JPS6028917B2 - Manufacturing method of ultra-thin tin-plated steel sheet - Google Patents

Manufacturing method of ultra-thin tin-plated steel sheet

Info

Publication number
JPS6028917B2
JPS6028917B2 JP17802880A JP17802880A JPS6028917B2 JP S6028917 B2 JPS6028917 B2 JP S6028917B2 JP 17802880 A JP17802880 A JP 17802880A JP 17802880 A JP17802880 A JP 17802880A JP S6028917 B2 JPS6028917 B2 JP S6028917B2
Authority
JP
Japan
Prior art keywords
tin
ultra
amount
steel sheet
plated steel
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
Application number
JP17802880A
Other languages
Japanese (ja)
Other versions
JPS57101694A (en
Inventor
忠志 根本
亮一 福元
宏明 河村
嘉一 近藤
恒夫 乾
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.)
Toyo Kohan Co Ltd
Original Assignee
Toyo Kohan Co Ltd
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 Toyo Kohan Co Ltd filed Critical Toyo Kohan Co Ltd
Priority to JP17802880A priority Critical patent/JPS6028917B2/en
Publication of JPS57101694A publication Critical patent/JPS57101694A/en
Publication of JPS6028917B2 publication Critical patent/JPS6028917B2/en
Expired legal-status Critical Current

Links

Description

【発明の詳細な説明】 本発明は冷延鋼板上に電気亜鉛めつきを施したのち、ひ
きつづき0.05〜1.0夕/あの錫めつきを行うこと
により、極薄錫めつき鋼板の溶接性並びに半田性を改善
することを目的とするものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention is capable of producing ultra-thin tin-plated steel sheets by applying electrogalvanizing to a cold-rolled steel sheet and then continuing tinning for 0.05 to 1.0 minutes per minute. The purpose is to improve weldability and solderability.

従来から、容器材料として錫めつき鋼板すなわちぶりき
が広く用いられてきた。
Traditionally, tin-plated steel plate, or tinplate, has been widely used as a container material.

ぶりきは錫めつき量として1.12夕/で,2.8夕/
で,5.69/で,8.4夕/力あるいは11.2夕/
〆のものが使用され、表裏同一めつき量および差厚めつ
き量ものもが採用されているが、近年、高価な錫に替え
て、金属クロムとクロム水和酸化物を皮膜としたティン
フリ・スチール(TFS)が飲料缶用材料としてぶりき
に代って多量に使用され始めた。高価なぶりきから安価
なTFSへの切り替えが食缶分野で検討されているが、
内容物によっては耐食性に難点があり、錫の利点を生か
し、かつ錫量を大幅に減少させ、従来のぶりさより安価
な極薄錫めつき鋼板、例えば特開昭53−23833号
および特関昭53−26236号が提案され、当該業者
に注目されるようになってきた。一方、製缶分野におい
ては高価な錫を用いる半田缶に代って溶接による製缶が
最近使用され始め、安価なTFSの溶接缶が検討されて
いるものの高速熔接性に難点があり実用化に際しては種
々の問題がある。
The amount of tin plating for tinplate is 1.12 tinning and 2.8 tinning.
So, 5.69/, 8.4 evenings/power or 11.2 evenings/
The same plating amount and different plating thickness are used on both sides, but in recent years tin-free steel, which has a coating of metallic chromium and chromium hydrated oxide, has been used instead of expensive tin. (TFS) has begun to be used in large quantities as a material for beverage cans, replacing tin. Switching from expensive tinplate to cheaper TFS is being considered in the food can field.
Depending on the content, corrosion resistance may be a problem, so ultra-thin tin-plated steel sheets that take advantage of the advantages of tin, significantly reduce the amount of tin, and are cheaper than conventional tin plated steel sheets, such as JP-A No. 53-23833 and Tokuseki Akira No. 53-26236 was proposed, and it has started to attract attention from the concerned businesses. On the other hand, in the field of can manufacturing, welding cans have recently begun to be used instead of solder cans that use expensive tin, and although inexpensive welded TFS cans are being considered, they have difficulties in high-speed welding and have not been put into practical use. has various problems.

錫めつき鋼板はすぐれた溶接性を示すものであり、錫の
節約とすぐれた溶接性を兼ねそなえた極薄錫めつき鋼板
すなわち錫量が1.0夕/力以下の錫めつき鋼板が溶接
缶用として注目されようとしている。しかし極薄錫めつ
き鋼板の錫層は薄いため、半田性の他に溶接性が十分で
なく、高速溶接性に通した材料が強〈製缶業界において
要求されている。本発明は、前述のような問題点に鑑み
、冷延鋼板に少量の亜鉛を亀気めつきしたのち、1.0
タノで以下の錫を電気錫めつき浴中で浸債または電気め
つきにより被覆することによって、極薄錫めつき鋼板の
半田性の溶接性を改善するものである。
Tin-plated steel sheets exhibit excellent weldability, and ultra-thin tin-plated steel sheets that save tin and have excellent weldability, i.e., tin-plated steel sheets with a tin content of 1.0 mm/force or less, are It is starting to attract attention as a product for welded cans. However, since the tin layer of ultra-thin tin-plated steel sheets is thin, they do not have sufficient solderability or weldability, and materials with high-speed weldability are required in the can manufacturing industry. In view of the above-mentioned problems, the present invention has been developed by applying a small amount of zinc to a cold-rolled steel sheet, and then applying a coating of 1.0
The purpose is to improve the solderability and weldability of ultra-thin tin-plated steel sheets by coating them with the following tin by dipping or electroplating in an electric tinning bath.

一方、錫量が少なくなり、錫量が2.8夕/〆以下にな
ると半田性が劣下し、1.0夕/淋以下の錫量の極薄錫
めつき鋼板においては半田缶用途へは実用化が困難とさ
れている。容器業界においては依然として半田による製
缶法が多く用いられているため、溶接缶、半田缶のいず
れにも適用できる安価な材料が当該業者によって望まれ
ている。この要望に対して本発明は明確な解答を与え、
半田性と溶接性の改善によって従来錫量の少ない場合困
難とされていた半田缶への適用も可能とする極薄錫めつ
き鋼板を提供するものである。以下本発明を詳細に説明
する。
On the other hand, when the amount of tin decreases and the amount of tin becomes less than 2.8 min/gold, the solderability deteriorates, and ultra-thin tin-plated steel sheets with a tin content of less than 1.0 y/ml are used for solder cans. is said to be difficult to put into practical use. In the container industry, since can manufacturing methods using solder are still widely used, there is a desire by those in the industry for inexpensive materials that can be applied to both welded cans and soldered cans. The present invention provides a clear answer to this demand,
The present invention provides an ultra-thin tin-plated steel sheet that has improved solderability and weldability and can be applied to solder cans, which was conventionally considered difficult when the amount of tin was small. The present invention will be explained in detail below.

本発明に用いる電気亜鉛めつき浴は、酸性格およびアル
カリ格で、経済性および公害防止上、硫酸亜鉛を主成分
とする酸性格が適している。
The electrolytic galvanizing bath used in the present invention has acidic and alkaline properties, and acidic properties containing zinc sulfate as a main component are suitable from the viewpoint of economy and pollution prevention.

あらかじめ析出した亜鉛は錫めつき格に浸贋すると錫の
置換反応があるため、亜鉛が溶解し、錫めつき後特に浸
債によって錫めつきする場合は錫めつき前の亜鉛めつき
量より錫めつき後の亜鉛量は減少する。浸債錫めつきの
場合は、この亜鉛減少量に相当する錫が析出する。この
ため錫めつき後の必要亜鉛量となるように、減少亜鉛量
を考慮して電気亜鉛めつき量を決める。錫めつき後の亜
鉛量としては、亜鉛が0.005夕/め以上であいと、
溶接性および半田性が改善されない。
When pre-precipitated zinc is immersed into a tin plating plate, there is a substitution reaction of tin, so the zinc dissolves and after tinning, especially when tin plating is done by dipping, the amount of zinc plating before tinning is smaller than that before tinning. The amount of zinc decreases after tinning. In the case of bond immersion tin plating, tin corresponding to this amount of zinc reduction is precipitated. For this reason, the amount of electrolytic galvanizing is determined in consideration of the reduced amount of zinc so that the amount of zinc is required after tinning. As for the amount of zinc after tin plating, if the zinc content is 0.005 mm/metre or more,
Weldability and solderability are not improved.

また、亜鉛が0.2タノ〆を越えると、溶接性および半
田性が低下し、また、亜鉛の腐食による白錆が発生する
ので、亜鉛量としては0.005〜0.2夕/わが好ま
しい。錫めつきとしては、生産性および作業性の面で電
気錫めつき格を用いることが好ましく、電気錫めつき浴
としては硫酸錫を用いる酸性格、錫酸ソーダを用いるア
ルカリ浴および塩化第1錫を用いるハロゲン浴が適して
いる。
Furthermore, if the zinc content exceeds 0.2 mm, weldability and solderability will deteriorate, and white rust will occur due to zinc corrosion, so the zinc amount is preferably 0.005 to 0.2 mm/cm. . For tinning, it is preferable to use an electric tinning bath from the viewpoint of productivity and workability.As for the electric tinning bath, an acid bath using tin sulfate, an alkaline bath using sodium stannate, and a dichloride bath are preferable. A halogen bath using tin is suitable.

錫めつきの方法としては上述の電気錫めつき裕中で無電
解浸漬めつきを施すか、または電気めつきを施す。浸債
の場合は、冷延鋼板にあらかじめ電気亜鉛めつきにより
析出した亜鉛が電気錫めつき裕中の錫と反応して、錫が
置換析出することを利用できる。浸漬時間は数秒以内の
短時間で錫を析出させることができ、浸濃時間および亜
鉛めつき軍により、析出錫量を調節できる。電気錫めつ
きの場合は陰極電解によって行い、電流効率と電気量に
より錫量を制御することができる。錫のめつき量として
は、錫が0.05夕/め以上でないと、溶接が難しく、
また亜鉛の腐食による白錆防止に効果がない。
As a method of tinning, electroless immersion plating is performed in the above-mentioned electric tinning bath, or electroplating is performed. In the case of bond dipping, it is possible to utilize the fact that zinc precipitated on a cold-rolled steel sheet by electrogalvanizing reacts with tin in the electrolytic tinning, and tin is precipitated by displacement. Tin can be precipitated within a short immersion time of several seconds, and the amount of precipitated tin can be adjusted by adjusting the immersion time and the strength of galvanizing. In the case of electrolytic tinning, cathodic electrolysis is used, and the amount of tin can be controlled by current efficiency and amount of electricity. Welding is difficult unless the amount of tin plating is at least 0.05 mm/metre.
Also, it is not effective in preventing white rust caused by corrosion of zinc.

また、錫量が1.0夕/めを越えると、安価な容器材料
を提供できない。したがって、0.05〜1.0夕/あ
の錫量によって本発明の目的である溶酸性および半田性
にすぐれた安価な極薄錫めつき鋼板を提供できる。半田
缶用途に対しては、錫量が増加するにしたがって半田性
および溶接性は向上するので好ましくは0.3〜1.0
タノあの範囲がよい。無電解浸債錫めつき浴中の2価ま
たは4価錫イオンが、0.2夕/そ以上でないと、前め
つきにより析出した亜鉛との置換反応がすみやかに起り
にくく、50タノ〆を越えると経済的でないので、2価
または4価錫イオンは0.2〜50夕/そが好ましい。
Moreover, if the amount of tin exceeds 1.0 m/m, it is not possible to provide an inexpensive container material. Therefore, with an amount of tin of 0.05 to 1.0 m/m, it is possible to provide an inexpensive ultra-thin tin-plated steel sheet with excellent acid solubility and solderability, which is the object of the present invention. For solder can applications, the solderability and weldability improve as the amount of tin increases, so it is preferably 0.3 to 1.0.
Tano that range is good. If the divalent or tetravalent tin ion in the electroless tin plating bath is not more than 0.2 m/m, the substitution reaction with the zinc precipitated by pre-plating will not occur quickly, and the Since it is not economical to use more than 0.2 to 50 m/s of divalent or tetravalent tin ion.

pH7以下の酸性の格では硫酸第1錫、ホウ弗化錫、塩
化第1錫あるいは袴酸第1錫により2価錫イオンが供給
される。pH7を越えるアルカリ性格の場合は錫酸ナト
リウムあるいは錫酸カリウムにより、4価錫イオンを供
給する。硫酸第1錫を用いる場合は硫酸俗とし、ホウ弗
化錫および塩化第1錫の場合は弗化物格が通し、修酸第
1錫の場合、鯵酸浴が適している。錫酸ナトリウムおよ
び錫酸カリウムにおいては水酸化ナトリウムを含む格が
適している。またアルカリ性格で塩化第1錫を用いると
きは水酸化ナトリウム格を用いることができる。錫めつ
き鋼板の場合、錫層を溶融することにより、錫は光沢を
有する表面になるので、本発明は光沢を要求される用途
に対しては錫層を溶融するりフロー処理を行うことがで
きる。
In acid conditions of pH 7 or lower, divalent tin ions are supplied by stannous sulfate, tin borofluoride, stannous chloride, or stannous hakamate. If the pH is alkaline and exceeds 7, tetravalent tin ions are supplied using sodium stannate or potassium stannate. When using stannous sulfate, it is suitable as sulfuric acid, when using tin borofluoride and stannous chloride, the fluoride group is suitable, and when using stannous oxalate, a boron acid bath is suitable. For sodium stannate and potassium stannate, a grade containing sodium hydroxide is suitable. Furthermore, when using stannous chloride with alkaline properties, sodium hydroxide can be used. In the case of tin-plated steel sheets, melting the tin layer gives the tin a glossy surface, so for applications that require gloss, the present invention can melt the tin layer or perform flow treatment. can.

通常の電気めつきぶりきは、めつき後直ちに、あるし、
はめつき後リフロー処理し、急冷したのち、重クロム酸
ナトリウム等で不動態化処理が施されるが、本発明にお
いてもこの処理が適用できる。
Normal electroplating is done immediately after plating,
After fitting, a reflow treatment is performed, and after rapid cooling, a passivation treatment is performed using sodium dichromate, etc., and this treatment can also be applied to the present invention.

通常のクロム酸系の処理の場合のクロム付着量はlo夕
/め以下で問題は生じない。なお、クロム系を用いない
、リン酸、リン酸塩および炭酸ナトリウム等の処理も用
いることができる。その他後処理としては他の方法もあ
るが特に後処理方法を限定するものではない。また、後
処理を施さない場合も適用できる。以下、本発明を実施
例により、具体的に説明する。
In the case of ordinary chromic acid-based treatment, the amount of chromium deposited is less than 100% and no problem occurs. Note that treatments that do not use chromium, such as phosphoric acid, phosphates, and sodium carbonate, can also be used. There are other post-processing methods, but the post-processing methods are not particularly limited. It can also be applied without post-processing. EXAMPLES Hereinafter, the present invention will be specifically explained with reference to Examples.

実施例 1 0.22肋の冷延鋼板を7%のか性ゾーダ溶液中で電解
脱脂し、水洗し、3%の硫酸溶液中で電解酸洗し、水洗
したのち、次に示す組成および処理条件で、0.03夕
/めの電気亜鉛めつきを施し、水洗したのち、次に示す
組成の錫めつき裕中に無電解浸潰し、0.13夕/あの
錫めつきを行ない、30夕/その車クロム酸ナトリウム
溶液中で陰極処理したのち、ジ・オクチル・セバケート
(以下DOSという)を塗減した。
Example 1 A 0.22 rib cold rolled steel plate was electrolytically degreased in a 7% caustic Soda solution, washed with water, electrolytically pickled in a 3% sulfuric acid solution, washed with water, and then given the following composition and treatment conditions. After electrolytic galvanizing for 0.03 pm/day, washing with water, electroless immersion in a tin plating bath having the following composition, tin plating for 0.13 pm, and 30 pm /After the car was cathodically treated in a sodium chromate solution, di-octyl sebacate (hereinafter referred to as DOS) was applied.

錫めつき後の亜鉛付着量は0.009夕/めであった。
電気蓮鉛めつきの裕組成および処理条件 俗組成 硫酸亜鉛 300夕/そ硫酸ナト
リウム 75タノク硫酸アルミニウム 25
夕/そ 処理条件 俗温 4000処理電気量
1クーロン/dで錫めつき格の俗組成およ
び処理条件 浴組成 硫酸錫 60夕/夕フェノールス
ルフオン酸 30夕/そエトキシ化Qナフトール
スルフオン酸 5タノク 処理条件 格温 4500浸債時間
1秒実施例 2 実施例1と同様の前処理を行ない、次に示す組成および
処理条件で0.03夕/あの電気亜鉛めつきを施し、水
洗したのち、次に示す組成および処理条件で0.41夕
/めの錫めつきを行ない、30多/その重クロム酸ナト
リウム溶液中で陰極処理したのち、DOSを塗油した。
The amount of zinc deposited after tin plating was 0.009 mm/metre.
Composition and processing conditions for electrolytic lotus lead plating Zinc sulfate 300/Sodium sulfate 75 Tanok aluminum sulfate 25
Evening/Sono Processing Conditions Normal Temperature 4000 Processing Electricity
Typical composition and processing conditions for tin plating at 1 coulomb/d Bath composition Tin sulfate 60/day Phenolsulfonic acid 30/So Ethoxylation Q Naphtholsulfonic acid 5 Tanok Processing conditions Temperature 4500 Soaking time
1 second Example 2 The same pretreatment as in Example 1 was carried out, and electrogalvanizing was performed for 0.03 minutes using the composition and treatment conditions shown below. After washing with water, After 41 days of tin plating and cathodic treatment in 30 days of sodium dichromate solution, DOS was applied.

錫めつき後の亜鉛付着量は0.01多/めであった。電
気亜鉛めつきの格組成および処理条件 裕組成 硫酸亜鉛 300夕/そ硫酸ナトリ
ウム 75夕/そ硫酸アルミニウム
25夕/そ処理条件格温
4000処理電気量 1クーロン
/d力錫めつき格の格組成および処理条件 裕組成 硫酸錫 60夕/夕フエノール
スルフオン 30夕/そエトキシ化Qナフトー
ルスルフオン酸 59/夕 処理条件 (無電解浸債処理後、電解処理) 俗温 4500浸糟時間
0.9沙処理電気量
3クーロン/dで実施例 3 実施例1と同様の前処理を行ない、次に示す組成および
処理条件で0.14夕/めの電気亜鉛めつきを施し、水
洗したのち、次に示す組成および処理条件で0.64夕
/あの錫めつきを行ない、リフローし、錫を溶融したの
ち、30タノクの重クロム酸ナトリウム溶液中で陰極処
理したのち、DOSを塗油した。
The amount of zinc deposited after tin plating was 0.01%. Electrogalvanizing grade composition and processing conditions Weak composition Zinc sulfate 300 t/Sodium sulfate 75 t/Aluminum sulfate
25th evening/So processing conditions: temperature
4000 Processing electricity amount 1 coulomb/d force Tin plating grade composition and processing conditions Rich composition Tin sulfate 60 evenings/day Phenolsulfonate 30 evenings/so Ethoxylation Q Naphtholsulfonic acid 59/day Treatment conditions (electroless immersion After bond processing, electrolytic treatment) Ordinary temperature 4500 soaking hours
0.9sa processing electricity amount
Example 3 The same pretreatment as in Example 1 was carried out at 3 coulombs/d, and electrogalvanizing was performed at 0.14 coulombs/day using the composition and treatment conditions shown below. After washing with water, the following composition and treatment conditions were applied: Tin plating was carried out at 0.64 pm under processing conditions, reflowed and the tin melted, cathodically treated in a 30 ton solution of sodium dichromate, and then coated with DOS.

錫めつき後の亜鉛付着量は0.14夕/めであった。電
気亜鉛めつきの裕組成および処理条件 電気亜鉛めつきの浴組成および処理条件 裕組成 硫酸錫亜鉛 250夕/そ硫酸アンモ
ニウム 80夕/そ硫酸ナトリウム
50夕/そ棚酸 3
09/〆処理条件 俗温 40こ○処理電気量
4クーロン/d力錫めつき俗の浴組成およ
び処理条件 裕組成 硫酸錫 4M/そ フェノールスルフオン酸 30タノクエトキシ化Q
ナフトールスルフ オン酸 5夕/そ 処理条件 俗温 45o0処理電気量
12クーロン/d〆実施例 4 実施例1と同様の前処理を行ない、次に示す組成および
処理条件で0.17夕/〆の電気亜鉛めつきを施し、水
洗したのち、次に示す組成および処理条件で0.11夕
/あの錫めつきを行ない、30夕/その重クロム酸ナト
リウム溶液中で陰極処理したのち、DOSを塗油した。
The amount of zinc deposited after tin plating was 0.14 mm/metre. Weak composition and treatment conditions for electrogalvanizing Bath composition and treatment conditions for electrogalvanizing Weak composition: tin zinc sulfate 250 t/ammonium sulfate 80 t/sodium sulfate
50 evenings/sodana acid 3
09/〆Processing conditions Normal temperature 40゜Processing electricity amount
4 coulombs/d force Tin plating common bath composition and processing conditions Composition tin sulfate 4M/phenol sulfonic acid 30 tanoxethoxylated Q
Naphtholsulfonic acid 5 nights/so Processing conditions Normal temperature 45o0 Processing electricity amount 12 coulombs/d〆Example 4 The same pretreatment as in Example 1 was carried out, and the following composition and treatment conditions were used for 0.17 nights/〆 After electrolytic galvanizing and washing with water, tin plating was carried out for 0.11 evenings using the following composition and processing conditions, and after cathodic treatment in the sodium dichromate solution for 30 evenings, DOS was applied. It was oiled.

錫めつき後の亜鉛付着量は0.17夕/めであった。電
気亜鉛めつきの裕組成および処理条件 浴組成 硫酸亜鉛 380夕/そ硫酸ナトリ
ウム 72夕/そ硫酸マグネシウム
61夕/そ処理条件 俗温 60qo処理電気量
5クーロン/dで実施例 5 実施例1と同様の前処理を行ない、次に示す組成および
処理条件で0.01夕/あの電気頭鉛めつきを施し、水
洗したのち、次に示す組成および処理条件で0.45タ
ノあの錫めつきを行ない、30夕/その重クロム酸ナト
リウム溶液で陰極処理したのち、DOSを塗油した。
The amount of zinc deposited after tin plating was 0.17 mm/metre. Electrogalvanizing composition and processing conditions Bath composition Zinc sulfate 380 t/Sodium sulfate 72 t/Magnesium sulfate
61 evening/so Processing conditions Normal temperature 60qo Processing amount of electricity
Example 5 The same pretreatment as in Example 1 was carried out at 5 coulombs/d, followed by electroplating with the following composition and treatment conditions at 0.01 t/d, followed by washing with water. Tin plating was carried out at 0.45 mm under treatment conditions, and after 30 evenings of cathodic treatment with the sodium dichromate solution, DOS was applied.

錫めつき後の亜鉛付着量は0.01夕/めであった。電
気亜鉛めつきの俗組成および処理条件 裕組成 塩化亜鉛 200夕/そ塩化アンモ
ニウム 250夕/そ塩化ナトリウム
80夕/そ弗化ナトリウム 5夕
/そ 処理条件 浴温 35q0処理電気量
0.3クーロン/d〆錫めつき格の組成およ
び処理条件塩化第1錫 75夕/そ塩
化ナトリウム 45夕/ク弗化ナトリウム
25夕/そ弗化水素カリウム
5M/そ 処理条件 俗温 65oo浸債時間
0.9砂処理電気量
3クーロン/dで実施例 6 実施例1と同様の前処理を行ない、次に示す組成および
処理条件で0.02/枕電気亜鉛めつきを施し、水洗し
たのち、次に示す組成および処理条件で0.43夕/あ
の錫めつきを行ない、30夕/その重クロム酸ナトリウ
ム溶液で陰極処理したのち、DOSを塗油した。
The amount of zinc deposited after tin plating was 0.01 mm/metre. Common composition and processing conditions for electrogalvanizing: Zinc chloride 200 t/s Ammonium chloride 250 t/s Sodium chloride
80 evenings/so Sodium fluoride 5 evenings/so Treatment conditions Bath temperature: 35 q0 Processing electricity amount 0.3 coulombs/d Tin plating composition and treatment conditions Stannous chloride 75 evenings/Sodium chloride 45 evenings/Ku Sodium
25th evening/potassium hydrogen fluoride
5M/so Processing conditions normal temperature 65oo bonding time
0.9 Sand processing electricity amount
Example 6 The same pretreatment as in Example 1 was carried out at 3 coulombs/d, and 0.02/pillow electrogalvanization was performed with the following composition and treatment conditions, and after washing with water, the following composition and treatment conditions were applied. After 0.43 evenings of tin plating, and 30 evenings of cathodic treatment with the sodium dichromate solution, DOS was applied.

錫めつき後の亜鉛付着量は0.02夕/めであった。電
気亜鉛めつきの裕組成および処理条件 俗組成 硫酸亜鉛 350夕/そ硫酸アンモ
ニウム 30夕/そ処理条件 格温 4500処理電気量
0.6クーロン/d力錫めつきの裕組成およ
び処理条件格組成 錫酸ナトリウム 100夕/そ水酸化ナト
リウム 159/そ処理条件俗温
85oo処理電気量
15クーロン/dの比較例 1実施例1と同様の前処理
を行ない、次に示す組成および処理条件で0.7夕/力
の錫めつきを施し、リフロ−を行ない、錫を溶融したの
ち、30夕/その重クロム酸ナトリウム溶液中で陰極処
理し、DOSを塗油した。
The amount of zinc deposited after tin plating was 0.02 mm/metre. Composition and processing conditions for electrolytic galvanizing General composition Zinc sulfate 350 t/ammonium sulfate 30 t/s Processing conditions Rating temperature 4500 Processing electricity 0.6 coulombs/d force Wearing composition and processing conditions for tin plating Rating composition Sodium stannate 100/Sodium hydroxide 159/So Processing conditions Normal temperature
85oo processing electricity amount
Comparative example of 15 coulombs/d 1 Perform the same pretreatment as in Example 1, apply tinning at 0.7 coulombs/force under the composition and treatment conditions shown below, perform reflow, and melt the tin. , 30 evening/cathode treatment in the sodium dichromate solution and oiling with DOS.

錫めつきの格組成および処理条件 浴組成 硫酸錫 60夕/夕フェノールス
ルフオン酸 30夕/そェトキシ化Qナフトール
スルフオン酸5夕/夕 処理条件 浴温 4500処理電
気量 20クーロン/d〆比較例 2実施例
1と同様の前処理を行ない、比較例1と同様に0.7夕
/あの錫めつきを行ない、30夕/その車クロム酸ナリ
ウム溶液中で陰極処理し、DOSを塗油した。
Tin plating case composition and treatment conditions Bath composition Tin sulfate 60 t/t Phenolsulfonic acid 30 t/t Oxylated Q naphtholsulfonic acid 5 t/t Treatment conditions Bath temperature 4500 Processing electricity amount 20 coulombs/d〆 Comparative example 2 The same pretreatment as in Example 1 was carried out, the tin plating was carried out in the same manner as in Comparative Example 1 for 0.7 evenings, and the car was cathodically treated in a sodium chromate solution for 30 evenings, and the car was coated with DOS. .

実施例1〜6,比較例1および2で得られた錫めつき鋼
板について、次に示す半田入り性、塩水頃霧試験、室内
暴露による耐錆性試験および溶接性試験を行った。
The tin-plated steel plates obtained in Examples 1 to 6 and Comparative Examples 1 and 2 were subjected to the following solderability, salt water fog test, rust resistance test by indoor exposure, and weldability test.

{1} 半田入り性試験 75肋×25肌の長方形の試片を切りだし、短辺を折り
曲げ、その断面を平行となるようにした。
{1} Solderability test A rectangular specimen of 75 ribs x 25 skins was cut out, and the short sides were bent so that the cross section was parallel.

これをフラックス中に5肌の深さに浸潰したのち、29
0℃の純錫半田裕中に垂直に1分間浸潰し、試片を取り
出し水中で急冷した。試片の折り目を開いて、半田俗の
表面から毛細管現象で上昇した半田の高さを半田入り性
として評価した。半田入り性は上昇した半田の高さが高
い程優れている。■ 室内暴露による発錆試験 屋内に4週間暴露したのち、発錆状態を調べ、鈴発生面
積率により評価した。
After soaking this in flux to a depth of 5 skin, 29
The sample was vertically immersed in pure tin solder solution at 0° C. for 1 minute, and the sample was taken out and rapidly cooled in water. The crease of the specimen was opened, and the height of the solder rising from the solder surface due to capillary action was evaluated as solderability. The higher the height of the raised solder, the better the solderability. ■ Rust test by indoor exposure After being exposed indoors for 4 weeks, the state of rust was examined and evaluated based on the area ratio of rust occurrence.

数値の低いもの程耐食性が懐れている。糊 溶接性試験 試料を210℃,15分間加熱したのち、試験用溶接機
を用いて、周波数60HZ,ラップ幅0.4肋,速度7
.2の/分、加圧力45k9/嫌の条件で溶接第 1
表 注11)屋内暴露試験:錆発生面積率を示す。
The lower the number, the better the corrosion resistance. Glue After heating the weldability test sample at 210°C for 15 minutes, welding was performed using a test welding machine at a frequency of 60Hz, a lap width of 0.4, and a speed of 7.
.. Welding No. 1 under the conditions of 2 min/min and a pressure of 45 k9/min.
Table note 11) Indoor exposure test: Shows the rust occurrence area rate.

■ 溶接性:溶接可能電流範囲を示す。を行った。■ Weldability: Indicates the weldable current range. I did it.

電気抵抗加熱による溶接時のスプラッシュ(過熱による
溶融鉄のとびちり)を起さない最大電流と漏えいを起さ
ない溶接強度の得られる最小電流を測定した。この差を
溶接可能電流範囲とした。この範囲の大きいもの程溶接
性が優れている。この溶接可能電流範囲を測定した。
The maximum current that would not cause splash (molten iron sputtering due to overheating) during welding by electric resistance heating and the minimum current that would provide welding strength that would not cause leakage were measured. This difference was defined as the weldable current range. The larger this range is, the better the weldability is. This weldable current range was measured.

第1表に示すように、本発明の方法による極薄錫めつき
鋼板は、優れた半田入り性、および溶接性を有すること
が認められた。
As shown in Table 1, the ultra-thin tin-plated steel plate produced by the method of the present invention was found to have excellent solderability and weldability.

Claims (1)

【特許請求の範囲】 1 極薄錫めつき鋼板の製造方法において、冷延鋼板の
片面または両面に、錫めつき後の亜鉛量が0.005〜
0.2g/m^2の電気亜鉛めつきを施した後、錫量0
.05〜1.0g/m^2の電気錫めつきを施すことを
特徴とする極薄錫めつき鋼板の製造法。 2 極薄錫めつき鋼板の製造方法において、冷延鋼板の
片面または両面に、錫めつき後の亜鉛量が0.005〜
0.2g/m^2になるように電気亜鉛めつきを施した
後、錫量0.05〜1.0g/m^2の無電解浸漬錫め
つきを施すことを特徴とする極薄錫めつき鋼板の製造法
。 3 無電解浸漬錫めつきの浴が、2価錫イオンを0.2
〜50g/l含む酸性錫めつき浴または4価錫イオンを
0.2〜50g/l含むアルカリ錫めつき浴である特許
請求の範囲第2項記載の極薄錫めつき鋼板の製造法。 4 極薄錫めつき鋼板の製造方法において、冷延鋼板の
片面または両面に、錫めつき後の亜鉛量が0.005〜
0.2g/m^2になるように電気亜鉛めつきを施した
後、無電解浸漬錫めつきにつづいて電気錫めつきを、錫
量0.05〜1.0g/m^2の範囲で施すことを特徴
とする極薄錫めつき鋼板の製造法。 5 無電解浸漬錫めつきの浴が、2価錫イオンを0.2
〜50g/lを含む酸性錫めつき浴または4価錫イオン
を0.2〜50g/lを含むアルカリ錫めつき浴である
特許請求の範囲第4項記載の極薄錫めつき鋼板の製造方
法。
[Claims] 1. In a method for producing an ultra-thin tin-plated steel sheet, the amount of zinc after tin-plating is 0.005 to 0.05 on one or both sides of the cold-rolled steel sheet.
After electrogalvanizing at 0.2g/m^2, the amount of tin is 0.
.. A method for producing an ultra-thin tin-plated steel sheet, characterized by applying electro-tinning of 0.05 to 1.0 g/m^2. 2. In the method for producing ultra-thin tin-plated steel sheets, the amount of zinc after tin-plating is 0.005 to 0.05 on one or both sides of the cold-rolled steel sheet.
Ultra-thin tin characterized by electroless galvanizing to a tin content of 0.2 g/m^2 and then electroless immersion tinning with a tin content of 0.05 to 1.0 g/m^2. Manufacturing method for galvanized steel sheets. 3 Electroless immersion tin plating bath absorbs 0.2 divalent tin ions.
The method for producing an ultra-thin tin-plated steel sheet according to claim 2, which is an acidic tin plating bath containing ~50 g/l or an alkaline tin plating bath containing 0.2 to 50 g/l of tetravalent tin ions. 4. In the method for producing an ultra-thin tinned steel sheet, the amount of zinc after tinning is 0.005 to 0.005 on one or both sides of the cold rolled steel sheet.
After electrolytic galvanizing to a concentration of 0.2 g/m^2, electroless immersion tinning was followed by electrolytic tinning to a tin amount of 0.05 to 1.0 g/m^2. A method for producing ultra-thin tin-plated steel sheets. 5 The electroless immersion tin plating bath absorbs 0.2 divalent tin ions.
Production of an ultra-thin tin-plated steel sheet according to claim 4, which is an acidic tin plating bath containing ~50 g/l or an alkali tin plating bath containing 0.2-50 g/l of tetravalent tin ions. Method.
JP17802880A 1980-12-18 1980-12-18 Manufacturing method of ultra-thin tin-plated steel sheet Expired JPS6028917B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17802880A JPS6028917B2 (en) 1980-12-18 1980-12-18 Manufacturing method of ultra-thin tin-plated steel sheet

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17802880A JPS6028917B2 (en) 1980-12-18 1980-12-18 Manufacturing method of ultra-thin tin-plated steel sheet

Publications (2)

Publication Number Publication Date
JPS57101694A JPS57101694A (en) 1982-06-24
JPS6028917B2 true JPS6028917B2 (en) 1985-07-08

Family

ID=16041317

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17802880A Expired JPS6028917B2 (en) 1980-12-18 1980-12-18 Manufacturing method of ultra-thin tin-plated steel sheet

Country Status (1)

Country Link
JP (1) JPS6028917B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0320014Y2 (en) * 1985-07-02 1991-04-30

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2126249B (en) * 1982-09-03 1986-01-08 Toyo Kohan Co Ltd Process for producing a thin tin and zinc plated steel sheet
US4508601A (en) * 1982-09-07 1985-04-02 Toyo Kohan Co., Ltd. Process for producing a thin tin and zinc plated steel sheet
GB2157319A (en) * 1984-04-13 1985-10-23 Toyo Kohan Co Ltd Tin free steel and its production
NL189310C (en) * 1984-05-18 1993-03-01 Toyo Kohan Co Ltd COATED STEEL SHEET WITH IMPROVED WELDABILITY AND METHOD FOR MANUFACTURING.
JPS6119793A (en) * 1984-07-03 1986-01-28 Sumitomo Metal Ind Ltd Surface treated steel plate excellent in solderability

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0320014Y2 (en) * 1985-07-02 1991-04-30

Also Published As

Publication number Publication date
JPS57101694A (en) 1982-06-24

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