CN102942846A - Coating scheme of anti-corrosion paint - Google Patents
Coating scheme of anti-corrosion paint Download PDFInfo
- Publication number
- CN102942846A CN102942846A CN2012105378099A CN201210537809A CN102942846A CN 102942846 A CN102942846 A CN 102942846A CN 2012105378099 A CN2012105378099 A CN 2012105378099A CN 201210537809 A CN201210537809 A CN 201210537809A CN 102942846 A CN102942846 A CN 102942846A
- Authority
- CN
- China
- Prior art keywords
- protective system
- coating method
- coating
- described protective
- substrate surface
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 238000000576 coating method Methods 0.000 title claims abstract description 35
- 239000011248 coating agent Substances 0.000 title claims abstract description 21
- 238000005260 corrosion Methods 0.000 title abstract description 9
- 239000003973 paint Substances 0.000 title abstract 2
- 239000000463 material Substances 0.000 claims abstract description 8
- 230000008021 deposition Effects 0.000 claims abstract description 7
- 229920000049 Carbon (fiber) Polymers 0.000 claims abstract description 6
- 239000004642 Polyimide Substances 0.000 claims abstract description 6
- 239000004917 carbon fiber Substances 0.000 claims abstract description 6
- 239000008367 deionised water Substances 0.000 claims abstract description 6
- 229910021641 deionized water Inorganic materials 0.000 claims abstract description 6
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229920001721 polyimide Polymers 0.000 claims abstract description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 6
- 238000005507 spraying Methods 0.000 claims abstract description 4
- 230000001680 brushing effect Effects 0.000 claims abstract description 3
- 238000000034 method Methods 0.000 claims description 23
- 230000001681 protective effect Effects 0.000 claims description 16
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 15
- 239000000758 substrate Substances 0.000 claims description 15
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 10
- 239000002245 particle Substances 0.000 claims description 9
- 230000035800 maturation Effects 0.000 claims description 8
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 7
- 238000012545 processing Methods 0.000 claims description 6
- 239000007921 spray Substances 0.000 claims description 6
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 claims description 5
- 229910052684 Cerium Inorganic materials 0.000 claims description 5
- 229910000838 Al alloy Inorganic materials 0.000 claims description 3
- 229910000831 Steel Inorganic materials 0.000 claims description 3
- 239000004411 aluminium Substances 0.000 claims description 3
- 229910052782 aluminium Inorganic materials 0.000 claims description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- 239000010959 steel Substances 0.000 claims description 3
- MZSAMHOCTRNOIZ-UHFFFAOYSA-N 3-[4-(aminomethyl)-6-(trifluoromethyl)pyridin-2-yl]oxy-N-phenylaniline Chemical compound NCC1=CC(=NC(=C1)C(F)(F)F)OC=1C=C(NC2=CC=CC=C2)C=CC=1 MZSAMHOCTRNOIZ-UHFFFAOYSA-N 0.000 claims description 2
- 238000005137 deposition process Methods 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 claims 1
- 229910052761 rare earth metal Inorganic materials 0.000 abstract description 5
- 239000000203 mixture Substances 0.000 abstract description 4
- 239000002904 solvent Substances 0.000 abstract description 3
- -1 rare earth compound Chemical class 0.000 abstract description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 abstract 1
- 238000001914 filtration Methods 0.000 abstract 1
- 230000007797 corrosion Effects 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- ZMIGMASIKSOYAM-UHFFFAOYSA-N cerium Chemical compound [Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce] ZMIGMASIKSOYAM-UHFFFAOYSA-N 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000007739 conversion coating Methods 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 239000007800 oxidant agent Substances 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 150000002910 rare earth metals Chemical class 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- 230000000711 cancerogenic effect Effects 0.000 description 1
- 231100000315 carcinogenic Toxicity 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 229940126214 compound 3 Drugs 0.000 description 1
- 229940125898 compound 5 Drugs 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 230000036314 physical performance Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 230000007096 poisonous effect Effects 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 238000002203 pretreatment Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000001932 seasonal effect Effects 0.000 description 1
- 231100000167 toxic agent Toxicity 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Abstract
The invention discloses a coating scheme of anti-corrosion paint, which comprises the steps of: mixing the components such as siloxane, solvent, silica particles, rare earth compound, deionized water, catalyst, carbon fiber and polyimide, and then curing; filtering the cured mixture; and spraying, brushing or impregnating the filtered mixture on the surface of base material, wherein a coating is formed on the surface of the base material after deposition, thus realizing surface anti-corrosion treatment.
Description
Technical field
The present invention relates to a kind of protective system coating method, relate in particular to a kind of metal structure surface that is applicable to, have the coating method of the environmental protection coating material of excellent gloss and mechanical and physical performance and aromatic free solvent.
Background technology
In modern industry and daily life, corrosion of metal is seen everywhere, and the destruction of the forms such as crevice corrosion, stress corrosion and corrosion fatigue that especially occur in the storage vessel of a fuel oil dangerization product is caused great potential safety hazard for people's lives.
The metal protection method that adopts at present can roughly be divided three classes: a class is to carry out anodic oxidation treatment, namely form the anode oxide film of one deck tens micron thickness in the metallic surface, but because the anode oxidation process power consumption is large, and electrolyte solution is seriously polluted, be difficult to process, use its application to be restricted; Equations of The Second Kind is chemical conversion film, being about to metal parts is immersed in the solution of definite composition, rely at a certain temperature chemical reaction to form one deck chemical conversion film, now most widely used is the oxidation of chromic salt chemistry, but chromic salt is a kind of carcinogenic toxicant, and the world environments protective tissue has proposed restriction and used chromic salt and other to contain chromate compound; The 3rd class is organic coating, namely applies one deck organic coating in the metallic surface, with outward appearance and the physical and chemical performance that improves metal.People begin rare earth element is used in the aseptic technic of metallic surface in recent years.
The rare-earth conversion coatings film technique develops into today, and people have carried out a large amount of improvement to various film-forming process, and the performance of film also is improved.At present the rare-earth conversion coatings technology mainly is immersion treatment, and this technological operation is simple, be easy to safeguard; But its drawback is that the long period of soaking process treatment time is oversize, and formed rete is thinner and relatively poor with the sticking power of base material.Find through long-term exploratory development, add strong oxidizer in the soaking solution, such as H
2O
2, KMnO
4, (NH
4)
2S
2O
8Etc. strong oxide compound, rate of film build is improved greatly, the treatment time shortens dramatically, and the treatment soln temperature is not high yet simultaneously, can at room temperature use.But because the existence of strong oxidizer is so that the less stable for the treatment of process.
The problem that exists in order to solve the rare-earth conversion coatings treatment process, the present invention proposes a kind of improved protective system coating method.This method anticorrosion with low cost, remarkable in economical benefits can be carried out normal temperature and be spread, and coating processes is simple, and solution is environment friendly and pollution-free.
Summary of the invention
The objective of the invention is for the deficiencies in the prior art part, provide a kind of coating method of environment friendly corrosion protection coating, in order to solve the protection against corrosion difficult problem of the surfaces externally and internally applications such as steel, aluminium, especially aluminium alloy, and coating aromatic free solvent, do not contain strong oxidizer, without poisonous pigment, be fit to various constructional methods, application is not subject to seasonal restrictions, and construction technology is simple and convenient, and technical costs is cheap, good environmental protection.
The present invention is achieved by the following technical solutions:
(1) prepare following component (mass parts):
A APTES 1-10;
B propyl alcohol 40-60;
C SiO
2Particle 1-5;
The oxide compound 1-5 of d cerium;
E deionized water 5-25;
F acetic acid 1-3;
G carbon fiber 5-7;
H polyimide 1-3;
(2) with carrying out maturation process after the above component mixing, then spray, brush or be immersed in substrate surface, form coating at substrate surface after the deposition, realize the surface anticorrosion processing.
Embodiment
The present invention relates to a kind of coating scheme of protective system, after the various components of protective system are mixed, carry out maturation process, again the mixture after the slaking is filtered, then spray, brush or be immersed in substrate surface, form coating at substrate surface after the deposition, realize the surface anticorrosion processing.
Described SiO
2The particle diameter of particle is the 50-100 nanometer.
Described maturation process is to leave standstill at normal temperatures 50-60 hour.
Described base material is steel or aluminium, preferred aluminium alloy.
Heat in the deposition process after spraying, brushing or dipping, Heating temperature is to heat 1 minute to 1 hour under 50 ℃ to the 150 ℃ temperature.
The thickness of described coating is 1 micron to 10 microns, preferred 1 micron to 5 microns.The preferred method that adopts spraying or brush forms coating at substrate surface.
Protective system coating method disclosed by the invention is simple, convenient, quick, reliable, and raw material is cheap, this method can be simply in conjunction with enter the existing pre-treatment that comprises coating and after in the conventional production line of other postprocessing working procedures of substrate material, substantially need not to carry out other adjustment on the equipment, is the Eco-power production technique of a kind of height.
The below elaborates with embodiment to the present invention, but protection scope of the present invention is not limited to following embodiment.
Embodiment 1
(1) prepare following component (mass parts):
A APTES 1;
B propyl alcohol 40;
C SiO
2Particle 1;
The oxide compound 1 of d cerium;
E deionized water 5;
F acetic acid 1;
G carbon fiber 5;
H polyimide 1;
(2) with carrying out maturation process after the above component mixing, then spray, brush or be immersed in substrate surface, form coating at substrate surface after the deposition, realize the surface anticorrosion processing.
Embodiment 2
(1) prepare following component (mass parts):
A APTES 10;
B propyl alcohol 60;
C SiO
2Particle 5;
The oxide compound 5 of d cerium;
E deionized water 25;
F acetic acid 3;
G carbon fiber 7;
H polyimide 3;
(2) with carrying out maturation process after the above component mixing, then spray, brush or be immersed in substrate surface, form coating at substrate surface after the deposition, realize the surface anticorrosion processing.
Embodiment 3
(1) prepare following component (mass parts):
A APTES 5;
B propyl alcohol 50;
C SiO
2Particle 3;
The oxide compound 3 of d cerium;
E deionized water 15;
F acetic acid 2;
G carbon fiber 6;
H polyimide 2;
(2) with carrying out maturation process after the above component mixing, then spray, brush or be immersed in substrate surface, form coating at substrate surface after the deposition, realize the surface anticorrosion processing.
Claims (9)
1. the coating scheme of a protective system comprises:
(1) prepare following component (mass parts):
A APTES 1-10;
B propyl alcohol 40-60;
C SiO
2Particle 1-5;
The oxide compound 1-5 of d cerium;
E deionized water 5-25;
F acetic acid 1-3;
G carbon fiber 5-7;
H polyimide 1-3;
(2) with carrying out maturation process after the said components mixing, then spray, brush or be immersed in substrate surface, form coating at substrate surface after the deposition, realize the surface anticorrosion processing.
2. the coating method of described protective system according to claim 1 is characterized in that described SiO
2The particle diameter of particle is the 50-100 nanometer.
3. the coating method of described protective system according to claim 1 is characterized in that described maturation process is to leave standstill at normal temperatures 50-60 hour.
4. the coating method of described protective system according to claim 1 is characterized in that described base material is steel or aluminium.
5. the coating method of described protective system according to claim 1 is characterized in that described base material is aluminium alloy.
6. the coating method of described protective system according to claim 1 is characterized in that heat, Heating temperature is 50 ℃ to 150 ℃, 1 minute to 1 hour heat-up time in described deposition process.
7. the coating method of described protective system according to claim 1 is characterized in that described coat-thickness is 1 micron to 10 microns.
8. the coating method of described protective system according to claim 7 is characterized in that described coat-thickness is 1 micron to 5 microns.
9. the coating method of described protective system according to claim 1 is characterized in that, adopts spraying in the described step (2) or the method for brushing forms coating at substrate surface.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2012105378099A CN102942846A (en) | 2012-12-13 | 2012-12-13 | Coating scheme of anti-corrosion paint |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN2012105378099A CN102942846A (en) | 2012-12-13 | 2012-12-13 | Coating scheme of anti-corrosion paint |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN102942846A true CN102942846A (en) | 2013-02-27 |
Family
ID=47725844
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2012105378099A Pending CN102942846A (en) | 2012-12-13 | 2012-12-13 | Coating scheme of anti-corrosion paint |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN102942846A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103232806A (en) * | 2013-04-22 | 2013-08-07 | 上海华篷防爆科技有限公司 | Coating process of magnesium alloy foil explosion-proof material |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20110062619A1 (en) * | 2009-02-13 | 2011-03-17 | Mayaterials, Inc. | Silsesquioxane derived hard, hydrophobic and thermally stable thin films and coatings for tailorable protective and multi-structured surfaces and interfaces |
| CN102174289A (en) * | 2011-02-25 | 2011-09-07 | 上海交通大学 | Surface anti-corrosion sol for aeronautic aluminum alloy material and treatment method thereof |
| CN102604448A (en) * | 2012-01-20 | 2012-07-25 | 北京北矿锌业有限责任公司 | Material used for metal anti-corrosion coating |
| CN102716849A (en) * | 2012-06-01 | 2012-10-10 | 中国科学院金属研究所 | Protection method applied to aluminum alloy in vanadium battery solution |
| CN102762750A (en) * | 2010-02-19 | 2012-10-31 | 塔塔钢铁荷兰科技有限责任公司 | Strip, sheet or blank suitable for hot forming and process for the production thereof |
-
2012
- 2012-12-13 CN CN2012105378099A patent/CN102942846A/en active Pending
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20110062619A1 (en) * | 2009-02-13 | 2011-03-17 | Mayaterials, Inc. | Silsesquioxane derived hard, hydrophobic and thermally stable thin films and coatings for tailorable protective and multi-structured surfaces and interfaces |
| CN102762750A (en) * | 2010-02-19 | 2012-10-31 | 塔塔钢铁荷兰科技有限责任公司 | Strip, sheet or blank suitable for hot forming and process for the production thereof |
| CN102174289A (en) * | 2011-02-25 | 2011-09-07 | 上海交通大学 | Surface anti-corrosion sol for aeronautic aluminum alloy material and treatment method thereof |
| CN102604448A (en) * | 2012-01-20 | 2012-07-25 | 北京北矿锌业有限责任公司 | Material used for metal anti-corrosion coating |
| CN102716849A (en) * | 2012-06-01 | 2012-10-10 | 中国科学院金属研究所 | Protection method applied to aluminum alloy in vanadium battery solution |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103232806A (en) * | 2013-04-22 | 2013-08-07 | 上海华篷防爆科技有限公司 | Coating process of magnesium alloy foil explosion-proof material |
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| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
| WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20130227 |