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
Links
- 238000001514 detection method Methods 0.000 claims description 15
- 239000003795 chemical substances by application Substances 0.000 claims description 13
- 239000004094 surface-active agent Substances 0.000 claims description 11
- 238000012360 testing method Methods 0.000 claims description 7
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 4
- 150000003863 ammonium salts Chemical class 0.000 claims description 4
- 239000011259 mixed solution Substances 0.000 claims 1
- 238000005187 foaming Methods 0.000 description 7
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 5
- 239000001099 ammonium carbonate Substances 0.000 description 5
- 239000003973 paint Substances 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- -1 alkylbenzene sulfonates Chemical class 0.000 description 3
- 235000012501 ammonium carbonate Nutrition 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 2
- 230000001680 brushing effect Effects 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 239000004088 foaming agent Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920000056 polyoxyethylene ether Polymers 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- BVTJGGGYKAMDBN-UHFFFAOYSA-N Dioxetane Chemical compound C1COO1 BVTJGGGYKAMDBN-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- PRKQVKDSMLBJBJ-UHFFFAOYSA-N ammonium carbonate Chemical compound N.N.OC(O)=O PRKQVKDSMLBJBJ-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 238000002161 passivation Methods 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 238000003908 quality control method Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229940116351 sebacate Drugs 0.000 description 1
- CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000271 synthetic detergent Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01M—TESTING STATIC OR DYNAMIC BALANCE OF MACHINES OR STRUCTURES; TESTING OF STRUCTURES OR APPARATUS, NOT OTHERWISE PROVIDED FOR
- G01M3/00—Investigating fluid-tightness of structures
- G01M3/02—Investigating fluid-tightness of structures by using fluid or vacuum
- G01M3/04—Investigating fluid-tightness of structures by using fluid or vacuum by detecting the presence of fluid at the leakage point
- G01M3/12—Investigating 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
〔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)
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.
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)
| 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 |
-
1984
- 1984-08-30 JP JP17945584A patent/JPS6157829A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6157829A (en) | 1986-03-24 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |