CN106495230A - A kind of preparation method of Barium hexaferrite - Google Patents

A kind of preparation method of Barium hexaferrite Download PDF

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Publication number
CN106495230A
CN106495230A CN201610989501.6A CN201610989501A CN106495230A CN 106495230 A CN106495230 A CN 106495230A CN 201610989501 A CN201610989501 A CN 201610989501A CN 106495230 A CN106495230 A CN 106495230A
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China
Prior art keywords
barium hexaferrite
barium
hexaferrite
xerogel
obtains
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CN201610989501.6A
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Chinese (zh)
Inventor
张达明
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Wuxi Mingsheng Strong Blower Co Ltd
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Wuxi Mingsheng Strong Blower Co Ltd
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Priority to CN201610989501.6A priority Critical patent/CN106495230A/en
Publication of CN106495230A publication Critical patent/CN106495230A/en
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    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G49/00Compounds of iron
    • C01G49/0018Mixed oxides or hydroxides
    • C01G49/0036Mixed oxides or hydroxides containing one alkaline earth metal, magnesium or lead
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2002/00Crystal-structural characteristics
    • C01P2002/70Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/60Particles characterised by their size
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00Physical properties of inorganic compounds
    • C01P2006/42Magnetic properties

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Geology (AREA)
  • Inorganic Chemistry (AREA)
  • Hard Magnetic Materials (AREA)
  • Compounds Of Iron (AREA)

Abstract

The invention discloses a kind of preparation method of Barium hexaferrite, including:(1) according to mol ratio 1:12:Barium nitrate, ferric nitrate and citric acid are mixed and form aqueous solution by the ratio of (6 26);(2) ammonia is added in solution, and up to pH 47,85 95 DEG C of water-bath heated at constant temperature 13 hours reacts which;(3) reactant is dried, obtains xerogel;(5) xerogel is calcined at 550 750 DEG C, is incubated 13 hours, obtains BaFe12O19Barium hexaferrite.Through X ray diffracting spectrum, show that the Barium hexaferrite that the present invention is prepared is Magnetoplumbate-type hexagonal Barium hexaferrite BaFe12O19.Its piece footpath is 8 26 μm, soilless sticking phenomenon.Its coercivity H is more than 368kA/m, the 200kA/m of Barium hexaferrite prepared far above additive method or so.

Description

A kind of preparation method of Barium hexaferrite
Technical field
A kind of the present invention relates to technical field of magnetic materials, more particularly to preparation method of Barium hexaferrite.
Background technology
At present, used by absorbing material, the main body of absorbent development is still magnetic material, the high speed development of information technology so that Ferrite magnetic material is more widely used, and wherein hexagonal crystal system Barium hexaferrite becomes people with its excellent Frequency Response The emphasis of Recent study.Since World War II, especially developed country puts into substantial amounts of manpower and materials to carry out in succession for countries in the world The research of absorbing material.In recent years, with the continuous development of electromagnetic technique, electromagnetic radiation is also more and more full of in ours Life sky asks, therefore civilian absorbing material oneself widely paid close attention to.At present, the research of microwave absorbing material it is critical only that system Standby go out absorbance height, thin coating, absorption band width, light weight, high temperature resistant, anti scuffing and low cost microwave absorbing material.
Content of the invention
It is an object of the invention to proposing a kind of preparation method of Barium hexaferrite so that the Barium hexaferrite performance for preparing Excellent, possess more preferable absorbing property.
It is that the present invention is employed the following technical solutions up to this purpose:
A kind of preparation method of Barium hexaferrite, including:
(1) according to mol ratio 1:12:(6-26) barium nitrate, ferric nitrate and citric acid are mixed and are formed water-soluble by ratio Liquid;
(2) ammonia is added in solution, and up to pH 4-7,85-95 DEG C of heated at constant temperature 1-3 hour of water-bath reacts which;
(3) reactant is dried, obtains xerogel;
(5) xerogel is calcined at 550-750 DEG C, is incubated 1-3 hours, obtains BaFe12O19Barium hexaferrite.
Through X ray diffracting spectrum, show that the Barium hexaferrite that the present invention is prepared is Magnetoplumbate-type hexagonal Barium hexaferrite BaFe12O19.Its piece footpath is 8-26 μm, soilless sticking phenomenon.Its coercivity H is more than 368kA/m, prepares far above additive method 200kA/m of Barium hexaferrite for obtaining or so.As coercivity is bigger, magnetic loss is stronger, and therefore absorbing property is better, therefore originally The Barium hexaferrite that invention is prepared possesses more excellent suction ripple energy-absorbing.
Specific embodiment
Technical scheme is further illustrated below by specific embodiment.
Embodiment 1
A kind of preparation method of Barium hexaferrite, including:
(1) according to mol ratio 1:12:Barium nitrate, ferric nitrate and citric acid are mixed and form aqueous solution by 6 ratio;
(2) ammonia is added in solution, and up to pH 4,85 DEG C of water-bath heated at constant temperature 1 hour reacts which;
(3) reactant is dried, obtains xerogel;
(5) xerogel is calcined at 550 DEG C, is incubated 1 hour, obtains BaFe12O19Barium hexaferrite.
Embodiment 2
A kind of preparation method of Barium hexaferrite, including:
(1) according to mol ratio 1:12:Barium nitrate, ferric nitrate and citric acid are mixed and form aqueous solution by 26 ratio;
(2) ammonia is added in solution, and up to pH 7,95 DEG C of water-bath heated at constant temperature 3 hours reacts which;
(3) reactant is dried, obtains xerogel;
(5) xerogel is calcined at 750 DEG C, is incubated 3 hours, obtains BaFe12O19Barium hexaferrite.
Embodiment 3
A kind of preparation method of Barium hexaferrite, including:
(1) according to mol ratio 1:12:Barium nitrate, ferric nitrate and citric acid are mixed and form aqueous solution by 15 ratio;
(2) ammonia is added in solution, and up to pH 6,90 DEG C of water-bath heated at constant temperature 2 hours reacts which;
(3) reactant is dried, obtains xerogel;
(5) xerogel is calcined at 650 DEG C, is incubated 2 hours, obtains BaFe12O19Barium hexaferrite.
Through X ray diffracting spectrum, show that the Barium hexaferrite that embodiment 1-3 is prepared is Magnetoplumbate-type hexagonal Barium hexaferrite BaFe12O19.Its piece footpath is 8-26 μm, soilless sticking phenomenon.Its coercivity H is more than 368kA/m, prepares far above additive method 200kA/m of Barium hexaferrite for obtaining or so.

Claims (1)

1. a kind of preparation method of Barium hexaferrite, including:
(1) according to mol ratio 1:12:(6-26) barium nitrate, ferric nitrate and citric acid are mixed and form aqueous solution by ratio;
(2) ammonia is added in solution, and up to pH 4-7,85-95 DEG C of heated at constant temperature 1-3 hour of water-bath reacts which;
(3) reactant is dried, obtains xerogel;
(5) xerogel is calcined at 550-750 DEG C, is incubated 1-3 hours, obtains BaFe12O19Barium hexaferrite.
CN201610989501.6A 2016-11-10 2016-11-10 A kind of preparation method of Barium hexaferrite Pending CN106495230A (en)

Priority Applications (1)

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CN201610989501.6A CN106495230A (en) 2016-11-10 2016-11-10 A kind of preparation method of Barium hexaferrite

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Application Number Priority Date Filing Date Title
CN201610989501.6A CN106495230A (en) 2016-11-10 2016-11-10 A kind of preparation method of Barium hexaferrite

Publications (1)

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CN106495230A true CN106495230A (en) 2017-03-15

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111298795A (en) * 2020-03-19 2020-06-19 六盘水师范学院 Performance optimization method of strontium titanate magnetic photocatalyst
CN114686168A (en) * 2020-12-30 2022-07-01 洛阳尖端技术研究院 Flaky ferrite wave-absorbing material, flaky ferrite/carbon composite wave-absorbing material, and preparation method and application thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1880272A (en) * 2005-06-16 2006-12-20 中国科学院金属研究所 Hexagonal sheet-like barium ferrite magnetic nanometer powder preparation method
CN102485692A (en) * 2010-12-06 2012-06-06 沈阳理工大学 Preparation method of two-dimensional sheet-shaped barium ferrite

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1880272A (en) * 2005-06-16 2006-12-20 中国科学院金属研究所 Hexagonal sheet-like barium ferrite magnetic nanometer powder preparation method
CN102485692A (en) * 2010-12-06 2012-06-06 沈阳理工大学 Preparation method of two-dimensional sheet-shaped barium ferrite

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
刘俊丰: ""溶胶-凝胶法吸波材料钡铁氧体BaFe12O19的制备"", 《中国优秀硕士学位论文全文数据库 工程科技II辑》 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111298795A (en) * 2020-03-19 2020-06-19 六盘水师范学院 Performance optimization method of strontium titanate magnetic photocatalyst
CN114686168A (en) * 2020-12-30 2022-07-01 洛阳尖端技术研究院 Flaky ferrite wave-absorbing material, flaky ferrite/carbon composite wave-absorbing material, and preparation method and application thereof

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