CA2438163A1 - Propylene polymers for films - Google Patents
Propylene polymers for films Download PDFInfo
- Publication number
- CA2438163A1 CA2438163A1 CA002438163A CA2438163A CA2438163A1 CA 2438163 A1 CA2438163 A1 CA 2438163A1 CA 002438163 A CA002438163 A CA 002438163A CA 2438163 A CA2438163 A CA 2438163A CA 2438163 A1 CA2438163 A1 CA 2438163A1
- Authority
- CA
- Canada
- Prior art keywords
- group
- dimethylsilandiylbis
- methyl
- indenyl
- film
- 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
- 229920001155 polypropylene Polymers 0.000 title abstract description 48
- 238000000034 method Methods 0.000 claims abstract description 88
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 74
- 239000000203 mixture Substances 0.000 claims abstract description 52
- 238000009826 distribution Methods 0.000 claims abstract description 49
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 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 43
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 38
- 239000005977 Ethylene Substances 0.000 claims abstract description 38
- 238000004519 manufacturing process Methods 0.000 claims abstract description 32
- 239000012968 metallocene catalyst Substances 0.000 claims abstract description 32
- 239000003054 catalyst Substances 0.000 claims description 71
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 51
- 230000008569 process Effects 0.000 claims description 42
- 229910052726 zirconium Inorganic materials 0.000 claims description 29
- VPGLGRNSAYHXPY-UHFFFAOYSA-L zirconium(2+);dichloride Chemical compound Cl[Zr]Cl VPGLGRNSAYHXPY-UHFFFAOYSA-L 0.000 claims description 17
- 239000012190 activator Substances 0.000 claims description 16
- 239000012632 extractable Substances 0.000 claims description 15
- 239000000463 material Substances 0.000 claims description 14
- 125000005843 halogen group Chemical group 0.000 claims description 13
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims description 10
- 125000005018 aryl alkenyl group Chemical group 0.000 claims description 10
- FLFNHHSXSLXYQB-UHFFFAOYSA-L CC1=CC(C(=CC=C2)C=3C=CC=CC=3)=C2C1[Zr](Cl)(Cl)(=[Si](C)C)C1C(C)=CC2=C1C=CC=C2C1=CC=CC=C1 Chemical compound CC1=CC(C(=CC=C2)C=3C=CC=CC=3)=C2C1[Zr](Cl)(Cl)(=[Si](C)C)C1C(C)=CC2=C1C=CC=C2C1=CC=CC=C1 FLFNHHSXSLXYQB-UHFFFAOYSA-L 0.000 claims description 9
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 9
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
- 125000000041 C6-C10 aryl group Chemical group 0.000 claims description 8
- 125000003118 aryl group Chemical group 0.000 claims description 8
- 125000004122 cyclic group Chemical group 0.000 claims description 8
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 claims description 6
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 claims description 6
- CGELJBSWQTYCIY-UHFFFAOYSA-L [Cl-].[Cl-].CC1=Cc2ccccc2[C@H]1[Zr++]([C@@H]1C(C)=Cc2ccccc12)=[Si](C)C Chemical compound [Cl-].[Cl-].CC1=Cc2ccccc2[C@H]1[Zr++]([C@@H]1C(C)=Cc2ccccc12)=[Si](C)C CGELJBSWQTYCIY-UHFFFAOYSA-L 0.000 claims description 6
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 claims description 6
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 5
- 125000004429 atom Chemical group 0.000 claims description 5
- 238000007334 copolymerization reaction Methods 0.000 claims description 5
- 229910052735 hafnium Inorganic materials 0.000 claims description 5
- 229910052710 silicon Inorganic materials 0.000 claims description 5
- 239000010703 silicon Substances 0.000 claims description 5
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 claims description 4
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 4
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims description 4
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 claims description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 4
- IOEZEGGCMNVLHK-UHFFFAOYSA-L [Cl-].[Cl-].CC1=Cc2cc(C)c(C)cc2C1[Zr++](C1C(C)=Cc2cc(C)c(C)cc12)=[Si](C)C Chemical compound [Cl-].[Cl-].CC1=Cc2cc(C)c(C)cc2C1[Zr++](C1C(C)=Cc2cc(C)c(C)cc12)=[Si](C)C IOEZEGGCMNVLHK-UHFFFAOYSA-L 0.000 claims description 4
- 125000004104 aryloxy group Chemical group 0.000 claims description 4
- 229910052732 germanium Inorganic materials 0.000 claims description 4
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 claims description 4
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 claims description 4
- 229910052719 titanium Inorganic materials 0.000 claims description 4
- 239000010936 titanium Substances 0.000 claims description 4
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 claims description 3
- 125000003860 C1-C20 alkoxy group Chemical group 0.000 claims description 3
- 125000003358 C2-C20 alkenyl group Chemical group 0.000 claims description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 3
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 3
- PNRJUCXJBYLCRR-UHFFFAOYSA-L [Cl-].[Cl-].CC1=Cc2cccc(C)c2C1[Zr++](C1C(C)=Cc2cccc(C)c12)=[Si](C)C Chemical compound [Cl-].[Cl-].CC1=Cc2cccc(C)c2C1[Zr++](C1C(C)=Cc2cccc(C)c12)=[Si](C)C PNRJUCXJBYLCRR-UHFFFAOYSA-L 0.000 claims description 3
- 229910052804 chromium Inorganic materials 0.000 claims description 3
- 239000011651 chromium Substances 0.000 claims description 3
- 125000004407 fluoroaryl group Chemical group 0.000 claims description 3
- 229910052750 molybdenum Inorganic materials 0.000 claims description 3
- 239000011733 molybdenum Substances 0.000 claims description 3
- 229910052715 tantalum Inorganic materials 0.000 claims description 3
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 claims description 3
- 229910052718 tin Inorganic materials 0.000 claims description 3
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 3
- 229910052721 tungsten Inorganic materials 0.000 claims description 3
- 239000010937 tungsten Substances 0.000 claims description 3
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims description 2
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims 2
- AECTWRMNKTVPEM-UHFFFAOYSA-L [Cl-].[Cl-].CC1=C(C(C2=CC=CC=C12)[Zr+2](C1C=CC2=CC=CC=C12)=[SiH2])C Chemical compound [Cl-].[Cl-].CC1=C(C(C2=CC=CC=C12)[Zr+2](C1C=CC2=CC=CC=C12)=[SiH2])C AECTWRMNKTVPEM-UHFFFAOYSA-L 0.000 claims 2
- JQHPURQXTURPDS-UHFFFAOYSA-L [Cl-].[Cl-].C[Si](C)=[Zr++]([C@H]1C=CC2=C1CCCC2)[C@@H]1C=CC2=C1CCCC2 Chemical compound [Cl-].[Cl-].C[Si](C)=[Zr++]([C@H]1C=CC2=C1CCCC2)[C@@H]1C=CC2=C1CCCC2 JQHPURQXTURPDS-UHFFFAOYSA-L 0.000 claims 2
- ABLLXXOPOBEPIU-UHFFFAOYSA-N niobium vanadium Chemical compound [V].[Nb] ABLLXXOPOBEPIU-UHFFFAOYSA-N 0.000 claims 2
- 229920000642 polymer Polymers 0.000 abstract description 167
- 229920001577 copolymer Polymers 0.000 abstract description 32
- 229920001384 propylene homopolymer Polymers 0.000 abstract description 12
- 230000009977 dual effect Effects 0.000 abstract description 6
- 230000002902 bimodal effect Effects 0.000 abstract description 3
- 239000000523 sample Substances 0.000 description 83
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 50
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 45
- 229920001519 homopolymer Polymers 0.000 description 31
- 239000000243 solution Substances 0.000 description 31
- -1 Polypropylene Polymers 0.000 description 29
- 239000000047 product Substances 0.000 description 28
- 238000010348 incorporation Methods 0.000 description 23
- 239000000377 silicon dioxide Substances 0.000 description 21
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 20
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 18
- 150000001450 anions Chemical class 0.000 description 17
- 239000001257 hydrogen Substances 0.000 description 16
- 229910052739 hydrogen Inorganic materials 0.000 description 16
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 15
- 239000002841 Lewis acid Substances 0.000 description 15
- 150000001875 compounds Chemical class 0.000 description 15
- 150000007517 lewis acids Chemical class 0.000 description 15
- 239000011148 porous material Substances 0.000 description 15
- 239000004743 Polypropylene Substances 0.000 description 14
- AQZWEFBJYQSQEH-UHFFFAOYSA-N 2-methyloxaluminane Chemical compound C[Al]1CCCCO1 AQZWEFBJYQSQEH-UHFFFAOYSA-N 0.000 description 13
- 238000012545 processing Methods 0.000 description 13
- 239000000126 substance Substances 0.000 description 13
- 238000002844 melting Methods 0.000 description 11
- 230000008018 melting Effects 0.000 description 11
- 230000008901 benefit Effects 0.000 description 10
- 229910052757 nitrogen Inorganic materials 0.000 description 10
- 239000002243 precursor Substances 0.000 description 10
- 238000012360 testing method Methods 0.000 description 10
- 150000001768 cations Chemical class 0.000 description 9
- 238000005227 gel permeation chromatography Methods 0.000 description 9
- 230000007935 neutral effect Effects 0.000 description 9
- 229920005604 random copolymer Polymers 0.000 description 9
- 239000002904 solvent Substances 0.000 description 9
- 230000004888 barrier function Effects 0.000 description 8
- 238000005259 measurement Methods 0.000 description 8
- 239000002245 particle Substances 0.000 description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 8
- 239000002516 radical scavenger Substances 0.000 description 8
- 239000002002 slurry Substances 0.000 description 8
- 125000000217 alkyl group Chemical group 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 7
- 229920001038 ethylene copolymer Polymers 0.000 description 7
- 230000002349 favourable effect Effects 0.000 description 7
- 239000003446 ligand Substances 0.000 description 7
- 238000011020 pilot scale process Methods 0.000 description 7
- 230000000379 polymerizing effect Effects 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- 241000894007 species Species 0.000 description 7
- 238000004458 analytical method Methods 0.000 description 6
- 229910052801 chlorine Inorganic materials 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 239000007791 liquid phase Substances 0.000 description 6
- 239000000178 monomer Substances 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 239000000460 chlorine Substances 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 238000004806 packaging method and process Methods 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 238000000926 separation method Methods 0.000 description 5
- 238000004260 weight control Methods 0.000 description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
- 238000005481 NMR spectroscopy Methods 0.000 description 4
- 239000007983 Tris buffer Substances 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 4
- 239000013068 control sample Substances 0.000 description 4
- GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 description 4
- 150000002367 halogens Chemical group 0.000 description 4
- 230000001976 improved effect Effects 0.000 description 4
- 229910052809 inorganic oxide Inorganic materials 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 229920000098 polyolefin Polymers 0.000 description 4
- 238000007665 sagging Methods 0.000 description 4
- 239000002356 single layer Substances 0.000 description 4
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 3
- 125000003342 alkenyl group Chemical group 0.000 description 3
- 229910052796 boron Inorganic materials 0.000 description 3
- 238000005266 casting Methods 0.000 description 3
- 238000012512 characterization method Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000010828 elution Methods 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- QDEZCOQKJSRQNN-UHFFFAOYSA-N ethenyl-dimethyl-phenylsilane Chemical compound C=C[Si](C)(C)C1=CC=CC=C1 QDEZCOQKJSRQNN-UHFFFAOYSA-N 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- 238000005194 fractionation Methods 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 239000013628 high molecular weight specie Substances 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 238000011068 loading method Methods 0.000 description 3
- 239000002609 medium Substances 0.000 description 3
- 239000002480 mineral oil Substances 0.000 description 3
- 235000010446 mineral oil Nutrition 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 239000012299 nitrogen atmosphere Substances 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 230000000737 periodic effect Effects 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 229920006254 polymer film Polymers 0.000 description 3
- 229920005629 polypropylene homopolymer Polymers 0.000 description 3
- 238000010926 purge Methods 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
- 229910052723 transition metal Inorganic materials 0.000 description 3
- 150000003624 transition metals Chemical class 0.000 description 3
- OBAJXDYVZBHCGT-UHFFFAOYSA-N tris(pentafluorophenyl)borane Chemical compound FC1=C(F)C(F)=C(F)C(F)=C1B(C=1C(=C(F)C(F)=C(F)C=1F)F)C1=C(F)C(F)=C(F)C(F)=C1F OBAJXDYVZBHCGT-UHFFFAOYSA-N 0.000 description 3
- 239000003039 volatile agent Substances 0.000 description 3
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- BBAAOLXGHYSVPE-UHFFFAOYSA-L CCc1cccc2C(C(C)=Cc12)[Zr](Cl)(Cl)(C1C(C)=Cc2c1cccc2CC)=[Si](C)C Chemical compound CCc1cccc2C(C(C)=Cc12)[Zr](Cl)(Cl)(C1C(C)=Cc2c1cccc2CC)=[Si](C)C BBAAOLXGHYSVPE-UHFFFAOYSA-L 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- 239000002879 Lewis base Substances 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- NDJMNNSJDIFFTH-UHFFFAOYSA-L [Cl-].[Cl-].CC1=CC(C(=CC=C2)C=3C=CC=CC=3)=C2C1[Zr+2]([SiH](C)C)C1C(C)=CC2=C1C=CC=C2C1=CC=CC=C1 Chemical compound [Cl-].[Cl-].CC1=CC(C(=CC=C2)C=3C=CC=CC=3)=C2C1[Zr+2]([SiH](C)C)C1C(C)=CC2=C1C=CC=C2C1=CC=CC=C1 NDJMNNSJDIFFTH-UHFFFAOYSA-L 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 229920006378 biaxially oriented polypropylene Polymers 0.000 description 2
- 239000011127 biaxially oriented polypropylene Substances 0.000 description 2
- 229920001400 block copolymer Polymers 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000000921 elemental analysis Methods 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 239000012634 fragment Substances 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 150000004678 hydrides Chemical class 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 239000013067 intermediate product Substances 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 150000007527 lewis bases Chemical class 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000002667 nucleating agent Substances 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 239000005026 oriented polypropylene Substances 0.000 description 2
- 238000011084 recovery Methods 0.000 description 2
- 230000000630 rising effect Effects 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 229920006300 shrink film Polymers 0.000 description 2
- 239000011949 solid catalyst Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 238000003856 thermoforming Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- UUZYCNJCMNFXIZ-UHFFFAOYSA-N (2,3,4,5,6,7,8-heptafluoronaphthalen-1-yl)boron Chemical compound FC1=C(F)C(F)=C2C([B])=C(F)C(F)=C(F)C2=C1F UUZYCNJCMNFXIZ-UHFFFAOYSA-N 0.000 description 1
- ZOICEQJZAWJHSI-UHFFFAOYSA-N (2,3,4,5,6-pentafluorophenyl)boron Chemical compound [B]C1=C(F)C(F)=C(F)C(F)=C1F ZOICEQJZAWJHSI-UHFFFAOYSA-N 0.000 description 1
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 description 1
- 125000006736 (C6-C20) aryl group Chemical group 0.000 description 1
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 1
- OKICHZSTRJQITD-UHFFFAOYSA-N 5-methylcyclopenta-1,3-diene zirconium(2+) Chemical compound [Zr++].C[c-]1cccc1.C[c-]1cccc1 OKICHZSTRJQITD-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- OJVWBQRZCJLURF-UHFFFAOYSA-L C1=CC=C2C(C3=CC=CC4=C3C=C(C)C4[Zr](Cl)(Cl)(C3C4=C(C(=CC=C4)C=4C5=CC=CC=C5C=CC=4)C=C3C)=[Si](C)C)=CC=CC2=C1 Chemical compound C1=CC=C2C(C3=CC=CC4=C3C=C(C)C4[Zr](Cl)(Cl)(C3C4=C(C(=CC=C4)C=4C5=CC=CC=C5C=CC=4)C=C3C)=[Si](C)C)=CC=CC2=C1 OJVWBQRZCJLURF-UHFFFAOYSA-L 0.000 description 1
- CZPSTFVUNSZYCA-UHFFFAOYSA-L CC(C)c1cc2C(C(C)=Cc2c(c1)C(C)C)[Zr](Cl)(Cl)(C1C(C)=Cc2c1cc(cc2C(C)C)C(C)C)=[Si](C)C Chemical compound CC(C)c1cc2C(C(C)=Cc2c(c1)C(C)C)[Zr](Cl)(Cl)(C1C(C)=Cc2c1cc(cc2C(C)C)C(C)C)=[Si](C)C CZPSTFVUNSZYCA-UHFFFAOYSA-L 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
-
- 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
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F10/04—Monomers containing three or four carbon atoms
- C08F10/06—Propene
-
- 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
- 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
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F297/00—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
- C08F297/06—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type
- C08F297/08—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type polymerising mono-olefins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
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- 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
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
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- 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
- C08L23/14—Copolymers of propene
- C08L23/142—Copolymers of propene at least partially crystalline copolymers of propene with other olefins
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
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- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
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- 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
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- Y10T428/1334—Nonself-supporting tubular film or bag [e.g., pouch, envelope, packet, etc.]
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- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
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- Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
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- Manufacturing & Machinery (AREA)
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- Inorganic Chemistry (AREA)
- Materials Engineering (AREA)
- Crystallography & Structural Chemistry (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Shaping By String And By Release Of Stress In Plastics And The Like (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/800,239 US6576306B2 (en) | 1996-09-04 | 2001-03-06 | Propylene polymers for films |
| US09/800,239 | 2001-03-06 | ||
| PCT/US2002/002469 WO2002070570A2 (en) | 2001-03-06 | 2002-01-28 | Propylene polymers for films |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2438163A1 true CA2438163A1 (en) | 2002-09-12 |
Family
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002438163A Abandoned CA2438163A1 (en) | 2001-03-06 | 2002-01-28 | Propylene polymers for films |
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| Country | Link |
|---|---|
| US (1) | US6576306B2 (enExample) |
| JP (1) | JP2004528420A (enExample) |
| CN (1) | CN1498231A (enExample) |
| AU (1) | AU2002243700A1 (enExample) |
| BR (1) | BR0207885A (enExample) |
| CA (1) | CA2438163A1 (enExample) |
| MX (1) | MXPA03008012A (enExample) |
| WO (1) | WO2002070570A2 (enExample) |
Families Citing this family (65)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7919561B2 (en) * | 1996-09-04 | 2011-04-05 | Exxonmobil Chemical Patents Inc. | Process of producing thermoplastic polymer blends |
| US6921794B2 (en) | 1997-08-12 | 2005-07-26 | Exxonmobil Chemical Patents Inc. | Blends made from propylene ethylene polymers |
| US6635715B1 (en) | 1997-08-12 | 2003-10-21 | Sudhin Datta | Thermoplastic polymer blends of isotactic polypropylene and alpha-olefin/propylene copolymers |
| US7232871B2 (en) | 1997-08-12 | 2007-06-19 | Exxonmobil Chemical Patents Inc. | Propylene ethylene polymers and production process |
| AU4962399A (en) | 1998-07-01 | 2000-01-24 | Exxon Chemical Patents Inc. | Elastic blends comprising crystalline polymer and crystallizable polymers of propylene |
| US20030039826A1 (en) | 2000-03-20 | 2003-02-27 | Sun Edward I. | Conformable and die-cuttable biaxially oriented films and labelstocks |
| JP5156167B2 (ja) | 2001-04-12 | 2013-03-06 | エクソンモービル・ケミカル・パテンツ・インク | プロピレン−エチレンポリマー及び製造法 |
| US6825276B2 (en) * | 2001-04-17 | 2004-11-30 | Pliant Corporation | Nonoriented stiff packaging film with superior tear properties |
| ATE396472T1 (de) | 2002-06-26 | 2008-06-15 | Avery Dennison Corp | Längsorientierte polymere filme |
| US7714070B2 (en) * | 2002-08-27 | 2010-05-11 | Sunoco Chemicals, Inc. | In-reactor produced polypropylene blends |
| US20070167576A1 (en) * | 2002-08-27 | 2007-07-19 | Sehyun Kim | Resin compositions for producing biaxially oriented polypropylene films |
| US20080153997A1 (en) * | 2006-12-20 | 2008-06-26 | Exxonmobil Research And Engineering | Polymer production at supercritical conditions |
| US8008412B2 (en) * | 2002-09-20 | 2011-08-30 | Exxonmobil Chemical Patents Inc. | Polymer production at supersolution conditions |
| AU2003298591A1 (en) * | 2002-09-23 | 2004-05-04 | Johns Hopkins University | Double crystal analyzer linkage |
| US7550528B2 (en) | 2002-10-15 | 2009-06-23 | Exxonmobil Chemical Patents Inc. | Functionalized olefin polymers |
| US7700707B2 (en) | 2002-10-15 | 2010-04-20 | Exxonmobil Chemical Patents Inc. | Polyolefin adhesive compositions and articles made therefrom |
| EP2261292B1 (en) | 2002-10-15 | 2014-07-23 | ExxonMobil Chemical Patents Inc. | Polyolefin adhesive compositions |
| US7259215B2 (en) * | 2002-11-14 | 2007-08-21 | Idemitsu Kosan Co., Ltd. | Process for producing propylene/ethylene block copolymer and propylene/ethylene block copolymer |
| WO2004060994A1 (en) * | 2002-12-17 | 2004-07-22 | Exxonmobil Chemical Patents Inc. | Elastic blends comprising elastic crystalline polymer and crystallizable polymers for ethylene |
| JP2007515512A (ja) * | 2003-11-24 | 2007-06-14 | スリーエム イノベイティブ プロパティズ カンパニー | 二軸延伸ポリプロピレン系接着剤テープフィルムバッキング |
| US7671131B2 (en) * | 2004-03-17 | 2010-03-02 | Dow Global Technologies Inc. | Interpolymers of ethylene/α-olefins blends and profiles and gaskets made therefrom |
| US7622529B2 (en) * | 2004-03-17 | 2009-11-24 | Dow Global Technologies Inc. | Polymer blends from interpolymers of ethylene/alpha-olefin with improved compatibility |
| US7671106B2 (en) * | 2004-03-17 | 2010-03-02 | Dow Global Technologies Inc. | Cap liners, closures and gaskets from multi-block polymers |
| US7579408B2 (en) * | 2004-03-17 | 2009-08-25 | Dow Global Technologies Inc. | Thermoplastic vulcanizate comprising interpolymers of ethylene/α-olefins |
| US7714071B2 (en) * | 2004-03-17 | 2010-05-11 | Dow Global Technologies Inc. | Polymer blends from interpolymers of ethylene/α-olefins and flexible molded articles made therefrom |
| US7514517B2 (en) * | 2004-03-17 | 2009-04-07 | Dow Global Technologies Inc. | Anti-blocking compositions comprising interpolymers of ethylene/α-olefins |
| US7863379B2 (en) * | 2004-03-17 | 2011-01-04 | Dow Global Technologies Inc. | Impact modification of thermoplastics with ethylene/alpha-olefin interpolymers |
| US7795321B2 (en) * | 2004-03-17 | 2010-09-14 | Dow Global Technologies Inc. | Rheology modification of interpolymers of ethylene/α-olefins and articles made therefrom |
| BRPI0513057A (pt) * | 2004-07-08 | 2008-04-22 | Exxonmobil Chem Patents Inc | produção de polìmero em condições supercrìticas |
| GB2420348B (en) * | 2004-10-28 | 2009-11-18 | Exxonmobil Chem Patents Inc | Syndiotactic rich polyolefins |
| KR101257521B1 (ko) * | 2004-11-08 | 2013-04-23 | 미츠비시 가스 가가쿠 가부시키가이샤 | 방향족 폴리아미드 연신 필름 |
| US7473750B2 (en) * | 2004-12-07 | 2009-01-06 | Fina Technology, Inc. | Random copolymers and formulations useful for thermoforming and blow molding applications |
| CN104963085A (zh) * | 2004-12-17 | 2015-10-07 | 埃克森美孚化学专利公司 | 聚合物共混物和由其获得的无纺制品 |
| MY142099A (en) * | 2005-03-17 | 2010-09-15 | Dow Global Technologies Inc | Cap liners, closures and gaskets from multi-block polymers |
| US8084537B2 (en) * | 2005-03-17 | 2011-12-27 | Dow Global Technologies Llc | Polymer blends from interpolymers of ethylene/α-olefin with improved compatibility |
| EP1661935B2 (en) † | 2005-05-12 | 2012-05-30 | Borealis Technology Oy | Transparent easy tearable film |
| JP2009501262A (ja) * | 2005-07-15 | 2009-01-15 | エクソンモービル・ケミカル・パテンツ・インク | 熱可塑性ポリマーブレンドの生成方法 |
| US7094856B1 (en) * | 2005-07-25 | 2006-08-22 | Fina Technology, Inc. | Process for producing polyolefin |
| US7473745B2 (en) * | 2005-09-02 | 2009-01-06 | Equistar Chemicals, Lp | Preparation of multimodal polyethylene |
| EP1762577A1 (en) * | 2005-09-02 | 2007-03-14 | Total Petrochemicals Research Feluy | Impact copolymer of propylene prepared in single reactor |
| AR058450A1 (es) | 2005-09-15 | 2008-02-06 | Dow Global Technologies Inc | Copolimeros de bloque de olefina cataliticos con distibucion de secuencia de bloque controlada |
| JP5584416B2 (ja) * | 2005-10-21 | 2014-09-03 | バーゼル・ポリオレフィン・ゲーエムベーハー | 射出成形及びメルトブロー用途のための高いメルトフローレートを有するポリプロピレンランダムコポリマー |
| ES2398725T3 (es) | 2006-06-14 | 2013-03-21 | Avery Dennison Corporation | Material para etiquetas orientado en la dirección longitudinal que se puede conformar y cortar con troquel y etiquetas y proceso para su preparación |
| 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 |
| US7977435B2 (en) * | 2006-07-12 | 2011-07-12 | Lin Chon-Yie | Propylene polymer compositions and processes for making the same |
| WO2008011402A1 (en) | 2006-07-17 | 2008-01-24 | Avery Dennison Corporation | Asymmetric multilayered polymeric film and label stock and label thereof |
| EP1923200A1 (en) * | 2006-11-20 | 2008-05-21 | Borealis Technology Oy | Article |
| US8075830B2 (en) * | 2006-12-15 | 2011-12-13 | Fina Technology, Inc. | Polypropylene blown film |
| US8242237B2 (en) | 2006-12-20 | 2012-08-14 | Exxonmobil Chemical Patents Inc. | Phase separator and monomer recycle for supercritical polymerization process |
| EP2295478A3 (en) * | 2007-05-22 | 2011-09-07 | Borealis Technology Oy | Polypropylene copolymer |
| WO2008150572A1 (en) * | 2007-06-04 | 2008-12-11 | Exxonmobil Chemical Patents Inc. | Super-solution homogeneous propylene polymerization |
| US8318875B2 (en) * | 2008-01-18 | 2012-11-27 | Exxonmobil Chemical Patents Inc. | Super-solution homogeneous propylene polymerization and polypropylenes made therefrom |
| US8399725B2 (en) * | 2008-06-20 | 2013-03-19 | Exxonmobil Chemical Patents Inc. | Functionalized high vinyl terminated propylene based oligomers |
| US8283419B2 (en) * | 2008-06-20 | 2012-10-09 | Exxonmobil Chemical Patents Inc. | Olefin functionalization by metathesis reaction |
| US8372930B2 (en) | 2008-06-20 | 2013-02-12 | Exxonmobil Chemical Patents Inc. | High vinyl terminated propylene based oligomers |
| US8802797B2 (en) | 2008-06-20 | 2014-08-12 | Exxonmobil Chemical Patents Inc. | Vinyl-terminated macromonomer oligomerization |
| US8283428B2 (en) * | 2008-06-20 | 2012-10-09 | Exxonmobil Chemical Patents Inc. | Polymacromonomer and process for production thereof |
| US8278391B2 (en) | 2010-06-17 | 2012-10-02 | Fina Technology, Inc. | Polypropylene compositions for oriented films |
| ES2527333T5 (es) | 2011-02-14 | 2021-08-02 | Borealis Ag | Copolímero de propileno sellador |
| US9676532B2 (en) | 2012-08-15 | 2017-06-13 | Avery Dennison Corporation | Packaging reclosure label for high alcohol content products |
| CA2951030C (en) | 2014-06-02 | 2023-03-28 | Christopher J. Blackwell | Films with enhanced scuff resistance, clarity, and conformability |
| JP6725496B2 (ja) * | 2015-03-31 | 2020-07-22 | 株式会社プライムポリマー | ポリプロピレン樹脂組成物及びその製造方法、二軸延伸フィルム及びその製造方法、並びにフィルムコンデンサ用キャパシタフィルム |
| RU2723242C2 (ru) | 2015-12-11 | 2020-06-09 | Базелл Полиолефин Италия С.Р.Л. | Сополимеры пропиленовые |
| EP3487928A1 (en) * | 2016-07-25 | 2019-05-29 | ExxonMobil Chemical Patents Inc. | Bimodal polypropylene compositions and method of making same |
| CN107778391A (zh) * | 2016-08-29 | 2018-03-09 | 中国石油化工股份有限公司 | 一种负载型铬钨双金属催化剂的制备方法和应用 |
Family Cites Families (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3865903A (en) | 1973-04-16 | 1975-02-11 | Mobil Oil Corp | Heat sealable isotactic polypropylene and 1,3 pentadiene polymer |
| DE3750776T2 (de) | 1987-09-11 | 1995-04-27 | Fina Technology | Katalysatorsystem für Polyolefinproduktion mit breiter Molekulargewichtsverteilung. |
| IT1227893B (it) | 1988-12-14 | 1991-05-14 | Himont Inc Centerville Road Ne | Composizioni polipropileniche aventi buona trasparenza e migliorata resistenza all'urto |
| DE3921358A1 (de) | 1989-06-29 | 1991-01-10 | Hoechst Ag | Biaxial orientierte polypropylenfolie mit hoher mechanischer festigkeit |
| JP2894823B2 (ja) | 1989-12-06 | 1999-05-24 | 三井化学株式会社 | 耐放射線ポリプロピレン樹脂組成物及び耐放射線成形物の製造方法 |
| DE3942363A1 (de) | 1989-12-21 | 1991-06-27 | Hoechst Ag | Verfahren zur herstellung einer polypropylen-formmasse |
| US5280074A (en) | 1989-12-21 | 1994-01-18 | Hoechst Ag | Process for the preparation of a polypropylene molding composition |
| DE4015254A1 (de) | 1990-05-12 | 1991-11-14 | Hoechst Ag | Verfahren zur herstellung eines polyolefins |
| CA2048296C (en) | 1990-08-13 | 2002-09-24 | Henry G. Schirmer | Blends of polypropylene and ethylene copolymer and films made from the blend |
| EP0485823B1 (de) | 1990-11-12 | 1995-03-08 | Hoechst Aktiengesellschaft | 2-Substituierte Bisindenylmetallocene, Verfahren zu ihrer Herstellung und ihre Verwendung als Katalysatoren bei der Olefinpolymerisation |
| US5218052A (en) | 1991-02-04 | 1993-06-08 | Amoco Corporation | Olefin polymerization and copolymerization process |
| ES2155492T3 (es) | 1991-05-27 | 2001-05-16 | Basell Polyolefine Gmbh | Procedimiento para la obtencion de poliolefinas con una amplia distribucion de pesos moleculares. |
| EP0516019B1 (de) | 1991-05-27 | 1995-12-27 | Hoechst Aktiengesellschaft | Verfahren zur Herstellung von syndiotaktischen Polyolefinen mit breiter Molmassenverteilung |
| JP3402473B2 (ja) | 1991-08-20 | 2003-05-06 | 日本ポリケム株式会社 | オレフィン重合用触媒 |
| EP0538749B1 (en) | 1991-10-21 | 1995-01-11 | Mitsubishi Petrochemical Co., Ltd. | Propylene copolymer composition |
| EP0588208A3 (en) | 1992-09-12 | 1994-07-06 | Hoechst Ag | Polyolefin moulding composition with broad melt range, process and use therefore |
| WO1994028219A1 (en) * | 1993-05-25 | 1994-12-08 | Exxon Chemical Patents Inc. | Novel polyolefin fibers and their fabrics |
| DE4333128A1 (de) | 1993-09-29 | 1995-03-30 | Hoechst Ag | Verfahren zur Herstellung von Polyolefinen |
| EP0668157B1 (de) | 1994-02-21 | 2003-05-21 | Basell Polyolefine GmbH | Siegelbare polyolefinische Mehrschichtfolie, Verfahren zu ihrer Herstellung und ihre Verwendung |
| DE69506821T2 (de) | 1994-04-11 | 1999-06-10 | Mitsui Chemicals, Inc., Tokio/Tokyo | Verfahren zur herstellung einer propylen-polymerzusammensetzung und propylen-polymerzusammensetzung |
| CA2157399C (en) | 1994-04-11 | 2003-04-08 | Takashi Ueda | Process for preparing propylene polymer composition and propylene polymer composition |
| EP0691366B1 (en) | 1994-07-08 | 1999-03-10 | Tokuyama Corporation | Stretched polypropylene film |
| US5539056A (en) | 1995-01-31 | 1996-07-23 | Exxon Chemical Patents Inc. | Thermoplastic elastomers |
| US5741563A (en) * | 1995-09-18 | 1998-04-21 | Exxon Chemical Patents Inc. | Shrink films from propylene polymers |
| US5786291A (en) | 1996-02-23 | 1998-07-28 | Exxon Chemical Patents, Inc. | Engineered catalyst systems and methods for their production and use |
| CA2262468A1 (en) | 1996-09-04 | 1998-03-12 | Exxon Chemical Patents, Inc. | Improved propylene polymers for oriented films |
| US6342564B1 (en) | 1997-06-24 | 2002-01-29 | Borealis Technology Oy | Heterophasic propylene copolymer and process for its preparation |
| US6090325A (en) | 1997-09-24 | 2000-07-18 | Fina Technology, Inc. | Biaxially-oriented metallocene-based polypropylene films |
| HK1039495B (zh) | 1998-05-13 | 2004-10-08 | 埃克森美孚化学专利公司 | 丙烯均聚物及其制备方法 |
-
2001
- 2001-03-06 US US09/800,239 patent/US6576306B2/en not_active Expired - Lifetime
-
2002
- 2002-01-28 MX MXPA03008012A patent/MXPA03008012A/es unknown
- 2002-01-28 CA CA002438163A patent/CA2438163A1/en not_active Abandoned
- 2002-01-28 CN CNA028060873A patent/CN1498231A/zh active Pending
- 2002-01-28 AU AU2002243700A patent/AU2002243700A1/en not_active Abandoned
- 2002-01-28 WO PCT/US2002/002469 patent/WO2002070570A2/en not_active Ceased
- 2002-01-28 JP JP2002570607A patent/JP2004528420A/ja active Pending
- 2002-01-28 BR BR0207885-6A patent/BR0207885A/pt not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| US20010039314A1 (en) | 2001-11-08 |
| JP2004528420A (ja) | 2004-09-16 |
| AU2002243700A1 (en) | 2002-09-19 |
| CN1498231A (zh) | 2004-05-19 |
| US6576306B2 (en) | 2003-06-10 |
| WO2002070570A3 (en) | 2002-12-19 |
| BR0207885A (pt) | 2004-07-27 |
| WO2002070570A2 (en) | 2002-09-12 |
| MXPA03008012A (es) | 2004-04-02 |
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| Date | Code | Title | Description |
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