JPH0154305B2 - - Google Patents
Info
- Publication number
- JPH0154305B2 JPH0154305B2 JP28059985A JP28059985A JPH0154305B2 JP H0154305 B2 JPH0154305 B2 JP H0154305B2 JP 28059985 A JP28059985 A JP 28059985A JP 28059985 A JP28059985 A JP 28059985A JP H0154305 B2 JPH0154305 B2 JP H0154305B2
- Authority
- JP
- Japan
- Prior art keywords
- weight
- parts
- fibers
- inorganic
- bentonite
- 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
Links
- 239000000835 fiber Substances 0.000 claims description 32
- 239000012784 inorganic fiber Substances 0.000 claims description 24
- 238000001125 extrusion Methods 0.000 claims description 13
- 239000000440 bentonite Substances 0.000 claims description 12
- 229910000278 bentonite Inorganic materials 0.000 claims description 12
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 11
- 239000002994 raw material Substances 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 claims description 7
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical group [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 claims description 7
- 239000002562 thickening agent Substances 0.000 claims description 7
- 238000001035 drying Methods 0.000 claims description 5
- 238000002156 mixing Methods 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 235000012438 extruded product Nutrition 0.000 claims 1
- 239000000047 product Substances 0.000 description 21
- 238000000465 moulding Methods 0.000 description 10
- 238000000034 method Methods 0.000 description 8
- 239000000919 ceramic Substances 0.000 description 6
- 238000004901 spalling Methods 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 238000010304 firing Methods 0.000 description 3
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 238000007665 sagging Methods 0.000 description 2
- 238000007666 vacuum forming Methods 0.000 description 2
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 241001502129 Mullus Species 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000010427 ball clay Substances 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- KZHJGOXRZJKJNY-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Si]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O KZHJGOXRZJKJNY-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000007580 dry-mixing Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000011094 fiberboard Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000009970 fire resistant effect Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 239000002557 mineral fiber Substances 0.000 description 1
- 229910052863 mullite Inorganic materials 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000011819 refractory material Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000012798 spherical particle Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
Landscapes
- Porous Artificial Stone Or Porous Ceramic Products (AREA)
Description
〔産業上の利用分野〕
本発明は無機繊維を含有する耐火性の成形品、
特に、ガラスタンク窯のバツクアツプ材、陶磁器
焼成用セツター、製鋼用取鍋及びタンデイシユ等
の耐スケール性、耐風速性などが重視される用途
に適する無機繊維質成形品の押出成形に関する。
〔従来の技術〕
無機繊維質の成形品を製造する場合、一般的に
は真空成形法が広く使用されている。この方法
は、無機繊維バルクをチヨツプした短繊維を無機
又は有機バインダーと共に水中に分散させてスラ
リー状とした後、細かい網などで構成した濾過式
型を用いて真空吸引し、網の表面に堆積した無機
繊維層を脱型し、乾燥して成形品するものであ
る。しかしこの方法では、無機繊維の保有する圧
縮復元性を殆んど抑制していないため、完成品の
密度は0.1〜0.3Kg/と比較的軽量となり、断熱
性には優れているものの強度的には不充分であ
る。従つて、係る成形品は一般に余り強度の要求
されない用途に施工方法を工夫しながら使用され
ている。
しかし、用途によつては施工方法のみで無機繊
維質成形品の強度を補うことは難かしく、例えば
ガラスタンク窯のバツクアツプ材、陶磁器焼成用
セツター、製鋼用の取鍋やタンデイシユ等の用途
には従来の無機繊維質成形品は使用できず、無機
繊維のもつ断熱性、耐スポーリング性と、耐火物
のもつ高強度の両方を合わせもつ製品の開発が望
まれていた。
このような高強度の無機繊維質成形品を製造す
るために現在、プレス成形法又は鋳込成形法が少
量ではあるが実施されている。しかし、いずれの
方法においても、成形後のタレ、変形を防止する
ために極力水分量を減らす必要があり、時には原
料組成物を半乾燥状態に調整する必要がある。こ
のような高濃度では繊維が互にからみ合つて均一
に分散、混合されずそのまゝ成形されてしまうの
で、得られた成形品は密度の不均一や強度のアン
バランスを生じ易く、且つバツチ式であるため製
造能率も低い等の欠点があつた。
このようなプレス成形法や鋳込成形法に代えて
押出成形法も検討されているが、無機繊維は非可
塑性原料であると云うだけでなく、スポンジのよ
うに外圧を加えると簡単にへこむが、外圧が解放
されると殆んど元の状態にまで復元する性質を有
するため、無機繊維の多い原料組成物の押出成形
は不可能であると考えられてきた。
〔発明が解決しようとするする問題点〕
本発明は従来不可能とされていた、無機繊維質
原料を押出成形法によつて高品質の成形品を連続
的に製造する方法を提供することを目的とする。
〔問題点を解決するための手段〕
上記目的を達成するために、本発明者は無機繊
維の可塑化に関して鋭意研究を行ない、本発明に
至つたものであり、その無機繊維質押出成形品の
製造方法は実質繊維重量部が100重量部の、平均
繊維径1〜10μm及び平均繊維長0.5〜20mmの無機
繊維に、24〜50重量部のベントナイト、0.6〜3.2
重量部の増粘剤及び120〜360重量部の水を添加混
合し、混合原料組成物を押出成形し、乾燥するこ
とを特徴とする。
本発明に用いられる無機繊維は、一般にセラミ
ツクフアイバーと呼ばれるアルミノシリケートフ
アイバー、アルミナフアイバー、ムライトフアイ
バー、ジルコニアフアイバー、アルミノボロシリ
ケートフアイバー、シリカフアイバー、ミネラル
フアイバー等であり、成形品の用途に応じて一種
又は二種以上を適宜選択できる。
無機繊維は予めハンマークラツシヤ、デシンタ
ー等で破砕し、平均繊維径1〜10μm及び平均繊
維長0.5〜20mmとする。
無機繊維を押出成形に適するように可塑化する
ための塑性原料としてはベントナイトを使用す
る。ベントナイトは均一な混合を達成するために
乾燥微粉として無機繊維に添加するのが好まし
い。カオリン、ボールクレー等の他の粘土類は大
量に配合しないと無機繊維の可塑化に有効でな
く、このため得られる成形品は高密度となり良好
な耐スポーリング性が得られない。又、強度改善
のために一般に用いられているバインダーは繊維
の特徴を失なわない程度に少量使用することがで
きるが、コロイダルシリカは成形後の乾燥時に成
形品の表面部に移行し、特に硬質ボードの場合に
表面亀裂の原因となるので使用を避けるのが好ま
しい。
脱粘剤としては、ポリアクリル酸ソーダ、ポリ
ビニルアルコール、カルボキシメチルセルロー
ス、メチルセルロース、ヒドロキシエチルセルロ
ース等を使用でき、ポリアクリル酸ソーダが好ま
しい。増粘剤は0.5〜1.0%程度の低濃度水溶液と
し、特に添加配合すべき全量の水を増粘剤水溶液
として供給すると便利である。
各原料の配合は、無機繊維とベントナイトとを
1〜60分間乾式混合し、更に増粘剤水溶液を加え
て1〜60分間混合する。混合機については、マラ
ー型、リボン型、スクリユー式等の混合機を使用
できるが、混合完了後少なくとも24時間放置して
から押出成形すると、成形自体が容易であるばか
りか、品質的にも良好である。押出成形後は直ち
に乾燥しても問題はなく、乾燥にも特別な条件は
ない。又、必要に応じて乾燥後に焼成処理を行な
うこともできる。
〔作用〕
無機繊維はその平均繊維径が10μmを超えると
混練度合によつて嵩密度にバラツキを生じ、成形
品の強度、耐スポーリング性が低下するので、
10μm以下が適当であり、5μm以下が好ましい。
又、平均繊維長が20mmを超えると繊維の分散が悪
くなり、やはり嵩密度にバラツキを生じて、成形
品の強度、耐スポーリング性が悪化するので、20
mm以下が適当であり、10μm以下が好ましい。
実質繊維重量部が100重量部の無機繊維に対し
て、ベントナイトが24重量部未満では可塑性が不
足し、押出成形が困難であり、50重量部を超える
と成形時のタレや変形、乾燥時の収縮や亀裂など
が発生し、又嵩密度が大きくなり耐スポーリング
性が失なわれ、成形品の耐熱性も低下する。ベン
トナイトの配合量を比較的少量に抑える代りに
0.6〜3.2重量部の増粘剤を使用するが、増粘剤が
3.2重量部を超えると成形時のタレや変形、乾燥
時の亀裂などが発生しやすく、0.6重量部未満で
は押出成形が困難であり、例え成形できても成形
能率が著しく低下する。
なお、実質繊維重量部とは、無機繊維中に存在
する非繊維質球状粒子(シヨツト)を除外した実
質繊維部分の重量部を意味する。
〔実施例〕
実施例 1〜8
平均繊維径2.8μm、組成Al2O347%―SiO252%
―酸化物1%のセラミツクフアイバー(イソライ
ト・バブコツク耐火(株)製の商品名カオウール)を
ハンマークラツシヤーで平均繊維長4〜10mmとし
たもの180重量部(実質繊維重量部で100重量部)
に、ベントナイト28重量部をマラー型混合機で3
分間乾式混合し、更にポリアクリル酸ソーダの
0.5%水溶液280重量部を加えて5分間混合した。
混合原料組成物を48時間ねかした後、真空押出成
形機により長さ600mm×幅300mm×厚さ20mmのボー
ドを成形し、直ちに乾燥処理してセラミツクフア
イバー質の硬質ボードを得た。この製品の品質は
下記第1表に示す他、灼熱減量1.6%、、熱伝導率
0.17Kcal/mh℃(平均温度600℃)であつた。
この実施例1と同様にして、但しベントナイト
及びポリアクリル酸ソーダの配合量を変えて、実
施例2〜8及び比較例1〜3を実施し、その配合
及び品質を第1表に示した。
[Industrial Application Field] The present invention provides a fire-resistant molded article containing inorganic fibers,
In particular, the present invention relates to extrusion molding of inorganic fiber molded products suitable for applications where scale resistance, wind speed resistance, etc. are important, such as backup materials for glass tank kilns, setters for ceramic firing, ladles and tundishes for steel manufacturing. [Prior Art] When manufacturing inorganic fiber molded articles, vacuum forming methods are generally widely used. In this method, short fibers obtained by chopping bulk inorganic fibers are dispersed in water together with an inorganic or organic binder to form a slurry, which is then vacuum-suctioned using a filtration mold made of fine mesh, and deposited on the surface of the mesh. The inorganic fiber layer is removed from the mold and dried to form a molded product. However, this method hardly suppresses the compressive recovery properties of inorganic fibers, so the density of the finished product is relatively light at 0.1 to 0.3 kg/, and although it has excellent heat insulation properties, it has poor strength. is insufficient. Therefore, such molded products are generally used for applications that do not require much strength, while devising a construction method. However, depending on the application, it may be difficult to supplement the strength of inorganic fiber molded products through construction methods alone. Conventional inorganic fiber molded products could not be used, and there was a desire to develop a product that combines the heat insulation and spalling resistance of inorganic fibers with the high strength of refractories. In order to produce such high-strength inorganic fibrous molded products, press molding or cast molding methods are currently being used, albeit in small quantities. However, in either method, it is necessary to reduce the moisture content as much as possible to prevent sagging and deformation after molding, and it is sometimes necessary to adjust the raw material composition to a semi-dry state. At such a high concentration, the fibers become entangled with each other and are not evenly dispersed or mixed and are molded as they are, so the resulting molded product is likely to have uneven density and unbalanced strength. Since it is a formula, it has drawbacks such as low manufacturing efficiency. Extrusion molding methods are being considered as an alternative to such press molding and cast molding methods, but inorganic fibers are not only non-plastic raw materials, but also like sponges, they easily dent when external pressure is applied. It has been thought that extrusion molding of a raw material composition containing a large amount of inorganic fibers is impossible because it has the property of restoring to almost its original state when external pressure is released. [Problems to be Solved by the Invention] The present invention aims to provide a method for continuously manufacturing high-quality molded products from inorganic fibrous raw materials by extrusion molding, which was previously considered impossible. purpose. [Means for Solving the Problems] In order to achieve the above object, the present inventor has conducted intensive research on the plasticization of inorganic fibers, and has arrived at the present invention. The production method is to add 100 parts by weight of actual fibers to inorganic fibers with an average fiber diameter of 1 to 10 μm and an average fiber length of 0.5 to 20 mm, 24 to 50 parts by weight of bentonite, and 0.6 to 3.2 parts by weight of bentonite.
It is characterized in that parts by weight of a thickener and 120 to 360 parts by weight of water are added and mixed, the mixed raw material composition is extruded, and then dried. The inorganic fibers used in the present invention include aluminosilicate fibers, which are generally called ceramic fibers, alumina fibers, mullite fibers, zirconia fibers, aluminoborosilicate fibers, silica fibers, and mineral fibers, depending on the purpose of the molded product. Two or more types can be selected as appropriate. The inorganic fibers are crushed in advance using a hammer crusher, de-sinter, etc. to give an average fiber diameter of 1 to 10 μm and an average fiber length of 0.5 to 20 mm. Bentonite is used as a plastic raw material for plasticizing inorganic fibers to make them suitable for extrusion molding. Bentonite is preferably added to the inorganic fibers as a dry fine powder to achieve uniform mixing. Other clays such as kaolin and ball clay are not effective in plasticizing inorganic fibers unless they are blended in large quantities, and therefore the resulting molded product has a high density and does not have good spalling resistance. Furthermore, binders that are commonly used to improve strength can be used in small amounts without losing the characteristics of the fibers, but colloidal silica migrates to the surface of the molded product when it dries after molding, making it especially hard. In the case of boards, it is preferable to avoid its use as it may cause surface cracks. As the deviscosity agent, sodium polyacrylate, polyvinyl alcohol, carboxymethyl cellulose, methyl cellulose, hydroxyethyl cellulose, etc. can be used, and sodium polyacrylate is preferred. The thickener is a low concentration aqueous solution of about 0.5 to 1.0%, and it is especially convenient to supply the entire amount of water to be added and blended as the thickener aqueous solution. The raw materials are mixed by dry mixing the inorganic fibers and bentonite for 1 to 60 minutes, and then adding an aqueous thickener solution and mixing for 1 to 60 minutes. As for the mixer, you can use a mullet type, ribbon type, or screw type mixer, but if you leave it for at least 24 hours after mixing is completed, then extrusion molding will not only make the molding itself easier, but also improve the quality. It is. There is no problem in drying immediately after extrusion molding, and there are no special conditions for drying. Further, a firing treatment can be performed after drying if necessary. [Function] If the average fiber diameter of inorganic fibers exceeds 10 μm, the bulk density will vary depending on the degree of kneading, and the strength and spalling resistance of the molded product will decrease.
The thickness is suitably 10 μm or less, preferably 5 μm or less.
In addition, if the average fiber length exceeds 20 mm, the dispersion of the fibers will deteriorate, resulting in variations in bulk density and deteriorating the strength and spalling resistance of the molded product.
mm or less is appropriate, and 10 μm or less is preferable. If the bentonite content is less than 24 parts by weight for an inorganic fiber with an actual fiber weight part of 100 parts by weight, the plasticity will be insufficient and extrusion molding will be difficult. Shrinkage and cracks occur, bulk density increases, spalling resistance is lost, and the heat resistance of the molded product also decreases. Instead of keeping the amount of bentonite to a relatively small amount,
Use 0.6 to 3.2 parts by weight of thickener, but if the thickener
If it exceeds 3.2 parts by weight, sagging and deformation during molding and cracking during drying are likely to occur, while if it is less than 0.6 parts by weight, extrusion molding is difficult, and even if molding is possible, the molding efficiency will be significantly reduced. Note that the weight part of real fiber means the weight part of the real fiber portion excluding non-fibrous spherical particles (shot) present in the inorganic fiber. [Example] Examples 1 to 8 Average fiber diameter 2.8 μm, composition Al 2 O 3 47% - SiO 2 52%
- Ceramic fiber containing 1% oxide (trade name: Kao Wool, manufactured by Isolite Babkotsu Fireproofing Co., Ltd.) with an average fiber length of 4 to 10 mm using a hammer crusher, 180 parts by weight (100 parts by weight of actual fiber)
Then, 28 parts by weight of bentonite was mixed with 3 parts by weight in a Muller type mixer.
Dry mix for 1 minute, then add sodium polyacrylate.
280 parts by weight of a 0.5% aqueous solution was added and mixed for 5 minutes.
After the mixed raw material composition was left to rest for 48 hours, a board with a length of 600 mm x width of 300 mm x thickness of 20 mm was formed using a vacuum extrusion molding machine, and immediately dried to obtain a hard ceramic fiber board. The quality of this product is shown in Table 1 below, as well as ignition loss of 1.6%, and thermal conductivity.
It was 0.17Kcal/mh℃ (average temperature 600℃). Examples 2 to 8 and Comparative Examples 1 to 3 were carried out in the same manner as Example 1, except that the amounts of bentonite and sodium polyacrylate were changed, and the formulations and qualities are shown in Table 1.
【表】
実施例 9〜11
実施例1と同一のセラミツクフアイバーをデシ
ンターで平均繊維長2〜7mmとしたもの180重量
部(実質繊維重量部で100重量部)に、ベントナ
イト26重量部を乾式混合し、ポリアクリル酸ソー
ダの0.5%水溶液180重量部を加えて混合した。混
合原料組成物を48時間ねかした後、真空成形機に
より外径40mm×内径30mm×長さ300mmの円筒を成
形し、乾燥してセラミツクフアイバー質の硬質ス
リーブを製造した。この製品の品質は下記第2表
に示す他、灼熱減量1.6%、圧縮強度が常温で
23.6Kg/cm2及び1000℃×24h焼成後40Kg/cm2であ
つた。
この実施例9と同様にして、但しベントナイト
及びポリアクリル酸ソーダの配合量を変えて、実
施例10〜11及び比較例4〜7を実施し、その配合
及び品質を第2表に示した。[Table] Examples 9 to 11 26 parts by weight of bentonite was dry mixed with 180 parts by weight (100 parts by weight of actual fibers) of the same ceramic fiber as in Example 1 with an average fiber length of 2 to 7 mm using a de-sinter. Then, 180 parts by weight of a 0.5% aqueous solution of sodium polyacrylate was added and mixed. After the mixed raw material composition was left to rest for 48 hours, it was molded into a cylinder with an outer diameter of 40 mm x an inner diameter of 30 mm x a length of 300 mm using a vacuum forming machine, and dried to produce a hard ceramic fiber sleeve. The quality of this product is shown in Table 2 below, as well as a loss on burning of 1.6% and a compressive strength at room temperature.
The weight was 23.6Kg/cm 2 and 40Kg/cm 2 after firing at 1000°C for 24 hours. Examples 10 to 11 and Comparative Examples 4 to 7 were carried out in the same manner as Example 9, except that the amounts of bentonite and sodium polyacrylate were changed, and the formulations and qualities are shown in Table 2.
本発明によつて、無機繊維質成形品を押出成形
法により連続的に効率良く製造することが可能と
なり、得られる無機繊維質押出成形品は耐熱性、
耐スポーリング性と、高強度とを合わせ具えたも
のであつて、耐スケール性及び耐風速性等が重視
される用途に充分使用可能であり、無機繊維質製
品の応用範囲を拡大するものである。
According to the present invention, it is possible to continuously and efficiently manufacture inorganic fibrous molded products by extrusion molding, and the obtained inorganic fibrous extrusion molded products have heat resistance,
It has both spalling resistance and high strength, and can be fully used in applications where scale resistance and wind speed resistance are important, expanding the range of applications for inorganic fiber products. be.
Claims (1)
1〜10μm及び平均繊維長0.5〜20mmの無機繊維
に、24〜50重量部のベントナイト、0.6〜3.2重量
部の増粘剤及び120〜360重量部の水を添加混合
し、混合原料組成物を押出成形し、乾燥すること
を特徴とする、無機繊維質押出成形品の製造方
法。 2 上記増粘剤がポリアクリル酸ソーダであるこ
とを特徴とする、特許請求の範囲1項記載の無機
繊維質押出成形品の製造方法。[Scope of Claims] 1. Inorganic fibers having an average fiber diameter of 1 to 10 μm and an average fiber length of 0.5 to 20 mm, with an actual fiber weight part of 100 parts by weight, 24 to 50 parts by weight of bentonite, and an addition of 0.6 to 3.2 parts by weight. A method for producing an inorganic fibrous extruded product, which comprises adding and mixing a sticky agent and 120 to 360 parts by weight of water, extruding a mixed raw material composition, and drying the mixture. 2. The method for producing an inorganic fibrous extrusion molded product according to claim 1, wherein the thickener is sodium polyacrylate.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP28059985A JPS62143883A (en) | 1985-12-13 | 1985-12-13 | Manufacture of inorganic fiber extrusion molded product |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP28059985A JPS62143883A (en) | 1985-12-13 | 1985-12-13 | Manufacture of inorganic fiber extrusion molded product |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62143883A JPS62143883A (en) | 1987-06-27 |
| JPH0154305B2 true JPH0154305B2 (en) | 1989-11-17 |
Family
ID=17627276
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP28059985A Granted JPS62143883A (en) | 1985-12-13 | 1985-12-13 | Manufacture of inorganic fiber extrusion molded product |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS62143883A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH01148764A (en) * | 1987-12-03 | 1989-06-12 | Nichias Corp | Lightweight refractories and their manufacturing method |
| JPH01148765A (en) * | 1987-12-07 | 1989-06-12 | Nichias Corp | Lightweight refractories and their manufacturing method |
| JP2614809B2 (en) * | 1993-03-26 | 1997-05-28 | ニチアス株式会社 | Manufacturing method of heat-resistant low specific gravity fibrous molding |
-
1985
- 1985-12-13 JP JP28059985A patent/JPS62143883A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62143883A (en) | 1987-06-27 |
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