CN109202092A - A kind of technique for preparing iron sial powder using non-real air atomizing and making magnetic core - Google Patents
A kind of technique for preparing iron sial powder using non-real air atomizing and making magnetic core Download PDFInfo
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- CN109202092A CN109202092A CN201811079978.6A CN201811079978A CN109202092A CN 109202092 A CN109202092 A CN 109202092A CN 201811079978 A CN201811079978 A CN 201811079978A CN 109202092 A CN109202092 A CN 109202092A
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- powder
- magnetic core
- iron
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- air atomizing
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- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 title claims abstract description 68
- 239000000843 powder Substances 0.000 title claims abstract description 48
- 229910052742 iron Inorganic materials 0.000 title claims abstract description 34
- 238000000034 method Methods 0.000 title claims abstract description 23
- 238000000137 annealing Methods 0.000 claims abstract description 23
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 17
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims abstract description 17
- 238000000889 atomisation Methods 0.000 claims abstract description 11
- 239000000654 additive Substances 0.000 claims abstract description 10
- 230000000996 additive effect Effects 0.000 claims abstract description 10
- 238000002360 preparation method Methods 0.000 claims abstract description 10
- 229910000702 sendust Inorganic materials 0.000 claims abstract description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 16
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 14
- 238000003756 stirring Methods 0.000 claims description 14
- -1 iron aluminum silicon Chemical compound 0.000 claims description 13
- 239000011863 silicon-based powder Substances 0.000 claims description 13
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 8
- 229910052757 nitrogen Inorganic materials 0.000 claims description 8
- 239000001301 oxygen Substances 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- 230000004224 protection Effects 0.000 claims description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 7
- 229910000831 Steel Inorganic materials 0.000 claims description 7
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 7
- 229910052799 carbon Inorganic materials 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 239000000428 dust Substances 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 7
- 239000000314 lubricant Substances 0.000 claims description 7
- 239000010959 steel Substances 0.000 claims description 7
- 229910000519 Ferrosilicon Inorganic materials 0.000 claims description 6
- 229910019142 PO4 Inorganic materials 0.000 claims description 6
- 238000003801 milling Methods 0.000 claims description 6
- 239000010452 phosphate Substances 0.000 claims description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 6
- 239000011248 coating agent Substances 0.000 claims description 5
- 238000000576 coating method Methods 0.000 claims description 5
- 239000003822 epoxy resin Substances 0.000 claims description 5
- 229920000647 polyepoxide Polymers 0.000 claims description 5
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 claims description 5
- 239000004615 ingredient Substances 0.000 claims description 4
- 238000009413 insulation Methods 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- 235000012239 silicon dioxide Nutrition 0.000 claims description 4
- 239000000377 silicon dioxide Substances 0.000 claims description 4
- 239000002893 slag Substances 0.000 claims description 4
- 239000002131 composite material Substances 0.000 claims description 3
- 239000007789 gas Substances 0.000 claims description 3
- 239000006247 magnetic powder Substances 0.000 claims description 3
- 235000019353 potassium silicate Nutrition 0.000 claims description 3
- 239000002994 raw material Substances 0.000 claims description 3
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims description 3
- 239000007921 spray Substances 0.000 claims description 3
- RLQWHDODQVOVKU-UHFFFAOYSA-N tetrapotassium;silicate Chemical compound [K+].[K+].[K+].[K+].[O-][Si]([O-])([O-])[O-] RLQWHDODQVOVKU-UHFFFAOYSA-N 0.000 claims description 3
- 239000004593 Epoxy Substances 0.000 claims description 2
- 239000000853 adhesive Substances 0.000 claims description 2
- 230000001070 adhesive effect Effects 0.000 claims description 2
- 239000011230 binding agent Substances 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 229910052681 coesite Inorganic materials 0.000 claims description 2
- 229910052906 cristobalite Inorganic materials 0.000 claims description 2
- 238000001514 detection method Methods 0.000 claims description 2
- 239000012535 impurity Substances 0.000 claims description 2
- 239000003973 paint Substances 0.000 claims description 2
- 230000001681 protective effect Effects 0.000 claims description 2
- 230000035484 reaction time Effects 0.000 claims description 2
- 229910052682 stishovite Inorganic materials 0.000 claims description 2
- 229910052905 tridymite Inorganic materials 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
- 238000003723 Smelting Methods 0.000 abstract description 7
- 239000004411 aluminium Substances 0.000 abstract description 7
- 238000005516 engineering process Methods 0.000 abstract description 6
- 238000007873 sieving Methods 0.000 abstract description 6
- 238000007254 oxidation reaction Methods 0.000 abstract description 5
- 230000003647 oxidation Effects 0.000 abstract description 4
- 238000000748 compression moulding Methods 0.000 abstract description 3
- 238000012387 aerosolization Methods 0.000 description 10
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- XWHPIFXRKKHEKR-UHFFFAOYSA-N iron silicon Chemical compound [Si].[Fe] XWHPIFXRKKHEKR-UHFFFAOYSA-N 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- VAWNDNOTGRTLLU-UHFFFAOYSA-N iron molybdenum nickel Chemical compound [Fe].[Ni].[Mo] VAWNDNOTGRTLLU-UHFFFAOYSA-N 0.000 description 2
- UGKDIUIOSMUOAW-UHFFFAOYSA-N iron nickel Chemical compound [Fe].[Ni] UGKDIUIOSMUOAW-UHFFFAOYSA-N 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 238000007499 fusion processing Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910001004 magnetic alloy Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F9/00—Making metallic powder or suspensions thereof
- B22F9/02—Making metallic powder or suspensions thereof using physical processes
- B22F9/06—Making metallic powder or suspensions thereof using physical processes starting from liquid material
- B22F9/08—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying
- B22F9/082—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying atomising using a fluid
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F1/00—Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
- B22F1/10—Metallic powder containing lubricating or binding agents; Metallic powder containing organic material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F1/00—Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
- B22F1/14—Treatment of metallic powder
- B22F1/142—Thermal or thermo-mechanical treatment
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/02—Compacting only
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/24—After-treatment of workpieces or articles
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
- H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
- H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
- H01F1/12—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials
- H01F1/14—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials metals or alloys
- H01F1/147—Alloys characterised by their composition
- H01F1/14766—Fe-Si based alloys
- H01F1/14791—Fe-Si-Al based alloys, e.g. Sendust
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/24—After-treatment of workpieces or articles
- B22F2003/241—Chemical after-treatment on the surface
- B22F2003/242—Coating
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/24—After-treatment of workpieces or articles
- B22F2003/248—Thermal after-treatment
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F9/00—Making metallic powder or suspensions thereof
- B22F9/02—Making metallic powder or suspensions thereof using physical processes
- B22F9/06—Making metallic powder or suspensions thereof using physical processes starting from liquid material
- B22F9/08—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying
- B22F9/082—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying atomising using a fluid
- B22F2009/0844—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying atomising using a fluid in controlled atmosphere
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F9/00—Making metallic powder or suspensions thereof
- B22F9/02—Making metallic powder or suspensions thereof using physical processes
- B22F9/06—Making metallic powder or suspensions thereof using physical processes starting from liquid material
- B22F9/08—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying
- B22F9/082—Making metallic powder or suspensions thereof using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying atomising using a fluid
- B22F2009/0848—Melting process before atomisation
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F2998/00—Supplementary information concerning processes or compositions relating to powder metallurgy
- B22F2998/10—Processes characterised by the sequence of their steps
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- Engineering & Computer Science (AREA)
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- Manufacturing & Machinery (AREA)
- Mechanical Engineering (AREA)
- Thermal Sciences (AREA)
- Electromagnetism (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Power Engineering (AREA)
- Soft Magnetic Materials (AREA)
- Manufacture Of Metal Powder And Suspensions Thereof (AREA)
Abstract
The present invention relates to a kind of techniques for preparing iron sial powder using non-real air atomizing and making magnetic core, by adding suitable additive, and suitable smelting technology, aluminium vigorous oxidation when reducing high temperature to the greatest extent and form a large amount of clinkers, avoid that stifled furnace occurs when atomization, can continuously prepare powder, after the powder sieving of preparation, 60 sendust core 100K/100mT of μ loss 500mW/cm is realized by compression moulding and high-temperature annealing process by the high temperature anneal and insulating wrapped processing3;It is superimposed performance 100Oe:63%;50Oe:83%.
Description
Technical field
The present invention relates to a kind of preparation methods of inexpensive low-loss soft-magnetic alloy powder, refer in particular to a kind of using non-real
Air atomizing iron sial powder preparation method.
Background technique
Powder preparation is that the first step of production alloy magnetic powder core is also one of most critical, and conventional preparation method has atomization
Method, crush method etc., aerosolization is to prepare a kind of common methods of metal powder, wherein can be divided according to the difference of smelting equipment
For vacuum aerosolization and non-real air atomizing.When preparing high value powder such as iron nickel, iron nickel molybdenum, there is the use of amount of powder producer
Vacuum aerosolization mode prepares high-quality iron nickel, iron nickel molybdenum powder, is exactly when preparing aerosolization iron sial there are also one kind, due to
In iron sial fusion process can because high-temperature oxydation generates a large amount of clinkers, be very easy to obstruction atomization let slip a remark and spray gun, institute
It is prepared in a manner of frequently with vacuum melting.
Although the powder quality that vacuum aerosolization prepares is good, its equipment investment is big, and complex process causes powder
Yield is by equipment limit and cost remains high.
Although existing non-real air atomizing is advantageous on equipment capacity and cost, the powder in melting and atomization process
Oxygen content can increase in end, and as the aluminium in Aluminum steel liquid can be because with the oxygen in atmosphere reacting for fierceness, oxygen occur for high temperature
Change and generate a large amount of clinkers, the incidental serious clinker of oxidation is excessive when preparing aerosolization iron sial, and easily stifled furnace, this is gas
The normal production of atomization iron sial causes to hinder.
Summary of the invention
The object of the present invention is to provide a kind of low-loss, high superposition 60 aerosolization iron sial powder of μ and magnetic core preparation methods.
The present invention by adding suitable additive and suitable smelting technology, aluminium vigorous oxidation when reducing high temperature to the greatest extent and formed big
Clinker is measured, avoids that stifled furnace occurs when atomization, can continuously prepare powder, after the powder sieving of preparation, simultaneously by the high temperature anneal
Insulating wrapped processing realizes 60 sendust core 100K/100mT of μ loss by compression moulding and high-temperature annealing process
500mW/cm3;It is superimposed performance 100Oe:85%;50Oe:95%.
To achieve the goals above, the invention adopts the following technical scheme:
A kind of technique preparing iron sial powder using non-real air atomizing and make magnetic core, the technique the following steps are included:
1) major ingredient pure iron is taken, ferrosilicon, aluminum shot, auxiliary material is deslagging agent, carbon dust;
2) pure iron is put into intermediate frequency furnace, heated, soon melted completion to pure iron and be put into ferrosilicon, reduce frequency first after mixing evenly
Secondary fishing slag;
3) protective atmosphere gas curtain is opened after fishing out slag, pours into aluminum shot, quickly stirs and start thermometric, prepares atomization;
4) control of tundish initial temperature pours into molten steel and starts to be atomized at 1400 DEG C or more, keeps atomizing pressure;
5) it adjusts intermediate frequency furnace and Tundish Heating is kept for 1700 DEG C of molten steel temperature >, molten steel exposed part is formed during atomization and is protected
Protect atmosphere;6) sub-sieve is carried out to original powder after the completion of being atomized, rod milling and airflow milling is sold, sells rod milling again after nitrogen protection high annealing
It is stand-by that mixing is carried out afterwards;
7) it takes powder to carry out carrying out physical chemistry detection, the phosphoric acid solution being diluted with water is added;
8) iron aluminum silicon powder reacts in phosphoric acid solution, and the reaction time is 1-2 hours, after the reaction was completed in 80 DEG C~130 DEG C situations
Under be dried;
9) iron aluminum silicon powder is annealed 1-2 hours in n 2 annealing furnace high temperature again after phosphorating treatment, and temperature is higher than 500 DEG C;
10) high temperature resistant binder waterglass, potassium water glass, composite phosphate, SiO2 colloidal sol are added after the completion of the insulation of iron aluminum silicon powder
One or more of, additive amount is 0.5~2%;
11) zinc stearate is added after the completion of iron aluminum silicon powder insulation adhesive as lubricant, is mixed magnetic powder and is pressed into iron sial core magnetic
Core;
12) ferrocart core magnetic core is in N2Annealing heat-treatment is carried out under atmosphere;
13) magnetic core spray epoxy paint;
14) 500~450mW/cm is lost in the 026 sendust core 100K/100mT of μ to the preparation of top method3;It is superimposed performance
100Oe:61~63%;50Oe:80~83%.
Preferably, the mass fraction of each raw material is respectively as follows: major ingredient pure iron 80%~82%, ferrosilicon 9.5% in step 1)
~10%, aluminum shot 5%~6%, auxiliary material is deslagging agent 0.2 ‰, and carbon dust 0.5 ‰, surplus is inevitable impurity.
Preferably, the temperature of thermometric reaches 1750 DEG C~1800 DEG C in step 3), start to be atomized.
Preferably, keeping atomizing pressure in step 4) is 3.0Mpa.
Preferably, the additive amount of lubricant is the 0.2-0.5% of iron aluminum silicon powder in step 11), the pressure of compacting is
20T/cm3。
Preferably, the temperature being heat-treated in step 12) is 600-750 DEG C, when annealing Control for Oxygen Content 50ppm with
Under.
Preferably, in step 13) epoxy resin coating with a thickness of 0.3-0.5mm.
The beneficial effects of the present invention are: the present invention is subtracted as far as possible by adding suitable additive and suitable smelting technology
Aluminium vigorous oxidation when few high temperature and form a large amount of clinkers, avoid that stifled furnace occurs when atomization, can continuously prepare powder, the powder of preparation
After sieving, is handled by the high temperature anneal and insulating wrapped, by compression moulding and high-temperature annealing process, realize 60 iron of μ
500mW/cm is lost in sial magnetic core 100K/100mT3;It is superimposed performance 100Oe:63%;50Oe:83%.
Specific embodiment
The invention will be further described With reference to embodiment, following embodiment be intended to illustrate invention and
It is not limitation of the invention further, the present invention can be implemented by formula either described in summary of the invention.
To avoid repeating, first by raw material involved in present embodiment and related technological parameter Unify legislation as follows with
Under repeat no more in each embodiment.
Embodiment 1
75%Si Antaciron 9.5%, aluminum shot 5%, carbon dust 0.2 ‰, deslagging agent 0.5 ‰, surplus are taken based on mass fraction 100%
For 99.9% pure iron, aerosolization iron sial is prepared by smelting technology, selects 6.0 to let slip a remark, atomizing pressure 3.0Mpa prepares powder and goes out
Powder rate 75%, powder physical chemistry test result are shown in Table 1;
It takes 200 mesh iron aluminum silicon powder 1kg to controllable temperature agitated kettle, 30% phosphate aqueous solution 100ml is added, phosphoric acid additive amount accounts for iron silicon
Aluminium powder weight ratio 2%, after uninterrupted stirring 1 hour, stirring pot temperature rises to 120 DEG C, roasts to drying, is put into powder after sieving
2 hours of annealing furnace high annealing of nitrogen protection, high-temperature agglomerant waterglass 50g is added, continues to stir, until dry.
30g zinc stearate powdered lubricant is added, stirs evenly, by powder with 20 tons/cm3Pressure is pressed into OD27.0, ID14.8, HT11.0
Standard magnet ring, made annealing treatment under 750 DEG C of nitrogen protections, Control for Oxygen Content is in 20ppm, heat treatment when annealing
Between be 180 minutes, finally sprayed with epoxy resin coating.
Copper wire uses Φ 0.5mm, and 20 circle of coil turn is tested with HP4284 inductance analyzer in 100kHz, 1V
Inductance L and quality factor Q.Copper wire uses Φ 0.8mm, 25 circle of coil turn, with HP4284 inductance analyzer in 10kHz, 0.05V
In the case of test 0A inductance and plus 20A (i.e. 100Oe) DC stacked inductance, calculate and be superimposed percentage in 100Oe.Function
Rate loss is measured with Φ 0.5mm copper wire in such a way that 30 circles add 5 circles as a result, the μ of inductance L29.26~30.05 H, 200KhzQ value 61
~65, loss value of the power loss in 100kHz, 100mT is 466.86mW/cm3;It is superimposed performance 100Oe:62.55%;
50Oe:82.91%.
Embodiment 2
Take 75%Si Antaciron 9.8% based on mass fraction 100%, aluminum shot 5.8%, carbon dust 0.2 ‰, deslagging agent 0.5 ‰ is remaining
Amount is 99.9% pure iron, prepares aerosolization iron sial by smelting technology, selects 6.0 to let slip a remark, atomizing pressure 3.0Mpa prepares powder
Flour extraction 76%;
It takes 200 mesh iron aluminum silicon powder 1kg to controllable temperature agitated kettle, 30% phosphate aqueous solution 100ml is added, phosphoric acid additive amount accounts for iron silicon
Aluminium powder weight ratio 2%, after uninterrupted stirring 1.5 hours, stirring pot temperature rises to 80 DEG C, roasts to drying, puts powder after sieving
1000 DEG C of annealing furnace 2 hours of annealing for entering nitrogen protection, composite phosphate 25g and silicon dioxide gel 25g are added, continued
Stirring, until dry.30g zinc stearate powdered lubricant is added, stirs evenly, by powder with 20 tons/cm3Pressure is pressed into
The standard magnet ring of OD27.0, ID14.8, HT11.0, are made annealing treatment under 750 ± 5 DEG C of nitrogen protections, oxygen when annealing
In 20ppm, heat treatment time is 180 minutes for content control, is finally sprayed with epoxy resin coating.
Copper wire uses Φ 0.5mm, and 20 circle of coil turn is tested with HP4284 inductance analyzer in 100kHz, 1V
Inductance L and quality factor Q.Copper wire uses Φ 0.8mm, 25 circle of coil turn, with HP4284 inductance analyzer in 10kHz, 0.05V
In the case of test 0A inductance and plus 20A (i.e. 100Oe) DC stacked inductance, calculate and be superimposed percentage in 100Oe.Function
Rate loss is measured with Φ 0.5mm copper wire in such a way that 30 circles add 5 circles as a result, the μ of inductance L29.26~30.05 H, 200KhzQ value 61
~65, loss value of the power loss in 100kHz, 100mT is 450mW/cm3;It is superimposed performance 100Oe:61%;50Oe:80%.
Embodiment 3
75%Si Antaciron 10%, aluminum shot 6%, carbon dust 0.2 ‰, deslagging agent 0.5 ‰, surplus are taken based on mass fraction 100%
For 99.9% pure iron, aerosolization iron sial is prepared by smelting technology, selects 6.0 to let slip a remark, atomizing pressure 3.0Mpa prepares powder and goes out
Powder rate 77%;
It takes 200 mesh iron aluminum silicon powder 1kg to controllable temperature agitated kettle, 30% phosphate aqueous solution 100ml is added, phosphoric acid additive amount accounts for iron silicon
Aluminium powder weight ratio 2%, after uninterrupted stirring 2 hours, stirring pot temperature rises to 130 DEG C, roasts to drying, is put into powder after sieving
800 DEG C of annealing furnace 2 hours of annealing of nitrogen protection, potassium water glass 25g and silicon dioxide gel 25g are added, continues to stir,
Until dry.30g zinc stearate powdered lubricant is added, stirs evenly, by powder with 20 tons/cm3Pressure be pressed into OD27.0,
The standard magnet ring of ID14.8, HT11.0, are made annealing treatment under 750 ± 5 DEG C of nitrogen protections, Control for Oxygen Content when annealing
In 20ppm, heat treatment time is 180 minutes, is finally sprayed with epoxy resin coating.
Copper wire uses Φ 0.5mm, and 20 circle of coil turn is tested with HP4284 inductance analyzer in 100kHz, 1V
Inductance L and quality factor Q.Copper wire uses Φ 0.8mm, 25 circle of coil turn, with HP4284 inductance analyzer in 10kHz, 0.05V
In the case of test 0A inductance and plus 20A (i.e. 100Oe) DC stacked inductance, calculate and be superimposed percentage in 100Oe.Function
Rate loss is measured with Φ 0.5mm copper wire in such a way that 30 circles add 5 circles as a result, the μ of inductance L29.26~30.05 H, 200KhzQ value 61
~65, power loss is 500mW/cm3 in the loss value of 100kHz, 100mT;It is superimposed performance 100Oe:63%;50Oe:83%.
Table 1, powder physical chemistry test result
Claims (7)
1. a kind of technique for preparing iron sial powder using non-real air atomizing and making magnetic core, which is characterized in that the technique
The following steps are included:
1) major ingredient pure iron is taken, ferrosilicon, aluminum shot, auxiliary material is deslagging agent, carbon dust;
2) pure iron is put into intermediate frequency furnace, heated, soon melted completion to pure iron and be put into ferrosilicon, reduce frequency first after mixing evenly
Secondary fishing slag;
3) protective atmosphere gas curtain is opened after fishing out slag, pours into aluminum shot, quickly stirs and start thermometric, prepares atomization;
4) control of tundish initial temperature pours into molten steel and starts to be atomized at 1400 DEG C or more, keeps atomizing pressure;
5) it adjusts intermediate frequency furnace and Tundish Heating is kept for 1700 DEG C of molten steel temperature >, molten steel exposed part is formed during atomization and is protected
Protect atmosphere;
6) sub-sieve is carried out to original powder after the completion of being atomized, rod milling and airflow milling are sold, after selling rod milling again after nitrogen protection high annealing
It is stand-by to carry out mixing;
7) it takes powder to carry out carrying out physical chemistry detection, the phosphoric acid solution being diluted with water is added;
8) iron aluminum silicon powder reacts in phosphoric acid solution, and the reaction time is 1-2 hours, after the reaction was completed in 80 DEG C~130 DEG C situations
Under be dried;
9) iron aluminum silicon powder is annealed 1-2 hours in n 2 annealing furnace high temperature again after phosphorating treatment, and temperature is higher than 500 DEG C;
10) high temperature resistant binder waterglass, potassium water glass, composite phosphate, SiO2 colloidal sol are added after the completion of the insulation of iron aluminum silicon powder
One or more of, additive amount is 0.5~2%;
11) zinc stearate is added after the completion of iron aluminum silicon powder insulation adhesive as lubricant, is mixed magnetic powder and is pressed into iron sial core magnetic
Core;
12) ferrocart core magnetic core is in N2Annealing heat-treatment is carried out under atmosphere;
13) magnetic core spray epoxy paint;
14) 500~450mW/cm is lost in the 026 sendust core 100K/100mT of μ to the preparation of top method3;It is superimposed performance
100Oe:61~63%;50Oe:80~83%.
2. a kind of technique for preparing iron sial powder using non-real air atomizing and make magnetic core according to claim 1,
It is characterized in that, the mass fraction of each raw material is respectively as follows: major ingredient pure iron 80%~82% in step 1), ferrosilicon 9.5%~10%,
Aluminum shot 5%~6%, auxiliary material are deslagging agent 0.2 ‰, and carbon dust 0.5 ‰, surplus is inevitable impurity.
3. a kind of technique for preparing iron sial powder using non-real air atomizing and make magnetic core according to claim 1,
It is characterized in that, the temperature of thermometric reaches 1750 DEG C~1800 DEG C in step 3), start to be atomized.
4. a kind of technique for preparing iron sial powder using non-real air atomizing and make magnetic core according to claim 1,
It is characterized in that, keeping atomizing pressure in step 4) is 3.0Mpa.
5. a kind of technique for preparing iron sial powder using non-real air atomizing and make magnetic core according to claim 1,
It is characterized in that, the additive amount of lubricant is the 0.2-0.5% of iron aluminum silicon powder in step 11), the pressure of compacting is 20T/cm3。
6. a kind of technique for preparing iron sial powder using non-real air atomizing and make magnetic core according to claim 1,
It is characterized in that, the temperature being heat-treated in step 12) is 600-750 DEG C, Control for Oxygen Content is in 50ppm or less when annealing.
7. a kind of technique for preparing iron sial powder using non-real air atomizing and make magnetic core according to claim 1,
It is characterized in that, in step 13) epoxy resin coating with a thickness of 0.3-0.5mm.
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CN112071547A (en) * | 2020-09-16 | 2020-12-11 | 湖南特种金属材料有限责任公司 | Fe-Si-Al soft magnetic powder and preparation method thereof |
CN113035541A (en) * | 2021-02-03 | 2021-06-25 | 惠州市安可远磁性器件有限公司 | Method for coating iron-silicon powder with modified silica sol and method for manufacturing iron-silicon magnetic powder core |
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Application publication date: 20190115 Assignee: Jinhua cimeng Intellectual Property Service Co.,Ltd. Assignor: HENGDIAN GROUP DMEGC MAGNETICS Co.,Ltd. Contract record no.: X2023330000883 Denomination of invention: A process for preparing iron silicon aluminum powder and making magnetic cores using non vacuum atomization Granted publication date: 20200605 License type: Common License Record date: 20231128 |