Process for alkylation using low ionic liquid volume fraction

Patent metadata

Field	Value
Publication number	US-2016289137-A1
Application number	US-201514675175-A
Country	US
Kind code	A1
Filing date	Mar 31, 2015
Priority date	Mar 31, 2015
Publication date	Oct 6, 2016
Grant date	—

Abstract

An alkylation process utilizing less than 10 vol % of a halometallate based ionic liquid catalyst is described. By decreasing the catalyst volume fraction, the level of subsequent undesirable reactions may be minimized. The total residence time is typically in the range of about 1 min to about 30 min. The alkylate typically has a research octane number of at least about 93, and the olefin conversion is typically at least about 96%.

First claim

What is claimed:

1 . An alkylation process comprising:
passing an isoparaffin having from 4 to 10 carbon atoms to an alkylation reactor; and passing an olefin having from 3 to 10 carbon atoms to the alkyation reactor, wherein the alkylation reactor contains a halometallate based ionic liquid catalyst for reacting the olefin and isoparaffin to generate an alkylate having a research octane number of at least about 93, wherein the alkylation reactor is operated at reaction conditions comprising an operating temperature greater than about 20° C., a molar ratio of isoparaffin to olefin of less than about 20:1, an overall olefin feed rate of greater than about 30 mol olefin/mol ionic liquid catalyst/hr, a total residence time in a range of about 1 min to about 30 min, and less than about 10 vol % of the halometallate based ionic liquid catalyst.

2 . The process of claim 1 wherein the halometallate based ionic liquid catalyst has a viscosity of less than about 120 cSt at a temperature of 25° C., and wherein there is less than about 5 vol % of the halometallate based ionic liquid catalyst.

3 . The process of claim 1 wherein the halometallate based ionic liquid catalyst has a viscosity of less than about 100 cSt at a temperature of 25° C., and wherein there is less than about 4 vol % of the halometallate based ionic liquid catalyst.

4 . The process of claim 1 wherein the halometallate based ionic liquid catalyst has a viscosity of less than about 60 cSt at a temperature of 25° C., and wherein there is less than about 3 vol % of the halometallate based ionic liquid catalyst.

5 . The process of claim 1 wherein there is less than about 5 vol % of the halometallate based ionic liquid catalyst, and wherein the total residence time is the range of about 2 min to about 10 min.

6 . The process of claim 1 wherein there is less than about 4 vol % of the haloaluminate based ionic liquid catalyst, and wherein the total residence time is the range of about 3 min to about 30 min.

7 . The process of claim 1 wherein there is less than about 3 vol % of the haloaluminate based ionic liquid catalyst, and wherein the total residence time is the range of about 4 min to about 30 min.

8 . The process of claim 1 wherein the isoparaffin has 4 carbon atoms and the olefin has 4 carbon atoms and wherein at least one of and the reactions has a selectivity for C 8 of at least about 70%; and the alkylate has a mole ratio of trimethylpentane to dimethylhexane of greater than about 12.

9 . The process of claim 1 wherein the halometallate based ionic liquid is a lactamium based ionic liquid and wherein the total residence time is in the range of about 1 min to about 5 min.

10 . The process of claim 1 wherein an olefin conversion is at least about 96%.

11 . The process of claim 1 further comprising an acid promoter.

12 . The process of claim 11 wherein a molar ratio of olefin to acid promoter of greater than about 15:1.

13 . The process of claim 1 wherein the halometallate based ionic liquid catalyst comprises a phosphonium based ionic liquid, an imidazolium based ionic liquid, a pyridinium based ionic liquid, a pyrrolidinium based ionic liquid, a pyrrolidonium based ionic liquid, or a lactamium based ionic liquid.

14 . The process of claim 1 wherein the halometallate based ionic liquid catalyst comprises tripropylpentylphosphonium heptachloroaluminate, tripropylhexylphosphonium heptachloroaluminate, tributylpentylphosphonium heptachloroaluminate, tributylhexylphosphonium heptachloroaluminate, tributylmethylphosphonium heptachloroaluminate, 1-butyl-3-methyl imidizolium heptachloroaluminate, 1-ethyl-3-methylimidazolium heptachloroaluminate, 1-butylpyridinium heptachloroaluminate, 1-butyl-2-methyl-pyridinium heptachloroaluminate, 1-butyl-3-methyl-pyridinium heptachloroaluminate, 1-butyl-4-methyl-pyridinium heptachloroaluminate, 1-ethyl-1-methylpyrrolidinium heptachloroaluminate, 1-butyl-1-methylpyrrolidinium heptachloroaluminate, caprolactamium heptachloroaluminate, N-methylcaprolactamium heptachloroaluminate, N-methylpyrrolidonium heptachloroaluminate, pyrrolidonium heptachloroaluminate, δ-valerolactamium heptachloroaluminate, N-methyl-δ-valerolactamium heptachloroaluminate or combinations thereof.

15 . An alkylation process comprising:
passing an isoparaffin having 4 carbon atoms to an alkylation reactor; and passing an olefin having 4 carbon atoms to the alkylation reactor, wherein the alkylation reactor contains a haloaluminate based ionic liquid catalyst for reacting the olefin and isoparaffin to generate an alkylate having a research octane number of at least about 93, wherein the alkylation reactor is operated at reaction conditions comprising an operating temperature greater than about 20° C., a molar ratio of isoparaffin to olefin of less than about 20:1, an overall olefin feed rate of greater than about 30 mol olefin/mol ionic liquid catalyst/hr, a total residence time in a range of about 1 min to about 30 min, and less than about 10 vol % of the haloaluminate based ionic liquid catalyst, wherein the haloaluminate based ionic liquid catalyst comprises a phosphonium based ionic liquid, an imidazolium based ionic liquid, a pyridinium based ionic liquid, a lactamium based ionic liquid, and wherein an olefin conversion is at least about 96%.

16 . The process of claim 15 wherein the haloaluminate based ionic liquid has a viscosity of less than about 120 cSt at a temperature of 25° C., and wherein there is less than about 5 vol % of the ionic liquid catalyst.

17 . The process of claim 15 wherein there is less than about 5 vol % of the halometallate based ionic liquid catalyst, and wherein the total residence time is the range of about 2 min to about 10 min.

18 . The process of claim 15 wherein there is less than about 4 vol % of the haloaluminate based ionic liquid, and wherein the total residence time is the range of about 3 min to about 30 min.

19 . The process of claim 15 wherein at least of: the research octane number is at least about 95; the reaction has a selectivity for C 8 of at least about 70%; and the alkylate has a mole ratio of trimethylpentane to dimethylhexane of greater than about 12.

20 . The process of claim 15 wherein the ionic liquid catalyst comprises tripropylpentylphosphonium heptachloroaluminate, tripropylhexylphosphonium heptachloroaluminate, tributylpentylphosphonium heptachloroaluminate, tributylhexylphosphonium heptachloroaluminate, tributylmethylphosphonium heptachloroaluminate, 1-butyl-3-methyl imidizolium heptachloroaluminate, 1-ethyl-3-methylimidazolium heptachloroaluminate, 1-butylpyridinium heptachloroaluminate, 1-butyl-2-methyl-pyridinium heptachloroaluminate, 1-butyl-3-methyl-pyridinium heptachloroaluminate, 1-butyl-4-methyl-pyridinium heptachloroaluminate, 1-ethyl-1-methylpyrrolidinium heptachloroaluminate, 1-butyl-1-methylpyrrolidinium heptachloroaluminate, caprolactamium heptachloroaluminate, N-methylcaprolactamium heptachloroaluminate, N-methylpyrrolidonium heptachloroaluminate, pyrrolidonium heptachloroaluminate, δ-valerolactamium heptachloroaluminate, N-methyl-δ-valerolactamium heptachloroaluminates, or combinations thereof.

Assignees

• Uop Llc

Inventors

• Buchbinder Avram M
• Martins Susie C
• Broderick Erin M
• Barger Paul T
• Bhattacharyya Alakananda C
• Nafis Douglas A

Classifications

• C10L1/06

  for spark ignition · CPC title

• C10G2300/305

  Octane number, e.g. motor octane number [MON], research octane number [RON] · CPC title

• C10G29/205

  by reaction with hydrocarbons added to the hydrocarbon oil · CPC title

• C07C2531/02

  containing organic compounds or metal hydrides · CPC title

• C07C2527/126

  Aluminium chloride · CPC title