CN103102177B - Method for synthesizing zirconium silicate carbon-coated black pigment in situ - Google Patents

Method for synthesizing zirconium silicate carbon-coated black pigment in situ Download PDF

Info

Publication number
CN103102177B
CN103102177B CN201310072816.0A CN201310072816A CN103102177B CN 103102177 B CN103102177 B CN 103102177B CN 201310072816 A CN201310072816 A CN 201310072816A CN 103102177 B CN103102177 B CN 103102177B
Authority
CN
China
Prior art keywords
minutes
black pigment
temperature
heating
situ
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
CN201310072816.0A
Other languages
Chinese (zh)
Other versions
CN103102177A (en
Inventor
刘明泉
郑乃章
刘阳
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.)
Jingdezhen Ceramic Institute
Original Assignee
Jingdezhen Ceramic Institute
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 Jingdezhen Ceramic Institute filed Critical Jingdezhen Ceramic Institute
Priority to CN201310072816.0A priority Critical patent/CN103102177B/en
Publication of CN103102177A publication Critical patent/CN103102177A/en
Application granted granted Critical
Publication of CN103102177B publication Critical patent/CN103102177B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Pigments, Carbon Blacks, Or Wood Stains (AREA)
  • Glass Compositions (AREA)

Abstract

The invention discloses a method for synthesizing a zirconium silicate carbon-coated black pigment in situ. The black pigment with high coating rate is synthesized from powdery thermoset phenolic resin at the temperature of 1000-1100 DEG C by utilizing a nonhydrolytic sol-gel in-situ synthetic technology. The synthetic method disclosed by the invention has the advantages of simple process, high synthesis speed and low synthesis temperature; and the prepared black pigment is pure in color and stable in property, can be used at a temperature high up to 1300 DEG C, can be widely applied to the high-temperature glazes of various ceramic products and has high economic value.

Description

A kind of method of original position synthetic silicic acid zirconium parcel carbon black colorant
Technical field
The invention belongs to ceramic (pottery) field, be specifically related to a kind of method of original position synthetic silicic acid zirconium parcel carbon black colorant.
Background technology
In the black pigment using in Production of Ceramics at present, remove (Cr, Fe) 2o 3outside corundum type, other is spinel type colorant, as FeOFe 2o 3, Co-Cr-Fe, Co-Mn-Fe, Co-Mn-Cr-Fe, Co-Ni-Cr-Fe, Co-Mn-Ni-Cr-Fe, Co-Mn-Al-Cr-Fe, Co-Ni-Cr-Fe-Si etc.Although spinel type colorant Stability Analysis of Structures, have high temperature resistant, to atmosphere susceptibility little with the good feature of chemical stability, these colorants only in lime glaze colour generation best, and require in lime glaze without zinc, without magnesium, or low zinc, low magnesium.These colorants are unsettled in calcium magnesium glaze, are in most cases to form more stable spinel, make it to become grey or greyish-green; Although and stable in calcium zinc glaze, be off color, black middle band reddish-brown, and easily make glaze bubble.And black pigment FeOFe 2o 3easily be subject to the impact of atmosphere.Although manganese is conducive to black pigment colour generation, it tends to cause produce in glaze bubble.Cobalt is the distinct indispensable composition of black pigment, if but synthetic bad meeting is that colorant is general green or general red, and to prepare bright-coloured black pigment, the consumption of its cobalt oxide is more, and the price of cobalt oxide, a kind of black using in architectural pottery is produced oozes fancy glaze, and the composition of its colour generation is ruthenium salt, ruthenium is a kind of precious metal, and its price is tens times of gold., all there is certain deficiency in the existing technology of preparing of these black pigments in sum.Be subject to the impact of atmosphere (as FeOFe 2o 3) be subject to the impact of composition of glaze or price costliness very etc.
The stability of colorant is a difficult problem, especially high temperature (1300 ℃) colorant in Production of Ceramics always, only having at present cadmium-selenium red (Huang) colorant of zirconium silicate parcel is the colorant of high-temperature stable, and the Application and Development of the occlusion pigment of other colors there is not yet report.Therefore, developing the black occlusion pigment that can stablize color development under a kind of high temperature has great importance.
Summary of the invention
The technical problem to be solved in the present invention is to provide the method for the original position synthetic silicic acid zirconium parcel carbon black colorant that a kind of technique is simple, raw materials cost is lower, synthetic ratio is high, use temperature is high.
For solving above technical problem, technical scheme of the present invention is: a kind of method of original position synthetic silicic acid zirconium parcel carbon black colorant, in turn includes the following steps:
1. by the anhydrous ZrCl of technical pure 4join technical pure Si (OC 2h 5) 4in solution, control Zr + 4with Si + 4mol ratio is 1:1.2, and at room temperature high-speed stirring forms gel mixture A after 20 minutes;
2. powdered thermosetting resol, LiF are joined in dehydrated alcohol, the consumption of controlling powdered thermosetting resol is ZrCl 45 ~ 8% of weight, the concentration in dehydrated alcohol is 10%; Li + 1with Zr + 4mol ratio be 1:0.35, liquid B is uniformly mixed after stirring;
3. A mutually mixed and stirred with B, being then placed in 110 ℃ of oil bath pan reflux and obtaining precursor sol, then precursor sol being placed in to baking oven dry, obtaining xerogel;
4. xerogel is packed in crucible and adopt the method synthesizing black colorant of adding a cover conventional heating, synthesis technique control is: room temperature ~ 650 ℃, and the heating-up time is 5 minutes, is incubated 35 minutes; 650 ℃ ~ synthesis temperature, the heating-up time is 10 minutes, is incubated 10 minutes; Then naturally cooling.
Described synthesis temperature is 1000 ~ 1100 ℃.
Above-mentioned black pigment encapsulation ratio >=50%, mean particle size≤10 μ m, use temperature are 1300 ℃.
Innovation of the present invention is to adopt brand-new non-hydrolytic sol-gel in situ synthetic technology to synthesize the black pigment that encapsulation ratio is high at 1000 ~ 1100 ℃ of temperature, and this black pigment has been compared following characteristics with existing black pigment:
1, occlusion pigment colour generation is pure stable, can not be subject to the impact of the factors such as composition, firing atmosphere of glaze;
2, occlusion pigment use temperature reaches 1300 ℃;
3, the preparation technology of occlusion pigment is simple, resultant velocity is fast, encapsulation ratio is high, cost is low.
Embodiment
By embodiment, the present invention is further detailed explanation below.
Embodiment mono-:
The technical process that zirconium silicate parcel carbon black is prepared black pigment is:
The first step: by the anhydrous ZrCl of technical pure 4join technical pure Si (OC 2h 5) 4in solution, control Zr + 4with Si + 4mol ratio is 1:1.2, and at room temperature high-speed stirring forms gel mixture A after 20 minutes;
Second step: powdered thermosetting resol, LiF are joined in dehydrated alcohol, and the consumption of controlling powdered thermosetting resol is ZrCl 48% of weight, the concentration in dehydrated alcohol is 10%; Li + 1with Zr + 4mol ratio be 1:0.35, liquid B is uniformly mixed after stirring;
The 3rd step: A mutually mixed and stirred with B, be then placed in 110 ℃ of oil bath pan reflux and obtain precursor sol, then precursor sol being placed in to baking oven dry, obtaining xerogel;
The 4th step: xerogel is packed in crucible and adopts the method synthesizing black colorant of adding a cover conventional heating, and synthesis technique control is: room temperature ~ 650 ℃, the heating-up time is 5 minutes, is incubated 35 minutes; 650 ~ 1100 ℃, the heating-up time is 10 minutes, is incubated 10 minutes; Then naturally cooling, whole heat-processed does not need sealing and atmosphere protection.
Embodiment bis-:
The technical process that zirconium silicate parcel carbon black is prepared black pigment is:
The first step: by the anhydrous ZrCl of technical pure 4join technical pure Si (OC 2h 5) 4in solution, control Zr + 4with Si + 4mol ratio is 1:1.2, and at room temperature high-speed stirring forms gel mixture A after 20 minutes;
Second step: powdered thermosetting resol, LiF are joined in dehydrated alcohol, and the consumption of controlling powdered thermosetting resol is ZrCl 46% of weight, the concentration in dehydrated alcohol is 10%; Li + 1with Zr + 4mol ratio be 1:0.35, liquid B is uniformly mixed after stirring;
The 3rd step: A mutually mixed and stirred with B, be then placed in 110 ℃ of oil bath pan reflux and obtain precursor sol, then precursor sol being placed in to baking oven dry, obtaining xerogel;
The 4th step: xerogel is packed in crucible and adopts the method synthesizing black colorant of adding a cover conventional heating, and synthesis technique control is: room temperature ~ 650 ℃, the heating-up time is 5 minutes, is incubated 35 minutes; 650 ~ 1050 ℃, the heating-up time is 10 minutes, is incubated 10 minutes; Then naturally cooling, whole heat-processed does not need sealing and atmosphere protection.
Embodiment tri-:
The technical process that zirconium silicate parcel carbon black is prepared black pigment is:
The first step: by the anhydrous ZrCl of technical pure 4join technical pure Si (OC 2h 5) 4in solution, control Zr + 4with Si + 4mol ratio is 1:1.2, and at room temperature high-speed stirring forms gel mixture A after 20 minutes;
Second step: powdered thermosetting resol, LiF are joined in dehydrated alcohol, and the consumption of controlling powdered thermosetting resol is ZrCl 45% of weight, the concentration in dehydrated alcohol is 10%; Li + 1with Zr + 4mol ratio be 1:0.35, liquid B is uniformly mixed after stirring;
The 3rd step: A mutually mixed and stirred with B, be then placed in 110 ℃ of oil bath pan reflux and obtain precursor sol, then precursor sol being placed in to baking oven dry, obtaining xerogel;
The 4th step: xerogel is packed in crucible and adopts the method synthesizing black colorant of adding a cover conventional heating, and synthesis technique control is: room temperature ~ 650 ℃, the heating-up time is 5 minutes, is incubated 35 minutes; 650 ~ 1000 ℃, the heating-up time is 10 minutes, is incubated 10 minutes; Then naturally cooling, whole heat-processed does not need sealing and atmosphere protection.
It is as follows that the encapsulation ratio of the obtained black pigment of above-described embodiment 1-3 and average granularity carry out characterization result:
Figure 563015DEST_PATH_IMAGE001
Listed is above only zirconium silicate parcel black pigment preparation method's of the present invention preferred embodiment, certainly can not limit with this interest field of the present invention, therefore the equivalent variations of doing according to the present patent application the scope of the claims, still belongs to the scope that the present invention is contained.

Claims (1)

1. original position synthetic silicic acid zirconium wraps up a method for carbon black colorant, in turn includes the following steps:
1. by the anhydrous ZrCl of technical pure 4join technical pure Si (OC 2h 5) 4in solution, control Zr + 4with Si + 4mol ratio is 1:1.2, and at room temperature high-speed stirring forms gel mixture A after 20 minutes;
2. powdered thermosetting resol, LiF are joined in dehydrated alcohol, the consumption of controlling powdered thermosetting resol is ZrCl 45 ~ 8% of weight, the concentration in dehydrated alcohol is 10%; Li + 1with Zr + 4mol ratio be 1:0.35, liquid B is uniformly mixed after stirring;
3. A mutually mixed and stirred with B, being then placed in 110 ℃ of oil bath pan reflux and obtaining precursor sol, then precursor sol being placed in to baking oven dry, obtaining xerogel;
4. xerogel is packed in crucible and adopt the method synthesizing black colorant of adding a cover conventional heating, synthesis technique control is: room temperature ~ 650 ℃, and the heating-up time is 5 minutes, is incubated 35 minutes; 650 ℃ ~ synthesis temperature, the heating-up time is 10 minutes, is incubated 10 minutes; Then naturally cooling;
Described synthesis temperature is 1000 ~ 1100 ℃;
Described black pigment encapsulation ratio >=50%, mean particle size≤10 μ m, use temperature are 1300 ℃.
CN201310072816.0A 2013-03-07 2013-03-07 Method for synthesizing zirconium silicate carbon-coated black pigment in situ Expired - Fee Related CN103102177B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201310072816.0A CN103102177B (en) 2013-03-07 2013-03-07 Method for synthesizing zirconium silicate carbon-coated black pigment in situ

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201310072816.0A CN103102177B (en) 2013-03-07 2013-03-07 Method for synthesizing zirconium silicate carbon-coated black pigment in situ

Publications (2)

Publication Number Publication Date
CN103102177A CN103102177A (en) 2013-05-15
CN103102177B true CN103102177B (en) 2014-03-26

Family

ID=48310416

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201310072816.0A Expired - Fee Related CN103102177B (en) 2013-03-07 2013-03-07 Method for synthesizing zirconium silicate carbon-coated black pigment in situ

Country Status (1)

Country Link
CN (1) CN103102177B (en)

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101182236A (en) * 2007-11-15 2008-05-21 广东东鹏陶瓷股份有限公司 Zirconium silicate coated ceramic pigment and method for making same
CN101870475B (en) * 2010-06-09 2012-02-01 景德镇陶瓷学院 Method for low-temperature synthesis of zirconium silicate powder through non-hydrolytic sol-gel reaction by using zirconium acetate as zirconium source
CN102433033B (en) * 2011-09-02 2014-03-05 景德镇陶瓷学院 Method for preparing carbon black inclusion pigment in situ by nonhydrolytic sol-gel process

Also Published As

Publication number Publication date
CN103102177A (en) 2013-05-15

Similar Documents

Publication Publication Date Title
CN103113137B (en) Method for preparing black pigment by wrapping carbon black with zirconium silicate
CN102432340B (en) Method for preparing zirconium silicate-based ceramic pigment by nonhydrolytic sol-gel process
CN101844920A (en) Preparation method of colored zirconia ceramics
CN103086749B (en) In-situ synthesis method of zirconium silicate encapsulated carbon black pigment by microwave heating
CN101973788A (en) Preparation method of phase-separation peacock blue glaze
CN103274765A (en) Co-Zn-Cr-Al composite spinel type blue ceramic pigment and preparation method thereof
CN102817072A (en) Preparation method of doping raw material used for growing gem single crystal through edge-defined film-fed growth method
CN108975869A (en) A kind of heat-insulated sensitization discoloration glaze ceramic and preparation process
CN106045555B (en) Ceramic pug and preparation method thereof
CN109266040B (en) High-temperature red ceramic pigment and preparation method thereof
CN103113136B (en) Preparation method of zirconium silicate wrapped carbon black pigment by microwave synthesis
JP3728505B2 (en) Method for producing Al-substituted hematite
CN105254337B (en) It is a kind of that the method that high colour developing zirconium silicate wraps up carbon black colorant is prepared by carbon source of string
CN107777727B (en) A kind of preparation method of Ba-Al-Mn-O blue inorganic pigment
CN110981472B (en) High-strength green zirconia ceramic powder and preparation method and application thereof
CN103102177B (en) Method for synthesizing zirconium silicate carbon-coated black pigment in situ
CN105524491B (en) A kind of preparation method of iron oxide red composite pigment
CN105036148B (en) Preparation method for flowerlike Li2Si2O5 powder
CN105000911A (en) Preparation method of purple ceramic pigment with cobalt-silicon olivine structure
CN101445397B (en) Two-step method for preparing high-temperature red ceramic color with nuclear shell structure
CN101608072A (en) A kind of red pigment and preparation method thereof
CN101973789B (en) Preparation method of split-phase blue lily glaze
CN110684371B (en) Cr-doped Bi24Al2O39Metal oxide mixed phase red inorganic pigment and preparation method thereof
CN101439986B (en) Method for preparing core-shell structured high temperature red ceramic pigment by in-situ synthesis
CN106276990A (en) Heavy anhydrous magnesium carbonate, the preparation method of magnesium oxide

Legal Events

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

Granted publication date: 20140326

Termination date: 20160307

CF01 Termination of patent right due to non-payment of annual fee