CN1736951A - Preparation method of low permittivity nanometer microwave medium ceramic powder - Google Patents

Preparation method of low permittivity nanometer microwave medium ceramic powder Download PDF

Info

Publication number
CN1736951A
CN1736951A CN 200510050789 CN200510050789A CN1736951A CN 1736951 A CN1736951 A CN 1736951A CN 200510050789 CN200510050789 CN 200510050789 CN 200510050789 A CN200510050789 A CN 200510050789A CN 1736951 A CN1736951 A CN 1736951A
Authority
CN
China
Prior art keywords
magnesium
ceramic powder
citric acid
preparation
heating
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.)
Granted
Application number
CN 200510050789
Other languages
Chinese (zh)
Other versions
CN1300060C (en
Inventor
杨辉
张启龙
王焕平
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.)
Zhejiang University ZJU
Original Assignee
Zhejiang University ZJU
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 Zhejiang University ZJU filed Critical Zhejiang University ZJU
Priority to CNB2005100507892A priority Critical patent/CN1300060C/en
Publication of CN1736951A publication Critical patent/CN1736951A/en
Application granted granted Critical
Publication of CN1300060C publication Critical patent/CN1300060C/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Abstract

The invention discloses a preparation method for nano microwave medium ceramic powder of low dielectric constant, which comprises: (1) dissolving the magnesium into inorganic salt, and adding silicon sol to mix according to mole rate of 1:1; (2) adding an mount of citric acid into ethylene alcohol for heating dissolution; (3) mixing the said two solutions with given mole rate, heating to vaporize water; heating to 125-135Deg, keeping temperature for 2-4h; continuing to heating to 180-220Deg and keeping temperature for 2-4h; grinding the obtained black material and sintering at 800-1000Deg. This method decreases greatly the synthesis temperature. the product has excellent microwave dielectric property and well industrial application value.

Description

A kind of preparation method of low permittivity nanometer microwave medium ceramic powder
Technical field
The preparation method of a kind of low permittivity nanometer microwave medium ceramic powder of the present invention belongs to materials science field.
Background technology
Along with electronics develops to miniaturization, the miniaturization of the various electronic packages of inevitable requirement, microminiaturization.Components and parts miniaturization has at present obtained develop rapidly; Aspect laminated ceramic capacitor, 0603 has become main product, and 0402 has appeared on the market, and 0201 has succeeded in developing; The chip multilayer microwave device progressively replaces cavity configuration, and miniaturization day by day, has been reduced to 2.0 * 1.25 * 1.0 (mm as the size of the multilayer ceramic filter of Japanese village field company 3), from now on will be to being of a size of 1.0 * 0.8 * 0.6 (mm 3) even littler direction develop.
The key problem in technology that promotes device miniaturization, microminiaturization is the development of powder technology and thin film technique.With the laminated ceramic capacitor is example, the capacitor C=kS/h of dielectric ceramic, and the best approach that improves the dielectric ceramic electrical capacity is the thickness that reduces medium layer; And for microwave filter, resonant frequency f 0=1/2 π (LC) 1/2, under certain resonant frequency, electrical capacity is a definite value, for structure of reducing device and the dielectric loss that reduces material, should adopt low-k as far as possible, and reduces thickness of dielectric layers.The laminated ceramic capacitor film has been reduced to below the 5um at present, and generally between 20~300um, development trend from now on is ceramic condenser film and the following microwave device film of 10um of 1~5um to the thickness of multilayer ceramic filter.Film to be of five storeys at least above particle packing become the dielectric ceramic layer could guarantee effectively to isolate in electrode, the particulate size has determined the minimum thickness of medium layer, nano-powder is undoubtedly the best terms of settlement of the problems referred to above.The nanometer of powder granule is a great development direction of world's electronic ceramics, who have nanometer commodity technology who just will dominate market, each main manufacturer of the world all spends huge sums to nanoelectronic ceramic powder expansion research as AVX/Kyocera Corporation, Philips Components, TDK Corporation, Samsung EMCO, TAM Ceramics etc.
When medium ceramic material was applied to microwave circuit, material behavior and wiring figure can influence transmission signal, and the specific inductivity of medium ceramic material is big more, and the time of lag of line signal can be long more; Therefore, the medium ceramic material of exploitation low-k, significant to the circuit microelectronics under the high frequency.MgSiO 3, Mg 2SiO 4Deng MgO-SiO 2System's pottery has good microwave property, and its specific inductivity is low, quality factor is high; But owing to utilize conventional solid phase method could synthesizing MgSiO more than 1300 ℃ 3, Mg 2SiO 4Crystalline phase, and its sintering temperature is more than 1500 ℃, so relevant pure MgSiO 3, Mg 2SiO 4The research of crystalline phase pottery seldom.
Li Xiaotu etc. at " piezoelectricity and acousto-optic " 2004,26 (1) 48-51. " a kind of high frequency hangs down Jie MLC porcelain systematic research " literary composition to MgO-SiO 2-TiO 2System launches research, by adjusting Mg 2SiO 4With Mg 2TiO 4Ratio, obtain ε r=12 ± 35.058 (1GHz), tg δ<1 * 10 -4The low Jie's positive temperature coefficient ceramic material of high frequency that dielectric properties are good; Sun Jizhou etc. are at " XI AN JIAOTONG UNIVERSITY Subject Index " 2003,37 (6) 604-607. " MgO-SiO 2-TiO 2The research of system Co, Ca ion doping " studied Co, Ca to MgO-SiO 2-TiO 2The doping of system; Luo Linghong etc. have studied B in " Journal of Inorganic Materials " 2001,16 (5) 1009-1014. " high-frequency multilayer chip inductor dielectric material " 3O 3-P 2O 5-MgO-Al 2O 3-SiO 2The system devitrified glass is as the application of high-frequency multilayer chip inductor dielectric material.At MgO-SiO 2The superfine powder research aspect of system domesticly never sees that relevant report is arranged; Japan people such as Sei-ichi Suda at " Journal ofNon-Crystalline Solids " 1999,255178-184. " Synthesis of MgO-SiO 2AndCaO-SiO 2Amorphous powder by sol-gel process and ion exchange " in by in sol-gel process, carrying out ion-exchange, obtained the MgO-SiO of 0.3~0.4um 2Powder is with the MgO-SiO of this method preparation 2The granularity that is ceramic powder is bigger than normal, can not satisfy the requirement of ultrathin casting films of preparation and microdevice.
Summary of the invention
The present invention provides a kind of preparation method of dielectric constant microwave ceramic medium nano-powder from the requirement of microwave device miniaturization to microwave dielectric ceramic materials powder super-refinement, selects the good MgO-SiO of microwave property 2System is utilized the pechini method, and by bonding and the sterically hindered effect of ethylene glycol to metal ion, and the process heating and calcining decomposes organism and inorganic ion generation oxidizing reaction forms crystal grain, thereby obtains nano level MgO-SiO at a lower temperature 2Microwave dielectric ceramic powder.
The preparation method of a kind of low permittivity nanometer microwave medium ceramic powder that the present invention proposes may further comprise the steps:
(1) inorganic salt with magnesium are dissolved in the deionized water, are 1: 1 mol ratio adding silicon sol again by silicon and magnesium, fully stir to make it to mix;
(2) a certain amount of citric acid (CA) is joined in the ethylene glycol (EG), heating is dissolved citric acid in ethylene glycol, and the mol ratio of CA and EG is 1: 4~1: 8;
(3) be above-mentioned (1) to be mixed with the solution that makes of (2) in 1: 1~1: 4 by CA and the mol ratio of magnesium inorganic salt, stir; Slowly heating makes water evaporates; Be warmed up to 125 ℃~135 ℃ insulations 2~4 hours then, continue to be warmed up to 180 ℃~220 ℃ insulations 2~4 hours, obtain crisp atrament;
4. above-mentioned crisp atrament is ground, put into the high alumina crucible,, obtain white powder, be dielectric constant microwave ceramic medium nano-powder of the present invention 800 ℃~1000 ℃ calcinings.
The inorganic salt of described magnesium can be Mg (NO 3) 26H 2O, Mg (CH 3COOH) 24H 2O, MgCl 2
The present invention adopts Mg (NO 3) 26H 2O, Mg (CH 3COOH) 24H 2O, MgCl 2Inorganic salt and silicon sol in magnesium are raw material, and low price and raw material are easy to get; Utilize citric acid to bonding and the sterically hindered effect of the complexing action of metal ion, ethylene glycol, metal ion is evenly distributed in the polymkeric substance, thereby finally can obtains the compound of uniform ingredients metal ion.Adopt technology of the present invention, after 900 ℃ of calcinings, can obtain particle diameter at 80~100nm and finely disseminated MgSiO 3, Mg 2SiO 4The nano level microwave dielectric ceramic powder greatly reduces MgO-SiO 2The synthesis temperature of compound.The nano-powder that the present invention makes has excellent microwave dielectric properties (ε after sintering porcelain into r=6.4 ± 0.1, Qf>35000GHz), can be used for preparing small-sized chip multiplayer microwave devices such as 0402,0201 multiplayer microwave ceramic condenser has great industrial application value.
Embodiment
Below in conjunction with example the present invention is further described.
Embodiment 1:
Take by weighing the Mg (NO of 1mol 3) 26H 2O is dissolved in a certain amount of deionized water, forms the magnesium nitrate aqueous solution of 1mol/l; In this magnesium nitrate aqueous solution, be that the amount of 1mol adds silicon sol, stir it to be mixed in 3 hours by silicon.The citric acid (CA) of 1mol is joined in the ethylene glycol (EG) of 4mol, be heated to 90 ℃ citric acid is dissolved in ethylene glycol.
Above-mentioned two solution are mixed, stir, and slowly heating makes the water evaporates in the mixing solutions, obtains transparent colloidal sol shape liquid.The colloidal sol shape liquid that this is transparent is warmed up to 130 ℃ of insulations 3 hours, can produce bubble when beginning to be incubated and with volumetric expansion, insulation its volume of later stage no longer changes, and continues to be warmed up to 210 ℃ of insulations 2 hours, furnace cooling obtains crisp atrament then.
Above-mentioned crisp atrament is ground, put into the high alumina crucible,, obtain white powder, be nano material of the present invention 900 ℃ of calcinings 2 hours.
This material is through tem analysis, and particle diameter is between 80~100nm, and dispersion of particles is better; XRD analysis shows that this nano-powder is MgSiO 3, Mg 2SiO 4Mixed phase.
With the above-mentioned nanometer MgSiO that obtains 900 ℃ of calcinings 3, Mg 2SiO 4Grinding, granulation, be pressed into the nahlock of diameter 18mm height 8~9mm, at 1450 ℃ of sintering, its microwave dielectric property is: ε r=6.43, Qf=38900GHz.
Embodiment 2:
Take by weighing the MgCl of 1mol 2Be dissolved in a certain amount of deionized water, form the magnesium chloride brine of 0.8mol/l; In this magnesium chloride brine, be that the amount of 1mol adds silicon sol, stir it to be mixed in 4 hours by silicon.The citric acid (CA) of 2mol is joined in the ethylene glycol (EG) of 9mol, be heated to 90 ℃ citric acid is dissolved in ethylene glycol.
Above-mentioned two solution are mixed, stir, and slowly heating makes the water evaporates in the mixing solutions, obtains transparent colloidal sol shape liquid.The colloidal sol shape liquid that this is transparent is warmed up to 130 ℃ of insulations 3 hours, can produce bubble when beginning to be incubated and with volumetric expansion, insulation its volume of later stage no longer changes, and continues to be warmed up to 210 ℃ of insulations 2 hours, furnace cooling obtains crisp atrament then.
Above-mentioned crisp atrament is ground, put into the high alumina crucible,, obtain white powder, be nano material of the present invention 900 ℃ of calcinings 2 hours.
This material is through tem analysis, and particle diameter is between 80~95nm, and dispersion of particles is better; XRD analysis shows that this nano-powder is MgSiO 3, Mg 2SiO 4Mixed phase.
With the above-mentioned nanometer MgSiO that obtains 900 ℃ of calcinings 3, Mg 2SiO 4Grinding, granulation, be pressed into the nahlock of diameter 18mm height 8~9mm, at 1450 ℃ of sintering, its microwave dielectric property is: ε r=6.47, Qf=37000GHz.
Embodiment 3:
Take by weighing the Mg (CH of 1mol 3COOH) 24H 2O is dissolved in a certain amount of deionized water, forms the magnesium acetate aqueous solution of 1.5mol/l; In this magnesium acetate aqueous solution, be that the amount of 1mol adds silicon sol, stir it to be mixed in 4 hours by silicon.The citric acid (CA) of 1.5mol is joined in the ethylene glycol (EG) of 9mol, be heated to 90 ℃ citric acid is dissolved in ethylene glycol.
Above-mentioned two solution are mixed, stir, and slowly heating makes the water evaporates in the mixing solutions, obtains transparent colloidal sol shape liquid.The colloidal sol shape liquid that this is transparent is warmed up to 125 ℃ of insulations 4 hours, can produce bubble when beginning to be incubated and with volumetric expansion, insulation its volume of later stage no longer changes, and continues to be warmed up to 220 ℃ of insulations 3 hours, furnace cooling obtains crisp atrament then.
Above-mentioned crisp atrament is ground, put into the high alumina crucible,, obtain white powder, be nano material of the present invention 900 ℃ of calcinings 2 hours.
This material is through tem analysis, and particle diameter is between 80~100nm, and dispersion of particles is better; XRD analysis shows that this nano-powder is MgSiO 3, Mg 2SiO 4Mixed phase.
With the above-mentioned nanometer MgSiO that obtains 900 ℃ of calcinings 3, Mg 2SiO 4Grinding, granulation, be pressed into the nahlock of diameter 18mm height 8~9mm, at 1450 ℃ of sintering, its microwave dielectric property is: ε r=6.48, Qf=39500GHz.

Claims (2)

1, a kind of preparation method of low permittivity nanometer microwave medium ceramic powder may further comprise the steps:
(1) inorganic salt with magnesium are dissolved in the deionized water, form the inorganic salt solution of 0.5~1.5mol/l magnesium; Be 1: 1 mol ratio adding silicon sol again by silicon and magnesium, stirred 1~5 hour;
(2) a certain amount of citric acid is joined in the ethylene glycol, heating is dissolved citric acid in ethylene glycol, and the mol ratio of citric acid and ethylene glycol is 1: 4~1: 8;
(3) be above-mentioned (1) to be mixed with (2) solution in 1: 1~1: 4 by the citric acid and the mol ratio of magnesium inorganic salt, stir; Slowly heating makes water evaporates; Be warmed up to 125 ℃~135 ℃ insulations 2~4 hours then, continue to be warmed up to 180 ℃~220 ℃ insulations 2~4 hours, obtain crisp atrament;
(4) above-mentioned crisp atrament is ground, put into the high alumina crucible,, obtain white nano-ceramic powder 800 ℃~1000 ℃ calcinings.
2, the preparation method of low permittivity nanometer microwave medium ceramic powder according to claim 1 is characterized in that: the inorganic salt of described magnesium can be Mg (NO 3) 26H 2O, MgCl 2, Mg (CH 3COOH) 24H 2O.
CNB2005100507892A 2005-07-18 2005-07-18 Preparation method of low permittivity nanometer microwave medium ceramic powder Expired - Fee Related CN1300060C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB2005100507892A CN1300060C (en) 2005-07-18 2005-07-18 Preparation method of low permittivity nanometer microwave medium ceramic powder

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB2005100507892A CN1300060C (en) 2005-07-18 2005-07-18 Preparation method of low permittivity nanometer microwave medium ceramic powder

Publications (2)

Publication Number Publication Date
CN1736951A true CN1736951A (en) 2006-02-22
CN1300060C CN1300060C (en) 2007-02-14

Family

ID=36079938

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB2005100507892A Expired - Fee Related CN1300060C (en) 2005-07-18 2005-07-18 Preparation method of low permittivity nanometer microwave medium ceramic powder

Country Status (1)

Country Link
CN (1) CN1300060C (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103715408A (en) * 2013-12-13 2014-04-09 天津大学 Sol-gel preparation method of lithium zinc titanate as lithium ion battery cathode material
CN112194483A (en) * 2020-10-23 2021-01-08 厦门松元电子有限公司 High-strength calcium-magnesium-titanium microwave dielectric ceramic material and preparation method thereof

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1226229C (en) * 2003-06-30 2005-11-09 哈尔滨工业大学 Preparation method of composite silicate containing aluminium and/or magnesium

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103715408A (en) * 2013-12-13 2014-04-09 天津大学 Sol-gel preparation method of lithium zinc titanate as lithium ion battery cathode material
CN112194483A (en) * 2020-10-23 2021-01-08 厦门松元电子有限公司 High-strength calcium-magnesium-titanium microwave dielectric ceramic material and preparation method thereof

Also Published As

Publication number Publication date
CN1300060C (en) 2007-02-14

Similar Documents

Publication Publication Date Title
Yoon Tetragonality of barium titanate powder for a ceramic capacitor application
CN1903733A (en) Preparation method of single phase nano-CaTiO3 powder using collosol-gel low temperature synthesis
EP0584672A1 (en) Method of manufacturing an indium oxide powder useful as material of a high-density ITO sintered body
US6585951B1 (en) Methods for manufacturing dielectric powders
CN107033502A (en) Sour barium/organic matrix composite membrane of the neodymium-doped titanium of a kind of simple high energy storage density and preparation method thereof
Li et al. Effects of Ni2+ substitution on the crystal structure, bond valence, and microwave dielectric properties of BaAl2–2xNi2xSi2O8–x ceramics
CN104497357A (en) Hybrid particles and preparation method thereof as well as insulating compound material
CN1123551C (en) Nanometer grade tetragonal-phase barium titanate powder and its prepn.
CN1830775A (en) Method of preparing spherical nanometer SiO2 using powder quartz by chemical precipitation method
CN1300060C (en) Preparation method of low permittivity nanometer microwave medium ceramic powder
WO2019126969A1 (en) Dielectric ceramic material and method for preparing same
CN101538117A (en) Ferroelectric glass-ceramic dielectric material and preparation method thereof
CN100334034C (en) Method for low-temperature synthesis of nanometer CaO-SiO2 series nanometre microwave medium ceramic powder
Jin et al. Enhanced energy storage performance of lead-free BaTiO3-K0. 5Na0. 5NbO3 via grain engineering
CN101456561B (en) Method for preparing nano mullite powder
CN104445231B (en) A kind of silicate nano powder body with lower sintering temperature and preparation method thereof
CN102030525B (en) Low-temperature sintered magnesium titanate ceramic and preparation method thereof
CN1177776C (en) Silicate-based sintering acid and method
CN101928038B (en) Preparation method of barium titanate hollow nanospheres
CN101525151B (en) Manufacturing technique for high-purity electronic grade strontium titanate
Hao et al. Sol–gel based synthesis of ultrafine tetragonal BaTiO 3
Wang et al. A new strategy to realize phase structure and morphology of BaTiO3 nanowires controlled in ZnO-B2O3-SiO2 glass
CN1272280C (en) Preparation method of niobium doped barium sodium titanate nano-powder
Ma et al. Studies of phase transitions, Raman spectra and microwave dielectric properties of perovskite-structured (Na1− x Li x) 0.5 Nd0. 5TiO3 ceramics
CN102887705A (en) Preparation method of tetragonal-phase barium titanate (BaTiO3) hollow nanocrystal

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
C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20070214

Termination date: 20120718