US2003173254A1PendingUtilityA1
Catalytic cracking with zeolite ITQ-13
Priority: Mar 12, 2002Filed: Nov 4, 2002Published: Sep 18, 2003
Est. expiryMar 12, 2022(expired)· nominal 20-yr term from priority
C10G 2400/20B01J 29/86C10G 11/05G09F 11/00B01J 29/70
40
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Claims
Abstract
A catalytic cracking process is disclosed for feedstock containing hydrocarbons having at least 5 carbon atoms. The feedstock is contacted, under catalytic cracking conditions, with a 9-member ring catalyst composition and, optionally, a large pore molecular sieve, such as zeolite Y.
Claims
exact text as granted — not AI-modifiedWe claim:
1 . A catalytic cracking process comprising contacting, under catalytic cracking conditions, a feedstock comprising hydrocarbons having at least 5 carbon atoms with a catalyst composition comprising a synthetic porous crystalline material having a multi-dimensional channel system, at least a first parallel set of said channels comprising 9-member rings having a pore size of at least about 3.6 Angstroms.
2 . The process of claim 1 , wherein at least a second set of said channels comprises 10-member rings.
3 . The process of claim 1 , wherein the catalyst channel system is 3-dimensional.
4 . The process of claim 1 , wherein said at least first parallel set of channels has a pore size of at least about 4.0 Angstroms.
5 . The process of claim 1 , wherein said at least first parallel set of channels has a pore size of at least about 4.2 Angstroms.
6 . The process of claim 4 , wherein said at least first parallel set of channels has a pore size less than or equal to about 5.0 Angstroms.
7 . The process of claim 5 , wherein said at least first parallel set of channels has a pore size less than or equal to about 5.0 Angstroms.
8 . The process of claim 1 , wherein the catalyst is metal-stabilized.
9 . The process of claim 8 , wherein the catalyst is metal-stabilized with at least one of at least one metal of Group 2a, 3b, 4b, 7b, 8, 1b, 2b, 3a and 5a of The Periodic Table of the Elements.
10 . The process of claim 9 , wherein the catalyst is metal-stabilized with at least one of copper, phosphorus, iron, silver, magnesium, lanthanum, zinc, aluminum, zirconium, manganese, and cerium.
11 . The process of claim 10 , wherein the catalyst is metal stabilized with at least one of copper and phosphorous.
12 . The process of claim 1 , wherein the feedstock is naphtha.
13 . The process of claim 1 , wherein the feedstock is at least one of gas oil, vacuum gas oil and residual oil vacuum resid.
14 . The process of claim 1 , which is a fluid catalytic cracking process.
15 . The process of claim 1 , wherein the catalyst composition is used as an additive catalyst.
16 . The process of claim 1 , wherein the catalyst composition is used as a base catalyst.
17 . The process of claim 1 , wherein the catalyst composition comprises a molecular sieve.
18 . The process of claim 17 , wherein the catalyst comprises at least one of zeolite Y, zeolite REY, zeolite X, zeolite USY and zeolite REUSY.
19 . The process of claim 1 , wherein propylene is produced.
20 . The process of claim 19 , wherein the propylene selectivity is at least about 30%.
21 . The process of claim 20 , wherein the propylene selectivity is at least about 50%.
22 . The process of claim 21 , wherein the propylene selectivity is at least about 60%.
23 . The process of claim 19 , wherein light olefins are produced and the light olefin selectivity is at least about 50%.
24 . The process of claim 23 , wherein the light olefin selectivity is at least about 70%.
25 . The process of claim 24 , wherein the light olefin selectivity is at least about 80%.
26 . The process of claim 20 , wherein light olefins are produced and the light olefin selectivity is at least about 50%.
27 . The process of claim 21 , wherein light olefins are produced and the light olefin selectivity is at least about 70%.
28 . The process of claim 23 , wherein light olefins are produced and the light olefin selectivity is at least about 80%.
29 . The process of claim 1 , wherein the catalyst composition comprises a synthetic porous crystalline material comprising a framework of tetrahedral atoms bridged by oxygen atoms, the tetrahedral atom framework being defined by a unit cell with atomic coordinates in nanometers shown in Table 1, wherein each coordinate position may vary within ±0.05 nanometer.
30 . The process of claim 1 , wherein the synthetic porous crystalline material has an X-ray diffraction pattern including d-spacing and relative intensity values substantially as set forth in Table 2.
31 . The process of claim 29 , wherein the synthetic porous crystalline material has an X-ray diffraction pattern including d-spacing and relative intensity values substantially as set forth in Table 2.
32 . The process of claim 1 , wherein the synthetic porous crystalline material has a composition comprising the molar relationship
X 2 O 3 :(n)YO 2 ,
wherein n is at least about 5, X is a trivalent element, and Y is a tetravalent element.
33 . The process of claim 29 , wherein the synthetic porous crystalline material has a composition comprising the molar relationship
X 2 O 3 :(n)YO 2 ,
wherein n is at least about 5, X is a trivalent element, and Y is a tetravalent element.
34 . The process of claim 30 , wherein the synthetic porous crystalline material has a composition comprising the molar relationship
X 2 O 3 :(n)YO 2 ,
wherein n is at least about 5, X is a trivalent element, and Y is a tetravalent element.
35 . The process of claim 31 , wherein the synthetic porous crystalline material has a composition comprising the molar relationship
X 2 O 3 :(n)YO 2 ,
wherein n is at least about 5, X is a trivalent element, and Y is a tetravalent element.
36 . The process recited in claim 35 , wherein X is a trivalent element selected from the group consisting of boron, iron, indium, gallium, aluminum, and a combination thereof; and Y is a tetravalent element selected from the group consisting of silicon, tin, titanium, germanium, and a combination thereof.
37 . The process recited in claim 36 , wherein X comprises boron or aluminum and Y comprises silicon.
38 . The process of claim 37 , wherein X is aluminum.
39 . The process of claim 1 , wherein the catalyst composition also comprises a large pore molecular sieve having a pore size greater than 6 Angstrom.
40 . The process of claim 39 , wherein the large pore molecular sieve has a pore size greater than 7 Angstrom.
41 . The process of claim 39 , wherein the weight ratio of said synthetic porous crystalline material to the large pore molecular sieve is about 0.005 to about 50.
42 . The process of claim 40 , wherein the weight ratio of said synthetic porous crystalline material to the large pore molecular sieve is about 0.005 to about 50.
43 . The process of claim 41 , wherein the weight ratio of said synthetic porous crystalline material to the large pore molecular sieve is about 0.1 to about 1.0.
44 . The process of claim 42 , wherein the weight ratio of said synthetic porous crystalline material to the large pore molecular sieve is about 0.1 to about 1.0.
45 . The process of claim 11 , wherein the catalyst is metal-stabilized with copper.
46 . The process of claim 1 , wherein the catalyst composition comprises at least one of a zeolite and SAPO.
47 . The process of claim 1 , wherein at least part of the reaction zone is at a temperature of about 500°-600° C.
48 . The process of claim 1 , wherein the process total pressure is about 0.5 to about 10 atmospheres.
49 . The process of claim 48 , wherein the process total pressure is about 1 to about 3 atmospheres.Join the waitlist — get patent alerts
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