PL83672B1 - - Google Patents
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- Publication number
- PL83672B1 PL83672B1 PL1972156223A PL15622372A PL83672B1 PL 83672 B1 PL83672 B1 PL 83672B1 PL 1972156223 A PL1972156223 A PL 1972156223A PL 15622372 A PL15622372 A PL 15622372A PL 83672 B1 PL83672 B1 PL 83672B1
- Authority
- PL
- Poland
- Prior art keywords
- compound
- anhydrous
- polymer
- heptane
- titanium
- Prior art date
Links
- 239000010936 titanium Substances 0.000 claims description 76
- 238000006116 polymerization reaction Methods 0.000 claims description 50
- 239000003054 catalyst Substances 0.000 claims description 45
- 150000001875 compounds Chemical class 0.000 claims description 36
- 239000000203 mixture Substances 0.000 claims description 36
- 238000000034 method Methods 0.000 claims description 33
- -1 alkylaluminum compound Chemical class 0.000 claims description 26
- 229910052719 titanium Inorganic materials 0.000 claims description 25
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 23
- 239000000047 product Substances 0.000 claims description 22
- 229910052749 magnesium Inorganic materials 0.000 claims description 15
- 239000011777 magnesium Substances 0.000 claims description 15
- 239000004711 α-olefin Substances 0.000 claims description 12
- 238000002360 preparation method Methods 0.000 claims description 11
- 238000002083 X-ray spectrum Methods 0.000 claims description 10
- 229910052782 aluminium Inorganic materials 0.000 claims description 9
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 8
- 150000003609 titanium compounds Chemical class 0.000 claims description 8
- 150000002148 esters Chemical class 0.000 claims description 7
- 150000004985 diamines Chemical class 0.000 claims description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 5
- 239000005977 Ethylene Substances 0.000 claims description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 5
- 239000007795 chemical reaction product Substances 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- 239000000843 powder Substances 0.000 claims description 5
- 238000006467 substitution reaction Methods 0.000 claims description 5
- 239000002879 Lewis base Substances 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 4
- 150000007527 lewis bases Chemical class 0.000 claims description 4
- 238000007259 addition reaction Methods 0.000 claims description 3
- 150000002680 magnesium Chemical class 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 148
- 229920000642 polymer Polymers 0.000 description 69
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 53
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 46
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 46
- 238000009835 boiling Methods 0.000 description 40
- 238000000605 extraction Methods 0.000 description 40
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 32
- MTZQAGJQAFMTAQ-UHFFFAOYSA-N ethyl benzoate Chemical compound CCOC(=O)C1=CC=CC=C1 MTZQAGJQAFMTAQ-UHFFFAOYSA-N 0.000 description 30
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 26
- 229910001629 magnesium chloride Inorganic materials 0.000 description 26
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical class Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 25
- 229910003074 TiCl4 Inorganic materials 0.000 description 24
- 229910052757 nitrogen Inorganic materials 0.000 description 24
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 17
- 239000000725 suspension Substances 0.000 description 17
- 229910052748 manganese Inorganic materials 0.000 description 16
- 239000011572 manganese Substances 0.000 description 16
- 229910001220 stainless steel Inorganic materials 0.000 description 14
- 239000010935 stainless steel Substances 0.000 description 14
- 229910052786 argon Inorganic materials 0.000 description 13
- 239000004743 Polypropylene Substances 0.000 description 11
- 230000000694 effects Effects 0.000 description 11
- 229920001155 polypropylene Polymers 0.000 description 11
- 239000011521 glass Substances 0.000 description 10
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- 239000012043 crude product Substances 0.000 description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
- 238000000227 grinding Methods 0.000 description 8
- 150000004820 halides Chemical class 0.000 description 8
- 239000002585 base Substances 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 7
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 6
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 6
- 239000002002 slurry Substances 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 229960004132 diethyl ether Drugs 0.000 description 5
- 238000001035 drying Methods 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- CQDGTJPVBWZJAZ-UHFFFAOYSA-N monoethyl carbonate Chemical compound CCOC(O)=O CQDGTJPVBWZJAZ-UHFFFAOYSA-N 0.000 description 4
- AVQQQNCBBIEMEU-UHFFFAOYSA-N 1,1,3,3-tetramethylurea Chemical compound CN(C)C(=O)N(C)C AVQQQNCBBIEMEU-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 229910010062 TiCl3 Inorganic materials 0.000 description 3
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 3
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 3
- 150000002170 ethers Chemical class 0.000 description 3
- 229940052303 ethers for general anesthesia Drugs 0.000 description 3
- 229920001580 isotactic polymer Polymers 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 230000000737 periodic effect Effects 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-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
- ABDKAPXRBAPSQN-UHFFFAOYSA-N veratrole Chemical compound COC1=CC=CC=C1OC ABDKAPXRBAPSQN-UHFFFAOYSA-N 0.000 description 3
- UAIVFDJJMVMUGY-UHFFFAOYSA-N 1,2,4-trimethylpiperazine Chemical compound CC1CN(C)CCN1C UAIVFDJJMVMUGY-UHFFFAOYSA-N 0.000 description 2
- RXYPXQSKLGGKOL-UHFFFAOYSA-N 1,4-dimethylpiperazine Chemical compound CN1CCN(C)CC1 RXYPXQSKLGGKOL-UHFFFAOYSA-N 0.000 description 2
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- OJVAMHKKJGICOG-UHFFFAOYSA-N 2,5-hexanedione Chemical compound CC(=O)CCC(C)=O OJVAMHKKJGICOG-UHFFFAOYSA-N 0.000 description 2
- IEOPZUMPHCZMCS-UHFFFAOYSA-N 2-(methoxymethyl)oxolane Chemical compound COCC1CCCO1 IEOPZUMPHCZMCS-UHFFFAOYSA-N 0.000 description 2
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- FHUODBDRWMIBQP-UHFFFAOYSA-N Ethyl p-anisate Chemical compound CCOC(=O)C1=CC=C(OC)C=C1 FHUODBDRWMIBQP-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 229910052925 anhydrite Inorganic materials 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 239000003701 inert diluent Substances 0.000 description 2
- 239000012442 inert solvent Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000012299 nitrogen atmosphere Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 2
- SKNDLWNTAARIAK-UHFFFAOYSA-N 2-oxo-1,3,2lambda5-dioxaphosphonan-2-amine Chemical compound NP1(=O)OCCCCCCO1 SKNDLWNTAARIAK-UHFFFAOYSA-N 0.000 description 1
- OOMSPUWLXIPBHS-UHFFFAOYSA-N 2-sulfoethanethioic S-acid Chemical compound C(C(=O)S)S(=O)(=O)O OOMSPUWLXIPBHS-UHFFFAOYSA-N 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 244000201986 Cassia tora Species 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 1
- 229910012465 LiTi Inorganic materials 0.000 description 1
- 101100496858 Mus musculus Colec12 gene Proteins 0.000 description 1
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 1
- KIDHWZJUCRJVML-UHFFFAOYSA-N Putrescine Natural products NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- RBFQJDQYXXHULB-UHFFFAOYSA-N arsane Chemical class [AsH3] RBFQJDQYXXHULB-UHFFFAOYSA-N 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 229920001585 atactic polymer Polymers 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- LJSQFQKUNVCTIA-UHFFFAOYSA-N diethyl sulfide Chemical compound CCSCC LJSQFQKUNVCTIA-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000009837 dry grinding Methods 0.000 description 1
- KUGSJJNCCNSRMM-UHFFFAOYSA-N ethoxyboronic acid Chemical compound CCOB(O)O KUGSJJNCCNSRMM-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- UKFXDFUAPNAMPJ-UHFFFAOYSA-N ethylmalonic acid Chemical compound CCC(C(O)=O)C(O)=O UKFXDFUAPNAMPJ-UHFFFAOYSA-N 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- ZIYVHBGGAOATLY-UHFFFAOYSA-L methylmalonate(2-) Chemical compound [O-]C(=O)C(C)C([O-])=O ZIYVHBGGAOATLY-UHFFFAOYSA-L 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000002899 organoaluminium compounds Chemical class 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- DLRJIFUOBPOJNS-UHFFFAOYSA-N phenetole Chemical compound CCOC1=CC=CC=C1 DLRJIFUOBPOJNS-UHFFFAOYSA-N 0.000 description 1
- NCAIGTHBQTXTLR-UHFFFAOYSA-N phentermine hydrochloride Chemical compound [Cl-].CC(C)([NH3+])CC1=CC=CC=C1 NCAIGTHBQTXTLR-UHFFFAOYSA-N 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- 150000008039 phosphoramides Chemical class 0.000 description 1
- 238000000053 physical method Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- OUULRIDHGPHMNQ-UHFFFAOYSA-N stibane Chemical class [SbH3] OUULRIDHGPHMNQ-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- UBZYKBZMAMTNKW-UHFFFAOYSA-J titanium tetrabromide Chemical compound Br[Ti](Br)(Br)Br UBZYKBZMAMTNKW-UHFFFAOYSA-J 0.000 description 1
- TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/02—Carriers therefor
- C08F4/022—Magnesium halide as support anhydrous or hydrated or complexed by means of a Lewis base for Ziegler-type catalysts
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)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT2627571 | 1971-06-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
PL83672B1 true PL83672B1 (en, 2012) | 1975-12-31 |
Family
ID=11219117
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PL1972156223A PL83672B1 (en, 2012) | 1971-06-25 | 1972-06-23 |
Country Status (27)
Country | Link |
---|---|
US (1) | US4336360A (en, 2012) |
JP (4) | JPS5236153B1 (en, 2012) |
AR (1) | AR192799A1 (en, 2012) |
AT (1) | AT327540B (en, 2012) |
AU (1) | AU471393B2 (en, 2012) |
BE (3) | BE785334A (en, 2012) |
BG (1) | BG26815A3 (en, 2012) |
BR (1) | BR7204175D0 (en, 2012) |
CA (3) | CA1002694A (en, 2012) |
CS (1) | CS175433B2 (en, 2012) |
DD (1) | DD98289A5 (en, 2012) |
DE (3) | DE2230672A1 (en, 2012) |
DK (1) | DK141781B (en, 2012) |
ES (1) | ES404230A1 (en, 2012) |
FI (1) | FI54488C (en, 2012) |
FR (3) | FR2143346B1 (en, 2012) |
GB (3) | GB1387888A (en, 2012) |
HU (1) | HU166276B (en, 2012) |
IL (1) | IL39747A (en, 2012) |
NL (4) | NL160285B (en, 2012) |
PL (1) | PL83672B1 (en, 2012) |
RO (1) | RO62447A (en, 2012) |
SE (1) | SE440508B (en, 2012) |
SU (1) | SU403193A3 (en, 2012) |
TR (1) | TR17593A (en, 2012) |
YU (1) | YU39898B (en, 2012) |
ZA (1) | ZA724335B (en, 2012) |
Families Citing this family (131)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
YU35844B (en) * | 1968-11-25 | 1981-08-31 | Montedison Spa | Process for obtaining catalysts for the polymerization of olefines |
US4107413A (en) | 1971-06-25 | 1978-08-15 | Montedison S.P.A. | Process for the stereoregular polymerization of alpha olefins |
IT967867B (it) * | 1972-09-26 | 1974-03-11 | Montedison Spa | Procedimento per la polimerizzazio ne stereospecifica delle alfa ole fine |
GB1492618A (en) * | 1974-02-01 | 1977-11-23 | Mitsui Petrochemical Ind | Process for preparing highly stereoregular polyolefins and catalyst used therefor |
IT1005486B (it) * | 1974-02-15 | 1976-08-20 | Montedison Spa | Gomme termoplastiche e processo per la loro preparazione |
US4157435A (en) | 1974-08-10 | 1979-06-05 | Mitsui Petrochemical Industries, Ltd. | Process for preparing highly stereoregular polyolefins and catalyst used therefor |
US4354010A (en) * | 1975-01-09 | 1982-10-12 | Imperial Chemical Industries Limited | Transition metal compound |
IT1038179B (it) * | 1975-05-16 | 1979-11-20 | Montedison Spa | Procedimento di polimerizzazione di alfa olefine con almeno treatoni di carbonto |
US4234710A (en) | 1976-07-08 | 1980-11-18 | Phillips Petroleum Company | Catalyst and a polymerization process employing the catalyst |
IT1042180B (it) * | 1975-08-29 | 1980-01-30 | Montedison Spa | Polimeri e copolimeri cristallini del propolene e procedimento per la loro preparazione |
IT1054410B (it) * | 1975-11-21 | 1981-11-10 | Mitsui Petrochemical Ind | Catalizzatori per la polimerizzazione delle alfa olefine |
DK151969C (da) * | 1975-11-21 | 1988-07-11 | Montedison Spa | Fast katalysatorkomponent til anvendelse i katalysatorer til brug ved polymerisation af alfa-alkener |
DE2553104A1 (de) * | 1975-11-26 | 1977-06-08 | Mitsui Petrochemical Ind | Verfahren zur herstellung einer auf einen traeger mit hoher leistungsfaehigkeit aufgebrachten katalysatorkomponente |
SE7613662L (sv) | 1975-12-10 | 1977-06-11 | Mitsui Petrochemical Ind | Polymerisation av alfa-olefiner |
IT1054584B (it) * | 1976-01-30 | 1981-11-30 | Montedison Spa | Modificazione cristallina del cloruro di magnesio anidro |
JPS52104593A (en) | 1976-03-01 | 1977-09-02 | Mitsui Petrochem Ind Ltd | Polymerization of olefins |
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- NL NL160286D patent/NL160286C/xx active
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1972
- 1972-06-22 NL NL7208556.A patent/NL160285B/xx not_active Application Discontinuation
- 1972-06-22 NL NL7208558.A patent/NL160286B/xx not_active Application Discontinuation
- 1972-06-22 DK DK311572AA patent/DK141781B/da unknown
- 1972-06-22 SE SE7208279A patent/SE440508B/xx unknown
- 1972-06-22 FI FI1797/72A patent/FI54488C/fi active
- 1972-06-22 BG BG020805A patent/BG26815A3/xx unknown
- 1972-06-22 NL NL7208567.A patent/NL160287B/xx not_active Application Discontinuation
- 1972-06-23 DE DE19722230672 patent/DE2230672A1/de active Granted
- 1972-06-23 DD DD163979A patent/DD98289A5/xx unknown
- 1972-06-23 AR AR242720A patent/AR192799A1/es active
- 1972-06-23 HU HUMO839A patent/HU166276B/hu unknown
- 1972-06-23 IL IL39747A patent/IL39747A/en unknown
- 1972-06-23 CA CA145,602A patent/CA1002694A/en not_active Expired
- 1972-06-23 TR TR17593A patent/TR17593A/xx unknown
- 1972-06-23 BE BE785334A patent/BE785334A/xx not_active IP Right Cessation
- 1972-06-23 ZA ZA724335A patent/ZA724335B/xx unknown
- 1972-06-23 PL PL1972156223A patent/PL83672B1/pl unknown
- 1972-06-23 FR FR7222701A patent/FR2143346B1/fr not_active Expired
- 1972-06-23 CA CA145,603A patent/CA1002695A/en not_active Expired
- 1972-06-23 AU AU43849/72A patent/AU471393B2/en not_active Expired
- 1972-06-23 DE DE19722230728 patent/DE2230728A1/de not_active Withdrawn
- 1972-06-23 FR FR7222703A patent/FR2143348B1/fr not_active Expired
- 1972-06-23 CS CS4455A patent/CS175433B2/cs unknown
- 1972-06-23 BE BE785333A patent/BE785333A/xx not_active IP Right Cessation
- 1972-06-23 DE DE19722230752 patent/DE2230752A1/de active Granted
- 1972-06-23 FR FR7222702A patent/FR2143347B1/fr not_active Expired
- 1972-06-23 BE BE785332A patent/BE785332A/xx not_active IP Right Cessation
- 1972-06-23 CA CA145,601A patent/CA1002693A/en not_active Expired
- 1972-06-23 YU YU1666/72A patent/YU39898B/xx unknown
- 1972-06-23 SU SU1804272A patent/SU403193A3/ru active
- 1972-06-24 ES ES404230A patent/ES404230A1/es not_active Expired
- 1972-06-24 JP JP47063647A patent/JPS5236153B1/ja active Pending
- 1972-06-24 JP JP47063646A patent/JPS5239431B1/ja active Pending
- 1972-06-24 JP JP6364872A patent/JPS5323871B1/ja active Pending
- 1972-06-26 BR BR4175/72A patent/BR7204175D0/pt unknown
- 1972-06-26 GB GB2978472A patent/GB1387888A/en not_active Expired
- 1972-06-26 RO RO7200071405A patent/RO62447A/ro unknown
- 1972-06-26 GB GB2978572A patent/GB1387889A/en not_active Expired
- 1972-06-26 AT AT547572A patent/AT327540B/de not_active IP Right Cessation
- 1972-06-26 GB GB2978672A patent/GB1387890A/en not_active Expired
-
1980
- 1980-02-01 US US06/117,789 patent/US4336360A/en not_active Expired - Lifetime
-
1981
- 1981-07-06 JP JP56105443A patent/JPS57119903A/ja active Granted
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