Enhanced heat stability polypropylene

US11780939B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11780939-B2
Application numberUS-202016795790-A
CountryUS
Kind codeB2
Filing dateFeb 20, 2020
Priority dateFeb 20, 2019
Publication dateOct 10, 2023
Grant dateOct 10, 2023

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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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Abstract

Official abstract text for this publication.

A process forming a high MFR polypropylene includes providing a reactor powder polypropylene, the reactor powder polypropylene having a melt flow rate of less than 100 dg/min. The process also includes mixing the reactor powder polypropylene with a free-radical initiator to form a powder/initiator mixture and subjecting the powder/initiator mixture to post-reactor forming. The present disclosure further provides for a vis-broken polypropylene and a polymer article.

First claim

Opening claim text (preview).

What is claimed is: 1. A process for forming a high melt flow rate (MFR) polypropylene comprising: providing a reactor powder polypropylene, wherein the reactor powder polypropylene comprises a nucleator comprising talc, and wherein the reactor powder polypropylene has a MFR of less than 100 dg/min as determined by ASTM D1238; mixing the reactor powder polypropylene with a free-radical initiator to form a powder/initiator mixture; and subjecting the powder/initiator mixture to post-reactor forming to form discrete particle comprising a vis-broken polypropylene as the high MFR polypropylene, wherein the vis-broken polypropylene has a MFR greater than the MFR of the reactor powder polypropylene and in a range of from 80 dg/min to 150 dg/min. 2. The process of claim 1 , wherein the reactor powder polypropylene is a homopolymer, a random copolymer, or an impact copolymer. 3. The process of claim 1 , wherein the reactor powder polypropylene has a MFR greater than or equal to 10 and less than 100 dg/min as measured by ASTM D1238. 4. The process of claim 1 , wherein the nucleator further comprises silica, a metallic-silicate hydrate, an organic derivative of dibenzylidene sorbitol, a sorbitol acetal, or a combination thereof. 5. The process of claim 1 , wherein the free radical initiator is an organic peroxide. 6. The process of claim 5 , wherein organic peroxide is 3,6,9-triethyl-3,6,9-trimethyl-1,4,7-triperoxonane, or 2,5-bis(tert-butylperoxy)-2,5-dimethylhexane. 7. The process of claim 6 , wherein the organic peroxide is 3,6,9-triethyl-3,6,9-trimethyl-1,4,7-triperoxonane and no 2,5-bis(tert-butylperoxy)-2,5-dimethylhexane is present. 8. The process of claim 5 , wherein an amount of organic peroxide present in the powder/initiator mixture is between 50 ppm to 1500 ppm. 9. The process of claim 1 , wherein a ratio of MFR of the vis-broken polypropylene to the reactor powder polypropylene is between 1.25:1 to 25:1. 10. The process of claim 9 , wherein the ratio of MFR of the vis-broken polypropylene to the reactor powder polypropylene is between 2.5:1 to 12:1. 11. The process of claim 1 , wherein the powder/initiator mixture is combined with a secondary antioxidant. 12. The process of claim 11 , wherein the secondary antioxidant is a phosphite, hindered amine stabilizer or hydroxylamine. 13. The process of claim 12 , wherein the secondary antioxidant is present in the powder/initiator mixture in an amount between 0.1% to 3 wt %. 14. The process of claim 1 , wherein, following post-reactor forming, a TGA of the high MFR polypropylene at 230° C. has a 2% loss in weight of between 75 minutes and 200 minutes. 15. The process of claim 14 , wherein, following post-reactor forming, the TGA of the high MFR polypropylene at 230° C. has a 3% loss in weight of between 77 minutes and 210 minutes. 16. The process of claim 1 , wherein the post-reaction forming is accomplished by extrusion into pellets, compaction into a fused/physically bonded pellet, prill bead manufacturing, pastillation, or melt atomization. 17. A vis-broken polypropylene obtained by the process of claim 1 . 18. The process of claim 1 further comprising forming the discrete particle into an article. 19. The process of claim 18 , wherein the article is a motor vehicle component, appliance, or filter media. 20. A polymer article formed from the vis-broken polypropylene of claim 1 . 21. The process of claim 1 , wherein the MFR of the high MFR polypropylene is in a range of from about 100 dg/min to 150 dg/min. 22. A process for forming a high melt flow rate (MFR) polypropylene comprising: providing a reactor powder polypropylene, the reactor powder polypropylene comprising a nucleator and having a MFR of less than 100 dg/min as determined by ASTM D1238; mixing the reactor powder polypropylene with a free-radical initiator to form a powder/initiator mixture; and subjecting the powder/initiator mixture to post-reactor forming to form discrete particle comprising a vis-broken polypropylene as the high MFR polypropylene, wherein the vis-broken polypropylene has a MFR greater than the MFR of the reactor powder propylene and in a range of from 80 dg/min to 150 dg/min; wherein the nucleator is talc and the talc is present in the reactor powder polypropylene in an amount between 500 ppm and 20,000 ppm. 23. The process of claim 22 , wherein the MFR of the high MFR polypropylene is in a range of from about 100 dg/min to 150 dg/min. 24. A process for forming a high melt flow rate (MFR) polypropylene comprising: providing a reactor powder polypropylene, the reactor powder polypropylene having a MFR of less than 100 dg/min as determined by ASTM D1238; mixing the reactor powder polypropylene with a free-radical initiator to form a powder/initiator mixture; and subjecting the powder/initiator mixture to post-reactor forming to form discrete particle comprising a vis-broken polypropylene as the high MFR polypropylene, wherein the vis-broken polypropylene has a MFR greater than the MFR of the reactor powder polypropylene and in a range of from 80 dg/min to 150 dg/min; wherein the powder/initiator mixture is combined with talc. 25. The process of claim 24 , wherein the MFR of the high MFR polypropylene is in a range of from about 100 dg/min to 150 dg/min.

Assignees

Inventors

Classifications

  • C08F10/06Primary

    Propene · CPC title

  • characterised by structure or composition · CPC title

  • Silicon-containing compounds · CPC title

  • Stabilisers against oxidation, heat, light, ozone · CPC title

  • Peroxides · CPC title

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What does patent US11780939B2 cover?
A process forming a high MFR polypropylene includes providing a reactor powder polypropylene, the reactor powder polypropylene having a melt flow rate of less than 100 dg/min. The process also includes mixing the reactor powder polypropylene with a free-radical initiator to form a powder/initiator mixture and subjecting the powder/initiator mixture to post-reactor forming. The present disclosur…
Who is the assignee on this patent?
Fina Technology
What technology area does this patent fall under?
Primary CPC classification C08F10/06. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Oct 10 2023 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 6 related publications on this page (citations in our corpus or others sharing the same primary CPC).