AU4854399A - Extruded thermoplastic foams useful in filtration applications - Google Patents
Extruded thermoplastic foams useful in filtration applications Download PDFInfo
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- AU4854399A AU4854399A AU48543/99A AU4854399A AU4854399A AU 4854399 A AU4854399 A AU 4854399A AU 48543/99 A AU48543/99 A AU 48543/99A AU 4854399 A AU4854399 A AU 4854399A AU 4854399 A AU4854399 A AU 4854399A
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- Australia
- Prior art keywords
- foam
- filter element
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- cell
- percent
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- 239000006260 foam Substances 0.000 title claims description 184
- 238000001914 filtration Methods 0.000 title claims description 34
- 229920001169 thermoplastic Polymers 0.000 title claims description 25
- 239000004416 thermosoftening plastic Substances 0.000 title claims description 25
- 210000004027 cell Anatomy 0.000 claims description 79
- 239000011148 porous material Substances 0.000 claims description 40
- 230000035699 permeability Effects 0.000 claims description 33
- 239000007788 liquid Substances 0.000 claims description 28
- 239000002245 particle Substances 0.000 claims description 28
- 210000002421 cell wall Anatomy 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 22
- 238000001125 extrusion Methods 0.000 claims description 12
- 239000012815 thermoplastic material Substances 0.000 claims description 10
- 150000002148 esters Chemical class 0.000 claims description 3
- 229920000642 polymer Polymers 0.000 description 34
- 239000007789 gas Substances 0.000 description 24
- 239000004604 Blowing Agent Substances 0.000 description 18
- 239000002861 polymer material Substances 0.000 description 16
- 210000003850 cellular structure Anatomy 0.000 description 12
- 238000005187 foaming Methods 0.000 description 11
- 239000004793 Polystyrene Substances 0.000 description 10
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- 229910002092 carbon dioxide Inorganic materials 0.000 description 8
- 229920001577 copolymer Polymers 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 229920002223 polystyrene Polymers 0.000 description 8
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 6
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- 229920001519 homopolymer Polymers 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 4
- 239000005977 Ethylene Substances 0.000 description 4
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 4
- 239000008116 calcium stearate Substances 0.000 description 4
- 235000013539 calcium stearate Nutrition 0.000 description 4
- RWRIWBAIICGTTQ-UHFFFAOYSA-N difluoromethane Chemical compound FCF RWRIWBAIICGTTQ-UHFFFAOYSA-N 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
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- LVGUZGTVOIAKKC-UHFFFAOYSA-N 1,1,1,2-tetrafluoroethane Chemical compound FCC(F)(F)F LVGUZGTVOIAKKC-UHFFFAOYSA-N 0.000 description 3
- NPNPZTNLOVBDOC-UHFFFAOYSA-N 1,1-difluoroethane Chemical compound CC(F)F NPNPZTNLOVBDOC-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 239000004908 Emulsion polymer Substances 0.000 description 3
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000013461 design Methods 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
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- 229920003179 starch-based polymer Polymers 0.000 description 3
- 239000004628 starch-based polymer Substances 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- 239000006269 thermoset foam Substances 0.000 description 3
- UJPMYEOUBPIPHQ-UHFFFAOYSA-N 1,1,1-trifluoroethane Chemical compound CC(F)(F)F UJPMYEOUBPIPHQ-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 230000007812 deficiency Effects 0.000 description 2
- 239000000428 dust Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- BXOUVIIITJXIKB-UHFFFAOYSA-N ethene;styrene Chemical compound C=C.C=CC1=CC=CC=C1 BXOUVIIITJXIKB-UHFFFAOYSA-N 0.000 description 2
- 239000002657 fibrous material Substances 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 230000009477 glass transition Effects 0.000 description 2
- 238000011068 loading method Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000123 paper Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 239000002952 polymeric resin Substances 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 238000001542 size-exclusion chromatography Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 238000011144 upstream manufacturing Methods 0.000 description 2
- 229940051271 1,1-difluoroethane Drugs 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- SBYMUDUGTIKLCR-UHFFFAOYSA-N 2-chloroethenylbenzene Chemical compound ClC=CC1=CC=CC=C1 SBYMUDUGTIKLCR-UHFFFAOYSA-N 0.000 description 1
- WROUWQQRXUBECT-UHFFFAOYSA-N 2-ethylacrylic acid Chemical compound CCC(=C)C(O)=O WROUWQQRXUBECT-UHFFFAOYSA-N 0.000 description 1
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 229920001247 Reticulated foam Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- YMOONIIMQBGTDU-VOTSOKGWSA-N [(e)-2-bromoethenyl]benzene Chemical compound Br\C=C\C1=CC=CC=C1 YMOONIIMQBGTDU-VOTSOKGWSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000002154 agricultural waste Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- MPMBRWOOISTHJV-UHFFFAOYSA-N but-1-enylbenzene Chemical compound CCC=CC1=CC=CC=C1 MPMBRWOOISTHJV-UHFFFAOYSA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000003851 corona treatment Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 230000005686 electrostatic field Effects 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 210000000497 foam cell Anatomy 0.000 description 1
- 239000006261 foam material Substances 0.000 description 1
- 238000013012 foaming technology Methods 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000002440 industrial waste Substances 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000000289 melt material Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000011859 microparticle Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- XQYMIMUDVJCMLU-UHFFFAOYSA-N phenoxyperoxybenzene Chemical compound C=1C=CC=CC=1OOOC1=CC=CC=C1 XQYMIMUDVJCMLU-UHFFFAOYSA-N 0.000 description 1
- 230000036314 physical performance Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000009832 plasma treatment Methods 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001601 polyetherimide Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 229920006327 polystyrene foam Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 229920000131 polyvinylidene Polymers 0.000 description 1
- 238000011045 prefiltration Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 230000000241 respiratory effect Effects 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229920005613 synthetic organic polymer Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D39/00—Filtering material for liquid or gaseous fluids
- B01D39/14—Other self-supporting filtering material ; Other filtering material
- B01D39/16—Other self-supporting filtering material ; Other filtering material of organic material, e.g. synthetic fibres
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D46/00—Filters or filtering processes specially modified for separating dispersed particles from gases or vapours
- B01D46/24—Particle separators, e.g. dust precipitators, using rigid hollow filter bodies
-
- 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
- B01D39/1669—Cellular material
- B01D39/1676—Cellular material of synthetic origin
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Filtering Materials (AREA)
Description
WO 00/06284 PCTIUS99/15020 EXTRUDED THERMOPLASTIC FOAMS USEFUL IN FILTRATION APPLICATIONS The present invention relates to a method of filtration of a gas or liquid by 5 continuously passing either or both of them through extruded, open cell thermoplastic foams which exhibit exceptional permeability. The prior art relates various open cell foams which can be employed in filtration applications. They include both thermoset and thermoplastic foams. Disclosed thermoset foams include those described in U.S. Patent Nos. 3,873,281; 10 4,212,737; 4,303,533; and 4,099,943. Disclosed extruded thermoplastic foams include those described in U.S. Patent Nos. 4,384,032 and 4,427,548 and Great Britain 1,100,727. Disclosed thermoplastic emulsion polymer foams include those described in "Polymeric Foam Materials on Filtration Media," Filtration and Separation, Z. Blumgara, March 1995, pages 245-251. 15 Open cell foams have not been widely employed commercially in filtration applications due to deficiencies in performance compared to other materials, most notably nonwoven fibrous materials. The nature of these performance deficiencies vary according to the structure of the foam. Open cell thermoset foams are used commercially in certain filtration 20 applications but have significant performance limitations. Conventional open cell thermoset foams have reticulated cellular structures (primarily of cell struts without cell walls) and can be manufactured in average cell size ranges above 120 micrometers. A foam with cell struts but without cell walls is illustrated at Handbook of Polymeric Foams and Foam Technology, by Klempner and Frisch, Hanser 25 Publishers @ (1991), page 23, Figure 2a. Commercial foams of this type exhibit relatively high arrestance (70-90 percent) but low efficiency (<20 percent) for particle sizes of 0.3-0.5 micrometers. These foams efficiently filter large particles but do not efficiently filter small particles. These foams are usually recommended for use as air filters for large particles or rocks in lawn or outdoor equipment or as pre 30 filters. There are commercially available microcellular urethane foams made via leaching of soluble salts. Pore sizes are advertised as being as low as 27 microns, but porosity is only up to 80 percent. The limited porosity results in limited permeability and possibly lower life capacity. -1- WO 00/06284 PCT/US99/15020 Open cell emulsion polymer foams have not found significant commercial use in filtration applications. Low density open cell emulsion polymer foams typically have reticulated (primarily cell struts without cell walls) cellular structures and can be manufactured to very small cell sizes of 10 micrometers or less. The 5 open nature of the reticulated cellular structure limits potential filtration efficiency and capacity since small particles can easily pass through it. They are also usually mechanically fragile and subject to flexure and/or compression when a pressure drop is applied across it. Open cell extruded polymer foams have not found significant commercial 10 use in filtration applications. Open cell extruded thermoplastic foams typically have a relatively rigid cellular structure defined substantially by both cell struts and cell walls. Prior art extruded foams disclosed as useful in filtration applications have exhibited higher pressure drops than porous, non-woven fibrous materials of equivalent efficiency due to their relatively low permeability. Prior art foams, even 15 those of relatively high open cell content, that is 90-100 percent open cell, typically have relatively small pores within their cell walls and limited pore incidence level throughout. Thus, they exhibit relatively low permeability. The low permeability translates into high pressure drop for a given foam thickness. It would be desirable to have an extruded, open-cell thermoplastic foam 20 which has a relatively rigid cellular structure defined substantially by both cell walls and cell struts and which exhibits relatively high permeability for liquids and gases. It would also be desirable to have a foam which exhibits low pressure drop for a given desired efficiency, capacity, and/or foam thickness. It would also be desirable to have a foam which exhibits improved efficiency in filtering small particles of 0.3-0.5 25 micrometers. This invention provides a filter element made to fit within a filter element housing, the filter element comprising an extruded open-cell thermoplastic foam having a structure substantially of cell walls and cell struts, an overall open-cell content of 50 percent or more, an average cell size of 1.5 millimeters or less, and a 30 permeability coefficient of 6x10' 3 m 2 or more, and, optionally, retaining means for the foam. This invention provides a method of filtration comprising passing a liquid or gas through a filter element made to fit within a filter element housing, the filter element comprising an extruded open-cell thermoplastic foam having a structure -2- WO 00/06284 PCT/US99/15020 substantially of cell walls and cell struts, an overall open-cell content of 50 percent or more, an average cell size of 1.5 millimeters or less, and a permeability of 6x10 13 m2 or more, and, optionally, retaining means for the foam. Also provided by this invention is a method of filtration comprising passing a 5 liquid or gas through an extruded, open-cell thermoplastic foam having a structure substantially of cell walls and cell struts, an overall open-cell content of 50 percent or more, an average cell size of 1.5 millimeters or less, and a permeability of 6x1 0~ m 2 or more. Figure 1 shows a foam filter useful in the present invention. The filter has a 10 cylindrical shape. Figure 2 shows another embodiment of a foam filter useful in the present invention. The filter is in the form of a pleated foam sheet. Figure 3 shows another embodiment of a foam filter for liquids or gases useful in the present invention. The filter is partially perforated. 15 This invention provides a filter element made to fit within a filter element housing. Filter element housings are well known in the art in various applications involving the filtration of fluids such as gases and liquids. The filter element of this invention may be substially the foam itself, or the filter element may employ retaining means to hold the foam. The retaining means may be any material know 20 in the art including plastics, metals, wood, paper, etc. The filter element and the method of filtration of the present invention employ certain extruded, open-cell thermoplastic foams which exhibit outstanding filtration performance for both liquids and gases. The foams exhibit a greater permeability than would be expected for foams having a substantially cell strut/cell 25 wall structure. The enhanced permeability enables such foams to be efficacious in conventional commercial, residential, and industrial filtration applications. The extruded open cell foams exhibit permeability coefficients for air of 6 x 101 m2 or more, or 1.44 x 10- m2 or more, desirably 3 x 101 m2 or more, more desirably 4.28 x 10 m2 or more, and preferably 8 x 10 m2 or more, more 30 preferalby 1.6 x 10- m2 or more, and still more preferalblyl.6 x 10- m2 or more. Permeability is determined according to the following formula: Ke =QL AP -3- WO 00/06284 PCT/US99/15020 where A = area (square meters (M 2 )) Q = volumetric flow rate of air (cubic meters/second (m 3 /sec)) P = differential pressure (Pascals (Pa)) L = thickness of the foam (meters (m)) = kinematic viscosity of air (Newton -seconds/square meter (Ns/ M 2 )) Ke = permeability coefficient (square meters (M 2 )) The formula is described in Handbook of Filter Media by Derek B. Purchas, 1s' Edition, Elsevier Science Ltd. @ 1996, pages 488-89. In the description herein involving numerical values for permeability, it should be understood that 5 occasionally the trerms "permeability" and "permeability coefficient" are used interchangeably. Although not bound by any particular theory, extruded foams useful in the present invention are believed to derive their enhanced permeability from their unique foam structure. The foams have an open cellular structure having 10 substantially both cell walls and cell struts wherein the cellular structure defines any or a combination of the following: enhanced (greater) incidence of pores within cell walls, enhanced (larger) pores sizes within the cell walls, enhanced (greater) proportion of cell walls generally vertical and horizontal to the extrusion direction having pores therein, and a minor proportion of cell walls missing or substantially 15 missing. Prior art extruded filtration foams lack these structural features to the extent required to achieve the permeabilities disclosed herein for the foams employed in the present method. The enhanced permeability affords improved design flexibility with respect to efficiency, capacity, pressure drop, and foam thickness. 20 Extruded foams useful in the present invention afford improved performance advantages over reticulated prior art foams. The substantially cell wall/cell strut cellular structure of the foam of the present method provides a relatively tortuous pore pathway for the liquid or gas to traverse and provides substantial pockets, crevices, and surface area into which particles can lodge themselves. The cellular 25 structure affords improved design flexibility with respect to efficiency, capacity, pressure drop, and foam thickness compared to reticulated foams. The foam has an open cell content of 50 percent or more, preferably 70 percent or more, more preferably 90 percent or more, and most preferably 95 -4- WO 00/06284 PCT/US99/15020 percent or more according to ASTM D2856-A. Permeability can increase as open cell content increases. The present invention is efficacious at a wide range of foam cell sizes. The foam desirably has an average cell size of 1.5 millimeters or less, more desirably, 5 an average cell size of 1 millimeter or less, preferably, an average cell size of 0.1 millimeter or less, and more preferably 0.01 to 1.0 millimeters (10 to 1000 micrometers) according to ASTM D3576-77. One useful foam embodiment has an average cell size of 0.2 to 0.7 millimeters (200 to 700 micrometers) according to ASTM D3576-77. Another useful foam embodiment has an average cell size of 10 0.01 to 0.07 millimeters (10 to 70 micrometers) according to ASTM D3576-77. The foam can have a mean flow pore diameter (m.f.p.d.) of from 0.1 to 50 micrometers. Desired levels of m.f.p.d. will vary depending on the sizes of microparticles to be filtered, the medium to be filtered (liquid or gas or both), desired efficiency levels, and desired pressure drop levels. Useful m.p.f.d. ranges include 15 0.1 micrometers or more, 1 micrometer or more, 5 micrometers or more, 10 micrometers or more, and 15 micrometers or more. Average cell size and m.p.f.d differ in that average cell size relates to average cell dimension in the foam and m.p.f.d relates to the mean pore size at which one half of total air flow occurs through pores greater in size than the mean pore size and half through pores less in 20 size than the mean pore size. The m.f.p.d. may be determined using an automated porometer, such as the Perm Porometer 200 PSI by PMI (Porous Materials, Inc.), with a perfluoro compound C5-18 fluid such as Fluoroinert FC-40 (Sigma Chemical Corp.). Preferred ranges for alternative embodiments include m.f.p.d. ranges of from 25 3 to 8 micrometers, from 8 to 20 micrometers and from 20 to 50 micrometers. Foams which exhibit a wide range of efficiencies are possible in the present invention. A particular efficiency level or range may depend upon the desired commercial application. Typically, efficiencies will range from 40 to substantially 100 percent and any point in between for air streams. Efficiency can be determined 30 by one of two methods single-pass challenge tests. In ASTM 2986-71 a monodisperse aerosol of 0.3 micron DOP particles is generated via an aerosol generator. The aerosol is drawn through the specimen at 10 fpm (5 m/sec). The penetration is measured through the aid of a particle counter on each side of the filter. -5- WO 00/06284 PCT/US99/15020 The penetration P is defined as: P = (Particle conc. downstream / Particle Conc. upstream) Efficiency, E, defined as one minus the penetration, or E = 1 - P A second method involves the generation of a polydisperse aerosol 5 concentration and measuring the particle concentration via a size-discriminating detector. Penetration and efficiency are measured in the same manner described above. The test method used for the data in this case utilized a polydisperse aerosol of NaCl and KCl solutions. The particles were generated via an AT300 generator 10 from TSI Incorporated. An HIAC/Royco 5109 particle counter was used to determine the efficiency. Efficiencies were measured over a range of face velocities. The face velocity is the volumetric flow rate divided by the cross-sectional are of the filter media. Values reported are performed at a phase velocity of 10 feet per minute. 15 Desirable efficienies for the foams for use in this invention include 40 percent or more for particle sizes of 0.3 micrometers, 90 percent or more for particle sizes of 0.3 micrometers, 99 percent or more for particle sizes of 0.3 micrometers. A preferred efficieny for high efficiency filters is 99.991 percent or more for particle sizes of 0.3 micrometers. A preferred range of efficiencies for one embodiment is 20 from 40 to 70 percent or more for particle sizes of from 0.3 to 0.5 micrometers. The foam has a density of preferably from 16 to 250 kilograms per cubic meter (kg/m 3 ) and more preferably from 25 to 100 kg/m 3 according to ASTM D 1622-88. One useful embodiment of the invention employs an extruded foam having a 25 structure substantially of cell walls and cell struts, an overall open-cell content of 50 percent or more (preferably 90 percent or more), and an average cell size of 0.1 millimeters (100 micrometers) or less. Foams of such cell sizes are useful because they permit gases and liquids to be filtered for particles of sizes too small for known extruded foam filters. Foaming with small cell sizes induces formation of thinner 30 cell walls, which can have pores more easily formed therein with respect to both incidence level and pore size. Use of such a foam as a filter is heretofore unknown in the art. Another useful embodiment the invention employs an extruded foam have a structure substantially of cell walls and cell struts, an overall open-cell content of 50 -6- WO 00/06284 PCT/US99/15020 percent or more, an average cell size of 0.1 millimeters (100 micrometers) or more, and a mean flow pore diameter of 10 micrometers or more. Foams of such cell sizes are useful because they permit gases and liquids to be filtered for particles of size 0.3 to 0.5 micrometers at moderate efficiency levels for air (40 to 70 percent) 5 with a permeability coefficient of 1.6 x 10-11 m 2 or more for air. Use of such a foam is heretofore unknown in the filtration art. Additional foam embodiments useful in the present method are set forth below in Table 1. As is apparent, the foams may have ranges of desirable physical property and performance parameters. The foams of #1 generally correspond in 10 performance to those of HEPA non-woven fiber filters. The foams of #2 generally correspond in performance to those of non-woven fiber filters typically used in applications requiring 98 percent ASHRAE filters. The foams of #3 generally correspond in performance to those of non-woven fiber filters typically used in applications requiring 60-70 percent ASHRAE filters. -7- WO 00/06284 PCTIUS99/15020 Table 1 Additional Foam Embodiments Foam M.F.P.D. Cell Size Permeability Efficiency (micrometers) (micrometers) (M 2 ) (Percent) #1 100 3-8 >1.44x10-" 99.991 #2 100 8-20 >4.28x10 90 #3 100 20-50 >4.18x10 11 40 5 -M.F.P.D. = Mean Flow Pore Diameter 2 -m = meters squared -efficiency is determined according to ASTM D2986-71 for air at 10 feet/minutes (0.05 meters/second) phase velocity 10 Photomicrographs of the cellular structure of foams useful in the present invention include those shown in Figures 1-5 of U.S. Serial No. 09/096,029, filed June 11, 1998. The foam may take any physical configuration known in the art such as sheet, plank, pleat, tube, rod, or cylinder. Desirable sheet foams include those less than 0.375 inch in thickness in cross-section. Desirable plank foams include 15 those having in cross-section thickness of 0.375 inch (0.95 cm) or more. Useful sheet foams can be made by skiving or slicing extruded plank foams by knife or hot (heated) wire into two or more plies or sheets. Desirably, the skin layers of the foam are sliced, skived, or planed off or otherwise removed to better expose the open cell structure of the foam. 20 The present method is useful in a variety of conventional residential, industrial, and agricultural liquid/gas filter applications. Liquid filter applications include water filters, industrial and agricultural waste/effluent and/or recycle filters, chemical filters, oil filters, and backflushing filters. Suitable gas filtration applications include air intakes in furnaces and air conditioners, industrial air circulation and 25 blower systems, residential air cleaners, dust collection and removal systems, fume and vapor emission control systems, compressed air systems, and respiratory masks. A useful industrial application is a sheet foam formed into a flexible bag for WO 00/06284 PCT/US99/15020 use as a bag house filter. The foam is also useful as a pre-filter upstream of other filter materials. Figure 1 shows a cylindrical filter 10 for gases or liquids. Cylinder 10 defines a channel 12 extending from one end of filter 10 to the other. As shown, a liquid or 5 gas to be filtered may enter cylinder 10 under pressure through an orifice 14. A liquid or gas may also enter cylinder 10 under pressure through orifice 16, or, alternately, orifice 16 may be blocked off in favor of orifice 14. Upon entering channel 12, the liquid or gas is forced radially through a cylindrical-shaped foam media 18 to effect filtration. Cylindrical filters such as the one shown in Figure 1 are 10 typically employed commercially in cylindrical cartridges for residential, industrial, and agricultural applications. One embodiment of such a cylindrical filter has an outside diameter (foam media diameter) of approximately 3 inches (7.62 centimeters) and an inside diameter (channel diameter) of approximately 1 inch (2.54 centimeters). 15 Figure 2 shows a pleated filter 20 having a sheet foam media 22 which is folded continuously along its length to form pleats 24 therein. Gas or liquid is forced through filter 20 under pressure to effect filtration. Another embodiment of a pleated filter is a filter having pleats within pleats (not shown). In other words, the filter would have relatively larger primary pleats and relatively smaller secondary 20 pleats within the primary pleats. Use of a pleated configuration allows the gas or liquid to be exposed to a greater surface and volume of foam media. Pleated filters are commonly employed in home and industrial furnace air intakes. Figure 3 shows a filter 30 having a foam media 32 which has a plurality or multiplicity of perforations 34 extending partially through it from a face or surface 36 25 opposite to the gas or liquid stream. The presence of such perforations is to enable pressure drop across the foam media to be reduced yet provide much of the advantage of the efficiency and capacity afforded by a thicker foam. Alternately, a foam (not shown) may have perforations extending partially through it from a face or surface which is directional to the gas or liquid stream. In that instance, the 30 perforations effectively increase the surface area to which the gas or liquid stream is exposed, which can increase filtration efficiency and capacity. Filtration may take place through the extruded foam in the extrusion direction or transverse (vertical or horizontal) direction or in a combination of the three directions. -9- WO 00/06284 PCT/US99/15020 If desired, the foam can be manufactured and/or fabricated to have a gradient through it wherein the m.f.p.d. of the cellular structure of the foam changes from one surface of the filter to the opposing surface. For instance, the foam can have a gradient wherein the m.f.p.d. changes from relatively high to relatively low or 5 vice versa. The liquid or gas can be passed from the region of high m.f.p.d. to the region of low m.f.p.d. or vice versa depending upon the desired function and performance of the filter. Typically, liquid or gas will be passed from a region of high m.f.p.d. to a region of low m.f.p.d. so that larger particles will be filtered out first and be less likely to clog small pores; smaller particles are then subsequently 10 filtered in the region of low m.f.p.d. A preferred method of making a foam having a m.f.p.d. gradient through it is to extrude a plank foam of 10 millimeters thickness or more in cross-section. Thick extruded foams will typically exhibit a cellular structure which varies in physical properties such as density, cell size, and pore size depending upon position in the 15 cross-section. Density typically increases from the middle region to a skin region. Cell size and pore size typically decrease from the middle region to a skin region. An extruded foam can be cut or sliced at a given region of the foam to yield a foam portion of a desired gradient cellular structure. If desired, filtration efficiency and capacity can be enhanced by rendering 20 the foams electrostatic by any means know in the art. Electrostatic agents can be incorporated into the polymer resin during manufacture of the foam or be deposited on the internal surfaces of the foam. The intemal surfaces of the foam may also be exposed to corona discharge or plasma treatment. The foam may also be exposed to an electrostatic field when filtration is occurring. Regardless of the method of 25 treatment, the entire foam may be treated or merely one or more surfaces or regions thereof. Extruded thermoplastic foams are generally prepared by heating a thermoplastic material to form a plasticized or melt polymer material, incorporating therein a blowing agent to form a foamable gel, and extruding the gel through a die 30 to form the foam product. Prior to mixing with the blowing agent, the polymer material is heated to a temperature at or above its glass transition temperature or melting point. The blowing agent may be incorporated or mixed into the melt polymer material by any means known in the art such as with an extruder, mixer, blender, or the like. The blowing agent is mixed with the melt polymer material at an -10- WO 00/06284 PCT/US99/15020 elevated pressure sufficient to prevent substantial expansion of the melt polymer material and to generally disperse the blowing agent homogeneously therein. Optionally nucleating agent may be blended in the polymer melt or dry blended with the polymer material prior to plasticizing or melting. The foamable gel is typically 5 cooled to a lower temperature to optimize or attain desired physical characteristics of the foam. The gel may be cooled in the extruder or other mixing device or in separate coolers. The gel is then extruded or conveyed through a die of desired shape to a zone of reduced or lower pressure to form the foam. The zone of lower pressure is at a pressure lower than that in which the foamable gel is maintained 10 prior to extrusion through the die. The lower pressure may be superatmospheric or subatmospheric (vacuum), but is preferably at an atmospheric level. As the extrudate exits and expands from the die, the foam is optionally elongated by mechanical means to assist in pore formation and open cell formation. Elongation is discussed below. 15 To assist in extruding open-cell thermoplastic foams, it may be advantageous to employ a polymer different than the predominant polymer employed in the thermoplastic material. Employing a minor amount of a polymer different than the predominate polymer enhances open cell content development. For example, in making a polystyrene foam, minor amounts of polyethylene or 20 ethylene/vinyl acetate copolymer may be employed. In making a polyethylene foam, minor amounts of polystyrene may be employed. Useful teachings to preferred different polymers are seen in U.S. Serial No. 08/880,954.Extruded open cell thermoplastic foams may be made according to the general extrusion teachings herein and optionally may be exposed to the additional processing step of 25 elongating the extrudate as it exits and expands from the extrusion die to form the foam. Elongation can increase the relative proportion of cell walls having pores therein and/or increase the average size of existing pores. Extensive teachings to elongation are seen in U.S. Serial No. 60/049181, filed June 11, 1997, and U. S. Serial No. 09/096,029, filed June 11, 1998. 30 The foam may be formed of any thermoplastic which can be formed or blown into an open cell foam of sufficient permeability. Useful thermoplastics may include natural and synthetic organic polymers. Suitable plastics may include polyolefins, polyvinylchloride, alkenyl aromatic polymers, cellulosic polymers, polycarbonates, starch-based polymers, polyetherimides, polyamides, polyesters, polyvinylidene -11- WO 00/06284 PCT/US99/15020 chlorides, polymethylmethacrylates, copolymer/polymer blends, and rubber modified polymers. Suitable alkenyl aromatic polymers include polystyrene and copolymers of styrene and other copolymerizable monomers. Some very desirable embodiments are those in which the thermoplastic 5 material compromises in polymerized form 50 percent or more by weight alkenyl aromatic monomeric units, or the thermoplastic material compromises in polymerized form 50 percent or more by weight ethylenic monomeric units, or the thermoplastic material compromises in polymerized form 50 percent or more by weight propyleneic monomeric units, or the thermoplastic material compromises in 10 polymerized form 50 percent or more by weight ester monomeric units. If desired, the foam can be blown from a thermoplastic material which is partially or substantially biodegradable. Useful polymers include cellulosic polymers, starch-based polymers, and blends of starch-based polymers and phenoxy ether polymers. 15 A particularly useful thermoplastic foam comprises an alkenyl aromatic polymer material. Suitable alkenyl aromatic polymer materials include alkenyl aromatic homopolymers and copolymers of alkenyl aromatic compounds and copolymerizable ethylenically unsaturated comonomers. The alkenyl aromatic polymer material may further include minor proportions of non-alkenyl aromatic 20 polymers. The alkenyl aromatic polymer material may be comprised solely of one or more alkenyl aromatic homopolymers, one or more alkenyl aromatic copolymers, a blend of one or more of each of alkenyl aromatic homopolymers and copolymers, or blends of any of the foregoing with a non-alkenyl aromatic polymer. Regardless of composition, the alkenyl aromatic polymer material comprises greater than 50 and 25 preferably greater than 70 weight percent alkenyl aromatic monomeric units. Most preferably, the alkenyl aromatic polymer material is comprised entirely of alkenyl aromatic monomeric units. Suitable alkenyl aromatic polymers include those derived from alkenyl aromatic compounds such as styrene, alphamethylstyrene, ethylstyrene, vinyl 30 benzene, vinyl toluene, chlorostyrene, and bromostyrene. A preferred alkenyl aromatic polymer is polystyrene. Minor amounts of monoethylenically unsaturated compounds such as C2-6 alkyl acids and esters, ionomeric derivatives, and C4-6 dienes may be copolymerized with alkenyl aromatic compounds. Examples of copolymerizable compounds include acrylic acid, methacrylic acid, ethacrylic acid, -12- WO 00/06284 PCT/US99/15020 maleic acid, itaconic acid, acrylonitrile, maleic anhydride, methyl acrylate, ethyl acrylate, isobutyl acrylate, n-butyl acrylate, methyl methacrylate, vinyl acetate and butadiene. Useful foams can comprise substantially (that is greater than 95 percent by weight) and most preferably entirely of polystyrene. Useful foams can comprise 5 polystyrene of 125,000 to 300,000 weight average molecular weight, 135,000 to 200,000 weight average molecular weight, 165,000 to 200,000 weight average molecular weight, and 135,000 to 165,000 weight average molecular weight according to size exclusion chromatography. Useful extruded thermoplastic foams include extruded microcellular alkenyl 10 aromatic polymer foams of high open cell content and processes for making as disclosed in WO 96/34038. The disclosed foams have an average cell size of 70 micrometers or less and an open cell content of 70 percent or more. In the process disclosed in WO 96/34038, useful blowing agents include 1 ,1 difluoroethane (HFC-152a), 1,1,1-trifluoroethane (HFC-143a), 1,1,1,2 15 tetrafluoroethane (HFC-134a), chlorodifluoromethane (HCFC-22), carbon dioxide (C02), and difluoromethane (HFC-32). Preferred blowing agents are HFC-152a, HFC-134a, and carbon dioxide. The above blowing agents will comprise 50 mole percent or more and preferably 70 percent or more of the total number of moles of blowing agent. The balance may be made up of other blowing agents. The amount 20 of blowing agent employed is from 0.06 to 0.17 gram-moles per 100 grams of polymer, preferably from 0.08 to 0.14 gram-moles per 100 grams of polymer, and most preferably from 0.08-0.12 gram-moles per 100 grams of polymer. The use of a relatively small amount of blowing agent allows formation of a foam with a high open cell content. Preferred foaming temperatures will vary from 1180C to 160*C. 25 Most preferred foaming temperatures will vary from 1180C to 1300C, especially for larger size foam production lines. Smaller lines will run hotter. The amount of nucleating agent employed may range from 0.01 to 5 parts by weight per hundred parts by weight of a polymer resin. The preferred range is from 0.1 to 3 parts by weight. 30 Another extruded alkenyl aromatic foam of larger average cell size and processes for making are seen in WO 96/00258. Open-cell content is 30 percent or more according to ASTM D2856-87. The disclosed foams have a density of 1.5 pcf to 6.0 pcf (24 kg/m 3 to 96 kg/m 3 ) and preferably a density of 1.8 pcf to 3.5 pcf (32 -13- WO 00/06284 PCT/US99/15020 kg/m 3 to 48 kg/m 3 ) according to ASTM D-1 622-88. The present foam has an average cell size of from 0.08 millimeters (mm) to 1.2 mm and preferably from 0.10 mm to 0.9 mm according to ASTM D3576-77. In the process for making the foam in WO 96/00258, the foaming 5 temperature, which is relatively higher than that for making closed-cell foams (less than 10 percent open-cell according to ASTM D2856-87), may vary from 11 8'C to 1450C. Foaming temperature will vary according to nucleating agent composition and concentration, blowing agent composition and concentration, polymer material characteristics, and extrusion die design. The foaming temperature for the present 10 open-cell foam varies from 30C to 150C and preferably 10*C to 150C higher than the highest foaming temperature for a corresponding closed-cell foam (less than 10 percent open-cell according to ASTM D2856-87) of substantially equivalent density and cell size made with a substantially equivalent composition (including polymer material, nucleating agent, additives, and blowing agent) in a substantially 15 equivalent process. A preferred foaming temperature is at 330C or more higher than the glass transition temperature (according to ASTM D-3418) of the alkenyl aromatic polymer material. A most preferred foaming temperature is from 1350C to 1400C. The amount of blowing agent incorporated into the polymer melt material to make a foam-forming gel is from 0.2 to 5.0 gram-moles per kilogram of polymer, 20 preferably from 0.5 to 3.0 gram-moles per kilogram of polymer, and most preferably from 0.7 to 2.0 gram-moles per kilogram of polymer. A nucleating agent such as those described above may be employed. To make foams of the physical properties described in WO 96/00258 which have the pore size and pore incidence level to be effective in the present invention, it may be necessary to incorporate 25 different polymers into the alkenyl aromatic polymer material such as polyolefins of melting temperatures of 700C or less, ethylene/styrene interpolymers, and styrene/butadiene copolymers or other rubbery homopolymers or copolymers. Useful extruded, open cell thermoplastic foams include those made of styrene/ethylene interpolymers and blends of such interpolymers with alkenyl 30 aromatic polymers and ethylene polymers described in U.S. Patent No. 5,460,818, WO 96/14233, and U.S. Serial No. 60/078091, filed March 16, 1998. Such interpolymers are particularly useful in making foams having an average cell size of greater than 100 micrometers. -14- WO 00/06284 PCT/US99/15020 In making extruded foams, other additives may be incorporated such as inorganic fillers, pigments, antioxidants, acid scavengers, ultraviolet absorbers, flame retardants, processing aids, and extrusion aids. The following are examples of the present invention, and are not to be 5 construed as limiting. Unless otherwise indicated, all percentages, parts, or proportions are by weight. EXAMPLES Various extruded thermoplastic foams useful in the present invention were prepared and tested for filtration capability. 10 The foams were prepared in two apparatuses each comprising an extruder, a mixer, a cooler, and an extrusion die in series. Polymer and additives were melted and mixed in the extruder and conveyed to the mixer in the form of a polymer melt. Blowing agent was incorporated in the melt in the mixer to form a polymer gel. The gel was conveyed through the cooler to cool it to a desirable 15 foaming temperature. The gel was then conveyed through an orifice in the extrusion die into atmospheric pressure to expand to form the foam. Forming plates were positioned at the exit of the die to restrict expansion in the vertical direction and facilitate expansion in the horizontal and extrusion directions. A polystyrene resin of 135,000 weight average molecular weight according 20 to size exclusion chromatography was employed. The other polymer employed was an ethylene/styrene interpolymer (ESI) of 69 percent styrene monomeric content by weight, less than 5 percent styrene homopolymer (polystyrene), and the remainder ethylene monomeric content by weight. Additives included talc as a nucleating agent, ethylene/vinyl acetate copolymer (EVA) to aid in open cell formation, and 25 calcium stearate (CaSt) as an extruder lubricant. Polymers, additives, and blowing agents employed as well as certain process conditions are set forth in Table 2. Foam and filtration properties are set forth in Table 3. The density of the foam was measured according to ASTM D 1622-88. ASTM D2856-A was used to determine the open cell content of the foam 30 and cell size was determined according to ASTMD3576-77. The mean flow pore diameter (m.f.p.d.) was determined by using an Automated Perm Porometer 200 PSI from Porous Materials, Inc. (PMI) with Fluoroinert FC-40 compound. The test procedure and equipment are discussed in PMI literature as well as papers presented at INDA-TEC 1996 and FILTRATION 97 (page 12.0). In this test, the -15- WO 00/06284 PCT/US99/15020 mean flow pore diameter is interpreted as the pore size at which half of the total air flow through a sample occurs through pores larger than the mean and half of the air flow occurs through pores smaller than the mean. The test procedure and equipment used to determine the efficiency and 5 pressure drop across the foam filter are described in Filtration and Separation, March 1998 pages 118-122. The open cell foams used as filters in this test were 24" by 24 "and ranged in thickness from1.52 to 0.16" in thickness. Sampling time for the tests was 60 seconds. A polydisperse aerosol of KCI was used as the test dust. Efficiencies and pressure drops were measured at media face velocities of 10 10, 20 30 and 40 feet per minute. -16- WO 00/06284 PCT/US99/15020 Table 2 Example # Polymer Additives Blowing Agent Foaming and loadings and Loading Temperature (OC) 1 Polystyrene EVA 1.0pph 5.6 pph 134a 130 CaSt 0.5pph 2.4 pph C02 2 Polystyrene EVA 1.0pph 2.8 pph 134a CaSt 0.5pph 2.4 pph C02 119 1.8 pph EtCl 3 PS / ESI Talc 4.2 pph CO2 119 (20% ESI) 1.1 pph 134a 4 PS / ESI Talc 3.7 pph EtCl 130 (10%ESI) 2.4 pph C02 5 PS / EG81 00 3.7 pph EtCl (10% EG81 00) 2.4 pph C02 140 -17 SUBSTITUTE SHEET (RULE 26) WO 00/06284 PCTIUS99/1 5020 7 7 7 - 7 - -Ec C) CD 0 C 0) E ;- - r - - - "; ' (-0 (0 C) tO j No m C) __ c U) 0 - 0- -~ cc cc cc -0 Q 0 -~0 C)~6 6 C 0 Q) 00 Eo (DN\ - N' c'j co) u- E m M ') CD0 E toE cc ' ~0) tO 0)Xn. (D0_ r 0 - C CD0 )0 CD- 0) CO) H~ 0 LL0L z 0) CV ( a 0~~~ ~ ~ C: ) : (D~~~~~~c (Z C. - - - - CJCJCJ0 a .0~~~ LL(Dc~ M > LU Em _ C) oE 0 -= C-) o 0) 0 S0 0 0)~~~~~ C) C t o C) CC 0) ) C C) C) C) ) C - 0 C C:0 ) " c~ 0*- 0- - 0 0 ~0 0 cz ~~~Ec (n 0m (n c ~ cu 00 n C' CNJ 0 to m6 Nr iN Q0 0) -D cc to Ec -t 0 m - c z LU E -18- WO 00/06284 PCT/US99/15020 While embodiments of the foam and the methods of the present invention have been shown with regard to specific details, it will be appreciated that depending upon the manufacturing process and the manufacturer's desires, the present invention may be 5 modified by various changes while still being fairly within the scope of the novel teachings and principles herein set forth. 19
Claims (38)
1. A filter element made to fit within a filter element housing, the filter element comprising an extruded open-cell thermoplastic foam having a structure substantially of cell walls and cell struts, an overall open-cell content of about 50 percent or more, an average 5 cell size of about 1.5 millimeters or less, and a permeability coefficient of about 6x10~3 m2 or more, and, optionally, retaining means for the foam.
2. The filter element of Claim 1, wherein the foam has a permeability coefficient of about 1.44x1 02 m2 or more.
3. The filter element of Claim 2, wherein the foam has a permeability coefficient 10 of about 3x10~2 m2 or more.
4. The filter element of Claim 3, wherein the foam has a permeability coefficient of about 4.28x1 0-2 m2 or more.
5. The filter element of Claim 4, wherein the foam has a permeability coefficient of about 8x10 ~ m2 or more. 15
6. The filter element of Claim 5, wherein the foam has a permeability coefficient of about 1.6x10-11 m 2 or more.
7. The filter element of Claim 6, wherein the foam has a permeability coefficient of about 4.18x10" m2 or more.
8. The filter element of one of Claims 1-7, wherein the foam has a mean flow 20 pore diameter of about 0.1 micrometers to about 50 micrometers.
9. The filter element of one of Claims 1-7, wherein the foam has a mean flow pore diameter of about 1 micrometers or more.
10. The filter element of Claim 9, wherein the foam has an mean flow pore diameter of about 5 micrometers or more. 25
11. The filter element of Claim 10, wherein the foam has a mean flow pore diameter of about 10 micrometers or more.
12. The filter element of Claim 11, the foam having a mean flow pore diameter of about 15 micrometers or more.
13. The filter element of one of Claims 1-7, the foam having a mean flow pore 30 diameter of from about 3 to about 8 micrometers.
14. The filter element of one of Claims 1-7, the foam having a mean flow pore diameter of from about 8 to about 20 micrometers.
15. The filter element of one of Claims 1-7, the foam having a mean flow pore diameter of from about 20 to about 50 micrometers. 20 WO 00/06284 PCT/US99/15020
16. The filter element of one of Claims 1-15, wherein the thermoplastic material compromises in polymerized form 50 percent or more by weight alkenyl aromatic monomeric units.
17. The filter element of one of Claims 1-15, wherein the thermoplastic material 5 compromises in polymerized form 50 percent or more by weight ethylenic monomeric units.
18. The filter element of one of Claims 1-15, wherein the thermoplastic material compromises in polymerized form 50 percent or more by weight propyleneic monomeric units.
19. The filter element of one of Claims 1-15, wherein the thermoplastic material 10 compromises in polymerized form 50 percent or more by weight ester monomeric units.
20. The filter element of one of Claims 1-19, wherein the open-cell content is 70 percent or more.
21. The filter element of Claim 20, wherein the open-cell content is 90 percent or more. 15
22. The filter element of Claim 21, wherein the open-cell content is 95 percent or more.
23. The filter element of one of Claims 1-22, wherein the foam has an average cell size of 1 millimeter or less.
24. The filter element of Claim 23, wherein the foam has an average cell size of 20 0.1 millimeter or less.
25. The filter element of one of Claims 1-22, wherein the foam has an average cell size of from 0.01 to 1.0 millimeter.
26. The filter element of Claim 25, wherein the foam has an average cell size of from 10 to 70 micrometers, or wherein the foam has an average cell size of from 200 to 700 25 micrometers.
27. The filter element of one of Claims 1-22, wherein the foam has an average cell size of 100 micrometers or more.
28. The filter element of one of Claims 1-27, wherein the foam has an efficiency of 40 percent or more for particle sizes of 0.3 micrometers. 30
29. The filter element of Claim 28, wherein the foam has an efficiency of 90 percent or more for particle sizes of 0.3 micrometers.
30. The filter element of Claim 29, wherein the foam has an efficiency of 99 percent or more for particle sizes of 0.3 micrometers.
31. The filter element of Claim 30, wherein the foam has an efficiency of 99.991 35 percent or more for particle sizes of 0.3 micrometers. 21 WO 00/06284 PCT/US99/15020
32. The filter element of one of Claims 1-27, wherein the foam has an efficiency of from 40 to 70 percent or more for particle sizes of from 0.3 to 0.5 micrometers.
33. The filter element of one of Claims 1-32, wherein the density of the foam is from 16 to 250 kg/cubic meter. 5
34. The filter element of Claim 33, wherein the density of the foam is from 25 to 100 kg/cubic meter.
35. A method of filtration comprising passing a liquid or gas through an extruded, open-cell thermoplastic foam having a structure substantially of cell walls and cell struts, an overall open-cell content of 50 percent or more, an average cell size of 1.5 millimeters or 10 less, and a permeability of 6x1 01 m2 or more.
36. A method of filtration comprising passing a liquid or gas through a filter element made to fit within a filter element housing, the filter element comprising an extruded open-cell thermoplastic foam having a structure substantially of cell walls and cell struts, an overall open-cell content of 50 percent or more, an average cell size of 1.5 millimeters or 15 less, and a permeability of 6x10~" m2 or more, and, optionally, retaining means for the foam.
37. The method of one of Claims 35-36, wherein the liquid or gas is passed through the foam substantially in the extrusion direction.
38. The method of one of Claims 35-36, wherein the liquid or gas is passed 20 through the foam substantially transverse to the extrusion direction. 22
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US60094504 | 1998-07-29 | ||
PCT/US1999/015020 WO2000006284A1 (en) | 1998-07-29 | 1999-07-02 | Extruded thermoplastic foams useful in filtration applications |
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AU4854399A true AU4854399A (en) | 2000-02-21 |
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AU48543/99A Abandoned AU4854399A (en) | 1998-07-29 | 1999-07-02 | Extruded thermoplastic foams useful in filtration applications |
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JP (1) | JP2002521188A (en) |
KR (1) | KR20010072094A (en) |
CN (1) | CN1306452A (en) |
AR (1) | AR019945A1 (en) |
AU (1) | AU4854399A (en) |
BR (1) | BR9912425A (en) |
CA (1) | CA2332815A1 (en) |
TW (1) | TW469156B (en) |
WO (1) | WO2000006284A1 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102005054273A1 (en) * | 2005-11-11 | 2007-05-16 | Freudenberg Carl Kg | Filter element for removing different sized particles from flowing fluid, contains porous filter material(s) with locally increasing or decreasing pore size |
CA3034840A1 (en) * | 2016-08-26 | 2018-03-01 | 3M Innovative Properties Company | Improved room air purifiers and filtration media |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5841297B2 (en) * | 1980-06-25 | 1983-09-10 | 旭化成株式会社 | Polymer compositions for open cell foams |
GB8709688D0 (en) * | 1987-04-24 | 1987-05-28 | Unilever Plc | Porous material |
DE4325879C3 (en) * | 1993-08-02 | 1999-05-20 | Depron Bv | Film made of a thermoplastic foam, process for its production and its use |
EP0822956B1 (en) * | 1995-04-27 | 2000-10-25 | The Dow Chemical Company | Extruded, open-cell microcellular foams, and their preparation process |
-
1999
- 1999-07-02 JP JP2000562127A patent/JP2002521188A/en active Pending
- 1999-07-02 BR BR9912425-4A patent/BR9912425A/en not_active Application Discontinuation
- 1999-07-02 KR KR1020017001234A patent/KR20010072094A/en not_active Withdrawn
- 1999-07-02 CN CN99807624A patent/CN1306452A/en active Pending
- 1999-07-02 AU AU48543/99A patent/AU4854399A/en not_active Abandoned
- 1999-07-02 WO PCT/US1999/015020 patent/WO2000006284A1/en not_active Application Discontinuation
- 1999-07-02 EP EP99932180A patent/EP1102618A1/en not_active Withdrawn
- 1999-07-02 CA CA002332815A patent/CA2332815A1/en not_active Abandoned
- 1999-07-28 AR ARP990103726A patent/AR019945A1/en unknown
- 1999-07-28 TW TW088112781A patent/TW469156B/en active
Also Published As
Publication number | Publication date |
---|---|
CN1306452A (en) | 2001-08-01 |
AR019945A1 (en) | 2002-03-27 |
EP1102618A1 (en) | 2001-05-30 |
BR9912425A (en) | 2001-04-17 |
KR20010072094A (en) | 2001-07-31 |
TW469156B (en) | 2001-12-21 |
JP2002521188A (en) | 2002-07-16 |
WO2000006284A1 (en) | 2000-02-10 |
CA2332815A1 (en) | 2000-02-10 |
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Legal Events
Date | Code | Title | Description |
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MK1 | Application lapsed section 142(2)(a) - no request for examination in relevant period |