CN107879722A - Small electronic ceramics of a kind of rate of change of capacitance and preparation method thereof - Google Patents
Small electronic ceramics of a kind of rate of change of capacitance and preparation method thereof Download PDFInfo
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- CN107879722A CN107879722A CN201711224934.3A CN201711224934A CN107879722A CN 107879722 A CN107879722 A CN 107879722A CN 201711224934 A CN201711224934 A CN 201711224934A CN 107879722 A CN107879722 A CN 107879722A
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- 239000000919 ceramic Substances 0.000 title claims abstract description 35
- 230000008859 change Effects 0.000 title claims abstract description 29
- 238000002360 preparation method Methods 0.000 title claims abstract description 16
- 239000004927 clay Substances 0.000 claims abstract description 39
- 239000000843 powder Substances 0.000 claims abstract description 29
- 239000002994 raw material Substances 0.000 claims abstract description 25
- 235000015895 biscuits Nutrition 0.000 claims abstract description 17
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000002002 slurry Substances 0.000 claims abstract description 14
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims abstract description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 7
- HNQGTZYKXIXXST-UHFFFAOYSA-N calcium;dioxido(oxo)tin Chemical compound [Ca+2].[O-][Sn]([O-])=O HNQGTZYKXIXXST-UHFFFAOYSA-N 0.000 claims abstract description 7
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 7
- 239000011777 magnesium Substances 0.000 claims abstract description 7
- 229910052749 magnesium Inorganic materials 0.000 claims abstract description 7
- QGLKJKCYBOYXKC-UHFFFAOYSA-N nonaoxidotritungsten Chemical compound O=[W]1(=O)O[W](=O)(=O)O[W](=O)(=O)O1 QGLKJKCYBOYXKC-UHFFFAOYSA-N 0.000 claims abstract description 7
- MMKQUGHLEMYQSG-UHFFFAOYSA-N oxygen(2-);praseodymium(3+) Chemical compound [O-2].[O-2].[O-2].[Pr+3].[Pr+3] MMKQUGHLEMYQSG-UHFFFAOYSA-N 0.000 claims abstract description 7
- 229910003447 praseodymium oxide Inorganic materials 0.000 claims abstract description 7
- 229910010271 silicon carbide Inorganic materials 0.000 claims abstract description 7
- 229920005573 silicon-containing polymer Polymers 0.000 claims abstract description 7
- 239000004408 titanium dioxide Substances 0.000 claims abstract description 7
- 229910001930 tungsten oxide Inorganic materials 0.000 claims abstract description 7
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 claims abstract description 7
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 6
- RGPUVZXXZFNFBF-UHFFFAOYSA-K diphosphonooxyalumanyl dihydrogen phosphate Chemical compound [Al+3].OP(O)([O-])=O.OP(O)([O-])=O.OP(O)([O-])=O RGPUVZXXZFNFBF-UHFFFAOYSA-K 0.000 claims abstract description 6
- 239000010445 mica Substances 0.000 claims abstract description 6
- 229910052618 mica group Inorganic materials 0.000 claims abstract description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 6
- 238000010792 warming Methods 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 11
- 230000008569 process Effects 0.000 claims description 11
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 10
- 238000009413 insulation Methods 0.000 claims description 10
- 239000002245 particle Substances 0.000 claims description 10
- 238000010438 heat treatment Methods 0.000 claims description 8
- 238000005245 sintering Methods 0.000 claims description 7
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 6
- 229920002367 Polyisobutene Polymers 0.000 claims description 5
- 238000007605 air drying Methods 0.000 claims description 5
- 238000001035 drying Methods 0.000 claims description 5
- 238000000227 grinding Methods 0.000 claims description 5
- 239000012188 paraffin wax Substances 0.000 claims description 5
- 238000003756 stirring Methods 0.000 claims description 5
- 238000001291 vacuum drying Methods 0.000 claims description 5
- 239000000395 magnesium oxide Substances 0.000 claims description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 claims 2
- 229910052938 sodium sulfate Inorganic materials 0.000 claims 1
- 235000011152 sodium sulphate Nutrition 0.000 claims 1
- 239000000203 mixture Substances 0.000 abstract description 4
- 239000012776 electronic material Substances 0.000 abstract description 2
- 229910052570 clay Inorganic materials 0.000 abstract 1
- 230000004048 modification Effects 0.000 description 6
- 238000012986 modification Methods 0.000 description 6
- 239000000463 material Substances 0.000 description 4
- 229910010293 ceramic material Inorganic materials 0.000 description 3
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 3
- 229940043264 dodecyl sulfate Drugs 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 238000000498 ball milling Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000000686 essence Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- IIQJBVZYLIIMND-UHFFFAOYSA-J potassium;antimony(3+);2,3-dihydroxybutanedioate Chemical compound [K+].[Sb+3].[O-]C(=O)C(O)C(O)C([O-])=O.[O-]C(=O)C(O)C(O)C([O-])=O IIQJBVZYLIIMND-UHFFFAOYSA-J 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- AEZNLERWSLVVOK-UHFFFAOYSA-N strontium barium(2+) niobium(5+) oxygen(2-) Chemical compound [O-2].[Nb+5].[Sr+2].[Ba+2] AEZNLERWSLVVOK-UHFFFAOYSA-N 0.000 description 1
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Abstract
The invention discloses small electronic ceramics of a kind of rate of change of capacitance and preparation method thereof, it is related to technical field of electronic materials, the electronic ceramics includes following raw material:Modified clay, titanium dioxide, zirconium silicate, yittrium oxide, tungsten oxide, carborundum, mica powder, dimethyl silicone polymer, aluminium dihydrogen phosphate, praseodymium oxide, calcium stannate, magnesium titanate and Ludox.Its preparation method is that raw material first is made into powder;Add water to mix and mix to obtain high fluidity slurry;Then by slurry inject mould in curing and demolding it is dry biscuit;Finally by being heated to biscuit, the processing such as sinter.The electronic ceramics of the present invention prepares simple and convenient, low raw-material cost, has good heat-resisting quantity, and with the rise of temperature, rate of change of capacitance is small and stablizes, and dielectric loss is low, service life length, suitable popularization and application.
Description
Technical field
The present invention relates to technical field of electronic materials, and in particular to a kind of small electronic ceramics of rate of change of capacitance and its preparation
Method.
Background technology
One kind that electron ceramic material is primarily referred to as has the ceramics of the functions such as electromagnetism, its dielectric properties and electric conductivity
Adjustable range is wider, is one of material most active in special ceramic material, is widely paid close attention to by people.It can be applied in electricity
Son, communicate, automatically control, information computer, automobile, among the various fields such as aviation, there is significant social benefit and economy
Benefit.The development of Current electronic information is more and more rapider, the also more and more higher of the requirement to electronic component, miniaturization, filming,
Multi-functional grade turns into the direction of future development, and electronic ceramics product has the problem of heat-resisting quantity deficiency at present, causes its Jie
Electrical loss is big, and rate of change of capacitance is big and unstable, has a strong impact on the use of electronic ceramics product, therefore, it is necessary to improve.
The content of the invention
For problems of the prior art, the invention provides a kind of small electronic ceramics of rate of change of capacitance and its system
Preparation Method, this kind of electronic ceramics prepare simple and convenient, low raw-material cost, have good heat-resisting quantity, with the rise of temperature,
Rate of change of capacitance is small and stablizes, and dielectric loss is low, service life length, suitable popularization and application.
In order to achieve the above object, the present invention is achieved through the following technical solutions:
A kind of small electronic ceramics of rate of change of capacitance, including following raw material by weight:Modified clay 30-50 parts,
Titanium dioxide 15-25 parts, zirconium silicate 10-20 parts, yittrium oxide 8-12 parts, tungsten oxide 4-8 parts, carborundum 1-5 parts, mica powder 1-3
Part, dimethyl silicone polymer 6-10 parts, aluminium dihydrogen phosphate 8-12 parts, praseodymium oxide 3-7 parts, calcium stannate 2-6 parts, magnesium titanate 3-5 parts
With Ludox 4-8 parts;
Above-mentioned modification clay is made by following steps:Clay is first calcined 2-3h at 380-420 DEG C, then uses 8-
12% hydrochloric acid solution soaks 1-2h, then is washed with deionized to neutrality, drying, adds afterwards equivalent to clay weight 2-4%
Sldium lauryl sulfate, the chlorinated paraffin equivalent to clay weight 1-3%, the polyisobutene equivalent to clay weight 2-4% and
It is agitated to mix, dry, being crushed to powder of the particle diameter less than or equal to 500 μm i.e. equivalent to clay weight 3-5% magnesia powders
.
Further, above-mentioned electronic ceramics includes following raw material by weight:Modified 40 parts of clay, titanium dioxide
20 parts, 15 parts of zirconium silicate, 10 parts of yittrium oxide, 6 parts of tungsten oxide, 3 parts of carborundum, 2 parts of mica powder, 8 parts of dimethyl silicone polymer, phosphorus
6 parts of 10 parts of acid dihydride aluminium, 5 parts of praseodymium oxide, 4 parts of calcium stannate, 4 parts of magnesium titanate and Ludox.
A kind of preparation method of the small electronic ceramics of above-mentioned rate of change of capacitance, is followed the steps below:
(1) raw material is weighed by weight ratio, and all raw materials are mixed and made into powder;
(2) its weight 20-30% magnetized water is added in the powder, stirs and evenly mixs to obtain high fluidity slurry;
(3) slurry is injected in mould, mould is then positioned over curing process in air drying cabinet, curing and demolding obtains
To wet base, wet base is placed in vacuum drying chamber and is dried to obtain biscuit;
(4) biscuit is heated in ventilating air stove, is cooled to room temperature with air furnace afterwards;
(5) biscuit after step (4) processing is placed in sintering furnace and be sintered, be finally air-cooled to room temperature i.e.
Can.
Further, in step (1), the raw material is to obtain powder to particle diameter≤1mm by ball mill grinding.
Further, in step (2), the viscosity of the high fluidity slurry is 70-80mPas.
Further, in step (3), the curing process is to be warming up to 360-420 with 20-30 DEG C/min heating rates
DEG C, 40-50min is incubated afterwards to be terminated.
Further, in step (4), the heating is that furnace temperature first is risen into 180 DEG C~220 DEG C, then is incubated 20-
30min, it is warming up to 380 DEG C~460 DEG C again afterwards, insulation 30-40min terminates.
Further, in step (5), the sintering processes are that furnace temperature first is risen into 580 DEG C~720 DEG C, are incubated 25-
35min, then 740 DEG C~980 DEG C are warming up to, insulation 40-60min terminates.
The present invention has following beneficial effect:
(1) electrotechnical ceramics of the invention is prepared simple and convenient, and the technological process of production is safe, easy, reliable, and it processes raw material
Wide material sources, low production cost, suitable large-scale mass production;
(2) electrotechnical ceramics finished-product material of the invention is by by niobium oxide strontium barium, modified diatom powder and potassium antimony tartrate etc.
The addition of raw material, and their batch mixings, ball milling, slurrying, solidification, heat treatment, sinter molding etc. are operated so as to obtain, this kind of electricity
The ceramic material of son possesses preferable temperature stabilization performance, high temperature resistant, corrosion-resistant, its compression strength and the high service life length of tensile strength
Long, application field is extensive, has wide market prospects;
(3) insulaion resistance of electrotechnical ceramics material of the invention is big, percentage of capacitance variation with temperature is small, elongation at break is high, tool
Its insulaion resistance of body is 1.4-1.6 × 1010Ω cm, percentage of capacitance variation with temperature are 3-5ppm/ DEG C, elongation at break 150-
170%, dielectric loss is small (dielectric loss is less than 0.5%).
Embodiment
The embodiment of the present invention is further described with reference to embodiment, following examples are only used for more
Clearly demonstrate technical scheme, and can not be limited the scope of the invention with this.
Embodiment 1
A kind of small electronic ceramics of rate of change of capacitance, following raw material is weighed, it is as shown in table 1 below:
Table 1
Component | Weight (kg) |
Modified clay | 30kg |
Titanium dioxide | 15kg |
Zirconium silicate | 10kg |
Yittrium oxide | 8kg |
Tungsten oxide | 4kg |
Carborundum | 1kg |
Mica powder | 1kg |
Dimethyl silicone polymer | 6kg |
Aluminium dihydrogen phosphate | 8kg |
Praseodymium oxide | 3kg |
Calcium stannate | 2kg |
Magnesium titanate | 3kg |
Ludox | 4kg |
Above-mentioned modification clay is made by following steps:Clay is first calcined 2h at 380 DEG C, then it is molten with 8% hydrochloric acid
Liquid soaks 1h, then is washed with deionized to neutrality, drying, add afterwards the sldium lauryl sulfate equivalent to clay weight 2%,
Chlorinated paraffin equivalent to clay weight 1%, the polyisobutene equivalent to clay weight 2% and equivalent to the oxygen of clay weight 3%
Change magnesium powder, it is agitated to mix, dry, being crushed to changing needed for the i.e. obtained raw material of the present invention of powder of the particle diameter less than or equal to 500 μm
Property clay.
A kind of preparation method of the small electronic ceramics of above-mentioned rate of change of capacitance, is followed the steps below:
(1) the above-mentioned all raw materials weighed are mixed by ball mill grinding to particle diameter≤1mm, obtains powder;
(2) magnetized water of its weight 20% is added into above-mentioned powder again, stir and evenly mix viscosity is 70mPas slurries;
(3) slurry is injected in mould after, mould is positioned in air drying cabinet with 20 DEG C/min heating rate liters
Temperature is incubated 40min and terminated, above-mentioned curing process is stripped after terminating and obtains wet base, and wet base is placed in into vacuum drying afterwards to 360 DEG C
It is dried in case to obtain biscuit;
(4) by biscuit in ventilating air stove, furnace temperature is first risen to 180 DEG C, then is incubated 20min, is warming up to 380 again afterwards
DEG C, insulation 30min terminates, and is cooled to room temperature with air furnace afterwards;
(5) biscuit after step (4) processing is placed in sintering furnace, furnace temperature is first risen to 580 DEG C, be incubated 25min, then
740 DEG C are warming up to, insulation 40min terminates, and is finally air-cooled to the small electronic ceramics of the rate of change of capacitance of the i.e. obtained present invention of room temperature.
Embodiment 2
A kind of small electronic ceramics of rate of change of capacitance, following raw material is weighed, it is as shown in table 2 below:
Table 2
Component | Weight (kg) |
Modified clay | 40kg |
Titanium dioxide | 20kg |
Zirconium silicate | 15kg |
Yittrium oxide | 10kg |
Tungsten oxide | 6kg |
Carborundum | 3kg |
Mica powder | 2kg |
Dimethyl silicone polymer | 8kg |
Aluminium dihydrogen phosphate | 10kg |
Praseodymium oxide | 5kg |
Calcium stannate | 4kg |
Magnesium titanate | 4kg |
Ludox | 6kg |
Above-mentioned modification clay is made by following steps:Clay is first calcined 2.5h at 400 DEG C, then with 10% hydrochloric acid
Solution soaks 1.5h, then is washed with deionized to neutrality, drying, adds the laruyl alcohol sulphur equivalent to clay weight 3% afterwards
Sour sodium, the chlorinated paraffin equivalent to clay weight 2%, the polyisobutene equivalent to clay weight 3% and equivalent to clay weight
4% magnesia powder, it is agitated to mix, dry, being crushed to needed for the i.e. obtained raw material of the present invention of powder of the particle diameter less than or equal to 500 μm
Modification clay.
A kind of preparation method of the small electronic ceramics of above-mentioned rate of change of capacitance, is followed the steps below:
(1) the above-mentioned all raw materials weighed are mixed by ball mill grinding to particle diameter≤1mm, obtains powder;
(2) magnetized water of its weight 25% is added into above-mentioned powder again, stir and evenly mix viscosity is 75mPas slurries;
(3) slurry is injected in mould after, mould is positioned in air drying cabinet with 25 DEG C/min heating rate liters
Temperature is incubated 45min and terminated, above-mentioned curing process is stripped after terminating and obtains wet base, and wet base is placed in into vacuum drying afterwards to 390 DEG C
It is dried in case to obtain biscuit;
(4) by biscuit in ventilating air stove, furnace temperature is first risen to 200 DEG C, then is incubated 25min, is warming up to 420 again afterwards
DEG C, insulation 35min terminates, and is cooled to room temperature with air furnace afterwards;
(5) biscuit after step (4) processing is placed in sintering furnace, furnace temperature is first risen to 650 DEG C, be incubated 30min, then
850 DEG C are warming up to, insulation 50min terminates, and is finally air-cooled to the small electronic ceramics of the rate of change of capacitance of the i.e. obtained present invention of room temperature.
Embodiment 3
A kind of small electronic ceramics of rate of change of capacitance, following raw material is weighed, it is as shown in table 3 below:
Table 3
Above-mentioned modification clay is made by following steps:Clay is first calcined 3h at 420 DEG C, then it is molten with 12% hydrochloric acid
Liquid soaks 2h, then is washed with deionized to neutrality, drying, add afterwards the sldium lauryl sulfate equivalent to clay weight 4%,
Chlorinated paraffin equivalent to clay weight 3%, the polyisobutene equivalent to clay weight 4% and equivalent to the oxygen of clay weight 5%
Change magnesium powder, it is agitated to mix, dry, being crushed to changing needed for the i.e. obtained raw material of the present invention of powder of the particle diameter less than or equal to 500 μm
Property clay.
A kind of preparation method of the small electronic ceramics of above-mentioned rate of change of capacitance, is followed the steps below:
(1) the above-mentioned all raw materials weighed are mixed by ball mill grinding to particle diameter≤1mm, obtains powder;
(2) magnetized water of its weight 30% is added into above-mentioned powder again, stir and evenly mix viscosity is 80mPas slurries;
(3) slurry is injected in mould after, mould is positioned in air drying cabinet with 30 DEG C/min heating rate liters
Temperature is incubated 50min and terminated, above-mentioned curing process is stripped after terminating and obtains wet base, and wet base is placed in into vacuum drying afterwards to 420 DEG C
It is dried in case to obtain biscuit;
(4) by biscuit in ventilating air stove, furnace temperature is first risen to 220 DEG C, then is incubated 30min, is warming up to 460 again afterwards
DEG C, insulation 40min terminates, and is cooled to room temperature with air furnace afterwards;
(5) biscuit after step (4) processing is placed in sintering furnace, furnace temperature is first risen to 720 DEG C, be incubated 35min, then
980 DEG C are warming up to, insulation 60min terminates, and is finally air-cooled to the small electronic ceramics of the rate of change of capacitance of the i.e. obtained present invention of room temperature.
Performance detection
Heat-resisting quantity, insulaion resistance, percentage of capacitance variation with temperature, disconnected is carried out to electronic ceramics made from above-described embodiment 1-3
The detection of elongation and dielectric loss correlated performance is split, is recorded in table 4 below;
Table 4
The preferred embodiments of the present invention are the foregoing is only, are not intended to limit the invention, although with reference to foregoing reality
Apply example the present invention is described in detail, for those skilled in the art, it still can be to foregoing each implementation
Technical scheme described in example is modified, or carries out equivalent substitution to which part technical characteristic.All essences in the present invention
God any modification, equivalent substitution and improvements made etc., should be included in the scope of the protection with principle.
Claims (8)
1. the small electronic ceramics of a kind of rate of change of capacitance, it is characterised in that including following raw material by weight:Modified clay
30-50 parts, titanium dioxide 15-25 parts, zirconium silicate 10-20 parts, yittrium oxide 8-12 parts, tungsten oxide 4-8 parts, carborundum 1-5 parts, cloud
Female powder 1-3 parts, dimethyl silicone polymer 6-10 parts, aluminium dihydrogen phosphate 8-12 parts, praseodymium oxide 3-7 parts, calcium stannate 2-6 parts, metatitanic acid
Magnesium 3-5 parts and Ludox 4-8 parts;
The modified clay is made by following steps:Clay is first calcined 2-3h at 380-420 DEG C, then with 8-12% hydrochloric acid
Solution soaks 1-2h, then is washed with deionized to neutrality, drying, adds the laruyl alcohol equivalent to clay weight 2-4% afterwards
Sodium sulphate, the chlorinated paraffin equivalent to clay weight 1-3%, the polyisobutene equivalent to clay weight 2-4% and equivalent to pottery
Native weight 3-5% magnesia powders, it is agitated to mix, dry, being crushed to particle diameter and produced less than or equal to 500 μm of powder.
A kind of 2. small electronic ceramics of rate of change of capacitance according to claim 1, it is characterised in that including it is following by weight
The raw material of part meter:Modified 40 parts of clay, 20 parts of titanium dioxide, 15 parts of zirconium silicate, 10 parts of yittrium oxide, 6 parts of tungsten oxide, carborundum 3
Part, 2 parts of mica powder, 8 parts of dimethyl silicone polymer, 10 parts of aluminium dihydrogen phosphate, 5 parts of praseodymium oxide, 4 parts of calcium stannate, 4 parts of magnesium titanate and
6 parts of Ludox.
3. a kind of preparation method of the small electronic ceramics of rate of change of capacitance as described in claim 1-2 any one, its feature
It is, comprises the following steps:
(1) raw material is weighed by weight ratio, and all raw materials are mixed and made into powder;
(2) its weight 20-30% magnetized water is added in the powder, stirs and evenly mixs to obtain high fluidity slurry;
(3) slurry is injected in mould, mould is then positioned over curing process in air drying cabinet, curing and demolding obtains wet
Base, wet base is placed in vacuum drying chamber and is dried to obtain biscuit;
(4) biscuit is heated in ventilating air stove, is cooled to room temperature with air furnace afterwards;
(5) biscuit after step (4) processing is placed in sintering furnace and be sintered, be finally air-cooled to room temperature.
4. the preparation method of the small electronic ceramics of a kind of rate of change of capacitance according to claim 3, it is characterised in that in step
Suddenly in (1), the raw material is to obtain powder to particle diameter≤1mm by ball mill grinding.
5. the preparation method of the small electronic ceramics of a kind of rate of change of capacitance according to claim 3, it is characterised in that in step
Suddenly in (2), the viscosity of the high fluidity slurry is 70-80mPas.
6. the preparation method of the small electronic ceramics of a kind of rate of change of capacitance according to claim 3, it is characterised in that in step
Suddenly in (3), the curing process is to be warming up to 360-420 DEG C with 20-30 DEG C/min heating rates, is incubated 40-50min knots afterwards
Beam.
7. the preparation method of the small electronic ceramics of a kind of rate of change of capacitance according to claim 3, it is characterised in that in step
Suddenly in (4), the heating is that furnace temperature first is risen into 180 DEG C~220 DEG C, then is incubated 20-30min, is warming up to 380 again afterwards
DEG C~460 DEG C, insulation 30-40min terminates.
8. the preparation method of the small electronic ceramics of a kind of rate of change of capacitance according to claim 3, it is characterised in that in step
Suddenly in (5), the sintering processes are that furnace temperature first risen into 580 DEG C~720 DEG C, are incubated 25-35min, then be warming up to 740 DEG C~
980 DEG C, insulation 40-60min terminates.
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CN112919884A (en) * | 2019-12-05 | 2021-06-08 | 湖南创安防爆电器有限公司 | Explosion-proof ceramic material and preparation method thereof |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4992399A (en) * | 1987-06-23 | 1991-02-12 | Canon Kabushiki Kaisha | Ceramic, circuit substrate and electronic circuit substrate by use thereof and process for producing ceramic |
CN102969153A (en) * | 2012-10-31 | 2013-03-13 | 安徽拓普森电池有限责任公司 | Capacitor impregnant containing modified sepiolite powder and preparation method thereof |
CN106116535A (en) * | 2016-06-22 | 2016-11-16 | 赣州艺佳兴陶瓷有限公司 | A kind of multifunctional ceramic material and preparation technology thereof |
CN106927785A (en) * | 2017-03-24 | 2017-07-07 | 合肥羿振电力设备有限公司 | A kind of manufacture craft of power equipment insulating ceramics |
CN107176833A (en) * | 2017-07-04 | 2017-09-19 | 合肥择浚电气设备有限公司 | A kind of high temperature resistant electrical ceramics and preparation method thereof |
-
2017
- 2017-11-29 CN CN201711224934.3A patent/CN107879722A/en active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4992399A (en) * | 1987-06-23 | 1991-02-12 | Canon Kabushiki Kaisha | Ceramic, circuit substrate and electronic circuit substrate by use thereof and process for producing ceramic |
CN102969153A (en) * | 2012-10-31 | 2013-03-13 | 安徽拓普森电池有限责任公司 | Capacitor impregnant containing modified sepiolite powder and preparation method thereof |
CN106116535A (en) * | 2016-06-22 | 2016-11-16 | 赣州艺佳兴陶瓷有限公司 | A kind of multifunctional ceramic material and preparation technology thereof |
CN106927785A (en) * | 2017-03-24 | 2017-07-07 | 合肥羿振电力设备有限公司 | A kind of manufacture craft of power equipment insulating ceramics |
CN107176833A (en) * | 2017-07-04 | 2017-09-19 | 合肥择浚电气设备有限公司 | A kind of high temperature resistant electrical ceramics and preparation method thereof |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112919884A (en) * | 2019-12-05 | 2021-06-08 | 湖南创安防爆电器有限公司 | Explosion-proof ceramic material and preparation method thereof |
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