CN103882484B - High-speed tin plating plating solution - Google Patents

High-speed tin plating plating solution Download PDF

Info

Publication number
CN103882484B
CN103882484B CN201410135617.4A CN201410135617A CN103882484B CN 103882484 B CN103882484 B CN 103882484B CN 201410135617 A CN201410135617 A CN 201410135617A CN 103882484 B CN103882484 B CN 103882484B
Authority
CN
China
Prior art keywords
plating solution
plating
tin
agent
acid
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.)
Expired - Fee Related
Application number
CN201410135617.4A
Other languages
Chinese (zh)
Other versions
CN103882484A (en
Inventor
黎德育
王志登
王熙禹
王洺浩
李宁
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Harbin Institute of Technology
Original Assignee
Harbin Institute of Technology
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Harbin Institute of Technology filed Critical Harbin Institute of Technology
Priority to CN201410135617.4A priority Critical patent/CN103882484B/en
Publication of CN103882484A publication Critical patent/CN103882484A/en
Application granted granted Critical
Publication of CN103882484B publication Critical patent/CN103882484B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Abstract

The invention discloses a kind of high-speed tin plating plating solution, described plating solution includes following composition: 5-100g/L tin methane sulfonate, 10-100mL/L pyrovinic acid, 0.1-20ml/L sulphuric acid, 0.1-200mg/L defoamer, 0.1-50g/L carefully brilliant agent, 0.01-20g/L walk agent, 0.1-40g/L antioxidant.The plating solution dispersion of the present invention and covering power are excellent, it is possible to meet every technology requirement of high speed tin plating production line, can reduce tin coating weight (≈ 0.7g/m further simultaneously2) to economize on resources, plating solution iron ion and chloride ion tolerance limit content best result be not up to 20g/L, 1000ppm in addition.The plating solution that the present invention obtains is than the bath stability of non-refinement crystalline substance agent, and plating solution uses, placement still can obtain good coating after several weeks.

Description

High-speed tin plating plating solution
Technical field
The invention belongs to the technical field of electrochemical deposition of metal and alloy, relate to a kind of high-speed tin plating plating solution.
Background technology
High-speed tin plating is widely used in sheet material, wire rod and electronics finishing, for electrolytic tinplate (being commonly called as tinplate), it is a kind of functional material, have that intensity height, weldability be good, corrosion-resistant and the feature such as avirulence, the long-term main packaging material as food industry, and it is widely used in medicine, light industry, automobile and other industries, it is one of most popular steel product.
The smooth electroplating technology of fluorine Loews that existing electrotinning technique adopts phenolsulfonic acid (PSA) to be master mostly, the plating line of this technique accounts for the 65.7% of world's electrotinned wire, but containing the phenolic compound that toxicity is very big in PSA, and the treatment cost of waste liquor produced is also higher.This plating solution limiting current density is low, so that domestic unit actual motion speed is about 175m/min (unit design linear velocity is generally ~ 600m/min), production efficiency also has the very big rising space.Additive and plating solution performance thereof are required height by high-speed tin plating, and plated material to overcome parallel electric field, gas field, temperature field, flow field and concentration field effect, obtain high-quality coating in 10s.Additionally, domestic tin plating unit adopts block tin as soluble anode greatly, need to regularly shutting down replacing anode, production efficiency is low, and stannum mud volume production goes out many, and labor strength is big;The insoluble anode such as iridium dioxide and platinum plating is following application tendency.In production process, insoluble anode precipitates out active oxygen in a large number, and some tin plating additives are very easily aging.Therefore the additive of high speed tin plating and plating solution thereof are just seemed particularly urgent.
CN101922026A discloses a kind of pyrovinic acid system Asia matte pure tin electroplating additive and plating solution thereof, its additive contains the disagreeableness heterocycle compound of environment and aminated compounds, in addition this plating solution is possibly together with the organic solvent of 100-150g/L, in high-speed motion strong convection, organic solvent volatilizees rapidly, stannum mud amount controls not good, plating solution very easily lost efficacy, and improved production cost, also to workshop environment.CN1570219 discloses electroplating composition and electro-plating method, and its compositions contains thiourea and aminated compounds, and decomposes releases nitrogen, sulfur oxide, is unfavorable for that operator's is healthy.CN1733977A discloses a kind of tin plating additive and preparation method thereof, and its additive contains polyoxyethylene aniline ether, LOMAR PWA EINECS 246-676-2 etc. to the disagreeableness chemical substance of environment.
US7517443B2 discloses a kind of electrotinning plating solution, is mainly composed of the additive of sulfamic acid stannum, sulphuric acid and the oxirane containing N and propylene oxide block copolymer;Consider conduct hydrolysis and the stable required strong acid condition of stannous ion of sulfamic acid, also need further checking for high-speed tin plating.USRE39476E discloses a kind of tin bath solution composition, wherein contains polyoxyalkylene alcohol homopolymer and oxirane and epoxy propane copolymer composition, and plating solution also needs to optimize in foaming and defoaming capacity;In this patent, antioxidant only has one or more of catechol, resorcinol and hydroquinone simultaneously, it is impossible to effectively suppress the grey black that soft-melting process brings to tin-plated product.
Summary of the invention
Offer one is provided and can be used for high-speed tin plating plating solution, be intended, primarily, to improve plating solution performance, improve quality of coating, and meet high speed electrodeposition requirement;And optimize High Speed Tin Plating Technology by this approach, reduce original product consumption, reduce production cost, and realize the production domesticization of high-speed tin plating additive and plating solution thereof simultaneously.
It is an object of the invention to be achieved through the following technical solutions:
A kind of for high-speed tin plating plating solution, including following composition: tin methane sulfonate 5-100g/L, pyrovinic acid 10-100mL/L, sulphuric acid 0.1-20ml/L, additive: 0.1-200mg/L defoamer, 10-50g/L carefully brilliant agent, 0.01-20g/L walk agent, 0.1-40g/L antioxidant.
In the present invention, described defoamer is a compounds of polyoxyethylene oxypropylene glycerol, and molecular weight is at 500-15000.
In the present invention, described one or more the mixture that thin brilliant agent is formaldehyde, oxirane and epoxy propane copolymer.It is preferably the block copolymer of formaldehyde, oxirane and expoxy propane and the mixture of random copolymer one, two or three arbitrary proportion.
In the present invention, described thin brilliant agent block polymer is MOx-EOy、POx-EOy、MOx-EOy-MOz、EOx-MOy-EOz、MOx-EOy-POz、EOx-MOy-POz、EOx-POy-MOz、POx-EOy-POz、EOx-POy-EOzAnd random copolymer is MOmEOnPOt.Wherein, MO to be methoxyl group, EO be ethyoxyl, PO are propoxyl group;X, y, z is the degree of polymerization of MO, EO, PO of block copolymer, x, y, z, m, n and t range for 1-60.
In the present invention, described thin brilliant agent EO mass content is at 5-90%, and polymer molecular weight is between 2000-10000, and density is at 1.10 ± 0.10g/cm3, cloud point is at 55-95 DEG C.
In the present invention, the described agent that walks is for a kind of alkyl alcohol ethoxylates, it is possible to increase plating solution limiting current density value.Its structural formula is R-O-(CH2CH2O) n-H, R are the branched hydrocarbyl of saturated C7 ~ 13, and n is within 60-280.
In the present invention, described antioxidant is any two kinds in hydroquinone, catechol, resorcinol, ascorbic acid, malic acid, citric acid, tartaric acid, with 1:0.1-5 mixed in molar ratio.
The present invention, compared to prior art, has a characteristic that
1, high-speed tin plating additive provided by the invention is without anions and canons and amphoteric surfactant, polyformaldehyde and poly(ethylene oxide) and the homopolymer of poly(propylene oxide), aldehydes, heterocycle compound, aminated compounds, polyaminocarboxylic acid, sulfur aminoacid and any organic solvent.
2, the present invention configures water used by additive concentrating liquid and plating solution is deionized water, electrical conductivity < 20 μ S/cm;Gained coating is canescence Asia light coating.
3, the plating solution operating temperature of additive of the present invention composition is interval at 10-70 DEG C;Under high-speed condition, the plating solution limiting current density containing additive of the present invention can reach 60-120A/dm2
4, additive of the present invention forms plating solution dispersion and covering power are excellent, it is possible to meet every technology requirement of high speed tin plating production line, can reduce tin coating weight (≈ 0.7g/m further simultaneously2) to economize on resources, plating solution iron ion and chloride ion tolerance limit content best result be not up to 20g/L, 1000ppm in addition.
5, when the plating solution energy on-line velocity of additive of the present invention composition is 0-800m/min, it is thus achieved that crystallization is careful, covers uniform coating.
6, the additive of the present invention and the plating solution of composition thereof do not contain nonbiodegradable substance and to the disagreeableness chemicals of environment, and sewage disposal is simple, meets environmental requirement, is worth promoting the use of in high speed tin plating industry.
7, the plating solution that the present invention obtains is than the bath stability of non-refinement crystalline substance agent, and plating solution uses, placement still can obtain good coating after several weeks.
Accompanying drawing explanation
Fig. 1 is embodiment 1 Hull cell sample photo, and experiment condition is 45 DEG C, 2A, and 2min, without convection agitation;
Fig. 2 is embodiment 2 Hull cell sample photo, and experiment condition is 45 DEG C, 2A, and 2min, without convection agitation;
Fig. 3 is embodiment 3 Hull cell sample photo, and experiment condition is 45 DEG C, 2A, and 2min, without convection agitation;
Fig. 4 is that embodiment 1 is at 15.0A/dm2The 0.7g/m obtained under different current density condition2Tin plate SEM photograph;
Fig. 5 is that embodiment 1 is at 15.0A/dm2The 0.7g/m obtained2Coating tin plate SEM photograph local energy spectrum analysis (spectrogram 2);
Fig. 6 is that embodiment 1 is at 15.0A/dm2The 0.7g/m obtained2Coating tin plate SEM photograph local energy spectrum analysis (spectrogram 3);
Fig. 7 is that embodiment 1 is at 6.75A/dm2The 1.1g/m obtained under condition2Tin plate SEM photograph;
Fig. 8 is that embodiment 1 is at 15.0A/dm2The 1.1g/m obtained under condition2Tin plate SEM photograph;
Fig. 9 is that embodiment 1 is at 24.75A/dm2The 1.1g/m obtained under condition2Tin plate SEM photograph;
Figure 10 is that embodiment 1 is at 15.0A/dm2The 1.1g/m obtained2Coating tin plate SEM photograph local energy spectrum analysis (spectrogram 3);
Figure 11 is that embodiment 1 is at 15.0A/dm2The 1.1g/m obtained2Coating tin plate SEM photograph local energy spectrum analysis (spectrogram 4);
Figure 12 is that embodiment 1 is at 15.0A/dm2The 1.1g/m obtained under condition26000 times of SEM photograph of tin plate;
Figure 13 is that embodiment 2 is at 15.0A/dm2The 1.1g/m obtained under condition26000 times of SEM photograph of tin plate;
Figure 14 is that embodiment 3 is at 15.0A/dm2The 1.1g/m obtained under condition26000 times of SEM photograph of tin plate.
Detailed description of the invention
Below in conjunction with embodiment, technical scheme being further described, plating solution composition and process conditions can be adjusted according to product demand.Every technical solution of the present invention modified or equivalent replaces, without deviating from the spirit and scope of technical solution of the present invention, all should be encompassed in protection scope of the present invention.
Embodiment 1
Tin methane sulfonate 45g/L
Methanesulfonic acid 45ml/L
Sulphuric acid 10ml/L
Polyoxyethylene oxypropylene glycerol (molecular weight 4000) 0.1mg/L
MO15-EO21-PO3010g/L
Capryl alcohol polyoxyethylene ether (molecular weight 8000) 0.6g/L
Hydroquinone+malic acid 15g/L
Temperature 45 C
Embodiment 2
Tin methane sulfonate 15g/L
Methanesulfonic acid 30ml/L
Sulphuric acid 10ml/L
Polyoxyethylene oxypropylene glycerol (molecular weight 8000) 0.1mg/L
PO10-EO42-PO1030g/L
Capryl alcohol polyoxyethylene ether (molecular weight 2000) 0.01g/L
Hydroquinone+malic acid 10g/L
Temperature 25 DEG C
Embodiment 3
Tin methane sulfonate 75g/L
Methanesulfonic acid 100ml/L
Sulphuric acid 15ml/L
Polyoxyethylene oxypropylene glycerol (molecular weight 12000) 0.1mg/L
EO30-PO3015g/L
Capryl alcohol polyoxyethylene ether (molecular weight 8000) 15g/L
Hydroquinone+tartaric acid 20g/L
Temperature 45 C
Plating solution performance is tested
1) Hull groove test piece test.Testing with 267mL plating solution, test piece adopts the long 100mm of cold-rolled steel sheet, is highly 70mm.Experiment condition is 45 DEG C, 2A, and 2min, without convection agitation.After sample plating, taking-up deionized water is cleaned and is dried up, and measures coating scorch region width, and embodiment 1,2,3 formula Hull test piece photo is referring to Fig. 1-3, and in a static condition, limiting current density is up to 8.5A/dm for this plating solution2, and occur without defective coating in whole electric current density district, it is possible to meet existing tin plating technique.
2) covering power test.Using endoporus method, test specimen adopts internal diameter to be 10mm, the long copper pipe for 50mm, uses pore to be facing perpendicularly to positive plate during plating, and the mouth of pipe is from anode 100mm, with 0.5A/dm2Cathode-current density plating 5min after pipe negative electrode is taken out, clean and dry up, cut vertically, measure pore coating and plate into the degree of depth, evaluate covering power.
Using the copper pipe that the plating solution that the additive of embodiment 1 formula is made into is plated to find after cutting open, copper pipe endoporus all goes up tin metal, illustrates that the plating solution covering power that the additive formulations that embodiment 1 provides is made into is good.
3) dispersibility test.Measure by far and near cathode method, coating bath transparent organic glass rectangular channel (inner chamber is of a size of 150mm × 50mm × 70mm), five sulculuses are opened uniformly for inserting negative electrode in the both sides of groove, negative electrode adopts thickness to be the cold-rolled steel sheet of 0.17mm, it is of a size of 5.5mm × 110mm, inactive face insulating tape seals, and uses the orificed anode with negative electrode same size, it is simple to plating solution flow of the electrolyte.Test current density is 1.0A/dm2, in the middle of two negative electrode test pieces, put into anode, remote negative electrode with and the distance ratio of nearly negative electrode and anode for 2:1, taking out negative electrode after electroplating 10min at 45 DEG C cleans up, and weighs the increment depositing metal on negative electrode remote, near, is calculated as follows the dispersibility of plating solution.
,
In formula: T dispersibility, %;
The distance ratio of the remote negative electrode of K and nearly negative electrode and anode;
The metal quality deposited on the nearly negative electrode of m1, g;
The metal quality deposited on the remote negative electrode of m2, g.
Additive 3 covering powers of test that embodiment 1 provides, data are table 1 such as:
TableParallel 3 the dispersibility test results of embodiment 1
Coating performance is tested
The cold-rolled steel sheet adopting temper rolling technology is object of study, and its surface does not only exist rolling lines, but also there is rolling pit, and high-speed tin plating additive and plating solution performance thereof are required high by this.Fig. 4-6 is that embodiment 1 is at 15.0A/dm2The 0.7g/m obtained under current density condition2Tin plate SEM photograph and SEM photograph local energy spectrum analysis data.Found that: plating solution is at 15.0A/dm2Under condition, 0.7g/m2Thin stannum amount tin plate sheet tin rolling direction and pit portion tin atom percentage ratio respectively 25.44%, 35.88%, the tin coating weight of pit is higher than rolling stricture of vagina place, and plating solution has certain leveling ability, is conducive to further thinning tin coating weight, saves tin resource.
Fig. 8-11 is the 1.1g/m that embodiment 1 obtains under different current density condition respectively2Tin plate SEM photograph and at 15.0A/dm2The 1.1g/m obtained2Coating tin plate SEM photograph local energy spectrum analysis data.Found that: under three kinds of current density condition, coating uniform and delicate, without dew plating, stannum crystal grain is careful.15.0A/dm2The 1.1g/m obtained under condition2Tin plate sheet tin rolling direction and pit portion tin atom percentage ratio respectively 62.25%, Sn62.17%, relatively 0.7g/m2Coating content has obvious rising, and pit and the tin atom percentage difference rolling lines place reduce further, and thickness is uniform.Therefore deducing that, the plating solution performance that embodiment 1 provides is excellent, and coating uniform and delicate is suitable to high speed electrodeposition process of tin.
Figure 12-14 is that embodiment 1,2,3 is at 15.0A/dm2The 1.1g/m obtained under condition26000 times of SEM photograph of tin plate;According to electromicroscopic photograph it can be seen that plated crystal tactical rule is uniform, zero defect.

Claims (6)

1. one kind is used for high-speed tin plating plating solution, it is characterized in that described plating solution includes following composition: 5-100g/L tin methane sulfonate, 10-100mL/L pyrovinic acid, 0.1-20ml/L sulphuric acid, 0.1-200mg/L defoamer, 10-50g/L carefully brilliant agent, 0.01-20g/L walk agent, 0.1-40g/L antioxidant, and described defoamer is polyoxyethylene oxypropylene glycerol;Described thin brilliant agent is MOx-EOy、POx-EOy、MOx-EOy-MOz、EOx-MOy-EOz、MOx-EOy-POz、EOx-MOy-POz、EOx-POy-MOzOr POx-EOy-POz, wherein MO to be methoxyl group, EO be ethyoxyl, PO are propoxyl group;X, y, z is the degree of polymerization of MO, EO, PO of block copolymer;X, y, z range for 1-60;The described agent that walks is alkyl alcohol ethoxylates.
2. according to claim 1 for high-speed tin plating plating solution, it is characterised in that the molecular weight of described polyoxyethylene oxypropylene glycerol is 500-15000.
3. according to claim 1 for high-speed tin plating plating solution, it is characterised in that described thin brilliant agent is MOmEOnPOtRandom copolymer, wherein MO to be methoxyl group, EO be ethyoxyl, PO are propoxyl group, and m, n, t are the unit number of MO, EO, PO of random copolymer, m, n and t range for 1-60.
4. according to claim 1 or 3 for high-speed tin plating plating solution, it is characterised in that described thin brilliant agent EO mass content is at 5-90%, and polymer molecular weight is between 2000-10000, and density is at 1.10 ± 0.10g/cm3, cloud point is at 55-95 DEG C.
5. according to claim 1 for high-speed tin plating plating solution, it is characterised in that described in the agent structural formula that walks be R-O-(CH2CH2O) n-H, R are the branched hydrocarbyl of saturated C7 ~ 13, and n is within 60-280.
6. according to claim 1 for high-speed tin plating plating solution, it is characterised in that described antioxidant is any two kinds in hydroquinone, catechol, resorcinol, ascorbic acid, malic acid, citric acid, tartaric acid.
CN201410135617.4A 2014-04-04 2014-04-04 High-speed tin plating plating solution Expired - Fee Related CN103882484B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201410135617.4A CN103882484B (en) 2014-04-04 2014-04-04 High-speed tin plating plating solution

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201410135617.4A CN103882484B (en) 2014-04-04 2014-04-04 High-speed tin plating plating solution

Publications (2)

Publication Number Publication Date
CN103882484A CN103882484A (en) 2014-06-25
CN103882484B true CN103882484B (en) 2016-06-29

Family

ID=50951593

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201410135617.4A Expired - Fee Related CN103882484B (en) 2014-04-04 2014-04-04 High-speed tin plating plating solution

Country Status (1)

Country Link
CN (1) CN103882484B (en)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104060308B (en) * 2014-06-30 2016-09-14 句容市博远电子有限公司 A kind of Pure Tin Plating Process liquid reducing dew copper phenomenon and application thereof
CN104988544A (en) * 2015-06-26 2015-10-21 吕小方 Electrolytic tinning annexing agent
CN105609729B (en) * 2015-12-30 2018-02-13 湖南永盛新材料股份有限公司 A kind of aluminium/copper/CNTs tin/graphite sandwich construction lithium ion battery negative material and preparation method thereof
CN105755512B (en) * 2016-03-04 2018-01-05 昆山艾森半导体材料有限公司 A kind of tin methane sulfonate antioxidant and preparation method thereof and application method
CN107502927B (en) * 2017-07-24 2019-07-02 奎克化学(中国)有限公司 A kind of methanesulfonate tin deposit solution
CN109267024B (en) * 2018-11-02 2020-11-20 常德力元新材料有限责任公司 Preparation method of foam tin material
CN110512241B (en) * 2019-09-29 2021-05-14 粤海中粤浦项(秦皇岛)马口铁工业有限公司 Electrotinning solution with good deep plating capability and electroplating method thereof
CN110923758B (en) * 2019-12-30 2023-10-27 东莞市斯坦得电子材料有限公司 High-buffering stability copper plating solution for PCB electroplating and preparation method thereof
CN112538643B (en) * 2020-11-17 2022-05-13 珠海松柏科技有限公司 High-speed tin plating additive and tin plating solution
CN115110126A (en) * 2022-06-14 2022-09-27 铜陵蔚屹新材料有限公司 Tin plating solution for tin plate of methanesulfonic acid system

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4459185A (en) * 1982-10-08 1984-07-10 Obata, Doni, Daiwa, Fine Chemicals Co., Ltd. Tin, lead, and tin-lead alloy plating baths
US4844780A (en) * 1988-02-17 1989-07-04 Maclee Chemical Company, Inc. Brightener and aqueous plating bath for tin and/or lead
EP1006217A1 (en) * 1998-12-03 2000-06-07 Lucent Technologies Inc. Tin electroplating process
CN1326015A (en) * 2000-03-31 2001-12-12 希普雷公司 Tin electrolyte
CN1420946A (en) * 2001-01-11 2003-05-28 株式会社日矿材料 Whisker-free tin or tin alloy plating solution, plating film and plated article
CN1550577A (en) * 2003-05-12 2004-12-01 罗姆和哈斯电子材料有限责任公司 Improved tin plating method
CN103029369A (en) * 2011-07-26 2013-04-10 罗门哈斯电子材料有限公司 High temperature resistant silver coated substrates

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4459185A (en) * 1982-10-08 1984-07-10 Obata, Doni, Daiwa, Fine Chemicals Co., Ltd. Tin, lead, and tin-lead alloy plating baths
US4844780A (en) * 1988-02-17 1989-07-04 Maclee Chemical Company, Inc. Brightener and aqueous plating bath for tin and/or lead
EP1006217A1 (en) * 1998-12-03 2000-06-07 Lucent Technologies Inc. Tin electroplating process
CN1326015A (en) * 2000-03-31 2001-12-12 希普雷公司 Tin electrolyte
CN1420946A (en) * 2001-01-11 2003-05-28 株式会社日矿材料 Whisker-free tin or tin alloy plating solution, plating film and plated article
CN1550577A (en) * 2003-05-12 2004-12-01 罗姆和哈斯电子材料有限责任公司 Improved tin plating method
CN103029369A (en) * 2011-07-26 2013-04-10 罗门哈斯电子材料有限公司 High temperature resistant silver coated substrates

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
甲基磺酸体系电镀锡及锡合金研究现状;张著等;《湖南有色金属》;20130430;第29卷(第2期);第36-39,76页 *
甲基磺酸盐电镀锡工艺及镀液性能;叶晓燕等;《腐蚀与防护》;20070831;第28卷(第8期);第422-424页 *
甲基磺酸盐镀锡添加剂研究进展;王腾等;《电镀与涂饰》;20090630;第28卷(第6期);第15-18页 *

Also Published As

Publication number Publication date
CN103882484A (en) 2014-06-25

Similar Documents

Publication Publication Date Title
CN103882484B (en) High-speed tin plating plating solution
CN103882485B (en) All-fulfate electrotinning additive and plating solution thereof
KR102028353B1 (en) Low internal stress copper electroplating method
CN101922026A (en) Methanesulfonic acid-based matte pure tin electroplating solution and additive thereof
Zhang et al. Preparation and corrosion performance of PEO coating with low porosity on magnesium alloy AZ91D in acidic KF system
SG175406A1 (en) High speed copper plating bath
KR20140033058A (en) Surface-treated steel sheet for battery cases, battery case, and battery
CN104630837A (en) Electroplating liquid and electroplating method of anthraquinone dye system acid copper plating
US20150225678A1 (en) Electrolytic copper foil, cleaning fluid composition and method for cleaning copper foil
CN110760902B (en) Tin electroplating solution and preparation method and application thereof
CN104805477A (en) Zinc plating liquid used for forming thick zinc coating as well as preparation method and application
KR20160127647A (en) Acid copper electroplating bath and method for electroplating low internal stress and good ductility copper deposits
Chen et al. Corrosion resistance of Ni/Cu/Ni–P triple-layered coating on Mg–Li alloy
CN103966640A (en) Method for preventing marine microbial corrosion by using artificial super-smooth surface
Liu et al. Adsorption orientation of sodium of polyaspartic acid effect on anodic films formed on magnesium alloy
CN110284163B (en) Copper plating solution for solar cell and preparation method thereof
Zhao et al. Corrosion behavior of anodized 7b50 aluminum alloy in different atmospheric environments
CN109579746A (en) A method of detection cold rolling electroplating tin steel plate passivating film
JP4742677B2 (en) Method for producing tin-plated steel strip
CN104593771A (en) Method for improving corrosion resistance of sintered NdFeB magnet through synergic protection of intergranular phosphating film and copper-plated coating and product
CN105297087A (en) Electroplating liquid for hydroxylamine reducing agent cyanide-free univalence copper plating and electroplating method
Nam et al. Quality reinforcement of electroplating zinc coatingselectrodeposited from cyanide free alkaline solution bypolyamine 70.000 and polyvinyl alcohol 16.000
Wang et al. A block copolymer as an effective additive for electrodepositing ultra-low Sn coatings
Runcheng et al. Electrochemical study on corrosion behaviors of P110 casing steel in a carbon dioxide-saturated oilfield formation water
CN105445178A (en) A test fluid for evaluating steel plate surface activity and a rapid measuring method

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20160629

CF01 Termination of patent right due to non-payment of annual fee