CN1318338C - Colour glass brown colouring pigment and its preparing process - Google Patents
Colour glass brown colouring pigment and its preparing process Download PDFInfo
- Publication number
- CN1318338C CN1318338C CNB2004100235380A CN200410023538A CN1318338C CN 1318338 C CN1318338 C CN 1318338C CN B2004100235380 A CNB2004100235380 A CN B2004100235380A CN 200410023538 A CN200410023538 A CN 200410023538A CN 1318338 C CN1318338 C CN 1318338C
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- CN
- China
- Prior art keywords
- coloring agent
- preparation
- preparing
- pigment
- brown
- Prior art date
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Abstract
The present invention relates to a brown coloring agent for color glass and a preparing technique thereof. The granular brown coloring agent for color glass is obtained by the following technical processes of adopting the formula of plumbum and boron, coloring nickel, cadmium and iron, adding zinc and lithium in the formula for coloring, preparing a fluxing agent, preparing glaze melting powder, preparing coloring matters, preparing a coloring agent, etc. The novel coloring agent of the present invention has the advantages of stable product quantity and convenient use, and can greatly reduce the production cost and replace import products. The effect of the novel coloring agent is superior to that of a similar coloring agent. In addition, the brown coloring agent of the present overcomes the defects that color channels and gas bubbles are easily generated by the coloring agent in the same type, and the effects of the brown coloring agent of the present invention are superior to that of the coloring agent in the same type.
Description
Technical field
The present invention relates to a kind of glass colorant compounds process for production thereof.
Background technology
Late 1960s, coloured glass begins to occur abroad, China began one's study the seventies, originally be in the road, to add Powdered pigment, dye melts is after stirring action, make itself and parent glass be mixed into the material of homogeneous, through the homogenizing postforming, yet this coloured glass is had to limited popularization.The first, when in glass metal, adding tinting material, can produce many difficulties, the second, glass metal is carried out second-heating detrimentally affect, and subject matter is reboil bubble to occur.U.S.'s import particulate state tinting material is used in the back, and this tinting material external product generally adopts chromium painted, though improvement is arranged, but still have unstable product quality, defectives such as look road, bubble, color lump very easily appear, and the product import, cost an arm and a leg, be badly in need of substitute products.
Summary of the invention
Cost an arm and a leg in order to overcome prior art, unstable product quality, effect is undesirable, defectives such as look road, bubble, color lump very easily occur, the invention provides a kind of new coloured glass tinting material and production technique.
New coloured glass brown colouring additive provided by the present invention adopts plumbous boron prescription, and nickel, cadmium, iron are painted, and add zinc, lithium composition in prescription, and its chemical ingredients is as follows: SiO
225-30%; Al
2O
33-6%; PbO35-40%; B
2O
35-8%; R
2O10-20%; Ni
2O3-7%; CdS2-4%; ZnO10-12%; Se1-3%; Fe
2O
30.5-1%.
Above-mentioned compound can prepare by following method.
(a) preparation of fusing assistant: the fusing assistant proportioning raw materials is SiO
230-35%; Al
2O
36-10%;
CaO0.5-2%;MgO0.2-1%;PbO45-50%;B
2O
34-8%;K
2O+Na
2O10-15%。
(b) preparation of melted glaze powder: fusing assistant is heated in crucible 1100-1200 ℃ by above-mentioned chemical constitution batching back and is founded, soak 40-60min, and through shrend, ball milling, drying, sieving obtains melted glaze powder.
(c) preparation of pigment, it is toner that bronzing agent adopts nickel, cadmium, iron, its composition of raw materials: Ni
2O20-30%; CdS8-12%; Fe
2O
31-2%; ZnO20-30%; Li
2CO
316-20%; Se2-4%; B
2O
36-10%.Borax is earlier soluble in water, and powder adds behind all the other raw material blendings, mixes oven dry thoroughly, and ball milling sieves, and obtains pigment
(d) preparation of tinting material: fusing assistant and pigment by fusion in crucible after 2: 1 mixed, are injected the cold water hardening crack then, and dry back fragmentation is sieved, the brown particle agent.
Embodiment
The invention will be further described below in conjunction with embodiment
The preparation of the coloured glass brown colouring additive of indication of the present invention realizes by following processing method.
One, the preparation of fusing assistant
In order to adapt to the processing temperature of expecting the road and the chemical constitution and the chemical property of glass basestocks.Reduce PbO, B
2O
3Deng the volatile quantity of raw material, fusing assistant is selected following raw materials according proportioning: SiO for use
230-35%; Al
2O
36-10%; CaO0.5-2%; MgO0.2-1%; PbO45-50%; B
2O
34-8%; K
2O+Na
2O10-15%.
Two, the preparation of melted glaze powder
Fusing assistant is formed the batching back by its said ratio and found into vitreum in crucible, and glass melting temperature is about 1180 ℃, and top temperature keeps 50min, pours into then and carries out shrend in the water, the molten glaze ball milling after the shrend 28 hours.80 mesh sieves are crossed in dry back, obtain powdered frit.
Three, the preparation of pigment
It is toner that brown colouring additive adopts nickel, cadmium, iron, its pigment raw material proportioning: Ni
2O20-30%; CdS8-12%; Fe
2O
31-2%; ZnO20-30%; Li
2CO
316-20%; Se2-4%; B
2O
36-10%.The raw materials used chemical pure raw material that all adopts of pigment requires steady quality, and borax is earlier soluble in water, and powder behind all the other raw material blendings is added, mixes thoroughly oven dry, and ball milling was crossed 280 mesh sieves about 25 hours, obtained pigment.
Four, the preparation of tinting material
Fusing assistant and pigment by fusion in crucible after 2: 1 mixed, are injected the cold water hardening crack then, broken 4 orders of crossing in dry back, 10 mesh sieves, intermediate particle is the particulate state brown colouring additive, its main chemical compositions: SiO
225-30%; Al
2O
33-6%; PbO35-40%; B
2O
35-8%; R
2O10-20%; Ni
2O3-7%; CdS2-4%; ZnO10-12%; Se1-3%; Fe
2O
30.5-1%.
Claims (1)
1, a kind of coloured glass brown colouring additive preparation technology is characterized in that adopting the preparation of following steps method:
(a) preparation of fusing assistant: the fusing assistant proportioning raw materials is: SiO
230-35%; Al
2O
36-10%; CaO0.5-2%; MgO0.2-1%; PbO45-50%; B
2O
34-8%; K
2O+Na
2O10-15%;
(b) preparation of melted glaze powder: fusing assistant is heated in crucible 1100-1200 ℃ by above-mentioned chemical constitution batching back and is founded, soak 40-60min, and through shrend, ball milling, drying, sieving obtains melted glaze powder;
(c) preparation of pigment, it is toner that bronzing agent adopts nickel, cadmium, iron, its composition of raw materials: Ni
2O20-30%; CdS8-12%; Fe
2O
31-2%; ZnO20-30%; Li
2CO
316-20%; Se2-4%; B
2O
36-10%, borax is earlier soluble in water, and powder adds behind all the other raw material blendings, mixes oven dry thoroughly, and ball milling sieves, and obtains pigment;
(d) preparation of tinting material: fusing assistant and pigment by fusion in crucible after 2: 1 mixed, are injected the cold water hardening crack then, and dry back fragmentation is sieved, the brown particle agent.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2004100235380A CN1318338C (en) | 2004-01-17 | 2004-01-17 | Colour glass brown colouring pigment and its preparing process |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB2004100235380A CN1318338C (en) | 2004-01-17 | 2004-01-17 | Colour glass brown colouring pigment and its preparing process |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1640834A CN1640834A (en) | 2005-07-20 |
CN1318338C true CN1318338C (en) | 2007-05-30 |
Family
ID=34868442
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB2004100235380A Expired - Fee Related CN1318338C (en) | 2004-01-17 | 2004-01-17 | Colour glass brown colouring pigment and its preparing process |
Country Status (1)
Country | Link |
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CN (1) | CN1318338C (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102190914A (en) * | 2011-03-09 | 2011-09-21 | 都匀开发区福田化工有限责任公司 | Formula of thermal-spraying colorants for toughened glass |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1055163A (en) * | 1990-03-27 | 1991-10-09 | 石家庄市第一玻璃厂 | Glass containing high lead low soda ash |
US5403664A (en) * | 1992-05-11 | 1995-04-04 | Nippon Electric Glass Co., Ltd. | Marble-like glass ceramic |
CN1204306A (en) * | 1995-12-21 | 1999-01-06 | 康宁股份有限公司 | Brown glass which absorbs ultraviolet radiation |
-
2004
- 2004-01-17 CN CNB2004100235380A patent/CN1318338C/en not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1055163A (en) * | 1990-03-27 | 1991-10-09 | 石家庄市第一玻璃厂 | Glass containing high lead low soda ash |
US5403664A (en) * | 1992-05-11 | 1995-04-04 | Nippon Electric Glass Co., Ltd. | Marble-like glass ceramic |
CN1204306A (en) * | 1995-12-21 | 1999-01-06 | 康宁股份有限公司 | Brown glass which absorbs ultraviolet radiation |
Non-Patent Citations (1)
Title |
---|
棕色啤酒瓶玻璃配方的设计 邵建亭等,西北轻工业学院学报,第14卷第1期 1996 * |
Also Published As
Publication number | Publication date |
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CN1640834A (en) | 2005-07-20 |
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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: 20070530 Termination date: 20110117 |