CN102584193B - Preparation method of bismuth ferrate barium titanate solid solution composite material with high magnetization intensity and high polarization intensity - Google Patents

Preparation method of bismuth ferrate barium titanate solid solution composite material with high magnetization intensity and high polarization intensity Download PDF

Info

Publication number
CN102584193B
CN102584193B CN 201210023356 CN201210023356A CN102584193B CN 102584193 B CN102584193 B CN 102584193B CN 201210023356 CN201210023356 CN 201210023356 CN 201210023356 A CN201210023356 A CN 201210023356A CN 102584193 B CN102584193 B CN 102584193B
Authority
CN
China
Prior art keywords
powder
barium titanate
hours
matrix material
biy
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
CN 201210023356
Other languages
Chinese (zh)
Other versions
CN102584193A (en
Inventor
林营
杨海波
杨艳艳
朱建锋
王芬
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shaanxi University of Science and Technology
Original Assignee
Shaanxi University of Science and Technology
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Shaanxi University of Science and Technology filed Critical Shaanxi University of Science and Technology
Priority to CN 201210023356 priority Critical patent/CN102584193B/en
Publication of CN102584193A publication Critical patent/CN102584193A/en
Application granted granted Critical
Publication of CN102584193B publication Critical patent/CN102584193B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Abstract

The invention provides a preparation method of a bismuth ferrate barium titanate solid solution composite material with high magnetization intensity and high polarization intensity. BiY2Fe5O12 powder and 0.7BiFeO3-0.3BaTiO3 powder are prepared; the 0.7BiFeO3-0.3BaTiO3 powder is evenly mixed with the BiY2Fe5O12 powder, and then a polyvinyl alcohol (PVA) adhesive is added to an obtained mixture to obtain mixed powder of the needed composite material; and the mixed powder of the composite material is pressed to be formed according to requirements, heated to remove the adhesive PVA, and then sintered to ceramic to obtain the bismuth ferrate barium titanate solid solution composite material with high magnetization intensity and high resistivity. By adopting the preparation method, the saturation magnetization intensity of bismuth ferrate barium titanate solid solution ceramic can be increased from 0.03emu/g to 4.4emu/g; and meanwhile, the remnant polarization intensity of the bismuth ferrate barium titanate solid solution ceramic can be obviously increased from 18.6 C/cm2 to 20.1 C/cm2.

Description

The preparation method of the ferrous acid bismuth barium titanate sosoloid matrix material of a kind of high magnetic intensity and polarizability
Technical field
The invention belongs to material science, be specifically related to the preparation method of the ferrous acid bismuth barium titanate sosoloid matrix material of a kind of high magnetic intensity and polarizability.
Background technology
Multi-ferroic material (multiferroic) is a kind ofly to integrate ferroelectric, magnetic order, thus ferroelectricity and magnetic coexistence and material with magneto-electric coupled character.This material complementation pure (anti--) ferroelectric or (anti--) ferromagnetic material deficiency and present the order of electricity and magnetic simultaneously, because the coexistence of ferroelectricity and magnetic makes this material to be induced by electric field and produces magnetic field, iron electric polarization also can be brought out in magnetic field simultaneously, and this character is called as magnetoelectric effect.Electric field can be induced magnetic polarization, and magnetic field can be induced this special functional materials of iron electric polarization will have widely and be used, and concrete the application is mainly reflected in following several respects: modulate mutually to amplitude, polarization and the position of light wave (1); (2) magnetoelectricity data storage and conversion; (3) optical diode; (4) spin wave producer; (5) amplification of spin wave and frequency inverted; (6) wide band magnetic detection and multi-function electronic device such as transmitter, stopper, inductor block, transmodulator etc.; (7) electric current, voltage bidirectional transducer etc.The ferrous acid bismuth is as a kind of typical single phase multi-iron material, have Curie temperature and Ne﹠1﹠el temperature far above room temperature, be present unique single phase multi-iron material that has ferroelectricity and parasitic weak ferromagnetism at ambient temperature simultaneously, therefore, caused numerous investigators' very big concern.Yet the shortcoming of ferrous acid bismuth is that the existence owing to ferrous ion and oxygen room causes big leakage conductance electric current and owing to antiferroelectric essence causes weak magnetic.Above shortcoming has seriously limited the practical application of ferrous acid bismuth material.Though, in the ferrous acid bismuth, introduce barium titanate formation sosoloid and can reduce its leakage current raising ferroelectricity to a certain extent.But the magnetic of the ferrous acid bismuth barium titanate sosoloid that forms still a little less than.Introducing ferromagnetic ferrite in ferrous acid bismuth pottery can significantly improve, yet, because vectolite (CoFe commonly used 2O 4) and the resistivity of nickel-zinc ferrite (NiZn ferrite) lower, if being incorporated into above ferrous acid bismuth barium titanate sosoloid, these two kinds of ferrites form matrix material, though can improve the magnetic property of ferrous acid bismuth barium titanate sosoloid, further reduce polarizability and worsen ferroelectricity thereby can reduce its resistivity.
Summary of the invention
The object of the present invention is to provide the preparation method of the ferrous acid bismuth barium titanate sosoloid matrix material of simple high magnetic intensity of a kind of preparation technology and polarizability.
For achieving the above object, the technical solution used in the present invention is:
1) by the chemical general formula BiY that mixes bismuth ferrous acid yttrium 2Fe 5O 12, take by weighing analytically pure Bi 2O 3, Y 2O 3, and Fe 2O 3Preparation back ball milling 4 hours, oven dry is sieved then, and briquetting through 900 ℃ of pre-burnings 3 hours, was pulverized 120 mesh sieves with the gained bulk sample then and was obtained BiY 2Fe 5O 12Powder;
2) press the chemical general formula 0.7BiFeO of ferrous acid bismuth barium titanate sosoloid 3-0.3BaTiO 3, take by weighing analytically pure BaCO 3, TiO 2, Bi 2O 3And Fe 2O 3Preparation back ball milling 4 hours, oven dry is sieved then, and briquetting through 840 ℃ of pre-burnings 3 hours, is crossed 120 mesh sieves after then the gained bulk sample being pulverized and is obtained 0.7BiFeO 3-0.3BaTiO 3Powder;
3) press chemical general formula xBiY 2Fe 5O 12/ (1-x) (0.7BiFeO 3-0.3BaTiO 3) with 0.7BiFeO 3-0.3BaTiO 3Powder and BiY 2Fe 5O 12Powder mixes, and wherein x is BiY 2Fe 5O 12Mass percent, and 0.05≤x≤0.2;
4) the PVA tackiness agent that adds mixed powder quality 8%~15% in mixed powder obtains the mixed powder of required matrix material;
5) with the mixed powder compression moulding on demand of matrix material, at 550 ℃, be incubated 4 hours and get rid of tackiness agent PVA, became porcelain in 0.5~2 hour, obtain the ferrous acid bismuth barium titanate sosoloid matrix material of high magnetic intensity and polarizability at 1000~1050 ℃ of following sintering.
It is 5% polyvinyl alcohol water solution granulation after 60 orders and 120 eye mesh screens sieve makes that described PVA tackiness agent adopts mass concentration.
The present invention can be increased to 4.4emu/g from the 0.03emu/ gram with the saturation magnetization of ferrous acid bismuth barium titanate solid solution ceramic.Simultaneously, can with the remnant polarization of ferrous acid bismuth barium titanate solid solution ceramic from 18.6 microcoulombs/centimetre 2Be increased to 20.1 microcoulombs/centimetre 2
Description of drawings
Fig. 1 is incubated 0.5 hour sintering gained pure phase 0.7BiFeO down at 1000 ℃ 3-0.3BaTiO 3The magnetic hysteresis loop of pottery.
Fig. 2 works as 0.7BiFeO 3-0.3BaTiO 3Mass ratio be 95%, BiY 2Fe 5O 12Mass ratio be 5%, 1050 ℃ the insulation 0.5 hour sintering gained matrix material magnetic hysteresis loops.
Fig. 3 works as 0.7BiFeO 3-0.3BaTiO 3Mass ratio be 90%, BiY 2Fe 5O 12Mass ratio be 10%, 1050 ℃ the insulation 1 hour sintering gained matrix material magnetic hysteresis loops.
Fig. 4 works as 0.7BiFeO 3-0.3BaTiO 3Mass ratio be 80%, BiY 2Fe 5O 12Mass ratio be 20%, 1050 ℃ the insulation 2 hours sintering gained matrix materials magnetic hysteresis loops.
Fig. 5 is incubated 0.5 hour pure 0.7BiFeO of sintering gained down at 1000 ℃ 3-0.3BaTiO 3The ferroelectric hysteresis loop of pottery.
Fig. 6 works as 0.7BiFeO 3-0.3BaTiO 3Mass ratio be 95%, BiY 2Fe 5O 12Mass ratio be 5%, 1050 ℃ the insulation 0.5 hour sintering gained matrix material ferroelectric hysteresis loops.
Fig. 7 works as 0.7BiFeO 3-0.3BaTiO 3Mass ratio be 90%, BiY 2Fe 5O 12Mass ratio be 10%, 1050 ℃ the insulation 1 hour sintering gained matrix material ferroelectric hysteresis loops.
Fig. 8 works as 0.7BiFeO 3-0.3BaTiO 3Mass ratio be 80%, BiY 2Fe 5O 12Mass ratio be 20%, 1000 ℃ the insulation 2 hours sintering gained matrix materials ferroelectric hysteresis loops.
Embodiment
Below in conjunction with drawings and Examples the present invention is described in further detail.
Embodiment 1:
1) by the chemical general formula BiY that mixes bismuth ferrous acid yttrium 2Fe 5O 12, take by weighing analytically pure Bi 2O 3, Y 2O 3, and Fe 2O 3Preparation back ball milling 4 hours, oven dry is sieved then, and briquetting through 900 ℃ of pre-burnings 3 hours, was pulverized 120 mesh sieves with the gained bulk sample then and was obtained BiY 2Fe 5O 12Powder;
2) press the chemical general formula 0.7BiFeO of ferrous acid bismuth barium titanate sosoloid 3-0.3BaTiO 3, take by weighing analytically pure BaCO 3, TiO 2, Bi 2O 3And Fe 2O 3Preparation back ball milling 4 hours, oven dry is sieved then, and briquetting through 840 ℃ of pre-burnings 3 hours, is crossed 120 mesh sieves after then the gained bulk sample being pulverized and is obtained 0.7BiFeO 3-0.3BaTiO 3Powder;
3) press chemical general formula xBiY 2Fe 5O 12/ (1-x) (0.7BiFeO 3-0.3BaTiO 3) with 0.7BiFeO 3-0.3BaTiO 3Powder and BiY 2Fe 5O 12Powder mixes, and wherein x is BiY 2Fe 5O 12Mass percent, and x=0.05;
4) the PVA tackiness agent that adds mixed powder quality 8% in mixed powder obtains the mixed powder of required matrix material;
It is 5% polyvinyl alcohol water solution granulation after 60 orders and 120 eye mesh screens sieve makes that described PVA tackiness agent adopts mass concentration;
5) with the mixed powder compression moulding on demand of matrix material,, be incubated 4 hours and get rid of tackiness agent PVA, became porcelain in 0.5 hour, obtain the ferrous acid bismuth barium titanate sosoloid matrix material of high magnetic intensity and polarizability at 1050 ℃ of following sintering at 550 ℃.
As seen from Figure 1 the magnetic of pure phase bismuth ferric barium titanate solid solution ceramic very a little less than, saturation magnetization is a 0.03emu/ gram.The saturation magnetization of this matrix material is 1.1emu/g as seen from Figure 2.
Embodiment 2:
1) by the chemical general formula BiY that mixes bismuth ferrous acid yttrium 2Fe 5O 12, take by weighing analytically pure Bi 2O 3, Y 2O 3, and Fe 2O 3Preparation back ball milling 4 hours, oven dry is sieved then, and briquetting through 900 ℃ of pre-burnings 3 hours, was pulverized 120 mesh sieves with the gained bulk sample then and was obtained BiY 2Fe 5O 12Powder;
2) press the chemical general formula 0.7BiFeO of ferrous acid bismuth barium titanate sosoloid 3-0.3BaTiO 3, take by weighing analytically pure BaCO 3, TiO 2, Bi 2O 3And Fe 2O 3Preparation back ball milling 4 hours, oven dry is sieved then, and briquetting through 840 ℃ of pre-burnings 3 hours, is crossed 120 mesh sieves after then the gained bulk sample being pulverized and is obtained 0.7BiFeO 3-0.3BaTiO 3Powder;
3) press chemical general formula xBiY 2Fe 5O 12/ (1-x) (0.7BiFeO 3-0.3BaTiO 3) with 0.7BiFeO 3-0.3BaTiO 3Powder and BiY 2Fe 5O 12Powder mixes, and wherein x is BiY 2Fe 5O 12Mass percent, and x=0.1;
4) the PVA tackiness agent that adds mixed powder quality 10% in mixed powder obtains the mixed powder of required matrix material;
It is 5% polyvinyl alcohol water solution granulation after 60 orders and 120 eye mesh screens sieve makes that described PVA tackiness agent adopts mass concentration;
5) with the mixed powder compression moulding on demand of matrix material,, be incubated 4 hours and get rid of tackiness agent PVA, became porcelain in 1 hour, obtain the ferrous acid bismuth barium titanate sosoloid matrix material of high magnetic intensity and polarizability at 1050 ℃ of following sintering at 550 ℃.
The saturation magnetization of matrix material is the 2.1emu/ gram at this moment as seen from Figure 3.
Embodiment 3:
1) by the chemical general formula BiY that mixes bismuth ferrous acid yttrium 2Fe 5O 12, take by weighing analytically pure Bi 2O 3, Y 2O 3, and Fe 2O 3Preparation back ball milling 4 hours, oven dry is sieved then, and briquetting through 900 ℃ of pre-burnings 3 hours, was pulverized 120 mesh sieves with the gained bulk sample then and was obtained BiY 2Fe 5O 12Powder;
2) press the chemical general formula 0.7BiFeO of ferrous acid bismuth barium titanate sosoloid 3-0.3BaTiO 3, take by weighing analytically pure BaCO 3, TiO 2, Bi 2O 3And Fe 2O 3Preparation back ball milling 4 hours, oven dry is sieved then, and briquetting through 840 ℃ of pre-burnings 3 hours, is crossed 120 mesh sieves after then the gained bulk sample being pulverized and is obtained 0.7BiFeO 3-0.3BaTiO 3Powder;
3) press chemical general formula xBiY 2Fe 5O 12/ (1-x) (0.7BiFeO 3-0.3BaTiO 3) with 0.7BiFeO 3-0.3BaTiO 3Powder and BiY 2Fe 5O 12Powder mixes, and wherein x is BiY 2Fe 5O 12Mass percent, and x=0.2;
4) the PVA tackiness agent that adds mixed powder quality 12% in mixed powder obtains the mixed powder of required matrix material;
It is 5% polyvinyl alcohol water solution granulation after 60 orders and 120 eye mesh screens sieve makes that described PVA tackiness agent adopts mass concentration;
5) with the mixed powder compression moulding on demand of matrix material,, be incubated 4 hours and get rid of tackiness agent PVA, became porcelain in 2 hours, obtain the ferrous acid bismuth barium titanate sosoloid matrix material of high magnetic intensity and polarizability at 1050 ℃ of following sintering at 550 ℃.
The saturation magnetization of matrix material is the 4.4emu/ gram at this moment as seen from Figure 4.
Embodiment 4:
1) by the chemical general formula BiY that mixes bismuth ferrous acid yttrium 2Fe 5O 12, take by weighing analytically pure Bi 2O 3, Y 2O 3, and Fe 2O 3Preparation back ball milling 4 hours, oven dry is sieved then, and briquetting through 900 ℃ of pre-burnings 3 hours, was pulverized 120 mesh sieves with the gained bulk sample then and was obtained BiY 2Fe 5O 12Powder;
2) press the chemical general formula 0.7BiFeO of ferrous acid bismuth barium titanate sosoloid 3-0.3BaTiO 3, take by weighing analytically pure BaCO 3, TiO 2, Bi 2O 3And Fe 2O 3Preparation back ball milling 4 hours, oven dry is sieved then, and briquetting through 840 ℃ of pre-burnings 3 hours, is crossed 120 mesh sieves after then the gained bulk sample being pulverized and is obtained 0.7BiFeO 3-0.3BaTiO 3Powder;
3) press chemical general formula xBiY 2Fe 5O 12/ (1-x) (0.7BiFeO 3-0.3BaTiO 3) with 0.7BiFeO 3-0.3BaTiO 3Powder and BiY 2Fe 5O 12Powder mixes, and wherein x is BiY 2Fe 5O 12Mass percent, and x=0.05;
4) the PVA tackiness agent that adds mixed powder quality 15% in mixed powder obtains the mixed powder of required matrix material;
It is 5% polyvinyl alcohol water solution granulation after 60 orders and 120 eye mesh screens sieve makes that described PVA tackiness agent adopts mass concentration;
5) with the mixed powder compression moulding on demand of matrix material,, be incubated 4 hours and get rid of tackiness agent PVA, became porcelain in 1 hour, obtain the ferrous acid bismuth barium titanate sosoloid matrix material of high magnetic intensity and polarizability at 1050 ℃ of following sintering at 550 ℃.
As seen from Figure 5 the remnant polarization of pure phase bismuth ferric barium titanate solid solution ceramic be 18.7 microcoulombs/centimetre 2
As seen from Figure 6 this moment matrix material remnant polarization be 20.1 microcoulombs/centimetre 2
Embodiment 5:
1) by the chemical general formula BiY that mixes bismuth ferrous acid yttrium 2Fe 5O 12, take by weighing analytically pure Bi 2O 3, Y 2O 3, and Fe 2O 3Preparation back ball milling 4 hours, oven dry is sieved then, and briquetting through 900 ℃ of pre-burnings 3 hours, was pulverized 120 mesh sieves with the gained bulk sample then and was obtained BiY 2Fe 5O 12Powder;
2) press the chemical general formula 0.7BiFeO of ferrous acid bismuth barium titanate sosoloid 3-0.3BaTiO 3, take by weighing analytically pure BaCO 3, TiO 2, Bi 2O 3And Fe 2O 3Preparation back ball milling 4 hours, oven dry is sieved then, and briquetting through 840 ℃ of pre-burnings 3 hours, is crossed 120 mesh sieves after then the gained bulk sample being pulverized and is obtained 0.7BiFeO 3-0.3BaTiO 3Powder;
3) press chemical general formula xBiY 2Fe 5O 12/ (1-x) (0.7BiFeO 3-0.3BaTiO 3) with 0.7BiFeO 3-0.3BaTiO 3Powder and BiY 2Fe 5O 12Powder mixes, and wherein x is BiY 2Fe 5O 12Mass percent, and x=0.1;
4) the PVA tackiness agent that adds mixed powder quality 9% in mixed powder obtains the mixed powder of required matrix material;
It is 5% polyvinyl alcohol water solution granulation after 60 orders and 120 eye mesh screens sieve makes that described PVA tackiness agent adopts mass concentration;
5) with the mixed powder compression moulding on demand of matrix material,, be incubated 4 hours and get rid of tackiness agent PVA, became porcelain in 1 hour, obtain the ferrous acid bismuth barium titanate sosoloid matrix material of high magnetic intensity and polarizability at 1050 ℃ of following sintering at 550 ℃.
As seen from Figure 7 this moment matrix material remnant polarization be 17.4 microcoulombs/centimetre 2
Embodiment 6:
1) by the chemical general formula BiY that mixes bismuth ferrous acid yttrium 2Fe 5O 12, take by weighing analytically pure Bi 2O 3, Y 2O 3, and Fe 2O 3Preparation back ball milling 4 hours, oven dry is sieved then, and briquetting through 900 ℃ of pre-burnings 3 hours, was pulverized 120 mesh sieves with the gained bulk sample then and was obtained BiY 2Fe 5O 12Powder;
2) press the chemical general formula 0.7BiFeO of ferrous acid bismuth barium titanate sosoloid 3-0.3BaTiO 3, take by weighing analytically pure BaCO 3, TiO 2, Bi 2O 3And Fe 2O 3Preparation back ball milling 4 hours, oven dry is sieved then, and briquetting through 840 ℃ of pre-burnings 3 hours, is crossed 120 mesh sieves after then the gained bulk sample being pulverized and is obtained 0.7BiFeO 3-0.3BaTiO 3Powder;
3) press chemical general formula xBiY 2Fe 5O 12/ (1-x) (0.7BiFeO 3-0.3BaTiO 3) with 0.7BiFeO 3-0.3BaTiO 3Powder and BiY 2Fe 5O 12Powder mixes, and wherein x is BiY 2Fe 5O 12Mass percent, and x=0.2;
4) the PVA tackiness agent that adds mixed powder quality 13% in mixed powder obtains the mixed powder of required matrix material;
It is 5% polyvinyl alcohol water solution granulation after 60 orders and 120 eye mesh screens sieve makes that described PVA tackiness agent adopts mass concentration;
5) with the mixed powder compression moulding on demand of matrix material,, be incubated 4 hours and get rid of tackiness agent PVA, became porcelain in 2 hours, obtain the ferrous acid bismuth barium titanate sosoloid matrix material of high magnetic intensity and polarizability at 1000 ℃ of following sintering at 550 ℃.
As seen from Figure 8 this moment matrix material remnant polarization be 14.8 microcoulombs/centimetre 2
Embodiment 7:
1) by the chemical general formula BiY that mixes bismuth ferrous acid yttrium 2Fe 5O 12, take by weighing analytically pure Bi 2O 3, Y 2O 3, and Fe 2O 3Preparation back ball milling 4 hours, oven dry is sieved then, and briquetting through 900 ℃ of pre-burnings 3 hours, was pulverized 120 mesh sieves with the gained bulk sample then and was obtained BiY 2Fe 5O 12Powder;
2) press the chemical general formula 0.7BiFeO of ferrous acid bismuth barium titanate sosoloid 3-0.3BaTiO 3, take by weighing analytically pure BaCO 3, TiO 2, Bi 2O 3And Fe 2O 3Preparation back ball milling 4 hours, oven dry is sieved then, and briquetting through 840 ℃ of pre-burnings 3 hours, is crossed 120 mesh sieves after then the gained bulk sample being pulverized and is obtained 0.7BiFeO 3-0.3BaTiO 3Powder;
3) press chemical general formula xBiY 2Fe 5O 12/ (1-x) (0.7BiFeO 3-0.3BaTiO 3) with 0.7BiFeO 3-0.3BaTiO 3Powder and BiY 2Fe 5O 12Powder mixes, and wherein x is BiY 2Fe 5O 12Mass percent, and x=0.08;
4) the PVA tackiness agent that adds mixed powder quality 11% in mixed powder obtains the mixed powder of required matrix material;
It is 5% polyvinyl alcohol water solution granulation after 60 orders and 120 eye mesh screens sieve makes that described PVA tackiness agent adopts mass concentration;
5) with the mixed powder compression moulding on demand of matrix material,, be incubated 4 hours and get rid of tackiness agent PVA, became porcelain in 0.5 hour, obtain ferrous acid bismuth barium titanate sosoloid matrix material at 1030 ℃ of following sintering at 550 ℃.
Embodiment 8:
1) by the chemical general formula BiY that mixes bismuth ferrous acid yttrium 2Fe 5O 12, take by weighing analytically pure Bi 2O 3, Y 2O 3, and Fe 2O 3Preparation back ball milling 4 hours, oven dry is sieved then, and briquetting through 900 ℃ of pre-burnings 3 hours, was pulverized 120 mesh sieves with the gained bulk sample then and was obtained BiY 2Fe 5O 12Powder;
2) press the chemical general formula 0.7BiFeO of ferrous acid bismuth barium titanate sosoloid 3-0.3BaTiO 3, take by weighing analytically pure BaCO 3, TiO 2, Bi 2O 3And Fe 2O 3Preparation back ball milling 4 hours, oven dry is sieved then, and briquetting through 840 ℃ of pre-burnings 3 hours, is crossed 120 mesh sieves after then the gained bulk sample being pulverized and is obtained 0.7BiFeO 3-0.3BaTiO 3Powder;
3) press chemical general formula xBiY 2Fe 5O 12/ (1-x) (0.7BiFeO 3-0.3BaTiO 3) with 0.7BiFeO 3-0.3BaTiO 3Powder and BiY 2Fe 5O 12Powder mixes, and wherein x is BiY 2Fe 5O 12Mass percent, and x=0.15;
4) the PVA tackiness agent that adds mixed powder quality 14% in mixed powder obtains the mixed powder of required matrix material;
It is 5% polyvinyl alcohol water solution granulation after 60 orders and 120 eye mesh screens sieve makes that described PVA tackiness agent adopts mass concentration;
5) with the mixed powder compression moulding on demand of matrix material,, be incubated 4 hours and get rid of tackiness agent PVA, became porcelain in 1.5 hours, obtain ferrous acid bismuth barium titanate sosoloid matrix material at 1020 ℃ of following sintering at 550 ℃.

Claims (2)

1. the preparation method of the ferrous acid bismuth barium titanate sosoloid matrix material of high magnetic intensity and polarizability is characterized in that may further comprise the steps:
1) by the chemical general formula BiY that mixes bismuth ferrous acid yttrium 2Fe 5O 12, take by weighing analytically pure Bi 2O 3, Y 2O 3, and Fe 2O 3Preparation back ball milling 4 hours, oven dry is sieved then, and briquetting through 900 ℃ of pre-burnings 3 hours, was pulverized 120 mesh sieves with the gained bulk sample then and was obtained BiY 2Fe 5O 12Powder;
2) press the chemical general formula 0.7BiFeO of ferrous acid bismuth barium titanate sosoloid 3-0.3BaTiO 3, take by weighing analytically pure BaCO 3, TiO 2, Bi 2O 3And Fe 2O 3Preparation back ball milling 4 hours, oven dry is sieved then, and briquetting through 840 ℃ of pre-burnings 3 hours, is crossed 120 mesh sieves after then the gained bulk sample being pulverized and is obtained 0.7BiFeO 3-0.3BaTiO 3Powder;
3) press chemical general formula xBiY 2Fe 5O 12/ (1-x) (0.7BiFeO 3-0.3BaTiO 3) with 0.7BiFeO 3-0.3BaTiO 3Powder and BiY 2Fe 5O 12Powder mixes, and wherein x is BiY 2Fe 5O 12Mass percent, and 0.05≤x≤0.2;
4) the PVA tackiness agent that adds mixed powder quality 8%~15% in mixed powder obtains the mixed powder of required matrix material;
5) with the mixed powder compression moulding on demand of matrix material, at 550 ℃, be incubated 4 hours and get rid of tackiness agent PVA, became porcelain in 0.5~2 hour, obtain the ferrous acid bismuth barium titanate sosoloid matrix material of high magnetic intensity and polarizability at 1000~1050 ℃ of following sintering.
2. the preparation method of the ferrous acid bismuth barium titanate sosoloid matrix material of high magnetic intensity according to claim 1 and polarizability is characterized in that: it is 5% polyvinyl alcohol water solution granulation after 60 orders and 120 eye mesh screens sieve makes that described PVA tackiness agent adopts mass concentration.
CN 201210023356 2012-02-02 2012-02-02 Preparation method of bismuth ferrate barium titanate solid solution composite material with high magnetization intensity and high polarization intensity Expired - Fee Related CN102584193B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 201210023356 CN102584193B (en) 2012-02-02 2012-02-02 Preparation method of bismuth ferrate barium titanate solid solution composite material with high magnetization intensity and high polarization intensity

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 201210023356 CN102584193B (en) 2012-02-02 2012-02-02 Preparation method of bismuth ferrate barium titanate solid solution composite material with high magnetization intensity and high polarization intensity

Publications (2)

Publication Number Publication Date
CN102584193A CN102584193A (en) 2012-07-18
CN102584193B true CN102584193B (en) 2013-07-24

Family

ID=46473533

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 201210023356 Expired - Fee Related CN102584193B (en) 2012-02-02 2012-02-02 Preparation method of bismuth ferrate barium titanate solid solution composite material with high magnetization intensity and high polarization intensity

Country Status (1)

Country Link
CN (1) CN102584193B (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104557028B (en) * 2015-01-14 2016-08-24 陕西科技大学 A kind of layered electromagnetic composite and preparation method thereof
CN104557029A (en) * 2015-01-14 2015-04-29 陕西科技大学 BiY2F25O12/BaTiO3 lamellar ferroelectric composite material as well as preparation method thereof
CN107417267B (en) * 2017-08-09 2020-01-03 歌尔股份有限公司 Bismuth ferrite multiferroic ceramic and preparation method thereof
CN109516796B (en) * 2018-11-30 2021-07-09 江西科技学院 Multiferroic solid solution ceramic and preparation method thereof
CN111253151B (en) * 2020-03-14 2022-05-17 杭州电子科技大学 Bismuth ferrite barium titanate-based ceramic with high energy storage density and high power density and preparation method thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4988648A (en) * 1985-11-29 1991-01-29 Okura Techno-Research Kabushiki Kaisha Homogeneous solid solution material and method of manufacturing the same
CN101255053A (en) * 2008-04-08 2008-09-03 同济大学 High-temperature single-phase ferromagnetic-ferroelectric multiferroics ceramic material and preparation method thereof
JP2010195639A (en) * 2009-02-26 2010-09-09 Murata Mfg Co Ltd Method of preparing ceramic slurry, method of manufacturing ceramic powder, ceramic powder, and method of forming ceramic green sheet
CN101913853A (en) * 2010-07-16 2010-12-15 北京科技大学 Method for preparing bismuth titanate-barium titanate powder by hydrothermal method
CN102173784A (en) * 2011-01-21 2011-09-07 天津大学 Method for preparing sodium bismuth titanate-barium titanate composite dielectric ceramic through sol cladding method

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4988648A (en) * 1985-11-29 1991-01-29 Okura Techno-Research Kabushiki Kaisha Homogeneous solid solution material and method of manufacturing the same
CN101255053A (en) * 2008-04-08 2008-09-03 同济大学 High-temperature single-phase ferromagnetic-ferroelectric multiferroics ceramic material and preparation method thereof
JP2010195639A (en) * 2009-02-26 2010-09-09 Murata Mfg Co Ltd Method of preparing ceramic slurry, method of manufacturing ceramic powder, ceramic powder, and method of forming ceramic green sheet
CN101913853A (en) * 2010-07-16 2010-12-15 北京科技大学 Method for preparing bismuth titanate-barium titanate powder by hydrothermal method
CN102173784A (en) * 2011-01-21 2011-09-07 天津大学 Method for preparing sodium bismuth titanate-barium titanate composite dielectric ceramic through sol cladding method

Also Published As

Publication number Publication date
CN102584193A (en) 2012-07-18

Similar Documents

Publication Publication Date Title
CN102584192B (en) Preparation method of bismuth ferrate barium titanate solid-solution-based composite material with high magnetization intensity and high resistivity
CN102503391B (en) Preparation method of bismuth ferrite-based composite material with high ferromagnetic and ferroelectric properties
Xi et al. Enhanced magnetic and conductive properties of Ba and Co co-doped BiFeO3 ceramics
Wei et al. Nonmagnetic Fe-site doping of BiFeO3 multiferroic ceramics
CN102584193B (en) Preparation method of bismuth ferrate barium titanate solid solution composite material with high magnetization intensity and high polarization intensity
Zhang et al. Dielectric, magnetic and magnetoelectric properties of Ni0. 5Zn0. 5Fe2O4+ Pb (Zr0. 48Ti0. 52) O3 composite ceramics
Miah et al. Synthesis and enhancement of multiferroic properties of (x) Ba0. 95Sr0. 05TiO3–(1− x) BiFe0. 90Dy0. 10O3 ceramics
Xu et al. The Study of Microstructure, Dielectric and Multiferroic Properties of (1− x) Co 0.8 Cu 0.2 Fe 2 O 4-x Ba 0.6 Sr 0.4 TiO 3 Composites
CN101255053B (en) High-temperature single-phase ferromagnetic-ferroelectric multiferroics ceramic material and preparation method thereof
Srinivas et al. Room temperature multiferroism and magnetoelectric coupling in BaTiO3–BaFe12O19 system
Li et al. Enhanced Multiferroic and Magnetocapacitive Properties of (1− x) Ba 0.7 Ca 0.3 TiO 3–x BiFeO 3 Ceramics
CN102850051B (en) YFeO3 base bi-phase magnetoelectricity composite material and preparation method thereof
Wang et al. Room temperature multiferroic properties of Fe-doped nonstoichiometric SrTiO3 ceramics at both A and B sites
Cheng et al. Effect of local structural distortion on magnetic and dielectric properties in BiFeO3 with Ba, Ti co-doping
CN102942361B (en) Ferrotianium cobalt acid bismuth stupalith of laminate structure and preparation method thereof
CN103030386B (en) Multiferroic ceramics with room-temperature highly ferromagnetic-ferroelectric and highly-magnetic dielectric effects and preparation method of multiferroic ceramics
Yao et al. The effects of magnetic field and polarization on the permeability and permittivity of (1–x) Ni0. 4Zn0. 6Fe2O4+ xPb (Zr0. 53Ti0. 47) O3 composites at high frequency
CN103724005B (en) A kind of holmium, manganese possessing room temperature multiferroic mixes bismuth ferrite pottery and preparation method thereof altogether
Qin et al. A comparative study on the dielectric and multiferroic properties of Co0. 5Zn0. 5Fe2O4/Ba0. 8Sr0. 2TiO3 composite ceramics
Min et al. Room-temperature multiferroic properties of Co-doped KNbO3 ceramics
CN107840659A (en) A kind of tungsten bronze pure phase room temperature multiferroic ceramics and preparation method thereof
Xu et al. Multiferroic properties of nanopowder-synthesized ferroelectric-ferromagnetic 0.6 BaTiO 3-0.4 NiFe 2 O 4 ceramic
Ding et al. Magnetization, Magnetoelectric Effect, and Structure Transition in $\hbox {BiFeO} _ {3} $ and $(\hbox {Bi} _ {0.95}\hbox {La} _ {0.05})\hbox {FeO} _ {3} $ Multiferroic Ceramics
Bai et al. The static and hyper-frequency magnetic properties of a ferromagnetic–ferroelectric composite
HUANG et al. Low temperature sintering behavior of La-Co substituted M-type strontium hexaferrites for use in microwave LTCC technology

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20130724

Termination date: 20160202

CF01 Termination of patent right due to non-payment of annual fee