CA2456951A1 - Process for the preparation of ethylene copolymers - Google Patents
Process for the preparation of ethylene copolymers Download PDFInfo
- Publication number
- CA2456951A1 CA2456951A1 CA002456951A CA2456951A CA2456951A1 CA 2456951 A1 CA2456951 A1 CA 2456951A1 CA 002456951 A CA002456951 A CA 002456951A CA 2456951 A CA2456951 A CA 2456951A CA 2456951 A1 CA2456951 A1 CA 2456951A1
- Authority
- CA
- Canada
- Prior art keywords
- dimethoxypropane
- methyl
- ethylene
- weight
- ethyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 238000000034 method Methods 0.000 title claims abstract description 52
- 229920001038 ethylene copolymer Polymers 0.000 title claims abstract description 28
- 238000002360 preparation method Methods 0.000 title claims abstract description 21
- 239000003054 catalyst Substances 0.000 claims abstract description 53
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 33
- 239000005977 Ethylene Substances 0.000 claims abstract description 33
- 150000001875 compounds Chemical class 0.000 claims abstract description 21
- 239000011949 solid catalyst Substances 0.000 claims abstract description 17
- 229910052749 magnesium Inorganic materials 0.000 claims abstract description 16
- 150000002430 hydrocarbons Chemical group 0.000 claims abstract description 14
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 12
- 229920001577 copolymer Polymers 0.000 claims abstract description 12
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 11
- 125000005842 heteroatom Chemical group 0.000 claims abstract description 10
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 9
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 9
- 238000009826 distribution Methods 0.000 claims abstract description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 7
- 238000007334 copolymerization reaction Methods 0.000 claims abstract description 6
- 150000002367 halogens Chemical class 0.000 claims abstract description 6
- 239000000203 mixture Substances 0.000 claims description 43
- 229920000642 polymer Polymers 0.000 claims description 26
- -1 magnesium halide Chemical class 0.000 claims description 25
- 239000011777 magnesium Substances 0.000 claims description 17
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 14
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 12
- 150000003609 titanium compounds Chemical class 0.000 claims description 12
- 239000004215 Carbon black (E152) Substances 0.000 claims description 11
- 238000004132 cross linking Methods 0.000 claims description 11
- 229930195733 hydrocarbon Natural products 0.000 claims description 11
- 239000010936 titanium Substances 0.000 claims description 11
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 claims description 11
- 229920001155 polypropylene Polymers 0.000 claims description 8
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 6
- 150000004291 polyenes Chemical class 0.000 claims description 6
- 229920000098 polyolefin Polymers 0.000 claims description 6
- SHFQQELHDBUGFP-UHFFFAOYSA-N 1-methoxy-2-(methoxymethyl)-2-methyldecane Chemical compound CCCCCCCCC(C)(COC)COC SHFQQELHDBUGFP-UHFFFAOYSA-N 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 239000008096 xylene Substances 0.000 claims description 4
- ORXXDGPJWPABGK-UHFFFAOYSA-N 1-methoxy-2-(methoxymethyl)-2-methyldodecane Chemical compound CCCCCCCCCCC(C)(COC)COC ORXXDGPJWPABGK-UHFFFAOYSA-N 0.000 claims description 3
- RNKBPVXSXIYBDE-UHFFFAOYSA-N 1-methoxy-2-(methoxymethyl)-2-methylheptane Chemical group CCCCCC(C)(COC)COC RNKBPVXSXIYBDE-UHFFFAOYSA-N 0.000 claims description 3
- WZRLFGQMBUEBFN-UHFFFAOYSA-N 1-methoxy-2-(methoxymethyl)-2-methylnonane Chemical compound CCCCCCCC(C)(COC)COC WZRLFGQMBUEBFN-UHFFFAOYSA-N 0.000 claims description 3
- IAVAUPTWVSKPSI-UHFFFAOYSA-N 1-methoxy-2-(methoxymethyl)-2-methyloctane Chemical compound CCCCCCC(C)(COC)COC IAVAUPTWVSKPSI-UHFFFAOYSA-N 0.000 claims description 3
- IRMJSPFAVRVOND-UHFFFAOYSA-N 3,3-bis(methoxymethyl)decane Chemical compound CCCCCCCC(CC)(COC)COC IRMJSPFAVRVOND-UHFFFAOYSA-N 0.000 claims description 3
- IAYMPZHMWBPMSU-UHFFFAOYSA-N 3,3-bis(methoxymethyl)nonane Chemical compound CCCCCCC(CC)(COC)COC IAYMPZHMWBPMSU-UHFFFAOYSA-N 0.000 claims description 3
- AAFYFJQRBBFOHQ-UHFFFAOYSA-N 3,3-bis(methoxymethyl)octane Chemical compound CCCCCC(CC)(COC)COC AAFYFJQRBBFOHQ-UHFFFAOYSA-N 0.000 claims description 3
- MNPBCGBQUSWAHB-UHFFFAOYSA-N 3,3-bis(methoxymethyl)tridecane Chemical compound CCCCCCCCCCC(CC)(COC)COC MNPBCGBQUSWAHB-UHFFFAOYSA-N 0.000 claims description 3
- LFVWNDZQEDDTBX-UHFFFAOYSA-N 3,3-bis(methoxymethyl)undecane Chemical compound CCCCCCCCC(CC)(COC)COC LFVWNDZQEDDTBX-UHFFFAOYSA-N 0.000 claims description 3
- 229910010062 TiCl3 Inorganic materials 0.000 claims description 3
- YONPGGFAJWQGJC-UHFFFAOYSA-K titanium(iii) chloride Chemical compound Cl[Ti](Cl)Cl YONPGGFAJWQGJC-UHFFFAOYSA-K 0.000 claims description 3
- NDAOWAVNIYQCLK-UHFFFAOYSA-N 3,3-bis(methoxymethyl)heptane Chemical compound CCCCC(CC)(COC)COC NDAOWAVNIYQCLK-UHFFFAOYSA-N 0.000 claims description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 2
- 229920005629 polypropylene homopolymer Polymers 0.000 claims description 2
- 125000006527 (C1-C5) alkyl group Chemical group 0.000 claims 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 claims 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 42
- 238000006116 polymerization reaction Methods 0.000 description 41
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 16
- 238000006243 chemical reaction Methods 0.000 description 13
- 238000003756 stirring Methods 0.000 description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 11
- 239000007791 liquid phase Substances 0.000 description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- 239000012071 phase Substances 0.000 description 10
- 239000000047 product Substances 0.000 description 10
- 229910003074 TiCl4 Inorganic materials 0.000 description 9
- 239000007788 liquid Substances 0.000 description 9
- 238000004073 vulcanization Methods 0.000 description 9
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 8
- 229920001971 elastomer Polymers 0.000 description 8
- 239000007787 solid Substances 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 238000012512 characterization method Methods 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 7
- 239000000806 elastomer Substances 0.000 description 7
- 229920001198 elastomeric copolymer Polymers 0.000 description 6
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 239000004743 Polypropylene Substances 0.000 description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 239000001294 propane Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 4
- BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 description 3
- 239000004606 Fillers/Extenders Substances 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000001336 alkenes Chemical class 0.000 description 3
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 239000003431 cross linking reagent Substances 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 238000010348 incorporation Methods 0.000 description 3
- 229920000092 linear low density polyethylene Polymers 0.000 description 3
- 239000004707 linear low-density polyethylene Substances 0.000 description 3
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- 238000001228 spectrum Methods 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 2
- FUDNBFMOXDUIIE-UHFFFAOYSA-N 3,7-dimethylocta-1,6-diene Chemical compound C=CC(C)CCC=C(C)C FUDNBFMOXDUIIE-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 238000002083 X-ray spectrum Methods 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000000113 differential scanning calorimetry Methods 0.000 description 2
- MGWAVDBGNNKXQV-UHFFFAOYSA-N diisobutyl phthalate Chemical compound CC(C)COC(=O)C1=CC=CC=C1C(=O)OCC(C)C MGWAVDBGNNKXQV-UHFFFAOYSA-N 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 150000002009 diols Chemical class 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 238000007429 general method Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 150000004820 halides Chemical class 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical class ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 2
- 229910052809 inorganic oxide Inorganic materials 0.000 description 2
- 229910001629 magnesium chloride Inorganic materials 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000012265 solid product Substances 0.000 description 2
- 239000012798 spherical particle Substances 0.000 description 2
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- OJOWICOBYCXEKR-APPZFPTMSA-N (1S,4R)-5-ethylidenebicyclo[2.2.1]hept-2-ene Chemical compound CC=C1C[C@@H]2C[C@@H]1C=C2 OJOWICOBYCXEKR-APPZFPTMSA-N 0.000 description 1
- DMGCMUYMJFRQSK-AEJSXWLSSA-N (1s,4s,5r)-5-prop-1-en-2-ylbicyclo[2.2.1]hept-2-ene Chemical compound C1[C@@H]2[C@H](C(=C)C)C[C@H]1C=C2 DMGCMUYMJFRQSK-AEJSXWLSSA-N 0.000 description 1
- VYXHVRARDIDEHS-QGTKBVGQSA-N (1z,5z)-cycloocta-1,5-diene Chemical compound C\1C\C=C/CC\C=C/1 VYXHVRARDIDEHS-QGTKBVGQSA-N 0.000 description 1
- PRBHEGAFLDMLAL-GQCTYLIASA-N (4e)-hexa-1,4-diene Chemical compound C\C=C\CC=C PRBHEGAFLDMLAL-GQCTYLIASA-N 0.000 description 1
- PRBHEGAFLDMLAL-XQRVVYSFSA-N (4z)-hexa-1,4-diene Chemical compound C\C=C/CC=C PRBHEGAFLDMLAL-XQRVVYSFSA-N 0.000 description 1
- MFWFDRBPQDXFRC-LNTINUHCSA-N (z)-4-hydroxypent-3-en-2-one;vanadium Chemical compound [V].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O MFWFDRBPQDXFRC-LNTINUHCSA-N 0.000 description 1
- 0 **N(**=C)N Chemical compound **N(**=C)N 0.000 description 1
- MFEWNFVBWPABCX-UHFFFAOYSA-N 1,1,2,2-tetraphenylethane-1,2-diol Chemical compound C=1C=CC=CC=1C(C(O)(C=1C=CC=CC=1)C=1C=CC=CC=1)(O)C1=CC=CC=C1 MFEWNFVBWPABCX-UHFFFAOYSA-N 0.000 description 1
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
- RELMFMZEBKVZJC-UHFFFAOYSA-N 1,2,3-trichlorobenzene Chemical compound ClC1=CC=CC(Cl)=C1Cl RELMFMZEBKVZJC-UHFFFAOYSA-N 0.000 description 1
- CHRJZRDFSQHIFI-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;styrene Chemical compound C=CC1=CC=CC=C1.C=CC1=CC=CC=C1C=C CHRJZRDFSQHIFI-UHFFFAOYSA-N 0.000 description 1
- QWUWMCYKGHVNAV-UHFFFAOYSA-N 1,2-dihydrostilbene Chemical compound C=1C=CC=CC=1CCC1=CC=CC=C1 QWUWMCYKGHVNAV-UHFFFAOYSA-N 0.000 description 1
- GWQOYRSARAWVTC-UHFFFAOYSA-N 1,4-bis(2-tert-butylperoxypropan-2-yl)benzene Chemical compound CC(C)(C)OOC(C)(C)C1=CC=C(C(C)(C)OOC(C)(C)C)C=C1 GWQOYRSARAWVTC-UHFFFAOYSA-N 0.000 description 1
- PRBHEGAFLDMLAL-UHFFFAOYSA-N 1,5-Hexadiene Natural products CC=CCC=C PRBHEGAFLDMLAL-UHFFFAOYSA-N 0.000 description 1
- KHMYDAWNGSLESQ-UHFFFAOYSA-N 1,7-bis(furan-2-yl)hepta-2,5-dien-4-one Chemical compound C=1C=COC=1CC=CC(=O)C=CCC1=CC=CO1 KHMYDAWNGSLESQ-UHFFFAOYSA-N 0.000 description 1
- HOEFIGOFJSMARD-UHFFFAOYSA-N 1-methylcycloocta-1,5-diene Chemical compound CC1=CCCC=CCC1 HOEFIGOFJSMARD-UHFFFAOYSA-N 0.000 description 1
- KYSNRMGJOYWQQR-UHFFFAOYSA-N 11-methyldodeca-1,10-diene Chemical compound CC(C)=CCCCCCCCC=C KYSNRMGJOYWQQR-UHFFFAOYSA-N 0.000 description 1
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 1
- SLQMKNPIYMOEGB-UHFFFAOYSA-N 2-methylhexa-1,5-diene Chemical compound CC(=C)CCC=C SLQMKNPIYMOEGB-UHFFFAOYSA-N 0.000 description 1
- VXEGSRKPIUDPQT-UHFFFAOYSA-N 4-[4-(4-methoxyphenyl)piperazin-1-yl]aniline Chemical compound C1=CC(OC)=CC=C1N1CCN(C=2C=CC(N)=CC=2)CC1 VXEGSRKPIUDPQT-UHFFFAOYSA-N 0.000 description 1
- WRILNOZCTOEFCD-UHFFFAOYSA-N 5,6-dimethylocta-1,6-diene Chemical compound CC=C(C)C(C)CCC=C WRILNOZCTOEFCD-UHFFFAOYSA-N 0.000 description 1
- INYHZQLKOKTDAI-UHFFFAOYSA-N 5-ethenylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(C=C)CC1C=C2 INYHZQLKOKTDAI-UHFFFAOYSA-N 0.000 description 1
- UGJBFMMPNVKBPX-UHFFFAOYSA-N 5-propan-2-ylidenebicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(=C(C)C)CC1C=C2 UGJBFMMPNVKBPX-UHFFFAOYSA-N 0.000 description 1
- KUFDSEQTHICIIF-UHFFFAOYSA-N 6-methylhepta-1,5-diene Chemical compound CC(C)=CCCC=C KUFDSEQTHICIIF-UHFFFAOYSA-N 0.000 description 1
- UCKITPBQPGXDHV-UHFFFAOYSA-N 7-methylocta-1,6-diene Chemical compound CC(C)=CCCCC=C UCKITPBQPGXDHV-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-OUBTZVSYSA-N Carbon-13 Chemical compound [13C] OKTJSMMVPCPJKN-OUBTZVSYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- 229920010126 Linear Low Density Polyethylene (LLDPE) Polymers 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000002168 alkylating agent Substances 0.000 description 1
- 229940100198 alkylating agent Drugs 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000012662 bulk polymerization Methods 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 239000003426 co-catalyst Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 150000002240 furans Chemical class 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 238000012685 gas phase polymerization Methods 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical compound C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 150000002681 magnesium compounds Chemical class 0.000 description 1
- 150000002690 malonic acid derivatives Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 239000012764 mineral filler Substances 0.000 description 1
- 229940078552 o-xylene Drugs 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- MMMNTDFSPSQXJP-UHFFFAOYSA-N orphenadrine citrate Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O.C=1C=CC=C(C)C=1C(OCCN(C)C)C1=CC=CC=C1 MMMNTDFSPSQXJP-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920002589 poly(vinylethylene) polymer Polymers 0.000 description 1
- 230000037048 polymerization activity Effects 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 230000001603 reducing effect Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000005049 silicon tetrachloride Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 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
- 238000012546 transfer Methods 0.000 description 1
- 150000003682 vanadium compounds Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000003643 water by type Substances 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- 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
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
- C08L23/0807—Copolymers of ethene with unsaturated hydrocarbons only containing four or more carbon atoms
- C08L23/0815—Copolymers of ethene with unsaturated hydrocarbons only containing four or more carbon atoms with aliphatic 1-olefins containing one carbon-to-carbon double bond
-
- 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
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
-
- 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
-
- 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
- C08F255/00—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00
-
- 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
- C08F255/00—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00
- C08F255/02—Macromolecular compounds obtained by polymerising monomers on to polymers of hydrocarbons as defined in group C08F10/00 on to polymers of olefins having two or three carbon atoms
-
- 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
- C08L23/16—Ethene-propene or ethene-propene-diene copolymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L51/00—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L51/06—Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
-
- 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
- C08L2314/00—Polymer mixtures characterised by way of preparation
- C08L2314/02—Ziegler natta catalyst
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)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP02077339.6 | 2002-06-13 | ||
| EP02077339 | 2002-06-13 | ||
| PCT/EP2003/005787 WO2003106514A2 (en) | 2002-06-13 | 2003-05-30 | Process for the preparation of ethylene copolymers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2456951A1 true CA2456951A1 (en) | 2003-12-24 |
Family
ID=29724492
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002456951A Abandoned CA2456951A1 (en) | 2002-06-13 | 2003-05-30 | Process for the preparation of ethylene copolymers |
Country Status (12)
| Country | Link |
|---|---|
| US (3) | US7371806B2 (enExample) |
| EP (1) | EP1511778A2 (enExample) |
| JP (1) | JP2005529225A (enExample) |
| CN (1) | CN1659190A (enExample) |
| AR (1) | AR040211A1 (enExample) |
| AU (1) | AU2003242610A1 (enExample) |
| BR (1) | BR0305247A (enExample) |
| CA (1) | CA2456951A1 (enExample) |
| PL (1) | PL372053A1 (enExample) |
| RU (1) | RU2004105852A (enExample) |
| TR (1) | TR200400209T1 (enExample) |
| WO (1) | WO2003106514A2 (enExample) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1376516B1 (en) | 2002-06-26 | 2008-05-21 | Avery Dennison Corporation | Machine direction oriented polymeric films |
| WO2005113672A1 (en) * | 2004-05-21 | 2005-12-01 | Basell Poliolefine Italia S.R.L. | Impact resistant polyolefin compositions |
| CN1670043A (zh) * | 2005-03-07 | 2005-09-21 | 营口市向阳催化剂有限责任公司 | 烯烃聚合用催化剂及其制备和聚合方法 |
| DE602006007572D1 (de) * | 2005-05-12 | 2009-08-13 | Basell Poliolefine Srl | Propylen-ethylen-copolymere und herstellungsverfahren dafür |
| KR101173267B1 (ko) * | 2006-04-06 | 2012-08-10 | 베이징 리서치 인스티튜트 오브 케미컬 인더스트리, 차이나 페트로리움 앤드 케미컬 코포레이션 | 할로겐화마그네슘 부가물, 이로부터 제조되는 올레핀 중합용 촉매 성분 및 촉매 |
| PL2049333T3 (pl) | 2006-06-14 | 2013-07-31 | Avery Dennison Corp | Łatwo dopasowujące się i nadające się do sztancowania zorientowane wzdłużnie materiały do produkcji etykiet, i etykiety oraz sposób ich otrzymywania |
| BRPI0713492A2 (pt) | 2006-06-20 | 2012-01-24 | Avery Dennison Corp | filme polimérico de multi-camadas para rotulagem de adesivos de derretimento a quente e etiqueta e rótulo dos mesmos |
| CN101472961A (zh) * | 2006-06-22 | 2009-07-01 | 巴塞尔聚烯烃意大利有限责任公司 | 基于1,3-二醚的用于烯烃聚合的催化剂组分 |
| WO2007147740A1 (en) * | 2006-06-22 | 2007-12-27 | Basell Poliolefine Italia S.R.L. | Catalyst component for the polymerization of olefins |
| CN101104656B (zh) * | 2006-07-13 | 2010-11-10 | 中国石油化工股份有限公司 | 用于烯烃聚合反应的催化剂组分及其催化剂 |
| US8940653B2 (en) * | 2010-09-30 | 2015-01-27 | Basell Poliolefine Italia S.R.L. | Magnesium dichloride-alcohol adducts and catalyst components obtained therefrom |
| US9676532B2 (en) | 2012-08-15 | 2017-06-13 | Avery Dennison Corporation | Packaging reclosure label for high alcohol content products |
| BR112015015773A2 (pt) | 2012-12-31 | 2017-07-11 | Reliance Industries Ltd | sistema de catalisador ziegler-natta heterogêneo e um processo para polimerização de olefina com uso do mesmo |
| CN106794664B (zh) | 2014-06-02 | 2021-06-18 | 艾利丹尼森公司 | 耐磨强度、透明度和适形性增强的膜 |
| KR102379360B1 (ko) * | 2014-09-11 | 2022-03-25 | 릴라이언스 인더스트리즈 리미티드 | 폴리에틸렌을 제조하기 위한 지글러-나타 촉매 조성물 |
| JP6598285B2 (ja) * | 2014-11-11 | 2019-10-30 | サンアロマー株式会社 | α−オレフィン類の重合方法 |
| EA033278B1 (ru) * | 2014-12-18 | 2019-09-30 | Бореалис Аг | СПОСОБ ПОЛУЧЕНИЯ ТВЕРДОГО КОМПОНЕНТА КАТАЛИЗАТОРА НА ПОДЛОЖКЕ MgCl |
| JP7313344B2 (ja) * | 2017-10-06 | 2023-07-24 | カウンシル オブ サイエンティフィック アンド インダストリアル リサーチ | 高結晶質非絡み合い超高分子量ポリエチレン（ｕｈｍｗｐｅ）の調製のための不均一系プレ触媒およびその調製方法 |
| EP4038110A1 (en) | 2019-10-04 | 2022-08-10 | Borealis AG | Ziegler-natta catalysts for olefin polymerization |
| US12391778B2 (en) | 2019-10-04 | 2025-08-19 | Borealis Ag | Ziegler-natta catalysts for olefin polymerization |
| BR112022021763A2 (pt) | 2020-04-30 | 2022-12-13 | Dow Global Technologies Llc | Sistema pró-catalisador, e, métodos para a síntese de um sistema pró-catalisador e para a produção de um sistema catalisador, sistema catalisador e para a síntese de um polímero de poliolefina |
| PT4036129T (pt) * | 2021-02-02 | 2023-09-11 | Borealis Ag | Película feita a partir de mistura de terpolímero c2c3c4 - copolímero c3c4 e mistura de terpolímero c2c3c4 - copolímero c3c4 |
| JP2025088144A (ja) * | 2023-11-30 | 2025-06-11 | 東邦チタニウム株式会社 | プロピレン系ブロック共重合体の製造方法 |
| CN121021727A (zh) * | 2025-10-31 | 2025-11-28 | 辽宁省轻工设计院有限公司 | 一种复合聚丙烯催化剂的改性方法 |
Family Cites Families (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1603724A (en) * | 1977-05-25 | 1981-11-25 | Montedison Spa | Components and catalysts for the polymerisation of alpha-olefins |
| IT1098272B (it) * | 1978-08-22 | 1985-09-07 | Montedison Spa | Componenti,di catalizzatori e catalizzatori per la polimerizzazione delle alfa-olefine |
| JPS61152753A (ja) * | 1984-12-27 | 1986-07-11 | Nippon Oil Co Ltd | 架橋樹脂組成物 |
| DE3575346D1 (de) | 1985-02-21 | 1990-02-15 | Ivan A S Z Peschl | Vorrichtung zum uebertragen von zu messenden kraeften in ein kraftmessinstrument. |
| JPS63265940A (ja) * | 1987-04-24 | 1988-11-02 | Nippon Oil Co Ltd | 熱可塑性エラストマ−組成物 |
| IT1217744B (it) | 1988-05-31 | 1990-03-30 | Himont Inc | Componenti e catalizzatori per la polimerizzazione di olefine |
| IT1227341B (it) | 1988-09-13 | 1991-04-08 | Ausimont Spa | Composizioni poliolefiniche plasto-elastomeriche e procedimento per la loro preparazione con metodi di vulcanizzazione dinamica |
| IT1227260B (it) * | 1988-09-30 | 1991-03-28 | Himont Inc | Dieteri utilizzabili nella preparazione di catalizzatori ziegler-natta |
| IT1237812B (it) | 1989-12-22 | 1993-06-17 | Himont Inc | Componenti e catalizzatori per la polimerizzazione di olefine |
| JPH03294310A (ja) | 1990-04-13 | 1991-12-25 | Mitsui Petrochem Ind Ltd | エチレン・α―オレフィン共重合体の製造方法 |
| JP2959800B2 (ja) | 1990-04-13 | 1999-10-06 | 三井化学株式会社 | プロピレン系ブロック共重合体の製造方法 |
| JP2945067B2 (ja) | 1990-04-13 | 1999-09-06 | 三井化学株式会社 | プロピレン系ランダム共重合体の製造方法 |
| JP2940991B2 (ja) | 1990-04-13 | 1999-08-25 | 三井化学株式会社 | 低結晶性または非晶性α―オレフィン共重合体の製造方法 |
| US5173536A (en) * | 1990-12-11 | 1992-12-22 | Union Carbide Chemicals & Plastics Technology Corporation | Impact polymer blend |
| IT1246614B (it) | 1991-06-03 | 1994-11-24 | Himont Inc | Procedimento per la polimerizzazione in fase gas delle olefine |
| IT1250731B (it) | 1991-07-31 | 1995-04-21 | Himont Inc | Procedimento per la preparazione di polietilene lineare a bassa densita' |
| IT1254279B (it) * | 1992-03-13 | 1995-09-14 | Montecatini Tecnologie Srl | Procedimento per la polimerizzazione in fase gas delle olefine |
| IT1264679B1 (it) * | 1993-07-07 | 1996-10-04 | Spherilene Srl | Catalizzatori per la (co)polimerizzazione di etilene |
| TW354792B (en) | 1993-08-13 | 1999-03-21 | Mitsui Petrochemical Ind | Olefin polymerization catalyst and process for preparing polypropylene and propylene block copolymer |
| JP3472935B2 (ja) | 1994-02-18 | 2003-12-02 | 三井化学株式会社 | エチレン系重合体およびその製造方法、エチレン重合用固体状チタン触媒成分ならびにエチレン重合用触媒 |
| KR100359370B1 (ko) | 1995-02-07 | 2003-02-11 | 미쓰이 가가쿠 가부시키가이샤 | 올레핀중합체의제조방법 |
| JP3715670B2 (ja) | 1995-02-07 | 2005-11-09 | 三井化学株式会社 | オレフィン重合体組成物の製造方法 |
| JP3529929B2 (ja) | 1996-02-23 | 2004-05-24 | 三井化学株式会社 | オレフィン重合体の製造方法 |
| JPH09227616A (ja) | 1996-02-23 | 1997-09-02 | Mitsui Petrochem Ind Ltd | オレフィン重合体の製造方法 |
| EP0972800A4 (en) | 1997-04-02 | 2004-06-16 | Chisso Corp | MODIFIED OLEFIN (CO) POLYMER COMPOSITION, METHOD FOR THE PRODUCTION THEREOF AND MODIFIED OLEFIN (CO) POLYMER MOLD |
| KR20030029821A (ko) | 2001-06-13 | 2003-04-16 | 바셀 폴리올레핀 이탈리아 에스.피.에이. | 올레핀 (공)중합용 성분 및 촉매 |
| BR0304880A (pt) | 2002-05-29 | 2004-08-03 | Basell Poliolefine Spa | Homopolìmeros ou copolìmeros de buteno-1 e processo para a sua preparação |
| ATE365752T1 (de) | 2002-06-13 | 2007-07-15 | Basell Poliolefine Srl | Ziegler natta katalysator für die polymerisation von olefinen |
-
2003
- 2003-05-30 EP EP03759906A patent/EP1511778A2/en not_active Withdrawn
- 2003-05-30 AU AU2003242610A patent/AU2003242610A1/en not_active Abandoned
- 2003-05-30 CN CN03813529.9A patent/CN1659190A/zh active Pending
- 2003-05-30 CA CA002456951A patent/CA2456951A1/en not_active Abandoned
- 2003-05-30 TR TR2004/00209T patent/TR200400209T1/xx unknown
- 2003-05-30 JP JP2004513343A patent/JP2005529225A/ja not_active Withdrawn
- 2003-05-30 PL PL03372053A patent/PL372053A1/xx not_active Application Discontinuation
- 2003-05-30 RU RU2004105852/04A patent/RU2004105852A/ru not_active Application Discontinuation
- 2003-05-30 US US10/503,104 patent/US7371806B2/en not_active Expired - Fee Related
- 2003-05-30 BR BR0305247-8A patent/BR0305247A/pt not_active Application Discontinuation
- 2003-05-30 WO PCT/EP2003/005787 patent/WO2003106514A2/en not_active Ceased
- 2003-06-12 AR ARP030102103A patent/AR040211A1/es unknown
-
2007
- 2007-11-01 US US11/982,705 patent/US20080182941A1/en not_active Abandoned
- 2007-11-01 US US11/982,706 patent/US20080064836A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| US20080064836A1 (en) | 2008-03-13 |
| PL372053A1 (en) | 2005-07-11 |
| RU2004105852A (ru) | 2005-06-27 |
| EP1511778A2 (en) | 2005-03-09 |
| WO2003106514A3 (en) | 2004-08-05 |
| TR200400209T1 (tr) | 2005-04-21 |
| BR0305247A (pt) | 2004-09-21 |
| AR040211A1 (es) | 2005-03-16 |
| US20050107539A1 (en) | 2005-05-19 |
| CN1659190A (zh) | 2005-08-24 |
| WO2003106514A2 (en) | 2003-12-24 |
| AU2003242610A1 (en) | 2003-12-31 |
| JP2005529225A (ja) | 2005-09-29 |
| US7371806B2 (en) | 2008-05-13 |
| US20080182941A1 (en) | 2008-07-31 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US20080064836A1 (en) | Process for the preparation of ethylene copolymers | |
| US7019078B1 (en) | Dynamically vulcanizable polyolefin composition | |
| FI110107B (fi) | Termoplastinen olefiinipolymeeri ja menetelmä sen valmistamiseksi | |
| CN101039967B (zh) | 低全同立构规整度丁烯-1均聚物或共聚物 | |
| AU2002308130B2 (en) | Soft polyolefin compositions | |
| US6268438B1 (en) | Thermoplastic elastomeric compositions | |
| US6251998B1 (en) | Hydrosilylation crosslinking of thermoplastic elastomer | |
| CN102066478B (zh) | 通过多级方法生产的具有高流动性和优异的表面质量的热塑性聚烯烃 | |
| US6121383A (en) | Thermosplastic vulcanizates from blends of a polypropylene and elastic α-olefin/cyclic olefin copolymers | |
| JP2008195933A (ja) | 軟質プロピレン系樹脂組成物 | |
| CA2583225A1 (en) | Elastomeric polyolefin compositions | |
| CA2610030A1 (en) | Polyolefinic compositions having good whitening resistance | |
| US6001933A (en) | Flexible polypropylene resins, propylene based elastomer compositions and process for production of olefin polymers | |
| WO1999020663A2 (en) | High impact, flexural moduli polymeric materials formed using sequential donors | |
| EP1948703B1 (en) | Propylene-ethylene copolymers and process for their preparation | |
| EP1634919A1 (en) | Improved thermoplastic vulcanizates | |
| JP3569560B2 (ja) | 無機フィラー強化樹脂組成物 | |
| US3725364A (en) | Process for preparing elastomers of ethylene and c{11 -c{11 {11 {11 alpha olefins | |
| JP3451443B2 (ja) | エチレンのエラストマー共重合体の製法 | |
| JP3151064B2 (ja) | プロピレン系樹脂組成物 | |
| KR20050020996A (ko) | 에틸렌 공중합체의 제조방법 | |
| JP3115409B2 (ja) | プロピレン系樹脂組成物 | |
| JP3151052B2 (ja) | プロピレン系樹脂組成物 | |
| JPH03162429A (ja) | 熱可塑性エラストマーの製造方法 | |
| KR20070018922A (ko) | 사출 성형에 적합한 폴리올레핀 마스터배치 및 조성물 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FZDE | Discontinued | ||
| FZDE | Discontinued |
Effective date: 20070530 |