CN1163416C - Method for producing cobalt oxide nickel oxide powder for electronic industry - Google Patents
Method for producing cobalt oxide nickel oxide powder for electronic industry Download PDFInfo
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- CN1163416C CN1163416C CNB941118207A CN94111820A CN1163416C CN 1163416 C CN1163416 C CN 1163416C CN B941118207 A CNB941118207 A CN B941118207A CN 94111820 A CN94111820 A CN 94111820A CN 1163416 C CN1163416 C CN 1163416C
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- cobalt
- oxalate
- nickel
- oxide powder
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Abstract
The present invention relates to a method for producing cobalt oxide powder and nickel oxide powder used for electronic industry, the technological steps of which comprise: preparation of a cobalt nitrate solution and a nickel nitrate solution; ammonium oxalate preparation; cobalt oxalate and nickel oxalate preparation by a settlement reaction; filtration and washing; cobalt oxide powder and nickel oxide powder preparation by roasting cobalt oxalate and nickel oxalate. The method has the advantage of simple technology; furthermore, the method can be used for producing the high-purity cobalt oxide powder and the high-purity nickel oxide powder of which the Fisher diameter size is less than 1 micrometer and the grain fineness is less than 500 A, and an electronic element has the advantages of good stability, good reliability and great enhancement of electrical properties by using the powder as a doping material.
Description
The invention belongs to the production method of used in electronic industry cobalt oxide, nickel oxide powder, they are used to do the dopant material of electronic components such as thermistor, voltage dependent resistor, picture tube glass bulb.
In China's Chemicals, the preparation method of cobalt oxide, nickel oxide powder generally is to be raw material with the carbonate of cobalt or nickel, nitrate or oxyhydroxide, gets through calcining, and also having with cobalt chloride (nickel) is raw material, add ammonium oxalate and generate cobalt oxalate (nickel) precipitation, calcining and getting in air again.The product that aforesaid method obtains, basic metal and alkaline earth metal content are higher, and coarse size does not have the physics specification requirement again, does not therefore meet the requirement of electronic component adulterated powder material.
Japanese Patent JP2208227A discloses a kind of method for preparing the low density cobalt oxide, and this method is that the reaction of raw material and oxalic acid or ammonium oxalate generates cobalt oxalate with the cobalt chloride solution; Or be that raw material and heavy carbonic alkali reaction generate cobalt carbonate hydroxide with the cobalt nitrate solution, and then add oxalic acid and generate cobalt oxalate; Filtration, washing, drying are after roasting cobalt oxalate and make cobalt oxide powder must pass to oxygen during roasting.Produce electronic component adulterated powder material with this kind method and have following problem: 1. be raw material with the cobalt chloride, influence the Cl of electrical property
-The ion-cleaning difficulty also is difficult for removing in follow-up calcining process; 2. be raw material with the Xiao Suangu,, operation increased, and make the easy Na of introducing in the product owing to exist Xiao Suangu to be converted into the middle operation of cobalt carbonate hydroxide
+, K
+The ion of doping element electrical property Deng having a strong impact on; 3. dry, roasting is carried out respectively, must lead to oxygen during roasting, has both increased equipment, makes complicated operationization again.
The objective of the invention is to overcome the deficiency that oneself has technology, the production method of a kind of used in electronic industry cobalt oxide, nickel oxide powder is provided, this kind method not only technology is simple, and prepared product is the high-quality dopant material of electronic component.
The object of the present invention is achieved like this: purity requirement and physical index according to the electronic component dopant material are improved existing technology, processing parameter to starting material and precipitin reaction is optimized selection and combination emphatically, and simplifies working process as far as possible, reduces cost.Method provided by the present invention, its processing step and corresponding technological conditions are as follows:
1. cobalt salt, nickel salt solution preparation
Cobalt salt, nickel salt solution are Xiao Suangu, nickel nitrate solution, and highly purified electrolytic metal cobalt, metallic nickel are made with nitric acid dissolve, and the cobalt contents in the solution, nickel content are controlled at 100～300 grams per liters, and free acid is controlled at below 10 grams per liters.
2. ammonium oxalate preparation
With 90～100 ℃ of deionized water dissolvings, specific gravity control adds industrial ammonia then 1.03～1.05 with oxalic acid, and the pH value is controlled at 2.0～5.0, temperature be controlled at 40～80 ℃ stand-by.
3. cobalt oxalate, nickelous oxalate are produced in precipitin reaction
Entire reaction is under agitation carried out, stirring velocity is 60～80 rev/mins, the temperature of Xiao Suangu, nickel nitrate solution is 30～50 ℃, ammonium oxalate joins in Xiao Suangu, the nickel nitrate solution with 20～50 liters/minute flow velocity, its add-on is determined by endpoint pH, endpoint pH is 0.5～2.5, and the reaction times is 15～30 minutes.
4. filter, wash
Sedimentary cobalt oxalate, nickelous oxalate are filtered and wash with hot water (deionized water), and the pH value of last elutant is controlled at 5.0～7.0.
5. roasting cobalt oxalate, nickelous oxalate are produced cobalt oxide, nickel oxide powder
Need not be dry before the roasting, directly will wash cobalt oxalate, the nickelous oxalate of getting well and put into special stoving oven and carry out roasting, need not lead to oxygen during roasting, maturing temperature is 300～500 ℃, roasting time is 4～5 hours.
The present invention has the following advantages:
According to method provided by the present invention can prepare high purity, (Fisher particle size is less than 1 μ m to have specific physical specification, grain fineness number is less than 500 ) cobalt oxide, nickel oxide powder, can satisfy the requirement of the required corresponding dopant materials of electronic devices and components such as piezoresistor, thermistor.
2. cobalt oxide, the nickel oxide powder that adopts the present invention to produce made the electronic devices and components that dopant material is produced, and makes the electronic devices and components of dopant material production with chemical reagent of the same name and compares, and its electrical property improves a lot, stability and good reliability.
3. adopt the flouring technology of nitrate process simple, and avoided influencing the chlorion of doping element electrical property than villaumite legal system powder craft washing process.
4. Xiao Suangu, nickelous nitrate are directly made cobalt oxalate, nickelous oxalate with the ammonium oxalate reaction, and cancel drying process, simplified technology, reduced energy consumption, reduced working strength of workers.
Embodiment 1:
It is to dissolve in 30% the industrial nitric acid that the gradation of electrolytic metal cobalt is added concentration, and cobalt contents is controlled at 160 grams per liters, and free acid is controlled at 10 grams per liters, and the content of impurity such as Fe, Ca, Mg, Pb is less than 100ppm; With the boiling deionized water oxalic acid is dissolved, specific gravity control adds industrial ammonia 1.04, and the pH value is controlled at 4.5, and temperature is controlled at 70 ℃; Get 200 liters of cobalt nitrate solutions in reactor, be warming up to 45 ℃, then under agitation (60 rev/mins of stirring velocitys) adds ammonium oxalate in the reactor with 40 liters/minute flow velocitys, and endpoint pH is controlled at about about 1.0, reinforced finishing still continues to stir, and transformation time is 20 minutes; Cobalt oxalate precipitation filtered and with deionized water wash eight times, the pH value of elutant is 6.5 for the last time; The cobalt oxalate that washing is good was put into stoving oven, 400 ℃ of roastings 5 hours; Obtain the 42kg cobalt oxide after sieving, its technical indicator is as follows:
Co content 72.3%
Foreign matter content Cu300 Si200 Fe100 K50
(ppm) Al300 Ni1000 Ca200 Na150
Fisher particle size 0.8 μ m
Thing phase α-Co
3O
4
Grain fineness number 450
The cobalt oxide powder of present embodiment preparation is applicable to the dopant material of making piezoresistor.
Embodiment 2:
With highly purified electrolytic metal cobalt concentration is the dissolving of 30% industrial nitric acid, and cobalt contents is 170 grams per liters in the solution, free acid 10 grams per liters, and foreign matter content is less than 100ppm; The ammonium oxalate pH value of being prepared is 4.0, and temperature is 60 ℃; Cobalt nitrate solution is heated to 40 ℃, and under agitation (80 rev/mins) add the flow velocity of ammonium oxalate with 30 liters/minute in the reactor of containing Xiao Suangu, and endpoint pH is about about 1.0, and reinforced finishing still continues to stir, and the reaction times is 25 minutes; Cobalt oxalate precipitation filtered and with 80 ℃ deionized water wash 6 times; The cobalt oxalate that washing is good was put into stoving oven, 400 ℃ of roastings 4 hours; The technical indicator of gained cobalt oxide powder is as follows after sieving:
Co content 71.8%
Foreign matter content Na50 Ca70 SO
45 Fe80
(ppm) Ni300 Mg100 Cu100 Al150
Fisher particle size 0.5 μ m
Thing phase α-Co
3O
4
Grain fineness number 250
Cobalt oxide powder in the present embodiment is applicable to the dopant material of making thermistor.
Implement 3:
With highly purified electrolytic metal nickel concentration is the dissolving of 40% industrial nitric acid, and Ni content is 140 grams per liters in the solution, and free acid is 10 grams per liters, and foreign matter content is less than 100ppm; With boiling deionized water dissolving oxalic acid, proportion is 1.03, adds industrial ammonia, and the pH value is controlled at 3.0, and temperature is controlled at 70 ℃; Get 200 liters of nickel nitrate solutions in reactor, be warming up to 35 ℃, under agitation (rotating speed is 60 rev/mins) adds ammonium oxalate in the reactor with 40 liters/minute flow velocitys, and it is about about 2.0 that the pH value is controlled at, and reinforced finishing still continues to stir, and the reaction times is 20 minutes; Nickelous oxalate is filtered the back with＞70 ℃ deionized water wash eight times; The nickelous oxalate that washing is good was put into stoving oven, 400 ℃ of roastings 4 hours; Obtain the 36kg nickel oxide powder after sieving, its technical indicator is as follows:
Ni content 73.4%
Foreign matter content Cu30 Si20 Cl10 Ca300
(ppm) Co150 NO
3100 Fe100 Mg300
SO
420 Na50 Al100
Fisher particle size 0.5 μ m
Thing phase α-NiO is a main body
Grain fineness number 300
Nickel oxide powder in the present embodiment is applicable to the dopant material of making thermistor.
Embodiment 4:
With highly purified electrolytic nickel concentration is the dissolving of 40% industrial nitric acid, and nickel content is 180 grams per liters, and free acid is 8 grams per liters; Foreign matter content is less than 100ppm; The pH value of ammonium oxalate is 2.5, and temperature is 60 ℃; Nickel nitrate solution is heated to 50 ℃, and under agitation (60 rev/mins) add ammonium oxalate with 25 liters/minute flow velocity, and it is about about 2.0 that endpoint pH is controlled at, and reinforced finishing continues to stir, and the reaction times is 20 minutes; Nickelous oxalate filtered and with 80 ℃ deionized water wash eight times; The nickelous oxalate that washing is good was put into stoving oven, 400 ℃ of roastings 5 hours; The technical indicator of gained nickel oxide powder is as follows after sieving:
Ni content 74.5%
Foreign matter content K20 Na70 Ca100 Fe100
(ppm) Al50 Si200 Cu70 Pb10
Fisher particle size 0.8 μ m
Thing phase α-NiO is a main body
Grain fineness number 370
Nickel oxide powder in the present embodiment is applicable to the dopant material of making ZnO varistor.
Claims (2)
1. the production method of a used in electronic industry cobalt oxide, nickel oxide powder, processing step comprises:
(1) cobalt salt, nickel salt solution preparation,
(2) ammonium oxalate preparation, the pH value is controlled at 2.0～5.0,
(3) cobalt oxalate, nickelous oxalate are produced in precipitin reaction, and entire reaction is under agitation carried out,
(4) filter, wash, the pH value of last elutant is controlled at 5.0～7.0,
(5) roasting cobalt oxalate, nickelous oxalate are produced cobalt oxide, nickel oxide powder, and maturing temperature is 300～500 ℃, it is characterized in that:
(1) cobalt salt, nickel salt solution are Xiao Suangu, nickel nitrate solution, and highly purified electrolytic metal cobalt, metallic nickel are made with nitric acid dissolve, and the cobalt contents in the solution, nickel content are controlled at 100～300 grams per liters, and free acid is controlled at below 10 grams per liters,
(2) during precipitin reaction, the temperature of Xiao Suangu, nickel nitrate solution is 30～50 ℃, and the add-on of ammonium oxalate determines that by endpoint pH endpoint pH is 0.5～2.5, and the reaction times is 15～30 minutes.
2. production method according to claim 1 is characterized in that roasting is directly will wash good cobalt oxalate, nickelous oxalate to carry out roasting, need not lead to oxygen during roasting, and roasting time is 4～5 hours.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB941118207A CN1163416C (en) | 1994-07-02 | 1994-07-02 | Method for producing cobalt oxide nickel oxide powder for electronic industry |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB941118207A CN1163416C (en) | 1994-07-02 | 1994-07-02 | Method for producing cobalt oxide nickel oxide powder for electronic industry |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1114639A CN1114639A (en) | 1996-01-10 |
| CN1163416C true CN1163416C (en) | 2004-08-25 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB941118207A Expired - Fee Related CN1163416C (en) | 1994-07-02 | 1994-07-02 | Method for producing cobalt oxide nickel oxide powder for electronic industry |
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Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1036707C (en) * | 1994-11-26 | 1997-12-17 | 刘宝峰 | Process for producing cobalt oxalate |
| CN1060530C (en) * | 1996-08-02 | 2001-01-10 | 潘同汉 | Method for recovery of cobalt salt with wbolt sulfonate slag of electrolytic zinc plant |
| CN1046051C (en) * | 1996-12-14 | 1999-10-27 | 中国科学院新疆物理研究所 | Oxidate semiconductor thermosensitive resistance and mfg. method thereof |
| CN1302999C (en) * | 2004-06-03 | 2007-03-07 | 曾福兴 | Method for manufacturing high-density cobaltosic oxide |
| CN1331761C (en) * | 2005-05-13 | 2007-08-15 | 中南大学 | Solid phase interface induced precipitation method for preparing nickel oxide, cobalt oxide powder |
| CN100345762C (en) * | 2005-05-18 | 2007-10-31 | 中国石油化工股份有限公司 | Nano transitional metallic oxide preparation method |
| CN1931727B (en) * | 2006-09-29 | 2010-09-08 | 自贡金丰新材料科技有限公司 | Production process of subnanometer level cobalt oxide |
| CN101066781B (en) * | 2007-06-04 | 2010-11-03 | 仙桃市中星电子材料有限公司 | Process of preparing cobalto-cobaltic oxide for lithium ion cell |
| CN101700913B (en) * | 2009-11-17 | 2011-05-18 | 中南民族大学 | Method for preparing high-purity cobalt nitrate by utilizing alumina-supported cobalt-based spent catalyst for Fischer-Tropsch synthesis |
| CN102120259B (en) * | 2011-01-28 | 2012-11-07 | 广州有色金属研究院 | Preparation method of equimolar Ti/Ni coated composite powder with nuclear shell structure |
| CN102531880A (en) * | 2012-01-04 | 2012-07-04 | 金川集团有限公司 | Preparation method of spherical nickel oxalate |
| CN102616866A (en) * | 2012-03-29 | 2012-08-01 | 金川集团有限公司 | Preparation method of porous spherical nickel oxide powder |
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1994
- 1994-07-02 CN CNB941118207A patent/CN1163416C/en not_active Expired - Fee Related
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