Microstructure and Tensile Properties of As-Cast Mg-5Sn-4Cu Alloy

2014 ◽  
Vol 788 ◽  
pp. 78-81
Author(s):  
Xu Dong Wang ◽  
Zheng Lu ◽  
Zhao Hui Feng ◽  
Xian Feng Zhang ◽  
Zhi Feng Ma ◽  
...  

The microstructure and tensile properties of permanent-mould cast Mg-5wt%Sn-4wt%Cu alloy was investigated by transmission electron microscopy (TEM), scanning electron microscopy (SEM) and tensile test in this paper. The result indicated that the microstructures of the as-cast samples consist of 30-40 μm size primary solidification phase, primary dendrite Mg2(Cu,Sn) which is a network-like interdendritic eutectic intermetallic compounds along grain boundaries and particle like Mg2(Sn,Cu) phases. The Mg-5Sn-4Cu alloy exhibit maximum ultimate tensile strength and yield strength, and the values are 142 MPa and 91 MPa at room temperature. This improved mechanical property is mainly ascribed to the formation of network-like secondary phases of primary dendrite Mg2(Cu,Sn).

Author(s):  
A.J. Tousimis ◽  
T.R. Padden

The size, shape and surface morphology of human erythrocytes (RBC) were examined by scanning electron microscopy (SEM), of the fixed material directly and by transmission electron microscopy (TEM) of surface replicas to compare the relative merits of these two observational procedures for this type specimen.A sample of human blood was fixed in glutaraldehyde and washed in distilled water by centrifugation. The washed RBC's were spread on freshly cleaved mica and on aluminum coated microscope slides and then air dried at room temperature. The SEM specimens were rotary coated with 150Å of 60:40- gold:palladium alloy in a vacuum evaporator using a new combination spinning and tilting device. The TEM specimens were preshadowed with platinum and then rotary coated with carbon in the same device. After stripping the RBC-Pt-C composite film, the RBC's were dissolved in 2.5N HNO3 followed by 0.2N NaOH leaving the preshadowed surface replicas showing positive topography.


2021 ◽  
Vol 1026 ◽  
pp. 84-92
Author(s):  
Tao Qian Cheng ◽  
Zhi Hui Li

Al-Zn-Mg-Cu alloy have been widely used in aerospace industry. However, there is still a lack of research on thermal stability of Al-Zn-Mg-Cu alloy products. In the present work, an Al-Zn-Mg-Cu alloy with T79 and T74 states was placed in the corresponding environment for thermal exposure experiments. Performance was measured by tensile strength, hardness and electrical conductivity. In this paper, precipitation observation was analyzed by transmission electron microscopy (TEM) and high-resolution transmission electron microscopy (HREM). The precipitations of T79 state alloy were GPⅡ zone, η' phase and η phase while the ultimate tensile strength, hardness and electrical conductivity were 571MPa, 188.2HV and 22.2MS×m-1, respectively. The mechanical property of T79 state alloy decreased to 530MPa and 168.5HV after thermal exposure. The diameter of precipitate increased and the precipitations become η' and η phase at the same time. During the entire thermal exposure, T74 state alloy had the same mechanical property trend as T79 state alloy. The precipitate diameter also increased while the types of precipitate did not change under thermal exposure. The size of precipitates affected the choice of dislocation passing through the particles to affect the mechanical properties.


2014 ◽  
Vol 979 ◽  
pp. 184-187
Author(s):  
Weerachon Phoohinkong ◽  
Thitinat Sukonket ◽  
Udomsak Kitthawee

Zinc sulfide (ZnS) nanostructures are important materials for many technologies such as sensors, infrared windows, transistors, LED displays, and solar cells. However, many methods of synthesizing ZnS nanostructures are complex and require expensive equipment. In this study, a liquid-solid chemical reaction without surfactant was used to synthesize ZnS at room temperature. In addition, commercial grade zinc oxide (ZnO) particles were used as a precursor. The effect of the addition of acids and inorganic salts were investigated. The products were characterized by field emission scanning electron microscopy (FESEM) coupled with energy-dispersive X-ray spectroscopy (EDX), and transmission electron microscopy (TEM). The results show that the nanoparticles of ZnS were obtained in hydrochloric acid and acetic acid addition. The diameters were in the range of 10 to 20 nm and 50 to 100 nm, respectively. In the case of a sodium chloride salt addition, a ZnS structure was obtained with a particle size of approximately 5 nm and a flake-like morphology.


2013 ◽  
Vol 750-752 ◽  
pp. 336-339
Author(s):  
Fa Chao Wu ◽  
Teng Fei Shen

In this work, CaCO3 nanoparticles have been synthesized via heat-treatment of a new precursor. Effect of calcinations temperature on particle size has been investigated. The products were characterized by Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). nanoCaCO3 was modified using chloroform as solvent and fatty acid as modifier atroom temperature. The advantage of this modification is that it can be proceed at room temperature and it can reduce energy consumption.


NANO ◽  
2016 ◽  
Vol 11 (07) ◽  
pp. 1650079 ◽  
Author(s):  
Wenjun Yan ◽  
Ming Hu ◽  
Jiran Liang ◽  
Dengfeng Wang ◽  
Yulong Wei ◽  
...  

A novel composite of Au-functionalized porous silicon (PS)/V2O5 nanorods (PS/V2O5:Au) was prepared to detect NO2 gas. PS/V2O5 nanorods were synthesized by a heating process of pure vanadium film on PS, and then the obtained PS/V2O5 nanorods were functionalized with dispersed Au nanoparticles. Various analytical techniques, such as field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), have been employed to investigate the properties of PS/V2O5:Au. Herein, the PS/V2O5:Au sample exhibited improved NO2-sensing performances in response, stability and selectivity at room temperature (25[Formula: see text]C), compared with the pure PS/V2O5 nanorods. These phenomena were closely related to not only the dispersed Au nanoparticles acting as a catalyst but also the p-n heterojunctions between PS and V2O5 nanorods. Whereas, more Au nanoparticles suppressed the improvement of response to NO2 gas.


2012 ◽  
Vol 602-604 ◽  
pp. 183-186 ◽  
Author(s):  
Jing Liu ◽  
Rong Wu ◽  
Jin Li ◽  
Yan Fei Sun ◽  
Ji Kang Jian

In this paper, we report the synthesis of cubic silicon carbide (3C-SiC) nanoparticles by direction reaction of silicon powders and carbon nanotubes. The as-prepared SiC nanoparticles were characterized by X-ray powder diffraction, scanning electron microscopy, transmission electron microscopy and Raman scattering at room temperature. The possible growth mechanism is proposed.


2008 ◽  
Vol 575-578 ◽  
pp. 941-946
Author(s):  
Hong Yan Tang ◽  
Ji Hui Wang ◽  
Guo Qiang Gao ◽  
Wen Xing Chen

Fiberglass continuous strand mat(CSM)/poly(urethane-isocyanurate) composites were formed by SRIM process, treated under different conditions and then characterized based on dynamic mechanical thermal analysis (DMTA), differential scanning calorimetry (DSC), scanning electron microscopy (SEM) ,transmission electron microscopy (TEM) and the mechanical property tests. The results show that the mechanical properties of the composites could be increased with improving the degree of microphase separation. At a given temperature (120°C), the degree of microphase separation is the highest for 4h and decreases gradually with prolonging treatment time. For a given time (4h), the well microphase-separated morphology is obtained and the degree of microphase mixing is increased at 120°C and 140°C treatments, respectively. The degree of microphase separation of the composites decreases with enhancing the temperature to 140°C.


2014 ◽  
Vol 1035 ◽  
pp. 488-491
Author(s):  
Jing Jing Li ◽  
Yun Zhao ◽  
Han Sheng Li ◽  
Qin Wu ◽  
Qing Ze Jiao

Hollow nickel ferrite microspheres with a diameter of about 1.5 to 2.5 μm were synthesized using an emulsion-based solvothermal method in combination with calcination at 550°C. The structures and morphologies of the nickel ferrite microspheres were characterized using an X-ray diffractometer, a transmission electron microscopy and a field emission scanning electron microscopy. Magnetization measurement was carried out using a vibrating sample magnetometer at room temperature. The saturation magnetization and coercivity of nickel ferrite microspheres could reach 19.41 emu/g and 202.28 Oe, respectively. Hollow nickel ferrite microspheres might be used as catalysts, magnetic materials and microwave absorbers.


Author(s):  
Robert W. Weise

The role that scanning electron microscopy (SEM) is playing in descriptive helminthology is becoming more apparent in the literature. However, the majority of papers on the SEM of helminths have used conventional or modified light microscope techniques of fixation and dehydration, and not established SEM techniques in which freeze- and critical point-drying are routinely used. The present investigation was undertaken to examine the applicability of modified scanning and transmission electron microscope techniques for the preparation of certain helminths for SEM.Method I.– Live animal-parasitic nematodes were fixed in 6% phosphate buffered glutaraldehyde for 24 hr at room temperature.


Author(s):  
P Walther ◽  
P Herter ◽  
J Hentschel ◽  
H Hentschel

The kidney is a complex zonated organ with a variety of different cell types. For the study of the functional and morphological features, the precise localization in the zones is relevant, which requires the evaluation of rather large portions of tissue. Transmission electron microscopy of replicas of tissue is limited by difficulties to obtain sufficiently large specimens. In order to overcome this problem cryopreparation methods and high resolution field emission scanning electron microscopy (SEM) were used.1 mm3 cubes of perfusion fixed rabbit kidneys cryoprotected with glycerol were frozen by plunging into liquid propane. For further preparation two different methods were employed.1: Samples were fractured in liquid nitrogen with a scalpel, freeze substituted using methanol with glutaraldehyde and osmiumtetroxid, warmed to room temperature, critical point dried, and coated by electron gun evaporation with 2 nm of platinum at an angle of 45°, and 10 nm of carbon perpendicularly.


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