scholarly journals Characterization and Electrical Properties of PVA Films with Self-Assembled Chitosan-AuNPs/SWCNT-COOH Nanostructures

Materials ◽  
2020 ◽  
Vol 13 (18) ◽  
pp. 4138 ◽  
Author(s):  
Israel Ceja ◽  
Karla Josefina González-Íñiguez ◽  
Alejandra Carreón-Álvarez ◽  
Gabriel Landazuri ◽  
Arturo Barrera ◽  
...  

Nanostructured films with electrical conductivity in the semiconductor region were prepared in a polymeric matrix of poly(vinyl alcohol) (PVA) with nanostructures of chitosan-gold nanoparticles (AuNPs)/single-wall carbon nanotubes carboxylic acid functionalized (SWCNT-COOH) (chitosan-AuNPs/SWCNT-COOH) self-assembled. Dispersion light scattering (DLS) was used to determine the average particle sizes of chitosan-AuNPs, z-average particle size (Dz) and number average particle size (Dn), and the formation of crystalline domains of AuNPs was demonstrated by X-ray diffraction (XRD) patterns and observed by means of transmission electron microscopy (TEM). The electrostatic interaction was verified by Fourier transform infrared spectroscopy (FTIR). The electrical conductivity of PVA/chitosan-AuNPs/SWCNT-COOH was determined by the four-point technique and photocurrent. The calculated Dn values of the chitosan-AuNPs decreased as the concentration of gold (III) chloride trihydrate (HAuCl4·3H2O) increased: the concentrations of 0.4 and 1.3 mM were 209 and 90 nm, respectively. Average crystal size (L) and number average size (D) of the AuNPs were calculated in the range of 13 to 24 nm. Electrical conductivity of PVA/chitosan-AuNPs/SWCNT-COOH films was 3.7 × 10−5 σ/cm determined by the four-point technique and 6.5 × 10−4 σ/cm by photocurrent for the SWCNT-COOH concentration of 0.5 wt.% and HAuCl4·3H2O concentration of 0.4 mM. In this investigation, the protonation of the amine group of chitosan is fundamental to prepare PVA films with nanostructures of self-assembled chitosan-AuNPs/SWCNT-COOH.

2010 ◽  
Vol 8 (5) ◽  
pp. 1041-1046 ◽  
Author(s):  
Raúl Reza ◽  
Carlos Martínez Pérez ◽  
Claudia Rodríguez González ◽  
Humberto Romero ◽  
Perla García Casillas

AbstractIn this work, the synthesis of magnetite nanoparticles by two variant chemical coprecipitation methods that involve reflux and aging conditions was investigated. The influence of the synthesis conditions on particle size, morphology, magnetic properties and protein adsorption were studied. The synthesized magnetite nanoparticles showed a spherical shape with an average particle size directly influenced by the synthesis technique. Particles of average size 27 nm and 200 nm were obtained. When the coprecipitation method was used without reflux and aging, the smallest particles were obtained. Magnetite nanoparticles obtained from both methods exhibited a superparamagnetic behavior and their saturation magnetization was particle size dependent. Values of 67 and 78 emu g−1 were obtained for the 27 nm and 200 nm magnetite particles, respectively. The nanoparticles were coated with silica, aminosilane, and silica-aminosilane shell. The influence of the coating on protein absorption was studied using Bovine Serum Albumin (BSA) protein.


2010 ◽  
Vol 2010 ◽  
pp. 1-7 ◽  
Author(s):  
Antonio M. Brito-Silva ◽  
Luiz A. Gómez ◽  
Cid B. de Araújo ◽  
André Galembeck

Poly(vinyl-pyrrolidone) (PVP) stabilized silver nanoparticles with an average particle size ranging from 4.3 to 4.9 nm were synthesized by laser ablation in preformed colloids in methanol, acetone, ethylene glycol, and glycerin. Aqueous colloids obtained using PVP, poly(vinyl-alcohol) (PVA), and sodium citrate as stabilizing agents also lead to a good control over particle size distribution. Silver ions were reduced with sodium borohydride. The smaller average particle size and narrower dispersivity in comparison to previously reported data were ascribed to the relatively small size of the particles formed in the chemical reduction step, laser fluence, and the use of PVP, which was not previously used as the stabilizing agent in “top-down” routes. The surface plasmon resonance band maximum wavelength shifted from 398 nm in methanol to 425 nm in glycerin. This shift must be due to solvent effects since all other variables were the same.


2012 ◽  
Vol 463-464 ◽  
pp. 760-763
Author(s):  
Zhen Zhao Pei ◽  
Hong Bin Xu ◽  
Yi Zhang

Nanoparticles of Cr2O3 were successfully obtained via hydrothermal reduction of CH3OH. The oxidant and chromium source was CrO3. The process needs no stirrer or surfactant and the CrO3 concentration was 0.83mol/L. The obtained products were loosely agglomerated Cr2O3 nanoparticles with the average size of 29 to 79 nm. Influences of reactant ratios and calcination temperatures on the specific surface area and average particle size were discussed. And the morphology of nanoparticles was investigated by use of field-emission scanning electron microscope.


2015 ◽  
Vol 1107 ◽  
pp. 301-307 ◽  
Author(s):  
Salahudeen A. Gene ◽  
Elias B. Saion ◽  
Abdul Halim Shaari ◽  
Mazliana A. Kamarudeen ◽  
Naif Mohammed Al-Hada

The fabrication of nanospinel zinc chromite (ZnCr2O4) crystals by the means of thermal treatment method from an aqueous solution containing metal nitrates, polyvinyl pyrrolidone (PVP), and deionized water was described in this study. The samples were calcined at various temperatures ranging from 773 to 973 K for the decomposition of the organic compounds and crystallization of the nanocrystals. PVP was used as capping agent to control the agglomeration of the particles. The characterization studies of the fabricated samples were carried out by X-ray diffraction spectroscopy (XRD), transmission electron microscopy (TEM), energy dispersed X-ray spectroscopy (EDX) and electron spin resonance spectroscopy (ESR). The corresponding peaks of Zn, Cr and O were observed in the EDX spectrum of the sample which confirms the formation of ZnCr2O4. The XRD patterns also confirmed the formation of the single faced nanocrystallines of spinel ZnCr2O4 with a face-centered cubic structure. The average particle size of the synthesized crystals was also determined from the XRD patterns using the Scherers formula which shows that the crystallite sizes increases with increase in calcination temperature and was in good agreement with the TEM images which shows cubical ZnCr2O4 nanocrystals with uniform morphology and particle size distributions. The ESR spectra confirmed the existence of unpaired electron in the fabricated samples and the increase in g-factor and decreases in resonant magnetic field (Hr) were observed as the calcination temperature increases.


2016 ◽  
Vol 30 (18) ◽  
pp. 1650247 ◽  
Author(s):  
Mahdi Ghasemifard ◽  
Misagh Ghamari ◽  
Meysam Iziy

TiO2-(Ti[Formula: see text]Si[Formula: see text]O2 nanopowders (TS-NPs) with average particle size around 90 nm were successfully synthesized by controlled auto-combustion method by using citric acid/nitric acid (AC:NA) and urea/metal cation (U:MC). The structure of powders was studied based on their X-ray diffraction (XRD) patterns. The XRD of TS-NPs shows that rutile and anatase are the main phases of TS-NPs for AC:NA and U:MC, respectively. Particle size and histogram of nanopowders were characterized by transmission electron microscopy (TEM) and dynamic light scattering (DLS). Optical properties of TS-NPs were calculated by Fourier transform infrared spectroscopy (FTIR) and Kramers–Kroning (KK) relation. Plasma frequencies of TS-NPs obtained from energy loss functions depend on fuels as a result of changes in crystal structure, particle size distribution, and morphology.


2005 ◽  
Vol 475-479 ◽  
pp. 1763-1766 ◽  
Author(s):  
Yan Wang ◽  
Yang Liu ◽  
Ju Sheng Ma ◽  
Zhaowen Dong ◽  
Mingli Yin

Fine Au powders with spherical morphology and good dispersivity were produced. The average particle size is 1~2m. The influences of constituents on the rheology of organic vehicles were investigated by orthogonal design method. Consequently, the compatible Au thick film pastes for LTCC substrate have been prepared. SEM was carried out to study the sintering behaviors and microstructures of the buried pastes with LTCC substrate. These pastes have high electrical conductivity (less than 3m/sq.), reliable wire bond strength (greater than 9 grams, 25m Au wire) and fine line printability (as small as 80m). The via filling technology was also discussed in this paper.


2009 ◽  
Vol 421-422 ◽  
pp. 269-272
Author(s):  
Takashi Kubo ◽  
Masayuki Hogiri ◽  
Hiroshi Kagata ◽  
Atsushi Nakahira

Nano-sized BaTiO3 powders with narrow size distribution and the high tetragonality were attempted to synthesize by the rotary-hydrothermal process in water system, using two kinds of commercial anatase-type TiO2 (ST21/ST01) with different particle size and Ba(OH)2. The rotary-hydrothermal syntheses were done with the rotary-speed of 20 revolutions per minute at 523 K for 24 h. Highly- and mono-dispersed BaTiO3 powders were successfully synthesized by applying the rotary-hydrothermal process. For rotary-hydrothermal synthesis, it was found that the average size, tetragonality, and quality of the BaTiO3 particle strongly depended on the particle size of the starting material. In the case of using ST01 as a starting material, BaTiO3 nano-powders mainly composed of coarse-faceted particles (average particle size = ca.100 nm) with the tetragonal phase and very little lattice defects were successfully synthesized.


Drug Research ◽  
2017 ◽  
Vol 67 (05) ◽  
pp. 266-270 ◽  
Author(s):  
Ebrahim Izadi ◽  
Ali Rasooli ◽  
Abolfazl Akbarzadeh ◽  
Soodabeh Davaran

AbstractThrough the present study, an eco-friendly method was used to synthesize the gold nanoparticles (GNPs) by using the sodium citrate and extract of the soybean seed as reducing the agents at PH 3. X-Ray diffraction (XRD) method was used to evaluate the crystal structure of as-synthesized NPs and it’s revealed that this method leads to well crystallized GNPs. In order to determine the particle size and their distribution, field emission scanning microscopy (FE-SEM) and dynamic light scattering (DLS) were used. The results showed that, the average particle size distribution of synthesized GNPs in solutions containing of the soybean extract and 1% citrate at PH 3 is about 109.6 and 140.9 nm, respectively. Also, we find that the average size of GNPs is 40 and 33 nm from solutions of citrate and soybean extract, respectively. It was concluded that using the extract of soybean seeds as reducing agent can lead to GNPs with small size and narrow size distribution.


2021 ◽  
Vol 27 (1) ◽  
pp. 119-124
Author(s):  
Wenzheng XU ◽  
Hao LI ◽  
Xin LIANG ◽  
Jie WANG ◽  
Jinyu PENG ◽  
...  

In this paper, the ultrafine β-hexanitrohexaazaisowurtzitane (β – CL – 20) particles were prepared by spray drying method. The CL – 20 samples were characterized by scanning electron microscope (SEM), particle size analyzer, X-ray diffraction (XRD), and Differential Scanning Calorimeter (DSC). Furthermore, the safety properties of samples under impact and thermal stimulus were tested and analyzed. The results of SEM showed that the average particle size of ultrafine CL – 20 particles with a narrow particle size distribution, were about 320 nm, and the shape was elliptical. The XRD patterns indicated that the polymorphic phase of ultrafine particles was mainly β-type. Compared with that of raw CL – 20, the impact sensitivity of the ultrafine CL – 20 had been decreased significantly, for the drop height (H50) was increased from 13.0 to 33.5 cm. The critical explosion temperature of the ultrafine CL – 20 decreased from 232.16 ℃ to 227.93 ℃, indicating that the thermal stability of the ultrafine CL – 20 is lower than that of raw CL – 20.


2021 ◽  
Vol 1 ◽  
pp. 58-66
Author(s):  
A.A. Vasilev ◽  
◽  
E.L. Dzidziguri ◽  
M.N. Efimov ◽  
D.G. Muratov ◽  
...  

A method for the synthesis of nanoparticles of the Cu-Fe bimetallic system with limited mutual solubility of the components is proposed. The synthesis method consists of a one-stage process of IR pyrolysis of precursors in the form of films obtained from a joint solution of polyacrylonitrile and hydrates-nitrates of iron and copper. The effect of the synthesis temperature on the structure formation of the nanocomposites and the phase composition of bimetallic Cu-Fe nanoparticles dispersed in the carbon matrix was studied. The analysis showed a simultaneous presence of Fe and Cu phases in nanocomposites, presumably with a low solubility of the components. The average particle size is 14-17 nm and changes insignificantly with an increase in the synthesis temperature from 400 to 700°C. An increase in the synthesis temperature to 800°C led to a broadening of the particle size distribution and the increase in the average size. The formation of complex carbon nanostructures on Cu-Fe nanoparticles is found.


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