JPS59223746A - Phenolic resin molding material for substrate to be plated - Google Patents
Phenolic resin molding material for substrate to be platedInfo
- Publication number
- JPS59223746A JPS59223746A JP9821783A JP9821783A JPS59223746A JP S59223746 A JPS59223746 A JP S59223746A JP 9821783 A JP9821783 A JP 9821783A JP 9821783 A JP9821783 A JP 9821783A JP S59223746 A JPS59223746 A JP S59223746A
- Authority
- JP
- Japan
- Prior art keywords
- phenolic resin
- molding material
- rubber
- substrate
- parts
- 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
Links
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
- Electroplating Methods And Accessories (AREA)
- Conductive Materials (AREA)
Abstract
Description
【発明の詳細な説明】
〔技術分野〕
本発明は配線器具、電気器具、家庭用品等に用いるフェ
ノール樹脂成形材料に関するもので、特に化学銭金を必
要としない成形品を得るフェノール樹脂成形材料に関す
るものである。[Detailed Description of the Invention] [Technical Field] The present invention relates to a phenolic resin molding material used for wiring devices, electrical appliances, household goods, etc., and particularly relates to a phenolic resin molding material for producing molded products that do not require chemical money. It is something.
従来、フェノール樹脂成形品に鍍金を施すには、成形品
を脱脂、予備エツチング、エツチング、中和、化学鍍金
、電気鍍金という工程を必要としていたがその工程は長
くコスト上昇の原因となっていた。Conventionally, plating phenolic resin molded products required the following steps: degreasing the molded product, pre-etching, etching, neutralization, chemical plating, and electroplating, but these processes were long and caused increased costs. .
不発明の目的とするところは化学鍍金工程を省略し直ち
に電気銭金ができるようにすることにある。The purpose of the invention is to omit the chemical plating process and to immediately produce electric money.
不発明は導電性材料とコムを添加し成形品の体積抵抗率
がlOΩO7+以下になるようにしたフェノール樹脂成
形月別であるため成形品に直接、電気銭金を施すことが
できるようになったものである。The invention was made by molding a phenolic resin by adding conductive materials and combs so that the volume resistivity of the molded product was less than 1OΩO7+, which made it possible to apply electrical money directly to the molded product. It is.
以下本発明の詳細な説明する。本発明に用いるフェノー
ル樹脂はフェノール、クレゾール、キシレノール等のフ
ェノール類又は糖瓜、リク゛ニン、キシレン、ナフタリ
ン、石油系芳香族炭化水素等による変性フェノール類と
ホルマリン、バラホルムアルデヒド等のアルデヒド類と
を所定のモル比に配合し1塩酸、硫酸、蓚酸のような酸
性触媒下で反応させたノボラック型フェノール樹脂又は
水酸化ナトリウム、アンモニア、アミン等のアルカリ性
触媒下で反応させたレゾール型フェノール樹脂である。The present invention will be explained in detail below. The phenolic resin used in the present invention is a mixture of phenols such as phenol, cresol, and xylenol, or phenols modified with sugar melon, liqunin, xylene, naphthalene, petroleum aromatic hydrocarbons, etc., and aldehydes such as formalin and formaldehyde. Novolac type phenol resins are mixed in a molar ratio of 1 to 1 and reacted under an acidic catalyst such as hydrochloric acid, sulfuric acid, or oxalic acid, or resol type phenolic resins are reacted under an alkaline catalyst such as sodium hydroxide, ammonia, or amine.
ノボラック型フェノール樹脂を用いる場合は硬化剤とし
てヘキサメチレンテトラミンを樹脂に対して6〜20重
量%(以下単に%と記す)添加する。充填剤としては木
粉、炭酸カルシウム、パルプ、シリカ等の有機、無機充
填剤が用いられ、離型剤としてはステアリン酸、ワック
ス、金属石鹸等が用いられる。導電性材料としては金属
粉、金属箔、金属片、カーボンブラック、黒鉛等が用い
られる。導電性材料の添加量は充填剤の種類、添加量等
によって変更するが成形品の体積抵抗率が10Ω副以下
になるように添加することが必要である。即ち体積抵抗
率が1♂Ω口をこえると成形品に直接電気鍍金すること
が不可能になるからである。成形品と鍍金層との密着性
を向上させるために添加するゴムとしてはスチレンゴム
、ブチルゴム、イーンプレンゴム、ニトリルゴム、クロ
ロプレンゴム等が用いられるが好ましくはフェノール樹
脂との相溶性に優れるニトリルゴムを全量に対し3〜1
0%添加することが望ましい。即ち3%未満では成形品
と鍍金層との密着性が小さくなる傾向にあり、10%を
こえると剛性が低下する傾向に 。When using a novolak type phenol resin, 6 to 20% by weight (hereinafter simply referred to as %) of hexamethylenetetramine is added to the resin as a curing agent. Organic or inorganic fillers such as wood flour, calcium carbonate, pulp, and silica are used as fillers, and stearic acid, wax, metal soap, etc. are used as release agents. As the conductive material, metal powder, metal foil, metal piece, carbon black, graphite, etc. are used. The amount of conductive material added varies depending on the type of filler, the amount added, etc., but it must be added so that the volume resistivity of the molded product is 10Ω or less. That is, if the volume resistivity exceeds 1♂Ω, it becomes impossible to directly electroplate the molded product. As the rubber added to improve the adhesion between the molded product and the plating layer, styrene rubber, butyl rubber, inprene rubber, nitrile rubber, chloroprene rubber, etc. are used, but nitrile rubber is preferable because it has excellent compatibility with phenolic resin. 3 to 1 for the total amount
It is desirable to add 0%. That is, if it is less than 3%, the adhesion between the molded product and the plating layer tends to decrease, and if it exceeds 10%, the rigidity tends to decrease.
あるからである。かくしてこれらフェノール樹脂、硬化
剤、導電性材料、ゴム、充填剤、離型剤、着色剤等を混
合、混線、粉砕して献金素地用フェノール樹脂成形材料
を得るものである。Because there is. The phenolic resin, curing agent, conductive material, rubber, filler, mold release agent, coloring agent, etc. are thus mixed, mixed, and pulverized to obtain a phenolic resin molding material for the donor base.
以下本発明を実施例にもとすいて説明する。The present invention will be explained below using examples.
実施例1
軟化点90℃ のノボラック型フェノール樹脂40重量
S(以下単に部と記す)に対しヘキサメチレンテトラミ
ン8部、ステアリン酸2部、カーボンブラック2部、3
0メツシユのアルミニウム箔10部、ニトリルゴム3部
、重質炭酸カルシウム35部を加え、混合、混線、粉砕
して鍍金素地用フェノール樹脂成形材料を得た。Example 1 8 parts of hexamethylenetetramine, 2 parts of stearic acid, 2 parts of carbon black, 3 parts of novolak type phenolic resin with a softening point of 90° C.
10 parts of aluminum foil of 0 mesh, 3 parts of nitrile rubber, and 35 parts of heavy calcium carbonate were added, mixed, mixed, and crushed to obtain a phenolic resin molding material for plating base.
実施例2
実施例1と同じフェノール樹脂40都に対し、ヘキサメ
チレンテトラミン8部、ステアリン酸2部、カーボンブ
ラック2部、50メツシーの真鋳粉 ′(末20部
、ニトリルゴム10部、重質炭酸カルシウム18部を加
え実施例1と同様に処理して銭金素地用フェノール樹脂
成形材料を得た。Example 2 To 40 parts of the same phenolic resin as in Example 1, 8 parts of hexamethylenetetramine, 2 parts of stearic acid, 2 parts of carbon black, 50 parts of brass powder (20 parts of powder, 10 parts of nitrile rubber, heavy 18 parts of calcium carbonate was added and treated in the same manner as in Example 1 to obtain a phenolic resin molding material for coin bases.
従来例
実施例1と同じフェノール樹脂40部 に対し、ヘキ
サメチレンテトラミン8部、ステアリン酸2部、カーボ
ンブラック2部、100メ・ソシュの木粉40部、重質
炭酸カルシウム8部を加え実施例1と同様に処理してフ
ェノール樹脂成形材料を得た〔発明の効果〕
実施例1及び2と従来例のフェノール樹脂成形材料を成
形温度170℃、成形圧力150驚で1分間成形して厚
み3簡の成形品を得、該成形品をトリクロルエチレンで
脱脂、10%水酸化ナトリウム溶液での予備エツチング
、硫酸−燐酸mmクロム酸カリ混合溶液でのエツチング
、5%塩酸での中和後、25分間電気銅鍍金を施した結
果は第1表で明白なように本発明の鍍金素地用フェノー
ル樹脂成形材料から得られた成形品には美麗、強固な銅
鍍金が施されたが、従来例によるものは鍍金することが
できなく本発明の優れていることを確認した。Conventional Example: To 40 parts of the same phenolic resin as in Example 1, 8 parts of hexamethylenetetramine, 2 parts of stearic acid, 2 parts of carbon black, 40 parts of 100 Me Soche wood powder, and 8 parts of heavy calcium carbonate were added. [Effect of the invention] The phenolic resin molding materials of Examples 1 and 2 and the conventional example were molded for 1 minute at a molding temperature of 170°C and a molding pressure of 150 mm to a thickness of 3. A simple molded article was obtained, the molded article was degreased with trichlorethylene, pre-etched with a 10% sodium hydroxide solution, etched with a mixed solution of sulfuric acid, phosphoric acid and potassium chromate, and neutralized with 5% hydrochloric acid. As is clear from Table 1, the results of electrolytic copper plating for minutes show that beautiful and strong copper plating was applied to the molded products obtained from the phenolic resin molding material for plating bases of the present invention, but compared to the conventional example. It was confirmed that the present invention was superior because it could not be plated.
第1表 特許出願人 松下電工株式会社 代理人弁理士 竹 元 敏 丸 (ばか2名)Table 1 patent applicant Matsushita Electric Works Co., Ltd. Representative Patent Attorney Toshimaru Takemoto (2 idiots)
Claims (1)
なるフェノール樹脂成形材料において、更に導電性材料
とゴムを添加し成形品の体積抵抗率が105Ωm以下に
なるようにしたことを特徴とする鍍金素地用フェノール
樹脂成形材料。(1) A phenolic resin molding material consisting of a phenolic resin, a curing agent, a filler, a mold release agent, etc. is further added with a conductive material and rubber so that the volume resistivity of the molded product is 105 Ωm or less. A phenolic resin molding material for plating substrates.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9821783A JPS59223746A (en) | 1983-06-01 | 1983-06-01 | Phenolic resin molding material for substrate to be plated |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP9821783A JPS59223746A (en) | 1983-06-01 | 1983-06-01 | Phenolic resin molding material for substrate to be plated |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS59223746A true JPS59223746A (en) | 1984-12-15 |
Family
ID=14213800
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP9821783A Pending JPS59223746A (en) | 1983-06-01 | 1983-06-01 | Phenolic resin molding material for substrate to be plated |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59223746A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0218490A (en) * | 1988-07-06 | 1990-01-22 | Tokai Rubber Ind Ltd | Electroconductive resin composition |
-
1983
- 1983-06-01 JP JP9821783A patent/JPS59223746A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0218490A (en) * | 1988-07-06 | 1990-01-22 | Tokai Rubber Ind Ltd | Electroconductive resin composition |
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