JPH032827B2 - - Google Patents

Info

Publication number
JPH032827B2
JPH032827B2 JP15431486A JP15431486A JPH032827B2 JP H032827 B2 JPH032827 B2 JP H032827B2 JP 15431486 A JP15431486 A JP 15431486A JP 15431486 A JP15431486 A JP 15431486A JP H032827 B2 JPH032827 B2 JP H032827B2
Authority
JP
Japan
Prior art keywords
glaze
calcium silicate
viscosity
weight
glazed
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
JP15431486A
Other languages
Japanese (ja)
Other versions
JPS6325283A (en
Inventor
Tetsuya Koide
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.)
Inax Corp
Original Assignee
Inax Corp
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 Inax Corp filed Critical Inax Corp
Priority to JP15431486A priority Critical patent/JPS6325283A/en
Publication of JPS6325283A publication Critical patent/JPS6325283A/en
Publication of JPH032827B2 publication Critical patent/JPH032827B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Aftertreatments Of Artificial And Natural Stones (AREA)

Description

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

[産業上の利用分野] 本発明は施釉珪酸カルシウム体の製法に係り、
特にゾノトライト質珪酸カルシウム板の表面に剥
離しにくく、かつ硬質なセラミツク被覆を形成す
る方法に関する。 [従来の技術] ゾノトライト質珪酸カルシウム板は、軽量で耐
火性に優れる等の特長を有し、従来より断熱材等
として有効に使用されている。 [発明が解決しようとする問題点] 従来、表面化粧されたゾノトライト質珪酸カル
シウム板は提供されておらず、ゾノトライト質珪
酸カルシウム板を断熱材等として建築物等に使用
する場合には、その施工面上に更に表面仕上げ材
を施工する必要があり、施工工数が多く、作業が
煩雑であるなどの欠点があつた。 [問題点を解決するための手段] 本発明は上記実情に鑑み、ゾノトライト質珪酸
カルシウム成形体に良好な表面化粧を施す方法を
提供するべくなされたものであつて、全固型分量
に対する全水量が65〜76重量%で、かつ粘度が
1000〜8500cpである釉薬を、ゾノトライト質珪
酸カルシウム成形体に施釉し、次いで100〜150℃
で乾燥した後、最高温度800〜1000℃で0.1〜10時
間焼成することを特徴とする施釉珪酸カルシウム
体の製法、を要旨とするものである。 即ち、本発明者らは、まず、表面仕上げ材とし
て、耐久性に優れ、かつ非常に美麗であり、高級
感を感じさせるものに釉薬を施されたタイルがあ
ることから、ゾノトライト質珪酸カルシウム成形
体の上にこの釉薬を施すことができれば、断熱材
等としても優れ、かつ、高級感のある表面美麗な
極めて優れた建築材料が得られるものと推察し
た。 そこで、ゾノトライト質珪酸カルシウム成形体
に釉薬処理を施した施釉珪酸カルシウム体を製造
する方法について検討したが、陶磁器質タイルの
場合には、施釉する時点での成形体吸水率は5〜
15%程度であるのに対し、ゾノトライト質珪酸カ
ルシウム成形体は、150〜200%の吸水率を有する
ため、通常の陶磁器質タイルに施す釉薬をそのま
ま適用することができないという難点が見出され
た。即ち、通常の釉薬をそのまま適用した場合に
は、良好な施釉面が得られず、亀裂、ピンホール
発生等は避けられない。本発明者らは、このよう
な点について更に研究を重ねた結果、特定の水分
量で特定粘度の釉薬であればゾノトライト質珪酸
カルシウム成形体に良好に適用できることを見出
し、本発明を完成させた。 以下に本発明を詳細に説明する。 本発明において、施釉処理するゾノトライト質
珪酸カルシウム成形体は、常法により、珪酸質原
料粉末、石灰質原料粉末、水、必要に応じて耐火
粘土、石綿、バインダ等を混練し、成形、養生し
てゾノトライトを生成させることにより、容易に
製造することができる。この場合、成形法として
は、公知の抄造法、押出法、プレス成形法等のい
ずれも採用可能である。 本発明の方法においては、このようにして得ら
れたゾノトライト質珪酸カルシウム成形体に施す
釉薬として、全固型分量に対する全水量が65〜76
重量%で、かつ粘度が1000〜8500cpである釉薬
を用いる。 釉薬の全固型分量に対する全水量が65重量%未
満あるいは粘度が8500cpを超えると、平滑な施
釉面が得られず、ピンホール等が多量に発生する
ようになり好ましくない。一方、釉薬の全固型分
量に対する全水量が76重量%よりも多い場合ある
いは粘度が1000cp未満の場合には、釉薬が側面
側へタレ、著しい場合には裏面側にもまわつてし
まい、良好な施釉を行うことができない。このた
め、本発明においては上記範囲の水分量及び粘度
の釉薬を用いる。 このような釉薬は通常の釉薬の調整法におい
て、水分量を適宜調整することにより容易に製造
することができる。 ところで、本発明で用いる、全固型分量に対す
る全水量が65〜76重量%で、かつ粘度が1000〜
8500cpの釉薬は、水分量が多く粘性が小さいこ
とから固型分粒子の沈降速度が速く、長期間安定
に保存することが困難であるため、大量生産には
必ずしも好適とはいえない。 このため、本発明の実施にあたつては、予め、
比較的水分量が少なく粘性の高い、安定な釉薬を
調製しておき、施釉する直前にこの釉薬に水を加
えて再混練し、上記範囲の水分量及び粘度を有す
る釉薬を調製して用いるのが好ましい。この場
合、予め調製しておく釉薬としては、全固型分量
に対する全水量が62重量%以下で、かつ粘度が
13000cp以上のものが、その安定性、使用時に水
を加えた時の混練性、釉薬特性の再現性等から特
に好ましい。 本発明においては、釉薬をゾノトライト質珪酸
カルシウム成形体にスプレー、刷毛塗り等により
施釉した後、100〜150℃で乾燥し、次いで最高温
度800〜1000℃で0.1〜10時間焼成する。特に、本
発明においては、100〜150℃で3時間以上の乾燥
を行つた後、800〜1000℃で焼成を行うことによ
り、極めて美麗で高特性の施釉珪酸カルシウム体
を製造することができる。なお、ゾノトライト質
珪酸カルシウム成形体は、780℃付近でワラスト
ナイト質に結晶形が変化するが、建築材料として
要求される軽量性、耐火性等の特性については、
何ら影響を受けることはない。 [実施例] 以下、実施例について説明する。 実施例 1 フリツト釉100重量部、粘土5重量部及び第1
表に示す量の水を、各々ポツトミルにとり、2〜
3時間混合し、更にCMC2重量%溶液を20重量部
加えて1〜2時間混合して、第1表に示す全水量
及び粘度の釉薬No.1〜No.10を調製した。この釉薬
No.1〜No.10を、各々、ゾノトライト質珪酸カルシ
ウム成形体にスプレーにて施釉し、120℃で3時
間乾燥した後、950℃で1時間焼成した。各々の
施釉後の表面の状況と焼成後の表面の状態の観察
結果を第1表に示す。
[Industrial Application Field] The present invention relates to a method for producing a glazed calcium silicate body,
In particular, the present invention relates to a method of forming a hard ceramic coating on the surface of a xonotrite calcium silicate plate that is hard to peel off and is hard. [Prior Art] Zonotrite calcium silicate plates have features such as being lightweight and having excellent fire resistance, and have been effectively used as heat insulating materials and the like. [Problems to be Solved by the Invention] Hitherto, surface-decorated zonotritic calcium silicate plates have not been provided, and when zonotritic calcium silicate plates are used in buildings as heat insulating materials, etc., it is difficult to install them. There were drawbacks such as the need to further apply a surface finishing material on the surface, requiring a large number of construction steps and making the work complicated. [Means for Solving the Problems] In view of the above-mentioned circumstances, the present invention has been made to provide a method for applying a good surface decoration to a xonotrite calcium silicate molded body, and the present invention is to provide a method for applying a good surface decoration to a xonotrite calcium silicate molded body. is 65 to 76% by weight, and the viscosity is
A glaze of 1000~8500cp is applied to a xonotrite calcium silicate molded body, and then heated at 100~150℃.
The gist of this invention is a method for producing a glazed calcium silicate body, which is characterized by drying the body at a temperature of 800 to 1000°C and then firing it for 0.1 to 10 hours. That is, the present inventors first used xonotrite calcium silicate molding as a surface finishing material because glazed tiles are highly durable, very beautiful, and give a sense of luxury. It was surmised that if this glaze could be applied to the body, it would be possible to obtain an extremely excellent building material that is excellent as a heat insulator and has a beautiful surface with a luxurious feel. Therefore, we investigated a method for producing a glazed calcium silicate body by applying a glaze treatment to a zonotrite calcium silicate molded body, but in the case of ceramic tiles, the water absorption rate of the molded body at the time of glazing is 5 to 5.
In contrast, xonotrite calcium silicate moldings have a water absorption rate of 150 to 200%, so it was found difficult to apply the glaze applied to ordinary ceramic tiles as is. . That is, if a normal glaze is applied as is, a good glazed surface cannot be obtained, and cracks, pinholes, etc. are unavoidable. As a result of further research on these points, the present inventors found that a glaze with a specific moisture content and a specific viscosity can be well applied to a xonotrite calcium silicate molded body, and completed the present invention. . The present invention will be explained in detail below. In the present invention, the zonotrite calcium silicate molded body to be glazed is prepared by kneading silicic raw material powder, calcareous raw material powder, water, and if necessary fireclay, asbestos, binder, etc., molding, and curing. It can be easily manufactured by producing xonotlite. In this case, as the molding method, any of the known paper forming methods, extrusion methods, press molding methods, etc. can be employed. In the method of the present invention, the glaze applied to the thus obtained xonotrite calcium silicate molded body has a total water content of 65 to 76% of the total solid content.
% by weight and a viscosity of 1000 to 8500 cp is used. If the total amount of water based on the total solid content of the glaze is less than 65% by weight or if the viscosity exceeds 8,500 cp, a smooth glazed surface will not be obtained and a large number of pinholes will occur, which is undesirable. On the other hand, if the total water content relative to the total solid content of the glaze is more than 76% by weight or if the viscosity is less than 1000 cp, the glaze will drip to the sides, or in severe cases, it will even spread to the back side, resulting in a good product. Cannot be glazed. Therefore, in the present invention, a glaze having a water content and viscosity within the above range is used. Such a glaze can be easily produced by appropriately adjusting the water content in a normal glaze preparation method. By the way, the total amount of water relative to the total solid content used in the present invention is 65 to 76% by weight, and the viscosity is 1000 to 1000.
The 8500 cp glaze is not necessarily suitable for mass production because it has a high water content and low viscosity, so the solid particles settle at a high rate, making it difficult to store stably for a long period of time. Therefore, in implementing the present invention, in advance,
A stable glaze with a relatively low water content and high viscosity is prepared, and just before glazing, water is added to this glaze and kneaded again to prepare a glaze with a water content and viscosity within the above range. is preferred. In this case, the glaze prepared in advance must have a total water content of 62% by weight or less based on the total solid content, and a viscosity of
A glaze of 13,000 cp or more is particularly preferred from the viewpoint of stability, kneading ability when water is added during use, reproducibility of glaze characteristics, etc. In the present invention, a xonotrite calcium silicate molded body is glazed with a glaze by spraying, brushing, etc., then dried at 100 to 150°C, and then fired at a maximum temperature of 800 to 1000°C for 0.1 to 10 hours. In particular, in the present invention, by drying at 100 to 150°C for 3 hours or more and then firing at 800 to 1000°C, it is possible to produce a glazed calcium silicate body that is extremely beautiful and has high properties. Note that the crystal shape of the xonotrite calcium silicate molded body changes to wollastonite at around 780℃, but the characteristics such as lightness and fire resistance required as a building material are
It will not be affected in any way. [Example] Examples will be described below. Example 1 100 parts by weight of fritted glaze, 5 parts by weight of clay and the first
Add the amount of water shown in the table to each pot mill, and
After mixing for 3 hours, 20 parts by weight of CMC 2% by weight solution was added and mixed for 1 to 2 hours to prepare glazes No. 1 to No. 10 having the total water amount and viscosity shown in Table 1. This glaze
No. 1 to No. 10 were each glazed onto a xonotrite calcium silicate molded body by spraying, dried at 120°C for 3 hours, and then fired at 950°C for 1 hour. Table 1 shows the observation results of the surface condition after each glazing and after firing.

【表】 第1表より、明らかなように全固型分量に対す
る全水量が65〜76重量%で、粘度が1000〜
8500cpの釉薬(No.7〜10)を使用することによ
り、良好な施釉面を得ることができる。 実施例 2 実施例1で調整された釉薬No.1〜No.7を、
各々、ビーカーにとり、20℃で静置してその安定
性を調べた。結果を第2表に示す。 第2表より、No.3〜No.7の全水量が62重量%を
超える釉薬では、粒子の沈降が速く、静置7日以
後のものは、その沈降量が極めて多いことが明ら
かである。しかして、これらのものは、再度撹拌
しても元の状態には戻らず、異質の釉薬に変性し
ていた。 これに対して、全水量62重量%以下、粘度
13000cp以上のもの(No.1、No.2)であれば、長
期間安定に保存できることが確認された。
[Table] From Table 1, it is clear that the total amount of water relative to the total solid content is 65-76% by weight, and the viscosity is 1000-1000%.
By using 8500 cp glaze (No. 7 to 10), a good glazed surface can be obtained. Example 2 Glazes No. 1 to No. 7 prepared in Example 1 were
Each sample was placed in a beaker and allowed to stand at 20°C to examine its stability. The results are shown in Table 2. From Table 2, it is clear that in the glazes No. 3 to No. 7 with a total water content exceeding 62% by weight, the particles settle quickly, and the amount of sedimentation is extremely large after 7 days of standing. . However, even if these glazes were stirred again, they did not return to their original state and had denatured into a foreign glaze. In contrast, the total water content is 62% by weight or less, the viscosity is
It was confirmed that items of 13,000 cp or higher (No. 1, No. 2) can be stored stably for a long period of time.

【表】 実施例 3 実施例1で調整したNo.1の釉薬、即ち、下記組
成及び物性の釉薬を、各々、第3表に示す期間静
置し、これに、ゾノトライト質珪酸カルシウム成
形体に施釉する直前に、13.75重量部の水を加え
て再混練し、第3表に示す全水量及び粘度の釉薬
とし、この釉薬を用いてスプレーにより施釉を行
つた。 釉薬No.1 フリツト 100重量部 粘 土 4 〃 水 40 〃 CMC2%溶液 20 〃 全水量 57.1重量% 粘 度 27500cp この場合の、施釉作業性と施釉後の施釉面の状
況を第3表に示す。 第3表より、全水量62重量%以下、粘度
13000cp以上の釉薬を作成しておき、これを使用
する直前に、水を加えて再混練することにより、
良好な再現性のもとに、本発明で特定する全水量
及び粘度の釉薬を得ることができることが明らか
である。 なお、得られた施釉ゾノトライト質珪酸カルシ
ウム成形体を120℃で8時間乾燥し、最高温度900
℃で60分間保持して焼成したところ、いずれも極
めて美麗な施釉面を有する施釉珪酸カルシウム体
を得ることができた。
[Table] Example 3 The No. 1 glaze prepared in Example 1, that is, the glaze with the following composition and physical properties, was allowed to stand for the period shown in Table 3, and then applied to a xonotrite calcium silicate molded body. Immediately before glazing, 13.75 parts by weight of water was added and kneaded again to obtain a glaze having the total water amount and viscosity shown in Table 3, and glaze was applied by spraying using this glaze. Glaze No. 1 Fritz 100 parts by weight Clay 4 Water 40 CMC 2% solution 20 Total water 57.1% by weight Viscosity 27500cp Table 3 shows the workability of glazing and the condition of the glazed surface after glazing. From Table 3, total water content is 62% by weight or less, viscosity
Create a glaze of 13000 cp or more, and just before using it, add water and knead it again.
It is clear that glazes with the total water content and viscosity specified in the present invention can be obtained with good reproducibility. The obtained glazed zonotrite calcium silicate molded body was dried at 120°C for 8 hours, and the maximum temperature was 900°C.
When the materials were held at ℃ for 60 minutes and fired, glazed calcium silicate bodies with extremely beautiful glazed surfaces could be obtained.

【表】 [発明の効果] 以上詳述した通り、本発明の施釉珪酸カルシウ
ム体の製法は、全固型分量に対する全水量が65〜
76重量%で、かつ粘度が1000〜8500cpである釉
薬を、ゾノトライト質珪酸カルシウム成形体に施
釉し、次いで100〜150℃で乾燥した後、最高温度
800〜1000℃で0.1〜10時間焼成するものであつ
て、軽量かつ耐火性等に優れ、建材等として極め
て有用なゾノトライト質珪酸カルシウム成形体に
良好な施釉作業性のもとに容易に施釉面を形成す
ることができる。しかして、形成された施釉面は
極めて平滑性に優れ、ピンホールや割れ等の発生
もなく、極めて良好な特性を有する。しかも、施
釉にあたつては、釉薬の水分量と粘性を管理する
ため、釉薬の品質が安定化し、釉薬のロツトによ
る製品品質のバラツキもない。 従つて、本発明によれば、ゾノトライト質の美
麗な表面化粧材を得ることができ、建材等として
適用する場合、施工作業性は著しく改善される。
[Table] [Effects of the Invention] As detailed above, the method for producing the glazed calcium silicate body of the present invention is such that the total water content relative to the total solid content is 65 to 65%.
A glaze of 76% by weight and a viscosity of 1000 to 8500 cp is applied to a xonotlitic calcium silicate molded body, then dried at 100 to 150°C, and then heated to the maximum temperature.
It is fired at 800 to 1000℃ for 0.1 to 10 hours, and can easily glaze zonotrite calcium silicate molded bodies, which are lightweight, have excellent fire resistance, and are extremely useful as building materials, etc., with good glazing workability. can be formed. The glazed surface thus formed is extremely smooth, free of pinholes, cracks, etc., and has extremely good properties. Furthermore, since the water content and viscosity of the glaze are controlled during glazing, the quality of the glaze is stabilized and there is no variation in product quality due to glaze lots. Therefore, according to the present invention, a beautiful xonotrite surface decorative material can be obtained, and when applied as a building material, workability is significantly improved.

Claims (1)

【特許請求の範囲】 1 全固型分量に対する全水量が65〜76重量%
で、かつ粘度が1000〜8500cpである釉薬を、ゾ
ノトライト質珪酸カルシウム成形体に施釉し、次
いで100〜150℃で乾燥した後、最高温度800〜
1000℃で0.1〜10時間焼成することを特徴とする
施釉珪酸カルシウム体の製法。 2 全固型分量に対する全水量が62重量%以下
で、かつ粘度が13000cp以上の釉薬に、施釉直前
に水を加えて混練し、全固型分量に対する全水量
が65〜75重量%で、かつ粘度が1000〜8500cpで
ある釉薬とし、これを前記ゾノトライト質珪酸カ
ルシウム成形体に施釉することを特徴とする特許
請求の範囲第1項に記載の製法。
[Claims] 1. The total amount of water relative to the total solid content is 65 to 76% by weight.
A glaze with a viscosity of 1000 to 8500 cp is applied to a xonotrite calcium silicate molded body, then dried at 100 to 150°C, and then heated to a maximum temperature of 800 to 850°C.
A method for producing a glazed calcium silicate body, which is characterized by firing at 1000°C for 0.1 to 10 hours. 2 Add water to a glaze with a total water content of 62% by weight or less based on the total solid content and a viscosity of 13,000 cp or more just before glazing, and knead it to create a glaze with a total water content of 65 to 75% by weight based on the total solid content, and The manufacturing method according to claim 1, characterized in that the xonotrite calcium silicate molded body is glazed with a glaze having a viscosity of 1000 to 8500 cp.
JP15431486A 1986-07-01 1986-07-01 Manufacture of glazed calcium silicate body Granted JPS6325283A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15431486A JPS6325283A (en) 1986-07-01 1986-07-01 Manufacture of glazed calcium silicate body

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15431486A JPS6325283A (en) 1986-07-01 1986-07-01 Manufacture of glazed calcium silicate body

Publications (2)

Publication Number Publication Date
JPS6325283A JPS6325283A (en) 1988-02-02
JPH032827B2 true JPH032827B2 (en) 1991-01-17

Family

ID=15581409

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15431486A Granted JPS6325283A (en) 1986-07-01 1986-07-01 Manufacture of glazed calcium silicate body

Country Status (1)

Country Link
JP (1) JPS6325283A (en)

Also Published As

Publication number Publication date
JPS6325283A (en) 1988-02-02

Similar Documents

Publication Publication Date Title
KR101149576B1 (en) Manufacturing method for clay brick and clay brick
KR100408756B1 (en) Dressing body composition used for clay bricks
JPH032827B2 (en)
JP2962423B2 (en) Glazed compact, method for producing glaze compact and method for producing glaze compact
JPH0450183A (en) Formed cement product and production thereof
SU1680651A1 (en) Raw mixture for obtaining lining material
KR100610657B1 (en) Manufacturing method of artificial wood panel using ceramic composition for artificial wood and ceramic composition for artificial wood
JP2813391B2 (en) Glazed lightweight ceramic product and method for producing the same
SU1288173A1 (en) Method of manufacturing decorative ceramic members
JPH04954B2 (en)
JPH01301547A (en) Production of cement product
CN1669987A (en) Gemstone ceramic sintering agent and method for manufacturing gemstone ceramic products
JPH0328183A (en) Production of blazed cement product
SU1186586A1 (en) Method of manufacturing decorative facing material
JPH0424315B2 (en)
JP2633065B2 (en) Glazing method
JPH075349B2 (en) Method for manufacturing ceramic sintered products using anti-fire stone
JPH0416544A (en) Body composition for large-sized porcelain and production of large-sized porcelain
JPH032830B2 (en)
JPS63315546A (en) Production of flexible cement-based sheet
JPH0254291B2 (en)
JPH01246186A (en) Colored concrete block
JPH02149484A (en) Production of glazed concrete panel
JPH0214864A (en) Production of decorative tile
JPH01100042A (en) Production of enameled cement product