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CN1032040A - The method for preparing composite tin-plating layer - Google Patents

The method for preparing composite tin-plating layer Download PDF

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Publication number
CN1032040A
CN1032040A CN 88106559 CN88106559A CN1032040A CN 1032040 A CN1032040 A CN 1032040A CN 88106559 CN88106559 CN 88106559 CN 88106559 A CN88106559 A CN 88106559A CN 1032040 A CN1032040 A CN 1032040A
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China
Prior art keywords
plating layer
preparing composite
grams per
composite tin
ceramic
Prior art date
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Withdrawn
Application number
CN 88106559
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Chinese (zh)
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CN1008749B (en
Inventor
唐致远
郭鹤桐
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Tianjin University
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Tianjin University
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Publication date
Application filed by Tianjin University filed Critical Tianjin University
Priority to CN 88106559 priority Critical patent/CN1008749B/en
Publication of CN1032040A publication Critical patent/CN1032040A/en
Publication of CN1008749B publication Critical patent/CN1008749B/en
Expired legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D15/00Electrolytic or electrophoretic production of coatings containing embedded materials, e.g. particles, whiskers, wires
    • C25D15/02Combined electrolytic and electrophoretic processes with charged materials

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Electroplating And Plating Baths Therefor (AREA)

Abstract

A kind of method for preparing composite tin-plating layer, the plating bath that it uses is made up of following ingredients: stannous sulfate 30-70 grams per liters, sulfuric acid 80-160 grams per liters, 15 milliliters/liter of SS-820 (joining the cylinder brightening agent), 1.5 milliliters/liter of SS-821 (interpolation brightening agent), metal ceramic powder 0.2-5.5 grams per liters.The tin coating that adopts this plating bath to plate out has good brazing property, is suitable for the production of electronic devices and components.

Description

The method for preparing composite tin-plating layer
The invention relates to electric plating method, more particularly, is the method about acid bright tinning.
In recent years, along with developing rapidly of electronic industry, in order to improve the weldability of electronic devices and components, and the metals such as gold and silver of conserve expensive, people attempt to plate the good tin of solderability on the lead-in wire of electronic devices and components." electroplating and environmental protection " " acid bright tinning novel process " literary composition on magazine the 2nd phase of nineteen eighty-two that China publishes discloses a kind of method of acid bright tinning, and the prescription of the electroplate liquid that this method adopts is:
Stannous sulfate 70 grams per liters
Sulfuric acid 160 grams per liters
SS-820(joins the cylinder brightening agent) 15 milliliters/liter
SS-821(adds brightening agent) 1.5 milliliters/liter
Use the plating bath of this prescription to electroplate, can obtain the coating of light on the lead-in wire of electronic devices and components, weak point is that the brazing property instability of coating is through coating blackening afterwards in, two month, solderability variation.
The objective of the invention is to overcome above-mentioned shortcoming, make coating have good brazing property, and good stability, can keep light and good solderability in a long time.
The method that the present invention prepares composite tin-plating layer is to use the electroplate liquid of following component:
Stannous sulfate 30-70 grams per liter
Sulfuric acid 80-160 grams per liter
SS-820(joins the cylinder brightening agent) 15 milliliters/liter
SS-821(adds brightening agent) 1.5 milliliters/liter
Add additive sintering metal micro mist 0.2-5.5 grams per liter in above-mentioned plating bath, the diameter of described ceramic micropowder particle is less than 5 microns.
Above-mentioned ceramic can be any among aluminum oxide, the boron nitride, also can be the mixture of aluminum oxide and boron nitride, certainly, also can be other ceramic, for example plumbous oxide, silicon carbide etc.Wherein the add-on of aluminum oxide and boron nitride was advisable with 2: 1.
Ceramic carries out the appropriate location reason before adding plating bath, effect is better.Its treatment step is: (a) with ceramic in 1: the ratio of 2-5 adds distilled water, is placed in the ball mill to grind 4-8 hour; (b) above-mentioned micro mist liquid slurry is put into the sulfuric acid that concentration is 1-5M, be heated to 80-100 ℃, be incubated 1-3 hour, and constantly stir; (c) the cooling said mixture filters then, and cleans with distilled water, until the pH value of aqueous cleaning solution till the 6-7; (d) above-mentioned ceramic is put into plating bath, and stir, make it even.
Characteristics of the present invention are to add ceramic in the electroplate liquid of existing technology, for example aluminum oxide and boron nitride.This way and tradition are electroplated theoretical running in the opposite direction, yet practice shows, not only light, solidity to corrosion are good to adopt the coating that electroplate liquid plated out that is mixed with ceramic, and brazing property is good, and this is unhoped-for.
Below by embodiment, can do further understanding to the present invention.Wherein example 1 is a prior art, and remaining example is a content of the present invention.
Example 1
Prescription is as follows with technology:
Stannous sulfate (analytical pure) 40 grams per liters
Sulfuric acid (analytical pure) 100 grams per liters
SS-820(joins the cylinder brightening agent) 15 milliliters/liter
SS-821(adds brightening agent) 1.5 milliliters/liter
The temperature room temperature
30 minutes time
4 amperes/decimeter of current densities 2
30 rev/mins of rotating speeds
Anode and cathode area were than 2: 1
Example 2
Add analytically pure ceramic (particle diameter is less than 5 microns) aluminum oxide 1 grams per liter and boron nitride 2 grams per liters in the plating bath of example 1, other processing condition are identical with example 1.
Example 3
Add analytically pure ceramic (particle diameter is less than 5 microns) aluminum oxide 5 grams per liters and boron nitride 0.5 grams per liter in the plating bath of example 1, other processing condition are identical with example 1.
Example 4
Add analytically pure ceramic (particle diameter is less than 5 microns) aluminum oxide 0.1 grams per liter and boron nitride 0.1 grams per liter in the plating bath of example 1, other processing condition are identical with example 1.
Example 5
Add analytically pure ceramic (particle diameter is less than 5 microns) aluminum oxide 1 grams per liter and boron nitride 0.5 grams per liter in the plating bath of example 1, other processing condition are identical with example 1.
The salient features of the tin coating that the various embodiments described above plate out (lead-in wire with 0.5 millimeter of diameter is an example) is shown in the table.As can be seen from the table, adopt the tin coating of method preparation of the present invention that following advantage is compared with prior art arranged: the brazing property of coating (wetting power) is good, zero friendship time is short, coating hardness is high, porosity is low.In addition, the coating luminance brightness is good, stability strong, and coating is deposited after half a year still very bright in air, and considerable change does not take place its good weldability.
Figure 881065595_IMG1

Claims (6)

1, a kind of method for preparing composite tin-plating layer, use the plating bath of following component: stannous sulfate 30-70 grams per liter, sulfuric acid 80-160 grams per liter, 15 milliliters/liter of SS-820 (joining the cylinder brightening agent), 1.5 milliliters/liter of SS-821 (interpolation brightening agent), it is characterized in that, add additive sintering metal micro mist 0.2-5.5 grams per liter in above-mentioned plating bath, the diameter of described ceramic micropowder particle is less than 5 microns.
2, the method for preparing composite tin-plating layer according to claim 1 is characterized in that, described ceramic is an aluminum oxide.
3, the method for preparing composite tin-plating layer according to claim 1 is characterized in that, described ceramic is a boron nitride.
4, the method for preparing composite tin-plating layer according to claim 1 is characterized in that, described ceramic is the mixture of aluminum oxide and boron nitride.
5, the method for preparing composite tin-plating layer according to claim 4 is characterized in that, described aluminum oxide is 2: 1 with the ratio of boron nitride.
According to the described method for preparing composite tin-plating layer of claim 1 to 5, it is characterized in that 6, described ceramic is adding the following processing of plating bath previous crops: (a) with ceramic in 1: the ratio of 2-5 adds distilled water, is placed in the ball mill grinding 4-8 hour; (b) above-mentioned micro mist liquid slurry is put into the sulfuric acid that concentration is 1-5M, be heated to 80-100 ℃, be incubated 1-3 hour, and constantly stir; (c) the cooling said mixture filters then, and cleans with distilled water, until the pH value of aqueous cleaning solution till the 6-7; (d) above-mentioned ceramic is put into plating bath and stir, make it even.
CN 88106559 1988-09-28 1988-09-28 Process for preparation of composite tin-plating layer Expired CN1008749B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 88106559 CN1008749B (en) 1988-09-28 1988-09-28 Process for preparation of composite tin-plating layer

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 88106559 CN1008749B (en) 1988-09-28 1988-09-28 Process for preparation of composite tin-plating layer

Publications (2)

Publication Number Publication Date
CN1032040A true CN1032040A (en) 1989-03-29
CN1008749B CN1008749B (en) 1990-07-11

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ID=4834284

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 88106559 Expired CN1008749B (en) 1988-09-28 1988-09-28 Process for preparation of composite tin-plating layer

Country Status (1)

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CN (1) CN1008749B (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101041903A (en) * 2006-03-24 2007-09-26 富士通株式会社 Plating film and forming method thereof
CN103215622A (en) * 2012-06-13 2013-07-24 安徽恒晶电缆集团有限公司 Method for electrotinning copper conductor of wire or cable
CN109735890A (en) * 2018-12-27 2019-05-10 大连理工大学 Nano TiO (titanium dioxide)2Preparation method of (E) -Sn micro bump
CN110438539A (en) * 2019-09-24 2019-11-12 郎溪蓉承金属表面处理有限公司 Electroplating technology with corrosion-resistant and conductivity kirsite substrate
CN110616451A (en) * 2019-06-21 2019-12-27 西南交通大学 Method for enhancing strength of welding interface of hard alloy and metal

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101041903A (en) * 2006-03-24 2007-09-26 富士通株式会社 Plating film and forming method thereof
US20100170804A1 (en) * 2006-03-24 2010-07-08 Fujitsu Limited Plating film and forming method thereof
CN103215622A (en) * 2012-06-13 2013-07-24 安徽恒晶电缆集团有限公司 Method for electrotinning copper conductor of wire or cable
CN109735890A (en) * 2018-12-27 2019-05-10 大连理工大学 Nano TiO (titanium dioxide)2Preparation method of (E) -Sn micro bump
CN109735890B (en) * 2018-12-27 2020-10-13 大连理工大学 Nano TiO (titanium dioxide)2Preparation method of (E) -Sn micro bump
CN110616451A (en) * 2019-06-21 2019-12-27 西南交通大学 Method for enhancing strength of welding interface of hard alloy and metal
CN110438539A (en) * 2019-09-24 2019-11-12 郎溪蓉承金属表面处理有限公司 Electroplating technology with corrosion-resistant and conductivity kirsite substrate

Also Published As

Publication number Publication date
CN1008749B (en) 1990-07-11

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