CN106571233B - A kind of processing method for improving capacitor surface corrosion resistance - Google Patents
A kind of processing method for improving capacitor surface corrosion resistance Download PDFInfo
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- CN106571233B CN106571233B CN201610944224.7A CN201610944224A CN106571233B CN 106571233 B CN106571233 B CN 106571233B CN 201610944224 A CN201610944224 A CN 201610944224A CN 106571233 B CN106571233 B CN 106571233B
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- stainless steel
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- 239000003990 capacitor Substances 0.000 title claims abstract description 43
- 238000005260 corrosion Methods 0.000 title claims abstract description 16
- 230000007797 corrosion Effects 0.000 title claims abstract description 16
- 238000003672 processing method Methods 0.000 title claims abstract description 11
- 239000000463 material Substances 0.000 claims abstract description 17
- 229910001220 stainless steel Inorganic materials 0.000 claims abstract description 16
- 239000010935 stainless steel Substances 0.000 claims abstract description 16
- 239000011347 resin Substances 0.000 claims abstract description 15
- 229920005989 resin Polymers 0.000 claims abstract description 15
- 239000003973 paint Substances 0.000 claims abstract description 14
- 238000004381 surface treatment Methods 0.000 claims abstract description 14
- RVNPMZPXRFCIPW-UHFFFAOYSA-N C(C)(=O)OC=C.C(=O)(O)C=CCl Chemical compound C(C)(=O)OC=C.C(=O)(O)C=CCl RVNPMZPXRFCIPW-UHFFFAOYSA-N 0.000 claims abstract description 13
- 238000001035 drying Methods 0.000 claims abstract description 11
- 239000007788 liquid Substances 0.000 claims abstract description 11
- 239000007787 solid Substances 0.000 claims abstract description 9
- 230000004048 modification Effects 0.000 claims abstract description 7
- 238000012986 modification Methods 0.000 claims abstract description 7
- 230000001012 protector Effects 0.000 claims abstract description 7
- 239000011248 coating agent Substances 0.000 claims abstract description 6
- 238000000576 coating method Methods 0.000 claims abstract description 6
- 239000012530 fluid Substances 0.000 claims abstract description 6
- 238000000338 in vitro Methods 0.000 claims abstract description 6
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 32
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical group CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 16
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
- 238000003756 stirring Methods 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 11
- 229920002748 Basalt fiber Polymers 0.000 claims description 8
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims description 8
- 239000011258 core-shell material Substances 0.000 claims description 8
- 239000000839 emulsion Substances 0.000 claims description 8
- 239000005011 phenolic resin Substances 0.000 claims description 8
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims description 8
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 6
- 150000001540 azides Chemical class 0.000 claims description 6
- 238000000498 ball milling Methods 0.000 claims description 6
- 229910052791 calcium Inorganic materials 0.000 claims description 6
- 239000011575 calcium Substances 0.000 claims description 6
- 230000003647 oxidation Effects 0.000 claims description 6
- 238000007254 oxidation reaction Methods 0.000 claims description 6
- 238000005245 sintering Methods 0.000 claims description 6
- 235000019482 Palm oil Nutrition 0.000 claims description 5
- 229910052797 bismuth Inorganic materials 0.000 claims description 5
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims description 5
- ZWLIYXJBOIDXLL-UHFFFAOYSA-N decanedihydrazide Chemical compound NNC(=O)CCCCCCCCC(=O)NN ZWLIYXJBOIDXLL-UHFFFAOYSA-N 0.000 claims description 5
- -1 diisopropyl hydramine Chemical compound 0.000 claims description 5
- 239000011812 mixed powder Substances 0.000 claims description 5
- 239000002540 palm oil Substances 0.000 claims description 5
- 239000002994 raw material Substances 0.000 claims description 5
- YWYZEGXAUVWDED-UHFFFAOYSA-N triammonium citrate Chemical compound [NH4+].[NH4+].[NH4+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O YWYZEGXAUVWDED-UHFFFAOYSA-N 0.000 claims description 5
- 238000006243 chemical reaction Methods 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 3
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 claims description 3
- 239000008367 deionised water Substances 0.000 claims description 3
- 229910021641 deionized water Inorganic materials 0.000 claims description 3
- 239000012467 final product Substances 0.000 claims description 3
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 claims description 3
- BDAGIHXWWSANSR-NJFSPNSNSA-N hydroxyformaldehyde Chemical compound O[14CH]=O BDAGIHXWWSANSR-NJFSPNSNSA-N 0.000 claims description 3
- 239000005543 nano-size silicon particle Substances 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- 229910052814 silicon oxide Inorganic materials 0.000 claims description 3
- 229910000018 strontium carbonate Inorganic materials 0.000 claims description 3
- 238000010792 warming Methods 0.000 claims description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 3
- SJZRECIVHVDYJC-UHFFFAOYSA-N 4-hydroxybutyric acid Chemical compound OCCCC(O)=O SJZRECIVHVDYJC-UHFFFAOYSA-N 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 229910021529 ammonia Inorganic materials 0.000 claims 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims 1
- 239000003292 glue Substances 0.000 claims 1
- 238000000227 grinding Methods 0.000 claims 1
- 239000000843 powder Substances 0.000 claims 1
- 238000012545 processing Methods 0.000 abstract description 7
- 238000005516 engineering process Methods 0.000 abstract description 3
- 239000000853 adhesive Substances 0.000 abstract description 2
- 230000001070 adhesive effect Effects 0.000 abstract description 2
- 230000000694 effects Effects 0.000 abstract description 2
- 230000002708 enhancing effect Effects 0.000 abstract description 2
- 229910052751 metal Inorganic materials 0.000 abstract description 2
- 239000002184 metal Substances 0.000 abstract description 2
- XYGBKMMCQDZQOZ-UHFFFAOYSA-M sodium;4-hydroxybutanoate Chemical compound [Na+].OCCCC([O-])=O XYGBKMMCQDZQOZ-UHFFFAOYSA-M 0.000 description 6
- 239000002390 adhesive tape Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 4
- KLSJWNVTNUYHDU-UHFFFAOYSA-N Amitrole Chemical compound NC1=NC=NN1 KLSJWNVTNUYHDU-UHFFFAOYSA-N 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 2
- 239000000292 calcium oxide Substances 0.000 description 2
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 2
- 239000004816 latex Substances 0.000 description 2
- 229920000126 latex Polymers 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000002161 passivation Methods 0.000 description 2
- 238000005476 soldering Methods 0.000 description 2
- 239000004734 Polyphenylene sulfide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- AOGYCOYQMAVAFD-UHFFFAOYSA-N chlorocarbonic acid Chemical compound OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 description 1
- HGAZMNJKRQFZKS-UHFFFAOYSA-N chloroethene;ethenyl acetate Chemical compound ClC=C.CC(=O)OC=C HGAZMNJKRQFZKS-UHFFFAOYSA-N 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000013569 fruit product Nutrition 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 229920000069 polyphenylene sulfide Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 238000007592 spray painting technique Methods 0.000 description 1
- 239000000052 vinegar Substances 0.000 description 1
- 235000021419 vinegar Nutrition 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/004—Details
- H01G9/08—Housing; Encapsulation
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D127/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers
- C09D127/02—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
- C09D127/04—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C09D127/06—Homopolymers or copolymers of vinyl chloride
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
- C09D4/06—Organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond in combination with a macromolecular compound other than an unsaturated polymer of groups C09D159/00 - C09D187/00
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/08—Anti-corrosive paints
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/61—Additives non-macromolecular inorganic
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/60—Additives non-macromolecular
- C09D7/63—Additives non-macromolecular organic
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/70—Additives characterised by shape, e.g. fibres, flakes or microspheres
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Power Engineering (AREA)
- Inorganic Chemistry (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
- Chemical Treatment Of Metals (AREA)
- Fixed Capacitors And Capacitor Manufacturing Machines (AREA)
Abstract
The invention belongs to capacitor technology fields, and in particular to a kind of processing method for improving capacitor surface corrosion resistance includes herein below:Layer of surface treatment fluid is applied in vitro in capacitor protector, is then sequentially entered three section baking ovens and is dried;Wherein, surface treatment liquid is the modification ternary carboxyl vinyl chloride-vinyl acetate resin that solid content is 15%;Stainless steel capacitor casing surface after the drying is coated with one layer of antirusting paint.Preliminary treatment is carried out to stainless steel capacitor casing surface using surface treatment liquid in the present invention, can make its on stainless steel metal ground hinge, enable what there is antirust function coating effectively to stablize to be attached to capacitor casing surface, stainless steel capacitor casing surface tension after processing reduces, and can improve the adhesive strength of antirust function coating;Antirust function coating material crosslink density rises, and nano effect enhancing, thermal stability, impact flexibility improve, while there is stronger corrosion resistance and resistance to mechanical to scratch performance, and service life extends.
Description
Technical field
The invention belongs to capacitor technology fields, and in particular to a kind of processing side for improving capacitor surface corrosion resistance
Method.
Background technology
As electronic product is to slim, miniaturization, electronic circuit develops to multi-layer board, electronic component also rapidly to
Miniaturization, surface mount manner are fast-developing, therefore sheet component includes sheet type aluminum electrolytic paper roll around as cylinder-like structure
And be bonded as one using adhesive tape, it is packaged after being impregnated with high temperature resistant electrolyte using rubber plug and shell, and such aluminium electroloysis is electric
It is internal since high temperature action can cause the adhesive tape of winding core bag to melt fracture when container is by higher reflow soldering furnace temperature
There is situations such as loose, adhesive tape comes off in core bag, and electrical property is caused to deteriorate, and production reliability reduces, traditional capacitor, band adhesive tape
Mainly it is made using homogenous materials such as polypropylene or polyphenylene sulfides, if fruit product is when by high-temp leadless Reflow Soldering,
It is loose that core bag can occur, production reliability reduces, situations such as adhesive tape comes off, although its theoretical resistance to temperature value is higher, practical application
In be present with softening stretching resistance decline situation in addition be present with the bad phenomenons such as aging cracking, cause product reliability can not
Meet design requirement, with the continuous extension of the application field of electrolytic capacitor, capacitor is widely used in the blocking in electric furnace
Logical, coupling, bypass, filtering, resonant tank, energy conversion, control etc., in order to extend the service life of capacitor, to portion
The surface of point capacitor is handled, due to some existing stainless steel case bulk capacitors, mainly to capacitor casing surface into
Then row shotblasting carries out spray painting protection, which needs using shot-blasting machine, workshop dust, noise pollution compared with
To be serious, industry is also more complicated, has certain restriction to product quality and production efficiency, and its corrosion resistance is not changed effectively
It is kind.
The content of the invention
The purpose of the present invention is being directed to the problem of existing, a kind of processing side for improving capacitor surface corrosion resistance is provided
Method.
The present invention is achieved by the following technical solutions:A kind of processing method for improving capacitor surface corrosion resistance,
Including herein below:
(1)Layer of surface treatment fluid is applied in vitro in capacitor protector, is then sequentially entered three section baking ovens and is dried, three sections
The temperature of baking oven is followed successively by 38 DEG C, 52 DEG C, 80 DEG C;
Wherein, surface treatment liquid is the modification ternary carboxyl vinyl chloride-vinyl acetate resin that solid content is 15%;
(2)Stainless steel capacitor casing surface after the drying is coated with one layer of antirusting paint;
Wherein, antirusting paint includes the raw material of following parts by weight:Water soluble phenol resin 38-42, isopropanol core-shell emulsion
12-16, butyl acrylate 8-12, somsanit 2-4, Nano-lanthanum hydroxide 1-3, p-methyl benzenesulfonic acid 3-6, to toluene sulphur
Acyl azide 2-4 is sintered ash 5-8, palm oil 2-6, sebacic dihydrazide 3-7, bismuth and ammonium citrate 0.2-0.6,3- amino -1,2,4-
Triazole 1.6-1.8, dimethyl sulfoxide (DMSO) 3-6, passive oxidation calcium 2-5, basalt fibre 8-15, mass fraction is 6% citric acid
Aqueous solution 7-10.
As further improvement of these options, it is described three section oven for drying times be followed successively by 0.5-1 it is small when, 1.5-
2 it is small when, 30-40 minutes.
As further improvement of these options, the method for modifying of the modified ternary carboxyl vinyl chloride-vinyl acetate resin is:With 12%
Chromic acid impregnate ternary carboxyl vinyl chloride-vinyl acetate resin 15-20 minutes, then take out and use deionized water rinsing;Ternary carboxylic after treatment again
It is added in base vinyl chloride-vinyl acetate resin and is equivalent to the strontium carbonate of its weight 2%, 1.8% nano silicon oxide and 3% diisopropyl hydramine,
It is dispersed with stirring 10-15 minutes with 3200-3500 revs/min of speed under conditions of 180-200 DEG C, resulting material is diluted with water
Be 15% to solid content, be further continued for scattered stirring 5 minutes to obtain the final product.
As further improvement of these options, the preparation method of the antirusting paint comprises the following steps:
(1)By water soluble phenol resin, isopropanol core-shell emulsion, somsanit, Nano-lanthanum hydroxide, sintering ash,
After 3- amino -1,2,4- triazoles and basalt fibre mix according to the above ratio, in supersonic frequency 22KHz, the item of power 100W
Ultrasonic disperse 25-30 minutes under part, disperse to stir and be warming up to 60-70 DEG C after finishing, when isothermal reaction 2-2.5 is small, be mixed
It is spare to close liquid;
(2)Take butyl acrylate, p-methyl benzenesulfonic acid, p-toluene sulfonyt azide, dimethyl sulfoxide (DMSO) and the mixing of passive oxidation calcium
Afterwards in latex ball mill, with ball material mass ratio 8:1, under conditions of rotating speed is 350 rev/min, when continuous ball milling 1.5 is small, obtain
It is spare to mixed powder;
(3)Surplus stock is added in above-mentioned gained mixed liquor, after stirring evenly, is heated to 160-180 DEG C, isothermal holding
It when 1-2 is small, is then added in together in high speed dispersor with mixed powder, disperses 3-5 points with 1800-2000 revs/min of rotating speed
It is spare to obtain mixed material for clock;
(4)Mixed material is dried to moisture as 22-26% under conditions of 65 DEG C, is then added in again in ball mill, with
Ball material mass ratio 7:1, in rotating speed under conditions of 240 revs/min, when continuous ball milling 2 is small to get.
The present invention has the following advantages compared with prior art:Using surface treatment liquid to stainless steel capacitor protector in the present invention
Body surface face carries out preliminary treatment, can make it on stainless steel metal ground hinge, enabling effective with antirust function coating
Stable is attached to capacitor casing surface, and stainless steel capacitor casing surface tension after processing reduces, and can improve anti-
The adhesive strength of rust functional paint;Antirust function coating material crosslink density rises, nano effect enhancing, thermal stability, punching
Toughness raising is hit, while there is stronger corrosion resistance and resistance to mechanical to scratch performance, service life extends.
Specific embodiment
Embodiment 1
A kind of processing method for improving capacitor surface corrosion resistance, including herein below:
(1)Layer of surface treatment fluid is applied in vitro in capacitor protector, is then sequentially entered three section baking ovens and is dried, three sections
The temperature of baking oven is followed successively by 38 DEG C, 52 DEG C, 80 DEG C;
Wherein, surface treatment liquid is the modification ternary carboxyl vinyl chloride-vinyl acetate resin that solid content is 15%;
(2)Stainless steel capacitor casing surface after the drying is coated with one layer of antirusting paint;
Wherein, antirusting paint includes the raw material of following parts by weight:Water soluble phenol resin 42, isopropanol core-shell emulsion 12,
Butyl acrylate 12, somsanit 2, Nano-lanthanum hydroxide 3, p-methyl benzenesulfonic acid 3, p-toluene sulfonyt azide 3, sintering ash
7, palm oil 6, sebacic dihydrazide 5, bismuth and ammonium citrate 0.2-0.6,3- amino -1,2,4- triazoles 1.8, dimethyl sulfoxide (DMSO) 5,
Passive oxidation calcium 2, basalt fibre 10, mass fraction are 6% aqueous citric acid solution 10.
Wherein, the times of the three sections oven for drying are followed successively by 35 minutes, 1.5 it is small when, 30 minutes.
Wherein, the method for modifying of the modified ternary carboxyl vinyl chloride-vinyl acetate resin is:Ternary carboxyl chlorine vinegar is impregnated with 12% chromic acid
Resin 15-20 minutes, then takes out and uses deionized water rinsing;It adds in and is equivalent in ternary carboxyl vinyl chloride-vinyl acetate resin after treatment again
The strontium carbonate of its weight 2%, 1.8% nano silicon oxide and 3% diisopropyl hydramine, under conditions of 180 DEG C with 3500 turns/
The speed of minute is dispersed with stirring 10 minutes, and it is 15% that resulting material is diluted with water to solid content, is further continued for scattered stirring 5 minutes
To obtain the final product.
Wherein, the preparation method of the antirusting paint comprises the following steps:
(1)By water soluble phenol resin, isopropanol core-shell emulsion, somsanit, Nano-lanthanum hydroxide, sintering ash,
After 3- amino -1,2,4- triazoles and basalt fibre mix according to the above ratio, in supersonic frequency 22KHz, the item of power 100W
Ultrasonic disperse 30 minutes under part disperse to stir and be warming up to 65 DEG C after finishing, when isothermal reaction 2 is small, it is spare to obtain mixed liquor;
(2)Take butyl acrylate, p-methyl benzenesulfonic acid, p-toluene sulfonyt azide, dimethyl sulfoxide (DMSO) and the mixing of passive oxidation calcium
Afterwards in latex ball mill, with ball material mass ratio 8:1, under conditions of rotating speed is 350 rev/min, when continuous ball milling 1.5 is small, obtain
It is spare to mixed powder;
(3)Surplus stock is added in above-mentioned gained mixed liquor, after stirring evenly, is heated to 160-180 DEG C, isothermal holding
It when 1-2 is small, is then added in together in high speed dispersor with mixed powder, disperses 3-5 points with 1800-2000 revs/min of rotating speed
It is spare to obtain mixed material for clock;
(4)It is 24% that mixed material is dried to moisture under conditions of 65 DEG C, is then added in again in ball mill, with ball
Expect mass ratio 7:1, in rotating speed under conditions of 240 revs/min, when continuous ball milling 2 is small to get.
Stainless steel capacitor case carries out salt spray test, experimental result after method processing in the present embodiment, to its housing
, without significant change, in addition to set experiment burin-in process 30 days under conditions of 200 DEG C, tensile strength is place in 1800h
86.7% before reason, performance is stablized, and service life extends.
Embodiment 2
A kind of processing method for improving capacitor surface corrosion resistance, including herein below:
(1)Layer of surface treatment fluid is applied in vitro in capacitor protector, is then sequentially entered three section baking ovens and is dried, three sections
The temperature of baking oven is followed successively by 38 DEG C, 52 DEG C, 80 DEG C;
Wherein, surface treatment liquid is the modification ternary carboxyl vinyl chloride-vinyl acetate resin that solid content is 15%;
(2)Stainless steel capacitor casing surface after the drying is coated with one layer of antirusting paint;
Wherein, antirusting paint includes the raw material of following parts by weight:Water soluble phenol resin 40, isopropanol core-shell emulsion 14,
Butyl acrylate 8, somsanit 3, Nano-lanthanum hydroxide 2, p-methyl benzenesulfonic acid 4, p-toluene sulfonyt azide 2, sintering ash 5,
Palm oil 6, sebacic dihydrazide 7, bismuth and ammonium citrate 0.6,3- amino -1,2,4- triazoles 1.7, dimethyl sulfoxide (DMSO) 3-6, passivation
Calcium oxide 4, basalt fibre 12, mass fraction are 6% aqueous citric acid solution 8.
Wherein, the times of the three sections oven for drying are followed successively by 45 minutes, 2 it is small when, 40 minutes.
The other content of embodiment 2 is same as Example 1.
Stainless steel capacitor case carries out salt spray test, experimental result after method processing in the present embodiment, to its housing
, without significant change, in addition to set experiment burin-in process 30 days under conditions of 200 DEG C, tensile strength is place in 1800h
87.2% before reason, performance is stablized, and service life extends.
Embodiment 3
A kind of processing method for improving capacitor surface corrosion resistance, including herein below:
(1)Layer of surface treatment fluid is applied in vitro in capacitor protector, is then sequentially entered three section baking ovens and is dried, three sections
The temperature of baking oven is followed successively by 38 DEG C, 52 DEG C, 80 DEG C;
Wherein, surface treatment liquid is the modification ternary carboxyl vinyl chloride-vinyl acetate resin that solid content is 15%;
(2)Stainless steel capacitor casing surface after the drying is coated with one layer of antirusting paint;
Wherein, antirusting paint includes the raw material of following parts by weight:Water soluble phenol resin 38, isopropanol core-shell emulsion 16,
Butyl acrylate 10, somsanit 2, Nano-lanthanum hydroxide 2, p-methyl benzenesulfonic acid 4, p-toluene sulfonyt azide 3, sintering ash
7, palm oil 5, sebacic dihydrazide 4, bismuth and ammonium citrate 0.6,3- amino -1,2,4- triazoles 1.6, dimethyl sulfoxide (DMSO) 3, passivation
Calcium oxide 5, basalt fibre 8-15, mass fraction are 6% aqueous citric acid solution 10.
Wherein, the times of the three sections oven for drying are followed successively by 55 minutes, 2 it is small when, 30 minutes.
The other content of embodiment 3 is same as Example 1.
Stainless steel capacitor case carries out salt spray test, experimental result after method processing in the present embodiment, to its housing
, without significant change, in addition to set experiment burin-in process 30 days under conditions of 200 DEG C, tensile strength is place in 1800h
87.4% before reason, performance is stablized, and service life extends.
Claims (4)
1. a kind of processing method for improving capacitor surface corrosion resistance, which is characterized in that including herein below:
Layer of surface treatment fluid is applied in vitro in capacitor protector, is then sequentially entered three section baking ovens and is dried, three section baking ovens
Temperature is followed successively by 38 DEG C, 52 DEG C, 80 DEG C;
Wherein, surface treatment liquid is the modification ternary carboxyl vinyl chloride-vinyl acetate resin that solid content is 15%;
Stainless steel capacitor casing surface after the drying is coated with one layer of antirusting paint;
Wherein, antirusting paint includes the raw material of following parts by weight:Water soluble phenol resin 38-42, isopropanol core-shell emulsion 12-
16, butyl acrylate 8-12, somsanit 2-4, Nano-lanthanum hydroxide 1-3, p-methyl benzenesulfonic acid 3-6, tolysulfonyl are folded
Nitrogen 2-4 is sintered ash 5-8, palm oil 2-6, sebacic dihydrazide 3-7, bismuth and ammonium citrate 0.2-0.6,3- amino -1,2, tri- nitrogen of 4-
Azoles 1.6-1.8, dimethyl sulfoxide (DMSO) 3-6, passive oxidation calcium 2-5, basalt fibre 8-15, the citric acid that mass fraction is 6% are water-soluble
Liquid 7-10.
A kind of 2. processing method for improving capacitor surface corrosion resistance as described in claim 1, which is characterized in that three section
The time of oven for drying be followed successively by 0.5-1 it is small when, when 1.5-2 is small, 30-40 minutes.
A kind of 3. processing method for improving capacitor surface corrosion resistance as described in claim 1, which is characterized in that the modification
The method of modifying of ternary carboxyl vinyl chloride-vinyl acetate resin is:Ternary carboxyl vinyl chloride-vinyl acetate resin is impregnated with 12% chromic acid 15-20 minutes, Ran Houqu
Go out to use deionized water rinsing;Again in ternary carboxyl vinyl chloride-vinyl acetate resin after treatment add in be equivalent to its weight 2% strontium carbonate,
1.8% nano silicon oxide and 3% diisopropyl hydramine, with 3200-3500 revs/min of speed under conditions of 180-200 DEG C
Degree is dispersed with stirring 10-15 minutes, and it is 15% that resulting material is diluted with water to solid content, is further continued for scattered stirring 5 minutes to obtain the final product.
A kind of 4. processing method for improving capacitor surface corrosion resistance as described in claim 1, which is characterized in that the antirust
The preparation method of coating comprises the following steps:
(1)By water soluble phenol resin, isopropanol core-shell emulsion, somsanit, Nano-lanthanum hydroxide, sintering ash, 3- ammonia
After base -1,2,4- triazoles and basalt fibre are by the mixing of above-mentioned weight/power ratio part, in supersonic frequency 22KHz, the item of power 100W
Ultrasonic disperse 25-30 minutes under part, disperse to stir and be warming up to 60-70 DEG C after finishing, when isothermal reaction 2-2.5 is small, be mixed
It is spare to close liquid;
(2)Take butyl acrylate, p-methyl benzenesulfonic acid, p-toluene sulfonyt azide, dimethyl sulfoxide (DMSO) and passive oxidation calcium mixing after glue
In milk-globule grinding machine, with ball material mass ratio 8:1, under conditions of rotating speed is 350 rev/min, when continuous ball milling 1.5 is small, mixed
It is spare to close powder;
(3)Surplus stock is added in above-mentioned gained mixed liquor, after stirring evenly, is heated to 160-180 DEG C, isothermal holding 1-2
Hour, it then adds in high speed dispersor with mixed powder, is disperseed 3-5 minutes with 1800-2000 revs/min of rotating speed together,
It is spare to obtain mixed material;
(4)Mixed material is dried to moisture as 22-26% under conditions of 65 DEG C, is then added in again in ball mill, with ball material
Mass ratio 7:1, in rotating speed under conditions of 240 revs/min, when continuous ball milling 2 is small to get.
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JPH04127413A (en) * | 1990-05-28 | 1992-04-28 | Kobe Steel Ltd | Laminated aluminum material for electrolytic-capacitor case use |
JPH0786099A (en) * | 1993-09-10 | 1995-03-31 | Matsushita Electric Ind Co Ltd | Electrolytic capacitor |
CN102311687B (en) * | 2011-09-28 | 2014-01-01 | 天长市巨龙车船涂料有限公司 | Modified vinyl chloride-acetate copolymer heavy duty anticorrosion paint |
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