CA2074349C - Polytetrafluoroethylene porous film and preparation and use thereof - Google Patents
Polytetrafluoroethylene porous film and preparation and use thereof Download PDFInfo
- Publication number
- CA2074349C CA2074349C CA002074349A CA2074349A CA2074349C CA 2074349 C CA2074349 C CA 2074349C CA 002074349 A CA002074349 A CA 002074349A CA 2074349 A CA2074349 A CA 2074349A CA 2074349 C CA2074349 C CA 2074349C
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- Prior art keywords
- polytetrafluoroethylene
- delta
- film
- porous film
- semisintered
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- 239000004810 polytetrafluoroethylene Substances 0.000 title claims abstract description 105
- 229920001343 polytetrafluoroethylene Polymers 0.000 title claims abstract description 104
- -1 Polytetrafluoroethylene Polymers 0.000 title claims abstract description 37
- 238000002360 preparation method Methods 0.000 title description 2
- 239000000463 material Substances 0.000 claims abstract description 64
- 239000011148 porous material Substances 0.000 claims abstract description 35
- 238000002844 melting Methods 0.000 claims abstract description 23
- 230000008018 melting Effects 0.000 claims abstract description 23
- 238000010438 heat treatment Methods 0.000 claims abstract description 12
- 238000005245 sintering Methods 0.000 claims description 16
- 230000004927 fusion Effects 0.000 claims description 15
- 239000012779 reinforcing material Substances 0.000 claims description 10
- 238000009998 heat setting Methods 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 239000000853 adhesive Substances 0.000 claims description 3
- 230000001070 adhesive effect Effects 0.000 claims description 3
- 229940058401 polytetrafluoroethylene Drugs 0.000 description 79
- 239000002245 particle Substances 0.000 description 17
- 239000004745 nonwoven fabric Substances 0.000 description 9
- 239000000835 fiber Substances 0.000 description 7
- 230000002093 peripheral effect Effects 0.000 description 7
- 229920001410 Microfiber Polymers 0.000 description 6
- 230000007423 decrease Effects 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 230000007246 mechanism Effects 0.000 description 6
- 239000003658 microfiber Substances 0.000 description 6
- 238000010030 laminating Methods 0.000 description 5
- 238000004804 winding Methods 0.000 description 5
- 239000011230 binding agent Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 4
- 230000033001 locomotion Effects 0.000 description 3
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000010410 dusting Methods 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 238000003475 lamination Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 239000011164 primary particle Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 2
- 239000011882 ultra-fine particle Substances 0.000 description 2
- 101100446726 Caenorhabditis elegans flh-2 gene Proteins 0.000 description 1
- 244000228957 Ferula foetida Species 0.000 description 1
- 241000221931 Hypomyces rosellus Species 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 229920006361 Polyflon Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 206010038776 Retching Diseases 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 238000003490 calendering Methods 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000003889 chemical engineering Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000003795 desorption Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000011295 pitch Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 230000003405 preventing effect Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001360 synchronised effect Effects 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
-
- 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
- B01D39/16—Other self-supporting filtering material ; Other filtering material of organic material, e.g. synthetic fibres
- B01D39/1692—Other shaped material, e.g. perforated or porous sheets
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D67/00—Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
- B01D67/0002—Organic membrane manufacture
- B01D67/0023—Organic membrane manufacture by inducing porosity into non porous precursor membranes
- B01D67/0025—Organic membrane manufacture by inducing porosity into non porous precursor membranes by mechanical treatment, e.g. pore-stretching
- B01D67/0027—Organic membrane manufacture by inducing porosity into non porous precursor membranes by mechanical treatment, e.g. pore-stretching by stretching
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D69/00—Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor
- B01D69/10—Supported membranes; Membrane supports
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D69/00—Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor
- B01D69/10—Supported membranes; Membrane supports
- B01D69/107—Organic support material
- B01D69/1071—Woven, non-woven or net mesh
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
- B01D71/06—Organic material
- B01D71/30—Polyalkenyl halides
- B01D71/32—Polyalkenyl halides containing fluorine atoms
- B01D71/36—Polytetrafluoroethene
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C55/00—Shaping by stretching, e.g. drawing through a die; Apparatus therefor
- B29C55/005—Shaping by stretching, e.g. drawing through a die; Apparatus therefor characterised by the choice of materials
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2323/00—Details relating to membrane preparation
- B01D2323/08—Specific temperatures applied
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2323/00—Details relating to membrane preparation
- B01D2323/08—Specific temperatures applied
- B01D2323/081—Heating
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2325/00—Details relating to properties of membranes
- B01D2325/02—Details relating to pores or porosity of the membranes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2325/00—Details relating to properties of membranes
- B01D2325/02—Details relating to pores or porosity of the membranes
- B01D2325/0281—Fibril, or microfibril structures
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2027/00—Use of polyvinylhalogenides or derivatives thereof as moulding material
- B29K2027/12—Use of polyvinylhalogenides or derivatives thereof as moulding material containing fluorine
- B29K2027/18—PTFE, i.e. polytetrafluorethene, e.g. ePTFE, i.e. expanded polytetrafluorethene
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/04—Condition, form or state of moulded material or of the material to be shaped cellular or porous
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2327/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers
- C08J2327/02—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment
- C08J2327/12—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C08J2327/18—Homopolymers or copolymers of tetrafluoroethylene
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S264/00—Plastic and nonmetallic article shaping or treating: processes
- Y10S264/73—Processes of stretching
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24273—Structurally defined web or sheet [e.g., overall dimension, etc.] including aperture
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/249921—Web or sheet containing structurally defined element or component
- Y10T428/249953—Composite having voids in a component [e.g., porous, cellular, etc.]
- Y10T428/249978—Voids specified as micro
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/249921—Web or sheet containing structurally defined element or component
- Y10T428/249953—Composite having voids in a component [e.g., porous, cellular, etc.]
- Y10T428/249978—Voids specified as micro
- Y10T428/249979—Specified thickness of void-containing component [absolute or relative] or numerical cell dimension
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/3154—Of fluorinated addition polymer from unsaturated monomers
- Y10T428/31544—Addition polymer is perhalogenated
Abstract
The present invention is directed to a polytetrafluoroethylene porous film, which is prepared by stretching a semisintered polytetrafluoroethylene material and heating the stretched material at a temperature higher than the melting point of sintered polytetrafluoroethylene. It has an area ratio of fibrils to nodes of from 99:1 to 75:25, an average fibril diameter of from 0.05 to 0.2 Vim, a largest node area of not larger than 2µm2 and an average pore size of from 0.2 to 0.5 µm and achieves low pressure loss.
Description
Polytetrafluoroethvlene Porous Film and Preparation and Use Thereof The present invention relates to a polytetra-fluoroethylene (hereinafter referred to as "PTFE") porous film, a process for preparing the same and a filter compri-sing the same. More particularly, the present invention relates to a novel PTFE porous film useful as an air filter which is suitable for trapping suspended fine particles in air or other gases in an clean room to be used in a semi-conductor indusv~ry and which causes a small pressure loss of the air or other gases. .
As a material for an air filter to be used in a clean room, a filter material prepared by forming a sheet from a mixture of glass fibers and a binder is often used. However, such a filter material has some drawbacks, for example, the presence of adhered minute fibers in the filter material, occurrence of self-dusting during processing or folding of the filter material, or an increase in pressure loss because an increased amount of binder is added to suppress the self-dusting (cf.
Japanese Patent Kokai Publication No. 16019/1988 and corresponding U.S. Patent No. 4,877,433). In addition, when such a filter material is contacted with a certain chemical such a,s hydrofluoric acid, it creates dust due to deterioratio:a of the glass and the binder.
As a material for an air filter to be used in a clean room, a filter material prepared by forming a sheet from a mixture of glass fibers and a binder is often used. However, such a filter material has some drawbacks, for example, the presence of adhered minute fibers in the filter material, occurrence of self-dusting during processing or folding of the filter material, or an increase in pressure loss because an increased amount of binder is added to suppress the self-dusting (cf.
Japanese Patent Kokai Publication No. 16019/1988 and corresponding U.S. Patent No. 4,877,433). In addition, when such a filter material is contacted with a certain chemical such a,s hydrofluoric acid, it creates dust due to deterioratio:a of the glass and the binder.
To sc>lve such drawbacks, an electret filter material made of a synthetic fiber is proposed in Japanese Patent. Kokai Publication No. 53365/1979, but it suffers from deterioration of the electret.
To overcome the above defects, it has been proposed to use a stretched porous film of PTFE as an auxiliary member for the filter material (cf. Japanese Patent Kokai Publication Nos. 16019/1988 and 284614/1990).
However, this proposal uses a porous PTFE film having a pore size of 1 ~.m or larger to prevent an increase in pressure loss.
A theoretical reason to explain why suspended particles having a particle size smaller than the above pore size can still be trapped may be as follows:
There are three mechanisms to remove particles from a fluid using a filter (cf. a brochure of Domnick Hunter Filters Limited).
1. Direct Interception Comparatively large particles are intercepted by microfibers in the filter material and are removed as if they are sieved.
2. Inertial Impaction When the particles pass through winding spaces among the microfibers, they cannot change their direction of movement as quick as the gas so that they collide against the microfibers and adhere thereto.
y 3. Diffusion/Brownian movement Motion of very small particles is controlled by intermolecular forces or static electricity and they spi-rally move in i:he gas, so that their apparent diameters are increased and they adhere to the microfibers as in the case of the inertia7_ collision.
In addition, the suspended particles can be trap-ped by an electric charge trapping mechanism by the electret (cf. Japanese Patent Kokai Publication No. 53365/1979).
However, as unc!erstood from the data of Japanese Patent One of the typical PTFE porous films to be used as the filter material is disclosed in Japanese Patent Publi-Kokai Publication No. 284614/1990 and corresponding EP-A-395 331, the particles having a particle size of 1 ~.m or less cannot be completely removed by this mechanism.
ca non No. 17216/1981 and corresponding U.S. Patent No.
To overcome the above defects, it has been proposed to use a stretched porous film of PTFE as an auxiliary member for the filter material (cf. Japanese Patent Kokai Publication Nos. 16019/1988 and 284614/1990).
However, this proposal uses a porous PTFE film having a pore size of 1 ~.m or larger to prevent an increase in pressure loss.
A theoretical reason to explain why suspended particles having a particle size smaller than the above pore size can still be trapped may be as follows:
There are three mechanisms to remove particles from a fluid using a filter (cf. a brochure of Domnick Hunter Filters Limited).
1. Direct Interception Comparatively large particles are intercepted by microfibers in the filter material and are removed as if they are sieved.
2. Inertial Impaction When the particles pass through winding spaces among the microfibers, they cannot change their direction of movement as quick as the gas so that they collide against the microfibers and adhere thereto.
y 3. Diffusion/Brownian movement Motion of very small particles is controlled by intermolecular forces or static electricity and they spi-rally move in i:he gas, so that their apparent diameters are increased and they adhere to the microfibers as in the case of the inertia7_ collision.
In addition, the suspended particles can be trap-ped by an electric charge trapping mechanism by the electret (cf. Japanese Patent Kokai Publication No. 53365/1979).
However, as unc!erstood from the data of Japanese Patent One of the typical PTFE porous films to be used as the filter material is disclosed in Japanese Patent Publi-Kokai Publication No. 284614/1990 and corresponding EP-A-395 331, the particles having a particle size of 1 ~.m or less cannot be completely removed by this mechanism.
ca non No. 17216/1981 and corresponding U.S. Patent No.
4,187,390.
With this PTFE porous film, the draw ratio should be made large to increase porosity so as to provide a filter material having a small pressure loss.
As a result, pore size is increased. To decrease the pore size, the draw ratio cannot be made large and the produced porou:~ film has a large pressure loss.
One object of the present invention is to provide a PTFE porous film having a small pore size and also small pressure loss.
Another object of the present invention is to provide a filter material having improved ability to trap ultrafine particles.
According to a first aspect of the present invention, there is provided a PTFE porous film which is prepared by stretching a semisintered PTFE material and heating the stretched material at a temperature higher than the melting point of sintered PTFE and has an area ratio of fibrils to nodes of from 99:1 to 75:25, an average fibril diameter of from 0.05 to 0.2 ~,m and a largest node area of not larger than 2 ~.m2 which are determined by image processing of a scanning electron microscopic photograph, and an average pore size of from 0.2 to 0.5 ~.m and a sintering degree of 0.30 to 0.80 calculated according to the following equation:
sintering degree = (~H1 - ~H3) / (~H1 - ~H2) wherein OH1 is heat of fusion of the unsintered polytetrafluoroethylene material, ~H2 is heat of fusion of ,the sintered polytetrafluoroethylene material and ~H3 is heat of fusion of the semisintered polytetrafluoroethylene material.
-4a-According to a second aspect of the present invention, there is provided a PTFE porous film which has a thickness of not larger than about one twentieth of that of a semisintered PTFE material (for example, when thickness of the semisintered material is 100 Vim, thickness of the porous film is 5 ~m or less), average pore size of from 0.2 to 0.5 Vim, an average fibril diameter of from 0.05 to 0.2 ~,m and pressure loss of from 10 to 100 mmH20 when air is passed through the film at a flow rate of 5.3 cm/sec.
', In drawings that illustrated preferred embodiments of the invention:
Fig. .L schematically shows a stretching apparatus used in Examples, Fig. 2 shows crystalline melting curves of the unsintered PTFE material and the sintered PTFE material , Fig. 3 shows a crystalline melting curve of the semisintered PTF'E material , Figs. 4 and 5 are the SEM photographs of the PTFE
porous films prepared in Examples 1 and 2, respectively, Figs. 6 and 7 are images obtained by processing Figs. 4 and 5 ass above, respectively, Figs. 8 and 9 are images of fibrils separated from Figs. 6 and 7, respectively, Figs. 10 and 11 are images of nodes separated from Figs. 6 and 7, respectively Figs. 12 and 13 are the SEM photographs of the commercially available PTFE films A and B, respectively, Figs. 14 and 15 are images of fibrils separated from the images which are obtained by processing Figs. 12 and 13, respectively, Figs. 16 and 17 are images of nodes separated from the images which are obtained by processing Figs. 12 and 13, Figs. 18 to 24 show models of the fibril-node structure of the PTFE porous film, and Fig. 25 schematically shows a stretching and lami-nating apparatus used in Examples 3 and 4.
~~.
With this PTFE porous film, the draw ratio should be made large to increase porosity so as to provide a filter material having a small pressure loss.
As a result, pore size is increased. To decrease the pore size, the draw ratio cannot be made large and the produced porou:~ film has a large pressure loss.
One object of the present invention is to provide a PTFE porous film having a small pore size and also small pressure loss.
Another object of the present invention is to provide a filter material having improved ability to trap ultrafine particles.
According to a first aspect of the present invention, there is provided a PTFE porous film which is prepared by stretching a semisintered PTFE material and heating the stretched material at a temperature higher than the melting point of sintered PTFE and has an area ratio of fibrils to nodes of from 99:1 to 75:25, an average fibril diameter of from 0.05 to 0.2 ~,m and a largest node area of not larger than 2 ~.m2 which are determined by image processing of a scanning electron microscopic photograph, and an average pore size of from 0.2 to 0.5 ~.m and a sintering degree of 0.30 to 0.80 calculated according to the following equation:
sintering degree = (~H1 - ~H3) / (~H1 - ~H2) wherein OH1 is heat of fusion of the unsintered polytetrafluoroethylene material, ~H2 is heat of fusion of ,the sintered polytetrafluoroethylene material and ~H3 is heat of fusion of the semisintered polytetrafluoroethylene material.
-4a-According to a second aspect of the present invention, there is provided a PTFE porous film which has a thickness of not larger than about one twentieth of that of a semisintered PTFE material (for example, when thickness of the semisintered material is 100 Vim, thickness of the porous film is 5 ~m or less), average pore size of from 0.2 to 0.5 Vim, an average fibril diameter of from 0.05 to 0.2 ~,m and pressure loss of from 10 to 100 mmH20 when air is passed through the film at a flow rate of 5.3 cm/sec.
', In drawings that illustrated preferred embodiments of the invention:
Fig. .L schematically shows a stretching apparatus used in Examples, Fig. 2 shows crystalline melting curves of the unsintered PTFE material and the sintered PTFE material , Fig. 3 shows a crystalline melting curve of the semisintered PTF'E material , Figs. 4 and 5 are the SEM photographs of the PTFE
porous films prepared in Examples 1 and 2, respectively, Figs. 6 and 7 are images obtained by processing Figs. 4 and 5 ass above, respectively, Figs. 8 and 9 are images of fibrils separated from Figs. 6 and 7, respectively, Figs. 10 and 11 are images of nodes separated from Figs. 6 and 7, respectively Figs. 12 and 13 are the SEM photographs of the commercially available PTFE films A and B, respectively, Figs. 14 and 15 are images of fibrils separated from the images which are obtained by processing Figs. 12 and 13, respectively, Figs. 16 and 17 are images of nodes separated from the images which are obtained by processing Figs. 12 and 13, Figs. 18 to 24 show models of the fibril-node structure of the PTFE porous film, and Fig. 25 schematically shows a stretching and lami-nating apparatus used in Examples 3 and 4.
~~.
.~~ , The PTFE porous film of the present invention may be used as such or reinforced by laminating a separate rein-forcing material having a low pressure loss. The laminated PTFE porous film has improved handleability. The laminated PTFE porous film can be folded in a pleat form and used as a filter for trapping ultrafine particles.
As the reinforcing material, nonwoven fabric, woven fabric, mesh or other porous materials may be used.
The reinforcing material can be made from various raw mate-rials such as polyolefin (e. g. polyethylene, polypropylene, etc.), polyamide, polyester, aramid or a composite such as a non-woven fabric of a fiber having a core/shell struc-ture, a two-layer non-woven fabric of a low melting point material and a high melting point material, a fluororesin (e. g. tetrafluoroethylene/perfluoroalkyl vinyl ether copoly-mer) (PFA), tetrafluoroethylene/hexafluoropropylene copoly-mer (FEP), polytetrafluoroethylene (PTFE) etc.) and the like. Among them, the non-woven fabric of the fiber having the core/shell ;structure and the two-layer non-woven fabric of the low melting point material and the high melting point material are preferred since they do not shrink during lami-nation. The laminated film with such reinforcing material is easily processed in the form of a HEPA (high efficiency particulate air) filter and can increase the number of fol-ding pitches when it is processed as a filter element.
n _ 7 _ The structure of the lamination is not limited. For example, on one or both surfaces of the reinforcing mate-rial, the PTFE porous films) of the present invention is laminated, or t:he PTFE porous material is sandwiched between a pair of reinforcing materials.
The PTFE porous film and the reinforcing material may be laminated by any conventional method, for example, thermocompression bonding with melting a part of the reinforcing material or using, as an adhesive, a powder of polyethylene, polyester. or PFA, or a hot-melt resin.
In view of the particle removing mechanisms as explained above, it is necessary to prevent desorption of the particles which once adhere to the fiber of the filter or shield the passing through particles so as to trap the particles surely. To this end, the filter material having a pore size smaller than the particle size of the particles to be surely trapped should be used, and therefore the PTFE
porous material having a small average pore size is prefer-red.
The smaller the film thickness, the better, since the pressure loss is proportional to film thickness when the pore d_~ameter and the porosity of the filter mate-rial are the sarne.
Even if the pressure loss, pore size, porosity and film thickness of the filter material are the same, abi-lity to trap the' particles varies with the materials.
f'.w _ g _ Theoretically, it is preferred to use thin fibers having a diameter of 0.5 ~m or less and decrease the amount of binder, namely decrease the amount of material other than the fiber (cf. The 52 Year Preprint of Emi Jun of the Chemical Engineering Society).
The PTFE porous film of the present invention satisfies such conditions.
The PTFE porous film of the present invention will be explained in more detail together with its production process.
An unstretched material of PTFE film to be used as a raw material in the present invention is a semisintered material of PTFE which is disclosed in Japanese Patent Kokai Publication No. 152825/1984 and corresponding to U.S. Patent No. 4,596,837).
The s~~misintered PTFE material is biaxially stret-ched at an area draw ratio of at least 50, preferably at least 100, more preferably at least 250 and then sintered, and the sintered PTFE porous film has a very unique film structure and comprises fibers including substantially no nodes.
The.PTFE porous film thus produced has a very small average pore size of, for example, from 0.2 to 0.5 um, and its thickness is reduced to about one twentieth to about one hundredth of the thickness of the unstretched semisintered PTF?E material.
Such parameters are suitable to ensure that the air filter material maintains a highly clear space in which a micro-pattern is formed on a semiconductor.
The F~TFE porous film having the above structure has not been produced by a conventional process. For example, Japanese Patent Publication No. 17216/1981 descri-bes, in column 11, line 23 et seq, that "Fig. 1 shows an elongation effect in an uniaxial direction. By biaxial stretching or stretching in all directions, microfibers are formed in those directions, so that a cobweb structure or a cross linked structure is formed and, in association there-with, the strength is increased. Since the number and sizes of spaces between the nodes and the microfibers of the poly-mer increase, the porosity increases also. This means that an increase of the draw ratio results in only an increase of the pore size.
The pressure loss decreases as the pore size inc-reases or the film thikcness decreases. To produce an air filter having a small pore size and low pressure loss, a thin PTFE film :i.s used. In the conventional process of Japanese Patf~nt Publication No. 17216/1981, an increase of the draw ratio does not lead to a decrease of the width and thickness. When the draw ratio is significantly increased, the pore size is enlarged. Therefore, the film thickness before stretching should be made thin and the film should be stretched at a small draw ratio.
A
,,.., - 10 -However, the thickness of the technically usable film before stretching is at most 30 to 50 um. By taking quality and yield of the produced film into consideration, the thickness of the film before stretch ing is about 100 um.
One of the characteristics of the present inven-tion is that the final PTFE porous film can be prepared from a non-stretched film having a thickness of about 100 um.
General ranges and preferred r anges of the para-meters of the present invention are as f ollows:
-General range Preferred range Sintering degree: 0.30-0.80 0.35-0.70 Draw ratio: in .MD 4-30 5-25 in 'rD 10-100 15-70 total 50-1000 75-850 When the total draw ratio is 250 or larger, the sintering degree is preferably from 0.35 to 0.48.
General range Preferred range Average pore sie: 0.2-0.5 um 0.2-0.4 um Film thickness: 0.5-15 um 0.5-10 um Area ratio of fibrils to nodes: 99/1-75/25 99/1-85/15 Average fibril diameter: 0.05-0.2 um 0.05-0.2 um Largest area of node: <2 um2 0.05-1 um2 Pressure loss: 10-100 mmI~20 10-70 m_mH20 The sintering degree is defined in the Examples.
The P'rFE porous film of the present invention can be used as an a:ir filter. In addition, when a liquid is vaporized through the PTFE porous film of the present inven-tion as a partii~ion film, a clear gas containing no impurity particles in thf~ liquid can be obtained. An example of such an application is a separation film of a clean moistening appa-ratus.
According to the present invention, the very thin PTFE porous filrn can be mass produced and the PTFE porous film of the present invention can be used in an application where water repellency or gas permeability is required.
The present invention will be explained in further detail by the following Examples.
Examp='_e 1 An unstretched unsintered PTFE film having a thickness of 100 um, which was prepared from PTFE fine pow-der (Polyflon (t:rademark) Fine Powder F-104 manufactured by Daikin Industries, Ltd.), was heated in an oven kept at 339°C for 50 seconds to obtain a continuous semisintered film having a sintering degree of 0.50.
The se~misintered film was cut to a sample of about 9 cm square, and its four sides were clamped with clips of an apparatus wh=_ch can biaxially stretch a film simultane-ously or successively (manufactured by Iwamoto Manufacturing Co., Ltd.), heated at an atmosphere temperature of 320°C for A
t...
15 minutes and stretched at a rate of 100 %/sec. in a longi-tudinal direction of the film (referred to as "MD" direc-tion) at a draw ratio of 5.
Then, the sample was continuously stretched in a width direction of the film (referred to as "TD" direction) at a draw ratio of 15 while fixing the length in the MD
direction to obtain a porous film stretched at a total draw ratio (area draw ratio) of 75.
This stretched film was set on a frame to pre-venting shrinkage and heat_set in an oven kept at 350°C for 3 minutes.
Example 2 The same semisintered film having a sintering degree of 0.5 as used in Example 1 was stretched at a draw ratio of 8 in the MD direction and at the draw ratio of 25 in the TD direction (total draw ratio of 200) in the same manner as in Example 1 to obtain a stretched PTFE porous film.
This ,porous film was heat set at 350°C for 3 minu-tes in the same manner as in Example 1.
Example 3 An unstretched unsintered PTFE film having a thic-kness of 100 um was prepared from the same PTFE fine powder as used in Example 1 by paste extrusion, calendering with rolls and lubricant drying according to a conventional method, and heated in an oven kept at 338°C for 45 seconds to obtain a continuous semisintered film having a sinte-ring degree of 0.40. Before this heating step, the film had a width of 215 mm and a specific gravity of 1.55 g/cm3, and after this heating step, the film had a width of 200 mm and a specific gravity of 2.25 g/cm3. However, the thicknesses before and after heating were substantially the same.
This aemisintered film was stretched in the longi-tudinal direction at a draw ratio of 20 using the apparatus shown in Fig. 1.
The si~retching conditions in the longitudinal direction are as follows:
Rolls 3 and 4: Feeding speed: 0.5 m/min.
Temperature: room temperature Film width: 200 mm Roll Ei: Peripheral speed: 4 m/min.
Temperature: 300°C
Roll ;: Peripheral speed: 10 m/min.
Temperature: 300°C
Roll 1.0: Peripheral speed: 10 m/min.
Temperature: 25°C
Winding roll 2: Winding speed: 10 m/min.
Temperature: Room temperature Film width: 145 mm Distance between peripheries of rolls 6 and 7: 5 mm An area draw ratio in the longitudinal direction was calculated to be 14.5.
Then, the longitudinally stretched film was stret ched at a draw ratio of about 34 and heat set using an appa ratus of Fig. 25 which can successively clamp both edges of the film with clips.
In Fig. 25, numerals stand for the following parts:
13: Film feeding roll 14: Feed control mechanism 15: Preheating oven 16: Oven for stretching in a width direction 17: Heat setting oven 18, 19: Laminating rolls (19: heating roll) 20: Winding control mechanism 21: Winding roll 22, 23: Drums for laminating non-woven fabrics In the above step, the stretching and heat setting conditions are .as follows:
Film feeding speed: 3 m/min.
Temp. of preheating oven: 305°C
Temp. of oven for stret~~hing in width direction: 320°C
Temp. of heat setting oven: 350°C
The total area draw ratio was calculated to be about 490.
A
Exam~~le 4 On both surfaces of the film stretched in the width direction, non-woven fabrics were laminated using the apparatus of Fig. 25.
The laminating conditions are as follows:
Upper non-woven fabric: ELEVES T 1003 WDO *
(manufactured by UNITIKA) Lower non-woven fabric: Melfit BT 030 E*
(manufactured by UNISEL) Temp. of heating-.roll 19: 150°C
The average pressure loss of the laminated PTFE
porous film was 25 mmHzO. The pressure loss was measured as follows:
Each edge of the stretched film was cut at an equal distance to obtain a film having a width of 800 mm, and the pressure loss was measured at four points which were present on the came width line at equal intervals. The maximum pressure loss was 27 mmH20 and the minimum pressure loss was 23 mmH,20.
Reference Example The same semisintered PTFE film as used in Example 1 was stretched with the apparatus of Fig. 1. That is, from the feeding roll 1, the semisintered PTFE film was fed to the rolls 6, 7 through the rolls 3, 4, 5, whereby the film was stretched in the MD direction at a draw ratio of 6.
*Trade Mark The stretched film was then passed through the rolls 8, 9, the heat setting roll 10, the cooling roll 11 and the roll 12 and wound on the winding roll 2.
The stretching conditions are as follows:
Roll fi: Roll surface temperature: 300°C
Peripheral speed: 1 m/min.
Roll ;: Roll surface temperature: 300°C
Peripheral speed: 6 m/min.
Distance between peripheries of rolls 6 and 7: 5 mm Roll 1.0: Roll surface temperature: 300°C
Peripheral speed: synchronous to roll 7 The stretched film was cut to a length of 1 m and a width of 15 cm and the cut film was stretched in the TD
direction without fixing the width at a draw ratio of 4 and heat set at 350°C for 3 minutes. In this stretched film, no node was found according to the definition of the present invention.
With the films produced in Examples 1, 2 and 3 and the Reference Example and two commercially available PTFE films having a pore size of 0.1 um (A: a PTFE porous film assem-bled in FLUOROGURAD*TP Cartridge 0.1 ym manufactured by Millipore) B: T 300 A 293-D PTFE membrane filter manufac-tured by Advantec Toyo) as Comparative Examples, an average pore size, a film thickness, an area ratio of fibrils to nodes, an average fibril diameter, the largest node area and w% *Trade Mark ,,~
a pressure loss were measured as described below. The results are shown in the Table.
Table Exam- Film Av. Area Average Largest Pressure ple thick- pore ratio of fibril node loss No. ness size fibrils diameter area (mmH20) (um) (um) to nodes (um) (um2) 1 4.5 0.26 90/10 0.15 1.2 65 2 1.0 0.28 95/5 0.14 0.38 45 3 0.8 0.30 96/4 0.14 0.36 15 Ref. 50 0.27 0.27 1300 Com.
Ex.
A 70 0.28 65/35 0.15 7.5 1290 B 70 2.90 55 From the results of the Table, it is understood that, though the PTFE porous films of the present invention have substantia:Lly the same average pore size as those of commercially available film A and Reference Example, they have much smallE~r pressure loss than the latter and that, though the PTFE porous films of Examples 1 and 2 have subs-tantially the same pressure loss as that of the commercially available film B, they have much larger average pore size than the latter,. In addition, it is understood that, when the film is stretched at the area draw ratio of about 500 as in Example 3, the pressure loss can be further decreased while the average pore size is at the same level.
The PTFE porous films of the Examples have a larger area ratio of fibrils to nodes than the commercially available film A. The PTFE porous films of Examples have a smaller average fibril diameter than that of Reference E~s:ample. The largest node area of the PTFE
porous film of the present invention is much smaller than that of commercially available film A.
The properties in the Table are measured as follows:
Average pore size A mean flow pore size measured according to ASTM
F-316-86 is used as an average pore size. Herein, the mean flow pore size is measured using Coulter Porometer (manufac-tured by Coulter Electronics, UK).
Film thickness Using 1D-110 MH type film thickness meter (manu-facture by Mitsutoyo Co., Ltd.), a total thickness of lami-nated file films is measured and the measured value is divi-ded by 5 to obtain a film thickness of one film.
Pressure loss A PTFE porous film is cut to a round shape of 47 mm in diameter .and set on a filter holder having an effec-tive transmission area of 12.6 cm2. The entrance side is pressurized at ~0.4 kg/cmz with air and transmission rate through the porous film is controlled to 5.3 cm/sec. by adjusting the f:Low rate of the air from-the exit side by a f flow meter (mar..ufactured by Ueshima Manufacturing Co., Ltd.). Under such conditions, pressure loss is measured with a manometer.
Sintering degree Sintering degree of a semisintered PTFE material is defined as follows:
From an unsintered PTFE material, a sample of 3.0~0.1 mg is weighed, and with this sample, a crystalline melting curve is measured. From a semisintered PTFE mate-rial, a sample of 3.0~0.1 mg is weighed, and with this sample, a crystalline melting curve is measured.
The crystalline melting curve is recorded using a differential scanning calorimeter (hereinafter referred to as "DSC") such as DSC-50*manufactured by Shimadzu.
The sample of the unsintered PTFE material is charged in an aluminum pan of a DSC and heat of fusion of the unsintered PTFE material and that of a sintered PTFE
material are measured by the following procedures:
(1) The sample is heated at a heating rate of 50°C/min. up to 250°C and then at a heating rate of 10°C/min. from 250°C to 380°C. An example of a crystalline melting curve recorded in this heating step is shown in Fig.
2, Curve A. The temperature at which an endothermic peak appears is defined as "melting point of the unsintered PTFE material" or "melting point of PTFE fine powder".
*Trade Mark i';t.
(2) Immediately after the temperature reaches 380°C, the sample is cooled at a cooling rate of 10°C/min.
down to 250°C.
(3) Then, the sample is again heated up to 380°C
at a heating rate of 10°C/min.
An example of a crystalline melting curve recorded in the heating step (3) is shown in Fig. 2, Curve B.
The temperature at which an endothermic peak appears is defined as "melting point of the sintered PTFE mate-rial" .
Next, a crystalline melting curve of the semisin-tered PTFE material is recorded in the same manner as step (1). An e:~ample of a crystalline melting curve in this step is shown in Fig. 3.
'C'r~e heat of fusion of each of the unsintered PTFE
material (0H1 oi= Fig. 1), the sintered PTFE material (~H2 of Fig. 1) and the semisintered PTFE material (oH3 of Fig. 2) is proportional to an area surrounded by the crystalline melting curve and a base line, and the heat of fusion is automatically calculated by DSC-SO of Shimadzu.
Then, sintering degree is calculated according to the following equation:
Sintering degree = (0H1 - ~H3)/(oHl nH2) wherein oHl is heat of fusion of the unsintered PTFE mate-rial, flH2 is heat of fusion of the sintered PTFE material and eH3 is heat of fusion of the semisintered PTFE mate-rial.
A detailed explanation of the semisintered PTFE
is found in Japanese Patent Kokai Publication No~
material nd corresponding to U.S. Patent No. 4,596,837.
152825/1984 a Image analv area ratio of fibrils to nodes, the average The eter anti the largest nodes area are measured as fibril dram follows:
to raph of a surface of a PTFE porous film is A pho 9 a scanning electron microscope (Hitachi S-400, .
taken with 'th Hitachi H-1030) (SEM photograPh~ Ma9nifi-vaporization wi to 5000 times). This photograph is scanned cation: 1000 ith an image processing apparatus (hardware: TV Image w VIP-4100 II*manufactured by Nippon Avionics Co., Processor T
of software: TV Image Processor Image Command Ltd.; contr * Latock System Engineering Co., Ltd.) to 4198 supplied bY .
fibrils and the nodes to obtain an image of the separate the hat of the nodes. By processing the image of fibrils and t the largest node area is obtained, and by proces-the nodes.
of the fibrils. an average fibril diameter is sing the image ratio of the total area to half of the total obtained peripheral length).
.area ratio of the fibrils to the nodes calcu-The i.o of the total area of the fibril image and lated as a rat that of the node image~
4 and 5 are the SEM photographs of the PTFE
Figs.
'lms prepared in Examples 1 and 2, respectively.
porous fl *Trade Mark Figs. 6 and 7 are images obtained by processing Figs. 4 and 5 as above, respectively.
Figs. 8 and 9 are images of fibrils separated from Figs. 6 and 7, respectively.
Figs. 10 and 11 are images of nodes separated from Figs. 6 and 7, respectively.
Figs. 12 and 13 are the SEM photographs of the commercially available PTFE films A and B, respectively.
Figs. 14 and 15 are images of fibrils separated from the images which are obtained by processing Figs. 12 and 13, respectively.
Figs. 16 and 17 are images of nodes separated from the images which. are obtained by processing Figs. 12 and 13.
Definition of nodes Herein, the nodes satisfy one of the following properties:
(i) A block to which plural fibrils are connec-ted (dotted areas in Fig. 18) (ii) A block which is larger than the diameter of a fibril connected to the block (hatched areas in Figs. 21 and 22) (iii') A primary particle or agglomerated primary particles from which fibrils radially extend (hatched areas in Figs. 19, 22 and 23) k:
Fig. 24 is an example of a structure which is not regarded as a node. In Fig. 24, the fibrils are branched out, but the size of the branched area is the same as the diameter of the fibril. This branched area is not regarded as a node in the present invention.
n
As the reinforcing material, nonwoven fabric, woven fabric, mesh or other porous materials may be used.
The reinforcing material can be made from various raw mate-rials such as polyolefin (e. g. polyethylene, polypropylene, etc.), polyamide, polyester, aramid or a composite such as a non-woven fabric of a fiber having a core/shell struc-ture, a two-layer non-woven fabric of a low melting point material and a high melting point material, a fluororesin (e. g. tetrafluoroethylene/perfluoroalkyl vinyl ether copoly-mer) (PFA), tetrafluoroethylene/hexafluoropropylene copoly-mer (FEP), polytetrafluoroethylene (PTFE) etc.) and the like. Among them, the non-woven fabric of the fiber having the core/shell ;structure and the two-layer non-woven fabric of the low melting point material and the high melting point material are preferred since they do not shrink during lami-nation. The laminated film with such reinforcing material is easily processed in the form of a HEPA (high efficiency particulate air) filter and can increase the number of fol-ding pitches when it is processed as a filter element.
n _ 7 _ The structure of the lamination is not limited. For example, on one or both surfaces of the reinforcing mate-rial, the PTFE porous films) of the present invention is laminated, or t:he PTFE porous material is sandwiched between a pair of reinforcing materials.
The PTFE porous film and the reinforcing material may be laminated by any conventional method, for example, thermocompression bonding with melting a part of the reinforcing material or using, as an adhesive, a powder of polyethylene, polyester. or PFA, or a hot-melt resin.
In view of the particle removing mechanisms as explained above, it is necessary to prevent desorption of the particles which once adhere to the fiber of the filter or shield the passing through particles so as to trap the particles surely. To this end, the filter material having a pore size smaller than the particle size of the particles to be surely trapped should be used, and therefore the PTFE
porous material having a small average pore size is prefer-red.
The smaller the film thickness, the better, since the pressure loss is proportional to film thickness when the pore d_~ameter and the porosity of the filter mate-rial are the sarne.
Even if the pressure loss, pore size, porosity and film thickness of the filter material are the same, abi-lity to trap the' particles varies with the materials.
f'.w _ g _ Theoretically, it is preferred to use thin fibers having a diameter of 0.5 ~m or less and decrease the amount of binder, namely decrease the amount of material other than the fiber (cf. The 52 Year Preprint of Emi Jun of the Chemical Engineering Society).
The PTFE porous film of the present invention satisfies such conditions.
The PTFE porous film of the present invention will be explained in more detail together with its production process.
An unstretched material of PTFE film to be used as a raw material in the present invention is a semisintered material of PTFE which is disclosed in Japanese Patent Kokai Publication No. 152825/1984 and corresponding to U.S. Patent No. 4,596,837).
The s~~misintered PTFE material is biaxially stret-ched at an area draw ratio of at least 50, preferably at least 100, more preferably at least 250 and then sintered, and the sintered PTFE porous film has a very unique film structure and comprises fibers including substantially no nodes.
The.PTFE porous film thus produced has a very small average pore size of, for example, from 0.2 to 0.5 um, and its thickness is reduced to about one twentieth to about one hundredth of the thickness of the unstretched semisintered PTF?E material.
Such parameters are suitable to ensure that the air filter material maintains a highly clear space in which a micro-pattern is formed on a semiconductor.
The F~TFE porous film having the above structure has not been produced by a conventional process. For example, Japanese Patent Publication No. 17216/1981 descri-bes, in column 11, line 23 et seq, that "Fig. 1 shows an elongation effect in an uniaxial direction. By biaxial stretching or stretching in all directions, microfibers are formed in those directions, so that a cobweb structure or a cross linked structure is formed and, in association there-with, the strength is increased. Since the number and sizes of spaces between the nodes and the microfibers of the poly-mer increase, the porosity increases also. This means that an increase of the draw ratio results in only an increase of the pore size.
The pressure loss decreases as the pore size inc-reases or the film thikcness decreases. To produce an air filter having a small pore size and low pressure loss, a thin PTFE film :i.s used. In the conventional process of Japanese Patf~nt Publication No. 17216/1981, an increase of the draw ratio does not lead to a decrease of the width and thickness. When the draw ratio is significantly increased, the pore size is enlarged. Therefore, the film thickness before stretching should be made thin and the film should be stretched at a small draw ratio.
A
,,.., - 10 -However, the thickness of the technically usable film before stretching is at most 30 to 50 um. By taking quality and yield of the produced film into consideration, the thickness of the film before stretch ing is about 100 um.
One of the characteristics of the present inven-tion is that the final PTFE porous film can be prepared from a non-stretched film having a thickness of about 100 um.
General ranges and preferred r anges of the para-meters of the present invention are as f ollows:
-General range Preferred range Sintering degree: 0.30-0.80 0.35-0.70 Draw ratio: in .MD 4-30 5-25 in 'rD 10-100 15-70 total 50-1000 75-850 When the total draw ratio is 250 or larger, the sintering degree is preferably from 0.35 to 0.48.
General range Preferred range Average pore sie: 0.2-0.5 um 0.2-0.4 um Film thickness: 0.5-15 um 0.5-10 um Area ratio of fibrils to nodes: 99/1-75/25 99/1-85/15 Average fibril diameter: 0.05-0.2 um 0.05-0.2 um Largest area of node: <2 um2 0.05-1 um2 Pressure loss: 10-100 mmI~20 10-70 m_mH20 The sintering degree is defined in the Examples.
The P'rFE porous film of the present invention can be used as an a:ir filter. In addition, when a liquid is vaporized through the PTFE porous film of the present inven-tion as a partii~ion film, a clear gas containing no impurity particles in thf~ liquid can be obtained. An example of such an application is a separation film of a clean moistening appa-ratus.
According to the present invention, the very thin PTFE porous filrn can be mass produced and the PTFE porous film of the present invention can be used in an application where water repellency or gas permeability is required.
The present invention will be explained in further detail by the following Examples.
Examp='_e 1 An unstretched unsintered PTFE film having a thickness of 100 um, which was prepared from PTFE fine pow-der (Polyflon (t:rademark) Fine Powder F-104 manufactured by Daikin Industries, Ltd.), was heated in an oven kept at 339°C for 50 seconds to obtain a continuous semisintered film having a sintering degree of 0.50.
The se~misintered film was cut to a sample of about 9 cm square, and its four sides were clamped with clips of an apparatus wh=_ch can biaxially stretch a film simultane-ously or successively (manufactured by Iwamoto Manufacturing Co., Ltd.), heated at an atmosphere temperature of 320°C for A
t...
15 minutes and stretched at a rate of 100 %/sec. in a longi-tudinal direction of the film (referred to as "MD" direc-tion) at a draw ratio of 5.
Then, the sample was continuously stretched in a width direction of the film (referred to as "TD" direction) at a draw ratio of 15 while fixing the length in the MD
direction to obtain a porous film stretched at a total draw ratio (area draw ratio) of 75.
This stretched film was set on a frame to pre-venting shrinkage and heat_set in an oven kept at 350°C for 3 minutes.
Example 2 The same semisintered film having a sintering degree of 0.5 as used in Example 1 was stretched at a draw ratio of 8 in the MD direction and at the draw ratio of 25 in the TD direction (total draw ratio of 200) in the same manner as in Example 1 to obtain a stretched PTFE porous film.
This ,porous film was heat set at 350°C for 3 minu-tes in the same manner as in Example 1.
Example 3 An unstretched unsintered PTFE film having a thic-kness of 100 um was prepared from the same PTFE fine powder as used in Example 1 by paste extrusion, calendering with rolls and lubricant drying according to a conventional method, and heated in an oven kept at 338°C for 45 seconds to obtain a continuous semisintered film having a sinte-ring degree of 0.40. Before this heating step, the film had a width of 215 mm and a specific gravity of 1.55 g/cm3, and after this heating step, the film had a width of 200 mm and a specific gravity of 2.25 g/cm3. However, the thicknesses before and after heating were substantially the same.
This aemisintered film was stretched in the longi-tudinal direction at a draw ratio of 20 using the apparatus shown in Fig. 1.
The si~retching conditions in the longitudinal direction are as follows:
Rolls 3 and 4: Feeding speed: 0.5 m/min.
Temperature: room temperature Film width: 200 mm Roll Ei: Peripheral speed: 4 m/min.
Temperature: 300°C
Roll ;: Peripheral speed: 10 m/min.
Temperature: 300°C
Roll 1.0: Peripheral speed: 10 m/min.
Temperature: 25°C
Winding roll 2: Winding speed: 10 m/min.
Temperature: Room temperature Film width: 145 mm Distance between peripheries of rolls 6 and 7: 5 mm An area draw ratio in the longitudinal direction was calculated to be 14.5.
Then, the longitudinally stretched film was stret ched at a draw ratio of about 34 and heat set using an appa ratus of Fig. 25 which can successively clamp both edges of the film with clips.
In Fig. 25, numerals stand for the following parts:
13: Film feeding roll 14: Feed control mechanism 15: Preheating oven 16: Oven for stretching in a width direction 17: Heat setting oven 18, 19: Laminating rolls (19: heating roll) 20: Winding control mechanism 21: Winding roll 22, 23: Drums for laminating non-woven fabrics In the above step, the stretching and heat setting conditions are .as follows:
Film feeding speed: 3 m/min.
Temp. of preheating oven: 305°C
Temp. of oven for stret~~hing in width direction: 320°C
Temp. of heat setting oven: 350°C
The total area draw ratio was calculated to be about 490.
A
Exam~~le 4 On both surfaces of the film stretched in the width direction, non-woven fabrics were laminated using the apparatus of Fig. 25.
The laminating conditions are as follows:
Upper non-woven fabric: ELEVES T 1003 WDO *
(manufactured by UNITIKA) Lower non-woven fabric: Melfit BT 030 E*
(manufactured by UNISEL) Temp. of heating-.roll 19: 150°C
The average pressure loss of the laminated PTFE
porous film was 25 mmHzO. The pressure loss was measured as follows:
Each edge of the stretched film was cut at an equal distance to obtain a film having a width of 800 mm, and the pressure loss was measured at four points which were present on the came width line at equal intervals. The maximum pressure loss was 27 mmH20 and the minimum pressure loss was 23 mmH,20.
Reference Example The same semisintered PTFE film as used in Example 1 was stretched with the apparatus of Fig. 1. That is, from the feeding roll 1, the semisintered PTFE film was fed to the rolls 6, 7 through the rolls 3, 4, 5, whereby the film was stretched in the MD direction at a draw ratio of 6.
*Trade Mark The stretched film was then passed through the rolls 8, 9, the heat setting roll 10, the cooling roll 11 and the roll 12 and wound on the winding roll 2.
The stretching conditions are as follows:
Roll fi: Roll surface temperature: 300°C
Peripheral speed: 1 m/min.
Roll ;: Roll surface temperature: 300°C
Peripheral speed: 6 m/min.
Distance between peripheries of rolls 6 and 7: 5 mm Roll 1.0: Roll surface temperature: 300°C
Peripheral speed: synchronous to roll 7 The stretched film was cut to a length of 1 m and a width of 15 cm and the cut film was stretched in the TD
direction without fixing the width at a draw ratio of 4 and heat set at 350°C for 3 minutes. In this stretched film, no node was found according to the definition of the present invention.
With the films produced in Examples 1, 2 and 3 and the Reference Example and two commercially available PTFE films having a pore size of 0.1 um (A: a PTFE porous film assem-bled in FLUOROGURAD*TP Cartridge 0.1 ym manufactured by Millipore) B: T 300 A 293-D PTFE membrane filter manufac-tured by Advantec Toyo) as Comparative Examples, an average pore size, a film thickness, an area ratio of fibrils to nodes, an average fibril diameter, the largest node area and w% *Trade Mark ,,~
a pressure loss were measured as described below. The results are shown in the Table.
Table Exam- Film Av. Area Average Largest Pressure ple thick- pore ratio of fibril node loss No. ness size fibrils diameter area (mmH20) (um) (um) to nodes (um) (um2) 1 4.5 0.26 90/10 0.15 1.2 65 2 1.0 0.28 95/5 0.14 0.38 45 3 0.8 0.30 96/4 0.14 0.36 15 Ref. 50 0.27 0.27 1300 Com.
Ex.
A 70 0.28 65/35 0.15 7.5 1290 B 70 2.90 55 From the results of the Table, it is understood that, though the PTFE porous films of the present invention have substantia:Lly the same average pore size as those of commercially available film A and Reference Example, they have much smallE~r pressure loss than the latter and that, though the PTFE porous films of Examples 1 and 2 have subs-tantially the same pressure loss as that of the commercially available film B, they have much larger average pore size than the latter,. In addition, it is understood that, when the film is stretched at the area draw ratio of about 500 as in Example 3, the pressure loss can be further decreased while the average pore size is at the same level.
The PTFE porous films of the Examples have a larger area ratio of fibrils to nodes than the commercially available film A. The PTFE porous films of Examples have a smaller average fibril diameter than that of Reference E~s:ample. The largest node area of the PTFE
porous film of the present invention is much smaller than that of commercially available film A.
The properties in the Table are measured as follows:
Average pore size A mean flow pore size measured according to ASTM
F-316-86 is used as an average pore size. Herein, the mean flow pore size is measured using Coulter Porometer (manufac-tured by Coulter Electronics, UK).
Film thickness Using 1D-110 MH type film thickness meter (manu-facture by Mitsutoyo Co., Ltd.), a total thickness of lami-nated file films is measured and the measured value is divi-ded by 5 to obtain a film thickness of one film.
Pressure loss A PTFE porous film is cut to a round shape of 47 mm in diameter .and set on a filter holder having an effec-tive transmission area of 12.6 cm2. The entrance side is pressurized at ~0.4 kg/cmz with air and transmission rate through the porous film is controlled to 5.3 cm/sec. by adjusting the f:Low rate of the air from-the exit side by a f flow meter (mar..ufactured by Ueshima Manufacturing Co., Ltd.). Under such conditions, pressure loss is measured with a manometer.
Sintering degree Sintering degree of a semisintered PTFE material is defined as follows:
From an unsintered PTFE material, a sample of 3.0~0.1 mg is weighed, and with this sample, a crystalline melting curve is measured. From a semisintered PTFE mate-rial, a sample of 3.0~0.1 mg is weighed, and with this sample, a crystalline melting curve is measured.
The crystalline melting curve is recorded using a differential scanning calorimeter (hereinafter referred to as "DSC") such as DSC-50*manufactured by Shimadzu.
The sample of the unsintered PTFE material is charged in an aluminum pan of a DSC and heat of fusion of the unsintered PTFE material and that of a sintered PTFE
material are measured by the following procedures:
(1) The sample is heated at a heating rate of 50°C/min. up to 250°C and then at a heating rate of 10°C/min. from 250°C to 380°C. An example of a crystalline melting curve recorded in this heating step is shown in Fig.
2, Curve A. The temperature at which an endothermic peak appears is defined as "melting point of the unsintered PTFE material" or "melting point of PTFE fine powder".
*Trade Mark i';t.
(2) Immediately after the temperature reaches 380°C, the sample is cooled at a cooling rate of 10°C/min.
down to 250°C.
(3) Then, the sample is again heated up to 380°C
at a heating rate of 10°C/min.
An example of a crystalline melting curve recorded in the heating step (3) is shown in Fig. 2, Curve B.
The temperature at which an endothermic peak appears is defined as "melting point of the sintered PTFE mate-rial" .
Next, a crystalline melting curve of the semisin-tered PTFE material is recorded in the same manner as step (1). An e:~ample of a crystalline melting curve in this step is shown in Fig. 3.
'C'r~e heat of fusion of each of the unsintered PTFE
material (0H1 oi= Fig. 1), the sintered PTFE material (~H2 of Fig. 1) and the semisintered PTFE material (oH3 of Fig. 2) is proportional to an area surrounded by the crystalline melting curve and a base line, and the heat of fusion is automatically calculated by DSC-SO of Shimadzu.
Then, sintering degree is calculated according to the following equation:
Sintering degree = (0H1 - ~H3)/(oHl nH2) wherein oHl is heat of fusion of the unsintered PTFE mate-rial, flH2 is heat of fusion of the sintered PTFE material and eH3 is heat of fusion of the semisintered PTFE mate-rial.
A detailed explanation of the semisintered PTFE
is found in Japanese Patent Kokai Publication No~
material nd corresponding to U.S. Patent No. 4,596,837.
152825/1984 a Image analv area ratio of fibrils to nodes, the average The eter anti the largest nodes area are measured as fibril dram follows:
to raph of a surface of a PTFE porous film is A pho 9 a scanning electron microscope (Hitachi S-400, .
taken with 'th Hitachi H-1030) (SEM photograPh~ Ma9nifi-vaporization wi to 5000 times). This photograph is scanned cation: 1000 ith an image processing apparatus (hardware: TV Image w VIP-4100 II*manufactured by Nippon Avionics Co., Processor T
of software: TV Image Processor Image Command Ltd.; contr * Latock System Engineering Co., Ltd.) to 4198 supplied bY .
fibrils and the nodes to obtain an image of the separate the hat of the nodes. By processing the image of fibrils and t the largest node area is obtained, and by proces-the nodes.
of the fibrils. an average fibril diameter is sing the image ratio of the total area to half of the total obtained peripheral length).
.area ratio of the fibrils to the nodes calcu-The i.o of the total area of the fibril image and lated as a rat that of the node image~
4 and 5 are the SEM photographs of the PTFE
Figs.
'lms prepared in Examples 1 and 2, respectively.
porous fl *Trade Mark Figs. 6 and 7 are images obtained by processing Figs. 4 and 5 as above, respectively.
Figs. 8 and 9 are images of fibrils separated from Figs. 6 and 7, respectively.
Figs. 10 and 11 are images of nodes separated from Figs. 6 and 7, respectively.
Figs. 12 and 13 are the SEM photographs of the commercially available PTFE films A and B, respectively.
Figs. 14 and 15 are images of fibrils separated from the images which are obtained by processing Figs. 12 and 13, respectively.
Figs. 16 and 17 are images of nodes separated from the images which. are obtained by processing Figs. 12 and 13.
Definition of nodes Herein, the nodes satisfy one of the following properties:
(i) A block to which plural fibrils are connec-ted (dotted areas in Fig. 18) (ii) A block which is larger than the diameter of a fibril connected to the block (hatched areas in Figs. 21 and 22) (iii') A primary particle or agglomerated primary particles from which fibrils radially extend (hatched areas in Figs. 19, 22 and 23) k:
Fig. 24 is an example of a structure which is not regarded as a node. In Fig. 24, the fibrils are branched out, but the size of the branched area is the same as the diameter of the fibril. This branched area is not regarded as a node in the present invention.
n
Claims (9)
1. A polytetrafluoroethylene porous film which is prepared by stretching a semisintered polytetrafluoroethylene material and heating the stretched material at a temperature higher than the melting point of sintered polytetrafluoroethylene and has an area ratio of fibrils to nodes of from 99:1 to 75:25, an average fibril diameter of from 0.05 to 0.2 µm and a largest node area of not larger than 2 µm2 which are determined by image processing of a scanning electron microscopic photograph, an average pore size of from 0.2 to 0.5 µm and a sintering degree of 0.30 to 0.80 calculated according to the following equation:
sintering degree = (.DELTA.H1 - .DELTA.H3) / (.DELTA.H1 - .DELTA.H2) wherein .DELTA.H1 is heat of fusion of the unsintered polytetrafluoroethylene material, .DELTA.H2 is heat of fusion of the sintered polytetrafluoroethylene material and .DELTA.H3 is heat of fusion of the semisintered polytetrafluoroethylene material.
sintering degree = (.DELTA.H1 - .DELTA.H3) / (.DELTA.H1 - .DELTA.H2) wherein .DELTA.H1 is heat of fusion of the unsintered polytetrafluoroethylene material, .DELTA.H2 is heat of fusion of the sintered polytetrafluoroethylene material and .DELTA.H3 is heat of fusion of the semisintered polytetrafluoroethylene material.
2. The polytetrafluoroethylene porous film according to claim 1, at least one surface of which is laminated with a reinforcing material film selected from the group consisting of olefinic porous material films and fluororesin porous films with or without an adhesive.
3. A polytetrafluoroethylene porous film having an average pore size of from 0.2 to 0.5 µm, an average fibril diameter of from 0.05 to 0.2 µm and a pressure loss of from 10 to 100 mmH2O when air is passed through at a flow rate of 5.3 cm/sec.
4. A polytetrafluoroethylene porous film which is prepared by biaxially stretching a semisintered polytetrafluoroethylene material at an area draw ratio of at least 50 and heat setting the stretched film at a temperature higher than a melting point of sintered polytetrafluoroethylene, said polytetrafluoroethylene porous film having an average fibril diameter of from 0.05 to 0.2 µm and a sintering degree of 0.30 to 0.80 calculated according to the following equation:
sintering degree = (.DELTA.H1 - .DELTA.H3) / (.DELTA.H1 - .DELTA.H2) wherein .DELTA.H2 is heat of fusion of the unsintered polytetrafluoroethylene material, .DELTA.H2 is heat of fusion of the sintered polytetrafluoroethylene material and .DELTA.H3 is heat of fusion of the semisintered polytetrafluoroethylene material.
sintering degree = (.DELTA.H1 - .DELTA.H3) / (.DELTA.H1 - .DELTA.H2) wherein .DELTA.H2 is heat of fusion of the unsintered polytetrafluoroethylene material, .DELTA.H2 is heat of fusion of the sintered polytetrafluoroethylene material and .DELTA.H3 is heat of fusion of the semisintered polytetrafluoroethylene material.
5. The polytetrafluoroethylene porous film according to claim 4, at least one surface of which is laminated with a reinforcing material film selected from the group consisting of olefinic porous material films and fluororesin porous films with or without an adhesive.
6. A process for preparing a polytetrafluoroethylene porous film according to claim 1, comprising the steps of biaxially stretching a semisintered polytetrafluoroethylene at an area draw ratio of at least 50 and heat setting the stretched film at a temperature higher than a melting point of polytetrafluoroethylene.
7. The process according to claim 6, wherein the prepared porous film has a thickness of not larger than about one twentieth of that of the semisintered polytetrafluoroethylene material.
8. An air filter comprising a polytetrafluoroethylene porous film according to claim 1.
9. An air filter comprising a polytetrafluoroethylene porous film according to claim 4.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA002435405A CA2435405A1 (en) | 1991-07-23 | 1992-07-21 | Reinforcing material for a filter material |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18236491 | 1991-07-23 | ||
| JP182364/1991 | 1991-07-23 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002435405A Division CA2435405A1 (en) | 1991-07-23 | 1992-07-21 | Reinforcing material for a filter material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2074349A1 CA2074349A1 (en) | 1993-01-24 |
| CA2074349C true CA2074349C (en) | 2004-04-20 |
Family
ID=16117024
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002074349A Expired - Fee Related CA2074349C (en) | 1991-07-23 | 1992-07-21 | Polytetrafluoroethylene porous film and preparation and use thereof |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US5234739A (en) |
| EP (2) | EP0611790B1 (en) |
| KR (1) | KR100258485B1 (en) |
| CN (1) | CN1033428C (en) |
| CA (1) | CA2074349C (en) |
| DE (2) | DE69208552T2 (en) |
| ES (2) | ES2086591T3 (en) |
| RU (1) | RU2103283C1 (en) |
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| BR112017015987A2 (en) | 2015-02-02 | 2018-03-20 | Du Pont | irrigation system and method for protecting a region of an irrigation pipe |
| US10315141B2 (en) * | 2015-10-29 | 2019-06-11 | Parker Hannifin Filtration (Us), Inc. | Thermally bonded multi-layer felt filtration media |
| JP6861493B2 (en) | 2016-09-30 | 2021-04-21 | 日東電工株式会社 | Air filter filter media, air filter pack and air filter unit |
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| WO2020121981A1 (en) * | 2018-12-10 | 2020-06-18 | ダイキン工業株式会社 | Tetrafluoroethylene polymer, air filter medium, filter pack and air filter unit |
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| CN116512648B (en) * | 2023-07-04 | 2023-12-01 | 江苏源氢新能源科技股份有限公司 | Preparation method of polytetrafluoroethylene high-strength microporous membrane |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CA962021A (en) * | 1970-05-21 | 1975-02-04 | Robert W. Gore | Porous products and process therefor |
| US4049589A (en) * | 1973-03-19 | 1977-09-20 | Sumitomo Electric Industries, Ltd. | Porous films of polytetrafluoroethylene and process for producing said films |
| GB2025835B (en) * | 1978-05-31 | 1982-10-27 | Nitto Electric Ind Co | Producing a porous polytetrafluorethylene article |
| US4596837A (en) * | 1982-02-22 | 1986-06-24 | Daikin Industries Ltd. | Semisintered polytetrafluoroethylene article and production thereof |
| US4671754A (en) * | 1984-03-28 | 1987-06-09 | Sumitomo Electric Industries, Ltd. | Apparatus for manufacturing porous polytetrafluoroethylene material |
| EP0172750A3 (en) * | 1984-08-22 | 1987-03-18 | E.I. Du Pont De Nemours And Company | Porous structures |
| IT1202444B (en) * | 1986-02-21 | 1989-02-09 | Reinmann & Cie Lara | PROCEDURE FOR PRODUCING SHAPED, POROUS BODIES OF ELONGATED SHAPE |
| DE3780511T2 (en) * | 1986-05-23 | 1993-03-04 | Gore & Ass | HIGH PERFORMANCE GAS FILTER. |
| US4743480A (en) * | 1986-11-13 | 1988-05-10 | W. L. Gore & Associates, Inc. | Apparatus and method for extruding and expanding polytetrafluoroethylene tubing and the products produced thereby |
| US4877661A (en) * | 1987-10-19 | 1989-10-31 | W. L. Gore & Associates, Inc. | Rapidly recoverable PTFE and process therefore |
| JP2788976B2 (en) * | 1989-04-26 | 1998-08-20 | ジャパンゴアテック株式会社 | Filter material |
| PL288122A1 (en) * | 1989-12-07 | 1991-08-26 | Daikin Ind Ltd | Method of obtaining a multilayer porous polyterafluoroethylene membrane and partially sintered miltilayer polytetrafluoroethylene product |
-
1992
- 1992-07-21 CA CA002074349A patent/CA2074349C/en not_active Expired - Fee Related
- 1992-07-22 RU SU5052430A patent/RU2103283C1/en not_active IP Right Cessation
- 1992-07-22 US US07/916,618 patent/US5234739A/en not_active Expired - Lifetime
- 1992-07-23 CN CN92108754A patent/CN1033428C/en not_active Expired - Lifetime
- 1992-07-23 EP EP94107246A patent/EP0611790B1/en not_active Expired - Lifetime
- 1992-07-23 EP EP92112569A patent/EP0525630B1/en not_active Expired - Lifetime
- 1992-07-23 DE DE69208552T patent/DE69208552T2/en not_active Expired - Fee Related
- 1992-07-23 DE DE69228002T patent/DE69228002T2/en not_active Expired - Fee Related
- 1992-07-23 ES ES92112569T patent/ES2086591T3/en not_active Expired - Lifetime
- 1992-07-23 KR KR1019920013185A patent/KR100258485B1/en not_active IP Right Cessation
- 1992-07-23 ES ES94107246T patent/ES2126672T3/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| ES2126672T3 (en) | 1999-04-01 |
| KR100258485B1 (en) | 2000-06-15 |
| DE69228002D1 (en) | 1999-02-04 |
| ES2086591T3 (en) | 1996-07-01 |
| US5234739A (en) | 1993-08-10 |
| EP0525630B1 (en) | 1996-02-28 |
| DE69228002T2 (en) | 1999-06-10 |
| DE69208552T2 (en) | 1996-09-05 |
| CN1033428C (en) | 1996-12-04 |
| DE69208552D1 (en) | 1996-04-04 |
| KR930002425A (en) | 1993-02-23 |
| EP0611790A3 (en) | 1994-09-28 |
| RU2103283C1 (en) | 1998-01-27 |
| EP0525630A2 (en) | 1993-02-03 |
| EP0525630A3 (en) | 1993-03-17 |
| CA2074349A1 (en) | 1993-01-24 |
| EP0611790B1 (en) | 1998-12-23 |
| CN1072351A (en) | 1993-05-26 |
| EP0611790A2 (en) | 1994-08-24 |
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