JPH0411499B2 - - Google Patents

Info

Publication number
JPH0411499B2
JPH0411499B2 JP12953284A JP12953284A JPH0411499B2 JP H0411499 B2 JPH0411499 B2 JP H0411499B2 JP 12953284 A JP12953284 A JP 12953284A JP 12953284 A JP12953284 A JP 12953284A JP H0411499 B2 JPH0411499 B2 JP H0411499B2
Authority
JP
Japan
Prior art keywords
fibers
cement
product
temperature
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
JP12953284A
Other languages
Japanese (ja)
Other versions
JPS6117464A (en
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 filed Critical
Priority to JP12953284A priority Critical patent/JPS6117464A/en
Publication of JPS6117464A publication Critical patent/JPS6117464A/en
Publication of JPH0411499B2 publication Critical patent/JPH0411499B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Curing Cements, Concrete, And Artificial Stone (AREA)
  • Aftertreatments Of Artificial And Natural Stones (AREA)
  • Press-Shaping Or Shaping Using Conveyers (AREA)

Description

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

『発明の目的』 〔産業上の利用分野〕 本発明は、セメント、繊維、水を主成分とする
原料の混合物を押し出し成形して得られた成形体
の表面に、釉薬を塗布して焼成することで釉薬層
を形成するようにした施釉セメント製品の製造方
法に関するものである。 〔従来の技術〕 通常、押出成形により施釉セメント製品を製造
する場合は、普通ポルトランドセメント、早強セ
メント、高炉スラグセメント等のセメント(以
下、単にセメントと称する)、繊維、水を主成分
とする混合物に必要に応じて骨材、添加材を加え
て混合し、該混合物を押出成形した成形体の表面
に施釉をし、然る後に焼成、水和硬化させて製品
としている。この場合にあつて、繊維は押出性、
保形性を良くするためのものであり、石綿繊維を
用いるのが一般的である。また骨材は、珪砂、硬
質砂岩、川砂、陶磁器タイルや衛生陶器の破砕物
等が用いられており、添加材は、可塑材、減水
材、膨張材等が用いられている。 〔本発明が解決しようとする問題点〕 従来の上記施釉セメント製品の押出成形による
製造方法にあつては、次のような欠点があつた。
すなわち、 (1) 主成分として使用する繊維が石綿繊維である
がために、製品の釉薬層の中にピンホールが残
存することがあり、美観を損なうと共に耐凍害
性に欠け、製品価値を著しく低減させるという
欠点があつた。 (2) また焼成時にあつて、石綿繊維中に含まれる
Mgが小量固溶することによつてα′−C2Sが生
成され、その後の水和硬化における機械的強度
の発現性が遅くなるという欠点があつた。 本発明者らがこれらの欠点の原因を探求したと
ころ、次の通りであつた。すなわち、上記(1)の欠
点は、石綿繊維として用いられるクリソタイル石
綿(3MgO・2SiO2・2H2O)が、昇温時にあつて
600℃前後から次第に脱水を開始し、崩壊し始め
る。ところが、通常用いられる釉薬も600℃前後
から軟化を始め、700〜900℃程度で溶融する。こ
の釉薬の軟化温度と石綿繊維の脱水温度とがほぼ
一致しているため、脱水により被焼成体(押出成
形体)の表面に蒸発した水分が、軟化して粘度の
高い連続層となつた軟化状態の釉薬層内に封入さ
れるようになる。しかも、釉薬はその後の高温焼
成で完全に溶融しても水のように粘度が低下する
ものではなく、一旦軟化状態の釉薬層内に封入さ
れた水分は、除去されないで残つたままとなる。
それで、結果としてピンホールが発生し、美観が
損なわれると共に耐凍害性の点でも劣るものであ
つた。 また上記(2)の欠点は、施釉セメント製品の本来
有する性質に基づくものである。一般的にこの種
施釉セメント製品にあつては、セメント押出成形
体を施釉、焼成すると、セメント水和物が脱水さ
れてC2SやCSが生成される。このため、焼成体は
一旦機械的強度が低下するが、その後の水和硬化
によつて強度を回復するという性質を有してい
る。ところが、上記C2SやCSは強度発現性が遅
く、強度回復に時間がかかるという性質を有して
いる。このような傾向は、C2Sの種々の変態によ
り差があり、とりわけ、焼成過程における石綿繊
維中のMgが少量固溶することによつて生成され
るα′−C2Sには著しい傾向があつた。 このような欠点は、押出成形で施釉セメント製
品を製造する場合に、石綿繊維を他のセメント、
水と共に主成分としている関係上避けることがで
きないものであつた。 それに最近では、様々な化学製品から析出され
る物質が公害問題となることがクローズアツプさ
れている。この石綿繊維を使用する押出成形によ
る施釉セメント製品の場合も、石綿繊維が発ガン
性物質として、またケイ肺等を生じる物質として
問題となつており、その使用は好ましいものでは
なかつた。 また従来にあつては、サクシヨン成形で施釉セ
メント製品を製造する場合も、押出成形同様に石
綿繊維を使用しており、上述の欠点があつた。 『発明の構成』 〔問題点を解決するための手段〕 本発明は従来の上記欠点に鑑みてこれを解決し
たものであつて、セメント、繊維、水を主成分と
する原料の混合物を押し出し成形し、得られた成
形体の表面に、釉薬を塗布して高温焼成し、その
後水和硬化させることで機械的強度に優れた施釉
セメント製品を製造する場合にあつて、前記繊維
は、ビニロン繊維、アクリル繊維等の有機繊維や
炭素繊維若しくはパルプ繊維等であつて、その焼
失温度が通常の釉薬の溶融温度よりも低い500℃
以下であり、前記成形体を一旦繊維焼失温度で加
熱するか若しくは釉薬焼成時にあつて該繊維焼失
温度まで加熱することで前記繊維を焼失させ、然
る後に650〜900℃の温度で焼成し、該焼成体を水
和硬化させるようにした施釉セメント製品の製造
方法を提供せんとするものである。これにより、
釉薬層にピンホールの発生がなく、美観及び耐凍
害性に優れ、また機械的強度の早期発現性に優れ
た製品の実現を可能としている。 本発明方法は、上述の如く、セメント、繊維、
水を主成分とするものである。而して、セメント
は、普通ポルトランドセメント、アルミナセメン
ト、高炉スラグセメント、混合セメント、早強セ
メントなど通常使用されているセメント(以下、
単にセメントという)から任意に選択することが
可能である。 また繊維は、ビニロン繊維、アクリル繊維等の
有機繊維や炭素繊維、パルブ繊維等のように500
℃以下の温度で焼失するものであればよい。 上述の主成分の他に用いられる材料は、増粘
剤、骨材と、それに減水剤、硬化促進剤、硬化遅
延剤、着色剤等の添加材がある。増粘剤として
は、メチルセルロース、エチルセルロース、カル
ボキシメチルセルロース、ポリエチレンオキシ
ド、ポリビニルアルコールなどが用いられる。特
に好適なのは、メチルセルロースである。また骨
材は、砂、シエルベン、シヤモツト等の通常セメ
ント用骨材として用いられるもので充分である。
減水剤、硬化促進剤、硬化遅延剤、着色剤等の添
加材は、必要に応じて用いられるものである。 本発明方法にあつては、上述の各材料を慣用の
ミキサーに投入して混合する。そして、必要に応
じて該混合物を所定の混練機で混練する。次に、
混練した若しくは混練しない上記混合物を、押出
成形機で所定形状に押出成形する。然る後は、該
押出成形体を気中、水中浸漬等の方法で数時間〜
数日間の予備的水和硬化を行う。そして、予備的
水和硬化後の押出成形体の所望面にガラス粉やフ
リツトを主成分とする通常の釉薬原料をスプレー
掛け、幕掛け、浸漬法などにより施釉する。 次に、施釉された押出成形体を、繊維焼失温度
まで加熱して成形体中に含まれる前述の繊維を焼
失させる。この加熱は、後で行われる焼成とは別
に行つてもよく、また同時であつてもよい。この
繊維焼失温度での加熱は、釉薬の溶融温度以下の
ものであり、繊維が焼失するときの水分は釉薬中
へ溶け込むことはない。つまり、ピンホールの発
生原因となるものではない。 然る後は、押出成形体を650〜900℃の温度で焼
成する。本発明にあつては、従来のように石綿繊
維を使用していないので、焼成によりα′−C2Sが
生成されるということはない。従つて、後で行わ
れる本格的水和硬化時の強度発現性がα′−C2Sに
よつて遅くなるということがなく、早期強度の回
復が得られるものである。 焼成後は、該焼成体を冷却させ、水中浸漬、蒸
気養生、オートクレープ養生等の養生により本格
的水和硬化を行う。なお、上記繊維が焼失した部
分はボアとなるが、その後に行われる本格的水和
硬化時のセメント水和物がこのボアを埋めるので
問題ではない。然しながら、繊維の径が大きい場
合にはセメント水和物でも上記ボアを埋めること
ができないときがあるので、使用する繊維の径は
100μm以下であることが望ましい。 本格的水和硬化が済んだ後は、これを取り出
し、乾燥させればよい。これにより、釉薬層にピ
ンホールの発生がなく、また強度の早期発現性に
優れた施釉セメント製品を得ることができるもの
である。 尚、機械的強度を更に向上させるために、スチ
ールフアイバーやステンレスフアイバーのような
金属繊維やセラミツク繊維等の耐熱繊維を原料混
合時に添加して使用してもよい。この耐熱繊維
は、釉薬の焼成温度でも溶融軟化するなどのこと
はなく、ピンホール等の発生原因となるものでは
ない。更には、押出成形時に金属線材、金属線で
枠組した材料若しくは金属メツシユ等の金属補強
材を埋設するようにしてもよい。この金属補強材
と上記耐熱繊維とを併用すれば、非常に優れた機
械的強度が得られるものである。 次に、本発明方法で製造した施釉セメント製品
と従来方法で製造した施釉セメント製品とを比較
した具体的な実施例について説明する。 〔実施例〕 比較品の製造は、本発明及び従来の双方共に、
表−1に示す原材料を千代田技研工業(株)製の混合
機・OM−30により混合し、更にこれを本田鉄工
(株)製の混練機・PAD−3により混練した。そし
て、該混練後の混合物を本田鉄工(株)製の押出成形
機・DE−100により成形圧100Kgf/cm2で押し出
し成形し、該押出成形体を気中にて1日間養生
し、予備的水和硬化を行つた。然る後に、フリツ
トを主成分とする通常の釉薬をスプレー法により
塗布し、焼成温度900℃、保持時間30分で焼成し
た。そして、該焼成体を蒸気養生にて3日間養生
し、本格的水和硬化を行つた。本格的水和硬化後
の試験片の大きさは、100mm×150mm×10mmであ
る。
``Purpose of the Invention'' [Industrial Field of Application] The present invention involves applying a glaze to the surface of a molded product obtained by extruding a mixture of raw materials mainly consisting of cement, fiber, and water, and then firing the product. The present invention relates to a method for manufacturing a glazed cement product in which a glaze layer is formed by forming a glaze layer. [Prior art] Normally, when manufacturing glazed cement products by extrusion, the main components are cement such as ordinary Portland cement, early strength cement, and blast furnace slag cement (hereinafter simply referred to as cement), fiber, and water. Aggregates and additives are added and mixed as necessary to the mixture, and the mixture is extruded and the surface of the molded body is glazed, followed by firing and hydration hardening to produce a product. In this case, the fiber is extrudable,
This is to improve shape retention, and asbestos fiber is generally used. The aggregates used include silica sand, hard sandstone, river sand, crushed ceramic tiles and sanitary ware, and the additives include plasticizers, water-reducing materials, and expansion materials. [Problems to be Solved by the Present Invention] The conventional method for manufacturing the above-mentioned glazed cement products by extrusion molding had the following drawbacks.
In other words, (1) Since the fiber used as the main component is asbestos fiber, pinholes may remain in the glaze layer of the product, which impairs the aesthetic appearance, lacks frost resistance, and significantly reduces the value of the product. It has the disadvantage of reducing the (2) Also included in asbestos fibers during firing.
When a small amount of Mg is dissolved in solid solution, α'-C 2 S is generated, which has the disadvantage that the development of mechanical strength during subsequent hydration hardening is delayed. The inventors investigated the cause of these shortcomings and found the following. In other words, the drawback of (1) above is that chrysotile asbestos (3MgO・2SiO 2・2H 2 O) used as asbestos fiber does not
At around 600℃, it gradually starts dehydrating and begins to disintegrate. However, commonly used glazes begin to soften at around 600°C and melt at around 700-900°C. Since the softening temperature of this glaze and the dehydration temperature of the asbestos fibers are almost the same, the water that evaporates on the surface of the object to be fired (extruded object) due to dehydration softens and becomes a continuous layer with high viscosity. It becomes encapsulated within the glaze layer of the state. Moreover, even if the glaze is completely melted during subsequent high-temperature firing, its viscosity does not decrease like water, and the water that is once encapsulated in the softened glaze layer remains without being removed.
As a result, pinholes were generated, the aesthetic appearance was impaired, and the frost damage resistance was also poor. Furthermore, the above drawback (2) is based on the inherent properties of glazed cement products. Generally, in the case of this type of glazed cement product, when the cement extrusion molded body is glazed and fired, the cement hydrate is dehydrated and C 2 S and CS are generated. For this reason, the fired body has the property that although its mechanical strength once decreases, the strength is recovered by subsequent hydration hardening. However, C 2 S and CS have the property that strength development is slow and strength recovery takes time. This tendency differs depending on the various transformations of C 2 S, and in particular, α'-C 2 S, which is produced by a small amount of solid solution of Mg in asbestos fibers during the firing process, has a remarkable tendency. It was hot. This drawback is that when manufacturing glazed cement products by extrusion, asbestos fibers are mixed with other cements,
This was unavoidable since it is the main component along with water. In addition, recently, substances precipitated from various chemical products have become a public pollution problem. Even in the case of extrusion-molded glazed cement products using asbestos fibers, asbestos fibers have been problematic as carcinogenic substances and substances that cause silicosis, etc., and their use has not been desirable. Conventionally, when producing glazed cement products by suction molding, asbestos fibers have been used in the same way as in extrusion molding, which has the above-mentioned drawbacks. ``Structure of the Invention'' [Means for Solving the Problems] The present invention solves the above-mentioned drawbacks of the conventional technology by extrusion molding a mixture of raw materials mainly composed of cement, fiber, and water. When producing a glazed cement product with excellent mechanical strength by applying a glaze to the surface of the obtained molded body, firing it at high temperature, and then hydration hardening, the fibers are vinylon fibers. , organic fibers such as acrylic fibers, carbon fibers, pulp fibers, etc., whose burnout temperature is 500℃ lower than the melting temperature of normal glazes.
The fibers are burned out by heating the molded body once to a fiber burning temperature or heating to the fiber burning temperature during glaze firing, and then fired at a temperature of 650 to 900°C, It is an object of the present invention to provide a method for manufacturing a glazed cement product in which the fired body is hydrated and hardened. This results in
There are no pinholes in the glaze layer, making it possible to create a product with excellent aesthetics and frost damage resistance, as well as excellent early development of mechanical strength. As mentioned above, the method of the present invention can be applied to cement, fiber,
The main component is water. Therefore, the cement includes commonly used cements such as ordinary Portland cement, alumina cement, blast furnace slag cement, mixed cement, and early strength cement (hereinafter referred to as
(simply referred to as cement). In addition, fibers include organic fibers such as vinylon fibers and acrylic fibers, carbon fibers, pulp fibers, etc.
Any material that can be burnt out at a temperature of ℃ or lower is acceptable. Materials used in addition to the above-mentioned main components include thickeners, aggregates, and additives such as water reducing agents, hardening accelerators, hardening retarders, and colorants. As the thickener, methylcellulose, ethylcellulose, carboxymethylcellulose, polyethylene oxide, polyvinyl alcohol, etc. are used. Particularly preferred is methylcellulose. Furthermore, as the aggregate, those commonly used as aggregates for cement, such as sand, sieruben, and siyamoto, are sufficient.
Additives such as water reducing agents, curing accelerators, curing retarders, and coloring agents are used as necessary. In the method of the present invention, the above-mentioned materials are placed in a conventional mixer and mixed. Then, if necessary, the mixture is kneaded using a predetermined kneader. next,
The kneaded or unkneaded mixture is extruded into a predetermined shape using an extrusion molding machine. After that, the extruded product is immersed in air or water for several hours.
Perform preliminary hydration curing for several days. After preliminary hydration and hardening, a desired surface of the extruded molded product is glazed with a conventional glaze raw material containing glass powder or frit as a main component by spraying, curtaining, dipping, or the like. Next, the glazed extrusion molded body is heated to a fiber burning-off temperature to burn out the aforementioned fibers contained in the molded body. This heating may be performed separately from the later firing, or may be performed simultaneously. The heating at this fiber burning-off temperature is below the melting temperature of the glaze, and when the fibers are burned off, water does not dissolve into the glaze. In other words, it does not cause pinholes. After that, the extruded body is fired at a temperature of 650 to 900°C. In the present invention, since asbestos fibers are not used unlike in the past, α'-C 2 S is not produced during firing. Therefore, the strength development during the full-scale hydration hardening performed later is not delayed by α'-C 2 S, and the strength can be recovered quickly. After firing, the fired body is cooled and full-scale hydration hardening is performed by curing such as immersion in water, steam curing, and autoclave curing. Incidentally, the portion where the fibers are burned away becomes a bore, but this is not a problem because the cement hydrate during the full-scale hydration hardening that is performed thereafter fills this bore. However, if the diameter of the fibers is large, even cement hydrate may not be able to fill the above-mentioned bores, so the diameter of the fibers used is
It is desirable that the thickness is 100 μm or less. After full-scale hydration hardening is completed, it can be taken out and dried. As a result, it is possible to obtain a glazed cement product that does not have pinholes in the glaze layer and has excellent early development of strength. In order to further improve the mechanical strength, metal fibers such as steel fibers and stainless fibers, and heat-resistant fibers such as ceramic fibers may be added at the time of mixing the raw materials. This heat-resistant fiber does not melt or soften even at the firing temperature of the glaze, and does not cause pinholes or the like. Furthermore, a metal reinforcing material such as a metal wire, a material framed by metal wires, or a metal mesh may be buried during extrusion molding. If this metal reinforcing material and the above-mentioned heat-resistant fiber are used together, extremely excellent mechanical strength can be obtained. Next, specific examples will be described in which a glazed cement product manufactured by the method of the present invention is compared with a glazed cement product manufactured by a conventional method. [Example] Comparative products were manufactured using both the present invention and the conventional method.
The raw materials shown in Table 1 were mixed using a mixer OM-30 manufactured by Chiyoda Giken Kogyo Co., Ltd., and then
The mixture was kneaded using a kneader PAD-3 manufactured by Co., Ltd. Then, the mixture after kneading was extruded using an extrusion molding machine DE-100 manufactured by Honda Iron Works Co., Ltd. at a molding pressure of 100 Kgf/cm 2 , and the extruded product was cured in air for 1 day to prepare a preliminary Hydration curing was performed. Thereafter, a conventional glaze containing frit as a main component was applied by spraying, and the material was fired at a firing temperature of 900°C for a holding time of 30 minutes. Then, the fired body was cured by steam curing for 3 days to perform full-scale hydration hardening. The size of the test piece after full-scale hydration hardening is 100 mm x 150 mm x 10 mm.

【表】 また表−2は、上述の要領で製造した本発明品
と従来品との比較結果を示すものである。
[Table] Table 2 shows the results of comparison between the product of the present invention manufactured in the manner described above and the conventional product.

【表】【table】

【表】 この表−2から明らかな如く、本発明品はピン
ホールの発生がなく、強度的にも優れている。そ
れに、焼成後の本格的水和硬化時における強度回
復の遅延原因となるα′−C2Sも生成されることは
ない。従つて、図面に示す如く、本発明品は強度
の早期発現性という点で優れている。 尚、本発明の技術はサクシヨン成形法で施釉セ
メント製品を製造する場合へも適用でき、この場
合も上述の押出成形の場合と同様の効果を得るこ
とが可能である。 『発明の効果』 以上説明したように本発明によれば、製品の釉
薬面にピンホールの発生がなく、美観及び耐凍害
性に優れたものを得ることが可能である。また焼
成時にα′−C2Sが生成されないので、焼成後に行
われる本格的水和硬化時の早期強度回復が得られ
る。それにより、本発明では石綿繊維を全く使用
していないので、石綿自体の持つ発ガン性、ケイ
肺等の公害問題が起こることもない。
[Table] As is clear from Table 2, the products of the present invention do not generate pinholes and are excellent in strength. In addition, α′-C 2 S, which causes a delay in strength recovery during full-scale hydration hardening after firing, is not generated. Therefore, as shown in the drawings, the product of the present invention is excellent in terms of early development of strength. The technique of the present invention can also be applied to the production of glazed cement products using the suction molding method, and in this case as well, it is possible to obtain the same effects as in the case of extrusion molding described above. [Effects of the Invention] As explained above, according to the present invention, it is possible to obtain a product with no pinholes on the glazed surface and with excellent aesthetic appearance and frost damage resistance. Furthermore, since α'-C 2 S is not generated during firing, early strength recovery can be achieved during full-scale hydration hardening after firing. As a result, since the present invention does not use asbestos fibers at all, pollution problems such as carcinogenicity and silicosis, which asbestos itself has, do not occur.

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

図面は本発明品と従来品の強度回復状況を示す
図面である。
The drawing shows the strength recovery status of the product of the present invention and the conventional product.

Claims (1)

【特許請求の範囲】[Claims] 1 セメント、繊維、水を主成分とする原料の混
合物を押し出し成形し、得られた成形体の表面
に、釉薬を塗布して高温焼成し、その後水和硬化
させることで機械的強度に優れた施釉セメント製
品を製造する場合にあつて、前記繊維は、ビニロ
ン繊維、アクリル繊維等の有機繊維や炭素繊維若
しくはパルプ繊維等であつて、その焼失温度が通
常の釉薬の溶融温度よりも低い500℃以下であり、
前記成形体を一旦繊維焼失温度で加熱するか若し
くは釉薬焼成時にあつて該繊維焼失温度まで加熱
することで前記繊維を焼失させ、然る後に650〜
900℃の温度で焼成し、該焼成体を水和硬化させ
ることを特徴とする施釉セメント製品の製造方
法。
1 A mixture of raw materials mainly composed of cement, fiber, and water is extruded and molded, and the surface of the resulting molded product is coated with glaze, fired at high temperature, and then cured by hydration, resulting in a product with excellent mechanical strength. In the case of manufacturing glazed cement products, the fibers are organic fibers such as vinylon fibers and acrylic fibers, carbon fibers, pulp fibers, etc., and the burnout temperature is 500 ° C., which is lower than the melting temperature of ordinary glazes. The following is
The fibers are burned out by heating the molded body once to the fiber burning temperature, or by heating to the fiber burning temperature during glaze firing, and then
A method for producing a glazed cement product, which comprises firing at a temperature of 900°C and hydrating and hardening the fired product.
JP12953284A 1984-06-22 1984-06-22 Manufacture of glazed cement product Granted JPS6117464A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12953284A JPS6117464A (en) 1984-06-22 1984-06-22 Manufacture of glazed cement product

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12953284A JPS6117464A (en) 1984-06-22 1984-06-22 Manufacture of glazed cement product

Publications (2)

Publication Number Publication Date
JPS6117464A JPS6117464A (en) 1986-01-25
JPH0411499B2 true JPH0411499B2 (en) 1992-02-28

Family

ID=15011841

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12953284A Granted JPS6117464A (en) 1984-06-22 1984-06-22 Manufacture of glazed cement product

Country Status (1)

Country Link
JP (1) JPS6117464A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1217463B (en) * 1988-05-02 1990-03-22 Bayer Italia Spa PROCEDURE FOR THE PRODUCTION OF CERAMIC GLAZES AGGLOMERATED THROUGH EXTRUSION, GLAZES SO OBTAINED F ENAMELED ENAMELS WITH THEM

Also Published As

Publication number Publication date
JPS6117464A (en) 1986-01-25

Similar Documents

Publication Publication Date Title
CN101244951B (en) Glaze composition
US4407769A (en) Method of manufacturing cement products having superior mechanical strength
JPH0225876B2 (en)
JPH0411499B2 (en)
KR940000727B1 (en) Cement-containing ceramic articles and method for production thereof
JPH04175281A (en) Glazed molded article of cement having transfer decoration and production thereof
JP3491991B2 (en) Manufacturing method of cement-based fired building materials
JPH0624875A (en) Sanitary ware using cement composition and production thereof
JPH0280363A (en) Ceramics product which prevents efflorescence and its production
JPH05279097A (en) Heat resistant cement composition
JP3930752B2 (en) Large ceramic plate for building material and method for producing the same
KR930005252B1 (en) High-strength ceramic materials and methods for making same
JP3181968B2 (en) Manufacturing method of enamel concrete
JPS59141476A (en) Manufacture of cement products
JPS61205654A (en) Superhigh strength cement concrete composition
JPH0624876A (en) Production of terracotta
JPH0741357A (en) Manufacturing method of fired board for construction
JPS62223080A (en) Manufacture of inorganic hardened body
JP2633065B2 (en) Glazing method
JP2802242B2 (en) Manufacturing method of glazed cement products
CN120208681A (en) A novel composite furnace door glaze prefabricated part and its preparation method
JPS62223079A (en) Manufacture of inorganic hardened body
KR870000655B1 (en) Manufacturing method of cement product with excellent mechanical strength
JPH0214307B2 (en)
JPH06191964A (en) Production of lightweight burned body