JPH11199311A - Production of clay ceramic and caly ceramic - Google Patents
Production of clay ceramic and caly ceramicInfo
- Publication number
- JPH11199311A JPH11199311A JP10008538A JP853898A JPH11199311A JP H11199311 A JPH11199311 A JP H11199311A JP 10008538 A JP10008538 A JP 10008538A JP 853898 A JP853898 A JP 853898A JP H11199311 A JPH11199311 A JP H11199311A
- Authority
- JP
- Japan
- Prior art keywords
- clay
- ceramic
- water absorption
- glass
- firing
- 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 30
- 239000004927 clay Substances 0.000 title claims abstract description 20
- 238000004519 manufacturing process Methods 0.000 title claims description 15
- 101150040772 CALY gene Proteins 0.000 title 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 32
- 239000011521 glass Substances 0.000 claims abstract description 27
- 239000010433 feldspar Substances 0.000 claims abstract description 19
- 239000000454 talc Substances 0.000 claims abstract description 17
- 229910052623 talc Inorganic materials 0.000 claims abstract description 17
- 239000004576 sand Substances 0.000 claims abstract description 10
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 10
- 238000010304 firing Methods 0.000 claims description 39
- 238000000034 method Methods 0.000 claims description 10
- 239000002994 raw material Substances 0.000 claims description 8
- 239000000428 dust Substances 0.000 claims description 7
- 239000010922 glass waste Substances 0.000 claims description 4
- 238000001354 calcination Methods 0.000 claims description 3
- 229910052573 porcelain Inorganic materials 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 31
- 238000010521 absorption reaction Methods 0.000 abstract description 30
- 239000011148 porous material Substances 0.000 abstract description 12
- 229920006395 saturated elastomer Polymers 0.000 abstract description 12
- 238000000465 moulding Methods 0.000 abstract description 10
- 230000004907 flux Effects 0.000 abstract description 7
- 238000002156 mixing Methods 0.000 abstract description 7
- 239000005357 flat glass Substances 0.000 abstract description 4
- 239000006063 cullet Substances 0.000 abstract description 3
- 230000008602 contraction Effects 0.000 abstract 3
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 abstract 2
- 230000008014 freezing Effects 0.000 abstract 1
- 238000007710 freezing Methods 0.000 abstract 1
- 229910000029 sodium carbonate Inorganic materials 0.000 abstract 1
- 235000017550 sodium carbonate Nutrition 0.000 abstract 1
- 230000000052 comparative effect Effects 0.000 description 12
- 239000000440 bentonite Substances 0.000 description 5
- 229910000278 bentonite Inorganic materials 0.000 description 5
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 5
- 239000000758 substrate Substances 0.000 description 5
- 238000009835 boiling Methods 0.000 description 4
- 239000000155 melt Substances 0.000 description 4
- 238000011049 filling Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- KZHJGOXRZJKJNY-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Si]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O.O=[Al]O[Al]=O KZHJGOXRZJKJNY-UHFFFAOYSA-N 0.000 description 2
- 229910052634 enstatite Inorganic materials 0.000 description 2
- BBCCCLINBSELLX-UHFFFAOYSA-N magnesium;dihydroxy(oxo)silane Chemical compound [Mg+2].O[Si](O)=O BBCCCLINBSELLX-UHFFFAOYSA-N 0.000 description 2
- 229910052863 mullite Inorganic materials 0.000 description 2
- 238000007493 shaping process Methods 0.000 description 2
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 239000006004 Quartz sand Substances 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 238000005056 compaction Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000156 glass melt Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000006060 molten glass Substances 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 229910052611 pyroxene Inorganic materials 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 239000005361 soda-lime glass Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P40/00—Technologies relating to the processing of minerals
- Y02P40/60—Production of ceramic materials or ceramic elements, e.g. substitution of clay or shale by alternative raw materials, e.g. ashes
Landscapes
- Compositions Of Oxide Ceramics (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明はタイル、食器等の陶
磁器質セラミックスとその製造方法に係り、特に焼成収
縮が小さく、閉気孔率が高く吸水率が小さい陶磁器質セ
ラミックスとその製造方法に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to ceramic ceramics such as tiles and tableware, and a method for producing the same, and more particularly to a ceramic ceramic having a small firing shrinkage, a high closed porosity and a small water absorption, and a method for producing the same.
【0002】[0002]
【従来の技術】タルクを主原料としたステアタイト系陶
磁器は、吸水率3%以下となるまで焼き締めても、焼成
収縮が小さいことが知られている。このことは、特公昭
60−48268号公報第1欄第19行〜第2欄第1行
に記載されるように、成形時の粒子間隙が焼成後も閉気
孔として残っていることが原因と考えられている。な
お、閉気孔率とは、外形容積中の閉気孔容積の比率であ
り、2. Description of the Related Art It has been known that steatite ceramics made of talc as a main raw material have a small firing shrinkage even when baked to a water absorption of 3% or less. This is because, as described in JP-B-60-48268, column 1, line 19 to column 2, line 1, the particle gap during molding remains as closed pores even after firing. It is considered. Incidentally, the closed porosity is a ratio of the closed pore volume in the outer volume,
【0003】[0003]
【数1】 (Equation 1)
【0004】で算出される。ここで、W1:試料の乾燥
重量、W2:減圧吸水後の試料の水中重量、W3:減圧
吸水後の試料の重量、D:試料の真比重である。なお、
減圧吸水は、ISO10545−3の真空法に準拠して
行う。[0004] Here, W1: the dry weight of the sample, W2: the weight of the sample in water after absorbing the reduced pressure, W3: the weight of the sample after absorbing the reduced pressure, and D: the true specific gravity of the sample. In addition,
The reduced pressure water absorption is performed in accordance with the vacuum method of ISO10545-3.
【0005】また、ステアタイト系陶磁器の閉気孔の構
造は、特公平2−36543号公報第2図にあるよう
に、空洞孔が微細気孔によつてタイル表面とつながって
いることが知られている。As shown in FIG. 2 of Japanese Patent Publication No. 2-36543, it is known that the closed pore structure of steatite ceramics is such that hollow pores are connected to the tile surface by fine pores. I have.
【0006】ステアタイト系陶磁器の製造方法として
は、特公昭60−48268号公報、特公平2−365
43号公報等があるが、いずれもタルクを主原料とし、
成形助材として粘土、ベントナイトを、フラックスとし
て長石を使用している。このようにステアタイト系陶磁
器では、フラックスとして、長石を用いるのが一般的で
ある。この場合、焼成温度の1100〜1250℃は長
石が溶融を開始する温度領域であるため、まだ、フラッ
クス分の溶融粘性が高く、図1−Aのように、フラック
スによって埋められていない微細気孔が多く存在する。
このような素地の吸水を下げようとする場合、フラック
ス量を増加するか、焼成温度を上昇させることが一般的
であるが、この場合、収縮率が大きくなる難点がある。
この他にも、長石の溶融開始温度付近で焼成するため、
炉内の温度ばらつきや、原料の粉砕粒度、成形圧力のば
らつきに起因する成形体の充填等の微妙な違いで収縮
率、吸水率が変化しやすく、このため寸法や吸水率のば
らつきが大きくなるという問題もある。A method for producing steatite ceramics is disclosed in JP-B-60-48268, JP-B-2-365.
No. 43, etc., but all use talc as a main raw material,
Clay and bentonite are used as molding aids, and feldspar is used as flux. As described above, in steatite ceramics, feldspar is generally used as a flux. In this case, since the calcination temperature of 1100 to 1250 ° C. is a temperature range where feldspar starts melting, the melt viscosity of the flux is still high, and as shown in FIG. There are many.
In order to reduce the water absorption of such a substrate, it is common to increase the amount of flux or raise the firing temperature. However, in this case, there is a problem that the shrinkage rate increases.
In addition, since it is fired near the melting start temperature of feldspar,
Shrinkage and water absorption are likely to change due to subtle differences in furnace temperature, raw material pulverization particle size, and compaction of moldings due to variations in molding pressure, etc., and as a result, variations in dimensions and water absorption increase. There is also a problem.
【0007】ステアタイト系陶磁器にガラスを使用する
製造方法として、特公昭61−27347号公報には、
タルク35〜50重量部、ろう石17.5〜35重量
部、長石またはセリサイト17.5〜37.5重量部、
ベントナイト10重量部を混合、成形及び焼成する方法
が記載されている。なお、同号公報第4欄第18〜23
行には、さらに板ガラス、びんガラス等のカレットを添
加してもよいと記載されているが、このガラスカレット
の具体的な添加量については記載がない。Japanese Patent Publication No. 61-27347 discloses a production method using glass for steatite ceramics.
35 to 50 parts by weight of talc, 17.5 to 35 parts by weight of pyroxene, 17.5 to 37.5 parts by weight of feldspar or sericite,
A method of mixing, molding and firing 10 parts by weight of bentonite is described. The same publication, column 4, 18 to 23
The line states that cullet such as plate glass and bottle glass may be further added, but there is no description about the specific amount of glass cullet added.
【0008】特開昭55−113662号公報には、ガ
ラス屑約50wt%、タルク約40wt%、ベントナイ
ト約10wt%を混合、成形、焼成する陶磁器の製造方
法が記載されている。これは600〜1000℃で低温
焼成し寸法精度向上を図るためのものであるが、吸水率
が3%以上の場合ガラスの溶融量が少なく、素地の強度
を出しているエンスタタイトやムライトもこの温度では
ほとんど生成しないため十分な強度が得られない。ま
た、吸水率3%以下に焼き締めた場合、ガラスが多いた
め溶融粘性が低くなり、焼成時に素地が変形するという
問題がある。さらに、タルクは900〜1000℃で脱
水するため、この温度で焼成した場合、ガラス添加量が
50%と多いが、最高温度付近でタイル表面が溶融した
ガラスにおおわれてしまい、脱水した水蒸気がタイル中
から出られなくなり、タイル自体がレンズ状に膨らんで
しまう。また、1000℃以下で焼成する場合、一般に
その温度域で使用可能な釉薬の耐薬品性が悪くなるとい
う難点もある。Japanese Patent Application Laid-Open No. 55-113662 describes a method for producing ceramics by mixing, shaping and firing about 50 wt% of glass dust, about 40 wt% of talc, and about 10 wt% of bentonite. This is intended to improve the dimensional accuracy by firing at a low temperature of 600 to 1000 ° C. When the water absorption is 3% or more, the amount of glass melting is small, and enstatite and mullite, which provide the strength of the substrate, are also used. Sufficient strength cannot be obtained because it hardly forms at temperature. In addition, when baking is performed at a water absorption of 3% or less, there is a problem that the melt viscosity is low due to the large amount of glass, and the substrate is deformed during firing. Furthermore, since talc is dehydrated at 900 to 1000 ° C., when fired at this temperature, the amount of glass added is as large as 50%, but the tile surface is covered with molten glass near the maximum temperature, and the dehydrated steam is removed from the tile. You cannot get out of the room and the tile itself swells like a lens. In addition, when firing at 1000 ° C. or lower, there is also a disadvantage that the chemical resistance of a glaze usable in that temperature range generally deteriorates.
【0009】[0009]
【発明が解決しようとする課題】本発明は、耐凍害性を
有し、低収縮率、低吸水率であり、その結果として閉気
孔率が高く、しかも焼成温度や成形体の充填等の製造条
件のばらつきの影響の小さい陶磁器質セラミックスの製
造方法を提供することを目的とする。DISCLOSURE OF THE INVENTION The present invention relates to a method for manufacturing such as having a frost damage resistance, a low shrinkage rate, a low water absorption rate, a high closed porosity, a firing temperature, and filling of a molded article. An object of the present invention is to provide a method for producing a ceramic ceramic which is less affected by variations in conditions.
【0010】[0010]
【課題を解決するための手段】本発明の陶磁器質セラミ
ックスの製造方法は、 タルク 40〜65wt% 粘土 5〜30wt% ガラス屑 5〜45wt% 長石 0〜30wt% 珪砂及び/又はシャモット 0〜25wt% よりなる原料を混合し、成形及び焼成することを特徴と
するものである。Means for Solving the Problems The method for producing a ceramic ceramic according to the present invention is as follows. Characterized by mixing, shaping and firing.
【0011】本発明はタルク−粘土系主原料に対しガラ
スを適切量配合することにより、上記目的を達成するこ
とを見いだして完成されたものである。The present invention has been accomplished by finding that the above object can be achieved by blending an appropriate amount of glass with the talc-clay main raw material.
【0012】[0012]
【発明の実施の形態】まず本発明の原料の配合組成につ
いて説明する。DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS First, the composition of the raw materials of the present invention will be described.
【0013】本発明では、上記の通り、タルク40〜6
5wt%、粘土5〜30wt%、ガラス屑5〜45wt
%、長石0〜30wt%、珪砂及び/またはシャモット
0〜25wt%という配合を採用する。In the present invention, as described above, talc 40 to 6
5wt%, clay 5-30wt%, glass swarf 5-45wt
%, Feldspar 0-30 wt%, silica sand and / or chamotte 0-25 wt%.
【0014】このタルクはステアタイト系素地を形成す
る主原料である。このタルクの割合が40wt%より少
ないと、成形時の充填密度が低くなり、その結果、焼成
収縮が大きくなる。また、タルクが65wt%以上にな
ると、素地が過度に高耐火度のものとなり焼成温度が過
度に高くなる。この場合、焼成温度を1100〜125
0℃とした場合には、焼成が不十分となり、陶磁器の吸
水率が上昇してしまう。タルクの特に好ましい範囲は4
5〜55wt%である。This talc is a main raw material for forming a steatite base. If the proportion of talc is less than 40% by weight, the packing density at the time of molding becomes low, and as a result, firing shrinkage becomes large. On the other hand, if the talc is 65 wt% or more, the base becomes excessively high in fire resistance, and the firing temperature becomes excessively high. In this case, the firing temperature is set to 1100 to 125
When the temperature is set to 0 ° C., the sintering becomes insufficient, and the water absorption of the ceramics increases. A particularly preferred range of talc is 4
5 to 55 wt%.
【0015】粘土は成形助剤として機能するものであ
り、木節粘土、蛙目粘土、ベントナイト等を用いる。粘
土の割合が5wt%未満では成形体の強度が低い。一
方、粘土が30wt%よりも多くなると、溶融粘性が低
くなり、焼成時に素地の変形が大きくなる。粘土の配合
量は7〜25wt%、特に10〜20wt%が好まし
い。Clay functions as a molding aid, and includes Kibushi clay, Frogme clay, bentonite and the like. If the proportion of the clay is less than 5 wt%, the strength of the molded body is low. On the other hand, if the amount of the clay is more than 30% by weight, the melt viscosity becomes low, and the deformation of the base during firing becomes large. The compounding amount of the clay is preferably 7 to 25 wt%, particularly preferably 10 to 20 wt%.
【0016】ガラス屑は焼成温度を低下させるととも
に、収縮率を大きくしないで、焼成体の吸水率を低下さ
せる働きを有するものであるが、45wt%よりも多い
と1100〜1250℃の範囲では、焼成時に素地が溶
融して変形が大きくなる。一方、ガラス屑の添加量が5
wt%よりも少ないとガラス屑添加の効果が不十分とな
る。ガラス屑の特に好ましい配合量は7〜25wt%、
特に10〜20wt%である。Glass dust has the function of lowering the firing temperature and reducing the water absorption rate of the fired body without increasing the shrinkage, but if it is more than 45 wt%, in the range of 1100 ° C. to 1250 ° C. During firing, the substrate melts and deformation increases. On the other hand, when the amount of
If the amount is less than wt%, the effect of adding glass dust becomes insufficient. A particularly preferred blending amount of the glass dust is 7 to 25 wt%,
In particular, it is 10 to 20 wt%.
【0017】このガラス屑としては、ガラスが溶融し液
状を示す作業点が1050℃以下であるものが望まし
い。特に板ガラス屑、びんガラス屑等のソーダ石灰ガラ
スが望ましい。As the glass waste, it is desirable that the working point at which the glass melts and becomes liquid is 1050 ° C. or less. In particular, soda-lime glass such as sheet glass waste and bottle glass waste is desirable.
【0018】長石はフラックス成分となるものである。
この長石は任意添加成分であり、添加しなくてもよい。
長石を30wt%以下とし、とくに15wt%以下とす
るのが好ましい。Feldspar is a flux component.
This feldspar is an optional additive component and need not be added.
Feldspar is preferably at most 30 wt%, particularly preferably at most 15 wt%.
【0019】珪砂、シャモットは増量剤として用いられ
るものであり、任意添加成分である。珪砂、シャモット
の割合が25wt%よりも大きくなると吸水率が高くな
るので、珪砂、シャモットの量は合量で25wt%以下
とする。Silica sand and chamotte are used as extenders and are optional components. If the ratio of silica sand and chamotte is greater than 25 wt%, the water absorption rate increases, so the total amount of silica sand and chamotte is 25 wt% or less.
【0020】珪砂、シャモットについては、同じ役割を
するものとして、石英ガラス等のSiO2分の多いガラ
スを用いることも可能である。With respect to silica sand and chamotte, it is also possible to use glass having a high content of SiO 2 such as quartz glass as having the same role.
【0021】本発明では、これらの原料を、混合した後
成形し、焼成する。混合、焼成の方法は特に制限はな
い。焼成温度は1050〜1250℃、特に1160〜
1230℃が好ましい。In the present invention, these raw materials are mixed, molded, and fired. The method of mixing and firing is not particularly limited. The firing temperature is 1050 to 1250 ° C, particularly 1160 to 1250C.
1230 ° C. is preferred.
【0022】本発明方法においては、ガラス屑の割合を
5〜45wt%とし、焼成温度を1050〜1250℃
とすることにより、好ましくはガラス屑の割合を5〜3
5wt%として焼成温度を1160〜1230℃とする
ことにより、焼成収縮が飽和吸水率5%のとき2.4%
以下、閉気孔率12%以上、飽和吸水率1%のとき3.
5%以下、閉気孔率19.0%以上のきわめて低い収縮
率の陶磁器を製造することが可能となる。なお、飽和吸
水率はISO 10545−3の煮沸法に準拠する。In the method of the present invention, the proportion of glass swarf is 5 to 45 wt%, and the firing temperature is 1050 to 1250 ° C.
, Preferably, the ratio of the glass waste is 5 to 3
By setting the firing temperature to 1160 to 1230 ° C. at 5 wt%, the firing shrinkage is 2.4% when the saturated water absorption is 5%.
Hereinafter, when the closed porosity is 12% or more and the saturated water absorption is 1%.
It is possible to manufacture a ceramic having an extremely low shrinkage of 5% or less and a closed porosity of 19.0% or more. The saturated water absorption is based on the boiling method of ISO 10545-3.
【0023】この理由としては以下のようである。陶磁
器の寸法精度を上げる一つの方法として、前述したよう
に、焼成後の素地中の閉気孔を増やすことにより、かさ
密度を下げる方法がある。タルクを用いた素地には、特
公平2−36543号公報第2図にあるように、素地中
に空洞孔と微細気孔を持つことが知られている。今回使
用しているガラスは、焼成温度の1100℃以上での溶
融粘性が低いため、長石と比べ微細気孔を埋めやすい。
このため、図1に示すように、長石を使用した場合に、
微細気孔を介して外部とつながっている内部気孔が、ガ
ラスを用いた場合閉気孔となる。このため、閉気孔率が
増加し、かさ密度が下がるため、低収縮となり、寸法精
度が上がっているのである。また、1050℃以上の温
度で焼成しているためエンスタタイトが生成され、ま
た、1160℃以上で焼成する場合には、ムライトも生
成されるため、十分な強度が得られる。The reason is as follows. One method for increasing the dimensional accuracy of ceramics is to reduce the bulk density by increasing the number of closed pores in the fired body, as described above. As shown in FIG. 2 of Japanese Patent Publication No. 2-36543, it is known that a base using talc has hollow holes and fine pores in the base. The glass used this time has a low melt viscosity at a firing temperature of 1100 ° C. or higher, so that it is easier to fill fine pores than feldspar.
Therefore, as shown in FIG. 1, when feldspar is used,
The internal pores connected to the outside through the fine pores become closed pores when glass is used. As a result, the closed porosity increases and the bulk density decreases, resulting in low shrinkage and increased dimensional accuracy. In addition, enstatite is generated because it is fired at a temperature of 1050 ° C. or more, and mullite is generated when it is fired at a temperature of 1160 ° C. or more, so that sufficient strength is obtained.
【0024】[0024]
【実施例】実施例1、比較例1〜4 タルク、ベントナイト、粘土、珪砂、ガラス屑、長石、
蝋石を表1の割合で配合した。ここで、比較例1,2及
び比較例3,4はそれぞれ、特公昭60−48468号
公報、特公昭61−27347号公報に記載されたもの
である。これをボールミルで4hr粉砕、混合後、乾
燥、含水、造粒し、プレス成形(面圧30MPa)し、
100×100×5mmの成形体とした。これを迅速焼
成炉で1100℃、30分の条件で素焼きを行い、施釉
後、1200℃、50分で迅速焼成した。この焼成に伴
う収縮量を測定して収縮率を計算するとともに、飽和吸
水率、閉気孔率を測定した。結果を表1に示す。EXAMPLES Example 1, Comparative Examples 1-4 Talc, bentonite, clay, quartz sand, glass swarf, feldspar,
Rouseki was blended in the proportions shown in Table 1. Here, Comparative Examples 1 and 2 and Comparative Examples 3 and 4 are described in Japanese Patent Publication No. 60-48468 and Japanese Patent Publication No. 61-27347, respectively. This was pulverized by a ball mill for 4 hours, mixed, dried, hydrated, granulated, and press-molded (surface pressure: 30 MPa).
A molded body of 100 × 100 × 5 mm was obtained. This was unbaked in a rapid firing furnace at 1100 ° C. for 30 minutes, and after glazing, quickly fired at 1200 ° C. for 50 minutes. The shrinkage due to the firing was measured to calculate the shrinkage, and the saturated water absorption and closed porosity were measured. Table 1 shows the results.
【0025】実施例2、比較例5 タルク、木節粘土、板ガラス屑、長石及び珪砂を表2の
割合で配合し、実施例1、比較例1〜4と同様の方法で
粉砕から素焼きを行い、施釉後、1170,1190,
または1210℃、50分で迅速焼成した。この焼成に
伴う収縮率、飽和吸水率を測定した。結果を表2に示
す。また、相関関係を図2にまとめた。Example 2, Comparative Example 5 Talc, Kibushi clay, sheet glass scrap, feldspar and silica sand were blended in the proportions shown in Table 2, and ground and unbaked in the same manner as in Example 1, Comparative Examples 1-4. After glazing, 1170, 1190,
Alternatively, it was quickly fired at 1210 ° C. for 50 minutes. The shrinkage and the saturated water absorption due to this firing were measured. Table 2 shows the results. FIG. 2 shows the correlation.
【0026】実施例3、比較例6 タルク、木節粘土、板ガラス屑、長石、珪砂を表3の割
合で配合し、ボールミルで平均粒径(D50)が12ミ
クロンになるまで粉砕し、乾燥、含水、造粒後、プレス
成形(面圧28,30,32MPa)し、100×10
0×5mmの成形体とした。これを迅速焼成炉で110
0℃、30分の条件で仮焼(素焼き)を行い、施釉後、
1200℃、50分で迅速焼成した。この焼成に伴う収
縮率と煮沸吸水率、閉気孔率を表3に示す。Example 3, Comparative Example 6 Talc, Kibushi clay, glass swarf, feldspar, and silica sand were blended in the proportions shown in Table 3 and pulverized in a ball mill until the average particle diameter (D50) became 12 microns, and dried. After being hydrated and granulated, press-molding (contact pressure 28, 30, 32 MPa), 100 × 10
A molded body of 0 × 5 mm was obtained. This is put in a rapid firing furnace for 110
Perform calcination (unglazed) at 0 ° C for 30 minutes, and after glazing,
Rapid firing was performed at 1200 ° C. for 50 minutes. Table 3 shows the shrinkage rate, boiling water absorption rate, and closed porosity associated with the firing.
【0027】実施例4〜6 タルク、木節粘土、板ガラス屑、シャモットを表4の割
合で配合し、ボールミルで4H粉砕し、乾燥、含水、造
粒後、プレス成形(面圧30MPa)し、100×10
0×8.5mmの成形体とした。これを施釉後、迅速焼
成炉でそれぞれの試料の飽和吸水率がほぼ、5%,1%
となる条件で焼成した。この焼成に伴う収縮率と煮沸吸
水率、閉気孔率を表4に示す。Examples 4 to 6 Talc, Kibushi clay, glass swarf, and chamotte were blended in the proportions shown in Table 4, pulverized by a ball mill for 4H, dried, hydrated, granulated, and press-molded (surface pressure: 30 MPa). 100 × 10
A molded body of 0 × 8.5 mm was obtained. After glazing, the saturated water absorption of each sample is approximately 5% and 1% in a rapid firing furnace.
The firing was performed under the following conditions. Table 4 shows the shrinkage, boiling water absorption, and closed porosity associated with the firing.
【0028】[0028]
【表1】 [Table 1]
【0029】実施例1は比較例1〜4と比較して閉気孔
率が高い。比較例1,2は低収縮だが飽和吸水率が高
く、その結果として閉気孔率が低い。比較例3,4と実
施例1はほぼ同じ飽和吸水率であるが、実施例1が最も
低収縮である。このことが閉気孔率の差に反映されてい
る。Example 1 has a higher closed porosity than Comparative Examples 1 to 4. Comparative Examples 1 and 2 have low shrinkage but high saturated water absorption, and consequently low closed porosity. Comparative Examples 3 and 4 and Example 1 have almost the same saturated water absorption, but Example 1 has the lowest shrinkage. This is reflected in the difference in closed porosity.
【0030】[0030]
【表2】 [Table 2]
【0031】実施例2と比較例5との対比から明らかな
とおり、ガラス屑を添加することにより収縮率及び飽和
吸水率がいずれも顕著に低下する。また、焼成温度が1
170〜1210℃の間で変えても変動幅が小さいこと
が認められる。また、どの温度水準でもガラス屑を用い
た方が閉気孔率が高い。As is clear from the comparison between Example 2 and Comparative Example 5, the addition of glass dust significantly reduces both the shrinkage and the saturated water absorption. When the firing temperature is 1
It is recognized that the fluctuation range is small even when the temperature is changed between 170 to 1210 ° C. In addition, the closed porosity is higher when glass dust is used at any temperature level.
【0032】[0032]
【表3】 [Table 3]
【0033】実施例3と比較例4の対比から明らかなよ
うに、ガラスを用いた場合、長石を用いた時よりも圧
力、すなわち、成形体の充填の変化に対して収縮率、煮
沸吸水率の変化が小さいことがわかる。As is evident from the comparison between Example 3 and Comparative Example 4, when glass is used, the shrinkage ratio and the boiling water absorption ratio with respect to the change in the pressure, that is, the change in filling of the compact, are higher than when feldspar is used. Is small.
【0034】[0034]
【表4】 [Table 4]
【0035】実施例4〜6にあるように、ガラス量を増
やすことによって耐火度が下がり、より低い温度で飽和
吸水率を下げることが可能である。このことから、ガラ
ス添加量によって焼成温度をかえることにより、目的の
吸水をもった試料が得られることが分かる。As in Examples 4 to 6, the fire resistance is reduced by increasing the amount of glass, and it is possible to lower the saturated water absorption at a lower temperature. From this, it can be seen that a sample having the desired water absorption can be obtained by changing the firing temperature depending on the amount of glass added.
【0036】[0036]
【発明の効果】以上の通り、本発明の陶磁器質セラミッ
クスの製造方法によると、低収縮率、低吸水率であり、
しかも焼成温度や素地の充填等の変化の影響が小さい陶
磁器を製造することができる。As described above, according to the method for producing a ceramic ceramic of the present invention, a low shrinkage rate and a low water absorption rate are obtained.
In addition, it is possible to manufacture a porcelain that is less affected by changes in the firing temperature and the filling of the substrate.
【図1】長石、ガラスをフラックスとして用いた際の焼
成後の素地の概念を示した図である。FIG. 1 is a view showing the concept of a green body after firing when feldspar and glass are used as a flux.
【図2】実施例2、比較例5の測定結果を示すグラフで
ある。FIG. 2 is a graph showing measurement results of Example 2 and Comparative Example 5.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 岡本 健児 愛知県常滑市鯉江本町5丁目1番地 株式 会社イナックス内 (72)発明者 秋田 勝彦 東京都板橋区双葉町12−4 ──────────────────────────────────────────────────続 き Continued on the front page (72) Inventor Kenji Okamoto 5-1-1 Koiehonmachi, Tokoname-shi, Aichi Inax Inc. (72) Inventor Katsuhiko Akita 12-4 Futabacho, Itabashi-ku, Tokyo
Claims (4)
する陶磁器質セラミックスの製造方法。1. A raw material comprising 40 to 65 wt% of talc, 5 to 30 wt% of clay, 5 to 45 wt% of glass dust, 0 to 30 wt% of feldspar and 0 to 25 wt% of silica sand and / or chamotte are mixed, molded and fired. Method of producing ceramic ceramics.
〜1250℃であることを特徴とする陶磁器質セラミッ
クスの製造方法。2. The method according to claim 1, wherein the firing temperature is 1050.
A method for producing a ceramic ceramic, wherein the temperature is 1250C.
1250℃で本焼成することを特徴とする陶磁器質セラ
ミックスの製造方法。3. The method according to claim 2, wherein after calcining, the amount is 1050 to 1050.
A method for producing porcelain ceramics, characterized by firing at 1250 ° C.
て、ガラス屑の割合が5〜35wt%であり、焼成温度
が1160〜1230℃であることを特徴とする陶磁器
質セラミックスの製造方法。4. The method for producing a ceramic ceramic according to claim 1, wherein the proportion of glass waste is 5 to 35 wt% and the firing temperature is 1160 to 1230 ° C.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10008538A JPH11199311A (en) | 1998-01-20 | 1998-01-20 | Production of clay ceramic and caly ceramic |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP10008538A JPH11199311A (en) | 1998-01-20 | 1998-01-20 | Production of clay ceramic and caly ceramic |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH11199311A true JPH11199311A (en) | 1999-07-27 |
Family
ID=11695940
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP10008538A Pending JPH11199311A (en) | 1998-01-20 | 1998-01-20 | Production of clay ceramic and caly ceramic |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH11199311A (en) |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007217929A (en) * | 2006-02-15 | 2007-08-30 | Ig Tech Res Inc | Wave absorber |
| RU2477715C1 (en) * | 2012-02-22 | 2013-03-20 | Юлия Алексеевна Щепочкина | Ceramic mixture for making buttons |
| KR101409186B1 (en) * | 2012-11-09 | 2014-06-20 | 한국세라믹기술원 | Manufacturing method of the lightweight ceramic ware using the composite for lightweight ceramic ware comprising talc |
| RU2521107C1 (en) * | 2013-06-14 | 2014-06-27 | Юлия Алексеевна Щепочкина | Mixture for brick manufacture |
| JP2014166946A (en) * | 2013-02-04 | 2014-09-11 | Takahama Industry Co Ltd | Glass powder and method of producing pottery using the same as part of raw material |
| JP2014227305A (en) * | 2013-05-17 | 2014-12-08 | パナホーム株式会社 | Lightweight tile and manufacturing method therefor |
| KR101713438B1 (en) * | 2015-09-15 | 2017-03-07 | 권혁이 | Producing method of eco-friendly lightweight tiles using waste coal tailings |
| JP2017154934A (en) * | 2016-03-02 | 2017-09-07 | 黒崎播磨株式会社 | Heat insulation tile and manufacturing method therefor |
| CN111606699A (en) * | 2020-06-04 | 2020-09-01 | 景德镇陶瓷大学 | A kind of lightweight porous daily-use fine porcelain and preparation method thereof |
| CN116553920A (en) * | 2023-05-12 | 2023-08-08 | 清远市简一陶瓷有限公司 | Low-temperature quick-firing ceramic tile blank and preparation process of low-temperature quick-firing marble ceramic tile using same |
| EP4084958A4 (en) * | 2019-12-31 | 2024-02-21 | Seramic Materials Limited | Industrial solid waste based construction and technical ceramics |
-
1998
- 1998-01-20 JP JP10008538A patent/JPH11199311A/en active Pending
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007217929A (en) * | 2006-02-15 | 2007-08-30 | Ig Tech Res Inc | Wave absorber |
| RU2477715C1 (en) * | 2012-02-22 | 2013-03-20 | Юлия Алексеевна Щепочкина | Ceramic mixture for making buttons |
| KR101409186B1 (en) * | 2012-11-09 | 2014-06-20 | 한국세라믹기술원 | Manufacturing method of the lightweight ceramic ware using the composite for lightweight ceramic ware comprising talc |
| JP2014166946A (en) * | 2013-02-04 | 2014-09-11 | Takahama Industry Co Ltd | Glass powder and method of producing pottery using the same as part of raw material |
| JP2014227305A (en) * | 2013-05-17 | 2014-12-08 | パナホーム株式会社 | Lightweight tile and manufacturing method therefor |
| RU2521107C1 (en) * | 2013-06-14 | 2014-06-27 | Юлия Алексеевна Щепочкина | Mixture for brick manufacture |
| KR101713438B1 (en) * | 2015-09-15 | 2017-03-07 | 권혁이 | Producing method of eco-friendly lightweight tiles using waste coal tailings |
| JP2017154934A (en) * | 2016-03-02 | 2017-09-07 | 黒崎播磨株式会社 | Heat insulation tile and manufacturing method therefor |
| EP4084958A4 (en) * | 2019-12-31 | 2024-02-21 | Seramic Materials Limited | Industrial solid waste based construction and technical ceramics |
| US11964914B2 (en) | 2019-12-31 | 2024-04-23 | Seramic Materials Limited | Industrial solid waste based construction and technical ceramics |
| CN111606699A (en) * | 2020-06-04 | 2020-09-01 | 景德镇陶瓷大学 | A kind of lightweight porous daily-use fine porcelain and preparation method thereof |
| CN111606699B (en) * | 2020-06-04 | 2023-01-24 | 景德镇陶瓷大学 | A kind of lightweight porous daily-use fine porcelain and its preparation method |
| CN116553920A (en) * | 2023-05-12 | 2023-08-08 | 清远市简一陶瓷有限公司 | Low-temperature quick-firing ceramic tile blank and preparation process of low-temperature quick-firing marble ceramic tile using same |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US9290409B2 (en) | Glaze composition, method for manufacturing the glaze composition and methods of glazing | |
| Zanelli et al. | Glass–ceramic frits for porcelain stoneware bodies: Effects on sintering, phase composition and technological properties | |
| JPH04124059A (en) | ceramic tiles | |
| US4300953A (en) | Dense cordierite containing manganese | |
| JPH11199311A (en) | Production of clay ceramic and caly ceramic | |
| JP4155284B2 (en) | Tile, its manufacturing method and tile raw material | |
| JP2000128671A (en) | Glazed ceramic and its production | |
| HK1212318A1 (en) | Large ceramic plate | |
| JP5659883B2 (en) | Humidity control building material and manufacturing method thereof | |
| KR101095027B1 (en) | Alumina binder amorphous refractory and preparation method thereof | |
| JP2003137639A (en) | Porcelain clay for ceramic, ceramic, and production method therefor | |
| JPH07237958A (en) | High-strength porcelain and production thereof | |
| JP2582730B2 (en) | Manufacturing method of ceramic molded products | |
| JP3111741B2 (en) | High strength porcelain and its manufacturing method | |
| JP3949408B2 (en) | Silica brick for hot repair and its manufacturing method | |
| JP2002068822A (en) | Sanitary ware | |
| JP2001206763A (en) | China and porcelain | |
| JP2001220260A (en) | Alumina-based porous sheet refractory and method for producing the same | |
| KR102918141B1 (en) | Composition for sanitary ceramics and sanitary ceramics using thereof | |
| KR101265944B1 (en) | Composite for ceramic ware including oxide pigment and manufacturing method of ceramic ware using the pigment | |
| KR20120103473A (en) | Moisture control construction material and method of manufacturing the same | |
| Wasanapiarnpong et al. | Application of Soda-Lime-Silica Cullet as a Fluxing Component in a Vitreous China Ware Casting Body | |
| JP3173657B2 (en) | Ceramic products and their manufacturing methods | |
| JP2002255630A (en) | Sanitary chinaware | |
| JP2002068821A (en) | Sanitary ware |