scholarly journals Phase analysis and corrosion behavior of brazing Cu/Al dissimilar metal joint with BAl88Si filler metal

2021 ◽  
Vol 10 (1) ◽  
pp. 1318-1328
Author(s):  
Hua Yu ◽  
Liangliang Zhang ◽  
Shuai Li ◽  
Fangfang Cai ◽  
Yunpeng Li ◽  
...  

Abstract To meet the requirements of automatic production, a new type of green BAl88Si cored solder was developed. The lap brazing experiments were carried out with copper and aluminum as brazing substrates. The microstructure, phase composition, and corrosion behavior of solder joint interface were studied by field emission scanning electron microscopy, energy dispersive spectroscopy, transmission electron microscopy, electron backscattering diffraction, tensile testing machine, and electrochemical workstation. The results show that the brazing joint of Cu/BAl88Si/Al is metallurgical bonding, and the brazing joint of Cu/BAl88Si/Al is composed of Cu9Al4, CuAl2, a-Al, (CuAl2 + a-Al + Si) ternary eutectic. In addition, there is no obvious preference for each grain in the brazing joint, and there are S texture {123}<634>, Copper texture {112}<111>, and Brass texture {110}<112>. The interface of Cu9Al4/CuAl2 is a non-coherent crystal plane and does not have good lattice matching. The average particle size of CuAl2 is 11.95 µm and that of Al is 28.3 µm. However, the kernel average misorientation (KAM) value at the brazed joint interface is obviously higher than that at the brazed joint interface copper, so the defect density at the brazed joint interface aluminum is higher than that at the brazed joint interface copper. At the same time, due to poor corrosion resistance at the interface on the aluminum side of the brazed joint, serious corrosion spots and corrosion cracks occur at the same time, which leads to the shear performance of the brazed joint decreasing by about 75% after salt spray test for 240 h.

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.


1997 ◽  
Vol 496 ◽  
Author(s):  
David J. Derwin ◽  
Kim Kinoshita ◽  
Tri D. Tran ◽  
Peter Zaleski

AbstractSeveral types of carbonaceous materials from Superior Graphite Co. were investigated for lithium ion intercalation. These commercially available cokes, graphitized cokes and graphites have a wide range of physical and chemical properties. The coke materials were investigated in propylene carbonate based electrolytes and the graphitic materials were studied in ethylene carbonate / dimethyl solutions to prevent exfoliation. The reversible capacities of disordered cokes are below 230 mAh / g and those for many highly ordered synthetic (artificial) and natural graphites approached 372 mAh / g (LiC6). The irreversible capacity losses vary between 15 to as much as 200 % of reversible capacities for various types of carbon. Heat treated cokes with the average particle size of 10 microns showed marked improvements in reversible capacity for lithium intercalation. The electrochemical characteristics are correlated with data obtained from scanning electron microscopy (SEM), high resolution transmission electron microscopy (TAM), X - ray diffraction (XRD) and BET surface area analysis. The electrochemical performance, availability, cost and manufacturability of these commercial carbons will be discussed.


2021 ◽  
Vol 6 (1) ◽  
pp. 32-36
Author(s):  
Anh Quoc Le ◽  
Van Phu Dang ◽  
Ngoc Duy Nguyen ◽  
Kim Lan Nguyen Thi ◽  
Kim Lang Vo Thi ◽  
...  

Silver nanoparticles (AgNPs) doped in the zeolite framework (AgNPs/Z) were successfully synthesized by γ-irradiation in ethanol solution of silver ion-zeolite (Ag+/Z) prepared by ion exchange reaction between silver nitrate (AgNO3) and zeolite 4A. The effects of the Ag+ concentration and irradiation dose on the formation of AgNPs/Z were also investigated. AgNPs/Z with the silver content of about 10,000 ppm and the average particle size of AgNPs of about 27 nm was characterized by ultraviolet-visible spectroscopy, powder X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM). Firstly, AgNPs/Z was added into PP resins for creation of PP-AgNPs/Z masterbatch (Ag content of ~10.000 ppm) and then PP-AgNPs/Z plastics were preapared by mixing masterbatch with PP resins. The antibacterial activity of the PP-AgNPs/Z plastics was investigated against Gram-negative bacteria Escherichia coli (E. coli). The results showed that PP-AgNPs/Z plastic contained 100 ppm of Ag possessed a high antibacterial property, namely the bactericidal effect was more than 96 % on the platic surface. In conclusion, possessing many advantages such as: vigorously antibacterial effect and good dispersion in plastic matrix, AgNPs/Z is promising to be applied as bactericidal agent for plastic industry.


2013 ◽  
Vol 66 (5) ◽  
pp. 564 ◽  
Author(s):  
Mingmei Zhang ◽  
Qian Sun ◽  
Zaoxue Yan ◽  
Junjie Jing ◽  
Wei Wei ◽  
...  

Well dispersed Pd@Ni bimetallic nanoparticles on multi-walled carbon nanotubes (Pd@Ni/MWCNT) are prepared and used as catalysts for the oxidation of benzyl alcohol. Scanning electron microscopy, transmission electron microscopy, energy-dispersive X-ray spectroscopy analysis, and X-ray diffraction were performed to characterise the synthesised catalyst. The results show a uniform dispersion of Pd@Ni nanoparticles on MWCNT with an average particle size of 4.0 nm. The as synthesised catalyst was applied to the oxidation of benzyl alcohol. A 99 % conversion of benzyl alcohol and a 98 % selectivity of benzaldehyde were achieved by using the Pd@Ni/MWCNT (Pd: 0.2 mmol) catalyst with water as a solvent and H2O2 as oxidant at 80°C. The catalytic activity of Pd@Ni/MWCNT towards benzyl alcohol is higher than that of a Pd/MWCNT catalyst at the same Pd loadings. The catalyst can be easily separated due to its magnetic properties.


2019 ◽  
Vol 19 (11) ◽  
pp. 7487-7492 ◽  
Author(s):  
Supriya ◽  
Jayanta Kumar Basu ◽  
Sonali Sengupta

Synthesis of silver nanoparticles embedded on calcium alginate film and the catalytic property of this film in the reduction of nitrobenzene with sodium borohydride are demonstrated in this work. Natural polymer alginate acts as effective reducing and stabilizing agent in synthesis of silver nanoparticles. Effect of different parameters on the preparation of silver nanoparticles, such as, temperature, concentration of silver precursor and heating time was investigated. As-prepared silver nanoparticles were characterized by transmission electron microscopy, scanning electron microscopy, UV-Vis spectrometry, and atomic absorption spectrometry. Transmission electron microscopy analysis con-firms the formation of silver nanoparticles with particles size range of 3–19 nm and average particle size was found to be 10±4 nm. Effect of concentration of nitrobenzene and sodium borohydride, catalyst loading and temperature on the catalytic reduction of nitrobenzene was studied. Reusability of catalyst was examined in this reduction reaction and the catalyst shows good activity up to 10th run.


2010 ◽  
Vol 152-153 ◽  
pp. 81-85
Author(s):  
Xiong Wang ◽  
Yin Lin ◽  
Jin Guo Jiang

The homogeneous multiferroic BiFeO3 nanoparticles with average particle size of 85 nm have been successfully synthesized by a simple sol-gel route. The prepared sample was characterized by a variety of techniques, such as X-ray diffractometry, thermogravimetric analysis and differential thermal analysis, differential scanning calorimeter analysis, scanning electron microscopy, transmission electron microscopy and X-ray photoelectron spectroscopy. The obtained results shows that rapid sintering and subsequently quenching to room temperature are the two vital important factors for the preparation of pure BiFeO3. The magnetic phase transition (TN = 369 °C) and the ferroelectric phase transition (TC = 824.5 °C) were determined, revealing the antiferromagnetic and ferroelectric nature of the as-prepared BiFeO3 nanoparticles. The optical properties of the nanopowders were investigated. The strong band-gap absorption at 486 nm (2.55 eV) of the BiFeO3 nanoparticles may bring some novel applications.


2014 ◽  
Vol 9 (1) ◽  
pp. 155892501400900 ◽  
Author(s):  
Hui Zhang ◽  
Linlin Zhu ◽  
Runjun Sun

Cotton fibers were treated with titanium sulfate, urea and hexadecyl trimethyl ammonium bromide by low temperature hydrothermal method. The surface morphology, chemical structure, thermal stability and optical properties of cotton fibers before and after treatments were studied by scanning electron microscopy (SEM), transmission electron microscopy(TEM), Fourier transform infrared spectroscopy (FTIR), X–ray photoelectron spectroscopy (XPS), thermal gravimetric (TG) and diffuse reflectance spectrum (DRS). The properties of tensile, friction and self–cleaning capability to discolor strawberry juice stain were also measured. The results showed that titanium dioxide (TiO2) nanoparticles in anatase phase with an average particle size of 50 nm were grafted on the surfaces of cotton fibers. The crystallites of TiO2 were less than 10 nm in size. In comparison with the original cotton fibers, the thermal properties of TiO2 coated cotton fibers had almost no change. The protection against ultraviolet radiation was obtained. However, the tensile properties decreased to some extent. The coefficients of static and kinetic friction increased because of the introduction of TiO2 nanoparticles. The strawberry juice stained on cotton fibers could be discolored exposure to UV radiation.


Processes ◽  
2020 ◽  
Vol 8 (9) ◽  
pp. 1040
Author(s):  
Nurhanisah Othman ◽  
Siti Nurul Ain Md. Jamil ◽  
Mas Jaffri Masarudin ◽  
Luqman Chuah Abdullah ◽  
Rusli Daik ◽  
...  

Encapsulation of dual compounds of different characters (hydrophilic and hydrophobic) in single nanoparticles carrier could reach the site of action more accurately with the synergistic effect but it is less investigated. In our previous findings, combined-compounds encapsulation and delivery from chitosan nanoparticles were impaired by the hydrophilicity of chitosan. Therefore, hydrophobic modification on chitosan with palmitic acid was conducted in this study to provide an amphiphilic environment for better encapsulation of antioxidants; hydrophobic thymoquinone (TQ) and hydrophilic l-ascorbic acid (LAA). Palmitoyl chitosan nanoparticles (PCNPs) co-loaded with TQ and LAA (PCNP-TQ-LAA) were synthesized via the ionic gelation method. Few characterizations were conducted involving nanosizer, Fourier-transform infrared spectroscopy (FTIR), field-emission scanning electron microscopy (FESEM) and high-resolution transmission electron microscopy (HRTEM). UV–VIS spectrophotometry was used to analyze the encapsulation and release efficiency of the compounds in PCNPs. Successfully modified PCNP-TQ-LAA had an average particle size of 247.7 ± 24.0 nm, polydispersity index (PDI) of 0.348 ± 0.043 and zeta potential of 19.60 ± 1.27 mV. Encapsulation efficiency of TQ and LAA in PCNP-TQ-LAA increased to 64.9 ± 5.3% and 90.0 ± 0%, respectively. TQ and LAA in PCNP-TQ-LAA system showed zero-order release kinetics, with a release percentage of 97.5% and 36.1%, respectively. Improved preparation method, encapsulation and release efficiency in this study are anticipated to be beneficial for polymeric nanocarrier development.


2017 ◽  
Vol 31 (15) ◽  
pp. 1750118 ◽  
Author(s):  
Abdur Rauf ◽  
Syed Sohail Ahmad Shah ◽  
Sobia Allah Rakha ◽  
Munazza Gul ◽  
Ishaq Ahmad ◽  
...  

A chemical two-step approach based on solvothermal technique has been adopted to synthesize the reduced graphene oxide (rGO)/Fe2O3 hybrid materials. The rGO was prepurified by acidic treatment, followed by sensitization to attach the desired functional groups. The structural, compositional, morphological and magnetic analyzes of the prepared samples were carried out using various characterization techniques. The fabricated rGO/Fe2O3 heterostructures were confirmed by X-ray diffraction analysis and Fourier transform infrared spectroscopy. Raman spectroscopy evidenced the fabrication of multilayer graphene and scanning electron microscopy was carried out to study the morphology of the prepared samples. The average particle size of Fe2O3 nanoparticles (NPs) loaded on rGO was found to be [Formula: see text]20 nm, as was observed during transmission electron microscopy. Thermogravimetric analysis of rGO/Fe2O3 hybrid structures was performed to investigate their thermal behaviors. It was evidenced that the incorporation of Fe2O3 NPs into rGO enhanced its thermal stability. Vibrating sample magnetometry showed that ferromagnetic character was induced in rGO due to involvement of Fe2O3 NPs. The rGO/Fe2O3 hybrid structures can be considered as a competent material for fabrication of various magnetic devices.


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.


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