USH624H - Polybutylene gel filled cables - Google Patents
Polybutylene gel filled cables Download PDFInfo
- Publication number
- USH624H USH624H US07/017,120 US1712087A USH624H US H624 H USH624 H US H624H US 1712087 A US1712087 A US 1712087A US H624 H USH624 H US H624H
- Authority
- US
- United States
- Prior art keywords
- weight
- percent
- gel
- cable
- butene
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
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- -1 Polybutylene Polymers 0.000 title claims abstract description 14
- 229920001748 polybutylene Polymers 0.000 title abstract description 9
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims abstract description 38
- 239000003921 oil Substances 0.000 claims abstract description 17
- 229920000642 polymer Polymers 0.000 claims abstract description 17
- 229920001577 copolymer Polymers 0.000 claims abstract description 16
- 125000003118 aryl group Chemical group 0.000 claims abstract description 9
- 230000002441 reversible effect Effects 0.000 claims abstract description 7
- 239000010690 paraffinic oil Substances 0.000 claims abstract description 6
- 229920006132 styrene block copolymer Polymers 0.000 claims abstract description 6
- 150000001875 compounds Chemical class 0.000 claims description 9
- 239000005977 Ethylene Substances 0.000 abstract description 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract description 4
- 239000000499 gel Substances 0.000 description 40
- 239000000463 material Substances 0.000 description 26
- 239000008393 encapsulating agent Substances 0.000 description 15
- 238000002844 melting Methods 0.000 description 7
- 230000008018 melting Effects 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 239000012530 fluid Substances 0.000 description 4
- 229920001519 homopolymer Polymers 0.000 description 4
- 238000012423 maintenance Methods 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 230000002209 hydrophobic effect Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 230000005540 biological transmission Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 235000019271 petrolatum Nutrition 0.000 description 2
- 239000010734 process oil Substances 0.000 description 2
- 239000005060 rubber Substances 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- RLRINNKRRPQIGW-UHFFFAOYSA-N 1-ethenyl-2-[4-(2-ethenylphenyl)butyl]benzene Chemical compound C=CC1=CC=CC=C1CCCCC1=CC=CC=C1C=C RLRINNKRRPQIGW-UHFFFAOYSA-N 0.000 description 1
- 229920002633 Kraton (polymer) Polymers 0.000 description 1
- 239000010692 aromatic oil Substances 0.000 description 1
- 229920005601 base polymer Polymers 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005429 filling process Methods 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229920005996 polystyrene-poly(ethylene-butylene)-polystyrene Polymers 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000003303 reheating Methods 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
Images
Classifications
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- 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
- H01B3/20—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances liquids, e.g. oils
- H01B3/22—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances liquids, e.g. oils hydrocarbons
-
- 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
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B7/00—Insulated conductors or cables characterised by their form
- H01B7/17—Protection against damage caused by external factors, e.g. sheaths or armouring
- H01B7/28—Protection against damage caused by moisture, corrosion, chemical attack or weather
- H01B7/282—Preventing penetration of fluid, e.g. water or humidity, into conductor or cable
- H01B7/285—Preventing penetration of fluid, e.g. water or humidity, into conductor or cable by completely or partially filling interstices in the cable
-
- 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
Definitions
- the solution that has been widely adopted is to fill the voids in the cable with a water insoluble filling material that simply encapsulates the cable components to prevent water intrusion.
- a water insoluble filling material that simply encapsulates the cable components to prevent water intrusion.
- this physical function of the cable filling material is straight-forward, the choice of the material is not.
- the hydrophobic nature of the material low temperature properties, flow characteristics at elevated temperatures, the highest temperature at which the encapsulant may be used (“upper service temperature"), processing characteristics, handling characteristics, dielectric properties, toxicity and cost.
- U.S. Pat. No. 4,259,540 discloses the use of a sytrene-ethylene butylene-styrene block copolymer, polyethylene, and a paraffinic or napthenic oil, where the oil has a maximum of 5% aromatic oils, in order to enable the cable encapsulant to meet the functional requirements of the cable and to provide good handling characteristics that the petroleum jelly material does not possess.
- Previously used encapsulants required that it and the cable be heated to a temperature well above the melting point of the encapsulant (i.e., the upper service temperature) in order to significantly reduce the viscosity of the fluid to allow filling of the cable.
- This heating is energy intensive and may be damaging to some of the electrical components of the cables. It also precludes the use of desirable cable component materials that may be advantageous, but which cannot tolerate high filling temperatures of these encapsulants.
- an encapsulant which is thermally reversible has long been sought. This means that the encapsulant may be removed and replaced during maintenance time and time again at a temperature below the temperature that would damage the cables.
- An encapsulant which is thermally reversible can be heated to a liquid and then cooled to a gel over and over again without damage to the nature of the filling material, or cable components. This is especially true in hydrophone cables that are generally not permanently installed but towed at sea where the utility of such invention is paramount.
- This invention includes a slow forming, thermally reversible gel so that it may be heated to a liquid and cooled to a gel over and over again at a temperature below the temperature that will damage the cables so that the gel may be removed and replaced during maintenance.
- the gel is slow forming, as the viscosity of the clear liquid rises over a period of several hours to several days to form the gel. It is this length of time that one has to fill the cables before the gel material becomes too viscous to flow, or remove the gel during maintenance.
- the gel is based on light hydrocarbon process oils and isotactic butene-1 polymers or butene-1 copolymers.
- the filling material or gel encapsulating compound comprises from about 2 percent by weight to about 8 percent by weight butene-1 polymer or copolymer, wherein said butene-1 polymer or copolymer contains from about 0 percent by weight to about 10 percent by weight of a C 2 -C 5 comonomer and from about 0 percent by weight to about 10 percent by weight of a styrene-ethylene-butylene styrene block copolymer, and from about 82 percent by weight to about 98 percent by weight of a naphthenic or paraffinic oil with an aromatic content of up to 25 percent by weight.
- the encapsulating compound is preferably about 6 percent by weight butene-1 polymer or copolymer wherein the butene-1 polymer or copolymer contains preferably about 6 percent by weight comonomer, preferably about 5% by weight of the S-EB-S block copolymer, and preferably about 89 percent by weight of a naphthenic or paraffinic oil with an aromatic content of preferably about 15 percent by weight.
- the C 2 -C 5 comonomer is preferably an ethylenic comonomer.
- This invention also includes a cable or other conduit requiring water protection which contains the encapsulating compound described above.
- FIG. 1 is a graph which compares the polybutylene gel upper service temperature and the temperatures at which previously described encapsulants such as waxes, rubbers, etc. had to be filled, as well as the temperature at which the encapsulating gel compound of the present invention may be filled.
- the encapsulating compound or gel of the present invention has the following properties:
- the material Above the gel temperature the material is a clear, low viscosity fluid
- the gel is thermally reversible at a temperature below the temperature that will damage the cables so that the gel may be removed and replaced during maintenance.
- the melting temperature, forming temperature, and forming time of the gel can be controlled by the choice and concentration of the polybutylene polymeric component by copolymerization or homopolymer in the base polymer.
- the gel is hydrophobic and protects the cable from water leakage.
- the gel is based on light hydrocarbon process oils and isotactic butene-1 polymer or butene-1 copolymers. Because of their compatibility with the oils and crystallinity, the isotactic butene-1 polymers or copolymers dissolve in the oils above the polymers' melting temperature. Once dissolved, these polymers exhibit very slow recrystallization and gel network formation from solution as the temperature is lowered allowing the material to remain fluid at temperatures much below the gel's melting temperature for a period of approximately 24 to 48 hours. Eventually, the polymeric polybutylene crystallites form and become connected in a network forming a translucent gel.
- the ethylenic comonomer containing polybutene-1 gel of Example 2 is filled into a suitable cable within 24-48 hours after initial cooling from the solution.
- the cable is ready for use within approximately 12 hours after such filling.
- a comonomer which may be a C 2 -C 5 comonomer and in the range of 2 to 8 percent, but preferably about 6 percent ethylene comonomer, has a dramatic effect on the properties of the gel.
- hydrocarbon fluids above the molecular weight of 150 will be gelled by isotactic butene-1 homopolymers and copolymers.
- HVI 100 N oil has been used which has a 16 percent aromatic content.
- Shellflex® 131 which may be obtained from Shell Oil Company, Houston, Tex. may also be used as a suitable oil which contains about 24 percent aromatic content as well as Sunpar® 120 LW available from Sun Oil Co. contains less than 5 percent aromatic content.
- blends of polybutylene with microcrystalline waxes such as Shellmax 500, available from Shell Oil Company, Houston, Tex. produced a firmer, more opaque gel which forms somewhat more rapidly than that gel claimed by applicants.
- the encapsulating or gel of applicant's invention is filled at 55° to 60° C. --well below the polybutene-1 use temperature of 80° C.
- the firm gel forming temperature is at 30° C. and the filling range is thus a 50° C. range between 80° C. and 30° C.
- a filling material of waxes or rubbers were used, such filling material would have to be filled, as indicated in FIG. 1, at a point above the 80° C. use temperature of the polybutene-1. This would necessitate, of course, a time consuming and cost inefficient additional heating step prior to filling, as well as a reheating every time it became necessary to refill the cable because of leaks or other problems.
- the use of such materials would also preclude the use of cable components sensitive to temperatures above 80° C.
- Applicant's invention encompasses a gel material which is not only slow forming to allow plenty of time to fill the cable without an additional heating step, but is also thermally reversible so that if the cable is later punctured and the gel material must be released and/or refilled into the cable, it may be heated to solution and cooled to the filling temperature over and over again without any loss of the gel materials' desirable filling characteristics.
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- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Insulated Conductors (AREA)
Abstract
A slow forming, thermally reversible gel for filling cables at or below the polybutylene use temperature, which comprises a butene-1 polymer or copolymer which may contain either or both ethylene comonomer and a styrene-ethylene-butylene-styrene block copolymer, and the rest naphthenic or paraffinic oil with an oil aromatic content up to 25% by weight.
Description
This is a division of application Ser. No. 679,169, filed Dec. 6, 1984.
Cables for power, electronic (telephone) transmission, hydrophone cables for oil exploration at sea and other various uses have been filled with various substances in order to protect against water intrusion since 1970. Intrusion occurs when water penetrates into a localized opening in a cable sheath and is free to channel as far as physical processes for water spread and transport allow, often hundreds of feet. Not only does this upset capacitance balance of the transmission cable line but it introduces more potential corrosion sites in proproportion to the length of wire that is wetted. The useful life of water-soaked wires is obviously shorter than that of dry wires.
The solution that has been widely adopted is to fill the voids in the cable with a water insoluble filling material that simply encapsulates the cable components to prevent water intrusion. However, although this physical function of the cable filling material is straight-forward, the choice of the material is not. Among the many considerations that are important for materials used in this application are the hydrophobic nature of the material, low temperature properties, flow characteristics at elevated temperatures, the highest temperature at which the encapsulant may be used ("upper service temperature"), processing characteristics, handling characteristics, dielectric properties, toxicity and cost.
Materials that satisfy most of these criteria and which have been widely used are described in U.S. Pat. Nos. 3,607,487 and 3,717,716 issued Sept. 21, 1971 and Feb. 20, 1973 respectively. These materials are essentially a petroleum jelly, mixed with a polymer, usually polyethylene, to impart consistency and prevent flowing at warm temperatures below the upper service temperature.
Similar hydrophobic encapsulants have been proposed for filling splice closures. For example, U.S. Pat. No. 3,879,575 issued Apr. 22, 1975 describes a mixture of a low viscosity oil gelled by a styrene-isoprene-styrene copolymer, again with polyethylene added to impart consistency and reduce slump.
U.S. Pat. No. 4,259,540 discloses the use of a sytrene-ethylene butylene-styrene block copolymer, polyethylene, and a paraffinic or napthenic oil, where the oil has a maximum of 5% aromatic oils, in order to enable the cable encapsulant to meet the functional requirements of the cable and to provide good handling characteristics that the petroleum jelly material does not possess.
However, all of these above-described encapsulants during the filling process, must be heated to a temperature above the "upper service temperature" of the encapsulant. The upper service temperature of the material is the temperature above which the material cannot be used in the cable. Thus, filling of most materials requires a time consuming step in order to heat the encapsulant to a pumpable consistency for filling. There has been long felt need for an encapsulant which meets other filling material requirements but which could be processed into the cable well below the "upper service temperature" of the encapsulant. Previously used encapsulants required that it and the cable be heated to a temperature well above the melting point of the encapsulant (i.e., the upper service temperature) in order to significantly reduce the viscosity of the fluid to allow filling of the cable. This heating is energy intensive and may be damaging to some of the electrical components of the cables. It also precludes the use of desirable cable component materials that may be advantageous, but which cannot tolerate high filling temperatures of these encapsulants.
In addition, an encapsulant which is thermally reversible has long been sought. This means that the encapsulant may be removed and replaced during maintenance time and time again at a temperature below the temperature that would damage the cables. An encapsulant which is thermally reversible can be heated to a liquid and then cooled to a gel over and over again without damage to the nature of the filling material, or cable components. This is especially true in hydrophone cables that are generally not permanently installed but towed at sea where the utility of such invention is paramount.
This invention includes a slow forming, thermally reversible gel so that it may be heated to a liquid and cooled to a gel over and over again at a temperature below the temperature that will damage the cables so that the gel may be removed and replaced during maintenance. The gel is slow forming, as the viscosity of the clear liquid rises over a period of several hours to several days to form the gel. It is this length of time that one has to fill the cables before the gel material becomes too viscous to flow, or remove the gel during maintenance.
The gel is based on light hydrocarbon process oils and isotactic butene-1 polymers or butene-1 copolymers. The filling material or gel encapsulating compound comprises from about 2 percent by weight to about 8 percent by weight butene-1 polymer or copolymer, wherein said butene-1 polymer or copolymer contains from about 0 percent by weight to about 10 percent by weight of a C2 -C5 comonomer and from about 0 percent by weight to about 10 percent by weight of a styrene-ethylene-butylene styrene block copolymer, and from about 82 percent by weight to about 98 percent by weight of a naphthenic or paraffinic oil with an aromatic content of up to 25 percent by weight. The encapsulating compound is preferably about 6 percent by weight butene-1 polymer or copolymer wherein the butene-1 polymer or copolymer contains preferably about 6 percent by weight comonomer, preferably about 5% by weight of the S-EB-S block copolymer, and preferably about 89 percent by weight of a naphthenic or paraffinic oil with an aromatic content of preferably about 15 percent by weight. The C2 -C5 comonomer is preferably an ethylenic comonomer.
This invention also includes a cable or other conduit requiring water protection which contains the encapsulating compound described above.
FIG. 1 is a graph which compares the polybutylene gel upper service temperature and the temperatures at which previously described encapsulants such as waxes, rubbers, etc. had to be filled, as well as the temperature at which the encapsulating gel compound of the present invention may be filled.
The encapsulating compound or gel of the present invention has the following properties:
(1) Above the gel temperature the material is a clear, low viscosity fluid;
(2) after cooling to room temperature the viscosity rises over a period of several hours to several days to form a gel, rendering the material too viscous to flow.
(3) As the gel forms it becomes translucent.
(4) The gel is thermally reversible at a temperature below the temperature that will damage the cables so that the gel may be removed and replaced during maintenance.
(5) The melting temperature, forming temperature, and forming time of the gel can be controlled by the choice and concentration of the polybutylene polymeric component by copolymerization or homopolymer in the base polymer.
(6) The gel is hydrophobic and protects the cable from water leakage.
The gel is based on light hydrocarbon process oils and isotactic butene-1 polymer or butene-1 copolymers. Because of their compatibility with the oils and crystallinity, the isotactic butene-1 polymers or copolymers dissolve in the oils above the polymers' melting temperature. Once dissolved, these polymers exhibit very slow recrystallization and gel network formation from solution as the temperature is lowered allowing the material to remain fluid at temperatures much below the gel's melting temperature for a period of approximately 24 to 48 hours. Eventually, the polymeric polybutylene crystallites form and become connected in a network forming a translucent gel.
Applicants have found that the presence of ethylene comonomer decreases both the gel's melting temperature and a rate of crystallization.
An isotactic butene-1 homopolymer was dissolved in HVI 100 N oil at 120° C. so that the solution contained 6 percent isotactic butene-1 homopolymer. As the solution temperature was lowered the viscosity began to rise sharply at about 40° C. (taken as the minimum filling temperature) and continued to rise to form a firm gel within one hour of reaching room temperature. The gel formed had a melting point of about 80° C.
Six percent DP8010 isotactic butene-1 with 5.7 percent by weight ethylene comonomer was dissolved in HVI 100 N oil. The solution was cooled from 120° C., the temperature necessary for the dissolving, and the viscosity began to rise at about 30° C. The solution material formed into a viscous, usable gel within 24-48 hours after the intiation of the cooling process. The resulting gel had a melting point of 55°-60° C.
The ethylenic comonomer containing polybutene-1 gel of Example 2 is filled into a suitable cable within 24-48 hours after initial cooling from the solution. The cable is ready for use within approximately 12 hours after such filling.
It is apparent that the addition of a comonomer which may be a C2 -C5 comonomer and in the range of 2 to 8 percent, but preferably about 6 percent ethylene comonomer, has a dramatic effect on the properties of the gel. In addition, it is thought that many hydrocarbon fluids above the molecular weight of 150 will be gelled by isotactic butene-1 homopolymers and copolymers. For example, HVI 100 N oil has been used which has a 16 percent aromatic content. Shellflex® 131, which may be obtained from Shell Oil Company, Houston, Tex. may also be used as a suitable oil which contains about 24 percent aromatic content as well as Sunpar® 120 LW available from Sun Oil Co. contains less than 5 percent aromatic content.
It is also noted that blends of polybutylene with microcrystalline waxes such as Shellmax 500, available from Shell Oil Company, Houston, Tex. produced a firmer, more opaque gel which forms somewhat more rapidly than that gel claimed by applicants.
In addition, the addition of from about 0 percent by weight to about 10 percent by weight of KRATON® G thermoplastic rubbers, available from Shell Oil Company, Houston, Tex. increases the strength and clarity of the gels, with a slight decrease in gel formation time.
In reference to FIG. 1, it may be seen that the encapsulating or gel of applicant's invention is filled at 55° to 60° C. --well below the polybutene-1 use temperature of 80° C. The firm gel forming temperature is at 30° C. and the filling range is thus a 50° C. range between 80° C. and 30° C. If a filling material of waxes or rubbers were used, such filling material would have to be filled, as indicated in FIG. 1, at a point above the 80° C. use temperature of the polybutene-1. This would necessitate, of course, a time consuming and cost inefficient additional heating step prior to filling, as well as a reheating every time it became necessary to refill the cable because of leaks or other problems. The use of such materials would also preclude the use of cable components sensitive to temperatures above 80° C.
Applicant's invention encompasses a gel material which is not only slow forming to allow plenty of time to fill the cable without an additional heating step, but is also thermally reversible so that if the cable is later punctured and the gel material must be released and/or refilled into the cable, it may be heated to solution and cooled to the filling temperature over and over again without any loss of the gel materials' desirable filling characteristics.
Various additional modifications and extensions of this invention such as to various types of cable or not even to cable at all, will become apparent to those skilled in the art. All such variations and deviations which basically rely on the teachings through which this invention has advanced the art are properly considered to be within the spirit and scope of this invention.
Claims (4)
1. A cable which may be used for low temperature filling without sacrificing the use temperature, and which may be easily repaired, which comprises:
a cable body, which contains a slow forming, thermally reversible translucent encapsulating compound, wherein said encapsulating compound contains from about 2 percent by weight to about 8 percent by weight butene-1 polymer or copolymer, wherein said butene-1 polymer or copolymer contains from about 3 percent by weight to about 10 percent by weight of a C2 -C5 comonomer, and from about 92 percent by weight to about 95 percent by weight of a naphthenic or paraffinic oil, wherein said oil has an aromatic content of from about 5 percent by weight to about 25 percent by weight.
2. The cable of claim 1, which contains from about 0% by weight to about 10% by weight of styrene-ethylene-butylene-styrene block copolymer.
3. The cable of claim 1, wherein said translucent encapsulating compound consists of from about 4 percent by weight to about 7 percent by weihgt butene-1 polymer or copolymer, and wherein said butene-1 polymer or copolymer contains from about 3 percent by weight to about 8 percent by weight of said C2 -C5 comonomer, from about 4% by weight to about 6% by weight of a styrene-ethylene-butylene-styrene block copolymer, and from about 87 percent by weight to about 92 percent by weight of said naphthenic or paraffinic oil, wherein said oil has an aromatic content of from about 5 percent by weight to about 25 percent by weight.
4. The cable in claim 1, wherein said translucent encapsulating compound comprises preferably about 6 percent by weight butene-1 polymer or copolymer, and wherein said butene-1 polymer or copolymer contains preferably about 6 percent by weight of a C2 -C5 comonomer, preferably about 5% by weight of said styrene-ethylene-butylene-styrene block copolymer, and preferably about 89 percent by weight of said naphthenic or paraffinic oil, where said oil has an aromatic content of about 15 percent by weight.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/017,120 USH624H (en) | 1984-12-06 | 1987-02-20 | Polybutylene gel filled cables |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US67916984A | 1984-12-06 | 1984-12-06 | |
| US07/017,120 USH624H (en) | 1984-12-06 | 1987-02-20 | Polybutylene gel filled cables |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US67916984A Division | 1984-12-06 | 1984-12-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USH624H true USH624H (en) | 1989-04-04 |
Family
ID=26689481
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/017,120 Abandoned USH624H (en) | 1984-12-06 | 1987-02-20 | Polybutylene gel filled cables |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | USH624H (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0529957A1 (en) * | 1991-08-23 | 1993-03-03 | The Whitaker Corporation | Sealed electrical connectors |
| US5218011A (en) * | 1986-03-26 | 1993-06-08 | Waterguard Industries, Inc. | Composition for protecting the contents of an enclosed space from damage by invasive water |
| US5256705A (en) * | 1986-03-26 | 1993-10-26 | Waterguard Industries, Inc. | Composition with tackifier for protecting communication wires |
| US6253012B1 (en) | 1998-11-12 | 2001-06-26 | Alcatel | Cycled fiber lock for cross-functional totally dry optical fiber loose tube cable |
Citations (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU135943B2 (en) | 1947-04-28 | 1947-05-29 | British Insulated Callender's Cables Limited | An improved electrical insulating compound |
| US3607487A (en) | 1968-12-02 | 1971-09-21 | Bell Telephone Labor Inc | Waterproof electrical cable |
| US3684760A (en) | 1969-07-31 | 1972-08-15 | Huels Chemische Werke Ag | Molding compositions of polybutene-1 |
| US3717716A (en) | 1968-12-02 | 1973-02-20 | Bell Telephone Labor Inc | Plastic insulated conductor communications cable waterproofed with an internal void-filling mixture of petroleum jelly and high molecular weight polyethylene or polypropylene |
| US3775548A (en) | 1972-02-24 | 1973-11-27 | Essex International Inc | Filled telephone cable |
| DE2320254A1 (en) | 1973-04-19 | 1974-11-07 | Siemens Ag | Water-repellent filler for cable-fittings - contg paraffin oil, polybutene, polyethylene wax and colloidal silica |
| US3879575A (en) | 1974-02-21 | 1975-04-22 | Bell Telephone Labor Inc | Encapsulating compound and closure |
| US3893962A (en) | 1974-01-07 | 1975-07-08 | Basil Vivian Edwin Walton | Telephone cable filling composition (II) |
| US3915914A (en) | 1970-09-04 | 1975-10-28 | Huels Chemische Werke Ag | Asphalt compositions containing poly-1-butene and methods for preparing |
| DE1465676C3 (en) | 1964-06-03 | 1975-11-27 | Kabel- Und Metallwerke Gutehoffnungshuette Ag, 3000 Hannover | Filling compound for cable sleeves |
| US4140570A (en) | 1973-11-19 | 1979-02-20 | Texas Instruments Incorporated | Method of growing single crystal silicon by the Czochralski method which eliminates the need for post growth annealing for resistivity stabilization |
| US4259540A (en) | 1978-05-30 | 1981-03-31 | Bell Telephone Laboratories, Incorporated | Filled cables |
| US4324453A (en) | 1981-02-19 | 1982-04-13 | Siecor Corporation | Filling materials for electrical and light waveguide communications cables |
| US4351913A (en) | 1981-02-19 | 1982-09-28 | Siecor Corporation | Filling materials for electrical and light waveguide communications cables |
| US4361508A (en) | 1980-10-20 | 1982-11-30 | Arco Polymers, Inc. | Cable filler compositions comprising a mixture of (a) styrene block copolymer, (b) crystalline polypropylene copolymer and (c) mineral oil |
| US4361507A (en) | 1980-10-20 | 1982-11-30 | Arco Polymers, Inc. | Cable filler composition containing (a) crystalline polypropylene homopolymer, (b) styrene block copolymer and (c) mineral oil |
| GB2092176B (en) | 1981-01-30 | 1985-01-09 | Bicc Ltd | Compositions for use in electric cables |
| US4509821A (en) | 1981-09-10 | 1985-04-09 | Sun Tech, Inc. | Filling material for electric cable |
| US4617422A (en) | 1981-01-30 | 1986-10-14 | Bicc Public Limited Company | Electric cables and compositions for use in them |
-
1987
- 1987-02-20 US US07/017,120 patent/USH624H/en not_active Abandoned
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| AU135943B2 (en) | 1947-04-28 | 1947-05-29 | British Insulated Callender's Cables Limited | An improved electrical insulating compound |
| DE1465676C3 (en) | 1964-06-03 | 1975-11-27 | Kabel- Und Metallwerke Gutehoffnungshuette Ag, 3000 Hannover | Filling compound for cable sleeves |
| US3607487A (en) | 1968-12-02 | 1971-09-21 | Bell Telephone Labor Inc | Waterproof electrical cable |
| US3717716A (en) | 1968-12-02 | 1973-02-20 | Bell Telephone Labor Inc | Plastic insulated conductor communications cable waterproofed with an internal void-filling mixture of petroleum jelly and high molecular weight polyethylene or polypropylene |
| US3684760A (en) | 1969-07-31 | 1972-08-15 | Huels Chemische Werke Ag | Molding compositions of polybutene-1 |
| US3915914A (en) | 1970-09-04 | 1975-10-28 | Huels Chemische Werke Ag | Asphalt compositions containing poly-1-butene and methods for preparing |
| US3775548A (en) | 1972-02-24 | 1973-11-27 | Essex International Inc | Filled telephone cable |
| DE2320254A1 (en) | 1973-04-19 | 1974-11-07 | Siemens Ag | Water-repellent filler for cable-fittings - contg paraffin oil, polybutene, polyethylene wax and colloidal silica |
| US4140570A (en) | 1973-11-19 | 1979-02-20 | Texas Instruments Incorporated | Method of growing single crystal silicon by the Czochralski method which eliminates the need for post growth annealing for resistivity stabilization |
| US3893962A (en) | 1974-01-07 | 1975-07-08 | Basil Vivian Edwin Walton | Telephone cable filling composition (II) |
| US3879575A (en) | 1974-02-21 | 1975-04-22 | Bell Telephone Labor Inc | Encapsulating compound and closure |
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| US4361507A (en) | 1980-10-20 | 1982-11-30 | Arco Polymers, Inc. | Cable filler composition containing (a) crystalline polypropylene homopolymer, (b) styrene block copolymer and (c) mineral oil |
| GB2092176B (en) | 1981-01-30 | 1985-01-09 | Bicc Ltd | Compositions for use in electric cables |
| AU548825B2 (en) | 1981-01-30 | 1986-01-02 | Corning Communications Limited | Electric cables and compositions for use in them |
| US4617422A (en) | 1981-01-30 | 1986-10-14 | Bicc Public Limited Company | Electric cables and compositions for use in them |
| US4324453A (en) | 1981-02-19 | 1982-04-13 | Siecor Corporation | Filling materials for electrical and light waveguide communications cables |
| US4351913A (en) | 1981-02-19 | 1982-09-28 | Siecor Corporation | Filling materials for electrical and light waveguide communications cables |
| US4509821A (en) | 1981-09-10 | 1985-04-09 | Sun Tech, Inc. | Filling material for electric cable |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5218011A (en) * | 1986-03-26 | 1993-06-08 | Waterguard Industries, Inc. | Composition for protecting the contents of an enclosed space from damage by invasive water |
| US5256705A (en) * | 1986-03-26 | 1993-10-26 | Waterguard Industries, Inc. | Composition with tackifier for protecting communication wires |
| EP0529957A1 (en) * | 1991-08-23 | 1993-03-03 | The Whitaker Corporation | Sealed electrical connectors |
| EP0708454A3 (en) * | 1991-08-23 | 1996-08-28 | Whitaker Corp | Waterproof electrical connector |
| US6253012B1 (en) | 1998-11-12 | 2001-06-26 | Alcatel | Cycled fiber lock for cross-functional totally dry optical fiber loose tube cable |
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