JPS61281133A - Composition for coating surface - Google Patents

Composition for coating surface

Info

Publication number
JPS61281133A
JPS61281133A JP60122170A JP12217085A JPS61281133A JP S61281133 A JPS61281133 A JP S61281133A JP 60122170 A JP60122170 A JP 60122170A JP 12217085 A JP12217085 A JP 12217085A JP S61281133 A JPS61281133 A JP S61281133A
Authority
JP
Japan
Prior art keywords
acrylic resin
resin
composition
curing agent
alumina
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP60122170A
Other languages
Japanese (ja)
Inventor
Hideo Nakamoto
中本 英夫
Yoshihisa Osaka
大坂 宣久
Kinuko Suzuki
鈴木 衣子
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsubishi Rayon Co Ltd
Original Assignee
Mitsubishi Rayon Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Mitsubishi Rayon Co Ltd filed Critical Mitsubishi Rayon Co Ltd
Priority to JP60122170A priority Critical patent/JPS61281133A/en
Publication of JPS61281133A publication Critical patent/JPS61281133A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
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Abstract

PURPOSE:The titled composition, containing a specific acrylic resin, curing agent and alpha-alumina particles in a solvent, capable of forming films having high hardness and improved smoothness, adhesion, etc., and suitable for coating thermoplastics. CONSTITUTION:A composition obtained by incorporating (A) an acrylic resin having >=30 deg.C glass transition temperature and 20-120 hydroxyl value, (B) a curing agent for the component (A), e.g. amino resin or polyisocyanate compound and (C) 35-85wt%, based on the total solid content in the composition, particulate alpha-alumina having 5-50mum average particle diameter in a solvent, e.g. toluene or xylene.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は改良された表面被覆用組成物に関し、特にAB
S樹脂、ポリカーボネート樹脂等の熱可塑性プラスチッ
クのコーティングに適した表面被覆用組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field] The present invention relates to improved surface coating compositions, particularly AB
The present invention relates to a surface coating composition suitable for coating thermoplastic plastics such as S resin and polycarbonate resin.

〔発明の概要〕[Summary of the invention]

本発明は、表面被覆用組成物において、溶剤中に特定の
ガラス転移温度及び特定のヒドロキシル価を有するアク
リル樹脂、該アクリル樹脂の硬化剤及び特定のα−アル
ミナ粒子とを主剤として含有することにより、 高硬度で優れた耐摩耗性を有すると共に、平滑性、密着
性及び耐薬品性の緒特性にも優れている被膜を形成し得
ることができるようにしたものである。
The present invention provides a surface coating composition containing as a main ingredient an acrylic resin having a specific glass transition temperature and a specific hydroxyl value, a curing agent for the acrylic resin, and specific α-alumina particles. It is possible to form a coating having high hardness and excellent abrasion resistance, as well as excellent smoothness, adhesion, and chemical resistance.

〔従来の技術〕[Conventional technology]

近年、弱電分野並びに機械部品分野において、金属部材
に替わってABS樹脂、ポリカーボネート樹脂等の熱可
塑性プラスチック成型品の使用される比率が高まるにつ
れ、これらの材料の耐摩耗性、耐擦傷性等表面耐久性の
向上が望まれている。
In recent years, as the proportion of thermoplastic molded products such as ABS resin and polycarbonate resin being used instead of metal parts in the fields of light electrical appliances and mechanical parts has increased, the surface durability such as wear resistance and scratch resistance of these materials has increased. There is a desire for improvement in sexual performance.

従来、金属材料や木質系床材の耐久性を向上させる方法
として、(1)酸硬化型アミノアルキッド樹脂固形分又
は湿気硬化型ポリウレタン樹脂固形分に対して酸化アル
ミニウムを主成分とする鉱物質物質を0.5〜30重量
%及び繊維質物質を1〜50重量%分散含有させた組成
物(特公昭51−35487号)、(2)ウレタン樹脂
100重量部に対してα−アルミナを5〜7.5重量部
と炭化ケイ素を2.5〜5.0重量部配合した組成物(
特公昭55−33475号)、(3)耐摩耗性を有する
熱可塑性樹脂に硬度の高いセラミックスを混合分散させ
た組成物(特開昭54−4930号)等の耐摩耗性コー
テイング材による表面被覆用処理方法が提案されている
Conventionally, as a method to improve the durability of metal materials and wood-based flooring materials, (1) mineral substances mainly composed of aluminum oxide were added to the solid content of acid-curing amino alkyd resin or moisture-curing polyurethane resin; (Japanese Patent Publication No. 51-35487), (2) 5 to 30 parts by weight of α-alumina per 100 parts by weight of urethane resin. A composition containing 7.5 parts by weight and 2.5 to 5.0 parts by weight of silicon carbide (
(3) surface coating with a wear-resistant coating material such as a composition in which hard ceramics are mixed and dispersed in a wear-resistant thermoplastic resin (Japanese Patent Publication No. 54-4930); A treatment method has been proposed.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

しかし、前記(1)及び(2)の方法は床材の耐久性を
向上させる方法であって、熱可塑性プラスチック成型品
の表面耐久性を付与することが困難であるばかりでなく
、該成型品に対する密着性も不十分である。
However, methods (1) and (2) above are methods for improving the durability of flooring materials, and it is not only difficult to impart surface durability to thermoplastic molded products, but also The adhesion to is also insufficient.

また、前記(3)の方法の耐摩耗性を有する熱可塑性樹
脂、例えばナイロン、ポリアセクール、テフロン等は通
常の溶剤に溶解させることが難しく、作業性の良好な耐
摩耗性コーテイング材を製造することが困難であるとい
う問題がある。
Furthermore, it is difficult to dissolve the abrasion-resistant thermoplastic resins used in method (3), such as nylon, polyacecool, Teflon, etc. in ordinary solvents, and it is therefore difficult to produce an abrasion-resistant coating material with good workability. The problem is that it is difficult.

本発明の目的は、高硬度で優れた耐摩耗性を有している
と共に、平滑性、密着性及び耐薬品性等の緒特性にも優
れている皮膜を形成し得る表面被覆用組成物を提供する
ことにある。
The object of the present invention is to provide a surface coating composition that can form a film that has high hardness and excellent wear resistance, and also has excellent properties such as smoothness, adhesion, and chemical resistance. It is about providing.

また本発明の他の目的は耐摩耗性、耐擦傷性等の表面特
性に優れた皮膜を形成し得るため、特にABS樹脂、ポ
リカーボネート樹脂等の熱可塑性プラスチック成型品の
コーティングに好適に用いることのできる表面被覆用組
成物を提供することにある。
Another object of the present invention is to form a film with excellent surface properties such as abrasion resistance and scratch resistance, so that it can be used particularly for coating thermoplastic molded products such as ABS resin and polycarbonate resin. The object of the present invention is to provide a surface coating composition that can be used for surface coating.

〔問題点を解決するための手段〕[Means for solving problems]

前記の目的を達成するため、本発明者等は、α−アルミ
ナと熱可塑性樹脂との種々の組合せに関して鋭意研究の
結果、本発明を完成させるに至った。即ち、本発明は溶
剤中にガラス転移温度が30℃以上でかつヒドロキシル
価が20〜120であるアクリル樹脂、該アクリル樹脂
の硬化剤及び球状α−アルミナを主剤として含有するこ
とを特徴とする表面被覆用組成物である。
In order to achieve the above object, the present inventors conducted intensive research on various combinations of α-alumina and thermoplastic resin, and as a result, completed the present invention. That is, the present invention provides a surface characterized by containing an acrylic resin having a glass transition temperature of 30° C. or higher and a hydroxyl value of 20 to 120, a curing agent for the acrylic resin, and spherical α-alumina as main ingredients in a solvent. It is a coating composition.

本発明で使用するアクリル樹脂はガラス転移温度が30
℃以上でかつヒドロキシル価が20〜120であるアク
リル樹脂であればよい。ガラス転移温度が30℃未満と
なると、得られる塗膜の耐摩耗性、耐擦傷性が著しく低
下するばかりでなく、耐汚染性、耐候性も悪化するので
好ましくない。また、アクリル樹脂のヒドロキシル価が
20未満となると、得られる塗膜の耐溶剤性、表面硬度
、耐摩耗性が低下し、120を超えるものを使用すると
、塗装作業性、密着性、耐候性が悪化するので好ましく
ない。
The acrylic resin used in the present invention has a glass transition temperature of 30
Any acrylic resin having a temperature of 20 to 120 and a hydroxyl value of 20 to 120 may be used. If the glass transition temperature is less than 30°C, it is not preferable because not only the abrasion resistance and scratch resistance of the resulting coating film are significantly reduced, but also the stain resistance and weather resistance are deteriorated. In addition, if the hydroxyl value of the acrylic resin is less than 20, the solvent resistance, surface hardness, and abrasion resistance of the resulting coating film will decrease, and if it exceeds 120, the coating workability, adhesion, and weather resistance will decrease. This is not desirable as it will make things worse.

該アクリル樹脂は、(メタ)アクリル酸2−ヒドロキシ
エチルエステル、(メタ)アクリル酸2−ヒドロキシプ
ロピルエステル、(メタ)アクリル酸4−ヒドロキシブ
チルエステル等のヒドロキシル基含有モノマー及びヒド
ロキシル基を含まない(メタ)アクリル酸アルキルエス
テルを必須成分とするモノマー混合物、或いは該必須成
分と、該必須成分と共重合可能なビニルモノマー、例え
ばスチレン、ビニルトルエン、酢酸ビニル、アクリロニ
トリル、メタクリル酸、アクリル酸、イタコン酸等、又
はこれらの混合物とを含むモノマー混合物を通常の方法
で重合して得られる樹脂である。なお前記において(メ
タ)アクリル酸とあるのはアクリル酸とメタクリル酸の
いずれか一方を示す。
The acrylic resin contains hydroxyl group-containing monomers such as (meth)acrylic acid 2-hydroxyethyl ester, (meth)acrylic acid 2-hydroxypropyl ester, (meth)acrylic acid 4-hydroxybutyl ester, and hydroxyl group-free ( A monomer mixture containing meth)acrylic acid alkyl ester as an essential component, or a vinyl monomer copolymerizable with the essential component, such as styrene, vinyltoluene, vinyl acetate, acrylonitrile, methacrylic acid, acrylic acid, itaconic acid It is a resin obtained by polymerizing a monomer mixture containing the same or a mixture thereof using a conventional method. Note that (meth)acrylic acid in the above refers to either acrylic acid or methacrylic acid.

本発明で使用されるアクリル樹脂の硬化剤は、特に制限
されず、ヒドロキシル基含有重合体と反応しうる従来公
知の硬化剤のうちから適宜選択使用することができ、例
えばメチルエーテル化メラミン樹脂、ブチルエーテル化
メラミン樹脂、ブチルエーテル化ベンゾグアナミン樹脂
及びブチルエーテル化尿素樹脂で代表されるアミノ樹脂
;1分子中にイソシアネート基を少なくとも2個以上有
するポリイソシアネート化合物;1分子中に酸無水物基
を2個以上有する化合物又は樹脂;1分子中にアルコキ
シシラン基を2個以上有するシリコーン素樹脂;等があ
げられるが、なかでも特にアミノ樹脂とポリイソシアネ
ート化合物が耐摩耗性コーテイング材として顕著な効果
を発揮するので好ましく使用される。硬化剤の配合量は
、硬化反応性基の量等を考慮して樹脂及び硬化剤の組合
せに応じて適宜法めることにより、皮膜の性状をコント
ロールすることができる。通常は、アクリル樹脂中の反
応性基の量に対して硬化剤中の反応性基の量を当量ある
いはそれ以下の量とする割合で配合される。
The curing agent for the acrylic resin used in the present invention is not particularly limited, and can be appropriately selected from conventionally known curing agents that can react with hydroxyl group-containing polymers, such as methyl etherified melamine resin, Amino resins represented by butyl etherified melamine resins, butyl etherified benzoguanamine resins, and butyl etherified urea resins; polyisocyanate compounds having at least two isocyanate groups in one molecule; two or more acid anhydride groups in one molecule Compounds or resins; silicone base resins having two or more alkoxysilane groups in one molecule; etc., among which amino resins and polyisocyanate compounds are particularly preferred as they exhibit remarkable effects as wear-resistant coating materials. used. The properties of the film can be controlled by adjusting the amount of the curing agent as appropriate depending on the combination of resin and curing agent, taking into consideration the amount of curing reactive groups and the like. Usually, the amount of reactive groups in the curing agent is equivalent to or less than the amount of reactive groups in the acrylic resin.

本発明で使用する球状α−アルミナ粒子の原料又は製造
過程は特に制限されないが、例えば中間体としてのT−
アルミナを用い直接α−アルミナ球状体として製造され
たもの、又はα−アルミナの微細焼結体を粉砕し、再焼
結して得られる良質の粒状粒子などが好ましく使用され
る。
The raw material or manufacturing process for the spherical α-alumina particles used in the present invention is not particularly limited, but for example, T-
Preferably used are those produced directly as α-alumina spheres using alumina, or high-quality granular particles obtained by crushing and resintering a fine sintered body of α-alumina.

次に、使用する球状α−アルミナ粒子の粒径については
平均粒径が5〜50μmの範囲が最も優れた耐摩耗性を
与える。即ち50I1mを超えると摩擦子による摺動過
程において、摩擦摺動が粒子を捕獲し、樹脂層から離脱
し易くなり、また逆に5μm未満であるとアクリル樹脂
と挙動を共にし易くなり、樹脂特性の影響が大きく、球
状効果が消失する方向にある。尚、球状α−アルミナの
真球度に関しては全部の粒子が真球形状であることに越
したことはないが、α−アルミナ粒子は約半数が球状で
あれば充分その特性を発揮する。
Next, regarding the particle size of the spherical α-alumina particles used, the average particle size in the range of 5 to 50 μm provides the best wear resistance. In other words, if it exceeds 50I1m, the frictional sliding will capture particles during the sliding process by the friction element, and they will easily separate from the resin layer.On the other hand, if it is less than 5μm, they will tend to behave in the same way as the acrylic resin, which will affect the resin properties. has a large influence, and the spherical effect tends to disappear. Regarding the sphericity of spherical α-alumina, it is best if all the particles are perfectly spherical, but α-alumina particles sufficiently exhibit their characteristics if about half of them are spherical.

球状α−アルミナ粒子の配合量は、表面被覆用組成物の
全固形分に対して35〜85重景%で重量ことが好まし
く、35重量%未満では、耐摩耗性ならびに耐擦傷性が
極端に低下し、また85重量%を超えると、塗装作業性
の低下を招くばかりでなく、前述のような熱可塑性プラ
スチック等の基材に対する密着性の低下をも招くので好
ましくない。
The blending amount of the spherical α-alumina particles is preferably 35 to 85% by weight based on the total solid content of the surface coating composition, and if it is less than 35% by weight, the abrasion resistance and scratch resistance will be extremely poor. Moreover, if it exceeds 85% by weight, it is not preferable because it not only causes a decrease in painting workability but also causes a decrease in adhesion to substrates such as thermoplastic plastics as described above.

本発明で使用する溶剤は被覆される表面の溶剤劣化を来
さないものであれば、特に制限されるものではなく、例
としてトルエン、キシレン等の炭化水素類、酢酸エチル
、酢酸ブチル等のエステル類、及びメチルエチルケトン
、メチルイソブチルケトン等のケトン類が挙げられる。
The solvent used in the present invention is not particularly limited as long as it does not cause deterioration of the surface to be coated. Examples include hydrocarbons such as toluene and xylene, and esters such as ethyl acetate and butyl acetate. and ketones such as methyl ethyl ketone and methyl isobutyl ketone.

本発明の表面被覆用組成物を使用する際には、前記アク
リル樹脂、硬化剤、球状α−アルミナ粒子及び希釈溶剤
を所定量配合し、スプレー塗装、ロールコータ−塗装等
の方法で塗布し、然る後に塗膜を乾燥して強固な皮膜を
得る。
When using the surface coating composition of the present invention, a predetermined amount of the acrylic resin, curing agent, spherical α-alumina particles, and diluting solvent are blended, and the composition is applied by spray coating, roll coater coating, etc. After that, the coating film is dried to obtain a strong film.

組成物の配合に際しては本発明の効果を損なわない範囲
で通常使用される添加剤、着色剤、顔料、熱可塑性樹脂
及び溶剤等を添加して使用することもできる。
When formulating the composition, commonly used additives, colorants, pigments, thermoplastic resins, solvents, etc. may be added to the extent that they do not impair the effects of the present invention.

〔発明の効果〕 本発明によれば、アクリル樹脂のガラス転移温度を30
°C以上及びヒドロキシル価を20〜120と規定し、
かつα−アルミナ粒子の形状を球状と規定することによ
り、溶剤中にこれら2成分及び前記アクリル樹脂用の硬
化剤を主剤として含有する表面被覆用組成物は、従来の
耐摩耗性コーテイング材に比べて優れた耐久性を熱可塑
性プラスチック成型品の表面に付与することができかつ
塗装作業性も良好である。
[Effects of the Invention] According to the present invention, the glass transition temperature of the acrylic resin is reduced to 30
°C or higher and the hydroxyl number is defined as 20 to 120,
In addition, by defining the shape of the α-alumina particles as spherical, a surface coating composition containing these two components and the curing agent for the acrylic resin as main ingredients in a solvent can be used as a surface coating composition compared to conventional wear-resistant coating materials. It is possible to impart excellent durability to the surface of thermoplastic molded products, and the coating workability is also good.

〔実施例〕〔Example〕

以下実施例により本発明を具体的に説明する。 The present invention will be specifically explained below using Examples.

なお、実施例中「部」とあるのは重量部、「%」とある
のは重量%を意味する。
In the examples, "part" means part by weight, and "%" means weight %.

(実施例1〜3) 第1表に示した重合用上ツマー組成によりトルエン中で
アゾビスイソブチロニトリルを重合開始剤に用いて80
℃で重合を行うことによって、ガラス転移温度とヒドロ
キシル価の異なるアクリル樹脂のトルエン溶液を得た。
(Examples 1 to 3) Using azobisisobutyronitrile as a polymerization initiator in toluene according to the polymerization composition shown in Table 1,
By polymerizing at ℃, toluene solutions of acrylic resins with different glass transition temperatures and hydroxyl values were obtained.

このアクリル樹脂溶液にポリイソシアネート化合物であ
るタケネートD−11ON (武田薬品工業株式会社製
)をアクリル樹脂中のヒドロキシ基量と当量となるよう
に添加した後、粒子径10μmの球状α−アルミナを固
形分換算で50%、70%及び80%となるように加え
高速攪拌を行うことによってそれぞれコーテイング材(
I)、(II)及び(Ill)を得た。
After adding Takenate D-11ON (manufactured by Takeda Pharmaceutical Co., Ltd.), a polyisocyanate compound, to this acrylic resin solution in an amount equivalent to the amount of hydroxyl groups in the acrylic resin, spherical α-alumina with a particle size of 10 μm was solidified. The coating material (
I), (II) and (Ill) were obtained.

こうして得た各コーテイング材をABS樹脂板に30μ
mとなるようにスプレー塗装し、60℃で60分間乾燥
を行った。この方法により得た塗装板の塗膜性能評価結
果を第1表に示す。この結果から、本発明の耐摩耗性コ
ーテイング材は極めて良好な耐摩耗性及び耐擦傷性を示
すことが明らかである。
Each coating material obtained in this way was applied to an ABS resin plate with a thickness of 30 μm.
It was spray-painted so that it became m, and it dried at 60 degreeC for 60 minutes. Table 1 shows the results of evaluating the coating film performance of the coated plates obtained by this method. From this result, it is clear that the wear-resistant coating material of the present invention exhibits extremely good wear resistance and scratch resistance.

(比較例1と2) 比較のため、第1表に示した如くガラス転移温度とヒド
ロキシル価の異なるアクリル樹脂を用いる他は実施例1
と全く同じ条件で塗料化を行い、コーテイング材(IV
)と(V)を得た。このコーテイング材を用いて実施例
1と同じ条件で塗装板を作製し、性能評価を実施した。
(Comparative Examples 1 and 2) For comparison, Example 1 was used except that acrylic resins with different glass transition temperatures and hydroxyl values were used as shown in Table 1.
The coating material (IV
) and (V) were obtained. A coated plate was prepared using this coating material under the same conditions as in Example 1, and performance evaluation was performed.

結果を第1表に示す。The results are shown in Table 1.

(実施例4) 実施例2のコーテイング材(n)で使用したアクリル樹
脂のトルエンと酢酸エチル混合溶剤溶液にブチルエーテ
ル化メラミン樹脂(商品名ユーバゾ:)22R,三井東
圧化学株式会社製)を固形分比でアクリル樹脂/メラミ
ン樹脂=70/30(重量比)となるように混合溶解し
た後、粒子径10μmの球状α−アルミナを固形分換算
で65%となるように添加し、高速攪拌を行うことによ
って、コーテイング材(Vl)を得た。
(Example 4) Butyl etherified melamine resin (trade name Yubazo: 22R, manufactured by Mitsui Toatsu Chemical Co., Ltd.) was solidified in a mixed solvent solution of toluene and ethyl acetate of the acrylic resin used in the coating material (n) of Example 2. After mixing and dissolving the acrylic resin/melamine resin in a ratio of 70/30 (weight ratio), spherical α-alumina with a particle size of 10 μm was added to give a solid content of 65%, and the mixture was stirred at high speed. By doing so, a coating material (Vl) was obtained.

こうして得たコーテイング材(Vl)を、ポリカーボネ
ート樹脂、ノリル樹脂、ナイロン樹脂の各成型品に塗装
し、各々を110℃で60分間乾燥した。得られた塗装
物品は優れた密着性、耐摩耗性、耐擦傷性を示すことが
認められた。
The coating material (Vl) thus obtained was applied to each molded product of polycarbonate resin, noryl resin, and nylon resin, and each molded product was dried at 110° C. for 60 minutes. It was observed that the obtained coated article exhibited excellent adhesion, abrasion resistance, and scratch resistance.

(以下、余白次頁につづく)(Continued below in the margin on the next page)

Claims (1)

【特許請求の範囲】 1、溶剤中にガラス転移温度が30℃以上でかつヒドロ
キシル価が20〜120であるアクリル樹脂、該アクリ
ル樹脂の硬化剤及び球状α−アルミナを主剤として含有
することを特徴とする表面被覆用組成物。 2、アクリル樹脂の硬化剤がアミノ樹脂である特許請求
の範囲第1項記載の表面被覆用組成物。 3、アクリル樹脂の硬化剤がポリイソシアネート化合物
である特許請求の範囲第1項記載の表面被覆用組成物。 4、球状α−アルミナ粒子の配合量が、表面被覆用組成
物の全固形分に対して35〜85重量%である特許請求
の範囲第1項〜第3項のいずれか1項に記載の表面被覆
用組成物。
[Claims] 1. The solvent contains an acrylic resin having a glass transition temperature of 30° C. or higher and a hydroxyl value of 20 to 120, a curing agent for the acrylic resin, and spherical α-alumina as main ingredients. A composition for surface coating. 2. The surface coating composition according to claim 1, wherein the curing agent for the acrylic resin is an amino resin. 3. The surface coating composition according to claim 1, wherein the curing agent for the acrylic resin is a polyisocyanate compound. 4. According to any one of claims 1 to 3, the amount of the spherical α-alumina particles is 35 to 85% by weight based on the total solid content of the surface coating composition. Composition for surface coating.
JP60122170A 1985-06-05 1985-06-05 Composition for coating surface Pending JPS61281133A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60122170A JPS61281133A (en) 1985-06-05 1985-06-05 Composition for coating surface

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60122170A JPS61281133A (en) 1985-06-05 1985-06-05 Composition for coating surface

Publications (1)

Publication Number Publication Date
JPS61281133A true JPS61281133A (en) 1986-12-11

Family

ID=14829308

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60122170A Pending JPS61281133A (en) 1985-06-05 1985-06-05 Composition for coating surface

Country Status (1)

Country Link
JP (1) JPS61281133A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5340781A (en) * 1986-07-14 1994-08-23 Showa Denko Kabushiki Kaisha Spherical corundum particles, process for preparation thereof and rubber or plastic composition having high thermal conductivity and having spherical corundum paticles incorporated therein
JP2001055542A (en) * 1999-08-19 2001-02-27 Masami Soki Modification of synthetic resin for surface coating
WO2018096976A1 (en) * 2016-11-25 2018-05-31 リケンテクノス株式会社 Coating material for formation of matte hard coat, and decorative sheet using same

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5340781A (en) * 1986-07-14 1994-08-23 Showa Denko Kabushiki Kaisha Spherical corundum particles, process for preparation thereof and rubber or plastic composition having high thermal conductivity and having spherical corundum paticles incorporated therein
JP2001055542A (en) * 1999-08-19 2001-02-27 Masami Soki Modification of synthetic resin for surface coating
WO2018096976A1 (en) * 2016-11-25 2018-05-31 リケンテクノス株式会社 Coating material for formation of matte hard coat, and decorative sheet using same
JPWO2018096976A1 (en) * 2016-11-25 2019-10-17 リケンテクノス株式会社 Matte hard coat forming paint and decorative sheet using the same
US11466111B2 (en) 2016-11-25 2022-10-11 Riken Technos Corporation Coating material for formation of matte hard coat, and decorative sheet using same

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