CN1267460C - 催化组合物、其制备方法、聚合体系和制备加聚物的方法 - Google Patents
催化组合物、其制备方法、聚合体系和制备加聚物的方法 Download PDFInfo
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- CN1267460C CN1267460C CNB2004100641613A CN200410064161A CN1267460C CN 1267460 C CN1267460 C CN 1267460C CN B2004100641613 A CNB2004100641613 A CN B2004100641613A CN 200410064161 A CN200410064161 A CN 200410064161A CN 1267460 C CN1267460 C CN 1267460C
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- alkyl
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- 239000000178 monomer Substances 0.000 title claims abstract description 168
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- 238000002360 preparation method Methods 0.000 title claims abstract description 54
- 125000002091 cationic group Chemical group 0.000 claims abstract description 147
- 238000000034 method Methods 0.000 claims abstract description 96
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 61
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- 239000002184 metal Substances 0.000 claims description 490
- 239000002243 precursor Substances 0.000 claims description 124
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 102
- 125000000217 alkyl group Chemical group 0.000 claims description 102
- 239000000126 substance Substances 0.000 claims description 71
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 61
- 229910052763 palladium Inorganic materials 0.000 claims description 51
- 150000001336 alkenes Chemical class 0.000 claims description 46
- 239000011572 manganese Substances 0.000 claims description 38
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 34
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 33
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- 239000004332 silver Substances 0.000 claims description 33
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 32
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- 125000000129 anionic group Chemical group 0.000 claims description 30
- 229910052759 nickel Inorganic materials 0.000 claims description 28
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 24
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- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 16
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- 239000010941 cobalt Substances 0.000 claims description 16
- 229910052802 copper Inorganic materials 0.000 claims description 16
- 239000010949 copper Substances 0.000 claims description 16
- 229910052742 iron Inorganic materials 0.000 claims description 16
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 12
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 12
- 229910052804 chromium Inorganic materials 0.000 claims description 12
- 239000011651 chromium Substances 0.000 claims description 12
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims description 12
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- 239000010948 rhodium Substances 0.000 claims description 12
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- 229910052796 boron Inorganic materials 0.000 claims description 5
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- 125000004429 atom Chemical group 0.000 description 251
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- 239000000243 solution Substances 0.000 description 239
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- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 46
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 43
- 125000003118 aryl group Chemical group 0.000 description 43
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- 239000003446 ligand Substances 0.000 description 39
- 239000003054 catalyst Substances 0.000 description 37
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 36
- 239000000047 product Substances 0.000 description 36
- 125000000538 pentafluorophenyl group Chemical group FC1=C(F)C(F)=C(*)C(F)=C1F 0.000 description 35
- 229910052782 aluminium Chemical group 0.000 description 34
- 229910052799 carbon Inorganic materials 0.000 description 33
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- 229910052739 hydrogen Inorganic materials 0.000 description 31
- 239000001257 hydrogen Substances 0.000 description 31
- 239000000463 material Substances 0.000 description 31
- 229910052757 nitrogen Inorganic materials 0.000 description 31
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- 150000002367 halogens Chemical class 0.000 description 30
- 210000002966 serum Anatomy 0.000 description 29
- 238000003756 stirring Methods 0.000 description 29
- WLPUWLXVBWGYMZ-UHFFFAOYSA-N tricyclohexylphosphine Chemical compound C1CCCCC1P(C1CCCCC1)C1CCCCC1 WLPUWLXVBWGYMZ-UHFFFAOYSA-N 0.000 description 29
- 238000006243 chemical reaction Methods 0.000 description 27
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- 239000004411 aluminium Chemical group 0.000 description 26
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 25
- 239000002253 acid Substances 0.000 description 25
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical group [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 24
- 239000002585 base Substances 0.000 description 24
- XYFCBTPGUUZFHI-UHFFFAOYSA-N phosphine group Chemical group P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 24
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 24
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 23
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 22
- 238000001914 filtration Methods 0.000 description 22
- 229920001519 homopolymer Polymers 0.000 description 22
- 150000002431 hydrogen Chemical group 0.000 description 22
- 238000005160 1H NMR spectroscopy Methods 0.000 description 21
- 150000002500 ions Chemical class 0.000 description 21
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 20
- 125000003545 alkoxy group Chemical group 0.000 description 20
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 20
- 230000008878 coupling Effects 0.000 description 19
- 238000010168 coupling process Methods 0.000 description 19
- 238000005859 coupling reaction Methods 0.000 description 19
- PSHMSSXLYVAENJ-UHFFFAOYSA-N dilithium;[oxido(oxoboranyloxy)boranyl]oxy-oxoboranyloxyborinate Chemical compound [Li+].[Li+].O=BOB([O-])OB([O-])OB=O PSHMSSXLYVAENJ-UHFFFAOYSA-N 0.000 description 19
- 238000005227 gel permeation chromatography Methods 0.000 description 19
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 18
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- 125000000524 functional group Chemical group 0.000 description 18
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- 125000000753 cycloalkyl group Chemical group 0.000 description 17
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 16
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- JFNLZVQOOSMTJK-ULUSZKPHSA-N (4r)-bicyclo[2.2.1]hept-2-ene Chemical group C1C2CC[C@H]1C=C2 JFNLZVQOOSMTJK-ULUSZKPHSA-N 0.000 description 15
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- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 14
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- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 14
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- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 10
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- 125000005005 perfluorohexyl group Chemical group FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)* 0.000 description 1
- 125000005062 perfluorophenyl group Chemical group FC1=C(C(=C(C(=C1F)F)F)F)* 0.000 description 1
- 125000005009 perfluoropropyl group Chemical group FC(C(C(F)(F)F)(F)F)(F)* 0.000 description 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical group [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 description 1
- 125000005538 phosphinite group Chemical group 0.000 description 1
- 150000008301 phosphite esters Chemical class 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
- 150000004714 phosphonium salts Chemical class 0.000 description 1
- 125000004437 phosphorous atom Chemical group 0.000 description 1
- 239000011295 pitch Substances 0.000 description 1
- 229920006112 polar polymer Polymers 0.000 description 1
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- 229920000636 poly(norbornene) polymer Polymers 0.000 description 1
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- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
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- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- QTECDUFMBMSHKR-UHFFFAOYSA-N prop-2-enyl prop-2-enoate Chemical compound C=CCOC(=O)C=C QTECDUFMBMSHKR-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
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- 238000010107 reaction injection moulding Methods 0.000 description 1
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- 239000013557 residual solvent Substances 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- 239000012945 sealing adhesive Substances 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 230000009919 sequestration Effects 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 1
- 238000006884 silylation reaction Methods 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
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- 230000006641 stabilisation Effects 0.000 description 1
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- 239000011550 stock solution Substances 0.000 description 1
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- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 description 1
- 229910052716 thallium Inorganic materials 0.000 description 1
- BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical compound [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 125000005309 thioalkoxy group Chemical group 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 150000003613 toluenes Chemical class 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- SQBBHCOIQXKPHL-UHFFFAOYSA-N tributylalumane Chemical compound CCCC[Al](CCCC)CCCC SQBBHCOIQXKPHL-UHFFFAOYSA-N 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- BDZBKCUKTQZUTL-UHFFFAOYSA-N triethyl phosphite Chemical compound CCOP(OCC)OCC BDZBKCUKTQZUTL-UHFFFAOYSA-N 0.000 description 1
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 1
- WWVNWQJKWKSDQM-UHFFFAOYSA-N triethylarsane Chemical compound CC[As](CC)CC WWVNWQJKWKSDQM-UHFFFAOYSA-N 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- QQAHNNMLPUNNNJ-UHFFFAOYSA-N trifluoromethylphosphane Chemical compound FC(F)(F)P QQAHNNMLPUNNNJ-UHFFFAOYSA-N 0.000 description 1
- JLTRXTDYQLMHGR-UHFFFAOYSA-N trimethylaluminium Chemical compound C[Al](C)C JLTRXTDYQLMHGR-UHFFFAOYSA-N 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- LFXVBWRMVZPLFK-UHFFFAOYSA-N trioctylalumane Chemical compound CCCCCCCC[Al](CCCCCCCC)CCCCCCCC LFXVBWRMVZPLFK-UHFFFAOYSA-N 0.000 description 1
- BPLUKJNHPBNVQL-UHFFFAOYSA-N triphenylarsine Chemical compound C1=CC=CC=C1[As](C=1C=CC=CC=1)C1=CC=CC=C1 BPLUKJNHPBNVQL-UHFFFAOYSA-N 0.000 description 1
- MXSVLWZRHLXFKH-UHFFFAOYSA-N triphenylborane Chemical compound C1=CC=CC=C1B(C=1C=CC=CC=1)C1=CC=CC=C1 MXSVLWZRHLXFKH-UHFFFAOYSA-N 0.000 description 1
- CNWZYDSEVLFSMS-UHFFFAOYSA-N tripropylalumane Chemical compound CCC[Al](CCC)CCC CNWZYDSEVLFSMS-UHFFFAOYSA-N 0.000 description 1
- 125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- OLFPYUPGPBITMH-UHFFFAOYSA-N tritylium Chemical compound C1=CC=CC=C1[C+](C=1C=CC=CC=1)C1=CC=CC=C1 OLFPYUPGPBITMH-UHFFFAOYSA-N 0.000 description 1
- 238000002328 two-dimensional heteronuclear correlation spectroscopy Methods 0.000 description 1
- 238000012725 vapour phase polymerization Methods 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N vinyl ethyl ether Natural products CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 1
- 239000012905 visible particle Substances 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
- 229910052726 zirconium Inorganic materials 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
- C08F4/50—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 selected from alkaline earth metals, zinc, cadmium, mercury, copper or silver
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/04—Nickel compounds
-
- 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
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/10—Esters
- C08F20/12—Esters of monohydric alcohols or phenols
-
- 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
-
- 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
- C08F210/02—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
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/14—Monomers containing five or more carbon atoms
-
- 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
- C08F2410/00—Features related to the catalyst preparation, the catalyst use or to the deactivation of the catalyst
- C08F2410/03—Multinuclear procatalyst, i.e. containing two or more metals, being different or not
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymerization Catalysts (AREA)
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US49687303P | 2003-08-21 | 2003-08-21 | |
| US60/496,873 | 2003-08-21 | ||
| US55924304P | 2004-04-02 | 2004-04-02 | |
| US60/559,243 | 2004-04-02 | ||
| US10/857,330 US7087687B2 (en) | 2003-08-21 | 2004-05-28 | Catalytic composition and its preparation and use for preparing polymers from ethylenically unsaturated monomers |
| US10/857,330 | 2004-05-28 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1597709A CN1597709A (zh) | 2005-03-23 |
| CN1267460C true CN1267460C (zh) | 2006-08-02 |
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| US (1) | US7087687B2 (enExample) |
| EP (1) | EP1508577A1 (enExample) |
| JP (1) | JP2005068424A (enExample) |
| KR (1) | KR100560061B1 (enExample) |
| CN (1) | CN1267460C (enExample) |
| TW (1) | TWI262196B (enExample) |
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| US7087687B2 (en) * | 2003-08-21 | 2006-08-08 | Rohm And Haas Company | Catalytic composition and its preparation and use for preparing polymers from ethylenically unsaturated monomers |
| US7208541B2 (en) * | 2003-08-22 | 2007-04-24 | National Starch And Chemical Investment Holding Corporation | Hot melt adhesive |
| US7172986B2 (en) * | 2004-06-14 | 2007-02-06 | Rohm And Haas Company | Catalytic composition and its preparation and use for preparing polymers from ethylenically unsaturated monomers |
| US7199074B2 (en) * | 2004-06-14 | 2007-04-03 | Rohm And Haas Company | Catalytic composition and its preparation and use for preparing polymers from ethylenically unsaturated monomers |
| US7595369B2 (en) * | 2004-11-10 | 2009-09-29 | Lg Chem, Ltd. | Method of polymerizing cyclic olefins and vinyl olefins, copolymer produced by the method and optical anisotropic film comprising the same |
| US7749934B2 (en) * | 2005-02-22 | 2010-07-06 | Rohm And Haas Company | Protected catalytic composition and its preparation and use for preparing polymers from ethylenically unsaturated monomers |
| US7435701B2 (en) * | 2005-05-27 | 2008-10-14 | Rohm And Haas Company | Catalytic composition and its preparation and use for preparing polymers from ethylenically unsaturated monomers |
| US7635739B2 (en) | 2005-08-31 | 2009-12-22 | Rohm And Haas Company | Substantially linear polymers and methods of making and using same |
| JP4855740B2 (ja) * | 2005-09-01 | 2012-01-18 | 株式会社クラレ | 金属化合物、金属化合物を含むビニルエステル系モノマー重合用触媒組成物およびそのビニルエステル系モノマーの重合への使用 |
| JP2007063470A (ja) * | 2005-09-01 | 2007-03-15 | Kuraray Co Ltd | 金属化合物、金属化合物を含むビニル系モノマー重合用触媒組成物およびそのビニル系モノマーの重合への使用 |
| KR100882315B1 (ko) * | 2006-04-28 | 2009-02-10 | 주식회사 엘지화학 | 루이스 산을 이용한 α-올레핀-아크릴레이트-노보넨 3원공중합체 제조방법 및 이에 의해 제조된 공중합체 |
| KR101540820B1 (ko) * | 2006-11-14 | 2015-07-30 | 유니베이션 테크놀로지즈, 엘엘씨 | 촉매계 및 중합 방법 |
| US20080118570A1 (en) * | 2006-11-20 | 2008-05-22 | Zhi Liu | Polymer coated drug-ion exchange resins and methods |
| JP2009096970A (ja) * | 2007-01-31 | 2009-05-07 | Sumitomo Bakelite Co Ltd | 環状オレフィン系ポリマーの製造方法 |
| CA2620884C (en) * | 2007-02-28 | 2011-07-12 | Rohm And Haas Company | Composition and method for preparing copolymers of polar and non-polar olefins substantially free of free radical intiated polymer |
| JP5016512B2 (ja) | 2007-02-28 | 2012-09-05 | ローム アンド ハース カンパニー | 実質的に線状のコポリマーおよびその製造方法 |
| JP5111145B2 (ja) | 2007-02-28 | 2012-12-26 | ローム アンド ハース カンパニー | 非環式脂肪族オレフィンの重合 |
| CA2620852A1 (en) | 2007-02-28 | 2008-08-28 | Rohm And Haas Company | A porous linear polymer composition and method of making same |
| FR2937643B1 (fr) * | 2008-10-27 | 2011-10-14 | Arkema France | Nouveaux copolymeres a blocs d'olefines polaires et apolaires |
| JP5738097B2 (ja) * | 2010-09-10 | 2015-06-17 | 昭和電工株式会社 | ノルボルネン系重合体の製造方法 |
| JP5834017B2 (ja) * | 2010-10-26 | 2015-12-16 | 昭和電工株式会社 | ノルボルネン系モノマー重合用触媒及びノルボルネン系重合体の製造方法 |
| JP2012121956A (ja) * | 2010-12-07 | 2012-06-28 | Sumitomo Bakelite Co Ltd | 付加型ノルボルネン系樹脂、その製造方法、該樹脂を含む樹脂組成物、ならびに該樹脂を含む成形体および該成形体を含む複合部材 |
| WO2012164574A1 (en) | 2011-05-09 | 2012-12-06 | Reliance Industries Limited | Nitrogen containing external donor system for propylene polymerization |
| JP5575702B2 (ja) * | 2011-05-20 | 2014-08-20 | 株式会社クラレ | ビニル系モノマー重合用触媒組成物および該組成物を用いたビニル系モノマーの重合への使用 |
| EP2980107B1 (en) | 2013-03-27 | 2018-10-24 | Japan Polyethylene Corporation | Polar-group-containing olefin copolymer, adhesive and layered product comprising same |
| CN103360544B (zh) * | 2013-07-26 | 2015-07-01 | 宁波工程学院 | 降冰片烯类、丙烯酸酯类和戊烯类共聚用催化剂及共聚方法 |
| CN111868064A (zh) * | 2017-10-31 | 2020-10-30 | 陶氏环球技术有限责任公司 | 包括碳硼烷助催化剂的催化剂体系 |
| CN113877551B (zh) * | 2021-10-25 | 2023-12-29 | 湖北科技学院 | 重金属和放射性金属离子吸附材料及其制备方法 |
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| KR20030005432A (ko) | 2000-05-31 | 2003-01-17 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 올레핀의 중합 |
| CN100369940C (zh) | 2000-05-31 | 2008-02-20 | 纳幕尔杜邦公司 | 烯烃聚合催化剂 |
| US20030144441A1 (en) | 2001-11-13 | 2003-07-31 | Ayusman Sen | Controlled copolymerization of methyl acrylate with olefins under mild conditions |
| US6730757B2 (en) | 2002-03-08 | 2004-05-04 | Exxonmobil Research And Engineering Company | Sulfur-containing and sulfur-nitrogen-containing catalysts for polymerization of olefins and polar monomers |
| WO2003102038A1 (en) | 2002-06-04 | 2003-12-11 | Thales Technologies, Ag | Polymerization catalysts |
| KR100576971B1 (ko) | 2002-09-13 | 2006-05-10 | 금호석유화학 주식회사 | 올레핀 중합용 이핵 전이금속 화합물의 제조 방법 |
| US6677419B1 (en) | 2002-11-13 | 2004-01-13 | International Business Machines Corporation | Preparation of copolymers |
| US7087687B2 (en) * | 2003-08-21 | 2006-08-08 | Rohm And Haas Company | Catalytic composition and its preparation and use for preparing polymers from ethylenically unsaturated monomers |
-
2004
- 2004-05-28 US US10/857,330 patent/US7087687B2/en not_active Expired - Fee Related
- 2004-08-07 EP EP04254775A patent/EP1508577A1/en not_active Withdrawn
- 2004-08-10 TW TW093123928A patent/TWI262196B/zh not_active IP Right Cessation
- 2004-08-20 CN CNB2004100641613A patent/CN1267460C/zh not_active Expired - Fee Related
- 2004-08-20 JP JP2004240323A patent/JP2005068424A/ja active Pending
- 2004-08-21 KR KR1020040066197A patent/KR100560061B1/ko not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| KR100560061B1 (ko) | 2006-03-13 |
| CN1597709A (zh) | 2005-03-23 |
| KR20050020725A (ko) | 2005-03-04 |
| TWI262196B (en) | 2006-09-21 |
| JP2005068424A (ja) | 2005-03-17 |
| US20050043494A1 (en) | 2005-02-24 |
| EP1508577A1 (en) | 2005-02-23 |
| TW200514795A (en) | 2005-05-01 |
| US7087687B2 (en) | 2006-08-08 |
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