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JPH0148225B2 - - Google Patents

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Publication number
JPH0148225B2
JPH0148225B2 JP59085749A JP8574984A JPH0148225B2 JP H0148225 B2 JPH0148225 B2 JP H0148225B2 JP 59085749 A JP59085749 A JP 59085749A JP 8574984 A JP8574984 A JP 8574984A JP H0148225 B2 JPH0148225 B2 JP H0148225B2
Authority
JP
Japan
Prior art keywords
fibers
sio
firing
sol
fiber
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
Application number
JP59085749A
Other languages
Japanese (ja)
Other versions
JPS60231453A (en
Inventor
Fumihiko Hagiwara
Masaaki Yamamoto
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.)
Isolite Babcock Refractories Co Ltd
Original Assignee
Isolite Babcock Refractories 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 Isolite Babcock Refractories Co Ltd filed Critical Isolite Babcock Refractories Co Ltd
Priority to JP8574984A priority Critical patent/JPS60231453A/en
Publication of JPS60231453A publication Critical patent/JPS60231453A/en
Publication of JPH0148225B2 publication Critical patent/JPH0148225B2/ja
Granted legal-status Critical Current

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Landscapes

  • Porous Artificial Stone Or Porous Ceramic Products (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

〔産業上の利用分野〕 本発明は、高温用耐火断熱材、高温流体用フイ
ルター、触媒担体等に用いる少なくとも1000℃以
上の耐熱性を有するセラミツクフアイバー製の多
孔性耐火物及びその製造法に関する。 〔従来の技術〕 溶融金属の湯道、タンデイツシユ、バーナータ
イル、電気炉の内張等に用いる高温用耐火断熱
材、高温流体用フイルター、高温反応用触媒担体
等として用いるセラミツクフアイバー成形品は、
一般にSiO2繊維、Al2O3繊維、Al2O3−SiO2繊維
を、シリカゾル、アルミナゾルを含有する水中に
分散し、真空成形を行ない、乾燥した成形品を
1250〜1300℃で1〜1.5時間焼成して得ている。
しかしこれらの製品の曲げ強さ(JIS9503−1969、
5.7曲げ強さによる。以下同じ)は2〜4Kg/cm2
であつてなお充分ではない。シリカゾル、アルミ
ナゾル以外のリン酸、水ガラス等を結合剤として
用いると、繊維を劣化させ、逆に曲げ強さが低下
したり、耐熱性を低下させたりして好ましくな
い。 〔発明が解決しようとする問題点〕 本発明は上記のセラミツク繊維の耐熱性を低下
することなく、従来よりも曲げ強さの大きな成形
品からなる多孔性耐火物、及びその耐火物を安価
に得るための製造法を供せんとするものである。 〔問題点を解決するための手段〕 本発明は上記目的を達するため、SiO2繊維、
Al2O3繊維、Al2O3−SiO2繊維の一つまたは複数
からなる繊維の集合体の繊維の交差点が、主とし
てSiO2,B2O3からなる組成物で融着されている
多孔性耐火物を構成したこと、及びこれら繊維を
SiO2ゾルを含有する水中に分散し、真空成形し、
乾燥焼成を行なつた後、B2O3を溶解含有する水
溶液に浸漬し、乾燥焼成して多孔性耐火物を得る
ことにある。 〔作用〕 本発明は、上記1000℃以上の耐熱性を有する繊
維を、例えば約30〜1mm、大部分を5〜7mmの長
さにしたものを、水100重量部に対し約10重量部
以下と、シリカゾルを固形分で1〜2重量部を水
に分散し、真空成形し、乾燥した成形品を1250〜
1300℃で1〜1.5時間焼成する。繊維間に含まれ
た水が乾燥によつて蒸発し、水中に分散されてい
たシリカゾルが濃縮され、更に焼成後、繊維100
重量部に対し9〜10重量部が融着された状態にな
るようにする。次いでB2O3を水100重量部に対し
約1部溶解した硼酸水中に上記焼成した成形品を
浸漬し、引き上げて乾燥し、1250〜1300℃で1〜
1.5時間焼成する。B2O3は焼成後で繊維100重量
部に対し2〜10重量部好ましくは3〜5重量部が
結合された状態になるようにするのが良い。硼酸
は300℃でB2O3になる。B2O3の融点577℃で沸点
1500℃以上であるが、900℃頃から部分的に昇華
を始め主として繊維の交差点の隙間に集まり、シ
リカゾルによるSiO2と反応し一種の硼酸ガラス
となつて繊維の交差点を融着する。このとき繊維
中の成分の一部もこの中に溶解することがある
が、繊維の組成を変化させ、耐熱性を低下させる
ような反応は生じない。 〔実施例〕 本発明例と他の例との曲げ強さ(Kg/cm2)と、
嵩密度( )内を次表に示す。
[Industrial Application Field] The present invention relates to a porous refractory made of ceramic fiber having a heat resistance of at least 1000° C. and used for high-temperature refractory heat insulating materials, high-temperature fluid filters, catalyst carriers, etc., and a method for producing the same. [Prior art] Ceramic fiber molded products are used as high-temperature fireproof insulation materials used in molten metal runners, tundishes, burner tiles, electric furnace linings, filters for high-temperature fluids, catalyst carriers for high-temperature reactions, etc.
Generally, SiO 2 fibers, Al 2 O 3 fibers, and Al 2 O 3 -SiO 2 fibers are dispersed in water containing silica sol or alumina sol, vacuum formed, and a dried molded product is produced.
It is obtained by firing at 1250-1300°C for 1-1.5 hours.
However, the bending strength of these products (JIS9503−1969,
5.7 Depends on bending strength. (same below) is 2-4Kg/cm 2
However, it is still not enough. If phosphoric acid, water glass, or the like other than silica sol or alumina sol is used as a binder, it is undesirable because it deteriorates the fibers and conversely reduces bending strength and heat resistance. [Problems to be Solved by the Invention] The present invention provides a porous refractory made of a molded product with greater bending strength than before, and the refractory can be produced at low cost, without reducing the heat resistance of the ceramic fibers described above. The purpose of this paper is to provide a manufacturing method for obtaining the same. [Means for solving the problems] In order to achieve the above object, the present invention uses SiO 2 fibers,
A porous structure in which the intersections of the fibers of a fiber aggregate consisting of one or more of Al 2 O 3 fibers and Al 2 O 3 -SiO 2 fibers are fused with a composition mainly consisting of SiO 2 and B 2 O 3 . and that these fibers constituted a refractory.
Dispersed in water containing SiO 2 sol, vacuum formed,
After drying and firing, the material is immersed in an aqueous solution containing dissolved B 2 O 3 and then dried and fired to obtain a porous refractory. [Function] In the present invention, the above-mentioned fibers having heat resistance of 1000° C. or more are made into a length of, for example, about 30 to 1 mm, most of them 5 to 7 mm, in an amount of about 10 parts by weight or less per 100 parts by weight of water. Disperse 1 to 2 parts by weight of silica sol in water, vacuum form it, and dry the molded product.
Bake at 1300℃ for 1 to 1.5 hours. The water contained between the fibers evaporates during drying, the silica sol dispersed in the water is concentrated, and after firing, the fibers become 100%
9 to 10 parts by weight should be fused to each part by weight. Next, the fired molded product was immersed in boric acid solution containing about 1 part of B 2 O 3 per 100 parts by weight of water, taken out and dried, and heated at 1250 to 1300°C for 1 to 30 minutes.
Bake for 1.5 hours. B 2 O 3 is preferably bound in an amount of 2 to 10 parts by weight, preferably 3 to 5 parts by weight, per 100 parts by weight of fibers after firing. Boric acid turns into B 2 O 3 at 300℃. The melting point of B2O3 is 577℃ and the boiling point
Although the temperature is above 1,500℃, it begins to partially sublimate at around 900℃ and mainly collects in the gaps between the intersections of the fibers, reacts with SiO 2 produced by the silica sol, becomes a type of borate glass, and fuses the intersections of the fibers. At this time, some of the components in the fibers may also be dissolved therein, but no reaction occurs that changes the composition of the fibers or lowers their heat resistance. [Example] Bending strength (Kg/cm 2 ) of the present invention example and other examples,
The bulk density (in parentheses) is shown in the table below.

〔発明の効果〕〔Effect of the invention〕

第2図はAl2O3−SiO2繊維をシリカゾルのみを
結合剤として用い成形焼成した多孔性耐火物の電
子顕微鏡写真であるが、SiO2粒子が粒状で繊維
表面に部分的にしか融着しておらず、繊維の交差
点を結合した部分が極めて僅かである。これに対
し本発明多孔性耐火物は第1図の電子顕微鏡写真
に示すようにAl2O3−SiO2繊維の交差点を完全に
融着しており、繊維の組成も変化することなく原
状を保つていることが判る。 上表でB2O3を成分として含有するAl2O3
B2O3−SiO2繊維を使用した成形体では、SiO2
ルを結合剤として用いただけで成形体全組成中に
占めるSiO2含有量が増加するに従い曲げ強さが
増加しているが、これは焼成の際に繊維成分が反
応して低融点組成物を生じ溶融物を多量に生じて
繊維自体も溶融し収縮したことによるものであ
る。このようになると繊維のもつ耐熱性が低下し
てしまう。また従来のSiO2ゾル、Al2O3ゾルだけ
を結合剤とした場合には繊維の交差点が充分結合
されないため曲げ強さが向上せず、リン酸、水ガ
ラスを結合剤として用いたものでは、焼成によつ
て組成が変化し、繊維が劣化した。 以上本発明多孔性耐火物によれば、繊維自体の
組成を変化せず従つて繊維の耐熱性を低下させず
に、曲げ強さの大きい多孔性耐火物を提供できる
ので、取扱いに強度を必要とする高温用断熱材、
高温用フイルター、触媒担体等へ、SiO2繊維、
Al2O3繊維、Al2O3−SiO2繊維成形品の用途を拡
大できる。 また本発明製造法では、繊維の組成、用途に対
し耐火性と、曲げ強さを考慮して、結合剤として
のSiO2,B2O3の付加量を容易に調節でき、SiO2
ゾル、B2O3粉を使用して安価に強度の大きい多
孔性耐火物を提供できる。
Figure 2 is an electron micrograph of a porous refractory made by molding and firing Al 2 O 3 -SiO 2 fibers using only silica sol as a binder, but the SiO 2 particles are granular and only partially fused to the fiber surface. There are very few areas where fiber intersections are connected. In contrast, the porous refractory of the present invention completely fuses the intersections of Al 2 O 3 -SiO 2 fibers, as shown in the electron micrograph in Figure 1, and retains its original state without changing the composition of the fibers. It is clear that it is maintained. In the above table, Al 2 O 3 − containing B 2 O 3 as a component
In the molded body using B 2 O 3 −SiO 2 fibers, the bending strength increases as the SiO 2 content in the total composition of the molded body increases, even if only SiO 2 sol is used as a binder. This is because the fiber components reacted during firing to form a low melting point composition, producing a large amount of melt, and the fiber itself also melted and shrunk. When this happens, the heat resistance of the fibers decreases. Furthermore, when conventional SiO 2 sol or Al 2 O 3 sol is used as the only binder, the intersections of the fibers are not sufficiently bonded, so the bending strength does not improve, and when using phosphoric acid or water glass as the binder, , the composition changed due to firing, and the fibers deteriorated. As described above, according to the porous refractory of the present invention, it is possible to provide a porous refractory with high bending strength without changing the composition of the fiber itself and without reducing the heat resistance of the fiber. high temperature insulation material,
For high temperature filters, catalyst carriers, etc., SiO 2 fibers,
The applications of Al 2 O 3 fiber and Al 2 O 3 -SiO 2 fiber molded products can be expanded. In addition, in the production method of the present invention, the amount of SiO 2 and B 2 O 3 added as binders can be easily adjusted in consideration of the fire resistance and bending strength of the fiber composition and application.
Porous refractories with high strength can be provided at low cost using sol and B 2 O 3 powder.

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

第1図はAl2O3−SiO2繊維を用いた本発明によ
る多孔性耐火物の電子顕微鏡写真図、第2図は
Al2O3−SiO2繊維をSiO2ゾルを結合剤として成形
焼成した多孔性耐火物の電子顕微鏡写真図であ
る。
Figure 1 is an electron micrograph of a porous refractory according to the present invention using Al 2 O 3 -SiO 2 fibers, and Figure 2 is
FIG. 2 is an electron micrograph of a porous refractory obtained by molding and firing Al 2 O 3 —SiO 2 fibers using SiO 2 sol as a binder.

Claims (1)

【特許請求の範囲】 1 SiO2繊維、Al2O3繊維、Al2O3−SiO2繊維の
一つまたは複数からなる繊維集合体の繊維の交差
点が主としてSiO2,B2O3からなる組成物で融着
されていることを特徴とする多孔性耐火物。 2 SiO2繊維、Al2O3繊維、Al2O3−SiO2繊維の
一つまたは複数をSiO2ゾルを含有する水中に分
散し、真空成形し、乾燥焼成を行なつた後、
B2O3を溶解含有する水溶液に浸漬し、乾燥焼成
することを特徴とする多孔性耐火物の製造法。
[Claims] 1. The intersection of fibers in a fiber assembly consisting of one or more of SiO 2 fibers, Al 2 O 3 fibers, and Al 2 O 3 -SiO 2 fibers is mainly composed of SiO 2 and B 2 O 3 A porous refractory characterized by being fused with a composition. 2. After dispersing one or more of SiO 2 fibers, Al 2 O 3 fibers, and Al 2 O 3 -SiO 2 fibers in water containing SiO 2 sol, vacuum forming, and drying and firing,
A method for producing a porous refractory, which comprises immersing it in an aqueous solution containing dissolved B 2 O 3 and drying and firing it.
JP8574984A 1984-04-27 1984-04-27 Porous refractories and manufacture Granted JPS60231453A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8574984A JPS60231453A (en) 1984-04-27 1984-04-27 Porous refractories and manufacture

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8574984A JPS60231453A (en) 1984-04-27 1984-04-27 Porous refractories and manufacture

Publications (2)

Publication Number Publication Date
JPS60231453A JPS60231453A (en) 1985-11-18
JPH0148225B2 true JPH0148225B2 (en) 1989-10-18

Family

ID=13867497

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8574984A Granted JPS60231453A (en) 1984-04-27 1984-04-27 Porous refractories and manufacture

Country Status (1)

Country Link
JP (1) JPS60231453A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62263917A (en) * 1986-05-08 1987-11-16 Ibiden Co Ltd High heat-resistant roll
JP2583756B2 (en) * 1986-05-31 1997-02-19 イビデン株式会社 High heat resistance roll

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1417791A (en) * 1972-06-30 1975-12-17 Du Pont Fibres
JPS5163812A (en) * 1974-11-30 1976-06-02 Toyota Motor Co Ltd DANNETSUYOSERAMITSUKUSENISEIKEITAI
US4047965A (en) * 1976-05-04 1977-09-13 Minnesota Mining And Manufacturing Company Non-frangible alumina-silica fibers
JPS547359A (en) * 1977-06-17 1979-01-20 Canon Inc Dichroic film having suitable half-width
US4148962A (en) * 1978-09-08 1979-04-10 Nasa Fibrous refractory composite insulation
JPS57123604A (en) * 1981-01-23 1982-08-02 Mitsubishi Electric Corp Heat resistant composite insulator

Also Published As

Publication number Publication date
JPS60231453A (en) 1985-11-18

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