NO309380B1 - Katalysatorbestanddel og katalysatorer for polymerisering av olefiner, samt fremgangsmåte for polymerisering av olefiner - Google Patents

Katalysatorbestanddel og katalysatorer for polymerisering av olefiner, samt fremgangsmåte for polymerisering av olefiner Download PDF

Info

Publication number: NO309380B1
Authority: NO; Norway
Prior art keywords: bis; methoxymethyl; radicals; equal; carbon atoms
Prior art date: 1995-02-21

Application number

NO960669A

Other languages

English (en)

Norwegian (no)

Other versions

NO960669D0 (no

NO960669L (no

Inventor

Giampiero Morini

Enrico Albizzati

Giulio Balbontin

Giovanni Baruzzi

Antonio Cristofori

Original Assignee

Montell North America Inc

Priority date (The priority date 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 date listed.)

1995-02-21

Filing date

1996-02-20

Publication date

2001-01-22

1995-02-21 Priority claimed from IT95MI000318 external-priority patent/IT1274252B/it

1995-02-21 Priority claimed from ITMI950317 external-priority patent/IT1274251B/it

1996-02-20 Application filed by Montell North America Inc filed Critical Montell North America Inc

1996-02-20 Publication of NO960669D0 publication Critical patent/NO960669D0/no

1996-08-22 Publication of NO960669L publication Critical patent/NO960669L/no

2001-01-22 Publication of NO309380B1 publication Critical patent/NO309380B1/no

Links

239000003054 catalyst Substances 0.000 title claims description 89
238000006116 polymerization reaction Methods 0.000 title claims description 29
150000001336 alkenes Chemical class 0.000 title claims description 26
238000000034 method Methods 0.000 title claims description 17
-1 magnesium halide Chemical class 0.000 claims description 147
150000001875 compounds Chemical class 0.000 claims description 58
239000011949 solid catalyst Substances 0.000 claims description 53
125000004432 carbon atom Chemical group C* 0.000 claims description 48
150000003254 radicals Chemical class 0.000 claims description 43
125000004122 cyclic group Chemical group 0.000 claims description 38
229910052736 halogen Inorganic materials 0.000 claims description 28
XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 claims description 27
229910052739 hydrogen Inorganic materials 0.000 claims description 26
239000001257 hydrogen Substances 0.000 claims description 26
229910003074 TiCl4 Inorganic materials 0.000 claims description 25
125000001424 substituent group Chemical group 0.000 claims description 25
150000002367 halogens Chemical class 0.000 claims description 24
TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 claims description 23
229910052757 nitrogen Inorganic materials 0.000 claims description 23
238000006243 chemical reaction Methods 0.000 claims description 22
125000004433 nitrogen atom Chemical group N* 0.000 claims description 22
125000005842 heteroatom Chemical group 0.000 claims description 21
229910052799 carbon Inorganic materials 0.000 claims description 20
125000003710 aryl alkyl group Chemical group 0.000 claims description 19
125000003118 aryl group Chemical group 0.000 claims description 19
239000011777 magnesium Substances 0.000 claims description 19
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 18
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 18
229910052717 sulfur Inorganic materials 0.000 claims description 18
229910052710 silicon Inorganic materials 0.000 claims description 17
125000000753 cycloalkyl group Chemical group 0.000 claims description 16
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 16
229910052749 magnesium Inorganic materials 0.000 claims description 16
229910052760 oxygen Inorganic materials 0.000 claims description 16
239000000460 chlorine Substances 0.000 claims description 15
229910052801 chlorine Inorganic materials 0.000 claims description 15
229910052731 fluorine Inorganic materials 0.000 claims description 15
239000010936 titanium Substances 0.000 claims description 14
125000000217 alkyl group Chemical group 0.000 claims description 13
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 12
239000007787 solid Substances 0.000 claims description 12
150000003609 titanium compounds Chemical class 0.000 claims description 11
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 10
239000004215 Carbon black (E152) Substances 0.000 claims description 10
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 10
229930195733 hydrocarbon Natural products 0.000 claims description 10
239000000203 mixture Substances 0.000 claims description 10
150000001721 carbon Chemical group 0.000 claims description 9
239000002904 solvent Substances 0.000 claims description 9
ZWINORFLMHROGF-UHFFFAOYSA-N 9,9-bis(methoxymethyl)fluorene Chemical compound C1=CC=C2C(COC)(COC)C3=CC=CC=C3C2=C1 ZWINORFLMHROGF-UHFFFAOYSA-N 0.000 claims description 8
239000007789 gas Substances 0.000 claims description 8
239000012071 phase Substances 0.000 claims description 8
125000006651 (C3-C20) cycloalkyl group Chemical group 0.000 claims description 7
150000004820 halides Chemical class 0.000 claims description 7
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 6
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 6
239000007791 liquid phase Substances 0.000 claims description 6
239000001301 oxygen Substances 0.000 claims description 6
229910052698 phosphorus Inorganic materials 0.000 claims description 6
229920006395 saturated elastomer Polymers 0.000 claims description 6
150000005840 aryl radicals Chemical group 0.000 claims description 5
150000002431 hydrogen Chemical class 0.000 claims description 5
125000003367 polycyclic group Chemical group 0.000 claims description 5
125000004434 sulfur atom Chemical group 0.000 claims description 5
RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidine Chemical group CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 claims description 4
150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 4
125000001033 ether group Chemical group 0.000 claims description 4
125000004430 oxygen atom Chemical group O* 0.000 claims description 4
OTIJMHPVYPMCPU-UHFFFAOYSA-N 1,1-bis(methoxymethyl)-2,3-dimethylindene Chemical compound C1=CC=C2C(COC)(COC)C(C)=C(C)C2=C1 OTIJMHPVYPMCPU-UHFFFAOYSA-N 0.000 claims description 3
HHGPZISECHQRLO-UHFFFAOYSA-N 1,1-bis(methoxymethyl)-2-methyl-4-phenylindene Chemical compound COCC1(COC)C(C)=CC2=C1C=CC=C2C1=CC=CC=C1 HHGPZISECHQRLO-UHFFFAOYSA-N 0.000 claims description 3
FXWFWIIEIAUQHQ-UHFFFAOYSA-N 1,1-bis(methoxymethyl)-2-phenylindene Chemical compound C=1C2=CC=CC=C2C(COC)(COC)C=1C1=CC=CC=C1 FXWFWIIEIAUQHQ-UHFFFAOYSA-N 0.000 claims description 3
ZZPVNMUQOQQUHU-UHFFFAOYSA-N 1,1-bis(methoxymethyl)-4,7-dimethylindene Chemical compound CC1=CC=C(C)C2=C1C(COC)(COC)C=C2 ZZPVNMUQOQQUHU-UHFFFAOYSA-N 0.000 claims description 3
JEENAIJBWUBGSW-UHFFFAOYSA-N 1,1-bis(methoxymethyl)-7-(3,3,3-trifluoropropyl)indene Chemical compound C1=CC(CCC(F)(F)F)=C2C(COC)(COC)C=CC2=C1 JEENAIJBWUBGSW-UHFFFAOYSA-N 0.000 claims description 3
ZOIKOBDBSUJRNE-UHFFFAOYSA-N 1,1-bis(methoxymethyl)-7-methylindene Chemical compound C1=CC(C)=C2C(COC)(COC)C=CC2=C1 ZOIKOBDBSUJRNE-UHFFFAOYSA-N 0.000 claims description 3
UQGOQZUZKNXSTQ-UHFFFAOYSA-N 1,1-bis(methoxymethyl)-7-phenylindene Chemical compound C=12C(COC)(COC)C=CC2=CC=CC=1C1=CC=CC=C1 UQGOQZUZKNXSTQ-UHFFFAOYSA-N 0.000 claims description 3
VJTYHGPEEHLNGJ-UHFFFAOYSA-N 1,1-bis(methoxymethyl)-7-propan-2-ylindene Chemical compound C1=CC(C(C)C)=C2C(COC)(COC)C=CC2=C1 VJTYHGPEEHLNGJ-UHFFFAOYSA-N 0.000 claims description 3
ILXXAZBXJLMEQM-UHFFFAOYSA-N 1,1-bis(methoxymethyl)indene Chemical compound C1=CC=C2C(COC)(COC)C=CC2=C1 ILXXAZBXJLMEQM-UHFFFAOYSA-N 0.000 claims description 3
SCTKUNIIBPPKNV-UHFFFAOYSA-N 1,8-dichloro-9,9-bis(methoxymethyl)fluorene Chemical compound C12=CC=CC(Cl)=C2C(COC)(COC)C2=C1C=CC=C2Cl SCTKUNIIBPPKNV-UHFFFAOYSA-N 0.000 claims description 3
PEKQXDFNLCXEIG-UHFFFAOYSA-N 1,8-difluoro-9,9-bis(methoxymethyl)fluorene Chemical compound C12=CC=CC(F)=C2C(COC)(COC)C2=C1C=CC=C2F PEKQXDFNLCXEIG-UHFFFAOYSA-N 0.000 claims description 3
ZFAIPBMPKVESPU-UHFFFAOYSA-N 2,3,4,5,6,7-hexafluoro-9,9-bis(methoxymethyl)fluorene Chemical compound C1=C(F)C(F)=C(F)C2=C1C(COC)(COC)C1=CC(F)=C(F)C(F)=C12 ZFAIPBMPKVESPU-UHFFFAOYSA-N 0.000 claims description 3
LDAYPNRUDRHPCA-UHFFFAOYSA-N 2,7-dicyclopentyl-9,9-bis(methoxymethyl)fluorene Chemical compound C1=C2C(COC)(COC)C3=CC(C4CCCC4)=CC=C3C2=CC=C1C1CCCC1 LDAYPNRUDRHPCA-UHFFFAOYSA-N 0.000 claims description 3
UURZCHPNAPLYER-UHFFFAOYSA-N 4-tert-butyl-9,9-bis(methoxymethyl)fluorene Chemical compound C1=CC=C(C(C)(C)C)C2=C1C(COC)(COC)C1=CC=CC=C12 UURZCHPNAPLYER-UHFFFAOYSA-N 0.000 claims description 3
NUPABKVXQKZAHY-UHFFFAOYSA-N 5,5-bis(methoxymethyl)-1,2,3,4-tetramethylcyclopenta-1,3-diene Chemical compound COCC1(COC)C(C)=C(C)C(C)=C1C NUPABKVXQKZAHY-UHFFFAOYSA-N 0.000 claims description 3
DNQBFNSYXQGWEA-UHFFFAOYSA-N 5,5-bis(methoxymethyl)cyclopenta-1,3-diene Chemical compound COCC1(COC)C=CC=C1 DNQBFNSYXQGWEA-UHFFFAOYSA-N 0.000 claims description 3
TYYSEGNSDSKJDW-UHFFFAOYSA-N 7-cyclohexyl-1,1-bis(methoxymethyl)indene Chemical compound C=12C(COC)(COC)C=CC2=CC=CC=1C1CCCCC1 TYYSEGNSDSKJDW-UHFFFAOYSA-N 0.000 claims description 3
OEGBIJMAWUHNFV-UHFFFAOYSA-N 7-cyclopentyl-1,1-bis(methoxymethyl)indene Chemical compound C=12C(COC)(COC)C=CC2=CC=CC=1C1CCCC1 OEGBIJMAWUHNFV-UHFFFAOYSA-N 0.000 claims description 3
XBHBMIOEDQWGPY-UHFFFAOYSA-N 7-tert-butyl-1,1-bis(methoxymethyl)indene Chemical compound C1=CC(C(C)(C)C)=C2C(COC)(COC)C=CC2=C1 XBHBMIOEDQWGPY-UHFFFAOYSA-N 0.000 claims description 3
UMMOCVFWWKDPNL-UHFFFAOYSA-N 9,9-bis(methoxymethyl)-1,2,3,4,5,6,7,8-octahydrofluorene Chemical compound C1CCCC2=C1C(COC)(COC)C1=C2CCCC1 UMMOCVFWWKDPNL-UHFFFAOYSA-N 0.000 claims description 3
MGQOPBZMDMTUQK-UHFFFAOYSA-N 9,9-bis(methoxymethyl)-1,2,3,4-tetrahydrofluorene Chemical compound C12=CC=CC=C2C(COC)(COC)C2=C1CCCC2 MGQOPBZMDMTUQK-UHFFFAOYSA-N 0.000 claims description 3
BJBJQWLYAGUTIO-UHFFFAOYSA-N 9,9-bis(methoxymethyl)-2,3,6,7-tetramethylfluorene Chemical compound CC1=C(C)C=C2C(COC)(COC)C3=CC(C)=C(C)C=C3C2=C1 BJBJQWLYAGUTIO-UHFFFAOYSA-N 0.000 claims description 3
PQRUIZPAUUOIPY-UHFFFAOYSA-N 9,9-bis(methoxymethyl)-2,7-di(propan-2-yl)fluorene Chemical compound C1=C(C(C)C)C=C2C(COC)(COC)C3=CC(C(C)C)=CC=C3C2=C1 PQRUIZPAUUOIPY-UHFFFAOYSA-N 0.000 claims description 3
UVZNCPVTOYWJAQ-UHFFFAOYSA-N 9,9-bis(methoxymethyl)xanthene Chemical group C1=CC=C2C(COC)(COC)C3=CC=CC=C3OC2=C1 UVZNCPVTOYWJAQ-UHFFFAOYSA-N 0.000 claims description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 3
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
JSDWVMORIKLNNU-UHFFFAOYSA-N [3,3-bis(methoxymethyl)-2,4,5-triphenylcyclopenta-1,4-dien-1-yl]benzene Chemical compound COCC1(COC)C(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)C(C=2C=CC=CC=2)=C1C1=CC=CC=C1 JSDWVMORIKLNNU-UHFFFAOYSA-N 0.000 claims description 3
DFBNDURJLQVNJX-UHFFFAOYSA-N [3,3-bis(methoxymethyl)inden-4-yl]-trimethylsilane Chemical compound C1=CC([Si](C)(C)C)=C2C(COC)(COC)C=CC2=C1 DFBNDURJLQVNJX-UHFFFAOYSA-N 0.000 claims description 3
150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 3
125000004429 atom Chemical group 0.000 claims description 3
150000001993 dienes Chemical class 0.000 claims description 3
150000003377 silicon compounds Chemical class 0.000 claims description 3
239000011593 sulfur Substances 0.000 claims description 3
UFMBYFXYRLFVPN-UHFFFAOYSA-N 1,1-bis[methoxy(phenyl)methyl]indene Chemical compound C1=CC2=CC=CC=C2C1(C(OC)C=1C=CC=CC=1)C(OC)C1=CC=CC=C1 UFMBYFXYRLFVPN-UHFFFAOYSA-N 0.000 claims description 2
POWUJINVZSHIGY-UHFFFAOYSA-N 2,6-di(propan-2-yl)piperidine Chemical group CC(C)C1CCCC(C(C)C)N1 POWUJINVZSHIGY-UHFFFAOYSA-N 0.000 claims description 2
OQYGKBOREGNKLC-UHFFFAOYSA-N 7-tert-butyl-1,1-bis(methoxymethyl)-2-methylindene Chemical compound C1=CC(C(C)(C)C)=C2C(COC)(COC)C(C)=CC2=C1 OQYGKBOREGNKLC-UHFFFAOYSA-N 0.000 claims description 2
MHOBTJZEFPKMLE-UHFFFAOYSA-N 9,9-bis(methoxymethyl)-2,3,6,7-tetramethylxanthene Chemical compound CC1=C(C)C=C2C(COC)(COC)C3=CC(C)=C(C)C=C3OC2=C1 MHOBTJZEFPKMLE-UHFFFAOYSA-N 0.000 claims description 2
QBVOFHFIKBUUMY-UHFFFAOYSA-N 9,9-bis[methoxy(phenyl)methyl]fluorene Chemical compound C12=CC=CC=C2C2=CC=CC=C2C1(C(OC)C=1C=CC=CC=1)C(OC)C1=CC=CC=C1 QBVOFHFIKBUUMY-UHFFFAOYSA-N 0.000 claims description 2
FBGWXZDLLURWAM-UHFFFAOYSA-N 9-(ethoxymethyl)-9-(methoxymethyl)fluorene Chemical compound C1=CC=C2C(COCC)(COC)C3=CC=CC=C3C2=C1 FBGWXZDLLURWAM-UHFFFAOYSA-N 0.000 claims description 2
239000002879 Lewis base Substances 0.000 claims description 2
229910052785 arsenic Inorganic materials 0.000 claims description 2
150000001733 carboxylic acid esters Chemical group 0.000 claims description 2
238000000605 extraction Methods 0.000 claims description 2
150000007527 lewis bases Chemical class 0.000 claims description 2
238000006467 substitution reaction Methods 0.000 claims description 2
229910052718 tin Inorganic materials 0.000 claims description 2
RMXREGKBZYAVSC-UHFFFAOYSA-N 1,1-bis(methoxymethyl)-7-(trifluoromethyl)indene Chemical compound C1=CC(C(F)(F)F)=C2C(COC)(COC)C=CC2=C1 RMXREGKBZYAVSC-UHFFFAOYSA-N 0.000 claims 2
LRFVTYWOQMYALW-UHFFFAOYSA-N 9H-xanthine Chemical compound O=C1NC(=O)NC2=C1NC=N2 LRFVTYWOQMYALW-UHFFFAOYSA-N 0.000 claims 2
125000004965 chloroalkyl group Chemical group 0.000 claims 2
LLVWLCAZSOLOTF-UHFFFAOYSA-N 1-methyl-4-[1,4,4-tris(4-methylphenyl)buta-1,3-dienyl]benzene Chemical compound C1=CC(C)=CC=C1C(C=1C=CC(C)=CC=1)=CC=C(C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 LLVWLCAZSOLOTF-UHFFFAOYSA-N 0.000 claims 1
WFLVIOIMYKVGLP-UHFFFAOYSA-N 9-(methoxymethyl)-9-(pentoxymethyl)fluorene Chemical compound C1=CC=C2C(COCCCCC)(COC)C3=CC=CC=C3C2=C1 WFLVIOIMYKVGLP-UHFFFAOYSA-N 0.000 claims 1
XNGIFLGASWRNHJ-UHFFFAOYSA-N o-dicarboxybenzene Natural products OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims 1
229940075420 xanthine Drugs 0.000 claims 1
229920001155 polypropylene Polymers 0.000 description 40
239000004743 Polypropylene Substances 0.000 description 38
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 34
IMNFDUFMRHMDMM-UHFFFAOYSA-N anhydrous n-heptane Natural products CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 20
230000000052 comparative effect Effects 0.000 description 18
229920000642 polymer Polymers 0.000 description 18
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 16
238000003756 stirring Methods 0.000 description 15
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 14
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 14
229910052782 aluminium Inorganic materials 0.000 description 13
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 13
BHPDSAAGSUWVMP-UHFFFAOYSA-N 3,3-bis(methoxymethyl)-2,6-dimethylheptane Chemical compound COCC(C(C)C)(COC)CCC(C)C BHPDSAAGSUWVMP-UHFFFAOYSA-N 0.000 description 10
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 10
150000002170 ethers Chemical class 0.000 description 9
229910001629 magnesium chloride Inorganic materials 0.000 description 9
239000000047 product Substances 0.000 description 9
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 9
238000001914 filtration Methods 0.000 description 8
150000002430 hydrocarbons Chemical class 0.000 description 8
239000007788 liquid Substances 0.000 description 8
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 7
239000005977 Ethylene Substances 0.000 description 7
239000000178 monomer Substances 0.000 description 7
239000000725 suspension Substances 0.000 description 7
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
229920001577 copolymer Polymers 0.000 description 6
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 6
230000000694 effects Effects 0.000 description 6
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 6
PVWCLOAAEFMTLH-UHFFFAOYSA-N 4,4-bis(methoxymethyl)-2,6-dimethylheptane Chemical compound COCC(COC)(CC(C)C)CC(C)C PVWCLOAAEFMTLH-UHFFFAOYSA-N 0.000 description 5
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 5
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
239000011737 fluorine Substances 0.000 description 5
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 5
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 5
UWNADWZGEHDQAB-UHFFFAOYSA-N 2,5-dimethylhexane Chemical group CC(C)CCC(C)C UWNADWZGEHDQAB-UHFFFAOYSA-N 0.000 description 4
MGWAVDBGNNKXQV-UHFFFAOYSA-N diisobutyl phthalate Chemical compound CC(C)COC(=O)C1=CC=CC=C1C(=O)OCC(C)C MGWAVDBGNNKXQV-UHFFFAOYSA-N 0.000 description 4
239000011521 glass Substances 0.000 description 4
238000004519 manufacturing process Methods 0.000 description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 4
239000012265 solid product Substances 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
HBMODDNTUPGVFW-UHFFFAOYSA-N (1,3-dimethoxy-2-phenylpropan-2-yl)benzene Chemical compound C=1C=CC=CC=1C(COC)(COC)C1=CC=CC=C1 HBMODDNTUPGVFW-UHFFFAOYSA-N 0.000 description 3
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 3
125000004135 2-norbornyl group Chemical group [H]C1([H])C([H])([H])C2([H])C([H])([H])C1([H])C([H])([H])C2([H])* 0.000 description 3
FJZBADSJNSFVDO-UHFFFAOYSA-N 3,3-bis(methoxymethyl)-2,4-dimethylpentane Chemical compound COCC(C(C)C)(C(C)C)COC FJZBADSJNSFVDO-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
229910010062 TiCl3 Inorganic materials 0.000 description 3
230000004888 barrier function Effects 0.000 description 3
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
JWCYDYZLEAQGJJ-UHFFFAOYSA-N dicyclopentyl(dimethoxy)silane Chemical compound C1CCCC1[Si](OC)(OC)C1CCCC1 JWCYDYZLEAQGJJ-UHFFFAOYSA-N 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
239000000706 filtrate Substances 0.000 description 3
125000005843 halogen group Chemical group 0.000 description 3
239000000155 melt Substances 0.000 description 3
229920005989 resin Polymers 0.000 description 3
239000011347 resin Substances 0.000 description 3
230000002194 synthesizing effect Effects 0.000 description 3
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
YONPGGFAJWQGJC-UHFFFAOYSA-K titanium(iii) chloride Chemical compound Cl[Ti](Cl)Cl YONPGGFAJWQGJC-UHFFFAOYSA-K 0.000 description 3
238000005406 washing Methods 0.000 description 3
BEDHCUAJOBASSZ-UHFFFAOYSA-N (2-cyclopentyl-1,3-dimethoxypropan-2-yl)cyclopentane Chemical compound C1CCCC1C(COC)(COC)C1CCCC1 BEDHCUAJOBASSZ-UHFFFAOYSA-N 0.000 description 2
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 2
RGHIYOCUMCUWAQ-UHFFFAOYSA-N 3,3-bis(methoxymethyl)-2,5-dimethylhexane Chemical compound COCC(COC)(CC(C)C)C(C)C RGHIYOCUMCUWAQ-UHFFFAOYSA-N 0.000 description 2
DNZXTVCIOVBBGV-UHFFFAOYSA-N 5,5-bis(methoxymethyl)-2,8-dimethylnonane Chemical compound CC(C)CCC(COC)(CCC(C)C)COC DNZXTVCIOVBBGV-UHFFFAOYSA-N 0.000 description 2
IRIAEXORFWYRCZ-UHFFFAOYSA-N Butylbenzyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 IRIAEXORFWYRCZ-UHFFFAOYSA-N 0.000 description 2
YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
229930040373 Paraformaldehyde Natural products 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
229910000831 Steel Inorganic materials 0.000 description 2
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
238000002083 X-ray spectrum Methods 0.000 description 2
PQIDFVXMOZQINS-UHFFFAOYSA-N [1-methoxy-2-(methoxymethyl)-3-methylbutan-2-yl]cyclohexane Chemical compound COCC(COC)(C(C)C)C1CCCCC1 PQIDFVXMOZQINS-UHFFFAOYSA-N 0.000 description 2
RHBLISBUFROBBC-UHFFFAOYSA-N [9-(hydroxymethyl)fluoren-9-yl]methanol Chemical compound C1=CC=C2C(CO)(CO)C3=CC=CC=C3C2=C1 RHBLISBUFROBBC-UHFFFAOYSA-N 0.000 description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
230000009918 complex formation Effects 0.000 description 2
238000002425 crystallisation Methods 0.000 description 2
230000008025 crystallization Effects 0.000 description 2
125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
MTZQAGJQAFMTAQ-UHFFFAOYSA-N ethyl benzoate Chemical compound CCOC(=O)C1=CC=CC=C1 MTZQAGJQAFMTAQ-UHFFFAOYSA-N 0.000 description 2
229920001038 ethylene copolymer Polymers 0.000 description 2
NIHNNTQXNPWCJQ-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical class ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 2
239000011261 inert gas Substances 0.000 description 2
229910052809 inorganic oxide Inorganic materials 0.000 description 2
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 2
239000003350 kerosene Substances 0.000 description 2
150000002681 magnesium compounds Chemical class 0.000 description 2
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 2
229920002866 paraformaldehyde Polymers 0.000 description 2
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 2
150000003021 phthalic acid derivatives Chemical class 0.000 description 2
230000000379 polymerizing effect Effects 0.000 description 2
239000011734 sodium Substances 0.000 description 2
238000001228 spectrum Methods 0.000 description 2
239000010959 steel Substances 0.000 description 2
CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 2
229910052719 titanium Inorganic materials 0.000 description 2
239000004711 α-olefin Substances 0.000 description 2
NOAIBMQZUGBONL-UHFFFAOYSA-N (1,3-dimethoxy-2-methylpropan-2-yl)benzene Chemical compound COCC(C)(COC)C1=CC=CC=C1 NOAIBMQZUGBONL-UHFFFAOYSA-N 0.000 description 1
HPOWOWTVWZELDK-UHFFFAOYSA-N (1,3-dimethoxy-2-methylpropan-2-yl)cyclohexane Chemical compound COCC(C)(COC)C1CCCCC1 HPOWOWTVWZELDK-UHFFFAOYSA-N 0.000 description 1
NXDUWPUPBXRKTJ-UHFFFAOYSA-N (2-benzyl-1,3-dimethoxypropan-2-yl)benzene Chemical compound C=1C=CC=CC=1C(COC)(COC)CC1=CC=CC=C1 NXDUWPUPBXRKTJ-UHFFFAOYSA-N 0.000 description 1
MEPSBRTXOHFWCF-UHFFFAOYSA-N (2-cyclohexyl-1,3-dimethoxypropan-2-yl)cyclohexane Chemical compound C1CCCCC1C(COC)(COC)C1CCCCC1 MEPSBRTXOHFWCF-UHFFFAOYSA-N 0.000 description 1
SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
TYMQLMOYWCNGJW-UHFFFAOYSA-N 1,1-bis(methoxymethyl)-2h-naphthalene Chemical compound C1=CC=C2C(COC)(COC)CC=CC2=C1 TYMQLMOYWCNGJW-UHFFFAOYSA-N 0.000 description 1
OSTKQRYZSROERR-UHFFFAOYSA-N 1,1-bis(methoxymethyl)-3,6-dimethylindene Chemical compound C1=C(C)C=C2C(COC)(COC)C=C(C)C2=C1 OSTKQRYZSROERR-UHFFFAOYSA-N 0.000 description 1
ZKXOLTKRGCQGJN-UHFFFAOYSA-N 1,1-bis(methoxymethyl)-4,5,6,7-tetrahydroindene Chemical compound C1CCCC2=C1C(COC)(COC)C=C2 ZKXOLTKRGCQGJN-UHFFFAOYSA-N 0.000 description 1
OGMUHNYKQFIZMP-UHFFFAOYSA-N 1,1-bis(methoxymethyl)-4,7-dimethyl-4,5,6,7-tetrahydroindene Chemical compound CC1CCC(C)C2=C1C(COC)(COC)C=C2 OGMUHNYKQFIZMP-UHFFFAOYSA-N 0.000 description 1
SLWKIVRKLSDJDJ-UHFFFAOYSA-N 1,1-bis(methoxymethyl)-4-phenyl-2h-naphthalene Chemical compound C12=CC=CC=C2C(COC)(COC)CC=C1C1=CC=CC=C1 SLWKIVRKLSDJDJ-UHFFFAOYSA-N 0.000 description 1
REYOVQKLCXXZTD-UHFFFAOYSA-N 1,1-bis(methoxymethyl)-4-phenylindene Chemical compound COCC1(COC)C=CC2=C1C=CC=C2C1=CC=CC=C1 REYOVQKLCXXZTD-UHFFFAOYSA-N 0.000 description 1
CCLDGIOSEOHYTP-UHFFFAOYSA-N 1,1-bis(methoxymethyl)cyclopenta[a]naphthalene Chemical compound C1=CC=CC2=C3C(COC)(COC)C=CC3=CC=C21 CCLDGIOSEOHYTP-UHFFFAOYSA-N 0.000 description 1
MZECAZRMUYMCLS-UHFFFAOYSA-N 1,1-bis(phenoxymethyl)indene Chemical compound C1=CC2=CC=CC=C2C1(COC=1C=CC=CC=1)COC1=CC=CC=C1 MZECAZRMUYMCLS-UHFFFAOYSA-N 0.000 description 1
KWXZYQJINBQUCF-UHFFFAOYSA-N 1,2,3,4-tetrafluoro-5,5-bis(methoxymethyl)cyclopenta-1,3-diene Chemical compound COCC1(COC)C(F)=C(F)C(F)=C1F KWXZYQJINBQUCF-UHFFFAOYSA-N 0.000 description 1
CHRJZRDFSQHIFI-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;styrene Chemical compound C=CC1=CC=CC=C1.C=CC1=CC=CC=C1C=C CHRJZRDFSQHIFI-UHFFFAOYSA-N 0.000 description 1
WCUJSHMGPIGRDS-UHFFFAOYSA-N 1,3-dimethoxy-4,4-dimethylpentane Chemical compound COCCC(OC)C(C)(C)C WCUJSHMGPIGRDS-UHFFFAOYSA-N 0.000 description 1
CELOJHLXFPSJPH-UHFFFAOYSA-N 1,3-dimethoxypropan-2-ylbenzene Chemical compound COCC(COC)C1=CC=CC=C1 CELOJHLXFPSJPH-UHFFFAOYSA-N 0.000 description 1
NOWCPSTWMDNKTI-UHFFFAOYSA-N 1,3-dimethoxypropan-2-ylcyclohexane Chemical compound COCC(COC)C1CCCCC1 NOWCPSTWMDNKTI-UHFFFAOYSA-N 0.000 description 1
YDGNDCHPLHXQMK-UHFFFAOYSA-N 1-(1,3-dimethoxypropan-2-yl)-1,2,3,4,4a,5,6,7,8,8a-decahydronaphthalene Chemical compound C1CCCC2C(C(COC)COC)CCCC21 YDGNDCHPLHXQMK-UHFFFAOYSA-N 0.000 description 1
CZSRLUPMHPVIPA-UHFFFAOYSA-N 1-(1,3-dimethoxypropan-2-yl)-4-fluorobenzene Chemical compound COCC(COC)C1=CC=C(F)C=C1 CZSRLUPMHPVIPA-UHFFFAOYSA-N 0.000 description 1
NCTNEBZFFHGOIK-UHFFFAOYSA-N 1-(1,3-dimethoxypropan-2-yl)naphthalene Chemical compound C1=CC=C2C(C(COC)COC)=CC=CC2=C1 NCTNEBZFFHGOIK-UHFFFAOYSA-N 0.000 description 1
ZTVGJMMXVMDFCX-UHFFFAOYSA-N 1-[1,3-dimethoxy-2-(4-methylphenyl)propan-2-yl]-4-methylbenzene Chemical compound C=1C=C(C)C=CC=1C(COC)(COC)C1=CC=C(C)C=C1 ZTVGJMMXVMDFCX-UHFFFAOYSA-N 0.000 description 1
HPFWUWXYBFOJAD-UHFFFAOYSA-N 1-chloro-4-(1,3-dimethoxypropan-2-yl)benzene Chemical compound COCC(COC)C1=CC=C(Cl)C=C1 HPFWUWXYBFOJAD-UHFFFAOYSA-N 0.000 description 1
PUBYKMSPAJMOGX-UHFFFAOYSA-N 1-chloro-4-[2-(4-chlorophenyl)-1,3-dimethoxypropan-2-yl]benzene Chemical compound C=1C=C(Cl)C=CC=1C(COC)(COC)C1=CC=C(Cl)C=C1 PUBYKMSPAJMOGX-UHFFFAOYSA-N 0.000 description 1
OUPPKRIDJAMCCA-UHFFFAOYSA-N 1-methoxy-2-(methoxymethyl)-2,3-dimethylbutane Chemical compound COCC(C)(C(C)C)COC OUPPKRIDJAMCCA-UHFFFAOYSA-N 0.000 description 1
ROSQVPGTZCDBOC-UHFFFAOYSA-N 1-methoxy-2-(methoxymethyl)-2,4-dimethylpentane Chemical compound COCC(C)(COC)CC(C)C ROSQVPGTZCDBOC-UHFFFAOYSA-N 0.000 description 1
XAGXJWYEHBCLPN-UHFFFAOYSA-N 1-methoxy-2-(methoxymethyl)-2-methylbutane Chemical compound COCC(C)(CC)COC XAGXJWYEHBCLPN-UHFFFAOYSA-N 0.000 description 1
SVJCEDKUVMVBKM-UHFFFAOYSA-N 1-methoxy-2-(methoxymethyl)-2-methylpentane Chemical compound CCCC(C)(COC)COC SVJCEDKUVMVBKM-UHFFFAOYSA-N 0.000 description 1
NGMVWDKVVMVTTM-UHFFFAOYSA-N 1-methoxy-2-(methoxymethyl)-3-methylbutane Chemical compound COCC(C(C)C)COC NGMVWDKVVMVTTM-UHFFFAOYSA-N 0.000 description 1
FDLMLTYTOFIPCK-UHFFFAOYSA-N 1-methoxy-2-(methoxymethyl)-3-methylpentane Chemical compound CCC(C)C(COC)COC FDLMLTYTOFIPCK-UHFFFAOYSA-N 0.000 description 1
PPHMKLXXVBJEHR-UHFFFAOYSA-N 1-methoxy-2-(methoxymethyl)hexane Chemical compound CCCCC(COC)COC PPHMKLXXVBJEHR-UHFFFAOYSA-N 0.000 description 1
125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 description 1
YZEDLRIAPPHENY-UHFFFAOYSA-N 1-tert-butyl-4-(1,3-dimethoxypropan-2-yl)benzene Chemical compound COCC(COC)C1=CC=C(C(C)(C)C)C=C1 YZEDLRIAPPHENY-UHFFFAOYSA-N 0.000 description 1
YSHXOWBWPGODRD-UHFFFAOYSA-N 10,10-bis(methoxymethyl)-9h-anthracene Chemical compound C1=CC=C2C(COC)(COC)C3=CC=CC=C3CC2=C1 YSHXOWBWPGODRD-UHFFFAOYSA-N 0.000 description 1
ZSWGZRORGQKOBA-UHFFFAOYSA-N 10-tert-butyl-9,9-bis(methoxymethyl)acridine Chemical compound C1=CC=C2C(COC)(COC)C3=CC=CC=C3N(C(C)(C)C)C2=C1 ZSWGZRORGQKOBA-UHFFFAOYSA-N 0.000 description 1
MFUQPPUUTXFFHU-UHFFFAOYSA-N 11,11-bis(methoxymethyl)-5,6-dihydrodibenzo[1,2-a:1',2'-e][7]annulene Chemical compound C1CC2=CC=CC=C2C(COC)(COC)C2=CC=CC=C21 MFUQPPUUTXFFHU-UHFFFAOYSA-N 0.000 description 1
CFJDKBFSMUNWRA-UHFFFAOYSA-N 11,11-bis(methoxymethyl)dibenzo[1,2-a:1',2'-e][7]annulene Chemical compound C1=CC2=CC=CC=C2C(COC)(COC)C2=CC=CC=C21 CFJDKBFSMUNWRA-UHFFFAOYSA-N 0.000 description 1
LTMRRSWNXVJMBA-UHFFFAOYSA-L 2,2-diethylpropanedioate Chemical compound CCC(CC)(C([O-])=O)C([O-])=O LTMRRSWNXVJMBA-UHFFFAOYSA-L 0.000 description 1
OONQZFJQVHEJFR-UHFFFAOYSA-N 2,3,6,7-tetrafluoro-1,1-bis(methoxymethyl)indene Chemical compound C1=C(F)C(F)=C2C(COC)(COC)C(F)=C(F)C2=C1 OONQZFJQVHEJFR-UHFFFAOYSA-N 0.000 description 1
IJELOUNJJDDDAU-UHFFFAOYSA-N 2,3-dicyclopentyl-5,5-bis(methoxymethyl)cyclopenta-1,3-diene Chemical compound C1CCCC1C1=CC(COC)(COC)C=C1C1CCCC1 IJELOUNJJDDDAU-UHFFFAOYSA-N 0.000 description 1
YIBYCVPCWUSPQY-UHFFFAOYSA-N 2-(1,3-dimethoxypropyl)-1,1-dimethylcyclohexane Chemical compound COCCC(OC)C1CCCCC1(C)C YIBYCVPCWUSPQY-UHFFFAOYSA-N 0.000 description 1
LZZZFFYXZLMKDR-UHFFFAOYSA-N 3,3-bis(ethoxymethyl)pentane Chemical compound CCOCC(CC)(CC)COCC LZZZFFYXZLMKDR-UHFFFAOYSA-N 0.000 description 1
SBWACGDKPKXCRS-UHFFFAOYSA-N 3,3-bis(methoxymethyl)-2,2,4,4-tetramethylpentane Chemical compound COCC(C(C)(C)C)(C(C)(C)C)COC SBWACGDKPKXCRS-UHFFFAOYSA-N 0.000 description 1
MRCDMWYOQNUJCM-UHFFFAOYSA-N 3,3-bis(methoxymethyl)cyclohexa-1,4-diene Chemical compound COCC1(COC)C=CCC=C1 MRCDMWYOQNUJCM-UHFFFAOYSA-N 0.000 description 1
NDAOWAVNIYQCLK-UHFFFAOYSA-N 3,3-bis(methoxymethyl)heptane Chemical compound CCCCC(CC)(COC)COC NDAOWAVNIYQCLK-UHFFFAOYSA-N 0.000 description 1
SKWKIEFIPVHTHJ-UHFFFAOYSA-N 3,3-bis(methoxymethyl)pentane Chemical compound COCC(CC)(CC)COC SKWKIEFIPVHTHJ-UHFFFAOYSA-N 0.000 description 1
CWLWBZJFQCTHEY-UHFFFAOYSA-N 3,6-dicyclohexyl-1,1-bis(phenoxymethyl)indene Chemical compound C1=C(C2CCCCC2)C2=CC=C(C3CCCCC3)C=C2C1(COC=1C=CC=CC=1)COC1=CC=CC=C1 CWLWBZJFQCTHEY-UHFFFAOYSA-N 0.000 description 1
DNUJVGBNIXGTHC-UHFFFAOYSA-N 3,6-dihydro-2h-oxazine Chemical compound C1NOCC=C1 DNUJVGBNIXGTHC-UHFFFAOYSA-N 0.000 description 1
PYHOSWIHPZRHDU-UHFFFAOYSA-N 4,4-bis(butoxymethyl)-2,6-dimethylheptane Chemical compound CCCCOCC(CC(C)C)(CC(C)C)COCCCC PYHOSWIHPZRHDU-UHFFFAOYSA-N 0.000 description 1
VVEYETJZOMJKNK-UHFFFAOYSA-N 4,4-bis(ethoxymethyl)-2,6-dimethylheptane Chemical compound CCOCC(CC(C)C)(CC(C)C)COCC VVEYETJZOMJKNK-UHFFFAOYSA-N 0.000 description 1
DDONJMJAIMKSOS-UHFFFAOYSA-N 4,4-bis(ethoxymethyl)heptane Chemical compound CCOCC(CCC)(CCC)COCC DDONJMJAIMKSOS-UHFFFAOYSA-N 0.000 description 1
JOUCABCJPVTXNS-UHFFFAOYSA-N 4,4-bis(methoxymethyl)-1-phenyl-1h-naphthalene Chemical compound C12=CC=CC=C2C(COC)(COC)C=CC1C1=CC=CC=C1 JOUCABCJPVTXNS-UHFFFAOYSA-N 0.000 description 1
QKXKUNZWVMVMAL-UHFFFAOYSA-N 4,4-bis(methoxymethyl)-2,7-dimethyloctane Chemical compound COCC(CC(C)C)(COC)CCC(C)C QKXKUNZWVMVMAL-UHFFFAOYSA-N 0.000 description 1
LOGBQWSMOBPZEA-UHFFFAOYSA-N 4,4-bis(methoxymethyl)-3,5-dimethylheptane Chemical compound CCC(C)C(COC)(COC)C(C)CC LOGBQWSMOBPZEA-UHFFFAOYSA-N 0.000 description 1
WOLQDDKBJWHVQK-UHFFFAOYSA-N 4,4-bis(methoxymethyl)heptane Chemical compound CCCC(CCC)(COC)COC WOLQDDKBJWHVQK-UHFFFAOYSA-N 0.000 description 1
VXEGSRKPIUDPQT-UHFFFAOYSA-N 4-[4-(4-methoxyphenyl)piperazin-1-yl]aniline Chemical compound C1=CC(OC)=CC=C1N1CCN(C=2C=CC(N)=CC=2)CC1 VXEGSRKPIUDPQT-UHFFFAOYSA-N 0.000 description 1
LHBLDRAQSNFIEY-UHFFFAOYSA-N 4-cyclohexyl-1,1-bis(methoxymethyl)indene Chemical compound COCC1(COC)C=CC2=C1C=CC=C2C1CCCCC1 LHBLDRAQSNFIEY-UHFFFAOYSA-N 0.000 description 1
CWVKCYDPJZCDMC-UHFFFAOYSA-N 4-ethyl-1-methoxy-2-(methoxymethyl)-2-methyloctane Chemical compound CCCCC(CC)CC(C)(COC)COC CWVKCYDPJZCDMC-UHFFFAOYSA-N 0.000 description 1
VIJVFTUOJNTXCA-UHFFFAOYSA-N 4-ethyl-1-methoxy-2-(methoxymethyl)octane Chemical compound CCCCC(CC)CC(COC)COC VIJVFTUOJNTXCA-UHFFFAOYSA-N 0.000 description 1
NDTLNHGFAUSCAE-UHFFFAOYSA-N 5,5-bis(ethoxymethyl)nonane Chemical compound CCCCC(CCCC)(COCC)COCC NDTLNHGFAUSCAE-UHFFFAOYSA-N 0.000 description 1
WUTBIESYSBKEFV-UHFFFAOYSA-N 5,6-dichloro-1,1-bis(1-methoxyethyl)indene Chemical compound ClC1=C(Cl)C=C2C(C(C)OC)(C(C)OC)C=CC2=C1 WUTBIESYSBKEFV-UHFFFAOYSA-N 0.000 description 1
IRVLICZNRLVVKJ-UHFFFAOYSA-N 5,9-diethyl-7,7-bis(methoxymethyl)tridecane Chemical compound CCCCC(CC)CC(COC)(COC)CC(CC)CCCC IRVLICZNRLVVKJ-UHFFFAOYSA-N 0.000 description 1
YFBQIUNHGZYHKD-UHFFFAOYSA-N 5-(1-methoxyethyl)-5-(methoxymethyl)-1,2,3,4-tetramethylcyclopenta-1,3-diene Chemical compound COCC1(C(C)OC)C(C)=C(C)C(C)=C1C YFBQIUNHGZYHKD-UHFFFAOYSA-N 0.000 description 1
VLXMQJNMOCEIRK-UHFFFAOYSA-N 7,7-bis(methoxymethyl)bicyclo[2.2.1]hepta-2,5-diene Chemical compound C1=CC2C=CC1C2(COC)COC VLXMQJNMOCEIRK-UHFFFAOYSA-N 0.000 description 1
ZVZZZVGNDBKCQC-UHFFFAOYSA-N 7,7-bis(methoxymethyl)cyclohepta-1,3,5-triene Chemical compound COCC1(COC)C=CC=CC=C1 ZVZZZVGNDBKCQC-UHFFFAOYSA-N 0.000 description 1
VOJHJALZRBMLDE-UHFFFAOYSA-N 9,9-bis(1-methoxyethyl)fluorene Chemical compound C1=CC=C2C(C(C)OC)(C(C)OC)C3=CC=CC=C3C2=C1 VOJHJALZRBMLDE-UHFFFAOYSA-N 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
DKMROQRQHGEIOW-UHFFFAOYSA-N Diethyl succinate Chemical compound CCOC(=O)CCC(=O)OCC DKMROQRQHGEIOW-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical class OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
VDZDYDLIDXQASZ-UHFFFAOYSA-N [1-cyclohexyl-3-methoxy-2-(methoxymethyl)propan-2-yl]cyclohexane Chemical compound C1CCCCC1C(COC)(COC)CC1CCCCC1 VDZDYDLIDXQASZ-UHFFFAOYSA-N 0.000 description 1
XMYDKOZNENQEHO-UHFFFAOYSA-N [1-methoxy-2-(methoxymethyl)-3-methylbutan-2-yl]cyclopentane Chemical compound COCC(COC)(C(C)C)C1CCCC1 XMYDKOZNENQEHO-UHFFFAOYSA-N 0.000 description 1
HLXKHZZBHUAIQI-UHFFFAOYSA-N [2,2-bis(methoxymethyl)-3-methylbutyl]cyclohexane Chemical compound COCC(COC)(C(C)C)CC1CCCCC1 HLXKHZZBHUAIQI-UHFFFAOYSA-N 0.000 description 1
ZVGIBQMBZHWERX-UHFFFAOYSA-N [2-(cyclohexylmethyl)-3-methoxy-2-(methoxymethyl)propyl]cyclohexane Chemical compound C1CCCCC1CC(COC)(COC)CC1CCCCC1 ZVGIBQMBZHWERX-UHFFFAOYSA-N 0.000 description 1
RORSEGNGPOMSSV-UHFFFAOYSA-N [3,3-bis(methoxymethyl)-5-phenylpentyl]benzene Chemical compound C=1C=CC=CC=1CCC(COC)(COC)CCC1=CC=CC=C1 RORSEGNGPOMSSV-UHFFFAOYSA-N 0.000 description 1
WVEZHRZEAFZJOI-UHFFFAOYSA-N [3-methoxy-2-(methoxymethyl)-1-phenylpropyl]benzene Chemical compound C=1C=CC=CC=1C(C(COC)COC)C1=CC=CC=C1 WVEZHRZEAFZJOI-UHFFFAOYSA-N 0.000 description 1
ZOUNQYODSPCWEH-UHFFFAOYSA-N [4-methoxy-3-(methoxymethyl)-2-methylbutan-2-yl]benzene Chemical compound COCC(COC)C(C)(C)C1=CC=CC=C1 ZOUNQYODSPCWEH-UHFFFAOYSA-N 0.000 description 1
JXQCBJLNEGKSCN-UHFFFAOYSA-N [4-methoxy-3-(methoxymethyl)butyl]benzene Chemical compound COCC(COC)CCC1=CC=CC=C1 JXQCBJLNEGKSCN-UHFFFAOYSA-N 0.000 description 1
AWLBWJXVYGYRNY-UHFFFAOYSA-N [4-methoxy-3-(methoxymethyl)butyl]cyclohexane Chemical compound COCC(COC)CCC1CCCCC1 AWLBWJXVYGYRNY-UHFFFAOYSA-N 0.000 description 1
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical group [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 1
230000004913 activation Effects 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
230000029936 alkylation Effects 0.000 description 1
238000005804 alkylation reaction Methods 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
150000001502 aryl halides Chemical class 0.000 description 1
238000006254 arylation reaction Methods 0.000 description 1
239000002585 base Substances 0.000 description 1
UXXXZMDJQLPQPH-UHFFFAOYSA-N bis(2-methylpropyl) carbonate Chemical compound CC(C)COC(=O)OCC(C)C UXXXZMDJQLPQPH-UHFFFAOYSA-N 0.000 description 1
125000006226 butoxyethyl group Chemical group 0.000 description 1
239000003990 capacitor Substances 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
101150102523 cdc12 gene Proteins 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
229940099352 cholate Drugs 0.000 description 1
ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 description 1
DWNAQMUDCDVSLT-UHFFFAOYSA-N diphenyl phthalate Chemical compound C=1C=CC=C(C(=O)OC=2C=CC=CC=2)C=1C(=O)OC1=CC=CC=C1 DWNAQMUDCDVSLT-UHFFFAOYSA-N 0.000 description 1
125000005982 diphenylmethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
238000004821 distillation Methods 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
NWPWRAWAUYIELB-UHFFFAOYSA-N ethyl 4-methylbenzoate Chemical compound CCOC(=O)C1=CC=C(C)C=C1 NWPWRAWAUYIELB-UHFFFAOYSA-N 0.000 description 1
YCNSGSUGQPDYTK-UHFFFAOYSA-N ethyl phenyl carbonate Chemical compound CCOC(=O)OC1=CC=CC=C1 YCNSGSUGQPDYTK-UHFFFAOYSA-N 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
238000004817 gas chromatography Methods 0.000 description 1
238000003987 high-resolution gas chromatography Methods 0.000 description 1
238000010813 internal standard method Methods 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
150000002596 lactones Chemical class 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
239000002245 particle Substances 0.000 description 1
125000004437 phosphorous atom Chemical group 0.000 description 1
125000005936 piperidyl group Chemical group 0.000 description 1
150000004291 polyenes Chemical class 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920001384 propylene homopolymer Polymers 0.000 description 1
125000000719 pyrrolidinyl group Chemical group 0.000 description 1
238000004445 quantitative analysis Methods 0.000 description 1
238000004062 sedimentation Methods 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000005049 silicon tetrachloride Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
239000012798 spherical particle Substances 0.000 description 1
150000003900 succinic acid esters Chemical class 0.000 description 1
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 1
239000008096 xylene 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
- 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

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)
Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)

NO960669A 1995-02-21 1996-02-20 Katalysatorbestanddel og katalysatorer for polymerisering av olefiner, samt fremgangsmåte for polymerisering av olefiner NO309380B1 (no)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
IT95MI000318 IT1274252B (it)	1995-02-21	1995-02-21	Catalizzatori per la polimerizzazione delle olefine
ITMI950317 IT1274251B (it)	1995-02-21	1995-02-21	Componenti e catalizzatori per la polimerizzazione delle olefine

Publications (3)

Publication Number	Publication Date
NO960669D0 NO960669D0 (no)	1996-02-20
NO960669L NO960669L (no)	1996-08-22
NO309380B1 true NO309380B1 (no)	2001-01-22

Family

ID=26331244

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO960669A NO309380B1 (no)	1995-02-21	1996-02-20	Katalysatorbestanddel og katalysatorer for polymerisering av olefiner, samt fremgangsmåte for polymerisering av olefiner

Country Status (20)

Country	Link
EP (1)	EP0728769B1 (de)
JP (1)	JP3904117B2 (de)
KR (1)	KR100424925B1 (de)
CN (1)	CN1090194C (de)
AR (1)	AR000994A1 (de)
AT (1)	ATE169937T1 (de)
AU (1)	AU699522B2 (de)
BR (1)	BR9600767A (de)
CA (1)	CA2169401C (de)
DE (1)	DE69600532T2 (de)
ES (1)	ES2121446T3 (de)
FI (1)	FI119643B (de)
HK (1)	HK1010379A1 (de)
HU (1)	HU221228B1 (de)
IL (1)	IL117114A (de)
IN (1)	IN186169B (de)
MY (1)	MY115716A (de)
NO (1)	NO309380B1 (de)
RU (1)	RU2156260C2 (de)
UA (1)	UA60290C2 (de)

Families Citing this family (331)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NL1003013C2 (nl) *	1996-05-03	1997-11-06	Dsm Nv	Met cyclische groepen gesubstitueerde cyclopentadieenverbinding.
US6117811A (en) *	1996-05-03	2000-09-12	Dsm N.V.	Cyclopentadiene compound substituted with linear groups
NL1003007C2 (nl) *	1996-05-03	1997-11-06	Dsm Nv	Met vertakte alkylgroepen gesubstitueerde cyclopentadieenverbinding.
NL1003017C2 (nl) *	1996-05-03	1997-11-06	Dsm Nv	Met een heteroatoom-bevattende groep gesubstitueerd fluoreen.
NL1003018C2 (nl) *	1996-05-03	1997-11-06	Dsm Nv	Met een heteroatoom-bevattende groep gesubstitueerde indeen.
NL1003008C2 (nl) *	1996-05-03	1997-11-06	Dsm Nv	Met een heteroatoom-bevattende groep gesubstitueerde cyclopentadieen- verbinding.
US6124488A (en) *	1996-05-03	2000-09-26	Dsm N.V.	Cyclopentadiene compound substituted with branched alkyl groups
NL1003011C2 (nl) *	1996-05-03	1997-11-06	Dsm Nv	Met een heteroatoom bevattende groep gesubstitueerde cyclopentadieen- verbinding.
NL1003004C2 (nl) *	1996-05-03	1997-11-06	Dsm Nv	Met onderling verschillende groepen gesubstitueerde cyclopentadieen- verbinding.
NL1003016C2 (nl) *	1996-05-03	1997-11-06	Dsm Nv	Gesubstitueerde pentadieenverbinding.
MY125673A (en) *	1996-06-10	2006-08-30	Mitsui Chemicals Inc	Solid titanium catalyst component for olefin polymerization,process for preparing the same, olefin plymerization catalyst containing the catalyst component and olefin polymerization process using thecatalyst
FI963707A0 (fi)	1996-09-19	1996-09-19	Borealis Polymers Oy	Foerfarande foer polymerisering av alfa-olefiner, vid polymerisering anvaendbar katalysator och foerfarande foer framstaellning av densamma
AU759295B2 (en) *	1998-05-06	2003-04-10	Montell Technology Company B.V.	Catalyst components for the polymerization of olefins
HUP0004633A3 (en)	1998-07-08	2003-07-28	Montell Technology Company Bv	Process and apparatus for the gas-phase polymerisation
BR9915469B1 (pt)	1998-08-20	2009-01-13		composiÇÕes copolimÉricas cristalinas de propileno, processo para preparar composiÇÕes copolimÉricas e filme ou folha monocamada ou multicamadas compreendendo ditas composiÇÕes polimÉricas.
DE69940340D1 (de)	1998-12-24	2009-03-12	Basell Poliolefine Srl	Flaschenverschlüsse aus polyolefinen
ES2208301T3 (es)	1999-03-09	2004-06-16	Basell Polyolefine Gmbh	Procedimiento multietapa para la (co)polimerizacion de olefinas.
CA2349297C (en)	1999-09-14	2008-11-18	Baselltech Usa Inc.	Impact-resistant polyolefin compositions
CN1137155C (zh)	1999-12-06	2004-02-04	中国石油化工集团公司	用于烯烃聚合或共聚合的催化剂体系
AR028493A1 (es)	1999-12-16	2003-05-14	Baselltech Usa Inc	Composiciones de copolimeros aleatorios de propileno que contienen una alfa-olefina como comonomero, procedimiento para producir la composicion, peliculas y articulos
US6673869B2 (en)	2000-07-27	2004-01-06	Basell Poliolefine Italia S.P.A.	Transparent elastomeric thermoplastic polyolefin compositions
KR20020060740A (ko)	2000-09-15	2002-07-18	리챠트 블라이스	올레핀 중합체에 대한 첨가제의 비압출 분산액 및 농축물
US6586531B2 (en)	2000-10-04	2003-07-01	Basell Poliolefine Italia S.P.A.	Polyolefin masterbatch and composition suitable for injection molding
JP2002173504A (ja) *	2000-11-29	2002-06-21	Basell Technology Co Bv	オレフィン重合用触媒およびオレフィン重合方法
JP4149809B2 (ja)	2000-12-15	2008-09-17	バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ	α−オレフィン重合用の固形触媒成分の連続製造方法
JP2004516373A (ja)	2000-12-22	2004-06-03	バセルポリオレフィンイタリアエス．ピー．エー．	熱成形用ポリオレフィンシート
TWI238169B (en)	2000-12-22	2005-08-21	Basell Technology Co Bv	Bioriented polypropylene films
EP1279699A1 (de)	2001-07-27	2003-01-29	Baselltech USA Inc.	Weiche Polyolefinzusammensetzungen
MY132768A (en)	2001-10-09	2007-10-31	Basell Poliolefine Italia Spa	Crystalline propylene copolymer compositions having improved sealability and optical properties and reduced solubility.
KR20040062605A (ko)	2001-10-30	2004-07-07	바셀 폴리올레핀 이탈리아 에스.피.에이.	폴리프로필렌 조성물의 파이프 시스템
RU2296772C2 (ru)	2001-11-27	2007-04-10	Базелль Полиолефин Италия С.П.А.	Прозрачная и гибкая композиция пропиленовых полимеров и изделие, полученное из нее
TWI268939B (en)	2001-12-12	2006-12-21	Basell Poliolefine Spa	Process for the polymerization of olefins
DE60326212D1 (de) *	2002-03-08	2009-04-02	Basell Poliolefine Srl	Verfahren zur herstellung einer katalysatorkomponente basierend auf einem diether
JP2005519172A (ja)	2002-03-08	2005-06-30	バセル　ポリオレフィン　イタリア　エス．ピー．エー．	オレフィンの重合方法
US6743864B2 (en)	2002-03-12	2004-06-01	Basell Poliolefine Italia S.P.A.	Polyolefin compositions having high tenacity
KR20040104474A (ko)	2002-03-12	2004-12-10	바셀 폴리올레핀 이탈리아 에스.피.에이.	고유동성을 갖는 폴리올레핀 조성물
BR0305248A (pt)	2002-06-26	2004-09-21	Basell Poliolefine Spa	Composições de poliolefinas resistentes ao impacto
US7700690B2 (en)	2002-06-26	2010-04-20	Basell Poliolefine Italia S.R.L.	Impact-resistant polyolefin compositions
US7112642B2 (en)	2002-08-01	2006-09-26	Basell Poliolefine Italia S.P.A.	Highly stereoregular polypropylene with improved properties
KR20050042077A (ko)	2002-09-17	2005-05-04	바셀 폴리올레핀 이탈리아 에스.피.에이.	고충전 연성 폴리올레핀 조성물
MXPA05006585A (es) *	2002-12-18	2005-08-16	Basell Poliolefine Spa	Aductos basados en dicloruro de magnesio, y componentes de catalizador obtenidos de los mismos.
US7288598B2 (en)	2003-03-06	2007-10-30	Basell Poliolefine Italia S.P.A.	Polyolefin masterbatch for preparing impact-resistant polyolefin articles
MY136027A (en)	2003-04-02	2008-07-31	Basell Poliolefine Spa	Polyolefin masterbatch and composition suitable for injection molding
TW200427763A (en)	2003-04-03	2004-12-16	Basell Poliolefine Spa	Impact resistant polyolefin compositions
EP1651720B1 (de)	2003-08-05	2013-09-11	Basell Poliolefine Italia S.r.l.	Polyolefingegenstände
TW200505985A (en)	2003-08-07	2005-02-16	Basell Poliolefine Spa	Polyolefin composition having a high balance of stiffness and impact strength
AU2004287638A1 (en) *	2003-11-06	2005-05-19	Basell Poliolefine Italia S.R.L.	Polypropylene composition
CN1894448A (zh)	2003-12-19	2007-01-10	巴塞尔聚烯烃意大利有限责任公司	由丙烯和1－己烯的共聚物制造的纤维
JP4960858B2 (ja)	2004-03-03	2012-06-27	バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ	重合工程においてポリマーの流量を制御する方法
CA2561576A1 (en) *	2004-03-29	2005-10-13	Basell Poliolefine Italia S.R.L.	Magnesium chloride-based adducts and catalyst components obtained therefrom
WO2005113672A1 (en)	2004-05-21	2005-12-01	Basell Poliolefine Italia S.R.L.	Impact resistant polyolefin compositions
US8039540B2 (en)	2004-06-08	2011-10-18	Basell Poliolefine Italia S.R.L.	Polyolefin composition having a high balance of stiffness, impact strength and elongation at break and low thermal shrinkage
ES2343070T3 (es)	2004-06-18	2010-07-22	Basell Poliolefine Italia S.R.L.	Procedimiento para la preparacion de componentes catalizadores para la polimerizacion de olefinas.
JP2008503620A (ja)	2004-06-25	2008-02-07	バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ	プロピレン及びα−オレフィンのランダムコポリマーから製造したパイプシステム
CN101065437B (zh) †	2004-10-04	2010-12-08	巴塞尔聚烯烃意大利有限责任公司	弹性体聚烯烃组合物
US7652108B2 (en)	2004-10-14	2010-01-26	Basell Poliolefine Italia S.R.L.	Process for the gas-phase polymerization olefins
CN100389112C (zh) *	2004-12-16	2008-05-21	中国石油化工股份有限公司	一类环状缩醛和缩酮化合物及其应用
EP1827825A1 (de)	2004-12-21	2007-09-05	Basell Poliolefine Italia S.r.l.	Heissversiegelbare polyolefinfolien
BRPI0518119A (pt)	2004-12-23	2008-10-28	Basell Poliolefine Srl	composições poliolefìnicas tendo boa resistência ao branqueamento
JP2008528779A (ja)	2005-02-03	2008-07-31	バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ	射出成形用プロピレンポリマー組成物
WO2006114358A2 (en)	2005-04-28	2006-11-02	Basell Poliolefine Italia S.R.L.	Reinforced polypropylene pipe
DE602006007572D1 (de) *	2005-05-12	2009-08-13	Basell Poliolefine Srl	Propylen-ethylen-copolymere und herstellungsverfahren dafür
EP1896513B1 (de)	2005-05-13	2010-01-20	Basell Poliolefine Italia S.r.l.	Verfahren zur gasphasenpolymerisation von olefinen
RU2408623C2 (ru)	2005-05-27	2011-01-10	Базелль Полиолефин Италия С.Р.Л.	Полиолефиновые композиции, обладающие хорошей устойчивостью к белению
US9145495B2 (en)	2005-07-01	2015-09-29	Basell Poliolefine Italia S.R.L.	Propylene polymers having broad molecular weight distribution
RU2412823C2 (ru)	2005-07-11	2011-02-27	Базелль Полиолефин Италия С.Р.Л.	Металлизированная полипропиленовая пленка с хорошим сохранением барьерных свойств
JP5300486B2 (ja)	2005-11-22	2013-09-25	バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ	低い光沢を有するポリオレフィン組成物
US7872074B2 (en)	2005-11-22	2011-01-18	Basell Poliolefine Italia S.R.L.	Impact resistant polyolefin compositions
US7947348B2 (en)	2005-12-20	2011-05-24	Basell Poliolefine Italia, s.r.l.	Polypropylene compositions for stretched articles
WO2007096209A1 (en)	2006-02-23	2007-08-30	Basell Poliolefine Italia S.R.L.	Propylene polymers for injection molding applications
EP1845112A1 (de)	2006-04-12	2007-10-17	Total Petrochemicals Research Feluy	Kontrollierte Verteilung von reaktiven Stellen bei Ziegler-Natta Katalysatoren
WO2007147714A1 (en)	2006-06-23	2007-12-27	Basell Poliolefine Italia S.R.L.	Magnesium chloroalkolate-based catalyst precursors
TWI496762B (zh)	2006-07-24	2015-08-21		製備（１ｒ，２ｒ）-３-（３-二甲胺基-１-乙基-２-甲基-丙基）-酚之方法
EP2046845B1 (de)	2006-07-28	2012-06-06	Basell Poliolefine Italia S.r.l.	Propylenpolymere
DE602007008133D1 (de)	2006-11-23	2010-09-09	Basell Poliolefine Srl	Polyolefinzusammensetzungen
EP2089470B1 (de)	2006-12-07	2011-06-01	Basell Poliolefine Italia S.r.l.	Polyolefinzusammensetzungen mit geringer härte und geringem glanz
EP2089469B1 (de)	2006-12-07	2011-08-10	Basell Poliolefine Italia S.r.l.	Polyolefinzusammensetzungen mit geringer härte und geringem glanz
RU2441040C2 (ru)	2006-12-21	2012-01-27	Базелль Полиолефин Италия С.Р.Л.	Высокоусадочные полипропиленовые пленки
JP5583973B2 (ja)	2006-12-22	2014-09-03	バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ	オレフィン重合用の触媒成分及びそれから得られる触媒
EP2094780B1 (de)	2006-12-22	2010-10-20	Basell Poliolefine Italia S.R.L.	Polyolefinzusammensetzung für rohrsysteme und folien
EP2070956A1 (de)	2007-12-14	2009-06-17	Total Petrochemicals Research Feluy	Verfahren zur Herstellung eines bimodalen Polypropylens mit geringem Ascheanteil
EP2147026B1 (de)	2007-05-22	2010-10-20	Basell Poliolefine Italia S.r.l.	Weiche propylenpolymerzusammensetzungen
JP5518698B2 (ja)	2007-05-22	2014-06-11	バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ	軟質プロピレンポリマー組成物の製造方法
CN101323650B (zh)	2007-06-13	2010-11-03	中国石油天然气股份有限公司	一种烯烃聚合催化剂及其制备方法和应用
US10150828B2 (en) *	2007-08-03	2018-12-11	Basell Poliolefine Italia S.R.L.	Process for producing propylene terpolymers
CN101835812B (zh)	2007-08-24	2013-10-02	陶氏环球技术有限责任公司	具有受控的铝和选择性控制剂之比的自限制催化剂体系和方法
US7893003B2 (en)	2007-08-24	2011-02-22	Dow Global Technologies Inc.	Catalyst composition with mixed selectivity control agent and method
US8779058B2 (en)	2007-08-24	2014-07-15	William G. Sheard	High melt flow propylene impact copolymer and method
PL2197951T3 (pl)	2007-10-17	2011-07-29	Basell Poliolefine Italia Srl	Heterofazowe kompozycje poliolefinowe o ulepszonej rozciągliwości
JP5580743B2 (ja)	2007-11-27	2014-08-27	バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ	ビチューメンとポリマー組成物との混合物
EP2070954A1 (de)	2007-12-14	2009-06-17	Total Petrochemicals Research Feluy	Verfahren zur Herstellung eines Polypropylens mit breiter Molekulargewichtsverteilung und geringem Ascheanteil
CN101903424A (zh)	2007-12-18	2010-12-01	巴塞尔聚烯烃意大利有限责任公司	丙烯与己烯-1的共聚物和从其得到的吹塑膜
EP2222781B1 (de)	2007-12-18	2014-01-15	Basell Poliolefine Italia S.r.l.	Transparente polyolefinzusammensetzungen
EP2077286A1 (de)	2008-01-07	2009-07-08	Total Petrochemicals Research Feluy	Heterophasisches Propylencopolymer mit verbessertem Kriechverhalten
EP2247424B1 (de)	2008-02-29	2012-07-04	Basell Poliolefine Italia S.r.l.	Polyolefinzusammensetzungen
EP2141200A1 (de)	2008-07-03	2010-01-06	Total Petrochemicals Research Feluy	Heterophasisches Propylen-Copolymer mit verbesserten Eigenschaften für Injektionsformungsanwendungen
CN101735346B (zh)	2008-11-07	2012-05-30	中国石油天然气股份有限公司	一种丙烯均聚和共聚的催化剂及其制备方法和应用
US8623932B2 (en)	2008-12-17	2014-01-07	Basell Poliolefine Italia S.R.L.	Foamed polyolefin composition
RU2532182C2 (ru)	2008-12-24	2014-10-27	Базелль Полиолефин Италия С.Р.Л.	Напорные трубы и полиолефиновые композиции для их получения
RU2502746C2 (ru)	2008-12-31	2013-12-27	ДАУ ГЛОБАЛ ТЕКНОЛОДЖИЗ ЭлЭлСи	Прокаталитическая композиция с замещенным 1,2-фениленовым ароматическим сложнодиэфирным внутренним донором и способ
KR101695995B1 (ko)	2008-12-31	2017-01-12	더블유.알. 그레이스 앤드 캄파니-콘.	향상된 전촉매 조성물 및 방법
EP2230273A1 (de)	2009-03-09	2010-09-22	Total Petrochemicals Research Feluy	Polypropylenzusammensetzung in Blasfolie
EP2411464B1 (de)	2009-03-23	2013-05-08	Basell Poliolefine Italia S.r.l.	Polyolefin-masterbatch und für den spritzguss geeignete zusammensetzung
WO2010112337A1 (en)	2009-03-31	2010-10-07	Basell Poliolefine Italia S.R.L.	Polyolefin masterbatch and composition suitable for injection molding
KR101538910B1 (ko)	2009-05-21	2015-07-23	바셀 폴리올레핀 이탈리아 에스.알.엘	프로필렌 중합체 조성물
EP2264099A1 (de)	2009-05-21	2010-12-22	Basell Poliolefine Italia S.R.L.	Propylenpolymerzusammensetzungen
KR101769275B1 (ko)	2009-06-19	2017-08-18	바셀 폴리올레핀 이탈리아 에스.알.엘	내충격성 프로필렌 중합체 조성물의 제조 방법
KR20120093064A (ko)	2009-06-26	2012-08-22	바셀 폴리올레핀 이탈리아 에스.알.엘	폴리올레핀 조성물
WO2011009704A1 (en)	2009-07-21	2011-01-27	Basell Poliolefine Italia S.R.L.	Fibres made from copolymers of propylene and 1-pentene
EP2459642B1 (de)	2009-07-31	2016-12-07	Basell Poliolefine Italia S.r.l.	Polyolefinische zusammensetzungen
KR101831456B1 (ko)	2009-07-31	2018-02-22	바셀 폴리올레핀 이탈리아 에스.알.엘	폴리올레핀계 조성물
CN102741301B (zh)	2009-09-11	2014-10-08	巴塞尔聚烯烃意大利有限责任公司	烯烃的气相聚合方法
US8729188B2 (en)	2009-09-22	2014-05-20	Basell Poliolefine Italia S.R.L.	Propylene polymer compositions
EP2480604B1 (de)	2009-09-22	2017-03-01	Basell Poliolefine Italia S.r.l.	Propylenpolymerzusammensetzungen
US8569419B2 (en)	2009-09-22	2013-10-29	Basell Poliolefine Italia, s.r.l.	Propylene polymer compositions
WO2011036002A1 (en)	2009-09-22	2011-03-31	Basell Poliolefine Italia S.R.L.	Propylene polymer compositions
WO2011035994A1 (en)	2009-09-22	2011-03-31	Basell Poliolefine Italia S.R.L.	Propylene polymer compositions
WO2011036077A1 (en)	2009-09-24	2011-03-31	Basell Poliolefine Italia S.R.L.	Heat-sealable polyolefin films
WO2011039314A1 (en)	2009-09-29	2011-04-07	Basell Poliolefine Italia Srl	Heat-sealable polyolefin films
EP2305723A1 (de)	2009-10-01	2011-04-06	Total Petrochemicals Research Feluy	Propylenpolymer mit verbesserter Verarbeitbarkeit bei der Thermoformung
KR101765964B1 (ko)	2009-10-13	2017-08-07	바셀 폴리올레핀 이탈리아 에스.알.엘	프로필렌 중합체 조성물
BR112012010897B1 (pt)	2009-11-17	2019-09-10	Basell Poliolefine Italia Srl	"filmes termorretráteis"
EP2501727B1 (de)	2009-11-19	2014-05-14	Basell Poliolefine Italia S.r.l.	Verfahren für die herstellung von schlagfesten propylenpolymerzusammensetzungen
WO2011076553A1 (en)	2009-12-21	2011-06-30	Basell Poliolefine Italia S.R.L.	Impact-resistant polyolefin compositions
WO2011076555A1 (en)	2009-12-21	2011-06-30	Basell Poliolefine Italia S.R.L.	Impact-resistant polyolefin compositions
CN102686662B (zh)	2009-12-22	2015-11-25	巴塞尔聚烯烃意大利有限责任公司	用于膜的聚烯烃组合物
EP2516546B1 (de)	2009-12-23	2014-01-15	Basell Poliolefine Italia S.r.l.	Polyolefinzusammensetzungen für sprietzgussabflusssysteme
WO2011117032A1 (en)	2010-03-26	2011-09-29	Basell Poliolefine Italia Srl	Heterophasic polyolefin composition
US8785584B2 (en)	2010-04-14	2014-07-22	Basell Poliolefine Italia S.R.L.	Propylene-based terpolymers for films
JP2013525581A (ja) *	2010-05-05	2013-06-20	バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ	プロピレンポリマー組成物
WO2011144486A1 (en)	2010-05-19	2011-11-24	Basell Poliolefine Italia Srl	Polypropylene tub for washing machine
CN102884124B (zh)	2010-05-20	2015-02-18	巴塞尔聚烯烃意大利有限责任公司	丙烯聚合物组合物
CN102947356B (zh)	2010-06-22	2015-09-09	巴塞尔聚烯烃意大利有限责任公司	烯烃气相聚合的方法
EP2585527B1 (de)	2010-06-23	2015-01-14	Basell Poliolefine Italia S.r.l.	Polyolefinzusammensetzung für rohrsysteme und folien
WO2011160953A1 (en)	2010-06-23	2011-12-29	Basell Poliolefine Italia Srl	Polyolefin composition for pipe systems and sheets
CN102985479B (zh)	2010-06-23	2015-04-08	巴塞尔聚烯烃意大利有限责任公司	管材和用于制造其的聚烯烃组合物
EP2596060B1 (de)	2010-07-23	2014-05-28	Basell Poliolefine Italia S.r.l.	Propylenpolymerzusammensetzungen
US8974909B2 (en)	2010-07-29	2015-03-10	Basell Poliolefine Italia S.R.L.	Random copolymers of propylene
EP2614115B1 (de)	2010-09-06	2016-04-27	Basell Poliolefine Italia S.r.l.	Polyolefinzusammensetzungen mit verbesserter siegelfähigkeit
US9006368B2 (en)	2010-09-06	2015-04-14	Basell Poliolefine Italia S.R.L.	Propylene-based terpolymers for film
ES2627689T3 (es)	2010-09-06	2017-07-31	Basell Poliolefine Italia S.R.L.	Películas que comprenden terpolímeros en base a polipropileno
US9073027B2 (en)	2010-09-09	2015-07-07	Basell Poliolefine Italia S.R.L.	Process and apparatus for the gas-phase polymerization of olefins
BR112013008076B1 (pt)	2010-10-14	2020-06-09	Basell Poliolefine Italia Srl	elemento para o interior automotivo e uso de uma composição de polipropileno
CN102453133B (zh) *	2010-10-25	2013-06-05	中国石油化工股份有限公司	烯烃聚合催化剂体系及使用该催化剂体系的烯烃聚合方法
WO2012055742A2 (en)	2010-10-26	2012-05-03	Basell Poliolefine Italia S.R.L.	Process for producing injection stretch blow molded polyolefin containers
RU2581869C2 (ru)	2010-11-29	2016-04-20	Базелль Полиолефин Италия С.Р.Л.	Мембраны
EP2463413B1 (de)	2010-12-07	2014-01-29	Basell Poliolefine Italia S.r.l.	Polyolefinfasern
EP2648910B1 (de)	2010-12-09	2018-08-08	Basell Poliolefine Italia S.r.l.	Durchlässiger polymerfilm
WO2012099549A1 (en) *	2010-12-22	2012-07-26	Ptt Global Chemical Pcl	A magnesium halide support for use as a composition of a catalyst for the olefin polymerization, and method of preparation of the magnesium halide support
EP2665772B1 (de)	2011-01-18	2014-11-05	Basell Poliolefine Italia S.r.l.	Polyolefinzusammensetzung
EP2683771B1 (de)	2011-03-10	2015-04-15	Basell Poliolefine Italia S.r.l.	Behälter auf polyolefinbasis
EP2505606B1 (de)	2011-03-29	2017-03-01	Basell Poliolefine Italia S.r.l.	Polyolefinzusammensetzung für leitungssysteme
JP6005726B2 (ja)	2011-04-12	2016-10-12	バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ	オレフィン重合用の触媒成分
EP2699718B1 (de)	2011-04-21	2015-03-04	Basell Poliolefine Italia S.r.l.	Terpolymere auf propylenbasis für fasern
CN102746426A (zh)	2011-04-22	2012-10-24	中国石油天然气股份有限公司	一种烯烃聚合催化剂及其制备和应用
BR112013028699B1 (pt)	2011-05-11	2021-03-16	Basell Poliolefine Italia S.R.L	composições de poliolefina e de poliolefina enchida bem como artigos, folhas ou películas para cobertura e enchimento interno para cabos industriais ou embainhamento de cabos compreendendo as referidas composições
WO2013004507A1 (en)	2011-07-01	2013-01-10	Basell Poliolefine Italia S.R.L.	Polypropylene films and sheets
EP2729507B1 (de)	2011-07-06	2015-10-14	Basell Poliolefine Italia S.r.l.	Statistische copolymere von propylen mit hexen-1
BR112014000017B1 (pt)	2011-07-07	2020-04-07	Basell Poliolefine Italia Srl	composição de polipropileno
EP2731781B1 (de)	2011-07-15	2016-05-18	Basell Poliolefine Italia S.r.l.	Polyolefinstreifen mit einem statistischen copolymer aus propylen mit 1-hexen
CN103781614B (zh)	2011-09-01	2016-08-31	巴塞尔聚烯烃意大利有限责任公司	用于薄膜的基于丙烯的三元共聚物
WO2013041470A1 (en)	2011-09-23	2013-03-28	Basell Poliolefine Italia S.R.L.	Process for the preparation of high purity propylene polymers
EP2578628A1 (de)	2011-10-07	2013-04-10	Basell Poliolefine Italia S.r.l.	Propylenpolymerzusammensetzungen
EP2583999A1 (de)	2011-10-20	2013-04-24	Basell Poliolefine Italia S.r.l.	Polyolefinzusammensetzungen
EP2594593A1 (de)	2011-11-17	2013-05-22	Basell Poliolefine Italia S.r.l.	Verfahren zur Herstellung von heterophasischen Propylenpolymerzusammensetzungen
WO2013083576A1 (en)	2011-12-05	2013-06-13	Basell Poliolefine Italia S.R.L.	Propylene terpolymers
EP2602102A1 (de)	2011-12-05	2013-06-12	Basell Poliolefine Italia S.r.l.	Propylenbasierte Terpolymere für Rohre
EP2653496A1 (de)	2012-04-17	2013-10-23	Basell Polyolefine GmbH	Propylenbasierte Terpolymezusammensetzung für Rohre
RU2583372C1 (ru)	2011-12-05	2016-05-10	Базелль Полиолефин Италия С.Р.Л.	Композиции из тройных сополимеров на основе пропилена для труб
EP2610274A1 (de)	2011-12-30	2013-07-03	Borealis AG	Propylen-Zufallscopolymer
EP2639268A1 (de)	2012-03-13	2013-09-18	Basell Poliolefine Italia S.r.l.	Propylenpolymerzusammensetzungen
EP2639267A1 (de)	2012-03-13	2013-09-18	Basell Poliolefine Italia S.r.l.	Propylenpolymerzusammensetzungen
US9815918B2 (en)	2012-03-19	2017-11-14	Formosa Plastics Corporation, U.S.A.	Catalyst component for high activity and high stereoselectivity in olefin polymerization
EP2666793A1 (de)	2012-05-21	2013-11-27	Basell Poliolefine Italia S.r.l.	Terpolymer auf Propylenbasis
EP2679631A1 (de)	2012-06-27	2014-01-01	Total Research & Technology Feluy	Propylenhomopolymer für hochfeste Fasern und Vliesstoffe
DK2867295T3 (en)	2012-06-27	2016-02-01	Total Res & Technology Feluy Sa	PROPYLENE HOMOPOLYMES FOR FIBER AND NON-WOVEN HIGH TENACITY MATERIALS
WO2014001426A1 (en)	2012-06-27	2014-01-03	Total Research & Technology Feluy	Propylene polymer for high-tenacity fibers and nonwovens
EP2679609A1 (de)	2012-06-28	2014-01-01	Lummus Novolen Technology Gmbh	Steril anspruchsvolle Dialkoxydialkylsilane als externe Spender für Ziegler-Katalysatoren für die Polymerisation von Propylen
EP2682505A1 (de)	2012-07-06	2014-01-08	Basell Poliolefine Italia S.r.l.	Polypropylenfaser
CN103626893B (zh) *	2012-08-23	2016-03-30	中国石油化工股份有限公司	用于烯烃聚合反应的催化剂组分及其催化剂制备方法
CN103626895B (zh) *	2012-08-23	2016-03-30	中国石油化工股份有限公司	用于烯烃聚合反应的催化剂组分及其催化剂制备方法
CN103626894B (zh) *	2012-08-23	2016-03-30	中国石油化工股份有限公司	用于烯烃聚合反应的催化剂组分及其催化剂制备方法
EP2711379A1 (de)	2012-09-21	2014-03-26	Basell Poliolefine Italia S.r.l.	Verfahren zur Gasphasenpolymerisation von Olefinen
EP2722348A1 (de)	2012-10-16	2014-04-23	Basell Poliolefine Italia S.r.l.	Verfahren zur Herstellung von Random-Propylencopolymeren
EP2727959A1 (de)	2012-11-01	2014-05-07	Basell Poliolefine Italia S.r.l.	Propylenbasierte Terpolymezusammensetzung für Rohre
US9522968B2 (en)	2012-11-26	2016-12-20	Lummus Novolen Technology Gmbh	High performance Ziegler-Natta catalyst systems, process for producing such MgCl2 based catalysts and use thereof
US9481741B2 (en)	2012-11-26	2016-11-01	Lummus Novolen Technology Gmbh	High performance Ziegler-Natta catalyst systems, process for producing such supported catalysts and use thereof
EP2743073A1 (de)	2012-12-12	2014-06-18	Basell Poliolefine Italia S.r.l.	Propylenbaseirte Terpolymere
EP2743307A1 (de)	2012-12-12	2014-06-18	Basell Poliolefine Italia S.r.l.	Polyolefinzusammensetzung
EP2746297A1 (de)	2012-12-20	2014-06-25	Basell Poliolefine Italia S.r.l.	Magnesium-Dichlorid-Alkohol-Addukte und dadurch erhaltene Katalysatorkomponenten
EP2778265A1 (de)	2013-03-11	2014-09-17	Basell Polyolefine GmbH	Mehrschichtige Fasern
KR101768846B1 (ko)	2013-03-15	2017-08-17	바셀 폴리올레핀 이탈리아 에스.알.엘	프로필렌 삼원중합체의 제조 공정, 및 그에 의해 얻은 프로필렌 삼원중합체
US9284392B2 (en) *	2013-03-15	2016-03-15	Basf Corporation	Mixed internal donor structures for 1-olefin polymerization catalysts
EP2781548A1 (de)	2013-03-19	2014-09-24	Basell Poliolefine Italia S.r.l.	Mineralgefüllte Polypropylen-Zusammensetzung
EP2792692A1 (de)	2013-04-17	2014-10-22	Basell Poliolefine Italia S.r.l.	Nukleierte Polyolefinzusammensetzungen auf Propylenbasis
EP2803676A1 (de) *	2013-05-16	2014-11-19	Basell Polyolefine GmbH	Verfahren zur Gasphasenpolymerisation von Ethylen oder Ethylenmischungen
CN105408371B (zh)	2013-06-03	2017-10-13	鲁姆斯诺沃伦技术公司	高效齐格勒‑纳塔催化剂体系，该催化剂体系的生产方法及其应用
EP2813438A1 (de)	2013-06-11	2014-12-17	Basell Poliolefine Italia S.r.l.	Propylenbasierte Terpolymere
KR102082746B1 (ko) *	2013-06-11	2020-02-28	삼성전자주식회사	진공 청소기
EP2816062A1 (de)	2013-06-18	2014-12-24	Basell Poliolefine Italia S.r.l.	Vorpolymerisierte Katalysatorkomponenten zur Polymerisierung von Olefinen
US20160137761A1 (en)	2013-06-19	2016-05-19	Borealis Ag	Process for production of polypropylene with high polydispersity
CN105339424B (zh)	2013-06-19	2018-05-29	博里利斯股份公司	具有极宽分子量分布的聚丙烯
EP2829557A1 (de) *	2013-07-22	2015-01-28	Basell Poliolefine Italia S.r.l.	Sterilisierbare Artikel aus Propylencopolymer
EP2829397A1 (de)	2013-07-22	2015-01-28	Basell Poliolefine Italia S.r.l.	Heißversiegelbare Polyolefinfilme und Folien
JP6216887B2 (ja)	2013-08-14	2017-10-18	ボレアリス・アクチェンゲゼルシャフトＢｏｒｅａｌｉｓＡｇ	低温における耐衝撃性が改善されたプロピレン組成物
EA031054B1 (ru)	2013-08-21	2018-11-30	Бореалис Аг	Композиция полиолефина с высокой текучестью, жесткостью и ударной вязкостью
EP3036283B1 (de)	2013-08-21	2019-02-27	Borealis AG	Polyolefinzusammensetzung mit hohem durchfluss mit hoher steifigkeit und zähigkeit
ES2587781T3 (es)	2013-09-27	2016-10-26	Borealis Ag	Películas adecuadas para procesamiento BOPP de polímeros con altos XS y alta Tm
EP2860031B1 (de)	2013-10-11	2016-03-30	Borealis AG	In Maschinenrichtung ausgerichtete Folien für Etiketten
CN104558282B (zh) *	2013-10-18	2017-02-15	中国石油化工股份有限公司	用于烯烃聚合的催化剂组分及其制备方法和用于烯烃聚合的催化剂与应用
US10519259B2 (en)	2013-10-24	2019-12-31	Borealis Ag	Low melting PP homopolymer with high content of regioerrors and high molecular weight
WO2015062787A1 (en)	2013-10-30	2015-05-07	Basell Poliolefine Italia S.R.L.	Multimodal copolymers of propylene and 1-hexene
CA2926061A1 (en)	2013-11-22	2015-05-28	Borealis Ag	Low emission propylene homopolymer
EP3071606B1 (de)	2013-11-22	2017-08-16	Borealis AG	Emissionsarmes propylenhomopolymer mit hohem schmelzfluss
EP3077426B1 (de)	2013-12-04	2022-10-05	Borealis AG	Phthalatfreie pp-homopolymere für schmelzgeblasene fasern
US9637602B2 (en)	2013-12-18	2017-05-02	Borealis Ag	BOPP film with improved stiffness/toughness balance
CN105899599B (zh)	2014-01-15	2018-10-02	埃克森美孚化学专利公司	基于丙烯的抗冲共聚物
US10227427B2 (en)	2014-01-17	2019-03-12	Borealis Ag	Process for preparing propylene/1-butene copolymers
US10100185B2 (en)	2014-02-06	2018-10-16	Borealis Ag	Soft copolymers with high impact strength
PL3102634T3 (pl)	2014-02-06	2020-11-16	Borealis Ag	Miękkie i przezroczyste kopolimery odporne na uderzenia
EP2907841A1 (de)	2014-02-14	2015-08-19	Borealis AG	Polypropylenverbundstoff
CN106232643B (zh)	2014-05-06	2019-02-26	巴塞尔聚烯烃意大利有限公司	无规丙烯-乙烯共聚物及其制备方法
ES2659731T3 (es)	2014-05-20	2018-03-19	Borealis Ag	Composición de polipropileno para aplicaciones en interiores de automóviles
US10550212B2 (en)	2014-09-24	2020-02-04	Basell Poliolefine Italia S.R.L.	Containers comprising propylene-based terpolymers
CN106795347B (zh)	2014-10-01	2018-07-24	巴塞尔聚烯烃意大利有限公司	用于管材的丙烯基共聚物组合物
JP6598285B2 (ja) *	2014-11-11	2019-10-30	サンアロマー株式会社	α−オレフィン類の重合方法
EP3034519B1 (de)	2014-12-17	2018-07-18	Basell Poliolefine Italia S.r.l.	Verbessertes Gasphasenverfahren zur Polymerisierung von Olefinen
WO2016146578A1 (en)	2015-03-19	2016-09-22	Basell Poliolefine Italia S.R.L.	Propylene based terpolymer
WO2016150725A1 (en)	2015-03-24	2016-09-29	Sabic Global Technologies B.V.	Catalyst system and process for the production of polyethylenes.
WO2016188982A1 (en)	2015-05-26	2016-12-01	Basell Poliolefine Italia S.R.L.	Polyolefin gaskets for closures
CN118084613A (zh)	2015-06-01	2024-05-28	Sabic环球技术有限责任公司	用于合成9,9-双(羟甲基)芴的方法
KR101917069B1 (ko)	2015-08-06	2018-11-08	바셀 폴리올레핀 이탈리아 에스.알.엘	프로필렌-에틸렌-1-부텐 터폴리머를 포함하는 조성물
EP3380299B1 (de)	2015-11-24	2019-12-25	Basell Polyolefine GmbH	Polyolefinzusammensetzungen und daraus hergestellte artikel
CN108350234B (zh)	2015-11-24	2019-05-31	巴塞尔聚烯烃股份有限公司	聚烯烃吹塑薄膜
KR102024496B1 (ko)	2015-12-11	2019-09-23	바셀 폴리올레핀 이탈리아 에스.알.엘	프로필렌계 중합체 조성물
EP3387027B1 (de)	2015-12-11	2024-02-14	Basell Poliolefine Italia S.r.l.	Propylen-hexen copolymere
KR101991218B1 (ko)	2016-04-14	2019-09-30	바셀 폴리올레핀 이탈리아 에스.알.엘	프로필렌 중합체 조성물
EP3464458B1 (de)	2016-05-25	2023-11-22	Basell Poliolefine Italia S.r.l.	Folie mit einer polyolefinzusammensetzung
WO2017202597A1 (en)	2016-05-25	2017-11-30	Basell Poliolefine Italia S.R.L.	Film for stretch hood applications
BR112019000684B1 (pt)	2016-07-18	2022-08-30	Equistar Chemicals, Lp	Composição compatibilizante, composição de poliolefina termoplástica, método de fabricação de uma peça moldada por injeção, e artigo
WO2018054362A1 (zh)	2016-09-23	2018-03-29	中国石油化工股份有限公司	用于烯烃聚合的催化剂组分、催化剂及其应用
FI3517553T3 (fi)	2016-09-23	2024-02-02	China Petroleum & Chem Corp	Katalyyttikomponentti käytettäväksi olefiinin polymeroinnissa, katalyytti, ja niiden käyttö
WO2018067367A1 (en)	2016-10-06	2018-04-12	W.R. Grace & Co.-Conn.	Procatalyst composition made with a combination of internal electron donors
US10501616B2 (en)	2016-10-06	2019-12-10	Basell Poliolefine Italia S.R.L.	Propylene-based composition for pipes
EP3526286B1 (de)	2016-10-14	2020-08-19	Basell Poliolefine Italia S.r.l.	Nukleierte propylenpolymerzusammensetzung
PL3545037T3 (pl)	2016-11-23	2021-01-25	Basell Poliolefine Italia S.R.L.	Kompozycja napełnionej poliolefiny
JP7004499B2 (ja)	2016-12-20	2022-01-21	サンアロマー株式会社	マスターバッチ組成物
JP6705949B2 (ja)	2016-12-22	2020-06-03	バーゼル・ポリオレフィン・ゲーエムベーハー	マルチゾーン循環反応器の起動方法
US11453767B2 (en)	2017-03-27	2022-09-27	Basell Poliolefine Italia S.R.L.	Propylene ethylene random copolymer
KR20190125496A (ko)	2017-03-27	2019-11-06	바셀 폴리올레핀 이탈리아 에스.알.엘	올레핀의 기상 중합을 위한 공정
KR102134550B1 (ko)	2017-05-04	2020-07-16	바셀 폴리올레핀 이탈리아 에스.알.엘	프로필렌계 중합체 조성물
US10882287B2 (en)	2017-05-23	2021-01-05	Basell Poliolefine Italia S.R.L.	Multilayer film comprising a polyolefin composition
EP3649192B1 (de)	2017-07-07	2023-11-22	Basell Poliolefine Italia S.r.l.	Polyolefinzusammensetzung für fasern
US11149101B2 (en)	2017-07-19	2021-10-19	Basell Poliolefine Italia S.R.L.	Propylene copolymers
WO2019052822A1 (en)	2017-09-14	2019-03-21	Basell Poliolefine Italia S.R.L.	STATISTIC COPOLYMER OF PROPYLENE AND ETHYLENE
AR112897A1 (es)	2017-09-21	2019-12-26	Basell Poliolefine Italia Srl	Proceso para la polimerización de olefinas en fase gaseosa
WO2019091841A1 (en)	2017-11-09	2019-05-16	Basell Poliolefine Italia S.R.L.	Heat-shrinkable label
US11174379B2 (en)	2017-11-13	2021-11-16	Basell Poliolefine Italia S.R.L.	Compositions obtained from recycled polyolefins
CN111512399B (zh)	2018-02-02	2021-03-19	巴塞尔聚烯烃意大利有限公司	用于电缆绝缘的聚烯烃组合物
WO2019166223A1 (en)	2018-02-28	2019-09-06	Basell Poliolefine Italia S.R.L.	Permeable polymer film
JP7096681B2 (ja)	2018-03-16	2022-07-06	サンアロマー株式会社	ポリプロピレン組成物および成形品
JP7096682B2 (ja)	2018-03-16	2022-07-06	サンアロマー株式会社	ポリプロピレン組成物および成形品
CN111886288A (zh)	2018-04-03	2020-11-03	伊奎斯塔化学有限公司	含液体的聚烯烃母料和方法
JP7153464B2 (ja)	2018-04-27	2022-10-14	サンアロマー株式会社	ポリプロピレン組成物および成形体
JP7114361B2 (ja)	2018-06-19	2022-08-08	サンアロマー株式会社	ポリプロピレン組成物および成形品
BR112021002956A2 (pt)	2018-09-20	2021-05-11	Basell Poliolefine Italia S.R.L.	terpolímero de propileno
WO2020069828A1 (en)	2018-10-03	2020-04-09	Basell Poliolefine Italia S.R.L.	Pipes and polypropylene composition for the manufacture thereof
JP7249126B2 (ja)	2018-10-18	2023-03-30	サンアロマー株式会社	ポリプロピレン組成物および成形品
CN113015624A (zh)	2018-12-05	2021-06-22	巴塞尔聚烯烃意大利有限公司	Bopp多层膜
CN113166551B (zh)	2019-01-10	2023-04-04	巴塞尔聚烯烃意大利有限公司	沥青和聚合物组合物的混合物
EP3911700B1 (de)	2019-01-14	2023-02-15	Basell Poliolefine Italia S.r.l.	Polyolefinzusammensetzung
EP3911702B1 (de)	2019-01-14	2022-12-28	Basell Poliolefine Italia S.r.l.	Polyolefinzusammensetzung
CN113423780B (zh)	2019-03-12	2022-04-19	巴塞尔聚烯烃意大利有限公司	由回收的聚烯烃获得的组合物
US12024623B2 (en)	2019-03-12	2024-07-02	Basell Poliolefine Italia S.R.L.	Compositions obtained from recycled polyolefins
CN113874560B (zh)	2019-06-11	2023-08-08	巴塞尔聚烯烃意大利有限公司	包括丙烯乙烯无规共聚物的纤维
US11814759B2 (en)	2019-06-11	2023-11-14	Basell Poliolefine Italia S.R.L.	Core-skin fiber comprising propylene ethylene random copolymer
EP3766652B1 (de)	2019-07-16	2023-04-12	Basell Poliolefine Italia S.r.l.	Verwendung von spritzgegossenem behälter für mikrowellen
US20220348751A1 (en)	2019-09-12	2022-11-03	Basell Poliolefine Italia S.R.L.	Scratch resistant polyolefin composition
EP4031588B1 (de)	2019-09-17	2023-09-20	Basell Poliolefine Italia S.r.l.	Katalysatorkomponenten zur polymerisierung von olefinen
JP2021066825A (ja)	2019-10-24	2021-04-30	サンアロマー株式会社	ポリプロピレン組成物および成形体
US20230075830A1 (en)	2019-12-03	2023-03-09	Basell Polyolefine Gmbh	Polyethylene composition for filaments or fibers
BR112022008804A2 (pt)	2019-12-03	2022-07-26	Basell Polyolefine Gmbh	Composição de polietileno, filamento ou fibra, e, itens fabricados
EP4069754A1 (de)	2019-12-04	2022-10-12	Basell Poliolefine Italia S.r.l.	Katalysator zur polymerisation von olefinen
EP4114872A1 (de)	2020-03-04	2023-01-11	Basell Poliolefine Italia S.r.l.	Copolymer auf propylenbasis für behälter
EP4127055A1 (de)	2020-03-30	2023-02-08	Basell Poliolefine Italia S.r.l.	Propylenpolymerzusammensetzung
MX2022012614A (es)	2020-04-21	2022-11-07	Basell Poliolefine Italia Srl	Material de asfalto mejorado.
EP4139398A1 (de)	2020-04-21	2023-03-01	Basell Poliolefine Italia S.r.l.	Mischungen aus bitumen- und polymerzusammensetzungen
CN115397922A (zh)	2020-04-21	2022-11-25	巴塞尔聚烯烃意大利有限公司	改进的沥青质材料
MX2022012617A (es) *	2020-04-21	2022-11-07	Basell Poliolefine Italia Srl	Mezclas de composiciones de bitumen y composiciones polimericas.
WO2021233875A1 (en)	2020-05-22	2021-11-25	Basell Poliolefine Italia S.R.L.	Highly filled and flexible polyolefin composition
JP7389281B2 (ja)	2020-06-30	2023-11-29	バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ	ポリプロピレン組成物
US20230265272A1 (en)	2020-07-21	2023-08-24	Basell Poliolefine Italia S.R.L.	High flow heterophasic polypropylene as appearance improver in polyolefin compositions
CN115996844A (zh)	2020-07-24	2023-04-21	巴塞尔聚烯烃意大利有限公司	用于屋顶应用的聚烯烃组合物
EP4192688A1 (de)	2020-08-07	2023-06-14	Basell Poliolefine Italia S.r.l.	Weiche und flexible polyolefinzusammensetzung
CN116209686B (zh)	2020-10-19	2024-01-26	巴塞尔聚烯烃意大利有限公司	聚丙烯组合物
US20240124693A1 (en)	2020-12-09	2024-04-18	Basell Poliolefine Italia S.R.L.	Propylene polymer composition
US20240059885A1 (en)	2020-12-14	2024-02-22	Basell Poliolefine Italia S.R.L.	Ultrasoft polyolefin composition
CN116670228A (zh)	2020-12-15	2023-08-29	巴塞尔聚烯烃意大利有限公司	具有高透明度的聚烯烃组合物
CN114763425B (zh) *	2021-01-12	2024-03-01	中国石油天然气股份有限公司	Bopp聚丙烯专用料以及无“白点”bopp薄膜
WO2022167182A1 (en)	2021-02-08	2022-08-11	Basell Poliolefine Italia S.R.L.	Polyolefin composition for functional films
CN116761721A (zh)	2021-02-26	2023-09-15	巴塞尔聚烯烃股份有限公司	用于挤出增材制造的印刷平台
US20240218091A1 (en)	2021-04-06	2024-07-04	Basell Poliolefine Italia S.R.L.	Pre-polymerized catalyst components for the polymerization of olefins
EP4323448A1 (de)	2021-04-14	2024-02-21	Basell Poliolefine Italia S.r.l.	Propylenpolymerzusammensetzungen
JP2024519028A (ja)	2021-06-10	2024-05-08	バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ	ポリプロピレン組成物およびそれで製造された光源用カバー
WO2022263212A1 (en)	2021-06-16	2022-12-22	Basell Poliolefine Italia S.R.L.	Filled polyolefin composition
CN117730120A (zh)	2021-06-25	2024-03-19	巴塞尔聚烯烃意大利有限公司	聚丙烯基树脂组合物、片材模塑品和容器
CN117693556A (zh)	2021-06-25	2024-03-12	巴塞尔聚烯烃意大利有限公司	聚丙烯基树脂组合物及其制备方法、膜模制品、与食品接触的包装、与食品接触的容器和蒸煮袋
JPWO2022270630A1 (de)	2021-06-25	2022-12-29
WO2023285114A1 (en)	2021-07-12	2023-01-19	Basell Poliolefine Italia S.R.L.	Filled polyolefin composition
WO2023025622A1 (en)	2021-08-24	2023-03-02	Basell Poliolefine Italia S.R.L.	Propylene ethylene copolymer
WO2023057054A1 (en)	2021-10-06	2023-04-13	Basell Poliolefine Italia S.R.L.	Polypropylene composition
CN118055858A (zh)	2021-10-28	2024-05-17	巴塞尔聚烯烃股份有限公司	增强聚丙烯组合物
WO2023104696A1 (en)	2021-12-10	2023-06-15	Basell Poliolefine Italia S.R.L.	Polyolefin filament
WO2023104697A1 (en)	2021-12-10	2023-06-15	Basell Poliolefine Italia S.R.L.	Polyolefin filament
CN118234796A (zh)	2021-12-14	2024-06-21	巴塞尔聚烯烃意大利有限公司	丙烯基聚合物组合物
WO2023117512A1 (en)	2021-12-23	2023-06-29	Basell Poliolefine Italia S.R.L.	Soft polyolefin composition
WO2023156103A1 (en)	2022-02-17	2023-08-24	Basell Poliolefine Italia S.R.L.	Pipes and polypropylene composition for the manufacture thereof
WO2023198642A1 (en)	2022-04-12	2023-10-19	Basell Poliolefine Italia S.R.L.	Propylene-based copolymer composition
WO2023198643A1 (en)	2022-04-12	2023-10-19	Basell Poliolefine Italia S.R.L.	Propylene-based copolymer compositon
WO2023213536A1 (en)	2022-05-06	2023-11-09	Basell Poliolefine Italia S.R.L.	Plastic material and shaped article obtained therefrom
WO2023237374A1 (en)	2022-06-06	2023-12-14	Basell Poliolefine Italia S.R.L.	Propylene-based copolymer compositon
WO2023237341A1 (en)	2022-06-06	2023-12-14	Basell Poliolefine Italia S.R.L.	Propylene-based copolymer compositon
WO2023247227A1 (en)	2022-06-20	2023-12-28	Basell Poliolefine Italia S.R.L.	Multilayer film
WO2024028042A1 (en)	2022-08-03	2024-02-08	Basell Poliolefine Italia S.R.L.	Polypropylene composition for heat sealable films
WO2024083610A1 (en)	2022-10-20	2024-04-25	Basell Poliolefine Italia S.R.L.	Polypropylene composition with good sealing properties
WO2024099644A1 (en)	2022-11-07	2024-05-16	Basell Poliolefine Italia S.R.L.	Molded article comprising propylene homopolymer
WO2024099643A1 (en)	2022-11-07	2024-05-16	Basell Poliolefine Italia S.R.L.	Molded article comprising a propylene homopolymer composition
WO2024099626A1 (en)	2022-11-07	2024-05-16	Basell Poliolefine Italia S.R.L.	Propylene homopolymer
WO2024099628A1 (en)	2022-11-07	2024-05-16	Basell Poliolefine Italia S.R.L.	Propylene homopolymer
EP4372016A1 (de)	2022-11-18	2024-05-22	Basell Poliolefine Italia S.r.l.	Olefinpolymerisationsverfahren unter verwendung einer antistatischen zusammensetzung
WO2024132732A1 (en)	2022-12-19	2024-06-27	Basell Poliolefine Italia S.R.L.	Colored thermoplastic composition

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
IT1227259B (it) *	1988-09-30	1991-03-28	Himont Inc	Catalizzatori per la polimerizzazione di olefine.
IT1237812B (it) *	1989-12-22	1993-06-17	Himont Inc	Componenti e catalizzatori per la polimerizzazione di olefine
IT1241093B (it) *	1990-03-30	1993-12-29	Himont Inc	Componenti e catalizzatori per la polimerizzazione di olefine
EP0452156B1 (de) *	1990-04-13	1997-08-13	Mitsui Petrochemical Industries, Ltd.	Festes Titan enthaltendes Katalysatorbestandteil und Katalysator für Olefinpolymerisation, vorpolymerisierte Olefinpolymerisationskatalysator und Verfahren für Olefinpolymerisation

1996
- 1996-02-12 IL IL11711496A patent/IL117114A/xx not_active IP Right Cessation
- 1996-02-13 MY MYPI96000538A patent/MY115716A/en unknown
- 1996-02-13 CA CA002169401A patent/CA2169401C/en not_active Expired - Fee Related
- 1996-02-16 AU AU45594/96A patent/AU699522B2/en not_active Ceased
- 1996-02-16 BR BR9600767A patent/BR9600767A/pt not_active IP Right Cessation
- 1996-02-18 CN CN96107325A patent/CN1090194C/zh not_active Expired - Fee Related
- 1996-02-20 IN IN316CA1996 patent/IN186169B/en unknown
- 1996-02-20 HU HU9600390A patent/HU221228B1/hu not_active IP Right Cessation
- 1996-02-20 UA UA96020629A patent/UA60290C2/uk unknown
- 1996-02-20 RU RU96103154/04A patent/RU2156260C2/ru active
- 1996-02-20 NO NO960669A patent/NO309380B1/no not_active IP Right Cessation
- 1996-02-21 AR ARP960101455A patent/AR000994A1/es unknown
- 1996-02-21 DE DE69600532T patent/DE69600532T2/de not_active Expired - Lifetime
- 1996-02-21 FI FI960786A patent/FI119643B/fi not_active IP Right Cessation
- 1996-02-21 JP JP03409196A patent/JP3904117B2/ja not_active Expired - Fee Related
- 1996-02-21 ES ES96102584T patent/ES2121446T3/es not_active Expired - Lifetime
- 1996-02-21 AT AT96102584T patent/ATE169937T1/de active
- 1996-02-21 EP EP96102584A patent/EP0728769B1/de not_active Expired - Lifetime
- 1996-02-21 KR KR1019960004091A patent/KR100424925B1/ko not_active IP Right Cessation
1998
- 1998-09-29 HK HK98111070A patent/HK1010379A1/xx not_active IP Right Cessation

Also Published As

Publication number	Publication date
EP0728769B1 (de)	1998-08-19
IN186169B (de)	2001-06-30
AU699522B2 (en)	1998-12-03
CN1143651A (zh)	1997-02-26
IL117114A0 (en)	1996-07-23
DE69600532D1 (de)	1998-09-24
CA2169401A1 (en)	1996-08-22
MX9600627A (es)	1997-07-31
RU2156260C2 (ru)	2000-09-20
HUP9600390A2 (en)	1997-04-28
NO960669D0 (no)	1996-02-20
KR960031489A (ko)	1996-09-17
MY115716A (en)	2003-08-30
HUP9600390A3 (en)	2000-03-28
AR000994A1 (es)	1997-08-27
BR9600767A (pt)	1997-12-23
AU4559496A (en)	1996-08-29
FI960786A (fi)	1996-08-22
CN1090194C (zh)	2002-09-04
HU221228B1 (en)	2002-08-28
IL117114A (en)	2000-02-17
HK1010379A1 (en)	1999-06-17
FI960786A0 (fi)	1996-02-21
UA60290C2 (uk)	2003-10-15
JP3904117B2 (ja)	2007-04-11
JPH0920803A (ja)	1997-01-21
KR100424925B1 (ko)	2004-06-26
NO960669L (no)	1996-08-22
HU9600390D0 (en)	1996-04-29
CA2169401C (en)	2007-04-10
EP0728769A1 (de)	1996-08-28
FI119643B (fi)	2009-01-30
ES2121446T3 (es)	1998-11-16
DE69600532T2 (de)	1999-03-18
ATE169937T1 (de)	1998-09-15

Legal Events

Date	Code	Title	Description
2010-09-27	MM1K	Lapsed by not paying the annual fees

Publication	Publication Date	Title
NO309380B1 (no)	2001-01-22	Katalysatorbestanddel og katalysatorer for polymerisering av olefiner, samt fremgangsmåte for polymerisering av olefiner
US7022640B2 (en)	2006-04-04	1,3-diethers and components and catalysts for the polymerization of olefins, containing said diethers
EP0728770B1 (de)	1999-07-14	Verfahren zur Herstellung von festen Katalysatorkomponenten für die Olefinpolymerisation
JP6130436B2 (ja)	2017-05-17	オレフィン重合用触媒組成物
AU759295B2 (en)	2003-04-10	Catalyst components for the polymerization of olefins
EP0361494B1 (de)	1996-02-07	Bestandteil und Katalysator für Olefinpolymerisation
FI95277B (fi)	1995-09-29	Olefiinien polymeroinnissa käytettäviä katalysaattoreita
JP2003522231A (ja)	2003-07-22	オレフィン重合用成分及び触媒
NO301123B1 (no)	1997-09-15	Fremgangsmåte for fremstilling av stabiliserte polyolefiner
EP1483301B1 (de)	2009-02-18	Verfahren zur herstellung einer katalysatorkomponente basierend auf einem diether
JP2002173504A (ja)	2002-06-21	オレフィン重合用触媒およびオレフィン重合方法
US9777084B2 (en)	2017-10-03	Catalyst system for olefin polymerization and method for producing olefin polymer
US20050187359A1 (en)	2005-08-25	Solid catalyst component for olefin polymerization, catalyst for olefin polymerization and method for producing olefin polymer
US7081427B2 (en)	2006-07-25	Solid catalyst component for olefin polymerization
JP5129540B2 (ja)	2013-01-30	α−オレフィン重合体及びその製造方法
MXPA96000627A (en)	1997-12-01	Components and catalysts for olefi polymerization
JP2001139618A (ja)	2001-05-22	オレフィン重合用固体触媒成分、オレフィン重合用触媒及びオレフィン重合体の製造方法
ITMI950318A1 (it)	1996-08-21	Catalizzatori per la polimerizzazione delle olefine