JP6810420B2 - Undercoat material and coating film forming method using this - Google Patents
Undercoat material and coating film forming method using this Download PDFInfo
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- JP6810420B2 JP6810420B2 JP2017020537A JP2017020537A JP6810420B2 JP 6810420 B2 JP6810420 B2 JP 6810420B2 JP 2017020537 A JP2017020537 A JP 2017020537A JP 2017020537 A JP2017020537 A JP 2017020537A JP 6810420 B2 JP6810420 B2 JP 6810420B2
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- 239000000463 material Substances 0.000 title claims description 43
- 238000000576 coating method Methods 0.000 title claims description 40
- 239000011248 coating agent Substances 0.000 title claims description 39
- 238000000034 method Methods 0.000 title claims description 16
- PAZHGORSDKKUPI-UHFFFAOYSA-N lithium metasilicate Chemical compound [Li+].[Li+].[O-][Si]([O-])=O PAZHGORSDKKUPI-UHFFFAOYSA-N 0.000 claims description 18
- 229910052912 lithium silicate Inorganic materials 0.000 claims description 18
- 239000000839 emulsion Substances 0.000 claims description 16
- 239000003973 paint Substances 0.000 claims description 13
- 239000003822 epoxy resin Substances 0.000 claims description 11
- 229920000647 polyepoxide Polymers 0.000 claims description 11
- 239000002270 dispersing agent Substances 0.000 claims description 10
- 239000000049 pigment Substances 0.000 claims description 10
- 229920006243 acrylic copolymer Polymers 0.000 claims description 8
- 239000007864 aqueous solution Substances 0.000 claims description 8
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 7
- 229920001577 copolymer Polymers 0.000 claims description 7
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000002184 metal Substances 0.000 claims description 5
- 239000000843 powder Substances 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 35
- 239000002245 particle Substances 0.000 description 13
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 11
- 229910000831 Steel Inorganic materials 0.000 description 11
- 239000010959 steel Substances 0.000 description 11
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 238000012360 testing method Methods 0.000 description 7
- 239000002002 slurry Substances 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 4
- 229910052742 iron Inorganic materials 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000004570 mortar (masonry) Substances 0.000 description 4
- 230000000149 penetrating effect Effects 0.000 description 4
- 230000007423 decrease Effects 0.000 description 3
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- IDNHOWMYUQKKTI-UHFFFAOYSA-M lithium nitrite Chemical compound [Li+].[O-]N=O IDNHOWMYUQKKTI-UHFFFAOYSA-M 0.000 description 2
- 238000013507 mapping Methods 0.000 description 2
- 238000002161 passivation Methods 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 239000000523 sample Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 238000004381 surface treatment Methods 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 1
- 241000221535 Pucciniales Species 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 238000007718 adhesive strength test Methods 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 239000012615 aggregate Substances 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- -1 chlorine ions Chemical class 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 150000002641 lithium Chemical group 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 239000011414 polymer cement Substances 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000005488 sandblasting Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 238000012795 verification Methods 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
- Paints Or Removers (AREA)
Description
本発明は、船倉表面に塗布する下塗り材及びこれを用いた塗膜形成方法に関する。 The present invention relates to an undercoat material to be applied to the surface of a hold and a coating film forming method using the same.
貨物運搬船の船倉表面は、エポキシ樹脂系塗料によって被覆されているが、石炭や鉱石などの積荷その物と積み下ろし時に使用するブルドーザー等の重機の両方から強い衝撃を受けるため、腐食による発錆や摩耗などによる塗膜の劣化が著しい。エポキシ樹脂系塗料に硬度の高いアルミナ粒子などを混合して塗膜の耐用年数を延ばす工夫などもなされてはいるが、未だコストに見合う充分な耐用年数を有する塗膜の開発には至っていない。そのため、1〜3年ごとに船倉表面の塗り替えが行われている。しかし、エポキシ樹脂系塗料の場合、サンドブラストなどによる船倉表面の錆落とし処理が必要となるため、工程数が多く工賃が高いという問題がある。 The surface of the hold of a cargo carrier is covered with epoxy resin paint, but it receives strong impact from both the cargo itself such as coal and ore and heavy machinery such as bulldozers used for loading and unloading, so it rusts and wears due to corrosion. The deterioration of the coating film due to such factors is remarkable. Although efforts have been made to extend the useful life of the coating film by mixing epoxy resin-based paint with highly hard alumina particles, etc., a coating film having a sufficient useful life commensurate with the cost has not yet been developed. Therefore, the surface of the hold is repainted every 1 to 3 years. However, in the case of epoxy resin-based paint, there is a problem that the number of processes is large and the wages are high because it is necessary to remove rust on the surface of the hold by sandblasting or the like.
他方、鉄の防錆方法の一つとして、鉄の表面をアルカリ性に保ち不動態化する方法が知られている。一般に、鉄はpH9〜12.5の範囲においてFe2O3の不動態層が形成され安定な状態になるといわれている。例えば特許文献1には、ポリマーセメントと骨材と水と亜硝酸リチウム溶液とを混合してなるモルタルをモルタル吹付ノズルを介してコンクリート構造体の所定個所に吹き付けることを特徴とするモルタル吹付工法の発明が開示されている。この発明では、コンクリート中に埋設されている鉄材表面の塩素イオンによって破壊された不動態皮膜が亜硝酸リチウムにより再生され錆発生を防止する。 On the other hand, as one of the rust preventive methods for iron, a method for keeping the surface of iron alkaline and passivating it is known. In general, iron is said to be in a stable state by forming a passivation layer of Fe 2 O 3 in the pH range of 9 to 12.5. For example, Patent Document 1 describes a mortar spraying method characterized in that a mortar obtained by mixing polymer cement, aggregate, water, and lithium nitrite solution is sprayed onto a predetermined portion of a concrete structure via a mortar spraying nozzle. The invention is disclosed. In the present invention, the passivation film destroyed by chlorine ions on the surface of the iron material embedded in concrete is regenerated by lithium nitrite to prevent rust formation.
また、特許文献2には、珪酸ソーダと亜鉛粉末とを混合して調整した亜鉛粉末含有スラリーに珪酸リチウムを混合撹拌して得られる水系コーティング材の発明が開示されている。亜鉛粉末含有スラリーは、亜鉛粉末がシリカの緻密な被膜で覆われていて水中安定性に優れており、長時間放置しても品質が変わらない。そのため、亜鉛粉末含有スラリーを用いて水系コーティング材を調整することによって、金属に塗布したときの強い付着性、塗膜の十分な硬さ、耐塩水噴霧性等の優れた防錆性を有する水系コーティング材を得ることができる。 Further, Patent Document 2 discloses an invention of an aqueous coating material obtained by mixing and stirring lithium silicate in a zinc powder-containing slurry prepared by mixing sodium silicate and zinc powder. The zinc powder-containing slurry has excellent stability in water because the zinc powder is covered with a dense film of silica, and the quality does not change even if it is left for a long time. Therefore, by adjusting the water-based coating material using the zinc powder-containing slurry, the water-based coating material has excellent rust prevention properties such as strong adhesion when applied to metal, sufficient hardness of the coating film, and salt spray resistance. A coating material can be obtained.
特許文献1に記載されているモルタルは、長期防錆性に優れているとされているが、船倉表面に塗布する場合、塗膜厚さを700μm〜800μm程度にする必要があり、従来のエポキシ樹脂系塗料の3〜4倍の高コストとなる。
また、特許文献2に記載されている亜鉛粉末含有スラリー及び水系コーティング材は、基本的に、水系ジンクリッチ塗料を、より安価に提供するものである。ジンクリッチ塗料は、素地が露出する塗膜欠陥が発生した際に、鋼がカソード、亜鉛粉末がアノードとして作用することにより鋼を防食する(犠牲防食作用)。従って、鋼材表面を完全にケレンしておかないと、亜鉛粉末の効果が得られないという問題がある。
The mortar described in Patent Document 1 is said to have excellent long-term rust prevention properties, but when applied to the surface of a hold, the coating thickness needs to be about 700 μm to 800 μm, and conventional epoxy is used. The cost is 3 to 4 times higher than that of resin paint.
Further, the zinc powder-containing slurry and the water-based coating material described in Patent Document 2 basically provide a water-based zinc rich paint at a lower cost. Zinc rich paint protects steel by acting as a cathode and zinc powder as an anode when a coating film defect that exposes the substrate occurs (sacrificial anticorrosion action). Therefore, there is a problem that the effect of zinc powder cannot be obtained unless the surface of the steel material is completely cleaned.
本発明はかかる事情に鑑みてなされたもので、塗膜の高強度化と下地処理の軽減によるコストの削減が可能となる下塗り材及びこれを用いた塗膜形成方法を提供することを目的とする。 The present invention has been made in view of such circumstances, and an object of the present invention is to provide an undercoat material capable of increasing the strength of a coating film and reducing the base treatment to reduce costs, and a coating film forming method using the same. To do.
上記目的を達成するため、第1の発明は、船倉表面に塗布する下塗り材であって、
珪酸リチウムを6〜12質量%、アクリル系共重合体エマルジョン又はアクリル/スチレン共重合体エマルジョンを3〜6質量%、顔料を2〜4質量%、分散剤を0.2〜0.4質量%含む水溶液からなることを特徴としている。
In order to achieve the above object, the first invention is an undercoat material to be applied to the surface of a hold.
6-12% by mass of lithium silicate, 3-6% by mass of acrylic copolymer emulsion or acrylic / styrene copolymer emulsion, 2-4% by mass of pigment, 0.2-0.4% by mass of dispersant It is characterized by being composed of a containing aqueous solution.
本発明では、船倉表面に発生した錆粒子の間に下塗り材を浸透させることにより、錆粒子を骨格とする強固な塗膜を形成する。
珪酸リチウムは、水溶液中において、鎖状分子がリチウム原子を取り囲むポリシリケートとして存在する。ポリシリケート構造は、錆層に浸透した後、ナノメータオーダーの厚さを有する固形の連続被膜を錆粒子表面に形成し、錆層全体を強固な組織にする。
但し、珪酸リチウム水溶液が硬化すると、塗膜表面に多数の亀裂が発生することが判明したため、本発明では、アクリル系共重合体エマルジョン又はアクリル/スチレン共重合体エマルジョンを珪酸リチウム水溶液に添加し、亀裂を防止する。
なお、珪酸リチウム水溶液は無色透明であるため、顔料を珪酸リチウム水溶液に添加し、隠ぺい率(塗膜が下地の色を覆い隠す度合)を向上させる。併せて、顔料粒子の凝集を防止するため、分散剤を添加する。
In the present invention, a strong coating film having rust particles as a skeleton is formed by infiltrating the undercoat material between the rust particles generated on the surface of the hold.
Lithium silicate exists in an aqueous solution as a polysilicate in which chain molecules surround a lithium atom. In the polysilicate structure, after penetrating into the rust layer, a solid continuous coating having a thickness on the order of nanometers is formed on the surface of the rust particles, and the entire rust layer has a strong structure.
However, since it was found that a large number of cracks were generated on the surface of the coating film when the aqueous solution of lithium silicate was cured, in the present invention, an acrylic copolymer emulsion or an acrylic / styrene copolymer emulsion was added to the aqueous solution of lithium silicate. Prevent cracks.
Since the lithium silicate aqueous solution is colorless and transparent, a pigment is added to the lithium silicate aqueous solution to improve the hiding rate (the degree to which the coating film covers the underlying color). At the same time, a dispersant is added to prevent agglomeration of pigment particles.
また、第2の発明は、船倉表面に塗膜を形成する方法であって、
船倉表面に4種ケレン相当以上の清浄度となる下地処理を施す工程と、
下地処理された前記船倉表面に、第1の発明に係る下塗り材を塗布して下塗り層を形成する工程と、
前記下塗り層上にエポキシ樹脂塗料を塗布して上塗り層を形成する工程とを備えることを特徴としている。
The second invention is a method of forming a coating film on the surface of a hold.
The process of applying a base treatment to the surface of the hold to make it as clean as 4 types of keren,
A step of applying the undercoat material according to the first invention to form an undercoat layer on the surface of the hold that has been subjected to the base treatment, and
It is characterized by including a step of applying an epoxy resin paint on the undercoat layer to form an overcoat layer.
本発明では、錆層を船倉表面の被膜として利用するため、従来のような入念な下地処理を必要とせず、4種ケレン相当の清浄度でよい。下地追従性及び一定の耐水性が要求される上塗り層には、変形能力が高く耐水性に優れるエポキシ樹脂塗料を使用する。 In the present invention, since the rust layer is used as a film on the surface of the hold, the cleanliness equivalent to that of 4 types of keren is sufficient without the need for the conventional careful surface treatment. An epoxy resin paint with high deformation ability and excellent water resistance is used for the topcoat layer, which requires base followability and a certain level of water resistance.
また、第2の発明に係る塗膜形成方法では、前記エポキシ樹脂塗料は金属粉を含むことを好適とする。これにより、上塗り層の耐摩耗性が向上する。 Further, in the coating film forming method according to the second invention, it is preferable that the epoxy resin coating material contains a metal powder. This improves the wear resistance of the topcoat layer.
本発明では、船倉表面に発生した錆粒子の間に下塗り材を浸透させることにより、錆粒子を骨格とする強固な塗膜を形成するので、高強度の塗膜を実現することができる。また、従来のような入念な下地処理が不要となるので、コストの削減が可能となる。 In the present invention, by infiltrating the undercoat material between the rust particles generated on the surface of the hold, a strong coating film having the rust particles as a skeleton is formed, so that a high-strength coating film can be realized. In addition, since the conventional careful surface treatment is not required, the cost can be reduced.
続いて、添付した図面を参照しつつ、本発明を具体化した実施の形態について説明し、本発明の理解に供する。 Subsequently, an embodiment embodying the present invention will be described with reference to the attached drawings, and the present invention will be understood.
[本発明の技術思想]
本発明では、船倉を構成する鋼材10の表面に発生した錆粒子11の間に下塗り材12を浸透させることにより、錆粒子11を骨格とする強固な塗膜を形成する(図1参照)。具体的には、錆層中の浮き錆等を除去し、鋼材10表面に残存する錆層に、珪酸リチウムを含む下塗り材12を浸透させ、錆層と一体化した下塗り層を形成する。
下塗り材12に含まれる珪酸リチウムは、錆粒子11からなる錆層に浸透した後、ナノメータオーダーの厚さを有する固形の連続被膜を錆粒子表面に形成し、錆層全体を強固な組織にする。
[Technical Idea of the Present Invention]
In the present invention, the undercoat material 12 is infiltrated between the rust particles 11 generated on the surface of the steel material 10 constituting the hold to form a strong coating film having the rust particles 11 as a skeleton (see FIG. 1). Specifically, floating rust and the like in the rust layer are removed, and the undercoat material 12 containing lithium silicate is impregnated into the rust layer remaining on the surface of the steel material 10 to form an undercoat layer integrated with the rust layer.
Lithium silicate contained in the undercoat material 12 penetrates into the rust layer composed of rust particles 11 and then forms a solid continuous film having a thickness on the order of nanometers on the surface of the rust particles to make the entire rust layer a strong structure. ..
鋼材表面に残存する錆層に珪酸リチウムを含む下塗り材を浸透させた試験片断面の元素マッピングを図2に示す。例えば電子線マイクロアナライザ(EPMA)の場合、試料に電子線を照射して発生する特性X線の波長と強度から構成元素を分析することができる。
図2(A)はFe、図2(B)はO、図2(C)はSiの各分布を示している。Feは母材である鋼材を、Oは錆である酸化鉄を、Siは珪酸リチウムの分布を示していると解釈することができ、錆層の深部まで珪酸リチウムが浸透していることが図2からわかる。
FIG. 2 shows an elemental mapping of a cross section of a test piece in which an undercoat material containing lithium silicate is impregnated into a rust layer remaining on the surface of a steel material. For example, in the case of an electron probe microanalyzer (EPMA), constituent elements can be analyzed from the wavelength and intensity of characteristic X-rays generated by irradiating a sample with an electron beam.
2 (A) shows Fe, FIG. 2 (B) shows O, and FIG. 2 (C) shows Si. It can be interpreted that Fe indicates the distribution of steel, which is the base material, O indicates iron oxide, which is rust, and Si indicates the distribution of lithium silicate, and it is shown that lithium silicate has penetrated deep into the rust layer. You can see from 2.
[下塗り材]
本発明に係る下塗り材は、船倉表面に塗布する下塗り材であって、珪酸リチウムを6〜12質量%、アクリル系共重合体エマルジョン又はアクリル/スチレン共重合体エマルジョンを3〜6質量%、顔料を2〜4質量%、分散剤を0.2〜0.4質量%含む水溶液から構成されている。
[Undercoat material]
The undercoat material according to the present invention is an undercoat material to be applied to the surface of the ship's warehouse, and contains 6 to 12% by mass of lithium silicate, 3 to 6% by mass of an acrylic copolymer emulsion or an acrylic / styrene copolymer emulsion, and a pigment. It is composed of an aqueous solution containing 2 to 4% by mass and 0.2 to 0.4% by mass of a dispersant.
珪酸リチウムが12質量%超であると、スラリー濃度が上昇して錆層への浸透力が低下するだけでなく、硬化後の塗膜に亀裂が発生する。一方、珪酸リチウムが6質量%未満であると、錆層への浸透作用が不十分となる。 If the amount of lithium silicate exceeds 12% by mass, not only the slurry concentration increases and the penetrating power into the rust layer decreases, but also cracks occur in the cured coating film. On the other hand, if the amount of lithium silicate is less than 6% by mass, the penetrating action into the rust layer becomes insufficient.
アクリル系共重合体エマルジョン又はアクリル/スチレン共重合体エマルジョンが6質量%超であると、錆層への浸透力が低下する。一方、アクリル系共重合体エマルジョン又はアクリル/スチレン共重合体エマルジョンが3質量%未満であると、所定の柔軟性と付着強度が確保できない。
なお、珪酸リチウムとアクリル系共重合体エマルジョン又はアクリル/スチレン共重合体エマルジョンの質量比は、2:1程度が好ましい。
If the amount of the acrylic copolymer emulsion or the acrylic / styrene copolymer emulsion exceeds 6% by mass, the penetrating power into the rust layer decreases. On the other hand, if the acrylic copolymer emulsion or the acrylic / styrene copolymer emulsion is less than 3% by mass, the predetermined flexibility and adhesion strength cannot be ensured.
The mass ratio of lithium silicate to the acrylic copolymer emulsion or the acrylic / styrene copolymer emulsion is preferably about 2: 1.
顔料には、酸化チタンやアルミニウム・ペーストなどを使用することができる。
顔料が4質量%超であると、錆層への珪酸リチウムの浸透が阻害される。一方、顔料が2質量%未満であると、隠ぺい率が低下する。
As the pigment, titanium oxide, aluminum paste, or the like can be used.
If the amount of the pigment exceeds 4% by mass, the penetration of lithium silicate into the rust layer is inhibited. On the other hand, if the pigment content is less than 2% by mass, the hiding rate decreases.
分散剤には、湿潤分散剤やノニオン系界面活性剤などを使用することができる。
分散剤が0.4質量%超であると、所定の付着強度が得られない。一方、分散剤が0.2質量%未満であると、顔料粒子が凝集する。
As the dispersant, a wet dispersant, a nonionic surfactant, or the like can be used.
If the dispersant is more than 0.4% by mass, the predetermined adhesion strength cannot be obtained. On the other hand, if the dispersant is less than 0.2% by mass, the pigment particles agglomerate.
[上塗り材]
上塗り材には、金属粉を10〜15質量%含有するエポキシ樹脂塗料を使用する。
金属粉としてはアルミナなどを使用することができる。
[Topcoat material]
As the topcoat material, an epoxy resin paint containing 10 to 15% by mass of metal powder is used.
Alumina or the like can be used as the metal powder.
[塗膜形成方法]
塗膜の形成手順を以下に示す。
(STEP−1)
船倉表面に4種ケレン相当以上の清浄度となる下地処理を施す。
4種ケレンは、粉化物及び汚れを落とす程度の下地処理であり、例えば、15MPa〜25MPa程度の水圧の高圧水をノズルから船倉表面に向けて噴射して船倉表面の下地処理を行えばよい。
[Coating film forming method]
The procedure for forming the coating film is shown below.
(STEP-1)
The surface of the hold is subjected to a base treatment that is as clean as 4 types of keren.
Class 4 keren is a base treatment that removes powders and dirt. For example, high-pressure water having a water pressure of about 15 MPa to 25 MPa may be sprayed from a nozzle toward the hold surface to perform a base treatment on the hold surface.
(STEP−2)
下地処理された船倉表面に、前述した下塗り材を塗布して下塗り層を形成する。
下塗り層の厚さは20μm〜40μm程度(塗量として100g/m2程度)とする。
乾燥時間の目安は約1日間であるが、錆層の状況によって変動する。
(STEP-2)
The above-mentioned undercoat material is applied to the surface of the hold that has been subjected to the base treatment to form an undercoat layer.
The thickness of the undercoat layer is about 20 μm to 40 μm (a coating amount of about 100 g / m 2 ).
The standard drying time is about one day, but it varies depending on the condition of the rust layer.
(STEP−3)
下塗り層上に、前述したエポキシ樹脂塗料を塗布して上塗り層を形成する。
上塗り層の厚さは30μm〜60μm程度(塗量として160g/m2〜320g/m2程度)とする。
乾燥時間の目安は約1日間である。
(STEP-3)
The epoxy resin paint described above is applied onto the undercoat layer to form the overcoat layer.
The thickness of the overcoat layer is about 30μm~60μm (160g / m 2 ~320g / m 2 about the coating amount).
The standard drying time is about one day.
以上、本発明の一実施の形態について説明してきたが、本発明は何ら上記した実施の形態に記載の構成に限定されるものではなく、特許請求の範囲に記載されている事項の範囲内で考えられるその他の実施の形態や変形例も含むものである。 Although one embodiment of the present invention has been described above, the present invention is not limited to the configuration described in the above-described embodiment, and is within the scope of the matters described in the claims. It also includes other possible embodiments and variations.
本発明の効果について検証するために実施した検証試験について説明する。
試験に使用した下塗り材の配合を表1に示す。エマルジョンにはアクリル系共重合体エマルジョンを、顔料にはアルミニウム・ペーストを、分散剤には湿潤分散剤を使用した。
The verification test carried out for verifying the effect of the present invention will be described.
Table 1 shows the composition of the undercoat material used in the test. An acrylic copolymer emulsion was used as the emulsion, an aluminum paste was used as the pigment, and a wet dispersant was used as the dispersant.
表1に示す下塗り材を用いて実施した塗膜性能試験結果の一覧を表2に示す。
使用した鋼板は無処理自然暴露錆鋼板(150mm×70mm×3.2mm)と4種ケレン自然暴露錆鋼板(150mm×70mm×3.2mm)の2種類とし、上塗り材にはエポキシ樹脂塗料を使用した。塗装方法は刷毛塗装とし、塗布量は下塗り材100g/m2、上塗り材160g/m2とした。なお、試験片の養生は試験室における気乾養生とした。
付着強度試験は、JIS K5600−5−7「塗料一般試験方法−第5部:塗膜の機械的性質−第7節:付着性(プルオフ法)」に準じて実施した。
Table 2 shows a list of coating film performance test results performed using the undercoat material shown in Table 1.
There are two types of steel sheets used: untreated naturally exposed rust steel sheet (150 mm x 70 mm x 3.2 mm) and 4 types of Keren naturally exposed rust steel sheet (150 mm x 70 mm x 3.2 mm), and epoxy resin paint is used as the topcoat material. did. Coating method and brushing, coating amount of the undercoat material 100 g / m 2, and a top coat material 160 g / m 2. The test piece was cured by air drying in the test room.
The adhesive strength test was carried out according to JIS K5600-5-7 "General paint test method-Part 5: Mechanical properties of coating film-Section 7: Adhesiveness (pull-off method)".
CASE1、5、6は、付着強度が1.0N/mm2未満であったため、評価は×(不可)とした。CASE2は、付着強度が1.0N/mm2以上であったが、塗膜表面に亀裂が認められたため、評価は△(可)とした。
一方、CASE3、4は、付着強度が1.0N/mm2以上で、塗膜表面の亀裂も認められなかった。特に、CASE4は、付着強度が1.5N/mm2以上であった。因って、CASE3の評価を○(良)、CASE4の評価を◎(優良)とした。
Since the adhesive strength of CASE 1, 5 and 6 was less than 1.0 N / mm 2 , the evaluation was set to x (impossible). CASE2 had an adhesion strength of 1.0 N / mm 2 or more, but cracks were observed on the surface of the coating film, so the evaluation was set to Δ (OK).
On the other hand, CASE 3 and 4 had an adhesion strength of 1.0 N / mm 2 or more, and no cracks were observed on the coating film surface. In particular, CASE4 had an adhesion strength of 1.5 N / mm 2 or more. Therefore, the evaluation of CASE3 was evaluated as ◯ (good), and the evaluation of CASE4 was evaluated as ⊚ (excellent).
10:鋼材、11:錆粒子、12:下塗り材 10: Steel material, 11: Rust particles, 12: Undercoat material
Claims (3)
珪酸リチウムを6〜12質量%、アクリル系共重合体エマルジョン又はアクリル/スチレン共重合体エマルジョンを3〜6質量%、顔料を2〜4質量%、分散剤を0.2〜0.4質量%含む水溶液からなることを特徴とする下塗り材。 An undercoat material that is applied to the surface of the hold.
6-12% by mass of lithium silicate, 3-6% by mass of acrylic copolymer emulsion or acrylic / styrene copolymer emulsion, 2-4% by mass of pigment, 0.2-0.4% by mass of dispersant An undercoat material comprising an aqueous solution containing the mixture.
船倉表面に4種ケレン相当以上の清浄度となる下地処理を施す工程と、
下地処理された前記船倉表面に、請求項1記載の下塗り材を塗布して下塗り層を形成する工程と、
前記下塗り層上にエポキシ樹脂塗料を塗布して上塗り層を形成する工程とを備えることを特徴とする塗膜形成方法。 It is a method of forming a coating film on the surface of the hold.
The process of applying a base treatment to the surface of the hold to make it as clean as 4 types of keren,
A step of applying the undercoat material according to claim 1 to the surface of the hold that has been subjected to the base treatment to form an undercoat layer, and
A coating film forming method comprising a step of applying an epoxy resin paint on the undercoat layer to form an overcoat layer.
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