CN108822677A - A kind of preparation method of motor anticorrosion finishing coat - Google Patents
A kind of preparation method of motor anticorrosion finishing coat Download PDFInfo
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- CN108822677A CN108822677A CN201810247198.1A CN201810247198A CN108822677A CN 108822677 A CN108822677 A CN 108822677A CN 201810247198 A CN201810247198 A CN 201810247198A CN 108822677 A CN108822677 A CN 108822677A
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- 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
- C09D163/00—Coating compositions based on epoxy resins; Coating compositions based on derivatives of epoxy resins
-
- 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
- C09D7/65—Additives macromolecular
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2227—Oxides; Hydroxides of metals of aluminium
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2201/00—Properties
- C08L2201/08—Stabilised against heat, light or radiation or oxydation
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Abstract
The present invention provides a kind of motor preparation methods of anticorrosion finishing coat, include the following steps：（1）Phosphoric acid and deionized water are subjected to mixed dissolution and obtain phosphoric acid solution, the weight ratio of phosphoric acid and deionized water is 1:1-1.1；（2）Phosphoric acid solution is heated to 86-92 DEG C, and is stirred；（3）It is slowly added to aluminium hydroxide, speed is 6-10 parts/h, while being warming up to 110-120 DEG C, keeps this temperature stirring 1.5-2h transparent to solution；（4）It is cooling, and adjusting solution ph is 1.47-1.48；（5）Deionized water is added, silica solution, refractory aggregate, dispersing agent, chelating agent, aqueous epoxy resins, polyvinylpyrrolidone and neopelex are added while stirring；（6）It is transferred in Ultrasound Instrument ultrasound 30-50min to obtain the final product.Finishing coat prepared by this method has good anticorrosion ability, and salt fog resistance is good, while also having extraordinary adhesion.
Description
Technical field
The present invention relates to a kind of motor preparation methods of anticorrosion finishing coat.
Background technique
With the development of economy and society, the development of materials industry is even more to make rapid progress, the environment that a variety of materials use is also more next
It is more harsh, how anti-corrosive properties are improved, extending it using the time is to improve value, an energy saving extraordinary mode.And
It the use of antisepsis finishing paint is exactly one of one of effective ways for improving anti-corrosive properties.Anticorrosion finishing coat refers to that being coated on body surface exists
Film can be formed under conditions of certain and plays protection, decoration or other specific functions（Insulation, antirust, mould proof, heat-resisting etc.）One
Class I liquid I.The anti-corrosive properties of finishing coat how are improved, while not influencing its adhesion property, are to need constantly research and improved project.
Summary of the invention
Technical problems to be solved：The object of the present invention is to provide a kind of motor preparation method of anticorrosion finishing coat, institutes
The finishing coat of preparation has good anticorrosion ability, and salt fog resistance is good, still without rust spot after 200h, while also having extraordinary
Adhesion.
Technical solution：A kind of preparation method of motor anticorrosion finishing coat, ingredient by weight, include the following steps：
（1）30-50 parts of phosphoric acid and deionized water are subjected to mixed dissolution and obtain phosphoric acid solution, the weight ratio of phosphoric acid and deionized water is
1:1-1.1；
（2）Phosphoric acid solution is heated to 86-92 DEG C, and is stirred；
（3）It is slowly added to aluminium hydroxide, speed is 6-10 parts/h, while being warming up to 110-120 DEG C, this temperature is kept to stir 1.5-
2h is transparent to solution；
（4）It is cooling, and adjusting solution ph is 1.47-1.48；
（5）Be added 50-80 part deionized waters, while stirring addition 5-10 parts of silica solution, 1-2 parts of refractory aggregates, 2-5 parts of dispersing agents,
2-4 parts of chelating agents, 10-20 parts of aqueous epoxy resins, 2-5 parts of polyvinylpyrrolidones and 1-2 parts of neopelexes；
（6）It is transferred in Ultrasound Instrument ultrasound 30-50min to obtain the final product.
It is further preferred that the dispersing agent includes polyethylene glycol 200, sodium metnylene bis-naphthalene sulfonate, enuatrol.
It is further preferred that the chelating agent is one or more of tartaric acid, citric acid, gluconic acid or phytic acid.
It is further preferred that the refractory aggregate is magnesite clinker, burnt dolomite, alabaster, spinelle, zircon or height
One or more of furnace slag.
A kind of preparation method of motor anticorrosion finishing coat according to claim 1, it is characterised in that：It is described resistance to
The partial size of fiery aggregate is 1-2mm.
Beneficial effect：
1. silica solution makes surface extra hydroxyl occur by the hydroxyl in absorption water, thus increase space net structure, hydroxyl
The introducing of base not only changes the reticular structure of colloid, while will limit the value of colloidal solution, the hydroxyl dissociation of introducing, ties net
The electrification of structure surface, thus change the value of solution, in film forming assimilation process, trifoliate orange, energy due to silica sol particle huge ratio table
Enough uniform package electrode material surfaces, so that homogeneous film formation, guarantees the bond strength of film.So the reticular structure of silica solution
The rheological characteristic that can be good at controlling finishing coat, makes coating smooth even.
2. silica solution forms hydrogen bond with the extra group in finishing coat and links together, increases reticular structure, increase finishing coat
Cohesive force improves the adhesion strength and stability of finishing coat with this.Meanwhile the colloidal osmotic power of silica solution is strong, can pass through capillary
Effect is penetrated into inside motor material, and the mutual cohesive force between finishing coat and motor material is further enhanced.
3. aqueous epoxy resins crosslink at high temperature with silica solution, organic siliconresin is formed, which contains base
Group makes film have high-fire resistance, hydrophobicity, while can effectively enhance toughness and waterproofness of finishing coat etc..
4. finishing coat of the present invention has good anticorrosion ability, salt fog resistance is good, still without rust spot after 200h, simultaneously also
With extraordinary adhesion.
Specific embodiment
Embodiment 1
A kind of preparation method of motor anticorrosion finishing coat, ingredient by weight, include the following steps：
（1）30 parts of phosphoric acid and deionized water are subjected to mixed dissolution and obtain phosphoric acid solution, the weight ratio of phosphoric acid and deionized water is 1:1；
（2）Phosphoric acid solution is heated to 86 DEG C, and is stirred；
（3）It is slowly added to aluminium hydroxide, speed is 6 parts/h, while being warming up to 110 DEG C, this temperature is kept to stir 1.5h to solution
It is transparent；
（4）It is cooling, and adjusting solution ph is 1.47；
（5）50 parts of deionized waters are added, 5 parts of silica solution, 1 part of magnesite clinker, 2 parts of polyethylene glycol 200s, 2 parts are added while stirring
Citric acid, 10 parts of aqueous epoxy resins, 2 parts of polyvinylpyrrolidones and 1 part of neopelex；
（6）It is transferred in Ultrasound Instrument ultrasound 30min to obtain the final product.
Embodiment 2
A kind of preparation method of motor anticorrosion finishing coat, ingredient by weight, include the following steps：
（1）35 parts of phosphoric acid and deionized water are subjected to mixed dissolution and obtain phosphoric acid solution, the weight ratio of phosphoric acid and deionized water is 1:1；
（2）Phosphoric acid solution is heated to 88 DEG C, and is stirred；
（3）It is slowly added to aluminium hydroxide, speed is 7 parts/h, while being warming up to 115 DEG C, this temperature is kept to stir 1.5h to solution
It is transparent；
（4）It is cooling, and adjusting solution ph is 1.47；
（5）60 parts of deionized waters are added, 6 parts of silica solution, 1.5 parts of burnt dolomites, 3 parts of methylene dinaphthalene sulphurs are added while stirring
Sour sodium, 3 parts of gluconic acids, 15 parts of aqueous epoxy resins, 3 parts of polyvinylpyrrolidones and 1.5 parts of neopelexes；
（6）It is transferred in Ultrasound Instrument ultrasound 35min to obtain the final product.
Embodiment 3
A kind of preparation method of motor anticorrosion finishing coat, ingredient by weight, include the following steps：
（1）40 parts of phosphoric acid and deionized water are subjected to mixed dissolution and obtain phosphoric acid solution, the weight ratio of phosphoric acid and deionized water is 1:1.1；
（2）Phosphoric acid solution is heated to 90 DEG C, and is stirred；
（3）It is slowly added to aluminium hydroxide, speed is 8 parts/h, while being warming up to 115 DEG C, keeps this temperature stirring 2h transparent to solution；
（4）It is cooling, and adjusting solution ph is 1.48；
（5）70 parts of deionized waters are added, while stirring be added 9 parts of silica solution, 1.5 parts of alabasters, 4 parts of enuatrols, 3 parts of tartaric acid,
15 parts of aqueous epoxy resins, 4 parts of polyvinylpyrrolidones and 1.5 parts of neopelexes；
（6）It is transferred in Ultrasound Instrument ultrasound 40min to obtain the final product.
Embodiment 4
A kind of preparation method of motor anticorrosion finishing coat, ingredient by weight, include the following steps：
（1）50 parts of phosphoric acid and deionized water are subjected to mixed dissolution and obtain phosphoric acid solution, the weight ratio of phosphoric acid and deionized water is 1:1.1；
（2）Phosphoric acid solution is heated to 92 DEG C, and is stirred；
（3）It is slowly added to aluminium hydroxide, speed is 10 parts/h, while being warming up to 120 DEG C, keeps this temperature stirring 2h transparent to solution；
（4）It is cooling, and adjusting solution ph is 1.48；
（5）80 parts of deionized waters are added, 10 parts of silica solution, 2 parts of blast-furnace cinders, 5 parts of polyethylene glycol 200s, 4 parts are added while stirring
Phytic acid, 20 parts of aqueous epoxy resins, 5 parts of polyvinylpyrrolidones and 2 parts of neopelexes；
（6）It is transferred in Ultrasound Instrument ultrasound 50min to obtain the final product.
Comparative example 1
The present embodiment is with embodiment 1 the difference is that not containing silica solution, specially：
A kind of preparation method of motor anticorrosion finishing coat, ingredient by weight, include the following steps：
（1）30 parts of phosphoric acid and deionized water are subjected to mixed dissolution and obtain phosphoric acid solution, the weight ratio of phosphoric acid and deionized water is 1:1；
（2）Phosphoric acid solution is heated to 86 DEG C, and is stirred；
（3）It is slowly added to aluminium hydroxide, speed is 6 parts/h, while being warming up to 110 DEG C, this temperature is kept to stir 1.5h to solution
It is transparent；
（4）It is cooling, and adjusting solution ph is 1.47；
（5）50 parts of deionized waters are added, 1 part of magnesite clinker, 2 parts of polyethylene glycol 200s, 2 parts of citric acids, 10 parts are added while stirring
Aqueous epoxy resins, 2 parts of polyvinylpyrrolidones and 1 part of neopelex；
（6）It is transferred in Ultrasound Instrument ultrasound 30min to obtain the final product.
Comparative example 2
The present embodiment is with embodiment 1 the difference is that not containing polyethylene glycol 200, specially：
A kind of preparation method of motor anticorrosion finishing coat, ingredient by weight, include the following steps：
（1）30 parts of phosphoric acid and deionized water are subjected to mixed dissolution and obtain phosphoric acid solution, the weight ratio of phosphoric acid and deionized water is 1:1；
（2）Phosphoric acid solution is heated to 86 DEG C, and is stirred；
（3）It is slowly added to aluminium hydroxide, speed is 6 parts/h, while being warming up to 110 DEG C, this temperature is kept to stir 1.5h to solution
It is transparent；
（4）It is cooling, and adjusting solution ph is 1.47；
（5）50 parts of deionized waters are added, while stirring be added 5 parts of silica solution, 1 part of magnesite clinker, 2 parts of citric acids, 10 parts it is aqueous
Epoxy resin, 2 parts of polyvinylpyrrolidones and 1 part of neopelex；
（6）It is transferred in Ultrasound Instrument ultrasound 30min to obtain the final product.
Comparative example 3
The present embodiment is with embodiment 1 the difference is that replacing polyvinylpyrrolidone with aqueous epoxy resins, specially：
A kind of preparation method of motor anticorrosion finishing coat, ingredient by weight, include the following steps：
（1）30 parts of phosphoric acid and deionized water are subjected to mixed dissolution and obtain phosphoric acid solution, the weight ratio of phosphoric acid and deionized water is 1:1；
（2）Phosphoric acid solution is heated to 86 DEG C, and is stirred；
（3）It is slowly added to aluminium hydroxide, speed is 6 parts/h, while being warming up to 110 DEG C, this temperature is kept to stir 1.5h to solution
It is transparent；
（4）It is cooling, and adjusting solution ph is 1.47；
（5）50 parts of deionized waters are added, 5 parts of silica solution, 1 part of magnesite clinker, 2 parts of polyethylene glycol 200s, 2 parts are added while stirring
Citric acid, 12 parts of aqueous epoxy resins and 1 part of neopelex；
（6）It is transferred in Ultrasound Instrument ultrasound 30min to obtain the final product.
By motor metal material surface after soda acid is washed ultrasonic wave water washing, wipe dry surface with filter paper, picked and prepared with masking liquid stick
Finishing coat of the present invention be uniformly coated to its surface and dried at 250 DEG C.
Salt-fog resistant test：Motor material after drying is placed in the closed crisper equipped with sodium chloride solution, every compartment
Time observes situations such as steel disc surface oxidisation and blistering.
The adhesion of finishing coat is measured according to national standard GB/T2522-1988.
The salt spray resistance of table 1 motor anticorrosion finishing coat
The adhesion of table 2 motor anticorrosion finishing coat
The partial properties index of the anticorrosion finishing coat of motor prepared by the method for the present invention is seen the above table, it may be seen that of the invention
Finishing coat has good anticorrosion ability, and salt fog resistance is good, still without rust spot after 200h, while this finishing coat as can be seen from Table 2
Also there is extraordinary adhesion.
Claims (5)
1. a kind of motor preparation method of anticorrosion finishing coat, it is characterised in that：Ingredient by weight, includes the following steps：
（1）30-50 parts of phosphoric acid and deionized water are subjected to mixed dissolution and obtain phosphoric acid solution, the weight ratio of phosphoric acid and deionized water is
1:1-1.1；
（2）Phosphoric acid solution is heated to 86-92 DEG C, and is stirred；
（3）It is slowly added to aluminium hydroxide, speed is 6-10 parts/h, while being warming up to 110-120 DEG C, this temperature is kept to stir 1.5-
2h is transparent to solution；
（4）It is cooling, and adjusting solution ph is 1.47-1.48；
（5）50-80 parts of deionized waters are added, 5-10 parts of silica solution, 1-2 parts of refractory aggregates, 2-5 parts of dispersions are added while stirring
Agent, 2-4 parts of chelating agents, 10-20 parts of aqueous epoxy resins, 2-5 parts of polyvinylpyrrolidones and 1-2 parts of dodecyl benzene sulfonic acid
Sodium；
（6）It is transferred in Ultrasound Instrument ultrasound 30-50min to obtain the final product.
2. a kind of preparation method of motor anticorrosion finishing coat according to claim 1, it is characterised in that：The dispersion
Agent includes polyethylene glycol 200, sodium metnylene bis-naphthalene sulfonate, enuatrol.
3. a kind of preparation method of motor anticorrosion finishing coat according to claim 1, it is characterised in that：The chelating
Agent is one or more of tartaric acid, citric acid, gluconic acid or phytic acid.
4. a kind of preparation method of motor anticorrosion finishing coat according to claim 1, it is characterised in that：The fire resisting
Aggregate is one or more of magnesite clinker, burnt dolomite, alabaster, spinelle, zircon or blast-furnace cinder.
5. a kind of preparation method of motor anticorrosion finishing coat according to claim 1, it is characterised in that：The fire resisting
The partial size of aggregate is 1-2mm.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201810247198.1A CN108822677A (en) | 2018-03-23 | 2018-03-23 | A kind of preparation method of motor anticorrosion finishing coat |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
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| CN201810247198.1A CN108822677A (en) | 2018-03-23 | 2018-03-23 | A kind of preparation method of motor anticorrosion finishing coat |
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| CN108822677A true CN108822677A (en) | 2018-11-16 |
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| CN201810247198.1A Withdrawn CN108822677A (en) | 2018-03-23 | 2018-03-23 | A kind of preparation method of motor anticorrosion finishing coat |
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN112516378A (en) * | 2020-12-02 | 2021-03-19 | 浙江工业大学 | Preparation method of phytic acid/silk fibroin/calcined dolomite bone adhesive |
| CN114591670A (en) * | 2022-03-03 | 2022-06-07 | 国网山东省电力公司电力科学研究院 | Anti-condensation coating for high-voltage switch cabinet and preparation method and application thereof |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102746766A (en) * | 2012-07-23 | 2012-10-24 | 江苏华夏制漆科技有限公司 | Water -borne anticorrosion paint and method for preparing same |
| US20130337266A1 (en) * | 2011-02-18 | 2013-12-19 | Wacker Chemie Ag | Modified composite particles |
-
2018
- 2018-03-23 CN CN201810247198.1A patent/CN108822677A/en not_active Withdrawn
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20130337266A1 (en) * | 2011-02-18 | 2013-12-19 | Wacker Chemie Ag | Modified composite particles |
| CN102746766A (en) * | 2012-07-23 | 2012-10-24 | 江苏华夏制漆科技有限公司 | Water -borne anticorrosion paint and method for preparing same |
Non-Patent Citations (1)
| Title |
|---|
| 郭海珠: "《实用耐火原料手册》", 31 January 2009, 中国建材工业出版社 * |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN112516378A (en) * | 2020-12-02 | 2021-03-19 | 浙江工业大学 | Preparation method of phytic acid/silk fibroin/calcined dolomite bone adhesive |
| CN114591670A (en) * | 2022-03-03 | 2022-06-07 | 国网山东省电力公司电力科学研究院 | Anti-condensation coating for high-voltage switch cabinet and preparation method and application thereof |
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