JPH1135882A - Anticorrosion paint composition - Google Patents
Anticorrosion paint compositionInfo
- Publication number
- JPH1135882A JPH1135882A JP19557097A JP19557097A JPH1135882A JP H1135882 A JPH1135882 A JP H1135882A JP 19557097 A JP19557097 A JP 19557097A JP 19557097 A JP19557097 A JP 19557097A JP H1135882 A JPH1135882 A JP H1135882A
- Authority
- JP
- Japan
- Prior art keywords
- coating film
- coating
- epoxy resin
- composition
- flexible epoxy
- 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
- 239000000203 mixture Substances 0.000 title abstract description 8
- 239000003973 paint Substances 0.000 title description 4
- 239000003822 epoxy resin Substances 0.000 claims abstract description 16
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 16
- 229920005989 resin Polymers 0.000 claims abstract description 15
- 239000011347 resin Substances 0.000 claims abstract description 15
- 239000007787 solid Substances 0.000 claims abstract description 11
- 239000008199 coating composition Substances 0.000 claims description 24
- 238000000576 coating method Methods 0.000 abstract description 37
- 239000011248 coating agent Substances 0.000 abstract description 36
- 239000003795 chemical substances by application Substances 0.000 abstract description 6
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 abstract description 6
- IISBACLAFKSPIT-UHFFFAOYSA-N Bisphenol A Natural products C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 abstract description 4
- 239000011230 binding agent Substances 0.000 abstract description 3
- 230000007547 defect Effects 0.000 abstract description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 abstract description 3
- 239000000049 pigment Substances 0.000 abstract description 3
- 235000015112 vegetable and seed oil Nutrition 0.000 abstract description 3
- 239000008158 vegetable oil Substances 0.000 abstract description 3
- 239000004606 Fillers/Extenders Substances 0.000 abstract description 2
- 239000002202 Polyethylene glycol Substances 0.000 abstract description 2
- 238000005336 cracking Methods 0.000 abstract description 2
- 239000003960 organic solvent Substances 0.000 abstract description 2
- 229920001223 polyethylene glycol Polymers 0.000 abstract description 2
- 230000003405 preventing effect Effects 0.000 abstract 2
- 239000000375 suspending agent Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 238000007654 immersion Methods 0.000 description 6
- 150000003839 salts Chemical class 0.000 description 6
- 229910000831 Steel Inorganic materials 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000010959 steel Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 239000013535 sea water Substances 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 239000008096 xylene Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 235000019482 Palm oil Nutrition 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000010775 animal oil Substances 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000010763 heavy fuel oil Substances 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000002540 palm oil Substances 0.000 description 2
- 229920006122 polyamide resin Polymers 0.000 description 2
- 229920000768 polyamine Polymers 0.000 description 2
- 230000002040 relaxant effect Effects 0.000 description 2
- KPAPHODVWOVUJL-UHFFFAOYSA-N 1-benzofuran;1h-indene Chemical compound C1=CC=C2CC=CC2=C1.C1=CC=C2OC=CC2=C1 KPAPHODVWOVUJL-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000010426 asphalt Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 239000011294 coal tar pitch Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- -1 roller coating Substances 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000011269 tar Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は防食塗料組成物に関
し、特に、高粘度のC重油やパーム油等の流動点の高い
動植物油を運搬する運搬船のカーゴタンクの底部の裏面
(バラストタンクの天井面)のように瞬時の温度変化を
受ける箇所に用いるのに適した長期防食性塗膜を形成す
ることのできる防食塗料組成物に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an anticorrosion coating composition, and more particularly to a back surface (a ceiling of a ballast tank) of a cargo tank of a carrier for carrying animal and vegetable oils having a high pour point such as heavy fuel oil C and palm oil having a high viscosity. The present invention relates to an anticorrosion paint composition capable of forming a long-term anticorrosion coating film suitable for use in a place where an instantaneous temperature change occurs, such as surface (2).
【0002】[0002]
【従来の技術】従来、流動点の高い動植物油を運搬する
運搬船のカーゴタンクの底部の裏面となるバラストタン
クの天井面には、通常、タールエポキシ樹脂塗料JIS
2種又は1種相当品が乾燥膜厚200〜250μmで塗
装されている。また、最近は、変性エポキシ樹脂塗料が
乾燥膜厚250〜300μmで塗装されることも多くな
ってきた。2. Description of the Related Art Conventionally, tar epoxy resin coating JIS is usually provided on a ceiling surface of a ballast tank which is a back surface of a bottom portion of a cargo tank of a carrier ship for transporting animal and vegetable oil having a high pour point.
Two or one equivalents are coated with a dry film thickness of 200 to 250 μm. Also, recently, the modified epoxy resin paint is often applied with a dry film thickness of 250 to 300 μm.
【0003】C重油やパーム油等は常温では粘度が高
く、流動性に乏しいため、荷積み及び荷降しの際にはそ
れらの荷物を加熱して粘度を低くし、作業性を良くする
のが通常である。その加熱温度は50〜70℃程度であ
ることが多いが、80℃以上にすることもある。このよ
うな高温物を荷積すると、バラストタンクの天井面(カ
ーゴタンクの底部の裏面)も積荷と同程度の温度に上昇
する。また、荷降し後には、バラストタンクに海水を注
入するが、冬期の海水は冷たく、5℃以下になることも
ある。このバラストタンクへの海水の注入により、タン
クは急冷却される。[0003] Heavy fuel oil or palm oil has a high viscosity at room temperature and has poor fluidity. Therefore, when loading and unloading, it is necessary to heat the luggage to lower the viscosity and improve workability. Is normal. The heating temperature is often about 50 to 70 ° C, but may be 80 ° C or more. When such a high-temperature object is loaded, the temperature of the ceiling surface of the ballast tank (the back surface at the bottom of the cargo tank) also rises to the same level as the load. After unloading, seawater is injected into the ballast tank, but the seawater in winter is cold and may be 5 ° C or less. By injecting seawater into the ballast tank, the tank is rapidly cooled.
【0004】[0004]
【発明が解決しようとする課題】このように、荷積み、
荷降し、バラストタンクへの注水の繰り返しにより、バ
ラストタンクの天井面は80℃から5℃の範囲内での、
時には80℃以上から5℃以下への瞬時の温度変化を受
け、塗膜の伸縮が激しい環境に曝されることになる。そ
のため通常のバラストタンク用塗料を用いて得た塗膜で
は早期にハガレ、ワレ等の塗膜欠陥が生じ、腐食、錆の
発生が生じ易いという問題点があった。本発明は、上記
のような諸問題を解決するものであり、本発明の目的
は、上記のような環境下においても、長期間に亘り防
食、防錆効果を発揮する塗膜を形成することのできる塗
料組成物を提供することにある。Thus, the loading,
By unloading and repeatedly injecting water into the ballast tank, the ceiling surface of the ballast tank is in the range of 80 ° C to 5 ° C.
Occasionally, an instantaneous temperature change from 80 ° C. or more to 5 ° C. or less causes the coating film to be exposed to an environment in which the film is greatly expanded and contracted. Therefore, there is a problem that a coating film obtained by using a usual coating material for ballast tanks causes coating film defects such as peeling and cracking at an early stage, and corrosion and rust easily occur. The present invention is to solve the above-described problems, and an object of the present invention is to form a coating film that exhibits anti-corrosion and anti-rust effects over a long period of time even under the above-described environment. It is to provide a coating composition which can be used.
【0005】[0005]
【課題を解決するための手段】本発明者らは、上記の目
的を達成するために鋭意検討の結果、防食塗料組成物に
おいて、可撓性エポキシ樹脂を特定量で配合し、塗装後
の塗膜のTg値及び伸び率を特定値に限定することによ
り上記目的が達成されることを見いだし、本発明に到達
した。即ち、本発明の防食塗料組成物は、可撓性エポキ
シ樹脂(固形分)が全樹脂固形分の1〜30重量%を占
めており、塗装後の塗膜のTgが50℃以上となり、塗
膜の伸び率が10%以上となることを特徴とする。Means for Solving the Problems As a result of intensive studies to achieve the above object, the present inventors have formulated a specific amount of a flexible epoxy resin in an anticorrosion coating composition, and applied it after coating. The inventors have found that the above objects can be achieved by limiting the Tg value and elongation percentage of the film to specific values, and have reached the present invention. That is, in the anticorrosion coating composition of the present invention, the flexible epoxy resin (solid content) accounts for 1 to 30% by weight of the total resin solids, and the Tg of the coated film after coating becomes 50 ° C. or more, The film is characterized in that the elongation percentage is 10% or more.
【0006】[0006]
【発明の実施の形態】以下に、本発明の実施の形態につ
いて詳細に説明する。本発明の防食塗料組成物で用いる
ことのできる可撓性エポキシ樹脂としては、ポリエチレ
ングリコールグリシジルエーテル型、ポリプロピレング
リコールグリシジルエーテル型、ビスフェノールAアル
キレンオキサイド付加物のグリシジルエーテル型、ビス
フェノールA重合脂肪酸付加物のグリシジルエーテル
型、ダイマー酸ジグリシジルエステル型の各種エポキシ
樹脂、或いは、これらの2種以上の混合物などが代表的
なものとして挙げることができるが、これらに限定され
るものではない。Embodiments of the present invention will be described below in detail. Examples of the flexible epoxy resin that can be used in the anticorrosion coating composition of the present invention include polyethylene glycol glycidyl ether type, polypropylene glycol glycidyl ether type, glycidyl ether type of bisphenol A alkylene oxide adduct, and bisphenol A polymerized fatty acid adduct. Typical examples include various epoxy resins of glycidyl ether type and diglycidyl dimer acid type, and mixtures of two or more of these, but are not limited thereto.
【0007】本発明の防食塗料組成物は、上記の可撓性
エポキシ樹脂を必須成分として含有し、更に、従来公知
の防食塗料組成物に用いられている諸成分を同様の配合
割合で含有する。即ち、本発明の防食塗料組成物は、上
記の可撓性エポキシ樹脂以外に、アミン硬化エポキシ樹
脂、イソシアネート硬化ポリオール樹脂、塩素化樹脂、
クマロンインデン樹脂、塩化ビニル樹脂、キシレン樹
脂、ケトン樹脂、石油樹脂、コールタールピッチや膨潤
炭のような瀝青質、或いは、これらの2種以上の混合物
などの結合剤、キシレン、トルエンなどの芳香族炭化水
素、アルコール、ケトンなどの有機溶剤を含有すること
ができ、更に必要に応じて、酸化チタン、酸化鉄、カー
ボンブラックなどの着色顔料、タルク、炭酸カルシウ
ム、硫酸バリウム、マイカなどの体質顔料、その他、沈
澱防止剤、流れ止め剤、ハジキ防止剤などの各種添加剤
を含有することができる。The anticorrosion coating composition of the present invention contains the above-mentioned flexible epoxy resin as an essential component, and further contains the same components as those used in conventionally known anticorrosion coating compositions. . That is, the anticorrosion coating composition of the present invention, in addition to the flexible epoxy resin, an amine-cured epoxy resin, an isocyanate-cured polyol resin, a chlorinated resin,
Binders such as coumarone indene resin, vinyl chloride resin, xylene resin, ketone resin, petroleum resin, bitumen such as coal tar pitch and swollen charcoal, or a binder such as a mixture of two or more thereof, and aromatics such as xylene and toluene It can contain organic solvents such as aromatic hydrocarbons, alcohols and ketones, and if necessary, coloring pigments such as titanium oxide, iron oxide and carbon black, extenders such as talc, calcium carbonate, barium sulfate and mica In addition, various additives such as an anti-settling agent, an anti-flow agent, and an anti-cissing agent can be contained.
【0008】本発明の防食塗料組成物においては、可撓
性エポキシ樹脂(固形分)が該可撓性エポキシ樹脂を含
めた全樹脂固形分の1〜30重量%、好ましくは3〜2
5重量%を占める。可撓性エポキシ樹脂(固形分)の含
有量が全樹脂固形分の1重量%未満である場合には、本
発明で目的とする効果が不十分になるので好ましくな
い。逆に30重量%を超えると塗膜が十分な物理的強度
を有さなくなって塗膜欠陥を生じる傾向が大きくなるの
で好ましくない。In the anticorrosion coating composition of the present invention, the flexible epoxy resin (solid content) is 1 to 30% by weight, preferably 3 to 2% by weight of the total resin solids including the flexible epoxy resin.
Accounts for 5% by weight. When the content of the flexible epoxy resin (solid content) is less than 1% by weight of the total resin solid content, the effects intended in the present invention become insufficient, which is not preferable. Conversely, if the content exceeds 30% by weight, the coating film does not have sufficient physical strength, and the tendency to cause coating film defects is undesirably increased.
【0009】また、本発明の防食塗料組成物は、塗装後
の塗膜のTgが50℃以上、好ましくは70℃以上とな
り、塗膜の伸び率が10%以上、好ましくは12%以上
となるものである。塗装後の塗膜のTgが50℃未満で
ある場合には、高温環境下において塗膜の劣化が早くな
る傾向があるので好ましくない。また、塗膜の伸び率が
10%未満である場合には、塗膜が瞬時の温度変化によ
る伸縮応力を緩和することが困難となる傾向があるので
好ましくない。The anticorrosion coating composition of the present invention has a Tg of 50 ° C. or more, preferably 70 ° C. or more after coating, and the elongation of the coating is 10% or more, preferably 12% or more. Things. If the Tg of the coating film after coating is less than 50 ° C., the coating film tends to deteriorate quickly in a high-temperature environment, which is not preferable. Further, when the elongation percentage of the coating film is less than 10%, it is not preferable because the coating film tends to have difficulty in relaxing the stretching stress due to an instantaneous temperature change.
【0010】本発明の防食塗料組成物は、鋼材の表面
に、例えばショットブラスト鋼材の表面を脱脂し、乾燥
させて得た鋼材の表面に直接塗装してもよく、又は鋼材
の表面にショッププライマーを塗装し、その上に塗装し
てもよい。本発明の防食塗料組成物は乾燥膜厚200〜
500μm、好ましくは250〜300μmとなるよう
に塗装し、自然乾燥もしくは100℃以下の温度で強制
乾燥させる。本発明の防食塗料組成物を塗装する塗装方
法としては、ハケ塗装、ローラー塗装、エアースプレ
ー、エアレススプレー、静電スプレー等の従来から一般
に実施されている方法がそのまま採用できる。[0010] The anticorrosion coating composition of the present invention may be applied directly to the surface of a steel material, for example, by degreasing and drying the surface of a shot blasted steel material, or by applying a shop primer to the surface of the steel material. May be painted, and then painted thereon. The anticorrosion coating composition of the present invention has a dry film thickness of 200 to
The paint is applied to a thickness of 500 μm, preferably 250 to 300 μm, and is naturally dried or forcibly dried at a temperature of 100 ° C. or less. As a coating method for applying the anticorrosive coating composition of the present invention, conventionally used methods such as brush coating, roller coating, air spray, airless spray, and electrostatic spray can be used as they are.
【0011】[0011]
【実施例】以下に、実施例及び比較例に基づいて本発明
を更に詳細に説明するが、本発明はこれらの実施例によ
って限定されるものではない。後記の表1に示した成分
のうち、硬化剤であるポリアミン樹脂及びポリアミド樹
脂成分以外の全成分を表1に示した量(重量部)比でサ
ンドミルにて2時間混練して各々の配合物を調製した。
そして、塗装直前にそれらの配合物にポリアミン樹脂又
はポリアミド樹脂成分を表1に示した量(重量部)比で
混合して本発明の防食塗料組成物を調製した。The present invention will be described below in more detail with reference to Examples and Comparative Examples, but the present invention is not limited to these Examples. Of the components shown in Table 1 below, all components other than the polyamine resin and the polyamide resin component as the curing agent were kneaded for 2 hours in a sand mill in the amount (parts by weight) ratio shown in Table 1 to obtain each compound. Was prepared.
Then, immediately before coating, a polyamine resin or a polyamide resin component was mixed with the blended components in the amounts (parts by weight) shown in Table 1 to prepare an anticorrosive coating composition of the present invention.
【0012】ショットブラスト鋼材(JIS G 31
01、70×150×3.2mm)の表面をキシレンで
脱脂し、乾燥させた。この鋼材の表面に上記で得た各々
の塗料組成物をエアースプレーにて乾燥膜厚200μm
になるように塗装し、7日間自然乾燥させた。得られた
塗板につき、ヒートサイクル試験、90℃塩水浸漬試験
を下記の方法により行った。Shot blast steel (JIS G 31)
01, 70 × 150 × 3.2 mm) was degreased with xylene and dried. On the surface of this steel material, each coating composition obtained above was dried by air spraying to a dry film thickness of 200 μm.
And dried naturally for 7 days. The obtained coated plate was subjected to a heat cycle test and a 90 ° C. salt water immersion test by the following methods.
【0013】<ヒートサイクル試験>塗膜の表面を10
0℃まで加熱上昇させ、次いで5℃の氷水に漬けた。こ
の操作を10回繰り返した後、濃度3重量%の食塩水を
満たした容器に試験板を浸漬し、60℃に保持し、1週
間静置した。この操作を1サイクルとし、15サイクル
の操作を行った。 <90℃塩水浸漬試験>濃度3重量%の食塩水を満たし
た容器中に試験板を浸漬し、90℃に保持し、4ヶ月間
静置した。<Heat cycle test>
The mixture was heated to 0 ° C. and then immersed in 5 ° C. ice water. After repeating this operation 10 times, the test plate was immersed in a container filled with a 3% by weight saline solution, kept at 60 ° C., and allowed to stand for one week. This operation was defined as one cycle, and the operation was performed for 15 cycles. <90 ° C. Salt Water Immersion Test> The test plate was immersed in a container filled with a 3% by weight saline solution, kept at 90 ° C., and allowed to stand for 4 months.
【0014】ヒートサイクル試験、90℃塩水浸漬試験
の後に塗膜の付着力を測定し、また塗膜外観を観察し
た。更に、これらの試験の前の塗膜の付着力と試験後の
塗膜の付着力から塗膜の付着力低下率を求めた。これら
を下記の表2の評価基準に基づいて評価した。その結果
は下記の表3に示す通りであった。また、それぞれの単
離塗膜の伸び率及びTgを測定し、塗膜性能との関係を
把握した。After the heat cycle test and the 90 ° C. salt water immersion test, the adhesion of the coating film was measured, and the appearance of the coating film was observed. Further, the rate of decrease in the adhesion of the coating film was determined from the adhesion of the coating film before the test and the adhesion of the coating film after the test. These were evaluated based on the evaluation criteria of Table 2 below. The results were as shown in Table 3 below. Further, the elongation percentage and Tg of each isolated coating film were measured, and the relationship with the coating film performance was grasped.
【0015】[0015]
【表1】 [Table 1]
【0016】[0016]
【表2】 [Table 2]
【0017】[0017]
【表3】 [Table 3]
【0018】表3に示す評価結果からも明かなように、
本発明の防食塗料組成物である実施例1及び実施例2の
塗料組成物は優れた防食性及び耐久性を有している。一
方、可撓性エポキシ樹脂の配合量が全樹脂固形分の30
重量%を超える比較例1の塗料組成物は塗膜の物理的強
度が不十分であり、ヒートサイクル試験、90℃塩水浸
漬試験に耐えることができなかった。また、塗膜の伸び
率が10%未満の比較例2の塗料組成物は耐ヒートサイ
クル性が悪く、塗膜の伸び率が10%未満で塗膜のTg
が50℃未満の比較例3の塗料組成物は耐ヒートサイク
ル性及び90℃塩水浸漬の両方共悪く、塗膜のTgが5
0℃未満の比較例4の塗料組成物は90℃塩水浸漬性が
悪い結果となり、好ましくないものであった。As is clear from the evaluation results shown in Table 3,
The coating compositions of Examples 1 and 2, which are the anticorrosion coating compositions of the present invention, have excellent anticorrosion properties and durability. On the other hand, the compounding amount of the flexible epoxy resin is 30% of the total resin solids.
The coating composition of Comparative Example 1 exceeding 10% by weight had insufficient physical strength of the coating film and could not withstand the heat cycle test and the 90 ° C salt water immersion test. Also, the coating composition of Comparative Example 2 in which the elongation percentage of the coating film was less than 10% was poor in heat cycle resistance, and the elongation percentage of the coating film was less than 10% and the Tg of the coating film was lower.
Is less than 50 ° C., both the heat cycle resistance and the 90 ° C. salt water immersion are poor, and the coating film has a Tg of 5
The coating composition of Comparative Example 4 having a temperature of less than 0 ° C. had poor salt water immersion at 90 ° C., which was not preferable.
【0019】[0019]
【発明の効果】本発明の防食塗料組成物は、温度変化に
よる伸縮応力を緩和することができ且つ長期に亘って防
食性を維持できる塗膜を形成することのできる防食塗料
組成物であり、瞬時の温度変化を受ける箇所を塗装する
のに適している。Industrial Applicability The anticorrosion coating composition of the present invention is an anticorrosion coating composition capable of forming a coating film capable of relaxing stretching stress due to temperature change and maintaining corrosion resistance for a long period of time. Suitable for painting places subject to instantaneous temperature changes.
Claims (1)
樹脂(固形分)が全樹脂固形分の1〜30重量%を占め
ており、塗装後の塗膜のTgが50℃以上となり、塗膜
の伸び率が10%以上となることを特徴とする防食塗料
組成物。In the anticorrosion coating composition, the flexible epoxy resin (solid content) accounts for 1 to 30% by weight of the total resin solids. An anticorrosion coating composition having a film elongation of 10% or more.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19557097A JP3441627B2 (en) | 1997-07-22 | 1997-07-22 | Anticorrosion paint composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19557097A JP3441627B2 (en) | 1997-07-22 | 1997-07-22 | Anticorrosion paint composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH1135882A true JPH1135882A (en) | 1999-02-09 |
| JP3441627B2 JP3441627B2 (en) | 2003-09-02 |
Family
ID=16343330
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP19557097A Expired - Fee Related JP3441627B2 (en) | 1997-07-22 | 1997-07-22 | Anticorrosion paint composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3441627B2 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7143677B2 (en) | 2003-05-01 | 2006-12-05 | Helen Of Troy Limited | Food slicer |
| US7172653B2 (en) * | 2002-09-24 | 2007-02-06 | Basf Aktiengesellschaft | Solid pigment preparations comprising surface-active additives based on alkoxylated bisphenols |
-
1997
- 1997-07-22 JP JP19557097A patent/JP3441627B2/en not_active Expired - Fee Related
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7172653B2 (en) * | 2002-09-24 | 2007-02-06 | Basf Aktiengesellschaft | Solid pigment preparations comprising surface-active additives based on alkoxylated bisphenols |
| US7143677B2 (en) | 2003-05-01 | 2006-12-05 | Helen Of Troy Limited | Food slicer |
Also Published As
| Publication number | Publication date |
|---|---|
| JP3441627B2 (en) | 2003-09-02 |
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