[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

WO1995027556A1 - Process for producing membranes from nanoparticulate powders - Google Patents

Process for producing membranes from nanoparticulate powders Download PDF

Info

Publication number
WO1995027556A1
WO1995027556A1 PCT/US1995/004352 US9504352W WO9527556A1 WO 1995027556 A1 WO1995027556 A1 WO 1995027556A1 US 9504352 W US9504352 W US 9504352W WO 9527556 A1 WO9527556 A1 WO 9527556A1
Authority
WO
WIPO (PCT)
Prior art keywords
accordance
powder
nanometer
size
size particles
Prior art date
Application number
PCT/US1995/004352
Other languages
French (fr)
Inventor
Yong S. Zhen
Kenneth E. Hrdina
Original Assignee
Institute Of Gas Technology
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Institute Of Gas Technology filed Critical Institute Of Gas Technology
Priority to AU23811/95A priority Critical patent/AU2381195A/en
Publication of WO1995027556A1 publication Critical patent/WO1995027556A1/en

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D67/00Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
    • B01D67/0039Inorganic membrane manufacture
    • B01D67/0041Inorganic membrane manufacture by agglomeration of particles in the dry state
    • B01D67/00413Inorganic membrane manufacture by agglomeration of particles in the dry state by agglomeration of nanoparticles
    • 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
    • B01D39/2027Metallic material
    • B01D39/2031Metallic material the material being particulate
    • B01D39/2034Metallic material the material being particulate sintered or bonded by inorganic agents
    • 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D67/00Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
    • B01D67/0039Inorganic membrane manufacture
    • B01D67/0041Inorganic membrane manufacture by agglomeration of particles in the dry state
    • B01D67/00411Inorganic membrane manufacture by agglomeration of particles in the dry state by sintering
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D69/00Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor
    • B01D69/12Composite membranes; Ultra-thin membranes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D71/00Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
    • B01D71/02Inorganic material
    • B01D71/05Cermet materials
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F3/00Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
    • B22F3/10Sintering only
    • B22F3/11Making porous workpieces or articles
    • B22F3/1103Making porous workpieces or articles with particular physical characteristics
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F7/00Manufacture of composite layers, workpieces, or articles, comprising metallic powder, by sintering the powder, with or without compacting wherein at least one part is obtained by sintering or compression
    • B22F7/002Manufacture of composite layers, workpieces, or articles, comprising metallic powder, by sintering the powder, with or without compacting wherein at least one part is obtained by sintering or compression of porous nature
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2323/00Details relating to membrane preparation
    • B01D2323/08Specific temperatures applied
    • B01D2323/081Heating
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2323/00Details relating to membrane preparation
    • B01D2323/10Specific pressure applied
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F2998/00Supplementary information concerning processes or compositions relating to powder metallurgy
    • B22F2998/10Processes characterised by the sequence of their steps

Definitions

  • This invention relates to a process for producing structures, in particular, membranes, having Angstrom-size pores.
  • Membranes, in particular, prepared in accordance with the process of this invention are suitable for use in applications such as high temperature gas separation and as substrate materials for the deposition of ultra-thin ceramic or metal films.
  • Membrane technology is rapidly becoming an important research area in chemical engineering, especially in the separation of gases.
  • transport of fluids, solutes or molecules through membranes can occur by one of several different mechanisms.
  • the transport of any species through membranes which is similar to any separation process in chemical engineering, is driven by the difference in free energy or chemical potential of that species across the membrane.
  • the membranes encounter various combinations of harsh chemical environments and high temperatures. Thus, it is critical to evaluate the effects of changes in the thermal chemical properties and dimension stability of membrane materials on separation performance under different operating conditions.
  • Membrane processes have attracted much attention from an energy conservation stand-point in industrial gas separation processes.
  • the separation mechanisms of gases by porous solid membranes are conventionally classified into four types: 1) Knudsen diffusion, 2) surface diffusion, 3) capillary condensation with liquid flow, and 4) molecular sieving.
  • a narrow pore size distribution in a membrane system is needed in order to obtain a high degree of separation of mixtures, the required modal size depending on the type of mixture to be separated.
  • Conventional preparation of ceramic materials starts with powders produced either from synthetic reactions without strict chemical process control or by grinding up naturally occurring minerals. To prepare the final ceramics, powders are consolidated into porous compacts, then sintered into strong, dense ceramics. During these transformations, the grain size increases, pore shapes change, and the interior pores become smaller or disappear completely.
  • Ceramic membranes having ultra-fine pores are typically formed by so-called "wet processes,” that is, processes requiring the use of a solvent. Such processes include slip casting, gel casting, extrusion, and the sol- gel process.
  • the slip casting and gel casting processes utilize large amounts of solvents as well as dispersing agents to form a slurry which is then cast in a mold to form the desired membrane.
  • Extrusion typically involves the addition of a solvent along with die lubricants and an organic polymeric binder to a ceramic powder to form a mixture which is then extruded to form, typically, tubular membranes.
  • a solution of organo- metallic material is formed and then gelled. The solvent in the gel is then removed and the remaining structure heat treated.
  • Each of the slip casting, gel casting, extrusion and sol-gel processes utilize solvents and most of these processes utilize organic additives which must later be removed. This greatly limits the minimum size of the pores, typically submicron size, which can be formed in the resulting structure due to the requirement that the removal of solvents or organics requires that the pore size in the structure be larger than the molecules being removed.
  • Zeolites are a group of minerals, both naturally occurring and synthetically prepared, whose crystal structures contain pores on the order of about 3 to 20 Angstroms in size.
  • the preparation of monolithic discs or sheets of material using zeolite with only 3 to 20 Angstrom-size connected pores is not possible because the resulting micron size powder would contain crystals of zeolite which form shapes containing micron size pores with Angstrom-size pores within the crystals.
  • a process for producing a membrane having a plurality of Angstrom-size pores comprising the steps of forming a loose powder layer of at least one of a metal powder and a ceramic powder comprising a plurality of substantially all nanometer-size particles and compacting said loose powder layer of said at least one of said metal powder and said ceramic powder to form a consolidated powder porous membrane.
  • substantially all nanometer-size particles we mean a powder having greater than about 95% nanometer-size particles.
  • a critical feature of this process is the requirement that nanometer-size ceramic powders be utilized.
  • compacting of the nanometer-size particles is carried out by cold-isostatic pressing.
  • the nanoparticulate powder be relatively uniform in size.
  • the mean pore size of the membranes produced in accordance with the process of this invention can be controlled based upon the mean particle size of the powder being pressed. That is, the smaller the mean particle size of the powder, the smaller will be the mean pore size of the resulting membrane.
  • Membranes produced in accordance with this process have a higher porosity than those produced by other known processes for producing membranes, in particular, ceramic membranes.
  • membranes having a plurality of Angstrom-size pores are produced by compacting at least one of a metal powder and a ceramic powder comprising substantially all nanometer-size particles to form a consolidated porous layer of powder, that is, a consolidated powder porous membrane, the compacting being carried out by cold-isostatic pressing.
  • compaction pressures between about 15,000 psi and about 300,000 psi are preferred.
  • nanometer size particles having a narrow particle size distribution are desirable.
  • the metal and/or ceramic powder comprise at least about 98% nanometer-size particles and that at least 95% of the nanometer-size particles be less than about 30 nanometers.
  • the particle size of the nanometer-size particles is in the range of about 2 nanometers to about 30 nanometers.
  • the consolidated powder porous membranes produced in accordance with this process are strong, the particles being bonded as a result of cold welding and electrostatic forces.
  • the strength of the membrane can be increased by fast-firing the consolidated porous layer of powder.
  • a low sintering temperature minimizes the amount of densification taking place and, thus, maintains the large porosity present in the membrane.
  • a short hold time minimizes the amount of particle growth and, thus, reduces the amount of pore growth in the resulting membrane.
  • sintering temperatures required by the process of this invention are typically a few hundred degrees lower than the temperatures required to densify the ceramic.
  • alumina can be completely densified at 1550°C, but membranes produced in accordance with this process by compacting a ceramic powder comprising nanometer-size particles of alumina may be fired at 1000"C to strengthen it.
  • the consolidated porous layer of ceramic material resulting from compaction of the ceramic powder is fired at a temperature between about 800"C and about 2000 ⁇ C.
  • the hold time for the membrane within the firing process is less than 30 minutes and, preferably less than 5 minutes.
  • a heating rate of about 0.5 ⁇ C/minute to about 2000 ⁇ C/minute is preferred.
  • YSZ Y 2 0 3 -doped Zr0 2
  • the membranes can be heat treated by fast-firing to preserve the uniformity of the pore size distribution.
  • Membranes produced in accordance with the process of this invention have a porosity of about 30% to 55%, that is, about 30% to about 55% porous.
  • the mean pore radius of the membranes produced in accordance with the process of this invention is between about 1/5 to 1/20 of the mean particle diameter of the powder used. In other words, if a powder with a mean particle diameter of 10 nanometers is used, a membrane with a mean pore radius of about 5 Angstroms will be obtained. If membrane support or multilayers of membranes are desired, powders of different particulate size can be pressed together to form membrane layers of different mean pore sizes.
  • the loose powder layer of nanometer- size particles of metal powder and/or ceramic powder is formed on a coarse particle layer of metal and/or ceramic powder particles where the coarse particle layer comprises a plurality of particles, substantially all larger than nanometer-size.
  • the loose powder layer and the coarse particle layer are simultaneously compacted together, forming a multilayer consolidated powder porous membrane.
  • the coarse particle layer is compacted and the loose powder layer is formed on the compacted coarse particle layer and subsequently compacted onto the compacted coarse particle layer to form a multilayer consolidated powder porous membrane.
  • This example demonstrates a method for making a ceramic membrane having a two-layer structure.
  • YSZ submicron size 8 mol percent Y 2 0 3 -doped Zr0 2
  • the membrane prepared in this example was found to be effective in the separation of H 2 /C0 2 mixture.
  • the membrane was found to be at least four times more permeable to H 2 than to C0 2 .
  • the gas transfusing rate across the membrane was significantly enhanced in the two-layer membrane structure compared to that of Example I.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Mechanical Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Geology (AREA)
  • Nanotechnology (AREA)
  • Ceramic Engineering (AREA)
  • Composite Materials (AREA)
  • Materials Engineering (AREA)
  • Separation Using Semi-Permeable Membranes (AREA)

Abstract

A process for producing a membrane having a plurality of Angstrom-size pores in which a powder comprising nanometer-size particles is compacted to form a consolidated powder porous membrane. In accordance with a preferred embodiment, the powder is compacted by cold-isostatic pressing.

Description

PROCESS FOR PRODUCING MEMBRANES FROM NANOPARTICULATE POWDERS
BACKGROUND OF THE INVENTION Field of the Invention
This invention relates to a process for producing structures, in particular, membranes, having Angstrom-size pores. Membranes, in particular, prepared in accordance with the process of this invention are suitable for use in applications such as high temperature gas separation and as substrate materials for the deposition of ultra-thin ceramic or metal films.
Description of Prior Art
Membrane technology is rapidly becoming an important research area in chemical engineering, especially in the separation of gases. Depending on the structure and nature of the materials, transport of fluids, solutes or molecules through membranes can occur by one of several different mechanisms. The transport of any species through membranes, which is similar to any separation process in chemical engineering, is driven by the difference in free energy or chemical potential of that species across the membrane. In actual use, the membranes encounter various combinations of harsh chemical environments and high temperatures. Thus, it is critical to evaluate the effects of changes in the thermal chemical properties and dimension stability of membrane materials on separation performance under different operating conditions.
The primary deficiency of the current generation of ceramic membranes is their poor damage tolerance and long-term reliability. On the other hand, the main advantages of ceramic materials over conventional metals in the primary structural applications are their superior strength and, at high temperatures, good thermal stress resistance, and excellent oxidation, corrosion, and erosion resistance. Unfortunately, the brittleness of ceramics has restricted their use in these applications where materials toughness is an important criterion. In addition, ceramic materials are susceptible to thermal stresses and thermal shock failure, failures often occurring at temperatures that are lower than the service temperatures during heating and cooling.
Membrane processes have attracted much attention from an energy conservation stand-point in industrial gas separation processes. The separation mechanisms of gases by porous solid membranes are conventionally classified into four types: 1) Knudsen diffusion, 2) surface diffusion, 3) capillary condensation with liquid flow, and 4) molecular sieving. In general, a narrow pore size distribution in a membrane system is needed in order to obtain a high degree of separation of mixtures, the required modal size depending on the type of mixture to be separated. Conventional preparation of ceramic materials starts with powders produced either from synthetic reactions without strict chemical process control or by grinding up naturally occurring minerals. To prepare the final ceramics, powders are consolidated into porous compacts, then sintered into strong, dense ceramics. During these transformations, the grain size increases, pore shapes change, and the interior pores become smaller or disappear completely.
Ceramic membranes having ultra-fine pores are typically formed by so-called "wet processes," that is, processes requiring the use of a solvent. Such processes include slip casting, gel casting, extrusion, and the sol- gel process. The slip casting and gel casting processes utilize large amounts of solvents as well as dispersing agents to form a slurry which is then cast in a mold to form the desired membrane. Extrusion typically involves the addition of a solvent along with die lubricants and an organic polymeric binder to a ceramic powder to form a mixture which is then extruded to form, typically, tubular membranes. In the sol-gel process, a solution of organo- metallic material is formed and then gelled. The solvent in the gel is then removed and the remaining structure heat treated.
Each of the slip casting, gel casting, extrusion and sol-gel processes utilize solvents and most of these processes utilize organic additives which must later be removed. This greatly limits the minimum size of the pores, typically submicron size, which can be formed in the resulting structure due to the requirement that the removal of solvents or organics requires that the pore size in the structure be larger than the molecules being removed.
In addition, the removal of solvents produces capillary stresses in the structure which increase as the pore size of the structure decreases. To avoid cracks in the submicron pore size structures, elaborate and expensive drying schemes are required. When nanosize or Angstrom-size pores are desired, the problem becomes essentially insurmountable due to the tremendous capillary stresses encountered. See Hsieh, H.P. et al., "Microporous Ceramic Membranes", Polvmer Journal. Volume 23, No. 5, pages 407-415 (1991) which teaches conventional ceramic forming techniques such as extrusion, compression and injection molding which can be used to produce ceramic membranes with symmetric structures and large pores from particles of well controlled size distributions. See also Chan K. et al., "Ceramic Membranes-Growth Prospects and Opportunities", Ceramic Bulletin. Volume 70, No. 4, (1991) which teaches the use of the sol-gel process for producing membranes having submicron pore sizes; Zievers, J. F. et al., "Porous Ceramics For Gas Filtration", Ceramic Bulletin. Volume 70, No. 1, pages 108- 111, (1991) which teaches the use of layered porous ceramic filter elements for gas filtration; and Breck, D. W. et al., "Molecular Sieves", Scientific American (1959) which teaches the use of molecular sieves for separating very similar molecules.
Zeolites are a group of minerals, both naturally occurring and synthetically prepared, whose crystal structures contain pores on the order of about 3 to 20 Angstroms in size. However, the preparation of monolithic discs or sheets of material using zeolite with only 3 to 20 Angstrom-size connected pores is not possible because the resulting micron size powder would contain crystals of zeolite which form shapes containing micron size pores with Angstrom-size pores within the crystals.
SUMMARY OF THE INVENTION
Accordingly, it is an objection of this invention to provide a process for producing a monolithic structure having Angstrom-size and nanosize pores.
It is another object of this invention to produce ceramic and/or metal membranes having nanosize and Angstrom- size pores.
It is yet another object of this invention to provide a process for producing ceramic and/or metal membranes which requires no solvents or dispersants which can require elaborate and expensive drying schemes to avoid cracks in the resulting submicron structure.
It is yet another object of this invention to provide a process for producing ceramic and/or metal membranes which avoids the use of organic additives or solvents which must be removed during the manufacturing process and, thus, limit the minimum pore size obtainable to the size of the molecules being removed from the final product.
These and other objects of this invention are achieved by a process for producing a membrane having a plurality of Angstrom-size pores comprising the steps of forming a loose powder layer of at least one of a metal powder and a ceramic powder comprising a plurality of substantially all nanometer-size particles and compacting said loose powder layer of said at least one of said metal powder and said ceramic powder to form a consolidated powder porous membrane. By "substantially all nanometer-size particles," we mean a powder having greater than about 95% nanometer-size particles. A critical feature of this process is the requirement that nanometer-size ceramic powders be utilized. In a preferred embodiment of the process of this invention, compacting of the nanometer-size particles is carried out by cold-isostatic pressing.
To form membranes having highly uniform nanometer- size pores, it is generally desired that the nanoparticulate powder be relatively uniform in size. In addition, the mean pore size of the membranes produced in accordance with the process of this invention can be controlled based upon the mean particle size of the powder being pressed. That is, the smaller the mean particle size of the powder, the smaller will be the mean pore size of the resulting membrane. Membranes produced in accordance with this process have a higher porosity than those produced by other known processes for producing membranes, in particular, ceramic membranes.
DESCRIPTION OF PREFERRED EMBODIMENTS
In accordance with a preferred embodiment of this invention, membranes having a plurality of Angstrom-size pores are produced by compacting at least one of a metal powder and a ceramic powder comprising substantially all nanometer-size particles to form a consolidated porous layer of powder, that is, a consolidated powder porous membrane, the compacting being carried out by cold-isostatic pressing. To eliminate large pores from within the resulting structure, that is, pores greater than about three (3) times the particle size employed, compaction pressures between about 15,000 psi and about 300,000 psi are preferred.
To produce a membrane having uniform pore sizes in accordance with the process of this invention, nanometer size particles having a narrow particle size distribution are desirable. In particular, it is preferred that the metal and/or ceramic powder comprise at least about 98% nanometer-size particles and that at least 95% of the nanometer-size particles be less than about 30 nanometers. In a particularly preferred embodiment, the particle size of the nanometer-size particles is in the range of about 2 nanometers to about 30 nanometers.
The consolidated powder porous membranes produced in accordance with this process are strong, the particles being bonded as a result of cold welding and electrostatic forces. In accordance with another preferred embodiment of this invention, the strength of the membrane can be increased by fast-firing the consolidated porous layer of powder. However, there are two important heating conditions which must be observed - a low sintering temperature and a short hold time. A low sintering temperature minimizes the amount of densification taking place and, thus, maintains the large porosity present in the membrane. A short hold time minimizes the amount of particle growth and, thus, reduces the amount of pore growth in the resulting membrane.
For ceramic membranes, sintering temperatures required by the process of this invention are typically a few hundred degrees lower than the temperatures required to densify the ceramic. For example, alumina can be completely densified at 1550°C, but membranes produced in accordance with this process by compacting a ceramic powder comprising nanometer-size particles of alumina may be fired at 1000"C to strengthen it. In a preferred embodiment of the process of this invention, the consolidated porous layer of ceramic material resulting from compaction of the ceramic powder is fired at a temperature between about 800"C and about 2000βC.
In accordance with a preferred embodiment of this invention, the hold time for the membrane within the firing process is less than 30 minutes and, preferably less than 5 minutes. Correspondingly, a heating rate of about 0.5βC/minute to about 2000βC/minute is preferred. Upon completion of the firing process, the resulting membrane is cooled, preferably as quickly as possible without causing damage to the membrane.
EXAMPLE I
Approximately 4 grams of nanoparticulate 8 mol percent Y203-doped Zr02 (YSZ) powder having a mean diameter of about 20 nanometers was die-pressed to form a disc of about 2.25" in diameter. The ceramic disc was then cold- isostatically pressed at 55,000 psi. Pore-size distribution analysis of the pressed YSZ disc indicated that it was about 50% porous with a uniform distribution of pores. The mean pore radius of the membrane was determined to be about 27 Angstroms. In a gas separation test, the membrane prepared in accordance with this example was found to be effective in the separation of an H2/C02 gas mixture. The membrane was found to be at least four times more permeable to H2 than to C02.
It will be apparent to those skilled in the art that different membrane shapes can be formed in accordance with the process of this invention including discs and tubes.
To improve the mechanical strength, the membranes can be heat treated by fast-firing to preserve the uniformity of the pore size distribution. Membranes produced in accordance with the process of this invention have a porosity of about 30% to 55%, that is, about 30% to about 55% porous. The mean pore radius of the membranes produced in accordance with the process of this invention is between about 1/5 to 1/20 of the mean particle diameter of the powder used. In other words, if a powder with a mean particle diameter of 10 nanometers is used, a membrane with a mean pore radius of about 5 Angstroms will be obtained. If membrane support or multilayers of membranes are desired, powders of different particulate size can be pressed together to form membrane layers of different mean pore sizes. In particular, in accordance with one embodiment of the process of this invention for producing multilayer membranes, the loose powder layer of nanometer- size particles of metal powder and/or ceramic powder is formed on a coarse particle layer of metal and/or ceramic powder particles where the coarse particle layer comprises a plurality of particles, substantially all larger than nanometer-size. In accordance with one embodiment of the process of this invention, the loose powder layer and the coarse particle layer are simultaneously compacted together, forming a multilayer consolidated powder porous membrane, In accordance with another embodiment of the process of this invention, the coarse particle layer is compacted and the loose powder layer is formed on the compacted coarse particle layer and subsequently compacted onto the compacted coarse particle layer to form a multilayer consolidated powder porous membrane. EXAMPLE II
This example demonstrates a method for making a ceramic membrane having a two-layer structure.
Approximately 4 grams of submicron size 8 mol percent Y203-doped Zr02 (YSZ) powder having a mean diameter of about 0.3 microns were die-pressed to form a disc of 2.25" in diameter. Before removal of the YSZ disc from the stainless steel die, approximately 0.2 g of nanoparticluate A1203 powder having a mean diameter of about 10 nanometers were spread evenly on the top surface of the YSZ disc, and die-pressed once again to form a two-layer porous structure. The two-layer ceramic structure was them cold-isostatically pressed at 58,000 psi. Accordingly, the YSZ powder, in this case, was used as the supporting structure for the thin A1203 membrane.
In a gas separation test, the membrane prepared in this example was found to be effective in the separation of H2/C02 mixture. The membrane was found to be at least four times more permeable to H2 than to C02. The gas transfusing rate across the membrane was significantly enhanced in the two-layer membrane structure compared to that of Example I.
While in the foregoing specification this invention has been described in relation to certain preferred embodiments thereof, and many details have been set forth for purpose of illustration, it will be apparent to those skilled in the art that the invention is susceptible to additional embodiments and that certain of the details described herein can be varied considerably without departing from the basic principles of the invention.

Claims

WE CLAIM:
1. A process for producing a membrane having a plurality of Angstrom-size pores comprising the steps of: forming a loose powder layer of at least one of a metal powder and a ceramic powder comprising a plurality of substantially all nanometer-size particles; and compacting said loose powder layer of said at least one of said metal powder and said ceramic powder, forming a consolidated powder porous membrane.
2. A process in accordance with Claim 1, wherein said loose powder layer is compacted by cold-isostatic pressing.
3. A process in accordance with Claim 1, wherein said consolidated powder porous membrane is fired at a heating rate between about 0.5°C/minute and about 2000°C/minute.
4. A process in accordance with Claim 3, wherein said consolidated powder porous membrane is fired at a temperature between about 800°C and about 2000°C.
5. A process in accordance with Claim 1, wherein said at least one of said metal powder and said ceramic powder comprises at least about 98% said nanometer-size particles.
6. A process in accordance with Claim 5, wherein at least 95% of said nanometer-size particles are less than about 30 nanometers.
7. A process in accordance with Claim 1, wherein said compaction pressure is between about 15,000 psi and about 300,000 psi.
8. A process in accordance with Claim 6, wherein said compaction pressure is between about 30,000 psi and about 150,000 psi.
9. A process in accordance with Claim 5, wherein the particle size of said nanometer-size particles is in the range of about 2 nanometers to about 30 nanometers.
10. A process in accordance with Claim 1, wherein the pore sizes of said consolidated powder porous membrane are in the range of about 1 Angstrom to about three times the largest of said nanometer-size particles.
11. A process in accordance with Claim 10, wherein the particle size of said nanometer-size particles is in the range of about 2 nanometers to about 30 nanometers.
12. A process in accordance with Claim 1, wherein said loose powder layer of said at least one of said metal powder and said ceramic powder comprising a plurality of substantially all nanometer-size particles is formed on a coarse particle layer of said at least one of said metal powder and said ceramic powder, said coarse particle layer comprising a plurality of particles larger than nanometer- size.
13. A process in accordance with Claim 12, wherein said loose powder layer and said coarse particle layer are simultaneously compacted together, forming a multilayer said consolidated powder porous membrane.
14. A process in accordance with Claim 12, wherein said coarse particle layer is compacted prior to forming of said loose powder layer and said loose powder layer is compacted onto said coarse particle layer, forming a multilayer said consolidated powder porous membrane.
15. In a process for producing a porous structure from powders in which said powders are compacted to form said porous structure, the improvement comprising: said powders comprising a plurality of substantially all nanometer-size particles.
16. In a process in accordance with Claim 15, wherein at least 95% of said nanometer-size particles are less than about 30 nanometers.
17. In a process in accordance with Claim 16, wherein the particle size of said nanometer-size particles is in the range of about 2 nanometers to about 30 nanometers.
18. In a process in accordance with Claim 15, wherein the pore sizes of said structures are in the range of about 1 Angstrom to about three times the largest of said nanometer-size particles.
19. In a process in accordance with Claim 15, wherein said powders are compacted by cold-isostatic pressing.
20. In a process in accordance with Claim 15, wherein said porous structures are fired at a heating rate between about 0.5°C/minute and about 2000°C/minute.
21. In a process in accordance with Claim 20, wherein said powder is fired at a temperature between about 800°C and about 2000°C.
22. In a process in accordance with Claim 15, wherein said nanometer-size particles are compacted onto a substrate porous structure, forming a multilayer said porous structure.
PCT/US1995/004352 1994-04-07 1995-04-07 Process for producing membranes from nanoparticulate powders WO1995027556A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU23811/95A AU2381195A (en) 1994-04-07 1995-04-07 Process for producing membranes from nanoparticulate powders

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US22525694A 1994-04-07 1994-04-07
US08/225,256 1994-04-07

Publications (1)

Publication Number Publication Date
WO1995027556A1 true WO1995027556A1 (en) 1995-10-19

Family

ID=22844180

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1995/004352 WO1995027556A1 (en) 1994-04-07 1995-04-07 Process for producing membranes from nanoparticulate powders

Country Status (3)

Country Link
AU (1) AU2381195A (en)
CA (1) CA2187330A1 (en)
WO (1) WO1995027556A1 (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997047419A1 (en) * 1996-06-11 1997-12-18 British Nuclear Fuels Plc Manufacture of articles with controlled density distribution
WO1999003559A1 (en) * 1997-07-18 1999-01-28 N.V. Bekaert S.A. Sintered metal fiber for use in the preparation of beverages
WO1999011362A1 (en) * 1997-09-03 1999-03-11 Filterwerk Mann+Hummel Gmbh Filter element having a filter active structure coated with a nanoceramic layer
WO2000076634A1 (en) * 1999-06-11 2000-12-21 Gas Separation Technology, Inc. Porous gas permeable material for gas separation
EP1569790A2 (en) * 2002-12-12 2005-09-07 Mykrolis Corporation Porous sintered composite materials
RU2518809C2 (en) * 2012-03-29 2014-06-10 Государственное бюджетное образовательное учреждение высшего профессионального образования "Самарский государственный медицинский университет" Министерства здравоохранения Российской Федерации Method of producing high-porosity materials

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2150390A1 (en) * 1971-08-24 1973-04-06 Montedison Spa
US4329157A (en) * 1978-05-16 1982-05-11 Monsanto Company Inorganic anisotropic hollow fibers
WO1990000685A1 (en) * 1988-07-06 1990-01-25 Interelectric Ag Process for manufacturing a radial bearing
EP0426546A2 (en) * 1989-10-26 1991-05-08 Toto Ltd. Ceramic filter and process for making it
EP0467735A1 (en) * 1990-07-03 1992-01-22 Alcoa Separations Technology Inc. Pyrogen separations by ceramic ultrafiltration
EP0580134A1 (en) * 1992-07-21 1994-01-26 Toshiba Tungaloy Co. Ltd. Process for preparing a hard sintered alloy having fine pores
WO1995005256A1 (en) * 1993-08-17 1995-02-23 Ultram International, L.L.C. Process for the production of porous membranes

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2150390A1 (en) * 1971-08-24 1973-04-06 Montedison Spa
US4329157A (en) * 1978-05-16 1982-05-11 Monsanto Company Inorganic anisotropic hollow fibers
WO1990000685A1 (en) * 1988-07-06 1990-01-25 Interelectric Ag Process for manufacturing a radial bearing
EP0426546A2 (en) * 1989-10-26 1991-05-08 Toto Ltd. Ceramic filter and process for making it
EP0467735A1 (en) * 1990-07-03 1992-01-22 Alcoa Separations Technology Inc. Pyrogen separations by ceramic ultrafiltration
EP0580134A1 (en) * 1992-07-21 1994-01-26 Toshiba Tungaloy Co. Ltd. Process for preparing a hard sintered alloy having fine pores
WO1995005256A1 (en) * 1993-08-17 1995-02-23 Ultram International, L.L.C. Process for the production of porous membranes

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997047419A1 (en) * 1996-06-11 1997-12-18 British Nuclear Fuels Plc Manufacture of articles with controlled density distribution
WO1999003559A1 (en) * 1997-07-18 1999-01-28 N.V. Bekaert S.A. Sintered metal fiber for use in the preparation of beverages
WO1999011362A1 (en) * 1997-09-03 1999-03-11 Filterwerk Mann+Hummel Gmbh Filter element having a filter active structure coated with a nanoceramic layer
US6866697B2 (en) * 1999-06-11 2005-03-15 Gas Separation Technology, Inc. Porous gas permeable material for gas separation
US6425936B1 (en) 1999-06-11 2002-07-30 Gas Separatation Technology, Inc. Porous gas permeable material for gas separation
US6558455B2 (en) * 1999-06-11 2003-05-06 Gas Separation Technology Inc. Porous gas permeable material for gas separation
WO2000076634A1 (en) * 1999-06-11 2000-12-21 Gas Separation Technology, Inc. Porous gas permeable material for gas separation
US7314504B2 (en) 1999-06-11 2008-01-01 Gas Separation Technology, Inc. Porous gas permeable material for gas separation
EP1569790A2 (en) * 2002-12-12 2005-09-07 Mykrolis Corporation Porous sintered composite materials
EP1569790A4 (en) * 2002-12-12 2006-09-20 Entegris Inc Porous sintered composite materials
US7329311B2 (en) 2002-12-12 2008-02-12 Entegris, In. Porous sintered composite materials
US7534287B2 (en) 2002-12-12 2009-05-19 Entegris, Inc. Porous sintered composite materials
RU2518809C2 (en) * 2012-03-29 2014-06-10 Государственное бюджетное образовательное учреждение высшего профессионального образования "Самарский государственный медицинский университет" Министерства здравоохранения Российской Федерации Method of producing high-porosity materials

Also Published As

Publication number Publication date
CA2187330A1 (en) 1995-10-19
AU2381195A (en) 1995-10-30

Similar Documents

Publication Publication Date Title
EP1483421B1 (en) Reaction bonded alumina filter and membrane support
US6576182B1 (en) Process for producing shrinkage-matched ceramic composites
US8293143B2 (en) Method of preparing a thin ceramic composition with two materials, the composition thus obtained and the constituent electrochemical cell and membrane
US7223356B2 (en) Method for preparing a thin ceramic material with controlled surface porosity gradient, and resulting ceramic material
US6719947B1 (en) Composite porous media
US5733499A (en) Method for producing ceramic substrate
EP1341739B1 (en) Open-celled silicon carbide foam ceramic and method for production thereof
US5143614A (en) Membrane device for filtration, separation, or catalytic reaction
US7306642B2 (en) High CTE reaction-bonded ceramic membrane supports
CN109396446B (en) Hierarchical porous composite material filter body and preparation method thereof
Wang et al. Porous α-Al2O3 ceramics prepared by gelcasting
US6551369B1 (en) Ceramic flat membrane and method for producing the same
WO1995027556A1 (en) Process for producing membranes from nanoparticulate powders
JPH0859367A (en) Preparation of porous ceramic or porous ceramic laminated body by using hollow spherical polymeric precursor
US6978901B1 (en) Ceramic multilayer filters and method for producing the same
CN100337728C (en) Multilayer ceramic composite
Novich et al. Consolidation behavior of high‐performance ceramic suspensions
Takebe et al. Fabrication of zirconia-nickel functionally gradient materials by slip casting and pressureless-sintering
US5656168A (en) Method of fabricating inorganic filter structures
JP2958472B2 (en) High strength porous member and method of manufacturing the same
WO1998011974A1 (en) Porous nickel filter material
US20240157309A1 (en) Sintered porous body with multiple layers
JPS6183689A (en) Silicon carbide base honeycomb structure
JP2934865B2 (en) Silica glass filter
Antsiferov et al. Ceramic membranes from reaction-sintered silicon nitride on nitride and oxide substrates

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AM AT AU BB BG BR BY CA CH CN CZ DE DK EE ES FI GB GE HU JP KE KG KP KR KZ LK LR LT LU LV MD MG MN MW MX NO NZ PL PT RO RU SD SE SI SK TJ TT UA UZ VN

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): KE MW SD SZ UG AT BE CH DE DK ES FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
WWE Wipo information: entry into national phase

Ref document number: 2187330

Country of ref document: CA

REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

122 Ep: pct application non-entry in european phase