Ternary nano leadless piezoelectric ceramic material, and preparation method thereof
A ceramic material, lead-free piezoelectric technology, applied in the field of piezoelectric ceramic materials, can solve the problems of poor density of ceramic powder, low piezoelectric activity of product powder, low purity of ceramic powder, etc., to avoid Difficult polarization, excellent piezoelectric dielectric properties, and good compactness
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Embodiment 1
[0025] (1) Press (1-x) Bi 0.5 Na 0.5 TiO 3 -xBi 0.5 Na 0.5 NbO 3 +y Li proportioning, wherein x=0.4, y=0.006, weigh Ti(OC 4 h 9 ) 4 , Bi(NO 3 ) 3 ·5H 2 O, Nb 2 o 5 、CH 3 COOLi·2H 2 O, CH 3 COONa·3H 2 O and ethylene glycol ether;
[0026] (2) Bi(NO 3 ) 3 ·5H 2 O, CH 3 COONa·3H 2 O and CH 3 COOLi·2H 2 O was dissolved in an appropriate amount of glacial acetic acid, and then Ti(OC 4 h 9 ) 4 and a small amount of ethylene glycol ether, stirred at 60°C until the solution forms a uniform transparent sol;
[0027] (3) Nb 2 o 5 Slowly add the powder into the above sol, and continue to stir at 60°C to form a uniformly dispersed colloidal mixture;
[0028] (4) Let the above mixed solution stand for 12 hours, and after the colloid is fully matured, transfer it to a vacuum oven to dry at 100°C;
[0029] (5) heat-treat the dried product in a muffle furnace at 700°C for 2 hours, then take it out and grind it into powder;
[0030] (6) Use a powder tablet press ...
Embodiment 2
[0033] (1) Press (1-x) Bi 0.5 Na 0.5 TiO 3 -xBi0.5 Na 0.5 NbO 3 +y Mn proportioning, wherein x=0.4, y=0.004, weigh Ti(OC 4 h 9 ) 4 , Bi(NO 3 ) 3 ·5H 2 O, Nb 2 o 5 , Mn(CH 3 COO) 2 ·3H 2 O, CH 3 COONa·3H 2 O and ethylene glycol ether;
[0034] (2) Bi(NO 3 ) 3 ·5H 2 O, CH 3 COONa·3H 2 O and Mn(CH 3 COO) 2 ·3H 2 O was dissolved in an appropriate amount of glacial acetic acid, and then Ti(OC 4 h 9 ) 4 and a small amount of ethylene glycol ether, stirred at 60°C until the solution forms a uniform transparent sol;
[0035] (3) Nb 2 o 5 Slowly add the powder into the above sol, and continue to stir at 60°C to form a uniformly dispersed colloidal mixture;
[0036] (4) Let the above mixed solution stand for 12 hours, and after the colloid is fully matured, transfer it to a vacuum oven to dry at 100°C;
[0037] (5) heat-treat the dried product in a muffle furnace at 600°C for 2 hours, then take it out and grind it into powder;
[0038] (6) Use a powder ta...
Embodiment 3
[0041] (1)(1-x)Bi 0.5 Na 0.5 TiO 3 -xBi 0.5 Na 0.5 NbO 3 +y Zr proportioning, wherein x=0.6, y=0.008, weigh Ti(OC 4 h 9 ) 4 , Bi(NO 3 ) 3 ·5H 2 O, Nb 2 o 5 , Zr(NO 3 ) 4 ·5H 2 O, CH 3 COONa·3H 2 O and ethylene glycol ether;
[0042] (2) Bi(NO 3 ) 3 ·5H 2 O, CH 3 COONa·3H 2 O and Zr(NO 3 ) 4 ·5H 2 O was dissolved in an appropriate amount of glacial acetic acid, and then Ti(OC 4 h 9 ) 4 and a small amount of ethylene glycol ether, stirred at 60°C until the solution forms a uniform transparent sol;
[0043] (3) Nb 2 o 5 Slowly add the powder into the above sol, and continue to stir at 60°C to form a uniformly dispersed colloidal mixture;
[0044] (4) Let the above mixed solution stand for 12 hours, and after the colloid is fully matured, transfer it to a vacuum oven to dry at 100°C;
[0045] (5) heat-treat the dried product in a muffle furnace at 750°C for 2 hours, then take it out and grind it into powder;
[0046] (6) Use a powder tablet press t...
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