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EP1529022A2 - Ceramiques haute densite et procede de fabrication associe - Google Patents

Ceramiques haute densite et procede de fabrication associe

Info

Publication number
EP1529022A2
EP1529022A2 EP03790724A EP03790724A EP1529022A2 EP 1529022 A2 EP1529022 A2 EP 1529022A2 EP 03790724 A EP03790724 A EP 03790724A EP 03790724 A EP03790724 A EP 03790724A EP 1529022 A2 EP1529022 A2 EP 1529022A2
Authority
EP
European Patent Office
Prior art keywords
density
produced
ceramics
starting powder
ceramic
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.)
Withdrawn
Application number
EP03790724A
Other languages
German (de)
English (en)
Inventor
Christian Pithan
Rainer Waser
Franz-Hubert Haegel
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.)
Forschungszentrum Juelich GmbH
Original Assignee
Forschungszentrum Juelich GmbH
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 Forschungszentrum Juelich GmbH filed Critical Forschungszentrum Juelich GmbH
Publication of EP1529022A2 publication Critical patent/EP1529022A2/fr
Withdrawn legal-status Critical Current

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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
    • C04B35/64—Burning or sintering processes
    • C04B35/645—Pressure sintering
    • C04B35/6455—Hot isostatic pressing
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
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    • C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B13/00—Oxygen; Ozone; Oxides or hydroxides in general
    • C01B13/14—Methods for preparing oxides or hydroxides in general
    • C01B13/32—Methods for preparing oxides or hydroxides in general by oxidation or hydrolysis of elements or compounds in the liquid or solid state or in non-aqueous solution, e.g. sol-gel process
    • C01B13/328—Methods for preparing oxides or hydroxides in general by oxidation or hydrolysis of elements or compounds in the liquid or solid state or in non-aqueous solution, e.g. sol-gel process by processes making use of emulsions, e.g. the kerosine process
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    • C01B13/14—Methods for preparing oxides or hydroxides in general
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    • C01G23/006—Alkaline earth titanates
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    • 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
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    • 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
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    • C04B35/4682—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 based on BaTiO3 perovskite phase
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Definitions

  • the invention relates to ceramics, in particular high-density ceramics with advantageous mechanical, dielectric, piezoelectric or magnetic properties.
  • the invention further relates to a method for producing these ceramics, in particular a method for producing oxidic nanoparticles as the starting substance for the high-density ceramics.
  • the so-called functional ceramics are used due to different material properties. These include, for example, temperature-dependent electron (insulators, semiconductors, superconductors) or ion conduction (sensors, membranes, fuel cells), magnetism (permanent magnets, data storage), dielectric, piezo or pyroelectric behavior and catalytic activity.
  • the area of application of the functional ceramics is therefore to be found preferably in the field of microelectronics (insulators, semiconductors, sensors, actuators) and conventional electronics (resistors, capacitors, thermistors and varistors), as well as electrical engineering (HT heating conductors).
  • the number of suitable materials as functional ceramics is constantly increasing. The relevant material properties of these ceramics are causally related to the atomic structure, especially the crystal structure.
  • the barium titanate that is tetragonal at room temperature and crystallized in a perovskite structure forms a ferro- and piezoelectric phase. If the Curie temperature is exceeded, a change of modification to a cubic, paraelectric structure takes place. The shift in atomic positions associated with the tetragonal structure leads to the formation of a permanent dipole moment and thus to a high dielectric constant.
  • the Curie temperature can be set by targeted doping, above which there is also a strong change in the specific resistance.
  • the properties of the finished ceramic depend to a large extent on the phase composition of the solid, the crystal size and the porosity. Ceramics are manufactured from an inhomogeneous material Mix of solid raw materials below the melting point. Therefore, transport processes and diffusion paths of the ions or atoms are of crucial importance for the formation of homogeneous and high-density ceramics.
  • the improved mechanical stability of ceramics made of nanoparticles is based on an improved homogeneity and a controlled particle size distribution in the green bodies.
  • the production of only weakly agglomerated starting powders leads to the production of dense, uniform and fine-grained ceramic microstructures, which have a significantly reduced sintering temperature, via also only weakly agglomerated ceramic powders.
  • Studies on the production of non-agglomerated, ultrafine powders for the systems yttrium, titanium and yttrium-stabilized zirconium oxide from [1] are known. Examination of the starting powders in a scanning electron microscope reveals an average particle size of approximately 20 nm for the titanium dioxide and 10 to 20 nm for the yttrium-stabilized zirconium oxide.
  • the particles had mean sizes of 3.0 to 15.9 nm for different compositions of the microemulsion.
  • the width of the particle size distribution ⁇ was 1.1 to 1.9 nm.
  • the worst case the smallest particles with 3.0 nm correspond to a share of ⁇ 5% for particles with a diameter greater than 9.0 nm, the Three times the mean. The corresponding proportions are much lower for the larger particles.
  • the hot pressing and sinter forging of materials with particles ⁇ 10 nm is e.g. B. from Kear, Chag, Skandan and Hahn in US 5,514,350.
  • the particle separation takes place from the gas phase and therefore only achieves low particle concentrations.
  • the particle size distribution is also wider than for microemulsion synthesis. Not all materials can be easily separated with the correct stoichiometry via the gas phase.
  • the pressure-assisted consolidation of loosely aggregated ceramic nanopowders with a metastable structure is described by Kear, Liao and Mayo in US Pat. No. 6,395,214.
  • the pressures used are very high. They are 3-5.5 GPa.
  • the temperature is given as 0.2 to 0.6 times the absolute melting temperature.
  • the powders used have small particles of 10-20 nm, but no narrow particle size distribution (FIG. 2 of the cited patent).
  • Ceramics are mainly used in the fields of electronics, optics, mechanical engineering and medicine. In the field of electro-ceramic materials, ceramics with magnetic, ferroelectric, dielectric, piezoelectric, pyroelectric, photoelectrochemical, semiconducting, ion-conducting, superconducting, electro-optical properties have a wide variety of applications.
  • Ferroelectrics exhibit a structural phase transition from a low-temperature ferroelectric phase to a high-temperature paraelectric phase, which is generally associated with a very strong dependence of the dielectric constants of the material on the temperature.
  • T c Curie temperature
  • both the dielectric and the piezoelectric coefficients have maximum values which drop drastically for both lower and higher temperatures.
  • Such a pronounced temperature behavior is indispensable in many technological applications. wishes, because in the use of the material a possible warming caused by the operation affects the change of the characteristic values of the corresponding component. It is known that the grain size of electroceramic materials has a very strong effect on the ferroelectric phase transition. As a rule, the destabilization of ferrodelect-
  • the object of the invention is to create high-density ceramics with particularly advantageous properties with regard to strength, density and mechanical, dielectric, piezoelectric or magnetic properties. Furthermore, it is the task of the invention to provide a production method for this type of ceramic with the corresponding ceramic starting powder in the form of nanoparticles.
  • the objects of the invention are achieved by a production method for a high-density ceramic made of nanoparticles with all the features of the main claim, and by high-density ceramics with all the features of the secondary claim. Further advantageous refinements of the method and the ceramic can be found in the claims which refer back to them.
  • the invention relates to a method for producing high-density ceramics from nanoparticles, and materials in the form of nanoparticles and high-density ceramics.
  • the process produces oxidic nanoparticles by hydrolysing water-sensitive compounds with microemulsions.
  • the particles of the desired stoichiometric composition generated in this way can already be used with the aid of pressure-assisted processes very low temperatures can be processed into high-density ceramics.
  • the ceramics are supported by pressure-supported consolidation, e.g. B. by gas pressure sintering, hot pressing or sintering from powders, the
  • Primary particles have an average size ⁇ 100 nm, preferably ⁇ 50 nm and particularly preferably ⁇ 10 nm.
  • the primary particles are by hydrolysis of alkoxides or a mixture of alkoxides and other easily hydrolyzable compounds, such as. B. halides, oxalates or acetates, with microemulsions.
  • the compound to be hydrolyzed or the compounds to be hydrolyzed are initially introduced, at least in part, in a solvent which can be miscible or immiscible with water and hydrolyzed by adding a microemulsion. This produces oxide or hydroxide or mixed oxide-hydroxide nanoparticles with a very narrow size distribution, with less than 10%, preferably less than 5% and particularly preferably less than 2% of the particles
  • This microemulsion contains at least the three components, water, a water-immiscible solvent and a surfactant.
  • Technical surfactants are usually already multi-component mixtures.
  • other components can be added, such as. B. alcohols as cosurfactants or one or more of the reactants or buffers.
  • the surfactants can be non-ionic, anionic or cationic.
  • Nonionic surfactants are preferably used, since they can be removed without residue by thermal decomposition.
  • the synthesis is not limited to the elements and compounds mentioned. In principle, any hydrolyzable compound which forms the corresponding oxide, hydroxide or an oxide hydroxide is suitable.
  • the oxides can be obtained from hydroxides and oxide hydroxides by calcining.
  • a stoichiometric compound such as. B. in the case of BaTi0 3 , where the stoichiometric 1: 1 composite mixed barium titanium iso-propoxide is formed, which is then hydrolyzed with a microemulsion.
  • the stoichiometric composition of the oxides can be set very precisely and easily if parts of the compound or of the product do not decompose during and after the formation of the particles.
  • the reduction in the polarity of the solvent in the reaction mixture which is brought about by the addition of the apolar phase of the microemulsion or by the use of a nonpolar solvent for the substance to be hydrolyzed, suppresses the decomposition of the product, as is particularly good in alcohol or Excess water soluble components of mixed oxides, hydroxides or oxide hydroxides can occur.
  • the solubility of the alkali ions in the form of their hydroxides can thus be greatly reduced and the preservation of the stoichiometry can be guaranteed regularly.
  • the oxides can be obtained in crystalline form during the synthesis. However, it is particularly advantageous for the subsequent compression to use the oxides in amorphous form. In order to keep the particles in amorphous form, it is necessary to increase the hydrolysis rate. This can be achieved, for example, by using particularly reactive hydrolyzable compounds, increasing the polarity of the water-immiscible solvent used for the microemulsion, by a high water content of the microemulsion, by increasing the temperature or by several of the measures mentioned.
  • the materials produced during the hydrolysis are then isolated and cleaned.
  • the powders obtained generally consist of loose agglomerates of the primary particles. If necessary, they can first be freed of organic components by heating to over 500 ° C and then by a process for pressure-assisted consolidation, e.g. B. by gas pressure sintering, hot pressing or sinter forging at comparatively low temperatures and pressures to high-density ceramics. If the organic constituents can be largely separated off during cleaning, direct compression using pressure-assisted processes is also possible.
  • the surfactant from the manufacturing process itself if appropriate after reducing the surfactant content in the raw powder by extraction with an organic solvent, can be a suitable binder for compacting the powder to form the green body.
  • surfactants of the alkyl polyethoxylate type have proven to be advantageous over alkyl aryl ethoxylates.
  • the temperature required for compression drops considerably with decreasing particle size. It is therefore advantageous to use particles ⁇ 100 nm, preferably ⁇ 50 nm and particularly preferably ⁇ 10 nm.
  • the temperature required for the compression can be further reduced if the particles are in amorphous form. Even at comparatively low temperatures, this enables gentle conditions, the pressure-free production of dense ceramics with densities> 90%, preferably> 95%.
  • the ceramics that can be produced by the combination of microemulsion synthesis and pressure-supported consolidation have particularly favorable properties, since they have a small average grain size and a uniform grain size distribution at high density.
  • the densities are greater than or equal to 94%, preferably> 97%, particularly preferably> 99%.
  • the mean grain size is ⁇ 500 nm, preferably ⁇ 100 nm and particularly preferably ⁇ 50 nm.
  • the ceramics also have a narrow grain size distribution, the proportion of grains with more than three times the mean grain size advantageously ⁇ 20% and in particular ⁇ 10 % is.
  • Ceramics that are produced in accordance with the method according to the invention have a through the Grain size-controlled temperature characteristics of the dielectric material properties additionally have smaller leakage currents, since the grain sizes grow only slightly during the sintering process and the proportion of electrically blocking grain boundaries thus remains high.
  • KNaNb 2 0 6 is a particularly advantageous piezoelectric material that has only a slightly smaller piezoelectric effect than that of Pb (Ti, Zr) 0 3 used in many areas.
  • Pb Ti, Zr
  • Potassium sodium niobates could be an interesting biocompatible and toxicologically harmless alternative material.
  • the compression of ceramic powders into compact ceramics is problematic. Due to the very low sintering activity, only very low relative densities below 94% can be set in conventional KNaNb 2 0 6 powders even at a temperature of 1100 ° C. A significant improvement in the sintering activity occurs in the ceramics which have been produced by the process according to the invention.
  • high-density ceramics Due to the fineness of the starting powder and the use of pressure-supported consolidation, high-density ceramics can be achieved at a temperature of 1050 ° C and a pressure of 19 MPa.
  • the ceramics obtained are translucent and thus almost have the theoretical density.
  • the uniformity of the particles has a particularly advantageous effect. because, despite the faster growth processes, the uniformity of the grains is largely retained and the grain growth is even.
  • Fig. 1 Nanocrystalline BaTi0 3 powder from microemulsion synthesis consisting of loosely aggregated primary particles (scanning electron microscope image).
  • Fig. 2 Nanocrystalline BaTi0 3 powder from microemulsion synthesis annealed at 800 ° C for one hour (scanning electron microscope image). Because of the uniformity of the primary particles, the growth rate of the grains is uniform during the sintering process.
  • A. Nanoparticle synthesis Al Synthesis of crystalline BaTi0 3 using a microemulsion with an alkylaryl polyethoxylate Crystalline (pseudocubic) BaTi0 3 was prepared according to the procedure in [4]. For this, barium was dissolved in 2-propanol. After the stoichiometric amount of titanium tetra-iso-propoxide was added, the mixture was stirred for one hour. A microemulsion of cyclohexane, Tergitol NP 35, octanol and the stoichiometric amount of water was then added to the reaction mixture. The particles were isolated and purified by removing the solvent, boiling with acetone, filtration and Soxhlet extraction.
  • A.2 Synthesis of crystalline BaTi0 3 using a microemulsion with an alkyl polyethoxylate
  • the synthesis was carried out in accordance with Al.
  • the microemulsion used contained the components cyclohexane, Lutensol ON 110 (from BASF), octanol and water.
  • Amorphous BaTi0 3 was obtained when a microemulsion for the hydrolysis of the mixed barium-titanium-iso-propoxide was used with a polar oil.
  • the composition of the microemulsion was Tergitol TMN 6 (Fluka) 4.970 g ethyl butyrate (Fluka) 12.456 g water 2.601 g
  • the X-ray diffraction diagrams show that the barium titanate is largely phase-pure.
  • the material contained small amounts of BaC0 3 . 0.2% inorganic carbon was found in the raw powder.
  • the content of inorganic carbon increases to a maximum of 0.7% due to the oxidation of the organic components of the raw powder.
  • the proportion is reduced to 0.05%.
  • the peaks for the raw powder from the microemulsion synthesis are greatly broadened because of the small particle size (FIG. 3a).
  • ceramics with different particle sizes can be produced. With increasing sintering temperature, the grains grow and the peaks become narrower (Fig. 3b).
  • the X-ray diffraction diagram of the potassium sodium niobate shows no foreign phases despite the addition of a stoichiometric amount of water after sintering of the amorphous material than at 1000 ° C. (FIG. 4).
  • FIG. 5 shows the comparison of the sintering curves for BaTi0 3 nanoparticles of 10 nm from the microemulsion synthesis according to 1.1. and two commercial powders with particle sizes of 50-70 nm or 2 ⁇ m. The data show that the powder from microemulsion synthesis in the range of 900-1150 ° C already achieves higher densities at lower temperatures than the comparison powder.
  • the surfactant content of the raw powder was reduced by boiling in acetone. The surfactant was largely removed. The total carbon content was still
  • a first compression step the powder was pressed with the surfactant as a binder in a steel matrix under 20 kN. (130 MPa) to a green body of 40 - 45% of the theoretical density.
  • the subsequent first tempering step up to 400 ° C the total carbon content was reduced to 1.23 + 0.04%.
  • the pressing was then cold isostatically compressed to a density of 55-60% at 550 MPa.
  • the presence of residues of organic carbon proved to be beneficial, since premature agglomeration of the particles was suppressed.
  • the remaining binder was burned out in air at 650 ° C.
  • the finished sintered body In order to obtain a maximum density of the finished sintered body, it was welded into a noble metal capsule.
  • the capsule with the pressing was first cold isostatically pressed at 400 MPa in order to ensure that the metal was pressed tightly against the pressing.
  • the sample was sintered at 850 ° C and 200 MPa for 15 minutes. It became a ceramic with a density of 98 ⁇ 0.6% of the theoretical density and an average grain size of 50.4 nm were obtained.
  • Ceramics which can be prepared with the inventions to the invention method, the ceramics Ba 3 and Ti0 KNaNb 2 0 6 described in the embodiments, but also BaFe 12 0 ⁇ 9
  • Both oxides belong to the class of ferroelectrics. They have a structural phase transition from a ferro-electrical low-temperature phase to a paraelectric high-temperature phase, which is generally associated with a very strong dependence of the dielectric constants of the material on the temperature.
  • T Curie temperature

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Abstract

L'invention concerne un procédé pour fabriquer des céramiques haute densité, selon lequel des nanoparticules d'oxyde sont d'abord produites par hydrolyse de composés sensibles à l'eau avec des microémulsions. Les particules ainsi obtenues, de proportions stoechiométriques données, sont façonnées en des céramiques haute densité par un procédé faisant appel à la pression à des températures très basses. La fine répartition dimensionnelle des particules permet de réaliser des céramiques à distribution granulométrique serrée à partir des poudres de départ à base de microémulsions. L'uniformité des particules primaires régularise la vitesse de croissance des grains pendant le frittage. Les céramiques fabriquées selon le procédé de l'invention présentent en outre des courants de fuite moindres pour une caractéristique des températures des propriétés diélectriques du matériau établie sur la base de la grosseur des grains. En effet, la grosseur des grains augmente peu lors du frittage, la part des joints de grain à blocage électrique restant ainsi élevée.
EP03790724A 2002-08-14 2003-08-14 Ceramiques haute densite et procede de fabrication associe Withdrawn EP1529022A2 (fr)

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DE102005040582A1 (de) * 2005-08-22 2007-03-01 Itn Nanovation Gmbh Hochtemperaturstabile keramische Schichten und Formkörper
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US5514350A (en) * 1994-04-22 1996-05-07 Rutgers, The State University Of New Jersey Apparatus for making nanostructured ceramic powders and whiskers
IT1270200B (it) * 1994-06-09 1997-04-29 Ausimont Spa Preparazione di particelle ultra fini da microemulsioni di acqua in olio
DE4444597C2 (de) * 1994-12-14 1998-11-05 Klingspor Gmbh C Verfahren zur Herstellung eines Aluminiumoxid enthaltenden gesinterten Materials
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US6395214B1 (en) * 1998-11-30 2002-05-28 Rutgers, The State University Of New Jersey High pressure and low temperature sintering of nanophase ceramic powders

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