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JPH07100872B2 - Chemical conversion treatment liquid for aluminum and aluminum alloys - Google Patents

Chemical conversion treatment liquid for aluminum and aluminum alloys

Info

Publication number
JPH07100872B2
JPH07100872B2 JP2040168A JP4016890A JPH07100872B2 JP H07100872 B2 JPH07100872 B2 JP H07100872B2 JP 2040168 A JP2040168 A JP 2040168A JP 4016890 A JP4016890 A JP 4016890A JP H07100872 B2 JPH07100872 B2 JP H07100872B2
Authority
JP
Japan
Prior art keywords
chemical conversion
treatment liquid
aluminum
conversion treatment
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 - Lifetime
Application number
JP2040168A
Other languages
Japanese (ja)
Other versions
JPH03243781A (en
Inventor
昌之 ▲吉▼田
和也 中田
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.)
Nihon Parkerizing Co Ltd
Original Assignee
Nihon Parkerizing 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 Nihon Parkerizing Co Ltd filed Critical Nihon Parkerizing Co Ltd
Priority to JP2040168A priority Critical patent/JPH07100872B2/en
Priority to DE69103139T priority patent/DE69103139T2/en
Priority to AU73370/91A priority patent/AU642478B2/en
Priority to PCT/US1991/000965 priority patent/WO1991013186A1/en
Priority to BR919106049A priority patent/BR9106049A/en
Priority to US07/923,889 priority patent/US5451271A/en
Priority to CA 2072592 priority patent/CA2072592A1/en
Priority to EP91904950A priority patent/EP0516700B1/en
Publication of JPH03243781A publication Critical patent/JPH03243781A/en
Publication of JPH07100872B2 publication Critical patent/JPH07100872B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明はアルミニウムおよびアルミニウム合金を塗装す
る前に、該表面に優れた耐食性と塗料密着性を付与する
新規なアルミニウムおよびアルミニウム合金の化成処理
液に関し、例えば、飲料缶の蓋材すなわち缶エンド材等
の表面に効果的に適用されるものである。
DETAILED DESCRIPTION OF THE INVENTION [Industrial field of application] The present invention relates to a novel aluminum and aluminum alloy chemical conversion treatment liquid which imparts excellent corrosion resistance and paint adhesion to the surface of aluminum and aluminum alloy before coating. With regard to this, for example, it is effectively applied to the surface of a lid material of a beverage can, that is, a can end material.

〔従来の技術〕 アルミニウムおよびアルミニウム合金の化成処理液とし
てはクロメートタイプとノンクロメートタイプに大別で
きる。クロメートタイプの代表的なものとしては、クロ
ム酸クロメート処理とりん酸クロメート処理とがあり、
クロム酸クロメート処理は1950年頃に実用化され現在も
熱交換器のフィン材などに広く使用されている。化成処
理液はクロム酸(CrO3)とフッ化水素酸(HF)が主成分
でさらに促進剤が添加されているものであって、若干6
価クロムを含有する皮膜を形成する。りん酸クロメート
化成処理は米国特許第2,438,877号明細書に開示されて
おり、化成処理液はクロム酸(CrO3)、りん酸(H3P
O4)、フッ化水素酸(HF)からなり、形成される皮膜は
水和したりん酸クロム(CrPO4・4H2O)を主成分とする
ものである。この皮膜は6価クロムを含有しないことか
ら、飲料用缶および蓋材の塗装下地処理として現在も広
く使用されている。
[Prior Art] Chemical conversion treatment liquids for aluminum and aluminum alloys can be roughly classified into chromate type and non-chromate type. Typical chromate types are chromate chromate treatment and phosphoric acid chromate treatment,
Chromate chromate treatment was put into practical use around 1950 and is still widely used for fin materials for heat exchangers. The chemical conversion treatment liquid contains chromic acid (CrO 3 ) and hydrofluoric acid (HF) as main components, and further contains an accelerator.
A film containing valent chromium is formed. Phosphoric acid chromate chemical conversion treatment is disclosed in US Pat. No. 2,438,877, and the chemical conversion treatment liquid is chromic acid (CrO 3 ) or phosphoric acid (H 3 P
O 4 ), hydrofluoric acid (HF), and the film formed is mainly composed of hydrated chromium phosphate (CrPO 4 .4H 2 O). Since this coating does not contain hexavalent chromium, it is still widely used as a coating base treatment for beverage cans and lid materials.

以上説明したクロメートタイプの処理液とは別にノンク
ロメートタイプのものが開発されており、その代表的な
発明として特開昭52−131937号公報に開示されたものが
挙げられる。この開示された処理液は、ジルコニウムま
たはチタンあるいはこれらの混合物、ホスフェートおよ
びフッ化物を含有し、且つ、pHが約1.0〜4.0の酸性の水
性コーティング溶液である。この開示された化成処理液
を用いて処理を行うとアルミニウム表面上にジルコニウ
ムあるいはチタンの酸化物を主成分とする化成皮膜を形
成する。しかしながら、ノンクロメートタイプの処理液
は6価クロムを含有しないという利点を有するもののク
ロムメートタイプに比べると耐食性および塗料密着性が
劣るという欠点を有しているのである。
In addition to the chromate type treatment liquid described above, a non-chromate type liquid has been developed, and a representative invention thereof is the one disclosed in JP-A-52-131937. The disclosed processing solution is an acidic aqueous coating solution containing zirconium or titanium or mixtures thereof, phosphates and fluorides and having a pH of about 1.0-4.0. When a treatment is performed using the disclosed chemical conversion treatment liquid, a chemical conversion film containing zirconium or titanium oxide as a main component is formed on the aluminum surface. However, the non-chromate type treatment liquid has the advantage that it does not contain hexavalent chromium, but has the drawback that it is inferior in corrosion resistance and paint adhesion compared to the chromate type treatment liquid.

一方、アルミニウム合金の板またはコイルは、塗装され
飲料用缶の蓋材すなわち缶エンド材として広く使用され
ているが、耐食性および塗料密着性向上のために化成処
理がなされており、国内では殆んどの場合にりん酸クロ
メート処理が採用されている。これに対してノンクロメ
ートタイプの化成処理はりん酸クロメート処理に比べ塗
料密着性が劣るために米国で一部採用されているにすぎ
ないのが現状である。缶エンド材用のりん酸クロメート
化成処理の場合は一般的に、りん酸イオン10.0〜40.0g/
l、6価クロム2.0〜4.0g/lおよびフッ素イオン0.7〜1.5
g/lを含有する処理液で処理されている。また、缶エン
ド材の塗装には現在、塩化ビニル系の塗料が主に使用さ
れている。すなわち、缶エンジはアルミニウム合金のコ
イルあるいは板材をりん酸クロメート処理し、塩化ビニ
ル系の塗料を塗布して、その後成型という工程により生
産されている。
On the other hand, aluminum alloy plates or coils are painted and widely used as lid materials for beverage cans, that is, as can end materials, but they have undergone chemical conversion treatment to improve corrosion resistance and paint adhesion, and are used in most of Japan. In all cases, chromate phosphate treatment is used. In contrast, the non-chromate type chemical conversion treatment is inferior to the phosphoric acid chromate treatment in paint adhesion, and is currently only partially used in the United States. In the case of phosphoric acid chromate chemical conversion treatment for can end materials, phosphate ion is generally 10.0 to 40.0 g /
l, hexavalent chromium 2.0-4.0g / l and fluorine ion 0.7-1.5
It is treated with a treatment solution containing g / l. At present, vinyl chloride-based paints are mainly used for painting can end materials. That is, the can engineer is produced by a process in which an aluminum alloy coil or plate material is chromated with phosphoric acid, a vinyl chloride-based paint is applied, and then molding is performed.

〔発明が解決しようとする課題〕[Problems to be Solved by the Invention]

前記従来例で処理されたアルミニウム合金またはコイル
を用いて成形された缶エンドと、ジュースやビールなど
が充填された缶本体により飲料用缶が形成された飲料用
缶は、その充填物によりパック後に相当過酷な条件で殺
菌処理されるのである。この殺菌工程において、水蒸気
は塗膜を透過し、透過した水蒸気はその後塗膜と化成皮
膜との界面で凝縮し、これにより塗膜の密着力が低下す
るといった問題が発生しやすいのである。実際に、缶エ
ンドの一部がイージーオープン方式で開缶された時に、
開孔部に塗膜剥離による欠陥(エナメルフェザー)を生
じることがあるので、この対応として塗料密着性の向上
は従来例において解決しなければならない重要な課題で
ある。
The can end formed by using the aluminum alloy or coil treated in the conventional example, and the beverage can in which the beverage can is formed by the can main body filled with juice, beer, etc., is packed after the packing. It is sterilized under considerably severe conditions. In this sterilization step, water vapor permeates the coating film, and the permeated water vapor then condenses at the interface between the coating film and the chemical conversion film, which tends to cause a problem that the adhesion of the coating film is reduced. In fact, when a part of the can end is opened by the easy open method,
Since a defect (enamel feather) due to the peeling of the coating film may occur in the opening portion, the improvement of the coating adhesion is an important issue to be solved in the conventional example as a countermeasure.

〔課題を解決するための手段〕[Means for Solving the Problems]

前記従来例の課題を解決する具体的手段として本発明
は、りん酸イオン5.0〜40.0g/l、6価クロムイオン1.0
〜4.0g/lおよびフッ素イオン0.1〜2.0g/l、フルオロケ
イ酸イオンを4.0〜15.0g/lもしくはフルオロホウ酸イオ
ンを0.5〜3.0g/lを含有し、pHを1.0〜3.0にしたことを
特徴とするアルミニウムおよびアルミニウム合金用化成
処理液を提供するものであり、該化成処理液によってア
ルミニウムあるいはアルミニウム合金表面に優れた耐食
性を付与し、且つ塗料密着性の非常に優れた化成皮膜を
形成することができるのである。つまり、アルミニウム
およびアルミニウム合金を塗装する前に、その表面に優
れた耐食性と塗料密着性とを付与する化成処理液を提供
しようとするものである。
As a concrete means for solving the above-mentioned problems of the conventional example, the present invention provides a phosphate ion of 5.0 to 40.0 g / l and a hexavalent chromium ion of 1.0.
~ 4.0 g / l and fluoride ion 0.1 ~ 2.0 g / l, fluorosilicate ion 4.0 ~ 15.0 g / l or fluoroborate ion containing 0.5 ~ 3.0 g / l, pH to 1.0 ~ 3.0 The present invention provides a chemical conversion treatment liquid for aluminum and aluminum alloys, which imparts excellent corrosion resistance to the surface of aluminum or an aluminum alloy by the chemical conversion treatment liquid and forms a chemical conversion film having excellent paint adhesion. It is possible. That is, it is intended to provide a chemical conversion treatment liquid which imparts excellent corrosion resistance and paint adhesion to the surface of aluminum and aluminum alloy before coating.

〔組成および処理工程の説明〕[Description of composition and processing steps]

本発明の化成処理液はフッ素錯体イオン、りん酸イオ
ン、6価クロム、フッ素イオンを必須成分として含む酸
性処理液に関するものである。
The chemical conversion treatment liquid of the present invention relates to an acidic treatment liquid containing fluorine complex ions, phosphate ions, hexavalent chromium and fluorine ions as essential components.

フッ素錯体イオンはフルオロケイ酸イオンとフルオロホ
ウ酸イオンから選択される。フッ素錯体イオンの含有に
はフルオロケイ酸、フルオロホウ酸およびこの可溶性塩
から任意に選んで使用できる。フルオロケイ酸イオンの
場合には4.0〜15.0g/lの範囲が好ましく、4.0g/l未満で
は良好な塗料密着性が限られない。逆に15.0g/lを超え
るとエッチングが多くなり皮膜が充分に形成されない。
フルオロホウ酸イオンの場合には0.5〜3.0g/lの範囲が
好ましく、0.5g/l未満の場合には良好な塗料密着性が得
られない。逆に3.0g/lを超えると廃水処理性が悪くなり
経済上の問題がある。
The fluorine complex ion is selected from fluorosilicate ion and fluoroborate ion. Fluorosilicic acid, fluoroboric acid and soluble salts thereof can be arbitrarily selected and used for containing the fluorine complex ion. In the case of fluorosilicate ion, the range of 4.0 to 15.0 g / l is preferable, and if it is less than 4.0 g / l, good paint adhesion is not limited. On the other hand, if it exceeds 15.0 g / l, etching will increase and the film will not be formed sufficiently.
In the case of fluoroborate ion, the range of 0.5 to 3.0 g / l is preferable, and if it is less than 0.5 g / l, good paint adhesion cannot be obtained. On the other hand, if it exceeds 3.0 g / l, the wastewater treatment becomes poor and there is an economic problem.

りん酸イオンを含有させるにはりん酸(H3PO4)を使用
することが好ましい。りん酸の含有量は5.0〜40.0g/lの
範囲が好ましく、5.0g/l未満では形成される皮膜にりん
酸クロムが少なくなり塗料密着性が低下する。40.0g/l
を超えても良好な皮膜は形成されるが、処理液のコスト
が高くなり経済的に問題がある。
It is preferable to use phosphoric acid (H 3 PO 4 ) to contain phosphate ions. The content of phosphoric acid is preferably in the range of 5.0 to 40.0 g / l, and if it is less than 5.0 g / l, the amount of chromium phosphate in the formed film will be small and the coating adhesion will be poor. 40.0g / l
Even if it exceeds the above range, a good film is formed, but the cost of the treatment liquid becomes high, which is economically problematic.

6価クロムを含有させるにはクロム酸(CrO3)を使用す
ることが好ましい。このクロム酸の含有量は6価クロム
イオンとして1.0〜4.0g/lの範囲が好ましく1g/l未満で
は化成皮膜が充分に形成されないため耐食性が劣る。4.
0g/lを超えると処理液の廃水処理性が悪くなり、環境上
及び経済上の問題がある。
Chromic acid (CrO 3 ) is preferably used to contain hexavalent chromium. The content of chromic acid is preferably in the range of 1.0 to 4.0 g / l as hexavalent chromium ions, and if it is less than 1 g / l, the chemical conversion film is not sufficiently formed and the corrosion resistance is poor. Four.
If it exceeds 0 g / l, the treatment of wastewater of the treatment liquid becomes poor, and there are environmental and economic problems.

フッ素イオンは化成皮膜の皮膜成長速度を左右する重要
成分である。フッ素イオンを含有させるにはフッ化水素
酸(HF)、フッ化ナトリウム(NaF)、フッ化カリウム
(KF)などを使用することができる。化成液中のフッ素
イオン濃度は以下の如く規定した。イオン電極(フッ素
F-125、比較HS-305DP東亜電波工業(株)製)およびイ
オンメーター(IM-40S東亜電波工業(株)製)を用い、
クロム酸5g/l、リン酸15g/lにフッ化水素酸を一定量
(例えば0.1g/l、1g/l、10g/l)を加え、リン酸あるい
は水酸化ナトリウムでpHを2.0に調整した液を基準液
(フッ素イオン濃度は添加したフッ化水素酸の全フッ素
量と規定)とし校正した。そして、化成液のpHをリン酸
あるいは水酸化ナトリウムで2.0に調整後、フッ素イオ
ンメーターで測定し、その測定値をフッ素イオン濃度と
した。
Fluoride ion is an important component that affects the film growth rate of the chemical conversion film. Hydrofluoric acid (HF), sodium fluoride (NaF), potassium fluoride (KF) and the like can be used to contain the fluoride ion. The fluorine ion concentration in the chemical conversion liquid was defined as follows. Ion electrode (fluorine
Using F-125, comparative HS-305DP Toa Denpa Kogyo KK and ion meter (IM-40S Toa Denpa Kogyo KK)
Chromic acid 5 g / l, phosphoric acid 15 g / l, and fixed amount of hydrofluoric acid (for example, 0.1 g / l, 1 g / l, 10 g / l) were adjusted to pH 2.0 with phosphoric acid or sodium hydroxide. The solution was used as a standard solution (fluoride ion concentration was defined as the total amount of fluorine in the added hydrofluoric acid) and calibrated. Then, the pH of the chemical conversion liquid was adjusted to 2.0 with phosphoric acid or sodium hydroxide and then measured with a fluorine ion meter, and the measured value was defined as the fluorine ion concentration.

このフッ素イオンの濃度は0.1〜2.0g/lの範囲が好まし
く、0.1g/l未満では成長速度が遅すぎ、充分な化成皮膜
を得るには長時間処理を行わなければならず生産性が劣
るという問題がある。逆に2.0g/lを越えると成長速度が
速くなり、皮膜量が多くなって、不透明な外観になると
いう問題がある。したがって、濃度は0.1〜2.0g/lの範
囲が好ましく、特に0.4〜1.0g/lの範囲が好ましい。
The concentration of this fluorine ion is preferably in the range of 0.1 to 2.0 g / l, and if it is less than 0.1 g / l, the growth rate is too slow, and long-term treatment must be performed to obtain a sufficient chemical conversion film, resulting in poor productivity. There is a problem. On the contrary, if it exceeds 2.0 g / l, there is a problem that the growth rate becomes fast, the amount of film increases, and the appearance becomes opaque. Therefore, the concentration is preferably 0.1 to 2.0 g / l, particularly 0.4 to 1.0 g / l.

化成処理液のpHは1.0〜3.0の範囲に制御されるが、pHの
調整にはりん酸、硝酸、塩酸などの酸または水酸化ナト
リウム、水酸化アンモニウムなどから任意に選んで用い
ることができる。pHが1.0未満ではエッチングが多くな
って皮膜が形成され難くなり、逆にpHが3.0を超えると
エッチングが弱くなり均一な皮膜が形成できなくなる。
The pH of the chemical conversion treatment liquid is controlled in the range of 1.0 to 3.0, and an acid such as phosphoric acid, nitric acid or hydrochloric acid or sodium hydroxide, ammonium hydroxide or the like can be arbitrarily selected and used for adjusting the pH. If the pH is less than 1.0, etching will increase and it will be difficult to form a film. Conversely, if the pH exceeds 3.0, etching will be weak and a uniform film cannot be formed.

次に本発明の化成処理液による処理工程について説明す
る。本発明の化成処理液は現在広く使用されているりん
酸クロメート処理液の代替として用することが可能であ
る。アルミニウムおよびアルミニウム合金の表面に本発
明の化成処理液により化成処理を施す場合に先ず表面の
清浄化が必要であり、そのための洗浄方法としては酸
系、アルカリ系または溶剤系の洗浄液による処理または
これらの組み合せの処理のいずれでもよい。また、必要
あればアルミニウムおよびアルミニウム合金の表面を洗
浄後さらに酸あるいはアルカリによりエッチングしても
よい。本発明液による処理方法は浸漬、スプレー処理の
いずれでもよく、処理温度と処理時間は形成する化成皮
膜量を左右する因子となる。処理液の温度は室温〜70℃
の範囲が可能であり、好ましくは35〜55℃の範囲であ
り、また、処理時間は1〜90秒の範囲が好ましい。化成
皮膜量はりん酸クロメート皮膜と同様にクロム付着量で
評価する。クロム付着量は5〜50mg/m2の範囲が好まし
く、要求される耐食性の度合により調整する。クロム付
着量のコントロールは上記処理温度と処理時間を適宜調
整することにより可能である。
Next, a treatment process using the chemical conversion treatment liquid of the present invention will be described. The chemical conversion treatment liquid of the present invention can be used as a substitute for the chromate phosphate treatment liquid which is widely used at present. When the chemical conversion treatment of the present invention is performed on the surfaces of aluminum and aluminum alloys, the surface must first be cleaned, and as a cleaning method therefor, a treatment with an acid-based, alkali-based or solvent-based cleaning liquid or these Any combination of the above may be used. If necessary, the surfaces of aluminum and aluminum alloy may be washed and then further etched with acid or alkali. The treatment method using the liquid of the present invention may be either dipping or spraying, and the treatment temperature and the treatment time are factors that influence the amount of the chemical conversion film formed. The temperature of the processing solution is room temperature to 70 ℃
The range is from 35 to 55 ° C., and the treatment time is preferably from 1 to 90 seconds. The amount of the chemical conversion film is evaluated by the amount of chromium deposited as in the case of the chromate phosphate film. The amount of chromium deposited is preferably in the range of 5 to 50 mg / m 2 , and is adjusted according to the degree of corrosion resistance required. The amount of chromium deposited can be controlled by appropriately adjusting the treatment temperature and the treatment time.

本発明の化成処理液より形成される化成皮膜はりん酸ク
ロメート処理において形成される皮膜と同等であり、化
成皮膜は主に水和したりりん酸クロム(CrPO4・4H2O)
からなる。
The chemical conversion film formed from the chemical conversion treatment liquid of the present invention is equivalent to the film formed in the phosphoric acid chromate treatment, and the chemical conversion film is mainly hydrated or chromium phosphate (CrPO 4 .4H 2 O)
Consists of.

〔実施例〕〔Example〕

以下に本発明の化成処理液に関し、いくつかの実施例を
挙げ、その有用性を比較例と対比して表1に示す。
Several examples of the chemical conversion treatment liquid of the present invention will be given below, and their usefulness is shown in Table 1 in comparison with comparative examples.

素材には、アルミニウム−マグネシウム合金(JIS A508
2)を使用した。このアルミニウム合金の脱脂および化
成処理には小型スプレー装置を使用した。この小型スプ
レー装置は、現在、アルミニウム合金のコイルの化成処
理において使用されている連続化成処理ラインにおいて
スプレー処理された場合と同様のスプレー条件になるよ
う設計されている。化成処理されたアルミニウム合金板
に缶エンド用塗料(塩化ビニル系)を塗膜厚12〜14μm
に塗装し、200℃で10分間焼付けを行い試験板とした。
また、化成皮膜のクロム付着量は蛍光X線分析装置(理
学電機工業製3070F型)を用い測定した。
The material is aluminum-magnesium alloy (JIS A508
2) was used. A small spray device was used for degreasing and chemical conversion treatment of this aluminum alloy. This small-sized spray device is designed to have the same spraying conditions as when sprayed in the continuous chemical conversion treatment line currently used in the chemical conversion treatment of the aluminum alloy coil. Painted for can ends (vinyl chloride type) on chemical-treated aluminum alloy sheets, coating thickness 12-14 μm
It was painted on and baked at 200 ° C for 10 minutes to obtain a test plate.
Further, the amount of chromium deposited on the chemical conversion film was measured using a fluorescent X-ray analyzer (Rigaku Denki Kogyo Model 3070F).

耐食性の評価には塩水噴霧試験を行った。塩水噴霧試験
は、JIS2-2371に準拠し塗装後の試験板の塗膜クロスカ
ット部のフクレ発生までの時間で表記した。したがっ
て、時間が長いほど耐食性は優れる。噴霧時間が2000時
間以上であれば良好である。塗料密着性は塗装後の試験
板を5×150mmの短冊状に切断し、ポリアミド系のフィ
ルムで熱圧着し試片とし、これを脱イオン沸水に3時間
浸漬後180度ピール試験法により剥離し、その際のピー
ル強度より評価した。したがって、ピール強度が大きい
ほど塗料密着性は優れる。一般に3.0kgf/5mm幅であれば
良好である。また、エナメルフェザーの評価には、軽金
属学会第73回秋期大会講演概要(p49)に記載のアルコ
ア法に準拠し行った。評価は剥離後の最大塗膜残存幅で
行った。したがって、塗膜残存幅が小さいほどエナメル
フェザーに優れる。一般に残存幅が0.5mm以下であれば
良好である。
A salt spray test was conducted to evaluate the corrosion resistance. The salt spray test is based on JIS 2-2371 and is expressed as the time until blistering occurs in the coating film cross-cut portion of the test plate after coating. Therefore, the longer the time, the better the corrosion resistance. It is good if the spraying time is 2000 hours or more. For paint adhesion, the test plate after coating is cut into 5 x 150 mm strips and thermocompression bonded with a polyamide film to form a test piece, which is immersed in deionized boiling water for 3 hours and then peeled off by the 180 degree peel test method. Then, the peel strength at that time was evaluated. Therefore, the greater the peel strength, the better the paint adhesion. Generally, a width of 3.0 kgf / 5 mm is good. The enamel feather was evaluated according to the Alcoa method described in the lecture summary of the 73rd Autumn Meeting of the Japan Institute of Light Metals (p49). The evaluation was performed with the maximum width of the remaining coating film after peeling. Therefore, the smaller the remaining width of the coating film, the better the enamel feather. Generally, it is good if the residual width is 0.5 mm or less.

実施例1 アルミニウム合金を市販の強アルカリ性脱脂剤(登録商
標ファインクリーナー4418、日本パーカライジング株式
会社製)の4%加熱水溶液(70℃)を用いて洗浄し、次
いで水洗し表面を清浄にした後、化成処理液1を50℃に
加温して5秒間スプレー処理し次いで水道水で水洗し、
さらに3000,000Ωcm以上の脱イオン水で10秒間スプレー
した後、70℃の熱風乾燥炉内で5分間乾燥した。乾燥
後、前記の条件で塗装を行い耐食性、塗料密着性、エナ
メルフェザーを評価した。
Example 1 An aluminum alloy was washed with a 4% heated aqueous solution (70 ° C.) of a commercially available strong alkaline degreasing agent (registered trademark Fine Cleaner 4418, manufactured by Nippon Parkerizing Co., Ltd.), and then washed with water to clean the surface, Chemical conversion treatment liquid 1 is heated to 50 ° C., sprayed for 5 seconds, then washed with tap water,
After further spraying with deionized water of 3,000,000 Ωcm or more for 10 seconds, it was dried in a hot air drying oven at 70 ° C for 5 minutes. After drying, coating was performed under the above conditions to evaluate corrosion resistance, paint adhesion, and enamel feather.

化成処理液1 40%フルオロケイ酸(H2SiF6) 18.8g/l(SiF6 2-7.4g/l) 75%りん酸(H3PO4) 21.3g/l(PO4 3-15.5g/l) クロム酸(CrO3) 5.8g/l(Cr6+3.0g/l) 20%フッ化水素酸(HF) 3.0g/l(F-0.6g/l) pH2.0〕水酸化アンモニウムで調整) 実施例2 実施例1と同一条件でアルミニウム合金を洗浄後、化成
処理液2を50℃に加温して5秒間スプレー処理した。処
理後、実施例1と同一条件で水洗、乾燥、塗装し、性能
を評価した。
Chemical conversion treatment liquid 1 40% fluorosilicic acid (H 2 SiF 6) 18.8g / l (SiF 6 2- 7.4g / l) 75% phosphoric acid (H 3 PO 4) 21.3g / l (PO 4 3- 15.5g / l) Chromic acid (CrO 3 ) 5.8g / l (Cr 6+ 3.0g / l) 20% Hydrofluoric acid (HF) 3.0g / l (F - 0.6g / l) pH 2.0] Ammonium hydroxide Example 2 After cleaning the aluminum alloy under the same conditions as in Example 1, the chemical conversion treatment liquid 2 was heated to 50 ° C. and sprayed for 5 seconds. After the treatment, the performance was evaluated by washing with water, drying and coating under the same conditions as in Example 1.

化成処理液2 40%フルオロケイ酸(H2SiF6) 12.5g/l(SiF6 2-4.9g/l) 75%りん酸(H3PO4) 21.3g/l(PO4 3-15.5g/l) クロム酸(CrO3) 5.8g/l(Cr6+3.0g/l) 20%フッ化水素酸(HF) 3.0g/l(F-0.6g/l) pH2.0(水酸化アンモニウムで調整) 実施例3 実施例1と同一条件でアルミニウム合金を清浄後、化成
処理液3を50℃に加温して5秒間スプレー処理した。処
理後、実施例1と同一条件で水洗、乾燥、塗装し、性能
を評価した。
Chemical conversion treatment liquid 2 40% fluorosilicic acid (H 2 SiF 6 ) 12.5g / l (SiF 6 2- 4.9g / l) 75% phosphoric acid (H 3 PO 4 ) 21.3g / l (PO 4 3- 15.5g / l) Chromic acid (CrO 3 ) 5.8g / l (Cr 6+ 3.0g / l) 20% Hydrofluoric acid (HF) 3.0g / l (F - 0.6g / l) pH 2.0 (ammonium hydroxide Example 3 After cleaning the aluminum alloy under the same conditions as in Example 1, the chemical conversion treatment liquid 3 was heated to 50 ° C. and sprayed for 5 seconds. After the treatment, the performance was evaluated by washing with water, drying and coating under the same conditions as in Example 1.

化成処理液3 40%フルオロケイ酸(H2SiF6) 18.8g/l(SiF6 2-7.4g/l) 75%りん酸(H3PO4) 21.3g/l(PO4 3-15.5g/l) クロム酸(CrO3) 2.9g/l(Cr6+1.5g/l) 20%フッ化水素酸(HF) 3.0g/l(F-0.6g/l) pH1.5(塩酸で調整) 実施例4 実施例1と同一条件でアルミニウム合金を清浄後、化成
処理液4を50℃に加温して5秒間スプレー処理した。処
理後、実施例1と同一条件で水洗、乾燥、塗装し、性能
を評価した。
Chemical conversion treatment solution 3 40% fluorosilicic acid (H 2 SiF 6) 18.8g / l (SiF 6 2- 7.4g / l) 75% phosphoric acid (H 3 PO 4) 21.3g / l (PO 4 3- 15.5g / l) Chromic acid (CrO 3 ) 2.9g / l (Cr 6+ 1.5g / l) 20% Hydrofluoric acid (HF) 3.0g / l (F - 0.6g / l) pH1.5 (adjusted with hydrochloric acid Example 4 After cleaning the aluminum alloy under the same conditions as in Example 1, the chemical conversion treatment liquid 4 was heated to 50 ° C. and sprayed for 5 seconds. After the treatment, the performance was evaluated by washing with water, drying and coating under the same conditions as in Example 1.

化成処理液4 40%フルオロケイ酸(H4SiF6) 18.8g/l(SiF6 2-7.4g/l) 75%りん酸(H3PO4) 21.3g/l(PO4 3-15.5g/l) クロム酸(CrO3) 5.8g/l(Cr6+3.0g/l) 20%フッ化水素酸(HF) 5.0g/l(F-1.0g/l) pH2.0(水酸化ナトリウムで調整) 実施例5 実施例1と同一条件でアルミニウム合金を清浄後、化成
処理液5を50℃に加温して5秒間スプレー処理した。処
理後、実施例1と同一条件で水洗、乾燥、塗装し、性能
を評価した。
Chemical conversion treatment liquid 4 40% Fluorosilicic acid (H 4 SiF 6 ) 18.8g / l (SiF 6 2- 7.4g / l) 75% Phosphoric acid (H 3 PO 4 ) 21.3g / l (PO 4 3- 15.5g / l) Chromic acid (CrO 3 ) 5.8g / l (Cr 6+ 3.0g / l) 20% Hydrofluoric acid (HF) 5.0g / l (F - 1.0g / l) pH 2.0 (sodium hydroxide Example 5 After cleaning the aluminum alloy under the same conditions as in Example 1, the chemical conversion treatment liquid 5 was heated to 50 ° C. and sprayed for 5 seconds. After the treatment, the performance was evaluated by washing with water, drying and coating under the same conditions as in Example 1.

化成処理液5 フルオロホウ酸塩(NaBF4) 1.0g/l(BF4 -0.8g/l) 75%りん酸(H3PO4) 21.3g/l(PO4 3-15.5g/l) クロム酸(CrO3) 5.8g/l(Cr6+3.0g/l) 20%フッ化水素酸(HF) 3.0g/l(F-0.6g/l) pH2.0(水酸化アンモニウムで調整) 実施例6 実施例1と同一条件でアルミニウム合金を清浄後、化成
処理液6を50℃に加温して5秒間スプレー処理した。処
理後、実施例1と同一条件で水洗、乾燥、塗装し、性能
を評価した。
Chemical conversion solution 5 fluoroborate (NaBF 4) 1.0g / l ( BF 4 - 0.8g / l) 75% phosphoric acid (H 3 PO 4) 21.3g / l (PO 4 3- 15.5g / l) chromic acid (CrO 3 ) 5.8g / l (Cr 6+ 3.0g / l) 20% Hydrofluoric acid (HF) 3.0g / l (F - 0.6g / l) pH2.0 (adjusted with ammonium hydroxide) Example 6 After cleaning the aluminum alloy under the same conditions as in Example 1, the chemical conversion treatment liquid 6 was heated to 50 ° C. and spray-treated for 5 seconds. After the treatment, the performance was evaluated by washing with water, drying and coating under the same conditions as in Example 1.

化成処理液6 フルオロホウ酸塩(NaBF4) 2.0g/l(BF4 -1.6g/l) 75%りん酸(H3PO4) 21.3g/l(PO4 3-15.5g/l) クロム酸(CrO3) 5.8g/l(Cr6+3.0g/l) 20%フッ化水素酸(HF) 3.0g/l(F-0.6g/l) pH2.5(水酸化アンモニウムで調整) 実施例7 実施例1と同一条件でアルミニウム合金を清浄後、化成
処理液1を40℃に加温して10秒間スプレー処理した。処
理後、実施例1と同一条件で水洗、乾燥、塗装し、性能
を評価した。
Chemical conversion solution 6 fluoroborate (NaBF 4) 2.0g / l ( BF 4 - 1.6g / l) 75% phosphoric acid (H 3 PO 4) 21.3g / l (PO 4 3- 15.5g / l) chromic acid (CrO 3 ) 5.8g / l (Cr 6+ 3.0g / l) 20% Hydrofluoric acid (HF) 3.0g / l (F - 0.6g / l) pH2.5 (adjusted with ammonium hydroxide) Example 7. After cleaning the aluminum alloy under the same conditions as in Example 1, the chemical conversion treatment liquid 1 was heated to 40 ° C. and spray-treated for 10 seconds. After the treatment, the performance was evaluated by washing with water, drying and coating under the same conditions as in Example 1.

実施例8 実施例1と同一条件でアルミニウム合金を清浄後、化成
処理液1を50℃に加温して10秒間スプレー処理した。処
理後、実施例1と同一条件で水洗、乾燥、塗装し、性能
を評価した。
Example 8 After cleaning an aluminum alloy under the same conditions as in Example 1, the chemical conversion treatment liquid 1 was heated to 50 ° C. and spray-treated for 10 seconds. After the treatment, the performance was evaluated by washing with water, drying and coating under the same conditions as in Example 1.

比較例1 実施例1と同一条件でアルミニウム合金を清浄後、化成
処理液7を50℃に加温して5秒間スプレー処理した。処
理後、実施例1と同一条件で水洗、乾燥、塗装し、性能
を評価した。
Comparative Example 1 After cleaning an aluminum alloy under the same conditions as in Example 1, the chemical conversion treatment liquid 7 was heated to 50 ° C. and sprayed for 5 seconds. After the treatment, the performance was evaluated by washing with water, drying and coating under the same conditions as in Example 1.

化成処理液7 40%フルオロケイ酸(H2SiF6) 6.3g/l(SiF6 2-2.5g/l) 75%りん酸(H3PO4) 21.3g/l(PO4 3-15.5g/l) クロム酸(CrO3) 5.8g/l(Cr6+3.0g/l) 20%フッ化水素酸(HF) 3.0g/l(F-0.6g/l) pH2.0(水酸化アンモニウムで調整) 比較例2 実施例1と同一条件でアルミニウム合金を清浄後、化成
処理液8を50℃に加温して5秒間スプレー処理した。処
理後、実施例1と同一条件で水洗、乾燥、塗装し、性能
を評価した。
Chemical conversion treatment liquid 7 40% Fluorosilicic acid (H 2 SiF 6 ) 6.3g / l (SiF 6 2- 2.5g / l) 75% Phosphoric acid (H 3 PO 4 ) 21.3g / l (PO 4 3- 15.5g / l) Chromic acid (CrO 3 ) 5.8g / l (Cr 6+ 3.0g / l) 20% Hydrofluoric acid (HF) 3.0g / l (F - 0.6g / l) pH 2.0 (ammonium hydroxide Comparative Example 2 After cleaning the aluminum alloy under the same conditions as in Example 1, the chemical conversion treatment liquid 8 was heated to 50 ° C. and sprayed for 5 seconds. After the treatment, the performance was evaluated by washing with water, drying and coating under the same conditions as in Example 1.

化成処理液8 40%フルオロケイ酸(H2SiF6) 40.0g/l(SiF6 2-15.8g/l) 75%りん酸(H3PO4) 21.3g/l(PO4 3-15.5g/l) クロム酸(CrO3) 5.8g/l(Cr6+3.0g/l) 20%フッ化水素酸(HF) 3.0g/l(F-0.6g/l) pH2.0(水酸化アンモニウムで調整) 比較例3 実施例1と同一条件でアルミニウム合金を清浄後、市販
のりん酸のクロメート剤(登録商標アルクロム702、日
本パーカライジング株式会社製)の5%水溶液を50℃に
加温して5秒間スプレー処理した。処理後、実施例1と
同一条件で水洗、乾燥、塗装し、性能を評価した。
Chemical conversion solution 8 of 40% fluorosilicic acid (H 2 SiF 6) 40.0g / l (SiF 6 2- 15.8g / l) 75% phosphoric acid (H 3 PO 4) 21.3g / l (PO 4 3- 15.5g / l) Chromic acid (CrO 3 ) 5.8g / l (Cr 6+ 3.0g / l) 20% Hydrofluoric acid (HF) 3.0g / l (F - 0.6g / l) pH 2.0 (ammonium hydroxide Comparative Example 3 After cleaning an aluminum alloy under the same conditions as in Example 1, a commercially available 5% aqueous solution of a phosphoric acid chromate agent (registered trademark Alchrome 702, manufactured by Nihon Parkerizing Co., Ltd.) was heated to 50 ° C. Sprayed for 5 seconds. After the treatment, the performance was evaluated by washing with water, drying and coating under the same conditions as in Example 1.

比較例4 実施例1と同一条件でアルミニウム合金を清浄後、市販
のノンクロメート剤(登録商標パルコートK3761、日本
パーカライジング株式会社製)の2%水溶液を50℃に加
温して30秒間スプレー処理した。処理後、実施例1と同
一条件で水洗、乾燥、塗装し、性能を評価した。
Comparative Example 4 After cleaning an aluminum alloy under the same conditions as in Example 1, a 2% aqueous solution of a commercially available non-chromating agent (registered trademark Palcoat K3761, manufactured by Nihon Parkerizing Co., Ltd.) was heated to 50 ° C. and sprayed for 30 seconds. . After the treatment, the performance was evaluated by washing with water, drying and coating under the same conditions as in Example 1.

表1に示したように、本発明の化成処理液を用いること
により、優れた耐食性、塗料密着性が得られ、エナメル
フェザーにも優れることが理解できる。
As shown in Table 1, it can be understood that by using the chemical conversion treatment liquid of the present invention, excellent corrosion resistance and paint adhesion are obtained, and enamel feather is also excellent.

〔発明の効果〕〔The invention's effect〕

以上説明したように本発明に係るアルミニウムおよびア
ルミニウム合金用化成処理液は、りん酸イオン5.0〜40.
0g/l、6価クロムイオン1.0〜4.0g/lおよびフッ素イオ
ン0.1〜2.0g/l、フルオロケイ酸イオンを4.0〜15.0g/l
もしくはフルオロホウ酸イオンを0.5〜3.0g/lを含有
し、pHを1.0〜3.0にしたものであって、特にフルオロケ
イ酸もしくはフルオロホウ酸を配合させることにより、
塗装前のアルミニウムおよびアルミニウム合金の表面に
優れた耐食性と塗料密着性を有する化成皮膜が形成でき
るという優れた効果を奏する。
As described above, the chemical conversion treatment liquid for aluminum and aluminum alloys according to the present invention has a phosphate ion of 5.0 to 40.
0g / l, hexavalent chromium ion 1.0-4.0g / l and fluorine ion 0.1-2.0g / l, fluorosilicate ion 4.0-15.0g / l
Or, containing 0.5 to 3.0 g / l of fluoroborate ion and having a pH of 1.0 to 3.0, in particular, by incorporating fluorosilicic acid or fluoroboric acid,
It has an excellent effect that a chemical conversion film having excellent corrosion resistance and paint adhesion can be formed on the surface of aluminum and aluminum alloy before coating.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】りん酸イオン5.0〜40.0g/l、6価クロムイ
オン1.0〜4.0g/lおよびフッ素イオン0.1〜2.0g/l、フル
オロケイ酸イオンを4.0〜15.0g/lもしくはフルオロホウ
酸イオンを0.5〜3.0g/lを含有し、pHを1.0〜3.0にした
ことを特徴とするアルミニウムおよびアルミニウム合金
用化成処理液。
1. Phosphate ion 5.0 to 40.0 g / l, hexavalent chromium ion 1.0 to 4.0 g / l, fluorine ion 0.1 to 2.0 g / l, fluorosilicate ion 4.0 to 15.0 g / l or fluoroborate ion. Of 0.5 to 3.0 g / l and having a pH of 1.0 to 3.0. A chemical conversion treatment solution for aluminum and aluminum alloys.
JP2040168A 1990-02-21 1990-02-21 Chemical conversion treatment liquid for aluminum and aluminum alloys Expired - Lifetime JPH07100872B2 (en)

Priority Applications (8)

Application Number Priority Date Filing Date Title
JP2040168A JPH07100872B2 (en) 1990-02-21 1990-02-21 Chemical conversion treatment liquid for aluminum and aluminum alloys
DE69103139T DE69103139T2 (en) 1990-02-21 1991-02-13 METHOD AND COMPOSITIONS FOR THE CONVERSION TREATMENT OF ALUMINUM AND ALUMINUM ALLOYS.
AU73370/91A AU642478B2 (en) 1990-02-21 1991-02-13 Conversion treatment method and composition for aluminum and aluminum alloys
PCT/US1991/000965 WO1991013186A1 (en) 1990-02-21 1991-02-13 Conversion treatment method and composition for aluminum and aluminum alloys
BR919106049A BR9106049A (en) 1990-02-21 1991-02-13 WATER CONVERSION COATING SOLUTION, AND, PROCESS TO TREAT AN ALUMINUM SURFACE OR AN ALUMINUM ALLOY
US07/923,889 US5451271A (en) 1990-02-21 1991-02-13 Conversion treatment method and composition for aluminum and aluminum alloys
CA 2072592 CA2072592A1 (en) 1990-02-21 1991-02-13 Conversion treatment method and composition for aluminum and aluminum alloys
EP91904950A EP0516700B1 (en) 1990-02-21 1991-02-13 Conversion treatment method and composition for aluminum and aluminum alloys

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2040168A JPH07100872B2 (en) 1990-02-21 1990-02-21 Chemical conversion treatment liquid for aluminum and aluminum alloys

Publications (2)

Publication Number Publication Date
JPH03243781A JPH03243781A (en) 1991-10-30
JPH07100872B2 true JPH07100872B2 (en) 1995-11-01

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Country Link
JP (1) JPH07100872B2 (en)

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RU2495967C1 (en) * 2012-07-03 2013-10-20 Общество с ограниченной ответственностью "Научно-производственное предприятие "Уралавиаспецтехнология" Method of electrolyte-plasma grinding parts made from titanium alloys

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