US2012222991A1PendingUtilityA1
Novel cracking catalytic compositions
Est. expiryDec 22, 2025(expired)· nominal 20-yr term from priority
Inventors:Paul O'ConnorKing Yen YungAvelino Corma CanosElbert Arjan De GraafErja Paivi Helena Rautiainen
B01J 27/1808C10G 2300/1074C10G 2300/107C10G 2300/1033B01J 27/236C10G 2300/1077B01J 21/16C10G 2300/4093C10G 2400/02B01J 27/1804C10G 11/04B01J 23/007B01J 27/16B82Y 30/00B01J 23/02C10G 51/02
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Claims
Abstract
Novel catalytic compositions for cracking of crude oil fractions are disclosed. The catalytic compositions comprise a basic material. When used in a cracking process, preferably a FCC process, the resulting LCO and HCO fractions have desirably low aromatics levels. Further disclosed is a one-stage FCC process using the catalytic composition of the invention. Also disclosed is a two-stage FCC process for maximizing the LCO yield.
Claims
exact text as granted — not AI-modified1 . An FCC process comprising the step of contacting an FCC feedstock with a catalytic composition under FCC reaction conditions, wherein said catalytic composition comprises a basic material, and wherein said catalytic compositions are substantially free of acidic zeolite.
2 . The process of claim 1 wherein the FCC feedstock is selected from the group consisting of vacuum gas oil, hydrotreated vacuum gas oil, atmospheric resid feed, crude oil, shale oil, tar sand, and mixtures thereof.
3 . The process of claim 1 , which is carried out at a reaction temperature in the range of 400-600° C.
4 . A two-stage cracking process for cracking a feedstock selected from vacuum gasoils, hydrotreated vacuum gasoils, coker gasoils, atmospheric residues, vacuum residues and the hydrotreated products thereof, characterized in that at least one of the stages is a fluid catalytic cracking process in which the catalytic composition comprises a basic material, and wherein said catalytic composition is substantially free of acidic zeolite.
5 . A process according to claim 4 in which the first stage is operated at a reaction temperature of i) 460 to 900° C., ii) between 460 to 600° C., or iii) between 460 to 500° C.
6 . A process according to claim 4 in which both stages are FCC processes, and the second stage is operated at a reaction temperature of i) 480 to 900° C., ii) between 500 to 600° C., or iii) between 530 to 570° C.
7 . A process according to claim 4 in which said FCC process comprises a stripper and a regenerator and the stripper temperature is adjusted between 520 to 600° C. by routing some catalyst from the regenerator to the stripper.
8 . A cracking process according to claim 4 wherein:
a. one of the stages is a hydrocracking process;
b. one of the stages is a hydrocracking process and the first stage is a fluid catalytic cracking process;
c. one of the stages is a hydrocracking process and the first stage is a hydrocracking process; or
d. both of the stages are fluid catalytic cracking processes.
9 . An LCD, HCO, and/or gasoline fraction obtained with the process of claim 8 .
10 . The process according to claim 1 wherein said catalytic composition is substantially free of components having a dehydrogenating activity.
11 . The process according to claim 1 wherein said catalytic composition has sufficient catalytic activity to provide a conversion of FCC feedstock of at least 30% at a CTO ratio of 10 and a reaction temperature below 600° C.
12 . The process according to claim 1 wherein the basic material of said catalytic composition:
a. is selected from the group consisting of compounds of alkali metals, compounds of alkaline earth metals, compounds of trivalent metals, compounds of transition metals, and mixtures thereof;
b. is the oxide, the hydroxide or the phosphate of a transition metal, an alkali metal, an earth alkaline metal, or a transition metal, or a mixture thereof;
c. comprises an alkali metal compound;
d. comprises an alkaline earth metal compound;
e. is a mixed metal oxide;
f. comprises a compound of a transition metal;
g. is a hydrotalcite;
h. is an aluminum phosphate;
i. is doped with a metal cation;
j. is supported on a carrier material;
k. any combination of j) with a)-i);
l. any combination of i) with a)-h); and/or,
m. any combination of a)-j).
13 . The process according to claim 1 wherein the compound of a transition metal of said catalytic composition is selected from the group consisting of ZrO2, Y2O3, Nb2O5, and mixtures thereof; and/or wherein the dopant metal cation is selected from metals of Group IIb, Group IIIb, Group IVb, the rare earth metals, and mixtures thereof; and/or wherein the carrier is a refractory oxide.
14 . A process according to claim 4 in which the catalyst in one of the stages is a traditional acidic zeolite-containing cracking catalyst.
15 . The process according to claim 4 wherein the catalytic composition used in one or more of the fluidized catalytic cracking stages is substantially free of components having a dehydrogenating activity,
16 . The process according to claim 4 wherein the catalytic composition used in one or more of the fluidized catalytic cracking stages is substantially free has sufficient catalytic activity to provide a conversion of FCC feedstock of at least 30% at a CTO ratio of 10 and a reaction temperature below 600° C.
17 . The process according to claim 4 wherein the basic material of said catalytic composition:
a. is selected from the group consisting of compounds of alkali metals, compounds of alkaline earth metals, compounds of trivalent metals, compounds of transition metals, and mixtures thereof;
b. is the oxide, the hydroxide or the phosphate of a transition metal, an alkali metal, an earth alkaline metal, or a transition metal, or a mixture thereof;
c. comprises an alkali metal compound;
d. comprises an alkaline earth metal compound;
e. is a mixed metal oxide;
f. comprises a compound of a transition metal;
g. is a hydrotalcite;
h. is an aluminum phosphate;
i. is doped with a metal cation;
j. is supported on a carrier material;
k. any combination of j) with a)-i);
l. any combination of i) with a)-h); and/or,
m. any combination of a)-j).
18 . The process according to claim 8 wherein the compound of a transition metal of said catalytic composition is selected from the group consisting of ZrO2, Y2O3, Nb2O5, and mixtures thereof; and/or wherein the dopant metal cation is selected from metals of Group IIb, Group IIIb, Group IVb, the rare earth metals, and mixtures thereof; and/or wherein the carrier is a refractory oxide.
19 . The process according to claim 8 wherein the carrier is selected from alumina, silica, silica-alumina, titania, and mixtures thereof; and/or wherein the dopant metal is selected from the group consisting of La, Zn, Zr, and mixtures thereof.
20 . The process according to claim 8 wherein said catalytic composition comprises a material having acidic sites.Cited by (0)
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