JP2000514857A - 弾性重合体およびそれの製造方法 - Google Patents
弾性重合体およびそれの製造方法Info
- Publication number
- JP2000514857A JP2000514857A JP10506243A JP50624398A JP2000514857A JP 2000514857 A JP2000514857 A JP 2000514857A JP 10506243 A JP10506243 A JP 10506243A JP 50624398 A JP50624398 A JP 50624398A JP 2000514857 A JP2000514857 A JP 2000514857A
- Authority
- JP
- Japan
- Prior art keywords
- dimethyl
- silanetitanium
- silane titanium
- methylindenyl
- diisopropoxy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 229920000642 polymer Polymers 0.000 title claims abstract description 82
- 238000004519 manufacturing process Methods 0.000 title claims description 14
- 238000000034 method Methods 0.000 claims abstract description 85
- 239000002904 solvent Substances 0.000 claims abstract description 84
- 238000006243 chemical reaction Methods 0.000 claims abstract description 69
- 239000003054 catalyst Substances 0.000 claims abstract description 62
- 150000001993 dienes Chemical class 0.000 claims abstract description 46
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 45
- 239000005977 Ethylene Substances 0.000 claims abstract description 45
- 239000004711 α-olefin Substances 0.000 claims abstract description 43
- 239000007787 solid Substances 0.000 claims abstract description 33
- 239000000178 monomer Substances 0.000 claims abstract description 32
- 238000011084 recovery Methods 0.000 claims abstract description 30
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 21
- 239000012190 activator Substances 0.000 claims abstract description 12
- 239000000047 product Substances 0.000 claims description 76
- 239000007795 chemical reaction product Substances 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 4
- 238000012986 modification Methods 0.000 claims description 2
- 230000004048 modification Effects 0.000 claims description 2
- 230000000379 polymerizing effect Effects 0.000 abstract description 2
- ZCBSOTLLNBJIEK-UHFFFAOYSA-N silane titanium Chemical compound [SiH4].[Ti] ZCBSOTLLNBJIEK-UHFFFAOYSA-N 0.000 description 760
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 286
- -1 that is Polymers 0.000 description 182
- HBGGBCVEFUPUNY-UHFFFAOYSA-N cyclododecanamine Chemical compound NC1CCCCCCCCCCC1 HBGGBCVEFUPUNY-UHFFFAOYSA-N 0.000 description 140
- 125000001891 dimethoxy group Chemical group [H]C([H])([H])O* 0.000 description 140
- 125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 description 139
- QWUWMCYKGHVNAV-UHFFFAOYSA-N 1,2-dihydrostilbene Chemical group C=1C=CC=CC=1CCC1=CC=CC=C1 QWUWMCYKGHVNAV-UHFFFAOYSA-N 0.000 description 109
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 104
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 103
- JFLKFZNIIQFQBS-FNCQTZNRSA-N trans,trans-1,4-Diphenyl-1,3-butadiene Chemical compound C=1C=CC=CC=1\C=C\C=C\C1=CC=CC=C1 JFLKFZNIIQFQBS-FNCQTZNRSA-N 0.000 description 59
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical compound C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 description 51
- 229910000077 silane Inorganic materials 0.000 description 41
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 40
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 37
- DKNWSYNQZKUICI-UHFFFAOYSA-N amantadine Chemical compound C1C(C2)CC3CC2CC1(N)C3 DKNWSYNQZKUICI-UHFFFAOYSA-N 0.000 description 35
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 35
- 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 27
- 230000003647 oxidation Effects 0.000 description 26
- 238000007254 oxidation reaction Methods 0.000 description 26
- 150000001450 anions Chemical class 0.000 description 23
- 230000008569 process Effects 0.000 description 22
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 21
- 125000001183 hydrocarbyl group Chemical group 0.000 description 21
- 229910052751 metal Inorganic materials 0.000 description 21
- 239000002184 metal Substances 0.000 description 21
- 238000006116 polymerization reaction Methods 0.000 description 17
- 230000004913 activation Effects 0.000 description 16
- 239000003446 ligand Substances 0.000 description 16
- 239000000203 mixture Substances 0.000 description 16
- 230000003213 activating effect Effects 0.000 description 14
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 13
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 description 12
- 230000000737 periodic effect Effects 0.000 description 12
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 11
- 229910052796 boron Inorganic materials 0.000 description 11
- 239000003153 chemical reaction reagent Substances 0.000 description 11
- 150000004696 coordination complex Chemical class 0.000 description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- WVLVQQZPXUGTTK-UHFFFAOYSA-N C1(=CC=CC=C1)C=CC=CC1=CC=CC=C1.[La+2] Chemical compound C1(=CC=CC=C1)C=CC=CC1=CC=CC=C1.[La+2] WVLVQQZPXUGTTK-UHFFFAOYSA-N 0.000 description 10
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 10
- 230000007935 neutral effect Effects 0.000 description 10
- 229910052757 nitrogen Inorganic materials 0.000 description 10
- 239000003115 supporting electrolyte Substances 0.000 description 10
- 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 9
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 9
- 150000001768 cations Chemical class 0.000 description 9
- 238000005868 electrolysis reaction Methods 0.000 description 9
- 229910052739 hydrogen Inorganic materials 0.000 description 9
- 239000001257 hydrogen Substances 0.000 description 9
- 239000000463 material Substances 0.000 description 9
- BNCWJGVCZSBZRK-UHFFFAOYSA-N C=CC=CC.[La+2] Chemical compound C=CC=CC.[La+2] BNCWJGVCZSBZRK-UHFFFAOYSA-N 0.000 description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 8
- 239000003426 co-catalyst Substances 0.000 description 8
- 239000000835 fiber Substances 0.000 description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 8
- 229920001577 copolymer Polymers 0.000 description 7
- 125000004122 cyclic group Chemical group 0.000 description 7
- 229940060942 methylin Drugs 0.000 description 7
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 6
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical group [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 6
- 125000004429 atom Chemical group 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- UORVGPXVDQYIDP-UHFFFAOYSA-N borane Chemical compound B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 description 6
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 description 6
- 150000002500 ions Chemical class 0.000 description 6
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 6
- 125000000538 pentafluorophenyl group Chemical group FC1=C(F)C(F)=C(*)C(F)=C1F 0.000 description 6
- 229910052698 phosphorus Inorganic materials 0.000 description 6
- 239000011574 phosphorus Substances 0.000 description 6
- 229910052719 titanium Inorganic materials 0.000 description 6
- 239000010936 titanium Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical class O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- GQEZCXVZFLOKMC-UHFFFAOYSA-N 1-hexadecene Chemical compound CCCCCCCCCCCCCCC=C GQEZCXVZFLOKMC-UHFFFAOYSA-N 0.000 description 5
- 239000002879 Lewis base Substances 0.000 description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 5
- 150000001336 alkenes Chemical class 0.000 description 5
- 229910052782 aluminium Inorganic materials 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 125000000129 anionic group Chemical group 0.000 description 5
- 125000003118 aryl group Chemical group 0.000 description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 5
- 238000006758 bulk electrolysis reaction Methods 0.000 description 5
- 125000002091 cationic group Chemical group 0.000 description 5
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- IQUIFCKVSZISBH-UHFFFAOYSA-N penta-1,3-diene;titanium(2+) Chemical compound [Ti+2].CC=CC=C IQUIFCKVSZISBH-UHFFFAOYSA-N 0.000 description 5
- 230000009257 reactivity Effects 0.000 description 5
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 5
- 229910052717 sulfur Inorganic materials 0.000 description 5
- 239000011593 sulfur Substances 0.000 description 5
- 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 4
- XWJBRBSPAODJER-UHFFFAOYSA-N 1,7-octadiene Chemical compound C=CCCCCC=C XWJBRBSPAODJER-UHFFFAOYSA-N 0.000 description 4
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 4
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 4
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical compound CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 4
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 4
- HFDVRLIODXPAHB-UHFFFAOYSA-N 1-tetradecene Chemical compound CCCCCCCCCCCCC=C HFDVRLIODXPAHB-UHFFFAOYSA-N 0.000 description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 229910000085 borane Inorganic materials 0.000 description 4
- 239000003085 diluting agent Substances 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- 239000012467 final product Substances 0.000 description 4
- 229910052731 fluorine Inorganic materials 0.000 description 4
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 4
- 229910052737 gold Inorganic materials 0.000 description 4
- 239000010931 gold Substances 0.000 description 4
- 125000005843 halogen group Chemical group 0.000 description 4
- 238000005304 joining Methods 0.000 description 4
- VAMFXQBUQXONLZ-UHFFFAOYSA-N n-alpha-eicosene Natural products CCCCCCCCCCCCCCCCCCC=C VAMFXQBUQXONLZ-UHFFFAOYSA-N 0.000 description 4
- SJYNFBVQFBRSIB-UHFFFAOYSA-N norbornadiene Chemical compound C1=CC2C=CC1C2 SJYNFBVQFBRSIB-UHFFFAOYSA-N 0.000 description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 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
- FDTQPWCIJGYMNG-UHFFFAOYSA-N 4-phenylbuta-1,3-dienylbenzene;titanium(2+) Chemical compound [Ti+2].C=1C=CC=CC=1C=CC=CC1=CC=CC=C1 FDTQPWCIJGYMNG-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 3
- 239000007848 Bronsted acid Substances 0.000 description 3
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 3
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- 239000004793 Polystyrene Substances 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical group [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 3
- BEIOEBMXPVYLRY-UHFFFAOYSA-N [4-[4-bis(2,4-ditert-butylphenoxy)phosphanylphenyl]phenyl]-bis(2,4-ditert-butylphenoxy)phosphane Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(C=1C=CC(=CC=1)C=1C=CC(=CC=1)P(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C BEIOEBMXPVYLRY-UHFFFAOYSA-N 0.000 description 3
- 150000003863 ammonium salts Chemical class 0.000 description 3
- 239000001273 butane Substances 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- 238000005227 gel permeation chromatography Methods 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 229910052735 hafnium Chemical group 0.000 description 3
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical group [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 description 3
- 150000004820 halides Chemical group 0.000 description 3
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000007527 lewis bases Chemical class 0.000 description 3
- 239000012968 metallocene catalyst Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 3
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 3
- 239000007800 oxidant agent Substances 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 229920002223 polystyrene Polymers 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000000376 reactant Substances 0.000 description 3
- SCABQASLNUQUKD-UHFFFAOYSA-N silylium Chemical class [SiH3+] SCABQASLNUQUKD-UHFFFAOYSA-N 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- 229910052726 zirconium Inorganic materials 0.000 description 3
- QXALIERKYGCHHA-UHFFFAOYSA-N (2,3,4,5,6-pentafluorophenyl)borane Chemical compound BC1=C(F)C(F)=C(F)C(F)=C1F QXALIERKYGCHHA-UHFFFAOYSA-N 0.000 description 2
- PRBHEGAFLDMLAL-GQCTYLIASA-N (4e)-hexa-1,4-diene Chemical compound C\C=C\CC=C PRBHEGAFLDMLAL-GQCTYLIASA-N 0.000 description 2
- RJUCIROUEDJQIB-GQCTYLIASA-N (6e)-octa-1,6-diene Chemical compound C\C=C\CCCC=C RJUCIROUEDJQIB-GQCTYLIASA-N 0.000 description 2
- PRBHEGAFLDMLAL-UHFFFAOYSA-N 1,5-Hexadiene Natural products CC=CCC=C PRBHEGAFLDMLAL-UHFFFAOYSA-N 0.000 description 2
- 229940106006 1-eicosene Drugs 0.000 description 2
- FIKTURVKRGQNQD-UHFFFAOYSA-N 1-eicosene Natural products CCCCCCCCCCCCCCCCCC=CC(O)=O FIKTURVKRGQNQD-UHFFFAOYSA-N 0.000 description 2
- ICKWICRCANNIBI-UHFFFAOYSA-N 2,4-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C(C(C)(C)C)=C1 ICKWICRCANNIBI-UHFFFAOYSA-N 0.000 description 2
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 2
- INYHZQLKOKTDAI-UHFFFAOYSA-N 5-ethenylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(C=C)CC1C=C2 INYHZQLKOKTDAI-UHFFFAOYSA-N 0.000 description 2
- WTQBISBWKRKLIJ-UHFFFAOYSA-N 5-methylidenebicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(=C)CC1C=C2 WTQBISBWKRKLIJ-UHFFFAOYSA-N 0.000 description 2
- UCKITPBQPGXDHV-UHFFFAOYSA-N 7-methylocta-1,6-diene Chemical compound CC(C)=CCCCC=C UCKITPBQPGXDHV-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- JMJOHZJRPWRGTF-UHFFFAOYSA-N CN(C)C1=CC=CC=C1.CN(C)C1=CC=CC=C1.CN(C)C1=CC=CC=C1.OB(O)O Chemical compound CN(C)C1=CC=CC=C1.CN(C)C1=CC=CC=C1.CN(C)C1=CC=CC=C1.OB(O)O JMJOHZJRPWRGTF-UHFFFAOYSA-N 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- KVOZXXSUSRZIKD-UHFFFAOYSA-N Prop-2-enylcyclohexane Chemical compound C=CCC1CCCCC1 KVOZXXSUSRZIKD-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- UORVGPXVDQYIDP-BJUDXGSMSA-N borane Chemical class [10BH3] UORVGPXVDQYIDP-BJUDXGSMSA-N 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 2
- 235000013539 calcium stearate Nutrition 0.000 description 2
- 239000008116 calcium stearate Substances 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 150000001983 dialkylethers Chemical class 0.000 description 2
- 229940069096 dodecene Drugs 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000806 elastomer Substances 0.000 description 2
- HEAMQYHBJQWOSS-UHFFFAOYSA-N ethene;oct-1-ene Chemical compound C=C.CCCCCCC=C HEAMQYHBJQWOSS-UHFFFAOYSA-N 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 125000001153 fluoro group Chemical group F* 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical group 0.000 description 2
- OTTZHAVKAVGASB-UHFFFAOYSA-N hept-2-ene Chemical compound CCCCC=CC OTTZHAVKAVGASB-UHFFFAOYSA-N 0.000 description 2
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical compound C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 2
- 150000004678 hydrides Chemical class 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- AWJFCAXSGQLCKK-UHFFFAOYSA-N icosa-1,19-diene Chemical compound C=CCCCCCCCCCCCCCCCCC=C AWJFCAXSGQLCKK-UHFFFAOYSA-N 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 150000002738 metalloids Chemical group 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methylcycloheptane Chemical compound CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 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
- 239000008188 pellet Substances 0.000 description 2
- QYZLKGVUSQXAMU-UHFFFAOYSA-N penta-1,4-diene Chemical compound C=CCC=C QYZLKGVUSQXAMU-UHFFFAOYSA-N 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229910052697 platinum Inorganic materials 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 239000002685 polymerization catalyst Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 229920001897 terpolymer Polymers 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 229920002397 thermoplastic olefin Polymers 0.000 description 2
- YWWDBCBWQNCYNR-UHFFFAOYSA-N trimethylphosphine Chemical compound CP(C)C YWWDBCBWQNCYNR-UHFFFAOYSA-N 0.000 description 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 2
- AEIBHAUJIARVOJ-UHFFFAOYSA-N (2-dihydroxyphosphanylphenyl)phosphonous acid Chemical group OP(O)C1=CC=CC=C1P(O)O AEIBHAUJIARVOJ-UHFFFAOYSA-N 0.000 description 1
- LOQCUTBYNXEZNX-UHFFFAOYSA-N (2-fluorophenyl)borane Chemical compound BC1=CC=CC=C1F LOQCUTBYNXEZNX-UHFFFAOYSA-N 0.000 description 1
- BOGRNZQRTNVZCZ-AATRIKPKSA-N (3e)-3-methylpenta-1,3-diene Chemical compound C\C=C(/C)C=C BOGRNZQRTNVZCZ-AATRIKPKSA-N 0.000 description 1
- ZTJHDEXGCKAXRZ-FNORWQNLSA-N (3e)-octa-1,3,7-triene Chemical compound C=CCC\C=C\C=C ZTJHDEXGCKAXRZ-FNORWQNLSA-N 0.000 description 1
- LRIUTQPZISVIHK-FNORWQNLSA-N (3e)-tetradeca-1,3-diene Chemical compound CCCCCCCCCC\C=C\C=C LRIUTQPZISVIHK-FNORWQNLSA-N 0.000 description 1
- TVEFFNLPYIEDLS-VQHVLOKHSA-N (4e)-deca-1,4,9-triene Chemical compound C=CCCC\C=C\CC=C TVEFFNLPYIEDLS-VQHVLOKHSA-N 0.000 description 1
- GOYDNIKZWGIXJT-UHFFFAOYSA-N 1,2-difluorobenzene Chemical compound FC1=CC=CC=C1F GOYDNIKZWGIXJT-UHFFFAOYSA-N 0.000 description 1
- BOGRNZQRTNVZCZ-UHFFFAOYSA-N 1,2-dimethyl-butadiene Natural products CC=C(C)C=C BOGRNZQRTNVZCZ-UHFFFAOYSA-N 0.000 description 1
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 1
- JVTMVUFBBYUSKS-UHFFFAOYSA-N 1,4-bis(prop-2-enyl)benzene Chemical compound C=CCC1=CC=C(CC=C)C=C1 JVTMVUFBBYUSKS-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
- MLRVZFYXUZQSRU-UHFFFAOYSA-N 1-chlorohexane Chemical compound CCCCCCCl MLRVZFYXUZQSRU-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
- BDAJBOIAMYRWFR-UHFFFAOYSA-N 1-methyl-2-(2-methylphenyl)sulfanylbenzene Chemical compound CC1=CC=CC=C1SC1=CC=CC=C1C BDAJBOIAMYRWFR-UHFFFAOYSA-N 0.000 description 1
- UZGKAASZIMOAMU-UHFFFAOYSA-N 124177-85-1 Chemical class NP(=O)=O UZGKAASZIMOAMU-UHFFFAOYSA-N 0.000 description 1
- 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 1
- CMSUNVGIWAFNBG-UHFFFAOYSA-N 2,4-dimethylpenta-1,3-diene Chemical compound CC(C)=CC(C)=C CMSUNVGIWAFNBG-UHFFFAOYSA-N 0.000 description 1
- LAGGTOBQMQHXON-UHFFFAOYSA-N 2,6-octadiene Chemical compound CC=CCCC=CC LAGGTOBQMQHXON-UHFFFAOYSA-N 0.000 description 1
- IOHAVGDJBFVWGE-UHFFFAOYSA-N 2-ethylidene-3-propan-2-ylidenebicyclo[2.2.1]hept-5-ene Chemical compound C1C2C=CC1C(=CC)C2=C(C)C IOHAVGDJBFVWGE-UHFFFAOYSA-N 0.000 description 1
- SLQMKNPIYMOEGB-UHFFFAOYSA-N 2-methylhexa-1,5-diene Chemical compound CC(=C)CCC=C SLQMKNPIYMOEGB-UHFFFAOYSA-N 0.000 description 1
- AQZWEFBJYQSQEH-UHFFFAOYSA-N 2-methyloxaluminane Chemical compound C[Al]1CCCCO1 AQZWEFBJYQSQEH-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- VOXXWSYKYCBWHO-UHFFFAOYSA-N 3-phenyllactic acid Chemical compound OC(=O)C(O)CC1=CC=CC=C1 VOXXWSYKYCBWHO-UHFFFAOYSA-N 0.000 description 1
- VXMJXJAHNOJRAA-UHFFFAOYSA-N 4,7,7-trimethylbicyclo[2.2.1]hepta-2,5-diene Chemical compound C1=CC2(C)C=CC1C2(C)C VXMJXJAHNOJRAA-UHFFFAOYSA-N 0.000 description 1
- BBDKZWKEPDTENS-UHFFFAOYSA-N 4-Vinylcyclohexene Chemical compound C=CC1CCC=CC1 BBDKZWKEPDTENS-UHFFFAOYSA-N 0.000 description 1
- 239000004915 4-vinylcyclohex-1-ene Substances 0.000 description 1
- VVVBPWHIKKPKBD-UHFFFAOYSA-N B([O-])([O-])[O-].FC1=C(C(=CC(=C1F)F)F)[N+](C)(C)C.FC1=C(C(=CC(=C1F)F)F)[N+](C)(C)C.FC1=C(C(=CC(=C1F)F)F)[N+](C)(C)C Chemical compound B([O-])([O-])[O-].FC1=C(C(=CC(=C1F)F)F)[N+](C)(C)C.FC1=C(C(=CC(=C1F)F)F)[N+](C)(C)C.FC1=C(C(=CC(=C1F)F)F)[N+](C)(C)C VVVBPWHIKKPKBD-UHFFFAOYSA-N 0.000 description 1
- JGIVXYNQCKAONW-UHFFFAOYSA-N B([O-])([O-])[O-].FC1=C(C(=CC(=C1F)F)F)[N+](CCC)(CCC)CCC.FC1=C(C(=CC(=C1F)F)F)[N+](CCC)(CCC)CCC.FC1=C(C(=CC(=C1F)F)F)[N+](CCC)(CCC)CCC Chemical compound B([O-])([O-])[O-].FC1=C(C(=CC(=C1F)F)F)[N+](CCC)(CCC)CCC.FC1=C(C(=CC(=C1F)F)F)[N+](CCC)(CCC)CCC.FC1=C(C(=CC(=C1F)F)F)[N+](CCC)(CCC)CCC JGIVXYNQCKAONW-UHFFFAOYSA-N 0.000 description 1
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical compound N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 description 1
- BITRMKOZMVUJPI-UHFFFAOYSA-N CC(C)(C)[Si](C)(C)C(C(F)=C(C(OB(O)O)=C1F)F)=C1F.CN(C)C1=CC=CC=C1.CN(C)C1=CC=CC=C1 Chemical compound CC(C)(C)[Si](C)(C)C(C(F)=C(C(OB(O)O)=C1F)F)=C1F.CN(C)C1=CC=CC=C1.CN(C)C1=CC=CC=C1 BITRMKOZMVUJPI-UHFFFAOYSA-N 0.000 description 1
- XWYBUIBMXHCTNE-UHFFFAOYSA-N CC(C)[Si](C(C)C)(C(C)C)C(C(F)=C(C(OB(O)O)=C1F)F)=C1F.CN(C)C1=CC=CC=C1.CN(C)C1=CC=CC=C1 Chemical compound CC(C)[Si](C(C)C)(C(C)C)C(C(F)=C(C(OB(O)O)=C1F)F)=C1F.CN(C)C1=CC=CC=C1.CN(C)C1=CC=CC=C1 XWYBUIBMXHCTNE-UHFFFAOYSA-N 0.000 description 1
- JEOAJQXYAWKASO-UHFFFAOYSA-N CC(C=C1C)=CC(C)=C1N(C)C.CC(C=C1C)=CC(C)=C1N(C)C.OB(O)OC(C(F)=C(C(F)=C1F)F)=C1F Chemical compound CC(C=C1C)=CC(C)=C1N(C)C.CC(C=C1C)=CC(C)=C1N(C)C.OB(O)OC(C(F)=C(C(F)=C1F)F)=C1F JEOAJQXYAWKASO-UHFFFAOYSA-N 0.000 description 1
- SJUWBAMFAOHZKC-UHFFFAOYSA-N CC(C=C1C)=CC(C)=C1N(C)C.CC(C=C1C)=CC(C)=C1N(C)C.OB(O)OC(C(F)=CC(F)=C1F)=C1F Chemical compound CC(C=C1C)=CC(C)=C1N(C)C.CC(C=C1C)=CC(C)=C1N(C)C.OB(O)OC(C(F)=CC(F)=C1F)=C1F SJUWBAMFAOHZKC-UHFFFAOYSA-N 0.000 description 1
- SWYHSFREXSDNHJ-UHFFFAOYSA-N CC(C=CC=C1)=C1OC1=C(C)C=CC=C1.CC(C=CC=C1)=C1OC1=C(C)C=CC=C1.OB(O)OC(C(F)=C(C(F)=C1F)F)=C1F Chemical compound CC(C=CC=C1)=C1OC1=C(C)C=CC=C1.CC(C=CC=C1)=C1OC1=C(C)C=CC=C1.OB(O)OC(C(F)=C(C(F)=C1F)F)=C1F SWYHSFREXSDNHJ-UHFFFAOYSA-N 0.000 description 1
- SEMSDXRNUGFYPW-UHFFFAOYSA-N CC(C=CC=C1C)=C1SC1=C(C)C=CC=C1C.CC(C=CC=C1C)=C1SC1=C(C)C=CC=C1C.CC(C=CC=C1C)=C1SC1=C(C)C=CC=C1C.OB(O)O Chemical compound CC(C=CC=C1C)=C1SC1=C(C)C=CC=C1C.CC(C=CC=C1C)=C1SC1=C(C)C=CC=C1C.CC(C=CC=C1C)=C1SC1=C(C)C=CC=C1C.OB(O)O SEMSDXRNUGFYPW-UHFFFAOYSA-N 0.000 description 1
- GWTZZXHALJDQPV-UHFFFAOYSA-N CCC(C)N(C(C)CC)C(C)CC.CCC(C)N(C(C)CC)C(C)CC.CCC(C)N(C(C)CC)C(C)CC.OB(O)O Chemical compound CCC(C)N(C(C)CC)C(C)CC.CCC(C)N(C(C)CC)C(C)CC.CCC(C)N(C(C)CC)C(C)CC.OB(O)O GWTZZXHALJDQPV-UHFFFAOYSA-N 0.000 description 1
- ATUMANLNMNACOK-UHFFFAOYSA-N CCCCN(CCCC)C(CCC(C(C(F)=C(C(F)=C1F)F)=C1F)(C(C(F)=C(C(F)=C1F)F)=C1F)C(C(F)=C(C(F)=C1F)F)=C1F)C(C(F)=C(C(F)=C1F)F)=C1F.CCCCN(CCCC)C(CCC(C(C(F)=C(C(F)=C1F)F)=C1F)(C(C(F)=C(C(F)=C1F)F)=C1F)C(C(F)=C(C(F)=C1F)F)=C1F)C(C(F)=C(C(F)=C1F)F)=C1F.CCCCN(CCCC)C(CCC(C(C(F)=C(C(F)=C1F)F)=C1F)(C(C(F)=C(C(F)=C1F)F)=C1F)C(C(F)=C(C(F)=C1F)F)=C1F)C(C(F)=C(C(F)=C1F)F)=C1F.OB(O)O Chemical compound CCCCN(CCCC)C(CCC(C(C(F)=C(C(F)=C1F)F)=C1F)(C(C(F)=C(C(F)=C1F)F)=C1F)C(C(F)=C(C(F)=C1F)F)=C1F)C(C(F)=C(C(F)=C1F)F)=C1F.CCCCN(CCCC)C(CCC(C(C(F)=C(C(F)=C1F)F)=C1F)(C(C(F)=C(C(F)=C1F)F)=C1F)C(C(F)=C(C(F)=C1F)F)=C1F)C(C(F)=C(C(F)=C1F)F)=C1F.CCCCN(CCCC)C(CCC(C(C(F)=C(C(F)=C1F)F)=C1F)(C(C(F)=C(C(F)=C1F)F)=C1F)C(C(F)=C(C(F)=C1F)F)=C1F)C(C(F)=C(C(F)=C1F)F)=C1F.OB(O)O ATUMANLNMNACOK-UHFFFAOYSA-N 0.000 description 1
- PZJSWVRAJDUZOX-UHFFFAOYSA-N CCCN(CCC)CCC.CCCN(CCC)CCC.CCCN(CCC)CCC.OB(O)O Chemical compound CCCN(CCC)CCC.CCCN(CCC)CCC.CCCN(CCC)CCC.OB(O)O PZJSWVRAJDUZOX-UHFFFAOYSA-N 0.000 description 1
- YOIDKMZYSPERQX-UHFFFAOYSA-N CCN(CC)C(C(C(C(F)=CC(F)=C1F)=C1F)(C(C(F)=CC(F)=C1F)=C1F)C(C(F)=CC(F)=C1F)=C1F)C(C(F)=CC(F)=C1F)=C1F.CCN(CC)C(C(C(C(F)=CC(F)=C1F)=C1F)(C(C(F)=CC(F)=C1F)=C1F)C(C(F)=CC(F)=C1F)=C1F)C(C(F)=CC(F)=C1F)=C1F.CCN(CC)C(C(C(C(F)=CC(F)=C1F)=C1F)(C(C(F)=CC(F)=C1F)=C1F)C(C(F)=CC(F)=C1F)=C1F)C(C(F)=CC(F)=C1F)=C1F.OB(O)O Chemical compound CCN(CC)C(C(C(C(F)=CC(F)=C1F)=C1F)(C(C(F)=CC(F)=C1F)=C1F)C(C(F)=CC(F)=C1F)=C1F)C(C(F)=CC(F)=C1F)=C1F.CCN(CC)C(C(C(C(F)=CC(F)=C1F)=C1F)(C(C(F)=CC(F)=C1F)=C1F)C(C(F)=CC(F)=C1F)=C1F)C(C(F)=CC(F)=C1F)=C1F.CCN(CC)C(C(C(C(F)=CC(F)=C1F)=C1F)(C(C(F)=CC(F)=C1F)=C1F)C(C(F)=CC(F)=C1F)=C1F)C(C(F)=CC(F)=C1F)=C1F.OB(O)O YOIDKMZYSPERQX-UHFFFAOYSA-N 0.000 description 1
- WREUEIJSHIDLBG-UHFFFAOYSA-N CCN(CC)C1=CC=CC=C1.CCN(CC)C1=CC=CC=C1.CCN(CC)C1=CC=CC=C1.OB(O)O Chemical compound CCN(CC)C1=CC=CC=C1.CCN(CC)C1=CC=CC=C1.CCN(CC)C1=CC=CC=C1.OB(O)O WREUEIJSHIDLBG-UHFFFAOYSA-N 0.000 description 1
- ZNVIHZVLJWKKAL-UHFFFAOYSA-N CCN(CC)C1=CC=CC=C1.CCN(CC)C1=CC=CC=C1.OB(O)OC(C(F)=C(C(F)=C1F)F)=C1F Chemical compound CCN(CC)C1=CC=CC=C1.CCN(CC)C1=CC=CC=C1.OB(O)OC(C(F)=C(C(F)=C1F)F)=C1F ZNVIHZVLJWKKAL-UHFFFAOYSA-N 0.000 description 1
- MELQNULAXMEKNN-UHFFFAOYSA-N CCN(CC)CC.CCN(CC)CC.CCN(CC)CC.OB(O)O Chemical compound CCN(CC)CC.CCN(CC)CC.CCN(CC)CC.OB(O)O MELQNULAXMEKNN-UHFFFAOYSA-N 0.000 description 1
- PUWYWTXQZCYDSC-UHFFFAOYSA-N CN(C)C1=CC=CC=C1.CN(C)C1=CC=CC=C1.OB(O)OC(C(F)=C(C(F)=C1F)F)=C1F Chemical compound CN(C)C1=CC=CC=C1.CN(C)C1=CC=CC=C1.OB(O)OC(C(F)=C(C(F)=C1F)F)=C1F PUWYWTXQZCYDSC-UHFFFAOYSA-N 0.000 description 1
- LRQFXPSVOKKTFC-UHFFFAOYSA-N CN(C)C1=CC=CC=C1.CN(C)C1=CC=CC=C1.OB(O)OC(C(F)=CC(F)=C1F)=C1F Chemical compound CN(C)C1=CC=CC=C1.CN(C)C1=CC=CC=C1.OB(O)OC(C(F)=CC(F)=C1F)=C1F LRQFXPSVOKKTFC-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 244000304337 Cuminum cyminum Species 0.000 description 1
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 1
- 229920002943 EPDM rubber Polymers 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 241001441571 Hiodontidae Species 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- 229910000799 K alloy Inorganic materials 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 101000867030 Myxine glutinosa Homeobox protein engrailed-like B Proteins 0.000 description 1
- 229910000528 Na alloy Inorganic materials 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
- LXZKCKFSRRAAKG-UHFFFAOYSA-N OB(O)O.C(C=C1)=CC=C1SC1=CC=CC=C1.C(C=C1)=CC=C1SC1=CC=CC=C1.C(C=C1)=CC=C1SC1=CC=CC=C1 Chemical compound OB(O)O.C(C=C1)=CC=C1SC1=CC=CC=C1.C(C=C1)=CC=C1SC1=CC=CC=C1.C(C=C1)=CC=C1SC1=CC=CC=C1 LXZKCKFSRRAAKG-UHFFFAOYSA-N 0.000 description 1
- MKJDNIZTFUOTNB-UHFFFAOYSA-N OB(O)O.C(CC1)CCC1NC1CCCCC1.C(CC1)CCC1NC1CCCCC1.C(CC1)CCC1NC1CCCCC1 Chemical compound OB(O)O.C(CC1)CCC1NC1CCCCC1.C(CC1)CCC1NC1CCCCC1.C(CC1)CCC1NC1CCCCC1 MKJDNIZTFUOTNB-UHFFFAOYSA-N 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 229910000978 Pb alloy Inorganic materials 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 241001061127 Thione Species 0.000 description 1
- 229910052770 Uranium Inorganic materials 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910000573 alkali metal alloy Inorganic materials 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 229910000941 alkaline earth metal alloy Inorganic materials 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 1
- 150000001502 aryl halides Chemical class 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 238000000071 blow moulding Methods 0.000 description 1
- 238000005885 boration reaction Methods 0.000 description 1
- XZKRXPZXQLARHH-UHFFFAOYSA-N buta-1,3-dienylbenzene Chemical compound C=CC=CC1=CC=CC=C1 XZKRXPZXQLARHH-UHFFFAOYSA-N 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 125000005626 carbonium group Chemical group 0.000 description 1
- 238000003763 carbonization Methods 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 150000004292 cyclic ethers Chemical class 0.000 description 1
- UVJHQYIOXKWHFD-UHFFFAOYSA-N cyclohexa-1,4-diene Chemical compound C1C=CCC=C1 UVJHQYIOXKWHFD-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 230000009849 deactivation Effects 0.000 description 1
- NLDGJRWPPOSWLC-UHFFFAOYSA-N deca-1,9-diene Chemical compound C=CCCCCCCC=C NLDGJRWPPOSWLC-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 238000004807 desolvation Methods 0.000 description 1
- 125000002897 diene group Chemical group 0.000 description 1
- CXVAUNIKYTWEFC-UHFFFAOYSA-N dimethoxyborinic acid Chemical compound COB(O)OC CXVAUNIKYTWEFC-UHFFFAOYSA-N 0.000 description 1
- JLTDJTHDQAWBAV-UHFFFAOYSA-O dimethyl(phenyl)azanium Chemical compound C[NH+](C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-O 0.000 description 1
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 238000006056 electrooxidation reaction Methods 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- LDLDYFCCDKENPD-UHFFFAOYSA-N ethenylcyclohexane Chemical compound C=CC1CCCCC1 LDLDYFCCDKENPD-UHFFFAOYSA-N 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 125000004407 fluoroaryl group Chemical group 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 150000004795 grignard reagents Chemical class 0.000 description 1
- GEAWFZNTIFJMHR-UHFFFAOYSA-N hepta-1,6-diene Chemical compound C=CCCCC=C GEAWFZNTIFJMHR-UHFFFAOYSA-N 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- QPRFPZGRQQKMEX-UHFFFAOYSA-N lanthanum(2+) Chemical compound [La+2] QPRFPZGRQQKMEX-UHFFFAOYSA-N 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 239000012092 media component Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229910052752 metalloid Inorganic materials 0.000 description 1
- CPOFMOWDMVWCLF-UHFFFAOYSA-N methyl(oxo)alumane Chemical class C[Al]=O CPOFMOWDMVWCLF-UHFFFAOYSA-N 0.000 description 1
- JUHDUIDUEUEQND-UHFFFAOYSA-N methylium Chemical group [CH3+] JUHDUIDUEUEQND-UHFFFAOYSA-N 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 125000004043 oxo group Chemical group O=* 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
- 150000004714 phosphonium salts Chemical class 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 238000007142 ring opening reaction Methods 0.000 description 1
- 238000001175 rotational moulding Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 150000004819 silanols Chemical class 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- JLKIGFTWXXRPMT-UHFFFAOYSA-N sulphamethoxazole Chemical compound O1C(C)=CC(NS(=O)(=O)C=2C=CC(N)=CC=2)=N1 JLKIGFTWXXRPMT-UHFFFAOYSA-N 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229920006029 tetra-polymer Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000004634 thermosetting polymer Substances 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 150000005671 trienes Chemical class 0.000 description 1
- RXJKFRMDXUJTEX-UHFFFAOYSA-N triethylphosphine Chemical compound CCP(CC)CC RXJKFRMDXUJTEX-UHFFFAOYSA-N 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- ANEFWEBMQHRDLH-UHFFFAOYSA-N tris(2,3,4,5,6-pentafluorophenyl) borate Chemical compound FC1=C(F)C(F)=C(F)C(F)=C1OB(OC=1C(=C(F)C(F)=C(F)C=1F)F)OC1=C(F)C(F)=C(F)C(F)=C1F ANEFWEBMQHRDLH-UHFFFAOYSA-N 0.000 description 1
- 238000007666 vacuum forming Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 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
- C08F297/00—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
- C08F297/06—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type
- C08F297/08—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type polymerising mono-olefins
-
- 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
- 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
- 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
- C08F210/18—Copolymers of ethene with alpha-alkenes, e.g. EP rubbers with non-conjugated dienes, e.g. EPT rubbers
-
- 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 more than three carbon atoms
- C08L23/0815—Copolymers of ethene with aliphatic 1-olefins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F110/00—Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F110/02—Ethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- 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
- C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
- C08F4/65904—Component covered by group C08F4/64 containing a transition metal-carbon bond in combination with another component of C08F4/64
-
- 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
- C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
- C08F4/65908—Component covered by group C08F4/64 containing a transition metal-carbon bond in combination with an ionising compound other than alumoxane, e.g. (C6F5)4B-X+
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
- C08F4/65912—Component covered by group C08F4/64 containing a transition metal-carbon bond in combination with an organoaluminium compound
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/659—Component covered by group C08F4/64 containing a transition metal-carbon bond
- C08F4/6592—Component covered by group C08F4/64 containing a transition metal-carbon bond containing at least one cyclopentadienyl ring, condensed or not, e.g. an indenyl or a fluorenyl ring
-
- 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
- C08L23/16—Elastomeric ethene-propene or ethene-propene-diene copolymers, e.g. EPR and EPDM rubbers
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polymerisation Methods In General (AREA)
- Graft Or Block Polymers (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Description
Claims (1)
- 【特許請求の範囲】 1. エチレン/α−オレフィン単量体から作られた重合体およびエチレン/ α−オレフィン/ジエン単量体から作られた重合体を製造する方法であって、下 記の段階: A. 第一反応槽内で(1)エチレン、(2)少なくとも1種のC3−C20脂 肪族α−オレフィン、(3)任意に少なくとも1種のC4−C20ジエン、(4) (a)メタロセン錯体と(b)少なくとも1種の活性化剤を含む触媒、および( 5)溶媒を接触させて、この第一反応槽を、第一生成物が該第一反応槽内の反応 マスの重量を基準にして1から15重量パーセントの固体濃度で生じるように操 作し、 B. 第二反応槽内で(1)エチレン、(2)少なくとも1種のC3−C20脂 肪族α−オレフィン、(3)任意に少なくとも1種のC4−C20ジエン、(4) (a)メタロセン錯体と(b)少なくとも1種の活性化剤を含む触媒、(5)溶 媒、および(6)第一反応槽から来る生成物流れを接触させて、この第二反応槽 を、第二生成物が該第二反応槽内の反応マスの重量を基準にして2から30重量 パーセントの固体濃度で生じるように操作し、 C. 該第二反応槽から生成物流れを取り出し、 D. 第一段階の無水溶媒回収操作において、該生成物流れの固体濃度が少な くとも100パーセント高くなるように該第二反応槽の生成物流れから溶媒を除 去し、そして E.第二段階の無水溶媒回収操作において、該生成物流れの固体濃度が65重 量パーセントを越えるように該第一段階の溶媒回収操作の生成物から追加的に溶 媒を除去する、 段階を用いることを特徴とする方法。 2. エチレン/α−オレフィン単量体から作られた重合体およびエチレン/ α−オレフィン/ジエン単量体から作られた重合体を製造する方法であって、下 記の段階: A. 第一反応槽内で(1)エチレン、(2)少なくとも1種のC3−C20脂 肪族α−オレフィン、(3)任意に少なくとも1種のC4−C20ジエン、(4) (a)メタロセン錯体と(b)少なくとも1種の活性化剤を含む触媒、および( 5)溶媒を接触させて、この第一反応槽を、第一生成物が該第一反応槽内の反応 マスの重量を基準にして1から30重量パーセントの固体濃度で生じるように操 作し、 B. 第二反応槽内で(1)エチレン、(2)少なくとも1種のC3−C20脂 肪族α−オレフィン、(3)任意に少なくとも1種のC4−C20ジエン、(4) (a)メタロセン錯体と(b)少なくとも1種の活性化剤を含む触媒、および( 5)溶媒を接触させて、この第二反応槽を、第二生成物が該第二反応槽内の反応 マスの重量を基準にして1から30重量パーセントの固体濃度で生じるように操 作し、 C. 該第一反応槽および第二反応槽の各々から生成物流れを回収した後、こ れらの個々の生成物流れをブレンドして一緒になった生成物流れを生じさせ、 D. 第一段階の無水溶媒回収操作において、その一緒になった生成物流れの 固体濃度が少なくとも100パーセント高くなるようにその一緒になった生成物 流れから溶媒を除去し、そして E.第二段階の無水溶媒回収操作において、その一緒になった生成物流れの固 体濃度が65重量パーセントを越えるようにその一緒になった 生成物流れから追加的に溶媒を除去する、 段階を用いることを特徴とする方法。 3. 該第一段階の溶媒回収操作後のある地点で該第二反応槽の生成物の流動 学的修飾を行う追加的段階を用いることを更に特徴とする請求の範囲第1または 2項いずれか記載の方法。 4. 請求の範囲第1−3項いずれかの方法で作られた重合体。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/679,538 US6545088B1 (en) | 1991-12-30 | 1996-07-12 | Metallocene-catalyzed process for the manufacture of EP and EPDM polymers |
US08/679,538 | 1996-07-12 | ||
PCT/US1997/012294 WO1998002471A1 (en) | 1996-07-12 | 1997-07-09 | Elastomers and process for their manufacture |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2000514857A true JP2000514857A (ja) | 2000-11-07 |
Family
ID=24727319
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10506243A Pending JP2000514857A (ja) | 1996-07-12 | 1997-07-09 | 弾性重合体およびそれの製造方法 |
Country Status (19)
Country | Link |
---|---|
US (1) | US6545088B1 (ja) |
EP (1) | EP0910593B1 (ja) |
JP (1) | JP2000514857A (ja) |
KR (1) | KR100496101B1 (ja) |
CN (1) | CN1098289C (ja) |
AT (1) | ATE200680T1 (ja) |
AU (1) | AU718342B2 (ja) |
BR (1) | BR9710347A (ja) |
CA (1) | CA2256668C (ja) |
CZ (1) | CZ9499A3 (ja) |
DE (1) | DE69704617T2 (ja) |
ES (1) | ES2156001T3 (ja) |
HU (1) | HUP9904354A3 (ja) |
NO (1) | NO990095L (ja) |
NZ (1) | NZ332880A (ja) |
PL (1) | PL331038A1 (ja) |
TR (1) | TR199900050T2 (ja) |
TW (1) | TW341576B (ja) |
WO (1) | WO1998002471A1 (ja) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002528610A (ja) * | 1998-11-02 | 2002-09-03 | デュポン ダウ エラストマーズ エルエルシー | 剪断減粘性エチレン/α−オレフィンインターポリマーおよびそれらの製造法 |
JP2003507541A (ja) * | 1999-08-19 | 2003-02-25 | デユポン・ダウ・エラストマーズ・エル・エル・シー | 幅広い分子量分布を示すポリマーブレンド物を単一の反応槽内で製造する方法 |
JP2008516068A (ja) * | 2004-10-13 | 2008-05-15 | エクソンモービル・ケミカル・パテンツ・インク | エラストマー性反応ブレンド組成物 |
JP2008525546A (ja) * | 2004-12-23 | 2008-07-17 | ボレアリス テクノロジー オイ | コポリマー |
JP2011529522A (ja) * | 2008-07-29 | 2011-12-08 | アルケマ フランス | 再生可能な材料からのグラフト化ポリエチレンの製造、得られるポリエチレン、およびその使用 |
JP2012533653A (ja) * | 2009-07-15 | 2012-12-27 | ダウ グローバル テクノロジーズ エルエルシー | ポリマー組成物、その製造方法及びそれから製造される物品 |
JP2015521692A (ja) * | 2012-08-31 | 2015-07-30 | エクソンモービル ケミカル パテンツ インコーポレイテッド | ポリマーを形成するためのプラントおよび方法 |
Families Citing this family (173)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20010041560A (ko) | 1998-03-04 | 2001-05-25 | 엑손 케미칼 패턴츠 인코포레이티드 | 이피디엠형 중합에서 디엔 전환을 증가시키는 방법 |
US6319998B1 (en) | 1998-03-04 | 2001-11-20 | Exxon Mobil Chemical Patents Inc. | Method for making polymer blends by using series reactors |
AU2796899A (en) | 1998-03-04 | 1999-09-20 | Exxon Chemical Patents Inc. | Product and method for making polyolefin polymer dispersions |
JP4566305B2 (ja) * | 1999-08-31 | 2010-10-20 | 日本ポリプロ株式会社 | メタロセン化合物由来成分を含有する溶剤の精製方法 |
EP2267042B1 (en) | 2000-01-26 | 2015-06-10 | Mitsui Chemicals, Inc. | Olefin diblock copolymer of very low polydispersity and process for preparing the same |
ATE337341T1 (de) | 2000-10-25 | 2006-09-15 | Exxonmobil Chem Patents Inc | Verfahren und vorrichtung zur kontinuierlichen lösungspolymerisation |
WO2002046251A2 (en) * | 2000-12-04 | 2002-06-13 | Exxonmobil Chemical Patents Inc. | Ethylene copolymer compositions suitable for viscosity index improvers and lubricant compositions |
JP2005502731A (ja) * | 2000-12-20 | 2005-01-27 | エクソンモービル・ケミカル・パテンツ・インク | 分岐したポリマー組成物を製造するためのオレフィン重合法 |
US7022766B2 (en) | 2001-05-31 | 2006-04-04 | Mitsui Chemicals, Inc. | Olefin block copolymer, viscosity index improver for lubricating oils and lubricating oil composition |
SG120869A1 (en) * | 2001-05-31 | 2006-04-26 | Mitsui Chemicals Inc | Olefin block copolymer, viscosity index improver for lubricating oils and lubricating oil composition |
ATE407972T1 (de) | 2001-12-12 | 2008-09-15 | Exxonmobil Chem Patents Inc | Für elastomere membranen geeignete zusammensetzungen |
AU2003216210A1 (en) | 2002-02-08 | 2003-09-02 | Exxonmobil Chemical Patents Inc. | Multimodal ethylene, alpha-olefin and diene polymers, processes for making and devices comprising such compositions |
DE60327855D1 (de) | 2002-06-19 | 2009-07-16 | Exxonmobil Chem Patents Inc | Verfahren zur polymerisation von ethylen, höheren alpha-olefin-comonomeren und dienen, insbesondere vinyl norbornen und nach diesem verfahren hergestellte polymere |
WO2004046214A2 (en) | 2002-10-15 | 2004-06-03 | Exxonmobil Chemical Patents Inc. | Multiple catalyst system for olefin polymerization and polymers produced therefrom |
JP4708188B2 (ja) * | 2003-01-23 | 2011-06-22 | 三井化学株式会社 | エチレン・α−オレフィン・非共役ポリエン共重合体の製造方法およびエチレン・α−オレフィン・非共役ポリエン共重合体 |
MXPA05013347A (es) * | 2003-06-10 | 2006-04-05 | Dow Global Technologies Inc | Capas de pelicula hechas a partir de mezclas de polimeros de etileno. |
CN1852959B (zh) | 2003-08-19 | 2010-06-16 | 陶氏环球技术公司 | 适用于热熔粘合剂的共聚体及其制备方法 |
US7084319B2 (en) | 2003-12-05 | 2006-08-01 | Exxonmobil Chemical Patents Inc. | Catalyst fluidization in oxygenate to olefin reaction systems |
AU2005224258B2 (en) | 2004-03-17 | 2010-09-02 | Dow Global Technologies Inc. | Catalyst composition comprising shuttling agent for ethylene copolymer formation |
ES2397701T3 (es) | 2004-03-17 | 2013-03-08 | Dow Global Technologies Llc | Composición de catalizador que comprende un agente de transporte para la formación de un copolímero de multi-bloques de olefina superior |
TW200604224A (en) | 2004-03-17 | 2006-02-01 | Dow Global Technologies Inc | Catalyst composition comprising shuttling agent for ethylene copolymer formation |
GB0420396D0 (en) | 2004-09-14 | 2004-10-13 | Bp Chem Int Ltd | Polyolefins |
KR100586922B1 (ko) | 2004-11-18 | 2006-06-08 | 금호폴리켐 주식회사 | 고수율의 이피(디)엠의 제조방법 및 수율의 제어방법,이피(디)엠의 회수방법 |
AU2005319179B2 (en) * | 2004-12-21 | 2011-10-13 | Dow Global Technologies Llc | Polypropylene-based adhesive compositions |
WO2006083515A1 (en) * | 2005-01-31 | 2006-08-10 | Exxonmobil Chemical Patents Inc. | Polymer blends and pellets and methods of producing same |
CN101142246B (zh) | 2005-03-17 | 2011-05-25 | 陶氏环球技术公司 | 用于形成有规立构/无规立构多嵌段共聚物的包含梭移剂的催化剂组合物 |
ZA200707877B (en) | 2005-03-17 | 2008-12-31 | Dow Global Technologies Inc | Polymer blends from interpolymers of ethyleno/alpha-olefins and flexible molded articles made therefrorr |
US9410009B2 (en) | 2005-03-17 | 2016-08-09 | Dow Global Technologies Llc | Catalyst composition comprising shuttling agent for tactic/ atactic multi-block copolymer formation |
AU2006227976A1 (en) | 2005-03-17 | 2006-09-28 | Dow Global Technologies Inc. | Catalyst composition comprising shuttling agent for regio-irregular multi-block copolymer formation |
US7585917B2 (en) | 2005-06-13 | 2009-09-08 | Exxonmobil Chemical Patents Inc. | Thermoplastic blend compositions |
AR058449A1 (es) | 2005-09-15 | 2008-02-06 | Dow Global Technologies Inc | Copolimeros de bloque de olefina cataliticos via un agente de transferencia polimerizable |
BRPI0617041B1 (pt) * | 2005-09-15 | 2018-01-30 | Dow Global Technologies Inc. | PROCESSO PARA PREPARAR UM POLÍMERO DIFUNCIONAL EM a, ?" |
EP1999168B1 (en) * | 2006-03-30 | 2012-01-25 | Total Petrochemicals Research Feluy | Process for the preparation of ethylene polymers using a number of reactors arranged in series |
CN101395250B (zh) | 2006-03-31 | 2013-06-05 | 埃克森美孚化学专利公司 | 气-固反应器中的产物回收 |
US7744746B2 (en) | 2006-03-31 | 2010-06-29 | Exxonmobil Research And Engineering Company | FCC catalyst stripper configuration |
CN109320664A (zh) | 2006-06-15 | 2019-02-12 | 陶氏环球技术有限责任公司 | 官能化烯烃共聚体、组合物和由其制成的制品及其制法 |
US8785531B2 (en) * | 2006-07-06 | 2014-07-22 | Dow Global Technologies Llc | Dispersions of olefin block copolymers |
TR201814683T4 (tr) | 2006-09-11 | 2018-11-21 | Dow Global Technologies Llc | Reçine kaplı kum için kullanılan poliolefin dispersiyon teknolojisi. |
US8476326B2 (en) * | 2006-09-22 | 2013-07-02 | Dow Global Technologies Llc | Fibrillated polyolefin foam |
BRPI0806751B1 (pt) * | 2007-01-17 | 2018-08-14 | Agrofresh Inc. | Liberação de agentes de bloqueio e/ou promoção de etileno |
RU2010105230A (ru) | 2007-07-16 | 2011-08-27 | Дау Глобал Текнолоджиз Инк. (Us) | Функционализованные полимеры, изделия, полученные из них, и способы их получения |
US8431096B2 (en) | 2007-08-27 | 2013-04-30 | Nova Chemicals (International) S.A | Process for high temperature solution polymerization |
CA2598960C (en) | 2007-08-27 | 2015-04-07 | Nova Chemicals Corporation | High temperature process for solution polymerization |
CA2598957C (en) | 2007-08-27 | 2014-07-15 | Nova Chemicals Corporation | Process for high temperature solution polymerization |
JP2010540799A (ja) * | 2007-09-24 | 2010-12-24 | ダウ グローバル テクノロジーズ インコーポレイティド | 緩衝層を有する人工芝 |
US8318257B2 (en) | 2007-09-28 | 2012-11-27 | Dow Global Technologies Llc | Dispersions of higher crystallinity olefins |
EP2300652B1 (en) * | 2007-10-25 | 2017-08-30 | Dow Global Technologies LLC | Polyolefin dispersion technology used for porous substrates |
US7910679B2 (en) * | 2007-12-20 | 2011-03-22 | Exxonmobil Research And Engineering Company | Bulk homogeneous polymerization process for ethylene propylene copolymers |
WO2009086251A1 (en) | 2007-12-28 | 2009-07-09 | Dow Global Technologies Inc. | Pe-based crosslinked elastomeric foam with high filler loadings for making shockpads and articles used in footwear and flooring applications |
DE102008039218A1 (de) | 2008-08-22 | 2010-02-25 | Woco Industrietechnik Gmbh | Vulkanisierbare Kautschukmischungen sowie Elastomerformteile, erhältlich aus diesen Kautschukmischungen |
US20110172368A1 (en) * | 2008-09-23 | 2011-07-14 | Stolz-Dunn Sandra K | Radically Functionalized Olefin-Based Polymer with Reduced Molecular Weight Change and Method |
US8969481B2 (en) | 2008-12-18 | 2015-03-03 | Exxonmobil Chemical Patent Inc. | Peroxide cured TPV |
KR101707696B1 (ko) | 2009-03-31 | 2017-02-16 | 다우 글로벌 테크놀로지스 엘엘씨 | 불균질 에틸렌/알파-올레핀 혼성중합체로부터 제조된 필름 |
EP2438093B1 (en) | 2009-06-05 | 2013-07-24 | Dow Global Technologies LLC | Process to make long chain branched (lcb), block, or interconnected copolymers of ethylene |
US8722817B2 (en) * | 2009-06-05 | 2014-05-13 | Dow Global Technologies Llc | Process to make long chain branched (LCB), block, or interconnected copolymers of ethylene |
US8173232B2 (en) | 2009-07-01 | 2012-05-08 | Dow Global Technologies Llc | Stretch hood films |
US20120095158A1 (en) | 2009-07-01 | 2012-04-19 | Dow Global Technologies Llc | Ethylenic polymer and its use |
WO2011109563A2 (en) | 2010-03-02 | 2011-09-09 | Dow Global Technologies Llc | Ethylene-based polymer compositions |
US8629214B2 (en) | 2009-07-01 | 2014-01-14 | Dow Global Technologies Llc. | Ethylene-based polymer compositions for use as a blend component in shrinkage film applications |
US8389086B2 (en) | 2009-07-01 | 2013-03-05 | Dow Global Technologies Llc | Composition for stretch hood, method of producing the same, and articles made therefrom |
US20110003940A1 (en) * | 2009-07-01 | 2011-01-06 | Dow Global Technologies Inc. | Ethylene-based polymer compositions for use as a blend component in shrinkage film applications |
EP2448979B1 (en) | 2009-07-01 | 2013-05-01 | Dow Global Technologies LLC | Ethylenic polymer and its use |
KR101262305B1 (ko) | 2009-07-01 | 2013-05-08 | 주식회사 엘지화학 | 전이금속 촉매를 이용한 탄성 중합체의 제조방법 |
ES2651292T3 (es) | 2009-07-29 | 2018-01-25 | Dow Global Technologies Llc | Agentes de transferencia de cadena de doble o múltiple cabeza y su uso para la preparación de copolímeros de bloque |
WO2011032176A1 (en) | 2009-09-14 | 2011-03-17 | Dow Global Technologies Inc. | Polymers comprising units derived from ethylene and polyalkene |
JP5764561B2 (ja) | 2009-09-14 | 2015-08-19 | ダウ グローバル テクノロジーズ エルエルシー | エチレンおよびシロキサン由来の単位を含むポリマー |
WO2011032174A1 (en) | 2009-09-14 | 2011-03-17 | Dow Global Technologies Inc. | Polymers comprising units derived from ethylene and poly(alkoxide) |
US9546446B2 (en) | 2009-10-23 | 2017-01-17 | Toyo Boseki Kabushiki Kaisha | Highly functional polyethylene fibers, woven or knit fabric, and cut-resistant glove |
CN101734996B (zh) * | 2009-12-29 | 2012-12-19 | 岳阳昌德化工实业有限公司 | 一种对含4-乙烯基环己烯的废液回收和利用方法 |
US20110172354A1 (en) * | 2010-01-04 | 2011-07-14 | Dow Global Technologies Inc. | Ethylene-based polymer compositions for use in fiber applications |
US8653196B2 (en) | 2010-01-11 | 2014-02-18 | Dow Global Technologies, Llc | Method for preparing polyethylene with high melt strength |
WO2011087731A1 (en) | 2010-01-14 | 2011-07-21 | Exxonmobil Chemical Patents Inc. | Processes and apparatus for continuous solution polymerization |
RU2012134037A (ru) | 2010-01-14 | 2014-02-20 | Лист Холдинг АГ | Вакуумное устройство для удаления летучих веществ |
US8562915B2 (en) | 2010-01-14 | 2013-10-22 | Exxonmobil Chemical Patents Inc. | Processes and apparatus for polymer finishing and packaging |
WO2011087729A2 (en) | 2010-01-14 | 2011-07-21 | Exxonmobil Chemical Patents Inc. | Processes and apparatus for polymer finishing and packaging |
CN102762604A (zh) | 2010-01-14 | 2012-10-31 | 埃克森美孚化学专利公司 | 连续溶液聚合的方法和设备 |
BR112012030649A2 (pt) | 2010-06-04 | 2016-08-16 | Dow Global Technologies Llc | módulo de dispositivo eletrônico compreendendo película de copolímero de poliolefina homogêneo e polímero de enxerto realçador de propriedade adesiva |
BR112012030650A2 (pt) | 2010-06-04 | 2016-08-16 | Dow Global Technologies Llc | módulo de dispositivo eletrônico compreendendo película de copolímero de poliolefina homogêneo e silano enxertado |
CN103168072B (zh) | 2010-06-14 | 2015-12-16 | 陶氏环球技术有限责任公司 | 用作收缩膜应用中共混物组分的基于乙烯的聚合物组合物 |
EP2585292A1 (en) | 2010-06-24 | 2013-05-01 | Dow Global Technologies LLC | Electronic device module comprising heterogeneous polyolefin copolymer and optionally silane |
WO2012024005A2 (en) | 2010-07-09 | 2012-02-23 | Luna Innovations Incorporated | Coating systems capable of forming ambiently cured highly durable hydrophobic coatings on substrates |
US8907034B2 (en) | 2010-09-30 | 2014-12-09 | Dow Global Technologies Llc | Comb architecture olefin block copolymers |
JP5980219B2 (ja) | 2010-10-29 | 2016-08-31 | ダウ グローバル テクノロジーズ エルエルシー | エチレン系ポリマーおよびその方法 |
US20120116034A1 (en) * | 2010-11-08 | 2012-05-10 | Dow Global Technologies, Inc. | Solution polymerization process and procatalyst carrier systems useful therein |
US8877880B2 (en) | 2010-11-17 | 2014-11-04 | Exxonmobil Chemical Patents Inc. | Method for controlling polyolefin properties |
EP2813545A1 (en) | 2010-12-03 | 2014-12-17 | Dow Global Technologies LLC | Processes to prepare ethylene-based polymer compositions |
CA2724943A1 (en) | 2010-12-10 | 2012-06-10 | Nova Chemicals Corporation | Catalyst activation in a dual reactor process |
ES2605991T3 (es) | 2010-12-17 | 2017-03-17 | Dow Global Technologies Llc | Polímeros basados en etileno y procedimientos para su fabricación |
BR112013016788B1 (pt) | 2010-12-30 | 2021-02-02 | Dow Global Technologies Llc | composição granulada e composição reticulada |
ES2549143T3 (es) | 2011-06-30 | 2015-10-23 | Dow Global Technologies Llc | Películas basadas en poliolefina multicapeadas que tienen una capa que comprende un compuesto de copolímero en bloque cristalino o una resina de compuesto de copolímero en bloque |
US9428595B2 (en) | 2011-07-05 | 2016-08-30 | Dow Global Technologies Llc | Ethylene-based polymers and processes to make the same |
CN103890237A (zh) * | 2011-09-14 | 2014-06-25 | 马特里亚公司 | 含有用第8族烯烃复分解催化剂聚合的树脂组合物的改进电解池盖 |
JP6215209B2 (ja) | 2011-09-30 | 2017-10-18 | ダウ グローバル テクノロジーズ エルエルシー | 剥離制御された積層接着フィルム |
JP6189325B2 (ja) | 2011-12-20 | 2017-08-30 | ダウ グローバル テクノロジーズ エルエルシー | エチレン/アルファオレフィン/非共役ポリエン共重合体およびその形成方法 |
KR101989335B1 (ko) | 2011-12-22 | 2019-06-17 | 다우 글로벌 테크놀로지스 엘엘씨 | 개선된 용융 강도를 가진 에틸렌-기재 중합체 및 그의 제조 방법 |
US8552117B1 (en) | 2012-06-13 | 2013-10-08 | Teknor Apex Company | Sealing elements and sealing element compositions |
US10370524B2 (en) | 2012-06-29 | 2019-08-06 | Dow Global Technologies Llc | Ethylene/alpha-olefin/nonconjugated polyene based compositions for thermoplastic vulcanizates |
US9255168B2 (en) * | 2012-08-16 | 2016-02-09 | Exxonmobil Chemical Patents Inc. | Highly branched compositions and processes for the production thereof |
CN104822713B (zh) | 2012-09-28 | 2018-05-18 | 陶氏环球技术有限公司 | 乙烯基聚合物和其制造方法 |
US8871887B2 (en) | 2012-09-28 | 2014-10-28 | Dow Global Technologies Llc | Ethylene-based polymers and processes to make the same |
KR101391692B1 (ko) | 2012-11-14 | 2014-05-07 | 주식회사 엘지화학 | 3원계 탄성 공중합체 및 이의 제조 방법 |
BR112015010919B1 (pt) | 2012-11-30 | 2021-08-17 | Dow Global Technologies Llc | Composição, composição reticulada e artigo |
SG11201504000YA (en) | 2012-11-30 | 2015-06-29 | Dow Global Technologies Llc | Ethylene/alpha-olefin/nonconjugated polyene based compositions and foams formed from the same |
ES2719257T3 (es) | 2012-12-28 | 2019-07-09 | Dow Global Technologies Llc | Polímeros a base de etileno y procedimientos para preparar los mismos |
KR20140144076A (ko) | 2013-06-10 | 2014-12-18 | 주식회사 엘지화학 | 3원계 탄성 공중합체의 제조 방법 |
KR101585206B1 (ko) | 2013-07-22 | 2016-01-13 | 주식회사 엘지화학 | 디엔을 포함하는 3원계 탄성 공중합체 및 이의 제조 방법 |
US9650460B2 (en) | 2013-06-28 | 2017-05-16 | Lg Chem, Ltd. | Elastic diene terpolymer and preparation method thereof |
US9493593B2 (en) | 2013-06-28 | 2016-11-15 | Lg Chem, Ltd. | Elastic diene terpolymer and preparation method thereof |
WO2014209082A1 (ko) | 2013-06-28 | 2014-12-31 | 주식회사 엘지화학 | 디엔을 포함하는 3원계 탄성 공중합체 및 이의 제조 방법 |
KR101585204B1 (ko) | 2013-06-28 | 2016-01-13 | 주식회사 엘지화학 | 디엔을 포함하는 3원계 탄성 공중합체 및 이의 제조 방법 |
SG11201605159UA (en) | 2013-12-26 | 2016-07-28 | Dow Global Technologies Llc | Processes to improve reactor stability for the preparation of ethylene-based polymers using asymmetrical polyenes |
EP3626752B1 (en) | 2013-12-26 | 2021-04-21 | Dow Global Technologies LLC | Ethylene-based polymers formed using asymmetrical polyenes |
US9718906B2 (en) | 2013-12-26 | 2017-08-01 | Dow Global Technologies Llc | Processes to form ethylene-based polymers using asymmetrical polyenes |
CN108794675B (zh) | 2014-03-21 | 2020-12-29 | 埃克森美孚化学专利公司 | 乙烯丙烯共聚物的制备方法 |
KR101655392B1 (ko) | 2014-04-21 | 2016-09-07 | 주식회사 엘지화학 | 디엔을 포함하는 3원계 탄성 공중합체 및 이의 제조 방법 |
KR101660480B1 (ko) | 2014-04-25 | 2016-09-27 | 주식회사 엘지화학 | 디엔을 포함하는 3원계 탄성 공중합체 및 이의 제조 방법 |
US20170200842A1 (en) | 2014-06-24 | 2017-07-13 | Dow Global Technologies Llc | Photovoltaic Modules Comprising Organoclay |
EP3161059B1 (en) | 2014-06-24 | 2019-07-24 | Dow Global Technologies LLC | Polyolefin photovoltaic backsheet comprising a stabilized polypropylene layer |
US20170152377A1 (en) | 2014-06-26 | 2017-06-01 | Dow Global Technologies Llc | Breathable films and articles incorporating same |
EP3161023A1 (en) | 2014-06-27 | 2017-05-03 | Dow Global Technologies LLC | Ethylene-based polymers comprising units derived from carbon monoxide and a rheology modifying agent |
KR20170027738A (ko) | 2014-06-30 | 2017-03-10 | 다우 글로벌 테크놀로지스 엘엘씨 | 줄무늬 다층 필름 |
EP3227370B1 (en) | 2014-12-01 | 2019-11-20 | Dow Global Technologies LLC | Polymer compositions, shrink films, and methods of making thereof |
US10160817B2 (en) | 2014-12-23 | 2018-12-25 | Dow Global Technologies Llc | Ethylene based interpolymers and composition comprising the same |
WO2016109264A1 (en) | 2014-12-29 | 2016-07-07 | Dow Global Technologies Llc | Process to form ethylene/alpha-olefin interpolymers |
WO2016109265A1 (en) | 2014-12-29 | 2016-07-07 | Dow Global Technologies Llc | Process to form oil containing ethylene-based polymers |
US10273318B2 (en) | 2014-12-30 | 2019-04-30 | Dow Global Technologies Llc | Process to control output and quality of ethylene-based polymer formed by high pressure free radical polymerization |
WO2016160231A1 (en) | 2015-03-31 | 2016-10-06 | Dow Global Technologies Llc | Processes for the production of high molecular weight ethylene/alpha-olefin/non-conjugated interpolymers with low levels of long chain branching |
WO2016176821A1 (en) | 2015-05-05 | 2016-11-10 | Dow Global Technologies Llc | Functionalized, halogenated olefin-based adhesive, articles containing and process for using thereof |
KR102617008B1 (ko) | 2015-06-17 | 2023-12-26 | 다우 글로벌 테크놀로지스 엘엘씨 | 관형 반응기에서 제조되고 그리고 선택적으로 분기제로 변형된 높은 용융 강도의 에틸렌계 폴리머를 사용하여 가교결합된 케이블 절연체를 제조하는 방법 |
FR3037586A1 (fr) | 2015-06-17 | 2016-12-23 | Michelin & Cie | Procede de polymerisation continu d'elastomere dienique |
CN107735414A (zh) | 2015-06-22 | 2018-02-23 | 陶氏环球技术有限责任公司 | 使用碳‑碳自由基引发剂制备基于乙烯的聚合物的方法 |
ES2799524T3 (es) | 2015-06-24 | 2020-12-18 | Dow Global Technologies Llc | Procedimientos para preparar polímeros a base de etileno con resistencia en estado fundido mejorada |
US10400046B2 (en) | 2015-06-25 | 2019-09-03 | Joseph J. Matsko | Portable powered paint system |
WO2017040088A1 (en) | 2015-09-02 | 2017-03-09 | Dow Global Technologies Llc | Flexible crosslinked cable insulation and methods for making flexible crosslinked cable insulation |
EP3345193B1 (en) | 2015-09-02 | 2021-04-21 | Dow Global Technologies LLC | Flexible crosslinked cable insulation and methods for making flexible crosslinked cable insulation |
US10800865B2 (en) | 2015-09-14 | 2020-10-13 | Exxonmobil Chemical Patents Inc. | Process for making branched EPDM and the EPDM therefrom |
WO2017074707A1 (en) | 2015-10-29 | 2017-05-04 | Dow Global Technologies Llc | Crosslinkable polymeric compositions for flexible crosslinked cable insulation and methods for making flexible crosslinked cable insulation |
EP3168238A1 (en) | 2015-11-10 | 2017-05-17 | Dow Global Technologies LLC | Ethylene-based polymers formed by high pressure free radical polymerizations |
EP3168237A1 (en) | 2015-11-10 | 2017-05-17 | Dow Global Technologies LLC | High pressure, free radical polymerizations to produce ethylene-based polymers |
EP3168239A1 (en) | 2015-11-10 | 2017-05-17 | Dow Global Technologies LLC | High pressure free radical polymerizations |
CN108431060B (zh) | 2015-12-29 | 2021-10-26 | 陶氏环球技术有限责任公司 | 高度接枝的基于乙烯的聚合物、高度接枝的基于乙烯的聚合物组合物和其形成方法 |
CN108602997B (zh) | 2016-02-23 | 2021-10-15 | 陶氏环球技术有限责任公司 | 基于乙烯的聚合物和其制备方法 |
ES2926229T3 (es) | 2016-04-29 | 2022-10-24 | Dow Global Technologies Llc | Composiciones que comprenden copolímeros de etileno-monóxido de carbono |
WO2017206009A1 (en) | 2016-05-30 | 2017-12-07 | Dow Global Technologies Llc | Ethylene/alpha-olefin/diene interpolymers compositions |
WO2017206008A1 (en) | 2016-05-30 | 2017-12-07 | Dow Global Technologies Llc | Ethylene/alpha-olefin/diene interpolymer |
CN107474194B (zh) * | 2016-06-08 | 2022-03-18 | 中国石油化工股份有限公司 | 一种高分子聚合物材料的制造方法 |
EP3478762A1 (en) | 2016-06-30 | 2019-05-08 | Dow Global Technologies, LLC | Ethylene/alpha-olefin/polyene based compositions |
WO2018005922A1 (en) | 2016-06-30 | 2018-01-04 | Dow Global Technologies Llc | Ethylene/alpha-olefin/polyene interpolymers and compositions containing the same |
US11161969B2 (en) | 2016-12-16 | 2021-11-02 | Dow Global Technologies Llc | Ethylene/alpha-olefin interpolymer compositions |
US11098183B2 (en) | 2017-02-28 | 2021-08-24 | Dow Global Technologies Llc | Ethylene-based polymers with good processability for use in multilayer films |
CN110709432B (zh) | 2017-06-02 | 2022-09-23 | 陶氏环球技术有限责任公司 | 基于乙烯的聚合物及其制备方法 |
CN111148641B (zh) | 2017-08-24 | 2023-03-31 | 陶氏环球技术有限责任公司 | 乙烯/C5-C10α-烯烃/多烯互聚物 |
CN111278871B (zh) | 2017-10-31 | 2023-09-19 | 陶氏环球技术有限责任公司 | 乙烯/co共聚物和其制备方法 |
EP3480220A1 (en) * | 2017-11-06 | 2019-05-08 | Borealis AG | Combined sequential parallel reactor configuration |
KR101918484B1 (ko) | 2017-11-15 | 2019-01-31 | 금호폴리켐 주식회사 | 탄성 공중합체 제조용 촉매 조성물 및 이를 이용한 에틸렌 및 알파-올레핀 또는 에틸렌, 알파-올레핀 및 비공액 디엔을 포함하는 탄성 공중합체의 제조 방법 |
WO2019156794A1 (en) | 2018-02-09 | 2019-08-15 | Exxonmobil Chemical Patents Inc. | ETHYLENE-α-OLEFIN-DIENE ELASTOMERS AND METHODS OF MAKING THEM |
US11753521B2 (en) | 2018-02-14 | 2023-09-12 | Dow Global Technologies Llc | Ethylene/alpha-olefin interpolymer compositions with improved continuous high temperature resistance |
KR102530938B1 (ko) | 2018-02-14 | 2023-05-11 | 다우 글로벌 테크놀로지스 엘엘씨 | 장기간 열 시효 성능이 개선된 에틸렌/알파-올레핀 혼성중합체 조성물 |
KR102520418B1 (ko) | 2018-02-14 | 2023-04-11 | 다우 글로벌 테크놀로지스 엘엘씨 | 지속적 고온 내열성이 개선된 에틸렌/알파-올레핀 혼성중합체 조성물 |
US11873377B2 (en) | 2018-06-15 | 2024-01-16 | Dow Global Technologies Llc | Blown films comprising bimodal ethylene-based polymers having high molecular weight high density fractions |
CN112399976A (zh) | 2018-06-15 | 2021-02-23 | 陶氏环球技术有限责任公司 | 用于生产具有高分子量高密度级分的基于乙烯的双峰聚合物的方法 |
CN112368327B (zh) | 2018-06-15 | 2023-10-10 | 陶氏环球技术有限责任公司 | 包括具有高分子量高密度级分的基于乙烯的双峰聚合物的流延膜 |
CA3103013A1 (en) | 2018-06-15 | 2019-12-19 | Dow Global Technologies Llc | Bimodal ethylene-based polymers having high molecular weight high density fractions |
BR112020026221A2 (pt) | 2018-06-28 | 2021-04-06 | Dow Global Technologies Llc | Polímero à base de etileno, e, processo |
SG11202107057WA (en) | 2018-12-28 | 2021-07-29 | Dow Global Technologies Llc | Curable compositions comprising unsaturated polyolefins |
WO2020139993A1 (en) | 2018-12-28 | 2020-07-02 | Dow Global Technologies Llc | Curable compositions comprising unsaturated polyolefins |
EP3902852A1 (en) | 2018-12-28 | 2021-11-03 | Dow Global Technologies LLC | Telechelic polyolefins and processes for preparing the same |
BR112021012786A2 (pt) | 2018-12-28 | 2021-09-14 | Dow Global Technologies Llc | Formulação curável |
WO2020243426A1 (en) | 2019-05-31 | 2020-12-03 | Dow Global Technologies Llc | Low density polyethylene with improved processability |
BR112022005433A2 (pt) | 2019-09-24 | 2022-06-21 | Dow Global Technologies Llc | Composição, composição reticulada, e, artigo |
JP2022549317A (ja) | 2019-09-24 | 2022-11-24 | ダウ グローバル テクノロジーズ エルエルシー | 押出形材のためのポリマー組成物 |
US20230151195A1 (en) | 2020-04-06 | 2023-05-18 | Dow Global Technologies Llc | Enhanced melt strength low-density polyethylene for use in films or blends |
MX2023004316A (es) | 2020-10-14 | 2023-05-04 | Dow Global Technologies Llc | Composiciones de polietileno aptas para su uso en peliculas estirables fundidas. |
Family Cites Families (84)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3485706A (en) | 1968-01-18 | 1969-12-23 | Du Pont | Textile-like patterned nonwoven fabrics and their production |
US4200722A (en) | 1971-09-24 | 1980-04-29 | Stamicarbon, B.V. | Rubber-like copolymers of ethylene, at least one other α-alkene and one or more polyenes possessing increased building tack |
US4184027A (en) | 1971-10-26 | 1980-01-15 | Monsanto Company | Recycle control system for continuous polymerization |
US4102761A (en) | 1974-01-03 | 1978-07-25 | The Firestone Tire & Rubber Company | Radiation cure of synthetic rubbers |
JPS5111882A (en) | 1974-07-20 | 1976-01-30 | Sumitomo Chemical Co | Mihannotanryotaio jokyosuruhoho |
FR2297713A1 (fr) | 1975-01-17 | 1976-08-13 | Telecommunications Sa | Procede d'introduction |
FR2322883A1 (fr) | 1975-09-02 | 1977-04-01 | Michelin & Cie | Elastomeres du type e p t, et articles comportant de tels elastomeres |
JPS52141888A (en) | 1976-05-21 | 1977-11-26 | Nippon I P Rubber Kk | Ethyleneepropylene copolymers rubber |
US4075287A (en) | 1976-10-27 | 1978-02-21 | Phillips Petroleum Company | Separation process |
DE2735355A1 (de) | 1977-08-05 | 1979-02-15 | Basf Ag | Verfahren zum herstellen von homo- und copolymerisaten des aethylens |
US4182810A (en) | 1978-04-21 | 1980-01-08 | Phillips Petroleum Company | Prevention of fouling in polymerization reactors |
JPS5948046B2 (ja) | 1978-08-17 | 1984-11-24 | 三井化学株式会社 | エチレン共重合ゴム |
US4340563A (en) | 1980-05-05 | 1982-07-20 | Kimberly-Clark Corporation | Method for forming nonwoven webs |
US4413110A (en) | 1981-04-30 | 1983-11-01 | Allied Corporation | High tenacity, high modulus polyethylene and polypropylene fibers and intermediates therefore |
JPS587402A (ja) | 1981-07-07 | 1983-01-17 | Mitsui Petrochem Ind Ltd | 重合方法 |
US4792595A (en) | 1983-06-15 | 1988-12-20 | Exxon Research & Engineering Co. | Narrow MWD alpha-olefin copolymers |
US4663220A (en) | 1985-07-30 | 1987-05-05 | Kimberly-Clark Corporation | Polyolefin-containing extrudable compositions and methods for their formation into elastomeric products including microfibers |
US4722971A (en) | 1985-08-02 | 1988-02-02 | Exxon Chemical Patents Inc. | Easy processing ethylene propylene elastomers |
US4668566A (en) | 1985-10-07 | 1987-05-26 | Kimberly-Clark Corporation | Multilayer nonwoven fabric made with poly-propylene and polyethylene |
US4701432A (en) | 1985-11-15 | 1987-10-20 | Exxon Chemical Patents Inc. | Supported polymerization catalyst |
US5084534A (en) | 1987-06-04 | 1992-01-28 | Exxon Chemical Patents, Inc. | High pressure, high temperature polymerization of ethylene |
DE3853487T2 (de) | 1987-01-19 | 1995-07-27 | Sumitomo Chemical Co | Elastische Copolymere aus Äthylen, Propylen und einem nichtconjugiertem Dien und Verwendung davon. |
US5408017A (en) | 1987-01-30 | 1995-04-18 | Exxon Chemical Patents Inc. | High temperature polymerization process using ionic catalysts to produce polyolefins |
US5264405A (en) | 1989-09-13 | 1993-11-23 | Exxon Chemical Patents Inc. | Monocyclopentadienyl titanium metal compounds for ethylene-α-olefin-copolymer production catalysts |
US5198401A (en) | 1987-01-30 | 1993-03-30 | Exxon Chemical Patents Inc. | Ionic metallocene catalyst compositions |
US5096867A (en) | 1990-06-04 | 1992-03-17 | Exxon Chemical Patents Inc. | Monocyclopentadienyl transition metal olefin polymerization catalysts |
US5241025A (en) | 1987-01-30 | 1993-08-31 | Exxon Chemical Patents Inc. | Catalyst system of enhanced productivity |
US5055438A (en) | 1989-09-13 | 1991-10-08 | Exxon Chemical Patents, Inc. | Olefin polymerization catalysts |
US5153157A (en) | 1987-01-30 | 1992-10-06 | Exxon Chemical Patents Inc. | Catalyst system of enhanced productivity |
PL276385A1 (en) | 1987-01-30 | 1989-07-24 | Exxon Chemical Patents Inc | Method for polymerization of olefines,diolefins and acetylene unsaturated compounds |
US4804794A (en) | 1987-07-13 | 1989-02-14 | Exxon Chemical Patents Inc. | Viscosity modifier polymers |
JP2573613B2 (ja) | 1987-08-14 | 1997-01-22 | 三菱化学株式会社 | エチレンの重合法 |
US5147949A (en) | 1988-03-29 | 1992-09-15 | Exxon Chemical Patents Inc. | Polymerization process using a silica gel supported metallocene-alumoxane catalyst |
US5231106A (en) | 1988-05-18 | 1993-07-27 | Novo Nordisk A/S | Azacyclic carboxylic acid derivatives and their preparation and use |
US5001205A (en) | 1988-06-16 | 1991-03-19 | Exxon Chemical Patents Inc. | Process for production of a high molecular weight ethylene α-olefin elastomer with a metallocene alumoxane catalyst |
US5229478A (en) | 1988-06-16 | 1993-07-20 | Exxon Chemical Patents Inc. | Process for production of high molecular weight EPDM elastomers using a metallocene-alumoxane catalyst system |
CA1327673C (en) | 1988-06-16 | 1994-03-08 | Sigmund Floyd | Process for production of high molecular weight epdm elastomers using a metallocene-alumoxane catalyst system |
US5229022A (en) | 1988-08-01 | 1993-07-20 | Exxon Chemical Patents Inc. | Ethylene alpha-olefin polymer substituted mono- and dicarboxylic acid dispersant additives (PT-920) |
CA2034759C (en) | 1988-08-01 | 2003-06-03 | Won R. Song | Novel ethylene alpha-olefin polymer substituted mono- and dicarboxylic acid dispersant additives |
AU615804B2 (en) * | 1988-09-30 | 1991-10-10 | Exxon Chemical Patents Inc. | Linear ethylene interpolymer blends of interpolymers having narrow molecular weight and composition distributions |
US5017665A (en) | 1989-07-25 | 1991-05-21 | Exxon Chemical Patents Inc. | Supported catalyst for 1-olefin and 1,4-diolefin copolymerization |
NZ235032A (en) * | 1989-08-31 | 1993-04-28 | Dow Chemical Co | Constrained geometry complexes of titanium, zirconium or hafnium comprising a substituted cyclopentadiene ligand; use as olefin polymerisation catalyst component |
US5057475A (en) | 1989-09-13 | 1991-10-15 | Exxon Chemical Patents Inc. | Mono-Cp heteroatom containing group IVB transition metal complexes with MAO: supported catalyst for olefin polymerization |
US5064802A (en) | 1989-09-14 | 1991-11-12 | The Dow Chemical Company | Metal complex compounds |
JP2807502B2 (ja) | 1989-10-05 | 1998-10-08 | 三井化学株式会社 | エチレン―プロピレン―ジエン系ゴム、エラストマー組成物およびその加硫ゴム |
FR2654108B1 (fr) | 1989-11-08 | 1993-08-20 | Norsolor Sa | Nouveaux caoutchoucs polyolefiniques et leur procede de preparation. |
US5519091A (en) | 1990-02-13 | 1996-05-21 | Mitsui Petrochemical Industries, Ltd. | Method for the preparation of ethylene polymer compositions |
US5149318A (en) | 1990-03-14 | 1992-09-22 | Minnesota Mining And Manufacturing Company | Quick-changeover blood handling apparatus |
MY107639A (en) | 1990-04-18 | 1996-05-30 | Mitsui Chemicals Incorporated | Process for the preparation of an ethylene copolymer and an olefin polymer, and catalyst for olefin polymeri -zation |
JP2545006B2 (ja) | 1990-07-03 | 1996-10-16 | ザ ダウ ケミカル カンパニー | 付加重合触媒 |
US5272236A (en) | 1991-10-15 | 1993-12-21 | The Dow Chemical Company | Elastic substantially linear olefin polymers |
US5189192A (en) | 1991-01-16 | 1993-02-23 | The Dow Chemical Company | Process for preparing addition polymerization catalysts via metal center oxidation |
CA2060019A1 (en) | 1991-03-04 | 1992-09-05 | Phil Marvin Stricklen | Process for producing polyolefins having a bimodal molecular weight distribution |
JP2894858B2 (ja) | 1991-04-05 | 1999-05-24 | 三井化学株式会社 | エチレン・α−オレフィン・ジエン系ゴムおよびその用途 |
JP3275211B2 (ja) | 1991-05-20 | 2002-04-15 | ザ ダウ ケミカル カンパニー | 付加重合触媒の製造方法 |
US5721185A (en) | 1991-06-24 | 1998-02-24 | The Dow Chemical Company | Homogeneous olefin polymerization catalyst by abstraction with lewis acids |
US5278272A (en) | 1991-10-15 | 1994-01-11 | The Dow Chemical Company | Elastic substantialy linear olefin polymers |
GB9125934D0 (en) | 1991-12-05 | 1992-02-05 | Exxon Chemical Patents Inc | Process for polymerising olefinic feeds under pressure |
EP0619827B1 (en) | 1991-12-30 | 1996-06-12 | The Dow Chemical Company | Ethylene interpolymer polymerizations |
DE69224287T2 (de) | 1992-01-06 | 1998-08-27 | The Dow Chemical Co., Midland, Mich. | Katalysatorzusammensetzung |
KR950014847B1 (ko) | 1992-01-23 | 1995-12-16 | 미쓰이세끼유 가가꾸고오교오 가부시끼가이샤 | 에틸렌계 공중합체의 제조방법 |
US5374696A (en) | 1992-03-26 | 1994-12-20 | The Dow Chemical Company | Addition polymerization process using stabilized reduced metal catalysts |
US5296433A (en) | 1992-04-14 | 1994-03-22 | Minnesota Mining And Manufacturing Company | Tris(pentafluorophenyl)borane complexes and catalysts derived therefrom |
BE1005795A3 (fr) | 1992-05-13 | 1994-02-01 | Solvay | Procede de polymerisation d'olefines et (co)polymeres a blocs derives d'au moins une olefine. |
US5240894A (en) | 1992-05-18 | 1993-08-31 | Exxon Chemical Patents Inc. | Method for making and using a supported metallocene catalyst system |
US5434115A (en) | 1992-05-22 | 1995-07-18 | Tosoh Corporation | Process for producing olefin polymer |
CA2117888C (en) | 1992-06-15 | 2001-05-15 | Howard William Turner | High temperature polymerization process using ionic catalysts to produce polyolefins |
WO1993025591A1 (en) | 1992-06-18 | 1993-12-23 | Spherilene S.R.L. | Process for preparing an ethylenic polymer |
WO1994000500A1 (en) | 1992-06-26 | 1994-01-06 | Exxon Chemical Patents Inc. | Solution phase polymerization process utilizing metallocene catalyst with production of olefin polymers |
NL9201970A (nl) | 1992-11-11 | 1994-06-01 | Dsm Nv | Indenylverbindingen en katalysatorcomponenten voor de polymerisatie van olefinen. |
US5464905A (en) | 1992-11-19 | 1995-11-07 | Mitsui Petrochemical Industries, Ltd. | Ethylene/α-olefin copolymer composition, graft modified ethylene/α-olefin copolymer composition, ethylene copolymer composition, and multi-stage olefin polymerization process |
DE69433347T2 (de) | 1993-01-29 | 2004-04-15 | Dow Global Technologies, Inc., Midland | Ethylen Copolymerisation |
US6313240B1 (en) | 1993-02-22 | 2001-11-06 | Tosoh Corporation | Process for producing ethylene/α-olefin copolymer |
US5470993A (en) | 1993-06-24 | 1995-11-28 | The Dow Chemical Company | Titanium(II) or zirconium(II) complexes and addition polymerization catalysts therefrom |
NZ268270A (en) | 1993-06-24 | 1997-10-24 | Dow Chemical Co | Titanium (ii)- or zirconium (ii)- containing complexes and addition polymerisation catalysts therefrom (m is ti or zr) |
US5372682A (en) | 1993-06-24 | 1994-12-13 | The Dow Chemical Company | Electrochemical preparation of addition polymerization catalysts |
WO1995016716A1 (en) | 1993-12-14 | 1995-06-22 | Exxon Chemical Patents Inc. | Process for producing elastomers with an indenyl metallocene catalyst system |
BR9500663A (pt) | 1994-02-17 | 1995-10-31 | Union Carbide Chem Plastic | Composição de catalisador processo de preparação de uma composição de catalisador e processo para a produção de homopolímeros ou copolímeros de etileno |
US5486632A (en) | 1994-06-28 | 1996-01-23 | The Dow Chemical Company | Group 4 metal diene complexes and addition polymerization catalysts therefrom |
DE4432798A1 (de) | 1994-09-15 | 1996-03-21 | Basf Ag | Hochflexible Propylen-Ethylen-Copolymerisate |
US5677382A (en) | 1994-12-19 | 1997-10-14 | Japan Synthetic Rubber Co., Ltd. | Ethylene-α-olefin-non-conjugated diene copolymer rubber composition |
TW383314B (en) | 1994-12-20 | 2000-03-01 | Mitsui Petrochemical Ind | Ethylene-alpha-olefin-nonconjugated polyene random copolymer, rubber composition, and process for preparing the random copolymer |
US5696213A (en) | 1995-04-21 | 1997-12-09 | Exxon Chemical Patents Inc. | Ethylene-α-olefin-diolefin elastomers solution polymerization process |
EP0743066A3 (en) | 1995-05-16 | 1998-09-30 | Mitsui Pharmaceuticals, Inc. | Wound-healing agent |
-
1996
- 1996-07-12 US US08/679,538 patent/US6545088B1/en not_active Expired - Lifetime
-
1997
- 1997-07-09 CZ CZ9994A patent/CZ9499A3/cs unknown
- 1997-07-09 CA CA002256668A patent/CA2256668C/en not_active Expired - Lifetime
- 1997-07-09 KR KR10-1999-7000204A patent/KR100496101B1/ko not_active IP Right Cessation
- 1997-07-09 ES ES97934156T patent/ES2156001T3/es not_active Expired - Lifetime
- 1997-07-09 HU HU9904354A patent/HUP9904354A3/hu unknown
- 1997-07-09 WO PCT/US1997/012294 patent/WO1998002471A1/en active IP Right Grant
- 1997-07-09 NZ NZ332880A patent/NZ332880A/xx unknown
- 1997-07-09 PL PL97331038A patent/PL331038A1/xx unknown
- 1997-07-09 JP JP10506243A patent/JP2000514857A/ja active Pending
- 1997-07-09 AT AT97934156T patent/ATE200680T1/de active
- 1997-07-09 AU AU37279/97A patent/AU718342B2/en not_active Ceased
- 1997-07-09 TR TR1999/00050T patent/TR199900050T2/xx unknown
- 1997-07-09 EP EP97934156A patent/EP0910593B1/en not_active Expired - Lifetime
- 1997-07-09 CN CN97195993A patent/CN1098289C/zh not_active Expired - Lifetime
- 1997-07-09 BR BR9710347A patent/BR9710347A/pt not_active Application Discontinuation
- 1997-07-09 DE DE69704617T patent/DE69704617T2/de not_active Expired - Lifetime
- 1997-07-11 TW TW086109819A patent/TW341576B/zh active
-
1999
- 1999-01-11 NO NO990095A patent/NO990095L/no not_active Application Discontinuation
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2002528610A (ja) * | 1998-11-02 | 2002-09-03 | デュポン ダウ エラストマーズ エルエルシー | 剪断減粘性エチレン/α−オレフィンインターポリマーおよびそれらの製造法 |
JP2003507541A (ja) * | 1999-08-19 | 2003-02-25 | デユポン・ダウ・エラストマーズ・エル・エル・シー | 幅広い分子量分布を示すポリマーブレンド物を単一の反応槽内で製造する方法 |
JP2008516068A (ja) * | 2004-10-13 | 2008-05-15 | エクソンモービル・ケミカル・パテンツ・インク | エラストマー性反応ブレンド組成物 |
JP2008525546A (ja) * | 2004-12-23 | 2008-07-17 | ボレアリス テクノロジー オイ | コポリマー |
JP2011529522A (ja) * | 2008-07-29 | 2011-12-08 | アルケマ フランス | 再生可能な材料からのグラフト化ポリエチレンの製造、得られるポリエチレン、およびその使用 |
JP2012533653A (ja) * | 2009-07-15 | 2012-12-27 | ダウ グローバル テクノロジーズ エルエルシー | ポリマー組成物、その製造方法及びそれから製造される物品 |
JP2015521692A (ja) * | 2012-08-31 | 2015-07-30 | エクソンモービル ケミカル パテンツ インコーポレイテッド | ポリマーを形成するためのプラントおよび方法 |
JP2016164284A (ja) * | 2012-08-31 | 2016-09-08 | エクソンモービル ケミカル パテンツ インコーポレイテッド | ポリマーを形成するためのプラントおよび方法 |
Also Published As
Publication number | Publication date |
---|---|
CN1223670A (zh) | 1999-07-21 |
TW341576B (en) | 1998-10-01 |
KR100496101B1 (ko) | 2005-06-17 |
AU3727997A (en) | 1998-02-09 |
TR199900050T2 (xx) | 1999-03-22 |
DE69704617T2 (de) | 2001-08-02 |
DE69704617D1 (de) | 2001-05-23 |
CA2256668C (en) | 2006-08-22 |
HUP9904354A2 (hu) | 2000-04-28 |
CA2256668A1 (en) | 1998-01-22 |
PL331038A1 (en) | 1999-06-21 |
CZ9499A3 (cs) | 1999-03-17 |
NZ332880A (en) | 2000-07-28 |
BR9710347A (pt) | 1999-08-17 |
ATE200680T1 (de) | 2001-05-15 |
NO990095L (no) | 1999-01-12 |
KR20000023740A (ko) | 2000-04-25 |
EP0910593B1 (en) | 2001-04-18 |
EP0910593A1 (en) | 1999-04-28 |
HUP9904354A3 (en) | 2000-05-29 |
US6545088B1 (en) | 2003-04-08 |
CN1098289C (zh) | 2003-01-08 |
AU718342B2 (en) | 2000-04-13 |
NO990095D0 (no) | 1999-01-11 |
ES2156001T3 (es) | 2001-06-01 |
WO1998002471A1 (en) | 1998-01-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP2000514857A (ja) | 弾性重合体およびそれの製造方法 | |
US5814714A (en) | Mono-olefin/polyene interpolymers, method of preparation, compositions containing the same, and articles made thereof | |
JP6039906B2 (ja) | 剪断減粘性エチレン/α−オレフィンインターポリマーおよびそれらの製造法 | |
EP0898585B1 (en) | Polyolefin composition with molecular weight maximum occuring in that part of the composition that has the highest comonomer content | |
JP6165685B2 (ja) | 幅広い分子量分布を示すポリマーブレンド物を単一の反応槽内で製造する方法 | |
KR100554775B1 (ko) | 가교결합된 하프노센 화합물을 사용하는 올레핀공중합체의 중합방법 | |
KR100691576B1 (ko) | 초고분자량 에틸렌계 중합체 | |
JP2001506260A (ja) | 3―アリール置換インデニル含有金属錯体及び重合方法 | |
JPH09502761A (ja) | オレフィン類の気相重合 | |
JP4868853B2 (ja) | 超高分子量エチレン系重合体 | |
JP2001522399A (ja) | 置換インデニル含有金属錯体を用いて生じさせたオレフィンポリマー類 | |
KR100490509B1 (ko) | 공단량체함량이가장높은부분에서분자량이최대인폴리올레핀조성물 | |
CZ375899A3 (cs) | Olefinové polymery připravené s kovovými komplexy obsahujícími substituovaný indenyl |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20040618 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20060221 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20050926 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20060519 |
|
A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20060703 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20060629 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20060905 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20061201 |
|
A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20070122 |
|
A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20070522 |