US2019015783A1PendingUtilityA1
Methods Utilizing Non-Zeolitic Metal-Containing Molecular Sieves Having The CHA Crystal Structure
Est. expiryJan 31, 2028(~1.5 yrs left)· nominal 20-yr term from priority
B01D 53/9418F01N 3/2066B01D 2255/20715B01D 2255/1021B01D 2251/2067B01J 29/005B01J 2229/186F01N 2610/02B01D 2251/2062B01D 2255/9207Y02C20/10B01D 2255/20761B01D 53/9477F01N 2610/08B01D 2255/50B01D 2255/915B01J 37/0246B01D 2255/504B01J 29/85B01D 2255/502B01D 53/945B01D 2255/20738B01J 35/04Y02T10/22Y02T10/24B01J 35/56Y02T10/12B01J 35/615B01J 35/617
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Claims
Abstract
Catalysts comprising metal-loaded non-zeolitic molecular sieves having the CHA crystal structure, including Cu-SAPO-34, and methods for treating exhaust gas incorporating such catalysts are disclosed. The catalysts can be used to remove nitrogen oxides from a gaseous medium across a broad temperature range and exhibit hydrothermal stability at high reaction temperatures.
Claims
exact text as granted — not AI-modified1 - 19 . (canceled)
20 . A catalyst comprising:
an ion-exchanged Cu-SAPO-34 non-zeolitic molecular sieve having a CHA crystal structure; wherein the Cu content of the Cu-SAPO-34 non-zeolitic molecular sieve on a CuO basis is in the range of about 1% to about 5% by weight; wherein the Cu-SAPO-34 non-zeolitic molecular sieve has a BET surface area greater than 350 m 2 /g; wherein the catalyst is effective to promote the reaction of ammonia with nitrogen oxides (NOx) to form nitrogen and H 2 O selectively in an exhaust gas stream at 200° C. when the catalyst has been deposited on a honeycomb substrate having a cell density of 400 cpsi at a loading between 2 and 2.5 g/in 3 and tested at a space velocity of 80,000 hr −1 where the feed stream comprises a mixture of 10% O 2 , 5% H 2 O, 500 ppm NO and 500 ppm NH 3 to provide at least 80% NOx conversion; and wherein the catalyst is effective to make less than 5 ppm N 2 O over a temperature range of 200° C. to 450° C.
21 . The catalyst of claim 20 , wherein the Cu-SAPO-34 non-zeolitic molecular sieve has a BET surface area in the range of 375 m 2 /g to 600 m 2 /g.
22 . The catalyst of claim 20 , wherein the Cu-SAPO-34 non-zeolitic molecular sieve contains a secondary metal.
23 . The catalyst of claim 22 , wherein the secondary metal comprises zirconium.
24 . The catalyst of claim 20 , wherein the Cu content of the Cu-SAPO-34 non-zeolitic molecular sieve on a CuO basis is in the range of about 2% to 4 by weight.
25 . The catalyst of claim 20 , wherein the catalyst is effective to provide at least about 85% NOx conversion in the exhaust gas stream at 200° C.
26 . The catalyst of claim 20 , wherein the catalyst is effective to provide at least about 90% NOx conversion in the exhaust gas stream at 200° C.
27 . The catalyst of claim 20 , wherein the Cu-SAPO-34 non-zeolitic molecular sieve, upon hydrothermal aging in 10% steam at 850° C. for 6 hours, retains at least 85% on a percentage basis of the NOx conversion at 200° C.
28 . The catalyst of claim 20 , wherein the Cu-SAPO-34 non-zeolitic molecular sieve, upon hydrothermal aging in 10% steam at 900° C. and 1 hour, retains at least 90% of the NOx conversion on a percentage basis at 200° C.
29 . The catalyst of claim 20 , wherein the Cu-SAPO-34 non-zeolitic molecular sieve, upon hydrothermal aging in 10% steam at 900° C. and 1 hour, retains at least 95% of the NOx conversion on a percentage basis at 200° C.
30 . The catalyst of claim 20 , wherein the catalyst is effective to reduce NOx so that the exhaust gas stream contains a ratio of NOx to N 2 O after passing through the catalyst of greater than 2.5
31 . The catalyst of claim 20 , wherein the catalyst is effective to reduce NOx so that the exhaust gas stream contains a ratio of NOx to N 2 O after passing through the catalyst of greater than 5.
32 . The catalyst of claim 20 , wherein the Cu-SAPO-34 non-zeolitic molecular sieve is combined with a metal-containing zeolitic SCR catalyst.
33 . The catalyst of claim 32 , wherein the metal-containing zeolitic SCR catalyst comprises a zeolite selected from beta zeolite, zeolite Y, and ZSM-5.
34 . The catalyst of claim 32 , wherein the metal-containing zeolitic SCR catalyst comprises FeBeta.
35 . The catalyst of claim 32 , wherein the Cu-SAPO-34 non-zeolitic molecular sieve is physically mixed with the metal-containing zeolitic SCR catalyst.
36 . A catalyst composite comprising the catalyst of claim 20 deposited on a honeycomb substrate as a washcoat at a loading in the range of about 0.5 g/in 3 to 3.5 g/in 3 .
37 . The catalyst composite of claim 36 , wherein the Cu-SAPO-34 non-zeolitic molecular sieve is in a separate washcoat from the metal-containing zeolitic SCR catalyst.
38 . The catalyst composite of claim 36 , wherein the honeycomb substrate comprises a wall-flow substrate.
39 . The catalyst composite of claim 36 , wherein the honeycomb substrate comprises a flow-through substrate.
40 . The catalyst composite of claim 38 , wherein at least a portion of the wall-flow substrate is coated with a washcoat containing Pt and a metal-loaded non-zeolitic molecular sieve to oxidize ammonia in the exhaust gas stream.
41 . The catalyst composite of claim 39 , wherein at least a portion of the flow-through substrate is coated with a washcoat containing Pt and a metal-loaded non-zeolitic molecular sieve to oxidize ammonia in the exhaust gas stream.
42 . An exhaust gas treatment system comprising an oxidation catalyst and the catalyst composite of claim 36 .Join the waitlist — get patent alerts
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