Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JPH0230748B2 - - Google Patents
[go: Go Back, main page]

JPH0230748B2 - - Google Patents

Info

Publication number
JPH0230748B2
JPH0230748B2 JP61144012A JP14401286A JPH0230748B2 JP H0230748 B2 JPH0230748 B2 JP H0230748B2 JP 61144012 A JP61144012 A JP 61144012A JP 14401286 A JP14401286 A JP 14401286A JP H0230748 B2 JPH0230748 B2 JP H0230748B2
Authority
JP
Japan
Prior art keywords
iron
underwater
metal
rust
metals
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP61144012A
Other languages
Japanese (ja)
Other versions
JPS631488A (en
Inventor
Minoru Kitayama
Hiroshi Masuda
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.)
Chugoku Marine Paints Ltd
Original Assignee
Chugoku Marine Paints Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Chugoku Marine Paints Ltd filed Critical Chugoku Marine Paints Ltd
Priority to JP14401286A priority Critical patent/JPS631488A/en
Publication of JPS631488A publication Critical patent/JPS631488A/en
Publication of JPH0230748B2 publication Critical patent/JPH0230748B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Application Of Or Painting With Fluid Materials (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

(産業上の利用分野) 本発明は、鉄鋼構造物に水中硬化塗料を塗布す
るための前処理方法に関するものである。 (従来の技術) 従来から水中(湿潤面や海中を含む)での塗装
用塗料は、エポキシ系、ウレタン系などの樹脂に
硬化機能はもとより海中ヌレ性に影響がある塗料
中に巻き込まれた水分の影響緩和や不活性化を図
るためにアミン基等を有する硬化剤を使用してい
る。 (発明が解決しようとする課題) しかしその反面、このような硬化剤を使用する
と塗膜形成後の塗膜の一次密着性に影響を及ぼす
などの副作用があつて、自ずから添加量に限度が
ある。 また海上、海中鉄鋼構造物補修工事における海
水中での塗付前処理は、陸上での作業と同様錆面
を水中サンドブラストによつてSIS Sa2.5以上、
または錆面をパワーブラシでST−3まで研磨し
て素地調整を行うか、場合によつてはブラスト後
更にパワーブラシ調整を行うなどするが、この時
露出される鉄面は、活性面であり、急速に酸化を
受け易く、極めて赤錆の発生し易い環境にある。
そのため活性面に直ちに赤錆が発生し、この赤錆
は海水中であるため、含水酸化鉄でそれ自体コロ
イド状であるばかりでなく、海中のアミノ基を有
する無機的、有機的並びに生物学的浮遊物と反応
してコロイド状となり鉄被塗物面を覆い海中ヌレ
性を著しく阻害する。 このように3%食塩人工海水では容易にヌレ可
能なアミノ基を含む水中硬化塗料といえどアミノ
基をもつ無機的、有機的並びに浮遊生物体の量に
よつて著しく影響を受ける。 この対策として、被塗付面から発生する鉄イオ
ンと容易に錯塩を形成し、鉄イオンを不活性化す
る物質を樹脂または硬化剤に添加する方法が考え
られるが、これらの添加は塗膜の他の特性例えば
一次密着性に影響があつて自ずから添加に制限が
ある。 そこで本発明の目的は、塗膜性能に影響しない
鉄鋼構造物への海中ヌレ性の良い塗装前処理方法
を提供することにある。 (課題を解決するための手段) 本発明の特徴は、水中での鉄鋼構造物に水中硬
化塗料を塗布補修する際、サンドブラストまたは
研磨材などを用いる手作業による錆落し時(同時
またはその直後に含む)に、この錆落し作業に生
じた粗面溝を利用して鉄より電気化学的に卑な金
属またはそれらの合金をブラツシ内に装着し、こ
のブラツシによつて、上記粗面溝に上記金属を付
着させることである。 また本発明の他の特徴は、水中での鉄鋼構造物
に水中硬化塗料を塗布補修する際のブラストによ
る錆落し作業の最終段階に、鉄より電気化学的に
卑な金属またはそれらの合金からなる箔を鉄活性
面に当てがい、ブラストを利用して、錆落し粗面
に上記金属を付着させることにある。 本発明にいう鉄より電気化学的に卑な金属もし
くは合金とは、マグネシウム、亜鉛、アルミニウ
ム及びそれらの二種あるいはそれ以上の金属種の
合金をいうが、これらの中にもちろん一般的に単
一金属としては酸化し易くて得難い鉄より卑な金
属、カリウム、カルシウム、ナトリウム等や鉄よ
り電気化学的に貴であつても材料として取り扱い
易い材質を確保するために添加し、合金として鉄
より卑であればよく、これら添加金属別主成分が
合金中に含まれることは当然である。例えば鉄、
ニツケル、錫、鉛、銅などである。 ここで本発明が開発するに至る経緯を説明す
る。 いわゆる水中硬化塗料を用いて種々の海域にお
ける海中ヌレ性を検討した結果、無機的、有機的
並びに生物学的アミノ基を有する浮遊物を持つ海
水中といえど、被塗装物が亜鉛、アルミニウム、
金属硅素では良好な海中ヌレ性を示すものであつ
て、前記のような海水中におけるヌレ性に著しく
影響を与える現象は、鉄またはその構造物の特異
な現象であることがわかつた。すなわち初期腐食
による溶出鉄水和イオンが大きくヌレ性阻害に関
わつていることを見出した。従つてステンレスス
チールの場合は、その不錆性から海中ヌレ性に及
ぼす影響の度合が鉄に比べてかなり少ないことが
考えられ、また実験的にも立証し得た。 この事から海中ヌレ性劣化現象を防止する対策
としての有力な手段の一つとしては、海中鉄鋼構
造物を水中硬化塗料によつて塗付補修する場合、
水中サンドブラスト、パワーブラシにて錆落しを
するが、この時に直ちに活性化された面から水中
塗装されるまでの間に溶出される鉄水和イオンを
防止するか不活性化すればよいのである。 そこで前記したように亜鉛、アルミニウム等の
面では海中ヌレ性の影響のないことから、鉄より
電気化学的に卑な金属もしくは合金を生じた鉄活
性面に付着させることにより、それらの金属また
は合金が恰も犠牲陽極となつて活性鉄面からの鉄
水和イオンの溶出を防ぐことにならないかと考え
た。すなわち鉄活性面の生成と同時に犠牲極金属
を簡単に付着させることである。 一般的に水中塗装は、その硬化時間と作業性の
面からほぼ一時間程度であり、鉄面からの鉄水和
イオンの溶出防止は、その時間内で鉄より卑な金
属または合金による鉄水和イオン溶出を防止さえ
すればよいのである。 そこで本発明の内容を詳細に説明すると、海中
鉄鋼構造物を水中サンドブラストにて錆落しをし
た後、水中塗装前にパワーブラシによる手作業錆
落しをするが、その際の最終段階で鉄より電気化
学的に卑な金属もしくは合金をパワーブラシ内に
装着させたものを用いるものであつて、ブラスト
活性面に摺動し、鉄粗面にそれら鉄より卑な金属
もしくは合金を付着させるものである。なお鉄よ
り電気化学的に卑な金属は、一般的に鉄より柔か
く、これら金属を内着装させたパワーブラシでは
これら金属もしくは合金からなる棒のみが消費さ
れる。従つてこの金属を補充する必要のあること
はいうまでもない。 また水中サンドブラストによる被塗付鉄鋼構造
物の錆落しをするその最終段階で、金属または合
金の箔を鉄活性面に当てがつたのち、水中サンド
ブラストを打つと、この金属または合金の箔が部
分的に鉄活性面に転写される。これらの付着金属
または合金からなる箔が活性鉄面からの鉄水和イ
オンの溶出を防ぎ、塗付性のよい作業を行うこと
ができるものである。この金属または合金箔の活
性面への当て方としては、磁石を用いれば簡単に
できる。この方法は金属もしくは合金付着量が作
業時間によつて鉄からの鉄水和イオン溶出防止に
不足と考える場合に極めて有効である。 通常約1時間内に鉄の発錆を防止する為の鉄よ
り電気化学的に卑な金属例えば亜鉛の海水浸漬に
よる消費量は約0.12g/m2hrであり(塩水噴霧の
場合約1.0g/m2hr)、一方海中でブラスト粗面に
手作業による亜鉛など先述金属の摺動によつて付
着する量は実験の結果約15g/m2まで可能である
ことがわかつた。なお一般的に電気めつき法によ
る目付量3g/m2であれば亜鉛被覆率は約100%
となるが、本方法の場合は様子が異なる。 また本摺動法によつて得難い付着量15g/m2
上必要な場合には、前述のようにサンドブラスト
法によつて亜鉛転写し所定の付着量を得ることが
できる。この時の付着量は当てがう亜鉛箔厚みと
シヨツト処理時間によつて自由に選択し得る。 鉄の水和酸化物の溶出を活性面に於いて1時間
防ぐためには金属種によつて多少異なるが、少な
くとも1g/m2〜5g/m2が必要であり、必ずし
もこれら金属によつて表面を100%覆う必要はな
い。 海中塗装作業時間内に海中での鉄の発錆を防止
する鉄より電気化学的に卑な金属の最小量を鉄の
表面に確保することが必要なのである。 (発明の効果) 本発明は、以上の構成を有するので、水中であ
る環境からこれら付着金属腐食生成物の大部分は
水中に洗われ、また残るとしても水和酸化物であ
り、これは塗膜の一次密着性に殆ど影響しない。 (実施例) 本発明の実施例を別紙に説明する。
(Industrial Application Field) The present invention relates to a pretreatment method for applying an underwater curing paint to a steel structure. (Prior art) Paints for painting underwater (including on wet surfaces and under the sea) have traditionally had a hardening function due to resins such as epoxy and urethane, but water entrapped in the paint has an effect on underwater wettability. Curing agents containing amine groups, etc. are used to alleviate the effects of and deactivate. (Problem to be solved by the invention) However, on the other hand, when such a curing agent is used, there are side effects such as affecting the primary adhesion of the coating after coating film formation, and there is a natural limit to the amount added. . In addition, pre-painting treatment in seawater for repair work on offshore and underwater steel structures involves sandblasting the rusted surface under water, similar to work done on land, to achieve a SIS Sa of 2.5 or higher.
Alternatively, the rusted surface may be polished to ST-3 with a power brush to prepare the surface, or in some cases, further power brush adjustment may be performed after blasting, but the iron surface exposed at this time is an active surface. It is in an environment that is susceptible to rapid oxidation and is extremely susceptible to red rust.
As a result, red rust immediately forms on the active surface, and since this red rust is in seawater, it is not only hydrated iron oxide and colloidal in itself, but also contains inorganic, organic, and biological floating substances with amino groups in the sea. It reacts with the metal and forms a colloid, covering the surface of the steel object and significantly inhibiting its underwater wetting properties. As described above, in 3% saline artificial seawater, even underwater curing paints containing amino groups that can be easily wetted are significantly affected by the amount of inorganic, organic, and suspended organisms that have amino groups. As a countermeasure to this problem, it is possible to add a substance to the resin or curing agent that easily forms a complex salt with the iron ions generated from the surface to be coated and inactivates the iron ions, but these additions may damage the coating film. Since it affects other properties such as primary adhesion, there are limits to its addition. SUMMARY OF THE INVENTION Therefore, an object of the present invention is to provide a coating pretreatment method that does not affect coating performance and has good underwater wetting properties on steel structures. (Means for Solving the Problems) A feature of the present invention is that when repairing submersible steel structures by applying an underwater curing paint, during manual rust removal using sandblasting or abrasives (at the same time or immediately after) ), a metal that is electrochemically more base than iron or an alloy thereof is installed in the brush using the rough grooves created during this rust removal work, and the brush is used to fill the rough grooves with metals that are electrochemically more base than iron. It is the attachment of metal. Another feature of the present invention is that metals that are electrochemically less noble than iron or alloys thereof are used in the final stage of rust removal work by blasting when applying and repairing underwater curing paint to steel structures underwater. The purpose is to apply the foil to the active iron surface and use blasting to adhere the metal to the rust-removed rough surface. The metals or alloys that are electrochemically more base than iron as used in the present invention include magnesium, zinc, aluminum, and alloys of two or more of these metals. It is added to ensure a metal that is easier to handle as a material, such as potassium, calcium, sodium, etc., which is easier to oxidize and is difficult to obtain as a metal, and a material that is easier to handle as a material even though it is electrochemically nobler than iron. It is only necessary that the main components of these additive metals are included in the alloy. For example, iron
These include nickel, tin, lead, and copper. Here, the circumstances leading to the development of the present invention will be explained. As a result of examining underwater wettability in various sea areas using so-called underwater curing paints, we found that even though the seawater contains suspended matter containing inorganic, organic, and biological amino groups, the coating material is zinc, aluminum,
Metallic silicon exhibits good wettability in seawater, and it has been found that the phenomenon that significantly affects the wettability in seawater as described above is a unique phenomenon of iron or its structures. In other words, it was found that hydrated iron ions eluted due to initial corrosion are largely involved in inhibiting wetting properties. Therefore, in the case of stainless steel, it is thought that the degree of influence on underwater wettability due to its rust resistance is considerably smaller than that of iron, and this has also been experimentally proven. Therefore, one of the effective measures to prevent the deterioration of underwater wetness is when repairing underwater steel structures by applying underwater curing paint.
Rust is removed using underwater sandblasting and power brushing, but at this time it is necessary to prevent or inactivate the iron hydrate ions that are eluted from the activated surface immediately before being painted underwater. Therefore, as mentioned above, surfaces such as zinc and aluminum are not affected by underwater wettability, so by attaching metals or alloys that are electrochemically less base than iron to the activated iron surface, it is possible to remove these metals or alloys. It was thought that this would act as a sacrificial anode and prevent the elution of iron hydrated ions from the active iron surface. That is, the sacrificial electrode metal can be simply attached at the same time as the iron active surface is generated. In general, underwater painting takes approximately one hour in terms of curing time and workability, and it is possible to prevent the elution of iron hydrated ions from iron surfaces within that time by applying iron water using metals or alloys baser than iron. All that is required is to prevent the elution of ions. Therefore, to explain the content of the present invention in detail, after removing rust from underwater steel structures by underwater sandblasting, manual rust removal using a power brush is performed before underwater painting. This uses a power brush with chemically base metals or alloys installed inside the power brush, which slides on the blast active surface and causes the metals or alloys baser than iron to adhere to the rough iron surface. . Note that metals that are electrochemically less noble than iron are generally softer than iron, and in a power brush equipped with these metals, only rods made of these metals or alloys are consumed. Therefore, it goes without saying that this metal needs to be replenished. In addition, in the final stage of removing rust from a steel structure by underwater sandblasting, if a metal or alloy foil is applied to the active surface of the iron and then underwater sandblasting is applied, the metal or alloy foil may be partially removed. is transferred to the iron-active surface. The foil made of these deposited metals or alloys prevents the elution of hydrated iron ions from the active iron surface, allowing work to be performed with good applicability. This metal or alloy foil can be easily applied to the active surface by using a magnet. This method is extremely effective when it is considered that the amount of metal or alloy deposited is insufficient to prevent the elution of iron hydrated ions from the iron over time. Normally, the amount consumed by immersing a metal electrochemically less noble than iron, such as zinc, in seawater to prevent rusting in about 1 hour is about 0.12 g/m 2 hr (about 1.0 g in the case of salt spray). On the other hand, as a result of experiments, it was found that the amount of the metals mentioned above, such as zinc, deposited on rough blasted surfaces by manual sliding in the sea can be up to about 15 g/m 2 . Generally, if the area weight is 3g/ m2 by electroplating method, the zinc coverage will be approximately 100%.
However, in the case of this method, the situation is different. In addition, if a coating weight of 15 g/m 2 or more is required, which is difficult to obtain by the present sliding method, the predetermined coating weight can be obtained by transferring zinc by the sandblasting method as described above. The amount of coating at this time can be freely selected depending on the thickness of the zinc foil and the shot processing time. In order to prevent the elution of hydrated iron oxides on the active surface for one hour, at least 1 g/m 2 to 5 g/m 2 is required, although it varies somewhat depending on the metal type. It is not necessary to cover 100%. It is necessary to secure a minimum amount of a metal that is electrochemically more base than iron on the surface of the iron to prevent rusting of the iron under the sea during the time of the underwater painting operation. (Effects of the Invention) Since the present invention has the above configuration, most of these deposited metal corrosion products are washed away in water from a certain environment, and even if they remain, they are hydrated oxides, which are not coated. It has almost no effect on the primary adhesion of the film. (Example) An example of the present invention will be described in a separate sheet.

【表】【table】

【表】【table】

【表】【table】

Claims (1)

【特許請求の範囲】 1 水中での鉄鋼構造物に水中硬化塗料を塗布補
修する際の錆落し時に、この錆落し作業に生じた
粗面溝を利用して鉄より電気化学的に卑な金属ま
たはそれらの合金をブラツシ内に装着し、このブ
ラツシによつて上記粗面溝に上記金属を付着させ
ることを特徴とする鉄鋼構造物の塗装前処理方
法。 2 水中での鉄鋼構造物に水中硬化塗料を塗布補
修する際のブラストによる錆落し作業の最終段階
に、鉄より電気化学的に卑な金属またはそれらの
合金からなる箔を鉄活性面に当てがい、ブラスト
を利用して、錆落し粗面に上記金属を付着させる
ことを特徴とする鉄鋼構造物の塗装前処理方法。
[Scope of Claims] 1. When removing rust when repairing underwater curing paint on steel structures under water, the rough surface grooves created during the rust removal work are used to remove metals that are electrochemically more base than iron. Alternatively, a method for pre-painting a steel structure, characterized in that an alloy thereof is installed in a brush, and the brush adheres the metal to the rough surface grooves. 2. In the final stage of rust removal work by blasting when applying and repairing underwater curing paint to steel structures underwater, a foil made of a metal that is electrochemically less noble than iron or an alloy thereof is applied to the active surface of the iron. , a method for pre-painting a steel structure, characterized in that the metal is adhered to a rough rust-removed surface using blasting.
JP14401286A 1986-06-21 1986-06-21 Painting pretreatment of steel structure Granted JPS631488A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14401286A JPS631488A (en) 1986-06-21 1986-06-21 Painting pretreatment of steel structure

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14401286A JPS631488A (en) 1986-06-21 1986-06-21 Painting pretreatment of steel structure

Publications (2)

Publication Number Publication Date
JPS631488A JPS631488A (en) 1988-01-06
JPH0230748B2 true JPH0230748B2 (en) 1990-07-09

Family

ID=15352265

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14401286A Granted JPS631488A (en) 1986-06-21 1986-06-21 Painting pretreatment of steel structure

Country Status (1)

Country Link
JP (1) JPS631488A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6209645B2 (en) * 2016-01-08 2017-10-04 株式会社横河ブリッジ Steel repainting method

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0613108B2 (en) * 1986-01-21 1994-02-23 新日本製鐵株式会社 Underwater coating base treatment method

Also Published As

Publication number Publication date
JPS631488A (en) 1988-01-06

Similar Documents

Publication Publication Date Title
ATE518922T1 (en) METHOD FOR THE PRETREATMENT OR/AND COATING OF METAL SURFACES PRIOR TO FORMING WITH A PAINT-LIKE COATING AND USE OF THE SUCH COATED SUBSTRATES
DE69201707D1 (en) Chromium-free process and composition for the protection of aluminum.
JP6609725B2 (en) Reactive paint for steel that provides high corrosion resistance
WO2014020665A1 (en) Coating and coated steel
FI69094C (en) FOERFARANDE FOER RENING AV ROSTSKYDDANDE AV EN METALLYTA
US3598659A (en) Method for producing a corrosion-resistant coating upon metals and corrosion-resistant coatings so-produced
US4098928A (en) Method of coating underwater metal surfaces
NO834813L (en) ANTI-FILLING COATS FOR A SURFACE OF A VESSEL OR MARINE CONSTRUCTION.
JPH0230748B2 (en)
WO2021206048A1 (en) Coating material and coated steel material
US5575865A (en) Process for coating a workpiece of steel with an anti-corrosive agent
JPH10204654A (en) Metal surface treatment method
JPS58219274A (en) Corrosion resistant cathode anticorrosion paint
JPH0613108B2 (en) Underwater coating base treatment method
JP2007056327A (en) Arc type metal thermal spraying method
JPS63265627A (en) Surface coated steel material and its manufacture
EP1003923A1 (en) Metal spraying
JPH09206675A (en) Method for preventing rust in rusting face
JPS59100084A (en) Contamination resisting method for outer board of ship hull
JPH06248473A (en) Corrosion preventing method for hot-dip aluminized steel
JPS60251972A (en) Method for inhibiting corrosion of sharp edge part of steel structure
JPH0625361B2 (en) Blast material
JPH03180497A (en) Surface treatment of steel
JPH10506831A (en) Surface treated, corrosion protected metal objects and methods of treating objects to prevent corrosion
JPS62146282A (en) Method for preventing contamination of propeller for ship