TW297026B - - Google Patents

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Info

Publication number: TW297026B
Authority: TW; Taiwan
Prior art keywords: olefin; pseudo; weight; item; propylene
Prior art date: 1991-07-31

Application number

TW081106065A

Other languages

English (en)

Chinese (zh)

Original Assignee

Himont Inc

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1991-07-31

Filing date

1992-07-31

Publication date

1997-02-01

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=11360481&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=TW297026(B) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1992-07-31 Application filed by Himont Inc filed Critical Himont Inc

1997-02-01 Application granted granted Critical

1997-02-01 Publication of TW297026B publication Critical patent/TW297026B/zh

Links

239000007789 gas Substances 0.000 claims description 31
239000000203 mixture Substances 0.000 claims description 26
238000000034 method Methods 0.000 claims description 24
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 24
-1 alkyl alkene Chemical class 0.000 claims description 20
150000001335 aliphatic alkanes Chemical class 0.000 claims description 17
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 17
229920000642 polymer Polymers 0.000 claims description 15
150000001336 alkenes Chemical class 0.000 claims description 14
150000001875 compounds Chemical class 0.000 claims description 14
238000006116 polymerization reaction Methods 0.000 claims description 14
125000000217 alkyl group Chemical group 0.000 claims description 13
239000003054 catalyst Substances 0.000 claims description 13
239000007787 solid Substances 0.000 claims description 12
238000006243 chemical reaction Methods 0.000 claims description 11
125000004429 atom Chemical group 0.000 claims description 10
229920001577 copolymer Polymers 0.000 claims description 10
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 9
239000005977 Ethylene Substances 0.000 claims description 8
239000004711 α-olefin Substances 0.000 claims description 8
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 7
229910052782 aluminium Inorganic materials 0.000 claims description 7
150000002148 esters Chemical class 0.000 claims description 7
230000015572 biosynthetic process Effects 0.000 claims description 6
239000008096 xylene Substances 0.000 claims description 5
229920000089 Cyclic olefin copolymer Polymers 0.000 claims description 4
125000003118 aryl group Chemical group 0.000 claims description 4
125000000753 cycloalkyl group Chemical group 0.000 claims description 4
238000002844 melting Methods 0.000 claims description 4
230000008018 melting Effects 0.000 claims description 4
229920000573 polyethylene Polymers 0.000 claims description 4
229920002959 polymer blend Polymers 0.000 claims description 4
239000011949 solid catalyst Substances 0.000 claims description 4
239000000178 monomer Substances 0.000 claims description 3
238000002360 preparation method Methods 0.000 claims description 3
229910052719 titanium Inorganic materials 0.000 claims description 3
239000010936 titanium Substances 0.000 claims description 3
150000001412 amines Chemical class 0.000 claims description 2
125000004432 carbon atom Chemical group C* 0.000 claims description 2
238000011049 filling Methods 0.000 claims description 2
239000012495 reaction gas Substances 0.000 claims description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims 4
PCTMTFRHKVHKIS-BMFZQQSSSA-N (1s,3r,4e,6e,8e,10e,12e,14e,16e,18s,19r,20r,21s,25r,27r,30r,31r,33s,35r,37s,38r)-3-[(2r,3s,4s,5s,6r)-4-amino-3,5-dihydroxy-6-methyloxan-2-yl]oxy-19,25,27,30,31,33,35,37-octahydroxy-18,20,21-trimethyl-23-oxo-22,39-dioxabicyclo[33.3.1]nonatriaconta-4,6,8,10 Chemical compound C1C=C2C[C@@H](OS(O)(=O)=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2.O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/C=C/C=C/C=C/[C@H](C)[C@@H](O)[C@@H](C)[C@H](C)OC(=O)C[C@H](O)C[C@H](O)CC[C@@H](O)[C@H](O)C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 PCTMTFRHKVHKIS-BMFZQQSSSA-N 0.000 claims 1
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims 1
125000003158 alcohol group Chemical group 0.000 claims 1
230000002079 cooperative effect Effects 0.000 claims 1
150000002170 ethers Chemical class 0.000 claims 1
239000004615 ingredient Substances 0.000 claims 1
150000002576 ketones Chemical class 0.000 claims 1
229910000077 silane Inorganic materials 0.000 claims 1
210000003625 skull Anatomy 0.000 claims 1
230000000707 stereoselective effect Effects 0.000 claims 1
239000013589 supplement Substances 0.000 claims 1
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 21
239000002609 medium Substances 0.000 description 18
239000000463 material Substances 0.000 description 17
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 15
229930195733 hydrocarbon Natural products 0.000 description 12
150000002430 hydrocarbons Chemical class 0.000 description 12
239000012071 phase Substances 0.000 description 12
239000002253 acid Substances 0.000 description 11
239000001257 hydrogen Substances 0.000 description 10
229910052739 hydrogen Inorganic materials 0.000 description 10
239000004215 Carbon black (E152) Substances 0.000 description 9
239000007788 liquid Substances 0.000 description 9
239000001294 propane Substances 0.000 description 9
238000004519 manufacturing process Methods 0.000 description 8
230000033228 biological regulation Effects 0.000 description 7
239000002245 particle Substances 0.000 description 7
230000002441 reversible effect Effects 0.000 description 6
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
239000010408 film Substances 0.000 description 5
238000002156 mixing Methods 0.000 description 5
229910052710 silicon Inorganic materials 0.000 description 5
239000010703 silicon Substances 0.000 description 5
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 4
229910052799 carbon Inorganic materials 0.000 description 4
229910052736 halogen Inorganic materials 0.000 description 4
150000003609 titanium compounds Chemical class 0.000 description 4
238000012546 transfer Methods 0.000 description 4
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 3
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 3
238000004090 dissolution Methods 0.000 description 3
150000002367 halogens Chemical class 0.000 description 3
229910052749 magnesium Inorganic materials 0.000 description 3
239000011777 magnesium Substances 0.000 description 3
239000000243 solution Substances 0.000 description 3
239000002023 wood Substances 0.000 description 3
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
239000004698 Polyethylene Substances 0.000 description 2
239000004793 Polystyrene Substances 0.000 description 2
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
208000027418 Wounds and injury Diseases 0.000 description 2
230000006378 damage Effects 0.000 description 2
230000000694 effects Effects 0.000 description 2
230000005611 electricity Effects 0.000 description 2
238000005516 engineering process Methods 0.000 description 2
239000012530 fluid Substances 0.000 description 2
230000004927 fusion Effects 0.000 description 2
208000014674 injury Diseases 0.000 description 2
QWTDNUCVQCZILF-UHFFFAOYSA-N isopentane Chemical compound CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 2
229920000092 linear low density polyethylene Polymers 0.000 description 2
239000004707 linear low-density polyethylene Substances 0.000 description 2
239000000155 melt Substances 0.000 description 2
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
239000003921 oil Substances 0.000 description 2
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
150000004291 polyenes Chemical class 0.000 description 2
229920002223 polystyrene Polymers 0.000 description 2
238000002407 reforming Methods 0.000 description 2
238000000926 separation method Methods 0.000 description 2
241000894007 species Species 0.000 description 2
238000003786 synthesis reaction Methods 0.000 description 2
239000010409 thin film Substances 0.000 description 2
ZSQCNVWYBBKUHS-UHFFFAOYSA-N (2,3-dimethylphenyl)-phenylmethanone Chemical compound CC1=CC=CC(C(=O)C=2C=CC=CC=2)=C1C ZSQCNVWYBBKUHS-UHFFFAOYSA-N 0.000 description 1
BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 description 1
CNDHHGUSRIZDSL-UHFFFAOYSA-N 1-chlorooctane Chemical compound CCCCCCCCCl CNDHHGUSRIZDSL-UHFFFAOYSA-N 0.000 description 1
CYJQCYXRNNCURD-UHFFFAOYSA-N 2,8-dimethyl-1,3,4,4a,5,9b-hexahydropyrido[4,3-b]indole Chemical compound N1C2=CC=C(C)C=C2C2C1CCN(C)C2 CYJQCYXRNNCURD-UHFFFAOYSA-N 0.000 description 1
RDRFGXIWFMNZRW-UHFFFAOYSA-N 2-(2-pyridin-2-ylphenyl)pyridine Chemical compound N1=CC=CC=C1C1=CC=CC=C1C1=CC=CC=N1 RDRFGXIWFMNZRW-UHFFFAOYSA-N 0.000 description 1
GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
241001070941 Castanea Species 0.000 description 1
235000014036 Castanea Nutrition 0.000 description 1
241000282994 Cervidae Species 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-VVKOMZTBSA-N Dideuterium Chemical compound [2H][2H] UFHFLCQGNIYNRP-VVKOMZTBSA-N 0.000 description 1
102100030796 E3 ubiquitin-protein ligase rififylin Human genes 0.000 description 1
101710128004 E3 ubiquitin-protein ligase rififylin Proteins 0.000 description 1
241000196324 Embryophyta Species 0.000 description 1
229910052691 Erbium Inorganic materials 0.000 description 1
OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
206010015548 Euthanasia Diseases 0.000 description 1
241000272168 Laridae Species 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
241000282376 Panthera tigris Species 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
102000016941 Rho Guanine Nucleotide Exchange Factors Human genes 0.000 description 1
108010053823 Rho Guanine Nucleotide Exchange Factors Proteins 0.000 description 1
206010041349 Somnolence Diseases 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
239000005864 Sulphur Substances 0.000 description 1
RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical group O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000005907 alkyl ester group Chemical group 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
CSDREXVUYHZDNP-UHFFFAOYSA-N alumanylidynesilicon Chemical compound [Al].[Si] CSDREXVUYHZDNP-UHFFFAOYSA-N 0.000 description 1
IMNFDUFMRHMDMM-UHFFFAOYSA-N anhydrous n-heptane Natural products CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 1
KEHFKTBHIMJATM-UHFFFAOYSA-N benzene propane-1-sulfonic acid Chemical compound C(CC)S(=O)(=O)O.C1=CC=CC=C1 KEHFKTBHIMJATM-UHFFFAOYSA-N 0.000 description 1
230000008033 biological extinction Effects 0.000 description 1
229910052797 bismuth Inorganic materials 0.000 description 1
JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
238000007664 blowing Methods 0.000 description 1
210000001124 body fluid Anatomy 0.000 description 1
239000010839 body fluid Substances 0.000 description 1
238000009835 boiling Methods 0.000 description 1
210000004556 brain Anatomy 0.000 description 1
BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 1
238000003763 carbonization Methods 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
229910052804 chromium Inorganic materials 0.000 description 1
239000011651 chromium Substances 0.000 description 1
238000013037 co-molding Methods 0.000 description 1
230000008094 contradictory effect Effects 0.000 description 1
238000005336 cracking Methods 0.000 description 1
239000013078 crystal Substances 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
AFABGHUZZDYHJO-UHFFFAOYSA-N dimethyl butane Natural products CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 1
AMTWCFIAVKBGOD-UHFFFAOYSA-N dioxosilane;methoxy-dimethyl-trimethylsilyloxysilane Chemical compound O=[Si]=O.CO[Si](C)(C)O[Si](C)(C)C AMTWCFIAVKBGOD-UHFFFAOYSA-N 0.000 description 1
239000012738 dissolution medium Substances 0.000 description 1
238000009826 distribution Methods 0.000 description 1
210000005069 ears Anatomy 0.000 description 1
230000008451 emotion Effects 0.000 description 1
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000004744 fabric Substances 0.000 description 1
238000005189 flocculation Methods 0.000 description 1
230000016615 flocculation Effects 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
238000010574 gas phase reaction Methods 0.000 description 1
150000002431 hydrogen Chemical class 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
238000002347 injection Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
238000009434 installation Methods 0.000 description 1
230000010354 integration Effects 0.000 description 1
235000015110 jellies Nutrition 0.000 description 1
239000008274 jelly Substances 0.000 description 1
QDLAGTHXVHQKRE-UHFFFAOYSA-N lichenxanthone Natural products COC1=CC(O)=C2C(=O)C3=C(C)C=C(OC)C=C3OC2=C1 QDLAGTHXVHQKRE-UHFFFAOYSA-N 0.000 description 1
239000007791 liquid phase Substances 0.000 description 1
238000004020 luminiscence type Methods 0.000 description 1
238000012423 maintenance Methods 0.000 description 1
230000014759 maintenance of location Effects 0.000 description 1
238000005259 measurement Methods 0.000 description 1
230000001404 mediated effect Effects 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
238000010606 normalization Methods 0.000 description 1
TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
238000012856 packing Methods 0.000 description 1
239000008188 pellet Substances 0.000 description 1
230000002085 persistent effect Effects 0.000 description 1
235000019271 petrolatum Nutrition 0.000 description 1
239000000843 powder Substances 0.000 description 1
238000007639 printing Methods 0.000 description 1
230000000750 progressive effect Effects 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
230000006798 recombination Effects 0.000 description 1
238000005215 recombination Methods 0.000 description 1
238000004064 recycling Methods 0.000 description 1
230000004044 response Effects 0.000 description 1
230000001568 sexual effect Effects 0.000 description 1
150000004756 silanes Chemical class 0.000 description 1
229940083037 simethicone Drugs 0.000 description 1
238000007711 solidification Methods 0.000 description 1
230000008023 solidification Effects 0.000 description 1
230000003595 spectral effect Effects 0.000 description 1
239000004575 stone Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
230000009897 systematic effect Effects 0.000 description 1
239000001648 tannin Substances 0.000 description 1
235000018553 tannin Nutrition 0.000 description 1
229920001864 tannin Polymers 0.000 description 1
238000012360 testing method Methods 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
150000003623 transition metal compounds Chemical class 0.000 description 1
229910052720 vanadium Inorganic materials 0.000 description 1
GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
238000005406 washing Methods 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
238000004804 winding Methods 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
- C08F297/00—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
- C08F297/06—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type
- C08F297/08—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type polymerising mono-olefins
- C08F297/083—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type polymerising mono-olefins the monomers being ethylene or propylene
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Inorganic Chemistry (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Polymerisation Methods In General (AREA)
Graft Or Block Polymers (AREA)

TW081106065A 1991-07-31 1992-07-31 TW297026B (2)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
ITMI912142A IT1250731B (it)	1991-07-31	1991-07-31	Procedimento per la preparazione di polietilene lineare a bassa densita'

Publications (1)

Publication Number	Publication Date
TW297026B true TW297026B (2)	1997-02-01

Family

ID=11360481

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
TW081106065A TW297026B (2)	1991-07-31	1992-07-31

Country Status (24)

Country	Link
US (1)	US5387749A (2)
EP (2)	EP0525767A1 (2)
JP (1)	JP3239184B2 (2)
KR (1)	KR100229255B1 (2)
CN (2)	CN1040986C (2)
AR (1)	AR246749A1 (2)
AT (1)	ATE130015T1 (2)
AU (1)	AU663884B2 (2)
BR (1)	BR9205312A (2)
CA (1)	CA2092921A1 (2)
DE (1)	DE69205960T3 (2)
DK (1)	DK0551485T4 (2)
ES (1)	ES2079881T5 (2)
FI (1)	FI108647B (2)
GR (2)	GR3018043T3 (2)
IL (1)	IL102667A (2)
IT (1)	IT1250731B (2)
MX (1)	MX9204447A (2)
MY (1)	MY108479A (2)
NO (1)	NO300276B1 (2)
RU (1)	RU2120448C1 (2)
TW (1)	TW297026B (2)
WO (1)	WO1993003078A1 (2)
ZA (1)	ZA925664B (2)

Families Citing this family (44)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6025448A (en)	1989-08-31	2000-02-15	The Dow Chemical Company	Gas phase polymerization of olefins
US6538080B1 (en)	1990-07-03	2003-03-25	Bp Chemicals Limited	Gas phase polymerization of olefins
EP0574821B1 (en) *	1992-06-18	1998-03-11	Montell Technology Company bv	Process and apparatus for the gas-phase polymerization of olefins
IT1269194B (it) *	1994-01-21	1997-03-21	Spherilene Srl	Composizioni polimeriche ad elevata processabilita' basate su lldpe
US5455303A (en)	1994-06-20	1995-10-03	Montell North America Inc.	Linear low density polyethylene based compositions with improved optics
US5589539A (en) *	1994-11-23	1996-12-31	Union Carbide Chemicals & Plastics Technology Corporation	Process for preparing an in situ polyethylene blend
KR100269845B1 (ko) *	1994-12-16	2000-10-16	미우라 아끼라	에틸렌 중합체(ethylene polymer)
EP0677624A3 (de) *	1995-06-07	1996-11-13	Sarna Patent & Lizenz Ag	Kunststoffdichtungsbahnen.
IT1276120B1 (it) *	1995-11-14	1997-10-24	Montell Technology Company Bv	Film multistrato estensibili basati su lldpe
IT1276121B1 (it) *	1995-11-14	1997-10-24	Montell Technology Company Bv	Film multistrato estensibili
IT1277095B1 (it) *	1995-12-18	1997-11-04	Montell Technology Company Bv	Film termoretraibili multistrato
IT1281198B1 (it)	1995-12-18	1998-02-17	Montell Technology Company Bv	Film termoretraibili basati su composizioni poliolefiniche comprendenti un copolimero lineare dell'etilene con alfa-olefine
DE19604520A1 (de) *	1996-02-08	1997-08-14	Buna Sow Leuna Olefinverb Gmbh	Polyethylenblend
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1991
- 1991-07-31 IT ITMI912142A patent/IT1250731B/it active IP Right Grant
1992
- 1992-07-27 MY MYPI92001337A patent/MY108479A/en unknown
- 1992-07-28 ZA ZA925664A patent/ZA925664B/xx unknown
- 1992-07-28 IL IL10266792A patent/IL102667A/en not_active IP Right Cessation
- 1992-07-30 BR BR9205312A patent/BR9205312A/pt not_active IP Right Cessation
- 1992-07-30 MX MX9204447A patent/MX9204447A/es not_active IP Right Cessation
- 1992-07-30 DK DK92916690T patent/DK0551485T4/da active
- 1992-07-30 EP EP92113006A patent/EP0525767A1/en active Pending
- 1992-07-30 AU AU23792/92A patent/AU663884B2/en not_active Ceased
- 1992-07-30 AT AT92916690T patent/ATE130015T1/de not_active IP Right Cessation
- 1992-07-30 AR AR92322850A patent/AR246749A1/es active
- 1992-07-30 JP JP50325893A patent/JP3239184B2/ja not_active Expired - Fee Related
- 1992-07-30 WO PCT/EP1992/001731 patent/WO1993003078A1/en not_active Ceased
- 1992-07-30 DE DE69205960T patent/DE69205960T3/de not_active Expired - Lifetime
- 1992-07-30 CA CA002092921A patent/CA2092921A1/en not_active Abandoned
- 1992-07-30 ES ES92916690T patent/ES2079881T5/es not_active Expired - Lifetime
- 1992-07-30 EP EP92916690A patent/EP0551485B2/en not_active Expired - Lifetime
- 1992-07-30 US US08/030,053 patent/US5387749A/en not_active Expired - Lifetime
- 1992-07-30 RU RU93005129/04A patent/RU2120448C1/ru not_active IP Right Cessation
- 1992-07-31 CN CN92110113A patent/CN1040986C/zh not_active Expired - Lifetime
- 1992-07-31 TW TW081106065A patent/TW297026B/zh active
1993
- 1993-01-30 KR KR1019930700273A patent/KR100229255B1/ko not_active Expired - Fee Related
- 1993-03-16 NO NO930940A patent/NO300276B1/no unknown
- 1993-03-29 FI FI931406A patent/FI108647B/fi not_active IP Right Cessation
1995
- 1995-11-09 GR GR950403014T patent/GR3018043T3/el unknown
1996
- 1996-03-25 CN CN96103678A patent/CN1080269C/zh not_active Expired - Lifetime
2000
- 2000-04-21 GR GR20000400976T patent/GR3033294T3/el not_active IP Right Cessation

Also Published As

Publication number	Publication date
DE69205960D1 (de)	1995-12-14
FI108647B (fi)	2002-02-28
NO300276B1 (no)	1997-05-05
US5387749A (en)	1995-02-07
RU2120448C1 (ru)	1998-10-20
JPH06503852A (ja)	1994-04-28
IT1250731B (it)	1995-04-21
EP0551485A1 (en)	1993-07-21
ZA925664B (en)	1993-04-28
BR9205312A (pt)	1994-09-27
DK0551485T3 (da)	1995-12-27
JP3239184B2 (ja)	2001-12-17
DE69205960T2 (de)	1996-04-25
FI931406A0 (fi)	1993-03-29
FI931406L (fi)	1993-03-29
ITMI912142A0 (it)	1991-07-31
AR246749A1 (es)	1994-09-30
WO1993003078A1 (en)	1993-02-18
MY108479A (en)	1996-09-30
EP0551485B1 (en)	1995-11-08
ES2079881T5 (es)	2000-07-16
ATE130015T1 (de)	1995-11-15
KR100229255B1 (en)	1999-11-01
AU2379292A (en)	1993-03-02
AU663884B2 (en)	1995-10-26
CN1040986C (zh)	1998-12-02
NO930940L (no)	1993-03-16
IL102667A (en)	1995-05-26
CA2092921A1 (en)	1993-02-01
CN1134943A (zh)	1996-11-06
GR3033294T3 (en)	2000-09-29
ES2079881T3 (es)	1996-01-16
MX9204447A (es)	1993-05-01
CN1070653A (zh)	1993-04-07
DE69205960T3 (de)	2000-07-27
EP0525767A1 (en)	1993-02-03
ITMI912142A1 (it)	1993-01-31
CN1080269C (zh)	2002-03-06
NO930940D0 (no)	1993-03-16
GR3018043T3 (en)	1996-02-29
EP0551485B2 (en)	2000-04-19
DK0551485T4 (da)	2000-12-04

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