Heterophasic propylene copolymer with low extractables
US-2017145199-A1 · May 25, 2017 · US
US9932469B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9932469-B2 |
| Application number | US-201515109855-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 6, 2015 |
| Priority date | Jan 7, 2014 |
| Publication date | Apr 3, 2018 |
| Grant date | Apr 3, 2018 |
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A heterophasic propylene ethylene copolymer having an MFR 2 of 0.5 to 100 g/10 m in and obtained using single site catalysis comprising: (i) a propylene homopolymer or propylene ethylene copolymer matrix having up to 4 wt % ethylene; and (ii) an ethylene propylene rubber (EPR) dispersed in the matrix; said heterophasic propylene ethylene copolymer having a xylene cold soluble content (XS) of 20 to 40%; wherein the ethylene content of the xylene cold soluble fraction of said heterophasic propylene ethylene copolymer is between 70 and 90 wt. %; wherein the xylene cold soluble fraction of said heterophasic propylene ethylene copolymer has an intrinsic viscosity (IV) of 3.0 dl/g or more; and wherein the melting enthalpy (ΔHM) of the heterophasic propylene ethylene copolymer is between 10 and 30 J/g at a temperature of 0 to 130° C.
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The invention claimed is: 1. A heterophasic propylene ethylene copolymer having an MFR 2 of 0.5 to 100 g/10 min and obtained using single site catalysis comprising: (i) a propylene homopolymer or propylene ethylene copolymer matrix having up to 4 wt % ethylene; and (ii) an ethylene propylene rubber (EPR) dispersed in the matrix; said heterophasic propylene ethylene copolymer having a xylene cold soluble content (XS) of 20 to 40%; wherein the ethylene content of the xylene cold soluble fraction of said heterophasic propylene ethylene copolymer is between 70 and 90 wt. %; wherein the xylene cold soluble fraction of said heterophasic propylene ethylene copolymer has an intrinsic viscosity (IV) of 3.0 dl/g or more; and wherein the melting enthalpy (ΔHm) of the heterophasic propylene ethylene copolymer is between 10 and 30 J/g at a temperature of 0 to 130° C. 2. A heterophasic copolymer as claimed in claim 1 which is formed in three steps. 3. A heterophasic copolymer as claimed in claim 1 wherein the matrix component is a homopolymer. 4. A heterophasic copolymer as claimed in claim 1 wherein there is 20 to 35 wt % XS component. 5. A heterophasic copolymer as claimed in claim 1 having an MFR 2 of 0.7 to 60 g/10 min. 6. A heterophasic copolymer as claimed in claim 1 wherein the C2(XS) content is 71 to 90 wt %. 7. A heterophasic copolymer as claimed in claim 1 wherein the IV(XS) is in the range of 3.0 to 4.0 dl/g. 8. A heterophasic copolymer as claimed in claim 1 wherein the charpy impact strength is at least 50 kJ/m 2 at 23° C. 9. A heterophasic copolymer as claimed in claim 1 wherein the brittle to ductile transition temperature occurs at 0° C. or less. 10. A heterophasic copolymer as claimed in claim 1 having at least two melting points. 11. A heterophasic copolymer as claimed in claim 1 wherein the glass transition temperature of the xylene soluble fraction is −30 to −45° C. 12. A process for the preparation of a heterophasic propylene ethylene copolymer as claimed in claim 1 comprising polymerising: (I) propylene and optionally ethylene so as to form a propylene homopolymer or propylene ethylene copolymer matrix having up to 4 wt % ethylene as said matrix component; and subsequently polymerising (II) propylene and ethylene so as to form an ethylene propylene rubber dispersed in the matrix; wherein both steps (I) and (II) take place in the presence of the same single site solid particulate catalyst free from an external carrier comprising (i) a complex of formula (I): wherein M is zirconium or hafnium; each X is a sigma ligand; L is a divalent bridge selected from —R′ 2 C—, —R′ 2 C—CR′ 2 —, —R′ 2 Si—, —R′ 2 Si—SiR′ 2 —, —R′ 2 Ge—, wherein each R′ is independently a hydrogen atom, C 1 -C 20 -hydrocarbyl, tri(C 1 -C 20 -alkyl)silyl, C 6 -C 20 -aryl, C 7 -C 20 -arylalkyl or C 7 -C 20 -alkylaryl; R 2 and R 2 ′ are each independently a C 1 -C 20 hydrocarbyl radical optionally containing one or more heteroatoms from groups 14-16; R 5′ is a C 1-20 hydrocarbyl group containing one or more heteroatoms from groups 14-16 optionally substituted by one or more halo atoms; R 6 and R 6′ are each independently hydrogen or a C 1-20 hydrocarbyl group optionally containing one or more heteroatoms from groups 14-16; R 7 and R 7′ are each independently hydrogen or C 1-20 hydrocarbyl group optionally containing one or more heteroatoms from groups 14-16; Ar is independently an aryl or heteroaryl group having up to 20 carbon atoms optionally substituted by one or more groups R 1 ; Ar′ is independently an aryl or heteroaryl group having up to 20 carbon atoms optionally substituted by one or more groups R 1 ; each R 1 is a C 1-20 hydrocarbyl group or two R 1 groups on adjacent carbon atoms taken together can form a fused 5 or 6 membered non aromatic ring with the Ar group, said ring being itself optionally substituted with one or more groups R 4 ; each R 4 is a C 1-20 hydrocarbyl group; and (ii) a cocatalyst comprising a compound of a group 13 metal. 13. A process for the preparation of a propylene ethylene copolymer as claimed in claim 12 in which the catalyst is prepared by obtaining a complex of formula (I) and a cocatalyst (ii); forming a liquid/liquid emulsion system, which comprises a solution of catalyst components (i) and (ii) dispersed in a solvent, and solidifying said dispersed droplets to form solid particles. 14. An article comprising the heterophasic propylene ethylene copolymer as claimed in claim 1 . 15. The process of claim 12 , wherein in step (II) propylene and ethylene are polymerised in the gas phase. 16. The process of claim 12 , wherein the group 13 metal is an aluminium compound or a boron compound. 17. The article of claim 14 , wherein the article comprises a film.
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