NO308172B1 - Materiale av propylen-kopolymerer og fremgangsmÕte for fremstilling av dette - Google Patents

Materiale av propylen-kopolymerer og fremgangsmÕte for fremstilling av dette Download PDF

Info

Publication number: NO308172B1
Authority: NO; Norway
Prior art keywords: weight; olefin; copolymer; propylene; present
Prior art date: 1990-09-28

Application number

NO913788A

Other languages

English (en)

Norwegian (no)

Other versions

NO913788D0 (no

NO913788L (no

Inventor

Massimo Covezzi

Antonio Ciarrocchi

Original Assignee

Montell North America 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.)

1990-09-28

Filing date

1991-09-26

Publication date

2000-08-07

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=11184181&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=NO308172(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1991-09-26 Application filed by Montell North America Inc filed Critical Montell North America Inc

1991-09-26 Publication of NO913788D0 publication Critical patent/NO913788D0/no

1992-03-30 Publication of NO913788L publication Critical patent/NO913788L/no

2000-08-07 Publication of NO308172B1 publication Critical patent/NO308172B1/no

Links

229920001577 copolymer Polymers 0.000 title claims abstract description 16
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 title claims abstract description 10
239000000463 material Substances 0.000 title claims description 26
238000000034 method Methods 0.000 title claims description 14
238000002360 preparation method Methods 0.000 title description 5
239000004711 α-olefin Substances 0.000 claims abstract description 13
229920001155 polypropylene Polymers 0.000 claims abstract description 11
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 10
239000005977 Ethylene Substances 0.000 claims abstract description 10
229920005606 polypropylene copolymer Polymers 0.000 claims abstract description 7
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims abstract description 7
-1 polypropylene Polymers 0.000 claims description 31
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 25
239000003054 catalyst Substances 0.000 claims description 23
238000006116 polymerization reaction Methods 0.000 claims description 15
239000011777 magnesium Substances 0.000 claims description 14
229910052749 magnesium Inorganic materials 0.000 claims description 14
229920000642 polymer Polymers 0.000 claims description 14
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims description 10
238000004519 manufacturing process Methods 0.000 claims description 10
239000004743 Polypropylene Substances 0.000 claims description 9
239000000178 monomer Substances 0.000 claims description 8
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 6
239000008096 xylene Substances 0.000 claims description 6
LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 claims description 4
KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-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
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 4
239000012798 spherical particle Substances 0.000 claims description 3
230000000707 stereoselective effect Effects 0.000 claims description 3
TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims description 2
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 2
239000000203 mixture Substances 0.000 abstract description 6
150000001875 compounds Chemical class 0.000 description 16
239000011888 foil Substances 0.000 description 9
239000012071 phase Substances 0.000 description 9
238000007789 sealing Methods 0.000 description 9
239000011949 solid catalyst Substances 0.000 description 8
XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 8
TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 7
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 7
229910003074 TiCl4 Inorganic materials 0.000 description 7
239000007787 solid Substances 0.000 description 7
239000007789 gas Substances 0.000 description 6
239000007788 liquid Substances 0.000 description 6
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
238000002844 melting Methods 0.000 description 5
230000008018 melting Effects 0.000 description 5
239000002245 particle 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
239000004215 Carbon black (E152) Substances 0.000 description 4
229930195733 hydrocarbon Natural products 0.000 description 4
150000002430 hydrocarbons Chemical class 0.000 description 4
239000000047 product Substances 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
238000002083 X-ray spectrum Methods 0.000 description 3
150000001336 alkenes Chemical class 0.000 description 3
125000000217 alkyl group Chemical group 0.000 description 3
229910052782 aluminium Inorganic materials 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
239000000470 constituent Substances 0.000 description 3
125000005843 halogen group Chemical group 0.000 description 3
229910001629 magnesium chloride Inorganic materials 0.000 description 3
229910052757 nitrogen Inorganic materials 0.000 description 3
238000001228 spectrum Methods 0.000 description 3
238000003756 stirring Methods 0.000 description 3
239000010936 titanium Substances 0.000 description 3
238000011282 treatment Methods 0.000 description 3
238000005406 washing Methods 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
IRIAEXORFWYRCZ-UHFFFAOYSA-N Butylbenzyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 IRIAEXORFWYRCZ-UHFFFAOYSA-N 0.000 description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
238000004566 IR spectroscopy Methods 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
239000012298 atmosphere Substances 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
239000000460 chlorine Substances 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
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 2
238000009826 distribution Methods 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
150000002170 ethers Chemical class 0.000 description 2
238000001914 filtration Methods 0.000 description 2
238000005469 granulation Methods 0.000 description 2
230000003179 granulation Effects 0.000 description 2
150000004820 halides Chemical class 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
229910052739 hydrogen Inorganic materials 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical class ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 2
239000011261 inert gas Substances 0.000 description 2
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
125000004433 nitrogen atom Chemical group N* 0.000 description 2
239000012188 paraffin wax Substances 0.000 description 2
YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
239000002861 polymer material Substances 0.000 description 2
239000012265 solid product Substances 0.000 description 2
239000002904 solvent Substances 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
PVWCLOAAEFMTLH-UHFFFAOYSA-N 4,4-bis(methoxymethyl)-2,6-dimethylheptane Chemical compound COCC(COC)(CC(C)C)CC(C)C PVWCLOAAEFMTLH-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
DKMROQRQHGEIOW-UHFFFAOYSA-N Diethyl succinate Chemical compound CCOC(=O)CCC(=O)OCC DKMROQRQHGEIOW-UHFFFAOYSA-N 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical class OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-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
239000012190 activator Substances 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
159000000032 aromatic acids Chemical class 0.000 description 1
150000005840 aryl radicals Chemical group 0.000 description 1
125000004429 atom Chemical group 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
230000015556 catabolic process Effects 0.000 description 1
238000012512 characterization method Methods 0.000 description 1
150000001805 chlorine compounds Chemical class 0.000 description 1
239000003426 co-catalyst Substances 0.000 description 1
239000002131 composite material Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
239000012967 coordination catalyst Substances 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
150000001991 dicarboxylic acids Chemical class 0.000 description 1
ZVMRWPHIZSSUKP-UHFFFAOYSA-N dicyclohexyl(dimethoxy)silane Chemical compound C1CCCCC1[Si](OC)(OC)C1CCCCC1 ZVMRWPHIZSSUKP-UHFFFAOYSA-N 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
239000002270 dispersing agent Substances 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
238000001035 drying Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
150000002148 esters Chemical class 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
238000002474 experimental method Methods 0.000 description 1
238000000605 extraction Methods 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
239000011521 glass Substances 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
239000007970 homogeneous dispersion Substances 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
150000002596 lactones Chemical class 0.000 description 1
239000007791 liquid phase Substances 0.000 description 1
150000002680 magnesium Chemical class 0.000 description 1
150000002681 magnesium compounds Chemical class 0.000 description 1
239000000155 melt Substances 0.000 description 1
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
150000002763 monocarboxylic acids Chemical class 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
238000004806 packaging method and process Methods 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 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
230000000379 polymerizing effect Effects 0.000 description 1
229920000098 polyolefin Polymers 0.000 description 1
229920001296 polysiloxane Chemical class 0.000 description 1
238000002203 pretreatment Methods 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
238000004062 sedimentation Methods 0.000 description 1
229910000077 silane Inorganic materials 0.000 description 1
150000003377 silicon compounds Chemical class 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
239000007858 starting material Substances 0.000 description 1
150000003900 succinic acid esters Chemical class 0.000 description 1
125000004434 sulfur atom Chemical group 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

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
- C08L23/10—Homopolymers or copolymers of propene
- 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

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)
Crystallography & Structural Chemistry (AREA)
Compositions Of Macromolecular Compounds (AREA)
Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Processes Of Treating Macromolecular Substances (AREA)
Sealing Material Composition (AREA)
Pyrane Compounds (AREA)
Liquid Crystal Substances (AREA)
Adhesives Or Adhesive Processes (AREA)
Graft Or Block Polymers (AREA)

NO913788A 1990-09-28 1991-09-26 Materiale av propylen-kopolymerer og fremgangsmÕte for fremstilling av dette NO308172B1 (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
IT02160190A IT1243430B (it)	1990-09-28	1990-09-28	Composizioni di polimeri cristallini del propilene aventi bassa temperatura

Publications (3)

Publication Number	Publication Date
NO913788D0 NO913788D0 (no)	1991-09-26
NO913788L NO913788L (no)	1992-03-30
NO308172B1 true NO308172B1 (no)	2000-08-07

Family

ID=11184181

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO913788A NO308172B1 (no)	1990-09-28	1991-09-26	Materiale av propylen-kopolymerer og fremgangsmÕte for fremstilling av dette

Country Status (24)

Country	Link
US (1)	US5296548A (fi)
EP (1)	EP0483523B1 (fi)
JP (1)	JP3188492B2 (fi)
KR (1)	KR100199685B1 (fi)
CN (1)	CN1043238C (fi)
AT (1)	ATE147090T1 (fi)
AU (1)	AU650285B2 (fi)
BR (1)	BR9104160A (fi)
CA (1)	CA2052347C (fi)
CZ (1)	CZ283235B6 (fi)
DE (1)	DE69123935T2 (fi)
DK (1)	DK0483523T3 (fi)
FI (1)	FI108646B (fi)
HU (1)	HU211023B (fi)
ID (1)	ID960B (fi)
IT (1)	IT1243430B (fi)
MX (1)	MX9101279A (fi)
MY (1)	MY107790A (fi)
NO (1)	NO308172B1 (fi)
PT (1)	PT99082B (fi)
RU (1)	RU2059670C1 (fi)
SK (1)	SK280077B6 (fi)
TW (1)	TW212191B (fi)
ZA (1)	ZA917576B (fi)

Families Citing this family (42)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
TW221700B (fi) *	1990-11-01	1994-03-11	Himont Inc
IT1254468B (it) *	1992-02-18	1995-09-25	Himont Inc	Composizioni poliolefiniche termosaldabili
CA2098664A1 (en) †	1992-06-30	1993-12-31	Hajime Sadatoshi	Polypropylene random copolymer and film thereof
IT1256235B (it) *	1992-12-23	1995-11-29	Himont Inc	Processo per rivestire la superficie interna di contenitori metallici con materiali poliolefinici
ATE181347T1 (de) *	1993-07-14	1999-07-15	Union Carbide Chem Plastic	Polymerzusammensetzungen
US5338790A (en) *	1993-07-14	1994-08-16	Shell Oil Company	Polymer compositions
IT1269914B (it) *	1994-03-24	1997-04-16	Himonty Inc	Composizioni verniciabili di copolimeri cristallini del propilene aventi bassa temperatura di saldabilita'
AU693917B2 (en) *	1994-09-08	1998-07-09	Showa Denko Kabushiki Kaisha	Propylene block copolymer, process for producing the same and resin composition comprising the same
EP0677624A3 (de) *	1995-06-07	1996-11-13	Sarna Patent & Lizenz Ag	Kunststoffdichtungsbahnen.
DE19543292A1 (de) *	1995-11-21	1997-05-22	Basf Ag	Copolymerisate des Propylens mit anderen C¶2¶-C¶1¶¶0¶-Alk-1-enen
BE1009963A3 (fr) *	1995-12-22	1997-11-04	Solvay	Compositions a base de copolymeres statistiques du propylene, procede pour leur fabrication, et feuilles multicouches thermoscellables les contenant.
WO1997042258A1 (en) *	1996-05-06	1997-11-13	Montell Technology Company B.V.	Polyolefin compositions for heat-sealable films having controlled peel strength
US6060533A (en) *	1998-01-09	2000-05-09	Montell North America Inc.	Process for making foam articles having good low temperature toughness from high melt strength propyline polymer materials
US6436531B1 (en)	1998-07-20	2002-08-20	3M Innovative Properties Company	Polymer blends and tapes therefrom
US6395831B1 (en)	1998-08-20	2002-05-28	Baselltech Usa Inc.	Crystalline propylene copolymer compositions having improved sealability and optical properties and reduced solubility
JP4503115B2 (ja) *	1999-06-09	2010-07-14	株式会社プライムポリマー	プロピレン系ランダム共重合体組成物及びそれからなるフィルム
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1990
- 1990-09-28 IT IT02160190A patent/IT1243430B/it active IP Right Grant
1991
- 1991-09-23 ZA ZA917576A patent/ZA917576B/xx unknown
- 1991-09-23 US US07/763,695 patent/US5296548A/en not_active Expired - Lifetime
- 1991-09-25 TW TW080107540A patent/TW212191B/zh active
- 1991-09-26 FI FI914524A patent/FI108646B/fi active
- 1991-09-26 MX MX9101279A patent/MX9101279A/es unknown
- 1991-09-26 MY MYPI91001738A patent/MY107790A/en unknown
- 1991-09-26 PT PT99082A patent/PT99082B/pt not_active IP Right Cessation
- 1991-09-26 AU AU84813/91A patent/AU650285B2/en not_active Ceased
- 1991-09-26 NO NO913788A patent/NO308172B1/no not_active IP Right Cessation
- 1991-09-27 RU SU915001694A patent/RU2059670C1/ru not_active IP Right Cessation
- 1991-09-27 EP EP91116545A patent/EP0483523B1/en not_active Expired - Lifetime
- 1991-09-27 DE DE69123935T patent/DE69123935T2/de not_active Expired - Lifetime
- 1991-09-27 DK DK91116545.4T patent/DK0483523T3/da active
- 1991-09-27 BR BR9104160-0A patent/BR9104160A/pt not_active IP Right Cessation
- 1991-09-27 SK SK2970-91A patent/SK280077B6/sk unknown
- 1991-09-27 CA CA002052347A patent/CA2052347C/en not_active Expired - Fee Related
- 1991-09-27 AT AT91116545T patent/ATE147090T1/de not_active IP Right Cessation
- 1991-09-27 CZ CS912970A patent/CZ283235B6/cs not_active IP Right Cessation
- 1991-09-27 HU HU913109A patent/HU211023B/hu not_active IP Right Cessation
- 1991-09-28 CN CN91110645A patent/CN1043238C/zh not_active Expired - Lifetime
- 1991-09-28 KR KR1019910016980A patent/KR100199685B1/ko not_active IP Right Cessation
- 1991-09-30 JP JP27822891A patent/JP3188492B2/ja not_active Expired - Fee Related
- 1991-10-29 ID IDP71691A patent/ID960B/id unknown

Also Published As

Publication number	Publication date
MX9101279A (es)	1992-05-04
US5296548A (en)	1994-03-22
DE69123935D1 (de)	1997-02-13
MY107790A (en)	1996-06-15
SK280077B6 (sk)	1999-07-12
EP0483523B1 (en)	1997-01-02
CN1043238C (zh)	1999-05-05
IT9021601A0 (it)	1990-09-28
FI914524A (fi)	1992-03-29
BR9104160A (pt)	1992-06-02
PT99082B (pt)	1999-02-26
CN1061031A (zh)	1992-05-13
NO913788D0 (no)	1991-09-26
KR920006429A (ko)	1992-04-27
RU2059670C1 (ru)	1996-05-10
IT9021601A1 (it)	1992-03-28
AU8481391A (en)	1992-04-02
ZA917576B (en)	1992-06-24
CZ283235B6 (cs)	1998-02-18
JP3188492B2 (ja)	2001-07-16
NO913788L (no)	1992-03-30
EP0483523A1 (en)	1992-05-06
CA2052347C (en)	2002-11-26
PT99082A (pt)	1992-08-31
FI108646B (fi)	2002-02-28
DK0483523T3 (da)	1997-06-16
AU650285B2 (en)	1994-06-16
CA2052347A1 (en)	1992-03-29
HUT59428A (en)	1992-05-28
CS297091A3 (en)	1992-04-15
HU211023B (en)	1995-09-28
KR100199685B1 (ko)	1999-06-15
JPH0625489A (ja)	1994-02-01
ATE147090T1 (de)	1997-01-15
ID960B (id)	1996-09-27
IT1243430B (it)	1994-06-10
TW212191B (fi)	1993-09-01
FI914524A0 (fi)	1991-09-26
HU913109D0 (en)	1992-01-28
DE69123935T2 (de)	1997-07-17

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NO308172B1 (no)	2000-08-07	Materiale av propylen-kopolymerer og fremgangsmÕte for fremstilling av dette
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