Quantitative preparation of allyl telechelic polyisobutylene under reflux conditions

US10329361B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10329361-B2
Application numberUS-201715795638-A
CountryUS
Kind codeB2
Filing dateOct 27, 2017
Priority dateOct 28, 2016
Publication dateJun 25, 2019
Grant dateJun 25, 2019

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  1. Title

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  2. Abstract

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

In one or more embodiments, the present invention provides a method for forming allyl telechelic polyisobutylene polymers having well defined molecular weights and molecular weight distributions using living cationic polymerization under ideal temperature control using a mixture of polar and nonpolar refluxing solvents. The methods according to various embodiments of the present invention provide temperature control that approaches the ideal, i.e., the heat of polymerization is instantaneously absorbed by the medium and the temperature of the system remains unchanged. The heat generated during the exothermic polymerization of isobutylene is released as an increase in the rate of reflux, rather than the temperature, since the temperature is set by the boiling point of the system and does not change.

First claim

Opening claim text (preview).

What is claimed is: 1. A method for making polyisobutylene by living cationic polymerization of isobutylene comprising: A) providing an externally cooled reaction vessel; B) charging said externally cooled reaction vessel with isobutylene, an initiator, a refluxing solvent mixture, and a proton trap or electron donor at a temperature below a boiling point for said refluxing solvent mixture; C) allowing the temperature of the externally cooled reaction vessel to increase to the boiling point of said refluxing solvent mixture causing the refluxing solvent mixture to reflux; D) inducing living cationic polymerization of the isobutylene by the addition of a co-initiator to said externally cooled reaction vessel to produce polyisobutylene polymer chains; and E) terminating the living cationic polymerization reaction to produce the polyisobutylene polymer. 2. The method of claim 1 wherein said refluxing solvent mixture comprises a polar solvent and a nonpolar solvent. 3. The method of claim 2 wherein said nonpolar solvent is propane. 4. The method of claim 2 wherein said nonpolar polar solvent is methyl chloride (CH 3 Cl) or dichloromethane (CH 2 Cl 2 ). 5. The method of claim 1 wherein said refluxing solvent mixture has a boiling point of about −40° C. 6. The method of claim 4 wherein volume ratio of propane to methyl chloride in said refluxing solvent mixture is from about 9:1 to about 1:9. 7. The method of claim 4 wherein the ratio of propane to methyl chloride in said refluxing solvent mixture by volume is from about 3:2 to about 7:3. 8. The method of claim 1 wherein the living cationic polymerization reaction is allowed to continue for about 15 minutes or until substantially all of the isobutylene has been reacted before the step of termination (step E). 9. The method of claim 1 wherein the step of terminating the polymerization reaction (step E) comprises adding a termination agent, wherein said termination agent terminates the living cationic polymerization reaction by reacting with said polyisobutylene chains to leave terminal allyl functional groups on said polyisobutylene chains. 10. The method of claim 9 wherein the polyisobutylene polymer produced in step E has a molecular weight distribution of from 1.0 to 1.2 and a number average end functionalization (∫ n ) of from about 1.8 to about 2.0. 11. A method for controlling the temperature for conducting living cationic polymerization of isobutylene above −78° C. comprising: A) providing an externally cooled reaction vessel; B) charging said externally cooled reaction vessel with isobutylene, an initiator, a refluxing solvent mixture, and a proton trap at a temperature below a boiling point for said refluxing solvent mixture, wherein said refluxing solvent mixture comprises a polar solvent and a nonpolar solvent; C) allowing the temperature of the externally cooled reaction vessel to increase to the boiling point of said refluxing solvent mixture causing the refluxing solvent mixture to reflux; D) inducing living cationic polymerization of the isobutylene by the addition of a co-initiator to said externally cooled reaction vessel to produce polyisobutylene polymer chains; wherein the temperature inside said externally cooled reaction vessel is maintained at or about said boiling point during said living cationic polymerization. 12. The method of claim 11 wherein said nonpolar solvent is propane and said polar solvent is methyl chloride. 13. The method of claim 12 wherein said refluxing solvent mixture comprises from about 60% to about 70% propane and from about 30% to about 40% methyl chloride by volume. 14. A method of making a di-telechelic allyl-functionalized polyisobutylene by living cationic polymerization of isobutylene comprising: A) providing an externally cooled reaction vessel equipped with a reflux condenser; B) charging said externally cooled reaction vessel with isobutylene, a bi-functional initiator, a refluxing solvent mixture comprising propane and methyl chloride, and a proton trap at a temperature below a boiling point for said refluxing solvent mixture; C) allowing the temperature of the externally cooled reaction vessel to increase to the boiling point of said refluxing solvent mixture causing the refluxing solvent mixture to reflux; D) inducing living cationic polymerization of the isobutylene by the addition of a co-initiator to said externally cooled reaction vessel to produce polyisobutylene polymer chains; E) allowing living cationic polymerization to continue until substantially all of the isobutylene has been reacted; F) terminating the living cationic polymerization reaction by adding a termination agent, wherein said termination agent terminates the living cationic polymerization reaction by reacting with said polyisobutylene chains to leave terminal allyl functional groups on said polyisobutylene chains to produce the di-telechelic allyl-functionalized polyisobutylene. 15. The method of claim 14 wherein said refluxing solvent mixture has a boiling point of about −40° C. 16. The method of claim 14 wherein said bi-functional initiator comprises 1-(tert-butyl)-3,5-bis(2-chloropropan-2-yl)benzene (HDCCl). 17. The method of claim 14 wherein the step of terminating (step F) is performed about 15 minutes after the step inducing (step C). 18. The method of claim 14 wherein the step of terminating (step F) is performed not more than 5 minutes after all of the isobutylene has reacted. 19. The method of claim 14 wherein said refluxing solvent mixture comprises from about 60% to about 70% propane and from about 30% to about 40% methyl chloride by volume. 20. The method of claim 14 wherein the di-telechelic allyl-functionalized polyisobutylene produced in step F has a molecular weight distribution of from about 1.0 to about 1.2 and a number average end functionalization (∫ n ) of from about 1.8 to about 2.0.

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Inventors

Classifications

  • Broad molecular weight distribution, i.e. Mw/Mn > 6 · CPC title

  • C08F110/10Primary

    Isobutene · CPC title

  • taking place solely at one end or both ends of the polymer backbone, i.e. not in the side or lateral chains · CPC title

  • containing six-membered aromatic rings · CPC title

  • leading to the formation or introduction of aliphatic or alicyclic unsaturated groups · CPC title

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What does patent US10329361B2 cover?
In one or more embodiments, the present invention provides a method for forming allyl telechelic polyisobutylene polymers having well defined molecular weights and molecular weight distributions using living cationic polymerization under ideal temperature control using a mixture of polar and nonpolar refluxing solvents. The methods according to various embodiments of the present invention provi…
Who is the assignee on this patent?
Kennedy Joseph P, Deodhar Tejal J, Keszler Balazs L, and 1 more
What technology area does this patent fall under?
Primary CPC classification C08F110/10. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jun 25 2019 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).