scholarly journals Evaluation of the Morphology and Osteogenic Potential of Titania-Based Electrospun Nanofibers

2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Xiaokun Wang ◽  
Jingxian Zhu ◽  
Ling Yin ◽  
Shize Liu ◽  
Xin Zhang ◽  
...  
Keyword(s):  
Sol Gel ◽  
Polymer Concentration ◽  
Electrospun Nanofibers ◽  
Average Diameter ◽  
Cell Number ◽  
Crystal Phase ◽  
Osteogenic Potential ◽  
Ceramic Fibers ◽  
Submicron Scale ◽  
Differentiation Marker

Submicron-scale titania-based ceramic fibers with various compositions have been prepared by electrospinning. The as-prepared nanofibers were heat-treated at 700°C for 3 h to obtain pure inorganic fiber meshes. The results show that the diameter and morphology of the nanofibers are affected by starting polymer concentration and sol-gel composition. The titania and titania-silica nanofibers had the average diameter about 100–300 nm. The crystal phase varied from high-crystallized rutile-anatase mixed crystal to low-crystallized anatase with adding the silica addition. The morphology and crystal phase were evaluated by SEM and XRD. Bone-marrow-derived mesenchymal stem cells were seeded on titania-silica 50/50 fiber meshes. Cell number and early differentiation marker expressions were analyzed, and the results indicated osteogenic potential of the titania-silica 50/50 fiber meshes.

scholarly journals Optimized Loading of TiO2 Nanoparticles into Electrospun Polyacrylonitrile and Cellulose Acetate Polymer Fibers

2020 ◽  
Vol 2020 ◽  
pp. 1-10
Author(s):  
Sibongile C. Nkabinde ◽  
Makwena J. Moloto ◽  
Kgabo P. Matabola
Keyword(s):  
Cellulose Acetate ◽  
Anatase Phase ◽  
Sol Gel ◽  
Polymer Concentration ◽  
Emission Spectra ◽  
Average Diameter ◽  
Xrd Analysis ◽  
Polymer Fibers ◽  
Electrospinning Technique ◽  
Calcination Temperatures

Polyacrylonitrile (PAN), cellulose acetate (CA), PAN-TiO2, and CA-TiO2 nanofibers were prepared using the electrospinning technique under varying the loading of the TiO2 nanoparticles. The latter TiO2 nanoparticles were prepared using the sol-gel method by varying the calcination temperatures. The absorption and emission spectra illustrated the formation of TiO2 nanoparticles with an increase in absorption band edges with smaller particles. The TEM results showed the spherical morphology of the nanoparticles calcined at 500°C with an average diameter of 12.2±3.3 nm. XRD analysis revealed anatase phase as the dominant crystalline phase of the nanoparticles. TiO2 nanoparticle loadings of 0.2 and 0.4 wt% were incorporated into 16 wt% CA solutions while 1, 2, and 3 wt% of TiO2 nanoparticles were incorporated into 10 wt% PAN solutions. The SEM results illustrated the lowering in diameter and morphology of the nanofibers upon incorporation of nanoparticles. Their respective average diameters are 220, 338, 181, and 250 nm for PAN, CA, PAN-TiO2, and CA-TiO2 polymer fibers, respectively. The morphology of the nanofibers improved while the diameter increased with an increase in polymer concentration. Different loadings of TiO2 nanoparticles improved the electrospinnability and morphology and further decreased the size of the nanofibers. FTIR spectroscopy signifies the formation of nanocomposites and the presence of TiO2 nanoparticles which corresponded to the Ti-O stretching and Ti-O-Ti bands on the FTIR spectra.

scholarly journals Electrospun PVP/TiO2 Nanofibers for Filtration and Possible Protection from Various Viruses Like COVID-19

Technologies ◽  
2021 ◽  
Vol 9 (4) ◽  
pp. 89
Author(s):  
Ankush Sharma ◽  
Dinesh Pathak ◽  
Deepak S. Patil ◽  
Naresh Dhiman ◽  
Viplove Bhullar ◽  
...  
Keyword(s):  
Environmental Remediation ◽  
Low Cost ◽  
Sol Gel ◽  
Polymer Concentration ◽  
Volume Ratio ◽  
Electrospun Nanofibers ◽  
Test Surface ◽  
Sem Images ◽  
Electrospinning Technique ◽  
Tio2 Nanofibers

In this study, TiO2 nanofibers were prepared with Polyvinylpyrrolidone (PVP) polymer using sol-gel method via electrospinning technique. Owing to the advantages of small fiber diameter, tunable porosity, low cost, large surface to volume ratio, structure control, light-weight, and less energy consumption, electrospun nanofibers are evolving as an adaptable material with a number of applications, in this case for filtration and environmental/virus protection. Different samples of TiO2/PVP nanofibers have been prepared by changing the parameters to achieve the best result. As the polymer concentration was increased from 6 to 8 wt.% of PVP, diameter of the resultant fibers was seen to be increased, implying decrease in the pore-size of the fibers up to 1.4 nm. Surface morphology has been checked via Scanning Electron Microscope (SEM) images. Crystalline nature has been analyzed by X-Ray Crystallography. Using the Bruanauer-Emmett-Teller (BET) test, surface area and porosity has been checked for the suitable application. The synthesized TiO2/PVP nanofibers have tremendous practical potentials in filtration and environmental remediation applications.

Solution Electrospinning of Nylon/Ferrite Nanofibers

2003 ◽  
Vol 788 ◽  
Author(s):  
Autumn Dhanote ◽  
Samuel C. Ugbolue ◽  
Steven B. Warner ◽  
Prabir K. Patra ◽  
Phaneshwar Katangur ◽  
...  
Keyword(s):  
Polymer Solution ◽  
Polymer Concentration ◽  
Polymer System ◽  
Electrospun Nanofibers ◽  
Average Diameter ◽  
Particle Dispersion ◽  
Ferrite Nanoparticles ◽  
Diameter Distribution ◽  
Benzene Sulfonic Acid ◽  
Solution Electrospinning

ABSTRACTWith an average diameter of 80–200 nm, nylon fibers embedded with ferrite nanoparticles were electrospun using a point to plate geometry. The nickel-ferrite particles with a diameter range of 20–30 nm were used to prepare the composite electrospun nanofibers. The ferrite nanoparticles were dispersed in the polymer solution using a surfactant dodecyl benzene sulfonic acid (DBSA). Ultrasonication was used to dissolve nylon-6 into the formic acid/particle dispersion. Electrospinning of virgin polymer solution and particle filled polymer system was carried out with polymer concentration of 15% w/v. The particle loading was 3%w/w. SEM of the particle filled fibers show some bead formations and a diameter distribution of about 80–200 nm. The DSC analyses of the neat nylon polymer fibers and ferrite filled nanofibers show an increase in glass transition temperature from 55°C to 72°C. The melting temperature showed a decrease from 226°C to 201°C. The TEM images show the presence and some alignment of particles in the polymer. The electron diffraction pattern of ferrite nanoparticles confirms its crystalline nature.

Efficient Micromixing for Continuous Biodiesel Production from Jatropha Oil

2018 ◽  
Vol 9 (1) ◽  
pp. 133-139
Author(s):  
Waleed S. Mohammed ◽  
Ahmed H. El-Shazly ◽  
Marwa F. Elkady ◽  
Masahiro Ohshima
Keyword(s):  
Methyl Esters ◽  
Continuous Process ◽  
Sol Gel ◽  
Average Diameter ◽  
Biodiesel Production ◽  
High Mass ◽  
Molar Ratio ◽  
Jatropha Oil ◽  
Energy Deficiency ◽  
Gel Preparation

Introduction: The utilization of biodiesel as an alternative fuel is turning out to be progressively famous these days because of worldwide energy deficiency. The enthusiasm for utilizing Jatropha as a non-edible oil feedstock is quickly developing. The performance of the base catalyzed methanolysis reaction could be improved by a continuous process through a microreactor in view of the high mass transfer coefficient of this technique. Materials & Methods: Nanozirconium tungstovanadate, which was synthetized using sol-gel preparation method, was utilized in a complementary step for biodiesel production process. The prepared material has an average diameter of 0.066 &µm. Results: First, the NaOH catalyzed methanolysis of Jatropha oil was investigated in a continuous microreactor, and the efficient mixing over different mixers and its impact on the biodiesel yield were studied under varied conditions. Second, the effect of adding the nanocatalyst as a second stage was investigated. Conclusion: The maximum percentage of produced methyl esters from Jatropha oil was 98.1% using a methanol/Jatropha oil molar ratio of 11 within 94 s using 1% NaOH at 60 &°C. The same maximum conversion ratio was recorded with the nanocatalyst via only 0.3% NaOH.

Enhanced Skin Permeation of Punicalagin after Topical Application of Pluronic Micelles or Vesicles Loaded with Lafoensia pacari Extract

Planta Medica ◽  
2021 ◽  
Author(s):  
Sandra Alves de Sousa Garcia ◽  
Priscila Bianca Rodrigues da Rocha ◽  
Bruno dos Santos Souza ◽  
Andressa Tuane Santana Paz ◽  
Ana Luiza Caetano Negris ◽  
...  
Keyword(s):  
Antioxidant Activity ◽  
Skin Permeation ◽  
Sol Gel ◽  
Extraction Procedure ◽  
Average Diameter ◽  
Skin Aging ◽  
Chemical Degradation ◽  
Vertical Diffusion ◽  
Flowing Liquid ◽  
Span 80

AbstractPunicalagin, the principal ellagitannin of Lafoensia pacari leaves, has proven antioxidant activity, and standardized extracts of L. pacari can be topically used for skin aging management. We hypothesized that Pluronic nanomicelles or vesicles could solubilize sufficiently large amounts of the standardized extracts of L. pacari and provide chemical stability to punicalagin. The standardized extracts of L. pacari were obtained with an optimized extraction procedure, and the antioxidant activity was characterized. Formulations containing Pluronic at 25% and 35% were obtained with or without Span 80. They were characterized by average diameter, polydispersity index, punicalagin content, physicochemical stability, and rheology. A release and skin permeation study was carried out in vertical diffusion cells. The extraction procedure allowed quantifying high punicalagin content (i.e., 141.61 ± 3.87 mg/g). The standardized extracts of L. pacari showed antioxidant activity for all evaluated methods. Pluronic at 25 and Pluronic at 35 with standardized extracts of L. pacari showed an average diameter of about 25 nm. The addition of Span 80 significantly increased the mean diameter by 15-fold (p < 0.05), indicating the spontaneous formation of vesicles. Pluronic formulations significantly protected punicalagin from chemical degradation (p < 0.05). Pluronic at 25 formulations presented as free-flowing liquid-like systems, while Pluronic at 35 resulted in an increase of about 44-fold in |ƞ*|. The addition of Span 80 significantly reduced the Pluronic sol-gel transition temperature (p < 0.05), indicating the formation of vesicles. Formulations with Span 80 significantly enhanced punicalagin skin permeation compared to formulations without Span 80 (p < 0.05). Formulations with Span 80 were demonstrated to be the most promising formulations, as they allowed significant permeation of punicalagin (about 80 to 315 µg/cm2), which has been shown to have antioxidant activity.

scholarly journals Fabrication and Characterization of Electrospun Poly(acrylonitrile-co-Methyl Acrylate)/Lignin Nanofibers: Effects of Lignin Type and Total Polymer Concentration

Polymers ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 992
Author(s):  
Suchitha Devadas ◽  
Saja M. Nabat Al-Ajrash ◽  
Donald A. Klosterman ◽  
Kenya M. Crosson ◽  
Garry S. Crosson ◽  
...  
Keyword(s):  
Methyl Acrylate ◽  
Lignin Content ◽  
Polymer Concentration ◽  
Weight Ratio ◽  
Electrospun Nanofibers ◽  
Polymer Content ◽  
Blend Ratio ◽  
Blend Ratios ◽  
Poly Acrylonitrile

Lignin macromolecules are potential precursor materials for producing electrospun nanofibers for composite applications. However, little is known about the effect of lignin type and blend ratios with synthetic polymers. This study analyzed blends of poly(acrylonitrile-co-methyl acrylate) (PAN-MA) with two types of commercially available lignin, low sulfonate (LSL) and alkali, kraft lignin (AL), in DMF solvent. The electrospinning and polymer blend solution conditions were optimized to produce thermally stable, smooth lignin-based nanofibers with total polymer content of up to 20 wt % in solution and a 50/50 blend weight ratio. Microscopy studies revealed that AL blends possess good solubility, miscibility, and dispersibility compared to LSL blends. Despite the lignin content or type, rheological studies demonstrated that PAN-MA concentration in solution dictated the blend’s viscosity. Smooth electrospun nanofibers were fabricated using AL depending upon the total polymer content and blend ratio. AL’s addition to PAN-MA did not affect the glass transition or degradation temperatures of the nanofibers compared to neat PAN-MA. We confirmed the presence of each lignin type within PAN-MA nanofibers through infrared spectroscopy. PAN-MA/AL nanofibers possessed similar morphological and thermal properties as PAN-MA; thus, these lignin-based nanofibers can replace PAN in future applications, including production of carbon fibers and supercapacitors.

scholarly journals Fast Dissolving Electrospun Nanofibers Fabricated from Jelly Fig Polysaccharide/Pullulan for Drug Delivery Applications

Polymers ◽  
2021 ◽  
Vol 13 (2) ◽  
pp. 241
Author(s):  
Thangavel Ponrasu ◽  
Bei-Hsin Chen ◽  
Tzung-Han Chou ◽  
Jia-Jiuan Wu ◽  
Yu-Shen Cheng
Keyword(s):  
Drug Delivery ◽  
Water Vapor Permeability ◽  
Electrospun Nanofibers ◽  
Average Diameter ◽  
Xrd Analysis ◽  
Water Soluble ◽  
Vapor Permeability ◽  
Uv Spectrum ◽  
Sem Images ◽  
Triton X

The fast-dissolving drug delivery systems (FDDDSs) are developed as nanofibers using food-grade water-soluble hydrophilic biopolymers that can disintegrate fast in the oral cavity and deliver drugs. Jelly fig polysaccharide (JFP) and pullulan were blended to prepare fast-dissolving nanofiber by electrospinning. The continuous and uniform nanofibers were produced from the solution of 1% (w/w) JFP, 12% (w/w) pullulan, and 1 wt% Triton X-305. The SEM images confirmed that the prepared nanofibers exhibited uniform morphology with an average diameter of 144 ± 19 nm. The inclusion of JFP in pullulan was confirmed by TGA and FTIR studies. XRD analysis revealed that the increased crystallinity of JFP/pullulan nanofiber was observed due to the formation of intermolecular hydrogen bonds. The tensile strength and water vapor permeability of the JFP/pullulan nanofiber membrane were also enhanced considerably compared to pullulan nanofiber. The JFP/pullulan nanofibers loaded with hydrophobic model drugs like ampicillin and dexamethasone were rapidly dissolved in water within 60 s and release the encapsulants dispersive into the surrounding. The antibacterial activity, fast disintegration properties of the JFP/pullulan nanofiber were also confirmed by the zone of inhibition and UV spectrum studies. Hence, JFP/pullulan nanofibers could be a promising carrier to encapsulate hydrophobic drugs for fast-dissolving/disintegrating delivery applications.

Effect of pH Value on the Synthesis of NiO Nanoparticles and Microstructure of NiO Based Composite Anode

2021 ◽  
Vol 317 ◽  
pp. 447-453
Author(s):  
Noor Hidayah Aniza Zakaria ◽  
Nafisah Osman
Keyword(s):  
Ph Value ◽  
Sol Gel ◽  
Secondary Phase ◽  
Average Diameter ◽  
Morphological Observation ◽  
Nio Nanoparticles ◽  
Composite Anode ◽  
Ph Values ◽  
Particle Size Analyzer ◽  
Nio Nps

NiO nanoparticle was synthesized by a sol-gel method with three different pH values namely pH=1, 7 and 11, and then calcined at temperature of 450 ᵒC. The influence of different pH values on the physical properties of NiO nanoparticles were investigated by a particle size analyzer (PSA), field emission scanning electron microscope (FESEM) and X-ray diffractometer (XRD). Structural analysis confirmed that a cubic structure of NiO nanoparticle was obtained without any secondary phase for NiO powders prepared with pH=1, while the peak of secondary phase (Ni) appeared for NiO powders prepared with pH= 7 and 11. Morphological observation showed that the NiO nanoparticles prepared with pH=7 and 11 tend to form more agglomerates compared to one prepared with pH=1. The average diameter of NiO nanoparticles with pH 1, 7 and 11 were approximately in the range of 19-26 nm, 21-28 nm, and 24-30 nm, respectively. NiO powder that was synthesized with pH=1 was further used to prepare composite anode of NiO Nps-BaCe0.54Zr0.36Y0.1O2.95 (BCZY) powder. Unfortunately a composite of NiO Nps-BaCeO3-BaZrO3 was obtained instead of BCZY and governed by agglomerates with size in the range of 70-300 nm.

Formation of aramid-silica-grafted-multi-walled carbon nanotube-based nanofiber via the sol-gel route: thermal and mechanical profile of hybrids with poly(methyl methacrylate)

e-Polymers ◽  
2014 ◽  
Vol 14 (3) ◽  
pp. 177-185
Author(s):  
Ayesha Kausar
Keyword(s):  
Carbon Nanotube ◽  
Methyl Methacrylate ◽  
Sol Gel ◽  
Tensile Modulus ◽  
Electrospun Nanofibers ◽  
Decomposition Temperature ◽  
Filler Loading ◽  
Silica Network ◽  
Poly Methyl Methacrylate ◽  
Multi Walled Carbon Nanotube

AbstractIn this study, thermally and mechanically stable poly(methyl methacrylate) (PMMA)-based nanocomposites were produced through the reinforcement of electrospun aramid-silica-grafted multi-walled carbon nanotube-based nanofibers (MWCNT-Ar-Si). The multi-walled carbon nanotube was initially modified to prepare an isocyanatopropyltriethoxysilane-grafted MWCNT via the sol-gel route using 3-isocyanatopropyl-triethoxysilane and tetraethoxysilane (TEOS). The silica network was developed and linked to MWCNT by hydrolysis and condensation of TEOS. The said isocyanatopropyltriethoxysilane-grafted MWCNT was electrospun with the aramid solution. The electrospun MWCNT-Ar-Si nanofibers (0.1–1 wt.%) were then reinforced in a PMMA matrix. For comparative analysis, PMMA was also reinforced with 0.1–1 wt.% of aramid nanofibers. The tensile modulus of PMMA/MWCNT-Ar-Si 0.1 was 5.11 GPa, which was increased to 13.1 GPa in PMMA/MWCNT-Ar-Si 1. The 10% decomposition temperature of PMMA/MWCNT-Ar-Si 0.1–1 hybrids was in the range of 479–531°C. The glass transition temperature, determined from the maxima of tan δ data using dynamic mechanical thermal analysis, showed an increase with the filler loading and was maximum (301°C) for PMMA/MWCNT-Ar-Si 1 with 1 wt.% of MWCNT-Ar-Si nanofibers. In contrast, PMMA/Ar 0.1–1 hybrids showed lower values in the thermal and the mechanical profile depicting the combined effect of nanotube and aramid in electrospun nanofibers.

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