Prediction of grain size for large-sized aluminium alloy 7050 forging during hot formingYi, You-ping; Fu, Xin; Cui, Jin-dong; Chen, Hua
doi: 10.1007/s11771-008-0001-3pmid: N/A
A numerical approach for process optimization and microstructure evolution of lager-sized forging of aluminium alloy 7050 was proposed, which combined a commercial FEM code Deform 3D with empirical models. To obtain the parameters of empirical constitutive equation and dynamic recrystallization models for aluminium alloy 7050, the isothermal compression tests of 7050 samples were performed on Gleeble-1500 thermo-simulation machine in the temperature range of 250–450 °C and strain rate of 0.01–10 s−1, and the metallograph analysis of the samples were carried out on a Leica DMIRM image analyzer. The simulation results show that the dynamic recrystallization in the central area of the billet occurs more easily than that on the edge. Repetitious upsetting and stretching processes make the billet deform adequately. Among several forging processes e.g. upsetting, stretching, rounding and flatting, the stretching process is the most effective way to increase the effective strain and refine the microstructure of the billet. As the forging steps increase, the effective strain rises significantly and the average grain size reduces sharply. Recrystallized volume fractions in most parts of the final forging piece reach 100% and the average grain size reduces to 10 μm from initial value of 90 μm.
Directional migration behavior of cerium during sintering process of mischmetal doped cemented carbideZhang, Li; Chen, Shu; Xiong, Xiang-jun; Yu, Xian-wang; Wang, Yuan-jie
doi: 10.1007/s11771-008-0002-2pmid: N/A
Three observation methods were used to investigate the existing form and the behavior of rare earth during the sintering process of high activity mischmetal (RE, with lanthanum and cerium) doped WC-8%Co-0.048%RE(mass fraction) alloy with low carbon-containing level by scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDXS), considering the fact that the addition amount of rare earth in the alloy is very minute. The directional migration process and mechanism of cerium were discussed. First, the sinter skin (surface) is observed. It is shown that there exists a dispersedly distributed cerium containing oxide on the sinter skin, and lanthanum in these cerium enrichment positions is very minute. Secondly, the polished section is observed, and lanthanum containing phase/micro-zone in the alloy is identified. Finally, based on the fact that the fracture of cemented carbide is resulted from the heterogeneous phase or other defects within the microstructure, the fracture surface is observed and cerium containing phase/micro-zone in the fracture source approximately 260 μm from the surface is identified. These combined observations reveal adequately the fact that lanthanum and cerium get separated and cerium predominantly migrates towards the surface during the sintering process.
Microstructures and magnetic properties of [SiO2/FePt]5/Ag thin filmsFan, Jiu-ping; Xu, Xiao-hong; Jiang, Feng-xian; Tian, Bao-qiang; Wu, Hai-shun
doi: 10.1007/s11771-008-0003-1pmid: N/A
[SiO2/FePt]5/Ag thin films were deposited by RF magnetron sputtering on the glass substrates and post annealing at 550 °C for 30 min in vacuum. Vibrating sample magnetometer and X-ray diffraction analyser were applied to study the magnetic properties and microstructures of the films. The results show that without Ag underlayer [SiO2/FePt]5 films deposited onto the glass are FCC disordered; with the addition of Ag underlayer [SiO2/FePt]5/Ag films are changed into L10 and (111) mixed texture. The variation of the SiO2 nonmagnetic layer thickness in [SiO2/FePt]5/Ag films indicates that SiO2-doping plays an important role in improving the order parameter and the perpendicular magnetic anisotropy, and reducing the grain size and intergrain interactions. By controlling SiO2 thickness the highly perpendicular magnetic anisotropy can be obtained in the [SiO2 (0.6 nm)/FePt (3 nm)]5/Ag (50 nm) films and highly (001)-oriented films can be obtained in the [SiO2 (2 nm)/FePt (3 nm)]5/Ag (50 nm) films.
Synthesis of carbon nanofibers by ethanol catalytic combustion techniqueLi, Fei; Zou, Xiao-ping; Cheng, Jin; Zhang, Hong-dan; Ren, Peng-fei; Wang, Mao-fa; Zhu, Guang
doi: 10.1007/s11771-008-0004-0pmid: N/A
A general, simple and economic synthetic method for synthesizing carbon nanofibers was presented. In the method, ethanol was employed as carbon source; metal salts such as nickel nitrate, ferric nitrate and ferric chloride were used as catalyst precursor respectively; copper plate was employed as the support material. A lot of products were obtained by catalytic combustion deposition of ethanol vapor. Then the as-prepared carbon nanofibers were characterized by field-emission scanning electron microscopy, transmission electron microscopy, Raman spectroscopy, energy dispersion X-ray spectroscopy and selected-area electron diffractometry. By analyzing the results of characterization, the conclusions are as follows: 1) the large catalyst particles tend to form large-diameter CNFs, small catalyst particles are inclinable to form small-diameter CNFs; 2) the morphology of the catalyst can affect the final morphology of the CNFs. Moreover, the possible growth mechanisms were proposed and the degree of graphitization of samples was estimated by Raman spectroscopy characterization.
Resistance optimization of flexes in aluminum reduction cellsLi, Jie; Liu, Jie; Liu, Wei; Lai, Yan-qing; Wang, Zhi-gang; Wu, Yu-yun
doi: 10.1007/s11771-008-0005-zpmid: N/A
The resistance arrangements of the flexes connecting with the cathode bus bar in aluminum reduction cells were generalized as three modes. In each mode the universal method to select proper resistivity of the flexes was induced respectively to insure that the current in local group of flexes was equal. Furthermore, a 350 kA aluminum reduction cell based electric field model was developed by finite element method to evaluate the effect of the method. Suggestions on selection of three modes were also put forward. The results show that the methods of resistance optimization can reduce the current variation about 180 A compared with that in original case.
Effect of CaO doping on mechanical properties and thermal shock resistance of 10NiO-NiFe2O4 composite ceramicsLai, Yan-qing; Zhang, Yong; Zhang, Gang; Tian, Zhong-liang; Li, Jie
doi: 10.1007/s11771-008-0006-ypmid: N/A
The CaO doped 10NiO-NiFe2O4 composite ceramics were prepared by the cold isostatic pressing-sintering process, and the effects of CaO content on the phase composition, mechanical property and thermal shock resistance of 10NiO-NiFe2O4 composite ceramics were studied. The results show that the samples mainly consist of NiO and NiFe2O4 when content of CaO is less than 4%(mass fraction), bending strength increases obviously by CaO doping. Bending strength of the samples doped with 2% CaO is above 185 MPa, but that of the samples without CaO is only 60 MPa. Fracture toughness is improved obviously by CaO doping, the samples doped with 2% CaO have the maximum fracture toughness of 2.12 MPa ·m1/2, which is about two times of that of the undoped ceramics. CaO doping is bad to thermal shock resistance of 10NiO-NiFe2O4 composite ceramics.
Preparation of spherical and dense LiNi0.8Co0.2O2 lithium-ion battery particles by spray pyrolysisHu, Guo-rong; Deng, Xin-rong; Peng, Zhong-dong; Cao, Yan-bin; Liu, Zhi-min; Liu, Ye-xiang
doi: 10.1007/s11771-008-0007-xpmid: N/A
With citric acid as a polymeric agent layered LiNi0.8Co0.2O2 materials were synthesized by a spray pyrolysis method. The LiNi0.8Co0.2O2 particles were characterized by means of XRD, SEM and TEM. The electrochemical performances of LiNi0.8Co0.2O2 particles were studied in a voltage window of 3.00–4.35 V and at a current density of 30 mA/g. The results show that in the pilot-scale spray pyrolysis process, the morphology of particles is dependent upon the precursor concentration and flux of carrier gas. The initial discharge capacity of the LiNi0.8Co0.2O2 particles at 720 °C for 12 h °C is 187.3 mA·h/g, and the capacity remains 96.8 % with excellent cycleability after 30 cycles. The LiNi0.8Co0.2O2 samples synthesized under the optimized conditions by the spray pyrolysis method shows a good electrochemical performance.
Coating of LiNi1/3Mn1/3Co1/3O2 cathode materials with alumina by solid state reaction at room temperaturePeng, Zhong-dong; Deng, Xin-rong; Du, Ke; Hu, Guo-rong; Gao, Xu-guang; Liu, Ye-xiang
doi: 10.1007/s11771-008-0008-9pmid: N/A
Alumina coated LiNi1/3Mn1/3Co1/3O2 particles were obtained by a simple method of solid state reaction at room temperature. The reaction mechanism of solid state reaction at room temperature was investigated. The structure and morphology of the coating materials were investigated by XRD, SEM and TEM. The electrochemical performances of uncoated and Al2O3-coated LiNi1/3Co1/3Mn1/3O2 cathode materials were studied within a voltage window of 3.00–4.35 V at current density of 30 mA/g. SEM, TEM and EDS analytical results indicate that the surface of LiNi1/3Mn1/3Co1/3O2 particles is coated with very fine Al2O3 composite, which leads to the improved cycle ability though a slight decrease in the first discharge capacity is observed. It is proposed that surface treatment by solid state reaction at room temperature is a simple and effective method to improve the cycle performance of LiNi1/3Co1/3Mn1/3O2 particles.
Fabrication of ferrocenyl glutathione modified electrode and its application for detection of cadmium ionsWang, Fang-bin; Fan, Mei-yi; Liu, You-nian; Wang, Jian-xiu; Zeng, Dong-ming; Huang, Ke-long
doi: 10.1007/s11771-008-0010-2pmid: N/A
1′-cysteaminecarbonyl-1-glutathionecarbonyl-ferrocene (Fc-GSH) was synthesized from ferrocene dicarboxylic acid and reduced glutathione (GSH) with 4 steps. IR and 1H-NMR were used to characterize the products. Then Fc-GSH was immobilized on the surface of gold electrode. Cyclic votammetry (CV) was adopted to investigate the electrochemical properties of this Fc-GSH modified electrode in the absence and presence of Cd2+ aqueous solutions. The peak oxidation potential (E
a) and reduction potential (E
c) of Fc-GSH modified electrode were observed at E
a = 0.74 V and E
c = 0.64 V (vs Ag/AgCl) before the accumulation of Cd2+. This redox process is a monoelectron chemical reaction. The anodic shift is about 80 mV in the presence of 20 nmol/L of Cd2+ aqueous solution. Moreover, this shift is in proportion to the concentration of Cd2+ when the concentration of Cd2+ is lower than 20 nmol/L. So the modified electrode can be used as probes to detect cadmium ions with the limit of 0.1 nmol/L by cyclic voltammetry.