JPH11151777A - Steel panel for highly corrosion resistant fuel tank - Google Patents

Steel panel for highly corrosion resistant fuel tank

Info

Publication number
JPH11151777A
JPH11151777A JP32142397A JP32142397A JPH11151777A JP H11151777 A JPH11151777 A JP H11151777A JP 32142397 A JP32142397 A JP 32142397A JP 32142397 A JP32142397 A JP 32142397A JP H11151777 A JPH11151777 A JP H11151777A
Authority
JP
Japan
Prior art keywords
lubricant
weight
resin
silica
corrosion resistance
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.)
Granted
Application number
JP32142397A
Other languages
Japanese (ja)
Other versions
JP3934763B2 (en
Inventor
Sachiko Suzuki
幸子 鈴木
Hiroyuki Ogata
浩行 尾形
Kazuo Mochizuki
一雄 望月
Hironari Tanabe
弘往 田辺
Osamu Ogawa
修 小川
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.)
JFE Steel Corp
Dai Nippon Toryo KK
Original Assignee
Dai Nippon Toryo KK
Kawasaki Steel 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 Dai Nippon Toryo KK, Kawasaki Steel Corp filed Critical Dai Nippon Toryo KK
Priority to JP32142397A priority Critical patent/JP3934763B2/en
Publication of JPH11151777A publication Critical patent/JPH11151777A/en
Application granted granted Critical
Publication of JP3934763B2 publication Critical patent/JP3934763B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/30Coatings combining at least one metallic layer and at least one inorganic non-metallic layer
    • C23C28/32Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one pure metallic layer
    • C23C28/322Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one pure metallic layer only coatings of metal elements only
    • C23C28/3225Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one pure metallic layer only coatings of metal elements only with at least one zinc-based layer
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C28/00Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of groups C23C2/00 - C23C26/00 or by combinations of methods provided for in subclasses C23C and C25C or C25D
    • C23C28/30Coatings combining at least one metallic layer and at least one inorganic non-metallic layer
    • C23C28/34Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one inorganic non-metallic material layer, e.g. metal carbide, nitride, boride, silicide layer and their mixtures, enamels, phosphates and sulphates
    • C23C28/345Coatings combining at least one metallic layer and at least one inorganic non-metallic layer including at least one inorganic non-metallic material layer, e.g. metal carbide, nitride, boride, silicide layer and their mixtures, enamels, phosphates and sulphates with at least one oxide layer

Landscapes

  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)
  • Laminated Bodies (AREA)
  • Other Surface Treatments For Metallic Materials (AREA)

Abstract

PROBLEM TO BE SOLVED: To provide the steel panel excellent not only in corrosion resistance (inner surface corrosion resistance) against alcohol itself or gasoline mixed with alcohol and formic acid but also in corrosion resistance (outer surface corrosion resistance) against atmospheric environment wherein thaw salt or sea salt particles come flying and having excellent press processability and resistance weldability. SOLUTION: Zn plating layers or metal plating layers 2 based on Zn are provided on both surfaces of a steel panel 1 as undermost layers and chromate layers 3 are provided on the upper surfaces of both layers 2. Further, a metal powder-containing lubricating org. resin layer 4 based on an amine modified epoxy resin, a particlate Ni powder, a lubricant and silica is provided on the upper surface of one of both layers 3 and a lubricating org. resin layer 5 on at least one resin having at least one functional group selected from a hydroxyl group, an isocyanate group, a carboxyl group, a glycidyl group and an amino group, a lubricant and silica is provided on the upper surface of the other one of the layers 3.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は燃料タンク用鋼板に
係り、特にアルコールそのものあるいはアルコールと蟻
酸の混合されたガソリンなどに対する耐食性(以下「内
面耐食性」と称す。)に優れるとともに、融雪塩あるい
は海塩粒子の飛来する大気環境に対する耐食性(以下
「外面耐食性」と称す。)に優れ、かつ、優れたプレス
加工性、抵抗溶接性を有する燃料タンク用鋼板に関す
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a steel plate for a fuel tank, and more particularly to a steel plate having excellent corrosion resistance to alcohol itself or gasoline mixed with alcohol and formic acid (hereinafter referred to as "inner surface corrosion resistance"), as well as snow melting salt or seawater. The present invention relates to a steel plate for a fuel tank that has excellent corrosion resistance to the air environment in which salt particles fly (hereinafter referred to as “outside corrosion resistance”) and has excellent press workability and resistance weldability.

【0002】[0002]

【従来の技術】従来、自動車用燃料としては、主にガソ
リンが用いられてきたが、近年、大気環境保全や価格な
どの観点から、アルコールあるいはアルコールとガソリ
ンを混合した燃料の検討も進められている。
2. Description of the Related Art Conventionally, gasoline has been mainly used as a fuel for automobiles. However, in recent years, studies have been made on alcohol or a mixture of alcohol and gasoline from the viewpoints of air environment protection and price. I have.

【0003】そこで、アルコール単独あるいはアルコー
ル混合ガソリン、とりわけ腐食性の強いアルコールと蟻
酸の混合されたガソリンに対する耐食性(内面耐食性)
と外の環境に対する耐食性(外面耐食性)を両立させる
ための提案が、特公平2−18981号、特公平2−1
8982号、特公平3−25349号などに開示されて
いる。
Therefore, the corrosion resistance (internal corrosion resistance) to alcohol alone or to gasoline mixed with alcohol, particularly gasoline mixed with highly corrosive alcohol and formic acid.
Proposals to achieve both corrosion resistance to the outside environment (external corrosion resistance) are disclosed in Japanese Patent Publication No. 2-19881 and Japanese Patent Publication No. 2-1.
No. 8982 and Japanese Patent Publication No. 3-25349.

【0004】すなわち、特公平2−18981号には、
Pb/Sn合金またはSnを主成分とする金属めっき
層、上層として金属粉末を含む有機樹脂皮膜を有する鋼
板が、特公平2−18982号、特公平3−25349
号には、ZnまたはZnを主成分とする金属めっき層、
上層として金属粉末を含む有機樹脂皮膜を有する鋼板が
記載されている。
That is, Japanese Patent Publication No. Hei 2-18981 discloses that
A steel plate having a metal plating layer containing a Pb / Sn alloy or Sn as a main component and an organic resin film containing a metal powder as an upper layer is disclosed in JP-B-2-18982 and JP-B-3-25349.
No., Zn or a metal plating layer containing Zn as a main component,
A steel sheet having an organic resin film containing a metal powder as an upper layer is described.

【0005】[0005]

【発明が解決しようとする課題】上記3つの公報に記載
されている金属粉末含有有機樹脂皮膜は、その有機樹脂
中の40〜90%がフェノキシ樹脂で占められている。
このフェノキシ樹脂自体は耐酸性、耐溶剤性に優れてい
るが、金属粉末との親和性が低いため、プレス加工時に
金属粉末の剥離が生じ、ダメージを受けた部分の内面耐
食性が悪くなる。またダメージを受けていない部分も、
樹脂/金属粉末間に燃料が滞留しやすくなり、内面耐食
性が悪くなる。また燃料タンクの外面側も、フェノキシ
樹脂と金属粉末との親和性不足に起因する耐食性劣化が
生じる。
The metal powder-containing organic resin films described in the above three publications have a phenoxy resin that accounts for 40 to 90% of the organic resin.
Although the phenoxy resin itself is excellent in acid resistance and solvent resistance, it has a low affinity for metal powder, so that the metal powder is peeled off during press working, and the inner surface corrosion resistance of the damaged portion deteriorates. Also, the parts that are not damaged,
The fuel easily stays between the resin and the metal powder, and the inner surface corrosion resistance deteriorates. Corrosion resistance is also deteriorated on the outer surface side of the fuel tank due to insufficient affinity between the phenoxy resin and the metal powder.

【0006】さらにいずれの鋼板も、樹脂皮膜が必須成
分として硬化剤を含むため、硬化度が高い場合には、熱
分解しづらく、ナゲット生成過程における被膜排除が困
難になり、抵抗溶接性が低下する。つまり、金属粉末に
より通電点を確保しても、残存する皮膜周辺の母材が溶
接不良を起こすため、充分なナゲット間のラップが得ら
れず燃料もれが生じる。場合により、充分な溶接強度が
得られず剥離が生じる。また、硬化度が低く未反応硬化
剤を含む場合には、その部分の凝集力の低さ、親水性な
どの理由で腐食因子(酸、塩素イオンなど)が侵入し易
く、耐食性が低下する。
Further, in any of the steel sheets, since the resin film contains a hardening agent as an essential component, when the degree of hardening is high, it is difficult to thermally decompose, it is difficult to remove the film during the nugget formation process, and the resistance weldability is reduced. I do. In other words, even if the energization point is secured by the metal powder, the base material around the remaining film causes poor welding, so that sufficient wrap between nuggets cannot be obtained and fuel leakage occurs. In some cases, sufficient welding strength cannot be obtained and peeling occurs. In addition, when the curing degree is low and an unreacted curing agent is contained, corrosion factors (acids, chloride ions, etc.) are likely to enter due to the low cohesive strength and hydrophilicity of the portion, and the corrosion resistance is reduced.

【0007】以上のように種々の性能不良を残しており
未だ実用化に至らない。したがって、本発明は、このよ
うな現行燃料タンク材料の欠点を解消し、アルコール、
特にメタノールそのものあるいはメタノールが酸化して
生成した蟻酸の混合されたガソリンに対する内面耐食性
と、融雪塩あるいは海塩粒子の飛来する大気環境に対す
る外面耐食性に優れ、かつ、燃料タンク製造過程におい
て優れたプレス加工性、抵抗溶接性を発揮する燃料タン
ク用鋼板を提供することを目的とする。
[0007] As described above, various performance defects remain, and they have not yet been put to practical use. Thus, the present invention overcomes these shortcomings of current fuel tank materials,
In particular, it has excellent internal corrosion resistance against gasoline mixed with methanol itself or formic acid generated by the oxidation of methanol, and has excellent external corrosion resistance against the atmospheric environment in which snow-melting salt or sea salt particles fly, and excellent press working in the fuel tank manufacturing process. An object of the present invention is to provide a steel plate for a fuel tank exhibiting resistance and resistance weldability.

【0008】[0008]

【課題を解決するための手段】発明者らは、主として有
機樹脂と金属粉末との親和性、有機樹脂自体の耐酸性、
および抵抗溶接性、潤滑性について鋭意検討した結果、
一方の面には、粒状Ni粉末とアミン変性エポキシ樹脂
と潤滑剤とシリカを主成分とする樹脂層、他方の面に
は、水酸基、イソシアネート基、カルボキシル基、グリ
シジル基およびアミノ基から選ばれた少なくとも1種の
官能基を有する少なくとも1種の樹脂とシリカと潤滑剤
を主成分とする樹脂層を用いることにより、上記の問題
を一挙に解決しうるという全く新たな知見を得て本発明
を完成したものである。
Means for Solving the Problems The present inventors mainly have an affinity between an organic resin and a metal powder, an acid resistance of the organic resin itself,
As a result of intensive studies on resistance weldability and lubricity,
On one surface, a resin layer mainly composed of granular Ni powder, an amine-modified epoxy resin, a lubricant and silica, and on the other surface, selected from a hydroxyl group, an isocyanate group, a carboxyl group, a glycidyl group and an amino group. By using a resin layer containing at least one kind of resin having at least one kind of functional group, silica and a lubricant as a main component, the present inventors have obtained a completely new finding that the above-mentioned problems can be solved at once and obtained the present invention. It is completed.

【0009】すなわち、本発明は、鋼板の両表面に最下
層としてZnまたはZnを主成分とする金属めっき層を
有し、その両方の上層にクロメート層を有し、さらにそ
の一方の面の上層にアミン変性エポキシ樹脂と、粒状N
i粉末と潤滑剤とシリカとを主成分とする金属粉末含有
潤滑性有機樹脂層を有し、かつ他方の面の上層に水酸
基、イソシアネート基、カルボキシル基、グリシジル基
およびアミノ基から選ばれた少なくとも1種の官能基を
有する少なくとも1種の樹脂と、潤滑剤と、シリカとを
主成分とする潤滑性有機樹脂層を有することを特徴とす
る高耐食性燃料タンク用鋼板を提供するものである。
That is, the present invention provides a steel plate having Zn or a metal plating layer containing Zn as a main component as a lowermost layer on both surfaces of the steel sheet, a chromate layer on both upper layers, and an upper layer on one of the surfaces. Amine-modified epoxy resin and granular N
i has a metal powder-containing lubricating organic resin layer containing a powder, a lubricant and silica as main components, and at least one selected from a hydroxyl group, an isocyanate group, a carboxyl group, a glycidyl group and an amino group on the other surface. An object of the present invention is to provide a steel plate for a highly corrosion-resistant fuel tank, comprising a lubricating organic resin layer containing at least one kind of resin having one kind of functional group, a lubricant and silica as main components.

【0010】また、前記金属粉末含有潤滑性有機樹脂層
が、アミン変性エポキシ樹脂100重量部に対して、粒
状Ni粉末が20〜400重量部、潤滑剤が0.1〜5
重量部、シリカが40重量部以下であるのが好ましい。
また、前記アミン変性エポキシ樹脂が、エポキシ基1当
量に対し、0.3〜1.0モルのアミン化合物を付加し
てなる複合体樹脂であり、かつ重量平均分子量が500
0〜50000の範囲であり、前記粒状Ni粉末が平均
粒径1〜9μmであり、前記潤滑剤が、ポリオレフィン
ワックスおよび/またはポリテトラフルオロエチレンで
あり、平均粒径1〜10μmであり、軟化点が70〜1
50℃であるのが好ましい。また、前記潤滑性有機樹脂
層が、前記樹脂100重量部に対して、潤滑剤が1〜4
0重量部と、シリカが5〜80重量部であるのが好まし
い。また、前記潤滑性有機樹脂層中の潤滑剤がポリオレ
フィンワックスおよび/またはポリテトラフルオロエチ
レンであり、該潤滑剤の軟化点が70〜150℃、かつ
平均粒径が1〜7μmであり、該潤滑性有機樹脂のガラ
ス転移温度(Tg)が0〜90℃であるのが好ましい。
[0010] The metal powder-containing lubricating organic resin layer is composed of 20 to 400 parts by weight of particulate Ni powder and 0.1 to 5 parts by weight of lubricant based on 100 parts by weight of the amine-modified epoxy resin.
It is preferred that the amount by weight of silica is 40 parts by weight or less.
The amine-modified epoxy resin is a composite resin obtained by adding 0.3 to 1.0 mol of an amine compound to 1 equivalent of an epoxy group, and has a weight average molecular weight of 500.
0 to 50,000, the granular Ni powder has an average particle size of 1 to 9 μm, the lubricant is a polyolefin wax and / or polytetrafluoroethylene, the average particle size is 1 to 10 μm, and the softening point is Is 70-1
Preferably it is 50 ° C. In addition, the lubricating organic resin layer contains a lubricant in an amount of 1-4 based on 100 parts by weight of the resin.
0 parts by weight and 5 to 80 parts by weight of silica are preferred. Further, the lubricant in the lubricating organic resin layer is polyolefin wax and / or polytetrafluoroethylene, the lubricant has a softening point of 70 to 150 ° C. and an average particle size of 1 to 7 μm. The glass transition temperature (Tg) of the conductive organic resin is preferably from 0 to 90 ° C.

【0011】[0011]

【発明の実施の形態】以下、本発明について説明する。
本発明の鋼板は、両面ともに3層からなる被覆層で形成
される。鋼板の最下層(第1層)とその上層(第2層)
の被覆構成は表裏とも同じとし、鋼板表面の第3層の被
覆層は燃料タンクの内面側に用いる一方の面と、外面側
に用いるもう一方の面とで異なるものとする。
DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention will be described below.
The steel sheet of the present invention is formed of a coating layer composed of three layers on both sides. Lowermost layer (first layer) and upper layer (second layer) of steel sheet
Is the same on both sides, and the third coating layer on the surface of the steel plate is different between one surface used on the inner surface side of the fuel tank and the other surface used on the outer surface side.

【0012】(金属めっき層)本発明の高耐食性燃料タ
ンク用鋼板は鋼板表面の最下層(第1層)としてZnま
たはZnを主成分とする金属めっき層を有する。該金属
めっき層は、アルコールおよびアルコール混合燃料中に
おいて鉄素地より卑な電位を示す金属層であるから、め
っき層が損傷したプレス加工部においてもZnの犠牲防
食作用により赤錆、穴あきの発生を抑制し、耐食性を向
上させる効果がある。
(Metal Plating Layer) The steel sheet for a highly corrosion resistant fuel tank of the present invention has a metal plating layer containing Zn or Zn as a main component as the lowermost layer (first layer) on the surface of the steel sheet. Since the metal plating layer is a metal layer showing a lower potential than the iron base material in alcohol and alcohol mixed fuel, red rust and perforation are suppressed by the sacrificial corrosion prevention effect of Zn even in the pressed part where the plating layer is damaged. And has the effect of improving corrosion resistance.

【0013】特に、Zn−Ni合金めっき、Zn−Co
合金めっき、Zn−Fe合金めっき、Zn−Al合金め
っき、Zn−Ni−Cr合金めっき、Zn−Ni−Co
合金めっきなどのZnを主成分とする金属めっき層は、
犠牲防食的な性能を維持しつつ、めっき層自体の耐食性
が高いため、さらに一層の耐穴あき性の向上が可能であ
る。これらのめっき層は、公知の電気めっき法や溶融め
っき法で形成される。
In particular, Zn-Ni alloy plating, Zn-Co
Alloy plating, Zn-Fe alloy plating, Zn-Al alloy plating, Zn-Ni-Cr alloy plating, Zn-Ni-Co
The metal plating layer mainly composed of Zn, such as alloy plating,
Since the corrosion resistance of the plating layer itself is high while maintaining the sacrificial anticorrosion performance, it is possible to further improve the perforation resistance. These plating layers are formed by a known electroplating method or hot-dip plating method.

【0014】このようなZnまたはZnを主成分とする
金属めっき層の目付量は10〜200g/m2 が好まし
い。より好ましくは20〜100g/m2 である。めっ
き目付量が10g/m2 未満では鋼板表面の隠蔽効果が
不充分となり、下層に必要とされる耐食性が不足する。
また200g/m2 を超えると下層に必要とされる耐食
性が飽和する。めっき層の目付量は、燃料タンクの内面
に用いる側と外面に用いる側で同一でもよいが、外面耐
食性向上の理由から外面側のめっき厚みを内面側よりも
厚くしてもよい。
The basis weight of Zn or a metal plating layer containing Zn as a main component is preferably from 10 to 200 g / m 2 . More preferably, it is 20 to 100 g / m 2 . When the basis weight of plating is less than 10 g / m 2 , the effect of hiding the steel sheet surface becomes insufficient, and the corrosion resistance required for the lower layer becomes insufficient.
If it exceeds 200 g / m 2 , the corrosion resistance required for the lower layer is saturated. The basis weight of the plating layer may be the same on the side used for the inner surface and the side used for the outer surface of the fuel tank, but the plating thickness on the outer surface may be larger than that on the inner surface for the purpose of improving the outer corrosion resistance.

【0015】(クロメート層)次に第2層(金属めっき
の上層)として、表裏の両面ともクロメート層を形成さ
せる。クロメート層は、ZnあるいはZnを主成分とす
る金属めっき層と最上層の樹脂層の接着性を向上させる
ために形成させる。クロメート層はクロム水和酸化物を
主要構成成分とした、3価クロムと6価クロムからなる
被膜である。
(Chromate layer) Next, a chromate layer is formed on both front and back surfaces as a second layer (upper layer of metal plating). The chromate layer is formed to improve the adhesion between Zn or a metal plating layer containing Zn as a main component and the uppermost resin layer. The chromate layer is a coating composed of trivalent chromium and hexavalent chromium containing chromium hydrated oxide as a main component.

【0016】クロメート層の付着量は、金属クロム換算
で片面あたり5〜200mg/m2が好ましい。より好
ましくは10〜100mg/m2 である。5mg/m2
未満の場合、その上層の有機皮膜との密着性が不足する
ため、プレス加工時、摺動部の皮膜が剥離し、場合によ
ってはめっき層の剥離まで発生する。また付着量が少な
いために自己修復に用いられるべき6価クロム成分が不
足し、かつ前記めっき層の剥離と相まって内外面の加工
部の耐食性が不足する。200mg/m2 超える場合、
クロメート層自体が非常に脆くなり、加工部でクロメー
ト層の剥離が発生し、これに伴うその上層の有機皮膜の
剥離も生じる。このため、内外面の加工部の耐食性が不
足する。クロメート層の付着量は、燃料タンクの内面に
用いる側と外面に用いる側で同一でも異なっていてもよ
い。
The amount of the chromate layer deposited is preferably 5 to 200 mg / m 2 per one surface in terms of chromium metal. More preferably, it is 10 to 100 mg / m 2 . 5 mg / m 2
If it is less than 30, the adhesion to the upper organic film is insufficient, so that the film on the sliding portion is peeled off during press working, and in some cases, the plating layer is peeled off. Further, since the amount of adhesion is small, the hexavalent chromium component to be used for self-healing is insufficient, and the corrosion resistance of the processed portion on the inner and outer surfaces is insufficient due to the peeling of the plating layer. If it exceeds 200 mg / m 2 ,
The chromate layer itself becomes very brittle, the chromate layer peels off at the processed part, and the accompanying organic film peels off. For this reason, the corrosion resistance of the processed portions on the inner and outer surfaces is insufficient. The attachment amount of the chromate layer may be the same or different between the side used for the inner surface and the side used for the outer surface of the fuel tank.

【0017】そして最上層(第3層)として、一方の面
は粒状Ni粉末、アミン変性エポキシ、潤滑剤、シリカ
を主成分とする金属粉末含有潤滑性有機樹脂で被覆し、
他方の面は樹脂、シリカ、潤滑剤からなる潤滑性有機樹
脂で被覆する。金属粉末含有潤滑性有機樹脂は耐食性、
溶接性、潤滑性等に優れ、燃料タンクの内面側(すなわ
ちガソリンと接する側)として用いるのが好ましく、潤
滑性有機樹脂は耐食性、潤滑性に優れるので、燃料タン
クの外面側として用いるのが好ましい。
As the uppermost layer (third layer), one surface is coated with a granular Ni powder, an amine-modified epoxy, a lubricant, a lubricating organic resin containing a metal powder containing silica as a main component,
The other surface is covered with a lubricating organic resin composed of a resin, silica and a lubricant. Lubricant organic resin containing metal powder is corrosion resistant,
It is excellent in weldability, lubricity, etc., and is preferably used as the inner side of the fuel tank (that is, the side in contact with gasoline). Lubricating organic resin is preferably used as the outer side of the fuel tank because it has excellent corrosion resistance and lubricity. .

【0018】(金属粉末含有潤滑性有機樹脂層)金属粉
末含有潤滑性有機樹脂層は、アルコール特にメタノール
そのものあるいはメタノールが酸化して生成した蟻酸の
混合されたガソリンに対してすぐれた耐食性を有する金
属粉末と樹脂成分からなり、金属めっき層およびクロメ
ート層とアルコール系燃料との直接接触を阻止するため
の防食層の役目をはたす。
(Metal Powder-Containing Lubricating Organic Resin Layer) The metal powder-containing lubricating organic resin layer is a metal having excellent corrosion resistance to alcohol, particularly methanol itself, or gasoline mixed with formic acid formed by oxidizing methanol. It is composed of a powder and a resin component, and serves as an anticorrosion layer for preventing direct contact between the metal plating layer and the chromate layer and the alcohol fuel.

【0019】(アミン変性エポキシ樹脂)本発明で用い
られる樹脂成分は、いうまでもなくガソリンやアルコー
ル系燃料に対してすぐれた耐食性を有し、かつクロメー
ト層に対する塗膜密着性、プレス加工性においてすぐれ
た特性を発揮するものである。すなわち、アミン変性エ
ポキシ樹脂を用いることにより、すぐれたプレス加工性
とアルコール系燃料に対する耐食性およびクロメート層
に対する塗膜密着性が確保される。
(Amine-Modified Epoxy Resin) Needless to say, the resin component used in the present invention has excellent corrosion resistance to gasoline and alcohol-based fuels, and has excellent coating film adhesion to a chromate layer and press workability. It exhibits excellent characteristics. That is, by using the amine-modified epoxy resin, excellent press workability, corrosion resistance to alcohol-based fuel, and coating film adhesion to the chromate layer are ensured.

【0020】アミン変性エポキシ樹脂は、エポキシ樹脂
をアミン化合物で変性したものであり好ましくはエポキ
シ樹脂の末端をアミン化合物で変性したものであり、さ
らに好ましくは両末端をアミン化合物で変性したもので
ある。ここで、エポキシ樹脂は、ビスフェノールA型エ
ポキシ樹脂、ビスフェノールF型エポキシ樹脂、環状脂
肪族エポキシ樹脂、ヒダントイン型エポキシ樹脂、ノボ
ラック型エポキシ樹脂、グリシジルエステル型エポキシ
樹脂等を挙げることができる。これらのエポキシ樹脂の
エポキシ当量は180〜5000が好ましい。具体例は
エピコート1010、1009、1007、1004、
1001(いずれも油化シェルエポキシ(株)製)など
を挙げることができる。これらは単独で用いてもよく、
2種以上を混合して用いてもよい。また、ビスフェノー
ルA型エポキシ樹脂、ビスフェノールF型エポキシ樹脂
などのビスフェノール型エポキシ樹脂と、ビスフェノー
ルAまたはビスフェノールFとを反応させた反応生成物
を用いても良い。これらのうち、塗料としての安定性や
プレス加工性、内面耐食性を安定して得るための製造条
件範囲の広さからビスフェノールA型エポキシ樹脂、ビ
スフェノールF型エポキシ樹脂やビスフェノール型エポ
キシ樹脂とビスフェノールAまたはビスフェノールFと
を反応させたものが好ましい。
The amine-modified epoxy resin is a resin obtained by modifying an epoxy resin with an amine compound, preferably a resin obtained by modifying the terminal of an epoxy resin with an amine compound, and more preferably a compound obtained by modifying both terminals with an amine compound. . Here, examples of the epoxy resin include a bisphenol A epoxy resin, a bisphenol F epoxy resin, a cycloaliphatic epoxy resin, a hydantoin epoxy resin, a novolak epoxy resin, and a glycidyl ester epoxy resin. The epoxy equivalent of these epoxy resins is preferably from 180 to 5,000. Specific examples are Epicoat 1010, 1009, 1007, 1004,
1001 (all manufactured by Yuka Shell Epoxy Co., Ltd.) and the like. These may be used alone,
Two or more kinds may be used as a mixture. Further, a reaction product obtained by reacting a bisphenol type epoxy resin such as a bisphenol A type epoxy resin or a bisphenol F type epoxy resin with bisphenol A or bisphenol F may be used. Among these, bisphenol A type epoxy resin, bisphenol F type epoxy resin and bisphenol type epoxy resin and bisphenol A or bisphenol A from the wide range of manufacturing conditions for stably obtaining paint stability, press workability, and inner surface corrosion resistance What reacted with bisphenol F is preferable.

【0021】アミン化合物は、n−プロピルアミン、i
so−プロピルアミン、n−ブチルアミン、sec−ブ
チルアミン、tert−ブチルアミン、ジエチルアミ
ン、エチレンジアミン、ジエチレントリアミン、トリエ
チレンジアミン、テトラエチレンジアミン、プロピレン
ジアミン、N−メチルピペラジン、エタノールアミン、
ジエタノールアミン、N−メチルエタノールアミン、i
so−プロパノールアミン、ジイソプロパノールアミ
ン、n−プロパノールアミン、エチルエタノールアミ
ン、3−メタノールピペリジンなどを挙げることができ
る。このうち特に好ましくは、アルカノールアミンやジ
アルカノールアミンである。
The amine compound is n-propylamine, i
so-propylamine, n-butylamine, sec-butylamine, tert-butylamine, diethylamine, ethylenediamine, diethylenetriamine, triethylenediamine, tetraethylenediamine, propylenediamine, N-methylpiperazine, ethanolamine,
Diethanolamine, N-methylethanolamine, i
Examples thereof include so-propanolamine, diisopropanolamine, n-propanolamine, ethylethanolamine, and 3-methanolpiperidine. Of these, alkanolamine and dialkanolamine are particularly preferred.

【0022】エポキシ樹脂のエポキシ基1当量に付加す
るアミン化合物のモル数は0.3〜1.0モル、さらに
は0.5〜0.8モルが好ましい。アミン化合物のモル
数が0.3未満の場合、アミン変性度が不足するため、
金属粉末とエポキシ樹脂の親和性が低下し、プレス加工
時に金属粉末が皮膜から脱離する。その程度が激しい場
合には、めっき層の剥離が生じるため、プレス加工性が
劣る。また同様の理由から皮膜中の樹脂/金属粉末間に
腐食液が滞留しやすくなり、充分な疎水性が得られず蟻
酸水溶液を皮膜中に呼び込み易いことも要因となって、
腐食性の強いメタノール系燃料に対する内面耐食性が不
足する。アミン化合物のモル数が1.0モルを超えると
その超えた分はエポキシ基に付加せず経済的ではなく、
余剰アミンが吸水性を高め内面耐食性が低下する。
The number of moles of the amine compound added to one equivalent of the epoxy group of the epoxy resin is preferably 0.3 to 1.0 mole, more preferably 0.5 to 0.8 mole. If the number of moles of the amine compound is less than 0.3, the degree of amine modification is insufficient,
The affinity between the metal powder and the epoxy resin is reduced, and the metal powder is detached from the film during press working. If the degree is severe, peeling of the plating layer occurs, resulting in poor press workability. For the same reason, the corrosive liquid tends to stay between the resin and the metal powder in the film, and it is difficult to obtain sufficient hydrophobicity, so that formic acid aqueous solution is easily introduced into the film.
Insufficient internal corrosion resistance to highly corrosive methanol fuel. When the number of moles of the amine compound exceeds 1.0 mole, the excess is not economical without being added to the epoxy group,
Excess amine increases water absorption and lowers inner corrosion resistance.

【0023】アミン変性エポキシ樹脂の重量平均分子量
は5000〜50000が好ましく、さらに好ましくは
10000〜40000である。分子量が5000未満
の場合、樹脂の分子量が低すぎるため、分子間が不足
し、皮膜の強靱性が低下する。このため、プレス加工時
に皮膜が削られ、プレス加工性が低下する。分子量が5
0000超の場合、エポキシ基に付加されているアミン
の量が少なくなるため、樹脂と金属粉末との親和性が不
足し、プレス加工時に皮膜からの金属粉の脱離が発生し
たり、内面耐食性が不足する。
The weight average molecular weight of the amine-modified epoxy resin is preferably from 5,000 to 50,000, more preferably from 10,000 to 40,000. When the molecular weight is less than 5,000, the molecular weight of the resin is too low, so that the intermolecular distance is insufficient and the toughness of the film is reduced. For this reason, the film is shaved during the press working, and the press workability is reduced. Molecular weight 5
If it is more than 0000, the amount of amine added to the epoxy group is small, so that the affinity between the resin and the metal powder is insufficient, the metal powder is detached from the film at the time of press working, and the inner surface has corrosion resistance. Run out.

【0024】(粒状Ni粉末)粒状Ni粉末添加の目的
は、抵抗溶接性の向上である。すなわち有機樹脂皮膜は
一般に高い電気絶縁性を有し、しかも樹脂皮膜の膜厚は
約0.5〜9μm位であるため、鋼板の凸部の露出を全
く期待できず、抵抗溶接が困難である。そこで本発明は
ガソリンタンク内面側の有機樹脂皮膜中に、金属粉末を
必要量分散させ、皮膜の電導性を高めるのである。また
後述するシリカとの組合せにより、耐食性も向上する。
Niはメタノールに対して耐食性が優れかつ固有抵抗が
高いため最も有用である。特に粒状Ni粉末のみを添加
するのが好ましい。
(Granular Ni Powder) The purpose of adding granular Ni powder is to improve resistance weldability. That is, since the organic resin film generally has high electrical insulation and the thickness of the resin film is about 0.5 to 9 μm, exposure of the convex portion of the steel sheet cannot be expected at all, and resistance welding is difficult. . Therefore, in the present invention, a required amount of metal powder is dispersed in the organic resin film on the inner surface side of the gasoline tank to enhance the conductivity of the film. In addition, the combination with silica described below also improves corrosion resistance.
Ni is most useful because of its excellent corrosion resistance and high specific resistance to methanol. In particular, it is preferable to add only granular Ni powder.

【0025】粒状Ni粉末の寸法は平均粒径1〜9μm
の粒状のものが好ましい。より好ましくは2〜7μmで
ある。平均粒径が1μm未満の場合、通電点が不足す
る。平均粒径が9μm超えの場合、通電点は充分に有す
るため、少量の添加で抵抗溶接性が向上する。ところ
が、皮膜が多孔質になるため、内面耐食性が低下し、さ
らにはプレス加工時における皮膜のパウダリングも問題
になる。粒状Ni粉末の添加量は、アミン変性エポキシ
樹脂100重量部に対して20〜400重量部、好まし
くは30〜100重量部である。20重量部未満の場
合、通電点が不足し電導性に劣るため抵抗溶接性が低下
するからである。400重量部超えの場合、有機皮膜自
体が脆弱になりプレス時の耐パウダリング性が低下し内
面耐食性が低下する。
The size of the granular Ni powder is 1-9 μm in average particle size.
Are preferred. More preferably, it is 2 to 7 μm. If the average particle size is less than 1 μm, the number of current-carrying points is insufficient. When the average particle size is more than 9 μm, the current-carrying point is sufficient, so that the addition of a small amount improves the resistance weldability. However, since the film is porous, the corrosion resistance on the inner surface is reduced, and powdering of the film at the time of press working also poses a problem. The amount of the granular Ni powder to be added is 20 to 400 parts by weight, preferably 30 to 100 parts by weight, based on 100 parts by weight of the amine-modified epoxy resin. If the amount is less than 20 parts by weight, the current-carrying point is insufficient and the conductivity is poor, so that the resistance weldability is reduced. If the amount exceeds 400 parts by weight, the organic film itself becomes brittle, powdering resistance during pressing decreases, and inner surface corrosion resistance decreases.

【0026】本発明では、粒状Ni粉末を、シランカッ
プリング剤で表面処理することが好ましい。シランカッ
プリング剤で金属粉末を表面処理をすると、アミン変性
エポキシ樹脂との親和性、反応性が高まり、両者の結合
が強固となるため、アルコール、蟻酸などの侵入を防止
し、耐食性が向上する。さらに、プレス加工時のパウダ
リング性も向上する。シランカップリング剤としては、
エポキシシラン、ビニルシラン、メルカプトシラン、ア
ミノシランなどを例示することができる。この中でもア
ミノシラン、エポキシシランが好適である。アミノシラ
ンカップリング剤としては、N−β(アミノエチル)−
γ−アミノプロピルトリメトキシシラン、γ−アミノプ
ロピルトリエトキシシラン、N−フェニル−γ−アミノ
プロピルトリメトキシシランなどが好適である。エポキ
シシランカップリング剤としては、β−(3,4−エポ
キシシクロヘキシル)エチルトリメトキシシラン、γ−
グリシドキシプロピルトリメトキシシラン、γ−グリシ
ドキシプロピルメチルジエトキシシランなどが好適であ
る。シランカップリング剤の表面処理方法は公知の方法
で行なうことができる。
In the present invention, it is preferable to subject the granular Ni powder to a surface treatment with a silane coupling agent. When the metal powder is surface-treated with a silane coupling agent, the affinity and reactivity with the amine-modified epoxy resin are increased, and the bond between the two is strengthened, thereby preventing the intrusion of alcohol, formic acid, etc., and improving the corrosion resistance. . Further, the powdering property at the time of press working is also improved. As a silane coupling agent,
Epoxy silane, vinyl silane, mercapto silane, amino silane and the like can be exemplified. Among them, aminosilane and epoxysilane are preferred. As an aminosilane coupling agent, N-β (aminoethyl)-
γ-aminopropyltrimethoxysilane, γ-aminopropyltriethoxysilane, N-phenyl-γ-aminopropyltrimethoxysilane and the like are preferred. Examples of the epoxysilane coupling agent include β- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, γ-
Glycidoxypropyltrimethoxysilane, γ-glycidoxypropylmethyldiethoxysilane and the like are preferred. The surface treatment of the silane coupling agent can be performed by a known method.

【0027】(潤滑剤)内面の有機樹脂皮膜に自己潤滑
性を付与するため、潤滑剤が添加される。本発明では、
潤滑剤を有機皮膜表面に突出させることにより、プレス
加工時に鋼板と金型の摩擦を低減し、樹脂皮膜の損傷を
防止する。このような潤滑剤として、ポリエチレン系、
ポリプロピレン系、ポリブテン系などのポリオレフィン
ワックスやポリテトラフルオロエチレンなどが好まし
い。これらは単独で用いてもよく、2種以上を混合して
もよい。これらは潤滑性が優れると共に、ガソリン、ア
ルコール、蟻酸、潤滑油などの耐薬品性に優れるので好
ましい。
(Lubricant) A lubricant is added to impart self-lubricating property to the organic resin film on the inner surface. In the present invention,
By projecting the lubricant onto the surface of the organic film, friction between the steel plate and the mold during press working is reduced, and damage to the resin film is prevented. As such a lubricant, polyethylene-based,
Polyolefin waxes such as polypropylene and polybutene and polytetrafluoroethylene are preferred. These may be used alone or as a mixture of two or more. These are preferred because they have excellent lubricity and excellent chemical resistance to gasoline, alcohol, formic acid, lubricating oil and the like.

【0028】潤滑剤の平均粒径は1〜10μmが好まし
く、さらに好ましくは2〜8μmである。平均粒径が1
μm未満の場合、有機皮膜から突出する潤滑剤の量が少
なくプレス加工性が低下する。10μm超えの場合、プ
レス加工時に皮膜から脱離し易くなる。潤滑剤の軟化点
は、70〜150℃が好ましい。異なる軟化点のものを
混合しても良い。軟化点が70℃未満の場合、発熱を伴
う過酷なプレス条件下では、潤滑剤の弾性率が著しく低
下し、プレス加工性が劣る。軟化点が150℃超えの場
合、潤滑剤の軟化が不足し、プレス加工性が劣る。潤滑
剤の添加量はアミン変性エポキシ樹脂100重量部に対
して、0.1〜5重量部が好ましい。より好ましくは
0.1〜4重量部である。0.1重量部未満では、潤滑
性が不足し、プレス加工時に皮膜がダメージを受けるた
め、耐食性が低下する。5重量部を超えると、プレス加
工時に潤滑剤の脱離が生じやすくなり、耐食性が悪くな
る。
The average particle size of the lubricant is preferably 1 to 10 μm, more preferably 2 to 8 μm. Average particle size is 1
When it is less than μm, the amount of the lubricant projecting from the organic film is small and the press workability is reduced. If it exceeds 10 μm, it is easy to detach from the film during press working. The softening point of the lubricant is preferably from 70 to 150C. Those having different softening points may be mixed. When the softening point is less than 70 ° C., under severe pressing conditions involving heat generation, the elastic modulus of the lubricant is significantly reduced, and press workability is poor. When the softening point is higher than 150 ° C., the softening of the lubricant is insufficient, and the press workability is poor. The amount of the lubricant is preferably 0.1 to 5 parts by weight based on 100 parts by weight of the amine-modified epoxy resin. It is more preferably 0.1 to 4 parts by weight. If the amount is less than 0.1 part by weight, the lubricating property is insufficient, and the film is damaged during the press working, so that the corrosion resistance is reduced. If the amount exceeds 5 parts by weight, desorption of the lubricant is likely to occur during press working, and the corrosion resistance deteriorates.

【0029】(シリカ)シリカは必須である。シリカ表
面のシラノール基がクロメート層や有機皮膜中の他の成
分との反応などが生じ、皮膜の密着性が向上したり、耐
食性が良好になる。シリカは、コロイダルシリカ(例え
ば、日産化学(株)製スノーテックス−Oやスノーテッ
クス−N)、オルガノシリカゾル(例えば、日産化学
(株)製エチルセロソルブシリカゾル)、シリカ粉末
(例えば、アエロジル(株)製気相シリカ粉末)や自身
が縮合することによりシリカになる有機シリケート(例
えば、エチルシリケート等を酸触媒と併用して用いる)
等を用いることができる。シリカ粉末の粒径は、シリカ
を均一に分散させるために5〜70nmが好ましい。
(Silica) Silica is essential. The silanol group on the silica surface reacts with the chromate layer and other components in the organic film, and the like, thereby improving the adhesion of the film and improving the corrosion resistance. Silica is colloidal silica (for example, Snowtex-O or Snowtex-N manufactured by Nissan Chemical Co., Ltd.), organosilica sol (for example, ethyl cellosolve silica sol manufactured by Nissan Chemical Co., Ltd.), silica powder (for example, Aerosil Co., Ltd.) Organic silicate which becomes silica by condensing itself (for example, gas-phase silica powder) (for example, ethyl silicate is used in combination with an acid catalyst)
Etc. can be used. The particle size of the silica powder is preferably from 5 to 70 nm in order to uniformly disperse the silica.

【0030】シリカの添加量は、アミン変性エポキシ樹
脂100重量部に対して、40重量部以下、さらには5
〜20重量部が好ましい。40重量部超の場合、皮膜の
プレス加工性が低下し、皮膜にクラックが生じやすくな
り、その結果耐食性が悪くなる。シリカが添加されてい
ない場合、耐食性が低下する。またその他の添加剤とし
て、顔料、チクソトロピック剤、分散剤、揺変剤、沈殿
防止剤等の添加剤を皮膜中に添加することもできる。金
属粉末含有潤滑性樹脂の平均厚みは乾燥後0.5〜9μ
mが好ましい。0.5μm未満では外層として要求され
る内面耐食性が不充分である。9μmを超えると、耐食
性が飽和し、プレス加工性、シーム溶接性が低下する。
The amount of silica added is 40 parts by weight or less, and more preferably 5 parts by weight, based on 100 parts by weight of the amine-modified epoxy resin.
-20 parts by weight are preferred. If the amount exceeds 40 parts by weight, the press workability of the film is reduced, and the film is easily cracked, resulting in poor corrosion resistance. When silica is not added, the corrosion resistance decreases. Further, as other additives, additives such as a pigment, a thixotropic agent, a dispersant, a thixotropic agent, and a suspending agent can be added to the film. The average thickness of the metal powder-containing lubricating resin is 0.5 to 9μ after drying.
m is preferred. If it is less than 0.5 μm, the internal corrosion resistance required for the outer layer is insufficient. If it exceeds 9 μm, the corrosion resistance is saturated, and the press workability and the seam weldability deteriorate.

【0031】この皮膜の形成方法の一例を示す。アミン
変性エポキシ樹脂は、エポキシ樹脂を各種有機溶剤(炭
化水素系、エステル系、ケトン系、アルコール系、エー
テル系など)に溶解させた後、アミン化合物を添加し、
常温〜100℃で4〜5時間反応させることにより得ら
れる。次に得られたアミン変性エポキシ樹脂溶液に、金
属粉末、潤滑剤、シリカ、その他添加剤を添加し、サン
ドミル、アトライターなどでこれらを分散させ、金属粉
含有潤滑性有機樹脂塗料を作成する。塗料はロールコー
タ、バーコータなどの公知の方法で塗布し、150〜3
00℃で乾燥する。
An example of a method for forming this film will be described. The amine-modified epoxy resin is prepared by dissolving the epoxy resin in various organic solvents (such as hydrocarbons, esters, ketones, alcohols, and ethers), and then adding an amine compound.
It is obtained by reacting at room temperature to 100 ° C for 4 to 5 hours. Next, a metal powder, a lubricant, silica, and other additives are added to the obtained amine-modified epoxy resin solution, and these are dispersed with a sand mill, an attritor, or the like to prepare a metal powder-containing lubricating organic resin paint. The coating is applied by a known method such as a roll coater or a bar coater,
Dry at 00 ° C.

【0032】(潤滑性有機樹脂層)次に潤滑性有機樹脂
層について説明する。 (有機樹脂)潤滑性有機樹脂層はシリカが複合された潤
滑性樹脂層である。ここで使用する有機樹脂は、水酸
基、イソシアネート基、カルボキシル基、グリシジル基
およびアミノ基から選ばれた少なくとも1種の官能基を
有する少なくとも1種の樹脂であればよい。具体的に
は、エポキシ樹脂、アルキッド樹脂、アクリル樹脂、ウ
レタン樹脂、ポリビニルブチラール樹脂、フェノール樹
脂、メラミン樹脂等が挙げられる。これらのうち、耐食
性などの点からポリビニルブチラール樹脂が好ましい。
(Lubricating Organic Resin Layer) Next, the lubricating organic resin layer will be described. (Organic resin) The lubricating organic resin layer is a lubricating resin layer in which silica is composited. The organic resin used here may be at least one resin having at least one functional group selected from a hydroxyl group, an isocyanate group, a carboxyl group, a glycidyl group and an amino group. Specific examples include an epoxy resin, an alkyd resin, an acrylic resin, a urethane resin, a polyvinyl butyral resin, a phenol resin, and a melamine resin. Among them, polyvinyl butyral resin is preferable from the viewpoint of corrosion resistance and the like.

【0033】(潤滑剤)外面の有機樹脂皮膜に自己潤滑
性を付与するため、潤滑剤が添加される。本発明では、
潤滑剤を有機皮膜表面に突出させることにより、成形時
に鋼板と金型の摩擦を低減し、樹脂皮膜の損傷を防止す
る。潤滑剤としては金属粉末含有潤滑性有機樹脂層で前
述したものが使用可能であり、潤滑剤の融点の好適範囲
も前述の通りである。
(Lubricant) A lubricant is added for imparting self-lubricating property to the organic resin film on the outer surface. In the present invention,
By projecting the lubricant on the surface of the organic film, friction between the steel plate and the mold during molding is reduced, and damage to the resin film is prevented. As the lubricant, those described above for the metal powder-containing lubricating organic resin layer can be used, and the preferable range of the melting point of the lubricant is also as described above.

【0034】潤滑剤の平均粒径は1〜7μmが好まし
く、さらに好ましくは2〜6μmである。平均粒径が1
μm未満の場合、有機皮膜から突出する潤滑剤の量が少
なくプレス加工性が低下する。7μm超えの場合、プレ
ス加工時に皮膜から脱離し易くなる。外面に用いる潤滑
性有機樹脂層中の潤滑剤の粒径が、内面に使用する金属
粉末含有潤滑性有機樹脂層中の潤滑剤の粒径よりも小さ
いのは、内面皮膜に比べて外面皮膜が薄いためである。
潤滑剤の添加量は、水酸基、イソシアネート基、カルボ
キシル基、グリシジル基およびアミノ基から選ばれた少
なくとも1種の官能基を有する少なくとも1種の樹脂1
00重量部に対して、1〜40重量部、さらには5〜2
0重量部が好ましい。1重量部未満では、潤滑性が不足
し、プレス加工時に皮膜がダメージを受けるため、耐食
性が低下する。40重量部を超えると、プレス加工時に
潤滑剤の脱離が生じやすくなり、耐食性が悪くなる。外
面皮膜には金属粉末が添加されていないため、内面皮膜
よりも多量の潤滑剤の添加が可能である。また、プレス
加工時には外面側の方がダメージを受けやすいので、内
面側よりも多くの潤滑剤を添加する方が好ましい。
The average particle size of the lubricant is preferably from 1 to 7 μm, more preferably from 2 to 6 μm. Average particle size is 1
When it is less than μm, the amount of the lubricant projecting from the organic film is small and the press workability is reduced. When it exceeds 7 μm, it is easy to detach from the film during press working. The reason why the particle size of the lubricant in the lubricating organic resin layer used on the outer surface is smaller than the particle size of the lubricant in the lubricating organic resin layer containing the metal powder used on the inner surface is that the outer film has a smaller particle size than the inner film. Because it is thin.
The amount of the lubricant added is at least one resin having at least one functional group selected from a hydroxyl group, an isocyanate group, a carboxyl group, a glycidyl group and an amino group.
1 to 40 parts by weight, and more preferably 5-2 to 100 parts by weight
0 parts by weight is preferred. If the amount is less than 1 part by weight, the lubricity is insufficient, and the film is damaged at the time of press working, so that the corrosion resistance is reduced. If the amount exceeds 40 parts by weight, desorption of the lubricant is likely to occur during press working, and the corrosion resistance deteriorates. Since no metal powder is added to the outer coating, a larger amount of lubricant can be added than the inner coating. In addition, during press working, the outer surface side is more likely to be damaged, so it is preferable to add more lubricant than the inner surface side.

【0035】(シリカ)シリカの添加は、シリカ表面の
シラノール基と前述の樹脂やクロメート層と反応させ、
高耐食性を有する無機−有機複合皮膜を形成させ、タン
ク外面の有機樹脂皮膜の密着性を向上させ耐食性を向上
させるからである。シリカとしては、前述したものが使
用可能である。シリカの添加量は、水酸基、イソシアネ
ート基、カルボキシル基、グリシジル基およびアミノ基
から選ばれた少なくとも1種の官能基を有する少なくと
も1種の樹脂100重量部に対して、5〜80重量部が
好ましく、さらに好ましくは20〜60重量部である。
5重量部未満では、耐食性が向上せず、80重量部を超
えると皮膜が脆弱になり、成形時に型かじりが生じてプ
レス加工性が低下する。また、シリカは熱分解性が劣る
ため、抵抗溶接性が低下する。外面に使用する皮膜中に
は金属粉末が添加されていないので、シリカの添加量を
内面側よりも増加させることができ、外面の耐食性にも
優れたものになる。
(Silica) Silica is added by reacting silanol groups on the silica surface with the above-mentioned resin or chromate layer.
This is because an inorganic-organic composite film having high corrosion resistance is formed, the adhesion of the organic resin film on the outer surface of the tank is improved, and the corrosion resistance is improved. As the silica, those described above can be used. The addition amount of silica is preferably from 5 to 80 parts by weight based on 100 parts by weight of at least one resin having at least one kind of functional group selected from a hydroxyl group, an isocyanate group, a carboxyl group, a glycidyl group and an amino group. And more preferably 20 to 60 parts by weight.
If the amount is less than 5 parts by weight, the corrosion resistance is not improved. If the amount is more than 80 parts by weight, the film becomes brittle, and the mold is seized at the time of molding to deteriorate the press workability. In addition, since silica has poor thermal decomposability, resistance weldability decreases. Since no metal powder is added to the coating used on the outer surface, the amount of silica added can be increased compared to the inner surface, and the outer surface has excellent corrosion resistance.

【0036】以上のような潤滑性有機樹脂のガラス転移
温度は(Tg)は0〜90℃が好ましく、さらに好まし
くは0〜85℃である。この範囲を外れるとプレス加工
性が悪く、プレス加工部の耐食性も悪くなる。プレス加
工性を要求される有機被膜には、通常Tgの高いこと
(たとえば90℃以上)が要求されるが、本発明の皮膜
は、潤滑剤が皮膜から突出された構造になっているの
で、皮膜のTgをさほど高くする必要がない。またその
他の添加剤として、顔料、チクソトロピック剤、分散
剤、揺変剤、沈殿防止剤等の添加剤を皮膜中に添加する
こともできる。潤滑性有機樹脂皮膜の平均厚みは乾燥後
0.5μm〜1.5μmとすることが好ましい。膜厚が
0.5μm未満では鋼板表面の凹凸をうめきれず、耐食
性が低下する。また1.5μmを超えると耐食性の向上
効果はあるが抵抗溶接性の低下が著しい。また金属ろう
との濡れ性が著しく劣り、ろう付け性も著しく低下す
る。
The glass transition temperature (Tg) of the lubricating organic resin as described above is preferably from 0 to 90 ° C, more preferably from 0 to 85 ° C. Outside this range, the press workability is poor, and the corrosion resistance of the pressed portion is also poor. Organic coatings that require press workability are generally required to have a high Tg (for example, 90 ° C. or higher), but the coating of the present invention has a structure in which a lubricant is projected from the coating. There is no need to increase the Tg of the coating so much. Further, as other additives, additives such as a pigment, a thixotropic agent, a dispersant, a thixotropic agent, and a suspending agent can be added to the film. The average thickness of the lubricating organic resin film after drying is preferably 0.5 μm to 1.5 μm. If the film thickness is less than 0.5 μm, the irregularities on the surface of the steel sheet cannot be filled, and the corrosion resistance decreases. If it exceeds 1.5 μm, the corrosion resistance is improved, but the resistance weldability is significantly reduced. In addition, the wettability with the metal brazing is remarkably poor, and the brazing property is also remarkably reduced.

【0037】本発明の高耐食性燃料タンク用鋼板をプレ
ス加工する場合、潤滑油を塗布しなくても、プレスの難
易度に応じて潤滑油を塗布しても全く問題はなく、むし
ろ皮膜の損傷防止の観点からは潤滑油塗布が有効であ
る。この皮膜の形成方法の一例を示す。有機樹脂を有機
溶媒に溶解後、シリカを添加し、50〜150℃で30
分〜6時間反応させる。この溶液に潤滑剤、その他添加
剤を添加し、塗料を得る。塗料はロールコータ、バーコ
ータなどの公知の方法で塗布し、150〜300℃で乾
燥する。
When the steel sheet for a high corrosion resistant fuel tank according to the present invention is pressed, there is no problem even if the lubricating oil is not applied but the lubricating oil is applied according to the difficulty of the press. From the viewpoint of prevention, application of lubricating oil is effective. An example of a method for forming this film will be described. After dissolving the organic resin in the organic solvent, silica is added and the mixture is heated at 50 to 150 ° C. for 30 minutes.
Allow to react for minutes to 6 hours. A lubricant and other additives are added to this solution to obtain a paint. The paint is applied by a known method such as a roll coater or a bar coater, and dried at 150 to 300 ° C.

【0038】(実施例)以下実施例で具体的に説明す
る。板厚0.8mmの冷延鋼板(SPCC)の電解脱
脂、電解酸洗を行った後、両面に合金化溶融亜鉛めっき
(めっき中Fe10wt%)を施した(付着量は両面と
も45g/m2 )。めっき鋼板の両面にクロメート処理
液を塗布、乾燥しクロメート層を得た(付着量は金属ク
ロム換算で両面とも40mg/m2 )。さらにその両面
に塗料をロールコートし、焼き付けた。なお比較材とし
て、特公平3−25349号記載の樹脂塗料も塗布、焼
き付けた。塗料の調製方法と皮膜特性の評価方法を以下
に示す。また樹脂層の組成と評価結果を表1,2に示
す。
(Embodiment) The embodiment will be specifically described below. After electrolytic degreasing and electrolytic pickling of a cold-rolled steel plate (SPCC) having a thickness of 0.8 mm, both surfaces were subjected to galvannealing (10% by weight of Fe in the plating) (the adhesion amount was 45 g / m 2 on both surfaces). ). A chromate treatment solution was applied to both sides of the plated steel sheet and dried to obtain a chromate layer (the amount of adhesion was 40 mg / m 2 on both sides in terms of metallic chromium). The coating was roll-coated on both sides and baked. As a comparative material, a resin paint described in JP-B-3-25349 was also applied and baked. The method for preparing the paint and the method for evaluating the film properties are shown below. Tables 1 and 2 show the composition of the resin layer and the evaluation results.

【0039】(各種塗料の調製方法) (1)アミン変性エポキシ樹脂溶液(1)および金属粉
末含有潤滑性樹脂塗料の調製方法 ビスフェノールA型エポキシ樹脂2000g(エポキシ
当量=2000)にトルエン1000gを加え、窒素置
換の後に80℃まで昇温し、均一溶液とした。次にこの
溶液にジエタノールアミン52.5gを30分かけて滴
下後、1時間反応させ、アミン変性エポキシ溶液(1)
を得た。(アミン変性エポキシ樹脂の重量平均分子量1
3000、アミン付加量0.5モル)このようにして得
られたアミン変性エポキシ樹脂溶液に後述する表1に示
す金属粉末、潤滑剤、シリカ、有機ベントナイト(ベン
トン34、沈殿防止剤)、シクロヘキサン(希釈調整
用)を加えて金属粉末潤滑性樹脂塗料を調製した。
(Method of Preparing Various Paints) (1) Method of Preparing Amine-Modified Epoxy Resin Solution (1) and Lubricant Resin Paint Containing Metal Powder To 2000 g of bisphenol A type epoxy resin (epoxy equivalent = 2000), add 1000 g of toluene. After the replacement with nitrogen, the temperature was raised to 80 ° C. to obtain a uniform solution. Next, 52.5 g of diethanolamine was added dropwise to this solution over 30 minutes, and the mixture was reacted for 1 hour to obtain an amine-modified epoxy solution (1).
I got (Weight average molecular weight of amine-modified epoxy resin 1
3000, amine addition amount 0.5 mol) Metal powder, lubricant, silica, organic bentonite (Benton 34, sedimentation inhibitor), cyclohexane ( (For dilution adjustment) was added to prepare a metal powder lubricating resin paint.

【0040】(2)アミン変性エポキシ樹脂溶液(2)
および金属粉末含有潤滑性樹脂塗料の調製方法 ビスフェノールA型エポキシ樹脂1000g(エポキシ
当量=3000)にプロピレングリコールモノメチルエ
ーテルアセテート680gを加え溶解した。ついで、ビ
スフェノールF25gと塩化リチウム1gを加え、20
0℃1時間反応させ均一溶液とした。この溶液1167
gにN−メチルエタノールアミン7.5gを2時間かけ
て滴下し、さらに70℃、3時間反応させ、アミン変性
エポキシ樹脂溶液(2)を得た。(アミン変性エポキシ
樹脂の重量平均分子量20000、アミン付加量0.6
モル)このようにして得られたアミン変性エポキシ樹脂
溶液に後述する表1に示す金属粉末、潤滑剤、シリカ、
有機ベントナイト(ベントン34、沈殿防止剤)、シク
ロヘキサン(希釈調整用)を加えて金属粉末潤滑性樹脂
塗料を調製した。
(2) Amine-modified epoxy resin solution (2)
And a method for preparing a metal powder-containing lubricating resin coating material 680 g of propylene glycol monomethyl ether acetate was added to and dissolved in 1,000 g of a bisphenol A type epoxy resin (epoxy equivalent = 3000). Then, 25 g of bisphenol F and 1 g of lithium chloride were added, and
The mixture was reacted at 0 ° C. for 1 hour to obtain a homogeneous solution. This solution 1167
7.5 g of N-methylethanolamine was added dropwise to the resulting mixture over 2 hours, and the mixture was further reacted at 70 ° C. for 3 hours to obtain an amine-modified epoxy resin solution (2). (Weight average molecular weight of the amine-modified epoxy resin: 20,000, amine addition: 0.6
Mol) The thus obtained amine-modified epoxy resin solution was added to the metal powder, lubricant, silica,
Organic bentonite (Benton 34, sedimentation inhibitor) and cyclohexane (for dilution adjustment) were added to prepare a metal powder lubricating resin paint.

【0041】(3)潤滑性有機樹脂塗料(1)の調製 ポリビニルブチラール樹脂(平均重合度=300)の固
形分30%セロソルブ溶液200gにシリカを添加す
る。ついでオルトリン酸水溶液30gを徐々に滴下し、
しかるのちに混合物を90℃まで昇温し、還流下で4時
間反応させた。次に潤滑剤を添加し、潤滑性有機樹脂塗
料(1)を調製した。
(3) Preparation of Lubricant Organic Resin Coating (1) Silica is added to 200 g of a 30% solids cellosolve solution of polyvinyl butyral resin (average degree of polymerization = 300). Then, 30 g of an aqueous solution of orthophosphoric acid was gradually added dropwise.
Thereafter, the mixture was heated to 90 ° C. and reacted under reflux for 4 hours. Next, a lubricant was added to prepare a lubricating organic resin paint (1).

【0042】(4)比較例の塗料の調製 上述の(1)〜(3)と同様に、ただし表1に示す種類
の樹脂を表1に示す量用いて調製した。比較例9につい
ては以下の塗料を用いた。
(4) Preparation of paint of comparative example In the same manner as in the above (1) to (3), but using a resin of the type shown in Table 1 in an amount shown in Table 1. For Comparative Example 9, the following paint was used.

【0043】(比較例9)最外層の有機樹脂皮膜とし
て、下記の組成のものを内面(12μm)、外面(12
μm)ともに形成させた。有機樹脂皮膜は、Al粉末
(フレーク状、厚さ3μm)45重量%と、ゴム変性エ
ポキシ樹脂とフェノキシ樹脂(それぞれ30重量%、7
0重量%)との混合物54重量%、ノニオン性フッ素系
界面活性剤1重量%の組成とした。ここでゴム変性エポ
キシ樹脂は、ブタジエンアクリロニトリル共重合ゴム2
5重量%とノボラック型エポキシ樹脂75重量%の混合
物である。
(Comparative Example 9) As the outermost organic resin film, one having the following composition was used for the inner surface (12 μm) and the outer surface (12 μm).
μm). The organic resin film is composed of 45% by weight of Al powder (flake, 3 μm in thickness), a rubber-modified epoxy resin and a phenoxy resin (30% by weight, 7% by weight, respectively).
0% by weight) and 1% by weight of a nonionic fluorinated surfactant. Here, the rubber-modified epoxy resin is a butadiene acrylonitrile copolymer rubber 2
It is a mixture of 5% by weight and 75% by weight of a novolak type epoxy resin.

【0044】(皮膜特性の評価方法)試作した被覆鋼板
のプレス加工性、抵抗溶接性、外面耐食性、内面耐食性
の評価を行なった。
(Evaluation Method of Film Properties) The press-workability, resistance weldability, outer surface corrosion resistance, and inner surface corrosion resistance of the prototype coated steel sheet were evaluated.

【0045】(1)プレス加工性評価法 (a)円筒成形試験による潤滑性評価 プレス条件:出光石油(株)製防錆油Z5を1g/m2
塗油して評価 ・ポンチ径と形状……33mmφ平底円筒 ・クリアランス……1mm ・プランクサイズ……種々変化 ・しわ押え荷重……4t ・絞り速度……60mm/sec 上記条件で、鋼板の外面側をダイス側に、内面側をポン
チ側にセットして、円筒成形し各サンプルの限界絞り比
(絞り抜けたサンプルのダイス径/ポンチ径のうち、最
大の値)を求め、この値で潤滑性を評価した。この値が
大きなものほどプレス加工性が良いことを示す。 (b)円筒成形試験による皮膜の耐パウダリング性評価 プレス条件:出光石油(株)製防錆油Z5を1g/m2
塗油して評価 ・ポンチ径と形状……33mmφ平底円筒 ・クリアランス……1mm ・プランクサイズ……66mm ・しわ押え荷重……4t ・絞り速度……60mm/sec 鋼板の外面側をダイス側に、内面側をポンチ側にセット
しカップ成形後の内面側の皮膜のパウダリングの程度を
目視観察し評価した。評価基準は、セロテープによる剥
離テストにおいてパウダリングが無いレベルを◎、セロ
テープによる剥離において少しパウダリングがあるが、
目視で観察できないレベルを○、少しパウダリングがあ
るレベルを△、非常にパウダリング量が多い場合を×と
した。
(1) Press workability evaluation method (a) Evaluation of lubricity by cylindrical molding test Press conditions: 1 g / m 2 of rust preventive oil Z5 manufactured by Idemitsu Oil Co., Ltd.
・ Punch diameter and shape: 33mmφ flat bottom cylinder ・ Clearance: 1mm ・ Planck size: Various changes ・ Wrinkle holding load: 4t ・ Drawing speed: 60mm / sec Under the above conditions, the outer surface of the steel sheet Is set on the die side, the inner side is set on the punch side, and the cylinder is formed. The limit drawing ratio of each sample (the maximum value of the die diameter / punch diameter of the sample that has been drawn out) is determined. Was evaluated. A larger value indicates better press workability. (B) Evaluation of powdering resistance of the film by a cylindrical molding test Press condition: 1 g / m 2 of rust preventive oil Z5 manufactured by Idemitsu Oil Co., Ltd.
Lubricate and evaluate ・ Punch diameter and shape: 33mmφ flat bottom cylinder ・ Clearance: 1mm ・ Planck size: 66mm ・ Wrinkle holding load: 4t ・ Drawing speed: 60mm / sec The outer surface of the steel plate is placed on the die side. The inner surface side was set on the punch side, and the degree of powdering of the film on the inner surface side after cup molding was visually observed and evaluated. The evaluation criteria are: ◎ level without powdering in the peeling test with cellophane tape, there is a little powdering in peeling with cellophane tape,
The level not visually observable was rated as ○, the level with slight powdering was rated as Δ, and the case where the amount of powdering was extremely large was rated as ×.

【0046】(2)抵抗溶接性評価法 シーム溶接条件 ・電極……クロム−銅合金、台形電極(先端R:15m
mφ) ・溶接方法……二重かさね、ラップシーム溶接 ・加圧力……400kg ・通電時間……2サイクルon、1サイクルoff(2
/50秒通電、1/50秒無通電) ・冷却……内部、外部水冷 ・溶接スピード……2.5m/min ・溶接電流……種々変化 上記の条件下で内面同士の溶接を行いTピール引っ張り
試験による母材破断の有無やナゲットラップの程度から
適正な溶接電流(kA)の範囲を求め、シーム溶接性を
評価した。
(2) Resistance Weldability Evaluation Method Seam Welding Conditions Electrode: Chromium-copper alloy, trapezoidal electrode (tip R: 15 m)
mφ) ・ Welding method ・ ・ ・ Double cap, lap seam welding ・ Pressure force ・ ・ ・ ・ ・ ・ 400kg ・ Electrification time ・ ・ ・ ・ ・ ・ 2 cycles on, 1 cycle off (2
・ Cooling: Internal / external water cooling ・ Welding speed: 2.5 m / min ・ Welding current: Various changes Weld the inner surfaces under the above conditions and T peel. An appropriate range of welding current (kA) was determined from the presence or absence of base material breakage in the tensile test and the degree of nugget wrap, and seam weldability was evaluated.

【0047】(3)外面耐食性評価法 外面に大日本塗料(株)製上塗り塗料エマロンを乾燥膜
厚10μmとなるように塗布し、120℃の炉中で20
分間焼き付けた後、JASO(塩水噴霧2時間・60
℃、20〜30RH%乾燥4時間・50℃、98RH%
2時間)条件にて平面部は300サイクル、その他は1
00サイクルのCCT試験に供し平面部、平面部クロス
カットしたものおよび(1)(b)の条件で成形したプ
レス加工品側壁部の残留板量(mm)で評価した。な
お、試験前板厚は1.0mmである。
(3) Evaluation method of outer surface corrosion resistance A top coat paint Emaron manufactured by Dainippon Paint Co., Ltd. was applied to the outer surface so as to have a dry film thickness of 10 μm, and the coating was applied in an oven at 120 ° C. for 20 minutes.
After baking for minutes, JASO (salt spray 2 hours, 60 hours)
℃, 20-30RH% drying 4 hours ・ 50 ℃, 98RH%
2 hours) 300 cycles for the flat part and 1 for the others
It was subjected to a CCT test of 00 cycles, and evaluated by the residual plate amount (mm) of the flat portion, the cross cut portion of the flat portion, and the side wall portion of the pressed product formed under the conditions (1) and (b). The thickness before the test was 1.0 mm.

【0048】(4)内面耐食性評価法 平面部および1(b)の条件で成形した平底円筒カップ
内面を評価した。平面部を評価する場合は20mm×1
00mmの試験片を準備し、無鉛ガソリン/500pp
m蟻酸水溶液=1/1(重量)の燃料中に前記試験片を
80mm浸漬し、常温で1ケ月の浸漬試験を行った後、
発錆度を面積率(%)で評価した。平底円筒カップ内面
を評価する際には33mmφ、高さ30mmに成形して
試験片とし、前記の燃料をカップ内容積の80%投入
し、常温で1ケ月の浸漬を行った後カップ内面の発錆度
を面積率(%)で評価した。前記燃料は比重の順列から
下層に蟻酸水溶液、上層に無鉛ガソリンと分離するの
で、それぞれの部位における錆発生面積率で評価した。
(4) Evaluation Method of Inner Surface Corrosion Resistance The flat surface and the inner surface of a flat-bottomed cylindrical cup molded under the conditions of 1 (b) were evaluated. 20 mm x 1 when evaluating a flat part
Prepare a test piece of 00mm and use unleaded gasoline / 500pp
The test piece was immersed in a fuel of an aqueous solution of formic acid = 1/1 (weight) by 80 mm and subjected to a one month immersion test at room temperature.
The degree of rusting was evaluated in terms of area ratio (%). When evaluating the inner surface of the flat-bottomed cylindrical cup, it was molded into a test piece having a diameter of 33 mm and a height of 30 mm. The above-mentioned fuel was charged at 80% of the inner volume of the cup, immersed for one month at room temperature, and then the inner surface of the cup was released. The degree of rust was evaluated in terms of area ratio (%). Since the fuel is separated from the formic acid aqueous solution in the lower layer and the unleaded gasoline in the upper layer from the order of the specific gravity, the rust generation area ratio at each site was evaluated.

【0049】[0049]

【表1】 [Table 1]

【0050】[0050]

【表2】 [Table 2]

【0051】表1−1 注) F123 :粒状Ni粉末、平均粒径5μm(福田金属
箔粉、カーボニルNi123) F287 :粒状Ni粉末、平均粒径2μm(福田金属
箔粉、カーボニルNi287) F123* :F123をγ−グリシドキシプロピルトリ
メトキシシランで表面処理 PE :ポリエチレンワックス 平均粒径1μm、
軟化点120℃ PE :ポリエチレンワックス 平均粒径5μm、
軟化点120℃ PTFE :ポリテトラフルオロエチレンワックス 平
均粒径2μm、軟化点125℃ S :オルガノシルカゾル 平均一次粒径10n
m S :コロイダルシリカ(日産化学スノーテック
スO)平均一次粒径10〜20nm エポキシ :重量平均分子量13000、エポキシ当量
2000、アミン化合物変性なし
Table 1-1 Note) F123: Granular Ni powder, average particle size 5 μm (Fukuda metal foil powder, Carbonyl Ni123) F287: Granular Ni powder, average particle size 2 μm (Fukuda metal foil powder, Carbonyl Ni287) F123 * : Surface treatment of F123 with γ-glycidoxypropyltrimethoxysilane PE: polyethylene wax Average particle size 1 μm,
Softening point 120 ° C PE: polyethylene wax Average particle size 5 μm,
Softening point: 120 ° C. PTFE: polytetrafluoroethylene wax Average particle size: 2 μm, softening point: 125 ° C. S: Organosilkasol Average primary particle size: 10 n
m S: Colloidal silica (Nissan Chemical Snowtex O) average primary particle size 10 to 20 nm Epoxy: Weight average molecular weight 13,000, epoxy equivalent 2000, no modification with amine compound

【0052】 [0052]

【0053】 [0053]

【0054】 [0054]

【0055】[0055]

【発明の効果】本発明の鋼板は、表裏で有機被膜組成を
違え、一方の面には、アミン変性エポキシ樹脂、潤滑
剤、特定形状のNi粉末、シリカが含有された樹脂層、
他方の面には、水酸基、イソシアネート基、カルボキシ
ル基、グリシジル基およびアミノ基から選ばれた少なく
とも1種の官能基を有する少なくとも1種の樹脂とシリ
カと潤滑剤を主成分とする樹脂層を用いることにより、
優れた内面耐食性、外面耐食性、プレス加工性、抵抗溶
接性を有する。したがって、本発明の鋼板はアルコール
およびアルコール混合ガソリン用鋼板として特に有用で
ある。
The steel sheet of the present invention has a different organic coating composition on the front and back, and has a resin layer containing an amine-modified epoxy resin, a lubricant, a Ni powder of a specific shape, and silica on one surface.
On the other surface, at least one resin having at least one functional group selected from a hydroxyl group, an isocyanate group, a carboxyl group, a glycidyl group and an amino group, and a resin layer mainly composed of silica and a lubricant are used. By doing
It has excellent inner corrosion resistance, outer corrosion resistance, press workability, and resistance weldability. Therefore, the steel sheet of the present invention is particularly useful as a steel sheet for alcohol and alcohol-blended gasoline.

【図面の簡単な説明】[Brief description of the drawings]

【図1】 本発明の高耐食性燃料タンク用鋼板を説明す
る断面図である。
FIG. 1 is a cross-sectional view illustrating a steel plate for a highly corrosion-resistant fuel tank according to the present invention.

【符号の説明】[Explanation of symbols]

1 鋼板 2 金属めっき層 3 クロメート層 4 金属粉末含有潤滑性有機樹脂層 5 潤滑性有機樹脂層 Reference Signs List 1 steel plate 2 metal plating layer 3 chromate layer 4 metal powder-containing lubricating organic resin layer 5 lubricating organic resin layer

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI B05D 7/24 303 B05D 7/24 303B C23C 28/00 C23C 28/00 C (72)発明者 尾形 浩行 千葉県千葉市中央区川崎町1番地 川崎製 鉄株式会社技術研究所内 (72)発明者 望月 一雄 千葉県千葉市中央区川崎町1番地 川崎製 鉄株式会社技術研究所内 (72)発明者 田辺 弘往 栃木県那須郡西那須野町朝日町8−15 (72)発明者 小川 修 栃木県黒磯市上厚崎690−109────────────────────────────────────────────────── ─── Continued on the front page (51) Int.Cl. 6 Identification code FI B05D 7/24 303 B05D 7/24 303B C23C 28/00 C23C 28/00 C (72) Inventor Hiroyuki Ogata Chuo-ku, Chiba-shi, Chiba No. 1 Kawasaki-cho, Kawasaki Steel Engineering Co., Ltd. (72) Kazuo Mochizuki, Inventor Kazuo Mochizuki 1, Kawasaki-cho, Chuo-ku, Chiba-shi, Chiba Prefecture Kawasaki Steel Co., Ltd. 8-15 Asahi-cho, Nasuno-cho (72) Inventor Osamu Ogawa 690-109 Kamisatsuzaki, Kuroiso City, Tochigi Prefecture

Claims (5)

【特許請求の範囲】[Claims] 【請求項1】鋼板の両表面に最下層としてZnまたはZ
nを主成分とする金属めっき層を有し、その両方の上層
にクロメート層を有し、 さらにその一方の面の上層にアミン変性エポキシ樹脂
と、粒状Ni粉末と潤滑剤とシリカとを主成分とする金
属粉末含有潤滑性有機樹脂層を有し、 かつ他方の面の上層に水酸基、イソシアネート基、カル
ボキシル基、グリシジル基およびアミノ基から選ばれた
少なくとも1種の官能基を有する少なくとも1種の樹脂
と、潤滑剤と、シリカとを主成分とする潤滑性有機樹脂
層を有することを特徴とする高耐食性燃料タンク用鋼
板。
(1) Zn or Z as a lowermost layer on both surfaces of a steel sheet.
It has a metal plating layer containing n as a main component, has a chromate layer on both upper layers, and further contains an amine-modified epoxy resin, a granular Ni powder, a lubricant, and silica on the upper layer on one side. And at least one functional group having at least one functional group selected from a hydroxyl group, an isocyanate group, a carboxyl group, a glycidyl group and an amino group in the upper layer on the other surface. A highly corrosion-resistant steel plate for a fuel tank, comprising a lubricating organic resin layer containing a resin, a lubricant, and silica as main components.
【請求項2】前記金属粉末含有潤滑性有機樹脂層が、ア
ミン変性エポキシ樹脂100重量部に対して、粒状Ni
粉末が20〜400重量部、潤滑剤が0.1〜5重量
部、シリカが40重量部以下であることを特徴とする請
求項1に記載の高耐食性燃料タンク用鋼板。
2. The method according to claim 1, wherein the metal powder-containing lubricating organic resin layer is formed of a particulate Ni based on 100 parts by weight of the amine-modified epoxy resin.
The steel plate for a highly corrosion resistant fuel tank according to claim 1, wherein the powder is 20 to 400 parts by weight, the lubricant is 0.1 to 5 parts by weight, and the silica is 40 parts by weight or less.
【請求項3】前記アミン変性エポキシ樹脂が、エポキシ
基1当量に対し、0.3〜1.0モルのアミン化合物を
付加してなる複合体樹脂であり、かつ重量平均分子量が
5000〜50000の範囲であり、 前記粒状Ni粉末が平均粒径1〜9μmであり、 前記潤滑剤が、ポリオレフィンワックスおよび/または
ポリテトラフルオロエチレンであり、平均粒径1〜10
μmであり、軟化点が70〜150℃であることを特徴
とする請求項1または2に記載の高耐食性燃料タンク用
鋼板。
3. The amine-modified epoxy resin is a composite resin obtained by adding 0.3 to 1.0 mol of an amine compound to 1 equivalent of an epoxy group, and has a weight average molecular weight of 5,000 to 50,000. Wherein the granular Ni powder has an average particle size of 1 to 9 μm, the lubricant is a polyolefin wax and / or polytetrafluoroethylene, and the average particle size is 1 to 10 μm.
3. The steel sheet for a highly corrosion-resistant fuel tank according to claim 1, wherein the steel sheet has a softening point of 70 to 150 ° C.
【請求項4】前記潤滑性有機樹脂層が、前記樹脂100
重量部に対して、潤滑剤が1〜40重量部と、シリカが
5〜80重量部である請求項1〜3のいずれかに記載の
高耐食性燃料タンク用鋼板。
4. The method according to claim 1, wherein the lubricating organic resin layer comprises
The highly corrosion-resistant fuel tank steel plate according to any one of claims 1 to 3, wherein the lubricant is 1 to 40 parts by weight and the silica is 5 to 80 parts by weight based on parts by weight.
【請求項5】前記潤滑性有機樹脂層中の潤滑剤がポリオ
レフィンワックスおよび/またはポリテトラフルオロエ
チレンであり、該潤滑剤の軟化点が70〜150℃、か
つ平均粒径が1〜7μmであり、 該潤滑性有機樹脂のガラス転移温度(Tg)が0〜90
℃である請求項1〜4のいずれかに記載の高耐食性燃料
タンク用鋼板。
5. The lubricant in the lubricating organic resin layer is a polyolefin wax and / or polytetrafluoroethylene, wherein the lubricant has a softening point of 70 to 150 ° C. and an average particle size of 1 to 7 μm. The glass transition temperature (Tg) of the lubricating organic resin is from 0 to 90.
The steel sheet for a highly corrosion-resistant fuel tank according to any one of claims 1 to 4, which has a temperature of ℃.
JP32142397A 1997-11-21 1997-11-21 Steel plate for high corrosion resistant fuel tank Expired - Lifetime JP3934763B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP32142397A JP3934763B2 (en) 1997-11-21 1997-11-21 Steel plate for high corrosion resistant fuel tank

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP32142397A JP3934763B2 (en) 1997-11-21 1997-11-21 Steel plate for high corrosion resistant fuel tank

Publications (2)

Publication Number Publication Date
JPH11151777A true JPH11151777A (en) 1999-06-08
JP3934763B2 JP3934763B2 (en) 2007-06-20

Family

ID=18132394

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JP3934763B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008201053A (en) * 2007-02-21 2008-09-04 Nippon Steel Corp Surface-treated metal plate

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008201053A (en) * 2007-02-21 2008-09-04 Nippon Steel Corp Surface-treated metal plate

Also Published As

Publication number Publication date
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