Catalytic cracking catalyst having a rare earth-containing Y zeolite and a preparation process thereof

US9656255B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9656255-B2
Application numberUS-201313929078-A
CountryUS
Kind codeB2
Filing dateJun 27, 2013
Priority dateSep 14, 2012
Publication dateMay 23, 2017
Grant dateMay 23, 2017

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  5. First independent claim

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Abstract

Official abstract text for this publication.

The present invention relates to a catalytic cracking catalyst and a preparation process thereof, the catalytic cracking catalyst has a cracking active component, an optional mesoporous aluminosilicate material, a clay and a binder, wherein said cracking active component comprises, substantially consists of or consists of: a rare earth-containing Y zeolite, an optional other Y zeolite, and an optional MFI-structured zeolite, said rare earth-containing Y zeolite has a rare earth content as rare earth oxide of 10-25 wt %, e.g. 11-23 wt %; a unit cell size of 2.440-2.472 nm, e.g. 2.450-2.470 nm; a crystallinity of 35-65%, e.g. 40-60%; a Si/Al atom ratio in the skeleton of 2.5-5.0; and a product of the ratio of the strength I 1 of the peak at 2θ=11.8±0.1° to the strength I 2 of the peak at 2θ=12.3±0.1° in the X-ray diffraction spectrogram of the zeolite and the weight percent of rare earth as rare earth oxide in the zeolite of higher than 48, e.g. higher than 55.

First claim

Opening claim text (preview).

What is claimed is: 1. A catalytic cracking catalyst, comprising a cracking active component, an optional mesoporous aluminosilicate material, a clay and a binder, wherein said cracking active component comprises a rare earth-containing Y zeolite, an optional other Y zeolite, and an optional MFI-structured zeolite, said rare earth-containing Y zeolite has a rare earth weight percent as rare earth oxide of 10-25 wt %; a unit cell size of 2.440-2.472 nm; a crystallinity of 35-65%; a Si/Al atom ratio in the skeleton of 2.5-5.0; and a product of the ratio of the strength I 1 of the peak at 2θ8=11.8±0.1° to the strength I 2 of the peak at 2θ8=12.3±0.1° in the X-ray diffraction spectrogram of the zeolite and the weight percent of rare earth as rare earth oxide in the zeolite of higher than 48. 2. The catalytic cracking catalyst according to claim 1 , wherein said rare earth-containing Y zeolite has a crystallinity retention after 17 hours of aging treatment at 800° C. in a condition of 100% steam of greater than 40%. 3. The catalytic cracking catalyst according to claim 1 , wherein said mesoporous aluminosilicate material has a pseudoboehmite phase structure, an anhydrous chemical expression formula based on the oxide weight ratio of (0-0.3)Na 2 O.(40-90)Al 2 O 3 .(10-60)SiO 2 , an average pore diameter of 5-25 nm, a specific surface area of 200-400 m 2 /g, and a pore volume of 0.5-2.0 ml/g; said clay is selected from the group consisting of kaolin, metahalloysite, montmorillonite, diatomite, halloysite, saponite, rectorite, sepiolite, attapulgite, hydrotalcite, bentonite and any mixture thereof; and said binder is selected from the group consisting of silica sol, alumina sol, pseudoboehmite and any mixture thereof. 4. The catalytic cracking catalyst according to claim 1 , wherein per 100 weight parts of the catalytic cracking catalyst, said catalytic cracking catalyst contains 10-60 weight parts of the cracking active component, 10-70 weight parts of the clay, 10-60 weights parts of the binder, and 0-20 weight parts of the mesoporous aluminosilicate material. 5. The catalytic cracking catalyst according to claim 1 , wherein said cracking active component comprises a rare earth-containing Y zeolite, an other Y zeolite, and an optional MFI-structured zeolite, further wherein said other Y zeolite is selected from the group consisting of rare earth-containing DASY zeolite, rare earth-containing gas-phase ultrastable Y zeolite and Mg-containing ultrastable Y zeolite. 6. The catalytic cracking catalyst according to claim 1 , wherein said cracking active component substantially consists of the rare earth-containing Y zeolite, optionally, a rare earth-containing DASY zeolite, and optionally, only one of a rare earth-containing gas-phase ultrastable Y zeolite, a Mg-containing ultrastable Y zeolite and the MFI-structured zeolite. 7. The catalytic cracking catalyst according to claim 1 , wherein per 100 weight parts of the catalytic cracking catalyst, said catalytic cracking catalyst contains 10-40 weight parts of the rare earth-containing Y zeolite, 0-15 weight parts of a rare earth-containing DASY zeolite, and 0-25 weight parts of only one of a rare earth-containing gas-phase ultrastable Y zeolite, a Mg-containing ultrastable Y zeolite and the MFI-structured zeolite. 8. The catalytic cracking catalyst according to claim 1 , wherein said rare earth-containing Y zeolite is prepared by a process comprising the following steps: (1) a NaY zeolite and a rare earth solution or a mixed solution of ammonium salt and rare earth solution are contacted to obtain a rare earth- and sodium-containing Y zeolite; (2) the rare earth- and sodium-containing Y zeolite obtained in step (1) is subjected to a first calcination to obtain a rare earth- and sodium-containing Y zeolite; (3) then either the rare earth- and sodium-containing Y zeolite obtained in step (2) is contacted with an ammonium salt solution or an acid solution, and then mixed with a rare earth solution, and the mixture is adjusted to a pH of 6-10, or the rare earth- and sodium-containing Y zeolite obtained in step (2) is contacted with a mixed solution of ammonium salt and rare earth solution, and then the mixture is adjusted to a pH of 6-10, to obtain a rare earth- and sodium-containing Y zeolite; (4) the rare earth- and sodium-containing Y zeolite obtained in step (3) is subjected to a second calcination to obtain the target rare earth-containing Y zeolite. 9. The catalytic cracking catalyst according to claim 1 , wherein said rare earth-containing Y zeolite is prepared by a process comprising the following steps: (1) a NaY zeolite and a rare earth solution or a mixed solution of ammonium salt and rare earth solution are contacted to obtain a rare earth- and sodium-containing Y zeolite; (2) the rare earth- and sodium-containing Y zeolite obtained in step (1), after being filtered and washed with water, and dried, is subjected to a first calcination to obtain a rare earth- and sodium-containing Y zeolite; (3) then either the rare earth- and sodium-containing Y zeolite obtained in step (2) is contacted with an ammonium salt solution, and then mixed with a rare earth solution without filtration, and the mixture is adjusted to a pH of 6-10, or the rare earth- and sodium-containing Y zeolite obtained in step (2) is contacted with a mixed solution of ammonium salt and rare earth solution, and then the mixture is adjusted to a pH of 6-10, to obtain a rare earth- and sodium-containing Y zeolite; (4) the rare earth- and sodium-containing Y zeolite obtained in step (3), after being filtered and washed with water, and dried, is subjected to a second calcination to obtain the target rare earth-containing Y zeolite. 10. The catalytic cracking catalyst according to claim 1 , wherein said rare earth-containing Y zeolite is prepared by a process comprising the following steps: (1) a NaY zeolite and a rare earth solution or a mixed solution of ammonium salt and rare earth solution are contacted to obtain a rare earth- and sodium-containing Y zeolite; (2) the rare earth- and sodium-containing Y zeolite obtained in step (1), after being filtered and washed with water, and dried, is subjected to a first calcination to obtain a rare earth- and sodium-containing Y zeolite; (3) the rare earth- and sodium-containing Y zeolite obtained in step (2) is contacted with an ammonium salt solution or an acid solution, filtered, and then mixed with a rare earth solution, and the mixture is adjusted to a pH of 6-10, to obtain a rare earth- and sodium-containing Y zeolite; (4) the rare earth- and sodium-containing Y zeolite obtained in step (3), after being optionally filtered and washed with water, and dried, is subjected to a second calcination to obtain the target rare earth-containing Y zeolite. 11. The catalytic cracking catalyst according to any one of claims 8 - 10 , wherein the ammonium salt is selected from the group consisting of ammonium chloride, ammonium nitrate, ammonium carbonate, ammonium hydrogen carbonate and any mixture thereof. 12. The catalytic cracking catalyst according to any one of claims 8 - 10 , wherein in step (1), the weight ratio of the rare earth solution (as rare earth oxide) to the NaY zeolite (on the dry basis) is 0.06-0.14, the weight ratio of the ammonium salt (as ammonium chloride) to the rare earth solution (as rare earth oxide) is 0-10, said ammonium salt is selected from the group consisting of ammonium chloride, ammonium nitrate, ammonium carbonate, ammonium hydrogen carbonate and any mixture thereof, the pH is adjusted to 3.0-5.0, the weight ratio of water:zeolite is controlled to 5-30, said contact is conducted at room temperatur

Assignees

Inventors

Classifications

  • Base treatment · CPC title

  • Y-type faujasite · CPC title

  • B01J29/084Primary

    Y-type faujasite · CPC title

  • Mesoporous materials not having base exchange properties, e.g. Si-MCM-41 · CPC title

  • B01J29/80Primary

    Mixtures of different zeolites · CPC title

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What does patent US9656255B2 cover?
The present invention relates to a catalytic cracking catalyst and a preparation process thereof, the catalytic cracking catalyst has a cracking active component, an optional mesoporous aluminosilicate material, a clay and a binder, wherein said cracking active component comprises, substantially consists of or consists of: a rare earth-containing Y zeolite, an optional other Y zeolite, and an o…
Who is the assignee on this patent?
China Petroleum & Chem Corp, Res Inst Petroleum Processing Sinopec
What technology area does this patent fall under?
Primary CPC classification B01J29/084. Mapped technology areas include Operations & Transport.
When was this patent published?
Publication date Tue May 23 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).