Process to produce paraffinic hydrocarbon fluids from light paraffins

Patent metadata

Field	Value
Publication number	US-10023533-B2
Application number	US-201615387996-A
Country	US
Kind code	B2
Filing date	Dec 22, 2016
Priority date	Dec 16, 2014
Publication date	Jul 17, 2018
Grant date	Jul 17, 2018

Abstract

A process for converting light paraffins to heavier paraffinic hydrocarbon fluids is disclosed. The process involves: (1) oxidation of iso-paraffins to alkyl hydroperoxides and alcohols; (2) conversion of the alkyl hydroperoxides and alcohols to dialkyl peroxides; and (3) radical-initiated coupling of paraffins and/or iso-paraffins using the dialkyl peroxides as radical initiators, thereby forming heavier hydrocarbon products. Fractionation of the heavy hydrocarbon products can then be used to isolate fractions for use as hydrocarbon fluids.

First claim

The invention claimed is:

1. A process for the conversion of paraffins to paraffinic hydrocarbon fluids, comprising:
a) oxidizing iso-paraffins from a first paraffinic feed with air or oxygen to form alkylhydroperoxides and alcohols;
b) catalytically reacting the alkyl hydroperoxides with said alcohols from step (a) to form dialkyl peroxides; and
c) providing a second paraffinic feed comprising paraffins using the dialkyl peroxides from step (b) as radical initiators to couple paraffins with paraffins to create paraffinic hydrocarbon fluids comprising other branched and heavier paraffins and a second alcohol;
wherein the first paraffinic feed and the second paraffinic feed are independently selected from normal paraffins with 4 or 5 carbon numbers, iso-paraffins with 4 or 5 carbon numbers, and mixtures thereof.

2. The process of claim 1 , further comprising isomerizing at least a fraction of the normal paraffins to iso-paraffins prior to step (a).

3. The process of claim 1 , further comprising fractionating the paraffinic hydrocarbon fluids to isolate a desired fraction.

4. The process of claim 1 , wherein the iso-paraffins of step (a) are selected from iso-butane, iso-pentane, and mixtures thereof.

5. The process of claim 1 , wherein the iso-paraffins of step (a) comprise 60 to 99 wt % iso-butane.

6. The process of claim 1 , wherein the second paraffinic feed comprises less than 50 wt % olefins.

7. The process of claim 1 , wherein the second paraffinic feed comprises less than 10 wt % olefins.

8. The process of claim 1 , wherein the second paraffinic feed comprises less than 5 wt % olefins.

9. The process of claim 1 , wherein the first paraffinic feed comprises butanes.

10. The process of claim 9 , wherein the first paraffinic feed comprises 5 to 90 wt % iso-butane.

11. The process of claim 9 , further comprising substantially isomerizing n-butane in the first paraffinic feed to iso-butane.

12. The process of claim 1 , wherein the first paraffinic feed comprises pentanes.

13. The process of claim 12 , wherein the first paraffinic feed comprises 5 to 90 wt % iso-pentane.

14. The process of claim 12 further comprising substantially isomerizing n-pentane in the first paraffinic feed to iso-pentane.

15. The process of claim 1 , wherein iso-paraffins are separated from normal paraffins in the first paraffinic feed, and the separated normal paraffins are used as the second paraffinic feed.

16. The process of claim 1 , wherein iso-paraffins are separated from normal paraffins in the first paraffinic feed, and the separated iso-paraffins are used as the second paraffinic feed.

17. The process of claim 1 , wherein the paraffinic hydrocarbon fluids are hydro-finished to remove trace oxygenates or unsaturation.

18. The process of claim 1 , the reaction in step (b) is carried out by reactive distillation.

19. The process of claim 1 , wherein the coupling reaction of step (c) is carried out in a reactor selected from batch, CSTR, and plug-flow.

20. A process for the conversion of iso-butane and normal butane to paraffinic hydrocarbon fluids, comprising:
a) oxidizing iso-butane to form t-butyl hydroperoxide and t-butyl alcohol;
b) catalytically reacting the t-butyl hydroperoxide with the t-butyl alcohol from step (a) to di-t-butyl peroxide; and
c) providing a paraffinic feed comprising paraffins using the di-t-butyl peroxide from step (b) as a radical initiator to couple paraffins with paraffins to create hydrocarbon fluids comprising other branched and heavier paraffins and a second alcohol, wherein the paraffinic feed comprises normal butane, iso-butane, or mixtures thereof.

21. The process of claim 20 , further comprising: (d) fractionating the hydrocarbon fluids to isolate C8 and C12 fractions.

22. The method of claim 20 , wherein the paraffinic feed comprises less than 10 wt % olefins.

23. The method of claim 20 , wherein the paraffinic feed comprises less than 5 wt % olefins.

24. The method of claim 20 , wherein the hydrocarbon fluids are hydro-finished to remove trace oxygenates or unsaturation.

Assignees

• Exxonmobil Res & Eng Co

Inventors

• Wang Kun

Classifications

• C07C2/862

  the non-hydrocarbon contains only oxygen as hetero-atoms · CPC title

• C10G69/126

  polymerisation, e.g. oligomerisation · CPC title

• C10G2300/1025

  Natural gas · CPC title

• C07C29/132

  by reduction of an oxygen containing functional group · CPC title

• C10G2300/1081

  Alkanes · CPC title