Isomerization and catalytic activation of pentane-enriched hydrocarbon mixtures

Patent metadata

Field	Value
Publication number	US-10981847-B2
Application number	US-201916593238-A
Country	US
Kind code	B2
Filing date	Oct 4, 2019
Priority date	Oct 8, 2018
Publication date	Apr 20, 2021
Grant date	Apr 20, 2021

Abstract

The present disclosure relates to processes that catalytically convert a hydrocarbon feed stream predominantly comprising both isopentane and n-pentane to yield upgraded hydrocarbon products that are suitable for use either as a blend component of liquid transportation fuels or as an intermediate in the production of other value-added chemicals. The hydrocarbon feed stream is isomerized in a first reaction zone to convert at least a portion of the n-pentane to isopentane, followed by catalytic-activation of the isomerization effluent in a second reaction zone with an activation catalyst to produce an activation effluent. The process increases the conversion of the hydrocarbon feed stream to olefins and aromatics, while minimizing the production of C1-C4 light paraffins. Certain embodiments provide for further upgrading of at least a portion of the activation effluent by either oligomerization or alkylation.

First claim

We claim:

1. A method for converting a feed stream comprising pentanes to produce liquid hydrocarbons comprising monocyclic aromatics, comprising:
a. providing a hydrocarbon feed stream comprising at least 50 wt. % pentanes, including both n-pentane and isopentane;
b. contacting the hydrocarbon feed stream with one or more isomerization catalysts in a first reaction zone that is maintained at a temperature and a pressure that facilitates isomerization of at least a portion of the n-pentane in the hydrocarbon feed stream to isopentane, thereby producing an isomerization effluent characterized by an increased ratio of isopentane to n-pentane relative to the hydrocarbon feed stream;
c. contacting the isomerization effluent with an activation catalyst in a second reaction zone that is maintained at a temperature and pressure that facilitates at least one reaction selected from dehydrogenation, cracking and aromatization, thereby converting at least a portion of hydrocarbons present in the isomerization effluent to produce an activation effluent comprising olefins containing from two to five carbon atoms, monocyclic aromatics and unconverted alkanes containing from two to five carbon atoms; and
d. at least partially condensing the activation effluent to produce a liquid hydrocarbons fraction and a gaseous light hydrocarbons fraction, wherein the liquid hydrocarbons fraction comprises monocyclic aromatics and unreacted alkanes containing at least five carbon atoms, wherein the gaseous light hydrocarbons fraction comprises at least 80 wt. % hydrocarbons containing four or fewer carbon atoms and hydrogen.

2. The method of claim 1 , further comprising separating the liquid hydrocarbons fraction into an aromatics fraction and an unreacted C5/C6 hydrocarbons fraction, wherein the aromatics fraction comprises monocyclic aromatics suitable for use as a blend component of gasoline and the unreacted C5/C6 hydrocarbons fraction comprises alkanes and olefins containing from five to six carbons that is optionally mixed with the hydrocarbon feed stream of part a).

3. The method of claim 1 , wherein the hydrocarbon feed stream comprises at least 5 wt. % of hydrocarbons containing four or fewer carbon atoms.

4. The method of claim 1 , wherein the hydrocarbon feed stream comprises at least 60 wt. % pentanes.

5. The method of claim 1 , wherein the activation catalyst comprises one or more zeolites characterized by Si/Al ratio ranging from 12 to 80.

6. The method of claim 1 , wherein the activation catalyst comprises ZSM-5 zeolite.

7. The method of claim 1 , wherein the activation catalyst facilitates at least one reaction selected from the group consisting of oligomerization, dehydrogenation, and aromatization.

8. The method of claim 1 , wherein the first reaction zone is maintained at a temperature in a range from 500° C. to 625° C. and a pressure in the range from 15 psig to 100 psig.

9. The method of claim 8 , wherein the diluent is added in an amount that alters the specificity of the activation catalyst to increase the production of olefins, decrease the production of aromatics, or combinations thereof, thereby increasing a ratio of olefins to aromatics in the activation effluent.

10. The method of claim 8 , wherein the diluent is added in an amount that is effective to produce an activation effluent characterized by an olefins to aromatics ratio in a range of 0.5 to 2.0.

11. The method of claim 8 , wherein the diluent is added in an amount that is effective to produce an activation effluent characterized by an olefins to aromatics ratio in a range of 0.5 to 1.0.

12. The method of claim 8 , wherein the diluent is selected from methane, ethane, propane, butanes, and combinations thereof.

13. The method of claim 1 , wherein the temperature in the first reaction zone is maintained at a temperature in a range from 525° C. to 600° C. and a pressure in the range from 15 psig to 75 psig.

14. The method of claim 1 , wherein the second reaction zone is maintained at a temperature in a range from 550° C. to 600° C. and a pressure in the range from 20 psig to 60 psig.

15. The method of claim 1 , wherein the second reaction zone is maintained at a temperature in a range from 575° C. to 600° C. and a pressure in the range from 20 psig to 50 psig.

16. The method of claim 1 , further comprising adding a diluent to at least one of the hydrocarbon feed stream and the isomerization effluent prior to the contacting with the activation catalyst, wherein the diluent is characterized as less likely to react with the activation catalyst than the hydrocarbon feed stream at the conditions of temperature and pressure that are maintained in the first reaction zone, and wherein the diluent is characterized as less likely to react with the activation catalyst than molecules present in the isomerization effluent at the conditions of temperature and pressure that are maintained in the second reaction zone.

17. The method of claim 1 , further comprising adding a diluent to at least one of the hydrocarbon feed stream and the isomerization effluent prior to the contacting with the activation catalyst, wherein the diluent does not react with the isomerization catalyst at the conditions of temperature and pressure that are maintained in the first reaction zone, and wherein the diluent does not react with the activation catalyst at the conditions of temperature and pressure that are maintained in the second reaction zone.

18. The method of claim 1 , wherein the hydrocarbon feed stream is contacted with one or more isomerization catalysts contained within in multiple reaction zones that are arranged in a series configuration.

Assignees

• Phillips 66 Co

Inventors

• Baldridge Anthony O
• Mcdaniel Neal D
• Suttil James A
• Weintrob Edward C
• Yao Jianhua
• Randolph Bruce B
• Sardashti Maziar
• Walston Robert M
• Lusk Steven E

Classifications

• C10L2270/023

  for gasoline engines · CPC title

• C10G2300/1081

  Alkanes · CPC title

• C07C5/333

  Catalytic processes · CPC title

• C10L1/06

  for spark ignition · CPC title

• C10G63/04

  including at least one cracking step · CPC title