US2006138023A1PendingUtilityA1
Process for making a lube basestock
Est. expiryOct 2, 2020(expired)· nominal 20-yr term from priority
Inventors:William J. MurphyGary B. McvickerSylvain HantzerIan A. CodyStuart L. SoledSandra J. LinekJoseph E. Baumgartner
B01J 29/7484B01J 23/40B01J 29/068B01J 29/44B01J 29/80C10G 45/64C10G 2400/10B01J 35/394B01J 35/19
41
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Claims
Abstract
A method for hydroisomerizing a waxy feed to favor one of VI or yield is described. The method uses a unitized pellet powder catalyst comprising a metal hydrogeneration component, a first catalytic component selected from 8, 10 and 12 ring moleular sieves and mixtures thereof, and a second amorphous isomerization component which is an amorphous inorganic oxide. Importantly, the ratio of feed and second components are present in a predetermined ratio to provide a preselected acidity favoring one of VI or yield resulting from the hydroisomerization.
Claims
exact text as granted — not AI-modified1 . A method for hydroisomerizing a waxy feed to produce improved yield of a lube basestock which comprises:
(a) contacting the waxy feed under hydroisomerization conditions with a catalyst comprising a unitized mixed powdered pellet catalyst, said catalyst comprising:
(i) a first dewaxing component selected from 8, 10 and 12 ring molecular sieves and mixtures thereof having a metal hydrogenation component dispersed thereon;
(ii) a second isomerization component which is an amorphous inorganic oxide said second component having a metal hydrogenation component dispersed thereon; and
(iii) wherein the first and second components are present in a ratio such that when evaluated in the conversion of methyl cyclohexane at 320° C. to 1,1-dimethylcyclopentane, 1,2-dimethylcyclopentane, 1,3-dimethylcyclopentane and ethylcyclopentane, the catalyst will provide a trans-1,2-/trans-1,3-dimethylcyclopentane ratio in the range of less than about 1 and a selectivity to ethylcyclopentane, at 10% conversion, of at least about 50%.
2 . The method of claim 1 wherein the dewaxing component is at least one of a 10 ring and 12 ring molecular sieve.
3 . The method of claim 1 wherein the isomerization component is at least one of silica, alumina, titania, zirconia, silica-alumina and silica-magnesia.
4 . The method of claim 3 wherein the isomerization component is at least one of silica, alumina, titania, and zirconia.
5 . The method of claim 1 wherein the hydrogenation component is a Group VIII metal.
6 . The method of claim 5 wherein the hydrogenation component is selected from Pt, Pd, and mixtures thereof.
7 . The method of claim 6 wherein the hydrogenation component is dispersed in an amount ranging from about 0.1 wt. % to about 30 wt. %.
8 . The method of claim 1 wherein the amorphous inorganic oxide is promoted or doped with yttria, rare earth oxides, boria and magnesia.
9 . The method of claim 1 wherein the feed is a feed that is solvent dewaxed to a pour point of up to +10° C.
10 . A method for hydroisomerizing a waxy feed to produce improved yield of a lube basestock which comprises:
(a) contacting the waxy feed under hydroisomerization conditions with a catalyst comprising a unitized mixed powdered pellet catalyst, said catalyst comprising:
(i) a first dewaxing component selected from 8, 10 and 12 ring molecular sieves and mixtures thereof having a metal hydrogenation component dispersed thereon;
(ii) a second isomerization component which is an amorphous inorganic oxide said second component having a metal hydrogenation component dispersed thereon; and
(iii) wherein said first and second components are present in a ratio such that when evaluated in the conversion of methyl cyclohexane at 320° C. to 1,1-dimethylcyclopentane, 1,2-dimethylcyclopentane, 1,3-dimethylcyclopentane and ethylcyclopentane, the catalyst will provide a trans-1,2-/trans-1,3-dimethylcyclopentane ratio in the range of at least 1 and a selectivity to ethylcyclopentane, at 10% conversion, of at least about 50%.
11 . A method for hydroisomerizing a waxy feed to produce improved yield of a lube basestock which comprises:
(a) contacting the waxy feed under hydroisomerization conditions with a catalyst comprising a unitized mixed powdered pellet catalyst, said catalyst comprising:
(i) at least one first component selected from 8, 10 and 12 ring molecular sieves, and mixtures thereof, having a metal hydrogenation component dispersed thereon;
(ii) at least one second component selected from 8, 10 and 12 ring molecular sieves, and mixtures thereof, having a metal hydrogenation component dispersed thereon; and
(iii) wherein said first and second components are present in a ratio such that when evaluated in the conversion of methyl cyclohexane at 320° C. to 1,1-dimethylcyclopentane, 1,2-dimethylcyclopentane, 1,3-dimethylcyclopentane and ethylcyclopentane, the catalyst will provide a trans-1,2-/trans-1,3-dimethylcyclopentane ratio in the range of less than about 1 and a selectivity to ethylcyclopentane, at 10% conversion, of at least about 50%.
12 . The method of claim 11 wherein the dewaxing component is at least one of a 10 ring and 12 ring molecular sieve.
13 . The method of claim 11 wherein the 10 and 12 ring molecular sieves are selected from alumino silicates and alumino phosphates.
14 . The method of claim 13 wherein the alumino silicates are selected from ZSM -5, ZSM-11, ZSM-12, ZSM-22, ZSM-23, ZSM-35, natural and synthetic ferrierites, ZSM-48, ZSM-57, SSZ-31, Beta, Mordenite, Offretite, ECR-42, MCM-71, and ITQ-13.
15 . The method of claim 14 wherein said at least one first component is ITQ-13 and said at least one second component is selected from ZSM-48, ZSM-35, ZSM-22, ZSM-23, ZSM-57, SSZ-31, and mixtures thereof.
16 . The method according to claim 14 wherein said at least one first component is selected from ITQ-13, ZSM-57, and mixtures thereof, and said at least one second component is selected from ZSM-22, ZSM-23, ZSM-35, ZSM-48, SSZ-31, and mixtures thereof.
17 . The method according to claim 11 wherein said first and second components are present in a ratio such that when evaluated in the conversion of methyl cyclohexane at 320° C. to 1,1-dimethylcyclopentane, 1,2-dimethylcyclopentane, 1,3-dimethylcyclopentane and ethylcyclopentane, the catalyst will provide a trans-1,2-/trans-1,3-dimethylcyclopentane ratio in the range of less at least 1 and a selectivity to ethylcyclopentane, at 10% conversion, of at least about 50%.Cited by (0)
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