US3055778A - Method for applying a mixture of a vinyl halide polymer and an epoxidized triglyceride on a wire and the resulting article - Google Patents
Method for applying a mixture of a vinyl halide polymer and an epoxidized triglyceride on a wire and the resulting article Download PDFInfo
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- US3055778A US3055778A US16936A US1693660A US3055778A US 3055778 A US3055778 A US 3055778A US 16936 A US16936 A US 16936A US 1693660 A US1693660 A US 1693660A US 3055778 A US3055778 A US 3055778A
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- United States
- Prior art keywords
- coating
- conductor
- vinyl halide
- wire
- zone
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Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B13/00—Apparatus or processes specially adapted for manufacturing conductors or cables
- H01B13/06—Insulating conductors or cables
- H01B13/14—Insulating conductors or cables by extrusion
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/022—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the choice of material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/03—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor characterised by the shape of the extruded material at extrusion
- B29C48/05—Filamentary, e.g. strands
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2101/00—Use of unspecified macromolecular compounds as moulding material
- B29K2101/10—Thermosetting resins
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2301/00—Use of unspecified macromolecular compounds as reinforcement
- B29K2301/10—Thermosetting resins
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
- Y10T428/294—Coated or with bond, impregnation or core including metal or compound thereof [excluding glass, ceramic and asbestos]
-
- 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31678—Of metal
- Y10T428/31692—Next to addition polymer from unsaturated monomers
- Y10T428/31699—Ester, halide or nitrile of addition polymer
Definitions
- the insulating compositions of this invention are fluid thermoplastic resins which remain fluid at extrusion temperatures but can be cured to a thermosetting form by a short-time, high-temperature treatment.
- These compositions comprise vinyl halide resins and oxirane containing fatty acyl derivatives such as epoxidized linseed oil, epoxidized safflower oil, epoxidized fish oils or epoxidized perilla oil wherein the unsaturation present in the fatty acyl radicals of the naturally occurring oil is substantially converted to oxirane groups providing a high oxirane triglyceride.
- the epoxidized oils are very low viscosity fluids having a residual iodine value of not more than 10.
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- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Mechanical Engineering (AREA)
- Organic Insulating Materials (AREA)
Description
Sept. 25, 1962 P H. RHODES METHOD FOR APPLYING A MIXTURE 'OF A VINYL HALIDE POLYMER AND AN EPOXIDIZED TRIGLYCERIDE ON A WIRE AND THE RESULTING ARTICLE Filed March 23, 1960 INVENTOR. PHIL-(PH. Elia-DEE ite This invention relates to the coating of metallic conductors with a plastic substance and to the coated conductor thereby produced. More particularly the invention relates to the extrusion coating of metallic cores with a heat hardenable thermosetting composition.
Various methods of manufacture have been employed in the past in the production of insulated metallic conductors, the diverse techniques for the most part being dictated by limitations inherent in the physical and chemical characteristics of the insulating material. In those cases where the nature of the insulating material permits, extrusion is a favored method for forming a sheath of the insulation around the core. Crosshead extrusion is a particularly desirable method since this technique provides a rapid and economic production means. Crosshead extrusion involves passing the wire conductor through a crosshead die and enveloping the conductor with the fluid coating composition followed by passage of the coated wire through a constricting die which presses the coating into close adherence with the conductor. Finally the coated conductor is passed to a cooling zone where the semifiuid coating is set.
Rubber compounds including mixtures of rubber compositions with resins such as polyethylene and vinyl halide resins have been employed in the insulation of wire in the past but such compositions possess shortcomings principal ly in high temperature resistance, chemical resistance, poor aging characteristics, low dielectric strength or poor flexibility. High temperature resistance is most important since the insulating composition is exposed to temperatures in excess of 400 F. in formulating and extruding and to much greater temperatures in actual use.
Moreover the insulated conductor should be capable of withstanding elevated temperatures Without flowing. The use of polyvinyl chloride resin compositions for this purpose has been restricted to comparatively low temperature use since such compositions tend to flow and break down with increasing temperature resulting in a decrease in dielectric properties. Utlimately as sufliciently high temperatures are reached the insulation flows away from the conductor causing shorts in the electrical system.
Thermosetting materials can be employed to avoid this high temperature softening or flow but thermosetting compositions do not provide the ease of handling of thermoplastics. Where thermosetting materials are employed as insulators extrusion cannot be employed as the coating technique since the temperatures required in the extruder for liquifying the resin cause a thermosetting material to set up in the extruder. The dip and draw method is employed for the application of thermosetting materials to conductors usually from a solution of the resin. Obviously only thin coatings can be applied by the dip and draw method as distinguished from the thicker coatings provided by extrusion.
It is therefore an object of this invention to provide an insulated filamentous electrical conductor having an improved resistance to flow at high temperatures.
A further object of the invention is the provision of a method for coating electrical conductors by extrusion of a thermoplastic composition on said conductor to provide an insulated conductor exhibiting desirable dielectric properties at high temperatures.
3,55,778 Patented Sept. 25, 1962 vide a coating having a greatly increased resistance to the effect of elevated temperatures. Inasmuch as the insulating composition is thermo lasticand thus fiowable at formulating and extrusion temperatures, yet does not set up at these temperatures, substantial benefits are provided in high production speeds and efficiency and uniformity of coating. Wide variations in size of the wire coated and thickness in coatings are possible. Additionall high temperature curing produces a tough yet fleidble'a'diie'r t' insulation possessing a greatly increased resistance to softening and flow when the cured coating is exposed to elevated z temperatures. Also the coating shows a greatly improved resistance to chemicals and solvents, has good impact strength, and good resistance to abrasion.
The FIGURE illustrates equipment which may be utilized in carrying out the method of the invention.
The insulating compositions of this invention are fluid thermoplastic resins which remain fluid at extrusion temperatures but can be cured to a thermosetting form by a short-time, high-temperature treatment. These compositions comprise vinyl halide resins and oxirane containing fatty acyl derivatives such as epoxidized linseed oil, epoxidized safflower oil, epoxidized fish oils or epoxidized perilla oil wherein the unsaturation present in the fatty acyl radicals of the naturally occurring oil is substantially converted to oxirane groups providing a high oxirane triglyceride. The epoxidized oils are very low viscosity fluids having a residual iodine value of not more than 10. The oxirane containing fatty acyl derivative must contain several three-membered epoxy groups in internal openchained portions of the molecule to provide an average epoxy content greater than about 8.5% and preferably about 8.89.5%. Esters of high oxirane fatty acids with lower mono-, di-, and polyhydric alcohols are particularly desirable. These esters are characterized as high oxirane fatty materials containing oxirane rings (epoxy groups) at those points in the fatty acyl radical which are normally occupied by double bonds in the original non-epoxidized fatty acid or ester. The di-, tri-, tetra-, penta-, and hexahydric alcohol esters of oxirane containing fatty acids of 1030 carbons containing more than 8.5% oxirane oxygen are preferred. Best results are obtained if these compositions have been subjected to alkali refining as is disclosed in copending application Serial Number 807,985, filed April 22, 1959, and also deodorized. Refining insures that by-products such as peroxides and hydroxyl groups are reduced to a minimum while deodorization removes volatiles which might cause gassing in the resin coating.
The vinyl halide resin component should contain a predominant portion, i.e., greater than 50% vinyl halide and lesser amounts of other monoolefinic monomers. This includes polymers prepared from 5'095% of vinyl halide units such as co-polymers and interpolymers of vinyl chloride with vinylidene chloride, vinyl esters, such as vinyl acetate, vinyl butyrate, and the like, and acrylic and alkylacrylic acid esters. Particularly preferred thermoplastic resins are those having 70-99% vinyl chloride units and smaller amounts, up to about 30% vinylidene chloride and vinyl esters. A preferred example is a thermoplastic resin containing 95% polyvinyl chloride units. Very suitable vinyl halide resins are the high molecular weight polyvinyl chloride resins having a molecular weight above about 20,000 and preferably around 100,000-200,000.
The preparation of the curable insulating composition involves techniques which are for the most part well known in the art. The thermoplastic resin may be dispersed in the epoxidized fatty material and the two components may be blended and compounded in a Banbury mixer or on a two-roll mill or other suitable compounding equip ment. Usually about 20-80 parts of the epoxide for each 100 parts of the resin will provide a desirable coating depending upon the flexibility and strength required for a given instance. A preferred example is 4080 parts based on the vinyl halide resin of epoxidized linseed oil. Fillers, stabilizers, pigments, and lubricants may also be incorporated in the mix. The components may first be mixed in the Banbury mixer for about minutes more or less at a temperature of around ZOO-300 F. followed by sheeting at about 240260 F. on a mill. The sheets may then be granulated and fed to an extruder which is heated at around 300-400 F. and then extruded on the core. It can be seen that the mix must be fluid and remain fluid when exposed to elevated temperatures during the handling time. Although setting up of the composition is not a problem with heat stable thermoplastic materials, such exposure to heat during handling and compounding obviously is not possible with thermosetting compositions.
The following examples which are intended to be illustrative only show the preparation of coated conductors and the physical characteristics thereof.
Example I A mixture of 100 parts of polyvinyl chloride resin (Geon-103) 1 and 40 parts of alkali refined, deodorized epoxidized linseed oil (oxirane content 9.02) containing 50 parts of satintone clay, 2 parts of pigment, and /2 part of zinc stearate lubricant is blended and compounded in a Banbury mixer at a temperature in the range 350-405 F. The mix is then sheeted on a two-roll mill and hot strip fed to an extruder directly from the two-roll mill. The heated screw type extruder is equipped with an appropriate crosshead wire coating die. The resin composition is liquefied by the heat of the extruder and the flowable resinous mixture enters the center of the die while the wire enters from one side of the die. The coated wire emerges from the opposite side of the die and is passed directly to a curing oven where the coated conductor is subjected to a high temperature (about 500-550 F.) and a treating time of approximately 2-20 seconds. The physical characteristics Similar results are obtained when epoxidized safflower oil, epoxidized perilla oil, or purified epoxidized fish oils are employed as the source of the fluid epoxide.
The coating from a similarly coated conductor having conventionally plasticized polyvinyl chloride as the coating possessed the following physical characteristics.
1. Tensile strength p.s.i 3200 2. Percent elongation 120 3. Trichloroethylene extraction (24 hrs. at 100 F.) percent 19.5 4. Soapy water extraction (24 hrs. at 100 F.) do 3.5 5. Tensile strength p.s.i. after aging 7 days at 100 In the drawing an unwind reel 10 contains the wire source 12 which which is fed into an extruder 11 which is equipped with a standard crosshead die. The resin coat- B. F. Goodrich & Co., Cleveland 15, Ohio.
' are particularly dsirable for this purpose.
subjected to high terrfieha ture to render the coating thermo setting. The wire having the hard protective coating is then passed through cooling bath 16 and wound around capstan 17. Rewind reel 18 is provided for use in preparing rolls of the coated conductor for storage and shipment.
The apparatus employed in the coating operations described herein comprises an NRM 1 /2 extruder with a standard wire coating crosshead. The die employed produces .030 insulation on an 18 gauge copper wire, the finished wire being .100 in diameter. Usually the thickness of the coating is about 60-100% of the thickness of the core. Following the extruder in the line is a tunnel type curing oven. The oven is constructed so as to provide temperatures up to about ll0O F. From the curing oven the cured coated conductor is conveyed through a cooling water tank and then wound on reels.
The curing temperature as in all curing cycles is adjusted to and dependent upon the time of exposure of the coating Within the curing zone. Increases in the rate of passage of the coated wire through the heat treating zone requires that the temperature of the zone be increased to insure that a cure will be realized in the shorter residence time within the zone. Correlation of curing temperatures with curing times to obtain a desired degree of cure is well within the ability of the skilled artisan. For the purpose of the present examples, cures are effected at 550 F. with an average residence time within the curing Zone of 2 seconds. Curing time can be accelerated by use of one of the conventional epoxy curing agents in the composition. Dibasic acids, polybasic acids and the anhydrides thereof Such known epoxy curing agents as isophthalic acid, Nadic anhydride, pyromellitic dianhydride, phthalic acid, terephthalic acid, phthalic anhydride, and trimellitic anhydride are particularly desirable for this purpose. Also the strong Lewis acids such as boron trifluoride and boron trifluoride complexes can be used.
Electrical conductors made in accordance with the method hereinbefore disclosed have significant physical and electrical advantages over conductors heretofore known. Since the coating exhibits good dielectric properties, a greater resistance to deterioration on aging, good flexibility, heat resistance, and abrasion resistance, it is adapted to a wide area of diverse uses. The coating exhibits excellent adherence to the core when cured, has good pigmenting properties and high impact strength. Important advantages in handling result from the face that the coating composition is fluid and easily handled without objectionable degradation at extrusion temperatures but cures easily to a tough, hard, heat and chemical resistant thermoset form.
Obviously many modifications and variations of the invention as hereinbefore set forth may be made Without departing from the spirit and scope thereof and therefore only such limitations are to be imposed as are indicated in the appended claims.
I claim:
1. An electrical conductor provided with a heat resistant tough adherent coating of high dielectric strength comprising: a filamentous metallic conductor continuously coated with a cured mixture of a polyvinyl halide polymer containing at least 50% vinyl halide units and an epoxidized triglyceride having an oxirane content in excess of 8.8%.
2. A method of coating an electrical conductor with a thermoplastic composition which may be rendered thermosetting by heat comprising: conveying a filamentous metal strip through an extrusion zone; enveloping said metal strip with a heated fluid mixture of a vinyl halide polymer containing at least 50% vinyl halide units and epoxidized triglyceride having an oxirane content in excess of 8.8%; continuously removing said coated conductor from said extruding zone; passing said conductor through a heat curing zone whereby to harden the coating of said polymer on said metal strip and increase the adherence of said coating to said metal strip and passing said coated conductor through a cooling zone.
3. A method of manufacturing an insulated conductor having an improved resistance to breakdown at high temperatures comprising: passing a filamentous metal conductor through an extrusion zone; continuously extruding a polymeric vinyl halide coating composition at a temperature above its fusion point around said conductor to form a sheath of the polymer around the conductor; passing the sheathed conductor through a constriction zone to compress said sheath around said conductor; passing said sheathed conductor through a curing zone maintained at a temperature above about 500 F. to effect curing of said sheath; and cooling said conductor with said insulation continuously coated thereon.
4. A method for manufacturing an insulated electrical conductor comprising: passing a filamentous metal core through an extrusion zone; extruding a thermoplastic polymer around said conductor, said polymer comprising a mixture of a vinyl halide resin containing at least 50% vinyl halide units and 40-80 parts based on said vinyl halide resin of epoxidized linseed oil having an oxirane content greater than 8.5% and an iodine value not greater than 10.
5. An insulated electrical conductor of improved flexibility and resistance to softening and flow upon exposure to elevated temperatures comprising: a filamentous metallic core continuously coated with a thermoplastic resin mixture of polyvinyl chloride and epoxidized linseed oil, said polyvinyl chloride containing 90-95% polyvinyl chloride units, said epoxidized linseed oil containing more than about 8.5% oxirane oxygen, the thickness of said coating being about 60100% of the thickness of said core.
6. An electrical conductor provided with a heat-resistant, tough, adherent coating of high dielectric strength comprising: a filamentous metallic conductor continuously coated with a cured mixture of a polyvinyl halide polymer containing at least 50% polymerized vinyl halide units and about -80 parts based on the weight of said polymer of an epoxidized triglyceride having an oxirane content in excess of 8.8%.
References Cited in the file of this patent UNITED STATES PATENTS 2,528,523 Kent Nov. 7, 1950 2,559,177 Terry et a1. July 3, 1951 2,569,502 Swern et al. Oct. 2, 1951 2,795,565 Newey June 11, 1957 2,810,733 Greenspan Oct. 22, 1957 2,836,605 Rowland et al. May 27, 1958 2,889,338 Dazzi June 2, 1959 FOREIGN PATENTS 762,856 Germany Mar. 23, 1953 512,026 Canada Apr. 19, 1955
Claims (1)
- 2. A METHOD OF COATING AN ELECTRIAL CONDUCTOR WITH A THEMOPLASTIC COMPOSITION WHICH MAY BE RENDERED THEMOSETTING BY HEAT COMPRISING: CONVERYING A FILAMENTOUS METAL STRIP THROUGH AN EXTRUSION ZONE; ENVELOPING SAID METAL STRIP WITH A HEATED FLUID MIXTURE OF A VINYL HALIDE POLYMER CONTAINING AT LEAST 50% VINYL HALIDE UNITS AND EPOXIDIZED TRIGLYCERIDE HAVING AN OXIRANE CONTENT IN EXCESS OF 8.8%; CONTINUOUSLY REMOVING SAID COATED CONDUCTOR FROM SAID EXTRUDING ZONE; PASSING SAID CONDUCTTOR THROUGH A HEAT CURING ZONE WHEREBY TO HARDEN THE COATING OF SAID POLYMER ON SAID MWTAL STRIP AND INCREASE THE ADHERENCE OF SAID COATING TO SAID METAL STRIP AND PASSING SAID COATED CONDUCTOR THROUGH A COOLING ZONE.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US16936A US3055778A (en) | 1960-03-23 | 1960-03-23 | Method for applying a mixture of a vinyl halide polymer and an epoxidized triglyceride on a wire and the resulting article |
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Application Number | Priority Date | Filing Date | Title |
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US16936A US3055778A (en) | 1960-03-23 | 1960-03-23 | Method for applying a mixture of a vinyl halide polymer and an epoxidized triglyceride on a wire and the resulting article |
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US3055778A true US3055778A (en) | 1962-09-25 |
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US16936A Expired - Lifetime US3055778A (en) | 1960-03-23 | 1960-03-23 | Method for applying a mixture of a vinyl halide polymer and an epoxidized triglyceride on a wire and the resulting article |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3283936A (en) * | 1962-11-02 | 1966-11-08 | Continental Can Co | Cured vinyl chloride resin-epoxidized linseed oil compositions as closure cap gaskets |
US3287297A (en) * | 1961-08-04 | 1966-11-22 | Consortium Elektrochem Ind | Coating compositions comprising vinyl chloride polymers and drying oil acid esters of liquid polyepoxides |
US4495312A (en) * | 1982-03-16 | 1985-01-22 | Sekisui Kagaku Kogyo Kabushiki Kaisha | Resin composition suitable for use in medical devices |
US4772435A (en) * | 1984-12-14 | 1988-09-20 | Maillefer S.A. | Method of sheathing a fiber optic |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2528523A (en) * | 1948-06-12 | 1950-11-07 | Du Pont | Process for extruding and insolubilizing polymers of ethylene |
US2559177A (en) * | 1950-05-01 | 1951-07-03 | Gen Mills Inc | Plasticized polyvinyl resin compositions |
US2569502A (en) * | 1945-02-07 | 1951-10-02 | Swern Daniel | Epoxidized oils |
DE762856C (en) * | 1940-02-21 | 1953-03-23 | Siemens Schuckertwerke A G | Method for covering electrical lines with a non-metallic cover |
CA512026A (en) * | 1955-04-19 | H. Chadbourne Joseph | Manufacture of thermo-plastic articles | |
US2795565A (en) * | 1953-11-09 | 1957-06-11 | Shell Dev | Method for preparing hard flexible vinyl halide polymer-liquid polyepoxide compositions and resulting products |
US2810733A (en) * | 1954-03-23 | 1957-10-22 | Fmc Corp | Peracid epoxidation of fatty acid esters |
US2836605A (en) * | 1958-05-27 | In situ epoxidatiqn using acetic anhy- | ||
US2889338A (en) * | 1955-07-28 | 1959-06-02 | Monsanto Chemicals | Epoxidized esters |
-
1960
- 1960-03-23 US US16936A patent/US3055778A/en not_active Expired - Lifetime
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA512026A (en) * | 1955-04-19 | H. Chadbourne Joseph | Manufacture of thermo-plastic articles | |
US2836605A (en) * | 1958-05-27 | In situ epoxidatiqn using acetic anhy- | ||
DE762856C (en) * | 1940-02-21 | 1953-03-23 | Siemens Schuckertwerke A G | Method for covering electrical lines with a non-metallic cover |
US2569502A (en) * | 1945-02-07 | 1951-10-02 | Swern Daniel | Epoxidized oils |
US2528523A (en) * | 1948-06-12 | 1950-11-07 | Du Pont | Process for extruding and insolubilizing polymers of ethylene |
US2559177A (en) * | 1950-05-01 | 1951-07-03 | Gen Mills Inc | Plasticized polyvinyl resin compositions |
US2795565A (en) * | 1953-11-09 | 1957-06-11 | Shell Dev | Method for preparing hard flexible vinyl halide polymer-liquid polyepoxide compositions and resulting products |
US2810733A (en) * | 1954-03-23 | 1957-10-22 | Fmc Corp | Peracid epoxidation of fatty acid esters |
US2889338A (en) * | 1955-07-28 | 1959-06-02 | Monsanto Chemicals | Epoxidized esters |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3287297A (en) * | 1961-08-04 | 1966-11-22 | Consortium Elektrochem Ind | Coating compositions comprising vinyl chloride polymers and drying oil acid esters of liquid polyepoxides |
US3283936A (en) * | 1962-11-02 | 1966-11-08 | Continental Can Co | Cured vinyl chloride resin-epoxidized linseed oil compositions as closure cap gaskets |
US4495312A (en) * | 1982-03-16 | 1985-01-22 | Sekisui Kagaku Kogyo Kabushiki Kaisha | Resin composition suitable for use in medical devices |
US4772435A (en) * | 1984-12-14 | 1988-09-20 | Maillefer S.A. | Method of sheathing a fiber optic |
US4893998A (en) * | 1984-12-14 | 1990-01-16 | Maillefer S.A. | Installation for producing a fiber optic cable component |
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