CA2332005A1 - Electrical cable having a self-sealing agent and method for preventing water from contacting the conductor - Google Patents
Electrical cable having a self-sealing agent and method for preventing water from contacting the conductor Download PDFInfo
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- CA2332005A1 CA2332005A1 CA002332005A CA2332005A CA2332005A1 CA 2332005 A1 CA2332005 A1 CA 2332005A1 CA 002332005 A CA002332005 A CA 002332005A CA 2332005 A CA2332005 A CA 2332005A CA 2332005 A1 CA2332005 A1 CA 2332005A1
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- cable
- conductor
- insulation
- installation
- electrical cable
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Links
- 239000004020 conductor Substances 0.000 title claims abstract description 96
- 238000007789 sealing Methods 0.000 title claims abstract description 13
- 238000000034 method Methods 0.000 title claims description 34
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims description 17
- 239000003795 chemical substances by application Substances 0.000 title description 2
- 239000000463 material Substances 0.000 claims abstract description 75
- 238000009413 insulation Methods 0.000 claims abstract description 54
- 230000035515 penetration Effects 0.000 claims abstract description 5
- 230000009969 flowable effect Effects 0.000 claims abstract 3
- 238000009434 installation Methods 0.000 claims description 18
- 229920002367 Polyisobutene Polymers 0.000 claims description 12
- 229920000642 polymer Polymers 0.000 claims description 11
- 238000004519 manufacturing process Methods 0.000 claims description 10
- 230000000694 effects Effects 0.000 claims description 6
- 239000003566 sealing material Substances 0.000 claims description 3
- 229910052782 aluminium Inorganic materials 0.000 description 18
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 17
- 230000007797 corrosion Effects 0.000 description 15
- 238000005260 corrosion Methods 0.000 description 15
- 238000012360 testing method Methods 0.000 description 14
- -1 aluminum ions Chemical class 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 8
- 238000001125 extrusion Methods 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 230000000903 blocking effect Effects 0.000 description 6
- 230000015556 catabolic process Effects 0.000 description 6
- 239000003518 caustics Substances 0.000 description 6
- 230000007547 defect Effects 0.000 description 6
- 239000000843 powder Substances 0.000 description 5
- 239000002689 soil Substances 0.000 description 5
- 230000004888 barrier function Effects 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 230000001681 protective effect Effects 0.000 description 4
- 239000000565 sealant Substances 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- 238000010276 construction Methods 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000005868 electrolysis reaction Methods 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 230000007246 mechanism Effects 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 229920003020 cross-linked polyethylene Polymers 0.000 description 2
- 239000004703 cross-linked polyethylene Substances 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 230000008439 repair process Effects 0.000 description 2
- 239000008399 tap water Substances 0.000 description 2
- 235000020679 tap water Nutrition 0.000 description 2
- 239000011800 void material Substances 0.000 description 2
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- 229910000881 Cu alloy Inorganic materials 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 239000004705 High-molecular-weight polyethylene Substances 0.000 description 1
- MXRIRQGCELJRSN-UHFFFAOYSA-N O.O.O.[Al] Chemical compound O.O.O.[Al] MXRIRQGCELJRSN-UHFFFAOYSA-N 0.000 description 1
- 238000012356 Product development Methods 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 238000009412 basement excavation Methods 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000007373 indentation Methods 0.000 description 1
- 230000004941 influx Effects 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 235000015110 jellies Nutrition 0.000 description 1
- 239000008274 jelly Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
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- 230000004048 modification Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A30/00—Adapting or protecting infrastructure or their operation
- Y02A30/14—Extreme weather resilient electric power supply systems, e.g. strengthening power lines or underground power cables
Landscapes
- Insulated Conductors (AREA)
Abstract
An electrical cable with a stranded central conductor encircled by insulation including a material which provides self sealing properties to the cable present at least between the adjacent edges of the stranded conductor and the insulation. Preferably, the material is a polymeric material which is flowable at a temperature at least as low as 25°C and has a 100 gram needle penetration value greater than 100 tenths of a millimeter at 25°
C.
C.
Description
ELECTRICAL CABLE HAVING A SELF-SEALING AGENT AND METHOD
FOR PREVENTING WATER FROM CONTACTING THE CONDUCTOR
FiACKGROUND OF THE IiYVENTION
Insulated solid and stranded electrical cables acre well known in the ant.
Generally s stranded cables include a central stranded conductor witl~~ a protecting insulation jacket disposed around the conductor.
The most frequent cause of failure of directly buried aluminum secondary csables is a cut or puncture in the insulation inflicted during or after installation. This leads to alternating current corrosion of the aluminum and finally to an open circuit. When a conductor is exposed to wet ~o soil, upon damage, leakage current may flow, and cause localized electrochemical conversion of aluminum to hydrated aluminum oxide and eventually to an open circuit of the conductor.
In the U.S., thousands of such instances occur annually and the repair (location, excavation, repair, and replacement) can be very costly. As a result of the failures and in response to this problem, a tougher insulation system was introduced and became an industry i s standard. The tougher cable is described as "ruggedizecl," and generally consists of two layers:
an inner layer of high molecular weight polyethylene and an outer Layer of high density polyethylene. This design is more resistant to mechanical damage than one pass crosslinked polyethylene, but still can result in exposure of the aluminum conductor if sufficient impact is involved.
2o Investigations show that AC electrolysis current can approach half wave;
rectification when the current density is high. This accounts for the rapid loss of aluminum metal frequently experienced in the field. A caustic solution (pH 10-12) develops at the aluminum surface and dissolves the protective oxide film.
The mechanism o:l'aluminum cable failure is the; formation of hydrous ahuninum oxide.
2s As the aluminum oxide solids build up, the insulation in the vicinity of the puncture is forced to swell and splits open, making larger areas of the aluminum conductor surface available for electrolysis, thus increasing the leakage current and accelerating the corrosion process. Rapid lass of aluminum by AC electrolysis continues until ultimately the cable is open-circuited. A
caustic environment is created at the aluminum, electrolyte interface, which dissolves the 3o protective oxide film.
'The ruggedized or abuse resistant type insulation was supposed to protect t:he cable from physical abuse. While it helped this problem, it did not eliminate 600 V cable failures. Utilities have recently reported v,~arying numbers of 600 V aluminum underground distribution cable failure rates scattered between 70 and 7000 per year. failures are evidenced by an open circuit 3s condition accompanied by severe corrosion of the alunninum conductor.
All the reasons for 600 V failures are unknown, l>ut several have been postulated by cable users. These cables seem to experience a high degree of infant mortality, followed by failures occurring over decades. 7"he infant mortalities are usually directly related to damage caused by LI'I~l 05778.4 adjacent utilities, damage inflicted by landscaping and pl'~anting, or damage to the cable prior to or during installation. The failures occurring years later are harder to explain. There have b~
postulations of lightning damage, manufacturing defects., or insulation degradation over the lne of the installation.
In order to better understand the insulation characteristics, studies of the AC' breakdown, and DC impulse breakdown were conducted. AC breakdown studies on several different cables showed a high safety margin of performance. Each of these cables had a 0.080 inch wall thickness. Tests were conducted in water filled conduits. The AC breakdown strength of all of these cables was consistently above 20 kV, far in excess of the operating stress.
io hnpulse breakdov~m studies have also been performed on several 600 V cable constructions having different insulation formulations. The impulse breakdown level of these cables was approximately 150 kV. This exceeds the BII. requirements of a 15 kV
cable system and should well exceed the impulses on 600 V secondary cables during operation.
T'he above margins of electrical performance were measured on new cables. They are far I s above what is needed to operate on a 600 V system since most of these cables operate at 120 V
to ground. One of the tests. during compound and product development is a long term insulation resistance test performed in water at the rated operating temperature of the insulation. For crosslinked polyethylene cables the water temperature is 90°C. The insulation re;>istance must demonstrate stability and ~be above minimum values for a minimum of twelve weeks. If there 2o is instability indicated, the test is continued indefinitely. Relative permittivity is measured at 80 v/mil and must meet specific values. Increase in capacitance and dissipation factor are also measured in 90°C water over a 14 day period. Insulation compounds used in present day cables easily meet these requirements.
Manufacturing defects in cable insulation are found during production by either of two zs methods. During the extrusion process, the cable is sent through a spark tester, where 28 kV DC, or l7kV AC, is applied to the insulation surface. Any manufacturing defect resulting in a hole in the insulation will initiate a discharge, which is detected by the spark tester. Most manufacturers use this method. Another test that is allso often employed is a full reel water immersion test. In this test 21 kV DC, or 7 kV AC is applied to the cable after immersion for 1 3o hour or 6 hours, depending on whether the cable is a plexed assembly or single conductor, respectively. The actual voltages used for these tests are dependent on the wall thickness. The above values are for an 0.080 inch wall.
The above testing Yeas demonstrated electrical performance that is stable and far surpasses the requirements ofthe installation for 600 V cable. This does not explain a sudden cable failure 3s after many years of operation. Such sudden failure can. be explained by a better understanding of the failure mechanism. Aluminum corrosion in the presence of an alternating leakage current is a combination of two different mechanisms. Alumirlum is normally afforded a great deal of corrosion protection by a relatively thin barrier layer of aluminum oxide, and a more permeable bulk layer of oxide. However, flaws or cracks exist in these layers which provides'. a spot for the 4o corrosion reaction to begin. The metal in contact with vvater undergoes an anodic (positive ions moving into solution) and a cathodic cycle, sixty times. per second.
LI'11105778.4 During the anodic halfcycle of leakage current, aluminum ions leave the metallic surf through these flaws and combine with hydroxyl ions in the water surrounding the cable. This reaction results in pitting of the metal and the formation of aluminum hydroxide., the whitish powder evident in corroded cables. Another important reaction also occurs. The hydroxyl ions s are attracted to the metal surface during this half cycle, wlhich. increases the pH, causing a caustic deterioration of the oxide layer, further exposing more aluminum.
During the cathodic half cycle another reaction occurs. Hydrogen ions are driven to the aluminum surface. Instead ofneutralizing the caustic hydroxyl concentration, the hydrogen ions combine and form hydrogen gas, which leaves the cable. The hydrogen depletion has the effect of further concentrating the caustic hydroxyl ions, thus fuuthering the deterioration o f the surface oxide. No pitting occurs during this half cycle since the aluminum ion is attracted to the metal.
A caustic solution develops, hydrogen evolves, aluminum pitting takes place, arid aluminum hydroxide forms during this reaction.
A critical current density is necessary to sustain the corrosion reaction.
Below this is current density corrosion will be very slight, or almost imperceptible.
Once the current density is high enough, the reaction can be swift. The necessary current density is below 1mA/in2. The current dlensity of a damaged 600 V cable is influenced by the voltage, leakage resistance, and the area of exposed metal. Variables affecting this can include dampness of the sail, chemistry of the soil, degree of damage, etc.
2o The toughest cables on the market today will not always stand up to the rigors of handling, installation, and operation. And exposed alunninum will eventually deteriorate. The solution, then, is to find a way to economically prevent the corrosion process.
Attempts have been made to prevent the ingress of moisture by introducing a sealant between the strands of the conductor and between the conductor and the insulation. See U.S. Pat.
2s Nos. 3,S~43,271 and 4,1317,450. However, it has been found that the mere introduction of a sealant into such spaces is not entirely satisfactory. Attempts to prevent moisture from reaching the conductor, such as using water swellable material, have not met with technical and/or economic success. For example, voids may be formed in the sealant during the application thereof or may be formed if the cable is accidentally punctured. Any such spaces or voids form 30 locations for the ingress of moisture which can lead to corrosion of the conductor and conventional sealants used in the cables cannot eliminate such voids.
A prior art attempt to minimize the flow of moisture or water within the interstitial spaces of a stranded conductor came in the form of compacted or compressed stranded conductors. The stranded conductor itself waa radially crushed in order to reduce the diameter of l:he conductor 3s and to fill the interstitial spacing with metal from the indiividual wires themselves. 'Che drawback to this method is that even. though some deformation of the individual wires does take place, and some of the interstitial spacing is filled, there is still the possibility of cable insulation damage through which moisture can enter the cable and contact the conductor.
Another attempt at correcting moisture flowing within interstitial space;
consisted of 4o filling the interstitial space with a foreign substance which physically prevented tl~e flow of the L!'1~ I 05778.4 moisture or water within the conductor structure. These substances typically comprised some type of jelly base and a polyethylene filler material. .At slightly elevated temperatures, compound becomes fluid and viscous and can be applied as the conductor is being formed. The individual wires used to fbrm the conductor are fed unto an extrusion die where the moisture s blocking compound is extruded onto and around each individual wire and, as the wires are stranded into the conductor, the interstitial space is filled with the jelly-like material. Upon cooling, the filler becomes very stable and immobile and does not flow out of the interstitial spaces of the stranded conductor. Once the filling compound is applied within the interstitial spaces of the stranded conductor, it tends to remain in place. The problems encountered in io applying such a filling substance revolve around precise metering of the material into the interstitial spaces as the stranded conductor is being folnned. If too much material is extruded into the conductor, the outer insulation will not fit properly. If too little material i.s applied, the interstitial spaces will not be filled and therefore will allow moisture to flow within the conductor.
is Another drawback to this method of applying .a moisture blocking material is that an extrusion head and an extrusion pump for applying the material is required for every individual layer of wires used to form the conductor. The problems described above regarding the regulation of the volume of material applied through an extrusion head are multiplied every time an additional extrusion pump and extrusion head is required within the conductor manufacturing 2o system. Prior art efforts to manufacture an acceptable; moisture blocked conductor revolved around methods for uniform application of the moisture. blocking material to the conductor, but did not solve the problems created by handling and installation damage.
Applications of moisture blocking material to tlhe spacing of concentric lay conductors is known within the indu:;try. This can be found in United States Patents numbered 3,607,487;
2s 3,889,465; 4,105,485; 4,1.29,466; 4,435,613; 4,563,540; and 4,273,597.
~U.S. Patent 4,27;4,597 shows a method of strand filling the interstitial spacing of a conductor with a powder. This is accomplished by passing the strands throul;h a fluidized powder bed, where the interstitial spacing is filled with t:he powder. The stranded conductor then exits the opposite end of the bed where an insulating layer is applied which prevents the powder 3o from vacating the interstitial spacing of the conductor.
U.S. Patent 4,563,540 describes a conductor which is constructed by flooding a waterproofing material among the individual conductors which make up the core of the stranded conductor. This flooded core is then wrapped with a plurality of different layers of shielding material which prevents the influx of moisture into the stranded conductor.
3s U.S. Patent 4,435,613 describes a conductor constructed of a plurality of layers of insulating material with t:he core (or conducting portion) of the conductor being filled with an insulating layer ofpolyethylene. This polyethylene layer is contained by other rublber and plastic and epoxy compounds which produce a conductor having a waterproof construction.
U.S. Patent 4,129,466 deals with a method for the application of the filling medium ao which is applied to a stranded conductor. This method comprises a chamber into which are passed individual wires that will be used to form the stranded conductor.
These; wires have a LI'1~ I 05778.4 filling medium applied to them in the chamber. After the application of this filling ;medium, the conductor is passed through a chilling chamber where the filling medium is cooled and allov~
to solidify within the interstitial spaces. This method requires that the chamber containing tin filling medium and the stranded conductor be both heated and pressurized. The heat applied to the chamber reduces the viscosity of the filling material, while the pressure assures introduction of the material into the interstitial spaces of the strandef~ conductor.
U.S. Patent 4,105,485 deals with the apparatus utilized in the '466 method patent previously discussed.
U~.S. Patent 3,889,455 discloses a method and apparatus for filling the interstitial spacing t o of the stranded conductor in a high temperature flooding tank. The individual wires are fed into a tank containing the filling material, the material havin~; been heated to allow it to become less viscous. The individual wires are stranded and closed vrithin the confines of the flooding tank and the finished conductor is withdrawn from the opposite end of the flooding tank where it is passed through a cooling means. The disadvantages e~;perienced here involve th.e practice of t s stranding the conductor beneath the surface of an elevated temperature moisture block pool. No access, either visual or mechanical, to the conductor manufacturing process is practical.
U. S. Patent 3,607,4.87 describes a method whereby individual strands of wire are fed into a flooding tank which is supplied with heated filling material by a pump and an inj c;ction means.
The stranded conductor is withdrawn through the opposite end of the flooding tank, wiped in a 2o wiping die, wrapped in a core wrapper and then passed through a binder where it is bound. The bound, wrapped core is thc;n passed through a cooler which sets the filling material. The above described process is repeated through another flooding; tank, another cooler, another binding machines another flooding tank, another extruder, another cooling trough, and is eventually withdrawn from the end of the manufacturing line as a product having a pluralit~,~ of layers of 2s moisture blocking compound which protects the conductor core. The disadvantages here comprise a complex manufacturing line whereby moistmre blocking material is applied at many different locations, each having to be meticulously monitored and controlled in order for a proper conductor construction to be obtained.
It can be readily seen from the above referenced methods and apparatuses that moisture 3o blocked conductors are known and it can also be recognized that there are major problems concerning the elimination of moisture contacting the conductor as a result of .handling and installation of a cable.
flIEZIEF SUMMARY OF THE. INVENTION
The present invention relates to improvements i.n insulated solid and stranded cables.
3s In one embodiment of the invention, during rr~anufacture of the self sealing cable, a material which provides the cable with puncture, crack, and void self sealing properties is included between the conductor and the insulation. An additional water barrier material may also be included between the insulator and the conductor. Preferably, both materials aJre included in the cable. In this way, not only are the voids filled by the: material, but the material will flow into L171105778.4 any void, puncture, or crack formed in the insulation, thus lpreventing migration of moisture, with the added safety of the additional water barrier. When an additional water barnc;r, such a;
polymer sheet or film, is used, the self sealing material is applied over such barrier between the barner and the insulation, in which case the self sealing material does not contact the conductor.
Tile objects and advantages ofthe invention will be apparent from the follov~ring detailed description of the preferred embodiments thereof in conjunction with the accompanying drawings in which:
FIG. 1 is a cut-away, perspective view of a cable of the invention showing a stranded to conductor, the insulation, and the material which provides the self sealing effect;
FIG. 2 is an end view of the embodiment of the cable shown in FIG. l; arid FIG 3 is an end view of the cable shown in FIG. 2 having a break in the insulation with the break sealed by the material.
DETAILED DESCRIPTION IN T'HE INVENTION
~s Although the principles of the present invention are applicable to different types of electric cables, the invention will be described in connection with a known cable structure, such as a 600 volt cable, which normally comprises, as a minimum:
(1) A central conductor of stranded wires of a good conductivity metal such as copper, aluminum, copper alloys or aluminum alloys; and 20 (2) A layer of insulation around the stranded conductors which has been extruded thereover.
FIG. 1 shows a cable 11 comprising a conductor 12 of stranded wires of copper or aluminum or alloys thereof. A layer 10 of material 'which provides the self sealing effect encircles the conductor 12 and fills any spaces between conductor 12 and an insulation jacket 13 2s which encircles material 10 and conductor 12. Insulation jacket 13 is of known material and is preferably an extruded polymeric material.
Preferred material 10 comprises a polymer which can be readily pumped at temperatures at least as low as 25°C. Preferably, the polymer will be; a low molecular weight polymer such as low molecular weight i comer. Other materials, or combinations of materials, with or without 3o such polymers, having such characteristics may also ibe useful in the present invention. A
polymer which has been found to be particularly suitable is polyisobutene.
The preferred polymer of the present invention has very little or no significant Shore A
hardness. A test of determining whether or not the polymer has acceptable properties is the L171105778.4 Penetrometer Test incorporated in ASTM DS Penetration of Bituminous Materials.
The 100 grams needle penetration 'value at 25°C should be greatc;r than about 100 tenths of a millimet The material used to provide the self sealing ei~fect to the electric cable of the present invention has the following properties:
(a) The materiial is substantially insoluble in water;
(b) The material is a dielectric, i.e., it is non-conductive and is not a semi-conductor;
(c) The material causes the cable to be self sealing, i.e., it will flow, at ambient temperatuhe, into insulation voids and/o1~ cracks and prevent contact between the conductor and moisture which could cause cable failure; and to (d) The material does not absorb moisture or swell upon contact with moisture.
In the preferred embodiment of the present invention, the material used to fill the space between the conductor and the insulation is a compound of low molecular weight isomer or a low molecular weight copolymer of an isomer. Preferably, the material is polyisobutene.
Advantageously there is little or no air present in thc~ cable between the conductor and the is insulation.
The material of rthe present invention may optionally contain filler material, but is essentially free of any solvents or oils.
The cable 11 described in connection with FIG. 1 can be used without further layers encircling the insulation jacket 13.
zo Also, in other embodiments of the present invention described herein, the conductor and layers df insulation can 'be the same as those described in connection with FIG. 1.
The cable 14 illustrated in FIG. 2 is an end view of cable 11 illustrated in FIG. 1.
FIG. 3 is an end view of cable 11 shown in FICi. 1 and illustrates the self=sealing effect of material 10 which flows into a break in insulation 13, thereby preventing :moisture from 2s coming into contact with conductor 12.
It is to be understood that in the embodiments described which include afditional layers of protective material between the conductor and the insulation jacket, including an additional water barner of a polymer sheet or film, it is not essential that the j acket tightly enclose the layers there within or enter into the spaces between the wires .and protective materials, i.e., the interior 3o size of the jacket can be essentially equal to the exterior size of the elongated elements so that compression of the elongated elements, and hence, indentation of the layers there within including the insulation, is prevented.
The cable of the present invention is of particular advantage in that not;
only does the material fill the space between the conductor and the insulation as the cable is maa~ufactured, but LI11105778.4 after the cable is placed in service the material will f<ow into any cuts or punctures formed as a result of damage during handling and installation of the cable or its use in service. The stress placed on the conductor and the insulation during handling and installation of the cable, such as bending, stretching, reeling and unreeling, striking with digging and installation equipment can form cuts or punctures in the insulation and between the insulation and the conductcir. Such cuts or punctures can also be formed after the cable has been placed in service as a result of damage from adjacent utilities, honner owners, or lightening strikes. As can be seen from the Example, the cable of the present invention can provide acceptable service even after the insulation has been cut ~or punctured, exposing the conductor.
io Li'1~105778.4 Defects which exposed the conductor were made in the insulation layer of two cable samples. On one of the cable samples, a layer of polyisobutene polymer had been applied to the surface of the conductor. The other cable sample. did not have the polyisobutene layer.
Both cable samples were placed inside separate 1 liter glass beakers containing tap water. Each cable sample was energized at 1 l OV to ground with AC current. The sample-which did not have the polyisobutene layer exhibited severe corrosion overnight. The sample containing the polyisobutene layer exhibited no corrosion after being energized and submerged for 4 weeks in tap water in the glass beaker.
to Although preferred embodiments of the present invention have been described and illustrated, it will be apparent to those skilled in the art that various modifications may be made without departing from the principles of the invention.
The conductors from seven 600 V cable samples .approximately 12 inches in length were I s coated with the polyisobutylene. A defect was made in the middle of each sample which exposed the conductor. Three untreated cables (without polyisobutylene) were similarly damaged to expose the conductor. Each of the cable samples was them placed inside a laboratory rectangular soil box., across and through the long sides of the box, which was then filled with soil. Each sample was energized at 1 l OV to ground. The soil box 'was periodically watered vto insure that 2o the conditions leading to AC corrosion were present. Drleasurements of leakage current were taken to monitor the effect of the polyisobutylene layer on preventing corrosion. Periodically, the ability of each sample to carry 20 amps AC current was tested. Over a period of 2 months, all of the untreated cables showed increasing levels of current leakage, indicating; progressive corrosion. The ability of the untreated samples to carry current deteriorated rapidly during this 2s period. At the end of two months, untreated sample #1 was unable to carry more tlhan 0.5 amps AC current. Untreated sample #2 could carry only 12.2 amps while untreated cable #3 could carry no .more than 9.6 amps. Current leakage from the untreated samples increased steadily over the 2 month test span from a low of 0.32 mA up to a high of 353 mA. In contrast:, none of the treated samples showed a current leakage greater than 4'7.6 mA. After the initial reading on this 3o sample showing 47.6 mA, the polyisobutylene apparently sealed the defect as indicated by a drop in the current leakage to 0.37 mA at the end ofthe 2 month test period. The other treated samples showed similar results,.he~wever most never showed leakage current over 0.5 mA. In addition, all of the treated samples continued to carry 20 amps current at the end of the 2 month test period.
LIT1105778.4
FOR PREVENTING WATER FROM CONTACTING THE CONDUCTOR
FiACKGROUND OF THE IiYVENTION
Insulated solid and stranded electrical cables acre well known in the ant.
Generally s stranded cables include a central stranded conductor witl~~ a protecting insulation jacket disposed around the conductor.
The most frequent cause of failure of directly buried aluminum secondary csables is a cut or puncture in the insulation inflicted during or after installation. This leads to alternating current corrosion of the aluminum and finally to an open circuit. When a conductor is exposed to wet ~o soil, upon damage, leakage current may flow, and cause localized electrochemical conversion of aluminum to hydrated aluminum oxide and eventually to an open circuit of the conductor.
In the U.S., thousands of such instances occur annually and the repair (location, excavation, repair, and replacement) can be very costly. As a result of the failures and in response to this problem, a tougher insulation system was introduced and became an industry i s standard. The tougher cable is described as "ruggedizecl," and generally consists of two layers:
an inner layer of high molecular weight polyethylene and an outer Layer of high density polyethylene. This design is more resistant to mechanical damage than one pass crosslinked polyethylene, but still can result in exposure of the aluminum conductor if sufficient impact is involved.
2o Investigations show that AC electrolysis current can approach half wave;
rectification when the current density is high. This accounts for the rapid loss of aluminum metal frequently experienced in the field. A caustic solution (pH 10-12) develops at the aluminum surface and dissolves the protective oxide film.
The mechanism o:l'aluminum cable failure is the; formation of hydrous ahuninum oxide.
2s As the aluminum oxide solids build up, the insulation in the vicinity of the puncture is forced to swell and splits open, making larger areas of the aluminum conductor surface available for electrolysis, thus increasing the leakage current and accelerating the corrosion process. Rapid lass of aluminum by AC electrolysis continues until ultimately the cable is open-circuited. A
caustic environment is created at the aluminum, electrolyte interface, which dissolves the 3o protective oxide film.
'The ruggedized or abuse resistant type insulation was supposed to protect t:he cable from physical abuse. While it helped this problem, it did not eliminate 600 V cable failures. Utilities have recently reported v,~arying numbers of 600 V aluminum underground distribution cable failure rates scattered between 70 and 7000 per year. failures are evidenced by an open circuit 3s condition accompanied by severe corrosion of the alunninum conductor.
All the reasons for 600 V failures are unknown, l>ut several have been postulated by cable users. These cables seem to experience a high degree of infant mortality, followed by failures occurring over decades. 7"he infant mortalities are usually directly related to damage caused by LI'I~l 05778.4 adjacent utilities, damage inflicted by landscaping and pl'~anting, or damage to the cable prior to or during installation. The failures occurring years later are harder to explain. There have b~
postulations of lightning damage, manufacturing defects., or insulation degradation over the lne of the installation.
In order to better understand the insulation characteristics, studies of the AC' breakdown, and DC impulse breakdown were conducted. AC breakdown studies on several different cables showed a high safety margin of performance. Each of these cables had a 0.080 inch wall thickness. Tests were conducted in water filled conduits. The AC breakdown strength of all of these cables was consistently above 20 kV, far in excess of the operating stress.
io hnpulse breakdov~m studies have also been performed on several 600 V cable constructions having different insulation formulations. The impulse breakdown level of these cables was approximately 150 kV. This exceeds the BII. requirements of a 15 kV
cable system and should well exceed the impulses on 600 V secondary cables during operation.
T'he above margins of electrical performance were measured on new cables. They are far I s above what is needed to operate on a 600 V system since most of these cables operate at 120 V
to ground. One of the tests. during compound and product development is a long term insulation resistance test performed in water at the rated operating temperature of the insulation. For crosslinked polyethylene cables the water temperature is 90°C. The insulation re;>istance must demonstrate stability and ~be above minimum values for a minimum of twelve weeks. If there 2o is instability indicated, the test is continued indefinitely. Relative permittivity is measured at 80 v/mil and must meet specific values. Increase in capacitance and dissipation factor are also measured in 90°C water over a 14 day period. Insulation compounds used in present day cables easily meet these requirements.
Manufacturing defects in cable insulation are found during production by either of two zs methods. During the extrusion process, the cable is sent through a spark tester, where 28 kV DC, or l7kV AC, is applied to the insulation surface. Any manufacturing defect resulting in a hole in the insulation will initiate a discharge, which is detected by the spark tester. Most manufacturers use this method. Another test that is allso often employed is a full reel water immersion test. In this test 21 kV DC, or 7 kV AC is applied to the cable after immersion for 1 3o hour or 6 hours, depending on whether the cable is a plexed assembly or single conductor, respectively. The actual voltages used for these tests are dependent on the wall thickness. The above values are for an 0.080 inch wall.
The above testing Yeas demonstrated electrical performance that is stable and far surpasses the requirements ofthe installation for 600 V cable. This does not explain a sudden cable failure 3s after many years of operation. Such sudden failure can. be explained by a better understanding of the failure mechanism. Aluminum corrosion in the presence of an alternating leakage current is a combination of two different mechanisms. Alumirlum is normally afforded a great deal of corrosion protection by a relatively thin barrier layer of aluminum oxide, and a more permeable bulk layer of oxide. However, flaws or cracks exist in these layers which provides'. a spot for the 4o corrosion reaction to begin. The metal in contact with vvater undergoes an anodic (positive ions moving into solution) and a cathodic cycle, sixty times. per second.
LI'11105778.4 During the anodic halfcycle of leakage current, aluminum ions leave the metallic surf through these flaws and combine with hydroxyl ions in the water surrounding the cable. This reaction results in pitting of the metal and the formation of aluminum hydroxide., the whitish powder evident in corroded cables. Another important reaction also occurs. The hydroxyl ions s are attracted to the metal surface during this half cycle, wlhich. increases the pH, causing a caustic deterioration of the oxide layer, further exposing more aluminum.
During the cathodic half cycle another reaction occurs. Hydrogen ions are driven to the aluminum surface. Instead ofneutralizing the caustic hydroxyl concentration, the hydrogen ions combine and form hydrogen gas, which leaves the cable. The hydrogen depletion has the effect of further concentrating the caustic hydroxyl ions, thus fuuthering the deterioration o f the surface oxide. No pitting occurs during this half cycle since the aluminum ion is attracted to the metal.
A caustic solution develops, hydrogen evolves, aluminum pitting takes place, arid aluminum hydroxide forms during this reaction.
A critical current density is necessary to sustain the corrosion reaction.
Below this is current density corrosion will be very slight, or almost imperceptible.
Once the current density is high enough, the reaction can be swift. The necessary current density is below 1mA/in2. The current dlensity of a damaged 600 V cable is influenced by the voltage, leakage resistance, and the area of exposed metal. Variables affecting this can include dampness of the sail, chemistry of the soil, degree of damage, etc.
2o The toughest cables on the market today will not always stand up to the rigors of handling, installation, and operation. And exposed alunninum will eventually deteriorate. The solution, then, is to find a way to economically prevent the corrosion process.
Attempts have been made to prevent the ingress of moisture by introducing a sealant between the strands of the conductor and between the conductor and the insulation. See U.S. Pat.
2s Nos. 3,S~43,271 and 4,1317,450. However, it has been found that the mere introduction of a sealant into such spaces is not entirely satisfactory. Attempts to prevent moisture from reaching the conductor, such as using water swellable material, have not met with technical and/or economic success. For example, voids may be formed in the sealant during the application thereof or may be formed if the cable is accidentally punctured. Any such spaces or voids form 30 locations for the ingress of moisture which can lead to corrosion of the conductor and conventional sealants used in the cables cannot eliminate such voids.
A prior art attempt to minimize the flow of moisture or water within the interstitial spaces of a stranded conductor came in the form of compacted or compressed stranded conductors. The stranded conductor itself waa radially crushed in order to reduce the diameter of l:he conductor 3s and to fill the interstitial spacing with metal from the indiividual wires themselves. 'Che drawback to this method is that even. though some deformation of the individual wires does take place, and some of the interstitial spacing is filled, there is still the possibility of cable insulation damage through which moisture can enter the cable and contact the conductor.
Another attempt at correcting moisture flowing within interstitial space;
consisted of 4o filling the interstitial space with a foreign substance which physically prevented tl~e flow of the L!'1~ I 05778.4 moisture or water within the conductor structure. These substances typically comprised some type of jelly base and a polyethylene filler material. .At slightly elevated temperatures, compound becomes fluid and viscous and can be applied as the conductor is being formed. The individual wires used to fbrm the conductor are fed unto an extrusion die where the moisture s blocking compound is extruded onto and around each individual wire and, as the wires are stranded into the conductor, the interstitial space is filled with the jelly-like material. Upon cooling, the filler becomes very stable and immobile and does not flow out of the interstitial spaces of the stranded conductor. Once the filling compound is applied within the interstitial spaces of the stranded conductor, it tends to remain in place. The problems encountered in io applying such a filling substance revolve around precise metering of the material into the interstitial spaces as the stranded conductor is being folnned. If too much material is extruded into the conductor, the outer insulation will not fit properly. If too little material i.s applied, the interstitial spaces will not be filled and therefore will allow moisture to flow within the conductor.
is Another drawback to this method of applying .a moisture blocking material is that an extrusion head and an extrusion pump for applying the material is required for every individual layer of wires used to form the conductor. The problems described above regarding the regulation of the volume of material applied through an extrusion head are multiplied every time an additional extrusion pump and extrusion head is required within the conductor manufacturing 2o system. Prior art efforts to manufacture an acceptable; moisture blocked conductor revolved around methods for uniform application of the moisture. blocking material to the conductor, but did not solve the problems created by handling and installation damage.
Applications of moisture blocking material to tlhe spacing of concentric lay conductors is known within the indu:;try. This can be found in United States Patents numbered 3,607,487;
2s 3,889,465; 4,105,485; 4,1.29,466; 4,435,613; 4,563,540; and 4,273,597.
~U.S. Patent 4,27;4,597 shows a method of strand filling the interstitial spacing of a conductor with a powder. This is accomplished by passing the strands throul;h a fluidized powder bed, where the interstitial spacing is filled with t:he powder. The stranded conductor then exits the opposite end of the bed where an insulating layer is applied which prevents the powder 3o from vacating the interstitial spacing of the conductor.
U.S. Patent 4,563,540 describes a conductor which is constructed by flooding a waterproofing material among the individual conductors which make up the core of the stranded conductor. This flooded core is then wrapped with a plurality of different layers of shielding material which prevents the influx of moisture into the stranded conductor.
3s U.S. Patent 4,435,613 describes a conductor constructed of a plurality of layers of insulating material with t:he core (or conducting portion) of the conductor being filled with an insulating layer ofpolyethylene. This polyethylene layer is contained by other rublber and plastic and epoxy compounds which produce a conductor having a waterproof construction.
U.S. Patent 4,129,466 deals with a method for the application of the filling medium ao which is applied to a stranded conductor. This method comprises a chamber into which are passed individual wires that will be used to form the stranded conductor.
These; wires have a LI'1~ I 05778.4 filling medium applied to them in the chamber. After the application of this filling ;medium, the conductor is passed through a chilling chamber where the filling medium is cooled and allov~
to solidify within the interstitial spaces. This method requires that the chamber containing tin filling medium and the stranded conductor be both heated and pressurized. The heat applied to the chamber reduces the viscosity of the filling material, while the pressure assures introduction of the material into the interstitial spaces of the strandef~ conductor.
U.S. Patent 4,105,485 deals with the apparatus utilized in the '466 method patent previously discussed.
U~.S. Patent 3,889,455 discloses a method and apparatus for filling the interstitial spacing t o of the stranded conductor in a high temperature flooding tank. The individual wires are fed into a tank containing the filling material, the material havin~; been heated to allow it to become less viscous. The individual wires are stranded and closed vrithin the confines of the flooding tank and the finished conductor is withdrawn from the opposite end of the flooding tank where it is passed through a cooling means. The disadvantages e~;perienced here involve th.e practice of t s stranding the conductor beneath the surface of an elevated temperature moisture block pool. No access, either visual or mechanical, to the conductor manufacturing process is practical.
U. S. Patent 3,607,4.87 describes a method whereby individual strands of wire are fed into a flooding tank which is supplied with heated filling material by a pump and an inj c;ction means.
The stranded conductor is withdrawn through the opposite end of the flooding tank, wiped in a 2o wiping die, wrapped in a core wrapper and then passed through a binder where it is bound. The bound, wrapped core is thc;n passed through a cooler which sets the filling material. The above described process is repeated through another flooding; tank, another cooler, another binding machines another flooding tank, another extruder, another cooling trough, and is eventually withdrawn from the end of the manufacturing line as a product having a pluralit~,~ of layers of 2s moisture blocking compound which protects the conductor core. The disadvantages here comprise a complex manufacturing line whereby moistmre blocking material is applied at many different locations, each having to be meticulously monitored and controlled in order for a proper conductor construction to be obtained.
It can be readily seen from the above referenced methods and apparatuses that moisture 3o blocked conductors are known and it can also be recognized that there are major problems concerning the elimination of moisture contacting the conductor as a result of .handling and installation of a cable.
flIEZIEF SUMMARY OF THE. INVENTION
The present invention relates to improvements i.n insulated solid and stranded cables.
3s In one embodiment of the invention, during rr~anufacture of the self sealing cable, a material which provides the cable with puncture, crack, and void self sealing properties is included between the conductor and the insulation. An additional water barrier material may also be included between the insulator and the conductor. Preferably, both materials aJre included in the cable. In this way, not only are the voids filled by the: material, but the material will flow into L171105778.4 any void, puncture, or crack formed in the insulation, thus lpreventing migration of moisture, with the added safety of the additional water barrier. When an additional water barnc;r, such a;
polymer sheet or film, is used, the self sealing material is applied over such barrier between the barner and the insulation, in which case the self sealing material does not contact the conductor.
Tile objects and advantages ofthe invention will be apparent from the follov~ring detailed description of the preferred embodiments thereof in conjunction with the accompanying drawings in which:
FIG. 1 is a cut-away, perspective view of a cable of the invention showing a stranded to conductor, the insulation, and the material which provides the self sealing effect;
FIG. 2 is an end view of the embodiment of the cable shown in FIG. l; arid FIG 3 is an end view of the cable shown in FIG. 2 having a break in the insulation with the break sealed by the material.
DETAILED DESCRIPTION IN T'HE INVENTION
~s Although the principles of the present invention are applicable to different types of electric cables, the invention will be described in connection with a known cable structure, such as a 600 volt cable, which normally comprises, as a minimum:
(1) A central conductor of stranded wires of a good conductivity metal such as copper, aluminum, copper alloys or aluminum alloys; and 20 (2) A layer of insulation around the stranded conductors which has been extruded thereover.
FIG. 1 shows a cable 11 comprising a conductor 12 of stranded wires of copper or aluminum or alloys thereof. A layer 10 of material 'which provides the self sealing effect encircles the conductor 12 and fills any spaces between conductor 12 and an insulation jacket 13 2s which encircles material 10 and conductor 12. Insulation jacket 13 is of known material and is preferably an extruded polymeric material.
Preferred material 10 comprises a polymer which can be readily pumped at temperatures at least as low as 25°C. Preferably, the polymer will be; a low molecular weight polymer such as low molecular weight i comer. Other materials, or combinations of materials, with or without 3o such polymers, having such characteristics may also ibe useful in the present invention. A
polymer which has been found to be particularly suitable is polyisobutene.
The preferred polymer of the present invention has very little or no significant Shore A
hardness. A test of determining whether or not the polymer has acceptable properties is the L171105778.4 Penetrometer Test incorporated in ASTM DS Penetration of Bituminous Materials.
The 100 grams needle penetration 'value at 25°C should be greatc;r than about 100 tenths of a millimet The material used to provide the self sealing ei~fect to the electric cable of the present invention has the following properties:
(a) The materiial is substantially insoluble in water;
(b) The material is a dielectric, i.e., it is non-conductive and is not a semi-conductor;
(c) The material causes the cable to be self sealing, i.e., it will flow, at ambient temperatuhe, into insulation voids and/o1~ cracks and prevent contact between the conductor and moisture which could cause cable failure; and to (d) The material does not absorb moisture or swell upon contact with moisture.
In the preferred embodiment of the present invention, the material used to fill the space between the conductor and the insulation is a compound of low molecular weight isomer or a low molecular weight copolymer of an isomer. Preferably, the material is polyisobutene.
Advantageously there is little or no air present in thc~ cable between the conductor and the is insulation.
The material of rthe present invention may optionally contain filler material, but is essentially free of any solvents or oils.
The cable 11 described in connection with FIG. 1 can be used without further layers encircling the insulation jacket 13.
zo Also, in other embodiments of the present invention described herein, the conductor and layers df insulation can 'be the same as those described in connection with FIG. 1.
The cable 14 illustrated in FIG. 2 is an end view of cable 11 illustrated in FIG. 1.
FIG. 3 is an end view of cable 11 shown in FICi. 1 and illustrates the self=sealing effect of material 10 which flows into a break in insulation 13, thereby preventing :moisture from 2s coming into contact with conductor 12.
It is to be understood that in the embodiments described which include afditional layers of protective material between the conductor and the insulation jacket, including an additional water barner of a polymer sheet or film, it is not essential that the j acket tightly enclose the layers there within or enter into the spaces between the wires .and protective materials, i.e., the interior 3o size of the jacket can be essentially equal to the exterior size of the elongated elements so that compression of the elongated elements, and hence, indentation of the layers there within including the insulation, is prevented.
The cable of the present invention is of particular advantage in that not;
only does the material fill the space between the conductor and the insulation as the cable is maa~ufactured, but LI11105778.4 after the cable is placed in service the material will f<ow into any cuts or punctures formed as a result of damage during handling and installation of the cable or its use in service. The stress placed on the conductor and the insulation during handling and installation of the cable, such as bending, stretching, reeling and unreeling, striking with digging and installation equipment can form cuts or punctures in the insulation and between the insulation and the conductcir. Such cuts or punctures can also be formed after the cable has been placed in service as a result of damage from adjacent utilities, honner owners, or lightening strikes. As can be seen from the Example, the cable of the present invention can provide acceptable service even after the insulation has been cut ~or punctured, exposing the conductor.
io Li'1~105778.4 Defects which exposed the conductor were made in the insulation layer of two cable samples. On one of the cable samples, a layer of polyisobutene polymer had been applied to the surface of the conductor. The other cable sample. did not have the polyisobutene layer.
Both cable samples were placed inside separate 1 liter glass beakers containing tap water. Each cable sample was energized at 1 l OV to ground with AC current. The sample-which did not have the polyisobutene layer exhibited severe corrosion overnight. The sample containing the polyisobutene layer exhibited no corrosion after being energized and submerged for 4 weeks in tap water in the glass beaker.
to Although preferred embodiments of the present invention have been described and illustrated, it will be apparent to those skilled in the art that various modifications may be made without departing from the principles of the invention.
The conductors from seven 600 V cable samples .approximately 12 inches in length were I s coated with the polyisobutylene. A defect was made in the middle of each sample which exposed the conductor. Three untreated cables (without polyisobutylene) were similarly damaged to expose the conductor. Each of the cable samples was them placed inside a laboratory rectangular soil box., across and through the long sides of the box, which was then filled with soil. Each sample was energized at 1 l OV to ground. The soil box 'was periodically watered vto insure that 2o the conditions leading to AC corrosion were present. Drleasurements of leakage current were taken to monitor the effect of the polyisobutylene layer on preventing corrosion. Periodically, the ability of each sample to carry 20 amps AC current was tested. Over a period of 2 months, all of the untreated cables showed increasing levels of current leakage, indicating; progressive corrosion. The ability of the untreated samples to carry current deteriorated rapidly during this 2s period. At the end of two months, untreated sample #1 was unable to carry more tlhan 0.5 amps AC current. Untreated sample #2 could carry only 12.2 amps while untreated cable #3 could carry no .more than 9.6 amps. Current leakage from the untreated samples increased steadily over the 2 month test span from a low of 0.32 mA up to a high of 353 mA. In contrast:, none of the treated samples showed a current leakage greater than 4'7.6 mA. After the initial reading on this 3o sample showing 47.6 mA, the polyisobutylene apparently sealed the defect as indicated by a drop in the current leakage to 0.37 mA at the end ofthe 2 month test period. The other treated samples showed similar results,.he~wever most never showed leakage current over 0.5 mA. In addition, all of the treated samples continued to carry 20 amps current at the end of the 2 month test period.
LIT1105778.4
Claims (25)
1. An electrical cable comprising a conductor, a layer of insulation around said conductor and a material between the conductor and thc; insulation which providers self sealing properties to the cable.
2. The electrical cable of claim 1 wherein said material is a dielectric.
3. The electrical cable of claim 2 wherein said material is flowable at about 25°C.
4. The electriical cable of claim 4 wherein said material has a 100 gram needle penetration value greater than 100 tenths of a millimeter at 25°C.
5. The electrical cable of claim 4 wherein said material is a polymeric material.
6. The electrical cable of claim 5 wherein said material is an isomer.
7. The electrical cable of claim 6 wherein aaid material is polyisobutene.
8. The electrical cable of claim 1 wherein the conductor is formed by a plurality of wires stranded together.
9. An electrical cable as set forth in claim 1 wherein the otherwise empty spaces formed prior to installation of the cable, during the installation of the cable, and after the cable is placed in service, within said insulation layer and between said insulation layer and the conductor, contain the material which provides the cable with self sealing properties.
10. A method of making an insulated electriical cable which mitigates the effects of voids, punctures, or cracks formed in the insulation prior to installation of the cable, during the installation of the cable, and after the cable is placed in service comprising the steps of:
(a) forming a conductor;
(b) applying a layer of material which provides self sealing properties on the exterior of the conductor; and (c) forming an insulation layer around the conductor.
(a) forming a conductor;
(b) applying a layer of material which provides self sealing properties on the exterior of the conductor; and (c) forming an insulation layer around the conductor.
11. The method of claim 10 wherein the conductor is formed by a plurality of wires stranded together.
12. The method of claim 10 wherein said material is a dielectric.
13. The method of claim 12 wherein said material is flowable at about 25°C.
14. The method of claim 13 wherein said material has a 100 gram needle penetration value greater than 100 tenths of a millimeter at 25 °C.
15. The method of claim 14 wherein said material is a polymeric material.
16. The method of claim 15 wherein said material is an isomer.
17. The method of claim 16 wherein said material is a polyisobutene.
18. The method of claim 10 wherein said material flows into voids, punctures, or cracks in the insulation formed prior to the installation of the cable.
19. The method of claim 10 wherein said material flows into space between the conductor and the insulation formed prior to the installation of the cable.
20. The method of claim 10 wherein said material flows into space between the conductor and the insulation formed during the installation of the cable.
21. The method of claim 10 wherein said material flows into voids, punctures, or cracks in the insulation formed during the installation of the cable.
22. The method of claim 10 wherein said material flows into voids, punctures, or cracks in the insulation formed after the cable is placed in service.
23. The method of claim 10 wherein said material flows into space between the conductor and the insulation formed after the cable is placed in service.
24. The method of claim 10 including applying a water barner material over the conductor before applying the self-sealing material in step (b).
25. The method of claim 24 wherein the waoer barner is a polymer sheet.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/US2000/000703 WO2001052272A1 (en) | 1999-01-11 | 2000-01-12 | Electrical cable having a self-sealing agent and method for preventing water from contacting the conductor |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2332005A1 true CA2332005A1 (en) | 2001-07-12 |
Family
ID=21740966
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002332005A Abandoned CA2332005A1 (en) | 2000-01-12 | 2000-01-12 | Electrical cable having a self-sealing agent and method for preventing water from contacting the conductor |
Country Status (2)
| Country | Link |
|---|---|
| EP (1) | EP1190424A4 (en) |
| CA (1) | CA2332005A1 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN114141422A (en) * | 2020-09-03 | 2022-03-04 | 深圳市东佳信电线电缆有限公司 | Special structure environment-friendly power cable for transformer connection |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2973049B1 (en) | 2011-03-21 | 2016-12-23 | Arjowiggins Security | INFORMATION OR PAPER HOLDER HAVING A SELF-REPAIRING MATERIAL |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4095039A (en) * | 1976-04-16 | 1978-06-13 | General Cable Corporation | Power cable with improved filling compound |
| US4703132A (en) * | 1986-05-16 | 1987-10-27 | Pirelli Cable Corporation | Filling compound for multi-wire conductor of an electrical cable and cables including such compound |
| ATE254795T1 (en) * | 1998-03-04 | 2003-12-15 | Pirelli | ELECTRICAL CABLE WITH SELF-HEALING CABLE PROTECTION |
| US5983618A (en) * | 1998-03-31 | 1999-11-16 | Pirelli Cable Corporation | Apparatus, systems and methods for applying filling compound and water absorbing particles in a stranded conductor |
-
2000
- 2000-01-12 CA CA002332005A patent/CA2332005A1/en not_active Abandoned
- 2000-01-12 EP EP00908261A patent/EP1190424A4/en not_active Ceased
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN114141422A (en) * | 2020-09-03 | 2022-03-04 | 深圳市东佳信电线电缆有限公司 | Special structure environment-friendly power cable for transformer connection |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1190424A4 (en) | 2003-07-02 |
| EP1190424A1 (en) | 2002-03-27 |
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