RU2008128363A - ЦЕОЛИТНЫЙ КАТАЛИЗАТОР С УЛУЧШЕННЫМ ВОССТАНОВЛЕНИЕМ NOх В SCR - Google Patents
ЦЕОЛИТНЫЙ КАТАЛИЗАТОР С УЛУЧШЕННЫМ ВОССТАНОВЛЕНИЕМ NOх В SCR Download PDFInfo
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- RU2008128363A RU2008128363A RU2008128363/15A RU2008128363A RU2008128363A RU 2008128363 A RU2008128363 A RU 2008128363A RU 2008128363/15 A RU2008128363/15 A RU 2008128363/15A RU 2008128363 A RU2008128363 A RU 2008128363A RU 2008128363 A RU2008128363 A RU 2008128363A
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- zeolite
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- zeolite catalyst
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- B01J29/10—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the faujasite type, e.g. type X or Y containing iron group metals, noble metals or copper
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- Exhaust Gas After Treatment (AREA)
Abstract
1. Способ получения нового металл-промотированного цеолитного катализатора для селективного каталитического восстановления NOx, упомянутый катализатор синтезируют способом, включающим стадии: ! - ионообмен упомянутого металла в цеолит, ! - последующее обрабатывание упомянутого металлобмененного цеолита гидротермальной обработкой, и ! - где упомянутый катализатор имеет улучшенную активность восстановления NOx в селективном каталитическом восстановлении по сравнению с металл-обмененным цеолитным катализатором не обработанным стадией б. ! 2. Способ по п.1, в котором упомянутый цеолит выбирают из группы, включающей цеолит Y, фоязиты, ультрастабильный Y, ZSM-3, ZSM-20, CSZ-1, ECR-30, LZ-210, цеолит L, ферриерит, МСМ-22 и оффретит, и в котором упомянутый металл выбирают из группы, включающей ионы металла ванадия, хрома, марганца, железа, кобальта, никеля, меди и церия. ! 3. Способ по п.1, в котором упомянутый ионный обмен металла проходит в водном обменном растворе с рН от приблизительно 2.5 до приблизительно 3.5. ! 4. Способ по п.1, в котором упомянутый металлобмененный цеолит гидротермально обрабатывают при температуре от приблизительно 540 до приблизительно 1000°С, паром с концентрацией от приблизительно 5 до приблизительно 100%, на протяжении от приблизительно 5 мин до приблизительно 250 ч. ! 5. Медь содержащий алюмосиликатный цеолитный катализатор образованный способом по п.1. ! 6. Гидротермально стабильный цеолитный катализатор для селективного восстановления оксидов азота, упомянутый катализатор, включает: металл-промотированный цеолитный катализатор, в котором упомянутый металл-промотированный цеолит должен быть обработан, чтобы образовать ал�
Claims (10)
1. Способ получения нового металл-промотированного цеолитного катализатора для селективного каталитического восстановления NOx, упомянутый катализатор синтезируют способом, включающим стадии:
- ионообмен упомянутого металла в цеолит,
- последующее обрабатывание упомянутого металлобмененного цеолита гидротермальной обработкой, и
- где упомянутый катализатор имеет улучшенную активность восстановления NOx в селективном каталитическом восстановлении по сравнению с металл-обмененным цеолитным катализатором не обработанным стадией б.
2. Способ по п.1, в котором упомянутый цеолит выбирают из группы, включающей цеолит Y, фоязиты, ультрастабильный Y, ZSM-3, ZSM-20, CSZ-1, ECR-30, LZ-210, цеолит L, ферриерит, МСМ-22 и оффретит, и в котором упомянутый металл выбирают из группы, включающей ионы металла ванадия, хрома, марганца, железа, кобальта, никеля, меди и церия.
3. Способ по п.1, в котором упомянутый ионный обмен металла проходит в водном обменном растворе с рН от приблизительно 2.5 до приблизительно 3.5.
4. Способ по п.1, в котором упомянутый металлобмененный цеолит гидротермально обрабатывают при температуре от приблизительно 540 до приблизительно 1000°С, паром с концентрацией от приблизительно 5 до приблизительно 100%, на протяжении от приблизительно 5 мин до приблизительно 250 ч.
5. Медь содержащий алюмосиликатный цеолитный катализатор образованный способом по п.1.
6. Гидротермально стабильный цеолитный катализатор для селективного восстановления оксидов азота, упомянутый катализатор, включает: металл-промотированный цеолитный катализатор, в котором упомянутый металл-промотированный цеолит должен быть обработан, чтобы образовать алюминий экстра-основы и в котором значительная часть упомянутого алюминия экстра-основы удаляется из цеолитных пор.
7. Цеолитный катализатор по п.6, в котором меньше чем 65 маc. % общего алюминия находится в цеолитных порах.
8. Металл-промотированный цеолитный катализатор по п.6, в котором упомянутый цеолит представляет собой цеолит Y и упомянутый металл представляет собой медь.
9. Металл-промотированный цеолитный катализатор по п.6, в котором цеолит содержит мезопоры с диаметром 2 - 50 нм и упомянутые мезопоры имеют объем пор по меньшей мере 0.07 см3/г.
10. Способ восстановления NOx в потоке выхлопного газа или топочного газа аммиаком и кислородом при помощи селективного каталитического восстановления упомянутым способом, включающим контактирование упомянутого потока выхлопного газа или топочного газа с металл-промотированным цеолитным катализатором по п.1 или 6.
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| US60/750,261 | 2005-12-14 | ||
| US11/639,182 US7704475B2 (en) | 2005-12-14 | 2006-12-14 | Zeolite catalyst with improved NOx reduction in SCR |
| US11/639,182 | 2006-12-14 |
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| RU2008128363A true RU2008128363A (ru) | 2010-01-20 |
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| RU2008128363/15A RU2008128363A (ru) | 2005-12-14 | 2006-12-14 | ЦЕОЛИТНЫЙ КАТАЛИЗАТОР С УЛУЧШЕННЫМ ВОССТАНОВЛЕНИЕМ NOх В SCR |
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| RU (1) | RU2008128363A (ru) |
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| DE4003515A1 (de) | 1990-02-06 | 1991-08-08 | Bayer Ag | Verfahren zur reduktion von in abgasen enthaltenen stickoxiden |
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| EP1973633A2 (en) | 2005-12-14 | 2008-10-01 | BASF Catalysts LLC | Zeolite catalyst with improved nox reduction in scr |
-
2006
- 2006-12-14 EP EP06845422A patent/EP1973633A2/en not_active Ceased
- 2006-12-14 CN CNA200680051790XA patent/CN101336129A/zh active Pending
- 2006-12-14 RU RU2008128363/15A patent/RU2008128363A/ru not_active Application Discontinuation
- 2006-12-14 BR BRPI0619944A patent/BRPI0619944B8/pt not_active IP Right Cessation
- 2006-12-14 WO PCT/US2006/047711 patent/WO2007070639A2/en not_active Ceased
- 2006-12-14 KR KR1020087016846A patent/KR101394774B1/ko not_active Expired - Fee Related
- 2006-12-14 US US11/639,182 patent/US7704475B2/en not_active Expired - Fee Related
- 2006-12-14 JP JP2008545808A patent/JP5261189B2/ja not_active Expired - Fee Related
-
2008
- 2008-07-10 ZA ZA200806013A patent/ZA200806013B/xx unknown
-
2010
- 2010-01-13 US US12/686,663 patent/US7968068B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| WO2007070639A2 (en) | 2007-06-21 |
| WO2007070639A3 (en) | 2007-09-20 |
| US20100172814A1 (en) | 2010-07-08 |
| BRPI0619944A2 (pt) | 2011-10-25 |
| BRPI0619944B8 (pt) | 2018-03-20 |
| JP5261189B2 (ja) | 2013-08-14 |
| EP1973633A2 (en) | 2008-10-01 |
| CN101336129A (zh) | 2008-12-31 |
| US7968068B2 (en) | 2011-06-28 |
| ZA200806013B (en) | 2009-10-28 |
| US20070134146A1 (en) | 2007-06-14 |
| JP2009519817A (ja) | 2009-05-21 |
| BRPI0619944B1 (pt) | 2018-02-27 |
| KR101394774B1 (ko) | 2014-05-15 |
| WO2007070639A8 (en) | 2007-08-02 |
| KR20080081031A (ko) | 2008-09-05 |
| US7704475B2 (en) | 2010-04-27 |
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