[0001] This invention relates to electrical wire and cables and to electrical conductors
suitable for use therein.
[0002] Numerous forms of electrical cable have been proposed for use in environments where
there is a risk of fire and accordingly where fire retardency of the cable is required.
These cables may make use of specific, highly effective, halogenated polymers or flame
retardant materials such as polytetrafluora- ethylene, polyvinyl chloride, or polyvinylidine
fluoride as polymers or decabromodiphenyl ether as flame retardant additives. Halogenated
systems, however, suffer from the disadvantage that when they are heated to high temperatures
during a fire, they liberate toxic and corrosive gases such as hydrogen halides, and
a number of halogen free insulating compositions have therefore been proposed, for
example in'U.S. patent specification No. 4,322,575 to Skipper and in U.K. patent specification
Nos. 1,603,205 and 2,068,347A, the disclosures of which are incorporated herein by
reference.
[0003] In certain fields where cables are used. for example in military, marine- mass transit
or offshore applications. it is desired to use cables which are capable of functioning
at relatively high temperatures. In other instances it is desired to use cables which
not only do not burn. or. if they burn. do not liberate toxic or corrosive gases.
but also are capable of functioning after having been subjected to a fire. or preferably
for a period of time during a fire without shorting or otherwise failing. Cables that
are capable of functioning for a period of time during a fire have been called circuit
integrity cables or signal integrity cables depending on their use. The previously
proposed circuit and signal integrity cables have generally used the principle that
the individual conductors should be separated from one another by mica tapes or by
large volumes of packing materials or silicones or by combinations thereof in order
to prevent the formation of short circuits during a fire. with the result that the
previously proposed cables are relatively heavy or large or both. There is therefore
a need for a cable that will function at relatively high temperatures or will function
after it has been subjected to a fire. and which preferably will retain its integrity
for a period of time during a fire but which is smaller or lighter than the previously
proposed cables.
[0004] . The present invention provides an electrical wire which comprises a copper conductor
and an electrically insulating refractory coating at least part of which has been
deposited on the conductor by a sol-gel method. the conductor including a keying layer
formed from a metal other than copper for increasing the adhesion of the refractory
coating to the conductor. According to the invention it is possible to form articles
having a refractory coating which. although being relatively thick (that is to say..in
the order of 3 to 15 micrometres) and so having good electrical insulation characteristics,
also exhibits good adhesion to the underlying metal even when subjected to mechanical
or thermal stresses.
[0005] The use of a sol-gel method for depositing the refractory coating has the advantage
that the refractory coating is substantially contaminant-free, that is to say, it
contains only those species that are intended in order for the layer to fulfill its
intended function, -and contains substantially no species that result from the manufacturing
process. An important feature of the refractory coating is good control of composition
to optimise the high temperature performance of the wire. The composition is totally
inorganic and therefore does not rely on conversion processes to occur during exposure
to normal or emergency high temperature service, as is the case for example in many
mica filled or glass filled silicone resin systems. The composition is also improved
by removing the use of polymeric binders to support inorganic materials which may
be consolidated by firing processes to form the inorganic insulation. Similarly, wires
in which the refractory coatings have been formed by electrochemical conversion of
metal layers e.g. by anodising an aluminium layer, and which do not form part of the
invention, usually have coatings that are porous and oft
.en heavily contaminated with ionic residue from the electrolytic solutions e.g. sulphates
from sulphuric acid anodisation processes.
[0006] Preferably the insulating refractory coating is formed from an electrically insulating
infusible or refractory metal or semi-metal oxide or nitride and the invention will
be described below in many cases with respect to oxides and nitrides although other
refractory coatings are included. By the term "infusible" or "refractory" is meant
that the coating material in its bulk form should not fuse or decompose when subjected
to a temperature of 800
*C, for 3 hours. Preferably the oxide or nitride should be able to withstand higher
temperatures also, for example it should be able to withstand a temperature of 1000"C
for at least 20 to 30 minutes. The preferred oxides and nitrides are those of aluminium,
titanium, tantalum and silicon or mixtures thereof with themselves or with other oxides
or nitrides. Thus, for example, the use of mixed metal oxides for the refractory coating
are also encompassed by the present invention.
[0007] The wires according to the present invention are particularly applicable for use
in systems in which they need to be capable of functioning at high temperatures for
significant lengths of time without failure, e.g. circuit and signal integrity cable
and magnet wire. The conductor may be a single, solid conductor or it may be a stranded
conductor in which individual strands are laid together to form a bundle which preferably
contains 7, 19 or 37 strands. Where the conductor is stranded it is preferred for
the bundle to be coated rather than the individual strands, that is to say, the refractory
coating extends around the circumference of the bundle but not around the individual
strands so that substantially only the outwardly lying surfaces of the outer-most
layer of strands are coated.
[0008] This form of conductor has the advantage that the inter strand electrical contact
is retained and the dimensions of the bundle are kept to a minimum.(since the thickness
of the coating may constitute a significant proportion of the strand dimensions for
fine gauge conductors) and also it aids the formation of good electrical connections,
e.g. crimp connections, to the conductor because a large proportion of the surface
of the strands. and the entire surface of the strands in the central region of the
conductor, will be uncoated by the refractory coating.
[0009] If a circuit or signal integrity cable is formed according to the invention from
a stranded conductor, it has the advantage that it is very flexible as compared with
other signal and circuit integrity cables, especially if a stranded conductor is used.
The ability of the wire to be bent around tight bends (small bend radii) without deleterious
effect is partly due to the fact that the layer providing the integrity is thinner
than with other signal and circuit integrity cables. However, when the conductor is
a stranded conductor it may be bent around tight bends without undue-stress on the
surface of the strands because the strands are displaced from a regular hexagonal
packing at the apex of the bend thereby exposing uncoated areas of the strands to
the eye. It is highly surprising that even though uncoated strands may be exposed
when the wire conductor is bent there is no electrical contact between adjacent stranded
conductors. It is believed that in this case the integrity is retained because the
profile of a stranded conductor is not cylindrical but rather is in the form of a
hexagon that rotates along the length of the conductors. so that adjacent stranded
conductors will touch one another only at a few points along their length, which points
are always provided by the outwardly oriented part of the surface of the strands in
the outer layer of the conductors. It is these points of contact that are always provided
with the refractory coating.
[0010] The refractory coating preferably has a thickness of at least 0.5, more preferably
at least 1. especially at least 2 and most especially at least 3 micrometres but preferably
not more than 15 and especially not more than 10 micrometres, the most preferred thickness
being about 5 micrometres depending upon specific operational requirements. The exact
thickness desired will depend on a number of factors including the type of layer and
the voltage rating of the wire. circuit integrity cables usually requiring a somewhat
thicker coating than signal integrity cables and sometimes above 15 micrometres. The
lower limits for the layer thickness are usually determined by the required voltage
rating of the wire whilst the upper limits are usually determined- by the time, and
therefore the cost, of the coating operation.
[0011] - As stated above, the conductor includes a keying layer formed frpm a metal other
than copper for increasing the adhesion of the refractory coating to the conductor.
The keying layer may be bonded directly to the copper or may be located on a further,
intermediate metal layer. The metal of the keying layer or the further layer is preferably
one which forms a good bond between the underlying metal and the refractory coating
and also, as described in our copending British Application entitled "Temperature
Resistant Coated Article" filed on even date herewith (Agent's Ref. RK263) (corresponding
to European Application No. 85304871.8) one which acts as a barrier to diffusion of
oxygen or copper or both or which acts to reduce stress in the refractory layer imposed
by substrate strain resulting from mechanical or thermal stress. Preferred metallic
layers include those formed from aluminium, titanium, tantalum, chromium, manganese,
silicon or nickel although other metals may be used. Examples of articles in which
they may be used are described in our copending British Patent Application entitled
"Electrical Wire & Cable" (Agent's Reference RK264) filed on even date herewith (corresponding
to European Application No. 85304872.6) the disclosures of which is also incorporated
herein by reference.
[0012] It has been found that, in such cases the metal forming the keying layer eliminates
or substantially reduces the mechanisms by which failure occurs, thus extending the
high temperature lifetime of the article. Thus, for example in the case of ciruit
or signal integrity cables the time required to cause circuit failure in a fire would
be substantially increased. The metal forming the keying layer for this purpose may
be one which acts as a barrier to diffusion of either the underlying substrate to
the outer surface of the article or to the diffusion of oxygen into the substrate.
It may restrict diffusion in its elemental form or it may hinder diffusion processes,
by formation of oxide scales when exposed to air, as is the case with for example
aluminium or nickel. Such scales are most effective if they are stable on formation
and exhibit low growth rates. The -keying layer may be formed of metals which will
alloy with the underlying substrate on exposure to high temperatures but which would
still preferentially oxidise to form stable scales on exposure' to air, or may be
formed from metallic alloys which exhibit high oxidative stability e.g. titanium/
aluminium alloys. The metal forming the keying layer may also be selected to take
advantage of physical or chemical compatibility with the substrate and refractory
layers to maximise adhesion.
[0013] In addition it has been found that in many cases the provision of a relatively thick
keying layer significantly reduces the formation of cracks in the refractory layer
when the article is subjected to mechanical abuse. It is believed that the reduction
in formation of cracks is due to the reduction of stress in the refractory layer when
the article is subjected to strain by virtue of the deformation of the intermediate
layer, and accordingly it is preferred for the keying layer to be formed from a metal
having a lower modulus than that of copper as described in the European Application
No. 85304871.8.
[0014] The metallic keying layer may be formed in a number of ways, for instance by electroplating,
standard wire cladding techniques such as roll bonding, and by vacuum deposition techniques
e.g. sputtering, evaporation, flame spraying, plasma assisted chemical vapour deposition
(CVD) or other techniques.
[0015] The refractory coating may provide the entire electrical insulation or one or more
additional insulating layers may be provided thereon. The additional insulating layer
may be inorganic or organic or a combination of inorganic and organic layers may be
provided. For example polymeric insulation may be provided in order to provide additional
insulation to the conductor during normal service conditions and also to enable the
wire to have the desired dielectric properties and other properties e.g. mechanical
properties. scuff resistance. colour coding ability etc. However, an important advantage
of the present invention is that since a significant proportion of or all the service
insulating properties are provided by the refractory coating, the electrical properties
of the polymeric insulation are not as critical as with other wire contructions in
which the polymeric insulation provides the sole insulation between the conductors.
Of the known polymeric materials that are used for electrical insulation, polyethylene
probably has the most suitable electrical properties but is highly flammable, and
has poor mechanical properties. Attempts to flame retard polyethylene have either
required halogenated flame retardants which, by their nature, liberate corrosive and
toxic hydrogen halides when subjected to fire, or have required relatively large quantities
of halogen-free flame retardants which have a deleterious effect on the electrical
properties and often also the mechanical properties of the polymer. Accordingly, an
acceptable wire has in the past only been achieved by a compromise between different
properties which is often resolved by using a relatively thick-walled polymeric insulation
and/or dual wall constructions. Although such forms of polymeric insulation may be
used with the wire according to the present invention, the presence of the refractory
layer does obviate these problems to a large extent since the polymer used for the
insulation may be chosen for its flammability and/or its mechanical properties at
the expense of its electrical properties. As examples of polymers that may be used
to form the polymeric insulation there may be mentioned polyolefins e.g. ethylene
homopolymers and copolymers with alpha olefins. halogenated polymers e.g. tetrafluoroethylene,
vinylidene fluoride. hexafluoropropylene and vinyl chloride homo or copolymers polyamides.
polyesters. polyimides. polyether ketones e.g. polyarylether ketones, aromatic polyether
imides and sulphones. silicones. alkene/vinyl acetate copolymers and the like. The
polymers may be used alone or as blends with one another and may contain fillers e.g.
silica and metal oxides e.g. treated and untreated metal oxide flame retardants such
as hydrated alumina and titania. The polymers may be used in single wall constructions
or in multiple wall constructions. for example a polyvinylidine fluoride layer may
be located on for example a polyethylene layer. The polymers may be uncrosslinked
but preferably are crosslinked, for example by chemical cross-linking agents or by
electron or gamma irradiation, in order to improve their mechanical properties and
to reduce flowing when heated. They may also contain other materials e.g. antioxidants,
stabilizers. crosslinking promotors. processing aids and the like. The polymeric insulation
may. if desired, contain a filler e.g. hydrated alumina, hydrated titania, dawsonite,
silica and the like. and especially a fil'ler that has the same chemical composition,
at least under pyrolysis conditions, as the refractory coating, so that the filler
in the polymeric insulation will provide additional insulation when the wire or cable
is subjected to a fire. A preferred type of polymeric insulation is one that will
char. for instance certain aromatic polymers mentioned above. or that will ash e.g.
a silicone polymer. when subjected to a fire so that the char or ash. together with
the refractory coating. will provide the necessary insulation during a fire. Examples
of polymers. compositions, their manufacture and wires using them are described in
U.S. Patent Specifications Nos. 3.269.862. 3,580,829, 3.953.400. 3.956.240. 4,155,823.
4.121.001 and 4,320. 224. British Patent Specifications Nos. 1.473.972, 1,603,205,
2,068,347 and 2.035.333. 1.604.405 and in European Patent Specification No. 69.598.
the disclosures of which are incorporated herein by reference. Preferably the wire
is substantially halogen free.
[0016] The polymeric insulation may be applied onto the conductor by any appropriate method.
for example by extrusion, tape winding or dip coating. In some instances, for example
when certain aromatic polymers are used, it may be appropriate to form the insulation
on the conductor by a plasma or thermal polymerisation process.
[0017] It has been found that it is possible to form articles according to the invention
that are highly resistant to high temperatures and that the integrity of the refractory
coating is not destroyed by exposure to high temperatures for relatively long periods
of time. By examination of articles in accordance with the present invention and articles
in which no metal keying layer is present, by means of a scanning electon microscope-
it has been observed that the predominant failure mechanism of articles having no
keying layer is through spalling. When articles are provided with a thin metal keying
layer the spalling is reduced and failure occurs through a mechanism in which the
underlying copper appears to migrate through the refractory layer and appear at the
outer surface of the refractory layer, in the form of small globules or a network
of "dykes" or in other cases. in the form of "blisters". This form of failure may
occur at temperatures as low as 500°C, well below the melting point of copper. The
particular reason why this failure occurs is unclear and it is likely that more than
one mechanism is responsible for the failure in different cases. One theory as to
the failure mechanism is that, at elevated temperatures. the underlying copper is
oxidized by ambient oxygen which has penetrated the refractory layer, either by diffusion
or through cracks that may have been caused by mechanical or thermal stresses in the
refractory layer. to form copper oxide (Cu
20 or Cu0) which are relatively electrically conductive. Growth of the copper oxide
scale would proceed by outward diffusion of copper through the copper oxide to combine
with inwardly diffusing oxygen until it reached the outer surface of the refractory
layer. In the case of circuit integrity wires electrical integrity of the system would
be significantly deleteriously affected.
[0018] Whatever the precise failure mechanism is, and whether the underlying copper migrates
through the refractory layer in its elemental form or in the form of its oxide, it
has been observed that this migration may be significantly reduced or prevented by
the provision of a relatively thick metal layer which acts as a barrier to diffusion
of oxygen or copper or both. For this reason, amongst others, the keying layer preferably
has a thickness of at least 0.5, more preferably at least 1, especially at least 2
and most especially at least 3 micrometres.
[0019] It has also been observed that thick intermediate layers (e.g. aluminium layers)
can act to reduce or eliminate crack formation resulting from the thermal expansion
mismatch between copper and the refractory layer, and so improve the temperature resistance
of the article.
[0020] Preferably a major part and most preferably substantially all the refractory coating
is deposited on the conductor by a sol-gel method. The sol-gel process involves the
hydrolysis and polycondensation of a metal al-koxide, for example, silicon tetraethoxide,
titanium butoxide or aluminium butoxide to produce an inorganic oxide gel which is
converted to an inorganic oxide glass by a low temperature heat treatment. The metal
alkoxides can be used as precursors to inorganic glass preparation via the sol-gel
route. The alumina gel can be prepared by adding an alkoxide of aluminium, such as
aluminium secondary butoxide, to water which is heated to a temperature above 80
*C and stirred at high speed. Approximately two litres of water per mole of alkoxide
are suitable quantities. The solution is maintained at 90°C and approximately 0.5
- 1 hour after the addition of the alkoxide a quantity of acid, for example 0.07 moles
of hydrochloric acid per mole of alkoxide, is added to peptise the sol particles.
The sol is maintained at the boiling temperature to evaporate excess butanol and reflux
conditions are established and maintained until peptisation is complete. The sols
can be reduced in volume by removal of water until a viscosity suitable for wire coating
is reached.
[0021] Wires are provided with the alumina gel for subsequent conversion to an inorganic
insulation by a dip or extrusion process. In this process the wire is drawn through
the gel prepared to a suitable viscosity, as described above. such that a controlled
thickness of gel adheres to the wire. The thickness is best controlled by wiping excess
gel from the wire using sizing dies. The gel coated wire then undergoes suitable drying
and firing stages to convert the coating into an inorganic oxide glass. The precise
conditions with respect to temperature and residence time in the various stages of
conversion are dependent upon the gel composition prepared and its tolerance to relatively
rapid changes in its environment. Porosity and integrity of the coating can be significantly
affected by these stages. A suitable conversion process would include drawing the
wire through drying ovens in which the temperature is controlled at a temperature
of approximately 80°C and subsequently through progressive heat treatment stages which
expose the wire for a few minutes to temperatures of 300°C to 500"C. The required
exposure times are dependent upon the initial thickness of the gel coating, but general
guidelines are used with the recommendation that the drying process is carried out
as slowly as practical. It may be desirable to build thickness in a multipass process
in which several thin layers are deposited sequentially.
[0022] Although wires in which the entire refractory coating has been deposited by a sol-gel
method have the advantage that they allow relatively rapid manufacturing operations.
it may be preferred in some instances to form part of the refractory coating by a
different technique. For example the underlying part of the refractory coating adjacent
to the metal keying layer may be formed by a slower deposition method such as a vacuum
deposition process in order to improve further the adhesion of the refractory coating
to the conductor. Examples of such methods include sputtering. evaporation. ion plating
and chemical vapour deposition. and are described in our copending British Patent
Applications entitled "Temperature resistant Coated Article" (Agent's reference RK263)
and
wRefractory Coated Articles" (Agent's reference RK265). filed on even date herewith,
the disclosures of which are incorporated herein by reference.
[0023] After the refractory coating has been deposited on the wire conductor it may be desirable
to coat it with a thin coating of a polymeric resin or lacquer in order to provide
mechanical protection and a barrier against water or electrolytes during service.
[0024] In order to form a circuit or signal integrity on cable the appropriate wires according
to the invention may simply be laid together and be enclosed in a jacket. If desired
the wires may be provided with a screen or electromagnetic interference shield before
the cable jacket is applied. Thus a cable may be formed in a continuous process by
means well known in the art by braiding the wire bundle and extruding a cable jacket
thereon. Any of the materials described above for the wire polymeric insulation may
be used although halogen-free compositions e.g. compositions as described in the U.K.
Patent Specifications Nos. 1.603.205 and 2.068.347A mentioned above are preferred.
[0025] It is of course possible to employ additional means for providing integrity of the
cable such as mica tape wraps. but these are not necessary nor are they desirable
in view of the increased size and weight of the cable.
[0026] The present invention is also suitable for forming flat cables which, as will be
appreciated. are not susceptible to being wrapped with mica tape. Thus it is possible
by means of the present invention to form flat cables that are capable of functioning
as circuit and signal integrity cables.
[0027] Several embodiments of the invention and a method of production thereof will now
be described by way of example with reference to the accompanying drawings in which:
Figure 1 is a cross-section through one form of wire according to the present invention-
Figure 2 is a cross-section through a signal integrity cable employing the wires of
figure 1
Figure 3 is a cross-section through part of a flat conductor flat cable- and
Figure 4 is a schematic section through part of the thickness of article in accordance
with the invention.
[0028] Referring to figure 1 of the drawings a 26
AWG stranded copper conductor formed from 19 copper strands 1 is coated with a 3 micrometre
thick keying layer of aluminium by a vacuum evaporation technique, and a refractory
aluminium oxide layer 2 having a thickness of 6 micrometres by the sol-gel method
described above. A coating 3 based on a polyetherimide sold under the trade name "ULTEM"
or a polyether ether ketone or polyether ketone is then extruded on the oxide coated
conductor to form a polymeric "insulating" layer of mean wall thickness 0.2 mm.
[0029] Figure 2 shows a signal integrity cable formed by laying together seven wires shown
in figure 1, forming an electromagnetic interference screen 4 about the bundle by
braiding and then extruding thereon a jacket 5 based on a halogen-free composition
as described in British Patr-
' Specification No. 2,068,347 Example 1A.
[0030] The cable so formed is particularly lightweight and has a relatively small overall
diameter in relation to the volume of the copper conductor.
[0031] Figure 3 shows a flat conductor flat cable comprising an array of flat copper conductors
1 with a 100 mil (2.54 mm) spacing. Each copper conductor 1 is provided with a 3 micrometre
thick aluminium keying layer and a 6 micrometre thick alumina coating thereon as described
above, and the coated conductors are embedded in a single polymeric insulating layer
formed for example from the polyether imide sold under the trade name "ULTEM" or from
a polyether ether ketone or polyether ketone.
[0032] Figure 4 is a schematic section through parts of an article according to the invention
showing a typical arrangement of layers that may be formed on the copper substrate,
the thickness of the layers being exaggerated for the sake of clarity.
[0033] A copper substrate 21 is provided with a thick (e.g. 1 to 3 micrometres) layer 22
of nickel followed by a layer 23 of aluminium metal. A layer 24 of non- stoichiometric
aluminium oxide Al
2O
x and a layer 25 of stoichiometric aluminium oxide A1
20
3 may optionally be deposited on the aluminium layer e.g. by a sputtering method. An
additional, relatively thick layer 26 of aluminium oxide (e.g. of about 5 to 15 micrometres
thickness) is deposited on the layer 25 by a sol-gel method or may be deposited directly
onto the aluminium layer 23.
[0034] The following Examples illustrate the invention.
Examples 1 to 3
[0035] In Example 1 a copper conductor was provided with a 12 micrometre thick alumina coating
by the sol-gel process described above. the coating being deposited directly onto
the copper surface.
[0036] In Example 2, a copper conductor was provided with a 3.3 micrometre thick aluminium
keying layer by means of a sputtering technique described in our copending British
Patent Application entitled "Refractory coated Article" filed op even date herewith
(Agent's reference RK265). The sputtering conditions were as follows: the wire 4 was
precleaned by vapour degreasing in 1,1,1-trichloroethane prior to deposition. The
cleaning was achieved by passing the wire through a vapour degreasing bath such that
a residence time of 3 minutes was achieved. The wire 4 was then loaded into the vacuum
chamber. The chamber was then evacuated to a pressure of 1 x 10 -6 mbar prior to starting
the process. At this stage argon was admitted to attain a pressure of 1.
5.10
-2 mbar whereupon a high frequency (80 kHz) bias potential was applied to the wire handling
system which was isolated from ground. A bias potential of -850V was achieved, and
the wire was transferred from reel 3 to reel 4 such that a residence-time of 10 minutes
was achieved. On completion of the cleaning cycle the pressure was reduced to 8.10
-3 mbar and the deposition process started.
[0037] 3 kW of DC power was applied to the aluminium target 5. The wire passed from reel
2 to reel 3 being coated as it passed the target 5. Residence time in this region
was controlled by wire speed and adjusted to give the required thickness. The roller
mechanism alternated the wire face exposed to the target as it progressed down the
target length.
[0038] The aluminium coated conductor was then provided with an alumina coating as described
with respect to Example 1.
[0039] In Example 3 a copper conductor was provided with a 3.3 micrometre aluminium keying
layer as described with respect to Example 2 and was subsequently coated with aluminium
oxide in a similar process. For this second coating, an aluminium oxide target powered
with an RF power supply was used. The wire residence time and target power were adjusted
to give a constant thickness of aluminium oxide, being about 0.2 micrometres. During
deposition of both aluminium and aluminium oxide the copper conductors were held at
a bias potential relative to the chamber to promote adhesion.
[0040] The aluminium and alumina coated conductor was then provided with a sol-gel deposited
alumina coating as described with reference to Example 1.
[0041] The samples were then tested to determine the adhesion of the top coat as follows.
A fixed length of wire was subjected to a tensile strength whilst the strain was continuously
recorded. During testing the wire sample was viewed through an optical microscope.
When the coating was seen to significantly spall the strain was recorded. The strain
value recorded at this point gave a measure of the adhesion of the coating. The composition
of the samples and the results obtained are shown in Table No. 1.

[0042] The results show a clear improvement in adhesion of the gel derived alumina coating
with the aluminium layer and a further improvement in adhesion with the vacuum deposited
aluminium oxide layer.
Examples 4 and 5
[0043] The electrical performance of wires prepared as those in Example 3, were tested by
twisting pairs of identical wires (2 twists per 2.5 cms length) to form a twisted
pair cable of 1.5 m in length. connectihg one end of the wires to a 1 MHz, 30V square
wave source and observing the wave across a 200 ohm load at the other end of the wires
by means of an oscilloscope. The twisted pair cables were subjected to heating in
a propane gas burner having a flat flame 8cm wide. The temperature of the flame just
below the twisted pairs was maintained at the required temperature and the time to
failure recorded.
[0044] In Example 4 the sample was found to survive for 70 seconds in a flame at 900"C.
In Example 5 the wires had still not failed after a flame exposure time of 72 minutes
at 650°C. The substrate material onto which the sol-gel derived aluminium oxide was
deposited for Examples 4 and 5 had a dense 0.2 micrometres coatinq of vacuum deposited
aluminium oxide on its surface. Although this layer is insulating, it was incapable
of supporting 30V at room temperature.
1. An electrical wire which comprises a copper conductor and an electrically insulating
refractory coating at least part of which has been deposited on the conductor by a
sol-gel method, the conductor including a keying layer formed from a metal other than
copper for increasing the adhesion of the refractory coating to the conductor.
2. A wire as claimed in claim 1, wherein a major part of the refractory coating, and
preferably substantially all the refractory coating, has been deposited on the conductor
by a sol-gel method.
3. A wire as claimed in claim 1 or claim 2, wherein the refractory coating has a thickness
greater than 1 micrometre preferably greater than 2 micrometres.
4. A wire as claimed in any one of claims 1 to 3, wherein the refractory coating comprises
a number of layers that have been deposited by a sol-gel method.
5. A wire as claimed in any one of claims 1 to 4, wherein the refractory coating comprises
a metal oxide.
6. A wire as claimed in any one of claims 1 to 5, wherein the refractory coating comprises
a compound of silicon, aluminium or titanium or tantalum.
7. A wire as claimed in any one of claims 1 to 6, wherein the keying layer comprises
nickel, aluminium, titanium, manganese, tantalum, chromium, or an alloy thereof.
8. A wire as claimed in any one of claims 1 to 7, wherein the keying layer comprises
the same metal as that present in the refractory layer.
9. A wi.re as claimed in any one of claims 1 to 8, wherein the keying layer has a
thickness of at least 0.5, preferably at least 1, more preferably at least 2, and
especially at least 5 micrometres.
10. A wire as claimed in any one of claims 1 to 9, wherein the keying layer has been
formed by a vacuum deposition technique, preferably by a metal rolling method, an
electroplating method or by drawing the wire through a metal melt.
11. A wire as claimed in any one of claims 1 to 10, wherein the metal from which the
keying layer is formed has a higher ductility than that of copper.
12. A wire as claimed in any one of claims 1 to 11, wherein the keying layer is formed
.from a metal that acts as a barrier to diffusion of copper or oxygen or both.
13. A wire as claimed in any one of claims 1 to 12, which has one or more additional
layers on top of the refractory coating or between the refractory coating and the
keying layer.
14. A wire as claimed in any one of claims 1 to 13, wherein the conductor is a stranded
conductor and the refractory coating extends around the conductor but not around the
individual strands thereof.
15. A wire as claimed in any one of claims 1 to 14, which is provided with an additional
layer of polymeric insulation.