JP7525806B2 - Covered electric wire and method for producing the same - Google Patents

Description

This disclosure relates to a coated electric wire and a method for manufacturing the coated electric wire.

Patent document 1 describes an electric wire having a conductor and a first insulating layer formed on the outer periphery of the conductor, the first insulating layer being made of a thermosetting resin and a fluororesin, with the mass ratio of the thermosetting resin to the fluororesin being 90:10 to 10:90, and being formed by mixing a thermosetting resin solution with a fluororesin organosol, applying the resulting mixture onto the conductor, and baking it.

International Publication No. 2011/024809

The objective of this disclosure is to provide a coated electric wire that exhibits a low dielectric constant and a high partial discharge inception voltage, is resistant to wrinkles in the coating layer even when bent, and has high adhesion strength between the rectangular electric wire substrate and the coating layer.

According to the present disclosure, there is provided a coated electric wire comprising a rectangular electric wire substrate and a coating layer formed on the outer periphery of the rectangular electric wire substrate, the coating layer comprising a first layer formed from a polymer compound (1) having either one or both of an amide group and an imide group, and a water-based paint composition (1) containing a fluorine-containing polymer compound (1), or a powder paint composition (1) containing a polymer compound (1) having either one or both of an amide group and an imide group, and a fluorine-containing polymer compound (1), and a second layer formed from a water-based paint composition (2) containing a fluorine-containing polymer compound (2-1), or a powder paint composition (2) containing a fluorine-containing polymer compound (2-2).

According to the present disclosure, it is possible to provide a coated electric wire that exhibits a low relative dielectric constant and a high partial discharge inception voltage, is less likely to cause wrinkles in the coating layer even when bent, and has high adhesion strength between the rectangular electric wire substrate and the coating layer.

Specific embodiments of the present disclosure are described in detail below, but the present disclosure is not limited to the following embodiments.

The coated electric wire of the present disclosure includes a rectangular electric wire substrate and a coating layer formed on the outer periphery of the rectangular electric wire substrate.

(Rectangular electric wire substrate)
The shape of the rectangular electric wire substrate is not particularly limited as long as the cross section is a rectangular wire shape. The corners of the cross section of the rectangular electric wire substrate may be right angles, or the corners of the cross section of the rectangular electric wire substrate may be rounded. In addition, the rectangular electric wire substrate may be a single wire, a stranded wire, a twisted wire, or the like, as long as the cross section of the entire substrate is approximately rectangular, but a single wire is preferable.

The rectangular electric wire substrate is not particularly limited as long as it is made of a conductive material, but it can be made of materials such as copper, copper alloy, aluminum, aluminum alloy, iron, silver, nickel, etc., and is preferably made of copper, copper alloy, aluminum or aluminum alloy. It is also possible to use rectangular electric wire substrates that are plated with silver plating, nickel plating, etc. As the copper, oxygen-free copper, low-oxygen copper, copper alloy, etc. can be used.

The cross-sectional width of the rectangular electric wire substrate may be 1 to 75 mm, and the cross-sectional thickness of the rectangular electric wire substrate may be 0.1 to 30 mm. The outer circumferential diameter of the rectangular electric wire substrate may be 6.5 mm or more and 200 mm or less. The ratio of width to thickness may be greater than 1 and less than 30.

The surface roughness Sz of the rectangular electric wire substrate is preferably 0.2 to 12 μm, more preferably 1 μm or more, even more preferably 5 μm or more, and more preferably 10 μm or less, so that the rectangular electric wire substrate and the coating layer are more firmly adhered to each other.

The surface roughness of the rectangular electric wire substrate can be adjusted by subjecting the rectangular electric wire substrate to a surface treatment such as etching, blasting, or laser treatment. In addition, the surface of the rectangular electric wire substrate may be provided with irregularities by surface treatment. The smaller the distance between the irregularities from one convex portion to the other convex portion, the more preferable, for example, 5 μm or less. In addition, the size of the irregularities is, for example, 1 ^μm2 or less per concave portion when the convex portion is cut from the unprocessed surface. The irregularity shape may be a single crater-type irregularity shape, or may be branched in an ant nest shape.

(Covering layer)
The covering layer included in the covered electric wire of the present disclosure includes at least a first layer and a second layer. In the covered electric wire of the present disclosure, the first layer is usually formed on the outer periphery of the rectangular electric wire substrate, and the second layer is formed on the outer periphery of the first layer.

The first layer and the second layer are both coatings formed from a coating composition. The first layer is a coating formed from a water-based coating composition (1) or a powder coating composition (1). The second layer is a coating formed from a water-based coating composition (2) or a powder coating composition (2).

A water-based coating composition contains water as a solvent together with a polymer compound or a fluorine-containing polymer compound. A powder coating composition contains a powder of a polymer compound or a fluorine-containing polymer compound. In this disclosure, the term "powder coating composition" is used even when the powder coating contains only a powder of a polymer compound or only a powder of a fluorine-containing polymer compound, i.e., even when the powder coating does not contain multiple components.

The water-based paint composition (1) contains a polymer compound (1) having either or both of an amide group and an imide group, and a fluorine-containing polymer compound (1). By applying the water-based paint composition (1) to the outer periphery of a rectangular electric wire substrate to form a first layer, it is possible to form a first layer that adheres to the rectangular electric wire substrate with high adhesion strength, and thereby to form a coating layer that adheres to the rectangular electric wire substrate with high adhesion strength, and a coating layer that is less likely to wrinkle even when bent.

The powder coating composition (1) contains a polymer compound (1) having either or both of an amide group and an imide group, and a fluorine-containing polymer compound (1). By applying the powder coating composition (1) to the outer periphery of a rectangular electric wire substrate to form a first layer, it is possible to form a first layer that adheres to the rectangular electric wire substrate with high adhesion strength, and thereby to form a coating layer that adheres to the rectangular electric wire substrate with high adhesion strength, and that is less likely to wrinkle even when bent.

The water-based coating composition (2) contains a fluorine-containing polymer compound (2-1). By applying the water-based coating composition (2) to the outer periphery of the first layer to form a second layer, it is possible to form a second layer that imparts a low relative dielectric constant and a high partial discharge inception voltage to the coating layer and that, by being sufficiently adherent to the first layer, provides a coating layer with excellent interlayer strength.

The powder coating composition (2) contains a fluorine-containing polymer compound (2-2). By applying the powder coating composition (2) to the outer periphery of the first layer to form a second layer, it is possible to form a second layer that imparts a low relative dielectric constant and a high partial discharge inception voltage to the coating layer and that, by being sufficiently adherent to the first layer, provides a coating layer with excellent interlayer strength.

From the viewpoint of insulating properties, the thickness of the coating layer is preferably 30 to 200 μm, more preferably 40 μm or more, more preferably 150 μm or less, and even more preferably 100 μm or less. If the thickness is too large, it may be difficult to miniaturize the device when the coated wire is used in a motor or other device, and if the thickness is too small, sufficient insulation may not be obtained.

The thickness of the first layer is preferably 5 to 50 μm, more preferably 10 μm or more, even more preferably 15 μm or more, more preferably 40 μm or less, and even more preferably 30 μm or less, from the viewpoint of forming a coating layer that sufficiently adheres to the rectangular electric wire substrate and is resistant to wrinkles even when bent.

The thickness of the second layer is preferably 10 to 150 μm, more preferably 15 μm or more, even more preferably 20 μm or more, more preferably 100 μm or less, even more preferably less than 90 μm, and even more preferably 80 μm or less, from the viewpoint of imparting a low relative dielectric constant and a high partial discharge inception voltage to the coating layer and ensuring sufficient adhesion of the second layer to the first layer.

When the second layer is formed using the water-based coating composition (2), the thickness of the second layer can be made relatively small. In this case, the upper limit of the thickness of the second layer is preferably 50 μm or less, more preferably 40 μm or less, and even more preferably 35 μm or less.

When the second layer is formed using the powder coating composition (2), the thickness of the second layer can be made relatively large. In this case, the lower limit of the thickness of the second layer is preferably more than 35 μm, more preferably more than 40 μm, and even more preferably more than 50 μm.

The dielectric constant of the coating layer is preferably 2.1 to 2.8, and more preferably 2.6 or less. The coated electric wire of the present disclosure is an appropriate combination of the constituent materials and formation methods of the two layers, so that the dielectric constant of the coating layer can be reduced.

The partial discharge inception voltage of the coating layer is preferably 1100 to 2500 (Vp), more preferably 1200 (Vp) or more, and more preferably 2000 (Vp) or less. The coated electric wire of the present disclosure is an appropriate combination of the constituent materials and formation methods of the two layers, and therefore can increase the partial discharge inception voltage of the coating layer.

The coating layer may further include other layers as long as it includes the first layer and the second layer, but it is possible to obtain a coated electric wire that achieves the desired effect even if it does not include other layers.

(First Layer)
The first layer is formed from a water-based coating composition (1) or a powder coating composition (1).

The water-based paint composition (1) contains a polymeric compound (1) having either or both of an amide group and an imide group, and a fluorine-containing polymeric compound (1). The water-based paint composition (1) may contain only a polymeric compound (1) having either or both of an amide group and an imide group, and a fluorine-containing polymeric compound (1) as the polymeric compound.

The water-based coating composition (1) may contain water in addition to the polymer compound (1) and the fluorine-containing polymer compound (1). It is also preferable that the water-based coating composition (1) contains only water as a solvent.

From the viewpoint of easily forming a layer having the desired thickness, the viscosity of the water-based coating composition (1) is preferably 10 to 10,000 (cP), more preferably 50 (cP) or more, even more preferably 100 (cP) or more, more preferably 1,000 (cP) or less, and even more preferably 500 (cP) or less. The viscosity of the water-based coating composition (1) can be adjusted by adjusting the contents of the polymer compound (1) and the fluorine-containing polymer compound (1) in the water-based coating composition (1).

The content of the polymer compound (1) and the fluorine-containing polymer compound (1) in the water-based paint composition (1) is preferably 1 to 90% by weight, more preferably 10% by weight or more, and more preferably 80% by weight or less, based on the mass of the water-based paint composition (1).

The powder coating composition (1) contains a polymeric compound (1) having either or both of an amide group and an imide group, and a fluorine-containing polymeric compound (1). The polymeric compound (1) and the fluorine-containing polymeric compound (1) in the powder coating composition (1) are usually both in the form of powder. The powder coating composition (1) may contain only the polymeric compound (1) having either or both of an amide group and an imide group, and the fluorine-containing polymeric compound (1) as the polymeric compound.

From the viewpoint of easily forming a layer having the desired thickness, the average particle size of the powder coating composition (1) is preferably 1 to 100 (μm), more preferably 5 μm or more, even more preferably 10 μm or more, more preferably 90 μm or less, and even more preferably 80 μm or less.

In the water-based coating composition (1) or the powder coating composition (1), the volume ratio of the polymer compound (1) to the fluorine-containing polymer compound (1) is preferably 10/90 to 90/10, more preferably 15/85 or more, and more preferably 85/15 or less, from the viewpoint of sufficiently adhering the coating layer to the rectangular conductor substrate without impairing the low relative dielectric constant and high partial discharge inception voltage of the coating layer.

The aqueous coating composition (1) or the powder coating composition (1) may contain other components as necessary. Examples of other components include crosslinking agents, antistatic agents, heat stabilizers, foaming agents, foam nucleating agents, antioxidants, surfactants, photopolymerization initiators, antiwear agents, surface modifiers, various organic and inorganic pigments, copper damage inhibitors, antifoam agents, adhesion promoters, lubricants, processing aids, colorants, phosphorus stabilizers, lubricants, release agents, sliding materials, ultraviolet absorbers, dyes and pigments, reinforcing materials, drip inhibitors, fillers, curing agents, ultraviolet curing agents, and flame retardants. The content of other components in the aqueous coating composition (1) or the powder coating composition (1) is preferably less than 30% by weight, more preferably less than 10% by weight, and even more preferably 5% by weight or less, with no particular lower limit, but may be 0% by weight or more. That is, the water-based coating composition (1) or the powder coating composition (1) does not need to contain any other components.

(Second Layer)
The second layer can be formed from a water-based coating composition (2) or a powder coating composition (2).

The water-based coating composition (2) contains a fluorine-containing polymeric compound (2-1). The water-based coating composition (2) may contain only the fluorine-containing polymeric compound (2-1) as the polymeric compound.

The water-based coating composition (2) may contain water in addition to the fluorine-containing polymer compound (2-1). It is also preferable that the water-based coating composition (2) contains only water as a solvent.

From the viewpoint of easily forming a layer having the desired thickness, the viscosity of the water-based coating composition (2) is preferably 10 to 10,000 (cP), more preferably 50 (cP) or more, even more preferably 100 (cP) or more, more preferably 1,000 (cP) or less, and even more preferably 500 (cP) or less. The viscosity of the water-based coating composition (2) can be adjusted by adjusting the content of the fluorine-containing polymeric compound (2-1) in the water-based coating composition (2).

The content of the fluorine-containing polymeric compound (2-1) in the water-based coating composition (2) is preferably 1 to 90% by weight, more preferably 10% by weight or more, and more preferably 80% by weight or less, based on the mass of the water-based coating composition (2).

The powder coating composition (2) contains a fluorine-containing polymeric compound (2-2). The fluorine-containing polymeric compound (2-2) in the powder coating composition (2) is usually in the form of a powder. The powder coating composition (2) may contain only the fluorine-containing polymeric compound (2-2) as the polymeric compound.

From the viewpoint of easily forming a layer having the desired thickness, the average particle size of the powder coating composition (2) is preferably 1 to 100 (μm), more preferably 5 μm or more, even more preferably 10 μm or more, more preferably 90 μm or less, and even more preferably 80 μm or less.

The aqueous coating composition (2) or the powder coating composition (2) may contain other components as necessary. Examples of other components include crosslinking agents, antistatic agents, heat stabilizers, foaming agents, foam nucleating agents, antioxidants, surfactants, photopolymerization initiators, antiwear agents, surface modifiers, various organic and inorganic pigments, copper damage inhibitors, antifoaming agents, adhesion promoters, lubricants, processing aids, colorants, phosphorus stabilizers, lubricants, release agents, sliding materials, ultraviolet absorbers, dyes and pigments, reinforcing materials, drip prevention agents, fillers, curing agents, ultraviolet curing agents, flame retardants, and other additives. The content of other components in the aqueous coating composition (2) or the powder coating composition (2) is preferably less than 30% by weight, more preferably less than 10% by weight, and even more preferably 5% by weight or less, relative to the mass of the fluorine-containing polymer compound (2-1) or the fluorine-containing polymer compound (2-2) in the aqueous coating composition (2) or the powder coating composition (2), and may be 0% by weight or more, although the lower limit is not particularly limited. That is, the water-based coating composition (2) or the powder coating composition (2) does not need to contain any other components.

(Polymer Compound)
Next, the polymer compound used in the coating layer of the coated electric wire will be described. The polymer compound described below can be suitably used as the polymer compound (1) that forms the first layer.

In this disclosure, a "polymer compound" has either one or both of an amide group and an imide group, and preferably has no fluorine atoms. The polymer compound can have an amide group (amide bond) or an imide group (imide bond) in the main chain or side chain of the polymer compound.

As the polymer compound, from the viewpoint of adhesion to the rectangular electric wire substrate or adhesion to other layers, at least one selected from the group consisting of polyamideimide, polyetherimide, polyimide and thermoplastic polyimide is preferable, and at least one selected from the group consisting of polyamideimide and polyimide is more preferable. In addition, two or more polymer compounds can be used in combination as the polymer compound. For example, a combination of polyamideimide and polyimide can be used as the polymer compound.

Polyamide-imide is a resin made of a polymer having amide bonds and imide bonds in the molecular structure. There are no particular limitations on the polyamide-imide, and examples include a resin made of a high molecular weight polymer obtained by various reactions such as a reaction between an aromatic diamine having an amide bond in the molecule and an aromatic tetracarboxylic acid such as pyromellitic acid; a reaction between an aromatic tricarboxylic acid such as trimellitic anhydride and a diamine such as 4,4-diaminophenyl ether or a diisocyanate such as diphenylmethane diisocyanate; and a reaction between a dibasic acid having an aromatic imide ring in the molecule and a diamine. As the polyamide-imide, a polymer having an aromatic ring in the main chain is preferable.

Polyimide is a resin made of a polymer having an imide bond in its molecular structure. There are no particular limitations on the polyimide, and examples include resins made of high molecular weight polymers obtained by the reaction of aromatic tetracarboxylic anhydrides such as pyromellitic anhydride. As polyimides, those made of polymers having aromatic rings in the main chain are preferred.

(Fluorine-containing polymer compound)
Next, the fluorine-containing polymer compound used in the coating layer of the coated electric wire will be described. The fluorine-containing polymer compound described below is a fluorine-containing polymer compound (1) forming the first layer, a fluorine-containing polymer compound (2) forming the second layer, can be suitably used as the fluorine-containing polymer compound (2-1) and the fluorine-containing polymer compound (2-2) which form the following compound:

A fluorine-containing polymer compound is a polymer compound that contains fluorine atoms. A fluorine-containing polymer compound is usually a polymer compound in which the hydrogen atoms bonded to the carbon atoms that make up the main chain are partially or completely replaced with fluorine atoms.

As the fluorine-containing polymer compound, a perfluoro-based polymer compound is preferred because it provides a coating layer that exhibits a lower relative dielectric constant and a higher partial discharge inception voltage. In this disclosure, a perfluoro-based polymer compound is a polymer compound in which the content of perfluoromonomer units relative to all polymerization units constituting the polymer compound is 90 mol % or more.

In this disclosure, a perfluoromonomer is a monomer that does not contain a carbon atom-hydrogen atom bond in the molecule. In addition to carbon and fluorine atoms, a perfluoromonomer may be a monomer in which some of the fluorine atoms bonded to the carbon atoms are replaced with chlorine atoms, and may have nitrogen atoms, oxygen atoms, sulfur atoms, phosphorus atoms, boron atoms, or silicon atoms in addition to carbon atoms. A perfluoromonomer is preferably a monomer in which all hydrogen atoms are replaced with fluorine atoms.

The relative dielectric constant of the fluorine-containing polymeric compound is preferably 2.0 to 2.2, and more preferably 2.1 or less, since a coating layer exhibiting a lower relative dielectric constant and a higher partial discharge inception voltage can be obtained. The relative dielectric constant of the fluorine-containing polymeric compound can be measured in accordance with JIS-C-2138 at 23°C ± 2°C, a relative humidity of 50%, and a frequency of 1 kHz.

As the fluorine-containing polymer compound, a fluororesin is preferred. In this disclosure, a fluororesin is a partially crystalline fluoropolymer, or a fluoroplastic. A fluororesin has a melting point and is thermoplastic, but may be melt-processable or non-melt-processable.

Fluorine resins include polytetrafluoroethylene, tetrafluoroethylene (TFE)/fluoroalkyl vinyl ether (FAVE) copolymer, tetrafluoroethylene (TFE)/hexafluoropropylene (HFP) copolymer, TFE/FAVE/HFP copolymer, TFE/ethylene copolymer [ETFE], TFE/ethylene/HFP copolymer, ethylene/chlorotrifluoroethylene (CTFE) copolymer [ECTFE], polychlorotrifluoroethylene [PCTFE], CTFE/TFE copolymer, polyvinylidene fluoride [PVdF], TFE/vinylidene fluoride (VdF) copolymer [VT], polyvinyl fluoride [PVF], TFE/VdF/CTFE copolymer [VTC], and TFE/HFP/VdF copolymer.

As the fluororesin, at least one selected from the group consisting of polytetrafluoroethylene, TFE/FAVE copolymer, TFE/HFP copolymer, and TFE/FAVE/HFP copolymer is preferred.

The polytetrafluoroethylene (PTFE) may be non-melt-processable PTFE or melt-processable PTFE, with non-melt-processable PTFE being preferred.

Non-melt processable PTFE usually has extensibility, fibrillation properties, and non-melt secondary processability. Non-melt secondary processability means that the melt flow rate cannot be measured at a temperature higher than the crystallization melting point according to ASTM D 1238 and D 2116, i.e., the PTFE does not flow easily even in the melting temperature range.

PTFE may be a tetrafluoroethylene (TFE) homopolymer, or a modified PTFE containing TFE units and modified monomer units. In this disclosure, "modified PTFE" means a copolymer of TFE and a small amount of comonomer that does not impart melt processability to the resulting copolymer. The comonomer is not particularly limited, and examples thereof include hexafluoropropylene [HFP], chlorotrifluoroethylene [CTFE], and perfluoro(alkyl vinyl ether) [PAVE]. The ratio of the comonomer added to the modified PTFE varies depending on the type, but is preferably 0.001 to 1 mass% based on the total mass of TFE and the small amount of comonomer. In this disclosure, the content of each monomer unit constituting PTFE can be calculated by appropriately combining NMR, FT-IR, elemental analysis, and X-ray fluorescence analysis depending on the type of monomer.

The standard specific gravity (SSG) of PTFE is preferably 2.280 or less, more preferably 2.210 or less, even more preferably 2.200 or less, and preferably 2.130 or more. SSG can be measured by the water displacement method according to ASTM D 792 using samples molded in accordance with ASTM D 4895-89.

The peak temperature of PTFE is preferably in the range of 333 to 347°C. More preferably, it is 335°C or higher and 345°C or lower. The peak temperature is the temperature corresponding to the maximum value on the heat of fusion curve when PTFE that has not been heated to a temperature of 300°C or higher is heated at a rate of 10°C/min using a differential scanning calorimeter (DSC).

As the fluorine-containing polymer compound, a melt-processable fluorine-containing polymer compound can also be used. In particular, from the viewpoint of easily forming a layer having a desired thickness, it is preferable to use a melt-processable fluorine-containing polymer compound as the fluorine-containing polymer compound (2-2) for forming the second layer. Also, from the viewpoint of easily forming a layer having a desired thickness, it is preferable to use a melt-processable fluorine-containing polymer compound as the fluorine-containing polymer compound (1) contained in the powder coating composition (1) for forming the first layer.

In this disclosure, melt processable means that the polymer can be melted and processed using conventional processing equipment such as extruders and injection molding machines. Therefore, melt processable fluorine-containing polymer compounds typically have a melt flow rate of 0.01 to 500 g/10 min.

The melt flow rate of the fluorine-containing polymer compound is preferably 0.1 to 100 g/10 min, more preferably 80 g/10 min or less, even more preferably 70 g/10 min or less, preferably 5 g/10 min or more, more preferably 10 g/10 min or more.

The melt flow rate of a fluorine-containing polymer compound is the mass of polymer (g/10 min) flowing out of a nozzle with an inner diameter of 2.1 mm and a length of 8 mm under a load of 5 kg at 372°C using a melt indexer (manufactured by Yasuda Seiki Seisakusho Co., Ltd.) per 10 min according to ASTM D1238.

The melting point of the fluorine-containing polymer compound is preferably 200 to 322°C, more preferably 230°C or higher, even more preferably 250°C or higher, and more preferably 320°C or lower.

The melting point can be measured using a differential scanning calorimeter (DSC).

As the melt-processable fluorine-containing polymer compound, a melt-processable fluororesin is preferable. Examples of melt-processable fluororesins include tetrafluoroethylene (TFE)/fluoroalkyl vinyl ether (FAVE) copolymer, tetrafluoroethylene (TFE)/hexafluoropropylene (HFP) copolymer, TFE/FAVE/HFP copolymer, TFE/ethylene copolymer [ETFE], TFE/ethylene/HFP copolymer, ethylene/chlorotrifluoroethylene (CTFE) copolymer [ECTFE], polychlorotrifluoroethylene [PCTFE], CTFE/TFE copolymer, polyvinylidene fluoride [PVdF], TFE/vinylidene fluoride (VdF) copolymer [VT], polyvinyl fluoride [PVF], TFE/VdF/CTFE copolymer [VTC], and TFE/HFP/VdF copolymer.

As the melt-processable fluororesin, at least one selected from the group consisting of TFE/FAVE copolymer, TFE/HFP copolymer, and TFE/FAVE/HFP copolymer is preferred.

TFE/FAVE copolymer is a copolymer containing tetrafluoroethylene (TFE) units and fluoroalkyl vinyl ether (FAVE) units.

The FAVE constituting the FAVE unit is represented by the general formula (1):
CF ₂ =CFO(CF ₂ CFY ¹ O) _p - (CF ₂ CF ₂ CF ₂ O) _q - Rf (1)
(wherein ^Y1 represents F or _CF3 , Rf represents a perfluoroalkyl group having 1 to 5 carbon atoms, p represents an integer of 0 to 5, and q represents an integer of 0 to 5), and a monomer represented by general formula (2):
CFX=CXOCF ₂ OR ¹ (2)
(wherein X may be the same or different and represents H, F or _CF3 ; ^R1 represents a linear or branched fluoroalkyl group having 1 to 6 carbon atoms which may contain 1 to 2 atoms of at least one type selected from the group consisting of H, Cl, Br and I, or a cyclic fluoroalkyl group having 5 or 6 carbon atoms which may contain 1 to 2 atoms of at least one type selected from the group consisting of H, Cl, Br and I).

Among them, the FAVE is preferably a monomer represented by the general formula (1), more preferably at least one selected from the group consisting of perfluoro(methyl vinyl ether), perfluoro(ethyl vinyl ether) (PEVE) and perfluoro(propyl vinyl ether) (PPVE), even more preferably at least one selected from the group consisting of PEVE and PPVE, and particularly preferably PPVE.

The content of FAVE units in the TFE/FAVE copolymer is preferably 1.0 to 30.0 mol% relative to the total monomer units, more preferably 1.2 mol% or more, even more preferably 1.4 mol% or more, even more preferably 1.6 mol% or more, particularly preferably 1.8 mol% or more, more preferably 3.5 mol% or less, even more preferably 3.2 mol% or less, even more preferably 2.9 mol% or less, and particularly preferably 2.6 mol% or less.

The content of TFE units in the TFE/FAVE copolymer is preferably 99.0 to 70.0 mol% relative to the total monomer units, more preferably 96.5 mol% or more, even more preferably 96.8 mol% or more, even more preferably 97.1 mol% or more, particularly preferably 97.4 mol% or more, more preferably 98.8 mol% or less, even more preferably 98.6 mol% or less, even more preferably 98.4 mol% or less, and particularly preferably 98.2 mol% or less.

In the present disclosure, the content of each monomer unit in the copolymer is measured by ¹⁹ F-NMR.

The TFE/FAVE copolymer may also contain monomer units derived from monomers copolymerizable with TFE and FAVE. In this case, the content of the monomers copolymerizable with TFE and FAVE is preferably 0 to 29.0 mol%, more preferably 0.1 to 5.0 mol%, and even more preferably 0.1 to 1.0 mol%, based on the total monomer units of the TFE/FAVE copolymer.

Examples of monomers copolymerizable with TFE and FAVE include HFP, vinyl monomers represented by CZ ¹ Z ² ═CZ ³ (CF ₂ ) _n Z ⁴ (wherein Z ¹ , Z ² and Z ³ are the same or different and represent H or F, Z ⁴ represents H, F or Cl, and n represents an integer of 2 to 10), alkyl perfluorovinyl ether derivatives represented by CF ₂ ═CF-OCH ₂ -Rf ¹ (wherein Rf ¹ represents a perfluoroalkyl group having 1 to 5 carbon atoms), and monomers having functional groups. Of these, HFP is preferred.

As the TFE/FAVE copolymer, at least one selected from the group consisting of copolymers consisting only of TFE units and FAVE units, and the above-mentioned TFE/HFP/FAVE copolymers is preferred, and copolymers consisting only of TFE units and FAVE units are more preferred.

The melting point of the TFE/FAVE copolymer is preferably 280 to 322°C, more preferably 285°C or higher, more preferably 320°C or lower, and even more preferably 315°C or lower. The melting point can be measured using a differential scanning calorimeter (DSC).

The glass transition temperature (Tg) of the TFE/FAVE copolymer is preferably 70 to 110°C, more preferably 80°C or higher, and more preferably 100°C or lower. The glass transition temperature can be measured by dynamic viscoelasticity measurement.

TFE/HFP copolymer is a copolymer containing tetrafluoroethylene (TFE) units and hexafluoropropylene (HFP) units.

The content of HFP units in the TFE/HFP copolymer is preferably 0.1 to 30.0 mol % relative to the total monomer units, more preferably 0.7 mol % or more, even more preferably 1.4 mol % or more, and more preferably 10.0 mol % or less.

The content of TFE units in the TFE/HFP copolymer is preferably 70.0 to 99.9 mol%, more preferably 90.0 mol% or more, more preferably 99.3 mol% or less, and even more preferably 98.6 mol% based on the total monomer units.

The TFE/HFP copolymer may also contain monomer units derived from monomers copolymerizable with TFE and HFP. In this case, the content of the monomers copolymerizable with TFE and HFP is preferably 0 to 29.9 mol%, more preferably 0.1 to 5.0 mol%, and even more preferably 0.1 to 1.0 mol%, based on the total monomer units of the TFE/HFP copolymer.

Examples of monomers copolymerizable with TFE and HFP include FAVE, vinyl monomers represented by CZ ¹ Z ² ═CZ ³ (CF ₂ ) _n Z ⁴ (wherein Z ¹ , Z ² and Z ³ are the same or different and represent H or F, Z ⁴ represents H, F or Cl, and n represents an integer of 2 to 10), alkyl perfluorovinyl ether derivatives represented by CF ₂ ═CF-OCH ₂ -Rf ¹ (wherein Rf ¹ represents a perfluoroalkyl group having 1 to 5 carbon atoms), and monomers having functional groups. Of these, FAVE is preferred.

The melting point of the TFE/HFP copolymer is preferably 200 to 322°C, more preferably 210°C or higher, even more preferably 220°C or higher, particularly preferably 240°C or higher, more preferably 320°C or lower, even more preferably less than 300°C, and particularly preferably 280°C or lower.

The glass transition temperature (Tg) of the TFE/HFP copolymer is preferably 60 to 110°C, more preferably 65°C or higher, and more preferably 100°C or lower.

The fluorine-containing polymer compound may have a functional group.

The functional group is preferably at least one selected from the group consisting of a carbonyl group-containing group, an amino group, a hydroxy group, a _-CF2H group, an olefin group, an epoxy group, and an isocyanate group.

The carbonyl group-containing group is a group that contains a carbonyl group (-C(=O)-) in the structure. Examples of the carbonyl group-containing group include:
a carbonate group [—O—C(═O)—OR ³ (wherein R ³ is an alkyl group having 1 to 20 carbon atoms or an alkyl group having 2 to 20 carbon atoms containing an ether-bonding oxygen atom)],
An acyl group [-C(=O)-R ³ (wherein R ³ is an alkyl group having 1 to 20 carbon atoms or an alkyl group having 2 to 20 carbon atoms and containing an ether-bonding oxygen atom)]
a haloformyl group [—C(═O)X ⁵ , X ⁵ being a halogen atom];
A formyl group [—C(═O)H],
A group represented by the formula: -R ⁴ -C(═O)-R ⁵ (wherein R ⁴ is a divalent organic group having 1 to 20 carbon atoms, and R ⁵ is a monovalent organic group having 1 to 20 carbon atoms),
A group represented by the formula: -O-C(=O)-R ⁶ (wherein R ⁶ is an alkyl group having 1 to 20 carbon atoms or an alkyl group having 2 to 20 carbon atoms containing an ether-bonding oxygen atom),
Carboxyl group [-C(=O)OH],
an alkoxycarbonyl group [—C(═O)OR ⁷ (wherein R ⁷ is a monovalent organic group having 1 to 20 carbon atoms)];
a carbamoyl group [-C(=O)NR ⁸ R ⁹ (wherein R ⁸ and R ⁹ may be the same or different and are a hydrogen atom or a monovalent organic group having 1 to 20 carbon atoms)];
Acid anhydride bond [-C(=O)-OC(=O)-],
Examples include:

Specific examples of ^R3 include a methyl group, an ethyl group, a propyl group, an isopropyl group, and a butyl group. Specific examples of ^R4 include a methylene group, a _-CF2- group, and _{a -C6H4-} group, and specific examples of ^R5 include a methyl group, an ethyl group, a propyl group, an isopropyl group, and a butyl group. Specific examples of ^R7 include a methyl group, an ethyl group, a propyl group, an isopropyl group, and a butyl group. Specific examples of ^R8 and ^R9 include a hydrogen atom, a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, and a phenyl group.

A hydroxy group is a group represented by -OH or a group containing a group represented by -OH. In this disclosure, -OH constituting a carboxyl group is not included in the hydroxy group. Examples of hydroxy groups include -OH, a methylol group, and an ethylol group.

An olefin group is a group having a carbon-carbon double bond. Examples of the olefin group include those represented by the following formula:
-CR ¹⁰ =CR ¹¹ R ¹²
(wherein R ¹⁰ , R ¹¹ and R ¹² may be the same or different and are a hydrogen atom, a fluorine atom or a monovalent organic group having 1 to 20 carbon atoms), and preferably at least one selected from the group consisting of -CF═CF ₂ , -CH═CF ₂ , -CF═CHF, -CF═CH ₂ and -CH═CH ₂ .

An isocyanate group is a group represented by -N=C=O.

Functional groups can also include non-fluorinated or partially fluorinated alkyl groups, such as _-CH3 , _-CFH2 groups.

The number of functional groups in the fluorine-containing polymeric compound is preferably 5 to 2000 per ¹⁰⁶ carbon atoms. The number of functional groups per ¹⁰⁶ carbon atoms is more preferably 50 or more, even more preferably 100 or more, particularly preferably 200 or more, more preferably 1000 or less, even more preferably 800 or less, particularly preferably 700 or less, and most preferably 500 or less.

Furthermore, since a coating layer having excellent electrical properties can be formed, the number of functional groups of the fluorine-containing polymer compound may be less than 5 per ¹⁰ carbon atoms, or may be from 0 to 4. In particular, when the fluorine-containing polymer compound has melt processability, it is preferable that the number of functional groups is within the above numerical range.

The functional group is a functional group present at the main chain end or side chain end of the fluorine-containing polymer compound, and a functional group present in the main chain or side chain, preferably at the main chain end. Examples of the functional group include -CF=CF ₂ , -CF ₂ H, -COF, -COOH, -COOCH ₃ , -CONH ₂ , -OH, -CH ₂ OH, and the like, and at least one selected from the group consisting of -CF ₂ H, -COF, -COOH, -COOCH ₃ and -CH ₂ OH is preferred. -COOH includes a dicarboxylic anhydride group (-CO-O-CO-) formed by bonding two -COOH.

Infrared spectroscopy can be used to identify the types of functional groups and measure the number of functional groups.

Specifically, the number of functional groups is measured by the following method. First, the copolymer is melted at 330 to 340° C. for 30 minutes and compression molded to prepare a film having a thickness of 0.20 to 0.25 mm. This film is analyzed by Fourier transform infrared spectroscopy to obtain an infrared absorption spectrum of the copolymer, and a difference spectrum with a base spectrum in which the copolymer is completely fluorinated and no functional groups are present is obtained. From the absorption peak of a specific functional group appearing in this difference spectrum, the number of functional groups N per 1×10 ⁶ carbon atoms in the copolymer is calculated according to the following formula (A).
N=I×K/t (A)
I: absorbance K: correction coefficient t: film thickness (mm)

For reference, the absorption frequencies, molar absorption coefficients, and correction coefficients for the functional groups in this disclosure are shown in Table 1. The molar absorption coefficients were determined from FT-IR measurement data of low molecular weight model compounds.

The absorption frequencies of -CH ₂ CF ₂ H, -CH ₂ COF, -CH ₂ COOH, -CH ₂ COOCH ₃ and -CH ₂ CONH ₂ are several tens of Kaiser (cm ^-1 ) lower than the absorption frequencies of -CF ₂ H, -COF, -COOH free and -COOH bonded, -COOCH ₃ and -CONH ₂ shown in the table, respectively.
Therefore, for example, the number of functional groups of --COF is the sum of the number of functional groups determined from the absorption peak at 1883 cm.sup. ^-1 due to _--CF.sub.2 COF and the number of functional groups determined from the absorption peak at 1840 cm.sup. ^-1 due to _--CH.sub.2 COF.

The number of functional groups may be the total number of -CF=CF ₂ , -CF ₂ H, -COF, -COOH, -COOCH ₃ , -CONH ₂ and -CH ₂ OH, or may be the total number of -CF ₂ H, -COF, -COOH, -COOCH ₃ and -CH ₂ OH.

The functional group is introduced into the fluorine-containing polymer compound, for example, by a chain transfer agent or a polymerization initiator used in producing the fluorine-containing polymer compound. For example, when an alcohol is used as a chain transfer agent or a peroxide having a -CH ₂ OH structure is used as a polymerization initiator, -CH ₂ OH is introduced into the main chain end of the fluorine-containing polymer compound. Furthermore, the functional group is introduced into the side chain end of the fluorine-containing polymer compound by polymerizing a monomer having a functional group. The fluorine-containing polymer compound may contain a unit derived from a monomer having a functional group.

Examples of monomers having a functional group include cyclic hydrocarbon monomers having a dicarboxylic anhydride group (-CO-O-CO-) and a polymerizable unsaturated group in the ring, as described in JP 2006-152234 A, and monomers having functional group (f) as described in WO 2017/122743 A. Examples of monomers having a functional group include monomers having a carboxy group (maleic acid, itaconic acid, citraconic acid, undecylenic acid, etc.); monomers having an acid anhydride group (itaconic anhydride, citraconic anhydride, 5-norbornene-2,3-dicarboxylic anhydride, maleic anhydride, etc.), and monomers having a hydroxyl group or an epoxy group (hydroxybutyl vinyl ether, glycidyl vinyl ether, etc.).

The fluorine-containing polymer compound can be produced by a conventional method such as emulsion polymerization or suspension polymerization by appropriately mixing the monomers that form the constituent units of the polymer compound and additives such as a polymerization initiator.

(Method of manufacturing coated electric wire)
The coated electric wire of the present disclosure may be, for example,
A water-based coating composition (1) or a powder coating composition (1) is applied to the outer periphery of the rectangular electric wire substrate to form a first layer;
The second layer can be produced by a production method in which the water-based coating composition (2) or the powder coating composition (2) is applied to the outer periphery of the first layer to form the second layer.

The method for forming a layer by applying the water-based coating composition is not particularly limited, and examples include spray coating, roll coating, coating with a doctor blade, dip (immersion) coating, and impregnation coating.

After applying the water-based coating composition, the resulting coating film may be dried and/or baked to form a layer. Drying may be performed by a conventional method, and is preferably performed at a temperature of 60 to 200°C for 5 to 60 minutes. Baking may be performed by a conventional method, and is preferably performed at a temperature equal to or higher than the melting point or curing temperature of the polymer compound or fluorine-containing polymer compound for 5 to 60 minutes. Baking may be performed each time the coating composition is applied, or may be performed after applying the coating composition multiple times to form multiple layers (coating films).

The method for forming a layer by applying the powder coating composition is not particularly limited, and examples include electrostatic coating and fluidized bed coating.

After applying the powder coating composition, the resulting coating film may be baked to form a layer. Baking may be performed by a conventional method, but is preferably performed for 5 to 60 minutes at a temperature equal to or higher than the melting point or curing temperature of the polymer compound or fluorine-containing polymer compound. Baking may be performed each time the coating composition is applied, or may be performed after applying the coating composition multiple times to form multiple layers (coating films).

The coated electric wire of the present disclosure can be suitably used for, for example, LAN cables, USB cables, Lightning cables, HDMI cables, QSFP cables, aerospace electric wires, underground power transmission cables, submarine power cables, high voltage cables, superconducting cables, wrapped electric wires, automotive electric wires, wire harnesses and electrical equipment, robot and factory automation electric wires, office automation equipment electric wires, information equipment electric wires (optical fiber cables, LAN cables, HDMI cables, Lightning cables, audio cables, etc.), internal wiring for communication base stations, high current internal wiring (inverters, power conditioners, storage battery systems, etc.), electronic equipment internal wiring, small electronic equipment and mobile wiring, moving part wiring, electrical equipment internal wiring, measuring equipment internal wiring, power cables (for construction, wind and solar power generation, etc.), control and instrumentation wiring cables, motor cables, etc.

The coated electric wire of the present disclosure can be wound and used as a coil. The coated electric wire and coil of the present disclosure can be suitably used in electric or electronic devices such as motors, generators, and inductors. The coated electric wire and coil of the present disclosure can also be suitably used in on-vehicle electric or electronic devices such as on-vehicle motors, on-vehicle generators, and on-vehicle inductors.

Although the embodiments have been described above, it will be understood that various changes in form and details are possible without departing from the spirit and scope of the claims.

<1> According to a first aspect of the present disclosure,
A coated electric wire including a rectangular electric wire substrate and a coating layer formed on the outer periphery of the rectangular electric wire substrate,
The coating layer is
A first layer formed from a water-based coating composition (1) containing a polymeric compound (1) having either one or both of an amide group and an imide group, and a fluorine-containing polymeric compound (1), or a powder coating composition (1) containing a polymeric compound (1) having either one or both of an amide group and an imide group, and a fluorine-containing polymeric compound (1);
A second layer formed from a water-based coating composition (2) containing a fluorine-containing polymer compound (2-1) or a powder coating composition (2) containing a fluorine-containing polymer compound (2-2);
A coated electric wire comprising:
<2> According to a second aspect of the present disclosure,
According to a first aspect, there is provided a covered electric wire, in which the polymer compound (1) is at least one selected from the group consisting of polyamideimide, polyetherimide, polyimide and thermoplastic polyimide.
<3> According to a third aspect of the present disclosure,
According to the first or second aspect, there is provided a covered electric wire, wherein the fluorine-containing polymer compound (1), the fluorine-containing polymer compound (2-1) or the fluorine-containing polymer compound (2-2) is a perfluoro-based polymer compound.
<4> According to a fourth aspect of the present disclosure,
There is provided a covered electric wire according to any one of the first to third aspects, in which the relative dielectric constant of the fluorine-containing polymer compound (1), the fluorine-containing polymer compound (2-1) or the fluorine-containing polymer compound (2-2) is 2.0 to 2.2.
<5> According to a fifth aspect of the present disclosure,
There is provided a covered electric wire according to any one of the first to fourth aspects, in which the melting point of the fluorine-containing polymeric compound (2-2) is 250 to 320° C.
<6> According to a sixth aspect of the present disclosure,
There is provided a covered electric wire according to any one of the first to fifth aspects, in which a volume ratio of the polymer compound (1) to the fluorine-containing polymer compound (1) is from 10/90 to 90/10.
<7> According to a seventh aspect of the present disclosure,
There is provided a covered electric wire according to any one of the first to sixth aspects, wherein the material forming the rectangular electric wire substrate is at least one selected from the group consisting of copper, a copper alloy, aluminum and an aluminum alloy.
<8> According to an eighth aspect of the present disclosure,
There is provided a covered electric wire according to any one of the first to seventh aspects, in which the surface roughness Sz of the rectangular electric wire substrate is in the range of 0.2 to 12 μm.
<9> According to a ninth aspect of the present disclosure,
There is provided a covered electric wire according to any one of the first to eighth aspects, wherein the covering layer has a thickness of 30 to 200 μm and a relative dielectric constant of 2.1 to 2.8.
<10> According to a tenth aspect of the present disclosure,
There is provided a covered electric wire according to any one of the first to ninth aspects, in which the second layer has a thickness of 20 to 100 μm.
<11> According to an eleventh aspect of the present disclosure,
There is provided a covered electric wire according to any one of the first to tenth aspects, in which the covering layer has a partial discharge inception voltage of 1100 to 2500 (Vp).
<12> According to a twelfth aspect of the present disclosure,
There is provided a covered electric wire according to any of the first to eleventh aspects, wherein the fluorine-containing polymer compound (1), the fluorine-containing polymer compound (2-1) or the fluorine-containing polymer compound (2-2) has 5 to 1,000 functional groups per ¹⁰ carbon atoms.
<13> According to a thirteenth aspect of the present disclosure,
There is provided a covered electric wire according to any one of the first to eleventh aspects, in which the fluorine-containing polymer compound (2-2) has 0 to 4 functional groups per 10 ⁶ carbon atoms.
<14> According to a fourteenth aspect of the present disclosure,
There is provided a covered electric wire according to any one of the first to thirteenth aspects, in which the viscosity of the aqueous coating composition (2) is 10 to 10,000 (cP).
<15> According to a fifteenth aspect of the present disclosure,
There is provided a coated electric wire according to any one of the first to fourteenth aspects, in which the powder coating composition (2) has an average particle size of 1 to 100 (μm).
<16> According to a sixteenth aspect of the present disclosure,
There is provided a covered electric wire according to any one of the first to fifteenth aspects, in which a first layer is formed on an outer periphery of the rectangular electric wire substrate, and a second layer is formed on an outer periphery of the first layer.
<17> According to a seventeenth aspect of the present disclosure,
A method for producing a coated electric wire according to any one of the first to sixteenth aspects, comprising:
A water-based coating composition (1) or a powder coating composition (1) is applied to the outer periphery of the rectangular electric wire substrate to form a first layer;
A production method is provided in which a water-based coating composition (2) or a powder coating composition (2) is applied to the outer periphery of a first layer to form a second layer.
<18> According to an eighteenth aspect of the present disclosure,
According to any one of the first to sixteenth aspects, there is provided a motor including a covered electric wire.

Next, we will explain the embodiments of the present disclosure using examples, but the present disclosure is not limited to these examples.

The values in the examples were measured using the following methods.

(Surface roughness Sz)
The surface roughness Sz was measured in a visual field of ⁸⁰⁰⁰ μm2 using a laser microscope.

(Number of functional groups)
The fluorine-containing polymer compound was melted at 330 to 340°C for 30 minutes and compression molded to prepare a film having a thickness of 0.20 to 0.25 mm. This film was scanned and analyzed 40 times using a Fourier transform infrared spectrometer [FT-IR (product name: Model 1760X, manufactured by PerkinElmer) to obtain an infrared absorption spectrum, and a difference spectrum with a base spectrum in which the polymer was completely fluorinated and no functional groups were present was obtained. From the absorption peaks of specific functional groups appearing in this difference spectrum, the number N of functional groups per ¹⁰⁶ carbon atoms in the fluorine-containing polymer compound was calculated according to the following formula (A).

N=I×K/t (A)
I: absorbance K: correction coefficient t: film thickness (mm)

For reference, the absorption frequencies, molar absorption coefficients, and correction coefficients for the functional groups in this disclosure are shown in Table 2. The molar absorption coefficients were determined from FT-IR measurement data of low molecular weight model compounds.

(viscosity)
The viscosity of the water-based coating composition was measured using a B-type viscometer (BII type viscometer manufactured by Toki Sangyo Co., Ltd.) according to JIS Z8803. Rotating rotor #4 was used for the measurement. The measurement temperature was 25°C.

(Average particle size)
The average particle size of the powder coating composition was measured using a laser diffraction/scattering type particle size distribution measuring device manufactured by Nikkiso Co., Ltd. The median particle size in the volumetric particle size distribution was taken as the average particle size.

(Melt Flow Rate (MFR))
According to ASTM D1238, the mass (g/10 min) of the copolymer flowing out per 10 min from a nozzle having an inner diameter of 2.1 mm and a length of 8 mm at 372° C. under a load of 5 kg was determined using a melt indexer (manufactured by Yasuda Seiki Seisakusho).

(Melting Point)
It was determined as the temperature corresponding to the maximum value on the heat of fusion curve when the temperature was raised at a rate of 10° C./min using a differential scanning calorimeter (DSC).

(Coating thickness)
The measurement was performed using a micrometer.

(Dielectric constant)
The relative dielectric constant (ε) of the entire coating layer was calculated from the capacitance measured using an LCR HiTester 3522-50 manufactured by HIOKI Corporation, using the following formula:
C=Ca+Cb
(In the formula, C is the capacitance per unit length of the coating (pf/m), which is the combination of the capacitance of the flat portion Ca and the capacitance of the corner portion Cb.)
Ca=(ε/ε ₀ )×2×(L ₁ +L ₂ )/T
Cb=(ε/ε ₀ )×2πε ₀ /Log{(r+T)/r}/r
(In the formula, _ε0 is the dielectric constant of a vacuum, _L1 is the length of the long side of the flat portion of the rectangular electric wire substrate, _L2 is the length of the short side of the flat portion of the rectangular electric wire substrate _, T is the coating thickness of the entire electric wire, and r is the radius of curvature of the conductor corner.)

(Partial Discharge Inception Voltage (PDIV))
A test specimen was prepared by overlapping the surfaces including the long sides of the cross-sectional shape of two coated electric wires (140 mm long) over a length of 100 mm without any gap. After that, the insulating coating of 10 mm at the end of the sample was removed, and a partial discharge measuring device (DAC-PD-7 manufactured by Soken Denki Co., Ltd.) was used to apply a 50 Hz sine wave AC voltage between the rectangular electric wire substrates of the two coated electric wires in an atmosphere of 50% relative humidity. The voltage at which a discharge of 10 pC or more occurred was determined as the partial discharge inception voltage, with a voltage rise rate of 50 V/sec, a voltage drop rate of 50 V/sec, and a voltage retention time of 0 sec.

(Bending test)
A U-shaped coil was used and both sides at a point 10 mm from the base point were bent in the longitudinal direction by R2. When no wrinkles were generated in the coating layer, the coating layer was marked with an ◯, and when wrinkles were generated, the coating layer was marked with an X.

(Adhesion strength between substrate and coating layer)
The measurement was performed using an AGS-J autograph (50N) (manufactured by Shimadzu Corporation). Two strips were cut at right angles in the minor axis direction, and the ends were peeled off by 10 cm and clamped in the upper chuck. The conductor was fixed at the bottom so that the long side direction was horizontal. When the device was moved in the tensile direction, a jig that moved in conjunction with the horizontal direction according to the vertical movement distance was used, and the angle was adjusted so that the peeled off coating was always perpendicular to the conductor in the long side direction. The tensile stress was measured when pulled at 100 mm/min until 30 mm was peeled off, and the maximum point stress was taken as the adhesion strength. If the adhesion strength was 0.1 N/mm or more, it was judged to be sufficiently adhered and marked as ○. If it was less than 0.1 N/mm, it was marked as ×.

Example 1
The water-based coating composition B was applied to the outer circumference of a copper rectangular electric wire substrate having a surface roughness Sz of 0.45 μm, and then baked to form a first layer. The water-based coating composition G was further applied to the outer circumference and baked to form a second layer. The details of the method for forming the first layer using the water-based coating composition B and the method for forming the second layer using the water-based coating composition G will be described later. Various properties of the obtained coated electric wire were measured. The results are shown in Table 3.

Examples 2 to 7, Comparative Example 1
A coated electric wire was obtained in the same manner as in Example 1, except that the compositions for forming the first layer and the second layer were changed as shown in Table 3. In Comparative Example 1, the first layer was not formed. Various properties of the obtained coated electric wire were measured. The results are shown in Table 3.

Formation of the first layer using the water-based coating composition B:
Polyamideimide (PAI) varnish (resin content: 34 wt%) was poured into water to precipitate PAI. This was pulverized in a ball mill to obtain a water dispersion of PAI (solid content: 20 wt%). A water dispersion composition of PTFE (solid content: 60 wt%, functional group number: 18 per ¹⁰⁶ carbon atoms) and water were added to this to obtain a water-based coating composition B with PAI/PTFE=25/75 (volume%). The viscosity of this was 138 cP.
This water-based coating composition B was spray-coated, dried at 100° C. for 15 minutes, and then baked at 380° C. for 20 minutes to obtain a coating film having a thickness of 19 μm.

Formation of the first layer using the water-based coating composition C:
Polyimide (PI) varnish (resin content: 29 wt%) was poured into water to precipitate PI. This was pulverized in a ball mill to obtain a water dispersion of PI (solid content: 20 wt%). A water dispersion composition of PTFE (solid content: 60 wt%, functional group number: 18 per ¹⁰⁶ carbon atoms) and water were added to this to obtain a water-based coating composition C with PI/PTFE = 30/70 (volume%). The viscosity of this was 145 cP.
This water-based coating composition C was spray-coated, dried at 100° C. for 15 minutes, and then baked at 380° C. for 20 minutes to obtain a coating film having a thickness of 21 μm.

Formation of the first layer using powder coating composition E:
Polyamideimide (PAI) powder (average particle size: 20 μm) and PFA powder (TFE/PPVE copolymer, functional group number: 220 per ¹⁰⁶ carbon atoms, MFR: 27 g/10 min, melting point: 301° C., average particle size: 24 μm) were mixed to obtain a powder coating composition E with a PAI/PFA ratio of 20/80 (volume %). The average particle size was 23 μm.
This powder coating composition E was electrostatically applied and baked at 380° C. for 20 minutes to obtain a coating film having a thickness of 20 μm.

Formation of the first layer using powder coating composition F:
Polyamideimide (PAI) powder (average particle size: 20 μm) and FEP powder (TFE/HFP copolymer, functional group number: 625 per ¹⁰⁶ carbon atoms, MFR: 38 g/10 min, melting point: 258° C., average particle size: 41 μm) were mixed to obtain a powder coating composition F with PAI/FEP=20/80 (volume %). The average particle size was 26 μm.
This powder coating composition F was electrostatically applied and baked at 320° C. for 20 minutes to obtain a coating film having a thickness of 18 μm.

Formation of the second layer using the water-based coating composition G:
Water was added to a water-dispersed composition of PTFE (solid content: 60% by weight, functional group number: 18 per ¹⁰⁶ carbon atoms) to obtain a water-based coating composition G. The viscosity of this composition was 292 cP.
This water-based coating composition G was spray-coated, dried at 100° C. for 15 minutes, and then baked at 380° C. for 20 minutes to obtain a coating film having a thickness of 28 μm.

Formation of the second layer using the water-based coating composition H:
Water was added to a water-dispersed composition of PFA (solid content: 60% by weight, TFE/PPVE copolymer, functional group number: 133 per ¹⁰⁶ carbon atoms) to obtain a water-based coating composition H. The viscosity of this composition was 224 cP.
This water-based coating composition H was spray-coated, dried at 100° C. for 15 minutes, and then baked at 380° C. for 20 minutes to obtain a coating film having a thickness of 31 μm.

Formation of the second layer using powder coating composition I:
PFA powder (TFE/PPVE copolymer, functional group number: 220 per 10 ⁶ carbon atoms, MFR: 27 g/10 min, melting point: 301° C., average particle size: 24 μm) was used as powder coating composition I.
This powder coating composition I was electrostatically coated and baked at 380° C. for 20 minutes to obtain a coating film having a thickness of 47 μm.

Formation of the second layer using powder coating composition J:
PFA powder (TFE/PPVE copolymer, functional group number: 2 per 10 ⁶ carbon atoms, MFR: 28 g/10 min, melting point: 301° C., average particle size: 23 μm) was used as powder coating composition J.
This powder coating composition J was electrostatically applied and baked at 380° C. for 20 minutes to obtain a coating film having a thickness of 75 μm.

Formation of the second layer with powder coating composition K:
FEP powder (TFE/HFP copolymer, functional group number: 625 per 10 ⁶ carbon atoms, MFR: 38 g/10 min, melting point: 258° C., average particle size: 41 μm) was used as powder coating composition K.
This powder coating composition K was electrostatically applied and baked at 320° C. for 20 minutes to obtain a coating film having a thickness of 52 μm.

Claims (18)

A coated electric wire including a rectangular electric wire substrate and a coating layer formed on the outer periphery of the rectangular electric wire substrate,
The coating layer is
A first layer formed from a water-based coating composition (1) containing a polymer compound (1) having at least an imide group and a fluorine -containing polymer compound (1), or a powder coating composition (1) containing a polymer compound (1) having at least an imide group and a fluorine-containing polymer compound (1);
A second layer formed from an aqueous coating composition (2) containing only a fluorine-containing polymer compound (2-1) as a polymer compound, or a powder coating composition (2) containing only a fluorine-containing polymer compound (2-2) as a polymer compound;
A coated electric wire comprising: The coated electric wire according to claim 1, wherein the polymer compound (1) is at least one selected from the group consisting of polyamideimide, polyetherimide, polyimide, and thermoplastic polyimide. The coated electric wire according to claim 1 or 2, wherein the fluorine-containing polymer compound (1), the fluorine-containing polymer compound (2-1) or the fluorine-containing polymer compound (2-2) is a perfluoro-based polymer compound. The coated electric wire according to claim 1 or 2, wherein the relative dielectric constant of the fluorine-containing polymer compound (1), the fluorine-containing polymer compound (2-1) or the fluorine-containing polymer compound (2-2) is 2.0 to 2.2. The coated electric wire according to claim 1 or 2, wherein the melting point of the fluorine-containing polymer compound (2-2) is 250 to 320°C. The coated electric wire according to claim 1 or 2, wherein the volume ratio of the polymer compound (1) to the fluorine-containing polymer compound (1) is 10/90 to 90/10. The coated electric wire according to claim 1 or 2, wherein the material forming the rectangular electric wire substrate is at least one selected from the group consisting of copper, copper alloy, aluminum, and aluminum alloy. The coated electric wire according to claim 1 or 2, wherein the surface roughness Sz of the rectangular electric wire substrate is in the range of 0.2 to 12 μm. The coated electric wire according to claim 1 or 2, wherein the thickness of the coating layer is 30 to 200 μm, and the relative dielectric constant of the coating layer is 2.1 to 2.8. The coated electric wire according to claim 1 or 2, wherein the thickness of the second layer is 20 to 100 μm. The coated electric wire according to claim 1 or 2, wherein the partial discharge inception voltage of the coating layer is 1100 to 2500 (Vp). 3. The coated electric wire according to claim 1, wherein the fluorine-containing polymer compound (1), the fluorine-containing polymer compound (2-1) or the fluorine-containing polymer compound (2-2) has 5 to 1,000 functional groups per 10 ⁶ carbon atoms. 3. The coated electric wire according to claim 1, wherein the fluorine-containing polymer compound (2-2) has 0 to 4 functional groups per 10 ⁶ carbon atoms. The coated electric wire according to claim 1 or 2, wherein the viscosity of the water-based coating composition (2) is 10 to 10,000 (cP). The coated electric wire according to claim 1 or 2, wherein the powder coating composition (2) has an average particle size of 1 to 100 (μm). The coated electric wire according to claim 1 or 2, in which a first layer is formed on the outer periphery of the rectangular electric wire substrate, and a second layer is formed on the outer periphery of the first layer. A method for producing the coated electric wire according to claim 1 or 2, comprising the steps of:
A water-based coating composition (1) or a powder coating composition (1) is applied to the outer periphery of the rectangular electric wire substrate to form a first layer;
A production method in which a water-based coating composition (2) or a powder coating composition (2) is applied to the outer periphery of a first layer to form a second layer. A motor comprising the coated electric wire according to claim 1 or 2.