GB2168337A - Ceramic foam - Google Patents
Ceramic foam Download PDFInfo
- Publication number
- GB2168337A GB2168337A GB08527212A GB8527212A GB2168337A GB 2168337 A GB2168337 A GB 2168337A GB 08527212 A GB08527212 A GB 08527212A GB 8527212 A GB8527212 A GB 8527212A GB 2168337 A GB2168337 A GB 2168337A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ceramic
- strands
- ceramic foam
- foam
- micrometers
- 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
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D39/00—Filtering material for liquid or gaseous fluids
- B01D39/14—Other self-supporting filtering material ; Other filtering material
- B01D39/20—Other self-supporting filtering material ; Other filtering material of inorganic material, e.g. asbestos paper, metallic filtering material of non-woven wires
- B01D39/2068—Other inorganic materials, e.g. ceramics
- B01D39/2093—Ceramic foam
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B38/00—Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof
- C04B38/06—Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof by burning-out added substances by burning natural expanding materials or by sublimating or melting out added substances
- C04B38/0615—Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof by burning-out added substances by burning natural expanding materials or by sublimating or melting out added substances the burned-out substance being a monolitic element having approximately the same dimensions as the final article, e.g. a porous polyurethane sheet or a prepreg obtained by bonding together resin particles
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Inorganic Chemistry (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Geology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Porous Artificial Stone Or Porous Ceramic Products (AREA)
- Filtering Materials (AREA)
- Catalysts (AREA)
- Glass Compositions (AREA)
Abstract
A ceramic foam has a three-dimensionally reticulated ceramic structure in that a bulk density thereof is between 0.4 and 2.0. An apparent porosity of many ceramic strands is 5% or less. Each of the strands has plural ceramic layers. A method for manufacturing a ceramic foam includes the steps of impregnating a basic urethane foam having a three-dimensionally reticulated structure with a slurry or slip for ceramic manufacturing purpose, drying them plural times so as to increase a thickness of the ceramic strands, and firing them thereby to obtain a ceramic body.
Description
SPECIFICATION
A ceramic foam and a method for making the same
This invention relates to a ceramic foam having a three-dimensionally reticulated ceramic structure which can be used as a filter for removing slugs contained in a molten metal, a heater for a burner or the like, and a method for manufacturing the same.
In order to remove slugs and other obstacles contained in a molten metal, a ceramic foam filter is used. The conventional ceramic foams used as a filter are made of cordierite, alumina or silicon carbide and have a void ratio of 75-95%, a bulk density of 0.2-03, an apparent porosity of interconnected ceramic strands ranging from 10% to 20%.
In a conventional ceramic foam, a soft urethane foam having a three-dimensionally reticulated structure is used as a starting foam and infused or impregnated with a ceramic slurry and then fired. Crushing strength is between 10 and 30 Kgf/cm2 or less. Bending strength is 5 Kgf/cm2 or less. Since the strengths are so weak, the ceramic foams are sometimes broken prior to use or in use.
The object of the invention is to provide a ceramic foam and a method for manufacturing the same in which strengths of the ceramic foam are improved so that it is not easily broken prior to use or in use.
The present invention is a ceramic foam having a three-dimensionally reticulated ceramic structure composed of many interconnected ceramic strands characterized in that a bulk density of the ceramic foam is between 0.4 and 2.0 and each of the strands has plural ceramic layers.
The present invention is also a method for manufacturing a ceramic foam comprising the steps of mixing a starting ceramic material with water and a binder thereby to form a slurry or slip, impregnating a starting foam having a three-dimensionally reticulated structure with the slurry or slip, drying them, and firing them thereby to obtain a ceramic body having a three-dimensionally reticulated ceramic structure composed of many interconnected ceramic strands characterized in that the impregnating and drying steps are repeated plural times thereby to form plural layers so as to adjust a thickness of the strands.
Even if a bulk density of the ceramic foam is slightly adjusted, strengths of the ceramic foam can be remarkably increased. A void ratio thereof is not so changed. Thus a molten metal can pass effectively through the ceramic foam.
Embodiments of the present invention will now be described, by way of example, with reference to the accompanying drawing in which Figures 1A, 1B, 1C, 1D and 1E are cross-sectional views showing a series of steps of a method for manufacturing a ceramic foam and particularly a strand thereof according to this invention.
Embodiment 1
First, a ceramic slip is prepared. A starting ceramic material including AT203 98% by weight is composed of small particles, sizes of which are between 0.1 and 44 micrometers, and a mean particle diameter of which is between 5 and 0.5 micrometers. The starting ceramic material is mixed with water and a rapid drying binder such as PVA by means of a ball mill so as to obtain a ceramic slurry or slip having a viscosity of 2-15 poise.
Also, a starting foam is prepared. A soft urethane foam is suitable thereas which has a three-dimensionally reticulated urethane structure composed of many interconnected strands. Figure 1A shows a cross-section of one strand 1 thereof.
As Figure 1B shows, a first ceramic layer 2 is formed on the urethane strand 1 by impregnating or infusing the strand 1 of the urethane foam with the slip. Surplus slip is removed. It is dried to be hardened at a temperature of 50-100 C.
Next, as shown in Figure 1C, a second ceramic layer 3 is formed on the first layer 2 by impregnating the first layer 2 with the slip. At this time, also, surplus slip is removed. It is again dried to be hardened as in the first layer 2.
In addition, as shown in Figure 1D, a third layer 4 is formed on the second layer 3 by infusing it with the slip. Surplus slip is removed. It is dried to be hardened in the same way.
Finally, in Figure 1E, the strands 5 consisting of the starting foam 1 and the ceramic layers 2,3,4 thereon are fired at a high temperature of 15000C or more. As a result, the ceramic layers 2, 3, 4 become a porcelain ceramic multi-layer as a ceramic strand 5'. Many of such a ceramic strand 5' are interconnected to constitute a three-dimensionally reticulated ceramic structure as in the starting foam. At the same time, the urethane strands 1 disappear on firing thereby to leave a long opening 6 in a central portion of each strand 5'.
A bulk density of the ceramic foam may be set so as to have a value of 0.4-2.0 by adjusting a thickness of the ceramic multi-layer of the strand 5.
In Table 1, a bulk density of the ceramic foam is between 0.4 and 2.0. Crushing strength is between 50 and 100 Kgf/cm2 and therefore remarkably increased in comparison with the prior art crushing strength of 10-30 Kgf/cm2 or less. Bending strength is between 10 and 35 Kgf/cm2, which is remarkably increased in comparison with the prior art of 5 Kgf/cm2 or less. Void ratio thereof is 85-90%, which is merely very slightly changed in comparison with the void ratios of the prior art. An apparent porosity of the ceramic strands 5' is 5% or less.
Embodiment 2
Although in the embodiment 1 the soft urethane foam 1 is impregnated with a common slip for the purpose of forming the first, second and third layers 2, 3, 4, a plurality of different slips are used for each layer according to the embodiment 2.
In the embodiment 2, a starting ceramic material is of AI203 98% by weight. The slip of the embodiment 1 may be used for a first layer 2, but other different slips of different sizes and blend ratios are used for a second layer 3 and a third layer 4.
For instance, for the first layer 2, a starting ceramic material is composed of small particles having particle sizes of 10-0.1 micrometers and an average particle diameter of 5-0-5 micrometers. A porosity of the first layer 2 of the ceramic strands 5' is to become 0%.
For the second layer 3, a starting ceramic material is composed of two groups of small particles: one having 70-90% by weight of particle sizes between 10 and 0.1 micrometers; and the other having 10-30% by weight of particle sizes between 44 and 10 micrometers. They are blended with water and a binder thereby to become a slip. A porosity of the second layer 3 of the ceramic strands 5' is to become 5-15%.
For the third layer 4, two groups of small particles are used, one of which has 50-70% by weight of particle sizes between 10 and 0.1 micrometers, and the other of which has 30-50% by weight of particle sizes between 44 and 10 micrometers. A porosity of the third layer 4 of the strands 5' is to become 1525%.
The impregnating, drying and firing steps in the embodiment 2 are substantially the same as in the embodiment 1.
A bulk density of the ceramic foam is between 0.4 and 2.0. Crushing strength and bending strength are substantially the same as those of the embodiment 1.
It is observed in the embodiment 2 that many fine pores having pore diameters of 50-1 micrometers are located in the ceramic strands 5'. Therefore, filtering efficiency is excellent.
Incidentally, the above-stated ceramic foam can have a catalytic function by holding active AI2O3("- AI2Os) or PT catalyst on the third layer 4. Holding power of the active Al2O3 or the like can be improved so as to increase lifetime due to the microporosity in the surface layer thereof.
Embodiment 3
In the embodiment 3, the chemical composition of a ceramic foam is Al2O3-ZrO2 unlike in the embodiments 1 and 2. In this embodiment, each ceramic strand 5' has an increased thickness in the same way as in the embodiments 1 and 2.
In the embodiment 3, a bulk density of the ceramic foam is 0.4-2.0 like in the embodiments 1 and 2.
The crushing strength and bending strength thereof have the same value as those of the embodiment 1.
Also, the void ratio and the pore diameter have the same as those of the embodiment 1. A thermal shock resistance of the embodiment 3 is better than that of the embodiment 1.
This invention is not limited to the embodiments as above-mentioned. For instance, as far as a bulk density of the ceramic foam is between 0;4 and 2.0, any number of layers can be formed. For example, only a first and second layers can be formed. If desired, a fourth layer and any other layer may be added.
Also, a starting ceramic material can be selected from SIC, Si3N4, Al203-SiO2, cordierite, and ZrO2.
If a bulk density of the ceramic foam is more than 2.0, void ratio is decreased too much so that a molten metal cannot easily pass through the continuous pores of the ceramic foam. Thus, filtering function is decreased.
TABLE 1
Items Embodiment 1 Embodiment 3
Chemical Composition 98% Al2O3 AI2O#-ZrO2 Bulk Density 0.4 - 2.0 0.4 - 2.0
Crushing Strength (Kgf/cm2) 50-100 50- 100
Bending Strength (Kgf/cm2) 10 - 35 10 - 35
Void Ratio 85 - 90 85- 90
Pore Diameter (mm) 1 - 2.5 1 - 2.5
Heating Resisting
Temperature ( C) 1700 or more 1700 or more
Apparent Porosity of Strands 5% or less 5% or less
Claims (21)
1. A ceramic foam having a three-dimensionally reticulated ceramic structure composed of many interconnected ceramic strands characterized in that a bulk density of the ceramic foam is between 0.4 and 2.0 and each of the strands has plural ceramic layers.
2. The ceramic foam of Claim 1, wherein an apparent porosity of the strands is 5% or less.
3. The ceramic foam of Claim 1, wherein the chemical composition of the strands in AI2Os.
4. The ceramic foam of Claim 1, wherein the chemical composition of the strands is AI2O#-ZrO2.
5. The ceramic foam of Claim 1, wherein the chemical composition of the strands is selected from
SiC, Si3N4, Al203-SiO2, cordierite, and ZrO2.
6. The ceramic foam of Claim 1, wherein void ratio of the ceramic foam is between 85% and 90%.
7. The ceramic foam of Claim 1, wherein the ceramic foam has pores having pore diameters between 1 mm and 2.5 mm.
8. The ceramic foam of Claim 1, wherein the strands have a large number of fine pores having sizes between 1 micrometer and 50 micrometers.
9. The ceramic foam of Claim 1, wherein the strands are composed of plural layers made of a common composition.
10. The ceramic foam of Claim 1, wherein the strands are composed of plural layers made of different compositions.
11. The ceramic foam of Claim 10, wherein the different compositions have different sizes and blend ratios thereof.
12. The ceramic foam of Claim 10, wherein the plural layers have different porosities, respectively.
13. The ceramic foam of Claim 2, wherein the plural layers include a first layer having a porosity of 0%, a second layer having a porosity of 5-15%, and a third layer having a porosity of 15-25%.
14. A method for manufacturing a ceramic foam comprising the steps of mixing a starting ceramic material with water and a binder thereby to form a slurry or slip, impregnating a starting foam having a three-dimensionally reticulated structure with the slurry or slip, drying them, and firing them thereby to obtain a ceramic body having a three-dimensionally reticulated ceramic structure composed of many interconnected ceramic strands characterized in that the impregnating and drying steps are repeated plural times thereby to form plural layers so as to adjust a thickness of the strands.
15. The method of Claim 14, wherein a common starting ceramic material is used for the plural layers.
16. The method of Claim 14, wherein the starting ceramic material is made of AI2O3 98% by weight and composed of small particles, sizes of which are between 0.1 and 44 micrometers, and a mean particle diameter of which is between 5 and 0.5 micrometers.
17. The method of Claim 14, wherein plural different starting ceramic materials are used for the plural layers.
18. The method of Claim 14, wherein the plural layers have a first, second and third layers, and wherein for the first layer the starting ceramic material is composed of small particles having particle sizes of 10-0.1 micrometers and an average particle diameter of 5-0.5 micrometers, and wherein for the second layer the starting ceramic material is composed of two groups of small particles: one having 7090% by weight of particle sizes between 10 and 0.1 micrometers; and the other having 10-30% by weight of particle sizes between 44 and 10 micrometers, and wherein for the third layer two groups of small particles are used, one of which has 50-70% by weight of particle sizes between 10 and 0.1 micrometers, and the other of which 30-50% by weight of particle sizes between 44 and 10 micrometers.
19. The method of Claim 14, wherein the slurry or slip has a viscosity of 2-15 poise.
20. A ceramic foam substantially as hereinbefore described with reference to, and as shown in, the accompanying drawing.
21. A method of making ceramic foam substantially as hereinbefore described with reference to the accompanying drawing.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP26089884A JPS61141682A (en) | 1984-12-12 | 1984-12-12 | Ceramic foam and manufacture |
Publications (3)
Publication Number | Publication Date |
---|---|
GB8527212D0 GB8527212D0 (en) | 1985-12-11 |
GB2168337A true GB2168337A (en) | 1986-06-18 |
GB2168337B GB2168337B (en) | 1988-05-25 |
Family
ID=17354287
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB08527212A Expired GB2168337B (en) | 1984-12-12 | 1985-11-05 | Ceramic foam |
Country Status (3)
Country | Link |
---|---|
JP (1) | JPS61141682A (en) |
DE (1) | DE3540449A1 (en) |
GB (1) | GB2168337B (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0419407A2 (en) * | 1989-09-18 | 1991-03-27 | Selee Corporation | Partially stabilized zirconia sintered body |
WO1991005973A1 (en) * | 1989-10-19 | 1991-05-02 | Morgan Materials Technology Limited | Gas heater |
GB2260538A (en) * | 1991-10-15 | 1993-04-21 | Peter Gant | Porous ceramics |
US6547967B1 (en) | 1997-12-01 | 2003-04-15 | Franhofer-Gesellschaft Zur Forderung Der Angewandten Forschung E.V. | Ceramic network, method for the production and utilization thereof |
WO2003053551A2 (en) * | 2001-12-08 | 2003-07-03 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | System and method for aftertreatment of exhaust gas produced by combustion engines |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2759147B2 (en) * | 1987-02-25 | 1998-05-28 | 住友化学工業株式会社 | Method for producing porous ceramic body |
DE3720963A1 (en) * | 1987-06-25 | 1989-01-05 | Metallgesellschaft Ag | Process and apparatus for separating off the ash from the gas arising in the combustion of coal |
US4866011A (en) * | 1988-05-02 | 1989-09-12 | Swiss Aluminium, Ltd. | Process for forming a ceramic foam |
DE19621638C2 (en) * | 1996-05-30 | 2002-06-27 | Fraunhofer Ges Forschung | Open cell foam ceramic with high strength and process for its production |
DE19805889C2 (en) * | 1998-02-13 | 2001-07-12 | Fraunhofer Ges Forschung | Sintered body based on corundum with a closed cell structure, its production and use |
DE10013378A1 (en) * | 2000-03-17 | 2001-10-04 | Dornier Gmbh | Porous ceramic comprises a three dimensional interconnected ceramic network and a three dimensional interconnected pore network, and has a bimodal size distribution |
DE10215734B4 (en) * | 2002-04-03 | 2013-08-01 | Hark Gmbh & Co Kg Kamin- Und Kachelofenbau | Process for treating exhaust gases from solid fuel fireplaces |
DE102008061644B4 (en) | 2008-12-12 | 2014-01-02 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Cellular material for high temperature applications and process for its preparation |
DE102008054596B4 (en) * | 2008-12-12 | 2011-04-14 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Open-cell ceramic and / or metal foam bodies with a rough, enveloping surface and process for their preparation |
DE102014110925A1 (en) | 2014-07-31 | 2016-02-04 | Otto-Von-Guericke-Universität Magdeburg | Process for the preparation of functionalized cellular materials |
DE102018116642A1 (en) | 2018-07-10 | 2020-01-16 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Open cell ceramic network and process for its manufacture |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2034298A (en) * | 1978-10-21 | 1980-06-04 | Bridgestone Tire Co Ltd | Ceramic porous bodies |
GB2062609A (en) * | 1979-10-30 | 1981-05-28 | Bridgestone Tire Co Ltd | Ceramic porous bodies |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3950175A (en) * | 1973-11-05 | 1976-04-13 | Corning Glass Works | Pore size control in cordierite ceramic |
JPS574710A (en) * | 1980-06-13 | 1982-01-11 | Mitsubishi Mining & Cement Co | Manufacture of ceramic porous body |
GB2082960B (en) * | 1980-07-15 | 1984-04-26 | Kobe Steel Ltd | Porous mouldings |
JPS5832090A (en) * | 1981-08-12 | 1983-02-24 | 株式会社ブリヂストン | Gas permeable heat insulator |
JPS57209892A (en) * | 1981-06-19 | 1982-12-23 | Bridgestone Tire Co Ltd | Gas permeable heat insulating material |
JPS59111967A (en) * | 1982-12-17 | 1984-06-28 | 株式会社ブリヂストン | Ceramic porous body |
JPS593059A (en) * | 1982-06-24 | 1984-01-09 | キヤタラ−工業株式会社 | Manufacture of cordierite ceramic foam |
JPS6011281A (en) * | 1983-06-24 | 1985-01-21 | キヤタラ−工業株式会社 | Ceramic three dimentional network structure and manufacture |
JPS6144778A (en) * | 1984-08-03 | 1986-03-04 | 株式会社デンソー | Manufacture of porous ceramic body |
JPS6158873A (en) * | 1984-08-30 | 1986-03-26 | 株式会社ブリヂストン | Manufacture of ceramic porous body |
-
1984
- 1984-12-12 JP JP26089884A patent/JPS61141682A/en active Granted
-
1985
- 1985-11-05 GB GB08527212A patent/GB2168337B/en not_active Expired
- 1985-11-14 DE DE19853540449 patent/DE3540449A1/en active Granted
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2034298A (en) * | 1978-10-21 | 1980-06-04 | Bridgestone Tire Co Ltd | Ceramic porous bodies |
GB2062609A (en) * | 1979-10-30 | 1981-05-28 | Bridgestone Tire Co Ltd | Ceramic porous bodies |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0419407A2 (en) * | 1989-09-18 | 1991-03-27 | Selee Corporation | Partially stabilized zirconia sintered body |
EP0419407A3 (en) * | 1989-09-18 | 1991-12-04 | Alusuisse-Lonza Services Ag | Partially stabilized zirconia sintered body |
WO1991005973A1 (en) * | 1989-10-19 | 1991-05-02 | Morgan Materials Technology Limited | Gas heater |
GB2260538A (en) * | 1991-10-15 | 1993-04-21 | Peter Gant | Porous ceramics |
GB2260538B (en) * | 1991-10-15 | 1995-08-16 | Peter Gant | Ceramic block for liquid retention |
US6547967B1 (en) | 1997-12-01 | 2003-04-15 | Franhofer-Gesellschaft Zur Forderung Der Angewandten Forschung E.V. | Ceramic network, method for the production and utilization thereof |
WO2003053551A2 (en) * | 2001-12-08 | 2003-07-03 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | System and method for aftertreatment of exhaust gas produced by combustion engines |
WO2003053551A3 (en) * | 2001-12-08 | 2003-09-18 | Fraunhofer Ges Forschung | System and method for aftertreatment of exhaust gas produced by combustion engines |
Also Published As
Publication number | Publication date |
---|---|
JPS61141682A (en) | 1986-06-28 |
DE3540449C2 (en) | 1989-06-29 |
GB2168337B (en) | 1988-05-25 |
DE3540449A1 (en) | 1986-06-12 |
GB8527212D0 (en) | 1985-12-11 |
JPH058148B2 (en) | 1993-02-01 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 19941105 |