JPH03266639A - Ceramic sheet with moisture adjusting functionality - Google Patents
Ceramic sheet with moisture adjusting functionalityInfo
- Publication number
- JPH03266639A JPH03266639A JP2067460A JP6746090A JPH03266639A JP H03266639 A JPH03266639 A JP H03266639A JP 2067460 A JP2067460 A JP 2067460A JP 6746090 A JP6746090 A JP 6746090A JP H03266639 A JPH03266639 A JP H03266639A
- Authority
- JP
- Japan
- Prior art keywords
- raw material
- base layer
- layer
- humidity control
- decorative layer
- 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
Links
- 239000000919 ceramic Substances 0.000 title claims abstract description 51
- 239000008187 granular material Substances 0.000 claims abstract description 40
- 239000002994 raw material Substances 0.000 claims abstract description 38
- 239000000835 fiber Substances 0.000 claims abstract description 17
- 238000005187 foaming Methods 0.000 claims abstract description 13
- 239000002245 particle Substances 0.000 claims abstract description 13
- 239000002002 slurry Substances 0.000 claims abstract description 12
- 238000010438 heat treatment Methods 0.000 claims abstract description 8
- 239000011148 porous material Substances 0.000 claims description 11
- 238000010304 firing Methods 0.000 claims description 7
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 5
- 239000004113 Sepiolite Substances 0.000 claims description 3
- 229910052624 sepiolite Inorganic materials 0.000 claims description 3
- 235000019355 sepiolite Nutrition 0.000 claims description 3
- 229910021536 Zeolite Inorganic materials 0.000 claims description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims description 2
- 239000010457 zeolite Substances 0.000 claims description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 abstract description 17
- 239000000843 powder Substances 0.000 abstract description 12
- 239000000463 material Substances 0.000 abstract description 8
- 235000017550 sodium carbonate Nutrition 0.000 abstract description 8
- 229910000029 sodium carbonate Inorganic materials 0.000 abstract description 8
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 abstract description 8
- 239000011521 glass Substances 0.000 abstract description 7
- 239000010433 feldspar Substances 0.000 abstract description 5
- 239000010459 dolomite Substances 0.000 abstract description 4
- 229910000514 dolomite Inorganic materials 0.000 abstract description 4
- 239000004317 sodium nitrate Substances 0.000 abstract description 4
- 235000010344 sodium nitrate Nutrition 0.000 abstract description 4
- 235000019738 Limestone Nutrition 0.000 abstract description 3
- 239000006028 limestone Substances 0.000 abstract description 3
- 239000000203 mixture Substances 0.000 abstract description 3
- 239000002253 acid Substances 0.000 abstract description 2
- 239000004927 clay Substances 0.000 abstract description 2
- 239000004088 foaming agent Substances 0.000 abstract description 2
- 238000010030 laminating Methods 0.000 abstract description 2
- 239000004575 stone Substances 0.000 abstract description 2
- 238000001354 calcination Methods 0.000 abstract 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract 1
- 230000009970 fire resistant effect Effects 0.000 abstract 1
- 239000000155 melt Substances 0.000 abstract 1
- 230000008018 melting Effects 0.000 abstract 1
- 238000002844 melting Methods 0.000 abstract 1
- 239000011701 zinc Substances 0.000 abstract 1
- 229910052725 zinc Inorganic materials 0.000 abstract 1
- 235000016804 zinc Nutrition 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 67
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 7
- 239000010440 gypsum Substances 0.000 description 5
- 229910052602 gypsum Inorganic materials 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 238000010521 absorption reaction Methods 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 241000218645 Cedrus Species 0.000 description 3
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 239000006260 foam Substances 0.000 description 3
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 3
- 235000019353 potassium silicate Nutrition 0.000 description 3
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- 229910052845 zircon Inorganic materials 0.000 description 3
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000011449 brick Substances 0.000 description 2
- 239000004566 building material Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000004891 communication Methods 0.000 description 2
- 239000004567 concrete Substances 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- -1 earth Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 238000011049 filling Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 230000029058 respiratory gaseous exchange Effects 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- 235000014692 zinc oxide Nutrition 0.000 description 2
- 241001131796 Botaurus stellaris Species 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 235000017284 Pometia pinnata Nutrition 0.000 description 1
- 240000007653 Pometia tomentosa Species 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 235000010338 boric acid Nutrition 0.000 description 1
- 239000007931 coated granule Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000003795 desorption Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 230000014509 gene expression Effects 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 235000013379 molasses Nutrition 0.000 description 1
- 239000010451 perlite Substances 0.000 description 1
- 235000019362 perlite Nutrition 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 229940072033 potash Drugs 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000001360 synchronised effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000010257 thawing Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Landscapes
- Building Environments (AREA)
- Finishing Walls (AREA)
- Laminated Bodies (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野]
本発明は調湿機能を有するセラミック板に関する。さら
に詳しくは、軽量大型板であり、調湿部分の強度が改善
された調湿機能を有するセラミック板に関する。本発明
にお(・て調湿機能とは、吸湿機能および放湿機能を意
味し、たとえば本発明のセラミック板を壁材として用い
たばあいに、室内が高湿度のときは壁材か湿気を吸収し
、逆に室内が低湿度のときは壁材が湿気を室内に放出す
るような機能のことをいう。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a ceramic plate having a humidity control function. More specifically, the present invention relates to a ceramic plate that is a large, lightweight plate and has a humidity control function with improved strength in the humidity control portion. In the present invention, the term "humidity control function" refers to a moisture absorption function and a moisture release function. For example, when the ceramic board of the present invention is used as a wall material, when the indoor humidity is high, the wall material This refers to the function of the wall material to absorb moisture and, conversely, to release moisture into the room when the humidity is low.
[従来の技術および発明が解決しようとする課題]
従来の日本の建物は、主として木、土および紙によって
構成されており、屋外の気候に影響され易いものの、構
造物のすべてが呼吸作用をなしており、高湿度のときは
水分を吸収し、逆に乾燥時には水分を放出して屋内の湿
度調整を行っていた。[Prior art and problems to be solved by the invention] Traditional Japanese buildings were mainly constructed of wood, earth, and paper, and although they were easily affected by the outdoor climate, all of the structures had a breathing effect. When the humidity is high, it absorbs moisture, and when it is dry, it releases moisture to adjust indoor humidity.
ところが、昨今の建物はコンクリート構造に代表される
ように密閉型のものが多く、通気性、呼吸作用のない構
造となっている。したがって、湿度の高い地方ではとく
に結露による弊害が大きく、建物の居住性を低下させて
いた。However, many buildings these days are of a closed type, as typified by concrete structures, and have a structure that does not allow ventilation or breathing. Therefore, in regions with high humidity, condensation is particularly harmful, reducing the livability of buildings.
このため、従来にあっては、石膏ボードに化粧紙を貼る
とか、コンクリートの表面に吸湿シートを貼るなどして
居住性を保ってきたが、石膏ボードは水に弱く、また装
飾性や強度に劣るという問題があり、吸湿シートは汚れ
易く取り替えが必要であるという問題がある。したがっ
て、タイルのようなセラミック板であって、しかも調湿
機能を有する建材が久しく望まれていた。For this reason, in the past, livability was maintained by pasting decorative paper on gypsum board or moisture-absorbing sheets on concrete surfaces, but gypsum board is vulnerable to water and has poor decorative and strength properties. There is a problem that the moisture absorption sheet is inferior, and that the moisture absorbing sheet gets dirty easily and needs to be replaced. Therefore, there has long been a desire for a building material that is a ceramic plate like a tile and has a humidity control function.
そこで、かかる建材をうるべく鋭意研究を重ねた結果、
本発明者らは、発泡性無機質原料を加熱発泡せしめた基
層と化粧層とのあいだに調湿無機原料を含む調湿層を介
在せしめたセラミック板が調湿機能を有する一方で優れ
た断熱性や耐火性を有することを見出し、さきに3件の
特許出願を行った(特願昭62−271407号、特願
昭62−271408号および特願昭62−27140
9号)。Therefore, as a result of intensive research into such building materials,
The present inventors have discovered that a ceramic plate in which a humidity control layer containing a humidity control inorganic raw material is interposed between a base layer formed by heating and foaming a foamable inorganic raw material and a decorative layer has a humidity control function and an excellent heat insulation property. He discovered that it has fire resistance and fire resistance, and filed three patent applications (Japanese Patent Application No. 62-271407, Japanese Patent Application No. 62-271408, and Japanese Patent Application No. 62-27140).
No. 9).
しかし、調湿原料を乾式粉砕し粒径1〜2mlに造粒し
たものと基層用または化粧層用造粒物との混合物を調湿
層の原料にしたり(特願昭62−271407号)、格
子状の発泡体と格子の開口部内に充填された調湿原料と
で調湿層を構成するばあい(特願昭62−271408
号)、えられたセラミック板の調湿機能は充分であるが
、大板を切断したときに切口より調湿機能を有する造粒
物がこぼれ落ちたり、切口にあられれた調湿部分の強度
が小さいという問題があった。これは、調湿機能粒が造
粒物であり、微粒子の結合力か弱いためであり、またこ
ほれ落ちるのは調湿機能粒は焼成しても溶着せず造粒物
同士の結合かえられないからである。However, a mixture of dry-pulverized humidity control raw materials and granules to a particle size of 1 to 2 ml and granules for the base layer or decorative layer is used as the raw material for the humidity control layer (Japanese Patent Application No. 62-271407). In the case where the humidity control layer is composed of a lattice-shaped foam and a humidity control raw material filled in the openings of the lattice (Japanese Patent Application No. 62-271408
The humidity control function of the obtained ceramic plate is sufficient, but when cutting a large plate, the granules that have a humidity control function may fall out from the cut, and the strength of the humidity control part that is formed on the cut may be reduced. The problem was that it was small. This is because the moisture control function granules are granules, and the bonding strength of the fine particles is weak.Also, the reason why the moisture control function granules break down is that even when fired, the moisture control function granules do not weld and the bond between the granules cannot be changed. It is from.
また、調湿原料を抄造法によりシート状にして埋設して
もwi湿機能を有するが、この抄造シートを基板層と化
粧層のあいだに介在せしめて、これらを溶着一体化する
にはシートに孔径4〜5厘膳の孔をあけ、この孔で化粧
原料と基板原料を接触溶着させ、溶着しない調湿シート
を保持しなければならない。こうして、シートの孔あけ
の工程が必要になるとともに約30%の孔部分の原料ロ
スを生じ、製造コストを押し上げる要因となっていた。Furthermore, even if the humidity control raw material is made into a sheet by a paper-forming method and buried, it still has a moisture function, but in order to interpose this paper-made sheet between the substrate layer and the decorative layer and integrate them by welding, it is necessary to A hole with a diameter of 4 to 5 mm must be made, the cosmetic raw material and the substrate raw material must be contacted and welded through the hole, and the humidity control sheet that is not welded must be held. In this way, a step of punching holes in the sheet becomes necessary, and about 30% of raw material is lost in the holes, which causes an increase in manufacturing costs.
本発明は、斜上の事情に鑑み、前記従来技術の有する欠
点が解消されたセラミック板を提供することを目的とす
る。すなわち、本発明の目的は、切断箇所より調湿原料
がこぼれ落ちたり、化粧層が剥離することのない、調湿
機能を有するセラミック板を提供することである。SUMMARY OF THE INVENTION In view of the above-mentioned problem, the present invention aims to provide a ceramic plate that eliminates the drawbacks of the prior art. That is, an object of the present invention is to provide a ceramic plate having a humidity control function that prevents humidity control raw materials from spilling from the cut portions and prevents the decorative layer from peeling off.
[課題を解決するための手段]
本発明の調湿機能を有するセラミック板は、発泡性無機
質造粒物を加熱発泡せしめた独立気孔性の基層と、該基
層上に形成された、調湿原料を含む網目状セラミックシ
ートと、該セラミックシートの上に形成され、発泡性無
機質造粒物を加熱発泡せしめた連通気孔性の化粧層とか
らなり、前記基層、セラミックシートおよび化粧層が焼
成により溶化一体化されてなることを特徴としている。[Means for Solving the Problems] The ceramic plate having a humidity control function of the present invention includes a closed pore base layer formed by heating and foaming an expandable inorganic granule, and a humidity control raw material formed on the base layer. The base layer, the ceramic sheet, and the decorative layer are solvated by firing. It is characterized by being integrated.
[実施例]
以下、添付した図面に基づき本発明のセラミック板を説
明する。[Example] Hereinafter, the ceramic plate of the present invention will be explained based on the attached drawings.
独立気孔性の基層(1)は、酸性白土、抗火石、シラス
、真珠岩などを主原料として、これにソーダ灰、ガラス
粉、硝酸ソーダ、硼酸、硼砂、水ガラスなどの媒溶材や
、ドロマイト、S]C。The independent porosity base layer (1) is mainly made of acid clay, anti-firestone, shirasu, perlite, etc., and contains solvents such as soda ash, glass powder, sodium nitrate, boric acid, borax, water glass, etc., and dolomite. ,S]C.
炭酸カリウム、炭酸ソーダなどの発泡剤などを補助的に
配合して325メツシュバス96%以上程度に乾式粉砕
した原料を、たとえばパン型造粒機を用いて粒径1〜2
.51程度に造粒したものを加熱発泡せしめた層である
。造粒物は造粒したのちに乾燥して用いられる。The raw material is dry-pulverized to about 96% or more of 325 mesh bath with supplementary foaming agents such as potassium carbonate and soda carbonate, and is then reduced to a particle size of 1 to 2 using a pan-type granulator, for example.
.. This layer is made by heating and foaming granules that have been granulated to about 51 mm. The granulated product is used after being granulated and then dried.
基層(1)の内部にはセラミック板の強度を保持するた
めにラス網などの補強材を埋設しておくのが好ましい。It is preferable to embed a reinforcing material such as a lath net inside the base layer (1) in order to maintain the strength of the ceramic plate.
基層(1)の厚さは本発明においてとくに限定されない
が、概ね15〜25svが目安である。The thickness of the base layer (1) is not particularly limited in the present invention, but is approximately 15 to 25 sv.
(2)は前記基層(1)上に載置された網目状のセラミ
ックシートである。該シート(2)はたとえば線径が0
.5■■で孔径が5〜10mmの有機質繊維ネット(3
)に後述する泥漿状の調湿原料を付着せしめたものであ
る。シート(2)は、まず繊維ネット(3)をPVAや
CMCなどの糊剤を入れた塩化マグネシームの7%溶液
やカリ水ガラスの10%溶液などに浸して乾燥させ、つ
いで乾燥後の繊維ネット(3)を活性アルミナにバイン
ダーとしてセピオライトやゼオライトを加配して湿式粉
砕した泥漿中に浸漬したり、また繊維ネット(3)に前
記泥漿をかけ流しすることでえられる。繊維ネット(3
)を前記泥漿中に浸漬すると泥漿はネット(3)を構成
する繊維にからまり、付着する。モして泥漿の付着によ
り繊維ネット(3)の網目の開口部は小さくなるが、こ
の状態で発泡性無機質造粒物が該開口部を通過できるよ
うに繊維ネットを選定する必要がある。活性アルミナを
配合した調湿原料は、焼成により固化して型を保つが、
溶化して基層または化粧層と一体化しないので、セラミ
ックシートの上にチャージされる化粧層用造粒物または
該シートにある基層用造粒物が繊維ネットの網目を通っ
て基層用造粒物または化粧層用造粒物と溶化一体化して
活性アルミナを含むネットを包むようにして保持せしめ
るためである。したがって、網目の大きさは造粒された
化粧層用または基層用造粒物がそれぞれ基層用または化
粧層用造粒物とより多く接触できるよう選定する必要が
ある。具体的に言えば、粒径1〜2.511m程度の化
粧層用造粒物を用いるばあいは、繊維ネットへの泥漿の
付着を考慮して、5〜IOam程度の開口部を有する繊
維ネットを選定する必要かある。(2) is a reticulated ceramic sheet placed on the base layer (1). The sheet (2) has a wire diameter of 0, for example.
.. Organic fiber net (3
) to which a slurry-like humidity control material, which will be described later, is attached. The sheet (2) is made by first soaking the fiber net (3) in a 7% solution of magnesium chloride or a 10% solution of potash water glass containing a sizing agent such as PVA or CMC, and then drying it. It can be obtained by immersing (3) in a wet-pulverized slurry of activated alumina with the addition of sepiolite or zeolite as a binder, or by pouring the slurry over a fiber net (3). Fiber net (3
) is immersed in the slurry, the slurry becomes entangled with and adheres to the fibers constituting the net (3). Although the openings of the fiber net (3) become smaller due to the adhesion of the slurry, it is necessary to select the fiber net so that the expandable inorganic granules can pass through the openings in this state. Humidity control raw materials containing activated alumina solidify and retain their shape through firing, but
Since it is not dissolved and integrated with the base layer or decorative layer, the granules for the decorative layer charged on the ceramic sheet or the granules for the base layer on the sheet pass through the mesh of the fiber net and become the granules for the base layer. Alternatively, it is solubilized and integrated with the granules for the decorative layer to wrap and hold the net containing activated alumina. Therefore, the size of the mesh needs to be selected so that the granulated granules for the decorative layer or the base layer can come into contact with the granules for the base layer or the decorative layer as much as possible. Specifically, when using granules for the decorative layer with a particle size of about 1 to 2.511 m, a fiber net with openings of about 5 to IOam is used, taking into account the adhesion of slurry to the fiber net. Is it necessary to select
セラミックシート(2)の厚さは本発明においてとくに
限定されないが、概ね2〜4mmが目安である。Although the thickness of the ceramic sheet (2) is not particularly limited in the present invention, it is generally 2 to 4 mm.
連通気孔性の化粧層(4)用原料としては、長石、ソー
ダ灰、硝酸ソーダ、ドロマイト、ジルコニット、亜鉛華
、石灰石、ガラス粉、ジルコンフリットなどを適宜組み
合せた配合原料を用いることができる。このような組み
合せの例としては、長石、ソーダ灰、ジルコニット、亜
鉛華、石灰石およびジルコンフリットからなる組み合せ
や、長石、ソーダ灰、ジルコニット、ジルコンフリット
およびガラス粉からなる組み合せなどがある。かかる原
料を乾式粉砕し、そののちパン型造粒機にて0.5〜1
.5ms程度に造粒したものを用いることができる。As raw materials for the open-pored decorative layer (4), blended raw materials in which feldspar, soda ash, sodium nitrate, dolomite, zirconite, zinc white, limestone, glass powder, zircon frit, etc. are appropriately combined can be used. Examples of such combinations include combinations of feldspar, soda ash, zirconite, zinc white, limestone, and zircon frit, and combinations of feldspar, soda ash, zirconite, zircon frit, and glass powder. The raw materials are dry-pulverized and then used in a pan-type granulator to give a powder of 0.5 to 1
.. Particles granulated to about 5 ms can be used.
化粧層用造粒物は、粒と粒の接触点で溶化結合するかガ
ラス化して粒界を埋めてしまったり、充分発泡しすぎて
粒界のすべてを埋めてしまわないような配合とする必要
がある。具体的には、発泡率を小さくすることで発泡後
に連通気孔を残すことかできる。すなわち、発泡率が小
さいばあい、加熱により溶化発泡した各校は点接着で層
を形成し、粒と粒との粒界は気孔を残している。発泡率
が大きいばあいは、粒の体積増と圧力により粒界は潰さ
れて連通気孔は無くなるが、発泡率が小さいときは発泡
後に連通気孔が残るのである。この化粧層に残されてい
る連通気孔を通って湿気もしくは湿分はセラミックシー
ト内の調湿原料に吸着され、また屋内湿度が低下したと
きは調湿原料より排出される湿気はこの連通気孔を通っ
て屋内に排出される。このようにして、室内は常に快適
な湿度状態にコントロールされるのである。Granules for the decorative layer need to be formulated in such a way that they do not melt and bond or vitrify at the point of contact between grains, filling the grain boundaries, or foaming too much to fill all the grain boundaries. There is. Specifically, by reducing the foaming rate, continuous pores can be left after foaming. That is, when the foaming rate is small, the particles melted and foamed by heating form a layer by point adhesion, leaving pores at the grain boundaries between the grains. When the foaming rate is high, the grain boundaries are crushed by the increased grain volume and pressure, and continuous pores disappear, but when the foaming rate is low, continuous pores remain after foaming. Moisture or moisture passes through the communication holes left in this decorative layer and is adsorbed by the humidity control material in the ceramic sheet, and when the indoor humidity decreases, the moisture discharged from the humidity control material passes through the communication holes. and is discharged indoors. In this way, the indoor humidity is always controlled to a comfortable level.
化粧層は、自由に色付けができるように基本配合が白く
なるように調整するのが好ましく、またロール抑圧によ
りレリーフ模様も施せるように軟化するのが好ましい。The basic composition of the decorative layer is preferably adjusted so that it is white so that it can be colored freely, and it is also preferably softened so that a relief pattern can be applied by rolling.
化粧層(4]表面のデザインは、ピグメントにより自由
に着色できるとともに、着色粒の混合、光沢の調整、溶
化の程度により様々な表情を与えることができるが、い
ずれのばあいであっても常に粒界を埋めることなく連通
気孔を保持することが大切である。The design of the surface of the makeup layer (4) can be freely colored with pigments, and various expressions can be given by mixing the colored particles, adjusting the gloss, and the degree of solubilization, but in any case, it is always It is important to maintain continuous pores without filling grain boundaries.
化粧層の厚さも基層など他の層間様にとくに限定される
ものではないが、概ね3〜5II1mが目安である。The thickness of the decorative layer is not particularly limited to the thickness of other interlayers such as the base layer, but it is generally 3 to 5 II 1 m as a guide.
本発明のセラミック板では、連続したネット状セラミッ
クシートに湿式粉砕して泥漿状になった調湿原料を付着
させており、このため調湿原料粒子は相互に強く結合し
ている。したかって、セラミック板の切断による調湿原
料のこぼれ落ちもなくなり、切断の調湿層(セラミック
シート)の強度を為めることも可能となる。In the ceramic plate of the present invention, a wet-pulverized humidity control raw material in the form of a slurry is attached to a continuous net-like ceramic sheet, so that the humidity control raw material particles are strongly bonded to each other. Therefore, the humidity control raw material does not spill out when the ceramic plate is cut, and the strength of the cut humidity control layer (ceramic sheet) can be increased.
本発明のセラミック板は、前述した基層用造粒物を耐熱
メツシュベルトなどの上に層状に載置し、その上にセラ
ミックシートおよび化粧層用造粒物をこの順序で積層し
、えられた積層体をトンネルキルンやローラーハースキ
ルンなどの焼成炉中に搬入して、加熱焼成して一体化せ
しめることで製造される。The ceramic plate of the present invention is produced by placing the above-mentioned base layer granules in a layered manner on a heat-resistant mesh belt or the like, and then laminating the ceramic sheet and the decorative layer granules in this order. It is manufactured by transporting the body into a firing furnace such as a tunnel kiln or roller hearth kiln, and heating and firing it to make it into one piece.
つぎに実施例に基づき本発明のセラミック板を説明する
が、本発明はもとよりかかる実施例にのみ限定されるも
のではない。Next, the ceramic plate of the present invention will be explained based on Examples, but the present invention is not limited to these Examples.
実施例1
基層用造粒物の調整
大谷石6445%(重量%、以下同様)、水ガラス粉5
%、ソーダ灰18%、王立タルク12%およびSiC0
,5%からなる配合原料を10mmのスチールボールと
ともにボールミルに入れ5時間のあいだ乾式粉砕した。Example 1 Preparation of granules for base layer Oya stone 6445% (weight %, same hereinafter), water glass powder 5
%, soda ash 18%, royal talc 12% and SiC0
, 5% was placed in a ball mill with 10 mm steel balls and dry ground for 5 hours.
えられた粉末は325メツシュパス96%以上の大きさ
であった。The resulting powder had a size greater than 96% of the 325 mesh pass.
この粉末にバインダー液(糖蜜15%水溶液)を噴霧し
ながらパン型造粒機にて造粒し、粒径1〜2.5■の造
粒物をえた。二〇造粒物をバイブリフト転勤温風乾燥機
にて造粒含水率3%以下となるように乾燥した。This powder was granulated using a pan-type granulator while spraying a binder liquid (molasses 15% aqueous solution) to obtain granules having a particle size of 1 to 2.5 square meters. 20 The granulated product was dried in a viblift transfer hot air dryer so that the moisture content of the granules was 3% or less.
セラミックシートの調製
目開き10m1X 6 mm、線径0.5■の繊維ネッ
ト(金山レース銖製のジャンボネット(商品名))の角
シート(100cmx 100C!りを水3gに苦汁8
90およびGL−05(商品名。日本合成■製PV^)
49iiを配合した溶液に浸して乾燥させた。Preparation of ceramic sheet A square sheet (100cm x 100C!) of fiber net (Jumbo Net (trade name) manufactured by Kanayama Lace) with an opening of 10m x 6mm and a wire diameter of 0.5cm is added to 3g of water and 8 pieces of bittern.
90 and GL-05 (product name. Nippon Gosei PV^)
It was soaked in a solution containing 49ii and dried.
一方、C−303(商品名。住友化学■製乾燥水酸化ア
ルミニウム)60重量部およびC−31(商品名。On the other hand, 60 parts by weight of C-303 (trade name, dried aluminum hydroxide manufactured by Sumitomo Chemical ■) and C-31 (trade name).
住友化学■製乾燥水酸化アルミニウム)20重量部から
なる水酸化アルミニウム80重量部、セピオライト20
重量部、解コウ剤(ポイズ530)0.7重量部、水6
0重量部からなる配合原料を磁器ボールとともにポット
ミルに入れて2時間湿式粉砕して泥漿状調湿原料をえた
。80 parts by weight of aluminum hydroxide, 20 parts by weight of dried aluminum hydroxide manufactured by Sumitomo Chemical ■, and 20 parts by weight of sepiolite.
Parts by weight, 0.7 parts by weight of defrosting agent (Poise 530), 6 parts by weight of water
A blended raw material containing 0 parts by weight was placed in a pot mill together with porcelain balls and wet-pulverized for 2 hours to obtain a slurry-like humidity control raw material.
この泥漿状調湿原料中に前記繊維ネットを浸漬させて、
該ネットに調湿原料を付着させた。The fiber net is immersed in this slurry-like humidity control raw material,
A humidity control raw material was attached to the net.
化粧層用造粒物の調製
長石粉54%、ガラス20%、ソーダ灰14%、硝酸ソ
ーダ296、ドロマイト3%およびジルコニット796
からなる配合原料をl Dmmのスチールボールととも
にポットミルに入れ3時間乾式粉砕した。えられた粉末
は325メツシュバス9696以上の大きさであった。Preparation of granules for decorative layer 54% feldspar powder, 20% glass, 14% soda ash, 296% sodium nitrate, 3% dolomite and 796 zirconite
The mixed raw material consisting of the following was put into a pot mill together with 1 Dmm steel balls and dry-milled for 3 hours. The powder obtained had a size of more than 325 mesh baths and 9696 mesh baths.
この粉末にバインダー液(モナードガム0.5%溶液)
を噴霧しながらパン型造粒機にて造粒し粒径0.5〜1
、0+++ll1O造粒物をえた。造粒物の含水率は
15%であった。二〇造粒物をパイプリフト転勤温風乾
燥機にて造粒物含水率3%以下となるように乾燥させた
。Add binder liquid (monard gum 0.5% solution) to this powder.
is granulated using a pan-type granulator while spraying to obtain a particle size of 0.5 to 1.
, 0+++ll1O granules were obtained. The moisture content of the granules was 15%. 20 The granulated material was dried in a pipe lift rotating hot air dryer so that the moisture content of the granulated material was 3% or less.
全長89mのトンネル炉内に架設された中1mの搬送用
耐熱メツシュベルト上に離型材としてアルミナを塗布し
、その上に予め用意しておいた基層用造粒物を厚さ8G
I11の層を形成するようにチャージした。その際、メ
ツシュベルトの速度に同調させたラス網をメンシュベル
ト−L51II11の位置に挿入しながら埋設した。Alumina was applied as a mold release material onto a medium 1m heat-resistant mesh belt for conveyance built in a tunnel furnace with a total length of 89m, and the base layer granules prepared in advance were coated on top of it to a thickness of 8G.
It was charged to form a layer of I11. At that time, a lath mesh synchronized with the speed of the mesh belt was inserted and buried at the position of the mesh belt L51II11.
ついで、準備しておいたセラミックシートを基層用造粒
物の上に置き、続いて該シートの上に化粧層用造粒物の
入ったホッパーの開口部を開き、厚さ4■の層を形成す
るよう自動チャージした。えられた積層体を20cm/
分の速度で予熱帯へ移送し、最高温度870°Cの焼成
帯、急冷帯、徐冷帯および冷却帯を通過せしめて焼成を
終了した。搬入から搬出までの所要時間は約200分で
あった。Next, the prepared ceramic sheet was placed on top of the granules for the base layer, and then the opening of the hopper containing the granules for the decorative layer was opened on top of the sheet, and a layer of 4 cm thick was placed on top of the sheet. It was automatically charged to form. The obtained laminate is 20cm/
The sample was transferred to a preheating zone at a speed of 1 minute, and passed through a firing zone with a maximum temperature of 870°C, a rapid cooling zone, a gradual cooling zone, and a cooling zone to complete firing. The time required from loading to unloading was approximately 200 minutes.
えられたセラミック板をr190cm、長さ100CO
Iの大きさに切断したか、基層は独立気孔である小孔の
揃った発泡体であり、その上に白色の調湿層があった。The obtained ceramic plate is r190cm, length 100CO
The base layer was a foam with closed pores, and there was a white humidity control layer on top of the foam.
調湿層は硬く焼固しでおり、釘でつついても壊れること
がなく、基層と化粧層とでしっかりと保持されていた。The humidity control layer was hard and hardened, did not break even when poked with a nail, and was firmly held by the base layer and decorative layer.
化粧層は白色の発泡粒よりなっており、各発泡粒はわず
かに発泡して粒の接点で溶着しているが、粒界を残して
連通気孔を保っていた。The decorative layer was made of white foamed grains, and each foamed grain was slightly foamed and welded at the contact points of the grains, but the grain boundaries remained and continuous pores were maintained.
化粧層の上方より水を落とすと瞬時には吸水しないが数
秒で吸水した。化粧層表面は小さな凹凸のある平面であ
り、凹んだ部分に連通気孔の端部があり、光沢のある化
粧セラミック板をうろことかできた。When water is dropped from above the makeup layer, it does not absorb water instantly, but it absorbs water within a few seconds. The surface of the decorative layer was a flat surface with small irregularities, and the concave portions had the ends of communicating holes, allowing the glossy decorative ceramic plate to be scaled.
実施例2
化粧層用造粒物の調製
白色煉瓦をクラッシャーで粗砕し、さらにロールクラッ
シャーで細粉砕して粒径0.5〜11Ilの粉砕粒をえ
た。えられた粉砕粒100重量部に対してC−3フリツ
ト(商品名。笠井釉薬銖製フリット)30重二部を、バ
インダー(イソパン3%溶液)を噴霧しながらパン型造
粒機を用いてコーティングした。Example 2 Preparation of Granulated Material for Decorative Layer A white brick was coarsely crushed using a crusher and further finely crushed using a roll crusher to obtain crushed granules having a particle size of 0.5 to 11 Il. To 100 parts by weight of the obtained crushed grains, 30 parts of C-3 frit (trade name: Frit manufactured by Kasai Glaze Co., Ltd.) was added using a pan-type granulator while spraying a binder (3% isopane solution). Coated.
こうしてコーティングされた造粒物を化粧層用造粒物と
して用いた以外は実施例1と同様にしてセラミック板を
製造した。A ceramic plate was produced in the same manner as in Example 1 except that the thus coated granules were used as the granules for the decorative layer.
えられたセラミック板の化粧層は光沢のある「じゅらく
壁」のような表面であった。白煉瓦の粉砕粒はガラス質
の皮で包まれて弱い光沢を有していた。各校はガラスの
表皮で融着しているが、実施例1における化粧層よりも
粒界が多く、水を上方より落下させると一瞬にして水は
吸水された。なお、実施例では透明であるが、コーティ
ングするフリットに着色すれば任意の色調をうろことが
できる。The decorative layer of the resulting ceramic plate had a shiny ``Juraku wall''-like surface. The crushed grains of white brick were encased in a glassy skin and had a weak luster. Each layer was fused by the glass skin, but there were more grain boundaries than in the decorative layer in Example 1, and when water was dropped from above, it was instantly absorbed. In the example, the coating is transparent, but if the frit to be coated is colored, any color tone can be obtained.
つぎに、実施例1でえられたセラミック板を301il
×301IIIlのサイズに切断し、木口および裏面を
シリコン樹脂にてシールを行いテストピースを作製した
。このテストピース1つずつを恒温恒湿層A(25℃、
40%R11)および恒温恒湿層B(25℃、80%R
11)の中に入れ、重量が一定になったのちに、恒温恒
湿層ASBのテストピースを入れ替えて、テストピース
の時間経過に伴う吸放湿量を測定した。結果を第3図に
示す。なお、比較のため杉(厚さ7.4mm)および無
機クロス十石膏ボード(厚さ9 am)についても同様
の試験を行った。Next, the ceramic plate obtained in Example 1 was heated to 301 il.
A test piece was prepared by cutting into a size of ×301III and sealing the end and back side with silicone resin. Each test piece was placed in constant temperature and humidity layer A (25℃,
40%R11) and constant temperature and humidity layer B (25℃, 80%R
11), and after the weight became constant, the test piece of the constant temperature and humidity layer ASB was replaced, and the amount of moisture absorption and desorption of the test piece over time was measured. The results are shown in Figure 3. For comparison, similar tests were conducted on cedar (thickness: 7.4 mm) and inorganic cloth gypsum board (thickness: 9 am).
吸放湿セラミック板は杉、および無機クロス十石膏ボー
ドに比べて、調湿速度および調湿容量がいずれも非常に
大きく、従来品よりも優れた調湿能力を示した。The moisture absorbing and desorbing ceramic board had a much greater humidity control speed and capacity than cedar and inorganic cloth gypsum boards, and showed better humidity control ability than conventional products.
[発明の効果]
以上説明したとおり、本発明のセラミック板によれば、
粒状の調湿原料を用いておらず、繊維ネットに泥漿状調
湿原料をコーティングしたシートを調湿層として用いて
いるので、セラミック板を切断したばあいに切断面より
調湿原料がこぼれ落ちることはなく、また調湿層部分の
強度も改善されるという効果かある。[Effects of the Invention] As explained above, according to the ceramic plate of the present invention,
Since we do not use granular humidity control raw materials and instead use a sheet of fiber net coated with slurry humidity control raw materials as the humidity control layer, when the ceramic board is cut, the humidity control raw materials will spill out from the cut surface. This has the effect of improving the strength of the humidity control layer.
第1図は本発明のセラミック板の一実施例の概略説明図
、第2a図は泥漿付着前の繊維ネットの概略説明図、第
2b図は泥漿付着後の繊維ネットの概略説明図、第3図
は実施例1にかかわるセラミック板、杉板および石膏ボ
ードの吸放湿量を測定した結果をあられす図である。FIG. 1 is a schematic explanatory diagram of an embodiment of the ceramic plate of the present invention, FIG. 2a is a schematic explanatory diagram of a fiber net before slurry is attached, FIG. 2b is a schematic explanatory diagram of a fiber net after slurry is attached, and FIG. The figure is a graph showing the results of measuring the amount of moisture absorption and release of the ceramic board, cedar board, and gypsum board according to Example 1.
(図面の主要符号) (1)二基 層 (2)、セラミックシート (3):化粧層(Main symbols on drawings) (1) Two layers (2) Ceramic sheet (3): Makeup layer
Claims (1)
基層と、該基層上に形成された、調湿原料を含む網目状
セラミックシートと、該セラミックシートの上に形成さ
れ、発泡性無機質造粒物を加熱発泡せしめた連通気孔性
の化粧層とからなり、前記基層、セラミックシートおよ
び化粧層が焼成により溶化一体化されてなることを特徴
とする調湿機能を有するセラミック板。 2前記調湿原料が活性アルミナを主成分とし、ゼオライ
トおよびセピオライトのうち少なくとも1種を含んでな
る請求項1記載のセラミック板。 3前記セラミックシートが有機質繊維からなるネットに
泥漿状態の調湿原料を付着せしめたものである請求項1
記載のセラミック板。 4調湿原料が付着したセラミックシートの網目の孔径が
、前記基層または化粧層を構成する発泡性無機質造粒物
の粒径よりも大きい請求項3記載のセラミック板。[Scope of Claims] 1. A closed-pore base layer formed by heating and foaming an expandable inorganic granule, a reticulated ceramic sheet containing a humidity control raw material formed on the base layer, and a reticulated ceramic sheet containing a humidity control raw material formed on the base layer; and a decorative layer with open pores formed by heating and foaming foamable inorganic granules, the base layer, the ceramic sheet, and the decorative layer being melted and integrated by firing. Ceramic plate with. 2. The ceramic plate according to claim 1, wherein the humidity control raw material contains activated alumina as a main component and at least one of zeolite and sepiolite. 3. Claim 1, wherein the ceramic sheet is a net made of organic fibers to which a humidity control raw material in a slurry state is adhered.
Ceramic plate as described. 4. The ceramic plate according to claim 3, wherein the pore size of the mesh of the ceramic sheet to which the humidity control raw material is attached is larger than the particle size of the expandable inorganic granules constituting the base layer or the decorative layer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2067460A JPH03266639A (en) | 1990-03-16 | 1990-03-16 | Ceramic sheet with moisture adjusting functionality |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2067460A JPH03266639A (en) | 1990-03-16 | 1990-03-16 | Ceramic sheet with moisture adjusting functionality |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH03266639A true JPH03266639A (en) | 1991-11-27 |
Family
ID=13345583
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2067460A Pending JPH03266639A (en) | 1990-03-16 | 1990-03-16 | Ceramic sheet with moisture adjusting functionality |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH03266639A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20030030262A (en) * | 2001-10-09 | 2003-04-18 | 주식회사세원콘크리트 | The method to product concrete interlocking block maked use of dolostone and the interlocking block |
-
1990
- 1990-03-16 JP JP2067460A patent/JPH03266639A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20030030262A (en) * | 2001-10-09 | 2003-04-18 | 주식회사세원콘크리트 | The method to product concrete interlocking block maked use of dolostone and the interlocking block |
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