JP2000319082A - Sanitary ware - Google Patents

Sanitary ware

Info

Publication number
JP2000319082A
JP2000319082A JP11127883A JP12788399A JP2000319082A JP 2000319082 A JP2000319082 A JP 2000319082A JP 11127883 A JP11127883 A JP 11127883A JP 12788399 A JP12788399 A JP 12788399A JP 2000319082 A JP2000319082 A JP 2000319082A
Authority
JP
Japan
Prior art keywords
glaze layer
metal oxide
glaze
weight
component
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.)
Granted
Application number
JP11127883A
Other languages
Japanese (ja)
Other versions
JP3783466B2 (en
Inventor
Yutaka Tomioka
豊 冨岡
Satoshi Horiuchi
堀内  智
Shingo Kasahara
慎吾 笠原
Shigeyuki Yamada
茂幸 山田
Toru Ueno
徹 上野
Hiroyuki Takada
高田  宏行
Yukinari Matsumoto
幸成 松本
Toshimitsu Suda
稔光 須田
Katsuhiro Kawakami
克博 川上
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Toto Ltd
Original Assignee
Toto Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Toto Ltd filed Critical Toto Ltd
Priority to JP12788399A priority Critical patent/JP3783466B2/en
Publication of JP2000319082A publication Critical patent/JP2000319082A/en
Application granted granted Critical
Publication of JP3783466B2 publication Critical patent/JP3783466B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/009After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone characterised by the material treated
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/45Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
    • C04B41/50Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with inorganic materials
    • C04B41/5022Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with inorganic materials with vitreous materials

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Sanitary Device For Flush Toilet (AREA)
  • Glass Compositions (AREA)

Abstract

PROBLEM TO BE SOLVED: To maintain surface roughness at a specific value or below in spite of variations in production and to minimize the defects in production, such as appearance defects, by forming a first glaze layer having a specific compounded composition containing coloring pigment on the surface of an earthenware body and forming a second glaze layer having a specific compound composition free of the coloring pigment thereon. SOLUTION: The surface roughness of the resulted earthenware is suppressed to <0.07 μm. The components of the first glaze layer are, by weight % with respect to the glass components, 55 to 80 SiO2 component, 5 to 13 Al2O3 component, 10 to 25 bivalent metal oxide, 1.5 to 6.5 univalent metal oxide and 0.1 to 15 opacifier. The components of the second glaze layer are 52 to 76 SiO2 component, 6 to 14 Al2O3 component, 13 to 28 bivalent metal oxide and 1.5 to 6.5 univalent metal oxide. The first glaze layer 2 is applied on the sanitary ware body 1 and thereafter, the second glaze layer 3 is applied thereon.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は長期に渡って汚れを
容易に除去しうる機能を維持するため、焼成過程におい
て発生する外観上の欠点を軽減した大便器・小便器・手
洗い器・洗面器などの衛生陶器の製造方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a toilet bowl, a urinal bowl, a hand-washing bowl, and a basin, which have a function of easily removing dirt over a long period of time and have reduced appearance defects that occur during a firing process. And a method for manufacturing sanitary ware.

【0002】[0002]

【従来の技術】従来、大便器・小便器・手洗い器・洗面
器などの衛生陶器では、一般的に成形素地に釉薬をスプ
レー等により1層塗布し、成形素地が充分に焼結する温
度で釉薬が軟化して下地の陶器素地に固着されるように
焼成することにより得られていた。また、釉薬原料とし
ては、天然原料である珪石、長石等を主原料とし、その
他乳濁剤としてジルコン、ジルコニア、酸化錫等を添加
していた。
2. Description of the Related Art Conventionally, in sanitary ware such as toilets, urinals, hand-washers, washbasins, etc., one layer of glaze is generally applied to a molding base by spraying or the like at a temperature at which the molding base is sufficiently sintered. It has been obtained by firing such that the glaze softens and adheres to the underlying pottery substrate. As a glaze material, natural materials such as silica stone and feldspar were used as main materials, and zircon, zirconia, tin oxide and the like were added as emulsifiers.

【0003】[0003]

【発明が解決しようとする課題】しかし上記のような従
来の方法では、釉薬層中の石英やジルコンおよび顔料の
粒子のため、表面粗さ(Ra)が触針式表面粗さ測定装
置(JIS−B0651)により0.07μm以上であ
り、長期に渡って汚れを容易に除去しうる機能を維持す
ることが困難であった。
However, in the conventional method as described above, the surface roughness (Ra) is measured by a stylus type surface roughness measuring device (JIS) due to the particles of quartz, zircon and pigment in the glaze layer. -B0651), it was 0.07 μm or more, and it was difficult to maintain the function of easily removing dirt over a long period of time.

【0004】[0004]

【課題を解決するための手段】そこでこの問題を解決す
るために、本出願人は、成形素地上に第一の釉薬層と第
二の釉薬層を設け、第二の釉薬層には予め溶融された非
晶質釉薬を用いることおよび微粒化により焼成後の残留
石英量を極力低減させる方法(平成10年特許願第16
4177号)、また第二の釉薬層にはジルコンと顔料の
添加を行わない方法等(特願平10−371599)を
提案した。
Therefore, in order to solve this problem, the present applicant has provided a first glaze layer and a second glaze layer on a molding base, and the second glaze layer has been previously melted. Method for minimizing the amount of residual quartz after firing by using an amorphous glaze that has been obtained and by atomization (Japanese Patent Application No. 16/1998)
No. 4177), and a method of not adding zircon and pigment to the second glaze layer (Japanese Patent Application No. 10-371599).

【0005】本出願人は、上記発明をさらに検討した結
果、製造上のバラツキに拘らず、表面粗さが0.07mm
未満を維持しつつ斑点模様や亀甲模様等の外観不良が発
生しにくい条件が存在することを見出した。
As a result of further study of the above-mentioned invention, the present applicant has found that the surface roughness is 0.07 mm regardless of manufacturing variations.
It has been found that there is a condition in which poor appearance such as a spotted pattern or a turtle pattern is less likely to occur while maintaining a value of less than.

【0006】本発明の実施態様においては、衛生陶器素
地表面に、着色性の第一の釉薬層が形成されており、さ
らにその上に透明性の第二の釉薬層が形成されている衛
生陶器において、前記第一の釉薬層の成分がSiO2、
Al2O3、2価金属酸化物、1価金属酸化物及び乳濁
剤から成っており、前記SiO2のガラス成分に対する
重量%が55〜80%であり、前記Al2O3のガラス
成分に対する重量%が5〜13%であり、前記2価金属
酸化物のガラス成分に対する重量%が10〜25%であ
り、前記1価金属酸化物のガラス成分に対する重量%が
1.5〜6.5%であり、且つ乳濁剤のガラス成分に対す
る重量%が0.1〜15%であり、前記第二の釉薬層の
成分がSiO2、Al2O3、2価金属酸化物及び1価
金属酸化物から成っており、前記SiO2のガラス成分
に対する重量%が52〜76%であり、前記Al2O3
のガラス成分に対する重量%が6〜14%であり、前記
2価金属酸化物のガラス成分に対する重量%が13〜2
8%であり、前記1価金属酸化物のガラス成分に対する
重量%が1.5〜6.5%である衛生陶器を提供する。
かかる衛生陶器は、非常に光沢があり且つ表面粗さが
0.07μm未満、好ましくは0.05μm未満、より好
ましくは0.03μm未満を維持し得る。従って、長期
に渡って汚れを容易に除去しうる機能を維持する。
In an embodiment of the present invention, a sanitary ware in which a first colored glaze layer is formed on the surface of the sanitary ware body and a transparent second glaze layer is formed thereon. In the above, the component of the first glaze layer is SiO2,
Al2O3, a divalent metal oxide, a monovalent metal oxide, and an emulsifier, wherein the weight% of the SiO2 to the glass component is 55 to 80%, and the weight% of the Al2O3 to the glass component is 5 to 13%. %, The weight% of the divalent metal oxide with respect to the glass component is 10 to 25%, the weight% of the monovalent metal oxide with respect to the glass component is 1.5 to 6.5%, and The weight% of the turbidity agent with respect to the glass component is 0.1 to 15%, and the component of the second glaze layer is composed of SiO2, Al2O3, divalent metal oxide and monovalent metal oxide. The weight percentage of the glass component is 52 to 76%, and the Al 2 O 3
Is 6 to 14% by weight based on the glass component, and 13 to 2% by weight based on the glass component of the divalent metal oxide.
A sanitary ware, which is 8%, and the weight% of the monovalent metal oxide with respect to the glass component is 1.5 to 6.5%.
Such sanitary ware can be very shiny and maintain a surface roughness of less than 0.07 μm, preferably less than 0.05 μm, more preferably less than 0.03 μm. Therefore, the function of easily removing dirt is maintained for a long time.

【0007】前記第二の釉薬層の成分の内、SiO2の
ガラス成分に対する重量%が52%未満である場合、特
に大便器のトラップ部、小便器のトラップ部等に釉溜ま
りが発生し、所望の釉薬面が得られない。これは、前記
第二の釉薬層の最高温度での粘性が第一の釉薬層の最高
温度での粘性に比べて低すぎるためと考えられる。これ
はSiO2量減少のため、SiO2粒子が完全に周囲の
ガラスに溶解してしまうことで、完全にニュートン流体
としての挙動を示してしまう可能性が示唆される。
If the weight percentage of SiO2 relative to the glass component in the second glaze layer component is less than 52%, glaze accumulation occurs particularly in the trap portion of the toilet and the trap portion of the urinal. Glaze surface cannot be obtained. This is probably because the viscosity of the second glaze layer at the highest temperature is too low compared to the viscosity of the first glaze layer at the highest temperature. This suggests that the SiO2 particles may completely dissolve in the surrounding glass due to the decrease in the amount of SiO2, and thus may completely exhibit the behavior as a Newtonian fluid.

【0008】前記第二の釉薬層の成分の内、SiO2の
ガラス成分に対する重量%が76%以上である場合、特
に大便器のボール面、小便器のボール面等に亀甲模様が
発生し、所望の釉薬面が得られない。これは、前記第二
の釉薬層の最高温度での粘性が第一の釉薬層の最高温度
での粘性に比べて高すぎるためと考えられる。この理由
はSiO2量増加のため、SiO2粒子が完全にガラス
に溶解できずに、未溶解シリカとしてかなりの量残存し
てしまうため、ガラスと未溶解シリカとの間に摩擦が働
いている可能性が示唆される。
When the weight percentage of SiO2 in the glass component of the second glaze layer is 76% or more, a turtle pattern is formed on the ball surface of a toilet bowl, the ball surface of a urinal, and the like. Glaze surface cannot be obtained. This is probably because the viscosity of the second glaze layer at the maximum temperature is too high compared to the viscosity of the first glaze layer at the maximum temperature. The reason for this is that, due to an increase in the amount of SiO2, the SiO2 particles cannot be completely dissolved in the glass but remain in a considerable amount as undissolved silica, so that friction may be acting between the glass and the undissolved silica. Is suggested.

【0009】前記第二の釉薬層の成分の内、Al2O3
のガラス成分に対する重量%が6%未満である場合、マ
ット状模様が発生し、所望の釉薬面が得られない。これ
は、前記第二の釉薬層の最高温度での粘性が第一の釉薬
層の最高温度での粘性に比べて高すぎるためと考えられ
る。この理由はAl2O3量減少により相対的に増加し
たSiO2粒子が完全にガラスに溶解できずに、未溶解
シリカとしてかなりの量残存してしまうため、ガラスと
未溶解シリカとの間に摩擦が働いている可能性が示唆さ
れる。
[0009] Among the components of the second glaze layer, Al2O3
When the weight% of the glass component is less than 6%, a mat-like pattern is generated, and a desired glaze surface cannot be obtained. This is probably because the viscosity of the second glaze layer at the maximum temperature is too high compared to the viscosity of the first glaze layer at the maximum temperature. The reason for this is that the SiO2 particles relatively increased due to the decrease in the amount of Al2O3 cannot be completely dissolved in the glass but remain in a considerable amount as undissolved silica, so that friction acts between the glass and the undissolved silica. It is suggested that there is a possibility.

【0010】前記第二の釉薬層の成分の内、Al2O3
のガラス成分に対する重量%が14%以上である場合、
マット状模様が発生し、所望の釉薬面が得られない。こ
れは、前記第二の釉薬層の最高温度での粘性が第一の釉
薬層の最高温度での粘性に比べて高すぎるためと考えら
れる。この理由はAl2O3量増加により析出されたム
ライト結晶とガラスと間に摩擦が働いている可能性が示
唆される。
[0010] Among the components of the second glaze layer, Al2O3
When the weight% of the glass component is 14% or more,
A mat-like pattern is generated, and a desired glaze surface cannot be obtained. This is probably because the viscosity of the second glaze layer at the maximum temperature is too high compared to the viscosity of the first glaze layer at the maximum temperature. The reason for this suggests that friction may be acting between the mullite crystals precipitated by increasing the amount of Al2O3 and the glass.

【0011】前記第二の釉薬層の成分の内、前記2価金
属酸化物のガラス成分に対する重量%が13%未満であ
る場合、マット状模様が発生し、所望の釉薬面が得られ
ない。これは、前記第二の釉薬層の最高温度での粘性が
第一の釉薬層の最高温度での粘性に比べて高すぎるため
と考えられる。この理由は2価金属酸化物量減少により
相対的に増加したSiO2粒子が完全にガラスに溶解で
きずに、未溶解シリカとしてかなりの量残存してしまう
ため、ガラスと未溶解シリカとの間に摩擦が働いている
可能性が示唆される。
If the weight percentage of the divalent metal oxide relative to the glass component in the second glaze layer component is less than 13%, a mat-like pattern is generated and a desired glaze surface cannot be obtained. This is probably because the viscosity of the second glaze layer at the maximum temperature is too high compared to the viscosity of the first glaze layer at the maximum temperature. The reason is that the SiO2 particles relatively increased due to the decrease in the amount of the divalent metal oxide cannot be completely dissolved in the glass and remain in a considerable amount as undissolved silica. It is suggested that may be working.

【0012】前記第二の釉薬層の成分の内、前記2価金
属酸化物のガラス成分に対する重量%が28%以上であ
る場合、マット状模様が発生し、所望の釉薬面が得られ
ない。これは、前記第二の釉薬層の最高温度での粘性が
第一の釉薬層の最高温度での粘性に比べて高すぎるため
と考えられる。この理由は前記2価金属酸化物量増加に
より析出された結晶、特に前記2価金属酸化物としてZ
nOを使用した場合に析出するウィレマイトとガラスと
の間に摩擦が働いている可能性が示唆される。
If the weight percent of the divalent metal oxide in the glass component of the second glaze layer is 28% or more, a mat-like pattern is generated, and a desired glaze surface cannot be obtained. This is probably because the viscosity of the second glaze layer at the maximum temperature is too high compared to the viscosity of the first glaze layer at the maximum temperature. The reason for this is that the crystals precipitated due to the increase in the amount of the divalent metal oxide, particularly Z
It is suggested that friction may be acting between willemite and glass that precipitate when nO is used.

【0013】前記第二の釉薬層の成分の内、前記1価金
属酸化物のガラス成分に対する重量%が1.5%未満で
ある場合、亀甲模様が発生し、所望の釉薬面が得られな
い。これは、前記第二の釉薬層の最高温度での粘性が第
一の釉薬層の最高温度での粘性に比べて高すぎるためと
考えられる。この理由は前記1価金属酸化物量減少によ
りガラス中にSiO2を多く溶かし込むことができず、
残存した未溶解シリカとガラスとの間に摩擦が働いてい
る可能性が示唆される。
When the weight% of the monovalent metal oxide to the glass component is less than 1.5% of the components of the second glaze layer, a turtle pattern occurs and a desired glaze surface cannot be obtained. . This is probably because the viscosity of the second glaze layer at the maximum temperature is too high compared to the viscosity of the first glaze layer at the maximum temperature. The reason is that a large amount of SiO2 cannot be dissolved in the glass due to the decrease in the amount of the monovalent metal oxide,
It is suggested that friction may be acting between the remaining undissolved silica and the glass.

【0014】前記第二の釉薬層の成分の内、前記1価金
属酸化物のガラス成分に対する重量%が6.5%以上で
ある場合、斑点模様が発生し、所望の釉薬面が得られな
い。これは、前記第二の釉薬層の最高温度での粘性が第
一の釉薬層の最高温度での粘性に比べて低すぎるためと
考えられる。この理由は前記1価金属酸化物量増加によ
りガラス中にSiO2を多く溶かし込むことができるた
め、未溶解シリカが残存せずにニュートン流体としての
挙動を示してしまう可能性が示唆される。
When the weight% of the monovalent metal oxide with respect to the glass component among the components of the second glaze layer is 6.5% or more, a spot pattern is generated and a desired glaze surface cannot be obtained. . This is probably because the viscosity of the second glaze layer at the highest temperature is too low compared to the viscosity of the first glaze layer at the highest temperature. The reason for this suggests that a large amount of SiO2 can be dissolved in the glass due to the increase in the amount of the monovalent metal oxide. Therefore, it is suggested that undissolved silica does not remain and may exhibit a behavior as a Newtonian fluid.

【0015】[0015]

【発明の実施の形態】本発明は、例えば、大便器、小便
器、洗面器、手洗器等の衛生陶器に利用できる。また大
便器においては、ボール面、トラップ部、リム裏等、小
便器においては、ボール面、トラップ部、サナ等、洗面
器、手洗器においては、ボール面等の汚れの付着しやす
い一部分への適用も有効である。前記第一の釉薬層の成
分は、SiO2成分とAl2O3成分と2価金属酸化物
成分、1価金属酸化物成分及び乳濁剤を主成分とする
が、他にTiO2、V2O5等や酸化コバルト等の着色
顔料が含まれていてもよい。前記第二の釉薬層の成分
は、SiO2成分とAl2O3成分と2価金属酸化物成
分及び1価金属酸化物成分を主成分とするが他にTiO
2、V2O5等が含有されていてもよい。上記2価金属
酸化物成分には、CaO、MgO等アルカリ土類金属酸
化物、ZnO、CuO等が利用できる。上記1価金属酸
化物成分には、Na2O、K2O、Li2O等が利用で
きる。
DESCRIPTION OF THE PREFERRED EMBODIMENTS The present invention can be used for sanitary ware such as toilets, urinals, washbasins, handwashers, and the like. In the case of toilet bowls, ball surfaces, traps, rim back, etc., in the case of urinals, ball surfaces, traps, sana, etc. Application is also effective. The components of the first glaze layer are mainly composed of a SiO2 component, an Al2O3 component, a divalent metal oxide component, a monovalent metal oxide component, and an emulsifier, but may be TiO2, V2O5, cobalt oxide, or the like. May be contained. The components of the second glaze layer are mainly composed of a SiO2 component, an Al2O3 component, a divalent metal oxide component and a monovalent metal oxide component.
2, V2O5 and the like may be contained. As the divalent metal oxide component, alkaline earth metal oxides such as CaO and MgO, ZnO, CuO and the like can be used. As the monovalent metal oxide component, Na2O, K2O, Li2O, or the like can be used.

【0016】[0016]

【実施例】【Example】

【表1】 [Table 1]

【0017】[0017]

【表2】 [Table 2]

【0018】表1の組成からなる釉薬原料2Kgと水1
Kg及び球石4Kgを、容積6リットルの陶器性ポット
に入れ、レーザー回折式粒度分布計を用いた粉砕後の着
色性釉薬スラリーの粒度測定結果が、10μm以下が6
5%、50%平均粒径(D50)が6.5μm程度にな
るように、ボールミルにより粉砕を行い、着色性の第一
の釉薬スラリーを得た。
2 kg of a glaze raw material having the composition shown in Table 1 and water 1
Kg and 4 Kg of cobblestone were placed in a 6-liter pottery pot, and the particle size of the colored glaze slurry after pulverization using a laser diffraction type particle size distribution analyzer was 10 μm or less.
Pulverization was performed by a ball mill so that the 5% and 50% average particle diameters (D50) became about 6.5 μm, to obtain a first colorable glaze slurry.

【0019】これとは別に、表2の組成からなる釉薬原
料と同組成の非晶質釉薬とを、両者の合計和に対する非
晶質釉薬の割合が50〜99重量%になるように調整し
た釉薬原料2Kgと水1Kg及び球石4Kgを、容積6
リットルの陶器性ポットに入れ、レーザー回折式粒度分
布計を用いた粉砕後の透明性釉薬スラリーの粒度測定結
果が、10μm以下が67%、50%平均粒径(D5
0)が6.0μmになるように、ボールミルにより粉砕
を行い、透明性の第二の釉薬スラリー(以下と記す)
を得た。
Separately, a glaze raw material having the composition shown in Table 2 and an amorphous glaze having the same composition were adjusted so that the ratio of the amorphous glaze to the total sum of the two was 50 to 99% by weight. 2 kg of raw material for glaze, 1 kg of water and 4 kg of cobblestone are added in a volume of 6
Of the transparent glaze slurry after pulverization using a laser diffraction type particle size distribution meter in a ceramic liter of 10 liters.
Pulverization is performed by a ball mill so that 0) becomes 6.0 μm, and a transparent second glaze slurry (described below)
I got

【0020】これとは別に、表2の組成に対してNa2
O及びK2Oをそれぞれ2%添加した組成の釉薬原料と
同組成の非晶質釉薬とを、両者の合計和に対する非晶質
釉薬の割合が50〜99重量%になるように調整した釉
薬原料2Kgと水1Kg及び球石4Kgを、容積6リッ
トルの陶器性ポットに入れ、レーザー回折式粒度分布計
を用いた粉砕後の透明性釉薬スラリーの粒度測定結果
が、10μm以下が67%、50%平均粒径(D50)
が6.0μmになるように、ボールミルにより粉砕を行
い、透明性の第二の釉薬スラリー(以下と記す)を得
た。
Separately, Na2 was added to the composition shown in Table 2.
2 kg of glaze raw material obtained by adjusting a glaze raw material having a composition to which O and K2O are added by 2% each and an amorphous glaze having the same composition so that the ratio of the amorphous glaze to the total sum of the two is 50 to 99% by weight. And 1 kg of water and 4 kg of cobblestone are placed in a 6 liter pottery pot, and the particle size of the transparent glaze slurry after pulverization using a laser diffraction type particle size distribution analyzer is 67% for 10 μm or less and 50% average. Particle size (D50)
Was crushed by a ball mill to obtain a transparent second glaze slurry (hereinafter described).

【0021】これとは別に、表2の組成に対してSiO
2を5%添加した組成の釉薬原料と同組成の非晶質釉薬
とを、両者の合計和に対する非晶質釉薬の割合が50〜
99重量%になるように調整した釉薬原料2Kgと水1
Kg及び球石4Kgを、容積6リットルの陶器性ポット
に入れ、レーザー回折式粒度分布計を用いた粉砕後の透
明性釉薬スラリーの粒度測定結果が、10μm以下が6
7%、50%平均粒径(D50)が6.0μmになるよ
うに、ボールミルにより粉砕を行い、透明性の第二の釉
薬スラリー(以下と記す)を得た。
Separately, for the compositions shown in Table 2, SiO 2
The ratio of the amorphous glaze to the total sum of the glaze raw material having the composition of 2% and the amorphous glaze having the same composition is 50 to 50%.
2 kg of glaze raw material and water 1 adjusted to 99% by weight
Kg and 4 Kg of cobblestone are put into a 6-liter pottery pot, and the particle size of the transparent glaze slurry after pulverization using a laser diffraction type particle size distribution analyzer is 6 μm when the particle size is 10 μm or less.
Pulverization was performed by a ball mill so that the 7% and 50% average particle diameters (D50) became 6.0 μm, to obtain a transparent second glaze slurry (described below).

【0022】次に、珪砂、長石、粘土等を原料として調
製した衛生陶器素地泥漿を用いて、70×150mm板
状試験片および大便器を作製し、上記の如くして得られ
た着色性の第一の釉薬スラリーを、板状試験片にスプレ
ーコーティング法により塗布し、更にその上に透明性の
第二の釉薬スラリー(〜)をスプレーコーティング
法により塗布を行った。その後、1100〜1200℃
で焼成することにより試料(〜)を得た。
Next, a 70 × 150 mm plate-shaped test piece and a toilet bowl were prepared using a slurry of sanitary ware body prepared from silica sand, feldspar, clay and the like, and the coloring property obtained as described above was obtained. The first glaze slurry was applied to a plate-shaped test piece by a spray coating method, and a transparent second glaze slurry (〜) was further applied thereon by a spray coating method. Then, 1100-1200 ° C
The sample (-) was obtained by baking with.

【0023】得られた板状試験片について、釉薬表面粗
さ(Ra)の測定、および外観欠点の確認を行った。表
面粗さは触針式表面粗さ測定器(JIS−B0651)
を用い、中心線表面粗さ(Ra)を測定した。外観欠点
は、目視により確認を行った。
The surface roughness (Ra) of the glaze was measured and the appearance defect was confirmed for the obtained plate-shaped test piece. Surface roughness is measured by a stylus type surface roughness meter (JIS-B0651)
Was used to measure the center line surface roughness (Ra). The appearance defect was confirmed visually.

【0024】各々の結果は表3に示したように、透明性
の第二の釉薬の組成に関してSiO2が増加すると亀甲
模様が発生し、外観での製造上の欠点が発生し始める。
The results, as shown in Table 3, show that as SiO2 increases with respect to the composition of the second transparent glaze, a turtle pattern starts to appear and a manufacturing defect in appearance begins to occur.

【0025】一方、透明性の第二の釉薬の組成に関して
1価金属酸化物が増加すると斑点模様が発生し、外観で
の製造上の欠点が発生し始める。更に大便器についても
同様の確認を行い、試験片と同傾向であることの確認を
行った。
On the other hand, with respect to the composition of the transparent second glaze, when the monovalent metal oxide is increased, a spot pattern is generated, and a manufacturing defect in appearance starts to occur. In addition, the same check was performed for the toilet bowl, and it was confirmed that the tendency was the same as that of the test piece.

【0026】[0026]

【表3】 [Table 3]

【0027】[0027]

【発明の効果】本発明によれば、製造上のばらつきに拘
らず表面粗さ(Ra)を0.07m未満に維持すること
ができ、また外観不良等の製造上の欠点を最小限に抑え
た衛生陶器を提供することが可能となる。
According to the present invention, the surface roughness (Ra) can be maintained at less than 0.07 m irrespective of manufacturing variations, and manufacturing defects such as poor appearance are minimized. It becomes possible to provide sanitary ware that has been improved.

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

【図1】本発明の実施例を示す図である。FIG. 1 is a diagram showing an embodiment of the present invention.

【符号の説明】[Explanation of symbols]

1…衛生陶器素地 2…第一の釉薬層(着色性の釉薬層) 3…第二の釉薬層(透明性の釉薬層) 1. Sanitary ware base 2. First glaze layer (colorable glaze layer) 3. Second glaze layer (transparent glaze layer)

───────────────────────────────────────────────────── フロントページの続き (72)発明者 山田 茂幸 福岡県北九州市小倉北区中島2丁目1番1 号 東陶機器株式会社内 (72)発明者 上野 徹 福岡県北九州市小倉北区中島2丁目1番1 号 東陶機器株式会社内 (72)発明者 高田 宏行 福岡県北九州市小倉北区中島2丁目1番1 号 東陶機器株式会社内 (72)発明者 松本 幸成 福岡県北九州市小倉北区中島2丁目1番1 号 東陶機器株式会社内 (72)発明者 須田 稔光 福岡県北九州市小倉北区中島2丁目1番1 号 東陶機器株式会社内 (72)発明者 川上 克博 福岡県北九州市小倉北区中島2丁目1番1 号 東陶機器株式会社内 ──────────────────────────────────────────────────続 き Continuing from the front page (72) Inventor Shigeyuki Yamada 2-1-1 Nakajima, Kokurakita-ku, Kitakyushu-shi, Fukuoka Touchi Kiki Co., Ltd. (72) Inventor Toru Ueno 2 Nakajima, Kokurakita-ku, Kitakyushu-shi, Fukuoka 1-1-1 Totoki Kiki Co., Ltd. (72) Inventor Hiroyuki Takada 2-1-1 Nakajima, Kokurakita-ku, Kitakyushu-shi, Fukuoka Tochiki Kiki Co., Ltd. (72) Inventor Yukinari Matsumoto Kokura, Kitakyushu-shi, Fukuoka 2-11-1, Nakajima, Kita-ku, Totoki Equipment Co., Ltd. (72) Inventor Minoru Suda 2-1-1, Nakajima, Kokurakita-ku, Kitakyushu-shi, Fukuoka Totoki Equipment Co., Ltd. (72) Katsuhiro Kawakami, Inventor 2-1, 1-1 Nakajima, Kokurakita-ku, Kitakyushu-shi, Fukuoka

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 陶器素地表面に着色顔料を含む第一の釉
薬層が形成されており、その上に着色顔料を含まない第
二の釉薬層が形成されている衛生陶器であって、第一の
釉薬層の成分がSiO2、Al2O3、2価金属酸化
物、1価金属酸化物及び乳濁剤から成っており、前記S
iO2のガラス成分に対する重量%が55〜80%であ
り、前記Al2O3のガラス成分に対する重量%が5〜
13%であり、前記2価金属酸化物のガラス成分に対す
る重量%が10〜25%であり、前記1価金属酸化物の
ガラス成分に対する重量%が1.5〜6.5%であり、且
つ乳濁剤のガラス成分に対する重量%が0.1〜15%で
あり、前記第二の釉薬層の成分がSiO2、Al2O
3、2価金属酸化物及び1価金属酸化物から成ってお
り、前記SiO2のガラス成分に対する重量%が52〜
76%であり、前記Al2O3のガラス成分に対する重
量%が6〜14%であり、前記2価金属酸化物のガラス
成分に対する重量%が13〜28%であり、前記1価金
属酸化物のガラス成分に対する重量%が1.5〜6.5%
であることを特徴とする衛生陶器。
1. A sanitary ware having a first glaze layer containing a color pigment formed on a surface of a pottery substrate, and a second glaze layer not containing a color pigment formed thereon. The glaze layer comprises SiO2, Al2O3, a divalent metal oxide, a monovalent metal oxide, and an emulsifier.
The weight percentage of iO2 to the glass component is 55 to 80%, and the weight percentage of Al2O3 to the glass component is 5 to 80%.
13%, the weight% of the divalent metal oxide with respect to the glass component is 10 to 25%, the weight% of the monovalent metal oxide with respect to the glass component is 1.5 to 6.5%, and The weight% of the emulsifier with respect to the glass component is 0.1 to 15%, and the component of the second glaze layer is SiO2, Al2O.
It is composed of a trivalent metal oxide and a monovalent metal oxide, and the weight percentage of the SiO2 to the glass component is 52 to 50%.
76%, the weight% of the Al2O3 with respect to the glass component is 6-14%, the weight% of the divalent metal oxide with respect to the glass component is 13-28%, and the glass component of the monovalent metal oxide 1.5% to 6.5% by weight
A sanitary ware characterized by being.
【請求項2】 前記第二の釉薬層表面の表面粗さが0.
07μm未満であることを特徴とする請求項1に記載の
衛生陶器。
2. The surface of the second glaze layer has a surface roughness of 0.5.
The sanitary ware according to claim 1, wherein the sanitary ware is less than 07 µm.
JP12788399A 1999-05-10 1999-05-10 Sanitary ware Expired - Fee Related JP3783466B2 (en)

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JP3783466B2 JP3783466B2 (en) 2006-06-07

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Country Link
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000302579A (en) * 1999-04-19 2000-10-31 Toto Ltd Production of sanitary ware

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01100084A (en) * 1987-10-13 1989-04-18 Nippon Steel Corp Production of spray-coated tile
JPH04187580A (en) * 1990-11-19 1992-07-06 Miyawaki Gureizu Kogyo Kk Production of ceramic product using colored glazing grain
JPH05262581A (en) * 1992-03-16 1993-10-12 Toto Ltd Production of decorative ceramic
JPH05270859A (en) * 1991-04-17 1993-10-19 Cookson Group Plc Glaze composition and glazing method
JPH06321667A (en) * 1993-05-14 1994-11-22 Inax Corp Production of in-kiln modified tile
JP2000226278A (en) * 1998-11-30 2000-08-15 Toto Ltd Earthenware and its production
JP2000272988A (en) * 1999-03-24 2000-10-03 Toto Ltd Sanitary ware
JP2001058865A (en) * 1998-05-27 2001-03-06 Toto Ltd Sanitary earthenware and production thereof

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01100084A (en) * 1987-10-13 1989-04-18 Nippon Steel Corp Production of spray-coated tile
JPH04187580A (en) * 1990-11-19 1992-07-06 Miyawaki Gureizu Kogyo Kk Production of ceramic product using colored glazing grain
JPH05270859A (en) * 1991-04-17 1993-10-19 Cookson Group Plc Glaze composition and glazing method
JPH05262581A (en) * 1992-03-16 1993-10-12 Toto Ltd Production of decorative ceramic
JPH06321667A (en) * 1993-05-14 1994-11-22 Inax Corp Production of in-kiln modified tile
JP2001058865A (en) * 1998-05-27 2001-03-06 Toto Ltd Sanitary earthenware and production thereof
JP3339640B2 (en) * 1998-05-27 2002-10-28 東陶機器株式会社 Sanitary ware and manufacturing method thereof
JP2000226278A (en) * 1998-11-30 2000-08-15 Toto Ltd Earthenware and its production
JP2000272988A (en) * 1999-03-24 2000-10-03 Toto Ltd Sanitary ware

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2000302579A (en) * 1999-04-19 2000-10-31 Toto Ltd Production of sanitary ware

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