JP7015403B2 - Black plated resin parts - Google Patents

Description

The present invention relates to black-plated resin parts used for decorative parts for vehicles, housing parts for electric appliances, and the like.

In the fields of decorative parts for vehicles and housing parts for electric appliances, there is an increasing need for a deep jet-black black appearance from the viewpoint of design. The jet-black color can be obtained by a black plating layer by cobalt chrome plating, chrome plating or the like.

There are some jet-black tones such as yellowish, bluish, and none of them, but market needs demand that they are not yellowish. The Applicant first focused on the problem that the jet-black color of the black plating layer made of trivalent chromium becomes yellowish when viewed through the chromate film formed as a corrosion-resistant film on it, and the corrosion-resistant film is phosphoric acid. It was shown that yellowing can be suppressed by forming a film made of chromium or molybdenum phosphate (Patent Document 1).

In Example 1 of Patent Document 1, the color tone of the black chrome plating layer seen through the corrosion-resistant film is 52.46 for L *, 0.67 for a *, and 4 for b * in the L * a * b * color system. It is .38, and there is only a slight yellowish tint. However, as a market need, there is a demand for a black color without yellowing.

Japanese Unexamined Patent Publication No. 2017-71100

Therefore, an object of the present invention is to provide a black plating resin component provided with a black chrome plating layer made of trivalent chromium without yellowing.

The present inventors have found that the state of chromium in the surface region of a black chromium plating layer made of trivalent chromium affects yellowing, and as a result of diligent studies, the present invention has been reached.

The present invention adopts the following means [1].
[1] Black chromium including a resin base material, a base plating layer formed on the resin base material, and a black chrome plating layer having a film thickness of 0.15 μm or more and made of trivalent chromium formed on the base plating layer. In plated resin parts
Chromium in the black chromium plating layer exists in the state of metallic chromium, chromium oxide and chromium hydroxide.
The surface region from the surface of the black chrome plating layer to a depth of at least 23 nm is a region of the surface alteration layer that has been altered with respect to the inside of the black chrome plating layer.
In the surface region, when the composition ratio of metallic chromium, chromium oxide and chromium hydroxide is a for metallic chromium, b for chromium oxide and c for chromium hydroxide (however, a> 0, b> 0, c>. 0), c> 41%, and c> 0.8b.
The black chrome plating layer measured from the surface region side is characterized in that b * in the L * a * b * color system is 3.0 or less.

[Action]
In the black chrome-plated layer made of trivalent chromium, the surface region is a region of the surface alteration layer having a depth of at least 23 nm from the surface, and has a relationship of c> 41% and c> 0.8b, and is a surface region. When b * in the L * a * b * color system of the black chrome plating layer measured from the side is 3.0 or less, the yellowish tint of the black chrome plating layer disappears. The mechanism has not been clarified yet, but it is presumed that a large amount of c is the main factor for reducing yellowness.

According to the present invention, it is possible to provide a black plating resin component provided with a black chrome plating layer made of trivalent chromium without yellowing.

It is a schematic cross-sectional view of the black-plated resin part of Samples 1-13. It is a graph which shows the relationship between the film thickness of the surface alteration layer in the black chrome plating layer of Samples 1 to 13 and a * or b *.

1. 1. Resin base material The resin of the resin base material may be thermoplastic or thermosetting, and is not particularly limited, but is limited to acrylonitrile, butadiene, and styrene copolymer (ABS) resin, polycarbonate (PC) resin, PC / ABS resin, and acrylic resin. , Stylus resin, polyamide resin, polypropylene resin, vinyl chloride resin, polyurethane resin and the like can be exemplified. ABS resin and PC / ABS resin are preferable from the viewpoint of strength, durability and the like.
On the resin base material, a conductive layer necessary for electrolytic plating the next base plating layer is formed. The conductive layer is not particularly limited, and an electroless nickel plating layer can be exemplified.

2. 2. Base plating layer The base plating layer preferably includes a copper plating layer and a nickel plating layer in this order. It is preferable that the uppermost layer of the base plating layer is a nickel plating layer, and a black chrome plating layer is formed on the nickel plating layer. Since the copper plating layer is highly ductile, it follows the resin base material well, and the nickel plating layer retains the aesthetic appearance of the black chrome plating layer and electrochemically protects it. The specific configuration of the nickel plating layer is not particularly limited, and may be one layer or a plurality of layers.

3. 3. Black chrome plating layer The reason why the film thickness of the black chrome plating layer is 0.15 μm or more as described above is to sufficiently hide the base plating layer and obtain a jet-black black color. The upper limit of the film thickness of the black chrome plating layer is not particularly limited, but is preferably 1 μm. If it exceeds 1 μm, the internal stress of the film becomes large and it becomes easy to crack.
The surface region (from the surface to a depth of at least 23 nm) is a region of the surface alteration layer that has been altered with respect to the inside (base material) of the black chrome plating layer as described above . As the surface alteration layer, a layer altered by oxygen, hydrogen or water vapor can be exemplified.

[About the color tone of the black chrome plating layer measured from the surface area side]
The reason why b * in the L * a * b * color system is 3 or less as described above is to eliminate the yellowish tint of black. It is more preferable that b * is 1 or less. This is because it has a slightly bluish black color and is more suitable for the needs of the market. The lower limit of b * is not particularly limited, but -10 is preferable. This is because if b * is less than -10, the bluish tint is strong and the use is limited.
a * is not particularly limited, but is preferably -3 to 3. This is because if a * is less than -3, the greenness is strong and the use is limited, and if it exceeds 3, the redness is strong and the use is limited.
L * is not particularly limited, but is preferably 30 to 54. This is because when L * is less than 30, the blackness is strong and the metallic feeling is reduced, and when it exceeds 54, the blackness is weak and the jet-black feeling is reduced.

When Fe is contained in the black chrome-plated layer, corrosion resistance is improved, which is preferable. Further, when the black chrome plating layer contains Co, Mn or Mo, the adhesion of the plating is improved, which is preferable.
The trivalent chromium compound used in the trivalent chromium plating bath is not particularly limited, but is limited to chromium sulfate (Cr ₂ (SO ₄ ) ₃ ), chrome alum (CrK (SO ₄ ) ₂ ), and chromium nitrate (Cr (NO ₃ )). ) ₃ ), chromium chloride (CrCl ₃ ), chromium acetate (Cr (CH ₃ COO) ₃ ) and the like can be exemplified.

4. Corrosion-resistant film It is preferable to provide a corrosion-resistant film on the black chrome plating layer. Examples of the corrosion-resistant film include a chromate film, a film made of chromium phosphate or molybdenum phosphate described in Patent Document 1, and the like. The film made of chromium phosphate or molybdenum phosphate preferably has a film thickness of 7 nm or more, and preferably 20 nm or less.

5. Applications of black-plated resin parts For vehicle decorative parts (radiator grills, fenders, garnishes, hubcaps, back panels, air spoilers, emblems, etc.), electrical products (mobile phones, smart phones, mobile information terminals, game consoles, etc.) Examples of housing parts can be used. In particular, decorative parts for vehicles exposed to wind and rain are required to have high corrosion resistance, and therefore are highly effective when the present invention is applied.

As the black-plated resin parts shown in FIG. 1, Samples 1 to 13 mainly showing the differences in Table 1 were prepared, and the black chrome-plated layer was analyzed and the color was measured.

[Common items of samples 1 to 13]
As shown in FIG. 1, the black-plated resin parts of Samples 1 to 13 are a resin base material made of ABS resin (with an electroless nickel plating layer as a conductive layer) and copper formed on the resin base material. A base plating layer containing a plating layer, a semi-bright nickel plating layer, a bright nickel plating layer, and a microporous nickel plating layer in this order, and a black chrome plating layer made of trivalent chrome formed on the nickel plating layer. It is equipped with. It is preferable to form a corrosion-resistant film on the black chrome plating layer, but samples 1 to 13 do not form a corrosion-resistant film.

In order to manufacture black-plated resin parts, first, the surface of the resin base material was pretreated in order to impart conductivity to the surface of the resin base material. In the pretreatment, the ABS resin base material is immersed in chromic acid and etched, and a metal complex of Pd-Sn is applied to the surface after the etching treatment to activate it, and then an electroless nickel plating layer as a conductive layer is formed. did.

Subsequently, a base plating treatment was performed on the resin base material to which the conductivity was imparted by the pretreatment. In the base plating process, the resin substrate is immersed in various metal plating baths and electrolytically plated so that the copper plating layer, the semi-bright nickel plating layer, the bright nickel plating layer, and the microporous nickel plating layer are laminated in this order. Was processed.

Next, a black chrome plating treatment was performed on the resin substrate that had been subjected to the base plating treatment. In the black chrome plating treatment, the base-plated resin substrate is immersed in a trivalent chrome plating bath, and the bath temperature is 40 ° C., the pH value is 3.2, the predetermined cathode current density, the predetermined anode current density, and the film formation rate are 0. This was performed by electrolytic plating under the conditions of 07 μm / min and a plating time of 5 minutes, whereby a black chrome plating layer having a predetermined thickness was formed on the microporous-nickel plating layer. The trivalent chromium plating bath used is an aqueous solution containing the following components (the trivalent chromium compound is basic chromium sulfate contained in trichromium azitibu), and the pH is further increased with 35% hydrochloric acid. The value was adjusted to 3.2.
Boric acid 63g / L manufactured by Wako Pure Chemical Industries
Atotech Trichrome Agitib 400g / L
Atotech Trichrome Stabilizer 100ml / L
Atotech Trichrome Regulator 3ml / L
Atotech Trichrome Collector 2ml / L
Atotech Trichrome Graphite Makeup 100ml / L
Atotech Trichrome Graphite Maintenance Prescribed formulation

[Differences between samples 1 to 13]
(1) In the black chrome plating treatment, the composition of Atotech's trichrome graphite maintenance (hereinafter referred to as "M agent") was set to 20 ml / L for samples 1 to 4 and 30 ml / L for samples 5 to 13. ..

(2) The cathode current density and the anode current density are set to 5 A / dm ² (Table 1 “Medium”) for Samples 9 and 12 and 2.5 A / dm ² (Table 1 “Low”) for Samples 8 and 11. Samples 1 to 7, 10 and 13 were set to 10 A / dm ² (Table 1 “high”).
Due to this difference in current density, the film thickness of the black chrome plating layer was 0.53 μm for samples 9 and 12, 0.252 μm for samples 8 and 11, and 1.10 μm for samples 1 to 7, 10 and 13.

(3) The state of the sample after the black chrome plating treatment and before the analysis and color measurement of the black chrome plating layer is set to immediately after plating for samples 8 to 10, and stored in vacuum for samples 2 and 5 (room temperature). Samples 3 and 6 were left in the air (leaved at room temperature for 18 days), and samples 1, 4, 7, 11 to 13 were subjected to an accelerated test (temperature 80 ° C. and humidity in a constant temperature bath). It was allowed to stand for a predetermined time in the air changing between 20% and 80% in 3 hours / cycle). The predetermined time for the accelerated test was 90 days for sample 1 and 18 days for samples 4, 7, 11 to 13.

For the black-plated resin parts of Samples 1 to 13 prepared as described above, the black chrome-plated layer was analyzed and the color was measured as follows.

<Analysis of black chrome plating layer>
Hard X-ray photoelectron spectroscopy (HAXPES) analysis of the black chrome plated layer was performed with the following equipment.
-Beamline: Large-scale radiation facility SPring-8 BL16XU (Photon energy: 7947.58eV)
-Analyzer: R4000 (Take-off angle: 85 °) from VG Scienta

Peak separation is performed by M. C. Biesinger et al. , Apple. Surf. Sci. 257,2717 (2011) was referred to (the oxide is a broad one). From the peak separation results of Cr2p, the following was found in all the samples.
-Chromium in the black chromium plating layer must be present in the state of metallic chromium (Cr), chromium oxide (Cr ₂ O ₃ ) and chromium hydroxide (Cr (OH) ₃ ).
-The composition ratio of metallic chromium, chromium oxide, and chromium hydroxide differs between the inside and the surface region of the black chromium plating layer, and the surface region has a depth of about 10 to several tens of nm from the surface of the black chromium plating layer. It is considered to be a surface alteration layer (even samples 8 to 10 immediately after plating are considered to be a surface alteration layer).

The film thickness of the surface alteration layer was determined by B.I. R. Streetmeier, Surf. Interface Anal. Calculated using 15, 51 (1990) (as Cr ₂ O ₃ / Cr).
Table 1 shows the film thickness of the surface alteration layer defined by the above and the composition ratio of metallic chromium, chromium oxide and chromium hydroxide. Table 1 shows (b + c) / a and c / b when the metallic chromium is a, the chromium oxide is b, and the chromium hydroxide is c.

<Color measurement>
The color tone (L * a * b * color system) of the black chrome plating layer was measured from the surface region side with a spectrocolorimeter (CM-700d manufactured by Konica Minolta). The measurement conditions were measurement mode SCI, observation condition 10 ° field of view, observation light source D65, and measurement diameter / illumination diameter = φ3 / φ6. Table 1 shows each value in the measured L * a * b * color system.

From these measurement results shown in Table 1, the following can be seen.
(1) The larger the amount of the M agent added, the larger the film thickness of the surface alteration layer.
(2) The higher the current density, the larger the film thickness of the surface alteration layer.
(3) As the state after the black chrome plating treatment changes from vacuum storage → leaving in the air → accelerated test, the film thickness of the surface alteration layer increases, metallic chromium a decreases, and the sum of chromium oxide and chromium hydroxide ( b + c) increases.
(4) The film thickness of the surface alteration layer of Samples 1 to 13 and a * and b * are plotted in FIG. From FIG. 2, a strong correlation is seen between the film thickness of the surface alteration layer and b *, and b * suddenly decreases in the range of 20 to 25 nm.

The samples 1, 4, 7, and 13 within the range of the present invention have no yellowish tint in the black chrome plating layer, and the samples 2, 3, 5, 6, 8 to 12 outside the range of the present invention are black chrome plated. There was a yellowish tint in the layer.

The present invention is not limited to the above embodiment, and can be appropriately modified and embodied without departing from the spirit of the invention.

Claims (2)

A black chrome plating resin component including a resin base material, a base plating layer formed on the resin base material, and a black chrome plating layer having a film thickness of 0.15 μm or more and made of trivalent chromium formed on the base plating layer. In
Chromium in the black chromium plating layer exists in the state of metallic chromium, chromium oxide and chromium hydroxide.
The surface region from the surface of the black chrome plating layer to a depth of at least 23 nm is a region of the surface alteration layer that has been altered with respect to the inside of the black chrome plating layer.
In the surface region, when the composition ratio of metallic chromium, chromium oxide and chromium hydroxide is a for metallic chromium, b for chromium oxide and c for chromium hydroxide (however, a> 0, b> 0, c>. 0), c> 41%, and c> 0.8b.
A black-plated resin component characterized in that b * in the L * a * b * color system of the black chrome-plated layer measured from the surface region side is 3.0 or less. The black-plated resin component according to claim 1, wherein the surface alteration layer is a layer altered by oxygen, hydrogen, or water vapor .

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