DE102010008854A1 - Stabilisatorsystem für verschäumbare halogenhaltige Polymere - Google Patents

Stabilisatorsystem für verschäumbare halogenhaltige Polymere Download PDF

Info

Publication number: DE102010008854A1
Authority: DE; Germany
Prior art keywords: acid; tert; butyl; bis; halogen
Prior art date: 2010-02-22
Legal status (The legal status 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 Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Withdrawn

Application number

DE102010008854A

Other languages

German (de)

English (en)

Inventor

Thomas 04155 Hillen

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Ika Innovative Kunststoffaufbereitung & Co KG GmbH

Ika Innovative Kunststoffaufbereitung & Co Kg 06766 GmbH

Ika Innovative Kunststoffaufbereitung & Co KG GmbH

Original Assignee

Ika Innovative Kunststoffaufbereitung & Co KG GmbH

Ika Innovative Kunststoffaufbereitung & Co Kg 06766 GmbH

Ika Innovative Kunststoffaufbereitung & Co KG GmbH

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.)

2010-02-22

Filing date

2010-02-22

Publication date

2011-08-25

2010-02-22 Application filed by Ika Innovative Kunststoffaufbereitung & Co KG GmbH, Ika Innovative Kunststoffaufbereitung & Co Kg 06766 GmbH, Ika Innovative Kunststoffaufbereitung & Co KG GmbH filed Critical Ika Innovative Kunststoffaufbereitung & Co KG GmbH

2010-02-22 Priority to DE102010008854A priority Critical patent/DE102010008854A1/de

2011-02-08 Priority to PCT/EP2011/051823 priority patent/WO2011101274A1/fr

2011-08-25 Publication of DE102010008854A1 publication Critical patent/DE102010008854A1/de

Status Withdrawn legal-status Critical Current

Links

229920000642 polymer Polymers 0.000 title claims abstract description 50
239000003381 stabilizer Substances 0.000 title claims abstract description 35
229910052736 halogen Inorganic materials 0.000 title claims abstract description 22
150000002367 halogens Chemical class 0.000 title claims abstract description 22
239000000203 mixture Substances 0.000 claims abstract description 74
239000004604 Blowing Agent Substances 0.000 claims abstract description 16
150000003752 zinc compounds Chemical class 0.000 claims abstract description 14
239000004088 foaming agent Substances 0.000 claims abstract description 10
150000007974 melamines Chemical class 0.000 claims abstract description 7
238000007664 blowing Methods 0.000 claims abstract description 5
-1 zinc carboxylate Chemical class 0.000 claims description 140
239000011734 sodium Substances 0.000 claims description 23
239000004800 polyvinyl chloride Substances 0.000 claims description 22
229920000915 polyvinyl chloride Polymers 0.000 claims description 22
239000011701 zinc Substances 0.000 claims description 19
239000006260 foam Substances 0.000 claims description 15
238000000034 method Methods 0.000 claims description 12
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JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 9
229910052725 zinc Inorganic materials 0.000 claims description 9
XOZUGNYVDXMRKW-AATRIKPKSA-N azodicarbonamide Chemical compound NC(=O)\N=N\C(N)=O XOZUGNYVDXMRKW-AATRIKPKSA-N 0.000 claims description 7
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150000001875 compounds Chemical class 0.000 description 34
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125000003118 aryl group Chemical group 0.000 description 6
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239000003380 propellant Substances 0.000 description 6
ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 6
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229910052801 chlorine Inorganic materials 0.000 description 5
GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical class [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
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OBETXYAYXDNJHR-UHFFFAOYSA-N 2-Ethylhexanoic acid Chemical class CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 4
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239000003963 antioxidant agent Substances 0.000 description 4
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125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 4
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XUQNLOIVFHUMTR-UHFFFAOYSA-N 2-[[2-hydroxy-5-nonyl-3-(1-phenylethyl)phenyl]methyl]-4-nonyl-6-(1-phenylethyl)phenol Chemical compound OC=1C(C(C)C=2C=CC=CC=2)=CC(CCCCCCCCC)=CC=1CC(C=1O)=CC(CCCCCCCCC)=CC=1C(C)C1=CC=CC=C1 XUQNLOIVFHUMTR-UHFFFAOYSA-N 0.000 description 3
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125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
GIPDEPRRXIBGNF-KTKRTIGZSA-N oxolan-2-ylmethyl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC1CCCO1 GIPDEPRRXIBGNF-KTKRTIGZSA-N 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
239000002245 particle Substances 0.000 description 1
HVINKLZTQUQDJO-UHFFFAOYSA-N pentadecane-2,4-dione Chemical compound CCCCCCCCCCCC(=O)CC(C)=O HVINKLZTQUQDJO-UHFFFAOYSA-N 0.000 description 1
125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-M phenolate Chemical compound [O-]C1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-M 0.000 description 1
229960000969 phenyl salicylate Drugs 0.000 description 1
125000004344 phenylpropyl group Chemical group 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical class OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
150000003022 phthalic acids Chemical class 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920002755 poly(epichlorohydrin) Polymers 0.000 description 1
229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920002857 polybutadiene Polymers 0.000 description 1
229920000223 polyglycerol Polymers 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
229920001195 polyisoprene Polymers 0.000 description 1
239000004926 polymethyl methacrylate Substances 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
ZUFQCVZBBNZMKD-UHFFFAOYSA-M potassium 2-ethylhexanoate Chemical compound [K+].CCCCC(CC)C([O-])=O ZUFQCVZBBNZMKD-UHFFFAOYSA-M 0.000 description 1
239000002243 precursor Substances 0.000 description 1
125000004368 propenyl group Chemical group C(=CC)* 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
150000003233 pyrroles Chemical class 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
239000002994 raw material Substances 0.000 description 1
239000012744 reinforcing agent Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
230000029058 respiratory gaseous exchange Effects 0.000 description 1
229960004889 salicylic acid Drugs 0.000 description 1
CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 description 1
150000003330 sebacic acids Chemical class 0.000 description 1
DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
229910052665 sodalite Inorganic materials 0.000 description 1
235000012217 sodium aluminium silicate Nutrition 0.000 description 1
125000004436 sodium atom Chemical group 0.000 description 1
150000003388 sodium compounds Chemical class 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
235000010199 sorbic acid Nutrition 0.000 description 1
239000004334 sorbic acid Substances 0.000 description 1
229940075582 sorbic acid Drugs 0.000 description 1
235000012424 soybean oil Nutrition 0.000 description 1
239000003549 soybean oil Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000004616 structural foam Substances 0.000 description 1
150000003440 styrenes Chemical class 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
125000004434 sulfur atom Chemical group 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
235000020357 syrup Nutrition 0.000 description 1
239000006188 syrup Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
238000005496 tempering Methods 0.000 description 1
KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 1
229940072958 tetrahydrofurfuryl oleate Drugs 0.000 description 1
UFDHBDMSHIXOKF-UHFFFAOYSA-N tetrahydrophthalic acid Natural products OC(=O)C1=C(C(O)=O)CCCC1 UFDHBDMSHIXOKF-UHFFFAOYSA-N 0.000 description 1
230000008646 thermal stress Effects 0.000 description 1
235000019303 thiodipropionic acid Nutrition 0.000 description 1
229910052718 tin Inorganic materials 0.000 description 1
239000010936 titanium Substances 0.000 description 1
150000004992 toluidines Chemical class 0.000 description 1
GTZCVFVGUGFEME-UHFFFAOYSA-N trans-aconitic acid Natural products OC(=O)CC(C(O)=O)=CC(O)=O GTZCVFVGUGFEME-UHFFFAOYSA-N 0.000 description 1
STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
229960001147 triclofos Drugs 0.000 description 1
FICPQAZLPKLOLH-UHFFFAOYSA-N tricyclohexyl phosphite Chemical compound C1CCCCC1OP(OC1CCCCC1)OC1CCCCC1 FICPQAZLPKLOLH-UHFFFAOYSA-N 0.000 description 1
150000005691 triesters Chemical class 0.000 description 1
QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
KOWVWXQNQNCRRS-UHFFFAOYSA-N tris(2,4-dimethylphenyl) phosphate Chemical compound CC1=CC(C)=CC=C1OP(=O)(OC=1C(=CC(C)=CC=1)C)OC1=CC=C(C)C=C1C KOWVWXQNQNCRRS-UHFFFAOYSA-N 0.000 description 1
125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229940005605 valeric acid Drugs 0.000 description 1
229920001567 vinyl ester resin Polymers 0.000 description 1
FUSUHKVFWTUUBE-UHFFFAOYSA-N vinyl methyl ketone Natural products CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
125000005023 xylyl group Chemical group 0.000 description 1
150000003751 zinc Chemical class 0.000 description 1
BOXSVZNGTQTENJ-UHFFFAOYSA-L zinc dibutyldithiocarbamate Chemical compound [Zn+2].CCCCN(C([S-])=S)CCCC.CCCCN(C([S-])=S)CCCC BOXSVZNGTQTENJ-UHFFFAOYSA-L 0.000 description 1

Classifications

- 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
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
- C08K5/098—Metal salts of carboxylic acids
- 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
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines

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)

DE102010008854A 2010-02-22 2010-02-22 Stabilisatorsystem für verschäumbare halogenhaltige Polymere Withdrawn DE102010008854A1 (de)

Priority Applications (2)

Application Number	Priority Date	Filing Date	Title
DE102010008854A DE102010008854A1 (de)	2010-02-22	2010-02-22	Stabilisatorsystem für verschäumbare halogenhaltige Polymere
PCT/EP2011/051823 WO2011101274A1 (fr)	2010-02-22	2011-02-08	Système stabilisateur pour polymères halogénés expansibles

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE102010008854A DE102010008854A1 (de)	2010-02-22	2010-02-22	Stabilisatorsystem für verschäumbare halogenhaltige Polymere

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Publication Number	Publication Date
DE102010008854A1 true DE102010008854A1 (de)	2011-08-25

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Country Status (2)

Country	Link
DE (1)	DE102010008854A1 (fr)
WO (1)	WO2011101274A1 (fr)

Citations (31)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE549340C (de)	1928-02-04	1932-04-26	Edeleanu Gmbh	Verfahren zur Entfernung von SO-Nebeln aus Gasgemischen
US4000100A (en)	1971-06-04	1976-12-28	W. R. Grace & Co.	Thermal and light stabilized polyvinyl chloride resins
DE2600516B2 (de)	1975-01-10	1978-04-13	Rhone-Poulenc Industries, Paris	Hitzestabilisierte Formmassen auf der Basis von Vinylchlorid Homopolymerisaten und Copolymerisaten
JPS54154441A (en)	1978-05-26	1979-12-05	Adeka Argus Chem Co Ltd	Halogen-containing resin composition
JPS5523121A (en)	1978-08-04	1980-02-19	Adeka Argus Chem Co Ltd	Halogen-containing resin composition
EP0022087A1 (fr)	1979-06-28	1981-01-07	Ciba-Geigy Ag	Stabilisants pour thermoplastes chlorés
EP0035268A1 (fr)	1980-03-03	1981-09-09	ADEKA ARGUS CHEMICAL CO., Ltd.	Composés organiques chlorés ayant une résistance élevée à la détérioration au moyen de composés 1,3-dicarbonylés
GB2078761A (en)	1980-06-27	1982-01-13	Ciba Geigy Ag	Pyrrole-stabilised chlorine-containing thermoplastics
EP0062813A1 (fr)	1981-04-03	1982-10-20	Henkel Kommanditgesellschaft auf Aktien	Masses moulées de chlorure de polyvinyl stabilisé
EP0282912A2 (fr)	1987-03-18	1988-09-21	BASF Lacke + Farben AG	Composition de stabilisants pour polymères de chlorure de vinyle
EP0307358A1 (fr)	1987-09-11	1989-03-15	Ciba-Geigy Ag	Dicétones-2,3 contenant des éthers ou des thioéthers et leur application comme stabilisants pour polymères chlorés
DE3843581A1 (de)	1987-12-29	1989-07-13	Nippon Synthetic Chem Ind	Halogen enthaltende thermoplastische harzzusammensetzung
DE4031818A1 (de)	1990-10-08	1992-04-09	Henkel Kgaa	Kationische schichtverbindungen
EP0506617A2 (fr)	1991-03-27	1992-09-30	Ciba-Geigy Ag	Agent durcisseur pour revêtements sous forme de poudre à base de polyesters
US5204393A (en) *	1991-09-05	1993-04-20	Hoechst Celanese Corporation	Three-component intumescent flame retardant
EP0549340A1 (fr)	1991-12-27	1993-06-30	Mizusawa Industrial Chemicals, Ltd.	Stabilisateur pour résines
WO1993020135A1 (fr)	1992-04-02	1993-10-14	Vista Chemical Company	Compositions stabilisantes pour des polymeres contenant de l'halogene, et compositions polymeres les contenant
JPH06192521A (ja)	1992-04-21	1994-07-12	Nisshin Fine Chem Kk	安定化されたハロゲン含有樹脂組成物
DE4425266C1 (de)	1994-07-16	1995-10-19	Metallgesellschaft Ag	Schichtgitterverbindungen und deren Verwendung
EP0761756A1 (fr)	1995-03-10	1997-03-12	Fuji Chemical Industry Co., Ltd.	Stabilisateur pour resines contenant de l'halogene et son procede de preparation, composition de resine contenant de l'halogene et sel d'hydroxyde composite
US6096820A (en)	1999-07-29	2000-08-01	Pq Corporation	Aluminosilicate stabilized halogenated polymers
US6531533B1 (en)	1995-06-30	2003-03-11	Crompton Vinyl Additives Gmbh	Stabilized halogen-containing polymers
DE10217364A1 (de)	2002-04-18	2003-10-30	Sued Chemie Ag	Verfahren zur Herstellung von Hydrotalciten
EP1088032B1 (fr)	1998-04-24	2004-01-21	Baerlocher GmbH	Association de stabilisants pour composition de resine thermoplastique halogenee
WO2005054358A1 (fr)	2003-12-04	2005-06-16	Reagens Deutschland Gmbh	Utilisation de compositions comprenant des isocyanurates et des (hydr)oxydes de magnesium pour stabiliser des matieres plastiques organiques contenant des halogenes
WO2006013040A2 (fr)	2004-07-30	2006-02-09	Artemis Research Gmbh & Co. Kg	Systeme de stabilisateur destine a des polymeres halogenes
WO2006136191A1 (fr)	2005-06-23	2006-12-28	Catena Additives Gmbh & Co. Kg	Complexes internes de triethanolaminoperchlorato(triflato)-metal polymeres de coordination utilises en tant qu'additifs pour des polymeres de synthese
DE102005038276A1 (de) *	2005-08-12	2007-02-15	Baerlocher Gmbh	Stabilisatorzusammensetzungen auf der Basis von Guanidin- oder Melamin-Verbindungen zur Stabilisierung halogenhaltiger Polymerer
DE102006055214A1 (de)	2006-11-21	2008-05-29	Nabaltec Gmbh	Kalzium-karbonato-hydroxodialuminate mit hexagonal-plättchenförmigen Kristallhabitus
DE102007050428A1 (de)	2007-10-22	2009-04-23	Catena Additives Gmbh & Co. Kg	Verfahren zur Herstellung eines Granulates ausgehend von Triethanlamin und einem Alkali- bzw. Erdalkaliperchlorat
EP2072567A1 (fr)	2007-12-18	2009-06-24	Bene_fit Systems GmbH & Co. KG	Composition destinée à la stabilisation de polymères contenant de l'halogène, son procédé de fabrication et d'utilisation

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5523121B2 (fr)	1973-08-04	1980-06-20
JPH0761756A (ja)	1993-08-31	1995-03-07	Toshiba Corp	車椅子兼用エスカレータの制御装置
WO2002062885A2 (fr) *	2000-11-03	2002-08-15	Cytec Technology Corp.	Articles polymeres contenant des photostabilisants a amine empechee formes a partir de composes carbonyle multi-fonctionnels
US6806304B2 (en) *	2001-09-27	2004-10-19	Cytec Technology Corp.	Process for improving the shelf life of a hindered phenol antioxidant
JP2006520260A (ja) *	2003-02-14	2006-09-07	エーブリー　デニソン　コーポレイション	ドライペイント移動ラミネートを作製する押出し成形方法
DE102007011553A1 (de) *	2007-03-09	2008-09-11	Chemetall Gmbh	Verfahren zur Beschichtung von metallischen Oberflächen mit einer wässerigen, Polymere enthaltenden Zusammensetzung, die wässerige Zusammensetzung und Verwendung der beschichteten Substrate
WO2010026230A1 (fr) *	2008-09-05	2010-03-11	Thor Gmbh	Composition retardatrice de flamme renfermant un dérivé de l'acide phosphonique

2010
- 2010-02-22 DE DE102010008854A patent/DE102010008854A1/de not_active Withdrawn
2011
- 2011-02-08 WO PCT/EP2011/051823 patent/WO2011101274A1/fr not_active Ceased

Patent Citations (32)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE549340C (de)	1928-02-04	1932-04-26	Edeleanu Gmbh	Verfahren zur Entfernung von SO-Nebeln aus Gasgemischen
US4000100A (en)	1971-06-04	1976-12-28	W. R. Grace & Co.	Thermal and light stabilized polyvinyl chloride resins
DE2600516B2 (de)	1975-01-10	1978-04-13	Rhone-Poulenc Industries, Paris	Hitzestabilisierte Formmassen auf der Basis von Vinylchlorid Homopolymerisaten und Copolymerisaten
JPS54154441A (en)	1978-05-26	1979-12-05	Adeka Argus Chem Co Ltd	Halogen-containing resin composition
JPS5523121A (en)	1978-08-04	1980-02-19	Adeka Argus Chem Co Ltd	Halogen-containing resin composition
EP0022087A1 (fr)	1979-06-28	1981-01-07	Ciba-Geigy Ag	Stabilisants pour thermoplastes chlorés
EP0035268A1 (fr)	1980-03-03	1981-09-09	ADEKA ARGUS CHEMICAL CO., Ltd.	Composés organiques chlorés ayant une résistance élevée à la détérioration au moyen de composés 1,3-dicarbonylés
GB2078761A (en)	1980-06-27	1982-01-13	Ciba Geigy Ag	Pyrrole-stabilised chlorine-containing thermoplastics
EP0062813A1 (fr)	1981-04-03	1982-10-20	Henkel Kommanditgesellschaft auf Aktien	Masses moulées de chlorure de polyvinyl stabilisé
EP0282912A2 (fr)	1987-03-18	1988-09-21	BASF Lacke + Farben AG	Composition de stabilisants pour polymères de chlorure de vinyle
EP0307358A1 (fr)	1987-09-11	1989-03-15	Ciba-Geigy Ag	Dicétones-2,3 contenant des éthers ou des thioéthers et leur application comme stabilisants pour polymères chlorés
DE3843581A1 (de)	1987-12-29	1989-07-13	Nippon Synthetic Chem Ind	Halogen enthaltende thermoplastische harzzusammensetzung
DE4031818A1 (de)	1990-10-08	1992-04-09	Henkel Kgaa	Kationische schichtverbindungen
EP0506617A2 (fr)	1991-03-27	1992-09-30	Ciba-Geigy Ag	Agent durcisseur pour revêtements sous forme de poudre à base de polyesters
US5204393A (en) *	1991-09-05	1993-04-20	Hoechst Celanese Corporation	Three-component intumescent flame retardant
EP0549340A1 (fr)	1991-12-27	1993-06-30	Mizusawa Industrial Chemicals, Ltd.	Stabilisateur pour résines
WO1993020135A1 (fr)	1992-04-02	1993-10-14	Vista Chemical Company	Compositions stabilisantes pour des polymeres contenant de l'halogene, et compositions polymeres les contenant
JPH06192521A (ja)	1992-04-21	1994-07-12	Nisshin Fine Chem Kk	安定化されたハロゲン含有樹脂組成物
DE4425266C1 (de)	1994-07-16	1995-10-19	Metallgesellschaft Ag	Schichtgitterverbindungen und deren Verwendung
EP0761756A1 (fr)	1995-03-10	1997-03-12	Fuji Chemical Industry Co., Ltd.	Stabilisateur pour resines contenant de l'halogene et son procede de preparation, composition de resine contenant de l'halogene et sel d'hydroxyde composite
US6531533B1 (en)	1995-06-30	2003-03-11	Crompton Vinyl Additives Gmbh	Stabilized halogen-containing polymers
EP1088032B1 (fr)	1998-04-24	2004-01-21	Baerlocher GmbH	Association de stabilisants pour composition de resine thermoplastique halogenee
US6096820A (en)	1999-07-29	2000-08-01	Pq Corporation	Aluminosilicate stabilized halogenated polymers
DE10217364A1 (de)	2002-04-18	2003-10-30	Sued Chemie Ag	Verfahren zur Herstellung von Hydrotalciten
WO2005054358A1 (fr)	2003-12-04	2005-06-16	Reagens Deutschland Gmbh	Utilisation de compositions comprenant des isocyanurates et des (hydr)oxydes de magnesium pour stabiliser des matieres plastiques organiques contenant des halogenes
WO2006013040A2 (fr)	2004-07-30	2006-02-09	Artemis Research Gmbh & Co. Kg	Systeme de stabilisateur destine a des polymeres halogenes
WO2006136191A1 (fr)	2005-06-23	2006-12-28	Catena Additives Gmbh & Co. Kg	Complexes internes de triethanolaminoperchlorato(triflato)-metal polymeres de coordination utilises en tant qu'additifs pour des polymeres de synthese
DE102005038276A1 (de) *	2005-08-12	2007-02-15	Baerlocher Gmbh	Stabilisatorzusammensetzungen auf der Basis von Guanidin- oder Melamin-Verbindungen zur Stabilisierung halogenhaltiger Polymerer
EP1913067A1 (fr)	2005-08-12	2008-04-23	Baerlocher GmbH	Compositions stabilisantes a base de composes de guanidine ou de melamine pour stabiliser des polymeres halogenes
DE102006055214A1 (de)	2006-11-21	2008-05-29	Nabaltec Gmbh	Kalzium-karbonato-hydroxodialuminate mit hexagonal-plättchenförmigen Kristallhabitus
DE102007050428A1 (de)	2007-10-22	2009-04-23	Catena Additives Gmbh & Co. Kg	Verfahren zur Herstellung eines Granulates ausgehend von Triethanlamin und einem Alkali- bzw. Erdalkaliperchlorat
EP2072567A1 (fr)	2007-12-18	2009-06-24	Bene_fit Systems GmbH & Co. KG	Composition destinée à la stabilisation de polymères contenant de l'halogène, son procédé de fabrication et d'utilisation

Non-Patent Citations (6)

* Cited by examiner, † Cited by third party
Title
"Plastics Additives Handbook" auf Seite 271, Kapitel 5.7.2
"Plastics Additives Handbook", Herausgeber H. Gächter und H. Müller, Hanser Publishers, 1985, Seite 284, Kapitel 5.7.10
"Plastics Additives Handbook", Herausgeber H. Gächter und H. Müller, Hanser Publishers, 1985, Seite 284, Kapitel 5.7.11 (Gruppe F)), und Kapitel 5.7.13 (Gruppe G))
"PVC Technology", Herausgeber W.V. Titow, 4th. Ed., Elsevier Publishers, 1984, Seite 171 bis 173, Kapitel 6.10.2 (Gruppe F)), Seite 174, Kapitel 6.10.5 (Gruppe G)), Seite 173, Kapitel 6.10.3 (Gruppe H)) und Seite 173 bis 174, Kapitel 6.10.4 (Gruppe I))
"PVC Technology", Herausgeber W.V., Titow, 4th. Ed., Elsevier Publ. 1984, Seite 165 bis 170
Hansjürgen Saechtling, Kunststoff-Taschenbuch, 22. Auflage, Carl Hanser Verlag München

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Publication number	Publication date
WO2011101274A1 (fr)	2011-08-25

Publication	Publication Date	Title
EP0625546B1 (fr)	1998-05-13	Chlorure de polyvinyle stabilisé
EP0677550B1 (fr)	1999-08-18	Polychlorure de vinyle stabilisé
EP1325941B1 (fr)	2005-06-01	Combinaisons de stabilisateurs pour les polymères chlorés
EP0716123B2 (fr)	2002-07-17	Chlorure de polyvinyle stabilisé
EP0930332B1 (fr)	2003-05-14	Système de stabilisateurs pour les polymères chlorés
EP0677551B1 (fr)	1999-08-25	PCV stabilisé souple
US6013703A (en)	2000-01-11	Stabilizer combination for chlorine-containing polymers
EP0751179B1 (fr)	2006-06-07	Polymères halogénés antistatiques
EP1510545A2 (fr)	2005-03-02	6-aminouraciles substitués en 1,3 pour stabiliser des polymères halogénés
EP1569994B1 (fr)	2008-01-09	6-amino-uraciles monosubstitues utilises pour stabiliser des polymeres a base d'halogenes
EP0421933B1 (fr)	1996-06-12	Compositions de polymères chlorés stabilisées
EP2110405B1 (fr)	2015-09-02	Systèmes de stabilisateur pour polymères contenant de l'halogène
AT413210B (de)	2005-12-15	Stabilisatorkombination für halogenhaltige polymere
EP0432096A1 (fr)	1991-06-12	Composition stabilisée contenant du chlore
US5804622A (en)	1998-09-08	Monomeric N-piperidinylmelamines as stabilizers for chlorine-containing polymers
DE102010008854A1 (de)	2011-08-25	Stabilisatorsystem für verschäumbare halogenhaltige Polymere
EP0796840A2 (fr)	1997-09-24	Stabilisateurs pour polymères contenant du chlore
GB2345696A (en)	2000-07-19	Stabilizer combinations for halogen-containing polymers
EP0682064A2 (fr)	1995-11-15	Polymères stabilisés contenant de l'halogène
WO2004018552A1 (fr)	2004-03-04	Utilisation de compositions contenant des 4-hydroxy-2-pyrones pour la stabilisation de plastiques organiques halogenes

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DE102010008854A1 - Stabilisatorsystem für verschäumbare halogenhaltige Polymere - Google Patents

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