JPH0222782B2 - - Google Patents
Info
- Publication number
- JPH0222782B2 JPH0222782B2 JP891782A JP891782A JPH0222782B2 JP H0222782 B2 JPH0222782 B2 JP H0222782B2 JP 891782 A JP891782 A JP 891782A JP 891782 A JP891782 A JP 891782A JP H0222782 B2 JPH0222782 B2 JP H0222782B2
- Authority
- JP
- Japan
- Prior art keywords
- corrosion
- gap
- sealing material
- powder
- preventing sealing
- 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
- 229920001971 elastomer Polymers 0.000 claims description 20
- 239000000463 material Substances 0.000 claims description 20
- 239000005060 rubber Substances 0.000 claims description 20
- 239000003566 sealing material Substances 0.000 claims description 18
- 229910052751 metal Inorganic materials 0.000 claims description 16
- 239000002184 metal Substances 0.000 claims description 16
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical group [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 12
- 239000000843 powder Substances 0.000 claims description 12
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 7
- 229910000861 Mg alloy Inorganic materials 0.000 claims description 5
- SNAAJJQQZSMGQD-UHFFFAOYSA-N aluminum magnesium Chemical compound [Mg].[Al] SNAAJJQQZSMGQD-UHFFFAOYSA-N 0.000 claims description 5
- 239000000395 magnesium oxide Substances 0.000 claims description 4
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 4
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims description 4
- 238000000465 moulding Methods 0.000 claims 1
- 238000005260 corrosion Methods 0.000 description 17
- 230000007797 corrosion Effects 0.000 description 17
- 238000012360 testing method Methods 0.000 description 8
- 239000007788 liquid Substances 0.000 description 7
- 230000000694 effects Effects 0.000 description 6
- 239000013535 sea water Substances 0.000 description 6
- 229910052725 zinc Inorganic materials 0.000 description 4
- 239000011701 zinc Substances 0.000 description 4
- 230000002378 acidificating effect Effects 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 238000007789 sealing Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 238000011534 incubation Methods 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- UGZADUVQMDAIAO-UHFFFAOYSA-L zinc hydroxide Chemical compound [OH-].[OH-].[Zn+2] UGZADUVQMDAIAO-UHFFFAOYSA-L 0.000 description 2
- 229940007718 zinc hydroxide Drugs 0.000 description 2
- 229910021511 zinc hydroxide Inorganic materials 0.000 description 2
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- 229920003319 Araldite® Polymers 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 238000010612 desalination reaction Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000013013 elastic material Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000008235 industrial water Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 238000005057 refrigeration Methods 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
Landscapes
- Sealing Material Composition (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
〔発明の利用分野〕
本発明は海水、淡水化プラント、ポンプ、冷凍
熱、熱交換器およびそれらの配管などのシーリン
グ部分に使用される腐食防止シール材に関するも
のである。
〔発明の背景〕
従来、海水および工業用水などの流体を輸送す
る配管などでは、その接続部はシート状あるいは
リング状のゴム質あるいは石綿などでシーリング
されて微細な隙間を構成している。また一般の機
械および装置におけるボルト締付部分および平面
と平面との接合面も、前記と同様に微細な隙間を
構成している。
上記微細な隙間では、物質の移動が困難である
ため、隙間内の液質中に一定量含有されている溶
存酸素は金属の不働態皮膜の形成に消費されるけ
れども、その補給が困難である欠点がある。
このため隙間内の金属表面(以下隙間内表面と
称す)には、不完全な不働態皮膜のため皮膜に覆
われない金属表面が露出するる恐れがある。一
方、隙間内表面に隣接する外表面は、溶存酸素の
補給が十分に行われているため、金属表面の不働
態皮膜が安定である。
このような状態では、電気化学的に隙間内表面
は液質に対して卑電位を示し、その内表面に隣接
する外表面は貴電位を示すため、隙間内表面と隣
接外表面との間に電位差を生じて隙間内表面が活
性溶解するから、隣接する外表面では隙間内表面
から放出された電荷に対して等価的に溶存酸素の
還元反応(カソード反応)を行うことになる。ま
た隙間内では内表面の溶解により水素イオン濃度
が増加するため、隙間内の液質は酸性に移行す
る。このような状態では、隙間内表面はその不働
態皮膜が不安定となつて溶解するから、隙間腐食
は益益進行する。
上記のように隙間腐食の発生は、隙間内表面が
アノードに、隣接する外表面がカソードにそれぞ
れ分極し、隙間内表面が溶解すると共に、隙間内
の液質が酸性に移行することに基因する。
従来、酸化マグネシウムおよび黒鉛粉末を含有
してなるゴムがあるが(昭和44年7月30日、日刊
工業新聞社発行「ゴム技術ガイドブツク」第191
頁)、これらゴムをシール材として用いても亜鉛
粉末など犠牲陽極となる金属粉末を含有していな
いので腐食防止作用は期待できず、また腐食防止
を目的としたシール材も種々開発されているが
(例えば特開昭52−35230号、特開昭58−5351号)、
いずれも犠牲陽極となる金属粉末は添加されてお
らず、流電防食による作用は期待できない。
〔発明の目的〕
本発明は上記に鑑み、自然の腐食環境のうちで
著大な腐食性を有する海水中の隙間腐食の発生を
長期間にわたつて防止できる腐食防止シール材を
提供することを目的とする。
〔発明の概要〕
本発明の腐食防止シール材はゴム質(ゴム状の
弾性体物質)の基材に犠牲陽極となる金属粉末を
添加し、静電荷を帯電させた黒鉛粉末によつて前
記金属粉末を電気的に結合し、シール材に犠牲陽
極作用を付与したものである。
犠牲陽極となる金属粉末としては、被防食部材
より卑の電極電位を有する金属であればよく、例
えば亜鉛粉末、マグネシウムを30〜60%(重量
比)を含有するアルミニウム−マグネシウム合金
の電極電位は著しく卑電位であり、したがつて流
電防食の対象になりうる材料の範囲は広い。
本発明の腐食防止シール材は、その含有物質が
シーリングされた隙間内表面(隙間内の金属表
面)およびこの内表面に隣接する外表面に対して
優先的に溶解する過程で、隙間内の液質が酸性へ
移行するのを阻止して弱アルカリ性に維持し、隙
間内表面の不働態皮膜を安定にするようにしたも
のである。
上記のようにゴム質の基材に例えば亜鉛粉末を
添加した場合、シーリングされた隙間内表面と、
この隙間内表面に隣接する外表面との間に電位差
を発生させないためである。ゴム質の基材中に添
加して分散された亜鉛は表面近傍において露出し
ているため、この露出亜鉛が隙間内表面と接触す
ると、隙間内表面と隣接する外表面をカソードに
分極し、自らはアノードに分極して溶解する。
このように隙間内表面と隣接する外表面はカソ
ード分極するから、電位差はなくなる。このため
隙間内表面は腐食しないので、隣接する外表面と
共に防食することができる。また亜鉛は金属表面
に優先して溶解し、非晶質の水酸化亜鉛となつて
隙間内に拡散する。同時に隙間内の液質も弱アル
カリ性に移行し、隙間内表面の不働態皮膜を安定
にする。
上記理由によつて亜鉛粉末を添加する場合、そ
の添加量はゴム質の基材に対して重量比で5%以
下では、ゴム質のすきま腐食抑制効果が少なく、
また350%以上ではゴム質の架橋反応が速くなり、
ゴム質基材の弾性を阻害するので5〜350%にす
るのが好ましい。
ゴム質基材において酸化マグネシウムは、亜鉛
が非晶質の水酸化亜鉛となつて溶出するので、亜
鉛粉末を有効に消費させるために、ゴム質基材に
吸湿性を付与する作用がある。前記酸化マグネシ
ウムの添加量は、20%以下では効果が少なく、
100%以上ではゴム質基材の弾性を阻害するから
20〜100%にするのが好ましい。
マグネシウムを30〜60%含有するアルミニウム
−マグネシウム合金の場合も、上記と同様の理由
により5〜200%にするのが好ましい。
静電荷を帯電した黒鉛粉末は、その極性のため
ゴム質基材中で連鎖状につながり、これがゴム質
基材中に分散している犠牲陽極となる金属粉末を
電気的に相互に結合させ、金属粉末を有効に消費
させる作用をする。その添加量は、20%以下では
効果が少なく、200%以上では不経済となるから
20〜200%にするのが好ましい。
前記亜鉛粉末またはアルミニウム−マグネシウ
ム合金粉末および黒鉛粉末がゴム質基材に添加さ
れた場合、シール性を阻害しないためには球状あ
るいは多角形状に形成するのがよく、また均一分
散の観点から微細形状に形成するのが好ましい。
しかも前記粉末の直径は0.1μm以下では不経済で
あり、100μm以上ではシール性を阻害するから
0.1〜100μmにすることが好ましい。
さらにゴム質基材は耐海水性が良好で、かつ海
水中で隙間腐食を生じ難いものとして、ゴム質の
架橋反応を有機系過酸化物、例えばエチレンプロ
ピレン、クロロプレンゴムおよび金属酸化物で行
うものが適している。
〔発明の実施例〕
次に実施例について説明する。
化学組成がC:0.07%、Si:0.56%、Mn:1.31
%、Cr:18.30%、Ni:8.14%である市販のステ
ンレス鋼(SUS304)を加工して円形試験片1を
作り、この試験片1を第1図、第2図に示すよう
に本発明品である供試シール材2(第1表A,B
参照)を介して一体に結合することにより隙間腐
食試験片を組立て、これを50℃の人工海水中に30
日間浸漬し、隙間内電位をポテンシヨメータを測
定すると共に、隙間内の液質変化を調べた。
[Field of Application of the Invention] The present invention relates to a corrosion-preventing sealing material used for sealing parts of seawater, desalination plants, pumps, refrigeration heat, heat exchangers, and their piping. [Background of the Invention] Conventionally, in piping for transporting fluids such as seawater and industrial water, the connecting portions thereof are sealed with a sheet-like or ring-like rubber material, asbestos, or the like to form minute gaps. Furthermore, the bolt tightening portions and the joint surfaces between two planes in general machines and devices also form fine gaps in the same way as described above. Since it is difficult for substances to move in the above-mentioned minute gaps, it is difficult to replenish dissolved oxygen, which is contained in a certain amount in the liquid in the gaps, although it is consumed in the formation of a passive film on the metal. There are drawbacks. For this reason, there is a risk that the metal surface within the gap (hereinafter referred to as the surface within the gap) that is not covered with the film may be exposed due to the incomplete passive film. On the other hand, since the outer surface adjacent to the inner surface of the gap is sufficiently supplied with dissolved oxygen, the passive film on the metal surface is stable. In such a state, electrochemically, the inner surface of the gap exhibits a base potential with respect to the liquid, and the outer surface adjacent to the inner surface exhibits a noble potential, so there is a gap between the inner surface of the gap and the adjacent outer surface. Since a potential difference is generated and the inner surface of the gap is actively dissolved, the adjoining outer surface undergoes a reduction reaction (cathode reaction) of dissolved oxygen equivalent to the charge released from the inner surface of the gap. In addition, since the hydrogen ion concentration increases within the gap due to dissolution of the inner surface, the liquid quality within the gap becomes acidic. In such a state, the passive film on the inner surface of the gap becomes unstable and dissolves, so that crevice corrosion progresses. As mentioned above, the occurrence of crevice corrosion is due to the fact that the inner surface of the crevice is polarized as an anode and the adjacent outer surface is polarized as a cathode, and as the inner surface of the crevice dissolves, the liquid quality within the crevice becomes acidic. . Conventionally, there is rubber containing magnesium oxide and graphite powder (July 30, 1960, "Rubber Technology Guidebook" published by Nikkan Kogyo Shimbun, No. 191)
Page), even if these rubbers are used as sealing materials, they do not contain zinc powder or other metal powders that serve as sacrificial anodes, so they cannot be expected to prevent corrosion, and various sealing materials have been developed for the purpose of preventing corrosion. (For example, JP-A-52-35230, JP-A-58-5351)
In both cases, no metal powder is added to serve as a sacrificial anode, and galvanic corrosion protection cannot be expected. [Object of the Invention] In view of the above, the present invention aims to provide a corrosion-preventing sealing material that can prevent the occurrence of crevice corrosion in seawater, which is a highly corrosive natural environment, for a long period of time. purpose. [Summary of the Invention] The corrosion-preventing sealing material of the present invention has a rubber (rubber-like elastic material) base material added with metal powder to serve as a sacrificial anode, and electrostatically charged graphite powder is used to remove the metal. The powder is electrically bonded to give the sealing material a sacrificial anode effect. The metal powder used as the sacrificial anode may be any metal that has an electrode potential more base than that of the member to be protected; for example, the electrode potential of zinc powder or an aluminum-magnesium alloy containing 30 to 60% magnesium (by weight) is There is a wide range of materials that have a very low potential and can therefore be subject to galvanic protection. The corrosion-preventing sealing material of the present invention dissolves liquid in the gap in a process in which the substance contained therein dissolves preferentially on the sealed gap inner surface (metal surface in the gap) and the outer surface adjacent to this inner surface. This prevents the quality from becoming acidic and maintains it at a slightly alkaline state, thereby stabilizing the passive film on the inner surface of the gap. When, for example, zinc powder is added to the rubber base material as described above, the sealed gap inner surface,
This is to prevent a potential difference from occurring between the inner surface of the gap and the adjacent outer surface. Zinc added and dispersed in the rubber base material is exposed near the surface, so when this exposed zinc comes into contact with the inner surface of the gap, it polarizes the outer surface adjacent to the inner surface of the gap into a cathode, and is polarized and dissolved at the anode. Since the inner surface of the gap and the adjacent outer surface are cathodically polarized in this way, there is no potential difference. Therefore, since the inner surface of the gap does not corrode, it can be protected from corrosion along with the adjacent outer surface. Furthermore, zinc preferentially dissolves on the metal surface, becomes amorphous zinc hydroxide, and diffuses into the gap. At the same time, the liquid quality within the gap also changes to slightly alkaline, which stabilizes the passive film on the surface inside the gap. When adding zinc powder for the above reasons, if the amount added is less than 5% by weight based on the rubber base material, the effect of inhibiting crevice corrosion of the rubber material will be small;
In addition, at 350% or more, the crosslinking reaction of the rubber becomes faster.
Since it inhibits the elasticity of the rubber base material, it is preferably 5 to 350%. In the rubber base material, magnesium oxide dissolves zinc as amorphous zinc hydroxide, so it has the effect of imparting hygroscopicity to the rubber base material in order to effectively consume the zinc powder. If the amount of magnesium oxide added is less than 20%, the effect will be small;
If it exceeds 100%, it will inhibit the elasticity of the rubber base material.
It is preferable to set it to 20-100%. In the case of an aluminum-magnesium alloy containing 30 to 60% magnesium, the content is preferably 5 to 200% for the same reason as above. Due to its polarity, the electrostatically charged graphite powder is chained in the rubber base material, which electrically interconnects the metal powders that serve as sacrificial anodes dispersed in the rubber base material. It works to effectively consume metal powder. If the amount added is less than 20%, it will have little effect, and if it is more than 200%, it will be uneconomical.
It is preferable to set it to 20-200%. When the zinc powder, aluminum-magnesium alloy powder, and graphite powder are added to a rubber base material, it is preferable to form them into a spherical or polygonal shape in order not to impede sealing performance, and from the viewpoint of uniform dispersion, it is preferable to form them into a spherical or polygonal shape. It is preferable to form the
Moreover, if the diameter of the powder is less than 0.1 μm, it is uneconomical, and if it is more than 100 μm, the sealing performance will be impaired.
The thickness is preferably 0.1 to 100 μm. Furthermore, the rubber base material has good seawater resistance and does not easily cause crevice corrosion in seawater, so the crosslinking reaction of the rubber material is performed using organic peroxides such as ethylene propylene, chloroprene rubber, and metal oxides. is suitable. [Embodiments of the Invention] Next, embodiments will be described. Chemical composition: C: 0.07%, Si: 0.56%, Mn: 1.31
%, Cr: 18.30%, Ni: 8.14% commercially available stainless steel (SUS304) was processed to make a circular test piece 1, and this test piece 1 was used as a product of the present invention as shown in Figs. 1 and 2. Test sealing material 2 (Table 1 A, B
Assemble the crevice corrosion test specimens by bonding them together via the
After soaking for a day, the potential within the gap was measured using a potentiometer, and changes in the liquid quality within the gap were investigated.
【表】【table】
【表】
なお図において、3はテフロンチユーブ、4,
5はポテンシヨメータ(図示せず)に接続された
電極、6はシール材(アラルダイト)である。
上記実験の結果、隙間腐食状態は第2表A,B
に示すとおりである。この表中の腐食面積率A
は、隙間内表面積が2512mm2に対する腐食面の占め
る割合である。また潜伏期間(日)は隙間腐食を
発生するまでの期間で、その隙間腐食は隙間端面
から起りやすく、端面に赤褐色のさびが認められ
るので、そのさびの発見日付単位で評価したもの
である。したがつて潜伏期間が30日の場合は腐食
されないことを示す。
〔発明の効果〕
以上説明したように本発明によれば、著大な腐
食性を有する海水中のステンレス鋼、アルミニウ
ム合金などの隙間腐食の発生を長期間にわたつて
防止し、機械および機器類の信頼性の向上をはか
ることが可能な腐食防止シール材を得ることがで
きる。[Table] In the figure, 3 is a Teflon tube, 4,
5 is an electrode connected to a potentiometer (not shown), and 6 is a sealing material (Araldite). As a result of the above experiment, the crevice corrosion state is shown in Table 2 A and B.
As shown below. Corrosion area rate A in this table
is the ratio of the corroded surface to the internal gap surface area of 2512 mm 2 . In addition, the incubation period (days) is the period until crevice corrosion occurs, and since crevice corrosion tends to occur from the edge of the gap, and reddish-brown rust is observed on the edge, the evaluation is based on the date the rust was discovered. Therefore, an incubation period of 30 days indicates no corrosion. [Effects of the Invention] As explained above, according to the present invention, the occurrence of crevice corrosion in stainless steel, aluminum alloy, etc. in highly corrosive seawater can be prevented for a long period of time, and machinery and equipment can be It is possible to obtain a corrosion-preventing sealing material that can improve the reliability of.
第1図、第2図は本発明のシール材を試験する
ための隙間腐食試験片の組立状態を示す図であ
る。
1……試験片、2……供試シール材、4,5…
…電極。
FIGS. 1 and 2 are diagrams showing the assembled state of a crevice corrosion test piece for testing the sealing material of the present invention. 1... Test piece, 2... Test sealing material, 4, 5...
…electrode.
Claims (1)
粉末を添加し成形してなる腐食防止シール材にお
いて、基材に犠牲陽極となる金属粉末を添加し、
黒鉛粉末に静電荷を帯電させて前記金属粉末を電
気的に結合してなることを特徴とする腐食防止シ
ール材。 2 犠牲陽極となる金属粉末が亜鉛粉末であるこ
とを特徴とする特許請求の範囲第1項記載の腐食
防止シール材。 3 亜鉛粉末を5〜350%(重量比)添加するこ
とを特徴とする特許請求の範囲第2項記載の腐食
防止シール材。 4 犠牲陽極となる物質がアルミニウム−マグネ
シウム合金であることを特徴とする特許請求の範
囲第1項記載の腐食防止シール材。 5 アルミニウム−マグネシウム合金を5〜200
%(重量比)添加することを特徴とする特許請求
の範囲第4項記載の腐食防止シール材。[Scope of Claims] 1. A corrosion-preventing sealing material formed by adding magnesium oxide and graphite powder to a rubber base material and molding the material, in which a metal powder serving as a sacrificial anode is added to the base material,
A corrosion-preventing sealing material characterized in that graphite powder is electrostatically charged and the metal powder is electrically bonded to the graphite powder. 2. The corrosion-preventing sealing material according to claim 1, wherein the metal powder serving as the sacrificial anode is zinc powder. 3. The corrosion-preventing sealing material according to claim 2, wherein 5 to 350% (weight ratio) of zinc powder is added. 4. The corrosion-preventing sealing material according to claim 1, wherein the material serving as the sacrificial anode is an aluminum-magnesium alloy. 5 Aluminum-magnesium alloy from 5 to 200
% (weight ratio) of the corrosion-preventing sealing material according to claim 4.
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP891782A JPS58127747A (en) | 1982-01-25 | 1982-01-25 | Corrosion-inhibiting sealing material |
| EP83100543A EP0090912B1 (en) | 1982-01-25 | 1983-01-21 | Anti-crevice corrosion sealant, and method of using it |
| DE8383100543T DE3376336D1 (en) | 1982-01-25 | 1983-01-21 | Anti-crevice corrosion sealant, and method of using it |
| US06/460,017 US4433093A (en) | 1982-01-25 | 1983-01-21 | Anti-crevice corrosion sealant and method for anti-crevice corrosion |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP891782A JPS58127747A (en) | 1982-01-25 | 1982-01-25 | Corrosion-inhibiting sealing material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58127747A JPS58127747A (en) | 1983-07-29 |
| JPH0222782B2 true JPH0222782B2 (en) | 1990-05-21 |
Family
ID=11706002
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP891782A Granted JPS58127747A (en) | 1982-01-25 | 1982-01-25 | Corrosion-inhibiting sealing material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58127747A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5331349B2 (en) * | 2008-02-08 | 2013-10-30 | アサヒゴム株式会社 | Plastisol sealant composition |
-
1982
- 1982-01-25 JP JP891782A patent/JPS58127747A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58127747A (en) | 1983-07-29 |
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