JP2999059B2 - Surface treatment method for polyethylene powder lining - Google Patents
Surface treatment method for polyethylene powder liningInfo
- Publication number
- JP2999059B2 JP2999059B2 JP10763892A JP10763892A JP2999059B2 JP 2999059 B2 JP2999059 B2 JP 2999059B2 JP 10763892 A JP10763892 A JP 10763892A JP 10763892 A JP10763892 A JP 10763892A JP 2999059 B2 JP2999059 B2 JP 2999059B2
- Authority
- JP
- Japan
- Prior art keywords
- lining
- polyethylene powder
- polyethylene
- coating
- powder
- 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 - Fee Related
Links
- 239000004698 Polyethylene Substances 0.000 title claims description 37
- -1 polyethylene Polymers 0.000 title claims description 37
- 229920000573 polyethylene Polymers 0.000 title claims description 37
- 239000000843 powder Substances 0.000 title claims description 29
- 238000000034 method Methods 0.000 title claims description 15
- 238000004381 surface treatment Methods 0.000 title 1
- 239000000463 material Substances 0.000 claims description 25
- 238000005422 blasting Methods 0.000 claims description 7
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 claims description 7
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 claims description 7
- 229910000975 Carbon steel Inorganic materials 0.000 claims description 6
- 239000007864 aqueous solution Substances 0.000 claims description 6
- 239000010962 carbon steel Substances 0.000 claims description 6
- 238000002844 melting Methods 0.000 claims description 3
- 230000008018 melting Effects 0.000 claims description 3
- 238000005554 pickling Methods 0.000 claims description 3
- 238000001035 drying Methods 0.000 claims description 2
- 238000011282 treatment Methods 0.000 description 15
- 239000011248 coating agent Substances 0.000 description 13
- 238000000576 coating method Methods 0.000 description 13
- 238000005260 corrosion Methods 0.000 description 10
- 230000007797 corrosion Effects 0.000 description 10
- 230000000694 effects Effects 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 7
- 239000011347 resin Substances 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 229910019142 PO4 Inorganic materials 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 4
- 239000010452 phosphate Substances 0.000 description 4
- 239000005060 rubber Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000011701 zinc Substances 0.000 description 4
- 239000013078 crystal Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000012925 reference material Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 3
- 229910000165 zinc phosphate Inorganic materials 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 238000007739 conversion coating Methods 0.000 description 2
- 238000005536 corrosion prevention Methods 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 238000005238 degreasing Methods 0.000 description 2
- 230000018044 dehydration Effects 0.000 description 2
- 238000006297 dehydration reaction Methods 0.000 description 2
- 239000011572 manganese Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 229910052718 tin Inorganic materials 0.000 description 2
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000010953 base metal Substances 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- CPSYWNLKRDURMG-UHFFFAOYSA-L hydron;manganese(2+);phosphate Chemical compound [Mn+2].OP([O-])([O-])=O CPSYWNLKRDURMG-UHFFFAOYSA-L 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000006864 oxidative decomposition reaction Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000013535 sea water Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- POWFTOSLLWLEBN-UHFFFAOYSA-N tetrasodium;silicate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-][Si]([O-])([O-])[O-] POWFTOSLLWLEBN-UHFFFAOYSA-N 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
- Chemical Treatment Of Metals (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は炭素鋼からなる各種装置
の配管、機器に用いられるポリエチレンライニングの下
地処理方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for treating a surface of a polyethylene lining used for piping and equipment of various devices made of carbon steel.
【0002】[0002]
【従来の技術】従来、ポリエチレン粉体ライニングは炭
素鋼からなる被ライニング材表面を脱脂洗浄し、ブラス
ト処理または酸洗浄してからリン酸塩による化成処理被
膜を形成させたのち、200〜300℃に該被ライニン
グ材を予備加熱して、ポリエチレンの粉体を供給して被
ライニング材の保有熱または被ライニング面の逆側から
の供給熱によりポリエチレンの粉体を熱溶融して連続し
たポリエチレンライニング被膜を形成する方法が行われ
ている。2. Description of the Related Art Conventionally, a polyethylene powder lining is prepared by subjecting the surface of a lining material made of carbon steel to degreasing and washing, blasting or acid washing, and then forming a chemical conversion treatment coating with phosphate, followed by 200 to 300 ° C. The lining material is preheated to supply polyethylene powder, and the polyethylene powder is heated and melted by the retained heat of the lining material or the heat supplied from the opposite side of the lining surface to continuously polyethylene lining A method of forming a coating has been performed.
【0003】[0003]
【発明が解決しようとする課題】これまで、ポリエチレ
ン粉体ライニングは水道用配管あるいは海水取水管など
比較的温度の低い(30℃以下)液と接する環境に多用
され、耐久性の面でもそれなりの実績を有している。と
ころが従来の方法で施工したポリエチレン粉体ライニン
グ材を化学プラント、発電プラントなど液温が50〜6
0℃の環境に用いた場合、ポリエチレンの被膜が短時間
で剥離したり、ブリスタを生じる事故が多発している。
剥離及びブリスタ部の被ライニング面を調査すると、必
ず被ライニング面の腐食が認められることから、従来の
ポリエチレンライニング材は液温が高く、かつ、水蒸気
及び酸素の透過が加速される温度勾配環境に用いた場
合、下地面が腐食されやすいことが分かる。Hitherto, polyethylene powder lining has been frequently used in an environment where it is in contact with a liquid having a relatively low temperature (30 ° C. or less) such as a water supply pipe or a seawater intake pipe, and has a reasonable durability. Has a track record. However, when the polyethylene powder lining material constructed by the conventional method is used in a chemical plant, a power plant, or the like, the liquid temperature is 50-6.
When used in an environment of 0 ° C., there are many accidents in which a polyethylene coating peels off in a short time or blisters occur.
When inspecting the lining surface of the peeling and blister parts, corrosion of the lining surface is always observed.Therefore, the conventional polyethylene lining material has a high liquid temperature and is exposed to a temperature gradient environment where the permeation of water vapor and oxygen is accelerated. It can be seen that when used, the underlying surface is easily corroded.
【0004】従来のポリエチレン粉体ライニング法にお
けるブラスト処理またはリン酸塩による化成処理などの
下地処理は塗装及び樹脂またはゴムライニングなどの下
地処理として産業界で広範囲に適用されている方法であ
るが、200〜300℃で被ライニング材を加熱し、ポ
リエチレン粉末を熱溶融させるポリエチレン粉体ライニ
ング法における下地処理方法としては次のような理由で
必ずしも適正とは言い難い。Undercoating treatments such as blast treatment or chemical conversion treatment with phosphate in the conventional polyethylene powder lining method are widely applied in the industry as undercoating treatments such as coating and resin or rubber lining. It is not always appropriate for the ground treatment method in the polyethylene powder lining method in which the lining material is heated at 200 to 300 ° C. and the polyethylene powder is thermally melted for the following reasons.
【0005】先ず、ブラスト処理は被ライニング面の錆
または異物などを除去することと、ブラストにより生じ
た表面の凹凸のアンカ効果によって、塗膜またはライニ
ングの付着力を向上するとともに、前記錆または異物付
着に起因する局部電池形成による腐食を抑制する狙いが
ある。しかし、ブラスト処理面は活性金属面が露出して
おり、腐食環境に暴露された場合、全面腐食が進行し、
腐食を抑制する効果は期待できない。[0005] First, the blasting treatment removes rust or foreign matter on the surface to be lined and improves the adhesion of the coating film or lining by the anchor effect of the unevenness of the surface caused by the blasting. The aim is to suppress corrosion due to local cell formation due to adhesion. However, the active metal surface is exposed on the blasted surface, and when exposed to a corrosive environment, overall corrosion progresses,
The effect of suppressing corrosion cannot be expected.
【0006】そこで一般の塗装、樹脂ライニング、ゴム
ライニングなどではZn,Sn,Alなどの粉体を配合
したプライマーを塗布し、ブラスト面の腐食を防止する
方法が採用されている。ところが、ポリエチレン粉体ラ
イニングの場合、200〜300℃に加熱するため、前
記防食効果を期待したプライマーは樹脂の熱分解及び前
記Zn,Sn,Alが酸化されて、ZnO2 ,Sn
O2 ,Al2 O3 などに変化し、電気化学的な防食作用
も消失するため使用できず、ライニング用のポリエチレ
ン粉体を直接供給してライニングしている。また、被ラ
イニング材の予備加熱工程及びポリエチレン粉体の溶融
は空気中で行われており、この間に被ライニング材のブ
ラスト面は局部的に酸化され、腐食環境に暴露された場
合、局部電池形成による腐食されやすいFe2 O3 系の
酸化膜が部分的に形成されやすい。Therefore, in general coating, resin lining, rubber lining and the like, a method is adopted in which a primer containing a powder of Zn, Sn, Al or the like is applied to prevent corrosion of the blast surface. However, in the case of polyethylene powder lining, since the primer is heated to 200 to 300 ° C., the primer expected to have the anticorrosion effect is thermally decomposed of the resin and the Zn, Sn, and Al are oxidized, and ZnO 2 , Sn
It changes to O 2 , Al 2 O 3, etc. and cannot be used because the electrochemical anticorrosion action is also lost, and lining is directly supplied by supplying polyethylene powder for lining. In addition, the pre-heating step of the lining material and the melting of the polyethylene powder are performed in the air. During this time, the blast surface of the lining material is locally oxidized, and when exposed to a corrosive environment, a local battery is formed. An Fe 2 O 3 -based oxide film, which is easily corroded by the above, is likely to be partially formed.
【0007】一方、リン酸塩による化成処理被膜を形成
させる下地処理は腐食性物質の拡散抑制及びその被膜中
に含まれる金属塩による電気化学的防錆効果を狙いとし
て一般的に塗装下地処理として適用されている方法であ
る。しかしながら、リン酸塩による化成処理被膜はMn
3 (PO4 )2 ・2MnHPO4 ・4H2 OとFeHP
O4 ・4H2 Oの混合結晶あるいはZn3 (PO4 )2
・4H2 OとFeHPO4 ・2〜4H2 Oの混合結晶あ
るいはγ・Fe2 O3 ・FePO4 ・2H2 OまたはF
eHPO4 ・4〜8H2 Oなどからなっている。これら
の結晶は100〜240℃で結晶水を放出するととも
に、リン酸マンガン系被膜では250℃付近、リン酸亜
鉛系では130℃から酸化分解が始まる。従って、20
0〜300℃で加熱溶融させるポリエチレン粉体ライニ
ングにおいては脱水によるポーラス化、脱水時のリン酸
被膜のクラック発生及び化成処理被膜の付着力の低下ば
かりでなく、リン酸被膜中のMn,Znなどの酸化によ
る防食効果の低下、更にはこれらの塩の酸化が進行して
いる場合には腐食電位の逆転による腐食の加速などにつ
ながり、一般的に適用されている塗装下地処理と同等の
防錆効果は期待できず、ポーラス化、クラック発生によ
る付着力の低下で、剥離やブリスタが短時間に発生しや
すくなる。On the other hand, a base treatment for forming a chemical conversion coating with phosphate is generally used as a coating base treatment for the purpose of suppressing the diffusion of corrosive substances and the electrochemical rust-preventing effect of metal salts contained in the coating. This is the method applied. However, the chemical conversion coating with phosphate is Mn.
3 (PO 4) 2 · 2MnHPO 4 · 4H 2 O and FeHP
O 4 · 4H 2 O mixed crystal or Zn 3 (PO 4 ) 2
· 4H 2 O and FeHPO 4 · 2~4H 2 O mixed crystal or gamma · Fe 2 of O 3 · FePO 4 · 2H 2 O or F
eHPO 4 · 4~8H 2 O is made from such. These crystals release water of crystallization at 100 to 240 ° C., and oxidative decomposition starts at about 250 ° C. for a manganese phosphate coating and at 130 ° C. for a zinc phosphate coating. Therefore, 20
In the polyethylene powder lining heated and melted at 0 to 300 ° C., not only the formation of a porous material by dehydration, cracking of the phosphoric acid film during dehydration and a decrease in the adhesion of the chemical conversion film, but also Mn and Zn in the phosphoric acid film. If the oxidation of these salts progresses, the corrosion potential will be reversed, leading to accelerated corrosion. The effect cannot be expected, and peeling and blistering are likely to occur in a short time due to a decrease in adhesive force due to formation of a porous material and cracking.
【0008】従って、耐食性、被付着性、耐摩耗性など
に優れたポリエチレンライニングを従来使用してきた常
温付近の環境よりも耐ブリスタ性の面で問題となる高温
環境への適用拡大を図るためには付着性に優れ、かつ耐
食性に優れた下地処理方法の開発が望まれており、技術
的課題になっている。Accordingly, in order to expand the application to a high-temperature environment in which blister resistance is more problematic than in the environment near normal temperature where polyethylene linings excellent in corrosion resistance, adhesion, abrasion resistance, etc. have conventionally been used. There is a demand for the development of a base treatment method which is excellent in adhesion and corrosion resistance, and is a technical problem.
【0009】本発明は上記技術水準に鑑み、かつ上記技
術的課題に応じて、高温環境下でも優れたポリエチレン
ライニングを施工できる下地処理方法を提供しようとす
るものである。The present invention has been made in consideration of the above-mentioned technical level, and has as its object to provide a base treatment method capable of applying an excellent polyethylene lining even in a high-temperature environment in accordance with the above technical problems.
【0010】[0010]
【課題を解決するための手段】本発明はポリエチレン粉
体の溶融温度以上に予備加熱した炭素鋼からなる被ライ
ニング材に該ポリエチレン粉末を供給し、被ライニング
材の熱によって粉末を溶融させ、被ライニング材表面に
連続したポリエチレンの被膜を形成させるライニング方
法において、被ライニング材表面をブラストまたは酸洗
処理したのち、被ライニング材表面を300〜500℃
に加熱し、Fe3 O4 を主体とする被膜を形成させ、次
いでpHが4.5〜6.0であって、CrO3 濃度が
0.005〜0.05wt%のクロム酸水溶液に接触さ
せたのち乾燥することを特徴とするポリエチレン粉体ラ
イニングの下地処理方法である。According to the present invention, the polyethylene powder is supplied to a lining material made of carbon steel preheated to a melting temperature of the polyethylene powder or higher, and the powder is melted by the heat of the lining material. In the lining method of forming a continuous polyethylene film on the surface of the lining material, after blasting or pickling the surface of the lining material, the lining material surface is heated to 300 to 500 ° C.
To form a film mainly composed of Fe 3 O 4 , and then contacted with a chromic acid aqueous solution having a pH of 4.5 to 6.0 and a CrO 3 concentration of 0.005 to 0.05 wt%. An undercoating method for polyethylene powder lining, characterized by drying afterwards.
【0011】[0011]
【作用】本発明は被ライニング材の表面をブラスト処理
または酸洗処理により清浄にしたのち、その面に耐熱、
耐食性に優れ、かつ、付着力にも優れている均一で緻密
なFe3 O4 を主体とする被膜を300〜500℃に被
ライニング材を加熱することで形成させ、更にpHが
4.5〜6.0であって、CrO3 濃度が0.005〜
0.05wt%のクロム酸水溶液と接触させることによ
り、加熱によって形成されたFe3 O4 被膜に生じる微
細なクラックの防食を強化する下地方法である。According to the present invention, after the surface of the material to be lined is cleaned by blasting or pickling, the surface is heat resistant.
A uniform and dense coating mainly composed of Fe 3 O 4 having excellent corrosion resistance and excellent adhesion is formed by heating the material to be lined at 300 to 500 ° C., and the pH is further adjusted to 4.5 to 4.5. 6.0 and the CrO 3 concentration is between 0.005 and
This is a base method for strengthening the corrosion prevention of fine cracks generated in the Fe 3 O 4 coating formed by heating by contacting with a 0.05 wt% chromic acid aqueous solution.
【0012】pHが4.5より低く、CrO3 が0.0
5wt%を越える高い場合には、Fe3 O4 被膜の微細
なクラックに浸透したクロム酸により下地金属がおかさ
れ、Fe3 O4 と下地金属との結合力を弱め、ポリエチ
レンライニング材の耐ブリスタ性が悪くなる。またpH
が6.0を越えて高く、CrO3 が0.005wt%未
満の場合には前記、微細クラック部の下地金属のクロム
による防食効果が低くなる。PH is lower than 4.5 and CrO 3 is less than 0.0
If the content is higher than 5 wt%, chromic acid that has penetrated into fine cracks in the Fe 3 O 4 coating damages the underlying metal, weakens the bonding force between the Fe 3 O 4 and the underlying metal, and resists blistering of the polyethylene lining material. Worse. Also pH
Is higher than 6.0 and the CrO 3 content is less than 0.005 wt%, the corrosion prevention effect of the chromium of the base metal in the fine crack portion becomes low.
【0013】[0013]
【実施例】厚さ3mm、直径120mmの炭素鋼板をオ
ルソケイ酸ソーダ3%溶液に10分間浸漬し脱脂洗浄し
たものを50℃の塩酸5%溶液に10分間浸したのち、
90℃の温水で洗浄したものと、脱脂洗浄後、ショット
ブラストしたブラスト板を製作した。EXAMPLE A carbon steel sheet having a thickness of 3 mm and a diameter of 120 mm was immersed in a 3% solution of sodium orthosilicate for 10 minutes, degreased and washed, and immersed in a 5% solution of hydrochloric acid at 50 ° C. for 10 minutes.
A blast plate washed with warm water at 90 ° C. and a shot-blasted blast plate after degreasing and washing were produced.
【0014】次いでそれらを加熱炉に入れ、300〜5
00℃で30〜50分間加熱処理し、被ライニング材の
表面にFe3 O4 を主体とする被膜を形成した。次いで
常温まで冷却した前記供試材をpHが4.5〜6.0で
あって、CrO3 濃度が0.005〜0.05wt%の
クロム酸水溶液に常温で10秒間浸漬したのち熱風乾燥
した。Then, they are placed in a heating furnace, and 300 to 5
Heat treatment was performed at 00 ° C. for 30 to 50 minutes to form a film mainly composed of Fe 3 O 4 on the surface of the lining material. Next, the test material cooled to room temperature was immersed in a chromic acid aqueous solution having a pH of 4.5 to 6.0 and a CrO 3 concentration of 0.005 to 0.05 wt% at room temperature for 10 seconds, and then dried with hot air. .
【0015】前記、下地処理を行った供試材を250℃
±10℃に熱板上で加熱したのちメルトフローレート
3.0g/10minで平均粒径100μmのポリエチ
レン粉体を前記下地処理をした面に均一に散布し、1m
m厚のポリエチレン膜を形成させた。The test material subjected to the above-mentioned undercoat treatment is heated at 250 ° C.
After heating on a hot plate at ± 10 ° C., a polyethylene powder having an average particle size of 100 μm was evenly sprayed on the surface subjected to the base treatment at a melt flow rate of 3.0 g / 10 min.
An m-thick polyethylene film was formed.
【0016】表1に前記下地処理において、Fe3 O4
被膜形成時の加熱温度及びクロム酸水溶液浸漬における
クロム酸濃度を変えて下地処理した炭素鋼にポリエチレ
ン粉体ライニングした供試材を用いて、ポリエチレンラ
イニング側にpHが0.5の硫酸水溶液を入れて、60
℃に加熱し、ライニングをしていない鋼板側に20℃の
冷却水で冷却した条件下でブリスタが発生するまでの時
間を測定し、その結果をリン酸亜鉛系化成処理面にポリ
エチレン粉体をライニングした参考材にブリスタが発生
するまでの期間との倍率で示した。なお、従来のブラス
ト処理後、ポリエチレン粉末をライニングした参考材は
リン酸亜鉛系化成処理面にポリエチレン粉体をライニン
グした参考材の1/3の期間にブリスタが発生した。Table 1 shows that in the above-mentioned undercoating process, Fe 3 O 4
Using a test material obtained by lining polyethylene powder on carbon steel pretreated by changing the heating temperature during the film formation and the chromic acid concentration in the chromic acid aqueous solution immersion, put a sulfuric acid aqueous solution with a pH of 0.5 on the polyethylene lining side. And 60
℃, and the time until blisters are generated under the condition of cooling with 20 ° C. cooling water on the unlined steel sheet side, and the result is measured by applying the polyethylene powder to the zinc phosphate chemical conversion treated surface. The ratio is shown as a magnification with respect to a period until blisters are generated in the lined reference material. After the conventional blasting treatment, the reference material lined with polyethylene powder generated blisters in the period of 1/3 of the reference material lined with polyethylene powder on the zinc phosphate chemical conversion treated surface.
【0017】[0017]
【表1】 [Table 1]
【0018】[0018]
【発明の効果】本発明の下地処理を適用することによ
り、従来剥離やブリスタ発生が問題となり実用し難かっ
た50〜60℃の環境にポリエチレン粉体ライニングが
適用可能になった。ポリエチレン粉体ライニングは前記
環境条件に用いられる他の樹脂(熱硬化性樹脂)ライニ
ングやゴムライニングに比べて生産コストも低く、樹脂
ライニングやゴムライニングで施工できないような小口
径の配管内面にも施工できる利点もあり、本発明により
ポリエチレン粉体ライニングの適用範囲の拡大が見込ま
れることから、その工業的効果は大きく、かつ長期寿命
確保による信頼性向上効果も大きい。By applying the undercoating treatment of the present invention, the polyethylene powder lining can be applied to an environment of 50 to 60 ° C., which has conventionally been difficult due to peeling and blister generation. Polyethylene powder lining has a lower production cost than other resin (thermosetting resin) linings and rubber linings used in the above-mentioned environmental conditions, and is also applied to the inside of small-diameter pipes that cannot be installed with resin lining or rubber lining Since the present invention is expected to expand the applicable range of the polyethylene powder lining, the present invention has a great industrial effect and a great effect of improving reliability by ensuring a long life.
フロントページの続き (51)Int.Cl.7 識別記号 FI C23C 22/00 C23C 22/00 Z 22/83 22/83 (56)参考文献 特開 昭63−27248(JP,A) 特開 平3−234527(JP,A) 特公 昭46−26843(JP,B1) (58)調査した分野(Int.Cl.7,DB名) B05D 1/00 - 7/26 C23C 22/00 - 22/86 Continuation of the front page (51) Int.Cl. 7 Identification code FI C23C 22/00 C23C 22/00 Z 22/83 22/83 (56) References JP-A-63-27248 (JP, A) JP-A-3 -234527 (JP, A) JP 46-26843 (JP, B1) (58) Fields investigated (Int. Cl. 7 , DB name) B05D 1/00-7/26 C23C 22/00-22/86
Claims (1)
加熱した炭素鋼からなる被ライニング材に該ポリエチレ
ン粉末を供給し、被ライニング材の熱によって粉末を溶
融させ、被ライニング材表面に連続したポリエチレンの
被膜を形成させるライニング方法において、被ライニン
グ材表面をブラストまたは酸洗処理したのち、被ライニ
ング材表面を300〜500℃に加熱し、Fe3 O4 を
主体とする被膜を形成させ、次いでpHが4.5〜6.
0であって、CrO3 濃度が0.005〜0.05wt
%のクロム酸水溶液に接触させたのち乾燥することを特
徴とするポリエチレン粉体ライニングの下地処理方法。1. The polyethylene powder is supplied to a lining material made of carbon steel which is preheated to a melting temperature of the polyethylene powder or higher, and the powder is melted by the heat of the lining material, so that the polyethylene is continuous on the surface of the lining material. In the lining method of forming a film of the above, after blasting or pickling the surface of the material to be lined, the surface of the material to be lined is heated to 300 to 500 ° C. to form a film mainly composed of Fe 3 O 4 , Is 4.5-6.
0 and the CrO 3 concentration is 0.005 to 0.05 wt.
% Chromic acid aqueous solution, followed by drying.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10763892A JP2999059B2 (en) | 1992-04-27 | 1992-04-27 | Surface treatment method for polyethylene powder lining |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10763892A JP2999059B2 (en) | 1992-04-27 | 1992-04-27 | Surface treatment method for polyethylene powder lining |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH05301072A JPH05301072A (en) | 1993-11-16 |
| JP2999059B2 true JP2999059B2 (en) | 2000-01-17 |
Family
ID=14464271
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP10763892A Expired - Fee Related JP2999059B2 (en) | 1992-04-27 | 1992-04-27 | Surface treatment method for polyethylene powder lining |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2999059B2 (en) |
-
1992
- 1992-04-27 JP JP10763892A patent/JP2999059B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JPH05301072A (en) | 1993-11-16 |
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