EP0297241A2 - Electrical insulating parts - Google Patents
Electrical insulating parts Download PDFInfo
- Publication number
- EP0297241A2 EP0297241A2 EP19880106680 EP88106680A EP0297241A2 EP 0297241 A2 EP0297241 A2 EP 0297241A2 EP 19880106680 EP19880106680 EP 19880106680 EP 88106680 A EP88106680 A EP 88106680A EP 0297241 A2 EP0297241 A2 EP 0297241A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- electrical insulating
- insulating parts
- parts according
- group
- polyester resin
- 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- Withdrawn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
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B7/00—Insulated conductors or cables characterised by their form
- H01B7/17—Protection against damage caused by external factors, e.g. sheaths or armouring
- H01B7/29—Protection against damage caused by extremes of temperature or by flame
- H01B7/295—Protection against damage caused by extremes of temperature or by flame using material resistant to flame
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
- H01B3/302—Polyurethanes or polythiourethanes; Polyurea or polythiourea
Definitions
- the invention relates to electrical insulating parts according to the preamble of claim 1 and in particular sheaths for electrical conductors and cables.
- polyesters with good electrical insulation properties are particularly suitable.
- the insulating material can be pulled as a hose over an electrical cable or sprayed directly onto the part to be insulated. It is also possible to wind the insulating material around the electrical conductor in the form of a film. The film is wound in several layers on top of one another in order to achieve the best possible electrical insulation. If a polyester film is used, the individual layers cannot be welded and cannot be connected to one another. A coating with additives that have high cohesive forces is therefore necessary in order to be able to mechanically connect the individual wound film layers to one another.
- this film is provided with stabilizers or anti-aging agents. It is also known to add color additives to the polyester film.
- the polyester film Since the polyester film is highly flammable and flammable, it is equipped with flame retardant or flame retardant agents.
- Technically important flame retardants included at least one of the following: Phosphorus, antimony, chlorine, bromine or nitrogen.
- Known flame retardants for plastics are chlorinated paraffins, highly chlorinated bicyclic compounds and bromine compounds.
- the organic halogen compounds are always used together with antimony trioxide.
- Inorganic phosphorus compounds, organic phosphonic acids or halogenated phosphorus compounds are also frequently found in flame retardants for plastics.
- the invention has for its object to make available electrical insulating parts which are provided with a flame-retardant coating.
- the flame-retardant coating is not intended to impair the Properties of the insulating material.
- Another object of the invention is to use connections for a flame-resistant coating, that do not lead to toxic or corrosive products in the event of fire.
- the electrical insulating parts which are produced from the polyester film and the halogen-free crosslinkable coating according to the invention are distinguished by improved mechanical properties, greatly reduced smoke density and by a better adhesive bond between the individual wound polyester layers. Comprehensive safety is achieved when this coating is applied to the polyester, since the toxicity and corrosiveness of the flue gases are significantly reduced in the event of a fire.
- the electrical insulating parts according to the invention are made of polyester, preferably in the form of a film, and a flame-retardant coating which contains a crosslinked halogen-free mixture of unsaturated polyester resin, crosslinking agents or chain extenders, catalysts, stabilizers or antiaging agents, dyes and flame retardants.
- the electrical parts insulated with the polyester film and the halogen-free coating are characterized by high abrasion resistance, notch resistance, dielectric strength, tensile strength and temperature resistance up to approximately 150 ° C.
- the additives of the coating do not have to be added in a significantly increased concentration in order to lead to sufficient flame retardancy.
- the above-described disadvantages of reduced flame retardancy or reduced strength are eliminated by using different combinations of flame retardants from two different connecting groups.
- the first linking group contains inorganic phosphate esters, phosphonated polyols, red phosphorus and organic phosphates.
- organic phosphates alkyl phosphates, allyl phosphates, aryl phosphates and in particular trioctyl phosphate, cresyl phosphate, phenyl phosphate, cresyl phenyl phosphate and ethyl acetyl hydroxybenzyl phosphate are preferably used. Connections from this first group are combined with connections from a second group.
- This second group of compounds contains boric acid, ammonium sulfonamides, inorganic phosphates, polyphosphates, borates and metal hydroxides.
- Particularly suitable borates are barium metaborates, zinc borates and ammonium borates; metal hydroxides which are preferably used are aluminum and magnesium hydroxides.
- Suitable inorganic phosphates include boron phosphates, and polyphosphates include ammonium polyphosphates.
- the improved flame retardancy is based on a synergistic effect of the flame protection system produced from the two groups mentioned. It is therefore not necessary to increase the dosage of the flame retardants.
- the amount of flame retardants from the first group is in the range from 0 to 80% by weight, the amount of flame retardants from the second group in the range from 0 to 70% by weight. Even small amounts of flame retardants from these two groups are sufficient to achieve high flame retardancy. Preferably 10-40% by weight of flame retardants from the first group and 20-60% by weight of flame retardants from the second group are used.
- the unsaturated polyester resin is made from terephthalic acid, aminocarboxylic acid or ⁇ -aminolauric acid.
- Preferred aryl or alkyl diisocyanates are toluyl isocyanate, 4,4'-methylene di (phenyl isocyanate), naphthalene-1, 5 or naphthalene, 1,4-diisocyanate, methylene tri (phenyl isocyanate) or hexamethylene diisocyanate.
- One or more of the compounds from the group of amines, hydrides, metal oxides, caroxylates, organometallic compounds or tetramethylbutane diamine, diazobicyclooctane, dibutyltin dilaurate or tin octate can be selected as the catalyst for the crosslinking reaction.
- Compounds of the mononuclear or polynuclear phenols substituted in the ortho or para position, the bisbenzooxazoles, the coumarin derivatives, polycarbodiimides, the aromatic amines, thioethers or the phosphites are preferably selected as stabilizers or anti-aging agents. The addition of these substances avoids the undesirable change in the chemical and physical structure of the insulating part during use.
- colorants on an inorganic or organic basis are used.
- suitable inorganic compounds are titanium dioxide, carbon black, iron oxide, chromium oxide, mixed oxides or spinel compounds
- suitable organic-based dyes are the azo dyes, phthalocyanines or dioxazines.
- lubricants are added to the coating.
- Suitable compounds are olefinic ketones or compounds based on wax, soap or oil.
Landscapes
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Organic Insulating Materials (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Laminated Bodies (AREA)
Abstract
Description
Die Erfindung betrifft elektrische Isolierteile gemäß dem Oberbegriff des Anspruchs 1 und insbesondere Umhüllungen für elektrische Leiter und Kabel.The invention relates to electrical insulating parts according to the preamble of claim 1 and in particular sheaths for electrical conductors and cables.
Verschiedene Kunststoffarten werden als Isoliermaterial für elektrische Bauteile verwendet. Besonders geeignet sind Polyester, die gute elektrische Isoliereigenschaften aufweisen. Das Isoliermaterial kann als Schlauch über ein elektrisches Kabel gezogen werden oder direkt auf das zu isolierende Teil aufgespritzt werden. Ebenso ist es möglich, den Isolierwerkstoff in Form einer Folie bzw. eines Films um den elektrischen Leiter zu wickeln. Dabei wird die Folie in mehreren Lagen übereinander gewickelt, um so eine möglichst gute elektrische Isolierung zu erreichen. Wird eine Polyesterfolie verwendet, lassen sich die einzelnen Lagen nicht verschweißen und nicht untereinander verbinden. Daher ist eine Beschichtung mit Zusatzstoffen notwendig, die hohe Kohäsionskräfte besitzen, um die einzelnen gewickelten Folienlagen miteinander mechanisch verbinden zu können.Various types of plastic are used as insulation material for electrical components. Polyesters with good electrical insulation properties are particularly suitable. The insulating material can be pulled as a hose over an electrical cable or sprayed directly onto the part to be insulated. It is also possible to wind the insulating material around the electrical conductor in the form of a film. The film is wound in several layers on top of one another in order to achieve the best possible electrical insulation. If a polyester film is used, the individual layers cannot be welded and cannot be connected to one another. A coating with additives that have high cohesive forces is therefore necessary in order to be able to mechanically connect the individual wound film layers to one another.
Um das Altern oder Brüchigwerden der Polyesterfolie zu verhindern oder erheblich zu verlangsamen, wird diese Folie mit Stabilisatoren bzw. Alterungsschutzmitteln versehen. Weiterhin ist es bekannt, die Polyesterfolie mit Farbzusätzen zu versehen.In order to prevent or considerably slow down the aging or breakage of the polyester film, this film is provided with stabilizers or anti-aging agents. It is also known to add color additives to the polyester film.
Da die Polyesterfolie leicht entzündlich und brennbar ist, wird sie mit flammhemmenden bzw. -widrigen Mitteln ausgerüstet. Technisch wichtige Flammschutzmittel enthalten mindestens eines der folgenden Elemente:
Phosphor, Antimon, Chlor, Brom oder Stickstoff. Bekannte Flammschutzmittel für Kunststoffe sind chlorierte Paraffine, hochchlorierte bicyklische Verbindungen und Bromverbindungen. Die organischen Halogenverbindungen werden immer zusammen mit Antimontrioxid angewandt. Auch anorganische Phosphorverbindungen, organische Phosphonsäuren oder halogenierte Phosphorverbindungen sind in Flammschutzmitteln für Kunststoffe häufig anzutreffen.Since the polyester film is highly flammable and flammable, it is equipped with flame retardant or flame retardant agents. Technically important flame retardants included at least one of the following:
Phosphorus, antimony, chlorine, bromine or nitrogen. Known flame retardants for plastics are chlorinated paraffins, highly chlorinated bicyclic compounds and bromine compounds. The organic halogen compounds are always used together with antimony trioxide. Inorganic phosphorus compounds, organic phosphonic acids or halogenated phosphorus compounds are also frequently found in flame retardants for plastics.
Allerdings ist der Einsatz von solchen Flammschutzmitteln in Kunststoffen insofern nachteilig, als die halogenierten Flammschutzmittel bei der Verbrennung die Atmosphäre belasten und toxische und stark korrodierende Wirkungen besitzen.However, the use of such flame retardants in plastics is disadvantageous in that the halogenated flame retardants pollute the atmosphere during combustion and have toxic and highly corrosive effects.
Es besteht daher ein Bedürfnis an flammwidrigen Beschichtungen für Isoliermaterialien interessiert, die halogenfrei sind. Es werden bereits einige halogenfreie Flammschutzmittel eingesetzt. Jedoch haben diese den Nachteil, daß die Menge an Flammschutzmittel beträchtlich erhöht werden muß, um die gleiche flammhemmende Wirkung zu erbringen wie die halogenhaltigen Flammschutzmittel. Die Forderung nach Schwerentflammbarkeit führt in diesen Fällen zu einem Verzicht auf einige der typischen Eigenschaften, zum Beispiel der Güte der mechanischen Eigenschaften.There is therefore a need for flame retardant coatings for insulating materials that are halogen free. Some halogen-free flame retardants are already used. However, these have the disadvantage that the amount of flame retardant must be increased considerably in order to produce the same flame retardant effect as the halogen-containing flame retardants. In these cases, the requirement for flame retardancy means that some of the typical properties, for example the quality of the mechanical properties, are dispensed with.
Der Erfindung liegt die Aufgabe zugrunde, elektrische Isolierteile verfügbar zu machen, die mit einer flammwidrigen Beschichtung versehen sind. Die flammwidrige Beschichtung soll dabei nicht zu einer Beeinträchtigung der
Eigenschaften des Isoliermaterials führen.The invention has for its object to make available electrical insulating parts which are provided with a flame-retardant coating. The flame-retardant coating is not intended to impair the
Properties of the insulating material.
Eine weitere Aufgabe der Erfindung ist es, Verbindungen für eine flammfeste Beschichtung zu verwenden, die im Brandfall nicht zu toxischen oder korrodierend wirkenden Produkten führen.Another object of the invention is to use connections for a flame-resistant coating, that do not lead to toxic or corrosive products in the event of fire.
Eine Lösung dieser Aufgabe ist im Anspruch 1 angegeben und kann den weiteren Ansprüchen gemäß vorteilhaft weitergebildet werden.A solution to this problem is specified in claim 1 and can advantageously be developed according to the other claims.
Die elektrischen Isolierteile, die aus der Polyesterfolie und der erfindungsgemäßen halogenfreien vernetzbaren Beschichtung hergestellt sind, zeichnen sich durch verbesserte mechanische Eigenschaften, stark verminderte Rauchgasdichte und durch eine bessere adhäsive Verbindung der einzelnen gewickelten Polyesterlagen aus. Bei Anwendung dieser Beschichtung auf dem Polyester wird eine umfassende Sicherheit erreicht, da im Brandfall die Toxizität und die Korrosivität der Rauchgase erheblich vermindert wird.The electrical insulating parts which are produced from the polyester film and the halogen-free crosslinkable coating according to the invention are distinguished by improved mechanical properties, greatly reduced smoke density and by a better adhesive bond between the individual wound polyester layers. Comprehensive safety is achieved when this coating is applied to the polyester, since the toxicity and corrosiveness of the flue gases are significantly reduced in the event of a fire.
Die erfindungsgemäßen elektrischen Isolierteile sind aus Polyester, vorzugsweise in Folienform, und einer flammwidrigen Beschichtung hergestellt, die eine vernetzte halogenfreie Mischung von ungesättigtem Polyesterharz, Vernetzern bzw. Kettenverlängerern, Katalysatoren, Stabilisatoren bzw. Alterungsschutzmitteln, Farbstoffen und Flammschutzmitteln enthält.The electrical insulating parts according to the invention are made of polyester, preferably in the form of a film, and a flame-retardant coating which contains a crosslinked halogen-free mixture of unsaturated polyester resin, crosslinking agents or chain extenders, catalysts, stabilizers or antiaging agents, dyes and flame retardants.
Die mit der Polyesterfolie und der halogenfreien Beschichtung isolierten elektrischen Teile, insbesondere elektrische Leiter und Kabel zeichnen sich durch hohe Abriebfestigkeit, Kerbfestigkeit, Spannungsfestigkeit, Zugfestigkeit und Temperaturbeständigkeit bis etwa 150° C aus. Die Zusatzstoffe der Beschichtung müssen nicht in einer wesentlich erhöhten Konzentration zugegeben werden, um zu einer ausreichenden Flammwidrigkeit zu führen.The electrical parts insulated with the polyester film and the halogen-free coating, in particular electrical conductors and cables, are characterized by high abrasion resistance, notch resistance, dielectric strength, tensile strength and temperature resistance up to approximately 150 ° C. The additives of the coating do not have to be added in a significantly increased concentration in order to lead to sufficient flame retardancy.
Die oben beschriebenen Nachteile einer verminderten Flammschutzwirkung bzw. einer verminderten Festigkeit werden durch die Verwendung verschiedener Kombinationen von Flammschutzmitteln aus zwei unterschiedlichen Verbindungsgruppen eliminiert. Die erste Verbindungsgruppe enthält anorganische Phosphatester, phosphonierte Polyole, roten Phosphor und organische Phosphate. Von den organischen Phosphaten werden vorzugsweise Alkylphosphate, Allylphosphate, Arylphosphate und insbesondere Trioctylphosphat, Kresylphosphat, Phenylphosphat, Kresylphenylphosphat und Ethylacetylhydroxybenzylphosphat eingesetzt. Verbindungen dieser ersten Gruppe werden mit Verbindungen einer zweiten Gruppe kombiniert. Diese zweite Verbindungsgruppe enthält Borsäure, Amoniumsulfonamide, anorganische Phosphate, Polyphosphate, Borate und Metallhydroxide. Besonders geeignete Borate sind Bariummetaborate, Zinkborate und Ammoniumborate, vorzugsweise verwendete Metallhydroxide sind Aluminium-und Magnesiumhydroxide. Zu den geeigneten anorganischen Phosphaten sind die Borsphosphate zu zählen, zu den Polyphosphaten die Ammoniumpolyphosphate.The above-described disadvantages of reduced flame retardancy or reduced strength are eliminated by using different combinations of flame retardants from two different connecting groups. The first linking group contains inorganic phosphate esters, phosphonated polyols, red phosphorus and organic phosphates. Of the organic phosphates, alkyl phosphates, allyl phosphates, aryl phosphates and in particular trioctyl phosphate, cresyl phosphate, phenyl phosphate, cresyl phenyl phosphate and ethyl acetyl hydroxybenzyl phosphate are preferably used. Connections from this first group are combined with connections from a second group. This second group of compounds contains boric acid, ammonium sulfonamides, inorganic phosphates, polyphosphates, borates and metal hydroxides. Particularly suitable borates are barium metaborates, zinc borates and ammonium borates; metal hydroxides which are preferably used are aluminum and magnesium hydroxides. Suitable inorganic phosphates include boron phosphates, and polyphosphates include ammonium polyphosphates.
Die verbesserte Flammwidrigkeit beruht auf einer synergistischen Wirkung des aus den beiden genannten Gruppen hergestellten Flammschutzsystems. Dadurch ist eine Erhöhung der Dosierung der Flammschutzmittel nicht notwendig. Die Menge an Flammschutzmitteln aus der ersten Gruppe liegt im Bereich von 0 - 80 Gew.-%, die Menge an Flammschutzmitteln aus der zweiten Gruppe im Bereich von 0 - 70 Gew.-%. Es reichen bereits geringe Mengen an Flammschutzmitteln aus diesen beiden Gruppen aus, um zu einer hohen Flammwidrigkeit zu gelangen. Vorzugsweise werden 10 - 40 Gew.-% an Flammschutzmitteln aus der ersten Gruppe und 20 - 60 Gew.-% an Flammschutzmitteln aus der zweiten Gruppe eingesetzt.The improved flame retardancy is based on a synergistic effect of the flame protection system produced from the two groups mentioned. It is therefore not necessary to increase the dosage of the flame retardants. The amount of flame retardants from the first group is in the range from 0 to 80% by weight, the amount of flame retardants from the second group in the range from 0 to 70% by weight. Even small amounts of flame retardants from these two groups are sufficient to achieve high flame retardancy. Preferably 10-40% by weight of flame retardants from the first group and 20-60% by weight of flame retardants from the second group are used.
Das ungesättigte Polyesterharz wird aus Terephthalsäure, Aminocarbonsäure oder ω-Aminolaurinsäure hergestellt. Zur Vernetzung wird mindestens eine Verbindung aus der Gruppe der Aryl- oder Alkyldiisocyanate, der blockierten Polyiso cyanate, der fettsäuremodifizierten Polyisocyanate oder Isophorondiisocyanat oder Triisocyanatophenyltriphosphat ausgewählt. Bevorzugte Aryl- bzw. Alkyldiisocyanate sind Tuluylisocyanat, 4,4′-Metylendi-(phenylisocyanat), Naphthalin-l,5- bzw. Naphthalin-l,4-Diisocyanat, Methylentri-(phenylisocyanat) bzw. Hexamethylendiisocyanat. Als Katalysator für die Vernetzungsreaktion kann einer oder mehrere der Verbindungen aus der Gruppe der Amine, Hydride, Metalloxide, Caroxylate, metallorganischen Verbindungen oder Tetramethylbutandiamin, Diazobicyclooctan, Dibutylzinndilaurat oder Zinnoctat ausgewählt werden.The unsaturated polyester resin is made from terephthalic acid, aminocarboxylic acid or ω-aminolauric acid. For crosslinking, at least one compound from the group of aryl or alkyl diisocyanates, the blocked polyiso cyanate, the fatty acid-modified polyisocyanate or isophorone diisocyanate or triisocyanatophenyl triphosphate selected. Preferred aryl or alkyl diisocyanates are toluyl isocyanate, 4,4'-methylene di (phenyl isocyanate), naphthalene-1, 5 or naphthalene, 1,4-diisocyanate, methylene tri (phenyl isocyanate) or hexamethylene diisocyanate. One or more of the compounds from the group of amines, hydrides, metal oxides, caroxylates, organometallic compounds or tetramethylbutane diamine, diazobicyclooctane, dibutyltin dilaurate or tin octate can be selected as the catalyst for the crosslinking reaction.
Als Stabilisatoren bzw. Alterungsschutzmittel werden vorzugsweise Verbindungen der in Ortho- oder Para-Stellung substituierten Einkern- oder Mehrkernphenole, der Bisbenzooxazole, der Cumarinderivate, Polycarbodiimide, der aromatischen Amine, Thioether, oder der Phosphite ausgewählt. Durch die Zugabe dieser Stoffe wird die unerwünschte Änderung der chemischen und physikalischen Struktur des Isolierteils während des Gebrauchs vermieden.Compounds of the mononuclear or polynuclear phenols substituted in the ortho or para position, the bisbenzooxazoles, the coumarin derivatives, polycarbodiimides, the aromatic amines, thioethers or the phosphites are preferably selected as stabilizers or anti-aging agents. The addition of these substances avoids the undesirable change in the chemical and physical structure of the insulating part during use.
Zur Färbung der verwendeten Polyesterfolie werden Farbmittel auf anorganischer oder organischer Basis verwendet. Besonders geeignete anorganische Verbindungen sind Titandioxid, Ruß, Eisenoxid, Chromoxid, Mischoxide oder Spinellverbindungen, geeignete Farbstoffe auf organischer Basis sind die Azofarbstoffe, Phtalocyanine oder Dioxazine.To color the polyester film used, colorants on an inorganic or organic basis are used. Particularly suitable inorganic compounds are titanium dioxide, carbon black, iron oxide, chromium oxide, mixed oxides or spinel compounds, suitable organic-based dyes are the azo dyes, phthalocyanines or dioxazines.
Um die elektrischen Isolierteile leichter gleitend und leichter verformbar zu machen, werden Gleitmittel zu der Beschichtung gegeben. Geeignete Verbindungen sind olefinische Ketone oder Verbindungen auf Wachs-, Seifen-oder Ölbasis.In order to make the electrical insulating parts easier to slide and easier to deform, lubricants are added to the coating. Suitable compounds are olefinic ketones or compounds based on wax, soap or oil.
Claims (16)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19873721792 DE3721792A1 (en) | 1987-07-01 | 1987-07-01 | ELECTRICAL INSULATING PARTS |
DE3721792 | 1987-07-01 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0297241A2 true EP0297241A2 (en) | 1989-01-04 |
EP0297241A3 EP0297241A3 (en) | 1990-06-20 |
Family
ID=6330713
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP88106680A Withdrawn EP0297241A3 (en) | 1987-07-01 | 1988-04-26 | Electrical insulating parts |
Country Status (2)
Country | Link |
---|---|
EP (1) | EP0297241A3 (en) |
DE (1) | DE3721792A1 (en) |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3022200A (en) * | 1960-10-12 | 1962-02-20 | Phelps Dodge Copper Prod | Magnet wire and method of making same |
US3240626A (en) * | 1962-10-23 | 1966-03-15 | Anaconda Wire & Cable Co | Electrical conductor having a first layer comprising a thermoset polyester resin and a cross-linked thermoset outer polyester resin coating |
US4257931A (en) * | 1980-01-29 | 1981-03-24 | American Cyanamid Company | Flame retardant poly(butylene terephthalate) compositions comprising melamine pyrophosphate and a phosphonate |
JPS58154771A (en) * | 1982-03-10 | 1983-09-14 | Furukawa Electric Co Ltd:The | Insulated electric wire |
EP0149171A2 (en) * | 1983-12-30 | 1985-07-24 | Ec Erdölchemie Gmbh | Flame resistant polymers |
EP0151904A1 (en) * | 1984-02-08 | 1985-08-21 | HUBER & SUHNER AG KABEL-, KAUTSCHUK-, KUNSTSTOFF-WERKE | Insulated electric cord |
JPS61151226A (en) * | 1984-12-26 | 1986-07-09 | Toshiba Corp | Lightweight electrical insulating material composition |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AT284448B (en) * | 1968-03-19 | 1970-09-10 | Beck & Co Ag Dr | Process for the production of flame-retardant, optionally foamed polyurethanes |
US3515578A (en) * | 1969-03-14 | 1970-06-02 | Minnesota Mining & Mfg | Pressure-sensitive-adhesive tape |
US4061826A (en) * | 1975-01-29 | 1977-12-06 | Minnesota Mining And Manufacturing Company | Flame-retardant pressure-sensitive adhesive composition |
US4207374A (en) * | 1978-05-05 | 1980-06-10 | Minnesota Mining And Manufacturing Company | Flame-retardant film |
-
1987
- 1987-07-01 DE DE19873721792 patent/DE3721792A1/en active Granted
-
1988
- 1988-04-26 EP EP88106680A patent/EP0297241A3/en not_active Withdrawn
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3022200A (en) * | 1960-10-12 | 1962-02-20 | Phelps Dodge Copper Prod | Magnet wire and method of making same |
US3240626A (en) * | 1962-10-23 | 1966-03-15 | Anaconda Wire & Cable Co | Electrical conductor having a first layer comprising a thermoset polyester resin and a cross-linked thermoset outer polyester resin coating |
US4257931A (en) * | 1980-01-29 | 1981-03-24 | American Cyanamid Company | Flame retardant poly(butylene terephthalate) compositions comprising melamine pyrophosphate and a phosphonate |
JPS58154771A (en) * | 1982-03-10 | 1983-09-14 | Furukawa Electric Co Ltd:The | Insulated electric wire |
EP0149171A2 (en) * | 1983-12-30 | 1985-07-24 | Ec Erdölchemie Gmbh | Flame resistant polymers |
EP0151904A1 (en) * | 1984-02-08 | 1985-08-21 | HUBER & SUHNER AG KABEL-, KAUTSCHUK-, KUNSTSTOFF-WERKE | Insulated electric cord |
JPS61151226A (en) * | 1984-12-26 | 1986-07-09 | Toshiba Corp | Lightweight electrical insulating material composition |
Non-Patent Citations (2)
Title |
---|
PATENT ABSTRACTS OF JAPAN, Band 10, Nr. 350 (C-387)[2406], 26 November 1986; & JP-A-61 151 226 (TOSCHIBA CORP.) 09-07-1986 * |
PATENT ABSTRACTS OF JAPAN, Band 7, Nr. 277 (C-199)[1422,], 9 Dezember 1983; & JP-A-58 154 771 (FURUKAWA DENKI KOGYO K.K.) 14-09-1983 * |
Also Published As
Publication number | Publication date |
---|---|
DE3721792C2 (en) | 1993-03-11 |
EP0297241A3 (en) | 1990-06-20 |
DE3721792A1 (en) | 1989-01-12 |
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