Patent Application
20190201822
This application relates generally to water purification systems, and specifically to pathogen removing water filters.
Water filtration systems are used frequently on aircraft and other vehicles to ensure fresh water is available. There is market push to use more efficient microbiological water filter type filters for better water quality. Dual-ply filters, such as the filter disclosed in U.S. Pat. No. 8,678,201 B2, use pathogen-catching media plies in conjunction with pathogen-killing media plies to create water filters with longer operation lifespans and higher efficiency pathogen filtration. However, such dual-ply water filters need to bond two or more plies together, preferably without adhesives, to avoid significantly blocking the pore structure of the water filter.
A water filter media includes a pathogen-killing ply and a pathogen-catching ply that is thermally bound to an electrospun thermoplastic elastomer layer opposite a structural scrim layer. The pathogen-killing ply includes the structural scrim layer, and the electrospun thermoplastic elastomer layer is attached to the structural scrim layer. The electrospun thermoplastic elastomer layer contains biocides.
A water filter cartridge includes a filter media a first cap sealingly engaged with the filter media, and a second cap sealingly engaged with the filter media opposite the first cap. The filter media includes a pathogen-killing ply and a pathogen-catching ply thermally bonded to the pathogen-killing ply opposite a structural scrim layer. The pathogen-killing ply includes a biocide-loaded high temperature electrospun material on the structural scrim layer.
A method of making a water filter component includes electrospinning a biocide-loaded high temperature thermoplastic elastomer material onto a structural scrim layer to create a pathogen-killing ply, aligning the pathogen-killing ply with a pathogen-catching ply, and thermally bonding the pathogen-killing ply and the pathogen-catching ply together.
A water filter media that kills and catches pathogens typically includes multiple plies that accomplish different goals, such as catching pathogens or killing pathogens. These plies work more efficiently if they are joined together in water filter media. Often, adhesives are used to join multiple plies. However, these adhesives prevent or reduce water flow through multi-ply media. Alternatively, in this disclosure, a dual-ply media uses a thermal bond to secure multiple plies together without blocking water flow.
In this dual-ply water filter media, the pathogen-killing and pathogen-catching plies are attached with a spunbond porous scrim layer and are thermally bonded such that a high temperature thermoplastic elastomer layer in the pathogen-killing ply bonds to the pathogen-catching ply through the pores of the scrim layer between. Thus, the electrospun high temperature thermoplastic elastomer layer and scrim layer allow for water flow through the media. In contrast, traditional methods of adhesion have the potential to block pore and passages through which water would flow in filter media
Water tank 12 stores water needing to be filtered or purified. Pump 16 pumps water from tank 12 along water tank line 14 to pump line 18, and to water filter 20. In water filter 20, water is purified of pathogens. Once purified, water is flowed through output line 22 for use elsewhere in the vehicle. System 10 can optionally include more water tanks, pumps, valves, or other lines between water tank 12 and water filter 20. System 10 can also include other types of filters, such as particulate filters, upstream of water filter 20.
Housing 24 encloses cartridge 25 from an external environment. Housing 24 is connected to inlet 18A, which inputs water W into filter 20A (from water tank 12 in
Cartridge 25 includes first cap 26, second cap 28, and media 30, which includes pathogen-killing ply 32 and pathogen-catching ply 34. First and second caps 26, 28, are plastic caps which seal and encapsulate cartridge 25. First and second caps 26, 28, are circular in shape and seal to cylindrical media 30. In
Media 30 is a cylindrical shaped water filter media that both catches and kills pathogens. In
Pathogen-killing ply 32 is made of a pathogen-killing media, such as biocidal material. In water filter 20A, pathogen-killing ply 32 is made of electrospun layer 36 on scrim layer 40. Electrospun layer 36 is made of a high temperature thermoplastic elastomer and loaded with biocides. Electrospun layer 36 is created through electrospinning the biocide-loaded high temperature thermoplastic elastomer onto scrim layer 40. Scrim layer 40 is a polyester fabric that supports electrospun layer 36.
Electrospinning generally uses an electrical charge to draw very fine (typically on the micro or nano scale) fibers from a polymer solution. Electrospinning shares characteristics of both electrospraying and conventional solution dry spinning of fibers. The process is non-invasive and does not require the use of coagulation chemistry or high temperatures to produce solid threads from solution. Further, electrospinning from molten precursors has also been practiced in this art, which ensures that no solvent can be carried over into the final product.
A system for performing electrospinning generally includes a spinneret that is connected to a high-voltage direct current power supply, a syringe pump, and a grounded collector. Design of an applicable electro spinning process depends upon many factors, including, such as, molecular weight, molecular-weight distribution and architecture (e.g., branched, linear etc.) of the fibers, solution properties (e.g., viscosity, conductivity, and surface tension), electric potential, flow rate and concentration, distance between the capillary and collection screen, ambient parameters (e.g., temperature, humidity and air velocity in the chamber), and motion of target screen (collector).
The electrospun material used for pathogen-killing ply 32 can include a thermoplastic elastomer such as thermoplastic polyurethanes (TPU), styrenic block copolymers (TPS (TPE-s)), thermoplastic polyolefinelastomers (TPO (TPE-o)), thermoplastic vulcanizates (TPV (TPE-v or TPV)), thermoplastic copolyester (TPC (TPE-E)), thermoplastic polyamides (TPA (TPE-A)), or other thermoplastic elastomers with high melting temperatures such that the material does not completely liquefy during thermal lamination.
Here, pathogen-killing ply 32 includes an electrospun high temperature thermoplastic elastomer that is pre-loaded with biocides. A biocide a chemical substance or microorganism which exerts a controlling effect on any harmful organism by chemical or biological means. The biocidal agents can be, for example, sodium dichloro-s-triazinetrione (dihydrate or anhydrous; “dichlor”), trichloro-s-triazinetrione (“trichlor”), halogenated hydantoin compounds, nanoparticles of copper and its alloys (e.g., brasses, bronzes, cupronickel, copper-nickel-zinc, etc.), silver nanoparticles and its derivativesor, quaternary ammonium compounds, and silica nanoparticles chemically bound with silyl quaternary amine.
Scrim layer 40 is typically a highly porous spunbond thin fabric onto which the high temperature elastomer (loaded with biocides) is spun. Scrim layer 40 alloys for easier handling of thin electrospun layer 36. Additionally, electrospun layer 36 can be attached scrim layer 38, which lays between electrospun layer 36 and pathogen-catching ply 34. Scrim layer 38 is also a spunbond thing fabric such as a polyester fabric. The porous nature of scrim layer 38 allows electrospun layer 36 to seep through pores in scrim layer 38 to attach to pathogen-catching ply 34, creating a thermal bond between electrospun layer 36, scrim layer 38, and pathogen-catching ply 34. In media 30, scrim layer 38 bonds to both pathogen-catching ply 34 and pathogen-killing ply 32. Scrim 38 is preferred, but can be optional in some embodiments where electrospun layer 36 is thermally bonded directly onto pathogen-catching ply 34.
The melting temperature of the thermoplastic elastomer electro spun onto pathogen-killing ply 32 should be higher than, but close to the laminating temperature used to connect plies 32, 34, through scrim layer 38. Thus, the thermoplastic elastomer will not melt, but will be softened to facilitate thermal bonding through the porous structure of scrim layer 38. Scrim layer 38 (which typically is spunbond) is thermally bonded to both plies providing additional attachment.
Pathogen-catching ply 34 is made of a pathogen-catching medium. Typically, pathogen-catching ply 34 can be alumina or glass fiber fabric optionally with an activated carbon component, or other electropositive or electroadsorptive material that can catch pathogens in water W. An electropositive material can include, for example, pseudoboehmite AlO(OH), or alumina. Alumina particles are electroadsorptive, and are able to catch pathogen particles via the inherent charge field extending across the void volume of the pores of glass fiber fabric. The pathogen-catching ply can alternatively be size exclusion capability of microfiltration (MF) or ultrafiltration (UF) membranes or nanofiltration (NF), or electroadsorptive media. An example of an appropriate electroadsorptive media is Disruptor® media (available from AHLSTROM MUNKSJÖ). Disruptor® medias have non-woven glass fibers fabric, where glass fibers are coated with nano alumina fibers.
Media 30 has several benefits. First, the use of a high temperature elastomer in electrospun layer 36 allows for creation of a thermal bond to pathogen-catching ply 34 without significantly affecting pore size or structure in media 30. In contrast, traditional adhesive block pore structures in filter media and prevent water flow. This often results in significantly increasing the water pressure drops. Thus, the flow rate of water through pathogen-killing ply 32 and pathogen-catching ply 34 is minimally reduced. Additionally, pathogen-killing ply 32 does not shed or create debris in water running through filter 20. Pathogen-killing ply 32 is made of a high strength continuous elastomer fibers to form a fabric by electrospinning, so fibers are less likely to break off and enter the water stream to prevent escape of the biocide-containing debrides.
Media 30 can optionally include external scrim layer 42 which can be made of a polyester fabric. Scrim layer 42 provides surface protection to pathogen-catching ply 34 within cartridge 25. In some embodiments, pathogen-catching ply 34 can be bonded to scrim layer 42, or come prepared on scrim layer 42 prior to assembly of media 30. In these embodiments, scrim layer 42 aids in handling of pathogen-catching ply 34. Both scrim layers 38 and 42 can optionally be pre-laminated onto pathogen-catching ply 34 before pathogen-killing ply 32 is bonded to the rest of media 30, or all layers 32-42 can be simultaneously thermally laminated in media 30.
Media 30 is typically cylindrical in shape such that media 30 can seal with caps 26, 28, to form cartridge 25. Additionally, media 30 can include additional plies, such as additional pathogen-killing or pathogen-catching plies, or chemical or dirt retaining plies that can be thermally bonded in a similar fashion. In
In cartridge 25 of filter 20A, water flows in the direction of arrows W, entering from inlet 18A (shown in
Alternatively, water flow can be reversed. In
The layers are overlaid and thermally bound to create the final media 30 in
The proposed multi-ply water filter media includes a method of bonding pathogen-killing plies containing electro spun high temperature thermoplastic elastomers to pathogen-catching plies with thermal bonding techniques. This allows for bonding of plies without using adhesive, and does not clog or block water paths through filter media, ensuring water filter efficiency and preventing drops in water pressure. Additionally, the use of high strength electrospun elastomers prevents biocidal debris formation, as high strength electrospun elastomer loaded with biocides do not shed like other brittle fabrics or short fiber fabrics used in water filter systems. This is because that the electrospinning fibers are known to have almost perfect non-stop fibers and the elastomer provides stretching capability to resist fibers damages by usual handling.
The following are non-exclusive descriptions of possible embodiments of the present invention.
A water filter media includes a pathogen-killing ply and a pathogen-catching ply that is thermally bound to an electrospun thermoplastic elastomer layer opposite a structural scrim layer. The pathogen-killing ply includes the structural scrim layer, and the electrospun thermoplastic elastomer layer is attached to the structural scrim layer. The electrospun thermoplastic elastomer layer contains biocides.
The media of the preceding paragraph can optionally include, additionally and/or alternatively, any one or more of the following features, configurations and/or additional components:
The electrospun thermoplastic elastomer layer is selected from the group consisting of a thermoplastic elastomer polyurethane, a styrenic block copolymer, a thermoplastic polyolefinelastomer, a thermoplastic copolyester, and a thermoplastic polyamide.
The biocides are selected from the group consisting of sodium dichloro-s-triazinetrione, trichloro-s-triazinetrione, halogenated hydantoin compounds, quaternary ammonium compounds, silica nanoparticles chemically bound with silyl quaternary amine, copper, copper alloys, silver, silver nanoparticles, and silver derivatives.
The pathogen-catching ply is selected from the group consisting of electroadsorptive nano-alumina fabric, and glass fiber fabric.
The pathogen-catching ply further comprises activated carbon.
The pathogen-catching ply is selected from the group consisting of microfiltration membranes, ultrafiltration membranes, and nanofiltration membranes.
The water filter media includes a middle scrim layer through which the pathogen-catching ply is thermally bonded to the pathogen-killing ply.
The middle scrim layer is a non-woven fabric selected from the group consisting of nylon, polyester, polypropylene, and combinations thereof.
The water filter media includes an external scrim layer attached to the pathogen-catching ply opposite the pathogen-killing ply.
A water filter cartridge includes a filter media a first cap sealingly engaged with the filter media, and a second cap sealingly engaged with the filter media opposite the first cap. The filter media includes a pathogen-killing ply and a pathogen-catching ply thermally bonded to the pathogen-killing ply opposite a structural scrim layer. The pathogen-killing ply includes a biocide-loaded high temperature electrospun material on a structural scrim layer.
The water filter cartridge of the preceding paragraph can optionally include, additionally and/or alternatively, any one or more of the following features, configurations and/or additional components:
The water filter cartridge includes a porous scrim layer between the pathogen-killing ply and the pathogen-catching ply.
The high temperature thermoplastic electro spun material is selected from the group consisting of a thermoplastic elastomer polyurethane, a styrenic block copolymer, a thermoplastic polyolefinelastomer, a thermoplastic copolyester, and a thermoplastic polyamide.
The pathogen-catching ply comprises nano-alumina and activated carbon.
The filter media further comprises one or more external scrim layers attached to the pathogen-killing ply or the pathogen-catching ply.
A method of making a water filter component includes electrospinning a biocide-loaded high temperature elastomer material onto a scrim layer to create a pathogen-killing ply, aligning the pathogen-killing ply with a pathogen-catching ply, and thermally bonding the pathogen-killing ply and the pathogen-catching ply together.
The method of the preceding paragraph can optionally include, additionally and/or alternatively, any one or more of the following features, configurations and/or additional components:
Thermally bonding the pathogen-killing ply and the pathogen-catching ply together comprises laminating.
Thermally bonding the pathogen-killing ply and the pathogen-catching ply together comprises using an autoclave.
The method includes sealing the pathogen-killing ply and the pathogen-catching ply to a cap.
Sealing the pathogen-killing ply and the pathogen-catching ply to a cap comprises thermal sealing.
Sealing the pathogen-killing ply and the pathogen-catching ply to a cap comprises using an adhesive.
While the invention has been described with reference to an exemplary embodiment(s), it will be understood by those skilled in the art that various changes may be made and equivalents may be substituted for elements thereof without departing from the scope of the invention. In addition, many modifications may be made to adapt a particular situation or material to the teachings of the invention without departing from the essential scope thereof. Therefore, it is intended that the invention not be limited to the particular embodiment(s) disclosed, but that the invention will include all embodiments falling within the scope of the appended claims.
