SA03240450B1 - مكونات حفازة لبلمرة الاوليفينات - Google Patents
مكونات حفازة لبلمرة الاوليفينات Download PDFInfo
- Publication number
- SA03240450B1 SA03240450B1 SA03240450A SA03240450A SA03240450B1 SA 03240450 B1 SA03240450 B1 SA 03240450B1 SA 03240450 A SA03240450 A SA 03240450A SA 03240450 A SA03240450 A SA 03240450A SA 03240450 B1 SA03240450 B1 SA 03240450B1
- Authority
- SA
- Saudi Arabia
- Prior art keywords
- compound
- catalyst component
- solid catalyst
- component
- solid
- Prior art date
Links
- 239000003054 catalyst Substances 0.000 title claims abstract description 76
- 150000001336 alkenes Chemical class 0.000 title claims abstract description 19
- 238000006116 polymerization reaction Methods 0.000 title claims description 43
- 150000001875 compounds Chemical class 0.000 claims abstract description 81
- 238000000034 method Methods 0.000 claims abstract description 72
- 230000003197 catalytic effect Effects 0.000 claims abstract description 31
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 25
- 150000002170 ethers Chemical class 0.000 claims abstract description 14
- 150000002148 esters Chemical class 0.000 claims abstract description 12
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 12
- 150000002367 halogens Chemical class 0.000 claims abstract description 12
- 229920001577 copolymer Polymers 0.000 claims abstract description 11
- 229910052749 magnesium Inorganic materials 0.000 claims abstract description 10
- 150000002576 ketones Chemical class 0.000 claims abstract description 9
- 150000002825 nitriles Chemical class 0.000 claims abstract description 8
- 150000001412 amines Chemical class 0.000 claims abstract description 7
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical group C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 90
- 239000007787 solid Substances 0.000 claims description 53
- 239000010936 titanium Substances 0.000 claims description 43
- 239000011777 magnesium Substances 0.000 claims description 41
- 239000000203 mixture Substances 0.000 claims description 39
- -1 aliphatic ethers Chemical class 0.000 claims description 36
- 239000005977 Ethylene Substances 0.000 claims description 30
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 29
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 27
- 239000007788 liquid Substances 0.000 claims description 26
- 229920000642 polymer Polymers 0.000 claims description 25
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 22
- 239000011949 solid catalyst Substances 0.000 claims description 22
- 229910052739 hydrogen Inorganic materials 0.000 claims description 20
- 239000007789 gas Substances 0.000 claims description 14
- 229930195733 hydrocarbon Natural products 0.000 claims description 14
- 239000001257 hydrogen Substances 0.000 claims description 14
- 239000004215 Carbon black (E152) Substances 0.000 claims description 13
- 150000002430 hydrocarbons Chemical group 0.000 claims description 13
- 239000004711 α-olefin Substances 0.000 claims description 13
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- 229910052799 carbon Inorganic materials 0.000 claims description 11
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 9
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 7
- 125000005907 alkyl ester group Chemical group 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- 150000004292 cyclic ethers Chemical class 0.000 claims description 4
- 239000003085 diluting agent Substances 0.000 claims description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000004429 atom Chemical group 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 125000005842 heteroatom Chemical group 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- 229910052782 aluminium Inorganic materials 0.000 claims 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 4
- 229940126062 Compound A Drugs 0.000 claims 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims 1
- 150000001721 carbon Chemical group 0.000 claims 1
- 229940126214 compound 3 Drugs 0.000 claims 1
- 125000004981 cycloalkylmethyl group Chemical group 0.000 claims 1
- 238000002360 preparation method Methods 0.000 abstract description 21
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- 229920000092 linear low density polyethylene Polymers 0.000 abstract description 7
- 239000004707 linear low-density polyethylene Substances 0.000 abstract description 7
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 204
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 65
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 46
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 39
- 238000003756 stirring Methods 0.000 description 32
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- 229910052757 nitrogen Inorganic materials 0.000 description 20
- 239000012071 phase Substances 0.000 description 15
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 15
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 14
- 238000006243 chemical reaction Methods 0.000 description 13
- 239000000725 suspension Substances 0.000 description 13
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 12
- 239000000047 product Substances 0.000 description 12
- JLTRXTDYQLMHGR-UHFFFAOYSA-N trimethylaluminium Chemical compound C[Al](C)C JLTRXTDYQLMHGR-UHFFFAOYSA-N 0.000 description 12
- 239000000178 monomer Substances 0.000 description 11
- 239000001294 propane Substances 0.000 description 11
- 238000005406 washing Methods 0.000 description 11
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- YNLAOSYQHBDIKW-UHFFFAOYSA-M diethylaluminium chloride Chemical compound CC[Al](Cl)CC YNLAOSYQHBDIKW-UHFFFAOYSA-M 0.000 description 10
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- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 8
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- 239000000460 chlorine Substances 0.000 description 5
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- 238000013019 agitation Methods 0.000 description 4
- 125000001183 hydrocarbyl group Chemical group 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
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- YBJHBAHKTGYVGT-ZKWXMUAHSA-N biotin Natural products N1C(=O)N[C@@H]2[C@H](CCCCC(=O)O)SC[C@@H]21 YBJHBAHKTGYVGT-ZKWXMUAHSA-N 0.000 description 3
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 3
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- 229910001220 stainless steel Inorganic materials 0.000 description 3
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- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- DWKNOLCXIFYNFV-HSZRJFAPSA-N 2-[[(2r)-1-[1-[(4-chloro-3-methylphenyl)methyl]piperidin-4-yl]-5-oxopyrrolidine-2-carbonyl]amino]-n,n,6-trimethylpyridine-4-carboxamide Chemical compound CN(C)C(=O)C1=CC(C)=NC(NC(=O)[C@@H]2N(C(=O)CC2)C2CCN(CC=3C=C(C)C(Cl)=CC=3)CC2)=C1 DWKNOLCXIFYNFV-HSZRJFAPSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 101000787903 Homo sapiens Transmembrane protein 200C Proteins 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- 102100025939 Transmembrane protein 200C Human genes 0.000 description 2
- 238000002083 X-ray spectrum Methods 0.000 description 2
- YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 2
- 125000005234 alkyl aluminium group Chemical group 0.000 description 2
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 229960002685 biotin Drugs 0.000 description 2
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- 239000007795 chemical reaction product Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- JGHYBJVUQGTEEB-UHFFFAOYSA-M dimethylalumanylium;chloride Chemical compound C[Al](C)Cl JGHYBJVUQGTEEB-UHFFFAOYSA-M 0.000 description 2
- 150000004820 halides Chemical class 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
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- 238000002844 melting Methods 0.000 description 2
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- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 2
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- ITOFPJRDSCGOSA-KZLRUDJFSA-N (2s)-2-[[(4r)-4-[(3r,5r,8r,9s,10s,13r,14s,17r)-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-17-yl]pentanoyl]amino]-3-(1h-indol-3-yl)propanoic acid Chemical compound C([C@H]1CC2)[C@H](O)CC[C@]1(C)[C@@H](CC[C@]13C)[C@@H]2[C@@H]3CC[C@@H]1[C@H](C)CCC(=O)N[C@H](C(O)=O)CC1=CNC2=CC=CC=C12 ITOFPJRDSCGOSA-KZLRUDJFSA-N 0.000 description 1
- QFLWZFQWSBQYPS-AWRAUJHKSA-N (3S)-3-[[(2S)-2-[[(2S)-2-[5-[(3aS,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanoylamino]-3-methylbutanoyl]amino]-3-(4-hydroxyphenyl)propanoyl]amino]-4-[1-bis(4-chlorophenoxy)phosphorylbutylamino]-4-oxobutanoic acid Chemical compound CCCC(NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)CCCCC1SC[C@@H]2NC(=O)N[C@H]12)C(C)C)P(=O)(Oc1ccc(Cl)cc1)Oc1ccc(Cl)cc1 QFLWZFQWSBQYPS-AWRAUJHKSA-N 0.000 description 1
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- NYNZQNWKBKUAII-KBXCAEBGSA-N (3s)-n-[5-[(2r)-2-(2,5-difluorophenyl)pyrrolidin-1-yl]pyrazolo[1,5-a]pyrimidin-3-yl]-3-hydroxypyrrolidine-1-carboxamide Chemical compound C1[C@@H](O)CCN1C(=O)NC1=C2N=C(N3[C@H](CCC3)C=3C(=CC=C(F)C=3)F)C=CN2N=C1 NYNZQNWKBKUAII-KBXCAEBGSA-N 0.000 description 1
- UVGKQRAGAYVWQV-UHFFFAOYSA-N 2,3-dimethylbutan-2-yl(trimethoxy)silane Chemical group CO[Si](OC)(OC)C(C)(C)C(C)C UVGKQRAGAYVWQV-UHFFFAOYSA-N 0.000 description 1
- HFGHRUCCKVYFKL-UHFFFAOYSA-N 4-ethoxy-2-piperazin-1-yl-7-pyridin-4-yl-5h-pyrimido[5,4-b]indole Chemical compound C1=C2NC=3C(OCC)=NC(N4CCNCC4)=NC=3C2=CC=C1C1=CC=NC=C1 HFGHRUCCKVYFKL-UHFFFAOYSA-N 0.000 description 1
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- 108010021809 Alcohol dehydrogenase Proteins 0.000 description 1
- 241000726103 Atta Species 0.000 description 1
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- OOFLZRMKTMLSMH-UHFFFAOYSA-N H4atta Chemical compound OC(=O)CN(CC(O)=O)CC1=CC=CC(C=2N=C(C=C(C=2)C=2C3=CC=CC=C3C=C3C=CC=CC3=2)C=2N=C(CN(CC(O)=O)CC(O)=O)C=CC=2)=N1 OOFLZRMKTMLSMH-UHFFFAOYSA-N 0.000 description 1
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- DGEZNRSVGBDHLK-UHFFFAOYSA-N [1,10]phenanthroline Chemical compound C1=CN=C2C3=NC=CC=C3C=CC2=C1 DGEZNRSVGBDHLK-UHFFFAOYSA-N 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
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- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
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- SXPLZNMUBFBFIA-UHFFFAOYSA-N butyl(trimethoxy)silane Chemical compound CCCC[Si](OC)(OC)OC SXPLZNMUBFBFIA-UHFFFAOYSA-N 0.000 description 1
- 239000003426 co-catalyst Substances 0.000 description 1
- 229940125773 compound 10 Drugs 0.000 description 1
- 229940125810 compound 20 Drugs 0.000 description 1
- MEWFSXFFGFDHGV-UHFFFAOYSA-N cyclohexyl(trimethoxy)silane Chemical class CO[Si](OC)(OC)C1CCCCC1 MEWFSXFFGFDHGV-UHFFFAOYSA-N 0.000 description 1
- PDFVBOBULUSKAW-UHFFFAOYSA-N cyclohexyl-methoxy-dimethylsilane Chemical compound CO[Si](C)(C)C1CCCCC1 PDFVBOBULUSKAW-UHFFFAOYSA-N 0.000 description 1
- 238000009795 derivation Methods 0.000 description 1
- JWCYDYZLEAQGJJ-UHFFFAOYSA-N dicyclopentyl(dimethoxy)silane Chemical compound C1CCCC1[Si](OC)(OC)C1CCCC1 JWCYDYZLEAQGJJ-UHFFFAOYSA-N 0.000 description 1
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- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
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- 239000000706 filtrate Substances 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- JQOAQUXIUNVRQW-UHFFFAOYSA-N hexane Chemical compound CCCCCC.CCCCCC JQOAQUXIUNVRQW-UHFFFAOYSA-N 0.000 description 1
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- ZLVXBBHTMQJRSX-VMGNSXQWSA-N jdtic Chemical compound C1([C@]2(C)CCN(C[C@@H]2C)C[C@H](C(C)C)NC(=O)[C@@H]2NCC3=CC(O)=CC=C3C2)=CC=CC(O)=C1 ZLVXBBHTMQJRSX-VMGNSXQWSA-N 0.000 description 1
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- QMMOXUPEWRXHJS-UHFFFAOYSA-N pent-2-ene Chemical compound CCC=CC QMMOXUPEWRXHJS-UHFFFAOYSA-N 0.000 description 1
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- 238000012545 processing Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- ORYGRKHDLWYTKX-UHFFFAOYSA-N trihexylalumane Chemical compound CCCCCC[Al](CCCCCC)CCCCCC ORYGRKHDLWYTKX-UHFFFAOYSA-N 0.000 description 1
- LFXVBWRMVZPLFK-UHFFFAOYSA-N trioctylalumane Chemical compound CCCCCCCC[Al](CCCCCCCC)CCCCCCCC LFXVBWRMVZPLFK-UHFFFAOYSA-N 0.000 description 1
- XZIKSWMNFLIAQP-UHFFFAOYSA-N tris(2,4,4-trimethylpentyl)alumane Chemical compound CC(C)(C)CC(C)C[Al](CC(C)CC(C)(C)C)CC(C)CC(C)(C)C XZIKSWMNFLIAQP-UHFFFAOYSA-N 0.000 description 1
- 229920001862 ultra low molecular weight polyethylene Polymers 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
- 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
- C08F4/65—Pretreating the metal or compound covered by group C08F4/64 before the final contacting with the metal or compound covered by group C08F4/44
- C08F4/652—Pretreating with metals or metal-containing compounds
- C08F4/654—Pretreating with metals or metal-containing compounds with magnesium or compounds thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F10/02—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
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/16—Copolymers of ethene with alpha-alkenes, e.g. EP rubbers
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective 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)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP02080616 | 2002-12-18 | ||
| US43519502P | 2002-12-20 | 2002-12-20 |
Publications (1)
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| SA03240450B1 true SA03240450B1 (ar) | 2009-01-19 |
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ID=35925132
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
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| SA03240450A SA03240450B1 (ar) | 2002-12-18 | 2003-12-20 | مكونات حفازة لبلمرة الاوليفينات |
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| JP (2) | JP2006510751A (enExample) |
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| BR (1) | BR0316913B1 (enExample) |
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| ES (2) | ES2420879T3 (enExample) |
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| RU (1) | RU2322457C2 (enExample) |
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| TW (1) | TW200417554A (enExample) |
| WO (1) | WO2004055065A1 (enExample) |
| ZA (2) | ZA200504127B (enExample) |
Families Citing this family (44)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2527357A1 (en) * | 2003-05-29 | 2004-12-09 | Basell Poliolefine Italia S.R.L. | Process for the preparation of a catalyst component and components therefrom obtained |
| EP1780225A1 (en) | 2005-11-01 | 2007-05-02 | Borealis Technology Oy | Ziegler-Natta catalyst and its use to prepare multimodal polyolefin |
| BRPI0709454B8 (pt) * | 2006-04-06 | 2018-02-27 | Beijing Res Inst Chemical Ind China Petroleum & Chemical Corp | complexo de haleto de magnésio, processo para preparar o complexo de olefínica, catalisador para a polimerização de uma olefina e processo para polimerizar olefinas |
| CN101165074B (zh) * | 2006-10-20 | 2010-12-22 | 中国石油化工股份有限公司 | 用于烯烃聚合的催化剂组分及其催化剂 |
| CN101486776B (zh) * | 2008-01-17 | 2010-12-22 | 中国石油化工股份有限公司 | 用于烯烃聚合的催化剂组分及其催化剂 |
| RU2493175C2 (ru) * | 2008-09-26 | 2013-09-20 | Базелль Полиолефин Италия С.Р.Л. | Каталитические компоненты для полимеризации олефинов |
| RU2567391C2 (ru) | 2009-08-21 | 2015-11-10 | Чайна Петролеум Энд Кемикал Корпорейшн | Компонент катализатора для полимеризации этилена, приготовление такового и катализатор, включающий компонент катализатора |
| SA3686B1 (ar) | 2009-10-16 | 2014-10-22 | China Petroleum& Chemical Corp | مكون حفاز لبلمرة الأولفين وحفاز يشتمل عليه |
| US20110319571A1 (en) * | 2010-06-29 | 2011-12-29 | Botros Maged G | Polyolefin adhesive composition |
| US10138310B2 (en) * | 2010-08-24 | 2018-11-27 | Equistar Chemicals, Lp | Preparation of LLDPE resins and films having low gels |
| RU2579371C2 (ru) * | 2010-08-24 | 2016-04-10 | Базелль Полиолефин Италия С.Р.Л. | Компоненты катализатора для полимеризации олефинов |
| US20120053305A1 (en) * | 2010-08-24 | 2012-03-01 | Equistar Chemicals, Lp | Preparation of LLDPE having controlled xylene solubles or hexane extractables |
| RU2584694C2 (ru) * | 2010-09-28 | 2016-05-20 | Базелль Полиолефине Гмбх | Полиэтиленовые экструдированные изделия |
| CN103119072B (zh) * | 2010-09-30 | 2016-03-30 | 巴塞尔聚烯烃意大利有限责任公司 | 二氯化镁-醇加合物和由其获得的催化剂组分 |
| CN102585056A (zh) * | 2011-01-05 | 2012-07-18 | 中国石油化工股份有限公司 | 一种用于乙烯聚合或共聚合反应的催化剂 |
| EP2610273B1 (en) * | 2011-12-30 | 2018-02-07 | Borealis AG | Catalyst component |
| EP2692743A1 (en) | 2012-08-03 | 2014-02-05 | Basell Poliolefine Italia S.r.l. | Magnesium dichloride-alcohol adducts and catalyst components obtained therefrom |
| EP2712875A1 (en) | 2012-09-28 | 2014-04-02 | Basell Poliolefine Italia S.r.l. | Catalyst components for the polymerization of olefins |
| CN103788246B (zh) * | 2012-10-29 | 2015-10-21 | 中国石油化工股份有限公司 | 一种烯烃聚合催化剂载体及其制备方法和应用 |
| CN104981487B (zh) * | 2013-01-31 | 2017-03-08 | 沙特基础工业公司 | 用于烯烃聚合的催化剂组合物 |
| KR102100006B1 (ko) * | 2013-02-27 | 2020-05-26 | 도호 티타늄 가부시키가이샤 | 프로필렌계 블록 공중합체의 제조 방법 |
| CN104231140B (zh) * | 2013-06-21 | 2016-12-07 | 中国石油天然气集团公司 | 一种乙烯-α-烯烃共聚催化剂及其制备和应用 |
| WO2015012963A1 (en) * | 2013-07-25 | 2015-01-29 | Exxonmobil Chemical Patents Inc. | Methods for polyolefin polymerization with high activity catalyst systems |
| FI3116921T3 (fi) * | 2014-03-14 | 2024-02-14 | Basell Poliolefine Italia Srl | Katalyyttikomponentteja olefiinien polymerointiin |
| FR3023183A1 (fr) * | 2014-07-04 | 2016-01-08 | IFP Energies Nouvelles | Composition catalytique et procede de dimerisation selective de l'ethylene en butene-1 |
| CA2970848C (en) | 2014-12-18 | 2023-04-11 | Borealis Ag | Ziegler-natta catalyst and preparation thereof |
| CN112979842B (zh) | 2015-02-05 | 2022-11-11 | 博里利斯股份公司 | 用于生产聚乙烯的方法 |
| WO2017042058A1 (en) * | 2015-09-11 | 2017-03-16 | Basell Poliolefine Italia S.R.L. | Process for the preparation of catalyst components for the polymerization of olefins |
| BR112019000090A2 (pt) | 2016-07-15 | 2019-04-09 | Basell Poliolefine Italia Srl | catalisador para a polimerização de olefinas |
| BR112019011717B1 (pt) * | 2016-12-19 | 2022-11-01 | Basell Poliolefine Italia S.R.L. | Componente catalisador para a polimerização de olefinas, catalisadores obtidos a partir dos mesmos e processo para a (co)polimerização de olefinas |
| EP3339333B1 (en) | 2016-12-22 | 2020-10-07 | Borealis AG | Ziegler-natta catalyst and preparation thereof |
| BR112020001201B1 (pt) | 2017-07-19 | 2023-03-21 | Beijing Research Institute Of Chemical Industry, China Petroleum & Chemical Corporation | Sistema catalisador ziegler-natta para polimerização olefínica, componente catalisador sólido para polimerização olefínica e processo de polimerização olefínica |
| SG11202005004UA (en) * | 2017-12-05 | 2020-06-29 | Univation Tech Llc | Activated spray-dried ziegler-natta catalyst system |
| SG11202004922SA (en) | 2017-12-05 | 2020-06-29 | Univation Tech Llc | Modified spray-dried ziegler-natta (pro)catalyst systems |
| EP3732208A1 (en) | 2017-12-27 | 2020-11-04 | Borealis AG | Ziegler-natta catalyst and preparation thereof |
| CA3086639A1 (en) | 2017-12-28 | 2019-07-04 | Borealis Ag | Catalyst and preparation thereof |
| WO2019231815A1 (en) * | 2018-06-01 | 2019-12-05 | Dow Global Technologies Llc | Ziegler-natta catalyst system having a thermally treated magnesium chloride component |
| CN114585654B (zh) | 2019-10-04 | 2023-11-07 | 北欧化工公司 | 用于烯烃聚合的齐格勒-纳塔催化剂 |
| WO2021064083A1 (en) | 2019-10-04 | 2021-04-08 | Borealis Ag | Ziegler-natta catalysts for olefin polymerization |
| EP4038110B1 (en) | 2019-10-04 | 2026-01-21 | Borealis GmbH | Ziegler-natta catalysts for olefin polymerization |
| CN114466872B (zh) | 2019-10-04 | 2024-01-30 | 北欧化工公司 | 用于烯烃聚合的齐格勒纳塔催化剂 |
| CN112812205B (zh) * | 2019-11-18 | 2023-05-09 | 中国石油化工股份有限公司 | 一种用于烯烃聚合反应的催化剂组分及其催化剂和其制法及应用 |
| EP4143241A1 (en) | 2020-04-30 | 2023-03-08 | Dow Global Technologies LLC | Ziegler-natta (pro)catalyst systems made with (multi-alkoxy)silane compound |
| WO2022089423A1 (zh) * | 2020-10-26 | 2022-05-05 | 中国石油化工股份有限公司 | 用于制备烯烃聚合催化剂的固体组分及其制备方法和应用 |
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| BR9405129A (pt) * | 1993-12-17 | 1995-08-22 | Union Carbide Chem Plastic | Sistema catalisador;processo para a polimerzação de etileno;processo para a produção de uma composição de tricloreto de titânio |
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| JP3895050B2 (ja) * | 1997-08-11 | 2007-03-22 | 三井化学株式会社 | 固体状チタン触媒成分の調製方法 |
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-
2003
- 2003-11-25 BR BRPI0316913-8A patent/BR0316913B1/pt active IP Right Grant
- 2003-11-25 CA CA2510679A patent/CA2510679C/en not_active Expired - Lifetime
- 2003-11-25 AU AU2003292199A patent/AU2003292199A1/en not_active Abandoned
- 2003-11-25 ES ES03767757T patent/ES2420879T3/es not_active Expired - Lifetime
- 2003-11-25 US US10/537,077 patent/US7427653B2/en not_active Expired - Lifetime
- 2003-11-25 RU RU2005122489/04A patent/RU2322457C2/ru active
- 2003-11-25 EP EP03767757.2A patent/EP1572756B1/en not_active Revoked
- 2003-11-25 MX MXPA05006584A patent/MXPA05006584A/es unknown
- 2003-11-25 WO PCT/EP2003/013807 patent/WO2004055065A1/en not_active Ceased
- 2003-11-25 CN CNA200380106191XA patent/CN1726080A/zh active Pending
- 2003-11-25 KR KR1020057011380A patent/KR101102793B1/ko not_active Expired - Lifetime
- 2003-11-25 ES ES03789154T patent/ES2368425T3/es not_active Expired - Lifetime
- 2003-11-25 CN CNB2003801061943A patent/CN100554287C/zh not_active Expired - Lifetime
- 2003-11-25 JP JP2004559767A patent/JP2006510751A/ja not_active Withdrawn
- 2003-12-10 TW TW092134831A patent/TW200417554A/zh unknown
- 2003-12-17 AR ARP030104667A patent/AR042496A1/es unknown
- 2003-12-20 SA SA03240450A patent/SA03240450B1/ar unknown
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2005
- 2005-05-20 ZA ZA200504127A patent/ZA200504127B/en unknown
- 2005-05-20 ZA ZA200504131A patent/ZA200504131B/en unknown
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2010
- 2010-07-30 JP JP2010172060A patent/JP5366898B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| BR0316913B1 (pt) | 2014-09-09 |
| ZA200504127B (en) | 2006-02-22 |
| TW200417554A (en) | 2004-09-16 |
| CA2510679A1 (en) | 2004-07-01 |
| ES2368425T3 (es) | 2011-11-17 |
| CN1726230A (zh) | 2006-01-25 |
| RU2322457C2 (ru) | 2008-04-20 |
| RU2005122489A (ru) | 2006-01-20 |
| ES2420879T3 (es) | 2013-08-27 |
| KR101102793B1 (ko) | 2012-01-05 |
| ZA200504131B (en) | 2006-02-22 |
| BR0316913A (pt) | 2005-10-18 |
| AU2003292199A1 (en) | 2004-07-09 |
| WO2004055065A1 (en) | 2004-07-01 |
| CN100554287C (zh) | 2009-10-28 |
| JP2006510751A (ja) | 2006-03-30 |
| AR042496A1 (es) | 2005-06-22 |
| JP5366898B2 (ja) | 2013-12-11 |
| JP2010280894A (ja) | 2010-12-16 |
| EP1572756A1 (en) | 2005-09-14 |
| EP1572756B1 (en) | 2013-04-10 |
| MXPA05006584A (es) | 2005-08-16 |
| US7427653B2 (en) | 2008-09-23 |
| CN1726080A (zh) | 2006-01-25 |
| KR20050084415A (ko) | 2005-08-26 |
| CA2510679C (en) | 2013-04-23 |
| US20060089251A1 (en) | 2006-04-27 |
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