CN100450976C - Method for preparing positioning iron red crystal glaze - Google Patents

Method for preparing positioning iron red crystal glaze Download PDF

Info

Publication number
CN100450976C
CN100450976C CNB2007100183854A CN200710018385A CN100450976C CN 100450976 C CN100450976 C CN 100450976C CN B2007100183854 A CNB2007100183854 A CN B2007100183854A CN 200710018385 A CN200710018385 A CN 200710018385A CN 100450976 C CN100450976 C CN 100450976C
Authority
CN
China
Prior art keywords
glaze
preparation
nucleus agent
ferric oxide
kaolin
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
CNB2007100183854A
Other languages
Chinese (zh)
Other versions
CN101121611A (en
Inventor
朱建锋
王芬
罗宏杰
杨海波
林营
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.)
Shaanxi University of Science and Technology
Original Assignee
Shaanxi University of Science and Technology
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 Shaanxi University of Science and Technology filed Critical Shaanxi University of Science and Technology
Priority to CNB2007100183854A priority Critical patent/CN100450976C/en
Publication of CN101121611A publication Critical patent/CN101121611A/en
Application granted granted Critical
Publication of CN100450976C publication Critical patent/CN100450976C/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Compositions Of Oxide Ceramics (AREA)
  • Dental Preparations (AREA)

Abstract

The present invention discloses a preparation method for positioning ferreous crystal; the preparation of the base glaze is that: potassic feldspar, quartz, kaoline, ocher, steatite, limestone and bone ash are mixed with ferric oxide for grilling; the proportion of the glaze slurry is 1.6-1.7 g/cm3; the preparation method of the crystal core is that: kaoline is mixed with ferric oxide for grilling and calcining and cooling to become grain powder; and then crystal core is pre-buried in the position for the blank body to form the crystal flower; the size Phi of the preburied hole is about 1mm; the quantity and distribution are adjusted according to the actual requirement; the base glaze is put on the ceramic blank body preburied with crystal core evenly; the thickness of the glaze level is controlled on 0.7-1.0mm; the semi finished product of the ceramic glaze is baked to the maximum temperature with oxidation blaze, and then is cooled into the room temperature. The present invention uses the common ceramic raw material and the positioning crystal measure to produce the positioning ferreous crystal glaze, which solves the shortcoming that the size and the distribution for the ferreous crystal flower is hard to be controlled; the method is a stable preparation method with simple process technical, wide baking temperature range, good stability, without needing middle temperature heat preservation; the produce cost is much lower.

Description

A kind of preparation method of positioning iron red crystal glaze
Technical field
The invention belongs to the stupalith field, be specifically related to a kind of preparation method of positioning iron red crystal glaze.
Background technology
Along with growth in the living standard, people are also more and more higher to the demand grade of decorative ceramics, very big variation has taken place in modern's aesthetic consciousness, and people no longer appreciate those complicated numerous and jumbled works, but are more attracted by extremely uncomplicated, the simple and unadorned and generous form of the original art of the mankind.
To be crystalline glaze in the Song dynasty begin to burn iron makes, and the tea set that forms a kind of characteristic decorates, and famous have kinds such as oil droplet, the writing brush made of rabbit's hair, francolin spot at that time, is the earliest one of crystalline glaze product in the world.Iron red crystal glaze (iron oxide red fancy glaze) is the category of crystalline glaze as iron, its glaze is the pea size on the umbrinaceous background color, the discrete red crystallization of circle, make whole goods present unique beautiful outward appearance, just as a bunch bunch red plum that bursts forth, rich and gaudy and do not show poor taste, have on the high artistry to be worth.Its appearance once caused the attention on domestic and international ceramic boundary.But because its crystalline range is narrower; Firing condition harshness, and often be difficult for again controlling artificially that crystalline distributes and quantity in the glaze makes the stability and the repeated extreme difference of this series products; Brought difficulty to commercialization production, so that this series products can only rest on the position of showpiece for a long time.
Summary of the invention
The objective of the invention is to overcome the deficiencies in the prior art, provide a kind of preparation technology simple, enlarged the maturing range of iron red crystal glaze, improved its stability and repeated, easy realization of industrialization is produced, and the preparation method of the lower positioning iron red crystal glaze of manufacturing cost.
For achieving the above object, the technical solution used in the present invention is: by mass percentage with the potassium felspar sand of 40-45%, the quartz of 10-15%, the kaolin of 5-8%, the loess of 5-8%, the talcum of 8-10%, the Wingdale of 5-6%, the bone ash of 12-15% and 7-12% ferric oxide mix, and are finely ground to 250 orders, glaze slip proportion 1.6-1.7g/cm 3
2) nucleus agent preparation method: by mass percentage with the ferric oxide mixing of the kaolin of 30-70% and 30-70%, ball milling, 1270-1300 ℃ of calcining, be ground into the particle about 1mm after the cooling;
3) the nucleus agent is embedded in base substrate and need forms on the crystalline position, pre-buried via hole exists About, the quantity and the adjustment voluntarily as required that distributes;
4) parent glaze is evenly bestowed on the ceramic body that is embedded with the nucleus agent, the glaze layer thickness is controlled at 0.7-1.0mm and obtains work in-process;
5) work in-process are burnt till with oxydizing flame under 1270 ℃-1300 ℃, be incubated and naturally cool to room temperature after 10-30 minute and get final product.
The present invention utilizes conventional ceramic raw material, and utilization location crystallization means have made positioning iron red crystal glaze, has solved the size and the distribution of the brilliant flower of iron oxide red, realized stable preparation method, because technology is simple, wide, the good stability of firing range, temperature insulation in need not, production cost is lower.
Embodiment
Embodiment 1: by mass percentage with 40% potassium felspar sand, and 15% quartz, 5% kaolin, 5% loess, 10% talcum, 5% Wingdale, 13% bone ash and 7% ferric oxide mix, and are finely ground to 250 orders, glaze slip proportion 1.6g/cm 3Nucleus agent preparation method: by mass percentage with the ferric oxide mixing of 30% kaolin and 70%, ball milling, 1270 ℃ of calcinings, be ground into the particle about 1mm after the cooling; The nucleus agent is embedded in base substrate need forms on the crystalline position, pre-buried via hole exists usually
Figure C20071001838500062
Figure C20071001838500063
About, the quantity and the adjustment voluntarily as required that distributes; Parent glaze is evenly bestowed on the ceramic body that is embedded with the nucleus agent, and the glaze layer thickness is controlled at 0.7mm and obtains work in-process; Work in-process are burnt till with oxydizing flame under 1270 ℃, be incubated and naturally cool to room temperature after 20 minutes and get final product.
Embodiment 2: by mass percentage with 45% potassium felspar sand, and 10% quartz, 6% kaolin, 6% loess, 8% talcum, 5% Wingdale, 12% bone ash and 8% ferric oxide mix, and are finely ground to 250 orders, glaze slip proportion 1.7g/cm 3Nucleus agent preparation method: by mass percentage with the ferric oxide mixing of 50% kaolin and 50%, ball milling, 1290 ℃ of calcinings, be ground into the particle about 1mm after the cooling; The nucleus agent is embedded in base substrate need forms on the crystalline position, pre-buried via hole exists usually
Figure C20071001838500071
About, the quantity and the adjustment voluntarily as required that distributes; Parent glaze is evenly bestowed on the ceramic body that is embedded with the nucleus agent, and the glaze layer thickness is controlled at 0.9mm and obtains work in-process; Work in-process are burnt till with oxydizing flame under 1290 ℃, be incubated and naturally cool to room temperature after 30 minutes and get final product.
Embodiment 3: by mass percentage with 42% potassium felspar sand, and 12% quartz, 8% kaolin, 5% loess, 8% talcum, 6% Wingdale, 12% bone ash and 7% ferric oxide mix, and are finely ground to 250 orders, glaze slip proportion 1.7g/cm 3Nucleus agent preparation method: by mass percentage with the ferric oxide mixing of 70% kaolin and 30%, ball milling, 1280 ℃ of calcinings, be ground into the particle about 1mm after the cooling; The nucleus agent is embedded in base substrate need forms on the crystalline position, pre-buried via hole exists usually
Figure C20071001838500073
Figure C20071001838500074
About, the quantity and the adjustment voluntarily as required that distributes; Parent glaze is evenly bestowed on the ceramic body that is embedded with the nucleus agent, and the glaze layer thickness is controlled at 0.8mm and obtains work in-process; Work in-process are burnt till with oxydizing flame under 1280 ℃, be incubated and naturally cool to room temperature after 10 minutes and get final product.
Embodiment 4: by mass percentage with 40% potassium felspar sand, and 10% quartz, 5% kaolin, 8% loess, 8% talcum, 5% Wingdale, 15% bone ash and 9% ferric oxide mix, and are finely ground to 250 orders, glaze slip proportion 1.6g/cm 3Nucleus agent preparation method: by mass percentage with the ferric oxide mixing of 40% kaolin and 60%, ball milling, 1300 ℃ of calcinings, be ground into the particle about 1mm after the cooling; The nucleus agent is embedded in base substrate need forms on the crystalline position, pre-buried via hole exists usually
Figure C20071001838500076
About, the quantity and the adjustment voluntarily as required that distributes; Parent glaze is evenly bestowed on the ceramic body that is embedded with the nucleus agent, and the glaze layer thickness is controlled at 1.0mm and obtains work in-process; Work in-process are burnt till with oxydizing flame under 1300 ℃, be incubated and naturally cool to room temperature after 15 minutes and get final product.
Embodiment 5: by mass percentage with 40% potassium felspar sand, and 10% quartz, 5% kaolin, 6% loess, 9% talcum, 6% Wingdale, 12% bone ash and 12% ferric oxide mix, and are finely ground to 250 orders, glaze slip proportion 1.7g/cm 3Nucleus agent preparation method: by mass percentage with the ferric oxide mixing of 60% kaolin and 40%, ball milling, 1280 ℃ of calcinings, be ground into the particle about 1mm after the cooling; The nucleus agent is embedded in base substrate need forms on the crystalline position, pre-buried via hole exists usually
Figure C20071001838500082
About, the quantity and the adjustment voluntarily as required that distributes; Parent glaze is evenly bestowed on the ceramic body that is embedded with the nucleus agent, and the glaze layer thickness is controlled at 1.0mm and obtains work in-process; Work in-process are burnt till with oxydizing flame under 1280 ℃, be incubated and naturally cool to room temperature after 25 minutes and get final product.

Claims (6)

1, a kind of preparation method of positioning iron red crystal glaze is characterized in that:
1) preparation of parent glaze: by mass percentage with the potassium felspar sand of 40-45%, the quartz of 10-15%, the kaolin of 5-8%, the loess of 5-8%, the talcum of 8-10%, the Wingdale of 5-6%, the bone ash of 12-15% and 7-12% ferric oxide mix, and are finely ground to 250 orders, glaze slip proportion 1.6-1.7g/cm 3
2) nucleus agent preparation method: by mass percentage with the ferric oxide mixing of the kaolin of 30-70% and 30-70%, ball milling, 1270-1300 ℃ of calcining, be ground into the particle about 1mm after the cooling;
3) the nucleus agent is embedded in base substrate and need forms on the crystalline position, pre-buried via hole exists
Figure C2007100183850002C1
About, the quantity and the adjustment voluntarily as required that distributes;
4) parent glaze is evenly bestowed on the ceramic body that is embedded with the nucleus agent, the glaze layer thickness is controlled at 0.7-1.0mm, thereby obtains work in-process;
5) work in-process are burnt till with oxydizing flame under 1270 ℃-1300 ℃, be incubated and naturally cool to room temperature after 10-30 minute and get final product.
2, the preparation method of positioning iron red crystal glaze according to claim 1, it is characterized in that: by mass percentage with 40% potassium felspar sand, 15% quartz, 5% kaolin, 5% loess, 10% talcum, 5% Wingdale, 13% bone ash and 7% ferric oxide mix, and are finely ground to 250 orders, glaze slip proportion 1.6g/cm 3Nucleus agent preparation method: by mass percentage with the ferric oxide mixing of 30% kaolin and 70%, ball milling, 1270 ℃ of calcinings, be ground into the particle about 1mm after the cooling; The nucleus agent is embedded in base substrate need forms on the crystalline position, pre-buried via hole exists
Figure C2007100183850002C2
About, the quantity and the adjustment voluntarily as required that distributes; Parent glaze is evenly bestowed on the ceramic body that is embedded with the nucleus agent, and the glaze layer thickness is controlled at 0.7mm and obtains work in-process; Work in-process are burnt till with oxydizing flame under 1270 ℃, be incubated and naturally cool to room temperature after 20 minutes and get final product.
3, the preparation method of positioning iron red crystal glaze according to claim 1, it is characterized in that: by mass percentage with 45% potassium felspar sand, 10% quartz, 6% kaolin, 6% loess, 8% talcum, 5% Wingdale, 12% bone ash and 8% ferric oxide mix, and are finely ground to 250 orders, glaze slip proportion 1.7g/cm 3Nucleus agent preparation method: by mass percentage with the ferric oxide mixing of 50% kaolin and 50%, ball milling, 1290 ℃ of calcinings, be ground into the particle about 1mm after the cooling; The nucleus agent is embedded in base substrate need forms on the crystalline position, pre-buried via hole exists
Figure C2007100183850003C1
About, the quantity and the adjustment voluntarily as required that distributes; Parent glaze is evenly bestowed on the ceramic body that is embedded with the nucleus agent, and the glaze layer thickness is controlled at 0.9mm and obtains work in-process; Work in-process are burnt till with oxydizing flame under 1290 ℃, be incubated and naturally cool to room temperature after 30 minutes and get final product.
4, the preparation method of positioning iron red crystal glaze according to claim 1, it is characterized in that: at first by mass percentage with 42% potassium felspar sand, 12% quartz, 8% kaolin, 5% loess, 8% talcum, 6% Wingdale, 12% bone ash and 7% ferric oxide mix, and are finely ground to 250 orders, then glaze slip proportion 1.7g/cm 3Soak glaze; Nucleus agent preparation method: by mass percentage with the ferric oxide mixing of 70% kaolin and 30%, ball milling, 1280 ℃ of calcinings, be ground into the particle about 1mm after the cooling; The nucleus agent is embedded in base substrate need forms on the crystalline position, pre-buried via hole exists
Figure C2007100183850003C2
About, the quantity and the adjustment voluntarily as required that distributes; Parent glaze is evenly bestowed on the ceramic body that is embedded with the nucleus agent, and the glaze layer thickness is controlled at 0.8mm and obtains work in-process; Work in-process are burnt till with oxydizing flame under 1280 ℃, be incubated and naturally cool to room temperature after 10 minutes and get final product.
5, the preparation method of positioning iron red crystal glaze according to claim 1, it is characterized in that: at first by mass percentage with 40% potassium felspar sand, 10% quartz, 5% kaolin, 8% loess, 8% talcum, 5% Wingdale, 15% bone ash and 9% ferric oxide mix, and are finely ground to 250 orders, then glaze slip proportion 1.6g/cm 3Soak glaze; Nucleus agent preparation method: by mass percentage with the ferric oxide mixing of 40% kaolin and 60%, ball milling, 1300 ℃ of calcinings, be ground into the particle about 1mm after the cooling; The nucleus agent is embedded in base substrate need forms on the crystalline position, pre-buried via hole exists
Figure C2007100183850004C1
About, the quantity and the adjustment voluntarily as required that distributes; Parent glaze is evenly bestowed on the ceramic body that is embedded with the nucleus agent, and the glaze layer thickness is controlled at 1.0mm and obtains work in-process; Work in-process are burnt till with oxydizing flame under 1300 ℃, be incubated and naturally cool to room temperature after 15 minutes and get final product.
6, the preparation method of positioning iron red crystal glaze according to claim 1, it is characterized in that: at first by mass percentage with 40% potassium felspar sand, 10% quartz, 5% kaolin, 6% loess, 9% talcum, 6% Wingdale, 12% bone ash and 12% ferric oxide mix, and are finely ground to 250 orders, then glaze slip proportion 1.7g/cm 3Soak glaze; Nucleus agent preparation method: by mass percentage with the ferric oxide mixing of 60% kaolin and 40%, ball milling, 1280 ℃ of calcinings, be ground into the particle about 1mm after the cooling; The nucleus agent is embedded in base substrate need forms on the crystalline position, pre-buried via hole exists About, the quantity and the adjustment voluntarily as required that distributes; Parent glaze is evenly bestowed on the ceramic body that is embedded with the nucleus agent, and the glaze layer thickness is controlled at 1.0mm and obtains work in-process; Work in-process are burnt till with oxydizing flame under 1280 ℃, be incubated and naturally cool to room temperature after 25 minutes and get final product.
CNB2007100183854A 2007-07-31 2007-07-31 Method for preparing positioning iron red crystal glaze Expired - Fee Related CN100450976C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB2007100183854A CN100450976C (en) 2007-07-31 2007-07-31 Method for preparing positioning iron red crystal glaze

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB2007100183854A CN100450976C (en) 2007-07-31 2007-07-31 Method for preparing positioning iron red crystal glaze

Publications (2)

Publication Number Publication Date
CN101121611A CN101121611A (en) 2008-02-13
CN100450976C true CN100450976C (en) 2009-01-14

Family

ID=39084136

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB2007100183854A Expired - Fee Related CN100450976C (en) 2007-07-31 2007-07-31 Method for preparing positioning iron red crystal glaze

Country Status (1)

Country Link
CN (1) CN100450976C (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101624297B (en) * 2009-08-07 2011-11-09 陕西科技大学 Preparation method for tea dust temmoku glaze
CN102173869B (en) * 2011-01-19 2013-02-27 江苏高淳陶瓷股份有限公司 Preparation method of non-ferrous tea dust crystalline glaze
CN104446659A (en) * 2014-12-01 2015-03-25 王桂忠 Iron oxide oil-drop transmutation glaze
CN105218166A (en) * 2015-10-23 2016-01-06 张昭 Self-cleaning mirror face ceramics glaze of hydrophobic and preparation method thereof
CN105693091B (en) * 2016-01-20 2018-05-15 福建省德化县鸿芳陶瓷有限公司 Sapporo color ceramic and its Sapporo color ceramic preparation process
CN107619188A (en) * 2017-10-25 2018-01-23 西安文理学院 A kind of ceramic glaze and preparation method thereof
CN109627051A (en) * 2018-12-30 2019-04-16 鲁山县段店花瓷非物质文化遗产开发有限公司 The production method of tea set
CN110510989A (en) * 2019-07-06 2019-11-29 福建省乐普陶板制造有限公司 A kind of crystalline glaze ceramic plate and preparation method thereof
CN113860924B (en) * 2021-09-28 2023-05-02 福建省德化博龙陶瓷有限公司 Under-glaze green thorn over-glaze safflower ceramic and preparation method thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1769245A (en) * 2005-09-08 2006-05-10 陕西科技大学 Oil drop glaze preparation method
CN1887809A (en) * 2006-07-24 2007-01-03 胡天霏 Bright red underglaze color, overglaze and their prepn process

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1769245A (en) * 2005-09-08 2006-05-10 陕西科技大学 Oil drop glaze preparation method
CN1887809A (en) * 2006-07-24 2007-01-03 胡天霏 Bright red underglaze color, overglaze and their prepn process

Also Published As

Publication number Publication date
CN101121611A (en) 2008-02-13

Similar Documents

Publication Publication Date Title
CN100450976C (en) Method for preparing positioning iron red crystal glaze
CN104529548B (en) A kind of erythema crystalline glaze and adopt the ceramic preparation of this glaze
CN102173869B (en) Preparation method of non-ferrous tea dust crystalline glaze
CN101058476B (en) Antiseep glaze material and glair for Ruyao kiln package container and preparing method thereof
CN104030733B (en) Official's Song bluish white brother's kiln porcelain and preparation method thereof
CN105693207B (en) A kind of preparation method of tea dust artistic porcelain
CN101624297B (en) Preparation method for tea dust temmoku glaze
CN104016661B (en) Preparing method of bone art porcelain
CN102173873B (en) Transmutation glaze material and glazing process
CN104817343A (en) Ru porcelain tea-dust glaze and preparation technology thereof
CN101269947A (en) Celadon cracked-ice pattern tire bone and glaze material, production method for products produced thereof
CN102173875B (en) Preparation method of B2O3-TiO2 series fambe ceramic crystalline glaze
CN104860652B (en) A kind of firing builds the method that water purple is made pottery
CN101993238A (en) Silver jade ceramics and preparation method thereof
CN101768017A (en) Lavender grey glaze and manufacture method of products thereof
CN105272144B (en) A kind of intermediate sintering temperature china and preparation method thereof
CN105601110B (en) Black silver drop reduction furnace transmutation glaze and the black silver drop prepared with it restore transmutation glazed pottery ceramic products and preparation method
CN103833329A (en) Preparation method of reinforced bone china and product prepared therefrom
CN103183526A (en) Rust glaze and method for making product thereof
CN111995360A (en) Manufacturing process of squama manis oil drop jian cup
CN102515702A (en) Antique art ceramic
CN101857369A (en) Ancient submetallic glaze and preparation method thereof
CN107352798B (en) Iron oxide red fancy glaze and preparation method thereof
CN101935233B (en) Low-temperature glaze with silver white metal luster and preparation method thereof
CN103922805B (en) Silver rib puts down making method and the flat de-secret colour ware device of obtained silver-colored rib of de-secret colour ware device

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20090114

Termination date: 20110731