# US 9,040,633 B2 · Impact-modified polypropylene > Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt - Number: US 9,040,633 B2 - Document ID: US9040633B2 - Status: Granted - Kind: B2 - Application number: 12/734,368 - Filed: 2008-10-27 - Published: 2010-10-07 - Granted: 2015-05-26 - Earliest claimed: 2007-10-31 - Assignees: Borealis Technology Oy - Applicants: Klaus Bernreitner; Tung Pham; Jens Reussner - Inventors: Klaus Bernreitner; Tung Pham; Jens Reussner - Web page: https://patentgrep.com/patent/US9040633B2 ## CPC - C08L 23/0815: {with aliphatic 1-olefins containing one carbon-to-carbon double bond} - C08L 9/00: Compositions of homopolymers or copolymers of conjugated diene hydrocarbons - C08L 23/0807: with unsaturated hydrocarbons only containing four or more carbon atoms - C08L 23/10: Homopolymers or copolymers of propene - C08L 23/12: Polypropene - C08L 23/142: {at least partially crystalline copolymers of propene with other olefins} - C08L: COMPOSITIONS OF MACROMOLECULAR COMPOUNDS (compositions based on polymerisable monomers C08F, C08G; artificial filaments or fibres D01F; textile treating compositions D06) ## Abstract The present invention relates to a polymer composition, comprising: (i) a polypropylene matrix; (ii) a first elastomeric phase dispersed within the matrix and having a glass transition temperature Tg1, measured with dynamical mechanical thermal analysis according to ISO 6721-2, wherein the first elastomeric phase comprises an ethylene copolymer having comonomer units derived from C3 to C8 olefins; (iii) a second elastomeric phase dispersed within the matrix, wherein the second elastomeric phase is crosslinked and has a glass transition temperature Tg2, measured with dynamical mechanical thermal analysis according to ISO 6721-2, within the range of −70° C. to −90° C., wherein the difference between Tg1 and Tg2 is at least 15° C. and Tg1 is higher than Tg2. ## Claims ### Claim 1 A polymer composition, comprising (i) a polypropylene matrix, wherein the polypropylene matrix is present in an amount of at least 60 wt %, based on the weight of the polymer composition, and said polypropylene matrix has a melt flow rate (MFR) of 10-30 g/10 min and a molecular weight distribution (MWD) of 5-8, (ii) a first elestomeric phase dispersed within the matrix and having a glass transition temperature Tg1, measured with dynamical mechanical thermal analysis according to ISO 6721-2, within the range of −58° C. to −64° C. wherein the first elastomeric phase comprises an ethylene copolymer having comonomer units derived from C3 to C8 olefins, wherein the intrinsic viscosity of the first elastomeric phase is 1 to 3.5 dl/g to provide high impact strength at low temperature, wherein the first elastomeric phase is non-crosslinked, wherein the first elastomeric phase is present in an amount of 10 to 30 wt % based on the weight of the polymer composition, (iii) a second elastomeric phase dispersed within the matrix, wherein the second elestomeric phase is crosslinked polybutadiene, and has a glass transition temperature Tg2, measured with dynamical mechanical thermal analysis according to ISO 6721-2, within the range of −75° C. to −85° C., wherein the second elastomeric phase is present in the form of discrete particles having a mean particle size from 250 to 500 nm, wherein the second elestomeric phase is present in an amount of 10 to 17 wt % based on the weight of the polymer composition, wherein the difference between Tg1 and Tg2 is at least 20° C. to 25° C. ### Claim 2 (depends on 1) The polymer composition according to claim 1, wherein the ethylene copolymer is an ethylene/propylene copolymer. ### Claim 3 (depends on 2) The polymer composition according to claim 2, wherein the ethylene/propylene copolymer has an amount of propylene units in the range of 25 to 75 wt %, based on the weight of the ethylene/propylene copolymer. ### Claim 4 (depends on 1) The polymer composition according to claim 1, wherein the ethylene copolymer has comonomer units derived from 1-butene, 1-hexene, 1-octene, or any mixture thereof. ### Claim 5 (depends on 4) The polymer composition according to claim 4, wherein the ethylene copolymer has an amount of comonomer units within the range of 5 to 50 wt %, based on the weight of the ethylene copolymer. ### Claim 6 (depends on 1) The polymer composition according to claim 1, wherein the polypropylene constituting the matrix is selected from the group consisting of propylene homopolymer, and a propylene copolymer having comonomer units derived from ethylene and/or C4 to C20. ### Claim 7 (depends on 6) The polymer composition according to claim 6, wherein the propylene homo- or copolymer constituting the matrix is present in an amount of at least 80 wt %, based on the weight of the polymer composition. ### Claim 8 A process for the preparation of a polymer composition comprising (i) providing a polypropylene matrix, wherein the polypropylene constituting the matrix is selected from the group consisting of a propylene homopolymer, a propylene copolymer having comonomer units derived from ethylene and/or C4 to C20 olefins, and any mixture thereof, wherein the polypropylene matrix is present in an amount of at least 60 wt %, based on the weight of the polymer composition; and said polypropylene matrix has a melt flow rate (MFR) of 10-30 g/10 min and a molecular weight distribution (MWD) of 5-8, (ii)providing a first elastomeric phase for disparing within the matrix and having glass transition temperature Tg1, measured with dynamical mechanical thermal analysis according to ISO 6721-2, within the range of −58° C. to −64° C., wherein the first elastomeric phase comprises an ethylene copolymer having comonomer units derived from C3 to C8 olefins, wherein the first elastomeric phase is non-crosslinked, wherein the first elastomeric phase is present in an amount of 10 to 30 wt %, based on the weight of the polymer composition; (iii)providing a second phase for dispersing within the matrix, wherein the second elastomeric phase is crosslinked polybutadiene and has a glass transition temperature Tg2, measured with dynamical mechanical thermal analysis according to ISO 6721-2, within the range of −75° C. to −85° C., wherein the second elastomeric phase, is present in the form of discrete particles having a mean particle size from 250 to 500 nm, wherein the second elastomeric phase is present in an amount of 10 to 17 wt %, based on the weight of the polymer composition, whereiin the differnce between Tg1 and Tg2 is at least 20° C. to 25° C., dispersing the first and the second elastomeric phases within the propylene homo- or copolymer constituting the matrix, wherein the first elastomeric phase is prepared separately, followed by the dispersion within the propylene homo- or copolymer constituting the matrix. ### Claim 9 (depends on 8) The process according to claim 8, wherein the second elastomeric phase is crosslinked prior to dispersion and subsequently dispersed within the propylene homo- or copolymer constituting the matrix. ### Claim 10 A process for the preparation of polymer composition comprising (i) providing a polypropylene matrix, wherein the polypropylene constituting the matrix is selected from the group consisting of a propylene homopolymer, a propylene copolymer having comonomer units derived from ethylene and/or C4 to C20 olefins, and any mixture thereof, wherein the polypropylene matrix is present in an amount of at least 60 wt %, based on the weight of the polymer composition; and said polypropylene matrix has a melt flow rate (MFR) of 10-30 g/10 min and a molecular weight distribution (MWD) of 5-8, (ii) providing a first elastomeric phase for dispersing within the matrix and having glass transition temperature Tg1, measured with dynamical mechanical thermal analysis according to ISO 6721-2, within the range of −58° C. to −64° C., wherein the first elestomeric phase comprises an ethylene copolymer having copolymer units derived from C3 to C8 olefins, wherein the first elastomeric phase is non-crosslinked, wherein the first elastomeric is present in an amount 10 to 30 wt %, based on the weight of the polymer composition, wherein the first elastomeric phase is in situ dispersed within the propylene homo- or copolymer constituting the matrix by reactor blending; (iii) providing a second elestomeric phase for dispersing within the matrix, wherein the second elastomeric phase is crosslinked polybutadiene and had a glass transition temperature Tg2, measured with dynamical mechanical thermal analysis according to ISO 6721-2, within the range of −75° C. to −85° C., wherein the second elastomeric phase is present in form of discrete particles having a mean particle ratze from 250 to 500 nm, wherein the second elastomeric phase is present in an amount of 10 to 17 based on the weight of the polymer composition, (iv) dispersing the second elastomeric phase within the propylene homo or copolymer constituting the matrix, wherein the difference between Tg1 and Tg2 is at least 20° C. to to 25° C. ### Claim 11 A shaped article, comprising a polymer composition comprising (i) a polypropylene matrix, wherein the polypropylene matrix is present in an amount of at least 60 wt %, based on the weight of the polymer composition; and said polypropylene matrix has a melt flow rate (MFR) of 10-30 g/10 min and a molecular weight distribution (MWD) of 5-8, (ii) a first elastomeric phase dispersed within the matrix and having a glass transition temperature Tg1, measured with dynamical mechanical thermal analysis according to ISO 6721-2, within the range of −58° C. to −64° C., wherein the first elastomeric phase comprises an ethylene copolymer having comonomer units derived from C3 to C8 olefins, wherein the first elastomeric phase is non-crosslinked, wherein the first elastomeric phase is present in an amount of 10 to 30 wt %, based on the weight of the polymer composition, wherein the intrinsic viscosity of the first elastomeric phase is 1 to 3.5 dl/g to provide high impact strength at low temperature, (iii) a second elastomeric phase dispersed within the matrix, wherein the second elastomeric phase is crosslinked polybutadiene and has a glass transition temperature Tg2, measured with dynamical mechanical thermal analysis according to ISO 6721-2, within the range of −75° C. to −85° C., wherein the second elastomeric phase is present in the form of discrete particles having a mean particle size from 250 to 500 nm, wherein the second elastomeric phase is present in an amount of 10 to 17 wt %, based on the weight of the polymer composition, wherein the differnce between the Tg1 and Tg2 is at least 20° C. to 25° C. ### Claim 12 (depends on 1) A shaped polymer article made from the composition according to claim 1, wherein shaped polymer article is a part for an interior or exterior automotive application.