JP2002528575A - オレフィンの重合方法、新規ポリエチレン並びにそれから製造されるフィルム及び物品 - Google Patents
オレフィンの重合方法、新規ポリエチレン並びにそれから製造されるフィルム及び物品Info
- Publication number
- JP2002528575A JP2002528575A JP2000578359A JP2000578359A JP2002528575A JP 2002528575 A JP2002528575 A JP 2002528575A JP 2000578359 A JP2000578359 A JP 2000578359A JP 2000578359 A JP2000578359 A JP 2000578359A JP 2002528575 A JP2002528575 A JP 2002528575A
- Authority
- JP
- Japan
- Prior art keywords
- hydrogen atoms
- group containing
- hydrogen
- groups
- less
- 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.)
- Withdrawn
Links
- -1 polyethylene Polymers 0.000 title claims abstract description 90
- 238000006116 polymerization reaction Methods 0.000 title claims abstract description 54
- 150000001336 alkenes Chemical class 0.000 title claims abstract description 39
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 title claims abstract description 24
- 229920000573 polyethylene Polymers 0.000 title abstract description 46
- 239000004698 Polyethylene Substances 0.000 title abstract description 45
- 238000000034 method Methods 0.000 claims abstract description 87
- 150000001875 compounds Chemical class 0.000 claims abstract description 80
- 238000009826 distribution Methods 0.000 claims abstract description 31
- 239000003054 catalyst Substances 0.000 claims abstract description 30
- 239000011954 Ziegler–Natta catalyst Substances 0.000 claims abstract description 14
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 351
- 229910052739 hydrogen Inorganic materials 0.000 claims description 65
- 229910052736 halogen Inorganic materials 0.000 claims description 64
- 125000000217 alkyl group Chemical group 0.000 claims description 63
- 239000001257 hydrogen Substances 0.000 claims description 62
- 150000002367 halogens Chemical class 0.000 claims description 61
- 125000003118 aryl group Chemical group 0.000 claims description 60
- 150000002431 hydrogen Chemical group 0.000 claims description 55
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 claims description 54
- 239000010936 titanium Substances 0.000 claims description 52
- 239000011669 selenium Substances 0.000 claims description 50
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 47
- 125000000707 boryl group Chemical group B* 0.000 claims description 46
- 125000003277 amino group Chemical group 0.000 claims description 44
- 229910052711 selenium Inorganic materials 0.000 claims description 44
- 229910052717 sulfur Inorganic materials 0.000 claims description 43
- 239000000460 chlorine Substances 0.000 claims description 42
- 150000003839 salts Chemical class 0.000 claims description 42
- 229910052714 tellurium Inorganic materials 0.000 claims description 42
- 150000007944 thiolates Chemical group 0.000 claims description 42
- 150000001450 anions Chemical class 0.000 claims description 41
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 38
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 38
- 229910052698 phosphorus Inorganic materials 0.000 claims description 38
- 125000003545 alkoxy group Chemical group 0.000 claims description 37
- 229910052785 arsenic Inorganic materials 0.000 claims description 34
- 229910052787 antimony Inorganic materials 0.000 claims description 32
- 229910052797 bismuth Inorganic materials 0.000 claims description 32
- 229910052757 nitrogen Inorganic materials 0.000 claims description 32
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 claims description 30
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 claims description 28
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 27
- 239000005977 Ethylene Substances 0.000 claims description 27
- 150000001768 cations Chemical class 0.000 claims description 25
- 239000007789 gas Substances 0.000 claims description 24
- 229910052760 oxygen Inorganic materials 0.000 claims description 24
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 21
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 21
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 claims description 21
- 229920001577 copolymer Polymers 0.000 claims description 21
- 239000011574 phosphorus Substances 0.000 claims description 21
- 229910052719 titanium Inorganic materials 0.000 claims description 21
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 claims description 20
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims description 19
- 239000000155 melt Substances 0.000 claims description 19
- 229920000642 polymer Polymers 0.000 claims description 19
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 19
- 229910052723 transition metal Inorganic materials 0.000 claims description 19
- 150000003624 transition metals Chemical class 0.000 claims description 19
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 18
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 18
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 18
- 229910052799 carbon Inorganic materials 0.000 claims description 18
- 229910052732 germanium Inorganic materials 0.000 claims description 18
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 claims description 18
- 229910052710 silicon Inorganic materials 0.000 claims description 18
- 239000010703 silicon Substances 0.000 claims description 18
- 229910052718 tin Inorganic materials 0.000 claims description 18
- JLTRXTDYQLMHGR-UHFFFAOYSA-N trimethylaluminium Chemical compound C[Al](C)C JLTRXTDYQLMHGR-UHFFFAOYSA-N 0.000 claims description 18
- 239000002253 acid Substances 0.000 claims description 17
- 239000012632 extractable Substances 0.000 claims description 17
- 230000007704 transition Effects 0.000 claims description 17
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 16
- 150000008282 halocarbons Chemical class 0.000 claims description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
- 150000007513 acids Chemical class 0.000 claims description 13
- 150000004820 halides Chemical class 0.000 claims description 13
- 239000001272 nitrous oxide Substances 0.000 claims description 13
- 229910052786 argon Inorganic materials 0.000 claims description 12
- 229910052798 chalcogen Inorganic materials 0.000 claims description 12
- 229910052734 helium Inorganic materials 0.000 claims description 12
- 229910052743 krypton Inorganic materials 0.000 claims description 12
- 229910052754 neon Inorganic materials 0.000 claims description 12
- 229910052704 radon Inorganic materials 0.000 claims description 12
- 239000011593 sulfur Substances 0.000 claims description 12
- 229910052724 xenon Inorganic materials 0.000 claims description 12
- 150000001787 chalcogens Chemical class 0.000 claims description 11
- 229910052801 chlorine Inorganic materials 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 11
- 150000002902 organometallic compounds Chemical class 0.000 claims description 11
- 125000004429 atom Chemical group 0.000 claims description 9
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 claims description 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 8
- 229910052751 metal Inorganic materials 0.000 claims description 8
- 239000002184 metal Substances 0.000 claims description 8
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 claims description 8
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 7
- 238000012685 gas phase polymerization Methods 0.000 claims description 7
- 125000005843 halogen group Chemical group 0.000 claims description 7
- 230000000737 periodic effect Effects 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 150000004770 chalcogenides Chemical class 0.000 claims description 6
- 150000003949 imides Chemical class 0.000 claims description 5
- 125000002524 organometallic group Chemical group 0.000 claims description 5
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 claims description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 4
- PFRUBEOIWWEFOL-UHFFFAOYSA-N [N].[S] Chemical compound [N].[S] PFRUBEOIWWEFOL-UHFFFAOYSA-N 0.000 claims description 4
- 229910052789 astatine Inorganic materials 0.000 claims description 4
- RYXHOMYVWAEKHL-UHFFFAOYSA-N astatine atom Chemical compound [At] RYXHOMYVWAEKHL-UHFFFAOYSA-N 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 4
- 229910052794 bromium Inorganic materials 0.000 claims description 4
- 239000012530 fluid Substances 0.000 claims description 4
- 229910052731 fluorine Inorganic materials 0.000 claims description 4
- 239000011737 fluorine Substances 0.000 claims description 4
- 229910052811 halogen oxide Inorganic materials 0.000 claims description 4
- 229910000037 hydrogen sulfide Inorganic materials 0.000 claims description 4
- 229910052740 iodine Inorganic materials 0.000 claims description 4
- 239000011630 iodine Substances 0.000 claims description 4
- 150000004715 keto acids Chemical class 0.000 claims description 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 4
- JMANVNJQNLATNU-UHFFFAOYSA-N oxalonitrile Chemical compound N#CC#N JMANVNJQNLATNU-UHFFFAOYSA-N 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- 229910000061 pnictogen hydride Inorganic materials 0.000 claims description 4
- 150000003573 thiols Chemical class 0.000 claims description 4
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical group [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 150000001298 alcohols Chemical class 0.000 claims description 3
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 3
- 229910052985 chalcogen hydride Inorganic materials 0.000 claims description 3
- 150000001451 organic peroxides Chemical class 0.000 claims description 3
- 125000002577 pseudohalo group Chemical group 0.000 claims description 3
- 239000002002 slurry Substances 0.000 claims description 3
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 claims 12
- 229960001730 nitrous oxide Drugs 0.000 claims 12
- MGWGWNFMUOTEHG-UHFFFAOYSA-N 4-(3,5-dimethylphenyl)-1,3-thiazol-2-amine Chemical compound CC1=CC(C)=CC(C=2N=C(N)SC=2)=C1 MGWGWNFMUOTEHG-UHFFFAOYSA-N 0.000 claims 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 2
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 claims 2
- 125000005234 alkyl aluminium group Chemical group 0.000 claims 2
- 229910001882 dioxygen Inorganic materials 0.000 claims 2
- 229910000039 hydrogen halide Inorganic materials 0.000 claims 2
- 239000012433 hydrogen halide Substances 0.000 claims 2
- 229910017464 nitrogen compound Inorganic materials 0.000 claims 2
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 claims 2
- 235000013842 nitrous oxide Nutrition 0.000 claims 2
- 150000003623 transition metal compounds Chemical class 0.000 claims 2
- 229920000098 polyolefin Polymers 0.000 abstract description 13
- 239000011135 tin Substances 0.000 description 14
- 238000000113 differential scanning calorimetry Methods 0.000 description 13
- 239000011133 lead Substances 0.000 description 12
- 239000012071 phase Substances 0.000 description 12
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 11
- 238000004519 manufacturing process Methods 0.000 description 9
- 230000008569 process Effects 0.000 description 9
- 238000002844 melting Methods 0.000 description 8
- 230000008018 melting Effects 0.000 description 8
- 239000000178 monomer Substances 0.000 description 8
- 239000011347 resin Substances 0.000 description 8
- 229920005989 resin Polymers 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 7
- 239000002245 particle Substances 0.000 description 7
- 239000011541 reaction mixture Substances 0.000 description 7
- 230000000694 effects Effects 0.000 description 6
- 229910052749 magnesium Inorganic materials 0.000 description 6
- 239000011777 magnesium Substances 0.000 description 6
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 5
- 229920001519 homopolymer Polymers 0.000 description 5
- 230000000379 polymerizing effect Effects 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- 238000005243 fluidization Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- LFXVBWRMVZPLFK-UHFFFAOYSA-N trioctylalumane Chemical compound CCCCCCCC[Al](CCCCCCCC)CCCCCCCC LFXVBWRMVZPLFK-UHFFFAOYSA-N 0.000 description 3
- 239000004711 α-olefin Substances 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N 1-Heptene Chemical compound CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 2
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical compound CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 2
- DIKBFYAXUHHXCS-UHFFFAOYSA-N bromoform Chemical compound BrC(Br)Br DIKBFYAXUHHXCS-UHFFFAOYSA-N 0.000 description 2
- GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 239000003426 co-catalyst Substances 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 125000001188 haloalkyl group Chemical group 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- OKJPEAGHQZHRQV-UHFFFAOYSA-N iodoform Chemical compound IC(I)I OKJPEAGHQZHRQV-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000003607 modifier Substances 0.000 description 2
- 229910052756 noble gas Inorganic materials 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 125000004430 oxygen atom Chemical group O* 0.000 description 2
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
- RLOWWWKZYUNIDI-UHFFFAOYSA-N phosphinic chloride Chemical compound ClP=O RLOWWWKZYUNIDI-UHFFFAOYSA-N 0.000 description 2
- 229910052696 pnictogen Inorganic materials 0.000 description 2
- 150000003063 pnictogens Chemical class 0.000 description 2
- 229920005638 polyethylene monopolymer Polymers 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- HJUGFYREWKUQJT-UHFFFAOYSA-N tetrabromomethane Chemical compound BrC(Br)(Br)Br HJUGFYREWKUQJT-UHFFFAOYSA-N 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 229910052720 vanadium Inorganic materials 0.000 description 2
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 2
- 229910052726 zirconium Inorganic materials 0.000 description 2
- XEMRAKSQROQPBR-UHFFFAOYSA-N (trichloromethyl)benzene Chemical compound ClC(Cl)(Cl)C1=CC=CC=C1 XEMRAKSQROQPBR-UHFFFAOYSA-N 0.000 description 1
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
- ZFMWDTNZPKDVBU-UHFFFAOYSA-N 1,2,3,4-tetrachlorocyclopentane Chemical compound ClC1CC(Cl)C(Cl)C1Cl ZFMWDTNZPKDVBU-UHFFFAOYSA-N 0.000 description 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 description 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- 101100000419 Autographa californica nuclear polyhedrosis virus AC41 gene Proteins 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- 101710178035 Chorismate synthase 2 Proteins 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- 101710152694 Cysteine synthase 2 Proteins 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 101100321669 Fagopyrum esculentum FA02 gene Proteins 0.000 description 1
- 101100321670 Fagopyrum esculentum FA18 gene Proteins 0.000 description 1
- 229910005793 GeO 2 Inorganic materials 0.000 description 1
- 229910005839 GeS 2 Inorganic materials 0.000 description 1
- 239000002879 Lewis base Substances 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 1
- 241000404883 Pisa Species 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229910020346 SiS 2 Inorganic materials 0.000 description 1
- 229910006404 SnO 2 Inorganic materials 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 150000001334 alicyclic compounds Chemical class 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 150000007824 aliphatic compounds Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229940058905 antimony compound for treatment of leishmaniasis and trypanosomiasis Drugs 0.000 description 1
- 150000001463 antimony compounds Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- RDHPKYGYEGBMSE-UHFFFAOYSA-N bromoethane Chemical compound CCBr RDHPKYGYEGBMSE-UHFFFAOYSA-N 0.000 description 1
- 229950005228 bromoform Drugs 0.000 description 1
- 229910052800 carbon group element Inorganic materials 0.000 description 1
- JOHCVVJGGSABQY-UHFFFAOYSA-N carbon tetraiodide Chemical compound IC(I)(I)I JOHCVVJGGSABQY-UHFFFAOYSA-N 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000001733 carboxylic acid esters Chemical class 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- NEHMKBQYUWJMIP-NJFSPNSNSA-N chloro(114C)methane Chemical compound [14CH3]Cl NEHMKBQYUWJMIP-NJFSPNSNSA-N 0.000 description 1
- VEZNCHDBSQWUHQ-UHFFFAOYSA-N chlorocyclopropane Chemical compound ClC1CC1 VEZNCHDBSQWUHQ-UHFFFAOYSA-N 0.000 description 1
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013530 defoamer Substances 0.000 description 1
- FJBFPHVGVWTDIP-UHFFFAOYSA-N dibromomethane Chemical compound BrCBr FJBFPHVGVWTDIP-UHFFFAOYSA-N 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- YNLAOSYQHBDIKW-UHFFFAOYSA-M diethylaluminium chloride Chemical compound CC[Al](Cl)CC YNLAOSYQHBDIKW-UHFFFAOYSA-M 0.000 description 1
- NZZFYRREKKOMAT-UHFFFAOYSA-N diiodomethane Chemical compound ICI NZZFYRREKKOMAT-UHFFFAOYSA-N 0.000 description 1
- JGHYBJVUQGTEEB-UHFFFAOYSA-M dimethylalumanylium;chloride Chemical compound C[Al](C)Cl JGHYBJVUQGTEEB-UHFFFAOYSA-M 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 229940069096 dodecene Drugs 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 229960003750 ethyl chloride Drugs 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000007765 extrusion coating Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000009501 film coating Methods 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 229940093920 gynecological arsenic compound Drugs 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- CAYGQBVSOZLICD-UHFFFAOYSA-N hexabromobenzene Chemical compound BrC1=C(Br)C(Br)=C(Br)C(Br)=C1Br CAYGQBVSOZLICD-UHFFFAOYSA-N 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- ZRKSVHFXTRFQFL-UHFFFAOYSA-N isocyanomethane Chemical compound C[N+]#[C-] ZRKSVHFXTRFQFL-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000007527 lewis bases Chemical class 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229920001684 low density polyethylene Polymers 0.000 description 1
- 239000004702 low-density polyethylene Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 229940102396 methyl bromide Drugs 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- BMNDJWSIKZECMH-UHFFFAOYSA-N nitrosyl bromide Chemical compound BrN=O BMNDJWSIKZECMH-UHFFFAOYSA-N 0.000 description 1
- VPCDQGACGWYTMC-UHFFFAOYSA-N nitrosyl chloride Chemical compound ClN=O VPCDQGACGWYTMC-UHFFFAOYSA-N 0.000 description 1
- 235000019392 nitrosyl chloride Nutrition 0.000 description 1
- ZEIYBPGWHWECHV-UHFFFAOYSA-N nitrosyl fluoride Chemical compound FN=O ZEIYBPGWHWECHV-UHFFFAOYSA-N 0.000 description 1
- 150000002835 noble gases Chemical class 0.000 description 1
- 239000002667 nucleating agent Substances 0.000 description 1
- KUVXJBSVPBXHEK-UHFFFAOYSA-N octylaluminum Chemical compound CCCCCCCC[Al] KUVXJBSVPBXHEK-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 150000003961 organosilicon compounds Chemical class 0.000 description 1
- 230000001151 other effect Effects 0.000 description 1
- PDWVXNLUDMQFCH-UHFFFAOYSA-N oxoantimony;hydrochloride Chemical compound Cl.[Sb]=O PDWVXNLUDMQFCH-UHFFFAOYSA-N 0.000 description 1
- BWOROQSFKKODDR-UHFFFAOYSA-N oxobismuth;hydrochloride Chemical compound Cl.[Bi]=O BWOROQSFKKODDR-UHFFFAOYSA-N 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229910052699 polonium Inorganic materials 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000003134 recirculating effect Effects 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- RQZJHKMUYSXABM-UHFFFAOYSA-N selanylidenemethanone Chemical compound O=C=[Se] RQZJHKMUYSXABM-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000012748 slip agent Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- NNCGPRGCYAWTAF-UHFFFAOYSA-N tellurium hexafluoride Chemical compound F[Te](F)(F)(F)(F)F NNCGPRGCYAWTAF-UHFFFAOYSA-N 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 1
- ORYGRKHDLWYTKX-UHFFFAOYSA-N trihexylalumane Chemical compound CCCCCC[Al](CCCCCC)CCCCCC ORYGRKHDLWYTKX-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- 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
- C08F2/00—Processes of polymerisation
- C08F2/12—Polymerisation in non-solvents
- C08F2/16—Aqueous medium
- C08F2/18—Suspension polymerisation
-
- 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
- C08F2/00—Processes of polymerisation
- C08F2/34—Polymerisation in gaseous state
-
- 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
- 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
- C08F4/602—Component covered by group C08F4/60 with an organo-aluminium 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
- C08F4/607—Catalysts containing a specific non-metal or metal-free compound
- C08F4/609—Catalysts containing a specific non-metal or metal-free compound organic
- C08F4/6093—Catalysts containing a specific non-metal or metal-free compound organic containing halogen
-
- 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
- C08F4/607—Catalysts containing a specific non-metal or metal-free compound
- C08F4/609—Catalysts containing a specific non-metal or metal-free compound organic
- C08F4/6094—Catalysts containing a specific non-metal or metal-free compound organic containing oxygen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Emergency Medicine (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Polymerisation Methods In General (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10578698P | 1998-10-27 | 1998-10-27 | |
| US60/105,786 | 1998-10-27 | ||
| US38654799A | 1999-08-31 | 1999-08-31 | |
| US09/386,547 | 1999-08-31 | ||
| PCT/US1999/024240 WO2000024790A2 (en) | 1998-10-27 | 1999-10-14 | Process for the polymerization of olefins; polyethylenes, a nd films and articles produced therefrom |
Related Child Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010224210A Division JP2011026612A (ja) | 1998-10-27 | 2010-10-01 | オレフィンの重合方法、新規ポリエチレン並びにそれから製造されるフィルム及び物品 |
| JP2012205791A Division JP5685233B2 (ja) | 1998-10-27 | 2012-09-19 | エチレンとオレフィンとのコポリマー並びにそれから製造されるフィルム及び物品 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2002528575A true JP2002528575A (ja) | 2002-09-03 |
| JP2002528575A5 JP2002528575A5 (enExample) | 2006-11-30 |
Family
ID=26802940
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000578359A Withdrawn JP2002528575A (ja) | 1998-10-27 | 1999-10-14 | オレフィンの重合方法、新規ポリエチレン並びにそれから製造されるフィルム及び物品 |
| JP2010224210A Pending JP2011026612A (ja) | 1998-10-27 | 2010-10-01 | オレフィンの重合方法、新規ポリエチレン並びにそれから製造されるフィルム及び物品 |
| JP2012205791A Expired - Lifetime JP5685233B2 (ja) | 1998-10-27 | 2012-09-19 | エチレンとオレフィンとのコポリマー並びにそれから製造されるフィルム及び物品 |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010224210A Pending JP2011026612A (ja) | 1998-10-27 | 2010-10-01 | オレフィンの重合方法、新規ポリエチレン並びにそれから製造されるフィルム及び物品 |
| JP2012205791A Expired - Lifetime JP5685233B2 (ja) | 1998-10-27 | 2012-09-19 | エチレンとオレフィンとのコポリマー並びにそれから製造されるフィルム及び物品 |
Country Status (10)
| Country | Link |
|---|---|
| US (3) | US6608152B2 (enExample) |
| EP (10) | EP1047717B2 (enExample) |
| JP (3) | JP2002528575A (enExample) |
| KR (1) | KR100610968B1 (enExample) |
| CN (2) | CN101012296B (enExample) |
| AT (6) | ATE544789T1 (enExample) |
| BR (1) | BR9907069A (enExample) |
| CA (1) | CA2314140A1 (enExample) |
| DE (3) | DE69943137D1 (enExample) |
| WO (1) | WO2000024790A2 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2003508557A (ja) * | 1999-08-31 | 2003-03-04 | イーストマン ケミカル カンパニー | ポリオレフィンの製造方法 |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1047717B2 (en) * | 1998-10-27 | 2022-10-19 | Eastman Chemical Company | Process for the polymerization of olefins; polyethylenes, and films and articles produced therefrom |
| CA2381913A1 (en) | 1999-08-31 | 2001-03-08 | Eastman Chemical Company | Process for producing polyolefins |
| US6191238B1 (en) * | 1999-08-31 | 2001-02-20 | Eastman Chemical Company | Process for producing polyolefins |
| JP2001342213A (ja) * | 2000-03-30 | 2001-12-11 | Sumitomo Chem Co Ltd | 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 |
| US6951804B2 (en) * | 2001-02-02 | 2005-10-04 | Applied Materials, Inc. | Formation of a tantalum-nitride layer |
| US7378476B2 (en) * | 2004-06-25 | 2008-05-27 | Ineos Usa Llc | Olefin polymerization process in the presence of a radical generating system |
| US7789117B2 (en) * | 2006-01-27 | 2010-09-07 | The Goodyear Tire & Rubber Company | Tire with circumferential rubber tread having a lateral outboard control element |
| US10053574B2 (en) | 2014-08-15 | 2018-08-21 | Westlake Longview Corporation | Maleic anhydride grafted LLDPE having high melt index |
| CA2969627C (en) | 2017-05-30 | 2024-01-16 | Nova Chemicals Corporation | Ethylene copolymer having enhanced film properties |
| JP6852653B2 (ja) | 2017-11-07 | 2021-03-31 | トヨタ自動車株式会社 | 正極活物質およびフッ化物イオン電池 |
| CN111072797B (zh) * | 2018-10-19 | 2021-07-02 | 中国石油化工股份有限公司 | 烯烃聚合催化剂球形载体及其制备方法和催化剂组分与催化剂及应用 |
| CN115254151B (zh) * | 2022-08-18 | 2023-06-16 | 陕西科技大学 | 一种核壳结构BiVO4@BiOCl异质结及其制备方法和应用 |
| WO2025217072A1 (en) | 2024-04-07 | 2025-10-16 | Formosa Plastics Corporation, Usa | High dart impact and tear films from titanium based prepolymer catalyzed polyethylenes |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS56106910A (en) * | 1978-11-20 | 1981-08-25 | Union Carbide Corp | Manufacture of low density ethylene copolymer in fluidized bed reactor |
| JPH02214703A (ja) * | 1988-12-22 | 1990-08-27 | Bp Chem Internatl Ltd | 活性剤と活性遅延剤とを重合媒体へ同時に添加することにより制御されるα―オレフィンの気相重合方法 |
| JPH02219806A (ja) * | 1988-12-14 | 1990-09-03 | Soc Atochem | 分子量分布の狭い直鎖状ポリエチレンを製造しうるエチレンの気相重合方法 |
| JPH0532718A (ja) * | 1991-01-26 | 1993-02-09 | Basf Ag | ツイーグラー触媒系のためのバナジウムおよびマグネシウム含有組成分 |
| JPH05194646A (ja) * | 1991-08-30 | 1993-08-03 | Bp Chem Internatl Ltd | エチレン重合方法 |
| JPH06199915A (ja) * | 1992-12-31 | 1994-07-19 | Nippon Petrochem Co Ltd | ポリオレフィンの製造方法 |
| JPH08134124A (ja) * | 1994-10-25 | 1996-05-28 | Bp Chem Internatl Ltd | チーグラー・ナッタ触媒によるオレフィンの重合方法 |
| JP2002528574A (ja) * | 1998-10-27 | 2002-09-03 | イーストマン ケミカル カンパニー | オレフィンの重合方法 |
Family Cites Families (95)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US33683A (en) | 1861-11-05 | Improved steering apparatus | ||
| DE1016022B (de) | 1954-01-19 | 1957-09-19 | Dr Dr E H Karl Ziegler | Verfahren zur Herstellung von hochmolekularen Polyaethylenen |
| BE559727A (enExample) | 1956-08-02 | |||
| US3163611A (en) * | 1957-11-07 | 1964-12-29 | Monsanto Co | Method of preparing a modified ziegler polymerization catalyst |
| US2996459A (en) * | 1958-02-03 | 1961-08-15 | Monsanto Chemicals | Method for preparing a ziegler polymerization catalyst |
| US3184416A (en) * | 1958-05-22 | 1965-05-18 | Monsanto Co | Production of ziegler polymerization catalysts |
| US3440237A (en) * | 1958-05-22 | 1969-04-22 | Monsanto Co | Production of polyethylene with water-modified ziegler catalyst |
| CH392891A (de) * | 1959-03-04 | 1965-05-31 | Dynamit Nobel Ag | Verfahren zum Polymerisieren von Monoolefinen zu hochmolekularen kunststoffartigen Polymerisaten unter Verwendung eines Dreikomponentenkatalysators |
| BE614201A (enExample) * | 1961-02-23 | |||
| DE1720262C3 (de) * | 1967-02-11 | 1981-11-26 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Polymerisation von α-Olefinen |
| US3639375A (en) * | 1967-02-11 | 1972-02-01 | Basf Ag | Production of alpha-olefin polymers |
| FR1550186A (enExample) | 1967-08-31 | 1968-12-20 | ||
| DE1720315C3 (de) * | 1967-10-13 | 1980-02-07 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Polymerisation von a -Olefinen mit 2 bis 8 Kohlenstoffatomen |
| FR2001271A1 (enExample) * | 1968-02-08 | 1969-09-26 | Sumitomo Chemical Co | |
| US3676415A (en) | 1968-06-27 | 1972-07-11 | Hoechst Ag | Process for polymerizing {60 -olefins |
| US3644318A (en) | 1968-08-21 | 1972-02-22 | Hoechst Ag | Process for the polymerization of olefins |
| US4003712A (en) | 1970-07-29 | 1977-01-18 | Union Carbide Corporation | Fluidized bed reactor |
| NO136797C (no) | 1970-09-25 | 1977-11-09 | Union Carbide Corp | Fremgangsm}te for polymerisering av etylen med modifisert katalysator |
| US4012573A (en) | 1970-10-09 | 1977-03-15 | Basf Aktiengesellschaft | Method of removing heat from polymerization reactions of monomers in the gas phase |
| JPS497075B1 (enExample) * | 1970-12-29 | 1974-02-18 | ||
| US3709853A (en) | 1971-04-29 | 1973-01-09 | Union Carbide Corp | Polymerization of ethylene using supported bis-(cyclopentadienyl)chromium(ii)catalysts |
| JPS497075A (enExample) | 1972-05-08 | 1974-01-22 | ||
| LU65587A1 (enExample) | 1972-06-22 | 1973-12-27 | ||
| GB1419772A (en) * | 1972-07-20 | 1975-12-31 | Ici Ltd | Olefine polymerisation catalysts and process of polymerising olefines |
| US3917575A (en) | 1972-11-11 | 1975-11-04 | Nippon Oil Co Ltd | Process for production of polyolefins |
| DE2301136C3 (de) * | 1973-01-11 | 1980-08-28 | Basf Ag, 6700 Ludwigshafen | Verfahren zum Herstellen einer modifizierten Titan-Komponente fur Katalysatoren des Ziegler-Natta-Typs |
| JPS5133211B2 (enExample) | 1974-02-04 | 1976-09-18 | ||
| DE2406900A1 (de) * | 1974-02-14 | 1975-08-28 | Basf Ag | Verfahren zur herstellung von homopolymerisaten des 4-methylpenten- |
| US3992320A (en) * | 1974-08-24 | 1976-11-16 | Basf Aktiengesellschaft | Manufacture of a modified titanium component for catalysts of the Ziegler-Natta type |
| DE2441541C2 (de) * | 1974-08-30 | 1982-07-15 | Basf Ag, 6700 Ludwigshafen | Verfahren zum Herstellen einer modifizierten Titan-Komponente für Katalysatoren des Ziegler-Natta-Typs |
| US4105847A (en) | 1974-11-26 | 1978-08-08 | Mitsui Toatsu Chemicals Inc. | Method for polymerization of ethylene |
| US4011382A (en) | 1975-03-10 | 1977-03-08 | Union Carbide Corporation | Preparation of low and medium density ethylene polymer in fluid bed reactor |
| DE2553179A1 (de) | 1975-11-27 | 1977-06-08 | Hoechst Ag | Verfahren zur herstellung eines katalysators |
| JPS607645B2 (ja) * | 1976-04-19 | 1985-02-26 | チッソ株式会社 | 共重合体ポリプロピレン用触媒の重合前活性化による該共重合体の製造法 |
| GR63148B (en) | 1976-05-17 | 1979-09-25 | Mitsui Toatsu Chemicals | Process for the polymerization of ethylene of a-olefins and catalyst therefor |
| US4256866A (en) | 1976-06-16 | 1981-03-17 | Standard Oil Company (Indiana) | Polymerization process |
| DE2801541A1 (de) | 1978-01-14 | 1979-07-19 | Hoechst Ag | Aethylencopolymere und ihre verwendung zur herstellung von folien |
| US4302566A (en) | 1978-03-31 | 1981-11-24 | Union Carbide Corporation | Preparation of ethylene copolymers in fluid bed reactor |
| US4302565A (en) | 1978-03-31 | 1981-11-24 | Union Carbide Corporation | Impregnated polymerization catalyst, process for preparing, and use for ethylene copolymerization |
| DE2837481C2 (de) * | 1978-08-28 | 1983-08-04 | Ruhrchemie Ag, 4200 Oberhausen | Verfahren zur Herstellung von Polymerisaten des Ethylens |
| JPS603324B2 (ja) | 1978-12-28 | 1985-01-28 | 三井化学株式会社 | エチレン共重合体の製造方法 |
| US4293673A (en) | 1978-12-28 | 1981-10-06 | Union Carbide Corporation | Spheroidal polymerization catalyst, process for preparing, and use for ethylene polymerization |
| US4211670A (en) * | 1979-01-25 | 1980-07-08 | Hercules Incorporated | Titanium trichloride catalyst component for propylene polymerization |
| US4363904A (en) | 1979-06-18 | 1982-12-14 | Union Carbide Corporation | High tear strength polymers |
| US4482687A (en) | 1979-10-26 | 1984-11-13 | Union Carbide Corporation | Preparation of low-density ethylene copolymers in fluid bed reactor |
| US4331789A (en) * | 1980-03-14 | 1982-05-25 | Phillips Petroleum Company | Polymerization using a selenium or tellurium treated catalyst |
| DE3021296A1 (de) * | 1980-06-06 | 1982-01-07 | Basf Ag, 6700 Ludwigshafen | Verfahren zum herstellen einer titan-iii-komponente fuer ziegler-natta-katalysatorsysteme |
| US4597920A (en) | 1981-04-23 | 1986-07-01 | E. I. Du Pont De Nemours And Company | Shrink films of ethylene/α-olefin copolymers |
| US4481301A (en) | 1981-12-04 | 1984-11-06 | Mobil Oil Corporation | Highly active catalyst composition for polymerizing alpha-olefins |
| US4543399A (en) | 1982-03-24 | 1985-09-24 | Union Carbide Corporation | Fluidized bed reaction systems |
| IT1178466B (it) * | 1984-03-20 | 1987-09-09 | Montedison Spa | Catalizzatori per la omo e copolimerizzazione dell'etilene e polimeri ottenuti |
| CA1340037C (en) * | 1985-06-17 | 1998-09-08 | Stanley Lustig | Puncture resistant, heat-shrinkable films containing very low density polyethylene copolymer |
| US5191052A (en) | 1985-06-21 | 1993-03-02 | Exxon Chemical Patents Inc. | Copolymers of ethylene and 1,3-butadiene |
| USRE33683E (en) | 1986-01-24 | 1991-09-03 | Mobil Oil Corporation | Catalyst composition for polymerizing alpha-olefins |
| US4659685A (en) | 1986-03-17 | 1987-04-21 | The Dow Chemical Company | Heterogeneous organometallic catalysts containing a supported titanium compound and at least one other supported organometallic compound |
| NZ220764A (en) * | 1986-07-02 | 1989-09-27 | Shionogi & Co | Crystalline form of 7beta((z)-2-(2-aminothiazol-4-yl)-4- carboxybut-2-enoylamino)-3-cephem-4-carboxylic acid and pharmaceutical compositions |
| FR2618786B1 (fr) | 1987-07-31 | 1989-12-01 | Bp Chimie Sa | Procede de polymerisation d'olefines en phase gazeuse dans un reacteur a lit fluidise |
| US5075271A (en) * | 1988-01-15 | 1991-12-24 | Mobil Oil Corporation | Olefin polymerization process for preparing high density or linear low density polymers of controlled molecular weight distribution |
| FI81004C (fi) | 1988-02-25 | 1990-09-10 | Suomen Sokeri Oy | Binde- och utspaedningsmedel pao basis av xylitol och foerfarande foer dess framstaellning. |
| FR2646426B2 (fr) | 1988-09-13 | 1991-08-16 | Bp Chemicals Sa | Procede et appareillage de polymerisation d'alpha-olefine en phase gazeuse en presence d'un agent ralentisseur d'activite |
| CA2003882C (en) * | 1988-12-19 | 1997-01-07 | Edwin Rogers Smith | Heat shrinkable very low density polyethylene terpolymer film |
| US5244987A (en) | 1988-12-22 | 1993-09-14 | Bf Chemicals Limited | Process for alpha-olefin gas-phase polymerization controlled by the simultaneous addition of an activator and an activity retarder to the polymerization medium |
| US6025448A (en) | 1989-08-31 | 2000-02-15 | The Dow Chemical Company | Gas phase polymerization of olefins |
| US5296430A (en) * | 1989-09-20 | 1994-03-22 | Idemitsu Petrochemical Company, Ltd. | Method for the preparation of a stabilized catalyst for the polymerization of olefins |
| FR2656315B1 (fr) | 1989-12-22 | 1992-04-17 | Bp Chemicals Snc | Procede de preparation d'un catalyseur a base de zirconium supporte sur du chlorure de magnesium, et utilisation du catalyseur dans la polymerisation des olefines. |
| CA2032543A1 (en) † | 1989-12-26 | 1991-06-27 | Robert Olds Hagerty | Dimethylaluminum chloride-activated olefin polymerisation catalyst composition |
| CA2033001C (en) | 1989-12-26 | 2003-04-08 | Robert Olds Hagerty | Catalyst composition for polymerizing olefins to polymers having good compositional homogeneity |
| US5118757A (en) * | 1990-03-26 | 1992-06-02 | Shell Oil Company | Polymer production |
| US5258475A (en) | 1991-07-12 | 1993-11-02 | Mobil Oil Corporation | Catalyst systems for polymerization and copolymerization of olefins |
| US5139986A (en) † | 1991-08-06 | 1992-08-18 | Mobil Oil Corporation | Catalyst composition for production of linear low-density ethylene-hexene copolymers and films thereof |
| US5470812A (en) | 1991-11-06 | 1995-11-28 | Mobil Oil Corporation | High activity polyethylene catalysts prepared with alkoxysilane reagents |
| IT1262933B (it) | 1992-01-31 | 1996-07-22 | Montecatini Tecnologie Srl | Processo per la polimerizzazione in fase gas di alfa-olefine |
| US5352749A (en) | 1992-03-19 | 1994-10-04 | Exxon Chemical Patents, Inc. | Process for polymerizing monomers in fluidized beds |
| US5283128A (en) | 1992-03-23 | 1994-02-01 | Viskase Corporation | Biaxially oriented heat shrinkable film |
| US6143854A (en) * | 1993-08-06 | 2000-11-07 | Exxon Chemical Patents, Inc. | Polymerization catalysts, their production and use |
| US5308818A (en) * | 1992-06-08 | 1994-05-03 | Fina Technology, Inc. | Catalyst system for the polymerization of olefins |
| JP3222596B2 (ja) | 1992-12-29 | 2001-10-29 | 日本石油化学株式会社 | α−オレフィンの重合開始方法 |
| ZA943399B (en) | 1993-05-20 | 1995-11-17 | Bp Chem Int Ltd | Polymerisation process |
| FR2707651B1 (fr) | 1993-07-13 | 1995-08-25 | Bp Chemicals Snc | Procédé pour augmenter l'activité d'un catalyseur de type Ziegler-Natta. |
| WO1995002630A1 (en) | 1993-07-16 | 1995-01-26 | Exxon Chemical Patents Inc. | Polymeric films with low water vapor transmission rates |
| DE69422410T2 (de) | 1993-08-06 | 2000-07-06 | Exxon Chemical Patents, Inc. | Polymerisationskataylsatoren, ihre herstellung und verwendung |
| IT1273661B (it) * | 1994-07-20 | 1997-07-09 | Spherilene Srl | Catalizzatori per la polimerizzazione delle olefine |
| US5600353A (en) * | 1995-03-01 | 1997-02-04 | Hewlett-Packard Company | Method of transitioning between ink jet printing modes |
| US6191246B1 (en) * | 1995-05-31 | 2001-02-20 | Sasol Technology (Proprietary) Limited | Ethylene-pentene-hexene copolymer, process for its preparation and use for the production of films |
| US6248380B1 (en) | 1995-06-06 | 2001-06-19 | Cryovac, Inc. | Package having a dual-film lid comprising a gas-impermeable film and a delaminatable, gas-permeable film |
| RU2135520C1 (ru) | 1995-09-25 | 1999-08-27 | Юнион Карбайд Кемикалз Энд Пластикс Текнолоджи Корпорейшн | Способ газофазной полимеризации |
| FI104825B (fi) * | 1996-01-26 | 2000-04-14 | Borealis As | Olefiinien polymerointikatalysaattorisysteemi, sen valmistus ja käyttö |
| US5837064A (en) * | 1996-10-04 | 1998-11-17 | Eco-Snow Systems, Inc. | Electrostatic discharge protection of static sensitive devices cleaned with carbon dioxide spray |
| US6329476B1 (en) | 1997-10-14 | 2001-12-11 | Phillips Petroleum Company | Olefin polymerization processes and products thereof |
| WO1999020663A2 (en) * | 1997-10-17 | 1999-04-29 | Exxon Chemical Patents Inc. | High impact, flexural moduli polymeric materials formed using sequential donors |
| EP1047717B2 (en) | 1998-10-27 | 2022-10-19 | Eastman Chemical Company | Process for the polymerization of olefins; polyethylenes, and films and articles produced therefrom |
| US6133378A (en) | 1998-11-20 | 2000-10-17 | Bridgestone/Firestone, Inc. | EPDM-based roofing shingle compositions |
| US6417301B1 (en) | 1999-06-07 | 2002-07-09 | Eastman Chemical Company | Process for producing ethylene/olefin interpolymers |
| TW553955B (en) * | 1999-09-06 | 2003-09-21 | Sumitomo Chemical Co | A method for producing poly(p-t-butoxystyrene) |
| BRPI0720422B1 (pt) | 2006-12-18 | 2018-02-14 | Univation Technologies, Llc | Método para controlar uma transição de uma reação de polimerização inicial para uma reação de polimerização alvo em um reator de leito fluidizado |
-
1999
- 1999-10-14 EP EP99954979.3A patent/EP1047717B2/en not_active Expired - Lifetime
- 1999-10-14 EP EP10010550A patent/EP2277922A1/en not_active Withdrawn
- 1999-10-14 EP EP10010560A patent/EP2275455A1/en not_active Withdrawn
- 1999-10-14 EP EP05000815A patent/EP1522544B1/en not_active Expired - Lifetime
- 1999-10-14 DE DE69943137T patent/DE69943137D1/de not_active Expired - Lifetime
- 1999-10-14 EP EP07008240A patent/EP1860127B1/en not_active Expired - Lifetime
- 1999-10-14 CN CN2007100067069A patent/CN101012296B/zh not_active Expired - Lifetime
- 1999-10-14 CN CNB998033669A patent/CN1307211C/zh not_active Expired - Lifetime
- 1999-10-14 CA CA002314140A patent/CA2314140A1/en not_active Abandoned
- 1999-10-14 AT AT10010561T patent/ATE544789T1/de active
- 1999-10-14 AT AT07008240T patent/ATE495202T1/de not_active IP Right Cessation
- 1999-10-14 EP EP10010552A patent/EP2277924B1/en not_active Expired - Lifetime
- 1999-10-14 BR BR9907069-3A patent/BR9907069A/pt not_active IP Right Cessation
- 1999-10-14 EP EP10010551A patent/EP2277923B1/en not_active Expired - Lifetime
- 1999-10-14 EP EP10010561A patent/EP2287211B1/en not_active Expired - Lifetime
- 1999-10-14 DE DE69924965.1T patent/DE69924965T3/de not_active Expired - Lifetime
- 1999-10-14 DE DE69938367T patent/DE69938367T2/de not_active Expired - Lifetime
- 1999-10-14 KR KR1020007007147A patent/KR100610968B1/ko not_active Expired - Lifetime
- 1999-10-14 AT AT05000815T patent/ATE388967T1/de not_active IP Right Cessation
- 1999-10-14 AT AT10010562T patent/ATE528327T1/de not_active IP Right Cessation
- 1999-10-14 AT AT10010551T patent/ATE528328T1/de not_active IP Right Cessation
- 1999-10-14 AT AT99954979T patent/ATE294194T1/de not_active IP Right Cessation
- 1999-10-14 WO PCT/US1999/024240 patent/WO2000024790A2/en not_active Ceased
- 1999-10-14 EP EP10010562A patent/EP2275456B1/en not_active Expired - Lifetime
- 1999-10-14 JP JP2000578359A patent/JP2002528575A/ja not_active Withdrawn
- 1999-10-14 EP EP10010553A patent/EP2277925A1/en not_active Withdrawn
-
2001
- 2001-07-27 US US09/917,307 patent/US6608152B2/en not_active Expired - Lifetime
-
2003
- 2003-06-19 US US10/465,194 patent/US7652113B2/en not_active Expired - Lifetime
-
2007
- 2007-08-20 US US11/841,666 patent/US7893180B2/en not_active Expired - Fee Related
-
2010
- 2010-10-01 JP JP2010224210A patent/JP2011026612A/ja active Pending
-
2012
- 2012-09-19 JP JP2012205791A patent/JP5685233B2/ja not_active Expired - Lifetime
Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS56106910A (en) * | 1978-11-20 | 1981-08-25 | Union Carbide Corp | Manufacture of low density ethylene copolymer in fluidized bed reactor |
| JPH02219806A (ja) * | 1988-12-14 | 1990-09-03 | Soc Atochem | 分子量分布の狭い直鎖状ポリエチレンを製造しうるエチレンの気相重合方法 |
| JPH02214703A (ja) * | 1988-12-22 | 1990-08-27 | Bp Chem Internatl Ltd | 活性剤と活性遅延剤とを重合媒体へ同時に添加することにより制御されるα―オレフィンの気相重合方法 |
| JPH0532718A (ja) * | 1991-01-26 | 1993-02-09 | Basf Ag | ツイーグラー触媒系のためのバナジウムおよびマグネシウム含有組成分 |
| JPH05194646A (ja) * | 1991-08-30 | 1993-08-03 | Bp Chem Internatl Ltd | エチレン重合方法 |
| JPH06199915A (ja) * | 1992-12-31 | 1994-07-19 | Nippon Petrochem Co Ltd | ポリオレフィンの製造方法 |
| JPH08134124A (ja) * | 1994-10-25 | 1996-05-28 | Bp Chem Internatl Ltd | チーグラー・ナッタ触媒によるオレフィンの重合方法 |
| JP2002528574A (ja) * | 1998-10-27 | 2002-09-03 | イーストマン ケミカル カンパニー | オレフィンの重合方法 |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2003508557A (ja) * | 1999-08-31 | 2003-03-04 | イーストマン ケミカル カンパニー | ポリオレフィンの製造方法 |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5685233B2 (ja) | エチレンとオレフィンとのコポリマー並びにそれから製造されるフィルム及び物品 | |
| US20020004566A1 (en) | Process for the polymerization of olefins; novel polyolefins, and films and articles produced therefrom | |
| JP4261064B2 (ja) | オレフィンの重合方法 | |
| MXPA00006282A (en) | Process for the polymerization of olefins;polyethylenes, and films and articles produced therefrom | |
| CZ20002404A3 (cs) | Způsob polymerace olefinů, nové polyethyleny a film a výrobky z nich vyrobené |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20061010 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20061010 |
|
| A711 | Notification of change in applicant |
Free format text: JAPANESE INTERMEDIATE CODE: A711 Effective date: 20070703 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20091026 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20091110 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20100205 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20100215 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20100601 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20101001 |
|
| A911 | Transfer to examiner for re-examination before appeal (zenchi) |
Free format text: JAPANESE INTERMEDIATE CODE: A911 Effective date: 20101012 |
|
| A912 | Re-examination (zenchi) completed and case transferred to appeal board |
Free format text: JAPANESE INTERMEDIATE CODE: A912 Effective date: 20101105 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20111212 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20111216 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20120919 |
|
| A761 | Written withdrawal of application |
Free format text: JAPANESE INTERMEDIATE CODE: A761 Effective date: 20121011 |