KR20100137472A - 1-부텐 기재 중합체의 조성물 - Google Patents
1-부텐 기재 중합체의 조성물 Download PDFInfo
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- KR20100137472A KR20100137472A KR1020107020999A KR20107020999A KR20100137472A KR 20100137472 A KR20100137472 A KR 20100137472A KR 1020107020999 A KR1020107020999 A KR 1020107020999A KR 20107020999 A KR20107020999 A KR 20107020999A KR 20100137472 A KR20100137472 A KR 20100137472A
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- VXNZUUAINFGPBY-UHFFFAOYSA-N ethyl ethylene Natural products CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 title claims abstract description 97
- 239000000203 mixture Substances 0.000 title claims abstract description 42
- 229920000642 polymer Polymers 0.000 title claims abstract description 28
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 title description 3
- 229920001577 copolymer Polymers 0.000 claims abstract description 33
- 238000002844 melting Methods 0.000 claims abstract description 28
- 230000008018 melting Effects 0.000 claims abstract description 28
- 239000004711 α-olefin Substances 0.000 claims abstract description 24
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 claims abstract description 11
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000005977 Ethylene Substances 0.000 claims abstract description 9
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims abstract description 7
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims abstract description 7
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 claims abstract description 6
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 claims abstract description 5
- 238000005481 NMR spectroscopy Methods 0.000 claims abstract description 5
- 230000007704 transition Effects 0.000 claims abstract description 4
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 claims description 25
- 238000000034 method Methods 0.000 claims description 17
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims description 13
- 230000006835 compression Effects 0.000 claims description 7
- 238000007906 compression Methods 0.000 claims description 7
- 229920001519 homopolymer Polymers 0.000 claims description 5
- 235000012054 meals Nutrition 0.000 claims description 4
- 150000001336 alkenes Chemical class 0.000 claims description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 3
- 229920005606 polypropylene copolymer Polymers 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 description 24
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 21
- 238000006116 polymerization reaction Methods 0.000 description 21
- -1 alkyl radical Chemical class 0.000 description 19
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 18
- 239000003054 catalyst Substances 0.000 description 15
- 229910052757 nitrogen Inorganic materials 0.000 description 11
- 239000000243 solution Substances 0.000 description 11
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 10
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 10
- 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 10
- 229920006395 saturated elastomer Polymers 0.000 description 9
- AQZWEFBJYQSQEH-UHFFFAOYSA-N 2-methyloxaluminane Chemical compound C[Al]1CCCCO1 AQZWEFBJYQSQEH-UHFFFAOYSA-N 0.000 description 8
- 125000001424 substituent group Chemical group 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- 230000000737 periodic effect Effects 0.000 description 7
- 229910001220 stainless steel Inorganic materials 0.000 description 7
- 239000010935 stainless steel Substances 0.000 description 7
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 6
- 125000005842 heteroatom Chemical group 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 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 5
- ZMZGFLUUZLELNE-UHFFFAOYSA-N 2,3,5-triiodobenzoic acid Chemical compound OC(=O)C1=CC(I)=CC(I)=C1I ZMZGFLUUZLELNE-UHFFFAOYSA-N 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical group [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 4
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- 150000001450 anions Chemical class 0.000 description 4
- 150000001768 cations Chemical class 0.000 description 4
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 125000000538 pentafluorophenyl group Chemical group FC1=C(F)C(F)=C(*)C(F)=C1F 0.000 description 4
- 239000010959 steel Substances 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- 150000004645 aluminates Chemical class 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 235000010210 aluminium Nutrition 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical compound C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 description 3
- 125000005843 halogen group Chemical group 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000012299 nitrogen atmosphere Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000002076 thermal analysis method Methods 0.000 description 3
- SSEXLBWMXFFGTD-UHFFFAOYSA-N tris(2,3-dimethylbutyl)alumane Chemical compound CC(C)C(C)C[Al](CC(C)C(C)C)CC(C)C(C)C SSEXLBWMXFFGTD-UHFFFAOYSA-N 0.000 description 3
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical compound CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 2
- HNUALPPJLMYHDK-UHFFFAOYSA-N C[CH]C Chemical compound C[CH]C HNUALPPJLMYHDK-UHFFFAOYSA-N 0.000 description 2
- 229940126062 Compound A Drugs 0.000 description 2
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 2
- 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 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 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 group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 150000005840 aryl radicals Chemical class 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 2
- 150000001923 cyclic compounds Chemical class 0.000 description 2
- BOXSCYUXSBYGRD-UHFFFAOYSA-N cyclopenta-1,3-diene;iron(3+) Chemical compound [Fe+3].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 BOXSCYUXSBYGRD-UHFFFAOYSA-N 0.000 description 2
- 238000000113 differential scanning calorimetry Methods 0.000 description 2
- JLTDJTHDQAWBAV-UHFFFAOYSA-O dimethyl(phenyl)azanium Chemical compound C[NH+](C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-O 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 230000004927 fusion Effects 0.000 description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical group [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 239000010936 titanium Substances 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- IMFACGCPASFAPR-UHFFFAOYSA-O tributylazanium Chemical compound CCCC[NH+](CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-O 0.000 description 2
- MCULRUJILOGHCJ-UHFFFAOYSA-N triisobutylaluminium Chemical compound CC(C)C[Al](CC(C)C)CC(C)C MCULRUJILOGHCJ-UHFFFAOYSA-N 0.000 description 2
- JLTRXTDYQLMHGR-UHFFFAOYSA-N trimethylaluminium Chemical compound C[Al](C)C JLTRXTDYQLMHGR-UHFFFAOYSA-N 0.000 description 2
- HKVFGFGPRISDFM-UHFFFAOYSA-N tris(2,3,3-trimethylbutyl)alumane Chemical compound CC(C)(C)C(C)C[Al](CC(C)C(C)(C)C)CC(C)C(C)(C)C HKVFGFGPRISDFM-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 238000005406 washing Methods 0.000 description 2
- PHBVXHIVWULVNF-UHFFFAOYSA-N (4-fluorophenoxy)boronic acid Chemical compound OB(O)OC1=CC=C(F)C=C1 PHBVXHIVWULVNF-UHFFFAOYSA-N 0.000 description 1
- QPFMBZIOSGYJDE-QDNHWIQGSA-N 1,1,2,2-tetrachlorethane-d2 Chemical compound [2H]C(Cl)(Cl)C([2H])(Cl)Cl QPFMBZIOSGYJDE-QDNHWIQGSA-N 0.000 description 1
- UHWUPRFSWYYSEB-UHFFFAOYSA-N 1-[bis(2-trimethylsilylpropyl)alumanyl]propan-2-yl-trimethylsilane Chemical compound C[Si](C)(C)C(C)C[Al](CC(C)[Si](C)(C)C)CC(C)[Si](C)(C)C UHWUPRFSWYYSEB-UHFFFAOYSA-N 0.000 description 1
- KAESVJOAVNADME-UHFFFAOYSA-N 1H-pyrrole Natural products C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 1
- 229910018134 Al-Mg Inorganic materials 0.000 description 1
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- 229910018467 Al—Mg Inorganic materials 0.000 description 1
- 229910018520 Al—Si Inorganic materials 0.000 description 1
- 101100223811 Caenorhabditis elegans dsc-1 gene Proteins 0.000 description 1
- XBPCUCUWBYBCDP-UHFFFAOYSA-N Dicyclohexylamine Chemical compound C1CCCCC1NC1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-N 0.000 description 1
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- 238000004639 Schlenk technique Methods 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
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- HFKJQIJFRMRSKM-UHFFFAOYSA-N [3,5-bis(trifluoromethyl)phenoxy]boronic acid Chemical compound OB(O)OC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 HFKJQIJFRMRSKM-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
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- 125000001931 aliphatic group Chemical group 0.000 description 1
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- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- WXCZUWHSJWOTRV-UHFFFAOYSA-N but-1-ene;ethene Chemical group C=C.CCC=C WXCZUWHSJWOTRV-UHFFFAOYSA-N 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 238000007707 calorimetry Methods 0.000 description 1
- 238000001460 carbon-13 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000000254 composite pulse decoupling sequence Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
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- WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 description 1
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- 238000007429 general method Methods 0.000 description 1
- 229910052732 germanium Inorganic materials 0.000 description 1
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical group [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 239000001282 iso-butane Substances 0.000 description 1
- 229920001580 isotactic polymer Polymers 0.000 description 1
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- 238000011326 mechanical measurement Methods 0.000 description 1
- 239000013081 microcrystal Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
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- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 1
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- INNUJJCMHIUXQQ-UHFFFAOYSA-N tris(2,2-diphenylethyl)alumane Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)C[Al](CC(C=1C=CC=CC=1)C=1C=CC=CC=1)CC(C=1C=CC=CC=1)C1=CC=CC=C1 INNUJJCMHIUXQQ-UHFFFAOYSA-N 0.000 description 1
- PUGPVAUOXDRYSP-UHFFFAOYSA-N tris(2,3,3-trimethylhexyl)alumane Chemical compound CCCC(C)(C)C(C)C[Al](CC(C)C(C)(C)CCC)CC(C)C(C)(C)CCC PUGPVAUOXDRYSP-UHFFFAOYSA-N 0.000 description 1
- RXTYCDSTJDDMRJ-UHFFFAOYSA-N tris(2,3,3-trimethylpentyl)alumane Chemical compound CCC(C)(C)C(C)C[Al](CC(C)C(C)(C)CC)CC(C)C(C)(C)CC RXTYCDSTJDDMRJ-UHFFFAOYSA-N 0.000 description 1
- WRZKUDJYHWOMSC-UHFFFAOYSA-N tris(2,3-diethylpentyl)alumane Chemical compound CCC(CC)C(CC)C[Al](CC(CC)C(CC)CC)CC(CC)C(CC)CC WRZKUDJYHWOMSC-UHFFFAOYSA-N 0.000 description 1
- IBAAQZWRANCYLH-UHFFFAOYSA-N tris(2,3-dimethyl-3-phenylbutyl)alumane Chemical compound C=1C=CC=CC=1C(C)(C)C(C)C[Al](CC(C)C(C)(C)C=1C=CC=CC=1)CC(C)C(C)(C)C1=CC=CC=C1 IBAAQZWRANCYLH-UHFFFAOYSA-N 0.000 description 1
- WUGMXCQCNQHHDC-UHFFFAOYSA-N tris(2,3-dimethylheptyl)alumane Chemical compound CCCCC(C)C(C)C[Al](CC(C)C(C)CCCC)CC(C)C(C)CCCC WUGMXCQCNQHHDC-UHFFFAOYSA-N 0.000 description 1
- VGONMIOMLRCRSS-UHFFFAOYSA-N tris(2,3-dimethylhexyl)alumane Chemical compound CCCC(C)C(C)C[Al](CC(C)C(C)CCC)CC(C)C(C)CCC VGONMIOMLRCRSS-UHFFFAOYSA-N 0.000 description 1
- BENYMJNPVWYYES-UHFFFAOYSA-N tris(2,3-dimethylpentyl)alumane Chemical compound CCC(C)C(C)C[Al](CC(C)C(C)CC)CC(C)C(C)CC BENYMJNPVWYYES-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
- WXUZTGFTOYFKIR-UHFFFAOYSA-N tris(2-ethyl-3,3-dimethylbutyl)alumane Chemical compound CCC(C(C)(C)C)C[Al](CC(CC)C(C)(C)C)CC(CC)C(C)(C)C WXUZTGFTOYFKIR-UHFFFAOYSA-N 0.000 description 1
- IDEILWZYRDEEGQ-UHFFFAOYSA-N tris(2-ethyl-3,3-dimethylpentyl)alumane Chemical compound CCC(C)(C)C(CC)C[Al](CC(CC)C(C)(C)CC)CC(CC)C(C)(C)CC IDEILWZYRDEEGQ-UHFFFAOYSA-N 0.000 description 1
- FEJNOSHLGDRZDX-UHFFFAOYSA-N tris(2-ethyl-3-methylbutyl)alumane Chemical compound CCC(C(C)C)C[Al](CC(CC)C(C)C)CC(CC)C(C)C FEJNOSHLGDRZDX-UHFFFAOYSA-N 0.000 description 1
- JAFSWBPCWFKGBY-UHFFFAOYSA-N tris(2-ethyl-3-methylpentyl)alumane Chemical compound CCC(C)C(CC)C[Al](CC(CC)C(C)CC)CC(CC)C(C)CC JAFSWBPCWFKGBY-UHFFFAOYSA-N 0.000 description 1
- SHYOGCVYLVUSDK-UHFFFAOYSA-N tris(2-ethyl-3-phenylbutyl)alumane Chemical compound C=1C=CC=CC=1C(C)C(CC)C[Al](CC(CC)C(C)C=1C=CC=CC=1)CC(CC)C(C)C1=CC=CC=C1 SHYOGCVYLVUSDK-UHFFFAOYSA-N 0.000 description 1
- FVXNGHQGBIRVOB-UHFFFAOYSA-N tris(2-methyl-2-phenylpropyl)alumane Chemical compound C=1C=CC=CC=1C(C)(C)C[Al](CC(C)(C)C=1C=CC=CC=1)CC(C)(C)C1=CC=CC=C1 FVXNGHQGBIRVOB-UHFFFAOYSA-N 0.000 description 1
- ZMFQGYOUXPHLOA-UHFFFAOYSA-N tris(2-methyl-3-phenylbutyl)alumane Chemical compound C=1C=CC=CC=1C(C)C(C)C[Al](CC(C)C(C)C=1C=CC=CC=1)CC(C)C(C)C1=CC=CC=C1 ZMFQGYOUXPHLOA-UHFFFAOYSA-N 0.000 description 1
- JHKHTIUZAWUYBF-UHFFFAOYSA-N tris(2-methyl-3-propylhexyl)alumane Chemical compound CCCC(CCC)C(C)C[Al](CC(C)C(CCC)CCC)CC(C)C(CCC)CCC JHKHTIUZAWUYBF-UHFFFAOYSA-N 0.000 description 1
- ZOELJNRKNGBGAH-UHFFFAOYSA-N tris(2-phenylbutyl)alumane Chemical compound C=1C=CC=CC=1C(CC)C[Al](CC(CC)C=1C=CC=CC=1)CC(CC)C1=CC=CC=C1 ZOELJNRKNGBGAH-UHFFFAOYSA-N 0.000 description 1
- VFPYUYMFBROVAS-UHFFFAOYSA-N tris(2-phenylpentyl)alumane Chemical compound C=1C=CC=CC=1C(CCC)C[Al](CC(CCC)C=1C=CC=CC=1)CC(CCC)C1=CC=CC=C1 VFPYUYMFBROVAS-UHFFFAOYSA-N 0.000 description 1
- VJEKKLDXDUTOAK-UHFFFAOYSA-N tris(2-phenylpropyl)alumane Chemical compound C=1C=CC=CC=1C(C)C[Al](CC(C)C=1C=CC=CC=1)CC(C)C1=CC=CC=C1 VJEKKLDXDUTOAK-UHFFFAOYSA-N 0.000 description 1
- NEKKHOCWHFUARF-UHFFFAOYSA-N tris(2-propan-2-ylpentyl)alumane Chemical compound CCCC(C(C)C)C[Al](CC(CCC)C(C)C)CC(CCC)C(C)C NEKKHOCWHFUARF-UHFFFAOYSA-N 0.000 description 1
- NWZXKGHKCZTEHC-UHFFFAOYSA-N tris(3-ethyl-2-methylheptyl)alumane Chemical compound CCCCC(CC)C(C)C[Al](CC(C)C(CC)CCCC)CC(C)C(CC)CCCC NWZXKGHKCZTEHC-UHFFFAOYSA-N 0.000 description 1
- PZHDFOMROGHRBA-UHFFFAOYSA-N tris(3-ethyl-2-methylhexyl)alumane Chemical compound CCCC(CC)C(C)C[Al](CC(C)C(CC)CCC)CC(C)C(CC)CCC PZHDFOMROGHRBA-UHFFFAOYSA-N 0.000 description 1
- AMPVHNIRJXJXEN-UHFFFAOYSA-N tris(3-ethyl-2-methylpentyl)alumane Chemical compound CCC(CC)C(C)C[Al](CC(C)C(CC)CC)CC(C)C(CC)CC AMPVHNIRJXJXEN-UHFFFAOYSA-N 0.000 description 1
- QQRJKBIMCFKYOT-UHFFFAOYSA-N tris(3-methyl-2-phenylbutyl)alumane Chemical compound C=1C=CC=CC=1C(C(C)C)C[Al](CC(C(C)C)C=1C=CC=CC=1)CC(C(C)C)C1=CC=CC=C1 QQRJKBIMCFKYOT-UHFFFAOYSA-N 0.000 description 1
- VIDMRZMJMLMHSP-UHFFFAOYSA-N tris(3-methyl-2-propan-2-ylbutyl)alumane Chemical compound CC(C)C(C(C)C)C[Al](CC(C(C)C)C(C)C)CC(C(C)C)C(C)C VIDMRZMJMLMHSP-UHFFFAOYSA-N 0.000 description 1
- KFXLMHSDDUANFS-UHFFFAOYSA-N tris[2-(2,3,4,5,6-pentafluorophenyl)propyl]alumane Chemical compound FC=1C(F)=C(F)C(F)=C(F)C=1C(C)C[Al](CC(C)C=1C(=C(F)C(F)=C(F)C=1F)F)CC(C)C1=C(F)C(F)=C(F)C(F)=C1F KFXLMHSDDUANFS-UHFFFAOYSA-N 0.000 description 1
- JFJVQNAKPNAYCQ-UHFFFAOYSA-N tris[2-(3-propan-2-ylphenyl)propyl]alumane Chemical compound CC(C)C1=CC=CC(C(C)C[Al](CC(C)C=2C=C(C=CC=2)C(C)C)CC(C)C=2C=C(C=CC=2)C(C)C)=C1 JFJVQNAKPNAYCQ-UHFFFAOYSA-N 0.000 description 1
- ASSHEQWDGOTJRP-UHFFFAOYSA-N tris[2-(4-chlorophenyl)propyl]alumane Chemical compound C=1C=C(Cl)C=CC=1C(C)C[Al](CC(C)C=1C=CC(Cl)=CC=1)CC(C)C1=CC=C(Cl)C=C1 ASSHEQWDGOTJRP-UHFFFAOYSA-N 0.000 description 1
- ZCLZBCAKWSHDJL-UHFFFAOYSA-N tris[2-(4-fluorophenyl)propyl]alumane Chemical compound C=1C=C(F)C=CC=1C(C)C[Al](CC(C)C=1C=CC(F)=CC=1)CC(C)C1=CC=C(F)C=C1 ZCLZBCAKWSHDJL-UHFFFAOYSA-N 0.000 description 1
- 238000001969 wideband alternating-phase low-power technique for zero residual splitting Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 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
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/18—Homopolymers or copolymers of hydrocarbons having four or more carbon atoms
- C08L23/20—Homopolymers or copolymers of hydrocarbons having four or more carbon atoms having four to nine carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP08153149.3 | 2008-03-20 | ||
| EP08153149 | 2008-03-20 | ||
| US7205208P | 2008-03-27 | 2008-03-27 | |
| US61/072,052 | 2008-03-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20100137472A true KR20100137472A (ko) | 2010-12-30 |
Family
ID=40758999
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020107020999A Withdrawn KR20100137472A (ko) | 2008-03-20 | 2009-02-26 | 1-부텐 기재 중합체의 조성물 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US8097679B2 (https=) |
| EP (1) | EP2254946B1 (https=) |
| JP (1) | JP2011515518A (https=) |
| KR (1) | KR20100137472A (https=) |
| AT (1) | ATE543870T1 (https=) |
| BR (1) | BRPI0908997A2 (https=) |
| WO (1) | WO2009115400A1 (https=) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2254918A1 (en) * | 2008-03-20 | 2010-12-01 | Basell Poliolefine Italia S.R.L. | 1-butene terpolymers |
| US9200533B2 (en) | 2012-11-19 | 2015-12-01 | General Electric Company | Enthalpy determining apparatus, system and method |
| PT3266824T (pt) * | 2016-07-07 | 2022-04-06 | Basell Poliolefine Italia Srl | Composição polimérica de buteno-1 tendo um índice de fluidez elevado |
| PL3266825T3 (pl) | 2016-07-07 | 2022-05-09 | Basell Poliolefine Italia S.R.L. | Kompozycja polimerowa butenu-1 o wysokim wskaźniku szybkości płynięcia |
| JP7034252B2 (ja) * | 2017-08-04 | 2022-03-11 | バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ | 高い溶融流量を有するブテン－１重合体組成物 |
| EP3661972B1 (en) * | 2017-08-04 | 2024-03-27 | Basell Poliolefine Italia S.r.l. | Butene-1 polymer composition having high melt flow rate |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2254128C3 (de) * | 1972-11-04 | 1975-08-14 | Chemische Werke Huels Ag, 4370 Marl | Thermoplastische Formmasse aus Polybuten-I |
| DE2930108C2 (de) * | 1979-07-25 | 1982-11-25 | Chemische Werke Hüls AG, 4370 Marl | Verfahren zur Herstellung von weitgehend amorphen Buten-1 Propen-Ethen-Terpolymeren mit hohem Erweichungspunkt |
| DE3474673D1 (en) | 1984-08-30 | 1988-11-24 | Mitsui Petrochemical Ind | 1-butene polymer and its use |
| JPS61108614A (ja) | 1984-11-01 | 1986-05-27 | Mitsui Petrochem Ind Ltd | １−ブテン系ランダム共重合体 |
| US4642269A (en) | 1984-11-01 | 1987-02-10 | Mitsui Petrochemical Industries, Ltd | Crystalline random propylene copolymer composition and composite laminate comprising said composition |
| KR910005678B1 (ko) | 1987-07-20 | 1991-08-01 | 이데미쯔세끼유 가가꾸 가부시기가이샤 | 부텐-1 공중합체 |
| AU6158390A (en) | 1989-08-03 | 1991-03-11 | Exxon Chemical Patents Inc. | Very high molecular weight polyethylene |
| RU2118203C1 (ru) | 1990-06-22 | 1998-08-27 | Экксон Кэмикал Пейтентс Инк. | Каталитическая система для получения полиолефинов и композиция, используемая для полимеризации олефинов |
| JPH0477600A (ja) * | 1990-07-17 | 1992-03-11 | Sagami Chem Res Center | ドコサヘキサエン酸高含有脂質組成物の取得法 |
| US5221715A (en) * | 1990-09-21 | 1993-06-22 | Shell Oil Company | Poly(1-butene)resin composition |
| IT1264680B1 (it) * | 1993-07-07 | 1996-10-04 | Spherilene Srl | Catalizzatori supportati per la polimerizzazione delle olefine |
| IT1269837B (it) * | 1994-05-26 | 1997-04-15 | Spherilene Srl | Componenti e catalizzatori per la polimerizzazione delle olefine |
| JP3281389B2 (ja) * | 1995-06-08 | 2002-05-13 | 昭和電工株式会社 | イオン性化合物およびその化合物を用いたオレフィン重合用触媒 |
| US6559252B1 (en) * | 1997-10-29 | 2003-05-06 | Basell Technology Company Bv | Catalysts and processes for the polymerization of olefins |
| KR19990067851A (ko) * | 1998-01-14 | 1999-08-25 | 고오사이 아끼오 | 올레핀 중합체, 올레핀 중합 촉매 및 올레핀 중합체의 제조 방법 |
| EP0980396B2 (en) * | 1998-03-05 | 2009-08-19 | Basell Poliolefine Italia S.r.l. | Polybutene-1 (co)polymers and process for their preparation |
| DE19917985A1 (de) * | 1999-04-21 | 2000-10-26 | Targor Gmbh | Katalysatorsystem |
| BR0014616A (pt) * | 1999-09-22 | 2002-06-18 | Basell Technology Co Bv | Sistema catalìtico e processo para a polimerização de olefinas |
| DE19962910A1 (de) * | 1999-12-23 | 2001-07-05 | Targor Gmbh | Chemische Verbindung, Verfahren zu deren Herstellung und deren Verwendung in Katalysatorsystemen zur Herstellung von Polyolefinen |
| DE19962814A1 (de) * | 1999-12-23 | 2001-06-28 | Targor Gmbh | Neues Katalysatorsystem und dessen Verwendung |
| WO2001047939A1 (en) * | 1999-12-28 | 2001-07-05 | Basell Technology Company B.V. | Heterocyclic metallocene compounds and use thereof in catalyst systems for producing olefin polymers |
| WO2001062764A1 (en) | 2000-02-24 | 2001-08-30 | Basell Technology Company B.V. | Organometallic compound useful as cocatalyst for polymerizing olefins |
| KR100765398B1 (ko) * | 2000-07-03 | 2007-10-11 | 미쓰이 가가쿠 가부시키가이샤 | 부텐계 공중합체, 이 공중합체를 함유하는 수지 조성물,이 조성물의 성형체, 이 공중합체 제조용 고체상 티탄촉매 및 이 촉매의 제조 방법 |
| TWI263645B (en) * | 2000-08-22 | 2006-10-11 | Idemitsu Kosan Co | 1-butene based polymer and product formed therefrom |
| US6913834B2 (en) * | 2001-03-29 | 2005-07-05 | Idemitsu Kosan Co., Ltd. | Polyolefin resin composition, film, and multilayer structure |
| EP1446429B1 (en) * | 2001-06-12 | 2009-10-07 | Basell Polyolefine GmbH | Process for the polymerization of 1-butene |
| US7459511B2 (en) * | 2001-06-12 | 2008-12-02 | Basell Polyolefine Gmbh | Process for the polymerization of 1-butene |
| JP2005501841A (ja) * | 2001-08-01 | 2005-01-20 | バセル ポリオレフィン ジーエムビーエイチ | 複素環式ペンタレン誘導体の製造方法 |
| MY132768A (en) * | 2001-10-09 | 2007-10-31 | Basell Poliolefine Italia Spa | Crystalline propylene copolymer compositions having improved sealability and optical properties and reduced solubility. |
| EP1477499B1 (en) | 2002-02-21 | 2015-01-14 | Idemitsu Kosan Co., Ltd. | PROCESS FOR PRODUCING HIGH-FLuidity 1-BUTENE-based POLYMER |
| DE60309020T2 (de) * | 2002-05-29 | 2007-05-10 | Basell Poliolefine Italia S.R.L. | Buten-1-(co)polymere und verfahren zu ihrer herstellung |
| WO2004048424A1 (en) * | 2002-11-28 | 2004-06-10 | Basell Poliolefine Italia S.P.A. | Butene-1 copolymers and process for their preparation |
| AU2003296585A1 (en) | 2002-12-04 | 2004-06-23 | Basell Polyolefine Gmbh | 1-buten copolymers and process for preparing them |
| US7390862B2 (en) * | 2003-05-12 | 2008-06-24 | Basell Polyolefine Gmbh | Process for polymerizing 1-butene |
| WO2006005648A1 (en) * | 2004-07-13 | 2006-01-19 | Basell Polyolefine Gmbh | Metallocene compounds, ligands used in their preparation, preparation of 1-butene polymers and 1-butene polymers therefrom |
| PL1805231T3 (pl) * | 2004-10-18 | 2010-08-31 | Basell Poliolefine Italia Srl | (Ko)polimery butenu-1 o niskiej izotaktyczności |
| WO2006117285A1 (en) * | 2005-05-03 | 2006-11-09 | Basell Polyolefine Gmbh | Process for the polymerization of alpha olefins |
| DE112007002489T5 (de) | 2006-10-20 | 2009-09-10 | Idemitsu Kosan Co. Ltd. | Hochreines, endständig-ungesättigtes Olefinpolymer und Verfahren zur Herstellung davon |
| JP2008298998A (ja) * | 2007-05-30 | 2008-12-11 | Sony Corp | 映像表示装置 |
-
2009
- 2009-02-26 AT AT09721344T patent/ATE543870T1/de active
- 2009-02-26 BR BRPI0908997-7A patent/BRPI0908997A2/pt not_active IP Right Cessation
- 2009-02-26 JP JP2011500141A patent/JP2011515518A/ja active Pending
- 2009-02-26 WO PCT/EP2009/052274 patent/WO2009115400A1/en not_active Ceased
- 2009-02-26 US US12/735,953 patent/US8097679B2/en not_active Expired - Fee Related
- 2009-02-26 EP EP09721344A patent/EP2254946B1/en not_active Not-in-force
- 2009-02-26 KR KR1020107020999A patent/KR20100137472A/ko not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| US8097679B2 (en) | 2012-01-17 |
| EP2254946B1 (en) | 2012-02-01 |
| BRPI0908997A2 (pt) | 2015-08-04 |
| US20110003938A1 (en) | 2011-01-06 |
| EP2254946A1 (en) | 2010-12-01 |
| WO2009115400A1 (en) | 2009-09-24 |
| JP2011515518A (ja) | 2011-05-19 |
| ATE543870T1 (de) | 2012-02-15 |
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| PA0105 | International application |
Patent event date: 20100917 Patent event code: PA01051R01D Comment text: International Patent Application |
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| PG1501 | Laying open of application | ||
| PC1203 | Withdrawal of no request for examination | ||
| WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid |