Simultaneous dehydration and skeletal isomerisation of isobutanol on acid catalysts

Patent metadata

Field	Value
Publication number	US-9233886-B2
Application number	US-201113582759-A
Country	US
Kind code	B2
Filing date	Mar 15, 2011
Priority date	Mar 15, 2010
Publication date	Jan 12, 2016
Grant date	Jan 12, 2016

Abstract

The present invention (in a first embodiment) relates to a process for the simultaneous dehydration and skeletal isomerization of isobutanol to make substantially corresponding olefins, having the same number of carbons and consisting essentially of a mixture of n-butenes and iso-butene, said process comprising:
a) introducing in a reactor a stream (A) comprising isobutanol, optionally water, optionally an inert component, b) contacting said stream with a catalyst in said reactor at conditions effective to dehydrate and skeletal isomerize at least a portion of the isobutanol to make a mixture of n-butenes and iso-butene, c) recovering from said reactor a stream (B), removing water, the inert component if any and unconverted isobutanol if any to get a mixture of n-butenes and iso-butene,

Wherein,
the WHSV of the isobutanol is at least 1 h −1 or the temperature is from 200° C. to 600° C. and the catalyst is capable to make simultaneously the dehydration and skeletal isomerization of butene.

The catalyst is a crystalline silicate of the group FER, MWW, EUO, MFS, ZSM-48, MTT, MFI, MEL or TON having Si/Al higher than 10,
or a dealuminated crystalline silicate of the group FER, MWW, EUO, MFS, ZSM-48, MTT, MFI, MEL or TON having Si/Al higher than 10, or a phosphorus modified crystalline silicate of the group FER, MWW, EUO, MFS, ZSM-48, MTT, MFI, MEL or TON having Si/Al higher than 10, or a silicoaluminaphosphate molecular sieve of the group AEL, or a silicated, zirconated or titanated or fluorinated alumina.

Advantageously the stream (B) is fractionated in a step d) to produce a n-butenes stream (N) and to remove the essential part of isobutene optionally recycled with stream (A) to the dehydration/isomerization reactor of step b).

First claim

What is claimed:

1. A process for the simultaneous dehydration and skeletal isomerisation of isobutanol to make substantially corresponding olefins, having the same number of carbons and including a mixture of n-butenes and iso-butene, said process comprising:
a) introducing in a reactor a stream (A) comprising isobutanol, optionally water, and optionally an inert component, wherein the isobutanol is present in the stream (A) in an amount ranging from 30 to 100 weight percent based on a total weight of the stream (A),
b) contacting said stream (A) with a catalyst in said reactor at conditions effective to dehydrate and skeletal isomerase the iso-butyl moiety of at least a portion of the isobutanol to make a mixture of n-butenes and iso-butene,
c) recovering from said reactor a stream (B), removing water, the inert component if any and unconverted isobutanol if any to get a mixture of n-butenes and iso-butene,
wherein the WHSV of the isobutanol is at least 1 h −1 and the catalyst is capable of simultaneously catalyzing the dehydration of the isobutanol and skeletal isomerization of butene; and
wherein the catalyst is:
a crystalline silicate of the group FER, MWW, EUO, MFS, ZSM-48, MTT, MFI, MEL or TON having Si/Al higher than 10,
or a dealuminated crystalline silicate of the group FER, MWW, EUO, MFS, ZSM-48, MTT, MFI, MEL or TON having Si/Al higher than 10,
or a phosphorus modified crystalline silicate of the group FER, MWW, EUO, MFS, ZSM-48, MTT, MFI, MEL or TON having Si/Al higher than 10,
or a silicoaluminaphosphate molecular sieve of the group AEL,
or a silicated, zirconated or titanated or fluorinated alumina.

2. The process according to claim 1 wherein the WHSV of the isobutanol is from 1 to 30 h −1 .

3. The process according to claim 2 wherein the WHSV of the isobutanol is from 2 to 21 h −1 .

4. A process for the simultaneous dehydration and skeletal isomerisation of isobutanol to make substantially corresponding olefins, having the same number of carbons and including a mixture of n-butenes and iso-butene, said process comprising:
a) introducing in a reactor a stream (A) comprising isobutanol, optionally water, and optionally an inert component, wherein the isobutanol is present in the stream (A) in an amount ranging from 30 to 100 weight percent based on a total weight of the stream (A),
b) contacting said stream (A) with a catalyst in said reactor at conditions effective to dehydrate and skeletal isomerise the iso-butyl moiety of at least a portion of the isobutanol to make a mixture of n-butenes and iso-butene,
c) recovering from said reactor a stream (B), removing water, the inert component if any and unconverted isobutanol if any to get a mixture of n-butenes and iso-butene,
wherein the temperature in the reactor ranges from 200° C. to 600° C. and the catalyst is capable of simultaneously catalyzing the dehydration the isobutanol and skeletal isomerization of butene; and
wherein the catalyst is:
a crystalline silicate of the group FER, MWW, EUO, MFS, ZSM-48, MTT, MFI, MEL or TON having Si/Al higher than 10,
or a dealuminated crystalline silicate of the group FER, MWW, EUO, MFS, ZSM-48, MTT, MFI, MEL or TON having Si/Al higher than 10,
or a phosphorus modified crystalline silicate of the group FER, MWW, EUO, MFS, ZSM-48, MTT, MFI, MEL or TON having Si/Al higher than 10,
or a silicoaluminaphosphate molecular sieve of the group AEL,
or a silicated, zirconated or titanated or fluorinated alumina.

5. The process according to claim 4 wherein the pressure of the reactor ranges from 0.5 to 10 bars absolute.

6. The process according to claim 4 wherein the temperature ranges from 250° C. to 500° C.

7. The process according to claim 6 wherein the temperature ranges from 300° C. to 450° C.

8. The process according to claim 4 wherein the stream (B) is fractionated in a step d) to produce an n-butenes stream (N) and to remove isobutene optionally recycled with stream (A) to the reactor of step b).

9. The process according to claim 8 wherein in the fractionation of step d) iso-butene is removed by selective oligomerisation of iso-butene.

10. The process according to claim 8 wherein in the fractionation of step d) iso-butene is removed by selective etherification with methanol or ethanol.

11. The process according to claim 8 wherein in the fractionation of step d) iso-butene is removed by selective hydration into t-butanol.

12. The process according to claim 11 wherein said t-butanol is recycled to the reactor at step b).

13. The process according to claim 8 wherein the fractionation of step d) is made by a catalytic distillation column wherein 1-butene is isomerised to 2-butene, iso-butene is recovered as overhead and 2-butene is recovered in a bottoms of said catalytic distillation column.

14. The process according to claim 13 wherein iso-butene is recycled to the reactor at step b).

15. The process according to claim 14 wherein among the butenes produced at step c) the proportion of n-butenes is above 20%.

16. The process according to claim 15 wherein among the butenes produced at step c) the proportion of n-butenes is above 30%.

17. The process according to claim 16 wherein among the butenes produced at step c) the proportion of n-butenes is above 40%.

18. The process according to claim 17 wherein among the butenes produced at step c) the proportion of n-butenes is above 50%.

19. The process according to claim 1 , wherein the catalyst is the silicoaluminaphosphate molecular sieve of the group AEL.

20. The process according to claim 1 , wherein the catalyst is the silicated, zirconated or titanated or fluorinated alumina.

21. The process according to claim 1 , wherein the catalyst is the crystalline silicate of the group FER, MWW, EUO, MFS, ZSM-48, MTT, MFI, MEL or TON having Si/Al higher than 10.

22. The process according to claim 1 , wherein the catalyst is the dealuminated crystalline silicate of the group FER, MWW, EUO, MFS, ZSM-48, MTT, MFI, MEL or TON having Si/Al higher than 10.

23. The process according to claim 1 , wherein the catalyst is the phosphorus modified crystalline silicate of the group FER, MWW, EUO, MFS, ZSM-48, MTT, MFI, MEL or TON having Si/Al higher than 10.

24. The process according to claim 1 , wherein the catalyst is a crystalline silicate of the group FER or MFI having Si/Al higher than 10, a dealuminated crystalline silicate of the group FER or MFI having Si/Al higher than 10, or a phosphorus modified crystalline silicate of the group FER or MFI having Si/Al higher than 10.

25. The process according to claim 1 , wherein the mixture of n-butenes and iso-butene contains from 35 to 50 weight percent iso-butene.

26. The process according to claim 1 , a ratio of isobutanol to all other C 4 alcohols in the stream (A) is 42% or above.

27. The process according to claim 1 , a ratio of isobutanol to all other C 4 alcohols in the stream (A) is 70% or above.

28. The process according to claim 1 , a ratio of isobutanol to all other C 4 alcohols in the stream (A) is 80% or above.

Assignees

• Adam Cindy
• Minoux Delphine
• Nesterenko Nikolai
• Van Donk Sander
• Dath Jean-Pierre
• Total Res & Technology Feluy

Inventors

• Adam Cindy
• Minoux Delphine
• Nesterenko Nikolai
• Van Donk Sander
• Dath Jean-Pierre

Classifications

• C07C2529/40

  of the pentasil type, e.g. types ZSM-5, ZSM-8 or ZSM-11 · CPC title

• C07C11/08

  with four carbon atoms · CPC title

• C07C11/09

  Isobutene · CPC title

• B01J29/85

  Silicoaluminophosphates [SAPO compounds] · CPC title

• C07C2529/70

  of types characterised by their specific structure not provided for in groups C07C2529/08 - C07C2529/65 · CPC title