CN101319050A - 包含全同立构丙烯共聚物的膜 - Google Patents
包含全同立构丙烯共聚物的膜 Download PDFInfo
- Publication number
- CN101319050A CN101319050A CN200810131873.0A CN200810131873A CN101319050A CN 101319050 A CN101319050 A CN 101319050A CN 200810131873 A CN200810131873 A CN 200810131873A CN 101319050 A CN101319050 A CN 101319050A
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- CN
- China
- Prior art keywords
- multipolymer
- catalyzer
- polymkeric substance
- alkyl
- propylene
- 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.)
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- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 title claims abstract description 115
- 229920001577 copolymer Polymers 0.000 title abstract description 41
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 151
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims abstract description 106
- 239000000203 mixture Substances 0.000 claims abstract description 98
- 239000000126 substance Substances 0.000 claims description 195
- 238000002360 preparation method Methods 0.000 claims description 61
- 239000000178 monomer Substances 0.000 claims description 42
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 claims description 16
- 239000013078 crystal Substances 0.000 claims description 6
- 238000001938 differential scanning calorimetry curve Methods 0.000 claims description 6
- 229920001169 thermoplastic Polymers 0.000 claims description 6
- 239000011954 Ziegler–Natta catalyst Substances 0.000 claims description 5
- 238000002441 X-ray diffraction Methods 0.000 claims description 3
- -1 styrene compound Chemical class 0.000 abstract description 142
- 229920000642 polymer Polymers 0.000 abstract description 81
- 239000005977 Ethylene Substances 0.000 abstract description 77
- 230000014509 gene expression Effects 0.000 abstract description 30
- 239000004711 α-olefin Substances 0.000 abstract description 25
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract description 8
- 125000000217 alkyl group Chemical group 0.000 description 99
- 238000000034 method Methods 0.000 description 99
- 125000001072 heteroaryl group Chemical group 0.000 description 90
- 239000003054 catalyst Substances 0.000 description 85
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical class CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 71
- 229910052751 metal Inorganic materials 0.000 description 65
- 239000000523 sample Substances 0.000 description 65
- 125000003118 aryl group Chemical class 0.000 description 56
- 239000002184 metal Substances 0.000 description 50
- 229920001155 polypropylene Polymers 0.000 description 48
- 239000003446 ligand Substances 0.000 description 47
- 229920001038 ethylene copolymer Polymers 0.000 description 40
- 239000000047 product Substances 0.000 description 40
- 239000000243 solution Substances 0.000 description 40
- 125000003107 substituted aryl group Chemical group 0.000 description 39
- 230000004927 fusion Effects 0.000 description 38
- 238000002844 melting Methods 0.000 description 38
- 230000008018 melting Effects 0.000 description 38
- 125000000547 substituted alkyl group Chemical group 0.000 description 38
- 125000000753 cycloalkyl group Chemical group 0.000 description 37
- 238000005516 engineering process Methods 0.000 description 36
- 230000006399 behavior Effects 0.000 description 35
- 238000006116 polymerization reaction Methods 0.000 description 35
- 230000008569 process Effects 0.000 description 35
- 239000000463 material Substances 0.000 description 34
- 150000001875 compounds Chemical class 0.000 description 33
- 239000001257 hydrogen Substances 0.000 description 33
- 229910052739 hydrogen Inorganic materials 0.000 description 33
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 32
- 125000004415 heterocyclylalkyl group Chemical group 0.000 description 32
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 31
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 description 31
- 125000003545 alkoxy group Chemical group 0.000 description 30
- 238000006243 chemical reaction Methods 0.000 description 30
- 229910052799 carbon Inorganic materials 0.000 description 29
- 125000004104 aryloxy group Chemical group 0.000 description 28
- 239000000460 chlorine Substances 0.000 description 28
- 125000005346 substituted cycloalkyl group Chemical group 0.000 description 28
- 239000002904 solvent Substances 0.000 description 27
- 150000002500 ions Chemical class 0.000 description 26
- 239000010410 layer Substances 0.000 description 26
- 239000004743 Polypropylene Substances 0.000 description 25
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 24
- 125000000538 pentafluorophenyl group Chemical group FC1=C(F)C(F)=C(*)C(F)=C1F 0.000 description 23
- 238000012360 testing method Methods 0.000 description 23
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 22
- 238000004519 manufacturing process Methods 0.000 description 22
- 238000009826 distribution Methods 0.000 description 21
- 150000002431 hydrogen Chemical class 0.000 description 21
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 20
- 238000004458 analytical method Methods 0.000 description 20
- 229910052736 halogen Inorganic materials 0.000 description 20
- 150000002367 halogens Chemical class 0.000 description 20
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 description 19
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 18
- 125000000707 boryl group Chemical group B* 0.000 description 18
- 239000012071 phase Substances 0.000 description 18
- 239000002243 precursor Substances 0.000 description 18
- 238000007789 sealing Methods 0.000 description 18
- 125000004429 atom Chemical group 0.000 description 17
- 230000003197 catalytic effect Effects 0.000 description 17
- 229920001519 homopolymer Polymers 0.000 description 17
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 17
- 239000003153 chemical reaction reagent Substances 0.000 description 16
- 229910052735 hafnium Inorganic materials 0.000 description 16
- 239000012528 membrane Substances 0.000 description 16
- 239000012530 fluid Substances 0.000 description 15
- 229920000098 polyolefin Polymers 0.000 description 15
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 14
- 230000006870 function Effects 0.000 description 14
- 238000010438 heat treatment Methods 0.000 description 14
- 239000007787 solid Substances 0.000 description 14
- 229910052726 zirconium Inorganic materials 0.000 description 14
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 13
- LIKMAJRDDDTEIG-UHFFFAOYSA-N n-hexene Natural products CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 12
- 239000002879 Lewis base Substances 0.000 description 12
- 239000004327 boric acid Substances 0.000 description 12
- 230000008859 change Effects 0.000 description 12
- 229910052801 chlorine Inorganic materials 0.000 description 12
- 238000001816 cooling Methods 0.000 description 12
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 12
- 230000010354 integration Effects 0.000 description 12
- 150000007527 lewis bases Chemical class 0.000 description 12
- 229910052760 oxygen Inorganic materials 0.000 description 12
- 229920005653 propylene-ethylene copolymer Polymers 0.000 description 12
- 238000001228 spectrum Methods 0.000 description 12
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 12
- 150000001412 amines Chemical class 0.000 description 11
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 11
- 150000001721 carbon Chemical group 0.000 description 11
- 230000000052 comparative effect Effects 0.000 description 11
- 239000007789 gas Substances 0.000 description 11
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 11
- 238000003780 insertion Methods 0.000 description 11
- 230000037431 insertion Effects 0.000 description 11
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 11
- 229920005989 resin Polymers 0.000 description 11
- 239000011347 resin Substances 0.000 description 11
- 238000005481 NMR spectroscopy Methods 0.000 description 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 10
- 230000004087 circulation Effects 0.000 description 10
- 238000002425 crystallisation Methods 0.000 description 10
- 230000008025 crystallization Effects 0.000 description 10
- 230000007935 neutral effect Effects 0.000 description 10
- 229910052757 nitrogen Inorganic materials 0.000 description 10
- 239000001301 oxygen Substances 0.000 description 10
- 239000004698 Polyethylene Substances 0.000 description 9
- 229910052782 aluminium Inorganic materials 0.000 description 9
- 239000002585 base Substances 0.000 description 9
- 229910052796 boron Inorganic materials 0.000 description 9
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 9
- 125000004122 cyclic group Chemical group 0.000 description 9
- 238000005259 measurement Methods 0.000 description 9
- 230000003287 optical effect Effects 0.000 description 9
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 9
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 8
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 8
- 150000001450 anions Chemical class 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 8
- 238000001460 carbon-13 nuclear magnetic resonance spectrum Methods 0.000 description 8
- 239000011248 coating agent Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- 239000006260 foam Substances 0.000 description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 8
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 7
- 239000012190 activator Substances 0.000 description 7
- 229910000085 borane Inorganic materials 0.000 description 7
- 125000004432 carbon atom Chemical group C* 0.000 description 7
- 238000001035 drying Methods 0.000 description 7
- 125000005842 heteroatom Chemical group 0.000 description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 7
- 239000012968 metallocene catalyst Substances 0.000 description 7
- 238000002156 mixing Methods 0.000 description 7
- 229920000573 polyethylene Polymers 0.000 description 7
- 229920006395 saturated elastomer Polymers 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 7
- UORVGPXVDQYIDP-UHFFFAOYSA-N trihydridoboron Substances B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 description 7
- 238000005160 1H NMR spectroscopy Methods 0.000 description 6
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 6
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 6
- 239000004721 Polyphenylene oxide Substances 0.000 description 6
- 230000003213 activating effect Effects 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 238000007334 copolymerization reaction Methods 0.000 description 6
- 238000010828 elution Methods 0.000 description 6
- 229930195733 hydrocarbon Natural products 0.000 description 6
- 150000002430 hydrocarbons Chemical group 0.000 description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
- 150000002466 imines Chemical class 0.000 description 6
- 238000010606 normalization Methods 0.000 description 6
- 229910052698 phosphorus Inorganic materials 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 229920006300 shrink film Polymers 0.000 description 6
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 6
- 239000004215 Carbon black (E152) Substances 0.000 description 5
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 5
- 239000004709 Chlorinated polyethylene Substances 0.000 description 5
- 229920000089 Cyclic olefin copolymer Polymers 0.000 description 5
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 5
- 239000004793 Polystyrene Substances 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 230000004913 activation Effects 0.000 description 5
- 150000001336 alkenes Chemical class 0.000 description 5
- 239000004411 aluminium Substances 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 239000002249 anxiolytic agent Substances 0.000 description 5
- 229910002091 carbon monoxide Inorganic materials 0.000 description 5
- 239000008393 encapsulating agent Substances 0.000 description 5
- 235000013305 food Nutrition 0.000 description 5
- 125000005843 halogen group Chemical group 0.000 description 5
- 125000000623 heterocyclic group Chemical group 0.000 description 5
- 230000000977 initiatory effect Effects 0.000 description 5
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
- 239000011574 phosphorus Substances 0.000 description 5
- 229920000747 poly(lactic acid) Polymers 0.000 description 5
- 229920002223 polystyrene Polymers 0.000 description 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 5
- 238000012545 processing Methods 0.000 description 5
- 239000002516 radical scavenger Substances 0.000 description 5
- 239000010936 titanium Substances 0.000 description 5
- JLTRXTDYQLMHGR-UHFFFAOYSA-N trimethylaluminium Chemical compound C[Al](C)C JLTRXTDYQLMHGR-UHFFFAOYSA-N 0.000 description 5
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 4
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N 1-Heptene Chemical compound CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 4
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 4
- 239000002841 Lewis acid Substances 0.000 description 4
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 150000001639 boron compounds Chemical class 0.000 description 4
- 230000008602 contraction Effects 0.000 description 4
- 230000001276 controlling effect Effects 0.000 description 4
- 229920001971 elastomer Polymers 0.000 description 4
- 239000000806 elastomer Substances 0.000 description 4
- 125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- 150000007517 lewis acids Chemical class 0.000 description 4
- HZVOZRGWRWCICA-UHFFFAOYSA-N methanediyl Chemical group [CH2] HZVOZRGWRWCICA-UHFFFAOYSA-N 0.000 description 4
- CPOFMOWDMVWCLF-UHFFFAOYSA-N methyl(oxo)alumane Chemical class C[Al]=O CPOFMOWDMVWCLF-UHFFFAOYSA-N 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
- YPJKMVATUPSWOH-UHFFFAOYSA-N nitrooxidanyl Chemical compound [O][N+]([O-])=O YPJKMVATUPSWOH-UHFFFAOYSA-N 0.000 description 4
- 230000001590 oxidative effect Effects 0.000 description 4
- 238000012856 packing Methods 0.000 description 4
- 229920005604 random copolymer Polymers 0.000 description 4
- 239000000376 reactant Substances 0.000 description 4
- 239000002002 slurry Substances 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- 230000003595 spectral effect Effects 0.000 description 4
- 229920001897 terpolymer Polymers 0.000 description 4
- 239000004416 thermosoftening plastic Substances 0.000 description 4
- 150000003568 thioethers Chemical class 0.000 description 4
- 229910052720 vanadium Inorganic materials 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- 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 3
- UQRONKZLYKUEMO-UHFFFAOYSA-N 4-methyl-1-(2,4,6-trimethylphenyl)pent-4-en-2-one Chemical group CC(=C)CC(=O)Cc1c(C)cc(C)cc1C UQRONKZLYKUEMO-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 239000007848 Bronsted acid Substances 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 3
- COOXAWDWHWRVRD-UHFFFAOYSA-N C[Ti]C Chemical compound C[Ti]C COOXAWDWHWRVRD-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- CMEWLCATCRTSGF-UHFFFAOYSA-N N,N-dimethyl-4-nitrosoaniline Chemical compound CN(C)C1=CC=C(N=O)C=C1 CMEWLCATCRTSGF-UHFFFAOYSA-N 0.000 description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 125000000129 anionic group Chemical group 0.000 description 3
- 125000005428 anthryl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C(*)=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 description 3
- 239000012298 atmosphere Substances 0.000 description 3
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- 238000007664 blowing Methods 0.000 description 3
- 229910052794 bromium Inorganic materials 0.000 description 3
- 238000006758 bulk electrolysis reaction Methods 0.000 description 3
- 150000001768 cations Chemical class 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 125000003963 dichloro group Chemical group Cl* 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical class [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 description 3
- 238000005194 fractionation Methods 0.000 description 3
- 125000000524 functional group Chemical group 0.000 description 3
- 238000005227 gel permeation chromatography Methods 0.000 description 3
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- 229910052738 indium Inorganic materials 0.000 description 3
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 3
- 238000009413 insulation Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- DLEDOFVPSDKWEF-UHFFFAOYSA-N lithium butane Chemical compound [Li+].CCC[CH2-] DLEDOFVPSDKWEF-UHFFFAOYSA-N 0.000 description 3
- 238000011068 loading method Methods 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- MZRVEZGGRBJDDB-UHFFFAOYSA-N n-Butyllithium Substances [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 3
- 125000001624 naphthyl group Chemical group 0.000 description 3
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 3
- 239000007800 oxidant agent Substances 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- 230000000379 polymerizing effect Effects 0.000 description 3
- 229920000915 polyvinyl chloride Polymers 0.000 description 3
- 238000001556 precipitation Methods 0.000 description 3
- 238000010926 purge Methods 0.000 description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 238000007670 refining Methods 0.000 description 3
- 229910052711 selenium Inorganic materials 0.000 description 3
- 239000011669 selenium Substances 0.000 description 3
- 229920006126 semicrystalline polymer Polymers 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- 229960001866 silicon dioxide Drugs 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 229920006029 tetra-polymer Polymers 0.000 description 3
- 238000003856 thermoforming Methods 0.000 description 3
- 229910052719 titanium Inorganic materials 0.000 description 3
- 230000009466 transformation Effects 0.000 description 3
- 230000007704 transition Effects 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- PZWQOGNTADJZGH-SNAWJCMRSA-N (2e)-2-methylpenta-2,4-dienoic acid Chemical compound OC(=O)C(/C)=C/C=C PZWQOGNTADJZGH-SNAWJCMRSA-N 0.000 description 2
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical compound C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 description 2
- 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 2
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Cited By (4)
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Families Citing this family (346)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1522553B1 (en) | 1998-07-01 | 2007-04-11 | ExxonMobil Chemical Patents Inc. | Elastic blends comprising crystalline polymer and crystallizable polymers of propylene |
US6727361B2 (en) | 2000-11-07 | 2004-04-27 | Symyx Technologies, Inc. | Phosphino substituted pyridine amine ligands |
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US20050032959A1 (en) * | 2003-05-05 | 2005-02-10 | Cheung Yunwa Wilson | Filled thermoplastic olefin composition |
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US7671106B2 (en) | 2004-03-17 | 2010-03-02 | Dow Global Technologies Inc. | Cap liners, closures and gaskets from multi-block polymers |
EP2357203B1 (en) * | 2004-03-17 | 2017-05-24 | Dow Global Technologies LLC | Catalyst composition comprising shuttling agent for higher olefin multi-block copolymer formation |
TWI391412B (zh) * | 2004-03-17 | 2013-04-01 | Dow Global Technologies Llc | 包含用於形成乙烯多嵌段共聚物之穿梭劑的催化劑組成物 |
US7687442B2 (en) * | 2004-03-17 | 2010-03-30 | Dow Global Technologies Inc. | Low molecular weight ethylene/α-olefin interpolymer as base lubricant oils |
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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 |
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 |
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 |
JP4562169B2 (ja) * | 2004-04-12 | 2010-10-13 | 株式会社高純度化学研究所 | Hf系酸化物ゲート絶縁膜のプリカーサーの精製方法 |
US7645829B2 (en) | 2004-04-15 | 2010-01-12 | Exxonmobil Chemical Patents Inc. | Plasticized functionalized propylene copolymer adhesive composition |
CA2563043C (en) | 2004-04-19 | 2013-04-02 | Shaun Parkinson | Composition suitable for single-sided, low-noise, stretch cling film and films made therefrom |
DE102004020525A1 (de) | 2004-04-26 | 2005-11-10 | Basell Polyolefine Gmbh | Katalysatorsystem zur Olefinpolymerisation, dessen Herstellung und Verwendung |
ITMI20040866A1 (it) * | 2004-04-30 | 2004-07-30 | Colines Srl | Procedimento ed apparto per la realizzazione di una lastra a bolle d'aria |
US20080033124A1 (en) * | 2004-06-21 | 2008-02-07 | Peijun Jiang | Polymerization Process |
DE602005019753D1 (de) * | 2004-08-31 | 2010-04-15 | Dow Global Technologies Inc | Für thermoformbare folien geeignete zusammensetzung und daraus hergestellte artikel |
US7256296B2 (en) | 2004-09-22 | 2007-08-14 | Symyx Technologies, Inc. | Heterocycle-amine ligands, compositions, complexes, and catalysts |
US7387980B2 (en) | 2004-09-22 | 2008-06-17 | Symyx Technologies, Inc. | Methods of using heterocycle-amine ligands, compositions, complexes, and catalysts |
JP2008516068A (ja) | 2004-10-13 | 2008-05-15 | エクソンモービル・ケミカル・パテンツ・インク | エラストマー性反応ブレンド組成物 |
US9227346B2 (en) | 2004-10-22 | 2016-01-05 | Dow Global Technologies Llc | Plastic composite articles and methods of making same |
US7829623B2 (en) | 2004-11-05 | 2010-11-09 | Exxonmobil Chemical Patents Inc. | Thermoplastic vulcanizates having improved fabricability |
US7745526B2 (en) | 2004-11-05 | 2010-06-29 | Exxonmobil Chemical Patents Inc. | Transparent polyolefin compositions |
JP4860483B2 (ja) | 2004-11-26 | 2012-01-25 | 三井化学株式会社 | ポリプロピレンの不織布およびその用途 |
US7705157B2 (en) | 2004-12-16 | 2010-04-27 | Symyx Solutions, Inc. | Phenol-heterocyclic ligands, metal complexes, and their uses as catalysts |
EP1828303B1 (en) | 2004-12-17 | 2009-08-26 | ExxonMobil Chemical Patents, Inc., A Corporation of the State of Delaware | Heterogeneous polymer blends and molded articles therefrom |
CA2586907C (en) | 2004-12-17 | 2010-03-16 | Exxonmobil Chemical Patents Inc. | Polymer blends and nonwoven articles therefrom |
EP1831304B1 (en) | 2004-12-17 | 2010-05-12 | ExxonMobil Chemical Patents Inc. | Homogeneous polymer blend and articles therefrom |
ES2328611T3 (es) | 2004-12-17 | 2009-11-16 | Exxonmobil Chemical Patents Inc. | Peliculas de mezclas de polimeros. |
AU2005319179B2 (en) * | 2004-12-21 | 2011-10-13 | Dow Global Technologies Llc | Polypropylene-based adhesive compositions |
GB2423994B (en) * | 2005-03-04 | 2008-07-30 | Bespak Plc | Seal for a dispensing apparatus |
MX2007011331A (es) * | 2005-03-17 | 2007-10-02 | Dow Global Technologies Inc | Mezclas de polimeros a partir de interpolimeros de etileno/alfa-olefinas y articulos moldeados flexibles hechos a partir de los mismos. |
TW200643084A (en) * | 2005-03-17 | 2006-12-16 | Dow Global Technologies Inc | Impact modification of thermoplastics with ethylene/α-olefin interpolymers |
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 |
US7786216B2 (en) * | 2005-03-17 | 2010-08-31 | Dow Global Technologies Inc. | Oil based blends of interpolymers of ethylene/α-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 |
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 |
RU2007134418A (ru) * | 2005-03-17 | 2009-03-20 | Дау Глобал Текнолоджиз Инк. (Us) | ВОЛОКНА, ПОЛУЧАЕМЫЕ ИЗ СОПОЛИМЕРОВ ЭТИЛЕНА/α-ОЛЕФИНОВ |
BR122017012540B1 (pt) | 2005-03-17 | 2022-09-27 | Dow Global Technologies Inc | Mistura polimérica, perfil e gaxeta |
KR101243003B1 (ko) * | 2005-03-17 | 2013-03-12 | 다우 글로벌 테크놀로지스 엘엘씨 | 에틸렌/α-올레핀의 혼성중합체의 유변성 개질 및 그로부터제조한 성형품 |
BRPI0609824B1 (pt) * | 2005-03-17 | 2022-09-27 | Dow Global Technologies Inc | Composição de mistura polimérica e gaxeta |
CA2601273A1 (en) * | 2005-03-17 | 2006-09-28 | Dow Global Technologies Inc. | Adhesive and marking compositions made from interpolymers of ethylene/alpha-olefins |
RU2007134341A (ru) * | 2005-03-17 | 2009-03-20 | Дау Глобал Текнолоджиз Инк. (Us) | КОМПОЗИЦИИ ИЗ ПОЛИБЛОЧНОГО ИНТЕРПОЛИМЕРА ЭТИЛЕНА/α-ОЛЕФИНА ДЛЯ ЭЛАСТИЧНЫХ ПЛЕНОК И ЛАМИНАТОВ |
RU2007134421A (ru) * | 2005-03-17 | 2009-03-20 | Дау Глобал Текнолоджиз Инк. (Us) | КОМПОЗИЦИИ ПОЛИБЛОЧНОГО ИНТЕРПОЛИМЕРА ЭТИЛЕНА/α-ОЛЕФИНА ДЛЯ ПОЛУЧЕННЫХ ЭКСТРУЗИЕЙ С РАЗДУВОМ ПЛЕНОК С ВЫСОКОЙ ЛИПКОСТЬЮ ПРИ НАГРЕВАНИИ |
US8084537B2 (en) * | 2005-03-17 | 2011-12-27 | Dow Global Technologies Llc | Polymer blends from interpolymers of ethylene/α-olefin with improved compatibility |
TWI375685B (en) * | 2005-03-17 | 2012-11-01 | Dow Global Technologies Llc | Compositions of ethylene/alpha-olefin multi-block interpolymer suitable for films |
US7585917B2 (en) | 2005-06-13 | 2009-09-08 | Exxonmobil Chemical Patents Inc. | Thermoplastic blend compositions |
EP1891123B1 (en) * | 2005-06-13 | 2018-08-29 | Basell Polyolefine GmbH | Process for the copolymerization of propylene |
CN101248133B (zh) | 2005-06-24 | 2012-11-21 | 埃克森美孚化学专利公司 | 官能化丙烯共聚物粘合剂组合物 |
ES2490990T3 (es) | 2005-07-11 | 2014-09-04 | Dow Global Technologies Llc | Composiciones que comprenden polímeros de olefina injertados con silano |
DE102005035477A1 (de) | 2005-07-26 | 2007-02-01 | Basell Polyolefine Gmbh | Verfahren zur Steuerung der relativen Aktivität der unterschiedlichen aktiven Zentren von Hybridkatalysatoren |
RU2415206C2 (ru) * | 2005-08-19 | 2011-03-27 | Дау Глобал Текнолоджиз, Инк. | Слои из нетканого материала, изготовленного раздувом расплава полимера на основе пропилена, и композитные структуры |
JP5411502B2 (ja) * | 2005-09-15 | 2014-02-12 | ダウ グローバル テクノロジーズ エルエルシー | 重合性シャトリング剤による接触オレフィンブロック共重合体 |
AR058448A1 (es) * | 2005-09-15 | 2008-02-06 | Dow Global Technologies Inc | Control de arquitectura del polimero y distribucoin de peso molecular va el agente de transferencia multi- centrado |
US8119748B2 (en) * | 2005-09-28 | 2012-02-21 | Dow Global Technologies Llc | High activity, low molecular weight olefin polymerization process |
TWI386310B (zh) * | 2005-10-07 | 2013-02-21 | Dow Global Technologies Llc | 多層彈性膜結構物 |
RU2426650C2 (ru) * | 2005-10-26 | 2011-08-20 | Дау Глобал Текнолоджиз Инк. | Многослойные предварительно вытянутые эластичные изделия |
EP1951511B1 (en) * | 2005-10-26 | 2018-09-12 | Dow Global Technologies LLC | Multi-layer, elastic articles |
EP1943308B1 (en) | 2005-10-31 | 2010-06-23 | Dow Global Technologies Inc. | Propylene-based elastomeric composition |
US8153243B2 (en) | 2005-12-09 | 2012-04-10 | Dow Global Technologies Llc | Interpolymers suitable for multilayer films |
AR058852A1 (es) | 2005-12-09 | 2008-02-27 | Dow Global Technologies Inc | Procesos para controlar la distribucion del peso molecular en las composiciones de etileno/alfa olefina |
US8927108B2 (en) * | 2006-01-10 | 2015-01-06 | Exxonmobil Chemical Patents Inc. | Films incorporating polymeric material combinations, articles made therefrom, and methods of making such films and articles |
WO2007084219A1 (en) | 2006-01-17 | 2007-07-26 | Exxonmobil Chemical Patents Inc. | Process for making dynamically-loaded articles comprising propylene-based elastomers, composition for use in such processes, and article made using such processes |
WO2007124303A2 (en) | 2006-04-19 | 2007-11-01 | Dow Global Technologies, Inc. | Method for blending materials in an extruder, the manufactured article and material pre-mix |
RU2008147910A (ru) * | 2006-05-05 | 2010-06-10 | Дау Глобал Текнолоджиз Инк. (Us) | Орто-металлированные гафнивые комплексы имидазольных лиганов |
GB0611331D0 (en) | 2006-06-09 | 2006-07-19 | Exxonmobil Chem Patents Inc | Transparent coextruded films and processes for making such films |
US8617717B2 (en) * | 2006-06-09 | 2013-12-31 | Exxonmobil Chemical Patents Inc. | Heat sealable films from propylene and α-olefin units |
CN103121320B (zh) | 2006-06-14 | 2015-06-24 | 艾利丹尼森公司 | 可顺应和可冲切的轴向定向的标签原料和标签及制备方法 |
EP2363445A1 (en) | 2006-06-15 | 2011-09-07 | Dow Global Technologies LLC | Functionalized propylene interpolymers, compositions and articles prepared therefrom, and methods for making the same |
CN101484315B (zh) | 2006-06-20 | 2013-04-10 | 艾利丹尼森公司 | 用于热熔粘合剂标记和标签原料以及此种标签的多层聚合膜 |
ATE501185T1 (de) * | 2006-06-27 | 2011-03-15 | Univation Tech Llc | Ethylen-alpha-olefin-copolymere und polymerisierungsverfahren für deren herstellung |
CN101516931B (zh) | 2006-06-27 | 2015-08-26 | 尤尼威蒂恩技术有限责任公司 | 用于滚塑和注塑制品的以茂金属催化剂制备的聚合物 |
KR101408618B1 (ko) * | 2006-06-27 | 2014-06-17 | 유니베이션 테크놀로지즈, 엘엘씨 | 메탈로센 촉매를 이용한 향상된 중합 방법, 이의 중합체 생성물 및 최종 용도 |
US7632907B2 (en) * | 2006-06-28 | 2009-12-15 | Chevron Phillips Chemical Company Lp | Polyethylene film having improved mechanical and barrier properties and method of making same |
EP2041221B1 (en) | 2006-06-29 | 2014-06-04 | Dow Global Technologies LLC | PROCESSES and kit FOR MAKING THERMOPLASTIC ARTICLES USING AN IMPROVED MASTERBATCH |
US8202467B2 (en) | 2006-08-02 | 2012-06-19 | Exxonmobil Chemical Patents Inc. | Propylene-based polymer article |
GB2441329B (en) * | 2006-09-04 | 2011-06-29 | Bespak Plc | Seal for a dispensing apparatus |
KR20090053848A (ko) * | 2006-09-06 | 2009-05-27 | 다우 글로벌 테크놀로지스 인크. | 올레핀 블럭 인터폴리머를 포함하는 편직물 |
US7847099B2 (en) | 2006-09-21 | 2010-12-07 | California Institute Of Technology | Non-metallocene organometallic complexes and related methods and systems |
US8124234B2 (en) * | 2006-11-01 | 2012-02-28 | Dow Global Technologies Llc | Polyurethane compositions and articles prepared therefrom, and methods for making the same |
JP5061842B2 (ja) * | 2006-11-01 | 2012-10-31 | 王子製紙株式会社 | 二軸延伸ポリプロピレンフィルム |
CN101589081A (zh) | 2006-11-30 | 2009-11-25 | 陶氏环球技术公司 | 具有抗皱性的弹力织物和衣物 |
JP2010511801A (ja) * | 2006-11-30 | 2010-04-15 | ダウ グローバル テクノロジーズ インコーポレイティド | 重重量の伸縮性布地のためのオレフィンブロック組成物 |
WO2008067545A2 (en) * | 2006-11-30 | 2008-06-05 | Dow Global Technologies Inc. | Fabric comprising elastic fibres of cross-linked ethylene polymer |
JP5341770B2 (ja) * | 2006-12-15 | 2013-11-13 | フイナ・テクノロジー・インコーポレーテツド | ポリプロピレンインフレーションフィルム |
US7713636B2 (en) * | 2006-12-15 | 2010-05-11 | Exxonmobil Chemical Patents Inc. | Multi-layer films comprising propylene-based polymers |
US8143352B2 (en) | 2006-12-20 | 2012-03-27 | Exxonmobil Research And Engineering Company | Process for fluid phase in-line blending of polymers |
US8242237B2 (en) | 2006-12-20 | 2012-08-14 | Exxonmobil Chemical Patents Inc. | Phase separator and monomer recycle for supercritical polymerization process |
EP2125918B1 (en) * | 2006-12-21 | 2012-06-27 | Dow Global Technologies LLC | Functionalized olefin polymers, compositions and articles prepared therefrom, and methods for making the same |
US8288470B2 (en) | 2006-12-21 | 2012-10-16 | Dow Global Technologies Llc | Polyolefin compositions and articles prepared therefrom, and methods for making the same |
JP5007116B2 (ja) * | 2006-12-27 | 2012-08-22 | 日本ポリプロ株式会社 | オレフィン共重合体の製造方法 |
US20100075079A1 (en) * | 2006-12-29 | 2010-03-25 | Dow Global Technologies Inc. | Ozone resistant compositions and articles |
CN101595253A (zh) * | 2007-01-16 | 2009-12-02 | 陶氏环球技术公司 | 烯烃嵌段组合物的不褪色织物和衣物 |
BRPI0806194A2 (pt) * | 2007-01-16 | 2011-08-30 | Dow Global Technologies Inc | fio tingido em cone |
TW200914267A (en) * | 2007-01-16 | 2009-04-01 | Dow Global Technologies Inc | Stretch fabrics and garments of olefin block polymers |
US7951732B2 (en) | 2007-01-26 | 2011-05-31 | Exxonmobil Chemical Patents Inc. | Elastomeric laminates for consumer products |
US8080610B2 (en) | 2007-03-06 | 2011-12-20 | Exxonmobil Research And Engineering Company | Monomer recycle process for fluid phase in-line blending of polymers |
WO2008109212A1 (en) * | 2007-03-06 | 2008-09-12 | Exxonmobil Chemical Patents Inc. | Polymer production under supersolution conditions |
EP2121776B1 (en) * | 2007-03-07 | 2012-12-12 | Dow Global Technologies LLC | Tethered supported transition metal complex |
US8241753B2 (en) | 2007-06-04 | 2012-08-14 | Exxonmobil Chemical Patents Inc. | Composite thermoplastic elastomer structures with high adhesion performance and uses for the same |
EP2167574A2 (en) * | 2007-07-09 | 2010-03-31 | Dow Global Technologies Inc. | Olefin block interpolymer composition suitable for fibers |
ES2506096T3 (es) | 2007-07-16 | 2014-10-13 | Dow Global Technologies Llc | Polímeros funcionalizados y artículos preparados a partir de los mismos |
US8653191B2 (en) * | 2007-07-27 | 2014-02-18 | Dow Global Technologies Llc | Polyolefin compositions and articles prepared therefrom, and methods for making the same |
PL2185599T3 (pl) | 2007-08-24 | 2019-07-31 | W.R. Grace & Co. - Conn | Samoograniczający system katalityczny o kontrolowanym stosunku glinu do SCA i sposób |
GB0717376D0 (en) | 2007-09-07 | 2007-10-17 | Exxonmobil Chem Patents Inc | Composition and manufacture thereof |
US7910637B2 (en) | 2007-09-13 | 2011-03-22 | Exxonmobil Research And Engineering Company | In-line blending of plasticizers with a base polymer |
CN101855249B (zh) | 2007-09-13 | 2013-02-13 | 埃克森美孚研究工程公司 | 在线生产增塑聚合物和增塑聚合物共混物的方法 |
EP2042552A1 (en) * | 2007-09-27 | 2009-04-01 | Borealis Technology Oy | Polyolefin compositions having improved optical and mechanical properties |
EP2203512A1 (en) * | 2007-09-28 | 2010-07-07 | Dow Global Technologies Inc. | Thermoplastic olefin composition with improved heat distortion temperature |
DE102007048090A1 (de) * | 2007-10-05 | 2009-04-09 | Wipak Walothen Gmbh | Kuvertfenster |
JP5588872B2 (ja) | 2007-10-22 | 2014-09-10 | スティロン ヨーロッパ ゲゼルシャフト ミット ベシュレンクテル ハフツング | 物品を成形するためのポリマー組成物及び方法 |
EP2052857A1 (en) | 2007-10-22 | 2009-04-29 | Dow Global Technologies Inc. | Multilayer films |
US8609772B2 (en) | 2007-10-23 | 2013-12-17 | Exxonmobil Chemical Patents Inc. | Elastic films having improved mechanical and elastic properties and methods for making the same |
JP5580208B2 (ja) * | 2007-11-27 | 2014-08-27 | ダウ グローバル テクノロジーズ エルエルシー | 容器製造用多層構造体及びその包装 |
US7910679B2 (en) | 2007-12-20 | 2011-03-22 | Exxonmobil Research And Engineering Company | Bulk homogeneous polymerization process for ethylene propylene copolymers |
CN103254497B (zh) | 2007-12-20 | 2015-11-18 | 埃克森美孚研究工程公司 | 生产聚丙烯和乙烯-丙烯共聚物的共混物的在线共混方法 |
WO2009082463A1 (en) | 2007-12-20 | 2009-07-02 | Exxonmobil Research And Engineering Company | In-line process to produce pellet-stable polyolefins |
EP2080615A1 (en) * | 2008-01-18 | 2009-07-22 | Dow Global Technologies Inc. | Coated substrates and packages prepared therefrom |
US8088163B1 (en) | 2008-02-06 | 2012-01-03 | Kleiner Jeffrey B | Tools and methods for spinal fusion |
US7858817B2 (en) | 2008-03-10 | 2010-12-28 | Exxonmobil Chemical Patents Inc. | Metallocene-substituted pyridyl amines, their metal complexes, and processes for production and use thereof |
WO2009114761A2 (en) | 2008-03-14 | 2009-09-17 | Dow Global Technologies Inc. | Improved process for shaping polymeric articles |
US8067512B2 (en) | 2008-04-10 | 2011-11-29 | Exxonmobil Research And Engineering Company | Monomer/solvent separation and recycle process for propylene containing polymers |
US8398833B2 (en) * | 2008-04-21 | 2013-03-19 | Honeywell International Inc. | Use of DC magnetron sputtering systems |
US20090269566A1 (en) * | 2008-04-23 | 2009-10-29 | Berry Plastics Corporation | Pre-stretched multi-layer stretch film |
US7939610B2 (en) | 2008-05-22 | 2011-05-10 | Exxonmobil Research And Engineering Company | Polymerization processes for broadened molecular weight distribution |
US7867433B2 (en) | 2008-05-30 | 2011-01-11 | Exxonmobil Chemical Patents Inc. | Polyolefin-based crosslinked articles |
US8765832B2 (en) | 2011-10-14 | 2014-07-01 | Exxonmobil Chemical Patents Inc. | Polyolefin-based crosslinked compositions and methods of making them |
US8858986B2 (en) | 2008-06-12 | 2014-10-14 | 3M Innovative Properties Company | Biocompatible hydrophilic compositions |
US8283428B2 (en) | 2008-06-20 | 2012-10-09 | Exxonmobil Chemical Patents Inc. | Polymacromonomer and process for production thereof |
US8802797B2 (en) | 2008-06-20 | 2014-08-12 | Exxonmobil Chemical Patents Inc. | Vinyl-terminated macromonomer oligomerization |
WO2009158100A2 (en) | 2008-06-27 | 2009-12-30 | Exxonmobil Chemical Patents Inc. | High shrinkage propylene-based films |
US8796383B2 (en) * | 2008-06-30 | 2014-08-05 | Fina Technology, Inc. | Polypropylene and polylactic acid formulations for heat seal applications |
US8710163B2 (en) | 2008-07-25 | 2014-04-29 | Exxonmobil Chemical Patents Inc. | Pyridyldiamido transition metal complexes, production and use thereof |
US8674040B2 (en) * | 2008-07-25 | 2014-03-18 | Exxonmobil Chemical Patents Inc. | Pyridyldiamido transition metal complexes, production and use thereof |
US7973116B2 (en) * | 2008-07-25 | 2011-07-05 | Exxonmobil Chemical Patents Inc. | Pyridyldiamido transition metal complexes, production and use thereof |
US8394902B2 (en) | 2008-07-25 | 2013-03-12 | Exxonmobil Chemical Patents Inc. | Pyridyldiamido transition metal complexes, production and use thereof |
US8580902B2 (en) | 2008-08-01 | 2013-11-12 | Exxonmobil Chemical Patents Inc. | Catalyst system, process for olefin polymerization, and polymer compositions produced therefrom |
WO2010014344A2 (en) | 2008-08-01 | 2010-02-04 | Exxonmobil Chemical Patents Inc. | Catalyst system and process for olefin polymerization |
US20120015854A1 (en) | 2008-08-08 | 2012-01-19 | Ravishankar Periagaram S | Olefinic Copolymer Compositions for Viscosity Modification of Motor Oil |
JP5628809B2 (ja) * | 2008-08-21 | 2014-11-19 | ダウ グローバル テクノロジーズ エルエルシー | 混合された選択性制御剤を含む触媒組成物及び該触媒組成物を使用する重合方法 |
US8399586B2 (en) | 2008-09-05 | 2013-03-19 | Exxonmobil Research And Engineering Company | Process for feeding ethylene to polymerization reactors |
JP2012503682A (ja) * | 2008-09-23 | 2012-02-09 | ダウ グローバル テクノロジーズ エルエルシー | 分子量の変化が低減されたラジカル官能化オレフィン系ポリマーおよび方法 |
US9168718B2 (en) | 2009-04-21 | 2015-10-27 | Exxonmobil Chemical Patents Inc. | Method for producing temperature resistant nonwovens |
US10161063B2 (en) | 2008-09-30 | 2018-12-25 | Exxonmobil Chemical Patents Inc. | Polyolefin-based elastic meltblown fabrics |
US9498932B2 (en) | 2008-09-30 | 2016-11-22 | Exxonmobil Chemical Patents Inc. | Multi-layered meltblown composite and methods for making same |
RU2011116768A (ru) * | 2008-10-03 | 2013-03-20 | ДАУ ГЛОБАЛ ТЕКНОЛОДЖИЗ ЭлЭлСи | Композиции для износостойких пен и способы для их производства |
USD853560S1 (en) | 2008-10-09 | 2019-07-09 | Nuvasive, Inc. | Spinal implant insertion device |
US20100119855A1 (en) * | 2008-11-10 | 2010-05-13 | Trazollah Ouhadi | Thermoplastic Elastomer with Excellent Adhesion to EPDM Thermoset Rubber and Low Coefficient of Friction |
US20100120953A1 (en) * | 2008-11-12 | 2010-05-13 | Aarts Maarten W | Highly Filled, Propylene-Ethylene Copolymer Compositions |
US20100125124A1 (en) * | 2008-11-17 | 2010-05-20 | Fina Technology, Inc. | Methods of catalyst activation |
US9717403B2 (en) | 2008-12-05 | 2017-08-01 | Jeffrey B. Kleiner | Method and apparatus for performing retro peritoneal dissection |
US8366748B2 (en) * | 2008-12-05 | 2013-02-05 | Kleiner Jeffrey | Apparatus and method of spinal implant and fusion |
US8106127B2 (en) | 2008-12-15 | 2012-01-31 | Exxonmobil Chemical Patents Inc. | Heterogeneous in-reactor polymer blends |
US8101685B2 (en) | 2008-12-15 | 2012-01-24 | Exxonmobil Chemical Patents Inc. | Thermoplastic elastomer polyolefin in-reactor blends and molded articles therefrom |
US8227547B2 (en) | 2008-12-15 | 2012-07-24 | Exxonmobil Chemical Patents Inc. | Foamable thermoplastic reactor blends and foam article therefrom |
US8410217B2 (en) | 2008-12-15 | 2013-04-02 | Exxonmobil Chemical Patents Inc. | Thermoplastic polyolefin blends |
US8497325B2 (en) | 2008-12-15 | 2013-07-30 | Exxonmobil Chemical Patents Inc. | Thermoplastic polyolefin blends and films therefrom |
US8093335B2 (en) | 2008-12-15 | 2012-01-10 | Exxonmobil Chemical Patents Inc. | Thermoplastic polyolefin in-reactor blends and molded articles therefrom |
US8529821B2 (en) | 2009-01-30 | 2013-09-10 | Dow Global Technologies Llc | Polymeric compositions and filled TPO articles having improved aesthetics |
USD656610S1 (en) | 2009-02-06 | 2012-03-27 | Kleiner Jeffrey B | Spinal distraction instrument |
EP2401147B1 (en) | 2009-02-27 | 2015-06-24 | ExxonMobil Chemical Patents Inc. | Biaxially elastic nonwoven laminates having inelastic zones |
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 |
CN102439210B (zh) | 2009-03-31 | 2015-12-16 | 3M创新有限公司 | 尺寸上稳定的非织造纤维幅材及其制造和使用方法 |
DE202009018172U1 (de) * | 2009-04-22 | 2011-04-07 | Hottinger Baldwin Messtechnik Gmbh | Optische Dehnungsmessvorrichtung |
US8378042B2 (en) | 2009-04-28 | 2013-02-19 | Exxonmobil Chemical Patents Inc. | Finishing process for amorphous polymers |
US20120028865A1 (en) | 2010-07-28 | 2012-02-02 | Sudhin Datta | Viscosity Modifiers Comprising Blends of Ethylene-Based Copolymers |
BRPI1007705A2 (pt) * | 2009-05-08 | 2019-09-24 | Dow Global Technologies Llc | película retrátil orientada em multicamada e envoltório retrátil |
US9017593B2 (en) | 2009-06-16 | 2015-04-28 | Exxonmobil Chemical Patents Inc. | Composite materials comprising propylene-based polymer blend coatings |
EP2275254A1 (en) | 2009-07-17 | 2011-01-19 | Dow Global Technologies Inc. | Coated substrates and packages prepared therefrom |
WO2011011124A1 (en) | 2009-07-23 | 2011-01-27 | Exxonmobil Chemical Patents Inc. | Polypropylene-based elastomer coating compositions |
US8975334B2 (en) | 2009-07-23 | 2015-03-10 | Exxonmobil Chemical Patents Inc. | Crosslinkable propylene-based copolymers, methods for preparing the same, and articles made therefrom |
US9005739B2 (en) | 2009-07-23 | 2015-04-14 | Exxonmobil Chemical Patents Inc. | Laminated articles and their production |
US8394892B2 (en) * | 2009-09-14 | 2013-03-12 | Sumitomo Chemical Company, Ltd. | High performance thermoplastic elastomer composition |
US9173694B2 (en) | 2009-09-18 | 2015-11-03 | Spinal Surgical Strategies, Llc | Fusion cage with combined biological delivery system |
US8685031B2 (en) | 2009-09-18 | 2014-04-01 | Spinal Surgical Strategies, Llc | Bone graft delivery system |
USD723682S1 (en) | 2013-05-03 | 2015-03-03 | Spinal Surgical Strategies, Llc | Bone graft delivery tool |
US9186193B2 (en) | 2009-09-18 | 2015-11-17 | Spinal Surgical Strategies, Llc | Fusion cage with combined biological delivery system |
US9629729B2 (en) | 2009-09-18 | 2017-04-25 | Spinal Surgical Strategies, Llc | Biological delivery system with adaptable fusion cage interface |
US9879160B2 (en) | 2009-10-29 | 2018-01-30 | Exxonmobil Chemical Patents Inc. | Pressure-sensitive hot melt adhesive compositions |
JP5606725B2 (ja) * | 2009-11-27 | 2014-10-15 | 日東電工株式会社 | 塗膜保護シート |
JP5748952B2 (ja) * | 2009-11-27 | 2015-07-15 | 日東電工株式会社 | 塗膜保護シート |
EP2329947A1 (en) | 2009-12-03 | 2011-06-08 | ExxonMobil Oil Corporation | Multi-layer opaque films, methods of manufacture and use thereof |
WO2011075619A1 (en) | 2009-12-17 | 2011-06-23 | 3M Innovative Properties Company | Dimensionally stable nonwoven fibrous webs, melt blown fine fibers, and methods of making and using the same |
AU2010339869B2 (en) | 2009-12-17 | 2014-12-18 | 3M Innovative Properties Company | Dimensionally stable nonwoven fibrous webs and methods of making and using the same |
ES2665762T3 (es) | 2009-12-18 | 2018-04-27 | Dow Global Technologies Llc | Películas y artículos preparados a partir de las mismas |
BR112012015365A2 (pt) | 2009-12-23 | 2020-09-15 | Invista Technologies S.A.R.L. | artigo e método para preparar um pano |
CN107411883A (zh) | 2009-12-23 | 2017-12-01 | 英威达技术有限公司 | 包括聚烯烃弹性纤维的弹力制品 |
KR20120114314A (ko) | 2009-12-23 | 2012-10-16 | 인비스타 테크놀러지스 에스.에이.알.엘. | 점착 방지 첨가제를 함유하는 탄성 섬유 |
MX2012007399A (es) | 2009-12-23 | 2012-07-17 | Invista Tech Sarl | Fibra elastica de poliolefina. |
US9416206B2 (en) | 2010-01-22 | 2016-08-16 | Exxonmobil Chemical Patents Inc. | Lubricating oil compositions and method for making them |
AU2011218854B2 (en) | 2010-02-23 | 2015-03-12 | 3M Innovative Properties Company | Dimensionally stable nonwoven fibrous webs and methods of making and using the same |
US20110218283A1 (en) * | 2010-03-02 | 2011-09-08 | Nadeem Akhtar Bokhari | Reactor thermoplastic polyolefin elastomer composition |
BR112012022568A2 (pt) | 2010-03-12 | 2016-08-30 | Exxonmobil Chem Patents Inc | método para produzir não tecidos resistentes a temperatura |
US8278403B2 (en) * | 2010-07-08 | 2012-10-02 | Fina Technology, Inc. | Multi-component catalyst systems and polymerization processes for forming broad composition distribution polymers |
TW201221714A (en) | 2010-10-14 | 2012-06-01 | 3M Innovative Properties Co | Dimensionally stable nonwoven fibrous webs and methods of making and using the same |
US9109143B2 (en) | 2010-10-15 | 2015-08-18 | Exxonmobil Chemical Patents Inc. | Polypropylene-based adhesive compositions |
US8980415B2 (en) | 2010-12-03 | 2015-03-17 | Benoit Ambroise | Antistatic films and methods to manufacture the same |
BRPI1107080A2 (pt) | 2010-12-30 | 2013-04-24 | Braskem Sa | artigo formando por sopro e compressço |
WO2012106025A1 (en) | 2011-01-31 | 2012-08-09 | Exxonmobil Chemical Patents Inc. | Coextruded films and processes for making such films |
EP2675844B1 (en) | 2011-02-15 | 2017-10-11 | ExxonMobil Chemical Patents Inc. | Thermoplastic polyolefin blends |
US8470922B2 (en) | 2011-03-03 | 2013-06-25 | Exxonmobil Chemical Patents Inc. | Ethylene-vinyl alcohol based thermoplastic elastomers and vulcanizates |
US8455597B2 (en) | 2011-03-25 | 2013-06-04 | Exxonmobil Chemical Patents Inc. | Catalysts and methods of use thereof to produce vinyl terminated polymers |
US8501894B2 (en) | 2011-03-25 | 2013-08-06 | Exxonmobil Chemical Patents Inc. | Hydrosilyation of vinyl macromers with metallocenes |
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 |
US8426659B2 (en) | 2011-03-25 | 2013-04-23 | Exxonmobil Chemical Patents Inc. | Vinyl terminated higher olefin polymers 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 |
US8399724B2 (en) | 2011-03-25 | 2013-03-19 | Exxonmobil Chemical Patents Inc. | Vinyl terminated higher olefin copolymers and methods to produce thereof |
US8669326B2 (en) | 2011-03-25 | 2014-03-11 | Exxonmobil Chemical Patents Inc. | Amine functionalized polyolefin and methods for preparation thereof |
US8669330B2 (en) | 2011-03-25 | 2014-03-11 | Exxonmobil Chemical Patents Inc. | Olefin triblock polymers via ring-opening metathesis polymerization |
US8835563B2 (en) | 2011-03-25 | 2014-09-16 | Exxonmobil Chemical Patents Inc. | Block copolymers from silylated vinyl terminated macromers |
US8785562B2 (en) | 2011-03-25 | 2014-07-22 | Exxonmobil Chemical Patents Inc. | Amphiphilic block polymers prepared by alkene metathesis |
US8809461B2 (en) | 2011-04-28 | 2014-08-19 | Braskem America, Inc. | Multimodal heterophasic copolymer and thermoformed articles from same |
WO2012155022A1 (en) | 2011-05-12 | 2012-11-15 | Dow Global Technologies Llc | Non-cyclopentadienyl-based chromium catalysts for olefin polymerization |
WO2013003541A1 (en) * | 2011-06-30 | 2013-01-03 | Dow Global Technologies Llc | Multilayered polyolefin-based films having a layer comprising a crystalline block copolymer composite or a block copolymer composite resin |
US8426521B2 (en) | 2011-07-20 | 2013-04-23 | The Procter & Gamble Company | Polymer composition |
AU2011374503B2 (en) | 2011-08-04 | 2016-04-07 | Prysmian S.P.A. | Energy cable having a thermoplastic electrically insulating layer |
US8445620B2 (en) | 2011-08-04 | 2013-05-21 | Exxonmobil Research And Engineering Company | Elastic propylene-alpha-olefin copolymer compositions and processes to produce them |
JP6164747B2 (ja) * | 2011-08-15 | 2017-07-19 | カルガリー サイエンティフィック インコーポレイテッド | 協働環境におけるフロー制御のためのおよび信頼性のある通信のための方法 |
US8530581B2 (en) | 2011-12-12 | 2013-09-10 | Exxonmobil Chemical Patents Inc. | Powder, compositions thereof, processes for making the same, and articles made therefrom |
US20130165354A1 (en) | 2011-12-22 | 2013-06-27 | Exxonmobil Research And Engineering Company | Method for improving engine fuel efficiency |
US9012578B2 (en) | 2012-04-19 | 2015-04-21 | Exxonmobil Chemical Patents Inc. | Blocky ethylene propylene copolymers and methods for making them |
US9676532B2 (en) | 2012-08-15 | 2017-06-13 | Avery Dennison Corporation | Packaging reclosure label for high alcohol content products |
US9322114B2 (en) | 2012-12-03 | 2016-04-26 | Exxonmobil Chemical Patents Inc. | Polypropylene fibers and fabrics |
WO2014088827A1 (en) | 2012-12-05 | 2014-06-12 | Exxonmobil Chemical Patents Inc. | Hdpe modified polyethylene blown film compositions having excellent bubble stability |
CN106113851A (zh) | 2012-12-18 | 2016-11-16 | 埃克森美孚化学专利公司 | 聚乙烯膜及其制造方法 |
US9422444B2 (en) | 2012-12-28 | 2016-08-23 | Dow Global Technologies Llc | Coating compositions |
JP6258968B2 (ja) | 2012-12-28 | 2018-01-10 | ダウ グローバル テクノロジーズ エルエルシー | コーティング組成物およびそれから作製される物品 |
WO2014185996A1 (en) | 2013-05-14 | 2014-11-20 | Exxonmobil Chemical Patents Inc. | Ethylene-based polymers and articles made therefrom |
WO2015047890A1 (en) | 2013-09-30 | 2015-04-02 | 3M Innovative Properties Company | Fibers and wipes with epoxidized fatty ester disposed thereon, and methods |
EP3052567A1 (en) | 2013-09-30 | 2016-08-10 | 3M Innovative Properties Company | Compositions, wipes, and methods |
KR20160062105A (ko) | 2013-09-30 | 2016-06-01 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 섬유, 와이프, 및 방법 |
WO2015074707A1 (en) | 2013-11-22 | 2015-05-28 | Trinseo Europe Gmbh | Polycarbonate containing compositions |
US10066102B2 (en) | 2013-11-22 | 2018-09-04 | Trinseo Europe Gmbh | Polycarbonate containing compositions |
WO2015085446A1 (en) | 2013-12-10 | 2015-06-18 | Exxonmobil Chemical Patents Inc. | Methods for making multilayer films and films made thereby |
US9315526B2 (en) | 2014-03-03 | 2016-04-19 | Exxonmobil Chemical Patents Inc. | Pyridyldiamido transition metal complexes, production and use thereof |
BR112016024633B1 (pt) | 2014-05-06 | 2022-05-03 | Basell Poliolefine Italia S.R.L. | Copolímeros de propileno-etileno aleatórios, processo para a preparação dos mesmos e artigos compreendendo os mesmos |
JP2017520642A (ja) | 2014-06-02 | 2017-07-27 | アベリー・デニソン・コーポレイションAvery Dennison Corporation | 耐スカッフ性、透明性、及び順応性が改善されたフィルム |
SG11201610684YA (en) | 2014-06-23 | 2017-01-27 | Dow Global Technologies Llc | Painted polyolefin articles |
BR112017003381A2 (pt) | 2014-08-21 | 2018-01-23 | Dow Global Technologies Llc | recipiente flexível e processo para a fabricação de um recipiente flexível |
WO2016053483A1 (en) | 2014-10-03 | 2016-04-07 | Exxonmobil Chemical Patents Inc. | Polyethylene polymers, films made therefrom, and methods of making the same |
WO2016069089A1 (en) | 2014-10-29 | 2016-05-06 | Exxonmobil Chemical Patents Inc. | Polyolefin adhesive compositions for elastic applications |
CN107108777B (zh) | 2014-11-12 | 2021-02-05 | 埃克森美孚化学专利公司 | 增塑剂的纯化及其在聚合物生产方法和装置中的用途 |
US10850484B2 (en) | 2015-03-17 | 2020-12-01 | Exxonmobil Chemical Patents Inc. | Multilayer films and methods of making the same |
EP3274381B1 (en) | 2015-04-20 | 2019-05-15 | ExxonMobil Chemical Patents Inc. | Catalyst composition comprising fluorided support and processes for use thereof |
US9487653B2 (en) | 2015-12-08 | 2016-11-08 | Exxonmobil Chemical Patents Inc. | Process of making crosslinked polyolefin polymer blends and compositions prepared thereof |
WO2017105614A1 (en) | 2015-12-16 | 2017-06-22 | Exxonmobil Chemical Patents Inc. | Low crystalline polymer compositions |
US10696027B2 (en) | 2016-03-11 | 2020-06-30 | Exxonmobil Chemical Patents, Inc. | Multilayer films and methods of making the same |
WO2017172102A1 (en) | 2016-03-31 | 2017-10-05 | Exxonmobil Chemical Patents Inc. | Low crystalline polymer compositions prepared in a dual reactor |
CN109071844A (zh) | 2016-04-22 | 2018-12-21 | 埃克森美孚化学专利公司 | 聚乙烯片材 |
CN109641990B (zh) | 2016-07-13 | 2022-08-19 | 埃克森美孚化学专利公司 | 双金属茂催化剂共聚物组合物 |
US11352451B2 (en) | 2016-07-13 | 2022-06-07 | Exxonmobil Chemical Patents Inc. | Dual metallocene catalyst copolymer compositions |
US11299567B2 (en) | 2016-07-14 | 2022-04-12 | Exxonmobil Chemical Patents Inc. | Lubricating oil compositions comprising dual metallocene-catalyzed bimodal copolymer compositions useful as viscosity modifiers |
WO2018022263A1 (en) | 2016-07-29 | 2018-02-01 | Exxonmobil Chemical Patents Inc. | Polymerization processes using high molecular weight polyhydric quenching agents |
WO2018102091A1 (en) | 2016-12-02 | 2018-06-07 | Exxonmobil Chemical Patents Inc. | Polyethylene films |
WO2018106480A1 (en) | 2016-12-06 | 2018-06-14 | Exxonmobil Chemical Patents Inc. | Multilayer films and methods of making the same |
US10584297B2 (en) | 2016-12-13 | 2020-03-10 | Afton Chemical Corporation | Polyolefin-derived dispersants |
US10221267B2 (en) | 2016-12-13 | 2019-03-05 | Afton Chemical Corporation | Microstructure-controlled copolymers of ethylene and C3-C10 alpha-olefins |
WO2018151903A1 (en) | 2017-02-20 | 2018-08-23 | Exxonmobil Chemical Patents Inc. | Supported catalyst systems and processes for use thereof |
MX2019011918A (es) * | 2017-04-04 | 2019-11-18 | Braskem America Inc | Copolimero aleatorio de alto etileno con oligomeros no migratorios. |
US20200108539A1 (en) | 2017-04-06 | 2020-04-09 | ExxonMobil Chemica Patents Inc. | Cast Films and Processes for Making the Same |
WO2018194740A1 (en) | 2017-04-19 | 2018-10-25 | Exxonmobil Chemical Patents Inc. | Multilayer films and methods of making the same |
US11244815B2 (en) | 2017-04-20 | 2022-02-08 | Honeywell International Inc. | Profiled sputtering target and method of making the same |
WO2018226311A1 (en) | 2017-06-08 | 2018-12-13 | Exxonmobil Chemical Patents Inc. | Polyethylene blends and extrudates and methods of making the same |
EP3638730B1 (en) | 2017-06-14 | 2024-05-01 | ExxonMobil Chemical Patents Inc. | Ethylene copolymer blends for cross-linking applications |
SG11201910691TA (en) | 2017-07-06 | 2020-01-30 | Exxonmobil Chemical Patents Inc | Polyethylene compositions comprising cyclic-olefin copolymers |
WO2019027524A1 (en) | 2017-08-02 | 2019-02-07 | Exxonmobil Chemical Patents Inc. | MULTILAYER FILMS AND METHODS OF MANUFACTURE |
WO2019027586A1 (en) | 2017-08-04 | 2019-02-07 | Exxonmobil Chemical Patents Inc. | MIXED CATALYSTS COMPRISING 2,6-BIS (IMINO) PYRIDYL-IRON COMPLEXES AND BRONZED HAFNOCENES |
WO2019027587A1 (en) | 2017-08-04 | 2019-02-07 | Exxonmobil Chemical Patents Inc. | POLYETHYLENE COMPOSITIONS AND FILMS PREPARED THEREFROM |
EP3697822A4 (en) | 2017-08-04 | 2020-08-26 | ExxonMobil Chemical Patents Inc. | MIXED CATALYSTS INCLUDING UNBRIDGED HAFNOCENE WITH -CH2-SIME3 FRACTIONS |
EP3661984B1 (en) | 2017-08-04 | 2022-01-19 | ExxonMobil Chemical Patents Inc. | Films made from polyethylene compositions and processes for making the same |
US11512191B2 (en) * | 2017-11-10 | 2022-11-29 | Avient Corporation | Polyolefin elastomer blends for elastomeric films |
JP7118623B2 (ja) | 2017-11-17 | 2022-08-16 | 花王株式会社 | 不織布の製造方法 |
WO2019108326A1 (en) | 2017-11-28 | 2019-06-06 | Exxonmobil Chemical Patents Inc. | Multilayer films and methods of making the same |
KR102405495B1 (ko) | 2017-12-01 | 2022-06-08 | 엑손모빌 케미칼 패턴츠 인코포레이티드 | 촉매계 및 이를 사용하기 위한 중합 방법 |
WO2019108327A1 (en) | 2017-12-01 | 2019-06-06 | Exxonmobil Chemical Patents Inc. | Films comprising polyethylene composition |
WO2019162760A1 (en) | 2018-02-05 | 2019-08-29 | Exxonmobil Chemical Patents Inc. A Corporation Of State Of Delaware | Enhanced processability of lldpe by addition of ultra-high molecular weight high density polyethylene |
WO2019156802A1 (en) | 2018-02-12 | 2019-08-15 | Exxonmobil Chemical Patents Inc. | Metallocene catalyst feed system for solution polymerization process |
US11241868B2 (en) | 2018-02-27 | 2022-02-08 | Inteplast Group Corporation | Clear film for tapes and labels |
WO2019240899A1 (en) | 2018-06-13 | 2019-12-19 | Exxonmobil Chemical Patents Inc. | Polyolefin blend compositions |
EP3810666A1 (en) | 2018-06-19 | 2021-04-28 | ExxonMobil Chemical Patents Inc. | Polyethylene compositions and films prepared therefrom |
WO2020046597A1 (en) | 2018-08-29 | 2020-03-05 | Exxonmobil Chemical Patents Inc. | Methods of making polymer compositions with enhanced elasticity by employing vtp and hmp catalyst systems in parallel processes |
WO2020068497A1 (en) | 2018-09-25 | 2020-04-02 | Exxonmobil Chemical Patents Inc. | Multilayer films and methods of making the same |
CA3116210A1 (en) * | 2018-10-12 | 2020-04-16 | Berry Global, Inc. | Machine direction-oriented polymeric film, and method of making the machine direction-oriented polymeric film |
WO2020092597A1 (en) | 2018-11-01 | 2020-05-07 | Exxonmobil Chemical Patents Inc. | On-line adjustment of catalysts by trim and olefin polymerization |
CN112969724B (zh) | 2018-11-01 | 2023-03-21 | 埃克森美孚化学专利公司 | 混合催化剂比的在线调节和烯烃聚合 |
CN112969723B (zh) | 2018-11-01 | 2023-04-28 | 埃克森美孚化学专利公司 | 通过修整的混合催化剂比的在线调节和使用其的烯烃聚合 |
US20220056168A1 (en) | 2018-11-01 | 2022-02-24 | Exxonmobil Chemical Patents Inc. | Slurry Trim Feeder Modifications |
US11976140B2 (en) | 2018-11-01 | 2024-05-07 | Exxonmobil Chemical Patents Inc. | In-line trimming of dry catalyst feed |
WO2020139499A1 (en) | 2018-12-26 | 2020-07-02 | Exxonmobil Chemical Patents Inc. | Multilayer metallized cast polypropylene films doped with hydrocarbon resin |
US20220152906A1 (en) | 2019-02-13 | 2022-05-19 | Exxonmobil Chemical Patents Inc. | Oriented Multilayer Polyethylene Films and Laminates Thereof |
WO2020167929A1 (en) | 2019-02-13 | 2020-08-20 | Exxonmobil Chemical Patents Inc. | Methods for making films and films made thereby |
WO2020190507A1 (en) | 2019-03-19 | 2020-09-24 | Exxonmobil Chemical Patents Inc. | Multilayer oriented films |
CN113646074B (zh) | 2019-04-05 | 2023-05-09 | 埃克森美孚化学专利公司 | 控制聚烯烃产物的分子量分布和化学组成分布 |
US11530279B2 (en) | 2019-04-05 | 2022-12-20 | Exxonmobil Chemicals Patents Inc. | Broad molecular weight distribution polymer product from loop reactors with intentional thermal gradients |
SG11202110446QA (en) | 2019-04-05 | 2021-10-28 | Exxonmobil Chemical Patents Inc | Broad molecular weight distribution polymer product from loop reactors with intentional thermal gradients |
AR118648A1 (es) | 2019-04-24 | 2021-10-20 | Dow Global Technologies Llc | Película multicapa de funda estirable con resistencia al desgarro mejorada |
CN113272310A (zh) * | 2019-04-26 | 2021-08-17 | Lg化学株式会社 | 配体化合物,过渡金属化合物和包含其的催化剂组合物 |
WO2020242912A1 (en) | 2019-05-24 | 2020-12-03 | Eastman Chemical Company | Blend small amounts of pyoil into a liquid stream processed into a gas cracker |
WO2021011638A1 (en) * | 2019-07-18 | 2021-01-21 | Exxonmobil Chemical Patents Inc. | Silyl-bridged pyridylamide catalysts and methods thereof |
WO2021034471A1 (en) | 2019-08-16 | 2021-02-25 | Exxonmobil Chemical Patents Inc. | Producing blocks of block copolymer in a separator downstream of a reactor |
WO2021034400A1 (en) | 2019-08-20 | 2021-02-25 | Exxonmobil Chemical Patents Inc. | Films and methods of making the same |
JP2021059387A (ja) * | 2019-10-09 | 2021-04-15 | 昭和電工パッケージング株式会社 | 油脂含有食品収容用の成形容器及び包装体 |
WO2021080813A1 (en) | 2019-10-22 | 2021-04-29 | Exxonmobil Chemical Patents Inc. | Thermoplastic vulcanizate compositions and processes for the production thereof |
WO2021080803A1 (en) | 2019-10-22 | 2021-04-29 | Exxonmobil Chemical Patents Inc. | Impact copolymer compositions |
WO2021086552A1 (en) | 2019-10-29 | 2021-05-06 | Exxonmobil Chemical Patents Inc. | Production of gradient copolymers using monomer and comonomer concentration gradients in a loop reactor |
US11945998B2 (en) | 2019-10-31 | 2024-04-02 | Eastman Chemical Company | Processes and systems for making recycle content hydrocarbons |
EP4054997A4 (en) | 2019-11-07 | 2024-02-21 | Eastman Chem Co | ALPHA-OLEFINS AND FAT ALCOHOLS WITH RECYCLING CONTENT |
JP7075921B2 (ja) * | 2019-12-27 | 2022-05-26 | 株式会社アシックス | 緩衝体及び靴 |
EP4106994A1 (en) | 2020-02-18 | 2022-12-28 | ExxonMobil Chemical Patents Inc. | High tenacity handwrap stretch film for improved pallet stability |
WO2021195070A1 (en) | 2020-03-26 | 2021-09-30 | Exxonmobil Chemical Patents Inc. | Processes for making 3-d objects from blends of polypropylene and semi-amorphous polymers |
JP7476337B2 (ja) * | 2020-10-06 | 2024-04-30 | 三井化学株式会社 | 樹脂組成物 |
CN116917353A (zh) | 2021-03-05 | 2023-10-20 | 埃克森美孚化学专利公司 | 制备和使用淤浆催化剂混合物的方法 |
Family Cites Families (137)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US515203A (en) * | 1894-02-20 | Support for spinning-spindles | ||
US748846A (en) * | 1904-01-05 | Robert r | ||
US593083A (en) * | 1897-11-02 | Thomas m | ||
US628343A (en) * | 1899-02-27 | 1899-07-04 | Werner Menzel | Fixing of insulators for carrying electric-line wires. |
US663422A (en) * | 1900-08-11 | 1900-12-11 | Steel Cable Engineering Company | Hopper-delivery mechanism. |
US676421A (en) * | 1900-09-27 | 1901-06-18 | David P Clark | Locomotive toy. |
US683176A (en) * | 1900-10-16 | 1901-09-24 | Frank Marshall Ho-Glen | Binder. |
US728772A (en) * | 1901-01-03 | 1903-05-19 | Leopoldo Sconfietti | Moistening, cooling, or heating the air in factories, workrooms, or the like. |
US692500A (en) * | 1901-01-15 | 1902-02-04 | George W Barnett | Display-rack. |
US699213A (en) * | 1901-10-03 | 1902-05-06 | James Mossman | Combined wire stretcher, cutter, splicer, and staple-puller. |
US697420A (en) * | 1901-10-19 | 1902-04-08 | Kempshall Mfg Co | Golf-ball. |
US728150A (en) * | 1901-12-07 | 1903-05-12 | William R Wolf | Sectional bookcase. |
US721798A (en) * | 1901-12-31 | 1903-03-03 | Fredrick Hagen | Snapping-rolls for corn-husking machines. |
US716121A (en) * | 1902-01-02 | 1902-12-16 | Charles William Sievert | Oil-burner. |
US735058A (en) * | 1902-05-19 | 1903-08-04 | Thaddeus M Boggs | Brick-machine. |
US728771A (en) * | 1902-08-20 | 1903-05-19 | James B Schuman | Grain-elevator. |
US728151A (en) * | 1903-02-12 | 1903-05-12 | Carl Baeker | Time-fuse for artillery projectiles. |
US780404A (en) * | 1903-09-22 | 1905-01-17 | Basf Ag | Process of oxidizing methyl groups in aromatic hydrocarbons. |
US2051634A (en) * | 1931-10-22 | 1936-08-18 | Johns Manville | Pipe wrapping machine |
US2051928A (en) * | 1934-11-30 | 1936-08-25 | Anaconda Copper Mining Co | Electrodeposition |
USB632416I5 (US20030194575A1-20031016-C00022.png) * | 1956-03-01 | 1976-03-09 | ||
US3520861A (en) * | 1968-12-26 | 1970-07-21 | Dow Chemical Co | Copolymers of ethylene |
US4237190A (en) * | 1977-09-26 | 1980-12-02 | American Can Company | Propylene/polystyrene composition and substrates coated with such compositions |
DE3127133A1 (de) * | 1981-07-09 | 1983-01-27 | Hoechst Ag, 6000 Frankfurt | Verfahren zur herstellung von polyolefinen und deren copolymerisaten |
US4543399A (en) * | 1982-03-24 | 1985-09-24 | Union Carbide Corporation | Fluidized bed reaction systems |
US4588790A (en) * | 1982-03-24 | 1986-05-13 | Union Carbide Corporation | Method for fluidized bed polymerization |
DE3240383A1 (de) * | 1982-11-02 | 1984-05-03 | Hoechst Ag, 6230 Frankfurt | Verfahren zur herstellung von oligomeren aluminoxanen |
US5324800A (en) * | 1983-06-06 | 1994-06-28 | Exxon Chemical Patents Inc. | Process and catalyst for polyolefin density and molecular weight control |
US4599392A (en) * | 1983-06-13 | 1986-07-08 | The Dow Chemical Company | Interpolymers of ethylene and unsaturated carboxylic acids |
AU602873B2 (en) * | 1985-11-29 | 1990-11-01 | American National Can Company | Films using blends of polypropylene and polyisobutylene |
US5198401A (en) * | 1987-01-30 | 1993-03-30 | Exxon Chemical Patents Inc. | Ionic metallocene catalyst compositions |
US5153157A (en) * | 1987-01-30 | 1992-10-06 | Exxon Chemical Patents Inc. | Catalyst system of enhanced productivity |
PL276385A1 (en) | 1987-01-30 | 1989-07-24 | Exxon Chemical Patents Inc | Method for polymerization of olefines,diolefins and acetylene unsaturated compounds |
US5408017A (en) * | 1987-01-30 | 1995-04-18 | Exxon Chemical Patents Inc. | High temperature polymerization process using ionic catalysts to produce polyolefins |
IL85097A (en) | 1987-01-30 | 1992-02-16 | Exxon Chemical Patents Inc | Catalysts based on derivatives of a bis(cyclopentadienyl)group ivb metal compound,their preparation and their use in polymerization processes |
US5096867A (en) * | 1990-06-04 | 1992-03-17 | Exxon Chemical Patents Inc. | Monocyclopentadienyl transition metal olefin polymerization catalysts |
US5384299A (en) * | 1987-01-30 | 1995-01-24 | Exxon Chemical Patents Inc. | Ionic metallocene catalyst compositions |
US4874880A (en) * | 1987-03-10 | 1989-10-17 | Chisso Corporation | Bis(di-, tri- or tetra-substituted-cyclopentadienyl)-zirconium dihalides |
US4988781A (en) * | 1989-02-27 | 1991-01-29 | The Dow Chemical Company | Process for producing homogeneous modified copolymers of ethylene/alpha-olefin carboxylic acids or esters |
US5093415A (en) * | 1987-05-19 | 1992-03-03 | Union Carbide Chemicals & Plastics Technology Corporation | Process for producing stereoregular polymers having a narrow molecular weight distribution |
US5015749A (en) * | 1987-08-31 | 1991-05-14 | The Dow Chemical Company | Preparation of polyhydrocarbyl-aluminoxanes |
FR2634212B1 (fr) * | 1988-07-15 | 1991-04-19 | Bp Chimie Sa | Appareillage et procede de polymerisation d'olefines en phase gazeuse dans un reacteur a lit fluidise |
US5041584A (en) * | 1988-12-02 | 1991-08-20 | Texas Alkyls, Inc. | Modified methylaluminoxane |
US4960878A (en) * | 1988-12-02 | 1990-10-02 | Texas Alkyls, Inc. | Synthesis of methylaluminoxanes |
US5218071A (en) * | 1988-12-26 | 1993-06-08 | Mitsui Petrochemical Industries, Ltd. | Ethylene random copolymers |
ES2148147T3 (es) * | 1989-02-27 | 2000-10-16 | Dow Chemical Co | Procedimiento para producir copolimeros modificados homogeneos de etileno/acidos carboxilicos de alfa-olefinas o sus esteres. |
NZ235032A (en) * | 1989-08-31 | 1993-04-28 | Dow Chemical Co | Constrained geometry complexes of titanium, zirconium or hafnium comprising a substituted cyclopentadiene ligand; use as olefin polymerisation catalyst component |
US5057475A (en) * | 1989-09-13 | 1991-10-15 | Exxon Chemical Patents Inc. | Mono-Cp heteroatom containing group IVB transition metal complexes with MAO: supported catalyst for olefin polymerization |
US5064802A (en) * | 1989-09-14 | 1991-11-12 | The Dow Chemical Company | Metal complex compounds |
FR2656314B1 (fr) * | 1989-12-22 | 1992-04-17 | Bp Chemicals Snc | Catalyseur a base de zirconium supporte sur du chlorure de magnesium, procede de preparation et utilisation du catalyseur dans la polymerisation des olefines. |
US5032562A (en) * | 1989-12-27 | 1991-07-16 | Mobil Oil Corporation | Catalyst composition and process for polymerizing polymers having multimodal molecular weight distribution |
US5044438A (en) * | 1990-03-16 | 1991-09-03 | Young Joe A | Wellhead bowl protector and retrieving tool |
US5200131A (en) * | 1990-04-09 | 1993-04-06 | Mitsui Toatsu Chemicals, Inc. | Method for molding syndiotactic polypropylene |
US5041585A (en) * | 1990-06-08 | 1991-08-20 | Texas Alkyls, Inc. | Preparation of aluminoxanes |
US5041583A (en) * | 1990-06-28 | 1991-08-20 | Ethyl Corporation | Preparation of aluminoxanes |
JP2545006B2 (ja) | 1990-07-03 | 1996-10-16 | ザ ダウ ケミカル カンパニー | 付加重合触媒 |
US5272236A (en) * | 1991-10-15 | 1993-12-21 | The Dow Chemical Company | Elastic substantially linear olefin polymers |
US5134209A (en) * | 1990-12-26 | 1992-07-28 | Shell Oil Company | Process of producing ethylene-propylene rubbery copolymer |
EP0499216B1 (en) * | 1991-02-15 | 1998-01-07 | MITSUI TOATSU CHEMICALS, Inc. | Transparent impact-resistant molded articles |
JP3275211B2 (ja) | 1991-05-20 | 2002-04-15 | ザ ダウ ケミカル カンパニー | 付加重合触媒の製造方法 |
CA2067451A1 (en) | 1991-05-24 | 1993-10-29 | Gregory B. Kharas | Polylactide blends |
US5721185A (en) * | 1991-06-24 | 1998-02-24 | The Dow Chemical Company | Homogeneous olefin polymerization catalyst by abstraction with lewis acids |
US5710224A (en) * | 1991-07-23 | 1998-01-20 | Phillips Petroleum Company | Method for producing polymer of ethylene |
US5525695A (en) * | 1991-10-15 | 1996-06-11 | The Dow Chemical Company | Elastic linear interpolymers |
US5278272A (en) * | 1991-10-15 | 1994-01-11 | The Dow Chemical Company | Elastic substantialy linear olefin polymers |
ES2108861T3 (es) * | 1991-11-25 | 1998-01-01 | Exxon Chemical Patents Inc | Composiciones cataliticas polionicas de metales de transicion. |
US5436304A (en) * | 1992-03-19 | 1995-07-25 | Exxon Chemical Patents Inc. | Process for polymerizing monomers in fluidized beds |
US5352749A (en) * | 1992-03-19 | 1994-10-04 | Exxon Chemical Patents, Inc. | Process for polymerizing monomers in fluidized beds |
US5296433A (en) * | 1992-04-14 | 1994-03-22 | Minnesota Mining And Manufacturing Company | Tris(pentafluorophenyl)borane complexes and catalysts derived therefrom |
US5350723A (en) * | 1992-05-15 | 1994-09-27 | The Dow Chemical Company | Process for preparation of monocyclopentadienyl metal complex compounds and method of use |
DE69326463T2 (de) * | 1992-07-01 | 2000-05-04 | Exxon Chemical Patents Inc | Olefinpolymerisationskatalysatoren auf basis von uebergangsmetallen |
US5317036A (en) | 1992-10-16 | 1994-05-31 | Union Carbide Chemicals & Plastics Technology Corporation | Gas phase polymerization reactions utilizing soluble unsupported catalysts |
US5332706A (en) * | 1992-12-28 | 1994-07-26 | Mobil Oil Corporation | Process and a catalyst for preventing reactor fouling |
US5608019A (en) * | 1992-12-28 | 1997-03-04 | Mobil Oil Corporation | Temperature control of MW in olefin polymerization using supported metallocene catalyst |
US5462999A (en) * | 1993-04-26 | 1995-10-31 | Exxon Chemical Patents Inc. | Process for polymerizing monomers in fluidized beds |
WO1994025495A1 (en) * | 1993-05-20 | 1994-11-10 | Exxon Chemical Patents Inc. | Process for polymerizing monomers in fluidized beds |
US5883188A (en) * | 1993-04-28 | 1999-03-16 | The Dow Chemical Company | Paintable olefinic interpolymer compositions |
FR2705252B1 (fr) * | 1993-05-19 | 1995-07-21 | Bp Chemicals Snc | Procédé d'introduction d'un solide dans un réacteur et appareillage. |
ZA943399B (en) * | 1993-05-20 | 1995-11-17 | Bp Chem Int Ltd | Polymerisation process |
CA2125246C (en) * | 1993-06-07 | 2001-07-03 | Junichi Imuta | Transition metal compound and olefin polymerization catalyst using the same |
EP0705269B1 (en) * | 1993-06-24 | 1997-01-15 | The Dow Chemical Company | Titanium(ii) or zirconium(ii) complexes and addition polymerization catalysts therefrom |
US5504223A (en) * | 1994-01-25 | 1996-04-02 | The Dow Chemical Company | Synthesis of cyclopentadienyl metal coordination complexes from metal hydrocarbyloxides |
DE4416876A1 (de) * | 1994-05-13 | 1995-11-16 | Basf Ag | Verfahren zur Herstellung von verbrückten Halbsandwichkomplexen |
US5461123A (en) * | 1994-07-14 | 1995-10-24 | Union Carbide Chemicals & Plastics Technology Corporation | Gas phase fluidized bed polyolefin polymerization process using sound waves |
US5972822A (en) * | 1994-08-02 | 1999-10-26 | The Dow Chemical Company | Biscyclopentadienyldiene complex containing addition polymerization catalysts |
US5453471B1 (en) * | 1994-08-02 | 1999-02-09 | Carbide Chemicals & Plastics T | Gas phase polymerization process |
US5625087A (en) * | 1994-09-12 | 1997-04-29 | The Dow Chemical Company | Silylium cationic polymerization activators for metallocene complexes |
CA2164461C (en) * | 1994-12-06 | 2000-08-08 | Tatsuya Tanizaki | Polypropylene composition and uses thereof |
US5616661A (en) * | 1995-03-31 | 1997-04-01 | Union Carbide Chemicals & Plastics Technology Corporation | Process for controlling particle growth during production of sticky polymers |
US5637660A (en) * | 1995-04-17 | 1997-06-10 | Lyondell Petrochemical Company | Polymerization of α-olefins with transition metal catalysts based on bidentate ligands containing pyridine or quinoline moiety |
US5731253A (en) * | 1995-07-27 | 1998-03-24 | Albemarle Corporation | Hydrocarbylsilloxy - aluminoxane compositions |
US5962714A (en) * | 1995-10-02 | 1999-10-05 | Mccullough; Laughlin Gerard | Monocyclopentadienyl transition metal catalyst and olefin polymerization process |
US5728855A (en) * | 1995-10-19 | 1998-03-17 | Akzo Nobel Nv | Modified polyalkylaluminoxane composition formed using reagent containing carbon-oxygen double bond |
US5767208A (en) * | 1995-10-20 | 1998-06-16 | Exxon Chemical Patents Inc. | High temperature olefin polymerization process |
AU1685597A (en) * | 1996-01-26 | 1997-08-20 | Dow Chemical Company, The | Improved olefin addition polymerization catalyst composition |
DE69702506T2 (de) * | 1996-03-27 | 2001-03-08 | Dow Chemical Co | Hochlösliches aktivierungsmittel für olefinpolymerisationskatalysator |
CN1214698A (zh) * | 1996-03-27 | 1999-04-21 | 陶氏化学公司 | 采用分散的催化剂活化剂进行的溶液聚合方法 |
US5977251A (en) * | 1996-04-01 | 1999-11-02 | The Dow Chemical Company | Non-adiabatic olefin solution polymerization |
WO1998003520A1 (en) * | 1996-07-22 | 1998-01-29 | The Dow Chemical Company | Metal complexes containing bridged, non-aromatic, anionic, dienyl groups and addition polymerization catalysts therefrom |
SK15399A3 (en) * | 1996-08-08 | 2000-04-10 | Dow Chemical Co | 3-heteroatom substituted cyclopentadienyl-containing metal complexes and olefin polymerization process |
US6015868A (en) * | 1996-10-03 | 2000-01-18 | The Dow Chemical Company | Substituted indenyl containing metal complexes and olefin polymerization process |
TW442528B (en) * | 1996-12-02 | 2001-06-23 | Chisso Corp | Polypropylene composition |
US6245856B1 (en) * | 1996-12-17 | 2001-06-12 | Exxon Chemical Patents, Inc. | Thermoplastic olefin compositions |
CN1195797C (zh) * | 1996-12-17 | 2005-04-06 | 高级弹性体系统两合公司 | 热塑性弹性组合物 |
US5965756A (en) * | 1996-12-19 | 1999-10-12 | The Dow Chemical Company | Fused ring substituted indenyl metal complexes and polymerization process |
US6103657A (en) * | 1997-07-02 | 2000-08-15 | Union Carbide Chemicals & Plastics Technology Corporation | Catalyst for the production of olefin polymers |
CA2210131C (en) * | 1997-07-09 | 2005-08-02 | Douglas W. Stephan | Supported phosphinimine-cp catalysts |
US6921794B2 (en) * | 1997-08-12 | 2005-07-26 | Exxonmobil Chemical Patents Inc. | Blends made from propylene ethylene polymers |
US6635715B1 (en) * | 1997-08-12 | 2003-10-21 | Sudhin Datta | Thermoplastic polymer blends of isotactic polypropylene and alpha-olefin/propylene copolymers |
US6525157B2 (en) | 1997-08-12 | 2003-02-25 | Exxonmobile Chemical Patents Inc. | Propylene ethylene polymers |
US6150297A (en) * | 1997-09-15 | 2000-11-21 | The Dow Chemical Company | Cyclopentaphenanthrenyl metal complexes and polymerization process |
US6197910B1 (en) * | 1997-12-10 | 2001-03-06 | Exxon Chemical Patents, Inc. | Propylene polymers incorporating macromers |
EA200000905A1 (ru) * | 1998-03-04 | 2001-04-23 | Эксон Кемикэл Пейтентс Инк. | Продукт и способ получения полиолефиновых дисперсий |
US6034240A (en) * | 1998-03-09 | 2000-03-07 | Symyx Technologies, Inc. | Substituted aminomethylphosphines, coordination complexes of aminomethylphosphines and their synthesis |
DE19812229A1 (de) * | 1998-03-20 | 1999-09-23 | Basf Ag | Polymere des Propens |
US6288171B2 (en) * | 1998-07-01 | 2001-09-11 | Advanced Elastomer Systems, L.P. | Modification of thermoplastic vulcanizates using random propylene copolymers |
EP1522553B1 (en) * | 1998-07-01 | 2007-04-11 | ExxonMobil Chemical Patents Inc. | Elastic blends comprising crystalline polymer and crystallizable polymers of propylene |
KR20010072663A (ko) * | 1998-07-02 | 2001-07-31 | 엑손 케미칼 패턴츠 인코포레이티드 | 프로필렌 올레핀 공중합체 |
US6303719B1 (en) * | 1998-12-18 | 2001-10-16 | Univation Technologies | Olefin polymerization catalyst system |
AU4186500A (en) * | 1999-04-01 | 2000-10-23 | Symyx Technologies, Inc. | Polymerization catalyst ligands, catalytic metal complexes and compositions and processes using and methods of making same |
DE60040697D1 (de) * | 1999-05-13 | 2008-12-11 | Exxonmobil Chem Patents Inc | Elastische Fasern und daraus hergestellte Artikel, die kristalline und kristallisierbare Propylenpolymere enthalten |
US6500563B1 (en) * | 1999-05-13 | 2002-12-31 | Exxonmobil Chemical Patents Inc. | Elastic films including crystalline polymer and crystallizable polymers of propylene |
US6750284B1 (en) * | 1999-05-13 | 2004-06-15 | Exxonmobil Chemical Patents Inc. | Thermoplastic filled membranes of propylene copolymers |
CA2372278A1 (en) * | 1999-05-19 | 2000-11-23 | Exxon Chemical Patents, Inc. | Isobutylene based elastomer blends having improved strength, elasticity, and reduced permeability |
CN1209404C (zh) * | 1999-09-01 | 2005-07-06 | 埃克森化学专利公司 | 透气膜及其制备方法 |
US6825295B2 (en) * | 1999-12-10 | 2004-11-30 | Dow Global Technologies Inc. | Alkaryl-substituted group 4 metal complexes, catalysts and olefin polymerization process |
KR100714508B1 (ko) * | 1999-12-10 | 2007-05-07 | 다우 글로벌 테크놀로지스 인크. | 치환된 4족 금속 착체, 촉매 및 올레핀 중합 방법 |
US20020165329A1 (en) * | 1999-12-10 | 2002-11-07 | Jerzy Klosin | Alkylphenyl-substituted group 4 metal complexes, catalysts and olefin polymerization process |
CN1333032C (zh) * | 1999-12-22 | 2007-08-22 | 埃克森美孚化学专利公司 | 聚丙烯基粘合剂组合物 |
US20020049288A1 (en) * | 2000-04-04 | 2002-04-25 | Christopher Goh | Ether-amine based polymerization catalysts, compositions and processes using same |
WO2002002577A1 (en) * | 2000-06-30 | 2002-01-10 | Dow Global Technology Inc. | Polycyclic, fused ring compounds, metal complexes and polymerization process |
US6727361B2 (en) * | 2000-11-07 | 2004-04-27 | Symyx Technologies, Inc. | Phosphino substituted pyridine amine ligands |
CA2432916A1 (en) | 2000-12-22 | 2002-07-04 | Exxonmobil Chemical Patents Inc. | Composites comprising semicrystalline random ethylene / propylenecopolymers |
KR20030064415A (ko) | 2000-12-22 | 2003-07-31 | 엑손모빌 케미칼 패턴츠 인코포레이티드 | 다성분계 고분자 구조체 |
WO2004035681A2 (en) | 2002-10-17 | 2004-04-29 | Exxonmobil Chemical Patents Inc. | Hetero phase polymer compositions |
AU2003297134A1 (en) | 2002-12-17 | 2004-07-29 | Exxonmobil Chemical Patents Inc. | Elastic blends comprising elastic crystalline polymer and crystallizable polymers for ethylene |
JP4644656B2 (ja) | 2003-01-08 | 2011-03-02 | エクソンモービル・ケミカル・パテンツ・インク | 弾性製品及びその製造方法 |
-
2002
- 2002-05-06 EP EP02725927A patent/EP1444276A1/en not_active Withdrawn
- 2002-05-06 WO PCT/US2002/014158 patent/WO2003040201A1/en active Application Filing
- 2002-05-06 JP JP2003542246A patent/JP2005508415A/ja active Pending
- 2002-05-06 SG SG200602838-5A patent/SG147306A1/en unknown
- 2002-11-05 CN CN200810131872.6A patent/CN101319071B/zh not_active Expired - Fee Related
- 2002-11-05 US US10/289,168 patent/US7041765B2/en not_active Expired - Lifetime
- 2002-11-05 CN CN200810131873.0A patent/CN101319050A/zh active Pending
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- 2003-08-15 US US10/641,978 patent/US6919407B2/en not_active Expired - Lifetime
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- 2004-10-18 US US10/967,849 patent/US6946535B2/en not_active Expired - Lifetime
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- 2005-08-31 US US11/216,805 patent/US20060004167A1/en not_active Abandoned
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CN105500870A (zh) * | 2009-04-15 | 2016-04-20 | 金达胶片美国有限责任公司 | 薄膜组合物和制造该薄膜组合物的方法 |
CN110099933A (zh) * | 2016-12-29 | 2019-08-06 | 北欧化工公司 | 用于制造聚丙烯组合物的方法 |
CN110099933B (zh) * | 2016-12-29 | 2023-09-15 | 北欧化工公司 | 用于制造聚丙烯组合物的方法 |
CN110770262A (zh) * | 2017-11-17 | 2020-02-07 | 东邦钛株式会社 | 烯烃类聚合用固体催化剂成分、烯烃类聚合用固体催化剂成分的制造方法、烯烃类聚合用催化剂和烯烃类聚合物的制造方法 |
CN110770262B (zh) * | 2017-11-17 | 2023-05-23 | 东邦钛株式会社 | 烯烃类聚合用固体催化剂成分及其制造方法、烯烃类聚合用催化剂和烯烃类聚合物制造方法 |
CN114728991A (zh) * | 2020-04-16 | 2022-07-08 | 株式会社Lg化学 | 配体化合物、过渡金属化合物和包含其的催化剂组合物 |
Also Published As
Publication number | Publication date |
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EP1444276A1 (en) | 2004-08-11 |
JP2005508415A (ja) | 2005-03-31 |
US20060004167A1 (en) | 2006-01-05 |
US20070249798A1 (en) | 2007-10-25 |
CN101319071B (zh) | 2011-08-17 |
US6919407B2 (en) | 2005-07-19 |
SG147306A1 (en) | 2008-11-28 |
US20030194575A1 (en) | 2003-10-16 |
US6946535B2 (en) | 2005-09-20 |
US7897679B2 (en) | 2011-03-01 |
US7041765B2 (en) | 2006-05-09 |
CN101319071A (zh) | 2008-12-10 |
WO2003040201A1 (en) | 2003-05-15 |
US20040082750A1 (en) | 2004-04-29 |
US20050054800A1 (en) | 2005-03-10 |
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Effective date of abandoning: 20081210 |
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C20 | Patent right or utility model deemed to be abandoned or is abandoned |