CN102471162B - 铁氧体磁性材料 - Google Patents
铁氧体磁性材料 Download PDFInfo
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- CN102471162B CN102471162B CN201080030766.4A CN201080030766A CN102471162B CN 102471162 B CN102471162 B CN 102471162B CN 201080030766 A CN201080030766 A CN 201080030766A CN 102471162 B CN102471162 B CN 102471162B
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- magnetic material
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- 229910000859 α-Fe Inorganic materials 0.000 title claims abstract description 169
- 239000000696 magnetic material Substances 0.000 title claims abstract description 101
- 239000000203 mixture Substances 0.000 claims abstract description 43
- 239000013078 crystal Substances 0.000 claims abstract description 11
- 229910052748 manganese Inorganic materials 0.000 claims abstract description 7
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 7
- 229910052725 zinc Inorganic materials 0.000 claims abstract description 7
- 229910052802 copper Inorganic materials 0.000 claims abstract description 6
- 229910052749 magnesium Inorganic materials 0.000 claims abstract description 6
- 229910052761 rare earth metal Inorganic materials 0.000 claims abstract description 6
- 239000004615 ingredient Substances 0.000 claims description 16
- 229910052742 iron Inorganic materials 0.000 claims description 11
- 229910052788 barium Inorganic materials 0.000 claims description 8
- 229910052712 strontium Inorganic materials 0.000 claims description 8
- 229910052797 bismuth Inorganic materials 0.000 claims description 3
- 229910000828 alnico Inorganic materials 0.000 abstract description 17
- 229910052727 yttrium Inorganic materials 0.000 abstract description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 31
- 238000000034 method Methods 0.000 description 31
- 238000004519 manufacturing process Methods 0.000 description 25
- 239000000463 material Substances 0.000 description 25
- 239000002994 raw material Substances 0.000 description 23
- 239000011575 calcium Substances 0.000 description 19
- 230000008569 process Effects 0.000 description 19
- 238000010298 pulverizing process Methods 0.000 description 16
- 230000005389 magnetism Effects 0.000 description 13
- 239000002002 slurry Substances 0.000 description 12
- 238000010304 firing Methods 0.000 description 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- VTYYLEPIZMXCLO-UHFFFAOYSA-L calcium carbonate Substances [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 9
- 239000002245 particle Substances 0.000 description 9
- 239000000843 powder Substances 0.000 description 9
- 238000013329 compounding Methods 0.000 description 8
- 239000012298 atmosphere Substances 0.000 description 6
- 230000008859 change Effects 0.000 description 6
- 238000011156 evaluation Methods 0.000 description 6
- 230000005308 ferrimagnetism Effects 0.000 description 6
- 150000005846 sugar alcohols Polymers 0.000 description 6
- 230000033228 biological regulation Effects 0.000 description 5
- 229910000019 calcium carbonate Inorganic materials 0.000 description 5
- 239000011572 manganese Substances 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 5
- 238000005245 sintering Methods 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000011701 zinc Substances 0.000 description 5
- AYJRCSIUFZENHW-UHFFFAOYSA-L barium carbonate Chemical compound [Ba+2].[O-]C([O-])=O AYJRCSIUFZENHW-UHFFFAOYSA-L 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 230000008602 contraction Effects 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- 239000006185 dispersion Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000011777 magnesium Substances 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 229910052681 coesite Inorganic materials 0.000 description 3
- 229910052906 cristobalite Inorganic materials 0.000 description 3
- 229910052746 lanthanum Inorganic materials 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- 229910052682 stishovite Inorganic materials 0.000 description 3
- 229910052905 tridymite Inorganic materials 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 238000005303 weighing Methods 0.000 description 3
- 238000001238 wet grinding Methods 0.000 description 3
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 2
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- 229920000459 Nitrile rubber Polymers 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- UBEWDCMIDFGDOO-UHFFFAOYSA-N cobalt(II,III) oxide Inorganic materials [O-2].[O-2].[O-2].[O-2].[Co+2].[Co+3].[Co+3] UBEWDCMIDFGDOO-UHFFFAOYSA-N 0.000 description 2
- 238000012790 confirmation Methods 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical compound [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 description 2
- BDAGIHXWWSANSR-NJFSPNSNSA-N hydroxyformaldehyde Chemical compound O[14CH]=O BDAGIHXWWSANSR-NJFSPNSNSA-N 0.000 description 2
- 229910052738 indium Inorganic materials 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 230000005415 magnetization Effects 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 239000011164 primary particle Substances 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 238000007493 shaping process Methods 0.000 description 2
- 229910000018 strontium carbonate Inorganic materials 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- JRIGVWDKYXCHMG-UHFFFAOYSA-N (5-arsoroso-2-hydroxyphenyl)azanium;chloride Chemical compound Cl.NC1=CC([As]=O)=CC=C1O JRIGVWDKYXCHMG-UHFFFAOYSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 238000004438 BET method Methods 0.000 description 1
- RGHNJXZEOKUKBD-SQOUGZDYSA-M D-gluconate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O RGHNJXZEOKUKBD-SQOUGZDYSA-M 0.000 description 1
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 1
- 229910020854 La(OH)3 Inorganic materials 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- XHCLAFWTIXFWPH-UHFFFAOYSA-N [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] XHCLAFWTIXFWPH-UHFFFAOYSA-N 0.000 description 1
- IKWTVSLWAPBBKU-UHFFFAOYSA-N a1010_sial Chemical compound O=[As]O[As]=O IKWTVSLWAPBBKU-UHFFFAOYSA-N 0.000 description 1
- 230000004523 agglutinating effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- 229910000413 arsenic oxide Inorganic materials 0.000 description 1
- 229960002594 arsenic trioxide Drugs 0.000 description 1
- 229910052790 beryllium Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- QDOXWKRWXJOMAK-UHFFFAOYSA-N chromium(III) oxide Inorganic materials O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 description 1
- 229960004643 cupric oxide Drugs 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- AJNVQOSZGJRYEI-UHFFFAOYSA-N digallium;oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[Ga+3].[Ga+3] AJNVQOSZGJRYEI-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 229910001195 gallium oxide Inorganic materials 0.000 description 1
- 229910052732 germanium Inorganic materials 0.000 description 1
- YBMRDBCBODYGJE-UHFFFAOYSA-N germanium oxide Inorganic materials O=[Ge]=O YBMRDBCBODYGJE-UHFFFAOYSA-N 0.000 description 1
- 229940050410 gluconate Drugs 0.000 description 1
- 239000000174 gluconic acid Substances 0.000 description 1
- 235000012208 gluconic acid Nutrition 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 229910003437 indium oxide Inorganic materials 0.000 description 1
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- CMGJQFHWVMDJKK-UHFFFAOYSA-N lanthanum;trihydrate Chemical compound O.O.O.[La] CMGJQFHWVMDJKK-UHFFFAOYSA-N 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- 229940074869 marquis Drugs 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 229910000476 molybdenum oxide Inorganic materials 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910000480 nickel oxide Inorganic materials 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 239000010955 niobium Substances 0.000 description 1
- 229910000484 niobium oxide Inorganic materials 0.000 description 1
- URLJKFSTXLNXLG-UHFFFAOYSA-N niobium(5+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Nb+5].[Nb+5] URLJKFSTXLNXLG-UHFFFAOYSA-N 0.000 description 1
- QGLKJKCYBOYXKC-UHFFFAOYSA-N nonaoxidotritungsten Chemical compound O=[W]1(=O)O[W](=O)(=O)O[W](=O)(=O)O1 QGLKJKCYBOYXKC-UHFFFAOYSA-N 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- PVADDRMAFCOOPC-UHFFFAOYSA-N oxogermanium Chemical compound [Ge]=O PVADDRMAFCOOPC-UHFFFAOYSA-N 0.000 description 1
- PQQKPALAQIIWST-UHFFFAOYSA-N oxomolybdenum Chemical compound [Mo]=O PQQKPALAQIIWST-UHFFFAOYSA-N 0.000 description 1
- GNRSAWUEBMWBQH-UHFFFAOYSA-N oxonickel Chemical compound [Ni]=O GNRSAWUEBMWBQH-UHFFFAOYSA-N 0.000 description 1
- 229950008475 oxophenarsine Drugs 0.000 description 1
- BPUBBGLMJRNUCC-UHFFFAOYSA-N oxygen(2-);tantalum(5+) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Ta+5].[Ta+5] BPUBBGLMJRNUCC-UHFFFAOYSA-N 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- VBUNOIXRZNJNAD-UHFFFAOYSA-N ponazuril Chemical compound CC1=CC(N2C(N(C)C(=O)NC2=O)=O)=CC=C1OC1=CC=C(S(=O)(=O)C(F)(F)F)C=C1 VBUNOIXRZNJNAD-UHFFFAOYSA-N 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000004445 quantitative analysis Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 229910052701 rubidium Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- 229910001936 tantalum oxide Inorganic materials 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 229910001930 tungsten oxide Inorganic materials 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 229910001935 vanadium oxide Inorganic materials 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
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- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
- C04B35/46—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on titanium oxides or titanates
- C04B35/462—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on titanium oxides or titanates based on titanates
- C04B35/465—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on titanium oxides or titanates based on titanates based on alkaline earth metal titanates
- C04B35/468—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on titanium oxides or titanates based on titanates based on alkaline earth metal titanates based on barium titanates
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
- C04B35/26—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on ferrites
- C04B35/2608—Compositions containing one or more ferrites of the group comprising manganese, zinc, nickel, copper or cobalt and one or more ferrites of the group comprising rare earth metals, alkali metals, alkaline earth metals or lead
- C04B35/2633—Compositions containing one or more ferrites of the group comprising manganese, zinc, nickel, copper or cobalt and one or more ferrites of the group comprising rare earth metals, alkali metals, alkaline earth metals or lead containing barium, strontium or calcium
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G49/00—Compounds of iron
- C01G49/0018—Mixed oxides or hydroxides
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G49/00—Compounds of iron
- C01G49/0018—Mixed oxides or hydroxides
- C01G49/0036—Mixed oxides or hydroxides containing one alkaline earth metal, magnesium or lead
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
- C01G49/00—Compounds of iron
- C01G49/009—Compounds containing, besides iron, two or more other elements, with the exception of oxygen or hydrogen
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
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- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
- C04B35/26—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on ferrites
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- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
- C04B35/26—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on ferrites
- C04B35/2641—Compositions containing one or more ferrites of the group comprising rare earth metals and one or more ferrites of the group comprising alkali metals, alkaline earth metals or lead
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- C—CHEMISTRY; METALLURGY
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- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/626—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
- C04B35/62605—Treating the starting powders individually or as mixtures
- C04B35/6261—Milling
- C04B35/6262—Milling of calcined, sintered clinker or ceramics
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- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/626—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
- C04B35/63—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B using additives specially adapted for forming the products, e.g.. binder binders
- C04B35/632—Organic additives
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Abstract
本发明是以提供一种能够获得维持高Br以及高HcJ而且具有高Hk/HcJ的永久性磁铁的铁氧体磁性材料为目的的。优选的实施方式所涉及的铁氧体磁性材料具备拥有六方晶结构的铁氧体相,并具有由Ca1-w-x-yRwSrxBayFezMmO19[式中,R是选自稀土类元素(包含Y)以及Bi中的至少1种元素,且必须包含La,M是选自Co、Mn、Mg、Ni、Cu以及Zn中的至少1种元素,且必须包含Co]所表示的主要组成,满足以下所述关系式0.25<w<0.65,0.01<x<0.45,0.0002<y<0.011,y<x,8<z<11,1.0<w/m<2.5,0.017<m/z<0.065,Si成分的总量相对于主要组成为0.1~3质量%,而且各个元素满足1.5≤[(Ca+R+Sr+Ba)-(Fe+M)/12]/Si≤3.5的关系。
Description
技术领域
本发明涉及铁氧体磁性材料。
背景技术
作为由氧化物构成的永久性磁铁的材料,众所周知有六方晶类的M型(磁铁铅矿型)Sr铁氧体或者Ba铁氧体。由这些铁氧体构成的铁氧体磁性材料是以铁氧体烧结体和粘结磁铁的形式作为永久性磁铁被加以提供的。近年来,伴随着电子零部件的小型化以及高性能化而即使相对于由铁氧体磁性材料构成的永久性磁铁也不断要求既要是小型的又要具有高磁气特性。
作为永久性磁铁的磁气特性的指标一般是使用剩余磁通量密度(Br)以及矫顽(磁)力(HcJ)来评价这些指标为高的具有高磁气特性。一直以来,从提高永久性磁铁的Br以及HcJ的观点出发,以在铁氧体磁性材料中含有规定的元素的方法等以及经改变其组成来加以研究探讨。
例如,在以下所述专利文献1中介绍了通过在M型Ca铁氧体中至少含有La、Ba以及Co从而获得具有高Br以及高HcJ的铁氧体烧结磁铁的氧化物磁性材料。
另外,在以下所述专利文献2中介绍了通过使M型Ca铁氧体中含有La、Sr以及Co从而获得具有高Br以及高HcJ的铁氧体烧结磁铁的氧化物磁性材料。而且,在以下所述专利文献3中公开了通过在M型Sr铁氧体中含有Sr、La以及Co从而具有高Br以及高HcJ的烧结磁铁。
专利文献
专利文献1:日本专利第4078566号公报
专利文献2:国际公开2007/077811号小册子
专利文献3:日本专利第3163279号公报
发明内容
发明所要解决的课题
如以上所述,为了良好地获得Br以及HcJ这两个数据而尝试了种种改变添加到主要组成的元素的组合,但是到底怎样的添加元素的组合才能够给出高特性,这至今仍然还未明了。
另外,在永久性磁铁中除了具有高Br以及高HcJ之外,优选磁化为Br的90%时的磁场的值(Hk)相对于HcJ的比率即所谓矩形比(squarenessratio)(Hk/HcJ)也要高。如果Hk/HcJ高的话那么由于外部磁场和温度变化而引起的减磁就小,且变得能够获得稳定的磁气特性。
因此,关于使用了铁氧体磁性材料的永久性磁铁,优选在获得高Br以及高HcJ的同时能够获得表现优异的Hk/HcJ。然而,如果提高了任意一个特性的话那么其它特性发生下降等,要制得能够获得具有像这样3个特性的永久性磁铁的铁氧体磁性材料一直以来绝不是件容易的事。
因此,本发明就是借鉴了以上所述那样的情况而做出的不懈努力之结果,是以提供一种能够获得维持高Br以及高HcJ而且具有高Hk/HcJ的永久性磁铁的铁氧体磁性材料以及由这样的铁氧体磁性材料构成的磁铁为目的的。
解决课题的手段
为了达到以上所述目的,本发明的铁氧体磁性材料,其特征为:是一种具备由铁氧体相构成的主相的铁氧体磁性材料,所述铁氧体磁性材料具有六方晶结构;具有由以下所述式(1)所表示的主要组成:
Ca1-w-x-yRwSrxBayFezMmO19(1)
[式1中,R是选自稀土类元素(包含Y)以及Bi中的至少1种元素且至少含有La,M是选自Co、Mn、Mg、Ni、Cu以及Zn中的至少1种元素且至少含有Co]
在式(1)中w、x、y、z以及m满足以下所述式(2)、(3)、(4)、(5)、(6)、(7)以及(8),
0.25<w<0.65(2)
0.01<x<0.45(3)
0.0002<y<0.011(4)
y<x(5)
8<z<11(6)
1.0<w/m<2.5(7)
0.017<m/z<0.065(8)
作为副成分至少含有Si成分,该Si成分的总量相对于主要组成为0.1~3质量%,而且Ca、R、Sr、Ba、Fe、M以及Si的摩尔比满足以下所述式(9)。
1.5≤[(Ca+R+Sr+Ba)-(Fe+M)/12]/Si≤3.5(9)
上述本发明的铁氧体磁性材料在由以上所述式(1)加以表示并且各元素满足式(2)~(8)的条件的同时,作为副成分而进一步含有Si成分,并且进一步通过构成主要组成的金属元素和Si满足式(9)所表示的关系,从而变成一种不仅具有高Br以及高HcJ而且还具有高Hk/HcJ的铁氧体磁性材料。
另外,本发明提供了一种以下所述的磁铁,即,由上述本发明的铁氧体磁性材料所构成并具有弧段形状而且该形状的中心角为30°以上,优选为60°以上。
像这样的弧段形状的铁氧体永久性磁铁在马达等领域中有着广泛的运用,根据上述本发明的铁氧体磁性材料,就能够提供一种具有高Br、高HcJ以及高Hk/HcJ的弧段形状的磁铁。
另外,本发明的铁氧体磁性材料对于形成具有像这样形状的磁铁来说是极为有利的。即,由铁氧体磁性材料构成弧段形状的磁铁多数是由铁氧体磁性材料的烧结体所构成。像这样的磁铁是通过以下所述方式来加以制造的,即,使用烧结前的铁氧体磁性材料来形成成形体并烧成这个成形体。在要获得弧段形状的烧结体的情况下使用对应于此的形状的成形体。
成形体通常在烧成时是以一定的比例进行收缩的,在磁场被定向的情况下如果以结晶组织来看的话,那么收缩率在c轴(磁化容易轴)方向和a轴方向上有着较大的差异,通常c轴方向的收缩率较a轴方向的收缩率来得大。为此,在制成弧段形状并将结晶组织定向成圆弧状来加以排列的情况下,由这个收缩率之差(缩率比)能够表示在烧成时中心角发生进一步变大那样的收缩举动。为此,为了获得具有所希望的中心角的各向异性的形状,成形体鉴于像这样的收缩举动而预先放浅圆弧(缩小中心角)。尽管如此,在制造圆弧深的形状的磁铁的情况下,在成形体的阶段,将圆弧加深到某一程度以上仍然是有必要的。
在打算要取得中心角成为30°以上那样的磁铁的情况下,因为成形体的圆弧也被控制得相当深,所以例如在成形时不让两端附近充分凝固,因而对于成形来说有必要需要较长的时间,或者有必要加大成形压力,与以往的技术相比较相对要求更严的成形条件。其结果除了生产性变低之外,会有所获得的磁铁的特性也容易发生降低的倾向。为此,一直以来,制造具有中心角成为30°以上那样的各向异性的铁氧体烧结磁铁是困难的。
相对于此,本发明的铁氧体磁性材料因为具有以上所述那样的特定组成,所以能够发挥出所谓增大成形体烧成时的缩率比的效果。为此,根据该铁氧体磁性材料,与以往技术相比较能够在烧成时利用大缩率比来容易地从圆弧浅的成形体制得圆弧深的(中心角大)烧结体。因此,由本发明的铁氧体磁性材料构成弧段形状的磁铁就能够容易得拥有所谓30°以上优选为60°以上的大中心角。
发明效果
根据本发明,可提供一种能够获得维持高Br以及高HcJ而且不仅具有高Hk/HcJ并具有大中心角的弧段形状的永久性磁铁的铁氧体磁性材料。
附图说明
图1是表示优选的实施方式的铁氧体永久性磁铁的立体图。
图2是分别表示磁铁1的平面以及端面的图。
符号说明
1.磁铁
具体实施方式
以下是一边参照附图一边就有关本发明的优选的实施方式加以说明。在图面的说明中将相同的符号标注于相同的要素,从而避免重复说明。
(铁氧体永久性磁铁)
图1是表示优选的实施方式的铁氧体永久性磁铁的立体图。图1所表示的铁氧体永久性磁铁1(以下仅称之为“磁铁1”)具有以其端面成为圆弧状的形式进行弯曲的形状,一般具有被称之为弧段形状、C字形状、瓦片形状、弓形状等的形状。该磁铁1是由铁氧体磁性材料的烧结体所构成,是一种铁氧体烧结磁铁。
构成磁铁1的铁氧体磁性材料是一种具备由拥有六方晶结构的铁氧体相构成的主相的铁氧体磁性材料,优选为磁铁铅矿型(M型)铁氧体。在此。所谓主相是指在构成铁氧体烧结体的结晶粒子和在形成于该粒子之间的晶界中构成结晶粒子的部分,在优选的情况下占烧结体的95体积%以上。
本实施方式的铁氧体磁性材料具有由以下所述式(1)所表示的主要组成。该主要组成包含于以上所述的主相中并且形成六方晶结构。
Ca1-w-x-yRwSrxBayFezMmO19(1)
在此,在式1中R是选自稀土类元素(包含Y)以及Bi中的至少1种元素且至少含有La,M是选自Co、Mn、Mg、Ni、Cu以及Zn中的至少1种元素且至少含有Co。
在式(1)中w、x、y、z以及m分别表示R、Sr、Ba、Fe以及M的原子比率,并满足所有以下所述式(2)、(3)、(4)、(5)、(6)、(7)以及(8),
0.25<w<0.65(2)
0.01<x<0.45(3)
0.0002<y<0.011(4)
y<x(5)
8<z<11(6)
1.0<w/m<2.5(7)
0.017<m/z<0.065(8)
另外,铁氧体磁性材料作为以上所述的主要组成以外的副成分至少含有Si成分,该Si成分的总量相对于主要组成为0.1~3质量%。所谓Si成分是在构成元素中含有Si的成分,在含有多种Si成分的情况下其合计量成为以上所述的“总量”。
而且,在铁氧体磁性材料中Ca、R、Sr、Ba、Fe、M以及Si各个元素其摩尔比成为满足以下所述式(9)的关系。
1.5≤[(Ca+R+Sr+Ba)-(Fe+M)/12]/Si≤3.5(9)
以下是就有关以上所述铁氧体磁性材料的组成作进一步详细的说明。
在上述主要组成中的Ca的原子比例(1-w-x-y)优选为超过0.05不到0.59。如果Ca的原子比例过小,那么就会有铁氧体磁性材料不能成为M型铁氧体的情况。另外,除了增加α-Fe2O3等非磁性相的比例之外,R成为剩余从而生成正铁氧体(orthoferrite)等非磁性的异相,并会有磁气特性(特别是Br和HcJ)发生下降的倾向。另外,如果Ca的原子比例过大,那么除了会有不能成为M型铁氧体的情况之外,CaFeO3-x等非磁性相变多从而会担忧磁气特性发生下降。
由R所表示的元素除了至少含有La之外,作为La之外的元素优选为选自稀土类元素(包含Y)以及Bi中的至少1种,更加优选为选自稀土类元素中的至少1种。但是,作为R从提高各向异性磁场的观点出发特别优选只含有La。
主要组成中的R的原子比率(w)为超过0.25不到065,如果在该范围内的话,那么就能够很好地获得理想的Br和HcJ以及Hk/HcJ。如果R的原子比率过小的话,那么铁氧体磁性材料中的M的固溶量将变得不够充分,并且Br以及HcJ降低。另外,如果过大的话,那么就会产生正铁氧体等非磁性的异相,且Hk/HcJ变低从而获得实用的磁铁将变困难。从如此的观点出发优选R的原子比率为0.3~0.55,更加优选为0.35~0.5。
Sr的原子比率(x)为超过0.01不到0.45,通过控制在该范围内从而良好的Br、HcJ以及Hk/HcJ被满足。如果Sr的原子比率为过小的话,那么Ca和/或La的比率则变大且Hk/HcJ降低。另外,如果Sr的原子比率过大的话,那么Br以及HcJ则变得不够充分。从如此的观出发Sr的原子比率优选为0.05~0.35,更加优选为0.05~0.2。
Ba的原子比率(y)为超过0.0002不到0.011,通过控制在该范围内从而良好的Br、HcJ以及Hk/HcJ被满足。如果Ba的原子比率为过小的话,那么就不能够得到充分提高Hk/HcJ的效果。另外,如果过大的话,那么Br以及HcJ则会不适合地发生下降。从如此的观点出发,Ba的原子比率优选为0.0006~0.010。
另外,Sr的原子比率(x)以及Ba的原子比率(y)满足y<x的关系。就这样通过使Sr的原子比率变成比Ba的原子比率来得大,从而除了获得良好的Br以及除了变得容易获得充分高的Hk/HcJ之外,增大后面所述那样的缩率比而变得容易获得弧段形状的磁铁。
Fe的原子比率(z)为超过8不到11,通过控制在该范围内从而良好的Br、HcJ以及Hk/HcJ被满足。Fe的原子比率过小过大都会使Br以及HcJ不合适地发生降低。Fe的原子比率优选为8.5~10.5,更加优选为9~10。
由M所表示的元素除了至少含有Co之外,作为Co之外的元素优选为选自Mn、Mg、Ni、Cu以及Zn中的至少1种,更加优选为选自Mn、Ni以及Zn中的至少1种。但是,作为M从提高各向异性磁场的观点出发特别优选只含有Co。
铁氧体磁性材料的主要组成关于M的原子比率(m)首先要满足m/z超过0.017不到0.065的条件。另外,要满足w/m超过1.0不到2.5的条件。通过满足这些条件从而就能够获得良好的Br、HcJ以及Hk/HcJ。在M的原子比率为过小的情况下,则不能够获得良好的Br以及HcJ,特别是如果Co的比率过小的话,那么就不能够获得良好的HcJ。另外,在M的比率为过大的情况下,会有Br以及HcJ发生降低的倾向。
从如此的观点出发m/z优选为0.02~0.05,更加优选为0.022~0.04。另外,w/m优选为1.2~2.0,更加优选为1.5~1.8。
铁氧体磁性材料除了以上所述的主要组成之外还包含后面所述的副成分。无论是在铁氧体磁性材料的主相以及晶界都可以包含副成分。在铁氧体磁性材料中除了整体中的副成分之外便是主要组成。从获得充分的磁气特性的观点出发,在铁氧体磁性材料中主要组成的含有比例优选为90质量%以上,更加优选为95~100质量%。
本实施方式的铁氧体磁性材料作为副成分至少含有Si成分。作为Si成分只要具有含有Si的组成,那么就没有特别的限定,例如也可以以SiO2、Na2SiO3、SiO2·nH2O等形态进行添加。铁氧体磁性材料通过含有Si成分从而烧结性将变得良好,另外,适度调整烧结体的结晶粒径就能够成为磁气特性良好地被控制的铁氧体磁性材料。其结果既能够良好地维持Br以及HcJ又能够获得高Hk/HcJ。
在铁氧体磁性材料中,Si成分的含量以所有的Si成分的合计量换算成SiO2为0.1~3质量%。Si成分如果是这样的含量的话那么就能够获得高HcJ。
另外,Ca、R、Sr、Ba、Fe、M以及Si的摩尔比满足以下所述式(9)。
1.5≤[(Ca+R+Sr+Ba)-(Fe+M)/12]/Si≤3.5(9)
在此,磁铁铅矿型构造一般是以AB12O19来表示的。在充当该组成的情况下以上所述式(9)中的[(Ca+R+Sr+Ba)-(Fe+M)/12]/Si能够被表示为(A-B/12)/Si。由此,该式是表示被认为从主相溢出从而存在于晶界的A位点(site)成分以及Si成分的晶界中的存在比(A位点成分/Si成分)。
本实施方式的铁氧体磁性材料通过满足以上所述式(9)的条件,从而即使是A位点元素为较多的(B位点元素为较少)那样的背离于化学计量比的组成,也变得好像能够良好地保持M型构造。其结果在维持高磁气特性(Br以及HcJ)的同时,能够获得优异的Hk/HcJ。从更好地获得像这样的效果的观点出发,[(Ca+R+Sr+Ba)-(Fe+M)/12]/Si优选为1.5~3.5,更加优选为1.5~3.0。
铁氧体磁性材料含有以上所述的主要组成以及至少包含Si成分的副成分,铁氧体磁性材料的组成可以由荧光X线定量分析来加以测定。另外,主相的存在可以由X线衍射或者电子线衍射来加以确认。
本实施方式的铁氧体磁性材料作为副成分也可以含有除了Si成分之外的成分。作为其它副成分例如可以有Al和/或Cr。由此,磁铁1的HcJ有着一种提高的倾向。从获得良好的HcJ的向上效果的观点出发,Al和/或Cr的含量相对于铁氧体磁性材料整体被换算成Al2O3或者Cr2O3而优选为0.1质量%以上。但是,这些成分因为会有使磁铁1的Br降低的情况,所以从获得良好的Br的观点出发优选为3质量%以下。
另外,作为副成分也可以将B作为例如B2O3而含有。通过含有B,从而就能够降低在制得由铁氧体磁性材料构成的烧结体的时候的预烧温度和烧结温度,并且变得能够生产性良好地制得磁铁1。但是,如果B的含量过多的话那么因为会有磁铁1的饱和磁化发生降低的情况,所以B的含量相对于铁氧体磁性材料整体作为B2O3而优选为0.5质量%以下。
而且,铁氧体磁性材料作为副成分可以以氧化物的形态含有Ga、Mg、Cu、Mn、Ni、Zn、In、Li、Ti、Zr、Ge、Sn、V、Nb、Ta、Sb、As、W、Mo等。这些元素的含量被换算成各个原子的化学计量组成的氧化物而优选为氧化镓5质量%以下,氧化镁5质量%以下,氧化铜5质量%以下,氧化锰5质量%以下,氧化镍5质量%以下,氧化锌5质量%以下,氧化铟3质量%以下,氧化锂1质量%以下,氧化钛3质量%以下,氧化锆3质量%以下,氧化锗3质量%以下,氧化锡3质量%以下,氧化钒3质量%以下,氧化铌3质量%以下,氧化钽3质量%以下,氧化锑3质量%以下,氧化砷3质量%以下,氧化钨3质量%以下,氧化钼3质量%以下。但是,在多种类组合这些物质来加以含有的情况下为了避免磁气特性的降低而优选其合计含量成为5质量%以下。
还有,铁氧体磁性材料中,作为副成分优选不含有碱金属元素(Na、K、Rb等)。碱金属元素的存在会有使磁铁1的饱和磁化降低的倾向。但是,也会有碱金属元素例如被包含于为了制得铁氧体磁性材料的原料中的情况,如果是像这样含有不可避免的程度的话,那么在铁氧体磁性材料中含有也并非不可。不对磁气特性产生大影响的碱金属元素的含量为3质量%以下。
构成磁铁1的铁氧体磁性材料正如以上所述其形态为烧结体,并且具有包含结晶粒子(主相)和晶界的构造。该烧结体中的结晶粒子的平均结晶粒径优选为1.5μm以下,更优选为1.0μm以下,进一步优选为0.5~1.0μm。通过拥有像这样的平均结晶粒径,从而就变得容易获得高HcJ。铁氧体磁性材料的烧结体的结晶粒径可以由扫描型电子显微镜来加以测定。
磁铁1如以上所述是一种以端面成为圆弧状的形式使平板状的磁铁在一个方向上进行弯曲的具有弧段形状的磁铁。图2是从上方看到该磁铁1的平面图以及从侧面看到的端面图。如以上所述,磁铁1具备拥有规定中心角的扇形的平面形状。在此,所谓弧段形状的磁铁的中心角是以以下所述形式进行定义的值。即,所谓中心角是将在具有圆弧状的端面上的外侧边设想成圆弧的时候的该圆弧的中心角,在图2所表示的端面图中是以θ来表示的。具有像这样形状的磁铁1在图2的端面图中一般是以在用OR来表示的箭头方向上具有径向各向异性的形式对结晶组织进行配向。
在此,本实施方式的磁铁1因为是由具有以上所述的组成以及结晶组织的铁氧体磁性材料的烧结体所构成,所以在具有像这样的弧段形状的情况下,在烧成成形体而获得烧结体的时候,由a轴方向与c轴方向的收缩率之差通常显示出由于烧成而使中心角变得更大那样的收缩举动。还有,该收缩率之差例如可以由缩率比(c轴方向的收缩率/a轴方向的收缩率)来表示,该缩率比基本上是由铁氧体磁性材料的组成来决定的。缩率比越大,越是在制作成为弧段形状的情况下在圆弧的切线方向与圆弧的法线方向的收缩程度上产生差值,作为整体而变得会产生中心角变大那样的收缩。
于是,根据能够产生像这样高的缩率比的本实施方式的铁氧体磁性材料,能够容易地从圆弧浅的成形体利用烧成时的大缩率比来制得圆弧深的(中心角大)烧结体。因此,由本实施方式的铁氧体磁性材料对于制得具有所谓30°以上优选为60°以上的大中心角的磁铁1来说是有利的。
以上虽就有关优选的实施方式所涉及的磁铁1作了说明,但是由本发明而获得的磁铁只要是由本发明的铁氧体磁性材料构成的磁铁,并不限定于以上所述的形态。例如,磁铁除了具有各向异性的弧段形状之外,还可以具有平板状以及圆柱状等种种形状。即使是除了弧段形状之外的形状,只要是由本发明的铁氧体磁性材料所构成的,那么既能够维持高Br以及HcJ又能够获得高Hk/HcJ。
另外,磁铁1并不限定于由以上所述那样的铁氧体磁性材料的烧结体构成的磁铁,例如也可以是由胶粘剂来结合铁氧体磁性材料的粉末而形成的粘结磁铁。
在此情况下,以上所述那样的铁氧体磁性材料的条件,如果是满足于铁氧体磁性材料的粉末即可。构成铁氧体磁性材料的粉末的一次粒子的平均粒径虽然没有特别的限制,但是优选为2μm以下,更优选为1μm以下,进一步优选为0.1~1μm。如果该平均粒径为过大的话,那么粉末中的多磁区粒子的比率则变高,并且要担心HcJ会降低。另外,如果平均粒径过小的话,那么会由于热扰乱而降低磁性,或者在磁场中进行形成的时候的定向性和成形性变差。
作为胶粘剂可以列举丁腈橡胶(例如NBR橡胶)、聚氯乙烯、聚酰胺树脂[例如尼龙6、尼龙12(注册商标)]等。
(铁氧体永久性磁铁的制造方法)
接着,就有关以上所述那样的铁氧体永久性磁铁的制造方法的优选实施方式作如下说明。在以下的实施方式中,将展示一个由铁氧体磁性材料构成的铁氧体烧结磁铁的制造方法的例子。在本实施方式中,铁氧体烧结磁铁能够经过配合工序、预烧工序、粉碎工序、成形工序以及烧成工序来加以制造。关于各个工序将在以下作逐一说明。
<配合工序>
在配合工序中是配合铁氧体磁性材料的原料来获得原料组合物。首先,作为铁氧体磁性材料的原料可以列举含有构成铁氧体磁性材料的元素中1种或者2种以上的化合物(原料化合物)。原料化合物例如优选粉末状的物质。作为原料化合物可以列举各个元素的氧化物或者由烧成而成为氧化物的化合物(碳酸盐、氢氧化物、硝酸盐等)。例如可以例示SrCO3、La(OH)3、Fe2O3、BaCO3、CaCO3以及Co3O4等。原料化合物的粉末的平均粒径例如从能够均质配合的观点出发优选为0.1~2.0μm的程度。
另外,作为铁氧体磁性材料中的Si成分的原料可以列举SiO2,如果是含有Si的化合物等则没有特别的限制。另外,也可以在原料粉末中对应于必要配合一些其它副成分的原料化合物(元素单质、氧化物等)。
配合例如可以通过以获得所希望的铁氧体磁性材料的组成的形式对各个原料实施称量,在进行混合后使用湿式磨碎机、球磨机等并对原料进行0.1~20小时左右的混合以及粉碎处理来加以实行。
还有,在这个配合工序中没有必要混合所有的原料,其中一部分可以在后面所述的预烧之后进行添加。例如,副成分Si的原料(例如SiO2)和主要组成的构成元素Ca的原料(例如CaCO3)也可以在后面所述的预烧之后在粉碎(特别是微分碎)工序中进行添加。添加的时机只要是以容易获得所希望的组成和磁气特性的形式加以调整的话即可。
<预烧工序>
在预烧工序中是预烧在配合工序中所获得的原料粉末。预烧例如优选在空气中等氧化性气氛中进行。预烧温度优选为1100~1400℃的温度范围,更优选为1100~1300℃,进一步优选为1100~1250℃。预烧时间可以是1秒钟~10小时,优选为1秒钟~3小时。由预烧而获得的预烧体含有70%以上的上述那样的主相(M相)。主相的一次粒子径优选为10μm以下,更加优选为2μm以下。
<粉碎工序>
在粉碎工序中粉碎由预烧工序形成的颗粒状和块状的预烧体,并再一次粉碎成粉末状。由此,后面所述的成形工序中的成形就变得容易了。在这个粉碎工序中可以添加在以上所述那样的配合工序中没有配合的原料(原料的后添加)。粉碎工序例如在以成为粗粉末的形式粉碎预烧体(粗粉碎),之后再进一步对粗粉末作细微粉碎(微粉碎),即可以以两个阶段的工序来实行粉碎。
粗粉碎例如可以用振动研磨机等直至平均粒径成为0.5~5.0μm为止进行粉碎。关于微粉碎是进一步由湿式磨碎机、球磨机以及喷射研磨机等来粉碎在粗粉碎工序中所获得的粗粉碎材料。在微粉碎过程中是以所获得的微粉碎材料的平均粒径优选为0.08~2.0μm;更优选为0.1~1.0μm;进一步优选为0.2~0.8μm的形式实行粉碎的。微粉碎材料的比表面积(例如由BET法加以求得)优选为7~12m2/g左右。优选的粉碎时间根据粉碎方法而有所不同,例如在湿式磨碎机的情况下优选30分钟~10小时,由球磨机进行的湿式粉碎则优选为10~50小时左右。
在粉碎工序中添加原料的一部分的情况下,例如添加能够在微粉碎过程中加以实施。在本实施方式中虽然能够在微粉碎的时候添加作为Si成分的SiO2和作为Ca成分的CaCO3,但是也能够在配合工序和粗粉碎工序中添加这些化合物。
另外,在微粉碎工序中,为了提高在烧成后所获得的烧结体的磁气(性)的定向度而优选添加例如以一般式Cn(OH)nHn+2表示的多元醇。在此,作为多元醇在一般式中n优选为4~100的数,更优选为4~30的数,进一步优选为4~20的数,最优选为4~12的数。作为多元醇例如可以列举山梨醇。另外,也可以合并使用2个种类以上的多元醇。此外,除了多元醇之外也可以合并使用其它公知的分散剂。
在添加多元醇的情况下,其添加量相对于添加对象(例如粗粉碎材料)优选为0.05~5.0质量%,更优选为0.1~3.0质量%,进一步优选为0.2~2.0质量%。此外,在微粉碎工序中进行添加的多元醇在后面所述的烧成工序中被热分解去除。
<成形工序>
在成形工序中,在磁场中对在粉碎工序后所获得的粉碎材料(优选为微分碎材料)进行成形从而制得成形体。成形体可以以干式成形以及湿式成形的任一个方法来加以实行。从提高磁气(性)的定向度的观点出发优选以湿式成形来加以实行。
在由湿式成形来加以成形的情况下,例如优选在通过以湿式来实行以上所述的微粉碎工序从而获得浆料之后,将该浆料浓缩到规定的浓度并制得湿式成形用浆料,使用该浆料来实施成形。浆料的浓缩可以由离心分离和压滤等来加以实行。湿式成形用浆料优选为在其全量中微粉碎材料占30~80质量%的程度。在浆料中作为分散微粉碎材料的分散溶剂优选为水。在此情况下,在浆料中也可以添加葡萄糖酸、葡萄糖酸盐以及山梨醇等表面活性剂。另外,作为分散溶剂也可以使用非水类溶剂。作为非水类溶剂可以使用甲苯和二甲苯等有机溶剂。在此情况下,优选添加油酸等表面活性剂。此外,湿式成形用浆料也可以通过将分散溶剂等添加到微粉碎后的干燥状态的微粉碎材料中来加以调制。
关于湿式成形,接着相对于该湿式成形用浆料来实行磁场中成形。在此情况下,成行压力优选为9.8~49MPa(0.1~0.5ton/cm2)左右,所施加的磁场优选为398~1194kA/m(5~15kOe)左右。
在本实施方式中,因为是形成由本发明的铁氧体磁性材料构成的磁铁1,所以在如以上所述那样制造弧段形状的磁铁的情况下在后面所述的烧成工序中能够产生高缩率比。因此,在这个成形工序中即使形成圆弧比所希望的磁铁更浅(中心角小)的成形体也能够在烧成后获得圆弧深的磁铁。
成形体的中心角优选根据铁氧体磁性材料的组成作适当设定,例如成形体的中心角能够被设定成比作为目标的磁铁的中心角小10~20%左右。
<烧成工序>
在烧成工序中烧成在成形工序制得的成形体从而以其作为烧结体。由此就可获得由如以上所述那样的铁氧体磁性材料的烧结体构成的磁铁1。在制造弧段形状的磁铁的情况下,在烧成中,以具有规定中心角的形式进行成形的成形体发生收缩,这时也就产生一定的缩率比。由此,所获得的烧结体成为具有比成形体更加小的中心角的烧结体。为了获得圆弧深的烧结体而优选烧成时的缩率比为1.0~2.5,更加优选为1.5~2.5。
烧成能够在大气中等氧化性气氛中进行。烧成温度优选为1050~1270℃,更加优选为1080~1240℃。另外,烧成时间(保持在烧成温度的时间)优选为0.5~3小时的程度。
此外,在以如以上所述那样的湿式成形来制得成形体的情况下,如果没有使这个成形体充分干燥,而就这样通过进行烧成来作急剧加热的话,那么就会有可能分散溶剂等发生急剧挥发从而在成形体上产生龟裂。因此,从避免像这样的不良状况的观点出发,优选通过在到达上述烧结温度之前,例如从室温到100℃左右以0.5℃/分钟程度的慢慢的升温速度进行加热来使成形体充分干燥,从而抑制龟裂的发生。此外,在添加表面活性剂(分散剂)等的情况下,例如优选在100~500℃左右的温度范围内通过以2.5℃/分钟左右的升温速度进行加热从而充分去除这些分散溶剂挥发物(脱脂处理)。此外,这些处理既可以在开始烧成工序的时候进行,也可以在烧成工序前以别的途径来进行。
以上虽然就有关铁氧体烧结磁铁的优选的制造方法作了说明,但是只要至少使用本发明的铁氧体磁性材料,那么制造方法并不限定于以上所述的制造方法,可以对以上所述条件等作适当变更。
另外,制造作为磁铁并不是铁氧体烧结磁铁而是粘结磁铁的情况下,例如在直至上述粉碎工序为止实行了各个加工工序之后,混合所获得的粉碎物和胶粘剂,通过在磁场中对该混合物加以成形从而就能够获得含有本发明的铁氧体磁性材料粉末的粘结磁铁。
实施例
以下是通过实施例来进一步详细地说明本发明,但是本发明并不限定于这些实施例。
[实施例1](铁氧体烧结磁铁的制造)
首先,作为铁氧体磁性材料的主要组成的原料准备氧化铁(Fe2O3)、碳酸钙(CaCO3)、碳酸锶(SrCO3)、氧化钴(Co3O4)、碳酸钡(BaCO3)以及氢氧化镧[La(OH)3],并以烧成后的主要组成成为以下所述组成式的形式分别对这些原料进行称量。另外,作为Si成分以相对于主要组成成为0.69质量%的形式准备氧化硅(SiO2)。
主要组成的组成式:Ca1-w-x-yLawSrxBayFezComO19
在实施例1中与表1所表示的那样以获得主要组成的原子比率分别不相同的铁氧体磁性材料的形式用多个组合来准备原料。该实施例1是一种特别让Ca(1-w-x-y=0.0333~0.6007)以及Sr(x=0.0003~0.5700)的原子比率发生大变化来制造试样1-1~1-9的各种铁氧体烧结磁铁的实施例。
以下是就有关使用以上所述原料的铁氧体烧结磁铁的制造方法加以说明。用湿式磨碎机对在上述称量后的原料中的主要组成的原料实施10分钟的混合、并粉碎,从而获得浆料(配合工序)。在干燥该浆料之后,在大气中以1250℃的温度条件保持2小时来实行预烧(预烧工序)。
用小型棒杆式振动研磨机对所获得的预烧粉末实施10分钟的粗粉碎。在这个粗粉碎材料中分别添加在上述内容中称量的氧化硅(SiO2);相对于粗粉碎材料成为1.90质量%的碳酸钙(CaCO3);成为0.45质量%的山梨醇。使用湿式球磨机对该混合物实行33小时的微分碎从而获得浆料(以上为粉碎工序)。
在微粉碎之后以固体成分浓度成为73~75%的形式调整所获得的浆料从而制得湿式成形用浆料。使用湿式磁场成形机在796kA/m(10kOe)的施加磁场中使该湿式成形用浆料成形,从而制得具有直径30mm×厚度15mm的圆柱状的成形体(成形工序)。所获得的成形体在大气中以室温条件进行充分干燥,接着在大气中以1200℃的温度条件实行保持1小时的烧成,由此而获得铁氧体烧结磁铁(烧成工序)。
(铁氧体烧结磁铁的评价)
在对由实施例1所获得的各个铁氧体烧结磁铁的圆柱的上下面实施加工之后,在使用最大施加磁场755kA/m(12kOe)的B-H跟踪器来求得这些Br(mT)以及HcJ(kA/m),并且测定Br成为90%的时候的外部磁场强度(Hk),据此而求得Hk/HcJ(%)。
所获得的结果被表示于表1中。
[表1]
从表1中可以明确如果Sr的比率(x)超过0.0003不到0.4545且Ca的比率(1-w-x-y)超过0.1487不到0.6007的话,那么既能够良好地维持Br以及HcJ又能够获得高Hk/HcJ。
[实施例2](铁氧体烧结磁铁的制造)
在实施例2中除了以获得如表2所示主要组成的原子比率分别不同的铁氧体磁性材料的形式准备多个组合的原料之外,其余均以与实施例1相同地来制造铁氧体烧结磁铁。该实施例2是一种特别以让La(w=0.1801~0.6621)的原子比率发生较大变化,伴随于此而使La/Co(w/m=0.72~2.65)发生变化的形式加以实施从而制造出试样2-1~2-9的各种铁氧体烧结磁铁的实施例。
(铁氧体烧结磁铁的评价)
使用由实施例2所获得的各个铁氧体烧结磁铁,与实施例1相同求得Br(mT)、HcJ(kA/m)以及Hk/HcJ(%)。所获得的结果被表示于表2中。
[表2]
从表2中可以明确如果La的比率(w)超过0.1801不到0.6621且La/Co(w/m)超过0.72不到2.65的话,那么既能够良好地维持Br以及HcJ又能够获得高Hk/HcJ。
[实施例3](铁氧体烧结磁铁的制造)
在实施例3中除了以获得如表3所示主要组成的原子比率分别不同的铁氧体磁性材料的形式准备多个组合的原料之外,其余均以与实施例1相同地来制造铁氧体烧结磁铁。该实施例3是一种特别以让Fe(z=7.80~12.10)的原子比率发生较大变化,从而制造出试样3-1~3-10的各种铁氧体烧结磁铁的实施例。
(铁氧体烧结磁铁的评价)
使用由实施例3所获得的各个铁氧体烧结磁铁,与实施例1相同地求得Br(mT)、HcJ(kA/m)以及Hk/HcJ(%)。所获得的结果被表示于表3中。
[表3]
从表3中可以明确如果Fe的比率(z)超过7.80不到11.40的话,那么既能够良好地维持Br以及HcJ又能够获得高Hk/HcJ。
[实施例4](铁氧体烧结磁铁的制造)
在实施例4中除了以获得如表4所示主要组成的原子比率分别不同的铁氧体磁性材料的形式准备多个组合的原料之外,其余均以与实施例1相同地来制造铁氧体烧结磁铁。该实施例4是一种特别以让Co(m=0.00~0.70)的原子比率发生较大变化,伴随于此而使Co/Fe(m/z=0.000~0.076)以及La/Co(w/m=0.564~3.589)发生变化的形式加以实施,从而制造出试样4-1~4-7的各种铁氧体烧结磁铁的实施例。
(铁氧体烧结磁铁的评价)
使用由实施例4所获得的各个铁氧体烧结磁铁,与实施例1相同地求得Br(mT)、HcJ(kA/m)以及Hk/HcJ(%)。所获得的结果被表示于表4中。
[表4]
从表4中可以明确如果Co/Fe(m/z)超过0.012不到0.65且La/Co(w/m)超过0.659不到3.589的话,那么既能够良好地维持Br以及HcJ又能够获得高Hk/HcJ。
[实施例5](铁氧体烧结磁铁的制造)
在实施例5中除了以获得如表5所示主要组成的原子比率分别不同的铁氧体磁性材料的形式准备多个组合的原料之外,其余均以与实施例1相同地来制造铁氧体烧结磁铁。该实施例5是一种特别以让Ba(y=0.0002~0.0150)的原子比率发生较大变化,从而制造出试样5-1~5-11的各种铁氧体烧结磁铁的实施例。
(铁氧体烧结磁铁的评价)
使用由实施例5所获得的各个铁氧体烧结磁铁,与实施例1相同地求得Br(mT)、HcJ(kA/m)以及Hk/HcJ(%)。
另外,关于各个铁氧体烧结磁铁,分别求得这些铁氧体烧结磁铁的制造烧成时的成形体的收缩比例、厚度[shh(%)=100-(烧结体的厚度/成形体的厚度)×100]以及直径[shφ(%)=100-(烧结体的直径/成形体的直径)×100],据此计算出烧结前后的缩率比(shh/shφ:c轴方向/a轴方向)。所获得的结果被集中表示于表5中。
[表5]
从表5中可以明确如果Ba的比率(y)超过0.0002不到0.0110的话,那么既能够良好地维持Br以及HcJ又能够获得高Hk/HcJ,除此之外能够获得高缩率比。另外,Sr比率(x)较Ba的比率(y)来得小的试样5-11特别是在Br和Hk/HcJ这两点上不够充分,并进一步证实了缩率比与满足y<x的条件的其它试样相比较相对较小。
[实施例6](铁氧体烧结磁铁的制造)
在实施例6中除了如同表6所表示的那样以构成铁氧体烧结磁铁的铁氧体磁性材料的构成元素的比例(摩尔%)各自不相同的形式,准备多个组合的原料之外,以与实施例1相同地制造铁氧体烧结磁铁。各个构成元素的比例(摩尔%)是将整体作为100%从而使换算成各个元素的分别由表6所表示的氧化物的时侯的含量规格化的值。该实施例6是一种特别是以让Si成分(SiO2)的含量发生较大变化从而伴随于此“[(Ca+R+Sr+Ba)-(Fe+M)/12]/Si”的值发生变化的形式加以实施来制造试样6-1~6-5的各种铁氧体烧结磁铁的实施例。
(铁氧体烧结磁铁的评价)
使用由实施例6所获得的各个铁氧体烧结磁铁,与实施例1相同地求得Br(mT)、HcJ(kA/m)以及Hk/HcJ(%)。所获得的结果被表示于表6中。
[表6]
如表6所示可以明确如果[(Ca+R+Sr+Ba)-(Fe+M)/12]/Si超过1.43不到3.58的话,那么既能够良好地维持Br以及HcJ又能够获得高Hk/HcJ。
[实施例7](缩率比的测定)
首先,除了以主要组成中的Ba的原子比率(y)成为0.0002以及0.0045的形式进行调整之外,其余均以与实施例1相同的方法制作圆柱状的铁氧体烧结磁铁。关于各个铁氧体烧结磁铁,分别求得烧成时的成形体的收缩比例、厚度[shh(%)=100-(烧结体的厚度/成形体的厚度)×100]以及直径[shφ(%)=100-(烧结体的直径/成形体的直径)×100],据此计算出烧结前后的缩率比(shh/shφ:c轴方向/a轴方向)。
(弧段型铁氧体烧结磁铁的制作)
与此同时,分别制作由与这相同的铁氧体磁性材料构成的由图1所表示的弧段型铁氧体烧结磁铁。具体是除了在制得各个湿式成形用浆料之后以获得弧段形状的形式进行成形工序之外,其余以与实施例1相同的方法制得铁氧体烧结磁铁。
在实施例7中,即便是在使用以上所述2种铁氧体磁性材料中的任一种的情况下,也能够以获得如表7所表示那样的相同烧结体尺寸的形式分别调整成形体尺寸。关于为了使用各个铁氧体磁性材料来制得相同烧结体尺寸而必要的成形体尺寸被表示于表7中。表7中的OR、IR、宽度以及长度的各个尺寸分别是图2所表示的部分的尺寸。另外,在表7中,shh(%)、shφ以及shh/shφ是用由所分别对应的铁氧体磁性材料构成的圆柱状的铁氧体烧结磁铁来测定的时候的值。
[表7]
如表7所示可以证实:在形成相同尺寸的烧结体的情况下,Ba的原子比率高,即,如果Ba置换到A位点(site)的置换量大的话,那么能够增大缩率比,为了获得具有规定中心角的铁氧体烧结磁铁,能够使用中心角更加小的成形体。
[实施例8]
除了如表8所表示的那样改变作为目标的烧结体的尺寸之外,其余均以与实施例7相同地制作由2种铁氧体磁性材料构成的铁氧体烧结磁铁,此时,求得为了获得相同烧结体尺寸而成为必要的各个成形体的尺寸。所获得的结果被表示于表8中。
[表8]
如表8所示可以证实:在形成相同尺寸的烧结体的情况下,Ba的置换量大的铁氧体磁性材料的这一方能够使用中心角小的成形体。
[实施例9]
除了如表9所表示的那样改变作为目标的烧结体的尺寸之外,其余以与实施例7相同地来制造由2种铁氧体磁性材料构成的铁氧体烧结磁铁,此时求得为了获得相同烧结体尺寸而必要的各个成形体尺寸。另外,分别对使用各个铁氧体磁性材料的烧结体的制造实行10000次,对其中在烧结体上发生龟裂的次数进行计数,并在成形工序中求得对于将湿式成形用浆料充填于模具来说所需要的平均时间。所获得的结果被表示于表9中。
[表9]
如表9所示可以证实在形成相同尺寸的烧结体的情况下,Ba的置换量大的铁氧体磁性材料的这一方能够使用中心角小的成形体。另外,可以明确Ba的置换量大的铁氧体磁性材料的这一方,能够减少在制造中心角大的烧结体的时候的龟裂而且还能够缩短成形时的充填时间。
Claims (17)
1.一种铁氧体磁性材料,其特征在于,
是一种具备由铁氧体相构成的主相的铁氧体磁性材料,所述铁氧体相具有六方晶结构,
具有由下式(1)所表示的主要组成,
Ca1-w-x-yRwSrxBayFezMmO19(1)
式(1)中,R是选自稀土类元素以及Bi中的至少1种元素且至少含有La,该稀土类元素包含Y,M是选自Co、Mn、Mg、Ni、Cu以及Zn中的至少1种元素且至少含有Co,
在所述式(1)中w、x、y、z以及m满足下式(2)、(3)、(4)、(5)、(6)、(7)以及(8),
0.25<w<0.65(2)
0.1011≤x≤0.15(3)
0.0002<y<0.011(4)
y<x(5)
8<z<11(6)
1.0<w/m<2.5(7)
0.017<m/z<0.065(8)
所述主要组成中的Ca的原子比率(1-w-x-y)为0.4535≤(1-w-x-y)≤0.5006,
作为副成分至少含有Si成分,该Si成分的总量相对于所述主要组成为0.1~3质量%,并且
Ca、R、Sr、Ba、Fe、M以及Si的摩尔比满足下式(9),
1.5≤[(Ca+R+Sr+Ba)-(Fe+M)/12]/Si≤3.5(9)。
2.如权利要求1所述的铁氧体磁性材料,其特征在于,
所述w满足下式(2a)
0.3≤w≤0.55(2a)。
3.如权利要求1所述的铁氧体磁性材料,其特征在于,
所述w满足下式(2aa)
0.3494≤w≤0.4414(2aa)。
4.如权利要求1所述的铁氧体磁性材料,其特征在于,
所述y满足下式(4a)
0.0006≤y≤0.010(4a)。
5.如权利要求1所述的铁氧体磁性材料,其特征在于,
所述y满足下式(4aa)
0.0006≤y≤0.0063(4aa)。
6.如权利要求1所述的铁氧体磁性材料,其特征在于,
所述z满足下式(6a)
8.5≤z≤10.5(6a)。
7.如权利要求1所述的铁氧体磁性材料,其特征在于,
所述z满足下式(6aa)
9.01≤z≤9.71(6aa)。
8.如权利要求1所述的铁氧体磁性材料,其特征在于,
所述w/m满足下式(7a)
1.2≤w/m≤2.0(7a)。
9.如权利要求1所述的铁氧体磁性材料,其特征在于,
所述w/m满足下式(7aa)
1.066≤w/m≤1.586(7aa)。
10.如权利要求1所述的铁氧体磁性材料,其特征在于,
所述m/z满足下式(8a)
0.02≤m/z≤0.05(8a)。
11.如权利要求1所述的铁氧体磁性材料,其特征在于,
所述m/z满足下式(8aa)
0.022≤m/z≤0.040(8aa)。
12.如权利要求1所述的铁氧体磁性材料,其特征在于,
Ca、R、Sr、Ba、Fe、M、以及Si的摩尔比满足下式(9a)
1.79≤[(Ca+R+Sr+Ba)-(Fe+M)/12]/Si≤2.39(9a)。
13.一种铁氧体烧结磁铁,其特征在于,
由权利要求1~12中任意一项所述的铁氧体磁性材料构成。
14.一种磁铁,其特征在于,
由权利要求1所述的铁氧体磁性材料所构成并具有弧段形状而且该形状的中心角为30°以上。
15.如权利要求14所述的磁铁,其特征在于,
所述中心角为57.5°以上。
16.如权利要求14所述的磁铁,其特征在于,
所述中心角为60°以上。
17.如权利要求14所述的磁铁,其特征在于,
所述中心角为130.4°以上。
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