JPH0240636B2 - TANSOKABUTSUHENOKINZOKUHIFUKUHOHO - Google Patents

TANSOKABUTSUHENOKINZOKUHIFUKUHOHO

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Publication number
JPH0240636B2
JPH0240636B2 JP23891883A JP23891883A JPH0240636B2 JP H0240636 B2 JPH0240636 B2 JP H0240636B2 JP 23891883 A JP23891883 A JP 23891883A JP 23891883 A JP23891883 A JP 23891883A JP H0240636 B2 JPH0240636 B2 JP H0240636B2
Authority
JP
Japan
Prior art keywords
metal
molded body
chlorine
containing resin
metal coating
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.)
Expired - Lifetime
Application number
JP23891883A
Other languages
Japanese (ja)
Other versions
JPS60192698A (en
Inventor
Takao Koyama
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 Pencil Co Ltd
Original Assignee
Mitsubishi Pencil 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 Pencil Co Ltd filed Critical Mitsubishi Pencil Co Ltd
Priority to JP23891883A priority Critical patent/JPH0240636B2/en
Publication of JPS60192698A publication Critical patent/JPS60192698A/en
Publication of JPH0240636B2 publication Critical patent/JPH0240636B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Description

【発明の詳細な説明】 〔発明の詳細な説明〕 本発明は炭素化物への金属被覆方法に関する。[Detailed description of the invention] [Detailed description of the invention] The present invention relates to a method for metal coating carbonized materials.

従来、炭素化物への金属被覆にはイオンスパツ
タ法、プラズマ法、電解メツキ法、化学メツキ法
などがあつた。しかし、これらの方法には、 (1) 大きな物や複雑な形状の物への金属被覆が困
難である、 (2) 複雑な形状の物に対して細部までの被覆を行
うことが困難である、 (3) 装置が高価であり、操作が複雑であるなどの
欠点があつた。
Conventionally, methods such as ion sputtering method, plasma method, electrolytic plating method, and chemical plating method have been used to coat carbonized materials with metal. However, these methods have the following drawbacks: (1) It is difficult to coat metal on large objects or objects with complex shapes; (2) It is difficult to coat fine details on objects with complex shapes. (3) There were disadvantages such as the equipment was expensive and the operation was complicated.

本発明の目的は、これらの欠点のない比較的簡
単な工程によつて充分な被覆を行うことのできる
炭素化物への金属被覆方法を提供することであ
る。
An object of the present invention is to provide a method for metal coating carbonized materials, which does not have these disadvantages and can provide sufficient coating through relatively simple steps.

本発明者は鋭意研究の結果、金属と接触させた
含塩素系樹脂を電気炉を用いて不活性雰囲気中で
所定の温度まで加熱焼温し、一部又は全部が含塩
素樹脂である該配合物を炭素化させる過程で、炭
素化物への金属接触面をCrまたはFe−Crで被覆
することを特徴とする本発明によつてこの目的を
達成するを得た。
As a result of intensive research, the present inventor has determined that a chlorine-containing resin that has been brought into contact with a metal is heated to a predetermined temperature in an inert atmosphere using an electric furnace, and that This object has been achieved by the present invention, which is characterized in that the metal contact surface to the carbonized material is coated with Cr or Fe-Cr during the process of carbonizing the material.

本発明においては、一部又は全部が含塩素系の
である配合物に金属CrまたはFe−Cr系合金の粉
末状、枝状、棒状、糸状のものを直接接触させ
る。このため該配合物の形状に合わせて種々な形
のものに金属を被覆させることができる。
In the present invention, a powdered, branched, rod-shaped, or thread-shaped Cr metal or Fe-Cr alloy is brought into direct contact with a mixture that is partially or entirely chlorine-containing. Therefore, various shapes can be coated with metal depending on the shape of the compound.

ここで本発明の炭素化物への金属被覆方法で用
いる含塩素系樹脂はポリ塩化ビニル(PVC)、ポ
リ塩化ビニリデン、塩化ゴムなどの組成に塩素を
含む樹脂のことである。
The chlorine-containing resin used in the method of metal coating a carbonized material of the present invention is a resin containing chlorine in its composition, such as polyvinyl chloride (PVC), polyvinylidene chloride, or chlorinated rubber.

本発明に使用する金属は、金属Cr、Cr−Fe系
合金などCrを含む金属であり、その形状は、板
状、棒状、糸状、粉状などである。
The metal used in the present invention is a metal containing Cr, such as Cr metal or a Cr-Fe alloy, and its shape is plate-like, rod-like, thread-like, powder-like, etc.

次に、該配合物は含塩素系樹脂とこれ(1)を相溶
する有機高分子化合物又はその初期縮合体との混
合物であり、含塩素系樹脂は少なくとも20Wt%
含有するものである。または含塩素系樹脂と黒鉛
セラミツクスなどの無機フイラーとの混合物であ
り、含塩素系樹脂は少なくとも20Wt%含有する
ものである。これらの配合物と金属とを接触させ
たまま電気炉中で不活性ガス雰囲気下において、
1100℃で焼結を行う。
Next, the compound is a mixture of a chlorine-containing resin and an organic polymer compound or an initial condensate thereof that is compatible with (1), and the chlorine-containing resin is at least 20% by weight.
It contains. Alternatively, it is a mixture of a chlorine-containing resin and an inorganic filler such as graphite ceramics, and the chlorine-containing resin contains at least 20% by weight. These compounds are kept in contact with the metal in an electric furnace under an inert gas atmosphere,
Sintering is performed at 1100℃.

焼成温度、焼成スピード、焼成時間等は配合物
を構成している物質によつて異なる。
Firing temperature, firing speed, firing time, etc. vary depending on the substances constituting the compound.

かかる本発明の炭素化物への金属被覆方法によ
れば金属との接触さへ可能ならば任意の炭素製品
の形状に合わせて金属被覆ができる、しかも使用
した金属はヤスリなどを用いて新しい金属面を出
すことにより金属自体が消耗するまで繰返して使
用できる。このように本発明の方法は複雑は操
作、手間を必要とせず、高価な装置も必要としな
い。さらに使用する電気炉の容積内で種々の大き
さ又は形状の炭素製品への金属被覆ができるとと
もに使用した金属は消耗するまで繰返し使用可能
でありコストの低減をはかる上でも有利な方法で
ある。
According to the method of metal coating a carbonized product of the present invention, metal coating can be applied to suit the shape of any carbon product if possible, and the used metal can be polished to a new metal surface using a file or the like. By releasing the metal, it can be used repeatedly until the metal itself is exhausted. Thus, the method of the present invention does not require complicated operations, labor, or expensive equipment. Furthermore, carbon products of various sizes or shapes can be coated with metal within the volume of the electric furnace used, and the used metal can be used repeatedly until it is exhausted, making it an advantageous method for reducing costs.

次に本発明を実施例について説明する。なお、
本発明はかかる実施例によつて限定されるもので
はなく本発明の技術的思想の及ぶ範囲において自
由に変更できるものである。
Next, the present invention will be explained with reference to examples. In addition,
The present invention is not limited to these examples, but can be freely modified within the scope of the technical idea of the present invention.

実施例 1 塩素化塩化ビニル100g、10μm程度の粒度を
もつ黒鉛粉体400g及びジアリルフタレートモノ
マー300gをヘンシエルミキサーで10分間混合し、
得られた混合物を2本ロールを用いて混練し、次
いでフイルム状に成形した。このフイルムをプラ
ンジヤーにより2mmφの丸棒状に押し出し、100
mmに切断して得られた丸棒状成形物を、第1図に
示すごとく、粒径100μm以下の粒末状SUS−302
ステンレススチールで覆うようにセツトし、次い
で第3図に示す横型電気炉を用いて不活性雰囲気
中5℃/hrで300℃まで昇温させ、さらに20℃/
hrで1100℃まで昇温させ1100℃で3時間保持し、
その後然冷却を行つた。得られた炭化物の金属接
触面は銀灰色であつた。X線マイクロアナライザ
ー、(以下XMAと称する)によつて得られた結
果を第4図に示す。
Example 1 100 g of chlorinated vinyl chloride, 400 g of graphite powder with a particle size of about 10 μm, and 300 g of diallyl phthalate monomer were mixed for 10 minutes in a Henschel mixer.
The resulting mixture was kneaded using two rolls and then formed into a film. This film was extruded into a round bar shape of 2 mmφ with a plunger, and
As shown in Fig. 1, the round rod-shaped molded product obtained by cutting into mm pieces is made of granular SUS-302 with a particle size of 100 μm or less.
It was set so as to be covered with stainless steel, and then heated to 300°C at a rate of 5°C/hr in an inert atmosphere using a horizontal electric furnace shown in Figure 3, and further heated to 20°C/hr.
Raise the temperature to 1100℃ with hr and hold at 1100℃ for 3 hours,
Cooling was then performed. The metal contact surface of the obtained carbide was silvery gray. Figure 4 shows the results obtained using an X-ray microanalyzer (hereinafter referred to as XMA).

得られた銀灰色物の成分はCrと中心としFeを
少々含むものであることが確認できた。しかも銀
灰色物は炭素材表面均一に被覆されていた。
It was confirmed that the components of the obtained silvery gray material were mainly Cr and contained a small amount of Fe. Furthermore, the silvery gray material was uniformly coated on the surface of the carbon material.

実施例 2 塩素化塩化ビニル400g、フラン樹脂200g、粒
径が10μm以下の黒鉛粉末400g、ジアリルフタ
レートモノマー200gをステンレススチールの容
器に投入し、混合を行い、得られた混合物を2本
ロールを用いて混練し、次いでフイルム状に成形
した。得られたフイルムは厚さ500μm程度で、
これを平らに引延し50mmx50mmの正方形に形成し
た。
Example 2 400 g of chlorinated vinyl chloride, 200 g of furan resin, 400 g of graphite powder with a particle size of 10 μm or less, and 200 g of diallyl phthalate monomer were placed in a stainless steel container, mixed, and the resulting mixture was transferred using two rolls. The mixture was kneaded and then formed into a film. The obtained film has a thickness of about 500 μm,
This was drawn flat and formed into a 50 mm x 50 mm square.

これを第2図に示すごとく100mmx100mmx2mmの
板状SUS−302ステンレススチールではさみこむ
ようにしてセツトし、次いで第3図の横型電気炉
を用いて窒素ガス雰囲気中で5℃/hrで300℃ま
で昇温させ、さらに、20℃/hrで1100℃まで昇温
させた後1100℃で3時間保持し、その後自然冷却
を行つた。得られた炭化物の金属接触面は銀灰色
をしており、XMAによつて銀灰色物の成分を調
べた結果CrとFeであることが確認できた。
As shown in Figure 2, this was sandwiched between 100 mm x 100 mm x 2 mm plates of SUS-302 stainless steel, and then heated to 300 °C at a rate of 5 °C/hr in a nitrogen gas atmosphere using the horizontal electric furnace shown in Figure 3. The temperature was then raised to 1100°C at a rate of 20°C/hr, held at 1100°C for 3 hours, and then allowed to cool naturally. The metal contact surface of the obtained carbide had a silvery gray color, and as a result of examining the components of the silvery gray substance by XMA, it was confirmed that it was Cr and Fe.

実施例 3 (全部が含塩素化塩化ビニル樹脂のみの場合) 塩素化塩化ビニル樹脂粉末400gとジアリルフ
タレートモノマー200gをヘンシエルミキサーで
良く混合し、得られた混合物を2本ロールを用い
て混練し、次いでフイルム状に成形した。
Example 3 (In the case where all of the resin is chlorinated vinyl chloride resin) 400 g of chlorinated vinyl chloride resin powder and 200 g of diallyl phthalate monomer were thoroughly mixed in a Henschel mixer, and the resulting mixture was kneaded using two rolls. Then, it was formed into a film.

得られたフイルムを、第2図に示したように、
金属Cr板ではさみこむようにセツトし、次いで、
第3図に示す横型電気炉を用いて、窒素ガス雰囲
気中で、5℃/時間で300℃まで昇温させ、さら
に20℃/時間で1100℃まで昇温させた後、1100℃
で3時間保持し、その後、自然冷却を行つた。得
られた炭化物シートの金属Cr接触面は銀灰色を
呈しており、XMAにより銀灰色の成分がCrであ
ることが確認された。
As shown in Fig. 2, the obtained film was
Set it so that it is sandwiched between metal Cr plates, and then
Using the horizontal electric furnace shown in Figure 3, the temperature was raised to 300°C at a rate of 5°C/hour in a nitrogen gas atmosphere, then further raised to 1100°C at a rate of 20°C/hour, and then heated to 1100°C.
The mixture was held for 3 hours and then naturally cooled. The metal-Cr contact surface of the obtained carbide sheet had a silver-gray color, and it was confirmed by XMA that the component of the silver-gray color was Cr.

実施例 4 (黒鉛粉末以外の無機粉末を使用した場合) 塩素化塩化ビニル樹脂粉末600g、平均粒子直
径で5μm程度の粒子直径を持つB4C粉末200g及
びジアリルフタレートモノマー300gをヘンシエ
ルミキサーで充分に混合し、得られた混合物を2
本ロールを用いて混練し、次いでフイルム状に成
形した。
Example 4 (When inorganic powder other than graphite powder is used) 600 g of chlorinated vinyl chloride resin powder, 200 g of B 4 C powder with an average particle diameter of about 5 μm, and 300 g of diallyl phthalate monomer were mixed in a Henschel mixer. and mix the resulting mixture with 2
The mixture was kneaded using this roll and then formed into a film.

このフイルムを、プランジヤーにより、1mmφ
の丸棒状に押し出し、100mmに切断して得られた
丸棒成形物を、第1図に示すように、平均粒子径
で100μm程度の粒子径を持つ粉末状金属Crで覆
うようにセツトし、次いで、第3図に示す横型電
気炉を用いて、窒素ガス雰囲気中で、5℃/時間
で300℃まで昇温させ、さらに、20℃/時間で
1100℃まで昇温させた後、1100℃で3時間保持
し、その後、自然冷却を行つた。得られた炭化物
シートの金属Cr接触面は銀灰色を呈しており、
XMAにより銀灰色の成分がCrであることが確認
された。
This film is 1mmφ with a plunger.
The round bar molded product obtained by extruding it into a round bar shape and cutting it into 100 mm pieces was set so as to be covered with powdered metal Cr having an average particle size of about 100 μm, as shown in Figure 1. Next, using the horizontal electric furnace shown in Fig. 3, the temperature was raised to 300°C at a rate of 5°C/hour in a nitrogen gas atmosphere, and further at 20°C/hour.
After raising the temperature to 1100°C, it was held at 1100°C for 3 hours, and then naturally cooled. The metal Cr contact surface of the obtained carbide sheet had a silvery gray color.
XMA confirmed that the silvery gray component was Cr.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は実施例1における丸棒状成形物をステ
ンレススチール粉で覆うてステンレススチールの
箱にセツトした状態を示す。図において、 1:ステンレススチールの箱、2:SUS−302
のステンレススチール粉末、3:丸棒状成形物、 第2図は実施例2におけるフイルム状成形物を
ステンレススチールの板にセツトした状態を示
す。図において、 4:SUS−302ステンレススチールの板、5:
フイルム状成形物、 第3図は金属被覆及び炭化焼成のための装置の
概略説明図である。図において、 6:試料、7:横型管状炉、8:黒鉛製保温
材、9:4N−NaOH水溶液、 第4図は図面に代わる写真で、aは実施例1の
丸棒の断面、bはCrの分布状態、cはFeの分布
状態のX線マイクロアナライザーによる写真であ
る。d:bがCrであることの確認図、e:cが
Feであることの確認図。
FIG. 1 shows the round rod-shaped molded product of Example 1 covered with stainless steel powder and set in a stainless steel box. In the figure, 1: Stainless steel box, 2: SUS-302
Stainless steel powder, 3: Round rod-shaped molded product, FIG. 2 shows the film-shaped molded product in Example 2 set on a stainless steel plate. In the figure, 4: SUS-302 stainless steel plate, 5:
FIG. 3 is a schematic diagram of an apparatus for metal coating and carbonization firing. In the figure, 6: Sample, 7: Horizontal tubular furnace, 8: Graphite heat insulating material, 9: 4N-NaOH aqueous solution, Figure 4 is a photograph in place of a drawing, a is a cross section of the round bar of Example 1, and b is Cr distribution state, c is a photograph taken by an X-ray microanalyzer of Fe distribution state. d: Confirmation diagram that b is Cr, e: c is
Diagram confirming that it is Fe.

Claims (1)

【特許請求の範囲】 1 一部、又は全部が含塩素樹脂である配合物を
適当な形に成形加工し、得られた成形体に金属
Cr、又はCr−Feを含有する金属に接触させ、不
活性雰囲気中で加熱昇温して該成形体を炭素化さ
せる過程において、該成形体の金属接触面をCr、
又はCr−Feで数μm程度に被覆することを特徴
とする炭素化物への金属被覆方法。 2 該成形体は、含塩素樹脂少なくとも20重量%
含む特許請求の範囲第1項に記載の炭素化物への
金属被覆方法。 3 該成形体は、含塩素樹脂とこれと相溶する有
機高分子化合物、又はその初期縮合体との混合物
から成る特許請求の範囲第1項に記載の炭素化物
の金属被覆方法。 4 該成形体は、含塩素樹脂と黒鉛、セラミツク
ス等の無機フイラーとの混合物から成る特許請求
の範囲第1項に記載の炭素化物への金属被覆方
法。 5 該炭素化における加熱温度は、被覆させる金
属の融点までの温度である特許請求の範囲第1項
に記載の炭素化物への金属被覆方法。
[Claims] 1. Molding a compound partially or entirely made of chlorine-containing resin into an appropriate shape, and molding the resulting molded body with metal.
In the process of bringing the molded body into contact with a metal containing Cr or Cr-Fe and carbonizing the molded body by heating and raising the temperature in an inert atmosphere, the metal contact surface of the molded body is exposed to Cr,
Alternatively, a method of metal coating a carbonide, characterized by coating with Cr-Fe to a thickness of about several μm. 2. The molded article contains at least 20% by weight of chlorine-containing resin.
A method for metal coating a carbonized material according to claim 1. 3. The method of metal coating a carbonized material according to claim 1, wherein the molded body is a mixture of a chlorine-containing resin and an organic polymer compound compatible therewith, or an initial condensate thereof. 4. The method for metal coating a carbonized product according to claim 1, wherein the molded body is a mixture of a chlorine-containing resin and an inorganic filler such as graphite or ceramics. 5. The method of metal coating a carbonized material according to claim 1, wherein the heating temperature in the carbonization is a temperature up to the melting point of the metal to be coated.
JP23891883A 1983-12-20 1983-12-20 TANSOKABUTSUHENOKINZOKUHIFUKUHOHO Expired - Lifetime JPH0240636B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP23891883A JPH0240636B2 (en) 1983-12-20 1983-12-20 TANSOKABUTSUHENOKINZOKUHIFUKUHOHO

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP23891883A JPH0240636B2 (en) 1983-12-20 1983-12-20 TANSOKABUTSUHENOKINZOKUHIFUKUHOHO

Publications (2)

Publication Number Publication Date
JPS60192698A JPS60192698A (en) 1985-10-01
JPH0240636B2 true JPH0240636B2 (en) 1990-09-12

Family

ID=17037205

Family Applications (1)

Application Number Title Priority Date Filing Date
JP23891883A Expired - Lifetime JPH0240636B2 (en) 1983-12-20 1983-12-20 TANSOKABUTSUHENOKINZOKUHIFUKUHOHO

Country Status (1)

Country Link
JP (1) JPH0240636B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5415061B2 (en) 2008-12-08 2014-02-12 東洋炭素株式会社 Carbon material manufacturing method and carbon material

Also Published As

Publication number Publication date
JPS60192698A (en) 1985-10-01

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