NO309003B1 - Krystallinsk propylenpolymermateriale - Google Patents

Krystallinsk propylenpolymermateriale Download PDF

Info

Publication number: NO309003B1
Authority: NO; Norway
Prior art keywords: polymer material; propylene polymer; accordance; crystalline propylene; formula
Prior art date: 1995-04-05

Application number

NO961229A

Other languages

English (en)

Norwegian (no)

Other versions

NO961229D0 (no

NO961229L (no

Inventor

Tsutomu Nosu

Yoshiharu Sawa

Original Assignee

Kyowa Chem Ind Co Ltd

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.)

1995-04-05

Filing date

1996-03-27

Publication date

2000-11-27

1996-03-27 Application filed by Kyowa Chem Ind Co Ltd filed Critical Kyowa Chem Ind Co Ltd

1996-03-27 Publication of NO961229D0 publication Critical patent/NO961229D0/no

1996-10-07 Publication of NO961229L publication Critical patent/NO961229L/no

2000-11-27 Publication of NO309003B1 publication Critical patent/NO309003B1/no

Links

229920001155 polypropylene Polymers 0.000 title claims abstract description 33
239000002861 polymer material Substances 0.000 title claims description 19
-1 aromatic peroxide Chemical class 0.000 claims abstract description 38
229960001545 hydrotalcite Drugs 0.000 claims abstract description 24
229910001701 hydrotalcite Inorganic materials 0.000 claims abstract description 24
150000001450 anions Chemical class 0.000 claims abstract description 5
239000003054 catalyst Substances 0.000 claims description 9
239000000194 fatty acid Substances 0.000 claims description 9
235000014113 dietary fatty acids Nutrition 0.000 claims description 8
229930195729 fatty acid Natural products 0.000 claims description 8
150000004665 fatty acids Chemical class 0.000 claims description 6
229920001577 copolymer Polymers 0.000 claims description 4
229910052736 halogen Inorganic materials 0.000 claims description 4
150000002367 halogens Chemical class 0.000 claims description 4
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 4
239000007822 coupling agent Substances 0.000 claims description 3
229910052751 metal Inorganic materials 0.000 claims description 3
239000002184 metal Substances 0.000 claims description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 2
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 2
150000002500 ions Chemical class 0.000 claims description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
229920001384 propylene homopolymer Polymers 0.000 claims description 2
150000003839 salts Chemical class 0.000 claims description 2
239000011163 secondary particle Substances 0.000 claims description 2
229940095064 tartrate Drugs 0.000 claims description 2
239000000126 substance Substances 0.000 claims 1
239000000203 mixture Substances 0.000 abstract description 3
239000011347 resin Substances 0.000 description 15
229920005989 resin Polymers 0.000 description 15
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 13
239000000463 material Substances 0.000 description 11
239000008188 pellet Substances 0.000 description 9
230000002401 inhibitory effect Effects 0.000 description 6
239000003963 antioxidant agent Substances 0.000 description 5
CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 5
239000008116 calcium stearate Substances 0.000 description 5
235000013539 calcium stearate Nutrition 0.000 description 5
GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 description 5
229910000831 Steel Inorganic materials 0.000 description 4
230000003078 antioxidant effect Effects 0.000 description 4
230000015556 catabolic process Effects 0.000 description 4
230000000052 comparative effect Effects 0.000 description 4
238000006731 degradation reaction Methods 0.000 description 4
239000011777 magnesium Substances 0.000 description 4
238000000034 method Methods 0.000 description 4
239000010959 steel Substances 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
229910052782 aluminium Inorganic materials 0.000 description 3
239000000835 fiber Substances 0.000 description 3
239000007924 injection Substances 0.000 description 3
238000002347 injection Methods 0.000 description 3
150000002978 peroxides Chemical class 0.000 description 3
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
229910001209 Low-carbon steel Inorganic materials 0.000 description 2
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
239000000314 lubricant Substances 0.000 description 2
229910052749 magnesium Inorganic materials 0.000 description 2
YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 2
229920005629 polypropylene homopolymer Polymers 0.000 description 2
239000012756 surface treatment agent Substances 0.000 description 2
GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 2
239000011701 zinc Substances 0.000 description 2
239000004711 α-olefin Substances 0.000 description 2
WRXCBRHBHGNNQA-UHFFFAOYSA-N (2,4-dichlorobenzoyl) 2,4-dichlorobenzenecarboperoxoate Chemical compound ClC1=CC(Cl)=CC=C1C(=O)OOC(=O)C1=CC=C(Cl)C=C1Cl WRXCBRHBHGNNQA-UHFFFAOYSA-N 0.000 description 1
NLBJAOHLJABDAU-UHFFFAOYSA-N (3-methylbenzoyl) 3-methylbenzenecarboperoxoate Chemical compound CC1=CC=CC(C(=O)OOC(=O)C=2C=C(C)C=CC=2)=C1 NLBJAOHLJABDAU-UHFFFAOYSA-N 0.000 description 1
RIPYNJLMMFGZSX-UHFFFAOYSA-N (5-benzoylperoxy-2,5-dimethylhexan-2-yl) benzenecarboperoxoate Chemical compound C=1C=CC=CC=1C(=O)OOC(C)(C)CCC(C)(C)OOC(=O)C1=CC=CC=C1 RIPYNJLMMFGZSX-UHFFFAOYSA-N 0.000 description 1
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
BEQKKZICTDFVMG-UHFFFAOYSA-N 1,2,3,4,6-pentaoxepane-5,7-dione Chemical compound O=C1OOOOC(=O)O1 BEQKKZICTDFVMG-UHFFFAOYSA-N 0.000 description 1
XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 1
KRDXTHSSNCTAGY-UHFFFAOYSA-N 2-cyclohexylpyrrolidine Chemical compound C1CCNC1C1CCCCC1 KRDXTHSSNCTAGY-UHFFFAOYSA-N 0.000 description 1
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 1
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
239000004342 Benzoyl peroxide Substances 0.000 description 1
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
101100283604 Caenorhabditis elegans pigk-1 gene Proteins 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 1
239000005642 Oleic acid Substances 0.000 description 1
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 description 1
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
235000021355 Stearic acid Nutrition 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
239000002250 absorbent Substances 0.000 description 1
230000002745 absorbent Effects 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
230000003213 activating effect Effects 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001447 alkali salts Chemical class 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
239000002216 antistatic agent Substances 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
230000000740 bleeding effect Effects 0.000 description 1
229920001400 block copolymer Polymers 0.000 description 1
238000005266 casting Methods 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000003086 colorant Substances 0.000 description 1
238000004040 coloring Methods 0.000 description 1
SPTHWAJJMLCAQF-UHFFFAOYSA-M ctk4f8481 Chemical compound [O-]O.CC(C)C1=CC=CC=C1C(C)C SPTHWAJJMLCAQF-UHFFFAOYSA-M 0.000 description 1
239000012933 diacyl peroxide Substances 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
229920001038 ethylene copolymer Polymers 0.000 description 1
238000005187 foaming Methods 0.000 description 1
239000007789 gas Substances 0.000 description 1
BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
239000012433 hydrogen halide Substances 0.000 description 1
229910000039 hydrogen halide Inorganic materials 0.000 description 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000004611 light stabiliser Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000000155 melt Substances 0.000 description 1
238000000465 moulding Methods 0.000 description 1
229910052759 nickel Inorganic materials 0.000 description 1
239000002667 nucleating agent Substances 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
239000002530 phenolic antioxidant Substances 0.000 description 1
229920000098 polyolefin Polymers 0.000 description 1
229920005604 random copolymer Polymers 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
229910000077 silane Inorganic materials 0.000 description 1
239000011949 solid catalyst Substances 0.000 description 1
238000010186 staining Methods 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1
239000010936 titanium Substances 0.000 description 1
229910052719 titanium Inorganic materials 0.000 description 1
239000001993 wax Substances 0.000 description 1
238000004260 weight control Methods 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
- 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
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/14—Peroxides

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Compositions Of Macromolecular Compounds (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Processes Of Treating Macromolecular Substances (AREA)

NO961229A 1995-04-05 1996-03-27 Krystallinsk propylenpolymermateriale NO309003B1 (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP7103198A JPH08277351A (ja)	1995-04-05	1995-04-05	結晶性プロピレン重合体組成物

Publications (3)

Publication Number	Publication Date
NO961229D0 NO961229D0 (no)	1996-03-27
NO961229L NO961229L (no)	1996-10-07
NO309003B1 true NO309003B1 (no)	2000-11-27

Family

ID=14347830

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO961229A NO309003B1 (no)	1995-04-05	1996-03-27	Krystallinsk propylenpolymermateriale

Country Status (13)

Country	Link
US (1)	US5677364A (de)
EP (1)	EP0736572B1 (de)
JP (1)	JPH08277351A (de)
KR (1)	KR0179443B1 (de)
CN (1)	CN1099437C (de)
AT (1)	ATE168124T1 (de)
AU (1)	AU694331B2 (de)
DE (1)	DE69600400T2 (de)
DK (1)	DK0736572T3 (de)
ES (1)	ES2119545T3 (de)
MY (1)	MY116649A (de)
NO (1)	NO309003B1 (de)
TW (1)	TW374091B (de)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BR9806034A (pt) *	1997-07-21	2000-01-18	Bp Amoco Corp	Composto tipo hidrotálico, catalisador adequado para reformar um hidrocarboneto, e, processos de reformar um hidrocarboneto contendo oxigênio.
KR100450385B1 (ko) *	1997-10-21	2005-01-17	삼성아토피나주식회사	폴리프로필렌 필름용 조성물
US6964692B2 (en)	2001-02-09	2005-11-15	General Motors Corporation	Carbon monoxide adsorption for carbon monoxide clean-up in a fuel cell system
JP4193044B2 (ja) *	2003-03-28	2008-12-10	戸田工業株式会社	Ｍｇ−Ｚｎ−Ａｌ系ハイドロタルサイト型粒子粉末及び該Ｍｇ−Ｚｎ−Ａｌ系ハイドロタルサイト型粒子粉末を用いた樹脂組成物
CN109400782B (zh) *	2017-08-18	2021-06-01	中国石化扬子石油化工有限公司	一种制备高抗冲共聚聚丙烯的方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5580447A (en)	1978-12-14	1980-06-17	Kyowa Chem Ind Co Ltd	Prevention of rust, deterioration or coloring of polyolefin and composition
EP0416321B1 (de) *	1989-08-28	1994-11-09	Chisso Corporation	Kristalline Polyolefinmischung
JPH06107717A (ja) *	1992-10-01	1994-04-19	Kyowa Chem Ind Co Ltd	塩化ビニル系単量体の重合方法および塩化ビニル系重合体組成物
JP3284209B2 (ja) *	1992-12-01	2002-05-20	東ソー株式会社	熱可塑性エラストマー組成物

1995
- 1995-04-05 JP JP7103198A patent/JPH08277351A/ja active Pending
1996
- 1996-03-27 NO NO961229A patent/NO309003B1/no not_active IP Right Cessation
- 1996-03-28 MY MYPI96001155A patent/MY116649A/en unknown
- 1996-03-29 AU AU50416/96A patent/AU694331B2/en not_active Ceased
- 1996-03-29 US US08/624,107 patent/US5677364A/en not_active Expired - Lifetime
- 1996-04-01 TW TW085103820A patent/TW374091B/zh active
- 1996-04-02 KR KR1019960009917A patent/KR0179443B1/ko not_active Expired - Lifetime
- 1996-04-03 DK DK96302400T patent/DK0736572T3/da active
- 1996-04-03 ES ES96302400T patent/ES2119545T3/es not_active Expired - Lifetime
- 1996-04-03 AT AT96302400T patent/ATE168124T1/de not_active IP Right Cessation
- 1996-04-03 DE DE69600400T patent/DE69600400T2/de not_active Expired - Lifetime
- 1996-04-03 EP EP96302400A patent/EP0736572B1/de not_active Expired - Lifetime
- 1996-04-05 CN CN96104506A patent/CN1099437C/zh not_active Expired - Fee Related

Also Published As

Publication number	Publication date
JPH08277351A (ja)	1996-10-22
ES2119545T3 (es)	1998-10-01
DE69600400T2 (de)	1998-10-29
NO961229D0 (no)	1996-03-27
DK0736572T3 (da)	1998-11-16
AU5041696A (en)	1996-10-17
DE69600400D1 (de)	1998-08-13
ATE168124T1 (de)	1998-07-15
NO961229L (no)	1996-10-07
KR960037758A (ko)	1996-11-19
AU694331B2 (en)	1998-07-16
KR0179443B1 (ko)	1999-05-15
US5677364A (en)	1997-10-14
CN1099437C (zh)	2003-01-22
EP0736572A1 (de)	1996-10-09
TW374091B (en)	1999-11-11
MY116649A (en)	2004-03-31
EP0736572B1 (de)	1998-07-08
CN1136052A (zh)	1996-11-20

Publication	Publication Date	Title
US4284762A (en)	1981-08-18	Method for inhibiting corrosion-causing tendency and coloration of halogen-containing olefin resins with hydrotalcite
US5834541A (en)	1998-11-10	Olefin polymer composition having low smoke generation and fiber and film prepared therefrom
US4526916A (en)	1985-07-02	Cross-linkable polyethylene compositions
EP0052868A1 (de)	1982-06-02	Flammfeste Harzzusammensetzung und Flammschutzmittelzusammensetzung
EP0134405B1 (de)	1989-11-23	Vernetzbare Polyäthylen-Zusammensetzung
EP0366305B1 (de)	1994-05-18	Stabilisierte Polyäthylenzusammensetzung
CA1112013A (fr)	1981-11-10	Procede pour l'extrusion de compositions a base de polymeres d'alpha-olefines
EP0730001A1 (de)	1996-09-04	Stabilisatoren für Plastikmaterialien
CN107000408A (zh)	2017-08-01	挤出聚丙烯的方法
EP2090616B1 (de)	2012-10-03	Metalldeaktivierende Polymerzusammensetzung
NO309003B1 (no)	2000-11-27	Krystallinsk propylenpolymermateriale
US4900792A (en)	1990-02-13	Crosslinkable polyethylene composition
US4594382A (en)	1986-06-10	Thermally stabilized carboxyl-containing ethylene copolymers and preparation thereof
EP0301875B1 (de)	1994-02-02	Polyolefin-Zusammensetzung
JPH04348148A (ja)	1992-12-03	改質プロピレン系重合体組成物の製造方法
JPH0469657B2 (de)	1992-11-06
JPH07107111B2 (ja)	1995-11-15	安定性の改良されたポリオレフィン組成物
EP0054268B1 (de)	1985-01-09	Verfahren und Zusammensetzung zum Extrudieren von mittels Ziegler-Natta-Katalysatoren hergestellten Olefinpolymeren
EP0068851A1 (de)	1983-01-05	Metallsalze von gehinderten phenolischen Antioxydantien als Antigelkomponente in durch Übergangsmetalle katalysierten, Halogenidrückstände enthaltenden Olefinpolymeren
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