JPH04290692A - Coated inner surface steel pipe for resisting sour - Google Patents
Coated inner surface steel pipe for resisting sourInfo
- Publication number
- JPH04290692A JPH04290692A JP3056550A JP5655091A JPH04290692A JP H04290692 A JPH04290692 A JP H04290692A JP 3056550 A JP3056550 A JP 3056550A JP 5655091 A JP5655091 A JP 5655091A JP H04290692 A JPH04290692 A JP H04290692A
- Authority
- JP
- Japan
- Prior art keywords
- steel pipe
- pipe
- weight
- stainless steel
- parts
- 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.)
- Granted
Links
- 229910000831 Steel Inorganic materials 0.000 title claims abstract description 34
- 239000010959 steel Substances 0.000 title claims abstract description 34
- 229910001220 stainless steel Inorganic materials 0.000 claims abstract description 20
- 239000010935 stainless steel Substances 0.000 claims abstract description 19
- 238000000576 coating method Methods 0.000 claims abstract description 14
- 239000011248 coating agent Substances 0.000 claims abstract description 13
- 229910000975 Carbon steel Inorganic materials 0.000 claims abstract description 6
- 239000010962 carbon steel Substances 0.000 claims abstract description 6
- 239000003973 paint Substances 0.000 claims description 23
- 150000001412 amines Chemical class 0.000 claims description 16
- 239000004952 Polyamide Substances 0.000 claims description 15
- 229920002647 polyamide Polymers 0.000 claims description 15
- 239000004593 Epoxy Substances 0.000 claims description 14
- 239000003822 epoxy resin Substances 0.000 claims description 14
- 229920000647 polyepoxide Polymers 0.000 claims description 14
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- -1 aliphatic diamine Chemical class 0.000 claims description 8
- 239000000049 pigment Substances 0.000 claims description 8
- 229930185605 Bisphenol Natural products 0.000 claims description 7
- 239000000945 filler Substances 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 6
- 238000006243 chemical reaction Methods 0.000 claims description 6
- 239000000539 dimer Substances 0.000 claims description 6
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims description 6
- NDKWCCLKSWNDBG-UHFFFAOYSA-N zinc;dioxido(dioxo)chromium Chemical compound [Zn+2].[O-][Cr]([O-])(=O)=O NDKWCCLKSWNDBG-UHFFFAOYSA-N 0.000 claims description 6
- 230000003449 preventive effect Effects 0.000 claims description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 3
- 125000000466 oxiranyl group Chemical group 0.000 claims description 3
- 239000000454 talc Substances 0.000 claims description 3
- 229910052623 talc Inorganic materials 0.000 claims description 3
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 3
- 239000002075 main ingredient Substances 0.000 claims 1
- 238000003466 welding Methods 0.000 abstract description 14
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 abstract description 12
- 229910000037 hydrogen sulfide Inorganic materials 0.000 abstract description 12
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 abstract description 6
- 239000003345 natural gas Substances 0.000 abstract description 3
- 238000005422 blasting Methods 0.000 abstract 1
- 230000008878 coupling Effects 0.000 abstract 1
- 238000010168 coupling process Methods 0.000 abstract 1
- 238000005859 coupling reaction Methods 0.000 abstract 1
- 230000003628 erosive effect Effects 0.000 abstract 1
- 238000005260 corrosion Methods 0.000 description 10
- 230000007797 corrosion Effects 0.000 description 9
- 150000003839 salts Chemical class 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 4
- 238000005304 joining Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 230000007774 longterm Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 239000003981 vehicle Substances 0.000 description 3
- 239000010953 base metal Substances 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000010422 painting Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 229910000859 α-Fe Inorganic materials 0.000 description 2
- XBTRYWRVOBZSGM-UHFFFAOYSA-N (4-methylphenyl)methanediamine Chemical compound CC1=CC=C(C(N)N)C=C1 XBTRYWRVOBZSGM-UHFFFAOYSA-N 0.000 description 1
- FVCSARBUZVPSQF-UHFFFAOYSA-N 5-(2,4-dioxooxolan-3-yl)-7-methyl-3a,4,5,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C(C(OC2=O)=O)C2C(C)=CC1C1C(=O)COC1=O FVCSARBUZVPSQF-UHFFFAOYSA-N 0.000 description 1
- 229920003319 Araldite® Polymers 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 1
- 229910000589 SAE 304 stainless steel Inorganic materials 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229910000963 austenitic stainless steel Inorganic materials 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 229910001039 duplex stainless steel Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000007665 sagging Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は、硫化水素を含む天然ガ
ス、ギャザリングパイプ等の内面塗装鋼管に関するもの
であって、特に硫化水素、塩化合物等の腐食性物質を含
む厳しい環境で使用する内面塗装鋼管に係わるものであ
る。[Industrial Application Field] The present invention relates to natural gas containing hydrogen sulfide, internally coated steel pipes such as gathering pipes, and in particular to internally coated steel pipes used in harsh environments containing corrosive substances such as hydrogen sulfide and salt compounds. This relates to painted steel pipes.
【0002】0002
【従来の技術】天然ガス等の輸送を目的としたパイプラ
インなど、通常地中に埋設して使用されるものは、埋設
されてからは、メンテナンスが行ないにくいこと、ギャ
ザリングパイプ等の硫化水素や高塩分を含む腐食が激し
い環境で使用するものにおいては、パイプの取替え頻度
が多くコストが高いことが理由で、長期耐久性が要求さ
れる。そのため特に管の耐用年数に影響を及ぼす腐食に
対しては、種々の方法で対処している。最も一般的なも
のとして、塗装による被覆が行なわれており、管外面の
みならず内面にも塗装を施すことが要求されている。と
ころが鋼管の溶接継手部にあっては、溶接熱によって塗
膜の損傷を無くすため、予じめ管端を無塗装として溶接
後塗装する手段が取られている。その場合、作業者が管
内に入れる大径サイズの鋼管の場合は、比較的溶接継手
部の塗装作業が容易であるが、作業者が管内に入れない
ような比較的小径サイズの鋼管の場合、溶接継手部の塗
装は、きわめて困難である。小径管内面の溶接継手部の
塗装法として、特公昭48−38460号、特公昭49
−27410号、実公昭51−15829号等があるが
、いずれも溶接継手部の下地処理が完全に出来ないため
、非溶接部に比べて耐食性が極端に劣り、長期の耐久性
が望めない。また、鋼管の内面塗装として、従来主とし
てタールエポキシ、ピュアーエポキシなどの塗料の塗装
が行なわれてきた。しかし、これらの塗料は、硫化水素
、高塩分を含む厳しい腐食環境においては耐食性が十分
でなく、また、ステンレス鋼の継手にした場合、ステン
レス鋼との密着性も炭素鋼に比べて劣るため、継手部の
防食が確保できない。[Prior Art] Pipelines that are normally buried underground, such as pipelines for the purpose of transporting natural gas, etc., are difficult to maintain once they are buried, and hydrogen sulfide, such as gathering pipes, etc. For products used in highly corrosive environments containing high salt content, long-term durability is required because pipes must be replaced frequently and are expensive. Therefore, various methods are used to deal with corrosion, which particularly affects the service life of pipes. The most common method is coating, and it is required to coat not only the outer surface of the pipe but also the inner surface. However, in the case of welded joints of steel pipes, in order to prevent damage to the coating film due to welding heat, the pipe ends are left unpainted in advance and painted after welding. In this case, it is relatively easy to paint the welded joints of large-diameter steel pipes that workers can fit inside the pipe, but for relatively small-diameter steel pipes that workers cannot fit into the pipes, Painting welded joints is extremely difficult. As a coating method for welded joints on the inner surface of small diameter pipes, Japanese Patent Publication No. 48-38460 and Japanese Patent Publication No. 49
-27410, Utility Model Publication No. 51-15829, etc., but in both cases, the groundwork of the welded joint cannot be completely prepared, so the corrosion resistance is extremely inferior to that of the non-welded part, and long-term durability cannot be expected. In addition, conventionally, the inner surface of steel pipes has been mainly coated with paints such as tar epoxy and pure epoxy. However, these paints do not have sufficient corrosion resistance in severe corrosive environments containing hydrogen sulfide and high salt content, and when applied to stainless steel joints, their adhesion to stainless steel is inferior to that of carbon steel. Corrosion protection of the joint cannot be ensured.
【0003】0003
【発明が解決しようとする課題】本発明の目的は、硫化
水素や高塩分に対して不活性、且つステンレスとの密着
性が優れた塗料とステンレス継手によって、特にステン
レスとの塗膜密着性を改善することで、耐久性の優れた
内面塗装鋼管を提供することにある。[Problems to be Solved by the Invention] The object of the present invention is to improve the adhesion of the paint film to stainless steel in particular by using a paint and stainless steel joint that is inert to hydrogen sulfide and high salt and has excellent adhesion to stainless steel. The objective is to provide inner-coated steel pipes with excellent durability.
【0004】0004
【課題を解決するための手段】すなわち、本発明は炭素
鋼管の両端部にステンレス管を溶接接合し、該鋼管内面
をブラスト処理した後、溶接接合部を含むステンレスの
一部まで内面塗装した鋼管を溶接接合する耐サワー用内
面塗装鋼管において、内面塗装に用いる塗料が、一分子
当たり1〜2個のオキシラン環を有するエポキシ当量4
00〜2500のビスフェノール型エポキシ樹脂を主剤
とし、脂肪族ジアミンとダイマー酸から成るポリアミド
アミン2〜4モルに対してエポキシ当量180〜140
0のビスフェノール型エポキシ樹脂1モルを反応して成
るポリアミドアミンアダクトを硬化剤として、エポキシ
樹脂とポリアミドアミンアダクトの比が反応当量で0.
8/1〜1.4/1のベヒクル100重量部に対して酸
化チタン及びタルクの充填剤を合計50〜200重量部
ならびに防錆顔料としてジンククロメートZTO型を3
〜40重量部を主剤及び/または硬化剤中に含むことを
特徴とする耐サワー内面塗装鋼管であり、これによって
硫化水素、高塩分等を含む腐食環境において、長期耐久
性を可能とするものである。[Means for Solving the Problems] That is, the present invention provides a steel pipe in which a stainless steel pipe is welded to both ends of a carbon steel pipe, the inner surface of the steel pipe is blasted, and then the inner surface of a portion of the stainless steel including the welded joint is painted. In sour-resistant internally coated steel pipes that are welded together, the paint used for the internal coating has an epoxy equivalent of 4 and has 1 to 2 oxirane rings per molecule.
00 to 2500 bisphenol type epoxy resin as the main resin, and the epoxy equivalent is 180 to 140 with respect to 2 to 4 moles of polyamide amine consisting of aliphatic diamine and dimer acid.
Using a polyamide amine adduct obtained by reacting 1 mole of a bisphenol type epoxy resin of 0.0 as a curing agent, the ratio of the epoxy resin to the polyamide amine adduct is 0.0 in terms of reaction equivalent.
A total of 50 to 200 parts by weight of fillers of titanium oxide and talc and 3 parts of zinc chromate ZTO type as a rust preventive pigment were added to 100 parts by weight of vehicle of 8/1 to 1.4/1.
This is a sour-resistant inner-coated steel pipe characterized by containing ~40 parts by weight of the main agent and/or hardening agent, which enables long-term durability in corrosive environments containing hydrogen sulfide, high salt content, etc. be.
【0005】以下本発明を詳細に説明する。本発明の炭
素鋼管の両端部に使用するステンレス管は、例えば、J
IS G−3459のSUS304、SUS316の
オーステナイト系ステンレス鋼、JIS G−430
3〜4307規格のSUS329J1、ASTM A
240規格の329、DIN1.4462規格のX8C
rNiMo275、GOST5632規格のOX21H
5T、新日本製鐵規格のYUS−DX1、YUS−31
7LN等の二相ステンレス鋼があるが、その中でもステ
ンレス鋼中のCr当量が22〜24%、Ni当量が6〜
7%、フェライト量が40〜60%のフェライト量を含
む二相ステンレス鋼が良い。溶接接合は、例えばYUS
−DX1の場合、サブマージアーク溶接、被覆アーク溶
接、およびTIG溶接には共金系溶接材料を使用する。
また、本発明において使用する塗料は、ベヒクルとして
、一分子当たり1〜2個のオキシラン環を有するビスフ
ェノールAとエピハロヒドリンとの付加反応によって得
られるエポキシ当量が400〜1400のエポキシ樹脂
、及び脂肪族ジアミンとダイマー酸から成るポリアミド
アミンとビスフェノール型エポキシ樹脂を2/1〜4/
1の反応モル比で反応させて得られる化合物(いわゆる
ポリアミドアミンアダクト)とから成る。この樹脂は、
ビスフェノールAのジグリシジルエーテルと呼ばれてい
るものである。具体的には、エピコート(油化シェルエ
ポキシ(株))、エポトート(東都化成(株))、アラ
ルダイト(チバガイギー)、エピクロン(大日本インキ
化学工業(株))等の銘柄で市販されているもので、エ
ポキシ当量が400〜2500、分子量が800〜30
00のエポキシ樹脂の使用が適当である。エポキシ当量
が400以下になると反応性が高くなり、ポットライフ
が短くなって作業性が悪くなる。またこの場合、硬化物
が脆くなってAPI規格の曲げ試験に合格しない。また
、エポキシ当量が2500を超えると、常温に於ける反
応が非常に遅くなるとともに、粘度が高くなり過ぎて塗
装が困難である。一方の硬化剤となるポリアミドアミン
は、脂肪族ジアミンとダイマー酸から得られるポリアミ
ドアミンの2〜4モルとエポキシ当量180〜1400
のビスフェノール型エポキシ樹脂1モルを反応して得ら
れる。
このポリアミドアミンアダクトの1成分であるダイマー
酸は、天然油脂中の不飽和脂肪酸を加熱重合して得るこ
とが出来る。具体的には、バーサダイム(ヘンケル日本
(株))が挙げられる。ポリアミドアミンアダクトの二
つ目の成分である脂肪族ジアミンとしては、キシレンジ
アミン、エチレンジアミン、ヘキサメチレンジアミン、
ビスアミノプロピル−テトラオキサスピロウンデカンな
どが使用できる。ポリアミドアミンアダクトの三つ目の
成分であるビスフェノール型エポキシ樹脂は、エポキシ
当量180〜1400、好ましくは、180〜500で
ある必要がある。エポキシ樹脂のエポキシ当量が140
0を超えるとアダクト反応が難しくなる。また、エポキ
シ当量が180未満では、一分子当たりのエポキシ基が
少なくなり、望みの塗膜の硬さや柔軟性が得られない。
本発明における塗料のベヒクル成分のひとつであるポリ
アミドアミンアダクトの原料であるダイマー酸は、一般
的なエポキシ樹脂アミン硬化物の硬くて脆いという性質
を打ち破り、特にもう一つの原料である脂肪族ジアミン
との反応でもって、硬くて柔軟性のあるいわゆる弾性体
のごとき性質の硬化樹脂を与える作用をする。このエポ
キシ樹脂とポリアミドアミンアダクトの配合比は、当量
比で0.8/1〜1.4/1、好ましくは、0.8/1
〜1.2/1である。この比が、0.8/1未満では、
塗膜が軟らかくなり過ぎるし、耐水性などの防食性能も
悪くなる。一方、配合比が1.4/1を超えると塗膜が
逆に硬くて脆くなり、かつ、耐水性などの防食性能も悪
くなる。次に本発明に於ける塗料の充填剤及び防錆顔料
としては、硫化水素に対して不活性で、水可溶分が小さ
いものの中から選択することで硫化水素に対して安定な
塗膜とした。即ち、充填剤としては、酸化チタン、タル
ク、防錆顔料としては、ジンククロメートZTO型を耐
塩水噴霧性、耐水性、耐塩水性、及び硫化水素飽和水浸
漬試験を行ない選定した。The present invention will be explained in detail below. The stainless steel pipe used at both ends of the carbon steel pipe of the present invention is, for example, J
IS G-3459 SUS304, SUS316 austenitic stainless steel, JIS G-430
3-4307 standard SUS329J1, ASTM A
329 of 240 standard, X8C of DIN1.4462 standard
rNiMo275, OX21H of GOST5632 standard
5T, Nippon Steel standard YUS-DX1, YUS-31
There are duplex stainless steels such as 7LN, but among them, the Cr equivalent in the stainless steel is 22 to 24% and the Ni equivalent is 6 to 6%.
Duplex stainless steel containing a ferrite content of 7% and a ferrite content of 40 to 60% is preferred. For example, YUS
- In the case of DX1, a matching welding material is used for submerged arc welding, shielded arc welding, and TIG welding. In addition, the paint used in the present invention includes, as a vehicle, an epoxy resin having an epoxy equivalent of 400 to 1400 obtained by the addition reaction of bisphenol A having 1 to 2 oxirane rings per molecule and epihalohydrin, and an aliphatic diamine. and polyamide amine consisting of dimer acid and bisphenol type epoxy resin from 2/1 to 4/
It consists of a compound obtained by reacting at a reaction molar ratio of 1 (so-called polyamide amine adduct). This resin is
It is called diglycidyl ether of bisphenol A. Specifically, those commercially available under brands such as Epicote (Yuka Shell Epoxy Co., Ltd.), Epotote (Toto Kasei Co., Ltd.), Araldite (Ciba Geigy), and Epiclon (Dainippon Ink & Chemicals Co., Ltd.). and the epoxy equivalent is 400-2500 and the molecular weight is 800-30.
00 epoxy resin is suitable. When the epoxy equivalent is less than 400, the reactivity becomes high, the pot life becomes short, and the workability deteriorates. Moreover, in this case, the cured product becomes brittle and does not pass the API standard bending test. Furthermore, if the epoxy equivalent exceeds 2500, the reaction at room temperature becomes extremely slow and the viscosity becomes too high, making coating difficult. The polyamide amine used as one of the curing agents contains 2 to 4 moles of polyamide amine obtained from an aliphatic diamine and a dimer acid, and an epoxy equivalent of 180 to 1,400.
It is obtained by reacting 1 mole of bisphenol type epoxy resin. Dimer acid, which is one component of this polyamide amine adduct, can be obtained by heating and polymerizing unsaturated fatty acids in natural oils and fats. A specific example is Versadime (Henkel Japan Ltd.). Aliphatic diamines, which are the second component of polyamide amine adduct, include xylene diamine, ethylene diamine, hexamethylene diamine,
Bisaminopropyl-tetraoxaspiroundecane and the like can be used. The bisphenol type epoxy resin which is the third component of the polyamide amine adduct needs to have an epoxy equivalent of 180 to 1400, preferably 180 to 500. The epoxy equivalent of the epoxy resin is 140
If it exceeds 0, adduct reaction becomes difficult. Furthermore, if the epoxy equivalent is less than 180, the number of epoxy groups per molecule will decrease, making it impossible to obtain the desired hardness and flexibility of the coating film. Dimer acid, which is a raw material for polyamide amine adduct, which is one of the vehicle components of the paint in the present invention, overcomes the hard and brittle properties of general epoxy resin amine cured products, and is particularly effective when used with aliphatic diamine, another raw material. This reaction provides a cured resin with properties similar to that of an elastic body, which is hard and flexible. The blending ratio of this epoxy resin and polyamide amine adduct is 0.8/1 to 1.4/1 in terms of equivalent ratio, preferably 0.8/1.
~1.2/1. If this ratio is less than 0.8/1,
The paint film will become too soft and its anti-corrosion properties such as water resistance will deteriorate. On the other hand, if the blending ratio exceeds 1.4/1, the coating film will become hard and brittle, and the anticorrosion performance such as water resistance will also deteriorate. Next, fillers and anti-rust pigments for the paint in the present invention are selected from those that are inert to hydrogen sulfide and have a small water-soluble content, thereby creating a coating film that is stable against hydrogen sulfide. did. That is, titanium oxide and talc were selected as the filler, and zinc chromate ZTO type was selected as the anticorrosive pigment after conducting salt spray resistance, water resistance, salt water resistance, and hydrogen sulfide saturated water immersion tests.
【0006】これらの配合量は、重量基準でバインダー
成分100重量部に対して充填剤が50〜200重量部
、防錆顔料が3〜40重量部である。充填剤の量が50
重量部未満では、塗膜強度が低くて衝撃、曲げ性などが
悪くなる。また、充填剤の量が200重量部を超える場
合は、バインダーが不足して均一な塗膜が形成されず、
ピンホールなどの欠陥を生じたり、物性が低下するので
好ましくない。次に、防錆顔料が3重量部未満であると
防食性能が不十分であり、40重量部を超えると水可溶
分を押えた顔料を用いても水に溶解する防錆顔料の絶対
量が多くなって、逆に防食性能が悪くなるので好ましく
ない。本発明に於ける塗料は、これまで述べた必須成分
の他に、適当なハジキ防止剤、ダレ止め剤、流展剤など
の添加剤類を含有することが出来る。また、塗装作業性
を改良するために、溶剤類も必要に応じて配合すること
が出来る。以下、実施例に従って本発明を更に詳しく説
明する。[0006] The blending amounts of these materials are, on a weight basis, 50 to 200 parts by weight of the filler and 3 to 40 parts by weight of the rust preventive pigment to 100 parts by weight of the binder component. The amount of filler is 50
If the amount is less than 1 part by weight, the strength of the coating film will be low, resulting in poor impact and bending properties. Additionally, if the amount of filler exceeds 200 parts by weight, the binder will be insufficient and a uniform coating will not be formed.
This is not preferable because it causes defects such as pinholes and deteriorates physical properties. Next, if the amount of the rust preventive pigment is less than 3 parts by weight, the anticorrosive performance will be insufficient, and if it exceeds 40 parts by weight, the absolute amount of the rust preventive pigment will dissolve in water even if a pigment with a reduced water-soluble content is used. This is undesirable because it increases the amount of corrosion and deteriorates the anticorrosion performance. In addition to the above-mentioned essential components, the paint according to the present invention can contain appropriate additives such as anti-cissing agents, anti-sagging agents, and spreading agents. Further, in order to improve painting workability, solvents can be added as necessary. Hereinafter, the present invention will be explained in more detail according to Examples.
【0007】[0007]
【実施例】(実施例及び比較例)■ 供試鋼管は、8
00mm長のSGP鋼管(200A)の両端に100m
m長のYUS−317LN鋼管を溶接後、アルミナグリ
ットでブラスト処理を行ない、管端より50mm付近ま
で、第1表に示す組成の塗料を乾燥膜厚200〜250
μm塗装し、100℃×90分の乾燥をした。更に、前
記の塗装鋼管2本をTIG溶接にて接合した後、両端に
ステンレスフランジを取付け、既設のギャザリングパイ
プに取付け、第2表の腐食環境のもとで2年間暴露試験
を行なった。
■ 供試鋼管は、800mm長のSGP鋼管(200
A)の両端に100mm長のSUS−304鋼管を溶接
後、アルミナグリットでブラスト処理を行ない、管端よ
り50mm付近まで、第1表に示す組成の塗料を乾燥膜
厚200〜250μm塗装し、100℃×90分の乾燥
をした。更に、前記の塗装鋼管2本をTIG溶接にて接
合した後、両端にステンレスフランジを取付け、既設の
ギャザリングパイプに取付け、第2表の腐食環境のもと
で2年間暴露試験を行なった。[Example] (Example and Comparative Example) ■ The test steel pipe is 8
100m on both ends of 00mm long SGP steel pipe (200A)
After welding a m-long YUS-317LN steel pipe, it is blasted with alumina grit, and a paint with the composition shown in Table 1 is applied to the area up to about 50 mm from the end of the pipe to a dry film thickness of 200 to 250 mm.
It was coated with μm coating and dried at 100°C for 90 minutes. Furthermore, after joining the two painted steel pipes by TIG welding, stainless steel flanges were attached to both ends, and the pipes were attached to an existing gathering pipe, and an exposure test was conducted for two years under the corrosive environment shown in Table 2. ■ The test steel pipe is an 800mm long SGP steel pipe (200mm long).
After welding a 100 mm long SUS-304 steel pipe to both ends of A), it was blasted with alumina grit, and a paint with the composition shown in Table 1 was applied to about 50 mm from the pipe end to a dry film thickness of 200 to 250 μm. It was dried for 90 minutes at ℃. Furthermore, after joining the two painted steel pipes by TIG welding, stainless steel flanges were attached to both ends, and the pipes were attached to an existing gathering pipe, and an exposure test was conducted for two years under the corrosive environment shown in Table 2.
【0008】■ 供試鋼管は、800mm長のSGP
鋼管(200A)の両端に100mm長のSUS−31
6鋼管を溶接後、アルミナグリットでブラスト処理を行
ない、管端より50mm付近まで、第1表に示す組成の
塗料を乾燥膜厚200〜250μm塗装し、100℃×
90分の乾燥をした。更に、前記の塗装鋼管2本をTI
G溶接にて接合した後、両端にステンレスフランジを取
付け、既設のギャザリングパイプに取付け、第2表の腐
食環境のもとで2年間暴露試験を行なった。[0008] ■ The test steel pipe is SGP with a length of 800 mm.
100mm long SUS-31 on both ends of steel pipe (200A)
6 After welding the steel pipes, they were blasted with alumina grit, and a paint with the composition shown in Table 1 was applied to a dry film thickness of 200 to 250 μm from the pipe end to about 50 mm, and heated at 100°C.
It was dried for 90 minutes. Furthermore, the two painted steel pipes mentioned above were treated with TI.
After joining by G welding, stainless steel flanges were attached to both ends, attached to an existing gathering pipe, and an exposure test was conducted for 2 years under the corrosive environment shown in Table 2.
【0009】■ 供試鋼管は、1000mm長のSG
P鋼管(200A)にアルミナグリットでブラスト処理
を行ない、管端より50mm付近まで、第1表に示す組
成の塗料を乾燥膜厚200〜250μm塗装し、100
℃×90分の乾燥をした。更に、前記の塗装鋼管2本を
TIG溶接にて接合した後、両端に炭素鋼のフランジを
取付け、既設のギャザリングパイプに取付け、第2表の
腐食環境のもとで2年間暴露試験を行なった。[0009]■ The test steel pipe is SG with a length of 1000 mm.
A P steel pipe (200A) was blasted with alumina grit, and a paint with the composition shown in Table 1 was applied to a dry film thickness of 200 to 250 μm from the end of the pipe to about 50 mm.
It was dried for 90 minutes at ℃. Furthermore, after joining the above two painted steel pipes by TIG welding, carbon steel flanges were attached to both ends, attached to an existing gathering pipe, and an exposure test was conducted for two years under the corrosive environment shown in Table 2. .
【0010】0010
【表1】[Table 1]
【0011】[0011]
【表2】[Table 2]
【0012】0012
【表3】[Table 3]
【0013】2年間暴露後、継手部及び母材部を切りだ
し、ステンレス部の塗膜密着力、孔食、応力腐食割れの
評価、及び母材部の塗膜外観、ピンホール、塗膜密着力
、絶縁抵抗の評価を行なった。結果を第3表に示す。After 2 years of exposure, the joint and base metal parts were cut out, and the paint film adhesion, pitting corrosion, and stress corrosion cracking on the stainless steel parts were evaluated, and the appearance of the paint film on the base metal parts, pinholes, and paint film adhesion were evaluated. The strength and insulation resistance were evaluated. The results are shown in Table 3.
【0014】[0014]
【表4】[Table 4]
【0015】[0015]
【表5】[Table 5]
【0016】[0016]
【発明の効果】本発明によれば、継手部のステンレスの
孔食、応力腐食割れは全く見られず、ステンレスと塗膜
との密着も剥離状態が塗膜の凝集破壊であり、良好であ
った。また母材部では、塗膜の変色、ピンホールはなく
、塗膜密着力及び絶縁抵抗共に初期の品質を確保してお
り、硫化水素、高塩分等の厳しい腐食環境に対して優れ
た耐久性を発揮する。[Effects of the Invention] According to the present invention, there is no pitting corrosion or stress corrosion cracking of the stainless steel in the joint, and the adhesion between the stainless steel and the paint film is good because the peeling state is due to cohesive failure of the paint film. Ta. In addition, there is no discoloration or pinholes in the paint film on the base material, and the initial quality of both paint film adhesion and insulation resistance is maintained, and it has excellent durability against harsh corrosive environments such as hydrogen sulfide and high salt content. demonstrate.
Claims (1)
接接合し、該鋼管内面をブラスト処理した後、溶接接合
部を含むステンレスの一部まで内面塗装した鋼管を溶接
接合する耐サワー用内面塗装鋼管において、内面塗料に
用いる塗料が、一分子当たり1〜2個のオキシラン環を
有するエポキシ当量400〜2500のビスフェノール
型エポキシ樹脂を主剤とし、脂肪族ジアミンとダイマー
酸から成るポリアミドアミン2〜4モルに対してエポキ
シ当量180〜1400のビスフェノール型エポキシ樹
脂1モルを反応して成るポリアミドアミンアダクトを硬
化剤として、エポキシ樹脂とポリアミドアミンアダクト
の比が反応当量で0.8/1〜1.4/1のベヒクル1
00重量部に対して酸化チタン及びタルクの充填剤を合
計50〜200重量部ならびに防錆顔料としてジンクク
ロメートZTO型を3〜40重量部を主剤及び/または
硬化剤中に含むことを特徴とする耐サワー用内面塗装鋼
管。Claim 1: A sour-resistant inner surface coating in which a stainless steel pipe is welded to both ends of a carbon steel pipe, the inner surface of the steel pipe is blasted, and then a part of the stainless steel including the welded joint is welded and joined. In steel pipes, the paint used for the internal surface coating is based on a bisphenol type epoxy resin having 1 to 2 oxirane rings per molecule and having an epoxy equivalent of 400 to 2,500, and contains 2 to 4 moles of polyamide amine consisting of an aliphatic diamine and a dimer acid. Using a polyamide amine adduct obtained by reacting 1 mol of bisphenol type epoxy resin with an epoxy equivalent of 180 to 1400 as a curing agent, the ratio of the epoxy resin to the polyamide amine adduct is 0.8/1 to 1.4/ in terms of reaction equivalent. 1 vehicle 1
00 parts by weight, a total of 50 to 200 parts by weight of titanium oxide and talc fillers and 3 to 40 parts by weight of zinc chromate ZTO type as a rust preventive pigment are contained in the main ingredient and/or curing agent. Internally coated steel pipe for sour resistance.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3056550A JPH0784914B2 (en) | 1991-03-20 | 1991-03-20 | Inner coated steel pipe for sour resistance |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP3056550A JPH0784914B2 (en) | 1991-03-20 | 1991-03-20 | Inner coated steel pipe for sour resistance |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH04290692A true JPH04290692A (en) | 1992-10-15 |
JPH0784914B2 JPH0784914B2 (en) | 1995-09-13 |
Family
ID=13030211
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP3056550A Expired - Lifetime JPH0784914B2 (en) | 1991-03-20 | 1991-03-20 | Inner coated steel pipe for sour resistance |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0784914B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003532778A (en) * | 2000-05-06 | 2003-11-05 | ヘンケル・コマンディットゲゼルシャフト・アウフ・アクチエン | Conductive organic paint |
JP2007527926A (en) * | 2003-12-29 | 2007-10-04 | カウンシル オブ サイエンティフィク アンド インダストリアル リサーチ | Inexpensive, alternative oxygen barrier material for the packaging industry |
JP2013044423A (en) * | 2011-08-26 | 2013-03-04 | Taku Seisakusho:Kk | Piping |
-
1991
- 1991-03-20 JP JP3056550A patent/JPH0784914B2/en not_active Expired - Lifetime
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003532778A (en) * | 2000-05-06 | 2003-11-05 | ヘンケル・コマンディットゲゼルシャフト・アウフ・アクチエン | Conductive organic paint |
JP2007527926A (en) * | 2003-12-29 | 2007-10-04 | カウンシル オブ サイエンティフィク アンド インダストリアル リサーチ | Inexpensive, alternative oxygen barrier material for the packaging industry |
JP4726626B2 (en) * | 2003-12-29 | 2011-07-20 | カウンシル オブ サイエンティフィク アンド インダストリアル リサーチ | Inexpensive, alternative oxygen barrier material for the packaging industry |
JP2013044423A (en) * | 2011-08-26 | 2013-03-04 | Taku Seisakusho:Kk | Piping |
Also Published As
Publication number | Publication date |
---|---|
JPH0784914B2 (en) | 1995-09-13 |
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