WO2009129873A1 - High purity heterophasic propylene copolymers - Google Patents
High purity heterophasic propylene copolymers Download PDFInfo
- Publication number
- WO2009129873A1 WO2009129873A1 PCT/EP2008/067858 EP2008067858W WO2009129873A1 WO 2009129873 A1 WO2009129873 A1 WO 2009129873A1 EP 2008067858 W EP2008067858 W EP 2008067858W WO 2009129873 A1 WO2009129873 A1 WO 2009129873A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- propylene
- copolymer
- catalyst system
- heterophasic polypropylene
- ethylene
- Prior art date
Links
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 title claims abstract description 62
- 229920001577 copolymer Polymers 0.000 title claims abstract description 38
- 239000003054 catalyst Substances 0.000 claims abstract description 47
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims abstract description 37
- 239000011159 matrix material Substances 0.000 claims abstract description 33
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 27
- 229920005606 polypropylene copolymer Polymers 0.000 claims abstract description 25
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 21
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000005977 Ethylene Substances 0.000 claims abstract description 20
- 229920001198 elastomeric copolymer Polymers 0.000 claims abstract description 20
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 16
- 238000004519 manufacturing process Methods 0.000 claims abstract description 15
- 239000004711 α-olefin Substances 0.000 claims abstract description 14
- 150000002430 hydrocarbons Chemical group 0.000 claims abstract description 12
- 238000005809 transesterification reaction Methods 0.000 claims abstract description 12
- 150000002148 esters Chemical class 0.000 claims abstract description 8
- 125000002524 organometallic group Chemical group 0.000 claims abstract description 7
- 238000000034 method Methods 0.000 claims description 40
- 229920000642 polymer Polymers 0.000 claims description 37
- 239000000203 mixture Substances 0.000 claims description 22
- 239000002002 slurry Substances 0.000 claims description 22
- 229920005989 resin Polymers 0.000 claims description 16
- 239000011347 resin Substances 0.000 claims description 16
- -1 polypropylene Polymers 0.000 claims description 12
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 claims description 11
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 claims description 9
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 claims description 9
- 229920001384 propylene homopolymer Polymers 0.000 claims description 8
- 239000004743 Polypropylene Substances 0.000 claims description 7
- 229920001155 polypropylene Polymers 0.000 claims description 7
- AIXMJTYHQHQJLU-UHFFFAOYSA-N chembl210858 Chemical compound O1C(CC(=O)OC)CC(C=2C=CC(O)=CC=2)=N1 AIXMJTYHQHQJLU-UHFFFAOYSA-N 0.000 claims description 5
- 229920005635 heterophasic propylene copolymer resin Polymers 0.000 claims description 5
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 claims description 4
- 239000000839 emulsion Substances 0.000 claims description 4
- 239000007921 spray Substances 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- KOFGHHIZTRGVAF-UHFFFAOYSA-N n-ethyl-n-triethoxysilylethanamine Chemical compound CCO[Si](OCC)(OCC)N(CC)CC KOFGHHIZTRGVAF-UHFFFAOYSA-N 0.000 claims description 3
- 125000005234 alkyl aluminium group Chemical group 0.000 claims description 2
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 claims description 2
- 238000012545 processing Methods 0.000 claims description 2
- 238000005406 washing Methods 0.000 claims description 2
- 239000012071 phase Substances 0.000 description 30
- 239000007789 gas Substances 0.000 description 26
- 239000000047 product Substances 0.000 description 16
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 10
- 239000010936 titanium Substances 0.000 description 10
- 229910052719 titanium Inorganic materials 0.000 description 10
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 9
- 239000003039 volatile agent Substances 0.000 description 9
- 239000012855 volatile organic compound Substances 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 7
- 238000004806 packaging method and process Methods 0.000 description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 6
- 239000000654 additive Substances 0.000 description 6
- 238000004458 analytical method Methods 0.000 description 6
- 238000013329 compounding Methods 0.000 description 6
- 238000009826 distribution Methods 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 230000002902 bimodal effect Effects 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 239000000155 melt Substances 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 239000002861 polymer material Substances 0.000 description 5
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 4
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 4
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 4
- 239000003963 antioxidant agent Substances 0.000 description 4
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 238000001746 injection moulding Methods 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 239000008188 pellet Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000000454 talc Substances 0.000 description 4
- 229910052623 talc Inorganic materials 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 150000001336 alkenes Chemical class 0.000 description 3
- 230000003078 antioxidant effect Effects 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 239000010408 film Substances 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- 239000008096 xylene Substances 0.000 description 3
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N 1-Heptene Chemical compound CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 2
- BJQHLKABXJIVAM-BGYRXZFFSA-N 1-o-[(2r)-2-ethylhexyl] 2-o-[(2s)-2-ethylhexyl] benzene-1,2-dicarboxylate Chemical compound CCCC[C@H](CC)COC(=O)C1=CC=CC=C1C(=O)OC[C@H](CC)CCCC BJQHLKABXJIVAM-BGYRXZFFSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- ZVFDTKUVRCTHQE-UHFFFAOYSA-N Diisodecyl phthalate Chemical compound CC(C)CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC(C)C ZVFDTKUVRCTHQE-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 2
- 238000005253 cladding Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 description 2
- JWCYDYZLEAQGJJ-UHFFFAOYSA-N dicyclopentyl(dimethoxy)silane Chemical compound C1CCCC1[Si](OC)(OC)C1CCCC1 JWCYDYZLEAQGJJ-UHFFFAOYSA-N 0.000 description 2
- YCZJVRCZIPDYHH-UHFFFAOYSA-N ditridecyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCCCCCC YCZJVRCZIPDYHH-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000012632 extractable Substances 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 230000014509 gene expression Effects 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 239000001307 helium Substances 0.000 description 2
- 229910052734 helium Inorganic materials 0.000 description 2
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 2
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 229910001701 hydrotalcite Inorganic materials 0.000 description 2
- 229960001545 hydrotalcite Drugs 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 150000002681 magnesium compounds Chemical class 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 239000002667 nucleating agent Substances 0.000 description 2
- FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 description 2
- 150000002902 organometallic compounds Chemical class 0.000 description 2
- 150000003961 organosilicon compounds Chemical class 0.000 description 2
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
- 230000000379 polymerizing effect Effects 0.000 description 2
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 2
- 229960003885 sodium benzoate Drugs 0.000 description 2
- 235000010234 sodium benzoate Nutrition 0.000 description 2
- 239000004299 sodium benzoate Substances 0.000 description 2
- 239000011949 solid catalyst Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- SDZIMLUTKIRUKC-UHFFFAOYSA-N 3-hexyl-4-propylphthalic acid Chemical compound CCCCCCC1=C(CCC)C=CC(C(O)=O)=C1C(O)=O SDZIMLUTKIRUKC-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- IJFPVINAQGWBRJ-UHFFFAOYSA-N Diisooctyl phthalate Chemical compound CC(C)CCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCC(C)C IJFPVINAQGWBRJ-UHFFFAOYSA-N 0.000 description 1
- 239000004150 EU approved colour Substances 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- 239000004609 Impact Modifier Substances 0.000 description 1
- 239000004594 Masterbatch (MB) Substances 0.000 description 1
- 239000012963 UV stabilizer Substances 0.000 description 1
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 229940078456 calcium stearate Drugs 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000012159 carrier gas Substances 0.000 description 1
- 239000012986 chain transfer agent Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000001647 drug administration Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000002737 fuel gas Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000007731 hot pressing Methods 0.000 description 1
- PQPVPZTVJLXQAS-UHFFFAOYSA-N hydroxy-methyl-phenylsilicon Chemical class C[Si](O)C1=CC=CC=C1 PQPVPZTVJLXQAS-UHFFFAOYSA-N 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 239000012764 mineral filler Substances 0.000 description 1
- 238000002392 multiple headspace extraction Methods 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- FATBGEAMYMYZAF-UHFFFAOYSA-N oleicacidamide-heptaglycolether Natural products CCCCCCCCC=CCCCCCCCC(N)=O FATBGEAMYMYZAF-UHFFFAOYSA-N 0.000 description 1
- 229940006093 opthalmologic coloring agent diagnostic Drugs 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920005629 polypropylene homopolymer Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000012763 reinforcing filler Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000012748 slip agent Substances 0.000 description 1
- 238000007669 thermal treatment Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000009849 vacuum degassing Methods 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/04—Monomers containing three or four carbon atoms
- C08F210/06—Propene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/10—Homopolymers or copolymers of propene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/10—Homopolymers or copolymers of propene
- C08L23/12—Polypropene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/16—Copolymers of ethene with alpha-alkenes, e.g. EP rubbers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2207/00—Properties characterising the ingredient of the composition
- C08L2207/02—Heterophasic composition
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/16—Elastomeric ethene-propene or ethene-propene-diene copolymers, e.g. EPR and EPDM rubbers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Definitions
- the present invention relates to heterophasic polypropylene copolymers with high purity, which is shown in reduced volatiles content, reduced fogging and a reduced hexane-solubles content. Furthermore, the present invention relates to a process for the production of such copolymers as well as to their use.
- Heterophasic propylene copolymers are well established in a lot of applications, such as moulding applications, films, wires and cables or pipes, because of their good stiffness/impact ratio together with good flowability.
- heterophasic polymers are used for the production of car exteriors and interiors, in particular dashboards, door claddings, consoles, trims and the like as well as in the packaging area for food and medicals.
- Heterophasic polymers are polymers having a matrix phase and a disperse phase.
- the matrix phase is usually a propylene homopolymer or copolymer phase and the disperse phase is often a propylene copolymer comprising ethylene and/or other higher ⁇ -olefin(s).
- Their preparation using different catalyst systems has been described in several patents and patent applications.
- EP 1 538 167 describes a method for polymerizing an olefin using a catalyst system which comprises the following components (A), (B) and (C):
- Component (A) a solid component (i) containing magnesium, titanium, halogen and an internal donor,
- Component (B) an organometallic compound and Component (C): an organosilicon compound represented by the formula Si(OR 1 ) 3 (NR 2 R 3 ) wherein R 1 is a hydrocarbon group having 1 to 6 carbon atoms, R 2 is a hydrocarbon group having 1 to 12 carbon atoms or hydrogen atom, and R 3 is a hydrocarbon group having 1 to 12 carbon atoms.
- Component (A) may be prepared for example by co-grinding a magnesium compound, an electron donor and a titanium halide compound, or by dispersing and dissolving them in a solvent to allow them to contact each other.
- a further method mentioned comprises dissolving a magnesium compound and an electron donor in a solvent and adding a titanium halide compound to the resulting solution to precipitate a solid catalyst.
- this catalyst system allows production of an alpha-olefin polymer, like heterophasic polypropylene copolymers, with high hydrogen response, high polymerization rate, high stereoregularity and good melt fluidity.
- the polymers produced can provide excellent performance to automobile and household electric structural materials.
- EP 1 783 145 discloses a method for polymerizing an olefin using a catalyst system which comprises the following components (A), (B) and (C):
- Component (A) a prepolymer obtained by olefin prepolymerisation on solid titanium catalyst component (A ' ), prepared by contacting a solid component (i) containing magnesium, titanium, halogen and an donor (c 3 ) , a polar compound (ii) having a dipole moment of 0.5 to 4.0 Debye, and at least one compound (iii) selected from liquid titanium (d) and an electron donor (e)
- Component (B) an organometallic compound and Component (C): an organosilicon compound represented by the formula Si(OR 1 ) 3 (NR 2 R 3 ) wherein R 1 is a hydrocarbon group having 1 to 8 carbon atoms, R 2 is a hydrocarbon group having 1 to 12 carbon atoms or hydrogen atom, and R 3 is a hydrocarbon group having 1 to 12 carbon atoms.
- the propylene copolymer compositions for example heterophasic polypropylene copolymer, obtained according to EP 1 783 145 can be processed into a desired moulded article such as for automotives.
- the only advantage mentioned in EP 1 783 145 is that olefinic polymers having high fluidity as well as high stereoregularity even without excessive use of hydrogen molecule as chain transfer agent can be effectively manufactured. No further advantageous properties of the obtained polymer compositions are mentioned.
- the disadvantage of this catalyst system is especially the complex preparation of the solid titanium catalyst component (A ' ).
- MFR melt flow rates
- LMW low molecular weight
- the LMW tail of the polymer composition comprises i.a. oligomers.
- the oligomers thus belong to a generally known group of compounds, namely volatiles. Such volatiles contribute also to the so called "fogging" problem, i.e. these compounds tend to separate, e.g. evaporate, from the polymer material and cause fogging on the surrounding surfaces e.g. on car windows. Therefore polymers with high MFR, but still low oligomer content are becoming increasingly important.
- polypropylene having a high MFR (>50 g/10 min), respectively low molecular weight, is an intrinsically very brittle material.
- MFR >50 g/10 min
- impact modifier high amounts of impact modifier. This in turn has an adverse effect on flow, stiffness and hexane extractables (hexane-solubles).
- VOC volatile organic compounds
- fogging In automotive applications, for example, key issues are low emissions as well as low amounts of volatile organic compounds (VOC) and fogging. Those VOCs are supposed to be produced during the extrusion or compounding step. Reducing emissions from the polymeric material applied in automobile interior is a general target for several years. This target has been pursued until now by applying purification steps in the production of the respective polymeric material (e.g. steam stripping, vacuum degassing and low input compounding) or by using special additives (e.g. high performance stabilizers and absorbers). Examples for such processes are disclosed in EP 1 364 760 A1 and EP 1 535 718 A1. These processes involve, however, increased investment cost and reduced output rates, deteriorating the economic situation of the resulting products.
- purification steps in the production of the respective polymeric material e.g. steam stripping, vacuum degassing and low input compounding
- special additives e.g. high performance stabilizers and absorbers
- heterophasic polypropylene copolymers which fulfil the increasing environmental and customer requirements in many end application areas of polymer materials, such as packaging, including food and medical packaging, fibre, pipe and automobile industry.
- These heterophasic polypropylene copolymers shall show desirable properties, such as improved high purity, respectively reduced volatiles content, reduced fogging and a reduced hexane-solubles content, while keeping the other properties needed for the production of moulded articles, like good stiffness/impact ratio together with good flowability. These properties shall be achieved without the need of any further treatment of the polymers for reducing the content of volatiles, hexane-solubles and fogging.
- the present invention resides in the finding that high purity heterophasic polypropylene copolymers are obtainable by a multi-step polymerization procedure in the presence of a special Ziegler-Natta procatalyst which contains a trans-esterification product of a lower alcohol and a phthalic ester in combination with a special external donor.
- the present invention is therefore directed to high purity heterophasic polypropylene copolymers comprising
- component (B) 2 to 27 wt% of an elastomeric copolymer, comprising propylene in an amount of at least 50 wt% of component (B) and at least ethylene and/or one other C 4 to Cio alpha olefin in an amount of up to 50 wt% of component (B), the heterophasic polypropylene copolymers being obtainable by a multistage polymerization process in the presence of a catalyst system comprising
- a Ziegler-Natta procatalyst which contains a trans-esterification product of a lower alcohol and a phthalic ester and (ii) optionally an organometallic cocatalyst and (iii) external donor represented by formula (I) Si(OCH 2 CHs) 3 (NR 1 R 2 ) wherein R 1 and R 2 can be the same or different a represent a hydrocarbon group having 1 to 12 carbon atoms.
- heterophasic polypropylene copolymers show low levels of emissions and volatiles, which can be seen in low emission and low amounts of VOC and fogging of the granulated compounds and the injection moulded articles made from those compounds. At the same time the good impact properties especially at low temperatures are achieved whereas the flexural properties are not affected. In addition the heterophasic polypropylene copolymers show low levels of hexane-solubles.
- the propylene matrix (A) can be a propylene homopolymer, a propylene copolymer or mixtures thereof, like a homo/random copolymer. However it is preferred that the propylene matrix (A) is a propylene homopolymer.
- the propylene matrix (A) is a propylene homopolymer
- the matrix may consist of a single propylene homopolymer, but may also comprise a mixture of different propylene homopolymers.
- the expression homopolymer used in the instant invention relates to a polypropylene that consists substantially, i.e. of at least 97 wt%, preferably of at least 98 wt%, more preferably of at least 99 wt%, still more preferably of at least 99,8 wt% of propylene units. In a preferred embodiment only propylene units in the propylene homopolymer are detectable.
- the comonomer content can be determined with FT infrared spectroscopy, as described below in the examples.
- the propylene matrix (A) comprises a propylene copolymer or is a homo/random propylene copolymer
- the propylene copolymer comprises monomers copolymerizable with propylene, for example comonomers such as ethylene and C 4 to C 2 0 alpha-olefins, in particular ethylene and C 4 to C 1 0 alpha-olefins, e.g. 1-butene or 1-hexene.
- the comonomer content in the propylene matrix is in such a case preferably relatively low, i.e. up to 6,0 wt%, more preferably 1 ,0 to 6,0 wt%, still more preferably 1 ,0 to 4,0 wt%, yet more preferably 1 ,0 to 3,0 wt%.
- the propylene matrix (A) can be unimodal or multimodal, like bimodal. However it is preferred that the propylene matrix (A) is unimodal. Concerning the definition of unimodal and multimodal, like bimodal, it is referred to the definition below.
- the matrix When the matrix is unimodal with respect to the molecular weight distribution, it may be prepared in a single stage process e.g. as slurry or gas phase process in a slurry or gas phase reactor. Preferably, the unimodal matrix is polymerized as a slurry polymerization. Alternatively, the unimodal matrix may be produced in a multistage process using at each stage process conditions which result in similar polymer properties.
- the propylene matrix (A) comprises two or more different propylene polymers these may be polymers with different monomer make up and/or with different molecular weight distributions. These components may have identical or differing monomer compositions and tacticities. Moreover it is preferred that the polymer matrix (A) has a rather high melt flow rate (MFR), i.e. a rather low molecular weight.
- MFR melt flow rate
- the melt flow rate measured under a load of 2,16 kg at 230 0 C (ISO 1 133) is denoted as MFR 2 (230 0 C). Accordingly, it is preferred that in the present invention the propylene matrix (A) has an MFR 2 (230 0 C) equal to or above 45 g/10 min. Preferably the propylene matrix (A) has an MFR 2 (230°C) equal to or above 50 g/10 min, more preferably equal to or above 55 g/10 min. The MFR 2 (230°C) can be up to 500 g/10 min.
- the elastomeric copolymer must fulfill some properties so that the desired results can be achieved.
- the elastomeric copolymer (B) must comprise propylene and at least ethylene and/or one other C 4 to Cio alpha-olefin.
- the elastomeric copolymer (B) comprises, preferably consists of, propylene and at least one alpha-olefin comonomer selected from the group consisting of ethylene, 1-butene, 1-pentene, 1-hexene, 1-heptene and 1-octene.
- the elastomeric copolymer (B) comprises at least propylene and ethylene and may comprise a further alpha-olefin as defined in this paragraph.
- the elastomeric copolymer (B) comprises, more preferably consists of, propylene and ethylene as the only polymerizable units.
- an ethylene-propylene rubber (EPR) as elastomeric copolymer (B) is most preferred.
- the elastomeric copolymer (B) can be unimodal or multimodal, like bimodal. However it is preferred that the elastomeric copolymer (B) is unimodal. Concerning the definition of unimodal and multimodal, like bimodal, it is referred to the definition below.
- the elastomeric copolymer (B) is in particular featured by an amount of other C 2 to Cio alpha-olefin than propylene lower than 50 wt%. Accordingly the amount of the other C 2 to Cio alpha-olefin(s), i.e. excluding propylene, in the elastomeric copolymer (B) is up to 50 wt%, more preferably up to 40 wt%. Preferred ranges for the other C 2 to Cio alpha-olefin(s), i.e. excluding propylene, in the elastomeric copolymer (B) is 20 to 50 wt%, preferably 20 to 40 wt%.
- the elastomeric copolymer (B) is an ethylene-propylene rubber (EPR), in particular with propylene and/or ethylene content as defined in this paragraph.
- EPR ethylene-propylene rubber
- heterophasic propylene copolymer comprises
- the MFR (230 0 C) of the heterophasic propylene copolymer is rather high, i.e. above 35 g/10 min, more preferably above 40 g/10 min.
- multimodal or “bimodal” or “unimodal” used herein refers to the modality of the polymer, i.e. the form of its molecular weight distribution curve, which is the graph of the molecular weight fraction as a function of its molecular weight.
- the polymer components of the present invention are produced in a sequential step process, using reactors in serial configuration and operating at different reaction conditions. As a consequence, each fraction prepared in a specific reactor will have its own molecular weight distribution. When the molecular weight distribution curves from these fractions are superimposed to obtain the molecular weight distribution of the final polymer, that curve may show two or more maxima or at least be distinctly broadened when compared with curves for the individual fractions.
- the heterophasic propylene copolymer discussed above is produced in a multistage process, wherein the propylene matrix (A) is produced at least in one slurry reactor and subsequently the elastomeric copolymer (B) is produced at least in one gas phase reactor.
- the polymerization system can comprise one or more conventional stirred slurry reactors and/or one or more gas phase reactors.
- the reactors used are selected from the group of loop and gas phase reactors and, in particular, the process employs at least one loop reactor and at least one gas phase reactor. It is also possible to use several reactors of each type, e.g. one loop and two or three gas phase reactors, or two loops and one or two gas phase reactors, in series.
- the process comprises also a prepolymerization with the chosen catalyst system, as described in detail below, comprising the special Ziegler-Natta procatalyst, the external donor and optionally the cocatalyst.
- the chosen catalyst system as described in detail below, comprising the special Ziegler-Natta procatalyst, the external donor and optionally the cocatalyst.
- the prepolymerisation is conducted as bulk slurry polymerisation in liquid propylene, i.e. the liquid phase mainly comprises propylene, with minor amount of other reactants and optionally inert components dissolved therein.
- the prepolymerisation reaction is typically conducted at a temperature of 0 to 50 0 C, preferably from 10 to 45 0 C, and more preferably from 15 to 40 0 C.
- the pressure in the prepolymerisation reactor is not critical but must be sufficiently high to maintain the reaction mixture in liquid phase. Thus, the pressure may be from 20 to 100 bar, for example 30 to 70 bar.
- the catalyst components are preferably all introduced to the prepolymerisation step.
- the solid catalyst component (i) and the cocatalyst (ii) can be fed separately it is possible that only a part of the cocatalyst is introduced into the prepolymerisation stage and the remaining part into subsequent polymerisation stages. Also in such cases it is necessary to introduce so much cocatalyst into the prepolymerisation stage that a sufficient polymerisation reaction is obtained therein.
- hydrogen may be added into the prepolymerisation stage to control the molecular weight of the prepolymer as is known in the art.
- antistatic additive may be used to prevent the particles from adhering to each other or to the walls of the reactor.
- a slurry reactor designates any reactor, such as a continuous or simple batch stirred tank reactor or loop reactor, operating in bulk or slurry and in which the polymer forms in particulate form.
- “Bulk” means a polymerization in reaction medium that comprises at least 60wt% monomer.
- the slurry reactor comprises a bulk loop reactor.
- Gas phase reactor means any mechanically mixed or fluid bed reactor.
- the gas phase reactor comprises a mechanically agitated fluid bed reactor with gas velocities of at least 0.2 m/sec.
- the particularly preferred embodiment of the invention comprises carrying out the polymerization in a process comprising either a combination of one loop and one or two gas phase reactors or a combination of two loops and one or two gas phase reactors.
- a preferred multistage process is a slurry-gas phase process, such as developed by Borealis and known as the Borstar ® technology.
- a slurry-gas phase process such as developed by Borealis and known as the Borstar ® technology.
- EP 0 887 379 A1 WO 92/12182, WO 2004/000899, WO 2004/11 1095, WO 99/24478, WO 99/24479 and WO 00/68315 incorporated herein by reference.
- a further suitable slurry-gas phase process is the Spheripol® process of Basell.
- heterophasic propylene copolymers with improved purity according to the invention are produced by using a special Ziegler-Natta procatalyst in combination with a special external donor, as described below in detail, in the Spheripol® or in the Borstar®PP process.
- One preferred multistage process may therefore comprise the steps of: producing a polypropylene polymer matrix (A) in the presence of the chosen catalyst system, as described in detail below, comprising the special Ziegler-Natta procatalyst (i), an external donor (iii) and optionally the cocatalyst (ii) in a first slurry reactor and optionally in a second slurry reactor, both slurry reactors using the same polymerization conditions,
- said 1 st and 2 nd ethylene/propylene mixtures may have the same or different composition ratios and recovering the polymer product for further processing.
- the reaction product of the slurry polymerization which preferably is carried out in a loop reactor, is then transferred to the subsequent gas phase reactor, wherein the temperature preferably is within the range of from 50°C to 130°C, more preferably 60°C to 100°C, at a pressure in the range of from 5 to 50 bar, preferably 8 to 35 bar, again with the option of adding hydrogen in order to control the molecular weight in a manner known per se.
- the residence time can vary in the reactor zones identified above.
- the residence time in the slurry reactor for example a loop reactor, is in the range of from 0.5 to 5 hours, for example 0.5 to 2 hours, while the residence time in the gas phase reactor generally will be from 1 to 8 hours.
- the polymerization may be effected in a known manner under supercritical conditions in the slurry, preferably loop reactor, and/or as a condensed mode in the gas phase reactor.
- the high purity heterophasic propylene copolymers are obtained by a multistage polymerization process, as described above, in the presence of a catalyst system comprising as component (i) a Ziegler-Natta procatalyst which contains a trans- esterification product of a lower alcohol and a phthalic ester.
- a catalyst system comprising as component (i) a Ziegler-Natta procatalyst which contains a trans- esterification product of a lower alcohol and a phthalic ester.
- the procatalyst used according to the invention is prepared by a) reacting a spray crystallized or emulsion solidified adduct of MgCI 2 and a CrC 2 alcohol with TiCI 4 b) reacting the product of stage a) with a dialkylphthalate of formula (I)
- R 1 and R 2 are independently at least a C 5 alkyl
- step c) washing the product of stage b) or d) optionally reacting the product of step c) with additional TiCI 4
- the procatalyst is produced as defined for example in the patent applications WO 87/07620, WO 92/19653, WO 92/19658 and EP 0 491 566.
- the content of these documents is herein included by reference.
- the adduct which is first melted and then spray crystallized or emulsion solidified, is used as catalyst carrier.
- dialkylphthalate of formula (I) with R 1 and R 2 being independently at least a C 5 -alkyl, like at least a C 8 -alkyl, or preferably (ii) a dialkylphthalate of formula (I) with R 1 and R 2 being the same and being at least a C 5 -alkyl, like at least a C 8 -alkyl or more preferably (iii) a dialkylphthalate of formula (I) selected from the group consisting of propylhexylphthalate (PrHP), dioctylphthalate (DOP), di-iso-decylphthalate (DIDP), and ditridecylphthalate (DTDP), yet more preferably the dialkylphthalate of formula (I) is a dioctylphthalate (DOP), like di-iso- octylphthalate or diethylhexylphthalate, in particular diethylhexylphthalate, to
- R 1 and R 2 being methyl or ethyl, preferably ethyl, the dialkylphthalat of formula (II) being the internal donor and
- the adduct of the formula MgCl 2 * nROH, wherein R is methyl or ethyl and n is 1 to 6, is in a preferred embodiment melted and then the melt is preferably injected by a gas into a cooled solvent or a cooled gas, whereby the adduct is crystallized into a morphologically advantageous form, as for example described in WO 87/07620.
- This crystallized adduct is preferably used as the catalyst carrier and reacted to the procatalyst useful in the present invention as described in WO 92/19658 and WO 92/19653.
- the transesterification is performed at a temperature above 100 0 C, advantageously between 130 to 150 0 C.
- the procatalyst used according to the invention contains 2.5% by weight of titanium at the most, preferably 2.2% by weight at the most and more preferably 2.0 % by weight at the most. Its donor content is preferably between 4 to 12% by weight and more preferably between 6 and 10 % by weight. More preferably the procatalyst used according to the invention has been produced by using ethanol as the alcohol and dioctylphthalate (DOP) as dialkylphthalate of formula (I), yielding diethyl phthalate (DEP) as the internal donor compound.
- DOP dioctylphthalate
- DEP diethyl phthalate
- the catalyst used according to the invention is the BC-1 catalyst of Borealis (prepared according to WO92/19653 as disclosed in WO 99/24479; especially with the use of dioctylphthalate as dialkylphthalate of formula (I) according to WO 92/19658) or the catalyst Polytrack 8502, commercially available from Grace.
- the Ziegler-Natta procatalyst can be modified by polymerising a vinyl compound in the presence of the catalyst system, comprising the special Ziegler-Natta procatalyst, an external donor and optionally a cocatalyst, which vinyl compound has the formula:
- Crl2 CH-CHR6R7 wherein R 6 and R 7 together form a 5- or 6-membered saturated, unsaturated or aromatic ring or independently represent an alkyl group comprising 1 to 4 carbon atoms, and the modified catalyst is used for the preparation of the polymer composition.
- the polymerised vinyl compound can act as a nucleating agent.
- the catalyst system used preferably comprises in addition to the special Ziegler- Natta procatalyst an organometallic cocatalyst as component (ii). Accordingly it is preferred to select the cocatalyst from the group consisting of trialkylaluminium, like triethylaluminium (TEA), dialkyl aluminium chloride and alkyl aluminium sesquichloride.
- TAA triethylaluminium
- dialkyl aluminium chloride dialkyl aluminium chloride
- alkyl aluminium sesquichloride alkyl aluminium sesquichloride
- Component (iii) of the catalysts system used is an external donor represented by formula (I)
- R 1 and R 2 can be the same or different a represent a hydrocarbon group having 1 to 12 carbon atoms.
- R 1 and R 2 are independently selected from the group consisting of linear aliphatic hydrocarbon group having 1 to 12 carbon atoms, branched aliphatic hydrocarbon group having 1 to 12 carbon atoms and cyclic aliphatic hydrocarbon group having 1 to 12 carbon atoms.
- R 1 and R 2 are independently selected from the group consisting of methyl, ethyl, n-propyl, n-butyl, octyl, decanyl, iso-propyl, iso-butyl, iso-pentyl, tert. -butyl, tert.-amyl, neopentyl, cyclopentyl, cyclohexyl, methylcyclopentyl and cycloheptyl. More preferably both R 1 and R 2 are the same, yet more preferably both R 1 and R 2 are an ethyl group. Most preferably diethylaminotriethoxysilane is used as external donor.
- the external donor may be produced according to the methods disclosed in EP 1538 167.
- the content of this document is herein included by reference.
- the invention therefore also is related to a new catalyst system comprising
- R 1 and R 2 can be the same or different a represent a hydrocarbon group having 1 to 12 carbon atoms, and the use of it for the production of high purity heterophasic polypropylene copolymers.
- the current invention also provides a multistage process for producing heterophasic propylene copolymers using the special catalyst system comprising components (i), (ii) and (iii).
- the copolymers of the invention may further contain various conventional additives, such as miscible thermoplastics, antioxidants, UV-stabilizers, acid scavengers, lubricants, demoulding agents, nucleating agents, fillers, colouring agents, etc. in an amount of 0.001 to 10 wt. %, preferably up to 5.0 wt% and more preferably up to 3.0 wt% based on the weight of the heterophasic propylene copolymer.
- various conventional additives such as miscible thermoplastics, antioxidants, UV-stabilizers, acid scavengers, lubricants, demoulding agents, nucleating agents, fillers, colouring agents, etc.
- Moulding resin formulations comprising the heterophasic propylene copolymers produced according to the invention may further comprise 0,3 to 40 wt% of one or more particulate of fibrous reinforcing fillers such as glass fiber or carbon fiber, graphite, carbon black or the like, or fillers such as clay, talc and mineral fillers and the like commonly employed in the trade for the manufacture of molded articles and extruded goods.
- fibrous reinforcing fillers such as glass fiber or carbon fiber, graphite, carbon black or the like, or fillers such as clay, talc and mineral fillers and the like commonly employed in the trade for the manufacture of molded articles and extruded goods.
- the additives are added to the heterophasic propylene copolymer, which is collected from the final reactor of the series of reactors.
- these additives are mixed into the composition prior to or during the extrusion process in a one-step compounding process.
- a master batch may be formulated, wherein the heterophasic propylene copolymer is first mixed with only some of the additives.
- a conventional compounding or blending apparatus e.g. a Banbury mixer, a 2- roll rubber mill, Buss-co-kneader or a twin screw extruder may be used.
- the polymer materials recovered from the extruder are usually in the form of pellets. These pellets are then preferably further processed, e.g. by injection moulding to generate articles and products of the inventive heterophasic propylene copolymers.
- Heterophasic propylene copolymers according to the invention may be pelletized and compounded using any of the variety of compounding and blending methods well known and commonly used in the resin compounding art.
- the compositions of the current invention are preferably used for the production of moulded articles, preferably injection moulded articles. Even more preferred is the use for the production of thin wall packaging articles, household electrical materials and automotive applications, especially of car interiors and exteriors, in particular car interiors as for example dashboards, door claddings, consoles, trims and the like and for food and medical packaging.
- the current invention also provides articles comprising the inventive high purity heterophasic propylene copolymers. Preferably, these articles are produced by injection moulding.
- the polymer compositions according to the invention show lower amount of volatiles, fogging, emission and hexane-solubles compared to other polymer compositions known from the state of the art.
- good impact properties such as Charpy notched impact strength, especially at low temperatures are achieved whereas the flexural and tensile properties in behalf of flexural and tensile modulus are not affected.
- the invention may also be characterized as a method for improving purity of heterophasic propylene copolymer resin articles, the method comprising providing an article moulded from a heterophasic propylene copolymer resin, produced in the presence of the above described special catalyst system comprising components (i), (ii) and (iii).
- melt flow rate was measured as the MFR 2 in accordance with ISO 1 133 (230 0 C, 2.16 kg load) for polypropylene and is indicated in g/10 min.
- MFR is an indication of the flowability, and hence the processability, of the polymer. The higher the melt flow rate, the lower the viscosity of the polymer.
- the tensile modulus was measured according to ISO 572-3 at 1 mm/min and 23°C. Test specimens as described in EN ISO 1873-2 (80 x 10 x 4 mm) were used.
- the xylene soluble fraction (XS) as defined and described in the present invention was determined as follows: 2.0 g of the polymer were dissolved in 250 mm p-xylene at 135 0 C under agitation. After 30 minutes, the solution was allowed to cool for 15 minutes at ambient temperature and then allowed to settle for 30 minutes at 25 ⁇ 0.5 0 C. The solution was filtered with filter paper into two 100 mm flasks. The solution from the first 100 mm vessel was evaporated in nitrogen flow and the residue dried under vacuum at 90 0 C until constant weight is reached. The xylene soluble fraction (percent) can then be determined as follows:
- the intrinsic viscosity (IV) value increases with the molecular weight of a polymer.
- the IV values e.g. of the amorphous phase were measured according to ISO 1628/1 (October 1999) in Decalin at 135°C.
- NIS was determined according to ISO 179-1 eA:2000 on V-notched samples of 80x10x4 mm 3 at 23 0 C (Charpy notched impact strength (23 0 C)), and -20 0 C (Charpy notched impact strength (-20 0 C)).
- the test specimens were prepared by injection moulding using a IM V 60 TECH machinery in line with ISO 1872-2. The melt temperature was 200 °C and the mold temperature was 40 0 C.
- IFWI was determined according to ISO 6603-2 with a velocity of 4.4 m/s on 60x60x2 mm 3 plates, prepared by injection moulding, at +23°C, 0 0 C and -20 0 C.
- the total emission of the polymers was determined by using multiple head space extraction according to VDA 277:1995 using a gas chromatograph and a headspace method.
- the equipment was a Hewlett Packard gas chromatograph with a WCOT-capillary column (wax type) of 30 m length and 0.25 mm x 2.5 ⁇ m inner diameter (0.25 ⁇ m film thickness).
- a flame ionisation detector was used with hydrogen as a fuel gas.
- the GC settings were as follows: 3 minutes isothermal at 50 °C, heat up to 200 0 C at 12 K/min, 4 minutes isothermal at 200 0 C, injection-temperature: 200 0 C, detection-temperature: 250 °C, carrier helium, flow-mode split 1 :20 and average carrier-speed 22 - 27 cm/s.
- the emission potential was measured on the basis of the sum of all values provided by the emitted substances after gas chromatography analysis and flame ionization detection with acetone as the calibration standard.
- Sample introduction (pellets, about 1 gram) was by headspace analysis (10 ml head space vial) after conditioning at 120°C for 5 hours prior to the measurement.
- the unit is ⁇ gC/g ( ⁇ g carbon per g of sample). j) VOC/FOG Emission
- VOC/FOG emission was measured according to VDA 278:2002 on the granulated compounds.
- the volatile organic compounds are measured in toluene equivalents per gram sample ( ⁇ gTE/g).
- the fogging is measured in hexadecane equivalents per gram sample ( ⁇ gHD/g).
- the measurements were carried out with a TDSA supplied by Gerstel using helium 5.0 as carrier gas and a column HP Ultra 2 of 50 m length and 0.32 mm diameter and 0.52 ⁇ m coating of 5 % Phenyl-Methyl-Siloxane.
- the VOC-Analysis was done according to device setting 1 listed in the standard using following main parameters: flow mode splitless, final temperature 90 0 C; final time 30 min, rate 60K/min.
- the cooling trap was purged with a flow-mode split 1 :30 in a temperature range from -150 0 C to + 280 0 C with a heating rate of 12 K/sec and a final time of 5 min.
- the following GC settings were used for analysis: 2 min isothermal at 40 0 C. heating at 3 K/min up to 92 0 C, then at 5 K/min up to 160 0 C, and then at 10 K/min up to 280 0 C, 10 minutes isothermal; flow 1 ,3 ml/min.
- the FOG analysis was done according to device setting 1 listed in the standard using following main parameters: flow-mode splitless, rate 60K/min; final temperature 120 0 C; final time 60 min.
- the cooling trap was purged with a flow-mode split 1 :30 in a temperature range from -150 0 C to + 280 0 C with a heating rate of 12 K/sec.
- the following GC-settings were used for analysis: isothermal at 50 0 C for 2 min, heating at 25 K/min up to 160 0 C, then at 10 K/min up to 280 0 C, 30 minutes isothermal; flow 1 ,3 ml/min.
- hexane-solubles The content of hexane-solubles was determined according to FDA CFR 21 ⁇ 177.1520. Procedure: 1 g sample of a polymer film of 100 ⁇ m thickness (produced on a PM30 cast film line using chill-roll temperature of 40 0 C) was extracted at 50 0 C in 400 ml n-hexane for 2 hours and then filtered on a filter paper N°41. The filtrate was then evaporated and the total residue weighed as a measure of the n-hexane extractable fraction.
- Fogging (mg) Fogging has been determined according to DIN75201 , Part B on 2 mm thick compression molded plaques. Thermal treatment was performed at 100 0 C for 16 hours. Fogging is expressed as a difference in weight before and after treatment.
- the Base resins were produced in a plant having a prepolymerization reactor, a loop reactor and one fluid bed gas-reactor connected in series.
- the catalyst used in the polymerization was prepared according to WO 92/19653 with DOP as dialkylphthalat of the formula (I) and ethanol as alcohol, the cocatalyst was Triethylaluminium (TEA) and as an external donor diethylamino triethoxy silane was used.
- the catalyst system was fed to the slurry reactor, where the polymerisation of the polypropylene homopolymer matrix phase was performed.
- the slurry phase loop reactor was then followed by a gas phase reactor in series, in which the elastomeric rubber disperse phase was produced by copolymerisation of propylene with ethylene comonomer.
- the Base resins 1-3 contained a unimodal matrix and a unimodal rubber.
- the Comparative resins 4 and 5 were produced in a plant having a prepolymerization reactor, one loop reactor and one gas phase reactor connected in series as described for Base resins 1-3.
- the catalyst used in the polymerization was the same as for Examples 1-3, the cocatalyst was Triethylaluminium (TEA) and as an external donor dicyclopentyl dimethoxy silane was used.
- TAA Triethylaluminium
- the Comparative resins 6-8 were produced in a plant having a prepolymerization reactor, one loop reactor and one gas phase reactor connected in series as described for Base resins 1-3.
- the catalyst used in the polymerization was the ZN1 18 catalyst commercially available from Basell, the cocatalyst was Triethylaluminium (TEA) and as an external donor dicyclopentyl dimethoxy silane was used. Reaction conditions:
- Base resins 1-8 were initially obtained in powder form.
- Base resins 1 , 4 and 6 were mixed with 0,1 [wt%] talc A3 (from Luzenac (Naintsch) ), 0,2 [wt%] SHT (synthetic hydrotalcite; DHT-4A from Kyowa), 0,15 [wt%] Irganox1010 (Ciba Speciality Chemicals, antioxidant), 0,1 [wt%] lrgafos 168 (Ciba Speciality Chemicals, stabilizer), 0,15 [wt%] OSA (oleamide (9-octadecenamide) from Croda Chemical, slip agent) and 0,08 [wt%] sodiumbenzoate.
- talc A3 from Luzenac (Naintsch)
- SHT synthetic hydrotalcite
- DHT-4A synthetic hydrotalcite
- Irganox1010 Ciba Speciality Chemicals, antioxidant
- lrgafos 168 Ciba Speciality Chemicals, stabilizer
- OSA oleamide (9-
- Base resins 2 and 7 were mixed with 0,5 [wt%] talc A3 (from Luzenac (Naintsch) ), 0,05 [wt%] calciumstearate and 0,1 [wt%] Irganox B215 (Ciba Speciality Chemicals, antioxidant).
- Base resins 3, 5 and 8 were mixed with 0,7 [wt%] talc A3 (from Luzenac (Naintsch) ), 0,2 [wt%] %] SHT (synthetic hydrotalcite; DHT-4A from Kyowa), 0,1 [wt%] sodiumbenzoate and 0,1 [wt%] Irganox B215 (Ciba Speciality Chemicals, antioxidant).
- the mixtures were compounded by feeding the components to a Prism 24twin-screw extruder (Prism Ltd., Staffordshire, UK). The material was then extruded through a strand die, cooled and chopped to form pellets.
- VOC [ ⁇ gTE/g] na na na 336 409 408 584 454
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Description
Claims
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT08873974T ATE551395T1 (en) | 2008-04-24 | 2008-12-18 | HIGHLY PURE HETEROPHASIC PROPYLENE COPOLYMERS |
RU2010143172/04A RU2470946C2 (en) | 2008-04-24 | 2008-12-18 | High-purity heterophase propylene copolymers |
EP08873974.3A EP2283072B2 (en) | 2008-04-24 | 2008-12-18 | Process for producing high purity heterophasic propylene copolymers |
BRPI0822601-6A BRPI0822601B1 (en) | 2008-04-24 | 2008-12-18 | copolymers of heterophasic polypropylene with high purity, its production process, and article |
CN2008801289613A CN102015879B (en) | 2008-04-24 | 2008-12-18 | High purity heterophasic propylene copolymers |
US12/736,586 US9255166B2 (en) | 2008-04-24 | 2008-12-18 | High purity heterophasic propylene copolymers |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP08103707.9 | 2008-04-24 | ||
EP08103707 | 2008-04-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2009129873A1 true WO2009129873A1 (en) | 2009-10-29 |
Family
ID=39764924
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2008/067858 WO2009129873A1 (en) | 2008-04-24 | 2008-12-18 | High purity heterophasic propylene copolymers |
Country Status (7)
Country | Link |
---|---|
US (1) | US9255166B2 (en) |
EP (1) | EP2283072B2 (en) |
CN (1) | CN102015879B (en) |
AT (1) | ATE551395T1 (en) |
BR (1) | BRPI0822601B1 (en) |
RU (1) | RU2470946C2 (en) |
WO (1) | WO2009129873A1 (en) |
Cited By (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2226337A1 (en) * | 2009-03-02 | 2010-09-08 | Borealis AG | Process for the production of polypropylene random copolymers for injection moulding applications |
WO2010149529A1 (en) * | 2009-06-22 | 2010-12-29 | Borealis Ag | Heterophasic polypropylene copolymer composition |
WO2010149546A1 (en) * | 2009-06-22 | 2010-12-29 | Borealis Ag | Stabilized polypropylene-talc composite |
EP2397517A1 (en) | 2010-06-16 | 2011-12-21 | Borealis AG | Propylene polymer compositions having superior hexane extractables/impact balance |
CN102432701A (en) * | 2010-09-29 | 2012-05-02 | 中国石油化工股份有限公司 | Catalyst for olefin polymerization |
EP2452975A1 (en) * | 2010-11-12 | 2012-05-16 | Borealis AG | Soft heterophasic propylene copolymers |
EP2452956A1 (en) * | 2010-11-12 | 2012-05-16 | Borealis AG | Improved process for polymerising propylene |
EP2452957A1 (en) | 2010-11-12 | 2012-05-16 | Borealis AG | Improved process for producing heterophasic propylene copolymers |
EP2492309A1 (en) | 2011-02-28 | 2012-08-29 | Borealis AG | Heterophasic polyolefin composition having improved flowability and impact strength |
EP2492310A1 (en) | 2011-02-28 | 2012-08-29 | Borealis AG | Heterophasic polyolefin composition having improved flowability and impact strength |
EP2666817A1 (en) * | 2012-05-24 | 2013-11-27 | Borealis AG | Soft heterophasic polyolefin composition having low C6 extractables |
EP3015503A1 (en) | 2014-10-27 | 2016-05-04 | Borealis AG | Heterophasic polypropylene with improved stiffness/impact balance |
WO2016198344A1 (en) | 2015-06-12 | 2016-12-15 | Sabic Global Technologies B.V. | Process for manufacture of low emission polypropylene |
WO2017148970A1 (en) | 2016-03-04 | 2017-09-08 | Borealis Ag | High flow heterophasic polyolefin composition having improved stiffness/impact balance |
EP3260489A1 (en) * | 2016-06-24 | 2017-12-27 | Borealis AG | Novel polypropylene compositions with low fogging |
EP3071607B1 (en) | 2013-11-22 | 2018-05-09 | Borealis AG | Low emission propylene homopolymer |
US10072139B2 (en) | 2012-09-19 | 2018-09-11 | Saudi Basic Industries Corporation | Process for the preparation of a composition comprising heterophasic propylene co-polymer and talc |
CN109153830A (en) * | 2016-06-28 | 2019-01-04 | 博里利斯股份公司 | Soft and transparent polypropene composition |
WO2019162932A1 (en) | 2018-02-20 | 2019-08-29 | Carmel Olefins Ltd. | Polypropylene impact copolymers with reduced emission of volatiles |
WO2021045889A1 (en) * | 2019-09-05 | 2021-03-11 | Exxonmobil Chemical Patents Inc. | Processes for producing polyolefins and impact copolymers with broad molecular weight distribution and high stiffness |
US11370904B2 (en) | 2017-06-29 | 2022-06-28 | Borealis Ag | Process for preparing a polypropylene composition |
US11441024B2 (en) | 2017-12-14 | 2022-09-13 | Borealis Ag | Process for preparing a polypropylene composition |
US11447623B2 (en) | 2017-06-29 | 2022-09-20 | Borealis Ag | Process for preparing a polypropylene composition |
Families Citing this family (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE602005012122D1 (en) * | 2005-11-16 | 2009-02-12 | Borealis Tech Oy | Polypropylene resin composition with low shrinkage, high impact resistance, stiffness and scratch resistance |
JP6050508B2 (en) * | 2012-10-11 | 2016-12-21 | アブ ダビ ポリマーズ シーオー.エルティーディー (ボルージュ) エルエルシー | Heterogeneous polypropylene composition |
EP2746295A1 (en) * | 2012-12-21 | 2014-06-25 | Borealis AG | Transparent thin wall packaging material with improved stiffness and flowability |
KR102100006B1 (en) * | 2013-02-27 | 2020-05-26 | 도호 티타늄 가부시키가이샤 | Method for producing propylene block copolymer |
EP2824142B1 (en) * | 2013-07-12 | 2016-04-13 | Borealis AG | Heterophasic copolymer |
ES2622299T3 (en) * | 2014-01-07 | 2017-07-06 | Borealis Ag | Heterophasic Polypropylene Polymer |
US10647795B2 (en) | 2014-02-07 | 2020-05-12 | Eastman Chemical Company | Adhesive composition comprising amorphous propylene-ethylene copolymer and polyolefins |
US10696765B2 (en) | 2014-02-07 | 2020-06-30 | Eastman Chemical Company | Adhesive composition comprising amorphous propylene-ethylene copolymer and propylene polymer |
US10308740B2 (en) | 2014-02-07 | 2019-06-04 | Eastman Chemical Company | Amorphous propylene-ethylene copolymers |
US9382351B2 (en) | 2014-02-07 | 2016-07-05 | Eastman Chemical Company | Amorphous propylene-ethylene copolymers |
US10723824B2 (en) | 2014-02-07 | 2020-07-28 | Eastman Chemical Company | Adhesives comprising amorphous propylene-ethylene copolymers |
US11267916B2 (en) | 2014-02-07 | 2022-03-08 | Eastman Chemical Company | Adhesive composition comprising amorphous propylene-ethylene copolymer and polyolefins |
PL3126411T3 (en) * | 2014-04-04 | 2018-04-30 | Borealis Ag | Heterophasic propylene copolymer with low extractables |
US10577492B2 (en) | 2015-08-06 | 2020-03-03 | Basell Poliolefine Italia S.R.L. | Composition comprising propylene-ethylene-1-butene terpolymers |
US10479849B2 (en) | 2015-11-02 | 2019-11-19 | Braskem America, Inc. | Low emission propylene-based polymer resins |
KR102061282B1 (en) | 2016-03-18 | 2019-12-31 | 주식회사 엘지화학 | Polypropylene |
ES2713267T3 (en) | 2016-10-17 | 2019-05-20 | Borealis Ag | Composite of fiber reinforced polypropylene |
EP3551695B1 (en) * | 2016-12-12 | 2023-09-06 | SABIC Global Technologies B.V. | Pellet comprising thermoplastic polymer sheath surrounding glass filaments having reduced emissions |
EP3568430A4 (en) | 2017-01-10 | 2020-07-01 | Celanese International Corporation | Long fiber-reinforced propylene composition for use in a thin part |
CN110291140A (en) * | 2017-01-10 | 2019-09-27 | 国际人造丝公司 | The propylene compositions of high flow fiber enhancing with low emission |
US11149100B2 (en) | 2017-11-06 | 2021-10-19 | Exxonmobil Chemical Patents Inc. | Propylene-based impact copolymers and process and apparatus for production |
CN111527141B (en) * | 2017-12-22 | 2024-03-15 | 博禄塑料(上海)有限公司 | Soft polyolefin composition |
EP3505566A1 (en) * | 2017-12-28 | 2019-07-03 | Borealis AG | Cable jacket |
US20230235105A1 (en) * | 2020-07-17 | 2023-07-27 | Exxonmobil Chemical Patents Inc. | Polymers with low levels of volatile organic compounds and methods of making such polymers |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0368613A (en) * | 1989-08-08 | 1991-03-25 | Chisso Corp | Production of propylene-olefin block copolymer |
JPH0415241A (en) * | 1990-05-08 | 1992-01-20 | Chisso Corp | Production of polypropylene composition |
WO1992019658A1 (en) * | 1991-05-09 | 1992-11-12 | Neste Oy | Coarse grained polyolefin, production thereof and a procatalyst containing a transesterification product between a lower alcohol and dioctylphthalate used therefore |
EP1236769A1 (en) * | 2001-02-21 | 2002-09-04 | Borealis Technology Oy | Heterophasic propylene polymer |
US20060217501A1 (en) * | 2005-03-25 | 2006-09-28 | Migone Ruben A | Process for production of propylene homopolymers |
EP1717269A1 (en) * | 2005-04-28 | 2006-11-02 | Borealis Technology Oy | Alpha-olefin homo-or copolymer compositions |
Family Cites Families (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FI80055C (en) | 1986-06-09 | 1990-04-10 | Neste Oy | Process for preparing catalytic components for polymerization of olefins |
FI86866C (en) | 1990-12-19 | 1992-10-26 | Neste Oy | FOERFARANDE FOER MODIFIERING AV CATALYSTATOR AVSEDDA FOER POLYMERISATION AV OLEFINER |
FI86867C (en) | 1990-12-28 | 1992-10-26 | Neste Oy | FLERSTEGSPROCESS FOR FRAMSTAELLNING AV POLYETEN |
FI88047C (en) | 1991-05-09 | 1993-03-25 | Neste Oy | Catalyst-based catalyst for polymerization of olivines |
US6410663B2 (en) | 1992-06-08 | 2002-06-25 | Fina Technology, Inc. | Electron donors in a Ziegler-Natta catalyst for the production of high melt flow copolymers |
TW354792B (en) | 1993-08-13 | 1999-03-21 | Mitsui Petrochemical Ind | Olefin polymerization catalyst and process for preparing polypropylene and propylene block copolymer |
DE69821866T2 (en) | 1997-04-24 | 2004-12-16 | Mitsui Chemicals, Inc. | CRYSTALLINE POLYPROPYLENE RESIN COMPOSITION |
DE19718900A1 (en) | 1997-05-05 | 1998-11-12 | Targor Gmbh | Polypropylene molding compound with excellent stiffness-toughness relation |
FI111848B (en) | 1997-06-24 | 2003-09-30 | Borealis Tech Oy | Process and equipment for the preparation of homopolymers and copolymers of propylene |
FI974175A (en) * | 1997-11-07 | 1999-05-08 | Borealis As | Process for producing polypropylene |
US6825280B1 (en) | 1998-06-05 | 2004-11-30 | Japan Polychem Corporation | Propylene block copolymer and propylene resin composition |
JP4480116B2 (en) | 1998-11-03 | 2010-06-16 | バセルテック ユーエスエイ インコーポレイテッド | Polyolefin composition with a balance between rigidity and impact strength |
FI991057A0 (en) | 1999-05-07 | 1999-05-07 | Borealis As | High stiffness propylene polymers and process for their preparation |
HUP0104592A3 (en) * | 1999-09-14 | 2003-08-28 | Baselltech Usa Inc Wilmington | Impact-resistant polyolefin compositions |
WO2001036502A1 (en) | 1999-11-12 | 2001-05-25 | Borealis Technology Oy | Heterophasic copolymers |
CN100564400C (en) * | 2001-05-29 | 2009-12-02 | 联合碳化化学及塑料技术有限责任公司 | Olefin Polymerization catalyst compositions and preparation method |
ATE321080T1 (en) | 2002-04-18 | 2006-04-15 | Borealis Gmbh | POLYPROPYLENE MIXTURE WITH IMPROVED MECHANICAL PROPERTIES |
ES2309123T3 (en) | 2002-05-22 | 2008-12-16 | Borealis Technology Oy | EMISSION ITEMS REDUCED FROM REINFORCED POLYPROPYLENE WITH LONG FIBER. |
US20060052541A1 (en) | 2002-06-25 | 2006-03-09 | Erling Hagen | Polyolefin with improved scratch resistance and process for producing the same |
CN1294160C (en) | 2002-07-24 | 2007-01-10 | 巴塞尔聚烯烃股份有限公司 | At least two-stage process for preparing propylene polymer compositions |
AU2003257555A1 (en) * | 2002-08-19 | 2004-03-03 | Ube Industries, Ltd. | CATALYSTS FOR POLYMERIZATION OR COPOLYMERIZATION OF Alpha-OLEFINS, CATALYST COMPONENTS THEREOF, AND PROCESSES FOR POLYMERIZATION OF Alpha-OLEFINS WITH THE CATALYSTS |
EP1484343A1 (en) | 2003-06-06 | 2004-12-08 | Universiteit Twente | Process for the catalytic polymerization of olefins, a reactor system and its use in the same process |
JP4137736B2 (en) | 2003-07-28 | 2008-08-20 | 宇部興産株式会社 | Olefin polymerization catalyst |
CA2534524A1 (en) * | 2003-08-05 | 2005-02-17 | Basell Poliolefine Italia S.R.L. | Polyolefin articles |
ATE382466T1 (en) | 2003-11-28 | 2008-01-15 | Borealis Tech Oy | METHOD FOR REMOVAL OF VOLATILE COMPONENTS FROM A FILLED THERMOPLASTIC POLYMER |
US20080293898A1 (en) | 2004-07-28 | 2008-11-27 | Mitsui Chemicals, Inc. | Catalyst for Olefin Polymerization and Polymerization Method Using the Same |
JP2006096936A (en) | 2004-09-30 | 2006-04-13 | Sumitomo Chemical Co Ltd | alpha-OLEFIN POLYMERIZATION CATALYST AND METHOD FOR PRODUCING alpha-OLEFIN POLYMER |
EP1874530A2 (en) | 2005-04-28 | 2008-01-09 | Basell Poliolefine Italia S.r.l. | Reinforced polypropylene pipe |
EP2226337A1 (en) * | 2009-03-02 | 2010-09-08 | Borealis AG | Process for the production of polypropylene random copolymers for injection moulding applications |
-
2008
- 2008-12-18 EP EP08873974.3A patent/EP2283072B2/en active Active
- 2008-12-18 WO PCT/EP2008/067858 patent/WO2009129873A1/en active Application Filing
- 2008-12-18 US US12/736,586 patent/US9255166B2/en active Active
- 2008-12-18 BR BRPI0822601-6A patent/BRPI0822601B1/en active IP Right Grant
- 2008-12-18 AT AT08873974T patent/ATE551395T1/en active
- 2008-12-18 CN CN2008801289613A patent/CN102015879B/en active Active
- 2008-12-18 RU RU2010143172/04A patent/RU2470946C2/en active
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0368613A (en) * | 1989-08-08 | 1991-03-25 | Chisso Corp | Production of propylene-olefin block copolymer |
JPH0415241A (en) * | 1990-05-08 | 1992-01-20 | Chisso Corp | Production of polypropylene composition |
WO1992019658A1 (en) * | 1991-05-09 | 1992-11-12 | Neste Oy | Coarse grained polyolefin, production thereof and a procatalyst containing a transesterification product between a lower alcohol and dioctylphthalate used therefore |
EP1236769A1 (en) * | 2001-02-21 | 2002-09-04 | Borealis Technology Oy | Heterophasic propylene polymer |
US20060217501A1 (en) * | 2005-03-25 | 2006-09-28 | Migone Ruben A | Process for production of propylene homopolymers |
EP1717269A1 (en) * | 2005-04-28 | 2006-11-02 | Borealis Technology Oy | Alpha-olefin homo-or copolymer compositions |
Non-Patent Citations (1)
Title |
---|
DATABASE WPI Week 199209, Derwent World Patents Index; AN 1992-069948, XP002498084 * |
Cited By (54)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2010100098A1 (en) * | 2009-03-02 | 2010-09-10 | Borealis Ag | Process for the production of propylene random copolymers for injection moulding applications |
EP2226337A1 (en) * | 2009-03-02 | 2010-09-08 | Borealis AG | Process for the production of polypropylene random copolymers for injection moulding applications |
US8822021B2 (en) | 2009-03-02 | 2014-09-02 | Borealis Ag | Process for the production of propylene random copolymers for injection moulding applications |
US8569412B2 (en) | 2009-06-22 | 2013-10-29 | Borealis Ag | Heterophasic polypropylene copolymer composition |
WO2010149529A1 (en) * | 2009-06-22 | 2010-12-29 | Borealis Ag | Heterophasic polypropylene copolymer composition |
WO2010149546A1 (en) * | 2009-06-22 | 2010-12-29 | Borealis Ag | Stabilized polypropylene-talc composite |
EP2275485A1 (en) * | 2009-06-22 | 2011-01-19 | Borealis AG | Heterophasic polypropylene copolymer composition |
US8871834B2 (en) | 2009-06-22 | 2014-10-28 | Borealis Ag | Stabilized polypropylene-talc composite |
US8716387B2 (en) | 2009-06-22 | 2014-05-06 | Borealis Ag | Heterophasic polypropylene copolymer composition |
EP2397517A1 (en) | 2010-06-16 | 2011-12-21 | Borealis AG | Propylene polymer compositions having superior hexane extractables/impact balance |
WO2011157734A1 (en) | 2010-06-16 | 2011-12-22 | Borealis Ag | Propylene polymer composition having superior hexane extractables/impact balance |
CN102432701A (en) * | 2010-09-29 | 2012-05-02 | 中国石油化工股份有限公司 | Catalyst for olefin polymerization |
EA022161B1 (en) * | 2010-11-12 | 2015-11-30 | Бореалис Аг | Soft heterophasic propylene copolymers |
WO2012062735A1 (en) * | 2010-11-12 | 2012-05-18 | Borealis Ag | Improved process for polymerising propylene |
EA024017B1 (en) * | 2010-11-12 | 2016-08-31 | Бореалис Аг | Improved process for polymerising propylene |
WO2012062736A1 (en) * | 2010-11-12 | 2012-05-18 | Borealis Ag | Soft heterophasic propylene copolymers |
EP2452975A1 (en) * | 2010-11-12 | 2012-05-16 | Borealis AG | Soft heterophasic propylene copolymers |
CN103201338B (en) * | 2010-11-12 | 2015-07-01 | 博里利斯股份公司 | Soft heterophasic propylene copolymers |
CN103201338A (en) * | 2010-11-12 | 2013-07-10 | 博里利斯股份公司 | Soft heterophasic propylene copolymers |
WO2012062738A1 (en) | 2010-11-12 | 2012-05-18 | Borealis Ag | Improved process for producing heterophasic propylene copolymers |
EP2452956A1 (en) * | 2010-11-12 | 2012-05-16 | Borealis AG | Improved process for polymerising propylene |
EP2452957A1 (en) | 2010-11-12 | 2012-05-16 | Borealis AG | Improved process for producing heterophasic propylene copolymers |
CN103403087B (en) * | 2011-02-28 | 2015-04-22 | 博里利斯股份公司 | Heterophasic polyolefin composition having improved flowability and impact strength |
CN103403087A (en) * | 2011-02-28 | 2013-11-20 | 博里利斯股份公司 | Heterophasic polyolefin composition having improved flowability and impact strength |
WO2012116719A1 (en) | 2011-02-28 | 2012-09-07 | Borealis Ag | Heterophasic polyolefin composition having improved flowability and impact strength |
WO2012116718A1 (en) | 2011-02-28 | 2012-09-07 | Borealis Ag | Heterophasic polyolefin composition having improved flowability and impact strength |
EP2492310A1 (en) | 2011-02-28 | 2012-08-29 | Borealis AG | Heterophasic polyolefin composition having improved flowability and impact strength |
EP2492309A1 (en) | 2011-02-28 | 2012-08-29 | Borealis AG | Heterophasic polyolefin composition having improved flowability and impact strength |
EP2666817A1 (en) * | 2012-05-24 | 2013-11-27 | Borealis AG | Soft heterophasic polyolefin composition having low C6 extractables |
US10072139B2 (en) | 2012-09-19 | 2018-09-11 | Saudi Basic Industries Corporation | Process for the preparation of a composition comprising heterophasic propylene co-polymer and talc |
EP3071607B1 (en) | 2013-11-22 | 2018-05-09 | Borealis AG | Low emission propylene homopolymer |
EP3212711B1 (en) | 2014-10-27 | 2020-03-04 | Borealis AG | Heterophasic polypropylene with improved stiffness/impact balance |
WO2016066446A1 (en) * | 2014-10-27 | 2016-05-06 | Borealis Ag | Heterophasic polypropylene with improved stiffness/impact balance |
EP3015503A1 (en) | 2014-10-27 | 2016-05-04 | Borealis AG | Heterophasic polypropylene with improved stiffness/impact balance |
US10308795B2 (en) | 2014-10-27 | 2019-06-04 | Borealis Ag | Heterophasic polypropylene with improved stiffness/impact balance |
EP3307820B1 (en) | 2015-06-12 | 2019-10-02 | SABIC Global Technologies B.V. | Process for manufacture of low emission polypropylene |
WO2016198344A1 (en) | 2015-06-12 | 2016-12-15 | Sabic Global Technologies B.V. | Process for manufacture of low emission polypropylene |
US10435552B2 (en) | 2015-06-12 | 2019-10-08 | Sabic Global Technologies B.V. | Process for manufacture of low emission polypropylene |
WO2017148970A1 (en) | 2016-03-04 | 2017-09-08 | Borealis Ag | High flow heterophasic polyolefin composition having improved stiffness/impact balance |
US10759931B2 (en) | 2016-03-04 | 2020-09-01 | Borealis Ag | High flow heterophasic polyolefin compositions having improved stiffness/impact balance |
KR20190017020A (en) * | 2016-06-24 | 2019-02-19 | 보레알리스 아게 | Novel polypropylene compositions with low fogging |
WO2017220556A1 (en) * | 2016-06-24 | 2017-12-28 | Borealis Ag | Novel polypropylene compositions with low fogging |
EA038637B1 (en) * | 2016-06-24 | 2021-09-27 | Бореалис Аг | Novel polypropylene compositions with low fogging |
US10781304B2 (en) | 2016-06-24 | 2020-09-22 | Borealis Ag | Polypropylene compositions with low fogging |
EP3260489A1 (en) * | 2016-06-24 | 2017-12-27 | Borealis AG | Novel polypropylene compositions with low fogging |
KR102135556B1 (en) | 2016-06-24 | 2020-07-22 | 보레알리스 아게 | Novel polypropylene composition with low fogging |
CN109153830A (en) * | 2016-06-28 | 2019-01-04 | 博里利斯股份公司 | Soft and transparent polypropene composition |
US11370904B2 (en) | 2017-06-29 | 2022-06-28 | Borealis Ag | Process for preparing a polypropylene composition |
US11447623B2 (en) | 2017-06-29 | 2022-09-20 | Borealis Ag | Process for preparing a polypropylene composition |
EP3645580B1 (en) * | 2017-06-29 | 2022-12-14 | Borealis AG | Process for preparing a polypropylene composition |
US11746223B2 (en) | 2017-06-29 | 2023-09-05 | Borealis Ag | Process for preparing a polypropylene composition |
US11441024B2 (en) | 2017-12-14 | 2022-09-13 | Borealis Ag | Process for preparing a polypropylene composition |
WO2019162932A1 (en) | 2018-02-20 | 2019-08-29 | Carmel Olefins Ltd. | Polypropylene impact copolymers with reduced emission of volatiles |
WO2021045889A1 (en) * | 2019-09-05 | 2021-03-11 | Exxonmobil Chemical Patents Inc. | Processes for producing polyolefins and impact copolymers with broad molecular weight distribution and high stiffness |
Also Published As
Publication number | Publication date |
---|---|
CN102015879B (en) | 2013-11-20 |
CN102015879A (en) | 2011-04-13 |
EP2283072B2 (en) | 2018-07-18 |
RU2010143172A (en) | 2012-05-27 |
US9255166B2 (en) | 2016-02-09 |
RU2470946C2 (en) | 2012-12-27 |
EP2283072B1 (en) | 2012-03-28 |
ATE551395T1 (en) | 2012-04-15 |
BRPI0822601A2 (en) | 2020-01-21 |
BRPI0822601B1 (en) | 2020-12-01 |
EP2283072A1 (en) | 2011-02-16 |
US20110034634A1 (en) | 2011-02-10 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US9255166B2 (en) | High purity heterophasic propylene copolymers | |
EP2397517B1 (en) | Propylene polymer compositions having superior hexane extractables/impact balance | |
EP2243803B1 (en) | Tough composition for food applications | |
EP2638108B1 (en) | Soft heterophasic propylene copolymers | |
AU2010305546B2 (en) | Glass fibre composite of improved processability | |
US10253171B2 (en) | Thermoplastic polyolefins with high flowability and excellent surface quality produced by a multistage process | |
EP2638109B1 (en) | Process for preparing heterophasic propylene copolymers with improved stiffness/impact/flowability balance | |
EP2415831A1 (en) | Heterophasic propylene copolymer with excellent impact/stiffness balance | |
EP2638079B1 (en) | Improved process for producing heterophasic propylene copolymers | |
WO2013010877A1 (en) | Heterophasic polypropylene with low clte and high stiffness | |
WO2019063746A1 (en) | Reinforced polypropylene composition |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 200880128961.3 Country of ref document: CN |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 08873974 Country of ref document: EP Kind code of ref document: A1 |
|
DPE1 | Request for preliminary examination filed after expiration of 19th month from priority date (pct application filed from 20040101) | ||
WWE | Wipo information: entry into national phase |
Ref document number: 7433/DELNP/2010 Country of ref document: IN Ref document number: 12736586 Country of ref document: US |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2008873974 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2010143172 Country of ref document: RU |
|
ENP | Entry into the national phase |
Ref document number: PI0822601 Country of ref document: BR Kind code of ref document: A2 Effective date: 20101025 |