JPH01287265A - Carbonaceous composite material - Google Patents

Carbonaceous composite material

Info

Publication number
JPH01287265A
JPH01287265A JP11363388A JP11363388A JPH01287265A JP H01287265 A JPH01287265 A JP H01287265A JP 11363388 A JP11363388 A JP 11363388A JP 11363388 A JP11363388 A JP 11363388A JP H01287265 A JPH01287265 A JP H01287265A
Authority
JP
Japan
Prior art keywords
resin
substrate
skeletal structure
noble metal
vitreous
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
JP11363388A
Other languages
Japanese (ja)
Inventor
Hideyasu Matsuo
松尾 秀逸
Kazuo Ito
和男 伊藤
Koichi Imura
浩一 井村
Masatoshi Kasahara
笠原 雅寿
Masaaki Kanamori
正晃 金森
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.)
Coorstek KK
Original Assignee
Toshiba Ceramics 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 Toshiba Ceramics Co Ltd filed Critical Toshiba Ceramics Co Ltd
Priority to JP11363388A priority Critical patent/JPH01287265A/en
Publication of JPH01287265A publication Critical patent/JPH01287265A/en
Pending legal-status Critical Current

Links

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  • Physical Vapour Deposition (AREA)
  • Chemical Vapour Deposition (AREA)
  • Other Surface Treatments For Metallic Materials (AREA)

Abstract

PURPOSE:To develop the title high-strength carbonaceous material appropriate for catalyst, etc., by forming a substrate of three-dimensional skeletal structure with the vitreous carbon fulfilling specified requirements, and forming a noble metal film on the surface. CONSTITUTION:Soft polyester-based polyurethane foam of three-dimensional skeletal structure is uniformly impregnated with a resin such as furfuryl alcohol polymer. The material is then heated at 150 deg.C to dry and cure the resin, and then calcined at 950 deg.C in a non-oxidizing atmosphere to carbonize the polyurethane foam. The resin is converted to vitreous carbon, and the vitreous-carbon substrate of three-dimensional skeletal structure having open cells in the skeleton is formed. The size La (Angstrom ) of the crystallite of the vitreous carbon is controlled to <=300Angstrom , and the sp. gr. by the butanol dip method of the substrate is adjusted to <=1.70g/cc. A thin film of a noble metal such as Pt, Pd, Au, and Ag is formed thereon by sputtering to produce a high-strength carbonaceous composite material capable of being used for catalyst.

Description

【発明の詳細な説明】 L組L列札脂飢1 この発明はノコ−ボン質複合月y4に関する。[Detailed description of the invention] L group L row bill fat starvation 1 This invention relates to the nocobonic composite moon y4.

従来の技術 三次元骨格構造を有する金属多孔体の触媒は従来公知で
ある。たとえば、発泡ウレタンフオームの表面にNi等
の電気メツキを施し=  1  − たあど、ウレタンフオームを焼去ざせることにより連通
孔を有する発泡金属にして触媒を構成している。
BACKGROUND OF THE INVENTION Porous metal catalysts having a three-dimensional skeleton structure are known in the art. For example, the surface of a foamed urethane foam is electroplated with Ni or the like, and then the urethane foam is burned off to form a foamed metal having communicating holes to form a catalyst.

一明が解′(シようとL乞l」劇 従来の発泡金属においては、三次元骨格の断面がウレタ
ンフオームの焼去後に空洞とIノで残存づる。
In conventional metal foam, the cross section of the three-dimensional skeleton remains in the form of cavities and holes after the urethane foam is burned out.

発泡金属のみで成りたっているため、骨格構造の強度が
小ざくなる欠点があった。
Since it was made only of foamed metal, it had the disadvantage that the strength of the skeletal structure was reduced.

発明の目的 そこで、この発明(J、従来の三次元骨格の金属多孔体
に比較し−(強度を向上さぜるこどのてきるカーボン′
fI複合材利、例えば触媒等に用いる複合1t3 J”
lを提供することを目的としている。
Purpose of the Invention Therefore, the present invention (J) is based on carbon'
fI composite materials, such as composite 1t3J used for catalysts, etc.
The aim is to provide l.

几Jし生方」L 前jホの1的を達成づるために、この発明は請求項1に
記載したカーボン質複合月利を要一  2  一 旨としている。
In order to achieve the first objective of the above, the present invention focuses on the carbonaceous composite monthly interest rate set forth in claim 1.

ロ −「を ′するための二゛ 所定の条件をみたずガラス状ノJ−ボンににつで三次元
骨格構造の基材を構成し、その基材の表面に薄膜状にP
t 、 Pd 、△1」またはA(+の貴金属を被覆し
た。
In order to achieve this, a base material with a three-dimensional skeleton structure is constructed of glass-like J-bonds, and a thin film of P is applied to the surface of the base material, without meeting certain conditions.
t, Pd, △1'' or A(+ noble metal was coated.

11丸」 基材がガラス状カーボンよりなり高強度を有するため、
複合1の強度を大ぎくできる。
11 Maru” Because the base material is made of glassy carbon and has high strength,
The strength of Composite 1 can be greatly increased.

また、貴金属の薄膜の厚みを小さくしても、強度上の問
題が生じない。
Further, even if the thickness of the noble metal thin film is made small, no strength problems arise.

尖皿に 三次元骨格構造のポーラスな軟質のポリニスデル系ウレ
タンフオームに樹脂(たとえばフルフリルアルコール重
合物)を付着さぜる。
A resin (for example, furfuryl alcohol polymer) is attached to a porous soft polynisder urethane foam with a three-dimensional skeleton structure on a pointed plate.

たどえば、ウレタンフオームにフリフリルアルコール手
合物を含浸させる操作において、目詰まりがなく、かつ
均一に脱液が行えるJニうに遠心脱液装置を用いて含浸
するのが好ましい。
For example, in the operation of impregnating the urethane foam with the frifuryl alcohol compound, it is preferable to impregnate the urethane foam using a centrifugal dewatering device that does not cause clogging and can uniformly remove the fluid.

そのあと、150’Cで樹脂を乾燥硬化させる。しかる
後、非酸化性雰囲気(たとえば窒素雰囲気)において9
50℃で焼成覆る。この焼成によりウレタンフオームは
炭化し、樹脂はガラス状カーボンとなり、骨格中に連通
孔を右するガラス状カーボン三次元骨格構造基材を形成
づる。
Thereafter, the resin is dried and cured at 150'C. Thereafter, in a non-oxidizing atmosphere (e.g. nitrogen atmosphere) 9
Cover and bake at 50°C. By this firing, the urethane foam is carbonized, the resin becomes glassy carbon, and a three-dimensional glassy carbon skeleton structure base material having communicating holes in the skeleton is formed.

なお、前述の含浸→硬化→焼成の工程を複数回くり返し
たり、焼成後に純化のために塩素ガスと接触させながら
約2300 ’Cで加熱してもにい。
In addition, the above-mentioned impregnation → hardening → firing process may be repeated several times, or after firing, the material may be heated at about 2300'C while being brought into contact with chlorine gas for purification.

ガラス状カーボンの結晶子の大ぎさ1a(X)が300
人よりも大きいと、結晶子が大ぎずぎるため、強度の低
下がみられる。また、ブタノール浸漬法の比重が1.7
0q/CCよりも大ぎいど、製造が極めて困難となる。
The crystallite size 1a (X) of glassy carbon is 300
If it is larger than a human, the crystallites will be too large, resulting in a decrease in strength. In addition, the specific gravity of the butanol immersion method is 1.7.
If it is larger than 0q/CC, manufacturing becomes extremely difficult.

前述のようにして作られた三次元骨格構造のガラス状カ
ーボン基材の表面にスパッタリング法ににすPt 、P
d 、AUまたはAgの薄膜を形成1ノ、各骨格の表面
を被覆する。、薄膜の厚みは20μn1未満であると二
次元骨格構造の強度が十分でなく、2mmを越えると三
次元骨格構造の空隙が少なくなるので、20μm〜2m
mが好ましい。スパッタリング法以外の方法(たとえば
、プラズマ法、電解メツキ法、非電解メツキ法、CVD
法等)によって薄膜を形成してもJ:い。
Pt and P were sputtered onto the surface of the glassy carbon substrate with the three-dimensional skeleton structure prepared as described above.
d. Form a thin film of AU or Ag to coat the surface of each skeleton. If the thickness of the thin film is less than 20 μm, the strength of the two-dimensional skeleton structure will not be sufficient, and if it exceeds 2 mm, the voids in the three-dimensional skeleton structure will decrease.
m is preferred. Methods other than sputtering (for example, plasma method, electrolytic plating method, non-electrolytic plating method, CVD method)
J: It is not possible to form a thin film by a method such as a method.

Claims (1)

【特許請求の範囲】[Claims] 1、結晶子の大きさLa(Å)が300Å以下で、ブタ
ノール浸漬法の比重が1.70g/cc以下であるガラ
ス状カーボンからなるカーボン三次元骨格構造基材の表
面にPt、Pd、AuまたはAgの貴金属の薄膜を被覆
したことを特徴とするカーボン質複合材料。
1. Pt, Pd, Au on the surface of a three-dimensional carbon skeleton structure base material made of glassy carbon whose crystallite size La (Å) is 300 Å or less and the specific gravity by butanol immersion method is 1.70 g/cc or less Or, a carbonaceous composite material characterized by being coated with a thin film of a noble metal such as Ag.
JP11363388A 1988-05-12 1988-05-12 Carbonaceous composite material Pending JPH01287265A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11363388A JPH01287265A (en) 1988-05-12 1988-05-12 Carbonaceous composite material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11363388A JPH01287265A (en) 1988-05-12 1988-05-12 Carbonaceous composite material

Publications (1)

Publication Number Publication Date
JPH01287265A true JPH01287265A (en) 1989-11-17

Family

ID=14617181

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11363388A Pending JPH01287265A (en) 1988-05-12 1988-05-12 Carbonaceous composite material

Country Status (1)

Country Link
JP (1) JPH01287265A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003516508A (en) * 1999-12-07 2003-05-13 エスケイエフ エンジニアリング アンド リサーチ センター ビーブイ Drum brakes and electric actuators therefor

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5161404A (en) * 1974-11-27 1976-05-28 Ulvac Corp Kinzokuzairyoto tansosenitokaranaru fukugozairyono seizoho
JPS5579871A (en) * 1978-12-06 1980-06-16 Sumitomo Electric Ind Ltd Metal covering method for non-conductive substance

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5161404A (en) * 1974-11-27 1976-05-28 Ulvac Corp Kinzokuzairyoto tansosenitokaranaru fukugozairyono seizoho
JPS5579871A (en) * 1978-12-06 1980-06-16 Sumitomo Electric Ind Ltd Metal covering method for non-conductive substance

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003516508A (en) * 1999-12-07 2003-05-13 エスケイエフ エンジニアリング アンド リサーチ センター ビーブイ Drum brakes and electric actuators therefor

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