CS214856B2 - Method of making the resin olefine polymere - Google Patents
Method of making the resin olefine polymere Download PDFInfo
- Publication number
- CS214856B2 CS214856B2 CS787772A CS777278A CS214856B2 CS 214856 B2 CS214856 B2 CS 214856B2 CS 787772 A CS787772 A CS 787772A CS 777278 A CS777278 A CS 777278A CS 214856 B2 CS214856 B2 CS 214856B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- catalyst
- catalyst component
- coolant
- reactor
- olefin
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 12
- 239000011347 resin Substances 0.000 title claims description 3
- 229920005989 resin Polymers 0.000 title claims description 3
- 239000003054 catalyst Substances 0.000 claims abstract description 132
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 50
- 239000010936 titanium Substances 0.000 claims abstract description 50
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 50
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 36
- 150000001336 alkenes Chemical class 0.000 claims abstract description 31
- 229920000642 polymer Polymers 0.000 claims abstract description 29
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims abstract description 24
- 238000012685 gas phase polymerization Methods 0.000 claims abstract description 20
- 239000007788 liquid Substances 0.000 claims abstract description 16
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 15
- 229910052751 metal Inorganic materials 0.000 claims abstract description 11
- 239000002184 metal Substances 0.000 claims abstract description 11
- 239000003638 chemical reducing agent Substances 0.000 claims abstract description 10
- 239000002826 coolant Substances 0.000 claims description 50
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 claims description 42
- -1 titanium-aluminum compound compound Chemical class 0.000 claims description 37
- 238000000034 method Methods 0.000 claims description 30
- 230000008569 process Effects 0.000 claims description 23
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 21
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 21
- 239000001282 iso-butane Substances 0.000 claims description 21
- 229910052782 aluminium Inorganic materials 0.000 claims description 20
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 19
- 239000001257 hydrogen Substances 0.000 claims description 19
- 229910052739 hydrogen Inorganic materials 0.000 claims description 19
- 239000000203 mixture Substances 0.000 claims description 19
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 17
- 239000005977 Ethylene Substances 0.000 claims description 15
- 150000002681 magnesium compounds Chemical class 0.000 claims description 11
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 9
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- 239000001301 oxygen Substances 0.000 claims description 9
- 229910052760 oxygen Inorganic materials 0.000 claims description 9
- 150000001298 alcohols Chemical class 0.000 claims description 7
- 229920000098 polyolefin Polymers 0.000 claims description 7
- 150000001335 aliphatic alkanes Chemical class 0.000 claims description 5
- 239000007795 chemical reaction product Substances 0.000 claims description 4
- 230000009849 deactivation Effects 0.000 claims description 4
- 239000000110 cooling liquid Substances 0.000 claims description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 4
- 229910000041 hydrogen chloride Inorganic materials 0.000 claims 4
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 claims 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 1
- 239000012808 vapor phase Substances 0.000 abstract description 10
- 230000000379 polymerizing effect Effects 0.000 abstract 1
- 238000010791 quenching Methods 0.000 abstract 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 51
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 13
- 238000002156 mixing Methods 0.000 description 13
- 239000000243 solution Substances 0.000 description 11
- 239000007789 gas Substances 0.000 description 10
- 239000000178 monomer Substances 0.000 description 10
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 9
- 239000003085 diluting agent Substances 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 6
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 6
- 239000012071 phase Substances 0.000 description 6
- 229920013716 polyethylene resin Polymers 0.000 description 6
- 229910052723 transition metal Inorganic materials 0.000 description 6
- 150000003623 transition metal compounds Chemical class 0.000 description 6
- 150000003624 transition metals Chemical class 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000007865 diluting Methods 0.000 description 5
- 150000004820 halides Chemical class 0.000 description 5
- 230000002779 inactivation Effects 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 239000012190 activator Substances 0.000 description 4
- 125000005234 alkyl aluminium group Chemical group 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- UAIZDWNSWGTKFZ-UHFFFAOYSA-L ethylaluminum(2+);dichloride Chemical compound CC[Al](Cl)Cl UAIZDWNSWGTKFZ-UHFFFAOYSA-L 0.000 description 4
- 150000002431 hydrogen Chemical class 0.000 description 4
- 229910052749 magnesium Inorganic materials 0.000 description 4
- 239000011777 magnesium Substances 0.000 description 4
- BKIMMITUMNQMOS-UHFFFAOYSA-N nonane Chemical compound CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 150000003608 titanium Chemical class 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
- 125000004414 alkyl thio group Chemical group 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 150000001805 chlorine compounds Chemical class 0.000 description 3
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 150000004678 hydrides Chemical group 0.000 description 3
- 239000003701 inert diluent Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- 239000006228 supernatant Substances 0.000 description 3
- 150000003609 titanium compounds Chemical class 0.000 description 3
- 229910052720 vanadium Inorganic materials 0.000 description 3
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 3
- RVDLHGSZWAELAU-UHFFFAOYSA-N 5-tert-butylthiophene-2-carbonyl chloride Chemical compound CC(C)(C)C1=CC=C(C(Cl)=O)S1 RVDLHGSZWAELAU-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical group CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 150000004703 alkoxides Chemical class 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000001273 butane Substances 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000011949 solid catalyst Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical group CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical group CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- YHWCPXVTRSHPNY-UHFFFAOYSA-N butan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] YHWCPXVTRSHPNY-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UBAZGMLMVVQSCD-UHFFFAOYSA-N carbon dioxide;molecular oxygen Chemical compound O=O.O=C=O UBAZGMLMVVQSCD-UHFFFAOYSA-N 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 229940117975 chromium trioxide Drugs 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N chromium trioxide Inorganic materials O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- GAMDZJFZMJECOS-UHFFFAOYSA-N chromium(6+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Cr+6] GAMDZJFZMJECOS-UHFFFAOYSA-N 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 150000001924 cycloalkanes Chemical class 0.000 description 1
- DIOQZVSQGTUSAI-NJFSPNSNSA-N decane Chemical compound CCCCCCCCC[14CH3] DIOQZVSQGTUSAI-NJFSPNSNSA-N 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical group CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 1
- BICAGYDGRXJYGD-UHFFFAOYSA-N hydrobromide;hydrochloride Chemical compound Cl.Br BICAGYDGRXJYGD-UHFFFAOYSA-N 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000000415 inactivating effect Effects 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- DIOQZVSQGTUSAI-UHFFFAOYSA-N n-butylhexane Natural products CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 230000000153 supplemental effect Effects 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
- 150000003755 zirconium compounds Chemical class 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/18—Stationary reactors having moving elements inside
- B01J19/1868—Stationary reactors having moving elements inside resulting in a loop-type movement
- B01J19/1881—Stationary reactors having moving elements inside resulting in a loop-type movement externally, i.e. the mixture leaving the vessel and subsequently re-entering it
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
- B01J8/08—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with moving particles
- B01J8/10—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with moving particles moved by stirrers or by rotary drums or rotary receptacles or endless belts
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
- B01J8/18—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles
- B01J8/24—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles according to "fluidised-bed" technique
- B01J8/36—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles according to "fluidised-bed" technique with fluidised bed through which there is an essentially horizontal flow of particles
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J8/00—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
- B01J8/18—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles
- B01J8/24—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles according to "fluidised-bed" technique
- B01J8/38—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles according to "fluidised-bed" technique with fluidised bed containing a rotatable device or being subject to rotation or to a circulatory movement, i.e. leaving a vessel and subsequently re-entering it
- B01J8/382—Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with fluidised particles according to "fluidised-bed" technique with fluidised bed containing a rotatable device or being subject to rotation or to a circulatory movement, i.e. leaving a vessel and subsequently re-entering it with a rotatable device only
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J2219/18—Details relating to the spatial orientation of the reactor
- B01J2219/182—Details relating to the spatial orientation of the reactor horizontal
-
- 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
- C08F2410/00—Features related to the catalyst preparation, the catalyst use or to the deactivation of the catalyst
- C08F2410/08—Presence of a deactivator
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/584—Recycling of catalysts
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S526/901—Monomer polymerized in vapor state in presence of transition metal containing catalyst
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Combustion & Propulsion (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Polymerisation Methods In General (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US05/854,831 US4130699A (en) | 1977-11-25 | 1977-11-25 | Vapor phase polymerization with temporarily inactive titanium catalyst |
Publications (1)
Publication Number | Publication Date |
---|---|
CS214856B2 true CS214856B2 (en) | 1982-06-25 |
Family
ID=25319628
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CS787772A CS214856B2 (en) | 1977-11-25 | 1978-11-27 | Method of making the resin olefine polymere |
Country Status (17)
Country | Link |
---|---|
US (1) | US4130699A (de) |
JP (1) | JPS5483084A (de) |
AT (1) | AT367774B (de) |
BE (1) | BE872247A (de) |
BR (1) | BR7807718A (de) |
CA (1) | CA1103396A (de) |
CS (1) | CS214856B2 (de) |
DD (1) | DD140050A5 (de) |
DE (1) | DE2850335A1 (de) |
FR (1) | FR2410007A1 (de) |
GB (1) | GB2008597B (de) |
IN (1) | IN150336B (de) |
IT (1) | IT1107674B (de) |
MX (1) | MX149390A (de) |
NL (1) | NL185012C (de) |
PL (1) | PL114316B1 (de) |
YU (1) | YU272978A (de) |
Families Citing this family (37)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
USRE30148E (en) * | 1974-12-16 | 1979-11-13 | Standard Oil Company (Indiana) | Melt finishing process for polymers produced by vapor state polymerization processes |
DE2966150D1 (en) * | 1978-03-23 | 1983-10-20 | Ici Plc | Gas-phase olefin polymerisation system and process for operating it |
DE2841715A1 (de) * | 1978-09-25 | 1980-04-10 | Basf Ag | Verfahren zum herstellen von homo- und copolymerisaten von alpha -monoolefinen |
US4210559A (en) * | 1978-10-30 | 1980-07-01 | Standard Oil Company (Indiana) | Catalyst for the preparation of polyalpha-olefins having broad molecular weight distributions |
US4233182A (en) * | 1978-12-26 | 1980-11-11 | Standard Oil Company (Indiana) | High activity catalyst for the polymerization of alpha-olefins |
US4313850A (en) * | 1979-10-15 | 1982-02-02 | Standard Oil Company (Indiana) | Catalyst for the polymerization of alpha-olefins |
US4324691A (en) * | 1980-01-10 | 1982-04-13 | Imperial Chemical Industries Limited | Catalyst component |
US4325835A (en) * | 1980-01-10 | 1982-04-20 | Imperial Chemical Industries Limited | Catalyst component |
JPS56159205A (en) * | 1980-05-14 | 1981-12-08 | Nippon Oil Co Ltd | Equipment for olefin gas-phase polymerization |
JPS56129204A (en) * | 1980-03-14 | 1981-10-09 | Nippon Oil Co Ltd | Apparatus for vapor-phase polymerization of olefin |
US4326048A (en) * | 1980-05-27 | 1982-04-20 | Standard Oil Company (Indiana) | Method for emergency shutdown of gas phase polyolefin reactor |
US4311612A (en) * | 1980-08-25 | 1982-01-19 | Standard Oil Company (Indiana) | Olefin polymerization catalyst |
US4287327A (en) * | 1980-09-29 | 1981-09-01 | Standard Oil Company (Indiana) | Process for controlling polymer particle size in vapor phase polymerization |
JPS581708A (ja) * | 1981-06-25 | 1983-01-07 | Mitsubishi Chem Ind Ltd | ポリオレフインの製造法 |
US4402861A (en) * | 1981-05-05 | 1983-09-06 | Chemplex Company | Polymerization catalyst and method |
US4446288A (en) * | 1981-05-05 | 1984-05-01 | Chemplex Company | Polymerization method |
US4384983A (en) * | 1981-05-26 | 1983-05-24 | Standard Oil Company (Indiana) | Catalyst and process for production of polyolefins of improved morphology |
US4376064A (en) * | 1981-05-26 | 1983-03-08 | Standard Oil Co. (Indiana) | Catalyst and process for production of polyolefins of improved morphology |
US4374753A (en) * | 1981-07-29 | 1983-02-22 | Chemplex Company | Polymerization catalyst and method |
US4478988A (en) * | 1981-07-29 | 1984-10-23 | Chemplex Company | Polymerization method |
US4407727A (en) * | 1982-10-08 | 1983-10-04 | Atlantic Richfield Company | Method of supporting a catalyst on polyolefins |
FR2566781B1 (fr) * | 1984-06-28 | 1986-11-14 | Bp Chimie Sa | Procede de polymerisation ou de copolymerisation d'alpha-olefines en lit fluidise, en presence d'un systeme catalytique ziegler-natta |
US4634744A (en) * | 1985-01-09 | 1987-01-06 | Chemplex Company | Method of catalyst deactivation |
FR2588559B1 (fr) * | 1985-10-11 | 1988-03-11 | Bp Chimie Sa | Procede de polymerisation ou de copolymerisation d'alpha-olefines en presence d'un systeme catalytique ziegler-natta ameliore |
US4921919A (en) * | 1985-12-10 | 1990-05-01 | Amoco Corporation | Method and apparatus for minimizing polymer agglomerate or lump formation in a gas-phase polypropylene polymerization reactor |
US4855370A (en) * | 1986-10-01 | 1989-08-08 | Union Carbide Corporation | Method for reducing sheeting during polymerization of alpha-olefins |
IT1227240B (it) * | 1988-09-29 | 1991-03-27 | Enichem Anic Spa | Procedimento per la polimerizzazione dell'etilene e perla copolimerizzazione dell'etilene con alfa-olefine e catalizzatore relativo |
JP2850427B2 (ja) * | 1989-12-25 | 1999-01-27 | 東ソー株式会社 | ポリオレフィンの製造方法 |
JP2952695B2 (ja) * | 1990-09-04 | 1999-09-27 | 東ソー株式会社 | 立体規則性ポリオレフィンの製造方法 |
DE4130353A1 (de) * | 1991-09-12 | 1993-03-18 | Basf Ag | Verfahren zur herstellung von ziegler-natta-katalysatorsystemen |
US5151397A (en) * | 1991-12-16 | 1992-09-29 | Phillips Petroleum Company | Method of producing metal halide catalyst |
EP1112121B1 (de) * | 1998-08-10 | 2002-11-20 | BP Chemicals Limited | Kontinuierliches gasphasenverfahren zur beschichtung von polymerisationskatalysatoren |
NL1010294C2 (nl) * | 1998-10-12 | 2000-04-13 | Dsm Nv | Werkwijze en inrichting voor de bereiding van een olefine-polymeer. |
JP5484290B2 (ja) * | 2009-11-06 | 2014-05-07 | 日本ポリプロ株式会社 | プロピレン重合反応装置及びプロピレン系ブロック共重合体の製造方法 |
WO2012126759A1 (en) | 2011-03-18 | 2012-09-27 | Ineos Manufacturing Belgium Nv | Propylene-ethylene random copolymer |
US9738761B2 (en) | 2013-01-29 | 2017-08-22 | Ineos Europe Ag | Injection moulded polypropylene articles |
WO2023148259A1 (en) | 2022-02-03 | 2023-08-10 | Ineos Europe Ag | Polyolefin blend containing recycled aluminium |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3002963A (en) * | 1957-04-22 | 1961-10-03 | Phillips Petroleum Co | Gas phase polymerization utilizing a free-settling, fluidized catalyst and reactor system therefor |
US3023203A (en) * | 1957-08-16 | 1962-02-27 | Phillips Petroleum Co | Polymerization process |
US3676415A (en) * | 1968-06-27 | 1972-07-11 | Hoechst Ag | Process for polymerizing {60 -olefins |
US3644318A (en) * | 1968-08-21 | 1972-02-22 | Hoechst Ag | Process for the polymerization of olefins |
DE1795268A1 (de) * | 1968-08-30 | 1972-07-27 | Hoechst Ag | Verfahren zur Polymerisation von Olefinen |
DE1805765C3 (de) * | 1968-10-29 | 1980-09-11 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Polymerisation von Propylen |
DE2001183C3 (de) * | 1970-01-13 | 1980-01-31 | Chemische Werke Huels Ag, 4370 Marl | Verfahren zur Unterbrechung und Wiederingangsetzung von Olefinpolymerisationen |
US3965083A (en) * | 1974-12-16 | 1976-06-22 | Standard Oil Company | Process for the vapor phase polymerization of monomers in a horizontal, quench-cooled, stirred-bed reactor using essentially total off-gas recycle and melt finishing |
US3971768A (en) * | 1974-12-16 | 1976-07-27 | Standard Oil Company (Indiana) | Vapor phase reactor off-gas recycle system for use in the vapor state polymerization of monomers |
NO144570C (no) * | 1974-12-16 | 1981-09-23 | Standard Oil Co | Kontinuerlig fremgangsmaate ved dampfasepolymerisering av en fordampbar polymer, samt apparat for utfoerelse av fremgangsmaaten |
US3957448A (en) * | 1974-12-16 | 1976-05-18 | Standard Oil Company | Divided horizontal reactor for the vapor phase polymerization of monomers at different hydrogen levels |
FR2312512A1 (fr) * | 1975-05-27 | 1976-12-24 | Naphtachimie Sa | Procede de polymerisation des olefines en lit fluidise |
GB1566415A (en) * | 1975-11-14 | 1980-04-30 | Standard Oil Co | Olefin polymerisation catalyst components catalysts comprising said components and olefin polymerisation process |
-
1977
- 1977-11-25 US US05/854,831 patent/US4130699A/en not_active Expired - Lifetime
-
1978
- 1978-10-31 CA CA315,289A patent/CA1103396A/en not_active Expired
- 1978-11-02 IN IN788/DEL/78A patent/IN150336B/en unknown
- 1978-11-07 NL NLAANVRAGE7811060,A patent/NL185012C/xx not_active IP Right Cessation
- 1978-11-17 MX MX175673A patent/MX149390A/es unknown
- 1978-11-20 DE DE19782850335 patent/DE2850335A1/de not_active Withdrawn
- 1978-11-22 GB GB7845582A patent/GB2008597B/en not_active Expired
- 1978-11-22 YU YU02729/78A patent/YU272978A/xx unknown
- 1978-11-23 BR BR7807718A patent/BR7807718A/pt unknown
- 1978-11-23 BE BE191913A patent/BE872247A/xx not_active IP Right Cessation
- 1978-11-24 DD DD78209306A patent/DD140050A5/de unknown
- 1978-11-24 JP JP14520278A patent/JPS5483084A/ja active Granted
- 1978-11-24 IT IT52068/78A patent/IT1107674B/it active
- 1978-11-24 FR FR7833335A patent/FR2410007A1/fr active Granted
- 1978-11-25 PL PL1978211226A patent/PL114316B1/pl unknown
- 1978-11-27 CS CS787772A patent/CS214856B2/cs unknown
- 1978-11-27 AT AT0847478A patent/AT367774B/de not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
US4130699A (en) | 1978-12-19 |
PL211226A1 (pl) | 1979-08-27 |
YU272978A (en) | 1982-06-30 |
JPS5483084A (en) | 1979-07-02 |
GB2008597B (en) | 1982-06-30 |
FR2410007B1 (de) | 1981-01-16 |
IT7852068A0 (it) | 1978-11-24 |
BR7807718A (pt) | 1979-07-31 |
IN150336B (de) | 1982-09-11 |
JPS641483B2 (de) | 1989-01-11 |
BE872247A (fr) | 1979-05-23 |
NL185012C (nl) | 1990-01-02 |
AT367774B (de) | 1982-07-26 |
CA1103396A (en) | 1981-06-16 |
NL185012B (nl) | 1989-08-01 |
NL7811060A (nl) | 1979-05-29 |
FR2410007A1 (fr) | 1979-06-22 |
DD140050A5 (de) | 1980-02-06 |
IT1107674B (it) | 1985-11-25 |
MX149390A (es) | 1983-11-01 |
ATA847478A (de) | 1981-12-15 |
GB2008597A (en) | 1979-06-06 |
PL114316B1 (en) | 1981-01-31 |
DE2850335A1 (de) | 1979-05-31 |
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