JP3425794B2 - 支持された触媒システムとその調製、及びオレフィンの重合に対するその利用 - Google Patents
支持された触媒システムとその調製、及びオレフィンの重合に対するその利用Info
- Publication number
- JP3425794B2 JP3425794B2 JP01652694A JP1652694A JP3425794B2 JP 3425794 B2 JP3425794 B2 JP 3425794B2 JP 01652694 A JP01652694 A JP 01652694A JP 1652694 A JP1652694 A JP 1652694A JP 3425794 B2 JP3425794 B2 JP 3425794B2
- Authority
- JP
- Japan
- Prior art keywords
- zirconium dichloride
- dimethylsilylbis
- cyclopentadienyl
- fluorenyl
- dichloride
- 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.)
- Expired - Fee Related
Links
- 239000003054 catalyst Substances 0.000 title claims description 92
- 238000006116 polymerization reaction Methods 0.000 title claims description 54
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 title claims description 12
- 238000002360 preparation method Methods 0.000 title claims description 6
- 150000001336 alkenes Chemical class 0.000 title description 5
- -1 butylcyclopentadienyl Chemical group 0.000 claims description 86
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 75
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Natural products CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 44
- VPGLGRNSAYHXPY-UHFFFAOYSA-L zirconium(2+);dichloride Chemical compound Cl[Zr]Cl VPGLGRNSAYHXPY-UHFFFAOYSA-L 0.000 claims description 35
- 239000000725 suspension Substances 0.000 claims description 31
- 238000000034 method Methods 0.000 claims description 24
- 239000000463 material Substances 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 15
- 239000000843 powder Substances 0.000 claims description 14
- 239000007787 solid Substances 0.000 claims description 12
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 claims description 10
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 9
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 claims description 8
- 229920000098 polyolefin Polymers 0.000 claims description 8
- 239000000126 substance Substances 0.000 claims description 8
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
- 229910052726 zirconium Inorganic materials 0.000 claims description 7
- 239000002904 solvent Substances 0.000 claims description 6
- 238000003756 stirring Methods 0.000 claims description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 5
- 239000000741 silica gel Substances 0.000 claims description 5
- 229910002027 silica gel Inorganic materials 0.000 claims description 5
- 239000002283 diesel fuel Substances 0.000 claims description 4
- 230000008569 process Effects 0.000 claims description 4
- 150000003254 radicals Chemical class 0.000 claims description 4
- AGKZDUBMFACJPR-UHFFFAOYSA-L C12=CC=CC=C2C2=CC=CC=C2C1[Zr](Cl)(Cl)(=C(C)C)C1C=CC=C1 Chemical compound C12=CC=CC=C2C2=CC=CC=C2C1[Zr](Cl)(Cl)(=C(C)C)C1C=CC=C1 AGKZDUBMFACJPR-UHFFFAOYSA-L 0.000 claims description 3
- OIFOECOMQYQXLY-UHFFFAOYSA-L CC(C)[Zr](Cl)(Cl)(C1C=CC(C)=C1)C1C=CC2=CC=CC=C12 Chemical compound CC(C)[Zr](Cl)(Cl)(C1C=CC(C)=C1)C1C=CC2=CC=CC=C12 OIFOECOMQYQXLY-UHFFFAOYSA-L 0.000 claims description 3
- YXPOWZMEGBMKQO-UHFFFAOYSA-L CC(C)[Zr](Cl)(Cl)(C1C=CC=C1)C1C=CC2=CC=CC=C12 Chemical compound CC(C)[Zr](Cl)(Cl)(C1C=CC=C1)C1C=CC2=CC=CC=C12 YXPOWZMEGBMKQO-UHFFFAOYSA-L 0.000 claims description 3
- VWOTWOPAYZNLIU-UHFFFAOYSA-L C[SiH]C.Cl[Zr](Cl)(C1C=CC=C1)C1C=CC=C1 Chemical compound C[SiH]C.Cl[Zr](Cl)(C1C=CC=C1)C1C=CC=C1 VWOTWOPAYZNLIU-UHFFFAOYSA-L 0.000 claims description 3
- SVHPGKHHBXQFLQ-UHFFFAOYSA-L Cl[Zr](Cl)(C1C=CC=C1)(C1c2ccccc2-c2ccccc12)=C(c1ccccc1)c1ccccc1 Chemical compound Cl[Zr](Cl)(C1C=CC=C1)(C1c2ccccc2-c2ccccc12)=C(c1ccccc1)c1ccccc1 SVHPGKHHBXQFLQ-UHFFFAOYSA-L 0.000 claims description 3
- IKMQPGOYCLXVSL-UHFFFAOYSA-L [Cl-].[Cl-].C1(C=CC=C1)[Zr+2]C1C2=CC=CC=C2C=2C=CC=CC1=2 Chemical compound [Cl-].[Cl-].C1(C=CC=C1)[Zr+2]C1C2=CC=CC=C2C=2C=CC=CC1=2 IKMQPGOYCLXVSL-UHFFFAOYSA-L 0.000 claims description 3
- FJMJPZLXUXRLLD-UHFFFAOYSA-L [Cl-].[Cl-].C1=CC2=CC=CC=C2C1[Zr+2]([SiH](C)C)C1C2=CC=CC=C2C=C1 Chemical compound [Cl-].[Cl-].C1=CC2=CC=CC=C2C1[Zr+2]([SiH](C)C)C1C2=CC=CC=C2C=C1 FJMJPZLXUXRLLD-UHFFFAOYSA-L 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 claims description 3
- ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 claims description 3
- QMBQEXOLIRBNPN-UHFFFAOYSA-L zirconocene dichloride Chemical compound [Cl-].[Cl-].[Zr+4].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 QMBQEXOLIRBNPN-UHFFFAOYSA-L 0.000 claims description 3
- OSIHYASBAJHECK-UHFFFAOYSA-L 1,2-dimethylcyclopenta-1,3-diene;zirconium(4+);dichloride Chemical compound [Cl-].[Cl-].[Zr+4].CC1=C(C)[C-]=CC1.CC1=C(C)[C-]=CC1 OSIHYASBAJHECK-UHFFFAOYSA-L 0.000 claims description 2
- RDWHKWXYJQUZNS-UHFFFAOYSA-N 4-propan-2-yl-1,3-thiazole-2-carboxylic acid Chemical compound CC(C)C1=CSC(C(O)=O)=N1 RDWHKWXYJQUZNS-UHFFFAOYSA-N 0.000 claims description 2
- XBBHYFLWNUTSGU-UHFFFAOYSA-L CC(C)=[Hf](Cl)(Cl)(C1C=CC=C1)C1c2ccccc2-c2ccccc12 Chemical compound CC(C)=[Hf](Cl)(Cl)(C1C=CC=C1)C1c2ccccc2-c2ccccc12 XBBHYFLWNUTSGU-UHFFFAOYSA-L 0.000 claims description 2
- OXLXAPYJCPFBFT-UHFFFAOYSA-L CC1=CC(C)(C=C1)[Zr](Cl)(Cl)C1(C)C=CC(C)=C1 Chemical compound CC1=CC(C)(C=C1)[Zr](Cl)(Cl)C1(C)C=CC(C)=C1 OXLXAPYJCPFBFT-UHFFFAOYSA-L 0.000 claims description 2
- DTDVAAXCMOLOAZ-UHFFFAOYSA-L C[SiH](C)[Hf](Cl)(Cl)(C1C=CC=C1)C1c2ccccc2-c2ccccc12 Chemical compound C[SiH](C)[Hf](Cl)(Cl)(C1C=CC=C1)C1c2ccccc2-c2ccccc12 DTDVAAXCMOLOAZ-UHFFFAOYSA-L 0.000 claims description 2
- CTBFXDVGDCMIQR-UHFFFAOYSA-L C[SiH](C)[Zr](Cl)(Cl)(C1C=CC=C1)C1C=Cc2ccccc12 Chemical compound C[SiH](C)[Zr](Cl)(Cl)(C1C=CC=C1)C1C=Cc2ccccc12 CTBFXDVGDCMIQR-UHFFFAOYSA-L 0.000 claims description 2
- MPJLHVOQWLKMRN-UHFFFAOYSA-L C[SiH](C)[Zr](Cl)(Cl)(C1C=CC=C1)C1c2ccccc2-c2ccccc12 Chemical compound C[SiH](C)[Zr](Cl)(Cl)(C1C=CC=C1)C1c2ccccc2-c2ccccc12 MPJLHVOQWLKMRN-UHFFFAOYSA-L 0.000 claims description 2
- NKMKIZXPSDBKLH-UHFFFAOYSA-L C[SiH]C.CC1=CC(C(C)=C1)[Zr](Cl)(Cl)C1C=C(C)C=C1C Chemical compound C[SiH]C.CC1=CC(C(C)=C1)[Zr](Cl)(Cl)C1C=C(C)C=C1C NKMKIZXPSDBKLH-UHFFFAOYSA-L 0.000 claims description 2
- WCQGHWSRJKSCSK-UHFFFAOYSA-L [Cl-].[Cl-].C12=CC=CC=C2C2=CC=CC=C2C1[Zr+2]([SiH](C)C)C1C2=CC=CC=C2C=C1 Chemical compound [Cl-].[Cl-].C12=CC=CC=C2C2=CC=CC=C2C1[Zr+2]([SiH](C)C)C1C2=CC=CC=C2C=C1 WCQGHWSRJKSCSK-UHFFFAOYSA-L 0.000 claims description 2
- DPXFROCZZRXAGW-UHFFFAOYSA-L [Cl-].[Cl-].C1=CC2=CC=CC=C2C1[Zr+2]([GeH](C)C)C1C2=CC=CC=C2C=C1 Chemical compound [Cl-].[Cl-].C1=CC2=CC=CC=C2C1[Zr+2]([GeH](C)C)C1C2=CC=CC=C2C=C1 DPXFROCZZRXAGW-UHFFFAOYSA-L 0.000 claims description 2
- RLEZACANRPOGPQ-UHFFFAOYSA-L [Cl-].[Cl-].C1CC2CC=CC=C2C1[Zr+2]([SiH](C)C)C1C2=CC=CCC2CC1 Chemical compound [Cl-].[Cl-].C1CC2CC=CC=C2C1[Zr+2]([SiH](C)C)C1C2=CC=CCC2CC1 RLEZACANRPOGPQ-UHFFFAOYSA-L 0.000 claims description 2
- UKIIISQOHOTQGE-UHFFFAOYSA-L [Cl-].[Cl-].CC(C)[Zr++](C1C=Cc2ccccc12)C1c2ccccc2-c2ccccc12 Chemical compound [Cl-].[Cl-].CC(C)[Zr++](C1C=Cc2ccccc12)C1c2ccccc2-c2ccccc12 UKIIISQOHOTQGE-UHFFFAOYSA-L 0.000 claims description 2
- SPEWZEXMYFWEDM-UHFFFAOYSA-L [Cl-].[Cl-].CC=C.C1=CC2=CC=CC=C2C1[Zr+2]C1C2=CC=CC=C2C=C1 Chemical compound [Cl-].[Cl-].CC=C.C1=CC2=CC=CC=C2C1[Zr+2]C1C2=CC=CC=C2C=C1 SPEWZEXMYFWEDM-UHFFFAOYSA-L 0.000 claims description 2
- 150000005840 aryl radicals Chemical class 0.000 claims description 2
- 239000003426 co-catalyst Substances 0.000 claims description 2
- 125000004122 cyclic group Chemical group 0.000 claims description 2
- MIILMDFFARLWKZ-UHFFFAOYSA-L dichlorozirconium;1,2,3,4,5-pentamethylcyclopentane Chemical compound [Cl-].[Cl-].CC1=C(C)C(C)=C(C)C1(C)[Zr+2]C1(C)C(C)=C(C)C(C)=C1C MIILMDFFARLWKZ-UHFFFAOYSA-L 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- AQYCWSHDYILNJO-UHFFFAOYSA-N methyl 6-methyl-3-oxo-4h-1,4-benzoxazine-8-carboxylate Chemical compound N1C(=O)COC2=C1C=C(C)C=C2C(=O)OC AQYCWSHDYILNJO-UHFFFAOYSA-N 0.000 claims description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 239000000047 product Substances 0.000 claims description 2
- 239000006228 supernatant Substances 0.000 claims description 2
- 230000001678 irradiating effect Effects 0.000 claims 4
- 230000002194 synthesizing effect Effects 0.000 claims 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
- XFNIQDLAPZZUMH-UHFFFAOYSA-N 2-methyl-4,6-di(propan-2-yl)-1h-indene Chemical compound CC(C)C1=CC(C(C)C)=CC2=C1C=C(C)C2 XFNIQDLAPZZUMH-UHFFFAOYSA-N 0.000 claims 1
- FKOZSEFAYSVZLJ-UHFFFAOYSA-L C[SiH]C.CC1=CC(C=C1)[Zr](Cl)(Cl)C1C=CC(C)=C1 Chemical compound C[SiH]C.CC1=CC(C=C1)[Zr](Cl)(Cl)C1C=CC(C)=C1 FKOZSEFAYSVZLJ-UHFFFAOYSA-L 0.000 claims 1
- SCVXORFLOXDESF-UHFFFAOYSA-L Cl[Hf](Cl)(C1C=CC=C1)(C1c2ccccc2-c2ccccc12)=C(c1ccccc1)c1ccccc1 Chemical compound Cl[Hf](Cl)(C1C=CC=C1)(C1c2ccccc2-c2ccccc12)=C(c1ccccc1)c1ccccc1 SCVXORFLOXDESF-UHFFFAOYSA-L 0.000 claims 1
- OAGXCGFJNYFZDE-UHFFFAOYSA-L [Cl-].[Cl-].C(CC)C1(C=CC=C1)[Zr+2]C1(C=CC=C1)CCC Chemical compound [Cl-].[Cl-].C(CC)C1(C=CC=C1)[Zr+2]C1(C=CC=C1)CCC OAGXCGFJNYFZDE-UHFFFAOYSA-L 0.000 claims 1
- 238000004140 cleaning Methods 0.000 claims 1
- LOKCKYUBKHNUCV-UHFFFAOYSA-L dichlorozirconium;methylcyclopentane Chemical compound Cl[Zr]Cl.C[C]1[CH][CH][CH][CH]1.C[C]1[CH][CH][CH][CH]1 LOKCKYUBKHNUCV-UHFFFAOYSA-L 0.000 claims 1
- 125000003944 tolyl group Chemical group 0.000 claims 1
- 239000004743 Polypropylene Substances 0.000 description 19
- 229920001155 polypropylene Polymers 0.000 description 19
- 238000006243 chemical reaction Methods 0.000 description 13
- 238000001816 cooling Methods 0.000 description 10
- 230000000694 effects Effects 0.000 description 10
- 238000002474 experimental method Methods 0.000 description 10
- 239000000178 monomer Substances 0.000 description 10
- 229920000642 polymer Polymers 0.000 description 10
- 239000002245 particle Substances 0.000 description 9
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 8
- 229920001577 copolymer Polymers 0.000 description 8
- 239000005977 Ethylene Substances 0.000 description 7
- 229910004298 SiO 2 Inorganic materials 0.000 description 6
- 230000003197 catalytic effect Effects 0.000 description 6
- 230000008859 change Effects 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 229930195733 hydrocarbon Natural products 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 5
- 239000004215 Carbon black (E152) Substances 0.000 description 5
- 125000004429 atom Chemical group 0.000 description 5
- 239000000706 filtrate Substances 0.000 description 5
- 239000007789 gas Substances 0.000 description 5
- 239000011261 inert gas Substances 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- 239000012442 inert solvent Substances 0.000 description 4
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 4
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 3
- 150000001925 cycloalkenes Chemical class 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 229910052735 hafnium Inorganic materials 0.000 description 3
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 239000012968 metallocene catalyst Substances 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 description 2
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 description 2
- GOKFSCDYLXSQRU-UHFFFAOYSA-L CC(C)[Zr](Cl)(Cl)(C1C=CC=C1)C1C2=CC=CC=C2C2=C1C=CC=C2 Chemical compound CC(C)[Zr](Cl)(Cl)(C1C=CC=C1)C1C2=CC=CC=C2C2=C1C=CC=C2 GOKFSCDYLXSQRU-UHFFFAOYSA-L 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 125000002015 acyclic group Chemical group 0.000 description 2
- 125000005234 alkyl aluminium group Chemical group 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- ZMMRKRFMSDTOLV-UHFFFAOYSA-N cyclopenta-1,3-diene zirconium Chemical compound [Zr].C1C=CC=C1.C1C=CC=C1 ZMMRKRFMSDTOLV-UHFFFAOYSA-N 0.000 description 2
- 229910052732 germanium Inorganic materials 0.000 description 2
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- CPOFMOWDMVWCLF-UHFFFAOYSA-N methyl(oxo)alumane Chemical compound C[Al]=O CPOFMOWDMVWCLF-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 1
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 1
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 1
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 1
- 125000000041 C6-C10 aryl group Chemical group 0.000 description 1
- ODBIJJPVHKLQGB-UHFFFAOYSA-N C[SiH](C)[Zr](C1C=CC=C1)(C1C=CC=C1)C1C2=CC=CC=C2C=C1.Cl.Cl Chemical compound C[SiH](C)[Zr](C1C=CC=C1)(C1C=CC=C1)C1C2=CC=CC=C2C=C1.Cl.Cl ODBIJJPVHKLQGB-UHFFFAOYSA-N 0.000 description 1
- SNQFNJBZYZBXGD-UHFFFAOYSA-L Cl[Hf](Cl)C1C=CC=C1 Chemical compound Cl[Hf](Cl)C1C=CC=C1 SNQFNJBZYZBXGD-UHFFFAOYSA-L 0.000 description 1
- XJONFIGVOQMBIP-UHFFFAOYSA-L Cl[Zr](Cl)C1C=CC=C1 Chemical compound Cl[Zr](Cl)C1C=CC=C1 XJONFIGVOQMBIP-UHFFFAOYSA-L 0.000 description 1
- NZDLIIBVQQCHBI-UHFFFAOYSA-L Cl[Zr]Cl.CC1=C[CH]C=C1 Chemical compound Cl[Zr]Cl.CC1=C[CH]C=C1 NZDLIIBVQQCHBI-UHFFFAOYSA-L 0.000 description 1
- YZCKVEUIGOORGS-IGMARMGPSA-N Protium Chemical compound [1H] YZCKVEUIGOORGS-IGMARMGPSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- DHOIFLAXQKMNNF-UHFFFAOYSA-L [Cl-].[Cl-].C1=CC2=CC=CC=C2C1[Zr+2](C1C2=CC=CC=C2C=C1)[SiH](C=1C=CC=CC=1)C1=CC=CC=C1 Chemical compound [Cl-].[Cl-].C1=CC2=CC=CC=C2C1[Zr+2](C1C2=CC=CC=C2C=C1)[SiH](C=1C=CC=CC=1)C1=CC=CC=C1 DHOIFLAXQKMNNF-UHFFFAOYSA-L 0.000 description 1
- QSZGOMRHQRFORD-UHFFFAOYSA-L [Cl-].[Cl-].C=C.C1=CC2=CC=CC=C2C1[Zr+2]C1C2=CC=CC=C2C=C1 Chemical compound [Cl-].[Cl-].C=C.C1=CC2=CC=CC=C2C1[Zr+2]C1C2=CC=CC=C2C=C1 QSZGOMRHQRFORD-UHFFFAOYSA-L 0.000 description 1
- AWXKEFJIQBQSSC-UHFFFAOYSA-L [Cl-].[Cl-].CC1=CC(C)([Zr++]C2(C)C=C(C)C(C)=C2)C=C1C Chemical compound [Cl-].[Cl-].CC1=CC(C)([Zr++]C2(C)C=C(C)C(C)=C2)C=C1C AWXKEFJIQBQSSC-UHFFFAOYSA-L 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 239000012300 argon atmosphere Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- SFFFIHNOEGSAIH-UHFFFAOYSA-N bicyclo[2.2.1]hept-2-ene;ethene Chemical group C=C.C1C2CCC1C=C2 SFFFIHNOEGSAIH-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- KZUKCLOWAMFDDB-UHFFFAOYSA-L butylcyclopentane;dichlorozirconium Chemical compound Cl[Zr]Cl.CCCC[C]1[CH][CH][CH][CH]1.CCCC[C]1[CH][CH][CH][CH]1 KZUKCLOWAMFDDB-UHFFFAOYSA-L 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 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
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- 238000010907 mechanical stirring Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 125000002950 monocyclic group Chemical group 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
- 229910052758 niobium Inorganic materials 0.000 description 1
- 239000010955 niobium Substances 0.000 description 1
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 125000000538 pentafluorophenyl group Chemical group FC1=C(F)C(F)=C(*)C(F)=C1F 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- XOJVVFBFDXDTEG-UHFFFAOYSA-N pristane Chemical compound CC(C)CCCC(C)CCCC(C)CCCC(C)C XOJVVFBFDXDTEG-UHFFFAOYSA-N 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 230000036962 time dependent Effects 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- SQBBHCOIQXKPHL-UHFFFAOYSA-N tributylalumane Chemical compound CCCC[Al](CCCC)CCCC SQBBHCOIQXKPHL-UHFFFAOYSA-N 0.000 description 1
- MCULRUJILOGHCJ-UHFFFAOYSA-N triisobutylaluminium Chemical compound CC(C)C[Al](CC(C)C)CC(C)C MCULRUJILOGHCJ-UHFFFAOYSA-N 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
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- 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
- C08F4/00—Polymerisation catalysts
- 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
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
- C08F4/65912—Component covered by group C08F4/64 containing a transition metal-carbon bond in combination with an organoaluminium compound
-
- 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
- C08F4/00—Polymerisation catalysts
- 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
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
- C08F4/65916—Component covered by group C08F4/64 containing a transition metal-carbon bond supported on a carrier, e.g. silica, MgCl2, polymer
-
- 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
- C08F4/00—Polymerisation catalysts
- 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
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
- C08F4/6592—Component covered by group C08F4/64 containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring
- C08F4/65922—Component covered by group C08F4/64 containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring containing at least two cyclopentadienyl rings, fused or not
-
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S502/00—Catalyst, solid sorbent, or support therefor: product or process of making
- Y10S502/522—Radiant or wave energy activated
-
- 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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S526/943—Polymerization with metallocene catalysts
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)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4304286:4 | 1993-02-12 | ||
| DE4304286 | 1993-02-12 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH072920A JPH072920A (ja) | 1995-01-06 |
| JP3425794B2 true JP3425794B2 (ja) | 2003-07-14 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP01652694A Expired - Fee Related JP3425794B2 (ja) | 1993-02-12 | 1994-02-10 | 支持された触媒システムとその調製、及びオレフィンの重合に対するその利用 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US5719095A (index.php) |
| EP (1) | EP0615981B1 (index.php) |
| JP (1) | JP3425794B2 (index.php) |
| KR (1) | KR100312665B1 (index.php) |
| CN (1) | CN1053673C (index.php) |
| DE (1) | DE59405876D1 (index.php) |
| TW (1) | TW298593B (index.php) |
Families Citing this family (71)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6143686A (en) * | 1994-08-03 | 2000-11-07 | Exxon Chemical Patents, Inc. | Supported ionic catalyst compositions |
| US6043180A (en) * | 1994-11-17 | 2000-03-28 | The Dow Chemical Company | Supported catalyst component, supported catalyst, their preparation, and addition polymerization process |
| US6506866B2 (en) * | 1994-11-17 | 2003-01-14 | Dow Global Technologies Inc. | Ethylene copolymer compositions |
| ATE229987T1 (de) * | 1994-11-17 | 2003-01-15 | Dow Chemical Co | Trägerkatalysatorkomponent, trägerkatalysator, ihre herstellung und additionspolymerisationsverfahren |
| DE69710838T2 (de) * | 1996-04-22 | 2002-10-31 | Japan Polyolefins Co. Ltd., Tokio/Tokyo | Katalysator zur polyolefinherstellung und polyolefinherstellungsverfahren |
| JPH10120716A (ja) * | 1996-08-27 | 1998-05-12 | Mitsui Chem Inc | 予備重合固体状触媒、その調製方法およびオレフィンの不均一系重合方法 |
| US5968864A (en) * | 1996-12-20 | 1999-10-19 | Fina Technology, Inc. | Catalyst efficiency for supported metallocene catalyst |
| US6245868B1 (en) | 1998-05-29 | 2001-06-12 | Univation Technologies | Catalyst delivery method, a catalyst feeder and their use in a polymerization process |
| US6562918B1 (en) * | 1999-02-04 | 2003-05-13 | Idemitsu Petrochemical Co., Ltd. | Olefin polymerization catalyst, method for producing the same and method for producing olefinic polymer |
| ES2394304T3 (es) | 2002-10-15 | 2013-01-30 | Exxonmobil Chemical Patents, Inc. | Sistema de múltiples catalizadores para la polimerización de olefinas y polímeros producidos a partir de éstos |
| US7223822B2 (en) | 2002-10-15 | 2007-05-29 | Exxonmobil Chemical Patents Inc. | Multiple catalyst and reactor system for olefin polymerization and polymers produced therefrom |
| AR048273A1 (es) | 2004-03-17 | 2006-04-12 | Dow Global Technologies Inc | Composicion catalizadora que comprende un agente de enlace para la formacion de copolimeros de etileno |
| SG151301A1 (en) | 2004-03-17 | 2009-04-30 | Dow Global Technologies Inc | Catalyst composition comprising shuttling agent for ethylene multi- block copolymer formation |
| MXPA06010481A (es) | 2004-03-17 | 2006-12-19 | Dow Global Technologies Inc | Composicion catalizadora que comprende agente de enlace para la formacion de copolimeros de multiples bloques de olefina superior. |
| WO2005109099A1 (ja) * | 2004-05-07 | 2005-11-17 | Hitachi Chemical Dupont Microsystems Ltd. | ポジ型感光性樹脂組成物、パターンの製造方法及び電子部品 |
| EP1763542B1 (en) | 2004-06-16 | 2011-04-06 | Dow Global Technologies Inc. | Technique for selecting polymerization modifiers |
| US20080051537A1 (en) | 2004-08-09 | 2008-02-28 | Carnahan Edmund M | Supported Bis(Hydroxylarylaryloxy) Catalysts For Manufacture Of Polymers |
| US7399874B2 (en) | 2004-10-29 | 2008-07-15 | Exxonmobil Chemical Patents Inc. | Catalyst compound containing divalent tridentate ligand |
| JP5225686B2 (ja) | 2004-12-21 | 2013-07-03 | ダウ グローバル テクノロジーズ エルエルシー | ポリプロピレンをベースとした接着剤組成物 |
| JP2008533276A (ja) | 2005-03-17 | 2008-08-21 | ダウ グローバル テクノロジーズ インコーポレイティド | タクチック／アタクチックマルチブロックコポリマー形成用の可逆的移動剤を含む触媒組成物 |
| CN101142245B (zh) | 2005-03-17 | 2012-08-08 | 陶氏环球技术有限责任公司 | 用于形成立体无规多嵌段共聚物的包含梭移剂的催化剂组合物 |
| US9410009B2 (en) | 2005-03-17 | 2016-08-09 | Dow Global Technologies Llc | Catalyst composition comprising shuttling agent for tactic/ atactic multi-block copolymer formation |
| EP1721913A1 (en) * | 2005-05-09 | 2006-11-15 | Total Petrochemicals Research Feluy | Microwave-promoted creation of catalytic species |
| CA2622599A1 (en) | 2005-09-15 | 2007-03-29 | Dow Global Technolgies Inc. | Control of polymer architecture and molecular weight distribution via multi-centered shuttling agent |
| AR058449A1 (es) | 2005-09-15 | 2008-02-06 | Dow Global Technologies Inc | Copolimeros de bloque de olefina cataliticos via un agente de transferencia polimerizable |
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| EP1803747A1 (en) | 2005-12-30 | 2007-07-04 | Borealis Technology Oy | Surface-modified polymerization catalysts for the preparation of low-gel polyolefin films |
| WO2007136497A2 (en) | 2006-05-17 | 2007-11-29 | Dow Global Technologies Inc. | High temperature solution polymerization process |
| US7879748B2 (en) * | 2006-08-09 | 2011-02-01 | Umicore Ag & Co. Kg | Method for producing a catalyst and the catalyst made therefrom |
| CN101711258B (zh) | 2007-03-07 | 2012-07-04 | 陶氏环球技术有限责任公司 | 系连负载型过渡金属络合物 |
| ITMI20070877A1 (it) | 2007-05-02 | 2008-11-03 | Dow Global Technologies Inc | Processo per la produzione di copolimeri a blocchi multipli con l'utilizzo di solventi polari |
| ITMI20070878A1 (it) | 2007-05-02 | 2008-11-03 | Dow Global Technologies Inc | Processo per la polimerizzazine di polimeri tattici con l'uso di catalizzatori chirali |
| TW200932762A (en) | 2007-10-22 | 2009-08-01 | Univation Tech Llc | Polyethylene compositions having improved properties |
| CN101918463B (zh) | 2007-11-19 | 2012-09-05 | 陶氏环球技术有限责任公司 | 长链支化丙烯-α-烯烃共聚物 |
| EP2358767B1 (en) | 2008-12-18 | 2013-02-20 | Univation Technologies, LLC | Method for seed bed treatment for a polymerization reaction |
| US8592615B2 (en) | 2009-03-06 | 2013-11-26 | Dow Global Technologies, Llc | Catalysts, processes for making catalysts, processes for making polyolefin compositions, and polyolefin compositions |
| CN102498133B (zh) | 2009-07-29 | 2013-10-30 | 陶氏环球技术有限责任公司 | 双头基或多头基的链穿梭剂以及它们用于制备嵌段共聚物的用途 |
| WO2011016992A2 (en) | 2009-07-29 | 2011-02-10 | Dow Global Technologies Inc. | Polymeric chain transfer/shuttling agents |
| CA2777230C (en) | 2009-10-19 | 2015-12-22 | Sasol Technology (Pty) Limited | Oligomerisation of olefinic compounds with reduced polymer formation |
| WO2011050566A1 (zh) | 2009-10-26 | 2011-05-05 | 中国石油化工股份有限公司 | 负载型非茂金属催化剂、其制备方法及其应用 |
| EP2495261B1 (en) | 2009-10-26 | 2020-08-26 | China Petroleum & Chemical Corporation | Supported non-metallocene catalyst, manufacturing method and application thereof |
| EP2500365B1 (en) | 2009-11-13 | 2020-05-06 | China Petroleum & Chemical Corporation | Supported non-metallocene catalyst and preparation method and uses thereof |
| JP5670465B2 (ja) | 2009-11-13 | 2015-02-18 | 中國石油化工股▲分▼有限公司 | 担持型非メタロセン触媒、その製造方法およびその使用 |
| RU2430116C1 (ru) | 2010-01-29 | 2011-09-27 | Закрытое Акционерное Общество "Сибур Холдинг" | Способ полимеризации и сополимеризации олефиновых олигомеров |
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| CN103228682B (zh) | 2010-11-30 | 2015-07-22 | 尤尼威蒂恩技术有限责任公司 | 用经萃取的金属羧酸盐聚合烯烃的方法 |
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| CN105121015A (zh) | 2013-01-14 | 2015-12-02 | 尤尼威蒂恩技术有限责任公司 | 制备高产率催化剂系统的方法 |
| US20150353651A1 (en) | 2013-01-30 | 2015-12-10 | Univation Technologies, Llc | Processes for making catalyst compositions having improved flow |
| US10069965B2 (en) | 2013-08-29 | 2018-09-04 | Unify Gmbh & Co. Kg | Maintaining audio communication in a congested communication channel |
| US9712666B2 (en) | 2013-08-29 | 2017-07-18 | Unify Gmbh & Co. Kg | Maintaining audio communication in a congested communication channel |
| CN106164104A (zh) | 2014-04-02 | 2016-11-23 | 尤尼威蒂恩技术有限责任公司 | 连续性组合物及其制备和使用方法 |
| US10414843B2 (en) | 2015-03-10 | 2019-09-17 | Univation Technologies, Llc | Spray dried catalyst compositions, methods for preparation and use in olefin polymerization processes |
| EP3286202B1 (en) | 2015-04-20 | 2019-03-13 | Univation Technologies, LLC | Bridged bi-aromatic ligands and transition metal compounds prepared therefrom |
| SG11201708410UA (en) | 2015-04-20 | 2017-11-29 | Univation Tech Llc | Bridged bi-aromatic ligands and olefin polymerization catalysts prepared therefrom |
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| EP3356374B1 (en) | 2015-09-30 | 2025-09-24 | Dow Global Technologies LLC | Multi- or dual-headed compositions useful for chain shuttling and process to prepare the same |
| CN109963888A (zh) | 2016-09-30 | 2019-07-02 | 陶氏环球技术有限责任公司 | 用于制备适用于链梭移的多头或双头组合物的方法 |
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| KR20210119985A (ko) | 2018-12-28 | 2021-10-06 | 다우 글로벌 테크놀로지스 엘엘씨 | 불포화 폴리올레핀을 포함하는 경화성 조성물 |
| US11999814B2 (en) | 2021-12-16 | 2024-06-04 | Chevron Phillips Chemical Company Lp | Modifications of sulfated bentonites and uses thereof in metallocene catalyst systems for olefin polymerization |
| CN115650286B (zh) * | 2022-10-24 | 2024-06-21 | 浙江大学 | 一种rGO/MXene/TiO2/Fe2C多级异质结构多孔微球吸波材料的制备方法 |
| CN117586439B (zh) * | 2024-01-17 | 2024-03-26 | 营口风光新材料股份有限公司 | 一种复合型茂金属催化剂及其制备方法与应用 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1530445A (en) * | 1976-01-09 | 1978-11-01 | British Petroleum Co | Polymerisation catalyst |
| US4564647A (en) * | 1983-11-14 | 1986-01-14 | Idemitsu Kosan Company Limited | Process for the production of polyethylene compositions |
| EP0314797B1 (en) * | 1987-04-20 | 1997-07-02 | Mitsui Petrochemical Industries, Ltd. | Olefin polymerization catalyst and process for polymerizing olefin |
| JP2538595B2 (ja) * | 1987-05-13 | 1996-09-25 | 三井石油化学工業株式会社 | オレフイン重合用固体触媒 |
| FR2659337B1 (fr) * | 1990-03-12 | 1992-06-05 | Bp Chemicals Snc | Procede de preparation d'un catalyseur a base de zirconium, de titane et/ou de vanadium supporte sur du chlorure de magnesium, et utilisation du catalyseur dans la polymerisation des olefines. |
| DE69219206T2 (de) * | 1991-05-31 | 1997-08-28 | Mitsui Petrochemical Ind | Fester Katalysatorbestandteil, Katalysator und Verfahren für Olefinpolymerisation |
| DE4121368A1 (de) * | 1991-06-28 | 1993-01-07 | Hoechst Ag | Katalysator und verfahren zur herstellung von hochmolekularen polyolefinen |
| TW337527B (en) * | 1992-01-24 | 1998-08-01 | Hoechst Ag | Catalyst for the polymerization of olefins, process for the preparation thereof, and use thereof |
| TW304963B (index.php) * | 1992-01-27 | 1997-05-11 | Hoechst Ag | |
| FI112233B (fi) * | 1992-04-01 | 2003-11-14 | Basell Polyolefine Gmbh | Katalyytti olefiinipolymerointia varten, menetelmä sen valmistamiseksi ja sen käyttö |
| EP0578838A1 (en) * | 1992-04-29 | 1994-01-19 | Hoechst Aktiengesellschaft | Olefin polymerization catalyst, process for its preparation, and its use |
| TW369545B (en) * | 1993-02-12 | 1999-09-11 | Hoechst Ag | Process for preparing cycloolefin copolymers |
-
1994
- 1994-02-04 TW TW083100946A patent/TW298593B/zh active
- 1994-02-07 DE DE59405876T patent/DE59405876D1/de not_active Expired - Fee Related
- 1994-02-07 EP EP94101797A patent/EP0615981B1/de not_active Expired - Lifetime
- 1994-02-08 CN CN94101358A patent/CN1053673C/zh not_active Expired - Fee Related
- 1994-02-10 JP JP01652694A patent/JP3425794B2/ja not_active Expired - Fee Related
- 1994-02-10 US US08/196,285 patent/US5719095A/en not_active Expired - Fee Related
- 1994-02-12 KR KR1019940002491A patent/KR100312665B1/ko not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| TW298593B (index.php) | 1997-02-21 |
| KR100312665B1 (ko) | 2001-12-28 |
| EP0615981A3 (de) | 1994-11-17 |
| EP0615981A2 (de) | 1994-09-21 |
| JPH072920A (ja) | 1995-01-06 |
| EP0615981B1 (de) | 1998-05-06 |
| DE59405876D1 (de) | 1998-06-10 |
| CN1053673C (zh) | 2000-06-21 |
| US5719095A (en) | 1998-02-17 |
| CN1096517A (zh) | 1994-12-21 |
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