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CN107936556A - A kind of black matt Kapton preparation method - Google Patents

A kind of black matt Kapton preparation method Download PDF

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Publication number
CN107936556A
CN107936556A CN201711352478.0A CN201711352478A CN107936556A CN 107936556 A CN107936556 A CN 107936556A CN 201711352478 A CN201711352478 A CN 201711352478A CN 107936556 A CN107936556 A CN 107936556A
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black
polyamic acid
resin solution
kapton
acid resin
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Inventor
任小龙
韩艳霞
黄孙息
周福龙
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Guilin Electrical Equipment Scientific Research Institute Co Ltd
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Guilin Electrical Equipment Scientific Research Institute Co Ltd
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    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/18Manufacture of films or sheets
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/10Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
    • C08G73/1003Preparatory processes
    • C08G73/1007Preparatory processes from tetracarboxylic acids or derivatives and diamines
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    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/10Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
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    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/10Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
    • C08G73/1067Wholly aromatic polyimides, i.e. having both tetracarboxylic and diamino moieties aromatically bound
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    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
    • C08G73/06Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
    • C08G73/10Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
    • C08G73/1067Wholly aromatic polyimides, i.e. having both tetracarboxylic and diamino moieties aromatically bound
    • C08G73/1071Wholly aromatic polyimides containing oxygen in the form of ether bonds in the main chain
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    • C08J2379/00Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen, or carbon only, not provided for in groups C08J2361/00 - C08J2377/00
    • C08J2379/04Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
    • C08J2379/08Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
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    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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    • C08J2479/00Characterised by the use of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen, or carbon only, not provided for in groups C08J2461/00 - C08J2477/00
    • C08J2479/04Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
    • C08J2479/08Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
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    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
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    • C08K5/18Amines; Quaternary ammonium compounds with aromatically bound amino groups

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Abstract

The present invention is a kind of black matt Kapton preparation method, key step:Ith, polyamic acid resin solution is routinely prepared.IIth, black paste is prepared, black pigment amount is 2~20wt% of polyamic acid resin solution solid content M.IIIth, black polyamic acid resin solution, polyamic acid resin solution and black paste blending and stirring are prepared, defoaming is spare.IVth, the salivation of black polyamic acid solution carries out the high temperature surface treatment that a temperature is 300 DEG C~400 DEG C, the time is 5s~90s in steel band when dry;Stretched afterwards, imidization and sizing, black matt Kapton is made.Also the delustring agent dispersing liquid for 2~20wt% that delustring dosage is M can be added in step III.The black pigment and delustering agent average grain diameter of the present invention is moderate, increases high temperature surface treatment in resin solution salivates forming process, gained film light transmittance, glossiness and physico mechanical characteristic have clear improvement.

Description

A kind of black matt Kapton preparation method
Technical field
The present invention relates to Kapton manufacturing technology, is specially a kind of black matt Kapton preparation side Method.
Background technology
Flexible printed wiring board (FPC) is widely used in 3C Product, optical lens module, liquid crystal display (LCD) module And the product such as solar cell, and Kapton (Polyimide Film, abbreviation PI film) is commonly used for its base material or covering Membrane material, since traditional PI film is respectively provided with high surface flatness in application process, film surface reflects most incident ray And produce high gloss.The dazzle or astigmatism that the film surface of high gloss is produced there are light reflection, cause the uncomfortable of vision, when long Between watch when easily make eye fatigue.Especially there is the high gloss PI films polyamides Asia of the colors such as black, white, blueness, red Amine film, influence of the reflected light that its surface produces to vision are more notable.
On the other hand, when the larger and transparent higher PI films of surface gloss are applied to FPC, the circuit design point of FPC Cloth is easy to understand and plagiarized by the same trade.
So the existing market demand possesses the PI films of the characteristics such as low-luster, low light transmission and high insulation resistance.Low-luster The high insulation resistance and low light transmission of black PI films can protect internal circuit design, while component facade can be made to have more texture and U.S. See.
The production technology of Kapton is using the polyamic acid resin solution by polycondensation reaction synthesis as original at present Material, on slobbering machine salivation obtain the polyamic acid thick film with self-supporting, then by heating stretching, imidization, sizing at Reason obtains Kapton.Obtain having concurrently the Kapton of low-luster, low light transmission and high insulation resistance, poly- Must be added in imide membrane preparation process in colour additive (such as:Colorant, dyestuff etc.) and delustering agent.General technique is Colour additive is used to reduce the light transmittance of Kapton, or addition delustering agent causes Kapton surface shape Into concave-convex micro-structure to reduce the glossiness of Kapton.
The delustering agent of micron-level particle size is generally used in the prior art, because of the filtration system filter core aperture of existing extrusion die Smaller, delustering agent frequently results in filtration system and blocks during extrusion salivates, and can not realize the serialization film of long period. If the foreign matters such as the impurity that increase filtration system filter core aperture is be easy to cause in resin solution, gel are embedded in film again, cause thin Film surface quality declines.
In black polyamide thin film manufacturing process, when inorganic particle (delustering agent) or carbon powder material (being in colour additive) Particle diameter is too big or too small, and or adding too much or it is too low can be caused for the physical property of Kapton it is undesirable Influence.If the particle diameter of inorganic particle or carbon powder material is larger, manufactured film surface is excessively coarse, is not suitable for electronic product In;If the particle diameter of inorganic particle or carbon powder material is smaller, powder clustering phenomena is easily produced, causes additive in film to disperse Non-uniform problem, and the operation of manufacturing process is difficult to control.It is dispersed in Kapton to influence additive, removes The particle diameter of inorganic particle or carbon powder material, also has the content of inorganic particle or carbon powder material.If in film inorganic particle or The content of carbon powder material is very few, and film glossiness and light transmittance can not just reduce and reach requirement.And content it is larger when, can equally produce Raw additive disperses non-uniform problem;A large amount of addition delustering agents also result in Kapton performance degradation, easy embrittlement, And a large amount of additives easily occur sedimentation and reunite in polyamic acid resin, can also increase the production cost of film.
The material of delustering agent can be divided into inorganic compound and organic compound.Wherein inorganic compound includes silica, oxygen Change aluminium, calcium carbonate, barium sulfate, titanium dioxide etc., inorganic particulate has higher bulk density, if adding substantial amounts of inorganic particulate It is may result in polyimide matrix to reunite and disperse inequality, so that the uniformity of film electrical insulating property is reduced, it is unfavorable In subsequent applications.And the organic compound for being used for delustering agent includes poly- carbonic acid vinegar (PC), polystyrene (PS), polymethylacrylic acid Methyl esters (PMMA), polyethylene (PE), polypropylene (PP), two vinegar of poly terephthalic acid second (PET), epoxy resin etc..Due to poly- In the preparation process of imide membrane, chemical conversion temperature must be more than 250 DEG C, but above-mentioned organic compound can not all bear 250 DEG C or higher temperature.Made an addition to when using such organic compound as delustering agent in Kapton, film can occur Crackle or hole, or because melt it is uneven produce color inconsistent patch the defects of.
At present, the main production technology of delustring black PI films is divided into two classes:One kind is to add black pigment in PI resins With delustering agent filler, then there is the PI films of low-transmittance and low-luster by chemical imidization or hot imidization, synthesis, This method is easy to operate, and positive effect, but due to the addition of mass filler, significantly reduces the mechanical property of PI films Energy;Another kind of is one layer of PI film containing black pigment and photoextinction of coating on the single or double of PI basement membranes.Although this Kind method can preferably make Kapton that desirable black effect be presented, and can ensure that Kapton is certain Mechanical performance, but the black resin being additionally coated with would generally increase manufacturing process and cost, and to Kapton Matter adversely affects.In addition, also Kapton can be caused to be exposed to hot adverse circumstance because resin coated layer heat resistance is poor When performance degradation easily occurs.Existing many patent applications in relation to manufacturing low gloss black polyamide thin film, but because of manufacture Complex process, production control accuracy requirement is higher and manufactures the defects such as cost height, it is difficult to implements.
Such as Chinese invention patent CN104742461A " the double-deck polyimide films and its system of low-luster of application in 2015 Make method " blending is inserted between levels polyimide film there is black pigment and form recess and hole in the thickness direction of film The polyimide film in hole, obtains having high screening optical activity, the double-deck Kapton of low-luster concurrently.The China of application in 2015 Patent of invention CN 104830058A " polyimide film of low-k and low-luster and preparation method thereof ", film main structure It is monofilm or multilayer for the fluoro containing polymers of polyimides, the carbon black of 0.5wt% to 5wt% and 15wt% to 40wt% Film.Chinese invention patent " delustering agent, the polyimides containing the delustering agent being made of polyimides powder of application in 2012 Film and preparation method thereof " is disclosed the organic matting agent that polyimides powder is formed being uniformly distributed in Kapton and made The Kapton of good film characteristics and low-luster must be had concurrently.The Chinese invention patent CN of application in 2012 103561953A " polyimide film " on the single or double of the polyimide layer (A) containing black organic pigment have comprising Inorganic or organic filler polyimide layer (B), electrical insulating property, the electricity of the film are excellent in reliability.
The content of the invention
The purpose of the present invention is design a kind of black matt Kapton preparation method, polyamic acid resin solution stream Saliva form a film when, during dry solidification, before or after high-temperature region increase high temperature surface treatment, then carry out biaxial tension, High temperature imidization and heat treatment.Kapton product glossiness obtained by this law and light transmittance substantially reduce, film roll Profile pattern increase, appearance substantially improve.
A kind of black matt Kapton preparation method provided by the invention, including following key step:
Ith, the preparation of polyamic acid resin solution
Prepare polyamic acid resin solution according to a conventional method, in an inert atmosphere, control synthetic system temperature for 12 DEG C~ Aromatic diamine is added into solvent under conditions of 75 DEG C and be stirred dissolving, after aromatic diamine is completely dissolved, divide 3~8 times at the uniform velocity It is (0.9~1.1) to add with aromatic diamine molar ratio:1 aromatic dianhydride, and stirred with 120r/ minutes~1200r/ minutes, Synthesize to obtain polyamic acid resin solution through 3~24h of polycondensation reaction.
In view of cost, inert atmosphere is generally realized with nitrogen.
The solvent is aprotic polar solvent low molecular weight Carboxylamide, specially N, N'- dimethylacetylamides (DMAC), N, N'- dimethylformamide (DMF), 1-methyl-2-pyrrolidinone (NMP), dimethyl sulfoxide (DMSO), tetramethyl sulfone, N, N'- dimethyl-N, N'- acrylic urea (DMPU), N, any one in N dialkyl group Carboxylamides or any a variety of combination.
The polyamic acid resin solution that the dosage control of the aromatic diamine, aromatic dianhydride and solvent is formed for this step In the ratio of solid content M be 10wt%~50wt%.
The aromatic diamine is 3,4'- diaminodiphenyl ethers, 1,3- bis--(4- amino-benzene oxygens) benzene, 4,4'- diaminourea two Phenylate (4,4'-ODA), 1,3- diaminobenzenes, 2,2'- bis- (trifluoromethyl) benzidine, 4,4'- benzidines and p-phenylenediamine (p-PDA) any one in or any a variety of combination.
The aromatic dianhydride is Pyromellitic Acid diacid (PMDA), 3,3', and 4,4'- biphenyl four completes acid diacid acid anhydride (BPDA), 2,2', 3,3'- biphenyl four completes acid diacid acid anhydride (BPDA), diphenyl ether tetraformic dicarboxylic anhydride (ODPA), Benzophenone and completes acid two Double (the 3,4- dicarboxylic acids phenyl) hexafluoropropane dianhydrides (6FDA) of acid anhydrides (BTDA), 2,2-, the double phthalic anhydrides of 4,4'- oxygen (ODPA), 3,4,3', 4'- diphenyl thio-ether tetrformate dianhydride (3,4,3', 4'-TDPA), 2,3,2', 3'- diphenyl thio-ether tetrformates It is any one in dianhydride (2,3,2', 3'-TDPA) and 2,3,3', 4'- diphenyl thio-ether tetrformate dianhydride (2,3,3', 4'-TDPA) Kind or any a variety of combination.
IIth, prepared by black paste
Take black pigment to add in solvent to be mixed evenly to obtain black paste;The amount for adding black pigment is step I 2wt%~20wt% of solid content M in the polyamic acid resin solution, 0.01~0.8 μ of black pigment average grain diameter m。
The solvent is aprotic polar solvent low molecular weight Carboxylamide, specially N, N'- dimethylacetylamides (DMAC), N, N'- dimethylformamide (DMF), 1-methyl-2-pyrrolidinone (NMP), dimethyl sulfoxide (DMSO), tetramethyl sulfone, N, N'- dimethyl-N, N'- acrylic urea (DMPU), N, any one in N dialkyl group Carboxylamides or any a variety of combination.
The solvent dosage control of the black paste be black pigment content ratio in black paste be 10wt%~ 30wt%.
The amount of the black pigment added is preferably 6wt%~10wt% of M.
The average grain diameter for the black pigment that preferred version is added for O.015 μm~0.4 μm, be preferably average grain diameter O.02 μm~0.1 μm.If the particle diameter of black pigment is smaller, the phenomenon of aggregation is easily produced, causes to disperse non-uniform ask in the film Topic, and be difficult to control in process operations.If the particle diameter of black pigment is larger, manufactured film surface is excessively coarse, does not apply to In electronic product;If the additive amount of filler is too small, the same light-proofness effect that suppresses reduces;If excessive, polyamides Asia is damaged Amine film physical property.
The mixing after black pigment is added in the solvent first to mix shear agitation, afterwards high speed dispersion mulser Emulsification pretreatment processing, then handled through high pressure homogenizing, black paste is made.
IIIth, prepared by black polyamic acid resin solution
Polyamic acid resin solution obtained by step I, black paste blending and stirring obtained by step II are taken, black polyamide is made Acid resin solution, and defoam spare;
IVth, prepared by black matt Kapton
Black polyamic acid solution prepared by step III is coated on ring steel belt by extrusion molding mould, and thickness 20~ 520 μm, then for ring steel belt by baking oven, dry solidification removes the solvent of 85wt%~40wt% at 100~250 DEG C, obtains To with can self-supporting polyamide acid film.The ring steel belt of black polyamic acid solution is coated with the high temperature by baking oven Before or after area, the high temperature surface treatment that a temperature is 300 DEG C~400 DEG C, the duration is 5s~90s is also carried out.
By gained have can the polyamide acid film of self-supporting peeled off from ring steel belt and be delivered to biaxial tension in length and breadth 0.8~2.2 times of stretching is carried out on machine, 180 DEG C~500 DEG C high temperature imidization processing, after last 180 DEG C~360 DEG C sizings, are received Volume, is made the black matt Kapton of 2.5~50 μm of thickness.
The high temperature surface treatment, makes the black pigment inside film carry out surface migration, wriggling and uniformly aggregation occurs, Filler is coarse by self assembly behavior generation (micron order) and irregular molding modified surface, reduces film glossiness.It is if high Temperature is too low during temperature surface treatment, extinction effect unobvious;Temperature is excessive, be easy to cause film degradation, and film physical property reduces; High temperature is surface-treated the time too short same unobvious of its extinction effect, and processing time is long, be easy to cause film degradation, film Physical property reduces.
Preferred version is that the temperature of the high temperature surface treatment is 320 DEG C~380 DEG C, and the time is 10s~60s.
Preferred solution is that the temperature of the high temperature surface treatment is 330 DEG C~350 DEG C, and the time is 15s~30s.
The temperature of the present invention increased high temperature surface treatment in slobbering machine baking oven is far above salivation high-temperature region at present most 250 DEG C of high-temperature, TRANSIENT HIGH TEMPERATURE are to reduce the specially treated technique of film surface glossiness.
The step III can also add delustring agent dispersing liquid when preparing black polyamic acid resin solution.The step III is made During standby black polyamic acid resin solution, take polyamic acid resin solution obtained by step I, black paste obtained by step II and disappear Photo etching dispersion liquid blending and stirring, is made black polyamic acid resin solution, and defoams spare.
Preparing for the delustring agent dispersing liquid is as follows:
Cancel after photo etching is added in solvent and be mixed evenly to obtain delustring agent dispersing liquid, the delustring dosage of addition is step 2wt%~20wt% of solid content M in the I polyamic acid resin solution, the delustering agent average grain diameter are 0.01~0.8 μm。
The solvent is aprotic polar solvent low molecular weight Carboxylamide, specially N, N'- dimethylacetylamides (DMAC), N, N'- dimethylformamide (DMF), 1-methyl-2-pyrrolidinone (NMP), dimethyl sulfoxide (DMSO), tetramethyl sulfone, N, N'- dimethyl-N, N'- acrylic urea (DMPU), N, any one in N dialkyl group Carboxylamides or any a variety of combination.
The delustering agent is any one in silica, polyimides, aluminium oxide and titanium dioxide or any a variety of Combination.
The solvent dosage control of the delustring agent dispersing liquid is that the dulling agent content ratio in delustring agent dispersing liquid is 10wt%~30wt%.
Preferred version is 8wt%~12wt% that the amount of the delustering agent added is M.
The delustering agent average grain diameter that preferred version is added for O.05 μm~0.6 μm, the delustering agent preferably added is averaged Particle diameter O.08 μm~0.3 μm.
If the average grain diameter of delustering agent is too small relative to Kapton thickness to be prepared, suppress glossiness effect Reduce;If excessive, can not be sufficiently secured within Kapton.It is same to suppress gloss if the additive amount of filler is too small Spending effect reduces;If excessive, Kapton physical property is damaged.
The mixing added in the solvent after delustering agent is mixing shear agitation to be first, afterwards high speed dispersion mulser Emulsification pretreatment processing, then ground machine milled processed, and further carry out ultrasonic disperse processing and delustring agent dispersing liquid is made.
The step I prepares polyamic acid resin solution, step II prepares black paste and prepares delustring agent dispersing liquid Solvent used is identical.
Compared with prior art, it is the advantages of a kind of black matt Kapton preparation method of the invention:1st, film It is surface-treated by short time high temperature, black pigment is reunited, reduces film surface glossiness;High temperature surface treatment also eliminates film Striated surface and stress in thin films, hence it is evident that improve Kapton product surface quality;2nd, the black matt prepared by this law Kapton visible light transmittance rate is less than 0.1%, 60 ° of gloss value < 25, elongation > 60%, and tensile strength >= 230MPa, elastic modulus G T.GT.GT 3.5GPa, and maintain the insulation performance and mechanical property of Kapton itself;3rd, it is prepared Black matt Kapton has shading, photoextinction, and because the processing on high temperature surface enhances the tear resistance of film Energy;4th, the increased high temperature process of surface treatment of institute, can be in the baking oven of the existing slobbering machine in Kapton manufacturing process Interior to increase high temperature section to realize, debugging is easy, and can ensure that producing continuous, technique is simple and convenient to operate;5th, the present invention also may be used Delustering agent is added with up to more preferably extinction effect, and conventional delustering agent particle diameter is micron order, delustering agent granularity of the invention is only 0.01~0.8 μm, favorably ensure film-insulated performance and mechanical property;6th, the black matt polyimides prepared by this method is thin Film is suitable for basement membrane or cover layer, electronic tag basement membrane of flexible print circuit board etc..
Embodiment
Embodiment 1
Ith, the preparation of polyamic acid resin solution
In nitrogen atmosphere, synthetic system temperature is controlled as 12 DEG C, to 45kg N, N'- dimethylacetylamides (DMAC) solvent Middle addition 2.39kg aromatic diamines 4,4'- diaminodiphenyl ethers (4,4'-ODA) are stirred dissolving, and 4,4'-ODA are completely dissolved Afterwards, it is 1 to divide 8 at the uniform velocity addition and aromatic diamine molar ratios:1 2.61kg aromatic dianhydride Pyromellitic Acid diacid (PMDA), And stirred with 1200r/ minutes, synthesize to obtain solid content M=5kg through polycondensation reaction 12h, i.e. solid content ratio is the poly- of 10wt% Amic acid resin solution;
IIth, prepared by black paste
The 20wt% of the solid content M in polyamic acid resin solution as obtained by step I takes carbon black 1kg to add solvent N, It is mixed evenly to obtain the black paste of content of carbon black 30% in N'- dimethylacetylamides (DMAC) 2.33kg;This example carbon black 0.01 μm of average grain diameter.
The black pigment of this step can also use black titanium, bone black (bone black), Cyanine Black (cyanine black), second Acetylene black, lampblack, graphite, iron oxide black, nigrosine and Hua Jing it is black in any one or any a variety of combination.
The mixing added in this example N, N'- dimethylacetylamide (DMAC) solvent after black pigment carbon black exists to be first Shear agitation 30 minutes is mixed under the conditions of 120r/ minutes, after through high speed dispersion mulser emulsification pretreatment processing in 3600r/ minute 240 minutes, then through the high-pressure homogeneous processing of high pressure homogenizer 180MPa 30 minutes, black paste is made.
Also prepare delustring agent dispersing liquid.
The 2wt% of the solid content M in polyamic acid resin solution as obtained by step I cancels photo etching silica 0.1kg It is mixed evenly to obtain dioxide-containing silica ratio 20% after adding in solvent N, N'- dimethylacetylamide (DMAC) 0.5kg Delustring agent dispersing liquid, this example silica average grain diameter be 0.8 μm.
The delustering agent of this step can also use any one in polyimides, aluminium oxide and titanium dioxide or any a variety of Combination.
The mixing added in this example solvent N, N'- dimethylacetylamide (DMAC) after delustering agent silica exists to be first Shear agitation 30 minutes is mixed under the conditions of 1200r/ minutes, after through high speed dispersion mulser emulsification pretreatment processing in 1200r/ minute 30 minutes, then ground machine milled processed 30 minutes, and further carry out that delustering agent point is made after ultrasonic disperse is handled 240 minutes Dispersion liquid.
IIIth, prepared by black polyamic acid resin solution
Polyamic acid resin solution obtained by step I, black paste and delustring agent dispersing liquid blending and stirring obtained by step II are taken, Black polyamic acid resin solution is made, and defoams spare.
IVth, prepared by black matt Kapton
Black polyamic acid solution prepared by step IV is coated on ring steel belt by extrusion molding mould, 20 μ of thickness M, then ring steel belt is by baking oven, and dry solidification removes the solvent of 40wt% at 100 DEG C, obtains with can self-supporting Polyamide acid film.This example is coated with the ring steel belt of black polyamic acid solution before the high-temperature region by baking oven, to its into The high temperature surface treatment that temperature of row is 300 DEG C, the duration is 5s.
By gained have can the polyamide acid film of self-supporting peeled off from ring steel belt and be delivered to biaxial tension in length and breadth 2.2 times of stretchings, 500 DEG C of high temperature imidizations processing are carried out on machine, then after carrying out 360 DEG C of sizings, winding, is made 2.5 μm of thickness Black matt Kapton.
Embodiment 2
Ith, the preparation of polyamic acid resin solution
In nitrogen atmosphere, to control synthetic system temperature be 75 DEG C, to 45kg N, in N'- dimethylformamides (DMF) solvent 2.39kg aromatic diamines 4 are added, 4'- diaminodiphenyl ethers (4,4'-ODA) are stirred dissolving, after 4,4'-ODA are completely dissolved, It is 1 to divide 8 at the uniform velocity addition and aromatic diamine molar ratios:1 2.61kg aromatic dianhydride Pyromellitic Acid diacid (PMDA), and with Stir within 1200r/ minutes, synthesize to obtain solid content M=5kg through polycondensation reaction 12h, i.e. solid content ratio is the polyamide of 10wt% Acid resin solution;
IIth, prepared by black paste
The 20wt% of the solid content M in polyamic acid resin solution as obtained by step I takes bone black 1kg to add solvent N, It is mixed evenly to obtain the black paste of bone black content 18% in N'- dimethylformamides (DMF) 4.56kg;This example bone black is put down Equal 0.08 μm of particle diameter.
The mixing added in this example N, N'- dimethylformamide (DMF) solvent after black pigment carbon black exists to be first Shear agitation 60 minutes is mixed under the conditions of 200r/ minutes, after through high speed dispersion mulser emulsification pretreatment processing in 2800r/ minute 240 minutes, then through the high-pressure homogeneous processing of high pressure homogenizer 120MPa 45 minutes, black paste is made.
IIIth, prepared by black polyamic acid resin solution
Polyamic acid resin solution obtained by step I, black paste blending and stirring obtained by step II are taken, black polyamide is made Acid resin solution, and defoam spare.
IVth, prepared by black matt Kapton
Black polyamic acid solution prepared by step III is coated on ring steel belt by extrusion molding mould, 50 μ of thickness M, then ring steel belt is by baking oven, and dry solidification removes the solvent of 50wt% at 120 DEG C, obtains with can self-supporting Polyamide acid film.This example is coated with the ring steel belt of black polyamic acid solution after the high-temperature region by baking oven, to its into The high temperature surface treatment that temperature of row is 320 DEG C, the duration is 10s.
By gained have can the polyamide acid film of self-supporting peeled off from ring steel belt and be delivered to biaxial tension in length and breadth 1.8 times of stretchings, 480 DEG C of high temperature imidizations processing are carried out on machine, then after carrying out 320 DEG C of sizings, winding, is made the black of 5 μm of thickness Color delustring Kapton.
Embodiment 3
Ith, the preparation of polyamic acid resin solution
In nitrogen atmosphere, to control synthetic system temperature be 22 DEG C, to 37.5kg N, in N'- dialkyl group Carboxylamide solvents Add 6.38kg aromatic diamines 2, double (trifluoromethyl) benzidine of 2'- are stirred dissolving, after it is completely dissolved, divide 3 times it is even It is 0.98 that speed, which is added with aromatic diamine molar ratio,:1 5.99kg aromatic dianhydrides 3,3', 4,4'- biphenyl four completes acid diacid acid anhydride (BPDA), and with 1000r/ minutes stir, synthesize to obtain solid content M=12.4kg through polycondensation reaction 8h, i.e. solid content ratio is The polyamic acid resin solution of 25wt%;
IIth, prepared by black paste
The 16wt% of the solid content M in polyamic acid resin solution as obtained by step I takes iron black 2kg to add solvent N, It is mixed evenly to obtain the black paste of iron black content 10% in N'- diformazan first sulfoxide (DMSO) 18kg;This example is iron black average 0.8 μm of particle diameter.
The mixing added in this example solvent after black pigment is similar to Example 1.
IIIth, prepared by black polyamic acid resin solution
Polyamic acid resin solution obtained by step I, black paste blending and stirring obtained by step II are taken, black polyamide is made Acid resin solution, and defoam spare.
IVth, prepared by black matt Kapton
Black polyamic acid solution prepared by step III is coated on ring steel belt by extrusion molding mould, 75 μ of thickness M, then ring steel belt is by baking oven, and dry solidification removes the solvent of 50wt% at 120 DEG C, obtains with can self-supporting Polyamide acid film.This example is coated with the ring steel belt of black polyamic acid solution before the high-temperature region by baking oven, to its into The high temperature surface treatment that temperature of row is 400 DEG C, the duration is 90s.
By gained have can the polyamide acid film of self-supporting peeled off from ring steel belt and be delivered to biaxial tension in length and breadth 1.2 times of stretchings, 380 DEG C of high temperature imidizations processing are carried out on machine, then after carrying out 300 DEG C of sizings, winding, is made 7.5 μm of thickness Black matt Kapton.
Embodiment 4
Ith, the preparation of polyamic acid resin solution
In nitrogen atmosphere, to control synthetic system temperature be 40 DEG C, to 37.5kg N, in N'- dialkyl group Carboxylamide solvents Add 6.38kg aromatic diamines 2, double (trifluoromethyl) benzidine of 2'- are stirred dissolving, after it is completely dissolved, divide 6 times it is even It is 0.98 that speed, which is added with aromatic diamine molar ratio,:1 5.99kg aromatic dianhydrides 3,3', 4,4'- biphenyl four completes acid diacid acid anhydride (BPDA), and with 1000r/ minutes stir, synthesize to obtain solid content M=12.4kg through polycondensation reaction 8h, i.e. solid content ratio is The polyamic acid resin solution of 25wt%;
IIth, prepared by black paste
The 16wt% of the solid content M in polyamic acid resin solution as obtained by step I takes lampblack 2kg to add solvent N, It is mixed evenly to obtain the black paste of lampblack content 10% in N'- diformazan first sulfoxide (DMSO) 8kg;This example lampblack is averaged grain 0.8 μm of footpath.
The mixing added in this example solvent after black pigment is similar to Example 1.
And prepare delustring agent dispersing liquid.
The 20wt% of the solid content M in polyamic acid resin solution as obtained by step I cancels photo etching silica 2.5kg It is mixed evenly to obtain disappearing for dioxide-containing silica ratio 30% after adding in solvent N-methyl pyrilidone (NMP) 5.8kg Photo etching dispersion liquid, this example silica average grain diameter are 0.01 μm.
The mixing added in this example solvent after delustering agent is similar to Example 1.
IIIth, prepared by black polyamic acid resin solution
Preparing for this step black polyamic acid resin solution is same as Example 1.
IVth, prepared by black matt Kapton
Black polyamic acid solution prepared by step III is coated on ring steel belt by extrusion molding mould, 520 μ of thickness M, then ring steel belt is by baking oven, and dry solidification removes the solvent of 85wt% at 250 DEG C, obtains with can self-supporting Polyamide acid film.This example is coated with the ring steel belt of black polyamic acid solution after the high-temperature region by baking oven, to its into The high temperature surface treatment that temperature of row is 380 DEG C, the duration is 60s.
By gained have can the polyamide acid film of self-supporting peeled off from ring steel belt and be delivered to biaxial tension in length and breadth 0.8 times of stretching, 180 DEG C of high temperature imidizations processing are carried out on machine, then after carrying out 180 DEG C of sizings, winding, is made the black of 50 μm of thickness Color delustring Kapton.
Embodiment 5
Ith, the preparation of polyamic acid resin solution
In nitrogen atmosphere, synthetic system temperature is controlled to add for 50 DEG C into 25kg 1-methyl-2-pyrrolidinones (NMP) solvent Enter 7.92kg aromatic diamines 3,4'- diaminodiphenyl ethers (3,4'-ODA) are stirred dissolving, after it is completely dissolved, divide 5 times It is 1.02 at the uniform velocity to add with aromatic diamine molar ratio:1 17.23kg aromatic dianhydrides 2, double (3, the 4- dicarboxylic acids phenyl) hexafluoros of 2- Propane dianhydride (6FDA), and stirred with 1000r/ minutes, synthesize to obtain solid content M=25.15kg through polycondensation reaction 8h, i.e., contain admittedly Amount ratio is the polyamic acid resin solution of 50wt%;
IIth, prepared by black paste
The 4wt% of the solid content M in polyamic acid resin solution as obtained by step I takes acetylene black 1kg to add solvent N- It is mixed evenly to obtain the black paste of acetylene black content 15% in methyl pyrrolidone (NMP) 5.6kg;This example acetylene black is put down Equal 0.02 μm of particle diameter.
The mixing added in this example solvent after black pigment is similar to Example 1.
It is prepared by delustring agent dispersing liquid
The 16wt% of the solid content M in polyamic acid resin solution as obtained by step I cancels photo etching aluminium oxide 4.04kg It is mixed evenly to obtain the delustering agent of alumina content ratio 20% after adding in solvent N-methyl pyrilidone (NMP) 16kg Dispersion liquid, this example aluminium oxide average grain diameter are 0.3 μm.
The mixing added in this example solvent after delustering agent is similar to Example 1.
IIIth, prepared by black polyamic acid resin solution
Preparing for this step black polyamic acid resin solution is same as Example 1.
IVth, prepared by black matt Kapton
Black polyamic acid solution prepared by step III is coated on ring steel belt by extrusion molding mould, 250 μ of thickness M, then ring steel belt is by baking oven, and dry solidification removes the solvent of 70wt% at 180 DEG C, obtains with can self-supporting Polyamide acid film.This example is coated with the ring steel belt of black polyamic acid solution before the high-temperature region by baking oven, to its into The high temperature surface treatment that temperature of row is 350 DEG C, the duration is 30s.
By gained have can the polyamide acid film of self-supporting peeled off from ring steel belt and be delivered to biaxial tension in length and breadth 1.2 times of stretchings, 380 DEG C of high temperature imidizations processing are carried out on machine, then after carrying out 250 DEG C of sizings, winding, is made the black of 25 μm of thickness Color delustring Kapton.
Embodiment 6
Ith, the preparation of polyamic acid resin solution
In argon gas atmosphere, synthetic system temperature is controlled as 60 DEG C, to 42.5kg N, N'- dimethyl-N, N'- acrylic urea (DMPU) 2.22kg aromatic diamines p-phenylenediamine (p-PDA) is added in solvent and is stirred dissolving, after p-PDA is completely dissolved, divide 8 Secondary at the uniform velocity add with aromatic diamine molar ratio is 1.1:1 5.48kg aromatic dianhydrides biphenyl four completes acid diacid acid anhydride (BPDA), and Stirred with 800r/ minutes, synthesize to obtain solid content M=7.7kg through polycondensation reaction 3h, i.e. solid content ratio is the polyamides of 15wt% Amino acid resin solution;
IIth, prepared by black paste
The 6wt% of the solid content M in polyamic acid resin solution as obtained by step I takes the black 0.47kg of titanium to add solvent N, It is mixed evenly to obtain the black paste of the black content 10% of titanium in N'- dialkyl group Carboxylamides 4.23kg;This example titanium is black average 0.1 μm of particle diameter.
The mixing added in this example solvent after black pigment is similar to Example 1.
Also prepare delustring agent dispersing liquid.
The 5wt% of the solid content M in polyamic acid resin solution as obtained by step I takes TITANIUM DIOXIDE DELUSTRANT 0.39kg It is mixed evenly to obtain disappearing for dioxide-containing silica ratio 12% after adding in solvent N, N'- dialkyl group Carboxylamide 2.86kg Photo etching dispersion liquid, this example titanium dioxide average grain diameter are 0.08 μm.
The mixing added in this example solvent after delustering agent is similar to Example 1.
IIIth, prepared by black polyamic acid resin solution
Preparing for this step black polyamic acid resin solution is same as Example 1.
IVth, prepared by black matt Kapton
Black polyamic acid solution prepared by step III is coated on ring steel belt by extrusion molding mould, 360 μ of thickness M, then ring steel belt is by baking oven, and dry solidification removes the solvent of 60wt% at 150 DEG C, obtains with can self-supporting Polyamide acid film.This example is coated with the ring steel belt of black polyamic acid solution before the high-temperature region by baking oven, to its into The high temperature surface treatment that temperature of row is 330 DEG C, the duration is 30s.
By gained have can the polyamide acid film of self-supporting peeled off from ring steel belt and be delivered to biaxial tension in length and breadth 1.6 times of stretchings, 450 DEG C of high temperature imidizations processing are carried out on machine, then after carrying out 300 DEG C of sizings, winding, is made the black of 36 μm of thickness Color delustring Kapton.
Embodiment 7
Ith, the preparation of polyamic acid resin solution
In argon gas atmosphere, control synthetic system temperature to be 15 DEG C, to 40kg N, add in N'- Dimethyl Asian Maple (DMSO) solvent Enter 2.49kg aromatic diamines p-phenylenediamine (p-PDA) and be stirred dissolving, after it is completely dissolved, point 4 at the uniform velocity additions and virtue Race's diamines molar ratio is 1:1 7.51kg 3,4,3', 4'- diphenyl thio-ether tetrformates dianhydride (3,4,3', 4'-TDPA), and with Stir within 800r/ minutes, synthesize to obtain solid content M=10kg through polycondensation reaction 8h, i.e. solid content ratio is the polyamide of 20wt% Acid resin solution;
IIth, prepared by black paste
The 2wt% of the solid content M in polyamic acid resin solution as obtained by step I takes nigrosine 0.2kg to add solvent In N, N'- dimethyl-N, N'- acrylic urea (DMPU) 0.64kg, it is mixed evenly to obtain the black of nigrosine content 30% Slurry;0.4 μm of this example carbon black average grain diameter.
The mixing added in this example solvent after black pigment is similar to Example 1.
Also prepare delustring agent dispersing liquid.
The 8wt% of the solid content M in polyamic acid resin solution as obtained by step I takes TITANIUM DIOXIDE DELUSTRANT 0.8kg It is mixed evenly to obtain content of titanium dioxide ratio 30% after adding in solvent N, N'- dimethylformamide (DMF) 1.86kg Delustring agent dispersing liquid, this example titanium dioxide average grain diameter be 0.05 μm.
The mixing added in this example solvent after delustering agent is similar to Example 1.
IIIth, prepared by black polyamic acid resin solution
Preparing for this step black polyamic acid resin solution is same as Example 1.
IVth, prepared by black matt Kapton
Black polyamic acid solution prepared by step III is coated on ring steel belt by extrusion molding mould, 400 μ of thickness M, then ring steel belt is by baking oven, and dry solidification removes the solvent of 50wt% at 200 DEG C, obtains with can self-supporting Polyamide acid film.This example is coated with the ring steel belt of black polyamic acid solution after the high-temperature region by baking oven, to its into The high temperature surface treatment that temperature of row is 380 DEG C, the duration is 60s.
By gained have can the polyamide acid film of self-supporting peeled off from ring steel belt and be delivered to biaxial tension in length and breadth 1 times of stretching, 250 DEG C of high temperature imidizations processing are carried out on machine, then after carrying out 220 DEG C of sizings, winding, is made the black of 40 μm of thickness Delustring Kapton.
Embodiment 8
Ith, the preparation of polyamic acid resin solution
In argon gas atmosphere, synthetic system temperature is controlled as 72 DEG C, to 40kg N, N'- dimethylacetylamides (DMAC) solvent Middle addition 4.79kg aromatic diamines 4,4'- diaminodiphenyl ethers (4,4'-ODA) are stirred dissolving, and 4,4'-ODA are completely dissolved Afterwards, it is 1 to divide 8 at the uniform velocity addition and aromatic diamine molar ratios:1 5.21kg aromatic dianhydride Pyromellitic Acid diacid (PMDA), And stirred with 800r/ minutes, synthesize to obtain solid content M=10kg through polycondensation reaction 12h, i.e. solid content ratio is the poly- of 20wt% Amic acid resin solution;
IIth, prepared by black paste
The 10wt% of the solid content M in polyamic acid resin solution as obtained by step I takes graphite 1kg to add solvent N, It is mixed evenly to obtain the black paste of content of graphite 30% in N'- dimethylacetylamides (DMAC) 2.33kg;This example graphite 0.015 μm of average grain diameter.
The mixing added in this example solvent after black pigment is similar to Example 1.
Also prepare delustring agent dispersing liquid.
The 12wt% of the solid content M in polyamic acid resin solution as obtained by step I cancels photo etching polyimides 1.2kg It is mixed evenly to obtain polyimide content ratio 30% after adding in solvent N, N'- dimethylacetylamide (DMAC) 2.8kg Delustring agent dispersing liquid, this example polyimides average grain diameter be 0.6 μm.
The mixing added in this example solvent after delustering agent is similar to Example 1.
IIIth, prepared by black polyamic acid resin solution
Preparing for this step black polyamic acid resin solution is same as Example 1.
IVth, prepared by black matt Kapton
Black polyamic acid solution prepared by step III is coated on ring steel belt by extrusion molding mould, 100 μ of thickness M, then ring steel belt is by baking oven, and dry solidification removes the solvent of 80wt% at 220 DEG C, obtains with can self-supporting Polyamide acid film.This example is coated with the ring steel belt of black polyamic acid solution before the high-temperature region by baking oven, to its into The high temperature surface treatment that temperature of row is 340 DEG C, the duration is 15s.
By gained have can the polyamide acid film of self-supporting peeled off from ring steel belt and be delivered to biaxial tension in length and breadth 2 times of stretchings, 300 DEG C of high temperature imidizations processing are carried out on machine, then after carrying out 260 DEG C of heat treatments, winding, is made 10 μm of thickness Black matt Kapton.
Comparative example is 1.
Step I to III same as Example 1,
When prepared by step IV black matt Kapton, the surface treatment of no high temperature, only according to conventional filming technology into Black matt Kapton is made in row coating, dry solidification, stretching, imidization, heat treatment.
Comparative example is 2.
Step I to III same as Example 2,
When prepared by step IV black matt Kapton, the surface treatment of no high temperature, only according to conventional filming technology into Black matt Kapton is made in row coating, dry solidification, stretching, imidization, heat treatment.
Comparative example is 3.
Step I, III and step IV are same as Example 1, and preparing for step II black paste is same as Example 1.
When prepared by step II delustring agent dispersing liquid, the average grain diameter of delustering agent silica is 2 μm, more than 1 μm.Still by step The 2wt% of solid content M in the polyamic acid resin solution of rapid I gained takes 0.1kg silica to add solvent N, N'- dimethyl It is mixed evenly to obtain the delustring agent dispersing liquid of dioxide-containing silica ratio 20% after in acetamide (DMAC) 0.5kg.
Comparative example is 4.
Step I, III and step IV are same as Example 1, and preparing for step II black paste is same as Example 1.
When prepared by step II delustring agent dispersing liquid, the average grain diameter of delustering agent silica is 0.008 μm, less than 0.01 μ m。
Comparative example is 5.
Step I, III and step IV are same as Example 1, preparation and 1 phase of embodiment of step II delustring agent dispersing liquid Together.
When prepared by step II black paste, 1.8 μm of carbon black average grain diameter, the black pigment more than application claims is averaged grain 0.8 μm of the footpath upper limit.
Other preparation methods are identical with 1 step II of embodiment.
Comparative example is 6.
Step I, III and step IV are same as Example 1, preparation and 1 phase of embodiment of step II delustring agent dispersing liquid Together.
When prepared by step II black paste, 0.008 μm of carbon black average grain diameter, the black pigment less than application claims is averaged 0.01 μm of particle diameter limit.
Comparative example is 7.
Step I to III same as Example 1,
When prepared by step IV black matt Kapton, exist in the ring steel belt for being coated with black polyamic acid solution It is surface-treated by carrying out the high temperature that a temperature is 500 DEG C, the duration is 120s after the high-temperature region of baking oven to it.This step Rapid other processes are identical with 1 step IV of embodiment.
Comparative example is 8.
Step I to III same as Example 1,
When prepared by step IV black matt Kapton, exist in the ring steel belt for being coated with black polyamic acid solution It is surface-treated by carrying out the high temperature that a temperature is 260 DEG C, the duration is 20s after the high-temperature region of baking oven to it.This step Rapid other processes are identical with 1 step IV of embodiment.
It is swollen to detect the light transmittance of black polyamide thin film made from the various embodiments described above and each comparative example, glossiness, heat Swollen coefficient (CTE), tensile strength, elongation, modulus, tearing strength and show the performances such as quality, the results are shown in Table 1:
1 embodiment of the present invention of table and the performance table of comparisons of film obtained by comparative example
As shown in table 1, embodiment 1 to 8 prepare black matt Kapton have relatively low glossiness, thoroughly The excellent optical property such as light rate and mechanical property (tensile strength, elongation and modulus are of a relatively high), while also show height Resistance to tearing (tearing strength) and good thermal property (such as CTE, shrinking percentage is relatively low).
1., 2. the black polyamide of middle preparation is thin for comparative example without high temperature surface treatment in polyamide acid film drying process Film does not have desired optical property, thermal property and mechanical property.Comparative example used black pigment or disappears 3. in 6. The average grain diameter of photo etching is excessive or too small, and the black polyamide thin film optical property of preparation, thermal property and mechanical property are bright It is aobvious poor.Comparative example 7. in, the high temperature of polyamic acid resin dry solidification process surface treatment temperature is excessive, causes polyamic acid Resin fragmentation can not continuous film forming.Comparative example 8. in, high temperature during polyamide acid film dry solidification surface treatment temperature mistake Low, the filler reunion unobvious such as film surface delustering agent, black pigment, cause film glossiness still higher.
Above-described embodiment, is only further described the purpose of the present invention, technical solution and beneficial effect specific A example, the present invention are not limited to this.All any modifications made within the scope of disclosure of the invention, equivalent substitution, change Into etc., it is all contained within protection scope of the present invention.

Claims (10)

1. a kind of black matt Kapton preparation method, including following key step:
Ith, the preparation of polyamic acid resin solution
Polyamic acid resin solution is prepared according to a conventional method, and in an inert atmosphere, it is 12 DEG C~75 DEG C to control synthetic system temperature Under conditions of add aromatic diamine into solvent and be stirred dissolving, after aromatic diamine is completely dissolved, divides and at the uniform velocity add for 3~8 times It is (0.9~1.1) with aromatic diamine molar ratio:1 aromatic dianhydride, and stirred with 120r/ minutes~1200r/ minutes, through contracting 3~24h of poly- reaction synthesizes to obtain polyamic acid resin solution;
The solvent is aprotic polar solvent low molecular weight Carboxylamide, specially N, N'- dimethylacetylamides, N, N'- Dimethylformamide, 1-methyl-2-pyrrolidinone, dimethyl sulfoxide, tetramethyl sulfone, N, N'- dimethyl-N, N'- acrylic urea, N, N bis- Any one in alkyl carboxyl acid amides or any a variety of combination;
In the polyamic acid resin solution that the dosage control of the aromatic diamine, aromatic dianhydride and solvent is formed for this step The ratio of solid content M is 10wt%~50wt%;
The aromatic diamine is 3,4'- diaminodiphenyl ethers, 1,3- bis--(4- amino-benzene oxygens) benzene, 4,4'- diaminourea hexichol Any one in ether, 1,3- diaminobenzenes, 2,2'- bis- (trifluoromethyl) benzidine, 4,4'- benzidines and p-phenylenediamine Or any a variety of combination;
The aromatic dianhydride is Pyromellitic Acid diacid, 3,3', and 4,4'- biphenyl four completes acid diacid acid anhydride, 2,2', 3,3'- biphenyl Four, which complete acid diacid acid anhydride, diphenyl ether tetraformic dicarboxylic anhydride, Benzophenone, completes double (the 3,4- dicarboxylic acids phenyl) hexafluoros third of acid diacid acid anhydride, 2,2- Alkane dianhydride, 4,4'- oxygen double phthalic anhydride, 3,4,3', 4'- diphenyl thio-ether tetrformates dianhydride, 2,3,2', 3'- diphenyl sulfides Any one in tetracarboxylic acid dianhydride and 2,3,3', 4'- diphenyl thio-ether tetrformate dianhydride or any a variety of combination;
IIth, prepared by black paste
Take black pigment to add in solvent to be mixed evenly to obtain black paste;The amount of black pigment is added as described in step I 2wt%~20wt% of solid content M in polyamic acid resin solution, 0.01~0.8 μm of the black pigment average grain diameter;
The solvent is aprotic polar solvent low molecular weight Carboxylamide, specially N, N'- dimethylacetylamides, N, N'- Dimethylformamide, 1-methyl-2-pyrrolidinone, dimethyl sulfoxide, tetramethyl sulfone, N, N'- dimethyl-N, N'- acrylic urea, N, N bis- Any one in alkyl carboxyl acid amides or any a variety of combination;
The solvent dosage control of the black paste is that the black pigment content ratio in black paste is 10wt%~30wt%;
IIIth, prepared by black polyamic acid resin solution
Polyamic acid resin solution obtained by step I, black paste blending and stirring obtained by step II are taken, black polyamic acid tree is made Lipoprotein solution, and defoam spare;
IVth, prepared by black matt Kapton
Black polyamic acid solution prepared by step III is coated on ring steel belt by extrusion molding mould, and 20 μm of thickness~ 520 μm, then for ring steel belt by baking oven, dry solidification removes the solvent of 85wt%~40wt% at 100~250 DEG C, obtains To with can self-supporting polyamide acid film;The ring steel belt of black polyamic acid solution is coated with the high temperature by baking oven Before or after area, the high temperature surface treatment that a temperature is 300 DEG C~400 DEG C, the duration is 5s~90s is also carried out;
By gained have can the polyamide acid film of self-supporting peel off and be delivered in length and breadth on biaxial orientation stretching machine from ring steel belt 0.8~2.2 times of stretching is carried out, 180 DEG C~500 DEG C high temperature imidization processing, after last 180 DEG C~360 DEG C sizings, wind, system Obtain the black matt Kapton of 2.5 μm~50 μm of thickness.
2. black matt Kapton preparation method according to claim 1, it is characterised in that:
The temperature that the step IV prepares the high temperature surface treatment during black matt Kapton is 320 DEG C~380 DEG C, the time is 10s~60s.
3. black matt Kapton preparation method according to claim 1, it is characterised in that:
The temperature that the step IV prepares the high temperature surface treatment during black matt Kapton is 330 DEG C~350 DEG C, the time is 15s~30s.
4. black matt Kapton preparation method according to claim 1, it is characterised in that:
The amount that the black pigment that black paste is added is prepared in the step II is 6wt%~10wt% of M.
5. black matt Kapton preparation method according to claim 1, it is characterised in that:
Prepared in the step II average grain diameter of the black pigment that black paste is added O.02 μm~0.1 μm.
6. black matt Kapton preparation method according to any one of claim 1 to 5, it is characterised in that:
The step III is additionally added delustring agent dispersing liquid when preparing black polyamic acid resin solution;Take polyamide obtained by step I Black paste and delustring agent dispersing liquid blending and stirring obtained by acid resin solution, step II, it is molten to be made black polyamic acid resin Liquid, and defoam spare;
Preparing for the delustring agent dispersing liquid is as follows:
Cancel after photo etching is added in solvent and be mixed evenly to obtain delustring agent dispersing liquid, the delustring dosage of addition is step I institute 2wt%~20wt% of the solid content M in polyamic acid resin solution is stated, the delustering agent average grain diameter is 0.01 μm~0.8 μ m;
The solvent is aprotic polar solvent low molecular weight Carboxylamide, specially N, N'- dimethylacetylamides, N, N'- Dimethylformamide, 1-methyl-2-pyrrolidinone, dimethyl sulfoxide, tetramethyl sulfone, N, N'- dimethyl-N, N'- acrylic urea, N, N bis- Any one in alkyl carboxyl acid amides or any a variety of combination;
The delustering agent is any one or any a variety of group in silica, polyimides, aluminium oxide and titanium dioxide Close;
The solvent dosage control of the delustring agent dispersing liquid be dulling agent content ratio in delustring agent dispersing liquid be 10wt%~ 30wt%.
7. black matt Kapton preparation method according to claim 6, it is characterised in that:
The amount for the delustering agent that the delustring agent dispersing liquid is added when preparing is 8wt%~12wt% of M.
8. black matt Kapton preparation method according to claim 6, it is characterised in that:
The average grain diameter for the delustering agent that the delustring agent dispersing liquid is added when preparing for O.05 μm~0.6 μm.
9. black matt Kapton preparation method according to claim 6, it is characterised in that:
The average grain diameter for the delustering agent that the delustring agent dispersing liquid is added when preparing for O.08 μm~0.3 μm.
10. black matt Kapton preparation method according to claim 6, it is characterised in that:
The step I prepares polyamic acid resin solution, step II prepares black paste and prepares used in delustring agent dispersing liquid Solvent it is identical.
CN201711352478.0A 2017-12-15 2017-12-15 A kind of black matt Kapton preparation method Pending CN107936556A (en)

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CN114230830A (en) * 2022-01-12 2022-03-25 江西冠德新材科技股份有限公司 Easily degradable glue-free matte film and preparation method thereof

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