JP2000504775A - 担持触媒組成物 - Google Patents
担持触媒組成物Info
- Publication number
- JP2000504775A JP2000504775A JP9529783A JP52978397A JP2000504775A JP 2000504775 A JP2000504775 A JP 2000504775A JP 9529783 A JP9529783 A JP 9529783A JP 52978397 A JP52978397 A JP 52978397A JP 2000504775 A JP2000504775 A JP 2000504775A
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- metal
- carbon atoms
- aryl
- catalyst composition
- 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.)
- Pending
Links
- 239000003054 catalyst Substances 0.000 title claims abstract description 37
- 239000000203 mixture Substances 0.000 title claims abstract description 25
- 150000001875 compounds Chemical class 0.000 claims abstract description 33
- 239000001257 hydrogen Substances 0.000 claims abstract description 27
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 27
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 25
- 125000003118 aryl group Chemical group 0.000 claims abstract description 22
- 238000006243 chemical reaction Methods 0.000 claims abstract description 22
- -1 respectively Ruariru Chemical group 0.000 claims abstract description 22
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 19
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 18
- 150000002736 metal compounds Chemical class 0.000 claims abstract description 14
- 229910052751 metal Inorganic materials 0.000 claims abstract description 12
- 239000002184 metal Substances 0.000 claims abstract description 12
- 125000002877 alkyl aryl group Chemical group 0.000 claims abstract description 11
- 230000000737 periodic effect Effects 0.000 claims abstract description 10
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 9
- 150000002367 halogens Chemical class 0.000 claims abstract description 9
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 7
- 150000001340 alkali metals Chemical class 0.000 claims abstract description 7
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims abstract description 7
- 150000001342 alkaline earth metals Chemical class 0.000 claims abstract description 7
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 7
- 150000002500 ions Chemical class 0.000 claims description 9
- 239000002841 Lewis acid Substances 0.000 claims description 6
- 229910052782 aluminium Inorganic materials 0.000 claims description 5
- 239000000463 material Substances 0.000 claims description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 4
- 229920000098 polyolefin Polymers 0.000 claims description 4
- 150000007517 lewis acids Chemical class 0.000 claims description 3
- 230000007935 neutral effect Effects 0.000 claims description 3
- 229910052740 iodine Inorganic materials 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 4
- 150000002431 hydrogen Chemical class 0.000 abstract description 17
- 238000004519 manufacturing process Methods 0.000 abstract description 13
- 229920000642 polymer Polymers 0.000 abstract description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract description 6
- 150000001336 alkenes Chemical class 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- 238000012685 gas phase polymerization Methods 0.000 abstract 1
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 12
- 239000000047 product Substances 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 6
- 239000005977 Ethylene Substances 0.000 description 6
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical group [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical group [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 6
- 150000001768 cations Chemical class 0.000 description 6
- 239000000460 chlorine Chemical group 0.000 description 6
- 229910052801 chlorine Inorganic materials 0.000 description 6
- 238000006116 polymerization reaction Methods 0.000 description 6
- 229910052719 titanium Inorganic materials 0.000 description 6
- 239000010936 titanium Substances 0.000 description 6
- 229910052726 zirconium Inorganic materials 0.000 description 6
- 239000004698 Polyethylene Substances 0.000 description 5
- 229910052735 hafnium Inorganic materials 0.000 description 5
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical group [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 description 5
- 229920000573 polyethylene Polymers 0.000 description 5
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 4
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000000969 carrier Substances 0.000 description 4
- 125000001309 chloro group Chemical group Cl* 0.000 description 4
- 125000004122 cyclic group Chemical group 0.000 description 4
- 238000009826 distribution Methods 0.000 description 4
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 4
- MCULRUJILOGHCJ-UHFFFAOYSA-N triisobutylaluminium Chemical compound CC(C)C[Al](CC(C)C)CC(C)C MCULRUJILOGHCJ-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 3
- 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 description 3
- 238000001994 activation Methods 0.000 description 3
- 125000000753 cycloalkyl group Chemical group 0.000 description 3
- JLTDJTHDQAWBAV-UHFFFAOYSA-O dimethyl(phenyl)azanium Chemical compound C[NH+](C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-O 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- ORYGRKHDLWYTKX-UHFFFAOYSA-N trihexylalumane Chemical compound CCCCCC[Al](CCCCCC)CCCCCC ORYGRKHDLWYTKX-UHFFFAOYSA-N 0.000 description 3
- VPGLGRNSAYHXPY-UHFFFAOYSA-L zirconium(2+);dichloride Chemical compound Cl[Zr]Cl VPGLGRNSAYHXPY-UHFFFAOYSA-L 0.000 description 3
- LWNGJAHMBMVCJR-UHFFFAOYSA-N (2,3,4,5,6-pentafluorophenoxy)boronic acid Chemical compound OB(O)OC1=C(F)C(F)=C(F)C(F)=C1F LWNGJAHMBMVCJR-UHFFFAOYSA-N 0.000 description 2
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- 239000007848 Bronsted acid Substances 0.000 description 2
- VCFVRHAQERGNFA-UHFFFAOYSA-L C1=CC2=CC=CC=C2C1[Zr](Cl)(Cl)(=[Si](C)C)C1C2=CC=CC=C2C=C1 Chemical compound C1=CC2=CC=CC=C2C1[Zr](Cl)(Cl)(=[Si](C)C)C1C2=CC=CC=C2C=C1 VCFVRHAQERGNFA-UHFFFAOYSA-L 0.000 description 2
- NTWHKVMZCKIKOK-UHFFFAOYSA-N CCCCCCC[Mg]CCCC Chemical compound CCCCCCC[Mg]CCCC NTWHKVMZCKIKOK-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 230000004913 activation Effects 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- QRUYYSPCOGSZGQ-UHFFFAOYSA-L cyclopentane;dichlorozirconium Chemical compound Cl[Zr]Cl.[CH]1[CH][CH][CH][CH]1.[CH]1[CH][CH][CH][CH]1 QRUYYSPCOGSZGQ-UHFFFAOYSA-L 0.000 description 2
- JJQHEAPVGPSOKX-UHFFFAOYSA-L cyclopentyl(trimethyl)silane;dichlorozirconium Chemical compound Cl[Zr]Cl.C[Si](C)(C)[C]1[CH][CH][CH][CH]1.C[Si](C)(C)[C]1[CH][CH][CH][CH]1 JJQHEAPVGPSOKX-UHFFFAOYSA-L 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 125000003106 haloaryl group Chemical group 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical group II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 229910052758 niobium Inorganic materials 0.000 description 2
- 239000010955 niobium Chemical group 0.000 description 2
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical group [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 125000000538 pentafluorophenyl group Chemical group FC1=C(F)C(F)=C(*)C(F)=C1F 0.000 description 2
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 229910052715 tantalum Chemical group 0.000 description 2
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical group [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 2
- 229910052720 vanadium Inorganic materials 0.000 description 2
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical group [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 2
- RSPAIISXQHXRKX-UHFFFAOYSA-L 5-butylcyclopenta-1,3-diene;zirconium(4+);dichloride Chemical compound Cl[Zr+2]Cl.CCCCC1=CC=C[CH-]1.CCCCC1=CC=C[CH-]1 RSPAIISXQHXRKX-UHFFFAOYSA-L 0.000 description 1
- XEZLFNHQVAZJQY-UHFFFAOYSA-L C1CC2CC=CC=C2C1[Zr](Cl)(Cl)(=[Si](C)C)C1C2=CC=CCC2CC1 Chemical compound C1CC2CC=CC=C2C1[Zr](Cl)(Cl)(=[Si](C)C)C1C2=CC=CCC2CC1 XEZLFNHQVAZJQY-UHFFFAOYSA-L 0.000 description 1
- WLHDJFLYFWVYCP-UHFFFAOYSA-L C=C.Cl[Zr](Cl)(C1C=CC=C1)C1C=CC=C1 Chemical compound C=C.Cl[Zr](Cl)(C1C=CC=C1)C1C=CC=C1 WLHDJFLYFWVYCP-UHFFFAOYSA-L 0.000 description 1
- YVKKZIBCKXNVGZ-UHFFFAOYSA-N C[Si](=[Zr](C1C(=CC2=CC=CC=C12)CC1=C(C=CC=C1)C)C1C(=CC2=CC=CC=C12)CC1=C(C=CC=C1)C)C Chemical compound C[Si](=[Zr](C1C(=CC2=CC=CC=C12)CC1=C(C=CC=C1)C)C1C(=CC2=CC=CC=C12)CC1=C(C=CC=C1)C)C YVKKZIBCKXNVGZ-UHFFFAOYSA-N 0.000 description 1
- LMNJIRLUFGKYMP-UHFFFAOYSA-L C[Si](C)=[Zr](Cl)(Cl)(C1C=CC=C1)C1C=CC=C1 Chemical compound C[Si](C)=[Zr](Cl)(Cl)(C1C=CC=C1)C1C=CC=C1 LMNJIRLUFGKYMP-UHFFFAOYSA-L 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- FKLJPTJMIBLJAV-UHFFFAOYSA-N Compound IV Chemical compound O1N=C(C)C=C1CCCCCCCOC1=CC=C(C=2OCCN=2)C=C1 FKLJPTJMIBLJAV-UHFFFAOYSA-N 0.000 description 1
- 241000723368 Conium Species 0.000 description 1
- VVNCNSJFMMFHPL-VKHMYHEASA-N D-penicillamine Chemical group CC(C)(S)[C@@H](N)C(O)=O VVNCNSJFMMFHPL-VKHMYHEASA-N 0.000 description 1
- 102000015782 Electron Transport Complex III Human genes 0.000 description 1
- 108010024882 Electron Transport Complex III Proteins 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 208000037062 Polyps Diseases 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- FOIXSVOLVBLSDH-UHFFFAOYSA-N Silver ion Chemical compound [Ag+] FOIXSVOLVBLSDH-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 229910052770 Uranium Inorganic materials 0.000 description 1
- MMTGZBQNEAVOGW-UHFFFAOYSA-L [Cl-].[Cl-].C(C)[Si](=[Zr+2](C1C(=CC2=CC=CC=C12)C)C1C(=CC2=CC=CC=C12)C)CC Chemical compound [Cl-].[Cl-].C(C)[Si](=[Zr+2](C1C(=CC2=CC=CC=C12)C)C1C(=CC2=CC=CC=C12)C)CC MMTGZBQNEAVOGW-UHFFFAOYSA-L 0.000 description 1
- DLQZGRLCYQJIDQ-UHFFFAOYSA-L [Cl-].[Cl-].C=C.C12=CC=CCC2CCC1[Zr+2]C1C2=CC=CCC2CC1 Chemical compound [Cl-].[Cl-].C=C.C12=CC=CCC2CCC1[Zr+2]C1C2=CC=CCC2CC1 DLQZGRLCYQJIDQ-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
- GCPXODGHANPVBD-UHFFFAOYSA-L [Cl-].[Cl-].CC(C)C1=Cc2ccccc2C1[Zr++](C1C(=Cc2ccccc12)C(C)C)=[Si](C)C Chemical compound [Cl-].[Cl-].CC(C)C1=Cc2ccccc2C1[Zr++](C1C(=Cc2ccccc12)C(C)C)=[Si](C)C GCPXODGHANPVBD-UHFFFAOYSA-L 0.000 description 1
- AFJNDIIQUIATSM-UHFFFAOYSA-L [Cl-].[Cl-].C[Si](=[Zr+2](C1C=C(C=C1CC)C(C)(C)C)C1C=C(C=C1CC)C(C)(C)C)C Chemical compound [Cl-].[Cl-].C[Si](=[Zr+2](C1C=C(C=C1CC)C(C)(C)C)C1C=C(C=C1CC)C(C)(C)C)C AFJNDIIQUIATSM-UHFFFAOYSA-L 0.000 description 1
- GPTVXHHNFZPTOX-UHFFFAOYSA-L [Cl-].[Cl-].C[Si](C)=[Zr++]([C@H]1C(=Cc2ccccc12)C(C)(C)C)[C@@H]1C(=Cc2ccccc12)C(C)(C)C Chemical compound [Cl-].[Cl-].C[Si](C)=[Zr++]([C@H]1C(=Cc2ccccc12)C(C)(C)C)[C@@H]1C(=Cc2ccccc12)C(C)(C)C GPTVXHHNFZPTOX-UHFFFAOYSA-L 0.000 description 1
- 125000005234 alkyl aluminium group Chemical group 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- UORVGPXVDQYIDP-BJUDXGSMSA-N borane Chemical class [10BH3] UORVGPXVDQYIDP-BJUDXGSMSA-N 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 238000012662 bulk polymerization Methods 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
- 238000003763 carbonization Methods 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 125000004965 chloroalkyl group Chemical group 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 150000001925 cycloalkenes Chemical class 0.000 description 1
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 description 1
- 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 description 1
- PDPHVMXUMPVVBZ-UHFFFAOYSA-L dichlorozirconium;ethylcyclopentane Chemical compound Cl[Zr]Cl.CC[C]1[CH][CH][CH][CH]1.CC[C]1[CH][CH][CH][CH]1 PDPHVMXUMPVVBZ-UHFFFAOYSA-L 0.000 description 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 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical group O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910052732 germanium Inorganic materials 0.000 description 1
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000001282 iso-butane Substances 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000012968 metallocene catalyst Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000000877 morphologic effect Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229940054334 silver cation Drugs 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- ZWYDDDAMNQQZHD-UHFFFAOYSA-L titanium(ii) chloride Chemical compound [Cl-].[Cl-].[Ti+2] ZWYDDDAMNQQZHD-UHFFFAOYSA-L 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 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 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- 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
- C08F4/619—Component covered by group C08F4/60 containing a transition metal-carbon bond
- C08F4/61916—Component covered by group C08F4/60 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
- 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
- C08F110/00—Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F110/02—Ethene
-
- 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
- C08F110/00—Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F110/04—Monomers containing three or four carbon atoms
- C08F110/06—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
- C08F4/00—Polymerisation catalysts
- C08F4/02—Carriers therefor
- C08F4/025—Metal oxides
-
- 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
- C08F4/619—Component covered by group C08F4/60 containing a transition metal-carbon bond
- C08F4/61908—Component covered by group C08F4/60 containing a transition metal-carbon bond in combination with an ionising compound other than alumoxane, e.g. (C6F5)4B-X+
-
- 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
- C08F4/619—Component covered by group C08F4/60 containing a transition metal-carbon bond
- C08F4/61912—Component covered by group C08F4/60 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
- C08F4/619—Component covered by group C08F4/60 containing a transition metal-carbon bond
- C08F4/6192—Component covered by group C08F4/60 containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring
- C08F4/61922—Component covered by group C08F4/60 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
- 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)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Crystallography & Structural Chemistry (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Claims (1)
- 【特許請求の範囲】 1.(A)無機担体と、以下の一般式I M1(R1)r(R2)s(R3)t(R4)u I で表わされ、かつ式中の M1がアルカリ金属、アルカリ土類金属または周期表のIIIまたはIV主族 金属、 R1が水素、C1−C10アルキル、C6−C15アリール、アルキル基中に1から 10個、アリール基中に6から20個の炭素原子を有するアルキルアリールまた はアリールアルキル、 R2からR4が、それぞれ水素、ハロゲン、C1−C10アルキル、C6−C15アリ ール、アルキル基中に1から10個、アリール基中に6から20個の炭素原子を それぞれ有するアルキルアリール、アリールアルキル、アルコキシまたはジアル キルアミノ、 rが1から4の整数、 s、tおよびuが0から3の整数を意味するが、r+s+t+uの合計がM1 の原子価に対応する金属化合物との反応、 (B)上記反応(A)により得られる化合物と、金属ジハロゲン化物の形態に おけるメタロセン錯体およびメタロセニウムイオン形成化合物との反応、および (C)これに次いで、以下の一般式II M2(R5)o(R6)p(R7)q II で表わされ、かつ式中の M2がアルカリ金属、アルカリ土類金属または周期表のIII主族金属、 R5が水素、C1−C10アルキル、C6−C15アリール、アルキル基中に1から 10個、アリール基中に6から20個の炭素原子を有するアルキルアリールまた はアリールアルキル、 R6、R7がそれぞれ水素、ハロゲン、C1−C10アルキル、C6−C15アリール 、アルキル基中に1から10個、アリール基中に6から20個の炭素原子をそれ ぞれ有するアルキルアリール、アリールアルキル、アルコキシ、 oが1から3の整数、 p、qがそれぞれ0から2の整数を意味するが、o+p+qの合計がM2の原 子価に対応する場合の金属化合物との反応により得られることを特徴とする、担 持触媒組成物。 2.工程(A)において得られる材料が単離され、乾燥されることを特徴とす る、請求項1の担持触媒組成物。 3.式I中のM1がアルミニウム、R1からR3がそれぞれC1−C10アルキル、 uが零を意味することを特徴とする、請求項1または2の担持触媒組成物。 4.メタロセニウム形成化合物として、強、中性ルイス酸、ルイス酸カチオン を有するイオン結合化合物、およびカチオンとしてブレンステッド酸を有するイ オン結合化合物の中から選ばれる配位錯化合物が使用されることを特徴とする、 請求項1から3のいずれかの担持触媒組成物。 5.式II中のR5からR7が、それぞれC1−C10アルキルを意味することを 特徴とする、請求項1から4のいずれかの担持触媒組成物。 6.請求項1の条件下に担持触媒組成物を製造することを特徴とする、請求項 1から5のいずれかの担持触媒組成物。 7.請求項1から5のいずれかの担持触媒組成物の、ポリオレフィン製造のた めの用途。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19606167A DE19606167A1 (de) | 1996-02-20 | 1996-02-20 | Geträgerte Katalysatorsysteme |
DE19606167.9 | 1996-02-20 | ||
PCT/EP1997/000769 WO1997031038A1 (de) | 1996-02-20 | 1997-02-19 | Geträgerte katalysatorsysteme |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2000504775A true JP2000504775A (ja) | 2000-04-18 |
JP2000504775A5 JP2000504775A5 (ja) | 2004-11-25 |
Family
ID=7785836
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9529783A Pending JP2000504775A (ja) | 1996-02-20 | 1997-02-19 | 担持触媒組成物 |
Country Status (14)
Country | Link |
---|---|
US (1) | US6350829B1 (ja) |
EP (1) | EP0882076B1 (ja) |
JP (1) | JP2000504775A (ja) |
KR (1) | KR100472687B1 (ja) |
CN (1) | CN1246345C (ja) |
AT (1) | ATE200786T1 (ja) |
AU (1) | AU711554B2 (ja) |
BR (1) | BR9707570A (ja) |
CA (1) | CA2246360A1 (ja) |
DE (2) | DE19606167A1 (ja) |
ES (1) | ES2156358T3 (ja) |
NO (1) | NO983785L (ja) |
TW (1) | TW469276B (ja) |
WO (1) | WO1997031038A1 (ja) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002518560A (ja) * | 1998-06-25 | 2002-06-25 | バーゼル、ポリオレフィン、ゲゼルシャフト、ミット、ベシュレンクテル、ハフツング | 担持触媒の製造 |
JP2009144026A (ja) * | 2007-12-13 | 2009-07-02 | Japan Polypropylene Corp | プロピレン(共)重合体の製造方法 |
Families Citing this family (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19757262A1 (de) * | 1997-12-23 | 1999-07-01 | Targor Gmbh | Verfahren zur Herstellung von Olefinpolymerisaten mit erhöhtem Schmelzpunkt |
WO1998040419A1 (de) * | 1997-03-07 | 1998-09-17 | Targor Gmbh | Verfahren zur herstellung von olefinpolymerisaten mit erhöhtem schmelzpunkt |
DE19806435A1 (de) | 1998-02-17 | 1999-08-19 | Basf Ag | Verfahren zur Herstellung eines geträgerten Katalysatorsystems |
DE19811934A1 (de) | 1998-03-19 | 1999-09-23 | Basf Ag | Ethylencopolymere mit enger Comonomerverteilung |
DE19957384A1 (de) | 1999-11-29 | 2001-05-31 | Targor Gmbh | Hochmolekulares Polypropylen mit breiter Molekulargewichtsverteilung und geringer isotaktischer Sequenzlänge |
JP4901043B2 (ja) | 1999-12-23 | 2012-03-21 | バーゼル、ポリプロピレン、ゲゼルシャフト、ミット、ベシュレンクテル、ハフツング | 遷移金属化合物、配位子組成物、触媒組成物及びこれをオレフィンの重合及び共重合に使用する方法 |
DE50112718D1 (de) | 2000-05-31 | 2007-08-23 | Basell Polyolefine Gmbh | Verfahren zur herstellung von übergangsmetallverbindungen und deren verwendung zur polymerisation von olefinen |
DE10057009A1 (de) | 2000-11-17 | 2002-05-29 | Celanese Ventures Gmbh | Non-Metallocene, Verfahren zur Herstellung von diesen und deren Verwendung zur Polymerisation von Olefinen |
CN1525976A (zh) * | 2001-02-17 | 2004-09-01 | �����ɷ� | 非金属茂、其生产方法及其在烯烃聚合中的用途 |
CN1491235A (zh) * | 2001-02-17 | 2004-04-21 | 赛拉尼斯温特斯股份有限公司 | 作为催化剂组分的过渡金属化合物及其在生产聚烯烃中的用途 |
DE10130229A1 (de) | 2001-06-22 | 2003-01-02 | Celanese Ventures Gmbh | Non-Metallocene, Verfahren zur Herstellung von diesen und deren Verwendung zur Polymerisation von Olefinen |
DE10208252A1 (de) | 2002-02-26 | 2003-09-04 | Celanese Ventures Gmbh | Konvalent fixierte Non-Metallocene, Verfahren zur Herstellung von diesen und deren Verwendung zur Polymerisation von Olefinen |
JP4972284B2 (ja) * | 2002-10-15 | 2012-07-11 | エクソンモービル・ケミカル・パテンツ・インク | オレフィン重合のための複数触媒系及びそれらから生成されたポリマー |
US7700707B2 (en) | 2002-10-15 | 2010-04-20 | Exxonmobil Chemical Patents Inc. | Polyolefin adhesive compositions and articles made therefrom |
US7550528B2 (en) * | 2002-10-15 | 2009-06-23 | Exxonmobil Chemical Patents Inc. | Functionalized olefin polymers |
US7223822B2 (en) * | 2002-10-15 | 2007-05-29 | Exxonmobil Chemical Patents Inc. | Multiple catalyst and reactor system for olefin polymerization and polymers produced therefrom |
US7541402B2 (en) * | 2002-10-15 | 2009-06-02 | Exxonmobil Chemical Patents Inc. | Blend functionalized polyolefin adhesive |
US7285608B2 (en) | 2004-04-21 | 2007-10-23 | Novolen Technology Holdings C.V. | Metallocene ligands, metallocene compounds and metallocene catalysts, their synthesis and their use for the polymerization of olefins |
US7598329B2 (en) * | 2005-11-04 | 2009-10-06 | Ticona Gmbh | Process for manufacturing ultra high molecular weight polymers using novel bridged metallocene catalysts |
US8034886B2 (en) | 2005-11-04 | 2011-10-11 | Ticona Gmbh | Process for manufacturing high to ultra high molecular weight polymers using novel bridged metallocene catalysts |
EP1847555A1 (en) | 2006-04-18 | 2007-10-24 | Borealis Technology Oy | Multi-branched Polypropylene |
KR101278336B1 (ko) | 2007-10-25 | 2013-06-25 | 루머스 노보렌 테크놀로지 게엠베하 | 안사-메탈로센 화합물의 라세모선택적 합성, 안사-메탈로센 화합물, 이를 포함하는 촉매, 그 촉매를 이용한 올레핀 폴리머 제조 공정, 그리고 올레핀 호모- 및 코폴리머 |
WO2009054833A2 (en) | 2007-10-25 | 2009-04-30 | Novolen Technology Holdings, C.V. | Metallocene compounds, catalysts comprising them, process for producing an olefin polymer by use of the catalysts, and olefin homo and copolymers |
WO2009054832A1 (en) * | 2007-10-25 | 2009-04-30 | Novolen Technology Holdings, C.V. | Metallocene compounds, catalysts comprising them, process for producing an olefin polymer by use of the catalysts, and olefin homo-and copolymers |
US20120142882A1 (en) | 2009-01-23 | 2012-06-07 | Evonik Oxeno Gmbh | Pe mib slurry polymerisation |
JP5787769B2 (ja) | 2009-01-23 | 2015-09-30 | エボニック デグサ ゲーエムベーハーEvonik Degussa GmbH | 3置換c4−10アルケンとのポリオレフィン気相重合 |
WO2010084049A1 (en) | 2009-01-23 | 2010-07-29 | Evonik Oxeno Gmbh | Film |
GB2498936A (en) | 2012-01-31 | 2013-08-07 | Norner Innovation As | Polyethylene with multi-modal molecular weight distribution |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4912075A (en) | 1987-12-17 | 1990-03-27 | Exxon Chemical Patents Inc. | Method for preparing a supported metallocene-alumoxane catalyst for gas phase polymerization |
WO1991009882A1 (en) | 1990-01-02 | 1991-07-11 | Exxon Chemical Patents Inc. | Supported ionic metallocene catalysts for olefin polymerization |
EP0841349B1 (en) * | 1990-07-24 | 2002-06-12 | Mitsui Chemicals, Inc. | Catalyst for alpha-olefin polymerization and production of poly-alpha-olefin therewith |
EP0522581B1 (en) * | 1991-07-11 | 1997-10-15 | Idemitsu Kosan Company Limited | Process for producing olefin based polymers and olefin polymerization catalyst |
ES2167336T3 (es) | 1992-08-05 | 2002-05-16 | Exxonmobil Chem Patents Inc | Catalizadores ionicos soportados de metal de transicion para la polimerizacion de olefinas. |
JP3202349B2 (ja) * | 1992-09-22 | 2001-08-27 | 三菱化学株式会社 | 触媒組成物およびそれを用いるオレフィンの重合法 |
BE1006880A3 (fr) | 1993-03-01 | 1995-01-17 | Solvay | Precurseur solide d'un systeme catalytique pour la polymerisation d'olefines, procede pour sa preparation, systeme catalytique comprenant ce precurseur solide et procede de polymerisation d'olefines en presence de ce systeme catalytique. |
DE69403928T2 (de) * | 1993-04-09 | 1997-12-18 | Tosoh Corp | Katalysator und Verfahren zur Olefin-Polymerisation |
DE69431222T2 (de) * | 1993-06-07 | 2003-04-17 | Mitsui Chemicals Inc | Übergangsmetallverbindung, und diese enthaltender Polymerisationkatalysator |
JP2882241B2 (ja) * | 1993-06-07 | 1999-04-12 | 東ソー株式会社 | オレフィン重合用触媒およびオレフィンの重合方法 |
US5422325A (en) * | 1993-09-17 | 1995-06-06 | Exxon Chemical Patents Inc. | Supported polymerization catalysts, their production and use |
CA2176950C (en) * | 1993-11-19 | 2006-01-31 | Moses Olukayode Jejelowo | Polymerization catalyst systems, their production and use |
US5498582A (en) * | 1993-12-06 | 1996-03-12 | Mobil Oil Corporation | Supported metallocene catalysts for the production of polyolefins |
DE4431837A1 (de) * | 1994-09-07 | 1996-03-14 | Basf Ag | Geträgerte Metallocen-Katalysatorsysteme |
DE4431838A1 (de) * | 1994-09-07 | 1996-03-14 | Basf Ag | Geträgerte Metallocen-Katalysatorsysteme |
-
1996
- 1996-02-20 DE DE19606167A patent/DE19606167A1/de not_active Withdrawn
-
1997
- 1997-02-19 AU AU17919/97A patent/AU711554B2/en not_active Ceased
- 1997-02-19 CA CA002246360A patent/CA2246360A1/en not_active Abandoned
- 1997-02-19 AT AT97903319T patent/ATE200786T1/de not_active IP Right Cessation
- 1997-02-19 WO PCT/EP1997/000769 patent/WO1997031038A1/de active IP Right Grant
- 1997-02-19 ES ES97903319T patent/ES2156358T3/es not_active Expired - Lifetime
- 1997-02-19 CN CNB971924007A patent/CN1246345C/zh not_active Expired - Fee Related
- 1997-02-19 DE DE59703436T patent/DE59703436D1/de not_active Expired - Lifetime
- 1997-02-19 JP JP9529783A patent/JP2000504775A/ja active Pending
- 1997-02-19 KR KR10-1998-0706452A patent/KR100472687B1/ko not_active IP Right Cessation
- 1997-02-19 US US09/125,377 patent/US6350829B1/en not_active Expired - Fee Related
- 1997-02-19 EP EP97903319A patent/EP0882076B1/de not_active Expired - Lifetime
- 1997-02-19 BR BR9707570A patent/BR9707570A/pt not_active IP Right Cessation
- 1997-02-19 TW TW086101973A patent/TW469276B/zh active
-
1998
- 1998-08-19 NO NO983785A patent/NO983785L/no not_active Application Discontinuation
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002518560A (ja) * | 1998-06-25 | 2002-06-25 | バーゼル、ポリオレフィン、ゲゼルシャフト、ミット、ベシュレンクテル、ハフツング | 担持触媒の製造 |
JP2009144026A (ja) * | 2007-12-13 | 2009-07-02 | Japan Polypropylene Corp | プロピレン(共)重合体の製造方法 |
Also Published As
Publication number | Publication date |
---|---|
CN1246345C (zh) | 2006-03-22 |
KR19990087066A (ko) | 1999-12-15 |
ES2156358T3 (es) | 2001-06-16 |
EP0882076B1 (de) | 2001-04-25 |
BR9707570A (pt) | 1999-07-27 |
DE19606167A1 (de) | 1997-08-21 |
TW469276B (en) | 2001-12-21 |
US6350829B1 (en) | 2002-02-26 |
CA2246360A1 (en) | 1997-08-28 |
AU711554B2 (en) | 1999-10-14 |
NO983785L (no) | 1998-10-19 |
CN1211996A (zh) | 1999-03-24 |
KR100472687B1 (ko) | 2005-05-16 |
EP0882076A1 (de) | 1998-12-09 |
DE59703436D1 (de) | 2001-05-31 |
NO983785D0 (no) | 1998-08-19 |
ATE200786T1 (de) | 2001-05-15 |
AU1791997A (en) | 1997-09-10 |
WO1997031038A1 (de) | 1997-08-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP2000504775A (ja) | 担持触媒組成物 | |
KR100470842B1 (ko) | 담지된메탈로센촉매계및대전방지제의존재하에1-알켄의중합체를제조하는방법 | |
US5753773A (en) | Multiphase block of propylene, comprising copolymers of propylene | |
US5691264A (en) | Components and catalysts for the polymerization of olefins | |
AU630451B2 (en) | Process for the preparation of ethylene polymers | |
JP2002523568A (ja) | 高度に活性な担持触媒組成物 | |
CA2168210A1 (en) | Components and catalysts for the polymerization of olefins | |
JP2001501987A (ja) | 遷移金属担持触媒の製造方法 | |
JP3785423B2 (ja) | 懸濁重合によるエチレン重合体の製造方法 | |
US6433111B1 (en) | Method for producing a supported catalyst system | |
US6433110B1 (en) | Process for producing alkene polymers by gas phase polymerisation | |
JP2000504776A (ja) | 懸濁重合によるアルケン重合体の製造方法 | |
JPH08176219A (ja) | メタロセン担体触媒組成物 | |
US6683018B1 (en) | Method for producing a supported catalyst system | |
JP3907270B2 (ja) | 反応遅延剤を添加するc2−c12アルケンポリマーの製造方法 | |
JP3117257B2 (ja) | ポリオレフィン製造用固体触媒およびポリオレフィンの製造方法 | |
JP2000511959A (ja) | 担体として無機酸化物を有するメタロセン触媒組成物 | |
JP3102929B2 (ja) | ポリオレフィン製造用固体触媒およびポリオレフィンの製造方法 | |
BRPI0418117B1 (pt) | preparação de cocatalisadores suportados | |
JP2002513049A (ja) | 活性化剤フッ化アルミニウムを伴った触媒組成物 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20040213 |
|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20040213 |
|
A711 | Notification of change in applicant |
Free format text: JAPANESE INTERMEDIATE CODE: A711 Effective date: 20060123 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20060228 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20050915 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20060526 |
|
A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20060710 |
|
A524 | Written submission of copy of amendment under article 19 pct |
Free format text: JAPANESE INTERMEDIATE CODE: A524 Effective date: 20060718 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20060905 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20061115 |
|
A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20070105 |
|
A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20070605 |