Method for rapidly sintering fully stabilized zirconia powder under low temperature and normal pressure
A fully stabilized zirconia and rapid sintering technology, applied in the field of fine chemicals, can solve the problems of increased production cost and long sintering cycle of FSZ materials, and achieve the effect of ensuring performance, solving densification and grain coarsening, and improving performance.
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Embodiment 1
[0035] Such as figure 1 As shown, first set Y 2 o 3 Dissolve with concentrated nitric acid to form 0.2mol?l -1 Stable and transparent Y(NO 3 ) 3 solution. At the same time, zirconium sulfate was dissolved in distilled water to form 0.2mol?l -1 Stable clear solution. Then the above two solutions according to (Y 3+ :Zr 4+ ) with a molar ratio of 3:97, and adjust the pH value to 7 with ammonia water. Add a slightly excess saturated urea solution and heat to 75°C, causing the solution to completely precipitate and form a uniform and stable co-precipitation product; then, wash the co-precipitation product, dry it at 90°C and dry it at 600°C The heat treatment was carried out for 2 h, and the precursor was obtained after natural cooling. Then the precursor was mixed with 0.6mol?l -1 CaCl 2 -MgCl 2 Composite molten salt (CaCl 2 / MgCl 2 Molar ratio is 0.474:0.526) solution by (Ca 2+ +Mg 2+ ): Zr 4+ The example with a molar ratio of 5:95 was mixed evenly, dried and th...
Embodiment 2
[0037] Such as figure 1 As shown, first set Y 2 o 3 Dissolve with concentrated nitric acid to form 0.2mol?l -1 Stable and transparent Y(NO 3 ) 3 solution. Simultaneously ZrOCl 2 ·8H2 O is dissolved in distilled water to form 0.2mol?l -1 Stable clear solution. Then the two solutions according to (Y 3+ :Zr 4+ ) with a molar ratio of 8:92 for mixing and adding 4mol?l -1 KOH solution, adjust the pH value to 10 to form a uniform and stable co-precipitation product; then, the co-precipitation product is washed, dried at 90 ° C and heat-treated at 800 ° C for 1 h, and the precursor is obtained after natural cooling body. Then the precursor was mixed with 0.6mol?l -1 CaCl 2 -CaO composite molten salt (CaCl 2 / CaO molar ratio is 0.938:0.062) solution according to Ca 2+ :Zr 4+ The example with a molar ratio of 3:97 was mixed evenly, dried and then ground and passed through a 120-mesh sieve. It is pressed into a green body under a pressure system of 200Mpa and a holding ...
Embodiment 3
[0039] Such as figure 1 As shown, first set YC1 3 ·7H 2 O is dissolved in distilled water to form 0.2mol?l -1 Stable and transparent YCl 3 solution. At the same time, zirconium sulfate was dissolved in distilled water to form 0.2mol?l -1 Stable clear solution. Then the above two solutions according to (Y 3+ :Zr 4+ ) with a molar ratio of 10:90, and adjust the pH value to 7 with ammonia water. Add a slightly excess saturated urea solution and heat to 75°C, causing the solution to completely precipitate and form a uniform and stable co-precipitation product; then, wash the co-precipitation product, dry it at 90°C and dry it at 700°C The heat treatment was carried out for 1.5 h under the hood, and the precursor was obtained after natural cooling. Then the precursor was mixed with 0.6mol?l -1 BaCl 2 -CaCl 2 Composite molten salt (BaCl 2 / CaCl 2 Molar ratio is 0.359:0.641) solution according to (Ba 2+ +Ca 2+ ): Zr 4+ The example with a molar ratio of 3:97 was mixed...
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