EP2310338A2 - GRAINS FONDUS D'OXYDES COMPRENANT AL, TI et MG ET PRODUITS CERAMIQUES COMPORTANT DE TELS GRAINS - Google Patents

GRAINS FONDUS D'OXYDES COMPRENANT AL, TI et MG ET PRODUITS CERAMIQUES COMPORTANT DE TELS GRAINS

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Publication number
EP2310338A2
EP2310338A2 EP09772746A EP09772746A EP2310338A2 EP 2310338 A2 EP2310338 A2 EP 2310338A2 EP 09772746 A EP09772746 A EP 09772746A EP 09772746 A EP09772746 A EP 09772746A EP 2310338 A2 EP2310338 A2 EP 2310338A2
Authority
EP
European Patent Office
Prior art keywords
phase
less
grains
tio
oxides
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Withdrawn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
EP09772746A
Other languages
German (de)
English (en)
French (fr)
Inventor
Yves Boussant-Roux
Isabelle Cabodi
Samuel Marlin
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.)
Saint Gobain Centre de Recherche et dEtudes Europeen SAS
Original Assignee
Saint Gobain Centre de Recherche et dEtudes Europeen SAS
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 Saint Gobain Centre de Recherche et dEtudes Europeen SAS filed Critical Saint Gobain Centre de Recherche et dEtudes Europeen SAS
Publication of EP2310338A2 publication Critical patent/EP2310338A2/fr
Withdrawn legal-status Critical Current

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    • C04B35/01Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
    • C04B35/46Shaped 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
    • C04B35/462Shaped 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
    • C04B35/478Shaped 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 aluminium titanates
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D39/00Filtering material for liquid or gaseous fluids
    • B01D39/14Other self-supporting filtering material ; Other filtering material
    • B01D39/20Other self-supporting filtering material ; Other filtering material of inorganic material, e.g. asbestos paper, metallic filtering material of non-woven wires
    • B01D39/2068Other inorganic materials, e.g. ceramics
    • B01D39/2072Other inorganic materials, e.g. ceramics the material being particulate or granular
    • B01D39/2075Other inorganic materials, e.g. ceramics the material being particulate or granular sintered or bonded by inorganic agents
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    • B01J21/00Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/10Magnesium; Oxides or hydroxides thereof
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    • C04B2235/9669Resistance against chemicals, e.g. against molten glass or molten salts
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F01MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
    • F01NGAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
    • F01N3/00Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust
    • F01N3/02Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for cooling, or for removing solid constituents of, exhaust
    • F01N3/021Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for cooling, or for removing solid constituents of, exhaust by means of filters
    • F01N3/022Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for cooling, or for removing solid constituents of, exhaust by means of filters characterised by specially adapted filtering structure, e.g. honeycomb, mesh or fibrous
    • F01N3/0222Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for cooling, or for removing solid constituents of, exhaust by means of filters characterised by specially adapted filtering structure, e.g. honeycomb, mesh or fibrous the structure being monolithic, e.g. honeycombs
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F01MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
    • F01NGAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR MACHINES OR ENGINES IN GENERAL; GAS-FLOW SILENCERS OR EXHAUST APPARATUS FOR INTERNAL COMBUSTION ENGINES
    • F01N3/00Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust
    • F01N3/08Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous
    • F01N3/10Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous by thermal or catalytic conversion of noxious components of exhaust
    • F01N3/24Exhaust or silencing apparatus having means for purifying, rendering innocuous, or otherwise treating exhaust for rendering innocuous by thermal or catalytic conversion of noxious components of exhaust characterised by constructional aspects of converting apparatus
    • F01N3/28Construction of catalytic reactors
    • F01N3/2803Construction of catalytic reactors characterised by structure, by material or by manufacturing of catalyst support
    • F01N3/2825Ceramics
    • F01N3/2828Ceramic multi-channel monoliths, e.g. honeycombs
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/24Structurally defined web or sheet [e.g., overall dimension, etc.]
    • Y10T428/24149Honeycomb-like

Definitions

  • OXIDE-FILLED GRAINS COMPRISING AL, TI AND MG AND PRODUCTS
  • the invention relates to grains for ceramic applications consisting mainly of oxides of Mg, Al and Ti cations.
  • the invention also relates to a method of manufacturing such grains, as well as to ceramic products made from or comprising said grains, in particular but not only to filtering structures or catalytic supports, in particular used in an exhaust line of an internal combustion engine of the diesel type.
  • filtering structures or catalytic supports in particular used in an exhaust line of an internal combustion engine of the diesel type.
  • soot particles emitted by the engine are retained and are deposited inside the filter.
  • the soot particles are burned inside the filter, in order to restore its filtration properties. It is thus conceivable that the mechanical strength properties at both low and high temperature of the constituent material of the filter are essential for such an application. Similarly, the material must have a sufficiently stable structure to withstand, especially throughout the life of the equipped vehicle, temperatures that can locally rise to values that may be greater than 1000 0 C, especially if the phases of regenerations are poorly controlled.
  • the filters are mainly porous ceramic material, for example silicon carbide, cordierite, or aluminum titanate.
  • silicon carbide catalytic filters are for example described in patent applications EP 816 065,
  • a first disadvantage is related to the slightly high coefficient of thermal expansion of SiC, greater than 3.1CT 6 K -1 , which does not allow the production of monolithic filters of large size and usually requires the segmentation of the filter into several elements. in a honeycomb bonded by a cement, as described in application EP 1 455 923.
  • a second drawback, of economic nature is related to the extremely high firing temperature, typically greater than 2100 ° C., allowing a sintering ensuring a sufficient thermomechanical resistance of the honeycomb structures, in particular during the successive phases of regeneration of the filter Such temperatures require the installation of special equipment which significantly increases the cost of the filter finally obtained.
  • the cordierite filters are known and used for a long time, because of their low cost, it is now known that problems can occur in such structures, especially during poorly controlled regeneration cycles, during which the filter can be subjected locally to temperatures above the melting temperature of cordierite.
  • the consequences of these hot spots can range from a partial loss of efficiency of the filter to its total destruction in the most severe cases.
  • the cordierite does not have sufficient chemical inertia, with respect to the temperatures reached during successive cycles of regeneration and is therefore likely to react and be corroded by the species from residues of lubricant, fuel or other oils , accumulated in the structure during the filtration phases, this phenomenon can also be at the origin of the rapid deterioration of the properties of the structure.
  • such disadvantages are described in the patent application WO 2004/011124 which proposes to remedy a filter based on aluminum titanate (60 to 90% by weight), reinforced by mullite (10 to 40% by weight). ), whose durability is improved.
  • the application EP 1 559 696 proposes the use of powders for the manufacture of honeycomb filters obtained by reactive sintering of aluminum, titanium and magnesium oxides between 1000 and 1700 ° C. material obtained after sintering is in the form of a mixture of two phases: a majority phase of structural type pseudo-brookite or aluminum titanate Al 2 ⁇ 3.TiO 2 (Al 2 TiO 5 ) containing titanium, aluminum and magnesium and a minority feldspar phase, of the type
  • the object of the present invention is thus to provide new grains comprising or consisting of an oxide material of the pseudo-brookite type, having properties, as previously described, substantially improved, in particular so as to make it more advantageous for use in many areas of application of ceramic materials and in particular for the manufacture of a filtering structure and / or catalytic, typically honeycomb. More specifically, the present invention relates to molten grains mainly comprising or constituted by an oxide phase of the pseudo-brookite type and comprising titanium, aluminum and magnesium, said melted grains having the following chemical composition, in percentages by weight on the basis of oxides:
  • said melted grains additionally satisfying the following composition, in molar percentage and based solely on oxides Al 2 O 3 , TiO 2 , MgO:
  • m is the molar percentage of MgO.
  • phase of the pseudo-brookite type represents at least 60% and preferably at least 70% or even 80% of the total weight of the grains.
  • Al 2 O 3 represents more than 15% of the chemical composition, the percentages being given by weight on the basis of the oxides corresponding to the elements present in said grains.
  • Al 2 O 3 may represent more than 25% and more preferably more than 35% or even more than 39% of the chemical composition.
  • Al 2 O 3 represents less than 51% of the chemical composition, the percentages being given by weight on the basis of the oxides.
  • TiO 2 represents more than 35% and very preferably more than 39% of the chemical composition.
  • TiO 2 represents less than 60% and very preferably less than 55% of the chemical composition, the percentages being given by weight on the basis of the oxides.
  • MgO represents more than 1.5% and very preferably more than 2% of the chemical composition.
  • MgO represents less than 10% and very preferably less than 5% of the chemical composition, the percentages being given by weight and on the basis of the oxides.
  • the grains according to the invention may further comprise other minority elements.
  • the grains may comprise silicon, in an amount for example between 0.01 and 20%, preferably between 0.1 and 10%, on a SiO 2 base.
  • the grains may further comprise other elements such as Ca, Na, K, Fe, Zr, the total summed amount of said elements present being preferably less than 3% by weight, preferably less than 2% by weight based on the oxides. corresponding to the weight percentage of all the oxides present in said grains.
  • the weight percentage of each minor element, based on the weight of the oxide is preferably less than 0.7%.
  • the grains according to the invention may further comprise a minority phase constituted by a silicate phase, in proportions ranging from 0 to 40% of the total weight of the grains, preferably from 0 to 30% and very preferably from 0 to 25% of the total weight of the grains.
  • said silicate phase may consist mainly of silica and alumina.
  • the proportion of silica in the silicate phase is greater than 50%, or even greater than 60%.
  • the grains according to the invention may further comprise a minority phase essentially comprising TiO 2 titanium oxide. By the term "essentially comprising”, it is understood that the percentage weight TiO 2 in this phase is of the order of at least 80%, or even at least 90%.
  • the oxide phase of the pseudo-brookite type present in the melted grains is a solid solution that can respond substantially to the formulation
  • the invention also relates to ceramic products comprising grains as previously described, in particular for use in the following fields: manufacture of refractory parts used in contact with aluminum or molten metals, drawer plates, metal filters or manufacture of gazetterie for sintering furnaces.
  • the invention furthermore relates to ceramic products obtained after sintering of the preceding grains, at a temperature of between 1300 and 1800 ° C., said products being characterized in that they consist of a ceramic material comprising mainly or consisting of a oxide phase of the pseudo-brookite type and comprising titanium, aluminum and magnesium, in such proportions that the phase of the pseudo-brookite type substantially corresponds to the formulation (Al 2 TiOs) x (MgTi 2 O 5 ) IX , said material having the following chemical composition, in weight percent based on the oxides:
  • the value of x is not particularly limited and depends on the intended application and the desired properties for the grains.
  • the phase of the pseudo-brookite type of the ceramic material has the following chemical composition, in weight percentage on the basis of the oxides: - more than 39% and less than 54% of Al 2 ⁇ 3, for example more than 45% and less than 52% of Al 2 ⁇ 3, more than 45% and less than 55% of TiO 2 , for example less than 50% of TiO 2 , - more than 1% and less than 5% of MgO .
  • the ceramic product may comprise a main phase of the pseudo-brookite type and at least one secondary phase, said secondary phase being a silicate phase and / or a phase consisting essentially of TiO 2 titanium oxide.
  • the secondary phase is constituted by a silicate phase, in proportions ranging from 0 to 40% of the total weight of the material.
  • the preferred composition areas of the ceramic material are identical to those already described above in relation to the melted grains.
  • all possible combinations between the various preferred modes of the values and domains of compositions described. previously in relation to the composition of the grains are not repeated for the ceramic material but must be considered as included in the present description.
  • the grains of the invention can advantageously be prepared by electrofusion, which allows the production of large quantities of grains with attractive yields and a very good price / performance ratio.
  • the invention also relates to the process for producing previously described grains, comprising the following steps: a) mixing raw materials to form the feedstock; b) melting of the feedstock until the molten liquid is obtained; c) cooling said molten liquid so that the molten liquid is fully solidified, for example in less than 3 minutes; d) optionally, grinding said solid mass so as to obtain a mixture of grains.
  • the raw materials are chosen in step a) so that the grains obtained in step d) are in accordance with the invention.
  • any other conventional or known method of manufacturing molten grains may also be implemented, provided that the composition of the feedstock makes it possible to obtain grains having a composition in accordance with the invention. that of the grains of the invention.
  • an electric arc furnace is preferably used, but all the known furnaces are conceivable, such as an induction furnace or a plasma furnace, provided that they allow the charge to be completely melted. departure.
  • the firing is preferably carried out under neutral conditions, for example under argon, or oxidizing, preferably at atmospheric pressure.
  • the cooling can be rapid, that is to say that the molten liquid is fully solidified in less than 3 minutes.
  • the cooling can be rapid, that is to say that the molten liquid is fully solidified in less than 3 minutes.
  • it results from casting in CS molds as described in the patent
  • step d the solid mass is milled, according to conventional techniques, to obtain the grain size suitable for the intended application.
  • the present invention relates to a structure of the honeycomb type, made of a porous ceramic material, said structure consisting of a porous ceramic material obtained from at least 5% by weight of grains according to the invention and preferably at least 20%, 50%, 80% or even 100% by weight of grains according to the invention, said structure also having a porosity greater than 10% and a pore size centered between 5 and 60 microns.
  • the structures obtained according to the invention are intended for use as a particulate filter, they have a suitable porosity in general of between 20 and 65%, the average pore size being ideally between 10 and 20 microns.
  • Such filtering structures most often have a central part comprising a honeycomb filter element or a plurality of honeycomb filter elements interconnected by a joint cement, the one or more elements comprising a set of conduits. or adjacent channels of axes parallel to each other separated by porous walls, which conduits are closed by plugs at one or the other of their ends to delimiting inlet chambers s 'opening on a gas inlet face and outlet chambers s' opening on a gas evacuation face, so that the gas passes through the porous walls.
  • a method of manufacturing such a structure from an initial mixture of grains according to the invention is for example the following:
  • molten grains according to the invention are mixed as previously described.
  • the melted grains have been ground in such a way that they have a median diameter of less than 50 microns.
  • the manufacturing method typically comprises a step of mixing an initial mixture comprising the grains, an organic binder of the methylcellulose type and a porogen then adding water until the desired plasticity to allow the extrusion step following.
  • a mixture comprising: at least 5%, for example at least 50%, or even at least 90% or even 100% of grains according to the invention, the rest of the mixture being consist of powder or grains of other materials or even simple oxides of the elements Al, Ti, Mg or precursors of said oxides, for example in the form of carbonates, hydroxides or other organometallic compounds of the preceding elements,
  • the extrusion step of this product through a suitable die makes it possible to obtain monoliths in the form of a honeycomb.
  • the process comprises, for example, a drying step of the monoliths obtained.
  • the green ceramic monoliths obtained are typically dried by microwave or at a temperature for a time sufficient to bring the water content not chemically bound to less than 1% by weight.
  • the method may further comprise a plugging step of every other channel at each end of the monolith.
  • the firing step of the monoliths is carried out at a temperature greater than 1300 ° C. but not exceeding 1800 ° C., preferably not exceeding 1750 ° C.
  • the monolithic structure is brought to a temperature of temperature between 1400 0 C and 1600 0 C, under an atmosphere containing oxygen or a neutral gas.
  • the process may optionally comprise a step of assembling the monoliths in an assembled filtration structure according to well-known techniques, for example described in application EP 816 065.
  • the present invention also relates to a filter or a catalytic support obtained from of a structure as previously described and by deposition, preferably by impregnation, of at least one supported or preferably unsupported active catalytic phase, typically comprising at least one precious metal such as Pt and / or Rh and / or Pd and optionally an oxide such as CeO2, ZrO2, CeO2 ⁇ ZrO2.
  • Such structures find particular application as catalytic support in an exhaust line of a diesel engine or gasoline or particulate filter in an exhaust line of a diesel engine.
  • the samples were prepared from the following raw materials: Anathase containing more than 98% TiO 2 , marketed by Altichem or rutile with more than 95% TiO 2 and having a median diameter of 5%. o of about 120 microns, marketed by the company Europe Minerais, - Alumina AR75 comprising more than 98% of Al 2 O 3, sold by the company Alcan and having a median diameter of 5 o of about 85 microns,
  • MgO with a degree of purity higher than 98% with more than 80% of particles having a diameter of between 0.25 and 1 mm, marketed by the company Nedmag, - lime comprising approximately 97% of CaO, with more than 80% particles having a diameter of less than 80 ⁇ m,
  • the samples of Examples 1, 2, 4 and 5 according to the invention were obtained by melting the mixture of the preceding powders, in the appropriate proportions.
  • the initial reagent mixtures were blown in an electric arc furnace under air.
  • the molten mixture was then cast into a CS mold so as to obtain rapid cooling.
  • the product obtained is crushed and sieved to retain the powder passing at 36 microns.
  • This powder is used to make pressed samples with a diameter of 35 mm which are then sintered at a temperature of 1450 ° C. for 4 hours.
  • Example 3 an electron microprobe analysis of the sample according to example 4 is shown. Black porosities 1 are observed, in dark gray a majority phase 2 comprising titanium, aluminum and magnesium in the form of from a solid solution of an oxide and in light gray a second phase 3 consisting mainly of TiO 2. There is also the absence of silicate phase.
  • the initial oxides were directly mixed in the same proportions as for Example 2 according to the invention.
  • the raw materials of Example 2 were premixed in the same proportions and then sintered at 1450 ° C. for 4 hours. The product thus obtained was then milled and then sintered and sintered at 1450 ° C. for 4 hours.
  • the sample finally obtained according to Example 3 is not in accordance with the invention and given only for comparison.
  • AMTx indicates a solid solution of the type
  • the stability of the crystalline phases present is evaluated by a test consisting in comparing by diffraction of the RX the crystalline phases present initially to those present after a thermal treatment of 10 or 100 hours at 1100 0 C. If the phases remain identical after this treatment, the product is considered to be stable.
  • the coefficient of thermal expansion corresponds classically to the average of the values obtained from 25 ° C. to 1000 ° C. by dilatometry on pellets prepared from powders of the same granulometric slice, whose median diameter d 5 o is less than 50 ⁇ m.
  • the pellets are obtained by pressing and then sintering at 1450 ° C. for 3 hours in air.
  • the resistance to corrosion is evaluated by putting a sample of powder pressed and sintered, in the form of a disc of diameter 35 mm, in the presence of K 2 SO 4 . 0.2 grams of K 2 SO 4 powder are uniformly deposited on the surface of the disc. The sample as well covered is then brought to 1300 0 C under air for 5 hours. After cooling, the sample is cut in a radial section and prepared for sectional observation with a Scanning Electron Microscope. The depth E of the sample, from the initial surface of the disk affected by the corrosion, is then visually evaluated on the SEM photographs.
  • the modulus of rupture is determined at room temperature in 4-point bending conventionally on bars of dimensions 45 mm ⁇ 4 mm ⁇ 3 mm.
  • Table 1 It can be seen by comparing the data in Table 1 that the grains according to the invention make it possible finally to obtain ceramic products characterized by both good thermal stability, sufficient mechanical strength and improved corrosion resistance. very strongly, as the comparison of the eroded depths of the samples of Examples 2 and 3 shows.
  • each phase was then analyzed by microprobe analysis, the results of the analysis being given in Table 2. On the basis of these results, the weight percentage of each phase as well as the value of x in the formula (Al 2 TiOs) x (MgTi 2 O 5 ) IX of the main phase AMTx could be estimated by calculation.
  • Example 6 To study the characteristics of shaped parts of the material obtained according to the invention, particularly for As an application as particle filters, samples were prepared from the melted grains according to the invention and prepared according to Example 1 and a mixture of raw materials (new Example 6). In Example 6, commercially available powders were used as simple oxides of aluminum, silicon, magnesium and titanium.
  • median diameter refers to the diameter of the particles below which 50% by volume of the population is located.
  • a porous ceramic material is obtained in the following manner: the powders (melted grains for example 1 and simple oxides for example 6) are mixed with 5%, relative to the total weight of the mixture of powders, an organic binder of the methylcellulose type and 8% of a pore-forming agent. Water is added by mixing to obtain a homogeneous paste and whose plasticity allows the extrusion of a sample in the form of a bar size 6 mm x 8 mm x 60 mm, which is then sintered to 1450 0 C for 4 hours. On these samples, in order to estimate the value of the material used in a "particle filter" application, the coefficient of thermal expansion, the modulus of rupture as well as porosity characteristics are measured. Conventionally, these characteristics are measured by the well-known high-pressure mercury porosimetry techniques using a Micromeritics 9500 porosimeter.
  • the sintering shrinkage expresses the dimensional variation of the sample after sintering at 1450 ° C. More precisely, according to the invention, the term "shrinkage" is used. sintering the average decrease in each of the two dimensions of the section of the material, persistent at low temperature, that is to say at a temperature below 400 0 C and in particular at ambient. In Table 3, the reported value of the withdrawal corresponds to the average of the shrinkage for the two dimensions, expressed as a percentage of the initial dimension of the bar before sintering, for each of said dimensions. This feature is extremely important for estimating the feasibility of the porous structure manufacturing process.
  • the modulus of rupture (MOR) is determined at room temperature in 3-point bending on porous strips of size 6 mm ⁇ 8 mm ⁇ 60 mm obtained previously. The results are shown in Table 3.
  • Example 5 The material obtained according to Example 5 has a mechanical strength MOR very slightly lower than that obtained for Examples 1 and 6, but characteristics and properties of porosity, sintering shrinkage and coefficient of thermal expansion substantially improved.
  • the invention also relates to the use of the grains of the invention in other applications, especially all those where good thermal stability and a good CTE are required.
  • the size of the melted grains according to the invention may in particular be adapted, in particular by choosing a suitable grinding mode.

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EP09772746A 2008-07-04 2009-07-02 GRAINS FONDUS D'OXYDES COMPRENANT AL, TI et MG ET PRODUITS CERAMIQUES COMPORTANT DE TELS GRAINS Withdrawn EP2310338A2 (fr)

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PCT/FR2009/051294 WO2010001064A2 (fr) 2008-07-04 2009-07-02 GRAINS FONDUS D'OXYDES COMPRENANT AL, TI et MG ET PRODUITS CERAMIQUES COMPORTANT DE TELS GRAINS

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EP2221287B1 (en) * 2007-11-14 2015-06-03 Hitachi Metals, Ltd. Aluminum titanate based ceramic honeycomb structure, process for production of the same and raw material powder for the production thereof
US9623360B2 (en) 2013-05-20 2017-04-18 Corning Incorporated Porous ceramic article and method of manufacturing the same
US9376347B2 (en) 2013-05-20 2016-06-28 Corning Incorporated Porous ceramic article and method of manufacturing the same
US9908260B2 (en) 2013-05-20 2018-03-06 Corning Incorporated Porous ceramic article and method of manufacturing the same
MX2018014812A (es) 2016-05-31 2019-03-14 Corning Inc Articulo poroso y metodo para la fabricacion del mismo.
SI3475378T1 (sl) 2016-06-28 2020-12-31 Showa Denko K.K., Elektrotaljena zrna aluminijevega oksida, proizvodni postopek za elektrotaljena zrna aluminijevega oksida, brusilni kamen in oplaščen abraziv
CN111527054B (zh) 2017-10-31 2023-09-01 康宁股份有限公司 包含球形预反应过的无机颗粒和球形造孔剂的批料组合物及由其制造蜂窝体的方法

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WO2010001064A3 (fr) 2010-11-25
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US8715807B2 (en) 2014-05-06

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