RU2104289C1 - Частично кристаллическая полиолефиновая композиция и способ ее получения - Google Patents
Частично кристаллическая полиолефиновая композиция и способ ее получения Download PDFInfo
- Publication number
- RU2104289C1 RU2104289C1 RU93004809A RU93004809A RU2104289C1 RU 2104289 C1 RU2104289 C1 RU 2104289C1 RU 93004809 A RU93004809 A RU 93004809A RU 93004809 A RU93004809 A RU 93004809A RU 2104289 C1 RU2104289 C1 RU 2104289C1
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- RU
- Russia
- Prior art keywords
- fraction
- olefin
- alpha
- composition according
- propene
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 55
- 238000000034 method Methods 0.000 title claims description 15
- 238000002360 preparation method Methods 0.000 title description 4
- 239000004711 α-olefin Substances 0.000 claims abstract description 22
- 210000002196 fr. b Anatomy 0.000 claims abstract description 17
- 210000003918 fraction a Anatomy 0.000 claims abstract description 15
- 229920000642 polymer Polymers 0.000 claims abstract description 6
- 229920000089 Cyclic olefin copolymer Polymers 0.000 claims abstract description 5
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims description 25
- 239000003054 catalyst Substances 0.000 claims description 19
- 239000011777 magnesium Substances 0.000 claims description 17
- 229910052749 magnesium Inorganic materials 0.000 claims description 17
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 14
- 238000006116 polymerization reaction Methods 0.000 claims description 11
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 7
- 239000008096 xylene Substances 0.000 claims description 7
- 239000000178 monomer Substances 0.000 claims description 5
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 claims description 4
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 claims description 4
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 claims description 4
- 239000007788 liquid Substances 0.000 claims description 3
- 229920000098 polyolefin Polymers 0.000 claims description 3
- 230000000707 stereoselective effect Effects 0.000 claims description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 claims 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims 1
- 150000001336 alkenes Chemical class 0.000 abstract description 7
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 abstract description 7
- 239000000126 substance Substances 0.000 abstract 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 26
- -1 polypropylene Polymers 0.000 description 16
- 150000001875 compounds Chemical class 0.000 description 14
- 229920001577 copolymer Polymers 0.000 description 12
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 12
- 238000003466 welding Methods 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 9
- 239000007789 gas Substances 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- 239000012071 phase Substances 0.000 description 8
- 239000007787 solid Substances 0.000 description 8
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 7
- 239000000460 chlorine Substances 0.000 description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 5
- 239000005977 Ethylene Substances 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- 229910052782 aluminium Inorganic materials 0.000 description 5
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 239000011949 solid catalyst Substances 0.000 description 5
- 239000010936 titanium Substances 0.000 description 5
- UWNADWZGEHDQAB-UHFFFAOYSA-N 2,5-dimethylhexane Chemical group CC(C)CCC(C)C UWNADWZGEHDQAB-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 4
- 238000002441 X-ray diffraction Methods 0.000 description 4
- IMNFDUFMRHMDMM-UHFFFAOYSA-N anhydrous n-heptane Natural products CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
- MGWAVDBGNNKXQV-UHFFFAOYSA-N diisobutyl phthalate Chemical compound CC(C)COC(=O)C1=CC=CC=C1C(=O)OCC(C)C MGWAVDBGNNKXQV-UHFFFAOYSA-N 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 150000003609 titanium compounds Chemical class 0.000 description 4
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 230000003197 catalytic effect Effects 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- JWCYDYZLEAQGJJ-UHFFFAOYSA-N dicyclopentyl(dimethoxy)silane Chemical compound C1CCCC1[Si](OC)(OC)C1CCCC1 JWCYDYZLEAQGJJ-UHFFFAOYSA-N 0.000 description 3
- 150000002170 ethers Chemical class 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 125000005843 halogen group Chemical group 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 229920001155 polypropylene Polymers 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 229910052719 titanium Inorganic materials 0.000 description 3
- RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidine Chemical compound CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 description 2
- 229910018516 Al—O Inorganic materials 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 229910001629 magnesium chloride Inorganic materials 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 229920005604 random copolymer Polymers 0.000 description 2
- 230000011514 reflex Effects 0.000 description 2
- 150000003377 silicon compounds Chemical class 0.000 description 2
- 229920002545 silicone oil Polymers 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000012798 spherical particle Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- OUPPKRIDJAMCCA-UHFFFAOYSA-N 1-methoxy-2-(methoxymethyl)-2,3-dimethylbutane Chemical compound COCC(C)(C(C)C)COC OUPPKRIDJAMCCA-UHFFFAOYSA-N 0.000 description 1
- LTMRRSWNXVJMBA-UHFFFAOYSA-L 2,2-diethylpropanedioate Chemical compound CCC(CC)(C([O-])=O)C([O-])=O LTMRRSWNXVJMBA-UHFFFAOYSA-L 0.000 description 1
- POWUJINVZSHIGY-UHFFFAOYSA-N 2,6-di(propan-2-yl)piperidine Chemical compound CC(C)C1CCCC(C(C)C)N1 POWUJINVZSHIGY-UHFFFAOYSA-N 0.000 description 1
- 229910018509 Al—N Inorganic materials 0.000 description 1
- ZKTKKORBVZXJTN-UHFFFAOYSA-N C(C(C)C)C(COC)C(OC)CC(C)C Chemical compound C(C(C)C)C(COC)C(OC)CC(C)C ZKTKKORBVZXJTN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- DKMROQRQHGEIOW-UHFFFAOYSA-N Diethyl succinate Chemical compound CCOC(=O)CCC(=O)OCC DKMROQRQHGEIOW-UHFFFAOYSA-N 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical class OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical compound CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- XMYDKOZNENQEHO-UHFFFAOYSA-N [1-methoxy-2-(methoxymethyl)-3-methylbutan-2-yl]cyclopentane Chemical compound COCC(COC)(C(C)C)C1CCCC1 XMYDKOZNENQEHO-UHFFFAOYSA-N 0.000 description 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical group [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 230000000181 anti-adherent effect Effects 0.000 description 1
- 159000000032 aromatic acids Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 150000005840 aryl radicals Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- UXXXZMDJQLPQPH-UHFFFAOYSA-N bis(2-methylpropyl) carbonate Chemical compound CC(C)COC(=O)OCC(C)C UXXXZMDJQLPQPH-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 description 1
- ROORDVPLFPIABK-UHFFFAOYSA-N diphenyl carbonate Chemical compound C=1C=CC=CC=1OC(=O)OC1=CC=CC=C1 ROORDVPLFPIABK-UHFFFAOYSA-N 0.000 description 1
- DWNAQMUDCDVSLT-UHFFFAOYSA-N diphenyl phthalate Chemical compound C=1C=CC=C(C(=O)OC=2C=CC=CC=2)C=1C(=O)OC1=CC=CC=C1 DWNAQMUDCDVSLT-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- YCNSGSUGQPDYTK-UHFFFAOYSA-N ethyl phenyl carbonate Chemical compound CCOC(=O)OC1=CC=CC=C1 YCNSGSUGQPDYTK-UHFFFAOYSA-N 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 150000002391 heterocyclic compounds Chemical class 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 150000002681 magnesium compounds Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000004005 microsphere Substances 0.000 description 1
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
- 125000004437 phosphorous atom Chemical group 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 150000003021 phthalic acid derivatives Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229920006301 statistical copolymer Polymers 0.000 description 1
- 150000003900 succinic acid esters Chemical class 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
- SQBBHCOIQXKPHL-UHFFFAOYSA-N tributylalumane Chemical compound CCCC[Al](CCCC)CCCC SQBBHCOIQXKPHL-UHFFFAOYSA-N 0.000 description 1
- HFFLGKNGCAIQMO-UHFFFAOYSA-N trichloroacetaldehyde Chemical compound ClC(Cl)(Cl)C=O HFFLGKNGCAIQMO-UHFFFAOYSA-N 0.000 description 1
- 229940099259 vaseline Drugs 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/10—Homopolymers or copolymers of propene
- C08L23/14—Copolymers of propene
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/10—Homopolymers or copolymers of propene
- C08L23/14—Copolymers of propene
- C08L23/142—Copolymers of propene at least partially crystalline copolymers of propene with other olefins
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2308/00—Chemical blending or stepwise polymerisation process with the same catalyst
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Inorganic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Medicinal Preparation (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ITMI920545A IT1254244B (it) | 1992-03-10 | 1992-03-10 | Composizioni di copolimeri random del propene contenenti una alfa- olefina come comonomero |
| ITM192A000545 | 1992-03-10 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU93004809A RU93004809A (ru) | 1996-06-27 |
| RU2104289C1 true RU2104289C1 (ru) | 1998-02-10 |
Family
ID=11362346
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU93004809A RU2104289C1 (ru) | 1992-03-10 | 1993-03-09 | Частично кристаллическая полиолефиновая композиция и способ ее получения |
Country Status (16)
| Country | Link |
|---|---|
| EP (1) | EP0560326B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP3452601B2 (cg-RX-API-DMAC7.html) |
| KR (1) | KR100253015B1 (cg-RX-API-DMAC7.html) |
| CN (1) | CN1082979C (cg-RX-API-DMAC7.html) |
| AT (1) | ATE153683T1 (cg-RX-API-DMAC7.html) |
| AU (1) | AU664598B2 (cg-RX-API-DMAC7.html) |
| BR (1) | BR9301113A (cg-RX-API-DMAC7.html) |
| CA (1) | CA2091299C (cg-RX-API-DMAC7.html) |
| DE (1) | DE69310961T2 (cg-RX-API-DMAC7.html) |
| ES (1) | ES2103990T3 (cg-RX-API-DMAC7.html) |
| FI (1) | FI112245B (cg-RX-API-DMAC7.html) |
| IT (1) | IT1254244B (cg-RX-API-DMAC7.html) |
| MX (1) | MX9301317A (cg-RX-API-DMAC7.html) |
| NO (1) | NO301771B1 (cg-RX-API-DMAC7.html) |
| RU (1) | RU2104289C1 (cg-RX-API-DMAC7.html) |
| TW (1) | TW281681B (cg-RX-API-DMAC7.html) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2275306C2 (ru) * | 2000-06-23 | 2006-04-27 | Випак Вальсроде Гмбх Унд Ко.Кг | Вытянутая многослойная полиолефиновая пленка |
| RU2334766C2 (ru) * | 2001-06-27 | 2008-09-27 | Бореалис Текнолоджи Ой | Полимерная пленка, содержащая статистический сополимер пропилена |
| RU2676711C1 (ru) * | 2015-03-02 | 2019-01-10 | Бореалис Аг | Композиция неупорядоченного c2c3 сополимера с улучшенным балансом между температурой начала сваривания и температурой плавления |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1269307B (it) * | 1994-03-09 | 1997-03-26 | Himont Inc | Film o lastre di polimeri olefinici |
| DE69503560T2 (de) * | 1994-04-28 | 1999-03-18 | Sumitomo Chemical Co., Ltd., Osaka | Polypropylen-Zusammensetzung für laminatete und orientierte Filme sowie daraus bestehender laminateter und orientierter Film |
| CA2164461C (en) * | 1994-12-06 | 2000-08-08 | Tatsuya Tanizaki | Polypropylene composition and uses thereof |
| SG38896A1 (en) * | 1994-12-22 | 1997-04-17 | Sumitomo Chemical Co | Polypropylene composition and laminated and oriented film therefrom |
| US6106938A (en) * | 1994-12-22 | 2000-08-22 | Sumitomo Chemical Company, Ltd. | Polypropylene composition and laminated and oriented film therefrom |
| CN1076282C (zh) * | 1995-03-02 | 2001-12-19 | 三井化学株式会社 | 聚丙烯复合膜 |
| CN1110514C (zh) | 1996-05-06 | 2003-06-04 | 蒙特尔技术有限公司 | 可控剥离强度可热封膜的聚烯烃组合物 |
| EP1025162B1 (en) | 1998-08-20 | 2003-09-03 | Basell Poliolefine Italia S.p.A. | Crystalline propylene copolymer compositions having improved sealability and optical properties and reduced solubility |
| CN1187405C (zh) | 1999-12-16 | 2005-02-02 | 巴塞尔特克美国有限公司 | 包含α－烯烃作为共聚单体的丙烯的无规共聚物的组合物 |
| JP4655344B2 (ja) * | 2000-08-30 | 2011-03-23 | 住友化学株式会社 | プロピレン系共重合体とその製造方法およびそのプロピレン系共重合体からなるフィルム |
| MY132768A (en) | 2001-10-09 | 2007-10-31 | Basell Poliolefine Italia Spa | Crystalline propylene copolymer compositions having improved sealability and optical properties and reduced solubility. |
| EP1827825A1 (en) | 2004-12-21 | 2007-09-05 | Basell Poliolefine Italia S.r.l. | Heat-sealable polyolefin films |
| JP2006350725A (ja) * | 2005-06-16 | 2006-12-28 | Alps Electric Co Ltd | カード装着装置 |
| WO2009077481A1 (en) * | 2007-12-18 | 2009-06-25 | Basell Poliolefine Italia S.R.L. | Membranes |
| WO2011036077A1 (en) | 2009-09-24 | 2011-03-31 | Basell Poliolefine Italia S.R.L. | Heat-sealable polyolefin films |
| WO2011039314A1 (en) | 2009-09-29 | 2011-04-07 | Basell Poliolefine Italia Srl | Heat-sealable polyolefin films |
| US8735498B2 (en) | 2009-11-17 | 2014-05-27 | Basell Poliolefine Italia S.R.L. | Soft polyolefin compositions with improved processability |
| JP5695076B2 (ja) | 2009-11-24 | 2015-04-01 | バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ | 改良したシール性を示すポリオレフィン組成物 |
| JP5701376B2 (ja) * | 2010-04-21 | 2015-04-15 | ボリアリス エージー | シール温度の低いプロピレン／１−ヘキセン共重合体組成物 |
| ATE552303T1 (de) * | 2010-04-21 | 2012-04-15 | Borealis Ag | Propylen-/1-hexen copolymerzusammensetzung mit breitem verarbeitungsfenster für abdichtungen |
| US20130165591A1 (en) | 2010-09-06 | 2013-06-27 | Basell Poliolefine Italia S.R.L. | Polyolefin compositions having improved sealability |
| EP2487203B2 (en) | 2011-02-14 | 2020-11-25 | Borealis AG | Sealing propylene copolymer |
| EP2540499B1 (en) * | 2011-06-27 | 2014-02-26 | Borealis AG | Multi-layer biaxially oriented polymer film |
| EP2540496B1 (en) * | 2011-06-27 | 2014-04-23 | Borealis AG | Multi-layer blown film |
| EP2540497B1 (en) | 2011-06-27 | 2014-08-06 | Borealis AG | Multi-layer cast film |
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| US4481336A (en) * | 1982-03-23 | 1984-11-06 | Mitsubishi Petrochemical Company Limited | Olefinic block copolymers of ethylene propylene and 1-butene |
| US4822840A (en) * | 1986-10-09 | 1989-04-18 | Mitsui Petrochemical Industries, Ltd. | Low-crystalline propylene random copolymer composition, process for production thereof, and polypropylene composite laminated structure |
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| GB1495776A (en) * | 1975-06-11 | 1977-12-21 | Ici Ltd | Film-forming olefin polymer compositions |
| US4211852A (en) * | 1977-09-26 | 1980-07-08 | Mitsui Petrochemical Industries Ltd. | Thermoplastic olefin resin composition and laminated film or sheet thereof |
| JPS56139520A (en) * | 1980-04-02 | 1981-10-31 | Mitsui Petrochem Ind Ltd | Preparation of block copolymer |
| DE4004087A1 (de) * | 1990-02-10 | 1991-08-14 | Basf Ag | Copolymerisate des propylens |
-
1992
- 1992-03-10 IT ITMI920545A patent/IT1254244B/it active
-
1993
- 1993-03-09 NO NO930863A patent/NO301771B1/no not_active IP Right Cessation
- 1993-03-09 CA CA002091299A patent/CA2091299C/en not_active Expired - Fee Related
- 1993-03-09 RU RU93004809A patent/RU2104289C1/ru active
- 1993-03-09 FI FI931040A patent/FI112245B/fi not_active IP Right Cessation
- 1993-03-09 BR BR9301113A patent/BR9301113A/pt not_active IP Right Cessation
- 1993-03-10 DE DE69310961T patent/DE69310961T2/de not_active Expired - Lifetime
- 1993-03-10 MX MX9301317A patent/MX9301317A/es unknown
- 1993-03-10 EP EP93103846A patent/EP0560326B1/en not_active Expired - Lifetime
- 1993-03-10 ES ES93103846T patent/ES2103990T3/es not_active Expired - Lifetime
- 1993-03-10 CN CN93104322A patent/CN1082979C/zh not_active Expired - Fee Related
- 1993-03-10 JP JP07611393A patent/JP3452601B2/ja not_active Expired - Fee Related
- 1993-03-10 AT AT93103846T patent/ATE153683T1/de not_active IP Right Cessation
- 1993-03-10 KR KR1019930003573A patent/KR100253015B1/ko not_active Expired - Fee Related
- 1993-03-10 AU AU35138/93A patent/AU664598B2/en not_active Ceased
- 1993-05-14 TW TW082101774A patent/TW281681B/zh active
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4481336A (en) * | 1982-03-23 | 1984-11-06 | Mitsubishi Petrochemical Company Limited | Olefinic block copolymers of ethylene propylene and 1-butene |
| US4822840A (en) * | 1986-10-09 | 1989-04-18 | Mitsui Petrochemical Industries, Ltd. | Low-crystalline propylene random copolymer composition, process for production thereof, and polypropylene composite laminated structure |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2275306C2 (ru) * | 2000-06-23 | 2006-04-27 | Випак Вальсроде Гмбх Унд Ко.Кг | Вытянутая многослойная полиолефиновая пленка |
| RU2334766C2 (ru) * | 2001-06-27 | 2008-09-27 | Бореалис Текнолоджи Ой | Полимерная пленка, содержащая статистический сополимер пропилена |
| US7683141B2 (en) | 2001-06-27 | 2010-03-23 | Borealis Technology Oy | Polymer film comprising a propylene random copolymer |
| RU2676711C1 (ru) * | 2015-03-02 | 2019-01-10 | Бореалис Аг | Композиция неупорядоченного c2c3 сополимера с улучшенным балансом между температурой начала сваривания и температурой плавления |
Also Published As
| Publication number | Publication date |
|---|---|
| NO930863D0 (no) | 1993-03-09 |
| EP0560326B1 (en) | 1997-05-28 |
| FI931040A0 (fi) | 1993-03-09 |
| AU3513893A (en) | 1993-09-16 |
| CA2091299C (en) | 2001-06-12 |
| ES2103990T3 (es) | 1997-10-01 |
| AU664598B2 (en) | 1995-11-23 |
| NO930863L (no) | 1993-09-13 |
| JPH0693146A (ja) | 1994-04-05 |
| FI112245B (fi) | 2003-11-14 |
| CA2091299A1 (en) | 1993-09-11 |
| DE69310961T2 (de) | 1997-11-27 |
| NO301771B1 (no) | 1997-12-08 |
| CN1082979C (zh) | 2002-04-17 |
| FI931040L (fi) | 1993-09-11 |
| EP0560326A1 (en) | 1993-09-15 |
| ITMI920545A0 (it) | 1992-03-10 |
| IT1254244B (it) | 1995-09-14 |
| ITMI920545A1 (it) | 1993-09-10 |
| MX9301317A (es) | 1993-09-01 |
| BR9301113A (pt) | 1993-09-14 |
| JP3452601B2 (ja) | 2003-09-29 |
| CN1076937A (zh) | 1993-10-06 |
| KR100253015B1 (ko) | 2000-04-15 |
| TW281681B (cg-RX-API-DMAC7.html) | 1996-07-21 |
| DE69310961D1 (de) | 1997-07-03 |
| KR930019750A (ko) | 1993-10-18 |
| ATE153683T1 (de) | 1997-06-15 |
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