A dual-phase ceramic material of homologous double perovskite and its preparation method and application
A ceramic material, double perovskite technology, applied in the application field of hydrogen separation materials, can solve the problems of high tension of materials, difficult to meet application conditions, unable to operate stably, and achieve the effect of low cost and simple process
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Embodiment 1
[0042] A preparation method of a homologous double perovskite dual-phase ceramic material, specifically comprising the following steps:
[0043] (1) 12.47g SrCO 3 , 11.63 g CeO 2 and 1.91g Y 2 o 3 Dissolve in 25ml of acetone, ball mill at 800r / min for 24h, and then stand at 60°C for 14h to obtain the proton conductive phase SrCe 0.8 Y 0.2 o 3-δ The precursor of the powder; the precursor is placed in a muffle furnace and raised to 1000°C at a heating rate of 2°C / min, kept for 10 hours, and then lowered to room temperature at a cooling rate of 2°C / min to obtain the protons of the perovskite conductive phase;
[0044] (2) 10.59g SrCO 3 , 1.23g CeO 2 and 12.72g Yb 2 o 3 Dissolve in 25ml of acetone, ball mill at 800r / min for 24 hours, and then stand at 60°C for 14 hours to obtain the electronically conductive phase SrCe 0.1 Yb 0.9 o 3-δ The precursor of the powder; the precursor is placed in a muffle furnace and raised to 1000°C at a heating rate of 2°C / min, kept for 1...
Embodiment 2
[0055] A preparation method of a homologous double perovskite dual-phase ceramic material, specifically comprising the following steps:
[0056] (1) 15.56g BaCO 3 , 10.85g CeO 2 and 3.02g Er 2 o 3 Dissolve in 25ml of acetone, ball mill at 400r / min for 24h, and then stand at 80°C for 10h to obtain the proton conductive phase BaCe 0.8 Er 0.2 o 3-δ The precursor of the powder; the precursor is placed in a muffle furnace and raised to 1200°C at a heating rate of 2°C / min, kept for 10 hours, and then lowered to room temperature at a cooling rate of 2°C / min to obtain the protons of the perovskite conductive phase;
[0057] (2) 14.59g BaCO 3 , 2.55g CeO 2 and 10.31g Sm 2 o 3 Dissolve in 25ml of acetone, ball mill at 400r / min for 24h, and then stand at 80°C for 10h to obtain the electronically conductive phase BaCe 0.2 SM 0.8 o 3-δ The precursor of the powder; the precursor is placed in a muffle furnace and raised to 1200°C at a heating rate of 2°C / min, kept for 10 hours, ...
Embodiment 3
[0064] A preparation method of a homologous double perovskite dual-phase ceramic material, specifically comprising the following steps:
[0065] (1) 9.56g SrCO 3 , 10.59 g CeO 2 and 0.57g Eu 2 o 3 Dissolve in 20ml of acetone, ball mill at 800r / min for 24h, and then stand at 80°C for 10h to obtain the proton conductive phase SrCe 0.95 Eu 0.05 o 3-δ The precursor of the powder; the precursor is placed in a muffle furnace and raised to 900°C at a heating rate of 2°C / min, kept for 10 hours, and then lowered to room temperature at a cooling rate of 2°C / min to obtain the protons of the perovskite conductive phase;
[0066] (2) 10.59g SrCO 3 , 1.23g CeO 2 and 12.72g Yb 2 o 3 Dissolve in 20ml of acetone, ball mill at 800r / min for 24h, and then stand at 80°C for 10h to obtain the electronically conductive phase SrCe 0.1 Yb 0.9 o 3-δ The precursor of the powder; the precursor is placed in a muffle furnace and raised to 900°C at a heating rate of 2°C / min, kept for 15 hours, ...
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Abstract
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