JPH02270998A - Composite electroplated steel sheet having high corrosion resistance - Google Patents
Composite electroplated steel sheet having high corrosion resistanceInfo
- Publication number
- JPH02270998A JPH02270998A JP2061148A JP6114890A JPH02270998A JP H02270998 A JPH02270998 A JP H02270998A JP 2061148 A JP2061148 A JP 2061148A JP 6114890 A JP6114890 A JP 6114890A JP H02270998 A JPH02270998 A JP H02270998A
- Authority
- JP
- Japan
- Prior art keywords
- steel sheet
- corrosion resistance
- electroplated steel
- cationic polymer
- composite electroplated
- 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
Links
- 230000007797 corrosion Effects 0.000 title claims abstract description 43
- 238000005260 corrosion Methods 0.000 title claims abstract description 43
- 229910000831 Steel Inorganic materials 0.000 title claims abstract description 33
- 239000010959 steel Substances 0.000 title claims abstract description 33
- 239000002131 composite material Substances 0.000 title claims abstract description 26
- 238000007747 plating Methods 0.000 claims abstract description 36
- 229920006317 cationic polymer Polymers 0.000 claims abstract description 22
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 18
- 229920000642 polymer Polymers 0.000 claims abstract description 13
- 229910052804 chromium Inorganic materials 0.000 claims abstract description 7
- 238000009713 electroplating Methods 0.000 claims abstract description 7
- 229910052750 molybdenum Inorganic materials 0.000 claims abstract description 4
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 4
- 229910052721 tungsten Inorganic materials 0.000 claims abstract description 4
- 229910052726 zirconium Inorganic materials 0.000 claims abstract description 4
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 3
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 3
- 239000010419 fine particle Substances 0.000 claims description 17
- 229910045601 alloy Inorganic materials 0.000 claims description 7
- 239000000956 alloy Substances 0.000 claims description 7
- 125000003277 amino group Chemical group 0.000 claims description 2
- 239000010410 layer Substances 0.000 abstract description 21
- 239000002245 particle Substances 0.000 abstract description 8
- 150000001412 amines Chemical class 0.000 abstract description 6
- 239000002356 single layer Substances 0.000 abstract description 2
- 230000001105 regulatory effect Effects 0.000 abstract 2
- PUAQLLVFLMYYJJ-UHFFFAOYSA-N 2-aminopropiophenone Chemical compound CC(N)C(=O)C1=CC=CC=C1 PUAQLLVFLMYYJJ-UHFFFAOYSA-N 0.000 abstract 1
- 229910001297 Zn alloy Inorganic materials 0.000 abstract 1
- 239000011701 zinc Substances 0.000 description 22
- 230000000694 effects Effects 0.000 description 11
- -1 Cr3+ ions Chemical class 0.000 description 7
- 150000002500 ions Chemical class 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- 229920000768 polyamine Polymers 0.000 description 6
- 230000001681 protective effect Effects 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical group [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 238000001556 precipitation Methods 0.000 description 4
- 229910001335 Galvanized steel Inorganic materials 0.000 description 3
- 150000001450 anions Chemical class 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 239000008397 galvanized steel Substances 0.000 description 3
- 238000000227 grinding Methods 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 238000003466 welding Methods 0.000 description 3
- VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical compound NCC=C VVJKKWFAADXIJK-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 229910007567 Zn-Ni Inorganic materials 0.000 description 2
- 229910007614 Zn—Ni Inorganic materials 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000004566 building material Substances 0.000 description 2
- 239000010960 cold rolled steel Substances 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 150000003457 sulfones Chemical class 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 229910052695 Americium Inorganic materials 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- 238000001479 atomic absorption spectroscopy Methods 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000010953 base metal Substances 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000009841 combustion method Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000004070 electrodeposition Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000004313 glare Effects 0.000 description 1
- 229910052745 lead Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 229910052752 metalloid Inorganic materials 0.000 description 1
- 150000002738 metalloids Chemical class 0.000 description 1
- DYUWTXWIYMHBQS-UHFFFAOYSA-N n-prop-2-enylprop-2-en-1-amine Chemical compound C=CCNCC=C DYUWTXWIYMHBQS-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001174 sulfone group Chemical group 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
Landscapes
- Electroplating Methods And Accessories (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は自動車、家電、建材等に使用される耐食性、お
よび加工性に優れた防錆用の複合電気めっき鋼板に関す
る。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a composite electroplated steel sheet for rust prevention that has excellent corrosion resistance and workability and is used in automobiles, home appliances, building materials, etc.
(従来の技術)
冷延鋼板の加工性や強度を損なわずに量産化できる高耐
食性鋼板として電気亜鉛めっき鋼板が汎用されているこ
とは周知である。(Prior Art) It is well known that electrogalvanized steel sheets are widely used as highly corrosion-resistant steel sheets that can be mass-produced without impairing the workability or strength of cold-rolled steel sheets.
近年では寒冷地帯における冬期の道路凍結防止用の散布
塩に対する自動車の防錆鋼板として亜鉛めっき鋼板の使
用が試みられ、苛酷な腐食環境での耐食性の要求が増加
する傾向にある。In recent years, attempts have been made to use galvanized steel sheets as anti-corrosive steel sheets for automobiles in response to salt sprayed to prevent roads from freezing during the winter in cold regions, and there is an increasing trend in the demand for corrosion resistance in harsh corrosive environments.
これら亜鉛めっき鋼板の耐食性の向上要求に対して亜鉛
のめっき量(付着量)による耐食性の向上が知られてい
るが、めっき量の増加以外の方法として亜鉛自身の溶解
を抑制するための合金めっきが数多く提案されている。In response to these demands for improving the corrosion resistance of galvanized steel sheets, it is known that corrosion resistance can be improved by increasing the amount of zinc plating (adhesion amount). Many have been proposed.
これらの多くは、Fe、Ni、Coといった鉄族元素を
合金成分として含有するものであり、未塗装あるいは塗
装後の耐食性が亜鉛めっき鋼板に比べて優れる特徴があ
リ、工業的に生産、実用化されているが、耐食性を更に
向上させることが強く望まれている。Many of these contain iron group elements such as Fe, Ni, and Co as alloying components, and have superior corrosion resistance after unpainted or painted compared to galvanized steel sheets, making them difficult to produce industrially and put into practical use. However, it is strongly desired to further improve corrosion resistance.
一方、 ZnないしZn系合金めっき中にCrを含有さ
せた電気めっき鋼板として、例えば特公昭59−383
13及び59−40234号公報。On the other hand, as an electroplated steel sheet containing Cr in Zn or Zn-based alloy plating, for example, Japanese Patent Publication No. 59-383
13 and 59-40234.
特開昭61−130498.61−270398゜62
−54099号公報等が開示されている。JP-A-61-130498.61-270398゜62
-54099 etc. are disclosed.
これらは何れもCr含有率は微量であって、耐食性にと
ってCrの効果は付随的でしかあり得ない。All of these have a trace amount of Cr content, and the effect of Cr on corrosion resistance can only be incidental.
(発明が解決しようとする課M)
しかしながら、従来Cr含有率を高め得るZn−Cr電
気めっき技術がなかった。即ち、単にめっき浴中の3価
Crイオン濃度を高めても加工性の良い正常なめっきが
得られず、電流効率も急減する等の障害があって工業的
にCr含有率の高い電気めっき鋼板を得ることは極めて
困難であった。(Problem M to be solved by the invention) However, conventionally there has been no Zn-Cr electroplating technology capable of increasing the Cr content. In other words, even if the concentration of trivalent Cr ions in the plating bath is simply increased, normal plating with good workability cannot be obtained, and there are problems such as a sudden decrease in current efficiency, so that electroplated steel sheets with high Cr content cannot be manufactured industrially. It was extremely difficult to obtain.
本発明は、上記問題点に鑑み、従来にない高Cr含有率
の耐食性及び加工性に優れた実用性の高いZn−Cr系
の複合電気めっき鋼板を提供するものである。In view of the above problems, the present invention provides a highly practical Zn-Cr composite electroplated steel sheet with an unprecedented high Cr content, excellent corrosion resistance and workability.
(課題を解決するための手段)
本発明は、Z n2” 、 Cr3+イオンと酸化物微
粒子を含むめっき浴に水溶性のカチオンポリマーを導入
し、 この作用でCr析出を促進することにより、従来
にない高Cr含有率のZn−Cr系複合電気めっきを得
ることができ、かつ、カチオンポリマーの微量共析によ
り加工性も確保することに成功したものである。また、
酸化物微粒子の含有によりCrの耐食性に対する効果を
更に向上させたものである。(Means for Solving the Problems) The present invention introduces a water-soluble cationic polymer into a plating bath containing Zn2'', Cr3+ ions and oxide fine particles, and this action promotes Cr precipitation, thereby improving the conventional method. It was possible to obtain a Zn-Cr-based composite electroplating with a high Cr content, and also to ensure workability by eutectoiding a small amount of cationic polymer.Also,
The effect of Cr on corrosion resistance is further improved by containing oxide fine particles.
本発明の要旨は鋼板の表面に、 Cr1〜30重量%、
酸化物微粒子0.1〜10重量%、カチオンポリマー0
.001〜5重景%、残部Znとする複合電気めっき層
を形成したことを特徴とする高耐食性複合電気めっき鋼
板、
上層にZnもしくはZn系合金めっき層を形成したこと
を特徴とする上記高耐食性複合電気めっき鋼板、
酸化物微粒子が、Si、Al、Zr、Ti、Cr。The gist of the present invention is that 1 to 30% by weight of Cr is added to the surface of the steel plate.
Oxide fine particles 0.1-10% by weight, cationic polymer 0
.. A highly corrosion-resistant composite electroplated steel sheet characterized by forming a composite electroplated layer containing 001 to 5% Zn and the balance Zn; Composite electroplated steel sheet, oxide fine particles are Si, Al, Zr, Ti, Cr.
Mo、Wの酸化物の1種以上からなる上記高耐食性複合
電気めっき鋼板、
カチオンポリマーが、4級アミンポリマーである上記高
耐食性複合電気めっき鋼板である。The above-mentioned highly corrosion-resistant composite electroplated steel sheet is made of one or more types of oxides of Mo and W. The above-mentioned highly corrosion-resistant composite electroplated steel sheet is such that the cationic polymer is a quaternary amine polymer.
(作用)
本発明者らは、従来になくCr含有率の高いZn−Cr
系複合電気めっき鋼板の製造方法を開発し。(Function) The present inventors have discovered that Zn-Cr has a higher Cr content than ever before.
Developed a method for manufacturing composite electroplated steel sheets.
耐食性を画期的に向上させる目途を得た。更に研究を続
けたところ、長期の曝露テストを行なうと耐食性向上の
ためには、まだ改善の余地があることが判明した。すな
わち、CrはZnとの共存下では不働態化せず、 Zn
とともに犠牲防食作用に加担し、 しかもCrの腐食生
成物が難溶性の保護皮膜を沈積する。これにより腐食を
抑制していることが高耐食性を発揮する理由であろうと
考えられが、実際に使用される状態に近い曝露環境下で
は、乾燥時間が長いため、 Crの腐食生成物からな
る難溶性の保護皮膜に亀裂が発生しやすい。このため、
ある時間が経過すると、急激に腐食が進行してしまう。We have found a way to dramatically improve corrosion resistance. Further research and long-term exposure tests revealed that there was still room for improvement in improving corrosion resistance. In other words, Cr does not become passivated in the coexistence with Zn, and Zn
In addition, the corrosion products of Cr deposit a poorly soluble protective film. It is thought that this suppresses corrosion and is the reason for its high corrosion resistance.However, under an exposure environment close to the actual usage conditions, the drying time is long, so the corrosion caused by corrosion products of Cr is difficult to maintain. Cracks are likely to occur in the soluble protective film. For this reason,
After a certain period of time, corrosion progresses rapidly.
この欠点を補う方法として、酸化物微粒子をめっき層中
に共析させることが有効であることを見出したのである
。酸化物微粒子はZnやCrの腐食生成物中に入りこん
で、これと強く結合し、また吸湿性を有するために、乾
燥状態になっても、腐食生成物の保護皮膜にひずみが入
りにくく、その結果保護皮膜の″亀裂発生が抑制される
と考えられる。このように、酸化物微粒子を含有゛させ
ることにより、Zn−Cr系複合めっきの保護皮膜的な
腐食生成物を更に安定化することができる。The inventors have found that eutectoiding oxide fine particles into the plating layer is effective as a method to compensate for this drawback. Oxide fine particles penetrate into Zn and Cr corrosion products and bond strongly with them, and because they have hygroscopic properties, even in dry conditions, they do not easily strain the protective film of the corrosion products. As a result, it is thought that the occurrence of cracks in the protective film is suppressed.In this way, by containing oxide fine particles, it is possible to further stabilize the corrosion products of the protective film of Zn-Cr composite plating. can.
以下1本発明の詳細な説明する。The present invention will be explained in detail below.
本発明の複合電気めっき鋼板の耐食性は、主としてCr
の作用である。Cr含有率は、1〜30重量%とする。The corrosion resistance of the composite electroplated steel sheet of the present invention is mainly due to Cr.
This is the effect of The Cr content is 1 to 30% by weight.
1重量%未満では、耐食性向上に有効ではない。5重量
%以上になると、例えば塩水噴霧試験等では赤錆発生が
抑制され1画期的な効果が表われてくる。If it is less than 1% by weight, it is not effective in improving corrosion resistance. When the amount is 5% by weight or more, the generation of red rust is suppressed in, for example, a salt spray test, and an epoch-making effect appears.
このような高耐食性は、従来公知のZnめっきあるいは
Zn−Fe、Zn−Ni等の合金めっきでは到底達成す
ることはできない。Such high corrosion resistance cannot be achieved by conventionally known Zn plating or alloy plating such as Zn-Fe or Zn-Ni.
Cr含有率が30重量%を超えると、耐食性は良いもの
の、後述するカチオンポリマーの共析による作用をもっ
てしても、プレス加工等の加工時にめっき層が剥離する
いわゆるパウダリング性の劣化を防止し得ず、実用上は
適用が難しい。When the Cr content exceeds 30% by weight, corrosion resistance is good, but even with the effect of the eutectoid of the cationic polymer described below, deterioration of so-called powdering property, in which the plating layer peels off during processing such as press working, cannot be prevented. However, it is difficult to apply in practice.
耐食性及び加工性の点からは、 Cr含有率は5〜20
重量%がより好ましい。From the viewpoint of corrosion resistance and workability, the Cr content is 5 to 20.
% by weight is more preferred.
酸化物微粒子の含有率は、 0.1〜10重量%とする
。0.1重量%未満では、前述した腐食生成物の安定化
に対する作用が小さく効果的ではない、10重量%超で
は加工性が著しく劣化してしまう、加工性の観点からは
、 0.1〜5重量%がより好ましい、酸化物微粒子の
種類としては、半金属や金属の酸化物等積々あるが、S
i、 A Q 。The content of oxide fine particles is 0.1 to 10% by weight. If it is less than 0.1% by weight, the effect on stabilizing the corrosion products described above will be small and it will not be effective. If it exceeds 10% by weight, the workability will be significantly deteriorated. From the viewpoint of workability, from 0.1 to There are many types of oxide fine particles, which are more preferably 5% by weight, such as metalloid and metal oxides, but S
i, AQ.
Zr、Ti、Cr、Mo、Wの酸化物が特に好ましく、
これらを、1種もしくは2種以上混合して用いてもよい
、酸化物微粒子の大きさは、平均粒径として1μ−以下
が好ましく、1μ園超のものでは、めっき層中に共析し
難い。Oxides of Zr, Ti, Cr, Mo, and W are particularly preferred;
These may be used alone or in a mixture of two or more.The size of the oxide fine particles is preferably 1μ or less as an average particle diameter, and if it exceeds 1μ, it is difficult to eutectoid in the plating layer. .
カチオンポリマーは、Crの析出促進剤であり、かつC
rと共に微量めっき層内に共析することにより、加工時
の耐パウダリング性を向上させる。The cationic polymer is a precipitation accelerator for Cr and
By eutectoiding with r in a small amount within the plating layer, powdering resistance during processing is improved.
このようなカチオンポリマーの共析効果は、Crイオン
がZnや鉄族金属の均一な電析成長を阻害し、均一性、
平滑性に欠けためっき構造となってしまうことを防止す
る点にあると推定される。即ち、共析したカチオンポリ
マーを介することによってZnや鉄族金属とCrが均一
に混合もしくは合金化した緻密なめっき層が形成される
と考えられる。カチオンポリマーの含有率としては、0
.001〜5重量%とする。O,OQ1重量%未満では
、加工時の耐パウダリング性に対して効果が乏しく、ま
た5重量%超の含有率は、めっき浴中のカチオンポリマ
ー濃度を増しても得られ難いのみならず多量に共析する
とめっき密着性が低下する原因となる。加工性の観点か
らは、 Cr含有率の1/1000以上の含有率でカチ
オンポリマーを共析させるとよい。This eutectoid effect of cationic polymers is due to the fact that Cr ions inhibit the uniform deposition growth of Zn and iron group metals, resulting in uniformity and
It is presumed that the purpose is to prevent a plating structure lacking in smoothness. That is, it is thought that a dense plating layer in which Zn or iron group metals and Cr are uniformly mixed or alloyed is formed through the eutectoid cationic polymer. The content of cationic polymer is 0
.. 001 to 5% by weight. If the O,OQ content is less than 1% by weight, the effect on powdering resistance during processing is poor, and if the content exceeds 5% by weight, it is not only difficult to obtain even if the cationic polymer concentration in the plating bath is increased, but also a large amount If eutectoid is used, it will cause a decrease in plating adhesion. From the viewpoint of processability, it is preferable to eutectoid the cationic polymer at a content of 1/1000 or more of the Cr content.
本発明に用いる水溶性のカチオンポリマーは4級アミン
の重合物が効果的なポリマーであり、分子量は、この場
合、10’〜10”が望ましい。次ぎに示すアミンポリ
マーの内、ポリアミンスルホン(PASと略)およびポ
リアミン(P A)がCr析出促進剤として最も効果的
である。アミン基による吸着作用とスルホン基と金属イ
オンもしくは金属の結合が寄与していると考えられる6
基本的には、次に示す4級アミンの塩(アンモニウム塩
)
あるいはコポリマーで構成されている。The water-soluble cationic polymer used in the present invention is effectively a quaternary amine polymer, and the molecular weight is preferably 10' to 10'' in this case. Among the following amine polymers, polyamine sulfone (PAS) ) and polyamine (PA) are the most effective as Cr precipitation promoters.It is thought that the adsorption effect of the amine group and the bond between the sulfone group and the metal ion or metal contribute6.
Basically, it is composed of the following quaternary amine salts (ammonium salts) or copolymers.
以下具体的にいくつかの化合物を列挙する。Some specific compounds are listed below.
ジアリルアミンから得られる高分子があげられる。R1
,R2はアルキル基を示し、
N ・・・・・X
/ \
1R2
CH。Examples include polymers obtained from diallylamine. R1
, R2 represents an alkyl group, N...X/\1R2CH.
N ・・・・・X
XはCQ−、H3O4−、H,PO4−、R−8O3−
(RはC工〜C4のアルキル基)、No、−のアニオン
を示す。N...X X is CQ-, H3O4-, H, PO4-, R-8O3-
(R is a C-C4 alkyl group), No, and an anion of -.
あるいはビニルベンジルから合成される高分子があげら
れる。R□、R,、R,は炭化水素を示し、千CH2−
CH+1
CI+□
XはCα−、HSO4−、H2PO,−、R−8O,−
。Another example is a polymer synthesized from vinylbenzyl. R□, R,, R, represents a hydrocarbon, and 1,000 CH2-
CH+1 CI+□ X is Cα-, HSO4-, H2PO,-, R-8O,-
.
No、−のアニオンを示す。No, indicates an anion of -.
あるいはアリルアミンポリマーがあげられる。Alternatively, allylamine polymer can be mentioned.
千C1+、 −CH−9 N・・・X 4PARと略す。Thousand C1+, -CH-9 N...X Abbreviated as 4PAR.
R= 、Rz −R,−は炭化水素を示し、XはCQ−
。R= , Rz -R,- represents a hydrocarbon, X is CQ-
.
HS O4−、I(SP O4−、R−S O,−、N
o、−のアニオンを示す。この他1,2.3級のアミン
のポリマーも前述の4級アミンポリマーに及ばなし)が
Cr析出促進剤として効果がある。HS O4-, I(SP O4-, R-S O,-, N
Indicates an anion of o and -. In addition, polymers of primary, secondary, and tertiary amines are also effective as Cr precipitation promoters (not as good as the above-mentioned quaternary amine polymers).
めっき付着量は、10〜50g/rdで十分耐食性を確
保できる。また、 Zn、 Cr、酸化物微粒子。A coating weight of 10 to 50 g/rd can ensure sufficient corrosion resistance. Also, Zn, Cr, oxide fine particles.
カチオンポリマー以外にもPb、 Sn、 A4. I
n。In addition to cationic polymers, Pb, Sn, A4. I
n.
Bi、Cu、Sb、Am、Na、P、S 等が不可避的
に微量共析していても本質的に本発明の効果は変わらな
いものである。Even if Bi, Cu, Sb, Am, Na, P, S, etc. inevitably eutectoid, the effects of the present invention remain essentially the same.
このようにしてなる複合電気めっき鋼板は、単層のまま
でもよいし、上層にZnもしくはZn−Ni。The composite electroplated steel sheet formed in this way may be left as a single layer, or may have Zn or Zn-Ni as an upper layer.
7、n−Fe等のZn系合金めっきを少量流してもよい
、上層に、ZnもしくはZn系合金めっきを施す場合に
は、1〜5 g/rdが望ましく、こうすることにより
、化成処理やカチオン電着性をより確実なものとし、ひ
いては塗装後耐食性を更に向上せしめる。7. A small amount of Zn-based alloy plating such as n-Fe may be applied. When Zn or Zn-based alloy plating is applied to the upper layer, 1 to 5 g/rd is desirable. By doing so, chemical conversion treatment and It makes the cationic electrodeposition more reliable and further improves the corrosion resistance after painting.
次に本発明の複合電気めっき鋼板の製造方法であるが、
Zn”+イオン、Cr’+イオン、5in2゜AQ
z03.TiO2の如き酸化物微粒子、及びPASの如
き4級アミンの重合物等の水溶性力チオンポIJ ?−
を0.01〜20gIQを含む、p)10.5〜3、浴
温40〜70℃の酸性めっき浴を用いて2OA/dr+
f以上で電気めっきすればよい。Next, the method for manufacturing a composite electroplated steel sheet of the present invention,
Zn"+ ion, Cr'+ ion, 5in2゜AQ
z03. Water-soluble polymers such as oxide fine particles such as TiO2 and polymers of quaternary amines such as PAS? −
containing 0.01 to 20 g IQ, p) 10.5 to 3, using an acidic plating bath with a bath temperature of 40 to 70°C, 2OA/dr+
Electroplating may be performed at f or higher.
更に、Na”、K”、NH4+イオン等の塩を添加する
ことは、浴の電導度を高めるために有効である。Furthermore, addition of salts such as Na", K", NH4+ ions, etc. is effective in increasing the conductivity of the bath.
上層のZnもしくはZn系合金めっきは、周知の電気め
っき法を適用することができる。その場合、下層のめっ
き浴から持ち出されるCrイオンやカチオンポリマーを
含むドラッグアウトを、上層めっき前に水洗により十分
除去することが好ましい。A well-known electroplating method can be applied to the Zn or Zn-based alloy plating on the upper layer. In that case, it is preferable to sufficiently remove drag-out containing Cr ions and cationic polymers carried out from the plating bath of the lower layer by washing with water before plating the upper layer.
本発明の構造は必ずしも鋼板の両面に対して用いる必要
はなく、用途に応じて片面のみに適用し、他の面は鋼板
のまま、もしくは他のめっき層、あるいは有機皮膜を被
覆しためっき層としてもよい。The structure of the present invention does not necessarily have to be applied to both sides of a steel plate, but can be applied to only one side depending on the application, and the other side can be used as a steel plate or as a plating layer coated with another plating layer or an organic film. Good too.
本発明を適用する素地鋼板は通常ダル仕上げ圧延をした
軟鋼板であるが、ブライト仕上げ圧延をした軟鋼板、鋼
成分としてMn、S、P等を多く含んだ高張力鋼板Cr
、Cu、Ni+ P等を多く含んだ腐食速度の小さい高
耐食性鋼板でも適用可能である。The base steel sheet to which the present invention is applied is usually a mild steel sheet that has been subjected to dull finish rolling, but it may also be a mild steel sheet that has been brightly finished rolled, or a high-strength steel sheet that contains a large amount of Mn, S, P, etc. as a steel component.
It is also applicable to highly corrosion-resistant steel plates containing a large amount of , Cu, Ni+P, etc. and having a low corrosion rate.
(実施例)
板厚0.8−の冷延鋼板を、アルカリ脱脂し、5%硫酸
で酸洗した後、水洗し、以下の条件により、電気めっき
を行なった。ポンプ撹拌により液流速9Qm/l1li
n、 極間距離1−Onyeとし、浴温60℃、pH
2の硫酸酸性浴を用いた。めっき浴組成は、Zn”+イ
オン70 g/ Q 、 Cr”イオン1〜30 g
/ Q v酸化物微粒子(’S j、0. 、 A Q
z○、。(Example) A cold-rolled steel plate with a thickness of 0.8 mm was degreased with alkali, pickled with 5% sulfuric acid, washed with water, and electroplated under the following conditions. Liquid flow rate 9Qm/l1li by pump stirring
n, interelectrode distance 1-Onye, bath temperature 60℃, pH
No. 2 sulfuric acid acid bath was used. The plating bath composition was 70 g/Q of Zn"+ ions, 1 to 30 g of Cr" ions.
/ Q v oxide fine particles ('S j, 0., A Q
z○,.
ZrO2,TiO2は、平均粒径0.02〜0.05μ
。ZrO2, TiO2 have an average particle size of 0.02 to 0.05μ
.
CrzOi)WO3は平均粒径0.1〜0.5p)を1
0〜l OOg / Q 、カチオンポリマー(分子量
1万のポリアミンポリマー(PA)、あるいは分子量1
2万のポリアミンスルホンポリマー(PAS))0.0
1〜20 g/ Q 、 Na+イオン16.IQとし
。CrzOi)WO3 has an average particle size of 0.1-0.5p)
0 to l OOg/Q, cationic polymer (polyamine polymer (PA) with a molecular weight of 10,000, or molecular weight 1
20,000 polyamine sulfone polymer (PAS)) 0.0
1-20 g/Q, Na+ ion 16. As for IQ.
各成分のめっき層中の含有率は、それぞれの添加量及び
電流密度によりコントロールし、めっき付着量は20g
’/rrfとした。また、1部については上層に、周知
の条件でZnもしくはZn系合金めっきを3g/ボ施し
た。The content of each component in the plating layer is controlled by the amount added and current density, and the amount of plating deposited is 20g.
'/rrf. Further, for one part, the upper layer was plated with 3 g/bo of Zn or Zn-based alloy under well-known conditions.
このようにして製造した複合電気めっき鋼板のめっき組
成及び評価結果を第1表に示す。なお、めっき層中のZ
n + CI7 +酸化物微粒子については原子吸光
法で分析し、カチオンポリマーについては、燃焼法によ
りC分析を行ないカチオンポリマー量に換算した。耐食
性、加工性評価方法については以下の通りである8
(1)未塗装耐食性
■塩水散布曝露試験(千葉系地区に曝露1週1回、5%
塩水を散布、曝露と略)1年間後の赤錆発生面積で評価
した。Table 1 shows the plating composition and evaluation results of the composite electroplated steel sheet manufactured in this manner. In addition, Z in the plating layer
The n + CI7 + oxide fine particles were analyzed by atomic absorption spectrometry, and the cationic polymer was analyzed by C analysis by the combustion method and converted into the amount of cationic polymer. The corrosion resistance and processability evaluation method is as follows.
Spraying salt water (abbreviated as "exposure") was evaluated based on the area where red rust occurred after one year.
1%以下:0
1%超〜10%以下:0
10%超〜30%以下:Δ
30%超 :X
(2)塗装後耐食性
浸漬型リン酸塩処理、カチオン電着塗装20μmを施こ
し、 中塗り、水研ぎ、上塗り塗装をして総合膜厚10
0μ田とし、地鉄に達するクロスカットを入れた試験片
について、塩水噴霧試験(JIS Z 2371に準拠
、SSTと略)を1000時間、及び上記曝露試験を1
年間行ない、それぞれについてクロスカット部のふくれ
巾で評価した。1% or less: 0 More than 1% to less than 10%: 0 More than 10% to less than 30%: Δ More than 30%: Intermediate coating, wet sanding, and top coating to achieve a total film thickness of 10
A test piece with a 0 μ field and a cross cut reaching the base metal was subjected to a salt spray test (according to JIS Z 2371, abbreviated as SST) for 1000 hours and the above exposure test for 1 time.
The test was carried out for a year, and each test was evaluated based on the bulge width of the cross-cut part.
11[o以下二〇 111n超〜3m以下:0 3m超〜5rrfa以下:Δ 51m超 :× (3)スポット溶接性 溶接条件は以下の通りである。11[o below 20 More than 111n to less than 3m: 0 More than 3m to less than 5rrfa: Δ Over 51m: × (3) Spot weldability The welding conditions are as follows.
電 流:8kA
サイクル数:10サイクル
加圧カニ200眩
溶接チップ形状:第1図に示す。(Aは12mφ、Bは
6omφ、0は30”
である。)
3000点連続打点を行なった後のナゲツト径を測定し
た。Current: 8 kA Number of cycles: 10 cycles Pressure crab 200 glare Welding tip shape: As shown in Figure 1. (A is 12 mφ, B is 6 omφ, and 0 is 30".) The nugget diameter after 3000 consecutive points was measured.
4m以上 :◎
3m以上〜41m未満:0
3wn未満 :X
(4)加工性
50φX25Hの円筒プレス成形を行なった後、加工面
についてテープ剥離を行ない、重量減少量で評価した。4 m or more: ◎ 3 m or more to less than 41 m: 0 Less than 3 wn:
2■以下:◎ 211g超〜5■以下:0 5IIII超〜8■以下:Δ 8■超 :X 本発明例は、比較例に比して耐食性、溶接性。2 ■ or less: ◎ Over 211g ~ 5■ or less: 0 More than 5III to less than 8■: Δ Over 8:X The present invention example has better corrosion resistance and weldability than the comparative example.
加工性共に明らかに良好である。Both workability is clearly good.
(発明の効果)
以上述べたように、本発明の複合電気めっき鋼板は、Z
n−Cr系複合めっき中に酸化物微粒子を含有させるこ
とによりCr含有めっき特有の保護皮膜的な腐食生成物
を更に安定化させることにより、特に曝露環境下での耐
食性向上を図ったものであり、溶接性、加工性にも優れ
ることから、高度な防錆性能を要求される自動車用を中
心として、家電、建材用の防錆鋼板として好適である。(Effect of the invention) As described above, the composite electroplated steel sheet of the present invention has Z
By incorporating oxide fine particles into the n-Cr composite plating, the protective film-like corrosion products peculiar to Cr-containing plating are further stabilized, thereby improving corrosion resistance, especially in exposed environments. Because of its excellent weldability and workability, it is suitable as a rust-proof steel sheet for automobiles, home appliances, and building materials, which require a high degree of rust-proofing performance.
第1図は、実施例においてスポット溶接性を評価するた
めに用いた溶接チップ形状を示す図である。
−IJ−
第1図FIG. 1 is a diagram showing a welding tip shape used to evaluate spot weldability in Examples. -IJ- Figure 1
Claims (4)
子0.1〜10重量%、カチオンポリマー0.001〜
5重量%、残部Znとする複合電気めっき層を形成した
ことを特徴とする高耐食性複合電気めっき鋼板。(1) On the surface of the steel plate, 1 to 30% by weight of Cr, 0.1 to 10% by weight of oxide fine particles, and 0.001 to 0.001% of cationic polymer.
A highly corrosion-resistant composite electroplated steel sheet characterized by forming a composite electroplating layer containing 5% by weight and the balance being Zn.
たことを特徴とする特許請求の範囲第1項記載の高耐食
性複合電気めっき鋼板。(2) A highly corrosion-resistant composite electroplated steel sheet according to claim 1, characterized in that a Zn or Zn-based alloy plating layer is formed on the upper layer.
、Mo、Wの酸化物の1種以上からなる特許請求の範囲
第1項、第2項記載の高耐食性複合電気めっき鋼板。(3) Oxide fine particles are Si, Al, Zr, Ti, Cr
The highly corrosion-resistant composite electroplated steel sheet according to claims 1 and 2, comprising one or more of oxides of , Mo, and W.
特許請求の範囲第1項、第2項記載の高耐食性複合電気
めっき鋼板。(4) The highly corrosion-resistant composite electroplated steel sheet according to claims 1 and 2, wherein the cationic polymer is a quaternary amine polymer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2061148A JPH02270998A (en) | 1990-03-14 | 1990-03-14 | Composite electroplated steel sheet having high corrosion resistance |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2061148A JPH02270998A (en) | 1990-03-14 | 1990-03-14 | Composite electroplated steel sheet having high corrosion resistance |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP23226588A Division JPH0280597A (en) | 1988-05-17 | 1988-09-19 | Composite electroplated steel sheet having high corrosion resistance |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02270998A true JPH02270998A (en) | 1990-11-06 |
JPH0534436B2 JPH0534436B2 (en) | 1993-05-24 |
Family
ID=13162739
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2061148A Granted JPH02270998A (en) | 1990-03-14 | 1990-03-14 | Composite electroplated steel sheet having high corrosion resistance |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02270998A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2021055139A (en) * | 2019-09-30 | 2021-04-08 | 日本製鉄株式会社 | Production method of plating solution, plating solution, and production method of plated steel sheet using the same |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63103099A (en) * | 1986-10-17 | 1988-05-07 | Kao Corp | Organic polymer composite zinc and zinc alloy plated film and production thereof |
JPS63128198A (en) * | 1986-11-17 | 1988-05-31 | Kao Corp | Composite plated metallic material having superior adhesion to paint and corrosion resistance and its production |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
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JPS54146228A (en) * | 1978-05-08 | 1979-11-15 | Nippon Steel Corp | Zinc-plated steel sheet with superior corrosion resistance |
JPS5856039A (en) * | 1981-09-29 | 1983-04-02 | Fujitsu Ltd | Overlay control system for microprogram |
JPS60125395A (en) * | 1983-12-09 | 1985-07-04 | Kawasaki Steel Corp | Zn-alumina composite electroplated steel sheet having high corrosion resistance |
JPS60211095A (en) * | 1984-04-03 | 1985-10-23 | Kawasaki Steel Corp | Surface treated steel sheet having high corrosion resistance |
JPH0756080B2 (en) * | 1985-05-17 | 1995-06-14 | 花王株式会社 | Method for producing organic polymer composite metallurgical metal material with excellent paint adhesion |
JPS6314890A (en) * | 1986-07-05 | 1988-01-22 | Nippon Steel Corp | Decorative galvanized steel sheet and its production |
-
1990
- 1990-03-14 JP JP2061148A patent/JPH02270998A/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63103099A (en) * | 1986-10-17 | 1988-05-07 | Kao Corp | Organic polymer composite zinc and zinc alloy plated film and production thereof |
JPS63128198A (en) * | 1986-11-17 | 1988-05-31 | Kao Corp | Composite plated metallic material having superior adhesion to paint and corrosion resistance and its production |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2021055139A (en) * | 2019-09-30 | 2021-04-08 | 日本製鉄株式会社 | Production method of plating solution, plating solution, and production method of plated steel sheet using the same |
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