Patent Application
20210053840
The disclosure relates to a co-current co-precipitation method of CoNiO2 thermistor powders, and particularly relates to a preparation method of a semi-conductor nano material.
A negative temperature coefficient (NTC) thermistor refers to a material whose resistance value decreases exponentially with the increase of the temperature within the range of working temperature. It, especially, a CoNiO2 NTC thermal-sensitive material with high b value, low resistivity and good thermal stability, plays an important role in the fields of military, aerospace, home appliances, automobiles and the like. With the continuous development of theoretical researches and preparation technologies, all of the electrical property, thermal stability and repeatability of the material have been greatly improved. At present, it is urgent to need NTC thermistors and infrared detectors with higher precision, faster response and better stability in the civil industry and aerospace industry. Therefore, there are increasing requirements for the output and quality of thermistors.
Preparation of powders is the most crucial step for the preparation of a thermistor element. Nano-scale powder has high reaction activity, which obviously improves the consistency of B value and resistance value of the NTC thermistor, and greatly improves the interchangeability of elements. The researches prove that uniform particle size distribution and appropriate granularity directly affect the electrical property, stability and consistency of the NTC thermistor. On the one hand, preparation and synthesis of nano NTC thermistor powders can improve the performance of the existing bulk element, and on the other hand, it has far-reaching significance for the preparation of micro NTC thermistor elements.
At present, the methods involved in the existing technology are either complex in operation and high in experimental requirements, or complex in process, high in equipment requirements, difficult to operate and low in industrial application value. In order to solve the problems existing in the prior art, the disclosure adopts a co-current co-precipitation method to prepare nano CoNiO2 powders.
At the same time, Co ions in the CoNiO2 powders are extremely easily oxidized in the process of calcination, which makes it become a difficult point in the process of powders manufacturing. During the calcination process, we ensure that the obtained nano material is stable in property and not easy to oxidize by introducing inert atmosphere argon for protection and strictly controlling calcination temperature-rising rate and calcination temperature and other process parameters as well as calcination atmosphere.
The objective of the disclosure is to provide a co-current co-precipitation method of CoNiO2 thermistor powders and prepare the CoNiO2 thermistor powders into a high-precision, fast-response and small-volume temperature sensor material. The method comprises the steps of mixing, stirring, precipitating, aging, suction filtration, washing and drying by firstly using nickel nitrate and cobalt nitrate as raw materials to obtain cobalt hydroxide, and then calcining in a tubular furnace at an inert atmosphere to prepare CoNiO2 nano powders. The method has the advantages of convenient operation, low cost, short period, high yield, no environmental pollution and the like. The CoNiO2 nano material can be avoided further oxidized into NiCo2O4 through selection and adjustment of calcination process parameters and inert atmosphere. A high-precision, fast-response and small-volume temperature sensor material can be prepared from CoNiO2 thermistor powders obtained by the method of the disclosure.
The disclosure provides a co-current co-precipitation method of CoNiO2 thermistor powders, comprising the following steps:
a, mixing raw materials Co(NO3)2 and Ni(NO3)2 in a mole ratio of 1:1, and dissolving the obtained mixture into deionized water, so as to prepare 0.5-3 mol/L mixed solution A;
b, weighing Co(NO3)2 and Ni(NO3)2 in a mole ratio of 1: (1.2-2.0), then weighing sodium hydroxide, oxalic acid, sodium carbonate, ammonium bicarbonate or ammonium hydroxide, and adding deionized water, so as to prepare 0.5-3 mol/L solution B;
c, weighing polyvinylpyrrolidone powders, polyethylene glycol 400, polyethylene glycol 600, cetyltrimethyl ammonium bromide or triton X-100 to be dissolved into deionized water, so as to prepare dispersant solution C having a mass fraction of 0.5-10%;
d, respectively putting the solution A and solution B prepared in step a and step b in a dropping funnel, simultaneously dropwise adding the solution A and the solution B into the solution C in step c at the speed of 0.5-2 drop/s at the same time, and magnetically stirring for 1-4 hours to form a precipitate;
e, standing and aging the precipitate formed in step d for 24-72 h, then carrying out suction filtration, and washing to be neutral; and
f, putting the precipitate obtained in step e into a vacuum drying oven for drying, then putting the dried precipitate into a tubular furnace, introducing inert gas argon or nitrogen, raising the temperature of the tubular furnace to 200-250° C. at the heating rate of 0.5-2° C./min, calcining at a constant temperature and preserving for 30-60 min, then heating to 300-600° C., calcining at a constant temperature and preserving for 1-4 h, cooling down to room temperature at the cooling rate of 0.5-2° C./min, calcining, and subsequently and carrying out dry ball milling for 2 h, so as to obtain the CoNiO2 thermistor powders.
The disclosure relates to a co-current co-precipitation method of CoNiO2 thermistor powders, which has been protected by inert gas throughout the calcination process from beginning to end.
The disclosure relates to the co-current co-precipitation method of CoNiO2 thermistor powders. The CoNiO2 powders synthesized by this method undergoes tabletting, sintering and electrode coating to obtain a thermistor chip, an electrode lead is subjected to spot welding, and the thermistor is tested.
The co-current co-precipitation method of CoNiO2 thermistor powders disclosed by the disclosure has the advantages:
1) The CoNiO2 powders whose molar ratio is strictly controllable can be obtained;
2) The synthesis of the CoNiO2 powders using the co-current co-precipitation method has the advantages of simple operation, low cost, high yield, short generation cycle and the like, and this method is easy for industrial production;
3) The further oxidation process from the CoNiO2 nano material into NiCo2O4 can be effectively avoided through selection and adjustment of calcination process parameters and inert atmosphere.
a, raw materials Co(NO3)2 and Ni(NO3)2 were mixed in a mole ratio of 1:1, and dissolved into deionized water, so as to prepare 0.5 mol/L mixed solution A;
b, Co(NO3)2 and Ni(NO3)2 were weighed in a mole ratio of 1:1.2, then sodium hydroxide was weighed, and deionized water was added, so as to prepare 0.5 mol/L solution B;
c, polyvinylpyrrolidone powders was weighed as a dispersant and dissolved into deionized water, so as to prepare dispersant solution C having a mass fraction of 0.5%;
d, the solution A and solution B prepared in step a and step b were respectively put in a dropping funnel, simultaneously dropwise added into the solution C in step c at the speed of 0.5 drop/s, and magnetically stirred for 1 hour to form a precipitate;
e, the precipitate formed in step d was stood and aged for 24 h, then subjected to suction filtration, and washed to be neutral; and
f, the precipitate obtained in step e was put into a vacuum drying oven for drying, then put into a tubular furnace, inert gas argon or nitrogen was introduced, the temperature of the tubular furnace was raised to 200° C. at the heating rate of 0.5° C./min, calcination was carried out at a constant temperature and preservation was performed for 30 min, then the temperature was raised to 300° C., then calcination was carried out at a constant temperature and preservation was performed for 1 h, the temperature was reduced to room temperature at the cooling rate of 0.5° C./min, calcinination was carried out, and subsequently dry ball milling was carried out for 2 h, so as to obtain the CoNiO2 thermistor powders. The whole calcination process was protected by inert gas from beginning to end.
a, raw materials Co(NO3)2 and Ni(NO3)2 were mixed in a mole ratio of 1:1, and dissolved into deionized water, so as to prepare 1 mol/L mixed solution A;
b, Co(NO3)2 and Ni(NO3)2 were weighed in a mole ratio of 1:1.4, then oxalic acid was weighed, and deionized water was added, so as to prepare 1 mol/L solution B;
c, polyethylene glycol 400 was weighed as a dispersant and dissolved into deionized water, so as to prepare dispersant solution C having a mass fraction of 2%;
d, the solution A and solution B prepared in step a and step b were respectively put in a dropping funnel, simultaneously dropwise added into the solution C in step c at the speed of 1 drop/s, and magnetically stirred for 2 h to form a precipitate;
e, the precipitate formed in step d was stood and aged for 36 h, then subjected to suction filtration, and washed to be neutral; and
f, the precipitate obtained in step e was put into a vacuum drying oven for drying, then put into a tubular furnace, inert gas argon or nitrogen was introduced, the temperature of the tubular furnace was raised to 210° C. at the heating rate of 1° C./min, calcination was carried out at a constant temperature and preservation was performed for 40 min, then the temperature was raised to 400° C., then calcination was carried out at a constant temperature and preservation was performed for 2 h, the temperature was reduced to room temperature at the cooling rate of 1° C./min, calcinination was carried out, and subsequently dry ball milling was carried out for 2 h, so as to obtain the CoNiO2 thermistor powders. The whole calcination process was protected by inert gas from beginning to end.
a, raw materials Co(NO3)2 and Ni(NO3)2 were mixed in a mole ratio of 1:1, and dissolved into deionized water, so as to prepare 1.5 mol/L mixed solution A;
b, Co(NO3)2 and Ni(NO3)2 were weighed in a mole ratio of 1:1.6, then sodium carbonate was weighed, and deionized water was added, so as to prepare 1.5 mol/L solution B;
c, polyethylene glycol 600 was weighed as a dispersant and dissolved into deionized water, so as to prepare dispersant solution C having a mass fraction of 4%;
d, the solution A and solution B prepared in step a and step b were respectively put in a dropping funnel, simultaneously dropwise added into the solution C in step c at the speed of 1 drop/s, and magnetically stirred for 2 h to form a precipitate;
e, the precipitate formed in step d was stood and aged for 48 h, then subjected to suction filtration, and washed to be neutral; and
f, the precipitate obtained in step e was put into a vacuum drying oven for drying, then put into a tubular furnace, inert gas argon or nitrogen was introduced, the temperature of the tubular furnace was raised to 220° C. at the heating rate of 1° C./min, calcination was carried out at a constant temperature and preservation was performed for 40 min, then the temperature was raised to 400° C., then calcination was carried out at a constant temperature and preservation was performed for 2 h, the temperature was reduced to room temperature at the cooling rate of 1° C./min, calcinination was carried out, and subsequently dry ball milling was carried out for 2 h, so as to obtain the CoNiO2 thermistor powders. The whole calcination process was protected by inert gas from beginning to end.
a, raw materials Co(NO3)2 and Ni(NO3)2 were mixed in a mole ratio of 1:1, and dissolved into deionized water, so as to prepare 2 mol/L mixed solution A;
b, Co(NO3)2 and Ni(NO3)2 were weighed in a mole ratio of 1:1.8, then ammonium bicarbonate was weighed, and deionized water was added, so as to prepare 2 mol/L solution B;
c, cetyltrimethyl ammonium bromide was weighed as a dispersant and dissolved into deionized water, so as to prepare dispersant solution C having a mass fraction of 6.5%;
d, the solution A and solution B prepared in step a and step b were respectively put in a dropping funnel, simultaneously dropwise added into the solution C in step c at the speed of 1.5 drop/s, and magnetically stirred for 3 h to form a precipitate;
e, the precipitate formed in step d was stood and aged for 48 h, then subjected to suction filtration, and washed to be neutral; and
f, the precipitate obtained in step e was put into a vacuum drying oven for drying, then put into a tubular furnace, inert gas argon or nitrogen was introduced, the temperature of the tubular furnace was raised to 230° C. at the heating rate of 1.5° C./min, calcination was carried out at a constant temperature and preservation was performed for 50 min, then the temperature was raised to 500° C., then calcination was carried out at a constant temperature and preservation was performed for 3 h, the temperature was reduced to room temperature at the cooling rate of 1.5° C./min, calcinination was carried out, and subsequently dry ball milling was carried out for 2 h, so as to obtain the CoNiO2 thermistor powders. The whole calcination process was protected by inert gas from beginning to end.
a, raw materials Co(NO3)2 and Ni(NO3)2 were mixed in a mole ratio of 1:1, and dissolved into deionized water, so as to prepare 2.5 mol/L mixed solution A;
b, Co(NO3)2 and Ni(NO3)2 were weighed in a mole ratio of 1:1.8, then ammonium hydroxide was weighed, and deionized water was added, so as to prepare 2.5 mol/L solution B;
c, triton X-100 was weighed as a dispersant and dissolved into deionized water, so as to prepare dispersant solution C having a mass fraction of 8.5%;
d, the solution A and solution B prepared in step a and step b were respectively put in a dropping funnel, simultaneously dropwise added into the solution C in step c at the speed of 1.5 drop/s, and magnetically stirred for 3 h to form a precipitate;
e, the precipitate formed in step d was stood and aged for 60 h, then subjected to filtered at reduced pressure, and washed to be neutral; and
f, the precipitate obtained in step e was put into a vacuum drying oven for drying, then put into a tubular furnace, inert gas argon or nitrogen was introduced, the temperature of the tubular furnace was raised to 240° C. at the heating rate of 1.5° C./min, calcination was carried out at a constant temperature and preservation was performed for 50 min, then the temperature was raised to 500° C., then calcination was carried out at a constant temperature and preservation was carried out for 3 h, the temperature was reduced to room temperature at the cooling rate of 1.5° C./min, calcinination was carried out, and subsequently dry ball milling was carried out for 2 h, so as to obtain the CoNiO2 thermistor powders. The whole calcination process was protected by inert gas from beginning to end.
a, raw materials Co(NO3)2 and Ni(NO3)2 were mixed in a mole ratio of 1:1, and dissolved into deionized water, so as to prepare 3 mol/L mixed solution A;
b, Co(NO3)2 and Ni(NO3)2 were weighed in a mole ratio of 1:2.0, then sodium hydroxide was weighed, and deionized water was added, so as to prepare 3 mol/L solution B;
c, polyvinylpyrrolidone powders was weighed as a dispersant and dissolved into deionized water, so as to prepare dispersant solution C having a mass fraction of 10%;
d, the solution A and solution B prepared in step a and step b were respectively put in a dropping funnel, simultaneously dropwise added into the solution C in step c at the speed of 2 drop/s, and magnetically stirred for 4 h to form a precipitate;
e, the precipitate formed in step d was stood and aged for 72 h, then filtered at reduced pressure, and washed to be neutral; and
f, the precipitate obtained in step e was put into a vacuum drying oven for drying, then put into a tubular furnace, inert gas argon or nitrogen was introduced, the temperature of the tubular furnace was raised to 250° C. at the heating rate of 2° C./min, calcination was carried out at a constant temperature and preservation was performed for 60 min, then the temperature was raised to 600° C., then calcination was carried out at a constant temperature and preservation was performed for 4 h, the temperature was reduced to room temperature at the cooling rate of 2° C./min, calcinination was carried out, and subsequently dry ball milling was carried out for 2 h, so as to obtain the CoNiO2 thermistor powders. The whole calcination process was protected by inert gas from beginning to end.
The CoNiO2 thermistor powders obtained in any one of examples 1-6 were subjected to X-ray diffraction and scanning electron microscope analysis characterization. The test showed that the CoNiO2 thermistor powders obtained by the method of the disclosure all formed the CoNiO2 cubic crystal phase whose morphology was basically hexahedral nano sheets.
| Number | Date | Country | Kind |
|---|---|---|---|
| 201910764236.5 | Aug 2019 | CN | national |
