Process for producing a lubricant coated laquered wire used for forming the stator winding of an electrical refrigerating compressor

Information

  • Patent Grant
  • 6562767
  • Patent Number
    6,562,767
  • Date Filed
    Monday, February 12, 1996
    28 years ago
  • Date Issued
    Tuesday, May 13, 2003
    21 years ago
Abstract
A lubricant for wire, which is insulated by means of a lacquer coating, and which is used for forming the stator windings of an electrical refrigerating compressor, consists of one or more compounds of the formula CH3—Xn—R, wherein X is a linear or branched hydrocarbon group with n carbon atoms, wherein n is up to 22, and R may be hydrogen or a plurality of different radicals, either in a pure form or dissolved in a suitable solvent. The lubricant is applied to the wire to reduce its coefficient of friction, and it is remarkable for its compatibility with the environmentally unharmful refrigerants, such as R134a (1,1,1,2-tetrafluoroethane), which are used today in refrigerating compressors without capillary tube obstructions.
Description




The present invention concerns a lubricant for wire which is used for forming the stator windings of an electrical refrigerating compressor. The wire consists of a conductor coated with an electrically insulating layer on which a lubricant is applied to reduce the coefficient of friction of the wire. Of course, such a lubricant must have the lubricating properties necessary for the intended use, but must moreover be compatible with the refrigerant used in the refrigerating compressor.




It is known from the DE Offenlegungsschrift 1947071 and the GB Patent Specifications 1175059 and 1175060 to provide electrical cables with lubricants for the purpose of reducing the mutual friction between the cables. When such a lubricant is added to the insulating layer around the conductor, a single cable among many cables, e.g. telephone cables in the same pipe can readily be removed or introduced, because the coefficient of friction of the individual cables is reduced considerably.




The preferred lubricant added to the insulating layer of polyolefin according to the above-mentioned documents is an amide which is added in various amounts and using various additives to the insulating layer before this layer is applied around the conductor.




The U.S. Pat. Nos. 4,348,460, 4,350,737, 4,350,738, 4,385,436, 4,385,437, 4,390,590, 4,410,592 and 4,449,290 separately concern lubricants for wire which is used for forming the stator windings of electrical motors. These patent specifications describe the general problems which are associated with automatic mounting of the stator windings, including the importance of the wires having a suitably low coefficient of friction. This is necessary to avoid mechanical damage to the wires, e.g. by rubbing, by mounting in the slots in the stator.




The patent specifications also describe how the lubricant used for the wires may cause problems in connection with refrigerating compressors, because the lubricant precipitates from the solution when this contacts the refrigerant used in the refrigerating system. The precipitated lubricant will hereby be moved about in the refrigerating system, which involves capillary tube obstructions. This is obviated according to the above-mentioned US patent specifications by completely removing the lubricant by heating following mounting of the windings.




The lubricants used according to the above-mentioned US patent specifications may be mixtures of paraffin wax, triglycerides and esters having a lubricating effect. Such a mixture is added by moving the wire, which has been provided with an insulating layer beforehand, across two pieces of felt which are dipped in the mixture. The lubricants may moreover be bees' wax which is applied to various types of insulation layers, such as nylon or I polyamide imide, optionally in mixture with oleic acid and surfactants.




It is moreover known that paraffin may be used as a lubricant for wire in connection with the manufacture of electrical refrigerating compressors. This lubricant is excellent in its present form in connection with the classic refrigerant R12 (Freon®12), dichlorodifluoro-methane CCl


2


F


2


). However, this refrigerant has been found to deplete the ozone layer in the atmosphere, and its use will therefore be banned (in all EEC countries as from Jan. 1, 1997). Instead of R12 less environmentally harmful refrigerants will be used, primarily the refrigerant R134a (1,1,1,2-tetrafluoroethane CF


3


CH


2


F), alone or in mixture with other refrigerants.




However, it has been found that the paraffin used till now is not soluble in the refrigerant R134a, but, on the contrary, precipitates when the temperature drops. This results in capillary tube obstructions.




When it is known beforehand that precipitation of the lubricant will take place, capillary tube obstructions can be avoided by removing the lubricant after mounting of the wound wires, as described e.g. in the above-mentioned U.S. Pat. No. 4,350,737. However, such a removal is a process adding to the costs and for the used lubricant to be removed completely it is often necessary to use cleaning agents which are harmful to the environment.




Conclusively, a lubricant for the wire in a refrigerating compressor is to satisfy the following requirements: (1) It is to give such a small coefficient of friction that the wire will not be mechanically damaged during winding and mounting, and (2) it must not be capable of releasing substances that can damage the refrigerating system or the compressor. Finally, (3) it must possible to add to it a solvent which is environmentally unharmful.




The DE Auslegeschrift 1011109 and the EP Patent Application 0445611 disclose dialkyl esters of di- or polycar-boxylic acids, which maybe used as lubricants, and which, as regards some of them, are soluble in e.g. the refrigerant R134a. However, these lubricants are exclusively used for lubricating the movable mechanical parts in the compressor in operation, and, usually, the lubricants are present in a lubricating sump in the compressor, from which they might be circulated through the cooling system and should therefore be soluble in the refrigerant used.




The lubricant of the invention, however, is not a lubricant in the above-mentioned sense, but, in contrast, is an agent to be applied to the wire, which is used for forming the stator windings in a refrigerating compressor. As mentioned above, to be useful for this purpose, the lubricants must satisfy three requirements, which must be met simultaneously, which is not the case with the lubricants known from the above-mentioned DE Auslegeschrift and EP Patent Application.




It has now surprisingly been found that a group of compounds are active as lubricants capable of satisfying the above-mentioned requirements, and that these compounds are compatible with the new refrigerants which spare the ozone layer.




Thus, the invention concerns a lubricant for wire which is used for forming the stator windings of an electrical refrigerating compressor, said wire being coated with an electrically insulating layer, and the lubricant of the invention is characterized in that it consists of one or more compounds of the general formula






CH


3


—X


n


—R






wherein X is a linear or branched hydrocarbon group with n carbon atoms and optionally containing one or more double bonds, and R is




(a) hydrogen, in which case n is 16-22;




(b) —COOR , wherein R


1


is C


1


-C


4


alkyl, in which case n is 15-19;




(c) —OOC—R


2


—COOR


3


, wherein R


2


is C


8


-C


10


alkyl and R


3


is C


1


-C


4


alkyl, in which case n is 0-3;




(d)











 wherein R


4


and R


5


are separately hydrogen or C


1


-C


2


alkyl, in which case n is 12-18;




(e)











 wherein R


6


and R


7


are separately hydrogen or C


4


-C


8


alkyl, in which case n is 0-3;




(f) a group of the formula











 in which case n is 8-14;




(g) a group of the formula











 in which case n is 8-14;




(h) a group of the formula











 wherein R


8


is hydrogen or C


1


-C


2


alkyl, in which case n is 6-11 or




(i) a group of the formula











 wherein R


9


is hydrogen or C


1


-C


2


alkyl, in which case n is 1-5,




either in pure form or dissolved in a suitable solvent.




Useful solvents are e.g. test petrol, butanol, propanol and ethanol.




The use of the present lubricants firstly provides extremely good lubricating properties, and secondly problems of capillary tube obstructions are avoided because the lubricants are compatible with the new environmentally unharmful polar refrigerants, such as the above-mentioned R134a (CF


3


CH


2


F) and R124 (CHClFCF


3


), R125 (CHF


2


CF


3


), R152a (CHF


2


CH


3


) as well as mixtures thereof. Consequently, it is not necessary either to remove the lubricant from the wire after completed winding.




In connection with the present invention no requirements are made of the wire used beyond the requirements generally made of wire to be used for forming stator windings in an electrical refrigerating compressor. The insulating layer surrounding the wire is typically a lacquer, which is just to satisfy the requirements that it is to be compatible with and resistant to the refrigerant used, and that it is to be heat- and cold-resistant.




The lacquer may e.g. a polyester imide which is suitably modified with tris-hydroxyethyl isocyanurate (THEIC) for the purpose of making the lacquer resistant to the refrigerant. The lacquer may also be of the two-layer type which consists of a primer of a polyester imide with a top coat of a polyamide imide.




The coefficient of friction of the wire after application of the lubricant is measured according to the standard DIN 46453, and values of below 0.15 are required to satisfy the requirement with respect to avoiding damage during winding and mounting of the stator.




The compounds of the formula shown above may be a plurality of different chemical compounds, more particularly paraffins, esters of carboxylic acids, diesters of dicarboxylic acids, amides of carboxylic acids, urethanes (carbamates), derivatives of γ- and δ-lactams and derivatives of γ- and δ-lactones.











The invention will be illustrated more fully by the following examples:




EXAMPLE 1




The lubricant is a paraffin which consists of a mixture of alkanes having the chain length 18 to 20 carbon atoms and has the formula:






CH


3


(CH


2


)


16-18


CH


3








The solubility of the paraffin, melting in the range 29-33° C., with respect to the refrigerant R134A is evaluated by means of the method according to the standard DIN 51 331. It has been found that 50 mg can be dissolved in 100 g of R134a down to −45° C. 50 g of the paraffin are dissolved in 15 liters of petrol (boiling point 110-130° C.), and the solution is applied to a wire coated with lacquer of the polyester imide type suitably modified with THEIC. Application is performed by means of pieces of felt. After evaporation of the petrol, coefficients of friction of 0.14-0.15 sufficiently low to prevent mechanical damage to the wire are obtained.




EXAMPLE 2




The lubricant is stearic acid methyl ester of the formula






CH


3


(CH


2


)


16


COOCH


3








dissolved in ethanol. It has been found that 50 mg of the ester can be dissolved in 100 g of R134a down to −45° C., which is the necessary amount in a motor. 10 g of stearic acid methyl ester are dissolved in 15 liters of ethanol, and the solution is applied to a wire coated with lacquer of the polyester imide type suitably modified with THEIC. Application is performed by means of pieces of felt. After the ethanol has evaporated, coefficients of friction of 0.14-0.15 sufficiently low to prevent mechanical damage to the wire are obtained.




EXAMPLE 3




The lubricant is azelaic acid dibutyl ester of the formula






C


4


H


7


—OOC(CH


2


)


7


COO—C


4


H


7








whose solubility with respect to the refrigerant R134a is evaluated by means of the method according to the standard DIN 51 311. It has been found that 100 mg can be dissolved in 100 g of R134a down to −45° C. 120 g of the diester are dissolved in 15 liters of ethanol, and the solution is applied to a wire coated with lacquer of the polyester imide type suitably modified with THEIC. Application is performed by means of pieces of felt. After evaporation of the ethanol, coefficients of friction of 0.14-0.15 sufficiently low to prevent mechanical damage to the wire are obtained.




EXAMPLE 4




The lubricant is a carboxylic acid amide of the formula











whose solubility with respect to the refrigerant R134a is evaluated by means of the method according the standard DIN 51 331. It has been found that 100 mg can be dissolved in 100 g of R134a down to −45° C. 120 g of the carboxyl amide are dissolved in 15 liters of ethanol, and the solution is applied to a wire coated with lacquer of the polyester imide type suitably modified with THEIC. Application is performed by means of pieces of felt. After evaporation of the ethanol, coefficients of friction of 0.14-0.15 sufficiently low to prevent mechanical damage to the wire are obtained.




EXAMPLE 5




The lubricant is N,N-dimethylpentyl carbamate of the formula






(CH


3


)


2


NCOOC


5


H


11








whose solubility with respect to the refrigerant R134a is evaluated by means of the method according to the standard DIN 51 331. It has been found that 150 mg can be dissolved in 100 g of R134a down to −45° C. 120 g of the carbamate are dissolved in 15 liters of ethanol, and the solution is applied to a wire coated with lacquer of the polyester imide type suitably modified with THEIC. Application is performed by means of pieces of felt. After evaporation of the ethanol, coefficients of friction of 0.14-0.15 sufficiently low to prevent mechanical damage to the wire are obtained.




EXAMPLE 6




The lubricant is palmitic acid methyl ester of the formula






CH


3


(CH


2)




14


COOCH


3








dissolved in ethanol. It has been found that 50 mg of the ester can be dissolved in 100 g of R134a down to −55° C. 10 g of palmitic acid methyl ester are dissolved in 15 liters of ethanol, and the solution is applied to a wire coated with lacquer of the polyester imide type suitably modified with THEIC. Application is performed by means of pieces of felt. After the ethanol has evaporated, coefficients of friction of 0.14-0.15 sufficiently low to prevent mechanical damage to the wire are obtained.



Claims
  • 1. A process for forming a wire in the stator windings of an electrical refrigerating compressor using a refrigerant comprising the steps of:(1) coating said wire with an electrically insulating layer compatible with and resistant to said refrigerant; (2) coating said electrically insulating layer with a lubricant to give it a low coefficient of friction so that said wire will not be mechanically damaged during winding and rewinding; (3) winding and mounting said wire in said stator windings; and (4) after winding and mounting said wire in said stator windings, preventing damage to the refrigerating system or the compressor by exposing said lubricant to a compatible refrigerant/refrigeration system.
  • 2. A process for forming a wire according to claim 1 wherein said lubricant consists of at least one compound of the general formulaCH3—Xn—R wherein X is a linear or branched hydrocarbon group with n carbon atoms and optionally containing one or more double bonds, and R is selected from the group consisting of(a) hydrogen, in which case n is 16-22; (b) —COOR1, wherein R1 is C1-C4 alkyl, in which case n is 14-19; (c) —OOC—R2—COOR3, wherein R2 is C7-C10 alkyl and R3 is C1-C4 alkyl, in which case n is 0-3; (d)  wherein R4 and R5 are separately hydrogen or C1-C2 alkyl, in which case n is 12-18; (e)  wherein R6 and R7 are separately hydrogen or C4-C8 alkyl, in which case n is 0-3; (f) a group of the formula  in which case n is 8-14; (g) a group of the formula  in which case n is 8-14; (h) a group of the formula  wherein R8 is hydrogen or C1-C2 alkyl, in which case n is 6-11 or (i) a group of the formula  wherein R9 is hydrogen or C1-C2 alkyl, in which case n is 1-5.
  • 3. A process for forming a coated wire according to claim 2, in which the lubricant is applied to the wire by means of pieces of cotton or felt.
  • 4. A process according to claim 2, in which said lubricant is further dissolved in a solvent and said solvent is selected from the group consisting of petrol, butanol, ethanol and propanol.
  • 5. A process according to claim 2 in which the lubricant is a carboxylic acid amide of the general formula wherein Xn, R4 and R5 are as defined in claim 2.
  • 6. A process according to claim 5, in which Xn is —(CH2)15—, and R4 and R5 are hydrogen.
  • 7. A process according to claim 2, in which the lubricant is a carboxylic acid alkyl ester of the general formulaCH3—Xn—COOR1 wherein Xn and R1 are as defined in claim 2.
  • 8. A process according to claim 7, in which Xn is —(CH2)16—, and R1 is methyl.
  • 9. A process according to claim 7, in which Xn is —(CH2)14—, and R1 is methyl.
  • 10. A process according to claim 4 including ethanol used as a solvent in which said amide is further dissolved in ethanol as a solvent.
  • 11. A process according to claim 4 wherein ethanol is used as a solvent in which said ester is further dissolved.
Priority Claims (1)
Number Date Country Kind
1664/91 Sep 1991 DK
Parent Case Info

This application is a continuation of application Ser. No. 08/211,045, filed Mar. 11, 1994, now abandoned.

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Provisional Applications (1)
Number Date Country
PCT/DK92/00284 Sep 1993 US
Continuations (1)
Number Date Country
Parent 08/211045 Mar 1994 US
Child 08/599668 US