Rare-earth perovskite type catalyst for purifying automobile tail gas and preparation method
A perovskite-type, automobile exhaust technology, which is applied in chemical instruments and methods, separation methods, and dispersed particle separation, can solve the problems of unsuitable purification of automobile exhaust and low activity, and achieve low cost, simple operation, and high activity. Effect
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Embodiment 1
[0019] Weigh 6.1g lanthanum nitrate (La(NO 3 ) 3 ·6H 2 O), 3.1g strontium nitrate (Sr(NO 3 ) 2 ), 3.6g manganese nitrate (Mn(NO 3 ) 2 4H 2 O), 2.5g citric acid (C 6 h 8 o 7 ·H 2 (0), it was dissolved in 70ml deionized water, stirred and dissolved at a temperature of 45° C. for 1 hour; the mixed solution was heated at a temperature of 120° C., and evaporated to dryness to obtain a catalyst precursor; The pre-calcined catalyst precursor was pre-calcined in a muffle furnace at a temperature program rate of ℃ / min, and the temperature was raised to 400 °C, kept at a constant temperature for 3.5 hours, and weighed to obtain 6.9 g of the precursor after cooling; the pre-calcined catalyst precursor was mixed with Add 0.2g of ground activated carbon powder, and press it into tablets with a pressure of 11 MPa; under the protection of nitrogen, calcinate the pressed catalyst at a programmed temperature increase rate of 11 °C / min, and the temperature rises to 1050 °C , constant...
Embodiment 2
[0024] Weigh 6.1g lanthanum nitrate (La(NO 3 ) 3 ·6H 2 O), 3.1g strontium nitrate (Sr(NO 3 ) 2 ), 3.6g manganese nitrate (Mn(NO 3 ) 2 4H 2 O), 2.3g citric acid (C 6 h 8 o 7 ·H 2 O), it was dissolved in 100ml deionized water, stirred and dissolved at a temperature of 50°C for 1.5 hours; the mixed solution was heated at a temperature of 110°C, and evaporated to dryness to obtain a catalyst precursor; The catalyst precursor was pre-calcined at a temperature programming rate of / min, and the temperature was raised to 400°C, kept at a constant temperature for 3 hours, and weighed to obtain 6.2g of the catalyst precursor after cooling; The final activated carbon carbon powder is compressed into tablets with a pressure of 10MPa; under the protection of nitrogen, the catalyst after the compression is calcined at a programmed temperature increase rate of 10°C / min, and the temperature rises to 1050°C, and the temperature is kept at a constant temperature for 4 hours. The cata...
Embodiment 3
[0027] Catalyst LaSrMnO 4 Preparation of:
[0028] Weigh 6.1g lanthanum nitrate (La(NO 3 ) 3 ·6H 2 O), 3.1g strontium nitrate (Sr(NO 3 ) 2 ), 3.6g manganese nitrate (Mn(NO 3 ) 2 4H 2 O), 2.5g citric acid (C 6 h 8 o 7 ·H 2 O), it was dissolved in 85ml deionized water, stirred and dissolved at a temperature of 55° C. for 1 hour; the mixed solution was heated at a temperature of 160° C., and evaporated to dryness to obtain a catalyst precursor; Pre-calcining the catalyst precursor at a temperature programming rate of / min, the temperature rose to 420°C, and weighed to obtain 7.1g of the precursor after cooling; 0.3g Printex-U carbon black was added to the pre-calcined catalyst precursor, It was pressed into tablets at a pressure of 10 MPa; under the protection of nitrogen, the compressed catalyst was calcined at a temperature program rate of 10 °C / min, the temperature was raised to 1000 °C, kept at a constant temperature for 4 hours, and the catalyst was obtained afte...
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