High melt strength polypropylene and methods of making same

Patent metadata

Field	Value
Publication number	US-9890226-B2
Application number	US-201514791890-A
Country	US
Kind code	B2
Filing date	Jul 6, 2015
Priority date	Feb 24, 2011
Publication date	Feb 13, 2018
Grant date	Feb 13, 2018

Abstract

A high melt strength polypropylene is formed using maleated polypropylene and a combination of coupling agents and acid neutralizers. The maleated polypropylene can be formed using multi-functional monomers. The high melt strength polypropylene can be useful for foaming, sheet extrusion thermoforming, extrusion blow molding, extrusion coating, fiber, film, and the like.

First claim

What is claimed:

1. A method of making a high melt strength polypropylene ionomer, comprising:
reactively blending a combination of a functionalized polypropylene, from 0.5 to 1.0 weight percent water, from 0.5 to 10 weight percent of an acid neutralizer, and an amine coupling agent, and
recovering a polypropylene product of enhanced melt strength.

2. The method of claim 1 , wherein the functionalized polypropylene is maleated polypropylene, that is formed by the reactive extrusion of a peroxide, maleic anhydride, and 0.1 to 5% by weight of a multi-functional monomer.

3. The method of claim 2 , wherein the multi-functional monomer is chosen from the group consisting of di- and tri-acrylates.

4. The method of claim 1 , wherein the amine coupling agent is 1,3-phenylenediamine.

5. The method of claim 1 , wherein the acid neutralizer is a metal salt.

6. The method of claim 1 , wherein the acid neutralizer is chosen from the group consisting of: potassium hydroxide, zinc stearate, zinc acetate, sodium hydroxide, and combinations thereof.

7. The method of claim 1 , wherein the step of reactive blending comprises reactively blending a combination of the functionalized polypropylene, the amine coupling agent, the water, the acid neutralizer and an ionic monomer.

8. A method comprising:
reactively blending a functionalized polypropylene with an amine coupling agent, an acid neutralizer, or combinations thereof, wherein the reactively blending comprises reactively blending a combination of the functionalized polypropylene, the acid neutralizer, and from 0.5 to 1 percent by weight of water; and
recovering a polypropylene product.

9. The method of claim 8 , wherein the step of reactively blending comprises reactively blending a combination of the functionalized polypropylene and the acid neutralizer, and wherein the polypropylene product is a polypropylene ionomer.

10. The method of claim 8 , wherein the functionalized polypropylene is maleated polypropylene that is formed by the reactive extrusion of a peroxide, maleic anhydride, and 0.1 to 5% by weight of a multi-functional monomer, wherein the step of reactively blending comprises reactively blending a combination of the functionalized polypropylene and the acid neutralizer, and wherein the polypropylene product is a polypropylene ionomer.

11. The method of claim 8 , wherein the functionalized polypropylene is maleated polypropylene that is formed by the reactive extrusion of a polypropylene, a peroxide, and maleic anhydride, and wherein the step of reactively blending comprises reactively blending a combination of the functionalized polypropylene and the amine coupling agent.

12. The method of claim 8 , wherein the functionalized polypropylene is maleated polypropylene that is formed by the reactive extrusion of a polypropylene, a peroxide, maleic anhydride, and a multi-functional monomer, and wherein the step of reactively blending comprises reactively blending a combination of the functionalized polypropylene and the amine coupling agent.

13. The method of claim 8 , wherein the functionalized polypropylene is maleated polypropylene that is formed by the reactive extrusion of a polypropylene, a peroxide, maleic anhydride, and a multi-functional monomer, wherein the step of reactively blending comprises reactively blending a combination of the functionalized polypropylene, the amine coupling agent, and the acid neutralizer, and wherein the polypropylene product is a polypropylene ionomer.

14. The method of claim 8 , further comprising blending the polypropylene product with a polymer resin, wherein the polypropylene product comprises a multi-functional monomer, the acid neutralizer, or both.

15. The method of claim 14 , wherein the polymer resin is a polypropylene homopolymer or a polypropylene impact copolymer.

16. The method of claim 8 , wherein the functionalized polypropylene is formed by reactively extruding polypropylene, a free radical initiator, and a graftable monomer.

17. The method of claim 16 , wherein the polypropylene is a homopolymer, or wherein the polypropylene is a copolymer containing at least 50 percent by weight of polypropylene, wherein a remaining portion a C 2 -C 20 olefin.

18. The method of claim 16 , wherein the polypropylene has a crystallinity of at least 30% and a stereoregularity of at least 60%.

19. The method of claim 16 , wherein the polypropylene is isotactic or syndiotactic, and has a melt flow index of from 0.1 to 100 g/10 min., as measured according to ASTM D 1238 at 230° C. under a load of 2.16 kg.

20. The method of claim 16 , wherein the polypropylene is an impact copolymer.

21. The method of claim 20 , wherein the impact copolymer has a density ranging from 0.88 to 0.93 g/cm 3 , a melting point ranging from 155 to 170° C., and a melt flow rate ranging from 0.1 to 40 g/10 min.

22. The method of claim 16 , wherein the graftable monomer is present in an amount ranging from 0.01 to 10% by weight with respect to the polypropylene, and contains a carbonyl, carboxylic acid or acid anhydride functional group.

23. The method of claim 22 , wherein the graftable monomer is acrylic acid, methacrylic acid, maleic acid, fumaric acid, itaconic acid, crotonic acid, citraconic acid, maleic anhydride, itaconic anhydride, crotonic anhydride and citraconic anhydride, maleic anhydride, or allyl methacrylate.

24. The method of claim 8 , wherein the functionalized polypropylene is reactively blended with the acid neutralizer, wherein the acid neutralizer is a metal salt, wherein a cationic portion of the metal salt is an alkali cation, an alkaline-earth cation, or a transition-metal cation, wherein an anionic portion of the metal salt is an alcoholate, carboxylate, hydroxide, oxide, alkyl, carbonate, or hydrogen-carbonate, and wherein the polypropylene product is a polypropylene ionomer.

25. The method of claim 24 , wherein the acid neutralizer is sodium hydroxide, calcium oxide, sodium carbonate, sodium hydrogencarbonate, sodium methoxide, sodium acetate, magnesium ethoxide, diethylzinc, aluminum butoxide, zirconium butoxide, potassium hydroxide, zinc acetate, or zinc stearate.

26. The method of claim 8 , wherein the amine coupling agent is present in an amount ranging from 0.1 to 5 weight percent.

27. The method of claim 26 , wherein the amine coupling agent is a C 4 -C 12 alkylene diamine.

28. The method of claim 26 , wherein the amine coupling agent is hexamethylene diamine (HMDA), polypropylene glycol)-bis-(2-propylamine), dodecamethylenediamine, or 1,3-phenylenediamine.

29. The method of claim 8 , wherein the reactively blending comprises reactively extruding at a temperature of from 150 to 300° C.

30. The method of claim 8 , wherein the polypropylene product has a melt flow rate of from 0.001 to 60 g/10 min.

31. The method of claim 8 , further comprising subjecting the polypropylene product to a plastics shaping process to obtain an article, wherein the plastics shaping process is foaming, sheet extrusion thermoforming, extrusion blow molding, extrusion coating, blow molding, injection blow molding, injection stretch blow molding, or thermoforming.

32. The method of claim 8 , wherein the functionalized polypropylene includes 0.1 to 10% by weight of a multi-functional monomer, wherein the multi-functional monomer is an a

Assignees

• Fina Technology

Inventors

• Li Fengkui
• Ashbaugh John
• Rauscher David
• Dotter Robert

Classifications

• C08J9/00

  Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof (mechanical aspects of shaping of plastics or substances in a plastic state for the production of porous or cellular articles B29C) · CPC title

• C08F10/06 Primary

  Propene · CPC title

• C08L23/26 Primary

  modified by chemical after-treatment (saponified copolymers C08L23/0861; unsaturated acid salts C08L23/0876) · CPC title