JPS6360280B2 - - Google Patents
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- Publication number
- JPS6360280B2 JPS6360280B2 JP22007282A JP22007282A JPS6360280B2 JP S6360280 B2 JPS6360280 B2 JP S6360280B2 JP 22007282 A JP22007282 A JP 22007282A JP 22007282 A JP22007282 A JP 22007282A JP S6360280 B2 JPS6360280 B2 JP S6360280B2
- Authority
- JP
- Japan
- Prior art keywords
- parts
- weight
- layer
- pipe
- corrosion
- 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
- 239000000463 material Substances 0.000 claims description 20
- 230000002093 peripheral effect Effects 0.000 claims description 18
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 17
- 239000011701 zinc Substances 0.000 claims description 13
- 229910052725 zinc Inorganic materials 0.000 claims description 11
- 239000000843 powder Substances 0.000 claims description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 7
- 238000009413 insulation Methods 0.000 claims description 6
- 239000000395 magnesium oxide Substances 0.000 claims description 6
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 6
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims description 6
- 239000010935 stainless steel Substances 0.000 claims description 5
- 229910001220 stainless steel Inorganic materials 0.000 claims description 5
- 229910000975 Carbon steel Inorganic materials 0.000 claims description 3
- 229910052782 aluminium Inorganic materials 0.000 claims description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 239000010962 carbon steel Substances 0.000 claims description 3
- 238000010073 coating (rubber) Methods 0.000 claims description 3
- 239000010696 ester oil Substances 0.000 claims description 3
- 239000011810 insulating material Substances 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- 229920000642 polymer Polymers 0.000 claims description 3
- 239000010410 layer Substances 0.000 description 62
- 238000005260 corrosion Methods 0.000 description 33
- 230000007797 corrosion Effects 0.000 description 20
- 229910052751 metal Inorganic materials 0.000 description 15
- 239000002184 metal Substances 0.000 description 15
- 239000004744 fabric Substances 0.000 description 12
- 230000000694 effects Effects 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 239000011247 coating layer Substances 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- -1 polyethylene Polymers 0.000 description 4
- 238000004090 dissolution Methods 0.000 description 3
- 239000000523 sample Substances 0.000 description 3
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 239000010425 asbestos Substances 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 229910052895 riebeckite Inorganic materials 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 239000004809 Teflon Substances 0.000 description 1
- 229920006362 Teflon® Polymers 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000006056 electrooxidation reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000006353 environmental stress Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 230000017525 heat dissipation Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 230000010287 polarization Effects 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- 230000032258 transport Effects 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
Landscapes
- Protection Of Pipes Against Damage, Friction, And Corrosion (AREA)
- Thermal Insulation (AREA)
- Prevention Of Electric Corrosion (AREA)
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は高温水および蒸気などを輸送するのに
用いられる被覆配管に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to coated piping used for transporting high temperature water, steam, and the like.
従来のこの種被覆配管は第1図に示すように、
配管1の外周面を断熱材、例えばアスベスト繊維
布、シリカ繊維布などを積層させた保温層3によ
り被覆し、さらにこの保温層3の外周面を防水材
例えばアルミニウム、ステンレス鋼、炭素鋼など
の薄肉の金属板、またはナイロン、ビニール、ポ
リエチレンなどの合成樹脂製シートからなる防水
層4により被覆して構成されている。
Conventional covered piping of this type is shown in Figure 1.
The outer circumferential surface of the pipe 1 is covered with a heat insulating layer 3 made of laminated heat insulating material such as asbestos fiber cloth, silica fiber cloth, etc., and the outer circumferential surface of this heat insulating layer 3 is covered with a waterproof material such as aluminum, stainless steel, carbon steel, etc. It is covered with a waterproof layer 4 made of a thin metal plate or a synthetic resin sheet such as nylon, vinyl, or polyethylene.
上記のように配管1を保温層3および防水層4
により2重に被覆しても、その配管1の外周面は
外界の環境から完全に遮断されているわけではな
く、大気が防水層4および保温層3を形成する材
料の微細な隙間または空間を流通して配管1の外
周面に到達する。このため大気中に含まれた水分
(温度)は、配管1の表面の冷熱サイクルの過程
において結露し、その表面に付着するから電気化
学的に腐食反応が起りやすい状態となる。さらに
前記保温層3を形成するアスベスト繊維布、シリ
カ繊維布などから腐食性の塩素イオンなどが溶出
し、配管1の外周表面の不働態皮膜を破壊して腐
食現象を生ずる恐れがある。
As shown above, connect piping 1 to heat insulation layer 3 and waterproof layer 4.
Even if the pipe 1 is coated with double layers, the outer peripheral surface of the pipe 1 is not completely shielded from the outside environment. It flows and reaches the outer circumferential surface of the pipe 1. Therefore, moisture (temperature) contained in the atmosphere condenses on the surface of the pipe 1 during the cooling and heating cycle and adheres to the surface, making it easy for electrochemical corrosion reactions to occur. Furthermore, corrosive chlorine ions and the like are eluted from asbestos fiber cloth, silica fiber cloth, etc. forming the heat insulating layer 3, and there is a fear that the passive film on the outer circumferential surface of the pipe 1 may be destroyed and a corrosion phenomenon may occur.
上記腐食現象は、炭素鋼製被覆配管では全面腐
食状態となり、またステンレス製被覆配管では孔
食状態となる傾向がある。特に高温水および蒸気
などを輸送するステンレス鋼製被覆配管では、腐
食性環境と熱応力が相乗的に影響するため、配管
の外周表面から応力腐食割れを発生する恐れがあ
る。また被覆配管の最外側の被覆層すなわち防水
層4が金属体で形成されている場合には、その金
属体の内側面すなわち保温層3に接合する表面が
上記と同様に腐食して損傷する恐れがある。 The above-mentioned corrosion phenomenon tends to result in general corrosion in carbon steel coated pipes, and pitting corrosion in stainless steel coated pipes. In particular, in coated stainless steel piping that transports high-temperature water and steam, there is a risk that stress corrosion cracking may occur from the outer surface of the piping due to the synergistic effect of a corrosive environment and thermal stress. In addition, if the outermost coating layer of the covered pipe, that is, the waterproof layer 4, is formed of a metal body, the inner surface of the metal body, that is, the surface that is bonded to the heat insulating layer 3, may be corroded and damaged in the same manner as described above. There is.
本発明は上記にかんがみ保温層を設けた配管の
外周面および最外側の防水層の金属体の内面の腐
食を防止し、長寿命の被覆配管を提供することを
目的とする。 In view of the above, an object of the present invention is to prevent corrosion of the outer circumferential surface of a pipe provided with a heat insulating layer and the inner surface of the metal body of the outermost waterproof layer, and to provide a long-life coated pipe.
本発明は上記目的を達成するために、配管の外
周面に断熱材よりなる保温層を設け、この保温層
の外周面に防水材よりなる防水層を設けた被覆配
管において、ゴム質基材100重量部、亜鉛微粉末
5〜350重量部、静電荷を帯電した炭素微粉末10
〜20重量部および酸化マグネシウム微粉末20〜
100重量部からなるゴム質被覆材の防食層を、前
記配管の外周面上に設けることにより達成され
る。
In order to achieve the above object, the present invention provides a coated pipe in which a heat insulation layer made of a heat insulating material is provided on the outer peripheral surface of the pipe, and a waterproof layer made of a waterproof material is provided on the outer peripheral surface of this heat insulation layer. Parts by weight, 5 to 350 parts by weight of zinc fine powder, 10 parts by weight of electrostatically charged carbon fine powder
~20 parts by weight and 20~ fine magnesium oxide powder
This is achieved by providing an anti-corrosion layer of 100 parts by weight of a rubber coating material on the outer peripheral surface of the pipe.
防食層中の亜鉛がアノード側に分極し、配管の
金属表面の溶解反応を防いで配管を防食する。炭
素微粉末及び酸化マグネシウム微粉末は亜鉛を有
効に消費するのに役立つ。又、最外側の防水層は
防食層の防食機能および保温層の断熱作用を長期
間維持するために役立つている。
Zinc in the anti-corrosion layer is polarized to the anode side, preventing a dissolution reaction on the metal surface of the pipe and preventing corrosion of the pipe. Fine carbon powder and fine magnesium oxide powder help consume zinc effectively. In addition, the outermost waterproof layer serves to maintain the anti-corrosion function of the anti-corrosion layer and the insulation effect of the heat-retaining layer for a long period of time.
以下本発明の実施例を図面について説明する。 Embodiments of the present invention will be described below with reference to the drawings.
第2図において、1は高温水および蒸気などを
輸送する配管で、この配管1の外周面は防食層2
により被覆されている。この防食層2は、ゴム質
基材100重量部、亜鉛微粉末5〜350重量部、静電
荷を帯電した炭素微粉末10〜200重量部および酸
化マグネシウム微粉末20〜100重量部からなるゴ
ム質被覆材により形成されている。前記ゴム質基
材は、配管1内を流通する流体の高温度に対し、
その耐熱性を考慮して選定される。3は前記防食
層2の外周面を被覆する保温層、4はこの保温層
3の外周面を被覆する防水層で、この防水層4お
よび前記保温層3は第1図に示す従来例と同様に
形成されるので、その説明を省略する。 In Fig. 2, 1 is a pipe for transporting high-temperature water, steam, etc., and the outer peripheral surface of this pipe 1 is coated with a corrosion protection layer 2.
covered with. This anti-corrosion layer 2 is made of a rubber material consisting of 100 parts by weight of a rubber base material, 5 to 350 parts by weight of zinc fine powder, 10 to 200 parts by weight of electrostatically charged carbon fine powder, and 20 to 100 parts by weight of magnesium oxide fine powder. It is formed from a covering material. The rubber base material resists the high temperature of the fluid flowing through the pipe 1.
It is selected considering its heat resistance. 3 is a heat insulating layer that covers the outer peripheral surface of the anticorrosive layer 2; 4 is a waterproof layer that covers the outer peripheral surface of the heat insulating layer 3; this waterproof layer 4 and the heat insulating layer 3 are similar to the conventional example shown in FIG. , so its explanation will be omitted.
次に上記各被覆層の機能について説明する。 Next, the functions of each of the above-mentioned coating layers will be explained.
まず防食層2はゴム質基材中に帯電性を有する
炭素微粉末を分散させることにより、ゴム生地に
導電性を付与することができる。ゴム質基材中に
亜鉛微粉末を添加することにより、ゴム質が金属
表面に接触すると、亜鉛粉末がゴム生地を電気導
体としてアノード分極しやすくする。 First, the anticorrosion layer 2 can impart electrical conductivity to the rubber fabric by dispersing fine carbon powder having chargeability in the rubber base material. By adding fine zinc powder to the rubber base material, when the rubber material comes into contact with a metal surface, the zinc powder makes the rubber fabric an electrical conductor and facilitates anodic polarization.
いま前記ゴム質被覆材を帯状に形成し、この帯
状体を配管1の外周面に巻回して防食層2を形成
すると、前記帯状体間より結露水が内部に侵入
し、配管1の外周面と防食層2との間に滞留す
る。このため配管1の金属表面(主として鉄表
面)の水溶液に対する電極電位は、ゴム生地中に
分岐している亜鉛の電極電位よりも貴電位系列に
位置するので、亜鉛はゴム生地を電気導体として
アノード側に分極し、下記(1)式に示す溶解反応を
行う。 Now, when the rubber coating material is formed into a strip and this strip is wound around the outer circumferential surface of the pipe 1 to form the anticorrosion layer 2, condensed water will enter the interior from between the strips and the outer circumferential surface of the pipe 1. and the corrosion protection layer 2. Therefore, the electrode potential of the metal surface (mainly the iron surface) of the pipe 1 with respect to the aqueous solution is located in the more noble potential series than the electrode potential of zinc branched in the rubber fabric, so zinc is used as an anode with the rubber fabric as an electrical conductor. The dissolution reaction shown in equation (1) below is performed.
Zn→Zn2++2e ……(1)
また配管1の金属表面では、上記(1)式のアード
反応により放出される電子と等価的に下記(2)式の
カソード反応が行われるので、前記金属表面自体
の溶解反応は起らず防食される。 Zn→Zn 2+ +2e ...(1) Also, on the metal surface of the pipe 1, the cathode reaction of the following formula (2) takes place, which is equivalent to the electrons released by the Ard reaction of the formula (1) above. No dissolution reaction occurs on the metal surface itself, and corrosion is prevented.
H2O+1/2O2+2e→2OH ……(2)
一方、亜鉛の溶解過程では液質を弱ルカリ性と
するため、配管の金属表面の不働態は保持される
から、その金属表面をほぼ完全な防食状態に維持
することができる。 H 2 O + 1/2O 2 + 2e → 2OH ... (2) On the other hand, in the process of dissolving zinc, the liquid quality is made weakly alkaline, so the passivity of the metal surface of the pipe is maintained, so the metal surface is almost completely It can be maintained in a corrosion-proof state.
さらに配管1の外周面からの熱伝達により、熱
放散はゴム質により抑制されるが、このゴム生地
では固体熱伝達となるから保温層3が必要であ
る。この保温層3は、熱伝導性の悪い空気を利用
するため、空間体積の多いシリカガラス繊維、発
泡ウレタンおよびポリスチレン樹脂などを主体と
して積層状に構成されている。これらの樹脂層か
ら前記結露現象により腐食要因となる塩素イオン
などのカチオンが溶出しても、このカチオンは防
食層1のゴム質最外層部において亜鉛により捕捉
され、塩化亜鉛となつてたまるから配管1の外周
面に到達する恐れはない。 Furthermore, heat dissipation due to heat transfer from the outer circumferential surface of the pipe 1 is suppressed by the rubber material, but since this rubber fabric results in solid heat transfer, the heat insulating layer 3 is necessary. In order to utilize air with poor thermal conductivity, the heat insulating layer 3 is constructed in a laminated form mainly of silica glass fiber, foamed urethane, polystyrene resin, etc., each having a large space volume. Even if cations such as chlorine ions, which cause corrosion, are eluted from these resin layers due to the aforementioned dew condensation phenomenon, these cations are captured by zinc in the rubbery outermost layer of the anti-corrosion layer 1 and accumulate as zinc chloride. There is no possibility that the outer peripheral surface of No. 1 will be reached.
最外側の防水層4は、前記防食層2の防食機能
および保温層3の断熱作用を長期間維持するため
に必要な被覆層である。この防水層4が金属体で
あるときには、機械強度の面では安定しているけ
れども、腐食による損傷が考えられるから内側表
面に防食処理を施す必要がある。すなわち防水層
4がアルミニウムまたはステンレス鋼よりなる場
合には、ポリブデンを主体とするポリマー100重
量部に亜鉛微粉末:30〜50重量部および静電荷を
滞電したエステル油:20〜200重量部からなる混
合物の層を、前記金属体の内周面または保温層3
の外周面に設けて隙間腐食の発生を抑制する。 The outermost waterproof layer 4 is a coating layer necessary to maintain the anticorrosive function of the anticorrosive layer 2 and the heat insulating effect of the heat insulating layer 3 for a long period of time. When the waterproof layer 4 is a metal body, it is stable in terms of mechanical strength, but it is possible that it will be damaged by corrosion, so it is necessary to apply anti-corrosion treatment to the inner surface. That is, when the waterproof layer 4 is made of aluminum or stainless steel, 100 parts by weight of a polymer mainly composed of polybdenum, 30 to 50 parts by weight of fine zinc powder, and 20 to 200 parts by weight of ester oil charged with static charge. A layer of a mixture of
Provided on the outer peripheral surface of the pipe to suppress the occurrence of crevice corrosion.
一方、防水層4が合成樹脂よりなる場合には、
腐食に対して抵抗力があるけれども、機械的強度
が低く、かつ紫外線による劣化が考えられるの
で、適当な時期に新しいものと交換する必要があ
る。 On the other hand, when the waterproof layer 4 is made of synthetic resin,
Although it is resistant to corrosion, it has low mechanical strength and is susceptible to deterioration due to ultraviolet rays, so it is necessary to replace it with a new one at an appropriate time.
次に防食層2および防水層4を形成する成分組
成の限定理由について説明する。 Next, the reasons for limiting the component compositions forming the anticorrosion layer 2 and the waterproof layer 4 will be explained.
防食層2において、ゴム生地に対する亜鉛微粉
末の量は、ゴム質基材100重量部に対して5重量
部以下では防食効果を持続することができず、
350重量部以上ではゴム質が脆化するから5〜350
重量部に限定した。 In the anti-corrosion layer 2, if the amount of fine zinc powder relative to the rubber fabric is less than 5 parts by weight per 100 parts by weight of the rubber base material, the anti-corrosion effect cannot be maintained;
If it exceeds 350 parts by weight, the rubber will become brittle, so 5 to 350 parts by weight.
Limited to parts by weight.
また静電荷を滞電した炭素微粉末は相互に吸着
する作用を有し、鎖状に接続してゴム生成に分散
するから導電性を付与するが、10重量部以下では
効果がなく、200重量部以上ではゴム生地が脆化
されるから、炭素微粉末の添加量を10〜200重量
部に限定した。 In addition, fine carbon powder with static charges has the effect of adsorbing each other and is connected in a chain and dispersed in the rubber formation, imparting conductivity, but it has no effect when it is less than 10 parts by weight, and when it is less than 200 parts by weight. The amount of fine carbon powder added was limited to 10 to 200 parts by weight since the rubber fabric would become brittle if the amount exceeded 100 parts by weight.
さらに酸化マグネシウムは防食層2の電気化学
的作用を促進させるために必要な適度の吸湿作用
を行うのに有効であり、その添加量はゴム質基材
100重量部に対して20重量部以下では効果がなく、
100重量部以上ではゴム生地が脆化されるから20
〜10部に限定した。 Furthermore, magnesium oxide is effective in performing the appropriate moisture absorption action necessary to promote the electrochemical action of the anti-corrosion layer 2, and the amount of magnesium oxide added is
It has no effect if it is less than 20 parts by weight per 100 parts by weight.
If it exceeds 100 parts by weight, the rubber fabric becomes brittle, so 20
~Limited to 10 copies.
前記のように防水層4が金属体からなる場合に
は、その金属体の内周面または保温層3の外周面
に設ける層はポリブデンポリマー100重量部に添
加する亜鉛微粉末は、30重量部以下では効果がな
く、350重量部以上では作業性が悪化するから、
添加量を30〜350重量部に限定した。前記添加亜
鉛を効果的に消費させるために添加されるエステ
ル油の添加量は、ゴム質基材100重量部に対して
20重量部以上では効果が少なく、200重量部以上
では腐食性を示すから20〜200重量部に限定した。 When the waterproof layer 4 is made of a metal body as described above, the layer provided on the inner peripheral surface of the metal body or the outer peripheral surface of the heat insulating layer 3 contains 30 parts by weight of fine zinc powder added to 100 parts by weight of polybdenum polymer. If it is less than 350 parts by weight, it will not be effective, and if it exceeds 350 parts by weight, workability will deteriorate.
The amount added was limited to 30 to 350 parts by weight. The amount of ester oil added to effectively consume the added zinc is 100 parts by weight of the rubber base material.
If it is more than 20 parts by weight, the effect will be small, and if it is more than 200 parts by weight, it will be corrosive, so it was limited to 20 to 200 parts by weight.
上述したように本実施例は、配管1を防食層
2、保温層3および防水層4により順次に被覆し
たものについて述べたが、本発明はこれに限定さ
れず、配管1を防食層2および防水層4により順
次に被覆してもよいことはもちろんである。 As described above, in this embodiment, the pipe 1 is coated with the anti-corrosion layer 2, the heat-retaining layer 3, and the waterproof layer 4 in this order, but the present invention is not limited to this, and the pipe 1 is coated with the anti-corrosion layer 2 and the waterproof layer 4. Of course, the waterproof layer 4 may be sequentially coated.
次に第3図に示す実施例について説明する。 Next, the embodiment shown in FIG. 3 will be described.
供試材として前述した第1図および第2図に示
す従来の被覆配管Aおよび本発明に係わる被覆配
管Bを用い、この両供試材A,Bの保温層3の断
熱材中に蒸溜水を注入した後、第3図に示すよう
にボルト5、ナツト6およびシールリング7を介
して一体に結合し、この結合した両供試材A,B
をポンプおよび貯水槽(図示せず)に接続して閉
ループ試験装置を構成する。 The conventional coated piping A and the coated piping B according to the present invention shown in FIGS. After injecting, as shown in FIG. 3, the bolts 5, nuts 6, and seal rings 7 are used to connect the two test materials A and B.
is connected to a pump and a water reservoir (not shown) to form a closed-loop test apparatus.
上記供試材A,BのSUS304製配管1内に約80
℃の温水と冷却とを交互に循環させ、配管1の外
周面を交互に加熱、冷却させる。そして725,
1450,1920時間毎に分解して両配管1の各外周面
の状態を調査した。その結果、防食層2を有しな
い供試材Aの配管1外周面には孔食状の隙間腐食
を発生したが、これに反し防食層2を有する供試
材Bの配管1外周面には腐食損傷は全然認められ
ず、防食されていることが確認された。 Approximately 80 mm inside the SUS304 pipe 1 of the above sample materials A and B.
C warm water and cooling are alternately circulated to alternately heat and cool the outer peripheral surface of the pipe 1. and 725,
The pipes 1 were disassembled every 1,450 and 1,920 hours, and the condition of each outer peripheral surface of both pipes 1 was investigated. As a result, pitting-like crevice corrosion occurred on the outer circumferential surface of the pipe 1 of sample material A, which does not have the anticorrosive layer 2, but on the contrary, on the outer circumferential surface of the pipe 1 of sample material B, which has the anticorrosion layer 2. No corrosion damage was observed, confirming that corrosion protection was achieved.
第4図は第3図の被覆配管Bの防食層2におけ
る隙間内の液質のPHおよび隙間内表面の電極電位
の状態を調べる測定装置で、第4図ロは本発明に
係わる防食層2と同質材からなる試験片b、また
は市販のゴム(ニトリルブタジエン)からなる試
験片b′でこの試験片b,b′は3%食塩水(50℃)
中で60日間浸漬したものである。第4図イ,ハは
試験片bの保持部材、第4図ニは組立状態をそれ
ぞれ示す。第4図ニにおける9〜11はテフロン
パイプ、綿糸およびSUS304製電極をそれぞれ示
し、その電極11はポテンシヨスタツトに接続し
て測定する。また隙間内液質のPHは第4図ニに示
す組立状態を分解した後、残留液をPH紙により測
定した。 FIG. 4 shows a measuring device for measuring the pH of the liquid in the gap in the anti-corrosion layer 2 of the covered pipe B in FIG. 3 and the state of the electrode potential on the surface inside the gap. FIG. Test piece b made of the same material as , or test piece b' made of commercially available rubber (nitrile butadiene).These test pieces b and b' were prepared in 3% saline solution (50℃).
It was soaked in water for 60 days. 4A and 4C show the holding member for the test piece b, and FIG. 4D shows the assembled state, respectively. Reference numerals 9 to 11 in FIG. 4D indicate a Teflon pipe, a cotton thread, and an electrode made of SUS304, respectively, and the electrode 11 is connected to a potentiostat for measurement. The PH of the liquid in the gap was determined by disassembling the assembled state shown in FIG. 4D, and then measuring the residual liquid using PH paper.
その結果、本発明に係わる試験片bおよび従来
例の試験片b′を使用した場合の隙間内のPHは、第
5図のC,D線にそれぞれ示すとおりである。す
なわち隙間内のPHは、本発明に係わる試験片bの
場合C線では、漸次弱アルカリ性を示すが、従来
例の試験片b′の場合D線では、漸次酸性を示して
腐食性となることが容易に理解される。 As a result, the PH in the gap when using the test piece b according to the present invention and the conventional test piece b' is as shown by lines C and D in FIG. 5, respectively. In other words, the PH in the gap gradually becomes weakly alkaline at line C for test piece b according to the present invention, but gradually becomes acidic and corrosive at line D for test piece b' of the conventional example. is easily understood.
また本発明に係わる試験片bおよび従来例の試
験片b′を使用した場合の隙間内の電位は、第6図
のE,F線にそれぞれ示すとおりである。すなわ
ち本発明に係わる試験片bの場合E線の電位は、
従来例の試験片b′の場合F線の電位よりも大幅に
卑電位に分極する。したがつて前者では亜鉛によ
りカソード分極されるから、防食されることが容
易に理解される。 Further, the potentials within the gap when using the test piece b according to the present invention and the conventional test piece b' are as shown by lines E and F in FIG. 6, respectively. That is, in the case of test piece b according to the present invention, the potential of the E line is:
In the case of the conventional test piece b', it is polarized to a much more base potential than the F line potential. Therefore, it is easily understood that the former is cathodically polarized by zinc and is therefore protected against corrosion.
以上説明したように本発明によれば、被覆層を
設けた配管の外周面および最外側の防水金属体の
内周面の防食を防止することにより、配管の寿命
を大幅に延長させることができる。
As explained above, according to the present invention, the life of the piping can be significantly extended by preventing corrosion of the outer peripheral surface of the piping provided with the coating layer and the inner peripheral surface of the outermost waterproof metal body. .
第1図は従来の被覆配管の断面図、第2図は本
発明被覆配管の一実施例を示す断面図、第3図は
従来品および本発明品の実験例を示す断面図、第
4図イ〜ハおよびニは防食層の隙間内の液体のPH
と隙間内表面の電極電位を測定する部品およびそ
れらの組立状態を示す断面図、第5図および第6
図は従来品と本発明品の特性を示す説明図であ
る。
1……配管、2……防食層、3……保温層、4
……防水層。
Fig. 1 is a cross-sectional view of a conventional covered pipe, Fig. 2 is a cross-sectional view showing an example of the covered pipe of the present invention, Fig. 3 is a cross-sectional view showing an experimental example of a conventional product and a product of the present invention, and Fig. 4. A to C and D are the pH values of the liquid in the gaps in the anticorrosion layer.
Figures 5 and 6 are cross-sectional views showing parts for measuring the electrode potential on the inner surface of the gap and their assembled state.
The figure is an explanatory diagram showing the characteristics of the conventional product and the product of the present invention. 1... Piping, 2... Corrosion protection layer, 3... Heat retention layer, 4
...Waterproof layer.
Claims (1)
け、この保温層の外周面に防水材よりなる防水層
を設けた被覆配管において、ゴム質基材100重量
部、亜鉛微粉末5〜350重量部、静電荷を帯電し
た炭素微粉末10〜200重量部および酸化マグネシ
ウム微粉末20〜100重量部からなるゴム質被覆材
の防食層を、前記配管の外周面上に設けたことを
特徴とする被覆配管。 2 前記防水層がアルミニウム、ステンレス鋼お
よび炭素鋼のうちいずれか一つの金属材料である
場合に、ポリブデンポリマー100重量部、亜鉛微
粉末30〜350重量部および静電荷を帯電したエス
テル油類20〜200重量部からなる混合物の層を、
前記防水層の内面または保温層の外周面に設けた
ことを特徴とする特許請求の範囲第1項記載の被
覆配管。[Scope of Claims] 1. In a covered pipe in which a heat insulation layer made of a heat insulating material is provided on the outer peripheral surface of the pipe, and a waterproof layer made of a waterproof material is provided on the outer peripheral surface of this heat insulation layer, 100 parts by weight of a rubber base material, zinc An anticorrosive layer of a rubber coating material consisting of 5 to 350 parts by weight of fine powder, 10 to 200 parts by weight of electrostatically charged carbon fine powder, and 20 to 100 parts by weight of magnesium oxide fine powder is provided on the outer peripheral surface of the pipe. Covered piping characterized by: 2. When the waterproof layer is made of any one of aluminum, stainless steel, and carbon steel, 100 parts by weight of polybdenum polymer, 30 to 350 parts by weight of fine zinc powder, and 20 to 20 parts of electrostatically charged ester oil. A layer of a mixture consisting of 200 parts by weight,
The coated pipe according to claim 1, characterized in that it is provided on the inner surface of the waterproof layer or on the outer circumferential surface of the heat insulating layer.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP22007282A JPS59110996A (en) | 1982-12-17 | 1982-12-17 | Coating piping |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP22007282A JPS59110996A (en) | 1982-12-17 | 1982-12-17 | Coating piping |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59110996A JPS59110996A (en) | 1984-06-27 |
| JPS6360280B2 true JPS6360280B2 (en) | 1988-11-24 |
Family
ID=16745500
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP22007282A Granted JPS59110996A (en) | 1982-12-17 | 1982-12-17 | Coating piping |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59110996A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH03100379U (en) * | 1990-01-31 | 1991-10-21 |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002048295A (en) * | 2000-08-03 | 2002-02-15 | Inoac Corp | Piping cover member |
-
1982
- 1982-12-17 JP JP22007282A patent/JPS59110996A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH03100379U (en) * | 1990-01-31 | 1991-10-21 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59110996A (en) | 1984-06-27 |
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