JPS593082A - Manufacture of refractories impregnated with surfactant or water-soluble organic matter - Google Patents

Manufacture of refractories impregnated with surfactant or water-soluble organic matter

Info

Publication number
JPS593082A
JPS593082A JP57108522A JP10852282A JPS593082A JP S593082 A JPS593082 A JP S593082A JP 57108522 A JP57108522 A JP 57108522A JP 10852282 A JP10852282 A JP 10852282A JP S593082 A JPS593082 A JP S593082A
Authority
JP
Japan
Prior art keywords
water
surfactant
refractory
soluble organic
refractories
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
JP57108522A
Other languages
Japanese (ja)
Other versions
JPH0235710B2 (en
Inventor
護郎 佐藤
悠策 有馬
広泰 西田
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.)
JGC Catalysts and Chemicals Ltd
Original Assignee
Catalysts and Chemicals Industries 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 Catalysts and Chemicals Industries Co Ltd filed Critical Catalysts and Chemicals Industries Co Ltd
Priority to JP57108522A priority Critical patent/JPS593082A/en
Publication of JPS593082A publication Critical patent/JPS593082A/en
Publication of JPH0235710B2 publication Critical patent/JPH0235710B2/ja
Granted legal-status Critical Current

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Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本発明は、耐火材料粉末単独または耐火材料粉末と粘結
剤を成形して得られる成形物を乾燥または焼成する耐火
物の製造法を改良し、強度的に優れた耐火物を創造する
方法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention improves a method for producing refractories by drying or firing a molded product obtained by molding a refractory material powder alone or a refractory material powder and a binder. It concerns a method of creating refractories.

本発明において耐火物とは、熱の急激な変化に耐え、同
時に機械的強さが十分であるばかシでなく、これと接触
するガラス、溶融体、固体などの侵食、庫滅などに抵抗
性のあるものを云い、これには定形耐火物、不定形耐火
物を始めとして精密鋳造業界における鋳型が包含される
In the present invention, a refractory is defined as a material that can withstand sudden changes in heat, has sufficient mechanical strength, and is resistant to erosion and deterioration of glass, molten material, solid materials, etc. that come into contact with it. This includes molds used in the precision casting industry, including shaped refractories and monolithic refractories.

従来、比較的強度の良い耐火物を製造する方法としては
、コロイド状シリカ液等の適当な粘結剤を選択して使う
方法、耐火材料粉末の粒度分布を調整して用いる方法、
ガラス繊維等のような補強材を添加する方法およびこれ
らを組合せる方法など種々方法が検討されているが、お
のおの作業性または耐火物強度の面で不充分である。耐
火物の粘結剤としてはコロイド状シリカ液が多く使用さ
れており、精密鋳造用には不純物の少ないものが良く使
われているが、コロイド状シリカ液と耐火材料粉末のみ
を混練した場合KFi、耐火材料の吸水によるコロイド
状シリカ液の部分ゲル化が起りやすく、これが起ると均
一々混練ができないため、充分な強度の耐火物を得るこ
とが困難であった。コロイド状シリカ液以外の粘結剤に
ついて言えば、エチルシリケート、リン酸塩、ケイ酸塩
等のような種々のものが使われているが、これらは有機
物やアルカリ金属等好ましくないものの含有量が多いた
め、耐火物製造時の作業性が悪く、得られた耐火物は強
度の熱的変化が大きく、その品質管理も難しい。
Conventionally, methods for manufacturing refractories with relatively good strength include selecting and using an appropriate binder such as colloidal silica liquid, adjusting the particle size distribution of refractory material powder,
Various methods have been studied, such as adding reinforcing materials such as glass fibers and combining these methods, but each method is insufficient in terms of workability or refractory strength. Colloidal silica liquid is often used as a binder for refractories, and those with few impurities are often used for precision casting, but when only colloidal silica liquid and refractory material powder are kneaded, KFi Partial gelation of the colloidal silica liquid tends to occur due to water absorption by the refractory material, and when this occurs, uniform kneading cannot be achieved, making it difficult to obtain a refractory with sufficient strength. As for binders other than colloidal silica liquid, various binders such as ethyl silicate, phosphates, silicates, etc. are used, but these contain undesirable substances such as organic substances and alkali metals. Because of this large amount, workability during refractory production is poor, and the resulting refractories exhibit large thermal changes in strength, making quality control difficult.

一方、耐火材料粉末やガラス繊維々どを選択して使用す
ることは、その耐火材料の有する熱膨張率、結晶形、粒
度分布などの性質により耐火物の強度が大きく異なるこ
とから、再現性のある耐火物を得ることが帷しく、作業
の面でも細心の注意と管理が必要である。
On the other hand, selecting and using refractory material powders and glass fibers is difficult because the strength of the refractory varies greatly depending on the properties of the refractory material, such as its coefficient of thermal expansion, crystal shape, and particle size distribution. Obtaining certain refractories is difficult, and the work requires careful attention and management.

本発明は、これらの耐火物を製造する方法の欠点を解消
し、よシ優れた耐火物の製造方法を提供せんとするもの
であって、その特徴とするところは従来から鋳造業界で
一般的に採用されている方法、すなわち耐火材料粉末単
独または耐火材料粉末と粘結剤を成形し、得られた成形
物を乾燥し、必要に応じて焼成することからなる耐火物
の製造方法において、乾燥または焼成後の骸成形物に、
コロイド状シリカ液と界面活性剤または水溶性有機物と
からなる含浸液を含浸させ、必要に心して乾燥または焼
成することにある。従って、本発明の方法によれば、適
当な混線装置に耐火材料粉末または耐火材料粉末と粘結
剤を入れ、水を加えて適当な水分に調整して混練し、そ
の混線物を成形して乾燥し、必要に応じてさらに焼成し
てまず成形物を調製する。次いで#キ*≠≠この成形物
にコロイド状シリカ液と界面活性剤または水溶性有機物
との混合液を含浸させ、しかる後乾燥または焼成するこ
とによって、目的とする耐火物を製造することができる
The present invention aims to eliminate the drawbacks of these methods of manufacturing refractories and provide a more excellent method of manufacturing refractories, which is characterized by the same characteristics that have been conventionally used in the casting industry. In the refractory production method, which consists of molding a refractory material powder alone or a refractory material powder and a binder, drying the obtained molded product, and firing it as necessary, Or to the skeleton molded product after firing,
The method consists of impregnating a colloidal silica liquid with an impregnating liquid consisting of a surfactant or a water-soluble organic substance, and drying or baking as necessary. Therefore, according to the method of the present invention, a refractory material powder or a refractory material powder and a binder are put into a suitable mixing device, water is added to adjust the moisture to an appropriate level, the mixture is kneaded, and the mixed material is molded. First, a molded article is prepared by drying and further firing if necessary. Next, #ki*≠≠The desired refractory can be manufactured by impregnating this molded product with a mixed solution of colloidal silica liquid and a surfactant or water-soluble organic substance, and then drying or baking it. .

本発明で使用される耐火材料と11、では、ガラス状シ
リカ、結晶シリカ、ケイ酸マグネシウム、ケイ酸アルミ
ニウム、ケイ酸ジルコニウム、ケイ酸粘土、電融シリカ
等のケイ酸質の酸性耐火物の他、マグネシア、ドロマイ
ト、マグクロ等の塩基性耐火物、酸化クロム、クロマイ
ト尋の中性耐火物、炭素、炭化ケイ素、ジルコニア等の
特殊耐火物などが例示できる。
The refractory materials used in the present invention and 11 include silicic acidic refractories such as glassy silica, crystalline silica, magnesium silicate, aluminum silicate, zirconium silicate, silicate clay, and fused silica. Examples include basic refractories such as magnesia, dolomite, and maguro, neutral refractories such as chromium oxide and chromite, and special refractories such as carbon, silicon carbide, and zirconia.

また、コロイド状シリカ液としては、如何なる方法で製
造されたものでも使用可能であって、例えば、イオン交
換法、解膠法、透析法などの方法で製造されたものが本
発明で使用できる。
Further, as the colloidal silica liquid, one produced by any method can be used, and for example, one produced by a method such as an ion exchange method, a peptization method, or a dialysis method can be used in the present invention.

コロイド状シリカ液のシリカの平均粒子径は6′“〜5
0ミリミクロンの範囲が適当であるが、特に6〜1B$
り電クロンの範囲の屯のが好ましい、また、シリカ濃度
はSIO!と[7て15重量、e−セント以上のものが
経済的で好都合である。
The average particle size of silica in colloidal silica liquid is 6'"~5
A range of 0 millimicrons is suitable, but especially 6 to 1 B$
It is preferable that the silica concentration be in the range of 2000m, and the silica concentration should be in the range of SIO! It is economical and convenient to have a weight of 7 to 15 e-cents or more.

′コロイド状シリカ液と混合する界面活性剤または水溶
性有機物は、コロイド状シリカ液とゲル化を起さないこ
とが必要である。界面活性剤としては、アニオン系また
は非イオン系のものであれば良く、その中で特にジアル
キルスルフオサクシネート、高アルコ−、ルサルフエー
ト(Na塩)等のアニオン系活性剤とポリオキシエチレ
ンアルキルフェニルエーテル等の非イオン系活性剤が好
ましい。本発明に適する界面活性剤を商品名で例示すれ
ば、アニオン系活性剤とL−’li:、ネオコール、ペ
レックスOT、 tンモリンOT、セドラン尋が、非イ
オン系活性剤としては、ノニボールB等がある。
'The surfactant or water-soluble organic substance mixed with the colloidal silica liquid must not cause gelation with the colloidal silica liquid. The surfactant may be an anionic or nonionic surfactant, especially anionic surfactants such as dialkyl sulfosuccinate, high alcohol, rusulfate (Na salt), and polyoxyethylene alkylphenyl. Nonionic activators such as ethers are preferred. Examples of surfactants suitable for the present invention by trade name include anionic surfactants such as L-'li:, Neocol, Perex OT, Tonmorin OT, and Cedran Hiro; examples of nonionic surfactants include Noniball B, etc. There is.

一方、水溶性有機物としては、水に可溶な有機物であれ
ばいずれも使用可能であって、例えば、メチルア化コー
ル、エチルアルコール等ノアルコール類、アセトン、メ
チルエチルケトン等のケトン類、メチルアミン、メチル
アミン等の一級アミン類、エチレングリコール、グリセ
リン等の多価アルコール類が使用される。これらの中で
特にメチルアルコール、エチルアルコール等のアルコー
ル類及び、アセトン等のケトン類の使用が経済的で都合
がよい。
On the other hand, as the water-soluble organic substance, any organic substance that is soluble in water can be used, such as alcohols such as methylated alcohol, ethyl alcohol, ketones such as acetone and methyl ethyl ketone, methylamine, Primary amines such as amines and polyhydric alcohols such as ethylene glycol and glycerin are used. Among these, it is especially economical and convenient to use alcohols such as methyl alcohol and ethyl alcohol, and ketones such as acetone.

コロイド状シリカ液と上述の界面活性剤または水溶性有
機物の混合組成は、Sing乾燥重1゛対界面活性剤重
量または水溶性有機物重量の比が100:0.5から3
00:20  の範囲、好ましくは100:2からZo
oニアの範囲になるよう混合することを可とする。
The mixed composition of colloidal silica liquid and the above-mentioned surfactant or water-soluble organic substance has a ratio of Sing dry weight 1゜ to surfactant weight or water-soluble organic substance weight of 100:0.5 to 3.
00:20, preferably 100:2 to Zo
It is possible to mix it so that it is within the range of o.

なお、含浸液の耐火物への含浸割合はコロイド状シリカ
液の810.乾燥重量対耐火物の重量の比で0.05:
100から1.0:Zooの範囲であれば良いが、0.
1:100から0.3:100の範囲が作業性、経済性
の面で適当である。また、含浸液の耐火物への含浸方法
忙は耐火物を含浸液の中に浸漬する方法、浸漬後加圧も
しくは減圧して行なう方法等いかなる含浸方法を用いて
もかまわない。このようにして含浸処理を受けた成形物
は必要に応じ業界周知の方法で乾燥または焼成される。
The impregnating ratio of the impregnating liquid into the refractory is 810% of the colloidal silica liquid. Ratio of dry weight to weight of refractory: 0.05:
A range of 100 to 1.0:Zoo is fine, but 0.
A range of 1:100 to 0.3:100 is appropriate in terms of workability and economy. Further, any impregnation method may be used for impregnating the refractory with the impregnating liquid, such as a method in which the refractory is immersed in the impregnating liquid, or a method in which the refractory is pressurized or depressurized after immersion. The molded product thus impregnated is dried or fired, if necessary, by methods well known in the industry.

実施例1 耐火材料粉末としてジルコンサンド及びジルコンフラワ
ーを使用し7、粘結剤を用いることなく加圧成形法にて
円柱状成形物を作製し、該成形物を48時間室温にて風
乾後、110℃で20時間乾燥させ、デシケータ中で冷
却したものを含浸用テストピースとした。このものの重
量は75fであった。
Example 1 Using zircon sand and zircon flour as refractory material powder7, a cylindrical molded product was produced by pressure molding without using a binder, and after air-drying the molded product at room temperature for 48 hours, The test piece was dried at 110° C. for 20 hours and cooled in a desiccator to prepare a test piece for impregnation. The weight of this item was 75f.

8i0.濃度30重量パーセント、Nano濃度0゜4
2重量/R−セント、pH9,5、平均粒子径12ミリ
きクロンのコロイド状シリカ液(商品名カタロイドー5
I30)66.2Fとアニオン系活性剤(商品名セドラ
ン)IFと水32.2 f混合して本発明の含浸液を調
製した。との含浸液の中に上述の含浸用テストピースを
53分間浸漬した後、テストピースを取り出し時の重量
は81. Ofであった。その後xxotzo時間乾燥
させ、さらに900℃1時間焼成し1、デシケータ中に
て冷却した後、圧縮破壊強度を測定した。強度測定はJ
I8 R−2206−19155に則9、加圧破壊時の
荷重を測定する方法で行なった。その結果を表−1に示
す。
8i0. Concentration: 30% by weight, Nano concentration: 0°4
2 weight/R-cent, pH 9.5, average particle size 12 mm colloidal silica liquid (trade name Cataloid-5)
The impregnating liquid of the present invention was prepared by mixing 66.2 F of I30), an anionic activator (trade name: CEDRAN) IF, and 32.2 F of water. After the above-mentioned test piece for impregnation was immersed in the impregnating liquid for 53 minutes, the weight when taken out was 81. It was Of. Thereafter, it was dried for xxotzo hours, further calcined at 900°C for 1 hour, and after cooling in a desiccator, the compressive fracture strength was measured. Strength measurement is J
The test was carried out in accordance with I8 R-2206-19155, 9, and the method of measuring the load at the time of pressure fracture. The results are shown in Table-1.

実施例2 実施例1と同じコロイド状シリカ液66.2 fとアニ
オン系活性剤(商品名セドラン) 0.012と水32
.2 Fを混合して含浸液をPJ14製した。
Example 2 The same colloidal silica liquid as in Example 1 66.2 f, anionic activator (trade name: Cedran) 0.012 and water 32
.. 2F was mixed to prepare an impregnating liquid PJ14.

この含浸液を実施例1と同様含浸用テストぎ一スに含浸
させ、さらに同じ乾燥、焼成処理を施したものの圧縮破
壊強度を測定した。その結果を表−1に示す。
An impregnating test piece was impregnated with this impregnating solution in the same manner as in Example 1, and then subjected to the same drying and firing treatment, and its compressive fracture strength was measured. The results are shown in Table-1.

実施例3 実施例1と同じコロイド状シリカ液33.4 fとアニ
オン系活性剤(商品名セドラン)IPと水65、Ofを
混合して含浸液を調製した。実施例1と同様に、との含
浸液を含浸用テストピースに含浸させ、さらに同じ乾燥
、焼成処理を施したものの圧縮破壊強度を測定した。そ
の結果を衷−1に示す。
Example 3 An impregnating liquid was prepared by mixing 33.4 f of the same colloidal silica liquid as in Example 1, an anionic activator (trade name: Cedran) IP, and 65.5 f of water. In the same manner as in Example 1, an impregnating test piece was impregnated with the impregnating solution and subjected to the same drying and firing treatment, and the compressive fracture strength was measured. The results are shown in Figure 1.

実施例4 実施例オと同じコロイド状シリカ液66.2 fとメチ
ルアルコール(99チ純度)1fと水32、2 Fを混
合して含浸液を調製した。実施例1と同様、この含浸液
を含浸用テスト2−スに含浸させ、さらに同じ乾燥、焼
成処理を施したものについて圧縮破壊強度を測定した。
Example 4 An impregnating solution was prepared by mixing 66.2 f of the same colloidal silica liquid as in Example E, 1 f of methyl alcohol (99% purity), and 32.2 F of water. As in Example 1, this impregnating liquid was impregnated into the impregnating test 2-space, which was further subjected to the same drying and firing treatment, and the compressive fracture strength was measured.

その結果を表−IK示す。The results are shown in Table IK.

(以丁余白) 表−1 なお、圧縮破壊強度は、成形物テストピース3個の平均
値である。
(Additional margin) Table 1 The compressive breaking strength is the average value of three molded test pieces.

以上説明したように、耐火材料粉末または耐火材料粉末
と粘結材を成形して得られる成形物を乾燥または焼成す
ることからなる耐火物の製造工程において、乾燥または
焼成後の該成形物にコロイド状シリカ液と界面活ff1
lJもしくは水溶性有機物からなる含浸液を含浸させる
ととKより、900℃焼成のテス)&−スでその圧縮強
度は#景ソ200〜400チに改良されてお知、本発明
が強度面ですぐれた耐火物の製造方法を提供するもので
あることがわかる。
As explained above, in the refractory manufacturing process that involves drying or firing a molded product obtained by molding a refractory material powder or a refractory material powder and a binder, colloids are added to the molded product after drying or firing. silica liquid and surfactant ff1
It is known that when impregnated with an impregnating liquid consisting of lJ or water-soluble organic matter, the compressive strength is improved to 200 to 400 cm when fired at 900°C. It can be seen that the method provides an excellent method for manufacturing refractories.

Claims (1)

【特許請求の範囲】 1、 耐火材料粉末単独または耐火材料粉末と粘結剤を
成形し、得られた成形物を乾燥し、必要に応じて焼成す
ることからなる耐火物の製造法において、乾燥後首たは
焼成後の該成形物にコロイド状シリカ液と界面活性剤ま
たは水溶性有機物とからなる含浸液を含浸させ、しかる
後これを乾燥または焼成することを特徴とする耐火物の
製造法。 2、 前記の含浸液に含まれるコロイド状シリカ液の8
10.乾燥重量対界面活性剤重量または水溶性有機物重
量の比が100:0.15から100:20の範囲にあ
る特許請求の範囲第1項記載の方法。 3、 前記の界面活性剤がシアルギルスルフオサクシネ
ート、高アルコールサルフェート及びポリオキシエチレ
ンアルキルフェニルエーテルから選ばれる特許請求の範
囲第1項記載の方法。 4、 前記の水溶性有機物がメチルアルコール、エチル
アルコール、アセトン及びメチルエチルケトンから選ば
れる特許請求の範囲第1項記載の方法。
[Scope of Claims] 1. A method for producing a refractory, which comprises molding a refractory material powder alone or a refractory material powder and a binder, drying the resulting molded product, and firing if necessary. A method for producing a refractory, which comprises impregnating the molded product after firing or firing with an impregnating liquid consisting of a colloidal silica liquid and a surfactant or a water-soluble organic substance, and then drying or firing the same. . 2. 8 of the colloidal silica liquid contained in the above impregnating liquid.
10. A method according to claim 1, wherein the ratio of dry weight to surfactant weight or water-soluble organic matter weight is in the range of 100:0.15 to 100:20. 3. The method of claim 1, wherein the surfactant is selected from sialygyl sulfosuccinates, high alcohol sulfates, and polyoxyethylene alkylphenyl ethers. 4. The method according to claim 1, wherein the water-soluble organic substance is selected from methyl alcohol, ethyl alcohol, acetone, and methyl ethyl ketone.
JP57108522A 1982-06-25 1982-06-25 Manufacture of refractories impregnated with surfactant or water-soluble organic matter Granted JPS593082A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57108522A JPS593082A (en) 1982-06-25 1982-06-25 Manufacture of refractories impregnated with surfactant or water-soluble organic matter

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57108522A JPS593082A (en) 1982-06-25 1982-06-25 Manufacture of refractories impregnated with surfactant or water-soluble organic matter

Publications (2)

Publication Number Publication Date
JPS593082A true JPS593082A (en) 1984-01-09
JPH0235710B2 JPH0235710B2 (en) 1990-08-13

Family

ID=14486930

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57108522A Granted JPS593082A (en) 1982-06-25 1982-06-25 Manufacture of refractories impregnated with surfactant or water-soluble organic matter

Country Status (1)

Country Link
JP (1) JPS593082A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2015048293A (en) * 2013-09-04 2015-03-16 Jfeスチール株式会社 Shaped refractory and method for producing the same

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5238849A (en) * 1975-09-23 1977-03-25 Nec Corp I/o request processing system
JPS5713517A (en) * 1980-06-27 1982-01-23 Nippon Denso Co Ltd Load operation inspection device

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5238849A (en) * 1975-09-23 1977-03-25 Nec Corp I/o request processing system
JPS5713517A (en) * 1980-06-27 1982-01-23 Nippon Denso Co Ltd Load operation inspection device

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2015048293A (en) * 2013-09-04 2015-03-16 Jfeスチール株式会社 Shaped refractory and method for producing the same

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