SG183028A1 - Ethylene/a-olefin interpolymers containing low crystallinity hard blocks - Google Patents
Ethylene/a-olefin interpolymers containing low crystallinity hard blocks Download PDFInfo
- Publication number
- SG183028A1 SG183028A1 SG2012052015A SG2012052015A SG183028A1 SG 183028 A1 SG183028 A1 SG 183028A1 SG 2012052015 A SG2012052015 A SG 2012052015A SG 2012052015 A SG2012052015 A SG 2012052015A SG 183028 A1 SG183028 A1 SG 183028A1
- Authority
- SG
- Singapore
- Prior art keywords
- ethylene
- polymer
- olefin interpolymer
- olefin
- interpolymer
- Prior art date
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- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 title claims abstract description 167
- 239000005977 Ethylene Substances 0.000 title claims abstract description 167
- 229920001577 copolymer Polymers 0.000 claims abstract description 24
- 229920000642 polymer Polymers 0.000 claims description 167
- 239000000203 mixture Substances 0.000 claims description 61
- 239000000178 monomer Substances 0.000 claims description 36
- 238000009826 distribution Methods 0.000 claims description 25
- 238000002844 melting Methods 0.000 claims description 20
- 230000008018 melting Effects 0.000 claims description 20
- 229910052799 carbon Inorganic materials 0.000 claims description 19
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims description 16
- 238000005259 measurement Methods 0.000 claims description 15
- 239000000155 melt Substances 0.000 claims description 13
- 229920005604 random copolymer Polymers 0.000 claims description 10
- 229910052775 Thulium Inorganic materials 0.000 claims description 4
- 239000004711 α-olefin Substances 0.000 abstract description 7
- 239000003054 catalyst Substances 0.000 description 50
- 238000000034 method Methods 0.000 description 36
- 229920001400 block copolymer Polymers 0.000 description 33
- -1 I-octene Chemical compound 0.000 description 25
- 150000001993 dienes Chemical class 0.000 description 24
- 239000000243 solution Substances 0.000 description 23
- 239000002904 solvent Substances 0.000 description 18
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 17
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 17
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 17
- 239000003921 oil Substances 0.000 description 16
- 150000001336 alkenes Chemical class 0.000 description 15
- 238000005481 NMR spectroscopy Methods 0.000 description 14
- 239000003795 chemical substances by application Substances 0.000 description 14
- 238000000113 differential scanning calorimetry Methods 0.000 description 14
- 238000006116 polymerization reaction Methods 0.000 description 14
- 239000000126 substance Chemical group 0.000 description 13
- 230000004044 response Effects 0.000 description 12
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 11
- 238000005227 gel permeation chromatography Methods 0.000 description 11
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- 230000000052 comparative effect Effects 0.000 description 10
- SOEVKJXMZBAALG-UHFFFAOYSA-N octylalumane Chemical compound CCCCCCCC[AlH2] SOEVKJXMZBAALG-UHFFFAOYSA-N 0.000 description 10
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 9
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 238000005194 fractionation Methods 0.000 description 9
- 230000008569 process Effects 0.000 description 9
- 239000000523 sample Substances 0.000 description 9
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 8
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 8
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 8
- 238000004364 calculation method Methods 0.000 description 8
- 125000000524 functional group Chemical group 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 7
- 229920001971 elastomer Polymers 0.000 description 7
- 238000010828 elution Methods 0.000 description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- OJOWICOBYCXEKR-APPZFPTMSA-N (1S,4R)-5-ethylidenebicyclo[2.2.1]hept-2-ene Chemical compound CC=C1C[C@@H]2C[C@@H]1C=C2 OJOWICOBYCXEKR-APPZFPTMSA-N 0.000 description 6
- XWJBRBSPAODJER-UHFFFAOYSA-N 1,7-octadiene Chemical compound C=CCCCCC=C XWJBRBSPAODJER-UHFFFAOYSA-N 0.000 description 6
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 6
- HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical compound C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 6
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 235000015107 ale Nutrition 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 description 6
- 239000000806 elastomer Substances 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- 238000010348 incorporation Methods 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical class CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- PRBHEGAFLDMLAL-GQCTYLIASA-N (4e)-hexa-1,4-diene Chemical compound C\C=C\CC=C PRBHEGAFLDMLAL-GQCTYLIASA-N 0.000 description 5
- 239000004793 Polystyrene Substances 0.000 description 5
- 238000011088 calibration curve Methods 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 5
- 230000000704 physical effect Effects 0.000 description 5
- 229920000573 polyethylene Polymers 0.000 description 5
- 229920000098 polyolefin Polymers 0.000 description 5
- WTQBISBWKRKLIJ-UHFFFAOYSA-N 5-methylidenebicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(=C)CC1C=C2 WTQBISBWKRKLIJ-UHFFFAOYSA-N 0.000 description 4
- 238000004566 IR spectroscopy Methods 0.000 description 4
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 4
- 229920002223 polystyrene Polymers 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- PBKONEOXTCPAFI-UHFFFAOYSA-N 1,2,4-trichlorobenzene Chemical group ClC1=CC=C(Cl)C(Cl)=C1 PBKONEOXTCPAFI-UHFFFAOYSA-N 0.000 description 3
- 229920002943 EPDM rubber Polymers 0.000 description 3
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- HQWPLXHWEZZGKY-UHFFFAOYSA-N diethylzinc Chemical compound CC[Zn]CC HQWPLXHWEZZGKY-UHFFFAOYSA-N 0.000 description 3
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 3
- MGDOJPNDRJNJBK-UHFFFAOYSA-N ethylaluminum Chemical compound [Al].C[CH2] MGDOJPNDRJNJBK-UHFFFAOYSA-N 0.000 description 3
- 229920001038 ethylene copolymer Polymers 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 239000006260 foam Substances 0.000 description 3
- 229920001519 homopolymer Polymers 0.000 description 3
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 3
- SJYNFBVQFBRSIB-UHFFFAOYSA-N norbornadiene Chemical compound C1=CC2C=CC1C2 SJYNFBVQFBRSIB-UHFFFAOYSA-N 0.000 description 3
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 3
- 230000000379 polymerizing effect Effects 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 229920001187 thermosetting polymer Polymers 0.000 description 3
- 239000003039 volatile agent Substances 0.000 description 3
- 229910052726 zirconium Inorganic materials 0.000 description 3
- PRBHEGAFLDMLAL-UHFFFAOYSA-N 1,5-Hexadiene Natural products CC=CCC=C PRBHEGAFLDMLAL-UHFFFAOYSA-N 0.000 description 2
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N 1-Heptene Chemical compound CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 2
- RYPKRALMXUUNKS-UHFFFAOYSA-N 2-Hexene Natural products CCCC=CC RYPKRALMXUUNKS-UHFFFAOYSA-N 0.000 description 2
- FUDNBFMOXDUIIE-UHFFFAOYSA-N 3,7-dimethylocta-1,6-diene Chemical compound C=CC(C)CCC=C(C)C FUDNBFMOXDUIIE-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- 239000004322 Butylated hydroxytoluene Substances 0.000 description 2
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 2
- YEYLJURTFOLIQG-UHFFFAOYSA-N CCCCCC[Zn] Chemical compound CCCCCC[Zn] YEYLJURTFOLIQG-UHFFFAOYSA-N 0.000 description 2
- VCFQUHAHCQJWKL-UHFFFAOYSA-N CC[Zn+].CC(C)(C)[O-] Chemical compound CC[Zn+].CC(C)(C)[O-] VCFQUHAHCQJWKL-UHFFFAOYSA-N 0.000 description 2
- RDRSMXYUSKJLIZ-UHFFFAOYSA-M CC[Zn+].[O-]C1=C(C=2C=CC=CC=2)C=CC=C1C1=CC=CC=C1 Chemical compound CC[Zn+].[O-]C1=C(C=2C=CC=CC=2)C=CC=C1C1=CC=CC=C1 RDRSMXYUSKJLIZ-UHFFFAOYSA-M 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000004609 Impact Modifier Substances 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000008186 active pharmaceutical agent Substances 0.000 description 2
- 150000001335 aliphatic alkanes Chemical class 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 239000012267 brine Substances 0.000 description 2
- 229940095259 butylated hydroxytoluene Drugs 0.000 description 2
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- MGNZXYYWBUKAII-UHFFFAOYSA-N cyclohexa-1,3-diene Chemical compound C1CC=CC=C1 MGNZXYYWBUKAII-UHFFFAOYSA-N 0.000 description 2
- URYYVOIYTNXXBN-UPHRSURJSA-N cyclooctene Chemical compound C1CCC\C=C/CC1 URYYVOIYTNXXBN-UPHRSURJSA-N 0.000 description 2
- 239000004913 cyclooctene Substances 0.000 description 2
- NLDGJRWPPOSWLC-UHFFFAOYSA-N deca-1,9-diene Chemical compound C=CCCCCCCC=C NLDGJRWPPOSWLC-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 2
- 230000004927 fusion Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 229910052735 hafnium Inorganic materials 0.000 description 2
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical compound C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 2
- DPUXQWOMYBMHRN-UHFFFAOYSA-N hexa-2,3-diene Chemical compound CCC=C=CC DPUXQWOMYBMHRN-UHFFFAOYSA-N 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- 230000000977 initiatory effect Effects 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 230000010354 integration Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 2
- CCCMONHAUSKTEQ-UHFFFAOYSA-N octadec-1-ene Chemical compound CCCCCCCCCCCCCCCCC=C CCCMONHAUSKTEQ-UHFFFAOYSA-N 0.000 description 2
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- 239000002685 polymerization catalyst Substances 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000010926 purge Methods 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 230000000630 rising effect Effects 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 229920001897 terpolymer Polymers 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- LFXVBWRMVZPLFK-UHFFFAOYSA-N trioctylalumane Chemical compound CCCCCCCC[Al](CCCCCCCC)CCCCCCCC LFXVBWRMVZPLFK-UHFFFAOYSA-N 0.000 description 2
- KEMUGHMYINTXKW-NQOXHWNZSA-N (1z,5z)-cyclododeca-1,5-diene Chemical compound C1CCC\C=C/CC\C=C/CC1 KEMUGHMYINTXKW-NQOXHWNZSA-N 0.000 description 1
- OJOWICOBYCXEKR-KRXBUXKQSA-N (5e)-5-ethylidenebicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(=C/C)/CC1C=C2 OJOWICOBYCXEKR-KRXBUXKQSA-N 0.000 description 1
- RJUCIROUEDJQIB-GQCTYLIASA-N (6e)-octa-1,6-diene Chemical compound C\C=C\CCCC=C RJUCIROUEDJQIB-GQCTYLIASA-N 0.000 description 1
- 125000006659 (C1-C20) hydrocarbyl group Chemical group 0.000 description 1
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical compound C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 description 1
- QPFMBZIOSGYJDE-MICDWDOJSA-N 1,1,2,2-tetrachloro-1-deuterioethane Chemical compound [2H]C(Cl)(Cl)C(Cl)Cl QPFMBZIOSGYJDE-MICDWDOJSA-N 0.000 description 1
- QWUWMCYKGHVNAV-UHFFFAOYSA-N 1,2-dihydrostilbene Chemical group C=1C=CC=CC=1CCC1=CC=CC=C1 QWUWMCYKGHVNAV-UHFFFAOYSA-N 0.000 description 1
- VYXHVRARDIDEHS-UHFFFAOYSA-N 1,5-cyclooctadiene Chemical compound C1CC=CCCC=C1 VYXHVRARDIDEHS-UHFFFAOYSA-N 0.000 description 1
- 239000004912 1,5-cyclooctadiene Substances 0.000 description 1
- NVZWEEGUWXZOKI-UHFFFAOYSA-N 1-ethenyl-2-methylbenzene Chemical compound CC1=CC=CC=C1C=C NVZWEEGUWXZOKI-UHFFFAOYSA-N 0.000 description 1
- PPWUTZVGSFPZOC-UHFFFAOYSA-N 1-methyl-2,3,3a,4-tetrahydro-1h-indene Chemical compound C1C=CC=C2C(C)CCC21 PPWUTZVGSFPZOC-UHFFFAOYSA-N 0.000 description 1
- DKCPKDPYUFEZCP-UHFFFAOYSA-N 2,6-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=CC(C(C)(C)C)=C1O DKCPKDPYUFEZCP-UHFFFAOYSA-N 0.000 description 1
- YXRZFCBXBJIBAP-UHFFFAOYSA-N 2,6-dimethylocta-1,7-diene Chemical compound C=CC(C)CCCC(C)=C YXRZFCBXBJIBAP-UHFFFAOYSA-N 0.000 description 1
- AQZWEFBJYQSQEH-UHFFFAOYSA-N 2-methyloxaluminane Chemical class C[Al]1CCCCO1 AQZWEFBJYQSQEH-UHFFFAOYSA-N 0.000 description 1
- MHGWNYIERCEISS-UHFFFAOYSA-N 2-methylpropyl(dioctadecyl)alumane Chemical compound CCCCCCCCCCCCCCCCCC[Al](CC(C)C)CCCCCCCCCCCCCCCCCC MHGWNYIERCEISS-UHFFFAOYSA-N 0.000 description 1
- YUFQUBWPYIPRHZ-UHFFFAOYSA-N 2-n,3-n-bis[2,6-di(propan-2-yl)phenyl]butane-2,3-diimine Chemical compound CC(C)C1=CC=CC(C(C)C)=C1N=C(C)C(C)=NC1=C(C(C)C)C=CC=C1C(C)C YUFQUBWPYIPRHZ-UHFFFAOYSA-N 0.000 description 1
- WJQOZHYUIDYNHM-UHFFFAOYSA-N 2-tert-Butylphenol Chemical compound CC(C)(C)C1=CC=CC=C1O WJQOZHYUIDYNHM-UHFFFAOYSA-N 0.000 description 1
- DXIJHCSGLOHNES-UHFFFAOYSA-N 3,3-dimethylbut-1-enylbenzene Chemical compound CC(C)(C)C=CC1=CC=CC=C1 DXIJHCSGLOHNES-UHFFFAOYSA-N 0.000 description 1
- KPYCVQASEGGKEG-UHFFFAOYSA-N 3-hydroxyoxolane-2,5-dione Chemical compound OC1CC(=O)OC1=O KPYCVQASEGGKEG-UHFFFAOYSA-N 0.000 description 1
- YHQXBTXEYZIYOV-UHFFFAOYSA-N 3-methylbut-1-ene Chemical compound CC(C)C=C YHQXBTXEYZIYOV-UHFFFAOYSA-N 0.000 description 1
- LDTAOIUHUHHCMU-UHFFFAOYSA-N 3-methylpent-1-ene Chemical compound CCC(C)C=C LDTAOIUHUHHCMU-UHFFFAOYSA-N 0.000 description 1
- UFERIGCCDYCZLN-UHFFFAOYSA-N 3a,4,7,7a-tetrahydro-1h-indene Chemical compound C1C=CCC2CC=CC21 UFERIGCCDYCZLN-UHFFFAOYSA-N 0.000 description 1
- FSWNZCWHTXTQBY-UHFFFAOYSA-N 4,6-dimethylhept-1-ene Chemical compound CC(C)CC(C)CC=C FSWNZCWHTXTQBY-UHFFFAOYSA-N 0.000 description 1
- BBDKZWKEPDTENS-UHFFFAOYSA-N 4-Vinylcyclohexene Chemical compound C=CC1CCC=CC1 BBDKZWKEPDTENS-UHFFFAOYSA-N 0.000 description 1
- NWPQAENAYWENSD-UHFFFAOYSA-N 5-butylidenebicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(=CCCC)CC1C=C2 NWPQAENAYWENSD-UHFFFAOYSA-N 0.000 description 1
- INYHZQLKOKTDAI-UHFFFAOYSA-N 5-ethenylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(C=C)CC1C=C2 INYHZQLKOKTDAI-UHFFFAOYSA-N 0.000 description 1
- KLAWFKRMCIXRFS-UHFFFAOYSA-N 5-ethenylidenebicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(=C=C)CC1C=C2 KLAWFKRMCIXRFS-UHFFFAOYSA-N 0.000 description 1
- CJQNJRMLJAAXOS-UHFFFAOYSA-N 5-prop-1-enylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(C=CC)CC1C=C2 CJQNJRMLJAAXOS-UHFFFAOYSA-N 0.000 description 1
- UGJBFMMPNVKBPX-UHFFFAOYSA-N 5-propan-2-ylidenebicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(=C(C)C)CC1C=C2 UGJBFMMPNVKBPX-UHFFFAOYSA-N 0.000 description 1
- OOVQLEHBRDIXDZ-UHFFFAOYSA-N 7-ethenylbicyclo[4.2.0]octa-1,3,5-triene Chemical class C1=CC=C2C(C=C)CC2=C1 OOVQLEHBRDIXDZ-UHFFFAOYSA-N 0.000 description 1
- 241001556567 Acanthamoeba polyphaga mimivirus Species 0.000 description 1
- 241000234282 Allium Species 0.000 description 1
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Classifications
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- 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
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- 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
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- 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
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
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- 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
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- 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
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
- C08L23/0807—Copolymers of ethene with unsaturated hydrocarbons only containing four or more carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Graft Or Block Polymers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
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| US94967007P | 2007-07-13 | 2007-07-13 |
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| SG183028A1 true SG183028A1 (en) | 2012-08-30 |
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| SG2012052015A SG183028A1 (en) | 2007-07-13 | 2008-07-14 | Ethylene/a-olefin interpolymers containing low crystallinity hard blocks |
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| WO (1) | WO2009012215A1 (cg-RX-API-DMAC7.html) |
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| US8492322B2 (en) * | 2007-07-13 | 2013-07-23 | Dow Global Technologies, Llc | Viscosity index improver for lubricant compositions |
| BRPI0812644B1 (pt) * | 2007-07-13 | 2019-07-09 | Dow Global Technologies Inc. | Interpolímero em bloco de etileno/a-olefina |
| CN101802150A (zh) * | 2007-07-13 | 2010-08-11 | 陶氏环球技术公司 | 润滑剂组合物的粘度指数改性剂 |
| WO2010151433A1 (en) | 2009-06-26 | 2010-12-29 | Dow Global Technologies Inc. | Process selectively polymerizing ethylene and catalyst therefor |
| WO2011016992A2 (en) | 2009-07-29 | 2011-02-10 | Dow Global Technologies Inc. | Polymeric chain transfer/shuttling agents |
| EP3489264B1 (en) | 2009-07-29 | 2021-08-25 | Dow Global Technologies LLC | Chain shuttling agents and their use for the preparation of block copolymers |
| US8324416B2 (en) | 2009-07-29 | 2012-12-04 | Dow Global Technologies, Llc | Multifunctional chain shuttling agents |
| ES2638913T3 (es) | 2009-08-31 | 2017-10-24 | Dow Global Technologies Llc | Catalizador y procedimiento para polimerizar una olefina y poliolefina preparada mediante el mismo |
| US8716400B2 (en) | 2009-10-02 | 2014-05-06 | Dow Global Technologies Llc | Block composites and impact modified compositions |
| JP2013506743A (ja) | 2009-10-02 | 2013-02-28 | ダウ グローバル テクノロジーズ エルエルシー | ソフトコンパウンドにおけるブロックコポリマー |
| CN102770487B (zh) | 2009-10-02 | 2014-10-01 | 陶氏环球技术有限责任公司 | 热塑性硫化材料应用中的嵌段复合材料 |
| WO2011041696A1 (en) | 2009-10-02 | 2011-04-07 | Dow Global Technologies Inc. | Block composites and impact modified compositions |
| US8202954B2 (en) | 2010-02-19 | 2012-06-19 | Dow Global Technologies Llc | Metal-ligand complexes and catalysts |
| WO2011102990A2 (en) | 2010-02-19 | 2011-08-25 | Dow Global Technologies Llc | Process for polymerizing an olefin monomer and catalyst therefor |
| MX375966B (es) | 2010-05-17 | 2025-03-06 | Dow Global Technologies Llc | Proceso para polimerizacion selectiva de etileno y un catalizador del mismo. |
| WO2011163191A1 (en) | 2010-06-21 | 2011-12-29 | Dow Global Technologies Llc | Crystalline block composites as compatibilizers |
| KR101820183B1 (ko) | 2010-06-21 | 2018-01-18 | 다우 글로벌 테크놀로지스 엘엘씨 | 상용화제로서 결정질 블록 복합물 |
| US8785554B2 (en) | 2010-06-21 | 2014-07-22 | Dow Global Technologies Llc | Crystalline block composites as compatibilizers |
| EP2609123B1 (en) | 2010-08-25 | 2017-12-13 | Dow Global Technologies LLC | Process for polymerizing a polymerizable olefin and catalyst therefor |
| MX340414B (es) | 2010-09-30 | 2016-07-06 | Dow Global Tech Llc * | Composición polimérica y capa selladora con la misma. |
| BR112013007274B1 (pt) | 2010-09-30 | 2021-08-10 | Dow Global Technologies Ll | Composição polimérica, película e bolsa de retorta |
| WO2012061706A1 (en) | 2010-11-04 | 2012-05-10 | Dow Global Technologies Llc | Double shuttling of polyolefin polymeryl chains |
| WO2012103080A1 (en) | 2011-01-26 | 2012-08-02 | Dow Global Technologies Llc | Process for making a polyolefin-polysiloxane block copolymer |
| US9296836B2 (en) | 2011-05-12 | 2016-03-29 | Dow Global Technologies Llc | Non-cyclopentadienyl-based chromium catalysts for olefin polymerization |
| ES2667692T3 (es) * | 2011-06-30 | 2018-05-14 | Dow Global Technologies Llc | Películas basadas en poliolefina multicapeadas que tienen una capa que comprende un material compuesto de copolímero en bloque cristalino o una resina de material compuesto de copolímero en bloque |
| EP2727151B1 (en) | 2011-06-30 | 2021-09-01 | Dow Global Technologies LLC | Multilayered polyolefin-based films having integrated backsheet and encapsulation performance comprising a layer comprising crystalline block copolymer composite |
| CN103958548B (zh) | 2011-12-02 | 2016-05-18 | 住友化学株式会社 | 使用多种过渡金属催化剂的烯烃嵌段聚合物的制造方法 |
| SG10201700173TA (en) | 2011-12-14 | 2017-03-30 | Dow Global Technologies Llc | Functionalized block composite and crystalline block composite compositions |
| SG11201402933PA (en) | 2011-12-14 | 2014-07-30 | Dow Global Technologies Llc | Functionalized block composite and crystalline block composite compositions as compatibilizers |
| CN104220551A (zh) | 2012-03-30 | 2014-12-17 | 陶氏环球技术有限责任公司 | 聚烯烃粘合剂组合物 |
| US8691916B2 (en) | 2012-05-07 | 2014-04-08 | Dow Global Technologies Llc | Retortable easy opening seals for film extrusion |
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| EP2895328B1 (en) | 2012-09-14 | 2017-01-04 | Dow Global Technologies LLC | Multilayered polyolefin-based films |
| ES2750647T3 (es) | 2013-10-15 | 2020-03-26 | Dow Global Technologies Llc | Mezclas de poliolefinas compatibilizadas |
| CN105612449B (zh) | 2013-10-18 | 2020-06-23 | 陶氏环球技术有限责任公司 | 光纤缆线组件 |
| WO2015061440A1 (en) | 2013-10-25 | 2015-04-30 | Dow Global Technologies Llc | Polyethylene and polypropylene composition suitable for the use as retortable easy opening seals |
| RU2675843C1 (ru) | 2013-12-18 | 2018-12-25 | ДАУ ГЛОБАЛ ТЕКНОЛОДЖИЗ ЭлЭлСи | Компоненты волоконно-оптического кабеля |
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| KR102603978B1 (ko) | 2015-09-10 | 2023-11-20 | 다우 글로벌 테크놀로지스 엘엘씨 | 상용화제와 함께 폴리옥텐을 포함하는 폴리올레핀 블렌드 |
| WO2017058910A1 (en) | 2015-09-30 | 2017-04-06 | Dow Global Technologies Llc | Multi- or dual-headed compositions useful for chain shuttling and process to prepare the same |
| KR102635693B1 (ko) | 2015-09-30 | 2024-02-14 | 다우 글로벌 테크놀로지스 엘엘씨 | 알데하이드 모이어티에 아미노 및 폴리메릴 기의 첨가를 통한 작용성 폴리머의 제조 방법 |
| WO2017100175A1 (en) | 2015-12-10 | 2017-06-15 | Dow Global Technologies Llc | High modulus olefin compounds for fiber optic cable buffer tubes |
| EP3433315B1 (en) | 2016-03-25 | 2021-02-17 | Dow Global Technologies LLC | Buffer tubes for fiber optic cables |
| WO2017172936A1 (en) | 2016-03-31 | 2017-10-05 | Dow Global Technologies Llc | Polyolefin blends including crystalline block composites for pvc-free wear layers |
| EP3293002A1 (en) | 2016-09-09 | 2018-03-14 | Dow Global Technologies LLC | Multilayer films and laminates and packages formed from same |
| EP3519188B1 (en) | 2016-09-28 | 2024-05-08 | Dow Global Technologies LLC | Multilayer film and pouch with same |
| WO2018064553A1 (en) | 2016-09-30 | 2018-04-05 | Dow Global Technologies Llc | Multi- or dual-headed compositions useful for chain shuttling and process to prepare the same |
| TW201819391A (zh) | 2016-09-30 | 2018-06-01 | 美商陶氏全球科技有限責任公司 | 用於製備適用於鏈梭移之多頭或雙頭組合物之方法 |
| BR112019006150B1 (pt) | 2016-09-30 | 2023-02-28 | Dow Global Technologies Llc | Composição e processo para preparar a composição |
| ES2847374T3 (es) | 2016-10-12 | 2021-08-03 | Dow Global Technologies Llc | Estructuras multicapa, artículos que constituyen las mismas y métodos de fabricación de estructuras multicapa |
| EP3372401B1 (en) | 2017-03-10 | 2020-02-05 | Dow Global Technologies Llc | Multilayer films and methods thereof |
| CN110612315B (zh) | 2017-03-15 | 2022-08-26 | 陶氏环球技术有限责任公司 | 用于形成多嵌段共聚物的催化剂体系 |
| SG11201908306TA (en) | 2017-03-15 | 2019-10-30 | Dow Global Technologies Llc | Catalyst system for multi-block copolymer formation |
| BR112019019076A2 (pt) | 2017-03-15 | 2020-06-30 | Dow Global Technologies Llc | sistema catalisador de formação de copolímeros de múltiplos blocos |
| CN110603274B (zh) | 2017-03-15 | 2022-09-30 | 陶氏环球技术有限责任公司 | 用于形成多嵌段共聚物的催化剂体系 |
| WO2018170138A1 (en) | 2017-03-15 | 2018-09-20 | Dow Global Technologies Llc | Catalyst system for multi-block copolymer formation |
| CA3068528A1 (en) | 2017-06-29 | 2019-01-03 | Dow Global Technologies Llc | Plastic living hinges with block composite polymer |
| EP3655480B1 (en) | 2017-07-18 | 2022-07-27 | Dow Global Technologies LLC | Resins, multilayer films and packages comprising the same |
| EP3431546A1 (en) | 2017-07-18 | 2019-01-23 | Dow Global Technologies Llc | Resins, multilayer films and packages comprising the same |
| EP3732211B1 (en) | 2017-12-29 | 2024-05-22 | Dow Global Technologies Llc | Capped dual-headed organoaluminum compositions |
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| AU2019257331C1 (en) | 2018-04-17 | 2022-05-05 | Henkel Ag & Co. Kgaa | Contact adhesives and uses thereof |
| JP7334195B2 (ja) | 2018-07-17 | 2023-08-28 | ダウ シリコーンズ コーポレーション | ポリシロキサン樹脂－ポリオレフィンコポリマー並びにその調製方法及び使用方法 |
| JP7368465B2 (ja) | 2018-11-06 | 2023-10-24 | ダウ グローバル テクノロジーズ エルエルシー | オレフィンブロックコポリマーおよびそれから作製された物品を用いた付加製造 |
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| ES3040148T3 (en) | 2018-12-28 | 2025-10-28 | Dow Global Technologies Llc | Organometallic chain transfer agents |
| CN113454130B (zh) | 2018-12-28 | 2024-12-13 | 陶氏环球技术有限责任公司 | 遥爪聚烯烃和用于制备遥爪聚烯烃的方法 |
| WO2021041618A1 (en) | 2019-08-29 | 2021-03-04 | Dow Global Technologies Llc | Polymer blends having improved thermal properties |
| US20220306890A1 (en) | 2019-10-11 | 2022-09-29 | Dow Global Technologies Llc | Additive manufacturing using recycled polyolefins with olefin block copolymers and articles made therefrom |
| CN114929661B (zh) | 2019-12-30 | 2024-11-08 | 陶氏环球技术有限责任公司 | 用于制备α-取代的丙烯酸酯的方法 |
| EP4085043B1 (en) | 2019-12-30 | 2025-11-12 | Dow Global Technologies LLC | Process for preparing an alpha-substituted acrylate |
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| WO2021231362A1 (en) | 2020-05-12 | 2021-11-18 | Exxonmobil Chemical Patents Inc. | Thermoplastic elastomer compositions for use in pharmaceutical articles |
| US20230406985A1 (en) | 2020-11-10 | 2023-12-21 | Dow Global Technologies Llc | Preparation of polyolefin-polyacrylate block copolymers additives for increasing surface energy of polyethylene |
| JP2023552056A (ja) | 2020-11-10 | 2023-12-14 | ダウ グローバル テクノロジーズ エルエルシー | ビニル末端ポリオレフィンを介した非極性－極性ブロックコポリマーの調製 |
| EP4259702A1 (en) | 2020-12-14 | 2023-10-18 | Dow Global Technologies LLC | Polyolefin foam beads and process for producing the same |
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| WO2023150921A1 (en) | 2022-02-09 | 2023-08-17 | Dow Global Technologies Llc | A 3d loop article and method for preparing the same |
| KR20250076606A (ko) | 2022-09-30 | 2025-05-29 | 다우 글로벌 테크놀로지스 엘엘씨 | 충격 강도 및 광투과율이 우수한 폴리올레핀 조성물 |
| WO2025019115A1 (en) | 2023-07-20 | 2025-01-23 | Dow Global Technologies Llc | Spunbond nonwoven comprising a mixture of fibers |
| WO2025072678A1 (en) | 2023-09-29 | 2025-04-03 | Dow Global Technologies Llc | Process for preparing an olefin-acrylate block copolymer |
| WO2025096765A1 (en) | 2023-10-31 | 2025-05-08 | Dow Global Technologies Llc | Ethylene-based polymer compositions for tpo applications |
| EP4596231A1 (en) | 2024-01-31 | 2025-08-06 | Dow Global Technologies LLC | Tie layers comprising crystalline block composite components and functionalized polyethylene and multilayer films incorporating same |
| EP4596232A1 (en) | 2024-01-31 | 2025-08-06 | Dow Global Technologies LLC | Tie layers comprising crystalline block composite components and functionalized polyethylene and coated substrates incorporating same |
| WO2025207892A1 (en) | 2024-03-28 | 2025-10-02 | Dow Global Technologies Llc | Olefin-based polymer compositions with good impact performance, stiffness and light transmittance |
Family Cites Families (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4792595A (en) | 1983-06-15 | 1988-12-20 | Exxon Research & Engineering Co. | Narrow MWD alpha-olefin copolymers |
| US4507515A (en) | 1983-12-21 | 1985-03-26 | Exxon Research & Engineering Co. | Lubricating oil compositions containing ethylene-alpha-olefin polymers of controlled sequence distribution and molecular heterogeneity |
| US4927888A (en) | 1986-09-05 | 1990-05-22 | The Dow Chemical Company | Maleic anhydride graft copolymers having low yellowness index and films containing the same |
| US4762890A (en) | 1986-09-05 | 1988-08-09 | The Dow Chemical Company | Method of grafting maleic anhydride to polymers |
| US4950541A (en) | 1984-08-15 | 1990-08-21 | The Dow Chemical Company | Maleic anhydride grafts of olefin polymers |
| US4798081A (en) | 1985-11-27 | 1989-01-17 | The Dow Chemical Company | High temperature continuous viscometry coupled with analytic temperature rising elution fractionation for evaluating crystalline and semi-crystalline polymers |
| US4804794A (en) | 1987-07-13 | 1989-02-14 | Exxon Chemical Patents Inc. | Viscosity modifier polymers |
| US5244590A (en) | 1989-10-12 | 1993-09-14 | Exxon Chemical Patents Inc. | Viscosity index improver |
| US5310490A (en) | 1991-03-13 | 1994-05-10 | Exxon Chemical Products Inc. | Viscosity modifer polymers |
| US5310814A (en) | 1991-03-15 | 1994-05-10 | Exxon Chemical Patents Inc. | Viscosity modifier polybutadiene polymers |
| KR970702308A (ko) | 1994-04-06 | 1997-05-13 | 카텐헤드 벤 씨 | 에틸렌 α-올레핀 블록 공중합체 및 그의 제조 방법(ETHYLENE α-OLEFIN BLOCK COPOLYMERS AND METHODS FOR PRODUCTION THEREOF) |
| BR9507297A (pt) * | 1994-04-06 | 1997-09-30 | Exxon Chemical Patents Inc | Copolimeros de blocos de etileno alfa-olefina e processos para produção dos mesmos |
| DE69702506T2 (de) | 1996-03-27 | 2001-03-08 | The Dow Chemical Co., Midland | Hochlösliches aktivierungsmittel für olefinpolymerisationskatalysator |
| EP0923589B1 (en) | 1996-08-08 | 2004-09-15 | Dow Global Technologies Inc. | 3-heteroatom substituted cyclopentadienyl-containing metal complexes and olefin polymerization process |
| AU749065B2 (en) | 1998-02-20 | 2002-06-20 | Dow Chemical Company, The | Catalyst activators comprising expanded anions |
| JP4558951B2 (ja) | 1999-03-30 | 2010-10-06 | 三井化学株式会社 | 潤滑油用粘度調整剤および潤滑油組成物 |
| US6825295B2 (en) | 1999-12-10 | 2004-11-30 | Dow Global Technologies Inc. | Alkaryl-substituted group 4 metal complexes, catalysts and olefin polymerization process |
| MXPA03004960A (es) | 2000-12-04 | 2004-04-02 | Exxonmobil Chem Patents Inc | Composiciones de copolimero de etileno adecuadas para composiciones mejoradas del indice de viscosidad y lubricantes. |
| US20030004268A1 (en) * | 2001-05-14 | 2003-01-02 | General Electric Company | Polyimide blends, method of making, and articles made therefrom |
| JP4100961B2 (ja) * | 2001-05-31 | 2008-06-11 | 三井化学株式会社 | オレフィンブロック共重合体、潤滑油用粘度指数向上剤および潤滑油組成物 |
| US6960635B2 (en) | 2001-11-06 | 2005-11-01 | Dow Global Technologies Inc. | Isotactic propylene copolymers, their preparation and use |
| US6919467B2 (en) | 2001-12-18 | 2005-07-19 | Univation Technologies, Llc | Imino-amide catalyst compositions for the polymerization of olefins |
| DE60335459D1 (de) | 2002-04-24 | 2011-02-03 | Symyx Solutions Inc | Verbrückte bi-aromatische liganden, komplexe, katalysatoren, verfahren zur polymerisierung und entstehende polymere |
| US7102006B2 (en) | 2002-09-12 | 2006-09-05 | Dow Global Technologies Inc. | Preparation of metal complexes |
| US6953764B2 (en) | 2003-05-02 | 2005-10-11 | Dow Global Technologies Inc. | High activity olefin polymerization catalyst and process |
| US7714071B2 (en) | 2004-03-17 | 2010-05-11 | Dow Global Technologies Inc. | Polymer blends from interpolymers of ethylene/α-olefins and flexible molded articles made therefrom |
| US7355089B2 (en) * | 2004-03-17 | 2008-04-08 | Dow Global Technologies Inc. | Compositions of ethylene/α-olefin multi-block interpolymer for elastic films and laminates |
| US7608668B2 (en) | 2004-03-17 | 2009-10-27 | Dow Global Technologies Inc. | Ethylene/α-olefins block interpolymers |
| MXPA06010485A (es) | 2004-03-17 | 2006-12-19 | Dow Global Technologies Inc | Composicion catalizadora que comprende agente de enlace para la formacion de copolimeros de etileno. |
| AU2005224259B2 (en) | 2004-03-17 | 2010-09-09 | Dow Global Technologies Inc. | Catalyst composition comprising shuttling agent for ethylene multi-block copolymer formation |
| MXPA06010481A (es) | 2004-03-17 | 2006-12-19 | Dow Global Technologies Inc | Composicion catalizadora que comprende agente de enlace para la formacion de copolimeros de multiples bloques de olefina superior. |
| WO2006101932A2 (en) * | 2005-03-17 | 2006-09-28 | Dow Global Technologies Inc. | FILLED POLYMER COMPOSITIONS MADE FROM INTERPOLYMERS OF ETHYLENE/α-OLEFINS AND USES THEREOF |
| BRPI0609819A2 (pt) | 2005-03-17 | 2010-04-27 | Dow Global Technologies Inc | composição lubrificante |
| AU2006227617B2 (en) * | 2005-03-17 | 2011-12-22 | Dow Global Technologies Llc | Ethylene/alpha-olefins block interpolymers |
| AR056281A1 (es) | 2005-03-17 | 2007-10-03 | Dow Global Technologies Inc | Mejorador del indice de viscosidad para composiciones lubricantes |
| BRPI0617001B1 (pt) * | 2005-09-15 | 2018-02-14 | Dow Global Technologies Inc. | Processo para a polimerização de um ou mais monômeros polimerizáveis por adição, copolímero de alto peso molecular e mistura de polímeros |
| BRPI0812644B1 (pt) | 2007-07-13 | 2019-07-09 | Dow Global Technologies Inc. | Interpolímero em bloco de etileno/a-olefina |
| US8492322B2 (en) | 2007-07-13 | 2013-07-23 | Dow Global Technologies, Llc | Viscosity index improver for lubricant compositions |
| CN101802150A (zh) | 2007-07-13 | 2010-08-11 | 陶氏环球技术公司 | 润滑剂组合物的粘度指数改性剂 |
| KR101668120B1 (ko) * | 2008-01-30 | 2016-10-20 | 다우 글로벌 테크놀로지스 엘엘씨 | 에틸렌/α-올레핀 블록 혼성중합체 |
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