JPS5898427A - Preparation of molded article from ceramic fiber - Google Patents

Preparation of molded article from ceramic fiber

Info

Publication number
JPS5898427A
JPS5898427A JP56192741A JP19274181A JPS5898427A JP S5898427 A JPS5898427 A JP S5898427A JP 56192741 A JP56192741 A JP 56192741A JP 19274181 A JP19274181 A JP 19274181A JP S5898427 A JPS5898427 A JP S5898427A
Authority
JP
Japan
Prior art keywords
organic binder
ceramic fibers
molded article
ceramic
impregnated
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.)
Granted
Application number
JP56192741A
Other languages
Japanese (ja)
Other versions
JPH0336777B2 (en
Inventor
Susumu Miyawaki
進 宮脇
Kenji Arai
健司 新井
Seiichi Inoue
井上 清一
Haruo Kawashima
川島 治雄
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.)
Saint Gobain TM KK
Original Assignee
Toshiba Monofrax 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 Monofrax Co Ltd filed Critical Toshiba Monofrax Co Ltd
Priority to JP56192741A priority Critical patent/JPS5898427A/en
Publication of JPS5898427A publication Critical patent/JPS5898427A/en
Publication of JPH0336777B2 publication Critical patent/JPH0336777B2/ja
Granted legal-status Critical Current

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  • Compositions Of Oxide Ceramics (AREA)
  • Inorganic Fibers (AREA)

Abstract

PURPOSE:To obtain a molded article of ceramic fibers capable of reducing the shrinkage thereof in use, by impregnating the ceramic fibers with a small amount of an organic binder, heat-treating the impregnated ceramic fibers at a specific temperature to burn the organic binder and crystallize the ceramic fibers. CONSTITUTION:Ceramic fibers are impregnated with an organic binder, e.g. phenolic resin and compressed to give bulky ceramic fibers. The resultant bulky ceramic fibers are then packed in a mold, and high-temperature air at 200- 900 deg.C is passed through the fibers to burn the organic binder and give the aimed molded article of the partially or wholly crystallized ceramic fibers. The resultant molded article is they preferably impregnated with an aqueous solution a chromium salt, e.g. chromium acetate.

Description

【発明の詳細な説明】 本発明はセラよ、タフアイバー成形体の製造方法に関す
る。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a Tough Eye Bar molded article.

近年、省エネルギーの要請から各種工業窯炉においても
炉壁へのセラミ、タフアイパー成形体の採用が普及して
いる。
In recent years, due to the demand for energy conservation, the adoption of ceramic and tough eyeper molded bodies for the furnace walls has become widespread in various industrial furnaces.

セラさ、タフアイバーはアルミナとシリカが重量比でほ
ぼl:1の原料調合物を溶融し、この溶融物に圧縮ガス
を吹製媒体として吹きつけ繊維化して造られている。−
41!ラミ、タフアイバーは上記O吹製の際、著しい急
冷を受けてガラス状態に保持される。
Cerasa and Tough Eye Bar are made by melting a raw material mixture of alumina and silica in a weight ratio of approximately 1:1, and blowing compressed gas as a blowing medium onto this melt to form fibers. −
41! Laminate and tough eye bars are kept in a glass state due to rapid cooling during the O-blowing process.

ところで、従来、セラミックファイバー成形体は上記の
ように製造され喪セラミックファイバーに主に無機質結
合材を含浸させ、圧縮してバルク状とした後、乾燥加熱
して結合材を硬化させて製造している。
By the way, conventionally, ceramic fiber molded bodies are manufactured as described above by impregnating ceramic fibers with mainly an inorganic binder, compressing them into a bulk shape, and then drying and heating them to harden the binder. There is.

上述のように製造されたセラミ、タフアイバー成形体を
例えば炉壁に用いた場合、セラミ。
When the ceramic or tough eye bar molded body produced as described above is used for example on a furnace wall, it is a ceramic.

タフアイバー成形体の収縮が大きく炉壁の層状剥離、目
地開きや亀裂が発生する等の欠点がある。
There are drawbacks such as large shrinkage of the Tough Iver molded product, which may cause delamination of the furnace wall, opening of joints, and cracking.

このセラミックファイバー成形体の収縮の原因は、セラ
(、り7アイパーのガラス状態が約1000℃で結晶化
し、ムライトを生じて綾線が収縮するえめである。
The cause of the shrinkage of the ceramic fiber molded body is that the glassy state of Ceramic fiber crystallizes at about 1000° C., producing mullite and shrinking the twill lines.

そこで、セラミックファイバーを予めtooo℃で熱処
理し、1000℃以下の収縮を起ヒさせておけば、成形
体として炉壁等に使用しても、使用時の収縮率が減少す
ることが考えられ↓。
Therefore, if the ceramic fiber is heat-treated at too high a temperature in advance to induce shrinkage below 1000°C, it is thought that the shrinkage rate during use will be reduced even if it is used as a molded body for furnace walls, etc. ↓ .

しかし、セラミックファイバーは断熱材であって100
0℃の高温で熱処理すること社多大のエネルギーを消費
するうえ、熱処理した繊維はその強度が低下して堆扱い
が離しいため、現実には実施される例は極めて少ない。
However, ceramic fiber is a heat insulating material and has a
Heat treatment at a high temperature of 0° C. consumes a large amount of energy, and the strength of the heat-treated fibers decreases, making it difficult to handle them, so there are very few cases in which this method is actually practiced.

本発明は上記事情に鑑みてなされたものであり、セラミ
ックファイバーに少量の有機質結合剤を含浸させ、結晶
化温度よシ低^温度で熱処理して有機質結合剤を燃焼さ
せるととKよp1結晶化させて使用時の収縮率を低下し
得るセラミックファイバー成形体の製造方法を提供しよ
うとするものである。
The present invention was made in view of the above-mentioned circumstances, and it is said that the ceramic fiber is impregnated with a small amount of organic binder, and then heat treated at a temperature lower than the crystallization temperature to burn off the organic binder. The purpose of the present invention is to provide a method for producing a ceramic fiber molded article that can reduce the shrinkage rate during use.

すなわち、本願第1の発明は、有機質結合剤を含浸させ
て圧縮したーぐルク状1月、り7γ4パー11c200
〜900CO高温空気を接触させて前記有機質結合剤を
燃焼させ、前記バルク状セラミ、り7アイ/寺−の一部
一しくは全部を結晶化させることを特徴とするものであ
る。
That is, the first invention of the present application is a glue-like material impregnated with an organic binder and compressed.
The method is characterized in that the organic binder is brought into contact with ~900 CO high temperature air to burn the organic binder, thereby crystallizing part or all of the bulk ceramic.

また、本願j#!2の発明は、有機質結合剤を含浸させ
て圧縮したバルク状セラミ、タフアイパーファイバーの
一部もしくは全部を結晶化させ、更にり党ム塩水溶液を
含浸させること¥C%黴とする4のである。
Also, wish j#! The invention of item 2 is to crystallize a part or all of Tough Eye Perfiber, which is a bulk ceramic impregnated with an organic binder and compressed, and further impregnated with an aqueous solution of aluminum salt to form a mold. .

本発明における有機質結合剤としては、例えば7!ノー
ルレジン等が挙げられる。こうし九7、ノールレジy等
の有機質結合剤の含浸割合と圧縮体のかさ比重及び空気
が通過する圧縮体の厚さとの関係は次のように設定する
ことが望ましi、すなわち、フェノールレジンの含浸量
が5−1通過させる空気が200’C12気圧の場合、
圧縮体Oかさ比重は0.1以上、空気が通過する圧縮体
の厚さは50−以上であることが必要であ夛、この条件
にないと7エノールレジンの燃焼熱が通過する空気とと
もに排熱されて、竜う建ツク7アイパーを結晶化するこ
とができない、同様に1フエノールレジンの含浸量が1
0−の場合、圧縮体のかさ比重は0.1以上、空気が通
過する圧縮体の厚さは30−以上であることが必要であ
る。
Examples of the organic binder in the present invention include 7! Examples include norresin. It is desirable to set the relationship between the impregnation ratio of an organic binder such as Koshi97 and Knoll Resin, the bulk specific gravity of the compressed body, and the thickness of the compressed body through which air passes, i. If the impregnated amount of 5-1 is 200'C12 atm of air,
The bulk specific gravity of the compressed body O must be 0.1 or more, and the thickness of the compressed body through which the air passes must be 50 mm or more. If these conditions are not met, the combustion heat of the 7 enol resin will be exhausted together with the air passing through. When heated, it is impossible to crystallize the 7 eyelids, similarly when the impregnated amount of 1 phenol resin is 1
In the case of 0-, the bulk specific gravity of the compressed body must be 0.1 or more, and the thickness of the compressed body through which air passes must be 30- or more.

本発明において空気の温度を200〜900℃の範囲と
したOは、200℃未滴にすると有機質結合剤を燃焼さ
せることができず、セラミックファイバーが結晶化しな
いためであり、900℃を超えるとエネルギー消費が大
きくなるためである。
In the present invention, the reason for setting the air temperature in the range of 200 to 900°C is because if the temperature of the air is not dropped at 200°C, the organic binder cannot be burned and the ceramic fibers will not crystallize. This is because energy consumption increases.

本願第2の発明におけるクロム塩としては、例えば酢酸
クロム、炭酸クロム等が挙げられる。
Examples of the chromium salt in the second invention of the present application include chromium acetate and chromium carbonate.

かかるクロム塩を酸化クロムに転化させる手段としては
、含浸後乾燥加熱する方法あるいは使用時の炉内等で酸
化り冒ムに転化させる方法を採用し得る。こうしたクロ
ム塩から転化した酸化クロムは、セラミ、り7アイパー
の収縮のもう一つの原因である繊維間の接点で起きる焼
結部を防止できるため、セラミ、り7アイ・f−成形体
の収縮率をよシ低下すゐことができる。また、竜ラン、
クツアイバー成形体中の酸化クロム含有量は1〜B−の
範囲にあることが必要である。これは1チ未滴になると
使用時に繊維間の焼結を防止する効果が少なく、8sを
超えると酸化クロムがセラミックファイバー成形体から
分離しやすくなり使用上不都合なためである。
As a means for converting such chromium salt into chromium oxide, a method of drying and heating after impregnation, or a method of converting into chromium oxide in a furnace or the like during use can be adopted. Chromium oxide converted from these chromium salts can prevent sintering that occurs at the contact points between fibers, which is another cause of shrinkage in ceramic, 7-eye and f- molded bodies. It can significantly reduce the rate. Also, Ryuran,
It is necessary that the chromium oxide content in the fiber molded body is in the range of 1 to B-. This is because if less than 1 inch drops, there is little effect in preventing sintering between fibers during use, and if it exceeds 8 seconds, chromium oxide tends to separate from the ceramic fiber molded body, which is inconvenient in use.

本発明によれば、女うi、タフアイパーに少量の有機質
結合剤を含浸させ、結晶化温度よ)低い温度で熱処理し
て有機質結合剤を燃焼させることKよシ、断熱材である
セラミックファイバーを空気に結晶化できるので、エネ
ルギー消費は小さくてすみしかも#!維の強度の低下に
よる取扱いの困難も生じな−、i九、結晶化はバルク状
セラミ、タフアイパー圧縮体の中心から始まるので、通
過させる空気の温度あるいは通過時間の変化により結晶
化の範囲を;ントロールして成形体の外周付近は結晶化
させないようにすることもできる、このような外周付近
が結晶化していない成形体は外周付近で柔軟性が維持さ
れているため取扱いが容易で、炉壁に施工する場合、成
形体間を充分に密着させて目地開きを生じさせない、さ
らに得られた成形体は任意の形状に切断して種々の用途
に供し得る。
According to the present invention, by impregnating tough eyewear with a small amount of organic binder and heat-treating it at a low temperature (lower than the crystallization temperature) to burn out the organic binder, ceramic fiber, which is a heat insulating material, can be used. Since it can be crystallized in the air, energy consumption is small and #! Difficulties in handling may occur due to a decrease in the strength of the fibers.9.Since crystallization begins from the center of the bulk ceramic or Tough Eyeper compressed body, the range of crystallization can be controlled by changing the temperature or passing time of the air passing through it. It is also possible to prevent crystallization near the outer periphery of the molded object by controlling the outer periphery of the molded object. Such a molded object that is not crystallized near the outer periphery is easy to handle because flexibility is maintained near the outer periphery, and the furnace wall When carrying out construction, the molded bodies are brought into close contact sufficiently to prevent joint opening, and furthermore, the molded bodies obtained can be cut into any shape and used for various purposes.

以下、本発明の詳細な説明する。The present invention will be explained in detail below.

実施例1 常法により得られたセフ建、タフアイバーに78ノール
レジンをsl含浸させ、圧縮してバルク状セヲン、クフ
ァイバーを作製した。圧縮体のかさ比重は0.1、空気
が通過する圧縮体の厚さは50■であった。つづいて、
このバルク状セラミ、タフアイバーをモールド中に充填
し、200℃、2気圧の高温空気を繊維間に通過させた
。この際、数分間の空気の通過によるフェノールレジン
は硬化してブロック状の成形体が得られ、更に空気の通
過を続けると硬化し皮フ。
Example 1 A bulk fiber was impregnated with 78nol resin and compressed to produce a bulk fiber. The bulk specific gravity of the compressed body was 0.1, and the thickness of the compressed body through which air passed was 50 cm. Continuing,
This bulk ceramic and Tough Eye Bar were filled into a mold, and high-temperature air at 200° C. and 2 atm was passed between the fibers. At this time, the phenol resin hardens as air passes through it for several minutes to obtain a block-shaped molded product, and as air continues to pass through it, it hardens and becomes skin-like.

ノールレシンが燃焼して約1000℃とtkjI、一部
が結晶化したセラオ、クファイバー成形体ヲ得実施例2 実施例1で得られた、一部が結晶化し九セラiyクファ
イバー成形体に酢酸クロム水溶液を含浸させた。この後
、乾燥加熱して酢酸クロムt−酸化クロムに転化し、酸
化クロム含有量4−のセラミ、タフアイバー成形体を得
た。
Example 2 Norresin was combusted to a temperature of about 1000°C, and a partially crystallized CEL fiber molded body was obtained. Impregnated with chromium aqueous solution. Thereafter, the mixture was dried and heated to convert it into chromium acetate t-chromium oxide, thereby obtaining a ceramic and tough eye bar molded body having a chromium oxide content of 4-.

上記実施例2で最初に用いるセラミ、タフアイバー成形
体は一部が結晶化されているため表面が平滑でなく、酢
酸クロム水溶液を十分に含浸させることができ、乾燥、
加熱後に酢酸タロムから転化した酸化クロムはセラミ、
タフアイバーの表面に均一に分散される。
The ceramic/tough eye bar molded body used first in Example 2 has a partially crystallized surface, so the surface is not smooth and can be sufficiently impregnated with the chromium acetate aqueous solution.
Chromium oxide converted from tarom acetate after heating produces ceramic,
Evenly distributed on the surface of the tough eye bar.

上記実施例1及び実施例2で得られたセラミックファイ
バー成形体を種々の温度下に24時時間待し、その線収
縮率を測定して下記表に示した。なお、下記表には比較
のために従来方法で製造し良セツミ、クファイノ肴−成
形体の同一条件下での線収縮率を同時に示し次。
The ceramic fiber molded bodies obtained in Examples 1 and 2 were kept at various temperatures for 24 hours, and their linear shrinkage rates were measured and are shown in the table below. For comparison, the table below also shows the linear shrinkage percentages of molded products made using conventional methods under the same conditions.

表        単位 − 上記表から明らかなように実施例1で得られた一部結晶
化したセラミ、り7アイノ電−成形体は従来方法で得ら
れ九セラミック、ファイバー成形体より4M収縮率が低
下し、実施例2で得られた酸化り四ムを含有するセラミ
、タフアイバー成形体は実施例1のセラミ、タフアイバ
ー成形体より4更に線収縮率が低下した。
Table Unit - As is clear from the above table, the partially crystallized ceramic fiber molded body obtained in Example 1 had a 4M shrinkage rate lower than that of the nine ceramic fiber molded body obtained by the conventional method. The linear shrinkage rate of the ceramic/tough eye bar molded article containing oxide obtained in Example 2 was 4 times lower than that of the ceramic/tough eye bar molded article of Example 1.

以上詳述した如く本発明によれば、簡易な熱処理によシ
収縮率を低下させ、炉内で使用し九場合、炉壁の層状剥
離、目地開きや亀裂の発生を防止し得るセラミ、タフア
イバー成形体の製造方法ならびに酸化クロムを含有させ
ることにより更に収縮率を低下し得るセラミ、タフアイ
バー成形体の製造方法を提供できるものである。
As detailed above, according to the present invention, ceramics and tough eye bars can reduce the shrinkage rate through simple heat treatment, and can prevent delamination, joint opening, and cracking on the furnace wall when used in a furnace. It is possible to provide a method for producing a molded article and a method for producing a ceramic or tough eye bar molded article whose shrinkage rate can be further reduced by incorporating chromium oxide.

Claims (2)

【特許請求の範囲】[Claims] (1)  有機質結合剤を含浸させて圧縮したバルク状
セツにツクファイバーに200〜900℃の高温空気t
−接触させて前記有機質結合剤を燃焼させ、前記バルク
状セラミ、タフアイバーの一部もしくは全部を結晶化さ
せることを特徴とするセラミックファイバー成形体の製
造方法。
(1) High-temperature air at 200 to 900°C is applied to bulk fibers impregnated with an organic binder and compressed.
- A method for producing a ceramic fiber molded article, which comprises bringing the organic binder into contact with the material to burn it, and crystallizing part or all of the bulk ceramic or tough eye bar.
(2)有機質結合剤を含浸させて圧縮したバルク状セラ
ミ、タフアイバーに200〜900℃の高温空気を接触
させて前記有機質結合剤を燃焼させ、前記バルク状セラ
書ツクファイバーの一部もシ〈は全部を結晶化させ、更
にクロム塩水溶液を含浸させることを特徴とするセフ?
yり7アイパ一成形体の製造方法。
(2) Bulk ceramic or tough fiber impregnated with an organic binder and compressed is brought into contact with high-temperature air at a temperature of 200 to 900°C to burn the organic binder, and a portion of the bulk ceramic fiber is also burned. Cef? is characterized by crystallizing the entire product and further impregnating it with an aqueous chromium salt solution.
A method for producing a molded article.
JP56192741A 1981-12-02 1981-12-02 Preparation of molded article from ceramic fiber Granted JPS5898427A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56192741A JPS5898427A (en) 1981-12-02 1981-12-02 Preparation of molded article from ceramic fiber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56192741A JPS5898427A (en) 1981-12-02 1981-12-02 Preparation of molded article from ceramic fiber

Publications (2)

Publication Number Publication Date
JPS5898427A true JPS5898427A (en) 1983-06-11
JPH0336777B2 JPH0336777B2 (en) 1991-06-03

Family

ID=16296282

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56192741A Granted JPS5898427A (en) 1981-12-02 1981-12-02 Preparation of molded article from ceramic fiber

Country Status (1)

Country Link
JP (1) JPS5898427A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20180096807A (en) * 2016-01-19 2018-08-29 유니프랙스 아이 엘엘씨 Inorganic fiber

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55154380A (en) * 1979-05-21 1980-12-01 Carborundum Co Chromium oxide clad refractory fiber
JPS5830272A (en) * 1981-08-18 1983-02-22 Fuji Xerox Co Ltd Fixed platen type original multicolor reader

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55154380A (en) * 1979-05-21 1980-12-01 Carborundum Co Chromium oxide clad refractory fiber
JPS5830272A (en) * 1981-08-18 1983-02-22 Fuji Xerox Co Ltd Fixed platen type original multicolor reader

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20180096807A (en) * 2016-01-19 2018-08-29 유니프랙스 아이 엘엘씨 Inorganic fiber
CN108779020A (en) * 2016-01-19 2018-11-09 尤尼弗瑞克斯 I 有限责任公司 Inorfil
JP2019503332A (en) * 2016-01-19 2019-02-07 ユニフラックス ワン リミテッド ライアビリティ カンパニー Inorganic fiber

Also Published As

Publication number Publication date
JPH0336777B2 (en) 1991-06-03

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