IP Library Granted Patent US 12,202,180
Granted Patent B2
US 12,202,180 · App. 17/607,059 · Granted Jan 21, 2025

Process for preparing a cap or closure

Inventors: Jingbo Wang (Linz, AT); Markus Gahleitner (Linz, AT); Elisabeth Potter (Linz, AT); Luc Monnissen (Arsimont, BE); Meta Cigon (Vienna, AT); Daniela Mileva (Linz, AT)
Assignee: Borealis AG
B29C45/0001B29C45/7207B29C48/00C08F110/06B29C45/46B29K2023/12B29L2031/56
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,202,180
App. No.
17/607,059
Granted
Jan 21, 2025
Kind
B2
Abstract

A process for producing a cap or closure comprising obtaining a polypropylene composition by sequential polymerization comprising the steps: A) polymerizing in a first reactor, preferably a slurry reactor, in the presence of a Ziegler-Natta catalyst monomers comprising propylene and optionally one or more comonomers selected from ethylene and C4-C10 alpha-olefins, to obtain a first propylene polymer fraction having a comonomer content in the range of 0.0 to 1.8 wt %, and a MFR2 in the range of from 12.0 to 40.0 g/10 min, as measured according to ISO 1133 at 230° C. under a load of 2.16 kg; B) polymerizing in a second reactor, preferably a first gas-phase reactor, monomers comprising propylene and one or more comonomers selected from ethylene and C4-C10 alpha-olefins, in the presence of the first propylene polymer fraction, to obtain a second propylene polymer fraction, wherein the polypropylene composition comprising said first and second propylene polymer fractions has an MFR2 in the range of from 12.0 to 60.0 g/10 min, as measured according to ISO 1133 at 230° C. under a load of 2.16 kg, has a comonomer content in the range of from 2.2 to 5.0 wt % and wherein the ratio of the comonomer content of component A) to the comonomer content of the polypropylene composition is 0.35 or less, C) melting, extruding and moulding the polypropylene composition in the presence of at least one nucleating agent to prepare a cap or closure; and D) exposing the cap or closure obtained in step (C) to a cooling rate of 50 K/s or more.

Claims (37)

1. A process for producing a cap or closure comprising obtaining a polypropylene composition by sequential polymerization comprising the steps:

A) polymerizing in a first reactor, in the presence of a Ziegler-Natta catalyst, monomers comprising propylene and optionally one or more comonomers selected from ethylene and C4-C10 alpha-olefins, to obtain a first propylene polymer fraction having a comonomer content in the range of 0.0 to 1.8 wt %, and a MFR2 in the range of from 12.0 to 40.0 g/10 min, as measured according to ISO 1133 at 230° C. under a load of 2.16 kg;

B1) polymerizing in a second reactor, monomers comprising propylene and one or more comonomers selected from ethylene and C4-C10 alpha-olefins, in the presence of the first propylene polymer fraction, to obtain a second propylene polymer fraction,

wherein the polypropylene composition comprising said first and second propylene polymer fractions and optionally a third propylene polymer fraction has an MFR2 in the range of from 12.0 to 60.0 g/10 min, as measured according to ISO 1133 at 230° C. under a load of 2.16 kg, has a comonomer content in the range of from 2.2 to 5.0 wt % and wherein the ratio of the comonomer content of the first propylene polymer fraction to the comonomer content of the polypropylene composition is 0.35 or less,

C) melting, extruding and moulding the polypropylene composition in the presence of at least one nucleating agent to prepare a cap or closure; and

D) exposing the cap or closure obtained in step (C) to a cooling rate of 50K/s or more.

2. The process as claimed in claim 1 further comprising, after step A and B1, and before step C) and D),

(B2) polymerizing in a third reactor, monomers comprising propylene and one or more comonomers selected from ethylene and optionally C4-C10 alpha olefins, in the presence of the second propylene polymer fraction to obtain the third propylene polymer fraction.

3. The process of claim 1 , wherein the polymerization is carried out in the presence of a Ziegler-Natta catalyst which is free of a phthalic compound.

4. The process of claim 1 , wherein the one or more comonomers are selected from solely ethylene.

5. The process of claim 1 , wherein the comonomer content of the polypropylene composition is in the range of 2.2 to 4.5 wt %.

6. The process of claim 1 , wherein the at least one nucleating agent is present in the range of from 0.01 to 1.0 wt %, relative to the total amount of polypropylene composition.

7. The process of claim 1 , wherein said polypropylene composition has

a crystallisation temperature (Tc) of at least 55° C. when subjected to a cooling rate of 100 K/s; and

a crystallisation temperature (Tc) of at least 40° C. when subjected to a cooling rate of 300 K/s.

8. The process of claim 1 , wherein the cooling rate is 100 to 600 K/s.

9. The process of claim 1 , wherein the melting step is effected at a temperature of at least 200° C.

10. The process of claim 1 , wherein the moulding in step C) is effected in a mould and after cooling step D), the cap or closure is ejected from the mould and a new cap or closure is then formed in the mould and subjected to cooling step D).

11. The process of claim 10 , wherein the cycle time for each cap to be moulded, cooled, and ejected from the mould is 6.0 secs or less.

12. The cap or closure obtained by the process of claim 1 .

13. The process of claim 2 , wherein the moulding in step C) is effected in a mould and after cooling step D), the cap or closure is ejected from the mould and a new cap or closure is then formed in the mould and subjected to cooling step D).

14. The process of claim 13 , wherein the cycle time for each cap to be moulded, cooled, and ejected from the mould is 6.0 secs or less.

15. The cap or closure is obtained by the process of claim 2 .

16. The process of claim 1 , wherein the first reactor is a slurry reactor and/or the second reactor is a first gas-phase reactor.

17. The process of claim 2 , wherein the first reactor is a slurry reactor and/or the second reactor is a first gas-phase reactor, and/or the third reactor is a third gas-phase reactor.

18. A cap or closure comprising a polypropylene composition and at least one nucleating agent, wherein said polypropylene composition having a first homo or copolymer fraction, a second copolymer fraction and optionally a third copolymer fraction, said polypropylene composition having an ethylene content of 2.2 to 5.0 wt % and wherein said polypropylene composition has

a crystallisation temperature (Tc) of at least 90° C. when subjected to a cooling rate of 10 K/s;

a crystallisation temperature (Tc) of at least 55° C. when subjected to a cooling rate of 100 K/s; and

a crystallisation temperature (Tc) of at least 40° C. when subjected to a cooling rate of 300 K/s.

19. The cap or closure of claim 18 , wherein the polypropylene composition has an MFR2 in the range of from 12.0 to 60.0 g/10 min, as measured according to ISO 1133 at 230° C. under a load of 2.16 kg, and wherein the ratio of the comonomer content of the first homo or copolymer fraction to the comonomer content of the polypropylene composition is 0.35 or less.

20. The cap or closure as claimed in claim 18 , wherein said polypropylene composition comprises the first homo or copolymer fraction, the second copolymer fraction and the third copolymer fraction.

21. A process for producing a cap or closure comprising obtaining a first polypropylene composition comprising a nucleating agent and a second polypropylene composition having a first homo or copolymer fraction, a second copolymer fraction and optionally a third copolymer fraction, wherein said second polypropylene composition having an ethylene content of 2.2 to 5.0 wt % and, wherein said second polypropylene composition has

a crystallisation temperature (Tc) of at least 90° C. when subjected to a cooling rate of 10 K/s;

a crystallisation temperature (Tc) of at least 55° C. when subjected to a cooling rate of 100 K/s; and

a crystallisation temperature (Tc) of at least 40° C. when subjected to a cooling rate of 300 K/s;

melting, extruding and moulding the second polypropylene composition in the presence of the at least one nucleating agent to prepare a cap or closure; and

exposing the cap or closure obtained to a cooling rate of 100K/s or more.

Assignments (2)
CHANGE OF ADDRESS Recorded Feb 23, 2022
From: BOREALIS AG
To: BOREALIS AG
Reel/Frame 059219/0949 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 29, 2021
From: WANG, JINGBO; GAHLEITNER, MARKUS; POTTER, ELISABETH; MONNISSEN, LUC; CIGON, META; MILEVA, DANIELA
To: BOREALIS AG
Reel/Frame 058228/0564 →
Priority Claims (1)
EP 19171610 · Apr 29, 2019 · regional
Continuity (1)
Related Publication 20220227030A1 · Jul 21, 2022
References Cited (48)
CN 102532711A · 2012 [cited by applicant]
CN 104797652A · 2015 [cited by applicant]
EA 014272B1 · 2010 [cited by applicant]
EP 0339804 · 1997 [cited by applicant]
EP 0860457 · 2003 [cited by applicant]
EP 0887379 · 2004 [cited by applicant]
EP 2625223 · 2013 [cited by applicant]
EP 3006472 · 2016 [cited by applicant]
EP 2686382 · 2016 [cited by applicant]
EP 2898017 · 2017 [cited by applicant]
EP 2610272 · 2017 [cited by applicant]
EP 2610271 · 2019 [cited by applicant]
RU 2637911C2 · 2017 [cited by applicant]
WO 1999024478 · 1999 [cited by applicant]
WO 1999024479A1 · 1999 [cited by applicant]
WO 2004000899 · 2003 [cited by applicant]
WO 2004111095 · 2004 [cited by applicant]
WO 2007057142A1 · 2007 [cited by applicant]
WO 2007093376A1 · 2007 [cited by applicant]
WO 2009021686 · 2009 [cited by applicant]
WO 2011071718A2 · 2011 [cited by applicant]
WO 2012007430 · 2012 [cited by applicant]
WO 2012126759 · 2012 [cited by applicant]
WO 2014154610 · 2014 [cited by applicant]
WO 2014187687 · 2014 [cited by applicant]
WO 2014199271A1 · 2014 [cited by applicant]
WO 2016055361 · 2016 [cited by applicant]
WO 2016116606 · 2016 [cited by applicant]
WO 2016135107 · 2016 [cited by applicant]
WO 2016135108 · 2016 [cited by applicant]
WO 2019002345 · 2019 [cited by applicant]
WO 2019002346 · 2019 [cited by applicant]
WO 2019048529A1 · 2019 [cited by applicant]
WO 2019115510 · 2019 [cited by applicant]
Lin, “Research on Influence of Nucleating Agent on Injection Molding Cycle of Polypropylene,” Home Appliance, Sep. 2017, p. 42-43. [cited by applicant]
International Search Report and Written Opinion in PCT/EP2020/061795. Mailed Jul. 20, 2020. 14 pages. [cited by applicant]
Busico, Vincenzo, et al. “Alk-1-ene Polymerization in the Presence of a Monocyclopentadienyl Zirconium (iv) Acetamidinate Catalyst: Microstructural and Mechanistic Insights.” Macromolecular rapid communications 28.10 (2… [cited by applicant]
Chemical Abstracts, Columbus, Ohio, US; abstract No. 135861-56-2. [cited by applicant]
Cheng, H. N. “Carbon-13 NMR analysis of ethylene-propylene rubbers.” Macromolecules 17.10 (1984): 1950-1955. [cited by applicant]
Del Hierro, et al. “Soluble Fraction Analysis in polypropylene”, The Column Advanstar Publications, Feb. 2014 (Feb. 1, 2014), pp. 18-23. [cited by applicant]
Iervolino, E., et al. “Temperature calibration and electrical characterization of the differential scanning calorimeter chip UFS1 for the Mettler-Toledo Flash DSC 1.” Thermochimica acta 522.1-2 (2011): 53-59. [cited by applicant]
Mathot, Vincent, et al. “The Flash DSC 1, a power compensation twin-type, chip-based fast scanning calorimeter (FSC): First findings on polymers.” Thermochimica Acta 522.1-2 (2011): 36-45. [cited by applicant]
Mileva, Daniela, Davide Tranchida, and Markus Gahleitner. “Designing polymer crystallinity: An industrial perspective.” Polymer Crystallization 1.2 (2018): e10009. [cited by applicant]
Rhoades, Alicyn Marie, et al. “Effect of cooling rate on crystal polymorphism in beta-nucleated isotactic polypropylene as revealed by a combined WAXS/FSC analysis.” Polymer 90 (2016): 67-75. [cited by applicant]
Singh, Gurmeet, Ajay V. Kothari, and Virendra K. Gupta. “Triad sequence determination of ethylene-propylene copolymers-application of quantitative 13C NMR.” Polymer Testing 28.5 (2009): 475-479. [cited by applicant]
Van Drongelen, Martin, et al. “Microfocus wide-angle X-ray scattering of polymers crystallized in a fast scanning chip calorimeter.” Thermochimica acta 563 (2013): 33-37. [cited by applicant]
Wang, Wen-Jun, and Shiping Zhu. “Structural analysis of ethylene/propylene copolymers synthesized with a constrained geometry catalyst.” Macromolecules 33.4 (2000): 1157-1162. [cited by applicant]
Zhou, Zhe, et al. “A new decoupling method for accurate quantification of polyethylene copolymer composition and triad sequence distribution with 13C NMR.” Journal of Magnetic Resonance 187.2 (2007): 225-233. [cited by applicant]