[go: up one dir, main page]

JPS59173167A - Method for treating substrate of painting - Google Patents

Method for treating substrate of painting

Info

Publication number
JPS59173167A
JPS59173167A JP4759383A JP4759383A JPS59173167A JP S59173167 A JPS59173167 A JP S59173167A JP 4759383 A JP4759383 A JP 4759383A JP 4759383 A JP4759383 A JP 4759383A JP S59173167 A JPS59173167 A JP S59173167A
Authority
JP
Japan
Prior art keywords
zinc phosphate
phosphate treatment
treated
painting
treating
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.)
Pending
Application number
JP4759383A
Other languages
Japanese (ja)
Inventor
Nobuhiro Ito
伊藤 信広
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.)
Toyota Motor Corp
Original Assignee
Toyota Motor Corp
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 Toyota Motor Corp filed Critical Toyota Motor Corp
Priority to JP4759383A priority Critical patent/JPS59173167A/en
Publication of JPS59173167A publication Critical patent/JPS59173167A/en
Pending legal-status Critical Current

Links

Landscapes

  • Application Of Or Painting With Fluid Materials (AREA)

Abstract

PURPOSE:To prevent rusting on an object to be treated stagnating near a zinc phosphate treating tank in the substrate treating stage of a phosphate film by specifying the amt. of the nitrite ion in the zinc phosphate treating liquid. CONSTITUTION:The amt. of the nitrite ion to be added in a zinc phosphate treating liquid is regulated to >=1.0X10<-3>M/l and <=2.5X10<-3>M/l in a method for substrate treating method of painting by which a phosphate film is formed on the surface of an object to be treated. Then the excess nitrite ion is discharged in the form of ammonia, nitrous acid, etc. to the outside of the system and the rusting on the material to be treated is prevented by the effect of neutralizing the atmosphere hear the zinc phosphate treating tank and the effect of forming a slightly non-conductive film on the surface of the object to be treated.

Description

【発明の詳細な説明】 この発明は、被処理物表面にリン酸塩被膜を形成して塗
装下地処理を行なう方法に関し、特に、塗装下地処理工
程及びその前後において停滞する被処理物の発錆を防止
する方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method of forming a phosphate film on the surface of a workpiece to treat the surface of the workpiece for painting, and in particular, to prevent rusting of the workpiece that stagnates during the basework treatment process and before and after the process. Regarding how to prevent this.

従来より、車両等の塗装下地処理としてリン酸塩処理、
特にリン酸亜鉛処理が広く行なわれている。このリン酸
亜沿処理工程には1通常、コンベア等を用いた連vc処
□理方式が適用され、作業1!シ率。
Traditionally, phosphate treatment has been used as a base treatment for painting vehicles, etc.
In particular, zinc phosphate treatment is widely used. For this phosphoric acid treatment process, a continuous VC treatment method using a conveyor or the like is usually applied. Shi rate.

安全性の向上が図られている。しかしながら、このよう
にコンベア等を用いた連続処理を行なう場合、リン酸亜
鉛処理の前後工程における事情やコンベアトラブル等に
起因して、被処理物がリン酸亜鉛処理層の近辺において
停滞することがある。
Efforts are being made to improve safety. However, when carrying out continuous processing using a conveyor, etc., the treated material may stagnate near the zinc phosphate treatment layer due to circumstances before and after the zinc phosphate treatment, conveyor troubles, etc. be.

一方、リン酸亜鉛処理液は、化成性の面から各成分の組
成が決定されるが、通常、リン酸イオン、亜鉛イオン、
塩素酸イオンまたは硝酸イオン、及び亜硝酸イオン等を
主成分として、強酸性の性状を有するものであり、その
リン酸亜鉛処理槽の近辺が強度の腐蝕性雰囲気であるこ
とから、上述のように被処理物がリン酸亜鉛処理槽近辺
において停滞すると、停滞する被処理物は短時間で容易
に発錆し、発錆した被処理物は廃棄せざるを得なかった
On the other hand, the composition of each component of the zinc phosphate treatment solution is determined from the viewpoint of chemical conversion, but usually phosphate ions, zinc ions,
It has strong acidic properties, mainly consisting of chlorate ions, nitrate ions, nitrite ions, etc., and the vicinity of the zinc phosphate treatment tank is a highly corrosive atmosphere, so as mentioned above, When the treated material stagnates near the zinc phosphate treatment tank, the stagnant treated material easily rusts in a short period of time, and the rusted treated material has to be discarded.

従来、このような事態を防止し、あるいは緩和するため
に以下のような対策が講じられていた。
Conventionally, the following measures have been taken to prevent or alleviate such situations.

第1に、リン酸亜鉛処理槽近辺及びリン酸亜鉛処理工程
の前後工程における吸排気を強化し、雰囲気を正常化す
る方法があった。また第2にリン酸亜鉛処理槽近辺にお
いて停滞する被処理物に対して、アルカリ性液または防
錆剤溶液のミストシャワーを行ない、発錆を抑制する方
法があった。
First, there was a method of normalizing the atmosphere by strengthening the air intake and exhaust in the vicinity of the zinc phosphate treatment tank and before and after the zinc phosphate treatment process. A second method is to perform a mist shower of an alkaline solution or a rust preventive solution on the workpieces stagnant in the vicinity of the zinc phosphate treatment tank to suppress rust formation.

しかし、上記第1の方法にあっては、リン酸亜鉛処理前
の被処理物が過剰に乾燥し、リン酸亜鉛処理を行う際に
、処理ムラを発生するという欠点があり、上記第2の方
法にあっては、被処理物に付着したアルカリ性液または
防錆剤溶液がリン酸亜鉛処理液中に持込まれ、リン酸亜
鉛処理液が汚染されるという欠点があった。
However, the first method described above has the disadvantage that the object to be treated before the zinc phosphate treatment dries excessively, resulting in uneven treatment when the zinc phosphate treatment is performed. This method has the disadvantage that the alkaline liquid or rust preventive solution adhering to the object to be treated is carried into the zinc phosphate treatment solution, thereby contaminating the zinc phosphate treatment solution.

以上の欠点をカバーするために、上記従来方法において
は、吸排気の強化を行うにしても、あるいは、アルカリ
性液や防錆剤溶液のミストシャワーを行うにしても、そ
の程度を緩和せざるを得ず、その結果上記従来方法を採
る場合においては、コンベアトラブル等に起因して被処
理物が停滞しても、被処理物の状態が良好に保たれる時
間すなわち、停滞許容時間を長くすることは困難であり
、その停滞許容時間としては約10分間程度が限度とな
っていた。
In order to overcome the above-mentioned drawbacks, in the conventional method described above, even if the intake and exhaust are strengthened or a mist shower of alkaline liquid or rust preventive solution is performed, the degree of influence must be relaxed. As a result, when the above conventional method is adopted, the time during which the condition of the workpiece can be maintained in good condition even if the workpiece is stagnant due to conveyor trouble, that is, the allowable stagnation time is lengthened. It is difficult to do so, and the allowable stagnation time is limited to approximately 10 minutes.

そのため、上記従来方法を行なう場合、停滞許容時間が
短時間であることから、短時間で復旧するコンベア・ト
ラブル等には効果がある反面以下の様な不都合が生じる
。すなわち、第1に、塗装下地処理工程を前後の機械加
工・組付工程及び塗装工程と共に一連の連続工程とする
場合、作業員の休息時間等の機械運転停止時間には、リ
ン酸亜鉛処理槽近辺の強酸性雰囲気中に停滞許容時間を
越えて被処理物を放置することになり、それによる被処
理物の発錆・廃棄が避けがたく、そのため、上述の一連
の連続工程化は不可能である。第2に短時間では復旧し
ないコンベアトラブルが発生した場合、被処理物が停滞
許容時間を越えて前述の強酸性雰囲気中に停滞し、その
ため発錆し、廃棄せざるを得ないという事態が生じる。
Therefore, when the above conventional method is used, since the permissible stagnation time is short, it is effective for troubleshooting conveyor problems that can be recovered in a short period of time, but on the other hand, the following disadvantages occur. Firstly, when the painting base treatment process is a series of continuous processes together with the preceding and succeeding machining/assembly processes and painting processes, the zinc phosphate treatment tank is The workpiece will be left in a nearby strongly acidic atmosphere for longer than the allowable stagnation time, which will inevitably lead to rusting and disposal of the workpiece, making it impossible to implement the series of continuous processes described above. It is. Second, if a conveyor problem occurs that cannot be resolved in a short time, the objects to be processed will stagnate in the above-mentioned strong acidic atmosphere for longer than the allowable stagnation time, and as a result will rust and have to be discarded. .

そこで本発明者等は、上述の問題を解決するべく鋭意実
験検討を重ねた結果、従来使用されていたリン酸亜鉛処
理液における亜硝酸イオン含有量が0.3x 10M/
l −0,8x 10M/1であったのに対し、亜硝酸
イオン含有1が1.OX 10M /l〜2.5x 1
0’M /lとなるように亜硝酸イオンを過剰に添加し
た場合、その過剰な亜硝酸イオンはアンモニア、亜硝酸
等の窒素化合物として系外に排出され、これらの窒素化
合物はリン酸亜鉛処理槽近辺の雰囲気を中和する効果及
び被処理物たる鉄の表面に軽度の不導体被膜を形成する
効果が期待でき、それらの効果によりリン酸亜鉛処理槽
近辺に停滞する被処理物の発錆を防止することができる
ことを見出し、この発明をなすに至ったのである。
Therefore, the present inventors conducted intensive experimental studies to solve the above-mentioned problem, and found that the nitrite ion content in the conventionally used zinc phosphate treatment solution was 0.3x 10M/
l -0.8x 10M/1, while 1 containing nitrite ions was 1. OX 10M/l~2.5x 1
When nitrite ions are added in excess to 0'M/l, the excess nitrite ions are discharged from the system as nitrogen compounds such as ammonia and nitrous acid, and these nitrogen compounds are treated with zinc phosphate. It can be expected to have the effect of neutralizing the atmosphere around the tank and forming a light nonconducting film on the surface of the iron to be treated, and these effects will prevent the rusting of the to-be-treated materials stagnant near the zinc phosphate treatment tank. They discovered that it is possible to prevent this, and have come up with this invention.

すなわち、この発明は、リン酸亜鉛処理被処理物がリン
酸亜鉛処理槽近辺において停滞しても発錆しないように
することにより、被処理物が停滞することが可能な時間
を長くして塗装下地処理工程をそ、の前後の機械加工・
組付工程及び塗装工程と共に一連の連続工程とすること
を可能にし、もって生産性の向上、生産スペースの縮小
を図ると共に、またコンベアトラブルの際の被処理物廃
棄数を減少させ生産コストの低減を図ることを目的とす
るものであって、リン酸亜鉛処理液に被処理物を浸漬し
て、被処理物表面にリンm塩被膜を形成する塗装下地処
理方法において、上記リン酸亜鉛処理液中の亜硝酸イオ
ン添加量を1.OX 10 M/β以上2.5X lσ
3M / 1 以下としたことを特徴とする塗装下地処
理方法を要旨とするものである。
In other words, the present invention prevents the zinc phosphate treatment object from rusting even if it stagnates near the zinc phosphate treatment tank, thereby increasing the time during which the object can stagnate and painting. Machining and machining before and after the surface treatment process
This makes it possible to perform a series of continuous processes together with the assembly process and painting process, thereby improving productivity and reducing production space, as well as reducing the number of discarded materials in the event of conveyor trouble, reducing production costs. In a painting base treatment method in which a workpiece is immersed in a zinc phosphate treatment solution to form a phosphorous salt film on the surface of the workpiece, the above-mentioned zinc phosphate treatment solution is used. The amount of nitrite ion added in the inside was 1. OX 10 M/β or more 2.5X lσ
The gist of the present invention is a method for treating a base for painting, which is characterized in that it is 3M/1 or less.

以下にこの発明の方法をさらに詳細に説明する。The method of the present invention will be explained in more detail below.

第1図は、リン酸亜鉛処理液を貯留したリン酸亜鉛処理
槽1およびその近辺を示す。図に示されるように、この
リン酸亜鉛処理槽1にはリン酸亜鉛処理液2が貯留され
ており、このリン酸亜鉛処理液2には亜硝酸イオンが過
剰に添加されている。
FIG. 1 shows a zinc phosphate treatment tank 1 storing a zinc phosphate treatment solution and its vicinity. As shown in the figure, a zinc phosphate treatment solution 2 is stored in this zinc phosphate treatment tank 1, and nitrite ions are added in excess to this zinc phosphate treatment solution 2.

図示されるように、かかるリン酸亜鉛処理槽1のリン酸
亜鉛処理液2に対して、被処理物3が浸漬され、塗装下
地処理が施される。而して、リン酸亜鉛処理液2には、
前述したように、過剰な亜硝酸イオンが含まれることか
ら、その過剰な亜硝酸イオンがアンモニア、硝酸等の窒
素化合物として、リン酸亜鉛処理槽1近辺の雰囲気中に
排出される。
As shown in the figure, the object to be treated 3 is immersed in the zinc phosphate treatment solution 2 in the zinc phosphate treatment tank 1, and a base treatment for painting is performed. Therefore, the zinc phosphate treatment solution 2 contains
As described above, since excess nitrite ions are contained, the excess nitrite ions are discharged into the atmosphere around the zinc phosphate treatment tank 1 as nitrogen compounds such as ammonia and nitric acid.

そして、その排出窒素化合物によりリン酸亜鉛処理槽1
の前方部分近辺4及び後方部分近辺5の強酸性雰囲気が
中和される。また、同時に、そのすン酸亜鉛処理槽1の
前方部分近辺4若しくは後方部分近辺5に停滞する被処
理物3の表面には軽度の不働態被膜が形成される。その
結果、リン酸亜鉛処理槽1近辺に停滞する被処理物3の
発錆は防止される。
The discharged nitrogen compounds are then used in the zinc phosphate treatment tank 1.
The strongly acidic atmosphere near the front portion 4 and the rear portion 5 of is neutralized. At the same time, a light passive film is formed on the surface of the object to be treated 3 that remains near the front portion 4 or the rear portion 5 of the zinc sulfate treatment tank 1. As a result, the object to be treated 3 stagnant in the vicinity of the zinc phosphate treatment tank 1 is prevented from rusting.

上述の場合において、リン酸亜鉛処理液2に対して亜硝
酸イオンを2.5x 10 M、/ 1以上添加した場
合には、リン酸亜鉛処理槽1近辺に対する有害成分の排
出が多くなり、安全衛生上好ましくない。また、亜硝酸
イオンの添加量が1.OX 10 M/1未満である場
合には、リン酸亜鉛処理槽1近辺の強酸性雰囲気に対す
る中和効果が期待できない。したがって、リン酸曲鉛処
理液2に対する亜硝酸イオンの添加量は1.Ox10M
/1以上2.5×10M/1以下にすることが必要であ
る。なお、このように亜硝酸イオンを過剰に添加する場
合に、リン酸亜鉛処理液2の成分として塩素酸イオンが
含まれていると、窒素化合物の排出と共に塩素も排出さ
れ、防錆効果が著しく低下する。したがってこの発明の
方法に使用されるリン酸亜鉛処理液成分としては塩素酸
イオンを含まないものを用いる。その他の成分は、従来
のリン酸亜鉛処理液と同様であれば良く、したがって通
常はリン酸イオオン28.Ox10M/1〜5.5X 
16M/1 、硝酸とすれば良い。
In the above case, if nitrite ions are added to the zinc phosphate treatment solution 2 at a rate of 2.5x 10 M,/1 or more, harmful components will be discharged to the vicinity of the zinc phosphate treatment tank 1, resulting in safety concerns. Not sanitary. Also, the amount of nitrite ion added is 1. If it is less than OX 10 M/1, a neutralizing effect on the strong acid atmosphere near the zinc phosphate treatment tank 1 cannot be expected. Therefore, the amount of nitrite ions added to the curved lead phosphate treatment solution 2 is 1. Ox10M
/1 or more and 2.5×10M/1 or less. In addition, when adding nitrite ions in excess in this way, if chlorate ions are included as a component of the zinc phosphate treatment solution 2, chlorine is also discharged along with nitrogen compounds, and the rust prevention effect is significantly reduced. descend. Therefore, the zinc phosphate treatment solution components used in the method of the present invention do not contain chlorate ions. The other components may be the same as those in conventional zinc phosphate treatment solutions, and therefore usually include phosphate ions. Ox10M/1~5.5X
16M/1, nitric acid may be used.

次に、この発明の実施例を下表を参照して説明する。用
いられたリン酸亜鉛処理液は日本バー力ライジング(株
)製のBt137B(商品名)であり、その基本成分は
、リン酸イオンが1.2X i7 OM/1、亜鉛イオンが3.Ox 10M/1 、硝酸
イオンが2.5x 10M/ 1 、であり、さらにこ
の基本成分に対する亜硝酸イオンの添加量を0.3×1
0M/f 、  0.5X 10M/1.1.OX10
M/11 、 2.Ox 10M/l 、  3.Ox
 10M/1と5段階に変化させた。またリン酸亜鉛処
理液の温度は50℃とした。そして、そのリン酸亜鉛処
理液の雰囲気中に被処理物を停滞させる時間を、3分、
30分、60分と変化させて、被処理物の表面状態を調
べた。なお、表中、Q印は被処理物表面状態が良好な場
合、Δ印は被処理物表面にやや錆が発生している場合、
x印は被処理物表面に明らかに錆が発生している場合で
ある。
Next, examples of the present invention will be described with reference to the table below. The zinc phosphate treatment solution used was Bt137B (trade name) manufactured by Nihon Bariki Rising Co., Ltd., and its basic components were phosphate ions at 1.2X i7 OM/1 and zinc ions at 3. Ox 10M/1, nitrate ion is 2.5x 10M/1, and the amount of nitrite ion added to this basic component is 0.3x1.
0M/f, 0.5X 10M/1.1. OX10
M/11, 2. Ox 10M/l, 3. Ox
It was changed in 5 steps to 10M/1. Further, the temperature of the zinc phosphate treatment solution was 50°C. Then, the time for which the object to be treated is stagnant in the atmosphere of the zinc phosphate treatment solution is set to 3 minutes.
The surface condition of the object to be treated was examined after changing the time to 30 minutes and 60 minutes. In addition, in the table, mark Q indicates that the surface condition of the object to be treated is good, mark Δ indicates that the surface of the object to be treated is slightly rusted,
An x mark indicates a case where rust is clearly generated on the surface of the object to be treated.

この表に示されるように、亜硝酸イオンの量が1.0×
10M/I1以上の場合、被処理物がリン酸亜鉛処理液
雰囲気中に1時間停滞しても発錆はみられなかった。
As shown in this table, the amount of nitrite ion is 1.0×
In the case of 10M/I1 or more, no rust was observed even if the object to be treated stagnated in the zinc phosphate treatment solution atmosphere for one hour.

更に、他の実施例として、上記実施例と同じ処理条件に
より、硝酸イオン添加量を1.sX 10 M/1に設
定して、第1図に示される装置を用いて、被処理物3を
リン酸亜鉛処理槽1の前方部分近辺4及び後方部分近辺
5及びリン酸亜鉛処理W11内に実際に停滞させたとき
の発錆状況を試験したところ、どの被処理物3も停滞後
2時間まで錆の発生はみられなかった。
Furthermore, as another example, the amount of nitrate ion added was changed to 1. sX 10 M/1, and using the apparatus shown in FIG. When the rusting conditions were actually tested when the objects were stagnated, no rust was observed in any of the objects 3 until 2 hours after the objects 3 had been stagnated.

以上のようにこの発明によれば、塗装下地処理を行なう
リン酸亜鉛処理液に過剰な亜硝酸イオンを添加し、当該
リン酸亜鉛処理液から排出される窒素化合物によってリ
ン酸亜鉛処理槽近辺の雰囲気を中和し、同時にリン酸亜
鉛処理槽近辺において停滞する被処理物の表面に軽度の
不働態被膜を形成して、停滞する被処理物の発錆を長時
間にわたり防止するようにしたので、リン酸亜鉛処理槽
近辺において被処理物が停滞し得る時間が非常に長く□
なり、その結果、塗装下地処理工程を、その前後の機械
加工・組付工程及び、塗装工程と共に一連の連続工程と
することが可能となり、生産性の向上や生産スペースの
縮小を図ることができる。
As described above, according to the present invention, excessive nitrite ions are added to the zinc phosphate treatment solution for treating the base for painting, and the nitrogen compounds discharged from the zinc phosphate treatment solution cause damage to the vicinity of the zinc phosphate treatment tank. It neutralizes the atmosphere and at the same time forms a light passive film on the surface of the stagnant workpiece near the zinc phosphate treatment tank, preventing rusting of the stagnant workpiece for a long time. , the amount of time the material to be treated can stagnate near the zinc phosphate treatment tank is extremely long□
As a result, it becomes possible to perform the painting base treatment process as a series of continuous processes together with the machining/assembly process before and after it, and the painting process, making it possible to improve productivity and reduce production space. .

また、長時間にわたり復旧しないコンベアトラブルが発
生しても、被処理物の発錆を長時間にわたり防止するこ
とができ、被処理物廃棄数を減少させて、生産コストの
低減を図ることができる。
In addition, even if a conveyor problem occurs that does not recover for a long time, it is possible to prevent the objects to be processed from rusting for a long time, reducing the number of objects to be discarded and reducing production costs. .

【図面の簡単な説明】[Brief explanation of the drawing]

第1図はこの発明を実施する際に用いるリン酸亜鉛処理
槽の断面図である。 1・・・リン酸亜鉛処理槽、 2・・・リン酸亜鉛処理
液、3・・・被処理物。 出願人  トヨタ自動車株式会社 代理人  弁理士 豊 1)武 久 (ほか1名) 第1図
FIG. 1 is a sectional view of a zinc phosphate treatment tank used in carrying out the present invention. 1... Zinc phosphate treatment tank, 2... Zinc phosphate treatment liquid, 3... Treated object. Applicant Toyota Motor Corporation Agent Patent Attorney Yutaka 1) Hisashi Take (and 1 other person) Figure 1

Claims (1)

【特許請求の範囲】[Claims] リン酸亜鉛処理液に被処理物を浸漬して、被処理物表面
にリン酸塩被膜を形成する塗装下地処理方法において、
上記リン酸亜鉛処理液中の亜硝酸イオン添加量を1.O
x10M/1以上2.5X 10M/l以下としたこと
を特徴とする塗装下地処理方法。
In a painting base treatment method in which a treated object is immersed in a zinc phosphate treatment solution to form a phosphate film on the surface of the treated object,
The amount of nitrite ions added in the above zinc phosphate treatment solution was 1. O
A method for treating a base for painting, characterized in that the treatment is at least x10M/l and at most 2.5 x 10M/l.
JP4759383A 1983-03-22 1983-03-22 Method for treating substrate of painting Pending JPS59173167A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4759383A JPS59173167A (en) 1983-03-22 1983-03-22 Method for treating substrate of painting

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4759383A JPS59173167A (en) 1983-03-22 1983-03-22 Method for treating substrate of painting

Publications (1)

Publication Number Publication Date
JPS59173167A true JPS59173167A (en) 1984-10-01

Family

ID=12779542

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4759383A Pending JPS59173167A (en) 1983-03-22 1983-03-22 Method for treating substrate of painting

Country Status (1)

Country Link
JP (1) JPS59173167A (en)

Similar Documents

Publication Publication Date Title
EP0689620B1 (en) Non-chrome passivation for metal substrates
CA1200739A (en) Process for phosphating metal surfaces
EP0312176B1 (en) Process for applying conversion coatings
EP0106459A1 (en) Phosphate coating metal surfaces
JPS5811514B2 (en) How to protect metal surfaces
JPH04228579A (en) Method for treating metal surface with phosphate
US4595424A (en) Method of forming phosphate coating on zinc
DE3689442T2 (en) Acidic, aqueous phosphate coating solutions for a process for phosphate coating of metallic surfaces.
US4600447A (en) After-passivation of phosphated metal surfaces
JP3325366B2 (en) Chemical conversion treatment liquid composition for magnesium-containing metal, chemical conversion treatment method, and chemical conversion-treated material
CA1224121A (en) Process for phosphating metals
US2702768A (en) Ferrous surface coating process using alkali metal phosphates and hydroxylamines
KR20020077150A (en) Chemical conversion reagent for magnesium alloy, surface treating method, and magnesium alloy substrate
GB2158845A (en) Composition and process for treatment of ferrous substrates
JPH02190478A (en) Formation of phosphate film
US20040094235A1 (en) Chrome free treatment for aluminum
US5383982A (en) Process of producing phosphate coatings
CA1098427A (en) Process of phosphating an iron substrate
US3493440A (en) Method for phosphate coating ferrous metal surfaces and finishing treatment thereof
SI20378A (en) Aqueous solution and method for phosphatizing metallic surfaces
JPS59173167A (en) Method for treating substrate of painting
EP0061911A1 (en) Process and composition for treating phosphated metal surfaces
JPH02101174A (en) Treatment with zinc phosphate for cold working
US2795518A (en) Process for treating steel, zinc, and aluminum to increase corrosion resistance
KR102076905B1 (en) Composition of post treatment agent for metal surface treatment