CN105296993A - Stripping-resisting aluminum alloy corrosion resisting lifting sol and preparation method thereof - Google Patents
Stripping-resisting aluminum alloy corrosion resisting lifting sol and preparation method thereof Download PDFInfo
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- CN105296993A CN105296993A CN201510711918.1A CN201510711918A CN105296993A CN 105296993 A CN105296993 A CN 105296993A CN 201510711918 A CN201510711918 A CN 201510711918A CN 105296993 A CN105296993 A CN 105296993A
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C22/05—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
- C23C22/06—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
- C23C22/48—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 not containing phosphates, hexavalent chromium compounds, fluorides or complex fluorides, molybdates, tungstates, vanadates or oxalates
- C23C22/56—Treatment of aluminium or alloys based thereon
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- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C2222/00—Aspects relating to chemical surface treatment of metallic material by reaction of the surface with a reactive medium
- C23C2222/20—Use of solutions containing silanes
Abstract
The invention discloses stripping-resisting aluminum alloy corrosion resisting lifting sol. The stripping-resisting aluminum alloy corrosion resisting lifting sol is prepared from, by weight, 2-3 parts of ricinoleic acid, 10-12 parts of nanometer titania, 0.8-1 part of stearic acid, 0.2-0.4 part of sodium dodecyl benzene sulfonate, 10-18 parts of dodecafluoroheptyl-propyl-trimethoxysilane, 20-30 parts of hydrogen containing silicone oil, 0.7-1 part of 25%-28% ammonium hydroxide, 90-100 parts of silane coupling agent KH5601-2,2,3-dimethylaniline, 0.6-1 part of ammonium persulfate, 1-2 parts of tetradecane binary acid, 2-3 parts of inositol, 0.7-1 part of sodium lignin sulfonate, 0.2-0.3 part of ethylene carbonate, 1.3-2 parts of tetrabutylammonium bromide and 0.06-0.1 part of polytetrafluoroethylene. According to the sol, a stable coating is formed on the surface of aluminum alloy, the binding performance of the coating and a base material is high, peel strength is high, weather fastness is good, and comprehensive performance is excellent.
Description
Technical field
The present invention relates to technical field of aluminum alloy technology, particularly relate to a kind of antistripping corrosive protection of aluminium alloy lift colloidal sol and preparation method thereof.
Background technology
As everyone knows, contact angle (CA) is greater than 150 ° and the surface that roll angle (SA) is less than 10 ° is called super hydrophobic surface by us.In recent years, super hydrophobic material is widely used in fundamental research, daily life and industrial production with the performance of its uniqueness, can be used for the fields such as Metal surface anti-corrosion, fluid drag-reduction, waterproof, antifouling and automatically cleaning, organic-inorganic nanocomposite is as the field of emerging emergence, in super-hydrophobic composite organic-inorganic material system, critical positions is occupied with its superior performance, main with organic and inorganic thing for raw material, adopt proper method to make it to be composited by chemical bond within the scope of micro-/ nano.Wherein, inorganic nano-particle Chang Zuowei packing material, obtains micro-/ nano secondary structure with organism compound, gives matrix material superhydrophobic property;
Metal is under the effect of surrounding medium (especially water and air), and the destruction produced due to chemical reaction, electrochemical reaction or physical dissolution is exactly corrosion of metal, is the inverse process of the spontaneous a kind of metallurgy carried out silently.The industrial media such as the physical environments such as air, soil, seawater and microorganism and acid, alkali, salt, combustion gas all likely cause corrosion of metal.The harm that metallic corrosion brings, throughout the every field of national economy, comprises chemical industry, the energy, machinery, aerospace, information, agricultural, ocean exploitation and Infrastructure etc.As long as use the place of metallic substance, all more or less there is etching problem.The etching problem of metallic substance and study effective aseptic technic oneself becomes the problem of can not ignore in current Materials Science and Engineering field;
Polyaniline has cheaper starting materials and is easy to get, synthesizes the feature such as simple and be counted as the high-performance impregnating material of a new generation.After the polyaniline film proposing first to adopt electrochemical method to prepare from DeBerry in 1985 has passivation on stainless steel surface, polyaniline has become a new focus in the research and development in anticorrosion.Although the anticorrosion mechanism of polyaniline is not also completely understood, the antiseptic property of the excellence that polyaniline shows is mathematical, and therefore, people still proceed further investigation to it.At present, the research for polyaniline is mainly divided into two aspects: one is on existing Research foundation, continues p-poly-phenyl amine anticorrosion mechanism and carries out comparatively deep research and exploitation; Two is the barrier propterties carrying out to improve further polyaniline coating by all means.
Summary of the invention
The object of the invention is exactly the defect in order to make up prior art, provides a kind of antistripping corrosive protection of aluminium alloy to lift colloidal sol and preparation method thereof.
The present invention is achieved by the following technical solutions:
A kind of antistripping corrosive protection of aluminium alloy lift colloidal sol, it is made up of the raw material of following weight parts:
Ricinolic acid 2-3, nano titanium oxide 10-12, stearic acid 0.8-1, Sodium dodecylbenzene sulfonate 0.2-0.4, ten difluoro heptyl propyl trimethoxy silicane 10-18, ammoniacal liquor 0.7-1, the silane coupling agent KH5601-2 of containing hydrogen silicone oil 20-30,25-28%, 23 dimethyl aniline 90-100, ammonium persulphate 0.6-1, tetradecane diprotic acid 1-2, nucite 2-3, sodium lignosulfonate 0.7-1, NSC 11801 0.2-0.3, Tetrabutyl amonium bromide 1.3-2, tetrafluoroethylene 0.06-0.1;
A preparation method for described antistripping corrosive protection of aluminium alloy lift colloidal sol, comprises the following steps:
(1) join in dehydrated alcohol by above-mentioned stearic acid, stirring and dissolving, described dehydrated alcohol and stearic envelope-bulk to weight ratio are 25-30:1;
(2) above-mentioned nano titanium oxide is joined its weight 10-12 doubly, in the ethanolic soln of 60-65%, magnetic agitation is even, adds above-mentioned stearic ethanolic soln, magnetic agitation 3-4 hour, dry at 120-125 DEG C, grinding, obtains stearic acid modified titanium dioxide;
(3) joined in 10-14 times of deionized water by sodium lignosulfonate last time, stir, add tetradecane diprotic acid, raised temperature is 60-65 DEG C, insulated and stirred 5-7 minute, is dispersion liquid;
(4) 20-30% of above-mentioned Sodium dodecylbenzene sulfonate weight is got, join in 200-210 times of deionized water, stir, add above-mentioned dispersion liquid, stir, add above-mentioned ten difluoro heptyl propyl trimethoxy silicanes, containing hydrogen silicone oil, 1000-1200 rev/min is stirred 2-3 hour, drip the Karstedt catalyzer of above-mentioned system weight 1-2%, stirring reaction 1-2 hour, obtains fluorinated silicone oil;
(5) above-mentioned ricinolic acid is joined in nucite, stir, add NSC 11801, insulated and stirred 10-20 minute at 80-90 DEG C, drip the sulfuric acid of 96-98%, adjustment PH is 1-2, reduction temperature is 60-70 DEG C, insulation reaction 1-2 hour, adds tetrafluoroethylene, be stirred to normal temperature, obtain Preblend;
(6) remaining Sodium dodecylbenzene sulfonate is got, join in its weight 70-100 times deionized water, stir, drip the ammoniacal liquor of above-mentioned 25-28%, after dropwising, add 23 dimethyl aniline, stir, raised temperature is 50-60 DEG C, adds above-mentioned stearic acid modified titanium dioxide, insulated and stirred 10-20 minute, reduction temperature is 30-35 DEG C, add ammonium persulphate, insulated and stirred 10-12 hour, add above-mentioned Preblend, stir, suction filtration, vacuum-drying 30-40 minute at 90-100 DEG C, obtains polymer modification titanium dioxide;
(7) join in fluorinated silicone oil by above-mentioned polymer modification titanium dioxide, add silane coupling agent KH560, stir, adjustment PH is 5-6, and add each raw material of residue, insulated and stirred 3-4 hour at 50-60 DEG C, obtains composite modified colloidal sol.
Described a kind of corrosive protection of aluminium alloy lift colloidal sol, the using method of this colloidal sol is:.
Advantage of the present invention is:
The film of gel formation of the present invention has good water resisting property:
Stearic acid contain a large amount of-COOH group, dehydration reaction can be there is with surface of inorganic particles-OH, also hydrophobicity-CH3 group can be introduced for TiO2, but modified TiO2 is poor at body surface sticking power, easy generation obscission, containing hydrogen silicone oil has good chemical stability and high hydrophobicity energy, can interact with inorganic particulate and form abundant microtexture, ten difluoro heptyl propyl trimethoxy silicanes contain hydrophobicity-CH3 and hydrolyzable-OCH3, it is utilized to fluoridize containing hydrogen silicone oil, containing hydrogen silicone oil generation dehydrogenation coupling reaction can be made, more excellent mechanical property is possessed under crosslinked action, make compound coating more stable, in addition, the hydrophobic methyl introduced also can increase the hydrophobic effect of coating,
The film of gel formation of the present invention has good non-corrosibility:
Micro/nano structure of the present invention has effectively intercepted air in water and has contacted with the direct of aluminium flake substrate, and the amount of oxygen making aluminium flake surface participate in reaction reduces, thus slow down the generation of aluminium flake surface film oxide; On the other hand, the reticulated structure formed by Si-O had in compound coating is combined with aluminium flake intimate surface, the fluoroalkyl of hydrophobic then points to corrodibility NaCl solution one end, in addition, the modifying titanium dioxide of compound coating surface compact possesses abundant surface microstructure and has low surface energy, and this plays a key effect to the protection against corrosion of coating;
The present invention introduces polyaniline in gel, make the reduction reaction of oxygen from the metal/corrosive medium interfacial migration of routine to polymkeric substance/corrosive medium interface, decrease the generation at metal/corrosive medium surface OH-, prevent the rising of metallic surface pH, serve good corrosion mitigating effect, effectively prevent the degraded of coating, peel off;
Colloidal sol of the present invention forms stable film in aluminum alloy surface, and the cohesiveness of this film and base material is strong, and peel strength is high, good weatherability, and over-all properties is superior.
Embodiment
A kind of antistripping corrosive protection of aluminium alloy lift colloidal sol, it is made up of the raw material of following weight parts:
Ricinolic acid 2, nano titanium oxide 10, stearic acid 0.8, Sodium dodecylbenzene sulfonate 0.2, ten difluoro heptyl propyl trimethoxy silicane 10, the ammoniacal liquor 0.7 of containing hydrogen silicone oil 20,25%, silane coupling agent KH5601,2,3 xylidines 90, ammonium persulphate 0.6, tetradecane diprotic acid 1, nucite 2, sodium lignosulfonate 0.7, NSC 11801 0.2, Tetrabutyl amonium bromide 1.3, tetrafluoroethylene 0.06;
A preparation method for described antistripping corrosive protection of aluminium alloy lift colloidal sol, comprises the following steps:
(1) join in dehydrated alcohol by above-mentioned stearic acid, stirring and dissolving, described dehydrated alcohol and stearic envelope-bulk to weight ratio are 25:1;
(2) above-mentioned nano titanium oxide is joined its weight 10 times, 60% ethanolic soln in, magnetic agitation is even, adds above-mentioned stearic ethanolic soln, magnetic agitation 3 hours, dries at 120 DEG C, and grinding, obtains stearic acid modified titanium dioxide;
(3) joined in 10 times of deionized waters by sodium lignosulfonate last time, stir, add tetradecane diprotic acid, raised temperature is 60 DEG C, and insulated and stirred 5 minutes is dispersion liquid;
(4) 20% of above-mentioned Sodium dodecylbenzene sulfonate weight is got, join in 200 times of deionized waters, stir, add above-mentioned dispersion liquid, stir, add above-mentioned ten difluoro heptyl propyl trimethoxy silicanes, containing hydrogen silicone oil, 1000 revs/min are stirred 2 hours, drip the Karstedt catalyzer of above-mentioned system weight 1%, stirring reaction 1 hour, obtains fluorinated silicone oil;
(5) above-mentioned ricinolic acid is joined in nucite, stir, add NSC 11801, insulated and stirred 10 minutes at 80 DEG C, drip the sulfuric acid of 96%, regulate PH to be 1, reducing temperature is 60 DEG C, insulation reaction 1 hour, add tetrafluoroethylene, be stirred to normal temperature, obtain Preblend;
(6) get remaining Sodium dodecylbenzene sulfonate, join in its weight 70 times of deionized waters, stir, drip the ammoniacal liquor of above-mentioned 25%, after dropwising, add 2,3 xylidines, stir, raised temperature is 50 DEG C, adds above-mentioned stearic acid modified titanium dioxide, insulated and stirred 10 minutes, reducing temperature is 30 DEG C, adds ammonium persulphate, insulated and stirred 10 hours, adds above-mentioned Preblend, stirs, suction filtration, at 90 DEG C, vacuum-drying 30 minutes, obtains polymer modification titanium dioxide;
(7) join in fluorinated silicone oil by above-mentioned polymer modification titanium dioxide, add silane coupling agent KH560, stir, regulate PH to be 5, add each raw material of residue, at 50 DEG C, insulated and stirred 3 hours, obtains composite modified colloidal sol.
Described a kind of corrosive protection of aluminium alloy lift colloidal sol, the using method of this colloidal sol is:.
Performance test:
Water-intake rate: according to the method described above surface treatment agent of the present invention is coated on the aluminum alloy surface being of a size of 5cm × 6cm, soaks 48h in the deionized water of 25 DEG C, and recording water-intake rate is 10.0%;
Sticking power: 1 grade;
Erosion resistance: neutral salt spray test 72 hours, be corroded area 2.0%;
Hardness: 3H.
Claims (3)
1. an antistripping corrosive protection of aluminium alloy lift colloidal sol, it is characterized in that, it is made up of the raw material of following weight parts:
Ricinolic acid 2-3, nano titanium oxide 10-12, stearic acid 0.8-1, Sodium dodecylbenzene sulfonate 0.2-0.4, ten difluoro heptyl propyl trimethoxy silicane 10-18, ammoniacal liquor 0.7-1, the silane coupling agent KH5601-2 of containing hydrogen silicone oil 20-30,25-28%, 23 dimethyl aniline 90-100, ammonium persulphate 0.6-1, tetradecane diprotic acid 1-2, nucite 2-3, sodium lignosulfonate 0.7-1, NSC 11801 0.2-0.3, Tetrabutyl amonium bromide 1.3-2, tetrafluoroethylene 0.06-0.1.
2. a preparation method for antistripping corrosive protection of aluminium alloy lift colloidal sol as claimed in claim 1, is characterized in that, comprise the following steps:
(1) join in dehydrated alcohol by above-mentioned stearic acid, stirring and dissolving, described dehydrated alcohol and stearic envelope-bulk to weight ratio are 25-30:1;
(2) above-mentioned nano titanium oxide is joined its weight 10-12 doubly, in the ethanolic soln of 60-65%, magnetic agitation is even, adds above-mentioned stearic ethanolic soln, magnetic agitation 3-4 hour, dry at 120-125 DEG C, grinding, obtains stearic acid modified titanium dioxide;
(3) joined in 10-14 times of deionized water by sodium lignosulfonate last time, stir, add tetradecane diprotic acid, raised temperature is 60-65 DEG C, insulated and stirred 5-7 minute, is dispersion liquid;
(4) 20-30% of above-mentioned Sodium dodecylbenzene sulfonate weight is got, join in 200-210 times of deionized water, stir, add above-mentioned dispersion liquid, stir, add above-mentioned ten difluoro heptyl propyl trimethoxy silicanes, containing hydrogen silicone oil, 1000-1200 rev/min is stirred 2-3 hour, drip the Karstedt catalyzer of above-mentioned system weight 1-2%, stirring reaction 1-2 hour, obtains fluorinated silicone oil;
(5) above-mentioned ricinolic acid is joined in nucite, stir, add NSC 11801, insulated and stirred 10-20 minute at 80-90 DEG C, drip the sulfuric acid of 96-98%, adjustment PH is 1-2, reduction temperature is 60-70 DEG C, insulation reaction 1-2 hour, adds tetrafluoroethylene, be stirred to normal temperature, obtain Preblend;
(6) remaining Sodium dodecylbenzene sulfonate is got, join in its weight 70-100 times deionized water, stir, drip the ammoniacal liquor of above-mentioned 25-28%, after dropwising, add 23 dimethyl aniline, stir, raised temperature is 50-60 DEG C, adds above-mentioned stearic acid modified titanium dioxide, insulated and stirred 10-20 minute, reduction temperature is 30-35 DEG C, add ammonium persulphate, insulated and stirred 10-12 hour, add above-mentioned Preblend, stir, suction filtration, vacuum-drying 30-40 minute at 90-100 DEG C, obtains polymer modification titanium dioxide;
(7) join in fluorinated silicone oil by above-mentioned polymer modification titanium dioxide, add silane coupling agent KH560, stir, adjustment PH is 5-6, and add each raw material of residue, insulated and stirred 3-4 hour at 50-60 DEG C, obtains composite modified colloidal sol.
3. a kind of corrosive protection of aluminium alloy lift colloidal sol according to claim 1, it is characterized in that, the using method of this colloidal sol is:
Be immersed in by aluminium flake clean for surface treatment in this composite modified colloidal sol, carry out Best-Effort request plated film, namely repeatable operation obtains certain thickness uniform thin film, under being then placed in room temperature after dry 20-30min, under 125-130 DEG C of condition, cures 25-30min.
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
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| CN116479677A (en) * | 2023-04-28 | 2023-07-25 | 东莞市众智达生物新材料有限公司 | Filler with distillers' grains waste as raw material and preparation method and application thereof |
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| CN101962514A (en) * | 2010-09-27 | 2011-02-02 | 复旦大学 | High-durability super-hydrophobic self-cleaning coating material and preparation method thereof |
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| CN116479677A (en) * | 2023-04-28 | 2023-07-25 | 东莞市众智达生物新材料有限公司 | Filler with distillers' grains waste as raw material and preparation method and application thereof |
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Application publication date: 20160203 |