JPS6151986B2 - - Google Patents
Info
- Publication number
- JPS6151986B2 JPS6151986B2 JP12167483A JP12167483A JPS6151986B2 JP S6151986 B2 JPS6151986 B2 JP S6151986B2 JP 12167483 A JP12167483 A JP 12167483A JP 12167483 A JP12167483 A JP 12167483A JP S6151986 B2 JPS6151986 B2 JP S6151986B2
- Authority
- JP
- Japan
- Prior art keywords
- polyolefin
- antifouling
- coating
- eva
- antifouling 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
- 229920000098 polyolefin Polymers 0.000 claims description 32
- 238000000576 coating method Methods 0.000 claims description 21
- 239000002519 antifouling agent Substances 0.000 claims description 19
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 18
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 18
- 239000011248 coating agent Substances 0.000 claims description 17
- 230000003373 anti-fouling effect Effects 0.000 claims description 13
- 239000010410 layer Substances 0.000 description 14
- -1 polyethylene Polymers 0.000 description 9
- 239000004698 Polyethylene Substances 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 229920000573 polyethylene Polymers 0.000 description 7
- 229910000831 Steel Inorganic materials 0.000 description 5
- 235000015170 shellfish Nutrition 0.000 description 5
- 239000010959 steel Substances 0.000 description 5
- 230000007774 longterm Effects 0.000 description 3
- 239000003973 paint Substances 0.000 description 3
- 239000013535 sea water Substances 0.000 description 3
- 241000195493 Cryptophyta Species 0.000 description 2
- APQHKWPGGHMYKJ-UHFFFAOYSA-N Tributyltin oxide Chemical compound CCCC[Sn](CCCC)(CCCC)O[Sn](CCCC)(CCCC)CCCC APQHKWPGGHMYKJ-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical group CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 238000007751 thermal spraying Methods 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- 229920002160 Celluloid Polymers 0.000 description 1
- 241000195628 Chlorophyta Species 0.000 description 1
- 241000238586 Cirripedia Species 0.000 description 1
- 239000005749 Copper compound Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 206010040844 Skin exfoliation Diseases 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 239000003429 antifungal agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 150000001880 copper compounds Chemical class 0.000 description 1
- BERDEBHAJNAUOM-UHFFFAOYSA-N copper(I) oxide Inorganic materials [Cu]O[Cu] BERDEBHAJNAUOM-UHFFFAOYSA-N 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- KRFJLUBVMFXRPN-UHFFFAOYSA-N cuprous oxide Chemical compound [O-2].[Cu+].[Cu+] KRFJLUBVMFXRPN-UHFFFAOYSA-N 0.000 description 1
- 229940112669 cuprous oxide Drugs 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- BFWMWWXRWVJXSE-UHFFFAOYSA-M fentin hydroxide Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(O)C1=CC=CC=C1 BFWMWWXRWVJXSE-UHFFFAOYSA-M 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229920001748 polybutylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 238000012958 reprocessing Methods 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
- 239000004308 thiabendazole Substances 0.000 description 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
- 229960004546 thiabendazole Drugs 0.000 description 1
- 235000010296 thiabendazole Nutrition 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
- Laminated Bodies (AREA)
- Lining Or Joining Of Plastics Or The Like (AREA)
Description
【発明の詳細な説明】
本発明は防汚性を有するポリオレフイン被覆に
関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a polyolefin coating having antifouling properties.
ポリオレフイン被覆、特にポリエチレン被覆は
埋設鋼管の外面或いは海水取水管の内面等に施さ
れ、長年に亘つて優れた防食性能を発揮してい
る。又最近は鋼管杭の防食にも利用され始めてい
る。ポリオレフインは防食性、耐久性が優れてい
るのみならず、上記のような海水に接する用途に
於て貝や藻類の付着も少ないという利点がある。
しかしながらこのように物が付着し難いというポ
リオレフインの性質は一方ではむしろ弱点として
働くものである。たとえばポリオレフイン上に塗
装を施しても、その付着力は弱く、長期の耐久性
を期待できるものではない。 Polyolefin coatings, particularly polyethylene coatings, are applied to the outer surfaces of buried steel pipes or the inner surfaces of seawater intake pipes, and have demonstrated excellent anticorrosion performance for many years. Recently, it has also begun to be used for corrosion protection of steel pipe piles. Polyolefin not only has excellent anticorrosion properties and durability, but also has the advantage of less adhesion of shellfish and algae when used in contact with seawater as mentioned above.
However, the property of polyolefin that substances are difficult to adhere to it actually acts as a weakness. For example, even if paint is applied to polyolefin, its adhesion is weak and long-term durability cannot be expected.
ここで海水取水管に例をとれば、内面にポリオ
レフインを被覆することにより防食効果は十分で
あり、通常は貝類も殆ど付着しない。しかしなが
ら管内の滞水部等は貝類が付着し易い部位であ
り、ポリオレフインといえども貝の付着が無視で
きなくなる。一般的な塗装型の防食被覆であれ
ば、このような特別な個所には防汚塗装を上塗り
し対処することができるが、ポリオレフイン被覆
の場合前述のように塗装による対処に問題を残し
ていた。ポリオレフイン中に防汚剤を含有させる
試みもあるが、防汚剤のポリオレフイン中への溶
解或いは分散が困難であるため、長期の防汚に必
要な多量の防汚剤を含有させられないことから、
未だ完成されるに至つていない。 Taking a seawater intake pipe as an example, coating the inner surface with polyolefin provides a sufficient anticorrosive effect, and usually hardly any shellfish adhere to the pipe. However, water retention areas within pipes are areas where shellfish are likely to adhere, and even with polyolefin, the adhesion of shellfish cannot be ignored. With general paint-type anti-corrosion coatings, special areas like this can be treated by overcoating with antifouling paint, but with polyolefin coatings, as mentioned above, problems remain when dealing with paint. . Some attempts have been made to incorporate an antifouling agent into polyolefin, but it is difficult to dissolve or disperse the antifouling agent into polyolefin, so it is not possible to incorporate the large amount of antifouling agent required for long-term antifouling. ,
It has not yet been completed.
本発明者らは上述したポリオレフイン面への防
汚処置について種々検討した結果、本発明を達成
するに至つた。本発明の要旨とするところは、防
食ポリオレフイン被覆の表面に防汚剤を含有した
エチレン―酢酸ビニル共重合体の薄層を設け、更
にこの上にポリオレフインの薄層を設けたことを
特徴とする防汚性を有するポリオレフイン被覆に
ある。なお、本発明にいう被覆用ポリオレフイン
としてはポリエチレン、ポリプロピレン、ポリブ
テン―1等を例示することができる。これらは単
独で用いても混合して用いてもよく、又防食性能
を損わない範囲の変性を加えたものも対象としう
る。勿論カーボンブラツク、酸化防止剤等の添加
は差支えない。以下に本発明を詳細に説明する。 The present inventors have conducted various studies on antifouling treatments for the above-mentioned polyolefin surfaces, and as a result, have achieved the present invention. The gist of the present invention is that a thin layer of ethylene-vinyl acetate copolymer containing an antifouling agent is provided on the surface of the anticorrosive polyolefin coating, and a thin layer of polyolefin is further provided on this. It has a polyolefin coating that has antifouling properties. Incidentally, examples of the polyolefin for coating according to the present invention include polyethylene, polypropylene, polybutene-1, and the like. These may be used alone or in combination, and may be modified to the extent that the anticorrosion performance is not impaired. Of course, carbon black, antioxidants, etc. may be added. The present invention will be explained in detail below.
まず第1図は本発明被覆の一態様例を模式的に
示す断面図であつて、素地鋼材1の上にポリオレ
フインの層2が設けられ、次いで防汚剤を含有し
たエチレン―酢酸ビニル共重合体(以下EVAと
略称する)の薄層3が設けられ、更にこの上をポ
リオレフインの薄層2′で覆つた態様を示す。 First of all, FIG. 1 is a cross-sectional view schematically showing an embodiment of the coating of the present invention, in which a polyolefin layer 2 is provided on a base steel material 1, and then an ethylene-vinyl acetate copolymer layer containing an antifouling agent is provided. An embodiment is shown in which a thin layer 3 of composite (hereinafter abbreviated as EVA) is provided, which is further covered with a thin layer 2' of polyolefin.
こゝで防汚剤としてはたとえばトリフエニル錫
ハイドロオキサイド、トリブチル錫オキサイド等
の有機錫化合物、亜酸化銅等の銅化合物、チアベ
ンダゾール等の殺菌防黴剤などを挙げることがで
きる。 Examples of antifouling agents include organic tin compounds such as triphenyltin hydroxide and tributyltin oxide, copper compounds such as cuprous oxide, and bactericidal and antifungal agents such as thiabendazole.
次に、EVAは防汚剤を多量に溶解或いは分散
含有させうる基剤となり、且ポリオレフインに容
易に熱融着しうる物質として選定したものであ
る。即ち長期の防汚に必要な多量の防汚剤を
EVA中に含有させ、この防汚剤は最表層のポリ
オレフインを通して徐々に放出されるため、長期
に亘り防汚効果を持続させうる。 Next, EVA was selected as a base material that can dissolve or disperse a large amount of an antifouling agent and that can be easily heat-fused to polyolefin. In other words, a large amount of antifouling agent is required for long-term antifouling.
Since this antifouling agent is contained in EVA and is gradually released through the outermost layer of polyolefin, the antifouling effect can be maintained for a long period of time.
この場合、EVAの種類は特に限定するもので
はないが、酢酸ビニル基10〜30%、メルトインデ
ツクス3〜30のものが適している。又EVAに部
分けん化、カルボン酸付加等の変性を加えたもの
を用いてもよい。EVA中の防汚剤濃度は高い方
が防汚効果が長期に持続するが、10〜60%程度が
実用的である。防汚剤含有EVAの厚さは如何様
にも選択できるが、実用上100〜1000μの範囲が
適する。又これを覆うポリオレフインの厚さは50
〜500μの範囲が実用的である。 In this case, the type of EVA is not particularly limited, but one with 10 to 30% vinyl acetate groups and a melt index of 3 to 30 is suitable. Alternatively, EVA modified by partial saponification, carboxylic acid addition, etc. may be used. The higher the concentration of antifouling agent in EVA, the longer the antifouling effect will last, but approximately 10 to 60% is practical. Although the thickness of the antifouling agent-containing EVA can be selected as desired, a range of 100 to 1000 μm is suitable for practical use. Also, the thickness of the polyolefin covering this is 50
A range of ~500μ is practical.
防食用ポリオレフイン被覆上に防汚剤含有
EVA薄層を、更にこの上にポリオレフインの薄
層を形成させるにはたとえば2段階の溶射或いは
流動浸漬、もしくは防汚剤含有EVAとポリオレ
フインの積層シートの熱融着などの手段を適宜採
用することができる。 Contains antifouling agent on anticorrosive polyolefin coating
In order to form a thin EVA layer and further a thin layer of polyolefin thereon, appropriate methods such as two-step thermal spraying, fluidized dipping, or heat fusion of a laminated sheet of antifouling agent-containing EVA and polyolefin may be employed. I can do it.
本発明のポリオレフイン被覆は下記に挙げるよ
うな利点を有する。 The polyolefin coating of the present invention has the following advantages.
防食用ポリオレフイン、防汚剤含有EVA、
及びポリオレフインの薄層は夫々強固に融着し
ており長期に亘つて剥離の危惧がない。 Anticorrosive polyolefin, EVA containing antifouling agent,
The thin layers of polyolefin and polyolefin are firmly fused to each other, and there is no risk of peeling over a long period of time.
防汚剤含有EVA薄層はポリオレフインを介
して外界と接するため、防汚剤の放出が適度に
抑制され、防汚効果が長期間持続する。 Since the antifouling agent-containing EVA thin layer comes into contact with the outside world through the polyolefin, the release of the antifouling agent is moderately suppressed, and the antifouling effect lasts for a long time.
防汚機能が低下したときには表層部の再処理
による機能更新が容易である。 When the antifouling function deteriorates, it is easy to update the function by reprocessing the surface layer.
防汚処理の施工に有機溶剤を用いないため安
全衛生上有利である。 It is advantageous in terms of safety and health because no organic solvent is used in the antifouling treatment.
次に本発明の効果を実施例にて具体的に説明す
る。 Next, the effects of the present invention will be specifically explained using examples.
実施例
呼び径125mm、4m長の鋼管の外面に押出法に
より、密度0.935、メルトインデツクス0.4のポリ
エチレンを2mmの厚さで被覆したものを2本用意
した(A,Bと呼称を付す)。Example Two steel pipes with a nominal diameter of 125 mm and a length of 4 m were coated with polyethylene having a density of 0.935 and a melt index of 0.4 to a thickness of 2 mm by extrusion on the outer surface (designated as A and B).
Aには上記被覆施工の残熱を有する間に引続い
てトリブチル錫オキサイド30%を含有する酢酸ビ
ニル基19%のEVAを0.3mmの厚さに片面塗布した
上記と同質の0.2mmのポリエチレンテープ(100mm
巾)を重ね層をとらずにらせん巻し本発明被覆を
完成した。冷却後上記テープの下地への接着は極
めて強固であつた。 A is a 0.2 mm polyethylene tape of the same quality as above, which was coated on one side with 19% vinyl acetate EVA containing 30% tributyltin oxide to a thickness of 0.3 mm while still retaining the residual heat from the above coating construction. (100mm
The coating of the present invention was completed by overlapping the layers (width) and spirally winding them without removing any layers. After cooling, the adhesion of the tape to the substrate was extremely strong.
Bはポリエチレン被覆のまゝで比較材とした。 B was used as a comparison material with the polyethylene coating still on.
これらA,B両試験体を2年間海中に浸漬した
結果、Aの本発明被覆には貝類、藻類の付着が皆
無であつたのに対し、比較材Bには若干の緑藻、
セルプラ及び数十個のフジツボの付着が見られ
た。 As a result of immersing both test specimens A and B in the sea for two years, the coating of the present invention in A had no adhesion of shellfish or algae, whereas the comparative material B had some green algae and
Adhesion of celluloid and several dozen barnacles was observed.
なお、Aは残存防汚剤の量から更に2年以上の
防汚寿命が推定されたが、表面に被覆したEVA
―ポリエチレンの被覆を加熱して剥離し、次いで
新規材と同じ構成のEVAとポリエチレンの薄層
を溶射法によつて付与し、新規材と同様の本発明
被覆を更新することができた。 In addition, A was estimated to have an antifouling life of 2 years or more based on the amount of residual antifouling agent, but the EVA coated on the surface
- The polyethylene coating was peeled off by heating, and then a thin layer of EVA and polyethylene with the same composition as the new material was applied by thermal spraying, making it possible to renew the inventive coating similar to the new material.
第1図は本発明被覆の構成を模式的に示す断面
図である。
1…素地鋼材、2,2′…ポリオレフイン、3
…防汚剤を含有したEVA。
FIG. 1 is a sectional view schematically showing the structure of the coating of the present invention. 1...Base steel material, 2,2'...Polyolefin, 3
...EVA containing antifouling agent.
Claims (1)
含有したエチレン―酢酸ビニル共重合体の薄層を
設け、更にこの上にポリオレフインの薄層を設け
たことを特徴とする防汚性を有するポリオレフイ
ン被覆。1. A polyolefin coating with antifouling properties, characterized in that a thin layer of ethylene-vinyl acetate copolymer containing an antifouling agent is provided on the surface of the anticorrosive polyolefin coating, and a thin layer of polyolefin is further provided on top of this. .
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12167483A JPS6015125A (en) | 1983-07-06 | 1983-07-06 | Stainproof polyolefin covering |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP12167483A JPS6015125A (en) | 1983-07-06 | 1983-07-06 | Stainproof polyolefin covering |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6015125A JPS6015125A (en) | 1985-01-25 |
JPS6151986B2 true JPS6151986B2 (en) | 1986-11-11 |
Family
ID=14817076
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP12167483A Granted JPS6015125A (en) | 1983-07-06 | 1983-07-06 | Stainproof polyolefin covering |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6015125A (en) |
-
1983
- 1983-07-06 JP JP12167483A patent/JPS6015125A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS6015125A (en) | 1985-01-25 |
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