JP2004299979A - Surface preparation material for steel and method of surface- preparation - Google Patents
Surface preparation material for steel and method of surface- preparation Download PDFInfo
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- JP2004299979A JP2004299979A JP2003095853A JP2003095853A JP2004299979A JP 2004299979 A JP2004299979 A JP 2004299979A JP 2003095853 A JP2003095853 A JP 2003095853A JP 2003095853 A JP2003095853 A JP 2003095853A JP 2004299979 A JP2004299979 A JP 2004299979A
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Description
【0001】
【発明の属する技術分野】
本発明は、橋梁、タンク、橋脚、鉄骨、屋根等の鋼構造物を構成する鋼材表面に下地調整材として塗布される防錆効果の優れた下地調整材の技術分野に関するものである。
【0002】
【従来の技術】
従来から、橋梁等の鋼構造物は、長期間の使用を前提とするため、鋼の防食および外観確保を目的として表面が塗装されている。この場合に、塗装塗膜の耐久性が鋼構造物の期待耐用年数より短いため、複数回の塗り替え塗装が必要となる。一般環境用塗装系の塗膜劣化状態の調査結果では、新設塗装塗膜に比べて塗替え塗装塗膜の劣化進展は早いことが確認されている。これは、適用している塗装材に違いがない場合にも一般的に発生していることを考慮すれば、下地調整時残存したさび面上の塗膜が早期に劣化するためと考えられる。
これは、大気中で腐食した鋼は、例えば図1に示すように、鋼とさび層の界面近くに環境中の腐食を促進する因子(塩分等)である陰イオンが濃縮してネストとなる。ネストは、鋼の腐食で鋼表面に形成された腐食セルにより、陰イオンがアノード部に電気化学的に補足され濃縮したものであり、塗替え塗装塗膜下のネストが存在する部分では鋼材の腐食反応は抑制されない。このために、新設塗装塗膜にに比べて耐久性が劣ることになる。従って、塗装などの防食を施す場合に、さび層の除去のみならず、鋼とさび層界面に濃縮する腐食促進性の陰イオンの効果的な除去が必要となる。
ところで、塗替え塗装における腐食箇所の下地調整(素地調整)は、新設塗装時のように短期問で発生したさびの除去とは異なり、複数年をかけて生成したさび層の除去作業となる。このようなさび層およびネストの除去にはブラスト装置を用いる、あるいはディスクサンダーやエアーハンマー等の動力工具とハンマー、スクレーパーなどの手工具を併用して劣化個所を除去作業するなどの物理的な除去方法が一般に採用されている。しかし、鋼とさび層の界面に生成したネスト中の陰イオンは、前記のような物理的な除去作業では完全に除去できないといわれている。
そこで従来、塗替え塗装系の下地材として亜鉛等の防錆顔料を含有した塗料を塗布し、防錆する方法が実施されているが、このものは前記陰イオンを積極的に除去するものでないため、鋼表面でのさび発生の抑制効果に乏しく、塗替え塗装した場合、新規塗装の場合より短期間のうちにさびが発生するケースがある。そこで、下塗り材としてアルキルメタアクリレートの共重合体を含有する塗料を塗布し、これによって防錆効果を高めようとするものが提唱されている(特許文献1)。
【0003】
【特許文献1】
特開2000−42485号公報
【発明が解決しようとする課題】
ところが、前記特許文献1のものはさび発生の要因である陰イオンの外部からの侵入を阻止して防食性を向上しようとするものであって、ネスト中の陰イオンを除去するものでないため、仮に防錆効果に優れていたとしても塗替え塗装系の耐久性の改善が期待できるものではなく、ここに本発明の解決すべき課題がある。
【0004】
【課題を解決するための手段】
本発明は、このような実情に鑑み鋭意検討した結果、完成したものであって、請求項1の発明は、セメント系下地調整材に陰イオン吸着剤を含有することを特徴とする鋼材の下地調整材である。
請求項2の発明は、請求項1において、陰イオン吸着剤はセメントと反応して消費されることがないカルシウム・アルミニウム複合水酸化物であることを特徴とするものである。
請求項3の発明は、請求項1または2において、陰イオン吸着剤の含有量は、1.0重量%以上であることを特徴とするものである。
請求項4の発明は、陰イオン吸着剤を含有するセメント系下地調整材を鋼材に塗布するようにしたことを特徴とする鋼材の下地調整方法である。
そしてこれらのようにすることで、鋼材表面に付着する陰イオンの積極的な除去ができることになって、塗替え塗装の場合であっても鋼材の腐食を抑制し、塗装塗膜の耐久性が向上するとともに、鋼材自体の腐食からの保護も図れる。
【0005】
【発明の実施の形態】
本発明は、さび層と鋼材の界面に生成した陰イオンを積極的に除去して高い防錆効果を発揮し、もって塗替え周期の延伸等、塗替え塗装系の耐久性を向上させようとしたものである。下地調整材は、陰イオン吸着剤を添加したものであり、このような陰イオン吸着剤としては、セメントと反応して消費されることがないカルシウム・アルミニウム複合水酸化物、マグネシウム・アルミニウム複合水酸化物が適当で、具体的にはハイドロカルマイト、ハイドロタルサイトが例示されるが、ハイドロカルマイトは、特に鋼材腐食の促進因子として影響の大きい塩分の吸着能が高いものである。そして本発明が実施された下地調整材は、塗替え塗装時は勿論のこと、新規塗装をする場合に使用しても良いものである。
【0006】
本発明は、セメント系下地調整材を採用しているが、ここに採用されるセメントとしては、例えば普通ポルトランドセメント、アルミナセメント、早強セメント等、通常知られたセメントを採用することができる。
また、下地組成物としてはエポキシ樹脂が一般的であるが、アクリル樹脂等、通常知られた下地組成物を採用することができる。
さらにまた、下地調整材には、オクチルアルコール等の消泡材を添加したものでもよく、また塗装作業性の向上等のため炭酸カルシウム、カオリン等の充填材を添加したものであってもよい。
【0007】
陰イオン吸着剤の下地調整材への添加量は、好ましくは4.0重量%以上の範囲であり、さらに好ましくは8重量%以上である。陰イオン吸着剤の添加量が少ないと鋼材の表面にさび発生が発生してしまうことになり、また添加量が多くなると上塗り、中塗り等の塗装塗膜のふくれ抵抗性等を低下させる。
【0008】
以下、本発明を実験例によりさらに詳しく説明する。
【0009】
[供試体の作成]
供試体用の鋼板として、縦横100×100ミリメートル(mm)、厚さ1mmの冷間圧延鋼板(SS40)を用意し、この鋼板の表面を脱脂後、メッシュ#120のサンダーでケレンし、試験片を作成した。この試験片を、40℃の人工海水に48時間浸漬後、40℃の恒温槽内に50日間静置したが、この静置の間、24時間毎に人工海水を噴霧することでさびを発生させた。このさび発生の条件は、鋼材を海底トンネル内に1年間、曝露したと略同じものに相当することは既に他の実験により確認されている。そして該発生した鋼板のさびを肉眼では目視できない状態となるまでスクレーパーで除去した後、溶剤で汚れを除去し、その後、水洗し、乾燥させ、供試体を得た。
【0010】
[供試体の塗装実験]
前記得た供試体の表面について、図2に示す表図の条件で下地調整材を塗布し、3時間自然乾燥させた後、再度同じ下地調整材を塗布した。そして該塗布した供試体を、前記供試体にさびを発生させた場合に対し、静置期間が1月間であることを除いて同じ条件下でさび発生を試みた。尚、各実験において使用した供試体は3枚ずつとし、後述する結果についてはその平均とした。また、下地調整材は、水性エポキシ樹脂を混和材としたセメント系下地調整材で、セメントと炭酸カルシウムが1:1の重量比の割合で混入された水硬性粉体と、エポキシ樹脂およびポリアミドアミンを混和する混和材(反応性硬化剤)とを主成分としたもので、このようなものとして例えばアサヒボンド工業株式会社製の「レジアンダー」がある。また、陰イオン吸着剤としては塩分の吸着能が高いハイドロカルマイト(塩分吸着剤)を採用したが、このものとしては日本化学工業株式会社製の「ソルカット」がある。
【0011】
[結果と考察]
前記曝した供試体の表面を肉眼にて観察した結果を前記図2に示すとともに、塗布塗膜の補正自然電位を求めた。その結果を図3に示す。尚、補正自然電位の求め方は特許第3096240号に記載されるものである。ここで求められる補正自然電位から前記特許の手法と同じに鋼材の腐食度合いを知ることができることが確認されており、供試体に発生しているさびの促進度合いの指標となる。
【0012】
供試体表面の状態を肉眼で観察した結果、陰イオン吸着剤を入れないもの(試験番号1=ブランク)はひび割れが発生しているのが確認され、また塗膜を剥離したところ、供試体表面にさびの発生が確認された。一方、補正自然電位は−496ミリボルト(mV)であり、図4に示す補正自然電位と腐食度との関係から腐食度IVまたはVの範疇で、膨張性のさびが発生している状態である。塗膜を剥離したところ、供試体表面の全面にさびが発生しているのが確認された。
一方、塩分吸着剤を5/300(=1.67重量%)の重量比で入れたもの(試験番号2)は外観は良好であった。補正自然電位については−350mVで、腐食度としてはIIIの判定の範疇であった。塗膜を剥離したところ、供試体表面に点さびが生じていたが、前記試験番号1の場合に比してさび発生が明らかに抑制されていることが確認された。
さらに、塩分吸着剤を10/300(=3.33重量%)の重量比で入れたもの(試験番号3)の補正自然電位は−272mVで、腐食度としてはIIの範疇であり、供試体表面に僅かの点さびが発生しているのが塗膜の剥離後、目視により確認された。さび発生がこの程度であれば、実用上としては全く問題ないと判断される。
また、塩分吸着剤を30/300(=10.0重量%)の重量比で入れたもの(試験番号4)の補正自然電位は−209mVで、腐食度としてはさび発生のないIの範疇であり、また塗膜剥離後のさびの発生は目視では視認できず、さび発生は明らかに抑制されていることが確認された。
さらにまた、塩分吸着剤を50/300(=16.7重量%)の重量比で入れたもの(試験番号5)の補正自然電位は−204mVで、腐食度としてはさび発生のないIの範疇であり、また塗膜剥離後のさび発生は目視で視認できずさびの発生が抑制されていることが確認された。このものは試験番号4とほぼ同じ結果であることから、10.0重量%程度までが添加量として適当なものと判断される。
【0013】
【効果】
このように、本発明を実施したものにおいては、下地調整材に陰イオン吸着剤を含有させることで、さび層と鋼材の界面に生成するネスト中の陰イオンの積極的な除去ができることになって、塗替え塗装の場合であっても鋼材の腐食を抑制し、塗装塗膜の耐久性が向上するとともに、鋼材自体の腐食からの保護も図れることになる。
【図面の簡単な説明】
【図1】腐食セルの状態を示す概略図である。
【図2】試験条件およびその結果を目視したときの状態を示す表図である。
【図3】測定した自然電位を示すグラフ図である。
【図4】補正自然電位と腐食度との関係を示す表図である。[0001]
TECHNICAL FIELD OF THE INVENTION
TECHNICAL FIELD The present invention relates to a technical field of a base adjustment material excellent in rust prevention effect applied as a base adjustment material to a steel material surface constituting a steel structure such as a bridge, a tank, a pier, a steel frame, a roof, and the like.
[0002]
[Prior art]
BACKGROUND ART Conventionally, the surface of a steel structure such as a bridge has been painted for the purpose of preventing corrosion and ensuring the appearance of the steel, assuming long-term use. In this case, since the durability of the coating film is shorter than the expected service life of the steel structure, a plurality of repainting operations are required. Investigation results of the coating deterioration state of the coating system for general environment have confirmed that the deterioration progress of the repainted coating film is faster than that of the new coating film. This is considered to be due to the fact that the coating film on the rust surface remaining at the time of adjusting the base material deteriorates at an early stage, considering that the coating material generally occurs even when there is no difference in the applied coating material.
This is because, as shown in FIG. 1, for example, as shown in FIG. 1, anions, which are factors (salts and the like) that promote corrosion in the environment, are concentrated near the interface between the steel and the rust layer to form a nest. . The nest is a corrosion cell formed on the steel surface due to the corrosion of steel, and the anions are electrochemically captured and concentrated on the anode part. The corrosion reaction is not suppressed. For this reason, durability will be inferior compared with a newly-installed coating film. Therefore, when performing corrosion protection such as painting, it is necessary not only to remove the rust layer, but also to effectively remove corrosion-promoting anions that are concentrated at the interface between the steel and the rust layer.
By the way, the base adjustment (base adjustment) of the corroded part in the repainting is different from the removal of the rust generated in a short term as in the case of the new painting, and is a work of removing the rust layer generated over a plurality of years. Use a blasting device to remove such rust layers and nests, or physically remove such degraded parts using a power tool such as a disc sander or air hammer and a hand tool such as a hammer or scraper. The method is generally adopted. However, it is said that the anions in the nest formed at the interface between the steel and the rust layer cannot be completely removed by the physical removal operation as described above.
Therefore, conventionally, a method of applying a paint containing a rust-preventive pigment such as zinc as a base material of a repainting system has been carried out to prevent rust, but this method does not actively remove the anion. Therefore, the effect of suppressing the generation of rust on the steel surface is poor, and in the case of repainting, rust may occur in a shorter period of time than in the case of new coating. Therefore, a coating material containing a copolymer of an alkyl methacrylate is applied as an undercoating material to thereby enhance the rust prevention effect (Patent Document 1).
[0003]
[Patent Document 1]
Japanese Patent Application Laid-Open No. 2000-42485 [Problems to be Solved by the Invention]
However, the technique disclosed in
[0004]
[Means for Solving the Problems]
The present invention has been completed as a result of intensive studies in view of such circumstances, and the invention according to
According to a second aspect of the present invention, in the first aspect, the anion adsorbent is a calcium-aluminum composite hydroxide that is not consumed by reacting with the cement.
According to a third aspect of the present invention, in the first or second aspect, the content of the anion adsorbent is 1.0% by weight or more.
A fourth aspect of the present invention is a method for preparing a base material for a steel material, wherein a cement base material containing an anion adsorbent is applied to the steel material.
By doing so, it is possible to positively remove anions attached to the steel material surface, suppress corrosion of the steel material even in the case of repainting, and improve the durability of the paint film. As well as improving the protection of the steel itself from corrosion.
[0005]
BEST MODE FOR CARRYING OUT THE INVENTION
The present invention exerts a high rust-preventing effect by positively removing anions generated at the interface between the rust layer and the steel material, thereby improving the durability of the repainting system, such as stretching of the repainting cycle. It was done. The base adjusting material is a material to which an anion adsorbent is added. Examples of such an anion adsorbent include calcium-aluminum composite hydroxide and magnesium-aluminum composite water which are not consumed by reacting with cement. Oxides are suitable, and specific examples thereof include hydrocalmite and hydrotalcite. Hydrocalmite has a high ability to adsorb salts, which has a particularly great effect as a factor promoting corrosion of steel. The base adjustment material according to the present invention may be used not only at the time of repainting but also at the time of new coating.
[0006]
The present invention employs a cement-based base conditioner. As the cement employed here, for example, commonly known cements such as ordinary Portland cement, alumina cement, and early-strength cement can be employed.
As the base composition, an epoxy resin is generally used, but a commonly known base composition such as an acrylic resin can be used.
Furthermore, the base adjustment material may be a material to which an antifoaming material such as octyl alcohol is added, or a material to which a filler such as calcium carbonate, kaolin or the like is added to improve coating workability.
[0007]
The amount of the anion adsorbent added to the base material is preferably in the range of 4.0% by weight or more, more preferably 8% by weight or more. If the added amount of the anion adsorbent is small, rust is generated on the surface of the steel material, and if the added amount is large, the blistering resistance and the like of the paint film such as the top coat and the middle coat are reduced.
[0008]
Hereinafter, the present invention will be described in more detail with reference to experimental examples.
[0009]
[Preparation of specimen]
A cold-rolled steel plate (SS40) having a length of 100 mm and a width of 100 mm (mm) and a thickness of 1 mm was prepared as a steel plate for a specimen, the surface of the steel plate was degreased, and then quenched with a mesh # 120 sander. It was created. The test piece was immersed in artificial seawater at 40 ° C. for 48 hours, and then left standing in a thermostat at 40 ° C. for 50 days. During this standing, artificial seawater was sprayed every 24 hours to generate rust. I let it. It has already been confirmed by other experiments that the condition of the rust generation is substantially the same as the condition where the steel material was exposed to the undersea tunnel for one year. Then, the generated rust of the steel sheet was removed with a scraper until the rust became invisible to the naked eye, the stain was removed with a solvent, and then washed with water and dried to obtain a specimen.
[0010]
[Coating experiment of specimen]
The surface of the obtained specimen was coated with a base adjustment material under the conditions shown in the table in FIG. 2, allowed to dry naturally for 3 hours, and then coated with the same base adjustment material again. Then, with respect to the case where rust was generated on the test sample, rust generation was attempted under the same conditions except that the standing period was one month. The number of specimens used in each experiment was three, and the results described later were averaged. The base adjustment material is a cement-based base adjustment material containing an aqueous epoxy resin as an admixture, and a hydraulic powder in which cement and calcium carbonate are mixed at a weight ratio of 1: 1; And an admixture (reactive curing agent) that is a main component of the resin. Examples of such a material include "Register Under" manufactured by Asahi Bond Industrial Co., Ltd. As an anion adsorbent, hydrocalumite (salt adsorbent) having a high salt-adsorbing ability was used, and there is "Solcut" manufactured by Nippon Chemical Industry Co., Ltd.
[0011]
[Results and discussion]
The result of observing the surface of the exposed specimen with the naked eye is shown in FIG. 2, and the corrected natural potential of the applied coating film was obtained. The result is shown in FIG. The method of obtaining the corrected natural potential is described in Japanese Patent No. 3096240. It has been confirmed that the degree of corrosion of the steel material can be known from the corrected natural potential determined in the same manner as in the method of the patent, and this is an index of the degree of acceleration of rust generated in the test specimen.
[0012]
As a result of observing the state of the surface of the specimen with the naked eye, it was confirmed that cracks had occurred in the specimen without an anion adsorbent (
On the other hand, the one containing the salt adsorbent at a weight ratio of 5/300 (= 1.67% by weight) (Test No. 2) had a good appearance. The corrected spontaneous potential was -350 mV, and the corrosion degree was in the category of judgment of III. When the coating film was peeled off, spot rust was formed on the surface of the test piece, but it was confirmed that rust generation was clearly suppressed as compared with the case of Test No. 1.
Furthermore, the corrected natural potential of the sample containing the salt adsorbent in a weight ratio of 10/300 (= 3.33% by weight) (test number 3) was -272 mV, and the corrosion degree was in the category of II. After the peeling of the coating film, it was visually confirmed that slight rust was generated on the surface. If the occurrence of rust is at this level, it is judged that there is no problem in practical use.
The corrected natural potential of the sample containing the salt adsorbent in a weight ratio of 30/300 (= 10.0% by weight) (test number 4) was -209 mV, and the corrosion degree was in the category of I without rust. In addition, the occurrence of rust after the coating film was peeled was not visually observed, and it was confirmed that the occurrence of rust was clearly suppressed.
Furthermore, the corrected natural potential of a sample containing a salt adsorbent in a weight ratio of 50/300 (= 16.7% by weight) (test number 5) was -204 mV, and the corrosion degree was in the range of I without rusting. Further, it was confirmed that rusting after peeling of the coating film was not visually observed, and the occurrence of rust was suppressed. Since the result was almost the same as that of Test No. 4, it was judged that up to about 10.0% by weight was appropriate as an addition amount.
[0013]
【effect】
As described above, in the embodiment of the present invention, by including the anion adsorbent in the base adjustment material, the anion in the nest generated at the interface between the rust layer and the steel material can be positively removed. Therefore, even in the case of repainting, corrosion of the steel material is suppressed, the durability of the coating film is improved, and the steel material itself can be protected from corrosion.
[Brief description of the drawings]
FIG. 1 is a schematic diagram showing a state of a corrosion cell.
FIG. 2 is a table showing test conditions and a state when the results are visually observed.
FIG. 3 is a graph showing a measured self potential.
FIG. 4 is a table showing the relationship between the corrected natural potential and the degree of corrosion.
Claims (4)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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JP2003095853A JP4343570B2 (en) | 2003-03-31 | 2003-03-31 | Steel base material and base material adjustment method |
Applications Claiming Priority (1)
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
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KR101049630B1 (en) * | 2006-04-18 | 2011-07-14 | 다이니폰 도료 가부시키가이샤 | High durability repair painting method |
JP2017193768A (en) * | 2016-04-22 | 2017-10-26 | ショーボンド建設株式会社 | Surface treatment method for steel materials, and surface treatment agent |
JP2018059104A (en) * | 2017-10-18 | 2018-04-12 | 株式会社ジェイアール総研エンジニアリング | Anticorrosive undercoat material for steel material |
CN111574895A (en) * | 2019-02-18 | 2020-08-25 | 蓝伟荣 | Metal rusty anticorrosive primer |
US20210197334A1 (en) * | 2019-12-25 | 2021-07-01 | Fanuc Corporation | Drive mechanism for transfer tool |
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
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KR101049630B1 (en) * | 2006-04-18 | 2011-07-14 | 다이니폰 도료 가부시키가이샤 | High durability repair painting method |
JP2017193768A (en) * | 2016-04-22 | 2017-10-26 | ショーボンド建設株式会社 | Surface treatment method for steel materials, and surface treatment agent |
JP2018059104A (en) * | 2017-10-18 | 2018-04-12 | 株式会社ジェイアール総研エンジニアリング | Anticorrosive undercoat material for steel material |
CN111574895A (en) * | 2019-02-18 | 2020-08-25 | 蓝伟荣 | Metal rusty anticorrosive primer |
US20210197334A1 (en) * | 2019-12-25 | 2021-07-01 | Fanuc Corporation | Drive mechanism for transfer tool |
US11850694B2 (en) * | 2019-12-25 | 2023-12-26 | Fanuc Corporation | Drive mechanism for transfer tool |
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