CN1477650A - Insulated conductor and insulated conductor with self-melting adhesivity - Google Patents
Insulated conductor and insulated conductor with self-melting adhesivity Download PDFInfo
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- CN1477650A CN1477650A CNA031461042A CN03146104A CN1477650A CN 1477650 A CN1477650 A CN 1477650A CN A031461042 A CNA031461042 A CN A031461042A CN 03146104 A CN03146104 A CN 03146104A CN 1477650 A CN1477650 A CN 1477650A
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/02—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of inorganic substances
- H01B3/12—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of inorganic substances ceramics
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B7/00—Insulated conductors or cables characterised by their form
- H01B7/02—Disposition of insulation
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Abstract
A ceramic insulation film 12 is formed on the circumferential surface of the wire 11 with a composition for coating containing a compound of zirconium and a compound of silicon. A primer 13 is formed on the circumferential surface of the insulation film 12 with organic resin modified silicon. A fused film 14 is formed on the circumferential surface of the primer 13 with a polyamide resin, a polyimide resin or an epoxy resin.
Description
Technical field
The present invention relates to a kind of surface and be insulated the insulated conductor that tunicle is covered, particularly a kind of self-melting adhesivity insulated conductor.
Background technology
, used at loud speaker in the past, had self-melting adhesivity, and as shown in Figure 1, on the surface of the insulation tunicle 2 of lining lead 1, formed and melting tunicle 3 for making it with the insulated conductor on sound coil and the motor coil etc.
Wherein, this insulation tunicle 2 is formed with coatings such as polyester, is that cold coating is formed and melting tunicle 3 by the pure soluble polyamide that is dissolved in the organic solvent.
Now, along with the high performance of in recent years electric machinery, for example the load of sound coil of using as loud speaker and motor coil etc. becomes bigger, and the insulated conductor for constituting aforementioned coil needs higher thermal endurance.And existing insulated conductor, its heat resisting temperature that forms the coatings such as polyester of insulation tunicle 2 is about 350 ℃, under the situation more than 350 ℃, will produce the problem of the characteristic variation of insulated conductor.
Therefore, have now, insulate tunicle and melting the new problem that tunicle is easily peeled off but then produce thus to have the method that stable on heating material forms the insulation tunicle.
Summary of the invention
Main purpose of the present invention, be for the poor heat resistance that solves existing insulated conductor and the existing insulation tunicle of self-melting adhesivity insulated conductor and insulation tunicle with melting tunicle and problem such as easily peeling off.
For reaching above-mentioned purpose, the present invention forms the insulation tunicle on the outer peripheral face of lead, and forms primary coat on the outer peripheral face of this insulation tunicle, is melting tunicle and form on the outer peripheral face of this primary coat.
The present invention forms the insulation tunicle with stable on heating material, re-uses and insulate tunicle and melting tunicle and have the well material of connecting airtight property between the two, forms primary coat at the insulation tunicle between the tunicle with melting, and has increased to insulate tunicle and melting peel strength between the tunicle.
Brief description of drawings
Below in conjunction with accompanying drawing the specific embodiment of the present invention is described in further detail.
In the accompanying drawing,
Fig. 1 is the sectional drawing of existing insulated conductor;
Fig. 2 is the stereogram of the formation of announcement insulated conductor of the present invention;
Fig. 3 is the sectional drawing of insulated conductor of the present invention;
Fig. 4 is the chemical constitution formula of the insulation tunicle of insulated conductor of the present invention;
Fig. 5 is as the chart of loud speaker with the MMP experimental data of the occasion of sound coil use with insulated conductor of the present invention;
Fig. 6 is the sectional drawing of the insulated conductor that uses with sound coil as loud speaker in the MMP experiment;
Fig. 7 is used in the cross-sectional side view of the high power loud speaker of MMP experiment with sound coil for loud speaker;
Fig. 8 is the calcspar of the MMP experimental loop of loud speaker;
Fig. 9 peels off the experimental technique key diagram of experiment for sound coil axle-coil;
Figure 10 peels off the experimental result chart of experiment for sound coil axle-coil.
Embodiment
Below, with reference to accompanying drawing, preferred forms of the present invention is described.
Fig. 2 is the state stereogram that each tunicle of an execution mode of announcement insulated conductor of the present invention strips out, and Fig. 3 is the cross-sectional view of aforementioned dielectric lead.
The diameter of lead 11 in this example, is 0.02~0.6mm.
The outer peripheral face of this insulation tunicle 12 is covered by primary coat 13, and the outer peripheral face of aforementioned primary coat 13 is being melted tunicle 14 and is being covered.
Ceramic insulation tunicle 12, be with comprise the compound of zirconium and silicon compound form the application constituent in ratio as shown in the table (weight portion), coat the outer peripheral face of lead 1 after, carry out thermmohardening, thereby form by the zirconium, the silicon that harden.
Form example 1 | Form example 2 | Form example 3 | ||
????(a) | The dimethyl-silicon resin solution | ???46 | ???60 | ???80 |
????(b-1) | Four-n-butoxy zirconium solution | ???10 | ???5 | ???8 |
????(b-2) | Tetraethoxysilane solution | ???10 | ||
????(c-1) | Dimethylbenzene | ???44 | ???10 | ???6 |
????(c-2) | Butyl glycol | ???15 | ???6 | |
Composition adds up to | ???100 | ???100 | ???100 | |
Silicon is adjusted agent | ???0.5 | ???0.5 | ||
Acetic acid | ???1.5 | ???1 |
(a) the dimethyl-silicon resin solution is 55% for its solid-state part
(b-1) four-n-butoxy zirconium solution is 31% for its solid-state part
(b-2) tetraethoxysilane solution is 42% for its solid-state part
The thickness of this ceramic insulation tunicle 12 is 3~12 μ m in this example.
Fig. 4 discloses the chemical constitution formula of this ceramic insulation tunicle 12.
Below, this ceramic insulation tunicle 12 is described.
Ceramic insulation tunicle 12, use by following (a) (b) application that constituent constituted of (c) with constituent (wherein, (a)+(b)+(c)=100 weight portion).
(a) be with general formula (R
1 2Si) n (OR
2)
2(in the formula, R
1For carbon number is 1~8 organic group, R
2For carbon number is 1~5 alkyl or is 1~4 acyl group for carbon number) selected at least a in the group of represented polysiloxane, it is scaled 5~55 weight portions with solid-state deal;
(b) be with general formula Zr (OR)
4(in the formula, R is that carbon number is 1~5 hydrocarbons residue) represented four oxyl zirconiums and four oxyl zirconiums add selected at least a zirconium compounds in the group of part condensation polymer that water decomposition thing and this add the water decomposition thing, perhaps be this zirconium compounds with general formula Si (OR)
4(in the formula, R is that carbon number is 1~5 hydrocarbons residue) represented four oxyl silane, four oxyl silane add the mixture that water decomposition thing and this add at least a silane compound selected in the group of part condensation polymer of water decomposition thing, it is scaled 0.5~15 weight portion with solid-state deal;
(c) be organic solvent, account for 30~94.5 weight portions;
This application constituent, contain for polysiloxane and have reactivity very fast, and the excellent zirconium compounds of thermal endurance, corrosion resistance and durability or the constituent of silane zirconium compounds, and make the dielectric film of high-fire resistance with flexibility, therefore can be suitable be used in above-mentioned ceramic insulation tunicle 12.
And above-mentioned composition (a) (b) also can add additives such as organic acid, inorganic acid, various interfacial agent, coupling agent, chelating and inorganic pigment in (c).
Polysiloxane in above-mentioned (a) composition is as the insulation-coated dose of use that has high-fire resistance and have flexibility.
Polysiloxane is that the water decomposition thing that adds of halogenated alkyl silane or alkoxy silane is made the dehydration material that polycondensation became, and uses the pure silicon lacquer.
It is (Si-O-Si-) to be combined into main chain with siloxanes, and have with methyl, phenyl is the silicon polymer of side chain, be in monomethyl or single trichlorosilane, to mix the material that is dissolved in the solvent to be become with the formed initial stage condensation polymer of dimethyl, diethyl or dichlorosilane, be will residue in the hydroxy in the polysiloxanes polycondensation further, thereby form the material of stereoscopic graticule ocular structure.
The methyl thermal endurance is the highest in the alkyl, and water repellency is very outstanding.
Therefore, this application mainly is to use the dimethyl-silicon resin with the polysiloxane in the constituent.
Solid-state deal in the polysiloxane in above-mentioned (a) composition is generally 45~60% (mass percents), is preferably 50~55% (mass percents).
Above-mentioned application can be 5~55 weight portions with the ratio of (a) composition in the constituent with solid-state deal conversion, and is preferably 25~50 weight portions.
When its less than 5 weight portions, be coated with lepthymenialy, and relative, (c) composition increases, thereby this is being coated with the rate deterioration, and when surpassing 55 weight portions, viscosity will excessively rise, thereby will make operability become bad, and films with blocked up and produce and break, so be not suitable for.
Four oxyl zirconiums in above-mentioned (b) composition, when having the moisture content of trace, will add water decomposition, add water decomposition four oxyl zirconiums and become, and this adds the heavily polycondensation and produce the part condensation polymer of water decomposition thing, it quantizes macromolecule, and in time through will producing film, therefore with above-mentioned (a) composition together as the high-fire resistance coating agent, and have the effect of the sclerosis of promotion above-mentioned (a) composition, densification and high heat-resistingization.
Therefore four oxyl zirconiums in above-mentioned (b) composition, it adds water decomposition and heavily polycondensation reaction is very quick, when using jointly with (a) composition, but hardens by the low-temperature heat short time.
R in the four oxyl zirconiums for example is 1~5 alkyl for carbon number, can be methyl, ethyl, n-butyl, sec-butyl, n-propyl group etc.
Can enumerate tetramethyl alcohol zirconium, tetraethoxide zirconium, four-n-butanols zirconium, four-sec-butanols zirconium and four propyl alcohol zirconiums etc. on concrete, and can use aforementioned a kind of or two or more simultaneously.
As above-mentioned (b) composition, particularly four-n-butanols zirconium is preferable.
The four oxyl zirconiums of above-mentioned (b) composition except that four oxyl zirconiums, also include it and add the heavy condensation polymer of part that water decomposition thing and this add the water decomposition thing.
This adds water decomposition thing and the heavy condensation polymer of part and can be in mixture by the material that is born in the four oxyl zirconiums, also can be the material that is cooperated in advance when mixture is adjusted.
Four oxyl silane in above-mentioned (b) composition, also can be identical with four above-mentioned oxyl zirconiums, by the existence of water and slowly add water decomposition, thereby become tetrasilane alcohol and add the water decomposition thing, this adds the water decomposition thing and produces the heavy condensation polymer of part through overweight polycondensation, thereby more macromolecule quantizes and produces film, therefore can be used as the high-fire resistance coating agent, and promotes sclerosis, densification and the high heat-resisting usefulness that turns into of (a) composition.
Four oxyl silane are compared with four oxyl zirconiums, and it adds water decomposition and heavily polycondensation reaction is very slow.
Therefore, by both are mixed, it adds the water decomposition speed appropriatenessization that will become, thereby can improve operability, and by measures such as the practicable anticrackings of adjusting hardness of film (flexibility).
R in the four oxyl silane for example is 1~5 alkyl, methyl, ethyl, n-butyl, n-propyl group or i-propyl group etc. for carbon number.
Can enumerate tetramethoxy-silicane, tetraethoxysilane, four butoxy silanes and four-n-propoxyl group silane etc. on concrete, it also can be a kind of of these materials or uses more than both simultaneously.
As above-mentioned (b) composition, be preferably tetraethoxysilane.
Four oxyl silane in above-mentioned (b) composition except that four oxyl silane, also include and add the water decomposition thing and these add the part condensation polymer of water decomposition thing.
This adds the water decomposition thing and the part condensation polymer can be in constituent, by the material of being formed in the four oxyl silane, also can use in advance to add water decomposition thing or the heavy condensation polymer of part when constituent is adjusted.
As above-mentioned (b) composition, the mixed proportion when using the mixture of four oxyl zirconiums and four oxyl silane is preferably 20~70: 30~80 weight portions, and be more preferred from 30~60: 40~70 weight portions (wherein, both add up to 100 weight portions).
Above-mentioned application is scaled 0.5~15 weight portion with the ratio of (b) composition in the constituent with solid-state deal, is preferably 1~5 weight portion.
When its less than 0.5 weight portion, its sclerous reaction will make its thermal endurance insufficient with slack-off, and when surpassing 15 weight portions, and its reaction is too fast, and will carry out excessive sclerous reaction, easily produce be full of cracks and peel off and can cause filming going up, and or not fine therefore.
Organic solvent in above-mentioned (c) composition is (a) (b) mixed dispersant and consistency adjusting agent of composition, also as aforementioned (a) (b) the setting rate adjustment agent use of composition.
For example can use low boiling point organic solvent, ethylene glycol derivative or alcohols as the organic solvent in above-mentioned (c) composition.
Specifically can enumerate dimethylbenzene, toluene, methyl ethyl ketone, ethylene glycol, vinyl acetate, ethylene glycol, single ethylether, diethylene glycol single-butyl ether, n-butyl alcohol, methyl alcohol and ethanol etc.
And can use in the aforementioned substances one or more simultaneously.
And, in the organic solvent of above-mentioned (c) composition, can include and be contained in (a) organic solvent in (b).
Above-mentioned application is 30~94.5 weight portions with the ratio of (c) composition in the constituent, is preferably 40~80 weight portions.
When less than 30 weight portions, the viscosity of constituent will uprise and make its operability become bad, and it is filmed blocked up, thereby can cause breaking.
On the one hand, when surpassing 94.5 weight portions, it is filmed thin excessively, thereby can cause realizing insulating properties, is not fine therefore.
Relevant primary coat 13 then is described.
Primary coat 13 is made of organic resin modification silicon.
This organic resin modification silicon, be that silicon lacquer and organic resin are made cold mixed cold mixing method with non-volatile part of ratio 50~90: 10~50 (adding up to 100), perhaps with organic resin and solvent after doing heating under the situation that nitrogen imports, except that desolvating and condensing water, thereby to its add with the silicon lacquer of the situation same ratio of aforementioned cold mixing method, and heated up, and after removing cohesion water, add solvent again and adjust its viscosity etc., thereby made with the method for boiling.
Aforementioned silicon lacquer is when carrying out cold mixing method, and its functional group is to use hydroxy, then uses methoxyl group and hydroxy material in the situation of the method for boiling.
As for organic resin, be to use a kind of in the resins such as epoxy radicals, acrylic, polyester-based, pure acidic group, carbamate groups and epoxide modified pure acidic group or two kinds.
In aforementioned, the silicon material of primary coat 13 and the ratio of organic resin were 50~90: 10~50 (adding up to 100), were that the ratio of 60~80: 20~40 (adding up to 100) is then preferable.
In above-mentioned, the thermal endurance that be to improve primary coat 13 is with reactive, in organic resin modification silicon material, add metal alkoxides and metal alkoxides add the water decomposition thing and this part condensation polymer that adds the water decomposition thing is also passable.
These metal alkoxides can for example be four oxyl silane, four titanium alkoxides and four oxyl zirconiums etc.
Organic resin modification silicon material can exemplify out following material.
1. polyester silicon lacquer
Non-volatile part of (%) 50
Ratio (silicon: polyester) 62: 38
Solvent xylene, propylene glycol monomethyl ether acetyl
2. acrylic acid silicon lacquer
Non-volatile part of (%) 52
(the part condensation polymers 2 of interior four titanium alkoxides)
Ratio (silicon: acrylic acid) 71: 29
Solvent xylene, n-butanols
3. epoxy silicon lacquer
Non-volatile part of (%) 50
Ratio (silicon: epoxy radicals) 55: 45
Solvent xylene, diketoalcohol
Melting tunicle 14 and be polyamide-based resin or polyimides is that resin or epoxy are that resin is dissolved the surface that the coating that is become is coated primary coat 13 with organic solvent, and is formed by the effect of curing.
This thickness that is melting tunicle 14 is 3~10 μ m in this example.
On above-mentioned insulated conductor 10, at ceramic insulation tunicle 12 and melting between the tunicle 14 and to form the reasons are as follows of primary coat 13 and state.
Just, form the zirconium silicon oxide of ceramic insulation tunicle 12, melting the polyamide-based resin of tunicle 14 or polyimides because of formation is that the connecting airtight property of resin system lacquer such as resin is very poor, so on the surface of ceramic insulation tunicle, directly form when melting tunicle, for example when insulated conductor is used as loud speaker and uses sound coil, when the high power action of loud speaker, influence because of the action of the large amplitude of loud speaker, the ceramic insulation tunicle with melting tunicle and will peel off, thereby may cause lead on the axle on the loud speaker, to come off.
And, melting tunicle for directly being formed at the lip-deep insulated conductor of ceramic insulation tunicle, it is under the environment of high temperature, because of of the influence of ceramic insulation tunicle with the pressure that is melting the gas that tunicle produces, melting tunicle and the ceramic insulation tunicle will be peeled off, thereby may cause insulated conductor to come off from for example installation sites such as axle of loud speaker.
And this insulated conductor 10 is formed by the organic resin modification silicon material that can form thermal endurance and the good high density diaphragm of anti-refrangibility because of its primary coat 13, the refrangibility in the time of therefore can guaranteeing thermal endurance and use.
The thickness of this primary coat 13 corresponding to the thermal endurance of the organic resin modification silicon material that forms this primary coat 13, is preferable with 1~5 μ m.
Again, this primary coat 13, its ceramic insulation tunicle 12 except that zirconium silicon oxide (the application constituent that comprises the compound of the compound of zirconium and silicon), by
Silicon lacquer
Four oxyl silane add the water decomposition thing
Silicon lacquer or four titanium alkoxides and four oxyl silane add water decomposition thing, molecule mixture
In above-mentioned each material, sneak into particle or fibrous powder about 3~50% various mixtures with insulating properties
When forming, also applicable etc. the ceramic-like coating material.
At the ceramic insulation tunicle 12 of insulated conductor 10 and melting the performance test that forms the insulated conductor 10 that primary coat 13 constituted between the tunicle 14 and undertaken by following each method.
(1) MMP of loud speaker experiment
Fig. 5 discloses the MMP experimental data of the loud speaker when will be at the ceramic insulation tunicle using with sound coil as loud speaker respectively with the insulated conductor that is melting the insulated conductor that is formed with primary coat between the tunicle and do not forming primary coat.
What wherein, be used in that the primary coat of the insulated conductor in this experiment uses is the polyester silicon lacquer.
This MMP experiment, as shown in Figure 6, respectively the insulated conductor with primary coat of diameter 0.25mm and the insulated conductor that does not have primary coat are wound in sound coil 20 as loud speaker that to make resistance value on the axle 21 be 3.5 ohm coil, heated 30 minutes down at 20 ℃, all oneselfs of spiral are being melted on axle 21.
This experiment is employed have the insulated conductor of primary coat and an insulated conductor that does not have primary coat melting tunicle, all use polyamide-based lacquer, and axle 21 is to be coated with to be formed with the polyimide resin material on the glass fibre cross tee.
Fig. 7 is provided with the cross-sectional side view of the loud speaker of Fig. 6 with the height output loud speaker that sound coil became for group.
This high output loud speaker 30 is being supported axle 21 by shock absorber 32 on skeleton 31, establishing oscillating plate 34 by border body 33 Jie between this axle 21 and skeleton 31.
Among Fig. 7,35 is that plate body, 36 is for blade of a sword body, 37 is magnet, by the magnetic force loop of these article formation loud speakers.
The bore of the height output loud speaker in this example is 17cm.
Fig. 8 is that the height of Fig. 7 is exported the calcspar of the experimental loop of loud speaker.
In this Fig. 8, produce pink noise by pink noise oscillator NG, and in pink noise, produce the experiment frequency characteristic by weighting network WN (IEC268-1C standard), drive and height is exported loud speaker 30 via wave absorption loop CL and amplifier A.
Then, obtain its power value with virtual value type potentiometer V instrumentation voltage.
The MMP experiment is exported loud speaker 30 with experiment beginning input wattage with height and is driven one minute, had a rest two minutes thereafter, pattern repeats ten times according to this, obtain temperature from loud speaker with the resistance value of sound coil 20 at each time point, and the mode of input wattage with each rising 10W repeated to test, till loud speaker is destroyed with sound coil 20.
This MMP result of experiment, as shown in Figure 5, be used in loud speaker have on sound coil 20 insulated conductor of primary coat occasion (the represented person of O) its use the occasion (the represented person of Δ) of the insulated conductor that does not have primary coat, significantly, loud speaker uses the broken string temperature of sound coil 20 than higher.
And in this MMP experiment, in the end, the tunicle that melting of polyamide-based lacquer is melted by heat and loud speaker is come off on axle 21 with sound coil 20, and this loud speaker breaks because of contacting plate body 34 or blade of a sword body 35 with sound coil 20.
Yet at this loud speaker during with sound coil 20 broken strings, the ceramic insulation tunicle does not also melt and keeps the lining state of lead, and keeps its insulation property.
(2) fabric strip separating experiment
The order coating after heat hardening, is carried out the experiment of peeling off of using fabric strip with zirconium silicon oxide coatings, primary coat and polyamide-based lacquer on copper coin.
Simultaneously, as a comparative example, after order coating on the copper coin is with zirconium silicon oxide coatings and polyamide-based lacquer and heat hardening, carry out the experiment of peeling off of using fabric strip.
The heating-up temperature of its each tunicle and time and thickness are as follows.
Heating-up temperature/time: 250 ℃/30 minutes (zirconium silicon oxide coatings)
200 ℃/30 minutes (primary coat and polyamide-based lacquer)
Thickness: 5 μ m (each coating is common)
This peels off result of experiment, and the tunicle that forms primary coat is not peeled off on fabric strip, and the tunicle that does not form primary coat then adheres to the formed tunicle of polyamide-based lacquer and produces and peel off on fabric strip.
(3) sound coil axle-coil is peeled off experiment
For using zirconium silicon oxide to use polyamide-based lacquer as the ceramic insulation tunicle,, measure the peel strength of melting tunicle respectively in occasion that forms primary coat and the occasion that does not form primary coat as the ceramic insulation lead that is melting tunicle.
Wherein, use the polyester silicon lacquer as primary coat.
Its experimental technique such as following.
It is wide with the ceramic insulation lining lead 5mm of line footpath 0.15mm at first to reel on the polyimides axle cylindraceous of diameter 20mm, thereby forms two layers spiral, with 200 ℃ of heating 30 minutes, all one of spiral is being melted on axle.
As shown in Figure 9, axle 40 and spiral 41 together along its axis cut into half after, spiral 41 along the tangential direction of axle 40 towards with its a coiling direction opposite side peeled off thereafter.
The measurement result of the peel strength of this moment as shown in figure 10.
Be formed with the ceramic insulation lead of primary coat in Figure 10 as can be known, than the ceramic insulation lead that does not form primary coat, its peel strength improves 50% approximately.
Peel off after experiment ends at this, it is destroyed to melt tunicle on the ceramic insulation lead that forms primary coat, and in the occasion of the ceramic insulation lead that does not form primary coat, produces on ceramic insulation tunicle and the interface of melting tunicle and peels off.
As the example of above-mentioned enforcement kenel according to insulated conductor of the present invention, form the insulation tunicle and form primary coat and be its upperseat concept in the enforcement kenel of the insulated conductor of outer peripheral face formation the melting tunicle of primary coat at the outer peripheral face of this insulation tunicle with outer peripheral face at lead.
This upperseat concept is implemented the insulated conductor in the kenel, for example its insulation tunicle is to form with zirconium silicon oxide, and melting tunicle is the formed situation of lacquer type organic coating with polyamide-based resin or polyimides, when mutual the connecting airtight property of insulation tunicle and each formation material that is melting tunicle is good, by with the material that has good connecting airtight property between the two, form primary coat at the insulation tunicle between the tunicle with melting, can increase and insulate tunicle and melting peel strength between the tunicle.
Whereby, above-mentioned insulated conductor and self-melting adhesivity insulated conductor, the occasion of using with sound coil as loud speaker at this insulated conductor etc. for example, large amplitude action in the time of can preventing because of the action of the high power of loud speaker etc. makes the insulation tunicle and is melting tunicle and peel off, thereby avoids lead to take place from situations such as the axle of loud speaker come off.
Claims (9)
1, a kind of insulated conductor is characterized in that: form the insulation tunicle at the outer peripheral face of lead, and form primary coat at the outer peripheral face of this insulation tunicle, melting tunicle and form at the outer peripheral face of this primary coat.
2, insulated conductor according to claim 1 is characterized in that: the aforementioned dielectric tunicle is formed with constituent by the application that comprises zirconium compounds and silicon compound.
3, insulated conductor according to claim 1 is characterized in that: the aforementioned dielectric tunicle be silicon lacquer or four oxyl silane add adding water decomposition thing or molecule mixture or in aforementioned substances, sneaking into particle respectively or mixture that fibrous powder 3~50% is become of water decomposition thing, silicon lacquer or four titanium alkoxides and four oxyl silane with insulating properties.
4, insulated conductor according to claim 1 is characterized in that: aforementioned primary coat is formed by organic resin modification silicon.
5, insulated conductor according to claim 4 is characterized in that: add in the aforementioned organic resin modification silicon metal alkoxides, metal alkoxides add the water decomposition thing, this adds in the part condensation polymer of water decomposition thing one or more.
6, insulated conductor according to claim 5 is characterized in that: aforementioned metal alkoxides is one or more the metal in four oxyl silane, four titanium alkoxides, the four oxyl zirconiums.
7, insulated conductor according to claim 1, it is characterized in that: the aforementioned tunicle that melting is carried out to cure again after being coated with caking property coating on the side face outside the formed primary coat on the outer peripheral face of insulation tunicle and is formed, and this caking property coating for by organic solvent dissolution polyamide-based resin or polyimides be that resin or epoxy resin are formed.
8, insulated conductor according to claim 1 is characterized in that: it is used in loud speaker with on the sound coil.
9, insulated conductor according to claim 1 is characterized in that: described insulated conductor has self-melting adhesivity.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2002212246A JP4021720B2 (en) | 2002-07-22 | 2002-07-22 | Insulated conductors and self-bonding insulated conductors |
JP212246/2002 | 2002-07-22 |
Publications (2)
Publication Number | Publication Date |
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CN1477650A true CN1477650A (en) | 2004-02-25 |
CN1312704C CN1312704C (en) | 2007-04-25 |
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Application Number | Title | Priority Date | Filing Date |
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CNB031461042A Expired - Fee Related CN1312704C (en) | 2002-07-22 | 2003-07-22 | Insulated conductor and insulated conductor with self-melting adhesivity |
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JP (1) | JP4021720B2 (en) |
KR (1) | KR20040030238A (en) |
CN (1) | CN1312704C (en) |
TW (1) | TWI259476B (en) |
Cited By (1)
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CN111627592A (en) * | 2020-07-01 | 2020-09-04 | 西比里电机技术(苏州)有限公司 | High-temperature-resistant corona-resistant ceramic film covered wire and preparation method thereof |
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US6872565B2 (en) * | 2003-01-29 | 2005-03-29 | Biogaia Ab | Product containing Lactobacillus reuteri strain ATTC PTA-4965 or PTA-4964 for inhibiting bacteria causing dental caries |
TWI459408B (en) * | 2010-04-27 | 2014-11-01 | Totoku Electric | Insulated wires and coils |
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US4978813A (en) * | 1989-08-29 | 1990-12-18 | W. L. Gore & Associates, Inc. | Electrical cable |
EP0772206A3 (en) * | 1995-11-02 | 2000-01-19 | Mitsubishi Cable Industries, Ltd. | Flat cable and fabrication thereof |
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2002
- 2002-07-22 JP JP2002212246A patent/JP4021720B2/en not_active Expired - Fee Related
-
2003
- 2003-07-21 KR KR1020030049797A patent/KR20040030238A/en not_active Application Discontinuation
- 2003-07-22 CN CNB031461042A patent/CN1312704C/en not_active Expired - Fee Related
- 2003-07-22 TW TW092120013A patent/TWI259476B/en not_active IP Right Cessation
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111627592A (en) * | 2020-07-01 | 2020-09-04 | 西比里电机技术(苏州)有限公司 | High-temperature-resistant corona-resistant ceramic film covered wire and preparation method thereof |
CN114678159A (en) * | 2020-07-01 | 2022-06-28 | 西比里电机技术(苏州)有限公司 | High-temperature-resistant and corona-resistant ceramic-organic insulating composite wire and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
KR20040030238A (en) | 2004-04-09 |
TW200404310A (en) | 2004-03-16 |
JP4021720B2 (en) | 2007-12-12 |
CN1312704C (en) | 2007-04-25 |
TWI259476B (en) | 2006-08-01 |
JP2004055377A (en) | 2004-02-19 |
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