CN100447301C - Magnesium alloy phosphate surface modified treatment process - Google Patents
Magnesium alloy phosphate surface modified treatment process Download PDFInfo
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- CN100447301C CN100447301C CNB2006100193245A CN200610019324A CN100447301C CN 100447301 C CN100447301 C CN 100447301C CN B2006100193245 A CNB2006100193245 A CN B2006100193245A CN 200610019324 A CN200610019324 A CN 200610019324A CN 100447301 C CN100447301 C CN 100447301C
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Abstract
The present invention relates to a magnesium alloy phosphate surface modifying treatment method for achieving the purposes of protecting and beautifying magnesium alloy products. The magnesium alloy phosphate surface modifying treatment method comprises the steps of degreasing, acid washing activation, alkali washing, chemical modification, enclosing, water washing and baking; a modifying solution which is used comprises phosphoric acid, barium hydroxide, sodium fluoride, zinc phosphate, etc. The magnesium alloy phosphate surface modifying treatment method has the advantages that a treatment solution utilizing phosphate as a main body is used, chromic acid or cyanide is not used, and thus, pollution can not be caused; because the solution of the entire technical can be repeated under the condition of increasing consumption, resources are greatly economized, and production cost is reduced; compared with anode oxidation technology, the technology reduces cost by 60.5% or so under identical conditions; the technology has the advantages of simplicity, easy formation of automatic production lines and no need of increasing investment for equipment; a chemical conversion film formed by applying the technology greatly improves the adhesive force and corrosion-resisting performance of magnesium alloy components; the optimal control of solution proportioning, heating temperature and treatment time in the technological process of treatment is mastered, and the problems of instability of solutions, nonuniformity of conversion file layers, easy desquamation, etc. in the process of treatment are solved.
Description
Technical field
The present invention relates to a kind of magnesium alloy phosphate surface modified treatment process.
Background technology
Compact day by day and along with various improvised means to its heat radiation and performance such as electromagnetic shielding proposition high requirement, magnesium alloy is little with its proportion, specific tenacity, specific rigidity height, have advantages such as good thermal conductivity, electromagnetic wave shielding, vibration damping and environmental protection, become 21 century the ideal electronic product casing and light vehicle for using material, have broad application prospects at industrial circles such as automobile, computer and aerospace.But because magnesium is as lively as a cricket metal, standard potential is-2.36V that its solidity to corrosion extreme difference has restricted the use of magnesium alloy.Therefore, must carry out suitable surface treatment when magnesium alloy uses as structured material, to improve its solidity to corrosion, this performance advantage to performance magnesium and magnesium alloy has important practical sense.At present, according to filming condition, magnesium alloy surface treatment can reduce chemical membrane and anode oxidation film-forming two big classes, but, the anode oxidation film-forming treatment technology exists complex process, higher, the very difficult validity of treatment solution and the problems such as homoeostasis of treatment solution temperature of keeping of cost, therefore also is difficult to promote the use of.The equipment that chemical conversion technology need be used is simple, less investment, and easily operation, cost is low, and it is generally as the bottom of application, to strengthen the tack of application.Owing in film process, do not use power supply, thus do not exist because the drawback that the thicknesses of layers that the electric force lines distribution inequality causes is inhomogeneous and the deep hole place can not depositional coating, so long as the surface that electrolytic solution can arrive can both obtain the uniform conversion film of thickness.Usually; chromium series elements reagent is all adopted in the magnesium alloy chemical surface treatment; handle among the No.20 (correction type chromic acid processing procedure) as the chemical modification of No. the 4676842nd, United States Patent (USP) and U.S. Dow chemical company; all adopt chromatedsolution that metal is carried out chemical modification, prevent that with the protectiveness epithelium that forms one deck densification metal is corroded.But contain the high pollution chemical substance Cr that promising Fan Saier pact is forbidden in the formed epithelium
3+, the recovery of magnesium alloy is in the future caused difficulty.In addition, contain Cr in the treatment trough
3+The toxic gas that solution volatilized, threaten for the health of operator, and the discharging of the solution in the treatment trough also needs to carry out wastewater treatment, but Cr
3+Be not easy sedimentation, will cause the cost of wastewater treatment to improve.In a word, the surface treatment of magnesium alloy chromic salt chemistry all has in various degree harm to human body and environment.Along with the increase day by day of magnesium-alloy material demand, exploitation to environment and operator do not have the technology of harm and treatment solution, realization " green surface treatment " will be a main developing direction from now on.Up to now domestic and international many scholars are chemical method for treating surface at the research Chrome-free also, are doing a lot of work aspect the potassium permanganate system Chrome-free conversion film as Japanese scholar Mei Yuanbo is capable etc.; David Hawke carries out phosphoric acid salt-permanganate to magnesium alloy AM60B to be handled, and obtains one deck conversion film at Mg alloy surface, discovers, the color of film and thickness are very responsive to the treatment time; M.A.Gonzalez etc. have studied the stannate conversion film low-cost, that pollution is light, and the solid solution of ZC71 magnesium alloy, shrend, temper after pre-treatments such as pickling are immersed stannate with sample again, can be formed the chemical conversion film of 2～5 μ m on the surface; Add rare earth element and also can form protective membrane, A.L.Rudd etc. have studied the film forming characteristics of nitrate on the WE43 magnesium alloy of lanthanum, praseodymium; A.K.Sharma has studied without soaking zinc, the technology of direct chemical nickel plating on magnesium; The Yin Jianjun research of Gansu Polytechnical Univ is directly zinc-plated on Mg alloy surface; The Huo Hongwei of Dai Changsong, the Chinese Academy of Sciences etc. has studied chemical nickel plating on the magnesium, but basal body binding force is poor, so zinc is soaked in adding in the centre.These Chrome-frees are that the chemical conversion film of treatment process generation is thinner, solidity to corrosion, sticking power are all lower, so people are seeking a kind of corrosion resisting property that can satisfy environmental requirement, improve magnesium alloy in recent years always, certain commercial value is arranged again, can save the magnesium and the magnesium alloy surface treatment of the energy again.
Summary of the invention
The purpose of this invention is to provide a kind of magnesium alloy phosphate surface modified treatment process, it can satisfy environmental requirement, improves the performances such as corrosion-resistant, sticking power of magnesium alloy, can save the energy again.
The present invention is achieved like this, and its operation steps is: (1) is at first with magnesium alloy polishing, material loading; (2) carry out pretreatment technology: product is immersed be equipped with in the degreasing tank of 5%～10% sodium hydroxide, be heated to 80～98 ℃ by the ultrasonic wave effect after 20～30 minutes, enter in the first distilled water washing bath,, take out and use hot blast drying at room temperature with ultrasonic wave effect 20～50 seconds; (3) immersion fills in the pickling tank of hydrofluoric acid, ethylene glycol solution then, at room temperature with ultrasonic wave effect 1～2.5 minute, enters after the pickling in the after-fractionating water washing bath, equally at room temperature with ultrasonic wave effect 20～50 seconds, takes out and uses hot blast drying; (4) immersion is equipped with in the alkaline bath of 20%～30% sodium hydroxide again, at room temperature with ultrasonic wave effect 25～30 minutes, immerses then in the triply distilled water washing bath, and room temperature ultrasonic cleaned 20～50 seconds, takes out and uses hot blast drying; (5) carry out chemical membrane technology: product is put into the groove that fills phosphoric acid, hydrated barta, Sodium Fluoride, zinc phosphate, sodium chlorate modification treatment soln, be heated to 80～100 ℃, with ultrasonic wave effect 10～30 minutes, put into the 4th distilled water washing bath cleaned by ultrasonic vibration then, take out hot blast drying; (6) carried out sealing treatment 25～35 minutes in the sodium silicate aqueous solution of 50～65 ℃ of temperature of immersion, take out at once with hot blast drying and blanking.
By adopting method of the present invention and prescription, be that the main characteristic of the chemical conversion rete that obtains of example is as follows with the AZ91D magnesium alloy materials:
Chemical conversion rete outward appearance: white evenly, and is moist;
Chemical conversion thicknesses of layers: 80～110um;
Chemical conversion rete sticking power: 40.33kg/cm
2Magnesium alloy substrate sticking power is 17.5kg/cm
2, visible phosphate chemical transforms the sticking power that rete can obviously improve magnesium alloy;
Chemical conversion rete resistance to salt(spray)fog: after 33 hours, corrosion just appears, magnesium alloy substrate, general corrosion just appearred in 8 hours in conversion film zinc-plated, nickel plating, and visible phosphate chemical transforms the salt fog resistance performance that rete has improved magnesium alloy parts greatly;
Chemical conversion rete moisture resistance: behind the 60h, corrosion just occurs, general corrosion just appears in magnesium alloy substrate after 7 hours, and visible rete improves the moisture resistance of magnesium alloy parts greatly.
Advantage of the present invention is: 1, this technology is the treatment soln based on phosphoric acid salt, does not use chromic acid or prussiate, and is pollution-free, satisfies the requirement of environmental protection and Sustainable development in actual production; Solved the harm in various degree that chromate treatment solution contains in the old treatment process chromium or heavy non-ferrous metal element cause environment and human body; 2, the solution of a whole set of technology can be reused appending under the situation of loss, and this just saves resource widely, has reduced production cost, compares with anode oxidation process, under identical condition, can reduce about 60.5% cost; 3, this technical matters is simple, easily forms automatic production line, and does not need big facility investment, and it is short to form the production capacity time, can adapt to current social competition needs, improves enterprise competitiveness; 4, the chemical conversion film that uses this technology to form has improved sticking power, the corrosion resistance nature of magnesium alloy parts greatly, compare other chemical film forming method (as zinc-plated, nickel plating, potassium permanganate and stannate etc.) of Chrome-free system, the phosphate chemical film forming can improve the erosion resistance of magnesium alloy more; 5, grasp the control of solution ratio in the treatment process process, Heating temperature and the optimization in treatment time, overcome solution instability in the treating processes, transformed inhomogeneous, the easy difficult problem such as come off of rete.
Embodiment
The present invention is further illustrated below in conjunction with embodiment: material is a magnesium alloy electric hand drill handpiece case
Obtain solution at first: at room temperature place in the beakers with accurate sodium hydroxide 80 grams of electronic analytical balance, the a spot of distilled water of adding stirs in advance medicine is fully dissolved in beaker, pour into then in 1000 milliliters of measuring bottles, correctly be added into the skim soln that graticule promptly makes 1 liter with distilled water.Equally accurately take by weighing 50% hydrofluoric acid 80 grams, ethylene glycol 32 grams in addition and place beaker with electronic analytical balance, adding a small amount of distilled water stirring in beaker fully dissolves medicine, after pour in 1000 milliliters the measuring bottle, adding distil water to graticule promptly makes 1 liter acid-wash activation solution.The weighing sodium hydroxide that uses the same method then 100～180 grams are mixed with 1 liter soda-wash solution.Take by weighing phosphoric acid 60～100 grams more respectively, hydrated barta 40～60 grams, Sodium Fluoride 1～4 gram, zinc phosphate 2～6 grams, sodium chlorate 3～8 grams are mixed with 1 liter of solution, take by weighing 1 liter of solution of water glass 18 gram preparations at last.
Technical process operation then:
1, with electric hand drill handpiece case material loading.
2, put into 80～98 ℃ of degreasing tanks,, make grease and basic solution and surfactant generation saponification reaction and emulsion reaction and be dissolved in the water,, can obviously see the piece surface light that becomes to reach the purpose of degreasing with ultrasonic wave effect 20～30 minutes.Action of ultrasonic waves that each operation adopts is that on the one hand vibration makes solution particulates active, makes it with the metallic surface chemical reaction to take place fully in present method; Particulate in the solution and metal parts surface is vibrated, and the impurity particle on particulate vibration and the impact metallic surface makes it be subjected to shearing force and separates from the metallic surface, thereby reaches the purpose of clean metal piece surface.Put into first washing bath, at room temperature removed basic solution and the grease molecule that remains on the Mg alloy surface in 20～50 seconds, take out and use hot blast drying by ultrasonic cleaning.
3, immerse in the groove fill the acidic activated solution of before being prepared, at room temperature with ultrasonic wave effect 1～2.5 minute, the microetch metallic surface to be to remove the oxide compound that product surface generates, in addition can also in degreasing after remain in alkaline matter on the product.Enter in second washing bath, at room temperature removed acidic solution and the oxide particle that remains on the Mg alloy surface in 20～50 seconds, take out and use hot blast drying by ultrasonic cleaning.
4, immersion is equipped with in the alkaline bath of sodium hydroxide, and at room temperature with ultrasonic wave effect 25～30 minutes, neutralization remains in the lip-deep acidic substance of magnesium-alloy material.Enter the 3rd washing bath, act on the identical time, hot blast drying.
5, the modified solution that will before prepare is heated to 80～100 ℃, and magnesium alloy parts is put into, and makes piece surface form the protectiveness chemical conversion film of one deck densification in 10～30 minutes by the ultrasonic wave effect.Immerse after the modification in the 4th washing bath, at room temperature removed residual chemical reagent on the piece surface in 20～50 seconds, take out hot blast drying by ultrasonic cleaning.
6, immerse at last in 50～65 ℃ of sodium silicate aqueous solutions and carried out sealing treatment 25～35 minutes, make the phosphate conversion film even compact of generation, take out at once with hot blast drying and blanking.
Claims (4)
1, a kind of magnesium alloy phosphate surface modified treatment process is characterized in that operation steps is: (1) is at first with magnesium alloy polishing, material loading; (2) carry out pretreatment technology: product is immersed be equipped with in the degreasing tank of 5%～10% sodium hydroxide, be heated to 80～98 ℃ of temperature, after 20～30 minutes, enter in the first distilled water washing bath by the ultrasonic wave effect, at room temperature, take out and use hot blast drying with ultrasonic wave effect 20～50 seconds; (3) immersion fills in the pickling tank of hydrofluoric acid, ethylene glycol solution, at room temperature with ultrasonic wave effect 1～2.5 minute, enters after the pickling in the after-fractionating water washing bath, equally at room temperature with ultrasonic wave effect 20～50 seconds, takes out and uses hot blast drying; (4) immersion is equipped with in the alkaline bath of 20%～30% sodium hydroxide, at room temperature with ultrasonic wave effect 25～30 minutes, immerses then in the triply distilled water washing bath, and room temperature ultrasonic cleaned 20～50 seconds, takes out and uses hot blast drying; (5) carry out chemical membrane technology: product is put into the groove that fills the modification treatment soln, the concentration of modification treatment solution is phosphoric acid 60～100 grams in 1 liter of solution, hydrated barta 40～60 grams, Sodium Fluoride 1～4 gram, zinc phosphate 2～6 grams, sodium chlorate 3～8 grams, be heated to 80～100 ℃, with ultrasonic wave effect 10～30 minutes, put into the 4th distilled water washing bath cleaned by ultrasonic vibration, take out hot blast drying; (6) immerse in the sodium silicate aqueous solution of 50～65 ℃ of temperature and carried out sealing treatment 25～35 minutes, water glass solubility is that 1 liter of solution contains 18 gram water glass, takes out at once with hot blast drying and blanking.
2, magnesium alloy phosphate surface modified treatment process according to claim 1 is characterized in that sodium hydroxide 80 grams in 1 liter of skim soln.
3, magnesium alloy phosphate surface modified treatment process according to claim 1 is characterized in that the hydrofluoric acid in the pickling tank, the concentration of ethylene glycol solution are that 1 liter of solution contains 50% hydrofluoric acid 80 grams, ethylene glycol 32 grams.
4, magnesium alloy phosphate surface modified treatment process according to claim 1 is characterized in that sodium hydroxide 100～180 is restrained the soda-wash solution that is mixed with 1 liter.
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| CNB2006100193245A CN100447301C (en) | 2006-06-06 | 2006-06-06 | Magnesium alloy phosphate surface modified treatment process |
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| CN100447301C true CN100447301C (en) | 2008-12-31 |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11518960B2 (en) | 2016-08-24 | 2022-12-06 | Ppg Industries Ohio, Inc. | Alkaline molybdenum cation and phosphonate-containing cleaning composition |
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| CN102115880B (en) | 2009-12-31 | 2015-10-14 | 汉高股份有限及两合公司 | The surface treating composition of light metal or its alloy and solution and surface treatment method |
| CN103898577A (en) * | 2013-06-03 | 2014-07-02 | 无锡市锡山区鹅湖镇荡口青荡金属制品厂 | Pretreatment process of electroplating chromium on surface of magnesium alloy die casting |
| CN103668163B (en) * | 2013-10-31 | 2016-08-31 | 沈阳工业大学 | A kind of magnesium alloy die casting process for surface preparation |
| CN104561980A (en) * | 2015-01-06 | 2015-04-29 | 南昌大学 | Surface treatment method for magnesium alloy |
| CN106222679A (en) * | 2016-08-29 | 2016-12-14 | 东莞宜安科技股份有限公司 | A kind of magnesium alloy die casting surface treatment method |
| CN111041265B (en) * | 2019-11-11 | 2021-07-02 | 北京科技大学 | Preparation of degradable magnesium alloy sliding sleeve fracturing ball and method for controlling degradation rate |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1993009266A1 (en) * | 1991-11-01 | 1993-05-13 | Henkel Corporation | Phosphate conversion coating composition and process |
| EP0723603A1 (en) * | 1993-10-15 | 1996-07-31 | Circle-Prosco, Inc. | Conversion coatings for metal surfaces |
| CN1219982A (en) * | 1996-05-28 | 1999-06-16 | 汉克尔股份两合公司 | Zinc phosphating process with integrated subsequent passivation |
| CN1300878A (en) * | 1999-12-14 | 2001-06-27 | 三井金属矿业株式会社 | Chemical treating liquid for magnesium alloy containing aluminium, high corrosionproofing magnesium alloy products and manufacture thereof |
-
2006
- 2006-06-06 CN CNB2006100193245A patent/CN100447301C/en not_active Expired - Fee Related
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1993009266A1 (en) * | 1991-11-01 | 1993-05-13 | Henkel Corporation | Phosphate conversion coating composition and process |
| EP0723603A1 (en) * | 1993-10-15 | 1996-07-31 | Circle-Prosco, Inc. | Conversion coatings for metal surfaces |
| CN1219982A (en) * | 1996-05-28 | 1999-06-16 | 汉克尔股份两合公司 | Zinc phosphating process with integrated subsequent passivation |
| CN1300878A (en) * | 1999-12-14 | 2001-06-27 | 三井金属矿业株式会社 | Chemical treating liquid for magnesium alloy containing aluminium, high corrosionproofing magnesium alloy products and manufacture thereof |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11518960B2 (en) | 2016-08-24 | 2022-12-06 | Ppg Industries Ohio, Inc. | Alkaline molybdenum cation and phosphonate-containing cleaning composition |
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