Deformation of the Aluminum Bath Surface in an Induction Melting Furnace

2015 ◽  
pp. 997-1004
Author(s):  
Akshay Bansal ◽  
Pierre Chapelle ◽  
Yves Delannoy ◽  
Emmanuel Waz ◽  
Pierre Le Brun ◽  
...  
2015 ◽  
pp. 999-1004
Author(s):  
Akshay Bansal ◽  
Pierre Chapelle ◽  
Yves Delannoy ◽  
Emmanuel Waz ◽  
Pierre Le Brun ◽  
...  

2007 ◽  
Vol 334-335 ◽  
pp. 297-300
Author(s):  
Si Young Sung ◽  
Bong Jae Choi ◽  
Young Jig Kim

The aim of this study is to evaluated the possibility of the in-situ synthesized (TiC+TiB) reinforced titanium matrix composites (TMCs) for the application of structural materials. In-situ synthesis and casting of TMCs were carried out in a vacuum induction melting furnace with Ti and B4C. The synthesized TMCs were characterized using scanning electron microscopy, an electron probe micro-analyzer and transmission electron microscopy, and evaluated through thermodynamic calculations. The spherical TiC plus needle-like and large, many-angled facet TiB reinforced TMCs can be synthesized with Ti and B4C by a melting route.


2018 ◽  
Vol 108 (11-12) ◽  
pp. 760-766
Author(s):  
S. Mohammadifard ◽  
J. Langner ◽  
M. Stonis ◽  
S. Sauke ◽  
H. Larki Harchegani ◽  
...  

In einem Aluminium (Al)-Schmelzofen sind der Füllstand des Schmelzbades und die Oxidschichtmenge mit Kontaktsensoren nicht überwachbar, da das Schmelzbad aufgrund der hohen Haltebereich-Temperaturen von über 600 °C nicht zugänglich ist. Deshalb wird ein Online-Überwachungssystem des Aluminium-Schmelzbades mithilfe optischer Sensoren erforscht. Dafür wird das Schmelzbad mit geeigneten optischen Messsystemen identifiziert. Schließlich werden durch Bildanalyse-Algorithmen die Höhenänderung der Schmelze herausgearbeitet. Zudem werden Oxidschichten im Ofen auf der Badoberfläche mithilfe der Algorithmen detektiert.   The melt level and oxide layer quantity in an aluminum melting furnace cannot be monitored by contact sensors, since the melting bath is not accessible due to the high holding temperature (above 600 °C). Therefore, the method of monitoring the melting bath by means of optical sensors is investigated for the first time. For this purpose, suitable optical measuring systems can be applied which will be able to record the melting bath. The height change of the melt is to be elaborated by means of image analysis and any oxide layer on the bath surface is to be detected.


2014 ◽  
Vol 13 (05n06) ◽  
pp. 1460003
Author(s):  
Zhaojiang Liu ◽  
Lei Huang ◽  
Qi Wan ◽  
Xu Li ◽  
Ma Guang ◽  
...  

La 0.75 Mg 0.25 Ni 3.5 Si 0.10 hydrogen storage alloy was prepared by vacuum induction melting furnace and subsequently heated treatment at 940°C for 8 h and cooled to room temperature in the oven. The electrochemical properties of La 0.75 Mg 0.25 Ni 3.5 Si 0.10 compound were measured by LAND CT2001A battery test system. The morphologies of the samples were characterized by scanning electron microscopy (SEM). The surface state of samples was analyzed by X-ray photoelectron spectroscopy (XPS). It was found that the charge–discharge rate plays the key impact on the cycling stability of the alloy. During the cycle test, the prepared La 0.75 Mg 0.25 Ni 3.5 Si 0.10 compound presented an excellent capacity retention at the charge–discharge of 1 C while the capacity of sample declined rapidly at 0.2 C. The excellent cycling stability performance of La 0.75 Mg 0.25 Ni 3.5 Si 0.10 electrode at 1 C could be attributed to the less powder and less oxidation of surface effective active elements. The pulverization inevitably leads to the separation of the part of the cracking alloy and the electrode, resulting in reduction of the effective active substance and increasing attenuation of the capacity per cycle. In addition, on the analysis of the different cut-off potential effects on the electrode, it was found that the La 0.75 Mg 0.25 Ni 3.5 Si 0.10 electrode shows good comprehensive electrochemical properties at 1 C cut-off 0.6–0.7 V. During charging, heavy overcharge will not be conducive to cycling stability performance during the charging test.


2011 ◽  
Vol 675-677 ◽  
pp. 101-104
Author(s):  
Qi Zhi Xing ◽  
Wei Dong ◽  
Shu Ang Shi ◽  
Guo Bin Li ◽  
Yi Tan

Multi-crystalline silicon ingots were prepared by directional solidification using vacuum induction melting furnace. The content of aluminum and iron deeply decreased in the columnar crystal region of the multi-crystalline silicon ingots. The columnar crystal growth broke off corresponded to the iron contents sharply increased. The height of columnar crystal in the silicon ingots related to the pulling rates had been clarified by the constitutional supercooling theory. The maximum of the resistivity and the minority carrier lifetime closed to the transition zone where the conductive type changed from p-type to n-type in silicon ingots. Further analysis suggested that the electrical properties were related to the contents of shallow level impurities aluminum, boron and phosphorus.


2012 ◽  
Vol 717-720 ◽  
pp. 37-40 ◽  
Author(s):  
Ta Ching Hsiao ◽  
Sheng Tsao

Silicon carbide powders were prepared in a vacuum induction melting furnace (VIM). Silica and silicon were used as sources of silicon, and graphite powder was used a source of carbon. Pressures of 0.1 and 0.01 atm were selected as the operation conditions, and different silicon carbide powders were prepared. Free carbon and remnant silica were removed by high-temperature baking in air and acid leaching. Low-pressure powders show better crystallinity; moreover, free carbon and silica were rarely found in the product after baking and leaching. The low-pressure grains were prismatic whereas the high-pressure grains were porous. This shows that pressure is a critical parameter in silicon carbide formation, and low-pressure makes the low-temperature synthesis of silicon carbide feasible. Glow discharge mass spectra were used to analyze the impurity content in silicon carbide powders. After baking and leaching, the purity is increased from 3N5 (99.95 wt.%) to 4N5 (99.995 wt.%). Further purification procedures will be combined to meet the quality requirements for crystal growth.


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