2,3,3,3-tetrafluoro-1-propene as diluent for the preparation of novel butyl rubbers

Patent metadata

Field	Value
Publication number	US-10011670-B2
Application number	US-201515307125-A
Country	US
Kind code	B2
Filing date	Apr 30, 2015
Priority date	Apr 30, 2014
Publication date	Jul 3, 2018
Grant date	Jul 3, 2018

Abstract

The invention relates to an efficient polymerization process and its use to produce novel copolymers with a specific micro structure. In particular, the invention relates to butyl rubbers with novel micro structure, preferably those obtainable by copolymerization of monomer mixtures comprising isobutylene and isoprene in diluents comprising 2,3,3,3 -tetrafluoro-1-propene. In a further aspect the invention relates to halogenated copolymers obtainable from such novel copolymers by halogenation.

First claim

The invention claimed is:

1. Halogenated copolymers at isobutylene and isoprene having a copolymer sequence distribution defined by equation (I)
F=mA /(1 −mA ) 2   (eq. I)

wherein
A is the molar ratio of isoprene to isobutylene in the halogenated copolymer as determined by 1 H NMR;
F is the isobutylene-isoprene-isoprene triad traction in the copolymer as determined by 13 C NMR; and
m is in the range of
[1.35−(0.03× MOC )]≥ m≥[ 1.15−(0.03× MOC )]

whereby MOC is the content of isoprene in the halogenated copolymer in mol-% as determined by 1 H NMR.

2. The halogenated copolymers according to claim 1 , wherein
[1.35−(0.028× MOC )]≥ m≥[ 1.16−(0.028× MOC )].

3. The halogenated copolymers according to claim 1 , wherein
[1.32−(0.025× MOC )]≥ m≥[ 1.17−(0.025× MOC )].

4. The halogenated copolymers according to claim 1 , wherein the isobutylene content is from 85.0 to 99.5 mol.-% and the isoprene content is from 0.5 to 15.0 mol.-%.

5. The halogenated copolymers according to claim 4 , wherein the isobutylene content is 862 to 99.5 mol.-% and the isoprene content is 0.5 to 3.8 mol.-%.

6. The halogenated copolymers according to claim 1 , wherein an amount of halogen of the halogenated copolymers is 0.1 to 8.0 wt.-%, by weight of the halogenated copolymer.

7. A process for the preparation of copolymers of isobutylene and isoprene having a copolymer sequence distribution defined by equation (I)
F=mA /(1 −mA ) 2   (eq. I)

wherein
A is the molar ratio of isoprene to isobutylene in the copolymer as determined by 1 H NMR; and
F is the isoolefin-isoprene-isoprene triad fraction in the copolymer as determined by 13 C NMR; and
m is in the range of
[1.35−(0.03× MOC )]≥ m≥[ 1.15−(0.03× MOC )]

whereby MOC is the content of isoprene in the copolymer in mol-% as determined by 1 H NMR,

the process comprising:
polymerizing monomers of a monomer mixture comprising isobutylene monomers and isoprene monomers, in a diluent at a mass ratio of monomer mixture to diluent of 5:96 to 95:5, and in the presence of an initiator system to form a copolymer solution comprising the copolymer, the diluent and residual monomers of the monomer mixture; and
separating the residual monomers of the monomer mixture and the diluent from the copolymer solution to obtain the copolymer,
whereby the polymerizing is carried out
at a temperature of −100 to 0° C., and

whereby the diluent
comprises at least 50.0 wt.-% of 2,3,3,3-tetrafluoro-1-propene.

8. The process according to claim 7 , wherein for the diluent the content of aliphatic hydrocarbons having a boiling point of 5° C. to 95° C. at a pressure of 1013 hPa and being linear (n-alkenes) does not exceed 85 wt.-%.

9. The process according to claim 7 , wherein for the diluent the content of cyclic hydrocarbons having a boiling point of 5° C. to 95° C. at a pressure of 1013 hPa does not exceed 25 wt.-%.

10. The process according to claim 7 , wherein the initiator system comprises ethyl aluminum sesquichloride.

11. The process according to claim 7 , wherein for the initiator system water and/or alcohols is used as proton source.

12. The process according to claim 7 , wherein the copolymers are halogenated and after separating the residual monomers and the diluent from the copolymer solution to obtain the copolymers, the process further comprises halogenation of the copolymers.

13. The process according to claim 12 , wherein the halogenation is carried out using elemental chlorine (Cl 2 ) or bromine (Br 2 ) as halogenation agent.

14. A polymer product comprising the halogenated copolymers according to claim 1 , either cured or uncured.

15. The halogenated copolymers according to claim 1 , wherein the isobutylene content is 36.3 to 99.0 mol.-% and the isoprene content is from 1.0 to 3.7 mol.-%.

16. The halogenated copolymers according to claim 1 , wherein an amount of halogen of such halogenated copolymers is 1.8 to 2.3 wt.-% of the total weight of the halogenated copolymer.

17. The halogenated copolymers according to claim 1 , wherein the isobutylene content is 88M to 99.0 mol.-% and the isoprene content is 1.0 to 12.0 mol.-%.

18. The halogenated copolymers according to claim 1 , wherein an amount of halogen of the halogenated copolymers is 0.8 to 3 wt.-%, by weight of the halogenated copolymer.

19. The process according to claim 7 , wherein the diluent comprises at least 90.0 wt.-% of 2,3,3,3-tetrafluoro-1-propene.

20. The process according to claim 7 , wherein the diluent comprises at least 98.0 wt.-% of 2,3,3,3-tetrafluoro-1-propene.

Assignees

• Arlanxeo Singapore Pte Ltd

Inventors

• Nguyen Paul
• Teertstra Steven John
• Watson Jessica

Classifications

• C08F2/04

  Polymerisation in solution (C08F2/32 takes precedence) · CPC title

• C08F210/12 Primary

  with conjugated diolefins, e.g. butyl rubber · CPC title

• C08F6/06

  Treatment of polymer solutions {(C08F6/001, C08F6/006, C08F6/008, C08F6/02, C08F6/04 take precedence)} · CPC title

• C08F8/22

  by reaction with free halogens · CPC title

• C08C19/14

  by reaction with halogens · CPC title