The role of texture in the electromigration behavior of pure aluminum lines

1996 ◽  
Vol 79 (5) ◽  
pp. 2409-2417 ◽  
Author(s):  
D. B. Knorr ◽  
K. P. Rodbell
Keyword(s):  
2013 ◽  
Vol 668 ◽  
pp. 865-869
Author(s):  
Wan Wu Ding ◽  
Wen Jun Zhao ◽  
Tian Dong Xia

The influence of different solidified velocities on the structure of pure aluminum during the process of refinement by Al-5Ti-0.6C master alloy was studied and the impact mechanism was discussed. The results show that at the same solidified velocity, with the increase of the amount of Al-5Ti-0.6C master alloy, in the solidified structure of pure aluminum, columnar crystals will gradually decrease, while equiaxed crystals will gradually increase. But in the case when the level of addition is the same, the faster the solidified velocity, the greater the number of equiaxed crystals will be in the ingot microstructure. The formation of equiaxed crystals is the result of the dual role of dissociation of crystal particles and heterogeneous nucleation of “TiC particle---Ti transition zone”.


2011 ◽  
Vol 311-313 ◽  
pp. 1814-1817
Author(s):  
Guo Ning Liu ◽  
Hua Dong Zhao ◽  
He Zheng Wang ◽  
Jing Ru Dong ◽  
Ming Hao Zhao

Polyester textiles usually have excellent mechanical properties. However, their mechanical behaviors under extreme conditions such as in the environment with high ozone concentration usually decay after a certain time period. Aiming at increasing the mechanical behavior of commercial polyester textiles under extreme conditions, a PET thin film coated with pure aluminum (Al) on its surface has been introduced as the top layer of the fabricated material with polyester textile as the middle layer. Main purpose of the study is to evaluate the role of aluminum thin film on the surface in improving the mechanical behavior of the polyester textiles after they have been exposed in the environment with extremely high concentration of ozone gas.


2018 ◽  
Vol 36 (1) ◽  
pp. 35-54 ◽  
Author(s):  
Hideaki Takahashi ◽  
Makoto Chiba

AbstractAnodic oxide films on aluminum are classified into two groups: porous-type anodic oxide films (PAOF) and barrier-type anodic oxide films (BAOF). The present paper is a review of the corrosion of pure aluminum (Al) and Al alloys covered with PAOF and BAOF, focusing on the role of anodic oxide films in the process of corrosion. Several topics are discussed in detail, including (a) changes in the dissolution mode of PAOF in acidic media by pore sealing, (b) hydration and dissolution of BAOF in pure water and neutral solutions containing organic and inorganic electrolytes, (c) pitting corrosion during the cathodic polarization of Al covered with PAOF and BAOF, (d) corrosion of PAOF-covered Al/Bi/Sn alloys in alcohols at 142°C, and (e) synergistic effects of Cl− and Cu2+ ions in the corrosion of PAOF-covered Al alloys in aqueous solutions.


1986 ◽  
Vol 108 (4) ◽  
pp. 502-513 ◽  
Author(s):  
K. Komvopoulos ◽  
N. Saka ◽  
N. P. Suh

Analytical and experimental studies were conducted on oxidized and nonoxidized pure aluminum, OFHC copper, and electroplated chromium to investigate the role of surface oxide layers in boundary lubrication. The effects of the thickness of the oxide layers, the elastic moduli of the oxide and the metal, and the normal surface traction have been addressed. In addition, several possible failure mechanisms of both thin and thick oxide films have been proposed. The experimental results have shown that low coefficients of friction, about 0.1 or less, and especially low wear can be obtained in boundary-lubricated sliding if the metal surfaces are protected from plastic deformation by sufficiently thick oxide layers. Scanning electron microscopy has shown that when the oxide layers are not ruptured, the wear of the surfaces is negligibly small. In this case, the oxide-oxide contacts deform primarily elastically and the predominant friction mechanism is the shear of the lubricant film. Based on this evidence, a theoretical model for friction was proposed and the agreement between theoretical and experimental coefficients of friction was reasonably good. Disruption of the oxide layers during sliding, however, was found to result in plastic deformation and plowing of the surfaces.


2018 ◽  
Vol 2018 ◽  
pp. 1-8 ◽  
Author(s):  
Viet Q. Vu ◽  
Yan Beygelzimer ◽  
Roman Kulagin ◽  
Laszlo S. Toth

A new severe plastic deformation (SPD) process called plastic flow machining (PFM) was recently proposed to produce thin sheets with gradient structures. In the present paper, the role of the die geometry is investigated by studying the effects of the produced sheet thickness (h) on the material properties of commercial pure Aluminum (Al1050) processed by PFM. The obtained experimental results show that an increase of h in the range of 0.65 to 1.5 mm improved the formation efficiency of the sheet. Microstructures of the produced sheets show gradient structures with an average grain size varying from 0.8 to 3.81 µm across the sheet thickness. Both experiments and finite element (FE) simulations document that the degree of the gradient in the microstructure became more significant when h was increased. Sheets produced by PFM exhibited a better strength-ductility balance than sheets obtained in other SPD processes. Tensile strength of 160–175 MPa and total ductility of 18–25% were obtained for the processed samples after PFM. A rise of h from 0.65 to 1.5 mm lowered the strength but enhanced the ductility of the produced sheet, which is due to the coarser microstructure at larger values of h.


2010 ◽  
Vol 649 ◽  
pp. 385-390 ◽  
Author(s):  
Kota Kadoi ◽  
Norbert Babcsán ◽  
Hideo Nakae

The aim of this work is to elucidate the role and contribution of oxide particles to aluminum foam fabrication. The melts were internally oxidized by a thickening process in which pure aluminum melt was stirred with or without the addition of 1.5 wt.% calcium for maximum 25 min. After this, each thickened samples were melted again and mixed for 100 s by introducing 1.5 wt.% TiH2 as a blowing agent. In order to investigate the foam evolution, the foam samples were hold in the furnace for 50 to 500 s. The stirring torque (viscosity) of the calcium containing melt increases with thickening time and achieves the stationary value after 17 min. However, the torque of pure aluminum melt does not change during stirring. Oxides have been found on the microstructures of both stirred samples, although the content of oxides of calcium added sample is significantly more than that of pure aluminum. SEM observation results of samples thickened by calcium addition show that the melt contains calcium oxide and Al4Ca in addition to equiaxed aluminum, and the morphology of formed oxide is not granulous but wrinkled bifilm containing calcium and aluminum oxides. The oxides formed in the pure Al melt has less effect on the viscosity thus the foamability of the aluminum melt. It is found that the calcium oxides formed by stirring are responsible for the effective increase of melt viscosity. The foams using oxidized pure Al melt have dense layer at the bottom caused by drainage and coarse foam structure due to strong coalescence. In case of the Al-Ca alloy, uniform pore distribution, lack of the dense layer and homogeneous time dependent increase of the cell size were observed. Besides, the sample held for longer time has thicker cell wall at the bottom compared with that at the top. We confirmed that the oxide bifilms of Al and Ca contributes to decreased drainage rate and coalescence, namely stabilization. The insufficient amount of oxide particles in pure aluminum is the reason for the lack of stabile foam (significant drainage) in that case.


2012 ◽  
Vol 476-478 ◽  
pp. 388-391
Author(s):  
Guo Ning Liu ◽  
Hua Dong Zhao ◽  
He Zheng Wang ◽  
Xian Zhong Xu ◽  
Ming Hao Zhao

Though composites, particularly those consisting of organic materials, have replaced the role of traditional metallic materials in various engineering applications due to their relatively high mechanical strength, low density, flexibility and low cost, their disadvantages caused by relatively high porosity ratio and low crystallinity inherently make this kind of materials the less favorable choices when low permeation property is a major criterion. Here pure aluminum (Al) thin film, which has excellent anti-corrosion property, is introduced into the structure of fabricated composites to improve the composite’s anti-permeation behavior in corrosive environment while the advantageous points of organic composites are exploited at the same time by applying the optimized thermo-mechanical processing techniques in fabrication. Thus greater potentials for organic polymeric composites may be achieved in the future.


2013 ◽  
Vol 652-654 ◽  
pp. 1072-1075 ◽  
Author(s):  
Wan Wu Ding ◽  
Jiang Tao Zhu ◽  
Wen Jun Zhao ◽  
Tian Dong Xia

The grain refining effects of Al-Ti, Al-TiC and Al-Ti-C master alloys on commercially pure aluminum were compared, and the grain refinement mechanism of TiAl3 and TiC among master alloys was discussed. The results show that: the grain refinement of the master alloys Al-TiC and Al-Ti toward pure aluminum mainly stems from the heterogeneous nucleation role of TiC and TiAl3 particles, but with the extension of heat preservation time of fused mass, its role of heterogeneous nucleation will decline due to dissolution of TiAl3 and aggregation and precipitation of TiC. The preferable grain refinement effects of Al-Ti-C master alloys toward pure aluminum are mainly due to the fact that when TiAl3 and TiC particles are acted commonly as heterogeneous nucleation particles, the heterogeneous nucleation effect of TiC particles will be enhanced because of the presence of TiAl3.


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