JPH11263926A - Epoxy powder coating composition for coating of outer surface of cast iron pipe and outer surface-coated cast iron pipe - Google Patents

Epoxy powder coating composition for coating of outer surface of cast iron pipe and outer surface-coated cast iron pipe

Info

Publication number
JPH11263926A
JPH11263926A JP6819298A JP6819298A JPH11263926A JP H11263926 A JPH11263926 A JP H11263926A JP 6819298 A JP6819298 A JP 6819298A JP 6819298 A JP6819298 A JP 6819298A JP H11263926 A JPH11263926 A JP H11263926A
Authority
JP
Japan
Prior art keywords
cast iron
coating
iron pipe
epoxy
powder coating
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
Application number
JP6819298A
Other languages
Japanese (ja)
Other versions
JP3572332B2 (en
Inventor
Takaaki Deguchi
隆亮 出口
Kazuhito Hanano
一仁 花野
Masahiko Saito
昌彦 斉藤
Yoshisada Michiura
吉貞 道浦
Norio Nakamura
典生 中村
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kurimoto Ltd
Nippon Paint Co Ltd
Original Assignee
Kurimoto Ltd
Nippon Paint Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Kurimoto Ltd, Nippon Paint Co Ltd filed Critical Kurimoto Ltd
Priority to JP06819298A priority Critical patent/JP3572332B2/en
Publication of JPH11263926A publication Critical patent/JPH11263926A/en
Application granted granted Critical
Publication of JP3572332B2 publication Critical patent/JP3572332B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16LPIPES; JOINTS OR FITTINGS FOR PIPES; SUPPORTS FOR PIPES, CABLES OR PROTECTIVE TUBING; MEANS FOR THERMAL INSULATION IN GENERAL
    • F16L58/00Protection of pipes or pipe fittings against corrosion or incrustation
    • F16L58/02Protection of pipes or pipe fittings against corrosion or incrustation by means of internal or external coatings
    • F16L58/04Coatings characterised by the materials used

Abstract

PROBLEM TO BE SOLVED: To obtain an epoxy powder coating composition for coating of the outer surface of a cast iron pipe capable of preventing any exfoliations and swells in the damaged or defective sections of the coating and excellent in safety to human and the environment, and to provide the outer surface-coated cast iron pipes. SOLUTION: This composition comprises (A) a bisphenol A type epoxy resin having a melting point of 75 to 128 deg.C and epoxy equivalent of 600 to 2,200 g/eq, (B) a setting agent of a composition of the formula ((m) is an integer of 1 to 4) having a mean phenolic hydroxyl equivalent of 200 to 800 g/eq, (C) at least one of imidazole-based and imidazoline-based setting-accelerators, and (D) a burnt plaster.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、鋳鉄管外面塗装用
エポキシ粉体塗料組成物及び外面塗装鋳鉄管に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an epoxy powder coating composition for coating an outer surface of a cast iron tube and an outer surface coated cast iron tube.

【0002】[0002]

【従来の技術】鋳鉄管類は、従来より、上下水道、工業
用水道、農業用水、ガス用等の配管材として幅広く使用
されている。鋳鉄管類は、形状により、直管、異形管、
押輪等の接合部品に分類される。本明細書においては、
これらの接合部品を総称して、鋳鉄管という。
2. Description of the Related Art Cast iron pipes have been widely used as piping materials for water and sewage, industrial water, agricultural water, gas and the like. Cast iron pipes, depending on the shape, straight pipe, deformed pipe,
It is classified as a joint part such as a pressing wheel. In this specification,
These joints are collectively called cast iron tubes.

【0003】鋳鉄管の外面には、通常、エポキシ系、ア
クリル系、ポリエステル系等の常温乾燥溶剤型防食塗料
が塗装されている。近年、鋳鉄管内面の焼き付け時の余
熱の有効利用や、塗膜の乾燥硬化養生時間の短縮、養生
場所の削減等の塗装工程の合理化や、塗装作業環境の改
善を目的として、常温乾燥溶剤型防食塗料のほか、エポ
キシ粉体塗料も用いられるようになった。
[0003] The outer surface of a cast iron pipe is usually coated with a normal temperature solvent-based anticorrosive paint such as an epoxy-based, acrylic-based, or polyester-based paint. In recent years, room temperature dry solvent type has been used for the purpose of effective utilization of residual heat when baking the inner surface of cast iron pipes, shortening the drying and curing time of the coating film, streamlining the coating process such as reducing the curing place, and improving the coating work environment. In addition to anticorrosive paints, epoxy powder paints have also been used.

【0004】鋳鉄管の外面の塗装を行う場合、突起部や
端部では、均一な塗装が困難であり、一般的には、塗膜
の膜厚が不充分となり、ピンホール等の欠陥を生じやす
い。このような欠陥が存在すると、その箇所から水が進
入し、耐食性が不充分となる。また、鋳鉄管の外面は、
輸送時、埋設時に衝撃を受けやすく、このような衝撃に
よって、傷がつきやすい。このため、鋳鉄管の外面の塗
装に適用する塗料においては、塗膜の欠陥部や損傷部の
耐食性の改良が課題となっている。
When the outer surface of a cast iron tube is coated, it is difficult to apply a uniform coating on the protrusions and ends, and generally, the coating film thickness is insufficient, and defects such as pinholes occur. Cheap. If such a defect exists, water enters from that location, and the corrosion resistance becomes insufficient. Also, the outer surface of the cast iron tube
During transportation and burial, it is susceptible to impacts, and such impacts can easily cause damage. For this reason, in the coating applied to the coating of the outer surface of the cast iron pipe, improvement of the corrosion resistance of a defective portion or a damaged portion of the coating film has been a problem.

【0005】鋳鉄管外面の塗膜の欠陥部、損傷部におい
ては、大気中や雨水中に含まれる海塩粒子等の電解質
や、埋設箇所付近に存在する電解質の作用により、鋳鉄
管表面に錆が発生する。このとき、塗膜の欠陥部、損傷
部等の鋳鉄管表面の一部が微小アノードとなり、欠陥
部、損傷部の近傍にカソード部位が形成される。
[0005] Defects and damaged portions of the coating film on the outer surface of the cast iron pipe cause rust on the surface of the cast iron pipe due to the action of electrolytes such as sea salt particles contained in the atmosphere or rainwater and electrolytes present near the buried area. Occurs. At this time, a part of the surface of the cast iron tube such as a defective portion or a damaged portion of the coating film becomes a minute anode, and a cathode site is formed near the defective portion or the damaged portion.

【0006】形成されたカソード部位では、水酸化物イ
オンが生成し、この水酸化物イオンの作用によって、鋳
鉄面と塗膜との密着性が低下するため、塗膜の剥離やフ
クレが発生する。本明細書中、このような剥離やフクレ
を「カソード剥離」、「カソードフクレ」と称する。こ
れらの現象が拡大し、水溶解電解質が剥離部、フクレ部
に容易に浸透する結果、更に剥離部やフクレ部を拡大さ
せる問題があった。
At the formed cathode portion, hydroxide ions are generated, and the action of the hydroxide ions reduces the adhesion between the cast iron surface and the coating film, thereby causing peeling and blistering of the coating film. . In the present specification, such peeling or blistering is referred to as “cathode peeling” or “cathode blister”. These phenomena are magnified, and the water-soluble electrolyte easily penetrates into the peeling portion and blister portion, resulting in a problem that the peeling portion and blister portion are further enlarged.

【0007】このような塗膜の剥離やフクレの発生を抑
制するために、従来より、塗料にストロンチウムクロメ
ート等の防錆顔料の塗料への添加が考えられたが、スト
ロンチウムクロメート等の防錆顔料が、人体や環境に悪
影響を及ぼすおそれがあるため、使用することができな
かった。
In order to suppress the peeling of the coating film and the occurrence of blisters, it has heretofore been considered to add a rust preventive pigment such as strontium chromate to the paint. However, a rust preventive pigment such as strontium chromate has been considered. However, it could not be used because it might adversely affect the human body and the environment.

【0008】特開平6−228466号公報には、硫酸
又は金属酸化物を担持させた固体超強酸を使用して、カ
ソード部位で生成する水酸化物イオンを消費させ、フク
レを防ぐ塗料が開示されている。しかしながら、この技
術では、製造時において固体超強酸の取り扱いが難し
く、また、コスト的にも不利である。また、硫酸を担持
させているため、塗料の変質等のおそれもある。
Japanese Patent Application Laid-Open No. 6-228466 discloses a paint that uses a solid superacid carrying sulfuric acid or a metal oxide to consume hydroxide ions generated at the cathode site, thereby preventing blistering. ing. However, with this technique, it is difficult to handle the solid superacid during production, and it is disadvantageous in terms of cost. In addition, since sulfuric acid is carried, there is a possibility that the paint may deteriorate.

【0009】従って、鋳鉄管外面の塗装においては、安
全性に優れ、安価に製造することができ、また、耐食
性、耐衝撃性、可撓性等の鋳鉄管外面の塗膜として要求
される性能を有する塗膜を形成することができる塗料の
開発が望まれている。
Therefore, in coating the outer surface of the cast iron tube, it is excellent in safety and can be manufactured at a low cost, and the performance required as a coating film on the outer surface of the cast iron tube such as corrosion resistance, impact resistance and flexibility. There is a demand for the development of a paint capable of forming a coating film having the following.

【0010】[0010]

【発明が解決しようとする課題】本発明は、上記に鑑
み、塗膜の損傷部や欠陥部において、剥離やフクレを生
じさせることがなく、人体や環境に対する安全性に優
れ、鋳鉄管への付着性が良好であり、安価にかつ容易に
製造することができ、低温で焼き付けを行うことができ
る鋳鉄管外面塗装用エポキシ粉体塗料組成物、及び、耐
食性、耐衝撃性、可撓性に優れた塗膜で外面を塗装され
た外面塗装鋳鉄管を提供することを目的とするものであ
る。
SUMMARY OF THE INVENTION In view of the above, the present invention does not cause peeling or blistering at a damaged or defective portion of a coating film, is excellent in safety to the human body and the environment, and is suitable for a cast iron pipe. Epoxy powder coating composition for outer coating of cast iron pipe, which has good adhesion, can be easily manufactured at low cost and can be baked at low temperature, and has excellent corrosion resistance, impact resistance and flexibility An object of the present invention is to provide an externally coated cast iron pipe whose outer surface is coated with an excellent coating film.

【0011】[0011]

【課題を解決するための手段】本発明は、軟化点が75
〜128℃であり、エポキシ当量が600〜2200g
/eqであるビスフェノールA型エポキシ樹脂(A)、
下記一般式(1);
According to the present invention, the softening point is 75%.
~ 128 ° C, epoxy equivalent is 600 ~ 2200g
/ Eq bisphenol A type epoxy resin (A),
The following general formula (1);

【0012】[0012]

【化2】 Embedded image

【0013】(式中、mは、1〜4の整数を表す。)で
表される化合物であって、平均フェノール性水酸基当量
が200〜800g/eqである硬化剤(B)、イミダ
ゾール系硬化促進剤及びイミダゾリン系硬化促進剤のう
ち少なくとも1種の硬化促進剤(C)、並びに、焼セッ
コウ(D)からなる鋳鉄管外面塗装用エポキシ粉体塗料
組成物であって、上記硬化剤(B)のフェノール性水酸
基の量は、上記ビスフェノールA型エポキシ樹脂(A)
のエポキシ1当量に対して、0.5〜1.2当量であ
り、上記硬化促進剤(C)の配合量は、上記硬化剤
(B)の配合量に対して、0.1〜15.0重量%であ
り、かつ、上記焼セッコウ(D)の配合量は、鋳鉄管外
面塗装用エポキシ粉体塗料組成物に対して、2〜50重
量%となるように配合されるものである鋳鉄管外面塗装
用エポキシ粉体塗料組成物である。また、本発明は、上
記本発明の鋳鉄管外面塗装用エポキシ粉体塗料組成物を
用いて塗装された外面塗装鋳鉄管である。以下に本発明
を詳述する。
A curing agent (B) having an average phenolic hydroxyl group equivalent of 200 to 800 g / eq, and an imidazole-based curing compound, wherein m is an integer of 1 to 4; An epoxy powder coating composition for exterior coating of cast iron pipes, comprising at least one curing accelerator (C) among an accelerator and an imidazoline-based curing accelerator, and calcined gypsum (D), wherein the curing agent (B )), The amount of the phenolic hydroxyl group is determined by the above-mentioned bisphenol A type epoxy resin (A).
Is 0.5 to 1.2 equivalents with respect to 1 equivalent of the epoxy, and the compounding amount of the curing accelerator (C) is 0.1 to 15.2 equivalents with respect to the compounding amount of the curing agent (B). 0% by weight, and the amount of the calcined gypsum (D) is 2 to 50% by weight based on the epoxy powder coating composition for coating the outer surface of a cast iron pipe. It is an epoxy powder coating composition for coating the outer surface of a tube. Further, the present invention is an externally coated cast iron pipe coated using the epoxy powder coating composition for externally coating a cast iron pipe of the present invention. Hereinafter, the present invention will be described in detail.

【0014】本発明の鋳鉄管外面塗装用エポキシ粉体塗
料組成物は、軟化点が75〜128℃であり、エポキシ
当量が600〜2200g/eqであるビスフェノール
A型エポキシ樹脂(A)、下記一般式(1);
The epoxy powder coating composition for coating the outer surface of a cast iron pipe of the present invention has a softening point of 75 to 128 ° C. and an epoxy equivalent of 600 to 2200 g / eq. Formula (1);

【0015】[0015]

【化3】 Embedded image

【0016】(式中、mは、1〜4の整数を表す。)で
表される化合物であって、平均フェノール性水酸基当量
が200〜800g/eqである硬化剤(B)、イミダ
ゾール系硬化促進剤及びイミダゾリン系硬化促進剤のう
ち少なくとも1種の硬化促進剤(C)、並びに、焼セッ
コウ(D)からなる。
A curing agent (B) having a mean phenolic hydroxyl group equivalent of 200 to 800 g / eq, wherein the m is an integer of 1 to 4; It comprises at least one of a curing accelerator and an imidazoline curing accelerator (C), and calcined gypsum (D).

【0017】上記ビスフェノールA型エポキシ樹脂
(A)は、軟化点が75〜128℃である。75℃未満
であると、粉体塗料の貯蔵中に粉体塗料同士の融着が起
こりやすく、128℃を超えると、溶融粘度が高くな
り、低温での焼き付け、又は、余熱を利用した塗膜形成
の仕上がり性が低下するので、上記範囲に限定される。
好ましくは、90〜110℃である。
The bisphenol A type epoxy resin (A) has a softening point of 75 to 128 ° C. If the temperature is lower than 75 ° C., the powder coatings are liable to be fused to each other during storage of the powder coating. If the temperature exceeds 128 ° C., the melt viscosity increases, and the coating is baked at a low temperature or using the residual heat. Since the finish of formation is reduced, the content is limited to the above range.
Preferably, it is 90 to 110 ° C.

【0018】上記ビスフェノールA型エポキシ樹脂
(A)は、エポキシ当量が600〜2200g/eqで
ある。600g/eq未満であると、一般に分子量が小
さくなり、軟化温度が低くなりすぎ、2200g/eq
を超えると、一般に分子量が大きくなり、軟化温度が高
くなりすぎるので、上記範囲に限定される。好ましく
は、650〜1100g/eqである。
The bisphenol A type epoxy resin (A) has an epoxy equivalent of 600 to 2200 g / eq. When it is less than 600 g / eq, generally the molecular weight becomes small and the softening temperature becomes too low, and 2200 g / eq
If it exceeds, the molecular weight is generally increased and the softening temperature is too high, so that it is limited to the above range. Preferably, it is 650 to 1100 g / eq.

【0019】上記ビスフェノールA型エポキシ樹脂
(A)としては、軟化点が75〜128℃であり、エポ
キシ当量が600〜2200g/eqであるものであれ
ば特に限定されず、例えば、ビスフェノールA〔2,2
−ビス(4−ヒドロキシフェニル)プロパン〕とエピク
ロルヒドリン等のエピハロヒドリンとを反応させて、一
旦低分子量のエポキシ樹脂を製造した後、更にビスフェ
ノールAを付加重合させて、所望の分子量に調整する2
段法により得られるもの等を挙げることができる。
The bisphenol A type epoxy resin (A) is not particularly limited as long as it has a softening point of 75 to 128 ° C. and an epoxy equivalent of 600 to 2200 g / eq. , 2
-Bis (4-hydroxyphenyl) propane] and an epihalohydrin such as epichlorohydrin to produce a low-molecular-weight epoxy resin, and then to add-polymerize bisphenol A to adjust to a desired molecular weight.
Those obtained by the step method can be exemplified.

【0020】上記ビスフェノールA型エポキシ樹脂
(A)としては、市販されているものも使用することが
できる。具体的には、例えば、エポトートYD−014
(エポキシ当量900〜1000g/eq、軟化点91
〜102℃、東都化成社製)、エポトートYD−017
(エポキシ当量1750〜2100g/eq、軟化点1
17〜127℃、東都化成社製)、エポトートYD−9
04(エポキシ当量900〜1000g/eq、軟化点
96〜107℃、東都化成社製)、エポトートYD−9
07(エポキシ当量1300〜1700g/eq、軟化
点117〜127℃、東都化成社製)、エピコート10
03F(エポキシ当量700〜800g/eq、軟化点
約96℃、油化シェルエポキシ社製)、エピコート10
04F(エポキシ当量875〜975g/eq、軟化点
約103℃、油化シェルエポキシ社製)、エピコート1
005F(エポキシ当量950〜1050g/eq、軟
化点約107℃、油化シェルエポキシ社製)、アラルダ
イトXAC5007(エポキシ当量600〜700g/
eq、軟化点約90℃、日本チバガイギー社製)、アラ
ルダイトGT7004(エポキシ当量730〜830g
/eq、軟化点約100℃、日本チバガイギー社製)、
アラルダイトGT7097(エポキシ当量1650〜2
000g/eq、軟化点約120℃、日本チバガイギー
社製)等を挙げることができる。これらは単独で使用し
てもよく、2種以上を併用してもよい。なかでも、低温
焼き付けでの仕上がり性(レベリング性)の点から、エ
ピコート1003F、エピコート1005F等が好まし
い。
As the bisphenol A type epoxy resin (A), a commercially available one can be used. Specifically, for example, Epotote YD-014
(Epoxy equivalent: 900 to 1000 g / eq, softening point: 91
〜10102 ° C., manufactured by Toto Kasei Co., Ltd.), Epototo YD-017
(Epoxy equivalent 1750-2100 g / eq, softening point 1
17-127 ° C, manufactured by Toto Kasei Co., Ltd.), Epototo YD-9
04 (epoxy equivalent: 900-1000 g / eq, softening point: 96-107 ° C, manufactured by Toto Kasei Co., Ltd.), Epototo YD-9
07 (epoxy equivalent 1300-1700 g / eq, softening point 117-127 ° C, manufactured by Toto Kasei Co., Ltd.), Epicoat 10
03F (epoxy equivalent: 700-800 g / eq, softening point: about 96 ° C, manufactured by Yuka Shell Epoxy), Epicoat 10
04F (epoxy equivalent: 875-975 g / eq, softening point: about 103 ° C., manufactured by Yuka Shell Epoxy), Epicoat 1
005F (epoxy equivalent: 950-1050 g / eq, softening point: about 107 ° C., manufactured by Yuka Shell Epoxy), Araldite XAC5007 (epoxy equivalent: 600-700 g /
eq, softening point of about 90 ° C, manufactured by Nippon Ciba Geigy), Araldite GT7004 (epoxy equivalent 730-830 g)
/ Eq, softening point about 100 ° C, manufactured by Nippon Ciba Geigy)
Araldite GT7097 (epoxy equivalent 1650-2
000 g / eq, a softening point of about 120 ° C., manufactured by Ciba-Geigy Japan). These may be used alone or in combination of two or more. Among them, Epicoat 1003F, Epicoat 1005F, and the like are preferable from the viewpoint of the finish (leveling property) in low-temperature baking.

【0021】本発明で使用される硬化剤(B)は、上記
ビスフェノールA型エポキシ樹脂(A)の硬化剤として
使用される成分であり、下記一般式(1)で表される化
合物である。
The curing agent (B) used in the present invention is a component used as a curing agent for the bisphenol A type epoxy resin (A), and is a compound represented by the following general formula (1).

【0022】[0022]

【化4】 Embedded image

【0023】式中、mは、1〜4の整数を表す。上記m
が1未満であると、以下に詳述するように、原料として
ビスフェノールAを使用する場合には、存在することが
できず、mが4を超えると、合成時に反応が進みすぎ
て、合成が困難となるので、上記範囲に限定される。
In the formula, m represents an integer of 1 to 4. The above m
Is less than 1, when bisphenol A is used as a raw material, it cannot exist, as described in detail below. When m exceeds 4, the reaction proceeds too much during the synthesis, and the synthesis proceeds. Since it becomes difficult, it is limited to the above range.

【0024】上記一般式(1)で表される化合物として
は特に限定されず、例えば、ビスフェノールA型エポキ
シ樹脂とビスフェノールAとの反応により得られるもの
等を挙げることができる。
The compound represented by the general formula (1) is not particularly limited, and examples thereof include compounds obtained by reacting bisphenol A type epoxy resin with bisphenol A.

【0025】上記硬化剤(B)は、フェノール性水酸基
当量が200〜800g/eqである。200g/eq
未満であると、塗料の軟化点が低下し、貯蔵中に粉体塗
料同士のブロッキングが起こりやすくなり、800g/
eqを超えると、反応性が低下し、低温硬化が困難にな
るので、上記範囲に限定される。
The curing agent (B) has a phenolic hydroxyl equivalent of 200 to 800 g / eq. 200g / eq
If it is less than 1, the softening point of the coating material is lowered, and the powder coating material is liable to be blocked during storage.
If it exceeds eq, the reactivity will decrease and low-temperature curing will be difficult, so it will be limited to the above range.

【0026】上記硬化剤(B)としては、市販されてい
るものを使用してもよい。具体的には、例えば、TH−
4100(フェノール性水酸基当量約725g/eq、
軟化点約110℃、東都化成社製)、エピキュア171
(フェノール性水酸基当量200〜286g/eq、軟
化点約80℃、油化シェル社製)、エピキュア170
(フェノール性水酸基当量286〜400g/eq、軟
化点約90℃、油化シェル社製)等を挙げることができ
る。これらは単独で使用してもよく、2種以上を併用し
てもよい。なかでも、貯蔵安定性、仕上がり性(レベリ
ング性)の点から、エピキュア170が好ましい。
As the curing agent (B), a commercially available one may be used. Specifically, for example, TH-
4100 (phenolic hydroxyl group equivalent of about 725 g / eq,
Softening point about 110 ° C, manufactured by Toto Kasei Co., Ltd.), EpiCure 171
(Phenolic hydroxyl equivalent: 200 to 286 g / eq, softening point: about 80 ° C., manufactured by Yuka Shell Co.), Epicure 170
(Phenolic hydroxyl equivalent: 286 to 400 g / eq, softening point: about 90 ° C., manufactured by Yuka Shell Co., Ltd.). These may be used alone or in combination of two or more. Above all, Epicure 170 is preferable in terms of storage stability and finish (leveling property).

【0027】本発明において、上記硬化剤(B)には、
フェノール性水酸基当量200〜800g/eqの範囲
内で、ビスフェノールAの未反応物が含まれていてもよ
い。上記ビスフェノールAの含有率は、上記硬化剤
(B)及びビスフェノールAの合計に対して、多い場合
で30重量%である。
In the present invention, the curing agent (B) includes:
Unreacted bisphenol A may be contained within the range of the phenolic hydroxyl group equivalent of 200 to 800 g / eq. The content of the bisphenol A is at most 30% by weight based on the total of the curing agent (B) and the bisphenol A.

【0028】上記硬化剤(B)のフェノール性水酸基の
量は、上記ビスフェノールA型エポキシ樹脂(A)のエ
ポキシ1当量に対して、0.5〜1.2当量である。
0.5当量未満であると、充分な硬化物が得られず、耐
衝撃性等の機械的強度が不良となり、1.2当量を超え
ると、未反応の硬化剤が塗膜中に残存し、硬化性が不良
となるので、上記範囲に限定される。好ましくは、0.
5〜1.0当量である。
The amount of the phenolic hydroxyl group of the curing agent (B) is 0.5 to 1.2 equivalents to 1 equivalent of the epoxy of the bisphenol A type epoxy resin (A).
If the amount is less than 0.5 equivalent, a sufficient cured product cannot be obtained, and mechanical strength such as impact resistance becomes poor. If the amount exceeds 1.2 equivalents, an unreacted curing agent remains in the coating film. , The curability becomes poor, so that it is limited to the above range. Preferably, 0.
5 to 1.0 equivalent.

【0029】本発明においては、上記ビスフェノールA
型エポキシ樹脂(A)の硬化剤として、鋳鉄管への付着
性の向上、耐食性の向上のために、上記硬化剤(B)と
ジシアンジアミドとを併用してもよい。
In the present invention, the above bisphenol A
As a curing agent for the epoxy resin (A), the curing agent (B) and dicyandiamide may be used in combination for the purpose of improving adhesion to a cast iron pipe and improving corrosion resistance.

【0030】本発明で使用される硬化促進剤(C)は、
イミダゾール系硬化促進剤及びイミダゾリン系硬化促進
剤のうち少なくとも1種である。本発明において、上記
硬化促進剤(C)は、低温焼き付け性をより良好にする
ために使用される。上記イミダゾール系硬化促進剤及び
イミダゾリン系硬化促進剤は、それぞれ下記一般式
(2)及び下記一般式(3)で表される化合物である。
The curing accelerator (C) used in the present invention comprises:
At least one of an imidazole-based curing accelerator and an imidazoline-based curing accelerator. In the present invention, the curing accelerator (C) is used to improve low-temperature baking properties. The imidazole-based curing accelerator and the imidazoline-based curing accelerator are compounds represented by the following general formulas (2) and (3), respectively.

【0031】[0031]

【化5】 Embedded image

【0032】式中、R1 は、水素原子、炭素数1〜17
のアルキル基、又は、フェニル基を表す。R2 は、水素
原子、又は、メチル基を表す。
In the formula, R 1 is a hydrogen atom, having 1 to 17 carbon atoms.
Represents an alkyl group or a phenyl group. R 2 represents a hydrogen atom or a methyl group.

【0033】上記炭素数1〜17のアルキル基としては
特に限定されず、例えば、メチル基、エチル基、n−プ
ロピル基、i−プロピル基等を挙げることができる。
The alkyl group having 1 to 17 carbon atoms is not particularly limited, and examples thereof include a methyl group, an ethyl group, an n-propyl group and an i-propyl group.

【0034】上記イミダゾール系硬化促進剤としては特
に限定されず、市販されているものを使用してもよい。
具体的には、例えば、2MZ(2−メチルイミダゾー
ル、四国化成工業社製)、2PZ(2−フェニルイミダ
ゾール、四国化成工業社製)、C11Z(2−ウンデシル
イミダゾール、四国化成工業社製)、C17Z(2−ヘプ
タデシルイミダゾール、四国化成工業社製)等を挙げる
ことができる。これらは単独で使用してもよく、2種以
上を併用してもよい。なかでも、硬化促進機能の点か
ら、2MZが好ましい。
The imidazole-based curing accelerator is not particularly limited, and a commercially available one may be used.
Specifically, for example, 2MZ (2-methylimidazole, manufactured by Shikoku Chemicals), 2PZ (2-phenylimidazole, manufactured by Shikoku Chemicals), C 11 Z (2-undecylimidazole, manufactured by Shikoku Chemicals) ), C 17 Z (2-heptadecyl imidazole, manufactured by Shikoku Chemicals) and the like. These may be used alone or in combination of two or more. Among them, 2MZ is preferable from the viewpoint of the curing acceleration function.

【0035】上記イミダゾリン系硬化促進剤としては特
に限定されず、市販されているものを使用してもよい。
具体的には、例えば、2MZL(2−メチルイミダゾリ
ン、四国化成工業社製)、2E・4MZL(2−エチル
−4−メチルイミダゾリン、四国化成工業社製)等を挙
げることができる。これらは単独で使用してもよく、2
種以上を併用してもよい。
The imidazoline curing accelerator is not particularly limited, and commercially available ones may be used.
Specifically, for example, 2MZL (2-methylimidazoline, manufactured by Shikoku Kasei Kogyo), 2E · 4MZL (2-ethyl-4-methylimidazoline, manufactured by Shikoku Kasei Kogyo) and the like can be mentioned. These may be used alone,
More than one species may be used in combination.

【0036】上記硬化促進剤(C)は、上記硬化剤
(B)の配合量に対して、0.1〜15.0重量%とな
るように配合される。0.1重量%未満であると、硬化
が促進されず、15.0重量%を超えると、反応性が高
くなりすぎ、ブロッキングが発生しやすくなり、貯蔵安
定性が不良となるので、上記範囲に限定される。好まし
くは、0.5〜10.0重量%である。
The curing accelerator (C) is blended in an amount of 0.1 to 15.0% by weight based on the blending amount of the curing agent (B). If the amount is less than 0.1% by weight, curing is not promoted. If the amount exceeds 15.0% by weight, the reactivity becomes too high, blocking tends to occur, and storage stability becomes poor. Is limited to Preferably, it is 0.5 to 10.0% by weight.

【0037】本発明で使用される焼セッコウ(D)は、
顔料成分として用いられるものであり、硫酸カルシウム
(CaSO4 )の水和物のうち、化学式CaSO4 ・1
/2H2 Oで表される化合物である。上記焼セッコウを
用いることにより、上記水酸化物イオンによって発生す
るカソード剥離、カソードフクレを防止することができ
る。このような効果は、上述した硫酸カルシウムの水和
物のうち、上記焼セッコウのみに見られるものである。
The gypsum (D) used in the present invention is:
Is intended to be used as a pigment component, of the hydrates of calcium sulfate (CaSO 4), the chemical formula CaSO 4 · 1
/ 2H 2 O. By using the calcined gypsum, it is possible to prevent cathode peeling and cathode blistering caused by the hydroxide ions. Such an effect is found only in the calcined gypsum among the above-mentioned calcium sulfate hydrates.

【0038】上記焼セッコウ(D)は、鋳鉄管外面塗装
用エポキシ粉体塗料組成物に対して、2〜50重量%と
なるように配合される。2重量%未満であると、得られ
る塗膜の剥離やフクレを防止する性能が充分ではなく、
50重量%を超えると、溶融粘度が高くなり、連続塗膜
の形成が困難となる傾向が生じ、仕上がり性が低下する
ので、上記範囲に限定される。好ましくは、5〜30重
量%である。
The calcined gypsum (D) is blended in an amount of 2 to 50% by weight based on the epoxy powder coating composition for coating the outer surface of a cast iron pipe. If it is less than 2% by weight, the performance of preventing peeling and blistering of the obtained coating film is not sufficient,
If it exceeds 50% by weight, the melt viscosity will be high, and the formation of a continuous coating film will tend to be difficult, and the finish will be poor. Preferably, it is 5 to 30% by weight.

【0039】本発明の鋳鉄管外面塗装用エポキシ粉体塗
料組成物には、更に、炭酸カルシウム、硫酸バリウム、
シリカ等の体質顔料等の無機質充填剤等を配合してもよ
い。無機質充填剤の配合量は、上記焼セッコウ(D)と
の合計量として、鋳鉄管外面塗装用エポキシ粉体塗料組
成物に対して50重量%以下であることが仕上がり性の
点から好ましい。
The epoxy powder coating composition for coating the outer surface of a cast iron pipe of the present invention further comprises calcium carbonate, barium sulfate,
An inorganic filler such as an extender such as silica may be blended. The amount of the inorganic filler to be added is preferably 50% by weight or less based on the epoxy powder coating composition for coating the outer surface of a cast iron pipe as the total amount with the calcined gypsum (D) from the viewpoint of finishability.

【0040】また、本発明の鋳鉄管外面塗装用エポキシ
粉体塗料組成物には、更に、カーボンブラック、チタン
白、ベンガラ等の各種焼成着色顔料;溶融時の流動調整
剤、はじき防止剤;石油樹脂等の熱可塑性樹脂等を配合
してもよい。
The epoxy powder coating composition for coating the outer surface of a cast iron pipe of the present invention further comprises various calcined coloring pigments such as carbon black, titanium white, red iron oxide, etc .; a flow regulator at the time of melting; A thermoplastic resin such as a resin may be blended.

【0041】本発明の鋳鉄管外面塗装用エポキシ粉体塗
料組成物は、低温硬化性を良好にするために、必要に応
じて、ビスフェノールA型エポキシ樹脂(A)、硬化剤
(B)及び硬化促進剤(C)の存在下で、前駆反応を行
っていてもよい。
The epoxy powder coating composition for coating the outer surface of a cast iron pipe according to the present invention may optionally contain a bisphenol A type epoxy resin (A), a curing agent (B) and a curing agent in order to improve the low-temperature curability. The precursor reaction may be performed in the presence of the accelerator (C).

【0042】上記前駆反応は、粉体の状態にすることが
できる範囲内で予め粉体塗料組成物を反応させて、造膜
過程で反応が困難であるために残存しやすい粉体塗料組
成物中の未反応官能基をできる限り少なくしておき、低
温焼き付けを可能にするために行われるものである。換
言すれば、反応に関与する官能基の反応度を高めて、硬
化塗膜の性能を最大に発揮させるものである。
In the precursor reaction, the powder coating composition is preliminarily reacted within a range that can be converted into a powder state, and the powder coating composition which is difficult to react during the film forming process and easily remains is formed. This is performed in order to keep unreacted functional groups in the resin as small as possible and to enable low-temperature baking. In other words, the reactivity of the functional group involved in the reaction is increased to maximize the performance of the cured coating film.

【0043】本発明の鋳鉄管外面塗装用エポキシ粉体塗
料組成物は、上記前駆反応を行う場合、ISO 813
0−6の方法での200℃加熱時の塗料のゲルタイムが
10〜40秒に調整されていることが好ましい。10秒
未満であると、反応が進みすぎて溶融粘度が高くなり、
鋳鉄管への付着性及び塗膜外観が不良となり、40秒を
超えると、期待した低温硬化性が不充分となる。
The epoxy powder coating composition for coating the outer surface of a cast iron pipe according to the present invention, when subjected to the above-mentioned precursor reaction, is subjected to ISO 813
It is preferable that the gel time of the paint when heated at 200 ° C. by the method of 0-6 is adjusted to 10 to 40 seconds. If the time is less than 10 seconds, the reaction proceeds too much and the melt viscosity increases,
Adhesion to the cast iron pipe and appearance of the coating film become poor, and if it exceeds 40 seconds, the expected low-temperature curability becomes insufficient.

【0044】本発明の鋳鉄管外面塗装用エポキシ粉体塗
料組成物は、鋳鉄管の外面の塗装に適用される。塗装方
法としては特に限定されず、例えば、静電粉体塗装、負
帯電静電塗装(コロナ)、摩擦帯電静電塗装(トリ
ボ)、流動浸漬塗装等の通常の粉体塗料の塗装方法とし
て用いられている方法等を挙げることができる。上記塗
装は、乾燥膜厚が60〜200μmとなるように行うこ
とが好ましい。
The epoxy powder coating composition for coating the outer surface of a cast iron pipe of the present invention is applied to coating the outer surface of a cast iron pipe. The coating method is not particularly limited. For example, it is used as a normal powder coating method such as electrostatic powder coating, negative charging electrostatic coating (corona), friction charging electrostatic coating (tribo), and fluid immersion coating. And the like. The coating is preferably performed so that the dry film thickness is 60 to 200 μm.

【0045】上記鋳鉄管は、一般に、75〜2600m
mφであり、肉圧が10mm以上と厚く、熱容量が大き
いため、焼き付け時の温度を低くすることが省エネルギ
ーの点から重要である。本発明の鋳鉄管外面塗装用エポ
キシ粉体塗料組成物は、例えば、焼き付け温度を160
℃とした場合、2〜4分の短時間で硬化させることがで
きるため、省エネルギーの観点から非常に好ましい。ま
た、鋳鉄管の内面の塗装をエポキシ樹脂粉体塗料等を用
いて行う場合には、内面の塗膜形成時の余熱で外面の塗
膜を硬化させてもよい。この場合には、被塗物温度14
0〜180℃で塗膜が形成されることが好ましい。
The above cast iron tube is generally 75 to 2600 m
mφ, the thickness is as thick as 10 mm or more, and the heat capacity is large. Therefore, it is important from the viewpoint of energy saving to lower the temperature at the time of baking. The epoxy powder coating composition for coating the outer surface of a cast iron pipe of the present invention has, for example, a baking temperature of 160.
When set to ° C., curing can be performed in a short time of 2 to 4 minutes, which is very preferable from the viewpoint of energy saving. When the inner surface of the cast iron pipe is coated using an epoxy resin powder coating or the like, the outer coating film may be hardened by the residual heat at the time of forming the inner coating film. In this case, the object temperature 14
It is preferable that a coating film is formed at 0 to 180 ° C.

【0046】上記鋳鉄管は、ショットブラスト処理等の
塗装前処理が施されたものであってもよい。また必要で
あれば後焼を実施してもよい。後焼の焼き付け条件は、
被塗物温度150〜200℃で5〜20分程度が好まし
い。
The above-mentioned cast iron pipe may have been subjected to a pre-coating treatment such as a shot blast treatment. If necessary, post-baking may be performed. The post-baking conditions are
The temperature is preferably about 5 to 20 minutes at a temperature of 150 to 200 ° C.

【0047】本発明の鋳鉄管外面塗装用エポキシ粉体塗
料組成物が前駆反応されたものである場合、例えば、以
下のようにして、塗膜を形成することが好ましい。20
0℃程度に予め加熱された鋳鉄管の内面を塗装し、塗装
終了後、必要に応じて、内面をマスキングした後、約1
60℃に加熱された鋳鉄管の外面に、前駆反応を行った
本発明の鋳鉄管外面塗装用エポキシ粉体塗料組成物を塗
装し、被塗物温度140〜160℃で塗膜を形成させ
る。
When the epoxy powder coating composition for outer surface coating of a cast iron pipe of the present invention has been subjected to a precursor reaction, it is preferable to form a coating film, for example, as follows. 20
After coating the inner surface of the cast iron tube preheated to about 0 ° C., after the coating is completed, if necessary,
The outer surface of the cast iron pipe heated to 60 ° C. is coated with the epoxy powder coating composition for coating the outer surface of a cast iron pipe of the present invention, which has undergone a precursor reaction, and a coating film is formed at an object temperature of 140 to 160 ° C.

【0048】このようにして鋳鉄管の外面に本発明の鋳
鉄管外面塗装用エポキシ粉体塗料組成物が塗装された外
面塗装鋳鉄管もまた、本発明の一つである。この外面塗
装鋳鉄管は、鋳鉄管外面の塗膜として要求される性能、
例えば、耐食性、耐衝撃性、可撓性等を有する塗膜を外
面に有しており、上下水道、工業用水道、農業用水、ガ
ス用等の配管材として好適である。
An externally coated cast iron pipe in which the outer surface of the cast iron pipe is coated with the epoxy powder coating composition for coating the outer surface of a cast iron pipe of the present invention in this way is also one of the present invention. This exterior painted cast iron pipe has the performance required as a coating film on the outer surface of the cast iron pipe,
For example, it has a coating film having corrosion resistance, impact resistance, flexibility, and the like on its outer surface, and is suitable as a piping material for water and sewage, industrial water, agricultural water, gas, and the like.

【0049】本発明の鋳鉄管外面塗装用エポキシ粉体塗
料組成物は、軟化点が75〜128℃であり、エポキシ
当量が600〜2200g/eqであるビスフェノール
A型エポキシ樹脂(A)を用いているので、密着性、可
撓性及び耐薬品性が非常に良好であり、貯蔵中に粉体塗
料同士の融着が起こりにくく、塗膜形成時には、140
〜180℃の低温で良好な塗膜を形成することができ
る。また、上記硬化剤(B)を用いているので、硬化塗
膜に更に可撓性を付与することができる。
The epoxy powder coating composition for coating the outer surface of a cast iron pipe according to the present invention uses a bisphenol A type epoxy resin (A) having a softening point of 75 to 128 ° C. and an epoxy equivalent of 600 to 2200 g / eq. Therefore, the adhesiveness, flexibility and chemical resistance are very good, the powder coatings are hardly fused to each other during storage.
A good coating film can be formed at a low temperature of 180 ° C. Further, since the curing agent (B) is used, flexibility can be further imparted to the cured coating film.

【0050】更に、本発明の鋳鉄管外面塗装用エポキシ
粉体塗料組成物は、焼セッコウ(D)が、鋳鉄管外面塗
装用エポキシ粉体塗料組成物に対して、2〜50重量%
となるように配合されたものであるので、本発明の鋳鉄
管外面塗装用エポキシ粉体塗料組成物が塗装された鋳鉄
管では、塗膜の損傷部や欠陥部からの塗膜の剥離やフク
レが発生することがない。これは、塗膜の傷やピンホー
ル等の損傷部や欠陥部の近傍に形成されるカソード部位
から鋳鉄管と塗膜との密着性を低下させる水酸化物イオ
ンが発生するが、塗膜中に存在する焼セッコウ(D)
が、この水酸化物イオンを捕捉する働きを有しているた
めであると考えられる。
Further, the epoxy powder coating composition for coating an outer surface of a cast iron pipe according to the present invention is characterized in that calcined gypsum (D) is 2 to 50% by weight based on the epoxy powder coating composition for an outer coating of a cast iron pipe.
Therefore, in a cast iron pipe coated with the epoxy powder coating composition for coating an outer surface of a cast iron pipe of the present invention, peeling of the coating film from a damaged or defective portion of the coating film or blistering occurs. Does not occur. This is because hydroxide ions, which reduce the adhesion between the cast iron pipe and the coating film, are generated from the cathode site formed near the damaged or defective portion such as a scratch or a pinhole in the coating film. Baked gypsum (D)
However, it is considered that this has a function of capturing this hydroxide ion.

【0051】[0051]

【実施例】以下に実施例を掲げて本発明を更に詳しく説
明するが、本発明はこれら実施例のみに限定されるもの
ではない。
The present invention will be described in more detail with reference to the following examples, but the present invention is not limited to these examples.

【0052】実施例1 エポキシ粉体塗料の製造 エピコート1005F(エポキシ当量950〜1050
g/eq、軟化点約107℃、油化シェルエポキシ社
製)100重量部、エピキュア170(フェノール性水
酸基当量286〜400g/eq、軟化点約90℃、油
化シェル社製)34重量部、2MZ(2−メチルイミダ
ゾール、四国化成工業社製)0.7重量部、焼セッコウ
PH−200(丸石石膏社製)20.0重量部、三菱カ
ーボンMA100(カーボンブラック、三菱化学社製)
2.0重量部、アクロナール4F(表面調整剤、BAS
F社製)0.6重量部を、スーパーミキサー(川田製作
所製)を用いて粒状の均一混合物とし、ついで、コニー
ダー(スイスブス社製)を用いてケーシング温度95℃
及び軸温度35℃で通過時間が45秒となるように軸回
転速度を調節して、溶融混合と同時に前駆反応を行わせ
た。冷却後、ACM粉砕機(ホソカワミクロン社製)を
用いて、平均粒径35μmとなるように粉砕し、エポキ
シ粉体塗料(1)を調製した。
Example 1 Production of Epoxy Powder Coating Epicoat 1005F (Epoxy equivalent 950-1050)
g / eq, softening point of about 107 ° C., 100 parts by weight of Yuka Shell Epoxy Co., Ltd .; Epicure 170 (phenolic hydroxyl equivalent 286 to 400 g / eq, softening point of about 90 ° C., of Yuka Shell Co.) 34 parts by weight; 0.7 parts by weight of 2MZ (2-methylimidazole, manufactured by Shikoku Chemicals), 20.0 parts by weight of calcined gypsum PH-200 (manufactured by Marubishi Gypsum), Mitsubishi Carbon MA100 (carbon black, manufactured by Mitsubishi Chemical Corporation)
2.0 parts by weight, Acronal 4F (surface conditioner, BAS
0.6 parts by weight (made by F company) were made into a granular uniform mixture using a super mixer (manufactured by Kawada Seisakusho), and then a casing temperature of 95 ° C. was obtained using a coneder (manufactured by Swissbus).
The shaft rotation speed was adjusted so that the passage time was 45 seconds at a shaft temperature of 35 ° C., and the precursor reaction was performed simultaneously with the melt mixing. After cooling, the mixture was pulverized using an ACM pulverizer (manufactured by Hosokawa Micron Corporation) so as to have an average particle size of 35 μm to prepare an epoxy powder coating material (1).

【0053】実施例2〜8、比較例1〜4 エポキシ粉
体塗料の製造 表1に示した配合組成に従って、実施例1と同様にし
て、エポキシ粉体塗料(2)〜(8)、比較エポキシ粉
体塗料(1)〜(4)を調製した。
Examples 2 to 8, Comparative Examples 1 to 4 Epoxy powder
Production of body paint According to the composition shown in Table 1, in the same manner as in Example 1, epoxy powder paints (2) to (8) and comparative epoxy powder paints (1) to (4) were prepared.

【0054】実施例9 エポキシ粉体塗料の製造 表1に示した配合組成に従って、実施例1と同様にし
て、各成分をスーパーミキサーを用いて粒状の均一混合
物とし、コニーダーを用いて押し出した後、更に、この
溶融混合物を50℃で20時間保温して、ISO 81
30−6の方法での200℃加熱時の塗料のゲルタイム
が15秒となるように熟成させた後、平均粒径が35μ
mとなるうよに粉砕し、エポキシ粉体塗料(9)を調製
した。
Example 9 Production of Epoxy Powder Coating According to the composition shown in Table 1, each component was made into a granular uniform mixture using a super mixer and extruded using a co-kneader in the same manner as in Example 1. Further, the molten mixture is kept at 50 ° C. for 20 hours to obtain an ISO 81
After aging so that the gel time of the coating when heated at 200 ° C. by the method of 30-6 is 15 seconds, the average particle size is 35 μm.
m to obtain an epoxy powder coating (9).

【0055】[0055]

【表1】 [Table 1]

【0056】表1中、エピコート1003Fは、ビスフ
ェノールA型エポキシ樹脂(エポキシ当量700〜80
0g/eq、軟化点約96℃、油化シェルエポキシ社
製)であり、エポトートYD−907は、ビスフェノー
ルA型エポキシ樹脂(エポキシ当量1300〜1700
g/eq、軟化点117〜127℃、東都化成社製)で
あり、TH−4100は、フェノール性硬化剤(フェノ
ール性水酸基当量725g/eq、軟化点約110℃、
東都化成社製)であり、C11Zは、硬化促進剤(2−ウ
ンデシルイミダゾール、四国化成工業社製)である。
In Table 1, Epicoat 1003F is a bisphenol A type epoxy resin (epoxy equivalent of 700 to 80).
0g / eq, softening point of about 96 ° C, manufactured by Yuka Shell Epoxy Co., Ltd.), and Epotote YD-907 is a bisphenol A type epoxy resin (epoxy equivalent of 1300 to 1700).
g / eq, softening point 117-127 ° C, manufactured by Toto Kasei Co., Ltd., and TH-4100 is a phenolic curing agent (phenolic hydroxyl equivalent 725 g / eq, softening point about 110 ° C,
And C 11 Z is a curing accelerator (2-undecylimidazole, manufactured by Shikoku Chemicals Co., Ltd.).

【0057】実施例11〜17、比較例5〜8 エポキ
シ粉体塗料の製造 表2に示した配合組成に従って、実施例1と同様にし
て、エポキシ粉体塗料(11)〜(17)、比較エポキ
シ粉体塗料(5)〜(8)を調製した。なお、ジシアン
ジアミドは、日本カーバイド工業社製のものを使用し
た。
[0057] Examples 11 to 17, Comparative Examples 5 to 8 epoxy
According to the formulations composition shown in preparation Table 2 shea powder coating, in the same manner as in Example 1, an epoxy powder coating (11) to (17) were prepared to compare epoxy powder coating (5) - (8) . The dicyandiamide used was manufactured by Nippon Carbide Industry Co., Ltd.

【0058】実施例18 エポキシ粉体塗料の製造 表2に示した配合組成に従って、実施例9と同様にし
て、エポキシ粉体塗料(18)を調製した。
Example 18 Production of Epoxy Powder Coating According to the composition shown in Table 2, an epoxy powder coating (18) was prepared in the same manner as in Example 9.

【0059】[0059]

【表2】 [Table 2]

【0060】実施例1〜18及び比較例1〜8で得られ
たエポキシ粉体塗料(1)〜(18)及び比較エポキシ
粉体塗料(1)〜(8)を用いて、鋳鉄部材の塗装を行
った。塗装鋳鉄部材の製造 ダクタイル鋳鉄部材(70×150×20mm)にショ
ットブラスト処理を施し、SSPC−SP5(ホワイト
メタル)とした。この処理板を焼き付け炉で、板温が1
70℃になるまで加熱し、焼き付け炉から取り出したダ
クタイル鋳鉄部材に、直ちに、実施例1で得られたエポ
キシ粉体塗料(1)〜(18)及び比較エポキシ粉体塗
料(1)〜(8)を、それぞれ塗装膜厚が100μmと
なるように静電スプレー塗装を行い、25℃の室温で放
置して、硬化塗膜を形成した。なお、ダクタイル鋳鉄部
材の温度が160℃の時点で塗装を開始し、塗装終了時
の温度は、155℃であった。得られた塗装鋳鉄部材に
ついて、以下の評価を行った。なお、耐屈曲性及び水質
試験については、別に試験片を作成して評価を行った。
Coating of cast iron members using the epoxy powder coatings (1) to (18) and comparative epoxy powder coatings (1) to (8) obtained in Examples 1 to 18 and Comparative Examples 1 to 8. Was done. Production of Painted Cast Iron Member A shot blast treatment was applied to a ductile cast iron member (70 × 150 × 20 mm) to obtain SSPC-SP5 (white metal). This processing plate is baked in a baking oven and the plate temperature is 1
The epoxy powder coatings (1) to (18) and the comparative epoxy powder coatings (1) to (8) obtained in Example 1 were immediately heated to 70 ° C. and immediately applied to the ductile cast iron member taken out of the baking furnace. ) Was subjected to electrostatic spray coating so that each coating film thickness was 100 μm, and left at room temperature of 25 ° C. to form a cured coating film. The coating was started when the temperature of the ductile cast iron member was 160 ° C, and the temperature at the end of the coating was 155 ° C. The following evaluation was performed about the obtained painted cast iron member. In addition, about a bending resistance and a water quality test, a test piece was separately prepared and evaluated.

【0061】仕上がり性 塗装ダクタイル鋳鉄部材の塗面を目視により、以下の基
準で評価した。結果を表3及び表4に示した。 ◎:凹凸が少なく平滑 ○:凹凸はあるが平滑 △:かなり凹凸があり、平滑性が劣る ×:凹凸が著しく、平滑性が極めて劣る
[0061] By visually coated surface finish of paint ductile cast iron, and evaluated according to the following criteria. The results are shown in Tables 3 and 4. ◎: Smoothness with little unevenness 平滑: Smoothness with unevenness か な り: Slight unevenness and poor smoothness ×: Extremely uneven and extremely poor smoothness

【0062】耐食性 塗装ダクタイル鋳鉄部材に、素地に達するまでの1本の
ストレート傷(長さ10cm)を入れ、JIS K 5
400 9.1の塩水噴霧試験に従って、500時間後
のカソード剥離幅の最大値を下記の基準で評価した。結
果を表3及び表4に示した。 ◎:カット傷より片側3mm未満 ○:カット傷より片側3mm以上5mm未満 △:カット傷より片側5mm以上10mm未満 ×:カット傷より片側10mm以上
A single straight scratch (length 10 cm) was made on the corrosion-resistant painted ductile cast iron member until it reached the substrate, and the material was subjected to JIS K5
According to the salt spray test of 400 9.1, the maximum value of the cathode peeling width after 500 hours was evaluated according to the following criteria. The results are shown in Tables 3 and 4. :: less than 3 mm on one side from the cut wound ○: 3 mm or more and less than 5 mm on one side from the cut wound Δ: 5 mm or more and less than 10 mm on one side from the cut wound ×: 10 mm or more on one side from the cut wound

【0063】耐衝撃性 塗装ダクタイル鋳鉄部材の塗装面に、20℃でデュポン
式衝撃試験〔1/2インチ(衝撃部)×500g(荷
重)×50cm(高さ)〕を実施し、衝撃部の塗膜状態
を下記の基準で評価した。 ○:衝撃部のみ塗膜破損 △:衝撃部の塗膜破損及び衝撃部をのぞいた部位に塗膜
浮き ×:衝撃部の塗膜破損及び衝撃部周辺に塗膜剥離
Impact Resistant Coating A DuPont type impact test [1/2 inch (impact portion) × 500 g (load) × 50 cm (height)] was performed on the painted surface of the ductile cast iron member at 20 ° C. The state of the coating film was evaluated according to the following criteria. :: Damage of the coating film only at the impacted part △: Damaged coating at the impacted part and floating of the coating on the part except the impacted part ×: Damaged coating at the impacted part and peeling of the coating around the impacted part

【0064】硬化性 メチルエチルケトンを含ませたガーゼを、塗装ダクタイ
ル鋳鉄部材の塗膜に軽くあてて、拭くように10回往復
させた後の塗膜状態を、下記の基準で評価した。結果を
表3及び表4に示した。 ◎:異常なし ○:塗膜に若干の痕跡があるが、艶の消失がない △:塗膜の溶解は認められないが、艶が消失 ×:塗膜が溶解
Gauze containing curable methyl ethyl ketone was lightly applied to the coating film of the painted ductile cast iron member, and the state of the coating film after reciprocating 10 times was evaluated according to the following criteria. The results are shown in Tables 3 and 4. :: No abnormality :: There is a slight trace on the coating film, but there is no loss of gloss. 溶解: No dissolution of the coating film is observed, but the gloss disappears. ×: The coating film is dissolved.

【0065】耐屈曲性 ブリキ板(150×50×0.3mm)を#180ペー
パーを用いて研磨したものを試験片とした。試験片にエ
ポキシ粉体塗料(1)〜(18)、比較エポキシ粉体塗
料(1)〜(8)をそれぞれ膜厚が約100μmとなる
ように塗装し、被塗物温度160℃で10分間焼き付け
た。耐屈曲性試験は、JIS K 5400 8.1
(耐屈曲性)に従って行い、屈曲試験器の心棒の直径1
0mmで実施し、下記の基準で評価した。結果を表3及
び表4に示した。 ○:塗膜に割れ、はがれを認めない ×:塗膜に割れ、はがれが発生
A test piece was prepared by polishing a flex-resistant tin plate (150 × 50 × 0.3 mm) using # 180 paper. Epoxy powder coatings (1) to (18) and comparative epoxy powder coatings (1) to (8) were applied to the test pieces so as to have a film thickness of about 100 μm, respectively. Baked. The bending resistance test was performed according to JIS K 5400 8.1.
(Bending resistance), and the diameter of the mandrel of the bending tester is 1
The measurement was performed at 0 mm and evaluated according to the following criteria. The results are shown in Tables 3 and 4. :: No cracking or peeling was observed in the coating film ×: Cracking or peeling occurred in the coating film

【0066】水質試験 両面が平らな両面すり板ガラス(200×70×2m
m)を試験片とした。試験片にエポキシ粉体塗料(1)
〜(18)、比較エポキシ粉体塗料(1)〜(8)をそ
れぞれ片面120×70mmの広さで両面及び端部に塗
装し、雰囲気温度180℃の乾燥炉で15分間焼き付け
た。試験は、JWWA K−139の方法に従って行
い、下記の基準で評価した。結果を表3及び表4に示し
た。 ○:全項目合格 ×:不合格項目あり
Water quality test Double-sided frosted glass (200 × 70 × 2 m
m) was used as a test piece. Epoxy powder coating on test piece (1)
To (18) and comparative epoxy powder coatings (1) to (8) were applied on both sides and ends in a size of 120 × 70 mm on each side, and baked in a drying oven at an ambient temperature of 180 ° C. for 15 minutes. The test was performed according to the method of JWWA K-139, and evaluated according to the following criteria. The results are shown in Tables 3 and 4. ○: All items passed ×: Some items failed

【0067】[0067]

【表3】 [Table 3]

【0068】[0068]

【表4】 [Table 4]

【0069】[0069]

【発明の効果】本発明の鋳鉄管外面塗装用エポキシ粉体
塗料組成物は、上述の構成よりなり、極めて耐食性に優
れ、鋳鉄管への付着性にも優れており、仕上がり性も良
好であるので、鋳鉄管外面塗装用として非常に好適であ
る。また、本発明の外面塗装鋳鉄管は、上記本発明の鋳
鉄管外面塗装用エポキシ粉体塗料組成物を用いて塗装し
ているので、耐食性、耐衝撃性、可撓性等に優れた塗膜
を鋳鉄管の外表面に形成させることができ、塗膜の損傷
部や欠陥部において、剥離やフクレを生じさせることが
ない外面塗装鋳鉄管を提供することができる。
The epoxy powder coating composition for coating the outer surface of a cast iron pipe according to the present invention has the above-mentioned constitution, is extremely excellent in corrosion resistance, has excellent adhesion to a cast iron pipe, and has excellent finish. Therefore, it is very suitable for coating the outer surface of a cast iron tube. Moreover, since the outer surface coated cast iron pipe of the present invention is coated using the epoxy powder coating composition for outer surface coating of the cast iron tube of the present invention, a coating film having excellent corrosion resistance, impact resistance, flexibility, etc. Can be formed on the outer surface of a cast iron pipe, and an externally coated cast iron pipe that does not cause peeling or blistering at a damaged portion or a defective portion of a coating film can be provided.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI C09D 163/00 C09D 163/00 F16L 58/04 F16L 58/04 // C08G 59/62 C08G 59/62 59/68 59/68 (72)発明者 斉藤 昌彦 大阪市西区北堀江1丁目12番19号 株式会 社栗本鐵工所内 (72)発明者 道浦 吉貞 大阪市西区北堀江1丁目12番19号 株式会 社栗本鐵工所内 (72)発明者 中村 典生 大阪府寝屋川市池田中町19番17号 日本ペ イント株式会社内────────────────────────────────────────────────── ─── Continued on the front page (51) Int.Cl. 6 Identification code FI C09D 163/00 C09D 163/00 F16L 58/04 F16L 58/04 // C08G 59/62 C08G 59/62 59/68 59/68 (72) Inventor Masahiko Saito 1-12-19 Kitahorie, Nishi-ku, Osaka City Inside Kurimoto Iron Works, Ltd. (72) Inventor Norio Nakamura 19-17 Ikedanakacho, Neyagawa-shi, Osaka Inside Nippon Paint Co., Ltd.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 軟化点が75〜128℃であり、エポキ
シ当量が600〜2200g/eqであるビスフェノー
ルA型エポキシ樹脂(A)、下記一般式(1); 【化1】 (式中、mは、1〜4の整数を表す。)で表される化合
物であって、平均フェノール性水酸基当量が200〜8
00g/eqである硬化剤(B)、イミダゾール系硬化
促進剤及びイミダゾリン系硬化促進剤のうち少なくとも
1種の硬化促進剤(C)、並びに、焼セッコウ(D)か
らなる鋳鉄管外面塗装用エポキシ粉体塗料組成物であっ
て、前記硬化剤(B)のフェノール性水酸基の量は、前
記ビスフェノールA型エポキシ樹脂(A)のエポキシ1
当量に対して、0.5〜1.2当量であり、前記硬化促
進剤(C)の配合量は、前記硬化剤(B)の配合量に対
して、0.1〜15.0重量%であり、かつ、前記焼セ
ッコウ(D)の配合量は、鋳鉄管外面塗装用エポキシ粉
体塗料組成物に対して、2〜50重量%となるように配
合されるものであることを特徴とする鋳鉄管外面塗装用
エポキシ粉体塗料組成物。
1. A bisphenol A type epoxy resin (A) having a softening point of 75 to 128 ° C. and an epoxy equivalent of 600 to 2200 g / eq, represented by the following general formula (1): (Wherein, m represents an integer of 1 to 4), wherein the average phenolic hydroxyl equivalent is 200 to 8;
A hardening agent (B) of at least 00 g / eq, at least one of an imidazole-based hardening accelerator and an imidazoline-based hardening accelerator (C), and an epoxy for coating the outer surface of a cast iron pipe comprising calcined gypsum (D) A powder coating composition, wherein the amount of the phenolic hydroxyl group in the curing agent (B) is the same as the amount of the epoxy 1 in the bisphenol A type epoxy resin (A).
The equivalent amount is 0.5 to 1.2 equivalents, and the compounding amount of the curing accelerator (C) is 0.1 to 15.0% by weight based on the compounding amount of the curing agent (B). And the compounding amount of the calcined gypsum (D) is 2 to 50% by weight based on the epoxy powder coating composition for coating the outer surface of a cast iron pipe. Epoxy powder coating composition for exterior coating of cast iron pipes.
【請求項2】 請求項1記載の鋳鉄管外面塗装用エポキ
シ粉体塗料組成物を用いて塗装されたことを特徴とする
外面塗装鋳鉄管。
2. An externally coated cast iron pipe coated with the epoxy powder coating composition for external coating of a cast iron pipe according to claim 1.
JP06819298A 1998-03-18 1998-03-18 Exterior painted cast iron tube Expired - Fee Related JP3572332B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP06819298A JP3572332B2 (en) 1998-03-18 1998-03-18 Exterior painted cast iron tube

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP06819298A JP3572332B2 (en) 1998-03-18 1998-03-18 Exterior painted cast iron tube

Publications (2)

Publication Number Publication Date
JPH11263926A true JPH11263926A (en) 1999-09-28
JP3572332B2 JP3572332B2 (en) 2004-09-29

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ID=13366687

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009035688A (en) * 2007-08-03 2009-02-19 Kurimoto Ltd Powder coating for cast iron pipe and cast iron pipe
CN105065851A (en) * 2015-07-16 2015-11-18 安徽东阳矿业科技有限公司 Preservative treatment method for pipeline
JP6392952B1 (en) * 2017-08-10 2018-09-19 日本ペイント・インダストリアルコ−ティングス株式会社 Powder coating composition

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009035688A (en) * 2007-08-03 2009-02-19 Kurimoto Ltd Powder coating for cast iron pipe and cast iron pipe
CN105065851A (en) * 2015-07-16 2015-11-18 安徽东阳矿业科技有限公司 Preservative treatment method for pipeline
JP6392952B1 (en) * 2017-08-10 2018-09-19 日本ペイント・インダストリアルコ−ティングス株式会社 Powder coating composition
WO2019031285A1 (en) * 2017-08-10 2019-02-14 日本ペイント・インダストリアルコーティングス株式会社 Powder paint composition
JP2019035004A (en) * 2017-08-10 2019-03-07 日本ペイント・インダストリアルコ−ティングス株式会社 Powder coating composition
CN111032799A (en) * 2017-08-10 2020-04-17 日涂工业涂料有限公司 Powder coating composition
US11512221B2 (en) 2017-08-10 2022-11-29 Nippon Paint Industrial Coatings Co., Ltd. Powder paint composition

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