JP5348732B2 - オレフィン重合およびそれにより生成されるポリマーのための多種触媒および反応装置システム - Google Patents
オレフィン重合およびそれにより生成されるポリマーのための多種触媒および反応装置システム Download PDFInfo
- Publication number
- JP5348732B2 JP5348732B2 JP2007508539A JP2007508539A JP5348732B2 JP 5348732 B2 JP5348732 B2 JP 5348732B2 JP 2007508539 A JP2007508539 A JP 2007508539A JP 2007508539 A JP2007508539 A JP 2007508539A JP 5348732 B2 JP5348732 B2 JP 5348732B2
- Authority
- JP
- Japan
- Prior art keywords
- rac
- zrme
- activated
- indenyl
- boron
- 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.)
- Expired - Fee Related
Links
- 239000003054 catalyst Substances 0.000 title claims abstract description 389
- 229920000642 polymer Polymers 0.000 title claims abstract description 311
- 150000001336 alkenes Chemical class 0.000 title claims abstract description 76
- 238000006116 polymerization reaction Methods 0.000 title claims description 91
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 title claims description 33
- 238000006243 chemical reaction Methods 0.000 claims abstract description 179
- 239000012190 activator Substances 0.000 claims abstract description 145
- 238000000034 method Methods 0.000 claims abstract description 109
- 230000008569 process Effects 0.000 claims abstract description 59
- -1 2-methyl-4-phenyl indenyl Chemical group 0.000 claims description 962
- 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 claims description 160
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 claims description 138
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 claims description 132
- 150000001875 compounds Chemical class 0.000 claims description 131
- ZOICEQJZAWJHSI-UHFFFAOYSA-N (2,3,4,5,6-pentafluorophenyl)boron Chemical compound [B]C1=C(F)C(F)=C(F)C(F)=C1F ZOICEQJZAWJHSI-UHFFFAOYSA-N 0.000 claims description 112
- 239000005977 Ethylene Substances 0.000 claims description 100
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 98
- 229910007926 ZrCl Inorganic materials 0.000 claims description 97
- 150000001450 anions Chemical class 0.000 claims description 95
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 75
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 71
- JLTDJTHDQAWBAV-UHFFFAOYSA-O dimethyl(phenyl)azanium Chemical compound C[NH+](C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-O 0.000 claims description 62
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 claims description 40
- 229920000098 polyolefin Polymers 0.000 claims description 35
- 239000012968 metallocene catalyst Substances 0.000 claims description 34
- ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 claims description 30
- 239000002002 slurry Substances 0.000 claims description 26
- 238000004519 manufacturing process Methods 0.000 claims description 25
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 claims description 22
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims description 19
- 230000004913 activation Effects 0.000 claims description 18
- 239000012071 phase Substances 0.000 claims description 18
- 229910052796 boron Inorganic materials 0.000 claims description 16
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 13
- 125000000129 anionic group Chemical group 0.000 claims description 13
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 claims description 12
- 239000003795 chemical substances by application Substances 0.000 claims description 11
- 230000000707 stereoselective effect Effects 0.000 claims description 11
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 claims description 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 9
- 230000003213 activating effect Effects 0.000 claims description 7
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 7
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 claims description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- AFFLGGQVNFXPEV-UHFFFAOYSA-N n-decene Natural products CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 claims description 5
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1 -dodecene Natural products CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 claims description 4
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims description 4
- 229940069096 dodecene Drugs 0.000 claims description 4
- 239000007791 liquid phase Substances 0.000 claims description 3
- 125000000538 pentafluorophenyl group Chemical group FC1=C(F)C(F)=C(*)C(F)=C1F 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 abstract description 19
- 229910052726 zirconium Inorganic materials 0.000 description 197
- VPGLGRNSAYHXPY-UHFFFAOYSA-L zirconium(2+);dichloride Chemical compound Cl[Zr]Cl VPGLGRNSAYHXPY-UHFFFAOYSA-L 0.000 description 177
- 239000003446 ligand Substances 0.000 description 120
- 229910052735 hafnium Inorganic materials 0.000 description 103
- 239000000178 monomer Substances 0.000 description 103
- 239000000203 mixture Substances 0.000 description 84
- KUNZSLJMPCDOGI-UHFFFAOYSA-L [Cl-].[Cl-].[Hf+2] Chemical compound [Cl-].[Cl-].[Hf+2] KUNZSLJMPCDOGI-UHFFFAOYSA-L 0.000 description 81
- AQZWEFBJYQSQEH-UHFFFAOYSA-N 2-methyloxaluminane Chemical compound C[Al]1CCCCO1 AQZWEFBJYQSQEH-UHFFFAOYSA-N 0.000 description 74
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 61
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 59
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 58
- 239000000243 solution Substances 0.000 description 58
- 239000010936 titanium Chemical group 0.000 description 55
- 229910052719 titanium Chemical group 0.000 description 50
- 239000004743 Polypropylene Substances 0.000 description 49
- 229920001155 polypropylene Polymers 0.000 description 49
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 48
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 45
- ZWYDDDAMNQQZHD-UHFFFAOYSA-L titanium(ii) chloride Chemical compound [Cl-].[Cl-].[Ti+2] ZWYDDDAMNQQZHD-UHFFFAOYSA-L 0.000 description 45
- 150000001993 dienes Chemical class 0.000 description 41
- 229910052723 transition metal Inorganic materials 0.000 description 41
- 229910052751 metal Inorganic materials 0.000 description 40
- 239000002904 solvent Substances 0.000 description 40
- 230000001070 adhesive effect Effects 0.000 description 38
- 239000000853 adhesive Substances 0.000 description 37
- 239000002184 metal Substances 0.000 description 35
- 150000003624 transition metals Chemical class 0.000 description 35
- 125000001424 substituent group Chemical group 0.000 description 31
- 150000003623 transition metal compounds Chemical class 0.000 description 30
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 26
- 239000012041 precatalyst Substances 0.000 description 26
- 229920001577 copolymer Polymers 0.000 description 25
- 239000000758 substrate Substances 0.000 description 25
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 24
- 125000004432 carbon atom Chemical group C* 0.000 description 23
- 239000004711 α-olefin Substances 0.000 description 23
- 239000011347 resin Substances 0.000 description 22
- 229920005989 resin Polymers 0.000 description 22
- 125000003118 aryl group Chemical group 0.000 description 21
- 239000012634 fragment Substances 0.000 description 21
- 125000001183 hydrocarbyl group Chemical group 0.000 description 21
- 229910052752 metalloid Inorganic materials 0.000 description 20
- 239000000047 product Substances 0.000 description 20
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 20
- 239000001993 wax Substances 0.000 description 20
- 229910052782 aluminium Inorganic materials 0.000 description 19
- 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 18
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 18
- 150000001768 cations Chemical class 0.000 description 18
- 239000001257 hydrogen Substances 0.000 description 18
- 229910052739 hydrogen Inorganic materials 0.000 description 18
- 239000007788 liquid Substances 0.000 description 18
- 238000002156 mixing Methods 0.000 description 18
- 230000007935 neutral effect Effects 0.000 description 18
- 229920002554 vinyl polymer Polymers 0.000 description 18
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 17
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 17
- 239000000835 fiber Substances 0.000 description 17
- 230000009021 linear effect Effects 0.000 description 17
- 238000002844 melting Methods 0.000 description 17
- 230000008018 melting Effects 0.000 description 17
- 150000003254 radicals Chemical class 0.000 description 17
- 238000001816 cooling Methods 0.000 description 16
- 229920001971 elastomer Polymers 0.000 description 16
- 229910052757 nitrogen Inorganic materials 0.000 description 16
- 239000000654 additive Substances 0.000 description 15
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 14
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 14
- HFKJQIJFRMRSKM-UHFFFAOYSA-N [3,5-bis(trifluoromethyl)phenoxy]boronic acid Chemical compound OB(O)OC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 HFKJQIJFRMRSKM-UHFFFAOYSA-N 0.000 description 14
- 125000004122 cyclic group Chemical group 0.000 description 14
- 230000004927 fusion Effects 0.000 description 14
- 238000001542 size-exclusion chromatography Methods 0.000 description 14
- 241000894007 species Species 0.000 description 14
- NMLGKEDSNASIHM-UHFFFAOYSA-N (2,3,4,5,6,7,8-heptafluoronaphthalen-1-yl)oxyboronic acid Chemical compound FC1=C(F)C(F)=C2C(OB(O)O)=C(F)C(F)=C(F)C2=C1F NMLGKEDSNASIHM-UHFFFAOYSA-N 0.000 description 13
- 239000002841 Lewis acid Substances 0.000 description 13
- 125000004429 atom Chemical group 0.000 description 13
- 150000002738 metalloids Chemical class 0.000 description 13
- 230000000737 periodic effect Effects 0.000 description 13
- 239000002516 radical scavenger Substances 0.000 description 13
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 12
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 12
- 229920006125 amorphous polymer Polymers 0.000 description 12
- 238000010924 continuous production Methods 0.000 description 12
- 150000007517 lewis acids Chemical class 0.000 description 12
- 239000002243 precursor Substances 0.000 description 12
- 229910052736 halogen Inorganic materials 0.000 description 11
- 125000005842 heteroatom Chemical group 0.000 description 11
- 239000000463 material Substances 0.000 description 11
- 229920002959 polymer blend Polymers 0.000 description 11
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 10
- 239000002879 Lewis base Substances 0.000 description 10
- 238000005481 NMR spectroscopy Methods 0.000 description 10
- 239000002253 acid Substances 0.000 description 10
- 150000008064 anhydrides Chemical group 0.000 description 10
- 230000015572 biosynthetic process Effects 0.000 description 10
- 239000012018 catalyst precursor Substances 0.000 description 10
- 239000002131 composite material Substances 0.000 description 10
- 150000007527 lewis bases Chemical class 0.000 description 10
- 239000003921 oil Substances 0.000 description 10
- 239000000126 substance Substances 0.000 description 10
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 9
- 239000000969 carrier Substances 0.000 description 9
- 125000002091 cationic group Chemical group 0.000 description 9
- 238000002425 crystallisation Methods 0.000 description 9
- 230000008025 crystallization Effects 0.000 description 9
- 239000003085 diluting agent Substances 0.000 description 9
- 230000000694 effects Effects 0.000 description 9
- 150000002148 esters Chemical class 0.000 description 9
- 150000002367 halogens Chemical group 0.000 description 9
- 229920001519 homopolymer Polymers 0.000 description 9
- 125000002524 organometallic group Chemical group 0.000 description 9
- 230000003068 static effect Effects 0.000 description 9
- JLTRXTDYQLMHGR-UHFFFAOYSA-N trimethylaluminium Chemical compound C[Al](C)C JLTRXTDYQLMHGR-UHFFFAOYSA-N 0.000 description 9
- OLFPYUPGPBITMH-UHFFFAOYSA-N tritylium Chemical compound C1=CC=CC=C1[C+](C=1C=CC=CC=1)C1=CC=CC=C1 OLFPYUPGPBITMH-UHFFFAOYSA-N 0.000 description 9
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 8
- 125000000217 alkyl group Chemical group 0.000 description 8
- OJOSABWCUVCSTQ-UHFFFAOYSA-N cyclohepta-2,4,6-trienylium Chemical compound C1=CC=C[CH+]=C[CH]1 OJOSABWCUVCSTQ-UHFFFAOYSA-N 0.000 description 8
- 239000000806 elastomer Substances 0.000 description 8
- 239000007789 gas Substances 0.000 description 8
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 8
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N methylene hexane Natural products CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 8
- 230000000379 polymerizing effect Effects 0.000 description 8
- 239000005060 rubber Substances 0.000 description 8
- 229910052710 silicon Inorganic materials 0.000 description 8
- 235000007586 terpenes Nutrition 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 7
- 239000007848 Bronsted acid Substances 0.000 description 7
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 7
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 7
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical group [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 7
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical group [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 7
- 150000004703 alkoxides Chemical class 0.000 description 7
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 7
- 229910052798 chalcogen Inorganic materials 0.000 description 7
- 150000004820 halides Chemical class 0.000 description 7
- 150000004678 hydrides Chemical class 0.000 description 7
- 239000000123 paper Substances 0.000 description 7
- 229910052698 phosphorus Inorganic materials 0.000 description 7
- 229920013639 polyalphaolefin Polymers 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- 239000010703 silicon Substances 0.000 description 7
- 238000006467 substitution reaction Methods 0.000 description 7
- 229910052717 sulfur Inorganic materials 0.000 description 7
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 7
- MCULRUJILOGHCJ-UHFFFAOYSA-N triisobutylaluminium Chemical compound CC(C)C[Al](CC(C)C)CC(C)C MCULRUJILOGHCJ-UHFFFAOYSA-N 0.000 description 7
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 6
- 239000004215 Carbon black (E152) Substances 0.000 description 6
- OKTJSMMVPCPJKN-OUBTZVSYSA-N Carbon-13 Chemical compound [13C] OKTJSMMVPCPJKN-OUBTZVSYSA-N 0.000 description 6
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 6
- 150000001408 amides Chemical class 0.000 description 6
- 150000001721 carbon Chemical group 0.000 description 6
- LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 description 6
- 239000012954 diazonium Substances 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-O diazynium Chemical compound [NH+]#N IJGRMHOSHXDMSA-UHFFFAOYSA-O 0.000 description 6
- 238000009826 distribution Methods 0.000 description 6
- 229910052732 germanium Inorganic materials 0.000 description 6
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 6
- 239000011521 glass Substances 0.000 description 6
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 6
- 229930195733 hydrocarbon Natural products 0.000 description 6
- 238000003475 lamination Methods 0.000 description 6
- 238000005259 measurement Methods 0.000 description 6
- 150000002736 metal compounds Chemical class 0.000 description 6
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 238000005453 pelletization Methods 0.000 description 6
- 239000011574 phosphorus Substances 0.000 description 6
- 229910052696 pnictogen Inorganic materials 0.000 description 6
- 229920001083 polybutene Polymers 0.000 description 6
- 239000002685 polymerization catalyst Substances 0.000 description 6
- 239000000377 silicon dioxide Substances 0.000 description 6
- 150000003505 terpenes Chemical class 0.000 description 6
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 6
- LFXVBWRMVZPLFK-UHFFFAOYSA-N trioctylalumane Chemical compound CCCCCCCC[Al](CCCCCCCC)CCCCCCCC LFXVBWRMVZPLFK-UHFFFAOYSA-N 0.000 description 6
- 229910052720 vanadium Inorganic materials 0.000 description 6
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 229920000181 Ethylene propylene rubber Polymers 0.000 description 5
- IGCCPSZEERPJNE-UHFFFAOYSA-L [Cl-].[Cl-].C1CC2CC=CC=C2C1[Hf+2]([SiH](C)C)C1C2=CC=CCC2CC1 Chemical compound [Cl-].[Cl-].C1CC2CC=CC=C2C1[Hf+2]([SiH](C)C)C1C2=CC=CCC2CC1 IGCCPSZEERPJNE-UHFFFAOYSA-L 0.000 description 5
- RLEZACANRPOGPQ-UHFFFAOYSA-L [Cl-].[Cl-].C1CC2CC=CC=C2C1[Zr+2]([SiH](C)C)C1C2=CC=CCC2CC1 Chemical compound [Cl-].[Cl-].C1CC2CC=CC=C2C1[Zr+2]([SiH](C)C)C1C2=CC=CCC2CC1 RLEZACANRPOGPQ-UHFFFAOYSA-L 0.000 description 5
- 125000001931 aliphatic group Chemical group 0.000 description 5
- 239000003963 antioxidant agent Substances 0.000 description 5
- BTZMQCSTZIUDIY-UHFFFAOYSA-N boric acid 1,2,3,4,5-pentafluoro-6-(2,3,4,5,6-pentafluorophenyl)benzene Chemical compound OB(O)O.FC1=C(F)C(F)=C(F)C(F)=C1C1=C(F)C(F)=C(F)C(F)=C1F.FC1=C(F)C(F)=C(F)C(F)=C1C1=C(F)C(F)=C(F)C(F)=C1F.FC1=C(F)C(F)=C(F)C(F)=C1C1=C(F)C(F)=C(F)C(F)=C1F.FC1=C(F)C(F)=C(F)C(F)=C1C1=C(F)C(F)=C(F)C(F)=C1F BTZMQCSTZIUDIY-UHFFFAOYSA-N 0.000 description 5
- 238000004132 cross linking Methods 0.000 description 5
- 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 5
- NLDGJRWPPOSWLC-UHFFFAOYSA-N deca-1,9-diene Chemical compound C=CCCCCCCC=C NLDGJRWPPOSWLC-UHFFFAOYSA-N 0.000 description 5
- 238000000113 differential scanning calorimetry Methods 0.000 description 5
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 238000005227 gel permeation chromatography Methods 0.000 description 5
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical group [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 238000010348 incorporation Methods 0.000 description 5
- 229920002521 macromolecule Polymers 0.000 description 5
- 239000003607 modifier Substances 0.000 description 5
- 239000012299 nitrogen atmosphere Substances 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- 239000004014 plasticizer Substances 0.000 description 5
- 239000011148 porous material Substances 0.000 description 5
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 5
- 238000001374 small-angle light scattering Methods 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 229920001576 syndiotactic polymer Polymers 0.000 description 5
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 5
- XWJBRBSPAODJER-UHFFFAOYSA-N 1,7-octadiene Chemical compound C=CCCCCC=C XWJBRBSPAODJER-UHFFFAOYSA-N 0.000 description 4
- GQEZCXVZFLOKMC-UHFFFAOYSA-N 1-hexadecene Chemical compound CCCCCCCCCCCCCCC=C GQEZCXVZFLOKMC-UHFFFAOYSA-N 0.000 description 4
- DCTOHCCUXLBQMS-UHFFFAOYSA-N 1-undecene Chemical compound CCCCCCCCCC=C DCTOHCCUXLBQMS-UHFFFAOYSA-N 0.000 description 4
- JTXUVHFRSRTSAT-UHFFFAOYSA-N 3,5,5-trimethylhex-1-ene Chemical compound C=CC(C)CC(C)(C)C JTXUVHFRSRTSAT-UHFFFAOYSA-N 0.000 description 4
- LDTAOIUHUHHCMU-UHFFFAOYSA-N 3-methylpent-1-ene Chemical compound CCC(C)C=C LDTAOIUHUHHCMU-UHFFFAOYSA-N 0.000 description 4
- PNZJHMTVFFXLAX-UHFFFAOYSA-N C1=CC2=CC=CC=C2C1[Hf]([SiH](C)C)C1C2=CC=CC=C2C=C1 Chemical compound C1=CC2=CC=CC=C2C1[Hf]([SiH](C)C)C1C2=CC=CC=C2C=C1 PNZJHMTVFFXLAX-UHFFFAOYSA-N 0.000 description 4
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 4
- 239000004698 Polyethylene Substances 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 4
- FJMJPZLXUXRLLD-UHFFFAOYSA-L [Cl-].[Cl-].C1=CC2=CC=CC=C2C1[Zr+2]([SiH](C)C)C1C2=CC=CC=C2C=C1 Chemical compound [Cl-].[Cl-].C1=CC2=CC=CC=C2C1[Zr+2]([SiH](C)C)C1C2=CC=CC=C2C=C1 FJMJPZLXUXRLLD-UHFFFAOYSA-L 0.000 description 4
- LEOYKWIXWJXYQJ-UHFFFAOYSA-L [Cl-].[Cl-].CC1=CC2=CC=CC=C2C1[Zr+2]([SiH](C)C)C1C2=CC=CC=C2C=C1C Chemical compound [Cl-].[Cl-].CC1=CC2=CC=CC=C2C1[Zr+2]([SiH](C)C)C1C2=CC=CC=C2C=C1C LEOYKWIXWJXYQJ-UHFFFAOYSA-L 0.000 description 4
- HWESFSSIAPADSJ-UHFFFAOYSA-L [Cl-].[Cl-].C[SiH](C)[Hf++](C1C=Cc2c1c(C)ccc2C)C1C=Cc2c1c(C)ccc2C Chemical compound [Cl-].[Cl-].C[SiH](C)[Hf++](C1C=Cc2c1c(C)ccc2C)C1C=Cc2c1c(C)ccc2C HWESFSSIAPADSJ-UHFFFAOYSA-L 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 125000003342 alkenyl group Chemical group 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- 229920013640 amorphous poly alpha olefin Polymers 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- ZHFFGBNOSGNGDM-UHFFFAOYSA-N carbanide hafnium(4+) inden-3a-id-1-yl-inden-1-id-1-yl-dimethylsilane Chemical group [CH3-].[CH3-].[Hf+4].C[Si](C)([c-]1ccc2ccccc12)[c-]1ccc2ccccc12 ZHFFGBNOSGNGDM-UHFFFAOYSA-N 0.000 description 4
- 238000012512 characterization method Methods 0.000 description 4
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 4
- IDASTKMEQGPVRR-UHFFFAOYSA-N cyclopenta-1,3-diene;zirconium(2+) Chemical compound [Zr+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 IDASTKMEQGPVRR-UHFFFAOYSA-N 0.000 description 4
- 229910000071 diazene Inorganic materials 0.000 description 4
- GGSUCNLOZRCGPQ-UHFFFAOYSA-O diethyl(phenyl)azanium Chemical compound CC[NH+](CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-O 0.000 description 4
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 4
- 239000010408 film Substances 0.000 description 4
- 230000006870 function Effects 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 239000002198 insoluble material Substances 0.000 description 4
- 239000001282 iso-butane Substances 0.000 description 4
- 229910052747 lanthanoid Inorganic materials 0.000 description 4
- 150000002602 lanthanoids Chemical class 0.000 description 4
- JZBZLRKFJWQZHU-UHFFFAOYSA-N n,n,2,4,6-pentamethylaniline Chemical compound CN(C)C1=C(C)C=C(C)C=C1C JZBZLRKFJWQZHU-UHFFFAOYSA-N 0.000 description 4
- 125000001624 naphthyl group Chemical group 0.000 description 4
- VJHGSLHHMIELQD-UHFFFAOYSA-N nona-1,8-diene Chemical compound C=CCCCCCC=C VJHGSLHHMIELQD-UHFFFAOYSA-N 0.000 description 4
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 4
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 239000007800 oxidant agent Substances 0.000 description 4
- 238000004806 packaging method and process Methods 0.000 description 4
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 229920005606 polypropylene copolymer Polymers 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 238000000638 solvent extraction Methods 0.000 description 4
- 239000011593 sulfur Substances 0.000 description 4
- 239000000454 talc Substances 0.000 description 4
- 229910052623 talc Inorganic materials 0.000 description 4
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Chemical group OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 4
- 238000012546 transfer Methods 0.000 description 4
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 4
- ZMANZCXQSJIPKH-UHFFFAOYSA-O triethylammonium ion Chemical compound CC[NH+](CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-O 0.000 description 4
- CXKQHHJKHZXXPZ-UHFFFAOYSA-N triethylsilanylium Chemical compound CC[Si+](CC)CC CXKQHHJKHZXXPZ-UHFFFAOYSA-N 0.000 description 4
- RIOQSEWOXXDEQQ-UHFFFAOYSA-O triphenylphosphanium Chemical compound C1=CC=CC=C1[PH+](C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-O 0.000 description 4
- OJOWICOBYCXEKR-KRXBUXKQSA-N (5e)-5-ethylidenebicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(=C/C)/CC1C=C2 OJOWICOBYCXEKR-KRXBUXKQSA-N 0.000 description 3
- 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 3
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical compound CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 3
- INYHZQLKOKTDAI-UHFFFAOYSA-N 5-ethenylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(C=C)CC1C=C2 INYHZQLKOKTDAI-UHFFFAOYSA-N 0.000 description 3
- 239000004322 Butylated hydroxytoluene Substances 0.000 description 3
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 3
- ORLOFKMUOFCWGQ-UHFFFAOYSA-N CC1=C(C(C=C2)[Hf](C)(C3C4=C(C)C=CC(C)=C4C=C3)[SiH2]C3=CC=CC=C3)C2=C(C)C=C1.Cl.Cl Chemical compound CC1=C(C(C=C2)[Hf](C)(C3C4=C(C)C=CC(C)=C4C=C3)[SiH2]C3=CC=CC=C3)C2=C(C)C=C1.Cl.Cl ORLOFKMUOFCWGQ-UHFFFAOYSA-N 0.000 description 3
- UCSPDPQSCVXVHY-UHFFFAOYSA-N CC1=C(C(C=C2)[Zr](C)(C3C4=C(C)C=CC(C)=C4C=C3)[SiH2]C3=CC=CC=C3)C2=C(C)C=C1.Cl.Cl Chemical compound CC1=C(C(C=C2)[Zr](C)(C3C4=C(C)C=CC(C)=C4C=C3)[SiH2]C3=CC=CC=C3)C2=C(C)C=C1.Cl.Cl UCSPDPQSCVXVHY-UHFFFAOYSA-N 0.000 description 3
- XLCYGAPESVMMLC-UHFFFAOYSA-L CC1=CC(C(=CC=C2)C=3C=CC=CC=3)=C2C1[Hf](Cl)(Cl)([SiH](C)C)C1C(C)=CC2=C1C=CC=C2C1=CC=CC=C1 Chemical compound CC1=CC(C(=CC=C2)C=3C=CC=CC=3)=C2C1[Hf](Cl)(Cl)([SiH](C)C)C1C(C)=CC2=C1C=CC=C2C1=CC=CC=C1 XLCYGAPESVMMLC-UHFFFAOYSA-L 0.000 description 3
- XKSFSOKJDSMNPI-UHFFFAOYSA-N C[Hf](C1C2=CC=CC=C2C=C1)(C1C2=CC=CC=C2C=C1)[SiH2]C1=CC=CC=C1.Cl.Cl Chemical compound C[Hf](C1C2=CC=CC=C2C=C1)(C1C2=CC=CC=C2C=C1)[SiH2]C1=CC=CC=C1.Cl.Cl XKSFSOKJDSMNPI-UHFFFAOYSA-N 0.000 description 3
- IJCJZGOYNJFVFH-UHFFFAOYSA-N C[Hf](C1C2=CC=CCC2CC1)(C1C2=CC=CCC2CC1)[SiH2]C1=CC=CC=C1.Cl.Cl Chemical compound C[Hf](C1C2=CC=CCC2CC1)(C1C2=CC=CCC2CC1)[SiH2]C1=CC=CC=C1.Cl.Cl IJCJZGOYNJFVFH-UHFFFAOYSA-N 0.000 description 3
- FPUALFQZGDMNAT-UHFFFAOYSA-N C[Zr](C1C2=CC=CC=C2C=C1)(C1C2=CC=CC=C2C=C1)[SiH2]C1=CC=CC=C1.Cl.Cl Chemical compound C[Zr](C1C2=CC=CC=C2C=C1)(C1C2=CC=CC=C2C=C1)[SiH2]C1=CC=CC=C1.Cl.Cl FPUALFQZGDMNAT-UHFFFAOYSA-N 0.000 description 3
- 239000004971 Cross linker Substances 0.000 description 3
- 229920002943 EPDM rubber Polymers 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 239000004831 Hot glue Substances 0.000 description 3
- 239000013032 Hydrocarbon resin Substances 0.000 description 3
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 3
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Chemical group OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- BWUKAWLFMALYIV-UHFFFAOYSA-L [Cl-].[Cl-].C1=CC2=CC=CC=C2C1[Hf+2](C1C2=CC=CC=C2C=C1)[SiH](C=1C=CC=CC=1)C1=CC=CC=C1 Chemical compound [Cl-].[Cl-].C1=CC2=CC=CC=C2C1[Hf+2](C1C2=CC=CC=C2C=C1)[SiH](C=1C=CC=CC=1)C1=CC=CC=C1 BWUKAWLFMALYIV-UHFFFAOYSA-L 0.000 description 3
- SGJOMARGPMMNKC-UHFFFAOYSA-L [Cl-].[Cl-].C1=CC2=CC=CC=C2C1[Hf+2]([SiH](C)C)C1C2=CC=CC=C2C=C1 Chemical compound [Cl-].[Cl-].C1=CC2=CC=CC=C2C1[Hf+2]([SiH](C)C)C1C2=CC=CC=C2C=C1 SGJOMARGPMMNKC-UHFFFAOYSA-L 0.000 description 3
- DHOIFLAXQKMNNF-UHFFFAOYSA-L [Cl-].[Cl-].C1=CC2=CC=CC=C2C1[Zr+2](C1C2=CC=CC=C2C=C1)[SiH](C=1C=CC=CC=1)C1=CC=CC=C1 Chemical compound [Cl-].[Cl-].C1=CC2=CC=CC=C2C1[Zr+2](C1C2=CC=CC=C2C=C1)[SiH](C=1C=CC=CC=1)C1=CC=CC=C1 DHOIFLAXQKMNNF-UHFFFAOYSA-L 0.000 description 3
- OYKIBEVXOHBLAP-UHFFFAOYSA-L [Cl-].[Cl-].CC1=CC2=CC=CC=C2C1[Hf+2]([SiH](C)C)C1C2=CC=CC=C2C=C1C Chemical compound [Cl-].[Cl-].CC1=CC2=CC=CC=C2C1[Hf+2]([SiH](C)C)C1C2=CC=CC=C2C=C1C OYKIBEVXOHBLAP-UHFFFAOYSA-L 0.000 description 3
- PCRVPTVYRLHWKZ-UHFFFAOYSA-L [Cl-].[Cl-].Cc1ccc(C)c2C(C=Cc12)[Zr++](C1C=Cc2c1c(C)ccc2C)[SiH](c1ccccc1)c1ccccc1 Chemical compound [Cl-].[Cl-].Cc1ccc(C)c2C(C=Cc12)[Zr++](C1C=Cc2c1c(C)ccc2C)[SiH](c1ccccc1)c1ccccc1 PCRVPTVYRLHWKZ-UHFFFAOYSA-L 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 229910052768 actinide Inorganic materials 0.000 description 3
- 150000001255 actinides Chemical class 0.000 description 3
- 125000002015 acyclic group Chemical group 0.000 description 3
- 150000001335 aliphatic alkanes Chemical class 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 239000011324 bead Substances 0.000 description 3
- 230000002902 bimodal effect Effects 0.000 description 3
- 238000007664 blowing Methods 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- UORVGPXVDQYIDP-UHFFFAOYSA-N borane Chemical class B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 description 3
- 150000001638 boron Chemical class 0.000 description 3
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 3
- 229940095259 butylated hydroxytoluene Drugs 0.000 description 3
- 150000001735 carboxylic acids Chemical class 0.000 description 3
- 239000012876 carrier material Substances 0.000 description 3
- 150000001787 chalcogens Chemical class 0.000 description 3
- 229910052804 chromium Inorganic materials 0.000 description 3
- 239000011651 chromium Substances 0.000 description 3
- 239000003431 cross linking reagent Substances 0.000 description 3
- RAABOESOVLLHRU-UHFFFAOYSA-N diazene Chemical compound N=N RAABOESOVLLHRU-UHFFFAOYSA-N 0.000 description 3
- 125000005678 ethenylene group Chemical group [H]C([*:1])=C([H])[*:2] 0.000 description 3
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 3
- 150000002170 ethers Chemical class 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 229920000578 graft copolymer Polymers 0.000 description 3
- 229920006270 hydrocarbon resin Polymers 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- 150000003949 imides Chemical class 0.000 description 3
- 230000001976 improved effect Effects 0.000 description 3
- 238000011065 in-situ storage Methods 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- 229910052809 inorganic oxide Inorganic materials 0.000 description 3
- 238000003780 insertion Methods 0.000 description 3
- 230000037431 insertion Effects 0.000 description 3
- 229920001580 isotactic polymer Polymers 0.000 description 3
- 229910052744 lithium Inorganic materials 0.000 description 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical group OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 3
- 239000011976 maleic acid Chemical group 0.000 description 3
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical group O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 239000002808 molecular sieve Substances 0.000 description 3
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 3
- FTQWRYSLUYAIRQ-UHFFFAOYSA-N n-[(octadecanoylamino)methyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCNC(=O)CCCCCCCCCCCCCCCCC FTQWRYSLUYAIRQ-UHFFFAOYSA-N 0.000 description 3
- 125000006574 non-aromatic ring group Chemical group 0.000 description 3
- 239000004745 nonwoven fabric Substances 0.000 description 3
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 3
- 150000003063 pnictogens Chemical class 0.000 description 3
- 229920005629 polypropylene homopolymer Polymers 0.000 description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 229910052814 silicon oxide Inorganic materials 0.000 description 3
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 3
- 238000001228 spectrum Methods 0.000 description 3
- 229920001169 thermoplastic Polymers 0.000 description 3
- ORYGRKHDLWYTKX-UHFFFAOYSA-N trihexylalumane Chemical compound CCCCCC[Al](CCCCCC)CCCCCC ORYGRKHDLWYTKX-UHFFFAOYSA-N 0.000 description 3
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 3
- 239000002023 wood Substances 0.000 description 3
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 description 2
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical compound C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 description 2
- MFWFDRBPQDXFRC-LNTINUHCSA-N (z)-4-hydroxypent-3-en-2-one;vanadium Chemical compound [V].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O MFWFDRBPQDXFRC-LNTINUHCSA-N 0.000 description 2
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- QWUWMCYKGHVNAV-UHFFFAOYSA-N 1,2-dihydrostilbene Chemical group C=1C=CC=CC=1CCC1=CC=CC=C1 QWUWMCYKGHVNAV-UHFFFAOYSA-N 0.000 description 2
- LEFWFSPJGPJWLC-UHFFFAOYSA-L 1-adamantylazanide titanium(3+) dichloride Chemical compound [Cl-].[Cl-].[Ti+3].C12(CC3CC(CC(C1)C3)C2)[NH-] LEFWFSPJGPJWLC-UHFFFAOYSA-L 0.000 description 2
- LRTOHSLOFCWHRF-UHFFFAOYSA-N 1-methyl-1h-indene Chemical compound C1=CC=C2C(C)C=CC2=C1 LRTOHSLOFCWHRF-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- ASGNRCDZSRNHOP-UHFFFAOYSA-N 2-methyl-4-phenyl-1h-indene Chemical compound C1C(C)=CC2=C1C=CC=C2C1=CC=CC=C1 ASGNRCDZSRNHOP-UHFFFAOYSA-N 0.000 description 2
- MHNNAWXXUZQSNM-UHFFFAOYSA-N 2-methylbut-1-ene Chemical compound CCC(C)=C MHNNAWXXUZQSNM-UHFFFAOYSA-N 0.000 description 2
- 125000004975 3-butenyl group Chemical group C(CC=C)* 0.000 description 2
- 229910018516 Al—O Inorganic materials 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- JSFCROZLEHMLRW-UHFFFAOYSA-N CC(C(C1=CC=C2)[Zr](C)(C3C4=CC=CC(C5=CC=CC=C5)=C4C=C3C)[SiH2]C3=CC=CC=C3)=CC1=C2C1=CC=CC=C1.Cl.Cl Chemical compound CC(C(C1=CC=C2)[Zr](C)(C3C4=CC=CC(C5=CC=CC=C5)=C4C=C3C)[SiH2]C3=CC=CC=C3)=CC1=C2C1=CC=CC=C1.Cl.Cl JSFCROZLEHMLRW-UHFFFAOYSA-N 0.000 description 2
- BOOHTEYYVQAWMD-UHFFFAOYSA-N CC1=CC2=CC=CC=C2C1[Hf](C)(C1C2=CC=CC=C2C=C1C)[SiH2]C1=CC=CC=C1.Cl.Cl Chemical compound CC1=CC2=CC=CC=C2C1[Hf](C)(C1C2=CC=CC=C2C=C1C)[SiH2]C1=CC=CC=C1.Cl.Cl BOOHTEYYVQAWMD-UHFFFAOYSA-N 0.000 description 2
- PCEUKHDUMPARIN-UHFFFAOYSA-N CC1=CC2=CC=CC=C2C1[Zr](C)(C1C2=CC=CC=C2C=C1C)[SiH2]C1=CC=CC=C1.Cl.Cl Chemical compound CC1=CC2=CC=CC=C2C1[Zr](C)(C1C2=CC=CC=C2C=C1C)[SiH2]C1=CC=CC=C1.Cl.Cl PCEUKHDUMPARIN-UHFFFAOYSA-N 0.000 description 2
- PHPWWQLIZHPMHX-UHFFFAOYSA-N CN(C)C1=CC=CC=C1.CN(C)C1=CC=CC=C1.CN(C)C1=CC=CC=C1.OB(O)O.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F Chemical compound CN(C)C1=CC=CC=C1.CN(C)C1=CC=CC=C1.CN(C)C1=CC=CC=C1.OB(O)O.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F PHPWWQLIZHPMHX-UHFFFAOYSA-N 0.000 description 2
- FEMGAXGLTIYWRE-UHFFFAOYSA-N C[Zr](C1C2=CC=CCC2CC1)(C1C2=CC=CCC2CC1)[SiH2]C1=CC=CC=C1.Cl.Cl Chemical compound C[Zr](C1C2=CC=CCC2CC1)(C1C2=CC=CCC2CC1)[SiH2]C1=CC=CC=C1.Cl.Cl FEMGAXGLTIYWRE-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-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
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 2
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methylaniline Chemical compound CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical class OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- FOIXSVOLVBLSDH-UHFFFAOYSA-N Silver ion Chemical compound [Ag+] FOIXSVOLVBLSDH-UHFFFAOYSA-N 0.000 description 2
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 2
- 239000004809 Teflon Substances 0.000 description 2
- 229920006362 Teflon® Polymers 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- YHYHCGCMYMMXAH-UHFFFAOYSA-L [Cl-].[Cl-].C1(=CC=CC=C1)[SiH](C1=CC=CC=C1)[Zr+2](C1CCC2CC=CC=C12)C1CCC2CC=CC=C12 Chemical compound [Cl-].[Cl-].C1(=CC=CC=C1)[SiH](C1=CC=CC=C1)[Zr+2](C1CCC2CC=CC=C12)C1CCC2CC=CC=C12 YHYHCGCMYMMXAH-UHFFFAOYSA-L 0.000 description 2
- GVMCJEXOZRLPKR-UHFFFAOYSA-L [Cl-].[Cl-].C1(CCC2CC=CC=C12)[Hf+2]C1CCC2CC=CC=C12.C=C Chemical compound [Cl-].[Cl-].C1(CCC2CC=CC=C12)[Hf+2]C1CCC2CC=CC=C12.C=C GVMCJEXOZRLPKR-UHFFFAOYSA-L 0.000 description 2
- NFNBXPIIOMPJQE-UHFFFAOYSA-L [Cl-].[Cl-].C1=CC(C(=CC=C2C)C)=C2C1[Hf+2](=C)C1C(C(C)=CC=C2C)=C2C=C1 Chemical compound [Cl-].[Cl-].C1=CC(C(=CC=C2C)C)=C2C1[Hf+2](=C)C1C(C(C)=CC=C2C)=C2C=C1 NFNBXPIIOMPJQE-UHFFFAOYSA-L 0.000 description 2
- KNRYBQYJVYZOQB-UHFFFAOYSA-L [Cl-].[Cl-].C1=CC(C(=CC=C2C)C)=C2C1[Zr+2](=C)C1C(C(C)=CC=C2C)=C2C=C1 Chemical compound [Cl-].[Cl-].C1=CC(C(=CC=C2C)C)=C2C1[Zr+2](=C)C1C(C(C)=CC=C2C)=C2C=C1 KNRYBQYJVYZOQB-UHFFFAOYSA-L 0.000 description 2
- IGSPQDBOJOXEJJ-UHFFFAOYSA-L [Cl-].[Cl-].C1=CC2=CC=CC=C2C1[Hf+2](=C)C1C2=CC=CC=C2C=C1 Chemical compound [Cl-].[Cl-].C1=CC2=CC=CC=C2C1[Hf+2](=C)C1C2=CC=CC=C2C=C1 IGSPQDBOJOXEJJ-UHFFFAOYSA-L 0.000 description 2
- ZUGAYUSVYHLKDE-UHFFFAOYSA-L [Cl-].[Cl-].C1=CC2=CC=CC=C2C1[Zr+2](=C)C1C2=CC=CC=C2C=C1 Chemical compound [Cl-].[Cl-].C1=CC2=CC=CC=C2C1[Zr+2](=C)C1C2=CC=CC=C2C=C1 ZUGAYUSVYHLKDE-UHFFFAOYSA-L 0.000 description 2
- IPFOHNSBHKSSCX-UHFFFAOYSA-L [Cl-].[Cl-].C1CC2CC=CC=C2C1[Hf+2](=C)C1C2=CC=CCC2CC1 Chemical compound [Cl-].[Cl-].C1CC2CC=CC=C2C1[Hf+2](=C)C1C2=CC=CCC2CC1 IPFOHNSBHKSSCX-UHFFFAOYSA-L 0.000 description 2
- QHHXDHRTYCUORU-UHFFFAOYSA-L [Cl-].[Cl-].C1CC2CC=CC=C2C1[Zr+2](=C)C1C2=CC=CCC2CC1 Chemical compound [Cl-].[Cl-].C1CC2CC=CC=C2C1[Zr+2](=C)C1C2=CC=CCC2CC1 QHHXDHRTYCUORU-UHFFFAOYSA-L 0.000 description 2
- NDJMNNSJDIFFTH-UHFFFAOYSA-L [Cl-].[Cl-].CC1=CC(C(=CC=C2)C=3C=CC=CC=3)=C2C1[Zr+2]([SiH](C)C)C1C(C)=CC2=C1C=CC=C2C1=CC=CC=C1 Chemical compound [Cl-].[Cl-].CC1=CC(C(=CC=C2)C=3C=CC=CC=3)=C2C1[Zr+2]([SiH](C)C)C1C(C)=CC2=C1C=CC=C2C1=CC=CC=C1 NDJMNNSJDIFFTH-UHFFFAOYSA-L 0.000 description 2
- MOMFNNODEDMKRW-UHFFFAOYSA-L [Cl-].[Cl-].CC1=CC2=CC=CC=C2C1[Zr+2](=C)C1C2=CC=CC=C2C=C1C Chemical compound [Cl-].[Cl-].CC1=CC2=CC=CC=C2C1[Zr+2](=C)C1C2=CC=CC=C2C=C1C MOMFNNODEDMKRW-UHFFFAOYSA-L 0.000 description 2
- IVZHJEOMGNUPTC-UHFFFAOYSA-L [Cl-].[Cl-].CC1=Cc2c(cccc2-c2ccccc2)C1[Hf++](=C)C1C(C)=Cc2c1cccc2-c1ccccc1 Chemical compound [Cl-].[Cl-].CC1=Cc2c(cccc2-c2ccccc2)C1[Hf++](=C)C1C(C)=Cc2c1cccc2-c1ccccc1 IVZHJEOMGNUPTC-UHFFFAOYSA-L 0.000 description 2
- KLOBHLFYIOQEOF-UHFFFAOYSA-L [Cl-].[Cl-].CC1=Cc2c(cccc2-c2ccccc2)C1[Hf++](C1C(C)=Cc2c1cccc2-c1ccccc1)[SiH](c1ccccc1)c1ccccc1 Chemical compound [Cl-].[Cl-].CC1=Cc2c(cccc2-c2ccccc2)C1[Hf++](C1C(C)=Cc2c1cccc2-c1ccccc1)[SiH](c1ccccc1)c1ccccc1 KLOBHLFYIOQEOF-UHFFFAOYSA-L 0.000 description 2
- WKWATPQNSRSHDL-UHFFFAOYSA-L [Cl-].[Cl-].CC1=Cc2ccccc2C1[Hf++](=C)C1C(C)=Cc2ccccc12 Chemical compound [Cl-].[Cl-].CC1=Cc2ccccc2C1[Hf++](=C)C1C(C)=Cc2ccccc12 WKWATPQNSRSHDL-UHFFFAOYSA-L 0.000 description 2
- ONIXKSAHVIIWFQ-UHFFFAOYSA-L [Cl-].[Cl-].C[SiH](C)[Zr++](C1C=Cc2c1c(C)ccc2C)C1C=Cc2c1c(C)ccc2C Chemical compound [Cl-].[Cl-].C[SiH](C)[Zr++](C1C=Cc2c1c(C)ccc2C)C1C=Cc2c1c(C)ccc2C ONIXKSAHVIIWFQ-UHFFFAOYSA-L 0.000 description 2
- TYGPYZGVLXKYCG-UHFFFAOYSA-L [Cl-].[Cl-].Cc1ccc(C)c2C(C=Cc12)[Hf++](C1C=Cc2c1c(C)ccc2C)[SiH](c1ccccc1)c1ccccc1 Chemical compound [Cl-].[Cl-].Cc1ccc(C)c2C(C=Cc12)[Hf++](C1C=Cc2c1c(C)ccc2C)[SiH](c1ccccc1)c1ccccc1 TYGPYZGVLXKYCG-UHFFFAOYSA-L 0.000 description 2
- CUJRVFIICFDLGR-UHFFFAOYSA-N acetylacetonate Chemical compound CC(=O)[CH-]C(C)=O CUJRVFIICFDLGR-UHFFFAOYSA-N 0.000 description 2
- 239000002318 adhesion promoter Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229920006271 aliphatic hydrocarbon resin Polymers 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N argon Substances [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 150000001491 aromatic compounds Chemical class 0.000 description 2
- 238000000889 atomisation Methods 0.000 description 2
- CUFNKYGDVFVPHO-UHFFFAOYSA-N azulene Chemical compound C1=CC=CC2=CC=CC2=C1 CUFNKYGDVFVPHO-UHFFFAOYSA-N 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 2
- LGBAGUMSAPUZPU-UHFFFAOYSA-N bis(9-methyldecyl) benzene-1,2-dicarboxylate Chemical compound CC(C)CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCC(C)C LGBAGUMSAPUZPU-UHFFFAOYSA-N 0.000 description 2
- 229920001400 block copolymer Polymers 0.000 description 2
- 229910000085 borane Inorganic materials 0.000 description 2
- 150000001639 boron compounds Chemical class 0.000 description 2
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 2
- UJYLYGDHTIVYRI-UHFFFAOYSA-N cadmium(2+);ethane Chemical compound [Cd+2].[CH2-]C.[CH2-]C UJYLYGDHTIVYRI-UHFFFAOYSA-N 0.000 description 2
- 238000004364 calculation method Methods 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
- 239000011111 cardboard Substances 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 239000003426 co-catalyst Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 150000001923 cyclic compounds Chemical class 0.000 description 2
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 description 2
- 239000000539 dimer Substances 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- UGJSEFCFZLUFIN-UHFFFAOYSA-N diphenylmethylbenzene 1,2,3,4,5-pentafluoro-6-(2,3,4,5,6-pentafluorophenyl)benzene borate Chemical compound [O-]B([O-])[O-].c1ccc(cc1)[C+](c1ccccc1)c1ccccc1.c1ccc(cc1)[C+](c1ccccc1)c1ccccc1.c1ccc(cc1)[C+](c1ccccc1)c1ccccc1.Fc1c(F)c(F)c(c(F)c1F)-c1c(F)c(F)c(F)c(F)c1F.Fc1c(F)c(F)c(c(F)c1F)-c1c(F)c(F)c(F)c(F)c1F.Fc1c(F)c(F)c(c(F)c1F)-c1c(F)c(F)c(F)c(F)c1F.Fc1c(F)c(F)c(c(F)c1F)-c1c(F)c(F)c(F)c(F)c1F UGJSEFCFZLUFIN-UHFFFAOYSA-N 0.000 description 2
- IYPLTVKTLDQUGG-UHFFFAOYSA-N dodeca-1,11-diene Chemical compound C=CCCCCCCCCC=C IYPLTVKTLDQUGG-UHFFFAOYSA-N 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 229920001038 ethylene copolymer Polymers 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 230000009969 flowable effect Effects 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 229910052733 gallium Inorganic materials 0.000 description 2
- 238000012685 gas phase polymerization Methods 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- GEAWFZNTIFJMHR-UHFFFAOYSA-N hepta-1,6-diene Chemical compound C=CCCCC=C GEAWFZNTIFJMHR-UHFFFAOYSA-N 0.000 description 2
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 230000010354 integration Effects 0.000 description 2
- 150000008040 ionic compounds Chemical group 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 2
- 239000002655 kraft paper Substances 0.000 description 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 239000012685 metal catalyst precursor Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- CYQYCASVINMDFD-UHFFFAOYSA-N n,n-ditert-butyl-2-methylpropan-2-amine Chemical compound CC(C)(C)N(C(C)(C)C)C(C)(C)C CYQYCASVINMDFD-UHFFFAOYSA-N 0.000 description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- SJYNFBVQFBRSIB-UHFFFAOYSA-N norbornadiene Chemical compound C1=CC2C=CC1C2 SJYNFBVQFBRSIB-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
- 230000000269 nucleophilic effect Effects 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-M phenolate Chemical compound [O-]C1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-M 0.000 description 2
- 229930015698 phenylpropene Natural products 0.000 description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 2
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 2
- 239000006069 physical mixture Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 150000003097 polyterpenes Chemical class 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000011045 prefiltration Methods 0.000 description 2
- 229920001384 propylene homopolymer Polymers 0.000 description 2
- 238000010926 purge Methods 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 229940054334 silver cation Drugs 0.000 description 2
- SCABQASLNUQUKD-UHFFFAOYSA-N silylium Chemical compound [SiH3+] SCABQASLNUQUKD-UHFFFAOYSA-N 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 239000003784 tall oil Substances 0.000 description 2
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 2
- 229920002725 thermoplastic elastomer Polymers 0.000 description 2
- 239000004416 thermosoftening plastic Substances 0.000 description 2
- 239000011135 tin Substances 0.000 description 2
- 229910052718 tin Inorganic materials 0.000 description 2
- 239000004408 titanium dioxide Substances 0.000 description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 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
- OBAJXDYVZBHCGT-UHFFFAOYSA-N tris(pentafluorophenyl)borane Chemical compound FC1=C(F)C(F)=C(F)C(F)=C1B(C=1C(=C(F)C(F)=C(F)C=1F)F)C1=C(F)C(F)=C(F)C(F)=C1F OBAJXDYVZBHCGT-UHFFFAOYSA-N 0.000 description 2
- 238000004260 weight control Methods 0.000 description 2
- 239000010457 zeolite Substances 0.000 description 2
- HEPBQSXQJMTVFI-UHFFFAOYSA-N zinc;butane Chemical compound [Zn+2].CCC[CH2-].CCC[CH2-] HEPBQSXQJMTVFI-UHFFFAOYSA-N 0.000 description 2
- LLWKIYGBECGCKZ-FNORWQNLSA-N (3E)-docosa-1,3-diene Chemical compound CCCCCCCCCCCCCCCCCC\C=C\C=C LLWKIYGBECGCKZ-FNORWQNLSA-N 0.000 description 1
- JDQDKSFVTRSLMA-FNORWQNLSA-N (3E)-hexacosa-1,3-diene Chemical compound CCCCCCCCCCCCCCCCCCCCCC\C=C\C=C JDQDKSFVTRSLMA-FNORWQNLSA-N 0.000 description 1
- OGBLSRZNQXYNEF-FNORWQNLSA-N (3E)-octacosa-1,3-diene Chemical compound CCCCCCCCCCCCCCCCCCCCCCCC\C=C\C=C OGBLSRZNQXYNEF-FNORWQNLSA-N 0.000 description 1
- YKTJTYUXGJIHKT-FNORWQNLSA-N (3E)-pentacosa-1,3-diene Chemical compound CCCCCCCCCCCCCCCCCCCCC\C=C\C=C YKTJTYUXGJIHKT-FNORWQNLSA-N 0.000 description 1
- HRZMCADYEQRDQZ-FNORWQNLSA-N (3E)-tetracosa-1,3-diene Chemical compound CCCCCCCCCCCCCCCCCCCC\C=C\C=C HRZMCADYEQRDQZ-FNORWQNLSA-N 0.000 description 1
- MPTCWBZQGJMVAJ-FNORWQNLSA-N (3E)-triaconta-1,3-diene Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCC\C=C\C=C MPTCWBZQGJMVAJ-FNORWQNLSA-N 0.000 description 1
- VSDCOAJFNDHAFC-FNORWQNLSA-N (3E)-tricosa-1,3-diene Chemical compound CCCCCCCCCCCCCCCCCCC\C=C\C=C VSDCOAJFNDHAFC-FNORWQNLSA-N 0.000 description 1
- YHHHHJCAVQSFMJ-FNORWQNLSA-N (3e)-deca-1,3-diene Chemical compound CCCCCC\C=C\C=C YHHHHJCAVQSFMJ-FNORWQNLSA-N 0.000 description 1
- VUIFFVOKIWOJBA-FNORWQNLSA-N (3e)-dodeca-1,3-diene Chemical compound CCCCCCCC\C=C\C=C VUIFFVOKIWOJBA-FNORWQNLSA-N 0.000 description 1
- OGQVROWWFUXRST-FNORWQNLSA-N (3e)-hepta-1,3-diene Chemical compound CCC\C=C\C=C OGQVROWWFUXRST-FNORWQNLSA-N 0.000 description 1
- PEUHBSAKNWEJHZ-FNORWQNLSA-N (3e)-heptadeca-1,3-diene Chemical compound CCCCCCCCCCCCC\C=C\C=C PEUHBSAKNWEJHZ-FNORWQNLSA-N 0.000 description 1
- FNJOJJWNIKUCMT-FNORWQNLSA-N (3e)-hexadeca-1,3-diene Chemical compound CCCCCCCCCCCC\C=C\C=C FNJOJJWNIKUCMT-FNORWQNLSA-N 0.000 description 1
- CLNYHERYALISIR-FNORWQNLSA-N (3e)-nona-1,3-diene Chemical compound CCCCC\C=C\C=C CLNYHERYALISIR-FNORWQNLSA-N 0.000 description 1
- WHUHTCSYMDOIGU-FNORWQNLSA-N (3e)-octadeca-1,3-diene Chemical compound CCCCCCCCCCCCCC\C=C\C=C WHUHTCSYMDOIGU-FNORWQNLSA-N 0.000 description 1
- SHWRGPMBBKBLKB-FNORWQNLSA-N (3e)-pentadeca-1,3-diene Chemical compound CCCCCCCCCCC\C=C\C=C SHWRGPMBBKBLKB-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
- IRVGWDJFZXOKDK-FNORWQNLSA-N (3e)-trideca-1,3-diene Chemical compound CCCCCCCCC\C=C\C=C IRVGWDJFZXOKDK-FNORWQNLSA-N 0.000 description 1
- RSLLXTJELTWVHR-FNORWQNLSA-N (3e)-undeca-1,3-diene Chemical compound CCCCCCC\C=C\C=C RSLLXTJELTWVHR-FNORWQNLSA-N 0.000 description 1
- CHEANNSDVJOIBS-MHZLTWQESA-N (3s)-3-cyclopropyl-3-[3-[[3-(5,5-dimethylcyclopenten-1-yl)-4-(2-fluoro-5-methoxyphenyl)phenyl]methoxy]phenyl]propanoic acid Chemical compound COC1=CC=C(F)C(C=2C(=CC(COC=3C=C(C=CC=3)[C@@H](CC(O)=O)C3CC3)=CC=2)C=2C(CCC=2)(C)C)=C1 CHEANNSDVJOIBS-MHZLTWQESA-N 0.000 description 1
- KWUWRILZYFCPRI-ADYYPQGGSA-N (7Z,11Z)-nonacosa-7,11-diene Chemical compound CCCCCCCCCCCCCCCCC\C=C/CC\C=C/CCCCCC KWUWRILZYFCPRI-ADYYPQGGSA-N 0.000 description 1
- FSJSYDFBTIVUFD-SUKNRPLKSA-N (z)-4-hydroxypent-3-en-2-one;oxovanadium Chemical compound [V]=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O FSJSYDFBTIVUFD-SUKNRPLKSA-N 0.000 description 1
- POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 description 1
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
- VOSLXTGMYNYCPW-UHFFFAOYSA-N 1,10-Undecadiene Chemical compound C=CCCCCCCCC=C VOSLXTGMYNYCPW-UHFFFAOYSA-N 0.000 description 1
- BPHFKBMQSYYNGQ-UHFFFAOYSA-N 1,12-Tridecadiene Chemical compound C=CCCCCCCCCCC=C BPHFKBMQSYYNGQ-UHFFFAOYSA-N 0.000 description 1
- QTYUSOHYEPOHLV-FNORWQNLSA-N 1,3-Octadiene Chemical compound CCCC\C=C\C=C QTYUSOHYEPOHLV-FNORWQNLSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- PRBHEGAFLDMLAL-UHFFFAOYSA-N 1,5-Hexadiene Natural products CC=CCC=C PRBHEGAFLDMLAL-UHFFFAOYSA-N 0.000 description 1
- YBCVSZCMASDRCS-UHFFFAOYSA-N 1-[ethoxy-[ethoxy-(2-methoxyphenoxy)-propoxymethyl]sulfanyl-propoxymethoxy]-2-methoxybenzene Chemical compound C=1C=CC=C(OC)C=1OC(OCC)(OCCC)SC(OCC)(OCCC)OC1=CC=CC=C1OC YBCVSZCMASDRCS-UHFFFAOYSA-N 0.000 description 1
- 125000004973 1-butenyl group Chemical group C(=CCC)* 0.000 description 1
- HYOHWHHFTYGMJS-UHFFFAOYSA-N 1-ethenyladamantane Chemical compound C1C(C2)CC3CC2CC1(C=C)C3 HYOHWHHFTYGMJS-UHFFFAOYSA-N 0.000 description 1
- SDRZFSPCVYEJTP-UHFFFAOYSA-N 1-ethenylcyclohexene Chemical compound C=CC1=CCCCC1 SDRZFSPCVYEJTP-UHFFFAOYSA-N 0.000 description 1
- 125000006019 1-methyl-1-propenyl group Chemical group 0.000 description 1
- 125000006021 1-methyl-2-propenyl group Chemical group 0.000 description 1
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 description 1
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 1
- CORHDXNAYKUXRI-UHFFFAOYSA-N 1h-cyclopenta[12]annulene Chemical compound C1=CC=CC=CC=CC=CC2=C1CC=C2 CORHDXNAYKUXRI-UHFFFAOYSA-N 0.000 description 1
- OJKKCHGJEXMEDM-UHFFFAOYSA-N 2,5,5-trichlorocyclohexa-1,3-diene Chemical compound ClC1=CCC(Cl)(Cl)C=C1 OJKKCHGJEXMEDM-UHFFFAOYSA-N 0.000 description 1
- NMXLXQGHBSPIDR-UHFFFAOYSA-N 2-(2-methylpropyl)oxaluminane Chemical compound CC(C)C[Al]1CCCCO1 NMXLXQGHBSPIDR-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- 125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 1
- YVSMQHYREUQGRX-UHFFFAOYSA-N 2-ethyloxaluminane Chemical compound CC[Al]1CCCCO1 YVSMQHYREUQGRX-UHFFFAOYSA-N 0.000 description 1
- NJYTVNWDHPUNTD-UHFFFAOYSA-N 2-methyl-1-[(2-methyl-4-phenyl-1h-inden-1-yl)methyl]-4-phenyl-1h-indene Chemical compound CC1=CC(C(=CC=C2)C=3C=CC=CC=3)=C2C1CC1C(C)=CC2=C1C=CC=C2C1=CC=CC=C1 NJYTVNWDHPUNTD-UHFFFAOYSA-N 0.000 description 1
- XANDUUDKRPWWBO-UHFFFAOYSA-N 2-methyl-1-[2-(2-methyl-1h-inden-1-yl)ethyl]-1h-indene Chemical compound CC1=CC2=CC=CC=C2C1CCC1C2=CC=CC=C2C=C1C XANDUUDKRPWWBO-UHFFFAOYSA-N 0.000 description 1
- 125000006020 2-methyl-1-propenyl group Chemical group 0.000 description 1
- YSAXEHWHSLANOM-UHFFFAOYSA-N 2-methyl-1h-indene Chemical compound C1=CC=C2CC(C)=CC2=C1 YSAXEHWHSLANOM-UHFFFAOYSA-N 0.000 description 1
- 125000004493 2-methylbut-1-yl group Chemical group CC(C*)CC 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- DKLQZDIAQKGVTA-UHFFFAOYSA-N 4,7-dimethyl-1h-indene Chemical compound CC1=CC=C(C)C2=C1CC=C2 DKLQZDIAQKGVTA-UHFFFAOYSA-N 0.000 description 1
- JLBJTVDPSNHSKJ-UHFFFAOYSA-N 4-Methylstyrene Chemical compound CC1=CC=C(C=C)C=C1 JLBJTVDPSNHSKJ-UHFFFAOYSA-N 0.000 description 1
- XYZWMVYYUIMRIZ-UHFFFAOYSA-N 4-bromo-n,n-dimethylaniline Chemical compound CN(C)C1=CC=C(Br)C=C1 XYZWMVYYUIMRIZ-UHFFFAOYSA-N 0.000 description 1
- FERQWJMFSVKKGT-UHFFFAOYSA-N 5-ethylnon-1-ene Chemical compound CCCCC(CC)CCC=C FERQWJMFSVKKGT-UHFFFAOYSA-N 0.000 description 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 1
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical group CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 1
- UIERETOOQGIECD-UHFFFAOYSA-N Angelic acid Natural products CC=C(C)C(O)=O UIERETOOQGIECD-UHFFFAOYSA-N 0.000 description 1
- 229910000897 Babbitt (metal) Inorganic materials 0.000 description 1
- IPGRRJHICAYLLL-UHFFFAOYSA-N C1(=CC=CC=C1)C(C1=CC=CC=C1)=CC(C)(C)C=1C=CC=C2C=3C=C(C=C(C3CC12)C1C=CC=C1)C(C)(C)C Chemical compound C1(=CC=CC=C1)C(C1=CC=CC=C1)=CC(C)(C)C=1C=CC=C2C=3C=C(C=C(C3CC12)C1C=CC=C1)C(C)(C)C IPGRRJHICAYLLL-UHFFFAOYSA-N 0.000 description 1
- ZXXQLPKWALCVTA-UHFFFAOYSA-N C1=CC([Si](CC)(CC)CC)=CC=C1C(C=1C=CC(=CC=1)[Si](CC)(CC)CC)=C1C=CC=C1 Chemical compound C1=CC([Si](CC)(CC)CC)=CC=C1C(C=1C=CC(=CC=1)[Si](CC)(CC)CC)=C1C=CC=C1 ZXXQLPKWALCVTA-UHFFFAOYSA-N 0.000 description 1
- AIIMWBOOVDEVAR-UHFFFAOYSA-N C1=CC2=CC=CC=C2C1[Zr]([SiH](C)C)C1C2=CC=CC=C2C=C1 Chemical compound C1=CC2=CC=CC=C2C1[Zr]([SiH](C)C)C1C2=CC=CC=C2C=C1 AIIMWBOOVDEVAR-UHFFFAOYSA-N 0.000 description 1
- MWZISNRLKLPKMO-UHFFFAOYSA-L C1=CC=C2C(C3=CC=CC4=C3C=C(C)C4[Zr](Cl)(Cl)(=C)C3C4=C(C(=CC=C4)C=4C5=CC=CC=C5C=CC=4)C=C3C)=CC=CC2=C1 Chemical compound C1=CC=C2C(C3=CC=CC4=C3C=C(C)C4[Zr](Cl)(Cl)(=C)C3C4=C(C(=CC=C4)C=4C5=CC=CC=C5C=CC=4)C=C3C)=CC=CC2=C1 MWZISNRLKLPKMO-UHFFFAOYSA-L 0.000 description 1
- HCDYOWWRPRWLBK-UHFFFAOYSA-L C1=CC=C2C(C3=CC=CC4=C3C=C(C)C4[Zr](Cl)(Cl)(C3C4=C(C(=CC=C4)C=4C5=CC=CC=C5C=CC=4)C=C3C)[SiH](C)C)=CC=CC2=C1 Chemical compound C1=CC=C2C(C3=CC=CC4=C3C=C(C)C4[Zr](Cl)(Cl)(C3C4=C(C(=CC=C4)C=4C5=CC=CC=C5C=CC=4)C=C3C)[SiH](C)C)=CC=CC2=C1 HCDYOWWRPRWLBK-UHFFFAOYSA-L 0.000 description 1
- NTQWAWROVHMHBQ-UHFFFAOYSA-N C1CC2(CC1C1=CCC=C21)[Zr]C12CCC(C1)C1=CCC=C21 Chemical compound C1CC2(CC1C1=CCC=C21)[Zr]C12CCC(C1)C1=CCC=C21 NTQWAWROVHMHBQ-UHFFFAOYSA-N 0.000 description 1
- OITLQHFSFQHOLH-UHFFFAOYSA-N CC(C(C1=CC=C2)[Hf](C)(C3C4=CC=CC(C5=CC=CC6=CC=CC=C56)=C4C=C3C)[SiH2]C3=CC=CC=C3)=CC1=C2C1=CC=CC2=CC=CC=C12.Cl.Cl Chemical compound CC(C(C1=CC=C2)[Hf](C)(C3C4=CC=CC(C5=CC=CC6=CC=CC=C56)=C4C=C3C)[SiH2]C3=CC=CC=C3)=CC1=C2C1=CC=CC2=CC=CC=C12.Cl.Cl OITLQHFSFQHOLH-UHFFFAOYSA-N 0.000 description 1
- QEEPLEFBPYDQON-UHFFFAOYSA-N CC(C(C1=CC=C2)[Zr](C)(C3C4=CC=CC(C5=CC=CC6=CC=CC=C56)=C4C=C3C)[SiH2]C3=CC=CC=C3)=CC1=C2C1=CC=CC2=CC=CC=C12.Cl.Cl Chemical compound CC(C(C1=CC=C2)[Zr](C)(C3C4=CC=CC(C5=CC=CC6=CC=CC=C56)=C4C=C3C)[SiH2]C3=CC=CC=C3)=CC1=C2C1=CC=CC2=CC=CC=C12.Cl.Cl QEEPLEFBPYDQON-UHFFFAOYSA-N 0.000 description 1
- FUMGNZDNNNPLHP-UHFFFAOYSA-N CC(C)(C)C1=CC(C2=CC=CC(C(C)(C)C)=C2C2)=C2C([Hf](C)(C2C=CC=C2)[SiH2]C2=CC=CC=C2)=C1.Cl.Cl Chemical compound CC(C)(C)C1=CC(C2=CC=CC(C(C)(C)C)=C2C2)=C2C([Hf](C)(C2C=CC=C2)[SiH2]C2=CC=CC=C2)=C1.Cl.Cl FUMGNZDNNNPLHP-UHFFFAOYSA-N 0.000 description 1
- RGYCLBPIHMQQFN-UHFFFAOYSA-N CC(C)(C)N(C(C)(C)C)C(C)(C)C.CC(C)(C)N(C(C)(C)C)C(C)(C)C.CC(C)(C)N(C(C)(C)C)C(C)(C)C.OB(O)O.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F Chemical compound CC(C)(C)N(C(C)(C)C)C(C)(C)C.CC(C)(C)N(C(C)(C)C)C(C)(C)C.CC(C)(C)N(C(C)(C)C)C(C)(C)C.OB(O)O.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F RGYCLBPIHMQQFN-UHFFFAOYSA-N 0.000 description 1
- KNGQEWZNQLLQPZ-UHFFFAOYSA-L CC(C)=[Hf](Cl)(Cl)(C1C=CC=C1)C1=CC=CC2=C1CC1=CC=CC=C21 Chemical compound CC(C)=[Hf](Cl)(Cl)(C1C=CC=C1)C1=CC=CC2=C1CC1=CC=CC=C21 KNGQEWZNQLLQPZ-UHFFFAOYSA-L 0.000 description 1
- XJTQEAXBIXXILJ-UHFFFAOYSA-L CC(C)=[Zr](Cl)(Cl)(C1C=CC=C1)C1=CC=CC2=C1CC1=CC=CC=C21 Chemical compound CC(C)=[Zr](Cl)(Cl)(C1C=CC=C1)C1=CC=CC2=C1CC1=CC=CC=C21 XJTQEAXBIXXILJ-UHFFFAOYSA-L 0.000 description 1
- VWEXVZUSTJZQMA-UHFFFAOYSA-N CC(C=C1C)=CC(C)=C1N(C)C.CC(C=C1C)=CC(C)=C1N(C)C.CC(C=C1C)=CC(C)=C1N(C)C.OB(O)O.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F Chemical compound CC(C=C1C)=CC(C)=C1N(C)C.CC(C=C1C)=CC(C)=C1N(C)C.CC(C=C1C)=CC(C)=C1N(C)C.OB(O)O.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F VWEXVZUSTJZQMA-UHFFFAOYSA-N 0.000 description 1
- WSCXFHUAMAAYAP-UHFFFAOYSA-L CC1=C(C)C(C=C1)[Hf](Cl)(Cl)(=C)C1C=CC(C)=C1C Chemical compound CC1=C(C)C(C=C1)[Hf](Cl)(Cl)(=C)C1C=CC(C)=C1C WSCXFHUAMAAYAP-UHFFFAOYSA-L 0.000 description 1
- CCRSBAPACFWDLW-UHFFFAOYSA-L CC1=C(C)C(C=C1)[Hf](Cl)(Cl)(C1C=CC(C)=C1C)[SiH](C1=CC=CC=C1)C1=CC=CC=C1 Chemical compound CC1=C(C)C(C=C1)[Hf](Cl)(Cl)(C1C=CC(C)=C1C)[SiH](C1=CC=CC=C1)C1=CC=CC=C1 CCRSBAPACFWDLW-UHFFFAOYSA-L 0.000 description 1
- CAWJOXPONCTULN-UHFFFAOYSA-L CC1=C(C)C(C=C1)[Zr](Cl)(Cl)(=C)C1C=CC(C)=C1C Chemical compound CC1=C(C)C(C=C1)[Zr](Cl)(Cl)(=C)C1C=CC(C)=C1C CAWJOXPONCTULN-UHFFFAOYSA-L 0.000 description 1
- MHJAPSRCDXSJHN-UHFFFAOYSA-N CC1=C(C)C=CC1[Hf](C)(C1C(C)=C(C)C=C1)[SiH2]C1=CC=CC=C1.Cl.Cl Chemical compound CC1=C(C)C=CC1[Hf](C)(C1C(C)=C(C)C=C1)[SiH2]C1=CC=CC=C1.Cl.Cl MHJAPSRCDXSJHN-UHFFFAOYSA-N 0.000 description 1
- DRJBONPCHLZUKH-UHFFFAOYSA-N CC1=C(C)C=CC1[Zr](C)(C1C(C)=C(C)C=C1)[SiH2]C1=CC=CC=C1.Cl Chemical compound CC1=C(C)C=CC1[Zr](C)(C1C(C)=C(C)C=C1)[SiH2]C1=CC=CC=C1.Cl DRJBONPCHLZUKH-UHFFFAOYSA-N 0.000 description 1
- JGLHDILSBOSJPM-UHFFFAOYSA-L CC1=CC(C(=CC=C2)C=3C4=CC=CC=C4C=CC=3)=C2C1[Zr](Cl)(Cl)(C1C2=C(C(=CC=C2)C=2C3=CC=CC=C3C=CC=2)C=C1C)[SiH](C=1C=CC=CC=1)C1=CC=CC=C1 Chemical compound CC1=CC(C(=CC=C2)C=3C4=CC=CC=C4C=CC=3)=C2C1[Zr](Cl)(Cl)(C1C2=C(C(=CC=C2)C=2C3=CC=CC=C3C=CC=2)C=C1C)[SiH](C=1C=CC=CC=1)C1=CC=CC=C1 JGLHDILSBOSJPM-UHFFFAOYSA-L 0.000 description 1
- KRSXFHCXOCZSDL-UHFFFAOYSA-L CC1=CC(C(=CC=C2)C=3C=CC=CC=3)=C2C1[Zr](Cl)(Cl)([SiH](C=1C=CC=CC=1)C=1C=CC=CC=1)C1C(C)=CC2=C1C=CC=C2C1=CC=CC=C1 Chemical compound CC1=CC(C(=CC=C2)C=3C=CC=CC=3)=C2C1[Zr](Cl)(Cl)([SiH](C=1C=CC=CC=1)C=1C=CC=CC=1)C1C(C)=CC2=C1C=CC=C2C1=CC=CC=C1 KRSXFHCXOCZSDL-UHFFFAOYSA-L 0.000 description 1
- QSBPXEDWBXHWKP-UHFFFAOYSA-N CC1=CC(C(=CC=C2)C=3C=CC=CC=3)=C2C1[Zr]([SiH](C)C)C1C(C)=CC2=C1C=CC=C2C1=CC=CC=C1 Chemical compound CC1=CC(C(=CC=C2)C=3C=CC=CC=3)=C2C1[Zr]([SiH](C)C)C1C(C)=CC2=C1C=CC=C2C1=CC=CC=C1 QSBPXEDWBXHWKP-UHFFFAOYSA-N 0.000 description 1
- GYZFAUWZGBCUNJ-UHFFFAOYSA-L CC1=Cc2c(cccc2-c2cccc3ccccc23)C1[Hf](Cl)(Cl)(C1C(C)=Cc2c1cccc2-c1cccc2ccccc12)[SiH](c1ccccc1)c1ccccc1 Chemical compound CC1=Cc2c(cccc2-c2cccc3ccccc23)C1[Hf](Cl)(Cl)(C1C(C)=Cc2c1cccc2-c1cccc2ccccc12)[SiH](c1ccccc1)c1ccccc1 GYZFAUWZGBCUNJ-UHFFFAOYSA-L 0.000 description 1
- JHWSPUBCXFCFJR-UHFFFAOYSA-N CCC1=CC=C(C1NC(C)(C)C[SiH](C)C)C Chemical compound CCC1=CC=C(C1NC(C)(C)C[SiH](C)C)C JHWSPUBCXFCFJR-UHFFFAOYSA-N 0.000 description 1
- BKBFSTAARDXBIR-UHFFFAOYSA-N CCCBCCC Chemical compound CCCBCCC BKBFSTAARDXBIR-UHFFFAOYSA-N 0.000 description 1
- MOYCHTVQJYAQJJ-UHFFFAOYSA-N CCCCCCCCCCCCCCCCCCN(C)CCCCCCCCCCCCCCCCCC.FC(C(B(C(C(F)=C(C(F)=C1F)F)=C1F)C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(B(C(C(F)=C(C(F)=C1F)F)=C1F)C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.C1=NC2=CC=CC=C2N1 Chemical compound CCCCCCCCCCCCCCCCCCN(C)CCCCCCCCCCCCCCCCCC.FC(C(B(C(C(F)=C(C(F)=C1F)F)=C1F)C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(B(C(C(F)=C(C(F)=C1F)F)=C1F)C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.C1=NC2=CC=CC=C2N1 MOYCHTVQJYAQJJ-UHFFFAOYSA-N 0.000 description 1
- DPOMYQPPWKUQEK-UHFFFAOYSA-N CCCCN(CCCC)CCCC.CCCCN(CCCC)CCCC.CCCCN(CCCC)CCCC.OB(O)O.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F Chemical compound CCCCN(CCCC)CCCC.CCCCN(CCCC)CCCC.CCCCN(CCCC)CCCC.OB(O)O.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F DPOMYQPPWKUQEK-UHFFFAOYSA-N 0.000 description 1
- UWKKBEQZACDEBT-UHFFFAOYSA-N CCCC[Mg] Chemical compound CCCC[Mg] UWKKBEQZACDEBT-UHFFFAOYSA-N 0.000 description 1
- PYZXFJMTFRQSQL-UHFFFAOYSA-N CCN(CC)CC.CCN(CC)CC.CCN(CC)CC.OB(O)O.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F Chemical compound CCN(CC)CC.CCN(CC)CC.CCN(CC)CC.OB(O)O.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F PYZXFJMTFRQSQL-UHFFFAOYSA-N 0.000 description 1
- KHMXZTDINUYUMM-UHFFFAOYSA-N CN(C)C.CN(C)C.CN(C)C.OB(O)O.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F Chemical compound CN(C)C.CN(C)C.CN(C)C.OB(O)O.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F KHMXZTDINUYUMM-UHFFFAOYSA-N 0.000 description 1
- RJWIFJATVBJLHT-UHFFFAOYSA-N C[Hf](C1C=CC=C1)(C1=CC=CC2=C1CC1=CC=CC=C21)[SiH2]C1=CC=CC=C1.Cl.Cl Chemical compound C[Hf](C1C=CC=C1)(C1=CC=CC2=C1CC1=CC=CC=C21)[SiH2]C1=CC=CC=C1.Cl.Cl RJWIFJATVBJLHT-UHFFFAOYSA-N 0.000 description 1
- WGJKGCQFGIMORT-UHFFFAOYSA-N C[SiH](C)C1=C(C=2CC3=C(C=CC=C3C2C=C1C(C)(C)C)C(C)(C)C)C1C=CC=C1 Chemical compound C[SiH](C)C1=C(C=2CC3=C(C=CC=C3C2C=C1C(C)(C)C)C(C)(C)C)C1C=CC=C1 WGJKGCQFGIMORT-UHFFFAOYSA-N 0.000 description 1
- CBNBXEOXXQZEII-UHFFFAOYSA-L C[SiH](C)[Hf](Cl)(Cl)(C1C=CC(=C1)[Si](C)(C)C)C1C=CC(=C1)[Si](C)(C)C Chemical compound C[SiH](C)[Hf](Cl)(Cl)(C1C=CC(=C1)[Si](C)(C)C)C1C=CC(=C1)[Si](C)(C)C CBNBXEOXXQZEII-UHFFFAOYSA-L 0.000 description 1
- VXKVHSOIPUVUIG-UHFFFAOYSA-N C[SiH](C)[Zr](C1=CC=CC=2C3=CC=CC=C3CC1=2)C1C=CC=C1 Chemical compound C[SiH](C)[Zr](C1=CC=CC=2C3=CC=CC=C3CC1=2)C1C=CC=C1 VXKVHSOIPUVUIG-UHFFFAOYSA-N 0.000 description 1
- UUWXZXQQDWGCFP-UHFFFAOYSA-L C[SiH](C)[Zr](Cl)(Cl)(C1C=C(C)C(C)=C1)C1C=C(C)C(C)=C1 Chemical compound C[SiH](C)[Zr](Cl)(Cl)(C1C=C(C)C(C)=C1)C1C=C(C)C(C)=C1 UUWXZXQQDWGCFP-UHFFFAOYSA-L 0.000 description 1
- IMNMCKQOOMHUAG-UHFFFAOYSA-L C[SiH](C)[Zr](Cl)(Cl)(C1C=CC(=C1)[Si](C)(C)C)C1C=CC(=C1)[Si](C)(C)C Chemical compound C[SiH](C)[Zr](Cl)(Cl)(C1C=CC(=C1)[Si](C)(C)C)C1C=CC(=C1)[Si](C)(C)C IMNMCKQOOMHUAG-UHFFFAOYSA-L 0.000 description 1
- GMTGXRNMOJWBPM-UHFFFAOYSA-N C[SiH](C1=CC=CC=C1)C1=C(C=2CC3=C(C=CC=C3C2C=C1C(C)(C)C)C(C)(C)C)C1C=CC=C1 Chemical compound C[SiH](C1=CC=CC=C1)C1=C(C=2CC3=C(C=CC=C3C2C=C1C(C)(C)C)C(C)(C)C)C1C=CC=C1 GMTGXRNMOJWBPM-UHFFFAOYSA-N 0.000 description 1
- SAKIGWJZTZKOAW-UHFFFAOYSA-N C[Si](C)(C)C(C=C1)=CC1[Hf](C)(C(C=C1)C=C1[Si](C)(C)C)[SiH2]C1=CC=CC=C1.Cl.Cl Chemical compound C[Si](C)(C)C(C=C1)=CC1[Hf](C)(C(C=C1)C=C1[Si](C)(C)C)[SiH2]C1=CC=CC=C1.Cl.Cl SAKIGWJZTZKOAW-UHFFFAOYSA-N 0.000 description 1
- YDUGOSCRXWZULO-UHFFFAOYSA-L C[Si](C)(C)C1=CC(C=C1)[Hf](Cl)(Cl)(=C)C1C=CC(=C1)[Si](C)(C)C Chemical compound C[Si](C)(C)C1=CC(C=C1)[Hf](Cl)(Cl)(=C)C1C=CC(=C1)[Si](C)(C)C YDUGOSCRXWZULO-UHFFFAOYSA-L 0.000 description 1
- VGVYFPUCSRFSOV-UHFFFAOYSA-L C[Si](C)(C)C1=CC(C=C1)[Zr](Cl)(Cl)(=C)C1C=CC(=C1)[Si](C)(C)C Chemical compound C[Si](C)(C)C1=CC(C=C1)[Zr](Cl)(Cl)(=C)C1C=CC(=C1)[Si](C)(C)C VGVYFPUCSRFSOV-UHFFFAOYSA-L 0.000 description 1
- ZJWSEPWXSAVQPE-UHFFFAOYSA-L C[Si](C)(C)C1=CC(C=C1)[Zr](Cl)(Cl)(C1C=CC(=C1)[Si](C)(C)C)[SiH](C1=CC=CC=C1)C1=CC=CC=C1 Chemical compound C[Si](C)(C)C1=CC(C=C1)[Zr](Cl)(Cl)(C1C=CC(=C1)[Si](C)(C)C)[SiH](C1=CC=CC=C1)C1=CC=CC=C1 ZJWSEPWXSAVQPE-UHFFFAOYSA-L 0.000 description 1
- LLSHAZJEPXLKBK-UHFFFAOYSA-N C[Si](C1=CC=C(C=C1)C(=C1C=CC=C1)C1=CC=C(C=C1)[Si](C)(C)C)(C)C Chemical compound C[Si](C1=CC=C(C=C1)C(=C1C=CC=C1)C1=CC=C(C=C1)[Si](C)(C)C)(C)C LLSHAZJEPXLKBK-UHFFFAOYSA-N 0.000 description 1
- HYXKBVWTHWPZNQ-UHFFFAOYSA-N C[Zr](C1C=CC=C1)(C1=CC=CC2=C1CC1=CC=CC=C21)[SiH2]C1=CC=CC=C1.Cl.Cl Chemical compound C[Zr](C1C=CC=C1)(C1=CC=CC2=C1CC1=CC=CC=C21)[SiH2]C1=CC=CC=C1.Cl.Cl HYXKBVWTHWPZNQ-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 description 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 1
- 239000004705 High-molecular-weight polyethylene Substances 0.000 description 1
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 1
- 239000004712 Metallocene polyethylene (PE-MC) Substances 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- XGEOKCMAPXEHEQ-UHFFFAOYSA-N OB(O)O.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.C(C=C1)=CC=C1P(C1=CC=CC=C1)C1=CC=CC=C1.C(C=C1)=CC=C1P(C1=CC=CC=C1)C1=CC=CC=C1.C(C=C1)=CC=C1P(C1=CC=CC=C1)C1=CC=CC=C1 Chemical compound OB(O)O.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.FC(C(C(C(F)=C(C(F)=C1F)F)=C1F)=C(C(F)=C1F)F)=C1F.C(C=C1)=CC=C1P(C1=CC=CC=C1)C1=CC=CC=C1.C(C=C1)=CC=C1P(C1=CC=CC=C1)C1=CC=CC=C1.C(C=C1)=CC=C1P(C1=CC=CC=C1)C1=CC=CC=C1 XGEOKCMAPXEHEQ-UHFFFAOYSA-N 0.000 description 1
- CQBWEBXPMRPCSI-UHFFFAOYSA-M O[Cr](O[SiH3])(=O)=O Chemical compound O[Cr](O[SiH3])(=O)=O CQBWEBXPMRPCSI-UHFFFAOYSA-M 0.000 description 1
- 239000002033 PVDF binder Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- 102000018779 Replication Protein C Human genes 0.000 description 1
- 108010027647 Replication Protein C Proteins 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 238000000944 Soxhlet extraction Methods 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 239000012963 UV stabilizer Substances 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 239000011954 Ziegler–Natta catalyst Substances 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- HXIWYNZXFFJFBW-HYXAFXHYSA-N [(Z)-4-oxopent-2-en-2-yl] hypochlorite Chemical compound CC(=O)\C=C(\C)OCl HXIWYNZXFFJFBW-HYXAFXHYSA-N 0.000 description 1
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 1
- HXEMAHFTVFVYMX-UHFFFAOYSA-M [Br-].CC[Ca+] Chemical compound [Br-].CC[Ca+] HXEMAHFTVFVYMX-UHFFFAOYSA-M 0.000 description 1
- KPLRDTLGVINSFD-UHFFFAOYSA-L [Cl-].[Cl-].C(C)(C)(C)C=1C=C(C=2CC3=C(C=CC=C3C2C1)C(C)(C)C)[Zr+2] Chemical compound [Cl-].[Cl-].C(C)(C)(C)C=1C=C(C=2CC3=C(C=CC=C3C2C1)C(C)(C)C)[Zr+2] KPLRDTLGVINSFD-UHFFFAOYSA-L 0.000 description 1
- UODXSUNCVXAZRY-UHFFFAOYSA-L [Cl-].[Cl-].C(C)(C)(C)C=1C=C(C=2CC3=C(C=CC=C3C=2C=1)C(C)(C)C)[Hf+2] Chemical compound [Cl-].[Cl-].C(C)(C)(C)C=1C=C(C=2CC3=C(C=CC=C3C=2C=1)C(C)(C)C)[Hf+2] UODXSUNCVXAZRY-UHFFFAOYSA-L 0.000 description 1
- FVAQUWYBIOUALD-UHFFFAOYSA-L [Cl-].[Cl-].C(C)(C)=[Zr+2](C1=CC(=CC=2C3=CC=CC(=C3CC1=2)C(C)(C)C)C(C)(C)C)C1C=CC=C1 Chemical compound [Cl-].[Cl-].C(C)(C)=[Zr+2](C1=CC(=CC=2C3=CC=CC(=C3CC1=2)C(C)(C)C)C(C)(C)C)C1C=CC=C1 FVAQUWYBIOUALD-UHFFFAOYSA-L 0.000 description 1
- YBRAFHPTROJHHK-UHFFFAOYSA-L [Cl-].[Cl-].C(C)[Si](C1=CC=C(C=C1)C(=[Hf+2](C1=CC=CC=2C3=CC=CC=C3CC1=2)C1C=CC=C1)C1=CC=C(C=C1)[Si](CC)(CC)CC)(CC)CC Chemical compound [Cl-].[Cl-].C(C)[Si](C1=CC=C(C=C1)C(=[Hf+2](C1=CC=CC=2C3=CC=CC=C3CC1=2)C1C=CC=C1)C1=CC=C(C=C1)[Si](CC)(CC)CC)(CC)CC YBRAFHPTROJHHK-UHFFFAOYSA-L 0.000 description 1
- MQZITAPHUVHZPR-UHFFFAOYSA-L [Cl-].[Cl-].C(C)[Si](C1=CC=C(C=C1)C(C1=CC=C(C=C1)[Si](CC)(CC)CC)=[Hf+2](C1=CC(=CC=2C3=CC=CC(=C3CC1=2)C(C)(C)C)C(C)(C)C)C1C=CC=C1)(CC)CC Chemical compound [Cl-].[Cl-].C(C)[Si](C1=CC=C(C=C1)C(C1=CC=C(C=C1)[Si](CC)(CC)CC)=[Hf+2](C1=CC(=CC=2C3=CC=CC(=C3CC1=2)C(C)(C)C)C(C)(C)C)C1C=CC=C1)(CC)CC MQZITAPHUVHZPR-UHFFFAOYSA-L 0.000 description 1
- RYMBHBRUKRKCOB-UHFFFAOYSA-L [Cl-].[Cl-].C(C)[Si](C1=CC=C(C=C1)C(C1=CC=C(C=C1)[Si](CC)(CC)CC)=[Zr+2](C1=CC(=CC=2C3=CC=CC(=C3CC1=2)C(C)(C)C)C(C)(C)C)C1C=CC=C1)(CC)CC Chemical compound [Cl-].[Cl-].C(C)[Si](C1=CC=C(C=C1)C(C1=CC=C(C=C1)[Si](CC)(CC)CC)=[Zr+2](C1=CC(=CC=2C3=CC=CC(=C3CC1=2)C(C)(C)C)C(C)(C)C)C1C=CC=C1)(CC)CC RYMBHBRUKRKCOB-UHFFFAOYSA-L 0.000 description 1
- HILIICNHOJSIPL-UHFFFAOYSA-L [Cl-].[Cl-].C1(=CC=CC=2C3=CC=CC=C3CC1=2)[Zr+2](C1C=CC=C1)=C Chemical compound [Cl-].[Cl-].C1(=CC=CC=2C3=CC=CC=C3CC1=2)[Zr+2](C1C=CC=C1)=C HILIICNHOJSIPL-UHFFFAOYSA-L 0.000 description 1
- VKQTWRYQMDWXCF-UHFFFAOYSA-L [Cl-].[Cl-].C1(=CC=CC=C1)C(C1=CC=CC=C1)=[Hf+2](C1=CC(=CC=2C3=CC=CC(=C3CC1=2)C(C)(C)C)C(C)(C)C)C1C=CC=C1 Chemical compound [Cl-].[Cl-].C1(=CC=CC=C1)C(C1=CC=CC=C1)=[Hf+2](C1=CC(=CC=2C3=CC=CC(=C3CC1=2)C(C)(C)C)C(C)(C)C)C1C=CC=C1 VKQTWRYQMDWXCF-UHFFFAOYSA-L 0.000 description 1
- VHEKIALTVUNQIH-UHFFFAOYSA-L [Cl-].[Cl-].C1(=CC=CC=C1)C(C1=CC=CC=C1)=[Hf+2](C1C=CC=C1)C1=CC=CC=2C3=CC=CC=C3CC1=2 Chemical compound [Cl-].[Cl-].C1(=CC=CC=C1)C(C1=CC=CC=C1)=[Hf+2](C1C=CC=C1)C1=CC=CC=2C3=CC=CC=C3CC1=2 VHEKIALTVUNQIH-UHFFFAOYSA-L 0.000 description 1
- IXTQUZWQWCRVKW-UHFFFAOYSA-L [Cl-].[Cl-].C1(=CC=CC=C1)[SiH](C1=CC=CC=C1)[Hf+2](C1=CC(=CC=2C3=CC=CC(=C3CC1=2)C(C)(C)C)C(C)(C)C)C1C=CC=C1 Chemical compound [Cl-].[Cl-].C1(=CC=CC=C1)[SiH](C1=CC=CC=C1)[Hf+2](C1=CC(=CC=2C3=CC=CC(=C3CC1=2)C(C)(C)C)C(C)(C)C)C1C=CC=C1 IXTQUZWQWCRVKW-UHFFFAOYSA-L 0.000 description 1
- GRNGBRGUTYBIRE-UHFFFAOYSA-L [Cl-].[Cl-].C1(=CC=CC=C1)[SiH](C1=CC=CC=C1)[Hf+2](C1C=CC=C1)C1=CC=CC=2C3=CC=CC=C3CC1=2 Chemical compound [Cl-].[Cl-].C1(=CC=CC=C1)[SiH](C1=CC=CC=C1)[Hf+2](C1C=CC=C1)C1=CC=CC=2C3=CC=CC=C3CC1=2 GRNGBRGUTYBIRE-UHFFFAOYSA-L 0.000 description 1
- AUXLPYVCGJWPFG-UHFFFAOYSA-L [Cl-].[Cl-].C1(=CC=CC=C1)[SiH](C1=CC=CC=C1)[Hf+2](C1CCC2CC=CC=C12)C1CCC2CC=CC=C12 Chemical compound [Cl-].[Cl-].C1(=CC=CC=C1)[SiH](C1=CC=CC=C1)[Hf+2](C1CCC2CC=CC=C12)C1CCC2CC=CC=C12 AUXLPYVCGJWPFG-UHFFFAOYSA-L 0.000 description 1
- CKDXKKAZNYCVDU-UHFFFAOYSA-L [Cl-].[Cl-].C1(=CC=CC=C1)[SiH](C1=CC=CC=C1)[Zr+2](C1=CC(=CC=2C3=CC=CC(=C3CC1=2)C(C)(C)C)C(C)(C)C)C1C=CC=C1 Chemical compound [Cl-].[Cl-].C1(=CC=CC=C1)[SiH](C1=CC=CC=C1)[Zr+2](C1=CC(=CC=2C3=CC=CC(=C3CC1=2)C(C)(C)C)C(C)(C)C)C1C=CC=C1 CKDXKKAZNYCVDU-UHFFFAOYSA-L 0.000 description 1
- YQRVWSCDBYGCDB-UHFFFAOYSA-L [Cl-].[Cl-].C1(=CC=CC=C1)[SiH](C1=CC=CC=C1)[Zr+2](C1=CC=CC=2C3=CC=CC=C3CC1=2)C1C=CC=C1 Chemical compound [Cl-].[Cl-].C1(=CC=CC=C1)[SiH](C1=CC=CC=C1)[Zr+2](C1=CC=CC=2C3=CC=CC=C3CC1=2)C1C=CC=C1 YQRVWSCDBYGCDB-UHFFFAOYSA-L 0.000 description 1
- MRDKKROLLLNPBH-UHFFFAOYSA-L [Cl-].[Cl-].C1(CCC2CC=CC=C12)[Hf+2] Chemical compound [Cl-].[Cl-].C1(CCC2CC=CC=C12)[Hf+2] MRDKKROLLLNPBH-UHFFFAOYSA-L 0.000 description 1
- RXTJYZGQYBJVSE-UHFFFAOYSA-L [Cl-].[Cl-].C1C2=CC=CC=C2C2=C1C([Zr+2])=CC=C2 Chemical compound [Cl-].[Cl-].C1C2=CC=CC=C2C2=C1C([Zr+2])=CC=C2 RXTJYZGQYBJVSE-UHFFFAOYSA-L 0.000 description 1
- QSZGOMRHQRFORD-UHFFFAOYSA-L [Cl-].[Cl-].C=C.C1=CC2=CC=CC=C2C1[Zr+2]C1C2=CC=CC=C2C=C1 Chemical compound [Cl-].[Cl-].C=C.C1=CC2=CC=CC=C2C1[Zr+2]C1C2=CC=CC=C2C=C1 QSZGOMRHQRFORD-UHFFFAOYSA-L 0.000 description 1
- RBAMZOPLQJJZLD-UHFFFAOYSA-L [Cl-].[Cl-].C=[Hf+2](C1=CC(=CC=2C3=CC=CC(=C3CC1=2)C(C)(C)C)C(C)(C)C)C1C=CC=C1 Chemical compound [Cl-].[Cl-].C=[Hf+2](C1=CC(=CC=2C3=CC=CC(=C3CC1=2)C(C)(C)C)C(C)(C)C)C1C=CC=C1 RBAMZOPLQJJZLD-UHFFFAOYSA-L 0.000 description 1
- VHKMACODXUOBET-UHFFFAOYSA-L [Cl-].[Cl-].C=[Hf+2](C1=CC=CC=2C3=CC=CC=C3CC1=2)C1C=CC=C1 Chemical compound [Cl-].[Cl-].C=[Hf+2](C1=CC=CC=2C3=CC=CC=C3CC1=2)C1C=CC=C1 VHKMACODXUOBET-UHFFFAOYSA-L 0.000 description 1
- RNGXLYVWHJFMBW-UHFFFAOYSA-L [Cl-].[Cl-].C=[Hf+2](C1C(=CC2=C(C=CC=C12)C1=CC=CC2=CC=CC=C12)C)C1C(=CC2=C(C=CC=C12)C1=CC=CC2=CC=CC=C12)C Chemical compound [Cl-].[Cl-].C=[Hf+2](C1C(=CC2=C(C=CC=C12)C1=CC=CC2=CC=CC=C12)C)C1C(=CC2=C(C=CC=C12)C1=CC=CC2=CC=CC=C12)C RNGXLYVWHJFMBW-UHFFFAOYSA-L 0.000 description 1
- AMYIOBGYBIXLFE-UHFFFAOYSA-L [Cl-].[Cl-].CC([SiH](C)[Zr+](C1C=CC2=C(C=CC(=C12)C)C)C1C=CC2=C(C=CC(=C12)C)C)C.C=[Hf](C1C(=CC2=C(C=CC=C12)C1=CC=CC=C1)C)C1C(=CC2=C(C=CC=C12)C1=CC=CC=C1)C.CC(C)[SiH](C)[Zr+](C1C=CC2=C(C=CC(=C12)C)C)C1C=CC2=C(C=CC(=C12)C)C Chemical compound [Cl-].[Cl-].CC([SiH](C)[Zr+](C1C=CC2=C(C=CC(=C12)C)C)C1C=CC2=C(C=CC(=C12)C)C)C.C=[Hf](C1C(=CC2=C(C=CC=C12)C1=CC=CC=C1)C)C1C(=CC2=C(C=CC=C12)C1=CC=CC=C1)C.CC(C)[SiH](C)[Zr+](C1C=CC2=C(C=CC(=C12)C)C)C1C=CC2=C(C=CC(=C12)C)C AMYIOBGYBIXLFE-UHFFFAOYSA-L 0.000 description 1
- LJTRHALOBDFJCT-UHFFFAOYSA-L [Cl-].[Cl-].CC1=CC(C(=CC=C2)C=3C=CC=CC=3)=C2C1[Zr+2](=C)C1C(C)=CC2=C1C=CC=C2C1=CC=CC=C1 Chemical compound [Cl-].[Cl-].CC1=CC(C(=CC=C2)C=3C=CC=CC=3)=C2C1[Zr+2](=C)C1C(C)=CC2=C1C=CC=C2C1=CC=CC=C1 LJTRHALOBDFJCT-UHFFFAOYSA-L 0.000 description 1
- UDPQUWPUPHBEKR-UHFFFAOYSA-L [Cl-].[Cl-].CC1=Cc2c(cccc2-c2ccccc2)C1[Zr++]1(CC1)C1C(C)=Cc2c1cccc2-c1ccccc1 Chemical compound [Cl-].[Cl-].CC1=Cc2c(cccc2-c2ccccc2)C1[Zr++]1(CC1)C1C(C)=Cc2c1cccc2-c1ccccc1 UDPQUWPUPHBEKR-UHFFFAOYSA-L 0.000 description 1
- IOBGXXQUZFZDNL-UHFFFAOYSA-L [Cl-].[Cl-].CC1=Cc2ccccc2C1[Hf++] Chemical compound [Cl-].[Cl-].CC1=Cc2ccccc2C1[Hf++] IOBGXXQUZFZDNL-UHFFFAOYSA-L 0.000 description 1
- YXIARWMBTNXPAN-UHFFFAOYSA-L [Cl-].[Cl-].CC=1C(=C(C=CC1)[SiH](C1=CC=CC=C1)[Hf+](C1CCC2CC=CC=C12)C1CCC2CC=CC=C12)C.C[SiH](C)[Hf+](C1CCC2CC=CC=C12)C1CCC2CC=CC=C12 Chemical compound [Cl-].[Cl-].CC=1C(=C(C=CC1)[SiH](C1=CC=CC=C1)[Hf+](C1CCC2CC=CC=C12)C1CCC2CC=CC=C12)C.C[SiH](C)[Hf+](C1CCC2CC=CC=C12)C1CCC2CC=CC=C12 YXIARWMBTNXPAN-UHFFFAOYSA-L 0.000 description 1
- HMAVCOLCFIQXFY-UHFFFAOYSA-L [Cl-].[Cl-].CC=1C(C=CC1C)[Hf+2]C1C(=C(C=C1)C)C.C=C Chemical compound [Cl-].[Cl-].CC=1C(C=CC1C)[Hf+2]C1C(=C(C=C1)C)C.C=C HMAVCOLCFIQXFY-UHFFFAOYSA-L 0.000 description 1
- VOESPWUATJENDM-UHFFFAOYSA-L [Cl-].[Cl-].C[SiH](C)[Hf+2](C1(C(=CC=C1)C)C)C1(C(=CC=C1)C)C Chemical compound [Cl-].[Cl-].C[SiH](C)[Hf+2](C1(C(=CC=C1)C)C)C1(C(=CC=C1)C)C VOESPWUATJENDM-UHFFFAOYSA-L 0.000 description 1
- HSDXADAAUWWOID-UHFFFAOYSA-L [Cl-].[Cl-].C[SiH](C)[Hf+2](C1=CC(=CC=2C3=CC=CC(=C3CC1=2)C(C)(C)C)C(C)(C)C)C1C=CC=C1 Chemical compound [Cl-].[Cl-].C[SiH](C)[Hf+2](C1=CC(=CC=2C3=CC=CC(=C3CC1=2)C(C)(C)C)C(C)(C)C)C1C=CC=C1 HSDXADAAUWWOID-UHFFFAOYSA-L 0.000 description 1
- BKOOEHXKLPZJJD-UHFFFAOYSA-L [Cl-].[Cl-].C[SiH](C)[Hf+2](C1C=CC=C1)C1=CC=CC=2C3=CC=CC=C3CC1=2 Chemical compound [Cl-].[Cl-].C[SiH](C)[Hf+2](C1C=CC=C1)C1=CC=CC=2C3=CC=CC=C3CC1=2 BKOOEHXKLPZJJD-UHFFFAOYSA-L 0.000 description 1
- UGNWROHEQRMYIC-UHFFFAOYSA-L [Cl-].[Cl-].C[SiH](C)[Ti+2](C1C=CC=C1)C1=CC=CC=2C3=CC=CC=C3CC1=2 Chemical compound [Cl-].[Cl-].C[SiH](C)[Ti+2](C1C=CC=C1)C1=CC=CC=2C3=CC=CC=C3CC1=2 UGNWROHEQRMYIC-UHFFFAOYSA-L 0.000 description 1
- SRDOMKALHPEHIJ-UHFFFAOYSA-L [Cl-].[Cl-].C[SiH](C)[Zr+2](C1=CC=CC=2C3=CC=CC=C3CC1=2)C1C=CC=C1 Chemical compound [Cl-].[Cl-].C[SiH](C)[Zr+2](C1=CC=CC=2C3=CC=CC=C3CC1=2)C1C=CC=C1 SRDOMKALHPEHIJ-UHFFFAOYSA-L 0.000 description 1
- WBAJYANTFNXRNW-UHFFFAOYSA-L [Cl-].[Cl-].C[Si](C1=CC=C(C=C1)C(=[Hf+2](C1=CC(=CC=2C3=CC=CC(=C3CC1=2)C(C)(C)C)C(C)(C)C)C1C=CC=C1)C1=CC=C(C=C1)[Si](C)(C)C)(C)C Chemical compound [Cl-].[Cl-].C[Si](C1=CC=C(C=C1)C(=[Hf+2](C1=CC(=CC=2C3=CC=CC(=C3CC1=2)C(C)(C)C)C(C)(C)C)C1C=CC=C1)C1=CC=C(C=C1)[Si](C)(C)C)(C)C WBAJYANTFNXRNW-UHFFFAOYSA-L 0.000 description 1
- DMFRITURMMKHHI-UHFFFAOYSA-L [Cl-].[Cl-].C[Si](C1=CC=C(C=C1)C(=[Hf+2](C1=CC=CC=2C3=CC=CC=C3CC1=2)C1C=CC=C1)C1=CC=C(C=C1)[Si](C)(C)C)(C)C Chemical compound [Cl-].[Cl-].C[Si](C1=CC=C(C=C1)C(=[Hf+2](C1=CC=CC=2C3=CC=CC=C3CC1=2)C1C=CC=C1)C1=CC=C(C=C1)[Si](C)(C)C)(C)C DMFRITURMMKHHI-UHFFFAOYSA-L 0.000 description 1
- JKHTYQNHUHBBRL-UHFFFAOYSA-L [Cl-].[Cl-].C[Si](C1=CC=C(C=C1)C(=[Zr+2](C1=CC=CC=2C3=CC=CC=C3CC1=2)C1C=CC=C1)C1=CC=C(C=C1)[Si](C)(C)C)(C)C Chemical compound [Cl-].[Cl-].C[Si](C1=CC=C(C=C1)C(=[Zr+2](C1=CC=CC=2C3=CC=CC=C3CC1=2)C1C=CC=C1)C1=CC=C(C=C1)[Si](C)(C)C)(C)C JKHTYQNHUHBBRL-UHFFFAOYSA-L 0.000 description 1
- YBDQDJQQEJJFPS-UHFFFAOYSA-L [Cl-].[Cl-].Cc1ccc(C)c2[C@H](C=Cc12)[Zr++]1(CC1)[C@@H]1C=Cc2c1c(C)ccc2C Chemical compound [Cl-].[Cl-].Cc1ccc(C)c2[C@H](C=Cc12)[Zr++]1(CC1)[C@@H]1C=Cc2c1c(C)ccc2C YBDQDJQQEJJFPS-UHFFFAOYSA-L 0.000 description 1
- SQZAWSJHEQUYIV-UHFFFAOYSA-L [Cl-].[Cl-].[Ti+3].C=C1C2(CC3CC(CC1C3)C2)[N-]C2(C(=C(C(=C2)C)C)C)C Chemical compound [Cl-].[Cl-].[Ti+3].C=C1C2(CC3CC(CC1C3)C2)[N-]C2(C(=C(C(=C2)C)C)C)C SQZAWSJHEQUYIV-UHFFFAOYSA-L 0.000 description 1
- NWZXKRNRRQFCPW-UHFFFAOYSA-L [Cl-].[Cl-].[Ti+3].CC=1C(=C(C(C1)(C)[N-]C1CCCCC1)C)C.C=C Chemical compound [Cl-].[Cl-].[Ti+3].CC=1C(=C(C(C1)(C)[N-]C1CCCCC1)C)C.C=C NWZXKRNRRQFCPW-UHFFFAOYSA-L 0.000 description 1
- HRSDXFQCPONVQK-UHFFFAOYSA-L [Cl-].[Cl-].[Ti+3].CC=1C(=C(C(C1)(C)[N-]C1CCCCCCCCCCC1)C)C.C=C Chemical compound [Cl-].[Cl-].[Ti+3].CC=1C(=C(C(C1)(C)[N-]C1CCCCCCCCCCC1)C)C.C=C HRSDXFQCPONVQK-UHFFFAOYSA-L 0.000 description 1
- IWNLEGOLOGYVSO-UHFFFAOYSA-L [Cl-].[Cl-].[Ti+3].C[SiH](C)C1(CCCCC1)[N-]C1C(=CC=C1C)C Chemical compound [Cl-].[Cl-].[Ti+3].C[SiH](C)C1(CCCCC1)[N-]C1C(=CC=C1C)C IWNLEGOLOGYVSO-UHFFFAOYSA-L 0.000 description 1
- BXASICAXCQNLJF-UHFFFAOYSA-L [Cl-].[Cl-].[Ti+3].C[SiH](C)C1(CCCCC1)[N-]C1C(=CC=C1C)CC Chemical compound [Cl-].[Cl-].[Ti+3].C[SiH](C)C1(CCCCC1)[N-]C1C(=CC=C1C)CC BXASICAXCQNLJF-UHFFFAOYSA-L 0.000 description 1
- BUJVGCYHYGYVRO-UHFFFAOYSA-L [Cl-].[Cl-].[Ti+3].C[SiH](C)C1(CCCCCCCCCCC1)[N-]C1(C(=C(C(=C1)C)C)C)C Chemical compound [Cl-].[Cl-].[Ti+3].C[SiH](C)C1(CCCCCCCCCCC1)[N-]C1(C(=C(C(=C1)C)C)C)C BUJVGCYHYGYVRO-UHFFFAOYSA-L 0.000 description 1
- JVJWGFXOMGYYQU-UHFFFAOYSA-L [Cl-].[Cl-].[Ti+3].C[SiH](C)C1(CCCCCCCCCCC1)[N-]C1C(=CC=C1C)C Chemical compound [Cl-].[Cl-].[Ti+3].C[SiH](C)C1(CCCCCCCCCCC1)[N-]C1C(=CC=C1C)C JVJWGFXOMGYYQU-UHFFFAOYSA-L 0.000 description 1
- NRGLDSXBKLJCRY-UHFFFAOYSA-L [Cl-].[Cl-].[Ti+3].C[SiH](C)C1C2(CC3CC(CC1C3)C2)[N-]C2C(=CC=C2C)CC Chemical compound [Cl-].[Cl-].[Ti+3].C[SiH](C)C1C2(CC3CC(CC1C3)C2)[N-]C2C(=CC=C2C)CC NRGLDSXBKLJCRY-UHFFFAOYSA-L 0.000 description 1
- LNKNUAVVTPSYIK-UHFFFAOYSA-N [Cl].[Cl].[Zr] Chemical compound [Cl].[Cl].[Zr] LNKNUAVVTPSYIK-UHFFFAOYSA-N 0.000 description 1
- YRZNWDHYROIEKQ-UHFFFAOYSA-N [Hf++].C[O-].C[O-] Chemical compound [Hf++].C[O-].C[O-] YRZNWDHYROIEKQ-UHFFFAOYSA-N 0.000 description 1
- OLBVUFHMDRJKTK-UHFFFAOYSA-N [N].[O] Chemical compound [N].[O] OLBVUFHMDRJKTK-UHFFFAOYSA-N 0.000 description 1
- ONBAMSNXTDLAKO-UHFFFAOYSA-N [Ti].[CH2][CH2].C[C]1[C](C)[C](C)[C](C)[C]1C.C[C]1[C](C)[C](C)[C](C)[C]1C Chemical group [Ti].[CH2][CH2].C[C]1[C](C)[C](C)[C](C)[C]1C.C[C]1[C](C)[C](C)[C](C)[C]1C ONBAMSNXTDLAKO-UHFFFAOYSA-N 0.000 description 1
- LQOCWQSEBCRDJB-UHFFFAOYSA-N [Zr].C1(C=CC=C1)C(C(=C)C1C=CC=C1)=C Chemical compound [Zr].C1(C=CC=C1)C(C(=C)C1C=CC=C1)=C LQOCWQSEBCRDJB-UHFFFAOYSA-N 0.000 description 1
- OBMKVFCJTIRLJW-UHFFFAOYSA-N [Zr].C1(C=CC=C1)C=C(C(=CC1C=CC=C1)C)C Chemical compound [Zr].C1(C=CC=C1)C=C(C(=CC1C=CC=C1)C)C OBMKVFCJTIRLJW-UHFFFAOYSA-N 0.000 description 1
- XVQZDTAAAJOLSB-UHFFFAOYSA-N [Zr].CC1=C(C(=C(C1(C)C1=C(C=CC=C1)C1(C(=C(C(=C1C)C)C)C)C)C)C)C Chemical compound [Zr].CC1=C(C(=C(C1(C)C1=C(C=CC=C1)C1(C(=C(C(=C1C)C)C)C)C)C)C)C XVQZDTAAAJOLSB-UHFFFAOYSA-N 0.000 description 1
- 229920006397 acrylic thermoplastic Polymers 0.000 description 1
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000002313 adhesive film Substances 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 239000004964 aerogel Substances 0.000 description 1
- 239000012615 aggregate Substances 0.000 description 1
- 150000007824 aliphatic compounds Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000005234 alkyl aluminium group Chemical group 0.000 description 1
- 125000005115 alkyl carbamoyl group Chemical group 0.000 description 1
- 125000004414 alkyl thio group Chemical group 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000012683 anionic precursor Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 238000000149 argon plasma sintering Methods 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 150000001502 aryl halides Chemical class 0.000 description 1
- 150000005840 aryl radicals Chemical class 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- ZIQCCIAIROIHHR-UHFFFAOYSA-N benzene;boric acid Chemical compound OB(O)O.C1=CC=CC=C1 ZIQCCIAIROIHHR-UHFFFAOYSA-N 0.000 description 1
- 229910052790 beryllium Inorganic materials 0.000 description 1
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 1
- LWBPNIJBHRISSS-UHFFFAOYSA-L beryllium chloride Substances Cl[Be]Cl LWBPNIJBHRISSS-UHFFFAOYSA-L 0.000 description 1
- 229910001627 beryllium chloride Inorganic materials 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- AZWXAPCAJCYGIA-UHFFFAOYSA-N bis(2-methylpropyl)alumane Chemical compound CC(C)C[AlH]CC(C)C AZWXAPCAJCYGIA-UHFFFAOYSA-N 0.000 description 1
- 239000002981 blocking agent Substances 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- JKFJJYOIWGFQGI-UHFFFAOYSA-M bromo-bis(2-methylpropyl)alumane Chemical compound [Br-].CC(C)C[Al+]CC(C)C JKFJJYOIWGFQGI-UHFFFAOYSA-M 0.000 description 1
- INLLPKCGLOXCIV-UHFFFAOYSA-N bromoethene Chemical compound BrC=C INLLPKCGLOXCIV-UHFFFAOYSA-N 0.000 description 1
- PBGVMIDTGGTBFS-UHFFFAOYSA-N but-3-enylbenzene Chemical compound C=CCCC1=CC=CC=C1 PBGVMIDTGGTBFS-UHFFFAOYSA-N 0.000 description 1
- 125000004369 butenyl group Chemical group C(=CCC)* 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- OCFSGVNHPVWWKD-UHFFFAOYSA-N butylaluminum Chemical compound [Al].[CH2]CCC OCFSGVNHPVWWKD-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 description 1
- 125000005517 carbenium group Chemical group 0.000 description 1
- 125000005626 carbonium group Chemical group 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000011951 cationic catalyst Substances 0.000 description 1
- 238000010538 cationic polymerization reaction Methods 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000012986 chain transfer agent Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 125000004803 chlorobenzyl group Chemical group 0.000 description 1
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 description 1
- 229960001231 choline Drugs 0.000 description 1
- TYYBBNOTQFVVKN-UHFFFAOYSA-N chromium(2+);cyclopenta-1,3-diene Chemical compound [Cr+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 TYYBBNOTQFVVKN-UHFFFAOYSA-N 0.000 description 1
- MJSNUBOCVAKFIJ-LNTINUHCSA-N chromium;(z)-4-oxoniumylidenepent-2-en-2-olate Chemical compound [Cr].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O MJSNUBOCVAKFIJ-LNTINUHCSA-N 0.000 description 1
- NPCUWXDZFXSRLT-UHFFFAOYSA-N chromium;2-ethylhexanoic acid Chemical compound [Cr].CCCCC(CC)C(O)=O NPCUWXDZFXSRLT-UHFFFAOYSA-N 0.000 description 1
- XEHUIDSUOAGHBW-UHFFFAOYSA-N chromium;pentane-2,4-dione Chemical compound [Cr].CC(=O)CC(C)=O.CC(=O)CC(C)=O.CC(=O)CC(C)=O XEHUIDSUOAGHBW-UHFFFAOYSA-N 0.000 description 1
- AHXGRMIPHCAXFP-UHFFFAOYSA-L chromyl dichloride Chemical compound Cl[Cr](Cl)(=O)=O AHXGRMIPHCAXFP-UHFFFAOYSA-L 0.000 description 1
- 229930016911 cinnamic acid Natural products 0.000 description 1
- 235000013985 cinnamic acid Nutrition 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 239000004595 color masterbatch Substances 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 239000012050 conventional carrier Substances 0.000 description 1
- 150000004696 coordination complex Chemical class 0.000 description 1
- 238000012718 coordination polymerization Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 229920003020 cross-linked polyethylene Polymers 0.000 description 1
- 239000004703 cross-linked polyethylene Substances 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 125000000392 cycloalkenyl group Chemical group 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- CFBGXYDUODCMNS-UHFFFAOYSA-N cyclobutene Chemical compound C1CC=C1 CFBGXYDUODCMNS-UHFFFAOYSA-N 0.000 description 1
- WAHYKMNUOGZJNU-UHFFFAOYSA-L cyclododecylazanide titanium(3+) dichloride Chemical compound [Cl-].[Cl-].C1(CCCCCCCCCCC1)N[Ti+2] WAHYKMNUOGZJNU-UHFFFAOYSA-L 0.000 description 1
- GJRPEZCBSXLLJN-UHFFFAOYSA-N cyclopenta-1,3-dien-1-yl(dimethyl)silane Chemical compound C[SiH](C)C1=CC=CC1 GJRPEZCBSXLLJN-UHFFFAOYSA-N 0.000 description 1
- XOVJAYNMQDTIJD-UHFFFAOYSA-N cyclopentobarbital Chemical compound C1CC=CC1C1(CC=C)C(=O)NC(=O)NC1=O XOVJAYNMQDTIJD-UHFFFAOYSA-N 0.000 description 1
- 230000009849 deactivation Effects 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 125000005131 dialkylammonium group Chemical group 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- UZVGSSNIUNSOFA-UHFFFAOYSA-N dibenzofuran-1-carboxylic acid Chemical compound O1C2=CC=CC=C2C2=C1C=CC=C2C(=O)O UZVGSSNIUNSOFA-UHFFFAOYSA-N 0.000 description 1
- WWPSJFCVFWMRBH-UHFFFAOYSA-L dibromoalumane Chemical compound Br[AlH]Br WWPSJFCVFWMRBH-UHFFFAOYSA-L 0.000 description 1
- PDZFAAAZGSZIFN-UHFFFAOYSA-N dichloro(2-methylpropyl)borane Chemical compound CC(C)CB(Cl)Cl PDZFAAAZGSZIFN-UHFFFAOYSA-N 0.000 description 1
- LHCGBIFHSCCRRG-UHFFFAOYSA-N dichloroborane Chemical compound ClBCl LHCGBIFHSCCRRG-UHFFFAOYSA-N 0.000 description 1
- XBPCUCUWBYBCDP-UHFFFAOYSA-O dicyclohexylazanium Chemical compound C1CCCCC1[NH2+]C1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-O 0.000 description 1
- LJSQFQKUNVCTIA-UHFFFAOYSA-N diethyl sulfide Chemical class CCSCC LJSQFQKUNVCTIA-UHFFFAOYSA-N 0.000 description 1
- YNLAOSYQHBDIKW-UHFFFAOYSA-M diethylaluminium chloride Chemical compound CC[Al](Cl)CC YNLAOSYQHBDIKW-UHFFFAOYSA-M 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- FAFYLCKQPJOORN-UHFFFAOYSA-N diethylborane Chemical compound CCBCC FAFYLCKQPJOORN-UHFFFAOYSA-N 0.000 description 1
- HQWPLXHWEZZGKY-UHFFFAOYSA-N diethylzinc Chemical compound CC[Zn]CC HQWPLXHWEZZGKY-UHFFFAOYSA-N 0.000 description 1
- 125000006001 difluoroethyl group Chemical group 0.000 description 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 1
- GXCQMKSGALTBLC-UHFFFAOYSA-N dihexylmercury Chemical compound CCCCCC[Hg]CCCCCC GXCQMKSGALTBLC-UHFFFAOYSA-N 0.000 description 1
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- UUMKDFIEIRWWBX-UHFFFAOYSA-N dimethyl-(2,3,4,5-tetramethylcyclopenta-2,4-dien-1-yl)silane Chemical compound C[SiH](C)C1C(C)=C(C)C(C)=C1C UUMKDFIEIRWWBX-UHFFFAOYSA-N 0.000 description 1
- QKIUAMUSENSFQQ-UHFFFAOYSA-N dimethylazanide Chemical compound C[N-]C QKIUAMUSENSFQQ-UHFFFAOYSA-N 0.000 description 1
- ZTJBELXDHFJJEU-UHFFFAOYSA-N dimethylboron Chemical compound C[B]C ZTJBELXDHFJJEU-UHFFFAOYSA-N 0.000 description 1
- YOTZYFSGUCFUKA-UHFFFAOYSA-N dimethylphosphine Chemical compound CPC YOTZYFSGUCFUKA-UHFFFAOYSA-N 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- GPAYUJZHTULNBE-UHFFFAOYSA-N diphenylphosphine Chemical compound C=1C=CC=CC=1PC1=CC=CC=C1 GPAYUJZHTULNBE-UHFFFAOYSA-N 0.000 description 1
- WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 238000006056 electrooxidation reaction Methods 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- HGVPOWOAHALJHA-UHFFFAOYSA-N ethene;methyl prop-2-enoate Chemical compound C=C.COC(=O)C=C HGVPOWOAHALJHA-UHFFFAOYSA-N 0.000 description 1
- GCSJLQSCSDMKTP-UHFFFAOYSA-N ethenyl(trimethyl)silane Chemical compound C[Si](C)(C)C=C GCSJLQSCSDMKTP-UHFFFAOYSA-N 0.000 description 1
- LDLDYFCCDKENPD-UHFFFAOYSA-N ethenylcyclohexane Chemical compound C=CC1CCCCC1 LDLDYFCCDKENPD-UHFFFAOYSA-N 0.000 description 1
- OYCNHLAKDKIJIT-UHFFFAOYSA-N ethyl-bis(2-methylpropyl)borane Chemical compound CC(C)CB(CC)CC(C)C OYCNHLAKDKIJIT-UHFFFAOYSA-N 0.000 description 1
- 229920006225 ethylene-methyl acrylate Polymers 0.000 description 1
- 239000005043 ethylene-methyl acrylate Substances 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 238000004299 exfoliation Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000000834 fixative Substances 0.000 description 1
- RMBPEFMHABBEKP-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2C3=C[CH]C=CC3=CC2=C1 RMBPEFMHABBEKP-UHFFFAOYSA-N 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 1
- 125000003784 fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 description 1
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000013467 fragmentation Methods 0.000 description 1
- 238000006062 fragmentation reaction Methods 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- 239000013538 functional additive Substances 0.000 description 1
- 238000007306 functionalization reaction Methods 0.000 description 1
- 230000008570 general process Effects 0.000 description 1
- 229910021482 group 13 metal Inorganic materials 0.000 description 1
- 229910021436 group 13–16 element Inorganic materials 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 229920005555 halobutyl Polymers 0.000 description 1
- 125000004968 halobutyl group Chemical group 0.000 description 1
- YLQFLHWATWECNM-UHFFFAOYSA-N heptacosa-1,3-diene Chemical compound CCCCCCCCCCCCCCCCCCCCCCCC=CC=C YLQFLHWATWECNM-UHFFFAOYSA-N 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000003936 heterocyclopentadienyl group Chemical group 0.000 description 1
- AHAREKHAZNPPMI-UHFFFAOYSA-N hexa-1,3-diene Chemical compound CCC=CC=C AHAREKHAZNPPMI-UHFFFAOYSA-N 0.000 description 1
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical compound C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 150000002466 imines Chemical class 0.000 description 1
- 230000003100 immobilizing effect Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- 229910001504 inorganic chloride Inorganic materials 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- ICIWUVCWSCSTAQ-UHFFFAOYSA-N iodic acid Chemical class OI(=O)=O ICIWUVCWSCSTAQ-UHFFFAOYSA-N 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000000654 isopropylidene group Chemical group C(C)(C)=* 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- 150000002576 ketones Chemical group 0.000 description 1
- 235000001510 limonene Nutrition 0.000 description 1
- 229940087305 limonene Drugs 0.000 description 1
- 229920000092 linear low density polyethylene Polymers 0.000 description 1
- 239000004707 linear low-density polyethylene Substances 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000006166 lysate Substances 0.000 description 1
- 150000002678 macrocyclic compounds Chemical class 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CCERQOYLJJULMD-UHFFFAOYSA-M magnesium;carbanide;chloride Chemical compound [CH3-].[Mg+2].[Cl-] CCERQOYLJJULMD-UHFFFAOYSA-M 0.000 description 1
- 229920001179 medium density polyethylene Polymers 0.000 description 1
- 239000004701 medium-density polyethylene Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- RTWNYYOXLSILQN-UHFFFAOYSA-N methanediamine Chemical compound NCN RTWNYYOXLSILQN-UHFFFAOYSA-N 0.000 description 1
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
- MHERPFVRWOTBSF-UHFFFAOYSA-N methyl(phenyl)phosphane Chemical compound CPC1=CC=CC=C1 MHERPFVRWOTBSF-UHFFFAOYSA-N 0.000 description 1
- NFWSQSCIDYBUOU-UHFFFAOYSA-N methylcyclopentadiene Chemical compound CC1=CC=CC1 NFWSQSCIDYBUOU-UHFFFAOYSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- DVSDBMFJEQPWNO-UHFFFAOYSA-N methyllithium Chemical compound C[Li] DVSDBMFJEQPWNO-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 238000000569 multi-angle light scattering Methods 0.000 description 1
- WXFNPHZNUUIRFT-UHFFFAOYSA-N n',n'-diethyl-n-phenylpropane-1,3-diamine Chemical compound CCN(CC)CCCNC1=CC=CC=C1 WXFNPHZNUUIRFT-UHFFFAOYSA-N 0.000 description 1
- PHQOGHDTIVQXHL-UHFFFAOYSA-N n'-(3-trimethoxysilylpropyl)ethane-1,2-diamine Chemical compound CO[Si](OC)(OC)CCCNCCN PHQOGHDTIVQXHL-UHFFFAOYSA-N 0.000 description 1
- OXQMIXBVXHWDPX-UHFFFAOYSA-N n,n,2-trimethylpropan-2-amine Chemical compound CN(C)C(C)(C)C OXQMIXBVXHWDPX-UHFFFAOYSA-N 0.000 description 1
- SRLHDBRENZFCIN-UHFFFAOYSA-N n,n-di(butan-2-yl)butan-2-amine Chemical compound CCC(C)N(C(C)CC)C(C)CC SRLHDBRENZFCIN-UHFFFAOYSA-N 0.000 description 1
- DYFFAVRFJWYYQO-UHFFFAOYSA-N n-methyl-n-phenylaniline Chemical compound C=1C=CC=CC=1N(C)C1=CC=CC=C1 DYFFAVRFJWYYQO-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000002114 nanocomposite Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 1
- 238000005580 one pot reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-O oxonium Chemical compound [OH3+] XLYOFNOQVPJJNP-UHFFFAOYSA-O 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- QYZLKGVUSQXAMU-UHFFFAOYSA-N penta-1,4-diene Chemical compound C=CCC=C QYZLKGVUSQXAMU-UHFFFAOYSA-N 0.000 description 1
- GUVXZFRDPCKWEM-UHFFFAOYSA-N pentalene Chemical compound C1=CC2=CC=CC2=C1 GUVXZFRDPCKWEM-UHFFFAOYSA-N 0.000 description 1
- 125000002097 pentamethylcyclopentadienyl group Chemical group 0.000 description 1
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical class OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
- 125000005062 perfluorophenyl group Chemical group FC1=C(C(=C(C(=C1F)F)F)F)* 0.000 description 1
- KHIWWQKSHDUIBK-UHFFFAOYSA-N periodic acid Chemical class OI(=O)(=O)=O KHIWWQKSHDUIBK-UHFFFAOYSA-N 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 239000002530 phenolic antioxidant Substances 0.000 description 1
- JBLSZOJIKAQEKG-UHFFFAOYSA-N phenyl hypobromite Chemical compound BrOC1=CC=CC=C1 JBLSZOJIKAQEKG-UHFFFAOYSA-N 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- 125000005498 phthalate group Chemical class 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 229910052615 phyllosilicate Inorganic materials 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 150000004291 polyenes Chemical class 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 238000010094 polymer processing Methods 0.000 description 1
- 230000037048 polymerization activity Effects 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 229920006380 polyphenylene oxide Polymers 0.000 description 1
- 229920003053 polystyrene-divinylbenzene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- 150000004032 porphyrins Chemical class 0.000 description 1
- KBGJIKKXNIQHQH-UHFFFAOYSA-N potassium;methanidylbenzene Chemical compound [K+].[CH2-]C1=CC=CC=C1 KBGJIKKXNIQHQH-UHFFFAOYSA-N 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 1
- 229920005604 random copolymer Polymers 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229920006126 semicrystalline polymer Polymers 0.000 description 1
- 238000012486 side-by-side testing Methods 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 238000000935 solvent evaporation Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229920006132 styrene block copolymer Polymers 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 229910052714 tellurium Inorganic materials 0.000 description 1
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- RAOIDOHSFRTOEL-UHFFFAOYSA-N tetrahydrothiophene Chemical compound C1CCSC1 RAOIDOHSFRTOEL-UHFFFAOYSA-N 0.000 description 1
- 238000012719 thermal polymerization Methods 0.000 description 1
- 229920006345 thermoplastic polyamide Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- UIERETOOQGIECD-ONEGZZNKSA-N tiglic acid Chemical compound C\C=C(/C)C(O)=O UIERETOOQGIECD-ONEGZZNKSA-N 0.000 description 1
- PMTRSEDNJGMXLN-UHFFFAOYSA-N titanium zirconium Chemical compound [Ti].[Zr] PMTRSEDNJGMXLN-UHFFFAOYSA-N 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 238000006276 transfer reaction Methods 0.000 description 1
- RXJKFRMDXUJTEX-UHFFFAOYSA-N triethylphosphine Chemical compound CCP(CC)CC RXJKFRMDXUJTEX-UHFFFAOYSA-N 0.000 description 1
- RERMPCBBVZEPBS-UHFFFAOYSA-N tris(2,6-dimethylphenyl)phosphane Chemical compound CC1=CC=CC(C)=C1P(C=1C(=CC=CC=1C)C)C1=C(C)C=CC=C1C RERMPCBBVZEPBS-UHFFFAOYSA-N 0.000 description 1
- COIOYMYWGDAQPM-UHFFFAOYSA-N tris(2-methylphenyl)phosphane Chemical compound CC1=CC=CC=C1P(C=1C(=CC=CC=1)C)C1=CC=CC=C1C COIOYMYWGDAQPM-UHFFFAOYSA-N 0.000 description 1
- 229920001862 ultra low molecular weight polyethylene Polymers 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 238000003828 vacuum filtration Methods 0.000 description 1
- 125000005287 vanadyl group Chemical group 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000003643 water by type Substances 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
- 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
-
- 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
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/04—Monomers containing three or four carbon atoms
- C08F210/06—Propene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- 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
- C08F110/00—Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F110/04—Monomers containing three or four carbon atoms
- C08F110/06—Propene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2420/00—Metallocene catalysts
- C08F2420/10—Heteroatom-substituted bridge, i.e. Cp or analog where the bridge linking the two Cps or analogs is substituted by at least one group that contains a heteroatom
-
- 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
- C08F4/65922—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 containing at least two cyclopentadienyl rings, fused or not
- C08F4/65927—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 containing at least two cyclopentadienyl rings, fused or not two cyclopentadienyl rings being mutually bridged
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S526/943—Polymerization with metallocene catalysts
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)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/825,380 US7223822B2 (en) | 2002-10-15 | 2004-04-15 | Multiple catalyst and reactor system for olefin polymerization and polymers produced therefrom |
| US10/825,380 | 2004-04-15 | ||
| PCT/US2005/012721 WO2005113622A1 (en) | 2004-04-15 | 2005-04-13 | Multiple catalyst and reactor system for olefin polymerization and polymers produced therefrom |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2007532762A JP2007532762A (ja) | 2007-11-15 |
| JP2007532762A5 JP2007532762A5 (https=) | 2008-06-05 |
| JP5348732B2 true JP5348732B2 (ja) | 2013-11-20 |
Family
ID=35004326
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007508539A Expired - Fee Related JP5348732B2 (ja) | 2004-04-15 | 2005-04-13 | オレフィン重合およびそれにより生成されるポリマーのための多種触媒および反応装置システム |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US7223822B2 (https=) |
| EP (1) | EP1753796B1 (https=) |
| JP (1) | JP5348732B2 (https=) |
| KR (1) | KR101156777B1 (https=) |
| AT (1) | ATE519795T1 (https=) |
| WO (1) | WO2005113622A1 (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10889662B2 (en) | 2014-12-12 | 2021-01-12 | Lg Chem, Ltd. | Metallocene-supported catalyst and method of preparing polyolefin using the same |
Families Citing this family (101)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7919561B2 (en) * | 1996-09-04 | 2011-04-05 | Exxonmobil Chemical Patents Inc. | Process of producing thermoplastic polymer blends |
| JP4748908B2 (ja) * | 1999-09-10 | 2011-08-17 | ザ・ユニバーシティ・オブ・シドニー | ジペプチジルペプチダーゼ |
| US8003725B2 (en) | 2002-08-12 | 2011-08-23 | Exxonmobil Chemical Patents Inc. | Plasticized hetero-phase polyolefin blends |
| US7271209B2 (en) | 2002-08-12 | 2007-09-18 | Exxonmobil Chemical Patents Inc. | Fibers and nonwovens from plasticized polyolefin compositions |
| CN100345896C (zh) | 2002-08-12 | 2007-10-31 | 埃克森美孚化学专利公司 | 增塑聚烯烃组合物 |
| US7531594B2 (en) | 2002-08-12 | 2009-05-12 | Exxonmobil Chemical Patents Inc. | Articles from plasticized polyolefin compositions |
| US7998579B2 (en) | 2002-08-12 | 2011-08-16 | Exxonmobil Chemical Patents Inc. | Polypropylene based fibers and nonwovens |
| US8653169B2 (en) * | 2002-10-15 | 2014-02-18 | Exxonmobil Chemical Patents Inc. | Propylene copolymers for adhesive applications |
| US7550528B2 (en) | 2002-10-15 | 2009-06-23 | Exxonmobil Chemical Patents Inc. | Functionalized olefin polymers |
| WO2004046214A2 (en) | 2002-10-15 | 2004-06-03 | Exxonmobil Chemical Patents Inc. | Multiple catalyst system for olefin polymerization and polymers produced therefrom |
| US7700707B2 (en) * | 2002-10-15 | 2010-04-20 | Exxonmobil Chemical Patents Inc. | Polyolefin adhesive compositions and articles made therefrom |
| US8618219B2 (en) | 2002-10-15 | 2013-12-31 | Exxonmobil Chemical Patents Inc. | Propylene copolymers for adhesive applications |
| US7541402B2 (en) | 2002-10-15 | 2009-06-02 | Exxonmobil Chemical Patents Inc. | Blend functionalized polyolefin adhesive |
| US8192813B2 (en) | 2003-08-12 | 2012-06-05 | Exxonmobil Chemical Patents, Inc. | Crosslinked polyethylene articles and processes to produce same |
| US7645829B2 (en) * | 2004-04-15 | 2010-01-12 | Exxonmobil Chemical Patents Inc. | Plasticized functionalized propylene copolymer adhesive composition |
| US8389615B2 (en) | 2004-12-17 | 2013-03-05 | Exxonmobil Chemical Patents Inc. | Elastomeric compositions comprising vinylaromatic block copolymer, polypropylene, plastomer, and low molecular weight polyolefin |
| AU2005319179B2 (en) * | 2004-12-21 | 2011-10-13 | Dow Global Technologies Llc | Polypropylene-based adhesive compositions |
| JP2008528779A (ja) | 2005-02-03 | 2008-07-31 | バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ | 射出成形用プロピレンポリマー組成物 |
| US8513366B2 (en) * | 2005-03-17 | 2013-08-20 | University Of Maryland, College Park | Methods for modulated degenerative transfer living polymerization and isotactic-atactic stereoblock and stereogradient poly(olefins) thereby |
| DE602006007572D1 (de) † | 2005-05-12 | 2009-08-13 | Basell Poliolefine Srl | Propylen-ethylen-copolymere und herstellungsverfahren dafür |
| US9745461B2 (en) | 2005-06-22 | 2017-08-29 | Exxonmobil Chemical Patents Inc. | Vulcanized polymer blends |
| US7928164B2 (en) * | 2005-06-22 | 2011-04-19 | Exxonmobil Chemical Patents Inc. | Homogeneous polymer blend and process of making the same |
| US7951872B2 (en) | 2005-06-22 | 2011-05-31 | Exxonmobil Chemical Patents Inc. | Heterogeneous polymer blend with continuous elastomeric phase and process of making the same |
| US20060293462A1 (en) * | 2005-06-22 | 2006-12-28 | Sunny Jacob | Heterogeneous polymer blend and process of making the same |
| US8022142B2 (en) * | 2008-12-15 | 2011-09-20 | Exxonmobil Chemical Patents Inc. | Thermoplastic olefin compositions |
| US9644092B2 (en) | 2005-06-22 | 2017-05-09 | Exxonmobil Chemical Patents Inc. | Heterogeneous in-situ polymer blend |
| WO2007001694A1 (en) * | 2005-06-24 | 2007-01-04 | Exxonmobil Chemical Patents Inc. | Functionalized propylene copolymer adheside composition |
| EP1899415B1 (en) | 2005-07-01 | 2011-08-10 | Basell Poliolefine Italia S.r.l. | Propylene polymers having broad molecular weight distribution |
| WO2007011530A2 (en) | 2005-07-15 | 2007-01-25 | Exxonmobil Chemical Patents, Inc. | Elastomeric compositions |
| US8748361B2 (en) | 2005-07-19 | 2014-06-10 | Exxonmobil Chemical Patents Inc. | Polyalpha-olefin compositions and processes to produce the same |
| US7989670B2 (en) * | 2005-07-19 | 2011-08-02 | Exxonmobil Chemical Patents Inc. | Process to produce high viscosity fluids |
| WO2007011462A1 (en) | 2005-07-19 | 2007-01-25 | Exxonmobil Chemical Patents Inc. | Lubricants from mixed alpha-olefin feeds |
| US8535514B2 (en) | 2006-06-06 | 2013-09-17 | Exxonmobil Research And Engineering Company | High viscosity metallocene catalyst PAO novel base stock lubricant blends |
| US8921290B2 (en) | 2006-06-06 | 2014-12-30 | Exxonmobil Research And Engineering Company | Gear oil compositions |
| US8299007B2 (en) | 2006-06-06 | 2012-10-30 | Exxonmobil Research And Engineering Company | Base stock lubricant blends |
| US8834705B2 (en) | 2006-06-06 | 2014-09-16 | Exxonmobil Research And Engineering Company | Gear oil compositions |
| US8501675B2 (en) | 2006-06-06 | 2013-08-06 | Exxonmobil Research And Engineering Company | High viscosity novel base stock lubricant viscosity blends |
| JP5555490B2 (ja) | 2006-07-19 | 2014-07-23 | エクソンモービル・ケミカル・パテンツ・インク | メタロセン触媒を用いたポリオレフィンの製造方法 |
| USD553444S1 (en) | 2006-08-22 | 2007-10-23 | Dart Industries Inc. | Seal for a food container |
| US20080073366A1 (en) * | 2006-08-22 | 2008-03-27 | Backaert Dimitri M C J | Fast freeze container and seal |
| USD559042S1 (en) | 2006-08-22 | 2008-01-08 | Dart Industries Inc. | Food container |
| CN101274968B (zh) * | 2007-03-28 | 2012-11-21 | 中国石油化工股份有限公司 | 一种用于生产宽分子量分布的聚乙烯的复合催化剂 |
| US8513478B2 (en) * | 2007-08-01 | 2013-08-20 | Exxonmobil Chemical Patents Inc. | Process to produce polyalphaolefins |
| TW200932770A (en) * | 2007-10-22 | 2009-08-01 | Univation Tech Llc | Metallocene catalysts and their use in polymerization processes |
| WO2009059007A2 (en) * | 2007-10-31 | 2009-05-07 | Lord Corporation | Additives for improved adhesion to oily substrates |
| US8143353B2 (en) * | 2008-01-18 | 2012-03-27 | Exxonmobil Chemical Patents Inc. | Polymerization process and adhesives therefrom |
| WO2009097069A1 (en) * | 2008-01-31 | 2009-08-06 | Exxonmobil Chemical Patents Inc. | Improved utilization of linear alpha olefins in the production of metallocene catalyzed poly-alpha olefins |
| US8865959B2 (en) | 2008-03-18 | 2014-10-21 | Exxonmobil Chemical Patents Inc. | Process for synthetic lubricant production |
| CN101977944A (zh) | 2008-03-31 | 2011-02-16 | 埃克森美孚化学专利公司 | 剪切稳定的高粘度pao的制备 |
| US8431642B2 (en) * | 2008-06-09 | 2013-04-30 | Exxonmobil Chemical Patents Inc. | Polyolefin adhesive compositions and articles made therefrom |
| US8242198B2 (en) | 2008-06-09 | 2012-08-14 | Exxonmobil Chemical Patents Inc. | Polyolefin adhesive compositions |
| US8283400B2 (en) * | 2008-06-09 | 2012-10-09 | Exxonmobil Chemical Patents Inc. | Polyolefin adhesive compositions |
| US8372930B2 (en) | 2008-06-20 | 2013-02-12 | Exxonmobil Chemical Patents Inc. | High vinyl terminated propylene based oligomers |
| US8283428B2 (en) * | 2008-06-20 | 2012-10-09 | Exxonmobil Chemical Patents Inc. | Polymacromonomer and process for production thereof |
| US8802797B2 (en) | 2008-06-20 | 2014-08-12 | Exxonmobil Chemical Patents Inc. | Vinyl-terminated macromonomer oligomerization |
| US8283419B2 (en) * | 2008-06-20 | 2012-10-09 | Exxonmobil Chemical Patents Inc. | Olefin functionalization by metathesis reaction |
| US8399725B2 (en) * | 2008-06-20 | 2013-03-19 | Exxonmobil Chemical Patents Inc. | Functionalized high vinyl terminated propylene based oligomers |
| US8394746B2 (en) | 2008-08-22 | 2013-03-12 | Exxonmobil Research And Engineering Company | Low sulfur and low metal additive formulations for high performance industrial oils |
| US8247358B2 (en) | 2008-10-03 | 2012-08-21 | Exxonmobil Research And Engineering Company | HVI-PAO bi-modal lubricant compositions |
| ES2655738T3 (es) * | 2008-11-19 | 2018-02-21 | Exxonmobil Chemical Patents Inc. | Composiciones adhesivas y métodos para su fabricación |
| US8093335B2 (en) * | 2008-12-15 | 2012-01-10 | Exxonmobil Chemical Patents Inc. | Thermoplastic polyolefin in-reactor blends and molded articles therefrom |
| US8106127B2 (en) * | 2008-12-15 | 2012-01-31 | Exxonmobil Chemical Patents Inc. | Heterogeneous in-reactor polymer blends |
| EP2435526A4 (en) * | 2009-05-29 | 2012-10-31 | Exxonmobil Chem Patents Inc | POLYOLEFINIC ADHESIVE COMPOSITIONS AND PROCESS FOR PRODUCING THE SAME |
| US20100316820A1 (en) * | 2009-06-16 | 2010-12-16 | Rainer Kolb | Composite Materials Comprising Propylene-Based Polymer Blend Coatings |
| US20110059277A1 (en) * | 2009-09-04 | 2011-03-10 | Rainer Kolb | Elastomeric Surface Coatings for Plastic Articles |
| WO2010147706A2 (en) * | 2009-06-16 | 2010-12-23 | Exxonmobil Chemical Patents Inc. | Polyolefin compositions for coating applications |
| US20110054117A1 (en) * | 2009-08-27 | 2011-03-03 | Hall Gregory K | Polyolefin Adhesive Compositions and Method of Making Thereof |
| JP2011099091A (ja) | 2009-09-30 | 2011-05-19 | Sumitomo Chemical Co Ltd | エチレン系重合体の製造方法 |
| US8716201B2 (en) | 2009-10-02 | 2014-05-06 | Exxonmobil Research And Engineering Company | Alkylated naphtylene base stock lubricant formulations |
| CN102666806B (zh) | 2009-12-24 | 2015-09-16 | 埃克森美孚化学专利公司 | 用于生产新型合成基础油料的方法 |
| US9416206B2 (en) | 2010-01-22 | 2016-08-16 | Exxonmobil Chemical Patents Inc. | Lubricating oil compositions and method for making them |
| US8642523B2 (en) | 2010-02-01 | 2014-02-04 | Exxonmobil Research And Engineering Company | Method for improving the fuel efficiency of engine oil compositions for large low and medium speed engines by reducing the traction coefficient |
| US8748362B2 (en) | 2010-02-01 | 2014-06-10 | Exxonmobile Research And Engineering Company | Method for improving the fuel efficiency of engine oil compositions for large low and medium speed gas engines by reducing the traction coefficient |
| US8598103B2 (en) | 2010-02-01 | 2013-12-03 | Exxonmobil Research And Engineering Company | Method for improving the fuel efficiency of engine oil compositions for large low, medium and high speed engines by reducing the traction coefficient |
| US8728999B2 (en) | 2010-02-01 | 2014-05-20 | Exxonmobil Research And Engineering Company | Method for improving the fuel efficiency of engine oil compositions for large low and medium speed engines by reducing the traction coefficient |
| US8759267B2 (en) | 2010-02-01 | 2014-06-24 | Exxonmobil Research And Engineering Company | Method for improving the fuel efficiency of engine oil compositions for large low and medium speed engines by reducing the traction coefficient |
| CN102234188B (zh) * | 2010-05-06 | 2013-08-14 | 同济大学 | 一种环保型温拌沥青混合料的制备方法 |
| US8278403B2 (en) | 2010-07-08 | 2012-10-02 | Fina Technology, Inc. | Multi-component catalyst systems and polymerization processes for forming broad composition distribution polymers |
| US9815915B2 (en) | 2010-09-03 | 2017-11-14 | Exxonmobil Chemical Patents Inc. | Production of liquid polyolefins |
| WO2012176946A1 (ko) * | 2011-06-24 | 2012-12-27 | Sk 이노베이션 주식회사 | 공중합성이 우수한 전이금속 촉매계 및 이를 이용한 에틸렌 단독중합체 또는 에틸렌과 α-올레핀의 공중합체 제조방법 |
| US9234151B2 (en) | 2011-10-10 | 2016-01-12 | Exxonmobil Research And Engineering Company | Lubricating compositions |
| CA2856196C (en) | 2011-12-06 | 2020-09-01 | Masco Corporation Of Indiana | Ozone distribution in a faucet |
| CN102964963B (zh) * | 2012-11-05 | 2015-03-04 | 江门四方威凯精细化工有限公司 | 一种换热器用防腐蚀导热涂料及其制备方法 |
| US9422385B2 (en) | 2013-01-30 | 2016-08-23 | Exxonmobil Chemical Patents Inc. | Polyethylene copolymers with vinyl terminated macromonomers as comonomers |
| US9376559B2 (en) * | 2013-11-22 | 2016-06-28 | Exxonmobil Chemical Patents Inc. | Reverse staged impact copolymers |
| US9382361B2 (en) | 2014-03-21 | 2016-07-05 | Exxonmobil Chemical Patents Inc. | Process to produce ethylene propylene copolymers |
| EP2995631A1 (en) | 2014-09-12 | 2016-03-16 | Borealis AG | Process for producing graft copolymers on polyolefin backbone |
| CN104559166B (zh) * | 2014-12-18 | 2016-08-17 | 成都新柯力化工科技有限公司 | 一种石头纸专用高分子材料及其制备方法 |
| SG11201705239SA (en) | 2014-12-29 | 2017-07-28 | Dow Global Technologies Llc | Process to form ethylene/alpha-olefin interpolymers |
| WO2016114915A1 (en) | 2015-01-14 | 2016-07-21 | Exxonmobil Chemical Patents Inc. | Polymer compositions and processes for their production |
| JP6654234B2 (ja) * | 2015-08-25 | 2020-02-26 | エクソンモービル・ケミカル・パテンツ・インク | その場で油生成を伴うエチレンコポリマー |
| WO2017112795A1 (en) | 2015-12-21 | 2017-06-29 | Delta Faucet Company | Fluid delivery system including a disinfectant device |
| EP3260512B1 (en) | 2016-06-20 | 2021-02-24 | Henkel AG & Co. KGaA | Extrudable pressure sensitive adhesive based on polybutene-1 suitable for reclosable packagings |
| PT3323866T (pt) | 2016-11-22 | 2019-08-21 | Henkel Ag & Co Kgaa | Adesivo extrudável sensível a pressão, à base de polímero de polibuteno-1 e um copolímero de estireno, adequado para embalagens refecháveis |
| US11193008B2 (en) | 2017-04-10 | 2021-12-07 | Exxonmobil Chemical Patents Inc. | Methods for making polyolefin polymer compositions |
| US10131680B1 (en) | 2017-06-14 | 2018-11-20 | Up Chemical Co., Ltd. | Group 4 metal element-containing alkoxy compound, preparing method thereof, precursor composition including the same for film deposition, and method of depositing film using the same |
| KR101788558B1 (ko) | 2017-06-14 | 2017-10-23 | 주식회사 유피케미칼 | 4 족 금속 원소-함유 알콕시 화합물, 이의 제조 방법, 이를 포함하는 막 증착용 전구체 조성물, 및 이를 이용하는 막의 증착 방법 |
| KR102153474B1 (ko) | 2017-06-20 | 2020-09-08 | 주식회사 엘지화학 | 에틸렌 비닐아세테이트 공중합 공정 제어 시스템 및 그 제어 방법 |
| US10683376B2 (en) | 2017-11-07 | 2020-06-16 | Nova Chemicals (International) S.A. | Manufacturing ethylene interpolymer products at higher production rate |
| US10995166B2 (en) | 2017-11-07 | 2021-05-04 | Nova Chemicals (International) S.A. | Ethylene interpolymer products and films |
| CN117897414A (zh) * | 2021-09-23 | 2024-04-16 | 博里利斯股份公司 | 用于生产丙烯共聚物的方法 |
Family Cites Families (657)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1953104A (en) * | 1930-01-27 | 1934-04-03 | Du Pont Cellophane Co Inc | Adhesive |
| US5066737A (en) | 1990-10-22 | 1991-11-19 | Shell Oil Company | Olefin polymerization catalyst |
| US3248179A (en) | 1962-02-26 | 1966-04-26 | Phillips Petroleum Co | Method and apparatus for the production of solid polymers of olefins |
| GB1003632A (en) | 1963-05-02 | 1965-09-08 | Oxford Paper Co | Improvements in planograpic printing plates |
| US3221002A (en) | 1963-09-26 | 1965-11-30 | Cabot Corp | Process for polymerization utilizing a surface treated inorganic solid catalyst |
| US3242099A (en) | 1964-03-27 | 1966-03-22 | Union Carbide Corp | Olefin polymerization catalysts |
| US3231550A (en) | 1964-06-04 | 1966-01-25 | Union Carbide Corp | Olefin polymerization |
| FR1582841A (https=) | 1967-03-29 | 1969-10-10 | ||
| US3487112A (en) | 1967-04-27 | 1969-12-30 | Monsanto Co | Vapor phase hydroformylation process |
| US3709954A (en) | 1970-03-16 | 1973-01-09 | Union Carbide Corp | Preparation of liquid polymers of olefins |
| US3709853A (en) | 1971-04-29 | 1973-01-09 | Union Carbide Corp | Polymerization of ethylene using supported bis-(cyclopentadienyl)chromium(ii)catalysts |
| US4115639A (en) | 1971-06-24 | 1978-09-19 | Union Carbide Corporation | Ethylene polymerization with ether modified catalyst |
| US3868433A (en) | 1972-04-03 | 1975-02-25 | Exxon Research Engineering Co | Thermoplastic adhesive compositions |
| US3821143A (en) * | 1973-03-22 | 1974-06-28 | Du Pont | Hot melt adhesive composition containing a branched elastomeric copolymer |
| IT1037112B (it) | 1975-03-28 | 1979-11-10 | Montedison Spa | Catalizzatori per la polimerizzazione delle olfine |
| US3954697A (en) * | 1975-03-31 | 1976-05-04 | Eastman Kodak Company | Poly(higher-1-olefin-co-propylene) copolymers as hot-melt, pressure-sensitive adhesives |
| US4217428A (en) | 1975-03-31 | 1980-08-12 | Eastman Kodak Company | Blends of substantially amorphous higher 1-olefin copolymers and tackifying resins useful as pressure-sensitive adhesives |
| GB1538057A (en) | 1975-08-13 | 1979-01-10 | Exxon Research Engineering Co | Petroleum resins |
| US4077904A (en) | 1976-06-29 | 1978-03-07 | Union Carbide Corporation | Olefin polymerization process and catalyst therefor |
| DE2742585A1 (de) | 1976-09-28 | 1978-03-30 | Asahi Chemical Ind | Neue polymerisationskatalysatoren und ihre verwendung (i) |
| JPS5952643B2 (ja) * | 1977-01-27 | 1984-12-20 | 三井化学株式会社 | エチレン共重合体 |
| US4178272A (en) | 1977-03-02 | 1979-12-11 | Eastman Kodak Company | Hot-melt adhesvies for bonding polyethylene |
| DE2731067C3 (de) | 1977-07-09 | 1981-11-26 | Bunawerke Hüls GmbH, 4370 Marl | Verfahren zur Herstellung von Polybutadien mit einem hohen Gehalt an Monomereneinheiten in cis-1,4- Struktur |
| US4302566A (en) | 1978-03-31 | 1981-11-24 | Union Carbide Corporation | Preparation of ethylene copolymers in fluid bed reactor |
| US4302565A (en) | 1978-03-31 | 1981-11-24 | Union Carbide Corporation | Impregnated polymerization catalyst, process for preparing, and use for ethylene copolymerization |
| US4482687A (en) | 1979-10-26 | 1984-11-13 | Union Carbide Corporation | Preparation of low-density ethylene copolymers in fluid bed reactor |
| US4376062A (en) | 1979-11-28 | 1983-03-08 | Union Carbide Corporation | Spheroidal polymerization catalyst, process for preparing, and use for ethylene polymerization |
| US4325837A (en) | 1980-08-12 | 1982-04-20 | Phillips Petroleum Company | Catalyst, method of producing the catalyst, and polymerization process employing the catalyst |
| EP0046344B1 (en) | 1980-08-19 | 1985-06-19 | Imperial Chemical Industries Plc | Fermentation process |
| US4379758A (en) | 1980-12-24 | 1983-04-12 | Union Carbide Corporation | Catalyst composition for polymerizing ethylene |
| DE3127133A1 (de) | 1981-07-09 | 1983-01-27 | Hoechst Ag, 6000 Frankfurt | Verfahren zur herstellung von polyolefinen und deren copolymerisaten |
| CA1174800A (en) | 1981-08-24 | 1984-09-18 | Charles Cozewith | Gas phase method for producing copolymers of ethylene and higher alpha-olefins |
| JPS5883016A (ja) | 1981-11-13 | 1983-05-18 | Mitsui Petrochem Ind Ltd | プロピレンブロツク共重合体の製法 |
| ES8405434A1 (es) | 1981-12-21 | 1984-06-01 | Exxon Research Engineering Co | Un procedimiento para la hidrogenacion de resinas de petroleo. |
| CA1219994A (en) | 1981-12-24 | 1987-03-31 | Nobunori Maehara | Process for producing polybutadiene rubber with enhanced mechanical strength |
| US4588790A (en) | 1982-03-24 | 1986-05-13 | Union Carbide Corporation | Method for fluidized bed polymerization |
| US4543399A (en) | 1982-03-24 | 1985-09-24 | Union Carbide Corporation | Fluidized bed reaction systems |
| DE3366573D1 (en) | 1982-06-24 | 1986-11-06 | Bp Chimie Sa | Process for the polymerization and copolymerization of alpha-olefins in a fluidized bed |
| US4496698A (en) * | 1982-07-26 | 1985-01-29 | The Dow Chemical Company | Process for producing polyethylene having constant physical and chemical properties |
| JPS5975910A (ja) * | 1982-10-25 | 1984-04-28 | Mitsui Petrochem Ind Ltd | エチレン共重合体 |
| DE3240383A1 (de) | 1982-11-02 | 1984-05-03 | Hoechst Ag, 6230 Frankfurt | Verfahren zur herstellung von oligomeren aluminoxanen |
| JPS59117508A (ja) * | 1982-12-24 | 1984-07-06 | Mitsui Petrochem Ind Ltd | エチレンの重合法 |
| EP0115940B2 (en) * | 1983-01-25 | 1997-03-19 | Mitsui Petrochemical Industries, Ltd. | Film-forming propylene copolymer, film thereof and process for production of the film |
| EP0115434A3 (en) | 1983-01-27 | 1984-08-29 | Exxon Research And Engineering Company | Semicrystalline ethylene alpha-olefin copolymers for hot melt adhesives |
| US4935474A (en) * | 1983-06-06 | 1990-06-19 | Exxon Research & Engineering Company | Process and catalyst for producing polyethylene having a broad molecular weight distribution |
| ZA844157B (en) | 1983-06-06 | 1986-01-29 | Exxon Research Engineering Co | Process and catalyst for polyolefin density and molecular weight control |
| US5324800A (en) | 1983-06-06 | 1994-06-28 | Exxon Chemical Patents Inc. | Process and catalyst for polyolefin density and molecular weight control |
| US4937299A (en) * | 1983-06-06 | 1990-06-26 | Exxon Research & Engineering Company | Process and catalyst for producing reactor blend polyolefins |
| US4882406A (en) | 1983-06-15 | 1989-11-21 | Exxon Research & Engineering Company | Nodular copolymers formed of alpha-olefin copolymers coupled by non-conjugated dienes |
| GB8317510D0 (en) | 1983-06-28 | 1983-08-03 | Exxon Research Engineering Co | Petroleum resins |
| JPS6088016A (ja) * | 1983-10-21 | 1985-05-17 | Mitsui Petrochem Ind Ltd | エチレン共重合体 |
| FR2555182B1 (fr) | 1983-11-23 | 1986-11-07 | Bp Chimie Sa | Procede de preparation de catalyseur supporte pour la copolymerisation de l'ethylene avec des alpha-olefines superieures |
| JPS60166455A (ja) * | 1983-12-29 | 1985-08-29 | 住友化学工業株式会社 | ポリプロピレン積層フイルム |
| US4613484A (en) | 1984-11-30 | 1986-09-23 | Phillips Petroleum Company | Loop reactor settling leg system for separation of solid polymers and liquid diluent |
| JPS61192240A (ja) | 1985-02-20 | 1986-08-26 | 株式会社 オシキリ | パン生地温度制御方法および装置 |
| US5231126A (en) | 1985-04-01 | 1993-07-27 | Shi Guan Yi | Beta-crystalline form of isotactic polypropylene and method for forming the same |
| US4897455A (en) | 1985-06-21 | 1990-01-30 | Exxon Chemical Patents Inc. | Polymerization process |
| CA1268753A (en) | 1985-06-21 | 1990-05-08 | Exxon Chemical Patents, Inc. | Supported polymerization catalyst |
| US4808561A (en) | 1985-06-21 | 1989-02-28 | Exxon Chemical Patents Inc. | Supported polymerization catalyst |
| US4665208A (en) | 1985-07-11 | 1987-05-12 | Exxon Chemical Patents Inc. | Process for the preparation of alumoxanes |
| US4668834B1 (en) * | 1985-10-16 | 1996-05-07 | Uniroyal Chem Co Inc | Low molecular weight ethylene-alphaolefin copolymer intermediates |
| US4701432A (en) | 1985-11-15 | 1987-10-20 | Exxon Chemical Patents Inc. | Supported polymerization catalyst |
| US5124418A (en) | 1985-11-15 | 1992-06-23 | Exxon Chemical Patents Inc. | Supported polymerization catalyst |
| FR2599826B1 (fr) | 1986-06-04 | 1989-08-25 | Fives Cail Babcock | Procede de regulation d'une installation de fabrication du ciment en voie seche avec precalcination |
| US4689437A (en) | 1986-07-21 | 1987-08-25 | Union Carbide Corporation | Oligomerization to alpha-olefins |
| US5077255A (en) | 1986-09-09 | 1991-12-31 | Exxon Chemical Patents Inc. | New supported polymerization catalyst |
| EP0812862B1 (en) | 1986-09-24 | 2002-11-13 | Mitsui Chemicals, Inc. | Process for polymerizing olefins |
| KR920000173B1 (ko) | 1986-10-09 | 1992-01-09 | 미쓰이세끼유 가가꾸고오교오 가부시끼가이샤 | 저결정성 프로필렌계 랜덤 공중합체 조성물, 그 제조방법 및 폴리프로필렌 복합 적층체 |
| JPH0780933B2 (ja) | 1986-11-20 | 1995-08-30 | 三井石油化学工業株式会社 | オレフインの重合方法 |
| DE3640924A1 (de) | 1986-11-29 | 1988-06-01 | Hoechst Ag | 1-olefin-stereoblockpolymer und verfahren zu seiner herstellung |
| FR2609036B1 (fr) | 1986-12-29 | 1989-04-14 | Bp Chimie Sa | Polymerisation ou copolymerisation d'ethylene en phase gazeuse en presence d'un prepolymere comprenant un catalyseur d'oxyde de chrome |
| US5384299A (en) | 1987-01-30 | 1995-01-24 | Exxon Chemical Patents Inc. | Ionic metallocene catalyst compositions |
| US5055438A (en) | 1989-09-13 | 1991-10-08 | Exxon Chemical Patents, Inc. | Olefin polymerization catalysts |
| US5198401A (en) | 1987-01-30 | 1993-03-30 | Exxon Chemical Patents Inc. | Ionic metallocene catalyst compositions |
| US5264405A (en) | 1989-09-13 | 1993-11-23 | Exxon Chemical Patents Inc. | Monocyclopentadienyl titanium metal compounds for ethylene-α-olefin-copolymer production catalysts |
| IL85097A (en) | 1987-01-30 | 1992-02-16 | Exxon Chemical Patents Inc | Catalysts based on derivatives of a bis(cyclopentadienyl)group ivb metal compound,their preparation and their use in polymerization processes |
| PL276385A1 (en) | 1987-01-30 | 1989-07-24 | Exxon Chemical Patents Inc | Method for polymerization of olefines,diolefins and acetylene unsaturated compounds |
| US5153157A (en) | 1987-01-30 | 1992-10-06 | Exxon Chemical Patents Inc. | Catalyst system of enhanced productivity |
| US5241025A (en) | 1987-01-30 | 1993-08-31 | Exxon Chemical Patents Inc. | Catalyst system of enhanced productivity |
| JPH0742301B2 (ja) | 1987-02-14 | 1995-05-10 | 三井石油化学工業株式会社 | 微粒子状アルミノオキサン、その製法およびその用途 |
| US5003019A (en) * | 1987-03-02 | 1991-03-26 | Mitsui Petrochemical Industries, Ltd. | Cyclo-olefinic random copolymer, olefinic random copolymer, and process for producing cyclo-olefinic random copolymers |
| EP0284708B1 (en) | 1987-04-03 | 1996-01-31 | Fina Technology, Inc. | Metallocene catalyst systems for olefin polymerization having a silicon hydrocarbyl bridge. |
| JP2538588B2 (ja) | 1987-04-03 | 1996-09-25 | 三井石油化学工業株式会社 | オレフイン重合用固体触媒の製法 |
| US4939217A (en) | 1987-04-03 | 1990-07-03 | Phillips Petroleum Company | Process for producing polyolefins and polyolefin catalysts |
| US4794096A (en) | 1987-04-03 | 1988-12-27 | Fina Technology, Inc. | Hafnium metallocene catalyst for the polymerization of olefins |
| US5206199A (en) | 1987-04-20 | 1993-04-27 | Mitsui Petrochemical Industries, Ltd. | Catalyst for polymerizing an olefin and process for polymerizing an olefin |
| US5093415A (en) | 1987-05-19 | 1992-03-03 | Union Carbide Chemicals & Plastics Technology Corporation | Process for producing stereoregular polymers having a narrow molecular weight distribution |
| DE3726067A1 (de) | 1987-08-06 | 1989-02-16 | Hoechst Ag | Verfahren zur herstellung von 1-olefinpolymeren |
| US5015749A (en) | 1987-08-31 | 1991-05-14 | The Dow Chemical Company | Preparation of polyhydrocarbyl-aluminoxanes |
| ES2064322T3 (es) | 1987-09-11 | 1995-02-01 | Fina Technology | Sistemas de catalisis para la produccion de poliolefinas cubriendo una gama amplia de pesos moleculares. |
| US4975403A (en) | 1987-09-11 | 1990-12-04 | Fina Technology, Inc. | Catalyst systems for producing polyolefins having a broad molecular weight distribution |
| US5021257A (en) | 1987-11-30 | 1991-06-04 | Eastman Kodak Company | Hot-melt adhesive composition |
| EP0319043A3 (en) | 1987-12-04 | 1991-03-20 | Union Carbide Corporation | Hot melt adhesives |
| FR2628110B1 (fr) | 1988-03-03 | 1994-03-25 | Bp Chimie | Catalyseur de polymerisation d'olefines de type ziegler-natta, supporte sur des particules spheriques de chlorure de magnesium, et procede de preparation |
| US5017714A (en) | 1988-03-21 | 1991-05-21 | Exxon Chemical Patents Inc. | Silicon-bridged transition metal compounds |
| US5120867A (en) | 1988-03-21 | 1992-06-09 | Welborn Jr Howard C | Silicon-bridged transition metal compounds |
| FR2629450B1 (fr) | 1988-04-01 | 1992-04-30 | Rhone Poulenc Chimie | Materiaux supraconducteurs stabilises et leur procede d'obtention |
| US5149819A (en) | 1988-04-28 | 1992-09-22 | Ricoh Company, Ltd. | Squarylium compounds and optical information recording medium using the same |
| US4950720A (en) | 1988-04-29 | 1990-08-21 | Exxon Chemical Patents Inc. | Modified polypropylene, process for making and article made from the same |
| US5039614A (en) | 1988-06-16 | 1991-08-13 | Armenag Dekmezian | Method and apparatus for collecting samples for analysis of chemical composition |
| 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 |
| CA1319539C (en) | 1988-06-16 | 1993-06-29 | Armenag H. Dekmezian | Method and apparatus for collecting samples for analysis of chemical composition |
| FI893348A7 (fi) * | 1988-07-11 | 1990-01-12 | Sumitomo Chemical Co | Etyleeni- -olefiinikopolymeeri ja siitä valmistettuja kalvoja |
| US4892851A (en) * | 1988-07-15 | 1990-01-09 | Fina Technology, Inc. | Process and catalyst for producing syndiotactic polyolefins |
| US5155080A (en) | 1988-07-15 | 1992-10-13 | Fina Technology, Inc. | Process and catalyst for producing syndiotactic polyolefins |
| FR2634212B1 (fr) | 1988-07-15 | 1991-04-19 | Bp Chimie Sa | Appareillage et procede de polymerisation d'olefines en phase gazeuse dans un reacteur a lit fluidise |
| US5225500A (en) | 1988-07-15 | 1993-07-06 | Fina Technology, Inc. | Process and catalyst for producing syndiotactic polyolefins |
| DE3826075A1 (de) | 1988-07-30 | 1990-02-01 | Hoechst Ag | 1-olefin-isoblockpolymer und verfahren zu seiner herstellung |
| JP2600829B2 (ja) | 1988-08-04 | 1997-04-16 | 三井石油化学工業株式会社 | ポリプロピレン樹脂組成物 |
| US5091352A (en) | 1988-09-14 | 1992-02-25 | Mitsui Petrochemical Industries, Ltd. | Olefin polymerization catalyst component, olefin polymerization catalyst and process for the polymerization of olefins |
| KR920006464B1 (ko) | 1988-09-14 | 1992-08-07 | 미쓰이 세끼유 가가꾸 고오교오 가부시끼가이샤 | 올레핀중합용 촉매성분, 올레핀중합용 촉매 및 이 올레핀중합용 촉매를 사용한 올레핀의 중합방법 |
| EP0366411A3 (en) | 1988-10-28 | 1991-04-24 | Exxon Chemical Patents Inc. | Graft polymers of ethylene-propylene-diene monomer polymers with propylene, means of preparation, and use of polypropylene compositions |
| US5041584A (en) | 1988-12-02 | 1991-08-20 | Texas Alkyls, Inc. | Modified methylaluminoxane |
| US4908463A (en) | 1988-12-05 | 1990-03-13 | Ethyl Corporation | Aluminoxane process |
| US5218071A (en) | 1988-12-26 | 1993-06-08 | Mitsui Petrochemical Industries, Ltd. | Ethylene random copolymers |
| US5639842A (en) * | 1988-12-26 | 1997-06-17 | Mitsui Petrochemical Industries, Ltd. | Ethylene random copolymers |
| EP0955322A3 (en) | 1988-12-26 | 1999-12-08 | Mitsui Chemicals, Inc. | Olefin copolymers and processes for preparing same |
| US5103031A (en) | 1989-02-21 | 1992-04-07 | Ethyl Corporation | Falling film aluminoxane process |
| DE3907964A1 (de) | 1989-03-11 | 1990-09-13 | Hoechst Ag | Verfahren zur herstellung eines syndiotaktischen polyolefins |
| DE3916555A1 (de) | 1989-05-20 | 1990-11-22 | Hoechst Ag | Verfahren zur herstellung von ethylenpolymeren |
| US4968827A (en) | 1989-06-06 | 1990-11-06 | Ethyl Corporation | Alkylaluminoxane process |
| JP2818199B2 (ja) | 1989-06-12 | 1998-10-30 | 三井化学株式会社 | シンジオタクチックポリプロピレン樹脂組成物およびその製造方法 |
| US5594172A (en) * | 1989-06-21 | 1997-01-14 | Nissan Motor Co., Ltd. | Semiconductor accelerometer having a cantilevered beam with a triangular or pentagonal cross section |
| US4924018A (en) | 1989-06-26 | 1990-05-08 | Ethyl Corporation | Alkylaluminoxane process |
| US5376612A (en) | 1989-08-10 | 1994-12-27 | Phillips Petroleum Company | Chromium catalysts and process for making chromium catalysts |
| 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 |
| DE3930205A1 (de) | 1989-09-09 | 1991-03-14 | Borsig Babcock Ag | Rohrbuendel-waermetauscher |
| US5548014A (en) | 1989-09-13 | 1996-08-20 | Exxon Chemical Patents Inc. | Blends of ethylene copolymers for hot melt adhesives |
| DD300443A5 (de) * | 1989-09-13 | 1992-06-11 | Exxon Chemical Patents Inc | Heissschmelzklebstoff |
| US5504169A (en) | 1989-09-13 | 1996-04-02 | Exxon Chemical Patents Inc. | Process for producing amorphous poly-α-olefins with a monocyclopentadienyl transition metal catalyst system |
| US5227440A (en) | 1989-09-13 | 1993-07-13 | Exxon Chemical Patents Inc. | Mono-Cp heteroatom containing Group IVB transition metal complexes with MAO: supported catalysts for olefin polymerization |
| US5026798A (en) | 1989-09-13 | 1991-06-25 | Exxon Chemical Patents Inc. | Process for producing crystalline poly-α-olefins with a monocyclopentadienyl transition metal catalyst system |
| 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 |
| US5066741A (en) | 1990-03-22 | 1991-11-19 | The Dow Chemical Company | Process for preparation of syndiotactic vinyl aromatic polymers |
| US5763549A (en) | 1989-10-10 | 1998-06-09 | Fina Technology, Inc. | Cationic metallocene catalysts based on organoaluminum anions |
| DE69026907T2 (de) | 1989-10-10 | 1996-10-10 | Fina Technology | Metallocenkatalysator mit Lewissäure und Alkylaluminium |
| US5036034A (en) | 1989-10-10 | 1991-07-30 | Fina Technology, Inc. | Catalyst for producing hemiisotactic polypropylene |
| US5387568A (en) | 1989-10-30 | 1995-02-07 | Fina Technology, Inc. | Preparation of metallocene catalysts for polymerization of olefins |
| ATE120768T1 (de) | 1989-10-30 | 1995-04-15 | Fina Technology | Herstellung von metallocenkatalysatoren für olefinpolymerisation. |
| GB8925685D0 (en) | 1989-11-14 | 1990-01-04 | Exxon Chemical Patents Inc | Resin use for tackification |
| US5087809A (en) | 1990-11-26 | 1992-02-11 | Eastman Kodak Company | Spectrally selective dithering and color filter mask for increased image sensor blue sensitivity |
| IL96810A0 (en) | 1990-01-02 | 1991-09-16 | Exxon Chemical Patents Inc | Supported ionic metallocene catalysts for olefin polymerization and methods for the preparation thereof |
| US5519091A (en) * | 1990-02-13 | 1996-05-21 | Mitsui Petrochemical Industries, Ltd. | Method for the preparation of ethylene polymer compositions |
| TW206240B (https=) * | 1990-02-13 | 1993-05-21 | Mitsui Petroleum Chemicals Ind | |
| US5151474A (en) | 1990-02-16 | 1992-09-29 | The Dow Chemical Company | Process control method for manufacturing polyolefin |
| US5171793A (en) | 1990-02-22 | 1992-12-15 | Exxon Chemical Patents Inc. | Hydrogenated resins, adhesive formulations and process for production of resins |
| US5114897A (en) | 1990-04-18 | 1992-05-19 | The Dow Chemical Company | Catalyst and process for polymerizing olefins |
| 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 |
| DE4015254A1 (de) | 1990-05-12 | 1991-11-14 | Hoechst Ag | Verfahren zur herstellung eines polyolefins |
| US5326824A (en) | 1990-05-18 | 1994-07-05 | Mitsui Toatsu Chemicals, Incorporated | Syndiotactic propylene copolymer, method for preparing same, and its use |
| JP2927885B2 (ja) | 1990-05-24 | 1999-07-28 | 三井化学株式会社 | シンジオタクチックポリα―オレフィンの製造方法 |
| PL166690B1 (pl) | 1990-06-04 | 1995-06-30 | Exxon Chemical Patents Inc | Sposób wytwarzania polimerów olefin PL |
| US5041585A (en) | 1990-06-08 | 1991-08-20 | Texas Alkyls, Inc. | Preparation of aluminoxanes |
| RU2118203C1 (ru) | 1990-06-22 | 1998-08-27 | Экксон Кэмикал Пейтентс Инк. | Каталитическая система для получения полиолефинов и композиция, используемая для полимеризации олефинов |
| US5272236A (en) | 1991-10-15 | 1993-12-21 | The Dow Chemical Company | Elastic substantially linear olefin polymers |
| 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 |
| JP3115595B2 (ja) | 1990-07-24 | 2000-12-11 | 三井化学株式会社 | α―オレフィンの重合触媒及びそれを用いたポリ―α―オレフィンの製造方法 |
| US5145689A (en) | 1990-10-17 | 1992-09-08 | Exxon Chemical Patents Inc. | Meltblowing die |
| US5096743A (en) | 1990-11-09 | 1992-03-17 | E. I. Du Pont De Nemours And Company | Process for making roofing membrane of epdm elastomer and ethylene-containing polymer |
| US5317070A (en) * | 1990-11-09 | 1994-05-31 | Exxon Chemical Patents, Inc. | Syndiotactic hot melt adhesive |
| DE59107926D1 (de) | 1990-11-12 | 1996-07-18 | Hoechst Ag | Metallocene mit Liganden aus 2-substituierten Indenylderivaten, Verfahren zu ihrer Herstellung und ihre Verwendung als Katalysatoren |
| ES2071888T3 (es) | 1990-11-12 | 1995-07-01 | Hoechst Ag | Bisindenilmetalocenos sustituidos en posicion 2, procedimiento para su preparacion y su utilizacion como catalizadores en la polimerizacion de olefinas. |
| US5239022A (en) | 1990-11-12 | 1993-08-24 | Hoechst Aktiengesellschaft | Process for the preparation of a syndiotactic polyolefin |
| US5243001A (en) | 1990-11-12 | 1993-09-07 | Hoechst Aktiengesellschaft | Process for the preparation of a high molecular weight olefin polymer |
| JPH051185A (ja) | 1990-11-16 | 1993-01-08 | Mitsubishi Petrochem Co Ltd | 強度に優れた熱可塑性樹脂組成物及びその製造法 |
| EP0513380B2 (en) | 1990-11-30 | 2011-02-23 | Idemitsu Kosan Company Limited | Process for producing olefinic polymer |
| DE69117534T3 (de) | 1990-12-27 | 2002-10-10 | Exxon Mobil Chemical Patents Inc., Wilmington | Heissschmelzklebezusammensetzung |
| US5189192A (en) | 1991-01-16 | 1993-02-23 | The Dow Chemical Company | Process for preparing addition polymerization catalysts via metal center oxidation |
| US5206197A (en) | 1991-03-04 | 1993-04-27 | The Dow Chemical Company | Catalyst composition for preparation of syndiotactic vinyl aromatic polymers |
| CA2060019A1 (en) | 1991-03-04 | 1992-09-05 | Phil Marvin Stricklen | Process for producing polyolefins having a bimodal molecular weight distribution |
| JP3117231B2 (ja) | 1991-03-11 | 2000-12-11 | 三井化学株式会社 | 幅広い分子量分布を有するシンジオタクチックポリ−α−オレフィンの製造方法 |
| TW218884B (https=) | 1991-05-01 | 1994-01-11 | Mitsubishi Kakoki Kk | |
| US5436305A (en) | 1991-05-09 | 1995-07-25 | Phillips Petroleum Company | Organometallic fluorenyl compounds, preparation, and use |
| US5571880A (en) | 1991-05-09 | 1996-11-05 | Phillips Petroleum Company | Organometallic fluorenyl compounds and use thereof in an alpha-olefin polymerization process |
| CA2058383A1 (en) | 1991-05-17 | 1992-11-18 | Phillips Petroleum Company | Olefin polymerization |
| EP0515132B2 (en) | 1991-05-20 | 2003-08-27 | Mitsui Chemicals, Inc. | Olefin polymerization catalyst and olefin polymerization |
| EP0702030B1 (de) | 1991-05-27 | 2001-03-21 | TARGOR GmbH | Verfahren zur Herstellung von Polyolefinen mit breiter Molmassenverteilung |
| DE59204800D1 (de) | 1991-05-27 | 1996-02-08 | Hoechst Ag | Verfahren zur Herstellung von syndiotaktischen Polyolefinen mit breiter Molmassenverteilung |
| US5341124A (en) | 1991-05-29 | 1994-08-23 | Se-Kure Controls, Inc. | Mountable product sensor and display stand |
| DE4120009A1 (de) | 1991-06-18 | 1992-12-24 | Basf Ag | Loesliche katalysatorsysteme zur herstellung von polyalk-1-enen mit hohen molmassen |
| US5721185A (en) | 1991-06-24 | 1998-02-24 | The Dow Chemical Company | Homogeneous olefin polymerization catalyst by abstraction with lewis acids |
| US5594078A (en) | 1991-07-23 | 1997-01-14 | Phillips Petroleum Company | Process for producing broad molecular weight polyolefin |
| US5235081A (en) | 1992-03-18 | 1993-08-10 | Ethyl Corporation | Method of removing gel forming materials from methylaluminoxanes |
| US5308815A (en) | 1991-07-26 | 1994-05-03 | Ethyl Corporation | Heterogeneous methylaluminoxane catalyst system |
| US5157137A (en) | 1991-07-26 | 1992-10-20 | Ethyl Corporation | Method of making gel free alkylaluminoxane solutions |
| DE69225749T2 (de) | 1991-08-08 | 1998-10-01 | Rexene Corp | Harzzusammensetzung aus amorphem Polyolefin und crystallinem Polypropylen |
| TW300901B (https=) | 1991-08-26 | 1997-03-21 | Hoechst Ag | |
| NL9101502A (nl) | 1991-09-06 | 1993-04-01 | Dsm Nv | Werkwijze voor het bereiden van een gebrugde metalloceenverbinding alsmede een katalysatorcomponent en een werkwijze voor de polymerisatie van een olefinen. |
| CA2077744C (en) | 1991-09-30 | 2003-04-15 | Edwar Shoukri Shamshoum | Homogeneous-heterogeneous catalyst system for polyolefins |
| US5416228A (en) * | 1991-10-07 | 1995-05-16 | Fina Technology, Inc. | Process and catalyst for producing isotactic polyolefins |
| KR100236805B1 (ko) | 1991-10-15 | 2000-02-01 | 그레이스 스티븐 에스. | 금속 배위 착화합물의 제조방법 |
| EP0537686B1 (de) | 1991-10-15 | 2005-01-12 | Basell Polyolefine GmbH | Verfahren zur Herstellung eines Olefinpolymers unter Verwendung von Metallocenen mit speziell substituierten Indenylliganden |
| US5278272A (en) | 1991-10-15 | 1994-01-11 | The Dow Chemical Company | Elastic substantialy linear olefin polymers |
| US5233049A (en) | 1991-10-29 | 1993-08-03 | Occidental Chemical Corporation | Highly fluorinated bis-imides |
| US5281679A (en) | 1991-11-07 | 1994-01-25 | Exxon Chemical Patents Inc. | Catalyst and method of broadening polymer molecular weight distribution and increasing polymer tensile impact strength and products made thereof |
| US5359015A (en) | 1991-11-07 | 1994-10-25 | Exxon Chemical Patents Inc. | Metallocene catalysts and their production and use |
| DE69224600T2 (de) | 1991-11-12 | 1998-08-27 | Nippon Oil Co Ltd | Katalysatorbestandteile für Olefinpolymerisation |
| DE69224463T2 (de) | 1991-11-28 | 1998-07-09 | Showa Denko Kk | Neues Metallocen und Verfahren zur Herstellung von Polyolefinen unter Verwendung desselben |
| CA2125480C (en) | 1991-12-13 | 2003-06-24 | Patrick Brant | Ethylene/longer alpha-olefin copolymers |
| US6545088B1 (en) | 1991-12-30 | 2003-04-08 | Dow Global Technologies Inc. | Metallocene-catalyzed process for the manufacture of EP and EPDM polymers |
| DE69224287T2 (de) | 1992-01-06 | 1998-08-27 | The Dow Chemical Co., Midland, Mich. | Katalysatorzusammensetzung |
| US5391660A (en) | 1992-01-14 | 1995-02-21 | Nippon Oil Company, Limited | Process for preparing polyolefines |
| EP0552945B1 (en) * | 1992-01-23 | 1997-05-07 | Mitsui Petrochemical Industries, Ltd. | Process for the preparation of polyolefin |
| TW337527B (en) | 1992-01-24 | 1998-08-01 | Hoechst Ag | Catalyst for the polymerization of olefins, process for the preparation thereof, and use thereof |
| TW304963B (https=) | 1992-01-27 | 1997-05-11 | Hoechst Ag | |
| WO1993019103A1 (en) | 1992-03-16 | 1993-09-30 | Exxon Chemical Patents Inc. | IONIC CATALYST FOR THE PRODUCTION OF POLY-α-OLEFINS OF CONTROLLED TACTICITY |
| GB9205841D0 (en) | 1992-03-18 | 1992-04-29 | Exxon Chemical Patents Inc | Hydrocarbon resins,processes for their manufacture and adhesive compositions containing such resins |
| US5329032A (en) | 1992-03-18 | 1994-07-12 | Akzo Chemicals Inc. | Polymethylaluminoxane of enhanced solution stability |
| US5436304A (en) | 1992-03-19 | 1995-07-25 | Exxon Chemical Patents Inc. | Process for polymerizing monomers in fluidized beds |
| US5352749A (en) | 1992-03-19 | 1994-10-04 | Exxon Chemical Patents, Inc. | Process for polymerizing monomers in fluidized beds |
| US5374696A (en) | 1992-03-26 | 1994-12-20 | The Dow Chemical Company | Addition polymerization process using stabilized reduced metal catalysts |
| FI112233B (fi) | 1992-04-01 | 2003-11-14 | Basell Polyolefine Gmbh | Katalyytti olefiinipolymerointia varten, menetelmä sen valmistamiseksi ja sen käyttö |
| US5459217A (en) | 1993-04-09 | 1995-10-17 | Mitsui Petrochemical Industries, Ltd. | Ethylene/alpha-olefin copolymer |
| EP0578838A1 (en) | 1992-04-29 | 1994-01-19 | Hoechst Aktiengesellschaft | Olefin polymerization catalyst, process for its preparation, and its use |
| US5308817A (en) | 1992-05-18 | 1994-05-03 | Fina Technology, Inc. | Metallocene catalyst component with good catalyst efficiency after aging |
| 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 |
| BE1005957A5 (fr) | 1992-06-05 | 1994-04-05 | Solvay | Procede de preparation d'un systeme catalytique, procede de (co)polymerisation d'olefines et (co)polymeres d'au moins une olefine. |
| FI945873L (fi) | 1992-06-18 | 1994-12-14 | Spherilene Srl | Menetelmä etyleenisen polymeerin valmistamiseksi |
| US5710222A (en) | 1992-06-22 | 1998-01-20 | Fina Technology, Inc. | Method for controlling the melting points and molecular weights of syndiotactic polyolefins using metallocene catalyst systems |
| ES2137266T3 (es) | 1992-07-01 | 1999-12-16 | Exxon Chemical Patents Inc | Catalizadores de polimerizacion de olefinas a base de metales de transicion. |
| US5332707A (en) | 1992-07-31 | 1994-07-26 | Amoco Corporation | Olefin polymerization and copolymerization catalyst |
| JPH07509752A (ja) | 1992-08-05 | 1995-10-26 | エクソン・ケミカル・パテンツ・インク | オレフィン重合用の担持されたイオン遷移金属触媒 |
| ES2128371T3 (es) | 1992-08-15 | 1999-05-16 | Targor Gmbh | Procedimiento para la obtencion de poliolefinas. |
| US5248801A (en) | 1992-08-27 | 1993-09-28 | Ethyl Corporation | Preparation of methylaluminoxanes |
| DE4228812A1 (de) | 1992-08-29 | 1994-03-03 | Hoechst Ag | Siegelbare Polypropylen-Mehrschichtfolie, Verfahren zu ihrer Herstellung und ihre Verwendung |
| EP0586168B1 (en) | 1992-09-04 | 2000-07-05 | BP Chemicals Limited | Catalyst compositions and process for preparing polyolefins |
| JP3355534B2 (ja) * | 1992-09-10 | 2002-12-09 | 住友化学工業株式会社 | エチレン−αオレフィン共重合体及び該共重合体を用いて成形されてなる成形体 |
| RU95110681A (ru) | 1992-09-29 | 1997-01-10 | Эксон Кемикэл Пейтентс Инк. (US) | Разветвленные длинноцепочечные полимеры и способ получения разветвленных длинноцепочечных полимеров |
| EP0662979B1 (en) | 1992-10-02 | 1997-07-16 | The Dow Chemical Company | Supported homogeneous catalyst complexes for olefin polymerization |
| US5317036A (en) | 1992-10-16 | 1994-05-31 | Union Carbide Chemicals & Plastics Technology Corporation | Gas phase polymerization reactions utilizing soluble unsupported catalysts |
| US5939346A (en) | 1992-11-02 | 1999-08-17 | Akzo Nobel N.V. | Catalyst system comprising an aryloxyaluminoxane containing an electron withdrawing group |
| US5391793A (en) | 1992-11-02 | 1995-02-21 | Akzo Nobel N.V. | Aryloxyaluminoxanes |
| CA2103401C (en) | 1992-11-19 | 2002-12-17 | Mamoru Takahashi | Ethylene copolymer composition |
| 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 |
| CA2103379C (en) | 1992-11-19 | 2000-05-23 | Toshiyuki Tsutsui | Catalyst for olefin polymerization, process for olefin polymerization using the same, ethylene/.alpha.-olefin copolymer, graft modified ethylene/.alpha.-olefin copolymer, and ethylene copolymer composition |
| AU5416394A (en) | 1992-11-24 | 1994-06-22 | Debiopharm S.A. | Cisplatinum/oxaliplatinum combination |
| BE1006438A3 (fr) | 1992-12-17 | 1994-08-30 | Solvay | Systeme catalytique, utilisation de ce systeme catalytique pour la (co)polymerisation d'olefines, procede de preparation de ce systeme catalytique et procede de (co)polymerisation d'olefines. |
| CA2110654C (en) | 1992-12-17 | 2006-03-21 | Albert Rossi | Dilute process for the polymerization of ethylene/alpha-olefin copolymer using metallocene catalyst systems |
| IT1256260B (it) * | 1992-12-30 | 1995-11-29 | Montecatini Tecnologie Srl | Polipropilene atattico |
| DE69412954T2 (de) | 1993-01-11 | 1999-03-11 | Mitsui Chemicals, Inc., Tokio/Tokyo | Propylenpolymer zusammensetzung |
| GB9300934D0 (en) | 1993-01-19 | 1993-03-10 | Bp Chem Int Ltd | Metallocene complexes |
| US5914376A (en) | 1993-01-21 | 1999-06-22 | Targor Gmbh | Catalyst for the polymerization of olefins, process for the preparation thereof, and use thereof |
| US5391529A (en) | 1993-02-01 | 1995-02-21 | Albemarle Corporation | Siloxy-aluminoxane compositions, and catalysts which include such compositions with a metallocene |
| ES2178648T3 (es) | 1993-02-05 | 2003-01-01 | Idemitsu Kosan Co | Polietileno, composicion de resina termoplastica que lo contiene, y procedimiento de produccion de polietileno. |
| TW298593B (https=) | 1993-02-12 | 1997-02-21 | Hoechst Ag | |
| JP3307704B2 (ja) | 1993-02-19 | 2002-07-24 | 三菱化学株式会社 | α‐オレフィン重合体の製造法 |
| DE69430910T2 (de) | 1993-02-22 | 2002-12-12 | Idemitsu Kosan Co. Ltd., Tokio/Tokyo | Ethylencopolymer, dieses enthaltende thermoplastische harzzusammensetzung und verfahren zu seiner herstellung |
| US6313240B1 (en) | 1993-02-22 | 2001-11-06 | Tosoh Corporation | Process for producing ethylene/α-olefin copolymer |
| BE1006880A3 (fr) * | 1993-03-01 | 1995-01-17 | Solvay | Precurseur solide d'un systeme catalytique pour la polymerisation d'olefines, procede pour sa preparation, systeme catalytique comprenant ce precurseur solide et procede de polymerisation d'olefines en presence de ce systeme catalytique. |
| JP3352494B2 (ja) | 1993-03-25 | 2002-12-03 | 三井鉱山株式会社 | 窒素酸化物分解触媒及びそれを用いた脱硝方法 |
| PT619325E (pt) | 1993-04-07 | 2002-02-28 | Atofina Res | Processo e catalisadores para a producao de olefinas |
| US5859088A (en) | 1993-04-13 | 1999-01-12 | Minnesota Mining And Manufacturing Company | Radiation-curable poly(α-olefin) adhesives |
| CA2118777A1 (en) | 1993-04-13 | 1994-10-14 | Gaddam N. Babu | Radiation-curable poly(alpha-olefin) adhesives |
| US5462999A (en) | 1993-04-26 | 1995-10-31 | Exxon Chemical Patents Inc. | Process for polymerizing monomers in fluidized beds |
| JP3077940B2 (ja) | 1993-04-26 | 2000-08-21 | エクソン・ケミカル・パテンツ・インク | 流動層重合法のための安定な操作条件を決定する方法 |
| GB9308669D0 (en) | 1993-04-27 | 1993-06-09 | Du Pont Canada | Grafting of monomers onto polyolefins in presence of organic peroxides |
| US5643846A (en) | 1993-04-28 | 1997-07-01 | Fina Technology, Inc. | Process for a isotactic/syndiotactic polymer blend in a single reactor |
| US5346963A (en) | 1993-04-28 | 1994-09-13 | The Dow Chemical Company | Graft-modified, substantially linear ethylene polymers and methods for their use |
| US5804524A (en) | 1993-04-28 | 1998-09-08 | Fina Technology, Inc. | Process for a isotactic/syndiotactic polymer blend in a single reactor |
| KR100329889B1 (ko) | 1993-05-13 | 2002-12-06 | 엑손 케미칼 패턴츠 인코포레이티드 | 좁은조성분포를갖는에틸렌공중합체,그의제조방법및용도 |
| BE1007148A3 (fr) | 1993-05-17 | 1995-04-11 | Solvay | Support pour catalyseurs, procede pour la fabrication d'un gel precurseur d'un support pour catalyseurs, procede de preparation d'un support pour catalyseurs, catalyseur pour la polymerisation d'olefines et procede pour la polymerisation d'olefines au moyen de ce catalyseur. |
| ZA943399B (en) | 1993-05-20 | 1995-11-17 | Bp Chem Int Ltd | Polymerisation process |
| BE1007040A3 (fr) | 1993-05-25 | 1995-02-28 | Solvay | Support de catalyseur et catalyseur de polymerisation des alpha-olefines; procedes pour leur obtention et polymerisation des alpha-olefines en presence du catalyseur. |
| EP0629631B1 (en) * | 1993-06-07 | 2002-08-28 | Mitsui Chemicals, Inc. | Novel transition metal compound, and polymerization catalyst containing it |
| EP0812854B2 (en) | 1993-06-07 | 2011-04-20 | Mitsui Chemicals, Inc. | Novel transition metal compound, olefin polymerization catalyst comprising said compound, process for olefin polymerization using said catalyst and propylene homo- and copolymer |
| US5354721A (en) * | 1993-06-22 | 1994-10-11 | Phillips Petroleum Company | Organo-aluminoxy product and use |
| BR9407034A (pt) | 1993-06-24 | 1996-03-19 | Dow Chemical Co | Complexos de titânio ( I) ou zircônio (II) e catalisadores de polimerização por adição dos mesmos |
| ES2141833T3 (es) | 1993-08-06 | 2000-04-01 | Exxon Chemical Patents Inc | Catalizadores de polimerizacion, su produccion y uso. |
| US5539069A (en) | 1993-08-10 | 1996-07-23 | Mitsui Petrochemical Industries, Ltd. | Olefin polymerization catalysts and methods of olefin polymerization |
| US5700895A (en) | 1993-08-23 | 1997-12-23 | Sumitomo Chemical Company, Limited | Ethylene-α-olefin copolymer and molded article thereof |
| DE4328571C1 (de) | 1993-08-25 | 1994-10-27 | Daimler Benz Ag | Aufsteller zum Halten eines Flügels in verschiedenen Öffnungsstellungen relativ zu seinem Rahmen |
| US5455214A (en) | 1993-09-09 | 1995-10-03 | Mobil Oil Corporation | Metallocenes supported on ion exchange resins |
| DE4330661A1 (de) * | 1993-09-10 | 1995-03-16 | Basf Ag | Kälteschlagzähe Propylenpolymerisate |
| IT1271406B (it) | 1993-09-13 | 1997-05-28 | Spherilene Srl | Procedimento per la preparazione di polimeri dell'etilene e prodotti ottenuti |
| US5631202A (en) * | 1993-09-24 | 1997-05-20 | Montell Technology Company B.V. | Stereospecific metallocene catalysts with stereolocking α-CP substituents |
| DE4333128A1 (de) | 1993-09-29 | 1995-03-30 | Hoechst Ag | Verfahren zur Herstellung von Polyolefinen |
| DE4333569A1 (de) | 1993-10-01 | 1995-04-06 | Hoechst Ag | Verfahren zur Olefinpolymerisation |
| DE4334045A1 (de) | 1993-10-06 | 1995-04-13 | Bayer Ag | Katalysator, dessen Herstellung und Verwendung zur Gasphasenpolymerisation von konjugierten Dienen |
| WO1995010575A1 (en) | 1993-10-13 | 1995-04-20 | Exxon Chemical Patents Inc. | Adhesives from low molecular weight polypropylene |
| US5576259A (en) | 1993-10-14 | 1996-11-19 | Tosoh Corporation | Process for producing α-olefin polymer |
| GB9321251D0 (en) | 1993-10-14 | 1993-12-01 | Du Pont Canada | Bounding polyvinyl chloride to cellulosic material |
| US5817590A (en) | 1993-10-14 | 1998-10-06 | Tosoh Corporation | Catalyst for αE --olefin polymerization containing a Lewis base |
| US5670438A (en) | 1993-10-27 | 1997-09-23 | Phillips Petroleum Company | Catalyst compositions and catalytic processes |
| JP3423378B2 (ja) | 1993-11-12 | 2003-07-07 | 三井化学株式会社 | 新規な遷移金属化合物および該遷移金属化合物からなるオレフィン重合用触媒成分、該オレフィン重合用触媒成分を含むオレフィン重合用触媒ならびにオレフィンの重合方法 |
| EP0729477B1 (en) | 1993-11-19 | 1999-10-27 | Exxon Chemical Patents Inc. | Polymerization catalyst systems, their production and use |
| EP0654476B1 (de) | 1993-11-24 | 2001-01-24 | TARGOR GmbH | Metallocene, Verfahren zu ihrer Herstellung und ihrer Verwendung als Katalysatoren |
| JPH07144455A (ja) | 1993-11-25 | 1995-06-06 | Canon Inc | インクジェット記録装置 |
| FI95276C (fi) | 1993-12-03 | 1996-01-10 | Borealis As | Olefiinien polymerointikatalyytti ja menetelmä sen valmistamiseksi |
| WO1995015985A1 (en) | 1993-12-08 | 1995-06-15 | Asahi Kasei Kogyo Kabushiki Kaisha | Novel olefin polymerization catalyst and process for polymerizing olefin by using the same |
| FI945958A7 (fi) | 1993-12-21 | 1995-06-22 | Targor Gmbh | Menetelmä polyolefiinien valmistamiseksi |
| DE69406637T2 (de) | 1993-12-22 | 1998-03-19 | Sumitomo Chemical Co | Schichtfilm aus Polypropylen |
| DE4344688A1 (de) | 1993-12-27 | 1995-06-29 | Hoechst Ag | Metallocenverbindung |
| EP0664304B1 (en) | 1993-12-27 | 1999-08-04 | Mitsui Chemicals, Inc. | Olefin polymerization catalyst and process for olefin polymerization |
| DE4344689A1 (de) * | 1993-12-27 | 1995-06-29 | Hoechst Ag | Metallocenverbindung |
| EP0737694B1 (en) | 1993-12-28 | 2001-06-06 | Idemitsu Kosan Company Limited | Process for producing olefin polymer and ethylene polymer |
| US6214949B1 (en) * | 1993-12-29 | 2001-04-10 | Fina Technology, Inc. | Polymerization of polyolefins having low melt flow and high molecular weight |
| EP0664301A1 (en) | 1994-01-24 | 1995-07-26 | Dainichiseika Color & Chemicals Mfg. Co. Ltd. | Chitosan derivatives, preparation process thereof and cosmetic compositions containing same |
| CA2142748C (en) * | 1994-02-18 | 1999-02-23 | Shin-Ichi Kojoh | Ethylene polymer and process for preparing the same |
| US5447895A (en) | 1994-03-10 | 1995-09-05 | Northwestern University | Sterically shielded diboron-containing metallocene olefin polymerization catalysts |
| GB9404708D0 (en) | 1994-03-11 | 1994-04-27 | Du Pont Canada | Polypropylene-based hot-melt adhesive |
| US5594080A (en) | 1994-03-24 | 1997-01-14 | Leland Stanford, Jr. University | Thermoplastic elastomeric olefin polymers, method of production and catalysts therefor |
| US5410003A (en) * | 1994-03-31 | 1995-04-25 | Union Carbide Chemicals & Plastics Technology Corporation | Process for production of homogeneous polyethylenes |
| KR100388331B1 (ko) | 1994-04-11 | 2003-10-11 | 미쓰이 가가쿠 가부시키가이샤 | 프로필렌중합체조성물의제조방법및프로필렌중합체조성물 |
| CN1104444C (zh) * | 1994-04-11 | 2003-04-02 | 三井化学株式会社 | 丙烯聚合物组合物的制备方法 |
| WO1996020225A2 (en) | 1994-12-20 | 1996-07-04 | Montell Technology Company B.V. | Reactor blend polypropylene, process for the preparation thereof and process for preparing metallocene ligands |
| DE69503560T2 (de) | 1994-04-28 | 1999-03-18 | Sumitomo Chemical Co., Ltd., Osaka | Polypropylen-Zusammensetzung für laminatete und orientierte Filme sowie daraus bestehender laminateter und orientierter Film |
| DE69522806T2 (de) | 1994-06-24 | 2002-05-16 | Exxonmobil Chemical Patents Inc., Baytown | Monocyclopentadienyl-metalverbindungen als katalysatoren zur produktion von ethylen-alpha-olefincopolymeren |
| US5486632A (en) | 1994-06-28 | 1996-01-23 | The Dow Chemical Company | Group 4 metal diene complexes and addition polymerization catalysts therefrom |
| IT1270070B (it) | 1994-07-08 | 1997-04-28 | Spherilene Srl | Componenti e catalizzatori per la polimerizzazione di olefine |
| US5552489A (en) | 1994-07-22 | 1996-09-03 | Exxon Chemical Patents Inc. | Tackifiers and a process to obtain tackifiers |
| DE4431644A1 (de) | 1994-08-01 | 1996-03-07 | Danubia Petrochem Deutschland | Katalysatorsystem und Verfahren zur Polymerisation von Olefinen |
| US5453471B1 (en) | 1994-08-02 | 1999-02-09 | Carbide Chemicals & Plastics T | Gas phase polymerization process |
| US5527929A (en) | 1994-08-02 | 1996-06-18 | The Dow Chemical Company | Zwitterionic biscyclopentadienyl complexes |
| US5516583A (en) * | 1994-08-29 | 1996-05-14 | E. I. Du Pont De Nemours And Company | Adhesive for tamper evident seals |
| DE4431838A1 (de) | 1994-09-07 | 1996-03-14 | Basf Ag | Geträgerte Metallocen-Katalysatorsysteme |
| US5625087A (en) | 1994-09-12 | 1997-04-29 | The Dow Chemical Company | Silylium cationic polymerization activators for metallocene complexes |
| US5763543A (en) | 1994-09-14 | 1998-06-09 | Exxon Chemical Patents Inc. | Olefin polymerization process with little or no scavenger present |
| TW369547B (en) | 1994-09-21 | 1999-09-11 | Mitsui Chemicals Inc | Olefin polymerization catalyst and process for olefin polymerization |
| US5529943A (en) | 1994-09-30 | 1996-06-25 | United Microelectronics Corporation | Method of making buried bit line ROM with low bit line resistance |
| DE4436113A1 (de) | 1994-10-10 | 1996-04-11 | Hoechst Ag | Metallocenverbindung |
| US6300451B1 (en) | 1994-10-24 | 2001-10-09 | Exxon Chemical Patents Inc. | Long-chain branched polymers and their production |
| WO1996013531A1 (en) | 1994-10-31 | 1996-05-09 | W.R. Grace & Co.-Conn. | Preparation of modified polyolefin catalysts and in situ preparation of supported metallocene and ziegler-natta/metallocene polyolefin catalysts |
| US5430070A (en) | 1994-12-16 | 1995-07-04 | Ryusuke Kono | Functional insulation resin composition |
| US5539124A (en) | 1994-12-19 | 1996-07-23 | Occidental Chemical Corporation | Polymerization catalysts based on transition metal complexes with ligands containing pyrrolyl ring |
| TW383313B (en) | 1994-12-20 | 2000-03-01 | Mitsui Petrochemical Ind | Preparation of ethylene-alpha-olefin-nonconjugate polyene random copolymers, the copolymers obtaining which, and the use of the copolymers |
| DE69525228T2 (de) | 1994-12-20 | 2002-07-11 | Sumitomo Rubber Industries Ltd., Kobe | Gummimischung für Reifenlaufflächen |
| 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 |
| SG38896A1 (en) | 1994-12-22 | 1997-04-17 | Sumitomo Chemical Co | Polypropylene composition and laminated and oriented film therefrom |
| CN1171097A (zh) | 1994-12-26 | 1998-01-21 | 三井石油化学工业株式会社 | 含链多烯基的降冰片烯化合物和用其制得的不饱和乙烯共聚物 |
| DE4446923A1 (de) | 1994-12-28 | 1996-07-04 | Hoechst Ag | Polyolefinwachs |
| ES2116188B1 (es) | 1994-12-30 | 1999-04-01 | Repsol Quimica Sa | Proceso de obtencion de poliolefinas con distribuciones de pesos moleculares anchas, bimodales o multimodales. |
| US5554775A (en) | 1995-01-17 | 1996-09-10 | Occidental Chemical Corporation | Borabenzene based olefin polymerization catalysts |
| EP0805826B1 (en) | 1995-01-24 | 2003-04-23 | E.I. Du Pont De Nemours And Company | Olefin polymers |
| US6495646B1 (en) | 1995-01-24 | 2002-12-17 | E. I. Du Pont De Nemours And Company | Polyolefins with new structures |
| US6482907B1 (en) | 1995-01-24 | 2002-11-19 | E.I. Du Pont De Nemours And Company | Polymerization of olefins |
| US5880241A (en) | 1995-01-24 | 1999-03-09 | E. I. Du Pont De Nemours And Company | Olefin polymers |
| US5539056A (en) | 1995-01-31 | 1996-07-23 | Exxon Chemical Patents Inc. | Thermoplastic elastomers |
| US5516848A (en) * | 1995-01-31 | 1996-05-14 | Exxon Chemical Patents Inc. | Process to produce thermoplastic elastomers |
| EP0807096A1 (de) | 1995-02-01 | 1997-11-19 | Basf Aktiengesellschaft | Verfahren zur herstellung von olefin-oligomeren |
| JP3535934B2 (ja) * | 1995-02-07 | 2004-06-07 | 三井化学株式会社 | オレフィン重合体の製造方法 |
| US6063838A (en) * | 1995-02-16 | 2000-05-16 | 3M Innovative Properties Company | Blended pressure-sensitive adhesives |
| EP0728773B1 (en) | 1995-02-21 | 1998-11-04 | Mitsubishi Chemical Corporation | Catalysts for olefin polymerization and a process for preparing olefin polymers therewith |
| KR100506376B1 (ko) | 1995-02-23 | 2005-08-10 | 애이취 . 비. 풀러. 라이센싱 앤드 파이년싱, 인코포레이티드 | 직물제품 및 일회용 위생제품 |
| EP0891991A3 (en) | 1995-03-01 | 1999-02-24 | Minnesota Mining And Manufacturing Company | Tris(pentafluorophenyl)borate complexes and catalysts derived therefrom |
| US5599881A (en) | 1995-03-07 | 1997-02-04 | Dupont Canada Inc. | Nucleophilic amine functionalized polyolefin |
| CN1116309C (zh) | 1995-03-10 | 2003-07-30 | 陶氏环球技术公司 | 负载型催化剂组分、负载型催化剂及制备方法,聚合方法,配位化合物及其制备方法 |
| ATE210214T1 (de) | 1995-03-17 | 2001-12-15 | Bp Corp North America Inc | Teppich und teppichrücken dafür |
| WO1996030418A1 (en) | 1995-03-27 | 1996-10-03 | E.I. Du Pont De Nemours And Company | Polychloroprene composition |
| US5527846A (en) | 1995-03-27 | 1996-06-18 | E. I. Du Pont De Nemours And Company | Polychloroprene adhesive latex composition |
| NO315857B1 (no) | 1995-03-28 | 2003-11-03 | Japan Polyolefines Co Ltd | Etylen-<alfa>-olefin-kopolymer, blanding, film, laminert material, elektrisk isolerende material og strömkabel inneholdende denne |
| US5616661A (en) | 1995-03-31 | 1997-04-01 | Union Carbide Chemicals & Plastics Technology Corporation | Process for controlling particle growth during production of sticky polymers |
| US5637660A (en) | 1995-04-17 | 1997-06-10 | Lyondell Petrochemical Company | Polymerization of α-olefins with transition metal catalysts based on bidentate ligands containing pyridine or quinoline moiety |
| US5696213A (en) | 1995-04-21 | 1997-12-09 | Exxon Chemical Patents Inc. | Ethylene-α-olefin-diolefin elastomers solution polymerization process |
| WO1996034021A1 (en) | 1995-04-25 | 1996-10-31 | Lyondell Petrochemical Company | Azaborolinyl metal complexes as olefin polymerization catalysts |
| DE69603850T2 (de) | 1995-05-22 | 2000-04-13 | Minnesota Mining And Mfg. Co., Saint Paul | Schutzhaftgegenstand |
| US6352948B1 (en) * | 1995-06-07 | 2002-03-05 | Kimberly-Clark Worldwide, Inc. | Fine fiber composite web laminates |
| US5767031A (en) | 1995-06-07 | 1998-06-16 | Fina Technology, Inc. | Ziegler-Natta catalysts modified with metallocenes |
| US5618883A (en) * | 1995-06-07 | 1997-04-08 | Avery Dennison Corporation | Styrene ethylene-butylene and ethylene-propylene block copolymer hot melt pressure sensitive adhesives |
| US6407177B1 (en) | 1995-06-07 | 2002-06-18 | Fina Technology, Inc. | Polypropylene blend |
| JP3281389B2 (ja) | 1995-06-08 | 2002-05-13 | 昭和電工株式会社 | イオン性化合物およびその化合物を用いたオレフィン重合用触媒 |
| DE59600760D1 (de) | 1995-06-12 | 1998-12-10 | Targor Gmbh | Übergangsmetallverbindung |
| TW326450B (en) | 1995-06-28 | 1998-02-11 | Mitsui Petroleum Chemicals Ind | Ethylene copolymer rubber, vulcanizable rubber composition containing the copolymer rubber, and process for preparing the same |
| IT1275777B1 (it) | 1995-07-06 | 1997-10-17 | Enichem Spa | Catalizzatore metallocenico per la (co)polimerizzazione delle olefine |
| SG64939A1 (en) | 1995-07-17 | 2002-02-19 | Mitsui Chemicals Inc | Olefin polymerization catalyst, process for preparing olefin polymer, and olefin polymer |
| US5720543A (en) | 1995-07-19 | 1998-02-24 | Diamondlight Industries, Inc. | Portable flashlight |
| US5731253A (en) | 1995-07-27 | 1998-03-24 | Albemarle Corporation | Hydrocarbylsilloxy - aluminoxane compositions |
| DE19527652A1 (de) * | 1995-07-28 | 1997-01-30 | Hoechst Ag | Metallocenverbindung |
| IT1277468B1 (it) | 1995-08-09 | 1997-11-10 | Enichem Spa | Catalizzatore per la (co)polimerizzazione delle olefine e procedimento impiegante lo stesso |
| US5900517A (en) | 1995-08-30 | 1999-05-04 | Enichem S.P.A. | Cyclopentadienyl derivatives and process for their preparation |
| JP3264148B2 (ja) * | 1995-08-31 | 2002-03-11 | 住友化学工業株式会社 | プロピレン−エチレンランダム共重合体、その製法及びフィルム |
| CA2157806A1 (en) | 1995-09-08 | 1997-03-09 | David John Mitchell | Polypropylene-based hot-melt adhesive |
| DE69602329T2 (de) | 1995-09-14 | 1999-09-23 | Showa Denko K.K., Tokio/Tokyo | Katalysator für ethylenische Polymerisation |
| ATE245665T1 (de) | 1995-09-28 | 2003-08-15 | Basell Polyolefine Gmbh | Geträgertes katalysatorsystem, verfahren zu seiner herstellung und seine verwendung zur polymerisation von olefinen |
| US5795941A (en) | 1995-10-03 | 1998-08-18 | The Dow Chemical Company | Crosslinkable bimodal polyolefin compositions |
| JP3582181B2 (ja) | 1995-10-04 | 2004-10-27 | 住友化学工業株式会社 | オレフィン重合触媒用担体、オレフィン重合触媒及びオレフィン重合体の製造方法 |
| CA2233658A1 (en) | 1995-10-06 | 1997-04-10 | The Dow Chemical Company | Branched block ethylene polymers, their preparation and compositions comprising the same |
| EP0768322A1 (en) | 1995-10-16 | 1997-04-16 | Sumitomo Chemical Company, Limited | Method for preparing catalyst component for olefin polymerization, catalyst for olefin polymerization and process for producing olefin polymer with the catalyst |
| BR9611188A (pt) | 1995-10-27 | 1999-03-30 | Dow Chemical Co | Complexo metálico sistema catalisador e processo para polimerizar uma alpha-olefina |
| US5869585A (en) | 1995-10-30 | 1999-02-09 | Mobil Oil Corporation | Multi-component catalyst systems for olefin polymerization |
| GB9522859D0 (en) | 1995-11-08 | 1996-01-10 | Borealis As | Compounds |
| US5693838A (en) | 1995-11-13 | 1997-12-02 | Albemarle Corporation | Aluminoxane process and product |
| US6066588A (en) | 1995-11-22 | 2000-05-23 | Fina Research, S.A. | Bridged metallocenes catalyst for polymerization of olefins |
| JP2000502130A (ja) | 1995-12-07 | 2000-02-22 | エクソン・ケミカル・パテンツ・インク | 粘着付与剤及び粘着付与剤を得る方法 |
| DE19546501A1 (de) * | 1995-12-13 | 1997-06-19 | Hoechst Ag | Metallocenverbindung |
| WO1997022639A1 (en) | 1995-12-19 | 1997-06-26 | Exxon Chemical Patents Inc. | High temperature solution polymerization process |
| US5876855A (en) | 1995-12-22 | 1999-03-02 | Minnesota Mining And Manufacturing Company | Pressure-sensitive adhesive suitable for skin and method of preparing |
| NZ316689A (en) | 1995-12-22 | 1999-04-29 | Minnesota Mining & Mfg | Blended pressure-sensitive adhesives comprising two components, one being pressure sensitive and the other being a thermoplastic material |
| US5760028A (en) * | 1995-12-22 | 1998-06-02 | The Dupont Merck Pharmaceutical Company | Integrin receptor antagonists |
| ID16442A (id) | 1996-01-22 | 1997-10-02 | Dow Chemical Co | Polimer etilena berat molekul ultra rendah |
| US6114477A (en) | 1996-02-09 | 2000-09-05 | Exxon Chemical Patents Inc. | Polymerization process |
| DE19606165A1 (de) | 1996-02-20 | 1997-08-21 | Basf Ag | Verfahren zur Herstellung von Polymerisaten von Alkenen durch Gasphasenpolymerisation |
| US5856256A (en) | 1996-02-20 | 1999-01-05 | Northwestern University | Organo-Lewis acid as cocatalyst for cationic homogeneous Ziegler-Natta olefin polymerizations |
| DE19606167A1 (de) * | 1996-02-20 | 1997-08-21 | Basf Ag | Geträgerte Katalysatorsysteme |
| DE19606166A1 (de) | 1996-02-20 | 1997-08-21 | Basf Ag | Verfahren zur Herstellung von Polymerisaten von Alkenen durch Suspensionspolymerisation |
| IT1282666B1 (it) | 1996-02-22 | 1998-03-31 | Enichem Spa | Catalizzatore metallocenico sostituito per la (co) polimerizzazione delle olefine |
| ID17196A (id) | 1996-03-14 | 1997-12-11 | Dow Chemical Co | Bahan-bahan perekat yang mengandung polimer-polimer olefin |
| US6107430A (en) | 1996-03-14 | 2000-08-22 | The Dow Chemical Company | Low application temperature hot melt adhesive comprising ethylene α-olefin |
| WO1998041574A1 (en) | 1997-03-14 | 1998-09-24 | H.B. Fuller Licensing & Financing, Inc. | FOAMABLE COMPOSITIONS COMPRISING LOW VISCOSITY THERMOPLASTIC MATERIAL COMPRISING AN ETHYLENEα-OLEFIN |
| AR006240A1 (es) | 1996-03-14 | 1999-08-11 | Fuller H B Licensing Financ | Adhesivo de fusion caliente que comprende interpolimeros, articulo no tejido que lo comprende, procedimiento de polimerizacion para preparlo y caja, envase, bandeja y libro unidos con dicho adhesivo |
| US5756141A (en) * | 1996-03-20 | 1998-05-26 | Chen; Chin Shu | Method for producing ready to pour frozen concentrated clarified fruit juice, fruit juice produced therefrom, and high solids fruit product |
| JP2000517349A (ja) | 1996-03-27 | 2000-12-26 | ザ ダウ ケミカル カンパニー | 分散した触媒活性剤による溶液重合法 |
| ES2152653T3 (es) | 1996-03-29 | 2001-02-01 | Dow Chemical Co | Cocatalizador de metaloceno. |
| EP0891381B2 (en) | 1996-04-01 | 2006-05-24 | The Dow Chemical Company | Olefin solution polymerization |
| US5977251A (en) | 1996-04-01 | 1999-11-02 | The Dow Chemical Company | Non-adiabatic olefin solution polymerization |
| US6114261A (en) | 1996-04-15 | 2000-09-05 | Ato Findley, Inc. | Nonwoven absorbent article containing an emollient resistant polybutylene-based hot melt adhesive |
| US5763516A (en) | 1996-04-24 | 1998-06-09 | H.B. Fuller Licensing & Financing, Inc. | Polyethylene based hot-melt adhesive |
| US5744417A (en) | 1996-05-02 | 1998-04-28 | Lyondell Petrochemical Company | Supported catalyst |
| DE19622481A1 (de) * | 1996-06-05 | 1997-12-11 | Hoechst Ag | Geträgertes Katalysatorsystem, Verfahren zu seiner Herstellung und seine Verwendung zur Polymerisation von Olefinen |
| DE19624581C2 (de) | 1996-06-20 | 1999-02-04 | Targor Gmbh | Übergangsmetallverbindung und ein Verfahren zu ihrer Herstellung, sowie ihre Verwendung |
| US6166161A (en) | 1996-06-24 | 2000-12-26 | The Dow Chemical Company | Incorporation of functionalized comonomers in polyolefins |
| US6174974B1 (en) | 1996-07-05 | 2001-01-16 | Bayer Aktiengesellschaft | Method for producing thermoplastic elastomers |
| US5731451A (en) | 1996-07-12 | 1998-03-24 | Akzo Nobel Nv | Modified polyalkylauminoxane composition formed using reagent containing aluminum trialkyl siloxide |
| US6150498A (en) | 1996-07-12 | 2000-11-21 | The Dow Chemical Company | Polymer recovery |
| ES2187797T3 (es) | 1996-07-22 | 2003-06-16 | Dow Chemical Co | Adhesivos de fusion en caliente. |
| DE69715213T2 (de) | 1996-07-23 | 2003-04-30 | The Dow Chemical Co., Midland | Olefinpolymerisationkatalysatorzusammensetzung die eine verbindung der gruppe 13 enthält |
| US5861474A (en) | 1996-07-23 | 1999-01-19 | The Dow Chemical Company | Polymer devolatilization |
| US6297301B1 (en) | 1996-08-06 | 2001-10-02 | Exxonmobil Chemical Patents Inc. | Thermoplastic elastomer compositions having improved processing properties |
| US5939503A (en) | 1996-08-09 | 1999-08-17 | California Institute Of Technology | Group IV zwitterion ansa metallocene (ZAM) catalysts for α-olefin polymerization |
| ES2160289T3 (es) | 1996-08-13 | 2001-11-01 | Basell Polyolefine Gmbh | Sistema catalizador soportado, un procedimiento para su obtencion y su empleo para la polimerizacion de olefinas. |
| ATE325821T1 (de) | 1996-08-13 | 2006-06-15 | Basell Polyolefine Gmbh | Geträgerte chemische verbindung |
| US5854166A (en) | 1996-08-19 | 1998-12-29 | Northwestern University | Synthesis and use of (perfluoroaryl) fluoro-aluminate anion |
| DE19654921A1 (de) | 1996-08-29 | 1998-03-05 | Hoechst Ag | Polyolfinformmasse zur Herstellung von Vliesen |
| US6583227B2 (en) | 1996-09-04 | 2003-06-24 | Exxonmobil Chemical Patents Inc. | Propylene polymers for films |
| WO1998009996A1 (en) | 1996-09-06 | 1998-03-12 | Hyundai Petrochemical Co., Ltd. | Catalyst system for (co)polymerization of olefins and process for the preparation of olefin (co)polymers using the catalyst system |
| EP0925312A1 (en) | 1996-09-12 | 1999-06-30 | BP Chemicals Limited | Polymerisation catalyst |
| US5986651A (en) | 1996-09-23 | 1999-11-16 | Motorola, Inc. | Method, system, and article of manufacture for producing a network navigation device |
| US5847177A (en) | 1996-10-10 | 1998-12-08 | Albemarle Corporation | Production of hydrocarbon-soluble hydrocarbylaluminoxanes |
| WO1998016311A1 (en) | 1996-10-15 | 1998-04-23 | Northwestern University | Phenolate constrained geometry metallocene olefin polymerization catalyst, method of making, and method of using |
| US5744656A (en) | 1996-10-25 | 1998-04-28 | Boulder Scientific Company | Conversion of hexafluorobenzene to bromopentafluorobenzene |
| DE69705186T2 (de) | 1996-10-30 | 2002-03-14 | Repsol Quimica S.A., Madrid | Katalysatorsysteme für die (Co)Polymerisation von Alpha-Olefinen |
| DE19644041A1 (de) | 1996-10-31 | 1998-05-07 | Hoechst Ag | Metallocenen mit teilhydrierten pi-Liganden |
| DE19644039A1 (de) | 1996-10-31 | 1998-05-07 | Hoechst Ag | Metallocene |
| SG60151A1 (en) | 1996-11-15 | 1999-02-22 | Sumitomo Chemical Co | Propylene-1-butene copolymer |
| TR199901635T2 (xx) | 1996-11-15 | 2000-02-21 | Montell Technology Company Bv | Heterosiklik metalosenler ve polimerizasyon kataliz�rleri. |
| DE19648895A1 (de) | 1996-11-26 | 1998-05-28 | Clariant Gmbh | Polar modifizierte Polypropylen-Wachse |
| WO1998023690A1 (en) | 1996-11-27 | 1998-06-04 | Eastman Chemical Company | Method for preparing light-absorbing polymeric compositions |
| DE19654961C2 (de) | 1996-12-12 | 1999-04-29 | Basf Ag | Verfahren für die Herstellung von Copolymerisaten aus Kohlenmonoxid und olefinisch ungesättigten Verbindungen |
| US6245856B1 (en) | 1996-12-17 | 2001-06-12 | Exxon Chemical Patents, Inc. | Thermoplastic olefin compositions |
| US6177377B1 (en) * | 1996-12-18 | 2001-01-23 | Amherst Polymer Technology, Inc. | Polymer blends and process for preparation |
| US5849655A (en) | 1996-12-20 | 1998-12-15 | Fina Technology, Inc. | Polyolefin catalyst for polymerization of propylene and a method of making and using thereof |
| US5847059A (en) | 1996-12-20 | 1998-12-08 | Fina Technology, Inc. | Catalyst yield from supported metallocene catalysts |
| BR9714100A (pt) | 1996-12-26 | 2000-03-21 | Du Pont Canada | edação de uma camada de resina e processo aperfeiçoado para produção de embalagens carregadas com um material fluìvel |
| US6100351A (en) | 1997-01-07 | 2000-08-08 | Huntsman Polymers Corporation | Olefin polymerization process and products thereof |
| US5854363A (en) | 1997-01-08 | 1998-12-29 | Phillips Petroleum Company | (Omega-alkenyl) (cyclopentacarbyl) metallocene compounds |
| US5856547A (en) | 1997-01-08 | 1999-01-05 | Phillips Petroleum Company | Organo omega-alkenyl cyclopentacarbyl silane compounds |
| WO1998030629A1 (en) | 1997-01-09 | 1998-07-16 | Mitsui Chemicals, Inc. | Propylene polymer composition and thermoformed object |
| CA2277886A1 (en) | 1997-01-14 | 1998-07-16 | Dsm N.V. | A process for polymerizing olefins |
| NL1004992C2 (nl) | 1997-01-14 | 1998-07-15 | Dsm Nv | Toepassing van verbindingen die Si, Ge, Sn of Pb bevatten als cokatalysator bij de polymerisatie van olefinen. |
| FI970349A7 (fi) | 1997-01-28 | 1998-07-29 | Borealis As | Uudet metalloseeniyhdisteiden aktivaattorisysteemit |
| BR9807123A (pt) | 1997-01-29 | 2000-04-25 | Dow Chemical Co | Composições poliméricas heteromorfas, processo para sua obtenção e seus usos |
| US5798175A (en) | 1997-01-31 | 1998-08-25 | American Tape Company | Pressure sensitive adhesives and tape product prepared therefrom |
| US5827913A (en) | 1997-02-05 | 1998-10-27 | H.B. Fuller Licensing & Financing, Inc. | Hot melt adhesive comprising an encapsulated ingredient |
| US5739220A (en) | 1997-02-06 | 1998-04-14 | Fina Technology, Inc. | Method of olefin polymerization utilizing hydrogen pulsing, products made therefrom, and method of hydrogenation |
| CA2276214A1 (en) | 1997-02-07 | 1998-08-13 | Exxon Chemical Patents, Inc. | Preparation of vinyl-containing macromers |
| DE69809192T2 (de) * | 1997-02-07 | 2003-07-24 | Exxonmobil Chemical Patents Inc., Baytown | Propylenpolymere enthaltend polyethylenmakromonomere |
| ES2200314T3 (es) | 1997-02-07 | 2004-03-01 | Exxonmobil Chemical Patents Inc. | Copolimeros de olefina de procesamiento mejorado. |
| US6114457A (en) | 1997-02-07 | 2000-09-05 | Exxon Chemical Patents Inc. | High melt strength polyethylene compositions |
| US5756611A (en) | 1997-02-21 | 1998-05-26 | Lyondell Petrochemical Company | α-olefin polymerization catalysts |
| US5965477A (en) | 1997-02-21 | 1999-10-12 | Council Of Scientific & Industrial Research | Process for the preparation of supported metallocene catalyst |
| US6034164A (en) | 1997-02-21 | 2000-03-07 | Exxon Research And Engineering Co. | Nanocomposite materials formed from inorganic layered materials dispersed in a polymer matrix |
| US6451938B1 (en) | 1997-02-25 | 2002-09-17 | Exxon Mobil Chemical Patents Inc. | Polymerization catalyst system comprising heterocyclic fused cyclopentadienide ligands |
| CN1182292C (zh) | 1997-02-28 | 2004-12-29 | 肖氏工业集团有限公司 | 地毯、地毯背衬和使用均相支化乙烯聚合物制备地毯、地毯背衬的方法 |
| DE19709667A1 (de) | 1997-03-11 | 1998-09-17 | Basf Ag | Kammpolymere via Metallocenkatalyse |
| AU6463898A (en) | 1997-03-17 | 1998-10-12 | Exxon Chemical Patents Inc. | Transition metal metallacyclopentadienyl compounds |
| CA2200373C (en) | 1997-03-19 | 2005-11-15 | Rupert Edward Von Haken Spence | Heteroligand |
| US6080818A (en) | 1997-03-24 | 2000-06-27 | Huntsman Polymers Corporation | Polyolefin blends used for non-woven applications |
| AU702218B2 (en) | 1997-03-31 | 1999-02-18 | Kyushu-Taiyoukasei., Ltd. | Liner film for bulk container and container liner |
| US6255426B1 (en) | 1997-04-01 | 2001-07-03 | Exxon Chemical Patents, Inc. | Easy processing linear low density polyethylene |
| EP0975641A4 (en) | 1997-04-03 | 2003-03-12 | Univ Colorado State Res Found | POLYHALOGENED MONOHETEROBORANANION PREPARATIONS |
| SG67489A1 (en) * | 1997-04-07 | 1999-09-21 | Mitsui Chemicals Inc | Laminating propylene/1-butene random copolymer composition and composite film using the same |
| US6143683A (en) | 1997-04-09 | 2000-11-07 | Fina Technology, Inc. | Metallocene catalyst and catalyst system for polymerizing an olefin having at least 3 carbon atoms |
| DE19715155A1 (de) | 1997-04-11 | 1998-10-15 | Basf Ag | Katalysatorzubereitungen für die Herstellung von Olefin(co)polymeren |
| AR012582A1 (es) | 1997-04-14 | 2000-11-08 | Dow Global Technologies Inc | Composiciones polimericas de elongacion mejorada y formulaciones adhesivas de fusion en caliente que incluyen dicha composicion |
| TW420693B (en) | 1997-04-25 | 2001-02-01 | Mitsui Chemicals Inc | Olefin polymerization catalysts, transition metal compounds, and <alpha>-olefin/conjugated diene copolymers |
| CA2286683A1 (en) | 1997-04-29 | 1998-11-05 | The Dow Chemical Company | Amorphous propylene-polyene copolymers and compositions thereof |
| EP0977820B1 (en) * | 1997-04-30 | 2004-07-14 | Ato Findley Inc | Hot melt adhesive with high peel and shear strengths for nonwoven applications |
| EP0979074A4 (en) * | 1997-05-01 | 2003-07-09 | Novogen Inc | TREATMENT OR PREVENTION CLIMATE ACTION SYMPTOMS AND OSTEOPOROSIS |
| WO1998052686A1 (en) | 1997-05-22 | 1998-11-26 | Phillips Petroleum Company | Method for making and using a prepolymerized olefin polymerization catalyst |
| JP3458656B2 (ja) | 1997-05-27 | 2003-10-20 | 東ソー株式会社 | オレフィン重合用触媒およびオレフィン重合体の製造方法 |
| US5972510A (en) | 1997-06-05 | 1999-10-26 | Isis Innovation Limited | Spherulite particles of isotactic polypropylene |
| GB9712663D0 (en) | 1997-06-16 | 1997-08-20 | Borealis As | Process |
| FI972946L (fi) | 1997-07-11 | 1999-01-12 | Borealis As | Uudet metalloseeniyhdisteet etyleenisesti tyydyttämätt"mien monomeerien polymeroimiseksi |
| SG76545A1 (en) | 1997-07-11 | 2000-11-21 | Sumitomo Chemical Co | Propylene copolymer |
| DE19729833A1 (de) | 1997-07-11 | 1999-01-14 | Clariant Gmbh | Polypropylenwachs |
| KR20000068602A (ko) | 1997-07-22 | 2000-11-25 | 나까니시 히로유끼 | 에틸렌/α-올레핀 공중합체, 그 조성물 및, 공중합체 및 조성물 |
| ES2192788T3 (es) | 1997-07-28 | 2003-10-16 | Basell Polyolefin Gmbh | Procedimiento para la preparacion de metalocenos. |
| JP2001512127A (ja) | 1997-08-01 | 2001-08-21 | ザ ダウ ケミカル カンパニー | 触媒活性剤 |
| TR200000810T2 (tr) | 1997-08-27 | 2000-07-21 | The Dow Chemical Company | Polimerlerde çapraz bağlantı oluşturulması ve bu polimerlerin köpükleri |
| US6325956B2 (en) | 1997-08-27 | 2001-12-04 | The Dow Chemical Company | Crosslinking of polymers and foams thereof |
| US6019735A (en) | 1997-08-28 | 2000-02-01 | Visco Technologies, Inc. | Viscosity measuring apparatus and method of use |
| US6150297A (en) | 1997-09-15 | 2000-11-21 | The Dow Chemical Company | Cyclopentaphenanthrenyl metal complexes and polymerization process |
| US6909028B1 (en) | 1997-09-15 | 2005-06-21 | Kimberly-Clark Worldwide, Inc. | Stable breathable elastic garments |
| US6045900A (en) | 1997-09-15 | 2000-04-04 | Kimberly-Clark Worldwide, Inc. | Breathable filled film laminate |
| US5997981A (en) | 1997-09-15 | 1999-12-07 | Kimberly-Clark Worldwide, Inc. | Breathable barrier composite useful as an ideal loop fastener component |
| EP1019415A1 (en) | 1997-09-19 | 2000-07-19 | The Dow Chemical Company | Modified alumoxane catalyst activator |
| US6090325A (en) | 1997-09-24 | 2000-07-18 | Fina Technology, Inc. | Biaxially-oriented metallocene-based polypropylene films |
| DE19744102A1 (de) | 1997-10-06 | 1999-04-15 | Targor Gmbh | Katalysatorsystem |
| US5892079A (en) | 1997-10-17 | 1999-04-06 | Sri International | Metallocene catalysts and associated methods of preparation and use |
| US5986024A (en) | 1997-10-17 | 1999-11-16 | Sri International | Preparation of multimodal polymer compositions using multinuclear metallocene catalysts |
| JPH11115127A (ja) | 1997-10-17 | 1999-04-27 | Asahi Du Pont Flash Span Products Kk | 複合不織シート |
| WO1999020694A1 (en) | 1997-10-17 | 1999-04-29 | Huntsman Polymers Corporation | Novel polyolefins as blend component |
| US5990035A (en) | 1997-10-21 | 1999-11-23 | Koeppl; Alexander | Polymerization catalyst systems, their preparation, and use |
| WO1999020701A1 (en) | 1997-10-21 | 1999-04-29 | The Dow Chemical Company | Thermoplastic marking compositions |
| US6265512B1 (en) | 1997-10-23 | 2001-07-24 | 3M Innovative Company | Elastic polypropylenes and catalysts for their manufacture |
| WO1999024516A1 (en) | 1997-11-12 | 1999-05-20 | The Dow Chemical Company | Aqueous pressure sensitive adhesive formulations |
| US6551955B1 (en) | 1997-12-08 | 2003-04-22 | Albemarle Corporation | Particulate group 4 metallocene-aluminoxane catalyst compositions devoid of preformed support, and their preparation and their use |
| US6242545B1 (en) | 1997-12-08 | 2001-06-05 | Univation Technologies | Polymerization catalyst systems comprising substituted hafinocenes |
| US6677265B1 (en) | 1997-12-08 | 2004-01-13 | Albemarle Corporation | Process of producing self-supported catalysts |
| JP3403044B2 (ja) | 1997-12-09 | 2003-05-06 | キヤノン株式会社 | 包装容器 |
| US6184327B1 (en) | 1997-12-10 | 2001-02-06 | Exxon Chemical Patents, Inc. | Elastomeric propylene polymers |
| US6117962A (en) | 1997-12-10 | 2000-09-12 | Exxon Chemical Patents Inc. | Vinyl-containing stereospecific polypropylene macromers |
| US6197910B1 (en) * | 1997-12-10 | 2001-03-06 | Exxon Chemical Patents, Inc. | Propylene polymers incorporating macromers |
| US6069213A (en) * | 1997-12-16 | 2000-05-30 | Union Carbide Chemicals & Plastics Technology Corporation | Mixed catalyst system |
| US6277479B1 (en) | 1997-12-19 | 2001-08-21 | Kimberly-Clark Worldwide, Inc. | Microporous films having zoned breathability |
| DE69823230T2 (de) | 1997-12-23 | 2004-08-19 | The Dow Chemical Co., Midland | Nachbehandlung zur erhöhung des polymergehaltes in einem verfahren zur lösungspolymerisation von olefinen |
| US6042930A (en) * | 1997-12-24 | 2000-03-28 | The Dow Chemical Company | Plastic heat-activated adhesive labels |
| EP0931814A1 (en) * | 1998-01-21 | 1999-07-28 | Fina Research S.A. | Polyolefins and uses thereof |
| US6566467B1 (en) | 1998-01-22 | 2003-05-20 | Donald Frederick Lyons | Inhibitor composition for chloroprene polymerization |
| CA2228923A1 (en) | 1998-02-06 | 1999-08-06 | Nova Chemicals Ltd. | Process for preparing supported olefin polymerization catalyst |
| DE19806918A1 (de) * | 1998-02-19 | 1999-08-26 | Aventis Res & Tech Gmbh & Co | Katalysatorsystem, Verfahren zu seiner Herstellung und seine Verwendung zur Polymerisation von Olefinen |
| ATE243700T1 (de) | 1998-02-20 | 2003-07-15 | Dow Global Technologies Inc | Expandierte anionen enthaltende katalysatoraktivatoren |
| US6319998B1 (en) | 1998-03-04 | 2001-11-20 | Exxon Mobil Chemical Patents Inc. | Method for making polymer blends by using series reactors |
| US6262202B1 (en) * | 1998-03-04 | 2001-07-17 | Univation Technologies, Llc | Noncoordinating anions for olefin polymerization |
| IT1298616B1 (it) * | 1998-03-10 | 2000-01-12 | Enichem Spa | Complesso metallocenico pontato per la (co) polimerizzazione delle olefine |
| ATE236964T1 (de) | 1998-03-11 | 2003-04-15 | Dow Chemical Co | Verformbares druckempfindliches klebeband |
| KR20010041881A (ko) | 1998-03-16 | 2001-05-25 | 그래햄 이. 테일러 | 폴리올레핀 나노복합체 |
| DE19812229A1 (de) | 1998-03-20 | 1999-09-23 | Basf Ag | Polymere des Propens |
| US6281300B1 (en) | 1998-03-20 | 2001-08-28 | Exxon Chemical Patents, Inc. | Continuous slurry polymerization volatile removal |
| CN1295496A (zh) | 1998-03-26 | 2001-05-16 | 陶氏化学公司 | 离子交换过的硅酸铝－镁或氟化硅酸镁气凝胶及由其制备的催化剂载体 |
| WO1999050311A1 (en) | 1998-03-27 | 1999-10-07 | Exxon Chemical Patents Inc. | Polymeric supported catalysts for olefin polymerization |
| DE19813657A1 (de) | 1998-03-27 | 1999-09-30 | Aventis Res & Tech Gmbh & Co | Katalysatorsystem, Verfahren zu seiner Herstellung und seine Verwendung zur Polymerisation von Olefinen |
| JPH11310762A (ja) | 1998-04-17 | 1999-11-09 | Minnesota Mining & Mfg Co <3M> | 粘着剤組成物及びそれを使用した粘着剤製品 |
| JPH11302316A (ja) * | 1998-04-17 | 1999-11-02 | Tonen Corp | プロピレン共重合体の製造方法 |
| EP0953581B1 (en) | 1998-04-27 | 2004-01-07 | Repsol Quimica S.A. | Catalytic systems for the polymerization and copolymerization of alpha-olefins |
| KR100585546B1 (ko) | 1998-05-06 | 2006-05-30 | 헌츠만 폴리머스 코포레이션 | 보조촉매를 사용한 중합방법 |
| US6207606B1 (en) * | 1998-05-15 | 2001-03-27 | Univation Technologies, Llc | Mixed catalysts and their use in a polymerization process |
| US6709742B2 (en) | 1998-05-18 | 2004-03-23 | Dow Global Technologies Inc. | Crosslinked elastic fibers |
| BR9917674B1 (pt) | 1998-05-18 | 2012-06-12 | processo para produzir uma composiÇço de catalisador para polimerizar monâmeros. | |
| AR018359A1 (es) | 1998-05-18 | 2001-11-14 | Dow Global Technologies Inc | Articulo resistente al calor , configurado, irradiado y reticulado, libre de un agente de reticulacion de silano |
| EP1082353B1 (de) | 1998-05-23 | 2006-02-22 | Basell Polyolefine GmbH | Katalysatorsystem und seine verwendung zur polymerisation von propylen |
| US6177190B1 (en) * | 1998-05-29 | 2001-01-23 | 3M Innovative Properties Company | Radiation curable poly(1-alkene) based pressure-sensitive adhesives |
| AU4381199A (en) | 1998-06-16 | 2000-01-05 | Borealis Technology Oy | Olefin polymerization process |
| US6180229B1 (en) * | 1998-06-17 | 2001-01-30 | H. B. Fuller Licensing & Financing, Inc. | Hot melt pressure sensitive adhesive composition useful for contact coating on heat sensitive substrates |
| DE19827327A1 (de) | 1998-06-19 | 1999-12-30 | Targor Gmbh | Siegelbare Mehrschichtfolie aus einem Propen-Terpolymeren |
| DE69941036D1 (de) | 1998-06-25 | 2009-08-06 | Idemitsu Kosan Co | Propylenpolymer und Zusammensetzung damit, Formobjekt und Laminat damit sowie Verfahren zur Herstellung von Propylenpolymer und einer Zusammensetzung damit |
| MXPA00013015A (es) | 1998-06-30 | 2002-11-07 | Fuller H B Licensing Financ | Composicion adhesiva en caliente que comprende interpolimero de etileno homogeneo y copolimero de bloque. |
| WO2000001745A1 (en) | 1998-07-02 | 2000-01-13 | Exxon Chemical Patents Inc. | Propylene olefin copolymers |
| DE69935332T2 (de) | 1998-07-16 | 2007-10-31 | Univation Technologies, LLC, Houston | Lewis-säure cokatalysatoren auf aluminium-basis für die olefinpolymerisation |
| US6376416B1 (en) * | 1998-07-21 | 2002-04-23 | Japan Polychem Corporation | Olefin polymerization catalyst and process for producing olefin polymer |
| US5969217A (en) | 1998-07-23 | 1999-10-19 | Monsanto Corporation | Soybean cultivar 9380479521366 |
| EP1144533A3 (en) | 1998-07-30 | 2002-03-13 | The Dow Chemical Company | High temperature polyolefin based adhesive film with improved polarity for adhering to polyurethane foams |
| WO2000012572A1 (en) * | 1998-08-26 | 2000-03-09 | Exxon Chemical Patents Inc. | Branched polypropylene compositions |
| US6255414B1 (en) | 1998-09-01 | 2001-07-03 | E. I. Du Pont De Nemours And Company | Polymerization of olefins |
| EP0985677A1 (en) | 1998-09-07 | 2000-03-15 | Industrial Technology Research Institute | Dinuclear metallocene catalyst for olefin polymerization |
| US6177527B1 (en) * | 1998-09-08 | 2001-01-23 | Union Carbide Chemical & Plastics Technology Corporation | Process for the preparation of polyethylene or polypropylene |
| US6159888A (en) | 1998-09-09 | 2000-12-12 | Phillips Petroleum Company | Polymerization catalyst systems, their preparation, and use |
| US6124400A (en) | 1998-09-10 | 2000-09-26 | Academy Of Applied Science | Semicrystalline polymer alloy and process for preparation |
| US6121377A (en) | 1998-09-10 | 2000-09-19 | Academy Of Applied Science | Process for the production of thermoplastic elastomeric polyolefin alloys, including syndiotactic-atactic polypropylene alloys and isotactic-atactic polypropylene alloys, and catalysts therefore |
| US6221981B1 (en) * | 1998-09-14 | 2001-04-24 | Phillips Petroleum Company | Method for making and using a supported metallcene catalyst system |
| DE19903306A1 (de) | 1999-01-28 | 2000-08-03 | Targor Gmbh | Organometallverbindung, Katalysatorsystem enthaltend diese Organometallverbindung und seine Verwendung |
| KR100430438B1 (ko) | 1998-10-22 | 2004-07-19 | 대림산업 주식회사 | 담지메탈로센촉매,그제조방법및이를이용한폴리올레핀의중합방법 |
| US6300433B1 (en) | 1998-10-23 | 2001-10-09 | Exxonmobil Chemical Patents Inc. | Olefin copolymerization process with bridged hafnocenes |
| US6589892B1 (en) | 1998-11-13 | 2003-07-08 | Kimberly-Clark Worldwide, Inc. | Bicomponent nonwoven webs containing adhesive and a third component |
| US6281289B1 (en) | 1998-12-08 | 2001-08-28 | The Dow Chemical Company | Polypropylene/ethylene polymer fiber having improved bond performance and composition for making the same |
| US6258903B1 (en) | 1998-12-18 | 2001-07-10 | Univation Technologies | Mixed catalyst system |
| US6333389B2 (en) | 1998-12-18 | 2001-12-25 | Univation Technologies, Llc | Olefin polymerization catalysts, their production and use |
| KR100653018B1 (ko) | 1998-12-21 | 2006-11-30 | 엑손모빌 케미칼 패턴츠 인코포레이티드 | 분지형 반결정질 에틸렌-프로필렌 조성물 |
| WO2000039170A1 (en) | 1998-12-30 | 2000-07-06 | Union Carbide Chemicals & Plastics Technology Corporation | Compositions of preactivated unsupported catalyst having a given concentration and methods of using them |
| GB9902697D0 (en) | 1999-02-09 | 1999-03-31 | Bp Chem Int Ltd | Novel compounds |
| WO2000050466A1 (en) | 1999-02-22 | 2000-08-31 | Borealis Technology Oy | Olefin polymerisation process |
| US6545108B1 (en) | 1999-02-22 | 2003-04-08 | Eastman Chemical Company | Catalysts containing N-pyrrolyl substituted nitrogen donors |
| US6653254B1 (en) | 1999-02-22 | 2003-11-25 | Fina Technology, Inc | Ziegler-Natta catalyst with metallocene for olefin polymerization |
| US6620896B1 (en) | 1999-02-23 | 2003-09-16 | Eastman Chemical Company | Mixed olefin polymerization catalysts, processes employing such catalysts, and polymers obtained therefrom |
| GB9907154D0 (en) | 1999-03-29 | 1999-05-19 | Bp Chem Int Ltd | Polymerisation catalysts |
| WO2000059721A1 (en) | 1999-04-06 | 2000-10-12 | International Paper Company | Outdoor banner stock |
| US6127484A (en) | 1999-04-29 | 2000-10-03 | Equistar Chemicals, Lp | Olefin polymerization process |
| US6500563B1 (en) | 1999-05-13 | 2002-12-31 | Exxonmobil Chemical Patents Inc. | Elastic films including crystalline polymer and crystallizable polymers of propylene |
| GB9911245D0 (en) | 1999-05-15 | 1999-07-14 | Bp Chem Int Ltd | Polymerisation catalysts |
| US20010047065A1 (en) | 1999-06-03 | 2001-11-29 | Sun-Chueh Kao | Method for preparing a supported catalyst system and its use in a polymerization process |
| JP2001064322A (ja) | 1999-06-24 | 2001-03-13 | Idemitsu Petrochem Co Ltd | プロピレン系重合体及びその成形体並びにプロピレン系重合体の製造方法 |
| CA2377259A1 (en) | 1999-06-25 | 2001-01-04 | Randal Ray Ford | Process for the polymerization of olefins; polyolefins, and films and articles produced therefrom |
| US6657000B1 (en) | 1999-06-25 | 2003-12-02 | Kraton Polymers U.S. Llc | Hot melt pressure sensitive positioning adhesive (III) |
| US6207773B1 (en) * | 1999-07-28 | 2001-03-27 | Industrial Technology Research Institute | Metallocene catalyst for preparing olefin polymer |
| GB9917851D0 (en) | 1999-07-29 | 1999-09-29 | Borealis As | Process |
| DE19939078A1 (de) | 1999-08-18 | 2001-02-22 | Beiersdorf Ag | Verwendung von Isocyanaten bei der Herstellung von hochviskosen selbstklebenden Massen |
| DE19939071A1 (de) | 1999-08-18 | 2001-02-22 | Beiersdorf Ag | Verwendung von Schwefel und Schwefelspendern zur Vernetzung von hochviskosen selbstklebenden Schmelzhaftklebermassen basierend auf nicht thermoplastischen Elastomeren |
| DE19939074A1 (de) | 1999-08-18 | 2001-02-22 | Beiersdorf Ag | Verwendung von reaktiven Phenolharzen bei der Herstellung von hochviskosen selbstklebenden Massen |
| US6369176B1 (en) * | 1999-08-19 | 2002-04-09 | Dupont Dow Elastomers Llc | Process for preparing in a single reactor polymer blends having a broad molecular weight distribution |
| DE19940151A1 (de) | 1999-08-24 | 2001-03-01 | Targor Gmbh | Geträgerte Katalysatorsysteme, Verfahren zu ihrer Herstellung und Verfahren zur Herstellung von Poly-1-alkenen mit bimodaler oder multimodaler Molekularmassenverteilung |
| CN101195667A (zh) | 1999-08-31 | 2008-06-11 | 西湖朗维尤公司 | 聚烯烃生产方法 |
| US6639020B1 (en) | 1999-09-03 | 2003-10-28 | Exxon Mobil Chemical Patents Inc. | Plasticized polypropylene thermoplastics |
| US6287658B1 (en) | 1999-09-10 | 2001-09-11 | E. I. Du Pont De Nemours And Company | Flexible composite suitable as packaging material |
| SG82087A1 (en) * | 1999-09-10 | 2001-07-24 | Sumitomo Chemical Co | Pressure sensitive adhesive |
| US6183849B1 (en) | 1999-09-17 | 2001-02-06 | Exxon Research And Engineering Company | Method for manufacturing composite board using high oil content wax and the composite board made using high oil content wax |
| GB9923072D0 (en) | 1999-09-29 | 1999-12-01 | Bp Chem Int Ltd | Polymerisation catalyst |
| EP1218423B1 (en) | 1999-10-02 | 2005-03-16 | Borealis Technology Oy | Modified supported catalysts for the polymerization of olefins |
| BR0014609A (pt) | 1999-10-08 | 2002-06-11 | Procter & Gamble | Adesivos compreendendo polìmeros isotáticos, lineares |
| US6399722B1 (en) | 1999-12-01 | 2002-06-04 | Univation Technologies, Llc | Solution feed of multiple catalysts |
| AR023992A1 (es) | 1999-10-22 | 2002-09-04 | Univation Tech Llc | Metodos para introducir catalizadores multiples en un reactor en fase de gas o de suspension y un metodo para controlar un producto de polimerizacion producido usando dos o mas catalizadores |
| US6271323B1 (en) | 1999-10-28 | 2001-08-07 | Univation Technologies, Llc | Mixed catalyst compounds, catalyst systems and their use in a polymerization process |
| ES2216474T3 (es) | 1999-10-26 | 2004-10-16 | Repsol Quimica S.A. | Compuestos de bis cicoplentadienilo con enlaces de un solo carbono y complejos de metaloceno de los mismos. |
| WO2001030891A1 (en) | 1999-10-26 | 2001-05-03 | Idemitsu Petrochemical Co., Ltd. | Polypropylene film and multilayered laminate |
| US6559090B1 (en) | 1999-11-01 | 2003-05-06 | W. R. Grace & Co.-Conn. | Metallocene and constrained geometry catalyst systems employing agglomerated metal oxide/clay support-activator and method of their preparation |
| US6380327B1 (en) * | 1999-11-12 | 2002-04-30 | E. I. Du Pont De Nemours And Company | Chain transfer agents for olefin polymerization |
| US6340730B1 (en) | 1999-12-06 | 2002-01-22 | Univation Technologies, Llc | Multiple catalyst system |
| US20010053837A1 (en) | 1999-12-10 | 2001-12-20 | Agarwal Pawan Kumar | Articles formed from propylene diene copolymers |
| US6248832B1 (en) | 1999-12-10 | 2001-06-19 | Exxon Mobile Chemical Patents Inc. | Crosslinked blends of amorphous and crystalline polymers and their applications |
| US6323284B1 (en) | 1999-12-10 | 2001-11-27 | Exxonmobil Chemical Patents, Inc. | Method of preparation of crosslinked blends of amorphous and crystalline polymers |
| US20010007896A1 (en) | 1999-12-10 | 2001-07-12 | Agarwal Pawan Kumar | Propylene diene copolymers |
| BR0016286A (pt) | 1999-12-10 | 2002-08-27 | Exxon Chemical Patents Inc | Artigos formados a partir de copolìmeros de propileno dieno |
| CN1407995A (zh) | 1999-12-10 | 2003-04-02 | 埃克森化学专利公司 | 丙烯－二烯共聚的聚合物 |
| US20020013440A1 (en) | 1999-12-10 | 2002-01-31 | Agarwal Pawan Kumar | Propylene diene copolymers |
| US20010016639A1 (en) | 1999-12-10 | 2001-08-23 | Agarwal Pawan Kumar | Article formed from propylene diene copolymers |
| DE19960411B4 (de) | 1999-12-15 | 2005-09-15 | E.I. Du Pont De Nemours And Co., Wilmington | Verwendung eines Dispersionsklebstoffs als Kaschierkleber |
| US6750302B1 (en) | 1999-12-16 | 2004-06-15 | Phillips Petroleum Company | Organometal catalyst compositions |
| CN1222550C (zh) | 1999-12-21 | 2005-10-12 | 巴塞尔聚烯烃有限公司 | 用于制备双轴拉伸聚丙烯膜的半结晶丙烯聚合物组合物 |
| DE19962130A1 (de) | 1999-12-21 | 2001-07-05 | Basell Polypropylen Gmbh | Teilkristalline Propylenpolymerisat-Zusammensetzungen mit guter Eignung zur Herstellung von biaxial orientierten Folien |
| MXPA02006199A (es) | 1999-12-22 | 2003-10-15 | Exxon Chemical Patents Inc | Composiciones adhesivas a base de polipropileno. |
| BRPI0016723B1 (pt) | 1999-12-23 | 2018-02-27 | Basell Polyolefine Gmbh. | Metaloceno, sistema catalisador, e, processo para a copolimerização de propileno com etileno |
| US20020128401A1 (en) | 1999-12-28 | 2002-09-12 | Robert Charles Job | Self-supported hybrd catalysts for the production of polyolefins |
| US6444605B1 (en) | 1999-12-28 | 2002-09-03 | Union Carbide Chemicals & Plastics Technology Corporation | Mixed metal alkoxide and cycloalkadienyl catalysts for the production of polyolefins |
| US6403855B1 (en) | 1999-12-28 | 2002-06-11 | Exxon Mobil Chemical Patents Inc. | Synthesis of crystalline silicoaluminophosphates and use in olefin production |
| US6399531B1 (en) | 1999-12-28 | 2002-06-04 | Union Carbide Chemicals & Plastics Technology Corporation | Hybrid ziegler-natta and cycloalkadienyl catalysts for the production of polyolefins |
| US20020037979A1 (en) | 1999-12-28 | 2002-03-28 | Robert Charles Job | Mixed ziegler/metallocene catalysts for the production of bimodal polyolefins |
| DE19963585A1 (de) | 1999-12-29 | 2001-07-12 | Dupont Performance Coatings | Schmelzklebstoff-Zusammensetzung und Verfahren zum Verkleben von Substraten |
| US6329468B1 (en) | 2000-01-21 | 2001-12-11 | Bostik Findley, Inc. | Hot melt adhesive based on semicrystalline flexible polyolefins |
| KR100998236B1 (ko) | 2000-01-26 | 2010-12-06 | 미쓰이 가가쿠 가부시키가이샤 | 올레핀 중합체 및 그의 제조 방법 |
| US20020065192A1 (en) | 2000-02-18 | 2002-05-30 | Mackenzie Peter Borden | Productivity catalysts and microstructure control |
| US6579823B2 (en) | 2000-02-18 | 2003-06-17 | Eastman Chemical Company | Catalysts containing per-ortho aryl substituted aryl or heteroaryl substituted nitrogen donors |
| KR20020007419A (ko) | 2000-03-22 | 2002-01-26 | 간디 지오프레이 에이치. | 이소택틱 프로필렌 중합체 및 감소된 이소택틱성을 갖는유연성 프로필렌 중합체의 열가소성 조성물 및 그 제조방법 |
| IT1318436B1 (it) | 2000-03-31 | 2003-08-25 | Enichem Spa | Ciclopentadieni sostituiti policiclici e metodo per la loropreparazione. |
| AU2001244330A1 (en) | 2000-04-10 | 2001-10-23 | Bp Chemicals Limited | Polymerisation process |
| CA2388850A1 (en) | 2000-04-21 | 2001-11-01 | Exxonmobil Chemical Patents, Inc. | Process for spraying hot melt adhesives |
| US6528448B1 (en) | 2000-04-28 | 2003-03-04 | Phillips Petroleum Company | Polymerization catalyst compositions and processes to produce polymers and bimodal polymers |
| JP4938199B2 (ja) | 2000-06-14 | 2012-05-23 | 出光興産株式会社 | ポリオレフィン系ホットメルト接着剤用樹脂 |
| WO2001098381A2 (en) | 2000-06-16 | 2001-12-27 | Albemarle Corporation | Polymerization process using self-supported catalysts |
| US6376410B1 (en) * | 2000-06-30 | 2002-04-23 | Exxonmobil Chemical Patents Inc. | Metallocene compositions |
| US6380122B1 (en) | 2000-06-30 | 2002-04-30 | Exxonmobil Chemical Patents Inc. | Metallocene compositions |
| NO20013880L (no) | 2000-08-22 | 2002-02-25 | Rohm & Haas | Matriks og fremgangsmåte for fremstilling av polyolefiner |
| US6555238B2 (en) | 2000-08-24 | 2003-04-29 | Dupont-Toray Co. Ltd. | Polyimide film, method of manufacture, and metal interconnect board with polyimide film substrate |
| EP1201711A1 (en) * | 2000-10-27 | 2002-05-02 | ATOFINA Research | Polyethylene pipe resins and production thereof |
| US6489004B1 (en) | 2000-11-03 | 2002-12-03 | Kimberly-Clark Worldwide, Inc. | Hook and loop fastener having an increased coefficient of friction |
| US6489400B2 (en) | 2000-12-21 | 2002-12-03 | 3M Innovative Properties Company | Pressure-sensitive adhesive blends comprising ethylene/propylene-derived polymers and propylene-derived polymers and articles therefrom |
| US6657009B2 (en) | 2000-12-29 | 2003-12-02 | Kimberly-Clark Worldwide, Inc. | Hot-melt adhesive having improved bonding strength |
| US20020123538A1 (en) | 2000-12-29 | 2002-09-05 | Peiguang Zhou | Hot-melt adhesive based on blend of amorphous and crystalline polymers for multilayer bonding |
| US6774069B2 (en) | 2000-12-29 | 2004-08-10 | Kimberly-Clark Worldwide, Inc. | Hot-melt adhesive for non-woven elastic composite bonding |
| MY137183A (en) | 2001-03-16 | 2009-01-30 | Dow Global Technologies Inc | Method of making interpolymers and products made therefrom |
| FR2830868B1 (fr) | 2001-10-11 | 2004-12-03 | Atofina | Composition a base de polypropylene isotactique obtenu par catalyse metallocene et de polypropylene isotactique obtenu par catalyse ziegler natta, greffe |
| US6653385B2 (en) | 2001-10-18 | 2003-11-25 | Bostik Findley, Inc. | Hot melt adhesive composition based on a blend of amorphous poly-α-olefin and syndiotactic polypropylene |
| US20050159566A1 (en) | 2002-04-23 | 2005-07-21 | Idemitsu Kosan Co., Ltd | Process for producing highly flowable propylene polymer and highly flowable propylene polymer |
| EP1362870A1 (fr) * | 2002-05-16 | 2003-11-19 | Atofina | Structure multicouche comprenant un liant à base de polyoléfine greffée par un monomère acrylique |
| US7700707B2 (en) | 2002-10-15 | 2010-04-20 | Exxonmobil Chemical Patents Inc. | Polyolefin adhesive compositions and articles made therefrom |
| WO2004046214A2 (en) | 2002-10-15 | 2004-06-03 | Exxonmobil Chemical Patents Inc. | Multiple catalyst system for olefin polymerization and polymers produced therefrom |
| US7550528B2 (en) | 2002-10-15 | 2009-06-23 | Exxonmobil Chemical Patents Inc. | Functionalized olefin polymers |
| US7541402B2 (en) | 2002-10-15 | 2009-06-02 | Exxonmobil Chemical Patents Inc. | Blend functionalized polyolefin adhesive |
-
2004
- 2004-04-15 US US10/825,380 patent/US7223822B2/en not_active Expired - Lifetime
-
2005
- 2005-04-13 AT AT05777682T patent/ATE519795T1/de not_active IP Right Cessation
- 2005-04-13 JP JP2007508539A patent/JP5348732B2/ja not_active Expired - Fee Related
- 2005-04-13 WO PCT/US2005/012721 patent/WO2005113622A1/en not_active Ceased
- 2005-04-13 KR KR1020067023824A patent/KR101156777B1/ko not_active Expired - Fee Related
- 2005-04-13 EP EP05777682A patent/EP1753796B1/en not_active Expired - Lifetime
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10889662B2 (en) | 2014-12-12 | 2021-01-12 | Lg Chem, Ltd. | Metallocene-supported catalyst and method of preparing polyolefin using the same |
| US11767377B2 (en) | 2014-12-12 | 2023-09-26 | Lg Chem Ltd. | Metallocene-supported catalyst and method of preparing polyolefin using the same |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1753796A1 (en) | 2007-02-21 |
| KR20070015579A (ko) | 2007-02-05 |
| US20040220359A1 (en) | 2004-11-04 |
| ATE519795T1 (de) | 2011-08-15 |
| US7223822B2 (en) | 2007-05-29 |
| EP1753796B1 (en) | 2011-08-10 |
| KR101156777B1 (ko) | 2012-06-18 |
| CN101018815A (zh) | 2007-08-15 |
| JP2007532762A (ja) | 2007-11-15 |
| WO2005113622A1 (en) | 2005-12-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5348732B2 (ja) | オレフィン重合およびそれにより生成されるポリマーのための多種触媒および反応装置システム | |
| JP4972284B2 (ja) | オレフィン重合のための複数触媒系及びそれらから生成されたポリマー | |
| US7439312B2 (en) | Branched crystalline polypropylene | |
| CN1705688A (zh) | 用于烯烃聚合的多催化剂体系和由其生产的聚合物 | |
| US8143353B2 (en) | Polymerization process and adhesives therefrom | |
| US20040132935A1 (en) | Branched crystalline polypropylene | |
| WO2003070788A1 (fr) | Polymere de 1-butene a fluidite elevee et son procede de production | |
| US7662895B2 (en) | Syndiotactic propylene elastomers | |
| JP4847638B2 (ja) | プロピレン系樹脂組成物、その製造方法及び成形体 | |
| CN101018815B (zh) | 烯烃聚合用多催化剂和反应器系统及所生产的聚合物 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20080317 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20080414 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20080414 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20111206 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20120302 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20120619 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20120823 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20120830 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20121217 |
|
| TRDD | Decision of grant or rejection written | ||
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20130723 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20130819 |
|
| R150 | Certificate of patent or registration of utility model |
Ref document number: 5348732 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| LAPS | Cancellation because of no payment of annual fees |