JP2012183784A - Elastomer with discontinuous metal coating and method for manufacturing the same - Google Patents

Elastomer with discontinuous metal coating and method for manufacturing the same Download PDF

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JP2012183784A
JP2012183784A JP2011049855A JP2011049855A JP2012183784A JP 2012183784 A JP2012183784 A JP 2012183784A JP 2011049855 A JP2011049855 A JP 2011049855A JP 2011049855 A JP2011049855 A JP 2011049855A JP 2012183784 A JP2012183784 A JP 2012183784A
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discontinuous metal
coat layer
layer
metal film
metal coating
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JP5702631B2 (en
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Yugo Asano
友吾 浅野
Takeshi Tsuda
健 津田
Haruo Okado
晴男 岡戸
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Inoac Corp
Tsuda Industries Co Ltd
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Inoue MTP KK
Inoac Corp
Tsuda Industries Co Ltd
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Abstract

PROBLEM TO BE SOLVED: To provide an elastomer with a discontinuous metal coating in which the discontinuous metal coating provided on the surface of a substrate formed of silicone rubber is hard to be peeled off from the substrate and also hard to be cracked.SOLUTION: The elastomer with the discontinuous metal coating includes steps for: laminating a primer coating layer 13 comprising a chlorinated polyolefin resin, an undercoat layer 15 comprising an acrylic resin or a polyurethane resin, a discontinuous metal coating 21 formed by vapor deposition and a top coat layer 25 on a silicone substrate 11 formed by peroxide crosslinking and having a D4 to D10 low molecular weight siloxane content of 300 PPM or smaller in this order; and making the top coat layer 25 by the same material as the undercoat layer 15.

Description

本発明は、シリコーンゴムからなる基材に不連続な金属被膜を設けた弾性体及びその製造方法に関する。   The present invention relates to an elastic body in which a discontinuous metal coating is provided on a base material made of silicone rubber, and a method for producing the same.

シリコーンゴムは弾性を有し、耐熱性、耐寒性、化学的安定性に優れるため、それらの機能が求められる用途に広く使用されている。また、シリコーンゴムの用途によっては、表面に金属被膜が求められる場合がある。   Silicone rubber has elasticity and is excellent in heat resistance, cold resistance, and chemical stability, and is therefore widely used in applications that require these functions. Moreover, depending on the use of silicone rubber, a metal coating may be required on the surface.

しかしながら、蒸着等の通常の金属被膜形成方法でシリコーンゴムの表面に金属被膜を形成した場合には、シリコーンゴムの引張りや屈曲等によって金属被膜が剥がれたり、金属被膜に亀裂を生じたりするおそれがある。   However, when a metal film is formed on the surface of the silicone rubber by a normal metal film forming method such as vapor deposition, the metal film may be peeled off due to the tension or bending of the silicone rubber, or the metal film may be cracked. is there.

なお、金属被膜の剥がれや亀裂の防止を防ぐ方法として、軟調樹脂材料からなる基材に結晶粒界を有する厚さ150Å以上800Å以下の金属薄膜層を形成したり(特許文献1)、金属粒子の薄膜層を基材の表面に形成した後に基材全体を熱膨張させて金属粒子層に微細な溝状クラックを発生さたり(特許文献2)、金属を蒸着装置の空間内に均一かつ直線的に飛散させることによって、長手方向の最大長が5μm以内の蒸着金属粒からなる多数の島部が不連続に密集する平坦な表面構造を有し、層厚が20nm〜100nmからなる金属薄膜層をシリコーンゴムに形成する方法(特許文献3)がある。   In addition, as a method for preventing the peeling and cracking of the metal film, a metal thin film layer having a grain boundary of 150 to 800 mm is formed on a base material made of a soft resin material (Patent Document 1), or metal particles After the thin film layer is formed on the surface of the base material, the entire base material is thermally expanded to generate fine groove-like cracks in the metal particle layer (Patent Document 2). Metal thin film layer having a flat surface structure in which a large number of island parts made of vapor-deposited metal grains having a maximum length in the longitudinal direction of 5 μm or less are concentrated discontinuously and having a layer thickness of 20 nm to 100 nm There is a method (Patent Document 3) for forming a silicone rubber.

特開平11−34220号公報JP-A-11-34220 特開平11−131213号公報JP-A-11-131213 特開2007−136689号公報Japanese Patent Laid-Open No. 2007-136689

しかしながら従来における金属被膜の剥がれや亀裂を防ぐ方法では、金属被膜の剥がれや亀裂の防止が充分ではなかった。
本発明は前記の点に鑑みなされたものであって、金属被膜の剥がれや亀裂を生じ難い不連続な金属皮膜を有する弾性体とその製造方法の提供を目的とする。
However, the conventional method for preventing peeling or cracking of the metal coating has not been sufficient to prevent peeling or cracking of the metal coating.
This invention is made | formed in view of the said point, Comprising: It aims at provision of the elastic body which has a discontinuous metal film which is hard to produce peeling and a crack of a metal film, and its manufacturing method.

請求項1の発明は、パーオキサイド架橋により形成され、D4〜D10の低分子シロキサンの含有量が300PPM以下であるシリコーン基材上に、塩素化ポリオレフィン系樹脂からなるプライマーコート層と、アクリル系樹脂又はポリウレタン系樹脂からなるアンダーコート層と、蒸着により形成された不連続な金属被膜と、トップコート層がこの順に積層され、前記トップコート層が前記アンダーコート層と同材料からなることを特徴とする不連続な金属被膜を有する弾性体に係る。   The invention according to claim 1 is a primer coat layer made of a chlorinated polyolefin resin and an acrylic resin on a silicone substrate formed by peroxide crosslinking and having a content of low molecular siloxanes of D4 to D10 of 300 PPM or less. Alternatively, an undercoat layer made of a polyurethane resin, a discontinuous metal film formed by vapor deposition, and a topcoat layer are laminated in this order, and the topcoat layer is made of the same material as the undercoat layer. The present invention relates to an elastic body having a discontinuous metal coating.

請求項2の発明は、パーオキサイド架橋により形成されるシリコーンゴムからなる基材に蒸着された不連続な金属被膜を有する弾性体の製造方法であって、前記基材を180〜200℃で1〜12時間加熱処理した後、前記基材表面にフレーム処理、コロナ放電処理、プラズマ処理の群から一つ選択される表面処理を施し、前記基材の表面に塩素化ポリオレフィン系樹脂からなるプライマーコート層とアンダーコート層を順に形成した後、蒸着により不連続な金属被膜を形成し、前記不連続な金属被膜上に前記アンダーコート層と同材料からなるトップコート層を形成することを特徴とする不連続な金属被膜を有する弾性体の製造方法に係る。 Invention of Claim 2 is a manufacturing method of the elastic body which has a discontinuous metal film vapor-deposited on the base material which consists of silicone rubber formed by peroxide bridge | crosslinking, Comprising: The said base material is 180-200 degreeC, and is 1 After heat treatment for 12 hours, the surface of the base material is subjected to a surface treatment selected from the group of flame treatment, corona discharge treatment, and plasma treatment, and the surface of the base material is made of a chlorinated polyolefin resin. A layer and an undercoat layer are formed in order, a discontinuous metal film is formed by vapor deposition, and a topcoat layer made of the same material as the undercoat layer is formed on the discontinuous metal film. The present invention relates to a method for producing an elastic body having a discontinuous metal coating.

請求項3の発明は、請求項2において、前記プライマーコート層は塩素化ポリオレフィン系樹脂からなり、前記アンダーコート層とトップコート層はアクリル系樹脂又はポリウレタン系樹脂からなることを特徴とする。 The invention of claim 3 is characterized in that, in claim 2, the primer coat layer is made of a chlorinated polyolefin resin, and the undercoat layer and the top coat layer are made of an acrylic resin or a polyurethane resin.

本発明によれば、蒸着により形成された不連続な金属被膜を、同じ材料からなるトップコート層とアンダーコート層で挟んだことにより、不連続な金属被膜が弾性体の曲げ等によっても剥がれ難くなると共に亀裂を生じ難くなる。さらに本発明の製造方法によれば、パーオキサイド架橋により形成されるシリコーンゴムからなる基材を180〜200℃にて1〜12時間加熱した後に蒸着により金属被膜を形成しているため、シリコーンゴムに含まれるD4〜D10の低分子シロキサンの含有量が300PPM以下となって、製造された金属被膜は弾性体の曲げ等によっても剥がれ難くなると共に亀裂を生じ難くなる。なお、本発明における「不連続な金属被膜」は、金属被膜が一面に連続せず、平面方向の最大長さが10μm以内の多数の蒸着金属粒体が島状に互いに離間して又は一部接触した状態で平面形状を形成している金属被膜の意味である。   According to the present invention, a discontinuous metal film formed by vapor deposition is sandwiched between a top coat layer and an undercoat layer made of the same material, so that the discontinuous metal film is hardly peeled off even by bending of an elastic body. It becomes hard to produce a crack with becoming. Furthermore, according to the production method of the present invention, the metal film is formed by vapor deposition after heating the base material made of silicone rubber formed by peroxide crosslinking at 180 to 200 ° C. for 1 to 12 hours. The content of the low molecular siloxanes of D4 to D10 contained in is less than or equal to 300 PPM, and the manufactured metal film is difficult to be peeled and cracked even by bending of the elastic body. The “discontinuous metal coating” in the present invention is a metal coating that is not continuous on one side, and a large number of vapor-deposited metal particles having a maximum length in the plane direction of 10 μm or less are separated from each other in an island shape or partially. It is the meaning of the metal film which forms the planar shape in the state which contacted.

本発明の製造方法で製造された不連続な金属被膜を有する弾性体の拡大断面図である。It is an expanded sectional view of the elastic body which has the discontinuous metal film manufactured with the manufacturing method of this invention.

図1に示す不連続な金属被膜を有する弾性体10は、本発明の不連続な金属被膜を有する弾性体の製造方法によって製造されたものであり、基材11の表面にプライマーコート層13、アンダーコート層15、不連続な金属被膜21、トップコート層25が順に形成されたものからなる。   An elastic body 10 having a discontinuous metal film shown in FIG. 1 is manufactured by the method for manufacturing an elastic body having a discontinuous metal film according to the present invention. The undercoat layer 15, the discontinuous metal coating 21, and the topcoat layer 25 are sequentially formed.

前記基材11は、シリコーンゴムからなる。シリコーンゴムとしては、パーオキサイド架橋により形成され、加熱処理によって、D4〜D10の低分子シロキサンの含有量が300PPM以下となったものが、前記プライマーコート層13との密着性を良好にできるために好ましいものである。前記基材11の厚みは、前記金属被膜を有する弾性体10の用途等に応じて決定される。   The substrate 11 is made of silicone rubber. The silicone rubber is formed by peroxide crosslinking, and the content of the low molecular siloxane of D4 to D10 becomes 300 PPM or less by heat treatment, so that the adhesion with the primer coat layer 13 can be improved. It is preferable. The thickness of the base material 11 is determined according to the use of the elastic body 10 having the metal coating.

前記プライマーコート層13は、蒸着による金属被膜21の形成を良好に行うために設けられ、ポリオレフィン系樹脂、塩素化ポリオレフィン系樹脂、エポキシ系樹脂、アクリル系樹脂、ポリエステル系樹脂、ポリウレタン系樹脂等からなる。耐候性、耐酸・アルカリ性に優れた塩素化ポリオレフィン系樹脂が好ましく、アンダーコート層との相溶性を考慮して、エポキシや無水マレイン酸等の極性基をもった化合物で変成されているものがさらに好ましい。前記プライマーコート層13の厚みは2〜4μmが好ましい。   The primer coat layer 13 is provided to satisfactorily form the metal coating 21 by vapor deposition, and is made of a polyolefin resin, a chlorinated polyolefin resin, an epoxy resin, an acrylic resin, a polyester resin, a polyurethane resin, or the like. Become. A chlorinated polyolefin resin excellent in weather resistance, acid resistance and alkali resistance is preferable. In consideration of compatibility with the undercoat layer, a resin modified with a compound having a polar group such as epoxy or maleic anhydride is further added. preferable. The primer coat layer 13 preferably has a thickness of 2 to 4 μm.

前記アンダーコート層15は、蒸着による金属被膜21の形成を良好に行うために前記プライマーコート層13の表面に設けられ、エポキシ系樹脂、アクリル系樹脂、ポリエステル系樹脂、ポリウレタン系樹脂等からなる。プライマーコート層に塩素化ポリオレフィン系樹脂を用いた場合、ポリウレタン系樹脂またはアクリル形樹脂が好ましい。前記アンダーコート層15の厚みは10〜12μmが好ましい。   The undercoat layer 15 is provided on the surface of the primer coat layer 13 in order to satisfactorily form the metal coating 21 by vapor deposition, and is made of an epoxy resin, an acrylic resin, a polyester resin, a polyurethane resin, or the like. When a chlorinated polyolefin resin is used for the primer coat layer, a polyurethane resin or an acrylic resin is preferable. The thickness of the undercoat layer 15 is preferably 10 to 12 μm.

前記不連続な金属被膜21は、前記基材11に金属調を付与するために設けられている。前記金属被膜21の厚みは、400Å〜1000Åが好ましい。前記金属被膜21を構成する金属の種類は、アルミニウム、クロム、銅、銀、金、ゲルマニウム、インジウム、鉄、マグネシウム、ニッケル、錫、亜鉛などが挙げられる。それらの中でも、アルミニウム、インジウム、マグネシウム等は好ましいものである。   The discontinuous metal coating 21 is provided for imparting a metallic tone to the substrate 11. The thickness of the metal coating 21 is preferably 400 to 1000 mm. Examples of the metal constituting the metal coating 21 include aluminum, chromium, copper, silver, gold, germanium, indium, iron, magnesium, nickel, tin, and zinc. Among these, aluminum, indium, magnesium and the like are preferable.

前記トップコート層25は、前記不連続な金属被膜21の表面保護のために設けられ、エポキシ系樹脂、アクリル系樹脂、ポリエステル系樹脂、ポリウレタン系樹脂等からなる。前記トップコート層25の厚みは10〜12μmが好ましい。前記トップコート層25は、不連続な金属被膜21を通過してアンダーコート層15と接着して不連続な金属被膜を21挟み込むことからトップコート層25は、アンダーコート層15と同じ樹脂が好ましい。   The top coat layer 25 is provided for protecting the surface of the discontinuous metal coating 21, and is made of an epoxy resin, an acrylic resin, a polyester resin, a polyurethane resin, or the like. The thickness of the top coat layer 25 is preferably 10 to 12 μm. Since the top coat layer 25 passes through the discontinuous metal film 21 and adheres to the undercoat layer 15 to sandwich the discontinuous metal film 21, the top coat layer 25 is preferably made of the same resin as the undercoat layer 15. .

次に、前記不連続な金属被膜を有する弾性体10の製造方法について説明する。
まず、シリコーンゴムからなる前記基材11を加熱する。シリコーンゴムの製造は、シリコーンポリマー、パーオキサイド加硫剤および必要に応じて顔料などの添加物を加えた材料をオープンロールにて混練させる。混練後、適当な厚みにシーティングし、熱プレスにて適宜の成型温度、圧力にて加硫し、成型を行う。
Next, the manufacturing method of the elastic body 10 which has the said discontinuous metal film is demonstrated.
First, the base material 11 made of silicone rubber is heated. In the production of silicone rubber, a material to which a silicone polymer, a peroxide vulcanizing agent and, if necessary, an additive such as a pigment are added is kneaded with an open roll. After kneading, sheeting is performed to an appropriate thickness, and vulcanization is performed by a hot press at an appropriate molding temperature and pressure to perform molding.

前記基材11の加熱は、前記基材11を構成するシリコーンゴムに含まれる低分子シロキサンやシリコーンオイルなどの未反応物を、強制的に前記基材11から除去するために行われる。低分子シロキサンやシリコーンオイルなどの未反応物が前記基材11の表面や内部に多く存在していると、その後に形成する前記プライマーコート層13と前記基材11との密着性が悪くなって、前記金属被膜21が前記基材11から剥離しやすくなると共に、前記金属被膜21の亀裂を生じやすくなる。なお、前記加熱を行わなかった場合と、前記加熱を行った場合とにおける前記金属被膜21の剥離や亀裂のし難さの差は、前記金属被膜を有する弾性体10の製造直後では小さいが、製造後からの期間が長くなるほど大きくなる。   The substrate 11 is heated to forcibly remove unreacted substances such as low-molecular siloxane and silicone oil contained in the silicone rubber constituting the substrate 11 from the substrate 11. If a large amount of unreacted substances such as low molecular weight siloxane and silicone oil are present on the surface or inside of the base material 11, the adhesion between the primer coat layer 13 and the base material 11 formed thereafter deteriorates. The metal film 21 is easily peeled off from the base material 11 and the metal film 21 is easily cracked. The difference in the difficulty of peeling and cracking of the metal coating 21 between the case where the heating is not performed and the case where the heating is performed is small immediately after the production of the elastic body 10 having the metal coating, The longer the period after manufacture, the larger the period.

前記加熱温度は180〜200℃が好ましい。前記加熱温度が180℃未満の場合には、低分子シロキサンやシリコーンオイルなどの未反応物をシリコーンゴムから充分に除去できなくなり、前記金属被膜21の剥離や亀裂防止効果が低くなる。一方、前記加熱温度が200℃よりも高い場合には、加熱によってシリコーンゴムが変形しやすい。また、前記加熱の時間は1〜12時間が好ましい。特に好ましくは2〜6時間である。1時間よりも短い加熱は低分子シロキサンやシリコーンオイルなどの未反応物をシリコーンゴムから充分に除去できず、D4〜D10の低分子シロキサンの含有量が300PPMより大きくなって、密着性が低下する。一方、12時間より長い加熱は、製造効率が悪くなる。   The heating temperature is preferably 180 to 200 ° C. When the heating temperature is lower than 180 ° C., unreacted substances such as low molecular siloxane and silicone oil cannot be sufficiently removed from the silicone rubber, and the effect of preventing the metal film 21 from peeling and cracking is reduced. On the other hand, when the heating temperature is higher than 200 ° C., the silicone rubber is easily deformed by heating. The heating time is preferably 1 to 12 hours. Especially preferably, it is 2 to 6 hours. Heating shorter than 1 hour cannot sufficiently remove unreacted substances such as low-molecular siloxane and silicone oil from the silicone rubber, and the content of low-molecular siloxanes D4 to D10 is greater than 300 PPM, resulting in decreased adhesion. . On the other hand, when the heating is longer than 12 hours, the production efficiency is deteriorated.

前記基材11の加熱後、フレーム処理、コロナ放電処理、プラズマ処理の群から一つ選択される表面処理を施す。例えばフレーム処理は、ガスバーナーで前記基材11の表面を焼いて接着性を向上する方法であり、一般的には、極性の低い基材11の表面をガスの炎であぶることで、基材11の表面の分子に極性を持たせることができ、濡れ性を向上させることができる。また、前記基材11の表面に極性を持たせる塩基などを生じさせるコロナ放電処理、プラズマ処理でもフレーム処理と同様に接着性を向上させることができる。   After the substrate 11 is heated, a surface treatment selected from the group of flame treatment, corona discharge treatment, and plasma treatment is performed. For example, the flame treatment is a method of improving the adhesion by baking the surface of the base material 11 with a gas burner. Generally, the surface of the base material 11 having a low polarity is blown with a gas flame to The molecules on the surface of 11 can be polar and the wettability can be improved. Also, the corona discharge treatment or plasma treatment that generates a base having a polarity on the surface of the substrate 11 can improve the adhesion as in the frame treatment.

前記表面処理後、前記基材11の表面にプライマーコート層13とアンダーコート層15を所定の厚みで順に形成する。前記プライマーコート層13とアンダーコート層15の形成は、スプレー塗布等の公知の塗布方法によって行われる。前記プライマーコート層13及びアンダーコート層15は、それぞれ塗布後に乾燥硬化が行われる。   After the surface treatment, a primer coat layer 13 and an undercoat layer 15 are sequentially formed on the surface of the substrate 11 with a predetermined thickness. The primer coat layer 13 and the undercoat layer 15 are formed by a known coating method such as spray coating. The primer coat layer 13 and the undercoat layer 15 are each dried and cured after application.

次に、前記アンダーコート層15の表面に、蒸着によって前記不連続な金属被膜21を形成する。前記蒸着は、公知の方法で行われる。特にスパッタリングなどの物理的蒸着が好ましい。前記蒸着は、前記金属被膜21が所定厚み、好ましくは400Å〜1000Åとなるようにして行う。   Next, the discontinuous metal film 21 is formed on the surface of the undercoat layer 15 by vapor deposition. The said vapor deposition is performed by a well-known method. In particular, physical vapor deposition such as sputtering is preferable. The vapor deposition is performed so that the metal coating 21 has a predetermined thickness, preferably 400 to 1000 mm.

前記金属被膜21を形成した後、前記金属被膜21の表面に前記トップコート層25を所定厚みで形成する。前記トップコート層25の形成は、スプレー塗布等によって行われる。これによって、前記金属被膜を有する弾性体10が得られる。   After the metal coating 21 is formed, the top coat layer 25 is formed on the surface of the metal coating 21 with a predetermined thickness. The top coat layer 25 is formed by spray coating or the like. Thereby, the elastic body 10 having the metal film is obtained.

グレード:TSE−221−5UC、モメンティブ・パフォーマンス・マテリアルズ社、100重量部と、グレード:TC−8、モメンティブ・パフォーマンス・マテリアルズ社、5重量部とからなるシリコーンゴム(パーオキサイド架橋により形成されたもの)を裁断して、厚み2mm、一辺100mmの正方形板状体からなる基材を作成した。   Grade: TSE-221-5UC, Momentive Performance Materials, 100 parts by weight, Grade: TC-8, Momentive Performance Materials, 5 parts by weight silicone rubber (formed by peroxide crosslinking) And a base material made of a square plate having a thickness of 2 mm and a side of 100 mm was prepared.

前記基材を恒温層に収容して、表1の加熱温度及び加熱時間で基材の加熱を行った。その後、前記基材を恒温槽から取り出して自然冷却し、低分子シロキサン量を測定した。なお、シリコーンゴムのサンプル片0.5gを、アセトンを5ml中に12時間浸漬したものを試験液とし、1μlをガスクロマトグラフ(島津製作所GC−17A)にて測定し、ケイ素数4〜10の環状体及び非環状体の総量(D4〜D10)を低分子シロキサン量として定量した。冷却後の基材の片面に、ガスバーナーの炎を当てることによりフレーム処理を行った。次に、フレーム処理後の基材の片面にプライマー塗料をスプレー塗装し、その後70℃で3分間乾燥させて厚み3μmのプライマーコート層を基材の表面に形成した。使用したプライマー塗料は、ポリプロピレン用プライマー、品番:S−No.54 PPプライマーNo.2(塩素化ポリオレフィン系樹脂)、長島特殊塗料(株)である。   The base material was accommodated in a thermostatic layer, and the base material was heated at the heating temperature and heating time shown in Table 1. Then, the said base material was taken out from the thermostat, naturally cooled, and the amount of low molecular siloxane was measured. In addition, 0.5 g of silicone rubber sample pieces were immersed in 5 ml of acetone for 12 hours, and 1 μl was measured with a gas chromatograph (Shimadzu GC-17A). The total amount of the body and the non-cyclic body (D4 to D10) was quantified as the amount of low molecular siloxane. Flame treatment was performed by applying a flame of a gas burner to one side of the cooled substrate. Next, the primer coating was spray-coated on one side of the base material after the frame treatment, and then dried at 70 ° C. for 3 minutes to form a primer coating layer having a thickness of 3 μm on the surface of the base material. The primer paint used was a primer for polypropylene, product number: S-No. 54 PP primer no. 2 (chlorinated polyolefin resin), Nagashima Special Paint Co., Ltd.

プライマーコート層の表面に、アンダー塗料をスプレー塗装し、その後70℃で3分の予備加熱、続いて80℃で120分の乾燥を行い、厚み11μmのアンダーコート層を形成した。使用したアンダー塗料の配合は、アクリル樹脂系塗料の塗料液、品番:オリジンプレートZ クリヤ、オリジン電気(株)、400重量部、アクリル樹脂系塗料の硬化剤、品番:ポリハードR、オリジン電気(株)、100重量部、アクリル系樹脂塗料のシンナー、品番:プラネット シンナー#D210、オリジン電気(株)、300重量部である。   Undercoat was spray-coated on the surface of the primer coat layer, followed by preheating at 70 ° C. for 3 minutes, followed by drying at 80 ° C. for 120 minutes to form an undercoat layer having a thickness of 11 μm. The composition of the under paint used is: paint solution of acrylic resin paint, part number: Origin Plate Z Clear, Origin Electric Co., Ltd., 400 parts by weight, curing agent for acrylic resin paint, part number: Polyhard R, Origin Electric Co., Ltd. ), 100 parts by weight, thinner of acrylic resin paint, product number: Planet Thinner # D210, Origin Electric Co., Ltd., 300 parts by weight.

プライマーコート層及びアンダーコート層形成後の基材を、真空蒸着装置に収容し、インジウム、純度99.99%、長さ45mm、真空度3.0×10−2Pa、余熱1 1100A/15A、余熱2 1200A/15A、蒸着1350A/15Aで蒸着を行い、厚み600Åの不連続な金属被膜をアンダーコート層の表面に形成した。 The base material after forming the primer coat layer and the undercoat layer is accommodated in a vacuum deposition apparatus, indium, purity 99.99%, length 45 mm, degree of vacuum 3.0 × 10 −2 Pa, residual heat 1 1100 A / 15 A, Deposition was performed with residual heat 2 1200A / 15A and vapor deposition 1350A / 15A, and a discontinuous metal film having a thickness of 600 mm was formed on the surface of the undercoat layer.

次に、不連続な金属被膜の表面に、トップ塗料をスプレー塗装し、その後70℃で3分の予備加熱、続いて70℃で120分の乾燥を行い、厚み11μmのトップコート層を形成し、実施例1〜5の金属被膜を有する弾性体を製造した。使用したトップ塗料は、アンダー塗料と同じものであり、アクリル樹脂系塗料の塗料液、品番:オリジンプレートZ クリヤ、オリジン電気(株)、400重量部、アクリル樹脂系塗料の硬化剤、品番:ポリハードR、オリジン電気(株)、100重量部、アクリル系樹脂塗料のシンナー、品番:プラネット シンナー#D210、オリジン電気(株)、300重量部、スリップ剤、品番:4001、東邦化研工業(株)、24重量部である。   Next, a top coating is spray-coated on the surface of the discontinuous metal coating, followed by preheating at 70 ° C. for 3 minutes, followed by drying at 70 ° C. for 120 minutes to form a topcoat layer having a thickness of 11 μm. The elastic body which has a metal film of Examples 1-5 was manufactured. The top paint used is the same as the under paint. Acrylic resin paint liquid, part number: Origin Plate Z Clear, Origin Electric Co., Ltd., 400 parts by weight, acrylic resin paint curing agent, part number: Polyhard R, Origin Electric Co., Ltd., 100 parts by weight, acrylic resin paint thinner, product number: Planet Thinner # D210, Origin Electric Co., Ltd., 300 parts by weight, slip agent, product number: 4001, Toho Kaken Kogyo Co., Ltd. 24 parts by weight.

一方、前記実施例と同じシリコーンゴムを用いて、前記金属被膜の形成前に加熱を行わないためD4〜D10の低分子シロキサンの含有量が5300であった比較例1、前記実施例と同じシリコーンゴムを用いて前記加熱温度を150℃、加熱時間を3時間としたためD4〜D10の低分子シロキサンの含有量が1700であった比較例2、前記実施例と同じシリコーンゴムを用いて前記加熱温度を180℃、加熱時間を0.5時間としたためD4〜D10の低分子シロキサンの含有量が330であった比較例3、白金触媒による付加反応型シリコーン(RTV)ゴムを用いた以外は、すべて前記実施例5と同様に行った比較例4の不連続な金属被膜を有する弾性体をそれぞれ製造した。   On the other hand, the same silicone rubber as in the above example was used, and heating was not performed before the metal coating was formed, so the content of low molecular siloxanes D4 to D10 was 5300, and the same silicone as in the above example. Comparative Example 2 in which the content of the low molecular siloxane of D4 to D10 was 1700 because the heating temperature was set to 150 ° C. and the heating time was set to 3 hours using rubber. Comparative Example 3 in which the content of low molecular siloxanes of D4 to D10 was 330 because the heating time was set to 180 ° C. and the heating time was 0.5 hours, except that an addition reaction type silicone (RTV) rubber using a platinum catalyst was used. The elastic bodies having the discontinuous metal coating of Comparative Example 4 performed in the same manner as in Example 5 were produced.

Figure 2012183784
Figure 2012183784

各実施例及び各比較例について、変形・変色の有無確認、製造直後の碁盤目試験、2ヶ月保存後の碁盤目試験、製造直後の引張り試験、2ヶ月保存後の引張り試験を行った。
変形・変色の有無は、製造後の各実施例及び各比較例について、基材が変色(色抜け)しているか、歪みが発生しているかを目視で判断し、変色と変形の何れも無い場合には「無」、何れか一方でも有る場合には「有」とした。
About each Example and each comparative example, the presence or absence of a deformation | transformation and discoloration, the cross-cut test immediately after manufacture, the cross-cut test after 2 months storage, the tensile test immediately after manufacture, and the tensile test after 2 months storage were done.
The presence / absence of deformation / discoloration is determined by visual observation of whether the base material is discolored (color loss) or distortion occurs in each of the Examples and Comparative Examples after production, and there is no discoloration or deformation. “None” in the case, and “Yes” in either case.

製造直後の碁盤目試験は、製造直後の各実施例及び各比較例におけるトップコート層の表面に、1.5mm間隔で100升の碁盤目状の切り傷を付け、100升上にセロハンテープを密着させて剥離し、トップコート層が剥離していない升の数を数えた。
2ヶ月保存後の碁盤目試験は、各実施例及び各比較例を製造後、室内(常温保存)に2ヶ月保存した後、各実施例及び各比較例におけるトップコート層の表面に、1.5mm間隔で100升の碁盤目状の切り傷を付け、100升上にセロハンテープを密着させて剥離し、トップコート層が剥離しなかった升の数を数えた。
In the cross cut test immediately after the manufacture, the surface of the top coat layer in each of the examples and the comparative examples immediately after the manufacture is cut with a 100 cut grid pattern at intervals of 1.5 mm, and the cellophane tape is adhered to the top of the 100 coat. The number of wrinkles that were peeled off and the topcoat layer was not peeled was counted.
The cross cut test after storage for 2 months was carried out after the production of each Example and each Comparative Example and after storage in the room (room temperature storage) for 2 months, on the surface of the topcoat layer in each Example and each Comparative Example. 100 mm grid-like cuts were made at intervals of 5 mm, and the cellophane tape was adhered and peeled onto 100 mm, and the number of wrinkles on which the topcoat layer did not peel was counted.

製造直後の引張り試験は、製造直後の各実施例及び各比較例に対して、オートグラフによる引張り試験を行って、基材からプライマーコート層、アンダーコート層、金属被膜及びトップコート層が剥がれたか否かを目視で判断した。
2ヶ月保存後の引張り試験は、各実施例及び各比較例を製造後、室内(常温保存)に2ヶ月保存した後、各実施例及び各比較例に対して、オートグラフによる引張り試験(JIS K6251 ダンベル3号)を伸び率100%となるように行って、基材からプライマーコート層、アンダーコート層、金属被膜及びトップコート層が剥がれたか否かを目視で判断した。
In the tensile test immediately after production, whether the primer coat layer, the undercoat layer, the metal coating, and the top coat layer were peeled off from the substrate by performing a tensile test by autograph for each example and each comparative example immediately after production. It was judged visually.
The tensile test after storage for 2 months was conducted after each example and each comparative example was manufactured and stored indoors (stored at room temperature) for 2 months, and then for each example and each comparative example, an autograph tensile test (JIS K6251 Dumbbell No. 3) was performed so that the elongation was 100%, and it was visually determined whether or not the primer coat layer, the undercoat layer, the metal coating, and the top coat layer were peeled off from the substrate.

結果を前記表1に示す。表1に示す通り、実施例1〜実施例8は、製造直後及び2ヶ月保存後の何れにおいても碁盤目試験結果が100/100であり、また、引張り試験結果は剥がれの無いものであった。さらに、実施例1〜実施例8の何れも変形、変色が無かった。   The results are shown in Table 1. As shown in Table 1, in Examples 1 to 8, the cross-cut test result was 100/100 immediately after production and after storage for 2 months, and the tensile test result was not peeled off. . Further, none of Examples 1 to 8 was deformed or discolored.

一方、加熱を行わないためD4〜D10の低分子シロキサンの含有量が高い比較例1は、製造直後の碁盤目試験結果が100/100、製造直後の引張り試験結果が剥がれ無しであったが、2ヶ月保存後の碁盤目試験結果が50/100であり、しかも2ヶ月保存後の引張り試験結果が剥がれ有りであり、長期間経過後に金属被膜が剥がれやすくなることがわかる。また、加熱温度が150℃と低いため、D4〜D10の低分子シロキサンの含有量が高い比較例2は、製造直後の碁盤目試験結果が100/100、製造直後の引張り試験結果が剥がれ無しであったが、2ヶ月保存後の碁盤目試験結果が90/100であってしかも2ヶ月保存後の引張り試験結果が剥がれ有りであり、長期間経過後に金属被膜が剥がれやすくなることがわかる。また、加熱温度が0.5時間と短くD4〜D10の低分子シロキサンの含有量が高い比較例3は、製造直後の碁盤目試験結果が100/100、製造直後の引張り試験結果が剥がれ無しであったが、2ヶ月保存後の碁盤目試験結果が90/100であってしかも2ヶ月保存後の引張り試験結果が剥がれ有りであり、長期間経過後に金属被膜が剥がれやすくなることがわかる。また、比較例4は、白金触媒による付加反応型シリコーン(RTV)で、実施例5と同条件で蒸着をしたが、製造直後の碁盤目試験結果が50/100であった。   On the other hand, in Comparative Example 1 in which the content of the low molecular siloxanes D4 to D10 is high because no heating is performed, the cross-cut test result immediately after manufacture is 100/100, and the tensile test result immediately after manufacture is not peeled off. It can be seen that the cross-cut test result after storage for 2 months is 50/100, the tensile test result after storage for 2 months is peeled off, and the metal film is easily peeled off after a long period of time. Moreover, since the heating temperature is as low as 150 ° C., Comparative Example 2 in which the content of the low molecular siloxane of D4 to D10 is high is 100/100 for the cross-cut test result immediately after manufacture, and the tensile test result immediately after manufacture is not peeled off. However, it was found that the cross-cut test result after storage for 2 months was 90/100 and the tensile test result after storage for 2 months was peeled off, and the metal film was easily peeled off after a long period of time. Further, Comparative Example 3 having a heating temperature as short as 0.5 hours and a high content of low molecular weight siloxane of D4 to D10 has a cross-cut test result immediately after manufacture of 100/100, and a tensile test result immediately after manufacture does not peel off. However, it was found that the cross-cut test result after storage for 2 months was 90/100 and the tensile test result after storage for 2 months was peeled off, and the metal film was easily peeled off after a long period of time. In addition, Comparative Example 4 was an addition reaction type silicone (RTV) using a platinum catalyst, and vapor deposition was performed under the same conditions as in Example 5. However, the cross-cut test result immediately after production was 50/100.

また、プライマーコート層の種類による不連続な金属被膜の剥がれ難さの違いを確認するため、実施例2における塩素化ポリオレフィン系樹脂のプライマー塗料に代えて、プライマー塗料をアクリル系樹脂塗料とした比較例5の不連続な金属被膜を有する弾性体と、プライマー塗料をポリウレタン系樹脂とした比較例6の不連続な金属被膜を有する弾性体を、実施例2と同じ条件で製造し、前記製造直後の碁盤目試験を行った。   Moreover, in order to confirm the difference in the difficulty of peeling of the discontinuous metal film depending on the type of the primer coat layer, a comparison was made in which the primer paint was replaced with an acrylic resin paint instead of the primer paint of the chlorinated polyolefin resin in Example 2. The elastic body having the discontinuous metal coating of Example 5 and the elastic body having the discontinuous metal coating of Comparative Example 6 in which the primer coating was made of polyurethane resin were produced under the same conditions as in Example 2, and immediately after the production. A cross-cut test was conducted.

その結果は、表2に示す通りであり、プライマー塗料を塩素化ポリオレフィン系樹脂とした実施例2は100升の全てが剥離しなかった(100/100)のに対し、プライマー塗料をアクリル系樹脂塗料とした比較例5及びプライマー塗料をポリウレタン系樹脂とした比較例6は、何れも100升の全てが剥離した(100/100)という結果であった。このことから、本発明において、プライマーコート層を塩素化ポリオレフィン系樹脂とすることは、不連続な金属被膜を剥がれ難くするのに効果があるのがわかる。   The results are as shown in Table 2. In Example 2 in which the primer paint was a chlorinated polyolefin resin, 100% of the primer was not peeled off (100/100), whereas the primer paint was an acrylic resin. Comparative Example 5 in which the coating material was used and Comparative Example 6 in which the primer coating material was used as the polyurethane-based resin both resulted in 100% peeling of 100% (100/100). From this, it can be seen that, in the present invention, using a chlorinated polyolefin resin as the primer coat layer is effective in making it difficult to peel off the discontinuous metal film.

Figure 2012183784
Figure 2012183784

本発明において、パーオキサイド架橋によるシリコーンゴムによる不連続な金属被膜との密着性(剥離し難さ)が良好である理由は定かではないが、ゴム中のパーオキサイド残渣によるものと考えられる。架橋前のシリコーンの側鎖はメチル基やビニル基等からなり、ビニル基は2〜30%程度含まれているため、メチル基とビニル基間の架橋がおきる。当該架橋の場合、ラジカルは消費されず、架橋後に温度が下がればパーオキサイドに戻るため、ゴム中にパーオキサイドが残存すると考えられる。パーオキサイド残渣をフレーム処理等することで、パーオキサイドが再度分解してラジカルが発生し、その状態で塩素化ポリオレフィン系樹脂プライマーが塗布されることにより、シリコーン表面のメチル基やビニル基等と、プレイマー中の炭化水素鎖や炭化水素基等とが架橋して、接着性が向上すると考えられる。すなわち、フレーム処理等によって、表面極性を発生させることで密着性を向上すると共に、シリコーン中にラジカルを発生させて、シリコーンとプライマーとを架橋をさせる効果によりさらに密着力が向上すると考えられる。   In the present invention, the reason why the adhesion (difficult to peel off) with the discontinuous metal film by the silicone rubber by peroxide crosslinking is good is not clear, but it is thought to be due to the peroxide residue in the rubber. The side chain of the silicone before cross-linking consists of a methyl group, a vinyl group, etc., and the vinyl group is contained in an amount of about 2 to 30%. In the case of the cross-linking, radicals are not consumed, and if the temperature drops after cross-linking, the peroxide returns to the peroxide, so it is considered that the peroxide remains in the rubber. By subjecting the peroxide residue to flame treatment etc., the peroxide is decomposed again to generate radicals, and by applying a chlorinated polyolefin resin primer in that state, the silicone surface methyl group, vinyl group, etc., It is considered that the hydrocarbon chains and hydrocarbon groups in the premer are cross-linked and the adhesion is improved. That is, it is considered that the adhesion is further improved by the effect of cross-linking the silicone and the primer by generating radicals in the silicone while generating the surface polarity by frame treatment or the like.

このように、本発明品は、金属被膜が基材から剥がれ難く、しかも変色や変形が無く、美観の良好な金属調を有するものであり、例えば、自動車の内装、外装部材、スイッチ、センターパネル周りの加飾部品、クッション部材等に好適なものである。
なお、前記の実施例では、基材の片面のみに金属被膜を形成したが、基材の両面に金属被膜を形成してもよい。
As described above, the product of the present invention is such that the metal coating is difficult to peel off from the base material, has no discoloration or deformation, and has a good metallic appearance. For example, an automobile interior, exterior member, switch, center panel It is suitable for surrounding decorative parts, cushion members and the like.
In addition, in the said Example, although the metal film was formed only on the single side | surface of a base material, you may form a metal film on both surfaces of a base material.

10 金属被膜を有する弾性体
11 基材
13 プライマーコート層
15 アンダーコート層
21 不連続な金属被膜
25 トップコート層
DESCRIPTION OF SYMBOLS 10 Elastic body which has metal film 11 Base material 13 Primer coat layer 15 Undercoat layer 21 Discontinuous metal film 25 Topcoat layer

Claims (3)

パーオキサイド架橋により形成され、D4〜D10の低分子シロキサンの含有量が300PPM以下であるシリコーン基材上に、塩素化ポリオレフィン系樹脂からなるプライマーコート層と、アクリル系樹脂又はポリウレタン系樹脂からなるアンダーコート層と、蒸着により形成された不連続な金属被膜と、トップコート層がこの順に積層され、前記トップコート層が前記アンダーコート層と同材料からなることを特徴とする不連続な金属被膜を有する弾性体。   A primer coat layer made of a chlorinated polyolefin resin and an undercoat made of an acrylic resin or a polyurethane resin on a silicone substrate formed by peroxide crosslinking and having a content of low molecular siloxanes of D4 to D10 of 300 PPM or less A discontinuous metal coating comprising: a coat layer; a discontinuous metal film formed by vapor deposition; and a top coat layer laminated in this order; and the top coat layer is made of the same material as the undercoat layer. Elastic body having. パーオキサイド架橋により形成されるシリコーンゴムからなる基材に蒸着された不連続な金属被膜を有する弾性体の製造方法であって、 前記基材を180〜200℃で1〜12時間加熱処理した後、 前記基材表面にフレーム処理、コロナ放電処理、プラズマ処理の群から一つ選択される表面処理を施し、 前記基材の表面に塩素化ポリオレフィン系樹脂からなるプライマーコート層とアンダーコート層を順に形成した後、 蒸着により不連続な金属被膜を形成し、 前記不連続な金属被膜上に前記アンダーコート層と同材料からなるトップコート層を形成することを特徴とする不連続な金属被膜を有する弾性体の製造方法。 A method for producing an elastic body having a discontinuous metal film deposited on a base material made of silicone rubber formed by peroxide crosslinking, wherein the base material is heated at 180 to 200 ° C for 1 to 12 hours. The substrate surface is subjected to a surface treatment selected from the group of flame treatment, corona discharge treatment and plasma treatment, and a primer coat layer and an undercoat layer made of a chlorinated polyolefin resin are sequentially applied to the surface of the substrate. After forming, a discontinuous metal film is formed by vapor deposition, and a topcoat layer made of the same material as the undercoat layer is formed on the discontinuous metal film. A method for producing an elastic body. 前記プライマーコート層は塩素化ポリオレフィン系樹脂からなり、前記アンダーコート層とトップコート層はアクリル系樹脂又はポリウレタン系樹脂からなることを特徴とする請求項2に記載の不連続な金属被膜を有する弾性体の製造方法。
The elasticity having a discontinuous metal coating according to claim 2, wherein the primer coat layer is made of a chlorinated polyolefin resin, and the undercoat layer and the top coat layer are made of an acrylic resin or a polyurethane resin. Body manufacturing method.
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JP2016182675A (en) * 2015-03-25 2016-10-20 帝人コードレ株式会社 Metal thin film decorative sheet-like matter and method for producing the same

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JP2000077891A (en) * 1998-09-01 2000-03-14 Ge Toshiba Silicones Co Ltd Flexible metallic layer-juxtaposing silicone rubber material
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JPS62115065A (en) * 1985-11-14 1987-05-26 Toyoda Gosei Co Ltd Bondable composition
JPH09509194A (en) * 1994-01-11 1997-09-16 ロード コーポレーション Topcoat and adhesive compositions based on chlorinated polyolefin with high chlorine content
JP2000077891A (en) * 1998-09-01 2000-03-14 Ge Toshiba Silicones Co Ltd Flexible metallic layer-juxtaposing silicone rubber material
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2016182675A (en) * 2015-03-25 2016-10-20 帝人コードレ株式会社 Metal thin film decorative sheet-like matter and method for producing the same

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