DE2441106A1 - COPPER CONDUCTOR - Google Patents
COPPER CONDUCTORInfo
- Publication number
- DE2441106A1 DE2441106A1 DE19742441106 DE2441106A DE2441106A1 DE 2441106 A1 DE2441106 A1 DE 2441106A1 DE 19742441106 DE19742441106 DE 19742441106 DE 2441106 A DE2441106 A DE 2441106A DE 2441106 A1 DE2441106 A1 DE 2441106A1
- Authority
- DE
- Germany
- Prior art keywords
- polyethylene
- alkyl
- antioxidant
- radicals
- copper
- 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- Withdrawn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
- 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
- H01B3/308—Wires with resins
-
- 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
- H01B3/44—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 vinyl resins; acrylic resins
- H01B3/441—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 vinyl resins; acrylic resins from alkenes
Description
Dipl.-Ing. Tiedtke
Dipl.-Chem. Bühling Dipl.-Ing. KinneDipl.-Ing. Tiedtke
Dipl.-Chem. Bühling Dipl.-Ing. Chins
8 München 28 Munich 2
Tel.:(089)539653-56 Telex: 524845 tipat cable address: Germaniapatent MünchenTel.:(089)539653-56 Telex: 524845 tipat cable address: Germaniapatent Munich
München, den 28. August 1974 B 6174 / ICI case Po.26415Munich, August 28, 1974 B 6174 / ICI case Po.26415
Imperial Chemical Industries Limited
London, GroßbritannienImperial Chemical Industries Limited
London, UK
Kupferleiter.Copper conductor.
Die Erfindung bezieht sich auf Kupferleiter in Kontakt mit einer Polyäthylenmasse.The invention relates to copper conductors in contact with a polyethylene compound.
Seit der Entdeckung von Polyäthylen wurde dieses zur Isolierung von Kupferleitern in Telefonkabeln und Radar-Since the discovery of polyethylene, it has been used to insulate copper conductors in telephone cables and radar
installationen verwendet. Das als Isolierung normalerweise verwendete Polyäthylen enthält kleine Mengen an einer antioxydierenden Verbindung, welche die Zersetzungseffekte von Sauerstoff auf das Polyäthylen verringert, und Polyäthylenisolierung, welche sich in Kontakt mit Kupfer befindet, enthält häufig einen sog. Kupferstabilisator, wie N,N1-Diacetylinstallations used. The polyethylene normally used as insulation contains small amounts of an antioxidant compound which reduces the decomposition effects of oxygen on the polyethylene, and polyethylene insulation which is in contact with copper often contains a so-called copper stabilizer , such as N, N 1 -diacetyl
509810/0855509810/0855
ι) Kto. 51/61070 Dresdner Bank (München) Kto. 3339844 Postscheck (München) Kto. 67043-804 ι) Account 51/61070 Dresdner Bank (Munich) Account 3339844 Postscheck (Munich) Account 67043-804
II/8II / 8
Deutsche Bank (MünchenDeutsche Bank (Munich
2U11062U1106
(adipoyldihydrazid) oder Nickel-bis-(3,5-ditert.butyl-4-hydroxybenzylphosphonsäuremonoäthylat), welcher Sprödig-, keit vermindert,, die in Gegenwart von Kupfer auftritt. Diese.sog. Kupferstabilisatoren sind im allgemeinen teure Materialien.(adipoyldihydrazide) or nickel-bis- (3,5-di-tert-butyl-4-hydroxybenzylphosphonic acid monoethylate), which reduces brittleness, which occurs in the presence of copper. This. Suction. Copper stabilizers are generally expensive materials.
Antioxidantien, wie 2,2'-Methylen-bis^6- (ot-methylcyclohexyl)-4-methylphenol7 und ähnliche Verbindungen, beschrieben in der britischen Patentschrift 744 875, sind seit über 15 Jahren im Handel erhältlich und sind in nichtbestrahlter Polyäthylenisolierung in Mengen von bis zu 0,1 % verwendet worden, obwohl Mengen in einer Größenordnung von 1 Gew.-% der Antioxidantien zur Verwendung in thermoplastischen Kautschuken vorgeschlagen worden sind, wo der Verlust an Antioxidanz durch "Ausblühen" (d.h. Ausschwitzen des Antioxidanz aus dem Thermoplasten) von geringerer Bedeutung ist und wo angenommen wird, daß die Antioxidantien ebenfalls das Einsetzen von Kupfer-katalysierter Oxydation des Kautschuks verzögern.Antioxidants such as 2,2'-methylene-bis ^ 6- (ot-methylcyclohexyl) -4-methylphenol7 and similar compounds described in British Patent 744,875 available in stores for over 15 years and in non-irradiated polyethylene insulation in quantities of up to 0.1% has been used, although amounts on the order of 1% by weight of the antioxidants for use in thermoplastic Rubbers have been suggested where the loss of antioxidant by "blooming" (i.e. exudation of the Antioxidant from the thermoplastic) is of less importance and where it is assumed that the antioxidants also delay the onset of copper-catalyzed oxidation of rubber.
Es wurde nun gefunden, daß die Anwesenheit bestimmter spezifizierter Mengen an 2,2'-Methylen-bis^6-(OL-methylcyclohexyl)-4-methylphenol7 und ähnlicher Antioxidantien in Polyäthylen, welches sich in Kontakt mit Kupfer befindet, nicht zu übermäßigem Ausblühen führt und Sprödigkeit des Polyäthylens durch das Kupfer reduziert, i.It has now been found that the presence of certain specified amounts of 2,2'-methylene-bis ^ 6- (OL-methylcyclohexyl) -4-methylphenol7 and similar antioxidants in polyethylene, which is in contact with copper, does not lead to excessive blooming and reduces the brittleness of the polyethylene by the copper, i.
509810/0855509810/0855
Demgemäß ist Gegenstand der Erfindung ein Kupferleiter in Kontakt mit einer Polyäthylenmasse, dadurch gekennzeichnet, daß die Polyäthylenmasse zwischen 0,2 bis 0,8 Gew.-% eines Antioxidanz enthält, nämlich Dihydrpxypheriol oder ein normales oder basisches Aluminium-, Barium-, Calcium-, Magnesium-, Strontium- oder Zinksalz hiervon, wobei das Dihydroxyphenol die allgemeine FormelAccordingly, the invention provides a copper conductor in contact with a polyethylene mass thereby characterized in that the polyethylene composition contains between 0.2 to 0.8 wt .-% of an antioxidant, namely Dihydrpxypheriol or a normal or basic aluminum, barium, calcium, magnesium, strontium or zinc salt thereof, where the dihydroxyphenol has the general formula
OHOH
besitzt, worin R1 und R. Alkylreste, vorzugsweise primäre Alkylreste mit 1 bis 3 Kohlenstoffatomen sind, R, und R. Alkyl-, Cycloalkyl- oder Alkyl-substituierte Cycloalkylreste bedeuten und R^ ein Alkylenrest ist, welcher Seitenketten-Alkylgruppen enthalten kann. Die Reste R- und R. können gleich oder verschieden sein, sind jedoch vorzugsweise beide Methylgruppen. Die Reste R_ und R3 können ebenfalls gleich oder verschieden sein. R kann beispieleweise ein Methylen-, Äthylen-, Isopropylen- oder 4-Methylpentylenrest sein. Ein bevorzugtes Antioxidanz ist 2#2' -Methylen-bia^i)-(α,-methylcyclohexyl) -4-methylρhenol7.in which R 1 and R. are alkyl radicals, preferably primary alkyl radicals having 1 to 3 carbon atoms, R and R. are alkyl, cycloalkyl or alkyl-substituted cycloalkyl radicals and R ^ is an alkylene radical which can contain side chain alkyl groups. The radicals R- and R. can be identical or different, but are preferably both methyl groups. The radicals R_ and R 3 can also be identical or different. R can be, for example, a methylene, ethylene, isopropylene or 4-methylpentylene radical. A preferred antioxidant is 2 # 2 '-methylene-bia ^ i) - (α, -methylcyclohexyl) -4-methylρhenol7.
Bevorzugt enthält die Polyäthylenmasse 0,3 bis 0,5 Gew.-% Antioxidanz.The polyethylene composition preferably contains 0.3 to 0.5% by weight of antioxidant.
509810/0855509810/0855
2U11062U1106
Es ist besonders bevorzugt, daß die Polyiithylenmasse geschäumt ist. Die Polyäthylenmasse kann mittels Blähmitteln, wie Azodicarbonamid oder Diphenyloxyd-4,4'-disulphohydrazid geschäumt sein. Andere Blähmittel sind in einem Artikel von Dr. A.H. Scheurlen in "Kunststoffe", Band 47, Nr. 8 (1957),. Seiten 446 bis 455, beschrieben.It is particularly preferred that the polythene composition is foamed. The polyethylene mass can by means of blowing agents such as azodicarbonamide or diphenyloxyd-4,4'-disulphohydrazide be foamed. Other blowing agents are discussed in an article by Dr. AH. Scheurlen in "Kunststoffe", Volume 47, No. 8 (1957) ,. Pages 446 to 455.
Die Erfindung wird durch folgendes Beispiel näher erläutert.The invention is explained in more detail by the following example.
Eine Polyäthylenmasse mit einem Schmelzfluß-Index von 0,3 (gemessen nach British Standard 2782, Teil 1/105C/ 1970 unter Verwendung einer 2,16 kg-Belastung) und einerA polyethylene mass with a melt flow index of 0.3 (measured according to British Standard 2782, part 1 / 105C / 1970 using a 2.16 kg load) and one
2
Dichte von 0,932 kg/cm (gemessen nach British Standard 3412, 1966) und mit einem Gehalt von 0,3 Gew.-% 2,2'-Methylenbis^G(Ct-methylcyclohexyl)-4-methylphenol/
und 0,6 Gew.-% Azodicarbonamid wurde auf Kupferdraht durch Extrusion aufgetragen,
um so eine geschäumte Polyäthylenschicht zu erzeugen, die 0,1 mm dick war. Proben des beschichteten Leiters
wurden dann in einen Ofen gehängt, der bei 1O5°C 1000 Stunden gehalten wurde. Die Proben wurden dann entfernt, und es wurde
gefunden, daß sie alle über 360° ohne Rißbildung gebogen werden konnten. Hieraus konnte geschlossen werden, daß keine
ernsthafte Versprödung des Polyäthylens stattgefunden hatte.2
Density of 0.932 kg / cm (measured according to British Standard 3412, 1966) and with a content of 0.3% by weight of 2,2'-methylene bis ^ G (Ct-methylcyclohexyl) -4-methylphenol / and 0.6% by weight .-% azodicarbonamide was applied to copper wire by extrusion so as to produce a foamed polyethylene layer which was 0.1 mm thick. Samples of the coated conductor were then hung in an oven held at 105 ° C. for 1000 hours. The samples were then removed and found that they could all be flexed through 360 ° without cracking. From this it could be concluded that no serious embrittlement of the polyethylene had taken place.
509810/085b509810 / 085b
Claims (2)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB4088473A GB1472858A (en) | 1973-08-30 | 1973-08-30 | Coper conductors in contact with a polyethylene composition |
Publications (1)
Publication Number | Publication Date |
---|---|
DE2441106A1 true DE2441106A1 (en) | 1975-03-06 |
Family
ID=10417104
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19742441106 Withdrawn DE2441106A1 (en) | 1973-08-30 | 1974-08-28 | COPPER CONDUCTOR |
Country Status (8)
Country | Link |
---|---|
JP (1) | JPS5072943A (en) |
BE (1) | BE819302A (en) |
CA (1) | CA1045917A (en) |
DE (1) | DE2441106A1 (en) |
FR (1) | FR2242755A1 (en) |
GB (1) | GB1472858A (en) |
IT (1) | IT1020115B (en) |
NL (1) | NL7411199A (en) |
-
1973
- 1973-08-30 GB GB4088473A patent/GB1472858A/en not_active Expired
-
1974
- 1974-08-22 NL NL7411199A patent/NL7411199A/en not_active Application Discontinuation
- 1974-08-22 IT IT2651374A patent/IT1020115B/en active
- 1974-08-26 FR FR7429097A patent/FR2242755A1/fr not_active Withdrawn
- 1974-08-28 BE BE147996A patent/BE819302A/en unknown
- 1974-08-28 CA CA208,012A patent/CA1045917A/en not_active Expired
- 1974-08-28 DE DE19742441106 patent/DE2441106A1/en not_active Withdrawn
- 1974-08-30 JP JP9906974A patent/JPS5072943A/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
AU7253874A (en) | 1976-02-26 |
NL7411199A (en) | 1975-03-04 |
BE819302A (en) | 1975-02-28 |
CA1045917A (en) | 1979-01-09 |
FR2242755A1 (en) | 1975-03-28 |
JPS5072943A (en) | 1975-06-16 |
IT1020115B (en) | 1977-12-20 |
GB1472858A (en) | 1977-05-11 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
8139 | Disposal/non-payment of the annual fee |