JPH06345529A - Production of architectural burnt plate - Google Patents

Production of architectural burnt plate

Info

Publication number
JPH06345529A
JPH06345529A JP5133218A JP13321893A JPH06345529A JP H06345529 A JPH06345529 A JP H06345529A JP 5133218 A JP5133218 A JP 5133218A JP 13321893 A JP13321893 A JP 13321893A JP H06345529 A JPH06345529 A JP H06345529A
Authority
JP
Japan
Prior art keywords
raw material
inorganic powder
molded body
temperature
calcium silicate
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
JP5133218A
Other languages
Japanese (ja)
Inventor
Kei Ito
圭 伊藤
Kazunori Tsutsumi
一徳 堤
Hiroaki Kuniya
宏明 國屋
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.)
Daiken Trade and Industry Co Ltd
Original Assignee
Daiken Trade and Industry 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 Daiken Trade and Industry Co Ltd filed Critical Daiken Trade and Industry Co Ltd
Priority to JP5133218A priority Critical patent/JPH06345529A/en
Publication of JPH06345529A publication Critical patent/JPH06345529A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To provide a production method of an architectural burnt plate with a high productivity, which does not occur cracking at the drying and burning. CONSTITUTION:Siliceous raw material, a calcareous raw material and inorganic powder containing a vitreous component are indispensable constituents and a molding is formed of a mixture obtained with addition of water to these and mixing. An autoclave treatment is carried out so as to produce a calcium silicate hydrate in the obtained molding. Consequently it is burnt at temp. from <=1400 deg.C to >= a softening point of the vitreous component contained in the inorganic powder.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、主として内外装の仕上
げ材に用いる建築用焼成板の製造方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for manufacturing a fired plate for construction, which is mainly used as a finishing material for interiors and exteriors.

【0002】[0002]

【従来の技術と発明が解決しようする課題】従来、建築
用焼成板の製造方法としては、焼成収縮を改善し、生産
性に優れた建築用焼成板を得るため、例えば、セメント
の水和硬化とガラスの融着とを利用したセメント−ガラ
ス系陶磁器製品の製造方法にかかる改良技術(特願平2
−199970号、特願平4−339656号)が提案
されている。
2. Description of the Related Art Conventionally, as a method for producing a fired board for construction, there has been used a method for producing a fired board for construction which has improved firing shrinkage and excellent productivity. Technology related to a method for manufacturing a cement-glass ceramic product using the fusion of glass and glass (Japanese Patent Application No.
-199970 and Japanese Patent Application No. 4-339656) have been proposed.

【0003】しかしながら、前述の先行技術では、成形
後に運搬したり、加工するために一定の強度が必要であ
るので、養生させて水和硬化させる必要がある。このた
め、数日間の養生期間が必要であり、より一層の生産性
の向上が望まれている。また、一連の先行技術では、乾
燥時や焼成時の熱応力によってクラックが発生しやす
く、製造工程における歩留まりが悪くなるという問題点
があり、さらに、未水和部分が焼成後も残存している
と、長期に渡って徐々に再水和し、基材内の膨張によっ
てクラックが発生したり、遊離するアルカリ成分によっ
て白華現象が発生したりするおそれが全くないとはいえ
ない。
However, in the above-mentioned prior art, a certain strength is required for carrying or processing after molding, so that it is necessary to cure and hydrate it. For this reason, a curing period of several days is required, and further improvement in productivity is desired. Further, in a series of prior art, there is a problem that cracks easily occur due to thermal stress at the time of drying or firing, and the yield in the manufacturing process deteriorates. Furthermore, the unhydrated portion remains after firing. Therefore, it cannot be said that there is no possibility that it will gradually rehydrate over a long period of time, and that cracks will occur due to expansion in the base material and that the white flower phenomenon will occur due to the released alkaline component.

【0004】本発明は、前記問題点に鑑み、生産性が高
く、乾燥,焼成時にクラックが生じない建築用焼成板の
製造方法を提供することを目的とする。
In view of the above problems, it is an object of the present invention to provide a method for manufacturing a fired building plate, which has high productivity and does not cause cracks during drying and firing.

【0005】[0005]

【課題を解決するための手段】本発明者らは、前記目的
を達成するため、鋭意研究の結果、成形体を成形した
後、焼成前に、珪酸カルシウム水和物を生成するように
オートクレーブ処理を施すと、養生期間が短縮し、乾
燥,焼成時にクラック等が生じないことを知見し、この
知見に基づいて本発明を完成した。
[Means for Solving the Problems] In order to achieve the above-mentioned object, the inventors of the present invention have conducted extensive studies and, as a result, have carried out an autoclave treatment to form a calcium silicate hydrate after forming a molded body and before firing. It was found that the curing time was shortened and cracks did not occur during drying and firing, and the present invention was completed based on this finding.

【0006】すなわち、本発明の要旨は、珪酸質原料
と、石灰質原料と、ガラス質成分を含む無機質粉体とを
必須成分とし、これらに水を添加,混合して得た混合物
で成形体を成形し、得られた成形体に珪酸カルシウム水
和物を生成するようにオートクレーブ処理を施した後、
無機質粉体に含まれるガラス質成分の軟化点以上で14
00℃以下の温度で焼成することを特徴とする建築用焼
成板の製造方法にある。また、前述の製造方法において
は、オートクレーブ処理後、焼成前に、成形体の表面に
釉薬原料を塗布したり、表面加工を施したり、あるい
は、表面加工を施して釉薬原料を塗布してもよい。
That is, the gist of the present invention is that a siliceous raw material, a calcareous raw material, and an inorganic powder containing a vitreous component are essential components, and water is added to and mixed with these to form a molded body. After molding and subjecting the resulting molded body to an autoclave treatment to produce calcium silicate hydrate,
14 above the softening point of the glassy component contained in the inorganic powder
A method for producing a fired plate for construction is characterized by firing at a temperature of 00 ° C. or lower. Further, in the above-described manufacturing method, after the autoclave treatment and before firing, the surface of the molded body may be coated with a glaze raw material, may be subjected to a surface treatment, or may be subjected to a surface treatment to apply the glaze raw material. .

【0007】珪酸質原料は、後述する石灰質原料との水
和反応によって硬化することにより、焼成前の成形体の
強度を発現するとともに、焼成時に起こる収縮を低減す
るために添加されるものであり、例えば、珪藻土,硅石
粉,硅砂,酸性白土,ベンナイト等が挙げられ、混合物
の固形成分全体の10〜50重量%が添加される。10
重量%未満であると、珪酸カルシウムの生成反応に必要
な二酸化珪素成分が不足するからであり、50重量%を
越えると、相対的に酸化カルシウム成分やガラス質成分
が不足するからである。
The siliceous raw material is added in order to develop the strength of the green body before firing by hardening by the hydration reaction with the calcareous raw material described later and to reduce the shrinkage that occurs during firing. Examples thereof include diatomaceous earth, silica powder, silica sand, acid clay, and bentonite, and 10 to 50% by weight of the total solid components of the mixture is added. 10
This is because if it is less than wt%, the silicon dioxide component necessary for the calcium silicate formation reaction will be insufficient, and if it exceeds 50 wt%, the calcium oxide component and the vitreous component will be relatively insufficient.

【0008】石灰質原料としては、例えば、セメント,
消石灰,生石灰等が挙げられ、混合物の固形成分全体の
10〜30重量%が添加される。10重量%未満である
と、珪酸カルシウムの生成反応に必要な酸化カルシウム
成分が不足するからであり、30重量%を越えると、相
対的に二酸化珪素成分やガラス質成分が不足するからで
ある。
Examples of calcareous raw materials include cement,
Examples include slaked lime and quick lime, and 10 to 30% by weight of the total solid components of the mixture is added. This is because if it is less than 10% by weight, the calcium oxide component necessary for the reaction of forming calcium silicate is insufficient, and if it exceeds 30% by weight, the silicon dioxide component and the vitreous component are relatively insufficient.

【0009】なお、後述する珪酸カルシウム水和物を効
率的に生成するためには珪酸質原料と石灰質原料との配
合比をCaO/SiO2のモル比で0.5〜1.5、好
ましくは0.7〜1.1とする必要がある。そして、両者
の総添加量は混合物の固形成分全体の 20〜70重量
%であることが好ましい。20重量%未満であると、成
形体の強度が不足するとともに、焼成収縮が増加するか
らであり、70重量%を越えると、ガラス質成分の不足
によって焼成後の最終強度が不足するからである。
In order to efficiently produce the calcium silicate hydrate described below, the mixing ratio of the siliceous raw material and the calcareous raw material is 0.5 to 1.5, preferably CaO / SiO 2 molar ratio. It is necessary to set it to 0.7 to 1.1. The total addition amount of both is preferably 20 to 70% by weight based on the total solid components of the mixture. This is because if it is less than 20% by weight, the strength of the molded article becomes insufficient and firing shrinkage increases, and if it exceeds 70% by weight, the final strength after firing becomes insufficient due to the lack of vitreous components. .

【0010】ガラス質成分を含む無機質粉体は、焼成に
よってガラス質成分の溶融,融着によって焼成後の強度
を得るために添加されるものであり、例えば、シラス,
フライアッシュ,抗火石,ガラス粉,スラグ等が挙げら
れ、混合物の固形成分全体の20〜80重量%が添加さ
れる。20重量%未満であると、焼成後の強度が低いか
らであり、80重量%を越えると、相対的に珪酸質原料
および石灰質原料の添加量が減少し、焼成前の強度が低
くなるからである。
The inorganic powder containing the vitreous component is added to obtain the strength after firing by melting and fusing the vitreous component by firing.
Fly ash, anti-fire stone, glass powder, slag and the like are included, and 20 to 80% by weight of the total solid components of the mixture is added. This is because if it is less than 20% by weight, the strength after firing is low, and if it exceeds 80% by weight, the addition amount of siliceous raw material and calcareous raw material is relatively reduced, and the strength before firing becomes low. is there.

【0011】水の添加量は特に限定しないが、後述する
混合作業や成形作業の必要に応じて適宜添加してよい。
なお、押し出し成形する場合には、押し出し成形直後の
形状を維持するため、メチルセルロース,カルボキシメ
チルセルロース,ポバール等の増粘剤を添加してもよ
い。また、抄造成形する場合には、抄造する際の濾水性
を向上させるため、パルプ,ロックウール等の繊維、お
よび/または、アクリルアミド等の凝集剤を添加しても
よい。
The amount of water to be added is not particularly limited, but may be appropriately added depending on the needs of the mixing operation and molding operation described later.
In the case of extrusion molding, a thickening agent such as methyl cellulose, carboxymethyl cellulose or poval may be added to maintain the shape immediately after extrusion molding. Further, in the case of papermaking and molding, fibers such as pulp and rockwool and / or a flocculant such as acrylamide may be added to improve drainage during papermaking.

【0012】混合方法は特に限定するものでなく、既存
の混合方法から任意に選択でき、例えば、ニーダー,ミ
キサー等で適宜混合して混合物を得ればよい。
The mixing method is not particularly limited and can be arbitrarily selected from existing mixing methods. For example, a mixture may be obtained by appropriately mixing with a kneader, a mixer or the like.

【0013】成形方法は既存の成形方法から任意に選択
でき、例えば、押し出し成形,抄造成形,プレス成形等
によって成形してよい。
The molding method can be arbitrarily selected from existing molding methods, and may be, for example, extrusion molding, papermaking molding, press molding or the like.

【0014】オートクレーブ処理は、前記成形体内に安
定した珪酸カルシウム水和物を短時間で生成し、遊離し
たアルカリ成分をなくすことにより、養生期間を短縮し
て生産性を向上するとともに、焼成後の使用時における
再水和を防止し、成形体内の膨張でクラックが生じた
り、遊離したアルカリ成分によって白華現象が生じたり
するのを防止するために行われる。そして、オートクレ
ーブ処理は、温度120〜250℃,圧力2〜39気圧
で1〜20時間、ただし、時間効率から考えて温度15
0〜200℃,圧力4.5〜16気圧で3〜10時間と
するのが好適である。温度が120℃未満であると、ト
ベルモライトを生成する反応が不十分となるからであ
り、温度が250℃を越えると、トベルモライトの結晶
がゾノトライトに変わり、却って強度が低下するからで
ある。また、処理時間が1時間未満であると、珪酸カル
シウム水和物を生成する反応の進行が不十分であり、2
0時間を越えると、それ以上反応せず、生産性が低下す
るからである。
In the autoclave treatment, stable calcium silicate hydrate is formed in the molded body in a short time, and the liberated alkaline component is eliminated, thereby shortening the curing period and improving the productivity, and at the same time, after firing. It is carried out in order to prevent rehydration at the time of use and to prevent cracks due to expansion in the molded body and the white flower phenomenon due to the released alkaline component. The autoclave treatment is carried out at a temperature of 120 to 250 ° C. and a pressure of 2 to 39 atm for 1 to 20 hours, but at a temperature of 15 at the time efficiency.
It is preferable that the temperature is 0 to 200 ° C. and the pressure is 4.5 to 16 atm for 3 to 10 hours. This is because if the temperature is lower than 120 ° C, the reaction to form tobermorite will be insufficient, and if the temperature exceeds 250 ° C, the crystals of tobermorite will change to zonotolite and the strength will rather decrease. is there. Further, if the treatment time is less than 1 hour, the progress of the reaction for forming calcium silicate hydrate is insufficient, and 2
This is because if it exceeds 0 hours, no further reaction occurs and the productivity decreases.

【0015】このようにオートクレーブ処理で珪酸カル
シウム水和物を生成するのは、この水和物の熱劣化が少
ないからである。すなわち、一般に、室温養生による水
和反応後に400℃まで加熱すると、強度が45%程度
まで劣化し、800℃まで加熱すると、強度が20%程
度まで劣化するのに対し、オートクレーブ処理による水
和反応後に400℃まで加熱すると、強度が90%程度
まで劣化し、800℃まで加熱すると、強度が50%程
度まで劣化するにすぎず、強度劣化の程度が改善される
からである。
The reason why calcium silicate hydrate is produced by the autoclave treatment is that the hydrate is less thermally deteriorated. That is, generally, when heated to 400 ° C. after the hydration reaction by room temperature curing, the strength deteriorates to about 45%, and when heated to 800 ° C., the strength deteriorates to about 20%, whereas the hydration reaction by the autoclave treatment deteriorates. This is because if it is heated to 400 ° C. later, the strength deteriorates to about 90%, and if it is heated to 800 ° C., the strength only deteriorates to about 50% and the degree of strength deterioration is improved.

【0016】なお、オートクレーブ処理後も成形体内に
残留する水分を原因とする焼成時のクラックの発生を防
止するため、オートクレーブ処理後、焼成前に成形体を
乾燥することが好ましく、特に、含水率を3重量%以下
まで乾燥しておくことが望ましい。
It is preferable to dry the molded product after the autoclave treatment and before the firing, in order to prevent the occurrence of cracks during the baking due to the water remaining in the molded body after the autoclave treatment, and in particular, the water content. Is preferably dried to 3% by weight or less.

【0017】焼成作業は無機質粉体に含まれるガラス質
成分を融着させて強度を発現するために行われるもので
あり、焼成温度は、無機質粉体に含まれるガラス質成分
の軟化点以上、望ましくは粘度が105poise(「リ
リー点」という)となる粘性温度の±50℃以上で、温度
1400℃以下の範囲内であればよい。焼成温度を14
00℃以下とするのは、1400℃を越えると、ガラス
質成分等が焼成によって変形するからである。
The firing operation is performed in order to fuse the glassy components contained in the inorganic powder to develop strength, and the firing temperature is higher than the softening point of the glassy component contained in the inorganic powder, Desirably, the viscosity is within a range of ± 50 ° C. or higher and 1400 ° C. or lower of the viscosity temperature at which the viscosity becomes 10 5 poise (referred to as “Lily point”). Firing temperature 14
The reason why the temperature is set to 00 ° C. or lower is that when the temperature exceeds 1400 ° C., the glassy components and the like are deformed by firing.

【0018】なお、焼成前に釉薬原料の塗布、表面加
工、または、表面加工後に釉薬原料を塗布してもよい。
釉薬原料は特に限定するものではなく、既存の陶磁器用
釉薬から任意に選択できる。また、表面加工も特に限定
するものでなく、例えば、ロールエンボス加工,ルータ
ー加工,サンドブラスト加工などの既存の方法から任意
に選択してもよい。
The glaze raw material may be applied or surface-treated before firing, or the glaze raw material may be applied after the surface-treatment.
The glaze raw material is not particularly limited, and can be arbitrarily selected from existing glazes for ceramics. Further, the surface processing is not particularly limited, and may be arbitrarily selected from existing methods such as roll embossing, router processing, and sandblasting.

【0019】[0019]

【作用】したがって、本発明によれば、焼成前のオート
クレーブ処理によって成形体内に珪酸カルシウム水和物
が生成することになる。
Therefore, according to the present invention, calcium silicate hydrate is formed in the molded body by the autoclave treatment before firing.

【0020】[0020]

【実施例】次に、本発明にかかる実施例を説明する。 (実施例1)珪酸質原料として酸性白土を10重量%、
硅砂5号を18重量%、石灰質原料として普通ポルトラ
ンドセメントを30重量%、ガラス質成分を含む無機質
粉体として抗火石を40重量%、増粘剤としてメチルセ
ルロースを2重量%、これら粉体の総重量100に対し
て20の割合で水を添加し、ニーダーで混合して混合物
を得た後、真空押し出し機で巾300mm、高さ20m
m、肉厚8mm、長さ1000mmの断面長方形の中空
成形体を得た。そして、この中空成形体に温度180
℃、圧力10気圧で3時間のオートクレーブ処理を施
し、ついで、温度120℃で2時間乾燥させた後、通常
の陶磁器用釉薬をスプレーで約600g/m2の割合で塗
布し、ローラーハースキルンで120分間、そのうち、
最高温度1130℃で15分間焼成し、得られた焼成体
をサンプルとした。
EXAMPLES Next, examples according to the present invention will be described. (Example 1) 10% by weight of acid clay as a siliceous raw material,
18% by weight of silica sand, 30% by weight of ordinary Portland cement as a calcareous raw material, 40% by weight of anti-fire stone as an inorganic powder containing a glassy component, 2% by weight of methylcellulose as a thickening agent, and a total of these powders. Water was added at a ratio of 20 to 100 by weight and mixed with a kneader to obtain a mixture, which was then 300 mm wide and 20 m high by a vacuum extruder.
A hollow molded body having a rectangular cross-section with m, a wall thickness of 8 mm and a length of 1000 mm was obtained. Then, the hollow molded body is heated to a temperature of 180.
After autoclaving for 3 hours at 10 ° C and a pressure of 10 atm, and then drying for 2 hours at 120 ° C, apply a normal glaze for ceramics by spraying at a rate of about 600 g / m 2 , and use a roller hearth kiln. 120 minutes, of which
The sample was baked at a maximum temperature of 1130 ° C. for 15 minutes, and the obtained baked product was used as a sample.

【0021】このサンプルの曲げ強度は平均で180k
gf/cm2であり、目視でサンプルの表面を観察した
ところ、クラックの発生は見受けられなかった。
The bending strength of this sample is 180 k on average.
It was gf / cm 2 , and when the surface of the sample was visually observed, no crack was found.

【0022】(比較例1)珪酸質原料として硅砂5号を
18重量%、石灰質原料として普通ポルトランドセメン
トを40重量%、ガラス質成分を含む無機質粉体として
抗火石を40重量%、これらに増粘剤としてメチルセル
ロースを2重量%を添加し、さらに、オートクレーブ処
理の代わりに、密封した室内に成形体を2日間放置して
養生した点を除き、他は前述の実施例1と同様に処理し
て得られた焼成体をサンプルとした。
(Comparative Example 1) 18% by weight of silica sand No. 5 as a siliceous raw material, 40% by weight of ordinary Portland cement as a calcareous raw material, and 40% by weight of anti-firestone as an inorganic powder containing a vitreous component. 2% by weight of methyl cellulose was added as a viscous agent, and the same treatment as in Example 1 was carried out except that the molded body was allowed to cure for 2 days in a sealed room instead of being autoclaved. The fired body thus obtained was used as a sample.

【0023】乾燥によってサンプル全体の約10%の製
品にクラックが発生し、クラックを生じたサンプルを除
いて行った焼成によって残るサンプル全体の約20%の
製品にクラックが発生していた。また、クラックが生じ
ていない正常なサンプルの曲げ強度は平均で170kg
f/cm2であった。
About 10% of the whole sample was cracked by the drying, and about 20% of the whole sample remained after the firing except the cracked sample was cracked. Also, the bending strength of a normal sample without cracks is 170 kg on average.
It was f / cm 2 .

【0024】(実施例2)珪酸質原料としてベンナイト
を20重量%、硅砂5号を10重量%、石灰質原料とし
て消石灰を30重量%、ガラス質成分を含む無機質粉体
としてシラス40重量%をミキサーで混合して混合粉体
を得た。一方、古紙パルプとロックウールとを1対2の
重量比で水に混合して解織した後、前記混合粉体と繊維
とを固形分比で10対1となるように混合し、さらに、
凝集剤としてポリアクリルアミドを固形分全体の0.5
重量%添加し、ついで、水を適宜投入して濃度10%の
スラリーを得た。そして、このスラリーを丸網抄造機に
導入して厚さ6mmの湿潤マットを抄造した後、この湿
潤マットを巾300mm、長さ900mmに切断して成
形体を得、この成形体に温度180℃、圧力10気圧で
3時間のオートクレーブ処理を施し、ついで、温度12
0℃で2時間乾燥させた後、その表面に陶磁器用釉薬を
約600g/m2の割合でスプレーで塗布し、ローラーハ
ースキルンによって90分間、そのうち、最高温度11
30℃で15分間焼成し、得られた焼成体をサンプルと
した。
(Example 2) As a siliceous raw material, 20% by weight of bentonite, 10% by weight of silica sand No. 5, 30% by weight of slaked lime as a calcareous raw material, and 40% by weight of shirasu as an inorganic powder containing a vitreous component were mixed. To obtain a mixed powder. On the other hand, waste paper pulp and rock wool are mixed in water at a weight ratio of 1: 2 and woven, and then the mixed powder and fibers are mixed at a solid content ratio of 10: 1.
Polyacrylamide as a coagulant is added to 0.5 of the total solid content.
Wt% was added, and then water was appropriately added to obtain a slurry having a concentration of 10%. Then, this slurry was introduced into a gauze machine to make a wet mat having a thickness of 6 mm, and the wet mat was cut into a width of 300 mm and a length of 900 mm to obtain a molded body, and the molded body had a temperature of 180 ° C. Autoclave for 3 hours at a pressure of 10 atm and then a temperature of 12
After drying at 0 ° C for 2 hours, a glaze for ceramics was sprayed on the surface at a rate of about 600 g / m 2 , and 90 minutes by a roller hearth kiln, the maximum temperature of which was 11
The sample was baked at 30 ° C. for 15 minutes, and the obtained baked product was used as a sample.

【0025】このサンプルの曲げ強度は平均で105k
gf/cm2であり、目視でサンプルの表面を観察した
ところ、クラックの発生は見受けられなかった。
The bending strength of this sample is 105 k on average.
It was gf / cm 2 , and when the surface of the sample was visually observed, no crack was found.

【0026】(比較例2)珪酸質原料として硅砂5号を
10重量%、石灰質原料として普通ポルトランドセメン
トを50重量%、ガラス質成分を含む無機質粉体として
シラス40重量%を添加し、さらに、オートクレーブ処
理の代わりに、密封した室内に成形体を2日間放置して
養生した点を除き、他は前述の実施例2と同様に処理し
て得られた焼成体をサンプルとした。
(Comparative Example 2) Silica No. 5 was added as a siliceous raw material in an amount of 10% by weight, ordinary Portland cement was added as a calcareous raw material in an amount of 50% by weight, and Shirasu as an inorganic powder containing a vitreous component in an amount of 40% by weight. Instead of the autoclave treatment, a fired body obtained by the same treatment as in Example 2 was used as a sample, except that the molded body was left for 2 days to cure in a sealed chamber.

【0027】乾燥によってサンプル全体の約15%の製
品にクラックが発生し、クラックを生じたサンプルを除
いて行った焼成によって残るサンプル全体の約15%の
製品にクラックが発生していた。また、クラックが生じ
ていない正常なサンプルの曲げ強度は平均で100kg
f/cm2であった。
Approximately 15% of the products were cracked by the drying, and about 15% of the products remaining after the firing except the cracked products were cracked. In addition, the bending strength of a normal sample without cracks is 100 kg on average.
It was f / cm 2 .

【0028】[0028]

【発明の効果】以上の説明から明らかなように、本発明
にかかる建築用焼成板の製造方法によれば、オートクレ
ーブ処理により、成形体の大部分が短時間で安定した珪
酸カルシウム水和物(主としてトベルモライト)となる
ので、従来例のように成形後に長時間の養生を行う必要
がなくなり、成形してから短時間で焼成でき、生産性が
向上する。しかも、オートクレーブ処理により、成形体
の大部分は主としてトベルモライトから成る安定した珪
酸カルシウム水和物となり、乾燥,焼成時に熱応力が生
じても、クラックが発生せず、製造工程における歩留ま
りが向上するという効果がある。
As is apparent from the above description, according to the method for producing a fired plate for construction according to the present invention, most of the molded body is stable in a short time by the autoclave treatment (calcium silicate hydrate ( Since it mainly becomes tobermorite, it is not necessary to carry out curing for a long time after molding as in the conventional example, and it can be fired in a short time after molding, and the productivity is improved. Moreover, by autoclaving, most of the molded body becomes a stable calcium silicate hydrate mainly composed of tobermorite, and even if thermal stress occurs during drying and firing, cracks do not occur and the yield in the manufacturing process is improved. There is an effect of doing.

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】 珪酸質原料と、石灰質原料と、ガラス質
成分を含む無機質粉体とを必須成分とし、これらに水を
添加,混合して得た混合物で成形体を成形し、得られた
成形体に珪酸カルシウム水和物を生成するようにオート
クレーブ処理を施した後、無機質粉体に含まれるガラス
質成分の軟化点以上で1400℃以下の温度で焼成する
ことを特徴とする建築用焼成板の製造方法。
1. A siliceous raw material, a calcareous raw material, and an inorganic powder containing a glassy component are essential components, and water is added to and mixed with them to form a molded body, which is obtained. Calcination for construction characterized by calcining at a temperature not lower than 1400 ° C above the softening point of the glassy component contained in the inorganic powder after autoclaving the formed body to produce calcium silicate hydrate Method of manufacturing a plate.
【請求項2】 珪酸質原料と、石灰質原料と、ガラス質
成分を含む無機質粉体とを必須成分とし、これらに水を
添加,混合して得た混合物で成形体を成形し、得られた
成形体に珪酸カルシウム水和物を生成するようにオート
クレーブ処理を施した後、その表面に釉薬原料を塗布
し、無機質粉体に含まれるガラス質成分の軟化点以上で
1400℃以下の温度で焼成することを特徴とする建築
用焼成板の製造方法。
2. A siliceous raw material, a calcareous raw material, and an inorganic powder containing a vitreous component as essential components, and water is added to and mixed with them to form a molded body, which is obtained. After autoclaving the formed body to produce calcium silicate hydrate, apply glaze raw material on the surface and fire at a temperature of 1400 ° C or lower above the softening point of the glassy component contained in the inorganic powder. A method of manufacturing a fired plate for construction, comprising:
【請求項3】 珪酸質原料と、石灰質原料と、ガラス質
成分を含む無機質粉体とを必須成分とし、これらに水を
添加,混合して得た混合物で成形体を成形し、得られた
成形体に珪酸カルシウム水和物を生成するようにオート
クレーブ処理を施した後、その表面に表面加工を施し、
無機質粉体に含まれるガラス質成分の軟化点以上で14
00℃以下の温度で焼成することを特徴とする建築用焼
成板の製造方法。
3. A molded product was obtained by molding a mixture obtained by adding and mixing water to a siliceous raw material, a calcareous raw material, and an inorganic powder containing a glassy component as essential components. After subjecting the molded body to an autoclave treatment to generate calcium silicate hydrate, the surface is subjected to a surface treatment,
14 above the softening point of the glassy component contained in the inorganic powder
A method for manufacturing a fired board for construction, which comprises firing at a temperature of 00 ° C or lower.
【請求項4】 珪酸質原料と、石灰質原料と、ガラス質
成分を含む無機質粉体とを必須成分とし、これらに水を
添加,混合して得た混合物で成形体を成形し、得られた
成形体に珪酸カルシウム水和物を生成するようにオート
クレーブ処理を施した後、その表面に表面加工を施して
釉薬原料を塗布し、無機質粉体に含まれるガラス質成分
の軟化点以上で1400℃以下の温度で焼成することを
特徴とする建築用焼成板の製造方法。
4. A molded body is obtained by molding a mixture obtained by adding and mixing water to these as essential components, a siliceous raw material, a calcareous raw material, and an inorganic powder containing a glassy component. After subjecting the molded body to an autoclave treatment to generate calcium silicate hydrate, surface treatment is applied to the surface and glaze raw material is applied, and the temperature is 1400 ° C or higher at the softening point of the vitreous component contained in the inorganic powder. A method for producing a fired plate for construction, which comprises firing at the following temperature.
JP5133218A 1993-06-03 1993-06-03 Production of architectural burnt plate Pending JPH06345529A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5133218A JPH06345529A (en) 1993-06-03 1993-06-03 Production of architectural burnt plate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5133218A JPH06345529A (en) 1993-06-03 1993-06-03 Production of architectural burnt plate

Publications (1)

Publication Number Publication Date
JPH06345529A true JPH06345529A (en) 1994-12-20

Family

ID=15099498

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5133218A Pending JPH06345529A (en) 1993-06-03 1993-06-03 Production of architectural burnt plate

Country Status (1)

Country Link
JP (1) JPH06345529A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005194151A (en) * 2004-01-09 2005-07-21 Nichiha Corp Inorganic board
JP2005194142A (en) * 2004-01-08 2005-07-21 Nichiha Corp Method for producing inorganic board

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5146305A (en) * 1974-10-18 1976-04-20 Kogyo Gijutsuin Keiryotaikazaino seizoho
JPS59167203A (en) * 1983-03-15 1984-09-20 太平洋セメント株式会社 Method of working surface of building board
JPS61242971A (en) * 1985-04-22 1986-10-29 旭化成株式会社 Manufacture of crystalline calcium silicate hydrate extrusion formed body
JPS61291478A (en) * 1985-06-17 1986-12-22 三菱セメント建材株式会社 Surface treatment for construction material
JPH03223187A (en) * 1990-01-30 1991-10-02 Sumitomo Metal Mining Co Ltd Production of glazed light-weight calcium silicate material

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5146305A (en) * 1974-10-18 1976-04-20 Kogyo Gijutsuin Keiryotaikazaino seizoho
JPS59167203A (en) * 1983-03-15 1984-09-20 太平洋セメント株式会社 Method of working surface of building board
JPS61242971A (en) * 1985-04-22 1986-10-29 旭化成株式会社 Manufacture of crystalline calcium silicate hydrate extrusion formed body
JPS61291478A (en) * 1985-06-17 1986-12-22 三菱セメント建材株式会社 Surface treatment for construction material
JPH03223187A (en) * 1990-01-30 1991-10-02 Sumitomo Metal Mining Co Ltd Production of glazed light-weight calcium silicate material

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005194142A (en) * 2004-01-08 2005-07-21 Nichiha Corp Method for producing inorganic board
JP2005194151A (en) * 2004-01-09 2005-07-21 Nichiha Corp Inorganic board

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