GB1564990A - Creation of Inventions and Patents with Artificial Intelligence

GB1564990A – Electrical insulation compositions
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GB1564990A – Electrical insulation compositions
– Google Patents
Electrical insulation compositions

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Publication number
GB1564990A

GB1564990A
GB31443/77A
GB3144377A
GB1564990A
GB 1564990 A
GB1564990 A
GB 1564990A
GB 31443/77 A
GB31443/77 A
GB 31443/77A
GB 3144377 A
GB3144377 A
GB 3144377A
GB 1564990 A
GB1564990 A
GB 1564990A
Authority
GB
United Kingdom
Prior art keywords
polyethylene
alcohol
insulation
electrical
tree
Prior art date
1976-07-28
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.)

Expired

Application number
GB31443/77A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

EIDP Inc

Original Assignee
EI Du Pont de Nemours and Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
1976-07-28
Filing date
1977-07-26
Publication date
1980-04-16

1977-07-26
Application filed by EI Du Pont de Nemours and Co
filed
Critical
EI Du Pont de Nemours and Co

1980-04-16
Publication of GB1564990A
publication
Critical
patent/GB1564990A/en

Status
Expired
legal-status
Critical
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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

H01B3/44—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

C—CHEMISTRY; METALLURGY

C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON

C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients

C08K5/00—Use of organic ingredients

C08K5/04—Oxygen-containing compounds

C08K5/05—Alcohols; Metal alcoholates

Description

(54) “ELECTRICAL INSULATION COMPOSITIONS”
We, E.I. DU PONT DE NEMOURS AND
Co, a Corporation organised and existing under the laws of the State of Delaware, United
States of America of Wilmington, State of
Delaware, United States of America, do hereby declare the invention, for which we pray that a patent may be granted to us, and the method by which it is to be performed, to be particularly described in and by the following statement:
This invention relates to electrical insulation such as primary insulation which is particularly suitable for use in high voltage cable and to a composition of polyethylene which incorporates an additive providing resistance to electrical breakdown of the cable.
More specifically, this invention relates to improving the resistance to electrical failure of low density polyethylene and crosslinked low density polyethylene.
Electrical failure of high voltage insulation is often initiated at contaminating particles.
It is extremely difficult, if not impossible, to extrude solid organic insulation, such as polyethylene, on a conductor without any flaws.
Even if the polyethylene manufacturer uses extremely clean techniques, contaminants can later be introduced in subsequent handling of the resin prior to final shaping. Another cause of electrical failure in the insulation is the presence of a void.
High voltage power cables insulated with insulating polymers are subject to dielectric breakdown by a mechanism known to the trade as electrical “treeing”. Treeing is a re latively slow progressive degradation of an insulation caused by electron and ion bombardment of the insulation resulting in the formation of microchannels or tubes having a treelike appearance, hence the name, A tree initiates at points of contamination or voids which are foreign to the polymeric insulation by the action of ionization (corona) during high voltage surges. Once a tree starts it usually grow, particularly during further high voltage surges, and at some undetermined time, dielectric failure can occur.
To overcome this problem, various additives have been disclosed, particularly in polyethylene or other polyolefin, which require an increase in applied voltage to cause initiation of a tree.
This use of an additive attempts to prevent failure of the insulation by preventing any formation of trees.
Maloney U.S. Patent 3,449,791 discloses a coating for an electrical high voltage cable comprising a polyethylene resin which contains an inorganic ionic salt of a strong acid and a strong Zwitter-ion compound. An insulated cable provides resistance to electrical breakdown and stress cracking under the influence of corona.
Kato et al., U.S. Patent 3,956,420 discloses insulation with improved electrical breakdown resistance comprising polyolefin, a ferrocene compound and a substituted quinoline compound. Also disclosed in the patent is additional use of a small amount of polyhydric alcohol, dispersant, surfactant or unsaturated polymer or mixture thereof to obtain another improvement in electrical breakdown strength.
MacKenzie, Jr. U.S. Patent 3,795,646 discloses an ethylene-containing polymer composition which exhibits improved ionization resistance under high voltage stress by employing a silicone fluid in a crosslinked polyethylene composition.
Japanese Patent No. 14348/75 relates to wire cables with improved dielectric breakdown resistance provided by an insulation of polyethylene containing 0.1So by weight of an aromatic ketone.
German Patent 2147684 discloses the concept of increasing the electrical breakdown resistance of polymers, especially polyethylene, by modifying the free path of charge carriers (electrons) by incorporating additional scatter centers or by reducing the crystallinity of the polymer.
Japanese Patent Publication 7201988 discloses insulated power cable having improved breakdown resistance by providing an insulated layer of polyethylene, polypropylene, polycarbamate of polyester containing mica particles coated with hydrophobic insulating material of silicone oil, stearic acid, palmitic acid, or oleic acid.
Japanese Laid-Open Specification 49/119,937 discloses electric insulating resin compositions which give an increase in dielectric breakdown voltage through mixing into a resin composition such as polyethylene a ferrocene-aldehyde (or ketone) polymer having ferrocene groups or a mixture of the ferrocene containing polymer and a higher polyhydric alcohol.
This invention is directed to a composition suitable for use as electrical insulation which consists essentially of low density polyethylene or crosslinked low density polyethylene and an effective amount of at least one monohydric alcohol of 6 to 24 carbon atoms which is a tree growth inhibitor capable of providing at least a thousand-fold increase in electrical endurance of polyethylene as measured by an electrical endurance test procedure set out herein.
The composition of the invention can contain the polyethylene and optionally a peroxide cross-linking agent or can contain the crosslinked polyethylene which has been cross-linked, for example, by a peroxide cross-linking agent.
The invention also provides an article comprising an electrical conductor and an insulating layer of the composition of the invention. In such an article a semi-conducting layer can be provided between the electrical conductor and the insulating layer.
The accelerated test procedure referred to as
Test Method A herein shows the presence of the alcohol inhibits electrical tree growth (but not tree formation) and results in at least a thousandfold increase in electrical endurance of the polyethylene or cross-linked polyethylene. Such test is believed to provide a direct correlation with long term electrical endurance of such insulation on a conductor, i.e. an increased useful life of insulation when employed in its intended use.
As employed in the present specification the term “polyethylene” or “cross linked polyethylene” is limited to a homopolymer or copolymer containing no less than 85 weight percent ethylene polymerized units and no less than 95 weight percent of olefin polymerized units. These polymers would conform to the definition of “polyethylene plastics” defined in 1976 Annual Book of ASTM
Standards, 1976, Part 36, page 70 as “plastics or resins prepared by the polymerization of no less than 85% ethylene and no less than 95 weight percent of total olefins”. A preferred polyethylene or a crosslinked polyethylene contains about 100 weight percent polymerized units.
Suitable olefins which can be employed as comonomers include propylene, butene-l, hexene-l, octene-l and decene-l. Other comonomers include norbornene, butadiene, styrene, methacrylic acid, vinyl acetate, ethyl acrylate, isobutyl acrylate, and methyl vinyl ether.
The term “polyethylene” is limited to a polymer which is substantially free of crosslinks while the term “crosslinked polyethylene” defines a polymer containing crosslinks. These crosslinks can be formed by an mechanism such as by use of irradiation or a peroxide crosslinking agent.
Low density polyethylene or crosslinked low density polyethylene is suitable for use in the present invention. The higher density polyethylenes are not suitable for use in the present invention because there is little or no improvement, certainly no thousand-fold improvement, in the electrical endurance thereof upon addition of an alcohol as specified herein.
“Low density” refers to a polyethylene or crosslinked polyethylene which has a density up to 0.92 g/cc. Reference is also made to
ASTM D 1248-74 for the term “low density”.
Additionally, rigidity of an insulation is a factor in selection of a polyethylene for some uses, e.g. flexibility is necessary in transmission line cable.
The necessary additive to polyethylene or crosslinked polyethylene in the present invention is a monohydric alcohol of 6 to 24 carbon atoms and most preferably 8 to 12 carbon atoms. Preferred alcohols are aliphatic. The alcohols can be either straight or branched chain,
Suitable examples include n-hexyl, n-heptyl, n-octyl, n-decyl, n-dodecyl, n-tetradecyl, stearyl, and eicosyl alcohols, benzyl alcohol, 2-decanol, Qdecanol, cyclohexanol, 3-methylheptanol-3, 2-methyloctanol-2 and 2-phenylpropanol-2. The alcohols useful herein are also referred to in this specification as “tree growth inhibitors”.
The alcohol can be added by any conventional method, including mixing with the solid polyethylene prior to compounding or extrusion, injection into molten polyethylene, diffusion into solid polyethylene or crosslinked polyethylene of alcohol applied by spraying, soaking or vapor contacting, and contacting an article comprising polyethylene or crosslinked polyethylene with liquid or vapor-phase alcohol.
A test method, Test Method A, for determining whether an additive is suitable to increase electrical endurance at least a thousandfold employs polyethylene and excludes a peroxide crosslinking agent and crosslinked polyethylene. Since conversion of polyethylene of crosslinked polyethylene through use of a peroxide crosslinking agent can result in increase in electrical endurance, the addition of a peroxide crosslinking agent can mask to some degree the improvement imparted by a tree growth inhibitor. However, modification of
Test Method A to employ crosslinked polyethylene rather than polyethylene has proven satisfactory as a screening technique to demonstrate whether some improvement exists in accelerated electrical endurance through addition of an additive.Such modification of Test
Method A is not sufficient to determine if at least a thousand-fold improvement in electrical endurance exists in all instances.
In Test Method A initiation of a tree is necessary in a sample of insulation. Crosslinked polyethylene allows visual inspection of a tree.
In contrast, polyethylene is opaque and does not permit visual determination of a tree without cutting into the polyethylene. Therefore, in
Test Method A using polyethylene, it is generally necessary to employ several samples and destroy one of the samples to determine if a tree has been grown under initial voltage conditions.
While Test Method A excludes the presence of a peroxide crosslinking agent to determine if an additive imparts at least a thousand-fold increase in accelerated electrical endurance to low density polyethylene, the scope of the present invention includes a composition of matter consisting essentially of polyethylene or crosslinked polyethylene (crosslinked by any mechanism including use of a peroxide) and an alcohol and use of such composition thereof with an electrical conductor.
A concentration of alcohol necessary to impart at least a thousand-fold increase in time to failure as measured by Test Method A is referred to as “an effective amount”. This concentration (based on weight of alcohol to weight of polyethylene) directly results in at least the thousand-fold increase in life in low density polyethylene which is not crosslinked.
It is understood for crosslinked low density polyethylene that an effective amount of an alcohol is taken to be the same concentration of alcohol which would be necessary to bring at least a thousand-fold increase in low density polyethylene. Generally, a monohydric alcohol will be present in a weight of 0.5 to 10% of weight of the polyethylene or crosslinked polyethylene and more preferably 1% to 5% by weight.
Larger concentrations of alcohol can be beneficially employed. However, such additive can increase the power factor of the polyethylene or crosslinked polyethylene and an excess should not be employed where a higher power factor is detrimental, e.g. in high voltage transmission lines. Preferably in such use, the insulating composition will have a power factor not greater than 1%, preferably not greater than 0.5%.
A most preferred composition in the present invention contains polyethylene, a peroxide crosslinking agent and a tree growth inhibitor of at least one monohydric alcohol of 8 to 12 carbon atoms. This most preferred composition is a precursor to an insulation containing crosslinked polyethylene and its use with an electrical conductor.
Conventional peroxide crosslinking agents well known in the prior art for crosslinking polyethylene can be employed herein and include di-alpha-cumyl peroxide, 2,5-bis (t-butyl peroxy-2, 5-dimethyl hexane and 2,5-dimethyl-2, 5-di (ti-butyl peroxy) hexyne-3.
If a peroxide crosslinking agent is soluble in the alcohol, this agent can be dissolved in such alcohol and both added to polyethylene.
The polyethylene containing these additives normally is not crosslinked until after application to an electrical conductor.
For purposes of explanation and without being bound to any theory concerning the manner in which a monohydric alcohol functions for tree growth inhibition, such alcohol has the ability to diffuse through polyethylene or crosslinked polyethylene and into voids in the insulation. Tree growth in the insulation follows initial formation of microchannels and produces a tree-like appearance. Tree growth will ordinarily continue until dielectric failure of the insulation occurs. In the present case, however, it is believed that a monohydric alcohol as defined in the present invention diffuses into the voids and impedes the electron and ion bombardment. Inhibition of tree growth after initiation translates to an increase in electrical endurance of the insulation.
The underlying purpose in the test procedure is to mimic a mechanism which causes dielectric failure. In practice, trees generally initiate in power cables during high voltage surges, e.g. due to switching transients or lighting bolts, Thereafter failure of the insulation can occur at normal operating stress or particularly during additional high voltage surges. In the composition of this invention an alcohol functioning for tree growth inhibition extends useful life of the insulation by inhibiting growth of trees after their initiation and preventing premature failure of the insulation.
Unlike conventional test procedures in the prior art which determine dielectric strength of an insulation, Test Method A is considered to give a correlation to useful life of the insulation. In this latter test, a high AC voltage initially applied across electrodes within the insulation causes tree initiation without resulting in failure of the insulation. This tree initiation is followed by a rest period in which a voltage is not imposed for at least 24 hours.
Thereafter, time to failure of the insulation is measured with 12,000 volts impressed between electrodes separated by 2 mm, i.e. with an average electrical stress, if the field were uni form, of 6,000 volts/mm (as described in Test
Method A). The field, however, is intensified as a result of the small diameters of the shaped ends of the electrodes to a value greater than 6,000 volts/mm.
The accelerated electrical endurance test is believed to provide a useful correlation to the extended life of insulation which is employed for prolonged time periods, e.g. at least 30 years. It is, of course, impractical to run such long term testing, Also, only a relatively few samples will actually fail in long term testing and a statistical study would be necessary. With the presence of the monohydric alcohol in a composition consisting essentially of polyethylene, it is believed that in normal use no failure based on dielectric breakdown of polyethylene will occur.
The test for determining an increase in electrical endurance is referred to as Test
Method A and comprises the following:
Test Method A
Polyethylene for testing in accordance with this method is initiallv molded into a block termed herein as a “SPING” (which is an acronym for solid phase internal needle gap specimen). A SPING is 25 mm square by 6 mm thick and contains two electrodes embedded therein lengthwise and in line, equidistant from the faces and from the opposite edges, with the tips spaced 2 mm apart at the center of the block. Each electrode is about 30 mm in length and about 0.6 mm in diameter. One electrode has a cone-shaped point at a 300 included angle with a radius of 5 um and is the high voltage electrode; a second electrode has a 0.3 mm radius hemisphere ground on one end and is the gruund electrode.
A minimum of five SPINGS are placed on test at one time. Each SPING is placed under silicone oil which prevents surface flashover. The high voltage electrode is connected to a high voltage bus while the ground electrode is connected to a spaced pair of 6.25 centimeter spheres connected to ground through a 1 megohm resistor. A gap is set sufficiently wide between the spheres to achieve a voltage sufficient to initiate a tree in the SPING. For example, with the spheres set at 0.762 centimeter gap, a voltage (60 Hz) increasing at a rate of 500 volts/ sec is applied until a discharge occurs between the two spheres.Before this breakdown occurs, the stress on the specimen is essentially zero; however, the instant the air gap breaks down, the applied voltage plus a radio frequency signal developed by the arc is impressed across the specimen electrodes and is maintained for 1 to 2 seconds, so that a tree is generated. The voltage
required to initiate a tree will vary with the composition being tested. For polyethylene which contains an alcohol in accordance with the present invention, a voltage of 35 to 40 kV.
is required. For polyethylene which contains
other additives, the voltage required may be higher or lower, but the voltage to be used is easily determined by visual examination of each specimen to see whether a tree has been initiated.
After the tree has been initiated, the SPING is held without application of voltage for about 24 hours before placing on high voltage of
12,000 volts applied between the electrodes (an average applied voltage of 6000 v/mm). The time in hours necessary for the middle sample to fail (e.g. third out of five, fifth out of nine, in terms of time to failure) is measured and
called electrical endurance.
Failure is indicated by dielectric breakdown.
When failure occurs, a tree gaps the two electrodes resulting in a sudden increase in current (which can be indicated on a recording
ammeter) and terminates the test on that speci
men.
The tree growth inhibitor in the present invention functions in a different manner from prior art additives to obtain an improved result.
The prior art additives are generally disclosed as compounds which, when incorporated into polyethylene or other suitable insulating materials, will require a higher characteristic voltage to initiate a tree at a needle tip. (These teachings generally employ a sharp needlepoint embedded in the sample. The manner varies in which a second electrode is present). The characteristic voltage is that voltage wherein one-half of the samples on test will initiate a tree in one hour. This is determined by examining several groups of specimens at several different voltages. The test is concluded when the characteristic voltage is found.
In contrast, in the present invention, a tree growth inhibitor is not for the purposes of preventing tree initiation but solely for the purpose of suppressing growth of a tree after it has been initiated.
Although the present invention includes a composition of polyethylene or crosslinked polyethylene and a monohydric alcohol, it is understood that other conventional additives can be and are normally present in the composition. These additives include antioxidants, e.g. polymerized trimethyl-dihydroquinone; lubricants, e.g. calcium stearate; pigments, e.g. titanium dioxide; fillers, e.g. glass particles; and reinforcing agents, e.g. fibrous materials such as asbestos and glass fibers.
Although an insulation of polyethylene or crosslinked polyethylene containing a tree-growth inhibitor is particularly suitable for power cable for carrying voltage at least 15 kV, such as 15 to 220 kV, it is likewise suitable for lower or higher voltage applications. In electrical cable, in conformance to prior art teachings, a semiconducting layer would be interspaced between an electrical conductor and an insulating layer.
Such semiconducting layer conventionally includes an insulating composition which also contains carbon black.
To illustrate the present invention, the following examples are provided.
Identification of Insulation
Composition for Control A
and Examples 1-4.
(A) Polyethylene: Homopolymer
Melt Index (ASTM D-1238) 1.8 grams per
10 minutes
Density 0.918 gram per cubic centimeter
(measured in accordance with ASTM D1505-68 (Reapproved 1975 (B) Antioxidant: 4,4′ -thiobis (6-tert-butyl
m-cresol) 1500 ppm (C) Tree Growth Inhibitor: n-dodecyl
alcohol, except for Control A
Control A (No Tree Growth Inhibitor)
Test Method A
Order of Time of Failure,
SPING No. Failure Hours
1 1 0.10
2 2 0.25
3 5 0.38
4 4 0.35
5 3 0.25
Examples 1 and 2
In Example, 1 n-dodecyl alcohol was added to polyethylene pellets by tumble blending followed by extrusion mixing. In Example 2, the n-dodecyl alcohol was injected using a gear pump into molten polyethylene in the mixing zone of the extruder.In each of
Examples 1 and 2, the final concentration of the n-dodecyl alcohol was 3% by weight in the polyethylene as measured by infrared spectrometry. Nine SPINGS were prepared for each Example and placed on test using
Test Method A.
The nine SPINGS for Examples 1 and 2 were taken off test without any having failed after 1960 hours and 1730 hours respectively.
Electrical endurance would thus be in excess of 1960 hours and 1730 hours, respectively.
Continued testing of the same SPINGS was carried out. The nine SPINGS for Examples 1 and 2 were later taken off test without any having failed after a total of 4000 hours. In each case, electrical endurance would thus be in excess of 4000 hours.
Comparison of Examples 1 and 2 with Control A shows that increase of electrical endurance would be well in excess of a thousand-fold.
Examples 3 and 4
In these examples, the additive was also ndodecyl alcohol in a concentration of about 3 weight percent in the polyethylene as measured by infrared spectrometry. In Example 3, the polyethylene was mixed with the alcohol in a Banbury mixer while in Example 4 the mixing was done in a Brabender mixer. Nine SPINGS were prepared from the composition of each
Example and were placed on test by Test
Method A. All SPINGS of Example 3 were removed from test after 850 hours while in
Example 4 all SPINGS were removed from test after 720 hours. No SPINGS had failed in either Example 3 or 4. The electrical endurance was thus greater than 850 and 720 hours, respectively. The increase in electrical endurance compared with Control A is in excess of a thousand-fold.
In the remaining examples, (Examples 5 to
10) and in Controls B to D, Test Method A was still used, but with the minor changes that each electrode was 1.0 mm in diameter (instead of 0.6 mm), and the second electrode was ground on one end to a 0.5 mm radius hemisphere (instead of 0.3 mm). These changes were made simply for ease in fabrication of the shape of the end of the electrode by machining, since a thickness of 1.0 mm provides less flexibility than 0.6 mm. Parallel tests carried out with the thicker and thinner electrodes in SPINGS made from the same insulation composition verified that the same test results were obtained in each case. The test procedure using the thicker electrodes is therefore still referred to herein as Test Method A.
Examples 5 – 10
In these examples the insulation composition was similar to that of Examples 1-4; it was still a polyethylene homopolymer of density 0.918 grams/cc, but had a melt index of 2.5 and contained ca.750 ppm. of the same antioxidant, and different tree growth inhibitors were used.
In each case the amount of tree growth inhibitor in the polyethylene was 3% by weight.
In each of Examples 5 through 10 the tree growth inhibitor was added to polyethylene pellets by tumble blending followed by extrusion mixing. Four SPINGS were prepared for each example and placed on test using Test
Method A. (When four SPINGS are placed on test, the electrical endurance would be greater than the time for the second SPING to fail, but less than the time for the third SPING to fail.)
In Example 5, the tree growth inhibitor was n-dodecyl alcohol, a primary alcohol. All
SPINGS were removed from test after 600 hours. No SPINGS had failed. The electrical endurance was thus greater than 600 hours.
In Example 6, the tree growth inhibitor was cyclo-hexanol, a primary alcohol. All
SPINGS were removed from test after 768 hours. No SPINGS had failed. The electrical endurance was thus greater than 768 hours.
In Example 7, the tree growth inhibitor was benzyl alcohol, a primary alcohol. All
SPINGS were removed from test after 720 hours. No SPINGS had failed. The electrical endurance was greater than 720 hours.
In Example 8, the tree growth inhibitor was 2-decanol, a secondary alcohol. All
SPINGS were removed from test after 552 hours. No SPINGS had failed. The electrical endurance was greater than 552 hours.
In Example 9, the tree growth inhibitor was 4decanol, a secondary alcohol, All SPINGS were removed from test after 600 hours. No
SPINGS had failed. The electrical endurance was greater than 600 hours.
In Example 10, the tree growth inhibitor was 2-phenyl-2-propanol, a tertiary alcohol.
All SPINGS were removed from test after 552 hours. No SPINGS had failed. The electrical endurance was greater than 552 hours.
In all of Examples 5-10, the increase in electrical endurance compared with Control A is in excess of a thousand-fold.
Controls B, C and D
In Controls B to D, higher density polyethylene was tested.
Control B used polyethylene which has a density of 0.960 g/cc, and which contains 100 ppm “Irganox 10-10” antioxidant (“Irganox” is a Registered Trade Mark). The polyethylene pellets and 3% n-dodecyl alcohol were mixed by tumble blending, followed by extrusion mixing.
In Control C, 88.11% by weight of pellets of the same polyethylene of density 0.960 g/cc and 11.89% by weight of pellets of polyethylene of density 0.918 g/cc (which contains 700 ppm “Sanotox R” antioxidant) were tumble blended, further mixed by extrusion in a double-screw extruder, and pelletized.
Control D was similar except that 52.38% by weight of 0.960 density polyethylene and 47.62% by weight of 0.918 density polyethylene were used. In each case, the pellets of the blend were then tumble blended with 3% n-dodecyl alcohol, followed by extrusion mixing.
SPINGS of each composition were then fabricated for test purposes. A small chip of polymer was removed from one SPING of each composition to measure its density (ASTM D
1505-68). The densities were: Control B, 0.957 g/cc; Control C, 0.949 g/cc; and Control D, 0.936 glcc.
Five SPINGS of each composition were placed on test using Test Method A. In each of
Controls B, C and D, all five SPINGS failed be
fore one day had elapsed. Accordingly, the
electrical endurance in each case was less than
24 hours.
WHAT WE CLAIM IS:- 1. A composition suitable for use as
electrical insulation consisting essentially of:
(a) low density polyethylene or cross
linked low density polyethylene (both as
hereinbefore defined), and
(b) at least one monohydric alcohol of 6 to 24 carbon atoms, the alcohol being capable of producing at least a thousand-fold increase in electrical endurance of low density polyethylene as measured by Test Method A set out herein.
2. A composition according to claim 1 containing low density polyethylene and a peroxide crosslinking agent.
3. A composition according to claim 1 containing low density polyethylene but not a peroxide crosslinking agent.
4. A composition according to claim 1 containing cross-linked polyethylene which has been crosslinked by a peroxide crosslinking agent.
5. A composition according to any one of the preceding claims wherein the polymer (a) contains about 100 weight percent ethylene polymerised units.
6. A composition according to any one of the preceding claims with a power factor no greater than 0.5%.
7. A composition according to any one of the preceding claims wherein the alcohol is aliphatic.
8. A composition according to any one of the preceding claims wherein the alcohol contains 8 to 12 carbon atoms.
9. A composition according to claim 8 wherein the alcohol is n-decyl alcohol.
10. A composition according to claim 8 wherein the alcohol is n-dodecyl alcohol.
11. A composition according to any one of the preceding claims wherein the alcohol is present in an amount of 0.5 to 10% of the weight of the polymer (a).
12. A composition according to claim 11 wherein said amount is 1 to 5% by weight.
13. A composition according to claim 1
wherein the density of the polymer (a) is
about 0.918 g/cc.
14. A composition according to claim 1
substantially as described in any one of
Examples 1 to 10.
15. An article comprising an electrical
conductor and an insulating layer of a com
position as claimed in any one of the pre

Claims (1)

ceding claims.
16. An article according to claim 15 which is an electrical cable.
17. An article according to claim 15 or 16 which has a semiconducting layer between the electrical conductor and the insulating layer.
18. A process for preparing a composition as claimed in claim 2, which process comprises dissolving the peroxide crosslinking agent in the alcohol and adding the resulting solution to the low density polyethylene.
19. A process according to claim 18 wherein the alcohol is an alcohol of 8 to 12 carbon atoms.
20. A process according to claim 18 or 19 wherein the low density polyethylene has a
density of about 0.918 g/cc.

GB31443/77A
1976-07-28
1977-07-26
Electrical insulation compositions

Expired

GB1564990A
(en)

Applications Claiming Priority (2)

Application Number
Priority Date
Filing Date
Title

US70926676A

1976-07-28
1976-07-28

US80991077A

1977-06-28
1977-06-28

Publications (1)

Publication Number
Publication Date

GB1564990A
true

GB1564990A
(en)

1980-04-16

Family
ID=27108227
Family Applications (1)

Application Number
Title
Priority Date
Filing Date

GB31443/77A
Expired

GB1564990A
(en)

1976-07-28
1977-07-26
Electrical insulation compositions

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JP
(1)

JPS6034581B2
(en)

CA
(1)

CA1114979A
(en)

DE
(1)

DE2734071A1
(en)

FR
(1)

FR2360159A1
(en)

GB
(1)

GB1564990A
(en)

IT
(1)

IT1086163B
(en)

NL
(1)

NL7708334A
(en)

NO
(1)

NO150376C
(en)

SE
(2)

SE425911B
(en)

Cited By (1)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

WO2014206437A1
(en)

2013-06-24
2014-12-31
Abb Technology Ltd
A new process for preparing insulation materials for high voltage power applications and new insulation materials

Families Citing this family (8)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

DE2837311C2
(en)

1978-08-26
1983-11-24
Licentia Patent-Verwaltungs-Gmbh, 6000 Frankfurt

Voltage stabilized electrical insulation

US4283459A
(en)

1979-08-09
1981-08-11
E. I. Du Pont De Nemours And Company
Insulating composition and articles made therefrom

GB2076419B
(en)

1980-05-21
1984-01-25
Furukawa Electric Co Ltd
Cross-linked polyethylene insulated power cable

US4369331A
(en)

1980-12-22
1983-01-18
Union Carbide Corporation
Ethylene polymer compositions stabilized against water treeing by an organic titanate; and the use thereof as insulation about electrical conductors

DE3210139C2
(en)

1982-03-19
1985-06-27
Licentia Patent-Verwaltungs-Gmbh, 6000 Frankfurt

Polyolefin-based insulating material with voltage stabilizer

JPS58220304A
(en)

1982-06-15
1983-12-21
日立電線株式会社
Electrically insulating composition and wire, cable coated with same composition

DE3344759A1
(en)

1983-12-10
1985-06-20
Licentia Patent-Verwaltungs-Gmbh, 6000 Frankfurt
Stabilised polyolefin-based insulation material

JPS61264033A
(en)

1985-05-18
1986-11-21
Idemitsu Petrochem Co Ltd
Polyethylene resin composition

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Assignee
Title

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(en)

1957-07-26
1963-01-22
Siemens Ag
Method for improving the electric strength and flash-over or glowdischarge resistance of olefine polymers

DE1440097A1
(en)

1960-02-29
1968-10-24
Siemens Ag

Use of compounds based on olefin polymers for insulating electrical cables and lines

US3372153A
(en)

1965-04-09
1968-03-05
Union Carbide Corp
Polymer powders and process therefor

US3445394A
(en)

1967-06-27
1969-05-20
Simplex Wire & Cable Co
Voltage stabilized solid polyolefin dielectric

DE1615837A1
(en)

1968-01-12
1970-08-06
Basf Ag

Electrical insulating compounds based on olefin polymers

US3522183A
(en)

1968-05-07
1970-07-28
Simplex Wire & Cable Co
Solid dielectric polyolefin compositions containing various voltage stabilizers

DE1765583A1
(en)

1968-06-14
1971-07-29
Basf Ag

Electrical insulating compounds based on olefin polymers

DE2352450C2
(en)

1973-10-19
1982-05-13
Licentia Patent-Verwaltungs-Gmbh, 6000 Frankfurt

Stabilized insulating material based on polyolefin, in particular based on a cross-linked polyethylene

1977

1977-07-26
GB
GB31443/77A
patent/GB1564990A/en
not_active
Expired

1977-07-26
CA
CA283,549A
patent/CA1114979A/en
not_active
Expired

1977-07-27
SE
SE7708618A
patent/SE425911B/en
not_active
IP Right Cessation

1977-07-27
IT
IT26215/77A
patent/IT1086163B/en
active

1977-07-27
NL
NL7708334A
patent/NL7708334A/en
not_active
Application Discontinuation

1977-07-27
NO
NO772670A
patent/NO150376C/en
unknown

1977-07-27
FR
FR7723059A
patent/FR2360159A1/en
active
Granted

1977-07-27
JP
JP52089389A
patent/JPS6034581B2/en
not_active
Expired

1977-07-28
DE
DE19772734071
patent/DE2734071A1/en
not_active
Ceased

1982

1982-07-01
SE
SE8204087A
patent/SE8204087A0/en
unknown

Cited By (1)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

WO2014206437A1
(en)

2013-06-24
2014-12-31
Abb Technology Ltd
A new process for preparing insulation materials for high voltage power applications and new insulation materials

Also Published As

Publication number
Publication date

SE8204087A
(en)

1982-07-01

FR2360159A1
(en)

1978-02-24

SE8204087D0
(en)

1982-07-01

IT1086163B
(en)

1985-05-28

SE8204087A0
(en)

1982-07-01

NO150376B
(en)

1984-06-25

SE425911B
(en)

1982-11-22

FR2360159B1
(en)

1981-11-13

JPS6034581B2
(en)

1985-08-09

DE2734071A1
(en)

1978-02-02

NL7708334A
(en)

1978-01-31

NO150376C
(en)

1984-10-03

NO772670L
(en)

1978-01-31

JPS5316746A
(en)

1978-02-16

CA1114979A
(en)

1981-12-22

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