JPS5950182A - Removing method of al melt-sprayed film - Google Patents

Removing method of al melt-sprayed film

Info

Publication number
JPS5950182A
JPS5950182A JP16060082A JP16060082A JPS5950182A JP S5950182 A JPS5950182 A JP S5950182A JP 16060082 A JP16060082 A JP 16060082A JP 16060082 A JP16060082 A JP 16060082A JP S5950182 A JPS5950182 A JP S5950182A
Authority
JP
Japan
Prior art keywords
melt
coated
coating
range
viscosity
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.)
Pending
Application number
JP16060082A
Other languages
Japanese (ja)
Inventor
Kazuhiko Oda
一彦 織田
Hiroyuki Suzuki
博幸 鈴木
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.)
Nippon Steel Corp
Original Assignee
Sumitomo Metal Industries 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 Sumitomo Metal Industries Ltd filed Critical Sumitomo Metal Industries Ltd
Priority to JP16060082A priority Critical patent/JPS5950182A/en
Publication of JPS5950182A publication Critical patent/JPS5950182A/en
Pending 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
    • C23FNON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F1/00Etching metallic material by chemical means
    • C23F1/10Etching compositions
    • C23F1/14Aqueous compositions
    • C23F1/32Alkaline compositions
    • C23F1/36Alkaline compositions for etching aluminium or alloys thereof
    • 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
    • C23FNON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
    • C23F1/00Etching metallic material by chemical means
    • C23F1/44Compositions for etching metallic material from a metallic material substrate of different composition

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • ing And Chemical Polishing (AREA)

Abstract

PURPOSE:To improve efficiency and safety and to enable the removal of an Al melt-sprayed film at a low cost by performing said removal by a chemical treatment in place of mechanical grinding. CONSTITUTION:An aq. NaOH soln. is coated on an Al melt-sprayed steel plate and is brought into reaction with Al to form sodium aluminate in the case of removing only the Al melt sprayed film in the specified range near the weld line of said steel plate. The Al melt-sprayed film which is hardly strippable is converted to the above-described Al compd. which is easily strippable, then said compd. can be removed by, for example, washing. However, the aq. NaOH soln. when coated in this case spreads to the outside of the specified range. Thereupon, the aq. NaOH soln. incorporated with 0.5-3.0wt% alpha-starch to have viscosity is coated thereon. Such aq. soln. flows after coating and the coated range expands slightly but the flowing range is uniform and can be predicted and limited with respect to a specified coated amt., because the liquid surface dries to hardness and the liquid is internally agitated by foaming, by which the reaction with the Al is effectively accelerated.

Description

【発明の詳細な説明】 この発明はA2溶剤皮膜を能率よくかつ低コストで除去
し得るAAiWAt溶射皮膜方法に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an AAiWAt thermal spray coating method that can remove A2 solvent coatings efficiently and at low cost.

鋼板VCズ1するAt溶剤メッキは防食性にすぐれてい
るためタンク等の大型銅板建造物の防食に多く用いられ
ている。
At solvent plating on steel plates has excellent anti-corrosion properties and is therefore often used for anti-corrosion of large copper plate structures such as tanks.

タンク等のAt溶射による防食は従来、組立て完了後の
タンク等に対して作業員の手でAt溶射をイーYう現場
m月、I’1iJi Iの方法で行われていだが、最近
、IiQ鉄工場内で品質にすぐれたAt溶射鋼板の能率
的な製造がイ1われるようになり、このA2溶川1i1
板を用いる方法がむE来よりコヌト、品質、生産性にす
ぐれるだめ、タンク等の防食1段として普及しつつある
Corrosion protection by At spraying on tanks, etc. has traditionally been carried out on-site by workers manually spraying At on tanks, etc. after assembly has been completed, but recently, IiQ Ironworks has Efficient production of high-quality At sprayed steel sheets in-house has become possible, and this A2 Yukawa 1i1
Since the method of using plates has been superior in quality and productivity, it has become popular as a first step in corrosion protection for tanks, etc.

上記A7溶剤鋼板は建設現場で主として浴1便によりタ
ンク等に組立てられるが、At溶射皮膜を残したま捷で
溶接すると溶接欠陥を生じ易いため、溶接施工前に予め
溶接線イ」近のAt溶射皮膜を除去しておかなければな
らない。またタンク等の使用開始時の定められた検査で
行われる磁粉探傷では、At溶射皮膜の上からの欠陥検
出能がAt溶射皮膜の無い場合((比較して劣るだめ、
磁粉探傷を行う個所のAt溶射皮膜は予め除去しておく
必要がある。
The above-mentioned A7 solvent steel sheets are mainly assembled into tanks, etc. at construction sites using a single bath. However, since welding with a welding method that leaves the At thermal spray coating remains, welding defects are likely to occur. The film must be removed. In addition, in magnetic particle flaw detection, which is carried out in a prescribed inspection at the beginning of use of tanks, etc., the ability to detect defects from above the At sprayed coating is poor when there is no At sprayed coating ((in comparison, it is inferior).
It is necessary to remove the At sprayed coating in advance at the locations where magnetic particle testing is to be performed.

コノヨうなA7溶則皮)Iψの除去には従来、クライン
ダーによる研削の手法が採られていだが、このクライン
ダーイυ[削には次のような欠点があった。
Conventionally, grinding with a grinder has been used to remove the A7 molten skin) Iψ, but this grinding with a grinder has the following drawbacks.

■ クラインダーの砥粒を細かぐすると目詰シを生じ作
柴の継続が不可能となる。寸だ前記砥tl′fを粗くす
るとAt溶牙]皮膜下の鋼板素地にまで研削が及A7で
研削面が粗くなる。このだめ適正な研削条件の範囲が擾
めて狭く、能率面、コヌ+−+47で問題がある。
■ If the grinder's abrasive grains are too fine, it will cause clogging, making it impossible to continue using the grinder. When the grinding wheel tl'f is made coarser, the grinding reaches to the base steel plate under the At molten coating, and the ground surface becomes rough at A7. As a result, the range of appropriate grinding conditions is narrowed and there is a problem in terms of efficiency.

■ 0(削による粉塵の発生が著るしく、作業環境が劣
化し、安全衛生面で問題がある・ 本発明は上記問題を解消すべくなてれたものであって、
除去しようとする特定範囲のA7溶剤皮11’Aを剥離
し易い化合物に変える化学的処理を施してから除去する
ことにより、能率、安全性にすぐれ、かつ低コストでの
除去を可能とするAt溶射皮11免の除去方法の提供を
目的とする。
■ 0 (Dust generated by scraping is significant, the working environment deteriorates, and there are health and safety problems.) The present invention was developed to solve the above problems, and
By performing a chemical treatment to convert the A7 solvent skin 11'A in a specific range to be removed into a compound that is easy to peel off, At can be removed with high efficiency, safety, and low cost. The purpose of this invention is to provide a method for removing thermal spray skin.

本発明者らは、上記特定範囲のAt溶射皮膜の除去方法
の開発についてy+@・研究を重ねだ結果、グラインダ
ーの如@観械的研削によるA7溶射皮膜の除去処]月1
に代えて、薬液処理によりA、/=熔射皮膜を剥メ1(
シ易い化合物に変えた後例えば水洗除去するという化学
的処理の方法で除去処理することによって、能率、安全
性にすぐれ、かつ、低コストでのA7溶躬皮膜除去が可
能になるという事実が明ら〃1となった。
As a result of repeated research on the development of a method for removing the At thermal spray coating in the above-mentioned specific range, the inventors of the present invention have found that the method for removing the A7 thermal spray coating by visual grinding using a grinder is as follows:
Instead, the chemical treatment was used to remove A, / = sprayed coating 1 (
It is clear that by changing the compound to a compound that is easy to remove and then chemically removing it by washing with water, it is possible to remove the A7 melting film with high efficiency and safety, and at a low cost. Ra〃 became 1.

すなわち、AJ−浴η、1皮膜はA5粒子が鋼板素地と
密に結合して生T&妊れた皮11であるから、基本的に
(r!、 At皮膜にアルカリ、例えばNaOH4の水
溶液を塗布しNaOHとAlとを反応σせてアルミン酸
す) ’) ラム(、NaAt、0.24 nH120
) f生成式せ、剥1ift l−;J Eel;’z
A/溶躬皮溶金皮膜%i[L易い10記アルミ化合物に
変えることけ容易に考えられるところである。
That is, since the AJ-bath η, 1 film is a raw T & pregnant skin 11 in which A5 particles are tightly bonded to the steel sheet substrate, basically (r!, an aqueous solution of an alkali, such as NaOH4, is applied to the At film. NaOH and Al are reacted to form aluminic acid)') Lamb (, NaAt, 0.24 nH120
) f generation formula, strip 1ift l-;J Eel;'z
A/It is easily possible to change the molten metal coating %i [L to a 10 aluminum compound.

しかし、上記の溶接線付近の如き特定範囲のAl溶射皮
膜のみを除去しようとする場合、前記範囲内のA7皮膜
の全膜厚に亘ってAtと反応してアルミン酸ナトリウム
を生成させるに十分な量のNa・OH水溶液を塗布する
と、このNaOH水溶液に上記特定範囲の外に捷で拡が
り、余分のAt溶射皮膜まで除去して品質ケ損う不都合
を生じる。そこで仮りに上記NaOH水溶液の拡がりを
何等かの方法で阻止して上記特定範囲内に留めることが
可能であれば、上記不都合は排除し得ると考えられる。
However, when attempting to remove only the Al sprayed coating in a specific area such as near the weld line mentioned above, the entire thickness of the A7 coating within the above range is sufficient to react with At and produce sodium aluminate. When a large amount of the Na.OH aqueous solution is applied, the NaOH aqueous solution spreads outside the above-mentioned specific range, and even the excess At sprayed coating is removed, resulting in a problem of quality deterioration. Therefore, if it were possible to prevent the spread of the NaOH aqueous solution by some method and keep it within the specified range, the above-mentioned disadvantages could be eliminated.

なお上記NaOH水溶液の拡がりを阻止する方法として
は、上記特定範囲の外周に」是を1114築する物理的
な拡がシ阻止の方法と溶液自体に粘性を1′力だせる化
学的な阻止方法とが考えらizる。i’+i1者の物理
的方法は経済的に附加であるので後者の化学的方法につ
いてさらに検討を重ねた。その結果、N0101[水溶
液に粘結剤を添加して適正な粘性を付与することによっ
てnIJ記溶液の流動範囲が規正でれ、」二記特定範囲
夕)−・の溶液の拡が9の阻止が笑月1上可能であると
いう事実が判明した。
As methods for preventing the NaOH aqueous solution from spreading, there are two methods: a physical method of preventing the spread by building a barrier around the periphery of the specific range, and a chemical method of preventing the spread by applying viscosity to the solution itself. I can't help but think about it. Since the physical method of i'+i1 is economically additional, the latter chemical method was further investigated. As a result, the flow range of the solution in N0101 [nIJ can be regulated by adding a binder to the aqueous solution to give it an appropriate viscosity, and the spread of the solution in the specified range (2) is prevented in 9. It turns out that this is possible on the first day of the month.

すなわち、例えば適当濃度のNaOH水溶液に適正量の
α醍粉を含有はせた溶液は、NaOHの化学的活性を損
うこと無しに適度な粘性を保持することが7)J能であ
る。前記溶液をAt溶射皮膜に塗布すると、塗布後、溶
液は流動して塗布範囲は若干拡大するが、その流動範囲
が均一で、一定の塗布罪に対しその流動1161囲を予
測して限定することが火月」上可能であるので、流動範
囲を規制することが一+iJ能となる。これ(は液の表
面部が乾いて固くなる/こめで、その内部においては、
液がNa0I−IとAAとの反応による発泡で攪拌きれ
るため、液全体のmη、j皮1tlNj中のA4との反
応が効果的に促進でれ、短11.lj間にアルミン酸す
tllラム生成が促進される。
That is, for example, a solution containing an appropriate amount of α-powder in a NaOH aqueous solution of an appropriate concentration has the ability to maintain an appropriate viscosity without impairing the chemical activity of NaOH. When the above solution is applied to the At thermal spray coating, the solution flows after application and the application range expands slightly, but the flow range is uniform and the flow 1161 area should be predicted and limited for a certain amount of coating. Since it is possible on "Tuesday", regulating the flow range becomes 1+iJ ability. This is a temple where the surface of the liquid dries and becomes hard; inside it,
Since the liquid is completely stirred by foaming due to the reaction between Na0I-I and AA, the reaction with A4 in the entire liquid mη,j skin 1tlNj is effectively promoted, and short 11. During lj, aluminic acid tllram production is promoted.

このように、Af惰躬皮膜中のALヲ変えて生成したア
ルミン酸ナトリウムは、tiiljめて剥1iif L
易い性質を有するので高圧水による水洗もしくけタワシ
等の軟研磨で容易に除去し得るので、従来のクラインダ
ーの如き強力な43+、q械的研削は不要となり上記能
率低下安全衛生上の問題も解消し1!+る。
In this way, the sodium aluminate produced by changing the AL in the Af inertia film can be removed by peeling off.
Because of its easy-to-clean properties, it can be easily removed by washing with high-pressure water or by soft polishing with a scourer, eliminating the need for the powerful 43+, q mechanical grinding of conventional grinders, and eliminating the above-mentioned efficiency reduction and safety and health problems. Resolved 1! +ru.

本発明は上記知見に基いてなされたものでろって、その
要旨とするところは、α鉱粉を重お比で0.5〜3.0
%含有てせ粘性を持たせたアルカリ水溶液をAt溶射皮
膜に塗布し、Atを剥ht++シ易いアルミン酸塩に変
えて除去することを特徴とするAt浴射皮I!桑の除去
方法にある。
The present invention has been made based on the above knowledge, and its gist is that α ore powder has a weight ratio of 0.5 to 3.0.
At bath spray coating I! which is characterized by applying an aqueous alkaline solution containing 0.9% viscosity to the At thermal spray coating and converting the At into an aluminate that is easy to remove. It is in the method of removing mulberry.

本発明方法において、At溶躬皮11ψ中のAtと反応
8せて剥祷し易いアルミン酸塩を生成させるアルカリ水
溶液としては、苛性ソーダ(NaOH)の水溶液が代表
的なものであるが、この他アンモニア(NH3) 、水
酸化力/L/ シウム(ca(OH,)2)、水酸化カ
リウム(KOH)の水溶液等でも同様の剥に1し易いア
ルミン酸塩が得られる。
In the method of the present invention, an aqueous solution of caustic soda (NaOH) is typical as the alkaline aqueous solution that reacts with At in the At fused skin 11ψ to produce an aluminate that is easy to peel off. Similar aluminates that are easy to peel can also be obtained using aqueous solutions of ammonia (NH3), hydration power/L/sium (ca(OH,)2), potassium hydroxide (KOH), and the like.

上記アルカリ水溶液の濃度としては、アルカリの種類に
より活性に大小があって一律には規定できないが、例え
ばNaOHの場合は含有量が25%以上の7農度の水溶
合りとすることが好ましい。
The concentration of the aqueous alkali solution cannot be uniformly defined because the activity varies depending on the type of alkali, but for example, in the case of NaOH, it is preferable to set the concentration to 7 degrees of water solubility with a content of 25% or more.

〃′に本発明方法においてアルカリ水1・省i夜に粘性
を持たせる薬剤としてα1・殴粉を用い、その含有量を
上記の々II<限定した理由、につ・ハて説明する。
In the method of the present invention, α1 and flour are used as agents for imparting viscosity to alkaline water, and the reason why the content thereof is limited to the above-mentioned values will be explained below.

α叙イ分にアルカリ水溶液に添加した場合、アルカリの
11う性、例えばAlとアルカリ水溶液との反応性およ
びf’+iJ記反応の際に生じる活溌な発泡攪拌Wを損
うことなしにアルカリ水溶液に適度の粘性をもたせるこ
とが可能であるので、粘性イτ1与剤として最適である
When added to an alkaline aqueous solution in the amount of α, the alkaline aqueous solution can be added without impairing the 11 opacity of the alkali, for example, the reactivity of Al with the alkali aqueous solution, and the active foaming stirring W that occurs during the f'+iJ reaction. Since it is possible to give a suitable viscosity to the material, it is most suitable as a viscosity τ1 imparting agent.

αIiυ粉の含有量を05〜3.0%(重量%)に限定
したのは、05%未満では粘性が過少で、塗布後のアル
カリ水溶液の流動を所定範囲内に限定する目的に71 
して不十分である。また30%を越えると粘性が過大と
なって、塗布後Atとアルカリとの反応が十分に進行し
ない間に塗布液が固化してl、 4うのでアルミン酸塩
の生成が不十分となシAl溶η・1皮11Qjの良好な
剥PillI生’;< ?−!!ることが困つ(1[と
なるからである。
The reason why the content of αIiυ powder was limited to 0.5% to 3.0% (wt%) was because if it was less than 0.5%, the viscosity was too low, and the purpose was to limit the flow of the alkaline aqueous solution after application to within a predetermined range.
It is insufficient. Moreover, if it exceeds 30%, the viscosity becomes excessive and the coating solution solidifies before the reaction between At and the alkali progresses sufficiently after coating, resulting in insufficient aluminate formation. Good peeling of Al-molten η・1 skin 11Qj';<? -! ! It is difficult to do so (1[).

なお、α赦粉の他に、粘が1:の向」二作用があり、か
つアルカリ水溶液とA4との反応による発泡IW拌の障
害にならない、例えば鉄粉、合金11ifl粉等の含有
は差し支えない。
In addition to the α-permeable powder, it is permissible to include iron powder, alloy 11ifl powder, etc., which have a dual action with a viscosity of 1: and do not interfere with foaming IW stirring due to the reaction between the alkaline aqueous solution and A4. do not have.

次に本発明の効果を実施IMI VCより説明する。Next, the effects of the present invention will be explained by implementing IMI VC.

実施例1 鋼板上にtj+j(厚250μに溶射したA7浴射皮1
i5j全水平に置き、その上から、濃度を秤々に変えた
NaOH水溶液にα赦粉を不発明範叩内で添加量を種々
に変えて含有せしめた塗布液を、倹膜781〜2絹、塗
布範囲3 Q m=s fの円形に塗布して本発明例の
供試材とした。寸だ比較のだめ、上記と同様のAl溶射
皮j1φ上に、同様のNaOH水溶液水溶液α本粉明範
囲から外れた;頭囲で2市々に変えて含有せしめだ塗布
液を、同様の塗膜厚、塗布範囲に塗布して比較例の供試
材とした。
Example 1 A7 bath coating 1 sprayed on a steel plate to a thickness of 250μ
i5j was placed completely horizontally, and from above, a coating solution containing α-powder in various amounts within the non-inventive range was added to a NaOH aqueous solution of varying concentrations. , a circular coating area of 3 Q m = s f was applied to provide a sample material of the present invention example. For comparison purposes, a similar coating solution containing a similar NaOH aqueous solution α (which is outside the range of this powder) was applied to the same Al thermal sprayed coating J1φ as above; A sample material of a comparative example was prepared by coating the coating thickness and coating range.

上記2例の各供試料を、塗布後24時間放tiTの後塗
布面を水洗しながらタワシで改か〈几・擦する方法で反
応生成物を除去して、その剥ぬ1の状態による反応生成
物の剥1’iii姓の良否のt・F filliと、1
1]記127布後の々了布液の流動の拡がり及び均一性
ならびに今市j1か中での液とA2との反応による発泡
攪拌の4人混の観乞′シ結果による塗布液粘性の過不足
の評価とによって供試料のAt溶溶度皮膜除去の成績を
判定した。
After applying TiT for 24 hours after application, each test sample in the above two examples was washed with water and scrubbed with a scrubbing brush to remove the reaction products. Peeling of the product 1'iii t・F filli of the quality of the surname, 1
1] The spread and uniformity of the flow of the liquid after the 127th application, and the viscosity of the coating liquid based on the results of a four-person observation of the foaming and stirring caused by the reaction between the liquid and A2 in Imaichi J1. The performance of removing the At-soluble film of the test sample was determined based on the evaluation of excess and deficiency.

]S4結果を捷とめて第1表に示す。] The S4 results are summarized and shown in Table 1.

第   1   表 表中、剥1.vift性評価((カ1の○印は塗布した
範囲について面積率で50%以上埼厭([シたもので、
剥1jiii性良、△印は10〜50%の範囲で刺ト4
1[シたもので、fl!I々不良、X印は剥離が10%
未満のもので、不良を示す。まだ粘性評価側の○印(φ
塗布復液に若干流動するが、その範囲が均一で、かつ目
標塗布範囲(30龍$)を少し越えてlQ**以内にと
どまったもので、粘性が適正なもの、Δ印は塗布抜液は
殆んど流動せず、反応が十分に進行しないまま固化した
もので、粘性が過大なもの、X印は塗布抜液の流動範囲
が目標範囲をlO■以上に大[11に越えて拡がったも
ので、粘性の過少なものを示す。
In Table 1, peeling 1. Vift property evaluation
Peeling is 1jiii good, △ mark is 4 in the range of 10 to 50%.
1 [Shitamono, fl! I defects, X mark indicates 10% peeling.
Anything less than that indicates a defect. The ○ mark (φ) is still on the viscosity evaluation side.
There is some flow in the coating liquid, but the range is uniform and it stays within lQ** slightly beyond the target coating range (30 dragon dollars), and the viscosity is appropriate. There is almost no fluidity, and the reaction has solidified before it has progressed sufficiently, and the viscosity is excessive. This indicates that the viscosity is too low.

表に見る通シ、比較例■は剥;:11″1イ1ミは良好
であるが、粘性が過少で塗布液が目オW4範囲を大1’
] K越えて拡がり不良であった。比較例■U−■と同
様粘性が過少で不良であった。比較例■(1粘性が過大
で塗布後の液の流動が少ガく、反応が十分に進行しない
まま固化し剥j、l:iL性が硝々不良であった。比較
例■(−1:粘性が極めて過大で塗布抜液は殆んど流動
せず、反応か進行しない寸ま1:す1化し、剥離性が不
良であった。これに対し本発明例■〜■げいずれものb
磁粉の含有11tが適当であり適正な粘性であつ/hの
で、ケ布腋の拡がりも均一で適切な範囲にとどオシ、反
応も十分に進行して良好な剥離性が得られて特定範囲の
A2溶剖皮膜の除去VC列して良好な成績を示しだ。
As shown in the table, Comparative Example ■ peels off;
] It spread beyond K and was defective. Similar to Comparative Example ``U-■'', the viscosity was too low and was poor. Comparative Example ■(1) The viscosity was too high, and the liquid flowed poorly after application, and the reaction solidified and peeled off without proceeding sufficiently. Comparative Example ■(-1 : The viscosity was extremely excessive, and the applied liquid hardly flowed, and the reaction did not proceed.
Since the magnetic powder content of 11 tons is appropriate and the viscosity is appropriate/h, the spread of the underarm is uniform and within the appropriate range, and the reaction progresses sufficiently to obtain good peelability and can be applied within a specific range. The A2 lytic membrane removal VC column showed good results.

以上の説明から明らかな如く、本発明のAll溶度皮膜
除去方法に、従来のグラインダー研削による直接除去に
代えて、特定範囲のA7溶射皮膜に化学的処理を施して
剥帰し易い化合物に変えてからl’ii’i単な水洗等
によシ除去するものであり、除去の能率、安全性の向上
及びコストの低減が図れるので、At溶射鋼板を用いる
建造物の防食コストの低減、4」8没作柴の能率の向上
に顕著な効果を発揮するものである。
As is clear from the above explanation, the method for removing the All-soluble coating of the present invention involves chemically treating a specific range of the A7 thermal spray coating to convert it into a compound that easily peels off, instead of the conventional direct removal by grinding. It can be removed by simple washing with water, etc., which improves removal efficiency, safety, and reduces costs, reducing corrosion protection costs for buildings using At thermal sprayed steel sheets. It has a remarkable effect on improving the efficiency of 8-year-old plants.

出願人  住友金属工業株式会社 代理人弁理士  生 形 元 重、、、、、H,、、:
、5凶 自発手続補正書 昭和57年10月υ「1 特許庁長官 若杉和火  殿 1、事件の表示 昭和57年特許願第160600号 2 発明の名称 A7溶射皮膜の除去方法 3 補正をする者 事件との関係 特許出願人 住 所   大阪市東区北浜5丁目15番地名 称 (
211)住友金属工業株式会社代表者  nμ 谷 典
 文 4代理人 6 補正の対象 明イ、in 7jAの「発明の詳細な説明」の欄7、 
補正の内容 (1)明、■書のMy 2頁第7行から同第1211に
かけて「まだタンク等の使用開始時の定められた・・・
・・A4溶坏1皮膜は予め除去しておく必要がある。」
とあるのを[またタンク等の検査で行われる磁粉探傷で
は、At熔射皮膜の上からの欠陥検出能がAt溶剤皮1
1ψの無い場合に比較して劣るだめ、At膜厚と必要検
査出能との関係によってに磁粉探傷を行う個所のAt浴
射皮膜を予め除去する場合がある。」に補正し寸す。
Applicant Sumitomo Metal Industries Co., Ltd. Representative Patent Attorney: Shigemoto H.:
, 5 Voluntary procedure amendment dated October 1982 1. Commissioner of the Japan Patent Office Kazuhiro Wakasugi 1. Indication of the case 1989 Patent Application No. 160600 2. Title of the invention A7. Method for removing thermal spray coating 3. Person making the amendment Relationship to the incident Patent applicant address 5-15 Kitahama, Higashi-ku, Osaka Name (
211) Sumitomo Metal Industries Co., Ltd. Representative nμ Norihiro Tani 4 Agent 6 Subject of amendment Mei, in 7jA column 7 of “Detailed description of the invention”
Contents of the amendment (1) From page 2 of My, line 7 to line 1211 of Book ■, ``It is still the case that the stipulated conditions at the time of the start of use of tanks, etc.''
...The A4 melting layer 1 film must be removed in advance. ”
[Also, in magnetic particle flaw detection performed in inspections of tanks, etc., the ability to detect defects from above the At spray coating is as low as At solvent coating 1.
Depending on the relationship between the At film thickness and the required inspection output, the At bath spray coating may be removed in advance at the location where magnetic particle testing is to be performed, since it is inferior to the case without 1ψ. ”.

Claims (1)

【特許請求の範囲】[Claims] (1)α磁粉を重量比で0.5〜3.0%含有芒せ粘性
を持たせたアルカリ水溶液をAA熔射皮膜に塗布し、A
tを剥聞1し易いアルミン酸塩に変えて除去することを
特徴とするAt溶射皮膜の除去方法。
(1) Apply an alkaline aqueous solution containing 0.5 to 3.0% by weight of α magnetic powder and give it viscosity to the AA spray coating.
A method for removing an At thermal spray coating, characterized in that T is removed by changing it to an aluminate that is susceptible to peeling.
JP16060082A 1982-09-13 1982-09-13 Removing method of al melt-sprayed film Pending JPS5950182A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16060082A JPS5950182A (en) 1982-09-13 1982-09-13 Removing method of al melt-sprayed film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP16060082A JPS5950182A (en) 1982-09-13 1982-09-13 Removing method of al melt-sprayed film

Publications (1)

Publication Number Publication Date
JPS5950182A true JPS5950182A (en) 1984-03-23

Family

ID=15718442

Family Applications (1)

Application Number Title Priority Date Filing Date
JP16060082A Pending JPS5950182A (en) 1982-09-13 1982-09-13 Removing method of al melt-sprayed film

Country Status (1)

Country Link
JP (1) JPS5950182A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108842153A (en) * 2018-05-16 2018-11-20 深圳仕上电子科技有限公司 Utilize the method for potassium hydroxide solution removing aluminium film

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108842153A (en) * 2018-05-16 2018-11-20 深圳仕上电子科技有限公司 Utilize the method for potassium hydroxide solution removing aluminium film

Similar Documents

Publication Publication Date Title
Bo et al. Effect of Mg and RE on the surface properties of hot dipped Zn–23Al–0.3 Si coatings
JPH057147B2 (en)
CN112410791B (en) High-speed environment-friendly chemical stripping solution for nickel coating and preparation method thereof
JPH0125831B2 (en)
CN106967968B (en) High-efficiency environment friendly steel derusting conjunctiva agent and preparation method thereof
JPS59211576A (en) Method for removing sprayed al or zn film
US4270932A (en) Polishing of silver-plated articles
JPS5950182A (en) Removing method of al melt-sprayed film
JPS62260083A (en) Method for chemically cleaning surface of stainless steel
US6481449B1 (en) Ultrasonic metal finishing
TW412600B (en) Surface treatment process for hot-dip zinciferous plated steel sheet
CN106011812B (en) The preparation method of aluminum alloy surface silanization conversion film
JPS62260082A (en) Method for chemically cleaning surface of stainless steel
JPS62260081A (en) Method for chemically cleaning surface of stainless steel
CN111118516A (en) Preparation method of efficient rust remover for outdoor building steel and stone
US4509992A (en) Processes and compositions for the treatment of aluminum surfaces
JPS6320494A (en) Method for chemically cleaning surface of stainless steel
Dennis et al. Brush plating
US2951768A (en) Chemical removal of zinc coating from iron
JPH05106059A (en) Continuous zinc coating treatment for aluminum strip
JPS6092483A (en) Production of galvanized steel sheet
CN115341202B (en) Activating solution for aluminum alloy before chemical nickel plating and pretreatment method
US3658565A (en) Parting compound containing chromium oxide manganese dioxide and a liquid inorganic carrier
WO2018223440A1 (en) Metal derusting and anti-rust sealing agent and preparation method thereof
JP2696652B2 (en) Rust prevention method for glass-lined reaction tank