Polycaprolactone/α-Alumina and Hydroxyapatite-based Micro- and Nano- Structured Hybrid Fibers

2013 ◽  
Vol 1569 ◽  
pp. 185-191 ◽  
Author(s):  
Simón Y. Reyes-Lopéz ◽  
Bonifacio Alvarado-Tenorio ◽  
Ángel Romo-Uribe
Keyword(s):  
Structural Model ◽  
Polarized Light ◽  
Inorganic Nanoparticles ◽  
Alumina Nanoparticles ◽  
Size Analysis ◽  
Hybrid Fibers ◽  
Scanning Calorimetry ◽  
Transmission Electron ◽  
Average Size ◽  
20 Nm

ABSTRACTThe micro- and nanostructured phase behavior of non-woven hybrid electrospun fibers of Polycaprolactone (PCL-f), Polycaprolactone/α-Alumina (PCL/AA) and Polycaprolactone/Hydroxyapatite (PCL/HA) were elucidated. Nanoparticles of Hydroxyapatite featured 7-20 nm while α-Alumina was 500 nm in average size. Analysis by Transmission Electron Microscopy (TEM), Small-Angle Light Scattering (SALS), Polarized Optical Microscopy (POM) and Differential Scanning Calorimetry (DSC) enabled us to suggest a simple structural model for the series of hybrid fibers. PCL with a molecular weight of 70,000 g/mol was dissolved in chloroform. POM exhibited qualitative birefringent regions for all samples at the microscale level. Furthermore, polarized light distinguished between amorphous and micro-ordered structures along the fibers. On the other hand, SALS patterns suggested a needle-like morphology for all fibers. The influence of both, Hydroxyapatite and α-Alumina, was apparent in the SALS patterns of the PCL semicrystalline phase. Thermal analysis by DSC showed that the crystalline phase of PCL was disrupted by the presence of the inorganic nanoparticles. TEM micrographs showed that Hydroxyapatite and α-Alumina nanoparticles were embedded along the structure of PCL microfibers.

scholarly journals Study on Structure, Thermal Behavior, and Viscoelastic Properties of Nanodiamond-Reinforced Poly (vinyl alcohol) Nanocomposites

Polymers ◽  
2021 ◽  
Vol 13 (9) ◽  
pp. 1426
Author(s):  
Tomáš Remiš ◽  
Petr Bělský ◽  
Tomáš Kovářík ◽  
Jaroslav Kadlec ◽  
Mina Ghafouri Azar ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Mechanical Analysis ◽  
Single Step ◽  
Poly Vinyl Alcohol ◽  
Scanning Calorimetry ◽  
X Ray Scattering ◽  
Transmission Electron ◽  
Primary Particles ◽  
Solution Casting Method ◽  
Average Size

In this work, advanced polymer nanocomposites comprising of polyvinyl alcohol (PVA) and nanodiamonds (NDs) were developed using a single-step solution-casting method. The properties of the prepared PVA/NDs nanocomposites were investigated using Raman spectroscopy, small- and wide-angle X-ray scattering (SAXS/WAXS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and dynamic mechanical analysis (DMA). It was revealed that the tensile strength improved dramatically with increasing ND content in the PVA matrix, suggesting a strong interaction between the NDs and the PVA. SEM, TEM, and SAXS showed that NDs were present in the form of agglomerates with an average size of ~60 nm with primary particles of diameter ~5 nm. These results showed that NDs could act as a good nanofiller for PVA in terms of improving its stability and mechanical properties.

scholarly journals Green Synthesized Silver Nanoparticles Immobilized on Activated Carbon Nanoparticles: Antibacterial Activity Enhancement Study and Its Application on Textiles Fabrics

Molecules ◽  
2021 ◽  
Vol 26 (13) ◽  
pp. 3790
Author(s):  
Pratama Jujur Wibawa ◽  
Muhammad Nur ◽  
Mukhammad Asy’ari ◽  
Wijanarka Wijanarka ◽  
Heru Susanto ◽  
...  
Keyword(s):  
Silver Nanoparticles ◽  
Antibacterial Activity ◽  
Activated Carbon ◽  
Aloe Vera ◽  
Particle Size Analysis ◽  
Size Analysis ◽  
E Coli ◽  
Transmission Electron ◽  
Average Size ◽  
Green Synthesized Silver Nanoparticles

This research aimed to enhance the antibacterial activity of silver nanoparticles (AgNPs) synthesized from silver nitrate (AgNO3) using aloe vera extract. It was performed by means of incorporating AgNPs on an activated carbon nanoparticle (ACNPs) under ultrasonic agitation (40 kHz, 2 × 50 watt) for 30 min in an aqueous colloidal medium. The successful AgNPs synthesis was clarified with both Ultraviolet-Visible (UV-Vis) and Fourier Transform Infrared (FTIR) spectrophotometers. The successful AgNPs–ACNPs incorporation and its particle size analysis was performed using Transmission Electron Microscope (TEM). The brown color suspension generation and UV-Vis’s spectra maximum wavelength at around 480 nm confirmed the existence of AgNPs. The particle sizes of the produced AgNPs were about 5 to 10 nm in the majority number, which collectively surrounded the aloe vera extract secondary metabolites formed core-shell like nanostructure of 8.20 ± 2.05 nm in average size, while ACNPs themselves were about 20.10 ± 1.52 nm in average size formed particles cluster, and 48.00 ± 8.37 nm in average size as stacking of other particles. The antibacterial activity of the synthesized AgNPs and AgNPs-immobilized ACNPs was 57.58% and 63.64%, respectively (for E. coli); 61.25%, and 93.49%, respectively (for S. aureus). In addition, when the AgNPs-immobilized ACNPs material was coated on the cotton and polyester fabrics, the antibacterial activity of the materials changed, becoming 19.23% (cotton; E. coli), 31.73% (polyester; E. coli), 13.36% (cotton; S. aureus), 21.15% (polyester; S. aureus).

A New Method for Preparing Ge Nano-Crystallites Embedded in SiNY Matrices

1994 ◽  
Vol 358 ◽  
Author(s):  
Kunji Chen ◽  
Xuexuan Qu ◽  
Xinfan Huang ◽  
Zhifeng Li ◽  
Duan Feng
Keyword(s):  
Laser Annealing ◽  
Hydrogen Plasma ◽  
New Method ◽  
Transmission Electron ◽  
Scattering Spectra ◽  
Ion Laser ◽  
New Type ◽  
Raman Scattering Spectra ◽  
Average Size ◽  
20 Nm

ABSTRACTWe report a new method for synthesizing Ge nano-crystallites embedded in SiNy film matrices. On the basis of the effect of the reactant precursors and preferential chemical bonding of Si-N and Ge-Ge, thin films with Ge clusters embedded in SiNy matrices have been prepared in the PECVD system with reactant gases of SiH4, GeH4 and NH3 mixed in the hydrogen plasma. The as-deposited films were then crystallized by Ar ion laser annealing or thermal annealing technique to form nanometer-sized Ge crystallites.The composition and microstructures of these new type of sample were characterized by infrared absorption spectra, transmission electron microscopy, X-ray diffraction and Raman scattering spectra. The results indicated that the average size of Ge crystallites was estimated to be 2-20 nm depending on the deposition and annealing parameters and can be controlled by a designed manner.

Structure and Optical Properties of ZnO and ZnO2 Nanoparticles

2019 ◽  
Vol 56 ◽  
pp. 49-62 ◽  
Author(s):  
Javier Eliel Morales-Mendoza ◽  
Francisco Paraguay-Delgado ◽  
J.A. Duarte Moller ◽  
Guillermo Herrera-Pérez ◽  
Nicolaza Pariona
Keyword(s):  
Heat Treatment ◽  
Band Edge Emission ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Transmission Electron ◽  
Colloidal Method ◽  
Zinc Peroxide ◽  
Average Size ◽  
Thermal Stability Of ◽  
Raman And Ir Spectroscopy

Zinc oxide (ZnO) and Zinc peroxide (ZnO2) nanoparticles were synthesized by colloidal method at low temperature. The thermal stability of ZnO2was studied by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and X-Ray diffraction (XRD). The crystalline structure and phase change from ZnO2to ZnO by heat treatment was studied in detail. Morphology and particle size was examined using Transmission Electron Microscopy (TEM), for as synthesized ZnO and ZnO2the shape of particles were cuasi-spherical for both materials with average size of 10±2.2 nm and 2.5±0.4 nm, respectively; The crystal size for ZnO obtained by heat treatment was 8±2.2 nm. Electron density contours show the chemical bond type ionic and covalent for ZnO and ZnO2. The vibrational properties were analyzed by Raman and IR spectroscopy. Band gap values were obtained from ultraviolet-visible (UV-Vis) absorbance spectrum. Photoluminescence (PL) spectrum for ZnO shows two emission edges located at 445 and 492 nm and in the case of ZnO2presents one edge at 364 nm originated from the band edge emission. The optical spectra present a hypsochromic shift, compared with some reported in the literature.

Sintering and Dielectric Properties of Ba(Mg1/3Ta2/3)O3 Particle Prepared by Spray Pyrolysis

2008 ◽  
Vol 388 ◽  
pp. 245-248 ◽  
Author(s):  
Hiroki Yamada ◽  
Takashi Okawa ◽  
Takashi Ogihara
Keyword(s):  
Electron Microscopy ◽  
Spray Pyrolysis ◽  
Ultrasonic Spray Pyrolysis ◽  
Nano Particles ◽  
Ultrasonic Spray ◽  
Transmission Electron ◽  
Powder Particles ◽  
Average Size ◽  
Micrometer Size ◽  
20 Nm

Ba(Mg1/3Ta2/3)O3 (BMT) powders were successfully prepared by ultrasonic spray pyrolysis from an aqueous solution of Ba, Mg and Ta. The particles characteristics of BMT nano-sized powders were studied by scanning electron microscopy (SEM) and X-ray diffraction (XRD). As-prepared powder particles had a sub-micrometer size with a narrow distribution. Transmission electron microscopy (TEM) observation revealed that the average size of the BMT nano-particles was around 20 nm, and that these particles were aggregated. The dielectric constant (r) of 23.2 and the Q・f of 98,300 were obtained at 1550°C by a spray pyrolysis.

Nanocrystallization of gas atomized Cu47Ti33Zr11Ni8Si1 metallic glass

2006 ◽  
Vol 21 (3) ◽  
pp. 597-607 ◽  
Author(s):  
S. Venkataraman ◽  
S. Scudino ◽  
J. Eckert ◽  
T. Gemming ◽  
C. Mickel ◽  
...  
Keyword(s):  
Metallic Glass ◽  
Primary Crystallization ◽  
Nanocrystalline Phase ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Transmission Electron ◽  
High Resolution Tem ◽  
20 Nm ◽  
Annealing Experiments

Cu47Ti33Zr11Ni8Si1 metallic glass powder was prepared by gas atomization. Decomposition in the amorphous alloy and primary crystallization has been studied by differential scanning calorimetry (DSC), x-ray diffraction (XRD), and transmission electron microscopy (TEM). The glassy powder exhibits a broad DSC exotherm prior to bulk crystallization. Controlled annealing experiments reveal that this exotherm corresponds to a combination of structural relaxation and nanocrystallization. A uniform featureless amorphous contrast is observed in the TEM prior to the detection of nanocrystals of 4–6 nm in size. High-resolution TEM studies indicate that this nanocrystalline phase has a close crystallographic relationship with the γ–CuTi phase having a tetragonal structure. The product of the main crystallization event is also nanocrystalline, hexagonal Cu51Zr14, having dimensions of 20 nm. However, there is no evidence for possible amorphous phase separation prior to the nanocrystallization events.

Microstructure and interdiffusion behaviour of β-FeSi2 flat islands grown on Si(111) surfaces

2013 ◽  
Vol 46 (4) ◽  
pp. 1076-1080
Author(s):  
Sung-Pyo Cho ◽  
Yoshiaki Nakamura ◽  
Jun Yamasaki ◽  
Eiji Okunishi ◽  
Masakazu Ichikawa ◽  
...  
Keyword(s):  
Scanning Transmission Electron Microscopy ◽  
Single Phase ◽  
Spherical Aberration ◽  
Dark Field ◽  
Transmission Electron ◽  
Scanning Transmission ◽  
Annular Dark Field ◽  
Abrupt Interface ◽  
Average Size ◽  
20 Nm

β-FeSi2 flat islands have been fabricated on ultra-thin oxidized Si(111) surfaces by Fe deposition on Si nanodots. The microstructure and interdiffusion behaviour of the β-FeSi2/Si(111) system at the atomic level were studied by using spherical aberration-corrected high-angle annular dark-field scanning transmission electron microscopy and energy dispersive X-ray spectroscopy. The formed β-FeSi2 flat islands had a disc shape with an average size of 30–150 nm width and 10–20 nm height, and were epitaxically grown on high-quality single-phase Si with a crystallographic relationship (110)β-FeSi2/(111)Si and [001]β-FeSi2/[1\bar 10]Si. Moreover, the heterojunction between the β-FeSi2(110) flat islands and the Si(111) substrate was an atomically and chemically abrupt interface without any irregularities. It is believed that these results are caused by the use of ultra-thin SiO2 films in our fabrication method, which is likely to be beneficial particularly for fabricating practical nanoscaled devices.

Synthesis and Characterization of Polyimide/Silica Nanocomposites

2011 ◽  
Vol 311-313 ◽  
pp. 96-100
Author(s):  
Jian Li Cheng ◽  
Cun Zhou ◽  
Hao Peng ◽  
Huan Wang ◽  
Yu Sun
Keyword(s):  
Particle Size ◽  
Average Particle Size ◽  
Amic Acid ◽  
Particle Size Analysis ◽  
Size Analysis ◽  
Average Particle ◽  
Scanning Calorimetry ◽  
Silica Nanocomposites ◽  
Transmission Electron ◽  
Size Of Particles

Two kind of polyimide/silica nanocomposites which were recorded poly(amic acid)/ silica(PAA/SiO2) and SiO2in poly(amic acid) ammonium salt(PAS/SiO2) respectively, have been prepared for different methods. The size of SiO2in PAA/SiO2and PAS/SiO2are measured by Particle size analysis and the average particle size are 377nm and 53.7nm. Transmission electron microscopy(TEM) images of PAS/ SiO2confirm that the size of particles are ranged from 40 to 80nm. The stuctures of samples have been characterized by FT-IR spectra. The thermal stability of PAA/SiO2and PAS/SiO2are studied by thermogravimetric analysis (TGA) and the thermal behaviors were investigated by differential scanning calorimetry (DSC) in this paper. It is shown that PAA/SiO2have slightly better thermal properties than that of PAS/SiO2. The results obtained from Instron universal strength tester present the water-solube PAS/SiO2own the excellent mechanical prperties as same as PAA/SiO2.

scholarly journals Synthesis of BaTiO3 Nanoparticles via Hydrothermal Method

2017 ◽  
Vol 268 ◽  
pp. 172-176 ◽  
Author(s):  
Nurul Norfarina Hasbullah ◽  
Oon Jew Lee ◽  
Josephine Liew Ying Chyi ◽  
Soo Kien Chen ◽  
Zainal Abidin Talib
Keyword(s):  
Electron Microscope ◽  
Hydrothermal Method ◽  
Transmission Electron Microscope ◽  
Hydrothermal Process ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Transmission Electron ◽  
Average Size ◽  
Tga And Dsc

In this work, BaTiO3 nanoparticles were synthesized through hydrothermal method. The powder obtained from the hydrothermal process (as-synthesized powder) was calcined at 1000 °C. The phase formation and morphology of the as-synthesized and calcined powders were studied using X-ray diffraction (XRD), thermogravimetric (TGA) and differential scanning calorimetry (DSC) analyzer, and transmission electron microscope (TEM). The XRD data showed that the as-synthesized powder is partially amorphous. Upon calcining the powder at 1000 °C, highly crystalline BaTiO3 with tetragonal structure was obtained. As shown by TGA and DSC analysis, the precursor powder was completely transformed into BaTiO3 at 1000 °C. The presence of BaCO3 as an impurity phase in the powder is due to the lack of Ba2+ / Ti3+/4+. Transmission electron microscope images showed that the particle size of the as-synthesized powder increased after calcination due to crystal growth. In addition, nanocubes with the average size of around 11.66 nm were obtained as a result of the calcination compared to the ellipsoid like particles of the as-synthesized powder.

Alloy Effects And Extended Solubilities In Binary Mixtures Of Nanometer-Sized Fe-Cu Crystals

1991 ◽  
Vol 238 ◽  
Author(s):  
J. Eckert ◽  
R. Birringer ◽  
J. C. Holzer ◽  
C. E. Krill ◽  
W. L. Johnson
Keyword(s):  
Binary Mixtures ◽  
Phase Region ◽  
Alloy Formation ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Two Phase ◽  
Transmission Electron ◽  
Thermodynamic Conditions ◽  
20 Nm

ABSTRACTBinary mixtures of Fe-Cu powders in the range of 10–95 at.% Fe have been prepared by mechanical alloying and investigated by x-ray diffraction, differential scanning calorimetry (DSC), and transmission electron microscopy (TEM). The final grain sizes of the powders vary between 6 and 20 nm, and depend on the composition of the material. Indications for the formation of single-phase alloys with up to 60 at.% Fe in Cu and 20 at.% Cu in Fe have been found although the Fe-Cu system exhibits only vanishingly small solid solubilities under equilibrium conditions. Between 60 at.% and 80 at.% Fe a two-phase region of fee and bec solid solutions exists. Alloy formation is discussed with respect to the thermodynamic conditions of the material. The influence of the large grain boundary fraction, as well as the role of internal strains and stored enthalpies introduced by ball milling, is critically assessed.

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