Negative thermal expansion ceramic material Sc<x>In<2-x>Mo<3>O<12> and method for preparing same
A technology of scxin2-xmo3o12 and scxin2-mox3o12, which is applied in the field of negative thermal expansion inorganic functional ceramic materials, can solve the problems of unfavorable application and achieve the effect of compact ceramic structure, wide application value and application prospect, and stable thermal expansion performance
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Embodiment 1
[0024] (1) Synthesis of negative thermal expansion material Sc1.4 In 0.6 Mo 3 o 12 , to analyze pure Sc 2 o 3 、In 2 o 3 and MoO 3 Powder is raw material, according to molar ratio Sc 2 o 3 : In 2 o 3 :MoO 3 =0.7:0.3:3 Weigh the raw materials, and after mixing, ball mill them in deionized water for 3 hours, dry the mixed raw materials after ball milling in an oven at 120°C, put the raw materials in an agate mortar, mix and grind them for 2 hours;
[0025] (2) Add polyvinyl alcohol accounting for 1% of the total mass of the precursor to the homogeneously ground material in step (1), grind for 40 minutes and mix evenly, and then cold isostatically press at 50 MPa to form a tablet;
[0026] (3) Place the material after tableting in step (2) in a furnace for debinding at 500°C for 2 hours, sinter at 750°C for 6 hours, and obtain pre-fired negative thermal expansion ceramic material Sc after cooling in the furnace 1.4 In 0.6 Mo 3 o 12 .
[0027] (4) the negative therm...
Embodiment 2
[0029] (1) Synthesis of negative thermal expansion material Sc 1.5 In 0.5 Mo 3 o 12 , to analyze pure Sc 2 o 3 、In 2 o 3 and MoO 3 Powder is raw material, according to molar ratio Sc 2 o 3 : In 2 o 3 :MoO 3 = 0.75: 0.25: 3 Weigh the raw materials, ball mill them in deionized water for 4 hours after mixing, dry the mixed raw materials in an oven at 130°C, put the raw materials in an agate mortar, mix and grind them for 1.5 hours;
[0030] (2) Add polyvinyl alcohol accounting for 2% of the total mass of the precursor to the homogeneously ground material in step (1), grind for 30 minutes and mix evenly, and then cold isostatically press at 40 MPa to form a tablet;
[0031] (3) Place the material after tableting in step (2) in a furnace for debinding at 500°C for 1.5 hours, sinter at 700°C for 9 hours, and obtain a pre-fired negative thermal expansion ceramic material Sc after cooling in the furnace 1.5 In 0.5 Mo 3 o 12 .
[0032] (4) the negative thermal expansio...
Embodiment 3
[0034] (1) Synthesis of negative thermal expansion material Sc 1.6 In 0.4 Mo 3 o 12 , to analyze pure Sc 2 o 3 、In 2 o 3 and MoO 3 Powder is raw material, according to molar ratio Sc 2 o 3 :In 2 o 3 :MoO 3 =0.8:0.2:3 Weigh the raw materials, and ball mill them in deionized water for 6 hours after mixing, dry the mixed raw materials in an oven at 150°C, put the raw materials in an agate mortar, mix and grind for 1 hour;
[0035] (2) Add polyvinyl alcohol accounting for 3% of the total mass of the precursor to the homogeneously ground material in step (1), grind for 20 minutes and mix evenly, and then cold isostatically press at 25 MPa to form a tablet;
[0036] (3) Place the material after tableting in step (2) in a furnace for debinding at 500°C for 1 hour, sinter at 650°C for 12 hours, and obtain a pre-fired negative thermal expansion ceramic material Sc after cooling in the furnace 1.6 In 0.4 Mo 3 o 12 .
[0037] (4) the negative thermal expansion ceramic ma...
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