FI66404C - Foerfarande foer framstaellning av etylenpolymerisat med stor taethet med tillhjaelp av en ti-haltig katalysator - Google Patents
Foerfarande foer framstaellning av etylenpolymerisat med stor taethet med tillhjaelp av en ti-haltig katalysator Download PDFInfo
- Publication number
- FI66404C FI66404C FI791244A FI791244A FI66404C FI 66404 C FI66404 C FI 66404C FI 791244 A FI791244 A FI 791244A FI 791244 A FI791244 A FI 791244A FI 66404 C FI66404 C FI 66404C
- Authority
- FI
- Finland
- Prior art keywords
- premix
- compound
- catalyst
- gas
- reactor
- Prior art date
Links
- 239000003054 catalyst Substances 0.000 claims description 92
- 150000001875 compounds Chemical class 0.000 claims description 71
- 229920000642 polymer Polymers 0.000 claims description 57
- 239000002245 particle Substances 0.000 claims description 49
- 238000000034 method Methods 0.000 claims description 46
- 239000010936 titanium Substances 0.000 claims description 39
- 239000012190 activator Substances 0.000 claims description 36
- 230000008569 process Effects 0.000 claims description 35
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 29
- 239000000203 mixture Substances 0.000 claims description 27
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 23
- 239000005977 Ethylene Substances 0.000 claims description 23
- -1 aromatic carboxylic acids Chemical class 0.000 claims description 23
- 239000000463 material Substances 0.000 claims description 22
- 229920006395 saturated elastomer Polymers 0.000 claims description 22
- 238000006243 chemical reaction Methods 0.000 claims description 18
- 239000000155 melt Substances 0.000 claims description 17
- 150000003609 titanium compounds Chemical class 0.000 claims description 16
- 239000004215 Carbon black (E152) Substances 0.000 claims description 14
- 229920001577 copolymer Polymers 0.000 claims description 14
- 229930195733 hydrocarbon Natural products 0.000 claims description 14
- 238000002360 preparation method Methods 0.000 claims description 14
- 239000000377 silicon dioxide Substances 0.000 claims description 14
- 229910052719 titanium Inorganic materials 0.000 claims description 14
- 150000002681 magnesium compounds Chemical class 0.000 claims description 13
- 239000000178 monomer Substances 0.000 claims description 13
- 125000001931 aliphatic group Chemical group 0.000 claims description 12
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 10
- 229920001519 homopolymer Polymers 0.000 claims description 10
- 229910052801 chlorine Inorganic materials 0.000 claims description 8
- 239000011777 magnesium Substances 0.000 claims description 8
- 125000003118 aryl group Chemical group 0.000 claims description 7
- 239000004711 α-olefin Substances 0.000 claims description 6
- 229910052749 magnesium Inorganic materials 0.000 claims description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- 125000005907 alkyl ester group Chemical group 0.000 claims description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 4
- 230000003197 catalytic effect Effects 0.000 claims description 3
- 150000004292 cyclic ethers Chemical class 0.000 claims description 2
- 239000007788 liquid Substances 0.000 claims description 2
- 238000010574 gas phase reaction Methods 0.000 claims 1
- 239000007789 gas Substances 0.000 description 63
- 238000006116 polymerization reaction Methods 0.000 description 25
- 230000000694 effects Effects 0.000 description 20
- 239000000047 product Substances 0.000 description 19
- 230000004913 activation Effects 0.000 description 18
- 229910052782 aluminium Inorganic materials 0.000 description 18
- 238000009826 distribution Methods 0.000 description 16
- 229920000573 polyethylene Polymers 0.000 description 14
- 239000000460 chlorine Substances 0.000 description 13
- 239000010419 fine particle Substances 0.000 description 12
- 239000002904 solvent Substances 0.000 description 12
- 239000000243 solution Substances 0.000 description 11
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 10
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 10
- QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 10
- 238000002156 mixing Methods 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 9
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 8
- 239000002002 slurry Substances 0.000 description 8
- 238000005243 fluidization Methods 0.000 description 7
- 150000002430 hydrocarbons Chemical class 0.000 description 7
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 230000036961 partial effect Effects 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 229910052786 argon Inorganic materials 0.000 description 4
- 239000008187 granular material Substances 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 4
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 4
- 238000012546 transfer Methods 0.000 description 4
- 239000011701 zinc Substances 0.000 description 4
- 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
- SXSVTGQIXJXKJR-UHFFFAOYSA-N [Mg].[Ti] Chemical compound [Mg].[Ti] SXSVTGQIXJXKJR-UHFFFAOYSA-N 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 230000006835 compression Effects 0.000 description 3
- 238000007906 compression Methods 0.000 description 3
- 239000003085 diluting agent Substances 0.000 description 3
- 238000001746 injection moulding Methods 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 239000002685 polymerization catalyst Substances 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 3
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 description 2
- 239000012876 carrier material Substances 0.000 description 2
- UHZZMRAGKVHANO-UHFFFAOYSA-M chlormequat chloride Chemical compound [Cl-].C[N+](C)(C)CCCl UHZZMRAGKVHANO-UHFFFAOYSA-M 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- BPIUIOXAFBGMNB-UHFFFAOYSA-N 1-hexoxyhexane Chemical compound CCCCCCOCCCCCC BPIUIOXAFBGMNB-UHFFFAOYSA-N 0.000 description 1
- ONIKNECPXCLUHT-UHFFFAOYSA-N 2-chlorobenzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1Cl ONIKNECPXCLUHT-UHFFFAOYSA-N 0.000 description 1
- RFONJRMUUALMBA-UHFFFAOYSA-N 2-methanidylpropane Chemical compound CC(C)[CH2-] RFONJRMUUALMBA-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- 101100008638 Caenorhabditis elegans daf-1 gene Proteins 0.000 description 1
- 239000002879 Lewis base Substances 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
- CQBWEBXPMRPCSI-UHFFFAOYSA-M O[Cr](O[SiH3])(=O)=O Chemical compound O[Cr](O[SiH3])(=O)=O CQBWEBXPMRPCSI-UHFFFAOYSA-M 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical class Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 210000003323 beak Anatomy 0.000 description 1
- CPRBYEAAQYKQKD-UHFFFAOYSA-N bis(2,2-diethylbutyl)-ethylalumane Chemical compound C(C)C(C[Al](CC(CC)(CC)CC)CC)(CC)CC CPRBYEAAQYKQKD-UHFFFAOYSA-N 0.000 description 1
- 235000015895 biscuits Nutrition 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 235000014121 butter Nutrition 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000012986 chain transfer agent Substances 0.000 description 1
- 238000003889 chemical engineering Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- GCPCLEKQVMKXJM-UHFFFAOYSA-N ethoxy(diethyl)alumane Chemical group CCO[Al](CC)CC GCPCLEKQVMKXJM-UHFFFAOYSA-N 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 229920006158 high molecular weight polymer Polymers 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 150000007527 lewis bases Chemical class 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000000399 optical microscopy Methods 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000003134 recirculating effect Effects 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000012106 screening analysis Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000010408 sweeping Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229920006029 tetra-polymer Polymers 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- 229910052725 zinc 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
-
- 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
- C08F110/00—Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F110/02—Ethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/16—Copolymers of ethene with alpha-alkenes, e.g. EP rubbers
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)
- Laminated Bodies (AREA)
- Injection Moulding Of Plastics Or The Like (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US96927578A | 1978-12-14 | 1978-12-14 | |
| US96927578 | 1978-12-14 | ||
| US1271279 | 1979-02-16 | ||
| US06/012,712 US4303771A (en) | 1978-12-14 | 1979-02-16 | Process for the preparation of high density ethylene polymers in fluid bed reactor |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI791244A FI791244A (fi) | 1980-06-15 |
| FI66404B FI66404B (fi) | 1984-06-29 |
| FI66404C true FI66404C (fi) | 1984-10-10 |
Family
ID=26683911
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI791244A FI66404C (fi) | 1978-12-14 | 1979-04-17 | Foerfarande foer framstaellning av etylenpolymerisat med stor taethet med tillhjaelp av en ti-haltig katalysator |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US4303771A (no) |
| EP (1) | EP0012147B1 (no) |
| KR (1) | KR830000530B1 (no) |
| AR (1) | AR228565A1 (no) |
| AT (1) | AT364532B (no) |
| AU (1) | AU528281B2 (no) |
| BR (1) | BR7901941A (no) |
| CA (1) | CA1118149A (no) |
| DE (1) | DE2967444D1 (no) |
| DK (1) | DK131679A (no) |
| ES (1) | ES479105A1 (no) |
| FI (1) | FI66404C (no) |
| GR (1) | GR73001B (no) |
| HU (1) | HU181980B (no) |
| MX (1) | MX150171A (no) |
| NO (1) | NO156412C (no) |
| NZ (1) | NZ190054A (no) |
| PT (1) | PT69418A (no) |
Families Citing this family (60)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4379758A (en) * | 1980-12-24 | 1983-04-12 | Union Carbide Corporation | Catalyst composition for polymerizing ethylene |
| DE3243612A1 (de) * | 1982-02-20 | 1983-11-03 | Chemische Werke Hüls AG, 4370 Marl | Verfahren zur herstellung von masshaltigen hohlprofilen aus aliphatischen polyamiden und deren verwendung |
| FR2566782B1 (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 |
| 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 |
| US4670526A (en) * | 1986-02-27 | 1987-06-02 | Union Carbide Corporation | Process for activation of titanium and vanadium catalysts useful in ethylene polymerization |
| US4719193A (en) * | 1986-09-30 | 1988-01-12 | Union Carbide Corporation | Processes for preparing polyethylene catalysts by heating catalyst precursors |
| US5149738A (en) * | 1988-11-16 | 1992-09-22 | Union Carbide Chemicals & Plastics Technology Corporation | Process for the in situ blending of polymers |
| US5047468A (en) * | 1988-11-16 | 1991-09-10 | Union Carbide Chemicals And Plastics Technology Corporation | Process for the in situ blending of polymers |
| US5126398A (en) * | 1988-11-16 | 1992-06-30 | Union Carbide Chemicals & Plastics Technology Corporation | Process for the in situ blending of polymers |
| US5763547A (en) * | 1992-10-02 | 1998-06-09 | The Dow Chemical Company | Supported catalyst complexes for olefin in polymerization |
| US6025448A (en) * | 1989-08-31 | 2000-02-15 | The Dow Chemical Company | Gas phase polymerization of olefins |
| US5106927A (en) * | 1989-09-11 | 1992-04-21 | Union Carbide Chemicals & Plastics Technology Corporation | Process for producing ethylene/propylene/ethylidene norbornene rubbers |
| US6538080B1 (en) | 1990-07-03 | 2003-03-25 | Bp Chemicals Limited | Gas phase polymerization of olefins |
| KR940000014B1 (ko) * | 1990-10-10 | 1994-01-05 | 한국과학기술원 | Hdpe 및 lldpe 중합용 고활성 찌이글러-나타 촉매의 합성 |
| US5102841A (en) * | 1990-12-11 | 1992-04-07 | Union Carbide Chemicals & Plastics Technology Corporation | Process for the production of polyethylene |
| US5525695A (en) | 1991-10-15 | 1996-06-11 | The Dow Chemical Company | Elastic linear interpolymers |
| US5395471A (en) * | 1991-10-15 | 1995-03-07 | The Dow Chemical Company | High drawdown extrusion process with greater resistance to draw resonance |
| US5278272A (en) | 1991-10-15 | 1994-01-11 | The Dow Chemical Company | Elastic substantialy linear olefin polymers |
| US5582923A (en) * | 1991-10-15 | 1996-12-10 | The Dow Chemical Company | Extrusion compositions having high drawdown and substantially reduced neck-in |
| US5674342A (en) * | 1991-10-15 | 1997-10-07 | The Dow Chemical Company | High drawdown extrusion composition and process |
| US5783638A (en) * | 1991-10-15 | 1998-07-21 | The Dow Chemical Company | Elastic substantially linear ethylene polymers |
| US5442018A (en) * | 1994-04-01 | 1995-08-15 | Union Carbide Chemicals & Plastics Technology Corporation | Ethylene polymerization using a titanium and vanadium catalyst system in staged reactors |
| US5773106A (en) * | 1994-10-21 | 1998-06-30 | The Dow Chemical Company | Polyolefin compositions exhibiting heat resistivity, low hexane-extractives and controlled modulus |
| US5981818A (en) * | 1995-03-21 | 1999-11-09 | Stone & Webster Engineering Corp. | Integrated cracking and olefins derivative process utilizing dilute olefins |
| JP3959132B2 (ja) | 1996-03-19 | 2007-08-15 | 住友化学株式会社 | アルミニウム化合物含有固体触媒成分、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 |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| US2839515A (en) * | 1955-10-17 | 1958-06-17 | Union Carbide Corp | Copolymers of ethylene and alpha unsaturated olefins |
| CA849081A (en) * | 1967-03-02 | 1970-08-11 | Du Pont Of Canada Limited | PRODUCTION OF ETHYLENE/.alpha.-OLEFIN COPOLYMERS OF IMPROVED PHYSICAL PROPERTIES |
| CA920299A (en) * | 1968-08-01 | 1973-01-30 | Mitsui Petrochemical Industries | Process for the polymerization and/or copolymerization of olefins with use of ziegler-type catalytsts supported on carrier |
| NL163523C (nl) * | 1970-07-31 | 1983-11-16 | Montedison Spa | Werkwijze om een polymerisatiekatalysator te bereiden. |
| US4107414A (en) * | 1971-06-25 | 1978-08-15 | Montecatini Edison S.P.A. | Process for the stereoregular polymerization of alpha olefins |
| US4107413A (en) * | 1971-06-25 | 1978-08-15 | Montedison S.P.A. | Process for the stereoregular polymerization of alpha olefins |
| JPS5210916B1 (no) * | 1971-07-22 | 1977-03-26 | ||
| GB1415898A (en) * | 1972-02-11 | 1975-12-03 | Huels Chemische Werke Ag | Manufacture of low-density ethylene polymers |
| US4107415A (en) * | 1972-09-26 | 1978-08-15 | Montecatini Edison S.P.A. | Process for the stereospecific polymerization of alpha-olefins |
| NL177314C (nl) * | 1974-04-08 | 1985-09-02 | Mitsubishi Chem Ind | Werkwijze voor het bereiden van een katalysatorcomplex, en werkwijze voor het polymeriseren van een alkeen met deze katalysator. |
| IT1037112B (it) * | 1975-03-28 | 1979-11-10 | Montedison Spa | Catalizzatori per la polimerizzazione delle olfine |
| FR2312512A1 (fr) * | 1975-05-27 | 1976-12-24 | Naphtachimie Sa | Procede de polymerisation des olefines en lit fluidise |
| IT1054410B (it) * | 1975-11-21 | 1981-11-10 | Mitsui Petrochemical Ind | Catalizzatori per la polimerizzazione delle alfa olefine |
| JPS52104593A (en) * | 1976-03-01 | 1977-09-02 | Mitsui Petrochem Ind Ltd | Polymerization of olefins |
-
1979
- 1979-02-16 US US06/012,712 patent/US4303771A/en not_active Expired - Lifetime
- 1979-03-28 CA CA000324360A patent/CA1118149A/en not_active Expired
- 1979-03-30 NO NO791069A patent/NO156412C/no unknown
- 1979-03-30 DK DK131679A patent/DK131679A/da not_active Application Discontinuation
- 1979-03-30 BR BR790941A patent/BR7901941A/pt unknown
- 1979-03-30 AR AR276004A patent/AR228565A1/es active
- 1979-03-30 EP EP79100955A patent/EP0012147B1/en not_active Expired
- 1979-03-30 ES ES479105A patent/ES479105A1/es not_active Expired
- 1979-03-30 AU AU45654/79A patent/AU528281B2/en not_active Ceased
- 1979-03-30 NZ NZ190054A patent/NZ190054A/xx unknown
- 1979-03-30 DE DE7979100955T patent/DE2967444D1/de not_active Expired
- 1979-03-30 AT AT0238479A patent/AT364532B/de not_active IP Right Cessation
- 1979-03-30 PT PT69418A patent/PT69418A/pt unknown
- 1979-03-30 MX MX177144A patent/MX150171A/es unknown
- 1979-03-30 HU HU79UI275A patent/HU181980B/hu not_active IP Right Cessation
- 1979-03-30 GR GR58735A patent/GR73001B/el unknown
- 1979-04-03 KR KR1019790001044A patent/KR830000530B1/ko active
- 1979-04-17 FI FI791244A patent/FI66404C/fi not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| NZ190054A (en) | 1981-04-24 |
| EP0012147B1 (en) | 1985-05-02 |
| NO156412C (no) | 1987-09-16 |
| ES479105A1 (es) | 1979-12-01 |
| KR830000530B1 (ko) | 1983-03-12 |
| FI66404B (fi) | 1984-06-29 |
| HU181980B (en) | 1983-11-28 |
| US4303771A (en) | 1981-12-01 |
| NO156412B (no) | 1987-06-09 |
| EP0012147A1 (en) | 1980-06-25 |
| FI791244A (fi) | 1980-06-15 |
| PT69418A (en) | 1979-04-01 |
| MX150171A (es) | 1984-03-29 |
| CA1118149A (en) | 1982-02-09 |
| ATA238479A (de) | 1981-03-15 |
| GR73001B (no) | 1984-01-24 |
| AU528281B2 (en) | 1983-04-21 |
| NO791069L (no) | 1980-06-17 |
| DE2967444D1 (en) | 1985-06-05 |
| BR7901941A (pt) | 1980-10-07 |
| AT364532B (de) | 1981-10-27 |
| AR228565A1 (es) | 1983-03-30 |
| DK131679A (da) | 1980-06-15 |
| AU4565479A (en) | 1980-06-19 |
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