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JPH0422213B2 - - Google Patents
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JPH0422213B2 - - Google Patents

Info

Publication number
JPH0422213B2
JPH0422213B2 JP17945584A JP17945584A JPH0422213B2 JP H0422213 B2 JPH0422213 B2 JP H0422213B2 JP 17945584 A JP17945584 A JP 17945584A JP 17945584 A JP17945584 A JP 17945584A JP H0422213 B2 JPH0422213 B2 JP H0422213B2
Authority
JP
Japan
Prior art keywords
present
weight
surfactant
carbonate
detection agent
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
Application number
JP17945584A
Other languages
Japanese (ja)
Other versions
JPS6157829A (en
Inventor
Tsutomu Matsushita
Hikari Matsuo
Munetaka Tsuro
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.)
Mitsubishi Heavy Industries Ltd
Original Assignee
Mitsubishi Heavy 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 Mitsubishi Heavy Industries Ltd filed Critical Mitsubishi Heavy Industries Ltd
Priority to JP17945584A priority Critical patent/JPS6157829A/en
Publication of JPS6157829A publication Critical patent/JPS6157829A/en
Publication of JPH0422213B2 publication Critical patent/JPH0422213B2/ja
Granted legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01MTESTING STATIC OR DYNAMIC BALANCE OF MACHINES OR STRUCTURES; TESTING OF STRUCTURES OR APPARATUS, NOT OTHERWISE PROVIDED FOR
    • G01M3/00Investigating fluid-tightness of structures
    • G01M3/02Investigating fluid-tightness of structures by using fluid or vacuum
    • G01M3/04Investigating fluid-tightness of structures by using fluid or vacuum by detecting the presence of fluid at the leakage point
    • G01M3/12Investigating fluid-tightness of structures by using fluid or vacuum by detecting the presence of fluid at the leakage point by observing elastic covers or coatings, e.g. soapy water

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Examining Or Testing Airtightness (AREA)
  • Preventing Corrosion Or Incrustation Of Metals (AREA)

Description

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

〔本発明の産業分野〕 本発明は、船体、各種タンク、圧力容器、配管
などの気密又は水密を必要とする構造物内に圧縮
空気などを送入し、構造物表面に起泡液を塗布し
てその発泡の有無によつて気体の漏洩を検知する
ための気体漏洩検査用検知剤、すなわち、気圧試
験用漏洩検出剤に関する。 〔従来技術〕 従来この分野には、石鹸あるいは合成洗剤、多
くは、アルキルベンゼンスルホン酸塩、脂肪酸エ
タノールアミド、アルキルフエノールポリオキシ
エチレンエーテル、高級アルコールポリオキシエ
チレンエーテル等の各種界面活性剤を起泡剤と
し、被検体の腐食防止のために亜硝酸塩、リン酸
塩、ホウ酸塩、安息香酸塩、セバシン酸塩等を適
量添加したものが使用されている。 〔上記従来技術の欠点〕 しかし、これらの検知剤を使用した場合、検知
作業後含有している界面活性剤、高分子剤、無機
塩類が水分の蒸発によつて粘着状に、あるいは、
白く析出する状態で残留する。気圧試験を行つた
機器類の外面は塗装されることが通常であるが、
これら残留物を除去することなく直接塗装を行う
と、金属面に対する塗料の密着性が著しく阻害さ
れ、剥離、変色等を惹起するに至り、美観を損う
ばかりでなく品質管理上大きな問題となる。 従つて、検知剤の残留物を除去することになる
が、対象が大型である程新たな問題が生じる。す
なわち、船舶、タンク等において流水、あるいは
噴射水のもとでブラツシングしながら除去する
が、水洗途中から既に発錆するので除去後、サー
ンダ、ワイヤブラシ等での除錆作業も必要とな
る。これらに要する経費、工期はコスト低減を阻
害する一つになつている。 〔本発明の目的〕 本発明は、従来の漏洩検知剤を塗布した場合に
生ずる残留物を除去するため、作業を省略して経
費節減、工期短縮を行い、かつ、発錆事故を排除
しうる気圧試験用漏洩検知剤を提供することを目
的とする。すなわち、本発明は、検知作業後に、
残留物の除去作業を要せず、そのまま塗装しても
塗膜の密着性を阻害しない気圧試験用漏洩検知剤
を提供することを目的とする。 〔本発明の構成〕 そして、本発明は、上記目的を達成するため
に、低濃度の界面活性剤を起泡剤として、また、
炭酸のアンモニウム塩を防食剤として配合するも
のである。すなわち、本発明は、炭酸のアンモニ
ウム塩0.05〜2重量%、界面活性剤0.01〜0.05重
量%の混合水溶液からなることを特徴とする気圧
試験用漏洩検知剤である。 泡の発生、安定性を得るためには、界面活性剤
の中から起泡力のあるものを任意に設定すること
も可能であるが、特に低濃度で性能を発揮するも
のが良好であることは当然である。したがつて、
本発明で使用できる界面活性剤としては、起泡性
の良好なものであれば任意のものでも良いが、特
に好ましいものとして、ノニルフエノールポリエ
チレンエーテル(エチレンオキサイド10〜20モル
付加)、ラウリルアルコールポリオキシエチレン
エーテル(エチレンオキサイド8〜16モル付加)
が起泡性、安定性とも優れている。 これらの界面活性剤は0.01〜0.05重量%の範囲
で使用できる。0.05重量%を超えると塗料の密着
性に影響し、0.01重量%未満では起泡性、安定性
が欠如するので検知能力が低下するので好ましく
ない。 一方、本発明において、防食剤として添加する
炭酸のアンモニウム塩は、溶液で鉄表面に塗布さ
れると、これに不働態化皮膜を形成し、しかも完
全に気化、揮発して残査を止どめることがないと
いう性状を有する。この炭酸のアンモニウム塩と
しては、炭酸アンモニウム、炭酸水素アンモニウ
ム又は、炭酸アンモニウム、炭酸水素アンモニウ
ム間の任意の中和度の炭酸塩が使用できる。使用
濃度は0.05〜2重量%の範囲で使用できる。2重
量%を超えての使用は過剰防錆となるので不必要
である。又、揮散してしまうのに時間を要し、検
知後短時間のうちに塗装する場合ふさわしくな
い。また0.05重量%未満では防錆力が不足するの
で好ましくない。 本発明では、起泡力の優良な界面活性剤の低濃
度を使用し、これに炭酸のアンモニウムを添加す
ることによつて、検知する鉄鋼表面に塗布して水
分が蒸発しても残留物を止どめることがなく、し
かも、良好な防錆能も有するものであり、その結
果、従来除去のために行つていた水洗、ブラツシ
ング等が不要となり、直ちに塗装作業を行うこと
ができるものである。 以下、本発明の具体例を発明品としてあげ、従
来の検知剤2種(従来品A、B)との比較を行つ
た。検知剤の種類、試験項目及びその結果を次の
表に示す。
[Industrial field of the present invention] The present invention is a method for applying compressed air or the like into structures that require airtightness or watertightness, such as ship hulls, various tanks, pressure vessels, and piping, and applying a foaming liquid to the surface of the structure. The present invention relates to a gas leakage detection agent for detecting gas leakage based on the presence or absence of foaming, that is, a leakage detection agent for atmospheric pressure testing. [Prior art] Conventionally, in this field, soaps or synthetic detergents, often using various surfactants such as alkylbenzene sulfonates, fatty acid ethanolamides, alkylphenol polyoxyethylene ethers, and higher alcohol polyoxyethylene ethers, are used as foaming agents. In order to prevent corrosion of the specimen, a suitable amount of nitrite, phosphate, borate, benzoate, sebacate, etc. is added. [Disadvantages of the above conventional techniques] However, when these detection agents are used, the surfactants, polymer agents, and inorganic salts contained in them become sticky or sticky due to evaporation of water after the detection operation.
It remains as a white precipitate. The exterior surfaces of equipment subjected to barometric pressure tests are usually painted;
If paint is applied directly without removing these residues, the adhesion of the paint to the metal surface will be significantly impaired, leading to peeling, discoloration, etc., which not only impairs the aesthetics but also poses a major quality control problem. . Therefore, the residue of the detection agent must be removed, but new problems arise as the object becomes larger. That is, it is removed by brushing under running water or jet water in ships, tanks, etc., but since rust has already formed during washing with water, it is necessary to use a saunder, wire brush, etc. to remove rust after removal. The expenses and construction period required for these are one of the obstacles to cost reduction. [Object of the present invention] The present invention eliminates the residue that occurs when applying a conventional leak detection agent, thereby saving costs and shortening the construction period by omitting the work, and eliminating rusting accidents. The purpose is to provide a leak detection agent for atmospheric pressure tests. That is, in the present invention, after the detection work,
To provide a leak detection agent for atmospheric pressure tests that does not require work to remove residues and does not impede the adhesion of the paint film even if it is applied as is. [Structure of the present invention] In order to achieve the above object, the present invention uses a surfactant at a low concentration as a foaming agent, and
It is formulated with ammonium carbonate salt as an anticorrosion agent. That is, the present invention is a leak detection agent for atmospheric pressure tests characterized by comprising a mixed aqueous solution of 0.05 to 2% by weight of an ammonium salt of carbonate and 0.01 to 0.05% by weight of a surfactant. In order to generate foam and obtain stability, it is possible to select any surfactant that has foaming power, but it is especially desirable to use a surfactant that exhibits good performance at low concentrations. Of course. Therefore,
The surfactant that can be used in the present invention may be any surfactant as long as it has good foaming properties, but particularly preferred ones include nonylphenol polyethylene ether (addition of 10 to 20 moles of ethylene oxide), lauryl alcohol polyethylene ether, Oxyethylene ether (8 to 16 moles of ethylene oxide added)
It has excellent foaming properties and stability. These surfactants can be used in amounts ranging from 0.01 to 0.05% by weight. If it exceeds 0.05% by weight, it will affect the adhesion of the paint, and if it is less than 0.01% by weight, it will lack foaming properties and stability, which will lower the detection ability, which is not preferable. On the other hand, in the present invention, when the ammonium salt of carbonate added as a corrosion inhibitor is applied as a solution to the iron surface, it forms a passivation film on the iron surface and completely vaporizes and volatilizes, leaving no residue. It has the property that it never gets wet. As the ammonium salt of carbonic acid, ammonium carbonate, ammonium hydrogen carbonate, or a carbonate having any degree of neutralization between ammonium carbonate and ammonium hydrogen carbonate can be used. The concentration used can range from 0.05 to 2% by weight. Use of more than 2% by weight is unnecessary as it will result in excessive rust prevention. In addition, it takes time for it to volatilize, making it unsuitable for painting within a short period of time after detection. Further, if it is less than 0.05% by weight, the rust preventive power will be insufficient, which is not preferable. In the present invention, by using a low concentration of a surfactant with excellent foaming power and adding ammonium carbonate to this, it is applied to the steel surface to be detected and no residue remains even when the water evaporates. It does not rust and has good rust prevention properties, and as a result, it eliminates the need for washing with water, brushing, etc., which were conventionally used for removal, and can be painted immediately. It is. Hereinafter, specific examples of the present invention will be cited as invention products, and comparisons will be made with two conventional detection agents (conventional products A and B). The type of detection agent, test items, and results are shown in the table below.

【表】【table】

〔本発明の効果〕[Effects of the present invention]

本発明は、以上詳記したように、従来技術に比
較して、残留物となる物質が極端に小さく、その
結果、検査後これを除去することなく塗装しても
塗膜に少しの障害を与えない顕著な効果が生ずる
ものである。
As detailed above, in the present invention, the amount of residual substances is extremely small compared to the conventional technology, and as a result, even if the residue is painted without being removed after inspection, there is no problem with the paint film. It produces a remarkable effect that does not give any effect.

Claims (1)

【特許請求の範囲】[Claims] 1 炭酸のアンモニウム塩0.05〜2重量%、界面
活性剤0.01〜0.05重量%の混合水溶液からなるこ
とを特徴とする気圧試験用漏洩検知剤。
1. A leak detection agent for atmospheric pressure tests, comprising an aqueous mixed solution of 0.05 to 2% by weight of an ammonium salt of carbonate and 0.01 to 0.05% by weight of a surfactant.
JP17945584A 1984-08-30 1984-08-30 Leakage detecting agent for barometric test Granted JPS6157829A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17945584A JPS6157829A (en) 1984-08-30 1984-08-30 Leakage detecting agent for barometric test

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17945584A JPS6157829A (en) 1984-08-30 1984-08-30 Leakage detecting agent for barometric test

Publications (2)

Publication Number Publication Date
JPS6157829A JPS6157829A (en) 1986-03-24
JPH0422213B2 true JPH0422213B2 (en) 1992-04-16

Family

ID=16066152

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17945584A Granted JPS6157829A (en) 1984-08-30 1984-08-30 Leakage detecting agent for barometric test

Country Status (1)

Country Link
JP (1) JPS6157829A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009063406A (en) * 2007-09-06 2009-03-26 Yokogawa Electric Corp Irradiation condensing device
CN113092028B (en) * 2021-04-07 2021-11-02 广东润和新材料科技有限公司 Aircraft oxygen system leak detection agent and preparation method thereof

Also Published As

Publication number Publication date
JPS6157829A (en) 1986-03-24

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