Conductors having insulation of polyester imide resin

Claim 2

An insulated electrical conductor comprising in combination, an electrical conductor and a cured polyester imide resin coating said electrical conductor, said polyester imide resin having ester groups of acid and alcohol moieties in the chain which are condensation products of at least difunctional carboxylic acid or a derivative thereof which is a functionally active equivalent, and at least difunctional alcohol or a derivative thereof which is a functionally active equivalent, and between said ester groups, moieties containing a 5-membered imide ring and which are condensation products of an aromatic carboxylic acid anhydride containing a 5-membered cyclic carboxylic anhydride group or a derivative thereof which is a functionally active equivalent and at least one additional reactable group, and a primary amine or a derivative thereof which is a functionally active equivalent, containing at least one additional reactable group.

Claim 3

Insulated electrical conductor according to claim 1, said additional reactable group of the anhydride being carboxyl, carboxylic acid anhydride, or hydroxyl.

Claim 4

Insulated electrical conductor according to claim 1, said additional reactable group of the amine being carboxyl, hydroxyl or primary amino.

Claim 5

Insulated electrical conductor according to claim 2, said additional reactable group of the amine being carboxyl, hydroxyl or primary amino.

Claim 6

Insulated electrical conductor according to claim 1, said alcohol moieties including residues of ethylene glycol.

Claim 7

Insulated electrical conductor according to claim 1, said alcohol moieties including residues of glycerine.

Claim 8

Insulated electrical conductor according to claim 5, said alcohol moieties including residues of glycerine.

Claim 9

Insulated electrical conductor according to claim 1, the percentage of imide groups based on the sum of ester and imide groups being 9.4-50%.

Claim 10

Insulated electrical conductor according to claim 1, the additional reactable group of the aromatic carboxylic acid anhydride being a carboxyl group.

Claim 11

Insulated electrical conductor according to claim 1, the additional reactable group of the aromatic carboxylic acid anhydride being a anhydride group.

Claim 12

Insulated electrical conductor according to claim 1, the additional reactable group of the aromatic carboxylic acid anhydride being a hydroxyl group.

Claim 13

Insulated electrical conductor according to claim 1, the additional reactable group of the amine being a carboxyl group.

Claim 14

Insulated electrical conductor according to claim 1, the additional reactable group of the amine being a hydroxyl group.

Claim 15

Insulated electrical conductor according to claim 1, the additional reactable group of the amine being a primary amino group.

Claim 16

Insulated electrical conductor according to claim 1, said aromatic carboxylic anhydride being trimellitic acid anhydride, pyromellitic acid anhydride or dianhydride of tetracarboxylic acid having two benzene nucleii in the molecule.

Claim 17

Insulated electrical conductor according to claim 1, said aromatic carboxylic acid anhydride being trimellitic acid anhydride, said amine being a diprimary amine, said anhydride and amine being in the proportion of 2:1, anhydride:amine.

Claim 18

Insulated electrical conductor according to claim 1, said aromatic carboxylic acid anhydride being trimellitic acid anhydride, said amine being a primary amino carboxylic acid, said anhydride and amine being in the proportion of 1:1.

Claim 19

Insulated electrical conductor according to claim 1, said aromatic carboxylic acid anhydride being a tetracarboxylic acid dianhydride, said amine being a primary amino carboxylic acid, said anhydride and amine being used in the proportion of 1:2, anhydride:amine.

Claim 20

Conductor of claim 1, the alcohol moieties including residues of polyhydric alcohols having three hydroxy groups.

Claim 21

Conductor of claim 19, said alcohol moieties including residues of ethylene glycol.

Claim 22

Method of coating an electrical conductor with electrically insulating enamel which comprises passing the conductor through an enameling lacquer comprising a resin for forming the enamel and a cresol type solvent, to coat the conductor with a film of the enameling lacquer, and thereafter heating the coated conductor to cure the resin and drive off the solvent, said resin being a polyester imide resin having ester groups of acid and alcohol moieties in the chain which are condensation products of at least difunctional carboxylic acid or a derivative thereof which is a functionally active equivalent, and at least difunctional alcohol or a derivative thereof which is a functionally active equivalent, and, between said ester groups, an amount effective to improve the thermal stability of the resin without rendering the resin insoluble to the extent which would make it unsuitable for use in a wire lacquer composed of the resin dissolved in cresol and solvent naphtha, of moieties containing a 5 membered imide ring and which are condensation products of an aromatic carboxylic acid anhydride containing a 5-membered cyclic carboxylic acid anhydride group or a derivative thereof which is a functionally active equivalent and at least one additional reactable group, and a primary amine or a derivative thereof which is a functionally active equivalent, containing at least one additional reactable group.

Claim 23

Method of coating an electrical conductor with electrically insulating enamel which comprises passing the conductor through an enameling lacquer comprising a resin for forming the enamel and a cresol type solvent, to coat the conductor with a film of the enameling lacquer, and thereafter heating the coated conductor to cure the resin and drive off the solvent, said resin being a polyester imide resin having ester groups of acid and alcohol moieties in the chain which are condensation products of at least difunctional carboxylic acid or a derivative thereof which is a functionally active equivalent, and at least difunctional alcohol or a derivative thereof which is a functionally active equivalent, and, between said ester groups, an amount effective to improve the thermal stability of the resin without rendering the resin insoluble to the extent which would make it unsuitable for use in a wire lacquer composed of the resin dissolved in cresol and solvent naphtha, of moieties containing a 5 membered imide ring and which are condensation products of an aromatic carboxylic acid anhydride containing a 5-membered cyclic carboxylic acid anhydride group or a derivative thereof which is a functionally active equivalent and at least one additional reactable group, and a primary amine or a derivative thereof which is a functionally active equivalent, containing at least one additional reactable group.

Claim 24

Method according to claim 21, said additional reactable group of the anhydride being carboxyl, carboxylic acid anhydride, or hydroxyl.

Claim 25

Method according to claim 21, said additional reactable group of the amine being carboxyl, hydroxyl or primary amino.

Claim 26

Method according to claim 22, said additional reactable group of the amine being carboxyl, hydroxyl or primary amino.

Claim 27

Method according to claim 21, said alcohol moieties including residues of ethylene glycol.

Claim 28

Method according to claim 21, said alcohol moieties including residues of glycerine.

Claim 29

Method according to claim 25, said alcohol moieties including residues of glycerine.

Claim 30

Method according to claim 21, the percentage of imide groups based on the sum of ester and imide groups being 9.4-50%.

Claim 31

Method according to claim 21, the additional reactable group of the aromatic carboxylic acid anhydride being a carboxyl group.

Claim 32

Method according to claim 21, the additional reactable group of the aromatic carboxylic acid anydride being an anhydride group.

Claim 33

Method according to claim 21, the additional reactable group of the aromatic carboxylic acid anhydride being a hydroxyl group.

Claim 34

Method according to claim 21, the additional reactable group of the amine being a carboxyl group.

Claim 35

Method according to claim 21, the additional reactable group of the amine being a hydroxyl group.

Claim 36

Method according to claim 21, the additional reactable group of the amine being a primary amino group.

Claim 37

Method according to claim 21, said aromatic carboxylic anhydride being trimellitic acid anhydride, pyromellitic acid anhydride or dianhydride of tetracarboxylic acid having two benzene nucleii in the molecule.

Claim 38

Method according to claim 21, said aromatic carboxylic acid anhydride being trimellitic acid anhydride, said amine being a diprimary aromatic amine, said anhydride and amine being in the proportion of 2:1, anhydride:amine.

Claim 39

Method according to claim 21, said aromatic carboxylic acid anhydride being trimellitic acid anhydride, said amine being a primary amino carboxylic acid, said anhydride and amine being in the proportion of 1:1.

Claim 40

Method according to claim 21, said aromatic carboxylic acid anhydride being a tetracarboxylic acid dianhydride, said amine being a primary amine carboxylic acid, said anhydride and amine being used in the proportion of 1:2, anhydride:amine.

Claim 41

Method of claim 21, the alcohol moieties including residues of polyhydric alcohols having more than two hydroxy groups.

Claim 42

Method of claim 39, said alcohol moieties including residues of ethylene glycol.

Claim 43

Method of claim 21, the alcohol moieties including residues of polyhydric alcohols having three hydroxy groups.

Claim 44

Method of claim 21, said alcohol moieties including residues of ethylene glycol and residues of alcohols having three hydroxy groups.