scholarly journals A Study of Fabricating Nano-W Colloid by Discharge Energy Enhancement of the micro-EDM System

Author(s):  
Chaur-Yang Chang ◽  
Kuo-Hsiung Tseng ◽  
Jui-Tsun Chang ◽  
Meng-Yun Chung ◽  
Zih-Yuan Lin

Abstract This study enhanced the discharge energy of an existing micro-electric discharge machining (EDM) system to provide the system with the ability to prepare nano-tungsten (nano-W) colloid. The energy- enhanced EDM system, referred to as the upgraded-micro-EDM system, enables spark discharge using tungsten wires immersed in deionized water to produce nano-W colloids. Compared with the chemical preparation method, the processing environment for preparing colloids will not have nanoparticle escape in this study. Among the nano-W colloids prepared using the upgraded-micro-EDM system and an industrial EDM system, the colloid prepared by the upgraded-micro-EDM system exhibited more favorable absorbance, suspensibility, and particle size. The colloid prepared by the upgraded-micro-EDM system with the pulse on time and off time of 10–10 µs had an absorbance of 0.277 at the wavelength of 315 nm, ζ potential of −64.9 mV, and an average particle size of 164.9 nm. Transmission electron microscope imaging revealed the minimum particle size of approximately 11 nm, and the X-ray diffractometer spectrum verified that the colloid contained only \({\text{W}}_{2.00}\) and W nanoparticles. Relative to industrial EDM applications for nano-W colloid preparation, the upgraded system boasts lower costs and smaller size, and produces nano-W colloid with superior performance. These advantages contribute to the competitiveness of electrical spark discharge method in the preparation of high-quality nano-W colloids.

2012 ◽  
Vol 476-478 ◽  
pp. 1138-1141
Author(s):  
Zhi Qiang Wei ◽  
Qiang Wei ◽  
Li Gang Liu ◽  
Hua Yang ◽  
Xiao Juan Wu

Ag nanoparticles were successfully synthesized by hydrothermal method under the polyol system combined with traces of sodium chloride, Silver nitrate(AgNO3) and polyvinylpyrrolidone (PVP) acted as the silver source and dispersant respectively. The samples by this process were characterized via X-ray powder diffraction (XRD), Brunauer–Emmett–Teller (BET) adsorption equation, transmission electron microscopy (TEM) and the corresponding selected area electron diffraction (SAED) to determine the chemical composition, particle size, crystal structure and morphology. The experiment results indicate that the crystal structure of the samples is face centered cubic (FCC) structure as same as the bulk materials, The specific surface area is 24 m2/g, the particle size distribution ranging from10 to 50 nm, with an average particle size about 26 nm obtained by TEM and confirmed by XRD and BET results.


2011 ◽  
Vol 415-417 ◽  
pp. 617-620 ◽  
Author(s):  
Yan Su ◽  
Ying Yun Lin ◽  
Yu Li Fu ◽  
Fan Qian ◽  
Xiu Pei Yang ◽  
...  

Water-soluble gold nanoparticles (AuNPs) were prepared using 2-mercapto-4-methyl-5- thiazoleacetic acid (MMTA) as a stabilizing agent and sodium borohydride (NaBH4) as a reducing agent. The AuNPs product was analyzed by transmission electron microscopy (TEM), UV-vis absorption spectroscopy and Fourier transform infrared spectroscopy (FTIR). The TEM image shows that the particles were well-dispersed and their average particle size is about 5 nm. The UV-vis absorption and FTIR spectra confirm that the MMTA-AuNPs was stabilized by the carboxylate ions present on the surface of the AuNPs.


2016 ◽  
Vol 709 ◽  
pp. 66-69
Author(s):  
Jeyashelly Andas ◽  
Rahmah Atikah Rosdi ◽  
Nur Izzati Mohd Anuar

A series of Fe-Co nanoparticles were synthesized via sol-gel route at acidic, neutral and basic condition using rice husk as the silica source. The synthesized nanomaterials were designated as Fe-Co3, Fe-Co7 and Fe-Co9 and characterized by Fourier Transform Infrared (FTIR), Transmission Electron Microscope (TEM) and particle size analyzer. The great effect of pH was clearly evidenced from the shifting in the siloxane bond in the FTIR spectrum. TEM investigation confirmed the existence of discrete and almost sphere like nanoparticles. The particle size decreased with an increase in the pH, registering the smallest average particle size at pH 9. In brief, this study promises a fast, rapid and promising method for the conversion of silica rice husk into nanoscale bimetallic materials.


2017 ◽  
Vol 263 ◽  
pp. 165-169
Author(s):  
Silvia Chowdhury ◽  
Faridah Yusof ◽  
Nadzril Sulaiman ◽  
Mohammad Omer Faruck

In this article, we have studied the process of silver nanoparticles (AgNPs) aggregation and to stop aggregation 0.3% Polyvinylpyrrolidone (PVP) was used. Aggregation study carried out via UV-vis spectroscopy and it is reported that the absorption spectrum of spherical silver nanoparticles were found a maximum peak at 420 nm wavelength. Furthermore, Transmission Electron Microscopy (TEM) were used to characterized the size and shape of AgNPs, where the average particle size is around 10 to 25 nm in diameter and the AgNPs shape is spherical. Next, Dynamic Light Scattering (DLS) were used, owing to observed size distribution and self-correlation of AgNPs.


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.


2016 ◽  
Vol 17 (1) ◽  
pp. 1-3 ◽  
Author(s):  
Sujan Dhungana ◽  
Bhoj Raj Paudel ◽  
Surendra K. Gautam

In this work, we report the ZnTe semiconductor nanoparticles (NPs) prepared by aqueous chemical precipitation method using the tellurium precursor solution with different zinc compounds. Three batches of ZnTe NPs were synthesized to study the effect of dilution on the size and phase purity of ZnTe. The influence of source compounds and concentrations of the size and structure of NPs were studied. ZnTe NPs have great applications as field-effect transistors and photodetectors. The existing controversy regarding the crystalline structure of ZnTe NPs, whether it is cubic or hexagonal, has been resolved using X-ray Diffraction (XRD) data. The ZnTe NPs possess cubic structure, which is also confirmed by Electron Diffraction (ED) pattern. The average particle size determined from XRD data with the help of Debye-Scherrer equation is about 6 nm. The particle size can be further verified by Transmission Electron Microscopy (TEM) studies.  


2020 ◽  
Vol 20 (11) ◽  
pp. 6723-6731
Author(s):  
Mi Choi ◽  
Cheong-Soo Hwang

Colloidal ZnS:Mn nanocrystals (NCs) were synthesized in water by capping the NC surface with conventional amino acids: L-cysteine (Cys) and L-serine (Ser) molecules, which have very similar structures but different terminal functional groups. The optical properties were investigated by using UV-Visible and photoluminescence (PL) spectroscopy. The PL spectra for both ZnS:Mn-Cys and ZnS:Mn-Ser NCs showed broad emission peaks at 590 nm. The measured average particle size from the high-resolution transmission electron microscopy (HR-TEM) images were 4.38 nm (ZnS:Mn-Cys) and 5.57 nm (ZnS:Mn-Ser), which were also supported by Debye-Scherrer calculations. In addition, the surface charge of the NCs in aqueous solutions were measured using zeta-particle size analyzer spectroscopy, which showed formation of negatively charged surface for the ZnS:Mn-Cys (−43.93 mV) and ZnS:Mn-Ser (−8.21 mV) NCs in water. In this present study those negatively charged NCs were applied as photosensors for the detection of specific divalent transition metal cations in aqueous solution at the same condition. Consequently, the ZnS:Mn-Cys and ZnS:Mn-Ser NCs showed totally different photosensor activities upon the addition of first-row divalent transition metal ions. The former NCs showed luminescence quenching for most added metal ions except for Zn (II) ions; whereas the latter NCs showed exclusive quenching effect for Cu (II) ions at the same conditions. These results suggested that those NCs can be applied as Zn2+ and Cu2+ ion sensors in water.


2011 ◽  
Vol 311-313 ◽  
pp. 96-100
Author(s):  
Jian Li Cheng ◽  
Cun Zhou ◽  
Hao Peng ◽  
Huan Wang ◽  
Yu Sun

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.


Author(s):  
B. Graham ◽  
R.F. Klie

In the hope of optimizing the Fischer-Tropsch mechanism to produce cleaner ethanol, the catalyst- promoter interaction between rhodium and manganese was examined by transmission electron microscopy. Three samples were analyzed on a carbon nanotube (CNT) substrate with 3 wt% rhodium (3%Rh/CNT), 1% manganese with 3 wt% rhodium (1%Mn/3% Rh/CNT), and 2% manganese with 3 wt% rhodium (2% Mn/3% Rh/CNT). The average particle size were found to be (1.9 ± 0.6) nm, (2.1 ± 0.5) nm, and (3.2 ± 0.6) nm, respectively. An increase in particle size indicates that the rhodium and manganese are interacting. The lattice parameter for rhodium were also determined to be (4.1 ± 0.1) Å, (4.2 ± 0.1) Å, and (3.8 ± 0.1) Å, respectively. The decrease in lattice parameter in the 2%Mn/3%Rh/CNT sample was most likely due to a change in the crystal structure of the rhodium particles as a result of the interaction between the manganese and rhodium.


Materials ◽  
2018 ◽  
Vol 11 (8) ◽  
pp. 1285 ◽  
Author(s):  
Andrei Trofimuk ◽  
Diana Muravijova ◽  
Demid Kirilenko ◽  
Aleksandr Shvidchenko

Detonation nanodiamond is a commercially available synthetic diamond that is obtained from the carbon of explosives. It is known that the average particle size of detonation nanodiamond is 4–6 nm. However, it is possible to separate smaller particles. Here we suggest a new approach for the effective separation of detonation nanodiamond particles by centrifugation of a “hydrosol/glycerol” system. The method allows for the production of the detonation nanodiamond hydrosol with a very sharp distribution in size, where more than 85% of particles have a size ranging 1–4 nm. The result is supported by transmission electron microscopy, atomic force microscopy, and dynamic light scattering.


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