8" inch ceramic chuck table
12" inch ceramic chuck table
REPAIR OR REBUILD ACCRETECH/TSK DICING MACHINE CHUCK TABLE MACHINE MODLE ACCRETECH / TSK 2500 |
ACCRETECH / TSK 88 A |
ACCRETECH / TSK APM-5000 |
ACCRETECH / TSK APM-6000A |
ACCRETECH / TSK APM-60B |
ACCRETECH / TSK APM-90AL |
ACCRETECH / TSK AWD-100A |
ACCRETECH / TSK AWD-100A(M) |
ACCRETECH / TSK AWD-10A |
ACCRETECH / TSK AWD-110M |
ACCRETECH / TSK AWD-200T |
ACCRETECH / TSK AWD-208T |
ACCRETECH / TSK AWD-300T |
ACCRETECH / TSK AWD-4000A |
ACCRETECH / TSK AWD-4000B |
ACCRETECH / TSK AWD-5000 |
ACCRETECH / TSK AWD-5000A |
ACCRETECH / TSK G-SL-534A-CX |
ACCRETECH / TSK MSP 90A |
ACCRETECH / TSK PSM-2000A |
ACCRETECH / TSK UF 170 |
ACCRETECH / TSK UF 200 / 200A |
ACCRETECH / TSK UF 200FL |
ACCRETECH / TSK UF 200SFL |
ACCRETECH / TSK UF 300/300A www.chuck-table.com |
前工序工艺设备: | |
Ultratech Stepper Model 1700 C-V 图示仪(电容/电压曲线测量仪) 少数载流子寿命测试仪 尘埃颗粒测量仪KLA Tencor5500,6200,SP1 膜厚测试仪 Nanospec 180/181/210 台阶仪:Tencor AlphaStep 200/300/500 | |
后工序设备 | |
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硅片生产设备: | |
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ZERODUR
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ZERODUR® is a glass ceramic characterized by a phase of evenly distributed nano-crystals within a residual glass phase. It contains around 75 weight percent crystalline phase with a high quartz structure. The crystal structure has a negative linear thermal expansion, while the other glass phase has a positive linear thermal expansion. The material is adjusted in a way that the positive thermal expansion of the glass phase and the negative thermal expansion of crystal structure effectively neutralize each other. The crystals are typically only 50 nm in diameter, and ZERODUR appears reasonably transparent because the refractive indices of the two phases are almost identical. The most important properties of zerodur are:
Figure 1&2 and table 1 give an overview of ZERODUR’s properties.
Low Expansion Materials :
ZERODUR® is a registered trademark of Schott Glass Technologies.
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Material Properties for Alumina Ceramics | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Generally, porous ceramics are fabricated in accordance with two procedures as follows:First, a ceramic is mixed with a pyrolyzable material or volatile material. Thereafter, gases are evolved by the pyrolysis of the pyrolyzable material or volatilizing the volatile material, and the evolving gases form pores in the ceramic to fabricate a porous ceramic (see, e.g., U.S. Pat. Nos. 5,358,910and 5,750,449).In summary, after a ceramic and a preceramic polymer are mixed with each other by a ball milling process, the mixture is molded into a desired shape. The molded body is heated to fire combustible components and volatilize volatile components contained in the preceramic polymer (pyrolysis). The ceramic components contained in the molded body are sintered by heating, and the volatile components contained in the preceramic polymer are volatilized to form pores within the molded body, thereby fabricating a final porous ceramic.However, this method has a disadvantage that when the content of the polymeric components is not less than 50%, the shape of the molded body may collapse due to softening and pyrolysis of the polymeric components. Accordingly, it is difficult to fabricate highly porous ceramics having a porosity of 70% or more. Further, uniform distribution of pores is difficult to obtain and pore size cannot be easily controlled according to the material properties.Second, a porous ceramic can be fabricated by lowering the sinterability of a ceramic. This method is divided into the following two procedures. The first method is carried out by sintering a ceramic below optimum sintering temperature to lower the relative density of the ceramic, thereby forming more pores within the ceramic. However, since the porous ceramic thus fabricated is not sintered at optimum sintering conditions, mechanical properties such as strength may be greatly deteriorated.
AbstractAn improved gel-casting procedure was successfully exploited to produce porous ceramic bodies having controlled porosity features in terms of mean pore size, total pore volume as well as pore geometry. The gel-casting process in which a natural gelatine for food industry is used as gelling agent was firstly set-up to prepare dense alumina and zirconia components. Then, commercial PE spheres, sieved to select proper dimensional ranges, were added to the starting slurries as pore-forming agent. Both alumina and zirconia porous bodies were then produced, having a porosity ranging between 40 and 50 vol%. The fired components were characterised by spherical pores surrounded by highly dense ceramic walls and struts, having a homogeneous and fine microstructure. Their mean pore size was directly dependent on the sieved fraction of the starting PE spheres selected as pore-forming phase.