IP Library Granted Patent US 12,577,372
Granted Patent B2
US 12,577,372 · App. 18/231,814 · Granted Mar 17, 2026

Aerated polypropylene compositions exhibiting specific emission

Inventors: Andreas Fuchs (Linz, AT); Luca Boragno (Linz, AT); Girish Suresh Galgali (Linz, AT); Markus Gahleitner (Linz, AT); Jurgen Huber (Linz, AT); Stefanie Engleder (Linz, AT)
Assignee: BOREALIS AG
C08K5/20C08K3/34C08K3/40C08L23/12C08L2205/025
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Quick Facts
Patent No.
US 12,577,372
App. No.
18/231,814
Granted
Mar 17, 2026
Kind
B2
Abstract

A process for preparing a polypropylene composition including oligomers having a semi-volatile organic condensable (FOG, VDA 278 October 2011), content of 50 ug/g to about 400 yg/g of the total polypropylene composition, and volatile organic compounds (VOC, VDA 278 October 2011) in an amount of less than 80 ug/g of the total polypropylene composition, wherein the weight ratio of the oligomers versus the volatiles is more than about 5.0, wherein the polypropylene composition has an MFRz2 (ISO 1133, 230° C., 2.16 kg) of 10 g/10 min or higher, wherein the polypropylene composition has a flexural modulus (ISO 178 on injection moulded specimens of 80×10×4 mm prepared in accordance with ISO 294-1:1996) of from 1000 to 2000 MPa, and wherein the total quantity of slip agent is at least 500 ppm.

Claims (50)

1 . A process for providing a polypropylene composition comprising:

semi-volatile organic condensable oligomers FOG in an amount of 50 μg/g to 400 μg/g of the total polypropylene composition determined according to VDA 278 October 2011, and

volatile organic compounds VOC in an amount of less than 80 μg/g of the total polypropylene composition determined according to VDA 278 October 2011,

wherein the weight ratio of said semi-volatile organic condensable oligomers versus said volatile organic compounds is more than 5.0,

wherein the polypropylene composition has an MFR 2 of 10 g/10 min or higher determined according to ISO 1133 at 230° C. and a load of 2.16 kg,

wherein the polypropylene composition has a flexural modulus, determined according to ISO 178 on injection molded specimens of 80×10×4 mm prepared in accordance with ISO 294-1:1996, of from 1000 to 6000 MPa, and

wherein the total quantity of slip agent is at least 500 ppm,

the process comprising:

blending

polypropylene,

filler,

slip agent,

optional HDPE,

optional plastomer, and

optional pigment in the presence of additives providing to obtain a blend,

and further subjecting the blend to a process comprising the steps of:

a) providing an aeration vessel having,

at least one inlet for aeration gas,

at least one outlet for exhaust gas,

an inlet for a raw polypropylene composition at the top of the aeration vessel,

an outlet for the polypropylene composition at the bottom of the aeration vessel,

wherein the polypropylene composition is present as a packed bed;

b) initiating a counter-current flow of the polypropylene composition and aeration gas,

c) by

feeding the raw polypropylene composition having

a volatile organic compound content VOC of greater than 150 μg/g determined according to VDA 278 October 2011; and

a semi-volatile organic condensable content FOG of greater than 350 μg/g determined according to VDA 278 October 2011, into said aeration vessel from the top,

feeding the aeration gas into said aeration vessel via the at least one inlet at the bottom;

withdrawing the exhaust gas via the outlet for exhaust gas;

withdrawing the aerated polypropylene composition via the outlet at the bottom of the aeration vessel,

d) maintaining said aeration gas flow for an aeration time of from 3 to 96 hours,

wherein the temperature of the gas is from 100° C. to 140° C., and wherein, the Reynolds number of the gas flow is from 5 to 150, whereby the Reynolds number for the flow of aeration gas through the packed bed is defined by formula (I)

Re=(ρ v s D )/μ  (I)

where:

ρ is the density of the aeration gas at the temperature used in kg/m 3 ,

μ is the kinematic viscosity of the aeration gas at the temperature used in kg/m s,

v s is the superficial velocity, defined as Q/A where Q is the volume flow rate of the aeration gas in m 3 /s and A is the cross sectional area in m 2 ,

D is the diameter in m of the particles; and

wherein no further slip agent is added to the composition after step d), the aeration step.

2 . The process according to claim 1 , wherein the slip agent is a fatty acid amide.

3 . The process according to claim 2 , wherein the fatty acid amide is erucamide or oleamide.

4 . The process according to claim 1 , wherein the odor rating according to VDA 277 is less than 1.

5 . The process according to claim 1 , wherein the fogging gravimetric is less than 1.1,

and/or wherein the total emissions according to VDA 270 are 3 μg carbon per g sample or less.

6 . The process according to claim 1 , wherein the polypropylene composition has an MFR 2 of from 10 to 25 g/10 min determined according to ISO 1133 at 230° C. and a load of 2.16 kg.

7 . The process according to claim 1 , wherein the polypropylene composition has a flexural modulus, determined according to ISO 178 on injection molded specimens of 80×10×4 mm prepared in accordance with ISO 294-1:1996, of from 1300 to 5000 MPa.

8 . The process according to claim 1 , wherein the blending step involves blending a heterophasic polypropylene with a further polypropylene homo- and/or copolymer.

9 . The process according to claim 1 , wherein the polypropylene composition has a flexural modulus, determined according to ISO 178 on injection molded specimens of 80×10×4 mm prepared in accordance with ISO 294-1:1996, of from 1200 to 5500 MPa.

10 . The process according to claim 1 , wherein the polypropylene composition has a puncture energy of from 20 to 60 J.

11 . The process according to claim 1 , wherein the filler is selected from the group consisting of talc, glass, and mixtures thereof.

Priority Claims (1)
EP 18203768 · Oct 31, 2018 · regional
Continuity (2)
Continuation 17289655
Related Publication 20240043657A1 · Feb 8, 2024
References Cited (37)
US 6218504B1 · Dolle et al. · 2001 [cited by applicant]
US 12281218B2 · Galgali · 2025 [cited by examiner]
US 20060217528A1 · Cousin et al. · 2006 [cited by applicant]
US 20170121432A1 · Salek et al. · 2017 [cited by applicant]
US 20170313866A1 · Wang et al. · 2017 [cited by applicant]
US 20180200921A1 · Grein · 2018 [cited by examiner]
CN 104870486A · 2015 [cited by applicant]
CN 106133003A · 2016 [cited by applicant]
EP 0887379B1 · 1998 [cited by applicant]
EP 2154190A1 · 2010 [cited by applicant]
EP 2262858B1 · 2013 [cited by applicant]
EP 3126408B1 · 2017 [cited by applicant]
GB 1272778A · 1972 [cited by applicant]
RU 2506288C2 · 2014 [cited by applicant]
RU 2635565C2 · 2017 [cited by applicant]
WO 1992012182A1 · 1992 [cited by applicant]
WO 9924478A1 · 1999 [cited by applicant]
WO 9924479A1 · 1999 [cited by applicant]
WO 2000068315A1 · 2000 [cited by applicant]
WO 2002088194A1 · 2002 [cited by applicant]
WO 2004000899A1 · 2003 [cited by applicant]
WO 2004039848A1 · 2004 [cited by applicant]
WO 2004111095A1 · 2004 [cited by applicant]
WO 2014090856A1 · 2014 [cited by applicant]
WO 2017079246A1 · 2017 [cited by applicant]
WO 2018114984A1 · 2018 [cited by applicant]
Applicant: Borealis AG, AT; Russian Application No. 2021114882/04(031534); Request of the Substantive Examination; Dec. 23, 2021; 20 pgs. [cited by applicant]
Applicant: Borealis AG; “Aerated Polypropylene Compositions Exhibiting Specific Emission Profiles”; European Patent Application No. EP18203768; Extended European Search Report; Mar. 28, 2019; 7 pgs. [cited by applicant]
Applicant: Borealis AG, AT; Russian Application No. 2021114882/04(031534); Request of the Substantive Examination; May 20, 2022; 10 pgs. [cited by applicant]
Applicant: Borealis AG; Chinese Application No. 201980071549.0; Chinese Office Action; Jul. 4, 2022; 12 pgs. [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”, Macromol. Rapid Commun. 2007, 28,1128-1137. [cited by applicant]
Cheng, et al., “13C NMR Analysis of Ethylene-Propylene Rubbers”, Macromolecules 17, 1984, 1950-1955. [cited by applicant]
Kakugo, Masahiro, et al., “13C Nmr Determination of Monomer Sequence Distribution in Ethylene-Propylene Copolymers Prepared with d-TiC13-Al(C2H5)2 Cl” Macromolecules 1982, 15, 1150-1152. [cited by applicant]
Resconi, Luigi, et al., “Selectivity in Propane Polymerization With Metallocene Catalysts”, Chem. Rev. 2000, 100, 1253-1345. [cited by applicant]
Singh, Gurmeet, et al., “Triad Sequence Determination of Ethylene-Propylene Copolymers—Application of Quantitative 13C NMR”, Polymer Testing 28 (2009) 475-479. [cited by applicant]
Wang, Wen-Jun, et al., “Structural Analysis of Ethylene/Propylene Copolymers Synthesized With a Constrained Geometry Catalyst”, Macromolecules 2000, 33, 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 (2007) 225-233. [cited by applicant]