JPWO2018062515A1 - Pre-coated metal plate - Google Patents

Abstract

  This pre-coated metal plate has a plated metal plate, a primer layer formed on the surface of the plated metal plate, and an upper film formed on the surface of the primer layer, and the primer layer comprises a binder resin, EPMA having an area within 1.0 μm in the film thickness direction from the interface between the plated metal plate and the primer layer of the cross section in the film thickness direction of the primer layer, comprising pigment particles containing a vanadium compound and a magnesium compound. When observed by mapping, a region where the detected concentration of vanadium element is less than 0.6% does not continuously exist in a direction perpendicular to the film thickness direction of 2.0 μm or more, and the detected concentration of magnesium element is 3 A region of less than 0.0% does not continuously exist in a direction perpendicular to the film thickness direction by 2.0 μm or more.

Description

The present invention relates to a precoated metal sheet.
This application claims priority on September 30, 2016 based on Japanese Patent Application No. 2016-193436 for which it applied to Japan, and uses the content here.

  For home appliances, building materials, and automobiles, pre-coated metal sheets coated with a colored organic film have been used in place of post-painted products that have been painted after conventional molding. This pre-coated metal plate is a rust-proof steel plate or plated steel plate coated with a colored organic film, and has a beautiful appearance, sufficient workability, and good corrosion resistance have.

  When applying pre-coated metal sheets to air conditioner outdoor units and residential equipment with heavy salt damage, high chemical resistance (acid resistance and alkali resistance) is required in addition to corrosion resistance. In recent years, the level required for acid resistance and alkali resistance has been advanced, and conventional pre-coated metal plates cannot satisfy the demand for higher levels.

For example, Patent Document 1 describes a chromium-free undercoat coating composition that can form a coating film having excellent corrosion resistance on an end face, a scratched surface, and a processed portion of a precoated metal sheet. Patent Document 1 describes that this undercoat coating composition contains various non-chromium rust preventive pigments.
Patent Document 1 describes that this undercoat coating composition is useful for improving the corrosion resistance of a coated metal plate, but does not consider any chemical resistance.

Patent Document 2 describes a coated metal plate having a cured coating film excellent in corrosion resistance of a processed portion and an end surface portion as well as corrosion resistance of a flat portion of the coated metal plate. Moreover, it is described that the coating composition which forms a cured coating film contains various rust preventive pigment mixtures as a component of the non-chromic coating composition.
In Patent Document 2, it is described that this coating composition can form a coating film having excellent corrosion resistance at the processed part and the end face part, but no consideration is given to chemical resistance.

Patent Document 3 describes a plated steel sheet containing aluminum as a main component and having a cured coating film excellent in corrosion resistance of a processed part and end face part such as a coated metal plate. Moreover, it is described that the coating composition which forms this cured coating film contains a vanadium compound, a phosphoric acid metal salt containing magnesium, and a magnesium ion-exchanged silica rust pigment mixture as a rust preventive pigment.
Patent Document 3 describes that a coated metal plate on which a cured coating film based on the coating composition is formed has excellent corrosion resistance, but does not consider chemical resistance at all.

  Patent Document 4 describes a coated steel sheet having a coating film formed by using a coating composition that has excellent corrosion resistance and moisture resistance and hardly causes corrosion on a coating film formation target in a short-term corrosion resistance test. Yes. In addition, vanadium compounds and rust preventive accelerators are described as coating compositions. However, Patent Document 4 does not consider any chemical resistance.

As described above, all of the coating compositions described in Patent Documents 1 to 4 are intended to form a corrosion-resistant coating film, and are not intended to improve chemical resistance. .
As a result of the study by the present inventors, even if the coating film contains a rust-preventive pigment, it is not enough that it has the high resistance required for a pre-coated metal plate applied to an air conditioner outdoor unit or a residential equipment with a heavy salt damage site specification. It was found that chemical properties (acid resistance and alkali resistance) cannot be satisfied.

Japanese Unexamined Patent Publication No. 2012-012497 Japanese Unexamined Patent Publication No. 2012-131907 International Publication No. 2012/086494 Japanese Unexamined Patent Publication No. 2013-67699

As described above, a high degree of chemical resistance is required for a pre-coated metal plate that is assumed to be used in an air conditioner outdoor unit or a residential equipment with a heavy salt damage site specification. However, conventional pre-coated metal plates and pre-coated metal plate coatings have not been studied for chemical resistance for the purpose of improving corrosion resistance.
The present invention has been made in view of the above problems. An object of the present invention is to provide a precoated metal sheet having high chemical resistance in addition to corrosion resistance.

The inventors of the present invention have intensively studied to achieve the above object.
As high chemical resistance, for example, there is no abnormality even if immersed in 5% sulfuric acid for 120 hours as acid resistance, and there is no abnormality even if immersed in 5% aqueous sodium hydroxide solution for 120 hours as alkali resistance. It may be required to satisfy the conditions. However, the present inventors conducted the above chemical resistance test using a precoated steel sheet coated with a conventional general paint. As a result, the acid resistance test took about 50 hours and the alkali resistance test took about 24 hours. When exceeded, the coating film was swollen and the requirements could not be satisfied.
Therefore, in order to investigate the cause, the present inventors performed cross-sectional microscopic observation of the swollen portion at the earliest stage in the acid resistance and alkali resistance tests. As a result, when the precoated metal plate was immersed in either acid or alkali, only a small gap was formed at the interface between the coating film and the plating, and no corrosion was observed in the plating itself. In other words, the starting point of the film swell is thought to be a fine gap that occurs when the chemical penetrates the film and reaches the plating surface (the surface of the plating layer of the plated metal plate) and the outermost layer of the plating dissolves. It is done. For this reason, in order to improve chemical resistance, the structure should be such that the chemical does not easily penetrate the coating film, and the adhesion between the coating film and the plating surface layer should be improved so as not to cause a gap for the chemical to enter. It was suggested that it is effective to form a barrier layer so that the plating surface is hardly dissolved by chemicals.
The present invention has been completed based on the above knowledge, and specifically, is as follows.

(1) The precoat metal plate which concerns on 1 aspect of this invention has a plating metal plate, the primer layer formed in the surface of the said plating metal plate, and the upper film formed in the surface of the said primer layer. The primer layer includes a binder resin and pigment particles containing a vanadium compound and a magnesium compound, and the film thickness direction of the cross section in the film thickness direction of the primer layer from the interface between the plated metal plate and the primer layer When the region within 1.0 μm is observed by EPMA mapping, the region where the vanadium element detection concentration is less than 0.6% does not exist continuously in the direction perpendicular to the film thickness direction by 2.0 μm or more. And the area | region where the detection density | concentration of magnesium element is less than 3.0% does not exist 2.0 micrometers or more continuously in the direction perpendicular | vertical to the said film thickness direction.
(2) In the precoated metal plate according to (1), the primer layer has a thickness of 3 to 15 μm, and the maximum major axis in the thickness direction of the pigment particles is 80% of the thickness of the primer layer. It may be the following.
(3) As for the precoat metal plate as described in said (1) or (2), the said binder resin may also contain isocyanate resin.
(4) In the precoated metal plate according to any one of (1) to (3), the content of the pigment particles is 15 to 70% by mass with respect to the total solid mass of the primer layer. There may be.
(5) The precoated metal sheet according to any one of (1) to (4), wherein the vanadium compound is selected from the group consisting of calcium vanadate, magnesium vanadate, and ammonium metavanadate. And the magnesium compound may be one or more selected from the group consisting of magnesium vanadate, magnesium oxide, magnesium hydroxide, and magnesium phosphate.
(6) The precoated metal plate according to any one of (1) to (5) may further include a chemical conversion treatment film between the plated metal plate and the primer layer.
(7) In the precoated metal plate according to any one of (1) to (6), the plated metal plate may be a Zn-Al-Mg plated steel plate.

  According to the above aspect of the present invention, since the distribution of the vanadium compound and the magnesium compound in the primer layer is controlled so as to be densely present in the lower part of the layer, the concentration of the vanadium compound and the magnesium compound is present in the lower part of the primer layer. As a result, a precoated metal sheet having excellent corrosion resistance and high chemical resistance, in which no thin portion is formed, is obtained.

It is a photograph showing the section of the precoat metal plate of the present invention. It is an example of the EPMA mapping photograph (magnification 6000 times) which shows distribution of the vanadium compound (V) in the primer layer cross section of the precoat metal plate of this invention. It is an example of the EPMA mapping photograph (magnification 6000 times) which shows distribution of the magnesium compound (Mg) in the primer layer cross section of the precoat metal plate of this invention. It is the figure which traced the EPMA mapping photograph (magnification 6000 times) of FIG. 2A. It is the figure which traced the EPMA mapping photograph (magnification 6000 times) of FIG. 2B.

  Hereinafter, a precoated metal plate according to an embodiment of the present invention (hereinafter may be referred to as a precoated metal plate according to the present embodiment) will be described in detail.

The precoat metal plate which concerns on this embodiment has a plating metal plate, the primer layer formed in the surface of the said plating metal plate, and the upper layer film | membrane formed on the surface of the said primer layer.
The primer layer includes a binder resin and pigment particles including a vanadium compound and a magnesium compound.
In the primer layer, when a region within 1.0 μm in the film thickness direction from the interface between the plated metal plate and the primer layer in the cross section in the film thickness direction is observed by EPMA mapping, the vanadium element is detected. The region where the concentration is less than 0.6% does not exist continuously in the direction perpendicular to the film thickness direction by 2.0 μm or more, and the region where the magnesium element detection concentration is less than 3.0% It does not exist continuously for more than 2.0 μm in the direction perpendicular to the thickness direction.
The pre-coated metal plate according to the present embodiment may be coated on both sides of the metal plate with the above-mentioned coating film, or may be coated on only one side, or may be partially coated on the surface, depending on the application. Alternatively, the entire surface may be covered. Chemical resistance and corrosion resistance are excellent in the part covered with the coating film of the metal plate. When the above-described film is formed only on one side, a known film may be formed on the opposite side surface in order to impart minimum corrosion resistance and design properties.

<Plating metal plate>
The plated metal plate used for the pre-coated metal plate (painted metal plate) according to the present embodiment is a metal plate having a plated layer on the surface. Although it does not specifically limit as a constituent metal of a metal plate, For example, aluminum, titanium, zinc, copper, nickel, steel, etc. are applicable. When steel is used, it may be ordinary steel or steel containing an additive element such as chromium, and is not particularly limited.
Further, the type of the plating layer formed on the surface of the metal plate is not particularly limited.
Applicable plating layers include, for example, plating made of any one of zinc, aluminum, cobalt, tin, and nickel, and alloy plating containing these metal elements in addition to other metal elements and non-metal elements. Etc. In particular, as the zinc-based plating layer, for example, plating made of zinc, alloy plating of zinc and at least one of aluminum, cobalt, tin, nickel, iron, chromium, titanium, magnesium, manganese, or other Examples include various zinc-based alloy plating containing metal elements and non-metal elements (for example, quaternary alloy plating of zinc, aluminum, magnesium, and silicon).

  As the aluminum plating layer, plating made of aluminum, or alloy plating of at least one of aluminum and silicon, zinc and magnesium (for example, alloy plating of aluminum and silicon, alloy plating of aluminum and zinc, aluminum and silicon) And ternary alloy plating of magnesium).

  Specific examples of the plated metal plate having a zinc-based alloy plated layer or an aluminum-based plated layer include a hot-dip galvanized steel plate (GI) and a Zn—Al—Mg plated steel plate. It is preferable to use a Zn—Al—Mg plated steel plate as the original plate because corrosion resistance superior to that of the hot dip galvanized steel plate can be obtained. There are various types of Zn-Al-Mg plating containing Zn-6% Al-3% Mg, Zn-11% Al-3% Mg-0.2% Si, a small amount of Ni, etc., depending on the ratio of each component. Although present, a Zn-Al-Mg plated steel sheet having a component ratio of Zn-11% Al-3% Mg-0.2% Si is particularly preferred.

  After these plated metal plates are degreased and washed and subjected to normal surface treatment such as chromate treatment, phosphate treatment, or non-chromate treatment, a primer layer can be formed on the surface. Preferred surface treatments are phosphate treatment and non-chromate treatment.

<Primer layer>
The primer layer formed on the surface of the plated metal plate includes a binder resin and pigment particles containing a vanadium compound and a magnesium compound.
Further, in the primer layer of the precoated metal plate according to the present embodiment, the vanadium compound and the magnesium compound are disposed under the primer layer (region within 1.0 μm in the film thickness direction from the interface between the plated metal plate and the primer layer). ), A region where the detected concentration of vanadium element is less than 0.6% does not exist continuously in a direction perpendicular to the film thickness direction by 2.0 μm or more, and the detected concentration of magnesium element It is necessary that the region of less than 3.0% be distributed so as not to continuously exist in a direction perpendicular to the film thickness direction by 2.0 μm or more.

  As long as it is distributed as described above, the form in which these compounds are added is not particularly limited. That is, the form in which the vanadium compound and the magnesium compound are added to the coating solution for forming the primer layer may be either liquid or solid. However, it is preferable to add it in a solid form, particularly in a particle form. The reason for this is that when these compounds are added as liquids, the solvent evaporates during the drying process of the coating film and the compounds are precipitated to solidify, and as a result, the compounds tend to exist in a fine and uniform state in the coating film. This is because it may be necessary to add more compounds to increase the concentration of the vanadium compound and the magnesium compound in the lower region of the primer layer. More specifically, it is preferable to add pigment particles containing a vanadium compound and a magnesium compound to the coating solution for forming the primer layer.

The water containing an acid or alkali component permeates through the upper layer film and the primer layer formed on the surface of the primer layer, reaches the plating surface, and dissolves the plating surface.
The vanadium compound in the primer layer dissolves in the water containing the infiltrated acid or alkali component, and at that time, vanadate ions are released. This vanadate ion reacts with the metal on the plating surface to generate a salt. This salt forms a dense barrier layer at the interface between the plating and the primer layer, thereby suppressing the invading chemical from eroding the plating surface. For this reason, the vanadium compound is densely present in the lower region of the primer layer, so that a high concentration of vanadate ions can be rapidly formed on the plating surface from the very initial stage where the plating is dissolved by the acid or alkali that has reached the plating surface. A dense barrier layer can be formed.

Examples of vanadium compounds include various vanadates such as calcium vanadate, magnesium vanadate, ammonium metavanadate, potassium vanadate, sodium vanadate, ammonium vanadate, phosphorus vanadate, and pigment particles such as vanadium oxide. be able to. Vanadium pentoxide is preferably not used because it is toxic. These compounds may be contained singly or plurally.
Among these vanadium compounds, calcium vanadate, magnesium vanadate, and / or ammonium metavanadate are preferable because they have a good balance between corrosion resistance and water resistance by having appropriate solubility as a rust preventive pigment. Particularly preferred.

It is preferable that content of the vanadium compound in a primer layer is 3-50 mass% with respect to the total solid content mass of a primer layer. When this content is less than 3% by mass, vanadium element is added to the region within 1.0 μm in the film thickness direction from the lower surface (interface between the plated metal plate and the primer layer) of the primer layer in the film thickness direction cross section. This is not preferable because it cannot be made sufficiently dense and there is a concern that the corrosion resistance and chemical resistance may be lowered.
On the other hand, if the content of the vanadium compound with respect to the total solid content of the primer layer exceeds 50% by mass, the effect of improving the corrosion resistance and chemical resistance is saturated and not economical, and the total content of the pigment is increased. This is not preferable because workability may be reduced. From the viewpoint of ensuring the workability required as a pre-coated metal plate after improving corrosion resistance and chemical resistance, the content of the vanadium compound is 4 to 50% by mass relative to the total solid mass of the primer layer. More preferably, 10-30 mass% is further more preferable.

  The magnesium compound in the primer layer dissolves in the water containing the intruding acid or alkali component, and at this time, magnesium ions are released. This magnesium ion reacts with the plating surface to generate a salt. In an alkaline environment, magnesium hydroxide is simultaneously formed. These salts and / or magnesium hydroxide form a dense barrier layer at the plating-primer layer interface, thereby suppressing the invaded chemical from eroding the plating surface.

Magnesium compounds include various magnesium phosphates such as magnesium vanadate, magnesium oxide, magnesium hydroxide, and magnesium phosphate, magnesium silicate, magnesium carbonate, magnesium chloride, magnesium nitrate, magnesium citrate, magnesium acetate, magnesium formate, etc. Various magnesium salts and pigment particles such as magnesium ion-exchanged silica can be used. These compounds may be contained singly or plurally.
Among these magnesium compounds, magnesium vanadate and magnesium oxide are particularly preferable because they have an appropriate solubility as a rust preventive pigment and have a good balance between corrosion resistance and water resistance.

It is preferable that the quantity of the magnesium compound in a primer layer is 3-50 mass% with respect to the total solid content mass of a primer layer. When the content of magnesium compound relative to the total solid mass of the primer layer is less than 3% by mass, within 1.0 μm in the film thickness direction from the lower surface of the primer layer (the interface between the plated metal plate and the primer layer) This is not preferable because the magnesium element cannot be sufficiently densely present in this region, and there is a concern that the corrosion resistance and chemical resistance may be lowered.
On the other hand, if the content of the magnesium compound with respect to the total solid mass of the primer layer exceeds 50% by mass, the effect of improving the corrosion resistance and chemical resistance is saturated and not economical, and the total content of the pigment is increased. This is not preferable because workability may be reduced. The content of the magnesium compound is more preferably 4 to 50% by mass and even more preferably 10 to 30% by mass from the viewpoint of ensuring the required workability after improving the corrosion resistance and chemical resistance.

The vanadium compound and the magnesium compound both exist in a sufficiently fine state when the average particle diameter is 1.0 μm or less. In this case, the vanadium compound and the magnesium compound uniformly dispersed in the coating solution are moved in the direction of the interface with the plated metal plate in the primer layer in the coating and heating / drying process, and densely positioned adjacent to the plating surface. It is advantageous to exist. Therefore, it is preferable that the average particle diameters of the vanadium compound and the magnesium compound in the primer layer are each in the range of 1.0 μm or less.
When the average particle size in the primer layer is 1.0 μm or less, it is preferable that the average particle size of the pigment particles added to the coating solution is also 1.0 μm or less.

  If the average particle diameter of the pigment particles to be added is less than 0.5 μm, it takes time to classify the pigment, which is not preferable. Therefore, the average particle diameter of the vanadium compound and the magnesium compound contained in the primer layer may be 0.5 μm or more.

The method for measuring the average particle size of the vanadium compound and the magnesium compound contained in the primer layer is as follows.
The target pre-coated metal plate is cut into an appropriate size, embedded in a resin so that the cross section in the plate thickness direction can be seen, the cross section is polished, and then the EPMA mapping analysis of the primer layer of the cross section (polished surface) is performed at a magnification of 6000. (Acceleration voltage 15 kV). V and Mg are selected as detection target elements, and mapping imaging of the presence position and element concentration of each element is performed. Next, SEM images of the same position of the same sample are taken at a magnification of 6000, and all the vanadium compounds and magnesium compounds on the SEM image are specified by collating with the previous EPMA mapping image. On the SEM image, the measurement range is 20 μm in the plane direction of the metal plate, and the particle diameters of all the vanadium compounds and magnesium compounds existing in the primer layer within the range (the longest diameter if not a perfect circle: the longest diameter) are measured. And an average particle diameter is calculated about each of a vanadium compound and a magnesium compound, and let these be the average particle diameter of the vanadium compound and magnesium compound which are contained in a primer layer.
When a plurality of vanadium compounds and magnesium compounds are aggregated, the aggregated compound is regarded as one and the particle size (major axis) is measured.

In the primer layer of the precoated metal sheet according to the present embodiment, it is important to contain a vanadium compound and a magnesium compound at the same time.
When a vanadium compound and a magnesium compound are contained at the same time, vanadate ions released from the vanadium compound react with the metal on the plating surface to form a salt and adsorb to the plating surface, while magnesium ions released from the magnesium compound are absorbed. Magnesium hydroxide is formed on the plating surface, and the barrier property is further strengthened by filling the portion of the plating surface with insufficient vanadium salt coating. As a result, alkali resistance, which is considered to be inferior particularly with Al-containing plating, can be drastically improved. This effect is greater than the sum of the effects obtained when the vanadium compound and the magnesium compound are present alone. That is, the synergistic effect is obtained by containing the vanadium compound and the magnesium compound at the same time, and extremely excellent chemical resistance, particularly very excellent alkali resistance can be obtained.

  As described above, in the precoated metal plate according to this embodiment, the vanadium compound and the magnesium compound are intensively distributed in a region near the plated metal plate in the primer layer, and each has a concentration of a certain level or more. This is very important. That is, within the primer layer, the region within 1.0 μm in the film thickness direction from the lower surface (interface between the plated metal plate and the primer layer) of the primer layer in the film thickness direction cross section is mapped to EPMA (Electron Probe Micro Analyzer). When observed by the above, a region where the detected concentration of vanadium element is less than 0.6% does not exist continuously in a direction perpendicular to the film thickness direction (plane direction) of 2.0 μm or more, and the detected concentration of magnesium element Is less than 3.0 μm in the direction perpendicular to the film thickness direction.

The vanadium compound and the magnesium compound are present as particles in the primer layer, and the concentration of each element is low in a portion where these compounds are sparse, and sufficient corrosion resistance and chemical resistance cannot be obtained. In the region where the concentration of vanadium (detected concentration obtained by EPMA mapping) is less than 0.6%, or the concentration of magnesium element (detected concentration) is less than 3.0%, vanadic acid released from vanadium compounds and magnesium compounds The concentration of ions and magnesium ions is insufficient to ensure chemical resistance and corrosion resistance.
That is, when the region within 1.0 μm in the film thickness direction from the lower surface of the primer layer is observed by EPMA mapping, the region where the detected concentration of vanadium element is less than 0.6% or the detected concentration of magnesium element is 3.0. % Region is present in a plane direction (direction perpendicular to (orthogonal to the film thickness direction) 2.0 μm or more, the portion is a portion where the vanadium compound and the magnesium compound are sparse, Since vanadate ions or magnesium ions are not sufficiently supplied to the plating surface, sufficient corrosion resistance and chemical resistance cannot be obtained. Therefore, in the primer layer of the precoated metal plate according to the present embodiment, in the region within 1.0 μm in the film thickness direction from the lower surface of the primer layer, the region where the detected concentration of vanadium element is less than 0.6%, the magnesium element Any region having a detected concentration of less than 3.0% is controlled so as not to continuously exist in a plane direction (direction perpendicular to the film thickness direction) of 2.0 μm or more.

The method for measuring the vanadium element and magnesium element concentrations by EPMA mapping is as follows.
Cut the target pre-coated metal plate into an appropriate size and embed it in a resin so that the cross section in the plate thickness direction can be seen, polish the cross section, and then perform EPMA mapping analysis of the primer layer in the cross section. Is performed at a magnification of 6000 times (acceleration voltage 15 kV) in a range of 20 μm or more in a direction orthogonal to the direction of the angle. V and Mg are selected as detection target elements, and the location of each element and the element concentration are mapped.
Examples of EPMA mapping photographs (magnification of 6000 times) showing the distribution of vanadium compound and magnesium compound in the primer layer cross section of the precoated metal sheet according to this embodiment are shown in FIGS. 3A and 3B. In FIG. 2A and FIG. 2B, the detected density measured in detail at the interval of 2.0 μm or less in the plane direction is shown together with the density indicated by the mapping color. As shown in FIGS. 2A and 2B, in the primer layer of the precoated metal plate according to this embodiment, the region where the vanadium element detection concentration is less than 0.6% is also the region where the magnesium element detection concentration is less than 3.0%. None of them exist continuously in a plane direction (perpendicular to the film thickness direction) of 2.0 μm or more.

  Vanadium compounds and magnesium compounds, which are the source of each ion, are plated due to the concentrated distribution of fine particles of vanadium compounds and magnesium compounds in the region within 1.0 μm from the lower surface of the primer layer cross section. It will be in close proximity. In this case, both vanadate ions and magnesium ions released from these compounds can quickly reach the plating surface. As a result, when a chemical enters, before the plating surface is invaded by the infiltrated chemical, a dense barrier layer is quickly formed on the plating surface to prevent the invading chemical from eroding the plating surface. Can do. As a result, very excellent chemical resistance can be imparted to the precoated metal sheet. Vanadium compounds and magnesium compounds existing in the upper region of the primer layer are also dissolved in water containing acid or alkali components, and vanadate ions and magnesium ions are released. However, when the distance from the plating surface is far, most of the released vanadate and magnesium ions diffuse into the primer layer, and the concentration reaching the plating surface is very small. It is considered very small.

  In addition to improving chemical resistance, corrosion resistance is further improved by intensively distributing fine particles of the vanadium compound and magnesium compound in a region within 1.0 μm from the lower surface of the primer layer cross section. This is demonstrated by the results of the examples described later. The reason for this is not clear, but even when the upper layer film and the primer layer are scratched and the plating surface is damaged, it is concentrated in a region within 1.0 μm from the lower surface of the primer layer cross section. This is considered to be because vanadate ions and magnesium ions released from vanadium compounds and magnesium compounds present immediately cover the damaged plating surface.

  The primer layer of the precoated metal plate according to the present embodiment may include a rust preventive pigment other than the vanadium compound and the magnesium compound described above. For example, rust preventive pigments such as aluminum tripolyphosphate, calcium ion exchange silica, and silica can be used. Moreover, you may further contain extender pigments, such as sedimentation barium sulfate and a clay, and coloring pigments, such as a titanium oxide, as needed.

  The total content of pigment particles (pigment particles that are vanadium compounds, pigment particles that are magnesium compounds, and other pigment particles) is 15 to 70% by mass with respect to the total solid mass of the primer layer. preferable. When the content is less than 15% by mass, the rigidity and cohesive strength of the coating film are reduced, so that the coating film is peeled off when the coating film surface is rubbed with the mold during the press working of the steel sheet (coating film This is not preferable because it is easy to beat. Moreover, since workability will fall when total content exceeds 70 mass%, it is unpreferable. 20-50 mass% is more preferable from a viewpoint of the balance of corrosion resistance, chemical resistance, and workability.

  The size of the pigment particles in the primer layer is preferably such that the maximum major axis in the film thickness direction of all pigment particles is 80% or less of the film thickness of the primer layer. It is considered that the chemical easily enters along the interface between the pigment and the binder resin. Therefore, if there is a pigment with a large major axis exceeding 80% of the primer layer thickness in the film thickness direction, it may become a form close to the pigment penetrating the primer layer up and down, and the penetration of chemicals locally accelerates. There is a risk of being. In this case, it is considered that the position where the chemical has entered becomes the starting point of swelling and the chemical resistance is lowered. From this viewpoint, it is more preferable that the maximum major axis in the film thickness direction of the pigment particles is 60% or less of the film thickness of the primer layer.

The maximum major axis in the film thickness direction of the pigment in the primer layer can be determined by the following method.
The target pre-coated steel sheet is cut into an appropriate size, embedded in a resin so that the cross section in the thickness direction can be seen, the cross section is polished, and then an SEM image of the primer layer in the cross section is taken at a magnification of 6000 times. On the SEM image, the measurement range is 100 μm in the plane direction of the steel sheet, and among all the pigments existing within the measurement range, the particle size in the film thickness direction of the primer layer (if the pigment is not a perfect circle, the pigment occupies The particle diameter in the film thickness direction of the pigment having the largest (distance from the closest position to the far position from the substrate in the range) is defined as the maximum major axis of all the pigments contained in the primer layer. When a plurality of pigments are aggregated, this is regarded as one and the maximum major axis is measured.

  The thickness of the primer layer is preferably 3 to 15 μm. A film thickness of less than 3 μm is not preferable because sufficient corrosion resistance and chemical resistance cannot be obtained. On the other hand, if the film thickness exceeds 15 μm, the workability deteriorates, which is not preferable. From the viewpoint of a good balance of corrosion resistance, chemical resistance, and workability, the thickness of the primer layer is more preferably in the range of 4 to 10 μm.

The binder resin contained in the primer layer is not particularly limited. For example, film-forming resin components such as polymer polyester resin, polyester resin, acrylic resin, epoxy resin, urethane resin, fluorine resin, or modified resins thereof, butylated melamine resin, methylated melamine resin, butylmethyl mixed melamine resin Further, it is possible to use a resin crosslinked by heating with a urea resin, an isocyanate resin, or a mixed crosslinking agent component thereof. Alternatively, an electron beam curable resin, an ultraviolet curable resin, or the like may be used. As the crosslinking agent used for these binder resins, it is particularly preferable to use a curing agent for isocyanate resins. For example, it is preferable to use a film-forming resin component made of a polyester resin that is crosslinked by heating with a crosslinking agent component of an isocyanate resin. The coating film formed by isocyanate curing has the effect of improving the adhesion to the plated metal plate by reacting with the hydroxyl group (—OH) present on the plated surface of the plated metal plate while the crosslinking point becomes a dense urethane bond. This is because a resin having good chemical resistance can be obtained.
As a method for confirming that the binder resin is isocyanate-cured, the target pre-coated metal plate is cut to an appropriate size, embedded in the resin, the cross-sectional direction is polished, and then the primer layer film of the cross-section is microscopically FTed. It can be judged by performing IR measurement by a method such as -IR and confirming the absorption of urethane bonds around 1550 cm ^-1 and the C = N absorption peak derived from isocyanate appearing around 2260 cm ^-1 .

  As isocyanate resins used as curing agents, IPDI (isophorone diisocyanate), TDI (tolylene diisocyanate), MDI (4,4'-diphenylmethane diisocyanate), HMDI (hexamethylene diisocyanate), hydrogenated MDI, hydrogenated XDI (xylylene) Diisocyanates), dimers, dimers, trimers of various isocyanates typified by hydrogenated TDI, etc., and prepolymers having these isocyanates in the skeleton as methanol, ethanol, butanol, propanol, phenol, cresol Chlorophenol, nitrophenol, hydrophenol, acetylacetone, ethyl acetoacetate, ethyl malonate, lactam, phosgene, 1-chloro-2propanol, MEK oximes and the like Those blocks are mentioned click agent. However, the type of isocyanate resin and the type of blocking agent are not limited to those described above. Lactam block MDI and MEK oxime block IPDI are particularly preferred.

  The primer layer of the pre-coated metal plate according to this embodiment may contain additives such as a colorant, a viscosity modifier, a leveling agent, an antifoaming agent, and an ultraviolet absorber in addition to the rust preventive pigment, extender pigment, and binder resin. .

<Upper layer film>
In the precoat metal plate which concerns on this embodiment, it has an upper film | membrane on a primer layer. The upper layer film is not particularly limited as long as it contains a binder resin and a color pigment according to the application. The upper layer film may be a single-layer or multi-layer film as with the upper layer film of a normal precoated steel sheet.

  The binder resin for the upper film is not particularly limited. For example, film-forming resin components such as polymer polyester resin, polyester resin, acrylic resin, epoxy resin, urethane resin, fluorine resin, or modified resins thereof, butylated melamine resin, methylated melamine resin, butylmethyl mixed melamine resin Further, it is possible to use a resin crosslinked by heating with a urea resin, an isocyanate resin, or a mixed crosslinking agent component thereof. Alternatively, an electron beam curable resin, an ultraviolet curable resin, or the like may be used. These resins may be used alone or in combination of two or more.

  As the coloring pigment for the upper layer film, known inorganic and organic coloring pigments can be used. As the inorganic coloring pigment, titanium oxide, zinc oxide, zirconium oxide, calcium carbonate, barium sulfate, alumina, kaolin clay, carbon black, oxidation Iron or the like can be used, and as the organic coloring pigment, Hansa Yellow, pyrazolone orange, phthalocyanine, azo pigment, or the like can be used.

  The thickness of the upper film is preferably 5 to 50 μm as a dry film thickness. If it is less than 5 μm, not only is the chemical resistance and the corrosion resistance lowered, but the color concealment property is lowered and the design property cannot be sufficiently obtained. On the other hand, when the dry film thickness exceeds 50 μm, workability deteriorates. The thickness of the upper film is more preferably 10 to 25 μm.

  The pre-coated metal plate according to the present embodiment can obtain the effect as long as it has the above-described configuration regardless of the manufacturing method. However, for example, a production method including the following steps is preferable because it can be obtained stably.

<Primer layer formation process>
If necessary, a chemical conversion treatment is performed on the plated metal plate by a known method to form a chemical conversion coating, and then a primer layer forming coating solution is applied and dried by heating to form a primer layer.
As the chemical conversion treatment, known non-chromate type treatments can be widely used. In particular, a treatment liquid containing tannic acid and a silane coupling agent is applied and dried so that the dry film weight is 10 to 1000 mg / m ² . This is preferable because extremely high film adhesion can be obtained.

[Coating liquid for primer layer formation]
The coating liquid for forming the primer layer preferably comprises a solvent, the binder resin component described above, and a pigment containing a vanadium compound and a magnesium compound. In addition to these components, additives such as a leveling agent, an antifoaming agent, a colorant, a viscosity modifier, and an ultraviolet absorber may be included.

As described above, in order to detect vanadium element and magnesium element densely from the lower area of the primer layer (area within 1.0 μm in the film thickness direction from the interface between the plated metal plate and the primer layer) In the process where the coating solution for forming the primer layer is applied to the surface of the plated metal plate and then heated and dried, the pigment particles of the vanadium compound and magnesium compound in the coating solution are moved in the direction of the interface with the plated metal plate. Thus, it is effective to localize the vanadium compound and the magnesium compound. The pigment particles containing the vanadium compound and the magnesium compound are both inorganic pigments, and the surface energy thereof is sufficiently higher than that of the binder resin. Therefore, by controlling the pigment particles so that they can move freely in the coating solution, the binder resin component with a relatively low surface tension moves in the direction of the surface of the primer layer due to convection in a series of steps. The pigment particles are localized in the lower region of the primer layer.
In order to make the above-mentioned pigment particles move sufficiently freely in the coating solution, the viscosity of the coating solution for forming the primer layer is set within a range of 20 seconds to 50 seconds with an Iwata cup viscometer. It is desirable. The viscosity of the coating solution can be adjusted by the amount of solvent added. When the viscosity of the coating solution is higher than 50 seconds, the pigment particles containing the vanadium compound and the magnesium compound in the coating solution cannot freely move, and as a result, from the lower region in the primer layer after drying. Vanadium and magnesium elements are not densely detected. On the other hand, when the viscosity of the coating solution is lower than 20 seconds, the solvent ratio in the coating solution is too high, and a coating defect in which bubbles remain in the coating called so-called “waki” occurs in the drying process. It is not preferable as a condition.

  Although the coating method of the coating liquid controlled to the above-mentioned concentration range is not particularly limited, the dipping method, curtain flow method, roll coating method, bar coating method, electrostatic method, brush coating method, T-die method, laminating method, etc. Any method can be used. As a drying method of the coating liquid, high-frequency induction heating that can actively generate convection in the coating liquid by heating from the original plate side in the heating step and promote localization of the vanadium compound pigment and the magnesium compound pigment, or A heating method that combines high-frequency induction heating is desirable.

<Formation process of upper film>
An upper layer coating solution is applied to the plated metal plate on which the primer layer is formed, and then heated and dried to form an upper layer coating. When there are a plurality of upper layer films, this process is further repeated to produce a precoated metal sheet. There are no particular restrictions on the method for applying the upper layer film, and examples include immersion method, curtain flow method, roll coating method, bar coating method, electrostatic method, brush coating method, T-die method, laminating method, and spraying method. Can be mentioned. Also, a wet-on-wet coating method or a multilayer simultaneous coating method can be used.

  As a drying method, any method such as hot air, near infrared rays, far infrared rays, high frequency induction heating, or a heating method using a combination thereof can be applied.

Hereinafter, the present invention will be described using examples. The conditions in the examples are one condition example adopted to confirm the feasibility and effects of the present invention, and the present invention is not limited to this one condition example. The present invention can adopt various conditions as long as the object of the present invention is achieved without departing from the gist of the present invention.
The contents of the plated metal plate, the primer layer, and the upper layer film used in Examples (Examples of the present invention) and Comparative Examples are shown in Tables 1 to 4 and below.

<Plating metal plate>
SD: Zn-11% Al-3% Mg-0.2% Si alloy-plated steel sheet (plate thickness: 0.6 mm, plating adhesion: 40 g / m ² per side)
GI: Hot-dip galvanized steel sheet (plate thickness: 0.6 mm, plating coverage: 40 g / m ² per side)
After alkali degreasing the front and back surfaces of these original plates, after chemical conversion treatment (adhesion amount: 100 mg / m ^{2 on} one side) with a chromate-free chemical conversion treatment solution (a silane coupling agent, tannic acid, silica, and polyester resin mixed system) used. The plating layer was formed on both surfaces of the metal plate.

<Primer layer>
A primer layer was formed on one side of the chemically treated plated metal plate. The film-forming resin component and the curing agent used for the binder resin of the primer layer used in Examples and Comparative Examples are as follows.

(Film-forming resin component)
Polyester resin “Byron 300” (Toyobo Co., Ltd .; Tg 7 ° C., number average molecular weight 26000, hydroxyl value 4, acid value 2 or less)

(Curing agent)
Melamine resin “Cymel 235” (Mitsui Chemicals Co., Ltd .; methoxy / butoxy mixed modified melamine resin)
・ Isocyanate “Coronate 2536” (manufactured by Nippon Polyurethane Industry Co., Ltd .; lactam block / methylene diisocyanate (MDI))
The mixing ratio of the film-forming resin component and the curing agent was 80 to 20 when the curing agent was a melamine resin, and 90 to 10 when the curing agent was an isocyanate (both solid content weight ratio).

The vanadium compound pigment, the magnesium compound pigment, and other rust preventive pigments used in the primer layers used in Examples and Comparative Examples are as follows.
A: Calcium vanadate B: Magnesium vanadate C: Calcium vanadate-magnesium D: Magnesium oxide E: Ca ion exchange silica (Grace, Inc .: Shieldex C303)
F: Aluminum phosphate (manufactured by Teika: K-White # 82)
In Table 1, the pigment concentration shown in italics indicates that the pigment having a particle size of less than 1.0 μm was removed and used.

Further, the following pigment was added to some primer layers in the following addition amount (solid content weight%).
G: Barium sulfate (manufactured by Sakai Chemical Industry Co., Ltd .: precipitated barium sulfate 100) 5%
H: Titanium oxide (Ishihara Sangyo Co., Ltd .: CR95) 2%

  Various binder resins and pigments described above were selected and mixed and dispersed at the pigment weight concentration (PWC) and composition ratio as shown in Table 1 to prepare a primer layer forming coating solution. Thereafter, a one-to-one mixed solvent of cyclohexanone and Solvesso 150 (hydrocarbon organic solvent) was added and diluted to adjust to a predetermined paint viscosity.

  The various primer layer forming coating solutions prepared were applied to the surface of the metal plate that had been subjected to chemical conversion treatment with a bar coater to achieve various dry film thicknesses, and reached a PMT (arrival plate temperature) of 215 ° C in 45 seconds. And dried in a high frequency induction heating oven.

<Upper layer film>
After forming the primer layer, various white paints for pre-coating (polymer polyester / butylated melamine curable FLC7000 paint (Nitrogen white pigment containing 50% by mass in solid content concentration) manufactured by Nippon Paint Co., Ltd.) The film was applied with a bar coater so as to have a dry film thickness, and was dried in a hot air oven under the condition of reaching PMT (reach plate temperature) 230 ° C. in 45 seconds.

<Back film layer>
Common to all examples and comparative examples, the dry film thickness is 5 μm on the back surface (surface on which the primer layer is not formed) of the metal plate subjected to the chemical conversion treatment with the precoat back surface coating material (RB02 coating material manufactured by BASF). Then, it was coated with a bar coater and dried in a hot air oven under the condition that it reached PMT (reaching plate temperature) 230 ° C. in 45 seconds.

<Continuous detectability of vanadium and magnesium elements in the vicinity of plating>
The precoated metal plates of Examples and Comparative Examples prepared as described above were cut into a size of 15 × 20 mm, embedded in resin so that the plate thickness direction could be seen, the cross section was polished, and then the EPMA of the cross section primer layer Mapping analysis was performed at a magnification of 6000 (acceleration voltage 15 kV). In the region within 1.0 μm in the film thickness direction from the lower surface of the primer layer cross section, in the range of 20 μm in the plane direction (direction orthogonal to the film thickness), the region where the detected concentration of vanadium element is less than 0.6% In addition, it was confirmed whether or not a region where the detected concentration of magnesium element was less than 3.0% was continuously present in the plane direction by 2.0 μm or more.

  When the detection concentration of the vanadium element is less than 0.6% and the detection concentration of the magnesium element is less than 3.0%, when there is not continuously 2.0 μm or more in the plane direction (detected densely) Case) was evaluated as OK, and a case where 2.0 μm or more existed continuously in the plane direction (when detection was sparse) was evaluated as NG.

  By the method described above, the average particle diameter of the vanadium compound and the magnesium compound in the primer layer and the maximum major axis in the film thickness direction of the previous pigment were determined.

<Performance evaluation test>
Using the precoated metal plates of Examples and Comparative Examples, the corrosion resistance (SST), chemical resistance (acid resistance, alkali resistance), and workability (T-bending) were evaluated. The test and evaluation methods are shown below.

Corrosion resistance (Salt spray test (SST))
A test piece in which a 70 × 150 mm sample was taken from a pre-coated metal plate, the cut end surface of this sample was painted and sealed, and a deep scratch until reaching the iron ground with a cutter knife was put on the coating film on the steel plate surface; A test piece was prepared by painting and sealing the upper and lower short sides and cutting with a shear so that the two long sides on the left and right face the burr on the back side. About these test pieces, the salt spray test was implemented by the method of JISK5600-7-1 for 960 hours and 1500 hours.

After completion of the salt spray test, the maximum swollen width from the X-cut portion and the cut end surface portion (X cut portion on one side) was measured by magnifying observation. The evaluation criteria were as follows, and 1 was rejected.
4: Less than 2 mm 3: 2 mm or more and less than 4 mm 2: 4 mm or more and less than 6 mm 1: 6 mm or more

Chemical resistance (acid resistance and alkali resistance)
A test piece in which the cut end face and back face of a pre-coated metal plate having a sample size of 50 × 50 mm were sealed with a Teflon (registered trademark) adhesive tape was used in 5% sulfuric acid for 120 hours as an acid resistance test, and 5% sodium hydroxide as an alkali resistance test. It was immersed in an aqueous solution for 120 hours. After the test was completed, the degree of swelling of the coating film was evaluated.

The evaluation criteria were as follows, and 1 was rejected.
4: No swelling at all 3: Mild swelling (blowing area ratio less than 1%)
2: Medium swelling (blowing area ratio of less than 1 to 10%)
1: Severe swelling (bulging area rate of 10% or more)

Workability (T-bending)
A T-bend test was performed. 0T bending was performed at 20 ° C., and the state of cracks and delamination in the processed part was observed with a 10-fold loupe and evaluated as follows, with 1 being rejected.
4: No cracks or peeling.
3: Extremely slight cracking or peeling is observed.
2: A moderate crack or peeling is seen.
1: Severe cracking or peeling is observed.

The evaluation results are shown in Tables 3 and 4. Differences in main evaluation results between the examples and comparative examples will be described.
In Comparative Examples 1, 2, 3, 4, 6, and 7, the pigment particles do not contain either the vanadium compound, the magnesium compound, or both. Therefore, a region with a vanadium element detection concentration of less than 0.6% does not continuously exist in the plane direction of 2.0 μm or more in the region within 1.0 μm in the film thickness direction from the lower surface of the cross section of the primer layer, and In addition, the condition that a region having a detected concentration of magnesium element of less than 3.0% does not continuously exist in a plane direction of 2.0 μm or more was not satisfied. As a result, chemical resistance, particularly alkali resistance, decreased. The corrosion resistance was also low.
The region where the vanadium element detection concentration is less than 0.6% does not continuously exist in the plane direction of 2.0 μm or more, and the region where the magnesium element detection concentration is less than 3.0% continues in the plane direction of 2.0 μm or more. The fact that there is no region where the detection concentration of vanadium element is 0.6% or more exists at intervals of 2.0 μm or less and the region where the detection concentration of magnesium element is 3.0% or more is present throughout the measurement range. It means that it exists at intervals of 2.0 μm or less.

  Comparative Example 5 contained both the vanadium compound and the magnesium compound, but the content was small. As a result, a region with a vanadium element detection concentration of less than 0.6% does not continuously exist in the plane direction of 2.0 μm or more in the region within 1.0 μm in the film thickness direction from the lower surface of the primer layer cross section. In addition, the condition that a region having a detected concentration of magnesium element of less than 3.0% does not continuously exist in the plane direction of 2.0 μm or more was not satisfied. As a result, the chemical resistance, particularly the alkali resistance, was poor, and the corrosion resistance was also low.

  In Comparative Examples 8, 9, and 10, as a result of using the pigment from which the particle diameter of vanadium compound and magnesium compound was less than 1.0 μm was used, the average particle diameter of the contained magnesium compound was increased. As a result, the region where the vanadium element detection concentration is less than 0.6% does not continuously exist in the plane direction of 2.0 μm or more and the region where the magnesium element detection concentration is less than 3.0% is 2.0 μm or more in the plane direction. The condition that it does not exist continuously was not satisfied, and the chemical resistance, particularly alkali resistance, was low.

  In Comparative Example 11, due to the high viscosity of the primer layer forming coating solution, the pigment did not flow sufficiently in the coating and drying steps. As a result, the region where the vanadium element detection concentration is less than 0.6% does not continuously exist in the plane direction of 2.0 μm or more and the region where the magnesium element detection concentration is less than 3.0% is 2.0 μm or more in the plane direction. The condition that it does not exist continuously was not satisfied. Therefore, chemical resistance, especially alkali resistance, was low.

  In each of Examples 1 to 42, corrosion resistance, chemical resistance, and workability were all good. However, there were differences in performance depending on various conditions. For example, Example 15 has a high total pigment concentration in the primer layer, and Examples 17 and 18 have a high pigment concentration in the vanadium compound or magnesium compound, resulting in a high total pigment concentration in the primer layer. There was a tendency for workability to decrease.

  In Example 21, there was a tendency for the workability to decrease due to the thick primer film thickness. In Examples 23 and 24, since the primer film thickness was small, the condition that the major axis of the pigment particles was 80% or less of the film thickness of the primer layer was not satisfied, and the corrosion resistance and chemical resistance tended to decrease. .

  In Example 25, the coating layer has low coating viscosity due to the low viscosity of the coating solution, and the appearance of the upper layer film becomes poor after coating and drying, and the corrosion resistance and chemical resistance tend to decrease. It was seen.

  In Examples 28, 29, and 30, a melamine resin was used as a curing agent for the binder resin, so that alkali resistance and workability tended to be lower than in the case of isocyanate curing.

  In Example 35, since the film thickness of the upper layer film was thick, there was a tendency for workability to decrease.

  According to the present invention, the distribution of the vanadium compound and the magnesium compound in the primer layer is controlled in the lower part of the layer, and the lower part of the primer layer does not form a portion having a low concentration of the vanadium compound and the magnesium compound, A precoated metal sheet having sufficient workability, excellent corrosion resistance and high chemical resistance can be obtained. Therefore, industrial applicability is high.

(1) The precoat metal plate which concerns on 1 aspect of this invention has a plating metal plate, the primer layer formed in the surface of the said plating metal plate, and the upper film formed in the surface of the said primer layer. The primer layer includes a binder resin and pigment particles containing a vanadium compound and a magnesium compound, and the vanadium compound is one or more selected from the group consisting of calcium vanadate, magnesium vanadate and ammonium metavanadate. And the magnesium compound is at least one selected from the group consisting of magnesium vanadate, magnesium oxide, magnesium hydroxide, and magnesium phosphate, and the plated metal plate in a cross section in the film thickness direction of the primer layer; Area within 1.0 μm from the interface with the primer layer in the film thickness direction When observed by EPMA mapping, a region where the detected concentration of vanadium element is less than 0.6% does not exist continuously in a direction perpendicular to the film thickness direction by 2.0 μm or more, and the detected concentration of magnesium element Is less than 3.0% continuously in the direction perpendicular to the film thickness direction.
(2) In the precoated metal plate according to (1), the primer layer has a thickness of 3 to 15 μm, and the maximum major axis in the thickness direction of the pigment particles is 80% of the thickness of the primer layer. It may be the following.
(3) As for the precoat metal plate as described in said (1) or (2), the said binder resin may also contain isocyanate resin.
(4) In the precoated metal plate according to any one of (1) to (3), the content of the pigment particles is 15 to 70% by mass with respect to the total solid mass of the primer layer. There may be .
( 5 ) The pre-coated metal plate according to any one of (1) to ( 4 ) may further have a chemical conversion treatment film between the plated metal plate and the primer layer.
( 6 ) In the precoated metal plate according to any one of (1) to ( 5 ), the plated metal plate may be a Zn-Al-Mg plated steel plate.

Claims (7)

A plated metal plate;
A primer layer formed on the surface of the plated metal plate;
An upper film formed on the surface of the primer layer;
Have
The primer layer includes a binder resin and pigment particles containing a vanadium compound and a magnesium compound,
When a region within 1.0 μm in the film thickness direction from the interface between the plated metal plate and the primer layer in the cross section in the film thickness direction of the primer layer is observed by EPMA mapping, the detected concentration of vanadium element is 0. A region that is less than .6% does not continuously exist in a direction perpendicular to the film thickness direction by 2.0 μm or more, and a region in which the magnesium element detection concentration is less than 3.0% is the film thickness direction. Does not exist continuously in the vertical direction for more than 2.0 μm,
A precoated metal sheet characterized by the above. The primer layer has a thickness of 3 to 15 μm,
The maximum major axis in the film thickness direction of the pigment particles is 80% or less of the film thickness of the primer layer.
The precoated metal sheet according to claim 1.   The pre-coated metal plate according to claim 1 or 2, wherein the binder resin contains an isocyanate resin. The pigment particle content is 15 to 70% by mass with respect to the total solid mass of the primer layer.
The precoated metal sheet according to any one of claims 1 to 3, wherein The vanadium compound is one or more selected from the group consisting of calcium vanadate, magnesium vanadate and ammonium metavanadate,
The magnesium compound is at least one selected from the group consisting of magnesium vanadate, magnesium oxide, magnesium hydroxide, and magnesium phosphate.
The precoat metal plate according to any one of claims 1 to 4, wherein   The precoated metal plate according to any one of claims 1 to 5, further comprising a chemical conversion treatment film between the plated metal plate and the primer layer.   The precoated metal plate according to any one of claims 1 to 6, wherein the plated metal plate is a Zn-Al-Mg plated steel plate.