JPH032831B2 - - Google Patents
Info
- Publication number
- JPH032831B2 JPH032831B2 JP23800286A JP23800286A JPH032831B2 JP H032831 B2 JPH032831 B2 JP H032831B2 JP 23800286 A JP23800286 A JP 23800286A JP 23800286 A JP23800286 A JP 23800286A JP H032831 B2 JPH032831 B2 JP H032831B2
- Authority
- JP
- Japan
- Prior art keywords
- heat insulating
- glazed
- base material
- insulating layer
- mixture
- 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
- 239000000203 mixture Substances 0.000 claims description 24
- 239000000378 calcium silicate Substances 0.000 claims description 18
- 229910052918 calcium silicate Inorganic materials 0.000 claims description 18
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 claims description 18
- 239000004570 mortar (masonry) Substances 0.000 claims description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
- 239000000126 substance Substances 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 239000012784 inorganic fiber Substances 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 238000001035 drying Methods 0.000 claims description 2
- 239000010410 layer Substances 0.000 description 37
- 239000000463 material Substances 0.000 description 36
- 239000002585 base Substances 0.000 description 28
- 238000000034 method Methods 0.000 description 21
- 238000010438 heat treatment Methods 0.000 description 11
- 239000000835 fiber Substances 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 239000004568 cement Substances 0.000 description 5
- 238000009413 insulation Methods 0.000 description 5
- 239000000758 substrate Substances 0.000 description 5
- 239000000853 adhesive Substances 0.000 description 4
- 230000001070 adhesive effect Effects 0.000 description 4
- 239000004576 sand Substances 0.000 description 4
- 229910019142 PO4 Inorganic materials 0.000 description 3
- 230000003139 buffering effect Effects 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 3
- 238000003825 pressing Methods 0.000 description 3
- 241000408495 Iton Species 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- 239000011398 Portland cement Substances 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 239000003638 chemical reducing agent Substances 0.000 description 2
- 239000004567 concrete Substances 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 239000010451 perlite Substances 0.000 description 2
- 235000019362 perlite Nutrition 0.000 description 2
- 229920002401 polyacrylamide Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 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
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000010425 asbestos Substances 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 239000011083 cement mortar Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 238000006703 hydration reaction Methods 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910001562 pearlite Inorganic materials 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229910052895 riebeckite Inorganic materials 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
Landscapes
- Aftertreatments Of Artificial And Natural Stones (AREA)
Description
イ 産業上の利用分野
本発明は施釉けい酸カルシウム成形体の製造方
法に関する。
ロ 従来の技術
施釉けい酸カルシウム成形体は、施釉面が美し
いこと、耐久性が良好なことから、建材例えば外
装材として注目されている。
施釉けい酸カルシウム成形体の製造方法は、け
い酸カルシウム成形体を基材(以下単に「基材」
という)とし、その表面の気孔を無くすため目止
めを行つたのち施釉する方法が採用されていた。
しかしこの方法は、施釉する際施釉面を加熱し、
その後冷却される際に、基材表層の被熱部とそれ
より深層の被熱されていない部分とで収縮率が異
るためその間に収縮亀裂が生じる。
一方、セメントモルタル(以下単に「モルタ
ル」という)表面に施釉した場合にはモルタルに
亀裂が生じないという従来の経験から、この技術
を応用した方法即ち基材にモルタルを塗布し施釉
する方法が試みられた。
しかしこの方法は、基材へのモルタルの接着性
の悪さから基材とモルタルとの界面(接着面)に
亀裂が発生し実用化にまで至らなかつた。
このように従来採用されていた方法のいずれに
おいても基材あるいは界面に亀裂が発生するとい
う欠点が解決されなかつた。
そこで本出願人は、亀裂の発生を抑制する手段
として、基材と施釉層との間に断熱層を設ける方
法即ち基材表面にリン酸塩系接着剤、パーライト
及び水の混練物を塗布し加熱硬化させて断熱層を
形成した後施釉する施釉けい酸カルシウム成形体
の製造方法を提案した(特開昭60−129566)。
ハ 発明が解決しようとする問題点
前記断熱層を形成する方法は亀裂の発生を抑制
でき一応の目的は達成した。
しかしながらこの方法は、製品を得るまでに、
リン酸塩系接着剤を硬化させ断熱層を形成させる
工程と釉薬を施釉する工程で2回の加熱冷却工程
を経なければならず、このように加熱冷却を繰り
返すため、それだけ工程は複雑でありエネルギー
ロスも大きいという欠点を有していた。
ニ 問題を解決するための手段
本発明者等は、断熱層を常温で形成し加熱冷却
工程は施釉工程の1回だけで済むようにすること
及び基材と施釉層との間に組成の異る2層の断熱
層を形成した後施釉することにより、基材や界面
に亀裂が発生しない施釉けい酸カルシウム成形体
が得られるとの知見を得て本発明に到達した。
即ち本発明は、けい酸カルシウム成形体(基
材)表面に水硬性物質、無機繊維、保水剤及び水
を混合した混合物を塗布して第1断熱層を形成し
た後、モルタル混練物を塗布して第2断熱層を形
成後硬化乾燥させてから施釉することを特徴とす
る施釉けい酸カルシウム成形体の製造方法にあ
る。
本発明において第1断熱層を設ける理由は、施
釉工程において第2断熱層の熱が基材へ伝わるの
を遮断し、基材と第2断熱層を一体化し、かつ第
1断熱層の熱膨張を吸収する緩衝作用をさせるた
めである。
本発明で使用する基材は、けい酸カルシウムで
つくられた成形体、例えば軽量気泡コンクリート
(ALC)をいう。
水硬性物質としてはポルトランドセメント、混
合セメント、超早硬性セメント等が挙げられる。
無機繊維は、断熱効果と緩衝効果とを高めるた
めに配合するもので、耐アルカリ性ガラス繊維、
炭素繊維、アルミナ繊維、鋼繊維、アスベスト等
の人工あるいは天然の無機系繊維が挙げられる。
保水剤は、繊維質混合物を基材表面に塗布した
際、水が基材に吸収されるのを防ぐために配合す
るもので、メチルセルロース(MC)、ヒドロキ
シエチルセルロース(HEC)、エチルヒドロキシ
エチルアルコール(EHEC)、ポリビニルアルコ
ール(PVA)、ポリエチレンオキサイド(PEO)、
ポリアクリルアミド(PAA)等が挙げられる。
尚、上記配合物のほか、例えば高融点の釉薬を
用いて施釉する場合や断熱層の厚さを薄くしなけ
ればならないような場合には、基材との接着性を
害さない程度に軽量骨材(例えばパーライト等)
を配合することは差し支えない。
次に、上記断熱層形成用原料の配合割合につい
て説明する。
無機繊維は、第1断熱層用として混合した混合
物全容積の0.5〜5.0vol%に配合するのが好まし
い。0.5vol%未満では断熱効果及び緩衝効果が小
さくなり、5.0vol%を超えると該繊維が分散しに
くくなり均一な混合が困難となる。
保水剤は、水硬性物質に対し0.05〜5.0wt%配
合する。0.05wt%未満では保水効果が弱く水が基
材に吸収されるので好ましくない。5.0wt%を超
えると水硬性物質の水和反応を阻害するので好ま
しくない。
水は、混合物が塗布できる柔らかさになる程度
に配合されていればよく、目安としては水硬性物
質に対して50〜300wt%である。50wt%未満だと
繊維質混合物が固く基材に塗布する作業が困難に
なり、300wt%を超えると流動性が大きすぎて所
定の厚さに塗布することが困難となる。
第2断熱層を設ける理由は、第1断熱層表面に
直接施釉すると第1断熱層表面に露出している繊
維類が加熱中に変色する等で意図しない模様の施
釉面ができたり、はなはだしい場合には見苦しい
模様ができたりするのを防ぐためと、表面強度を
向上させるためである。
第2断熱層に用いられる水硬性物質は前記第1
断熱層で用いられたものと同じである。
砂は市販の人工あるいは天然のものを用いる。
砂と水硬性物質との配合割合は通常の左官用モル
タルと同じであり、砂は水硬性物質に対して60〜
300wt%が好ましい。60wt%未満にすると富配合
モルタルとなるため硬化した際収縮が大きくな
り、微細な亀裂を発生する原因となるので好まし
くなく、逆に300wt%を超えると水セメント比が
大きくなりすぎ、強度が小さくなるので好ましく
ない。
水の配合量は混合物を塗布する作業ができる程
度の柔らかさになるように配合されていればよ
く、大体水硬性物質に対し30〜70wt%である。
30wt%未満では混合物が均一になりにくく塗布
作業もやりにくい。70wt%を超えると混練物の
流動性が大きくなりすぎて塗布作業が難しくなり
いずれも好ましくない。
尚、成形体の強度を確保するために、できるだ
け水量を減らしたり、気泡を減らしたりするのは
好ましいので、減水剤や消泡剤を適宜に配合する
ことは差し支えない。
第1及び第2断熱層の厚さは、施釉基材の所要
厚さになるようにすればよいが、少なくとも施釉
工程における加熱によつて基材に亀裂が入らない
ようにするためには、各断熱層とも3〜10mmの厚
さにするのが好ましい。
次に、本発明の施釉けい酸カルシウム成形体の
製造方法につき説明する。
所要寸法に加工された基材の表面に第1断熱層
用の繊維質混合物を鏝で充分に押し付けながら所
定の厚さに塗布した後、第2断熱層用のモルタル
混練物を、鏝で表面に気泡ができないように、か
つ平坦に所定厚さ塗布し硬化させる。
第2断熱層が硬化した後、該表面に慣用の釉薬
のスリツプを散布し乾燥する。次いで散布面以外
の面を断熱材で覆つた後、通常の方法で釉薬の溶
ける温度で加熱することにより、所望の施釉けい
酸カルシウム成形体が得られる。
尚、強度の大きい断熱層が必要な場合には、第
1断熱層上にメタルラス等を張り付けた上に前記
モルタル混練物を塗布するようにすれば効果的で
ある。
次に本発明を実施例によつて説明する。
ホ 実施例
実施例 1〜3
市販の軽量気泡コンクリート版(日本イトン工
業社製「イトン」を切断加工し60×60×10cmの大
きさの基材4枚を得た。又セメント、耐アルカリ
ガラス繊維、保水剤、パーライト及び水を第1表
に示す配合割合で混合し繊維質混合物を得た。
更に、早強ポルトランドセメント(日本セメン
ト社製「大日本早強セメント」)100重量部に対し
川砂(富士川産)160重量部、水50重量部、高性
能減水剤(花王社製「マイテイ150」)2重量部配
合混合しモルタル混練物を得た。
上記のようにして得た基材、繊維質混合物、及
びモルタル混練物を用いて下記の方法で3コの施
釉けい酸カルシウム成形体をつくつた。
まず、3枚の基材表面に水湿しを行なつた後、
直ちに3種類の繊維質混合物をそれぞれ別々に鏝
で押し付けながら厚さ5mmに塗布し、その上にモ
ルタル混練物を鏝で押し付けながら表面が平坦に
なるように厚さ5mm塗布した後24時間放置して硬
化させた。硬化後、硬化体の表面に、市販の釉薬
(日本琺瑯釉薬社製「LW−11a」)を水に分散さ
せたスリツプをスプレーで散布し乾燥させた。乾
燥後、散布面以外の面を無機繊維(イソライト工
業社製「カウオール」)で覆つた後、散布面が800
℃になるように15分間遠赤外線を照射して釉薬を
モルタル層に融着させ放冷した。
得られた施釉けい酸カルシウム各成形体の亀裂
発生状況を調べたところ、繊維質混合物層とモル
タル混練物層、基材と繊維混合物層及び基材自体
にも亀裂はなく、釉面も美麗に仕上がつていた。
比較例 1
水湿しを行なつた基材に、実施例で用いたモル
タル混練物を厚さ5mmに塗布し、以下実施例と同
様の手順に従つて施釉を行なつた。
得られた施釉けい酸カルシウム成形体について
亀裂発生状況を調べた結果、基材に多数の亀裂が
発生し、基材とモルタル間にも亀裂が発生してい
た。
B. Field of Industrial Application The present invention relates to a method for producing a glazed calcium silicate molded body. B. Prior Art Glazed calcium silicate molded bodies are attracting attention as building materials, such as exterior materials, because of their beautiful glazed surfaces and good durability. The method for producing a glazed calcium silicate molded object is to use a calcium silicate molded object as a base material (hereinafter simply referred to as "base material").
The method used was to seal the surface and then glaze it to eliminate pores.
However, this method heats the glazed surface when applying the glaze.
When the base material is subsequently cooled, shrinkage cracks occur between the heated portion of the surface layer of the base material and the unheated portion of the deeper layer because the shrinkage rate is different between the heated portion and the deeper unheated portion. On the other hand, based on conventional experience that cracks do not occur in cement mortar (hereinafter simply referred to as "mortar") when the surface is coated with glaze, a method applying this technology, that is, a method in which mortar is applied to the base material and then glazed, has been attempted. It was done. However, this method was not put into practical use because cracks occurred at the interface (adhesive surface) between the base material and mortar due to poor adhesion of the mortar to the base material. In this manner, none of the conventionally employed methods has been able to solve the problem of cracks occurring in the base material or the interface. Therefore, as a means of suppressing the occurrence of cracks, the applicant proposed a method of providing a heat insulating layer between the base material and the glazed layer, that is, applying a mixture of phosphate adhesive, pearlite, and water to the surface of the base material. We proposed a method for producing a glazed calcium silicate molded body, which is heated and hardened to form a heat insulating layer and then glazed (Japanese Patent Laid-Open No. 129566/1983). C. Problems to be Solved by the Invention The method for forming the heat insulating layer suppresses the occurrence of cracks and has achieved its purpose to some extent. However, this method requires
Two heating and cooling processes are required, one for curing the phosphate adhesive to form a heat insulating layer and the other for applying the glaze, and the repeated heating and cooling process makes the process that much more complicated. It also had the disadvantage of large energy loss. D. Means for Solving the Problem The present inventors have proposed that the heat insulating layer be formed at room temperature so that the heating and cooling process only needs to be performed once in the glazing process, and that there is a difference in composition between the base material and the glazed layer. The present invention was achieved based on the knowledge that a glazed calcium silicate molded article without cracking on the base material or interface can be obtained by forming two heat insulating layers and then applying glaze. That is, in the present invention, a mixture of a hydraulic substance, an inorganic fiber, a water retention agent, and water is applied to the surface of a calcium silicate molded body (base material) to form a first heat insulating layer, and then a mortar kneaded material is applied. The method for producing a glazed calcium silicate molded article is characterized in that the second heat insulating layer is formed, cured and dried, and then glazed. The reason for providing the first heat insulating layer in the present invention is to block the heat of the second heat insulating layer from being transmitted to the base material in the glazing process, to integrate the base material and the second heat insulating layer, and to allow thermal expansion of the first heat insulating layer. This is to provide a buffering effect that absorbs. The substrate used in the present invention refers to a molded body made of calcium silicate, such as lightweight aerated concrete (ALC). Examples of the hydraulic substance include Portland cement, mixed cement, and super fast-hardening cement. Inorganic fibers are blended to enhance insulation and buffering effects, such as alkali-resistant glass fibers,
Examples include artificial or natural inorganic fibers such as carbon fiber, alumina fiber, steel fiber, and asbestos. Water retention agents are added to prevent water from being absorbed into the substrate when a fibrous mixture is applied to the surface of the substrate. ), polyvinyl alcohol (PVA), polyethylene oxide (PEO),
Examples include polyacrylamide (PAA). In addition to the above formulations, for example, when applying a glaze with a high melting point glaze or when it is necessary to reduce the thickness of the heat insulating layer, it is necessary to use a lightweight bone that does not impair adhesion to the base material. Material (e.g. perlite)
There is no problem in blending. Next, the blending ratio of the raw materials for forming the heat insulating layer will be explained. The inorganic fiber is preferably blended in an amount of 0.5 to 5.0 vol% of the total volume of the mixture mixed for the first heat insulating layer. If it is less than 0.5 vol%, the insulation effect and buffering effect will be small, and if it exceeds 5.0 vol%, the fibers will be difficult to disperse and uniform mixing will be difficult. The water retention agent is blended in an amount of 0.05 to 5.0 wt% with respect to the hydraulic substance. If it is less than 0.05 wt%, the water retention effect will be weak and water will be absorbed into the base material, which is not preferable. If it exceeds 5.0 wt%, it inhibits the hydration reaction of the hydraulic substance, which is not preferable. Water may be added to the extent that the mixture is soft enough to be applied, and as a guideline, the amount of water is 50 to 300 wt% based on the hydraulic substance. If it is less than 50 wt%, the fibrous mixture will be hard and difficult to apply to the substrate, and if it exceeds 300 wt%, the fluidity will be too high and it will be difficult to apply it to a predetermined thickness. The reason for providing the second heat insulating layer is that if the glaze is applied directly to the surface of the first heat insulating layer, the fibers exposed on the surface of the first heat insulating layer may change color during heating, resulting in an unintended pattern on the glazed surface, or if the glazed surface is too exposed. This is to prevent unsightly patterns from forming and to improve surface strength. The hydraulic material used for the second heat insulating layer is the first heat insulating layer.
It is the same as that used in the insulation layer. Commercially available artificial or natural sand is used.
The mixing ratio of sand and hydraulic substance is the same as that of normal mortar for plastering, and the ratio of sand to hydraulic substance is 60~
300wt% is preferred. If it is less than 60wt%, it will become a rich mortar, which will shrink more when hardened and cause minute cracks, which is undesirable.On the other hand, if it exceeds 300wt%, the water-cement ratio will become too large and the strength will decrease. This is not desirable. The amount of water blended is such that the mixture is soft enough to be applied, and is generally 30 to 70 wt% based on the hydraulic material.
If it is less than 30wt%, the mixture will not be uniform and it will be difficult to apply it. If it exceeds 70 wt%, the fluidity of the kneaded product becomes too high, making coating work difficult, and both are unfavorable. In order to ensure the strength of the molded article, it is preferable to reduce the amount of water and the number of air bubbles as much as possible, so there is no problem in adding a water reducing agent or an antifoaming agent as appropriate. The thickness of the first and second heat insulating layers may be set to the required thickness of the glazed base material, but at least in order to prevent the base material from cracking due to heating in the glazing process, Preferably, each heat insulating layer has a thickness of 3 to 10 mm. Next, a method for manufacturing a glazed calcium silicate molded body of the present invention will be explained. After applying the fibrous mixture for the first heat insulating layer to a predetermined thickness by sufficiently pressing it with a trowel on the surface of the base material that has been processed to the required dimensions, apply the mortar mixture for the second heat insulating layer to the surface with a trowel. Apply it evenly to a predetermined thickness without forming bubbles and cure. After the second insulation layer has hardened, the surface is sprinkled with a conventional glaze slip and allowed to dry. Next, after covering the surfaces other than the sprayed surface with a heat insulating material, the desired glazed calcium silicate molded body is obtained by heating in a conventional manner at a temperature at which the glaze melts. If a high-strength heat insulating layer is required, it is effective to apply the mortar mixture on top of a metal lath or the like on the first heat insulating layer. Next, the present invention will be explained with reference to examples. Examples Examples 1 to 3 Commercially available lightweight aerated concrete slabs ("Iton" manufactured by Nippon Iton Kogyo Co., Ltd.) were cut to obtain 4 base materials with a size of 60 x 60 x 10 cm. Also, cement and alkali-resistant glass were obtained. A fibrous mixture was obtained by mixing fibers, a water retention agent, perlite, and water in the proportions shown in Table 1.Furthermore, for 100 parts by weight of early strength Portland cement ("Dainippon Early Strength Cement" manufactured by Nippon Cement Co., Ltd.) A mortar mixture was obtained by mixing 160 parts by weight of river sand (produced in Fujikawa), 50 parts by weight of water, and 2 parts by weight of a high-performance water reducer ("Mighty 150" manufactured by Kao Corporation).The base material obtained as described above, Three glazed calcium silicate molded bodies were made using the fibrous mixture and the mortar mixture in the following manner. First, after moistening the surfaces of the three base materials,
Immediately, each of the three types of fibrous mixture was applied separately to a thickness of 5 mm by pressing with a trowel, and on top of that, the mortar mixture was applied to a thickness of 5 mm by pressing with a trowel so that the surface was flat, and then left for 24 hours. and cured. After curing, a slip prepared by dispersing a commercially available glaze ("LW-11a" manufactured by Nippon Horo Glaze Co., Ltd.) in water was sprayed onto the surface of the cured product and dried. After drying, cover the surface other than the sprayed surface with inorganic fiber ("Cow All" manufactured by Isolite Industries Co., Ltd.), and then
The glaze was fused to the mortar layer by irradiation with far infrared rays for 15 minutes so that the temperature reached ℃, and then allowed to cool. When we investigated the occurrence of cracks in each of the obtained glazed calcium silicate moldings, we found that there were no cracks in the fibrous mixture layer, mortar mixture layer, base material, fiber mixture layer, or base material itself, and the glazed surface was beautiful. It was finished. Comparative Example 1 The mortar kneaded material used in the examples was applied to a thickness of 5 mm on a substrate that had been moistened with water, and glaze was applied in accordance with the same procedure as in the examples. As a result of examining the occurrence of cracks in the obtained glazed calcium silicate molded article, it was found that many cracks had occurred in the base material, and cracks had also occurred between the base material and the mortar.
【表】【table】
【表】
ヘ 発明の効果
従来、施釉けい酸カルシウム成形体の製造にお
いては、基材にリン酸塩系接着剤を塗布して加熱
し、更に施釉する際にも加熱していた。
このように加熱工程が2度あること自体、工程
を複雑にするばかりでなく、加熱によつて亀裂を
発生させ易いという欠点があつたが、本発明の方
法は断熱層形成に加熱を要さない水硬性物質を採
用したことにより、加熱工程が1回で済み、工程
が簡素化されるばかりでなく、施釉けい酸カルシ
ウム成形体の基材や断熱層に亀裂が発生すること
もなく、施釉面も美麗に仕上げることができる。[Table] F. Effects of the Invention Conventionally, in the production of glazed calcium silicate molded bodies, a phosphate adhesive was applied to a base material and heated, and further heating was applied when applying the glaze. The fact that the heating process is performed twice in itself not only complicates the process, but also has the disadvantage that cracks are likely to occur due to heating, but the method of the present invention does not require heating to form a heat insulating layer. By using a non-hydraulic material, only one heating process is required, which not only simplifies the process, but also eliminates the occurrence of cracks in the base material and heat insulation layer of the glazed calcium silicate molded body. The surface can also be beautifully finished.
Claims (1)
無機繊維、保水剤及び水を混合した混合物を塗布
した後、モルタル混練物を塗布し硬化乾燥させて
から施釉することを特徴とする施釉けい酸カルシ
ウム成形体の製造方法。1 Hydraulic substance on the surface of the calcium silicate molded body,
A method for producing a glazed calcium silicate molded body, which comprises applying a mixture of inorganic fibers, a water retention agent, and water, then applying a mortar mixture, hardening and drying, and then applying a glaze.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP23800286A JPS6395181A (en) | 1986-10-08 | 1986-10-08 | Manufacture of glazed calcium silicate formed body |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP23800286A JPS6395181A (en) | 1986-10-08 | 1986-10-08 | Manufacture of glazed calcium silicate formed body |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6395181A JPS6395181A (en) | 1988-04-26 |
| JPH032831B2 true JPH032831B2 (en) | 1991-01-17 |
Family
ID=17023672
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP23800286A Granted JPS6395181A (en) | 1986-10-08 | 1986-10-08 | Manufacture of glazed calcium silicate formed body |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6395181A (en) |
-
1986
- 1986-10-08 JP JP23800286A patent/JPS6395181A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6395181A (en) | 1988-04-26 |
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