CA2559576C - Catalyst composition comprising shuttling agent for ethylene multi-block copolymer formation - Google Patents
Catalyst composition comprising shuttling agent for ethylene multi-block copolymer formation Download PDFInfo
- Publication number
- CA2559576C CA2559576C CA2559576A CA2559576A CA2559576C CA 2559576 C CA2559576 C CA 2559576C CA 2559576 A CA2559576 A CA 2559576A CA 2559576 A CA2559576 A CA 2559576A CA 2559576 C CA2559576 C CA 2559576C
- Authority
- CA
- Canada
- Prior art keywords
- polymer
- catalyst
- ethylene
- block copolymer
- percent
- 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 294
- 239000000203 mixture Substances 0.000 title claims abstract description 248
- 239000003795 chemical substances by application Substances 0.000 title claims abstract description 149
- 229920001400 block copolymer Polymers 0.000 title claims abstract description 142
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 title claims description 151
- 239000005977 Ethylene Substances 0.000 title claims description 147
- 230000015572 biosynthetic process Effects 0.000 title description 23
- 229920000642 polymer Polymers 0.000 claims abstract description 564
- -1 metal complex olefin Chemical class 0.000 claims abstract description 232
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 120
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims abstract description 64
- 239000002685 polymerization catalyst Substances 0.000 claims abstract description 42
- 239000000126 substance Substances 0.000 claims abstract description 35
- 230000000704 physical effect Effects 0.000 claims abstract description 29
- 239000007795 chemical reaction product Substances 0.000 claims abstract description 21
- 238000000034 method Methods 0.000 claims description 181
- 239000000178 monomer Substances 0.000 claims description 111
- 230000008569 process Effects 0.000 claims description 105
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 94
- 229910052739 hydrogen Inorganic materials 0.000 claims description 75
- 229910052751 metal Inorganic materials 0.000 claims description 75
- 239000001257 hydrogen Substances 0.000 claims description 74
- 238000002844 melting Methods 0.000 claims description 73
- 230000008018 melting Effects 0.000 claims description 73
- 239000002184 metal Substances 0.000 claims description 73
- 239000000835 fiber Substances 0.000 claims description 69
- 150000001336 alkenes Chemical class 0.000 claims description 66
- 230000004927 fusion Effects 0.000 claims description 61
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 56
- 125000004429 atom Chemical group 0.000 claims description 54
- 239000003446 ligand Substances 0.000 claims description 50
- 150000001875 compounds Chemical class 0.000 claims description 42
- 125000000217 alkyl group Chemical group 0.000 claims description 41
- 238000002347 injection Methods 0.000 claims description 41
- 239000007924 injection Substances 0.000 claims description 41
- 238000007906 compression Methods 0.000 claims description 39
- 230000006835 compression Effects 0.000 claims description 39
- 239000004745 nonwoven fabric Substances 0.000 claims description 36
- 239000000853 adhesive Substances 0.000 claims description 35
- 230000001070 adhesive effect Effects 0.000 claims description 35
- 229910052757 nitrogen Inorganic materials 0.000 claims description 34
- 238000012546 transfer Methods 0.000 claims description 34
- 125000003118 aryl group Chemical group 0.000 claims description 33
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 32
- 238000003860 storage Methods 0.000 claims description 32
- 238000010348 incorporation Methods 0.000 claims description 28
- 230000007935 neutral effect Effects 0.000 claims description 27
- 238000004519 manufacturing process Methods 0.000 claims description 26
- 238000005299 abrasion Methods 0.000 claims description 25
- 125000000129 anionic group Chemical group 0.000 claims description 25
- 238000004458 analytical method Methods 0.000 claims description 20
- 150000007527 lewis bases Chemical class 0.000 claims description 20
- 229910052760 oxygen Inorganic materials 0.000 claims description 20
- 229910052782 aluminium Inorganic materials 0.000 claims description 19
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 18
- 239000001301 oxygen Chemical group 0.000 claims description 18
- 239000008188 pellet Substances 0.000 claims description 18
- 230000000903 blocking effect Effects 0.000 claims description 17
- 230000001186 cumulative effect Effects 0.000 claims description 17
- 230000000737 periodic effect Effects 0.000 claims description 17
- 239000002879 Lewis base Substances 0.000 claims description 16
- 125000005843 halogen group Chemical group 0.000 claims description 16
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical group [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 13
- 230000035515 penetration Effects 0.000 claims description 13
- 229910052698 phosphorus Chemical group 0.000 claims description 13
- 238000002360 preparation method Methods 0.000 claims description 13
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical group [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 12
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 12
- 239000011574 phosphorus Chemical group 0.000 claims description 12
- 230000003993 interaction Effects 0.000 claims description 10
- 238000000926 separation method Methods 0.000 claims description 9
- 229910052723 transition metal Inorganic materials 0.000 claims description 9
- 150000003624 transition metals Chemical class 0.000 claims description 9
- 125000004404 heteroalkyl group Chemical group 0.000 claims description 7
- 125000001072 heteroaryl group Chemical group 0.000 claims description 7
- 229920000089 Cyclic olefin copolymer Polymers 0.000 claims description 5
- 238000012644 addition polymerization Methods 0.000 claims description 5
- 230000009477 glass transition Effects 0.000 claims description 5
- 230000000930 thermomechanical effect Effects 0.000 claims description 5
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 4
- 239000011701 zinc Substances 0.000 claims description 4
- 239000012634 fragment Substances 0.000 claims description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 2
- 229910052725 zinc Inorganic materials 0.000 claims description 2
- 150000002259 gallium compounds Chemical class 0.000 claims 1
- 229920001577 copolymer Polymers 0.000 abstract description 89
- 239000010408 film Substances 0.000 description 101
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 87
- 230000000052 comparative effect Effects 0.000 description 71
- 239000010410 layer Substances 0.000 description 67
- 238000006243 chemical reaction Methods 0.000 description 66
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 62
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 57
- ZCBSOTLLNBJIEK-UHFFFAOYSA-N silane titanium Chemical compound [SiH4].[Ti] ZCBSOTLLNBJIEK-UHFFFAOYSA-N 0.000 description 54
- 238000007792 addition Methods 0.000 description 49
- 239000000523 sample Substances 0.000 description 44
- 238000000113 differential scanning calorimetry Methods 0.000 description 41
- 238000001938 differential scanning calorimetry curve Methods 0.000 description 41
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 39
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 39
- 239000000047 product Substances 0.000 description 37
- 238000009826 distribution Methods 0.000 description 36
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 30
- 239000007789 gas Substances 0.000 description 30
- 239000011521 glass Substances 0.000 description 29
- YSRFHVJGXPIDGR-UHFFFAOYSA-N dimethylsilane titanium Chemical compound [Ti].C[SiH2]C YSRFHVJGXPIDGR-UHFFFAOYSA-N 0.000 description 28
- 239000000243 solution Substances 0.000 description 28
- 229920001971 elastomer Polymers 0.000 description 27
- 125000000538 pentafluorophenyl group Chemical group FC1=C(F)C(F)=C(*)C(F)=C1F 0.000 description 27
- HQWPLXHWEZZGKY-UHFFFAOYSA-N diethylzinc Chemical compound CC[Zn]CC HQWPLXHWEZZGKY-UHFFFAOYSA-N 0.000 description 26
- 239000002904 solvent Substances 0.000 description 25
- 238000012360 testing method Methods 0.000 description 25
- JFLKFZNIIQFQBS-FNCQTZNRSA-N trans,trans-1,4-Diphenyl-1,3-butadiene Chemical compound C=1C=CC=CC=1\C=C\C=C\C1=CC=CC=C1 JFLKFZNIIQFQBS-FNCQTZNRSA-N 0.000 description 25
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 24
- 239000002245 particle Substances 0.000 description 24
- 229920002959 polymer blend Polymers 0.000 description 24
- 239000004743 Polypropylene Substances 0.000 description 23
- 239000003921 oil Substances 0.000 description 23
- 150000001450 anions Chemical class 0.000 description 22
- 125000004122 cyclic group Chemical group 0.000 description 22
- 230000000694 effects Effects 0.000 description 22
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 22
- 229920001155 polypropylene Polymers 0.000 description 22
- 229910052718 tin Inorganic materials 0.000 description 22
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 21
- 239000007788 liquid Substances 0.000 description 21
- 150000001993 dienes Chemical class 0.000 description 20
- 229910052735 hafnium Chemical group 0.000 description 20
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 19
- 150000001335 aliphatic alkanes Chemical class 0.000 description 18
- 239000000806 elastomer Substances 0.000 description 18
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 18
- 238000011084 recovery Methods 0.000 description 18
- 230000003213 activating effect Effects 0.000 description 17
- 239000012190 activator Substances 0.000 description 17
- 239000003963 antioxidant agent Substances 0.000 description 17
- 235000006708 antioxidants Nutrition 0.000 description 17
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 16
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 16
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 16
- 230000001976 improved effect Effects 0.000 description 16
- 238000002156 mixing Methods 0.000 description 16
- 239000010936 titanium Substances 0.000 description 16
- 229910052799 carbon Inorganic materials 0.000 description 15
- 230000002829 reductive effect Effects 0.000 description 15
- 229920001169 thermoplastic Polymers 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 14
- 125000003368 amide group Chemical group 0.000 description 14
- 229910052796 boron Inorganic materials 0.000 description 14
- 239000003085 diluting agent Substances 0.000 description 14
- ZSWFCLXCOIISFI-UHFFFAOYSA-N endo-cyclopentadiene Natural products C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 14
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical group [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 description 14
- 229920000098 polyolefin Polymers 0.000 description 14
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 14
- PBKONEOXTCPAFI-UHFFFAOYSA-N 1,2,4-trichlorobenzene Chemical compound ClC1=CC=C(Cl)C(Cl)=C1 PBKONEOXTCPAFI-UHFFFAOYSA-N 0.000 description 13
- 238000002474 experimental method Methods 0.000 description 13
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 13
- 230000006870 function Effects 0.000 description 13
- 125000005842 heteroatom Chemical group 0.000 description 13
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 13
- 229910052717 sulfur Inorganic materials 0.000 description 13
- 229910052726 zirconium Inorganic materials 0.000 description 13
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 12
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- 238000001816 cooling Methods 0.000 description 12
- 229920001198 elastomeric copolymer Polymers 0.000 description 12
- 239000006260 foam Substances 0.000 description 12
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 12
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 12
- 229920005604 random copolymer Polymers 0.000 description 12
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 11
- WBINWEFDUSTAQB-UHFFFAOYSA-N N-[[13-(difluoromethylidene)-4-tetracyclo[12.4.0.02,6.07,12]octadeca-1(18),2(6),3,7,9,11,14,16-octaenyl]methyl-oxosilyl]-N,2-dimethylpropan-2-amine titanium Chemical compound [Ti].C12=CC=CC=C2C(=C(F)F)C2=CC=CC=C2C2=C1CC(C[Si](=O)N(C)C(C)(C)C)=C2 WBINWEFDUSTAQB-UHFFFAOYSA-N 0.000 description 11
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 11
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 11
- 150000004696 coordination complex Chemical class 0.000 description 11
- 150000004820 halides Chemical class 0.000 description 11
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 11
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 11
- 239000002002 slurry Substances 0.000 description 11
- 239000011593 sulfur Substances 0.000 description 11
- 239000004416 thermosoftening plastic Substances 0.000 description 11
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical compound C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 description 10
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 10
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 10
- 150000001768 cations Chemical class 0.000 description 10
- 238000007334 copolymerization reaction Methods 0.000 description 10
- 238000004132 cross linking Methods 0.000 description 10
- 230000003647 oxidation Effects 0.000 description 10
- 238000007254 oxidation reaction Methods 0.000 description 10
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 10
- 239000007787 solid Substances 0.000 description 10
- 229910052719 titanium Inorganic materials 0.000 description 10
- 239000004793 Polystyrene Substances 0.000 description 9
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical group [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 9
- 239000000654 additive Substances 0.000 description 9
- 230000003078 antioxidant effect Effects 0.000 description 9
- 125000004432 carbon atom Chemical group C* 0.000 description 9
- 239000006229 carbon black Substances 0.000 description 9
- 235000019241 carbon black Nutrition 0.000 description 9
- 230000008030 elimination Effects 0.000 description 9
- 238000003379 elimination reaction Methods 0.000 description 9
- 238000001125 extrusion Methods 0.000 description 9
- 239000011159 matrix material Substances 0.000 description 9
- 239000000155 melt Substances 0.000 description 9
- 230000003287 optical effect Effects 0.000 description 9
- 229920000573 polyethylene Polymers 0.000 description 9
- 229920002223 polystyrene Polymers 0.000 description 9
- 238000012545 processing Methods 0.000 description 9
- 239000011541 reaction mixture Substances 0.000 description 9
- 230000009467 reduction Effects 0.000 description 9
- 239000005060 rubber Substances 0.000 description 9
- 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 9
- QWUWMCYKGHVNAV-UHFFFAOYSA-N 1,2-dihydrostilbene Chemical group C=1C=CC=CC=1CCC1=CC=CC=C1 QWUWMCYKGHVNAV-UHFFFAOYSA-N 0.000 description 8
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 8
- 239000002841 Lewis acid Substances 0.000 description 8
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 8
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical group [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 8
- 239000012986 chain transfer agent Substances 0.000 description 8
- 238000010924 continuous production Methods 0.000 description 8
- LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 description 8
- HEAMQYHBJQWOSS-UHFFFAOYSA-N ethene;oct-1-ene Chemical compound C=C.CCCCCCC=C HEAMQYHBJQWOSS-UHFFFAOYSA-N 0.000 description 8
- 229910052736 halogen Inorganic materials 0.000 description 8
- 150000002367 halogens Chemical class 0.000 description 8
- 150000007517 lewis acids Chemical class 0.000 description 8
- 238000000465 moulding Methods 0.000 description 8
- 239000012071 phase Substances 0.000 description 8
- 230000009257 reactivity Effects 0.000 description 8
- 239000000377 silicon dioxide Substances 0.000 description 8
- 229920002725 thermoplastic elastomer Polymers 0.000 description 8
- 239000004698 Polyethylene Substances 0.000 description 7
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 description 7
- 238000010828 elution Methods 0.000 description 7
- 229920001519 homopolymer Polymers 0.000 description 7
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 7
- 150000002978 peroxides Chemical class 0.000 description 7
- 230000002441 reversible effect Effects 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- 229920002397 thermoplastic olefin Polymers 0.000 description 7
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 7
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 6
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 6
- SDJHPPZKZZWAKF-UHFFFAOYSA-N 2,3-dimethylbuta-1,3-diene Chemical compound CC(=C)C(C)=C SDJHPPZKZZWAKF-UHFFFAOYSA-N 0.000 description 6
- AQZWEFBJYQSQEH-UHFFFAOYSA-N 2-methyloxaluminane Chemical compound C[Al]1CCCCO1 AQZWEFBJYQSQEH-UHFFFAOYSA-N 0.000 description 6
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 6
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 6
- 125000003545 alkoxy group Chemical group 0.000 description 6
- 230000003197 catalytic effect Effects 0.000 description 6
- 239000003153 chemical reaction reagent Substances 0.000 description 6
- JLTDJTHDQAWBAV-UHFFFAOYSA-O dimethyl(phenyl)azanium Chemical compound C[NH+](C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-O 0.000 description 6
- 238000010894 electron beam technology Methods 0.000 description 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 6
- 238000000605 extraction Methods 0.000 description 6
- 125000003800 germyl group Chemical group [H][Ge]([H])([H])[*] 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 150000002500 ions Chemical class 0.000 description 6
- SOEVKJXMZBAALG-UHFFFAOYSA-N octylalumane Chemical compound CCCCCCCC[AlH2] SOEVKJXMZBAALG-UHFFFAOYSA-N 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 125000001424 substituent group Chemical group 0.000 description 6
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 5
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 5
- 239000007983 Tris buffer Substances 0.000 description 5
- 150000001412 amines Chemical class 0.000 description 5
- 230000008859 change Effects 0.000 description 5
- 230000009977 dual effect Effects 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 238000012685 gas phase polymerization Methods 0.000 description 5
- 125000000592 heterocycloalkyl group Chemical group 0.000 description 5
- 239000002815 homogeneous catalyst Substances 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- 230000000670 limiting effect Effects 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- 150000002739 metals Chemical class 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 5
- JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 description 5
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 5
- 238000010926 purge Methods 0.000 description 5
- 150000003254 radicals Chemical class 0.000 description 5
- 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 4
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 description 4
- CPGFMWPQXUXQRX-UHFFFAOYSA-N 3-amino-3-(4-fluorophenyl)propanoic acid Chemical compound OC(=O)CC(N)C1=CC=C(F)C=C1 CPGFMWPQXUXQRX-UHFFFAOYSA-N 0.000 description 4
- 239000007848 Bronsted acid Substances 0.000 description 4
- 229920002943 EPDM rubber Polymers 0.000 description 4
- 238000005481 NMR spectroscopy Methods 0.000 description 4
- 235000021355 Stearic acid Nutrition 0.000 description 4
- 229910052775 Thulium Inorganic materials 0.000 description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 4
- 239000002671 adjuvant Substances 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 125000003342 alkenyl group Chemical group 0.000 description 4
- 238000010539 anionic addition polymerization reaction Methods 0.000 description 4
- 238000004630 atomic force microscopy Methods 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 230000002902 bimodal effect Effects 0.000 description 4
- 125000002091 cationic group Chemical group 0.000 description 4
- 238000013329 compounding Methods 0.000 description 4
- 238000002425 crystallisation Methods 0.000 description 4
- 230000008025 crystallization Effects 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
- MGDOJPNDRJNJBK-UHFFFAOYSA-N ethylaluminum Chemical compound [Al].C[CH2] MGDOJPNDRJNJBK-UHFFFAOYSA-N 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- 238000005194 fractionation Methods 0.000 description 4
- 239000002638 heterogeneous catalyst Substances 0.000 description 4
- 150000004678 hydrides Chemical class 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 238000003780 insertion Methods 0.000 description 4
- 230000037431 insertion Effects 0.000 description 4
- 238000011068 loading method Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 230000007246 mechanism Effects 0.000 description 4
- 150000002736 metal compounds Chemical class 0.000 description 4
- 150000002738 metalloids Chemical group 0.000 description 4
- 238000001000 micrograph Methods 0.000 description 4
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 4
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 4
- 125000002524 organometallic group Chemical group 0.000 description 4
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 4
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 4
- 125000003367 polycyclic group Chemical group 0.000 description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 4
- 238000010791 quenching Methods 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920006395 saturated elastomer Polymers 0.000 description 4
- 229910000077 silane Inorganic materials 0.000 description 4
- SCABQASLNUQUKD-UHFFFAOYSA-N silylium Chemical compound [SiH3+] SCABQASLNUQUKD-UHFFFAOYSA-N 0.000 description 4
- 241000894007 species Species 0.000 description 4
- 239000008117 stearic acid Substances 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- 229960002447 thiram Drugs 0.000 description 4
- 238000004073 vulcanization Methods 0.000 description 4
- 229940100888 zinc compound Drugs 0.000 description 4
- APPOKADJQUIAHP-GGWOSOGESA-N (2e,4e)-hexa-2,4-diene Chemical compound C\C=C\C=C\C APPOKADJQUIAHP-GGWOSOGESA-N 0.000 description 3
- PRBHEGAFLDMLAL-UHFFFAOYSA-N 1,5-Hexadiene Natural products CC=CCC=C PRBHEGAFLDMLAL-UHFFFAOYSA-N 0.000 description 3
- DJMUYABFXCIYSC-UHFFFAOYSA-N 1H-phosphole Chemical compound C=1C=CPC=1 DJMUYABFXCIYSC-UHFFFAOYSA-N 0.000 description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 239000004604 Blowing Agent Substances 0.000 description 3
- 239000004609 Impact Modifier Substances 0.000 description 3
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 3
- 239000006057 Non-nutritive feed additive Substances 0.000 description 3
- 239000004677 Nylon Substances 0.000 description 3
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 3
- 125000002877 alkyl aryl group Chemical group 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
- 150000001408 amides Chemical class 0.000 description 3
- 150000003863 ammonium salts Chemical class 0.000 description 3
- 125000003710 aryl alkyl group Chemical group 0.000 description 3
- 150000001540 azides Chemical class 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L calcium carbonate Substances [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 3
- 238000011088 calibration curve Methods 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 230000001419 dependent effect Effects 0.000 description 3
- 239000000539 dimer Substances 0.000 description 3
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 3
- 229910052732 germanium Inorganic materials 0.000 description 3
- PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical compound C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 3
- FFUAGWLWBBFQJT-UHFFFAOYSA-N hexamethyldisilazane Chemical compound C[Si](C)(C)N[Si](C)(C)C FFUAGWLWBBFQJT-UHFFFAOYSA-N 0.000 description 3
- 229920001903 high density polyethylene Polymers 0.000 description 3
- 239000004700 high-density polyethylene Substances 0.000 description 3
- 125000000743 hydrocarbylene group Chemical group 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- JBFYUZGYRGXSFL-UHFFFAOYSA-N imidazolide Chemical compound C1=C[N-]C=N1 JBFYUZGYRGXSFL-UHFFFAOYSA-N 0.000 description 3
- 150000002466 imines Chemical class 0.000 description 3
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 description 3
- 238000001746 injection moulding Methods 0.000 description 3
- 229910052747 lanthanoid Inorganic materials 0.000 description 3
- 150000002602 lanthanoids Chemical class 0.000 description 3
- 238000010550 living polymerization reaction Methods 0.000 description 3
- 229920002521 macromolecule Polymers 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
- JACMPVXHEARCBO-UHFFFAOYSA-N n-pentylpentan-1-amine Chemical compound CCCCCNCCCCC JACMPVXHEARCBO-UHFFFAOYSA-N 0.000 description 3
- 229920005615 natural polymer Polymers 0.000 description 3
- 229920001778 nylon Polymers 0.000 description 3
- 239000007800 oxidant agent Substances 0.000 description 3
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 3
- FVZVCSNXTFCBQU-UHFFFAOYSA-N phosphanyl Chemical group [PH2] FVZVCSNXTFCBQU-UHFFFAOYSA-N 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 3
- 239000004810 polytetrafluoroethylene Substances 0.000 description 3
- 239000012429 reaction media Substances 0.000 description 3
- 238000012216 screening Methods 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- 125000005374 siloxide group Chemical group 0.000 description 3
- 230000003068 static effect Effects 0.000 description 3
- 229920001059 synthetic polymer Polymers 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 3
- 235000010215 titanium dioxide Nutrition 0.000 description 3
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 3
- JLTRXTDYQLMHGR-UHFFFAOYSA-N trimethylaluminium Chemical group C[Al](C)C JLTRXTDYQLMHGR-UHFFFAOYSA-N 0.000 description 3
- LFXVBWRMVZPLFK-UHFFFAOYSA-N trioctylalumane Chemical compound CCCCCCCC[Al](CCCCCCCC)CCCCCCCC LFXVBWRMVZPLFK-UHFFFAOYSA-N 0.000 description 3
- POHPFVPVRKJHCR-UHFFFAOYSA-N tris(2,3,4,5,6-pentafluorophenyl)alumane Chemical group FC1=C(F)C(F)=C(F)C(F)=C1[Al](C=1C(=C(F)C(F)=C(F)C=1F)F)C1=C(F)C(F)=C(F)C(F)=C1F POHPFVPVRKJHCR-UHFFFAOYSA-N 0.000 description 3
- 150000003752 zinc compounds Chemical class 0.000 description 3
- 239000011787 zinc oxide Substances 0.000 description 3
- VPGLGRNSAYHXPY-UHFFFAOYSA-L zirconium(2+);dichloride Chemical compound Cl[Zr]Cl VPGLGRNSAYHXPY-UHFFFAOYSA-L 0.000 description 3
- OJOWICOBYCXEKR-APPZFPTMSA-N (1S,4R)-5-ethylidenebicyclo[2.2.1]hept-2-ene Chemical compound CC=C1C[C@@H]2C[C@@H]1C=C2 OJOWICOBYCXEKR-APPZFPTMSA-N 0.000 description 2
- PRBHEGAFLDMLAL-GQCTYLIASA-N (4e)-hexa-1,4-diene Chemical compound C\C=C\CC=C PRBHEGAFLDMLAL-GQCTYLIASA-N 0.000 description 2
- RELMFMZEBKVZJC-UHFFFAOYSA-N 1,2,3-trichlorobenzene Chemical compound ClC1=CC=CC(Cl)=C1Cl RELMFMZEBKVZJC-UHFFFAOYSA-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
- KOMNUTZXSVSERR-UHFFFAOYSA-N 1,3,5-tris(prop-2-enyl)-1,3,5-triazinane-2,4,6-trione Chemical compound C=CCN1C(=O)N(CC=C)C(=O)N(CC=C)C1=O KOMNUTZXSVSERR-UHFFFAOYSA-N 0.000 description 2
- XWJBRBSPAODJER-UHFFFAOYSA-N 1,7-octadiene Chemical compound C=CCCCCC=C XWJBRBSPAODJER-UHFFFAOYSA-N 0.000 description 2
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical compound CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 2
- GQEZCXVZFLOKMC-UHFFFAOYSA-N 1-hexadecene Chemical compound CCCCCCCCCCCCCCC=C GQEZCXVZFLOKMC-UHFFFAOYSA-N 0.000 description 2
- HFDVRLIODXPAHB-UHFFFAOYSA-N 1-tetradecene Chemical compound CCCCCCCCCCCCC=C HFDVRLIODXPAHB-UHFFFAOYSA-N 0.000 description 2
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 2
- 238000005160 1H NMR spectroscopy Methods 0.000 description 2
- BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 description 2
- GWYSGBSSRNFQBQ-UHFFFAOYSA-L 2,6-ditert-butylphenolate;octylaluminum(2+) Chemical compound CCCCCCCC[Al+2].CC(C)(C)C1=CC=CC(C(C)(C)C)=C1[O-].CC(C)(C)C1=CC=CC(C(C)(C)C)=C1[O-] GWYSGBSSRNFQBQ-UHFFFAOYSA-L 0.000 description 2
- CJSBUWDGPXGFGA-UHFFFAOYSA-N 4-methylpenta-1,3-diene Chemical compound CC(C)=CC=C CJSBUWDGPXGFGA-UHFFFAOYSA-N 0.000 description 2
- 125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- 239000004322 Butylated hydroxytoluene Substances 0.000 description 2
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 2
- VCFQUHAHCQJWKL-UHFFFAOYSA-N CC[Zn+].CC(C)(C)[O-] Chemical compound CC[Zn+].CC(C)(C)[O-] VCFQUHAHCQJWKL-UHFFFAOYSA-N 0.000 description 2
- RDRSMXYUSKJLIZ-UHFFFAOYSA-M CC[Zn+].[O-]C1=C(C=2C=CC=CC=2)C=CC=C1C1=CC=CC=C1 Chemical compound CC[Zn+].[O-]C1=C(C=2C=CC=CC=2)C=CC=C1C1=CC=CC=C1 RDRSMXYUSKJLIZ-UHFFFAOYSA-M 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- 229920000049 Carbon (fiber) Polymers 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- 239000004971 Cross linker Substances 0.000 description 2
- 239000004606 Fillers/Extenders Substances 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- XKCNCFRFJIKYMR-UHFFFAOYSA-N N,2-dimethyl-N-[(13-methylidene-3-tetracyclo[12.4.0.02,6.07,12]octadeca-1(18),2(6),4,7,9,11,14,16-octaenyl)methyl-oxosilyl]propan-2-amine titanium Chemical compound [Ti].C12=CC=CC=C2C(=C)C2=CC=CC=C2C2=C1C(C[Si](=O)N(C)C(C)(C)C)C=C2 XKCNCFRFJIKYMR-UHFFFAOYSA-N 0.000 description 2
- 241000183024 Populus tremula Species 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- 229910052581 Si3N4 Inorganic materials 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 2
- OKKRPWIIYQTPQF-UHFFFAOYSA-N Trimethylolpropane trimethacrylate Chemical compound CC(=C)C(=O)OCC(CC)(COC(=O)C(C)=C)COC(=O)C(C)=C OKKRPWIIYQTPQF-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 230000009102 absorption Effects 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 125000005234 alkyl aluminium group Chemical group 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 229910000091 aluminium hydride Inorganic materials 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 125000002178 anthracenyl group Chemical group C1(=CC=CC2=CC3=CC=CC=C3C=C12)* 0.000 description 2
- 125000004104 aryloxy group Chemical group 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 238000010923 batch production Methods 0.000 description 2
- ITKSXDXOEYKPIA-UHFFFAOYSA-N bis(trimethylsilyl)azanide;ethylaluminum(2+) Chemical compound CC[Al+2].C[Si](C)(C)[N-][Si](C)(C)C.C[Si](C)(C)[N-][Si](C)(C)C ITKSXDXOEYKPIA-UHFFFAOYSA-N 0.000 description 2
- 238000000071 blow moulding Methods 0.000 description 2
- 150000001639 boron compounds Chemical class 0.000 description 2
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 2
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 2
- 229940095259 butylated hydroxytoluene Drugs 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 238000004364 calculation method Methods 0.000 description 2
- 150000001721 carbon Chemical group 0.000 description 2
- 239000004917 carbon fiber Substances 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000012718 coordination polymerization Methods 0.000 description 2
- 239000011258 core-shell material Substances 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 125000004093 cyano group Chemical group *C#N 0.000 description 2
- 150000001925 cycloalkenes Chemical class 0.000 description 2
- MGNZXYYWBUKAII-UHFFFAOYSA-N cyclohexa-1,3-diene Chemical compound C1CC=CC=C1 MGNZXYYWBUKAII-UHFFFAOYSA-N 0.000 description 2
- 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 2
- BOXSCYUXSBYGRD-UHFFFAOYSA-N cyclopenta-1,3-diene;iron(3+) Chemical compound [Fe+3].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 BOXSCYUXSBYGRD-UHFFFAOYSA-N 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 229920003244 diene elastomer Polymers 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- QYHTVZBJWXQBDT-UHFFFAOYSA-J dizinc N,N-diethylcarbamodithioate Chemical compound [Zn++].[Zn++].CCN(CC)C([S-])=S.CCN(CC)C([S-])=S.CCN(CC)C([S-])=S.CCN(CC)C([S-])=S QYHTVZBJWXQBDT-UHFFFAOYSA-J 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- ZPGYSJMGYASTOM-UHFFFAOYSA-N ethyl(naphthalen-1-yl)azanide;octylaluminum(2+) Chemical compound CCCCCCCC[Al+2].C1=CC=C2C([N-]CC)=CC=CC2=C1.C1=CC=C2C([N-]CC)=CC=CC2=C1 ZPGYSJMGYASTOM-UHFFFAOYSA-N 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 238000009408 flooring Methods 0.000 description 2
- 238000005243 fluidization Methods 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 238000007306 functionalization reaction Methods 0.000 description 2
- 229910052733 gallium Inorganic materials 0.000 description 2
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N guanidine group Chemical group NC(=N)N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
- 150000002362 hafnium Chemical class 0.000 description 2
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical class C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- 229920000592 inorganic polymer Polymers 0.000 description 2
- 230000010354 integration Effects 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 239000004611 light stabiliser Substances 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 229920001684 low density polyethylene Polymers 0.000 description 2
- 239000004702 low-density polyethylene Substances 0.000 description 2
- 239000000395 magnesium oxide Substances 0.000 description 2
- 229910001507 metal halide Inorganic materials 0.000 description 2
- 150000005309 metal halides Chemical class 0.000 description 2
- 238000006263 metalation reaction Methods 0.000 description 2
- 229920001526 metallocene linear low density polyethylene Polymers 0.000 description 2
- 229910052752 metalloid Inorganic materials 0.000 description 2
- 239000010445 mica Substances 0.000 description 2
- 229910052618 mica group Inorganic materials 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- 229920006030 multiblock copolymer Polymers 0.000 description 2
- VAMFXQBUQXONLZ-UHFFFAOYSA-N n-alpha-eicosene Natural products CCCCCCCCCCCCCCCCCCC=C VAMFXQBUQXONLZ-UHFFFAOYSA-N 0.000 description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 239000002105 nanoparticle Substances 0.000 description 2
- 125000001624 naphthyl group Chemical group 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 150000002825 nitriles Chemical class 0.000 description 2
- 239000012299 nitrogen atmosphere Substances 0.000 description 2
- CCCMONHAUSKTEQ-UHFFFAOYSA-N octadec-1-ene Chemical compound CCCCCCCCCCCCCCCCC=C CCCMONHAUSKTEQ-UHFFFAOYSA-N 0.000 description 2
- 229920000620 organic polymer Polymers 0.000 description 2
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 2
- 229910052763 palladium Inorganic materials 0.000 description 2
- 239000010690 paraffinic oil Substances 0.000 description 2
- 230000036961 partial effect Effects 0.000 description 2
- QYZLKGVUSQXAMU-UHFFFAOYSA-N penta-1,4-diene Chemical compound C=CCC=C QYZLKGVUSQXAMU-UHFFFAOYSA-N 0.000 description 2
- 125000005062 perfluorophenyl group Chemical group FC1=C(C(=C(C(=C1F)F)F)F)* 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 230000000379 polymerizing effect Effects 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 229920001384 propylene homopolymer Polymers 0.000 description 2
- 230000001012 protector Effects 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 238000010526 radical polymerization reaction Methods 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 238000010058 rubber compounding Methods 0.000 description 2
- 229930195734 saturated hydrocarbon Natural products 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 238000012163 sequencing technique Methods 0.000 description 2
- 238000010008 shearing Methods 0.000 description 2
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 2
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 2
- 239000002356 single layer Substances 0.000 description 2
- 238000009987 spinning Methods 0.000 description 2
- 238000001694 spray drying Methods 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- 238000003856 thermoforming Methods 0.000 description 2
- 125000003944 tolyl group Chemical group 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- 125000005270 trialkylamine group Chemical group 0.000 description 2
- 229920000428 triblock copolymer Polymers 0.000 description 2
- SQBBHCOIQXKPHL-UHFFFAOYSA-N tributylalumane Chemical compound CCCC[Al](CCCC)CCCC SQBBHCOIQXKPHL-UHFFFAOYSA-N 0.000 description 2
- RGGPNXQUMRMPRA-UHFFFAOYSA-N triethylgallium Chemical compound CC[Ga](CC)CC RGGPNXQUMRMPRA-UHFFFAOYSA-N 0.000 description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
- ORYGRKHDLWYTKX-UHFFFAOYSA-N trihexylalumane Chemical compound CCCCCC[Al](CCCCCC)CCCCCC ORYGRKHDLWYTKX-UHFFFAOYSA-N 0.000 description 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 2
- CNWZYDSEVLFSMS-UHFFFAOYSA-N tripropylalumane Chemical compound CCC[Al](CCC)CCC CNWZYDSEVLFSMS-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- 239000002759 woven fabric Substances 0.000 description 2
- 239000010457 zeolite Substances 0.000 description 2
- BOXSVZNGTQTENJ-UHFFFAOYSA-L zinc dibutyldithiocarbamate Chemical compound [Zn+2].CCCCN(C([S-])=S)CCCC.CCCCN(C([S-])=S)CCCC BOXSVZNGTQTENJ-UHFFFAOYSA-L 0.000 description 2
- QXALIERKYGCHHA-UHFFFAOYSA-N (2,3,4,5,6-pentafluorophenyl)borane Chemical compound BC1=C(F)C(F)=C(F)C(F)=C1F QXALIERKYGCHHA-UHFFFAOYSA-N 0.000 description 1
- BOGRNZQRTNVZCZ-AATRIKPKSA-N (3e)-3-methylpenta-1,3-diene Chemical compound C\C=C(/C)C=C BOGRNZQRTNVZCZ-AATRIKPKSA-N 0.000 description 1
- AHAREKHAZNPPMI-AATRIKPKSA-N (3e)-hexa-1,3-diene Chemical compound CC\C=C\C=C AHAREKHAZNPPMI-AATRIKPKSA-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
- HFVZWWUGHWNHFL-FMIVXFBMSA-N (4e)-5,9-dimethyldeca-1,4,8-triene Chemical compound CC(C)=CCC\C(C)=C\CC=C HFVZWWUGHWNHFL-FMIVXFBMSA-N 0.000 description 1
- HYBLFDUGSBOMPI-BQYQJAHWSA-N (4e)-octa-1,4-diene Chemical compound CCC\C=C\CC=C HYBLFDUGSBOMPI-BQYQJAHWSA-N 0.000 description 1
- OJOWICOBYCXEKR-KRXBUXKQSA-N (5e)-5-ethylidenebicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(=C/C)/CC1C=C2 OJOWICOBYCXEKR-KRXBUXKQSA-N 0.000 description 1
- HITROERJXNWVOI-SOFGYWHQSA-N (5e)-octa-1,5-diene Chemical compound CC\C=C\CCC=C HITROERJXNWVOI-SOFGYWHQSA-N 0.000 description 1
- RJUCIROUEDJQIB-GQCTYLIASA-N (6e)-octa-1,6-diene Chemical compound C\C=C\CCCC=C RJUCIROUEDJQIB-GQCTYLIASA-N 0.000 description 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
- QVLAWKAXOMEXPM-DICFDUPASA-N 1,1,1,2-tetrachloro-2,2-dideuterioethane Chemical compound [2H]C([2H])(Cl)C(Cl)(Cl)Cl QVLAWKAXOMEXPM-DICFDUPASA-N 0.000 description 1
- BOGRNZQRTNVZCZ-UHFFFAOYSA-N 1,2-dimethyl-butadiene Natural products CC=C(C)C=C BOGRNZQRTNVZCZ-UHFFFAOYSA-N 0.000 description 1
- QTYUSOHYEPOHLV-FNORWQNLSA-N 1,3-Octadiene Chemical compound CCCC\C=C\C=C QTYUSOHYEPOHLV-FNORWQNLSA-N 0.000 description 1
- LEPPLSORKQWBNH-UHFFFAOYSA-N 1-(2-cyclopenta-2,4-dien-1-ylpropan-2-yl)-9H-fluorene Chemical compound C1(C=CC=C1)C(C)(C)C1=CC=CC=2C3=CC=CC=C3CC1=2 LEPPLSORKQWBNH-UHFFFAOYSA-N 0.000 description 1
- KTZVZZJJVJQZHV-UHFFFAOYSA-N 1-chloro-4-ethenylbenzene Chemical compound ClC1=CC=C(C=C)C=C1 KTZVZZJJVJQZHV-UHFFFAOYSA-N 0.000 description 1
- 229940106006 1-eicosene Drugs 0.000 description 1
- FIKTURVKRGQNQD-UHFFFAOYSA-N 1-eicosene Natural products CCCCCCCCCCCCCCCCCC=CC(O)=O FIKTURVKRGQNQD-UHFFFAOYSA-N 0.000 description 1
- VTPNYMSKBPZSTF-UHFFFAOYSA-N 1-ethenyl-2-ethylbenzene Chemical compound CCC1=CC=CC=C1C=C VTPNYMSKBPZSTF-UHFFFAOYSA-N 0.000 description 1
- NVZWEEGUWXZOKI-UHFFFAOYSA-N 1-ethenyl-2-methylbenzene Chemical compound CC1=CC=CC=C1C=C NVZWEEGUWXZOKI-UHFFFAOYSA-N 0.000 description 1
- XHUZSRRCICJJCN-UHFFFAOYSA-N 1-ethenyl-3-ethylbenzene Chemical compound CCC1=CC=CC(C=C)=C1 XHUZSRRCICJJCN-UHFFFAOYSA-N 0.000 description 1
- WHFHDVDXYKOSKI-UHFFFAOYSA-N 1-ethenyl-4-ethylbenzene Chemical compound CCC1=CC=C(C=C)C=C1 WHFHDVDXYKOSKI-UHFFFAOYSA-N 0.000 description 1
- CYXMOAZSOPXQOD-UHFFFAOYSA-N 1-methyl-2-(2-methylphenoxy)benzene Chemical compound CC1=CC=CC=C1OC1=CC=CC=C1C CYXMOAZSOPXQOD-UHFFFAOYSA-N 0.000 description 1
- BDAJBOIAMYRWFR-UHFFFAOYSA-N 1-methyl-2-(2-methylphenyl)sulfanylbenzene Chemical compound CC1=CC=CC=C1SC1=CC=CC=C1C BDAJBOIAMYRWFR-UHFFFAOYSA-N 0.000 description 1
- HBXWUCXDUUJDRB-UHFFFAOYSA-N 1-octadecoxyoctadecane Chemical compound CCCCCCCCCCCCCCCCCCOCCCCCCCCCCCCCCCCCC HBXWUCXDUUJDRB-UHFFFAOYSA-N 0.000 description 1
- WAUKBOOEPYNAGU-UHFFFAOYSA-N 1-phenylprop-2-enyl acetate Chemical compound CC(=O)OC(C=C)C1=CC=CC=C1 WAUKBOOEPYNAGU-UHFFFAOYSA-N 0.000 description 1
- ZMZGFLUUZLELNE-UHFFFAOYSA-N 2,3,5-triiodobenzoic acid Chemical compound OC(=O)C1=CC(I)=CC(I)=C1I ZMZGFLUUZLELNE-UHFFFAOYSA-N 0.000 description 1
- DKCPKDPYUFEZCP-UHFFFAOYSA-N 2,6-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=CC(C(C)(C)C)=C1O DKCPKDPYUFEZCP-UHFFFAOYSA-N 0.000 description 1
- ATGFTMUSEPZNJD-UHFFFAOYSA-N 2,6-diphenylphenol Chemical compound OC1=C(C=2C=CC=CC=2)C=CC=C1C1=CC=CC=C1 ATGFTMUSEPZNJD-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
- ICSNLGPSRYBMBD-UHFFFAOYSA-N 2-aminopyridine Chemical compound NC1=CC=CC=N1 ICSNLGPSRYBMBD-UHFFFAOYSA-N 0.000 description 1
- ISRGONDNXBCDBM-UHFFFAOYSA-N 2-chlorostyrene Chemical compound ClC1=CC=CC=C1C=C ISRGONDNXBCDBM-UHFFFAOYSA-N 0.000 description 1
- XUDBVJCTLZTSDC-UHFFFAOYSA-N 2-ethenylbenzoic acid Chemical compound OC(=O)C1=CC=CC=C1C=C XUDBVJCTLZTSDC-UHFFFAOYSA-N 0.000 description 1
- FZHNODDFDJBMAS-UHFFFAOYSA-N 2-ethoxyethenylbenzene Chemical compound CCOC=CC1=CC=CC=C1 FZHNODDFDJBMAS-UHFFFAOYSA-N 0.000 description 1
- WIWIYCUBSVLHGU-UHFFFAOYSA-N 2-heptadecyl-1H-imidazole tris(2,3,4,5,6-pentafluorophenyl)borane Chemical compound C(CCCCCCCCCCCCCCCC)C=1NC=CN1.FC1=C(C(=C(C(=C1B(C1=C(C(=C(C(=C1F)F)F)F)F)C1=C(C(=C(C(=C1F)F)F)F)F)F)F)F)F.FC1=C(C(=C(C(=C1B(C1=C(C(=C(C(=C1F)F)F)F)F)C1=C(C(=C(C(=C1F)F)F)F)F)F)F)F)F WIWIYCUBSVLHGU-UHFFFAOYSA-N 0.000 description 1
- CTHJQRHPNQEPAB-UHFFFAOYSA-N 2-methoxyethenylbenzene Chemical compound COC=CC1=CC=CC=C1 CTHJQRHPNQEPAB-UHFFFAOYSA-N 0.000 description 1
- FEUISMYEFPANSS-UHFFFAOYSA-N 2-methylcyclohexan-1-amine Chemical compound CC1CCCCC1N FEUISMYEFPANSS-UHFFFAOYSA-N 0.000 description 1
- MHGWNYIERCEISS-UHFFFAOYSA-N 2-methylpropyl(dioctadecyl)alumane Chemical compound CCCCCCCCCCCCCCCCCC[Al](CC(C)C)CCCCCCCCCCCCCCCCCC MHGWNYIERCEISS-UHFFFAOYSA-N 0.000 description 1
- XLLXMBCBJGATSP-UHFFFAOYSA-N 2-phenylethenol Chemical compound OC=CC1=CC=CC=C1 XLLXMBCBJGATSP-UHFFFAOYSA-N 0.000 description 1
- 125000000389 2-pyrrolyl group Chemical group [H]N1C([*])=C([H])C([H])=C1[H] 0.000 description 1
- IYIXYQPBHZBKMH-UHFFFAOYSA-N 2-sulfanyl-1,1-bis(sulfanylidene)-3H-1,3-benzothiazole-2-carboxylic acid Chemical compound C1=CC=C2S(=S)(=S)C(C(=O)O)(S)NC2=C1 IYIXYQPBHZBKMH-UHFFFAOYSA-N 0.000 description 1
- FDMFUZHCIRHGRG-UHFFFAOYSA-N 3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)C=C FDMFUZHCIRHGRG-UHFFFAOYSA-N 0.000 description 1
- RRIQVLZDOZPJTH-UHFFFAOYSA-N 3,5-di-tert-butyl-2-hydroxybenzaldehyde Chemical compound CC(C)(C)C1=CC(C=O)=C(O)C(C(C)(C)C)=C1 RRIQVLZDOZPJTH-UHFFFAOYSA-N 0.000 description 1
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 1
- YHQXBTXEYZIYOV-UHFFFAOYSA-N 3-methylbut-1-ene Chemical compound CC(C)C=C YHQXBTXEYZIYOV-UHFFFAOYSA-N 0.000 description 1
- LDTAOIUHUHHCMU-UHFFFAOYSA-N 3-methylpent-1-ene Chemical compound CCC(C)C=C LDTAOIUHUHHCMU-UHFFFAOYSA-N 0.000 description 1
- JGQBNAFULRKENS-UHFFFAOYSA-N 3H-pyridin-3-ylium-6-ylideneazanide Chemical group [N]C1=CC=CC=N1 JGQBNAFULRKENS-UHFFFAOYSA-N 0.000 description 1
- LPDGFTQFZFPTAU-UHFFFAOYSA-N 4,5-di(heptadecyl)-1H-imidazole tris(2,3,4,5,6-pentafluorophenyl)borane Chemical compound C(CCCCCCCCCCCCCCCC)C=1N=CNC1CCCCCCCCCCCCCCCCC.FC1=C(C(=C(C(=C1B(C1=C(C(=C(C(=C1F)F)F)F)F)C1=C(C(=C(C(=C1F)F)F)F)F)F)F)F)F.FC1=C(C(=C(C(=C1B(C1=C(C(=C(C(=C1F)F)F)F)F)C1=C(C(=C(C(=C1F)F)F)F)F)F)F)F)F LPDGFTQFZFPTAU-UHFFFAOYSA-N 0.000 description 1
- UBLAKNRDFHFPHO-UHFFFAOYSA-N 4,5-di(heptadecyl)-1h-imidazole;tris(2,3,4,5,6-pentafluorophenyl)alumane Chemical compound FC1=C(F)C(F)=C(F)C(F)=C1[Al](C=1C(=C(F)C(F)=C(F)C=1F)F)C1=C(F)C(F)=C(F)C(F)=C1F.FC1=C(F)C(F)=C(F)C(F)=C1[Al](C=1C(=C(F)C(F)=C(F)C=1F)F)C1=C(F)C(F)=C(F)C(F)=C1F.CCCCCCCCCCCCCCCCCC=1N=CNC=1CCCCCCCCCCCCCCCCC UBLAKNRDFHFPHO-UHFFFAOYSA-N 0.000 description 1
- TUPCVFAUMCDZQR-UHFFFAOYSA-N 4,5-di(heptadecyl)-4,5-dihydro-1h-imidazole;tris(2,3,4,5,6-pentafluorophenyl)alumane Chemical compound FC1=C(F)C(F)=C(F)C(F)=C1[Al](C=1C(=C(F)C(F)=C(F)C=1F)F)C1=C(F)C(F)=C(F)C(F)=C1F.FC1=C(F)C(F)=C(F)C(F)=C1[Al](C=1C(=C(F)C(F)=C(F)C=1F)F)C1=C(F)C(F)=C(F)C(F)=C1F.CCCCCCCCCCCCCCCCCC1NC=NC1CCCCCCCCCCCCCCCCC TUPCVFAUMCDZQR-UHFFFAOYSA-N 0.000 description 1
- NVMXZDYAGJNUHO-UHFFFAOYSA-N 4,5-di(heptadecyl)-4,5-dihydro-1h-imidazole;tris(2,3,4,5,6-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.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.CCCCCCCCCCCCCCCCCC1NC=NC1CCCCCCCCCCCCCCCCC NVMXZDYAGJNUHO-UHFFFAOYSA-N 0.000 description 1
- IMJNOGYDELWMCS-UHFFFAOYSA-N 4,5-di(undecyl)-1H-imidazole tris(2,3,4,5,6-pentafluorophenyl)borane Chemical compound C(CCCCCCCCCC)C=1N=CNC1CCCCCCCCCCC.FC1=C(C(=C(C(=C1B(C1=C(C(=C(C(=C1F)F)F)F)F)C1=C(C(=C(C(=C1F)F)F)F)F)F)F)F)F.FC1=C(C(=C(C(=C1B(C1=C(C(=C(C(=C1F)F)F)F)F)C1=C(C(=C(C(=C1F)F)F)F)F)F)F)F)F IMJNOGYDELWMCS-UHFFFAOYSA-N 0.000 description 1
- GLKJUVUPWZVQJL-UHFFFAOYSA-N 4,5-di(undecyl)-4,5-dihydro-1H-imidazole tris(2,3,4,5,6-pentafluorophenyl)alumane Chemical compound CCCCCCCCCCCC1NC=NC1CCCCCCCCCCC.FC1=C(F)C(F)=C(F)C(F)=C1[Al](C=1C(=C(F)C(F)=C(F)C=1F)F)C1=C(F)C(F)=C(F)C(F)=C1F.FC1=C(F)C(F)=C(F)C(F)=C1[Al](C=1C(=C(F)C(F)=C(F)C=1F)F)C1=C(F)C(F)=C(F)C(F)=C1F GLKJUVUPWZVQJL-UHFFFAOYSA-N 0.000 description 1
- DLLSFRXUQJKHBJ-UHFFFAOYSA-N 4,5-di(undecyl)-4,5-dihydro-1h-imidazole;tris(2,3,4,5,6-pentafluorophenyl)borane Chemical compound CCCCCCCCCCCC1NC=NC1CCCCCCCCCCC.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.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 DLLSFRXUQJKHBJ-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
- HBPSHRBTXIZBDI-UHFFFAOYSA-N 4-ethylidene-8-methylnona-1,7-diene Chemical compound C=CCC(=CC)CCC=C(C)C HBPSHRBTXIZBDI-UHFFFAOYSA-N 0.000 description 1
- NNYMYAMOJLOKMI-UHFFFAOYSA-N 5,6-dimethyl-1h-benzimidazole;tris(2,3,4,5,6-pentafluorophenyl)alumane Chemical compound C1=C(C)C(C)=CC2=C1NC=N2.FC1=C(F)C(F)=C(F)C(F)=C1[Al](C=1C(=C(F)C(F)=C(F)C=1F)F)C1=C(F)C(F)=C(F)C(F)=C1F.FC1=C(F)C(F)=C(F)C(F)=C1[Al](C=1C(=C(F)C(F)=C(F)C=1F)F)C1=C(F)C(F)=C(F)C(F)=C1F NNYMYAMOJLOKMI-UHFFFAOYSA-N 0.000 description 1
- QFUWXESVJSCLMD-UHFFFAOYSA-N 5-(2-cyclopenta-2,4-dien-1-ylethyl)cyclopenta-1,3-diene Chemical compound C1=CC=CC1CCC1C=CC=C1 QFUWXESVJSCLMD-UHFFFAOYSA-N 0.000 description 1
- TXQHJLUVWZNSLH-UHFFFAOYSA-N 5-ethenyl-2,5-dimethylcyclohexa-1,3-diene Chemical compound CC1(C=C)CC=C(C=C1)C TXQHJLUVWZNSLH-UHFFFAOYSA-N 0.000 description 1
- INYHZQLKOKTDAI-UHFFFAOYSA-N 5-ethenylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(C=C)CC1C=C2 INYHZQLKOKTDAI-UHFFFAOYSA-N 0.000 description 1
- PCBPVYHMZBWMAZ-UHFFFAOYSA-N 5-methylbicyclo[2.2.1]hept-2-ene Chemical compound C1C2C(C)CC1C=C2 PCBPVYHMZBWMAZ-UHFFFAOYSA-N 0.000 description 1
- QLKINISCYVCLTE-UHFFFAOYSA-N 6-phenylhexa-2,4-dienylbenzene Chemical compound C=1C=CC=CC=1CC=CC=CCC1=CC=CC=C1 QLKINISCYVCLTE-UHFFFAOYSA-N 0.000 description 1
- UCKITPBQPGXDHV-UHFFFAOYSA-N 7-methylocta-1,6-diene Chemical compound CC(C)=CCCCC=C UCKITPBQPGXDHV-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 241001556567 Acanthamoeba polyphaga mimivirus Species 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 239000004156 Azodicarbonamide Substances 0.000 description 1
- 229910000897 Babbitt (metal) Inorganic materials 0.000 description 1
- RKYBWUNRSUYSGB-UHFFFAOYSA-N C(CCCCCCCCCC)C1=CC2=C(N=CN2)C=C1CCCCCCCCCCC.FC1=C(C(=C(C(=C1B(C1=C(C(=C(C(=C1F)F)F)F)F)C1=C(C(=C(C(=C1F)F)F)F)F)F)F)F)F.FC1=C(C(=C(C(=C1B(C1=C(C(=C(C(=C1F)F)F)F)F)C1=C(C(=C(C(=C1F)F)F)F)F)F)F)F)F Chemical compound C(CCCCCCCCCC)C1=CC2=C(N=CN2)C=C1CCCCCCCCCCC.FC1=C(C(=C(C(=C1B(C1=C(C(=C(C(=C1F)F)F)F)F)C1=C(C(=C(C(=C1F)F)F)F)F)F)F)F)F.FC1=C(C(=C(C(=C1B(C1=C(C(=C(C(=C1F)F)F)F)F)C1=C(C(=C(C(=C1F)F)F)F)F)F)F)F)F RKYBWUNRSUYSGB-UHFFFAOYSA-N 0.000 description 1
- GZVCLWMMXROEKO-UHFFFAOYSA-N C(CCCCCCCCCC)C1=CC2=C(N=CN2)C=C1CCCCCCCCCCC.FC1=C(C(=C(C(=C1[Al](C1=C(C(=C(C(=C1F)F)F)F)F)C1=C(C(=C(C(=C1F)F)F)F)F)F)F)F)F.FC1=C(C(=C(C(=C1[Al](C1=C(C(=C(C(=C1F)F)F)F)F)C1=C(C(=C(C(=C1F)F)F)F)F)F)F)F)F Chemical compound C(CCCCCCCCCC)C1=CC2=C(N=CN2)C=C1CCCCCCCCCCC.FC1=C(C(=C(C(=C1[Al](C1=C(C(=C(C(=C1F)F)F)F)F)C1=C(C(=C(C(=C1F)F)F)F)F)F)F)F)F.FC1=C(C(=C(C(=C1[Al](C1=C(C(=C(C(=C1F)F)F)F)F)C1=C(C(=C(C(=C1F)F)F)F)F)F)F)F)F GZVCLWMMXROEKO-UHFFFAOYSA-N 0.000 description 1
- ODWQJTAVWQOFGZ-UHFFFAOYSA-N C(CCCCCCCCCCCCCCCC)C=1NCCN1.FC1=C(C(=C(C(=C1B(C1=C(C(=C(C(=C1F)F)F)F)F)C1=C(C(=C(C(=C1F)F)F)F)F)F)F)F)F.FC1=C(C(=C(C(=C1B(C1=C(C(=C(C(=C1F)F)F)F)F)C1=C(C(=C(C(=C1F)F)F)F)F)F)F)F)F Chemical compound C(CCCCCCCCCCCCCCCC)C=1NCCN1.FC1=C(C(=C(C(=C1B(C1=C(C(=C(C(=C1F)F)F)F)F)C1=C(C(=C(C(=C1F)F)F)F)F)F)F)F)F.FC1=C(C(=C(C(=C1B(C1=C(C(=C(C(=C1F)F)F)F)F)C1=C(C(=C(C(=C1F)F)F)F)F)F)F)F)F ODWQJTAVWQOFGZ-UHFFFAOYSA-N 0.000 description 1
- JAKYKQHNJUDFCT-UHFFFAOYSA-N C1=CC=C2C([Zr])C=CC2=C1 Chemical compound C1=CC=C2C([Zr])C=CC2=C1 JAKYKQHNJUDFCT-UHFFFAOYSA-N 0.000 description 1
- KFCDSBRUXVHFBC-UHFFFAOYSA-N C1C2=CC=CC=C2C(CCC2)=C1C2[Zr]([SiH](C)C)C1C(CC=2C3=CC=CC=2)=C3CCC1 Chemical compound C1C2=CC=CC=C2C(CCC2)=C1C2[Zr]([SiH](C)C)C1C(CC=2C3=CC=CC=2)=C3CCC1 KFCDSBRUXVHFBC-UHFFFAOYSA-N 0.000 description 1
- NOCXCDGSUBDFOX-UHFFFAOYSA-N C=1C=CC=CC=1C=CC=CC1=CC=CC=C1.CC1=CC2=CC=CC=C2C1[Zr]([SiH](C)C)C1C2=CC=CC=C2C=C1C Chemical compound C=1C=CC=CC=1C=CC=CC1=CC=CC=C1.CC1=CC2=CC=CC=C2C1[Zr]([SiH](C)C)C1C2=CC=CC=C2C=C1C NOCXCDGSUBDFOX-UHFFFAOYSA-N 0.000 description 1
- CZWJHDSWZZDHNY-UHFFFAOYSA-N CC1=C(C(=C(C1C(C)(C)C1C(=C(C(=C1C)C)C)C)C)C)C Chemical compound CC1=C(C(=C(C1C(C)(C)C1C(=C(C(=C1C)C)C)C)C)C)C CZWJHDSWZZDHNY-UHFFFAOYSA-N 0.000 description 1
- DQUAINJPECZAKA-UHFFFAOYSA-L CCCCC1=CC(C=C1)[Zr](Cl)(Cl)(C1C=CC(CCCC)=C1)[SiH](C)C Chemical compound CCCCC1=CC(C=C1)[Zr](Cl)(Cl)(C1C=CC(CCCC)=C1)[SiH](C)C DQUAINJPECZAKA-UHFFFAOYSA-L 0.000 description 1
- VQSJPZNVOGMWDC-UHFFFAOYSA-N CCCCCCCCCCCC1=C(CCCCCCCCCCC)N=CN1.FC(C(F)=C(C([Al](C(C(F)=C(C(F)=C1F)F)=C1F)C(C(F)=C(C(F)=C1F)F)=C1F)=C1F)F)=C1F.FC(C(F)=C(C([Al](C(C(F)=C(C(F)=C1F)F)=C1F)C(C(F)=C(C(F)=C1F)F)=C1F)=C1F)F)=C1F Chemical compound CCCCCCCCCCCC1=C(CCCCCCCCCCC)N=CN1.FC(C(F)=C(C([Al](C(C(F)=C(C(F)=C1F)F)=C1F)C(C(F)=C(C(F)=C1F)F)=C1F)=C1F)F)=C1F.FC(C(F)=C(C([Al](C(C(F)=C(C(F)=C1F)F)=C1F)C(C(F)=C(C(F)=C1F)F)=C1F)=C1F)F)=C1F VQSJPZNVOGMWDC-UHFFFAOYSA-N 0.000 description 1
- IPNXHVRSEMKUBA-UHFFFAOYSA-N CCCCCCCCCCCCCCCCCC1=NC=CN1.FC(C(F)=C(C([Al](C(C(F)=C(C(F)=C1F)F)=C1F)C(C(F)=C(C(F)=C1F)F)=C1F)=C1F)F)=C1F.FC(C(F)=C(C([Al](C(C(F)=C(C(F)=C1F)F)=C1F)C(C(F)=C(C(F)=C1F)F)=C1F)=C1F)F)=C1F Chemical compound CCCCCCCCCCCCCCCCCC1=NC=CN1.FC(C(F)=C(C([Al](C(C(F)=C(C(F)=C1F)F)=C1F)C(C(F)=C(C(F)=C1F)F)=C1F)=C1F)F)=C1F.FC(C(F)=C(C([Al](C(C(F)=C(C(F)=C1F)F)=C1F)C(C(F)=C(C(F)=C1F)F)=C1F)=C1F)F)=C1F IPNXHVRSEMKUBA-UHFFFAOYSA-N 0.000 description 1
- UQTVWGHDJHVLEP-UHFFFAOYSA-N CCCC[Zn]CCCC Chemical compound CCCC[Zn]CCCC UQTVWGHDJHVLEP-UHFFFAOYSA-N 0.000 description 1
- BPMGYFSWCJZSBA-UHFFFAOYSA-N C[SiH](C)O[SiH3] Chemical compound C[SiH](C)O[SiH3] BPMGYFSWCJZSBA-UHFFFAOYSA-N 0.000 description 1
- MCQZZZFXUGBKDA-UHFFFAOYSA-N C[SiH](C)[Ti](C1(C(=C(C(=C1)C)C)C)C)C1(C(=C(C(=C1)C)C)C)C Chemical compound C[SiH](C)[Ti](C1(C(=C(C(=C1)C)C)C)C)C1(C(=C(C(=C1)C)C)C)C MCQZZZFXUGBKDA-UHFFFAOYSA-N 0.000 description 1
- YYOHSEOBMBTBOR-UHFFFAOYSA-L C[SiH](C)[Zr](Cl)(Cl)(C1C=CC=C1C(C)(C)C)C1C=CC=C1C(C)(C)C Chemical compound C[SiH](C)[Zr](Cl)(Cl)(C1C=CC=C1C(C)(C)C)C1C=CC=C1C(C)(C)C YYOHSEOBMBTBOR-UHFFFAOYSA-L 0.000 description 1
- VWOTWOPAYZNLIU-UHFFFAOYSA-L C[SiH]C.Cl[Zr](Cl)(C1C=CC=C1)C1C=CC=C1 Chemical compound C[SiH]C.Cl[Zr](Cl)(C1C=CC=C1)C1C=CC=C1 VWOTWOPAYZNLIU-UHFFFAOYSA-L 0.000 description 1
- MZZLCYTXLHHGSK-UHFFFAOYSA-N C[Si](C1CCCC=2C3=CC=CC=C3CC1=2)(C1C=CC=C1)C Chemical compound C[Si](C1CCCC=2C3=CC=CC=C3CC1=2)(C1C=CC=C1)C MZZLCYTXLHHGSK-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical class [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 1
- 239000004831 Hot glue Substances 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- 229920002633 Kraton (polymer) Polymers 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 239000004594 Masterbatch (MB) Substances 0.000 description 1
- LIMUYEVEOUTWQS-UHFFFAOYSA-N N,2-dimethyl-N-[(13-methylidene-3-tetracyclo[12.4.0.02,6.07,12]octadeca-1(18),2(6),4,7,9,11,14,16-octaenyl)methyl-oxosilyl]propan-2-amine penta-1,3-diene titanium(2+) Chemical compound [Ti+2].CC=CC=C.C12=CC=CC=C2C(=C)C2=CC=CC=C2C2=C1C(C[Si](=O)N(C)C(C)(C)C)C=C2 LIMUYEVEOUTWQS-UHFFFAOYSA-N 0.000 description 1
- OQWSUZBBRRDKSY-UHFFFAOYSA-L N,2-dimethyl-N-[(13-methylidene-3-tetracyclo[12.4.0.02,6.07,12]octadeca-1(18),2(6),4,7,9,11,14,16-octaenyl)methyl-oxosilyl]propan-2-amine titanium(4+) dichloride Chemical compound [Cl-].[Cl-].[Ti+4].C12=CC=CC=C2C(=C)C2=CC=CC=C2C2=C1C(C[Si](=O)N(C)C(C)(C)C)C=C2 OQWSUZBBRRDKSY-UHFFFAOYSA-L 0.000 description 1
- ONFZORCVGBGSAC-UHFFFAOYSA-N N,2-dimethyl-N-[(13-methylidene-4-tetracyclo[12.4.0.02,6.07,12]octadeca-1(18),2(6),3,7,9,11,14,16-octaenyl)methyl-oxosilyl]propan-2-amine penta-1,3-diene titanium(2+) Chemical compound [Ti+2].CC=CC=C.C12=CC=CC=C2C(=C)C2=CC=CC=C2C2=C1CC(C[Si](=O)N(C)C(C)(C)C)=C2 ONFZORCVGBGSAC-UHFFFAOYSA-N 0.000 description 1
- ONQZBLLDLGDXSF-UHFFFAOYSA-N N,2-dimethyl-N-[(13-methylidene-4-tetracyclo[12.4.0.02,6.07,12]octadeca-1(18),2(6),3,7,9,11,14,16-octaenyl)methyl-oxosilyl]propan-2-amine titanium(3+) Chemical compound [Ti+3].C12=CC=CC=C2C(=C)C2=CC=CC=C2C2=C1CC(C[Si](=O)N(C)C(C)(C)C)=C2 ONQZBLLDLGDXSF-UHFFFAOYSA-N 0.000 description 1
- YUEWPIOZDIYXAK-UHFFFAOYSA-L N,2-dimethyl-N-[(13-methylidene-4-tetracyclo[12.4.0.02,6.07,12]octadeca-1(18),2(6),3,7,9,11,14,16-octaenyl)methyl-oxosilyl]propan-2-amine titanium(4+) dichloride Chemical compound [Cl-].[Cl-].[Ti+4].C12=CC=CC=C2C(=C)C2=CC=CC=C2C2=C1CC(C[Si](=O)N(C)C(C)(C)C)=C2 YUEWPIOZDIYXAK-UHFFFAOYSA-L 0.000 description 1
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 1
- ZKWHDXLPSZEWJP-UHFFFAOYSA-N N-[[13-(difluoromethylidene)-3-tetracyclo[12.4.0.02,6.07,12]octadeca-1(18),2(6),4,7,9,11,14,16-octaenyl]methyl-oxosilyl]-N,2-dimethylpropan-2-amine 4-phenylbuta-1,3-dienylbenzene titanium(2+) Chemical compound [Ti+2].C=1C=CC=CC=1C=CC=CC1=CC=CC=C1.C12=CC=CC=C2C(=C(F)F)C2=CC=CC=C2C2=C1C(C[Si](=O)N(C)C(C)(C)C)C=C2 ZKWHDXLPSZEWJP-UHFFFAOYSA-N 0.000 description 1
- ZTUMBFSBFBKZKN-UHFFFAOYSA-N N-[[13-(difluoromethylidene)-4-tetracyclo[12.4.0.02,6.07,12]octadeca-1(18),2(6),3,7,9,11,14,16-octaenyl]methyl-oxosilyl]-N,2-dimethylpropan-2-amine penta-1,3-diene titanium(2+) Chemical compound [Ti+2].CC=CC=C.C12=CC=CC=C2C(=C(F)F)C2=CC=CC=C2C2=C1CC(C[Si](=O)N(C)C(C)(C)C)=C2 ZTUMBFSBFBKZKN-UHFFFAOYSA-N 0.000 description 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 1
- 229910052779 Neodymium Inorganic materials 0.000 description 1
- 241000143392 Oar Species 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 1
- 229920000034 Plastomer Polymers 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 1
- 229910052771 Terbium Inorganic materials 0.000 description 1
- 241001122767 Theaceae Species 0.000 description 1
- 239000004433 Thermoplastic polyurethane Substances 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- SWMVJOXVIGSMEN-OUKQBFOZSA-N [(1e)-3-phenylbuta-1,3-dienyl]benzene Chemical compound C=1C=CC=CC=1C(=C)\C=C\C1=CC=CC=C1 SWMVJOXVIGSMEN-OUKQBFOZSA-N 0.000 description 1
- NAQHQEGMBKTRDE-UHFFFAOYSA-L [Cl-].[Cl-].C1=CC(CCCC2)=C2C1[Zr+2]([SiH](C)C)C1C(CCCC2)=C2C=C1 Chemical compound [Cl-].[Cl-].C1=CC(CCCC2)=C2C1[Zr+2]([SiH](C)C)C1C(CCCC2)=C2C=C1 NAQHQEGMBKTRDE-UHFFFAOYSA-L 0.000 description 1
- 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 1
- SFQHGFKMDOOMPT-UHFFFAOYSA-L [Cl-].[Cl-].[Ti+4].C12=CC=CC=C2C(=C(F)F)C2=CC=CC=C2C2=C1C(C[Si](=O)N(C)C(C)(C)C)C=C2 Chemical compound [Cl-].[Cl-].[Ti+4].C12=CC=CC=C2C(=C(F)F)C2=CC=CC=C2C2=C1C(C[Si](=O)N(C)C(C)(C)C)C=C2 SFQHGFKMDOOMPT-UHFFFAOYSA-L 0.000 description 1
- GBGURCGKYGCOQE-UHFFFAOYSA-N [Ti+2].C=1C=CC=CC=1C=CC=CC1=CC=CC=C1.C12=CC=CC=C2C(=C)C2=CC=CC=C2C2=C1CC(C[Si](=O)N(C)C(C)(C)C)=C2 Chemical compound [Ti+2].C=1C=CC=CC=1C=CC=CC1=CC=CC=C1.C12=CC=CC=C2C(=C)C2=CC=CC=C2C2=C1CC(C[Si](=O)N(C)C(C)(C)C)=C2 GBGURCGKYGCOQE-UHFFFAOYSA-N 0.000 description 1
- YBLVIQXVVYTYAE-UHFFFAOYSA-N [Ti+2].CC=CC=C.C12=CC=CC=C2C(=C(F)F)C2=CC=CC=C2C2=C1C(C[Si](=O)N(C)C(C)(C)C)C=C2 Chemical compound [Ti+2].CC=CC=C.C12=CC=CC=C2C(=C(F)F)C2=CC=CC=C2C2=C1C(C[Si](=O)N(C)C(C)(C)C)C=C2 YBLVIQXVVYTYAE-UHFFFAOYSA-N 0.000 description 1
- YIERUBIZXGKGJD-UHFFFAOYSA-N [Ti+3].C12=CC=CC=C2C(=C(F)F)C2=CC=CC=C2C2=C1C(C[Si](=O)N(C)C(C)(C)C)C=C2 Chemical compound [Ti+3].C12=CC=CC=C2C(=C(F)F)C2=CC=CC=C2C2=C1C(C[Si](=O)N(C)C(C)(C)C)C=C2 YIERUBIZXGKGJD-UHFFFAOYSA-N 0.000 description 1
- OCAGVJWIPGWEGO-UHFFFAOYSA-N [Ti+3].C12=CC=CC=C2C(=C)C2=CC=CC=C2C2=C1C(C[Si](=O)N(C)C(C)(C)C)C=C2 Chemical compound [Ti+3].C12=CC=CC=C2C(=C)C2=CC=CC=C2C2=C1C(C[Si](=O)N(C)C(C)(C)C)C=C2 OCAGVJWIPGWEGO-UHFFFAOYSA-N 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000004703 alkoxides Chemical class 0.000 description 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
- 125000004414 alkyl thio group Chemical group 0.000 description 1
- 125000005529 alkyleneoxy group Chemical group 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 238000005576 amination reaction Methods 0.000 description 1
- 229920006125 amorphous polymer Polymers 0.000 description 1
- 230000009118 appropriate response Effects 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 125000006615 aromatic heterocyclic group Chemical group 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical group 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- 125000005161 aryl oxy carbonyl group Chemical group 0.000 description 1
- 125000000732 arylene group Chemical group 0.000 description 1
- 229920001585 atactic polymer Polymers 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 description 1
- 235000019399 azodicarbonamide Nutrition 0.000 description 1
- 125000003112 azulen-2-yl group Chemical group [H]C1=C2C([H])=C([H])C([H])=C([H])C([H])=C2C([H])=C1* 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- KLTWGRFNJPLFDA-UHFFFAOYSA-N benzimidazolide Chemical class C1=CC=C2[N-]C=NC2=C1 KLTWGRFNJPLFDA-UHFFFAOYSA-N 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 229910002056 binary alloy Inorganic materials 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- IFVTZJHWGZSXFD-UHFFFAOYSA-N biphenylene Chemical group C1=CC=C2C3=CC=CC=C3C2=C1 IFVTZJHWGZSXFD-UHFFFAOYSA-N 0.000 description 1
- DXYTUIWIDDBVLU-UHFFFAOYSA-N bis(1h-inden-1-yl)-dimethylsilane Chemical compound C1=CC2=CC=CC=C2C1[Si](C)(C)C1C2=CC=CC=C2C=C1 DXYTUIWIDDBVLU-UHFFFAOYSA-N 0.000 description 1
- WPULPXOJFCAWLF-UHFFFAOYSA-N bis(2,3,3a,4-tetrahydro-1h-inden-1-yl)-dimethylsilane Chemical compound C1CC2CC=CC=C2C1[Si](C)(C)C1C2=CC=CCC2CC1 WPULPXOJFCAWLF-UHFFFAOYSA-N 0.000 description 1
- LFFSNSSIHWRXGF-UHFFFAOYSA-N bis(2-tert-butylcyclopenta-1,3-dien-1-yl)-dimethylsilane Chemical compound C1C=CC(C(C)(C)C)=C1[Si](C)(C)C1=C(C(C)(C)C)C=CC1 LFFSNSSIHWRXGF-UHFFFAOYSA-N 0.000 description 1
- LTOBXQFQSXFEER-UHFFFAOYSA-N bis(9h-fluoren-1-yl)-dimethylsilane Chemical compound C12=CC=CC=C2CC2=C1C=CC=C2[Si](C)(C)C1=CC=CC2=C1CC1=CC=CC=C12 LTOBXQFQSXFEER-UHFFFAOYSA-N 0.000 description 1
- YQWNAADBHGHGHH-UHFFFAOYSA-N bis(trimethylsilyl)azanide;octylaluminum(2+) Chemical compound CCCCCCCC[Al+2].C[Si](C)(C)[N-][Si](C)(C)C.C[Si](C)(C)[N-][Si](C)(C)C YQWNAADBHGHGHH-UHFFFAOYSA-N 0.000 description 1
- 238000012661 block copolymerization Methods 0.000 description 1
- 230000036760 body temperature Effects 0.000 description 1
- 238000010504 bond cleavage reaction Methods 0.000 description 1
- 229910000085 borane Inorganic materials 0.000 description 1
- 229920005605 branched copolymer Polymers 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 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
- 238000003490 calendering Methods 0.000 description 1
- KDKNVCQXFIBDBD-UHFFFAOYSA-N carbanide;1,2,3,4,5-pentamethylcyclopentane;zirconium(2+) Chemical group [CH3-].[CH3-].[Zr+2].C[C]1[C](C)[C](C)[C](C)[C]1C.C[C]1[C](C)[C](C)[C](C)[C]1C KDKNVCQXFIBDBD-UHFFFAOYSA-N 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 125000005626 carbonium group Chemical group 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000010516 chain-walking reaction Methods 0.000 description 1
- 238000003889 chemical engineering Methods 0.000 description 1
- 238000007385 chemical modification Methods 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 239000004035 construction material Substances 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 229910021419 crystalline silicon Inorganic materials 0.000 description 1
- 125000001485 cycloalkadienyl group Chemical group 0.000 description 1
- 125000000392 cycloalkenyl group Chemical group 0.000 description 1
- 125000002993 cycloalkylene group Chemical group 0.000 description 1
- ZXIJMRYMVAMXQP-UHFFFAOYSA-N cycloheptene Chemical compound C1CCC=CCC1 ZXIJMRYMVAMXQP-UHFFFAOYSA-N 0.000 description 1
- 125000003678 cyclohexadienyl group Chemical group C1(=CC=CCC1)* 0.000 description 1
- YANYHHGSVFSOTP-UHFFFAOYSA-N cyclopenta-2,4-dien-1-yl-(9H-fluoren-1-yl)-dimethylsilane Chemical compound C[Si](C1=CC=CC=2C3=CC=CC=C3CC1=2)(C1C=CC=C1)C YANYHHGSVFSOTP-UHFFFAOYSA-N 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 230000009849 deactivation Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 238000001739 density measurement Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- VQAKYCZDETUXFW-UHFFFAOYSA-N di(cyclopenta-2,4-dien-1-yl)-dimethylsilane Chemical compound C1=CC=CC1[Si](C)(C)C1C=CC=C1 VQAKYCZDETUXFW-UHFFFAOYSA-N 0.000 description 1
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 description 1
- 125000005131 dialkylammonium group Chemical group 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- RAABOESOVLLHRU-UHFFFAOYSA-N diazene Chemical compound N=N RAABOESOVLLHRU-UHFFFAOYSA-N 0.000 description 1
- 229910000071 diazene Inorganic materials 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 125000002897 diene group Chemical group 0.000 description 1
- 230000004069 differentiation Effects 0.000 description 1
- NAPSCFZYZVSQHF-UHFFFAOYSA-N dimantine Chemical compound CCCCCCCCCCCCCCCCCCN(C)C NAPSCFZYZVSQHF-UHFFFAOYSA-N 0.000 description 1
- MZFIVGBIRRZUKA-UHFFFAOYSA-N dimethyl-bis(1,2,3,4-tetramethylcyclopenta-2,4-dien-1-yl)silane Chemical compound CC1=C(C)C(C)=CC1(C)[Si](C)(C)C1(C)C(C)=C(C)C(C)=C1 MZFIVGBIRRZUKA-UHFFFAOYSA-N 0.000 description 1
- NHCUZGXLRDEZCQ-UHFFFAOYSA-N dimethyl-bis(2,3,4,9-tetrahydro-1h-fluoren-1-yl)silane Chemical compound C1C2=CC=CC=C2C(CCC2)=C1C2[Si](C)(C)C1C(CC=2C3=CC=CC=2)=C3CCC1 NHCUZGXLRDEZCQ-UHFFFAOYSA-N 0.000 description 1
- FZWVNIAFKTXYMB-UHFFFAOYSA-N dimethyl-bis(2-methyl-4-phenylinden-1-yl)silane Chemical compound CC1=CC(C(=CC=C2)C=3C=CC=CC=3)=C2[C]1[Si](C)(C)[C]1C(C)=CC2=C1C=CC=C2C1=CC=CC=C1 FZWVNIAFKTXYMB-UHFFFAOYSA-N 0.000 description 1
- GLVNPRBEFSNJTB-UHFFFAOYSA-N dimethyl-bis(2-methylinden-1-yl)silane Chemical compound C[C]1[CH][C]2C=CC=C[C]2[C]1[Si](C)(C)[C]1[C]2C=CC=C[C]2[CH][C]1C GLVNPRBEFSNJTB-UHFFFAOYSA-N 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
- UBHZUDXTHNMNLD-UHFFFAOYSA-N dimethylsilane Chemical group C[SiH2]C UBHZUDXTHNMNLD-UHFFFAOYSA-N 0.000 description 1
- AXAZMDOAUQTMOW-UHFFFAOYSA-N dimethylzinc Chemical compound C[Zn]C AXAZMDOAUQTMOW-UHFFFAOYSA-N 0.000 description 1
- HKUFIYBZNQSHQS-UHFFFAOYSA-O dioctadecylazanium Chemical compound CCCCCCCCCCCCCCCCCC[NH2+]CCCCCCCCCCCCCCCCCC HKUFIYBZNQSHQS-UHFFFAOYSA-O 0.000 description 1
- WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 description 1
- PZPGRFITIJYNEJ-UHFFFAOYSA-N disilane Chemical compound [SiH3][SiH3] PZPGRFITIJYNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 150000002019 disulfides Chemical class 0.000 description 1
- 239000012990 dithiocarbamate Substances 0.000 description 1
- 150000004659 dithiocarbamates Chemical class 0.000 description 1
- 229940069096 dodecene Drugs 0.000 description 1
- 238000011143 downstream manufacturing Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 210000004177 elastic tissue Anatomy 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000007765 extrusion coating Methods 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000013023 gasketing Methods 0.000 description 1
- 230000014509 gene expression Effects 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 150000002357 guanidines Chemical class 0.000 description 1
- 230000026030 halogenation Effects 0.000 description 1
- 238000005658 halogenation reaction Methods 0.000 description 1
- JQOAQUXIUNVRQW-UHFFFAOYSA-N hexane Chemical compound CCCCCC.CCCCCC JQOAQUXIUNVRQW-UHFFFAOYSA-N 0.000 description 1
- 229920005669 high impact polystyrene Polymers 0.000 description 1
- 229920006158 high molecular weight polymer Polymers 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 229920006258 high performance thermoplastic Polymers 0.000 description 1
- 239000004797 high-impact polystyrene Substances 0.000 description 1
- 239000007970 homogeneous dispersion Substances 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 125000000687 hydroquinonyl group Chemical class C1(O)=C(C=C(O)C=C1)* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 150000007928 imidazolide derivatives Chemical class 0.000 description 1
- QLNAVQRIWDRPHA-UHFFFAOYSA-N iminophosphane Chemical class P=N QLNAVQRIWDRPHA-UHFFFAOYSA-N 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 229910052809 inorganic oxide Inorganic materials 0.000 description 1
- 239000010954 inorganic particle Substances 0.000 description 1
- 238000006713 insertion reaction Methods 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- ICIWUVCWSCSTAQ-UHFFFAOYSA-N iodic acid Chemical class OI(=O)=O ICIWUVCWSCSTAQ-UHFFFAOYSA-N 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
- 125000000654 isopropylidene group Chemical group C(C)(C)=* 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- QANMHLXAZMSUEX-UHFFFAOYSA-N kinetin Chemical compound N=1C=NC=2N=CNC=2C=1NCC1=CC=CO1 QANMHLXAZMSUEX-UHFFFAOYSA-N 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 229920000092 linear low density polyethylene Polymers 0.000 description 1
- 239000004707 linear low-density polyethylene Substances 0.000 description 1
- 125000005647 linker group Chemical group 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 239000012968 metallocene catalyst Substances 0.000 description 1
- MPHUYCIKFIKENX-UHFFFAOYSA-N methyl 2-ethenylbenzoate Chemical compound COC(=O)C1=CC=CC=C1C=C MPHUYCIKFIKENX-UHFFFAOYSA-N 0.000 description 1
- 125000006178 methyl benzyl group Chemical group 0.000 description 1
- CAKOOJUEUVRZLR-UHFFFAOYSA-N methyl(dioctadecyl)phosphane Chemical compound CCCCCCCCCCCCCCCCCCP(C)CCCCCCCCCCCCCCCCCC CAKOOJUEUVRZLR-UHFFFAOYSA-N 0.000 description 1
- 230000001617 migratory effect Effects 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- JESXATFQYMPTNL-UHFFFAOYSA-N mono-hydroxyphenyl-ethylene Natural products OC1=CC=CC=C1C=C JESXATFQYMPTNL-UHFFFAOYSA-N 0.000 description 1
- 230000000877 morphologic effect Effects 0.000 description 1
- 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 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
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- DIOQZVSQGTUSAI-UHFFFAOYSA-N n-butylhexane Natural products CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 1
- KDFFXYVOTKKBDI-UHFFFAOYSA-N n-ethylnaphthalen-1-amine Chemical compound C1=CC=C2C(NCC)=CC=CC2=C1 KDFFXYVOTKKBDI-UHFFFAOYSA-N 0.000 description 1
- VFLWKHBYVIUAMP-UHFFFAOYSA-N n-methyl-n-octadecyloctadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCN(C)CCCCCCCCCCCCCCCCCC VFLWKHBYVIUAMP-UHFFFAOYSA-N 0.000 description 1
- SZEGKVHRCLBFKJ-UHFFFAOYSA-N n-methyloctadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCNC SZEGKVHRCLBFKJ-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 239000002071 nanotube Substances 0.000 description 1
- 239000006199 nebulizer Substances 0.000 description 1
- 125000002560 nitrile group Chemical group 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 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 1
- 238000000879 optical micrograph Methods 0.000 description 1
- 239000012766 organic filler Substances 0.000 description 1
- 239000011146 organic particle Substances 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 150000001282 organosilanes Chemical class 0.000 description 1
- 239000012285 osmium tetroxide Substances 0.000 description 1
- 229910000489 osmium tetroxide Inorganic materials 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 150000004989 p-phenylenediamines Chemical class 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- WXHIJDCHNDBCNY-UHFFFAOYSA-N palladium dihydride Chemical compound [PdH2] WXHIJDCHNDBCNY-UHFFFAOYSA-N 0.000 description 1
- 125000002097 pentamethylcyclopentadienyl group Chemical group 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical class OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
- KHIWWQKSHDUIBK-UHFFFAOYSA-N periodic acid Chemical class OI(=O)(=O)=O KHIWWQKSHDUIBK-UHFFFAOYSA-N 0.000 description 1
- 238000010060 peroxide vulcanization Methods 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- 150000004857 phospholes Chemical class 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 230000037048 polymerization activity Effects 0.000 description 1
- 238000002459 porosimetry Methods 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000012255 powdered metal Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000010734 process oil Substances 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 230000001902 propagating effect Effects 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- SHNUBALDGXWUJI-UHFFFAOYSA-N pyridin-2-ylmethanol Chemical compound OCC1=CC=CC=N1 SHNUBALDGXWUJI-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 238000004445 quantitative analysis Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 230000010076 replication Effects 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 229910052702 rhenium Inorganic materials 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 238000001175 rotational moulding Methods 0.000 description 1
- 238000010057 rubber processing Methods 0.000 description 1
- 238000010079 rubber tapping Methods 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 238000001878 scanning electron micrograph Methods 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 150000004819 silanols Chemical class 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000012306 spectroscopic technique Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 125000005346 substituted cycloalkyl group Chemical group 0.000 description 1
- 125000005648 substituted hydrocarbylene group Chemical group 0.000 description 1
- QAZLUNIWYYOJPC-UHFFFAOYSA-M sulfenamide Chemical group [Cl-].COC1=C(C)C=[N+]2C3=NC4=CC=C(OC)C=C4N3SCC2=C1C QAZLUNIWYYOJPC-UHFFFAOYSA-M 0.000 description 1
- 238000006277 sulfonation reaction Methods 0.000 description 1
- ILMRJRBKQSSXGY-UHFFFAOYSA-N tert-butyl(dimethyl)silicon Chemical group C[Si](C)C(C)(C)C ILMRJRBKQSSXGY-UHFFFAOYSA-N 0.000 description 1
- XBFJAVXCNXDMBH-UHFFFAOYSA-N tetracyclo[6.2.1.1(3,6).0(2,7)]dodec-4-ene Chemical compound C1C(C23)C=CC1C3C1CC2CC1 XBFJAVXCNXDMBH-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000007669 thermal treatment Methods 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 150000003557 thiazoles Chemical class 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- 150000003585 thioureas Chemical class 0.000 description 1
- 230000036962 time dependent Effects 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 125000005208 trialkylammonium group Chemical group 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- ZMANZCXQSJIPKH-UHFFFAOYSA-O triethylammonium ion Chemical compound CC[NH+](CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-O 0.000 description 1
- CXKQHHJKHZXXPZ-UHFFFAOYSA-N triethylsilanylium Chemical compound CC[Si+](CC)CC CXKQHHJKHZXXPZ-UHFFFAOYSA-N 0.000 description 1
- UORVGPXVDQYIDP-UHFFFAOYSA-N trihydridoboron Substances B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- VOYMPSZBODLRKS-UHFFFAOYSA-N trimethylsilanylium Chemical compound C[Si+](C)C VOYMPSZBODLRKS-UHFFFAOYSA-N 0.000 description 1
- 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 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- ZDMNAVSJDAXTBD-UHFFFAOYSA-N tris(2,3,4,5,6-pentafluorophenyl)alumane 2-undecyl-4,5-dihydro-1H-imidazole Chemical compound CCCCCCCCCCCC1=NCCN1.FC1=C(F)C(F)=C(F)C(F)=C1[Al](C=1C(=C(F)C(F)=C(F)C=1F)F)C1=C(F)C(F)=C(F)C(F)=C1F.FC1=C(F)C(F)=C(F)C(F)=C1[Al](C=1C(=C(F)C(F)=C(F)C=1F)F)C1=C(F)C(F)=C(F)C(F)=C1F ZDMNAVSJDAXTBD-UHFFFAOYSA-N 0.000 description 1
- QEPDENOFSCCDEA-UHFFFAOYSA-N tris(2,3,4,5,6-pentafluorophenyl)alumane;2-undecyl-1h-imidazole Chemical compound CCCCCCCCCCCC1=NC=CN1.FC1=C(F)C(F)=C(F)C(F)=C1[Al](C=1C(=C(F)C(F)=C(F)C=1F)F)C1=C(F)C(F)=C(F)C(F)=C1F.FC1=C(F)C(F)=C(F)C(F)=C1[Al](C=1C(=C(F)C(F)=C(F)C=1F)F)C1=C(F)C(F)=C(F)C(F)=C1F QEPDENOFSCCDEA-UHFFFAOYSA-N 0.000 description 1
- NVBHDPLKAHDQDC-UHFFFAOYSA-N tris(2,3,4,5,6-pentafluorophenyl)borane;2-undecyl-1h-imidazole Chemical compound CCCCCCCCCCCC1=NC=CN1.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.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 NVBHDPLKAHDQDC-UHFFFAOYSA-N 0.000 description 1
- MDYARPNTSPYOED-UHFFFAOYSA-N tris(2,3,4,5,6-pentafluorophenyl)borane;2-undecyl-4,5-dihydro-1h-imidazole Chemical compound CCCCCCCCCCCC1=NCCN1.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.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 MDYARPNTSPYOED-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
- OLFPYUPGPBITMH-UHFFFAOYSA-N tritylium Chemical group C1=CC=CC=C1[C+](C=1C=CC=CC=1)C1=CC=CC=C1 OLFPYUPGPBITMH-UHFFFAOYSA-N 0.000 description 1
- 239000011882 ultra-fine particle Substances 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 238000007666 vacuum forming Methods 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
- 229940117958 vinyl acetate Drugs 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 238000004260 weight control Methods 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
- 239000012991 xanthate Substances 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
- 238000010507 β-hydride elimination reaction Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
- B32B27/327—Layered products comprising a layer of synthetic resin comprising polyolefins comprising polyolefins obtained by a metallocene or single-site catalyst
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F10/14—Monomers containing five or more carbon atoms
-
- 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
- C08F210/14—Monomers containing five or more carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/16—Copolymers of ethene with alpha-alkenes, e.g. EP rubbers
-
- 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
- C08F295/00—Macromolecular compounds obtained by polymerisation using successively different catalyst types without deactivating the intermediate polymer
-
- 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
-
- 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
- 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
- C08F297/083—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 the monomers being ethylene or propylene
-
- 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
- C08F297/083—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 the monomers being ethylene or propylene
- C08F297/086—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 the monomers being ethylene or propylene the block polymer contains at least three blocks
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
- C08L23/0807—Copolymers of ethene with unsaturated hydrocarbons only containing four or more carbon atoms
- C08L23/0815—Copolymers of ethene with unsaturated hydrocarbons only containing four or more carbon atoms with aliphatic 1-olefins containing one carbon-to-carbon double bond
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/10—Homopolymers or copolymers of propene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
- C08L53/005—Modified block copolymers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F110/00—Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F110/02—Ethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2410/00—Features related to the catalyst preparation, the catalyst use or to the deactivation of the catalyst
- C08F2410/01—Additive used together with the catalyst, excluding compounds containing Al or B
-
- 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
- C08F2410/00—Features related to the catalyst preparation, the catalyst use or to the deactivation of the catalyst
- C08F2410/04—Dual catalyst, i.e. use of two different catalysts, where none of the catalysts is a metallocene
-
- 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
- C08F2420/02—Cp or analog bridged to a non-Cp X anionic donor
-
- 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
-
- 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
- C08F4/65925—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 non-bridged
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/06—Polyethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
- C08L23/0846—Copolymers of ethene with unsaturated hydrocarbons containing atoms other than carbon or hydrogen
- C08L23/0853—Ethene vinyl acetate copolymers
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24942—Structurally defined web or sheet [e.g., overall dimension, etc.] including components having same physical characteristic in differing degree
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24942—Structurally defined web or sheet [e.g., overall dimension, etc.] including components having same physical characteristic in differing degree
- Y10T428/24992—Density or compression of components
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer
- Y10T428/2813—Heat or solvent activated or sealable
- Y10T428/2817—Heat sealable
- Y10T428/2826—Synthetic resin or polymer
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
- Y10T428/31573—Next to addition polymer of ethylenically unsaturated monomer
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
- Y10T428/31573—Next to addition polymer of ethylenically unsaturated monomer
- Y10T428/31587—Hydrocarbon polymer [polyethylene, polybutadiene, etc.]
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Inorganic Chemistry (AREA)
- Graft Or Block Polymers (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Crystallography & Structural Chemistry (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US55390604P | 2004-03-17 | 2004-03-17 | |
| US60/553,906 | 2004-03-17 | ||
| PCT/US2005/008917 WO2005090427A2 (en) | 2004-03-17 | 2005-03-17 | Catalyst composition comprising shuttling agent for ethylene multi-block copolymer formation |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2559576A1 CA2559576A1 (en) | 2005-09-29 |
| CA2559576C true CA2559576C (en) | 2013-02-12 |
Family
ID=41450022
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2559576A Expired - Fee Related CA2559576C (en) | 2004-03-17 | 2005-03-17 | Catalyst composition comprising shuttling agent for ethylene multi-block copolymer formation |
Country Status (13)
| Country | Link |
|---|---|
| US (7) | US7858706B2 (enExample) |
| EP (1) | EP1727841B1 (enExample) |
| JP (1) | JP5133050B2 (enExample) |
| CN (1) | CN1976965B (enExample) |
| AT (1) | ATE461231T1 (enExample) |
| AU (1) | AU2005224259B2 (enExample) |
| BR (1) | BRPI0508148B1 (enExample) |
| CA (1) | CA2559576C (enExample) |
| DE (1) | DE602005019988D1 (enExample) |
| NO (1) | NO20064122L (enExample) |
| NZ (1) | NZ549261A (enExample) |
| WO (1) | WO2005090427A2 (enExample) |
| ZA (1) | ZA200607170B (enExample) |
Families Citing this family (520)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8357749B2 (en) | 2003-08-25 | 2013-01-22 | Dow Global Technologies Llc | Coating composition and articles made therefrom |
| US7803865B2 (en) | 2003-08-25 | 2010-09-28 | Dow Global Technologies Inc. | Aqueous dispersion, its production method, and its use |
| US9169406B2 (en) | 2003-08-25 | 2015-10-27 | Dow Global Technologies Llc | Coating compositions |
| US8779053B2 (en) | 2003-08-25 | 2014-07-15 | Dow Global Technologies Llc | Coating compositions |
| US7763676B2 (en) | 2003-08-25 | 2010-07-27 | Dow Global Technologies Inc. | Aqueous polymer dispersions and products from those dispersions |
| US8349929B2 (en) | 2003-08-25 | 2013-01-08 | Dow Global Technologies Llc | Coating composition and articles made therefrom |
| US8946329B2 (en) | 2003-08-25 | 2015-02-03 | Dow Global Technologies Llc | Coating compositions |
| US8158711B2 (en) | 2003-08-25 | 2012-04-17 | Dow Global Technologies Llc | Aqueous dispersion, its production method, and its use |
| US8722787B2 (en) | 2003-08-25 | 2014-05-13 | Dow Global Technologies Llc | Coating composition and articles made therefrom |
| US7666918B2 (en) | 2004-03-17 | 2010-02-23 | Dow Global Technologies, Inc. | Foams made from interpolymers of ethylene/α-olefins |
| US7608668B2 (en) | 2004-03-17 | 2009-10-27 | Dow Global Technologies Inc. | Ethylene/α-olefins block interpolymers |
| US7687442B2 (en) | 2004-03-17 | 2010-03-30 | Dow Global Technologies Inc. | Low molecular weight ethylene/α-olefin interpolymer as base lubricant oils |
| EP2792690B1 (en) * | 2004-03-17 | 2019-05-15 | Dow Global Technologies LLC | Catalyst composition comprising shuttling agent for ethylene multi-block copolymer formation |
| US7557147B2 (en) | 2004-03-17 | 2009-07-07 | Dow Global Technologies Inc. | Soft foams made from interpolymers of ethylene/alpha-olefins |
| US7714071B2 (en) | 2004-03-17 | 2010-05-11 | Dow Global Technologies Inc. | Polymer blends from interpolymers of ethylene/α-olefins and flexible molded articles made therefrom |
| US7795321B2 (en) | 2004-03-17 | 2010-09-14 | Dow Global Technologies Inc. | Rheology modification of interpolymers of ethylene/α-olefins and articles made therefrom |
| US8816006B2 (en) | 2004-03-17 | 2014-08-26 | Dow Global Technologies Llc | Compositions of ethylene/α-olefin multi-block interpolymer suitable for films |
| US7741397B2 (en) | 2004-03-17 | 2010-06-22 | Dow Global Technologies, Inc. | Filled polymer compositions made from interpolymers of ethylene/α-olefins and uses thereof |
| US7671131B2 (en) | 2004-03-17 | 2010-03-02 | Dow Global Technologies Inc. | Interpolymers of ethylene/α-olefins blends and profiles and gaskets made therefrom |
| JP5133050B2 (ja) | 2004-03-17 | 2013-01-30 | ダウ グローバル テクノロジーズ エルエルシー | エチレンマルチブロックコポリマーを形成するためのシャトリング剤を含む触媒組成物 |
| US7897689B2 (en) | 2004-03-17 | 2011-03-01 | Dow Global Technologies Inc. | Functionalized ethylene/α-olefin interpolymer compositions |
| US7514517B2 (en) | 2004-03-17 | 2009-04-07 | Dow Global Technologies Inc. | Anti-blocking compositions comprising interpolymers of ethylene/α-olefins |
| US7582716B2 (en) | 2004-03-17 | 2009-09-01 | Dow Global Technologies Inc. | Compositions of ethylene/α-olefin multi-block interpolymer for blown films with high hot tack |
| US7622529B2 (en) | 2004-03-17 | 2009-11-24 | Dow Global Technologies Inc. | Polymer blends from interpolymers of ethylene/alpha-olefin with improved compatibility |
| US7504347B2 (en) | 2004-03-17 | 2009-03-17 | Dow Global Technologies Inc. | Fibers made from copolymers of propylene/α-olefins |
| US8273826B2 (en) | 2006-03-15 | 2012-09-25 | Dow Global Technologies Llc | Impact modification of thermoplastics with ethylene/α-olefin interpolymers |
| US7579408B2 (en) | 2004-03-17 | 2009-08-25 | Dow Global Technologies Inc. | Thermoplastic vulcanizate comprising interpolymers of ethylene/α-olefins |
| US7524911B2 (en) | 2004-03-17 | 2009-04-28 | Dow Global Technologies Inc. | Adhesive and marking compositions made from interpolymers of ethylene/α-olefins |
| US7662881B2 (en) | 2004-03-17 | 2010-02-16 | Dow Global Technologies Inc. | Viscosity index improver for lubricant compositions |
| US7803728B2 (en) | 2004-03-17 | 2010-09-28 | Dow Global Technologies Inc. | Fibers made from copolymers of ethylene/α-olefins |
| US7622179B2 (en) | 2004-03-17 | 2009-11-24 | Dow Global Technologies Inc. | Three dimensional random looped structures made from interpolymers of ethylene/α-olefins and uses thereof |
| US8273838B2 (en) | 2004-03-17 | 2012-09-25 | Dow Global Technologies Llc | Propylene/α-olefins block interpolymers |
| US7355089B2 (en) | 2004-03-17 | 2008-04-08 | Dow Global Technologies Inc. | Compositions of ethylene/α-olefin multi-block interpolymer for elastic films and laminates |
| AU2005322952B2 (en) | 2005-01-03 | 2012-04-26 | Dow Global Technologies Llc | Elastomeric resin compositions with improved resistance to draw resonance |
| MY158058A (en) * | 2005-03-17 | 2016-08-30 | Dow Global Technologies Inc | ADHESIVE AND MARKING COMPOSITIONS MADE FROM INTERPOLYMERS OF ETHYLENE/a-OLEFINS |
| US7737215B2 (en) | 2005-03-17 | 2010-06-15 | Dow Global Technologies Inc. | Compositions of ethylene/α-olefin multi-block interpolymer for elastic films and laminates |
| BRPI0609815B1 (pt) * | 2005-03-17 | 2018-11-06 | Dow Global Technologies Inc | composição polimérica |
| KR101319124B1 (ko) * | 2005-03-17 | 2013-10-23 | 다우 글로벌 테크놀로지스 엘엘씨 | 상용성이 개선된 에틸렌/알파-올레핀의 혼성중합체로부터의중합체 블렌드 |
| CN101553512B (zh) * | 2005-03-17 | 2011-11-23 | 陶氏环球技术有限责任公司 | 包括乙烯/α-烯烃共聚体的防粘连组合物 |
| JP5227162B2 (ja) * | 2005-03-17 | 2013-07-03 | ダウ グローバル テクノロジーズ エルエルシー | エチレン/α−オレフィンの共重合体由来のポリマーブレンドおよびそれから製造される可撓性成形品 |
| RU2007134378A (ru) * | 2005-03-17 | 2009-03-20 | Дау Глобал Текнолоджиз Инк. (Us) | ТРЕХМЕРНЫЕ СТАТИСТИЧЕСКИЕ ПЕРЕПЛЕТЕННЫЕ СТРУКТУРЫ, ИЗГОТОВЛЕННЫЕ ИЗ ИНТЕРПОЛИМЕРОВ ЭТИЛЕНА/α-ОЛЕФИНОВ, И ИХ ПРИМЕНЕНИЕ |
| TWI374150B (en) * | 2005-03-17 | 2012-10-11 | Dow Global Technologies Llc | Filled polymer compositions made from interpolymers of ethylene α-olefins and uses thereof |
| BR122017015865B1 (pt) * | 2005-03-17 | 2019-10-01 | Dow Global Technologies Inc. | Mistura polimérica, perfil, gaxeta, espuma e artigo termoformado |
| BRPI0609837A2 (pt) * | 2005-03-17 | 2010-05-04 | Dow Global Technologies Inc | composição lubrificante |
| JP5570115B2 (ja) * | 2005-03-17 | 2014-08-13 | ダウ グローバル テクノロジーズ エルエルシー | 擬似ブロックコポリマーおよび可逆的連鎖移動剤(chainshuttlingagent)を用いる方法 |
| ES2673179T3 (es) * | 2005-03-17 | 2018-06-20 | Dow Global Technologies Llc | Composiciones de interpolímero multibloque de etileno/alfa-olefina para películas sopladas con alta pegajosidad en caliente |
| CA2600318A1 (en) * | 2005-03-17 | 2006-09-28 | Dow Global Technologies Inc. | Catalyst composition comprising shuttling agent for regio-irregular multi-block copolymer formation |
| US9410009B2 (en) * | 2005-03-17 | 2016-08-09 | Dow Global Technologies Llc | Catalyst composition comprising shuttling agent for tactic/ atactic multi-block copolymer formation |
| BRPI0609814B1 (pt) * | 2005-03-17 | 2019-01-15 | Dow Global Technologies Inc | espuma, composição espumável e artigo espumado |
| TW200641115A (en) * | 2005-03-17 | 2006-12-01 | Dow Global Technologies Inc | Low molecular weight ethylene/ α-olefin interpolymer as base lubricant oils |
| KR101399699B1 (ko) * | 2005-03-17 | 2014-05-27 | 다우 글로벌 테크놀로지스 엘엘씨 | 관능화된 에틸렌/α-올레핀 혼성중합체 조성물 |
| EP1869095B1 (en) * | 2005-03-17 | 2011-04-27 | Dow Global Technologies LLC | Compositions of ethylene/alpha-olefin multi-block interpolymer for elastic films and laminates |
| JP5227163B2 (ja) * | 2005-03-17 | 2013-07-03 | ダウ グローバル テクノロジーズ エルエルシー | エチレン/α−オレフィン共重合体での熱可塑性物質の耐衝撃性改良 |
| CA2601292A1 (en) * | 2005-03-17 | 2006-09-28 | Dow Global Technologies Inc. | Ethylene/alpha-olefins block interpolymers |
| CA2601245A1 (en) * | 2005-03-17 | 2006-09-28 | Dow Global Technologies Inc. | Interpolymers of ethylene/alpha-olefins blends and profiles and gaskets made therefrom |
| US8981028B2 (en) * | 2005-03-17 | 2015-03-17 | Dow Global Technologies Llc | Catalyst composition comprising shuttling agent for tactic/ atactic multi-block copolymer formation |
| US7910658B2 (en) | 2005-03-17 | 2011-03-22 | Dow Global Technologies Llc | Compositions of ethylene/α-olefin multi-block interpolymer for elastic films and laminates |
| US7786216B2 (en) * | 2005-03-17 | 2010-08-31 | Dow Global Technologies Inc. | Oil based blends of interpolymers of ethylene/α-olefins |
| CA2601376A1 (en) * | 2005-03-17 | 2006-09-28 | Dow Global Technologies Inc. | Fibers made from copolymers of ethylene/alpha-olefins |
| BRPI0609828A2 (pt) * | 2005-03-17 | 2010-04-27 | Dow Global Technologies Inc | pelìcula e composição apropriada para pelìculas |
| RU2404299C2 (ru) * | 2005-03-17 | 2010-11-20 | Дау Глобал Текнолоджиз Инк. | ВОЛОКНА, ИЗГОТОВЛЕННЫЕ ИЗ СОПОЛИМЕРОВ ПРОПИЛЕНА/α-ОЛЕФИНОВ |
| MY142099A (en) * | 2005-03-17 | 2010-09-15 | Dow Global Technologies Inc | Cap liners, closures and gaskets from multi-block polymers |
| JP5305898B2 (ja) * | 2005-03-17 | 2013-10-02 | ダウ グローバル テクノロジーズ エルエルシー | エチレン/α−オレフィンの共重合体を含む熱可塑性加硫物 |
| US8287949B2 (en) * | 2005-07-07 | 2012-10-16 | Dow Global Technologies Inc. | Aqueous dispersions |
| US7947787B2 (en) * | 2005-09-15 | 2011-05-24 | Dow Global Technologies Llc | Control of polymer architecture and molecular weight distribution via multi-centered shuttling agent |
| AR058450A1 (es) * | 2005-09-15 | 2008-02-06 | Dow Global Technologies Inc | Copolimeros de bloque de olefina cataliticos con distibucion de secuencia de bloque controlada |
| TW200722441A (en) * | 2005-09-15 | 2007-06-16 | Dow Global Technologies Inc | Catalytic olefin block copolymers via polymerizable shuttling agent |
| US7906587B2 (en) * | 2005-09-16 | 2011-03-15 | Dow Global Technologies Llc | Polymer blends from interpolymer of ethylene/α olefin with improved compatibility |
| EP3428329B1 (en) * | 2005-10-26 | 2020-11-25 | Dow Global Technologies LLC | A fiber comprising a low crystallinity polymer and a high crystallinity polymer |
| US8153243B2 (en) | 2005-12-09 | 2012-04-10 | Dow Global Technologies Llc | Interpolymers suitable for multilayer films |
| CN103788276B (zh) * | 2005-12-09 | 2017-10-17 | 陶氏环球技术有限责任公司 | 乙烯/α‑烯烃组合物中控制分子量分布的方法 |
| US7528080B2 (en) | 2005-12-15 | 2009-05-05 | Dow Global Technologies, Inc. | Aqueous polyolefin dispersions for textile impregnation |
| US8029646B2 (en) | 2005-12-15 | 2011-10-04 | Dow Global Technologies Llc | Cellulose articles containing an additive composition |
| WO2008156454A1 (en) | 2007-06-21 | 2008-12-24 | Kimberly-Clark Worldwide, Inc. | Wiping products having enhanced oil absorbency |
| US7879191B2 (en) | 2005-12-15 | 2011-02-01 | Kimberly-Clark Worldwide, Inc. | Wiping products having enhanced cleaning abilities |
| US8043713B2 (en) | 2005-12-15 | 2011-10-25 | Dow Global Technologies Llc | Compositions and aqueous dispersions |
| WO2007071438A1 (en) | 2005-12-23 | 2007-06-28 | Dsm Ip Assets B.V. | Use of thermoplastic elastomers in floor covering for animal housing |
| JP2009526925A (ja) | 2006-02-15 | 2009-07-23 | ダウ グローバル テクノロジーズ インコーポレイティド | 架橋ポリエチレン弾性繊維 |
| US8074295B2 (en) | 2006-05-03 | 2011-12-13 | Dow Global Technologies Llc | Stretchable fabric suitable for swimwear applications |
| US8785531B2 (en) | 2006-07-06 | 2014-07-22 | Dow Global Technologies Llc | Dispersions of olefin block copolymers |
| CN101511578A (zh) | 2006-07-14 | 2009-08-19 | 陶氏环球技术公司 | 各向异性泡沫-薄膜复合结构 |
| US20080115825A1 (en) | 2006-09-20 | 2008-05-22 | Patel Rajen M | Electronic Device Module Comprising an Ethylene Multi-Block Copolymer |
| CN101517750B (zh) | 2006-09-20 | 2011-06-29 | 陶氏环球技术有限责任公司 | 包括乙烯多嵌段共聚物的电子器件模块 |
| US8476326B2 (en) | 2006-09-22 | 2013-07-02 | Dow Global Technologies Llc | Fibrillated polyolefin foam |
| US8207265B2 (en) | 2006-10-30 | 2012-06-26 | Dow Global Technologies Llc | Adhesives films |
| EP2084222B1 (en) | 2006-11-01 | 2010-03-17 | Dow Global Technologies Inc. | Polyurethane compositions and articles prepared therefrom, and methods for making the same |
| US7928022B2 (en) | 2006-11-30 | 2011-04-19 | Dow Global Technologies Llc | Olefin block compositions for heavy weight stretch fabrics |
| US7785443B2 (en) | 2006-12-07 | 2010-08-31 | Kimberly-Clark Worldwide, Inc. | Process for producing tissue products |
| US7741407B2 (en) | 2006-12-13 | 2010-06-22 | Acushnet Company | Catalyst compositions comprising chain shuttling agents and the use thereof to produce golf ball compositions |
| KR101458236B1 (ko) | 2006-12-21 | 2014-11-04 | 다우 글로벌 테크놀로지스 엘엘씨 | 관능화된 올레핀 중합체, 조성물 및 그로부터 제조된 물품, 및 그의 제조 방법 |
| WO2008124127A1 (en) * | 2007-04-09 | 2008-10-16 | The Regents Of The University Of California | Soft and strong elastomeric compositions from semicrystalline-amorphous polyolefin block copolymers |
| WO2008134186A1 (en) | 2007-04-24 | 2008-11-06 | Dow Global Technologies Inc. | THERMOFORMING, SCRATCH-RESISTANT, LOW GLOSS COMPOSITIONS COMPRISING INTERPOLYMERS OF ETHYLENE/α-OLEFINS |
| ITMI20070877A1 (it) | 2007-05-02 | 2008-11-03 | Dow Global Technologies Inc | Processo per la produzione di copolimeri a blocchi multipli con l'utilizzo di solventi polari |
| ITMI20070878A1 (it) | 2007-05-02 | 2008-11-03 | Dow Global Technologies Inc | Processo per la polimerizzazine di polimeri tattici con l'uso di catalizzatori chirali |
| BRPI0810327A2 (pt) * | 2007-05-04 | 2014-10-14 | Dow Global Technologies Inc | Mistura não compatibilizada, pocesso para reparar uma mistura não compatibilizada e processo melhorado de moldagem por sopro com estiramento |
| US8569422B2 (en) | 2007-07-13 | 2013-10-29 | Dow Global Technologies, Llc | Catalytic olefin block copolymers with controlled block sequence distribution and at least one low crystallinity hard block |
| US8492322B2 (en) | 2007-07-13 | 2013-07-23 | Dow Global Technologies, Llc | Viscosity index improver for lubricant compositions |
| EP2170604B1 (en) | 2007-07-13 | 2019-05-15 | Dow Global Technologies LLC | Ethylene/alpha-olefin interpolymers having low crystallinity hard blocks |
| CN101802150A (zh) * | 2007-07-13 | 2010-08-11 | 陶氏环球技术公司 | 润滑剂组合物的粘度指数改性剂 |
| WO2010008371A1 (en) * | 2008-06-30 | 2010-01-21 | Dow Global Technologies Inc. | Polyolefin compositions and articles prepared therefrom and methods of making the same |
| DE502008002049D1 (de) | 2007-08-13 | 2011-02-03 | Tesa Se | Trennmittel auf Basis von Ethylen-multi-Blockcopolymer |
| EP2025506B1 (de) | 2007-08-13 | 2010-11-03 | Tesa Se | Klebeband mit einem Träger aus zumindest einer Schaumschicht |
| TR201808249T4 (tr) * | 2007-09-24 | 2018-07-23 | Dow Global Technologies Llc | Şok absorpsiyon tabanlı sentetik çim. |
| WO2009045731A2 (en) | 2007-09-28 | 2009-04-09 | Dow Global Technologies Inc. | Dispersions of higher crystallinity olefins |
| WO2009043946A1 (es) | 2007-10-02 | 2009-04-09 | Dow Global Technologies Inc. | Métodos para la reducción de aditivos polares necesarios para uso en poliolefinas |
| EP2052857A1 (en) | 2007-10-22 | 2009-04-29 | Dow Global Technologies Inc. | Multilayer films |
| JP5357169B2 (ja) | 2007-10-22 | 2013-12-04 | ダウ グローバル テクノロジーズ エルエルシー | 物品を成形するためのポリマー組成物及び方法 |
| WO2009064993A1 (en) | 2007-11-15 | 2009-05-22 | Dow Global Technologies Inc. | A coating composition, a coated article, and method of forming such articles |
| WO2009064942A1 (en) | 2007-11-15 | 2009-05-22 | Dow Global Technologies Inc. | A coating composition, a coated article, and method of forming such articles |
| WO2009067337A1 (en) | 2007-11-19 | 2009-05-28 | Dow Global Technologies Inc. | Long chain branched propylene-alpha-olefin copolymers |
| EP3779034A3 (en) | 2007-12-21 | 2021-02-24 | Dow Global Technologies Llc | Method for making a carpet using olefin block copolymers |
| EP2080615A1 (en) | 2008-01-18 | 2009-07-22 | Dow Global Technologies Inc. | Coated substrates and packages prepared therefrom |
| JP5697997B2 (ja) * | 2008-02-29 | 2015-04-08 | ダウ グローバル テクノロジーズ エルエルシー | エチレン/α−オレフィンインターポリマーから作製される繊維及び布地 |
| WO2009105938A1 (en) | 2008-02-29 | 2009-09-03 | Dow Global Technologies Inc. | Oriented films comprising ethylene/α-olefin block interpolymer |
| US8404773B2 (en) | 2008-03-17 | 2013-03-26 | Dow Global Technologies Llc | Coating composition, method of producing the same, articles made therefrom, and method of making such articles |
| JP5327684B2 (ja) | 2008-06-03 | 2013-10-30 | ダウ グローバル テクノロジーズ エルエルシー | 複合分散液、その製造方法、及びそれから製造された物品 |
| WO2009155155A1 (en) | 2008-06-18 | 2009-12-23 | Dow Global Technologies Inc. | Processes to control fouling and improve compositions |
| DK3243939T3 (da) | 2008-08-18 | 2020-05-18 | Transhield Inc | Polyethylen-fibre med høj varmebestandighedstempera-tur og ikke-vævede stoffer omfattende dem |
| BRPI0912921A2 (pt) | 2008-08-21 | 2017-05-23 | Dow Global Technologies Llc | complexo metal-ligante, catalisador e processo para preparo de uma poliolefina |
| US8772414B2 (en) | 2008-09-16 | 2014-07-08 | Dow Global Technologies Llc | Polymeric compositions and foams, methods of making the same, and articles prepared from the same |
| CN102239213A (zh) | 2008-10-03 | 2011-11-09 | 陶氏环球技术有限责任公司 | 具有乙烯/α-烯烃互聚物的聚合物共混物 |
| KR101621575B1 (ko) | 2008-10-10 | 2016-05-16 | 다우 글로벌 테크놀로지스 엘엘씨 | 종이계 기재용 다층 코팅 |
| KR101490546B1 (ko) | 2008-10-17 | 2015-02-05 | 다우 글로벌 테크놀로지스 엘엘씨 | 필름 구조물 및 그 필름 구조물을 갖는 판지 |
| CN102202885B (zh) | 2008-11-06 | 2013-11-13 | 陶氏环球技术有限责任公司 | 电子器件组件用的共挤出的、多层的基于聚烯烃的背板 |
| JP2010126557A (ja) * | 2008-11-25 | 2010-06-10 | Mitsui Chemicals Inc | オレフィンブロック重合体の製造方法 |
| US20100129663A1 (en) * | 2008-11-26 | 2010-05-27 | 3M Innovative Properties Company | Surfacing film for composite structures |
| JP5548699B2 (ja) | 2008-12-22 | 2014-07-16 | ダウ グローバル テクノロジーズ エルエルシー | 織りカーペット用塗料化合物、関連使用方法、及びそれらから造られる物品 |
| US9021611B2 (en) | 2009-02-18 | 2015-04-28 | Northwestern University | Beam pen lithography |
| EP2757113A2 (en) | 2009-03-06 | 2014-07-23 | Dow Global Technologies LLC | Catalysts, processes for making catalysts, processes for making polyolefin compositions and polyolefin compositions |
| CN102414258B (zh) | 2009-03-16 | 2014-03-26 | 陶氏环球技术有限责任公司 | 分散体、和制备该分散体的方法 |
| EP2995449A1 (en) | 2009-03-20 | 2016-03-16 | Dow Global Technologies LLC | Multilayer structure and method of making the same |
| US8105463B2 (en) | 2009-03-20 | 2012-01-31 | Kimberly-Clark Worldwide, Inc. | Creped tissue sheets treated with an additive composition according to a pattern |
| KR20120000571A (ko) | 2009-03-30 | 2012-01-02 | 다우 글로벌 테크놀로지스 엘엘씨 | 하이브리드 분산액 및 그의 제조 방법 |
| ES2935812T3 (es) | 2009-04-10 | 2023-03-10 | Dow Global Technologies Llc | Película de polipropileno orientada biaxialmente de alto rendimiento coextrudida y sellable |
| JP2012524683A (ja) * | 2009-04-23 | 2012-10-18 | 東レバッテリーセパレータフィルム株式会社 | 熱可塑性フィルム、かかるフィルムの製造方法、およびバッテリーセパレーターフィルムとしてのかかるフィルムの使用 |
| CN102459357B (zh) | 2009-06-05 | 2013-07-31 | 陶氏环球技术有限责任公司 | 制备乙烯的长链支化的(lcb)嵌段共聚物或互连共聚物的方法 |
| US8722817B2 (en) * | 2009-06-05 | 2014-05-13 | Dow Global Technologies Llc | Process to make long chain branched (LCB), block, or interconnected copolymers of ethylene |
| KR20120023736A (ko) * | 2009-06-05 | 2012-03-13 | 미쓰이 가가쿠 가부시키가이샤 | 태양전지 봉지막의 보존용 또는 운반용 포장체, 및 태양전지 봉지막의 보존 또는 운반 방법 |
| US9243087B2 (en) | 2009-06-11 | 2016-01-26 | Dow Global Technologies Llc | LDPE enabling high output and good optics when blended with other polymers |
| US8318874B2 (en) | 2009-06-26 | 2012-11-27 | Dow Global Technologies Llc | Process of selectively polymerizing ethylene and catalyst therefor |
| CN102481770B (zh) | 2009-07-01 | 2016-12-21 | 陶氏环球技术有限责任公司 | 乙烯类聚合物及其用途 |
| US9885149B2 (en) | 2009-07-08 | 2018-02-06 | Dow Global Technologies Llc | Carpet and carpet backing |
| SG177650A1 (en) | 2009-07-15 | 2012-03-29 | Dow Global Technologies Llc | Polymer compositions, methods of making the same, and articles prepared from the same |
| CN102217091B (zh) | 2009-07-17 | 2012-11-21 | 三菱树脂株式会社 | 太阳能电池封装材料以及使用该封装材料制作的太阳能电池组件 |
| CN104691907B (zh) | 2009-07-24 | 2017-09-08 | 陶氏环球技术有限责任公司 | 涂布的容器装置或涂布的闭合装置 |
| EP2456680B1 (en) | 2009-07-24 | 2017-05-31 | Dow Global Technologies LLC | A coated container device, method of making the same |
| EP3243846B1 (en) | 2009-07-29 | 2021-01-06 | Dow Global Technologies LLC | Multi-headed chain shuttling agents and their use for the preparation of block copolymers |
| BR112012001942B1 (pt) | 2009-07-29 | 2019-10-22 | Dow Global Technologies Llc | agente de permuta de cadeia multifuncional, processo para preparar um agente de permuta de cadeia multifuncional, processo para preparar uma composição multifuncional, composição multifuncional, processo para preparar um agente de permuta de cadeia multifuncional contendo poli-radical poliolefina, poliolefina telequélica, processo para preparar uma poliolefina com funcionalidade terminal e separador de bateria |
| WO2011016992A2 (en) | 2009-07-29 | 2011-02-10 | Dow Global Technologies Inc. | Polymeric chain transfer/shuttling agents |
| WO2011019563A1 (en) | 2009-08-10 | 2011-02-17 | Dow Global Technologies Inc. | Ldpe for use as a blend component in shrinkage film applications |
| EP2473538B1 (en) * | 2009-08-31 | 2017-07-26 | Dow Global Technologies LLC | Catalyst and process for polymerizing an olefin and polyolefin prepared thereby |
| JP2013504205A (ja) | 2009-09-01 | 2013-02-04 | ダウ グローバル テクノロジーズ エルエルシー | リジッドな光起電力モジュール用のバックシート |
| EP2478025B1 (en) | 2009-09-14 | 2018-12-05 | Dow Global Technologies LLC | Polymers comprising units derived from ethylene and siloxane |
| CN102597029B (zh) | 2009-09-14 | 2014-09-17 | 陶氏环球技术有限责任公司 | 包含源自乙烯和聚(烷氧基化物)的单元的聚合物 |
| CN102695734B (zh) | 2009-09-14 | 2015-05-06 | 陶氏环球技术有限责任公司 | 包含源于乙烯和聚链烯的单元的聚合物 |
| CN102725345B (zh) | 2009-09-18 | 2014-12-10 | 陶氏环球技术有限责任公司 | 用于凝塑成形工艺的粉末热塑性聚烯烃弹性体组合物 |
| BR112012007272B1 (pt) | 2009-10-02 | 2021-08-10 | Dow Global Technologies Llc | Composição formulada, composição modificada para impacto e artigo |
| CN102770487B (zh) | 2009-10-02 | 2014-10-01 | 陶氏环球技术有限责任公司 | 热塑性硫化材料应用中的嵌段复合材料 |
| JP2013506743A (ja) | 2009-10-02 | 2013-02-28 | ダウ グローバル テクノロジーズ エルエルシー | ソフトコンパウンドにおけるブロックコポリマー |
| US8476366B2 (en) | 2009-10-02 | 2013-07-02 | Dow Global Technologies, Llc | Block compositions in thermoplastic vulcanizate applications |
| BR112012011927A2 (pt) | 2009-11-20 | 2020-09-24 | Dow Global Technologies Llc | primeira composição de elastômero termoplástico, segunda composição e artigo |
| US9278473B2 (en) | 2009-12-04 | 2016-03-08 | Union Carbide Chemicals & Plastics Technology Llc | Extruder screw |
| CN102652140A (zh) | 2009-12-15 | 2012-08-29 | 住友化学株式会社 | 烯烃聚合催化剂和烯烃聚合物的生产方法 |
| WO2011072459A1 (en) | 2009-12-18 | 2011-06-23 | Dow Global Technologies Llc. | Halogen-free, flame retardant compositions for wire and cable applications |
| EP2513226B1 (en) | 2009-12-18 | 2017-05-03 | Dow Global Technologies LLC | Halogen-free, flame retardant compositions |
| CN102762653B (zh) | 2009-12-31 | 2015-11-25 | 陶氏环球技术有限责任公司 | 用于电线和电缆应用的无卤素阻燃热塑性组合物 |
| JP5837514B2 (ja) | 2010-02-19 | 2015-12-24 | ダウ グローバル テクノロジーズ エルエルシー | 金属−配位子錯体及び触媒 |
| SG183310A1 (en) | 2010-02-19 | 2012-09-27 | Dow Global Technologies Llc | Process for polymerizing an olefin monomer and catalyst therefor |
| KR101668146B1 (ko) | 2010-02-22 | 2016-10-20 | 다우 글로벌 테크놀로지스 엘엘씨 | 도장된 폴리올레핀 물품 |
| EP2374917B1 (en) | 2010-04-07 | 2013-02-13 | Dow Global Technologies LLC | Artificial turf yarn |
| JP2011225670A (ja) * | 2010-04-16 | 2011-11-10 | Tosoh Corp | 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 |
| JP2011225669A (ja) * | 2010-04-16 | 2011-11-10 | Tosoh Corp | 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 |
| KR20130106277A (ko) | 2010-05-10 | 2013-09-27 | 다우 글로벌 테크놀로지스 엘엘씨 | 접착 촉진제 시스템, 및 그의 제조 방법 |
| CN107033808B (zh) | 2010-05-10 | 2020-01-17 | 陶氏环球技术有限责任公司 | 助粘剂及其制备方法 |
| MX350592B (es) | 2010-05-17 | 2017-09-11 | Dow Global Tech Llc * | Proceso para polimerizacion selectiva de etileno y un catalizador del mismo. |
| WO2011144039A1 (en) | 2010-05-21 | 2011-11-24 | Dow Global Technologies Llc | Thermoplastic compositions and formed articles thereof |
| CN102971371B (zh) | 2010-05-27 | 2016-02-10 | 陶氏环球技术有限责任公司 | 聚合物组合物、其制备方法和由其制备的制品 |
| EP2576688B1 (en) | 2010-05-27 | 2017-01-18 | Dow Global Technologies LLC | Polymer compositions, methods of making the same, and articles prepared from the same |
| WO2011149886A1 (en) | 2010-05-28 | 2011-12-01 | Dow Global Technologies Llc | Heat-sealable polyolefin-based film comprising olefin block copolymer |
| CN102933651B (zh) | 2010-06-08 | 2016-05-04 | 陶氏环球技术有限责任公司 | 用于人造革应用的聚烯烃弹性体组合物 |
| WO2011156742A2 (en) * | 2010-06-10 | 2011-12-15 | University Of Maryland, College Park | Living coordinative chain transfer polymerization with dynamic counterion exchange |
| EP2580286B1 (en) | 2010-06-14 | 2015-05-06 | Dow Global Technologies LLC | Olefin block copolymer composition with low tack |
| CN103079817B (zh) | 2010-06-17 | 2015-11-25 | 陶氏环球技术有限责任公司 | 单面拉伸粘附膜 |
| KR101818792B1 (ko) | 2010-06-18 | 2018-01-15 | 유니온 카바이드 케미칼즈 앤드 플라스틱스 테크날러지 엘엘씨 | 전기 전도성 올레핀 멀티블록 공중합체 조성물 |
| US9607728B2 (en) | 2010-06-18 | 2017-03-28 | Dow Global Technologies Llc | Electrically conductive, mesophase-separated olefin multiblock copolymer compositions |
| JP2013530284A (ja) | 2010-06-18 | 2013-07-25 | ダウ グローバル テクノロジーズ エルエルシー | 被覆されたポリマー微粒子、及びポリマー微粒子を被覆するための方法 |
| SG186414A1 (en) | 2010-06-21 | 2013-01-30 | Dow Global Technologies Llc | Crystalline block composites as compatibilizers |
| CN103097453B (zh) | 2010-06-21 | 2015-08-05 | 陶氏环球技术有限责任公司 | 用作增容剂的结晶嵌段复合材料 |
| JP5860043B2 (ja) * | 2010-06-21 | 2016-02-16 | ダウ グローバル テクノロジーズ エルエルシー | 相溶化剤としての結晶性ブロック複合体 |
| US8822599B2 (en) | 2010-06-21 | 2014-09-02 | Dow Global Technologies Llc | Crystalline block composites as compatibilizers |
| BR112012028633B1 (pt) | 2010-06-22 | 2020-10-13 | Dow Global Technologies Inc | composição reticulada e artigo |
| IT1400743B1 (it) | 2010-06-30 | 2013-07-02 | Dow Global Technologies Inc | Composizioni polimeriche |
| US8445393B2 (en) | 2010-07-27 | 2013-05-21 | Kimberly-Clark Worldwide, Inc. | Low-density web and method of applying an additive composition thereto |
| WO2012015624A1 (en) | 2010-07-27 | 2012-02-02 | Dow Global Technologies Llc | Low-density web and method of applying an additive composition thereto |
| JP5625060B2 (ja) | 2010-07-28 | 2014-11-12 | 三菱樹脂株式会社 | 太陽電池封止材及びそれを用いて作製された太陽電池モジュール |
| ES2659733T3 (es) | 2010-08-25 | 2018-03-19 | Dow Global Technologies Llc | Proceso de polimerización de olefina polimerizable y catalizador para ello |
| JP5968321B2 (ja) | 2010-09-30 | 2016-08-10 | ダウ グローバル テクノロジーズ エルエルシー | ポリマー組成物およびそれを用いたシーラント層 |
| US8907034B2 (en) | 2010-09-30 | 2014-12-09 | Dow Global Technologies Llc | Comb architecture olefin block copolymers |
| MX340414B (es) | 2010-09-30 | 2016-07-06 | Dow Global Tech Llc * | Composición polimérica y capa selladora con la misma. |
| WO2012061706A1 (en) | 2010-11-04 | 2012-05-10 | Dow Global Technologies Llc | Double shuttling of polyolefin polymeryl chains |
| CN103229312B (zh) | 2010-11-30 | 2016-09-21 | 大日本印刷株式会社 | 太阳能电池用多层体及使用其制作的太阳能电池模块 |
| CN103562301B (zh) | 2010-12-30 | 2017-10-20 | 陶氏环球技术有限责任公司 | 组合物、其制备方法和由其制备的制品 |
| JP5859567B2 (ja) | 2010-12-30 | 2016-02-10 | ダウ グローバル テクノロジーズ エルエルシー | マイクロクリスタリンワックスを含む抗ブリード性油展オレフィンブロックコポリマー組成物 |
| KR101858290B1 (ko) | 2010-12-30 | 2018-05-15 | 다우 글로벌 테크놀로지스 엘엘씨 | 침전 실리카를 포함한, 오일-증량 내용출성 올레핀 블록 공중합체 조성물 |
| CN103314042B (zh) | 2011-01-03 | 2017-08-08 | 陶氏环球技术有限责任公司 | 包含功能填料材料的微毛细管膜和泡沫体 |
| ES2637156T3 (es) | 2011-01-03 | 2017-10-11 | Dow Global Technologies Llc | Películas y espumas reforzadas con microcapilares |
| EP2663400A4 (en) | 2011-01-14 | 2014-07-30 | Grace W R & Co | PROCESS FOR THE PREPARATION OF A MODIFIED METALLOCENE CATALYST, CATALYST THUS PRODUCED AND USE THEREOF |
| WO2012103080A1 (en) | 2011-01-26 | 2012-08-02 | Dow Global Technologies Llc | Process for making a polyolefin-polysiloxane block copolymer |
| SG192089A1 (en) | 2011-01-27 | 2013-08-30 | Lg Chemical Ltd | Olefin block copolymer |
| US8835563B2 (en) | 2011-03-25 | 2014-09-16 | Exxonmobil Chemical Patents Inc. | Block copolymers from silylated vinyl terminated macromers |
| US8399724B2 (en) | 2011-03-25 | 2013-03-19 | Exxonmobil Chemical Patents Inc. | Vinyl terminated higher olefin copolymers and methods to produce thereof |
| US8623974B2 (en) | 2011-03-25 | 2014-01-07 | Exxonmobil Chemical Patents Inc. | Branched vinyl terminated polymers and methods for production thereof |
| US8940839B2 (en) | 2011-03-25 | 2015-01-27 | Exxonmobil Chemical Patents Inc. | Diblock copolymers prepared by cross metathesis |
| US8841397B2 (en) | 2011-03-25 | 2014-09-23 | Exxonmobil Chemical Patents Inc. | Vinyl terminated higher olefin polymers and methods to produce thereof |
| BR112013034072B1 (pt) | 2011-04-08 | 2021-02-17 | Rohm And Haas Company | composição de revestimento, uma ou mais camadas de revestimento e artigo |
| WO2012153786A1 (ja) * | 2011-05-09 | 2012-11-15 | 独立行政法人理化学研究所 | 多元重合体の製造方法、および多元重合体 |
| US9296836B2 (en) | 2011-05-12 | 2016-03-29 | Dow Global Technologies Llc | Non-cyclopentadienyl-based chromium catalysts for olefin polymerization |
| KR101248423B1 (ko) | 2011-06-09 | 2013-04-02 | 에스케이종합화학 주식회사 | 에틸렌 - α-올레핀 - 디엔 공중합체의 제조방법 |
| WO2012174422A2 (en) | 2011-06-17 | 2012-12-20 | Berry Plastics Corporation | Insulated container with molded brim |
| CN105600061B (zh) | 2011-06-17 | 2018-03-20 | 比瑞塑料公司 | 绝热容器 |
| ES2592530T3 (es) | 2011-06-17 | 2016-11-30 | Fiberweb, Llc | Artículo de múltiples capas permeable al vapor, sustancialmente impermeable al agua |
| CN103717113B (zh) | 2011-06-17 | 2015-11-25 | 比瑞塑料公司 | 用于杯子的绝热套筒 |
| WO2012174567A2 (en) | 2011-06-17 | 2012-12-20 | Berry Plastics Corporation | Process for forming an insulated container having artwork |
| CN103748639B (zh) | 2011-06-21 | 2017-03-01 | 陶氏环球技术有限责任公司 | 含有基于哌嗪的泡沸阻燃剂的无卤素阻燃聚合物组合物 |
| DK2723568T3 (en) | 2011-06-23 | 2017-10-23 | Fiberweb Llc | Vapor permeable, essentially all water impermeable, multilayer |
| US10369769B2 (en) | 2011-06-23 | 2019-08-06 | Fiberweb, Inc. | Vapor-permeable, substantially water-impermeable multilayer article |
| WO2012178011A2 (en) | 2011-06-24 | 2012-12-27 | Fiberweb, Inc. | Vapor-permeable, substantially water-impermeable multilayer article |
| KR101967493B1 (ko) | 2011-06-30 | 2019-04-09 | 다우 글로벌 테크놀로지스 엘엘씨 | 결정질 블록 공중합체 복합체 또는 블록 공중합체 복합체를 포함하는 층을 포함하는 통합된 배면시트 및 봉지 성능을 갖는 다층 폴리올레핀-기재의 필름 |
| CN103764396B (zh) | 2011-06-30 | 2016-05-18 | 陶氏环球技术有限责任公司 | 具有包含结晶嵌段共聚物复合材料或嵌段共聚物复合材料树脂的层的多层基于聚烯烃的膜 |
| JP5852239B2 (ja) | 2011-07-20 | 2016-02-03 | ダウ コーニング コーポレーションDow Corning Corporation | 亜鉛含有錯体及び縮合反応触媒、この触媒を調製する方法、及びこの触媒を含有する組成物 |
| JP5757566B2 (ja) * | 2011-07-26 | 2015-07-29 | リケンテクノス株式会社 | 発泡成形用熱可塑性エラストマー組成物 |
| WO2013016398A1 (en) | 2011-07-28 | 2013-01-31 | Dow Global Technologies Llc | Polymeric blend formulations suitable for synthetic leather applications |
| ES2486615B2 (es) | 2011-08-31 | 2017-03-08 | Berry Plastics Corporation | Formulación, resina o extruido para conformar una estructura celular aislante, polimérica y no aromática, artículo y material que se obtiene, recipiente conformado y proceso de obtención. |
| JP6066355B2 (ja) | 2011-09-07 | 2017-01-25 | ダウ コーニング コーポレーションDow Corning Corporation | ジルコニウム含有錯体及び縮合反応触媒、該触媒の調製方法、及び該触媒を含有する組成物 |
| CN103781823B (zh) | 2011-09-07 | 2016-08-17 | 道康宁公司 | 含钛络合物和缩合反应催化剂、制备该催化剂的方法以及包含该催化剂的组合物 |
| WO2014021908A1 (en) | 2011-09-20 | 2014-02-06 | Dow Corning Corporation | Iridium containing hydrosilylation catalysts and compositions containing the catalysts |
| JP6101695B2 (ja) | 2011-09-20 | 2017-03-22 | ダウ コーニング コーポレーションDow Corning Corporation | ニッケル含有ヒドロシリル化触媒及びその触媒を含有する組成物 |
| CN103814038A (zh) | 2011-09-20 | 2014-05-21 | 道康宁公司 | 含钌硅氢加成催化剂及含有该催化剂的组合物 |
| CN103842441B (zh) | 2011-10-04 | 2015-12-23 | 道康宁公司 | 含铁(iii)络合物和缩合反应催化剂、制备该催化剂的方法及含有该催化剂的组合物 |
| US9139699B2 (en) | 2012-10-04 | 2015-09-22 | Dow Corning Corporation | Metal containing condensation reaction catalysts, methods for preparing the catalysts, and compositions containing the catalysts |
| WO2013081794A1 (en) | 2011-12-01 | 2013-06-06 | Dow Corning Corporation | Hydrosilylation reaction catalysts and curable compositions and methods for their preparation and use |
| CN103958548B (zh) * | 2011-12-02 | 2016-05-18 | 住友化学株式会社 | 使用多种过渡金属催化剂的烯烃嵌段聚合物的制造方法 |
| IN2014CN04286A (enExample) | 2011-12-14 | 2015-09-04 | Dow Global Technologies Llc | |
| CN104245834B (zh) | 2011-12-14 | 2017-10-13 | 陶氏环球技术有限责任公司 | 官能化的嵌段复合材料和结晶嵌段复合材料组合物 |
| US8501882B2 (en) | 2011-12-19 | 2013-08-06 | Chevron Phillips Chemical Company Lp | Use of hydrogen and an organozinc compound for polymerization and polymer property control |
| WO2013096696A1 (en) | 2011-12-20 | 2013-06-27 | Dow Global Technologies Llc | A rotomolding composition |
| CN104245290B (zh) | 2011-12-22 | 2020-05-08 | 陶氏环球技术有限责任公司 | 适合于毛细管作用流体输送的微毛细管膜和泡沫体 |
| US9464177B2 (en) | 2011-12-30 | 2016-10-11 | Dow Global Technologies Llc | Foam composition with olefin block copolymer gel particles |
| US20140377576A1 (en) | 2011-12-30 | 2014-12-25 | Dow Global Technologies Llc | Adhesion Promoter Composition for Polyolefin Substrate |
| CN104040730B (zh) | 2012-01-13 | 2017-03-08 | 大日本印刷株式会社 | 外观良好的太阳能电池组件及其制造方法 |
| JP6318619B2 (ja) | 2012-02-06 | 2018-05-09 | 大日本印刷株式会社 | 太陽電池用封止シート |
| WO2013134083A1 (en) | 2012-03-07 | 2013-09-12 | Dow Global Technologies Llc | Polyolefin based formulations for membranes and fabrics |
| US20150025165A1 (en) * | 2012-03-16 | 2015-01-22 | Dow Global Technologies Llc | Foamable compositions, foams and articles thereof |
| EP2831190B1 (en) | 2012-03-30 | 2016-12-14 | Dow Global Technologies LLC | Polyolefin adhesive composition |
| WO2013147186A1 (ja) | 2012-03-30 | 2013-10-03 | 三菱レイヨン株式会社 | 複合中空糸膜及び中空糸膜モジュール |
| US20130281340A1 (en) | 2012-04-19 | 2013-10-24 | Exxonmobil Chemical Patents Inc. | Lubricant Compositions Comprising Ethylene Propylene Copolymers and Methods for Making Them |
| US8952105B2 (en) | 2012-05-23 | 2015-02-10 | Baker Hughes Incorporated | Variable TG article, method of making, and use of same |
| WO2013183344A1 (ja) | 2012-06-07 | 2013-12-12 | 三菱樹脂株式会社 | 太陽電池モジュール及びその製造方法 |
| BR112014029687B1 (pt) | 2012-06-19 | 2021-01-19 | Dow Global Technologies Llc | composição de mistura base água, processo para produzir uma composição de mistura base água, película, película de multicamadas e dispositivo recipiente |
| EP2861664B1 (en) | 2012-06-19 | 2016-11-16 | Dow Global Technologies LLC | Aqueous based blend composition and method of producing the same |
| EP2864543B1 (en) | 2012-06-22 | 2017-10-11 | Trinseo Europe GmbH | A coated substrate and system and method for making the same |
| US9607732B2 (en) | 2012-06-27 | 2017-03-28 | Dow Global Technologies Llc | Polymeric coatings for coated conductors |
| PL2866999T3 (pl) | 2012-06-28 | 2020-03-31 | Dow Global Technologies Llc | Sposób wytwarzania wielowarstwowej folii mikrokapilarnej |
| JP6122111B2 (ja) | 2012-06-28 | 2017-04-26 | ダウ グローバル テクノロジーズ エルエルシー | 多層マイクロキャピラリーフィルムの製造システム、方法、および装置 |
| KR102032886B1 (ko) | 2012-06-29 | 2019-10-21 | 다우 글로벌 테크놀로지스 엘엘씨 | 열가소성 가황물용 에틸렌/알파-올레핀/비공액 폴리엔 기재 조성물 |
| WO2014004287A1 (en) | 2012-06-29 | 2014-01-03 | Dow Global Technologies Llc | Stain resistant article with olefin block copolymer and process |
| US9713906B2 (en) | 2012-08-07 | 2017-07-25 | Berry Plastics Corporation | Cup-forming process and machine |
| WO2014035483A1 (en) | 2012-08-28 | 2014-03-06 | Dow Brasil S.A. | Films containing functional ethylene-based polymer compostions |
| WO2014035467A1 (en) | 2012-08-29 | 2014-03-06 | Dow Global Technologies Llc | Ethylene-based polymer compositions and foams |
| KR102173723B1 (ko) | 2012-08-31 | 2020-11-03 | 다우 글로벌 테크놀로지스 엘엘씨 | 필름에 적합한 내열성 폴리올레핀 조성물 |
| EP2890300B1 (en) | 2012-08-31 | 2019-01-02 | Kenji Suzuki | Supervised machine learning technique for reduction of radiation dose in computed tomography imaging |
| EP2899077B1 (en) | 2012-09-19 | 2016-12-21 | Mitsubishi Chemical Corporation | Airbag housing cover |
| WO2014066761A1 (en) | 2012-10-26 | 2014-05-01 | Berry Plastics Corporation | Polymeric material for an insulated container |
| EP2732963A1 (en) | 2012-11-15 | 2014-05-21 | Dow Global Technologies LLC | Extrusion coated textile laminate with improved peel strength |
| AR093944A1 (es) | 2012-12-14 | 2015-07-01 | Berry Plastics Corp | Troquelado para envase |
| AR093943A1 (es) | 2012-12-14 | 2015-07-01 | Berry Plastics Corp | Reborde de un envase termico |
| US9840049B2 (en) | 2012-12-14 | 2017-12-12 | Berry Plastics Corporation | Cellular polymeric material |
| PL2931518T3 (pl) | 2012-12-17 | 2019-08-30 | Dow Global Technologies Llc | Struktura wielowarstwowa i sposób uszczelniania lub kształtowania przy użyciu struktury wielowarstwowej |
| CN104903070B (zh) | 2012-12-27 | 2018-05-01 | 陶氏环球技术有限责任公司 | 通过反向旋转挤压制造热塑性聚烯烃屋顶膜 |
| SG11201505122VA (en) | 2012-12-28 | 2015-07-30 | Dow Global Technologies Llc | Bleed resistant, oil-extended olefin block copolymer composition with surface-active agent |
| EP2938490B1 (en) | 2012-12-28 | 2020-04-15 | Dow Global Technologies LLC | Multilayer films containing functional ethylene-based polymer compositions |
| US20140187114A1 (en) | 2012-12-28 | 2014-07-03 | Dow Brasil S.A. | Elastic nonwovens with improved haptics and mechanical properties |
| BR112015015408B1 (pt) | 2012-12-28 | 2021-07-20 | Dow Global Technologies Llc | Composição de revestimento, e, artigo revestido |
| CN105026502B (zh) | 2012-12-28 | 2020-12-04 | 陶氏环球技术有限责任公司 | 涂料组合物和由其制成的物品 |
| BR112015014048B1 (pt) | 2012-12-31 | 2021-09-08 | Dow Global Technologies Llc | Composição e composição de termoplástico vulcanizado |
| CN104884561B (zh) | 2012-12-31 | 2017-05-03 | 陶氏环球技术有限责任公司 | 具有硅烷接枝的烯烃嵌段共聚物的压敏粘着剂组合物 |
| WO2014111292A1 (en) | 2013-01-18 | 2014-07-24 | Basf Se | Acrylic dispersion-based coating compositions |
| US8680218B1 (en) * | 2013-01-30 | 2014-03-25 | Chevron Phillips Chemical Company Lp | Methods for controlling dual catalyst olefin polymerizations with an organozinc compound |
| US9034477B2 (en) | 2013-03-05 | 2015-05-19 | Dow Global Technologies Llc | Coating composition, a film containing the same, and a method for forming a sealable film |
| CN105008416B (zh) | 2013-03-06 | 2017-08-01 | 埃克森美孚化学专利公司 | 利用吡啶基二氨基催化剂的聚烯烃聚合中可逆的链转移 |
| US9957365B2 (en) | 2013-03-13 | 2018-05-01 | Berry Plastics Corporation | Cellular polymeric material |
| US20140262916A1 (en) | 2013-03-14 | 2014-09-18 | Berry Plastics Corporation | Container |
| KR102235294B1 (ko) | 2013-04-18 | 2021-04-02 | 롬 앤드 하스 캄파니 | 올레핀 블록 공중합체를 함유하는 압출가능한 접착제 배합물 |
| JP2014234404A (ja) * | 2013-05-31 | 2014-12-15 | 東ソー株式会社 | ポリオレフィン系被覆電線 |
| US10040888B1 (en) | 2013-06-14 | 2018-08-07 | Cooper-Standard Automotive Inc. | Composition including silane-grafted polyolefin |
| CN108047381B (zh) | 2013-07-01 | 2021-02-02 | 罗门哈斯公司 | 复合聚合物组合物 |
| WO2015002859A2 (en) | 2013-07-02 | 2015-01-08 | Dow Global Technologies Llc | Polyolefin/ (meth)acrylic impact modifier and method of preparing same |
| US10100139B2 (en) | 2013-08-01 | 2018-10-16 | Cooper-Standard Automotive Inc. | Hose, composition including silane-grafted polyolefin, and process of making a hose |
| WO2015021201A1 (en) | 2013-08-08 | 2015-02-12 | Dow Global Technologies Llc | A composite material, articles made therefrom |
| WO2015024018A1 (en) | 2013-08-16 | 2015-02-19 | Berry Plastics Corporation | Polymeric material for an insulated container |
| RU2671854C2 (ru) | 2013-08-20 | 2018-11-07 | Ром Энд Хаас Компани | Связующие композиции, содержащие олефиновые блочные сополимеры, для фиксирующих устройств |
| US9931781B2 (en) | 2013-08-26 | 2018-04-03 | Berry Plastics Corporation | Polymeric material for container |
| MX375055B (es) | 2013-09-20 | 2025-03-06 | Dow Global Technologies Llc | Proceso para desgasificar cables de transporte de energia reticulados. |
| KR102519282B1 (ko) | 2013-10-15 | 2023-04-10 | 다우 글로벌 테크놀로지스 엘엘씨 | 혼화성 폴리올레핀 블렌드 |
| CA2927060C (en) | 2013-10-18 | 2021-03-30 | Dow Global Technologies Llc | Optical fiber cable components |
| CA2927156C (en) | 2013-10-18 | 2021-10-26 | Dow Global Technologies Llc | Optical fiber cable components |
| WO2015061440A1 (en) | 2013-10-25 | 2015-04-30 | Dow Global Technologies Llc | Polyethylene and polypropylene composition suitable for the use as retortable easy opening seals |
| BR112016009343B1 (pt) | 2013-11-08 | 2022-01-04 | Dow Global Technologies Llc | Composição de tinta sem iniciador, artigo e método |
| CA2933637C (en) | 2013-12-18 | 2021-10-26 | Dow Global Technologies Llc | Optical fiber cable components |
| BR112016014773A2 (pt) * | 2013-12-23 | 2017-08-08 | Braskem America Inc | Composição, artigo de fabricação, e, método para fazer uma composição |
| KR102267196B1 (ko) | 2013-12-31 | 2021-06-22 | 다우 글로벌 테크놀로지스 엘엘씨 | 에틸렌/α-올레핀 다중-블록 공중합체를 갖는 핫 멜트 접착제 조성물 |
| EP2921519A1 (en) | 2014-03-17 | 2015-09-23 | Dow Global Technologies LLC | A multilayer structure |
| US9714306B2 (en) | 2014-03-28 | 2017-07-25 | Mitsui Chemicals, Inc. | Olefin resin and method for producing same |
| ES2866158T3 (es) | 2014-04-09 | 2021-10-19 | Dow Global Technologies Llc | Películas de polietileno orientado y un método para fabricar las mismas |
| US20170226321A1 (en) | 2014-06-24 | 2017-08-10 | Dow Global Technologies Llc | Polyolefin Photovoltaic Backsheet Comprising a Stabilized Polypropylene Layer |
| JP2017525142A (ja) | 2014-06-24 | 2017-08-31 | ダウ グローバル テクノロジーズ エルエルシー | 有機粘土を含む光起電力モジュール |
| US11760851B2 (en) | 2014-06-30 | 2023-09-19 | Formosa Plastics Corporation, U.S.A. | Cast film component layer exhibiting an outstanding cling property |
| US10371292B2 (en) | 2014-07-02 | 2019-08-06 | Cooper-Standard Automotive Inc. | Hose, abrasion resistant composition, and process of making a hose |
| WO2016004618A1 (en) | 2014-07-11 | 2016-01-14 | Dow Global Technologies Llc | Composition and article of manufacture comprising thereof |
| US10421258B2 (en) | 2014-08-13 | 2019-09-24 | Performance Materials Na, Inc. | Multilayer structure comprising polypropylene |
| US10026522B1 (en) * | 2014-08-19 | 2018-07-17 | Superior Essex International LP | Flame retardant insulation material for use in a plenum cable |
| SG11201701351TA (en) | 2014-08-21 | 2017-03-30 | Dow Global Technologies Llc | Hot melt adhesive composition including a crystalline block composite |
| KR102242739B1 (ko) | 2014-08-21 | 2021-04-22 | 다우 글로벌 테크놀로지스 엘엘씨 | 결정성 블록 복합체를 포함하는 핫멜트 접착제 |
| US9758655B2 (en) | 2014-09-18 | 2017-09-12 | Berry Plastics Corporation | Cellular polymeric material |
| EP3197675B1 (en) | 2014-09-25 | 2022-11-23 | Dow Global Technologies LLC | Polyolefin-based elastic film structures, laminates and methods thereof |
| BR112017005065A2 (pt) | 2014-09-26 | 2018-01-23 | Dow Global Technologies Llc | uma estrutura de multicamadas |
| CN107075227B (zh) | 2014-10-02 | 2020-07-10 | 陶氏环球技术有限责任公司 | 具有良好阻燃性的高频可焊乙烯类聚合物组合物 |
| CA2965306C (en) | 2014-10-29 | 2023-02-28 | Dow Global Technologies Llc | Olefin block composite thermally conductive materials |
| WO2016093266A1 (ja) | 2014-12-09 | 2016-06-16 | 三井化学株式会社 | プロピレン系樹脂組成物 |
| US10513589B2 (en) | 2015-01-23 | 2019-12-24 | Berry Plastics Corporation | Polymeric material for an insulated container |
| MX2017009858A (es) | 2015-01-30 | 2017-11-15 | Braskem America Inc | Polipropileno modificado y mezclas de polimero del mismo. |
| WO2016141179A1 (en) | 2015-03-04 | 2016-09-09 | Berry Plastics Corporation | Polymeric material for container |
| TWI688524B (zh) * | 2015-03-17 | 2020-03-21 | 美商陶氏全球科技有限責任公司 | 用於撓性容器之撓性配件 |
| TWI703041B (zh) | 2015-03-17 | 2020-09-01 | 美商陶氏全球科技有限責任公司 | 用於將撓性配件密封至撓性膜之方法 |
| ES2863574T3 (es) | 2015-03-18 | 2021-10-11 | Dow Global Technologies Llc | Películas protectoras, mezclas y métodos de fabricación de las mismas |
| WO2016148897A1 (en) | 2015-03-18 | 2016-09-22 | Dow Global Technologies Llc | Method to make an elastormeric polyolefin skin |
| US10723892B2 (en) | 2015-03-31 | 2020-07-28 | Dow Global Technologies Llc | Spray dried polyolefin elastomer powder for rotational molding processes |
| JP6779230B2 (ja) | 2015-05-11 | 2020-11-04 | ダウ グローバル テクノロジーズ エルエルシー | 改質剤を有する高メルトフロー熱可塑性ポリオレフィン |
| AR104645A1 (es) | 2015-05-29 | 2017-08-02 | Dow Global Technologies Llc | Composición adhesiva para película de múltiples capas que puede volver a cerrarse |
| EP3313950A4 (en) * | 2015-06-29 | 2018-11-21 | Dow Global Technologies LLC | Article with adhesive composition having a block composite compatibilizer |
| US20180291169A1 (en) | 2015-06-30 | 2018-10-11 | Dow Global Technologies Llc | Blends for foams, foams manufactured therefrom and articles comprising the same |
| WO2017003762A1 (en) | 2015-06-30 | 2017-01-05 | Dow Global Technologies Llc | Polypropylene/inorganic particle blend composition for pvc-free wear layer in resilient flooring |
| EP3317340B1 (en) | 2015-06-30 | 2019-04-17 | Dow Global Technologies LLC | Polymeric forulation with dirt pick-up resistance |
| AR105372A1 (es) | 2015-07-27 | 2017-09-27 | Dow Global Technologies Llc | Laminados elásticos, métodos para su fabricación y artículos que los comprenden |
| AR105371A1 (es) | 2015-07-27 | 2017-09-27 | Dow Global Technologies Llc | Composiciones elásticas basadas en poliolefina, métodos para su fabricación y artículos que los comprenden |
| WO2017044533A1 (en) | 2015-09-10 | 2017-03-16 | Dow Global Technologies Llc | Polyolefin blends including polyoctene with compatibilizer |
| WO2017044547A1 (en) | 2015-09-10 | 2017-03-16 | Dow Global Technologies Llc | Polyolefin blends including compatibilizer |
| KR102606493B1 (ko) | 2015-09-17 | 2023-11-28 | 다우 글로벌 테크놀로지스 엘엘씨 | 감소된 발화 민감도를 가진 폴리머 코팅물 조성물 |
| US9701456B2 (en) | 2015-09-30 | 2017-07-11 | Dow Global Technologies Llc | Flexible container with extendable spout |
| US10071837B2 (en) | 2015-09-30 | 2018-09-11 | Dow Global Technologies Llc | Fitment with valve and ethylene/a-olefin multi-block copolymer |
| BR112018004696B1 (pt) | 2015-09-30 | 2022-06-28 | Dow Global Technologies Llc | Processo para a preparação de um polímero funcional |
| TW201713575A (zh) | 2015-09-30 | 2017-04-16 | 陶氏全球科技有限責任公司 | 具有乙烯/α-烯烴多嵌段共聚物的配件 |
| JP6832348B2 (ja) | 2015-09-30 | 2021-02-24 | ダウ グローバル テクノロジーズ エルエルシー | 連鎖シャトリングに有用な多頭性または二頭性組成物、及びそれを調製するためのプロセス |
| US10414887B2 (en) | 2015-10-02 | 2019-09-17 | Exxonmobil Chemical Patents Inc. | Supported catalyst systems and methods of using same |
| US10668670B2 (en) | 2015-10-30 | 2020-06-02 | Dow Global Technologies Llc | Process for sealing flexible fitment to flexible film |
| TW201733560A (zh) | 2015-10-30 | 2017-10-01 | 陶氏全球科技有限責任公司 | 具有隔膜及乙烯/α-烯烴多嵌段共聚物之端口 |
| BR112018010314B1 (pt) | 2015-12-10 | 2022-01-25 | Dow Global Technologies Llc | Composição, processo de fabricação de um tubo, tubo e cabo |
| US11608590B2 (en) | 2016-02-19 | 2023-03-21 | Teknor Apex Company | Fiber forming compositions, fibers and methods for production |
| EP3430066B1 (en) | 2016-03-14 | 2023-02-22 | Dow Global Technologies LLC | Process for preparing foamed articles made from ethylene/alpha-olefin interpolymers |
| CA3018594C (en) | 2016-03-25 | 2023-06-27 | Dow Global Technologies Llc | Buffer tubes for fiber optic cables |
| BR112018069915B1 (pt) | 2016-03-31 | 2022-08-16 | Dow Global Technologies Llc | Composição e artigo |
| WO2017176997A1 (en) | 2016-04-08 | 2017-10-12 | Avery Dennison Corporation | Clear hot melt adhesives |
| AR108467A1 (es) | 2016-05-27 | 2018-08-22 | Dow Global Technologies Llc | Accesorio con componente de mezcla y contenedor flexible con el mismo |
| BR112018074402B1 (pt) | 2016-05-31 | 2022-10-18 | Dow Global Technologies Llc | Composição e artigo |
| CN109844010B (zh) | 2016-05-31 | 2021-12-07 | 陶氏环球技术有限责任公司 | 具有改善的低温冲击性能的热塑性聚烯烃共混物 |
| WO2017214099A1 (en) | 2016-06-08 | 2017-12-14 | Dow Global Technologies Llc | Method to make a composite automotive trim part |
| RU2753758C2 (ru) | 2016-06-23 | 2021-08-23 | Дау Глоубл Текнолоджиз Ллк | Материал для многокомпонентного формования на поликарбонате |
| TW201809046A (zh) | 2016-07-29 | 2018-03-16 | 陶氏全球科技有限責任公司 | 半結晶熱塑性嵌段共聚物 |
| US20190169411A1 (en) | 2016-08-12 | 2019-06-06 | Dow Global Technologies Llc | Propylene-based compositions comprising carbon fibers and a thermoplastic polyolefin elastomer |
| EP3293002A1 (en) | 2016-09-09 | 2018-03-14 | Dow Global Technologies LLC | Multilayer films and laminates and packages formed from same |
| TW201829598A (zh) | 2016-09-12 | 2018-08-16 | 美商陶氏全球科技有限責任公司 | 用於低溫用容器之抗衝擊改質組合物 |
| WO2018057078A1 (en) | 2016-09-21 | 2018-03-29 | Exxonmobil Chemical Patents Inc. | Compositions of olefin block copolymers and propylene-based elastomers |
| US10227483B2 (en) | 2016-09-21 | 2019-03-12 | Exxonmobil Chemical Patents Inc. | Compositions of olefin block copolymers and propylene-based elastomers |
| US10858505B2 (en) | 2016-09-22 | 2020-12-08 | Dow Global Technologies Llc | Polyethylene compositions, and articles made therefrom |
| CN109715724B (zh) | 2016-09-22 | 2022-07-22 | 陶氏环球技术有限责任公司 | 聚乙烯组合物和由其制成的制品 |
| US10155615B2 (en) | 2016-09-26 | 2018-12-18 | Dow Global Technologies Llc | Seal bar and process for using same |
| US10173821B2 (en) | 2016-09-26 | 2019-01-08 | Dow Global Technologies Llc | Flexible fitment for flexible container |
| US20180086526A1 (en) | 2016-09-28 | 2018-03-29 | Dow Global Technologies Llc | Flexible Container with Tube Member |
| CN109996920B (zh) | 2016-09-28 | 2022-06-17 | 陶氏环球技术有限责任公司 | 经涂布的聚酯织物 |
| BR112019005873B1 (pt) | 2016-09-28 | 2022-10-04 | Dow Global Technologies Llc | Bolsa de retorta |
| US11098188B2 (en) | 2016-09-29 | 2021-08-24 | Dow Global Technologies Llc | Blends for foams, foams manufactured therefrom and articles comprising the same |
| EP3519520B1 (en) | 2016-09-29 | 2022-05-18 | Dow Global Technologies Llc | Polymer compositions for uv curable primers |
| US10173813B2 (en) | 2016-09-29 | 2019-01-08 | Dow Global Technologies Llc | Flexible container with pop-up spout |
| CN109937217B (zh) | 2016-09-30 | 2021-09-14 | 陶氏环球技术有限责任公司 | 适用于链梭移的多头或双头组合物和其制备方法 |
| JP7029448B2 (ja) | 2016-09-30 | 2022-03-03 | ダウ グローバル テクノロジーズ エルエルシー | チェーンシャトリングに有用な封鎖されたマルチまたはデュアルヘッド組成物、およびそれを調製するプロセス |
| CN109963888A (zh) | 2016-09-30 | 2019-07-02 | 陶氏环球技术有限责任公司 | 用于制备适用于链梭移的多头或双头组合物的方法 |
| CN109803824A (zh) | 2016-10-12 | 2019-05-24 | 陶氏环球技术有限责任公司 | 多层结构、包含多层结构的物品,及制作多层结构的方法 |
| US11370860B2 (en) | 2016-10-19 | 2022-06-28 | Exxonmobil Chemical Patents Inc. | Supported catalyst systems and methods of using same |
| JP6792646B2 (ja) | 2016-12-10 | 2020-11-25 | クーパー−スタンダード・オートモーティブ・インコーポレーテッド | マイクロ高密度シール、組成物、およびこれらを作製する方法 |
| CN110352129B (zh) | 2016-12-10 | 2021-09-03 | 库珀标准汽车公司 | 屋面膜、制造其的组合物和方法 |
| SG11201907497PA (en) | 2017-02-20 | 2019-09-27 | Exxonmobil Chemical Patents Inc | Supported catalyst systems and processes for use thereof |
| US10723819B2 (en) | 2017-02-20 | 2020-07-28 | Exxonmobil Chemical Patents, Inc. | Supported catalyst systems and processes for use thereof |
| EP3372401B1 (en) | 2017-03-10 | 2020-02-05 | Dow Global Technologies Llc | Multilayer films and methods thereof |
| KR102648625B1 (ko) * | 2017-03-15 | 2024-03-19 | 다우 글로벌 테크놀로지스 엘엘씨 | 다중-블록 공중합체 형성을 위한 촉매 시스템 |
| CN115260366B (zh) * | 2017-03-15 | 2025-01-28 | 陶氏环球技术有限责任公司 | 用于形成多嵌段共聚物的催化剂体系 |
| BR112019019076A2 (pt) | 2017-03-15 | 2020-06-30 | Dow Global Technologies Llc | sistema catalisador de formação de copolímeros de múltiplos blocos |
| JP7179750B2 (ja) * | 2017-03-15 | 2022-11-29 | ダウ グローバル テクノロジーズ エルエルシー | マルチブロックコポリマー形成用触媒系 |
| US11208502B2 (en) | 2017-03-15 | 2021-12-28 | Dow Global Technologies Llc | Catalyst system for multi-block coploymer formation |
| US11028192B2 (en) | 2017-03-27 | 2021-06-08 | Exxonmobil Chemical Patents Inc. | Solution process to make ethylene copolymers |
| TW201843044A (zh) | 2017-04-28 | 2018-12-16 | 美商陶氏全球科技有限責任公司 | 具有黏著劑層之物品 |
| BR112019024784A2 (pt) | 2017-05-31 | 2020-06-09 | Dow Global Technologies Llc | método para revestimento de uma junta de montagem de tubulação |
| CN110662796A (zh) | 2017-06-06 | 2020-01-07 | 陶氏环球技术有限责任公司 | 制造汽车装饰复合部件的方法 |
| EP3645623B1 (en) | 2017-06-29 | 2021-05-19 | Dow Global Technologies LLC | Plastic living hinges with block composite polymer |
| US11312119B2 (en) | 2017-07-18 | 2022-04-26 | Dow Global Technologies Llc | Resins, multilayer films and packages comprising the same |
| EP3431546A1 (en) | 2017-07-18 | 2019-01-23 | Dow Global Technologies Llc | Resins, multilayer films and packages comprising the same |
| US10844150B2 (en) | 2017-08-04 | 2020-11-24 | Exxonmobil Chemical Patents Inc. | Mixed catalysts with 2,6-bis(imino)pyridyl iron complexes and bridged hafnocenes |
| SG11202000942TA (en) | 2017-08-04 | 2020-02-27 | Exxonmobil Chemical Patents Inc | Mixed catalysts with unbridged hafnocenes with -ch2-sime3 moieties |
| CA3013585A1 (en) | 2017-08-08 | 2019-02-08 | Berry Global, Inc. | Insulated container |
| WO2019041216A1 (en) | 2017-08-31 | 2019-03-07 | Dow Global Technologies Llc | PROCESS FOR PRODUCING FOAM BALLS USING A MODIFIED ETHYLENE POLYMER |
| EP3681717B1 (en) | 2017-09-05 | 2024-01-24 | Dow Global Technologies LLC | Multilayer film with reversible haze |
| EP3687787B1 (en) | 2017-09-27 | 2021-07-28 | Dow Global Technologies LLC | Abrasion resistant flexible composites and multilayer pipe liners for cured-in-place pipe |
| TW201917141A (zh) | 2017-10-25 | 2019-05-01 | 美商陶氏全球科技有限責任公司 | 雙組份纖維之三維毛圈材料 |
| US10703838B2 (en) | 2017-10-31 | 2020-07-07 | Exxonmobil Chemical Patents Inc. | Mixed catalyst systems with four metallocenes on a single support |
| CN109777081A (zh) * | 2017-11-10 | 2019-05-21 | 丹阳市日晟工业设备有限公司 | 一种绝缘塑料件 |
| US10926250B2 (en) | 2017-12-01 | 2021-02-23 | Exxonmobil Chemical Patents Inc. | Catalyst systems and polymerization processes for using the same |
| WO2019108977A1 (en) | 2017-12-01 | 2019-06-06 | Exxonmobil Chemical Patents Inc. | Catalyst systems and polymerization processes for using the same |
| EA202091173A1 (ru) | 2017-12-18 | 2020-11-12 | Бореалис Аг | Композиция из смеси полимеров для применения в области проводов и кабелей с преимущественными электрическими свойствами |
| WO2019125050A1 (ko) * | 2017-12-22 | 2019-06-27 | 주식회사 엘지화학 | 올레핀계 중합체 |
| US11542352B2 (en) * | 2017-12-26 | 2023-01-03 | Lg Chem, Ltd. | Olefin-based polymer |
| KR102574823B1 (ko) | 2017-12-28 | 2023-09-06 | 다우 글로벌 테크놀로지스 엘엘씨 | 올레핀 다중 블록 공중합체 / 실리콘 고무 조성물 및 이들로부터 형성된 폼 |
| WO2019127186A1 (en) | 2017-12-28 | 2019-07-04 | Dow Global Technologies Llc | Olefin multi-block copolymer/silicone rubber/tackifier compositions and foams |
| CN119684341A (zh) | 2017-12-29 | 2025-03-25 | 陶氏环球技术有限责任公司 | 双头有机铝组合物 |
| JP7381464B2 (ja) | 2017-12-29 | 2023-11-15 | ダウ グローバル テクノロジーズ エルエルシー | 末端保護された双頭型有機アルミニウム組成物 |
| US10865258B2 (en) | 2018-01-31 | 2020-12-15 | Exxonmobil Chemical Patents Inc. | Mixed catalyst systems containing bridged metallocenes with a pendant group 13 element, processes for making a polymer product using same, and products made from same |
| US10851187B2 (en) | 2018-01-31 | 2020-12-01 | Exxonmobil Chemical Patents Inc. | Bridged metallocene catalysts with a pendant group 13 element, catalyst systems containing same, processes for making a polymer product using same, and products made from same |
| KR20200133354A (ko) | 2018-03-19 | 2020-11-27 | 다우 글로벌 테크놀로지스 엘엘씨 | 규소-말단화된 오르가노-금속 화합물 및 이의 제조방법 |
| BR112020019174A2 (pt) | 2018-03-19 | 2021-01-05 | Dow Global Technologies Llc | Composições de poliolefina telequélica terminadas com silício e processos para a preparação das mesmas |
| JP2021518460A (ja) | 2018-03-19 | 2021-08-02 | ダウ シリコーンズ コーポレーション | ポリオレフィン−ポリジオルガノシロキサンコポリマーを含有するホットメルト接着剤組成物ならびにその調製方法および使用方法 |
| WO2019182992A1 (en) | 2018-03-19 | 2019-09-26 | Dow Global Technologies Llc | Process for functionalization of organo-zinc compounds with halosilanes using basic nitrogen containing heterocycles and silyl-functionalized compounds prepared thereby |
| TW201938570A (zh) | 2018-03-19 | 2019-10-01 | 美商陶氏全球科技有限責任公司 | 矽封端之有機金屬化合物及其製備方法 |
| CN112074547A (zh) | 2018-03-19 | 2020-12-11 | 陶氏环球技术有限责任公司 | 用基于硅烷基的官能化试剂官能化有机金属化合物的方法和由此制备的硅烷基官能化化合物 |
| WO2019182721A1 (en) | 2018-03-19 | 2019-09-26 | Dow Silicones Corporation | Polyolefin-polydiorganosiloxane block copolymer and hydrosilylaton reaction method for the synthesis thereof |
| JP7263381B2 (ja) | 2018-03-19 | 2023-04-24 | ダウ シリコーンズ コーポレーション | ポリオレフィン-ポリジオルガノオシロキサン(polydiorganoosiloxane)コポリマーを含有するポリオルガノシロキサンホットメルト接着剤組成物ならびにそれを調製および使用するための方法 |
| US12037462B2 (en) | 2018-03-19 | 2024-07-16 | Dow Global Technologies Llc | Polyolefin-polydiorganosiloxane block copolymer and method for the synthesis thereof |
| CN112041351B (zh) | 2018-03-30 | 2023-12-29 | 陶氏环球技术有限责任公司 | 高度可溶的双硼酸盐作为烯烃聚合的双核助催化剂 |
| JP7499181B2 (ja) | 2018-03-30 | 2024-06-13 | ダウ グローバル テクノロジーズ エルエルシー | オレフィン重合活性化剤 |
| KR20200138272A (ko) | 2018-03-30 | 2020-12-09 | 다우 글로벌 테크놀로지스 엘엘씨 | 올레핀 중합 활성화제 |
| SG11202008667SA (en) | 2018-03-30 | 2020-10-29 | Dow Global Technologies Llc | Binuclear olefin polymerization activators |
| SG11202008655RA (en) | 2018-03-30 | 2020-10-29 | Dow Global Technologies Llc | Highly soluble alkyl substituted carbenium borate as co-catalysts for olefin polymerizations |
| JP6944602B2 (ja) | 2018-04-17 | 2021-10-06 | ヘンケル アイピー アンド ホールディング ゲゼルシャフト ミット ベシュレンクテル ハフツング | 接触接着剤およびその使用 |
| JP7408571B2 (ja) | 2018-05-03 | 2024-01-05 | ダウ グローバル テクノロジーズ エルエルシー | 優れた柔軟性と熱風溶接性を備えたプロピレン系ポリマー組成物 |
| CN112119119A (zh) | 2018-06-13 | 2020-12-22 | 陶氏环球技术有限责任公司 | 含有低分子量丙烯基聚合物和烯烃多嵌段共聚物的组合物 |
| KR102601945B1 (ko) | 2018-06-29 | 2023-11-16 | 다우 글로벌 테크놀로지스 엘엘씨 | 폼 비드 및 소결된 폼 구조물 |
| EP3814434B1 (en) | 2018-06-29 | 2022-07-27 | Dow Global Technologies Llc | Shelf stable aqueous dispersions suitable for use in food contact applications |
| US11702512B2 (en) | 2018-07-17 | 2023-07-18 | Dow Silicones Corporation | Polysiloxane resin-polyolefin copolymer and methods for the preparation and use thereof |
| TWI815919B (zh) | 2018-07-19 | 2023-09-21 | 美商陶氏全球科技有限責任公司 | 透氣彈性膜與層壓材料以及由其製備之製品 |
| JP7083723B2 (ja) | 2018-08-07 | 2022-06-13 | リケンテクノス株式会社 | 摺動材料組成物、摺動性成形物、および摺動性部材 |
| BR112021000591B1 (pt) | 2018-08-16 | 2023-09-26 | Dow Global Technologies Llc | Composição de enchimento intumescente, e, sistema de grama artificial |
| US12195612B2 (en) | 2018-08-31 | 2025-01-14 | Dow Global Technologies Llc | Blends for foams, foams manufactured therefrom and articles comprising the same |
| US20210252774A1 (en) | 2018-11-06 | 2021-08-19 | Dow Global Technologies Llc | Additive manufacturing with an olefin block copolymer and articles made therefrom |
| KR102880619B1 (ko) | 2018-12-28 | 2025-11-04 | 다우 글로벌 테크놀로지스 엘엘씨 | 텔레켈릭 폴리올레핀을 포함하는 경화성 조성물 |
| EP3902852A1 (en) | 2018-12-28 | 2021-11-03 | Dow Global Technologies LLC | Telechelic polyolefins and processes for preparing the same |
| JP2022516120A (ja) | 2018-12-28 | 2022-02-24 | ダウ グローバル テクノロジーズ エルエルシー | 有機金属連鎖移動剤 |
| WO2020139993A1 (en) | 2018-12-28 | 2020-07-02 | Dow Global Technologies Llc | Curable compositions comprising unsaturated polyolefins |
| SG11202107057WA (en) | 2018-12-28 | 2021-07-29 | Dow Global Technologies Llc | Curable compositions comprising unsaturated polyolefins |
| KR102829711B1 (ko) | 2019-02-12 | 2025-07-04 | 다우 글로벌 테크놀로지스 엘엘씨 | 케이블 재킷용 중합성 조성물 |
| AR118013A1 (es) | 2019-02-15 | 2021-09-08 | Dow Global Technologies Llc | Método para formar fibras elásticas y artículos estirables que contienen tales fibras |
| KR102715918B1 (ko) | 2019-03-29 | 2024-10-15 | 다우 글로벌 테크놀로지스 엘엘씨 | 열가소성 가황물을 위한 오일-증량된 펠릿 형태 에틸렌 알파-올레핀 디엔 인터폴리머 |
| WO2020212905A1 (en) | 2019-04-17 | 2020-10-22 | Nitto Denko Corporation | Multilayer co-extruded films and article containing same |
| US12325778B2 (en) | 2019-04-23 | 2025-06-10 | Northwestern University | Urethane exchange catalysts and methods for reprocessing cross-linked polyurethane foams |
| JP7654639B2 (ja) | 2019-08-29 | 2025-04-01 | ダウ グローバル テクノロジーズ エルエルシー | 改善された熱特性を有するポリマーブレンド |
| WO2021035709A1 (en) | 2019-08-30 | 2021-03-04 | Dow Global Technologies Llc | Polyolefin compositions having improved electrical properties |
| WO2021035713A1 (en) | 2019-08-30 | 2021-03-04 | Dow Global Technologies Llc | Photovoltaic encapsulant films comprising fumed alumina |
| TW202122426A (zh) | 2019-09-11 | 2021-06-16 | 南韓商Lg化學股份有限公司 | 改質之共軛二烯系聚合物、其製備方法及包含彼之橡膠組成物 |
| KR102533014B1 (ko) | 2019-09-11 | 2023-05-17 | 주식회사 엘지화학 | 변성 공액디엔계 중합체, 이의 제조방법 및 이를 포함하는 고무 조성물 |
| JP7280972B2 (ja) * | 2019-09-11 | 2023-05-24 | エルジー・ケム・リミテッド | 変性共役ジエン系重合体、その製造方法、およびそれを含むゴム組成物 |
| EP3950747B1 (en) | 2019-09-11 | 2023-08-09 | Lg Chem, Ltd. | Modified conjugated diene-based polymer and rubber composition including the same |
| EP3901187B1 (en) | 2019-09-11 | 2024-12-18 | LG Chem, Ltd. | Modified conjugated diene-based polymer and rubber composition comprising same |
| AR119924A1 (es) | 2019-09-30 | 2022-01-19 | Dow Global Technologies Llc | Película multicapa flexible |
| KR20220084062A (ko) * | 2019-09-30 | 2022-06-21 | 다우 글로벌 테크놀로지스 엘엘씨 | 폴리올레핀계 다층 탄성 필름 |
| CN114450341B (zh) | 2019-10-11 | 2024-09-27 | 陶氏环球技术有限责任公司 | 使用具有烯烃嵌段共聚物的回收聚烯烃的增材制造和由其制成的制品 |
| CN114502637A (zh) | 2019-10-18 | 2022-05-13 | 陶氏环球技术有限责任公司 | 聚烯烃丙烯酸聚合物对苯乙烯聚合物的抗冲改性 |
| WO2021080803A1 (en) | 2019-10-22 | 2021-04-29 | Exxonmobil Chemical Patents Inc. | Impact copolymer compositions |
| US20220306849A1 (en) | 2019-10-22 | 2022-09-29 | Celanese International Corporation | Thermoplastic Vulcanizate Compositions and Processes for the Production Thereof |
| CN114599738B (zh) | 2019-10-24 | 2023-09-26 | 英威达纺织(英国)有限公司 | 聚酰胺组合物及由其制成的制品 |
| CN114449912B (zh) | 2019-11-20 | 2024-08-16 | 株式会社爱世克私 | 鞋用构件和鞋 |
| CN113045816B (zh) | 2019-12-27 | 2024-01-09 | 株式会社爱世克私 | 缓冲体和鞋 |
| JP7075921B2 (ja) | 2019-12-27 | 2022-05-26 | 株式会社アシックス | 緩衝体及び靴 |
| EP4085042B1 (en) * | 2019-12-30 | 2025-09-03 | Dow Global Technologies LLC | Process for preparing an alpha-substituted acrylate |
| EP4085081A1 (en) | 2019-12-30 | 2022-11-09 | Dow Global Technologies LLC | Process for preparing an olefin-acrylate diblock copolymer |
| JP2023508013A (ja) | 2019-12-30 | 2023-02-28 | ダウ グローバル テクノロジーズ エルエルシー | アルファ-置換アクリレートを調製するためのプロセス |
| EP3910021B1 (en) | 2020-03-23 | 2025-08-20 | Sumitomo Chemical Company, Limited | Thermoplastic elastomer composition |
| TWI879942B (zh) * | 2020-04-16 | 2025-04-11 | 南韓商Lg化學股份有限公司 | 配位基化合物、過渡金屬化合物,及含彼之觸媒組成物 |
| US20230193091A1 (en) | 2020-04-29 | 2023-06-22 | Dow Global Technologies Llc | Compositions containing high melt index ethylene/alpha-olefin multi-block interpolymers |
| EP4143248A1 (en) | 2020-04-30 | 2023-03-08 | Dow Global Technologies LLC | Process for preparing olefin-acrylate block copolymers by raft polyerization |
| EP4143249A1 (en) | 2020-04-30 | 2023-03-08 | Dow Global Technologies LLC | Process for preparing olefin-acrylate block copolymers by atrp |
| JP7750859B2 (ja) * | 2020-05-07 | 2025-10-07 | ダウ グローバル テクノロジーズ エルエルシー | オレフィン重合二金属活性化剤 |
| WO2021231362A1 (en) | 2020-05-12 | 2021-11-18 | Exxonmobil Chemical Patents Inc. | Thermoplastic elastomer compositions for use in pharmaceutical articles |
| US12441873B2 (en) | 2020-05-27 | 2025-10-14 | Dow Global Technologies Llc | Polymer formulations and irrigation tubing including polymer formulations |
| WO2021242795A1 (en) * | 2020-05-29 | 2021-12-02 | Dow Global Technologies Llc | Attenuated post-metallocene catalysts |
| CN115697673A (zh) | 2020-06-19 | 2023-02-03 | 罗门哈斯公司 | 聚烯烃/(甲基)丙烯酸复合聚合物组合物及其制备方法 |
| JP7537007B2 (ja) * | 2020-08-21 | 2024-08-20 | ダウ グローバル テクノロジーズ エルエルシー | 高い体積抵抗率を有するメルトブローン不織布及びその物品 |
| US20230399450A1 (en) | 2020-11-10 | 2023-12-14 | Dow Global Technologies Llc | Preparation of non-polar-polar block copolymers via vinyl-terminated polyolefins |
| EP4244280B1 (en) | 2020-11-10 | 2024-10-30 | Dow Global Technologies LLC | Preparation of polyolefin-polyacrylate block copolymers additives for increasing surface energy of polyethylene |
| WO2022115426A1 (en) | 2020-11-24 | 2022-06-02 | Dow Global Technologies Llc | Process for producing foam article |
| JP7630623B2 (ja) | 2020-12-14 | 2025-02-17 | ダウ グローバル テクノロジーズ エルエルシー | ポリオレフィン発泡体ビーズ及びその製造方法 |
| WO2022126313A1 (en) | 2020-12-14 | 2022-06-23 | Dow Global Technologies Llc | A high energy return foam and method for preparing the same |
| CN114853964B (zh) * | 2021-02-04 | 2023-12-22 | 中国石油天然气股份有限公司 | 环烯烃嵌段共聚物及其制备方法 |
| EP4140827A1 (en) | 2021-08-26 | 2023-03-01 | Sumitomo Chemical Company, Limited | Method for producing thermoplastic elastomer composition |
| WO2023039515A2 (en) | 2021-09-10 | 2023-03-16 | Dow Global Technologies Llc | Borate cocatalysts for polyolefin production |
| KR20240052978A (ko) | 2021-09-10 | 2024-04-23 | 다우 글로벌 테크놀로지스 엘엘씨 | 올레핀 중합용 탄화수소 가용성 보레이트 공촉매 |
| JP2025505579A (ja) | 2022-02-09 | 2025-02-28 | ダウ グローバル テクノロジーズ エルエルシー | 3dループ製品及びそれを調製するための方法 |
| WO2023205747A1 (en) * | 2022-04-20 | 2023-10-26 | Northwestern University | Synthesis of copolymers from homopolymers |
| CN114958471A (zh) * | 2022-07-01 | 2022-08-30 | 重庆合晶能源科技有限公司 | 一种电机变速箱油及其制备方法 |
| JP2025524635A (ja) | 2022-07-15 | 2025-07-30 | ダウ グローバル テクノロジーズ エルエルシー | 可逆的架橋発泡体物品及びプロセス |
| EP4543942A1 (en) | 2022-07-15 | 2025-04-30 | Dow Global Technologies LLC | Ethylene-based polymer with reversible crosslinker |
| CN119894975A (zh) | 2022-09-30 | 2025-04-25 | 陶氏环球技术有限责任公司 | 具有优异冲击强度和透光率的聚烯烃组合物 |
| CN115779962B (zh) * | 2022-10-19 | 2024-04-05 | 浙江大学 | 一种氢键供体-亲核双功能试剂和有机硼试剂组成的双组分有机催化体系及其应用 |
| WO2025005968A1 (en) | 2023-06-27 | 2025-01-02 | Dow Global Technologies Llc | Multi stage process for producing ethylene-based polymer with (ultra) high molecular weight polyethylene component |
| WO2025019115A1 (en) | 2023-07-20 | 2025-01-23 | Dow Global Technologies Llc | Spunbond nonwoven comprising a mixture of fibers |
| WO2025072678A1 (en) | 2023-09-29 | 2025-04-03 | Dow Global Technologies Llc | Process for preparing an olefin-acrylate block copolymer |
| WO2025096015A1 (en) | 2023-10-30 | 2025-05-08 | Dow Global Technologies Llc | Bicomponent fiber |
| WO2025096765A1 (en) | 2023-10-31 | 2025-05-08 | Dow Global Technologies Llc | Ethylene-based polymer compositions for tpo applications |
| EP4596232A1 (en) | 2024-01-31 | 2025-08-06 | Dow Global Technologies LLC | Tie layers comprising crystalline block composite components and functionalized polyethylene and coated substrates incorporating same |
| EP4596231A1 (en) | 2024-01-31 | 2025-08-06 | Dow Global Technologies LLC | Tie layers comprising crystalline block composite components and functionalized polyethylene and multilayer films incorporating same |
| WO2025171254A1 (en) * | 2024-02-09 | 2025-08-14 | Dow Global Technologies Llc | Catalysts for gas phase polymerization and process |
| WO2025207892A1 (en) | 2024-03-28 | 2025-10-02 | Dow Global Technologies Llc | Olefin-based polymer compositions with good impact performance, stiffness and light transmittance |
| WO2025244992A1 (en) | 2024-05-21 | 2025-11-27 | Dow Global Technologies Llc | Crosslinked compositions with ethylene-based polymer and reversible crosslinker |
| CN119955040B (zh) * | 2024-12-20 | 2025-10-17 | 浙江大学 | 一种共聚单体含量梯级分布的嵌段共聚物制备方法 |
| CN119978270A (zh) * | 2025-01-03 | 2025-05-13 | 浙江大学宁波“五位一体”校区教育发展中心 | 一种基于多反应器工艺制备多嵌段且共聚单体含量梯级分布的嵌段共聚物的方法 |
Family Cites Families (169)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2973344A (en) | 1957-12-11 | 1961-02-28 | Exxon Research Engineering Co | Modified polymers |
| US4039632A (en) | 1958-01-16 | 1977-08-02 | Phillips Petroleum Company | Preparation of block copolymers |
| US3970719A (en) | 1958-01-16 | 1976-07-20 | Phillips Petroleum Company | Preparation of block copolymers |
| US2997432A (en) | 1958-08-14 | 1961-08-22 | Phillips Petroleum Co | Dyeing of 1-olefin polymers |
| US3873642A (en) | 1961-02-20 | 1975-03-25 | Avisun Corp | Crystalline olefin block polymers and their preparation |
| US3360599A (en) * | 1963-11-06 | 1967-12-26 | Shell Oil Co | Preparation of coherent block copolymer films of high tensile strength and extensibility |
| GB1234034A (enExample) * | 1967-08-31 | 1971-06-03 | ||
| US3649579A (en) * | 1969-01-27 | 1972-03-14 | Minnesota Mining & Mfg | Block copolymer compositions |
| US3947368A (en) * | 1971-02-25 | 1976-03-30 | Texaco Inc. | Lubricating oil compositions |
| JPS5643862B2 (enExample) | 1973-07-27 | 1981-10-15 | ||
| US4146492A (en) | 1976-04-02 | 1979-03-27 | Texaco Inc. | Lubricant compositions which exhibit low degree of haze and methods of preparing same |
| US4299931A (en) | 1980-03-10 | 1981-11-10 | Monsanto Company | Compatibilized polymer blends |
| JPS5734145A (en) | 1980-08-07 | 1982-02-24 | Mitsui Petrochem Ind Ltd | Ethylene-alpha-olefin copolymer composition |
| JPS5975929A (ja) | 1982-10-25 | 1984-04-28 | Sekisui Chem Co Ltd | ポリオレフイン発泡体の製造方法 |
| JPH0610269B2 (ja) * | 1983-05-12 | 1994-02-09 | 鐘淵化学工業株式会社 | ポリオレフィン系樹脂発泡粒子およびその製法 |
| JPS6088016A (ja) * | 1983-10-21 | 1985-05-17 | Mitsui Petrochem Ind Ltd | エチレン共重合体 |
| JPS60228552A (ja) * | 1984-04-27 | 1985-11-13 | Ube Ind Ltd | ガラス繊維強化ポリプロピレン組成物 |
| CA1264880A (en) | 1984-07-06 | 1990-01-23 | John Brooke Gardiner | Viscosity index improver - dispersant additive useful in oil compositions |
| ES8705288A1 (es) | 1985-07-03 | 1987-05-01 | Ver Edelstahlwerke Ag | Dispositivo para moldeo asistido por presion en particular,fundicion inyectada de cuerpos moldeados. |
| US4798081A (en) | 1985-11-27 | 1989-01-17 | The Dow Chemical Company | High temperature continuous viscometry coupled with analytic temperature rising elution fractionation for evaluating crystalline and semi-crystalline polymers |
| DE3784235T2 (de) | 1986-12-26 | 1993-09-09 | Mitsubishi Petrochemical Co | Verfahren zur herstellung vernetzter blockcopolymere von olefinen. |
| US5391629A (en) | 1987-01-30 | 1995-02-21 | Exxon Chemical Patents Inc. | Block copolymers from ionic catalysts |
| CA1318734C (en) | 1987-11-20 | 1993-06-01 | Mitsuyuki Okada | Modified polyolefin resin |
| US5266626A (en) | 1989-02-22 | 1993-11-30 | Norsolor | Thermoplastic elastomer based on an ethylene/α-olefin copolymer and on polynorbornene |
| US5270410A (en) | 1989-04-25 | 1993-12-14 | Shell Oil Company | Process for the production of elastomeric, primarily syndiotactic polypropylene and catalysts for use in said process |
| US5270276A (en) | 1989-04-25 | 1993-12-14 | Shell Oil Company | Process for the production of elastomeric, primarily syndiotactic polypropylene and catalysts for use in said process |
| US4971936A (en) | 1989-07-10 | 1990-11-20 | Shell Oil Company | Catalyst component for making primarily isotactic elastomeric polypropylene or polybutene |
| US6025448A (en) | 1989-08-31 | 2000-02-15 | The Dow Chemical Company | Gas phase polymerization of olefins |
| US5068047A (en) | 1989-10-12 | 1991-11-26 | Exxon Chemical Patents, Inc. | Visosity index improver |
| JP2831779B2 (ja) * | 1990-02-01 | 1998-12-02 | 旭電化工業株式会社 | ポリオレフィン樹脂組成物 |
| DE69128028T2 (de) * | 1990-02-09 | 1998-06-10 | Exxon Chemical Patents Inc | Blockcopolymere von ionischen katalysatoren |
| GB2241244B (en) | 1990-02-22 | 1994-07-06 | James C W Chien | Thermoplastic elastomers |
| US5089573A (en) | 1990-02-26 | 1992-02-18 | Shell Oil Company | Process for the production of elastomeric, primarily isotactic polyolefins and catalysts for use in said process |
| US5118767A (en) | 1990-02-26 | 1992-06-02 | Shell Oil Company | Process for producing mildly elastomeric primarily isotatic polypropylene and poly-1-butene |
| US5118768A (en) | 1990-05-11 | 1992-06-02 | Shell Oil Company | Process for the production of elastomeric, primarily isotactic polyolefins and catalysts for use in said process |
| ATE143984T1 (de) * | 1990-07-16 | 1996-10-15 | Basf Ag | Gepfropfte und vernetzte propylencopolymerisate |
| US5134209A (en) | 1990-12-26 | 1992-07-28 | Shell Oil Company | Process of producing ethylene-propylene rubbery copolymer |
| US5229477A (en) | 1991-08-26 | 1993-07-20 | Shell Oil Company | Process for producing ethylene-propylene-diene monomer terpolymer |
| US5783638A (en) | 1991-10-15 | 1998-07-21 | The Dow Chemical Company | Elastic substantially linear ethylene polymers |
| US5210338A (en) | 1991-10-25 | 1993-05-11 | Ethyl Corporation | Catalyzed chain growth process |
| ES2095037T3 (es) | 1991-12-30 | 1997-02-01 | Dow Chemical Co | Polimerizaciones de interpolimeros de etileno. |
| US5276220A (en) | 1992-06-18 | 1994-01-04 | Ethyl Corporation | Actinide catalyzed chain growth process |
| TW272985B (enExample) | 1992-09-11 | 1996-03-21 | Hoechst Ag | |
| DE69322871T2 (de) | 1992-09-15 | 1999-05-12 | The Dow Chemical Co., Midland, Mich. | Schlagzähmodifizierung von thermoplastiken |
| US5322728A (en) * | 1992-11-24 | 1994-06-21 | Exxon Chemical Patents, Inc. | Fibers of polyolefin polymers |
| TW275076B (enExample) | 1992-12-02 | 1996-05-01 | Hoechst Ag | |
| 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. |
| JPH0790035A (ja) | 1993-07-27 | 1995-04-04 | Ube Ind Ltd | プロピレンブロック共重合体の製造方法 |
| JP3031142B2 (ja) | 1993-11-01 | 2000-04-10 | 住友化学工業株式会社 | ポリプロピレン樹脂組成物 |
| CN1068017C (zh) | 1993-11-12 | 2001-07-04 | 钟渊化学工业株式会社 | 聚烯烃类树脂组合物 |
| US5594080A (en) | 1994-03-24 | 1997-01-14 | Leland Stanford, Jr. University | Thermoplastic elastomeric olefin polymers, method of production and catalysts therefor |
| EP0758348B1 (en) | 1994-04-06 | 1999-07-14 | Infineum USA L.P. | Ethylene alpha-olefin block copolymers and methods for production thereof |
| RU2149878C1 (ru) | 1994-04-06 | 2000-05-27 | Эксон Кемикэл Пейтентс Инк. | ЭТИЛЕН-α-ОЛЕФИНОВЫЕ БЛОК-СОПОЛИМЕРЫ И СПОСОБЫ ИХ ПОЛУЧЕНИЯ |
| DE4425408A1 (de) | 1994-07-13 | 1996-01-18 | Hoechst Ag | Cycloolefinpolymere |
| CA2183465A1 (en) * | 1995-01-23 | 1996-08-01 | Kazuyuki Watanabe | Propylene resin composition and molded article thereof |
| US5543458A (en) | 1995-01-31 | 1996-08-06 | Shell Oil Company | Process for making graft block copolymers by growing anionic polymer chains from functionalized polyolefin backbones |
| US5550194A (en) | 1995-01-31 | 1996-08-27 | Shell Oil Company | Process for making graft block copolymers by grafting anionic polymer chains onto functionalized polyolefins |
| US5693713A (en) | 1995-05-30 | 1997-12-02 | Shell Oil Company | Process for making block graft copolymers by grafting halosilanes onto polyolefin/diene polymers |
| KR19990064042A (ko) | 1995-10-06 | 1999-07-26 | 그레이스 스티븐 에스. | 측쇄형 블록 에틸렌 중합체, 이의 제조방법및 이를 포함하는조성물 |
| US6051681A (en) | 1995-11-17 | 2000-04-18 | Dsm N.V. | Process for the preparation of a thermoplastic elastomer |
| ID17196A (id) * | 1996-03-14 | 1997-12-11 | Dow Chemical Co | Bahan-bahan perekat yang mengandung polimer-polimer 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 |
| EP0886669B1 (en) | 1996-03-15 | 2000-05-10 | Amoco Corporation | Stiff, strong, tough glass-filled olefin polymer |
| AU3603797A (en) | 1996-03-27 | 1997-10-17 | Dow Chemical Company, The | Allyl containing metal complexes and olefin polymerization process |
| HU223533B1 (hu) * | 1996-06-17 | 2004-08-30 | Exxonmobil Chemical Patents Inc. | Vegyes átmenetifém katalizátor-rendszer olefinek polimerizálására |
| CA2262468A1 (en) | 1996-09-04 | 1998-03-12 | Exxon Chemical Patents, Inc. | Improved propylene polymers for oriented films |
| US6177377B1 (en) * | 1996-12-18 | 2001-01-23 | Amherst Polymer Technology, Inc. | Polymer blends and process for preparation |
| US6362252B1 (en) | 1996-12-23 | 2002-03-26 | Vladimir Prutkin | Highly filled polymer composition with improved properties |
| CN1130406C (zh) | 1997-02-07 | 2003-12-10 | 埃克森美孚化学专利公司 | 结合有聚乙烯大分子单体的丙烯聚合物 |
| US6114457A (en) | 1997-02-07 | 2000-09-05 | Exxon Chemical Patents Inc. | High melt strength polyethylene compositions |
| US5783531A (en) | 1997-03-28 | 1998-07-21 | Exxon Research And Engineering Company | Manufacturing method for the production of polyalphaolefin based synthetic greases (LAW500) |
| AR012645A1 (es) * | 1997-05-01 | 2000-11-08 | Dow Global Technologies Inc | Polimeros de alfa-olefinas preparados por polimerizacion en presencia de complejos de metales que contienen grupos indenilo |
| WO1998057996A1 (en) | 1997-06-14 | 1998-12-23 | The Board Of Trustees Of The Leland Stanford, Jr. University | ETHYLENE ENHANCEMENT OF PROCESSES FOR SYNTHESIS OF HIGH MELTING THERMOPLASTIC ELASTOMERIC α-OLEFIN POLYMERS (PRE/EPE EFFECTS) |
| US6143828A (en) * | 1997-06-14 | 2000-11-07 | Honam Petrochemical Corporation | Olefin-based crosslinked thermoplastic elastomers and a process of preparation thereof |
| ID24299A (id) | 1997-08-08 | 2000-07-13 | Dow Chemical Co | Bahan lembaran yang sesuai digunakan sebagai bahan penutup lantai, dinding atau langit-langit, dan proses-proses dan zat perantara untuk pembuatannya |
| US6096668A (en) | 1997-09-15 | 2000-08-01 | Kimberly-Clark Worldwide, Inc. | Elastic film laminates |
| AR012518A1 (es) | 1997-09-19 | 2000-10-18 | Dow Global Technologies Inc | Composicion de polimeros que comprende etileno interpolimerizado con al menos un comonomero insaturado, proceso para prepararla y articulo fabricado que la comprende |
| US6197404B1 (en) | 1997-10-31 | 2001-03-06 | Kimberly-Clark Worldwide, Inc. | Creped nonwoven materials |
| US6380341B1 (en) | 1998-01-09 | 2002-04-30 | The Board Of Trustees Of Leland Stanford Jr. University | Ethylene copolymers with narrow composition distribution and high melting temperatures, and methods of production thereof |
| AU2111599A (en) | 1998-01-09 | 1999-07-26 | Board Of Trustees Of The Leland Stanford Junior University | High-melting polyolefin copolymer elastomers, catalysts and methods of synthesis |
| WO1999035171A1 (en) | 1998-01-09 | 1999-07-15 | The Board Of Trustees Of The Leland Stanford Jr. University | High-melting polyolefin copolymer elastomers, catalysts and methods of synthesis |
| JPH11279216A (ja) * | 1998-03-25 | 1999-10-12 | Sumitomo Chem Co Ltd | オレフィン重合体の製造方法 |
| US6815023B1 (en) | 1998-07-07 | 2004-11-09 | Curwood, Inc. | Puncture resistant polymeric films, blends and process |
| US6322728B1 (en) | 1998-07-10 | 2001-11-27 | Jeneric/Pentron, Inc. | Mass production of dental restorations by solid free-form fabrication methods |
| EP1829907B1 (en) * | 1998-10-19 | 2012-04-11 | JNC Petrochemical Corporation | Propylene/ethylene block copolymer, blushing-resistant transparent polypropylene resin for molding, elastomer for molding, and molded article obtained therefrom |
| EP1141051B1 (en) | 1998-12-21 | 2008-01-23 | ExxonMobil Chemical Patents Inc. | Process to prepare branched ethylene-propylene copolymers |
| KR100565151B1 (ko) | 1999-02-04 | 2006-03-30 | 미쓰이 가가쿠 가부시키가이샤 | 폴리프로필렌 블록 공중합체 수지 및 제조 방법 |
| US6680265B1 (en) | 1999-02-22 | 2004-01-20 | Kimberly-Clark Worldwide, Inc. | Laminates of elastomeric and non-elastomeric polyolefin blend materials |
| CA2388137A1 (en) * | 1999-10-22 | 2001-05-03 | Univation Technologies, Llc | Catalyst compositions, methods of polymerization, and polymers therefrom |
| CN1253498C (zh) * | 1999-11-12 | 2006-04-26 | 积水化学工业株式会社 | 聚烯烃树脂组合物 |
| US6340730B1 (en) | 1999-12-06 | 2002-01-22 | Univation Technologies, Llc | Multiple catalyst system |
| US6323284B1 (en) * | 1999-12-10 | 2001-11-27 | Exxonmobil Chemical Patents, Inc. | Method of preparation of crosslinked blends of amorphous and crystalline polymers |
| EP2267042B1 (en) * | 2000-01-26 | 2015-06-10 | Mitsui Chemicals, Inc. | Olefin diblock copolymer of very low polydispersity and process for preparing the same |
| US6537472B2 (en) | 2000-02-29 | 2003-03-25 | Asahi Kasei Kabushiki Kaisha | Process for producing a cushioning article |
| US6160029A (en) | 2000-03-08 | 2000-12-12 | The Dow Chemical Company | Olefin polymer and α-olefin/vinyl or α-olefin/vinylidene interpolymer blend foams |
| US6455638B2 (en) | 2000-05-11 | 2002-09-24 | Dupont Dow Elastomers L.L.C. | Ethylene/α-olefin polymer blends comprising components with differing ethylene contents |
| KR100745227B1 (ko) | 2000-05-26 | 2007-08-01 | 다우 글로벌 테크놀로지스 인크. | 폴리에틸렌 풍부/폴리프로필렌 블렌드 및 그의 용도 |
| NO20013880L (no) * | 2000-08-22 | 2002-02-25 | Rohm & Haas | Matriks og fremgangsmåte for fremstilling av polyolefiner |
| JP2002206007A (ja) | 2000-11-08 | 2002-07-26 | National Institute Of Advanced Industrial & Technology | オレフィン系ブロック共重合体の製法 |
| US6429175B1 (en) * | 2000-11-20 | 2002-08-06 | New Age Chemical, Inc. | Lubricating grease composition |
| WO2002046246A2 (en) | 2000-12-04 | 2002-06-13 | Univaton Technologies, Llc | Polimerization process |
| EP1373367A2 (en) | 2001-01-10 | 2004-01-02 | Basell Poliolefine Italia S.p.A. | Block copolymers and process for their preparation |
| MY131000A (en) | 2001-03-16 | 2007-07-31 | Dow Global Technologies Inc | High melt strength polymers and method of making same |
| US20040092662A1 (en) | 2001-03-29 | 2004-05-13 | Yasuhiro Goto | Propylene polymer composition, molded object, and polyolefin copolymer |
| US6444867B1 (en) | 2001-05-17 | 2002-09-03 | Bp Corporation North America Inc. | Process for linear alpha olefins |
| SG120869A1 (en) | 2001-05-31 | 2006-04-26 | Mitsui Chemicals Inc | Olefin block copolymer, viscosity index improver for lubricating oils and lubricating oil composition |
| US7022766B2 (en) | 2001-05-31 | 2006-04-04 | Mitsui Chemicals, Inc. | Olefin block copolymer, viscosity index improver for lubricating oils and lubricating oil composition |
| DE10127926A1 (de) | 2001-06-08 | 2002-12-12 | Bayer Ag | 1,3-disubstituierte Indenkomplexe |
| JP4178404B2 (ja) | 2001-06-29 | 2008-11-12 | 東洋化成工業株式会社 | バインダー樹脂溶液組成物、塗料、インキ、接着剤およびプライマー |
| US7087686B2 (en) | 2001-08-06 | 2006-08-08 | Bp Chemicals Limited | Chain growth reaction process |
| WO2003022890A1 (en) * | 2001-09-11 | 2003-03-20 | Exxonmobil Chemical Patents Inc. | Method for preparing polyolefins |
| DE60212544T2 (de) * | 2001-11-01 | 2007-06-06 | Mitsubishi Chemical Corp. | Modifiziertes Propylenpolymer, davon erhältliche Klebstoffzusammensetzung und Klebstoff, der dieses umfasst |
| EP1444276A1 (en) | 2001-11-06 | 2004-08-11 | Dow Global Technologies, Inc. | Isotactic propylene copolymers, their preparation and use |
| WO2003040204A1 (en) | 2001-11-09 | 2003-05-15 | Japan Polypropylene Corporation | Propylene block copolymer |
| US7005395B2 (en) | 2002-12-12 | 2006-02-28 | Invista North America S.A.R.L. | Stretchable composite sheets and processes for making |
| DE60328582D1 (de) * | 2002-01-31 | 2009-09-10 | Mitsubishi Chem Corp | Nichtsteife propylenharzzusammensetzung |
| US6992049B2 (en) | 2002-01-31 | 2006-01-31 | Exxonmobil Research And Engineering Company | Lubricating oil compositions |
| US6875828B2 (en) * | 2002-09-04 | 2005-04-05 | Univation Technologies, Llc | Bimodal polyolefin production process and films therefrom |
| AU2003272714A1 (en) | 2002-10-02 | 2004-04-23 | Dow Global Technologies Inc. | POLYMER COMPOSITIONS COMPRISING A LOW VISCOSITY, HOMOGENEOUSLY BRANCHED ETHYLENE/Alpha-OLEFIN EXTENDER |
| EP2261292B1 (en) | 2002-10-15 | 2014-07-23 | ExxonMobil Chemical Patents Inc. | Polyolefin adhesive compositions |
| JP2004204058A (ja) | 2002-12-25 | 2004-07-22 | Mitsui Chemicals Inc | オレフィン系ブロック共重合体 |
| US6759474B1 (en) * | 2003-03-03 | 2004-07-06 | Ferro Corporation | Glass reinforced nylon blend with improved knitline strength |
| US20050039634A1 (en) * | 2003-07-11 | 2005-02-24 | Hermansky Clarence Gaetano | Non-aqueous ink jet inks with improved decap |
| CA2553675A1 (en) | 2004-01-22 | 2005-08-11 | Dow Global Technologies Inc. | Functionalized elastomer compositions |
| US7608668B2 (en) * | 2004-03-17 | 2009-10-27 | Dow Global Technologies Inc. | Ethylene/α-olefins block interpolymers |
| US7355089B2 (en) * | 2004-03-17 | 2008-04-08 | Dow Global Technologies Inc. | Compositions of ethylene/α-olefin multi-block interpolymer for elastic films and laminates |
| US7741397B2 (en) * | 2004-03-17 | 2010-06-22 | Dow Global Technologies, Inc. | Filled polymer compositions made from interpolymers of ethylene/α-olefins and uses thereof |
| US7622529B2 (en) * | 2004-03-17 | 2009-11-24 | Dow Global Technologies Inc. | Polymer blends from interpolymers of ethylene/alpha-olefin with improved compatibility |
| US7557147B2 (en) * | 2004-03-17 | 2009-07-07 | Dow Global Technologies Inc. | Soft foams made from interpolymers of ethylene/alpha-olefins |
| JP4879882B2 (ja) | 2004-03-17 | 2012-02-22 | ダウ グローバル テクノロジーズ エルエルシー | より高次のオレフィンマルチブロックコポリマーを形成するためのシャトリング剤を含む触媒組成物 |
| US7714071B2 (en) * | 2004-03-17 | 2010-05-11 | Dow Global Technologies Inc. | Polymer blends from interpolymers of ethylene/α-olefins and flexible molded articles made therefrom |
| US7863379B2 (en) * | 2004-03-17 | 2011-01-04 | Dow Global Technologies Inc. | Impact modification of thermoplastics with ethylene/alpha-olefin interpolymers |
| US7671131B2 (en) * | 2004-03-17 | 2010-03-02 | Dow Global Technologies Inc. | Interpolymers of ethylene/α-olefins blends and profiles and gaskets made therefrom |
| US7803728B2 (en) * | 2004-03-17 | 2010-09-28 | Dow Global Technologies Inc. | Fibers made from copolymers of ethylene/α-olefins |
| US8273826B2 (en) * | 2006-03-15 | 2012-09-25 | Dow Global Technologies Llc | Impact modification of thermoplastics with ethylene/α-olefin interpolymers |
| JP5133050B2 (ja) * | 2004-03-17 | 2013-01-30 | ダウ グローバル テクノロジーズ エルエルシー | エチレンマルチブロックコポリマーを形成するためのシャトリング剤を含む触媒組成物 |
| KR101277095B1 (ko) | 2004-03-17 | 2013-06-20 | 다우 글로벌 테크놀로지스 엘엘씨 | 셔틀링제를 포함하는, 에틸렌 공중합체 형성용 촉매 조성물 |
| US7897689B2 (en) * | 2004-03-17 | 2011-03-01 | Dow Global Technologies Inc. | Functionalized ethylene/α-olefin interpolymer compositions |
| US7666918B2 (en) * | 2004-03-17 | 2010-02-23 | Dow Global Technologies, Inc. | Foams made from interpolymers of ethylene/α-olefins |
| US7662881B2 (en) * | 2004-03-17 | 2010-02-16 | Dow Global Technologies Inc. | Viscosity index improver for lubricant compositions |
| US7795321B2 (en) * | 2004-03-17 | 2010-09-14 | Dow Global Technologies Inc. | Rheology modification of interpolymers of ethylene/α-olefins and articles made therefrom |
| US8816006B2 (en) * | 2004-03-17 | 2014-08-26 | Dow Global Technologies Llc | Compositions of ethylene/α-olefin multi-block interpolymer suitable for films |
| US7514517B2 (en) * | 2004-03-17 | 2009-04-07 | Dow Global Technologies Inc. | Anti-blocking compositions comprising interpolymers of ethylene/α-olefins |
| US7582716B2 (en) * | 2004-03-17 | 2009-09-01 | Dow Global Technologies Inc. | Compositions of ethylene/α-olefin multi-block interpolymer for blown films with high hot tack |
| US7524911B2 (en) * | 2004-03-17 | 2009-04-28 | Dow Global Technologies Inc. | Adhesive and marking compositions made from interpolymers of ethylene/α-olefins |
| US7579408B2 (en) * | 2004-03-17 | 2009-08-25 | Dow Global Technologies Inc. | Thermoplastic vulcanizate comprising interpolymers of ethylene/α-olefins |
| US7504347B2 (en) * | 2004-03-17 | 2009-03-17 | Dow Global Technologies Inc. | Fibers made from copolymers of propylene/α-olefins |
| AU2005224677A1 (en) | 2004-03-19 | 2005-09-29 | Dow Global Technologies Inc. | Propylene-based copolymers, a method of making the fibers and articles made from the fibers |
| JP2008509277A (ja) | 2004-08-09 | 2008-03-27 | ダウ グローバル テクノロジーズ インコーポレイティド | ポリマーの製造のための担持ビス(ヒドロキシアリールアリールオキシ)触媒 |
| US8084537B2 (en) * | 2005-03-17 | 2011-12-27 | Dow Global Technologies Llc | Polymer blends from interpolymers of ethylene/α-olefin with improved compatibility |
| US7910658B2 (en) * | 2005-03-17 | 2011-03-22 | Dow Global Technologies Llc | Compositions of ethylene/α-olefin multi-block interpolymer for elastic films and laminates |
| EP1869095B1 (en) * | 2005-03-17 | 2011-04-27 | Dow Global Technologies LLC | Compositions of ethylene/alpha-olefin multi-block interpolymer for elastic films and laminates |
| CA2601376A1 (en) * | 2005-03-17 | 2006-09-28 | Dow Global Technologies Inc. | Fibers made from copolymers of ethylene/alpha-olefins |
| US7737215B2 (en) * | 2005-03-17 | 2010-06-15 | Dow Global Technologies Inc. | Compositions of ethylene/α-olefin multi-block interpolymer for elastic films and laminates |
| US7786216B2 (en) * | 2005-03-17 | 2010-08-31 | Dow Global Technologies Inc. | Oil based blends of interpolymers of ethylene/α-olefins |
| MY158058A (en) * | 2005-03-17 | 2016-08-30 | Dow Global Technologies Inc | ADHESIVE AND MARKING COMPOSITIONS MADE FROM INTERPOLYMERS OF ETHYLENE/a-OLEFINS |
| TW200722441A (en) * | 2005-09-15 | 2007-06-16 | Dow Global Technologies Inc | Catalytic olefin block copolymers via polymerizable shuttling agent |
| US7906587B2 (en) * | 2005-09-16 | 2011-03-15 | Dow Global Technologies Llc | Polymer blends from interpolymer of ethylene/α olefin with improved compatibility |
| EP3428329B1 (en) * | 2005-10-26 | 2020-11-25 | Dow Global Technologies LLC | A fiber comprising a low crystallinity polymer and a high crystallinity polymer |
| EP2079322A1 (en) | 2006-10-18 | 2009-07-22 | Symrise GmbH & Co. KG | Substituted bicycloý4.1.0¨heptane-7-carboxylic acid amides and derivatives thereof as food flavor substances |
| US7928022B2 (en) | 2006-11-30 | 2011-04-19 | Dow Global Technologies Llc | Olefin block compositions for heavy weight stretch fabrics |
| KR101458236B1 (ko) * | 2006-12-21 | 2014-11-04 | 다우 글로벌 테크놀로지스 엘엘씨 | 관능화된 올레핀 중합체, 조성물 및 그로부터 제조된 물품, 및 그의 제조 방법 |
| CN101981074A (zh) * | 2008-01-30 | 2011-02-23 | 陶氏环球技术公司 | 丁烯/α-烯烃嵌段互聚物 |
| WO2009097525A1 (en) * | 2008-01-30 | 2009-08-06 | Dow Global Technologies Inc. | PROPYLENE/α-OLEFIN BLOCK INTERPOLYMERS |
| CN105001584A (zh) * | 2008-01-30 | 2015-10-28 | 陶氏环球技术有限责任公司 | 乙烯/α-烯烃嵌段互聚物 |
| EP2238186B1 (en) * | 2008-01-30 | 2018-11-28 | Dow Global Technologies LLC | Ethylene/alpha-olefin block interpolymers |
| WO2009097532A1 (en) * | 2008-01-30 | 2009-08-06 | Dow Global Technologies Inc. | BUTENE/α-OLEFIN BLOCK INTERPOLYMERS |
| EP2238203B1 (en) * | 2008-01-30 | 2018-12-26 | Dow Global Technologies LLC | Propylene/ alpha-olefin block interpolymers |
| CN102239213A (zh) * | 2008-10-03 | 2011-11-09 | 陶氏环球技术有限责任公司 | 具有乙烯/α-烯烃互聚物的聚合物共混物 |
-
2005
- 2005-03-17 JP JP2007504111A patent/JP5133050B2/ja not_active Expired - Lifetime
- 2005-03-17 AT AT05730993T patent/ATE461231T1/de not_active IP Right Cessation
- 2005-03-17 WO PCT/US2005/008917 patent/WO2005090427A2/en not_active Ceased
- 2005-03-17 US US10/589,377 patent/US7858706B2/en active Active
- 2005-03-17 EP EP05730993A patent/EP1727841B1/en not_active Expired - Lifetime
- 2005-03-17 CN CN2005800148192A patent/CN1976965B/zh not_active Expired - Lifetime
- 2005-03-17 NZ NZ549261A patent/NZ549261A/en unknown
- 2005-03-17 BR BRPI0508148-3A patent/BRPI0508148B1/pt active IP Right Grant
- 2005-03-17 DE DE602005019988T patent/DE602005019988D1/de not_active Expired - Lifetime
- 2005-03-17 CA CA2559576A patent/CA2559576C/en not_active Expired - Fee Related
- 2005-03-17 AU AU2005224259A patent/AU2005224259B2/en not_active Ceased
-
2006
- 2006-08-28 ZA ZA2006/07170A patent/ZA200607170B/en unknown
- 2006-09-13 NO NO20064122A patent/NO20064122L/no not_active Application Discontinuation
-
2010
- 2010-12-08 US US12/962,822 patent/US8198374B2/en active Active
- 2010-12-08 US US12/962,800 patent/US8785551B2/en not_active Expired - Lifetime
-
2011
- 2011-02-21 US US13/031,339 patent/US8318864B2/en not_active Expired - Lifetime
-
2012
- 2012-07-31 US US13/562,600 patent/US8710143B2/en not_active Expired - Lifetime
- 2012-11-21 US US13/683,596 patent/US8609779B2/en not_active Expired - Lifetime
-
2014
- 2014-05-15 US US14/278,472 patent/US9243090B2/en not_active Expired - Lifetime
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA2559576C (en) | Catalyst composition comprising shuttling agent for ethylene multi-block copolymer formation | |
| EP2357203B1 (en) | Catalyst composition comprising shuttling agent for higher olefin multi-block copolymer formation | |
| EP2221329B1 (en) | Catalyst composition comprising shuttling agent for ethylene multi-block copolymer formation | |
| EP1926763B1 (en) | Catalytic olefin block copolymers with controlled block sequence distribution | |
| EP1861440B1 (en) | Pseudo-block copolymers and process employing chain shuttling agent | |
| HK1098771B (en) | Catalyst composition comprising shuttling agent for ethylene multi-block copolymer formation | |
| HK1115891B (en) | Pseudo-block copolymers and process employing chain shuttling agent | |
| MXPA06010584A (en) | Catalyst composition comprising shuttling agent for ethylene multi-block copolymer formation |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| MKLA | Lapsed |
Effective date: 20150317 |