CN102173867A - Method for preparing zirconium iron pink pigment from electrically-melted zirconium oxide - Google Patents

Method for preparing zirconium iron pink pigment from electrically-melted zirconium oxide Download PDF

Info

Publication number
CN102173867A
CN102173867A CN2011100310907A CN201110031090A CN102173867A CN 102173867 A CN102173867 A CN 102173867A CN 2011100310907 A CN2011100310907 A CN 2011100310907A CN 201110031090 A CN201110031090 A CN 201110031090A CN 102173867 A CN102173867 A CN 102173867A
Authority
CN
China
Prior art keywords
zirconium
electric
melting zirconia
iron pink
electrically
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
CN2011100310907A
Other languages
Chinese (zh)
Other versions
CN102173867B (en
Inventor
程诗忠
刘少名
叶旦旺
陈康宁
朱忠雄
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.)
FUJIAN SANXIANG ADVANCED MATERIALS Co Ltd
Original Assignee
FUJIAN SANXIANG ADVANCED MATERIALS Co 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 FUJIAN SANXIANG ADVANCED MATERIALS Co Ltd filed Critical FUJIAN SANXIANG ADVANCED MATERIALS Co Ltd
Priority to CN 201110031090 priority Critical patent/CN102173867B/en
Publication of CN102173867A publication Critical patent/CN102173867A/en
Application granted granted Critical
Publication of CN102173867B publication Critical patent/CN102173867B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Inorganic Compounds Of Heavy Metals (AREA)
  • Compounds Of Iron (AREA)

Abstract

The invention discloses a method for preparing zirconium iron pink pigment from electrically-melted zirconium oxide. The method comprises the following steps of: 1) reshaping crystal appearance, namely performing zirconium oxide crystal appearance spheroidization on the common electrically-melted zirconium oxide powder by using a special device, so that the appearance of the electrically-melted zirconium oxide tends to be close to a spherical state; 2) removing impurities, namely washing the product obtained in the step 1) with diluted acid until the content of the impurities such as aluminium oxide (Al2O3), ferric oxide (Fe2O3), silicon oxide (SiO2), phosphorus pentoxide (P2O5) and the like is less than 0.1 percent, and then drying; 3) controlling granularity, namely grinding the electrically-melted zirconium oxide with impurities removed and controlling the granularity of the electrically-melted zirconium oxide to be 0 to 5 mu m; and 4) preparing samples, namely weighing the electrically-melted zirconium oxide obtained in the step 3), zirconium iron pink and other raw materials, mixing the materials completely and uniformly, grinding the mixture finely, heating the mixture to calcine for 5 hours, preserving heat for 1 hour when the temperature is 1,000 to 1,100 DEG C, cooling, and taking out the product. By the method, influence of reaction impurities is removed; reaction activity is improved; and the zirconium iron pink pigment is prepared from the electrically-melted zirconium oxide instead of zirconium, so the production cost of the zirconium iron pink pigment is reduced.

Description

Electric-melting zirconia is produced the method for zirconium-iron pink pigment
Technical field
The present invention relates to a kind of electric-melting zirconia and produce the method for zirconium-iron pink pigment.
Background technology
At present the ceramic pigment industry is seldom produced zirconium-iron pink pigment with electric-melting zirconia, mainly be the composition principle of zirconium-iron pink pigment to be different from other zirconiums be colorant such as praseodymium yellow and vanadium orchid etc., zirconium-iron pink pigment belongs to half coated colorant.And electric-melting zirconia composition and active aspect do not reach chemical zirconium requirement, aluminum oxide and titanium oxide impurity are little in content height, the reactive behavior of electric-melting zirconia, therefore can not produce zirconium-iron pink pigment by the instead of chemical zirconium, but chemical zirconium production cost height causes the production cost of zirconium-iron pink pigment higher.
Summary of the invention
The technical problem to be solved in the present invention provides the method that low, the active high electric-melting zirconia of a kind of foreign matter content is produced zirconium-iron pink pigment.
In order to solve the problems of the technologies described above, the technical solution adopted for the present invention to solve the technical problems is: provide a kind of electric-melting zirconia to produce the method for zirconium-iron pink pigment, may further comprise the steps:
1): brilliant looks change shape and handle: with common electric-melting zirconia powder, carry out the spheroidizing of zirconium white powder crystal looks by special device, make the pattern of electric-melting zirconia be tending towards the subglobular state;
2) remove impurity: the step 1) products therefrom is washed to impurity A l with diluted acid 2O 3, Fe 2O 3, SiO 2, P 2O 5Content is washed the back oven dry respectively less than 0.1% (quality);
3) granularity control: to step 2) electric-melting zirconia of removing behind the impurity grinds, and the granularity of electric-melting zirconia is controlled between 0~5 μ m;
4) preparation sample: the electric-melting zirconia of weighing step 3) gained and other raw materials of zirconium iron pink, fully evenly mixed and levigate after, heating and calcining 5 hours, insulation is 1 hour when reaching 1000-1100 ℃, cooling cooling back taking-up.
Wherein, to step 2) electric-melting zirconia after the pickling carries out spectral measurement, foreign matter content continued electric-melting zirconia is carried out pickling greater than 0.1% o'clock, until foreign matter content each less than 0.06% (quality).
Wherein, described diluted acid is 1% (quality) dilute sulphuric acid or dilute hydrochloric acid.
Wherein, the control of step 3) granularity is ground by ball-grinding machine, and observes control by laser particle analyzer.
Wherein, the described holding temperature of step 4) is 1050 ℃.
The invention has the beneficial effects as follows that by removing the electric-melting zirconia that the control of impurity and granularity is produced, removed the reaction impurities influence, it is big to improve reactive behavior, can produce zirconium-iron pink pigment by the instead of chemical zirconium, reduced the production cost of zirconium-iron pink pigment.
Description of drawings
Below in conjunction with accompanying drawing the specific embodiment of the present invention is described in further detail.
Fig. 1 is the process flow sheet that electric-melting zirconia of the present invention is produced zirconium-iron pink pigment.
Embodiment
By describing technology contents of the present invention, structural attitude in detail, realized purpose and effect, give explanation below in conjunction with embodiment and conjunction with figs. are detailed.
Referring to technical process Fig. 1, electric-melting zirconia of the present invention is produced the method for zirconium-iron pink pigment, may further comprise the steps:
1): brilliant looks change shape and handle: with common electric-melting zirconia powder, carry out the spheroidizing of zirconium white powder crystal looks by special device, make the pattern of electric-melting zirconia be tending towards the subglobular state;
2) remove impurity: the step 1) products therefrom is washed with diluted acid, and described diluted acid can be 1% (quality) dilute sulphuric acid or dilute hydrochloric acid, pickling impurity A l to the electric-melting zirconia 2O 3, Fe 2O 3, SiO 2, P 2O 5Content is got sample segment by spectral detection such as ray fluorescence spectrometer, if Al respectively less than 0.1% (quality) in the process 2O 3, Fe 2O 3, SiO 2, P 2O 5Content continues electric-melting zirconia is carried out pickling, until Al during greater than 0.1% (quality) 2O 3, Fe 2O 3, SiO 2, P 2O 5Content less than 0.1% (quality) after, with the oven dry of the electric-melting zirconia of removal of impurities;
3) granularity control: to step 2) electric-melting zirconia behind the removal impurity grinds, and process adopts post-type mixer to grind, and observes by the Ma Erwen particle size analyzer, and the granularity of control electric-melting zirconia is between 0~5 μ m;
4) preparation sample: the electric-melting zirconia of weighing step 3) gained and other raw materials of zirconium iron pink, according to the prescription thorough mixing, use the dry bulb mill to carry out mixed grinding in the process, levigate back heating and calcining 5 hours in cabinet-type electric furnace or High Temperature Furnaces Heating Apparatus, temperature is set to 1000-1100 ℃, be incubated 1 hour after reaching preset temp, take out the cooling back.
The zirconium-iron pink pigment of treated electric-melting zirconia preparation is tested by color development, and is as shown in table 1, and the color development experimental result shows with respect to the effect that is significantly improved before handling, the zirconium-iron pink pigment of the nearly chemical zirconium preparation of its illuminant colour differential.
Figure BDA0000045805510000031
Table 1
Effectively reduce Al in the electric-melting zirconia by above-mentioned steps 2O 3, Fe 2O 3, SiO 2, P 2O 5Content, reduce the influence of reaction impurities, and the granularity of control electric-melting zirconia, improve its reactive behavior, more help the production of zirconium-iron pink pigment, substituted chemistry zirconium fully, the production cost of reduction zirconium-iron pink pigment.
In the present embodiment, step 2) remove the process of impurity, generally can be with Al 2O 3, Fe 2O 3, SiO 2, P 2O 5Content to reduce to respectively be 0.06% (quality), can ignore the influence of impurity this moment in electric-melting zirconia prepares the production of zirconium-iron pink pigment, reach the ideal effect.
In the present embodiment, the described best holding temperature of step 4) is 1050 ℃, and insulation is 1 hour under this temperature, makes that the preparation process material reaction is complete.
The above only is embodiments of the invention; be not so limit claim of the present invention; every equivalent structure or equivalent flow process conversion that utilizes specification sheets of the present invention and accompanying drawing content to be done; or directly or indirectly be used in other relevant technical fields, all in like manner be included in the scope of patent protection of the present invention.

Claims (6)

1. the method that electric-melting zirconia is produced zirconium-iron pink pigment is characterized in that, may further comprise the steps:
1) brilliant looks change the shape processing: with the electric-melting zirconia powder, carry out the spheroidizing of zirconium white powder crystal looks by grinding, make the pattern of electric-melting zirconia be tending towards the subglobular state;
2) remove impurity: the step 1) products therefrom is washed to impurity A l with diluted acid 2O 3, Fe 2O 3, SiO 2, P 2O 5Deng content each less than 0.1% (quality), wash back oven dry;
3) granularity control: to step 2) electric-melting zirconia of removing behind the impurity grinds, and the granularity of electric-melting zirconia is controlled between 0~5 μ m;
4) preparation sample: the electric-melting zirconia of weighing step 3) gained and other raw materials of zirconium iron pink, fully evenly mixed and levigate after, heating and calcining 5 hours, insulation is 1 hour when reaching 1000-1100 ℃, cooling cooling back taking-up.
2. electric-melting zirconia according to claim 1 is produced the method for zirconium-iron pink pigment, it is characterized in that step 2) in, electric-melting zirconia after the pickling carries out spectral measurement, foreign matter content is greater than 0.1% o'clock, continue electric-melting zirconia is carried out pickling, until foreign matter content less than 0.1%.
3. electric-melting zirconia according to claim 2 is produced the method for zirconium-iron pink pigment, it is characterized in that step 2) removal impurity A l 2O 3, Fe 2O 3, SiO 2, P 2O 5Until content each less than 0.06% (quality).
4. according to any method that described electric-melting zirconia is produced zirconium-iron pink pigment of claim 1 to 3, it is characterized in that described diluted acid is the dilute sulphuric acid or the dilute hydrochloric acid of 1% (quality).
5. electric-melting zirconia according to claim 1 is produced the method for zirconium-iron pink pigment, it is characterized in that, the control of step 3) granularity is ground by ball-grinding machine, and observes control by laser particle analyzer.
6. electric-melting zirconia according to claim 1 is produced the method for zirconium-iron pink pigment, it is characterized in that the described holding temperature of step 4) is 1050 ℃.
CN 201110031090 2011-01-28 2011-01-28 Method for preparing zirconium iron pink pigment from electrically-melted zirconium oxide Active CN102173867B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 201110031090 CN102173867B (en) 2011-01-28 2011-01-28 Method for preparing zirconium iron pink pigment from electrically-melted zirconium oxide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 201110031090 CN102173867B (en) 2011-01-28 2011-01-28 Method for preparing zirconium iron pink pigment from electrically-melted zirconium oxide

Publications (2)

Publication Number Publication Date
CN102173867A true CN102173867A (en) 2011-09-07
CN102173867B CN102173867B (en) 2013-04-24

Family

ID=44517165

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 201110031090 Active CN102173867B (en) 2011-01-28 2011-01-28 Method for preparing zirconium iron pink pigment from electrically-melted zirconium oxide

Country Status (1)

Country Link
CN (1) CN102173867B (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103466697A (en) * 2013-09-10 2013-12-25 圣泉(福建)制釉有限公司 Preparation method and application of active zirconium dioxide
CN104529541A (en) * 2014-12-05 2015-04-22 三祥新材股份有限公司 Preparation method for modified fused zirconia and praseodymium yellow pigment
CN105733310A (en) * 2016-01-26 2016-07-06 三祥新材股份有限公司 Pretreatment method of zircon powder and preparation method of vanadium-zirconium blue material
CN105753510A (en) * 2014-12-05 2016-07-13 三祥新材股份有限公司 Preparation method of high-temperature-resistant modified fused zirconia and praseodymium yellow pigment
CN108384278A (en) * 2018-03-06 2018-08-10 三祥新材股份有限公司 A kind of production method of ink-jet pr-yellow material electric-melting zirconia
CN113264673A (en) * 2021-06-08 2021-08-17 三祥新材股份有限公司 Method for producing yellowish-red zirconium-iron-red regulating pigment by electrically melting zirconia

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101381245A (en) * 2008-10-20 2009-03-11 福建三祥工业新材料有限公司 Method for improving electrofusion zirconia chromophoric redness value

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101381245A (en) * 2008-10-20 2009-03-11 福建三祥工业新材料有限公司 Method for improving electrofusion zirconia chromophoric redness value

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
刘福田等: "锆英石基陶瓷颜料的合成机理", 《山东建材学院学报》, vol. 12, no. 01, 31 March 1998 (1998-03-31) *
吴建锋等: "锆铁红色料的研究", 《佛山陶瓷》, no. 04, 31 December 1999 (1999-12-31) *
闫浩等: "锆系颜料的制备", 《中国陶瓷》, no. 01, 31 December 1991 (1991-12-31) *

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103466697A (en) * 2013-09-10 2013-12-25 圣泉(福建)制釉有限公司 Preparation method and application of active zirconium dioxide
CN105859325B (en) * 2014-12-05 2018-09-25 三祥新材股份有限公司 A kind of preparation method of pr-yellow material
CN104529541A (en) * 2014-12-05 2015-04-22 三祥新材股份有限公司 Preparation method for modified fused zirconia and praseodymium yellow pigment
CN105753510A (en) * 2014-12-05 2016-07-13 三祥新材股份有限公司 Preparation method of high-temperature-resistant modified fused zirconia and praseodymium yellow pigment
CN105859325A (en) * 2014-12-05 2016-08-17 三祥新材股份有限公司 Preparation method for praseodymium yellow pigment
CN105753510B (en) * 2014-12-05 2018-05-01 三祥新材股份有限公司 A kind of preparation method of heat resist modification electric-melting zirconia and pr-yellow material
CN108624087A (en) * 2016-01-26 2018-10-09 三祥新材股份有限公司 A kind of preprocess method for the zirconium English powder that reactivity is high
CN108610658A (en) * 2016-01-26 2018-10-02 三祥新材股份有限公司 A kind of preparation method of zircon-vanadium blue pigment at low cost
CN105733310A (en) * 2016-01-26 2016-07-06 三祥新材股份有限公司 Pretreatment method of zircon powder and preparation method of vanadium-zirconium blue material
CN108610658B (en) * 2016-01-26 2020-10-27 三祥新材股份有限公司 Preparation method of low-cost vanadium-zirconium blue pigment
CN108624087B (en) * 2016-01-26 2020-10-27 三祥新材股份有限公司 Pretreatment method of zircon powder with high reaction activity
CN108384278A (en) * 2018-03-06 2018-08-10 三祥新材股份有限公司 A kind of production method of ink-jet pr-yellow material electric-melting zirconia
CN113264673A (en) * 2021-06-08 2021-08-17 三祥新材股份有限公司 Method for producing yellowish-red zirconium-iron-red regulating pigment by electrically melting zirconia

Also Published As

Publication number Publication date
CN102173867B (en) 2013-04-24

Similar Documents

Publication Publication Date Title
CN102173867B (en) Method for preparing zirconium iron pink pigment from electrically-melted zirconium oxide
CN106082671B (en) Longquan celadon blueness glaze, Longquan celadon and preparation method thereof
CN102923752A (en) New method for decolorizing and whitening phosphogypsum
CN105733310B (en) The preprocess method of zirconium English powder and the preparation method of zircon-vanadium blue pigment
CN109054452A (en) Copper-chromium black pigment and preparation method thereof
CN109721357A (en) A kind of Zirconium oxide powder and its preparation method and application that the nanometer yttrium that monodisperse granularity is controllable is stable
CN103145453A (en) Praseodymium yellow material for ceramic ink and preparation method thereof
CN108516578A (en) A kind of sub-micron indium oxide raw powder's production technology
CN109850941B (en) Method for preparing high-purity titanium dioxide by hydrolyzing industrial titanium sulfate solution
CN102659392A (en) Preparation method of calcined alumina powder for black ceramics
CN109370258A (en) The production method of the good zircon-vanadium blue pigment of hair color effect
CN108069431A (en) A kind of synthetic method of high-purity amorphous boron powder
CN104892030B (en) A kind of preparation method of nanometer praseodymium yellow ceramic pigment
CN110951281B (en) Copper-chromium black toner prepared by solid-phase sintering method promoted by molybdenum oxide and zinc oxide and preparation method thereof
CN108950181A (en) A kind of preparation process of beryllium oxide
CN102775191B (en) Seed crystal introduced chromium tin pink ceramic pigment and preparation method thereof
CN104058764A (en) Preparation method for infrared energy-saving paint
CN102583515A (en) Method for preparing CaTiO3 composite material from slow-cooling titanium-bearing blast furnace slag
CN105860596B (en) A kind of method for improving electric-melting zirconia specific surface area and reactivity
CN103396685A (en) Preparation method of energy-saving paint
CN104891857A (en) Preparation method of stabilizer composite zirconium oxide powder
CN108455665A (en) The method that successive reaction prepares rutile type nano titanic oxide
CN114671460A (en) Method for removing impurities from industrial metatitanic acid in sulfuric acid method titanium dioxide short-flow process
CN108585040B (en) CeVO4Quick preparation method of functional material
CN107311223B (en) A kind of sheet magnesium titanate potassium and preparation method thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C53 Correction of patent of invention or patent application
CB02 Change of applicant information

Address after: 355500 Fujian city of Ningde province Shouning County Chengguan liberation Street No. 292

Applicant after: Sanxiang Advanced Materials Co., Ltd.

Address before: 355500 Fujian city of Ningde province Shouning County Chengguan liberation Street No. 292

Applicant before: Fujian Sanxiang Advanced Materials Co., Ltd.

COR Change of bibliographic data

Free format text: CORRECT: APPLICANT; FROM: FUJIAN SANXIANG ADVANCED INDUSTRIAL MATERIALS CO., LTD. TO: SANXIANG ADVANCED MATERIALS CO., LTD.

C14 Grant of patent or utility model
GR01 Patent grant