US2006070918A1PendingUtilityA1
Method to extend the utilization of a catalyst in a multistage reactor system
Est. expiryOct 1, 2024(expired)· nominal 20-yr term from priority
B01J 8/0457C10G 65/02B01J 8/0085B01J 2208/00707B01J 2219/0004B01J 8/00B01J 8/04C10G 65/04B01J 35/19
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Claims
Abstract
The invention provides a method to extend the utilization of a catalyst in a multistage reaction system, provided that a primary reaction and a secondary (or more) catalyst-poisoning reaction occur on the same catalyst, and the rate of the secondary (or more), catalyst-poisoning reaction is faster than the rate of the primary reaction.
Claims
exact text as granted — not AI-modified1 . A method for extending catalyst utilization comprising:
(a) passing a feedstock and hydrogen through at least two serially-connected reactors in positions R 1 , R 2 , . . . . R n , wherein n is the number of reactors, each reactor containing a catalyst, for a period until the catalyst in at least one most upstream reactor is deactivated for a secondary catalytic reaction or until the product from the most downstream reactor fails to meet a desired specification; (b) bypassing the at least one most upstream reactor containing the deactivated catalyst of step (a) to pass the feedstock and hydrogen into at least one downstream reactor; (c) reloading the at least one bypassed reactor of step (b) with fresh catalyst; (d) placing the at least one reloaded reactor of step (c) downstream of at least one of the serially-connected reactors that were not reloaded with fresh catalyst in step (c); and (e) repeating steps (a) through (d) to meet the product specification.
2 . The method of claim 1 , wherein the catalyst is selected from the group consisting of a zero-valent element of one or more of the Group VIII elements of the Periodic Table.
3 . The method of claim 2 , wherein the catalyst is selected from the group consisting of Fe, Co, Ni, Ru, Rh, Pd, Os, Ir, and Pt.
4 . The method of claim 2 , wherein the catalyst is a porous metal structure.
5 . The method of claim 4 , wherein the catalyst comprises Raney® nickel.
6 . The method of claim 2 , wherein the catalyst is supported on a support.
7 . The method of claim 6 , wherein the support is selected from the group consisting of carbon, alumina, silica, titania, silica-alumina, silica-titania, titania-alumina, clays, aluminosilicates, zeolites, water insoluble salts of calcium, water insoluble salts of barium, water insoluble salts of strontium, compounds thereof and combinations thereof.
8 . The method of claim 7 , wherein the catalyst comprises nickel with heavy nickel loading supported on extrudates of silica/alumina.
9 . The method of claim 1 , wherein the pressure is from about 100 kPa to about 20 MPa.
10 . The method of claim 1 , wherein the hydrogen is fed to one or more of the reactors.
11 . The method of claim 1 , wherein the temperature is from about minus 50° C. to about 400° C.
12 . The method of claim 1 , further comprising adjusting the temperature to compensate for the number of serially-connected reactors in each of steps (b) and (d) for obtaining product with the desired specifications.
13 . The method of claim 1 , wherein the feedstock is an organic liquid comprising a compound that can be hydrogenated by a catalyst of one or more of the Group VIII elements of the Periodic Table.
14 . The method of claim 1 , wherein in step (d) the at least one reloaded reactor is placed downstream of the most downstream reactor that was not reloaded with the fresh catalyst in step (c).
15 . A method for extending catalyst utilization comprising:
(a) passing an organic feedstock and hydrogen through at least two serially-connected reactors in positions, R 1 , R 2 , . . . R n , wherein n is the number of reactors, each reactor containing a porous metal or supported catalyst, for a period until the catalyst in at least one most upstream reactor is deactivated for desulfurization or until the product from the most downstream reactor fails to meet a desired specification; (b) bypassing the at least one most upstream deactivated reactor of step (a) to pass the feedstock and the hydrogen into downstream reactors; (c) reloading the at least one bypassed reactor of step (b) with fresh catalyst; (d) placing the at least one reloaded reactor of step (c) downstream; and (e) repeating steps (a) through (d) to meet a desired specification.
16 . The method of claim 15 , wherein the temperature is from about minus 50° C. to about 400° C.
17 . The method of claim 15 , wherein the pressure is from about 100 kPa to about 20 MPa.
18 . The method of claim 15 , further comprising adjusting the temperature to compensate for the number of serially-connected reactors in each of steps (b) and (d) to meet the desired product specifications.
19 . The method of claim 15 , wherein the feedstock comprises 1,3-propanediol.
20 . The method of claim 15 , wherein in step (d) the at least one reloaded reactor is placed last in the reactor series, in position Rn.
21 . The method of claim 15 , wherein the catalyst comprises nickel with heavy nickel loading supported on extrudates of silica/alumina.
22 . A method for extending catalyst utilization comprising:
(a) passing a biochemically-derived organic feedstock containing 1,3-propanediol and hydrogen through at least two serially-connected reactors in positions R 1 , R 2 , . . . R n , wherein n is the number of reactors, each reactor containing a catalyst comprising nickel with heavy nickel loading supported on extrudates of silica/alumina, for a period until the catalyst in the most upstream reactor is deactivated for desulfurization or until the product from the most downstream reactor fails to meet a desired specification; (b) bypassing the reactor in position R 1 to pass the feedstock and the hydrogen into the reactor in position R 2 ; (c) reloading the bypassed reactor of step (b) with fresh catalyst; (d) placing the reloaded reactor of step (c) in the reactor series downstream at position Rn; and (e) repeating steps (a) through (d) to meet a desired specification.
23 . The method of claim 22 further comprising adjusting the temperature to compensate for the number of serially-connected reactors in each of steps (b) and (d).
24 . The method of claim 22 , wherein the temperature is from about minus 50° C. to about 200° C.
25 . The method of claim 22 , wherein the temperature is from about 80° C. to about 140° C.Join the waitlist — get patent alerts
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