CN105132965A - Alkaline plating solution for platinum electroplating and electroplating method adopting alkaline plating solution - Google Patents
Alkaline plating solution for platinum electroplating and electroplating method adopting alkaline plating solution Download PDFInfo
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- CN105132965A CN105132965A CN201510604424.3A CN201510604424A CN105132965A CN 105132965 A CN105132965 A CN 105132965A CN 201510604424 A CN201510604424 A CN 201510604424A CN 105132965 A CN105132965 A CN 105132965A
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- plating solution
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- electroplate liquid
- electroplating
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Abstract
The invention discloses an alkaline plating solution for platinum electroplating and an electroplating method adopting the alkaline plating solution. The plating solution comprises 10-20 g/L of dipotassium platinate calculated as platinum, 20-60 g/L of potassium hydroxide or sodium hydroxide and 100-300 mg/L of sodium glutamate. According to the invention, the dipotassium platinate is used as platinum main salt, the sodium glutamate is used as a brightener, and the potassium hydroxide or sodium hydroxide is added to adjust the plating solution to be alkaline, so that an obtained plating solution has better dispersion force and deep plating capacity, and is high in cathode current efficiency and excellent in performance. A plating layer obtained by electroplating through the plating solution under alkaline conditions is low in porosity, high in brightness and good in quality.
Description
Technical field
The present invention relates to electroplatinizing technical field, particularly relate to a kind of alkali plating solution and electro-plating method thereof of electroplatinizing.
Background technology
The superior performance of platinum, purposes is very extensive.In bullion industry, main as ornament and artwork.In chemical industry, in order to manufacture the catalyzer of senior chemical ware, platinum crucible, electrode and acceleration chemical reaction velocity.Platinum iridium alloy is the material manufacturing fountain pen nib.Especially in the automotive industry, the effect of platinum in vent gas treatment etc. can not be substituted, and consumption almost accounts for the half of platinum industry consumption.Due to.But platinum scarcity of resources, expensive, constrain the application of platinum electrode, thus replace pure platinum goods with platinum plated materials, both reduced costs, there is again the premium properties of platinum anode.
Chinese patent CN101016639 discloses a kind of platinum titanium basal body electric plating platinum coating technique, and this technique adopts Platinic chloride as electroplate liquid.Although this technique technique is comparatively simple, the current efficiency of this plating solution is lower, the poor-performing of plating solution, and the quality of coating is not good yet.
Summary of the invention
In view of this, one aspect of the present invention provides a kind of alkali plating solution of electroplatinizing, and the plating solution performance of this plating solution is better, and the quality of coating using this plating solution to obtain is higher.
An electroplate liquid for alkaline platinum plating, comprises in platinum 10 ~ 20g/L hexahydroxy-potassium platinate, 20 ~ 60g/L potassium hydroxide or sodium hydroxide and 100 ~ 300mg/L Sodium Glutamate.
Wherein, comprise further in platinum 14g/L hexahydroxy-potassium platinate, 50g/L potassium hydroxide or sodium hydroxide and 180mg/L Sodium Glutamate.
In this electroplate liquid, select hexahydroxy-potassium platinate to be main salt, add sodium hydroxide or potassium hydroxide and make plating solution be alkalescence.Hexahydroxy-potassium platinate under alkaline condition with Pt (OH)
6 2-form be present in plating solution.The platinum salt of hexahydroxy-potassium platinate has higher cathode efficiency.
Take Sodium Glutamate as brightening agent.Sodium Glutamate contains two amino and a carboxyl, and amino and carboxyl can be formed with platinum and fit in platinum complex ion, and galvanic deposit produces the coating of comparatively light.100 ~ 300mg/L Sodium Glutamate can make coating have entire bright.
Except mentioned component, the present invention also can select suitable amounts other in this area the additive commonly used, such as conductive agent, etc. conven-tional adjuvants, these all can not damage the characteristic of coating.
The present invention provides a kind of electro-plating method, the better performances of the electroplate liquid that the method adopts on the other hand, higher according to quality of coating prepared by the method.
The above-mentioned plating solution electric plating method of a kind of use, comprises the following steps:
(1) electroplate liquid is prepared: in water, dissolve each feed composition form electroplate liquid, described often liter of electroplate liquid contains in platinum 10 ~ 20g hexahydroxy-potassium platinate, 20 ~ 60g potassium hydroxide or sodium hydroxide and 100 ~ 300mg Sodium Glutamate;
(2) insert in described electroplate liquid with the base material of electroplated and pass into electric current, apply ultrasonic wave simultaneously and electroplate.
Wherein, described electric current is monopulse rectangular wave current; The pulsewidth of described monopulse rectangular wave current is 0.5 ~ 1ms, and dutycycle is 5 ~ 30%, and average current density is 0.5 ~ 3A/dm
2.
Wherein, in described step (2), the pH of electroplate liquid is 11 ~ 13.
Wherein, in described step (2), the temperature of electroplate liquid is 70 ~ 80 DEG C.
Wherein, in described step (2), the time of plating is 20 ~ 40min.
Wherein, in described step (2), the anode of plating and the area ratio of negative electrode are (1 ~ 4): 1.
Wherein, in described step (2), described base material is nickel, titanium, tantalum, copper or silver.
Carry out under being plated on Ultrasonic Conditions in the present invention.Hyperacoustic applying mode can adopt ultrasonic generator.The present invention without particular requirement, can adopt commercially available to the concrete model of ultrasonic generator and structure.The hyperacoustic actual conditions of ultrasonic generator, such as ultrasonic power, frequency etc., also have no special requirements, and specifically can select according to practical situation.
Monopulse rectangular wave current is defined as at t
1passing into current density in time is J
pelectric current, at t
2without passing into electric current in time, it is a kind of intermittent pulse current.Dutycycle is defined as t
1/ (t
1+ t
2), frequency is 1/ (t
1+ t
2), mean current is defined as J
pt
1/ (t
1+ t
2).Compare with DC electrodeposition, thickness and the ion concentration distribution of electrostatic double layer all change; While adding electrochemical polarization, reduce concentration polarization, the direct effect of generation is, the coating that pulse plating obtains than DC electrodeposition coating evenly, crystallization is finer and closely woven.Moreover, pulse plating also has: hardness and the wear resistance of (1) coating are all high; (2) solution dispersibility and covering power good; (3) decrease the super plating of part edge, coating distributing homogeneity is good, can save plating solution usage quantity.
The present invention does not add restriction to the process of plating piece after the treatment process of the base material of electroplated before plating and plating, can take conventional pretreatment process, such as cleaning before copper plating, polishing etc.The selection of the electrode of plating also can adopt conventional method to carry out.
The present invention for the main salt of platinum, is brightening agent with Sodium Glutamate with hexahydroxy-potassium platinate, and add potassium hydroxide or sodium hydroxide plating solution for alkalescence, make the plating solution of acquisition have good dispersion force and covering power thus, cathode efficiency is high, and plating solution performance is excellent.The porosity that employing electroplates the coating of acquisition in the basic conditions at plating solution is low, and luminance brightness is high, and quality of coating is good.
Embodiment
Technical scheme of the present invention is further illustrated below in conjunction with embodiment.
Embodiment 1
The formula of electroplate liquid is as follows:
Plating technology condition: the pulsewidth of monopulse rectangular wave current is 0.5ms, and dutycycle is 30%, and average current density is 0.5A/dm
2; PH is 11, and temperature is 70 DEG C, and electroplating time is 40min.
Embodiment 2
The formula of electroplate liquid is as follows:
Plating technology condition: the pulsewidth of monopulse rectangular wave current is 0.6ms, and dutycycle is 25%, and average current density is 0.8A/dm
2; PH is 13, and temperature is 80 DEG C, and electroplating time is 35min.
Embodiment 3
The formula of electroplate liquid is as follows:
Plating technology condition: the pulsewidth of monopulse rectangular wave current is 0.8ms, and dutycycle is 20%, and average current density is 3A/dm
2; PH is 12, and temperature is 70 DEG C, and electroplating time is 20min.
Embodiment 4
The formula of electroplate liquid is as follows:
Plating technology condition: the pulsewidth of monopulse rectangular wave current is 1ms, and dutycycle is 15%, and average current density is 2.5A/dm
2; PH is 11.5, and temperature is 75 DEG C, and electroplating time is 25min.
Embodiment 5
The formula of electroplate liquid is as follows:
Plating technology condition: the pulsewidth of monopulse rectangular wave current is 0.9ms, and dutycycle is 5%, and average current density is 2A/dm
2; PH is 12.5, and temperature is 75 DEG C, and electroplating time is 30min.
Embodiment 6
The formula of electroplate liquid is as follows:
Plating technology condition: the pulsewidth of monopulse rectangular wave current is 0.7ms, and dutycycle is 10%, and average current density is 1.5A/dm
2; PH is 12, and temperature is 75 DEG C, and electroplating time is 35min.
With reference to following methods, dispersive ability test is carried out to the plating solution of embodiment 1 ~ 6:
The dispersive ability of plating solution adopts far and near cathode method (Haring-Blue method) to measure.Measure the Hull groove that groove adopts the HullCell267ml model of Kocour company of the U.S., interior dimensions is 150mm × 50mm × 70mm.Negative electrode selects thickness to be the copper sheet of 0.5mm, and working face is of a size of 50mm × 50mm; Anode is plating nickel plate with holes; Plating electric current 1A, electroplating time 30min.
The dispersive ability calculation formula of plating solution is:
Dispersive ability=[K-(the Δ M of plating solution
1/ Δ M
2)]/(K-1) (result represents with percentage);
In formula, K is negative electrode far away to the distance of anode and nearly negative electrode to the ratio of distances constant of anode, and in this test, K gets 2; Δ M
1for the increment (g) after plating on nearly negative electrode; Δ M
2for the increment (g) after plating on negative electrode far away.
With reference to following methods, covering power test is carried out to the plating solution of embodiment 1 ~ 6:
Endoporus method is adopted to measure.Negative electrode selects internal diameter l10mm, and pipe range is the copper pipe of 50mm, and one end is closed.During test, the distance of the mouth of pipe and anode is fixed on 80mm, test current 0.2A, electroplating time 30min.According to following formulae discovery:
Covering power=endoporus coating length/pipe range (result represents with percentage).
With reference to following methods, current efficiency test is carried out to the plating solution of embodiment 1 ~ 6:
Copper voltameter method is adopted to measure.Negative electrode to be tested and copper voltameter cleaned and dry up rear electronic scale weighing, then insert in electrodeposit groove by two negative electrodes simultaneously, be energized 10 ~ 30min, take out and clean dry up after use electronic scale weighing.According to following formulae discovery:
Current efficiency=(1.186 × cathode quality to be measured)/(electrochemical equivalent of copper voltameter quality × cathodic deposition metal to be measured) × 100%.Here, electrochemical equivalent=molar mass ÷ (depositing ions valency × 26.8), unit is g.A
-1.h
-1.In this test, tetravalence Pt electrochemical equivalent is 1.820g.A
-1.h
-1.
Speed test is plated with reference to the plating solution of following methods to embodiment 1 ~ 6:
Mass method is adopted to measure sedimentation rate.Be 10 with sensitivity
-4electronic balance weighing sample plating before and after quality.By the acquisition sedimentation rate of poor quality of unit time, unit surface, press formulae discovery below:
Plating speed=(after plating before sample mass-plating sample mass)/(specimen surface to be plated long-pending × plating time).Each Data duplication is measured three times and is got its mean value.
Test with reference to the bonding force of following methods to the coating of embodiment 1 ~ 6:
The method adopting line to draw lattice measures the bonding force of coating, is specially: being 30 degree with one cutting edge by electrodeposition cladding, converted steel draws parallel lines or the 1mm that 2mm of being separated by drawn by cutter
2square lattice.Whether the coating observing line tilts or peels off.Should master the dynamics during line, a cutter just can scratch coating, arrives matrix metal.Adopt quench to measure the bonding force of coating, be specially: the test piece of having plated is placed in retort furnace quenching in the cold water being heated to 300 DEG C of insulation 30min taking-up immersion 10 DEG C immediately, observe coating and whether occur bubble and decortication phenomenon.
With reference to following methods, toughness test is carried out to the coating of embodiment 1 ~ 6:
Coating is stripped down, is bent to 180 °, and extrudes knee, observe coating and whether occur fracture.
With reference to following methods, porosity test is carried out to the coating of embodiment 1 ~ 6:
The large young pathbreaker of porosity is directly connected to the corrosion resisting property of coating, adopts paster method to press GB5935-86 standard detection.The etchant solution that the potassium ferricyanide solution of 10g/L and the sodium chloride solution of 20g/L are tested as porosity.Operation steps is: after wiped clean of being deoiled by coating surface, is close to coating surface with the filter paper soaking into etchant solution, and the two can not have gap.Buy the fully wetting filter paper of etchant solution solution by glass stick or degreasing swab stick, supplement a solution at interval of 1min, taken off by filter paper after 5min, dry after clean with distilled water flushing, record hole is counted.Be placed on cleaned glass plate and dry, the number of number Bluepoint.Substitute into formulae discovery voidage below:
Number/tested area (individual/the cm of porosity=spot
2);
When calculating number of apertures, do following calculating by spot diameter size: hot spot diameter is less than 1mm, and with a porosimeter at often; Be greater than 1mm and be less than 3mm often o'clock with three porosimeters; Be greater than 3mm and be less than 5mm, often with ten porosimeters.
With reference to following methods, Surface flat test is carried out to the coating of embodiment 1 ~ 6:
By the Hull groove of the HullCell267ml model with the Kocour company of the test piece U.S. after 200 order sand paperings evenly at 3A/dm
2dC current density carries out plating 10min at 25 DEG C of temperature, and whether then observe test piece has scratch.
To expose aptitude tests with reference to the coating of following methods to embodiment 1 ~ 6:
Adopt the Hull groove of the HullCell267ml model of Kocour company of the U.S. at 3A/dm
2after DC current density carries out plating 10min at 25 DEG C of temperature, observe the surface luminous intensity of coating.
The test result of the coating of embodiment 1 ~ 6 and comparative example and the performance of plating solution is as follows:
As can be seen from the above table, in embodiment 1 ~ 6, consider from the integration test effect of plating solution and coating, the dispersive ability of the formula plating solution of embodiment 6, covering power, current efficiency and plating speed, the porosity of coating and bonding force will be got well compared with other embodiment.Thus, this formula is screening formulation of the present invention, and the preferred plating conditions of its correspondence is the pulsewidth of monopulse rectangular wave current is 0.7ms, and dutycycle is 10%, and average current density is 1.5A/dm
2; PH is 12, and temperature is 75 DEG C, and electroplating time is 35min, and male and femal face is long-pending than being 3:1.
It should be noted that and understand, when not departing from the spirit and scope of accompanying claim the present invention for required protection, various amendment and improvement can be made to the present invention of foregoing detailed description.Therefore, the scope of claimed technical scheme is not by the restriction of given any specific exemplary teachings.
Below know-why of the present invention is described in conjunction with specific embodiments.These describe just in order to explain principle of the present invention, and can not be interpreted as limiting the scope of the invention by any way.Based on explanation herein, those skilled in the art does not need to pay performing creative labour can associate other embodiment of the present invention, and these modes all will fall within protection scope of the present invention.
Claims (9)
1. an alkali plating solution for electroplatinizing, is characterized in that, comprises in platinum 10 ~ 20g/L hexahydroxy-potassium platinate, 20 ~ 60g/L potassium hydroxide or sodium hydroxide and 100 ~ 300mg/L Sodium Glutamate.
2. plating solution according to claim 1, is characterized in that, comprises in platinum 14g/L hexahydroxy-potassium platinate, 50g/L potassium hydroxide or sodium hydroxide and 180mg/L Sodium Glutamate.
3. an electric plating method, is characterized in that, comprises the following steps:
(1) electroplate liquid is prepared: in water, dissolve each feed composition form electroplate liquid, described often liter of electroplate liquid contains in platinum 10 ~ 20g hexahydroxy-potassium platinate, 20 ~ 60g potassium hydroxide or sodium hydroxide and 100 ~ 300mg Sodium Glutamate;
(2) insert in described electroplate liquid with the base material of electroplated and pass into electric current, apply ultrasonic wave simultaneously and electroplate.
4. want the method described in 4 according to right, it is characterized in that, described electric current is monopulse rectangular wave current; The pulsewidth of described monopulse rectangular wave current is 0.5 ~ 1ms, and dutycycle is 5 ~ 30%, and average current density is 0.5 ~ 3A/dm
2.
5. method according to claim 4, is characterized in that, in described step (2), the pH of electroplate liquid is 11 ~ 13.
6. method according to claim 4, is characterized in that, in described step (2), the temperature of electroplate liquid is 70 ~ 80 DEG C.
7. method according to claim 4, is characterized in that, in described step (2), the time of plating is 20 ~ 40min.
8. method according to claim 4, is characterized in that, in described step (2), the anode of plating and the area ratio of negative electrode are (1 ~ 4): 1.
9. method according to claim 4, is characterized in that, in described step (2), described base material is nickel, titanium, tantalum, copper or silver.
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201510604424.3A CN105132965A (en) | 2015-09-21 | 2015-09-21 | Alkaline plating solution for platinum electroplating and electroplating method adopting alkaline plating solution |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201510604424.3A CN105132965A (en) | 2015-09-21 | 2015-09-21 | Alkaline plating solution for platinum electroplating and electroplating method adopting alkaline plating solution |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106391139A (en) * | 2016-09-09 | 2017-02-15 | 昆明理工大学 | Method for preparing hexahydroxyplatinate bi-(ethanol amine) water solution by electrodialysis process |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5310475A (en) * | 1990-06-29 | 1994-05-10 | Electroplating Engineers Of Japan, Limited | Platinum electroforming and platinum electroplating |
| CN1534110A (en) * | 2003-03-31 | 2004-10-06 | 田中贵金属工业株式会社 | Sputtering target material |
-
2015
- 2015-09-21 CN CN201510604424.3A patent/CN105132965A/en active Pending
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5310475A (en) * | 1990-06-29 | 1994-05-10 | Electroplating Engineers Of Japan, Limited | Platinum electroforming and platinum electroplating |
| CN1534110A (en) * | 2003-03-31 | 2004-10-06 | 田中贵金属工业株式会社 | Sputtering target material |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106391139A (en) * | 2016-09-09 | 2017-02-15 | 昆明理工大学 | Method for preparing hexahydroxyplatinate bi-(ethanol amine) water solution by electrodialysis process |
| CN106391139B (en) * | 2016-09-09 | 2019-06-11 | 昆明理工大学 | A kind of method that electroosmose process prepares hexahydroxy platinic acid two (ethanol amine) aqueous solution |
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Application publication date: 20151209 |