Film-forming material
a film-forming material and film-forming technology, applied in the field of film-forming materials, can solve the problems of increasing the demand for improving the corrosion resistance of film-forming materials against halogen-based plasma, and achieve the effect of high deposition rate and high corrosion resistan
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example 1
Step 1: Mixing of Raw Materials
[0090]First, 100 mol of yttrium oxide Y2O3 powder (D50d=3.2 μm) manufactured by Nippon Yttrium Co., Ltd. and 200 mol of yttrium fluoride YF3 powder (D50d=5.6 μm) manufactured by Nippon Yttrium Co., Ltd. were mixed, and ethanol serving as a solvent for mixing was added to the mixed powder to give a slurry having a solid concentration of 50%. This slurry was subjected to wet grinding using a DYNO-MILL ECM-AP2 (wet bead mill) from Willy A. Bachofen such that D50α of particles after mixing treatment, as determined on a Microtrac (registered trademark) HRA using a method below, was 3 μm or less (specifically, 2.5 μm). The slurry after the wet grinding was dried at 120° C. for 12 hours to give a dry product.
Method for Determining D50α
[0091]About 1 g of ground powder was put in a 100-mL glass beaker, and a 0.2% aqueous solution of sodium hexametaphosphate serving as a dispersion medium was then put in the beaker to the line of 100 mL to prepare a slurry for d...
example 2
[0111]A film-forming material in granular form was obtained in the same manner as in Example 1 except that, in Step 1, the DYNO-MILL ECM-AP2 was replaced by a wet ball mill, and wet grinding was performed such that D50α after mixing treatment as determined on the Microtrac HRA using the above-described method was 2.4 μm. With respect to the obtained film-forming material. D50, the relative intensities of the X-ray diffraction peaks, and the oxygen content were determined in the same manner as in Example 1. Table 2 shows the results. Also, a film was formed from the obtained film-forming material in the same manner as in Example 1.
example 3
[0112]A film-forming material in granular form was obtained in the same manner as in Example 1 except that, in Step 1, instead of ethanol, 1-propanol was used as the solvent for mixing. With respect to the obtained film-forming material, D50, the relative intensities of the X-ray diffraction peaks, and the oxygen content were determined in the same manner as in Example 1. Table 2 shows the results. Also, a film was formed from the obtained film-forming material in the same manner as in Example 1.
PUM
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