharge (GDC), and electrochemical impedance spectroscopy (EIS), and compared with the pristine ZnO nanofibers. It was found that the composite exhibited a higher specific capacitance (260 F/g) as compared to pristine ZnO NFs (118 F/g) at the scan rate of 5 mV/s. Furthermore, the ZnO/CNFs composite also exhibited good capacity retention (73.33%). The obtained results indicated great potential applications of ZnO/CNFs composite in developing energy storage devices with high energy and power densities. The present work might provide a new route for utilizing ZnO based composites for energy storage applications. Copyright © 2018 Elsevier Inc. All rights reserved.

Ideal asymmetric supercapacitors consisting of polyaniline nanofibers and graphene nanosheets with proper complementary potential windows

International Nuclear Information System (INIS)

Hung, P.-J.; Chang, K.-H.; Lee, Y.-F.; Hu, C.-C.; Lin, K.-M.

2010-01-01

Polyaniline (PANI) nanofibers are synthesized via a chemical method of rapid mixing for the application of asymmetric supercapacitors. The diameter and aspect ratio of PANI nanofibers is found to be controllable by varying the aniline/oxidant concentration ratio. The ideal capacitive responses of PANI nanofibers between 0.2 and 0.7 V (vs. Ag/AgCl) in concentrated acidic media are demonstrated by cyclic voltammetric (CV) and electrochemical impedance spectroscopic (EIS) analyses coupled with a schematic equivalent-circuit model. The morphologies and textures of nanofibers are examined by scanning electron microscopic (SEM), transmission electron microscopic (TEM) and Fourier transform infrared-attenuated total reflectance (FTIR-ATR) spectroscopic analyses. An aqueous asymmetric supercapacitor, consisting of a PANI nanofiber cathode and a graphene anode, with proper complementary potential windows is demonstrated in this work, which shows the device energy and power densities of 4.86 Wh kg -1 and 8.75 kW kg -1 , respectively.

Ideal asymmetric supercapacitors consisting of polyaniline nanofibers and graphene nanosheets with proper complementary potential windows

Energy Technology Data Exchange (ETDEWEB)

Hung, P.-J. [Department of Chemical Engineering, National Tsing Hua University, 101, Section 2, Kuang Fu Road, Hsin-Chu 30013, Taiwan (China); Chang, K.-H. [Department of Chemical Engineering, National Tsing Hua University, 101, Section 2, Kuang Fu Road, Hsin-Chu 30013, Taiwan (China); Department of Chemical Engineering, National Chung Cheng University, Chia-Yi 621, Taiwan (China); Lee, Y.-F. [Department of Chemical Engineering, National Tsing Hua University, 101, Section 2, Kuang Fu Road, Hsin-Chu 30013, Taiwan (China); Hu, C.-C., E-mail: cchu@che.nthu.edu.t [Department of Chemical Engineering, National Tsing Hua University, 101, Section 2, Kuang Fu Road, Hsin-Chu 30013, Taiwan (China); Lin, K.-M. [Department of Chemical Engineering, National Tsing Hua University, 101, Section 2, Kuang Fu Road, Hsin-Chu 30013, Taiwan (China)

2010-08-01

Polyaniline (PANI) nanofibers are synthesized via a chemical method of rapid mixing for the application of asymmetric supercapacitors. The diameter and aspect ratio of PANI nanofibers is found to be controllable by varying the aniline/oxidant concentration ratio. The ideal capacitive responses of PANI nanofibers between 0.2 and 0.7 V (vs. Ag/AgCl) in concentrated acidic media are demonstrated by cyclic voltammetric (CV) and electrochemical impedance spectroscopic (EIS) analyses coupled with a schematic equivalent-circuit model. The morphologies and textures of nanofibers are examined by scanning electron microscopic (SEM), transmission electron microscopic (TEM) and Fourier transform infrared-attenuated total reflectance (FTIR-ATR) spectroscopic analyses. An aqueous asymmetric supercapacitor, consisting of a PANI nanofiber cathode and a graphene anode, with proper complementary potential windows is demonstrated in this work, which shows the device energy and power densities of 4.86 Wh kg{sup -1} and 8.75 kW kg{sup -1}, respectively.

Methanol electro-oxidation on Pt/C modified by polyaniline nanofibers for DMFC applications

Energy Technology Data Exchange (ETDEWEB)

Zhiani, Mohammad; Rezaei, Behzad; Jalili, Jalal [Department of Chemistry, Isfahan University of Technology, Isfahan 84156-83111 (Iran)

2010-09-15

In the present study, in order to achieve an inexpensive tolerable anode catalyst for direct methanol fuel cell applications, a composite of polyaniline nanofibers and Pt/C nano-particles, identified by PANI/Pt/C, was prepared by in-situ electropolymerization of aniline and trifluoromethane sulfonic acid on glassy carbon. The effect of synthesized PANI nanofibers in methanol electrooxidation reaction was compared by bare Pt/C by different electrochemical methods such as; cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and chronoamperometry. Scanning electron microscopy (SEM) was also employed to morphological study of the modified catalyst layer. The test results reveal that introduction of PANI nanofibers within catalyst layer improves the catalyst activity in methanol oxidation, hinders and prevents catalyst from more poisoning by intermediate products of methanol oxidation and improves the mechanical properties of the catalyst layer. SEM images also indicate that PANI nanofibers placed between platinum particles and anchor platinum particles and alleviate the Pt migration during methanol electrooxidation. (author)

A simple approach for synthesis, characterization and bioactivity of bovine bones to fabricate the polyurethane nanofiber containing hydroxyapatite nanoparticles

Directory of Open Access Journals (Sweden)

F. A. Sheikh

2012-01-01

Full Text Available In the present study, we had introduced polyurethane (PU nanofibers that contain hydroxyapatite (HAp nanoparticles (NPs as a result of an electrospinning process. A simple method that does not depend on additional foreign chemicals had been employed to synthesize HAp NPs through the calcination of bovine bones. Typically, a colloidal gel consisting of HAp/PU had been electrospun to form nanofibers. In this communication, physiochemical aspects of prepared nanofibers were characterized by FE-SEM, TEM and TEM-EDS, which confirmed that nanofibers were well-oriented and good dispersion of HAp NPs, over the prepared nanofibers. Parameters, affecting the utilization of the prepared nanofibers in various nano-biotechnological fields have been studied; for instance, the bioactivity of the produced nanofiber mats was investigated while incubating in simulated body fluid (SBF. The results from incubation of nanofibers, indicated that incorporation of HAp strongly activates the precipitation of the apatite-like particles, because of the HAp NPs act as seed, that accelerate crystallization of the biological HAp from the utilized SBF.

Pretreatment assisted synthesis and characterization of cellulose nanocrystals and cellulose nanofibers from absorbent cotton.

Science.gov (United States)

Abu-Danso, Emmanuel; Srivastava, Varsha; Sillanpää, Mika; Bhatnagar, Amit

2017-09-01

In this work, cellulose nanocrystals (CNCs) and cellulose nanofibers (CNFs) were synthesized from absorbent cotton. Two pretreatments viz. dewaxing and bleaching with mild alkali were applied to the precursor (cotton). Acid hydrolysis was conducted with H 2 SO 4 and dissolution of cotton was achieved with a mixture of NaOH-thiourea-urea-H 2 O at -3°C. Synthesized cellulose samples were characterized using FTIR, XRD, SEM, BET, and zeta potential. It seems that synthesis conditions contributed to negative surface charge on cellulose samples and CNCs had the higher negative surface charge compared to CNFs. Furthermore, BET surface area, pore volume and pore diameter of CNCs were found to be higher as compared to CNFs. The dewaxed cellulose nanofibers (CNF D) had a slightly higher BET surface area (0.47m 2 /g) and bigger pore diameter (59.87Å) from attenuated contraction compared to waxed cellulose nanofibers (CNFW) (0.38m 2 /g and 44.89Å). The XRD of CNCs revealed a semi-crystalline structure and the dissolution agents influenced the crystallinity of CNFs. SEM images showed the porous nature of CNFs, the flaky nature and the nano-sized width of CNCs. Synthesized CNF D showed a better potential as an adsorbent with an average lead removal efficiency of 91.49% from aqueous solution. Copyright © 2017 Elsevier B.V. All rights reserved.

Synthesis of nitrogen-doped porous carbon nanofibers as an efficient electrode material for supercapacitors.

Science.gov (United States)

Chen, Li-Feng; Zhang, Xu-Dong; Liang, Hai-Wei; Kong, Mingguang; Guan, Qing-Fang; Chen, Ping; Wu, Zhen-Yu; Yu, Shu-Hong

2012-08-28

Supercapacitors (also known as ultracapacitors) are considered to be the most promising approach to meet the pressing requirements of energy storage. Supercapacitive electrode materials, which are closely related to the high-efficiency storage of energy, have provoked more interest. Herein, we present a high-capacity supercapacitor material based on the nitrogen-doped porous carbon nanofibers synthesized by carbonization of macroscopic-scale carbonaceous nanofibers (CNFs) coated with polypyrrole (CNFs@polypyrrole) at an appropriate temperature. The composite nanofibers exhibit a reversible specific capacitance of 202.0 F g(-1) at the current density of 1.0 A g(-1) in 6.0 mol L(-1) aqueous KOH electrolyte, meanwhile maintaining a high-class capacitance retention capability and a maximum power density of 89.57 kW kg(-1). This kind of nitrogen-doped carbon nanofiber represents an alternative promising candidate for an efficient electrode material for supercapacitors.

Fabrication of electrospun ZnMn2O4 nanofibers as anode material for lithium-ion batteries

International Nuclear Information System (INIS)

Luo, Lei; Qiao, Hui; Chen, Ke; Fei, Yaqian; Wei, Qufu

2015-01-01

Highlights: • ZnMn 2 O 4 nanofibers were successfully synthesized by a facile electrospinning and calcination method for lithium-ion batteries. • The as-prepared ZnMn 2 O 4 nanofibers, containing PVP and PAN with ratio of 1:9, exhibited a high initial discharge capacity of 1274 mAh g −1 , and the stabilized capacity was as high as 603 mAh g −1 after 60 cycles at a current density of 50 mA g −1 . • The as-prepared ZnMn 2 O 4 anode material showed good lithium storage performances and excellent rate capability and can be a promising electrode material for lithium-ion batteries in the future. - Abstract: In this paper, ZnMn 2 O 4 nanofibers were synthesized by a facile electrospinning and calcination method. Electrochemical properties of the nanofiber anode material for lithium-ion batteries were investigated. The as-prepared ZnMn 2 O 4 nanofibers, containing PVP and PAN with ratio of 1:9, exhibited a high initial discharge capacity of 1274 mAh g −1 , and the stabilized capacity was as high as 603 mAh g −1 after 60 cycles at a current density of 50 mA g −1 . Besides the high specific capacity and good cyclability, the electrode also showed good rate capability. Even at 2000 mA g −1 , the electrode could deliver a capacity of as high as 352 mAh g −1 . The results suggest a promising application of the electrospun ZnMn 2 O 4 nanofibers as anode material for lithium-ion batteries

Morphological Effects of HA on the Cell Compatibility of Electrospun HA/PLGA Composite Nanofiber Scaffolds

Directory of Open Access Journals (Sweden)

Adnan Haider

2014-01-01

Full Text Available Tissue engineering is faced with an uphill challenge to design a platform with appropriate topography and suitable surface chemistry, which could encourage desired cellular activities and guide bone tissue regeneration. To develop such scaffolds, composite nanofiber scaffolds of nHA and sHA with PLGA were fabricated using electrospinning technique. nHA was synthesized using precipitation method, whereas sHA was purchased. The nHA and sHA were suspended in PLGA solution separately and electrospun at optimized electrospinning parameters. The composite nanofiber scaffolds were characterized by FE-SEM, EDX analysis, TEM, XRD analysis, FTIR, and X-ray photoelectron. The potential of the HA/PLGA composite nanofiber as bone scaffolds in terms of their bioactivity and biocompatibility was assessed by culturing the osteoblastic cells onto the composite nanofiber scaffolds. The results from in vitro studies revealed that the nHA/PLGA composite nanofiber scaffolds showed higher cellular adhesion, proliferation, and enhanced osteogenesis performance, along with increased Ca+2 ions release compared to the sHA/PLGA composite nanofiber scaffolds and pristine PLGA nanofiber scaffold. The results show that the structural dependent property of HA might affect its potential as bone scaffold and implantable materials in regenerative medicine and clinical tissue engineering.

The photocatalytic properties of hollow (GaN){sub 1-x}(ZnO){sub x} composite nanofibers synthesized by electrospinning

Energy Technology Data Exchange (ETDEWEB)

Wang, Ding; Zhang, Minglu; Zhuang, Huaijuan; Chen, Xu [College of Materials Science and Engineering, University of Shanghai for Science & Technology, Shanghai, 200093 (China); Wang, Xianying, E-mail: Xianyingwang@usst.edu.cn [College of Materials Science and Engineering, University of Shanghai for Science & Technology, Shanghai, 200093 (China); Zheng, Xuejun, E-mail: zhengxuejun@xtu.edu.cn [School of Mechanical Engineering, Xiangtan University, Xiangtan, 411105 (China); Key Laboratory of Welding Robot and Application Technology of Hunan Province, Xiangtan University, Xiangtan, 411105 (China); Yang, Junhe [College of Materials Science and Engineering, University of Shanghai for Science & Technology, Shanghai, 200093 (China)

2017-02-28

Highlights: • (GaN){sub 1-x}(ZnO){sub x} composite nanofibers were obtained by electrospinning method. • Phase transition from ZnGa{sub 2}O{sub 4} to (GaN){sub 1-x}(ZnO){sub x} under NH{sub 3} was observed. • Hollow and porous structure was confirmed by SEM and TEM investigation. • GaN:ZnO with optimal ratio of 1:2 displayed highest photocatalytic activity. - Abstract: (GaN){sub 1-x}(ZnO){sub x} composite nanofibers with hollow structure were prepared by initial electrospinning, and the subsequent calcination and nitridation. The structure and morphology characteristics of samples were investigated by X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), energy dispersive X-ray spectroscopy (EDS) and transmission electron microscopy (TEM). The characterization results showed the phase transition from ZnGa{sub 2}O{sub 4} to (GaN){sub 1-x}(ZnO){sub x} solid-solution under ammonia atmosphere. The preparation conditions were explored and the optimum nitridation temperature and holding time are 750 °C and 2 h, respectively. The photocatalytic properties of (GaN){sub 1-x}(ZnO){sub x} with different Ga:Zn atomic ratios were investigated by degrading Rhodamine B under the visible light irradiation. The photocatalytic activity sequence is (GaN){sub 1−x}(ZnO){sub x} (Ga:Zn = 1:2) > (GaN){sub 1−x}(ZnO){sub x} (Ga:Zn = 1:3) > ZnO nanofibers > (GaN){sub 1−x}(ZnO){sub x} (Ga:Zn = 1:4) > (GaN){sub 1−x}(ZnO){sub x} (Ga:Zn = 1:1). The photocatalytic mechanism of the (GaN){sub 1−x}(ZnO){sub x} hollow nanofibers was further studied by UV–vis diffuse reflectance spectra. The excellent photocatalytic performance of (GaN){sub 1−x}(ZnO){sub x} hollow nanofibers was attributed to the narrow band gap and high surface area of porous nanofibers with hollow structure.

Superior lithium storage performance of hierarchical porous vanadium pentoxide nanofibers for lithium ion battery cathodes

Energy Technology Data Exchange (ETDEWEB)

Yan, Bo [Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, School of Materials Science and Technology, China University of Geosciences, Beijing 100083 (China); Energy & Materials Engineering Centre, College of Physics and Materials Science, Tianjin Normal University, Tianjin 300387 (China); National Key Laboratory of Power Sources, Tianjin Institute of Power Sources, Tianjin 300381 (China); Li, Xifei, E-mail: xfli2011@hotmail.com [Energy & Materials Engineering Centre, College of Physics and Materials Science, Tianjin Normal University, Tianjin 300387 (China); Bai, Zhimin, E-mail: zhimibai@cugb.edu.cn [Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, School of Materials Science and Technology, China University of Geosciences, Beijing 100083 (China); Li, Minsi [Department of Chemistry, University of Science and Technology of China, Hefei, Anhui 230026 (China); Dong, Lei; Xiong, Dongbin [Energy & Materials Engineering Centre, College of Physics and Materials Science, Tianjin Normal University, Tianjin 300387 (China); Li, Dejun, E-mail: dejunli@mail.tjnu.edu.cn [Energy & Materials Engineering Centre, College of Physics and Materials Science, Tianjin Normal University, Tianjin 300387 (China)

2015-06-15

Highlights: • Hierarchical porous vanadium pentoxide nanofibers were synthesized by electrospinning. • V{sub 2}O{sub 5} nanofibers showed much enhanced lithium storage performance. • Kinetics process of electrospinning V{sub 2}O{sub 5} nanofibers was studied by means of EIS for the first time. • Strategies to enhance the electrochemical performance of V{sub 2}O{sub 5} electrode were concluded. - Abstract: The hierarchical V{sub 2}O{sub 5} nanofibers cathode materials with diameter of 200–400 nm are successfully synthesized via an electrospinning followed by annealing. Powder X-ray diffraction (XRD) pattern confirms the formation of phase-pure product. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) obviously display the hierarchical porous nanofibers constructed by attached tiny vanadium oxide nanoplates. Electrochemical behavior of the as-prepared product is systematically studied using galvanostatic charge/discharge testing, cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS). It turns out that in comparison to the commercial V{sub 2}O{sub 5} and other unique nanostructured materials in the literature, our V{sub 2}O{sub 5} nanofibers show much enhanced lithium storage capacity, improved cyclic stability, and higher rate capability. After 100 cycles at a current density of 800 mA g{sup −1}, the specific capacity of the V{sub 2}O{sub 5} nanofibers retain 133.9 mAh g{sup −1}, corresponding to high capacity retention of 96.05%. More importantly, the EIS at various discharge depths clearly reveal the kinetics process of the V{sub 2}O{sub 5} cathode reaction with lithium. Based on our results, the possible approach to improve the specific capacity and rate capability of the V{sub 2}O{sub 5} cathode material is proposed. It is expected that this study could accelerate the development of V{sub 2}O{sub 5} cathode in rechargeable lithium ion batteries.

Regulating drug release from pH- and temperature-responsive electrospun CTS-g-PNIPAAm/poly(ethylene oxide) hydrogel nanofibers

International Nuclear Information System (INIS)

Yuan, Huihua; Li, Biyun; Liang, Kai; Lou, Xiangxin; Zhang, Yanzhong

2014-01-01

Temperature- and pH-responsive polymers have been widely investigated as smart drug release systems. However, dual-sensitive polymers in the form of nanofibers, which is advantageous in achieving rapid transfer of stimulus to the smart polymeric structures for regulating drug release behavior, have rarely been explored. In this study, chitosan-graft-poly(N-isopropylacrylamide) (CTS-g-PNIPAAm) copolymer was synthesized by using 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) and N-hydroxy succinimide (NHS) as grafting agents to graft carboxyl-terminated PNIPAAm (PNIPAAm-COOH) chains onto the CTS biomacromolecules, and then CTS-g-PNIPAAm with or without bovine serum albumin (BSA) was fabricated into nanofibers through electrospinning using poly(ethylene oxide) (PEO, 10 wt%) as a fiber-forming facilitating additive. The BSA laden CTS-g-PNIPAAm/PEO hydrogel nanofibers were tested to determine their drug release profiles by varying pH and temperature. Finally, cytotoxicity of the CTS-g-PNIPAAm/PEO hydrogel nanofibers was evaluated by assaying the L929 cell proliferation using the MTT method. It was found that the synthesized CTS-g-PNIPAAm possessed a temperature-induced phase transition and lower critical solution temperature (LCST) at 32° C in aqueous solutions. The rate of BSA release could be well modulated by altering the environmental pH and temperature of the hydrogel nanofibers. The CTS-g-PNIPAAm/PEO hydrogel nanofibers supported L929 cell growth, indicative of appropriate cytocompatibility. Our current work could pave the way towards developing multi-stimuli responsive nanofibrous smart materials for potential applications in the fields of drug delivery and tissue engineering. (paper)

Characterization of Plasma Synthesized Vertical Carbon Nanofibers for Nanoelectronics Applications

Science.gov (United States)

Lee, Jaesung; Feng, Philip X.-L.; Kaul, Anupama B.

2013-01-01

We report on the material characterization of carbon nanofibers (CNFs) which are assembled into a three-dimensional (3D) configuration for making new nanoelectromechanical systems (NEMS). High-resolution scanning electron microscopy (SEM) and x-ray electron dispersive spectroscopy (XEDS) are employed to decipher the morphology and chemical compositions of the CNFs at various locations along individual CNFs grown on silicon (Si) and refractory nitride (NbTiN) substrates, respectively. The measured characteristics suggest interesting properties of the CNF bodies and their capping catalyst nanoparticles, and growth mechanisms on the two substrates. Laser irradiation on the CNFs seems to cause thermal oxidation and melting of catalyst nanoparticles. The structural morphology and chemical compositions of the CNFs revealed in this study should aid in the applications of the CNFs to nanoelectronics and NEMS.

Ultra long single crystalline Na{sub 0.3}V{sub 2}O{sub 5} nanofibers/nanorings synthesized by a facile one pot green approach and their lithium storage behavior

Energy Technology Data Exchange (ETDEWEB)

Nagaraju, Ganganagappa, E-mail: nagarajugn@rediffmail.com [Jain University, Bangalore (India). Center for Nano and Material Sciences

2013-10-15

In this work, a simple one step hydrothermal method to synthesize Na{sub 0.3}V{sub 2}O{sub 5} nanofibers/nanorings without using any surfactant at 200 Degree-Sign C in 3-5 days is reported. The products were characterized by X-ray diffractometry (XRD), Fourier transform infrared spectroscopy (FTIR), UV-Vis spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM) and electrochemical discharge-charge test for lithium ion batteries. XRD patterns showed that, at 200 Degree-Sign C for 2 and 3-4 days, Na{sub 0.3}V{sub 2}O{sub 5.} Bullet 1.5H{sub 2}O belts and Na{sub 0.3}V{sub 2}O{sub 5} nanofibers/rings were formed, respectively. The FTIR spectrum revealed peaks at 1003 and 956 cm{sup -1} assigned respectively to V{sup 5+}=O and V{sup 4+}=O. The UV-Vis spectrum showed maximum absorbance at 404 nm (3.07 eV). TEM analyses revealed a large quantity of fibers 70-100 nm thick and 20-90 {mu}m long, and rings with diameters of ca. 20 Greek-Small-Letter-Mu m and thickness of 70-150 nm. The nanofibers/rings exhibited an initial discharge specific capacity of 182 mAh g{sup -1} and a stabilized capacity of 179 mAh g{sup -1} even after 50 cycles. A possible mechanism for ring formation is discussed. (author)

Influence of temperature on the photodegradation process using Ag-doped TiO2nanostructures: Negative impact with the nanofibers

DEFF Research Database (Denmark)

Barakata, Nasser A.M.; Kanjwal, Muzafar Ahmad; Chronakis, Ioannis S.

In this study, the influence of the temperature on the photodegradation process using Ag-doped TiO2 nanostructures was investigated. Two morphologies were used; nanoparticles and nanofibers. The nanofibers were synthesized by electrospinning of a sol–gel consisting of titanium isopropoxide, silver...... nitrate and poly(vinyl acetate). The silver nitrate amount was changed to produce nanofibers having different silver contents. Typically, sol–gels containing 0.5, 1.0, 1.5, 2.0 and 2.5 wt% silver nitrate were utilized. Calcination of the electrospun mats at 700 °C led to produce well morphology Ag...

Double emulsion electrospun nanofibers as a growth factor delivery vehicle for salivary gland regeneration

Science.gov (United States)

Foraida, Zahraa I.; Sharikova, Anna; Peerzada, Lubna N.; Khmaladze, Alexander; Larsen, Melinda; Castracane, James

2017-08-01

Sustained delivery of growth factors, proteins, drugs and other biologically active molecules is necessary for tissue engineering applications. Electrospun fibers are attractive tissue engineering scaffolds as they partially mimic the topography of the extracellular matrix (ECM). However, they do not provide continuous nourishment to the tissue. In search of a biomimetic scaffold for salivary gland tissue regeneration, we previously developed a blend nanofiber scaffold composed of the protein elastin and the synthetic polymer polylactic-co-glycolic acid (PLGA). The nanofiber scaffold promoted in vivo-like salivary epithelial cell tissue organization and apicobasal polarization. However, in order to enhance the salivary cell proliferation and biomimetic character of the scaffold, sustained growth factor delivery is needed. The composite nanofiber scaffold was optimized to act as a growth factor delivery system using epidermal growth factor (EGF) as a model protein. The nanofiber/EGF hybrid nanofibers were synthesized by double emulsion electrospinning where EGF is emulsified within a water/oil/water (w/o/w) double emulsion system. Successful incorporation of EGF was confirmed using Raman spectroscopy. EGF release profile was characterized using enzyme-linked immunosorbent assay (ELIZA) of the EGF content. Double emulsion electrospinning resulted in slower release of EGF. We demonstrated the potential of the proposed double emulsion electrospun nanofiber scaffold for the delivery of growth factors and/or drugs for tissue engineering and pharmaceutical applications.

Fluorescent Nanocomposite of Embedded Ceria Nanoparticles in Crosslinked PVA Electrospun Nanofibers

Directory of Open Access Journals (Sweden)

Nader Shehata

2016-06-01

Full Text Available This paper introduces a new fluorescent nanocomposite of electrospun biodegradable nanofibers embedded with optical nanoparticles. In detail, this work introduces the fluorescence properties of PVA nanofibers generated by the electrospinning technique with embedded cerium oxide (ceria nanoparticles. Under near-ultra violet excitation, the synthesized nanocomposite generates a visible fluorescent emission at 520 nm, varying its intensity peak according to the concentration of in situ embedded ceria nanoparticles. This is due to the fact that the embedded ceria nanoparticles have optical tri-valiant cerium ions, associated with formed oxygen vacancies, with a direct allowed bandgap around 3.5 eV. In addition, the impact of chemical crosslinking of the PVA on the fluorescence emission is studied in both cases of adding ceria nanoparticles in situ or of a post-synthesis addition via a spin-coating mechanism. Other optical and structural characteristics such as absorbance dispersion, direct bandgap, FTIR spectroscopy, and SEM analysis are presented. The synthesized optical nanocomposite could be helpful in different applications such as environmental monitoring and bioimaging.

Ammonia gas sensors based on In2O3/PANI hetero-nanofibers operating at room temperature

Directory of Open Access Journals (Sweden)

Qingxin Nie

2016-09-01

Full Text Available Indium nitrate/polyvinyl pyrrolidone (In(NO33/PVP composite nanofibers were synthesized via electrospinning, and then hollow structure indium oxide (In2O3 nanofibers were obtained through calcination with PVP as template material. In situ polymerization was used to prepare indium oxide/polyaniline (In2O3/PANI composite nanofibers with different mass ratios of In2O3 to aniline. The structure and morphology of In(NO33/PVP, In2O3/PANI composite nanofibers and pure PANI were investigated by scanning electron microscopy (SEM, Fourier transform infrared spectroscopy (FTIR, X-ray diffraction (XRD, transmission electron microscopy (TEM and current–voltage (I–V measurements. The gas sensing properties of these materials towards NH3 vapor (100 to 1000 ppm were measured at room temperature. The results revealed that the gas sensing abilities of In2O3/PANI composite nanofibers were better than pure PANI. In addition, the mass ratio of In2O3 to aniline and the p–n heterostructure between In2O3 and PANI influences the sensing performance of the In2O3/PANI composite nanofibers. In this paper, In2O3/PANI composite nanofibers with a mass ratio of 1:2 exhibited the highest response values, excellent selectivity, good repeatability and reversibility.

ZnO-PLLA Nanofiber Nanocomposite for Continuous Flow Mode Purification of Water from Cr(VI

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T. Burks

2015-01-01

Full Text Available Nanomaterials of ZnO-PLLA nanofibers have been used for the adsorption of Cr(VI as a prime step for the purification of water. The fabrication and application of the flexible ZnO-PLLA nanofiber nanocomposite as functional materials in this well-developed architecture have been achieved by growing ZnO nanorod arrays by chemical bath deposition on synthesized electrospun poly-L-lactide nanofibers. The nanocomposite material has been tested for the removal and regeneration of Cr(IV in aqueous solution under a “continuous flow mode” by studying the effects of pH, contact time, and desorption steps. The adsorption of Cr(VI species in solution was greatly dependent upon pH. SEM micrographs confirmed the successful fabrication of the ZnO-PLLA nanofiber nanocomposite. The adsorption and desorption of Cr(VI species were more likely due to the electrostatic interaction between ZnO and Cr(VI ions as a function of pH. The adsorption and desorption experiments utilizing the ZnO-PLLA nanofiber nanocomposite have appeared to be an effective nanocomposite in the removal and regeneration of Cr(VI species.

Synthesis of Antibacterial Silver–Poly(ɛ-caprolactone-Methacrylic Acid Graft Copolymer Nanofibers and Their Evaluation as Potential Wound Dressing

Directory of Open Access Journals (Sweden)

Mohammed A. Al-Omair

2015-08-01

Full Text Available Electrospun polycaprolacyone/polymethacrylic acid graft copolymer nanofibers (PCL/MAA containing silver nanoparticles (AgNPs were synthesized for effective wound disinfection. Surface morphology, AgNPs content, water uptake of electrospun PCL/MAA graft copolymer nanofibers without and with AgNPs, and levels of AgNPs leaching from the nanofibers in water as well as antimicrobial efficacy were studied. Scanning electron microscope images revealed that AgNPs dispersed well in PCL/MAA copolymer nanofibers with mean fiber diameters in the range of 200–579 nm and the fiber uniformity and diameter were not affected by the AgNPs. TEM images showed that AgNPs are present in/on the electrospun PCL/MAA graft copolymer nanofibers. The diameter of the electrospun nanofibers containing AgNPs was in the range of 200–579 nm, however, the diameter of AgNPs was within the range of 20–50 nm and AgNPs were observed to be spherical in shape. The PCL/MAA copolymer nanofibers showed a good hydrophilic property and the nanofibers containing AgNPs had excellent antimicrobial activity against the Gram-negative bacteria Escherichia coli and Pseudomonas aeruginosa, and against the Gram-positive bacteria Bacillus thuringiensis and Staphylococcus aureus, with a clear inhibition zone with a diameter between 22 and 53 mm. Moreover, electrospun PCL/MAA copolymer nanofibers sustained the release of AgNPs into water over 72 h.

Preparation of In2O3 ceramic nanofibers by electrospinning and their optical properties

International Nuclear Information System (INIS)

Zhang Yanfei; Li Jiayan; Li Qin; Zhu Ling; Liu Xiangdong; Zhong Xinghua; Meng Jian; Cao Xueqiang

2007-01-01

Electrospinning was employed to fabricate polymer-ceramic composite fibers from solutions containing polyvinyl pyrrolidone (PVP) and In(NO 3 ) 3 .412H 2 O. Upon firing the composite fibers at 800 deg. C, In 2 O 3 fibers with diameters ranging from 200 to 400nm were synthesized. This indium oxide calcined at 800 deg. C is a body-centered cubic cell. The photoluminescence (PL) properties of the as-formed In 2 O 3 nanofibers were investigated. The In 2 O 3 nanofibers show a strong PL emission in the ultraviolet (UV) region under shorter UV light irradiation

Processing and Structure of Carbon Nanofiber Paper

Directory of Open Access Journals (Sweden)

Zhongfu Zhao

2009-01-01

Full Text Available A unique concept of making nanocomposites from carbon nanofiber paper was explored in this study. The essential element of this method was to design and manufacture carbon nanofiber paper with well-controlled and optimized network structure of carbon nanofibers. In this study, carbon nanofiber paper was prepared under various processing conditions, including different types of carbon nanofibers, solvents, dispersants, and acid treatment. The morphologies of carbon nanofibers within the nanofiber paper were characterized with scanning electron microscopy (SEM. In addition, the bulk densities of carbon nanofiber papers were measured. It was found that the densities and network structures of carbon nanofiber paper correlated to the dispersion quality of carbon nanofibers within the paper, which was significantly affected by papermaking process conditions.

Electrospun Gallium Nitride Nanofibers

International Nuclear Information System (INIS)

Melendez, Anamaris; Morales, Kristle; Ramos, Idalia; Campo, Eva; Santiago, Jorge J.

2009-01-01

The high thermal conductivity and wide bandgap of gallium nitride (GaN) are desirable characteristics in optoelectronics and sensing applications. In comparison to thin films and powders, in the nanofiber morphology the sensitivity of GaN is expected to increase as the exposed area (proportional to the length) increases. In this work we present electrospinning as a novel technique in the fabrication of GaN nanofibers. Electrospinning, invented in the 1930s, is a simple, inexpensive, and rapid technique to produce microscopically long ultrafine fibers. GaN nanofibers are produced using gallium nitrate and dimethyl-acetamide as precursors. After electrospinning, thermal decomposition under an inert atmosphere is used to pyrolyze the polymer. To complete the preparation, the nanofibers are sintered in a tube furnace under a NH 3 flow. Both scanning electron microscopy and profilometry show that the process produces continuous and uniform fibers with diameters ranging from 20 to a few hundred nanometers, and lengths of up to a few centimeters. X-ray diffraction (XRD) analysis shows the development of GaN nanofibers with hexagonal wurtzite structure. Future work includes additional characterization using transmission electron microscopy and XRD to understand the role of precursors and nitridation in nanofiber synthesis, and the use of single nanofibers for the construction of optical and gas sensing devices.

Synthesis and upconversion luminescence properties of YF{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers derived from Y{sub 2}O{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers

Energy Technology Data Exchange (ETDEWEB)

Li Dan; Dong Xiangting, E-mail: dongxiangting888@163.com; Yu Wensheng; Wang Jinxian; Liu Guixia [Changchun University of Science and Technology, Key Laboratory of Applied Chemistry and Nanotechnology at Universities of Jilin Province (China)

2013-06-15

YF{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers were successfully fabricated via fluorination of the relevant Y{sub 2}O{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers which were obtained by calcining the electrospun PVP/[Y(NO{sub 3}){sub 3} + Yb(NO{sub 3}){sub 3} + Er(NO{sub 3}){sub 3}] composite nanofibers. The morphology and properties of the products were investigated in detail by X-ray diffraction, scanning electron microscope, transmission electron microscope, and fluorescence spectrometer. YF{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers were pure orthorhombic phase with space group Pnma and were hollow-centered structure with mean diameter of 174 {+-} 22 nm, and YF{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers are composed of nanoparticles with size in the range of 30-60 nm. Upconversion emission spectrum analysis manifested that YF{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers emitted strong green and weak red upconversion emissions centering at 523, 545, and 654 nm, respectively. The green and red emissions were, respectively, originated from {sup 2}H{sub 11/2}/{sup 4}S{sub 3/2} {yields} {sup 4}I{sub 15/2} and {sup 4}F{sub 9/2} {yields} {sup 4}I{sub l5/2} energy levels transitions of the Er{sup 3+} ions. Moreover, the emitting colors of YF{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers were located in the green region in CIE chromaticity coordinates diagram. This preparation technique could be applied to prepare other rare earth fluoride upconversion luminescence hollow nanofibers.Graphical AbstractYF{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers with orthorhombic structure were synthesized by fluorination of the electrospun Y{sub 2}O{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers via a double-crucible method using NH{sub 4}HF{sub 2} as fluorinating agent. The mean diameter of YF{sub 3}:Yb{sup 3+}/Er{sup 3+} hollow nanofibers was 174 {+-} 22 nm. The fluorination method we proposed here has been proved to be an important method, as it can not only

Preparation and Characterization of Gelatin Nanofibers Containing Silver Nanoparticles

Science.gov (United States)

Jeong, Lim; Park, Won Ho

2014-01-01

Ag nanoparticles (NPs) were synthesized in formic acid aqueous solutions through chemical reduction. Formic acid was used for a reducing agent of Ag precursor and solvent of gelatin. Silver acetate, silver tetrafluoroborate, silver nitrate, and silver phosphate were used as Ag precursors. Ag+ ions were reduced into Ag NPs by formic acid. The formation of Ag NPs was characterized by a UV-Vis spectrophotometer. Ag NPs were quickly generated within a few minutes in silver nitrate (AgNO3)/formic acid solution. As the water content of formic acid aqueous solution increased, more Ag NPs were generated, at a higher rate and with greater size. When gelatin was added to the AgNO3/formic acid solution, the Ag NPs were stabilized, resulting in smaller particles. Moreover, gelatin limits further aggregation of Ag NPs, which were effectively dispersed in solution. The amount of Ag NPs formed increased with increasing concentration of AgNO3 and aging time. Gelatin nanofibers containing Ag NPs were fabricated by electrospinning. The average diameters of gelatin nanofibers were 166.52 ± 32.72 nm, but these decreased with the addition of AgNO3. The average diameters of the Ag NPs in gelatin nanofibers ranged between 13 and 25 nm, which was confirmed by transmission electron microscopy (TEM). PMID:24758929

Free-standing, well-aligned ordered mesoporous carbon nanofibers on current collectors for high-power micro-supercapacitors.

Science.gov (United States)

Kang, Eunae; Jeon, Gumhye; Kim, Jin Kon

2013-07-21

The mesoporous carbon nanofiber arrays that stand on carbon-gold double-layer current collectors are synthesized by self-assembly of a PS-b-PEO copolymer and resol in AAO templates for a high-power micro-supercapacitor at high current densities.

The Novel Synthesis Route for 3-Poly (vinylbenzyl-5,5-Dimethylimidazolidine-2,4-dione Nanofibers and Study of Its Antibacterial Properties

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Bozorgmehr Maddah

2016-01-01

Full Text Available As part of our ongoing interest in exploring the synthesis of antibacterial agent, we report an efficient, mild, one pot and chemoselective procedure for preparation of 3-poly (vinylbenzyl-5,5-dimethylimidazolidine-2,4-dione as a antimicrobial agent from poly(vinylbenzyl chloride and 5,5-dimethylhydantoin in the presence of a base in DMF as a solven. The FT-IR technique and melting point confirmed the desire product. Then, 3-poly (vinylbenzyl-5,5-dimethylimidazolidine-2,4-dione nanofibers was produced by electrospinning process. To confirm the nanofiber materials, SEM image was applied. Then, these nanofibers were, chlorinated with sodium hypochlorite. Finally, the antibacterial activity of synthesized nanofibers was evaluated by against Staphylococcus aureus as gram-positive bacteria and Escherichia coli as gram-negative bacteria. The results from culture media and halo diameters of nanofibers showed that high biocidal effect of fibers against these bacteria. These nanofibes could be used in order to construct filters needed to clean and disinfect drinking water in emergency.

Effect of fiber geometry on macroscale friction of ordered low-density polyethylene nanofiber arrays.

Science.gov (United States)

Lee, Dae Ho; Kim, Yongkwan; Fearing, Ronald S; Maboudian, Roya

2011-09-06

Ordered low-density polyethylene (LDPE) nanofiber arrays are fabricated from silicon nanowire (SiNW) templates synthesized by a simple wet-chemical process based on metal-assisted electroless etching combined with colloidal lithography. The geometrical effect of nanofibrillar structures on their macroscale friction is investigated over a wide range of diameters and lengths under the same fiber density. The optimum geometry for contacting a smooth glass surface is presented with discussions on the compromise between fiber tip-contact area and fiber compliance. A friction design map is developed, which shows that the theoretical optimum design condition agrees well with the LDPE nanofiber geometries exhibiting high measured friction. © 2011 American Chemical Society

Oriented nanofibers embedded in a polymer matrix

Science.gov (United States)

Barrera, Enrique V. (Inventor); Lozano, Karen (Inventor); Rodriguez-Macias, Fernando J. (Inventor); Chibante, Luis Paulo Felipe (Inventor); Stewart, David Harris (Inventor)

2011-01-01

A method of forming a composite of embedded nanofibers in a polymer matrix is disclosed. The method includes incorporating nanofibers in a plastic matrix forming agglomerates, and uniformly distributing the nanofibers by exposing the agglomerates to hydrodynamic stresses. The hydrodynamic said stresses force the agglomerates to break apart. In combination or additionally elongational flow is used to achieve small diameters and alignment. A nanofiber reinforced polymer composite system is disclosed. The system includes a plurality of nanofibers that are embedded in polymer matrices in micron size fibers. A method for producing nanotube continuous fibers is disclosed. Nanofibers are fibrils with diameters of 100 nm, multiwall nanotubes, single wall nanotubes and their various functionalized and derivatized forms. The method includes mixing a nanofiber in a polymer; and inducing an orientation of the nanofibers that enables the nanofibers to be used to enhance mechanical, thermal and electrical properties. Orientation is induced by high shear mixing and elongational flow, singly or in combination. The polymer may be removed from said nanofibers, leaving micron size fibers of aligned nanofibers.

Hyperbranched-polyol-tethered poly (amic acid) electrospun nanofiber membrane with ultrahigh adsorption capacity for boron removal

Energy Technology Data Exchange (ETDEWEB)

Wang, Zhe; Wu, Zhongyu; Zhang, Yufeng; Meng, Jianqiang, E-mail: jianqiang.meng@hotmail.com

2017-04-30

Highlights: • Electrospun nanofiber membranes were grafted with hyperbranched polyols. • The membrane had a maximum boron uptake of 5.68 mmol/g. • The membrane could adsorb 0.82 mmol/g boron from a 5 mg/L solution in 15 min. • The membrane obeyed the Langmuir and the pseudo-first-order kinetic model. • The regeneration efficiency remained over 90% after 10 cycled uses. - Abstract: The development of efficient adsorbents with high sorption capacity remains as a challenge for the removal of micropollutants occurred globally in water resources. In this work, poly (amic acid) (PAA) electrospun nanofiber membranes grafted with hyperbranched polyols were synthesized and used for boron removal. The PAA nanofiber was reacted with hyperbranched polyethylenimine (HPEI) and further with glycidol to introduce the vicinal hydroxyl groups. The chemical composition and surface characteristics of the obtained PAA-g-PG membranes were evaluated by FESEM, FTIR, XPS and water contact angles (WCA) measurements. The boron adsorption thermodynamics and kinetics were investigated systematically. The results showed that the PAA nanofiber spun from concentration of 15% had uniform morphology and narrow diameter distribution. The PAA-g-PG nanofiber membrane had a maximum boron uptake of 5.68 mmol/g and could adsorb 0.82 mmol/g boron from a 5 mg/L solution in 15 min. Both the high surface area of nanofibers and the hyperbranched structure should contribute to the high boron uptake and high adsorption rate. The nanofiber membrane obeyed the Langmuir adsorption model and the pseudo-first-order kinetic model. The regeneration efficiency of the nanofiber membrane remained 93.9% after 10 cycled uses, indicating good regenerability of the membrane.

Gas diffusion electrode based on electrospun Pani/CNF nanofibers hybrid for proton exchange membrane fuel cells (PEMFC) applications

Energy Technology Data Exchange (ETDEWEB)

Hezarjaribi, M.; Jahanshahi, M., E-mail: mjahan@nit.ac.ir; Rahimpour, A.; Yaldagard, M.

2014-03-01

A novel hybrid system has been investigated based on polyaniline/carbon nanofiber (Pani/CNF) electrospun nanofibers for modification of gas diffusion electrode (GDE) in proton exchange membrane fuel cells (PEMFC). Pani/CNF hybrid nanofibers were synthesized directly on carbon paper by electrospinning method. For preparation of catalyst ink, 20 wt.% Pt/C electrocatalyst with a platinum loading of 0.4 mg cm{sup −2} was prepared by polyol technique. SEM studies applied for morphological study of the modified GDE with hybrid nanofibers. This technique indicated that the electrospun nanofibers had a diameter of roughly 100 nm. XRD patterns also showed that the average size of Pt nanoparticles was about 2 nm. Subsequently, comparison of the hybrid electrode electrochemical behavior and 20 wt.% Pt/C commercial one was studied by cyclic voltammetry experiment. The electrochemical data indicated that the hybrid electrode exhibited higher current density (about 15 mA cm{sup −2}) and ESA (160 m{sup 2} gr{sup −1}) than commercial Pt/C with amount of about 10 mA cm{sup −2} and 114 m{sup 2} gr{sup −1}, respectively. The results herein demonstrate that Pani/CNF nanofibers can be used as a good alternative electrode material for PEMFCs.

Corrosion protection performance of waterborne epoxy coatings containing self-doped polyaniline nanofiber

Energy Technology Data Exchange (ETDEWEB)

Qiu, Shihui [Key Laboratory of Marine Materials and Related Technologies, Zhejiang Key Laboratory of Marine Materials and Protective Technologies, Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo, 315201 (China); Faculty of Materials Science and Chemical Engineering, Ningbo University, Ningbo, 315211 (China); Chen, Cheng; Cui, Mingjun [Key Laboratory of Marine Materials and Related Technologies, Zhejiang Key Laboratory of Marine Materials and Protective Technologies, Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo, 315201 (China); Li, Wei [Faculty of Materials Science and Chemical Engineering, Ningbo University, Ningbo, 315211 (China); Zhao, Haichao, E-mail: zhaohaichao@nimte.ac.cn [Key Laboratory of Marine Materials and Related Technologies, Zhejiang Key Laboratory of Marine Materials and Protective Technologies, Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo, 315201 (China); Wang, Liping, E-mail: wangliping@nimte.ac.cn [Key Laboratory of Marine Materials and Related Technologies, Zhejiang Key Laboratory of Marine Materials and Protective Technologies, Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo, 315201 (China)

2017-06-15

Highlights: • Self-dopedpolyaniline (SPANi) with good conductivity and dispersibility in water was copolymerized by aniline and its derivative. • Environmental friendly SPANi/epoxy composite coating with remarkable anti-corrosion performance was prepared. • The corrosion product of pure epoxy or composite coating was characterized by X-ray diffraction pattern and scanning electron microscope (SEM). - Abstract: Self-doped sulfonated polyaniline (SPANi) nanofiber was synthesized by the copolymerization of 2-aminobenzenesulfonic acid (ASA) and aniline via a rapid mixing polymerization approach. The chemical structure of SPANi was investigated by the Fourier-transform infrared (FT-IR), Raman, X-ray photoelectron spectroscopy (XPS), UV–vis spectra and X-ray diffraction (XRD) pattern. The as-prepared SPANi nanofibers had 45 nm average diameter and length up to 750 nm as measured by scanning electron microscope (SEM) and transmission electron microscope (TEM). The self-doped SPANi nanofiber possessed excellent aqueous solubility, good conductivity (0.11 S/cm) and reversible redox activity, making it suitable as a corrosion inhibitor for waterborne coatings. The prepared SPANi/waterborne epoxy composite coatings exhibited remarkably improved corrosion protection compared with pure waterborne epoxy coating as proved by the polarization curves and electrochemical impedance spectroscopy (EIS). The passivation effect of SPANi nanofiber and the corrosion products beneath the epoxy coatings immersed in 3.5% NaCl solution as a function of time were also investigated in this study.

Corrosion protection performance of waterborne epoxy coatings containing self-doped polyaniline nanofiber

International Nuclear Information System (INIS)

Qiu, Shihui; Chen, Cheng; Cui, Mingjun; Li, Wei; Zhao, Haichao; Wang, Liping

2017-01-01

Highlights: • Self-dopedpolyaniline (SPANi) with good conductivity and dispersibility in water was copolymerized by aniline and its derivative. • Environmental friendly SPANi/epoxy composite coating with remarkable anti-corrosion performance was prepared. • The corrosion product of pure epoxy or composite coating was characterized by X-ray diffraction pattern and scanning electron microscope (SEM). - Abstract: Self-doped sulfonated polyaniline (SPANi) nanofiber was synthesized by the copolymerization of 2-aminobenzenesulfonic acid (ASA) and aniline via a rapid mixing polymerization approach. The chemical structure of SPANi was investigated by the Fourier-transform infrared (FT-IR), Raman, X-ray photoelectron spectroscopy (XPS), UV–vis spectra and X-ray diffraction (XRD) pattern. The as-prepared SPANi nanofibers had 45 nm average diameter and length up to 750 nm as measured by scanning electron microscope (SEM) and transmission electron microscope (TEM). The self-doped SPANi nanofiber possessed excellent aqueous solubility, good conductivity (0.11 S/cm) and reversible redox activity, making it suitable as a corrosion inhibitor for waterborne coatings. The prepared SPANi/waterborne epoxy composite coatings exhibited remarkably improved corrosion protection compared with pure waterborne epoxy coating as proved by the polarization curves and electrochemical impedance spectroscopy (EIS). The passivation effect of SPANi nanofiber and the corrosion products beneath the epoxy coatings immersed in 3.5% NaCl solution as a function of time were also investigated in this study.

Aligned Layers of Silver Nano-Fibers

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Andrii B. Golovin

2012-02-01

Full Text Available We describe a new dichroic polarizers made by ordering silver nano-fibers to aligned layers. The aligned layers consist of nano-fibers and self-assembled molecular aggregates of lyotropic liquid crystals. Unidirectional alignment of the layers is achieved by means of mechanical shearing. Aligned layers of silver nano-fibers are partially transparent to a linearly polarized electromagnetic radiation. The unidirectional alignment and density of the silver nano-fibers determine degree of polarization of transmitted light. The aligned layers of silver nano-fibers might be used in optics, microwave applications, and organic electronics.

Formation of inorganic nanofibers by heat-treatment of poly(vinyl alcohol-zirconium compound hybrid nanofibers

Directory of Open Access Journals (Sweden)

Nakane K.

2013-01-01

Full Text Available Poly(vinyl alcohol-zirconium compound hybrid nanofibers (precursors were formed by electrospinning employing water as a solvent for the spinning solution. The precursors were converted into oxide (ZrO2, carbide (ZrC or nitride (ZrN nanofibers by heating them in air, Ar or N2 atmospheres. Monoclinic ZrO2 nanofibers with high-specific surface area were obtained by heat-treatment of the precursors in air. ZrC and ZrN nanofibers could be obtained below theoretical temperatures calculated from thermodynamics data.

Interrogating vertically oriented carbon nanofibers with nanomanipulation for nanoelectromechanical switching applications

International Nuclear Information System (INIS)

Kaul, Anupama B.; Megerian, Krikor G.; LeDuc, Henry G.; Epp, Larry; Khan, Abdur R.; Bagge, Leif

2009-01-01

We have demonstrated electrostatic switching in vertically oriented carbon nanofibers synthesized on refractory metallic nitride substrates, where pull-in voltages V pi ranged from 10 to 40 V. A nanoprobe was used as the actuating electrode inside a scanning-electron microscope and van der Waals interactions at these length scales appeared significant, suggesting such structures are promising for nonvolatile memory applications. A finite element model was also developed to determine a theoretical V pi and results were compared to experiment. Nanomanipulation tests also revealed tubes synthesized directly on Si by dc plasma-enhanced chemical-vapor deposition with ammonia and acetylene were electrically unsuitable for dc nanoelectromechanical switching applications.

Influence of La Doping on Magnetic and Optical Properties of Bismuth Ferrite Nanofibers

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Ziang Zhang

2012-01-01

Full Text Available The influence of La doping on the crystal structure, ferromagnetic, and optical properties of BFO nanofibers was investigated. Bi1−xLaxFeO3 ultrafine nanofibers were synthesized by the electrospinning method. The surface morphology and crystal structure of the as-spun and sintered fibers were not affected by the doping. The impurity phases of the BFO crystals were weakened with the increment of La concentration. The magnetization field curves showed that the magnetization weakened under low La doping proportion, but strengthened with the increase of the doped proportion. The magnetization curves also showed continuous strong enhancement of ferromagnetic behavior. The results of UV-vis and photoabsorption testing revealed little influence of La doping on the optical property.

Electrospun nanofiber scaffolds: engineering soft tissues

International Nuclear Information System (INIS)

Kumbar, S G; Nukavarapu, S P; Laurencin, C T; James, R

2008-01-01

Electrospinning has emerged to be a simple, elegant and scalable technique to fabricate polymeric nanofibers. Pure polymers as well as blends and composites of both natural and synthetics have been successfully electrospun into nanofiber matrices. Physiochemical properties of nanofiber matrices can be controlled by manipulating electrospinning parameters to meet the requirements of a specific application. Such efforts include the fabrication of fiber matrices containing nanofibers, microfibers, combination of nano-microfibers and also different fiber orientation/alignments. Polymeric nanofiber matrices have been extensively investigated for diversified uses such as filtration, barrier fabrics, wipes, personal care, biomedical and pharmaceutical applications. Recently electrospun nanofiber matrices have gained a lot of attention, and are being explored as scaffolds in tissue engineering due to their properties that can modulate cellular behavior. Electrospun nanofiber matrices show morphological similarities to the natural extra-cellular matrix (ECM), characterized by ultrafine continuous fibers, high surface-to-volume ratio, high porosity and variable pore-size distribution. Efforts have been made to modify nanofiber surfaces with several bioactive molecules to provide cells with the necessary chemical cues and a more in vivo like environment. The current paper provides an overlook on such efforts in designing nanofiber matrices as scaffolds in the regeneration of various soft tissues including skin, blood vessel, tendon/ligament, cardiac patch, nerve and skeletal muscle

Electrospun nanofiber scaffolds: engineering soft tissues

Energy Technology Data Exchange (ETDEWEB)

Kumbar, S G; Nukavarapu, S P; Laurencin, C T [Department of Orthopaedic Surgery, University of Virginia, VA 22908 (United States); James, R [Department of Biomedical Engineering, University of Virginia, VA 22908 (United States)], E-mail: laurencin@virginia.edu

2008-09-01

Electrospinning has emerged to be a simple, elegant and scalable technique to fabricate polymeric nanofibers. Pure polymers as well as blends and composites of both natural and synthetics have been successfully electrospun into nanofiber matrices. Physiochemical properties of nanofiber matrices can be controlled by manipulating electrospinning parameters to meet the requirements of a specific application. Such efforts include the fabrication of fiber matrices containing nanofibers, microfibers, combination of nano-microfibers and also different fiber orientation/alignments. Polymeric nanofiber matrices have been extensively investigated for diversified uses such as filtration, barrier fabrics, wipes, personal care, biomedical and pharmaceutical applications. Recently electrospun nanofiber matrices have gained a lot of attention, and are being explored as scaffolds in tissue engineering due to their properties that can modulate cellular behavior. Electrospun nanofiber matrices show morphological similarities to the natural extra-cellular matrix (ECM), characterized by ultrafine continuous fibers, high surface-to-volume ratio, high porosity and variable pore-size distribution. Efforts have been made to modify nanofiber surfaces with several bioactive molecules to provide cells with the necessary chemical cues and a more in vivo like environment. The current paper provides an overlook on such efforts in designing nanofiber matrices as scaffolds in the regeneration of various soft tissues including skin, blood vessel, tendon/ligament, cardiac patch, nerve and skeletal muscle.

Magnetic and optical properties of electrospun hollow nanofibers of SnO{sub 2} doped with Ce-ion

Energy Technology Data Exchange (ETDEWEB)

Mohanapriya, P.; Victor Jaya, N. [Department of Physics, Anna University, Chennai 600 025 (India); Pradeepkumar, R. [Centre for Nanoscience and Technology, Anna University, Chennai 600 025 (India); Natarajan, T. S., E-mail: tsn@physics.iitm.ac.in [Department of Physics, Indian Institute of Technology Madras, Chennai 600 036 (India)

2014-07-14

Cerium doped SnO{sub 2} hollow nanofibers were synthesized by electrospinning. High resolution scanning electron microscope (HRSEM) and transmission electron microscopy (TEM) analysis showed hollow nanofibers with diameters around ∼200 nm. The optimized substitution of Ce ion into SnO{sub 2} lattices happened above 6 mol. % doping as confirmed by Powder X-ray diffraction (XRD) studies. Optical band gap was decreased by the doping confirming the direct energy transfer between f-electrons of rare earth ion and the SnO{sub 2} conduction or valence band. The compound also exhibited room temperature ferromagnetism with the saturation magnetization of 19 × 10{sup −5} emu/g at 6 mol. %. This study demonstrates the Ce doped SnO{sub 2} hollow nanofibers for applications in magneto-optoelectronic devices.

Synergism of Electrospinning and Nano-alumina Trihydrate on the Polymorphism, Crystallinity and Piezoelectric Performance of PVDF Nanofibers

Science.gov (United States)

Khalifa, Mohammed; Deeksha, B.; Mahendran, Arunjunairaj; Anandhan, S.

2018-03-01

Poly(vinlylidene fluoride) (PVDF) is known for its electroactive phases, which can be nucleated by incorporating nanoparticles into PVDF to enhance its piezoelectric performance. In this study, the synergistic effect of electrospinning and nano alumina trihydrate (ATH) filler was used to enhance the electroactive β phase of PVDF. Electrospun nanofibers of PVDF/ATH nanocomposite (PANCF) were synthesized with different loadings of ATH. The presence of ATH enhances the surface charges of the electrospun droplets, leading to thinner fibers. The highest β-phase content was found to be 70.1% for PANCF with 10% ATH. The piezoelectric performance of the nanofiber mats was studied using an indigenous setup. The highest voltage output of 840 mV was produced by PANCF with 10% ATH. These nanofibers could be a promising material in the field of sensors, actuators and energy-harvesting applications.

RGO/InVO4 hollowed-out nanofibers: Electrospinning synthesis and its application in photocatalysis

International Nuclear Information System (INIS)

Ma, Dong; Zhang, Yanxiang; Gao, Mengchun; Xin, Yanjun; Wu, Juan; Bao, Nan

2015-01-01

Graphical abstract: - Highlights: • RGO/InVO 4 hollow-out nanofibers were obtained by electrospinning method. • The properties of InVO 4 hollow-out nanofibers were deeply influenced by RGO. • RGO could reduce recombination of e − –h + pairs to improve photocatalytic activity. • Photo-induced h + and e − are the two main reactive species for RhB degradation. - Abstract: A composite of reduced graphene oxide (RGO) and InVO 4 nanofiber was successfully synthesized by an electrospinning technique. The as-collected fibers were calcined at 420 °C in air and then calcined at 550 °C in nitrogen gas to remove polyvinyl pyrrolidone (PVP), which could enable InVO 4 to crystallize and protect the RGO from oxidation. The InVO 4 in the composite illustrated a hollowed-out fibrous morphology and orthorhombic phase, and RGO nanosheets were nested in the InVO 4 nanofibers. The hybrid RGO could produce more hydroxyl groups and a higher oxygen vacancy density on the surface of RGO/InVO 4 composite. Compared with pure InVO 4 , the light absorption range of the as-prepared RGO/InVO 4 composite was expanded. In Rh B degradation, the RGO/InVO 4 hybrid nanofibers displayed a higher photocatalytic activity than pure InVO 4 nanofibers. The enhanced photocatalytic activity might be ascribed to the role of RGO as an electron transporter and acceptor in the composite, which could effectively inhibit the charge recombination and facilitate the charge transfer. The exported electron could attack an O 2 molecule to facilitate the generation of • O 2 − and • OH for the photodegradation process of Rh B.

One–step preparation of CNTs/InVO_4 hollow nanofibers by electrospinning and its photocatalytic performance under visible light

International Nuclear Information System (INIS)

, Jinan 250100 (China))" data-affiliation=" (College of Environmental Science and Engineering, Shandong University, No. 27 Shanda South Road, Jinan 250100 (China))" >Zhang, Yanxiang; Ma, Dong; Wu, Juan; , Jinan 250100 (China))" data-affiliation=" (College of Environmental Science and Engineering, Shandong University, No. 27 Shanda South Road, Jinan 250100 (China))" >Zhang, Qingzhe; Xin, Yanjun; , Jinan 250100 (China))" data-affiliation=" (College of Environmental Science and Engineering, Shandong University, No. 27 Shanda South Road, Jinan 250100 (China))" >Bao, Nan

2015-01-01

Graphical abstract: - Highlights: • CNTs/InVO_4 hollow nanofibers were obtained by electrospinning method. • The properties of InVO_4 hollow nanofibers were deeply influenced by CNTs. • CNTs could reduce recombination of e"−–h"+ pairs to improve photocatalytic activity. - Abstract: A series of InVO_4 incorporated with multi-wall carbon nanotubes (CNTs) composite nanofibers were successfully synthesized by an electrospinning technique. The as-collected nanofibers were calcined at 550 °C in air to remove polyvinyl pyrrolidone (PVP), which could enable InVO_4 to crystallize. InVO_4 in the composite illustrated a hollow fibrous morphology and orthorhombic phase, and CNTs were embedded or coated on the InVO_4 hollow nanofibers. High-resolution transmission emission microscopy (HRTEM), Fourier transform infrared spectroscopy (FTIR) spectra and X-ray photoelectron spectroscopy (XPS) spectra illustrated that CNTs were existed in the composites. The optical properties measured using UV–Vis diffuse reflectance spectroscopy (DRS) confirmed that the absorbance of InVO_4 nanofibers increased in the visible light region with the incorporation of CNTs. The photocatalytic performance of the samples was investigated by the degradation rhodamine B (Rh B) under visible light irradiation. The CNTs/InVO_4 nanofibers in Rh B degradation displayed a higher photocatalytic activity than pure InVO_4 nanofibers and 10%CNTs/InVO_4 nanoparticles. The degradation showed an optimized photocatalytic oxidation for InVO_4 nanofibers incorporated with 10wt% CNTs. The enhanced photocatalytic activity might be ascribed to the role of CNTs as an electron transporter and acceptor in the composites, which could effectively inhibit the charge recombination and facilitate the charge transfer.

Biomimetic electrospun nanofibers for tissue regeneration

International Nuclear Information System (INIS)

Liao, Susan; Li Bojun; Ma Zuwei; Wei He; Chan Casey; Ramakrishna, Seeram

2006-01-01

Nanofibers exist widely in human tissue with different patterns. Electrospinning nanotechnology has recently gained a new impetus due to the introduction of the concept of biomimetic nanofibers for tissue regeneration. The advanced electrospinning technique is a promising method to fabricate a controllable continuous nanofiber scaffold similar to the natural extracellular matrix. Thus, the biomedical field has become a significant possible application field of electrospun fibers. Although electrospinning has developed rapidly over the past few years, electrospun nanofibers are still at a premature research stage. Further comprehensive and deep studies on electrospun nanofibers are essential for promoting their biomedical applications. Current electrospun fiber materials include natural polymers, synthetic polymers and inorganic substances. This review briefly describes several typically electrospun nanofiber materials or composites that have great potential for tissue regeneration, and describes their fabrication, advantages, drawbacks and future prospects. (topical review)

Electrospinning of Nanofibers for Energy Applications

Science.gov (United States)

Sun, Guiru; Sun, Liqun; Xie, Haiming; Liu, Jia

2016-01-01

With global concerns about the shortage of fossil fuels and environmental issues, the development of efficient and clean energy storage devices has been drastically accelerated. Nanofibers are used widely for energy storage devices due to their high surface areas and porosities. Electrospinning is a versatile and efficient fabrication method for nanofibers. In this review, we mainly focus on the application of electrospun nanofibers on energy storage, such as lithium batteries, fuel cells, dye-sensitized solar cells and supercapacitors. The structure and properties of nanofibers are also summarized systematically. The special morphology of nanofibers prepared by electrospinning is significant to the functional materials for energy storage. PMID:28335256

Electrospinning of Nanofibers for Energy Applications

Directory of Open Access Journals (Sweden)

Guiru Sun

2016-07-01

Full Text Available With global concerns about the shortage of fossil fuels and environmental issues, the development of efficient and clean energy storage devices has been drastically accelerated. Nanofibers are used widely for energy storage devices due to their high surface areas and porosities. Electrospinning is a versatile and efficient fabrication method for nanofibers. In this review, we mainly focus on the application of electrospun nanofibers on energy storage, such as lithium batteries, fuel cells, dye-sensitized solar cells and supercapacitors. The structure and properties of nanofibers are also summarized systematically. The special morphology of nanofibers prepared by electrospinning is significant to the functional materials for energy storage.

Synthesis of cerium and nickel doped titanium nanofibers for hydrolysis of sodium borohydride.

Science.gov (United States)

Tamboli, Ashif H; Gosavi, S W; Terashima, Chiaki; Fujishima, Akira; Pawar, Atul A; Kim, Hern

2018-07-01

A recyclable titanium nanofibers, doped with cerium and nickel doped was successfully synthesized by using sol-gel and electrospinning method for hydrogen generation from alkali free hydrolysis of NaBH 4 . The resultant nanocomposite was characterized to find out the structural and physical-chemical properties by a series of analytical techniques such as FT-IR (Fourier transform infrared spectroscopy), XRD (X-ray diffraction), SEM (scanning electron microscope), EDX (energy-dispersive X-ray spectroscopy),N 2 adsorption-desorption and BET (Brunauer-Emmett-Teller), etc. The results revealed that cerium and nickel nanoparticles were homogeneously distributed on the surface of the TiO 2 nanofibers due to having similar oxidation state and atomic radium of TiO 2 nanofibers with CeO 2 and NiO for the effective immobilization of metal ions. The NiO doped catalyst showed superior catalytic performance towards the hydrolysis reaction of NaBH 4 at room temperature. These catalysts have ability to produce 305 mL of H 2 within the time of 160 min at room temperature. Additionally, reusability test revealed that the catalyst is active even after five runs of hydrolytic reaction, implying the as-prepared NiO doped TiO 2 nanofibers could be considered as a potential candidate catalyst for portable hydrogen fuel system such as PEMFC (proton exchange membrane fuel cells). Copyright © 2018 Elsevier Ltd. All rights reserved.

Electrospun Nanofibers: New Concepts, Materials, and Applications.

Science.gov (United States)

Xue, Jiajia; Xie, Jingwei; Liu, Wenying; Xia, Younan

2017-08-15

Electrospinning is a simple and versatile technique that relies on the electrostatic repulsion between surface charges to continuously draw nanofibers from a viscoelastic fluid. It has been applied to successfully produce nanofibers, with diameters down to tens of nanometers, from a rich variety of materials, including polymers, ceramics, small molecules, and their combinations. In addition to solid nanofibers with a smooth surface, electrospinning has also been adapted to generate nanofibers with a number of secondary structures, including those characterized by a porous, hollow, or core-sheath structure. The surface and/or interior of such nanofibers can be further functionalized with molecular species or nanoparticles during or after an electrospinning process. In addition, electrospun nanofibers can be assembled into ordered arrays or hierarchical structures by manipulation of their alignment, stacking, and/or folding. All of these attributes make electrospun nanofibers well-suited for a broad spectrum of applications, including those related to air filtration, water purification, heterogeneous catalysis, environmental protection, smart textiles, surface coating, energy harvesting/conversion/storage, encapsulation of bioactive species, drug delivery, tissue engineering, and regenerative medicine. Over the past 15 years, our group has extensively explored the use of electrospun nanofibers for a range of applications. Here we mainly focus on two examples: (i) use of ceramic nanofibers as catalytic supports for noble-metal nanoparticles and (ii) exploration of polymeric nanofibers as scaffolding materials for tissue regeneration. Because of their high porosity, high surface area to volume ratio, well-controlled composition, and good thermal stability, nonwoven membranes made of ceramic nanofibers are terrific supports for catalysts based on noble-metal nanoparticles. We have investigated the use of ceramic nanofibers made of various oxides, including SiO 2 , TiO 2

High-density platinum nanoparticle-decorated titanium dioxide nanofiber networks for efficient capillary photocatalytic hydrogen generation

Science.gov (United States)

Zhaodong Li; Chunhua Yao; Yi-Cheng Wang; Solomon Mikael; Sundaram Gunasekaran; Zhenqiang Ma; Zhiyong Cai; Xudong Wang

2016-01-01

Aldehyde-functionalized cellulose nanofibers (CNFs) were applied to synthesize Pt nanoparticles (NPs) on CNF surfaces via on-site Pt ion reduction and achieve high concentration and uniform Pt NP loading. ALD could then selectively deposit TiO2 on CNFs and keep the Pt NPs uncovered due to their drastically different hydro-affinity properties. The...

The Synthesis of Peculiar Structure of Springlike Multiwall Carbon Nanofibers/Nanotubes via Mechanothermal Method

Directory of Open Access Journals (Sweden)

Sahebali Manafi

2012-01-01

Full Text Available Mechanothermal (MT method is one of the methods used for large-scale production of carbon nanotubes/nanofibers. The different peculiar morphologies of carbon allotropes are introduced with an extraordinary structure for the first time by MT method. In this paper, the influence of milling time and annealing temperature on the crystallinity and morphology of the synthesized nanopowders was investigated. Surprisingly, in this investigation, we report the synthesis of springlike multiwalled carbon nanofibers (S-MWCNFs by a two-step annealing of milled graphite in an Ar atmosphere. On the other hand, the MT method could be used for the preparation of suitable structures with applications in nanocomposite materials, which is an important task in the era of nanotechnology.

Influence of Fabricating Process on Gas Sensing Properties of ZnO Nanofiber-Based Sensors

International Nuclear Information System (INIS)

Xu Lei; Wang Rui; Liu Yong; Dong Liang

2011-01-01

ZnO nanofibers are synthesized by an electrospinning method and characterized by x-ray diffraction (XRD) and scanning electron microscopy (SEM). Two types of gas sensors are fabricated by loading these nanofibers as the sensing materials and their performances are investigated in detail. Compared with the sensors based on traditional ceramic tubes with Au electrodes (traditional sensors), the sensors fabricated by spinning ZnO nanofibers on ceramic planes with Ag-Pd electrodes (plane sensors) exhibit much higher sensing properties. The sensitivity for the plane sensors is about 30 to 100 ppm ethanol at 300°C, while the value is only 13 for the traditional sensors. The response and recovery times are about 2 and 3s for the plane sensors and are 3 and 6s for the traditional sensors, respectively. Lower minimum-detection-limit is also found for the plane sensors. These improvements are explained by considering the morphological damage in the fabricating process for traditional sensors. The results suggest that the plane sensors are more suitable to sensing investigation for higher veracity. (general)

Properties of Electrospun Nanofibers of Multi-Block Copolymers of [Poly-ε-caprolactone-b-poly(tetrahydrofuran-co-ε-caprolactone]m Synthesized by Janus Polymerization

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Muhammad Ijaz Shah

2017-10-01

Full Text Available Novel biodegradable multiblock copolymers of [PCL-b-P(THF-co-CL]m with PCL fractions of 53.3 and 88.4 wt % were prepared by Janus polymerization of ε-caprolactone (CL and tetrahydrofuran (THF. Their electrospun mats were obtained with optimized parameters containing bead-free nanofibers whose diameters were between 290 and 520 nm. The mechanical properties of the nanofiber scaffolds were measured showing the tensile strength and strain at break of 8–10 MPa and 123–161%, respectively. Annealing improved their mechanical properties and their tensile strength and strain at break of the samples increased to 10–13 MPa and 267–338%, respectively. Due to the porous structure and crystallization in nanoscale confinement, the mechanical properties of the nanofiber scaffolds appeared as plastics, rather than as the elastomers observed in bulk thermal-molded film.

Preparation of Pr-doped SnO{sub 2} hollow nanofibers by electrospinning method and their gas sensing properties

Energy Technology Data Exchange (ETDEWEB)

Li, W.Q.; Ma, S.Y., E-mail: lwq19891013@126.com; Li, Y.F.; Li, X.B.; Wang, C.Y.; Yang, X.H.; Cheng, L.; Mao, Y.Z.; Luo, J.; Gengzang, D.J.; Wan, G.X.; Xu, X.L.

2014-08-25

Highlights: • Pr-doped SnO{sub 2} hollow nanofibers were fabricated by electrospinning. • The crystal structures, surface morphology, chemical state and gas sensing performance were investigated. • The Pr-doped SnO{sub 2} hollow structure exhibited good gas-sensing properties to ethanol at 300 °C. • The relationships between response time (recovery time) and temperature, response time (recovery time) and concentration were investigated. • A sensor mechanism of hollow nanofibers depend on temperature was discussed. - Abstract: Pure and Pr-doped SnO{sub 2} hollow nanofibers were fabricated through a facile single capillary electrospinning and followed by calcination. The properties of as-synthesized nanofibers were characterized by scanning electron microscopy, Brunauer–Emmett–Teller, transmission electron microscopy, X-ray diffraction and X-ray photoelectron spectroscopy. Compared with pure fibers, Pr-doped SnO{sub 2} nanofibers exhibited excellent ethanol sensing properties at the optimum temperature of 300 °C. Maximum sensing response to ethanol was received in the fibers with 0.6 wt% Pr. The relationships between response time (recovery time) and temperature, response time (recovery time) and concentration were investigated. The results demonstrated that the high response and relatively short response/recovery time were related to surface area, adsorbed oxygen species and oxygen vacancies.

Design of Polymeric Nanofiber Gauze Mask to Prevent Inhaling PM2.5 Particles from Haze Pollution

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Xingzhou Li

2015-01-01

Full Text Available Recently, PM2.5 (particulate matter with diameter of 2.5 micron or less has become a major health hazard from the polluted air in many cities in China. The regular gauze masks are used to prevent inhaling the PM2.5 fine particles; however, those masks are not able to filter out the PM2.5 because of the large porosity of the mask materials. Some well-prevented masks usually have poor breathability, which increases other health risks. In this study, a polysulfone based nanofiber for mask filtration material was synthesized by electrospinning. That nanofiber mask material was characterized by SEM, air permeability test, and PM2.5 trapping experiment. The results indicate that nanofiber mask material can efficiently filter out the PM2.5 particles and simultaneously preserve a good breathability. We attribute such improvement to the nanoscaled fibers, having the same porosity as that of regular gauze mask but with extremely reduced local interfiber space.

Biofunctionalized Nanofibers Using Arthrospira (Spirulina Biomass and Biopolymer

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Michele Greque de Morais

2015-01-01

Full Text Available Electrospun nanofibers composed of polymers have been extensively researched because of their scientific and technical applications. Commercially available polyhydroxybutyrate (PHB and polyhydroxybutyrate-co-valerate (PHB-HV copolymers are good choices for such nanofibers. We used a highly integrated method, by adjusting the properties of the spinning solutions, where the cyanophyte Arthrospira (formally Spirulina was the single source for nanofiber biofunctionalization. We investigated nanofibers using PHB extracted from Spirulina and the bacteria Cupriavidus necator and compared the nanofibers to those made from commercially available PHB and PHB-HV. Our study assessed nanofiber formation and their selected thermal, mechanical, and optical properties. We found that nanofibers produced from Spirulina PHB and biofunctionalized with Spirulina biomass exhibited properties which were equal to or better than nanofibers made with commercially available PHB or PHB-HV. Our methodology is highly promising for nanofiber production and biofunctionalization and can be used in many industrial and life science applications.

Production of silk sericin/silk fibroin blend nanofibers

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Zhang Xianhua

2011-01-01

Full Text Available Abstract Silk sericin (SS/silk fibroin (SF blend nanofibers have been produced by electrospinning in a binary SS/SF trifluoroacetic acid (TFA solution system, which was prepared by mixing 20 wt.% SS TFA solution and 10 wt.% SF TFA solution to give different compositions. The diameters of the SS/SF nanofibers ranged from 33 to 837 nm, and they showed a round cross section. The surface of the SS/SF nanofibers was smooth, and the fibers possessed a bead-free structure. The average diameters of the SS/SF (75/25, 50/50, and 25/75 blend nanofibers were much thicker than that of SS and SF nanofibers. The SS/SF (100/0, 75/25, and 50/50 blend nanofibers were easily dissolved in water, while the SS/SF (25/75 and 0/100 blend nanofibers could not be completely dissolved in water. The SS/SF blend nanofibers could not be completely dissolved in methanol. The SS/SF blend nanofibers were characterized by Fourier transform infrared (FTIR spectroscopy, differential scanning calorimetry, and differential thermal analysis. FTIR showed that the SS/SF blend nanofibers possessed a random coil conformation and ß-sheet structure.

Nano-Fiber Reinforced Enhancements in Composite Polymer Matrices

Science.gov (United States)

Chamis, Christos C.

2009-01-01

Nano-fibers are used to reinforce polymer matrices to enhance the matrix dependent properties that are subsequently used in conventional structural composites. A quasi isotropic configuration is used in arranging like nano-fibers through the thickness to ascertain equiaxial enhanced matrix behavior. The nano-fiber volume ratios are used to obtain the enhanced matrix strength properties for 0.01,0.03, and 0.05 nano-fiber volume rates. These enhanced nano-fiber matrices are used with conventional fiber volume ratios of 0.3 and 0.5 to obtain the composite properties. Results show that nano-fiber enhanced matrices of higher than 0.3 nano-fiber volume ratio are degrading the composite properties.

Efficiency enhancement of ZnO-based dye-sensitized solar cell by hollow TiO{sub 2} nanofibers

Energy Technology Data Exchange (ETDEWEB)

Li, Fengrong; Wang, Guangchao; Jiao, Yu [Faculty of Materials, Optoelectronics and Physics, Key Laboratory of Low Dimensional Materials and Application Technology of Ministry of Education, Xiangtan University, Xiangtan 411105, Hunan (China); Li, Jiangyu [Department of Mechanical Engineering, University of Washington, Seattle, WA 98195-2600 (United States); Xie, Shuhong, E-mail: shxie@xtu.edu.cn [Faculty of Materials, Optoelectronics and Physics, Key Laboratory of Low Dimensional Materials and Application Technology of Ministry of Education, Xiangtan University, Xiangtan 411105, Hunan (China)

2014-10-25

Highlights: • The hollow TiO{sub 2} nanofibers were synthesized by one step electrospinning method. • We studied the performance of DSSC with different TiO{sub 2} weight ratioes. • The hollow TiO{sub 2} nanofibers enhance light scattering and suppress electrons recombination. • The efficiency of DSSC improved from 2.82% to 4.59% by adding 10 wt.% of TiO{sub 2}. - Abstract: One-dimensional nanostructures as the photoanode of dye-sensitized solar cell (DSSC) can provide a direct transport pathway for electrons injection to increase electrons transfer efficiency. In this work, hollow TiO{sub 2} nanofibers were fabricated by one step electrospinning based on sol–gel method, and were used to successfully enhance the conversion efficiency of ZnO-based DSSC. The effects of different TiO{sub 2} weight percentages on the performance of TiO{sub 2}/ZnO composite photoanode were investigated systematically. The results indicate that the light scattering of the photoanode film is increased and the electrons recombination is suppressed when appropriate amount of hollow TiO{sub 2} nanofibers was added into ZnO. The maximal energy conversion efficiency reaches 4.59% by adding 10 wt.% of hollow TiO{sub 2} nanofibers, which is 62% higher than that of DSSC based on pure ZnO nanoparticles.

Polyhydroxybutyrate and phenolic compounds microalgae electrospun nanofibers: A novel nanomaterial with antibacterial activity.

Science.gov (United States)

Kuntzler, Suelen Goettems; Almeida, Ana Claudia Araujo de; Costa, Jorge Alberto Vieira; Morais, Michele Greque de

2018-07-01

Polymer nanofibers produced by electrospinning are promising for use in food packaging because of their nanometric diameter, which provides a barrier to external conditions above the possible incorporation of the active compounds. The microalga Spirulina sp. LEB 18 synthesizes bioproducts, such as polyhydroxybutyrate (PHB), which is biodegradable and has similar mechanical and thermal properties to polymers of petrochemical origin. Moreover, phenolic compounds of microalgae have antibacterial, antifungal, and antioxidant activities, which is a differential for the development of packaging. The objective of the study was to develop a nanomaterial with antibacterial action from bioproducts of microalgal origin. PHB nanofibers containing phenolic compounds presented average diameter of 810±85nm exhibited hydrophobicity, which gave protection to the food relative to the moisture outside the package. These nanofibers showed inhibition of the growth of Staphylococcus aureus ATCC 25923 with a zone of 7.5±0.4mm. Thermal and mechanical properties have confirmed the potential applicability of this material as food packaging. This new nanomaterial combines a packaging function to protect products and to be biodegradable with the antibacterial activity that prevents the proliferation of microorganisms and ensures the quality and preservation of food. Published by Elsevier B.V.

Evaluation of the genotoxicity of cellulose nanofibers.

Science.gov (United States)

de Lima, Renata; Oliveira Feitosa, Leandro; Rodrigues Maruyama, Cintia; Abreu Barga, Mariana; Yamawaki, Patrícia Cristina; Vieira, Isolda Jesus; Teixeira, Eliangela M; Corrêa, Ana Carolina; Caparelli Mattoso, Luiz Henrique; Fernandes Fraceto, Leonardo

2012-01-01

Agricultural products and by products provide the primary materials for a variety of technological applications in diverse industrial sectors. Agro-industrial wastes, such as cotton and curaua fibers, are used to prepare nanofibers for use in thermoplastic films, where they are combined with polymeric matrices, and in biomedical applications such as tissue engineering, amongst other applications. The development of products containing nanofibers offers a promising alternative for the use of agricultural products, adding value to the chains of production. However, the emergence of new nanotechnological products demands that their risks to human health and the environment be evaluated. This has resulted in the creation of the new area of nanotoxicology, which addresses the toxicological aspects of these materials. Contributing to these developments, the present work involved a genotoxicological study of different nanofibers, employing chromosomal aberration and comet assays, as well as cytogenetic and molecular analyses, to obtain preliminary information concerning nanofiber safety. The methodology consisted of exposure of Allium cepa roots, and animal cell cultures (lymphocytes and fibroblasts), to different types of nanofibers. Negative controls, without nanofibers present in the medium, were used for comparison. The nanofibers induced different responses according to the cell type used. In plant cells, the most genotoxic nanofibers were those derived from green, white, and brown cotton, and curaua, while genotoxicity in animal cells was observed using nanofibers from brown cotton and curaua. An important finding was that ruby cotton nanofibers did not cause any significant DNA breaks in the cell types employed. This work demonstrates the feasibility of determining the genotoxic potential of nanofibers derived from plant cellulose to obtain information vital both for the future usage of these materials in agribusiness and for an understanding of their environmental

Chlorine effect on the formation of carbon nanofibers.

Science.gov (United States)

Lin, Wang-Hua; Takahashi, Yusuke; Li, Yuan-Yao; Sakoda, Akiyoshi

2012-12-01

Platelet graphite nanofibers (GNFs) and turbostratic carbon nanofibers (CNFs) are synthesized by the thermal evaporation and decomposition of a polymer-based mixture at 700 degrees C using Ni as a catalyst. The mixture consists of poly(ethylene glycol) (PEG), serving as the carbon source, and hydrochloric acid solution (HCl(aq)), serving as the promoter/additive for the growth of CNFs. High-purity zigzag-shaped platelet GNFs form with 10 wt% HCl(aq) as an additive in the PEG. The diameters of the platelet GNFs are in the range of 40-60 nm, with lengths of a few micrometers. High-resolution transmission electron microscopy images indicate a high degree of graphitization and well ordered graphene layers along the fiber axis. In contrast, high-purity turbostratic CNFs form with 20 wt% HCl(aq) in the PEG. The diameter and length of the turbostratic CNFs are 20-40 nm and a few micrometers, respectively. The participation of HCl in the thermal process leads to the formation of Ni-Cl compounds. The amount of chlorine affects the shape of the Ni catalyst, which determines the type of CNF formed.

Synthesis and electrochemical performance of mesoporous SiO{sub 2}–carbon nanofibers composite as anode materials for lithium secondary batteries

Energy Technology Data Exchange (ETDEWEB)

Hyun, Yura; Choi, Jin-Yeong [Department of Chemistry, Keimyung University (Korea, Republic of); Park, Heai-Ku [Department of Chemical Engineering, Keimyung University (Korea, Republic of); Bae, Jae Young [Department of Chemistry, Keimyung University (Korea, Republic of); Lee, Chang-Seop, E-mail: surfkm@kmu.ac.kr [Department of Chemistry, Keimyung University (Korea, Republic of)

2016-10-15

Highlights: • Mesoporous SiO{sub 2}–carbon nanofibers composite synthesized on Ni foam without any binder. • This composite was directly applied as anode material of Li secondary batteries. • Showed the highest initial (2420 mAh/g) and discharging (2092 mAh/g) capacity. • This material achieved a retention rate of 86.4% after 30 cycles. - Abstract: In this study, carbon nanofibers (CNFs) and mesoporous SiO{sub 2}–carbon nanofibers composite were synthesized and applied as the anode materials in lithium secondary batteries. CNFs and mesoporous SiO{sub 2}–CNFs composite were grown via chemical vapor deposition method with iron-copper catalysts. Mesoporous SiO{sub 2} materials were prepared by sol–gel method using tetraethylorthosilicate as the silica source and cetyltrimethylammoniumchloride as the template. Ethylene was used as the carbon source and passes into a quartz reactor of a tube furnace heated to 600 °C, and the temperature was maintained at 600 °C for 10 min to synthesize CNFs and mesoporous SiO{sub 2}–CNFs composite. The electrochemical characteristics of the as-prepared CNFs and mesoporous SiO{sub 2}–CNFs composite as the anode of lithium secondary batteries were investigated using a three-electrode cell. In particular, the mesoporous SiO{sub 2}–CNFs composites synthesized without binder after depositing mesoporous SiO{sub 2} on Ni foam showed the highest charging and discharging capacity and retention rate. The initial capacity (2420 mAh/g) of mesoporous SiO{sub 2}–CNFs composites decreased to 2092 mAh/g after 30 cycles at a retention rate of 86.4%.

A novel electrospun silk fibroin/hydroxyapatite hybrid nanofibers

International Nuclear Information System (INIS)

Ming, Jinfa; Zuo, Baoqi

2012-01-01

A novel electrospinning of silk fibroin/hydroxyapatite hybrid nanofibers with different composition ratios was performed with methanoic acid as a spinning solvent. The silk fibroin/hydroxyapatite hybrids containing up to 30% hydroxyapatite nanoparticles could be electrospun into the continuous fibrous structure. The electrospun silk fibroin/hydroxyapatite hybrid nanofibers showed bigger diameter and wider diameter distribution than pure silk fibroin nanofibers, and the average diameter gradually increased from 95 to 582 nm. At the same time, the secondary structure of silk fibroin/hydroxyapatite nanofibers was characterized by X-ray diffraction, Fourier transform infrared analysis, and DSC measurement. Comparing with the pure silk fibroin nanofibers, the crystal structure of silk fibroin was mainly amorphous structure in the hybrid nanofibers. X-ray diffraction results demonstrated the hydroxyapatite crystalline nature remained as evidenced from the diffraction planes (002), (211), (300), and (202) of the hydroxyapatite crystallites, which was also confirmed by Fourier transform infrared analysis. The thermal behavior of hybrid nanofibers exhibited the endothermic peak of moisture evaporation ranging from 86 to 113 °C, and the degradation peak at 286 °C appeared. The SF/HAp nanofibers mats containing 30% HAp nanoparticles showed higher breaking tenacity and extension at break for 1.1688 ± 0.0398 MPa and 6.55 ± 1.95%, respectively. Therefore, the electrospun silk fibroin/hydroxyapatite hybrid nanofibers should be provided potentially useful options for the fabrication of biomaterial scaffolds for bone tissue engineering. -- Highlights: ► The novel SF/HAp nanofibers were directly prepared by electrospinning method. ► The nanofiber diameter had significant related to the content of HAp. ► The crystal structure of silk fibroin was mainly amorphous structure in the hybrid nanofibers. ► The HAp crystals existing in the hybrid nanofibers were characterized

Graphene-doped carbon/Fe3O4 porous nanofibers with hierarchical band construction as high-performance anodes for lithium-ion batteries

International Nuclear Information System (INIS)

He, Jianxin; Zhao, Shuyuan; Lian, Yanping; Zhou, Mengjuan; Wang, Lidan; Ding, Bin; Cui, Shizhong

2017-01-01

Highlights: • GN@C/Fe 3 O 4 are synthesized via in-situ electrospinning and thermal treatment. • GN@C/Fe 3 O 4 show unique dark/light banding with a hierarchical porous structure. • Doped graphene induces a uniform distribution of smaller size Fe 3 O 4 nanoparticles. • Doped graphene provides more active sites and accommodate the volume change. • GN@C/Fe 3 O 4 electrode displays a reversible capacity of 872 mAh/g after 100 cycles. - Abstract: Porous graphene-doped carbon/Fe 3 O 4 (GN@C/Fe 3 O 4 ) nanofibers are synthesized via in-situ electrospinning and subsequent thermal treatment for use as lithium-ion battery anode materials. A polyacrylonitrile (PAN)/polymethyl methacrylate (PMMA) solution containing ferric acetylacetone and graphene oxide nanosheets is used as the electrospinning precursor solution. The resulting porous GN@C/Fe 3 O 4 nanofibers show unique dark/light banding and a hierarchical porous structure. These nanofibers have a Brunauer–Emmett–Teller (BET) specific surface area of 323.0 m 2 /g with a total pore volume of 0.337 cm 3 /g, which is significantly greater than that of a sample without graphene and C/Fe 3 O 4 nanofibers. The GN@C/Fe 3 O 4 nanofiber electrode displays a reversible capacity of 872 mAh/g at a current density of 100 mA/g after 100 cycles, excellent cycling stability, and superior rate capability (455 mA/g at 5 A/g). The excellent performance of porous GN@C/Fe 3 O 4 is attributed to the material’s unique structure, including its striped topography, hierarchical porous structure, and inlaid flexible graphene, which not only provides more accessible active sites for lithium-ion insertion and high-efficiency transport pathways for ions and electrons, but also accommodates the volume change associated with lithium insertion/extraction. Moreover, the zero-valent iron and graphene in the porous nanofibers enhance the conductivity of the electrodes.

A simple approach for synthesis, characterization and bioactivity of bovine bones to fabricate the polyurethane nanofiber containing hydroxyapatite nanoparticles

DEFF Research Database (Denmark)

Sheikh, F. A.; Kanjwal, Muzafar Ahmed; Macossay, J.

2012-01-01

In the present study, we had introduced polyurethane (PU) nanofibers that contain hydroxyapatite (HAp) nanoparticles (NPs) as a result of an electrospinning process. A simple method that does not depend on additional foreign chemicals had been employed to synthesize HAp NPs through the calcination...

Synthesis of a novel carbon nanofiber structure for removal of lead

International Nuclear Information System (INIS)

Faghihian, Hossein; Kooravand, Masoume; Atarodi, Homa

2013-01-01

A new structure of carbon nanofibers was synthesized by chemical vapor deposition method. Kaolin was used as substrate and cyclohexanol and ferrocene as carbon source and catalyst, respectively. The morphology of the product was studied by scanning electron microscopy. Carbon nanofiber was modified with a mixture of nitric acid and sulfuric acid to enhance its adsorption capacity. The presence of functional groups on the treated adsorbent was assessed by FT-IR spectroscopy. The surface activity of the oxidized sample was estimated by Boehm’s titration. The pH_(_P_Z_C_) of the samples was also measured. The adsorbent was then used for adsorption of Pb"2"+ at different experimental conditions. The optimized capacity of 211mg·g"−"1 was obtained. Kinetic and thermodynamic of the reaction were studied. It was concluded that the adsorption process is spontaneous and endothermic. Equilibrium data were well fitted to the Langmuir model and the pseudo-second-order kinetic model described the adsorption process

Synergetic interface between NiO/Ni3S2 nanosheets and carbon nanofiber as binder-free anode for highly reversible lithium storage

Science.gov (United States)

Jiang, Jialin; Ma, Chao; Yang, Yinbo; Ding, Jingjing; Ji, Hongmei; Shi, Shaojun; Yang, Gang

2018-05-01

A novel heterostructure of NiO/Ni3S2 nanoflake is synthesized and composited with carbon nanofibers (CNF) membrane. NiO/Ni3S2 nanoflakes are homogeneously dispersed in CNF network, herein, NiO/Ni3S2 like leaf and CNF like branch. Carbon nanofibers network efficiently prevents the pulverization and buffers the volume changes of NiO/Ni3S2, meanwhile, NiO/Ni3S2 nanoflakes through the conductive channels of carbon nanofibers own improved Li+ diffusion ability and structural stability. The capacity of NiO/Ni3S2/CNF reaches to 519.2 mA g-1 after 200 cycles at the current density of 0.5 A g-1 while NiO/Ni3S2 fades to 71 mAh g-1 after 40 cycles. Owing to the synergetic structure, the resultant binder-free electrode NiO/Ni3S2/carbon nanofibers shows an excellent reversible lithium storage capability.

Gas Sensing Properties of Indium Tin Oxide Nanofibers

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Shiyou Xu

2009-11-01

Full Text Available Indium Tin Oxide (ITO nanofibers were fabricated by the electrospinning process. The morphology and crystal structure of ITO nanofibers were studied by SEM, XRD, and TEM respectively. The results showed that polycrystalline ITO nanofibers with an average diameter of 80 nm were obtained. Sensors based on these nanofibers were fabricated by collecting these nanofibers on the integrated sensor platforms. The ITO nanofiber-based sensors showed very fast and high sensor responses at both room and elevated temperatures for NO2. The ratios of resistance in NO2 over that in air were 5 at room temperature and 34 at the optimal working temperature, respectively. The ITO nanofiber-based sensor can be repeatedly used. The details for the fast, enhanced sensor responses and the optimal temperature were discussed.

Oxidation of CO and Methanol on Pd-Ni Catalysts Supported on Different Chemically-Treated Carbon Nanofibers

Directory of Open Access Journals (Sweden)

Juan Carlos Calderón

2016-10-01

Full Text Available In this work, palladium-nickel nanoparticles supported on carbon nanofibers were synthesized, with metal contents close to 25 wt % and Pd:Ni atomic ratios near to 1:2. These catalysts were previously studied in order to determine their activity toward the oxygen reduction reaction. Before the deposition of metals, the carbon nanofibers were chemically treated in order to generate oxygen and nitrogen groups on their surface. Transmission electron microscopy analysis (TEM images revealed particle diameters between 3 and 4 nm, overcoming the sizes observed for the nanoparticles supported on carbon black (catalyst Pd-Ni CB 1:2. From the CO oxidation at different temperatures, the activation energy Eact for this reaction was determined. These values indicated a high tolerance of the catalysts toward the CO poisoning, especially in the case of the catalysts supported on the non-chemically treated carbon nanofibers. On the other hand, apparent activation energy Eap for the methanol oxidation was also determined finding—as a rate determining step—the COads diffusion to the OHads for the catalysts supported on carbon nanofibers. The results here presented showed that the surface functional groups only play a role in the obtaining of lower particle sizes, which is an important factor in the obtaining of low CO oxidation activation energies.

Photosensitive semiconducting polymer-incorporated nanofibers for promoting the regeneration of skin wound

Energy Technology Data Exchange (ETDEWEB)

Jin, Guorui [Institute of Materials Research and Engineering, A*STAR, 2 Fusionopolis Way, Innovis, #08-03, 138634 (Singapore); The Key Laboratory of Biomedical Information Engineering of Ministry of Education, Xi' an Jiaotong University, School of Life Science and Technology, Xi' an 710049 (China); Li, Jun [Institute of Materials Research and Engineering, A*STAR, 2 Fusionopolis Way, Innovis, #08-03, 138634 (Singapore); Department of Chemistry and Centre for Plastic Electronics, Imperial College London, London SW7 2AZ (United Kingdom); Li, Kai, E-mail: kai_li_cn@hotmail.com [Institute of Materials Research and Engineering, A*STAR, 2 Fusionopolis Way, Innovis, #08-03, 138634 (Singapore); Department of Radiology and Molecular Imaging Program at Stanford (MIPS), Stanford School of Medicine, Stanford, 94305 (United States)

2017-01-01

Photosensitive semiconducting polymer (SP) combined with light stimulation has shown the capability in promoting the proliferation of human dermal fibroblasts (HDFs). However, the high cytotoxicity of the used SP hindered its further application in bioactive scaffolds. In this contribution, we designed and synthesized a SP, poly (N,N-bis(2-octyldodecyl)-3,6-di(thiophen-2-yl)-2,5-dihydropyrrolo[3,4-c] pyrrole-1,4-dione-alt-thieno[3,2-b]thiophene) (PDBTT) with low cytotoxicity and strong absorbance in red and near-infrared region (600–1200 nm). The photosensitive SP was then applied in electrospun poly(ε-caprolactone) (PCL) nanofibrous scaffold and evaluated its proliferative effect on HDFs under the illumination from red light-emitting diode (LED) with high tissue penetration. After 9 days of continuous stimulation, the hybrid electrospun PCL/PDBTT nanofibers with low cytotoxicity showed excellent support for HDFs adhesion, proliferation and collagen secretion than neat PCL nanofibers and HDFs on the stimulated PCL/PDBTT nanofibers gained typical spindle morphology, indicating the well cell spreading on the stimulated PCL/PDBTT nanofibers. The incorporation of functional materials within synthetic biomaterials could be a novel way in improving the performance of engineered tissue constructs by providing multiple cues (e.g. electrical stimulation) to the attached cells. - Highlights: • A photosensitive semiconducting polymer (SP) was applied in electrospun nanofibrous scaffold. • The SP-incorporated scaffold could promote cell proliferation upon light stimulation. • The designed photosensitive SP could be applied as functional material with low cost and high durability in skin tissue engineering.

RGO/InVO{sub 4} hollowed-out nanofibers: Electrospinning synthesis and its application in photocatalysis

Energy Technology Data Exchange (ETDEWEB)

Ma, Dong [Key Lab of Marine Environment and Ecology, Ministry of Education, Ocean University of China, Qingdao 266100 (China); College of Resource and Environment, Qingdao Agricultural University, Qingdao 266109 (China); Zhang, Yanxiang [College of Environmental Science and Engineering, Shandong University, Jinan 250100 (China); Gao, Mengchun, E-mail: mengchungao@outlook.com [Key Lab of Marine Environment and Ecology, Ministry of Education, Ocean University of China, Qingdao 266100 (China); Xin, Yanjun; Wu, Juan [College of Resource and Environment, Qingdao Agricultural University, Qingdao 266109 (China); Bao, Nan [College of Environmental Science and Engineering, Shandong University, Jinan 250100 (China)

2015-10-30

Graphical abstract: - Highlights: • RGO/InVO{sub 4} hollow-out nanofibers were obtained by electrospinning method. • The properties of InVO{sub 4} hollow-out nanofibers were deeply influenced by RGO. • RGO could reduce recombination of e{sup −}–h{sup +} pairs to improve photocatalytic activity. • Photo-induced h{sup +} and e{sup −} are the two main reactive species for RhB degradation. - Abstract: A composite of reduced graphene oxide (RGO) and InVO{sub 4} nanofiber was successfully synthesized by an electrospinning technique. The as-collected fibers were calcined at 420 °C in air and then calcined at 550 °C in nitrogen gas to remove polyvinyl pyrrolidone (PVP), which could enable InVO{sub 4} to crystallize and protect the RGO from oxidation. The InVO{sub 4} in the composite illustrated a hollowed-out fibrous morphology and orthorhombic phase, and RGO nanosheets were nested in the InVO{sub 4} nanofibers. The hybrid RGO could produce more hydroxyl groups and a higher oxygen vacancy density on the surface of RGO/InVO{sub 4} composite. Compared with pure InVO{sub 4}, the light absorption range of the as-prepared RGO/InVO{sub 4} composite was expanded. In Rh B degradation, the RGO/InVO{sub 4} hybrid nanofibers displayed a higher photocatalytic activity than pure InVO{sub 4} nanofibers. The enhanced photocatalytic activity might be ascribed to the role of RGO as an electron transporter and acceptor in the composite, which could effectively inhibit the charge recombination and facilitate the charge transfer. The exported electron could attack an O{sub 2} molecule to facilitate the generation of • O{sub 2}{sup −} and • OH for the photodegradation process of Rh B.

Thermal conductivity model for nanofiber networks

Science.gov (United States)

Zhao, Xinpeng; Huang, Congliang; Liu, Qingkun; Smalyukh, Ivan I.; Yang, Ronggui

2018-02-01

Understanding thermal transport in nanofiber networks is essential for their applications in thermal management, which are used extensively as mechanically sturdy thermal insulation or high thermal conductivity materials. In this study, using the statistical theory and Fourier's law of heat conduction while accounting for both the inter-fiber contact thermal resistance and the intrinsic thermal resistance of nanofibers, an analytical model is developed to predict the thermal conductivity of nanofiber networks as a function of their geometric and thermal properties. A scaling relation between the thermal conductivity and the geometric properties including volume fraction and nanofiber length of the network is revealed. This model agrees well with both numerical simulations and experimental measurements found in the literature. This model may prove useful in analyzing the experimental results and designing nanofiber networks for both high and low thermal conductivity applications.

Thermal conductivity model for nanofiber networks

Energy Technology Data Exchange (ETDEWEB)

Zhao, Xinpeng [Department of Mechanical Engineering, University of Colorado, Boulder, Colorado 80309, USA; Huang, Congliang [Department of Mechanical Engineering, University of Colorado, Boulder, Colorado 80309, USA; School of Electrical and Power Engineering, China University of Mining and Technology, Xuzhou 221116, China; Liu, Qingkun [Department of Physics, University of Colorado, Boulder, Colorado 80309, USA; Smalyukh, Ivan I. [Department of Physics, University of Colorado, Boulder, Colorado 80309, USA; Materials Science and Engineering Program, University of Colorado, Boulder, Colorado 80309, USA; Yang, Ronggui [Department of Mechanical Engineering, University of Colorado, Boulder, Colorado 80309, USA; Materials Science and Engineering Program, University of Colorado, Boulder, Colorado 80309, USA; Buildings and Thermal Systems Center, National Renewable Energy Laboratory, Golden, Colorado 80401, USA

2018-02-28

Understanding thermal transport in nanofiber networks is essential for their applications in thermal management, which are used extensively as mechanically sturdy thermal insulation or high thermal conductivity materials. In this study, using the statistical theory and Fourier's law of heat conduction while accounting for both the inter-fiber contact thermal resistance and the intrinsic thermal resistance of nanofibers, an analytical model is developed to predict the thermal conductivity of nanofiber networks as a function of their geometric and thermal properties. A scaling relation between the thermal conductivity and the geometric properties including volume fraction and nanofiber length of the network is revealed. This model agrees well with both numerical simulations and experimental measurements found in the literature. This model may prove useful in analyzing the experimental results and designing nanofiber networks for both high and low thermal conductivity applications.

Fabrication and In Vitro/In Vivo Performance of Mucoadhesive Electrospun Nanofiber Mats Containing α-Mangostin.

Science.gov (United States)

Samprasit, Wipada; Rojanarata, Theerasak; Akkaramongkolporn, Prasert; Ngawhirunpat, Tanasait; Kaomongkolgit, Ruchadaporn; Opanasopit, Praneet

2015-10-01

This study aimed to fabricate mucoadhesive electrospun nanofiber mats containing α-mangostin for the maintenance of oral hygiene and reduction of the bacterial growth that causes dental caries. Synthesized thiolated chitosan (CS-SH) blended with polyvinyl alcohol (PVA) was selected as the mucoadhesive polymer. α-Mangostin was incorporated into the CS-SH/PVA solution and electrospun to obtain nanofiber mats. Scanning electron microscopy, differential scanning calorimetry, X-ray diffraction, and tensile strength testing were used to characterize the mats. The swelling degree and mucoadhesion were also determined. The nanofiber mats were further evaluated regarding their α-mangostin content, in vitro α-mangostin release, antibacterial activity, cytotoxicity, in vivo performance, and stability. The results indicated that the mats were in the nanometer range. The α-mangostin was well incorporated into the mats, with an amorphous form. The mats showed suitable tensile strength, swelling, and mucoadhesive properties. The loading capacity increased when the initial amount of α-mangostin was increased. Rapid release of α-mangostin from the mats was achieved. Additionally, a fast bacterial killing rate occurred at the lowest concentration of nanofiber mats when α-mangostin was added to the mats. The mats were less cytotoxic after use for 72 h. Moreover, in vivo testing indicated that the mats could reduce the number of oral bacteria, with a good mouth feel. The mats maintained the amount of α-mangostin for 6 months. The results suggest that α-mangostin-loaded mucoadhesive electrospun nanofiber mats may be a promising material for oral care and the prevention of dental caries.

Immobilization of CoCl2 (cobalt chloride) on PAN (polyacrylonitrile) composite nanofiber mesh filled with carbon nanotubes for hydrogen production from hydrolysis of NaBH4 (sodium borohydride)

International Nuclear Information System (INIS)

Li, Fang; Arthur, Ernest Evans; La, Dahye; Li, Qiming; Kim, Hern

2014-01-01

Composite nanofiber sheets containing multiwalled carbon nanotubes and cobalt chloride dispersed in PAN (polyacrylonitrile) were produced by an electrospinning technique. The synthesized PAN/CoCl 2 /CNTs composite nanofiber was used as the catalyst for hydrogen production from the hydrolysis of sodium borohydride. FT-IR characterization showed that the pretreated CNTs possess different organic functional groups which help improve the compatibility between CNTs and PAN organic polymer. SEM (scanning electron microscopy), TEM (transmission electron microscopy) and EDX (energy-dispersive X-ray technique) were used to characterize the composite nanofiber and it was found that CNTs can be coaxially dispersed into the PAN nanofiber. During the hydrolysis of NaBH 4 , this PAN/CoCl 2 /CNTs composite nanofiber exhibited higher catalytic activity compared to the composite without CNTs doping. Kinetic analysis of NaBH 4 hydrolysis shows that the reaction of NaBH 4 hydrolysis based on this catalyst can be ascribed to the first-order reaction and the activation energy of the catalyst was approximately 52.857 kJ/mol. Meanwhile, the composite nanofiber catalyst shows excellent stability and reusability in the recycling experiment. - Highlights: • Composite nanofiber sheets were prepared via electrospinning. • PAN (polyacrylonitrile)/CoCl 2 (cobalt chloride)/CNTs (carbon nanotubes) nanofiber was used as the catalyst for hydrogen production. • CNTs can be coaxially dispersed into the PAN nanofiber. • PAN/CoCl 2 /CNTs composite nanofiber exhibited higher catalytic activity. • The composite nanofiber catalyst shows excellent stability and reusability

Carbon nanofibers obtained from electrospinning process

Science.gov (United States)

Bovi de Oliveira, Juliana; Müller Guerrini, Lília; Sizuka Oishi, Silvia; Rogerio de Oliveira Hein, Luis; dos Santos Conejo, Luíza; Cerqueira Rezende, Mirabel; Cocchieri Botelho, Edson

2018-02-01

In recent years, reinforcements consisting of carbon nanostructures, such as carbon nanotubes, fullerenes, graphenes, and carbon nanofibers have received significant attention due mainly to their chemical inertness and good mechanical, electrical and thermal properties. Since carbon nanofibers comprise a continuous reinforcing with high specific surface area, associated with the fact that they can be obtained at a low cost and in a large amount, they have shown to be advantageous compared to traditional carbon nanotubes. The main objective of this work is the processing of carbon nanofibers, using polyacrylonitrile (PAN) as a precursor, obtained by the electrospinning process via polymer solution, with subsequent use for airspace applications as reinforcement in polymer composites. In this work, firstly PAN nanofibers were produced by electrospinning with diameters in the range of (375 ± 85) nm, using a dimethylformamide solution. Using a furnace, the PAN nanofiber was converted into carbon nanofiber. Morphologies and structures of PAN and carbon nanofibers were investigated by scanning electron microscopy, Raman Spectroscopy, thermogravimetric analyses and differential scanning calorimeter. The resulting residual weight after carbonization was approximately 38% in weight, with a diameters reduction of 50%, and the same showed a carbon yield of 25%. From the analysis of the crystalline structure of the carbonized material, it was found that the material presented a disordered structure.

One-pot electrospinning and gas-sensing properties of LaMnO3 perovskite/SnO2 heterojunction nanofibers

Science.gov (United States)

Chen, Dongdong; Yi, Jianxin

2018-03-01

Using nanostructured composite materials is an effective way to obtain high-performance gas sensors. This work used p-type LaMnO3 perovskite-structured semiconductor as a novel promoter for SnO2 nanofibers and studied the gas-sensing characteristics. Nanofibers of 0-2.5-mol% LaMnO3/SnO2 were synthesized via one-pot electrospinning. Compared with pristine SnO2, LaMnO3/SnO2 composite nanofibers exhibited smaller particle size (10-30 nm) and higher BET surface area. XPS revealed that oxygen surface absorption decreased with increasing LaMnO3 content. 0.3-mol% LaMnO3/SnO2 exhibited significantly enhanced ethanol sensitivity relative to pristine SnO2. A response of 20 was obtained at the optimum temperature of 260 °C for 100-ppm ethanol. Higher LaMnO3 loading led to decrease of the ethanol response. The impact of LaMnO3 loading on the sensing behavior of SnO2 nanofibers was discussed in terms of p-n heterojunction formation and changes in the microstructure and catalytic properties.

UV-responsive polyvinyl alcohol nanofibers prepared by electrospinning

Energy Technology Data Exchange (ETDEWEB)

Khatri, Zeeshan, E-mail: zeeshan.khatri@faculty.muet.edu.pk [Department of Textile Engineering, Mehran University of Engineering and Technology, Jamshoro 76062 (Pakistan); Nano Fusion Technology Research Lab, Division of Frontier Fibers, Institute for Fiber Engineering (IFES), Interdisciplinary Cluster for Cutting Edge Research (ICCER), Shinshu University, 3-15-1, Tokida, Ueda, Nagano 386-8567 (Japan); Ali, Shamshad [Department of Textile Engineering, Mehran University of Engineering and Technology, Jamshoro 76062 (Pakistan); Department of Organic and Nano Engineering, Hanyang University, 17 Haengdang-dong, Seongdong-gu, Seoul 133-791 (Korea, Republic of); Khatri, Imran [Department of Entomology, Sindh Agriculture University, Tandojam (Pakistan); Mayakrishnan, Gopiraman [Nano Fusion Technology Research Lab, Division of Frontier Fibers, Institute for Fiber Engineering (IFES), Interdisciplinary Cluster for Cutting Edge Research (ICCER), Shinshu University, 3-15-1, Tokida, Ueda, Nagano 386-8567 (Japan); Kim, Seong Hun [Department of Organic and Nano Engineering, Hanyang University, 17 Haengdang-dong, Seongdong-gu, Seoul 133-791 (Korea, Republic of); Kim, Ick-Soo, E-mail: kim@shinshu-u.ac.jp [Nano Fusion Technology Research Lab, Division of Frontier Fibers, Institute for Fiber Engineering (IFES), Interdisciplinary Cluster for Cutting Edge Research (ICCER), Shinshu University, 3-15-1, Tokida, Ueda, Nagano 386-8567 (Japan)

2015-07-01

Graphical abstract: - Highlights: • UV responsive PVA nanofibers were prepared via electrospinning. • Quick response codes were recorded multiple times on UV responsive nanofibers. • The rate of photo-coloration was found faster than the rate of photo-reversibility. - Abstract: We report UV-responsive polyvinyl alcohol (PVA) nanofibers for potential application for recording and erasing quick response (QR) codes. We incorporate 1′-3′-dihydro-8-methoxy-1′,3′,3′-trimethyl-6-nitrospiro [2H-1-benzopyran-2,2′-(2H)-indole] (indole) and,3-dihydro-1,3,3-trimethylspiro [2H-indole-2,3′-[3H] phenanthr [9,10-b] (1,4) oxazine] (oxazine) into PVA polymer matrix via electrospinning technique. The resultant nanofibers were measured for recording–erasing, photo-coloration and thermal reversibility. The rate of photo-coloration of PVA–indole nanofibers was five times higher than the PVA–oxazine nanofibers, whereas the thermal reversibility found to be more than twice as fast as PVA–oxazine nanofibers. Results showed that the resultant nanofibers have very good capability of recording QR codes multiple times. The FTIR spectroscopy and SEM were employed to characterize the electrospun nanofibers. The UV-responsive PVA nanofibers have great potentials as a light-driven nanomaterials incorporated within sensors, sensitive displays and in optical devices such as erasable and rewritable optical storage.

UV-responsive polyvinyl alcohol nanofibers prepared by electrospinning

International Nuclear Information System (INIS)

Khatri, Zeeshan; Ali, Shamshad; Khatri, Imran; Mayakrishnan, Gopiraman; Kim, Seong Hun; Kim, Ick-Soo

2015-01-01

Graphical abstract: - Highlights: • UV responsive PVA nanofibers were prepared via electrospinning. • Quick response codes were recorded multiple times on UV responsive nanofibers. • The rate of photo-coloration was found faster than the rate of photo-reversibility. - Abstract: We report UV-responsive polyvinyl alcohol (PVA) nanofibers for potential application for recording and erasing quick response (QR) codes. We incorporate 1′-3′-dihydro-8-methoxy-1′,3′,3′-trimethyl-6-nitrospiro [2H-1-benzopyran-2,2′-(2H)-indole] (indole) and,3-dihydro-1,3,3-trimethylspiro [2H-indole-2,3′-[3H] phenanthr [9,10-b] (1,4) oxazine] (oxazine) into PVA polymer matrix via electrospinning technique. The resultant nanofibers were measured for recording–erasing, photo-coloration and thermal reversibility. The rate of photo-coloration of PVA–indole nanofibers was five times higher than the PVA–oxazine nanofibers, whereas the thermal reversibility found to be more than twice as fast as PVA–oxazine nanofibers. Results showed that the resultant nanofibers have very good capability of recording QR codes multiple times. The FTIR spectroscopy and SEM were employed to characterize the electrospun nanofibers. The UV-responsive PVA nanofibers have great potentials as a light-driven nanomaterials incorporated within sensors, sensitive displays and in optical devices such as erasable and rewritable optical storage

Templates for integrated nanofiber growth

DEFF Research Database (Denmark)

Oliveira Hansen, Roana Melina de

the growth direction and the nanofiber length and position can be controlled by placement of nano-structured lines on the substrate. These lines can be used to guide the surface diffusion and thereby steer the self-assembly process of the organic molecules leading to morphologically well-defined molecular...... the morphology of the resulting structures leading to notably different electrical properties. The transistor design influences its electrical characteristics, and the top-gate configuration shows to have the stronger gate effect. In addition, platforms for light-emitting devices were fabricated......Para-hexaphenylene (p6P) molecules have the ability to self-assemble into organic nanofibers. These nanofibers hold unique optoelectronic properties, which make them interesting candidates as elements in electronic and optoelectronic devices. Typically these nanofibers are grown on specific single...

Antibacterial properties of laser spinning glass nanofibers.

Science.gov (United States)

Echezarreta-López, M M; De Miguel, T; Quintero, F; Pou, J; Landin, M

2014-12-30

A laser-spinning technique has been used to produce amorphous, dense and flexible glass nanofibers of two different compositions with potential utility as reinforcement materials in composites, fillers in bone defects or scaffolds (3D structures) for tissue engineering. Morphological and microstructural analyses have been carried out using SEM-EDX, ATR-FTIR and TEM. Bioactivity studies allow the nanofibers with high proportion in SiO2 (S18/12) to be classified as a bioinert glass and the nanofibers with high proportion of calcium (ICIE16) as a bioactive glass. The cell viability tests (MTT) show high biocompatibility of the laser spinning glass nanofibers. Results from the antibacterial activity study carried out using dynamic conditions revealed that the bioactive glass nanofibers show a dose-dependent bactericidal effect on Sthaphylococcus aureus (S. aureus) while the bioinert glass nanofibers show a bacteriostatic effect also dose-dependent. The antibacterial activity has been related to the release of alkaline ions, the increase of pH of the medium and also the formation of needle-like aggregates of calcium phosphate at the surface of the bioactive glass nanofibers which act as a physical mechanism against bacteria. The antibacterial properties give an additional value to the laser-spinning glass nanofibers for different biomedical applications, such as treating or preventing surgery-associated infections. Copyright © 2014 Elsevier B.V. All rights reserved.

Multi-scale carbon micro/nanofibers-based adsorbents for protein immobilization

Energy Technology Data Exchange (ETDEWEB)

Singh, Shiv; Singh, Abhinav [Department of Chemical Engineering, Indian Institute of Technology Kanpur, Kanpur 208016 (India); Bais, Vaibhav Sushil Singh; Prakash, Balaji [Department of Biological Science and Bioengineering, Indian Institute of Technology Kanpur, Kanpur 208016 (India); Verma, Nishith, E-mail: nishith@iitk.ac.in [Department of Chemical Engineering, Indian Institute of Technology Kanpur, Kanpur 208016 (India); Center for Environmental Science and Engineering, Indian Institute of Technology Kanpur, Kanpur 208016 (India)

2014-05-01

In the present study, different proteins, namely, bovine serum albumin (BSA), glucose oxidase (GOx) and the laboratory purified YqeH were immobilized in the phenolic resin precursor-based multi-scale web of activated carbon microfibers (ACFs) and carbon nanofibers (CNFs). These biomolecules are characteristically different from each other, having different structure, number of parent amino acid molecules and isoelectric point. CNF was grown on ACF substrate by chemical vapor deposition, using Ni nanoparticles (Nps) as the catalyst. The ultra-sonication of the CNFs was carried out in acidic medium to remove Ni Nps from the tip of the CNFs to provide additional active sites for adsorption. The prepared material was directly used as an adsorbent for proteins, without requiring any additional treatment. Several analytical techniques were used to characterize the prepared materials, including scanning electron microscopy, Fourier transform infrared spectroscopy, BET surface area, pore-size distribution, and UV–vis spectroscopy. The adsorption capacities of prepared ACFs/CNFs in this study were determined to be approximately 191, 39 and 70 mg/g for BSA, GOx and YqeH, respectively, revealing that the carbon micro-nanofibers forming synthesized multi-scale web are efficient materials for the immobilization of protein molecules. - Highlights: • Ni metal Np-dispersed carbon micro-nanofibers (ACFs/CNFs) are prepared. • ACFs/CNFs are mesoporous. • Significant adsorption of BSA, GOx and YqeH is observed on ACFs/CNFs. • Multi-scale web of ACFs/CNFs is effective for protein immobilization.

Printed second harmonic active organic nanofiber arrays

DEFF Research Database (Denmark)

Balzer, Frank; Brewer, Jonathan R.; Kjelstrup-Hansen, Jakob

2007-01-01

Organic nanofibers from semiconducting conjugated molecules are well suited to meet refined demands for advanced applications in future optoelectronics and nanophotonics. In contrast to their inorganic counterparts, the properties of organic nanowires can be tailored at the molecular level...... investigated nanofibers as grown via organic epitaxy. In the present work we show how chemically changing the functionalizing end groups leads to a huge increase of second order susceptibility, making the nanofibers technologically very interesting as efficient frequency doublers. For that the nanofibers have...

Synthesis and optimization of Ag–TiO2 composite nanofibers for photocatalytic treatment of impaired water sources

International Nuclear Information System (INIS)

Nalbandian, Michael J.; Zhang, Miluo; Sanchez, Joel; Kim, Seil; Choa, Yong-Ho; Cwiertny, David M.; Myung, Nosang V.

2015-01-01

Highlights: • We synthesized tunable Ag–TiO 2 nanofibers via electrospinning. • We examined property changes due to the addition of the co-catalyst Ag. • Photocatalytic activity against phenol was studied under UV irradiation. • The 0.5 at.% Ag–TiO 2 showed optimal photocatalytic activity. • The enhanced performance was associated with electron trap mechanism. - Abstract: In this work, Ag–TiO 2 composite nanofibers were fabricated by electrospinning, where the composition and crystallinity were tuned by controlling the precursor composition and annealing conditions. Characterization revealed that bulk–embedded Ag nanoparticles inhibited anatase-to-rutile phase transformation and a decrease in band gap from 3.2 down to 2.8 eV with increase in the Ag content. The photocatalytic activity of 0.5 at.% Ag–TiO 2 nanofibers toward phenol degradation was the greatest, outperforming both unmodified TiO 2 nanofibers and commercially available TiO 2 Aeroxide ® P25 by a factor of ∼3. The high reactivity of the low content Ag–TiO 2 nanofibers can be attributed to the addition of electron traps, which provide efficient carrier separation and, therefore, decreased recombination. However, further increase in Ag content led to lower photoreactivity, most likely due to the growth of the Ag nanoparticles, which suggests an optimal size of 2 to 3 nm for the Ag nanoparticles at 0.5 at.% provided the greatest photoreactivity. Ag–TiO 2 nanofibers show great promise as innovative and highly performing nanomaterials for future nanotechnology-based treatment systems, particularly when the photoreactivity demonstrate herein is used in synergy with the established antimicrobial activity of nano-Ag.

Fabrication of Carbon Nanotube Polymer Actuator Using Nanofiber Sheet

Science.gov (United States)

Kato, Hayato; Shimizu, Akikazu; Sato, Taiga; Kushida, Masahito

2017-11-01

Carbon nanotube polymer actuators were developed using composite nanofiber sheets fabricated by multi-walled carbon nanotubes(MWCNTs) and poly (vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP). Nanofiber sheets were fabricated by electrospinning method. The effect of flow rate and polymer concentration on nanofiber formation were verified for optimum condition for fabricating nanofiber sheets. We examined the properties of MWCNT/PVDF-HFP nanofiber sheets, as follows. Electrical conductivity and mechanical strength increased as the MWCNT weight ratio increased. We fabricated carbon nanotube polymer actuators using MWCNT/PVDF-HFP nanofiber sheets and succeeded in operating of our actuators.

A hybrid nanostructure of platinum-nanoparticles/graphitic-nanofibers as a three-dimensional counter electrode in dye-sensitized solar cells.

Science.gov (United States)

Hsieh, Chien-Kuo; Tsai, Ming-Chi; Su, Ching-Yuan; Wei, Sung-Yen; Yen, Ming-Yu; Ma, Chen-Chi M; Chen, Fu-Rong; Tsai, Chuen-Horng

2011-11-07

We directly synthesized a platinum-nanoparticles/graphitic-nanofibers (PtNPs/GNFs) hybrid nanostructure on FTO glass. We applied this structure as a three-dimensional counter electrode in dye-sensitized solar cells (DSSCs), and investigated the cells' photoconversion performance. This journal is © The Royal Society of Chemistry 2011

Self-assembled Bi{sub 2}MoO{sub 6}/TiO{sub 2} nanofiber heterojunction film with enhanced photocatalytic activities

Energy Technology Data Exchange (ETDEWEB)

Li, Hua [School of Chemical Engineering, Northwest University, Xi’an 710069 (China); Zhang, Tianxi [School of Physics, Northwest University, Xi’an 710069 (China); Pan, Chao; Pu, Chenchen; Hu, Yang [School of Chemical Engineering, Northwest University, Xi’an 710069 (China); Hu, Xiaoyun [School of Physics, Northwest University, Xi’an 710069 (China); Liu, Enzhou, E-mail: liuenzhou@nwu.edu.cn [School of Chemical Engineering, Northwest University, Xi’an 710069 (China); Fan, Jun, E-mail: fanjun@nwu.edu.cn [School of Chemical Engineering, Northwest University, Xi’an 710069 (China)

2017-01-01

Highlights: • Self-assembled Bi{sub 2}MoO{sub 6}/TiO{sub 2} nanofiber film was synthesized. • TiO{sub 2} nanofiber film exhibits excellent visible light scattering property. • The scattering light from TiO{sub 2} overlaps with the absorption light of Bi{sub 2}MoO{sub 6}. • Bi{sub 2}MoO{sub 6}/TiO{sub 2} heterojunction photocatalysts show higher photocatalytic activity. - Abstract: TiO{sub 2} nanofiber film (TiO{sub 2} NFF) was successfully fabricated by an ethylene glycol-assisted hydrothermal method, and then self-assembled flake-like Bi{sub 2}MoO{sub 6} was grown on the surface of TiO{sub 2} nanofiber under alcohol thermal condition. The investigations indicate that the nanofiber structure of TiO{sub 2} films exhibits excellent visible light scattering property, the scattering light overlaps with the absorption band of Bi{sub 2}MoO{sub 6}, which can enhance the utility of incident light. The prepared Bi{sub 2}MoO{sub 6}/TiO{sub 2} composites show obviously enhanced photocatalytic activity for methylene blue (MB) degradation compared with pure TiO{sub 2} nanofiber under visible light irradiation (λ > 420 nm). The enhanced photocatalytic activity is primarily attributed to the synergistic effect of visible light absorption and effective electron-hole separation at the interfaces of the two semiconductors, which is confirmed by photoluminescence (PL) and electrochemical tests.

Thermal conductivity of electrospun polyethylene nanofibers.

Science.gov (United States)

Ma, Jian; Zhang, Qian; Mayo, Anthony; Ni, Zhonghua; Yi, Hong; Chen, Yunfei; Mu, Richard; Bellan, Leon M; Li, Deyu

2015-10-28

We report on the structure-thermal transport property relation of individual polyethylene nanofibers fabricated by electrospinning with different deposition parameters. Measurement results show that the nanofiber thermal conductivity depends on the electric field used in the electrospinning process, with a general trend of higher thermal conductivity for fibers prepared with stronger electric field. Nanofibers produced at a 45 kV electrospinning voltage and a 150 mm needle-collector distance could have a thermal conductivity of up to 9.3 W m(-1) K(-1), over 20 times higher than the typical bulk value. Micro-Raman characterization suggests that the enhanced thermal conductivity is due to the highly oriented polymer chains and enhanced crystallinity in the electrospun nanofibers.

Fabrication of nanofiber mats from electrospinning of functionalized polymers

Science.gov (United States)

Oktay, Burcu; Kayaman-Apohan, Nilhan; Erdem-Kuruca, Serap

2014-08-01

Electrospinning technique enabled us to prepare nanofibers from synthetic and natural polymers. In this study, it was aimed to fabricate electrospun poly(vinyl alcohol) (PVA) based nanofibers by reactive electrospinning process. To improve endurance of fiber toward to many solvents, PVA was functionalized with photo-crosslinkable groups before spinning. Afterward PVA was crosslinked by UV radiation during electrospinning process. The nanofiber mats were characterized by scanning electron microscopy (SEM). The results showed that homogenous, uniform and crosslinked PVA nanofibers in diameters of about 200 nm were obtained. Thermal stability of the nanofiber mat was investigated with thermal gravimetric analysis (TGA). Also the potential use of this nanofiber mats for tissue engineering was examined. Osteosarcoma (Saos) cells were cultured on the nanofiber mats.

Fabrication of nanofiber mats from electrospinning of functionalized polymers

International Nuclear Information System (INIS)

Oktay, Burcu; Kayaman-Apohan, Nilhan; Erdem-Kuruca, Serap

2014-01-01

Electrospinning technique enabled us to prepare nanofibers from synthetic and natural polymers. In this study, it was aimed to fabricate electrospun poly(vinyl alcohol) (PVA) based nanofibers by reactive electrospinning process. To improve endurance of fiber toward to many solvents, PVA was functionalized with photo-crosslinkable groups before spinning. Afterward PVA was crosslinked by UV radiation during electrospinning process. The nanofiber mats were characterized by scanning electron microscopy (SEM). The results showed that homogenous, uniform and crosslinked PVA nanofibers in diameters of about 200 nm were obtained. Thermal stability of the nanofiber mat was investigated with thermal gravimetric analysis (TGA). Also the potential use of this nanofiber mats for tissue engineering was examined. Osteosarcoma (Saos) cells were cultured on the nanofiber mats

Growth of Y-shaped Carbon Nanofibers from Ethanol Flames

Directory of Open Access Journals (Sweden)

Cheng Jin

2008-01-01

Full Text Available Abstract Y-shaped carbon nanofibers as a multi-branched carbon nanostructure have potential applications in electronic devices. In this article, we report that several types of Y-shaped carbon nanofibers are obtained from ethanol flames. These Y-shaped carbon nanofibers have different morphologies. According to our experimental results, the growth mechanism of Y-shaped carbon nanofibers has been discussed and a possible growth model of Y-shaped carbon nanofibers has been proposed.

Bioactive thermoresponsive polyblend nanofiber formulations for wound healing

Energy Technology Data Exchange (ETDEWEB)

Pawar, Mahesh D. [Polymer Science and Engineering, National Chemical Laboratory, Homi Bhabha Road, Pashan, Pune 411008 (India); MAEER' s Maharashtra Institute of Pharmacy S. No. 124, MIT Campus Paud Road, Kothrud, Pune 411 038 (India); Rathna, G.V.N., E-mail: rv.gundloori@ncl.res.in [Polymer Science and Engineering, National Chemical Laboratory, Homi Bhabha Road, Pashan, Pune 411008 (India); Agrawal, Shubhang [Polymer Science and Engineering, National Chemical Laboratory, Homi Bhabha Road, Pashan, Pune 411008 (India); Kuchekar, Bhanudas S. [MAEER' s Maharashtra Institute of Pharmacy S. No. 124, MIT Campus Paud Road, Kothrud, Pune 411 038 (India)

2015-03-01

The rationale of this work is to develop new bioactive thermoresponsive polyblend nanofiber formulations for wound healing (topical). Various polymer compositions of thermoresponsive, poly(N-isopropylacrylamide), egg albumen and poly(ε-caprolactone) blend solutions with and without a drug [gatifloxacin hydrochloride, Gati] were prepared. Non-woven nanofibers of various compositions were fabricated using an electrospinning technique. The morphology of the nanofibers was analyzed by an environmental scanning electron microscope. The morphology was influenced by the concentration of polymer, drug, and polymer blend composition. Fourier transform infrared spectroscopy analysis showed the shift in bands due to hydrogen ion interactions between polymers and drug. Thermogram of PNIPAM/PCL/EA with Gati recorded a shift in lower critical solution temperature (LCST) and glass transition temperature (T{sub g}) of PNIPAM. Similarly T{sub g} and melting temperature (T{sub m}) of PCL were shifted. X-ray diffraction patterns recorded a decrease in the crystalline state of PCL nanofibers and transformed crystalline drug to an amorphous state. In vitro release study of nanofibers with Gati showed initial rapid release up to 10 h, followed by slow and controlled release for 696 h (29 days). Nanofiber mats with Gati exhibited antibacterial properties to Staphylococcus aureus, supported suitable controlled drug release with in vitro cell viability and in vivo wound healing. - Highlights: • Thermoresponsive and bioactive nanofiber blends of PNIPAM/EA/PCL were fabricated. • Nanofiber blends favored initial rapid release, followed by controlled release. • In vitro cell viability of pure polymers and nanofiber blends was least toxic. • In vivo studies of drug loaded nanofiber mats recorded faster tissue regeneration.

Development and characterization of highly oriented PAN nanofiber

Directory of Open Access Journals (Sweden)

M. Sadrjahani

2010-12-01

Full Text Available A simple and non-conventional electrospinning technique was employed for producing highly oriented Polyacrylonitrile (PAN nanofibers. The PAN nanofibers were electrospun from 14 wt% solution of PAN in dimethylformamid (DMF at 11 kv on a rotating drum with various linear speeds from 22.5 m/min to 67.7 m/min. The influence of take up velocity was investigated on the degree of alignment, internal structure and mechanical properties of collected PAN nanofibers. Using an image processing technique, the best degree of alignment was obtained for those nanofibers collected at a take up velocity of 59.5 m/min. Moreover, Raman spectroscopy was used for measuring molecular orientation of PAN nanofibers. Similarly, a maximum chain orientation parameter of 0.25 was determined for nanofibers collected at a take up velocity of 59.5 m/min.

Facile Synthesis of Coaxial CNTs/MnOx-Carbon Hybrid Nanofibers and Their Greatly Enhanced Lithium Storage Performance.

Science.gov (United States)

Yang, Zunxian; Lv, Jun; Pang, Haidong; Yan, Wenhuan; Qian, Kun; Guo, Tailiang; Guo, Zaiping

2015-12-01

Carbon nanotubes (CNTs)/MnOx-Carbon hybrid nanofibers have been successfully synthesized by the combination of a liquid chemical redox reaction (LCRR) and a subsequent carbonization heat treatment. The nanostructures exhibit a unique one-dimensional core/shell architecture, with one-dimensional CNTs encapsulated inside and a MnOx-carbon composite nanoparticle layer on the outside. The particular porous characteristics with many meso/micro holes/pores, the highly conductive one-dimensional CNT core, as well as the encapsulating carbon matrix on the outside of the MnOx nanoparticles, lead to excellent electrochemical performance of the electrode. The CNTs/MnOx-Carbon hybrid nanofibers exhibit a high initial reversible capacity of 762.9 mAhg(-1), a high reversible specific capacity of 560.5 mAhg(-1) after 100 cycles, and excellent cycling stability and rate capability, with specific capacity of 396.2 mAhg(-1) when cycled at the current density of 1000 mAg(-1), indicating that the CNTs/MnOx-Carbon hybrid nanofibers are a promising anode candidate for Li-ion batteries.

Graphene oxide decorated electrospun gelatin nanofibers: Fabrication, properties and applications

Energy Technology Data Exchange (ETDEWEB)

Jalaja, K. [Department of Chemistry, Indian Institute of Space Science and Technology, Valiamala, Thiruvananthapuram, Kerala 695 547 (India); Sreehari, V.S. [Indian Institute of Science Education and Research Bhopal, Bhauri, Madhya Pradesh 462066 (India); Kumar, P.R. Anil [Tissue culture laboratory, Biomedical Technology Wing, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Poojappura, Thiruvananthapuram, Kerala 695 012 (India); Nirmala, R. James, E-mail: nirmala@iist.ac.in [Department of Chemistry, Indian Institute of Space Science and Technology, Valiamala, Thiruvananthapuram, Kerala 695 547 (India)

2016-07-01

Gelatin nanofiber fabricated by electrospinning process is found to mimic the complex structural and functional properties of natural extracellular matrix for tissue regeneration. In order to improve the physico-chemical and biological properties of the nanofibers, graphene oxide is incorporated in the gelatin to form graphene oxide decorated gelatin nanofibers. The current research effort is focussed on the fabrication and evaluation of physico-chemical and biological properties of graphene oxide-gelatin composite nanofibers. The presence of graphene oxide in the nanofibers was established by transmission electron microscopy (TEM). We report the effect of incorporation of graphene oxide on the mechanical, thermal and biological performance of the gelatin nanofibers. The tensile strength of gelatin nanofibers was increased from 8.29 ± 0.53 MPa to 21 ± 2.03 MPa after the incorporation of GO. In order to improve the water resistance of nanofibers, natural based cross-linking agent, namely, dextran aldehyde was employed. The cross-linked composite nanofibers showed further increase in the tensile strength up to 56.4 ± 2.03 MPa. Graphene oxide incorporated gelatin nanofibers are evaluated for bacterial activity against gram positive (Staphylococcus aureus) and gram negative (Escherichia coli) bacteria and cyto compatibility using mouse fibroblast cells (L-929 cells). The results indicate that the graphene oxide incorporated gelatin nanofibers do not prevent bacterial growth, nevertheless support the L-929 cell adhesion and proliferation. - Highlights: • Graphene oxide nano reinforced gelatin nanofibers are fabricated by electrospinning. • Graphene oxide (0.5%) loading resulted in increased tensile strength. • GO/gelatin nanofibers are cross-linked with dextran aldehyde. • Composite nanofibers favoured adhesion of L-929 cells. • GO/gelatin mats do not prevent bacterial growth.

Synthesis and photocatalytic properties of graphitic carbon nitride nanofibers using porous anodic alumina templates

Science.gov (United States)

Suchitra, S. M.; Udayashankar, N. K.

2017-12-01

In the present study, we describe an effective method for the synthesis of Graphitic carbon nitride (GCN) nanostructures using porous anodic alumina (AAO) membrane as template by simple thermal condensation of cyanamide. Synthesized nanostructure was fully analysed by various techniques to detect its crystalline nature, morphology, luminescent properties followed by the evaluation of its photocatalytic activity in the degradation of Methylene blue dye. Structural analysis of synthesized GCNNF was systematically carried out using x-ray powder diffraction (XRD) and scanning electron microscope (SEM), and. The results confirmed the growth of GCN inside the nanochannels of anodic alumina templates. Luminescent properties of GCNNF were studied using photoluminescence (PL) spectroscopy. PL analysis showed the presence of a strong emission peak in the wavelength range of 350-600 nm in blue region. GCNNF displays higher photocatalytic performance in the photodegradation of methylene blue compare to the bulk GCN. Highlights 1. In the present paper, we report the synthesis of graphitic carbon nitride nanofibers (GCNNF) using porous anodic aluminium oxide membranes as templates through thermal condensation of cyanamide at 500 °C. 2. The synthesis of Graphitic carbon nitride nanofibers using porous andic alumina template is the efficient approach for increasing crystallinity and surface area. 3. The high surface area of graphitic carbon nitride nanofibers has a good impact on novel optical and photocatalytic properties of the bulkGCN. 4. AAO templating of GCN is one of the versatile method to produce tailorable GCN nanostructures with higher surface area and less number of structural defects. 5. Towards photocatalytic degradation of dyes, the tuning of physical properties is very essential thing hence we are succeeded in achieving better catalytic performance of GCN nanostructures by making use of AAO templates.

Bioactive self-assembled peptide nanofibers for corneal stroma regeneration.

Science.gov (United States)

Uzunalli, G; Soran, Z; Erkal, T S; Dagdas, Y S; Dinc, E; Hondur, A M; Bilgihan, K; Aydin, B; Guler, M O; Tekinay, A B

2014-03-01

Defects in the corneal stroma caused by trauma or diseases such as macular corneal dystrophy and keratoconus can be detrimental for vision. Development of therapeutic methods to enhance corneal regeneration is essential for treatment of these defects. This paper describes a bioactive peptide nanofiber scaffold system for corneal tissue regeneration. These nanofibers are formed by self-assembling peptide amphiphile molecules containing laminin and fibronectin inspired sequences. Human corneal keratocyte cells cultured on laminin-mimetic peptide nanofibers retained their characteristic morphology, and their proliferation was enhanced compared with cells cultured on fibronectin-mimetic nanofibers. When these nanofibers were used for damaged rabbit corneas, laminin-mimetic peptide nanofibers increased keratocyte migration and supported stroma regeneration. These results suggest that laminin-mimetic peptide nanofibers provide a promising injectable, synthetic scaffold system for cornea stroma regeneration. Copyright © 2013 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

Electrospun polymeric nanofibers for transdermal drug delivery

Directory of Open Access Journals (Sweden)

Mahya Rahmani

2017-04-01

Full Text Available Conventional transdermal drug delivery systems (TDDS have been designed for drug delivery through the skin. These systems use the permeability property of stratum corneum, the outermost surface layer of the skin. Applying polymeric micro and nanofibers in drug delivery has recently attracted great attention and the electrospinning technique is the preferred method for polymeric micro-nanofibers fabrication with a great potential for drug delivery. More studies in the field of nanofibers containing drug are divided two categories: first, preparation and characterization of nanofibers containing drug and second, investigation of their therapeutic applications. Drugs used in electrospun nanofibers can be categorized into three main groups, including antibiotics and antimicrobial agents, anti-inflammatory agents and vitamins with therapeutic applications. In this paper, we review the application of electrospun polymeric scaffolds in TDDS and also introduce several pharmaceutical and therapeutic agents which have been used in polymer nanofibrous patches.

Investigation of needleless electrospun PAN nanofiber mats

Science.gov (United States)

Sabantina, Lilia; Mirasol, José Rodríguez; Cordero, Tomás; Finsterbusch, Karin; Ehrmann, Andrea

2018-04-01

Polyacrylonitrile (PAN) can be spun from a nontoxic solvent (DMSO, dimethyl sulfoxide) and is nevertheless waterproof, opposite to the biopolymers which are spinnable from aqueous solutions. This makes PAN an interesting material for electrospinning nanofiber mats which can be used for diverse biotechnological or medical applications, such as filters, cell growth, wound healing or tissue engineering. On the other hand, PAN is a typical base material for producing carbon nanofibers. Nevertheless, electrospinning PAN necessitates convenient spinning parameters to create nanofibers without too many membranes or agglomerations. Thus we have studied the influence of spinning parameters on the needleless electrospinning process of PAN dissolved in DMSO and the resulting nanofiber mats.

Piezoelectric Active Humidity Sensors Based on Lead-Free NaNbO3 Piezoelectric Nanofibers

Directory of Open Access Journals (Sweden)

Li Gu

2016-06-01

Full Text Available The development of micro-/nano-scaled energy harvesters and the self-powered sensor system has attracted great attention due to the miniaturization and integration of the micro-device. In this work, lead-free NaNbO3 piezoelectric nanofibers with a monoclinic perovskite structure were synthesized by the far-field electrospinning method. The flexible active humidity sensors were fabricated by transferring the nanofibers from silicon to a soft polymer substrate. The sensors exhibited outstanding piezoelectric energy-harvesting performance with output voltage up to 2 V during the vibration process. The output voltage generated by the NaNbO3 sensors exhibited a negative correlation with the environmental humidity varying from 5% to 80%, where the peak-to-peak value of the output voltage generated by the sensors decreased from 0.40 to 0.07 V. The sensor also exhibited a short response time, good selectively against ethanol steam, and great temperature stability. The piezoelectric active humidity sensing property could be attributed to the increased leakage current in the NaNbO3 nanofibers, which was generated due to proton hopping among the H3O+ groups in the absorbed H2O layers under the driving force of the piezoelectric potential.

Electrochemical fabrication and electronic behavior of polypyrrole nano-fiber array devices

International Nuclear Information System (INIS)

Liu Ling; Zhao Yaomin; Jia Nengqin; Zhou Qin; Zhao Chongjun; Yan Manming; Jiang Zhiyu

2006-01-01

Electrochemically active Polypyrrole (PPy) nano-fiber array device was fabricated via electrochemical deposition method using aluminum anodic oxide (AAO) membrane as template. After alkaline treatment electrochemically active PPy nano-fiber lost electrochemical activity, and became electrochemically inactive PPy. The electronic properties of PPy nano-fiber array devices were measured by means of a simple method. It was found that for an indium-tin oxide/electrochemically inactive PPy nano-fiber device, the conductivity of nano-fiber increased with the increase of voltage applied on the two terminals of nano-fiber. The electrochemical inactive PPy nano-fiber might be used as a nano-fiber switching diode. Both Au/electrochemically active PPy and Au/electrochemically inactive PPy nano-fiber devices demonstrate rectifying behavior, and might have been used for further application as nano-rectifiers

Electrochemical fabrication and electronic behavior of polypyrrole nano-fiber array devices

Energy Technology Data Exchange (ETDEWEB)

Ling, Liu [Department of Chemistry, and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433 (China); Yaomin, Zhao [Department of Chemistry, and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433 (China); Nengqin, Jia [Department of Chemistry, and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433 (China); Qin, Zhou [Department of Chemistry, and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433 (China); Chongjun, Zhao [Photon Craft Project, Shanghai Institute of Optics and Fine Mechanics, Chinese Academy of Sciences and Japan Science and Technology Agency, Shanghai 201800 (China); Manming, Yan [Department of Chemistry, and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433 (China); Zhiyu, Jiang [Department of Chemistry, and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai 200433 (China)

2006-05-01

Electrochemically active Polypyrrole (PPy) nano-fiber array device was fabricated via electrochemical deposition method using aluminum anodic oxide (AAO) membrane as template. After alkaline treatment electrochemically active PPy nano-fiber lost electrochemical activity, and became electrochemically inactive PPy. The electronic properties of PPy nano-fiber array devices were measured by means of a simple method. It was found that for an indium-tin oxide/electrochemically inactive PPy nano-fiber device, the conductivity of nano-fiber increased with the increase of voltage applied on the two terminals of nano-fiber. The electrochemical inactive PPy nano-fiber might be used as a nano-fiber switching diode. Both Au/electrochemically active PPy and Au/electrochemically inactive PPy nano-fiber devices demonstrate rectifying behavior, and might have been used for further application as nano-rectifiers.

A novel nano-nonwoven fabric with three-dimensionally dispersed nanofibers: entrapment of carbon nanofibers within nonwovens using the wet-lay process

International Nuclear Information System (INIS)

Karwa, Amogh N; Davis, Virginia A; Tatarchuk, Bruce J; Barron, Troy J

2012-01-01

This study demonstrates, for the first time, the manufacturing of novel nano-nonwovens that are comprised of three-dimensionally distributed carbon nanofibers within the matrices of traditional wet-laid nonwovens. The preparation of these nano-nonwovens involves dispersing and flocking carbon nanofibers, and optimizing colloidal chemistry during wet-lay formation. The distribution of nanofibers within the nano-nonwoven was verified using polydispersed aerosol filtration testing, air permeability, low surface tension liquid capillary porometry, SEM and cyclic voltammetry. All these characterization techniques indicated that nanofiber flocks did not behave as large solid clumps, but retained the ‘nanoporous’ structure expected from nanofibers. These nano-nonwovens showed significant enhancements in aerosol filtration performance. The reduction–oxidation reactions of the functional groups on nanofibers and the linear variation of electric double-layer capacitance with nanofiber loading were measured using cyclic voltammetry. More than 65 m 2 (700 ft 2 ) of the composite were made during the demonstration of process scalability using a Fourdrinier-type continuous pilot papermaking machine. The scalability of the process with the control over pore size distribution makes these composites very promising for filtration and other nonwoven applications. (paper)

Hydrothermal synthesis, characterization, and luminescence of Ca_2B_2O_5:RE (RE = Eu"3"+, Tb"3"+, Dy"3"+) nanofibers

International Nuclear Information System (INIS)

Yang, Li; Wan, Yingpeng; Li, Yuze; Pu, Yinfu; Huang, Yanlin; Chen, Cuili; Seo, Hyo Jin

2016-01-01

Ca_2B_2O_5:RE (RE = Eu"3"+, Tb"3"+, Dy"3"+) nanofibers were synthesized by the hydrothermal reaction method. The structural refinement was conducted on the base of the X-ray powder diffraction (XRD) measurements. The surface properties of the Ca_2B_2O_5:RE (RE = Eu"3"+, Tb"3"+, Dy"3"+) nanofibers were investigated by the measurements such as the scanning electron microscope (SEM), transmission electron microscope (TEM), and the energy dispersive spectrum (EDS). The nanofiber has a diameter of about 100 nm and a length of several micrometers. The luminescence properties such as photoluminescence excitation (PLE) and emission spectra (PL), decay lifetime, color coordinates, and the absolute internal quantum efficiency (QE) were reported. Ca_2B_2O_5:Eu"3"+ nanofibers show the red luminescence with CIE coordinates of (x = 0.41, y = 0.51) and the luminescence lifetime of 0.63 ms. The luminescence of Ca_2B_2O_5:Tb"3"+ nanofibers is green color (x = 0.29, y = 0.53) with the lifetime of 2.13 ms. However, Dy"3"+-doped Ca_2B_2O_5 nanofibers present a single-phase white-color phosphor with the fluorescence decay of 3.05 ms. Upon near-UV excitation, the absolute quantum efficiency is measured to be 65, 35, and 37 % for Eu"3"+-, Tb"3"+-, Dy"3"+-doped Ca_2B_2O_5 nanofibers, respectively. It is suggested that Ca_2B_2O_5:RE (RE = Eu"3"+, Tb"3"+, Dy"3"+) nanofibers could be an efficient phosphor for lighting and display.

One-step synthesis and characterization of polyaniline nanofiber/silver nanoparticle composite networks as antibacterial agents.

Science.gov (United States)

Poyraz, Selcuk; Cerkez, Idris; Huang, Tung Shi; Liu, Zhen; Kang, Litao; Luo, Jujie; Zhang, Xinyu

2014-11-26

Through a facile and effective seeding polymerization reaction via a one-step redox/complexation process, which took place in aqueous medium at ambient temperature, silver nanoparticles (Ag NPs) embedded polyaniline nanofiber (PANI NF) networks were synthesized as antibacterial agents. During the reaction, not only NF morphology formation of the resulting conducting polymers (CPs) but also amplification of the aqueous silver nitrate (AgNO3) solutions' oxidative potentials were managed by vanadium pentoxide (V2O5) sol-gel nanofibers, which acted as well-known nanofibrous seeding agents and the auxiliary oxidative agent at the same time. The PANI/Ag nanocomposites were proven to exhibit excellent antibacterial property against both Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus. Antibacterial property performance and average life span of the nanocomposite network were optimized through the homogeneous distribution/embedment of Ag NPs within one-dimensional (1-D) PANI NF matrix. The antibacterial efficacy tests and nanocomposite material characterization results further indicated that the sole components of PANI/Ag have a synergistic effect to each other in terms of antibacterial property. Thus, this well-known catalytic seeding approach via a one-step oxidative polymerization reaction can be considered as a general methodology and a substantial fabrication tool to synthesize Ag NP decorated nanofibrillar PANI networks as advanced antibacterial agents.

Novel-structured electrospun TiO2/CuO composite nanofibers for high efficient photocatalytic cogeneration of clean water and energy from dye wastewater.

Science.gov (United States)

Lee, Siew Siang; Bai, Hongwei; Liu, Zhaoyang; Sun, Darren Delai

2013-08-01

It is still a challenge to photocatalytically cogenerate clean water and energy from dye wastewater owing to the relatively low photocatalytic efficiency of photocatalysts. In this study, novel-structured TiO2/CuO composite nanofibers were successfully fabricated via facile electrospinning. For the first time, the TiO2/CuO composite nanofibers demonstrated multifunctional ability for concurrent photocatalytic organic degradation and H2 generation from dye wastewater. The enhanced photocatalytic activity of TiO2/CuO composite nanofibers was ascribed to its excellent synergy of physicochemical properties: 1) mesoporosity and large specific surface area for efficient substrate adsorption, mass transfer and light harvesting; 2) red-shift of the absorbance spectra for enhanced light utilization; 3) long nanofibrous structure for efficient charge transfer and ease of recovery, 4) TiO2/CuO heterojunctions which enhance the separation of electrons and holes and 5) presence of CuO which serve as co-catalyst for the H2 production. The TiO2/CuO composite nanofibers also exhibited rapid settleability by gravity and uncompromised reusability. Thus, the as-synthesized TiO2/CuO composite nanofibers represent a promising candidate for highly efficient concurrent photocatalytic organic degradation and clean energy production from dye wastewater. Copyright © 2013 Elsevier Ltd. All rights reserved.

Facile synthesis of ammonium vanadate nanofibers by using reflux in aqueous V{sub 2}O{sub 5} solution with ammonium persulfate

Energy Technology Data Exchange (ETDEWEB)

Lee, Se Hun [Department of Convergence Nanoscience, Hanyang University, 222 Wangsimni-ro, Seongdong-gu, Seoul 133-791 (Korea, Republic of); Koo, Jun Mo [Department of Organic and Nano Engineering, Hanyang University, 222 Wangsimni-ro, Seongdong-gu, Seoul 133-791 (Korea, Republic of); Oh, Seong Geun, E-mail: seongoh@hanyang.ac.kr [Department of Chemical Engineering, Hanyang University, 222 Wangsimni-ro, Seongdong-gu, Seoul 133-791 (Korea, Republic of); Im, Seung Soon, E-mail: imss007@hanyang.ac.kr [Department of Convergence Nanoscience, Hanyang University, 222 Wangsimni-ro, Seongdong-gu, Seoul 133-791 (Korea, Republic of); Department of Organic and Nano Engineering, Hanyang University, 222 Wangsimni-ro, Seongdong-gu, Seoul 133-791 (Korea, Republic of)

2017-06-15

Ammonium vanadate nanofibers were synthesized by simple reflux method in aqueous V{sub 2}O{sub 5} solution with ammonium persulfate without relying on surfactants, catalysts, harmful solvents and autoclave. The degree of intercalation by cationic ammonium ions into the crystal structure of vanadium oxide along with its change in chemical composition were analyzed by thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS), infrared spectroscopy (IR). The morphological changes toward nanofiber structure, having diameter of 20–30 nm and a few μm length, were investigated using transmission electron microscopy (TEM), scanning electron microscopy (SEM) and X-ray diffraction (XRD). The influences of synthetic conditions, such as reaction time and concentration of sulfate (SO{sub 4}{sup 2-}), on the crystal structures and morphologies of the resulting products have investigated. As a result, the ammonium vanadate nanofiber was formed in a short reaction time through a simple reflux method and yielded comparable electrical conductivity 1.47 × 10{sup -2} S/cm. - Highlights: • Ammonium vanadate nanofiber (AVFr) was prepared by simple reflux method. • AVFr yielded comparable electrical conductivity 1.47 × 10{sup -2} S/cm. • The electrical conductivity was improved by the increased amount of ammonium ion. • Sulfate ions (SO{sub 4}{sup 2-}) play a crucial role in controlling the morphology of nanofiber.

Silver/polysaccharide-based nanofibrous materials synthesized from green chemistry approach.

Science.gov (United States)

Martínez-Rodríguez, M A; Garza-Navarro, M A; Moreno-Cortez, I E; Lucio-Porto, R; González-González, V A

2016-01-20

In this contribution a novel green chemistry approach for the synthesis of nanofibrous materials based on blends of carboxymethyl-cellulose (CMC)-silver nanoparticles (AgNPs) composite and polyvinyl-alcohol (PVA) is proposed. These nanofibrous materials were obtained from the electrospinning of blends of aqueous solutions of CMC-AgNPs composite and PVA, which were prepared at different CMC/PVA weight ratios in order to electrospin nanofibers applying a constant tension of 15kV. The synthesized materials were characterized by means of transmission electron microscopy, scanning electron microscopy; as well as Fourier-transform infrared, ultraviolet and Raman spectroscopic techniques. Experimental evidence suggests that the diameter of the nanofibers is thinner than any other reported in the literature regarding the electrospinning of CMC. This feature is related to the interactions of AgNPs with carboxyl functional groups of the CMC, which diminish those between the later and acetyl groups of PVA. Copyright © 2015 Elsevier Ltd. All rights reserved.

Synthesis and optimization of Ag–TiO{sub 2} composite nanofibers for photocatalytic treatment of impaired water sources

Energy Technology Data Exchange (ETDEWEB)

Nalbandian, Michael J.; Zhang, Miluo; Sanchez, Joel [Department of Chemical and Environmental Engineering, University of California, Riverside, Riverside, CA 92521 (United States); Kim, Seil; Choa, Yong-Ho [Department of Fusion Chemical Engineering, Hanyang University, Ansan, Kyeonggi-do 426-791 (Korea, Republic of); Cwiertny, David M., E-mail: david-cwiertny@uiowa.edu [Department of Civil and Environmental Engineering, University of Iowa, Iowa, IA 52242 (United States); Myung, Nosang V., E-mail: myung@engr.ucr.edu [Department of Chemical and Environmental Engineering, University of California, Riverside, Riverside, CA 92521 (United States)

2015-12-15

Highlights: • We synthesized tunable Ag–TiO{sub 2} nanofibers via electrospinning. • We examined property changes due to the addition of the co-catalyst Ag. • Photocatalytic activity against phenol was studied under UV irradiation. • The 0.5 at.% Ag–TiO{sub 2} showed optimal photocatalytic activity. • The enhanced performance was associated with electron trap mechanism. - Abstract: In this work, Ag–TiO{sub 2} composite nanofibers were fabricated by electrospinning, where the composition and crystallinity were tuned by controlling the precursor composition and annealing conditions. Characterization revealed that bulk–embedded Ag nanoparticles inhibited anatase-to-rutile phase transformation and a decrease in band gap from 3.2 down to 2.8 eV with increase in the Ag content. The photocatalytic activity of 0.5 at.% Ag–TiO{sub 2} nanofibers toward phenol degradation was the greatest, outperforming both unmodified TiO{sub 2} nanofibers and commercially available TiO{sub 2} Aeroxide{sup ®} P25 by a factor of ∼3. The high reactivity of the low content Ag–TiO{sub 2} nanofibers can be attributed to the addition of electron traps, which provide efficient carrier separation and, therefore, decreased recombination. However, further increase in Ag content led to lower photoreactivity, most likely due to the growth of the Ag nanoparticles, which suggests an optimal size of 2 to 3 nm for the Ag nanoparticles at 0.5 at.% provided the greatest photoreactivity. Ag–TiO{sub 2} nanofibers show great promise as innovative and highly performing nanomaterials for future nanotechnology-based treatment systems, particularly when the photoreactivity demonstrate herein is used in synergy with the established antimicrobial activity of nano-Ag.

A novel non-enzymatic H2O2 sensor based on polypyrrole nanofibers-silver nanoparticles decorated reduced graphene oxide nano composites

Science.gov (United States)

Moozarm Nia, Pooria; Lorestani, Farnaz; Meng, Woi Pei; Alias, Y.

2015-03-01

Graphene oxide (GO) decorated with silver nanoparticles (AgNPs), was electrochemically reduced on glassy carbon electrode (GCE) by an amperometry method (AMP-AgNPs-rGO/GCE). Then, Pyrrole was electropolymerized on the surface of the modified electrode through amperometry process in order to obtain nanofibers of polypyrrole (AMP-PpyNFs-AgNPs-rGO). Fourier-transform infrared transmission spectroscopy and X-ray diffraction approved that during the amperometry process, the GO and Ppy nanofibers were reduced and polymerized respectively and the silver nanoparticles were formed. Field emission scanning electron microscope images indicated that the silver nanoparticles were homogeneously distributed on the rGO surface with a narrow nano size distribution and polypyrrole synthesized in the form of nanofibers with diameter around 100 nm. The first linear section was in the range of 0.1-5 mM with a limit of detection of 1.099 and the second linear section raised to 90 mM with a correlation factor of 0.085 (S/N of 3)

Advancement in organic nanofiber based transistors

DEFF Research Database (Denmark)

Jensen, Per Baunegaard With; Kjelstrup-Hansen, Jakob; Tavares, Luciana

and characterization of OLETs using the organic semiconductors para-hexaphenylene (p6P), 5,5´-Di-4-biphenyl-2,2´-bithiophene (PPTTPP) and 5,5'-bis(naphth-2-yl)-2,2'-bithiophene (NaT2). These molecules can self-assemble forming molecular crystalline nanofibers. Organic nanofibers can form the basis for light......The focus of this project is to study the light emission from nanofiber based organic light-emitting transistors (OLETs) with the overall aim of developing efficient, nanoscale light sources with different colors integrated on-chip. The research performed here regards the fabrication...

Multicolored Nanofiber Based Organic Light-Emitting Transistor

DEFF Research Database (Denmark)

With Jensen, Per Baunegaard; Kjelstrup-Hansen, Jakob; Tavares, Luciana

For optoelectronic applications, organic semiconductors have several advantages over their inorganic counterparts such as facile synthesis, tunability via synthetic chemistry, and low temperature processing. Self-assembled, molecular crystalline nanofibers are of particular interest as they could...... form ultra-small light-emitters in future nanophotonic applications. Such organic nanofibers exhibit many interesting optical properties including polarized photo- and electroluminescence, waveguiding, and emission color tunability. We here present a first step towards a multicolored, electrically...... driven device by combining nanofibers made from two different molecules, parahexaphenylene (p6P) and 5,5´-Di-4-biphenyl-2,2´-bithiophene (PPTTPP), which emits blue and green light, respectively. The organic nanofibers are implemented on a bottom gate/bottom contact field-effect transistor platform using...

Influence of thin film nickel pretreatment on catalytic thermal chemical vapor deposition of carbon nanofibers

Energy Technology Data Exchange (ETDEWEB)

Tiggelaar, R.M. [Mesoscale Chemical Systems, MESA" + Institute for Nanotechnology, University of Twente, P.O. Box 217, 7500 AE Enschede (Netherlands); Thakur, D.B.; Nair, H.; Lefferts, L.; Seshan, K. [Catalytic Processes and Materials, MESA" + Institute for Nanotechnology, University of Twente, P.O. Box 217, 7500 AE Enschede (Netherlands); Gardeniers, J.G.E., E-mail: j.g.e.gardeniers@utwente.nl [Mesoscale Chemical Systems, MESA" + Institute for Nanotechnology, University of Twente, P.O. Box 217, 7500 AE Enschede (Netherlands)

2013-05-01

Nickel and other metal nanoparticles are known to be active as catalysts in the synthesis of carbon nanofibers. In this paper we investigate how dewetting and break-up of nickel thin films depends on film thickness, film–substrate interaction and pretreatment conditions. This is evaluated for films evaporated on oxidized silicon and fused silica substrates with or without tantalum coating, which were subsequently exposed to different pretreatment atmospheres (vacuum, nitrogen, air and hydrogen; 1 h, 650 °C). Atomic force microscopy, scanning electron microscopy and energy dispersive X-ray analysis were used to characterize the films. Pretreated Ni films were subjected to a thermal catalytic chemical vapor deposition procedure with brief ethylene exposures (0.5–3 min, 635 °C). It was found that only on the spherical nanoparticles originating from a hydrogen pretreatment of a Ni film with Ta adhesion layer, homogeneously distributed, randomly-oriented, well-attached, and semi-crystalline carbon nanofibers be synthesized. - Highlights: • On the formation of nanoparticles required for carbon nanofiber (CNF) synthesis • Various evaporated thin films on oxidized silicon and fused silica: Ni and Ni/Ta • Pretreatment of nickel-based thin films in vacuum, nitrogen, air and hydrogen • Only on reduced Ni/Ta fast – within 3 min – initiation of CNF nucleation and growth.

Few layer graphene wrapped mixed phase TiO2 nanofiber as a potential electrode material for high performance supercapacitor applications

Science.gov (United States)

Thirugnanam, Lavanya; Sundara, Ramaprabhu

2018-06-01

A combination of favorable composition and optimized anatase/rutile mixed-phase TiO2 (MPTNF)/Hydrogen exfoliated graphene (HEG) composite nanofibers (MPTNF/HEG) and anatase/rutile mixed-phase TiO2/reduced graphene oxide (rGO) composite nanofibers (MPTNF/rGO) have been reported to enhance the electrochemical properties for supercapacitor applications. These composite nanofibers have been synthesized by an efficient route of electrospinning together with the help of easy chemical methods. Both the composites exhibit good charge storage capability with enhanced pseudocapacitance and electric double-layer capacitance (EDLC) as confirmed by cyclic voltammetry studies. MPTNF/HEG composite showed maximum specific capacitance of 210.5 F/g at the current density of 1 A/g, which was mainly due to its availability of the more active sites for ions adsorption on a few layers of graphene wrapped TiO2 nanofiber surface. The synergistic effect of anatase/rutile mixed phase with one dimensional nanostructure and the electronic interaction between TiO2 and few layer graphene provided the subsequent improvement of ion adsorption capacity. Also exhibit excellent electrochemical performance to improve the capacitive properties of TiO2 electrode materials which is required for the development of flexible electrodes in energy storage devices and open up new opportunities for high performance supercapacitors.

Preparation and characterization of kefiran electrospun nanofibers.

Science.gov (United States)

Esnaashari, Seyedeh Sara; Rezaei, Sasan; Mirzaei, Esmaeil; Afshari, Hamed; Rezayat, Seyed Mahdi; Faridi-Majidi, Reza

2014-09-01

In this study, we report the first successful production of kefiran nanofibers through electrospinning process using distilled water as solvent. For this purpose, kefiran was extracted from cultured kefir grains, and homogenous kefiran solutions with different concentrations were prepared and then electrospun to obtain uniform nanofibers. The effect of main process parameters, including applied voltage, tip-to-collector distance, and feeding rate, on diameter and morphology of produced nanofibers, was studied. Scanning electron microscopy (SEM) and attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy were used to characterize electrospun mats. Rheological behavior of the kefiran solution was evaluated via a cone and plate rheometer too. The results exhibited that diameter of kefiran nanofibers increased with increasing polymer concentration, applied voltage, and polymer feeding rate, while tip-to-collector distance did not have significant effect on nanofiber diameter. ATR-FTIR spectra showed that kefiran has maintained its molecular structure during electrospinning process. Flow curves also demonstrated shear thinning behavior for kefiran solutions. Copyright © 2014 Elsevier B.V. All rights reserved.

Cotton nanofibers obtained by different acid conditions

International Nuclear Information System (INIS)

Teixeira, Eliangela de M.; Oliveira, Caue Ribeiro de; Mattoso, Luiz H.C.; Correa, Ana Carolina; Palladin, Priscila

2009-01-01

The thermal stability of cellulose nanofibers is related to their application and especially to polymer processing which temperatures of processing are around 200 deg C. In this work, nanofibers of commercial cotton were obtained by acid hydrolysis employing different acids: sulfuric, hydrochloric and a mixture (2:1; sulfuric acid: hydrochloric acid).The morphology of the nanofibers were characterized by transmission microscopy (TEM), crystallinity by x-ray diffraction (XRD) and thermal stability in air atmosphere by thermogravimetric analysis (TGA). The results indicated a very similar morphology and crystallinity among them. The main differences were relative to aggregation state e and thermal stability. The aggregation state of the suspensions decreases in the order HCl 2 SO 4 :HCl 2 SO 4- . The hydrolysis with a mix of HCl and H 2 SO 4 resulted in cellulose nanofibers with higher thermal stability than those hydrolyzed with H 2 SO 4 . The hydrolysis employed with a mixture of sulphuric and hydrochloric acids also showed a better dispersion than those suspensions of nanofibers obtained by hydrolysis with only HCl. (author)

Physico-chemical/biological properties of tripolyphosphate cross-linked chitosan based nanofibers

Energy Technology Data Exchange (ETDEWEB)

Sarkar, Soumi Dey [School of Medical Science and Technology, Indian Institute of Technology Kharagpur, Kharagpur-721302 (India); Farrugia, Brooke L.; Dargaville, Tim R. [Institute of Health and Biomedical Innovation, Queensland University of Technology, Kelvin Groove, Queensland-4059 (Australia); Dhara, Santanu, E-mail: sdhara@smst.iitkgp.ernet.in [School of Medical Science and Technology, Indian Institute of Technology Kharagpur, Kharagpur-721302 (India)

2013-04-01

In this study, chitosan-PEO blend, prepared in a 15 M acetic acid, was electrospun into nanofibers (∼ 78 nm diameter) with bead free morphology. While investigating physico-chemical parameters of blend solutions, effect of yield stress on chitosan based nanofiber fabrication was clearly evidenced. Architectural stability of nanofiber mat in aqueous medium was achieved by ionotropic cross-linking of chitosan by tripolyphosphate (TPP) ions. The TPP cross-linked nanofiber mat showed swelling up to ∼ 300% in 1 h and ∼ 40% degradation during 30 day study period. 3T3 fibroblast cells showed good attachment, proliferation and viability on TPP treated chitosan based nanofiber mats. The results indicate non-toxic nature of TPP cross-linked chitosan based nanofibers and their potential to be explored as a tissue engineering matrix. - Highlights: ► Chitosan based nanofiber fabrication through electrospinning. ► Roles of solution viscosity and yield stress on spinnability of chitosan evidenced. ► Tripolyphosphate (TPP) cross-linking rendered structural stability to nanofibers. ► TPP cross-linking also improved cellular response on chitosan based nanofibers. ► Thus, chitosan based nanofibers are suitable for tissue engineering application.

Physico-chemical/biological properties of tripolyphosphate cross-linked chitosan based nanofibers

International Nuclear Information System (INIS)

Sarkar, Soumi Dey; Farrugia, Brooke L.; Dargaville, Tim R.; Dhara, Santanu

2013-01-01

In this study, chitosan-PEO blend, prepared in a 15 M acetic acid, was electrospun into nanofibers (∼ 78 nm diameter) with bead free morphology. While investigating physico-chemical parameters of blend solutions, effect of yield stress on chitosan based nanofiber fabrication was clearly evidenced. Architectural stability of nanofiber mat in aqueous medium was achieved by ionotropic cross-linking of chitosan by tripolyphosphate (TPP) ions. The TPP cross-linked nanofiber mat showed swelling up to ∼ 300% in 1 h and ∼ 40% degradation during 30 day study period. 3T3 fibroblast cells showed good attachment, proliferation and viability on TPP treated chitosan based nanofiber mats. The results indicate non-toxic nature of TPP cross-linked chitosan based nanofibers and their potential to be explored as a tissue engineering matrix. - Highlights: ► Chitosan based nanofiber fabrication through electrospinning. ► Roles of solution viscosity and yield stress on spinnability of chitosan evidenced. ► Tripolyphosphate (TPP) cross-linking rendered structural stability to nanofibers. ► TPP cross-linking also improved cellular response on chitosan based nanofibers. ► Thus, chitosan based nanofibers are suitable for tissue engineering application

Obtaining nanofibers from sisal to reinforce nanocomposites biodegradable matrixes

International Nuclear Information System (INIS)

Oliveira, Francieli B. de; Teixeira, Eliangela de M.; Marconcini, Jose M.; Mattoso, Luiz H.C.; Teodoro, Kelcilene B.R.

2009-01-01

Cellulose nanofibers have been extracted by acid hydrolysis from sisal fibers. They are seen a good source material due to availability and low cost. The nanofibers was evaluated by thermal degradation behavior using thermogravimetry (TG), crystallinity by X-ray diffraction and morphological structure was investigated by atomic force microscopy (AFM) experiments. The resulting nanofibers was shown high crystallinity and a network of rodlike cellulose elements. The nanofibers will be incorporated as reinforcement in a biodegradable matrix and evaluated. (author)

Biologically Active Polycaprolactone/Titanium Hybrid Electrospun Nanofibers for Hard Tissue Engineering

DEFF Research Database (Denmark)

Barakat, Nasser A. M.; Sheikh, Faheem A.; Al-Deyab, Salem S.

2011-01-01

In this study, a novel strategy to improve the bioactivity of polycaprolactone nanofibers is proposed. Incorporation of pure titanium nanoparticles into polycaprolactone nanofibers strongly enhances the precipitation of bone-like apatite materials when the doped nanofibers are soaked in a simulat...... nanofiber mats and the successful incorporation of the titanium nanoparticles make the prepared polycaprolactone nanofiber mat a proper candidate for the hard-tissue engineering applications....

Surface functionalization of carbon nanofibers by sol-gel coating of zinc oxide

Energy Technology Data Exchange (ETDEWEB)

Shao Dongfeng [Key Laboratory of Eco-textiles, Ministry of Education, Jiangnan University, Wuxi 214122 (China); Changzhou Textile Garment Institute, Changzhou 213164 (China); Wei Qufu [Key Laboratory of Eco-textiles, Ministry of Education, Jiangnan University, Wuxi 214122 (China)], E-mail: qfwei@jiangnan.edu.cn; Zhang Liwei; Cai Yibing; Jiang Shudong [Key Laboratory of Eco-textiles, Ministry of Education, Jiangnan University, Wuxi 214122 (China)

2008-08-15

In this paper the functional carbon nanofibers were prepared by the carbonization of ZnO coated PAN nanofibers to expand the potential applications of carbon nanofibers. Polyacrylonitrile (PAN) nanofibers were obtained by electrospinning. The electrospun PAN nanofibers were then used as substrates for depositing the functional layer of zinc oxide (ZnO) on the PAN nanofiber surfaces by sol-gel technique. The effects of coating, pre-oxidation and carbonization on the surface morphology and structures of the nanofibers were characterized by X-ray diffraction (XRD), Fourier transform infrared (FTIR) and Scanning electron microscopy (SEM), respectively. The results of SEM showed a significant increase of the size of ZnO nanograins on the surface of nanofibers after the treatments of coating, pre-oxidation and carbonization. The observations by SEM also revealed that ZnO nanoclusters were firmly and clearly distributed on the surface of the carbon nanofibers. FTIR examination also confirmed the deposition of ZnO on the surface of carbon nanofibers. The XRD analysis indicated that the crystal structure of ZnO nanograins on the surface of carbon nanofibers.

Spectroscopic and electrical sensing mechanism in oxidant-mediated polypyrrole nanofibers/nanoparticles for ammonia gas

International Nuclear Information System (INIS)

Ishpal; Kaur, Amarjeet

2013-01-01

Ammonia gas sensing mechanism in oxidant-mediated polypyrrole (PPy) nanofibers/nanoparticles has been studied through spectroscopic and electrical investigations. PPy nanofibers/nanoparticles have been synthesized by chemical oxidation method in the presence of various oxidizing agents such as ammonium persulfate (APS), potassium persulfate (PPS), vanadium pentoxide (V 2 O 5 ), and iron chloride (FeCl 3 ). Scanning electron microscopy study revealed that PPy nanofibers of about 63, 71 and 79 nm diameters were formed in the presence of APS, PPS, V 2 O 5 , respectively, while PPy nanoparticles of about 100–110 nm size were obtained in the presence of FeCl 3 as an oxidant. The structural investigations and confirmation of synthesis of PPy were established through Fourier transform infrared and Raman spectroscopy. The gas sensing behavior of the prepared PPy samples is investigated by measuring the electrical resistance in ammonia environment. The observed gas sensing response (ΔR/Rx100) at 100 ppm level of ammonia is ∼4.5 and 18 % for the samples prepared with oxidizing agents FeCl 3 and APS, respectively, and by changing the ammonia level from 50 to 300 ppm, the sensing response varies from ∼4.5 to 11 % and ∼10 to 39 %, respectively. Out of all four samples, the PPy nanofibers prepared in the presence of APS have shown the best sensing response. The mechanism of gas sensing response of the PPy samples has been investigated through Raman spectroscopy study. The decrease of charge carrier concentration through reduction of polymeric chains has been recognized through Raman spectroscopic measurements recorded in ammonia environment.

Recognition of lysozyme using surface imprinted bacterial cellulose nanofibers.

Science.gov (United States)

Saylan, Yeşeren; Tamahkar, Emel; Denizli, Adil

2017-11-01

Here, we developed the lysozyme imprinted bacterial cellulose (Lyz-MIP/BC) nanofibers via the surface imprinting strategy that was designed to recognize lysozyme. This study includes the molecular imprinting method onto the surface of bacterial cellulose nanofibers in the presence of lysozyme by metal ion coordination, as well as further characterizations methods FTIR, SEM and contact angle measurements. The maximum lysozyme adsorption capacity of Lyz-MIP/BC nanofibers was found to be 71 mg/g. The Lyz-MIP/BC nanofibers showed high selectivity for lysozyme towards bovine serum albumin and cytochrome c. Overall, the Lyz-MIP/BC nanofibers hold great potential for lysozyme recognition due to the high binding capacity, significant selectivity and excellent reusability.

Coaxial nanofibers containing TiO2 in the shell for water treatment applications

Science.gov (United States)

Kizildag, N.; Geltmeyer, J.; Ucar, N.; De Buysser, K.; De Clerck, K.

2017-10-01

In recent years, the basic electrospinning setup has undergone many modifications carried out to enhance the quality and improve the functionality of the resulting nanofibers. Being one of these modifications, coaxial electrospinning has attracted great attention. It enables to use different materials in nanofiber production and produce multi-layered and functional nanofibers in one step. In this study, TiO2 has been added to the shell layer of coaxial nanofibers to develop functional nanofibers which may be used in water treatment applications. The coaxial nanofibers containing TiO2 in the shell layer are compared to uniaxial nanofibers containing TiO2 in bulk fiber structure, regarding their morphology and photocatalytic activity. Uniform uniaxial and coaxial nanofibers with TiO2 were obtained. The average nanofiber diameter of coaxial nanofibers were higher. Coaxial nanofibers, which contained lower amount of TiO2, displayed similar performance to uniaxial nanofibers with TiO2 in terms of photocatalytic degradation ability against isoproturon.

The effect of thai glutinous rice starch on the synthesis of lead zirconate (PbZrO3) nanofibers via the electrospinning method.

Science.gov (United States)

Nawanil, Chanisa; Vittayakorn, Wanwilai; Muanghua, Rangson; Niemcharoen, Surasak; Prachayawarakorn, Jutarat; Vittayakorn, Naratip

2013-05-01

This study synthesized blended lead zirconate (PbZrO3;PZ)/poly(ethylene oxide)(PEO)/Glutinous rice starch (GRS) nanofibers by the electrospinning method. A number of parameters such as the ratio between PEO and GRS and calcination temperature have been studied. The as-spun PZ/PEO/GRS composite and PZ fibers were characterized by TG-DTA, X-ray diffraction, FT-IR and SEM, respectively. SEM results showed that smooth and continuous fibers were obtained at the volume ratio of 10:2:1, PZ/PEO/GRS. After calcination of the as-spun PZ/PEO/GRS composite nanofibers at 650 degrees C for 4 h, PZ nanofibers with perovskite structure were obtained successfully. The fibers had a uniform and smooth surface without grain boundaries. However, when the calcination temperature increased to 750 degrees C and 850 degrees C, the fiber represented a necklace-like structure with grain boundaries arranged by grain to grain unit cell clusters.

Temperature-responsive PLLA/PNIPAM nanofibers for switchable release

Energy Technology Data Exchange (ETDEWEB)

Elashnikov, Roman; Slepička, Petr [Department of Solid State Engineering, University of Chemistry and Technology, Prague 166 28 (Czech Republic); Rimpelova, Silvie; Ulbrich, Pavel [Department of Biochemistry and Microbiology, University of Chemistry and Technology, 16628 Prague (Czech Republic); Švorčík, Vaclav [Department of Solid State Engineering, University of Chemistry and Technology, Prague 166 28 (Czech Republic); Lyutakov, Oleksiy, E-mail: lyutakoo@vscht.cz [Department of Solid State Engineering, University of Chemistry and Technology, Prague 166 28 (Czech Republic)

2017-03-01

Smart antimicrobial materials with on-demand drug release are highly desired for biomedical applications. Herein, we report about temperature-responsive poly(N-isopropylacrylamide) (PNIPAM) nanospheres doped with crystal violet (CV) and incorporated into the poly-L-lactide (PLLA) nanofibers. The nanofibers were prepared by electrospinning, using different initial polymers ratios. The morphology of the nanofibers and polymers distribution in the nanofibers were characterized by scanning electron microscopy (SEM) and atomic force microscopy (AFM). The interaction between PNIPAM and PLLA in the nanofibers was studied by Fourier transform infrared spectroscopy (FTIR) and its effect on the PNIPAM phase transition was also investigated. It was shown that by the changing of the environmental temperature across the lower critical solution temperature (LCST) of PNIPAM, the switchable wettability and controlled CV release can be achieved. The temperature-dependent release kinetics of CV from polymer nanofibers was investigated by ultraviolet-visible spectroscopy (UV–Vis). The temperature-responsive release of antibacterial CV was also tested for triggering of antibacterial activity, which was examined on Staphylococcus epidermidis (S. epidermidis) and Escherichia coli (E. coli). Thus, the proposed material is promising value for controllable drug-release.

Synthesis of Keratin-based Nanofiber for Biomedical Engineering.

Science.gov (United States)

Thompson, Zanshe S; Rijal, Nava P; Jarvis, David; Edwards, Angela; Bhattarai, Narayan

2016-02-07

Electrospinning, due to its versatility and potential for applications in various fields, is being frequently used to fabricate nanofibers. Production of these porous nanofibers is of great interest due to their unique physiochemical properties. Here we elaborate on the fabrication of keratin containing poly (ε-caprolactone) (PCL) nanofibers (i.e., PCL/keratin composite fiber). Water soluble keratin was first extracted from human hair and mixed with PCL in different ratios. The blended solution of PCL/keratin was transformed into nanofibrous membranes using a laboratory designed electrospinning set up. Fiber morphology and mechanical properties of the obtained nanofiber were observed and measured using scanning electron microscopy and tensile tester. Furthermore, degradability and chemical properties of the nanofiber were studied by FTIR. SEM images showed uniform surface morphology for PCL/keratin fibers of different compositions. These PCL/keratin fibers also showed excellent mechanical properties such as Young's modulus and failure point. Fibroblast cells were able to attach and proliferate thus proving good cell viability. Based on the characteristics discussed above, we can strongly argue that the blended nanofibers of natural and synthetic polymers can represent an excellent development of composite materials that can be used for different biomedical applications.

Nanocontainers in and onto Nanofibers.

Science.gov (United States)

Jiang, Shuai; Lv, Li-Ping; Landfester, Katharina; Crespy, Daniel

2016-05-17

Hierarchical structure is a key feature explaining the superior properties of many materials in nature. Fibers usually serve in textiles, for structural reinforcement, or as support for other materials, whereas spherical micro- and nanoobjects can be either highly functional or also used as fillers to reinforce structure materials. Combining nanocontainers with fibers in one single object has been used to increase the functionality of fibers, for example, antibacterial and thermoregulation, when the advantageous properties given by the encapsulated materials inside the containers are transferred to the fibers. Herein we focus our discussion on how the hierarchical structure composed of nanocontainers in nanofibers yields materials displaying advantages of both types of materials and sometimes synergetical effects. Such materials can be produced by first carefully designing nanocontainers with defined morphology and chemistry and subsequently electrospinning them to fabricate nanofibers. This method, called colloid-electrospinning, allows for marrying the properties of nanocontainers and nanofibers. The obtained fibers could be successfully applied in different fields such as catalysis, optics, energy conversion and production, and biomedicine. The miniemulsion process is a convenient approach for the encapsulation of hydrophobic or hydrophilic payloads in nanocontainers. These nanocontainers can be embedded in fibers by the colloid-electrospinning technique. The combination of nanocontainers with nanofibers by colloid-electrospinning has several advantages. (1) The fiber matrix serves as support for the embedded nanocontainers. For example, through combining catalysts nanoparticles with fiber networks, the catalysts can be easily separated from the reaction media and handled visually. This combination is beneficial for the reuse of the catalyst and the purification of products. (2) Electrospun nanofibers containing nanocontainers offer the active agents inside the

General strategy for fabricating thoroughly mesoporous nanofibers

KAUST Repository

Hou, Huilin; Wang, Lin; Gao, Fengmei; Wei, Guodong; Tang, Bin; Yang, Weiyou; Wu, Tao

2014-01-01

mesoporous nanofibers with high purity and uniformity. Here, we report a general, simple and cost-effective strategy, namely, foaming-assisted electrospinning, for producing mesoporous nanofibers with high purity and enhanced specific surface areas. As a

Single flexible nanofiber to simultaneously realize electricity-magnetism bifunctionality

International Nuclear Information System (INIS)

Yang, Ming; Sheng, Shujuan; Ma, Qianli; Lv, Nan; Yu, Wensheng; Wang, Jinxian; Dong, Xiangting; Liu, Guixia

2016-01-01

In order to develop new-typed multifunctional composite nanofibers, PANI/Fe 3 O 4 /PVP flexible bifunctional composite nanofibers with simultaneous electrical conduction and magnetism have been successfully fabricated via a facile electrospinning technology. Polyvinyl pyrrolidone (PVP) is used as a matrix to construct composite nanofibers containing different amounts of polyaniline (PANI) and Fe 3 O 4 nanoparticles (NPs). The bifunctional composite nanofibers simultaneously possess excellent electrical conductivity and magnetic properties. The electrical conductivity reaches up to the order of 10 -3 S·cm -1 . The electrical conductivity and saturation magnetization of the composite nanofibers can be respectively tuned by adding various amounts of PANI and Fe 3 O 4 NPs. The obtained electricity-magnetism bifunctional composite nanofibers are expected to possess many potential applications in areas such as electromagnetic interference shielding, special coating, microwave absorption, molecular electronics and future nanomechanics. More importantly, the design concept and construct technique are of universal significance to fabricate other bifunctional one-dimensional nanostructures. (author)

Evaluation of protein adsorption onto a polyurethane nanofiber surface having different segment distributions

Energy Technology Data Exchange (ETDEWEB)

Morita, Yuko; Koizumi, Gaku [Frontier Fiber Technology and Science, Graduate School of Engineering, University of Fukui (Japan); Sakamoto, Hiroaki, E-mail: hi-saka@u-fukui.ac.jp [Tenure-Track Program for Innovative Research, University of Fukui (Japan); Suye, Shin-ichiro [Frontier Fiber Technology and Science, Graduate School of Engineering, University of Fukui (Japan)

2017-02-01

Electrospinning is well known to be an effective method for fabricating polymeric nanofibers with a diameter of several hundred nanometers. Recently, the molecular-level orientation within nanofibers has attracted particular attention. Previously, we used atomic force microscopy to visualize the phase separation between soft and hard segments of a polyurethane (PU) nanofiber surface prepared by electrospinning. The unstretched PU nanofibers exhibited irregularly distributed hard segments, whereas hard segments of stretched nanofibers prepared with a high-speed collector exhibited periodic structures along the long-axis direction. PU was originally used to inhibit protein adsorption, but because the surface segment distribution was changed in the stretched nanofiber, here, we hypothesized that the protein adsorption property on the stretched nanofiber might be affected. We investigated protein adsorption onto PU nanofibers to elucidate the effects of segment distribution on the surface properties of PU nanofibers. The amount of adsorbed protein on stretched PU nanofibers was increased compared with that of unstretched nanofibers. These results indicate that the hard segment alignment on stretched PU nanofibers mediated protein adsorption. It is therefore expected that the amount of protein adsorption can be controlled by rotation of the collector. - Highlights: • The hard segments of stretched PU nanofibers exhibit periodic structures. • The adsorbed protein on stretched PU nanofibers was increased compared with PU film. • The hard segment alignment on stretched PU nanofibers mediated protein adsorption.

Nanofiber Filters Eliminate Contaminants

Science.gov (United States)

2009-01-01

With support from Phase I and II SBIR funding from Johnson Space Center, Argonide Corporation of Sanford, Florida tested and developed its proprietary nanofiber water filter media. Capable of removing more than 99.99 percent of dangerous particles like bacteria, viruses, and parasites, the media was incorporated into the company's commercial NanoCeram water filter, an inductee into the Space Foundation's Space Technology Hall of Fame. In addition to its drinking water filters, Argonide now produces large-scale nanofiber filters used as part of the reverse osmosis process for industrial water purification.

Electrospun nanofibers: New generation materials for advanced applications

Energy Technology Data Exchange (ETDEWEB)

Thenmozhi, S. [Inorganic & Nanomaterials Research Laboratory, Department of Chemistry, Bharathiar University, Coimbatore 641 046 (India); DRDO-BU CLS, Bharathiar University Campus, Coimbatore 641 046 (India); Dharmaraj, N., E-mail: dharmaraj@buc.edu.in [Inorganic & Nanomaterials Research Laboratory, Department of Chemistry, Bharathiar University, Coimbatore 641 046 (India); Kadirvelu, K. [DRDO-BU CLS, Bharathiar University Campus, Coimbatore 641 046 (India); Kim, Hak Yong [Department of Textile Engineering, Chonbuk National University, Chonju 561-756 (Korea, Republic of)

2017-03-15

Highlights: • A review covering important aspects of electrospinning technique is presented. • Applications of nanofibers in various fields are reviewed. • Possibility to up-scale electrospinning technique to industry also included. - Abstract: Electrospinning (E-spin) is a unique technique to fabricate polymeric as well as metal oxide nanofibers. Research on electrospun nanofibers is a very active field in material science owing to their novel applications in diverse domains. The main focus of this review is to provide an insight into E-spin technique by understanding the working principle, influencing parameters and applications of nanofibers in different walks of life. Several hundreds of papers are published on the preparation, modification and applications of nanofibers produced by E-spin technique in the areas like sensor development, decontamination, energy storage, biomedical and catalysis etc. Details on the industrial scale development of E-spin technique, current scenario and future developments are also covered in this review.

PVDF nanofibers with silver nanoparticles and silver/titanium dioxide for antimicrobial applications;Eletrofiacao de nanofibras de PVDF com nanoparticulas de prata e de prata/dioxido de titanio para aplicacoes antimicrobiais

Energy Technology Data Exchange (ETDEWEB)

Costa, Ligia M.M.; Olyveira, Gabriel M. de, E-mail: gmolyveira@yahoo.com.b, E-mail: ligialmmc@hotmail.co [Universidade Federal de Sao Carlos (PPGCEM/UFScar), SP (Brazil). Programa de Pos Graduacao em Ciencia e Engenharia de Materiais; Gregorio Filho, Rinaldo; Pessan, Luiz A., E-mail: pessan@ufscar.b, E-mail: gregorio@ufscar.b [Universidade Federal de Sao Carlos (UFScar), SP (Brazil)

2009-07-01

PVDF nanofibers with and without nanoparticles were produced by the method of electro spinning using dimethylformamide (DMF). Silver nitrate nanoparticles (0,5 and 2 wt %) and silver/titanium dioxide nanoparticles obtained by the reduction method (2 wt %) were synthesized and added to the PVDF solution to prepared nanofibers. The processes of electrospinning and film preparation using PVDF with the nanoparticles were compared. Silver/titanium dioxide nanoparticles were characterized with X-ray diffraction (XRD), Scanning electron microscopy (SEM) with EDX and x-ray photoelectron spectroscopy (XPS) to show silver/titanium dioxide nanoparticles. Nanofibers mats were characterized with SEM to study the effects of the addition of the nanoparticles on the morphology behavior and spectroscopy by Fourier transform infrared (FTIR) to analyze the crystalline phase of PVDF films. (author)

High performance co-polyimide nanofiber reinforced composites

NARCIS (Netherlands)

Yao, Jian; Li, Guang; Bastiaansen, Cees; Peijs, Ton

2015-01-01

Electrospun co-polyimide BPDA (3, 3′, 4, 4′-Biphenyltetracarboxylic dianhydride)/PDA (p-Phenylenediamine)/ODA (4, 4′-oxydianiline) nanofiber reinforced flexible composites were manufactured by impregnating these high performance nanofibers with styrene-butadiene-styrene (SBS) triblock copolymer

The Electrospun Ceramic Hollow Nanofibers

Directory of Open Access Journals (Sweden)

Shahin Homaeigohar

2017-11-01

Full Text Available Hollow nanofibers are largely gaining interest from the scientific community for diverse applications in the fields of sensing, energy, health, and environment. The main reasons are: their extensive surface area that increases the possibilities of engineering, their larger accessible active area, their porosity, and their sensitivity. In particular, semiconductor ceramic hollow nanofibers show greater space charge modulation depth, higher electronic transport properties, and shorter ion or electron diffusion length (e.g., for an enhanced charging–discharging rate. In this review, we discuss and introduce the latest developments of ceramic hollow nanofiber materials in terms of synthesis approaches. Particularly, electrospinning derivatives will be highlighted. The electrospun ceramic hollow nanofibers will be reviewed with respect to their most widely studied components, i.e., metal oxides. These nanostructures have been mainly suggested for energy and environmental remediation. Despite the various advantages of such one dimensional (1D nanostructures, their fabrication strategies need to be improved to increase their practical use. The domain of nanofabrication is still advancing, and its predictable shortcomings and bottlenecks must be identified and addressed. Inconsistency of the hollow nanostructure with regard to their composition and dimensions could be one of such challenges. Moreover, their poor scalability hinders their wide applicability for commercialization and industrial use.

Preparing photochromic nanofibers and animal cells using a photochromic compound of 1′,3′,3′-trimethyl-6-nitrospiro (2H-1-benzopyran-2,2′-indoline)

DEFF Research Database (Denmark)

Li, Xiaoqiang; Lin, Lin; Kanjwal, Muzafar Ahmed

2012-01-01

In this work, the photochromic compound 1′,3′,3′-trimethyl-6-nitrospiro (2H-1-benzopyran-2,2′-indoline) (NOSP) was synthesized by a two step process. The photochromic properties of NOSP were investigated by ultraviolet–visible (UV–Vis) spectrophotometry. The results showed that NOSP was very...... electrospinning were characterized by water contact angle measurements, ultraviolet–visible (UV–Vis) spectrophotometry and fluorescence microscopy. Morphology of photochromic PIEC was observed by fluorescence microscopy after being irradiated. It was shown that nanofibers from electrospun polymers and NOSP...... sensitive to UV irradiation with absorption peaks at about 336nm and 567nm. Our hypothesis was that both photochromic nanofibers and photochromic living animal cells could be obtained by combining them with NOSP. To test the hypothesis, photochromic nanofibers were fabricated by electrospinning from various...

ECM Decorated Electrospun Nanofiber for Improving Bone Tissue Regeneration

Directory of Open Access Journals (Sweden)

Yong Fu

2018-03-01

Full Text Available Optimization of nanofiber surface properties can lead to enhanced tissue regeneration outcomes in the context of bone tissue engineering. Herein, we developed a facile strategy to decorate elctrospun nanofibers using extracellular matrix (ECM in order to improve their performance for bone tissue engineering. Electrospun PLLA nanofibers (PLLA NF were seeded with MC3T3-E1 cells and allowed to grow for two weeks in order to harvest a layer of ECM on nanofiber surface. After decellularization, we found that ECM was successfully preserved on nanofiber surface while maintaining the nanostructure of electrospun fibers. ECM decorated on PLLA NF is biologically active, as evidenced by its ability to enhance mouse bone marrow stromal cells (mBMSCs adhesion, support cell proliferation and promote early stage osteogenic differentiation of mBMSCs. Compared to PLLA NF without ECM, mBMSCs grown on ECM/PLLA NF exhibited a healthier morphology, faster proliferation profile, and more robust osteogenic differentiation. Therefore, our study suggests that ECM decoration on electrospun nanofibers could serve as an efficient approach to improving their performance for bone tissue engineering.

Single flexible nanofiber to simultaneously realize electricity-magnetism bifunctionality

Energy Technology Data Exchange (ETDEWEB)

Yang, Ming; Sheng, Shujuan; Ma, Qianli; Lv, Nan; Yu, Wensheng; Wang, Jinxian; Dong, Xiangting; Liu, Guixia, E-mail: wenshengyu2009@sina.com, E-mail: dongxiangting888@163.com [Key Laboratory of Applied Chemistry and Nanotechnology at Universities of Jilin Province, Changchun University of Science and Technology, Changchun (China)

2016-03-15

In order to develop new-typed multifunctional composite nanofibers, PANI/Fe{sub 3}O{sub 4}/PVP flexible bifunctional composite nanofibers with simultaneous electrical conduction and magnetism have been successfully fabricated via a facile electrospinning technology. Polyvinyl pyrrolidone (PVP) is used as a matrix to construct composite nanofibers containing different amounts of polyaniline (PANI) and Fe{sub 3}O{sub 4} nanoparticles (NPs). The bifunctional composite nanofibers simultaneously possess excellent electrical conductivity and magnetic properties. The electrical conductivity reaches up to the order of 10{sup -3} S·cm{sup -1}. The electrical conductivity and saturation magnetization of the composite nanofibers can be respectively tuned by adding various amounts of PANI and Fe{sub 3}O{sub 4} NPs. The obtained electricity-magnetism bifunctional composite nanofibers are expected to possess many potential applications in areas such as electromagnetic interference shielding, special coating, microwave absorption, molecular electronics and future nanomechanics. More importantly, the design concept and construct technique are of universal significance to fabricate other bifunctional one-dimensional nanostructures. (author)

Syntheses and Self-assembling Behaviors of Pentagonal Conjugates of Tryptophane Zipper-Forming Peptide

Directory of Open Access Journals (Sweden)

Nobuo Kimizuka

2011-08-01

Full Text Available Pentagonal conjugates of tryptophane zipper-forming peptide (CKTWTWTE with a pentaazacyclopentadecane core (Pentagonal-Gly-Trpzip and Pentagonal-Ala-Trpzip were synthesized and their self-assembling behaviors were investigated in water. Pentagonal-Gly-Trpzip self-assembled into nanofibers with the width of about 5 nm in neutral water (pH 7 via formation of tryptophane zipper, which irreversibly converted to nanoribbons by heating. In contrast, Pentagonal-Ala-Trpzip formed irregular aggregates in water.

Superhydrophilicity of novel anodic alumina nanofibers films and their formation mechanism

Science.gov (United States)

Peng, Rong; Yang, Wulin; Fu, Licai; Zhu, Jiajun; Li, Deyi; Zhou, Lingping

2017-06-01

A novel anodic alumina nanofibers structure, which is different from the traditional porous anodic structure, has been quickly fabricated via anodizing in a new electrolyte, pyrophosphoric acid. The effects of the solution concentration and the anodizing time on the formation of the anodic alumina nanofibers were analyzed. The results show that the nanostructure of anodic alumina can change to the nanofiber oxide from the porous oxide by increasing the solution concentration. Prolonging the anodizing time is beneficial to obtain alumina nanofibers at high solution concentration. Growth behavior of the alumina nanofibers was also discussed by scanning electron microscopy observations. Owing to the unique hexagonal structure of anodic alumina as well as the preferential chemical dissolution between the porous anodic alumina and the anodic alumina nanotips, the slightly soluble anodic alumina nanotips could form novel alumina nanofibers during anodizing. The results show that the nanofibers-covered aluminum surface exhibits superhydrophilic property, with a near-zero water contact angle. Such alumina nanofibers with superhydrophilic property could be used for various potential applications.

Free-Standing Porous Carbon Nanofiber Networks from Electrospinning Polyimide for Supercapacitors

Directory of Open Access Journals (Sweden)

Bo Wang

2016-01-01

Full Text Available Free-standing porous carbon nanofiber networks (CFNs were synthesized by electrospinning method and carbonization procedure. We study the implementation of porous CFNs as supercapacitor electrodes and electrochemical measurements demonstrated that porous CFNs exhibit a specific capacitance (205 F/g at the scan rate of 5 mV/s with high flexibility and good rate capability performance (more than 70% of its initial capacitance from 5 mV/s to 200 mV/s. Furthermore, porous CFNs exhibited an excellent cycling stability (just 12% capacitance loss after 10,000 cycles. These results suggest that porous CFNs are very promising candidates as flexible supercapacitor electrodes.

Thermal and Electrical Characterization of the Carbon Nanofibers Based Cement Composites

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Agnieszka ŚLOSARCZYK

2017-08-01

Full Text Available The paper describes the influence of chemical modification of vapor grown carbon nanofibers (VGCnFs on the thermal and electrical properties of the cement composites. The surface modification of nanofibers was performed by means of ozone and nitric acid treatments. It was shown that the oxidized carbon nanofibers surface plays an important role in shaping the mechanical and especially electrical properties of cement composite. For cement matrix modified with carbon nanofibers subjected to oxidized treatment, the slightly increase of cement paste resistivity was observed. It confirms the better adhesion of carbon nanofibers to cement paste. However, independently of carbon nanofibers modification, the occurrence of VGCnFs in cement paste increased the electrical conductivity of the composite in comparison to the cement paste without fibers. The obtained values of electrical resistivity were comparable with values of cement composites modified with 4 mm long carbon fibers. Moreover, it was shown that the chemical modification of carbon nanofibers surface does not influence on the thermal properties of cement composites. In case of cement paste with unmodified and modified carbon nanofibers, the Seebeck voltage was proportional to the temperature difference and was independent of the oxidation degree of carbon nanofibers.DOI: http://dx.doi.org/10.5755/j01.ms.23.2.14993

Fabrication and Characterization of Cellulose Acetate/Montmorillonite Composite Nanofibers by Electrospinning

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Se Wook Kim

2015-01-01

Full Text Available Nanofibers composed of cellulose acetate (CA and montmorillonite (MMT were prepared by electrospinning method. MMT was first dispersed in water and mixed with an acetic acid solution of CA. The viscosity and conductivity of the CA/MMT solutions with different MMT contents were measured to compare with those of the CA solution. The CA/MMT solutions were electrospun to fabricate the CA/MMT composite nanofibers. The morphology, thermal stability, and crystalline and mechanical properties of the composite nanofibers were characterized by scanning electron microscopy (SEM, transmission electron microscopy (TEM, energy dispersive X-ray spectroscopy (EDX, thermogravimetric analysis (TGA, X-ray diffraction (XRD, and tensile test. The average diameters of the CA/MMT composite nanofibers obtained by electrospinning 18 wt% CA/MMT solutions in a mixed acetic acid/water (75/25, w/w solvent ranged from 150~350 nm. The nanofiber diameter decreased with increasing MMT content. TEM indicated the coexistence of CA nanofibers. The CA/MMT composite nanofibers showed improved tensile strength compared to the CA nanofiber due to the physical protective barriers of the silicate clay layers. MMT could be incorporated into the CA nanofibers resulting in about 400% improvement in tensile strength for the CA sample containing 5 wt% MMT.

Structural characteristics of carbon nanofibers for on-chip interconnect applications

International Nuclear Information System (INIS)

Ominami, Yusuke; Ngo, Quoc; Austin, Alexander J.; Yoong, Hans; Yang, Cary Y.; Cassell, Alan M.; Cruden, Brett A.; Li Jun; Meyyappan, M.

2005-01-01

In this letter, we compare the structures of plasma-enhanced chemical vapor deposition of Ni-catalyzed and Pd-catalyzed carbon nanofibers (CNFs) synthesized for on-chip interconnect applications with scanning transmission electron microscopy (STEM). The Ni-catalyzed CNF has a conventional fiberlike structure and many graphitic layers that are almost parallel to the substrate at the CNF base. In contrast, the Pd-catalyzed CNF has a multiwall nanotubelike structure on the sidewall spanning the entire CNF. The microstructure observed in the Pd-catalyzed fibers at the CNF-metal interface has the potential to lower contact resistance significantly, as our electrical measurements using current-sensing atomic force microscopy indicate. A structural model is presented based on STEM image analysis

Biocompatible Electroactive Tetra(aniline)-Conjugated Peptide Nanofibers for Neural Differentiation.

Science.gov (United States)

Arioz, Idil; Erol, Ozlem; Bakan, Gokhan; Dikecoglu, F Begum; Topal, Ahmet E; Urel, Mustafa; Dana, Aykutlu; Tekinay, Ayse B; Guler, Mustafa O

2018-01-10

Peripheral nerve injuries cause devastating problems for the quality of patients' lives, and regeneration following damage to the peripheral nervous system is limited depending on the degree of the damage. Use of nanobiomaterials can provide therapeutic approaches for the treatment of peripheral nerve injuries. Electroactive biomaterials, in particular, can provide a promising cure for the regeneration of nerve defects. Here, a supramolecular electroactive nanosystem with tetra(aniline) (TA)-containing peptide nanofibers was developed and utilized for nerve regeneration. Self-assembled TA-conjugated peptide nanofibers demonstrated electroactive behavior. The electroactive self-assembled peptide nanofibers formed a well-defined three-dimensional nanofiber network mimicking the extracellular matrix of the neuronal cells. Neurite outgrowth was improved on the electroactive TA nanofiber gels. The neural differentiation of PC-12 cells was more advanced on electroactive peptide nanofiber gels, and these biomaterials are promising for further use in therapeutic neural regeneration applications.

Electrochromic device based on electrospun WO{sub 3} nanofibers

Energy Technology Data Exchange (ETDEWEB)

Dulgerbaki, Cigdem; Maslakci, Neslihan Nohut; Komur, Ali Ihsan; Oksuz, Aysegul Uygun, E-mail: ayseguluygun@sdu.edu.tr

2015-12-15

Highlights: • WO{sub 3} electrochromic nanofibers were prepared by electrospinning technique. • WO{sub 3} nanofibers switched reversibly from transparent to blue color. • Electrochromic device was assembled using ionic liquid based gel electrolyte. • Significant optical modulation and excellent cycling stability were achieved for ECD. - Abstract: The tungsten oxide (WO{sub 3}) nanofibers were grown directly onto an ITO-coated glass via an electrospinning method for electrochromic applications. The electrochromic properties of WO{sub 3} nanofibers were investigated in the presence of different electrolytes including a series of ionic liquids and classic LiClO{sub 4}-PC system. A significant optical modulation of 20.82% at 760 nm, reversible coloration with efficiency of 64.58 cm{sup 2}/C and excellent cycling stability were achieved for the nanofiber electrochromic device (ECD) with ionic liquid based gel electrolyte.

Nanofibers made of globular proteins.

Science.gov (United States)

Dror, Yael; Ziv, Tamar; Makarov, Vadim; Wolf, Hila; Admon, Arie; Zussman, Eyal

2008-10-01

Strong nanofibers composed entirely of a model globular protein, namely, bovine serum albumin (BSA), were produced by electrospinning directly from a BSA solution without the use of chemical cross-linkers. Control of the spinnability and the mechanical properties of the produced nanofibers was achieved by manipulating the protein conformation, protein aggregation, and intra/intermolecular disulfide bonds exchange. In this manner, a low-viscosity globular protein solution could be modified into a polymer-like spinnable solution and easily spun into fibers whose mechanical properties were as good as those of natural fibers made of fibrous protein. We demonstrate here that newly formed disulfide bonds (intra/intermolecular) have a dominant role in both the formation of the nanofibers and in providing them with superior mechanical properties. Our approach to engineer proteins into biocompatible fibrous structures may be used in a wide range of biomedical applications such as suturing, wound dressing, and wound closure.

Electrical Impedance Measurements of PZT Nanofiber Sensors

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Richard Galos

2017-01-01

Full Text Available Electrical impedance measurements of PZT nanofiber sensors were performed using a variety of methods over a frequency spectrum ranging from DC to 1.8 GHz. The nanofibers formed by electrospinning with diameters ranging from 10 to 150 nm were collected and integrated into sensors using microfabrication techniques. Special matching circuits with ultrahigh input impedance were fabricated to produce low noise, measurable sensor outputs. Material properties including resistivity and dielectric constant are derived from the impedance measurements. The resulting material properties are also compared with those of individual nanofibers being tested using conductive AFM and Scanning Conductive Microscopy.

Ammonia Sensing Behaviors of TiO2-PANI/PA6 Composite Nanofibers

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Fenglin Huang

2012-12-01

Full Text Available Titanium dioxide-polyaniline/polyamide 6 (TiO2-PANI/PA6 composite nanofibers were prepared by in situ polymerization of aniline in the presence of PA6 nanofibers and a sputtering-deposition process with a high purity titanium sputtering target. TiO2-PANI/PA6 composite nanofibers and PANI/PA6 composite nanofibers were fabricated for ammonia gas sensing. The ammonia sensing behaviors of the sensors were examined at room temperature. All the results indicated that the ammonia sensing property of TiO2-PANI/PA6 composite nanofibers was superior to that of PANI/PA6 composite nanofibers. TiO2-PANI/PA6 composite nanofibers had good selectivity to ammonia. It was also found that the content of TiO2 had a great influence on both the morphology and the sensing property of TiO2-PANI/PA6 composite nanofibers.

Single flexible nanofiber to achieve simultaneous photoluminescence-electrical conductivity bifunctionality.

Science.gov (United States)

Sheng, Shujuan; Ma, Qianli; Dong, Xiangting; Lv, Nan; Wang, Jinxian; Yu, Wensheng; Liu, Guixia

2015-02-01

In order to develop new-type multifunctional composite nanofibers, Eu(BA)3 phen/PANI/PVP bifunctional composite nanofibers with simultaneous photoluminescence and electrical conductivity have been successfully fabricated via electrospinning technology. Polyvinyl pyrrolidone (PVP) is used as a matrix to construct composite nanofibers containing different amounts of Eu(BA)3 phen and polyaniline (PANI). X-Ray diffractometry (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), vibrating sample magnetometry (VSM), fluorescence spectroscopy and a Hall effect measurement system are used to characterize the morphology and properties of the composite nanofibers. The results indicate that the bifunctional composite nanofibers simultaneously possess excellent photoluminescence and electrical conductivity. Fluorescence emission peaks of Eu(3+) ions are observed in the Eu(BA)3 phen/PANI/PVP photoluminescence-electrical conductivity bifunctional composite nanofibers. The electrical conductivity reaches up to the order of 10(-3)  S/cm. The luminescent intensity and electrical conductivity of the composite nanofibers can be tuned by adjusting the amounts of Eu(BA)3 phen and PANI. The obtained photoluminescence-electrical conductivity bifunctional composite nanofibers are expected to possess many potential applications in areas such as microwave absorption, molecular electronics, biomedicine and future nanomechanics. More importantly, the design concept and construction technique are of universal significance to fabricate other bifunctional one-dimensional naonomaterials. Copyright © 2014 John Wiley & Sons, Ltd.

Electrospun MOF nanofibers as hydrogen storage media

CSIR Research Space (South Africa)

Ren, Jianwei

2015-06-01

Full Text Available showed that the incorporation of vacuum degassing was able to create visible porosity in and/or on the PAN nanofibers and the MOF nanocrystals inside the polymeric nanofibers were fully accessible by N2 and H2 gases. With 20 wt.% loading of MOF...

Cellulose nanofiber extraction from grass by a modified kitchen blender

Science.gov (United States)

Nakagaito, Antonio Norio; Ikenaga, Koh; Takagi, Hitoshi

2015-03-01

Cellulose nanofibers have been used to reinforce polymers, delivering composites with strength that in some cases can be superior to that of engineering plastics. The extraction of nanofibers from plant fibers can be achieved through specialized equipment that demands high energy input, despite delivering extremely low yields. The high extraction cost confines the use of cellulose nanofibers to the laboratory and not for industrial applications. This study aims to extract nanofibers from grass by using a kitchen blender. Earlier studies have demonstrated that paper sheets made of blender-extracted nanofibers (after 5 min to 10 min of blending) have strengths on par with paper sheets made from commercially available cellulose nanofibers. By optimizing the design of the blender bottle, nanofibrillation can be achieved in shorter treatment times, reducing the energy consumption (in the present case, to half) and the overall extraction cost. The raw materials used can be extended to the residue straw of agricultural crops, as an alternative to the usual pulp fibers obtained from wood.

Development of green nanocomposites reinforced by cellulose nanofibers extracted from paper sludge

Science.gov (United States)

Takagi, Hitoshi; Nakagaito, Antonio N.; Kusaka, Kazuya; Muneta, Yuya

2015-03-01

Cellulose nanofibers have been showing much greater potential to enhance the mechanical and physical properties of polymer-based composite materials. The purpose of this study is to extract the cellulose nanofibers from waste bio-resources; such as waste newspaper and paper sludge. The cellulosic raw materials were treated chemically and physically in order to extract individualized cellulose nanofiber. The combination of acid hydrolysis and following mechanical treatment resulted in the extraction of cellulose nanofibers having diameter of about 40 nm. In order to examine the reinforcing effect of the extracted cellulose nanofibers, fully biodegradable green nanocomposites were fabricated by composing polyvinyl alcohol (PVA) resin with the extracted cellulose nanofibers, and then the tensile tests were conducted. The results showed that the enhancement in mechanical properties was successfully obtained in the cellulose nanofiber/PVA green nanocomposites.

Poly(hydroxybutyrate)/cellulose acetate blend nanofiber scaffolds: Preparation, characterization and cytocompatibility

Energy Technology Data Exchange (ETDEWEB)

Zhijiang, Cai, E-mail: caizhijiang@hotmail.com [School of Textiles, Tianjin Polytechnic University, Tianjin 300387 (China); State Key Laboratory of Hollow Fiber Membrane Material and Processes, No 399 BingShuiXi Street, XiQing District, Tianjin, China, 300387 (China); Yi, Xu; Haizheng, Yang; Jia, Jianru; Liu, Yuanpei [School of Textiles, Tianjin Polytechnic University, Tianjin 300387 (China)

2016-01-01

Poly(hydroxybutyrate) (PHB)/cellulose acetate (CA) blend nanofiber scaffolds were fabricated by electrospinning using the blends of chloroform and DMF as solvent. The blend nanofiber scaffolds were characterized by SEM, FTIR, XRD, DSC, contact angle and tensile test. The blend nanofibers exhibited cylindrical, uniform, bead-free and random orientation with the diameter ranged from 80–680 nm. The scaffolds had very well interconnected porous fibrous network structure and large aspect surface areas. It was found that the presence of CA affected the crystallization of PHB due to formation of intermolecular hydrogen bonds, which restricted the preferential orientation of PHB molecules. The DSC result showed that the PHB and CA were miscible in the blend nanofiber. An increase in the glass transition temperature was observed with increasing CA content. Additionally, the mechanical properties of blend nanofiber scaffolds were largely influenced by the weight ratio of PHB/CA. The tensile strength, yield strength and elongation at break of the blend nanofiber scaffolds increased from 3.3 ± 0.35 MPa, 2.8 ± 0.26 MPa, and 8 ± 0.77% to 5.05 ± 0.52 MPa, 4.6 ± 0.82 MPa, and 17.6 ± 1.24% by increasing PHB content from 60% to 90%, respectively. The water contact angle of blend nanofiber scaffolds decreased about 50% from 112 ± 2.1° to 60 ± 0.75°. The biodegradability was evaluated by in vitro degradation test and the results revealed that the blend nanofiber scaffolds showed much higher degradation rates than the neat PHB. The cytocompatibility of the blend nanofiber scaffolds was preliminarily evaluated by cell adhesion studies. The cells incubated with PHB/CA blend nanofiber scaffold for 48 h were capable of forming cell adhesion and proliferation. It showed much better biocompatibility than pure PHB film. Thus, the prepared PHB/CA blend nanofiber scaffolds are bioactive and may be more suitable for cell proliferation suggesting that these scaffolds can be used for

Cell behaviors on magnetic electrospun poly-D, L-lactide nanofibers

International Nuclear Information System (INIS)

Li, Long; Yang, Guang; Li, Jinrong; Ding, Shan; Zhou, Shaobing

2014-01-01

It is widely accepted that magnetic fields have an influence on cell behaviors, but the effects are still not very clear since the magnetic field's type, intensity and exposure time are different. In this study, a static magnetic field (SMF) in moderate intensity (10 mT) was employed to investigate its effect on osteoblast and 3T3 fibroblast cell behaviors cultured respectively with magnetic polymer nanofiber mats. The magnetic mats composed of random oriented or aligned polymer nanofibers were fabricated by electrospinning the mixed solution of poly-D, L-lactide (PLA) and iron oxide nanoparticles. The fiber morphology was characterized by scanning electron microscopy (SEM), the nanoparticle distribution in fiber matrix was measured with transmission electron microscope (TEM). Mechanical properties of nanofiber mats are studied by uniaxial tensile test. The results showed the nanofibers loaded with magnetic nanoparticles displayed excellent magnetic responsibility and biodegradability. In vitro cytotoxicity analysis demonstrated that the osteoblast proliferation of all fiber mats stimulated with or without SMF was increased with the increase of the culturing days. Furthermore, in the horizontal SMFs, cell orientation tended to deviate from nanofiber orientation to field direction while the nanofiber orientation is perpendicular to the field direction, while the horizonal direction of SMFs could also direct the cell growth orientation. The magnetic nanofiber mats provide a potential platform to explore the cell behaviors under the stimulation of external magnetic field. - Highlights: • The random oriented and aligned magnetic electrospun nanofibers were prepared. • The nanofibers displayed excellent magnetic responsibility and biodegradability. • The horizonal direction of SMFs could also direct the cell growth orientation

Porous TiO_2 nanofibers decorated CdS nanoparticles by SILAR method for enhanced visible-light-driven photocatalytic activity

International Nuclear Information System (INIS)

Tian, Fengyu; Hou, Dongfang; Hu, Fuchao; Xie, Kui; Qiao, Xiuqing; Li, Dongsheng

2017-01-01

Graphical abstract: A heterojunction photocatalyst with CdS Nanoparticles self-assembled via SILAR Method at surfaces of electrospun TiO2 nanofibers shows enhanced visible-light photocatalytic activities. - Highlights: • Combined electrospinning and successive ionic layer adsorption and reaction process. • Pouous TiO_2 nanofibers decorated CdS nanoparticles. • Synergetic effect of photosensitization and heterojunction. - Abstract: 1D porous CdS nanoparticles/TiO_2 nanofibers heterostructure has been fabricated via simple electrospinning and a successive ionic layer adsorption and reaction (SILAR) process. The morphology, composition, and optical properties of the resulting CdS/TiO_2 heterostructures can be rationally tailored through changing the SILAR cycles. The photocatalytic hydrogen evolution and decomposition of rhodamine B (RhB) of the as-synthesized heterostructured photocatalysts were investigated under visible light irradiation. Compared to TiO_2 nanofibers，the as-obtained CdS/TiO_2 heterostructures exhibit enhanced photocatalytic activity for hydrogen production and decomposition of RhB under visible-light irradiation. The heterojunction system performs best with H_2 generation rates of 678.61 μmol h"−"1 g"−"1 under visible light irradiation which benefits from the two effects: (a) the 1D porous nanofibrous morphology contributes to not only more active sites but also more efficient transfer of the photogenerated charges (b) the synergetic effect of heterojunction and photosensitization reducing the recombination of photogenerated electrons and holes.

Novel electrospun gelatin/oxycellulose nanofibers as a suitable platform for lung disease modeling

Energy Technology Data Exchange (ETDEWEB)

Švachová, Veronika, E-mail: xcsvachova@fch.vutbr.cz [Institute of Materials Chemistry, Brno University of Technology (Czech Republic); Vojtová, Lucy [CEITEC – Central European Institute of Technology, Brno University of Technology (Czech Republic); SCITEG, a.s., Brno (Czech Republic); Pavliňák, David [Department of Physical Electronics, Masaryk University (Czech Republic); Vojtek, Libor [Institute of Experimental Biology, Masaryk University (Czech Republic); Sedláková, Veronika [Department of Histology and Embryology, Masaryk University (Czech Republic); International Clinical Research, St. Anne' s University Hospital, Brno (Czech Republic); Hyršl, Pavel [Institute of Experimental Biology, Masaryk University (Czech Republic); Alberti, Milan [Department of Physical Electronics, Masaryk University (Czech Republic); Jaroš, Josef; Hampl, Aleš [Department of Histology and Embryology, Masaryk University (Czech Republic); International Clinical Research, St. Anne' s University Hospital, Brno (Czech Republic); Jančář, Josef [Institute of Materials Chemistry, Brno University of Technology (Czech Republic); CEITEC – Central European Institute of Technology, Brno University of Technology (Czech Republic); SCITEG, a.s., Brno (Czech Republic)

2016-10-01

Novel hydrolytically stable gelatin nanofibers modified with sodium or calcium salt of oxycellulose were prepared by electrospinning method. The unique inhibitory effect of these nanofibers against Escherichia coli bacteria was examined by luminometric method. Biocompatibility of these gelatin/oxycellulose nanofibers with eukaryotic cells was tested using human lung adenocarcinoma cell line NCI-H441. Cells firmly adhered to nanofiber surface, as determined by scanning electron microscopy, and no signs of cell dying were detected by fluorescent live/dead assay. We propose that the newly developed gelatin/oxycellulose nanofibers could be used as promising scaffold for lung disease modeling and anti-cancer drug testing. - Highlights: • Novel hydrolytically stable gelatin nanofibers modified with oxycellulose were prepared by electrospinning. • ATR–FTIR spectroscopy and EDX confirmed the presence of oxycellulose in the nanofibers. • Nanofibers modified with calcium salt of oxycellulose exhibited significant antibacterial properties. • Nanofibers modified with sodium salt of oxycellulose revealed excellent biocompatibility with cell line NCI-H441.

Magnetized graphene layers synthesized on the carbon nanofibers as novel adsorbent for the extraction of polycyclic aromatic hydrocarbons from environmental water samples.

Science.gov (United States)

Rezvani-Eivari, Mostafa; Amiri, Amirhassan; Baghayeri, Mehdi; Ghaemi, Ferial

2016-09-23

The application of magnetized graphene (G) layers synthesized on the carbon nanofibers (CNFs) (m-G/CNF) was investigated as novel adsorbent for the magnetic solid-phase extraction (MSPE) of polycyclic aromatic hydrocarbons (PAHs) in water samples followed by gas chromatography-flame ionization detector (GC-FID). Six important parameters, affecting the extraction efficiency of PAHs, including: amount of adsorbent, adsorption and desorption times, type and volume of the eluent solvent and salt content of the sample were evaluated. The optimum extraction conditions were obtained as: 5min for extraction time, 20mg for sorbent amount, dichloromethane as desorption solvent, 1mL for desorption solvent volume, 5min for desorption time and 15% (w/v) for NaCl concentration. Good performance data were obtained at the optimized conditions. The calibration curves were linear over the concentration ranges from 0.012 to 100ngmL(-1) with correlation coefficients (r) between 0.9950 and 0.9967 for all the analytes. The limits of detection (LODs, S/N=3) of the proposed method for the studied PAHs were 0.004-0.03ngmL(-1). The relative standard deviations (RSDs) for five replicates at two concentration levels (0.1 and 50ngmL(-1)) of PAHs were ranged from 3.4 to 5.7%. Appropriate relative recovery values, in the range of 95.5-99.9%, were also obtained for the real water sample analysis. Copyright © 2016 Elsevier B.V. All rights reserved.

Field-enhanced nonlinear optical properties of organic nanofibers

DEFF Research Database (Denmark)

Kostiučenko, Oksana; Fiutowski, Jacek; Brewer, Jonathan R.

2014-01-01

Second harmonic generation in nonlinearly optically active organic nanofibers, generated via self-assembled surface growth from nonsymmetrically functionalized para-quarterphenylene (CNHP4) molecules, has been investigated. After the growth on mica templates, nanofibers have been transferred onto...

Fluorescent and Colorimetric Electrospun Nanofibers for Heavy-Metal Sensing

Directory of Open Access Journals (Sweden)

Idelma A. A. Terra

2017-12-01

Full Text Available The accumulation of heavy metals in the human body and/or in the environment can be highly deleterious for mankind, and currently, considerable efforts have been made to develop reliable and sensitive techniques for their detection. Among the detection methods, chemical sensors appear as a promising technology, with emphasis on systems employing optically active nanofibers. Such nanofibers can be obtained by the electrospinning technique, and further functionalized with optically active chromophores such as dyes, conjugated polymers, carbon-based nanomaterials and nanoparticles, in order to produce fluorescent and colorimetric nanofibers. In this review we survey recent investigations reporting the use of optically active electrospun nanofibers in sensors aiming at the specific detection of heavy metals using colorimetry and fluorescence methods. The examples given in this review article provide sufficient evidence of the potential of optically electrospun nanofibers as a valid approach to fabricate highly selective and sensitive optical sensors for fast and low-cost detection of heavy metals.

Nanofiber Nerve Guide for Peripheral Nerve Repair and Regeneration

Science.gov (United States)

2016-04-01

1 Award Number: W81XWH-11-2-0047 TITLE: Nanofiber Nerve Guide for Peripheral Nerve Repair and Regeneration PRINCIPAL INVESTIGATOR: Ahmet Höke...TITLE AND SUBTITLE 5a. CONTRACT NUMBER W81XWH-11-2-0047 Nanofiber nerve guide for peripheral nerve repair and regeneration 5b. GRANT NUMBER...goal of this collaborative research project was to develop next generation engineered nerve guide conduits (NGCs) with aligned nanofibers and

Dry adhesives from carbon nanofibers grown in an open ethanol flame

Directory of Open Access Journals (Sweden)

Christian Lutz

2017-12-01

Full Text Available Based on magnetic-field-assisted growth of carbon nanofibers in an open ethanol flame we fabricated arrays of carbon nanofibers with different degrees of orientation. Inspired by the dry adhesive system of geckos we investigated the adhesive properties of such carbon nanofiber arrays with ordered and random orientation. AFM-based force spectroscopy revealed that adhesion force and energy rise linear with preload force. Carbon nanofibers oriented by a magnetic field show a 68% higher adhesion (0.66 N/cm2 than the randomly oriented fibers. Endurance tests revealed that the carbon nanofiber arrays withstand 50.000 attachment/detachment cycles without observable wear.

Hybrid electrospun chitosan-phospholipids nanofibers for transdermal drug delivery

DEFF Research Database (Denmark)

Mendes, Ana Carina Loureiro; Gorzelanny, Christian; Halter, Natalia

2016-01-01

Chitosan (Ch) polysaccharide was mixed with phospholipids (P) to generate electrospun hybrid nanofibers intended to be used as platforms for transdermal drug delivery. Ch/P nanofibers exibithed average diameters ranging from 248 +/- 94 nm to 600 +/- 201 nm, depending on the amount of phospholipids...... used. Fourier Transformed Infra-Red (FTIR) spectroscopy and Dynamic Light Scattering (DLS) data suggested the occurrence of electrostatic interactions between amine groups of chitosan with the phospholipid counterparts. The nanofibers were shown to be stable for at least 7 days in Phosphate Buffer...... culture plate (control). The release of curcumin, diclofenac and vitamin B12, as model drugs, from Ch/P hybrid nanofibers was investigated, demonstrating their potential utilization as a transdermal drug delivery system....

Synthesis and characterization of crosslinked gellan/PVA nanofibers for tissue engineering application.

Science.gov (United States)

Vashisth, Priya; Pruthi, Vikas

2016-10-01

Electrospun nanofibers based on gellan are considered as promising biomaterial for tissue engineering and wound healing applications. However, major hurdles in usage of these nanofibers are their poor stability and deprived structural consistency in aqueous medium which is a prerequisite for their application in the biomedical sector. In this investigation, three dimensional nanofibers, consisting of gellan and PVA have been fabricated and then stabilized under various crosslinking conditions in order to improve their physiochemical stability. The impacts of different crosslinking procedures on the gellan/PVA nanofibers were examined in terms of changes in morphological, mechanical, swelling and biological properties. Superior tensile strength and strain was recorded in case of crosslinked nanofibers as compared to non-crosslinked nanofibers. Contact angles and swelling properties of fabricated gellan/PVA nanofibers were found to vary with the crosslinking method. All crosslinking conditions were evaluated with regard to their response towards human dermal fibroblast (3T3L1) cells. Biocompatibility studies suggested that the fabricated crosslinked gellan/PVA nanofibers hold a great prospective in the biomedical engineering arena. Copyright © 2016 Elsevier B.V. All rights reserved.

Preparation of porous carbon nanofibers derived from PBI/PLLA for supercapacitor electrodes.

Science.gov (United States)

Jung, Kyung-Hye; Ferraris, John P

2016-10-21

Porous carbon nanofibers were prepared by electrospinning blend solutions of polybenzimidazole/poly-L-lactic acid (PBI/PLLA) and carbonization. During thermal treatment, PLLA was decomposed, resulting in the creation of pores in the carbon nanofibers. From SEM images, it is shown that carbon nanofibers had diameters in the range of 100-200 nm. The conversion of PBI to carbon was confirmed by Raman spectroscopy, and the surface area and pore volume of carbon nanofibers were determined using nitrogen adsorption/desorption analyses. To investigate electrochemical performances, coin-type cells were assembled using free-standing carbon nanofiber electrodes and ionic liquid electrolyte. cyclic voltammetry studies show that the PBI/PLLA-derived porous carbon nanofiber electrodes have higher capacitance due to lower electrochemical impedance compared to carbon nanofiber electrode from PBI only. These porous carbon nanofibers were activated using ammonia for further porosity improvement and annealed to remove the surface functional groups to better match the polarity of electrode and electrolyte. Ragone plots, correlating energy density with power density calculated from galvanostatic charge-discharge curves, reveal that activation/annealing further improves energy and power densities.

Solution-blown nanofiber mats from fish sarcoplasmic protein

DEFF Research Database (Denmark)

Sett, S.; Boutrup Stephansen, Karen; Yarin, A.L.

2016-01-01

In the present work, solution-blowing was adopted to form nanofibers from fish sarcoplasmic proteins (FSPs). Nanofiber mats containing different weight ratios (up to 90/10) of FSP in the FSP/nylon 6 blended nanofibers were formed from formic acid solutions, and compared to electrospun fibers made...... that the production rate of solution-blowing was increased 30-fold in relation to electrospinning. Overall, this study reveals FSP as an interesting biopolymeric alternative to synthetic polymers, and the introduction of FSP to nylon 6 provides a composite with controlled properties....

Layer-by-layer assembled polyaniline nanofiber/multiwall carbon nanotube thin film electrodes for high-power and high-energy storage applications.

Science.gov (United States)

Hyder, Md Nasim; Lee, Seung Woo; Cebeci, Fevzi Ç; Schmidt, Daniel J; Shao-Horn, Yang; Hammond, Paula T

2011-11-22

Thin film electrodes of polyaniline (PANi) nanofibers and functionalized multiwall carbon nanotubes (MWNTs) are created by layer-by-layer (LbL) assembly for microbatteries or -electrochemical capacitors. Highly stable cationic PANi nanofibers, synthesized from the rapid aqueous phase polymerization of aniline, are assembled with carboxylic acid functionalized MWNT into LbL films. The pH-dependent surface charge of PANi nanofibers and MWNTs allows the system to behave like weak polyelectrolytes with controllable LbL film thickness and morphology by varying the number of bilayers. The LbL-PANi/MWNT films consist of a nanoscale interpenetrating network structure with well developed nanopores that yield excellent electrochemical performance for energy storage applications. These LbL-PANi/MWNT films in lithium cell can store high volumetric capacitance (~238 ± 32 F/cm(3)) and high volumetric capacity (~210 mAh/cm(3)). In addition, rate-dependent galvanostatic tests show LbL-PANi/MWNT films can deliver both high power and high energy density (~220 Wh/L(electrode) at ~100 kW/L(electrode)) and could be promising positive electrode materials for thin film microbatteries or electrochemical capacitors. © 2011 American Chemical Society

Polymeric Nanofibers with Ultrahigh Piezoelectricity via Self-Orientation of Nanocrystals.

Science.gov (United States)

Liu, Xia; Ma, Jing; Wu, Xiaoming; Lin, Liwei; Wang, Xiaohong

2017-02-28

Piezoelectricity in macromolecule polymers has been gaining immense attention, particularly for applications in biocompatible, implantable, and flexible electronic devices. This paper introduces core-shell-structured piezoelectric polyvinylidene fluoride (PVDF) nanofibers chemically wrapped by graphene oxide (GO) lamellae (PVDF/GO nanofibers), in which the polar β-phase nanocrystals are formed and uniaxially self-oriented by the synergistic effect of mechanical stretching, high-voltage alignment, and chemical interactions. The β-phase orientation of the PVDF/GO nanofibers along their axes is observed at atomic scale through high resolution transmission electron microscopy, and the β-phase content is found to be 88.5%. The piezoelectric properties of the PVDF/GO nanofibers are investigated in terms of piezoresponse mapping, local hysteresis loops, and polarization reversal by advanced piezoresponse force microscopy. The PVDF/GO nanofibers show a desirable out-of-plane piezoelectric constant (d 33 ) of -93.75 pm V -1 (at 1.0 wt % GO addition), which is 426% higher than that of the conventional pure PVDF nanofibers. The mechanism behind this dramatic enhancement in piezoelectricity is elucidated by three-dimensional molecular modeling.

Electrospun water-stable zein/ethyl cellulose composite nanofiber and its drug release properties

Energy Technology Data Exchange (ETDEWEB)

Lu, Hangyi; Wang, Qingqing; Li, Guohui [Key Laboratory of Eco-textiles, Jiangnan University, Wuxi (China); Qiu, Yuyu [Key Laboratory of Eco-textiles, Jiangnan University, Wuxi (China); Laboratory of Natural Medicine, Wuxi Medical School, Jiangnan University (China); Wei, Qufu, E-mail: qfwei@jiangnan.edu.cn [Key Laboratory of Eco-textiles, Jiangnan University, Wuxi (China)

2017-05-01

A simple and cost-effective way to prepare water-stable zein-based nanofibers for potential drug delivery was presented in this article. Corn protein zein was co-electrospun with hydrophobic ethyl cellulose. Indomethacin, as a model drug, was incorporated in situ into the composite nanofibers. Scanning electron microscopy and element mapping revealed the morphologies of drug-loaded nanofibers and drug distribution, respectively. Fourier transform infrared spectra confirmed the physical blending among the components. Differential scanning calorimetry and X-ray diffraction demonstrated the physical state of drug and polymers in the nanofiber matrix. The composite nanofibers showed a sustained diffusion-controlled release according to the results of in vitro dissolution tests. - Highlights: • A simple, non-toxic and cost-effective way to improve water stability of zein nanofibers was proposed. • Electrospun zein/ethyl cellulose nanofibers with improved water stability and mechanical strength were prepared. • Indomethacin was homogeneously distributed in the zein/ethyl cellulose nanofibers with no aggregation or cluster. • The zein/ethyl cellulose nanofibers presented a sustained drug release profile, following Fickican diffusion mechanism.

Nanofiber Anisotropic Conductive Films (ACF) for Ultra-Fine-Pitch Chip-on-Glass (COG) Interconnections

Science.gov (United States)

Lee, Sang-Hoon; Kim, Tae-Wan; Suk, Kyung-Lim; Paik, Kyung-Wook

2015-11-01

Nanofiber anisotropic conductive films (ACF) were invented, by adapting nanofiber technology to ACF materials, to overcome the limitations of ultra-fine-pitch interconnection packaging, i.e. shorts and open circuits as a result of the narrow space between bumps and electrodes. For nanofiber ACF, poly(vinylidene fluoride) (PVDF) and poly(butylene succinate) (PBS) polymers were used as nanofiber polymer materials. For PVDF and PBS nanofiber ACF, conductive particles of diameter 3.5 μm were incorporated into nanofibers by electrospinning. In ultra-fine-pitch chip-on-glass assembly, insulation was significantly improved by using nanofiber ACF, because nanofibers inside the ACF suppressed the mobility of conductive particles, preventing them from flowing out during the bonding process. Capture of conductive particles was increased from 31% (conventional ACF) to 65%, and stable electrical properties and reliability were achieved by use of nanofiber ACF.

A smart core-sheath nanofiber that captures and releases red blood cells from the blood

Science.gov (United States)

Shi, Q.; Hou, J.; Zhao, C.; Xin, Z.; Jin, J.; Li, C.; Wong, S.-C.; Yin, J.

2016-01-01

A smart core-sheath nanofiber for non-adherent cell capture and release is demonstrated. The nanofibers are fabricated by single-spinneret electrospinning of poly(N-isopropylacrylamide) (PNIPAAm), polycaprolactone (PCL) and nattokinase (NK) solution blends. The self-assembly of PNIPAAm and PCL blends during the electrospinning generates the core-sheath PCL/PNIPAAm nanofibers with PNIPAAm as the sheath. The PNIPAAm-based core-sheath nanofibers are switchable between hydrophobicity and hydrophilicity with temperature change and enhance stability in the blood. When the nanofibers come in contact with blood, the NK is released from the nanofibers to resist platelet adhesion on the nanofiber surface, facilitating the direct capture and isolation of red blood cells (RBCs) from the blood above phase-transition temperature of PNIPAAm. Meanwhile, the captured RBCs are readily released from the nanofibers with temperature stimuli in an undamaged manner. The release efficiency of up to 100% is obtained while maintaining cellular integrity and function. This work presents promising nanofibers to effectively capture non-adherent cells and release for subsequent molecular analysis and diagnosis of single cells.A smart core-sheath nanofiber for non-adherent cell capture and release is demonstrated. The nanofibers are fabricated by single-spinneret electrospinning of poly(N-isopropylacrylamide) (PNIPAAm), polycaprolactone (PCL) and nattokinase (NK) solution blends. The self-assembly of PNIPAAm and PCL blends during the electrospinning generates the core-sheath PCL/PNIPAAm nanofibers with PNIPAAm as the sheath. The PNIPAAm-based core-sheath nanofibers are switchable between hydrophobicity and hydrophilicity with temperature change and enhance stability in the blood. When the nanofibers come in contact with blood, the NK is released from the nanofibers to resist platelet adhesion on the nanofiber surface, facilitating the direct capture and isolation of red blood cells (RBCs) from

Nanoparticles and nanofibers for topical drug delivery

Science.gov (United States)

Goyal, Ritu; Macri, Lauren K.; Kaplan, Hilton M.; Kohn, Joachim

2016-01-01

This review provides the first comprehensive overview of the use of both nanoparticles and nanofibers for topical drug delivery. Researchers have explored the use of nanotechnology, specifically nanoparticles and nanofibers, as drug delivery systems for topical and transdermal applications. This approach employs increased drug concentration in the carrier, in order to increase drug flux into and through the skin. Both nanoparticles and nanofibers can be used to deliver hydrophobic and hydrophilic drugs and are capable of controlled release for a prolonged period of time. The examples presented provide significant evidence that this area of research has—and will continue to have — a profound impact on both clinical outcomes and the development of new products. PMID:26518723

Binder-free Si nanoparticles@carbon nanofiber fabric as energy storage material

International Nuclear Information System (INIS)

Liu, Yuping; Huang, Kai; Fan, Yu; Zhang, Qing; Sun, Fu; Gao, Tian; Wang, Zhongzheng; Zhong, Jianxin

2013-01-01

A nonwoven nanofiber fabric with paper-like qualities composed of Si nanoparticles and carbon as binder-free anode electrode is reported. The nanofiber fabrics are prepared by convenient electrospinning technique, in which, the Si nanoparticles are uniformly confined in the carbon nanofibers. The high strength and flexibility of the nanofiber fabrics are beneficial for alleviating the structural deformation and facilitating ion transports throughout the whole composited electrodes. Due to the absence of binder, the less weight, higher energy density, and excellent electrical conductivity anodes can be attained. These traits make the composited nanofiber fabrics excellent used as a binder-free, mechanically flexible, high energy storage anode material in the next generation of rechargeable lithium ions batteries

Porous TiO{sub 2} nanofibers decorated CdS nanoparticles by SILAR method for enhanced visible-light-driven photocatalytic activity

Energy Technology Data Exchange (ETDEWEB)

Tian, Fengyu; Hou, Dongfang, E-mail: dfhouok@126.com; Hu, Fuchao; Xie, Kui; Qiao, Xiuqing; Li, Dongsheng, E-mail: lidongsheng1@126.com

2017-01-01

Graphical abstract: A heterojunction photocatalyst with CdS Nanoparticles self-assembled via SILAR Method at surfaces of electrospun TiO2 nanofibers shows enhanced visible-light photocatalytic activities. - Highlights: • Combined electrospinning and successive ionic layer adsorption and reaction process. • Pouous TiO{sub 2} nanofibers decorated CdS nanoparticles. • Synergetic effect of photosensitization and heterojunction. - Abstract: 1D porous CdS nanoparticles/TiO{sub 2} nanofibers heterostructure has been fabricated via simple electrospinning and a successive ionic layer adsorption and reaction (SILAR) process. The morphology, composition, and optical properties of the resulting CdS/TiO{sub 2} heterostructures can be rationally tailored through changing the SILAR cycles. The photocatalytic hydrogen evolution and decomposition of rhodamine B (RhB) of the as-synthesized heterostructured photocatalysts were investigated under visible light irradiation. Compared to TiO{sub 2} nanofibers，the as-obtained CdS/TiO{sub 2} heterostructures exhibit enhanced photocatalytic activity for hydrogen production and decomposition of RhB under visible-light irradiation. The heterojunction system performs best with H{sub 2} generation rates of 678.61 μmol h{sup −1} g{sup −1} under visible light irradiation which benefits from the two effects: (a) the 1D porous nanofibrous morphology contributes to not only more active sites but also more efficient transfer of the photogenerated charges (b) the synergetic effect of heterojunction and photosensitization reducing the recombination of photogenerated electrons and holes.

Development of Protective Clothing against Nanoparticle Based on Electrospun Nanofibers

Directory of Open Access Journals (Sweden)

M. Faccini

2012-01-01

Full Text Available In this paper, the development of efficient protective clothing against nanoparticulate aerosols is presented. Nanofibrous mats of polyamide 6 (PA6 were deposited onto a nonwoven viscose substrate by electrospinning technique. The influence of electrospinning parameters, including solution concentration, viscosity, and conductivity, was studied for the production of nonwovens with controlled fiber diameter showing a size distribution ranging from 66 to 195 nm. By varying several process parameters, textiles with different thickness of the nanofiber layer and thus air permeability were obtained. A hot-press lamination process using a thermoplastic resin as glue was applied to improve the adhesion of the nanofiber layer onto the textile support. After 1500 cycles of repeated compression and torsion, the nanofiber layer was still firmly attached to the support, while mechanical damage is visible in some areas. The penetration of NaCl particles with diameter ranging from 15 to 300 nm through the electrospun textiles was found to be strongly dependent on nanofiber layer thickness. A really thin nanofiber coating provides up to 80% retention of 20 nm size particles and over 50% retention of 200 nm size nanoparticles. Increasing the thickness of the nanofiber mat, the filtration efficiency was increased to over 99% along the whole nanoparticle range. The results obtained highlight the potential of nanofibers in the development of efficient personal protective equipments against nanoparticles.

Biomedical Applications of Antibacterial Nanofiber Mats Made of Electrospinning with Wire Electrodes

Directory of Open Access Journals (Sweden)

Yi-Jun Pan

2016-02-01

Full Text Available Twisted stainless steel wires are used as wire electrodes for electrospinning the polyvinyl alcohol (PVA/zinc citrate nanofiber mats. The morphology and diameter of the nanofibers in PVA/zinc citrate nanofiber mats are evaluated. We measured the antibacterial efficacy against Staphylococcus aureus (S. aureus and Escherichia coli (E. coli of the nanofiber mats. We also examined the cell adhesion affinity of mammalian tissue culture cells on these nanofiber mats. Our results indicate that an increase in zinc citrate increases the viscosity and electrical conductivity of PVA solution. In addition, increasing zinc citrate results in a smaller diameter of nanofibers that reaches below 100 nm. According to the antibacterial test results, increasing zinc citrate enlarges the inhibition zone of S. aureus but only has a bacteriostatic effect against E. coli. Finally, cell adhesion test results indicate that all nanofiber mats have satisfactory cell attachment regardless of the content of zinc citrate.

Electrospun single-walled carbon nanotube/polyvinyl alcohol composite nanofibers: structure-property relationships

International Nuclear Information System (INIS)

Naebe, Minoo; Lin Tong; Wang Xungai; Staiger, Mark P; Dai Liming

2008-01-01

Polyvinyl alcohol (PVA) nanofibers and single-walled carbon nanotube (SWNT)/PVA composite nanofibers have been produced by electrospinning. An apparent increase in the PVA crystallinity with a concomitant change in its main crystalline phase and a reduction in the crystalline domain size were observed in the SWNT/PVA composite nanofibers, indicating the occurrence of a SWNT-induced nucleation crystallization of the PVA phase. Both the pure PVA and SWNT/PVA composite nanofibers were subjected to the following post-electrospinning treatments: (i) soaking in methanol to increase the PVA crystallinity, and (ii) cross-linking with glutaric dialdehyde to control the PVA morphology. Effects of the PVA morphology on the tensile properties of the resultant electrospun nanofibers were examined. Dynamic mechanical thermal analyses of both pure PVA and SWNT/PVA composite electrospun nanofibers indicated that SWNT-polymer interaction facilitated the formation of crystalline domains, which can be further enhanced by soaking the nanofiber in methanol and/or cross-linking the polymer with glutaric dialdehyde

Orthorhombic phase formation in electrochemically grown vanadium oxide (V{sub 2}O{sub 5}) nanofibers

Energy Technology Data Exchange (ETDEWEB)

Langie da Silva, Douglas, E-mail: douglas.langie@ufpel.edu.br [Departamento de Física, Universidade Federal de Pelotas, Caixa Postal 354, Pelotas 96010-900 (Brazil); Pasa, André Avelino [Laboratório de Filmes Finos e Superfícies, Departamento de Física, Universidade Federal de Santa Catarina, Caixa Postal 476, Florianópolis 88.040-900 (Brazil)

2013-06-15

The inner structure of V{sub 2}O{sub 5} nanofibers synthesized by electrochemical deposition has been investigated by transmission electron microscopy (TEM) and selected area electron diffraction (SAED). The experimental results demonstrate that the fibers are formed by 2D orthorhombic layers of V{sub 2}O{sub 5}. The layers are formed along the plane ab stacked in the crystallographic direction c. Additionally the diffraction results indicate that the fibers grow preferentially along the (100) crystallographic plane with surface dominated by the plane (001). The formation of fibers is discussed in terms of the preferential growth along specific orientations in order to minimize the surface energy of the nanostructures. - Highlights: • Electrochemical deposition leads to the formation of 2D crystalline V{sub 2}O{sub 5} nanofibers. • Electron diffraction was used to determine the inner structure of fibers. • The fibers grown preferentially along the low-index (100) crystallographic plane. • The fibers grow along specific orientations in order to minimize the surface energy. • The 2D structure of fibers is an important feature for technological applications.

Optics of Nanofibers

DEFF Research Database (Denmark)

Bordo, Vladimir

During the last decade, fabrication and investigation of submicron-sized optical fibers have been received growing attention. Such nanofibers or nanowires can be grown from both inorganic and organic semiconductor materials being arranged in mutually parallel nanoaggregates. Also, selected...

Growth and characterization of hydroxyapatite nanorice on TiO2 nanofibers

KAUST Repository

Chetibi, Loubna; Hamana, Djamel; Achour, Slimane

2014-01-01

with anatase TiO2 nanofibers. These nanofibers were prepared by in situ oxidation of Ti foils in a concentrated solution of H 2O2 and NaOH, followed by proton exchange and calcinations. Afterward, TiO2 nanofibers on Ti substrate were coated with HA

Hybrid electrospun chitosan-phospholipids nanofibers for transdermal drug delivery.

Science.gov (United States)

Mendes, Ana C; Gorzelanny, Christian; Halter, Natalia; Schneider, Stefan W; Chronakis, Ioannis S

2016-08-20

Chitosan (Ch) polysaccharide was mixed with phospholipids (P) to generate electrospun hybrid nanofibers intended to be used as platforms for transdermal drug delivery. Ch/P nanofibers exibithed average diameters ranging from 248±94nm to 600±201nm, depending on the amount of phospholipids used. Fourier Transformed Infra-Red (FTIR) spectroscopy and Dynamic Light Scattering (DLS) data suggested the occurrence of electrostatic interactions between amine groups of chitosan with the phospholipid counterparts. The nanofibers were shown to be stable for at least 7days in Phosphate Buffer Saline (PBS) solution. Cytotoxicity studies (WST-1 and LDH assays) demonstrated that the hybrid nanofibers have suitable biocompatibility. Fluorescence microscopy, also suggested that L929 cells seeded on top of the CH/P hybrid have similar metabolic activity comparatively to the cells seeded on tissue culture plate (control). The release of curcumin, diclofenac and vitamin B12, as model drugs, from Ch/P hybrid nanofibers was investigated, demonstrating their potential utilization as a transdermal drug delivery system. Copyright © 2016 Elsevier B.V. All rights reserved.

Fabrication of Cationic Exchange Polystyrene Nanofibers for Drug ...

African Journals Online (AJOL)

Purpose: To prepare polystyrene nanofiber ion exchangers (PSNIE) with surface cation exchange functionality using a new method based on electrospinning and also to optimize crosslinking and sulfonation reactions to obtain PSNIE with maximum ion exchange capacity (IEC). Method: The nanofibers were prepared from ...

Electrospun Fe3O4/TiO2 hybrid nanofibers and their in vitro biocompatibility: prospective matrix for satellite cell adhesion and cultivation.

Science.gov (United States)

Amna, Touseef; Hassan, M Shamshi; Van Ba, Hoa; Khil, Myung-Seob; Lee, Hak-Kyo; Hwang, I H

2013-03-01

We report the fabrication of novel Fe3O4/TiO2 hybrid nanofibers with the improved cellular response for potential tissue engineering applications. In this study, Fe3O4/TiO2 hybrid nanofibers were prepared by facile sol-gel electrospinning using titanium isopropoxide and iron(III) nitrate nonahydrate as precursors. The obtained electrospun nanofibers were vacuum dried at 80 °C and then calcined at 500 °C. The physicochemical characterization of the synthesized composite nanofibers was carried out by scanning electron microscopy, energy dispersive X-ray spectroscopy, transmission electron microscopy and X-ray diffraction pattern. To examine the in vitro cytotoxicity, satellite cells were treated with as-prepared Fe3O4/TiO2 and the viability of cells was analyzed by Cell Counting Kit-8 assay at regular time intervals. The morphological features of unexposed satellite cells and exposed to Fe3O4/TiO2 composite were examined with a phase contrast microscope whereas the quantification of cell viability was carried out via confocal laser scanning microscopy. The morphology of the cells attached to hybrid matrix was observed by Bio-SEM. Cytotoxicity experiments indicated that the satellite cells could attach to the Fe3O4/TiO2 composite nanofibers after being cultured. We observed that Fe3O4-TiO2 composite nanofibers could support cell adhesion and growth. Results from this study therefore suggest that Fe3O4/TiO2 composite scaffold with small diameters (approximately 200 nm) can mimic the natural extracellular matrix well and provide possibilities for diverse applications in the field of tissue engineering and regenerative medicine. Copyright © 2012 Elsevier B.V. All rights reserved.

Nanofiber scaffolds influence organelle structure and function in bone marrow stromal cells.

Science.gov (United States)

Tutak, Wojtek; Jyotsnendu, Giri; Bajcsy, Peter; Simon, Carl G

2017-07-01

Recent work demonstrates that osteoprogenitor cell culture on nanofiber scaffolds can promote differentiation. This response may be driven by changes in cell morphology caused by the three-dimensional (3D) structure of nanofibers. We hypothesized that nanofiber effects on cell behavior may be mediated by changes in organelle structure and function. To test this hypothesis, human bone marrow stromal cells (hBMSCs) were cultured on poly(ε-caprolactone) (PCL) nanofibers scaffolds and on PCL flat spuncoat films. After 1 day-culture, hBMSCs were stained for actin, nucleus, mitochondria, and peroxisomes, and then imaged using 3D confocal microscopy. Imaging revealed that the hBMSC cell body (actin) and peroxisomal volume were reduced during culture on nanofibers. In addition, the nucleus and peroxisomes occupied a larger fraction of cell volume during culture on nanofibers than on films, suggesting enhancement of the nuclear and peroxisomal functional capacity. Organelles adopted morphologies with greater 3D-character on nanofibers, where the Z-Depth (a measure of cell thickness) was increased. Comparisons of organelle positions indicated that the nucleus, mitochondria, and peroxisomes were closer to the cell center (actin) for nanofibers, suggesting that nanofiber culture induced active organelle positioning. The smaller cell volume and more centralized organelle positioning would reduce the energy cost of inter-organelle vesicular transport during culture on nanofibers. Finally, hBMSC bioassay measurements (DNA, peroxidase, bioreductive potential, lactate, and adenosine triphosphate (ATP)) indicated that peroxidase activity may be enhanced during nanofiber culture. These results demonstrate that culture of hBMSCs on nanofibers caused changes in organelle structure and positioning, which may affect organelle functional capacity and transport. Published 2016. This article is a U.S. Government work and is in the public domain in the USA. J Biomed Mater Res Part B: Appl

Flexible Fe2O3 and V2O5 nanofibers as binder-free electrodes for high-performance all-solid-state asymmetric supercapacitors.

Science.gov (United States)

Jiang, He; Niu, Hao; Yang, Xue; Sun, Zhiqin; Li, Fuzhi; Wang, Qian; Qu, Fengyu

2018-04-16

Flexible highly porous Fe2O3 and V2O5 nanofibers are synthesized by a facile electrospinning method followed by calcination treatment and directly used as binder-free electrodes for high-performance supercapacitors. These Fe2O3 and V2O5 nanofibers interconnect with each other and construct three-dimensional hierarchical porous films with high specific surface area. Benefiting from the unique structural features, the intriguing binder-free Fe2O3 and V2O5 porous nanofiber electrodes possess high specific capacitance of 255 F g-1 and 256 F g-1 at 2 mV s-1 in 1 M Na2SO4 electrolyte, respectively. An all-solid-state asymmetric supercapacitor is fabricated using Fe2O3 and V2O5 nanofibers as negative and positive electrodes, respectively, and the all-solid-state asymmetric supercapacitor can be operated up to 1.8 V attributed to the wide and opposite potential window of both electrodes. The assembled all-solid-state asymmetric supercapacitor achieves a high energy density up to 32.2 Wh kg-1 at an average power density of 128.7 W kg-1 as well as excellent cycling stability and power capability. The effective and facile synthesis method and superior electrochemical performance provided in this work make electrospun Fe2O3 and V2O5 nanofibers promising electrode materials for high performance asymmetric supercapacitors. © 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Preparation of Fish Skin Gelatin-Based Nanofibers Incorporating Cinnamaldehyde by Solution Blow Spinning

Science.gov (United States)

Liu, Fei; Avena-Bustillos, Roberto J.; Bridges, David F.; Takeoka, Gary R.; Wu, Vivian C. H.; Chiou, Bor-Sen; McHugh, Tara H.; Zhong, Fang

2018-01-01

Cinnamaldehyde, a natural preservative that can non-specifically deactivate foodborne pathogens, was successfully incorporated into fish skin gelatin (FSG) solutions and blow spun into uniform nanofibers. The effects of cinnamaldehyde ratios (5–30%, w/w FSG) on physicochemical properties of fiber-forming emulsions (FFEs) and their nanofibers were investigated. Higher ratios resulted in higher values in particle size and viscosity of FFEs, as well as higher values in diameter of nanofibers. Loss of cinnamaldehyde was observed during solution blow spinning (SBS) process and cinnamaldehyde was mainly located on the surface of resultant nanofibers. Nanofibers all showed antibacterial activity by direct diffusion and vapor release against Escherichia coli O157:H7, Salmonella typhimurium, and Listeria monocytogenes. Inhibition zones increased as cinnamaldehyde ratio increased. Nanofibers showed larger inhibition effects than films prepared by casting method when S. typhimurium was exposed to the released cinnamaldehyde vapor, although films had higher remaining cinnamaldehyde than nanofibers after preparation. Lower temperature was favorable for cinnamaldehyde retention, and nanofibers added with 10% cinnamaldehyde ratio showed the highest retention over eight-weeks of storage. Results suggest that FSG nanofibers can be prepared by SBS as carriers for antimicrobials. PMID:29470390

Preparation of Fish Skin Gelatin-Based Nanofibers Incorporating Cinnamaldehyde by Solution Blow Spinning.

Science.gov (United States)

Liu, Fei; Türker Saricaoglu, Furkan; Avena-Bustillos, Roberto J; Bridges, David F; Takeoka, Gary R; Wu, Vivian C H; Chiou, Bor-Sen; Wood, Delilah F; McHugh, Tara H; Zhong, Fang

2018-02-22

Cinnamaldehyde, a natural preservative that can non-specifically deactivate foodborne pathogens, was successfully incorporated into fish skin gelatin (FSG) solutions and blow spun into uniform nanofibers. The effects of cinnamaldehyde ratios (5-30%, w / w FSG) on physicochemical properties of fiber-forming emulsions (FFEs) and their nanofibers were investigated. Higher ratios resulted in higher values in particle size and viscosity of FFEs, as well as higher values in diameter of nanofibers. Loss of cinnamaldehyde was observed during solution blow spinning (SBS) process and cinnamaldehyde was mainly located on the surface of resultant nanofibers. Nanofibers all showed antibacterial activity by direct diffusion and vapor release against Escherichia coli O157:H7 , Salmonella typhimurium , and Listeria monocytogenes . Inhibition zones increased as cinnamaldehyde ratio increased. Nanofibers showed larger inhibition effects than films prepared by casting method when S . typhimurium was exposed to the released cinnamaldehyde vapor, although films had higher remaining cinnamaldehyde than nanofibers after preparation. Lower temperature was favorable for cinnamaldehyde retention, and nanofibers added with 10% cinnamaldehyde ratio showed the highest retention over eight-weeks of storage. Results suggest that FSG nanofibers can be prepared by SBS as carriers for antimicrobials.

Antibacterial polylactic acid/chitosan nanofibers decorated with bioactive glass

Energy Technology Data Exchange (ETDEWEB)

Goh, Yi-fan; Akram, Muhammad; Alshemary, Ammarz [Department of Chemistry, Faculty of Science, Universiti Teknologi Malaysia, 81310 Johor Bahru, Johor (Malaysia); Hussain, Rafaqat, E-mail: rafaqat@comsats.edu.pk [Department of Physics, COMSATS Institute of Information Technology, Islamabad (Pakistan)

2016-11-30

Highlights: • PLA/Chitosan nanofibers were coated with functional bioglass. • Polymer/ceramic composite fibers exhibited good in-vitro bioactivity. • Nanofibers coated with Ag doped bioglass exhibited good antibacterial activity. - Abstract: In this study, we have presented the structural and in vitro characterization of electrospun polylactic acid (PLA)/Chitosan nanofibers coated with cerium, copper or silver doped bioactive glasses (CeBG/CuBG/AgBG). Bead-free, smooth surfaced nanofibers were successfully prepared by using electrospinning technique. The nanocomposite fibers were obtained using a facile dip-coating method, their antibacterial activities against E. coliE. coli (ATCC 25922 strains) were measured by the disk diffusion method after 24 h of incubation at 37 °C. CeBG and CuBG decorated PLA/Chitosan nanofibers did not develop an inhibition zone against the bacteria. On the other hand, nanofibers coated with AgBG developed an inhibition zone against the bacteria. The as-prepared nanocomposite fibers were immersed in SBF for 1, 3 and 7 days in Simulated Body Fluid (SBF) for evaluation of in vitro bioactivity. All samples induced the formation of crystallites with roughly ruffled morphology and the pores of fibers were covered with the extensive growth of crystallites. Energy Dispersive X-ray (EDX) composition analysis showed that the crystallites possessed Ca/P ratio close to 1.67, confirming the good in-vitro bioactivity of the fibers.

Design of carbon nanofiber embedded conducting epoxy resin

International Nuclear Information System (INIS)

Gantayat, Subhra; Sarkar, Niladri; Rout, Dibyaranjan; Swain, Sarat K.

2017-01-01

Acid treated carbon nanofiber (t-CNF) reinforced epoxy nanocomposites were fabricated by hand lay-up method with various wt % of t-CNF loadings. Pristine or unmodified carbon nano fibers (u-CNFs) were made compatible with epoxy matrix by means of mixed acid treatment. Fabricated nanocomposites were characterized with Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) study, scanning electron microscopy (SEM), transmission electron microscopy (TEM) and atomic force microscopy (AFM). Mechanical and thermal properties of the nanocomposites were measured as a function of t-CNF content. Effect of acid treated CNFs on to the mechanical properties of epoxy nanocomposites was justified by comparing the mechanical properties of epoxy/t-CNF and epoxy/u-CNF nanocomposites with same loading level. The electrical conductivity was achieved by epoxy resin with a threshold at 1 wt % of t-CNF. Substantial improvement in thermal, mechanical and electrical properties of the synthesized epoxy/t-CNF nanocomposites may be suitable for fabricating electronic devices. - Highlights: • Epoxy/t-CNF nanocomposites are characterized by XRD, FTIR, SEM, AFM and TEM. • Electrical conductivity was achieved by epoxy with a threshold at 1 wt% of t-CNF. • Tensile strength is enhanced by 40% due to dispersion of t-CNF. • Synthesized nanocomposites are suitable for fabricating electronic devises.

Design of carbon nanofiber embedded conducting epoxy resin

Energy Technology Data Exchange (ETDEWEB)

Gantayat, Subhra [Department of Chemistry, Veer Surendra Sai University of Technology, Burla, Sambalpur 768018, Odisha (India); School of Applied Sciences, KIIT University, Bhubaneswar 751024, Odisha (India); Sarkar, Niladri [Department of Chemistry, Veer Surendra Sai University of Technology, Burla, Sambalpur 768018, Odisha (India); Rout, Dibyaranjan [School of Applied Sciences, KIIT University, Bhubaneswar 751024, Odisha (India); Swain, Sarat K., E-mail: swainsk2@yahoo.co.in [Department of Chemistry, Veer Surendra Sai University of Technology, Burla, Sambalpur 768018, Odisha (India)

2017-01-15

Acid treated carbon nanofiber (t-CNF) reinforced epoxy nanocomposites were fabricated by hand lay-up method with various wt % of t-CNF loadings. Pristine or unmodified carbon nano fibers (u-CNFs) were made compatible with epoxy matrix by means of mixed acid treatment. Fabricated nanocomposites were characterized with Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) study, scanning electron microscopy (SEM), transmission electron microscopy (TEM) and atomic force microscopy (AFM). Mechanical and thermal properties of the nanocomposites were measured as a function of t-CNF content. Effect of acid treated CNFs on to the mechanical properties of epoxy nanocomposites was justified by comparing the mechanical properties of epoxy/t-CNF and epoxy/u-CNF nanocomposites with same loading level. The electrical conductivity was achieved by epoxy resin with a threshold at 1 wt % of t-CNF. Substantial improvement in thermal, mechanical and electrical properties of the synthesized epoxy/t-CNF nanocomposites may be suitable for fabricating electronic devices. - Highlights: • Epoxy/t-CNF nanocomposites are characterized by XRD, FTIR, SEM, AFM and TEM. • Electrical conductivity was achieved by epoxy with a threshold at 1 wt% of t-CNF. • Tensile strength is enhanced by 40% due to dispersion of t-CNF. • Synthesized nanocomposites are suitable for fabricating electronic devises.

Treated Carbon Nanofibers for Storing Energy in Aqueous KOH

Science.gov (United States)

Firsich, David W.

2004-01-01

A surface treatment has been found to enhance the performances of carbon nanofibers as electrode materials for electrochemical capacitors in which aqueous solutions of potassium hydroxide are used as the electrolytes. In the treatment, sulfonic acid groups are attached to edge plane sites on carbon atoms. The treatment is applicable to a variety of carbon nanofibers, including fibrils and both single- and multiple-wall nanotubes. The reason for choosing nanofibers over powders and other forms of carbon is that nanofibers offer greater power features. In previous research, it was found that the surface treatment of carbon nanofibers increased energy-storage densities in the presence of acid electrolytes. Now, it has been found that the same treatment increases energy-storage densities of carbon nanofibers in the presence of alkaline electrolytes when the carbon is paired with a NiOOH electrode. This beneficial effect varies depending on the variety of carbon substrate to which it is applied. It has been conjectured that the sulfonic acid groups, which exist in a deprotonated state in aqueous KOH solutions, undergo reversible electro-chemical reactions that are responsible for the observed increases in energystorage capacities. The increases can be considerable: For example, in one case, nanofibers exhibited a specific capacitance of 34 Farads per gram before treatment and 172 Farads per gram (an increase of about 400 percent) after treatment. The most promising application of this development appears to lie in hybrid capacitors, which are devices designed primarily for storing energy. These devices are designed to be capable of (1) discharge at rates greater than those of batteries and (2) storing energy at densities approaching those of batteries. A hybrid capacitor includes one electrode like that of a battery and one electrode like that of an electrochemical capacitor. For example, a hybrid capacitor could contain a potassium hydroxide solution as the electrolyte

Preparation of Ag/HBP/PAN Nanofiber Web and Its Antimicrobial and Filtration Property

Directory of Open Access Journals (Sweden)

Li-Rong Yao

2016-01-01

Full Text Available To widen the application of nanofibers web in the field of medical health materials, a new Ag/amino-terminated hyperbranched polymer (HBP/polyacrylonitrile (PAN nanofiber web with excellent antimicrobial activity and filtration property was produced with Ag/HBP dispersion solution and PAN nanofiber. Ag/HBP dispersion solution was prepared with HBP as reducer and stabilizer, and Ag/HBP/PAN nanofiber was prepared by modifying electrospun PAN nanofiber with Ag/HBP aqueous solution. The characterization results showed that spherical Ag nanoparticles were prepared and they had a narrow distribution in HBP aqueous solution. The results of Ag/HBP/PAN nanofiber characterized with SEM and EDS showed that the content of silver nanoparticles on the surface of PAN nanofiber was on the increase when the treating temperature rose. The bacterial reduction rates of HBP-treated PAN nanofiber against S. aureus and E. coli were about 89%, while those of the Ag/HBP/PAN nanofiber against S. aureus and E. coli were 99.9% and 99.96%, respectively, due to the cooperative effects from the amino groups in HBP and Ag nanoparticles. Moreover, the small pores and high porosity in Ag/HBP/PAN nanofiber web resulted in high filtration efficiency (99.9% for removing smaller particles (0.1 μm~0.7 μm, which was much higher than that of the gauze mask.

Lysozyme-immobilized electrospun PAMA/PVA and PSSA-MA/PVA ion-exchange nanofiber for wound healing.

Science.gov (United States)

Tonglairoum, Prasopchai; Ngawhirunpat, Tanasait; Rojanarata, Theerasak; Opanasopit, Praneet

2014-08-27

Abstract This research was aimed to develop the lysozyme immobilized ion-exchange nanofiber mats for wound healing. To promote the healing process, the PSSA-MA/PVA and PAMA ion-exchange nanofiber mats were fabricated to mimic the extracellular matrix structure using electrospinning process followed by thermally crosslinked. Lysozyme was immobilized on the ion-exchane nanofibers by an adsorption method. The ion-exchange nanofibers were investigated using SEM, FTIR and XRPD. Moreover, the lysozyme-immobilized ion-exchange nanofibers were further investigated for lysozyme content and activity, lysozyme release and wound healing activity. The fiber diameters of the mats were in the nanometer range. Lysozyme was gradually absorbed into the PSSA-MA/PVA nanofiber with higher extend than that is absorbed on the PAMA/PVA nanofiber and exhibited higher activity than lysozyme-immobilized PAMA/PVA nanofiber. The total contents of lysozyme on the PSSA-MA/PVA and PAMA/PVA nanofiber were 648 and 166 µg/g, respectively. FTIR and lysozyme activity results confirmed the presence of lysozyme on the nanofiber mats. The lysozyme was released from the PSSA-MA/PVA and PAMA/PVA nanofiber in the same manner. The lysozyme-immobilized PSSA-MA/PVA nanofiber mats and lysozyme-immobilized PAMA/PVA nanofiber mats exhibited significantly faster healing rate than gauze and similar to the commercial antibacterial gauze dressing. These results suggest that these nanofiber mats could provide the promising candidate for wound healing application.

Electrospun polyacrylonitrile nanofibers loaded with silver nanoparticles by silver mirror reaction

International Nuclear Information System (INIS)

Shi, Yongzheng; Li, Yajing; Zhang, Jianfeng; Yu, Zhongzhen; Yang, Dongzhi

2015-01-01

The silver mirror reaction (SMR) method was selected in this paper to modify electrospun polyacrylonitrile (PAN) nanofibers, and these nanofibers loaded with silver nanoparticles showed excellent antibacterial properties. PAN nanofibers were first pretreated in AgNO 3 aqueous solution before the SMR process so that the silver nanoparticles were distributed evenly on the outer surface of the nanofibers. The final PAN nanofibers were characterized by scanning electron microscopy (SEM), energy dispersive spectrometer (EDS), transmission electron microscopy (TEM), TEM-selected area electron diffraction (SAED), X-ray diffraction (XRD) and thermogravimetric analysis (TGA). SEM, TEM micrographs and SAED patterns confirmed homogeneous dispersion of the silver nanoparticles which were composed of monocrystals with diameters 20–30 nm. EDS and XRD results showed that these monocrystals tended to form face-centered cubic single silver. TGA test indicated that the nanoparticles loaded on the nanofibers reached above 50 wt.%. This material was also evaluated by the viable cell-counting method. The results indicated that PAN nanofibers loaded with silver nanoparticles exhibited excellent antimicrobial activities against gram-negative Escherichia coli (E. coli), gram-positive Staphylococcus aureus (S. aureus) and the fungus Monilia albicans. Thus, this material had many potential applications in biomedical fields. - Highlights: • Silver mirror reaction was used to prepare nanofibers loaded with silver nanoparticles. • The SAED patterns demonstrated the monocrystallinity of silver nanocrystals. • The XRD results showed nanoparticles tended to be face-centered cubic single silver. • The material showed excellent antimicrobial activities against bacteria and fungi

Polyelectrolyte-Functionalized Nanofiber Mats Control the Collection and Inactivation of Escherichia coli

Directory of Open Access Journals (Sweden)

Katrina A. Rieger

2016-04-01

Full Text Available Quantifying the effect that nanofiber mat chemistry and hydrophilicity have on microorganism collection and inactivation is critical in biomedical applications. In this study, the collection and inactivation of Escherichia coli K12 was examined using cellulose nanofiber mats that were surface-functionalized using three polyelectrolytes: poly (acrylic acid (PAA, chitosan (CS, and polydiallyldimethylammonium chloride (pDADMAC. The polyelectrolyte functionalized nanofiber mats retained the cylindrical morphology and average fiber diameter (~0.84 µm of the underlying cellulose nanofibers. X-ray photoelectron spectroscopy (XPS and contact angle measurements confirmed the presence of polycations or polyanions on the surface of the nanofiber mats. Both the control cellulose and pDADMAC-functionalized nanofiber mats exhibited a high collection of E. coli K12, which suggests that mat hydrophilicity may play a larger role than surface charge on cell collection. While the minimum concentration of polycations needed to inhibit E. coli K12 was 800 µg/mL for both CS and pDADMAC, once immobilized, pDADMAC-functionalized nanofiber mats exhibited a higher inactivation of E. coli K12, (~97%. Here, we demonstrate that the collection and inactivation of microorganisms by electrospun cellulose nanofiber mats can be tailored through a facile polyelectrolyte functionalization process.

Polyelectrolyte-Functionalized Nanofiber Mats Control the Collection and Inactivation of Escherichia coli

Science.gov (United States)

Rieger, Katrina A.; Porter, Michael; Schiffman, Jessica D.

2016-01-01

Quantifying the effect that nanofiber mat chemistry and hydrophilicity have on microorganism collection and inactivation is critical in biomedical applications. In this study, the collection and inactivation of Escherichia coli K12 was examined using cellulose nanofiber mats that were surface-functionalized using three polyelectrolytes: poly (acrylic acid) (PAA), chitosan (CS), and polydiallyldimethylammonium chloride (pDADMAC). The polyelectrolyte functionalized nanofiber mats retained the cylindrical morphology and average fiber diameter (~0.84 µm) of the underlying cellulose nanofibers. X-ray photoelectron spectroscopy (XPS) and contact angle measurements confirmed the presence of polycations or polyanions on the surface of the nanofiber mats. Both the control cellulose and pDADMAC-functionalized nanofiber mats exhibited a high collection of E. coli K12, which suggests that mat hydrophilicity may play a larger role than surface charge on cell collection. While the minimum concentration of polycations needed to inhibit E. coli K12 was 800 µg/mL for both CS and pDADMAC, once immobilized, pDADMAC-functionalized nanofiber mats exhibited a higher inactivation of E. coli K12, (~97%). Here, we demonstrate that the collection and inactivation of microorganisms by electrospun cellulose nanofiber mats can be tailored through a facile polyelectrolyte functionalization process. PMID:28773422

Fabrication and Characterization of Electrospun Wool Keratin/Poly(vinyl alcohol Blend Nanofibers

Directory of Open Access Journals (Sweden)

Shuai Li

2014-01-01

Full Text Available Wool keratin/poly(vinyl alcohol (PVA blend nanofibers were fabricated using the electrospinning method in formic acid solutions with different weight ratios of keratin to PVA. The resultant blend nanofibers were characterized by scanning electron microscopy (SEM, Fourier transform infrared (FTIR, X-ray diffraction (XRD, thermal gravimetric analysis (TGA, and tensile test. SEM images showed that the diameter of the blend nanofibers was affected by the content of keratin in blend solution. FTIR and XRD analyses data demonstrated that there were good interactions between keratin and PVA in the blended nanofibers caused by possibly hydrogen bonds. The TGA study revealed that the thermal stability of the blend nanofibers was between those of keratin and PVA. Tensile test indicated that the addition of PVA was able to improve the mechanical properties of the electrospun nanofibers.

Neurotensin-loaded PLGA/CNC composite nanofiber membranes accelerate diabetic wound healing.

Science.gov (United States)

Zheng, Zhifang; Liu, Yishu; Huang, Wenhua; Mo, Yunfei; Lan, Yong; Guo, Rui; Cheng, Biao

2018-04-13

Diabetic foot ulcers (DFUs) are a threat to human health and can lead to amputation and even death. Recently neurotensin (NT), an inflammatory modulator in wound healing, was found to be beneficial for diabetic wound healing. As we demonstrated previously, polylactide-polyglycolide (PLGA) and cellulose nanocrystals (CNCs) (PLGA/CNC) nanofiber membranes show good cytocompatibility and facilitate fibroblast adhesion, spreading and proliferation. PLGA/CNC nanofiber membranes are novel materials that have not been used previously as NT carriers in diabetic wounds. This study aims to explore the therapeutic efficacy and possible mechanisms of NT-loaded PLGA/CNC nanofiber membranes in full-thickness skin wounds in spontaneously diabetic mice. The results showed that NT could be sustained released from NT-loaded PLGA/CNC composite nanofiber membranes for 2 weeks. NT-loaded PLGA/CNC composite nanofiber membranes induced more rapid healing than other control groups. After NT exposure, the histological scores of the epidermal and dermal regeneration and the ratios of the fibrotic area to the whole area were increased. NT-loaded PLGA/CNC composite nanofiber membranes also decreased the expressions of the inflammatory cytokines IL-1β and IL-6. These results suggest that NT-loaded PLGA/CNC composite nanofiber membranes for sustained delivery of NT should effectively promote tissue regeneration for the treatment of DFUs.

Electrospun polyacrylonitrile nanofibers functionalized with EDTA for adsorption of ionic dyes

Science.gov (United States)

Chaúque, Eutilério F. C.; Dlamini, Langelihle N.; Adelodun, Adedeji A.; Greyling, Corinne J.; Ngila, J. Catherine

2017-08-01

The manipulation of nanofibers' surface chemistry could enhance their potential application toward the removal of ionic dyes in wastewater. For this purpose, surface modification of electrospun polyacrylonitrile (PAN) nanofibers with ethylenediaminetetraacetic acid (EDTA) and ethylenediamine (EDA) crosslinker was experimented. The functionalized EDTA-EDA-PAN nanofibers were characterized using Fourier transform infrared (FT-IR) spectroscopy, X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and Brunauer-Emmett-Teller (BET) technique. The impregnation of EDA and EDTA chelating agents on the surface of PAN changed the distribution of nanofibers as proximity is increased (accompanied by reduced softness), but the nanofibrous structure of the pristine PAN nanofibers was not substantially altered. Adsorption equilibrium studies were performed with Freundlich, Langmuir and Temkin isotherm models with the former providing better correlation to the experimental data. The modified PAN nanofibers showed efficient sorption of methyl orange (MO) and reactive red (RR) from aqueous synthetic samples, evinced by the maximum adsorption capacities (at 25 °C) of 99.15 and 110.0 mg g-1, respectively. The fabricated nanofibers showed appreciable removal efficiency of the target dye sorptives from wastewater. However, the presence of high metal ions content affected the overall extraction of dyes from wastewater due to the depletion of the adsorbent's active adsorptive sites.

Surface structure enhanced second harmonic generation in organic nanofibers

DEFF Research Database (Denmark)

Fiutowski, Jacek; Maibohm, Christian; Kostiučenko, Oksana

Second-harmonic generation upon femto-second laser irradiation of nonlinearly optically active nanofibers grown from nonsymmetrically functionalized para-quarterphenylene (CNHP4) molecules is investigated. Following growth on mica templates, the nanofibers have been transferred onto lithography...

Piezoelectric properties of electrospun nanofibers of BaTiO3

International Nuclear Information System (INIS)

Carvalho, L.F.R.M.; Melo, G.F.; Goncalves, A.M.; Eiras, J.A.; Bretas, R.E.S.

2016-01-01

BaTiO3 nanofibers were produced by the electrospinning method from a mixture of a solution of the precursors Ba (CH_3COO)_2 and [(CH_3)_2CHO]_4Ti in acetic acid and a solution of poly(vinylpyrrolidone) in ethanol. A voltage of 10 kV and a working distance of 4.6 cm were used for the electrospinning, at controlled room temperature and humidity of 21 °C and 60% respectively. Nanofibers as spun were dried in air on an air-circulating oven at 100 °C for one hour to remove residual solvent and were subsequently calcined at 750 °C during 2 h. The morphology, crystallographic structure and piezoelectric properties of the nanofibers were analyzed by scanning electron microscopy (SEM), X-ray angle (WAXS) and Piezoresponse Force Microscopy (PFM), respectively. The average diameter of the nanofibers was 414 nm with an aspect ratio of 40. By PFM, there was strong evidence that the nanofibers had piezoelectric activity. (author)

Improved fire retardancy of thermoset composites modified with carbon nanofibers

International Nuclear Information System (INIS)

Zhao Zhongfu; Gou Jan

2009-01-01

Multifunctional thermoset composites were made from polyester resin, glass fiber mats and carbon nanofiber sheets (CNS). Their flaming behavior was investigated with cone calorimeter under well-controlled combustion conditions. The heat release rate was lowered by pre-planting carbon nanofiber sheets on the sample surface with the total fiber content of only 0.38 wt.%. Electron microscopy showed that carbon nanofiber sheet was partly burned and charred materials were formed on the combusting surface. Both the nanofibers and charred materials acted as an excellent insulator and/or mass transport barrier, improving the fire retardancy of the composite. This behavior agrees well with the general mechanism of fire retardancy in various nanoparticle-thermoplastic composites.

Stability of β-carotene in polyethylene oxide electrospun nanofibers

Energy Technology Data Exchange (ETDEWEB)

Peinado, I., E-mail: irpeipar@upvnet.upv.es [Free University of Bolzano, Piazza Università 5, 39100 Bolzano (Italy); Mason, M.; Romano, A. [Free University of Bolzano, Piazza Università 5, 39100 Bolzano (Italy); Biasioli, F. [Department of Food Quality and Nutrition, Research and Innovation Centre, Fondazione Edmund Mach (FEM), via E. Mach 1, 38010 San Michele all ‘Adige, TN (Italy); Scampicchio, M., E-mail: matteo.scampicchio@unibz.it [Free University of Bolzano, Piazza Università 5, 39100 Bolzano (Italy)

2016-05-01

Highlights: • β-carotene was incorporated into PEO-nanofibers by electrospinning. • Properties of the fibers were analyzed by SEM, color analysis, and DSC. • TGA coupled to PTR–ms resulted promising to online-monitoring thermal degradation. • Thermal stability of βc increased after encapsulation into the PEO-nanofibers. - Abstract: β-carotene (βc) was successfully incorporated into electrospun nanofibers of poly-(ethylene oxide) (PEO) with the aim of prolonging its shelf life and thermal stability. The physical and thermal properties of the βc-PEO-nanofibers were determined by scanning electron microscopy (SEM), color analysis, and differential scanning calorimetry (DSC). The nanofibers of PEO and βc-PEO exhibited average fiber diameters of 320 ± 46 and 230 ± 21 nm, with colorimetric coordinates L* = 95.7 ± 2.4 and 89.4 ± 4.6 and b* = −0.5 ± 0.1 and 6.2 ± 3.0 respectively. Thermogravimetric analysis coupled with Proton Transfer–Mass Spectroscopy (TGA/PTR–ms) demonstrated that coated βc inside PEO nanofibers increased thermal stability when compared to standard βc in powder form. In addition, β-carotene in the membranes showed higher stability during storage when compared with β-carotene in solution with a decrease in concentration of 57 ± 4% and 70 ± 2% respectively, thus should extend the shelf life of this compound. Also, TGA coupled with PTR–MS resulted in a promising technique to online-monitoring thermal degradation.

Preparation and characterization of single-crystal multiferroic nanofiber composites

Energy Technology Data Exchange (ETDEWEB)

Ren, Zhaohui; Xiao, Zhen; Yin, Simin; Mai, Jiangquan; Liu, Zhenya; Xu, Gang; Li, Xiang; Shen, Ge [State Key Lab of Silicon Materials, Department of Material Science and Engineering, Cyrus Tang Center for Sensor Materials and Applications, Zhejiang University, Hangzhou 310027 (China); Han, Gaorong, E-mail: hgr@zju.edu.cn [State Key Lab of Silicon Materials, Department of Material Science and Engineering, Cyrus Tang Center for Sensor Materials and Applications, Zhejiang University, Hangzhou 310027 (China)

2013-03-05

Graphical abstract: One-dimensional single-crystal multiferroic composites composed of PbTiO{sub 3} nanofiber-CoFe{sub 2}O{sub 4} nanodot have been prepared for the first time by a facile in situ solid state sintering method. The composites demonstrate ferroelectricity and ferromagnetism as well as strong coupling between them. Highlights: ► 1D single-crystal multiferroic PTO-CFO was prepared via in situ solid state sintering method. ► A simple epitaxial growth relation has been found between the PTO–CFO composites. ► The composites reveal ferroelectricity and ferromagnetism as well as coupling between them. -- Abstract: One-dimensional single-crystal multiferroic composites consisting of PbTiO{sub 3} (PTO) nanofiber-CoFe{sub 2}O{sub 4} (CFO) nanodot were prepared using an in situ solid state sintering method, where pre-perovskite PTO nanofibers and CFO nanodots were used as precursors. Structural analyses by using transmission electron microscopy, scanning electron microscopy and X-ray diffraction determined a epitaxial growth relation between the PTO nanofiber and the CFO nanodot. Ferromagnetism and ferroelectricity of the nanofiber composites were investigated by using vibarting sample magnetometer (VSM) and piezoresponse force microscopy (PFM)

Fabrication and application of coaxial polyvinyl alcohol/chitosan nanofiber membranes

Directory of Open Access Journals (Sweden)

Kuo Ting-Yun

2017-12-01

Full Text Available It is difficult to fabricate chitosan-wrapped coaxial nanofibers, because highly viscous chitosan solutions might hinder the manufacturing process. To overcome this difficulty, our newly developed method, which included the addition of a small amount of gum arabic, was utilized to prepare much less viscous chitosan solutions. In this way, coaxial polyvinyl alcohol (PVA/chitosan (as core/shell nanofiber membranes were fabricated successfully by coaxial electrospinning. The core/shell structures were confirmed by TEM, and the existence of PVA and chitosan was also verified using FT-IR and TGA. The tensile strength of the nanofiber membranes was increased from 0.6-0.7 MPa to 0.8-0.9 MPa after being crosslinked with glutaraldehyde. The application potential of the PVA/chitosan nanofiber membranes was tested in drug release experiments by loading the core (PVA with theophylline as a model drug. The use of the coaxial PVA/chitosan nanofiber membranes in drug release extended the release time of theophylline from 5 minutes to 24 hours. Further, the release mechanisms could be described by the Korsmeyer-Peppas model. In summary, by combining the advantages of PVA and chitosan (good mechanical strength and good biocompatibility respectively, the coaxial PVA/chitosan nanofiber membranes are potential biomaterials for various biomedical applications.

Preparation of Diethylenetriamine Modified Polyacrylonitrile Nanofibers for Cadmium Ion Adsorption

Directory of Open Access Journals (Sweden)

Zahra Mokhtari- shorijeh

2016-07-01

Full Text Available In this study, the electrospinning method was used to manufacture polyacrylonitrile (PAN nanofibers. The procedure involved spinning a solution of 10%wt PAN in dimethyl formamide (DMF in an electric field of 21 kV and with a tip to collector distance of 16 cm. The nanofibers thus obtained had an average diameter of 100 nm. Then, scanning electron microscopy (SEM images were used to investigate the morphology of the nanofibers. In the next step, the nanofiner surface was modified with diethylenetriamine and FTIR was employed to ensure the presence of amines on the nanofiber surface. The functionalized nanofibers were then used for the first time to adsorb ions of cadmium (a heavy metal with industrial applications and its adsorption capacity was evaluated. The chemical charactristics of the nanofibers and the effects of such parameters as pH, temprature, and contact time on adsorption efficiency were investigated. The results showed that maximum adsorption efficiency was achieved within the first 10 minutes of the process at a pH in the range of 5‒7 when about 80% of the cadmium ions were adsorbed.. Moreover, only slight changes were observed with longer contact times or with increasing temperature. Finally, the adsorption data fitted well with the Langmuir isotherm

Superhydrophilicity of a nanofiber-covered aluminum surface fabricated via pyrophosphoric acid anodizing

Science.gov (United States)

Nakajima, Daiki; Kikuchi, Tatsuya; Natsui, Shungo; Suzuki, Ryosuke O.

2016-12-01

A superhydrophilic aluminum surface covered by numerous alumina nanofibers was fabricated via pyrophosphoric acid anodizing. High-density anodic alumina nanofibers grow on the bottom of a honeycomb oxide via anodizing in concentrated pyrophosphoric acid. The water contact angle on the nanofiber-covered aluminum surface decreased with time after a 4 μL droplet was placed on the surface, and a superhydrophilic behavior with a contact angle measuring 2.2° was observed within 2 s; this contact angle is considerably lower than those observed for electropolished and porous alumina-covered aluminum surfaces. There was no dependence of the superhydrophilicity on the density of alumina nanofibers fabricated via different constant voltage anodizing conditions. The superhydrophilic property of the surface covered by anodic alumina nanofibers was maintained during an exposure test for 359 h. The quick-drying and snow-sliding behaviors of the superhydrophilic aluminum covered with anodic alumina nanofibers were demonstrated.

Electrospun polyacrylonitrile nanofibers loaded with silver nanoparticles by silver mirror reaction

Energy Technology Data Exchange (ETDEWEB)

Shi, Yongzheng; Li, Yajing; Zhang, Jianfeng; Yu, Zhongzhen; Yang, Dongzhi, E-mail: yangdz@mail.buct.edu.cn

2015-06-01

The silver mirror reaction (SMR) method was selected in this paper to modify electrospun polyacrylonitrile (PAN) nanofibers, and these nanofibers loaded with silver nanoparticles showed excellent antibacterial properties. PAN nanofibers were first pretreated in AgNO{sub 3} aqueous solution before the SMR process so that the silver nanoparticles were distributed evenly on the outer surface of the nanofibers. The final PAN nanofibers were characterized by scanning electron microscopy (SEM), energy dispersive spectrometer (EDS), transmission electron microscopy (TEM), TEM-selected area electron diffraction (SAED), X-ray diffraction (XRD) and thermogravimetric analysis (TGA). SEM, TEM micrographs and SAED patterns confirmed homogeneous dispersion of the silver nanoparticles which were composed of monocrystals with diameters 20–30 nm. EDS and XRD results showed that these monocrystals tended to form face-centered cubic single silver. TGA test indicated that the nanoparticles loaded on the nanofibers reached above 50 wt.%. This material was also evaluated by the viable cell-counting method. The results indicated that PAN nanofibers loaded with silver nanoparticles exhibited excellent antimicrobial activities against gram-negative Escherichia coli (E. coli), gram-positive Staphylococcus aureus (S. aureus) and the fungus Monilia albicans. Thus, this material had many potential applications in biomedical fields. - Highlights: • Silver mirror reaction was used to prepare nanofibers loaded with silver nanoparticles. • The SAED patterns demonstrated the monocrystallinity of silver nanocrystals. • The XRD results showed nanoparticles tended to be face-centered cubic single silver. • The material showed excellent antimicrobial activities against bacteria and fungi.

Growth and Integration of Organic Nanofibers in Devices

DEFF Research Database (Denmark)

Thilsing-Hansen, Kasper

kæder af krystalliter, der tilslutter sig den allerede eksisterende P6P nanofiber. Overførsel af P6P nanofibre fra deres vækst substrat er uundgåeligt for at implementere p6P nanofibre i komponenter. Kontrolleret overførsel af 200x200μm2 nanofiber områder fra vækst substratet til præfabrikerede silicium......) exciteret med en pulserende laserstråle et guld/vakuum interface, hvilket resulterer i nanofiber lokaliseret mønstre i PEEM billederne....

Local field enhanced second-harmonic response of organic nanofibers

DEFF Research Database (Denmark)

Leißner, Till; Kostiučenko, Oksana; Fiutowski, Jacek

Organic CNHP4 nanofibers showing a strong second-harmonic (SH) response have been successfully implemented as active components in a metal-organic hybrid system. Using nondestructive roll-on transfer technique nanofibers were transferred from the growing mica substrates onto electron...

Design and Characterization of Electrospun Polyamide Nanofiber Media for Air Filtration Applications

Directory of Open Access Journals (Sweden)

Jonas Matulevicius

2014-01-01

Full Text Available Electrospun polyamide 6 (PA 6 and polyamide 6/6 (PA 6/6 nanofibers were produced in order to investigate their experimental characteristics with the goal of obtaining filtration relevant fiber media. The experimental design model of each PA nanofibers contained the following variables: polymer concentration, ratio of solvents, nanofiber media collection time, tip-to-collector distance, and the deposition voltage. The average diameter of the fibers, their morphology, basis weight, thickness, and resulting media solidity were investigated. Effects of each variable on the essential characteristics of PA 6/6 and PA 6 nanofiber media were studied. The comparative analysis of the obtained PA 6/6 and PA 6 nanofiber characteristics revealed that PA 6/6 had higher potential to be used in filtration applications. Based on the experimental results, the graphical representation—response surfaces—for obtaining nanofiber media with the desirable fiber diameter and basis weight characteristics were derived. Based on the modelling results the nanofiber filter media (mats were fabricated. Filtration results revealed that nanofiber filter media electrospun from PA6/6 8% (w/vol solutions with the smallest fiber diameters (62–66 nm had the highest filtration efficiency (PA6/6_30 = 84.9–90.9% and the highest quality factor (PA6/6_10 = 0.0486–0.0749 Pa−1.

High-Temperature Stable Anatase Titanium Oxide Nanofibers for Lithium-Ion Battery Anodes.

Science.gov (United States)

Lee, Sangkyu; Eom, Wonsik; Park, Hun; Han, Tae Hee

2017-08-02

Control of the crystal structure of electrochemically active materials is an important approach to fabricating high-performance electrodes for lithium-ion batteries (LIBs). Here, we report a methodology for controlling the crystal structure of TiO 2 nanofibers by adding aluminum isopropoxide to a common sol-gel precursor solution utilized to create TiO 2 nanofibers. The introduction of aluminum cations impedes the phase transformation of electrospun TiO 2 nanofibers from the anatase to the rutile phase, which inevitably occurs in the typical annealing process utilized for the formation of TiO 2 crystals. As a result, high-temperature stable anatase TiO 2 nanofibers were created in which the crystal structure was well-maintained even at high annealing temperatures of up to 700 °C. Finally, the resulting anatase TiO 2 nanofibers were utilized to prepare LIB anodes, and their electrochemical performance was compared to pristine TiO 2 nanofibers that contain both anatase and rutile phases. Compared to the electrode prepared with pristine TiO 2 nanofibers, the electrode prepared with anatase TiO 2 nanofibers exhibited excellent electrochemical performances such as an initial Coulombic efficiency of 83.9%, a capacity retention of 89.5% after 100 cycles, and a rate capability of 48.5% at a current density of 10 C (1 C = 200 mA g -1 ).

Electrospun polyvinylpyrrolidone (PVP)/green tea extract composite nanofiber mats and their antioxidant activities

Science.gov (United States)

Pusporini, Pusporini; Edikresnha, Dhewa; Sriyanti, Ida; Suciati, Tri; Miftahul Munir, Muhammad; Khairurrijal, Khairurrijal

2018-05-01

Electrospinning was employed to make PVP (polyvinylpyrrolidone)/GTE (green tea extract) composite nanofiber mats. The electrospun PVP nanofiber mat as well as the PVP/GTE nanofiber mats were uniform. The average fiber diameter of PVP/GTE composite nanofiber mat decreased with increasing the GTE weight fraction (or decreasing the PVP weight fraction) in the PVP/GTE solution because the PVP/GTE solution concentration decreased. Then, the broad FTIR peak representing the stretching vibrations of O–H in hydroxyl groups of phenols and the stretching of N–H in amine groups of the GTE paste shifted to higher wavenumbers in the PVP/GTE composite nanofiber mats. These peak shifts implied that PVP and catechins of GTE in the PVP/GTE composite nanofiber mats had intermolecular interactions via hydrogen bonds between carbonyl groups of PVP and hydroxyl groups of catechins in GTE. Lastly, the antioxidant activity of the PVP/GTE composite nanofiber mat increased with reducing the average fiber diameter because the amount of catechins in the composite nanofiber mat increased with the increase of surface area due to the reduction of the average fiber diameter.

Highly conductive electrospun carbon nanofiber/MnO2 coaxial nano-cables for high energy and power density supercapacitors

Science.gov (United States)

Zhi, Mingjia; Manivannan, Ayyakkannu; Meng, Fanke; Wu, Nianqiang

2012-06-01

This paper presents highly conductive carbon nanofiber/MnO2 coaxial cables in which individual electrospun carbon nanofibers are coated with an ultrathin hierarchical MnO2 layer. In the hierarchical MnO2 structure, an around 4 nm thick sheath surrounds the carbon nanofiber (CNF) in a diameter of 200 nm, and nano-whiskers grow radically outward from the sheath in view of the cross-section of the coaxial cables, giving a high specific surface area of MnO2. The CNFs are synthesized by electrospinning a precursor containing iron acetylacetonate (AAI). The addition of AAI not only enlarges the specific surface area of the CNF but also greatly enhances their electronic conductivity, which leads to a dramatic improvement in the specific capacitance and the rate capability of the CNF/MnO2 electrode. The AAI-CNF/MnO2 electrode shows a specific capacitance of 311 F g-1 for the whole electrode and 900 F g-1 for the MnO2 shell at a scan rate of 2 mV s-1. Good cycling stability, high energy density (80.2 Wh kg-1) and high power density (57.7 kW kg-1) are achieved. This work indicates that high electronic conductivity of the electrode material is crucial to achieving high power and energy density for pseudo-supercapacitors.

Piezoelectric and optoelectronic properties of electrospinning hybrid PVDF and ZnO nanofibers

Science.gov (United States)

Ma, Jian; Zhang, Qian; Lin, Kabin; Zhou, Lei; Ni, Zhonghua

2018-03-01

Polyvinylidene fluoride (PVDF) is a unique ferroelectric polymer with significant promise for energy harvesting, data storage, and sensing applications. ZnO is a wide direct band gap semiconductor (3.37 eV), commonly used as ultraviolet photodetectors, nanoelectronics, photonicsand piezoelectric generators. In this study, we produced high output piezoelectric energy harvesting materials using hybrid PVDF/ZnO nanofibers deposited via electrospinning. The strong electric fields and stretching forces during the electrospinning process helps to align dipoles in the nanofiber crystal such that the nonpolar α-phase (random orientation of dipoles) is transformed into polar β-phase in produced nanofibers. The effect of the additional ZnO nanowires on the nanofiber β-phase composition and output voltage are investigated. The maximum output voltage generated by a single hybrid PVDF and ZnO nanofiber (33 wt% ZnO nanowires) is over 300% of the voltage produced by a single nanofiber made of pure PVDF. The ZnO NWs served not only as a piezoelectric material, but also as a semiconducting material. The electrical conductivity of the hybrid PVDF/ZnO nanofibers increased by more than a factor of 4 when exposed under ultraviolet (UV) light.

Oxolane-2,5-dione modified electrospun cellulose nanofibers for heavy metals adsorption

International Nuclear Information System (INIS)

Stephen, Musyoka; Catherine, Ngila; Brenda, Moodley; Andrew, Kindness; Leslie, Petrik; Corrine, Greyling

2011-01-01

Highlights: → Electrospun and modified cellulose nanofibers have high surface area. → Modified nanofibers showed improved adsorption of Cd and Pb from water. → Regenerated modified nanofibers had high adsorption capacity hence recyclable. - Abstract: Functionalized cellulose nanofibers have been obtained through electrospinning and modification with oxolane-2,5-dione. The application of the nanofibers for adsorption of cadmium and lead ions from model wastewater samples is presented for the first time. Physical and chemical properties of the nanofibers were characterized. Surface chemistry during preparation and functionalization was monitored using Fourier transform-infrared spectroscopy, scanning electron microscopy, carbon-13 solid state nuclear magnetic resonance spectroscopy and Brunauer Emmett and Teller. Enhanced surface area of 13.68 m 2 g -1 was recorded for the nanofibers as compared to the cellulose fibers with a surface area of 3.22 m 2 g -1 . Freundlich isotherm was found to describe the interactions better than Langmuir: K f = 1.0 and 2.91 mmol g -1 (r 2 = 0.997 and 0.988) for lead and cadmium, respectively. Regenerability of the fiber mats was investigated and the results obtained indicate sustainability in adsorption efficacy of the material.

High temperature resistant nanofiber by bubbfil-spinning

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Li Ya

2015-01-01

Full Text Available Heat-resisting nanofibers have many potential applications in various industries, and the bubbfil spinning is the best candidate for mass-production of such materials. Polyether sulfone/zirconia solution with a bi-solvent system is used in the experiment. Experimental result reveals that polyether sulfone/zirconia nanofibers have higher resistance to high temperature than pure polyether sulfone fibers, and can be used as high-temperature-resistant filtration materials.

Morphology study of nanofibers produced by extraction from polymer blend fibers using image processing

International Nuclear Information System (INIS)

Dehghan, Neda; Tavanaie, Mohammad Ali; Payvandy, Pedram

2015-01-01

The morphology of nanofibers extracted from the industrial-scale produced polypropylene/polybutylene terephthalate (PP/PBT) blend fibers was studied. To study the morphology and diameter measurements of the nanofibers, image processing method was used, and the results were compared with the results of a conventional visual method. Comparing these two methods indicated the good performance of image processing methods for the measuring of nanofiber diameter. Among the various applied image processing methods, the fuzzy c-means (FCM) method was determined as the best for image thresholding. Additionally, the distance transform method was determined as the best way for measuring nanofiber diameter. According to high regression coefficient (R=0.98) resulting between the draw ratio and nanofibers diameter, the high effectiveness of draw ratio to nanofiber diameter is concluded. The spherical (drop) shapes of the PBT dispersed phase particles were eventually deformed into very thin fibrils during the drawing process. The results of measuring the nanofiber diameters showed that the diameter means of nanofibers varied from 420 nm to 175 nm with the highest draw ratio. Good uniformity for diameter of nanofibers was observed, which had not been observed in previous works.

Morphology study of nanofibers produced by extraction from polymer blend fibers using image processing

Energy Technology Data Exchange (ETDEWEB)

Dehghan, Neda; Tavanaie, Mohammad Ali; Payvandy, Pedram [University of Yazd, Yazd (Iran, Islamic Republic of)

2015-09-15

The morphology of nanofibers extracted from the industrial-scale produced polypropylene/polybutylene terephthalate (PP/PBT) blend fibers was studied. To study the morphology and diameter measurements of the nanofibers, image processing method was used, and the results were compared with the results of a conventional visual method. Comparing these two methods indicated the good performance of image processing methods for the measuring of nanofiber diameter. Among the various applied image processing methods, the fuzzy c-means (FCM) method was determined as the best for image thresholding. Additionally, the distance transform method was determined as the best way for measuring nanofiber diameter. According to high regression coefficient (R=0.98) resulting between the draw ratio and nanofibers diameter, the high effectiveness of draw ratio to nanofiber diameter is concluded. The spherical (drop) shapes of the PBT dispersed phase particles were eventually deformed into very thin fibrils during the drawing process. The results of measuring the nanofiber diameters showed that the diameter means of nanofibers varied from 420 nm to 175 nm with the highest draw ratio. Good uniformity for diameter of nanofibers was observed, which had not been observed in previous works.

Carbon Nanofibers Synthesized on Selective Substrates for Nonvolatile Memory and 3D Electronics

Science.gov (United States)

Kaul, Anupama B.; Khan, Abdur R.

2011-01-01

A plasma-enhanced chemical vapor deposition (PECVD) growth technique has been developed where the choice of starting substrate was found to influence the electrical characteristics of the resulting carbon nanofiber (CNF) tubes. It has been determined that, if the tubes are grown on refractory metallic nitride substrates, then the resulting tubes formed with dc PECVD are also electrically conducting. Individual CNFs were formed by first patterning Ni catalyst islands using ebeam evaporation and liftoff. The CNFs were then synthesized using dc PECVD with C2H2:NH3 = [1:4] at 5 Torr and 700 C, and approximately equal to 200-W plasma power. Tubes were grown directly on degenerately doped silicon substrates with resistivity rho approximately equal to 1-5 meterohm-centimeter, as well as NbTiN. The approximately equal to 200-nanometer thick refractory NbTiN deposited using magnetron sputtering had rho approximately equal to 113 microohm-centimeter and was also chemically compatible with CNF synthesis. The sample was then mounted on a 45 beveled Al holder, and placed inside a SEM (scanning electron microscope). A nanomanipulator probe stage was placed inside the SEM equipped with an electrical feed-through, where tungsten probes were used to make two-terminal electrical measurements with an HP 4156C parameter analyzer. The positive terminal nanoprobe was mechanically manipulated to physically contact an individual CNF grown directly on NbTiN as shown by the SEM image in the inset of figure (a), while the negative terminal was grounded to the substrate. This revealed the tube was electrically conductive, although measureable currents could not be detected until approximately equal to 6 V, after which point current increased sharply until compliance (approximately equal to 50 nA) was reached at approximately equal to 9.5 V. A native oxide on the tungsten probe tips may contribute to a tunnel barrier, which could be the reason for the suppressed transport at low biases

Catalytic Growth of Macroscopic Carbon Nanofibers Bodies with Activated Carbon

Science.gov (United States)

Abdullah, N.; Rinaldi, A.; Muhammad, I. S.; Hamid, S. B. Abd.; Su, D. S.; Schlogl, R.

2009-06-01

Carbon-carbon composite of activated carbon and carbon nanofibers have been synthesized by growing Carbon nanofiber (CNF) on Palm shell-based Activated carbon (AC) with Ni catalyst. The composites are in an agglomerated shape due to the entanglement of the defective CNF between the AC particles forming a macroscopic body. The macroscopic size will allow the composite to be used as a stabile catalyst support and liquid adsorbent. The preparation of CNT/AC nanocarbon was initiated by pre-treating the activated carbon with nitric acid, followed by impregnation of 1 wt% loading of nickel (II) nitrate solutions in acetone. The catalyst precursor was calcined and reduced at 300° C for an hour in each step. The catalytic growth of nanocarbon in C2H4/H2 was carried out at temperature of 550° C for 2 hrs with different rotating angle in the fluidization system. SEM and N2 isotherms show the level of agglomeration which is a function of growth density and fluidization of the system. The effect of fluidization by rotating the reactor during growth with different speed give a significant impact on the agglomeration of the final CNF/AC composite and thus the amount of CNFs produced. The macrostructure body produced in this work of CNF/AC composite will have advantages in the adsorbent and catalyst support application, due to the mechanical and chemical properties of the material.

A nanofiber functionalized with dithizone by co-electrospinning for lead (II) adsorption from aqueous media

International Nuclear Information System (INIS)

Deng, Jianjun; Kang, Xuejun; Chen, Liqin; Wang, Yu; Gu, Zhongze; Lu, Zuhong

2011-01-01

Highlights: ► We fabricated a composite electrospun nanofiber as a selective sorbent for lead (II) in PFSPE. ► The composite nanofiber was functionalized with the dithizone by co-electrospinning of the PS solution containing unbonded dithizone. ► The nanofiber was characterized by scanning electron microscope and IR spectra. ► We applied the nanofiber by packing in a cartridge. ► The nanofiber performed well in the absorption of lead (II) and was applied successfully in aqueous samples. - Abstract: An electrospun nanofiber was utilized as a sorbent in packed fiber solid phase extraction (PFSPE) for selective separation and preconcentration of lead (II). The nanofiber had a polystyrene (PS) backbone, which was functionalized with dithizone (DZ) by co-electrospinning of a PS solution containing DZ. The nanofiber exhibited its performance in a cartridge prepared by packing 5 mg of nanofiber. The nanofiber was characterized by a scanning electron microscope and IR spectra. The diameter of the nanofiber was less than 400 nm. After being activated by 2.0 mol L −1 NaOH aqueous solution, the nanofiber quantitatively sorbed lead (II) at pH 8.5, and the metal ion could be desorbed from it by three times of elution with a small volume of 0.1 mol L −1 HNO 3 aqueous solution. The breakthrough capacity was 16 μg mg −1 . The nanofiber could be used for concentration of lead (II) from water and other aqueous media, such as plasma with stable recovery in a simple and convenient manner.

Preparation of Biopolymeric Nanofiber Containing Silica and Antibiotic

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A. Bagheri Pebdeni

2016-01-01

Full Text Available The biocompatible and biodegradable polymer nanofiber with high potential for anti-bacterial coating are used for: multi-functional membranes, tissue engineering, wound dressings, drug delivery, artificial organs, vascular grafts and etc. Electrospinning nanofiber made of scaffolding due to characteristics such as high surface to volume ratio, high porosity and very fine pores are used for a wide range of applications. In this study, polymer composite nanofiber Silica/chitosan/poly (ethylene oxide /cefepime antibiotic synthesis and antibacterial properties will be discussed. The optimum conditions for preparation of electrospun nanofiber were: voltage; 21 kV, feed rate; 0.5 mL/h, nozzle-collector distance; 10 cm, and chitosan/poly(ethylene oxide weight ratio 90:10 and the volume ratio of chitosan/silica is 70:30.  The antibacterial activity of composite scaffolds were tested by agar plate method by two type bacteria including Escherichia coli and Staphylococcus aureus. With the addition of the silica to chitosan, the hybrid was more biodegradable and improves the mechanical properties of biopolymer.

Electrospinning of functional poly(methyl methacrylate) nanofibers containing cyclodextrin-menthol inclusion complexes

International Nuclear Information System (INIS)

Uyar, Tamer; Besenbacher, Flemming; Nur, Yusuf; Hacaloglu, Jale

2009-01-01

Electrospinning of nanofibers with cyclodextrin inclusion complexes (CD-ICs) is particularly attractive since distinct properties can be obtained by combining the nanofibers with specific functions of the CD-ICs. Here we report on the electrospinning of poly(methyl methacrylate) (PMMA) nanofibers containing cyclodextrin-menthol inclusion complexes (CD-menthol-ICs). These CD-menthol-IC functionalized nanofibers were developed with the purpose of producing functional nanofibers that contain fragrances/flavors with high temperature stability, and menthol was used as a model fragrance/flavor material. The PMMA nanofibers were electrospun with CD-menthol-ICs using three type of CD: α-CD, β-CD, and γ-CD. Direct pyrolysis mass spectrometry (DP-MS) studies showed that the thermal evaporation of menthol occurred over a very high and a broad temperature range (100-355 deg. C) for PMMA/CDmenthol-IC nanowebs, demonstrating the complexation of menthol with the CD cavity and its high temperature stability. Furthermore, as the size of CD cavity increased in the order α-CD β-CD>α-CD.

Fabrication and properties of shape-memory polymer coated with conductive nanofiber paper

Science.gov (United States)

Lu, Haibao; Liu, Yanju; Gou, Jan; Leng, Jinsong

2009-07-01

A unique concept of shape-memory polymer (SMP) nanocomposites making up of carbon nanofiber paper was explored. The essential element of this method was to design and fabricate nanopaper with well-controlled and optimized network structure of carbon nanofibers. In this study, carbon nanofiber paper was prepared under ultrasonicated processing and vapor press method, while the dispersion of nanofiber was treated by BYK-191 dispersant. The morphologies of carbon nanofibers within the paper were characterized with scanning electron microscopy (SEM). In addition, the thermomechanical properties of SMP coated with carbon nanofiber paper were measured by the dynamic mechanical thermal analysis (DMTA). It was found that the glass transition temperature and thermomechanical properties of nanocomposites were strongly determined by the dispersion of polymer in conductive paper. Subsequently, the electrical conductivity of conductive paper and nanocomposites were measured, respectively. And experimental results revealed that the conductive properties of nanocoposites were significantly improved by carbon nanopaper, resulting in actuation driven by electrical resistive heating.

Functionalized carbon nanotubes and nanofibers for biosensing applications

Energy Technology Data Exchange (ETDEWEB)

Wang, Jun; Lin, Yuehe

2008-07-30

This review summarizes the recent advances of carbon nanotube (CNT) and carbon nanofiber (CNF)-based electrochemical biosensors with an emphasis on the applications of CNTs. Carbon nanotubes and carbon nanofibers have unique electric, electrocatalytic, and mechanical properties which make them efficient materials for the use in electrochemical biosensor development. In this article, the functionalization of CNTs for biosensors is simply discussed. The electrochemical biosensors based on CNT and their various applications, e.g., measurement of small biological molecules and environmental pollutants, detection of DNA, and immunosensing of disease biomarkers, are reviewed. Moreover, the development of carbon nanofiber-based electrochemical biosensors and their applications are outlined. Finally, some challenges are discussed in the conclusion.

Carbon-coated Li3 N nanofibers for advanced hydrogen storage.

Science.gov (United States)

Xia, Guanglin; Li, Dan; Chen, Xiaowei; Tan, Yingbin; Tang, Ziwei; Guo, Zaiping; Liu, Huakun; Liu, Zongwen; Yu, Xuebin

2013-11-20

3D porous carbon-coated Li3 N nanofibers are successfully fabricated via the electrospinning technique. The as-prepared nanofibers exhibit a highly improved hydrogen-sorption performance in terms of both thermodynamics and kinetics. More interestingly, a stable regeneration can be achieved due to the unique structure of the nanofibers, over 10 cycles of H2 sorption at a temperature as low as 250 °C. © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Synthesis and electrochemical performance of ruthenium oxide-coated carbon nanofibers as anode materials for lithium secondary batteries

Energy Technology Data Exchange (ETDEWEB)

Hyun, Yura; Choi, Jin-Yeong [Department of Chemistry, Keimyung University (Korea, Republic of); Park, Heai-Ku [Department of Chemical Engineering, Keimyung University (Korea, Republic of); Lee, Chang-Seop, E-mail: surfkm@kmu.ac.kr [Department of Chemistry, Keimyung University (Korea, Republic of)

2016-12-01

Highlights: • Ruthenium oxide (RuO{sub 2}) coated carbon nanofibers (CNFs) on Ni foam were synthesized by chemical vapor deposition method and applied as anode materials of Li secondary batteries. • When RuO{sub 2}/CNFs/Ni foam was used as the anode material, initial capacity was improved from 276 mAh/g to 494 mAh/g with retention rate of 47.4% after 30 cycles. - Abstract: In this study, ruthenium oxide (RuO{sub 2}) coated carbon nanofibers (CNFs) were synthesized and applied as anode materials of Li secondary batteries. The CNFs were grown on Ni foam via chemical vapor deposition (CVD) method after CNFs/Ni foam was put into the 0.01 M RuCl{sub 3} solution. The ruthenium oxide-coated CNFs/Ni foam was dried in a dryer at 80 °C. The morphologies, compositions, and crystal quality of RuO{sub 2}/CNFs/Ni foam were characterized by SEM, EDS, XRD, Raman spectroscopy, and XPS. The electrochemical characteristics of RuO{sub 2}/CNFs/Ni foam as anode of Li secondary batteries were investigated using three-electrode cell. The RuO{sub 2}/CNFs/Ni foam was directly employed as a working electrode without any binder, and lithium foil was used as the counter and reference electrodes. LiClO{sub 4} (1 M) was employed as electrolyte and dissolved in a mixture of propylene carbonate (PC): ethylene carbonate (EC) in a 1:1 volume ratio. The galvanostatic charge/discharge cycling and cyclic voltammetry measurements were carried out at room temperature by using a battery tester. In particular, synthesized RuO{sub 2}/CNFs/Ni foam showed the highest retention rate (47.4%). The initial capacity (494 mAh/g) was reduced to 234 mAh/g after 30 cycles.

Synthesis and electrochemical performance of ruthenium oxide-coated carbon nanofibers as anode materials for lithium secondary batteries

International Nuclear Information System (INIS)

Hyun, Yura; Choi, Jin-Yeong; Park, Heai-Ku; Lee, Chang-Seop

2016-01-01

Highlights: • Ruthenium oxide (RuO_2) coated carbon nanofibers (CNFs) on Ni foam were synthesized by chemical vapor deposition method and applied as anode materials of Li secondary batteries. • When RuO_2/CNFs/Ni foam was used as the anode material, initial capacity was improved from 276 mAh/g to 494 mAh/g with retention rate of 47.4% after 30 cycles. - Abstract: In this study, ruthenium oxide (RuO_2) coated carbon nanofibers (CNFs) were synthesized and applied as anode materials of Li secondary batteries. The CNFs were grown on Ni foam via chemical vapor deposition (CVD) method after CNFs/Ni foam was put into the 0.01 M RuCl_3 solution. The ruthenium oxide-coated CNFs/Ni foam was dried in a dryer at 80 °C. The morphologies, compositions, and crystal quality of RuO_2/CNFs/Ni foam were characterized by SEM, EDS, XRD, Raman spectroscopy, and XPS. The electrochemical characteristics of RuO_2/CNFs/Ni foam as anode of Li secondary batteries were investigated using three-electrode cell. The RuO_2/CNFs/Ni foam was directly employed as a working electrode without any binder, and lithium foil was used as the counter and reference electrodes. LiClO_4 (1 M) was employed as electrolyte and dissolved in a mixture of propylene carbonate (PC): ethylene carbonate (EC) in a 1:1 volume ratio. The galvanostatic charge/discharge cycling and cyclic voltammetry measurements were carried out at room temperature by using a battery tester. In particular, synthesized RuO_2/CNFs/Ni foam showed the highest retention rate (47.4%). The initial capacity (494 mAh/g) was reduced to 234 mAh/g after 30 cycles.

Mechanical and structural characterizations of gamma- and alpha-alumina nanofibers

Energy Technology Data Exchange (ETDEWEB)

Vahtrus, Mikk; Umalas, Madis [Institute of Physics, University of Tartu, Ravila 14c, 50412 Tartu (Estonia); Polyakov, Boris [Institute of Solid State Physics, University of Latvia, Kengaraga 8, LV-1063 Riga (Latvia); Dorogin, Leonid [Institute of Physics, University of Tartu, Ravila 14c, 50412 Tartu (Estonia); ITMO University, Kronverkskiy pr., 49, 197101 Saint Petersburg (Russian Federation); Saar, Rando; Tamme, Maret; Saal, Kristjan [Institute of Physics, University of Tartu, Ravila 14c, 50412 Tartu (Estonia); Lõhmus, Rünno [Institute of Physics, University of Tartu, Ravila 14c, 50412 Tartu (Estonia); Materials Technologies Competence Centre, Riia 185b, 51014 Tartu (Estonia); Vlassov, Sergei [Institute of Physics, University of Tartu, Ravila 14c, 50412 Tartu (Estonia)

2015-09-15

We investigate the applicability of alumina nanofibers as a potential reinforcement material in ceramic matrix compounds by comparing the mechanical properties of individual nanofibers before and after annealing at 1400 °C. Mechanical testing is performed inside a scanning electron microscope (SEM), which enables observation in real time of the deformation and fracture of the fibers under loading, thereby providing a close-up inspection of the freshly fractured area in vacuum. Improvement of both the Young's modulus and the breaking strength for annealed nanofibers is demonstrated. Mechanical testing is supplemented with the structural characterization of the fibers before and after annealing using SEM, transmission electron microscopy and X-ray diffraction methods. - Highlights: • Mechanical properties of individual alumina nanofibers were measured using in situ SEM cantilevered beam bending technique. • Improvement of mechanical properties of the alumina fibers after annealing at 1400 °C is demonstrated. • Formation of branched structures is demonstrated and their mechanical properties are studied. • XRD and electron microscopy were used for structural characterization of untreated and annealed nanofibers.

Synthesis and corrosion protection properties of poly(o-phenylenediamine nanofibers

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P. Muthirulan

2013-07-01

Full Text Available The present study shows a novel method for the synthesis of uniformly-shaped poly(othophenylediamine (PoPD nanofibers by chemical oxidative polymerization method for application towards smart corrosion resistance coatings. Transmission Electron Microscopy (TEM and Scanning Electron Microscopy (SEM studies confirm morphology of PoPD with three dimensional (3D networked dendritic superstructures having average diameter of 50–70 nm and several hundred meters of length. UV–vis and FTIR spectral results shows the formation of PoPD nanofibers containing phenazine ring ladder-structure with benzenoid and quinoid imine units. Thermogravimetric analyses (TGA of PoPD nanofibers possess good thermal stability. The anti-corrosion behavior of PoPD nanofibers on 316L SS was investigated in 3.5% NaCl solution using potentiodynamic polarization and electrochemical impedance spectroscopic (EIS measurements. The PoPD coated 316L SS exhibits higher corrosion potential when compared to uncoated specimen. EIS studies, clearly ascertain that PoPD nanofiber coatings exhibits excellent potential barrier to protect the 316L SS against corrosion in 3.5% NaCl.

Enhancement of Ultrahigh Performance Concrete Material Properties with Carbon Nanofiber

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Libya Ahmed Sbia

2014-01-01

Full Text Available Ultrahigh performance concrete (UHPC realized distinctly high mechanical, impermeability, and durability characteristics by reducing the size and content of capillary pore, refining the microstructure of cement hydrates, and effectively using fiber reinforcement. The dense and fine microstructure of UHPC favor its potential to effectively disperse and interact with nanomaterials, which could complement the reinforcing action of fibers in UHPC. An optimization experimental program was implemented in order to identify the optimum combination of steel fiber and relatively low-cost carbon nanofiber in UHPC. The optimum volume fractions of steel fiber and carbon nanofiber identified for balanced improvement of flexural strength, ductility, energy sorption capacity, impact, and abrasion resistance of UHPC were 1.1% and 0.04%, respectively. Desired complementary/synergistic actions of nanofibers and steel fibers in UHPC were detected, which were attributed to their reinforcing effects at different scales, and the potential benefits of nanofibers to interfacial bonding and pull-out behavior of fibers in UHPC. Modification techniques which enhanced the hydrophilicity and bonding potential of nanofibers to cement hydrates benefited their reinforcement efficiency in UHPC.

Incorporation of functionalized gold nanoparticles into nanofibers for enhanced attachment and differentiation of mammalian cells

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Jung Dongju

2012-06-01

Full Text Available Abstract Background Electrospun nanofibers have been widely used as substrata for mammalian cell culture owing to their structural similarity to natural extracellular matrices. Structurally consistent electrospun nanofibers can be produced with synthetic polymers but require chemical modification to graft cell-adhesive molecules to make the nanofibers functional. Development of a facile method of grafting functional molecules on the nanofibers will contribute to the production of diverse cell type-specific nanofiber substrata. Results Small molecules, peptides, and functionalized gold nanoparticles were successfully incorporated with polymethylglutarimide (PMGI nanofibers through electrospinning. The PMGI nanofibers functionalized by the grafted AuNPs, which were labeled with cell-adhesive peptides, enhanced HeLa cell attachment and potentiated cardiomyocyte differentiation of human pluripotent stem cells. Conclusions PMGI nanofibers can be functionalized simply by co-electrospinning with the grafting materials. In addition, grafting functionalized AuNPs enable high-density localization of the cell-adhesive peptides on the nanofiber. The results of the present study suggest that more cell type-specific synthetic substrata can be fabricated with molecule-doped nanofibers, in which diverse functional molecules are grafted alone or in combination with other molecules at different concentrations.

Influence of polyvinyl alcohol amount on producing in situ photo-crosslinked thioamide functionalized nanofiber membranes

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Zeytuncu Bihter

2015-01-01

Full Text Available Poly(vinyl alcohol/maleic anhydride/acryloyl thioamide monomer (PVA/MA/ATM photo-cured nanofiber membranes and pure PVA nanofiber membranes were produced by electrospinning technique. In situ UV radiation was applied during the electrospinning in order to provide polymerization during the jet flight and promote crosslinking of ATM and MA with PVA. The cross-linking was examined by Fourier-transform infrared spectroscopy (FTIR. The morphology and thermal behavior of electrospun nanofiber were characterized by scanning electron microscope (SEM and thermogravimetric analysis (TGA, respectively. The surface area of nanofiber membranes was measured by Brunauer-Emmert-Teller (BET analysis. Furthermore, water durability test was examined. Water durability test demonstrated that in situ photo-cured PVA/MA/ATM nanofiber membrane had the least average mass loss. The surface areas of PVA/MA/ATM nanofiber membranes were 160-280 m2/g. The surface area and diameter of PVA/MA/ATM nanofibers decreased as the PVA content increased. The diameter of nanofibers was obtained less than 100 nm. The results showed that the water-insoluble nanofiber membranes with better chemical and thermal resistance were obtained. These nanofiber membranes may be a promising candidate for the usage of water treatment.

Experimental Investigation of the Properties of Electrospun Nanofibers for Potential Medical Application

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Anhui Wang

2015-01-01

Full Text Available Polymer based nanofibers using ethylene-co-vinyl alcohol (EVOH were fabricated by electrospinning technology. The nanofibers were studied for potential use as dressing materials for skin wounds treatment. Properties closely related to the clinical requirements for wound dressing were investigated, including the fluid uptake ability (FUA, the water vapour transmission rate (WVTR, the bacteria control ability of nanofibers encapsulated with different antibacterial drugs, and Ag of various concentrations. Nanofibre degradation under different environmental conditions was also studied for the prospect of long term usage. The finding confirms the potential of EVOH nanofibers for wound dressing application, including the superior performance compared to cotton gauze and the strong germ killing capacity when Ag particles are present in the nanofibers.

A super hydrophilic modification of poly(vinylidene fluoride) (PVDF) nanofibers: By in situ hydrothermal approach

Science.gov (United States)

Sheikh, Faheem A.; Zargar, Mohammad Afzal; Tamboli, Ashif H.; Kim, Hern

2016-11-01

Nanofibers fabricated from Poly(vinylidene fluoride) (PVDF) possesses potential applications in the field of filtrations, because of their excellent resistance towards harsh chemicals. However, the hydrophobicity restricts its further application. In this work, we focus on optimal parameters for post-electrospun tethering of Poly(vinyl alcohol) (PVA) as superhydrophilic domain onto each individual PVDF nanofibers by exploiting the in situ hydrothermal approach. The results indicated an increase in nanofiber diameters due to coating of PVA and improved surface wettability of PVDF nanofibers. The tensile tests of nanofibers indicated that mechanical properties of PVDF nanofibers could be sharply tuned from rigid to ductile. Furthermore, the studies strongly suggest that in situ hydrothermal treatment of post-electrospun nanofibers can improve the water contact angle and these nanofibers can be used in varied applications (e.g., in water purification systems).

Hollow NiO nanofibers modified by citric acid and the performances as supercapacitor electrode

International Nuclear Information System (INIS)

Ren, Bo; Fan, Meiqing; Liu, Qi; Wang, Jun; Song, Dalei; Bai, Xuefeng

2013-01-01

Graphical abstract: The possible formation process of NiO nanofibers without citric acid (a), and modified by citric acid (b). When the nanofibers is modified by citric acid, the nickel citrate is produced by complexing action of citric acid and nickel nitrate. Because of the larger space steric hindrance, the structure is limited by the molecular geometry. Under high temperature, the hollow nanofibers composed of NiO slices formed after the removal of PVP. Highlights: ► The method of obtaining hollow nanofibers is raised for the first time. ► The prepared NiO nanofibers are hollow tube and comprised of many NiO sheets. ► The hollow structure facilitated the electrolyte penetration. ► The hollow NiO nanofibers have good electrochemical properties. -- Abstract: NiO nanofibers modified by citric acid (NiO/CA) for supercapacitor material have been fabricated by electrospinning process. The characterizations of the nanofibers are investigated by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Electrochemical properties are characterized by cyclic voltammetry, galvanostatic charge/discharge measurements, and electrochemical impedance spectroscopy. Results show that the NiO/CA nanofibers are hollow tube and comprised of many NiO sheets. Furthermore, the NiO/CA nanofibers have good electrochemical reversibility and display superior capacitive performance with large capacitance (336 F g −1 ), which is 2.5 times of NiO electrodes. Moreover, the NiO/CA nanofibers show excellent cyclic performance after 1000 cycles

Copper-Containing Anti-Biofilm Nanofiber Scaffolds as a Wound Dressing Material.

Directory of Open Access Journals (Sweden)

Jayesh J Ahire

Full Text Available Copper particles were incorporated into nanofibers during the electrospinning of poly-D,L-lactide (PDLLA and poly(ethylene oxide (PEO. The ability of the nanofibers to prevent Pseudomonas aeruginosa PA01 and Staphylococcus aureus (strain Xen 30 to form biofilms was tested. Nanofibers containing copper particles (Cu-F were thinner (326 ± 149 nm in diameter, compared to nanofibers without copper (CF; 445 ± 93 nm in diameter. The crystalline structure of the copper particles in Cu-F was confirmed by X-ray diffraction (XRD. Copper crystals were encapsulated, but also attached to the surface of Cu-F, as shown scanning transmission electron microscopy (STEM and transmission electron microscopy (TEM, respectively. The copper particles had no effect on the thermal degradation and thermal behaviour of Cu-F, as shown by thermogravimetric analysis (TGA and differential scanning calorimeter (DSC. After 48 h in the presence of Cu-F, biofilm formation by P. aeruginosa PA01 and S. aureus Xen 30 was reduced by 41% and 50%, respectively. Reduction in biofilm formation was ascribed to copper released from the nanofibers. Copper-containing nanofibers may be incorporated into wound dressings.

Isolation of aramid nanofibers for high strength multiscale fiber reinforced composites

Science.gov (United States)

Lin, Jiajun; Patterson, Brendan A.; Malakooti, Mohammad H.; Sodano, Henry A.

2018-03-01

Aramid fibers are famous for their high specific strength and energy absorption properties and have been intensively used for soft body armor and ballistic protection. However, the use of aramid fiber reinforced composites is barely observed in structural applications. Aramid fibers have smooth and inert surfaces that are unable to form robust adhesion to polymeric matrices due to their high crystallinity. Here, a novel method to effectively integrate aramid fibers into composites is developed through utilization of aramid nanofibers. Aramid nanofibers are prepared from macroscale aramid fibers (such as Kevlar®) and isolated through a simple and scalable dissolution method. Prepared aramid nanofibers are dispersible in many polymers due to their improved surface reactivity, meanwhile preserve the conjugated structure and likely the strength of their macroscale counterparts. Simultaneously improved elastic modulus, strength and fracture toughness are observed in aramid nanofiber reinforced epoxy nanocomposites. When integrated in continuous fiber reinforced composites, aramid nanofibers can also enhance interfacial properties by forming hydrogen bonds and π-π coordination to bridge matrix and macroscale fibers. Such multiscale reinforcement by aramid nanofibers and continuous fibers results in strong polymeric composites with robust mechanical properties that are necessary and long desired for structural applications.

Hydrothermal synthesis, characterization, and luminescence of Ca{sub 2}B{sub 2}O{sub 5}:RE (RE = Eu{sup 3+}, Tb{sup 3+}, Dy{sup 3+}) nanofibers

Energy Technology Data Exchange (ETDEWEB)

Yang, Li; Wan, Yingpeng; Li, Yuze; Pu, Yinfu; Huang, Yanlin, E-mail: huang@suda.edu.cn [Soochow University, State and Local Joint Engineering Laboratory for Novel Functional Polymeric Materials, College of Chemistry, Chemical Engineering and Materials Science (China); Chen, Cuili; Seo, Hyo Jin, E-mail: hjseo@pknu.ac.kr [Pukyong National University, Department of Physics and Interdisciplinary Program of Biomedical Engineering (Korea, Republic of)

2016-04-15

Ca{sub 2}B{sub 2}O{sub 5}:RE (RE = Eu{sup 3+}, Tb{sup 3+}, Dy{sup 3+}) nanofibers were synthesized by the hydrothermal reaction method. The structural refinement was conducted on the base of the X-ray powder diffraction (XRD) measurements. The surface properties of the Ca{sub 2}B{sub 2}O{sub 5}:RE (RE = Eu{sup 3+}, Tb{sup 3+}, Dy{sup 3+}) nanofibers were investigated by the measurements such as the scanning electron microscope (SEM), transmission electron microscope (TEM), and the energy dispersive spectrum (EDS). The nanofiber has a diameter of about 100 nm and a length of several micrometers. The luminescence properties such as photoluminescence excitation (PLE) and emission spectra (PL), decay lifetime, color coordinates, and the absolute internal quantum efficiency (QE) were reported. Ca{sub 2}B{sub 2}O{sub 5}:Eu{sup 3+} nanofibers show the red luminescence with CIE coordinates of (x = 0.41, y = 0.51) and the luminescence lifetime of 0.63 ms. The luminescence of Ca{sub 2}B{sub 2}O{sub 5}:Tb{sup 3+} nanofibers is green color (x = 0.29, y = 0.53) with the lifetime of 2.13 ms. However, Dy{sup 3+}-doped Ca{sub 2}B{sub 2}O{sub 5} nanofibers present a single-phase white-color phosphor with the fluorescence decay of 3.05 ms. Upon near-UV excitation, the absolute quantum efficiency is measured to be 65, 35, and 37 % for Eu{sup 3+}-, Tb{sup 3+}-, Dy{sup 3+}-doped Ca{sub 2}B{sub 2}O{sub 5} nanofibers, respectively. It is suggested that Ca{sub 2}B{sub 2}O{sub 5}:RE (RE = Eu{sup 3+}, Tb{sup 3+}, Dy{sup 3+}) nanofibers could be an efficient phosphor for lighting and display.

Preparation and application of magnetic superhydrophobic polydivinylbenzene nanofibers for oil adsorption in wastewater.

Science.gov (United States)

Zhu, Xiaobiao; Tian, Ye; Li, Feifei; Liu, Yapeng; Wang, Xiaohui; Hu, Xiang

2018-06-01

Superhydrophobic materials have an excellent performance in oil adsorption. In this study, a novel magnetic polydivinylbenzene (PDVB) nanofiber was synthesized by the method of cation polymerization to adsorb oil from water. The magnetic PDVB was hollow nanofiber with Fe 3 O 4 nanoparticles embedded in its structure. The synthesis condition was optimized that the ratio of divinylbenzene (DVB) to boron fluoride ethyl ether (BFEE) was 10:1 (v/v), and the Fe 3 O 4 dosage was 0.175 g/g of DVB. The material showed an excellent oil adsorption performance in wastewater, and the oil concentration could be reduced from 2000 to 92.2 mg/L within 5 min. The magnetic PDVB had relatively high adsorption capacity (12 g/g) for oil, which could be attributed to its super hydrophobicity and one-dimensional nanostructure with high crosslinking degree. The isotherm study indicated that the magnetic PDVB adsorbed oil was an asymmetric or multilayer adsorption process. The material could be regenerated by simple squeeze and maintain its adsorption capacity after it has been used for 10 recycles. In real coking wastewater, the magnetic PDVB kept a good oil adsorption performance without the interference of various pollutants, indicating a wide prospect in practical use.

Physicochemical investigations of carbon nanofiber supported Cu/ZrO2 catalyst

International Nuclear Information System (INIS)

Din, Israf Ud; Shaharun, Maizatul S.; Subbarao, Duvvuri; Naeem, A.

2014-01-01

Zirconia-promoted copper/carbon nanofiber catalysts (Cu‐ZrO 2 /CNF) were prepared by the sequential deposition precipitation method. The Herringbone type of carbon nanofiber GNF-100 (Graphite nanofiber) was used as a catalyst support. Carbon nanofiber was oxidized to (CNF-O) with 5% and 65 % concentration of nitric acid (HNO 3 ). The CNF activated with 5% HNO 3 produced higher surface area which is 155 m 2 /g. The catalyst was characterized by X-ray Diffraction (XRD), Fourier Transform Infra-Red (FTIR) and N 2 adsorption-desorption. The results showed that increase of HNO 3 concentration reduced the surface area and porosity of the catalyst

Process parameter and surface morphology of pineapple leaf electrospun nanofibers (PALF)

Science.gov (United States)

Surip, S. N.; Aziz, F. M. A.; Bonnia, N. N.; Sekak, K. A.; Zakaria, M. N.

2017-09-01

In recent times, nanofibers have attracted the attention of researchers due to their pronounced micro and nano structural characteristics that enable the development of advanced materials that have sophisticated applications. The production of nanofibers by the electrospinning process is influenced both by the electrostatic forces and the viscoelastic behavior of the polymer. Process parameters, like solution feed rate, applied voltage, nozzle-collector distance, and spinning environment, and material properties, like solution concentration, viscosity, surface tension, conductivity, and solvent vapor pressure, influence the structure and properties of electrospun nanofibers. Significant work has been done to characterize the properties of PALF nanofibers as a function of process and material parameters.

Simultaneous synthesis of polyaniline nanofibers and metal (Ag and Pt) nanoparticles

International Nuclear Information System (INIS)

Huang, Li-Ming; Liao, Wei-Hao; Ling, Han-Chern; Wen, Ten-Chin

2009-01-01

An approach for the synthesis of Ag/Pt nanoparticle-incorporated polyaniline (PANI) nanofibers and Ag/Pt nanoparticles was developed that considers both thermodynamic and kinetic aspects. Ag/Pt nanoparticles and PANI nanofibers are generated simultaneously by the reduction of Ag + /Pt 4+ ions to Ag/Pt nanoparticles and by the polymerization of aniline (ANI) to PANI nanofibers. The PANI nanofibers serve as anchor seeds for the formation of Ag/Pt nanoparticles. The simple and inexpensive route for the preparation of PANI-Ag/Pt nanocomposites can be extended to the polymerization of ANI derivatives and the formation of metal/metal oxides for applications such as sensors, direct methanol fuel cells, and capacitors.

Modeling Temperature Dependent Singlet Exciton Dynamics in Multilayered Organic Nanofibers

DEFF Research Database (Denmark)

de Sousa, Leonardo Evaristo; de Oliveira Neto, Pedro Henrique; Kjelstrup-Hansen, Jakob

2018-01-01

Organic nanofibers have shown potential for application in optoelectronic devices because of the tunability of their optical properties. These properties are influenced by the electronic structure of the molecules that compose the nanofibers, but also by the behavior of the excitons generated...... dynamics in multilayered organic nanofibers. By simulating absorption and emission spectra, the possible Förster transitions are identified. Then, a Kinetic Monte Carlo (KMC) model is employed in combination with a genetic algorithm to theoretically reproduce time resolved photoluminescence measurements...

Preparation and characterization of Ce-doped ZnO nanofibers by an electrospinning method

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Jong-Pil Kim

2011-02-01

Full Text Available ZnO and Ce-doped ZnO Nanofibers on (111 Pt/SiO2/Si substrates were produced using an electrospinning technique. The as-prepared composite fibres were subjected to high-temperature calcination to produce inorganic fibers. After calcining at a temperature of 500 °C, the average diameter of the ZnO and Ce-doped ZnO nanofibers were determined to be 170 nm and 225 nm, respectively. The average grain size of the ZnO and Ce-doped ZnO nanofibers were about 50 nm and 57 nm, respectively. The microstructure, chemical bonding state and photoluminescence of the produced ZnO and Ce-doped ZnO nanofibers were investigated. The Ce-doped ZnO nanofiber can be assigned to the presence of Ce ions on substitutional sites of Zn ions and the Ce3+ state from X-ray photoelectron spectra. Compared with PL spectra of ZnO nanofibers, the peak position of the UV emission of the Ce-doped ZnO nanofibers is sharply suppressed while the green emission band is highly enhanced.

Development of bimetal-grown multi-scale carbon micro-nanofibers as an immobilizing matrix for enzymes in biosensor applications

Energy Technology Data Exchange (ETDEWEB)

Hood, Amit R. [Department of Chemical Engineering, Indian Institute of Technology, Kanpur (India); Saurakhiya, Neelam; Deva, Dinesh [DST Unit on Nanosciences, Kanpur, 208016 (India); Sharma, Ashutosh [Department of Chemical Engineering, Indian Institute of Technology, Kanpur (India); DST Unit on Nanosciences, Kanpur, 208016 (India); Verma, Nishith, E-mail: nishith@iitk.ac.in [Department of Chemical Engineering, Indian Institute of Technology, Kanpur (India); Center for Environmental Science and Engineering, Kanpur 208016 (India)

2013-10-15

This study describes the development of a novel bimetal (Fe and Cu)-grown hierarchical web of carbon micro-nanofiber-based electrode for biosensor applications, in particular to detect glucose in liquids. Carbon nanofibers (CNFs) are grown on activated carbon microfibers (ACFs) by chemical vapor deposition (CVD) using Cu and Fe as the metal catalysts. The transition metal-fiber composite is used as the working electrode of a biosensor applied to detect glucose in liquids. In such a bi-nanometal-grown multi-scale web of ACF/CNF, Cu nanoparticles adhere to the ACF-surface, whereas Fe nanoparticles used to catalyze the growth of nanofibers attach to the CNF tips. By ultrasonication, Fe nanoparticles are dislodged from the tips of the CNFs. Glucose oxidase (GOx) is subsequently immobilized on the tips by adsorption. The dispersion of Cu nanoparticles at the substrate surface results in increased conductivity, facilitating electron transfer from the glucose solution to the ACF surface during the enzymatic reaction with glucose. The prepared Cu-ACF/CNF/GOx electrode is characterized for various surface and physicochemical properties by different analytical techniques, including scanning electron microscopy (SEM), electron dispersive X-ray analysis (EDX), Fourier-transform infrared spectroscopy (FTIR), BET surface area analysis, and transmission electron microscopy (TEM). The electrochemical tests show that the prepared electrode has fast response current, electrochemical stability, and high electron transfer rate, corroborated by CV and calibration curves. The prepared transition metal-based carbon electrode in this study is cost-effective, simple to develop, and has a stable immobilization matrix for enzymes. - Graphical abstract: A novel bimetal (Fe and Cu)-grown hierarchical web of carbon micro-nanofiber-based electrode is synthesized for biosensor applications, in particular to detect glucose in liquids. Carbon nanofibers are grown on activated carbon microfibers by

Development of bimetal-grown multi-scale carbon micro-nanofibers as an immobilizing matrix for enzymes in biosensor applications

International Nuclear Information System (INIS)

Hood, Amit R.; Saurakhiya, Neelam; Deva, Dinesh; Sharma, Ashutosh; Verma, Nishith

2013-01-01

This study describes the development of a novel bimetal (Fe and Cu)-grown hierarchical web of carbon micro-nanofiber-based electrode for biosensor applications, in particular to detect glucose in liquids. Carbon nanofibers (CNFs) are grown on activated carbon microfibers (ACFs) by chemical vapor deposition (CVD) using Cu and Fe as the metal catalysts. The transition metal-fiber composite is used as the working electrode of a biosensor applied to detect glucose in liquids. In such a bi-nanometal-grown multi-scale web of ACF/CNF, Cu nanoparticles adhere to the ACF-surface, whereas Fe nanoparticles used to catalyze the growth of nanofibers attach to the CNF tips. By ultrasonication, Fe nanoparticles are dislodged from the tips of the CNFs. Glucose oxidase (GOx) is subsequently immobilized on the tips by adsorption. The dispersion of Cu nanoparticles at the substrate surface results in increased conductivity, facilitating electron transfer from the glucose solution to the ACF surface during the enzymatic reaction with glucose. The prepared Cu-ACF/CNF/GOx electrode is characterized for various surface and physicochemical properties by different analytical techniques, including scanning electron microscopy (SEM), electron dispersive X-ray analysis (EDX), Fourier-transform infrared spectroscopy (FTIR), BET surface area analysis, and transmission electron microscopy (TEM). The electrochemical tests show that the prepared electrode has fast response current, electrochemical stability, and high electron transfer rate, corroborated by CV and calibration curves. The prepared transition metal-based carbon electrode in this study is cost-effective, simple to develop, and has a stable immobilization matrix for enzymes. - Graphical abstract: A novel bimetal (Fe and Cu)-grown hierarchical web of carbon micro-nanofiber-based electrode is synthesized for biosensor applications, in particular to detect glucose in liquids. Carbon nanofibers are grown on activated carbon microfibers by

Interpenetrated Binary Supramolecular Nanofibers for Sensitive Fluorescence Detection of Six Classes of Explosives.

Science.gov (United States)

Xiong, Wei; Zhu, Qijian; Gong, Yanjun; Wang, Chen; Che, Yanke; Zhao, Jincai

2018-04-03

In this work, we develop a sequential self-assembly approach to fabricate interpenetrated binary supramolecular nanofibers consisting of carbazole oligomer 1-cobalt(II) (1-Co 2+ ) coordination nanofibers and oligomer 2 nanofibers for the sensitive detection of six classes of explosives. When exposed to peroxide explosives (e.g., H 2 O 2 ), Co 2+ in 1-Co 2+ coordination nanofibers can be reduced to Co + that can transfer an electron to the excited 2 nanofibers and thereby quench their fluorescence. On the other hand, when exposed to the other five classes of explosives, the excited 2 nanofibers can transfer an electron to explosives to quench their fluorescence. On the basis of the distinct fluorescence quenching mechanisms, six classes of explosives can be sensitively detected. Herein, we provide a new strategy to design broad-band fluorescence sensors for a rich identification of threats.

Evaluation of carbon fiber composites modified by in situ incorporation of carbon nanofibers

Directory of Open Access Journals (Sweden)

André Navarro de Miranda

2011-12-01

Full Text Available Nano-carbon materials, such as carbon nanotubes and carbon nanofibers, are being thought to be used as multifunctional reinforcement in composites. The growing of carbon nanofiber at the carbon fiber/epoxy interface results in composites having better electrical properties than conventional carbon fiber/epoxy composites. In this work, carbon nanofibers were grown in situ over the surface of a carbon fiber fabric by chemical vapor deposition. Specimens of carbon fiber/nanofiber/epoxy (CF/CNF/epoxy composites were molded and electrical conductivity was measured. Also, the CF/CNF/epoxy composites were tested under flexure and interlaminar shear. The results showed an overall reduction in mechanical properties as a function of added nanofiber, although electrical conductivity increased up to 74% with the addition of nanofibers. Thus CF/CNF/epoxy composites can be used as electrical dissipation discharge materials.

Precisely Assembled Nanofiber Arrays as a Platform to Engineer Aligned Cell Sheets for Biofabrication

Directory of Open Access Journals (Sweden)

Vince Beachley

2014-08-01

Full Text Available A hybrid cell sheet engineering approach was developed using ultra-thin nanofiber arrays to host the formation of composite nanofiber/cell sheets. It was found that confluent aligned cell sheets could grow on uniaxially-aligned and crisscrossed nanofiber arrays with extremely low fiber densities. The porosity of the nanofiber sheets was sufficient to allow aligned linear myotube formation from differentiated myoblasts on both sides of the nanofiber sheets, in spite of single-side cell seeding. The nanofiber content of the composite cell sheets is minimized to reduce the hindrance to cell migration, cell-cell contacts, mass transport, as well as the foreign body response or inflammatory response associated with the biomaterial. Even at extremely low densities, the nanofiber component significantly enhanced the stability and mechanical properties of the composite cell sheets. In addition, the aligned nanofiber arrays imparted excellent handling properties to the composite cell sheets, which allowed easy processing into more complex, thick 3D structures of higher hierarchy. Aligned nanofiber array-based composite cell sheet engineering combines several advantages of material-free cell sheet engineering and polymer scaffold-based cell sheet engineering; and it represents a new direction in aligned cell sheet engineering for a multitude of tissue engineering applications.

(Au/PANA/PVAc) nanofibers as a novel composite matrix for albumin and streptavidin immobilization

Energy Technology Data Exchange (ETDEWEB)

Golshaei, Rana [University of Kashan, Institute of Nano Science and Nano Technology, Kashan, P.O. Box 87317-51167, Islamic Republic of Iran (Iran, Islamic Republic of); Guler, Zeliha [Istanbul Technical University, Nanoscience and Nanoengineering, Maslak, Istanbul 34469 (Turkey); Sarac, Sezai A., E-mail: sarac@itu.edu.tr [Istanbul Technical University, Nanoscience and Nanoengineering, Maslak, Istanbul 34469 (Turkey); Istanbul Technical University, Department of Chemistry and Polymer Science and Technology, Maslak, Istanbul 34469 (Turkey)

2016-03-01

A novel electrospun nanofiber mat (Au/PANA/PVAc) consists of (Gold/Poly Anthranilic acid) (Au/PANA) core/shell nanostructures as a support material for protein immobilization that was developed and characterized by electrochemical impedance spectroscopy. In the core/shells, PANA served carboxyl groups (− COOH) for covalent protein immobilization and Au enhanced the electrochemical properties by acting as tiny conduction centers to facilitate electron transfer. Covalent immobilization of albumin and streptavidin as model proteins onto the (Au/PANA/PVAc) nanofibers was carried out by using 1-ethyl-3-(dimethyl-aminopropyl) carbodiimide hydrochloride (EDC)/N-hydroxyl succinimide (NHS) activation. PVAc nanofibers were compared with Au/PANA/PVAc nanofibers before and after protein immobilization. The successful covalent binding of both albumin and streptavidin onto (Au/PANA/PVAc) nanofibers was confirmed by FTIR-ATR, Electron Microscopy/Energy-Dispersive X-ray Spectroscopy SEM/EDX and Electrochemical impedance spectroscopy (EIS). The nanofibers became resistive due to protein immobilization and the higher charge transfer resistance was observed after higher amount of protein was immobilized. - Highlights: • Au/PANA/PVAc nanofibers with (COOH) groups as a suitable supports for covalent immobilization of proteins. • Increasing of the resistivity of the nanofibers after immobilization of the proteins. • Activation of Au/PANA/PVAc nanofibers by using EDC/NHS.

Bacterial-cellulose-derived interconnected meso-microporous carbon nanofiber networks as binder-free electrodes for high-performance supercapacitors

Science.gov (United States)

Hao, Xiaodong; Wang, Jie; Ding, Bing; Wang, Ya; Chang, Zhi; Dou, Hui; Zhang, Xiaogang

2017-06-01

Bacterial cellulose (BC), a typical biomass prepared from the microbial fermentation process, has been proved that it can be an ideal platform for design of three-dimensional (3D) multifunctional nanomaterials in energy storage and conversion field. Here we developed a simple and general silica-assisted strategy for fabrication of interconnected 3D meso-microporous carbon nanofiber networks by confine nanospace pyrolysis of sustainable BC, which can be used as binder-free electrodes for high-performance supercapacitors. The synthesized carbon nanofibers exhibited the features of interconnected 3D networks architecture, large surface area (624 m2 g-1), mesopores-dominated hierarchical porosity, and high graphitization degree. The as-prepared electrode (CN-BC) displayed a maximum specific capacitance of 302 F g-1 at a current density of 0.5 A g-1, high-rate capability and good cyclicity in 6 M KOH electrolyte. This work, together with cost-effective preparation strategy to make high-value utilization of cheap biomass, should have significant implications in the green and mass-producible energy storage.

Electrospun Blank Nanocoating for Improved Sustained Release Profiles from Medicated Gliadin Nanofibers

Directory of Open Access Journals (Sweden)

Xinkuan Liu

2018-03-01

Full Text Available Nanomaterials providing sustained release profiles are highly desired for efficacious drug delivery. Advanced nanotechnologies are useful tools for creating elaborate nanostructure-based nanomaterials to achieve the designed functional performances. In this research, a modified coaxial electrospinning was explored to fabricate a novel core-sheath nanostructure (nanofibers F2, in which a sheath drug-free gliadin layer was successfully coated on the core ketoprofen (KET-gliadin nanocomposite. A monolithic nanocomposite (nanofibers F1 that was generated through traditional blending electrospinning of core fluid was utilized as a control. Scanning electron microscopy demonstrated that both nanofibers F1 and F2 were linear. Transmission electron microscopy verified that nanofibers F2 featured a clear core-sheath nanostructure with a thin sheath layer about 25 nm, whereas their cores and nanofibers F1 were homogeneous KET-gliadin nanocomposites. X-ray diffraction patterns verified that, as a result of fine compatibility, KET was dispersed in gliadin in an amorphous state. In vitro dissolution tests demonstrated that the thin blank nanocoating in nanofibers F2 significantly modified drug release kinetics from a traditional exponential equation of nanofibers F1 to a zero-order controlled release model, linearly freeing 95.7 ± 4.7% of the loaded cargoes over a time period of 16 h.

Electrospun Blank Nanocoating for Improved Sustained Release Profiles from Medicated Gliadin Nanofibers.

Science.gov (United States)

Liu, Xinkuan; Shao, Wenyi; Luo, Mingyi; Bian, Jiayin; Yu, Deng-Guang

2018-03-22

Nanomaterials providing sustained release profiles are highly desired for efficacious drug delivery. Advanced nanotechnologies are useful tools for creating elaborate nanostructure-based nanomaterials to achieve the designed functional performances. In this research, a modified coaxial electrospinning was explored to fabricate a novel core-sheath nanostructure (nanofibers F2), in which a sheath drug-free gliadin layer was successfully coated on the core ketoprofen (KET)-gliadin nanocomposite. A monolithic nanocomposite (nanofibers F1) that was generated through traditional blending electrospinning of core fluid was utilized as a control. Scanning electron microscopy demonstrated that both nanofibers F1 and F2 were linear. Transmission electron microscopy verified that nanofibers F2 featured a clear core-sheath nanostructure with a thin sheath layer about 25 nm, whereas their cores and nanofibers F1 were homogeneous KET-gliadin nanocomposites. X-ray diffraction patterns verified that, as a result of fine compatibility, KET was dispersed in gliadin in an amorphous state. In vitro dissolution tests demonstrated that the thin blank nanocoating in nanofibers F2 significantly modified drug release kinetics from a traditional exponential equation of nanofibers F1 to a zero-order controlled release model, linearly freeing 95.7 ± 4.7% of the loaded cargoes over a time period of 16 h.

Zirconium Hydroxide-coated Nanofiber Mats for Nerve Agent Decontamination.

Science.gov (United States)

Kim, Sohee; Ying, Wu Bin; Jung, Hyunsook; Ryu, Sam Gon; Lee, Bumjae; Lee, Kyung Jin

2017-03-16

Diverse innovative fabrics with specific functionalities have been developed for requirements such as self-decontamination of chemical/biological pollutants and toxic nerve agents. In this work, Zr(OH) 4 -coated nylon-6,6 nanofiber mats were fabricated for the decontamination of nerve agents. Nylon-6,6 fabric was prepared via the electrospinning process, followed by coating with Zr(OH) 4 , which was obtained by the hydrolysis of Zr(OBu) 4 by a sol-gel reaction on nanofiber surfaces. The reaction conditions were optimized by varying the amounts of Zr(OBu) 4 ,the reaction time, and the temperature of the sol-gel reaction. The composite nanofibers show high decontamination efficiency against diisopropylfluorophosphate, which is a nerve agent analogue, due to its high nucleophilicity that aids in the catalysis of the hydrolysis of the phosphonate ester bonds. Composite nanofiber mats have a large potential and can be applied in specific fields such as military and medical markets. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

A review on electrospun nanofibers for oral drug delivery

Directory of Open Access Journals (Sweden)

Abbas Akhgari

2017-10-01

Full Text Available Nowadays, polymer nanofibers have gained attention due to remarkable characteristics such as high porosity and large surface area to volume ratio. Among their fabrication methods, electrospinning technique has been attracted as a simple and reproducible approach. It is a versatile, simple and cost-effective technique for the production of continuous nanofibers with acceptable characteristics such as high porosity, high surface area to volume ratio, high loading capacity and encapsulation efficiency, delivery of multiple drugs, and enhancement of drug solubility. Due to these properties electrospun nanofibers have been extensively used for different biomedical applications including wound dressing, tissue engineering, enzyme immobilization, artificial organs, and drug delivery. Different synthetic and natural polymers have been successfully electrospun into ultrafine fibers. Using electrospun nanofibers as vehicles for oral drug delivery has been investigated in different release manners- fast, biphasic or sustained release. This article presents a review on application of electrospinning technique in oral drug delivery.

A co-confined carbonization approach to aligned nitrogen-doped mesoporous carbon nanofibers and its application as an adsorbent

International Nuclear Information System (INIS)

Chen, Aibing; Liu, Chao; Yu, Yifeng; Hu, Yongqi; Lv, Haijun; Zhang, Yue; Shen, Shufeng; Zhang, Jian

2014-01-01

Highlights: • MCNFs were synthesized by a co-confined carbonization method. • The diameter size of MCNFs with bimodal mesoporous structure can be modulated. • The obtained MCNFs manifest better adsorption capacity for SO 2 , CO 2 and Cd 2+ . - Abstract: Nitrogen-doped carbon nanofibers (MCNFs) with an aligned mesoporous structure were synthesized by a co-confined carbonization method using anodic aluminum oxide (AAO) membrane and tetraethylorthosilicate (TEOS) as co-confined templates and ionic liquids as the precursor. The as-synthesized MCNFs with the diameter of 80–120 nm possessed a bulk nitrogen content of 5.3 wt% and bimodal mesoporous structure. The nitrogen atoms were mostly bound to the graphitic network in two forms, i.e. pyridinic and pyrrolic nitrogen, providing adsorption sites for acidic gases like SO 2 and CO 2 . Cyclic experiments revealed a considerable stability of MCNFs over 20 runs of SO 2 adsorption and 15 runs for CO 2 adsorption. The MCNFs also have a preferable adsorption performance for Cd 2+

Conductive Au nanowires regulated by silk fibroin nanofibers

Science.gov (United States)

Dong, Bo-Ju; Lu, Qiang

2014-03-01

Conductive Au-biopolymer composites have promising applications in tissue engineering such as nerve tissue regeneration. In this study, silk fibroin nanofibers were formed in aqueous solution by regulating silk self-assembly process and then used as template for Au nanowire fabrication. We performed the synthesis of Au seeds by repeating the seeding cycles for several times in order to increase the density of Au seeds on the nanofibers. After electroless plating, densely decorated Au seeds grew into irregularly shaped particles following silk nanofiber to fill the gaps between particles and finally form uniform continuous nanowires. The conductive property of the Au-silk fibroin nanowires was studied with current-voltage ( I-V) measurement. A typical ohmic behavior was observed, which highlighted their potential applications in nerve tissue regeneration.

Bubble-electrospinning: a novel method for making nanofibers

International Nuclear Information System (INIS)

Liu, Y; He, J-H; Yu, J-Y

2008-01-01

Nanofibers produced by electrospinning are already being used in a vast array of products in many industries. However, the volume of production of nanofibers has been being a bottleneck restricting their applications. In this work we reported a novel method to fabricate continuous and uniform nanofibers by electrospinning using an aerated polymer solution in an electric field. Multiple jets, which were a prerequisite for increasing the volume of production, were found in this electrospinning process. The morphology of the deposited fibers was straight, coiled and helix observed by a scanning electron microscope (SEM) and an optical microscopy. The results showed that the product of this process was similar to that of a traditional electrospinning process and illustrated a good prospect of application

Temperature dependent transport and dielectric properties of cadmium titanate nanofiber mats

Directory of Open Access Journals (Sweden)

Z. Imran

2013-03-01

Full Text Available We investigate electrical and dielectric properties of cadmium titanate (CdTiO3 nanofiber mats prepared by electrospinning. The nanofibers were polycrystalline having diameter ∼50 nm-200 nm, average length ∼100 μm and crystallite size ∼25 nm. Alternating current impedance measurements were carried out from 318 K – 498 K. The frequency of ac signal was varied from 2 – 105 Hz. The complex impedance plots revealed two depressed semicircular arcs indicating the bulk and interface contribution to overall electrical behavior of nanofiber mats. The bulk resistance was found to increase with decrease in temperature exhibiting typical semiconductor like behavior. The modulus analysis shows the non-Debye type conductivity relaxation in nanofiber mats. The ac conductivity spectrum obeyed the Jonscher power law. Analysis of frequency dependent ac conductivity revealed presence of the correlated barrier hopping (CBH in nanofiber mats over the entire temperature range.

Influence of Poly-(L-Lactic Acid Nanofiber Functionalization on Maximum Load, Young's Modulus, and Strain of Nanofiber Scaffolds Before and After Cultivation of Osteoblasts: An In Vitro Study

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Jürgen Paletta

2009-01-01

Full Text Available The aim of this study was to characterize the influence of functionalization of synthetic poly-(L-lactic acid (PLLA nanofibers on mechanical properties such as maximum load, elongation, and Young's modulus. Furthermore, the impact of osteoblast growth on the various nanofiber scaffolds stability was determined. Nanofiber matrices composed of PLLA, PLLA-collagen, or BMP-2–incorporated PLLA were produced from different solvents by electrospinning. Standardized test samples of each nanofiber scaffold were subjected to failure protocol before or after incubation in the presence of osteoblasts over a period of 22 days under osteoinductive conditions. PLLA nanofibers electrospun from hexafluoroisopropanol (HFIP showed a higher strain and tended to have increased maximum loads and Young's modulus compared to PLLA fibers spun from dichloromethane. In addition, they had a higher resistance during incubation in the presence of cells. Functionalization by incorporation of growth factors increased Young's modulus, independent of the solvent used. However, the incorporation of growth factors using the HFIP system resulted in a loss of strain. Similar results were observed when PLLA was blended with different ratios of collagen. Summarizing the results, this study indicates that different functionalization strategies influence the mechanical stability of PLLA nanofibers. Therefore, an optimization of nanofibers should not only account for the optimization of biological effects on cells, but also has to consider the stability of the scaffold.

Tolnaftate-Loaded PolyacrylateElectrospun Nanofibers for an Impressive Regimen on Dermatophytosis

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Shashi Kiran Misra

2017-11-01

Full Text Available Dermatophytosis, topical fungal infection is the most common cause of skin bug in the world, generally underestimated and ignored. It is commonly caused by immensely mortifying and keratinophilic fungal eukaryotes which invade keratinized tissues and generate different tinea diseases in Mediterranean countries. We herein fabricated nanofibers/scaffolds embedded with thiocarbamate derivative topical antifungal tolnaftatefor the first time to target the complete elimination of dermatophyte at the site of infection. In this regard, variable combinations of biocompatible Eudragit grades (ERL100 and ERS100 were selected to provide better adhesion on the site of dermatophytosis, ample absorption of exudates during treatment, and customized controlled drug release. Surface topography analysis indicated that the fabricated nanofibers were regular and defect-free, comprising distinct pockets with nanoscaled diameters. Characterization and compatibility studies of tolnaftate, polymers, and their nanofibers were performed through ATR-FTIR, TGA, and PXRD. Remarkable hydrophilicity and an excellent swelling index were obtained from a 3:1 ratio of ERL100/ERS100 electrospun D3 nanofibers, which is an essential benchmark for the fabrication of nanofibrous scaffolds for alleviating dermatophytosis. In vitro drug release investigation revealed that a nonwoven nanomesh of nanofibers could control the rate of drug release for 8 h. A microdilution assay exhibited inhibition of more than 95% viable cells of Trichophyton rubrum for 96 h. However, Microsporum species rigidly restricted the effect of bioactive antifungal nanofibers and hence showed resistance. In vivo activity on Trichophyton rubrum infected Swiss albino mice revealed complete inhibition of fungal pathogens on successive applications of D3 nanofibers for 7 days. This investigation suggests potential uses of tolnaftate loaded polyacrylate nanofibers as dressing materials/scaffolds for effective

Electrospun Fe3O4/TiO2 hybrid nanofibers and their in vitro biocompatibility: Prospective matrix for satellite cell adhesion and cultivation

International Nuclear Information System (INIS)

Amna, Touseef; Hassan, M. Shamshi; Van Ba, Hoa; Khil, Myung-Seob; Lee, Hak-Kyo; Hwang, I.H.

2013-01-01

We report the fabrication of novel Fe 3 O 4 /TiO 2 hybrid nanofibers with the improved cellular response for potential tissue engineering applications. In this study, Fe 3 O 4 /TiO 2 hybrid nanofibers were prepared by facile sol–gel electrospinning using titanium isopropoxide and iron(III) nitrate nonahydrate as precursors. The obtained electrospun nanofibers were vacuum dried at 80 °C and then calcined at 500 °C. The physicochemical characterization of the synthesized composite nanofibers was carried out by scanning electron microscopy, energy dispersive X-ray spectroscopy, transmission electron microscopy and X-ray diffraction pattern. To examine the in vitro cytotoxicity, satellite cells were treated with as-prepared Fe 3 O 4 /TiO 2 and the viability of cells was analyzed by Cell Counting Kit-8 assay at regular time intervals. The morphological features of unexposed satellite cells and exposed to Fe 3 O 4 /TiO 2 composite were examined with a phase contrast microscope whereas the quantification of cell viability was carried out via confocal laser scanning microscopy. The morphology of the cells attached to hybrid matrix was observed by Bio-SEM. Cytotoxicity experiments indicated that the satellite cells could attach to the Fe 3 O 4 /TiO 2 composite nanofibers after being cultured. We observed that Fe 3 O 4 –TiO 2 composite nanofibers could support cell adhesion and growth. Results from this study therefore suggest that Fe 3 O 4 /TiO 2 composite scaffold with small diameters (approximately 200 nm) can mimic the natural extracellular matrix well and provide possibilities for diverse applications in the field of tissue engineering and regenerative medicine. Highlights: ► We report fabrication of novel Fe 3 O 4 /TiO 2 hybrid nanofibers by facile electrospinning. ► The utilized satellite cells were isolated from native Korean Hanwoo cattle. ► Fe 3 O 4 /TiO 2 composite with small diameters (∼ 200 nm) can mimic the natural ECM well. ► Fe 3 O 4 /TiO 2

Chitosan based nanofibers in bone tissue engineering.

Science.gov (United States)

Balagangadharan, K; Dhivya, S; Selvamurugan, N

2017-11-01

Bone tissue engineering involves biomaterials, cells and regulatory factors to make biosynthetic bone grafts with efficient mineralization for regeneration of fractured or damaged bones. Out of all the techniques available for scaffold preparation, electrospinning is given priority as it can fabricate nanostructures. Also, electrospun nanofibers possess unique properties such as the high surface area to volume ratio, porosity, stability, permeability and morphological similarity to that of extra cellular matrix. Chitosan (CS) has a significant edge over other materials and as a graft material, CS can be used alone or in combination with other materials in the form of nanofibers to provide the structural and biochemical cues for acceleration of bone regeneration. Hence, this review was aimed to provide a detailed study available on CS and its composites prepared as nanofibers, and their associated properties found suitable for bone tissue engineering. Copyright © 2016 Elsevier B.V. All rights reserved.

Polyacrylonitrile Nanofiber-Based Quartz Crystal Microbalance for Sensitive Detection of Safrole

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Aditya Rianjanu

2018-04-01

Full Text Available Safrole is the main precursor for producing the amphetamine-type stimulant (ATS drug, N-methyl-3,4-methylenedioxyamphetamine (MDMA, also known as ecstasy. We devise a polyacrylonitrile (PAN nanofiber-based quartz crystal microbalance (QCM for detecting safrole. The PAN nanofibers were fabricated by direct electrospinning to modify the QCM chips. The PAN nanofiber on the QCM chips has a diameter of 240 ± 10 nm. The sensing of safrole by QCM modified with PAN nanofiber shows good reversibility and an apparent sensitivity of 4.6 Hz·L/mg. The proposed method is simple, inexpensive, and convenient for detecting safrole, and can be an alternative to conventional instrumental analytical methods for general volatile compounds.

Preparation, characterization of electrospun meso-hydroxylapatite nanofibers and their sorptions on Co(II)

Energy Technology Data Exchange (ETDEWEB)

Wang, Hualin, E-mail: hlwang@hfut.edu.cn [School of Chemical Technology, Hefei University of Technology, Hefei, Anhui 230009 (China); Zhang, Peng; Ma, Xingkong; Jiang, Suwei; Huang, Yan; Zhai, Linfeng [School of Chemical Technology, Hefei University of Technology, Hefei, Anhui 230009 (China); Jiang, Shaotong [School of Biotechnology and Food Engineering, Hefei University of Technology, Hefei, Anhui 230009 (China)

2014-01-30

Highlights: • PVA/HA nanofibers could change into meso-HA nanofibers by calcination process. • Sorption of Co(II) on meso-HA was strongly dependent on pH and ionic strength. • Sorption kinetic data were well fitted by the pseudo-second-order rate equation. • Sorption isotherms could be well described by the Langmuir model. • Sorption process of Co(II) on meso-HA nanofibers was spontaneous and endothermic. -- Abstract: In this work, mesoporous hydroxylapatite (meso-HA) nanofibers were prepared via calcination process with polyvinyl alcohol/HA (PVA/HA) hybrid nanofibers fabricated by electrospinning technique as precursors, and the removal efficiency of meso-HA nanofibers toward Co(II) was evaluated via sorption kinetics and sorption isotherms. Furthermore, the sorption behaviors of Co(II) on meso-HA nanofibers were explored as a function of pH, ionic strength, and thermodynamic parameters. There existed hydrogen bonds between HA and PVA matrix in precursor nanofibers which could change into meso-HA nanofibers with main pore diameter at 27 nm and specific surface area at 114.26 m{sup 2}/g by calcination process. The sorption of Co(II) on meso-HA was strongly dependent on pH and ionic strength. Outer-sphere surface complexation or ion exchange was the main mechanisms of Co(II) adsorption on meso-HA at low pH, whereas inner-sphere surface complexation was the main adsorption mechanism at high pH. The sorption kinetic data were well fitted by the pseudo-second-order rate equation. The sorption isotherms could be well described by the Langmuir model. The thermodynamic parameters (ΔH°, ΔS° and ΔG°) calculated from the temperature-dependent sorption isotherms suggested that the sorption process of Co(II) on meso-HA nanofibers was spontaneous and endothermic.

Ultra-High Density Single Nanometer-Scale Anodic Alumina Nanofibers Fabricated by Pyrophosphoric Acid Anodizing

Science.gov (United States)

Kikuchi, Tatsuya; Nishinaga, Osamu; Nakajima, Daiki; Kawashima, Jun; Natsui, Shungo; Sakaguchi, Norihito; Suzuki, Ryosuke O.

2014-12-01

Anodic oxide fabricated by anodizing has been widely used for nanostructural engineering, but the nanomorphology is limited to only two oxides: anodic barrier and porous oxides. Therefore, the discovery of an additional anodic oxide with a unique nanofeature would expand the applicability of anodizing. Here we demonstrate the fabrication of a third-generation anodic oxide, specifically, anodic alumina nanofibers, by anodizing in a new electrolyte, pyrophosphoric acid. Ultra-high density single nanometer-scale anodic alumina nanofibers (1010 nanofibers/cm2) consisting of an amorphous, pure aluminum oxide were successfully fabricated via pyrophosphoric acid anodizing. The nanomorphologies of the anodic nanofibers can be controlled by the electrochemical conditions. Anodic tungsten oxide nanofibers can also be fabricated by pyrophosphoric acid anodizing. The aluminum surface covered by the anodic alumina nanofibers exhibited ultra-fast superhydrophilic behavior, with a contact angle of less than 1°, within 1 second. Such ultra-narrow nanofibers can be used for various nanoapplications including catalysts, wettability control, and electronic devices.

Facile Synthesis of Porous Silicon Nanofibers by Magnesium Reduction for Application in Lithium Ion Batteries.

Science.gov (United States)

Cho, Daehwan; Kim, Moonkyoung; Hwang, Jeonghyun; Park, Jay Hoon; Joo, Yong Lak; Jeong, Youngjin

2015-12-01

We report a facile fabrication of porous silicon nanofibers by a simple three-stage procedure. Polymer/silicon precursor composite nanofibers are first fabricated by electrospinning, a water-based spinning dope, which undergoes subsequent heat treatment and then reduction using magnesium to be converted into porous silicon nanofibers. The porous silicon nanofibers are coated with a graphene by using a plasma-enhanced chemical vapor deposition for use as an anode material of lithium ion batteries. The porous silicon nanofibers can be mass-produced by a simple and solvent-free method, which uses an environmental-friendly polymer solution. The graphene-coated silicon nanofibers show an improved cycling performance of a capacity retention than the pure silicon nanofibers due to the suppression of the volume change and the increase of electric conductivity by the graphene.

Electrospun PBLG/PLA nanofiber membrane for constructing in vitro 3D model of melanoma.

Science.gov (United States)

Wang, Yaping; Qian, Junmin; Liu, Ting; Xu, Weijun; Zhao, Na; Suo, Aili

2017-07-01

Though much progress in utilizing tissue engineering technology to investigate tumor development in vitro has been made, the effective management of human melanoma is still a challenge in clinic due to lack of suitable 3D culture systems. In this study, we prepared a poly(γ-benzyl-l-glutamate)/poly(lactic acid) (PBLG/PLA) nanofiber membrane by electrospinning and demonstrated its suitability as a matrix for 3D culture of melanoma cells in vitro. The electrospun PBLG/PLA nanofiber membrane displayed a smooth and uniform fibrous morphology and had a desirable water contact angle of 79.3±0.6°. The average diameter of PBLG/PLA nanofibers was 320.3±95.1nm that was less than that (516.2±163.3nm) of pure PLA nanofibers. The addition of PBLG into PLA decreased the cold crystallization peak of PLA fibers from 93 to 75°C. The in vitro biocompatibility of PBLG/PLA nanofiber membrane was evaluated with B16F10 cells using PLA nanofiber membrane as control. It was found that, compared to PLA nanofiber membrane, PBLG/PLA nanofiber membrane could better support cell viability and proliferation, as indicated by MTT assay and live-dead staining. SEM results revealed that PBLG/PLA rather than PLA nanofiber membrane promoted the generation of tumoroid-like structures. These findings clearly demonstrated that the electrospun PBLG/PLA nanofiber membrane could mimick the extracellular matrix of melanoma microenvironment and be a promising platform for 3D cell culture. Copyright © 2017 Elsevier B.V. All rights reserved.

Fabricated nano-fiber diameter as liquid concentration sensors

Science.gov (United States)

Chyad, Radhi M.; Mat Jafri, Mohd Zubir; Ibrahim, Kamarulazizi

Nanofiber is characterized by thin, long, and very soft silica. Taper fibers are made using an easy and low cost chemical method. Etching is conducted with a HF solution to remove cladding and then a low molarity HF solution to reduce the fiber core diameter. One approach to on-line monitoring of the etching process uses spectrophotometer with a white light source. In the aforementioned technique, this method aims to determine the diameter of the reduced core and show the evolution of the two different processes from the nanofiber regime to the fixed regime in which the mode was remote from the surrounding evanescent field, intensity can propagate outside the segment fiber when the core diameter is less than 500 nm. Manufacturing technologies of nano-fiber sensors offer a number of approved properties of optical fiber sensors utilized in various sensory applications. The nano-fiber sensor is utilized to sense the difference in the concentration of D-glucose in double-distilled deionized water and to measure the refractive index (RI) of a sugar solution. Our proposed method exhibited satisfactory capability based on bimolecular interactions in the biological system. The response of the nano-fiber sensors indicates a different kind of interaction among various groups of AAs. These results can be interpreted in terms of solute-solute and solute-solvent interactions and the structure making or breaking ability of solutes in the given solution. This study utilized spectra photonics to measure the transmission of light through different concentrations of sugar solution, employing cell cumber and nano-optical fibers as sensors.

Electrospinning of Polyacrylonitrile Nanofibers and Simulation of Electric Field via Finite Element method

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Hadi Samadian

2017-04-01

Full Text Available Objective(s: Since the electric field is the main driving force in electrospinning systems, the modeling and analysis of electric field distribution are critical to the nanofibers production. The aim of this study was modeling of the electric field and investigating the various parameters on polyacrylonitrile (PAN nanofibers morphology and diameter. Methods: The electric field profile at the nozzle and electrospinning zone was evaluated by Finite Element Method. The morphology and diameter of nanofibers were examined by Scanning electron microscopy (SEM. Results: The results of the electric field analysis indicated that the electric field was concentrated at the tip of the nozzle. Moreover, in the spinning direction, the electric field was concentrated at the surface of the spinneret and decayed rapidly toward the surface of the collector. Increasing polymer solution concentration from 7 to 11wt.% led to increasing nanofibers diameter form 77.76 ± 19.44 to 202.42 ± 36.85. Conclusions: Base on our results, it could be concluded that concentration of the electric field at the tip of the nozzle is high and initiates jet and nanofibers formation. PAN nanofibers can be transformed to carbon nanofibers which have various applications in biomedicine.

Enhanced thermal conductance of polymer composites through embeddingaligned carbon nanofibers

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Dale K. Hensley

2016-07-01

Full Text Available The focus of this work is to find a more efficient method of enhancing the thermal conductance of polymer thin films. This work compares polymer thin films embedded with randomly oriented carbon nanotubes to those with vertically aligned carbon nanofibers. Thin films embedded with carbon nanofibers demonstrated a similar thermal conductance between 40–60 μm and a higher thermal conductance between 25–40 μm than films embedded with carbon nanotubes with similar volume fractions even though carbon nanotubes have a higher thermal conductivity than carbon nanofibers.

Preparation and Electrochemical Properties of Silver Doped Hollow Carbon Nanofibers

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LI Fu

2016-11-01

Full Text Available Silver doped PAN-based hollow carbon nanofibers were prepared combining co-electrospinning with in situ reduction technique subsequently heat treatment to improve the electrochemical performances of carbon based supercapacitor electrodes. The morphology, structure and electrochemical performances of the resulted nanofiber were studied. The results show that the silver nanoparticles can be doped on the surface of hollow carbon nanofibers and the addition of silver favors the improvement of the electrochemical performances, exhibiting the enhanced reversibility of electrode reaction and the capacitance and the reduced charge transfer impedance.

Modeling, simulation, and experiments of coating growth on nanofibers

International Nuclear Information System (INIS)

Clemons, C. B.; Hamrick, P.; Heminger, J.; Kreider, K. L.; Young, G. W.; Buldum, A.; Evans, E.; Zhang, G.

2008-01-01

This work is a comparison of modeling and simulation results with experiments for an integrated experimental/modeling investigation of a procedure to coat nanofibers and core-clad nanostructures with thin film materials using plasma enhanced physical vapor deposition. In the experimental effort, electrospun polymer nanofibers are coated with metallic materials under different operating conditions to observe changes in the coating morphology. The modeling effort focuses on linking simple models at the reactor level, nanofiber level and atomic level to form a comprehensive model. The comprehensive model leads to the definition of an evolution equation for the coating free surface around an isolated nanofiber. This evolution equation was previously derived and solved under conditions of a nearly circular coating, with a concentration field that was only radially dependent and that was independent of the location of the coating free surface. These assumptions permitted the development of analytical expressions for the concentration field. The present work does not impose the above-mentioned conditions and considers numerical simulations of the concentration field that couple with level set simulations of the evolution equation for the coating free surface. Further, the cases of coating an isolated fiber as well as a multiple fiber mat are considered. Simulation results are compared with experimental results as the reactor pressure and power, as well as the nanofiber mat porosity, are varied

Formation of high aspect ratio polyamide-6 nanofibers via electrically induced double layer during electrospinning

International Nuclear Information System (INIS)

Nirmala, R.; Nam, Ki Taek; Park, Soo-Jin; Shin, Yu-Shik; Navamathavan, R.; Kim, Hak Yong

2010-01-01

In the present study, the formation of high aspect ratio nanofibers in polyamide-6 was investigated as a function of applied voltage ranging from 15 to 25 kV using electrospinning technique. All other experimental parameters were kept constant. The electrospun polyamide-6 nanofibers were characterized by field-emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM) and matrix-assisted laser desorption ionization time-of-flight (MALDI-TOF). FE-SEM images of polyamide-6 nanofibers showed that the diameter of the electrospun fiber was decreased with increasing applied voltage. At the critical applied voltage, the polymer solution was completely ionized to form the dense high aspect ratio nanofibers in between the main nanofibers. The diameter of the polyamide-6 nanofibers was observed to be in the range of 75-110 nm, whereas the high aspect ratio structures consisted of regularly distributed very fine nanofibers with diameters of about 9-28 nm. Trends in fiber diameter and diameter distribution were discussed for the high aspect ratio nanofibers. TEM results revealed that the formation of double layers in polyamide-6 nanofibers and then split-up into ultrafine fibers. The electrically induced double layer in combination with the polyelectrolytic nature of solution is proposed as the suitable mechanisms for the formation of high aspect ratio nanofibers in polyamide-6.

Electrospun curcumin loaded poly(ε-caprolactone)/gum tragacanth nanofibers for biomedical application.

Science.gov (United States)

Ranjbar-Mohammadi, Marziyeh; Bahrami, S Hajir

2016-03-01

In this work curcumin (Cur)-loaded poly(ε-caprolactone) (PCL)/gum tragacanth (GT) scaffold membranes which provided the controlled release of curcumin for over 20 days were fabricated by electrospinning. Field Emission Scanning Electron Microscopy (FESEM) analysis, Fourier Transform Infrared Spectroscopy (FTIR) and differential scanning calorimetry (DSC) were applied to characterize the produced nanofibers. These nanofibers were evaluated for water absorption capacity, in vitro drug release, biodegradation test, cell culture and MTT analysis. The water contact angle measurements indicated that addition of GT and curcumin in composition resulted in increase in the hydrophilicity of the nanofibers. Biodegradation test for the fabricated nanofibers exhibited that PCL/GT, PCL/Cur-3% and PCL/GT/Cur-3% nanofibers preserved their structure after 15 days. The in vitro release profile of curcumin showed 6.86, 14 and 30.09% burst release for PCL/GT/Cur-1%, PCL/GT/Cur-3% and PCL/Cur-3% nanofibers respectively. The effect of curcumin concentration in the nanofibers composition on the cell viability was assessed by the MTS assay. The cytotoxic effect of released curcumin on the fibroblast cells was examined. The PCL/GT/Cur-3% with suitable mechanical properties, excellent biological characteristics, and maintaining their original structure in degradation media may have potential application as a wound dressing patch for healing slow rate wounds. Copyright © 2015 Elsevier B.V. All rights reserved.

Extraction of cellulose nanofibers from Pinus oocarpa residues

Energy Technology Data Exchange (ETDEWEB)

Manrich, Anny; Martins, Maria Alice, E-mail: anny@daad-alumni.de [EMBRAPA Instrumentacao, Sao Carlos, SP (Brazil); Moraes, Jheyce Cristina; Pasquoloto, Camila [Universidade Federal de Sao Carlos (UFSCar), SP (Brazil)

2016-07-01

Full text: Pinus oocarpa, which wood is moderately hard and tough, is planted in Brazil for reforestation and employed for timber production used in constructions. The wood residues, such as shavings, bark and sawdust represent 30% to 50% of the total volume of wood production, of which the sawdust is 10%{sup 1}. Cellulose nanofibers is nanomaterials having a diameter between 5 nm and 20 nm and a length of up to hundreds of nm. To obtain nanofibers from cellulose sources, such as sisal and sugarcane bagasse, is used chemical processes, in which the lignocellulosic material initially undergoes pre-treatments to promote partial separation of the cellulose, such as mercerisation and bleaching thus disposing lignin and hemicellulose components. Sequentially, by controlled acid hydrolysis, amorphous regions of the cellulose are removed, and crystalline cellulose is isolated in the form of cellulose nanofibers. In this work, nanofibers from sawdust of Pinnus oocarpa, containing 44.8 wt% of cellulose 20.6 wt% hemicellulose and 30.0 wt% insoluble lignin were isolated by mercerisation (NaOH 5%, 80°C, 120 min), followed by bleaching (NaOH + acetic acid + NaClO{sub 2}, 80 deg C, 240min) and acid hydrolysis (60 wt% sulfuric acid, 45 °C, 40min). Nanofibers obtained were characterized by DRX and SEM-FEG. Results showed that, for used conditions, fiber acid hydrolysis was not complete, therefore a biphasic suspension was formed. Crystallinity index achieved was not much higher than that from pinus fiber itself, increasing from 62% to 65% and signs of cellulose type II were observed. SEM images showed elongated fibers, which have diameter of 15 ± 5 nm and length of hundreds of nm, what means that they have a large L/D aspect ratio. Nanofiber extraction yield was very low (1.3 wt% of initial residue). All steps of the process are being reviewed aiming at better results. 1) Morais, S. A. L.; Nascimento E. A. e D. C. Melo, 2005, R. Árvore, 29, 3, 461-470. (author)

Graft polymerization of acrylic acid onto chitin nanofiber to improve dispersibility in basic water.

Science.gov (United States)

Ifuku, Shinsuke; Iwasaki, Masayoshi; Morimoto, Minoru; Saimoto, Hiroyuki

2012-09-01

Graft copolymerization of acrylic acid (AA) on chitin nanofibers was carried out with potassium persulfate as a free radical initiator in an aqueous medium. The molar ratio of grafted AA increased with the AA concentration. The grafted chitin nanofibers were characterized by FT-IR, FE-SEM, UV-vis, XRD, and TGA. After polymerization, the characteristic morphology of chitin nanofibers was maintained. Chitin nanofibers grafted with AA were efficiently dissociated and dispersed homogeneously in basic water because of the electrostatic repulsion effect between nanofibers. AA was grafted on the surface and amorphous part of chitin nanofibers, and the original crystalline structure of α-chitin was maintained. At 330 °C, the weight residue of the graft copolymer increased with the grafted AA content. Copyright © 2012 Elsevier Ltd. All rights reserved.

Electrospun polyvinyl alcohol–collagen–hydroxyapatite nanofibers: a biomimetic extracellular matrix for osteoblastic cells

International Nuclear Information System (INIS)

Song Wei; Shi Tong; Ren Weiping; Markel, David C; Wang Sunxi; Mao Guangzhao

2012-01-01

The failure of prosthesis after total joint replacement is due to the lack of early implant osseointegration. In this study polyvinyl alcohol–collagen–hydroxyapatite (PVA-Col-HA) electrospun nanofibrous meshes were fabricated as a biomimetic bone-like extracellular matrix for the modification of orthopedic prosthetic surfaces. In order to reinforce the PVA nanofibers, HA nanorods and Type I collagen were incorporated into the nanofibers. We investigated the morphology, biodegradability, mechanical properties and biocompatibility of the prepared nanofibers. Our results showed these inorganic–organic blended nanofibers to be degradable in vitro. The encapsulated nano-HA and collagen interacted with the PVA content, reinforcing the hydrolytic resistance and mechanical properties of nanofibers that provided longer lasting stability. The encapsulated nano-HA and collagen also enhanced the adhesion and proliferation of murine bone cells (MC3T3) in vitro. We propose the PVA-Col-HA nanofibers might be promising modifying materials on implant surfaces for orthopedic applications. (paper)

Electrical properties of in-situ grown and transferred organic nanofibers

DEFF Research Database (Denmark)

Oliveira Hansen, Roana Melina de; Madsen, Morten; Kjelstrup-Hansen, Jakob

2010-01-01

Para-hexaphenylene (p6P) molecules have the ability to self-assemble into organic nanofibers, which exhibit a range of interesting optical and optoelectronic properties such as intense, polarized luminescence, waveguiding and lasing. The nanofibers are typically grown on specific single...

Improved infiltration of stem cells on electrospun nanofibers

International Nuclear Information System (INIS)

Shabani, Iman; Haddadi-Asl, Vahid; Seyedjafari, Ehsan; Babaeijandaghi, Farshad; Soleimani, Masoud

2009-01-01

Nanofibrous scaffolds have been recently used in the field of tissue engineering because of their nano-size structure which promotes cell attachment, function, proliferation and infiltration. In this study, nanofibrous polyethersulfone (PES) scaffolds was prepared via electrospinning. The scaffolds were surface modified by plasma treatment and collagen grafting. The surface changes then investigated by contact angle measurements and FTIR-ATR. The results proved grafting of the collagen on nanofibers surface and increased hydrophilicity after plasma treatment and collagen grafting. The cell interaction study was done using stem cells because of their ability to differentiate to different kinds of cell lines. The cells had normal morphology on nanofibers and showed very high infiltration through collagen grafted PES nanofibers. This infiltration capability is very useful and needed to make 3D scaffolds in tissue engineering.

Branched carbon nanofiber network synthesis at room temperature using radio frequency supported microwave plasmas

OpenAIRE

Boskovic, BO; Stolojan, V; Zeze, DA; Forrest, RD; Silva, SRP; Haq, S

2004-01-01

Carbon nanofibers have been grown at room temperature using a combination of radio frequency and microwave assisted plasma-enhanced chemical vapor deposition. The nanofibers were grown, using Ni powder catalyst, onto substrates kept at room temperature by using a purposely designed water-cooled sample holder. Branched carbon nanofiber growth was obtained without using a template resulting in interconnected carbon nanofiber network formation on substrates held at room temperatur...

Perspectives: Nanofibers and nanowires for disordered photonics

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Dario Pisignano

2017-03-01

Full Text Available As building blocks of microscopically non-homogeneous materials, semiconductor nanowires and polymer nanofibers are emerging component materials for disordered photonics, with unique properties of light emission and scattering. Effects found in assemblies of nanowires and nanofibers include broadband reflection, significant localization of light, strong and collective multiple scattering, enhanced absorption of incident photons, synergistic effects with plasmonic particles, and random lasing. We highlight recent related discoveries, with a focus on material aspects. The control of spatial correlations in complex assemblies during deposition, the coupling of modes with efficient transmission channels provided by nanofiber waveguides, and the embedment of random architectures into individually coded nanowires will allow the potential of these photonic materials to be fully exploited, unconventional physics to be highlighted, and next-generation optical devices to be achieved. The prospects opened by this technology include enhanced random lasing and mode-locking, multi-directionally guided coupling to sensors and receivers, and low-cost encrypting miniatures for encoders and labels.

Composite nanofibers for highly efficient photocatalytic degradation of organic dyes from contaminated water

Energy Technology Data Exchange (ETDEWEB)

Mohamed, Alaa [Department of Materials and NanoPhysics, Royal Institute of Technology (KTH), 16440 Kista, Stockholm (Sweden); Mechanical Design and Production Engineering Department, Cairo University, 12613 Giza (Egypt); Production Engineering and Printing Technology Department, Akhbar El Yom Academy, 12655 Giza (Egypt); El-Sayed, Ramy [Experimental Cancer Medicine, KFC, Novum, Department of laboratory Medicine, Karolinska Institute, 14186 Stockholm (Sweden); Osman, T.A. [Mechanical Design and Production Engineering Department, Cairo University, 12613 Giza (Egypt); Toprak, M.S.; Muhammed, M. [Department of Materials and NanoPhysics, Royal Institute of Technology (KTH), 16440 Kista, Stockholm (Sweden); Uheida, A., E-mail: salam@kth.se [Department of Materials and NanoPhysics, Royal Institute of Technology (KTH), 16440 Kista, Stockholm (Sweden)

2016-02-15

In this study highly efficient photocatalyst based on composite nanofibers containing polyacrylonitrile (PAN), carbon nanotubes (CNT), and surface functionalized TiO{sub 2} nanoparticles was developed. The composite nanofibers were fabricated using electrospinning technique followed by chemical crosslinking. The surface modification and morphology changes of the fabricated composite nanofibers were examined through SEM, TEM, and FTIR analysis. The photocatalytic performance of the composite nanofibers for the degradation of model molecules, methylene blue and indigo carmine, under UV irradiation in aqueous solutions was investigated. The results demonstrated that high photodegradation efficiency was obtained in a short time and at low power intensity compared to other reported studies. The effective factors on the degradation of the dyes, such as the amount of catalyst, solution pH and irradiation time were investigated. The experimental kinetic data were fitted using pseudo-first order model. The effect of the composite nanofibers as individual components on the degradation efficiency of MB and IC was evaluated in order to understand the overall photodegradation mechanism. The results obtained showed that all the components possess significant effect on the photodegradation activity of the composite nanofibers. The stability studies demonstrated that the photodegradation efficiency can remain constant at the level of 99% after five consecutive cycles. - Highlights: • Develop effective photocatalyst based on PAN–CNT/TiO{sub 2}–NH{sub 2} composite nanofibers. • High photodegradation efficiency and fast kinetics was obtained. • Regeneration of the composite nanofibers allowed the reuse of these material. • Mechanism of the photocatalytic degradation was proposed. • The flexibility of the composite nanofibers allows use in a continuous operation mode.

Composite nanofibers for highly efficient photocatalytic degradation of organic dyes from contaminated water

International Nuclear Information System (INIS)

Mohamed, Alaa; El-Sayed, Ramy; Osman, T.A.; Toprak, M.S.; Muhammed, M.; Uheida, A.

2016-01-01

In this study highly efficient photocatalyst based on composite nanofibers containing polyacrylonitrile (PAN), carbon nanotubes (CNT), and surface functionalized TiO 2 nanoparticles was developed. The composite nanofibers were fabricated using electrospinning technique followed by chemical crosslinking. The surface modification and morphology changes of the fabricated composite nanofibers were examined through SEM, TEM, and FTIR analysis. The photocatalytic performance of the composite nanofibers for the degradation of model molecules, methylene blue and indigo carmine, under UV irradiation in aqueous solutions was investigated. The results demonstrated that high photodegradation efficiency was obtained in a short time and at low power intensity compared to other reported studies. The effective factors on the degradation of the dyes, such as the amount of catalyst, solution pH and irradiation time were investigated. The experimental kinetic data were fitted using pseudo-first order model. The effect of the composite nanofibers as individual components on the degradation efficiency of MB and IC was evaluated in order to understand the overall photodegradation mechanism. The results obtained showed that all the components possess significant effect on the photodegradation activity of the composite nanofibers. The stability studies demonstrated that the photodegradation efficiency can remain constant at the level of 99% after five consecutive cycles. - Highlights: • Develop effective photocatalyst based on PAN–CNT/TiO 2 –NH 2 composite nanofibers. • High photodegradation efficiency and fast kinetics was obtained. • Regeneration of the composite nanofibers allowed the reuse of these material. • Mechanism of the photocatalytic degradation was proposed. • The flexibility of the composite nanofibers allows use in a continuous operation mode.

Iodine doping effects on the lattice thermal conductivity of oxidized polyacetylene nanofibers

Energy Technology Data Exchange (ETDEWEB)

Bi, Kedong, E-mail: lishi@mail.utexas.edu, E-mail: kedongbi@seu.edu.cn [Jiangsu Key Laboratory for Design and Manufacture of Micro-Nano Biomedical Instruments, School of Mechanical Engineering, Southeast University, Nanjing 211189 (China); Department of Mechanical Engineering, University of Texas at Austin, Austin, Texas 78712 (United States); Weathers, Annie; Pettes, Michael T.; Shi, Li, E-mail: lishi@mail.utexas.edu, E-mail: kedongbi@seu.edu.cn [Department of Mechanical Engineering, University of Texas at Austin, Austin, Texas 78712 (United States); Matsushita, Satoshi; Akagi, Kazuo [Department of Polymer Chemistry, Kyoto University, Kyoto 615-8510 (Japan); Goh, Munju [Department of Polymer Chemistry, Kyoto University, Kyoto 615-8510 (Japan); Institute of Advanced Composite Materials, Korea Institute of Science and Technology (KIST), Eunha-ri san 101, Bondong-eup, Wanju-gun, Jeolabuk-do 565-905 (Korea, Republic of)

2013-11-21

Thermal transport in oxidized polyacetylene (PA) nanofibers with diameters in the range between 74 and 126 nm is measured with the use of a suspended micro heater device. With the error due to both radiation and contact thermal resistance corrected via a differential measurement procedure, the obtained thermal conductivity of oxidized PA nanofibers varies in the range between 0.84 and 1.24 W m{sup −1} K{sup −1} near room temperature, and decreases by 40%–70% after iodine doping. It is also found that the thermal conductivity of oxidized PA nanofibers increases with temperature between 100 and 350 K. Because of exposure to oxygen during sample preparation, the PA nanofibers are oxidized to be electrically insulating before and after iodine doping. The measurement results reveal that iodine doping can result in enhanced lattice disorder and reduced lattice thermal conductivity of PA nanofibers. If the oxidation issue can be addressed via further research to increase the electrical conductivity via doping, the observed suppressed lattice thermal conductivity in doped polymer nanofibers can be useful for the development of such conducting polymer nanostructures for thermoelectric energy conversion.

Electrospinning of functional poly(methyl methacrylate) nanofibers containing cyclodextrin-menthol inclusion complexes

Energy Technology Data Exchange (ETDEWEB)

Uyar, Tamer; Besenbacher, Flemming [Interdisciplinary Nanoscience Center (iNANO), Aarhus University, DK-8000, Aarhus C (Denmark); Nur, Yusuf; Hacaloglu, Jale [Department of Chemistry, Middle East Technical University, Ankara, 06530 (Turkey)], E-mail: tamer@inano.dk, E-mail: tamer@unam.bilkent.edu.tr

2009-03-25

Electrospinning of nanofibers with cyclodextrin inclusion complexes (CD-ICs) is particularly attractive since distinct properties can be obtained by combining the nanofibers with specific functions of the CD-ICs. Here we report on the electrospinning of poly(methyl methacrylate) (PMMA) nanofibers containing cyclodextrin-menthol inclusion complexes (CD-menthol-ICs). These CD-menthol-IC functionalized nanofibers were developed with the purpose of producing functional nanofibers that contain fragrances/flavors with high temperature stability, and menthol was used as a model fragrance/flavor material. The PMMA nanofibers were electrospun with CD-menthol-ICs using three type of CD: {alpha}-CD, {beta}-CD, and {gamma}-CD. Direct pyrolysis mass spectrometry (DP-MS) studies showed that the thermal evaporation of menthol occurred over a very high and a broad temperature range (100-355 deg. C) for PMMA/CDmenthol-IC nanowebs, demonstrating the complexation of menthol with the CD cavity and its high temperature stability. Furthermore, as the size of CD cavity increased in the order {alpha}-CD<{beta}-CD<{gamma}-CD, the thermal evolution of menthol shifted to higher temperatures, suggesting that the strength of interaction between menthol and the CD cavity is in the order {gamma}-CD>{beta}-CD>{alpha}-CD.

Preparation and characterization of oriented poly(vinyl alcohol)/carbon nanotube composite nanofibers

Science.gov (United States)

Shimizu, Akikazu; Kato, Hayato; Sato, Taiga; Kushida, Masahito

2017-07-01

Oriented nanofiber mats blended with carbon nanotubes (CNTs) are expected to be applied as cell seeding scaffolds. Biomaterials that are often used for cell seeding scaffolds generally have low mechanical strength and low electrical conductivity; thus, it has been difficult to apply them to tissues such as heart and nerve. In this study, we prepared oriented poly(vinyl alcohol) (PVA) nanofiber mats blended with various CNT concentrations (up to 10 wt %) by electrospinning using the parallel plate electrodes as collectors with applied voltage. The morphology, mechanical properties, and electrical properties of the prepared oriented nanofiber mats were measured by using various techniques such as scanning electron microscopy (SEM). The tensile strength of the oriented nanofiber mats in the applied voltage direction increased from 2.5 to 9.7 MPa with CNT concentration. Furthermore, the electrical conductivity of the oriented nanofiber mats in the applied voltage direction increased from 0.67 × 10-7 to 4.3 × 10-7 S·m-1. Also, the mechanical strength and electrical conductivity of the oriented nanofiber mats in the applied voltage direction were 3-4 and 2-3 times higher than those in the perpendicular direction, respectively.

Iodine doping effects on the lattice thermal conductivity of oxidized polyacetylene nanofibers

International Nuclear Information System (INIS)

Bi, Kedong; Weathers, Annie; Pettes, Michael T.; Shi, Li; Matsushita, Satoshi; Akagi, Kazuo; Goh, Munju

2013-01-01

Thermal transport in oxidized polyacetylene (PA) nanofibers with diameters in the range between 74 and 126 nm is measured with the use of a suspended micro heater device. With the error due to both radiation and contact thermal resistance corrected via a differential measurement procedure, the obtained thermal conductivity of oxidized PA nanofibers varies in the range between 0.84 and 1.24 W m −1  K −1 near room temperature, and decreases by 40%–70% after iodine doping. It is also found that the thermal conductivity of oxidized PA nanofibers increases with temperature between 100 and 350 K. Because of exposure to oxygen during sample preparation, the PA nanofibers are oxidized to be electrically insulating before and after iodine doping. The measurement results reveal that iodine doping can result in enhanced lattice disorder and reduced lattice thermal conductivity of PA nanofibers. If the oxidation issue can be addressed via further research to increase the electrical conductivity via doping, the observed suppressed lattice thermal conductivity in doped polymer nanofibers can be useful for the development of such conducting polymer nanostructures for thermoelectric energy conversion

Coaxial electrospun polyurethane core-shell nanofibers for shape memory and antibacterial nanomaterials

Directory of Open Access Journals (Sweden)

2011-02-01

Full Text Available A novel kind of shape memory polyurethane (SMPU nanofibers with core-shell nanostructure is fabricated using coaxial electrospinning. Transmission electron microscopy (TEM and scanning electron microscopy (SEM results show that nanofibers with core-shell structure or bead-on-string structure can be electrospun successfully from the core solution of polycaprolactone based SMPU (CLSMPU and shell solution of pyridine containing polyurethane (PySMPU. In addition to the excellent shape memory effect with good shape fixity, excellent antibacterial activity against both gramnegative bacteria and gram-positive bacteria are achieved in the CLSMPU-PySMPU core-shell nanofiber. Finally, it is proposed that the antibacterial mechanism should be resulted from the PySMPU shell materials containing amido group in γ position and the high surface area per unit mass of nanofibers. Thus, the CLSMPU-PySMPU core shell nanofibers can be used as both shape memory nanomaterials and antibacterial nanomaterials.

Effects of Schwann cell alignment along the oriented electrospun chitosan nanofibers on nerve regeneration.

Science.gov (United States)

Wang, Wei; Itoh, Soichiro; Konno, Katsumi; Kikkawa, Takeshi; Ichinose, Shizuko; Sakai, Katsuyoshi; Ohkuma, Tsuneo; Watabe, Kazuhiko

2009-12-15

We have constructed a chitosan nonwoven nanofiber mesh tube consisting of oriented fibers by the electrospinning method. The efficacy of oriented nanofibers on Schwann cell alignment and positive effect of this tube on peripheral nerve regeneration were confirmed. The physical properties of the chitosan nanofiber mesh sheets prepared by electrospinning with or without fiber orientation were characterized. Then, immortalized Schwann cells were cultured on these sheets. Furthermore, the chitosan nanofiber mesh tubes with or without orientation, and bilayered chitosan mesh tube with an inner layer of oriented nanofibers and an outer layer of randomized nanofibers were bridgegrafted into rat sciatic nerve defect. As a result of fiber orientation, the tensile strength along the axis of the sheet increased. Because Schwann cells aligned along the nanofibers, oriented fibrous sheets could exhibit a Schwann cell column. Functional recovery and electrophysiological recovery occurred in time in the oriented group as well as in the bilayered group, and approximately matched those in the isograft. Furthermore, histological analysis revealed that the sprouting of myelinated axons occurred vigorously followed by axonal maturation in the isograft, oriented, and bilayered group in the order. The oriented chitosan nanofiber mesh tube may be a promising substitute for autogenous nerve graft.

Fabrication of a novel aluminum surface covered by numerous high-aspect-ratio anodic alumina nanofibers

Science.gov (United States)

Nakajima, Daiki; Kikuchi, Tatsuya; Natsui, Shungo; Sakaguchi, Norihito; Suzuki, Ryosuke O.

2015-11-01

The formation behavior of anodic alumina nanofibers via anodizing in a concentrated pyrophosphoric acid under various conditions was investigated using electrochemical measurements and SEM/TEM observations. Pyrophosphoric acid anodizing at 293 K resulted in the formation of numerous anodic alumina nanofibers on an aluminum substrate through a thin barrier oxide and honeycomb oxide with narrow walls. However, long-term anodizing led to the chemical dissolution of the alumina nanofibers. The density of the anodic alumina nanofibers decreased as the applied voltage increased in the 10-75 V range. However, active electrochemical dissolution of the aluminum substrate occurred at a higher voltage of 90 V. Low temperature anodizing at 273 K resulted in the formation of long alumina nanofibers measuring several micrometers in length, even though a long processing time was required due to the low current density during the low temperature anodizing. In contrast, high temperature anodizing easily resulted in the formation and chemical dissolution of alumina nanofibers. The structural nanofeatures of the anodic alumina nanofibers were controlled by choosing of the appropriate electrochemical conditions, and numerous high-aspect-ratio alumina nanofibers (>100) can be successfully fabricated. The anodic alumina nanofibers consisted of a pure amorphous aluminum oxide without anions from the employed electrolyte.

Dynamic stability of nano-fibers self-assembled from short amphiphilic A6D peptides.

Science.gov (United States)

Nikoofard, Narges; Maghsoodi, Fahimeh

2018-04-07

Self-assembly of A 6 D amphiphilic peptides in explicit water is studied by using coarse-grained molecular dynamics simulations. It is observed that the self-assembly of randomly distributed A 6 D peptides leads to the formation of a network of nano-fibers. Two other simulations with cylindrical nano-fibers as the initial configuration show the dynamic stability of the self-assembled nano-fibers. As a striking feature, notable fluctuations occur along the axes of the nano-fibers. Depending on the number of peptides per unit length of the nano-fiber, flat-shaped bulges or spiral shapes along the nano-fiber axis are observed at the fluctuations. Analysis of the particle distribution around the nano-fiber indicates that the hydrophobic core and the hydrophilic shell of the nano-structure are preserved in both simulations. The size of the deformations and their correlation times are different in the two simulations. This study gives new insights into the dynamics of the self-assembled nano-structures of short amphiphilic peptides.

Dynamic stability of nano-fibers self-assembled from short amphiphilic A6D peptides

Science.gov (United States)

Nikoofard, Narges; Maghsoodi, Fahimeh

2018-04-01

Self-assembly of A6D amphiphilic peptides in explicit water is studied by using coarse-grained molecular dynamics simulations. It is observed that the self-assembly of randomly distributed A6D peptides leads to the formation of a network of nano-fibers. Two other simulations with cylindrical nano-fibers as the initial configuration show the dynamic stability of the self-assembled nano-fibers. As a striking feature, notable fluctuations occur along the axes of the nano-fibers. Depending on the number of peptides per unit length of the nano-fiber, flat-shaped bulges or spiral shapes along the nano-fiber axis are observed at the fluctuations. Analysis of the particle distribution around the nano-fiber indicates that the hydrophobic core and the hydrophilic shell of the nano-structure are preserved in both simulations. The size of the deformations and their correlation times are different in the two simulations. This study gives new insights into the dynamics of the self-assembled nano-structures of short amphiphilic peptides.

Ag loading induced visible light photocatalytic activity for pervoskite SrTiO3 nanofibers

Science.gov (United States)

Wu, Yeqiu; He, Tao

2018-06-01

The synthesis and photocatalytic activities of Ag-SrTiO3 nanofibers were reported in this work. The fabricated Ag-SrTiO3 nanofibers were characterized by TG-DSC, XRD, IR, XPS, SEM, TEM, DRS and ESR techniques. The XRD and IR results show that Ag-SrTiO3 nanofibers have a perovskite structure after the heat treatment at 700 °C. The XPS result shows that Ag element exists as Ag0 in the fabricated Ag-SrTiO3 nanofibers. The SEM and TEM images indicate the obtaining of nanofibers with porous structure. The photocatalytic activity of Ag-SrTiO3 nanofibers was evaluated by degrading RhB and MB under visible light irradiation. The Ag-SrTiO3 nanofibers show excellent photocatalytic activity under visible light irradiation because of the surface plasmon resonance effect of Ag0. In the photocatalysis process of RhB and MB, lots of hydroxyl radicals were generated, which plays the key role in the decomposition of organic pollutants.

Uniaxially aligned ceramic nanofibers obtained by chemical mechanical processing

Energy Technology Data Exchange (ETDEWEB)

Tararam, R. [Univ Estadual Paulista – UNESP – Instituto de Química, Rua Prof. Francisco Degni n° 55, CEP 14800-900 Araraquara, SP (Brazil); Foschini, C.R. [Univ Estadual Paulista – UNESP – Faculdade de Engenharia de Bauru, Dept. de Eng. Mecanica, Av. Eng. Luiz Edmundo C. Coube 14-01, CEP 17033-360 Bauru, SP (Brazil); Destro, F.B. [Univ Estadual Paulista – UNESP – Faculdade de Engenharia de Guaratinguetá, Guaratinguetá 12516-410, SP (Brazil); Simões, A.Z., E-mail: alezipo@yahoo.com [Univ Estadual Paulista – UNESP – Faculdade de Engenharia de Guaratinguetá, Guaratinguetá 12516-410, SP (Brazil); Longo, E.; Varela, J.A. [Univ Estadual Paulista – UNESP – Instituto de Química, Rua Prof. Francisco Degni n° 55, CEP 14800-900 Araraquara, SP (Brazil)

2014-08-01

For this study, we investigated a simple method to generate well aligned nanofibers over large areas using an organic polymer stretched over the substrate surface With this method, ZnO and CuO 3D parallel nanowire arrays were successfully prepared by calcinations of the polymer fibers. X-ray diffraction (XRD) analysis revealed that the copper oxide has a monoclinic structure while the zinc oxide has a hexagonal structure. Scanning electron microscopy (SEM) analysis showed ceramic nanofibers with an average diameter of 120 nm which were composed of small nanoparticles which are 10 nm in diameter. The ability to obtain uniaxially aligned nanofibers reveals a range of interesting properties with potential applications for sensors, catalysts and energy technologies.

Vorinostat-eluting poly(DL-lactide-co-glycolide) nanofiber-coated stent for inhibition of cholangiocarcinoma cells.

Science.gov (United States)

Kwak, Tae Won; Lee, Hye Lim; Song, Yeon Hui; Kim, Chan; Kim, Jungsoo; Seo, Sol-Ji; Jeong, Young-Il; Kang, Dae Hwan

2017-01-01

The aim of this study was to fabricate a vorinostat (Zolinza™)-eluting nanofiber membrane-coated gastrointestinal (GI) stent and to study its antitumor activity against cholangiocarcinoma (CCA) cells in vitro and in vivo. Vorinostat and poly(DL-lactide-co-glycolide) dissolved in an organic solvent was sprayed onto a GI stent to make a nanofiber-coated stent using an electro-spinning machine. Intact vorinostat and vorinostat released from nanofibers was used to assess anticancer activity in vitro against various CCA cells. The antitumor activity of the vorinostat-eluting nanofiber membrane-coated stent was evaluated using HuCC-T1 bearing mice. A vorinostat-incorporated polymer nanofiber membrane was formed on the surface of the GI stent. Vorinostat was continuously released from the nanofiber membrane over 10 days, and its release rate was higher in cell culture media than in phosphate-buffered saline. Released vorinostat showed similar anticancer activity against various CCA cells in vitro compared to that of vorinostat. Like vorinostat, vorinostat released from nanofibers induced acetylation of histone H4 and inhibited histone deacetylases 1⋅3⋅4/5/7 expression in vitro and in vivo. Furthermore, vorinostat nanofibers showed a higher tumor growth inhibition rate in HuCC-T1 bearing mice than vorinostat injections. Vorinostat-eluting nanofiber membranes showed significant antitumor activity against CCA cells in vitro and in vivo. We suggest the vorinostat nanofiber-coated stent may be a promising candidate for CCA treatment.

Electrospinning and characterization of polyamide 66 nanofibers with different molecular weights

Directory of Open Access Journals (Sweden)

Lilia Muller Guerrini

2009-06-01

Full Text Available Polyamide 66 (PA66 nanofibers of different molecular weights were obtained by electrospinning of formic acid solutions. An ionic salt, NaCl, was also added to the solutions to increase the conductivity. PA66 concentrations between 15-17 wt.(%/v and electrical fields between 2.0 and 2.5 kV/cm were the best conditions to produce the smallest nanofibers; however, the addition of NaCl increased the fibers average diameters.The characterization of the fibers was done by scanning electron microscopy (SEM, differential scanning calorimetry (DSC, wide angle X rays diffraction (WAXD and Fourier Transformed Infrared (FTIR. As the molecular weight decreased, the nanofibers average diameters also decreased; however, critical number average and weight average molecular weights were necessary for electrospinning. As the amounts of carboxyl terminal groups (CTG increased, the nanofibers average diameters decreased; however, above CTG's critical values of 8.7 x 10-5 mol.g-1 no electrospinning was possible. The addition of ionic salt increased the electrical conductivity of the solutions and increased the nanofibers' average diameters. By DSC, residual solvent in all the electrospun mats was found; two melting endotherms, one between 248 and 258 °C and the other one between 258 and 267 °C, depending on the sample were also observed. These endotherms were attributed to the melting, re-crystallization and re-melting of the PA66 α-phase. The nanofibers had low % of crystallinity compared to a textile fiber. By WAXS and FTIR, confirmation of the presence of α-phase crystals, of small dimensions and highly imperfect and of a very small amount of β and γ-phases crystals in the nanofibers structure was obtained.

Chitosan nanofibers for transbuccal insulin delivery.

Science.gov (United States)

Lancina, Michael G; Shankar, Roopa Kanakatti; Yang, Hu

2017-05-01

In this work, they aimed at producing chitosan based nanofiber mats capable of delivering insulin via the buccal mucosa. Chitosan was electrospun into nanofibers using poly(ethylene oxide) (PEO) as a carrier molecule in various feed ratios. The mechanical properties and degradation kinetics of the fibers were measured. Insulin release rates were determined in vitro using an ELISA assay. The bioactivity of released insulin was measured in terms of Akt activation in pre-adipocytes. Insulin permeation across the buccal mucosa was measured in an ex-vivo porcine transbuccal model. Fiber morphology, mechanical properties, and in vitro stability were dependent on PEO feed ratio. Lower PEO content blends produced smaller diameter fibers with significantly faster insulin release kinetics. Insulin showed no reduction in bioactivity due to electrospinning. Buccal permeation of insulin facilitated by high chitosan content blends was significantly higher than that of free insulin. Taken together, the work demonstrates that chitosan-based nanofibers have the potential to serve as a transbuccal insulin delivery vehicle. © 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 105A: 1252-1259, 2017. © 2017 Wiley Periodicals, Inc.

Preparations, properties and applications of chitosan based nanofibers fabricated by electrospinning

Directory of Open Access Journals (Sweden)

2011-04-01

Full Text Available Chitosan is soluble in most acids. The protonation of the amino groups on the chitosan backbone inhibits the electrospinnability of pure chitosan. Recently, electrospinning of nanofibers based on chitosan has been widely researched and numerous nanofibers containing chitosan have been prepared by decreasing the number of the free amino groups of chitosan as the nanofibiers have enormous possibilities for better utilization in various areas. This article reviews the preparations and properties of the nanofibers which were electrospun from pure chitosan, blends of chitosan and synthetic polymers, blends of chitosan and protein, chitosan derivatives, as well as blends of chitosan and inorganic nanoparticles, respectively. The applications of the nanofibers containing chitosan such as enzyme immobilization, filtration, wound dressing, tissue engineering, drug delivery and catalysis are also summarized in detail.

Bioresorbable nanofiber-based systems for wound healing and drug delivery: optimization of fabrication parameters.

Science.gov (United States)

Katti, Dhirendra S; Robinson, Kyle W; Ko, Frank K; Laurencin, Cato T

2004-08-15

Wound healing is a complex process that often requires treatment with antibiotics. This article reports the initial development of a biodegradable polymeric nanofiber-based antibiotic delivery system. The functions of such a system would be (a) to serve as a biodegradable gauze, and (b) to serve as an antibiotic delivery system. The polymer used in this study was poly(lactide-co-glycolide) (PLAGA), and nanofibers of PLAGA were fabricated with the use of the electrospinning process. The objective of this study was to determine the effect of fabrication parameters: orifice diameter (needle gauge), polymer solution concentration, and voltage per unit length, on the morphology and diameter of electrospun nanofibers. The needle gauges studied were 16 (1.19 mm), 18 (0.84 mm), and 20 (0.58 mm), and the range of polymer solution concentration studied was from 0.10 g/mL to 0.30 g/mL. The effect of voltage was determined by varying the voltage per unit electrospinning distance, and the range studied was from 0.375 kV/cm to 1.5 kV/cm. In addition, the mass per unit area of the electrospun nanofibers as a function of time was determined and the feasibility of antibiotic (cefazolin) loading into the nanofibers was also studied. The results indicate that the diameter of nanofibers decreased with an increase in needle gauge (decrease in orifice diameter), and increased with an increase in the concentration of the polymer solution. The voltage study demonstrated that the average diameter of the nanofibers decreased with an increase in voltage. However, the effect of voltage on fiber diameter was less pronounced as compared to polymer solution concentration. The results of the areal density study indicated that the mass per unit area of the electrospun nanofibers increased linearly with time. Feasibility of drug incorporation into the nanofibers was demonstrated with the use of cefazolin, a broad-spectrum antibiotic. Overall, these studies demonstrated that PLAGA nanofibers can be

Improvement of air permeability of Bubbfil nanofiber membrane

Directory of Open Access Journals (Sweden)

Wang Fei-Yan

2018-01-01

Full Text Available Nanofiber membranes always have extremely high filter efficiency and remarkably low pressure drop. In order to further improve air permeability of bubbfil nanofiber membranes, the plasma technology is used for surface treatment in this paper. The results show that plasma treatment can improve air permeability by 4.45%. Under higher power plasma treatment, earthworm like etchings are produced on the membrane surface with fractal dimensions of about 1.138.

Magnetic porous PtNi/SiO2 nanofibers for catalytic hydrogenation of p-nitrophenol

Science.gov (United States)

Guan, Huijuan; Chao, Cong; Kong, Weixiao; Hu, Zonggao; Zhao, Yafei; Yuan, Siguo; Zhang, Bing

2017-06-01

In this work, the mesoporous SiO2 nanofibers from pyrolyzing precursor of electrospun nanofibers were employed as support to immobilize PtNi nanocatalyst (PtNi/SiO2 nanofibers). AFM, XRD, SEM, TEM, XPS, ICP-AES and N2 adsorption/desorption analysis were applied to systematically investigate the morphology and microstructure of as-prepared products. Results showed that PtNi alloy nanoparticles with average diameter of 18.7 nm were formed and could be homogeneously supported on the surface of porous SiO2 nanofiber, which further indicated that the SiO2 nanofibers with well-developed porous structure, large specific surface area, and roughened surface was a benefit for the support of PtNi alloy nanoparticles. The PtNi/SiO2 nanofibers catalyst exhibited an excellent catalytic activity towards the reduction of p-nitrophenol, and the catalyst's kinetic parameter ( k n = 434 × 10-3 mmol s-1 g-1) was much higher than those of Ni/SiO2 nanofibers (18 × 10-3 mmol s-1 g-1), Pt/SiO2 nanofibers (55 × 10-3 mmol s-1 g-1) and previous reported PtNi catalysts. The catalyst could be easily recycled from heterogeneous reaction system based on its good magnetic properties (the Ms value of 11.48 emu g-1). In addition, PtNi/SiO2 nanofibers also showed an excellent stability and the conversion rate of p-nitrophenol still could maintain 94.2% after the eighth using cycle.

Novel tumor-targeting, self-assembling peptide nanofiber as a carrier for effective curcumin delivery

Directory of Open Access Journals (Sweden)

Liu J

2013-12-01

Full Text Available Jianfeng Liu, Jinjian Liu, Hongyan Xu, Yumin Zhang, Liping Chu, Qingfen Liu, Naling Song, Cuihong YangTianjin Key Laboratory of Molecular Nuclear Medicine, Institute of Radiation Medicine, Chinese Academy of Medical Science and Peking Union Medical College, People's Republic of ChinaAbstract: The poor aqueous solubility and low bioavailability of curcumin restrict its clinical application for cancer treatment. In this study, a novel tumor-targeting nanofiber carrier was developed to improve the solubility and tumor-targeting ability of curcumin using a self-assembled Nap-GFFYG-RGD peptide. The morphologies of the peptide nanofiber and the curcumin-encapsulated nanofiber were visualized by transmission electron microscopy. The tumor-targeting activity of the curcumin-encapsulated Nap-GFFYG-RGD peptide nanofiber (f-RGD-Cur was studied in vitro and in vivo, using Nap-GFFYG-RGE peptide nanofiber (f-RGE-Cur as the control. Curcumin was encapsulated into the peptide nanofiber, which had a diameter of approximately 10–20 nm. Curcumin showed sustained-release behavior from the nanofibers in vitro. f-RGD-Cur showed much higher cellular uptake in αvβ3 integrin-positive HepG2 liver carcinoma cells than did non-targeted f-RGE-Cur, thereby leading to significantly higher cytotoxicity. Ex vivo studies further demonstrated that curcumin could accumulate markedly in mouse tumors after administration of f-RGD-Cur via the tail vein. These results indicate that Nap-GFFYG-RGD peptide self-assembled nanofibers are a promising hydrophobic drug delivery system for targeted treatment of cancer.Keywords: nanofiber, tumor-targeting, self-assembling, curcumin, drug delivery

Surface modification of polyvinyl alcohol/malonic acid nanofibers by gaseous dielectric barrier discharge plasma for glucose oxidase immobilization

International Nuclear Information System (INIS)

Afshari, Esmail; Mazinani, Saeedeh; Ranaei-Siadat, Seyed-Omid; Ghomi, Hamid

2016-01-01

Highlights: • We fabricated polyvinyl alcohol/malonic acid nanofibers using electrospinning. • The surface nanofibers were modified by gaseous (air, nitrogen, CO_2 and argon) dielectric barrier discharge. • Among them, air plasma had the most significant effect on glucose oxidase immobilization. • Chemical analysis showed that after modification of nanofibers by air plasma, the carboxyl group increased. • After air plasma treatment, reusability and storage stability of glucose oxidase immobilized on nanofibers improved. - Abstract: Polymeric nanofiber prepares a suitable situation for enzyme immobilization for variety of applications. In this research, we have fabricated polyvinyl alcohol (PVA)/malonic acid nanofibers using electrospinning. After fabrication of nanofibers, the effect of air, nitrogen, CO_2, and argon DBD (dielectric barrier discharge) plasmas on PVA/malonic acid nanofibers were analysed. Among them, air plasma had the most significant effect on glucose oxidase (GOx) immobilization. Attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectrum analysis and X-ray photoelectron spectroscopy (XPS) results revealed that in case of air plasma modified nanofibers, the carboxyl groups on the surface are increased. The scanning electron microscopy (SEM) images showed that, after GOx immobilization, the modified nanofibers with plasma has retained its nanofiber structure. Finally, we analysed reusability and storage stability of GOx immobilized on plasma modified and unmodified nanofibers. The results were more satisfactory for modified nanofibers with respect to unmodified ones.

Surface modification of polyvinyl alcohol/malonic acid nanofibers by gaseous dielectric barrier discharge plasma for glucose oxidase immobilization

Energy Technology Data Exchange (ETDEWEB)

Afshari, Esmail, E-mail: e.afshari@mail.sbu.ac.ir [Laser and Plasma Research Institute, Shahid Beheshti University, Evin, 1983963113 Tehran (Iran, Islamic Republic of); Mazinani, Saeedeh [Amirkabir Nanotechnology Research Institute (ANTRI), Amirkabir University of Technology, 15875-4413, Tehran (Iran, Islamic Republic of); Ranaei-Siadat, Seyed-Omid [Protein Research Center, Shahid Beheshti University, Evin, 1983963113 Tehran (Iran, Islamic Republic of); Ghomi, Hamid [Laser and Plasma Research Institute, Shahid Beheshti University, Evin, 1983963113 Tehran (Iran, Islamic Republic of)

2016-11-01

Highlights: • We fabricated polyvinyl alcohol/malonic acid nanofibers using electrospinning. • The surface nanofibers were modified by gaseous (air, nitrogen, CO{sub 2} and argon) dielectric barrier discharge. • Among them, air plasma had the most significant effect on glucose oxidase immobilization. • Chemical analysis showed that after modification of nanofibers by air plasma, the carboxyl group increased. • After air plasma treatment, reusability and storage stability of glucose oxidase immobilized on nanofibers improved. - Abstract: Polymeric nanofiber prepares a suitable situation for enzyme immobilization for variety of applications. In this research, we have fabricated polyvinyl alcohol (PVA)/malonic acid nanofibers using electrospinning. After fabrication of nanofibers, the effect of air, nitrogen, CO{sub 2}, and argon DBD (dielectric barrier discharge) plasmas on PVA/malonic acid nanofibers were analysed. Among them, air plasma had the most significant effect on glucose oxidase (GOx) immobilization. Attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectrum analysis and X-ray photoelectron spectroscopy (XPS) results revealed that in case of air plasma modified nanofibers, the carboxyl groups on the surface are increased. The scanning electron microscopy (SEM) images showed that, after GOx immobilization, the modified nanofibers with plasma has retained its nanofiber structure. Finally, we analysed reusability and storage stability of GOx immobilized on plasma modified and unmodified nanofibers. The results were more satisfactory for modified nanofibers with respect to unmodified ones.

Function of NaOH hydrolysis in electrospinning ZnO nanofibers via using polylactide as templates

International Nuclear Information System (INIS)

Liu, Mengzhu; Wang, Yongpeng; Cheng, Zhiqiang; Song, Lihua; Zhang, Mingyue; Hu, Meijuan; Li, Junfeng

2014-01-01

Graphical abstract: - Highlights: • PLA was used as templates to electrospin ZnO nanofibers for the first time. • Without NaOH hydrolysis, only ZnO film was prepared. • Under function of NaOH, ZnO nanofibers were obtained. • The function of NaOH was discussed. • ZnO nanofibers showed much higher photocatalytical efficiency than ZnO film. - Abstract: Mixture of polylactide (8 wt%), zinc acetate (6 wt%) and hexafluoroisopropanol was first used as electrospinning solution to fabricate ZnO nanofibers. Unfortunately, after direct calcination of the precursor polylactide/zinc acetate nanofibers, only ZnO film was prepared. Surprisingly, when the precursor fibers were pre-hydrolyzed with NaOH, ZnO nanofibers with diameter of 678 nm were obtained. The mechanism analysis showed that the preserve of fiber structure was attributed to the formation of zinc polylactic acid in the process of hydrolyzation. After characterized by scanning electron microscope and transmission electron microscope, the ZnO film was found to be an aggregation of irregular nanoparticles and the ZnO nanofiber was a necklace-like arrangement of cylindrical grains. X-ray diffraction and photoluminescence measurements indicated that the crystalline quality of the ZnO nanofibers was higher than the film. Furthermore, photocatalytic performance of the ZnO samples was investigated. Comparing with ZnO film, ZnO nanofibers exhibited much higher activity

Ultrasound-assisted preparation of electrospun carbon nanofiber/graphene composite electrode for supercapacitors

Science.gov (United States)

Dong, Qiang; Wang, Gang; Hu, Han; Yang, Juan; Qian, Bingqing; Ling, Zheng; Qiu, Jieshan

2013-12-01

Electrospun carbon nanofiber/graphene (CNF/G) composites are prepared by in situ electrospinning polymeric nanofibers with simultaneous spraying graphene oxide, followed by heat treatment. The freestanding carbon nanofiber web acts as a framework for sustaining graphene, which helps to prevent the agglomeration of graphene and to provide a high conductivity for the efficient charge transfer to the pores. The as-obtained CNF/G composite exhibits a specific capacitance of 183 F g-1, which is approximately 1.6 times higher than that of the pristine CNF. The results have demonstrated that the high performance of the CNF/G composite is due to the novel structure and the synergic effect of graphene and the carbon nanofibers.

Physicochemical investigations of carbon nanofiber supported Cu/ZrO{sub 2} catalyst

Energy Technology Data Exchange (ETDEWEB)

Din, Israf Ud, E-mail: drisraf@yahoo.com, E-mail: maizats@petronas.com.my; Shaharun, Maizatul S., E-mail: drisraf@yahoo.com, E-mail: maizats@petronas.com.my [Department of Fundamental and Applied Sciences, Universiti Teknologi PETRONAS (Malaysia); Subbarao, Duvvuri, E-mail: duvvuri-subbarao@petronas.com.my [Department of Chemical Engineering, Universiti Teknologi PETRONAS (Malaysia); Naeem, A., E-mail: naeeem64@yahoo.com [National Centre of Excellence in Physical Chemistry, University of Peshawar (Pakistan)

2014-10-24

Zirconia-promoted copper/carbon nanofiber catalysts (Cu‐ZrO{sub 2}/CNF) were prepared by the sequential deposition precipitation method. The Herringbone type of carbon nanofiber GNF-100 (Graphite nanofiber) was used as a catalyst support. Carbon nanofiber was oxidized to (CNF-O) with 5% and 65 % concentration of nitric acid (HNO{sub 3}). The CNF activated with 5% HNO{sub 3} produced higher surface area which is 155 m{sup 2}/g. The catalyst was characterized by X-ray Diffraction (XRD), Fourier Transform Infra-Red (FTIR) and N{sub 2} adsorption-desorption. The results showed that increase of HNO{sub 3} concentration reduced the surface area and porosity of the catalyst.

Enhanced photoluminescence of Si nanocrystals-doped cellulose nanofibers by plasmonic light scattering

Energy Technology Data Exchange (ETDEWEB)

Sugimoto, Hiroshi [Department of Electrical and Computer Engineering and Photonics Center, Boston University, 8 Saint Mary Street, Boston, Massachusetts 02215 (United States); Department of Electrical and Electronic Engineering, Graduate School of Engineering, Kobe University, Rokkodai, Nada, Kobe 657-8501 (Japan); Zhang, Ran [Division of Materials Science and Engineering, Boston University, 15 Saint Mary' s Street, Brookline, Massachusetts 02446 (United States); Reinhard, Björn M. [Department of Chemistry and Photonics Center, Boston University, Boston, Massachusetts 02215 (United States); Fujii, Minoru [Department of Electrical and Electronic Engineering, Graduate School of Engineering, Kobe University, Rokkodai, Nada, Kobe 657-8501 (Japan); Perotto, Giovanni; Marelli, Benedetto; Omenetto, Fiorenzo G. [Department of Biomedical Engineering and Department of Physics, Tufts University, 4 Colby Street, Medford, Massachusetts 02155 (United States); Dal Negro, Luca, E-mail: dalnegro@bu.edu [Department of Electrical and Computer Engineering and Photonics Center, Boston University, 8 Saint Mary Street, Boston, Massachusetts 02215 (United States); Division of Materials Science and Engineering, Boston University, 15 Saint Mary' s Street, Brookline, Massachusetts 02446 (United States)

2015-07-27

We report the development of bio-compatible cellulose nanofibers doped with light emitting silicon nanocrystals and Au nanoparticles via facile electrospinning. By performing photoluminescence (PL) spectroscopy as a function of excitation wavelength, we demonstrate plasmon-enhanced PL by a factor of 2.2 with negligible non-radiative quenching due to plasmon-enhanced scattering of excitation light from Au nanoparticles to silicon nanocrystals inside the nanofibers. These findings provide an alternative approach for the development of plasmon-enhanced active systems integrated within the compact nanofiber geometry. Furthermore, bio-compatible light-emitting nanofibers prepared by a cost-effective solution-based processing are very promising platforms for biophotonic applications such as fluorescence sensing and imaging.

High Throughput Preparation of Aligned Nanofibers Using an Improved Bubble-Electrospinning

Directory of Open Access Journals (Sweden)

Liang Yu

2017-11-01

Full Text Available An improved bubble-electrospinning, consisting of a cone shaped air nozzle, a copper solution reservoir connected directly to the power generator, and a high speed rotating copper wire drum as a collector, was presented successfully to obtain high throughput preparation of aligned nanofibers. The influences of drum rotation speed on morphology and properties of obtained nanofibers were explored and researched. The results showed that the alignment degree, diameter distribution, and properties of nanofibers were improved with the increase of the drum rotation speed.

Osteoinductive peptide-functionalized nanofibers with highly ordered structure as biomimetic scaffolds for bone tissue engineering.

Science.gov (United States)

Gao, Xiang; Zhang, Xiaohong; Song, Jinlin; Xu, Xiao; Xu, Anxiu; Wang, Mengke; Xie, Bingwu; Huang, Enyi; Deng, Feng; Wei, Shicheng

2015-01-01

The construction of functional biomimetic scaffolds that recapitulate the topographical and biochemical features of bone tissue extracellular matrix is now of topical interest in bone tissue engineering. In this study, a novel surface-functionalized electrospun polycaprolactone (PCL) nanofiber scaffold with highly ordered structure was developed to simulate the critical features of native bone tissue via a single step of catechol chemistry. Specially, under slightly alkaline aqueous solution, polydopamine (pDA) was coated on the surface of aligned PCL nanofibers after electrospinning, followed by covalent immobilization of bone morphogenetic protein-7-derived peptides onto the pDA-coated nanofiber surface. Contact angle measurement, Raman spectroscopy, and X-ray photoelectron spectroscopy confirmed the presence of pDA and peptides on PCL nanofiber surface. Our results demonstrated that surface modification with osteoinductive peptides could improve cytocompatibility of nanofibers in terms of cell adhesion, spreading, and proliferation. Most importantly, Alizarin Red S staining, quantitative real-time polymerase chain reaction, immunostaining, and Western blot revealed that human mesenchymal stem cells cultured on aligned nanofibers with osteoinductive peptides exhibited enhanced osteogenic differentiation potential than cells on randomly oriented nanofibers. Furthermore, the aligned nanofibers with osteoinductive peptides could direct osteogenic differentiation of human mesenchymal stem cells even in the absence of osteoinducting factors, suggesting superior osteogenic efficacy of biomimetic design that combines the advantages of osteoinductive peptide signal and highly ordered nanofibers on cell fate decision. The presented peptide-decorated bone-mimic nanofiber scaffolds hold a promising potential in the context of bone tissue engineering.

Force and time-dependent self-assembly, disruption and recovery of supramolecular peptide amphiphile nanofibers.

Science.gov (United States)

Dikecoglu, F Begum; Topal, Ahmet E; Ozkan, Alper D; Tekin, E Deniz; Tekinay, Ayse B; Guler, Mustafa O; Dana, Aykutlu

2018-07-13

Biological feedback mechanisms exert precise control over the initiation and termination of molecular self-assembly in response to environmental stimuli, while minimizing the formation and propagation of defects through self-repair processes. Peptide amphiphile (PA) molecules can self-assemble at physiological conditions to form supramolecular nanostructures that structurally and functionally resemble the nanofibrous proteins of the extracellular matrix, and their ability to reconfigure themselves in response to external stimuli is crucial for the design of intelligent biomaterials systems. Here, we investigated real-time self-assembly, deformation, and recovery of PA nanofibers in aqueous solution by using a force-stabilizing double-pass scanning atomic force microscopy imaging method to disrupt the self-assembled peptide nanofibers in a force-dependent manner. We demonstrate that nanofiber damage occurs at tip-sample interaction forces exceeding 1 nN, and the damaged fibers subsequently recover when the tip pressure is reduced. Nanofiber ends occasionally fail to reconnect following breakage and continue to grow as two individual nanofibers. Energy minimization calculations of nanofibers with increasing cross-sectional ellipticity (corresponding to varying levels of tip-induced fiber deformation) support our observations, with high-ellipticity nanofibers exhibiting lower stability compared to their non-deformed counterparts. Consequently, tip-mediated mechanical forces can provide an effective means of altering nanofiber integrity and visualizing the self-recovery of PA assemblies.

Improvement of Polylactide Properties through Cellulose Nanocrystals Embedded in Poly(Vinyl Alcohol) Electrospun Nanofibers.

Science.gov (United States)

López de Dicastillo, Carol; Garrido, Luan; Alvarado, Nancy; Romero, Julio; Palma, Juan Luis; Galotto, Maria Jose

2017-05-11

Electrospun nanofibers of poly (vinyl alcohol) (PV) were obtained to improve dispersion of cellulose nanocrystals (CNC) within hydrophobic biopolymeric matrices, such as poly(lactic acid) (PLA). Electrospun nanofibers (PV/CNC) n were successfully obtained with a final concentration of 23% ( w / w ) of CNC. Morphological, structural and thermal properties of developed CNC and electrospun nanofibers were characterized. X-ray diffraction and thermal analysis revealed that the crystallinity of PV was reduced by the electrospinning process, and the incorporation of CNC increased the thermal stability of biodegradable nanofibers. Interactions between CNC and PV polymer also enhanced the thermal stability of CNC and improved the dispersion of CNC within the PLA matrix. PLA materials with CNC lyophilized were also casted in order to compare the properties with materials based on CNC containing nanofibers. Nanofibers and CNC were incorporated into PLA at three concentrations: 0.5%, 1% and 3% (CNC respect to polymer weight) and nanocomposites were fully characterized. Overall, nanofibers containing CNC positively modified the physical properties of PLA materials, such as the crystallinity degree of PLA which was greatly enhanced. Specifically, materials with 1% nanofiber 1PLA(PV/CNC) n presented highest improvements related to mechanical and barrier properties; elongation at break was enhanced almost four times and the permeation of oxygen was reduced by approximately 30%.

Preparation and luminescence properties of terbium-doped lanthanum oxide nanofibers by electrospinning

Energy Technology Data Exchange (ETDEWEB)

Song Lixin; Du Pingfan [Key Laboratory of Advanced Textile Materials and Manufacturing Technology (Zhejiang Sci-Tech University), Ministry of Education, Hangzhou 310018 (China); Xiong Jie, E-mail: jxiong@zstu.edu.cn [Key Laboratory of Advanced Textile Materials and Manufacturing Technology (Zhejiang Sci-Tech University), Ministry of Education, Hangzhou 310018 (China); Fan Xiaona; Jiao Yuxue [Key Laboratory of Advanced Textile Materials and Manufacturing Technology (Zhejiang Sci-Tech University), Ministry of Education, Hangzhou 310018 (China)

2012-01-15

Terbium-doped lanthanum oxide (La{sub 2}O{sub 3}:Tb{sup 3+}) nanofibers were prepared by electrospinning followed by calcination at high temperature. Thermogravimetric analyzer (TGA), field emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), and photoluminescence (PL) were used to characterize the obtained fibers. The results reveal that the nanofibers have an average diameter of ca. 95{+-}25 nm and are composed of pure La{sub 2}O{sub 3} phase. Under the excitation of 274 nm light, the La{sub 2}O{sub 3}:Tb{sup 3+} nanofibers exhibit the characteristic emission resulting from the {sup 5}D{sub 4}{yields}{sup 7}F{sub J} (J=3, 4, 5, 6) transitions of Tb{sup 3+} ions. And the PL emission intensity is stronger than that of their nanoparticle counterparts. - Highlights: > Tb{sup 3+}-doped La{sub 2}O{sub 3} (La{sub 2}O{sub 3}:Tb{sup 3+}) fluorescent nanofibers were prepared via a simple electrospinning technique. > Luminescent properties and other characteristics of the nanofibers were investigated in details. > Potential applications of La{sub 2}O{sub 3}:Tb{sup 3+} nanofibers and electrospinning technique described in this paper are suggested.

Fabrication and Characterization of Aligned Flexible Lead-Free Piezoelectric Nanofibers for Wearable Device Applications

Directory of Open Access Journals (Sweden)

Sang Hyun Ji

2018-03-01

Full Text Available Flexible lead-free piezoelectric nanofibers, based on BNT-ST (0.78Bi0.5Na0.5TiO3-0.22SrTiO3 ceramic and poly(vinylidene fluoride-trifluoroethylene (PVDF-TrFE copolymers, were fabricated by an electrospinning method and the effects of the degree of alignment in the nanofibers on the piezoelectric characteristics were investigated. The microstructure of the lead-free piezoelectric nanofibers was observed by field emission scanning electron microscope (FE-SEM and the orientation was analyzed by fast Fourier transform (FFT images. X-ray diffraction (XRD analysis confirmed that the phase was not changed by the electrospinning process and maintained a perovskite phase. Polarization-electric field (P-E loops and piezoresponse force microscopy (PFM were used to investigate the piezoelectric properties of the piezoelectric nanofibers, according to the degree of alignment—the well aligned piezoelectric nanofibers had higher piezoelectric properties. Furthermore, the output voltage of the aligned lead-free piezoelectric nanofibers was measured according to the vibration frequency and the bending motion and the aligned piezoelectric nanofibers with a collector rotation speed of 1500 rpm performed the best.

Dehydration driven changes in the structure and mechanical behavior of electrospun poly (vinyl alcohol) nanofibers

International Nuclear Information System (INIS)

Bansal, Ankita; Sinha, Arvind

2012-01-01

Electrospun nanofibers of poly (vinyl alcohol) (PVA) are well known for their possible application in different fields, ranging from packaging to tissue engineering. However, biomedical application of these nanofibers gets limited due to its rapid disintegration in water, causing mechanical instability. Addressing this issue, the present manuscript reports ethanol induced dehydration of electrospun PVA nanofibers, and its effects on the structure and mechanical properties of the electrospun system. A systematic variation in the structure and mechanical stability of nanofibers as a function of PVA concentration has also been established in the both hydrated and dehydrated states. - Highlights: ► Study reports structure-property correlation of dehydrated PVA nanofibers. ► Results confirm symmetrical reversal of properties in two states. ► Experimental results are in confirmation with the fusion model of nanofibers.

Polyaniline emeraldine base nanofibers as a radiostabilizing agent for PMMA

International Nuclear Information System (INIS)

Araujo, Patricia L.B.; Ferreira, Carlas C.; Araujo, Elmo S.

2007-01-01

Polyaniline (PANI) presents antioxidant and radical-scavenging properties. Substances having these characteristics are good candidates for radioprotecting agents. Some studies have also shown results pointing out to biocompatibility and biodegradability of PANI. These characteristics are desirable for substances in contact with biological tissues and have important implications for inclusion of PANI in physical mixtures with conventional radiosterilizable polymers. In this work, nanofibers of polyaniline emeraldine doped with (±)-camphor-10-sulfonic acid (PANI-(±)-CSA) were prepared by self-assembly method. Polyaniline emeraldine base (PANI-EB) nanofibers were obtained after dedoping with NH 4 OH and used as additives in films of commercial poly (methyl methacrylate) (PMMA). In order to assess possible radiostabilizing effects of PANI-EB and its aniline monomer (An) on the PMMA matrix, films containing 0.075 and 0.15% (wt/wt) of these substances were submitted to gamma irradiation from 25 to 75 kGy doses. Variation on viscosity-average molar mass (Mv) of the PMMA matrix at 25 kGy dose showed that samples containing An and PANI-EB nanofibers in amounts of 0.15% (wt/wt) underwent less degradation than control sample. When nanofibers were used as additives, no measurable variation of Mv could be detected in PMMA samples at this dose. At 75 kGy, all composites containing PANI-EB nanofibers underwent less degradation than control samples, suggesting that these additives are able to retain their action at doses higher than standard sterilization dose. These evidences show that PANI-EB nanofibers could be useful additives in commercial PMMA used in medical applications. FTIR spectroscopic characterization and scanning electron microscopy (SEM) of PANI samples were also performed. (author)

Mechanical characterization of TiO{sub 2} nanofibers produced by different electrospinning techniques

Energy Technology Data Exchange (ETDEWEB)

Vahtrus, Mikk [Institute of Physics, University of Tartu, Ravila 14c, 50412 Tartu (Estonia); Šutka, Andris [Institute of Physics, University of Tartu, Ravila 14c, 50412 Tartu (Estonia); Institute of Silicate Materials, Riga Technical University, P. Valdena 3/7, Riga LV-1048 (Latvia); Institute of Technical Physics, Riga Technical University, P. Valdena 3, Riga LV-1048 (Latvia); Vlassov, Sergei, E-mail: vlassovs@ut.ee [Institute of Solid State Physics, University of Latvia, Kengaraga 8, LV-1063 Riga (Latvia); Šutka, Anna [Institute of Textile Technology and Design, Riga Technical University, Riga LV-1048 (Latvia); Laboratory of Biomass Eco-Efficient Conversation, Latvian State Institute of Wood Chemistry, Dzerbenes Street 27, Riga LV-1006 (Latvia); Polyakov, Boris [Institute of Solid State Physics, University of Latvia, Kengaraga 8, LV-1063 Riga (Latvia); Saar, Rando; Dorogin, Leonid; Lõhmus, Rünno [Institute of Physics, University of Tartu, Ravila 14c, 50412 Tartu (Estonia); Materials Technologies Competence Centre, Riia 185b, 51014 Tartu (Estonia)

2015-02-15

In this work TiO{sub 2} nanofibers produced by needle and needleless electrospinning processes from the same precursor were characterized and compared using Raman spectroscopy, transmission electron microscopy (TEM), scanning electron microscopy (SEM) and in situ SEM nanomechanical testing. Phase composition, morphology, Young's modulus and bending strength values were found. Weibull statistics was used to evaluate and compare uniformity of mechanical properties of nanofibers produced by two different methods. It is shown that both methods yield nanofibers with very similar properties. - Graphical abstract: Display Omitted - Highlights: • TiO{sub 2} nanofibers were produced by needle and needleless electrospinning processes. • Structure was studied by Raman spectroscopy and electron microscopy methods. • Mechanical properties were measured using advanced in situ SEM cantilevered beam bending technique. • Both methods yield nanofibers with very similar properties.

The application of electrospun titania nanofibers in dye-sensitized solar cells.

Science.gov (United States)

Krysova, Hana; Zukal, Arnost; Trckova-Barakova, Jana; Chandiran, Aravind Kumar; Nazeeruddin, Mohammad Khaja; Grätzel, Michael; Kavan, Ladislav

2013-01-01

Titania nanofibers were fabricated using the industrial Nanospider(TM) technology. The preparative protocol was optimized by screening various precursor materials to get pure anatase nanofibers. Composite films were prepared by mixing a commercial paste of nanocrystalline anatase particles with the electrospun nanofibers, which were shortened by milling. The composite films were sensitized by Ru-bipyridine dye (coded C106) and the solar conversion efficiency was tested in a dye-sensitized solar cell filled with iodide-based electrolyte solution (coded Z960). The solar conversion efficiency of a solar cell with the optimized composite electrode (η = 7.53% at AM 1.5 irradiation) outperforms that of a solar cell with pure nanoparticle film (η = 5.44%). Still larger improvement was found for lower light intensities. At 10% sun illumination, the best composite electrode showed η = 7.04%, referenced to that of pure nanoparticle film (η = 4.69%). There are non-monotonic relations between the film's surface area, dye sorption capacity and solar performance of nanofiber-containing composite films, but the beneficial effect of the nanofiber morphology for enhancement of the solar efficiency has been demonstrated.

Ultra-Fast Degradation of Chemical Warfare Agents Using MOF-Nanofiber Kebabs.

Science.gov (United States)

Zhao, Junjie; Lee, Dennis T; Yaga, Robert W; Hall, Morgan G; Barton, Heather F; Woodward, Ian R; Oldham, Christopher J; Walls, Howard J; Peterson, Gregory W; Parsons, Gregory N

2016-10-10

The threat associated with chemical warfare agents (CWAs) motivates the development of new materials to provide enhanced protection with a reduced burden. Metal-organic frame-works (MOFs) have recently been shown as highly effective catalysts for detoxifying CWAs, but challenges still remain for integrating MOFs into functional filter media and/or protective garments. Herein, we report a series of MOF-nanofiber kebab structures for fast degradation of CWAs. We found TiO 2 coatings deposited via atomic layer deposition (ALD) onto polyamide-6 nanofibers enable the formation of conformal Zr-based MOF thin films including UiO-66, UiO-66-NH 2 , and UiO-67. Cross-sectional TEM images show that these MOF crystals nucleate and grow directly on and around the nanofibers, with strong attachment to the substrates. These MOF-functionalized nanofibers exhibit excellent reactivity for detoxifying CWAs. The half-lives of a CWA simulant compound and nerve agent soman (GD) are as short as 7.3 min and 2.3 min, respectively. These results therefore provide the earliest report of MOF-nanofiber textile composites capable of ultra-fast degradation of CWAs. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Fabrication and Characterization of Electrospun Wool Keratin/Poly(vinyl alcohol) Blend Nanofibers

OpenAIRE

Shuai Li; Xu-Hong Yang

2014-01-01

Wool keratin/poly(vinyl alcohol) (PVA) blend nanofibers were fabricated using the electrospinning method in formic acid solutions with different weight ratios of keratin to PVA. The resultant blend nanofibers were characterized by scanning electron microscopy (SEM), Fourier transform infrared (FTIR), X-ray diffraction (XRD), thermal gravimetric analysis (TGA), and tensile test. SEM images showed that the diameter of the blend nanofibers was affected by the content of keratin in blend solution...

In-situ synthesis of nanofibers with various ratios of BiOCl{sub x}/BiOBr{sub y}/BiOI{sub z} for effective trichloroethylene photocatalytic degradation

Energy Technology Data Exchange (ETDEWEB)

Zhang, Yifan [Department of Chemistry, Inha University, 100 Inharo, Incheon 402-751 (Korea, Republic of); Park, Mira [Department of Organic Materials and Fiber Engineering, Chonbuk National University, Jeonju 561-756 (Korea, Republic of); Kim, Hak Yong [Department of BIN Convergence Technology, Chonbuk National University, Jeonju, 561-756 (Korea, Republic of); Ding, Bin [College of Textiles, Donghua University, Shanghai 201620 (China); Park, Soo-Jin, E-mail: sjpark@inha.ac.kr [Department of Chemistry, Inha University, 100 Inharo, Incheon 402-751 (Korea, Republic of)

2016-10-30

Highlights: • BiOCl{sub x}/BiOBr{sub y}/BiOI{sub z}/PAN fibers were synthesized by in-situ method. • Photodegradation behavior of BiOCl{sub x}/BiOBr{sub y}/BiOI{sub z}/PAN fibers was measured under solar light irradiation. • BiOCl{sub 0.3}/BiOBr{sub 0.3}/BiOI{sub 0.4}/PAN fibers exhibited the highest photocatalytic activity. • Photocatalytic mechanism was discussed in detail. - Abstract: In this work, BiOCl{sub x}/BiOBr{sub y}/BiOI{sub z} (x + y + z = 1) composite nanofibers were prepared through electrospinning and the sol-gel methods. Photocatalytic degradation of trichloroethylene (TCE) by BiOCl{sub x}/BiOBr{sub y}/BiOI{sub z}/PAN nanofibers was systematically investigated via gas chromatography (GC). Optimum photocatalytic activity was achieved with BiOCl{sub 0.3}/BiOBr{sub 0.3}/BiOI{sub 0.4} fibers under solar light irradiation. X-ray photoelectron spectroscopy (XPS) peaks due to C−O and C=O were observed at 286.0 and 288.3 eV, respectively, it indicated that the BiOCl{sub x}/BiOBr{sub y}/BiOI{sub z} mixture had been successfully doped on the polyacrylonitrile (PAN) fibers. Furthermore, X-ray diffraction (XRD) results also confirmed that we had synthesized the as-prepared composite nanofibers successfully. Photocatalytic activities of BiOCl{sub 0.3}/BiOBr{sub 0.3}/BiOI{sub 0.4} were up to 3 times higher than the pure BiOCl, BiOBr and BiOI samples, respectively.

Polyacrylonitrile nanofiber as polar solvent N,N-dimethyl formamide sensor based on quartz crystal microbalance technique

Science.gov (United States)

Rianjanu, A.; Julian, T.; Hidayat, S. N.; Suyono, E. A.; Kusumaatmaja, A.; Triyana, K.

2018-04-01

Here, we describe an N,N-dimethyl formamide (DMF) vapour sensor fabricated by coating polyacrylonitrile (PAN) nanofiber structured on quartz crystal microbalance (QCM). The PAN nanofiber sensors with an average diameter of 225 nm to 310 nm were fabricated via electrospinning process with different mass deposition on QCM substrate. The nanostructured of PAN nanofiber offers a high specific surface area that improved the sensing performance of nanofiber sensors. Benefiting from that fine structure, and high polymer-solvent affinity between PAN and DMF, the development of DMF sensors presented good response at ambient temperature. Since there is no chemical reaction between PAN nanofiber and DMF vapour, weak physical interaction such absorption and swelling were responsible for the sensing behavior. The results are indicating that the response of PAN nanofiber sensors has more dependency on the nanofiber structure (specific surface area) rather than its mass deposition. The sensor also showed good stability after a few days sensing. These findings have significant implications for developing DMF vapour sensor based on QCM coated polymer nanofibers.

Lecithin blended polyamide-6 high aspect ratio nanofiber scaffolds via electrospinning for human osteoblast cell culture

Energy Technology Data Exchange (ETDEWEB)

Nirmala, R. [Bio-nano System Engineering, College of Engineering, Chonbuk National University, Jeonju, 561 756 (Korea, Republic of); Park, Hye-Min [Department of Pharmacology and Toxicology, College of Veterinary Medicine, Chonbuk National University, Jeonju 561 756 (Korea, Republic of); Navamathavan, R. [School of Advanced Materials Engineering, Chonbuk National University, Jeonju 561 756 (Korea, Republic of); Kang, Hyung-Sub [Department of Pharmacology and Toxicology, College of Veterinary Medicine, Chonbuk National University, Jeonju 561 756 (Korea, Republic of); El-Newehy, Mohamed H. [Petrochemical Research Chair, Department of Chemistry, College of Science, King Saud University, Riyadh 11451 (Saudi Arabia); Kim, Hak Yong, E-mail: khy@jbnu.ac.kr [Petrochemical Research Chair, Department of Chemistry, College of Science, King Saud University, Riyadh 11451 (Saudi Arabia); Center for Healthcare Technology and Development, Chonbuk National University, Jeonju, 561 756 (Korea, Republic of)

2011-03-12

In this study, we focused on the preparation and characterization of lecithin blended polyamide-6 nanofibers via an electrospinning process for human osteoblastic (HOB) cell culture applications. The morphological, structural characterizations and thermal properties of polyamide-6/lecithin nanofibers were determined by using scanning electron microscopy (SEM), field-emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, differential scanning calorimetry (DSC) and thermogravimetry (TGA). SEM images revealed that the nanofibers were well-oriented with good incorporation of lecithin. FT-IR results indicated the presence of amino groups of lecithin in the blended nanofibers. TGA analysis revealed that the onset degradation temperature decreased with increasing lecithin content in the blended nanofibers. The morphological features of cells attached on polyamide-6/lecithin nanofibers were confirmed by SEM. The adhesion, viability and proliferation properties of osteoblast cells on the polyamide-6/lecithin blended nanofibers were analyzed by in vitro cell compatibility test. This study demonstrated the non-cytotoxic behavior of electrospun polyamide-6/lecithin nanofibers for the osteoblast cell culture.

Lecithin blended polyamide-6 high aspect ratio nanofiber scaffolds via electrospinning for human osteoblast cell culture

International Nuclear Information System (INIS)

Nirmala, R.; Park, Hye-Min; Navamathavan, R.; Kang, Hyung-Sub; El-Newehy, Mohamed H.; Kim, Hak Yong

2011-01-01

In this study, we focused on the preparation and characterization of lecithin blended polyamide-6 nanofibers via an electrospinning process for human osteoblastic (HOB) cell culture applications. The morphological, structural characterizations and thermal properties of polyamide-6/lecithin nanofibers were determined by using scanning electron microscopy (SEM), field-emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, differential scanning calorimetry (DSC) and thermogravimetry (TGA). SEM images revealed that the nanofibers were well-oriented with good incorporation of lecithin. FT-IR results indicated the presence of amino groups of lecithin in the blended nanofibers. TGA analysis revealed that the onset degradation temperature decreased with increasing lecithin content in the blended nanofibers. The morphological features of cells attached on polyamide-6/lecithin nanofibers were confirmed by SEM. The adhesion, viability and proliferation properties of osteoblast cells on the polyamide-6/lecithin blended nanofibers were analyzed by in vitro cell compatibility test. This study demonstrated the non-cytotoxic behavior of electrospun polyamide-6/lecithin nanofibers for the osteoblast cell culture.

Mechanical properties and cellular response of novel electrospun nanofibers for ligament tissue engineering: Effects of orientation and geometry.

Science.gov (United States)

Pauly, Hannah M; Kelly, Daniel J; Popat, Ketul C; Trujillo, Nathan A; Dunne, Nicholas J; McCarthy, Helen O; Haut Donahue, Tammy L

2016-08-01

Electrospun nanofibers are a promising material for ligamentous tissue engineering, however weak mechanical properties of fibers to date have limited their clinical usage. The goal of this work was to modify electrospun nanofibers to create a robust structure that mimics the complex hierarchy of native tendons and ligaments. The scaffolds that were fabricated in this study consisted of either random or aligned nanofibers in flat sheets or rolled nanofiber bundles that mimic the size scale of fascicle units in primarily tensile load bearing soft musculoskeletal tissues. Altering nanofiber orientation and geometry significantly affected mechanical properties; most notably aligned nanofiber sheets had the greatest modulus; 125% higher than that of random nanofiber sheets; and 45% higher than aligned nanofiber bundles. Modifying aligned nanofiber sheets to form aligned nanofiber bundles also resulted in approximately 107% higher yield stresses and 140% higher yield strains. The mechanical properties of aligned nanofiber bundles were in the range of the mechanical properties of the native ACL: modulus=158±32MPa, yield stress=57±23MPa and yield strain=0.38±0.08. Adipose derived stem cells cultured on all surfaces remained viable and proliferated extensively over a 7 day culture period and cells elongated on nanofiber bundles. The results of the study suggest that aligned nanofiber bundles may be useful for ligament and tendon tissue engineering based on their mechanical properties and ability to support cell adhesion, proliferation, and elongation. Copyright © 2016 Elsevier Ltd. All rights reserved.

Morphological Characterization of Nanofibers: Methods and Application in Practice

Directory of Open Access Journals (Sweden)

Jakub Širc

2012-01-01

Full Text Available Biomedical applications such as wound dressing for skin regeneration, stem cell transplantation, or drug delivery require special demands on the three-dimensional porous scaffolds. Besides the biocompatibility and mechanical properties, the morphology is the most important attribute of the scaffold. Specific surface area, volume, and size of the pores have considerable effect on cell adhesion, growth, and proliferation. In the case of incorporated biologically active substances, their release is also influenced by the internal structure of nanofibers. Although many scientific papers are focused on the preparation of nanofibers and evaluation of biological tests, the morphological characterization was described just briefly as service methods. The aim of this paper is to summarize the methods applicable for morphological characterization of nanofibers and supplement it by the results of our research. Needleless electrospinning technique was used to prepare nanofibers from polylactide, poly(ε-caprolactone, gelatin, and polyamide. Scanning electron microscopy was used to evaluate the fiber diameters and to reveal eventual artifacts in the nanofibrous structure. Nitrogen adsorption/desorption measurements were employed to measure the specific surface areas. Mercury porosimetry was used to determine total porosities and compare pore size distributions of the prepared samples.

Surface modification of polyvinyl alcohol/malonic acid nanofibers by gaseous dielectric barrier discharge plasma for glucose oxidase immobilization

Science.gov (United States)

Afshari, Esmail; Mazinani, Saeedeh; Ranaei-Siadat, Seyed-Omid; Ghomi, Hamid

2016-11-01

Polymeric nanofiber prepares a suitable situation for enzyme immobilization for variety of applications. In this research, we have fabricated polyvinyl alcohol (PVA)/malonic acid nanofibers using electrospinning. After fabrication of nanofibers, the effect of air, nitrogen, CO2, and argon DBD (dielectric barrier discharge) plasmas on PVA/malonic acid nanofibers were analysed. Among them, air plasma had the most significant effect on glucose oxidase (GOx) immobilization. Attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectrum analysis and X-ray photoelectron spectroscopy (XPS) results revealed that in case of air plasma modified nanofibers, the carboxyl groups on the surface are increased. The scanning electron microscopy (SEM) images showed that, after GOx immobilization, the modified nanofibers with plasma has retained its nanofiber structure. Finally, we analysed reusability and storage stability of GOx immobilized on plasma modified and unmodified nanofibers. The results were more satisfactory for modified nanofibers with respect to unmodified ones.

Investigation of electrochemical actuation by polyaniline nanofibers

Science.gov (United States)

Mehraeen, Shayan; Alkan Gürsel, Selmiye; Papila, Melih; Çakmak Cebeci, Fevzi

2017-09-01

Polyaniline nanofibers have shown promising electrical and electrochemical properties which make them prominent candidates in the development of smart systems employing sensors and actuators. Their electrochemical actuation potential is demonstrated in this study. A trilayer composite actuator based on polyaniline nanofibers was designed and fabricated. Cross-linked polyvinyl alcohol was sandwiched between two polyaniline nanofibrous electrodes as ion-containing electrolyte gel. First, electrochemical behavior of a single electrode was studied, showing reversible redox peak pairs in 1 M HCl using a cyclic voltammetry technique. High aspect ratio polyaniline nanofibers create a porous network which facilitates ion diffusion and thus accelerates redox reactions. Bending displacement of the prepared trilayer actuator was then tested and reported under an AC potential stimulation as low as 0.5 V in a variety of frequencies from 50 to 1000 mHz, both inside 1 M HCl solution and in air. Decay of performance of the composite actuator in air is investigated and it is reported that tip displacement in a solution was stable and repeatable for 1000 s in all selected frequencies.

Laser-induced charge separation in organic nanofibers

DEFF Research Database (Denmark)

Tavares, Luciana; Behn, Dino; Kjelstrup-Hansen, Jakob

Organic semiconductors have unique properties that can be tailored via synthetic chemistry for specific applications, which combined with their low price and straight-forward processing over large areas make them interesting materials for future devices. Certain oligomers can self-assemble into c......Organic semiconductors have unique properties that can be tailored via synthetic chemistry for specific applications, which combined with their low price and straight-forward processing over large areas make them interesting materials for future devices. Certain oligomers can self......-assemble into crystalline nanofibers by vapor deposition onto muscovite mica substrates, and we have recently shown that such nanofibers can be transferred to different substrates by roll-printing and used as the active material in e.g. organic field-effect transistors (OFETs), organic light-emitting transistors (OLETs......), and organic phototransistors (OPTs). However, several device-related issues incl. charge-separation and local band structure remain poorly understood. In this work, we use electrostatic force microscopy (EFM) combined with optical microscopy to study the local surface charge of an individual organic nanofiber...

Analysis of the magnetic properties in hard-magnetic nanofibers composite

Science.gov (United States)

Murillo-Ortíz, R.; Mirabal-García, M.; Martínez-Huerta, J. M.; Cabal Velarde, J. G.; Castaneda-Robles, I. E.; Lobo-Guerrero, A.

2018-03-01

The magnetic properties of the strontium hexaferrite nanoparticles were studied as they were embedded at different concentrations in poly(vinyl alcohol) (PVA) nanofibers. These nanoparticles were prepared using the Pechini method and a low frequency sonication process obtaining a 3.4 nm average diameter. The composite consisting of hard magnetic nanoparticles homogeneously dispersed in a polymeric matrix was fabricated using a homemade electrospinning with 25 kV DC power supply. The obtained nanofibers had an average diameter of 110 nm, and nanoparticles were arranged and distributed within the nanofibers under the influence of a strong electric field. The configuration of the magnetic nanoparticles in the PVA nanofibers was such that the interparticle exchange interaction became negligible, while the magnetostatic interaction turned out predominant. The results reveal a considerable improvement in the energy product (BHmax) and in the squareness ratio (Mr/Ms) for nanoparticle concentrations between 15 and 30% per gram of PVA. The nanoparticles arrangement occurred at densities below the percolation concentration enhanced the hard-magnetic properties of the nanofibers, which indicates that the organization of the particles along the fibers induces anisotropy from the magnetostatic interaction among the magnetic nanoparticles. Finally, we close the discussion analyzing the observed effect below the percolation threshold, where the induced anisotropy caused the reduction of the full-width at half-maximum of the switching field distribution curves.

High electrochemical energy storage in self-assembled nest-like CoO nanofibers with long cycle life

Energy Technology Data Exchange (ETDEWEB)

Pramanik, Atin; Maiti, Sandipan [CSIR-Central Glass & Ceramic Research Institute, Fuel Cell & Battery Division (India); Sreemany, Monjoy [CSIR-Central Glass & Ceramic Research Institute, Advanced Mechanical and Materials Characterization Division (India); Mahanty, Sourindra, E-mail: mahanty@cgcri.res.in [CSIR-Central Glass & Ceramic Research Institute, Fuel Cell & Battery Division (India)

2016-04-15

Developing efficient electrode material is essential to keep pace with the demand for high energy density together with high power density and long cycle life in next generation energy storage devices. Herein, we report the electrochemical properties of hydrothermally synthesized CoO nanofibers of diameter 30–80 nm assembled in a nest-like morphology which showed a very high reversible lithium storage capacity of 2000 mA h g{sup −1} after 600 cycles at 0.1 mA cm{sup −2} as lithium-ion battery anode. Systematic investigation by ex situ transmission electron microscopy, X-ray photoelectron spectroscopy, cyclic voltammetry, and impedance spectroscopy at different cycling stages indicated that the extraordinary performance could be related to an enhancement in the Co{sup 2+}↔Co{sup x+} (2 < x ≤ 3) redox process in addition to the commonly believed structural and morphological evolution during cycling favoring generation of large number of accessible active sites for lithium insertion. Further, when examined as a supercapacitor electrode in 1.0 M KOH, a capacitance of 1167 F g{sup −1} is achieved from these 1D CoO nanofibers after 10,000 charge discharge cycles at a high current density of 5 A g{sup −1} demonstrating good application potential.Graphical AbstractNest-like CoO nanofibers showed a reversible lithium storage capacity of 2000 mA h g{sup −1} after 600 cycles as LIB anode and a capacitance of 1167 F g{sup −1} after 10,000 cycles as electrochemical supercapacitor.

Photocatalysis of sub-ppm limonene over multiwalled carbon nanotubes/titania composite nanofiber under visible-light irradiation

International Nuclear Information System (INIS)

Jo, Wan-Kuen; Kang, Hyun-Jung

2015-01-01

Highlights: • A multiwalled carbon nanotube/titania composite nanofiber (MTCN) was synthesized. • Photocatalytic function of visible-activated MTCN was examined using tubular reactor. • MTCNs could be effectively used for the purification of sub-ppm gas-phase limonene. • The experimental results agreed well with Langmuir–Hinshelwood model. • Certain gas-phase intermediates were determined, but not for adsorbed intermediates. - Abstract: This study was conducted under visible-light exposure to investigate the photocatalytic characteristics of a multiwalled carbon nanotube/titania (TiO 2 ) composite nanofiber (MTCN) using a continuous-flow tubular reactor. The MTCN was prepared by a sol–gel process, followed by an electrospinning technique. The photocatalytic decomposition efficiency for limonene on the MTCN was higher than those obtained from reference TiO 2 nanofibers or P25 TiO 2 , and the experimental results agreed well with the Langmuir–Hinshelwood model. The CO concentrations generated during the photocatalysis did not reach levels toxic to humans. The mineralization efficiency for limonene on the MTCN was also higher than that for P25 TiO 2 . Moreover, the mineralization efficiency obtained using the MTCN increased steeply from 8.3 to 91.1% as the residence time increased from 7.8 to 78.0 s, compared to the increase in the decomposition efficiencies for limonene from 90.1 to 99.9%. Three gas-phase intermediates (methacrolein, acetic acid, and limonene oxide) were quantitatively determined for the photocatalysis for limonene over the MTCN, whereas only two intermediates (acetic acid and limonene oxide) were quantitatively determined over P25 TiO 2 . Other provisional gas-phase intermediates included cyclopropyl methyl ketone and 2-ethylbutanal

Photocatalysis of sub-ppm limonene over multiwalled carbon nanotubes/titania composite nanofiber under visible-light irradiation

Energy Technology Data Exchange (ETDEWEB)

Jo, Wan-Kuen, E-mail: wkjo@knu.ac.kr; Kang, Hyun-Jung

2015-02-11

Highlights: • A multiwalled carbon nanotube/titania composite nanofiber (MTCN) was synthesized. • Photocatalytic function of visible-activated MTCN was examined using tubular reactor. • MTCNs could be effectively used for the purification of sub-ppm gas-phase limonene. • The experimental results agreed well with Langmuir–Hinshelwood model. • Certain gas-phase intermediates were determined, but not for adsorbed intermediates. - Abstract: This study was conducted under visible-light exposure to investigate the photocatalytic characteristics of a multiwalled carbon nanotube/titania (TiO{sub 2}) composite nanofiber (MTCN) using a continuous-flow tubular reactor. The MTCN was prepared by a sol–gel process, followed by an electrospinning technique. The photocatalytic decomposition efficiency for limonene on the MTCN was higher than those obtained from reference TiO{sub 2} nanofibers or P25 TiO{sub 2}, and the experimental results agreed well with the Langmuir–Hinshelwood model. The CO concentrations generated during the photocatalysis did not reach levels toxic to humans. The mineralization efficiency for limonene on the MTCN was also higher than that for P25 TiO{sub 2}. Moreover, the mineralization efficiency obtained using the MTCN increased steeply from 8.3 to 91.1% as the residence time increased from 7.8 to 78.0 s, compared to the increase in the decomposition efficiencies for limonene from 90.1 to 99.9%. Three gas-phase intermediates (methacrolein, acetic acid, and limonene oxide) were quantitatively determined for the photocatalysis for limonene over the MTCN, whereas only two intermediates (acetic acid and limonene oxide) were quantitatively determined over P25 TiO{sub 2}. Other provisional gas-phase intermediates included cyclopropyl methyl ketone and 2-ethylbutanal.

Polyacrylonitrile nanofibers coated with silver nanoparticles using a modified coaxial electrospinning process

Directory of Open Access Journals (Sweden)

Yu DG

2012-11-01

Full Text Available Deng-Guang Yu,1 Jie Zhou,2 Nicholas P Chatterton,3 Ying Li,1 Jing Huang,2 Xia Wang11School of Materials Science and Engineering, University of Shanghai for Science and Technology, Shanghai, People's Republic of China; 2School of Life Sciences, East China Normal University, Shanghai, People's Republic of China; 3Faculty of Life Sciences, London Metropolitan University, London, United KingdomBackground: The objective of this investigation was to develop a new class of antibacterial material in the form of nanofibers coated with silver nanoparticles (AgNPs using a modified coaxial electrospinning approach. Through manipulation of the distribution on the surface of nanofibers, the antibacterial effect of Ag can be improved substantially.Methods: Using polyacrylonitrile (PAN as the filament-forming polymer matrix, an electrospinnable PAN solution was prepared as the core fluid. A silver nitrate (AgNO3 solution was exploited as sheath fluid to carry out the modified coaxial electrospinning process under varied sheath-to-core flow rate ratios.Results: Scanning electron microscopy and transmission electron microscopy demonstrated that the sheath AgNO3 solution can take a role in reducing the nanofibers' diameters significantly, a sheath-to-core flow rate ratio of 0.1 and 0.2 resulting in PAN nanofibers with diameters of 380 ± 110 nm and 230 ± 70 nm respectively. AgNPs are well distributed on the surface of PAN nanofibers. The antibacterial experiments demonstrated that these nanofibers show strong antimicrobial activities against Bacillus subtilis Wb800, and Escherichia coli dh5α.Conclusion: Coaxial electrospinning with AgNO3 solution as sheath fluid not only facilitates the electrospinning process, providing nanofibers with reduced diameters, but also allows functionalization of the nanofibers through coating with functional ingredients, effectively ensuring that the active antibacterial component is on the surface of the material, which leads to

Mirror-finished superhydrophobic aluminum surfaces modified by anodic alumina nanofibers and self-assembled monolayers

Science.gov (United States)

Nakajima, Daiki; Kikuchi, Tatsuya; Natsui, Shungo; Suzuki, Ryosuke O.

2018-05-01

We demonstrate mirror-finished superhydrophobic aluminum surfaces fabricated via the formation of anodic alumina nanofibers and subsequent modification with self-assembled monolayers (SAMs). High-density anodic alumina nanofibers were formed on the aluminum surface via anodizing in a pyrophosphoric acid solution. The alumina nanofibers became tangled and bundled by further anodizing at low temperature because of their own weight, and the aluminum surface was completely covered by the long falling nanofibers. The nanofiber-covered aluminum surface exhibited superhydrophilic behavior, with a contact angle measuring less than 10°. As the nanofiber-covered aluminum surface was modified with n-alkylphosphonic acid SAMs, the water contact angle drastically shifted to superhydrophobicity, measuring more than 150°. The contact angle increased with the applied voltage during pyrophosphoric acid anodizing, the anodizing time, and the number of carbon atoms contained in the SAM molecules modified on the alumina nanofibers. By optimizing the anodizing and SAM-modification conditions, superhydrophobic behavior could be achieved with only a brief pyrophosphoric acid anodizing period of 3 min and subsequent simple immersion in SAM solutions. The superhydrophobic aluminum surface exhibited a high reflectance, measuring approximately 99% across most of the visible spectrum, similar to that of an electropolished aluminum surface. Therefore, our mirror-finished superhydrophobic aluminum surface based on anodic alumina nanofibers and SAMs can be used as a reflective mirror in various optical applications such as concentrated solar power systems.

Size-dependent mechanical properties of PVA nanofibers reduced via air plasma treatment

International Nuclear Information System (INIS)

Fu Qiang; Song Xuefeng; Gao Jingyun; Han Xiaobing; Zhao Qing; Yu Dapeng; Jin Yu; Jiang Xingyu

2010-01-01

Organic nanowires/fibers have great potential in applications such as organic electronics and soft electronic techniques. Therefore investigation of their mechanical performance is of importance. The Young's modulus of poly(vinyl alcohol) (PVA) nanofibers was analyzed by scanning probe microscopy (SPM) methods. Air plasma treatment was used to reduce the nanofibers to different sizes. Size-dependent mechanical properties of PVA nanofibers were studied and revealed that the Young's modulus increased dramatically when the scales became very small (<80 nm).

Size-dependent mechanical properties of PVA nanofibers reduced via air plasma treatment.

Science.gov (United States)

Fu, Qiang; Jin, Yu; Song, Xuefeng; Gao, Jingyun; Han, Xiaobing; Jiang, Xingyu; Zhao, Qing; Yu, Dapeng

2010-03-05

Organic nanowires/fibers have great potential in applications such as organic electronics and soft electronic techniques. Therefore investigation of their mechanical performance is of importance. The Young's modulus of poly(vinyl alcohol) (PVA) nanofibers was analyzed by scanning probe microscopy (SPM) methods. Air plasma treatment was used to reduce the nanofibers to different sizes. Size-dependent mechanical properties of PVA nanofibers were studied and revealed that the Young's modulus increased dramatically when the scales became very small (<80 nm).

A co-confined carbonization approach to aligned nitrogen-doped mesoporous carbon nanofibers and its application as an adsorbent

Energy Technology Data Exchange (ETDEWEB)

Chen, Aibing [College of Chemical and Pharmaceutical Engineering, Hebei University of Science and Technology, Shijiazhuang 050018 (China); Liu, Chao [College of Gemmology and Material Technics, Shijiazhuang University of Economic, Huaian Road 136, Shijiazhuang 050031 (China); Yu, Yifeng; Hu, Yongqi; Lv, Haijun; Zhang, Yue; Shen, Shufeng [College of Chemical and Pharmaceutical Engineering, Hebei University of Science and Technology, Shijiazhuang 050018 (China); Zhang, Jian [Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo 315201 (China)

2014-07-15

Highlights: • MCNFs were synthesized by a co-confined carbonization method. • The diameter size of MCNFs with bimodal mesoporous structure can be modulated. • The obtained MCNFs manifest better adsorption capacity for SO{sub 2}, CO{sub 2} and Cd{sup 2+}. - Abstract: Nitrogen-doped carbon nanofibers (MCNFs) with an aligned mesoporous structure were synthesized by a co-confined carbonization method using anodic aluminum oxide (AAO) membrane and tetraethylorthosilicate (TEOS) as co-confined templates and ionic liquids as the precursor. The as-synthesized MCNFs with the diameter of 80–120 nm possessed a bulk nitrogen content of 5.3 wt% and bimodal mesoporous structure. The nitrogen atoms were mostly bound to the graphitic network in two forms, i.e. pyridinic and pyrrolic nitrogen, providing adsorption sites for acidic gases like SO{sub 2} and CO{sub 2}. Cyclic experiments revealed a considerable stability of MCNFs over 20 runs of SO{sub 2} adsorption and 15 runs for CO{sub 2} adsorption. The MCNFs also have a preferable adsorption performance for Cd{sup 2+}.

Recent Advances in Cell Electrospining of Natural and Synthetic Nanofibers for Regenerative Medicine.

Science.gov (United States)

Zamani, Reza; Aval, Sedigheh Fekri; Pilehvar-Soltanahmadi, Younes; Nejati-Koshki, Kazem; Zarghami, Nosratollah

2018-01-22

The progression of nanotechnology provides opportunities to manipulate synthetic and natural materials to mimic the natural structure for tissue engineering applications. The electrospinning technique applies electrostatic principle to fabricate electrospun nanofibers. Nanofiber scaffolds are precisely similar to the native extracellular matrix (ECM) and support cell proliferation, adhesion, tendency to preserve their phenotypic shape and directed growth according to the nanofiber direction. This study reviewed both the natural and synthetic type of nanofibers and described the different properties used to trigger certain process in the tissue development. Also, the potential applications of electrospun scaffolds for regenerative medicine were summarized. © Georg Thieme Verlag KG Stuttgart · New York.

Mechanical properties of organic nanofibers

DEFF Research Database (Denmark)

Kjelstrup-Hansen, Jakob; Hansen, Ole; Rubahn, H.R.

2006-01-01

Intrinsic elastic and inelastic mechanical Properties of individual, self-assembled, quasi-single-crystalline para-hexaphenylene nanofibers supported on substrates with different hydrophobicities are investigated as well as the interplay between the fibers and the underlying substrates. We find...

The use of chitosan/PLA nano-fibers by emulsion eletrospinning for periodontal tissue engineering.

Science.gov (United States)

Shen, Renze; Xu, Weihong; Xue, Yanxiang; Chen, Luyuan; Ye, Haicheng; Zhong, Enyi; Ye, Zhanchao; Gao, Jie; Yan, Yurong

2018-04-16

In this study, nanofibrous scaffolds base on pure polylactic acid (PLA) and chitosan/PLA blends were fabricated by emulsion eletrospinning. By modulating their mechanical and biological properties, cell-compatible and biodegradable scaffolds were developed for periodontal bone regeneration. Pure PLA and different weight ratios of chitosan nano-particle/PLA nano-fibers were fabricated by emulsion eletrospinning. Scanning electron microscope (SEM) was performed to observe the morphology of nano-fibers. Mechanical properties of nano-fibers were tested by single fiber strength tester. Hydrophilic/hydrophobic nature of the nano-fibers was observed by stereomicroscope. In vitro degradation was also tested. Cells were seeded on nano-fibers scaffolds. Changes in cell adhesion, proliferation and osteogenic differentiation were tested by MTT assay and Alizarin Red S staining. Reverse transcription-polymerase chain reaction (RT-PCR) assay was used to evaluate the expression of (Toll-like receptor 4) TLR4, IL-6, IL-8, IL-1β, OPG, RUNX2 mRNA. It is shown that the mean diameter of nano-fibers is about 200 nm. The mean diameter of chitosan nano-particles is about 50 nm. The combination of chitosan nano-particles enhanced the mechanical properties of pure PLA nano-fibers. By adding a certain amount of chitosan nano-particles, it promoted cell adhesion. It also promoted the osteogenic differentiation of bone marrow stem cells (BMSCs) by elevating the expression of osteogenic marker genes such as BSP, Ocn, collagen I, and OPN and enhanced ECM mineralization. Nonetheless, it caused higher expression of inflammatory mediators and TLR4 of human periodontal ligament cells (hPDLCs). The combination of chitosan nano-particles enhanced the mechanical properties of pure PLA nano-fibers and increased its hydrophilicity. Pure PLA nano-fibers scaffold facilitated BMSCs proliferation. Adding an appropriate amount of chitosan nano-particles may promote its properties of cell proliferation

Pore-Structure-Optimized CNT-Carbon Nanofibers from Starch for Rechargeable Lithium Batteries

Directory of Open Access Journals (Sweden)

Yongjin Jeong

2016-12-01

Full Text Available Porous carbon materials are used for many electrochemical applications due to their outstanding properties. However, research on controlling the pore structure and analyzing the carbon structures is still necessary to achieve enhanced electrochemical properties. In this study, mesoporous carbon nanotube (CNT-carbon nanofiber electrodes were developed by heat-treatment of electrospun starch with carbon nanotubes, and then applied as a binder-free electrochemical electrode for a lithium-ion battery. Using the unique lamellar structure of starch, mesoporous CNT-carbon nanofibers were prepared and their pore structures were controlled by manipulating the heat-treatment conditions. The activation process greatly increased the volume of micropores and mesopores of carbon nanofibers by etching carbons with CO2 gas, and the Brunauer-Emmett-Teller (BET specific area increased to about 982.4 m2·g−1. The activated CNT-carbon nanofibers exhibited a high specific capacity (743 mAh·g−1 and good cycle performance (510 mAh·g−1 after 30 cycles due to their larger specific surface area. This condition presents many adsorption sites of lithium ions, and higher electrical conductivity, compared with carbon nanofibers without CNT. The research suggests that by controlling the heat-treatment conditions and activation process, the pore structure of the carbon nanofibers made from starch could be tuned to provide the conditions needed for various applications.

La0.6Sr0.4Co0.2Fe0.8O3-δ nanofiber cathode for intermediate-temperature solid oxide fuel cells by water-based sol-gel electrospinning: Synthesis and electrochemical behaviour

DEFF Research Database (Denmark)

Enrico, Anna; Zhang, Wenjing (Angela); Traulsen, Marie Lund

2018-01-01

Water-based sol-gel electrospinning is employed to manufacture perovskite oxide La0.6Sr0.4Co0.2Fe0.8O3-δ (LSCF) nanofiber cathodes for intermediate-temperature solid oxide fuel cells. LSCF fibrous scaffolds are synthesized through electrospinning of a sol-gel solution employing water as the only...

The fabrication and testing of electrospun silica nanofiber membranes for the detection of proteins

International Nuclear Information System (INIS)

Tsou, P-H; Kameoka, J; Chou, C-K; Saldana, S M; Hung, M-C

2008-01-01

In this study, we fabricated electrospun silica nanofiber membranes and investigated their use in biomolecular sensing. The diameter, porosity and surface-to-volume ratio of nanofiber membranes were investigated under different fabrication conditions. Using this type of nanofiber membrane, enzyme-linked immunosorbent assay (ELISA) was performed, and the results were compared with those obtained with conventional ELISA using polystyrene well plates. The minimum detectable concentration was determined as 0.19 ng ml -1 (1.6 pM), which is 32 times lower than that of conventional ELISA. In addition, the detection time for all processes for the nanofiber membrane was reduced to 1 h, compared with 1 day for conventional ELISA. The increased sensitivity, faster reaction time, and affordability of the nanofiber membrane make it well suited for bio-chip use.

Electrospun tilapia collagen nanofibers accelerating wound healing via inducing keratinocytes proliferation and differentiation.

Science.gov (United States)

Zhou, Tian; Wang, Nanping; Xue, Yang; Ding, Tingting; Liu, Xin; Mo, Xiumei; Sun, Jiao

2016-07-01

The development of biomaterials with the ability to induce skin wound healing is a great challenge in biomedicine. In this study, tilapia skin collagen sponge and electrospun nanofibers were developed for wound dressing. The collagen sponge was composed of at least two α-peptides. It did not change the number of spleen-derived lymphocytes in BALB/c mice, the ratio of CD4(+)/CD8(+) lymphocytes, and the level of IgG or IgM in Sprague-Dawley rats. The tensile strength and contact angle of collagen nanofibers were 6.72±0.44MPa and 26.71±4.88°, respectively. They also had good thermal stability and swelling property. Furthermore, the nanofibers could significantly promote the proliferation of human keratinocytes (HaCaTs) and stimulate epidermal differentiation through the up-regulated gene expression of involucrin, filaggrin, and type I transglutaminase in HaCaTs. The collagen nanofibers could also facilitate rat skin regeneration. In the present study, electrospun biomimetic tilapia skin collagen nanofibers were succesfully prepared, were proved to have good bioactivity and could accelerate rat wound healing rapidly and effectively. These biological effects might be attributed to the biomimic extracellular matrix structure and the multiple amino acids of the collagen nanofibers. Therefore, the cost-efficient tilapia collagen nanofibers could be used as novel wound dressing, meanwhile effectively avoiding the risk of transmitting animal disease in the future clinical apllication. Copyright © 2016 Elsevier B.V. All rights reserved.

Modeling temperature dependent singlet exciton dynamics in multilayered organic nanofibers

Science.gov (United States)

de Sousa, Leonardo Evaristo; de Oliveira Neto, Pedro Henrique; Kjelstrup-Hansen, Jakob; da Silva Filho, Demétrio Antônio

2018-05-01

Organic nanofibers have shown potential for application in optoelectronic devices because of the tunability of their optical properties. These properties are influenced by the electronic structure of the molecules that compose the nanofibers and also by the behavior of the excitons generated in the material. Exciton diffusion by means of Förster resonance energy transfer is responsible, for instance, for the change with temperature of colors in the light emitted by systems composed of different types of nanofibers. To study in detail this mechanism, we model temperature dependent singlet exciton dynamics in multilayered organic nanofibers. By simulating absorption and emission spectra, the possible Förster transitions are identified. Then, a kinetic Monte Carlo model is employed in combination with a genetic algorithm to theoretically reproduce time-resolved photoluminescence measurements for several temperatures. This procedure allows for the obtainment of different information regarding exciton diffusion in such a system, including temperature effects on the Förster transfer efficiency and the activation energy of the Förster mechanism. The method is general and may be employed for different systems where exciton diffusion plays a role.

Tyrosinase-Mediated Construction of a Silk Fibroin/Elastin Nanofiber Bioscaffold.

Science.gov (United States)

Hong, Yanqing; Zhu, Xueke; Wang, Ping; Fu, Haitian; Deng, Chao; Cui, Li; Wang, Qiang; Fan, Xuerong

2016-04-01

Elastin has characteristics of elasticity, biological activity, and mechanical stability. In the present work, tyrosinase-mediated construction of a bioscaffold with silk fibroin and elastin was carried out, aiming at developing a novel medical biomaterial. The efficiency of enzymatic oxidation of silk fibroin and the covalent reaction between fibroin and elastin were examined by spectrophotometry, sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE), and size exclusion chromatography (SEC). The properties of composite air-dried and nanofiber scaffolds were investigated. The results reveal that elastin was successfully bonded to silk fibroins, resulting in an increase in molecular weight of fibroin proteins. ATR-FTIR spectra indicated that tyrosinase treatment impacted the conformational structure of fibroin-based membrane. The thermal behaviors and mechanical properties of the tyrosinase-treated scaffolds were also improved compared with the untreated group. NIH/3T3 cells exhibited optimum densities when grown on the nanofiber scaffold, implying that the nanofiber scaffold has enhanced biocompatibility compared to the air-dried scaffold. A biological nanofiber scaffold constructed from tyrosinase-treated fibroin and elastin could potentially be utilized in biomedical applications.

Sub-nanomolar sensing of ionic mercury with polymeric electrospun nanofibers

Energy Technology Data Exchange (ETDEWEB)

Kacmaz, Sibel [University of Dokuz Eylul, The Graduate School of Natural and Applied Sciences, Department of Chemistry, 35160 Izmir (Turkey); Ertekin, Kadriye, E-mail: kadriye.ertekin@deu.edu.tr [University of Dokuz Eylul, Faculty of Sciences, Department of Chemistry, 35160 Izmir (Turkey); University of Dokuz Eylul, Center for Fabrication and Application of Electronic Materials (EMUM), 35160 Izmir (Turkey); Suslu, Aslihan [University of Dokuz Eylul, The Graduate School of Natural and Applied Sciences, Department of Chemistry, 35160 Izmir (Turkey); University of Dokuz Eylul, Faculty Engineering, Department of Metallurgical and Materials Engineering, 35160 Izmir (Turkey); Ergun, Yavuz [University of Dokuz Eylul, Faculty of Sciences, Department of Chemistry, 35160 Izmir (Turkey); Celik, Erdal [University of Dokuz Eylul, Center for Fabrication and Application of Electronic Materials (EMUM), 35160 Izmir (Turkey); University of Dokuz Eylul, Faculty Engineering, Department of Metallurgical and Materials Engineering, 35160 Izmir (Turkey); Cocen, Umit [University of Dokuz Eylul, Faculty Engineering, Department of Metallurgical and Materials Engineering, 35160 Izmir (Turkey)

2012-03-15

Ethyl cellulose (EC) based electrospun nanofibers were exploited for sub-nanomolar level optical chemical sensing of ionic mercury. An azomethine ionophore was used as Hg (I) and Hg (II) sensing material. Ethyl cellulose nanofibers with varying amounts of the ionic liquid; 1-ethyl-3-methylimidazolium tetrafluoroborate (EMIMBF{sub 4}) were prepared and characterized. The nanofibers were fabricated by electrospinning technique. The offered chemosensor allow determination of mercury ions in a large linear working range between 1.0 Multiplication-Sign 10{sup -10} and 1.0 Multiplication-Sign 10{sup -4} mol L{sup -1}. Limit of detection was found to be 0.07 nM which makes this technique alternative to cold-vapor atomic absorption spectrometry (CV-AAS), flame emission methods and to inductively coupled plasma-mass spectrometry (ICP-MS). The electrospun nanofibers exhibited excellent sensitivity for Hg (II) with respect to the continuous thin films prepared with same composition. The observed high sensitivity can be attributed to the high surface area of the nanofibrous materials and enhanced diffusibility of the mercury ions to the ionophore.

Vorinostat-eluting poly(DL-lactide-co-glycolide nanofiber-coated stent for inhibition of cholangiocarcinoma cells

Directory of Open Access Journals (Sweden)

Kwak TW

2017-10-01

Full Text Available Tae Won Kwak,1,* Hye Lim Lee,2,* Yeon Hui Song,2 Chan Kim,3 Jungsoo Kim,2 Sol-Ji Seo,2 Young-Il Jeong,2 Dae Hwan Kang2,4 1Medical Convergence Textile Center, Gyeongbuk, Republic of Korea; 2Biomedical Research Institute, Pusan National University Hospital, Pusan, Republic of Korea; 3Amogreentech Co. Ltd. Gyeonggi-do, Republic of Korea; 4Research Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Gyeongnam, Republic of Korea *These authors contributed equally to this work Purpose: The aim of this study was to fabricate a vorinostat (Zolinza™-eluting nanofiber membrane-coated gastrointestinal (GI stent and to study its antitumor activity against cholangiocarcinoma (CCA cells in vitro and in vivo. Methods: Vorinostat and poly(DL-lactide-co-glycolide dissolved in an organic solvent was sprayed onto a GI stent to make a nanofiber-coated stent using an electro-spinning machine. Intact vorinostat and vorinostat released from nanofibers was used to assess anticancer activity in vitro against various CCA cells. The antitumor activity of the vorinostat-eluting nanofiber membrane-coated stent was evaluated using HuCC-T1 bearing mice. Results: A vorinostat-incorporated polymer nanofiber membrane was formed on the surface of the GI stent. Vorinostat was continuously released from the nanofiber membrane over 10 days, and its release rate was higher in cell culture media than in phosphate-buffered saline. Released vorinostat showed similar anticancer activity against various CCA cells in vitro compared to that of vorinostat. Like vorinostat, vorinostat released from nanofibers induced acetylation of histone H4 and inhibited histone deacetylases 1·3·4/5/7 expression in vitro and in vivo. Furthermore, vorinostat nanofibers showed a higher tumor growth inhibition rate in HuCC-T1 bearing mice than vorinostat injections. Conclusion: Vorinostat-eluting nanofiber membranes showed significant antitumor

Mechanical, Thermal, and Morphological Properties of Nanocomposites Based on Polyvinyl Alcohol and Cellulose Nanofiber from Aloe vera Rind

Directory of Open Access Journals (Sweden)

Adel Ramezani Kakroodi

2014-01-01

Full Text Available This work was devoted to reinforcement of polyvinyl alcohol (PVA using cellulose nanofibers from Aloe vera rind. Nanofibers were isolated from Aloe vera rind in the form of an aqueous suspension using chemimechanical technique. Mechanical characterizations showed that incorporation of even small amounts of nanofibers (as low as 2% by weight had significant effects on both the modulus and strength of PVA. Tensile modulus and strength of PVA increased, 32 and 63%, respectively, after adding 2% of cellulose nanofiber from Aloe vera rind. Samples with higher concentrations of nanofibers also showed improved mechanical properties due to a high level of interfacial adhesion and also dispersion of fibers. The results showed that inclusion of nanofibers decreased deformability of PVA significantly. Dynamic mechanical analysis revealed that, at elevated temperatures, improvement of mechanical properties due to the presence of nanofibers was even more noticeable. Addition of nanofibers resulted in increased thermal stability of PVA in thermogravimetric analysis due to the reduction in mobility of matrix molecules. Morphological observations showed no signs of agglomeration of fibers even in composites with high cellulose nanofiber contents. Inclusion of nanofibers was shown to increase the density of composites.

In-situ Plasticized Cross-linked Polymer Composite Electrolyte Enhanced with Lithium-ion Conducting Nanofibers for Ambient All-Solid-State Lithium-ion Batteries

Energy Technology Data Exchange (ETDEWEB)

Yan, Chaoyi; Zhu, Pei; Jia, Hao; Zhu, Jiadeng; Selvan, R. Kalai; Li, Ya; Dong, Xia; Du, Zhuang; Angunawela, Indunil; Wu, Nianqiang; Dirican, Mahmut

2018-04-29

Solid electrolytes have been gaining attention recently for the development of next-generation Li-ion batteries due to the substantial improvements in stability and safety. Among various types of solid electrolytes, composite solid electrolytes (CSEs) exhibit both high ionic conductivity and excellent interfacial contact with the electrodes. Incorporating active nanofibers into the polymer matrix demonstrates an effective method to fabricate CSEs. However, current CSEs based on traditional poly(ethylene oxide) (PEO) polymer suffer from the poor ionic conductivity of PEO and agglomeration effect of inorganic fillers at high concentrations, which limit further improvements in Li+ conductivity and electrochemical stability. Herein, we synthesize a novel PEO based cross-linked polymer (CLP) as the polymer matrix with naturally amorphous structure and high room-temperature ionic conductivity of 2.40 × 10-4 S cm-1. Li0.3La0.557TiO3 (LLTO) nanofibers incorporated composite solid electrolytes (L-CLPCSE) exhibit enhanced ionic conductivity without showing filler agglomeration. The high content of Li-conductive nanofibers improves the mechanical strength, ensures the conductive networks, and increases the total Li+ conductivity to 3.31 × 10-4 S cm-1. The all-solid-state Li|LiFePO4 batteries with L-CLPCSE are able to deliver attractive specific capacity of 147 mAh g-1 at room temperature, and no evident dendrite is found at the anode/electrolyte interface after 100 cycles.

Fabrication of electrospun almond gum/PVA nanofibers as a thermostable delivery system for vanillin.

Science.gov (United States)

Rezaei, Atefe; Tavanai, Hossein; Nasirpour, Ali

2016-10-01

In this study, the fabrication of vanillin incorporated almond gum/polyvinyl alcohol (PVA) nanofibers through electrospinning has been investigated. Electrospinning of only almond gum was proved impossible. It was found that the aqueous solution of almond gum/PVA (80:20, concentration=7% (w/w)) containing 3% (w/w) vanillin could have successfully electrospun to uniform nanofibers with diameters as low as 77nm. According to the thermal analysis, incorporated vanillin in almond gum/PVA nanofibers showed higher thermal stability than free vanillin, making this composite especially suitable for high temperature applications. XRD and FTIR analyses proved the presence of vanillin in the almond gum/PVA nanofibers. It was also found that vanillin was dispersed as big crystallites in the matrix of almond gum/PVA nanofibers. FTIR analysis showed almond gum and PVA had chemical cross-linking by etheric bonds between COH groups of almond gum and OH groups of PVA. Also, in the nanofibers, there were no major interaction between vanillin and either almond gum or PVA. Copyright © 2016 Elsevier B.V. All rights reserved.

Polylactic acid (PLA)/Silver-NP/VitaminE bionanocomposite electrospun nanofibers with antibacterial and antioxidant activity

Science.gov (United States)

Munteanu, Bogdanel Silvestru; Aytac, Zeynep; Pricope, Gina M.; Uyar, Tamer; Vasile, Cornelia

2014-10-01

The antibacterial property of silver nanoparticles (Ag-NPs) and the antioxidant activity of Vitamin E have been combined by incorporation of these two active components within polylactic acid (PLA) nanofibers via electrospinning (PLA/Ag-NP/VitaminE nanofibers). The morphological and structural characterizations of PLA/Ag-NP/VitaminE nanofibers were performed by Scanning Electron Microscopy (SEM), Transmission Electron Microscopy and X-ray diffraction. The average fiber diameter was 140 ± 60 nm, and the size of the Ag-NP was 2.7 ± 1.5 nm. PLA/Ag-NP/VitaminE nanofibers inhibited growth of Escherichia coli, Listeria monocytogenes and Salmonella typhymurium up to 100 %. The amount of released Ag ions from the nanofibers immersed in aqueous solution was determined by Inductively Coupled Plasma Mass Spectrometry, and it has been observed that the release of Ag ions was kept approximately constant after 10 days of immersion. The antioxidant activity of PLA/Ag-NP/VitaminE nanofibers was evaluated according to DPPH (2,2-diphenyl-1-picrylhydrazyl) method and determined as 94 %. The results of the tests on fresh apple and apple juice indicated that the PLA/Ag/VitaminE nanofiber membrane actively reduced the polyphenol oxidase activity. The multifunctional electrospun PLA nanofibers incorporating Ag-NP and Vitamin E may be quite applicable in food packaging due to the extremely large surface area of nanofibers along with antibacterial and antioxidant activities. These materials could find application in food industry as a potential preservative packaging for fruits and juices.

A review on electrospun nanofibers for oral drug delivery

OpenAIRE

Abbas Akhgari; Zahra Shakib; Setareh Sanati

2017-01-01

Nowadays, polymer nanofibers have gained attention due to remarkable characteristics such as high porosity and large surface area to volume ratio. Among their fabrication methods, electrospinning technique has been attracted as a simple and reproducible approach. It is a versatile, simple and cost-effective technique for the production of continuous nanofibers with acceptable characteristics such as high porosity, high surface area to volume ratio, high loading capacity and encapsulation effi...

Preparation and characterization of doped TiO2 nanofibers by coaxial electrospining combined with sol–gel process

International Nuclear Information System (INIS)

Tong, Haixia; Tao, Xican; Wu, Daoxin; Zhang, Xiongfei; Li, Dan; Zhang, Ling

2014-01-01

Graphical abstract: The surface of the precursor of Fe/TiO 2 nanofibers are smoother than that of Fe /TiO 2 nanofibers. After calcined at 500 °C, the tubers on the surface of the nanofibers become more obvious, and which also provides a direct proof for the dopant of Fe element. -- Highlights: • N, Fe, and W doped TiO 2 nanofibers have been fabricated by coaxial electrospining. • The dopant has obvious influences on the surface topographies and crystal structures. • Fe doping can make remarkable topography changes and easy formation of rutile TiO 2 . • The maximum doping amount of W in TiO 2 nanofibers is less than 10% under 500 °C. -- Abstract: N, Fe, and W doped TiO 2 nanofibers were fabricated by coaxial electrospining and directly annealing polyvinylpyrrolidone (PVP)/Tetrabutyl titanate (TBT) composite nanofibers. The crystal structure, morphology, and surface composition of the doped TiO 2 nanofibers were investigated by the X-ray diffraction (XRD), scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS) respectively. The results show that the dopants have different influence on the surface topographies, the crystal structures and the transformation of anatase to rutile of TiO 2 nanofibers. Fe dopant promotes bigger influence on topographies, phase transformation and crystallite growth of TiO 2 nanofibers than that of either N or W dopant

Effect of Carbon Nanofiber-Matrix Adhesion on Polymeric Nanocomposite Properties—Part II

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Khalid Lafdi

2008-01-01

carbon nanocomposite. Carbon nanofibers were subjected to electrochemical oxidation in 0.1 M nitric acid for varying times. The strength of adhesion between the nanofiber and an epoxy matrix was characterized by flexural strength and modulus. The surface functional groups formed and their concentration of nanofibers showed a dependence on the degree of oxidation. The addition of chemical functional groups on the nanofiber surface allows them to physically and chemically adhere to the continuous resin matrix. The chemical interaction with the continuous epoxy matrix results in the creation of an interphase region. The ability to chemically and physically interact with the epoxy region is beneficial to the mechanical properties of a carbon nanocomposite. A tailored degree of surface functionalization was found to increase adhesion to the matrix and increase flexural modulus.

A novel electrospun hydroxypropyl methylcellulose/polyethylene oxide blend nanofibers: Morphology and physicochemical properties.

Science.gov (United States)

Aydogdu, Ayca; Sumnu, Gulum; Sahin, Serpil

2018-02-01

The objective of this study was to fabricate and characterize Hydroxypropyl methylcellulose (HPMC) -based homogenous nanofibers by using electrospinning method. As the concentrations of the solutions increased, viscosity and electrical conductivity of the solutions increased. The morphology of the fibers changed from the beaded structure to the uniform fiber structure by increasing the concentrations of the solutions. Water vapor permeability (WVP) of electrospun HPMC nanofibers decreased with increasing polymer concentration. The shift in wavelengths, the change in intensity of FTIR peaks and melting point depression were the evidence of miscibility of HPMC/PEO blends. Nanofibers showing both melting temperature (T m ) and glass transition temperature (T g ) had semicrystalline structure. By combining PEO with HPMC, the thermal stability of nanofibers was increased. Hence, this study suggests homogenous biopolymer-based nanofibers with low WVP and high thermal stability which can have potential applications in food packaging field. Copyright © 2017 Elsevier Ltd. All rights reserved.

Biotemplated preparation of CdS nanoparticles/bacterial cellulose hybrid nanofibers for photocatalysis application

International Nuclear Information System (INIS)

Yang, Jiazhi; Yu, Junwei; Fan, Jun; Sun, Dongping; Tang, Weihua; Yang, Xuejie

2011-01-01

In this work, we describe a novel facile and effective strategy to prepare micrometer-long hybrid nanofibers by deposition of CdS nanoparticles onto the substrate of hydrated bacterial cellulose nanofibers (BCF). Hexagonal phase CdS nanocrystals were achieved via a simple hydrothermal reaction between CdCl 2 and thiourea at relatively low temperature. The prepared pristine BCF and the CdS/BCF hybrid nanofibers were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), thermogravimetric analysis (TGA), UV-vis absorption spectroscopy (UV-vis), and X-ray photoelectron spectroscopy (XPS). The results reveal that the CdS nanoparticles were homogeneously deposited on the BCF surface and stabilized via coordination effect. The CdS/BCF hybrid nanofibers demonstrated high-efficiency photocatalysis with 82% methyl orange (MO) degradation after 90 min irradiation and good recyclability. The results indicate that the CdS/BCF hybrid nanofibers are promising candidate as robust visible light responsive photocatalysts.

Biotemplated preparation of CdS nanoparticles/bacterial cellulose hybrid nanofibers for photocatalysis application.

Science.gov (United States)

Yang, Jiazhi; Yu, Junwei; Fan, Jun; Sun, Dongping; Tang, Weihua; Yang, Xuejie

2011-05-15

In this work, we describe a novel facile and effective strategy to prepare micrometer-long hybrid nanofibers by deposition of CdS nanoparticles onto the substrate of hydrated bacterial cellulose nanofibers (BCF). Hexagonal phase CdS nanocrystals were achieved via a simple hydrothermal reaction between CdCl(2) and thiourea at relatively low temperature. The prepared pristine BCF and the CdS/BCF hybrid nanofibers were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), thermogravimetric analysis (TGA), UV-vis absorption spectroscopy (UV-vis), and X-ray photoelectron spectroscopy (XPS). The results reveal that the CdS nanoparticles were homogeneously deposited on the BCF surface and stabilized via coordination effect. The CdS/BCF hybrid nanofibers demonstrated high-efficiency photocatalysis with 82% methyl orange (MO) degradation after 90 min irradiation and good recyclability. The results indicate that the CdS/BCF hybrid nanofibers are promising candidate as robust visible light responsive photocatalysts. Copyright © 2011 Elsevier B.V. All rights reserved.

Biotemplated preparation of CdS nanoparticles/bacterial cellulose hybrid nanofibers for photocatalysis application

Energy Technology Data Exchange (ETDEWEB)

Yang, Jiazhi; Yu, Junwei [Key Laboratory of Soft Chemistry and Functional Materials (Ministry of Education), Nanjing University of Science and Technology, Nanjing 210094 (China); Fan, Jun [School of Environment, Nanjing University, Nanjing 210093 (China); Sun, Dongping [Key Laboratory of Soft Chemistry and Functional Materials (Ministry of Education), Nanjing University of Science and Technology, Nanjing 210094 (China); Tang, Weihua [Key Laboratory of Soft Chemistry and Functional Materials (Ministry of Education), Nanjing University of Science and Technology, Nanjing 210094 (China); Yang, Xuejie [Key Laboratory of Soft Chemistry and Functional Materials (Ministry of Education), Nanjing University of Science and Technology, Nanjing 210094 (China)

2011-05-15

In this work, we describe a novel facile and effective strategy to prepare micrometer-long hybrid nanofibers by deposition of CdS nanoparticles onto the substrate of hydrated bacterial cellulose nanofibers (BCF). Hexagonal phase CdS nanocrystals were achieved via a simple hydrothermal reaction between CdCl{sub 2} and thiourea at relatively low temperature. The prepared pristine BCF and the CdS/BCF hybrid nanofibers were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), thermogravimetric analysis (TGA), UV-vis absorption spectroscopy (UV-vis), and X-ray photoelectron spectroscopy (XPS). The results reveal that the CdS nanoparticles were homogeneously deposited on the BCF surface and stabilized via coordination effect. The CdS/BCF hybrid nanofibers demonstrated high-efficiency photocatalysis with 82% methyl orange (MO) degradation after 90 min irradiation and good recyclability. The results indicate that the CdS/BCF hybrid nanofibers are promising candidate as robust visible light responsive photocatalysts.

A novel approach to fabricate silk nanofibers containing hydroxyapatite nanoparticles using a three-way stopcock connector

Science.gov (United States)

Sheikh, Faheem A.; Ju, Hyung Woo; Moon, Bo Mi; Park, Hyun Jung; Kim, Jung Ho; Lee, Ok Joo; Park, Chan Hum

2013-07-01

Electrospinning technique is commonly used to produce micro- and/or nanofibers, which utilizes electrical forces to produce polymeric fibers with diameters ranging from several micrometers down to few nanometers. Desirably, electrospun materials provide highly porous structure and appropriate pore size for initial cell attachment and proliferation and thereby enable the exchange of nutrients. Composite nanofibers consisting of silk and hydroxyapatite nanoparticles (HAp) (NPs) had been considered as an excellent choice due to their efficient biocompatibility and bone-mimicking properties. To prepare these nanofiber composites, it requires the use of acidic solutions which have serious consequences on the nature of both silk and HAp NPs. It is ideal to create these nanofibers using aqueous solutions in which the physicochemical nature of both materials can be retained. However, to create those nanofibers is often difficult to obtain because of the fact that aqueous solutions of silk and HAp NPs can precipitate before they can be ejected into fibers during the electrospinning process. In this work, we had successfully used a three-way stopcock connector to mix the two different solutions, and very shortly, this solution is ejected out to form nanofibers due to electric fields. Different blend ratios consisting HAp NPs had been electrospun into nanofibers. The physicochemical aspects of fabricated nanofiber had been characterized by different state of techniques like that of FE-SEM, EDS, TEM, TEM-EDS, TGA, FT-IR, and XRD. These characterization techniques revealed that HAp NPs can be easily introduced in silk nanofibers using a stopcock connector, and this method favorably preserves the intact nature of silk fibroin and HAp NPs. Moreover, nanofibers obtained by this strategy were tested for cell toxicity and cell attachment studies using NIH 3 T3 fibroblasts which indicated non-toxic behavior and good attachment of cells upon incubation in the presence of nanofibers.

Controllable synthesis of Zn{sub 2}TiO{sub 4}-carbon core/shell nanofibers with high photocatalytic performance

Energy Technology Data Exchange (ETDEWEB)

Zhang, Peng [Center for Advanced Optoelectronic Functional Materials Research, and Key Laboratory of UV Light-Emitting Materials and Technology of Ministry of Education, Northeast Normal University, 5268 Renmin Street, Changchun 130024 (China); Shao, Changlu, E-mail: clshao@nenu.edu.cn [Center for Advanced Optoelectronic Functional Materials Research, and Key Laboratory of UV Light-Emitting Materials and Technology of Ministry of Education, Northeast Normal University, 5268 Renmin Street, Changchun 130024 (China); Zhang, Mingyi; Guo, Zengcai; Mu, Jingbo; Zhang, Zhenyi; Zhang, Xin; Liang, Pingping; Liu, Yichun [Center for Advanced Optoelectronic Functional Materials Research, and Key Laboratory of UV Light-Emitting Materials and Technology of Ministry of Education, Northeast Normal University, 5268 Renmin Street, Changchun 130024 (China)

2012-08-30

Graphical abstract: We describe a controllable route to synthesize Zn{sub 2}TiO{sub 4}-carbon core/shell nanofibers with different thickness of carbon layers (from 2 to 8 nm) as high efficiency photocatalysts. Highlights: Black-Right-Pointing-Pointer Synthesis of Zn{sub 2}TiO{sub 4}-carbon nanofibers with different thickness of carbon layers. Black-Right-Pointing-Pointer Zn{sub 2}TiO{sub 4}-carbon NFs showed photocatalytic activity for the degradation of Rhodamine B. Black-Right-Pointing-Pointer Easy photocatalyst separation and reuse. Black-Right-Pointing-Pointer A general way to fabricate other carbon-coated core/shell photocatalysts. - Abstract: Zn{sub 2}TiO{sub 4}-carbon core/shell nanofibers (Zn{sub 2}TiO{sub 4}-C NFs) with different thickness of carbon layers (from 2 to 8 nm) were fabricated by combining the electrospinning technique and hydrothermal method. The results showed that a uniform carbon layer was formed around the electrospun Zn{sub 2}TiO{sub 4} nanofiber (Zn{sub 2}TiO{sub 4} NFs). By adjusting the hydrothermal fabrication parameters, the thickness of carbon layer varied linearly with the concentration of glucose. Furthermore, the core/shell structure formed between Zn{sub 2}TiO{sub 4} and carbon enhanced the charge separation of pure Zn{sub 2}TiO{sub 4} under ultraviolet excitation, as evidenced by photoluminescence spectra. The photocatalytic studies revealed that the Zn{sub 2}TiO{sub 4}-C NFs exhibited enhanced photocatalytic efficiency of photodegradation of Rhodamine B (RB) compared with the pure Zn{sub 2}TiO{sub 4} NFs under ultraviolet excitation, which might be attributed to the high separation efficiency of photogenerated electrons and holes based on the synergistic effect between carbon and Zn{sub 2}TiO{sub 4}. Notably, the Zn{sub 2}TiO{sub 4}-C NFs could be recycled easily by sedimentation without a decrease of the photocatalytic activity.

Dislocation Starvation and Exhaustion Hardening in Mo-alloy Nanofibers

Energy Technology Data Exchange (ETDEWEB)

Chisholm, Claire [University of California, Berkeley & LBNL; Bei, Hongbin [ORNL; Lowry, M. B. [University of California, Berkeley; Oh, Jason [Hysitron, Inc., MN; Asif, S.A. Syed [Hysitron, Inc., MN; Warren, O. [Hysitron, Inc., MN; Shan, Zhiwei [Xi' an Jiaotong University, China & Hysitron, Inc., MN; George, Easo P [ORNL; Minor, Andrew [University of California, Berkeley & LBNL

2012-01-01

The evolution of defects in Mo alloy nanofibers with initial dislocation densities ranging from 0 to 1.6 1014 m2 were studied using an in situ push-to-pull device in conjunction with a nanoindenter in a transmission electron microscope. Digital image correlation was used to determine stress and strain in local areas of deformation. When they had no initial dislocations the Mo alloy nanofibers suffered sudden catastrophic elongation following elastic deformation to ultrahigh stresses. At the other extreme fibers with a high dislocation density underwent sustained homogeneous deformation after yielding at much lower stresses. Between these two extremes nanofibers with intermediate dislocation densities demonstrated a clear exhaustion hardening behavior, where the progressive exhaustion of dislocations and dislocation sources increases the stress required to drive plasticity. This is consistent with the idea that mechanical size effects ( smaller is stronger ) are due to the fact that nanostructures usually have fewer defects that can operate at lower stresses. By monitoring the evolution of stress locally we find that exhaustion hardening causes the stress in the nanofibers to surpass the critical stress predicted for self-multiplication, supporting a plasticity mechanism that has been hypothesized to account for the rapid strain softening observed in nanoscale bcc materials at high stresses.

Complementary effects of two growth factors in multifunctionalized silk nanofibers for nerve reconstruction.

Directory of Open Access Journals (Sweden)

Tony M Dinis

Full Text Available With the aim of forming bioactive guides for peripheral nerve regeneration, silk fibroin was electrospun to obtain aligned nanofibers. These fibers were functionalized by incorporating Nerve Growth Factor (NGF and Ciliary NeuroTrophic Factor (CNTF during electrospinning. PC12 cells grown on the fibers confirmed the bioavailability and bioactivity of the NGF, which was not significantly released from the fibers. Primary neurons from rat dorsal root ganglia (DRGs were grown on the nanofibers and anchored to the fibers and grew in a directional fashion based on the fiber orientation, and as confirmed by growth cone morphology. These biofunctionalized nanofibers led to a 3-fold increase in neurite length at their contact, which was likely due to the NGF. Glial cell growth, alignment and migration were stimulated by the CNTF in the functionalized nanofibers. Organotypic culture of rat fetal DRGs confirmed the complementary effect of both growth factors in multifunctionalized nanofibers, which allowed glial cell migration, alignment and parallel axonal growth in structures resembling the 'bands of Bungner' found in situ. Graftable multi-channel conduits based on biofunctionalized aligned silk nanofibers were developed as an organized 3D scaffold. Our bioactive silk tubes thus represent new options for a biological and biocompatible nerve guidance conduit.

Capture of toxic radioactive and heavy metal ions from water by using titanate nanofibers

Energy Technology Data Exchange (ETDEWEB)

Xu, Jiasheng, E-mail: jiashengxu@bhu.edu.cn [Liaoning Province Key Laboratory for Synthesis and Application of Functional Compounds, College of Chemistry, Chemical Engineering and Food Safety, Center of Science and Technology Experiment, Bohai University, 19 Sci-tech Road, Jinzhou 121013 (China); Zhang, He; Zhang, Jie [Liaoning Province Key Laboratory for Synthesis and Application of Functional Compounds, College of Chemistry, Chemical Engineering and Food Safety, Center of Science and Technology Experiment, Bohai University, 19 Sci-tech Road, Jinzhou 121013 (China); Kim, Eui Jung [School of Chemical Engineering and Bioengineering, University of Ulsan, Ulsan 680-749 (Korea, Republic of)

2014-11-25

Highlights: • Three types of titanate nanofibers were prepared via a hydrothermal porcess. • These nanofibers show availability for removal of the toxic ions from water. • The equilibrium data were fitted well with the Langmuir model. - Abstract: Three types of titanate nanofibers (sodium titanate nanofibers (TNF-A), potassium/sodium titanate nanofibers (TNF-B), potassium titanate nanofibers (TNF-C)) were prepared via a hydrothermal treatment of anatase powders in different alkali solutions at 170 °C for 96 h, respectively. The as-prepared nanofibers have large specific surface area and show availability for the removal of radioactive and heavy metal ions from water system, such as Ba{sup 2+} (as substitute of {sup 226}Ra{sup 2+}) and Pb{sup 2+} ions. The TNF-A shows a better capacity in the removal of Ba{sup 2+} and Pb{sup 2+} than TNF-B and TNF-C. Structural characterization of the materials was performed with powder X-ray diffraction (XRD), scanning electron microscopy (SEM) equipped with energy dispersive spectrometer (EDS) and with inductively coupled plasma optical emission spectrometry (ICP-OES). It is found that the equilibrium data fit well with the Langmuir model. This study highlights that nanoparticles of inorganic ion exchangers with layered structure are potential materials for efficient removal of the toxic ions from contaminated water.

Controlled Bioactive Molecules Delivery Strategies for Tendon and Ligament Tissue Engineering using Polymeric Nanofibers.

Science.gov (United States)

Hiong Teh, Thomas Kok; Hong Goh, James Cho; Toh, Siew Lok

2015-01-01

The interest in polymeric nanofibers has escalated over the past decade given its promise as tissue engineering scaffolds that can mimic the nanoscale structure of the native extracellular matrix. With functionalization of the polymeric nanofibers using bioactive molecules, localized signaling moieties can be established for the attached cells, to stimulate desired biological effects and direct cellular or tissue response. The inherently high surface area per unit mass of polymeric nanofibers can enhance cell adhesion, bioactive molecules loading and release efficiencies, and mass transfer properties. In this review article, the application of polymeric nanofibers for controlled bioactive molecules delivery will be discussed, with a focus on tendon and ligament tissue engineering. Various polymeric materials of different mechanical and degradation properties will be presented along with the nanofiber fabrication techniques explored. The bioactive molecules of interest for tendon and ligament tissue engineering, including growth factors and small molecules, will also be reviewed and compared in terms of their nanofiber incorporation strategies and release profiles. This article will also highlight and compare various innovative strategies to control the release of bioactive molecules spatiotemporally and explore an emerging tissue engineering strategy involving controlled multiple bioactive molecules sequential release. Finally, the review article concludes with challenges and future trends in the innovation and development of bioactive molecules delivery using polymeric nanofibers for tendon and ligament tissue engineering.

Process Optimization and Emperical Modelling for Electrospun Polyacrylonitrile (PAN) Nanofiber Precursor of Carbon nanofibers

NARCIS (Netherlands)

Gu, S.Y.; Gu, S.; Ren, J.; Vancso, Gyula J.

2005-01-01

Ultrafine fibers were spun from polyacrylonitrile (PAN)/N,N-dimethyl formamide (DMF) solution as a precursor of carbon nanofibers using a homemade electrospinning set-up. Fibers with diameter ranging from 200 nm to 1200 nm were obtained. Morphology of fibers and distribution of fiber diameter were

Electrospun Nanofiber Scaffolds with Gradations in Fiber Organization

Science.gov (United States)

Khandalavala, Karl; Jiang, Jiang; Shuler, Franklin D.; Xie, Jingwei

2015-01-01

The goal of this protocol is to report a simple method for generating nanofiber scaffolds with gradations in fiber organization and test their possible applications in controlling cell morphology/orientation. Nanofiber organization is controlled with a new fabrication apparatus that enables the gradual decrease of fiber organization in a scaffold. Changing the alignment of fibers is achieved through decreasing deposition time of random electrospun fibers on a uniaxially aligned fiber mat. By covering the collector with a moving barrier/mask, along the same axis as fiber deposition, the organizational structure is easily controlled. For tissue engineering purposes, adipose-derived stem cells can be seeded to these scaffolds. Stem cells undergo morphological changes as a result of their position on the varied organizational structure, and can potentially differentiate into different cell types depending on their locations. Additionally, the graded organization of fibers enhances the biomimicry of nanofiber scaffolds so they more closely resemble the natural orientations of collagen nanofibers at tendon-to-bone insertion site compared to traditional scaffolds. Through nanoencapsulation, the gradated fibers also afford the possibility to construct chemical gradients in fiber scaffolds, and thereby further strengthen their potential applications in fast screening of cell-materials interaction and interfacial tissue regeneration. This technique enables the production of continuous gradient scaffolds, but it also can potentially produce fibers in discrete steps by controlling the movement of the moving barrier/mask in a discrete fashion. PMID:25938562

Fabrication and characterization of anisotropic nanofiber scaffolds for advanced drug delivery systems

Directory of Open Access Journals (Sweden)

Jalani G

2014-05-01

Full Text Available Ghulam Jalani,* Chan Woo Jung,* Jae Sang Lee, Dong Woo Lim Department of Bionano Engineering, College of Engineering Sciences, Hanyang University, Education Research Industry Cluster at Ansan Campus, Ansan, South Korea*These authors contributed equally to this workAbstract: Stimuli-responsive, polymer-based nanostructures with anisotropic compartments are of great interest as advanced materials because they are capable of switching their shape via environmentally-triggered conformational changes, while maintaining discrete compartments. In this study, a new class of stimuli-responsive, anisotropic nanofiber scaffolds with physically and chemically distinct compartments was prepared via electrohydrodynamic cojetting with side-by-side needle geometry. These nanofibers have a thermally responsive, physically-crosslinked compartment, and a chemically-crosslinked compartment at the nanoscale. The thermally responsive compartment is composed of physically crosslinkable poly(N-isopropylacrylamide poly(NIPAM copolymers, and poly(NIPAM-co-stearyl acrylate poly(NIPAM-co-SA, while the thermally-unresponsive compartment is composed of polyethylene glycol dimethacrylates. The two distinct compartments were physically crosslinked by the hydrophobic interaction of the stearyl chains of poly(NIPAM-co-SA or chemically stabilized via ultraviolet irradiation, and were swollen in physiologically relevant buffers due to their hydrophilic polymer networks. Bicompartmental nanofibers with the physically-crosslinked network of the poly(NIPAM-co-SA compartment showed a thermally-triggered shape change due to thermally-induced aggregation of poly(NIPAM-co-SA. Furthermore, when bovine serum albumin and dexamethasone phosphate were separately loaded into each compartment, the bicompartmental nanofibers with anisotropic actuation exhibited decoupled, controlled release profiles of both drugs in response to a temperature. A new class of multicompartmental nanofibers could be

Pulsed laser dewetting of nickel catalyst for carbon nanofiber growth

International Nuclear Information System (INIS)

Guan, Y F; Pearce, R C; Simpson, M L; Rack, P D; Melechko, A V; Hensley, D K

2008-01-01

We present a pulsed laser dewetting technique that produces single nickel catalyst particles from lithographically patterned disks for subsequent carbon nanofiber growth through plasma enhanced chemical vapor deposition. Unlike the case for standard heat treated Ni catalyst disks, for which multiple nickel particles and consequently multiple carbon nanofibers (CNFs) are observed, single vertically aligned CNFs could be obtained from the laser dewetted catalyst. Different laser dewetting parameters were tested in this study, such as the laser energy density and the laser processing time measured by the total number of laser pulses. Various nickel disk radii and thicknesses were attempted and the resultant number of carbon nanofibers was found to be a function of the initial disk dimension and the number of laser pulses

Polyamic Acid Nanofibers Produced by Needleless Electrospinning

Directory of Open Access Journals (Sweden)

Oldrich Jirsak

2010-01-01

Full Text Available The polyimide precursor (polyamic acid produced of 4,4′-oxydiphthalic anhydride and 4,4′-oxydianiline was electrospun using needleless electrospinning method. Nonwoven layers consisting of submicron fibers with diameters in the range about 143–470 nm on the polypropylene spunbond supporting web were produced. Filtration properties of these nanofiber layers on the highly permeable polypropylene support—namely filtration effectivity and pressure drop—were evaluated. Consequently, these polyamic acid fibers were heated to receive polyimide nanofibers. The imidization process has been studied using IR spectroscopy. Some comparisons with the chemically identical polyimide prepared as the film were made.

Thermally driven self-healing using copper nanofiber heater

Science.gov (United States)

Lee, Min Wook; Jo, Hong Seok; Yoon, Sam S.; Yarin, Alexander L.

2017-07-01

Nano-textured transparent heaters made of copper nanofibers (CuNFs) are used to facilitate accelerated self-healing of bromobutyl rubber (BIIR). The heater and BIIR layer are separately deposited on each side of a transparent flexible polyethylene terephthalate (PET) substrate. A pre-notched crack on the BIIR layer was bridged due to heating facilitated by CuNFs. In the corrosion test, a cracked BIIR layer covered a steel substrate. An accelerated self-healing of the crack due to the transparent copper nanofiber heater facilitated an anti-corrosion protective effect of the BIIR layer.

Electrospun Xanthan gum-Chitosan nanofibers as delivery carrier of hydrophobic bioactives

DEFF Research Database (Denmark)

Shekarforoush, Elhamalsadat; Ajalloueian, Fatemeh; Zeng, Guanghong

2018-01-01

Viscoelastic gels of xanthan gum-chitosan(X-Ch) were electrospun to produce nanofibers, stable in aqueous media, for the encapsulation and release of curcumin (Cu). After 120h, the nanofibers released lower amount of curcumin (∼20%) at pH 2.2 comparatively to the release in neutral media (∼50...

Osteoinductive peptide-functionalized nanofibers with highly ordered structure as biomimetic scaffolds for bone tissue engineering

Directory of Open Access Journals (Sweden)

Gao X

2015-11-01

Full Text Available Xiang Gao,1,2,* Xiaohong Zhang,3,* Jinlin Song,1,2 Xiao Xu,4 Anxiu Xu,1 Mengke Wang,4 Bingwu Xie,1 Enyi Huang,2 Feng Deng,1,2 Shicheng Wei2–41College of Stomatology, 2Chongqing Key Laboratory of Oral Diseases and Biomedical Sciences, Chongqing Medical University, Chongqing, 3Center for Biomedical Materials and Tissue Engineering, Academy for Advanced Interdisciplinary Studies, Peking University, 4Department of Oral and Maxillofacial Surgery, Laboratory of Interdisciplinary Studies, Peking University School and Hospital of Stomatology, Beijing, People’s Republic of China*These authors contributed equally to this workAbstract: The construction of functional biomimetic scaffolds that recapitulate the topographical and biochemical features of bone tissue extracellular matrix is now of topical interest in bone tissue engineering. In this study, a novel surface-functionalized electrospun polycaprolactone (PCL nanofiber scaffold with highly ordered structure was developed to simulate the critical features of native bone tissue via a single step of catechol chemistry. Specially, under slightly alkaline aqueous solution, polydopamine (pDA was coated on the surface of aligned PCL nanofibers after electrospinning, followed by covalent immobilization of bone morphogenetic protein-7-derived peptides onto the pDA-coated nanofiber surface. Contact angle measurement, Raman spectroscopy, and X-ray photoelectron spectroscopy confirmed the presence of pDA and peptides on PCL nanofiber surface. Our results demonstrated that surface modification with osteoinductive peptides could improve cytocompatibility of nanofibers in terms of cell adhesion, spreading, and proliferation. Most importantly, Alizarin Red S staining, quantitative real-time polymerase chain reaction, immunostaining, and Western blot revealed that human mesenchymal stem cells cultured on aligned nanofibers with osteoinductive peptides exhibited enhanced osteogenic differentiation potential than

Nanobiotechnology approach to fabricate polycaprolactone nanofibers containing solid titanium nanoparticles as future implant materials

DEFF Research Database (Denmark)

Sheikh, Faheem A.; Kanjwal, Muzafar Ahmed; Cha, Jaegwan

2011-01-01

In this study, a good combination of electrospun poly(caprolactone) nanofibers incorporated with high purity titanium nanoparticles is introduced for hard tissue engineering applications. A simple approach to utilize the colloidal properties of poly(caprolactone) and titanium nanoparticles...... nanofiber mats, they were incubated in simulated body fluid at 37 °C for 10 days. Field emission scanning electron microscopy in combination with energy-dispersive X-ray spectroscopy indicated that incorporation of titanium strongly activates precipitation of the apatite-like materials from the utilized...... simulated body fluid. Moreover, in-vivo experiments using experimental dogs revealed that nanofibers can yield good tissue regeneration on the surfaces of nanofibers....