EP0817812A1 - Polyamides ignifuges - Google Patents
Polyamides ignifugesInfo
- Publication number
- EP0817812A1 EP0817812A1 EP96905736A EP96905736A EP0817812A1 EP 0817812 A1 EP0817812 A1 EP 0817812A1 EP 96905736 A EP96905736 A EP 96905736A EP 96905736 A EP96905736 A EP 96905736A EP 0817812 A1 EP0817812 A1 EP 0817812A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- polyamide
- polyamides
- phosphorus
- flame
- phosphorus compound
- Prior art date
- 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- Withdrawn
Links
- 239000004952 Polyamide Substances 0.000 title claims abstract description 47
- 229920002647 polyamide Polymers 0.000 title claims abstract description 47
- 239000003063 flame retardant Substances 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 13
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 claims description 10
- 239000003365 glass fiber Substances 0.000 claims description 7
- 239000000945 filler Substances 0.000 claims description 6
- 238000010276 construction Methods 0.000 claims description 5
- 238000009413 insulation Methods 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 4
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 claims description 3
- 239000000347 magnesium hydroxide Substances 0.000 claims description 3
- 229910001862 magnesium hydroxide Inorganic materials 0.000 claims description 3
- ZQKXQUJXLSSJCH-UHFFFAOYSA-N melamine cyanurate Chemical compound NC1=NC(N)=NC(N)=N1.O=C1NC(=O)NC(=O)N1 ZQKXQUJXLSSJCH-UHFFFAOYSA-N 0.000 claims description 2
- XFZRQAZGUOTJCS-UHFFFAOYSA-N phosphoric acid;1,3,5-triazine-2,4,6-triamine Chemical compound OP(O)(O)=O.NC1=NC(N)=NC(N)=N1 XFZRQAZGUOTJCS-UHFFFAOYSA-N 0.000 claims description 2
- DXZMANYCMVCPIM-UHFFFAOYSA-L zinc;diethylphosphinate Chemical compound [Zn+2].CCP([O-])(=O)CC.CCP([O-])(=O)CC DXZMANYCMVCPIM-UHFFFAOYSA-L 0.000 claims description 2
- 229910052698 phosphorus Inorganic materials 0.000 abstract description 24
- 239000011574 phosphorus Substances 0.000 abstract description 24
- 239000000203 mixture Substances 0.000 abstract description 19
- -1 phosphorus compound Chemical class 0.000 abstract description 18
- 229920006018 co-polyamide Polymers 0.000 abstract 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 16
- 229920000642 polymer Polymers 0.000 description 11
- 238000004519 manufacturing process Methods 0.000 description 7
- 150000003018 phosphorus compounds Chemical class 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 238000004870 electrical engineering Methods 0.000 description 5
- 238000012545 processing Methods 0.000 description 5
- 229920002292 Nylon 6 Polymers 0.000 description 4
- 229920002302 Nylon 6,6 Polymers 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 150000002366 halogen compounds Chemical class 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 3
- 238000004898 kneading Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 150000007974 melamines Chemical class 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- YCGKJPVUGMBDDS-UHFFFAOYSA-N 3-(6-azabicyclo[3.1.1]hepta-1(7),2,4-triene-6-carbonyl)benzamide Chemical compound NC(=O)C1=CC=CC(C(=O)N2C=3C=C2C=CC=3)=C1 YCGKJPVUGMBDDS-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 229920000305 Nylon 6,10 Polymers 0.000 description 1
- 229920000572 Nylon 6/12 Polymers 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 description 1
- 230000000711 cancerogenic effect Effects 0.000 description 1
- 231100000315 carcinogenic Toxicity 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229940125898 compound 5 Drugs 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
- 238000007323 disproportionation reaction Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000005538 encapsulation Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000003203 everyday effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- BICAGYDGRXJYGD-UHFFFAOYSA-N hydrobromide;hydrochloride Chemical compound Cl.Br BICAGYDGRXJYGD-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 239000012764 mineral filler Substances 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 229910017464 nitrogen compound Inorganic materials 0.000 description 1
- 150000002830 nitrogen compounds Chemical class 0.000 description 1
- 150000002896 organic halogen compounds Chemical class 0.000 description 1
- 238000002161 passivation Methods 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000933 poly (ε-caprolactam) Polymers 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 229920006012 semi-aromatic polyamide Polymers 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
- 150000003752 zinc compounds Chemical class 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/53—Phosphorus bound to oxygen bound to oxygen and to carbon only
- C08K5/5397—Phosphine oxides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/48—Polymers modified by chemical after-treatment
-
- 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
-
- 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/521—Esters of phosphoric acids, e.g. of H3PO4
-
- 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/529—Esters containing heterocyclic rings not representing cyclic esters of phosphoric or phosphorous 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/53—Phosphorus bound to oxygen bound to oxygen and to carbon only
- C08K5/5317—Phosphonic compounds, e.g. R—P(:O)(OR')2
- C08K5/5333—Esters of phosphonic acids
- C08K5/5373—Esters of phosphonic acids containing heterocyclic rings not representing cyclic esters of phosphonic 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
- C08K5/49—Phosphorus-containing compounds
- C08K5/5398—Phosphorus bound to sulfur
Definitions
- the invention relates to a method for producing flame-retardant polyamides.
- PA Synthetic polyamides
- PA 6 poly- ⁇ -caprolactam
- PA 66 polyhexamethylene adipamide
- PA 11 polyundecanamide
- PA 12 poly- ⁇ -laurine lactam
- PA 610 polyhexamethylene sebacin amide
- PA 612 polyhexamethylene dodecanamide
- polyamides are self-extinguishing, but they lose this property after the addition of fillers such as glass fibers or pigments.
- fillers such as glass fibers or pigments.
- flame retardant is becoming increasingly popular Polyamide needed. In the event of a fire, the flame protection should provide sufficient time to save people and property.
- halogen compounds are predominantly chlorinated or broken hydrocarbons, which are often combined with zinc compounds or the synergistically effective antimony trioxide, which is carcinogenic in animal experiments.
- the halogen compounds have the disadvantage of releasing highly corrosive and highly toxic decomposition products, such as hydrogen chloride and hydrogen bromide, in the event of a fire and causing a strong smoke formation; they also reduce the toughness and the tracking resistance of the polyamides.
- Red phosphorus is mostly used in an encapsulated form. Despite the encapsulation, there is a risk of phosphorus fires at the high processing temperatures.
- This is achieved according to the invention in that a polyamide, a copolyamide or a polyamide blend at elevated temperature with a monoepoxy-functional phosphorus compound of the structure
- R 1 and R 2 alkyl, O-alkyl or S-alkyl, each with
- the phosphorus compound is chemically anchored to the polymer chain. Therefore can be obtained by a simple process phosphor-modified polyamides which - without halogen or red phosphorus - are sufficiently difficult to burn and meet all technical requirements. It has also been shown that the flame resistance that can be achieved depends solely on the amount of phosphorus anchored to the polymer chain.
- the method according to the invention which takes place at elevated temperature, i.e. generally at a temperature> 150 ° C (upper limit: ⁇ 350 ° C), can be carried out in known heatable mixing devices, such as kneaders, roller mixers and extruders. It is possible both to prepare premixes from the polyamide and the phosphorus compound, for example in a drum mixer or a fluid mixer, and to meter the phosphorus compound directly into the melt of the polyamide, to distribute it therein and to react it with the polyamide, i.e. to anchor on the polymer chain. In order to avoid evaporation losses when adding the phosphorus compound, it has proven to be advantageous to use phosphorus compounds with a molecular weight> 150.
- additives such as fillers, in particular glass fibers, as well as dyes, anti-aging agents, processing aids, etc.
- fillers in particular glass fibers, as well as dyes, anti-aging agents, processing aids, etc.
- dyes can also be used.
- the additives can also be mixed in beforehand or in a subsequent mixing process.
- the polyamide blend may advantageously additionally contain other halogen-free flame retardants are added.
- Mela incyanura, melamine phosphate and magnesium hydroxide are preferably used as such flame retardants.
- the amount of phosphorus compound required for flame-retardant adjustment of the polyamides depends on their chemical structure and the additives.
- the polyamides PA 6 and PA 66 require less phosphorus than the polyamides PA 11 and PA 12.
- polyamide mixtures with a high proportion of filler, such as glass fibers require higher phosphorus concentrations than filler-free mixtures.
- the required phosphorus content is therefore between 1 and 5% by mass, based on the polyamide mixture. Since the flame resistance of the polyamides depends solely on the phosphorus concentration in the polymer matrix, different amounts of phosphorus compound are required accordingly.
- the required proportion is - depending on the need and the phosphorus content of the phosphorus compound - 5 to 35% by mass, based on the polyamide mixture.
- the polymer modification can be carried out very simply and inexpensively in a mixing or extrusion process, as is required in any case for the homogenization of the polyamides after production or during their compounding for various technical purposes;
- the polyamides contain no volatile components, so that when used in electrical engineering and electronics there is no damage or passivation of electrical contacts; - No corrosive components are released from the polyamides;
- the polyamides are recyclable.
- the flame-retardant polyamides produced in accordance with the method according to the invention are advantageously suitable as insulation, construction and housing materials in electrical engineering and electronics.
- Other areas of application include, among others, automobile construction, the packaging industry, and machine and apparatus construction.
- the following components are used to manufacture polyamide molding compounds.
- Component A polyamide 6 with a relative viscosity ⁇ re ] _ of 2.9 (measured as a 0.5% solution in 96% H S0 4 according to ISO 307)
- Component B polyamide 66 with a relative viscosity ⁇ re ⁇ of 2.7
- Component C melamine cyanurate
- Component D glass fibers with an average diameter of
- components C and D are added — simultaneously or in succession, and then kneading is continued for at least 5 minutes. After the kneading process has ended, the mixture is discharged from the kneader and cooled. The cooled melt is then ground and sprayed into shaped bodies. The flame resistance according to UL 94 V (1.6 mm thick test bars), the modulus of elasticity according to DIN 53457 and the impact resistance according to DIN 53453 are measured on the shaped bodies. The values obtained are shown in Table 2.
- polyamide 6 listed in Table 2 (component A) are premixed with the specified parts by weight of the phosphorus compound V or VI in a drum mixer or stirred kettle at 100 to 150 ° C. and then in one
- Double-shaft extruder (ZSK 32, Werner and Pfleiderer) mixed at 300 ° C melt temperature, extruded into a water bath, crushed, dried and sprayed into shaped bodies. The results are summarized in Table 2. Table 1
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polyamides (AREA)
Abstract
Pour produire des polyamides ignifuges, on fait réagir, à haute température, un polyamide, un co-polyamide ou un mélange de polyamides avec un composé du phosphore à fonction monoépoxy, la quantité du composé de phosphore représentant 5 à 35 % de la masse totale, c'est-à-dire du mélange à base de polyamide.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19512175 | 1995-03-31 | ||
| DE19512175 | 1995-03-31 | ||
| PCT/DE1996/000465 WO1996030441A1 (fr) | 1995-03-31 | 1996-03-15 | Polyamides ignifuges |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP0817812A1 true EP0817812A1 (fr) | 1998-01-14 |
Family
ID=7758487
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP96905736A Withdrawn EP0817812A1 (fr) | 1995-03-31 | 1996-03-15 | Polyamides ignifuges |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US5942584A (fr) |
| EP (1) | EP0817812A1 (fr) |
| JP (1) | JPH11502554A (fr) |
| KR (1) | KR19980703312A (fr) |
| WO (1) | WO1996030441A1 (fr) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9609606D0 (en) | 1996-05-08 | 1996-07-10 | T & N Technology Ltd | Fire-resistant monofilament |
| GB2312900B (en) * | 1996-05-08 | 2000-03-29 | T & N Technology Ltd | Flame-retardant monofilament |
| JP4535557B2 (ja) * | 2000-03-31 | 2010-09-01 | 旭化成ケミカルズ株式会社 | 難燃性強化ポリアミド樹脂組成物 |
| DE10051051A1 (de) * | 2000-10-14 | 2002-04-18 | Bosch Gmbh Robert | Silikonmodifizierte Einkomponentenvergußmasse |
| DE10151955A1 (de) | 2001-10-22 | 2003-05-08 | Bosch Gmbh Robert | Massereduzierter Magnetspulenträger |
| DE102008050371B3 (de) * | 2008-10-02 | 2010-04-01 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | 1,2-Epoxypropylphosphonsäure und ihre Derivate für flammgeschützte Kunststoffe |
| US20110196052A1 (en) * | 2010-02-05 | 2011-08-11 | Basf Se | Flame retardants |
| RU2012137686A (ru) * | 2010-02-05 | 2014-03-10 | Басф Се | Огнезащитное средство |
| DE102010015155A1 (de) * | 2010-04-16 | 2011-10-20 | Schaeffler Technologies Gmbh & Co. Kg | Elektrisch isolierender Lagerring, insbesondere für ein Wälzlager |
| JP2014055209A (ja) * | 2012-09-11 | 2014-03-27 | Fuji Xerox Co Ltd | ポリ乳酸、樹脂組成物、および樹脂成形体 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0589284A1 (fr) * | 1992-09-24 | 1994-03-30 | Basf Corporation | Polyamide thermoplastique à inflammabilité réduite |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2856369A (en) * | 1953-05-08 | 1958-10-14 | Shell Dev | Epoxy-substituted esters of phosphoruscontaining acid and their polymers |
| BE755459A (fr) * | 1969-08-28 | 1971-03-01 | Knapsack Ag | Oxydes d'epoxyalkylphosphines et leur preparation |
| DE3609341A1 (de) * | 1986-03-20 | 1987-09-24 | Bayer Ag | Flammfeste, glasfaserverstaerkte polyamidformmassen |
| EP0242732B1 (fr) * | 1986-04-22 | 1992-01-08 | Bayer Ag | Polyamides ignifugés |
| DE3722118A1 (de) * | 1987-07-03 | 1989-01-12 | Brueggemann L Kg | Selbstverloeschende thermoplastische massen aus polykondensationsprodukten |
| DE3909145A1 (de) * | 1989-03-21 | 1990-09-27 | Basf Ag | Flammgeschuetzte polyamidformmassen auf der basis von cyanguanidin |
| DE4141861A1 (de) * | 1991-12-18 | 1993-06-24 | Du Pont Int | Flammwidrige polyamide |
| US5476887A (en) * | 1991-12-18 | 1995-12-19 | E. I. Du Pont De Nemours & Company | Flame retardant polyamides |
-
1996
- 1996-03-15 WO PCT/DE1996/000465 patent/WO1996030441A1/fr not_active Ceased
- 1996-03-15 JP JP8528760A patent/JPH11502554A/ja active Pending
- 1996-03-15 EP EP96905736A patent/EP0817812A1/fr not_active Withdrawn
- 1996-03-15 KR KR1019970706716A patent/KR19980703312A/ko not_active Withdrawn
- 1996-03-15 US US08/930,521 patent/US5942584A/en not_active Expired - Fee Related
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0589284A1 (fr) * | 1992-09-24 | 1994-03-30 | Basf Corporation | Polyamide thermoplastique à inflammabilité réduite |
Also Published As
| Publication number | Publication date |
|---|---|
| WO1996030441A1 (fr) | 1996-10-03 |
| JPH11502554A (ja) | 1999-03-02 |
| US5942584A (en) | 1999-08-24 |
| KR19980703312A (ko) | 1998-10-15 |
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