Low-temperature NO.SUB.x .storage catalyst used for automobile exhaust purification and preparation method thereof

Abstract

A low-temperature NO.sub.x storage catalyst for automobile exhaust purification and a preparation method thereof. Loading a noble metal salt solution on molecular sieve by equal volume impregnation method, wherein the noble metal salt solution comprises palladium nitrate and platinum nitrate, and the molecular sieve comprises SSZ, SAPO and BETA, then drying at 60-120° C. for 2-6 h, roasting at 500-550° C. in air for 2-5 h, and further roasting at 750-850° C. in air for 2-5 h, and then mixing with aluminum sol, ball milling and pulping, and then coating the slurry on a carrier, wherein the loading on the coating is 100-250 g/L and the noble metal content is 10-150 g/ft.sup.3, drying at 60-120° C. for 2-6 h, then roasting at 500-550° C. in air for 2-5 h, and further continuing roasting at 750-850° C. in air for 2-5 h, to obtain the catalyst. Loading the noble metals Pt and Pd into a pore channel of a molecular sieve improves NO.sub.x storage capacity of a catalyst at low temperatures, and selecting a different type of molecular sieve as an NO.sub.x storage unit and increasing a roasting temperature of a molecular sieve material on which Pt and Pd are loaded significantly increases NO.sub.x storage capacity.

Claims

1. A preparation method of low-temperature NO.sub.x storage catalyst for automobile exhaust purification, characterized by comprising the following steps: (1) Loading a noble metal salt solution on molecular sieve by equal volume impregnation method, wherein the noble metal salt solution comprises but not limited to palladium nitrate and platinum nitrate, and the molecular sieve comprises but not limited to SSZ, SAPO and BETA, and the content of noble metals in element accounts for more than 0% and no more than 3% by mass of the coating, then drying at 60-120° C. for 2-6 h, roasting at 500-550° C. in air for 2-5 h, and further roasting at 750-850° C. in air for 2-5 h to obtain M1; (2) Mixing M1 and aluminum sol, ball milling and pulping to obtain a noble metal slurry N1; (3) Coating the slurry N1 on a carrier, wherein the loading on the coating is 100-250 g/L and the noble metal content is 10-150 g/ft.sup.3, drying at 60-120° C. for 2-6 h, then roasting at 500-550° C. in air for 2-5 h, and further continuing roasting at 750-850° C. in air for 2-5 h, to obtain the catalyst.

2. The preparation method of low-temperature NO.sub.x storage catalyst for automobile exhaust purification according to claim 1, characterized in that, in step (1), the noble metal salt solution is a soluble salt solution of platinum and palladium.

3. The preparation method of low-temperature NO.sub.x storage catalyst for automobile exhaust purification according to claim 1, characterized in that, the mass ratio of platinum and palladium in the catalyst is 1:9-9:1.

4. The preparation method of low-temperature NO.sub.x storage catalyst for automobile exhaust purification according to claim 1, characterized in that, the molecular sieve is one of or a mixture of more of SSZ, SAPO or BETA.

5. A low-temperature NO.sub.x storage catalyst for automobile exhaust purification, characterized in that, the catalyst is a catalyst prepared by the preparation method of any one of claims 1 to 4.

Description

BRIEF DESCRIPTION OF THE FIGURES

(1) FIG. 1 shows the relative storage capacity of NO of the catalyst prepared in various examples of the present invention.

(2) In the figure, the ordinate is the relative adsorption amount of NO, in %; and on the abscissa, C0 is the comparative catalyst, and C1-C7 are the catalysts of Examples 1 to 7.

(3) FIG. 2 shows the relative storage capacity of NO of the catalysts prepared in Examples 6 and 8 of the present invention.

(4) In the figure, the ordinate is the relative storage amount of NO, in %; and on the abscissa, C6 is the catalyst of Example 6 and C8 is the catalyst of Example 8.

DETAILED DESCRIPTION OF EMBODIMENTS

(5) In the followings, the present invention will be further explained with reference to the specific examples, which are further explanations of the principle of the present invention and does not limit the present invention in any way. The same or similar technologies as the present invention do not exceed the scope of the present invention.

Comparative Example 1

(6) SAPO-34 was mixed with aluminum sol, ball-milled for 10 min, and the binder accounted for 3%, and the slurry N0 with a solid content of 45% was obtained.

(7) N0 was coated on cordierite substrate, and the carrier size was Φ25.4*101.6/400 cpsi-4 mil. The sample was dried at 80° C. for 6 h, roasted at 500° C. for 2 h, with a coating amount of 150 g/L.

(8) The catalyst prepared above was designated as C0.

Example 1

(9) Palladium nitrate solution was loaded on SAPO-34 molecular sieve by equal volume impregnation method, dried at 80° C. for 6 h, and roasted at 500° C. for 2 h, which was designated as M1.

(10) M1 is mixed with aluminum sol, ball-milled for 10 min, and the binder accounted for 3%, thus obtaining slurry N1 with a solid content of 45%.

(11) N1 was coated on cordierite substrate, and the carrier size was Φ25.4*101.6/400 cpsi-4 mil. The sample was dried at 80° C. for 6 h, roasted at 500° C. for 2 h, with a coating amount of 150 g/L, a noble metal content of 100 g/ft.sup.3.

(12) The catalyst prepared above was designated as C1.

Example 2

(13) Platinum nitrate solution was loaded on SAPO-34 molecular sieve by equal volume impregnation method, dried at 80° C. for 6 h, and roasted at 500° C. for 2 h, which was designated as M2.

(14) M2 was mixed with aluminum sol, ball-milled for 10 min, and the binder accounted for 3%, thus obtaining slurry N2 with a solid content of 45%.

(15) N2 was coated on cordierite substrate, and the carrier size was Φ25.4*101.6/400 cpsi-4 mil. The sample was dried at 80° C. for 6 h, roasted at 500° C. for 2 h, with a coating amount of 150 g/L, a noble metal content of 100 g/ft.sup.3.

(16) The catalyst prepared above was designated as C2.

Example 3

(17) Platinum nitrate solution was loaded on SAPO-34 molecular sieve by equal volume impregnation method, dried at 80° C. for 6 h and roasted at 500° C. for 2 h, which was designated as M3-1.

(18) Palladium nitrate solution was loaded on SAPO-34 molecular sieve by equal volume impregnation method, dried at 80° C. for 6 h, and roasted at 500° C. for 2 h, which was designated as M3-2.

(19) M3-1 and M3-2 were mixed at a ratio of 1:3, and aluminum sol was added. After ball milling for 10 min, the binder accounted for 3%, and the slurry N3 with a solid content of 45% was obtained.

(20) N3 was coated on cordierite substrate, and the carrier size was Φ25.4*101.6/400 cpsi-4 mil. The sample was dried at 80° C. for 6 h, roasted at 500° C. for 2 h, with a coating amount of 150 g/L, a noble metal content of 100 g/ft.sup.3.

(21) The catalyst prepared above was designated as C3.

Example 4

(22) Platinum nitrate solution was loaded on SAPO-34 molecular sieve by equal volume impregnation method, dried at 80° C. for 6 h and roasted at 500° C. for 2 h, which was designated as M4-1.

(23) Palladium nitrate solution was loaded on SAPO-34 molecular sieve by equal volume impregnation method, dried at 80° C. for 6 h, and roasted at 500° C. for 2 h, which was designated as M4-2.

(24) M4-1 and M4-2 were mixed in a ratio of 3:1, and aluminum sol was added. After ball milling for 10 min, the binder accounted for 3%, and the slurry N4 with a solid content of 45% was obtained.

(25) N4 was coated on cordierite substrate, and the carrier size was Φ25.4*101.6/400 cpsi-4 mil. The sample was dried at 80° C. for 6 h, roasted at 500° C. for 2 h, with a coating amount of 150 g/L, a noble metal content of 100 g/ft.sup.3.

(26) The catalyst prepared above was designated as C4.

Example 5

(27) Platinum nitrate solution was loaded on SAPO-34 molecular sieve by equal volume impregnation method, dried at 80° C. for 6 h and roasted at 500° C. for 2 h, which was designated as M5-1.

(28) Palladium nitrate solution was loaded on SAPO-34 molecular sieve by equal volume impregnation method, dried at 80° C. for 6 h, and roasted at 500° C. for 2 h, which was designated as M5-2.

(29) M5-1 and M5-2 were mixed at a ratio of 1:1, and aluminum sol was added. After ball milling for 10 min, the binder accounted for 3%, and the slurry N5 with a solid content of 45% was obtained.

(30) N5 was coated on cordierite substrate, and the carrier size was Φ25.4*101.6/400 cpsi-4 mil. The sample was dried at 80° C. for 6 h, roasted at 500° C. for 2 h, with a coating amount of 150 g/L, a noble metal content of 100 g/ft.sup.3.

(31) The catalyst prepared above was designated as C5.

Example 6

(32) Platinum nitrate solution was loaded on SSZ-13 molecular sieve by equal volume impregnation method, dried at 80° C. for 6 h and roasted at 500° C. for 2 h, which was designated as M6-1.

(33) Palladium nitrate solution was loaded on SSZ-13 molecular sieve by equal volume impregnation method, dried at 80° C. for 6 h and roasted at 500° C. for 2 h, which was designated as M6-2.

(34) M6-1 and M6-2 were mixed in a ratio of 3:1, and aluminum sol was added. After ball milling for 10 min, the binder accounted for 3%, and the slurry N6 with a solid content of 45% was obtained.

(35) N6 was coated on cordierite substrate, and the carrier size was Φ25.4*101.6/400 cpsi-4 mil. The sample was dried at 80° C. for 6 h, roasted at 500° C. for 2 h, with a coating amount of 150 g/L, a noble metal content of 100 g/ft.sup.3.

(36) The catalyst prepared above was designated as C6.

Example 7

(37) Platinum nitrate solution was loaded on BETA molecular sieve by equal volume impregnation method, dried at 80° C. for 6 h, and roasted at 500° C. for 2 h, which was designated M7-1.

(38) Palladium nitrate solution was loaded on BETA molecular sieve by equal volume impregnation method, dried at 80° C. for 6 h, and roasted at 500° C. for 2 h, which was designated as M7-2.

(39) M7-1 and M7-2 were mixed in a ratio of 3:1, and aluminum sol was added. After ball milling for 10 min, the binder accounted for 3%, and the slurry N7 with a solid content of 45% was obtained.

(40) N7 was coated on cordierite substrate, and the carrier size was Φ25.4*101.6/400 cpsi-4 mil. The sample was dried at 80° C. for 6 h, roasted at 500° C. for 2 h, with a coating amount of 150 g/L, a noble metal content of 100 g/ft.sup.3.

(41) The catalyst prepared above was designated as C7.

Example 8

(42) Platinum nitrate solution was loaded on SSZ-13 molecular sieve by equal volume impregnation method, dried at 80° C. for 6 h, roasted at 500° C. for 2 h and roasted at 800° C. for 2 h, which was designated as M8-1.

(43) Palladium nitrate solution was loaded on SSZ-13 molecular sieve by equal volume impregnation method, dried at 80° C. for 6 h, roasted at 500° C. for 2 h and roasted at 800° C. for 2 h, which was designated as M8-2.

(44) M6-1 and M6-2 were mixed in a ratio of 3:1, and aluminum sol was added. After ball milling for 10 min, the binder accounted for 3%, and the slurry N8 with a solid content of 45% was obtained.

(45) N8 was coated on cordierite substrate, and the carrier size was Φ25.4*101.6/400 cpsi-4 mil. The sample was dried at 80° C. for 6 h, roasted at 500° C. for 2 h and roasting at 800° C. for 2 h, with a coating amount of 150 g/L, a noble metal content of 100 g/ft.sup.3.

(46) The catalyst prepared above was designated as C8.

(47) The catalysts prepared in the above examples were tested for activity evaluation under the following test conditions.

(48) The temperature of the catalyst was programmatically elevated to 450° C. in 5% O.sub.2 atmosphere, kept at constant temperature for 1 hour, cooled to 25° C., and the experimental atmosphere was switched to 5% NO, kept at constant temperature for 30 min, then switched to N.sub.2, and the temperature was increased to 450° C. at 10° C./min. In the test, NO was used to replace NO.sub.x in the exhaust emission. The relative adsorption amount of NO in each Example and Comparative Example is shown in FIG. 1.

(49) As can be seen from FIG. 1:

(50) 1) Compared with Comparative Example C0, Examples C1 and C2 have the same molecular sieve. Comparative Example C0 does not contain noble metals, and C1 and C2 are loaded with noble metals Pd and Pt respectively. The relative adsorption capacity of NO increased greatly after Loading a noble metals in molecular sieves.

(51) 2) In Examples C1-C5, the molecular sieves were the same, but the noble metals and proportions were different. Compared with C1, C2 had a higher adsorption capacity of NO, such that Pt, as an active component, had a higher adsorption capacity of NO than Pd. C3-C5 were catalysts with different ratios of Pt and Pd, and the tendencies were the same as those of C1 and C2. C2 and C4 with higher Pt content had relatively higher adsorption capacity.

(52) 3) In Example C6, compared with C4, noble metals and proportions were the same, but molecular sieves were different. Compared with C4, C6 molecular sieve changed from SAPO-34 to SSZ-13, and the relative adsorption capacity of NO increased.

(53) 4) In Example C7, compared with C4, noble metals and proportions were the same, but molecular sieves were different. Compared with C4, C7 molecular sieve changed from SAPO-34 to BETA, the relative adsorption capacity of NO decreased.

(54) 5) In Example C8, compared with C6, the noble metals and proportions were the same, and the molecular sieve was the same. The main difference was the roasting temperature of molecular sieve powder supported by noble metals. Compared with C6, C8 powders, when the roasting temperature was increased from 500° C. to 800° C., the relative NO adsorption capacity of the prepared catalyst was further significantly improved.

(55) The above experiments show that, (a) the storage capacity of NO is greatly increased after noble metals are loaded in molecular sieves; and (b) when loaded on molecular sieve, compared with Pd, the storage capacity of NO is relatively larger for noble metal Pt; and (c) under the premise of loading the same noble metals, the storage capacity of NO by BETA, SAPO-34 and SSZ-13 molecular sieves increases in turn; and (d) increasing the roasting temperature of the noble metal-loaded molecular sieve results in further increasing the NO storage capacity.