FR2639351A1 - - Google Patents
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- Publication number
- FR2639351A1 FR2639351A1 FR8815261A FR8815261A FR2639351A1 FR 2639351 A1 FR2639351 A1 FR 2639351A1 FR 8815261 A FR8815261 A FR 8815261A FR 8815261 A FR8815261 A FR 8815261A FR 2639351 A1 FR2639351 A1 FR 2639351A1
- Authority
- FR
- France
- Prior art keywords
- titanium
- metal
- products
- reduction
- treatment
- 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.)
- Granted
Links
- 230000003197 catalytic effect Effects 0.000 claims abstract description 23
- 238000000034 method Methods 0.000 claims abstract description 23
- 239000010936 titanium Substances 0.000 claims abstract description 23
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 20
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 19
- 239000005977 Ethylene Substances 0.000 claims abstract description 19
- 150000001875 compounds Chemical class 0.000 claims abstract description 19
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000000460 chlorine Substances 0.000 claims abstract description 10
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 8
- 239000011777 magnesium Substances 0.000 claims abstract description 8
- 239000003054 catalyst Substances 0.000 claims abstract description 7
- 229910052749 magnesium Inorganic materials 0.000 claims abstract description 7
- 239000000725 suspension Substances 0.000 claims abstract description 7
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910052723 transition metal Inorganic materials 0.000 claims abstract description 5
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims abstract description 4
- 230000003647 oxidation Effects 0.000 claims abstract description 4
- 238000007254 oxidation reaction Methods 0.000 claims abstract description 4
- 150000003624 transition metals Chemical class 0.000 claims abstract description 4
- 239000004711 α-olefin Substances 0.000 claims abstract description 4
- 239000003638 chemical reducing agent Substances 0.000 claims description 9
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 239000002184 metal Substances 0.000 claims description 9
- 238000006116 polymerization reaction Methods 0.000 claims description 9
- 229930195733 hydrocarbon Natural products 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 150000002736 metal compounds Chemical group 0.000 claims description 6
- 239000004215 Carbon black (E152) Substances 0.000 claims description 5
- 150000002430 hydrocarbons Chemical class 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- 150000003623 transition metal compounds Chemical class 0.000 claims description 5
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 150000001805 chlorine compounds Chemical class 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 230000000737 periodic effect Effects 0.000 claims description 2
- 238000007334 copolymerization reaction Methods 0.000 claims 1
- 229920000642 polymer Polymers 0.000 description 16
- 238000009826 distribution Methods 0.000 description 13
- -1 polyethylene Polymers 0.000 description 12
- 238000006722 reduction reaction Methods 0.000 description 8
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 6
- 239000000203 mixture Substances 0.000 description 5
- 229910052782 aluminium Inorganic materials 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000000155 melt Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 125000005234 alkyl aluminium group Chemical group 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 150000004678 hydrides Chemical class 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- QQRSPHJOOXUALR-UHFFFAOYSA-N Apiole Chemical compound COC1=CC(CC=C)=C(OC)C2=C1OCO2 QQRSPHJOOXUALR-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical group 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 239000003085 diluting agent 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
- 238000012685 gas phase polymerization Methods 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 235000001055 magnesium Nutrition 0.000 description 2
- 150000002681 magnesium compounds Chemical class 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 150000004756 silanes Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 150000003609 titanium compounds Chemical class 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- VFWCMGCRMGJXDK-UHFFFAOYSA-N 1-chlorobutane Chemical compound CCCCCl VFWCMGCRMGJXDK-UHFFFAOYSA-N 0.000 description 1
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 1
- 101710179734 6,7-dimethyl-8-ribityllumazine synthase 2 Proteins 0.000 description 1
- 101150067361 Aars1 gene Proteins 0.000 description 1
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- 229910001148 Al-Li alloy Inorganic materials 0.000 description 1
- 241000913828 Apios Species 0.000 description 1
- 101100496169 Arabidopsis thaliana CLH1 gene Proteins 0.000 description 1
- 241001133287 Artocarpus hirsutus Species 0.000 description 1
- 229910015900 BF3 Inorganic materials 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- 101100379317 Butyrivibrio fibrisolvens apt gene Proteins 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- FHUODBDRWMIBQP-UHFFFAOYSA-N Ethyl p-anisate Chemical compound CCOC(=O)C1=CC=C(OC)C=C1 FHUODBDRWMIBQP-UHFFFAOYSA-N 0.000 description 1
- 239000013032 Hydrocarbon resin Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 101710186609 Lipoyl synthase 2 Proteins 0.000 description 1
- 101710122908 Lipoyl synthase 2, chloroplastic Proteins 0.000 description 1
- 101710101072 Lipoyl synthase 2, mitochondrial Proteins 0.000 description 1
- 101100044057 Mesocricetus auratus SYCP3 gene Proteins 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 101100080600 Schizosaccharomyces pombe (strain 972 / ATCC 24843) nse6 gene Proteins 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- 229910003074 TiCl4 Inorganic materials 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000011954 Ziegler–Natta catalyst Substances 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- JFBZPFYRPYOZCQ-UHFFFAOYSA-N [Li].[Al] Chemical compound [Li].[Al] JFBZPFYRPYOZCQ-UHFFFAOYSA-N 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 229940037003 alum Drugs 0.000 description 1
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical class Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 1
- 101150033016 aptA gene Proteins 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- 238000000071 blow moulding Methods 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000012320 chlorinating reagent Substances 0.000 description 1
- 238000005660 chlorination reaction Methods 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 101150111293 cor-1 gene Proteins 0.000 description 1
- 150000004292 cyclic ethers Chemical class 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000010101 extrusion blow moulding Methods 0.000 description 1
- 239000007792 gaseous phase Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 229920006270 hydrocarbon resin Polymers 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000007517 lewis acids Chemical group 0.000 description 1
- 150000002680 magnesium Chemical class 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- QSSJZLPUHJDYKF-UHFFFAOYSA-N methyl 4-methylbenzoate Chemical compound COC(=O)C1=CC=C(C)C=C1 QSSJZLPUHJDYKF-UHFFFAOYSA-N 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- UGNWTBMOAKPKBL-UHFFFAOYSA-N tetrachloro-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(Cl)=C(Cl)C1=O UGNWTBMOAKPKBL-UHFFFAOYSA-N 0.000 description 1
- 150000003608 titanium Chemical class 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
- CMWCOKOTCLFJOP-UHFFFAOYSA-N titanium(3+) Chemical compound [Ti+3] CMWCOKOTCLFJOP-UHFFFAOYSA-N 0.000 description 1
- JCVQKRGIASEUKR-UHFFFAOYSA-N triethoxy(phenyl)silane Chemical compound CCO[Si](OCC)(OCC)C1=CC=CC=C1 JCVQKRGIASEUKR-UHFFFAOYSA-N 0.000 description 1
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229910052726 zirconium Inorganic materials 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
- C08F10/02—Ethene
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Separation, Recovery Or Treatment Of Waste Materials Containing Plastics (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Polyethers (AREA)
- Polymerisation Methods In General (AREA)
Priority Applications (12)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8815261A FR2639351B1 (OSRAM) | 1988-11-23 | 1988-11-23 | |
| US07/436,059 US5151396A (en) | 1988-11-23 | 1989-11-13 | Process for the polymerization of ethylene and catalytic component therefor |
| NO894514A NO174714C (no) | 1988-11-23 | 1989-11-13 | Fremgangsmåte for polymerisering av etylen for å oppnå en polymer med bred molekylvektsfordeling |
| DE89403126T DE68906766T2 (de) | 1988-11-23 | 1989-11-14 | Verfahren für die Ethylenpolymerisation zur Herstellung von Polyethylen mit breiter Molekulargewichtsverteilung, Verfahren zur Behandlung des Katalysatorbestandteils. |
| ES89403126T ES2045512T3 (es) | 1988-11-23 | 1989-11-14 | Procedimiento de polimerizacion del etileno que permite obtener un polimero de amplia distribucion de masas moleculares, procedimiento de tratamiento del componente catalitico. |
| EP89403126A EP0370864B1 (fr) | 1988-11-23 | 1989-11-14 | Procédé de polymérisation de l'éthylène permettant d'obtenir un polymère de distribution large de masses moleculaires, procédé de traitement de la composante catalytique |
| AT89403126T ATE89832T1 (de) | 1988-11-23 | 1989-11-14 | Verfahren fuer die ethylenpolymerisation zur herstellung von polyethylen mit breiter molekulargewichtsverteilung, verfahren zur behandlung des katalysatorbestandteils. |
| CA002003055A CA2003055C (fr) | 1988-11-23 | 1989-11-15 | Procede de polymerisation de l'ethylene permettant d'obtenir un polymere de distribution large de masses moleculaires |
| FI895586A FI96769C (fi) | 1988-11-23 | 1989-11-22 | Etyleenin polymerointimenetelmä, jonka avulla on mahdollista saada molekyylimassajakaumaltaan laaja polymeeri. Katalyyttisen komponentin käsittelymenetelmä |
| JP1304543A JP2813392B2 (ja) | 1988-11-23 | 1989-11-22 | エチレンの重合方法及び使用する触媒成分 |
| CN89108760A CN1039127C (zh) | 1988-11-23 | 1989-11-23 | 一种催化乙烯聚合或乙烯与α-烯烃共聚合的方法 |
| US08/320,053 US5563225A (en) | 1988-11-23 | 1994-10-07 | Process for the polymerization of ethylene and catalytic component therefor |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8815261A FR2639351B1 (OSRAM) | 1988-11-23 | 1988-11-23 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| FR2639351A1 true FR2639351A1 (OSRAM) | 1990-05-25 |
| FR2639351B1 FR2639351B1 (OSRAM) | 1992-12-31 |
Family
ID=9372150
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FR8815261A Expired - Lifetime FR2639351B1 (OSRAM) | 1988-11-23 | 1988-11-23 |
Country Status (11)
| Country | Link |
|---|---|
| US (2) | US5151396A (OSRAM) |
| EP (1) | EP0370864B1 (OSRAM) |
| JP (1) | JP2813392B2 (OSRAM) |
| CN (1) | CN1039127C (OSRAM) |
| AT (1) | ATE89832T1 (OSRAM) |
| CA (1) | CA2003055C (OSRAM) |
| DE (1) | DE68906766T2 (OSRAM) |
| ES (1) | ES2045512T3 (OSRAM) |
| FI (1) | FI96769C (OSRAM) |
| FR (1) | FR2639351B1 (OSRAM) |
| NO (1) | NO174714C (OSRAM) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2686609B1 (fr) * | 1992-01-27 | 1995-06-16 | Atochem Elf Sa | Procede de polymerisation de l'ethylene permettant d'obtenir un polymere de distribution large de masses moleculaires. procede de traitement de la composante catalytique. |
| US5235011A (en) * | 1992-08-31 | 1993-08-10 | Phillips Petroleum Company | Polyolefin polymerization process, method of producing catalyst, and catalyst |
| WO1998033823A1 (en) * | 1997-02-05 | 1998-08-06 | The Penn State Research Foundation | METAL CATALYZED SYNTHESIS OF HYPERBRANCHED ETHYLENE AND/OR α-OLEFIN POLYMERS |
| FR2769521B1 (fr) * | 1997-10-14 | 1999-12-10 | Rhodia Chimie Sa | Composition a base d'un oxyde metallique greffe, sa preparation et son utilisation dans un procede de polymerisation par ouverture de cycles oxygenes |
| US20050085601A1 (en) * | 2003-10-15 | 2005-04-21 | Kayo Vizzini | Process for forming Ziegler-Natta catalyst for use in polyolefin production |
| JP5695869B2 (ja) * | 2010-09-28 | 2015-04-08 | 日本ポリエチレン株式会社 | チーグラー・ナッタ触媒の改質方法および改質されたチーグラー・ナッタ触媒、並びにそれを用いたオレフィンの重合方法および得られたオレフィン系重合体 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0060443A1 (en) * | 1981-03-04 | 1982-09-22 | Phillips Petroleum Company | Catalyst and use of same for polymerization |
| EP0101978A1 (en) * | 1982-08-05 | 1984-03-07 | Phillips Petroleum Company | Olefin polymerization |
| EP0143002A1 (en) * | 1983-11-23 | 1985-05-29 | BP Chemicals Limited | Catalyst and process for polymerising olefins |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL162664B (nl) * | 1969-06-20 | 1980-01-15 | Montedison Spa | Werkwijze om een katalysator te bereiden voor de poly- merisatie van alkenen-1. |
| JPS5846125B2 (ja) * | 1976-10-06 | 1983-10-14 | 旭化成株式会社 | オレフイン重合触媒 |
| JPS5846202B2 (ja) * | 1979-01-31 | 1983-10-14 | 住友化学工業株式会社 | オレフィン重合体の製造法 |
| US4410672A (en) * | 1980-04-23 | 1983-10-18 | Showa Denko Kabushiki Kaisha | Polymerization catalysts and process for the production of ethylenic polymers by use thereof |
| US4536487A (en) * | 1980-11-24 | 1985-08-20 | National Distillers And Chemical Corporation | Intermetallic compounds of polymeric transition metal oxide alkoxides and catalytic use thereof |
| US4525554A (en) * | 1981-03-04 | 1985-06-25 | Mitsubishi Chemical Industries Ltd. | Process for polymerizing olefin |
| JPS5853905A (ja) * | 1981-09-29 | 1983-03-30 | Toa Nenryo Kogyo Kk | オレフイン重合用触媒成分 |
| JPH0674292B2 (ja) * | 1984-11-30 | 1994-09-21 | 東燃株式会社 | エチレン重合用触媒成分の製造法 |
| US4698323A (en) * | 1986-09-29 | 1987-10-06 | Stauffer Chemical Company | Transition metal catalyst component containing magnesium alkoxy alkoxides |
-
1988
- 1988-11-23 FR FR8815261A patent/FR2639351B1/fr not_active Expired - Lifetime
-
1989
- 1989-11-13 US US07/436,059 patent/US5151396A/en not_active Expired - Fee Related
- 1989-11-13 NO NO894514A patent/NO174714C/no not_active IP Right Cessation
- 1989-11-14 DE DE89403126T patent/DE68906766T2/de not_active Expired - Fee Related
- 1989-11-14 AT AT89403126T patent/ATE89832T1/de not_active IP Right Cessation
- 1989-11-14 ES ES89403126T patent/ES2045512T3/es not_active Expired - Lifetime
- 1989-11-14 EP EP89403126A patent/EP0370864B1/fr not_active Expired - Lifetime
- 1989-11-15 CA CA002003055A patent/CA2003055C/fr not_active Expired - Fee Related
- 1989-11-22 FI FI895586A patent/FI96769C/fi not_active IP Right Cessation
- 1989-11-22 JP JP1304543A patent/JP2813392B2/ja not_active Expired - Lifetime
- 1989-11-23 CN CN89108760A patent/CN1039127C/zh not_active Expired - Fee Related
-
1994
- 1994-10-07 US US08/320,053 patent/US5563225A/en not_active Expired - Fee Related
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0060443A1 (en) * | 1981-03-04 | 1982-09-22 | Phillips Petroleum Company | Catalyst and use of same for polymerization |
| EP0101978A1 (en) * | 1982-08-05 | 1984-03-07 | Phillips Petroleum Company | Olefin polymerization |
| EP0143002A1 (en) * | 1983-11-23 | 1985-05-29 | BP Chemicals Limited | Catalyst and process for polymerising olefins |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0370864B1 (fr) | 1993-05-26 |
| FI96769B (fi) | 1996-05-15 |
| US5563225A (en) | 1996-10-08 |
| ATE89832T1 (de) | 1993-06-15 |
| NO894514D0 (no) | 1989-11-13 |
| CA2003055C (fr) | 2000-01-11 |
| CN1042919A (zh) | 1990-06-13 |
| ES2045512T3 (es) | 1994-01-16 |
| FI895586A0 (fi) | 1989-11-22 |
| DE68906766D1 (de) | 1993-07-01 |
| DE68906766T2 (de) | 1993-10-21 |
| EP0370864A1 (fr) | 1990-05-30 |
| CN1039127C (zh) | 1998-07-15 |
| NO894514L (no) | 1990-05-25 |
| CA2003055A1 (fr) | 1990-05-23 |
| FI96769C (fi) | 1996-08-26 |
| NO174714B (no) | 1994-03-14 |
| FR2639351B1 (OSRAM) | 1992-12-31 |
| NO174714C (no) | 1994-06-22 |
| JPH02185507A (ja) | 1990-07-19 |
| US5151396A (en) | 1992-09-29 |
| JP2813392B2 (ja) | 1998-10-22 |
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