US2437708A - Semiconducting tape for electric cable - Google Patents

Semiconducting tape for electric cable Download PDF

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US2437708A
US2437708A US522980A US52298044A US2437708A US 2437708 A US2437708 A US 2437708A US 522980 A US522980 A US 522980A US 52298044 A US52298044 A US 52298044A US 2437708 A US2437708 A US 2437708A
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polyamide
conducting
polyamides
tape
semi
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US522980A
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Plass Curtis Edward
Sullivan David Joseph
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American Steel and Wire Company of New Jersey
EIDP Inc
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American Steel and Wire Company of New Jersey
EI Du Pont de Nemours and Co
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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B9/00Power cables
    • H01B9/02Power cables with screens or conductive layers, e.g. for avoiding large potential gradients
    • H01B9/027Power cables with screens or conductive layers, e.g. for avoiding large potential gradients composed of semi-conducting layers

Definitions

  • This invention relates to a semi-conducting oil impervious coating material for use as an electrostatic shield on high tension insulated electrical conductors where it is desirable to maintain the voltage gradient at the surface of the insulation below a value above which harmful electrical disturbances occur.
  • polyamides are those which are soluble in a lower aliphatic monohydric alcohol, such as those disclosed in U. S. Patent 2,285,009 to Brubaker et al., granted June 2, 1942, and N-alkoxymethyl polyamides disclosed in Cairns application Ser. No. 445,635, filed June 3, 1942 (now abandoned).
  • the latter are a new class of nitrogen-substituted polyamides formed by reacting with an aldehyde and a formaldehyde-reactive organic compound having a hydrogen attached to an element of groups V and VI of series 2 and 3 of the periodic table, in the presence of an oxygencontaining acid catalyst, polyamides of the general type described in U. S. Patents 2,071,250, 2,071,253 and 2,130,948.
  • the polyamides of this kind generally speaking, comprise the reaction product of a linear polymer-forming composition containing amide-forming groups, for example, reacting material consisting essentially of bifunctional molecules each containing two reactive groups which are complementary to reactive groups in other molecules and which include complementary amide-forming groups.
  • polyamides can be obtained by the methods given in the above mentioned patents and by other methods, for example, by self-polymerization of a mono-aminomonocarboxylic acid, by reacting a diamine with a dibasic carboxylic acid in substantially equimolecular amounts, or by reacting a monoaminomonohydric alcohol with a dibasic carboxylic acid in substantially equimolecular amounts, it being understood that reference herein to the amino acids, diamines, dibasic carboxylic acids, and amino alcohols is intended to include the equivalent amide-forming derivatives of these reactants.
  • the preferred polyamides obtained from these reactants have a unit length of at least 7, where unit length is defined as in United States Patents 2,071,253 and 2,130,948.
  • the average number of carbon atoms separating the amide groups in these polyamides is at least two.
  • linear polyamides include also polymers, as for instance the polyester-amides, obtained by admixture of other linear polymer-forming reactants, as for instance glycol-dibasic acid mixtures or hydroxy acids, with the mentioned polyamide-forming reactants.
  • Both the simple and modified linear polyamides contain the recurring amide groups in which X is oxygen or sulfur and R is hydrogen or a monovalent hydrocarbon radical. as an integral part of the main chain of atoms in the polymer.
  • amino acid polymers yield the amino acid hydrochloride
  • diamine-dibasic acid polymers yield the diamine hydrochloride and the dibasic carboxylic acid
  • amino alcoholdibasic acid polymers yield the amino alcohol hydrochloride and the dibasic carboxylic acid
  • N-methoxymethyl polyhexamethylene adipamide which was prepared as follows:
  • the carbon black which is used may be prepared according to an article published in "Canadian Chemistry 8: Metallurgy, May, 1933,
  • FIGs 1 and 3 are diagrammatic partial sections of a high tension cable prepared according to the present invention.
  • Figure 4 is a diagrammatic section or a piece of semi-conducting tape.
  • I represents a conductor which may be solid or made up of a bundle of wires as shown.
  • an oiled paper layer 2 surrounds the conductor l. Over this oiled paper layer is applied a semi-conducting tape made up of a base 3 which may be paper 3 as shown in Figure 1, or the paper may be replaced by a suitable fabric.
  • the tape with the paper or fabric base is provided with a semi-conducting coating 5,
  • the tape is prepared by impregnating or-coating the base with a semi-conducting composition and cut into strips of suitable width, which is then wound around the insulated cable.
  • Figure 2 is a, modification of Figure 1 showing a rubber insulation 4 next to the conductor l instead of the oiled paper shown in Figure 1.
  • the semi-conducting tape also differs from Figure 1 in the cloth base 1 instead of the paper base 3.
  • the semi-conducting coating is covered with a conventional braid 6.
  • Figure 3 represents a modification of Figures 1 and 2 in which the semi-conducting tape is applied directly to the copper conductor I.
  • An insulation 8 is provided over the semi-conducting coating 5.
  • This insulation may be rubber shown as 4 in Figure 2 or oiled paper shown as 2 in Figure 1 or other types of electrical insulation.
  • Figure 4 illustrates a section of the semi-conducting tape which has a cloth base 1 and a semi-conducting co'ating 5, the composition of which will be more fully described in the following examples.
  • the resistance of the tape or unsupported layer should be of the order of300 to 1000 Ohms per inch square. may have a resistance of up to 2000 ohms or even more.
  • a cloth base it is preferable to' coat the same with about 2 to 4 ounces per square yard of polyamide-carbon black com-position.
  • a paper base about 1 ounce per square .yard is satisfactory.
  • the composition applied to the fabric or paper base may be prepared in any known manner or by methods illustrated by the following examples.
  • Example I The following ingredients were heated to about F. with stirring for 12 hours in a suitable mixer, such as a Werner 8: Pfieiderer:
  • Example I While the coating composition of Example I functions well when the semi-conducting tape is formed from paper, it may penetrate an open weave fabric unduly. To prevent penetration of Under some conditions the tape the base support, the following composition may be applied:
  • Polyamide 25 Ethyl alcohol 110 Water 45
  • the polyamide used in this example was an N-alkoxymethyl polyhexamethylene adipamide as disclosed above.
  • a single coat of this composition is applied by any suitable rneans to a moderately open weave fabric sheeting. After the base coat has dried, it
  • Example II is treated as in Example I with about 4 ounces per square yard of the composition therein disclosed.
  • Example III Parts by weight N alkoxymethyl polyhexamethylene adipamide 25 Ethyl alcohol 90 Water 36 The resin and solvents are heated and slowly agitated for 12 hours at 140 F. or higher. 75 parts of low resistance carbon black were then added and slow agitation is continued for 12 hours. The mixture is agitated for 1 hour with a high speed agitation. Equal parts of the two compositions, those from the Brubaker patent and the above described N-alkoxymethyl poly amide type, are mixed together, after which coating proceeds as in Examples I and 11. While equal parts yield highly serviceable products, we are not limited to such proportions; our invention comprehends mixtures in all proportions.
  • the time of mixing is important since if the carbon black is entirely surrounded by a film of polyamide, the composition is not sufficiently conducting.
  • the grinding of the carbon black and polyamide mixture should be controlled to give the desired resistance. This time is usually between 6 to 15 hours.
  • the supporting base is coated on one side only. If
  • both sides may be coated or the fabric may be impregnated by drawing it through a bath of the polyamide-carbon black mixture suitably diluted.
  • the paper base may be any suitable type but cable insulating paper sold by Union Mills having a thickness oi! about .003 to .0035 inch is preferred.
  • Suitable fabric is a cotton sheeting of 40 inch width weighing about 6.25 yards per pound. Usually three coats are applied to obtain the necessary thickness although a fewer or greater number may be applied as desired.
  • the particular type of polyamide used is critical and only those which are soluble preferably in an alcoholic solution may be used.
  • the ratio of polyamide to low resistance carbon black should be between .25 and 4 parts of polyamide to each part or carbon black.
  • any of those describedin U. 8. Patents 2,252,554, granted August 12, 1941, 2,252,555, granted August 12, 1941, and 2,252,556, granted August 12, 1941, are likewise suitable. Those melting below about 175 C. are particularly preferred. Examples of these are the multi-component polyamides prepared from hexamethylenediamine, adipic acid, sebacic acid, and caprolactam as described in U. S. Patent 2,285,009, and the alkoxymethyl polyamides such as methoxymethyl hexamethylene adipamide described above. These latter materials may be prepared by the condensation of a polyamide with formaldehyde and an alcohol.
  • polyesteramides formed from combinations of esterand amide-forming reactants, including dibasic acids, diamines, glycols, hydroxy acids; amino acids, and amino alcohols which are described in U. S. Patents 2,071,250, granted February 19, 1937, and 2,312,879, granted March 2, 1943, may be used.
  • Polyesteramides which have been converted to higher molecular weight products by reaction with a diisocyanate as described in U. S. Patent 2,333,639, granted November 9, 1943, are also suitable. Such products may be subsequently converted after calendering to insoluble, infusible products by treating them with formaldehyde or formaldehyde liberating substances.
  • Cables prepared according to the present invention have been found to have an exceptionally long life and maintain uniform electrical characteristics much longer than any heretofore tested.
  • the compositions applied to the tape are particularly resistant to the oil with which the sublayers of paper have been impregnated. The breakdown of the older type materials, rubber, and
  • composition of matter which we have discovered is particularly adaptable to use as a conducting shield for high tension cables, it is also equally useful for other related applications where it is desirable to obtain an electrically conducting surface or film.
  • An oil-impervious semi-conducting tape comprising a flexible supporting base and a semiconducting coating thereon, said coating comprising an alcohol-soluble synthetic linear polyamide having an intrinsic viscosity of at least 0.4, a unit length of at least 7, and an average of at least 2 carbon atoms separating the amide groups, said synthetic linear polyamide being selected from the group which consists of (a) linear polyamides formed by r acting 30-45% of caprolactam, 10-50% of hexamethylenediammonium adipate, and 10-45% of hexamethylenediammonium sebacate, (b) linear polyamides formed by reacting 20-60% of G-aminocaproic acid and not less than 10% each of at least two of the following polyamide-forming compositions: hexamethtylenediammonium sebacate, hexapolyamides formed'by reacting synthetic fiberiorming linear polyamides having hydrogen-bearing amide groups separated by an average of at least 2 carbon
  • An oil-impervious semi-conducting coating composition particularly adapted for the manuiacture of high tension electric cables, comprising an alcohol-soluble synthetic linear polyamide having an intrinsic viscosity of 0.4, a unit length of at least 7, and an average of at least 2 carbon atoms separating the amide groups, said synthetic linear polyamide being selected from the group which consists of (a) linear polyamides formed by reacting 30-45% oi caprolactam, -50% of hexamethylenediammonium adlpate, and 10-45% of hexamethylenediammonium sebacate, (b) linear polyamides formed by reacting 20-60% of 6-aminocaproic acid and not less' than 10% each of at least two 0!
  • the iollowing polyamide-iormv ing compositions hexamethylenediammonium s'ebacate, hexamethylenediammonium adipate, and a mixture of hexamethylenediammonium suberate and hexamethylenediammonium azelate in approximately 15:85-30:70 proportions, and (c) linear polyamides' formed by reacting synthetic fiber-forming linear polyamides having hydrogen-bearing amide groups separated by an average of at least 2 carbon atoms with a mixture of formaldehyde and an alcohol in the presence of an oxygen-containing acid catalyst, and a carbon black having a resistance of less than about 1 ohm per i-inch cube, in the proportion 01 between approximately .25 part and 4 parts of said polyamide to 1 part of said carbon black.
  • a high tension insulated electric cable com- 8 p ising a high tension electric conductor, 'a-iayer oi oil-impregnated insulation therearound, and an oil-impervious organic electric shielding layer over and in contact with the insulation, the shielding layer containing approximately .25 part to 4 parts of an alcohol-soluble synthetic linear nolyamide having an intrinsic viscosity of 0.4, a unit length of at least 7, and an average of at least 2 carbon atoms separating the amide groups,
  • said synthetic linear polyamide being selected from the group which consists of (a) linear polyamides formed by reacting 30-45% of caprolactum, 10-50% oi hexamethylenediammonium adipate, and 10-45% oi. hexamethylene- 'diammonium sebacate, (5) linear polyamides formed by reacting 20-60% of G-aminocaproic acid and not less than 10% each of at least two of the following polyamide-forming compositions: hexamethylenediammonium sebacate, hexamethylenediammonium adipate, and a mixture of hexam'ethylenediammonium suberate and hexamethylenediammonium azelate in approximately 15:85-80:70 proportions, and (0) linear polyamides formed by reacting synthetic fiberforming linear polyamides having hydrogenbearing amide groups separated by an average of at least 2 carbon atoms with a mixture of iormaldehyde and an alcohol in the presence of an

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Description

March 16, 1948. E, PLASS ET L 2,437,708
SEMI-CONDUCTING TAPE FOR ELECTRIC CABLE Filed Feb. 18, 1944 6 .3fm cawwmra 004 ma 4 RUBBER INSULATION 6 I'lV-SUM new 551w- CONDUCT/N6 (04mm;
6' 55m (ma 00mm? WAN/V6 Curtis Edward Plass INVENTORS a'vi Jaseplz jaiivaa Patented Mar. 16, 1948 SEMICONDUCTING TAPE FOR ELECTRIC CABLE Curtis Edward Plass, Worcester, Mass, and David Joseph Sullivan, Fairfleid, Coma; said Sullivan assignor to E. I. du Pont de Nemours & Company, Wilmington, Del., a corporation oi Delaware; said Plass assignor to The American Steel and Wire Company of New Jersey, a corporation of New Jersey Application February 18, 1944, Serial No. 522,980 7 Claims. (Cl. 174-102) This invention relates to a semi-conducting oil impervious coating material for use as an electrostatic shield on high tension insulated electrical conductors where it is desirable to maintain the voltage gradient at the surface of the insulation below a value above which harmful electrical disturbances occur.
Heretofore it has been common to dissipate high voltage charges which surround electric cables carrying high voltages, that is, of the order of 2000 volts or more, by means of a metallic conducting shield over an insulating medium which may be in the form of oil saturated paper, rubber, varnished cambrlc and the like. In ordinary use it is necessary to dissipate or discharge the charges which surround such a cable and this has been doneby various means, such as surrounding the cable with the thin metallic sheath mentioned above. vantage that frequent bendings of the cable tend to develop air gaps because of the separation of the metal shield from the adjacent insulation. When such gaps are formed, arcing across the air gap may occur which eventually causes a failure of the insulating medium or ozone may be formed in the air gap which deleteriously affects the insulation. It has also been proposed to provide a shield which is more flexible than metal. Such shields have been prepared by a conducting paint, compositions of rubber, or other film-forming agents in combination with metallic particles. None of these expedients has been entirely satisfactory when used in combination with oil impregnated insulation due primarily to the attack of the oil on the filmforming agents whereby the conducting properties of the films are deleteriously aflfected.
In U. S. application for Letters Patent Ser. No. 373,181 of Peterson, now Patent No. 2,322,702, granted June 22, 1943, a method for producing satisfactory shielded cables is disclosed. The present invention relates to a modification of the method therein disclosed which oil'ers several desirable advantages, specifically a type of conducting coating or film that embodies enhanced resistance to the solvent action of materials common to cable insulation, permanence of properties when exposed to the effects of aging and electrical discharges, and a means oi. providing a Metals, however, have the disad 2 readily controlled degree of electrical conductivity.
We have now found that many disadvantages of prior art rubber compositions and similar semi-conducting shields have been overcome by the use of a tape having a composition containing a special type of polyamide and a special type of carbon black on its surface or impregnated therewith, especially when used in combination with oil impregnated insulation.
The special types of polyamides are those which are soluble in a lower aliphatic monohydric alcohol, such as those disclosed in U. S. Patent 2,285,009 to Brubaker et al., granted June 2, 1942, and N-alkoxymethyl polyamides disclosed in Cairns application Ser. No. 445,635, filed June 3, 1942 (now abandoned).
The latter are a new class of nitrogen-substituted polyamides formed by reacting with an aldehyde and a formaldehyde-reactive organic compound having a hydrogen attached to an element of groups V and VI of series 2 and 3 of the periodic table, in the presence of an oxygencontaining acid catalyst, polyamides of the general type described in U. S. Patents 2,071,250, 2,071,253 and 2,130,948. The polyamides of this kind, generally speaking, comprise the reaction product of a linear polymer-forming composition containing amide-forming groups, for example, reacting material consisting essentially of bifunctional molecules each containing two reactive groups which are complementary to reactive groups in other molecules and which include complementary amide-forming groups. These polyamides can be obtained by the methods given in the above mentioned patents and by other methods, for example, by self-polymerization of a mono-aminomonocarboxylic acid, by reacting a diamine with a dibasic carboxylic acid in substantially equimolecular amounts, or by reacting a monoaminomonohydric alcohol with a dibasic carboxylic acid in substantially equimolecular amounts, it being understood that reference herein to the amino acids, diamines, dibasic carboxylic acids, and amino alcohols is intended to include the equivalent amide-forming derivatives of these reactants. The preferred polyamides obtained from these reactants have a unit length of at least 7, where unit length is defined as in United States Patents 2,071,253 and 2,130,948. The average number of carbon atoms separating the amide groups in these polyamides is at least two.
' These linear polyamides include also polymers, as for instance the polyester-amides, obtained by admixture of other linear polymer-forming reactants, as for instance glycol-dibasic acid mixtures or hydroxy acids, with the mentioned polyamide-forming reactants. Both the simple and modified linear polyamides contain the recurring amide groups in which X is oxygen or sulfur and R is hydrogen or a monovalent hydrocarbon radical. as an integral part of the main chain of atoms in the polymer. n hydrolysis with hydrochloric acid the amino acid polymers yield the amino acid hydrochloride, and the diamine-dibasic acid polymers yield the diamine hydrochloride and the dibasic carboxylic acid, and the amino alcoholdibasic acid polymers yield the amino alcohol hydrochloride and the dibasic carboxylic acid.
These nitrogen-substituted polyamides are typified by N-methoxymethyl polyhexamethylene adipamide, which was prepared as follows:
A solution of 1 part of polyhexamethylene adipamide (intrinsic viscosity=1.0) in 3.7 parts of formic acid. (commercial grade, specific gravity=1.20) was prepared at 60 C. in a stainless steel reaction vessel equipped with a mechanical stirrer and an opening for the addition of reagents. To this was added at 60 C. a
solution of 1 part paraformaldehyde dissolved inthe mixture as a white granular solid. This .product was removed by filtration, washed thoroughly and dried in vacuum at 50 C.
The carbon black which is used may be prepared according to an article published in "Canadian Chemistry 8: Metallurgy, May, 1933,
pages 93 to 95 by Charles Kaufmann.
In addition to this carbon black, there are now on the market many blacks with high conducting properties. Chapter 7, page 6'7 of the book 00- lumbian Colloidal Carbons, published in. 1938 by the Columbian Carbon Company, defines a suitable type of black as having an electrical resistance in ohms per 1" cube of .152 to .217, al-
though a somewhat higher resistance up to about 1.0 ohm per 1" cube is satisfactory. In the claims such blacks are termed low resistance carbon blacks."
In the drawing Figures 1. 2, and 3 are diagrammatic partial sections of a high tension cable prepared according to the present invention. Figure 4 is a diagrammatic section or a piece of semi-conducting tape. In the drawing, I represents a conductor which may be solid or made up of a bundle of wires as shown. In Figure 1 an oiled paper layer 2 surrounds the conductor l. Over this oiled paper layer is applied a semi-conducting tape made up of a base 3 which may be paper 3 as shown in Figure 1, or the paper may be replaced by a suitable fabric. The tape with the paper or fabric base is provided with a semi-conducting coating 5, The tape is prepared by impregnating or-coating the base with a semi-conducting composition and cut into strips of suitable width, which is then wound around the insulated cable. Figure 2 is a, modification of Figure 1 showing a rubber insulation 4 next to the conductor l instead of the oiled paper shown in Figure 1. The semi-conducting tape also differs from Figure 1 in the cloth base 1 instead of the paper base 3. In Figure 2 the semi-conducting coating is covered with a conventional braid 6.
Figure 3 represents a modification of Figures 1 and 2 in which the semi-conducting tape is applied directly to the copper conductor I. An insulation 8 is provided over the semi-conducting coating 5. This insulation may be rubber shown as 4 in Figure 2 or oiled paper shown as 2 in Figure 1 or other types of electrical insulation. Figure 4 illustrates a section of the semi-conducting tape which has a cloth base 1 and a semi-conducting co'ating 5, the composition of which will be more fully described in the following examples.
In some cases it may be desirable to encase the improved cable or a plurality of such cables in a lead sheath or equivalent protective means ac cording to common practice to make the assembly more impervious to water and more resistant to mechanical abrasion and to function also as a fault current carrying medium to ground.
The resistance of the tape or unsupported layer should be of the order of300 to 1000 Ohms per inch square. may have a resistance of up to 2000 ohms or even more. When a cloth base is used, it is preferable to' coat the same with about 2 to 4 ounces per square yard of polyamide-carbon black com-position. When a paper base is used, about 1 ounce per square .yard is satisfactory, The composition applied to the fabric or paper base may be prepared in any known manner or by methods illustrated by the following examples.
Example I The following ingredients were heated to about F. with stirring for 12 hours in a suitable mixer, such as a Werner 8: Pfieiderer:
Parts by weight Poly-amide prepared according to Example I of U. S. Patent 2,285,009 10 Isopropyl alcohol 30 Water 10 Low resistance carbon black 3 Example I! While the coating composition of Example I functions well when the semi-conducting tape is formed from paper, it may penetrate an open weave fabric unduly. To prevent penetration of Under some conditions the tape the base support, the following composition may be applied:
Parts by weight Polyamide 25 Ethyl alcohol 110 Water 45 The polyamide used in this example was an N-alkoxymethyl polyhexamethylene adipamide as disclosed above.
A single coat of this composition is applied by any suitable rneans to a moderately open weave fabric sheeting. After the base coat has dried, it
is treated as in Example I with about 4 ounces per square yard of the composition therein disclosed.
Example III Parts by weight N alkoxymethyl polyhexamethylene adipamide 25 Ethyl alcohol 90 Water 36 The resin and solvents are heated and slowly agitated for 12 hours at 140 F. or higher. 75 parts of low resistance carbon black were then added and slow agitation is continued for 12 hours. The mixture is agitated for 1 hour with a high speed agitation. Equal parts of the two compositions, those from the Brubaker patent and the above described N-alkoxymethyl poly amide type, are mixed together, after which coating proceeds as in Examples I and 11. While equal parts yield highly serviceable products, we are not limited to such proportions; our invention comprehends mixtures in all proportions.
The time of mixing is important since if the carbon black is entirely surrounded by a film of polyamide, the composition is not sufficiently conducting. The grinding of the carbon black and polyamide mixture should be controlled to give the desired resistance. This time is usually between 6 to 15 hours. In the examples, the supporting base is coated on one side only. If
' desired, both sides may be coated or the fabric may be impregnated by drawing it through a bath of the polyamide-carbon black mixture suitably diluted. The paper base may be any suitable type but cable insulating paper sold by Union Mills having a thickness oi! about .003 to .0035 inch is preferred. Suitable fabric is a cotton sheeting of 40 inch width weighing about 6.25 yards per pound. Usually three coats are applied to obtain the necessary thickness although a fewer or greater number may be applied as desired. After the paper or fabric base is coated, it is cut into convenient widths in the form of a tape which is then used-for wrapping about the conductor in any conventional desired manner. The particular type of polyamide used is critical and only those which are soluble preferably in an alcoholic solution may be used. The ratio of polyamide to low resistance carbon black should be between .25 and 4 parts of polyamide to each part or carbon black.
In addition to the soluble polyamides illustrated in the examples, any of those describedin U. 8. Patents 2,252,554, granted August 12, 1941, 2,252,555, granted August 12, 1941, and 2,252,556, granted August 12, 1941, are likewise suitable. Those melting below about 175 C. are particularly preferred. Examples of these are the multi-component polyamides prepared from hexamethylenediamine, adipic acid, sebacic acid, and caprolactam as described in U. S. Patent 2,285,009, and the alkoxymethyl polyamides such as methoxymethyl hexamethylene adipamide described above. These latter materials may be prepared by the condensation of a polyamide with formaldehyde and an alcohol. While the invention has been illustrated with certain polyamides, the polyesteramides, formed from combinations of esterand amide-forming reactants, including dibasic acids, diamines, glycols, hydroxy acids; amino acids, and amino alcohols which are described in U. S. Patents 2,071,250, granted February 19, 1937, and 2,312,879, granted March 2, 1943, may be used. Polyesteramides which have been converted to higher molecular weight products by reaction with a diisocyanate as described in U. S. Patent 2,333,639, granted November 9, 1943, are also suitable. Such products may be subsequently converted after calendering to insoluble, infusible products by treating them with formaldehyde or formaldehyde liberating substances.
Cables prepared according to the present invention have been found to have an exceptionally long life and maintain uniform electrical characteristics much longer than any heretofore tested. The compositions applied to the tape are particularly resistant to the oil with which the sublayers of paper have been impregnated. The breakdown of the older type materials, rubber,
- etc. is accompanied with an emanation of decomposition products which contaminate the insulating oil and ruin its insulating properties. stability of the nylon base in oil contributes to the longevity of the insulating phase. While the composition of matter which we have discovered is particularly adaptable to use as a conducting shield for high tension cables, it is also equally useful for other related applications where it is desirable to obtain an electrically conducting surface or film.
It is apparent that many widely difierent embodiments of this invention may be made without departing from the spirit and scope thereof; and, therefore, it is not intended to be limited except as indicated in the appended claims.
We claim:
1. An oil-impervious semi-conducting tape comprising a flexible supporting base and a semiconducting coating thereon, said coating comprising an alcohol-soluble synthetic linear polyamide having an intrinsic viscosity of at least 0.4, a unit length of at least 7, and an average of at least 2 carbon atoms separating the amide groups, said synthetic linear polyamide being selected from the group which consists of (a) linear polyamides formed by r acting 30-45% of caprolactam, 10-50% of hexamethylenediammonium adipate, and 10-45% of hexamethylenediammonium sebacate, (b) linear polyamides formed by reacting 20-60% of G-aminocaproic acid and not less than 10% each of at least two of the following polyamide-forming compositions: hexamethtylenediammonium sebacate, hexapolyamides formed'by reacting synthetic fiberiorming linear polyamides having hydrogen-bearing amide groups separated by an average of at least 2 carbon atoms with a mixture of formaldehyde and an alcohol in the presence of an oxygen-containing acid catalyst, and a carbon blackwhich has a resistance of less than about 1 ohm per 1-inch cube, these component being present in the ratio or between approximately.25 and 4 parts of said polyamide to 1 part of said carbon black 2. The semi-conducting tape of claim 1,- in which the polyamide is a polyester-amide having a melting point below 175 0.
3. The semi-conducting tape of claim 1, in which the base is a rabric base.
4. ,The semi-conducting tape of claim 1, in which the base is a paper base.
5. An oil-impervious semi-conducting coating composition, particularly adapted for the manuiacture of high tension electric cables, comprising an alcohol-soluble synthetic linear polyamide having an intrinsic viscosity of 0.4, a unit length of at least 7, and an average of at least 2 carbon atoms separating the amide groups, said synthetic linear polyamide being selected from the group which consists of (a) linear polyamides formed by reacting 30-45% oi caprolactam, -50% of hexamethylenediammonium adlpate, and 10-45% of hexamethylenediammonium sebacate, (b) linear polyamides formed by reacting 20-60% of 6-aminocaproic acid and not less' than 10% each of at least two 0! the iollowing polyamide-iormv ing compositions: hexamethylenediammonium s'ebacate, hexamethylenediammonium adipate, and a mixture of hexamethylenediammonium suberate and hexamethylenediammonium azelate in approximately 15:85-30:70 proportions, and (c) linear polyamides' formed by reacting synthetic fiber-forming linear polyamides having hydrogen-bearing amide groups separated by an average of at least 2 carbon atoms with a mixture of formaldehyde and an alcohol in the presence of an oxygen-containing acid catalyst, and a carbon black having a resistance of less than about 1 ohm per i-inch cube, in the proportion 01 between approximately .25 part and 4 parts of said polyamide to 1 part of said carbon black.
6. A high tension insulated electric cable com- 8 p ising a high tension electric conductor, 'a-iayer oi oil-impregnated insulation therearound, and an oil-impervious organic electric shielding layer over and in contact with the insulation, the shielding layer containing approximately .25 part to 4 parts of an alcohol-soluble synthetic linear nolyamide having an intrinsic viscosity of 0.4, a unit length of at least 7, and an average of at least 2 carbon atoms separating the amide groups,
said synthetic linear polyamide being selected from the group which consists of (a) linear polyamides formed by reacting 30-45% of caprolactum, 10-50% oi hexamethylenediammonium adipate, and 10-45% oi. hexamethylene- 'diammonium sebacate, (5) linear polyamides formed by reacting 20-60% of G-aminocaproic acid and not less than 10% each of at least two of the following polyamide-forming compositions: hexamethylenediammonium sebacate, hexamethylenediammonium adipate, and a mixture of hexam'ethylenediammonium suberate and hexamethylenediammonium azelate in approximately 15:85-80:70 proportions, and (0) linear polyamides formed by reacting synthetic fiberforming linear polyamides having hydrogenbearing amide groups separated by an average of at least 2 carbon atoms with a mixture of iormaldehyde and an alcohol in the presence of an oxygen-containing acid catalyst, to 1 part of a carbon black which has a resistance ,of less than about 1 ohm per l-inch cube.
7. The article of claim 6, in which the resistance oi the polyamide-carbon black mixture is between 300 and 2,000 ohms per square inch.
CURTIS EDWARD PLA SS. DAVID JOSEPH SULLIVAN.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS OTHER REFERENCES Pages 146 to 157, Rubber Chemistry and Technology, vol. 15. 1942. (Copy in Div. 50.)
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Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2679569A (en) * 1951-08-25 1954-05-25 Electrofilm Corp Electrically conductive film
US2795680A (en) * 1952-05-16 1957-06-11 Sprague Electric Co Printed resistors and inks
US2933457A (en) * 1956-04-02 1960-04-19 Gen Cable Corp Method of forming semi-conductive nylon lacquer
US3125738A (en) * 1964-03-17 Electronic organ key
US4064075A (en) * 1972-08-11 1977-12-20 E. I. Du Pont De Nemours And Company Conductive, extrudable polymer composition of poly(ε-caproamide) and carbon black
US4153582A (en) * 1976-04-30 1979-05-08 Ceskoslovenska Akademie Ved Method for the preparation of polymers of lactams having an enhanced electric conductivity
US5807447A (en) * 1996-10-16 1998-09-15 Hendrix Wire & Cable, Inc. Neutral conductor grounding system
US10872712B2 (en) 2017-11-07 2020-12-22 Hitachi Metals, Ltd. Insulated wire
US11205525B2 (en) * 2017-11-07 2021-12-21 Hitachi Metals, Ltd. Insulated wire

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2068940A (en) * 1934-06-23 1937-01-26 Okonite Co Electric cable
US2282832A (en) * 1939-11-24 1942-05-12 Gen Electric Semiconducting tape
US2285009A (en) * 1941-02-24 1942-06-02 Du Pont Interpolyamide
US2322702A (en) * 1929-06-24 1943-06-22 Thomas F Peterson Shielded cable
US2333922A (en) * 1941-07-14 1943-11-09 Du Pont Insulated electrical conductor

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2322702A (en) * 1929-06-24 1943-06-22 Thomas F Peterson Shielded cable
US2068940A (en) * 1934-06-23 1937-01-26 Okonite Co Electric cable
US2282832A (en) * 1939-11-24 1942-05-12 Gen Electric Semiconducting tape
US2285009A (en) * 1941-02-24 1942-06-02 Du Pont Interpolyamide
US2333922A (en) * 1941-07-14 1943-11-09 Du Pont Insulated electrical conductor

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3125738A (en) * 1964-03-17 Electronic organ key
US2679569A (en) * 1951-08-25 1954-05-25 Electrofilm Corp Electrically conductive film
US2795680A (en) * 1952-05-16 1957-06-11 Sprague Electric Co Printed resistors and inks
US2933457A (en) * 1956-04-02 1960-04-19 Gen Cable Corp Method of forming semi-conductive nylon lacquer
US4064075A (en) * 1972-08-11 1977-12-20 E. I. Du Pont De Nemours And Company Conductive, extrudable polymer composition of poly(ε-caproamide) and carbon black
US4153582A (en) * 1976-04-30 1979-05-08 Ceskoslovenska Akademie Ved Method for the preparation of polymers of lactams having an enhanced electric conductivity
US5807447A (en) * 1996-10-16 1998-09-15 Hendrix Wire & Cable, Inc. Neutral conductor grounding system
US6046408A (en) * 1996-10-16 2000-04-04 Hendrix Wire & Cable, Inc. Neutral conductor grounding system
US10872712B2 (en) 2017-11-07 2020-12-22 Hitachi Metals, Ltd. Insulated wire
US11205525B2 (en) * 2017-11-07 2021-12-21 Hitachi Metals, Ltd. Insulated wire

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