A METHOD FOR PREPARING A COMPOSITE FILTER MEDIUM AND THE COMPOSITE FILTER MEDIUM OBTAINED WITH THIS METHOD
20220339567 · 2022-10-27
Inventors
- Roberto MOMENTE (Appiano Gentile, IT)
- Carmine LUCIGNANO (Appiano Gentile, IT)
- Martina SIMONE (Appiano Gentile, IT)
- Paolo CANONICO (Appiano Gentile, IT)
Cpc classification
B01D2239/0442
PERFORMING OPERATIONS; TRANSPORTING
B01D2239/0428
PERFORMING OPERATIONS; TRANSPORTING
B01D2239/0421
PERFORMING OPERATIONS; TRANSPORTING
H04M1/18
ELECTRICITY
International classification
Abstract
A method for preparing a composite filter medium (1), comprising a step of forming a first filter medium (8) through deposition of nanofibers (4) on a base fabric (2) through an electrospinning process and a step of covering said filter medium (1) by plasma deposition of a coating (7) on said first filter medium (8) in a vacuum chamber (9). According to the invention, after the electrospinning process and before the plasma deposition of the coating (7), a degassing step of the base fabric (2) and of the nanofibers (4) forming the aforementioned first filter medium (8) is provided inside the same chamber (9). With respect to the known filter media, that of the invention offers the advantage of maintaining the desired level of water and oil repellency, due to the formation of a completely polymerized coating strongly adhering to the surface of the base fabric and of the nanofibers.
Claims
1. A method for preparing a composite filter medium (1), comprising a step of forming a first filter medium (8) through deposition of nanofibers (4) on a base fabric (2) by means of an electrospinning process and a step of covering said filter medium (1) by plasma deposition of a coating (7) on said first filter medium (8) in a vacuum chamber (9), characterized in that said method provides, after said electrospinning process and before said plasma deposition of the coating (7), a degassing step of the base fabric (2) and the nanofibers (4) forming the aforementioned first filter medium (8) inside the same chamber (9).
2. The method according to claim 1, characterized in that, during said degassing step, the aforementioned chamber (9) is brought to an internal pressure value of between 5 and 250 mTorr.
3. The method according to claim 1, characterized in that, during said degassing step, an exposure time in the chamber from 5 seconds to 5 minutes is ensured for the material.
4. The method according to claim 1, characterized in that, after the aforementioned degassing step and before said plasma deposition of the coating (7), it also provides a step of formation of irregularities on the surface of said base fabric (2) and of the aforementioned nanofibers (4), through plasma treatment of said first filter medium (8) obtained in the previous degassing step, carried out in said chamber (9) in the presence of a carrier gas and without any polymer-containing gases.
5. The method according to claim 4, characterized in that the aforementioned carrier gas is selected from nitrogen, helium, argon or oxygen.
6. The method according to claim 5, characterized in that the aforementioned plasma treatment is performed in the chamber (9) at a pressure of 10-400 mTorr, with an electrode power of 100-2000 W and with an exposure time of between 5 seconds and 5 minutes.
7. The method according to claim 1, characterized in that the electrospinning process involves the extrusion of polymer dissolved in a suitable solvent, by means of a nozzle (5) and subsequent stretching of the fibers between the nozzle itself and an electrode, thus obtaining a deposition of nanometric fibers on the base fabric, suitably interposed between the nozzle and the electrode, the filter medium (8) thus obtained being subsequently subjected to a surface treatment through plasma deposition of a polymeric layer (7) of nanometric thickness on the exposed surfaces of the base fabric (2) and of the nanofiber layer (4), obtaining the aforementioned composite filter medium (1) in which the external surfaces of the monofilaments (3) of the base fabric (2) and of the aforementioned nanofibers (4) are coated with said polymeric layer (7).
8. The method according to claim 7, characterized in that the aforementioned plasma deposition treatment comprises the creation of a vacuum of 10-50 mTorr, an electrode power of 150-350 W and an exposure time of 0.5-6 minutes.
9. A method for preparing a composite filter medium (1), comprising a step of forming a first filter medium (8) through deposition of nanofibers (4) on a base fabric (2) by means of an electrospinning process and a step of covering said filter medium (1) by plasma deposition of a coating (7) on said first filter medium (8) in a vacuum chamber (9), characterized in that said method provides, after said electrospinning process and before said plasma deposition of the coating (7), a step of forming irregularities on the surface of said base fabric (2) and of said nanofibers (4), through plasma treatment of said first filter medium (8) carried out in said chamber (9) in the presence of a carrier gas and without any polymer-containing gases.
10. A composite filter medium, of the type comprising a base fabric (2) on which nanofibers (4) are deposited, characterized in that said base fabric and the aforementioned nanofibers are covered with a nanometric coating layer (7), applied by means of a plasma process, the base fabric (2) and the nanofibers (4) having nanogrooves obtained through plasma treatment in the presence of a carrier gas and without any polymer-containing gases.
11. The filter medium according to claim 10, characterized in that the aforementioned coating (7) is formed by a film having a thickness of up to 500 nm, preferably with a thickness of 15-60 nm.
12. The filter medium according to claim 10, characterized in that the aforementioned coating (7) is a coating based on fluorocarbon acrylates with water- and oil-repellent properties.
13. The filter medium according to claim 10, characterized in that said monofilaments (3) are made starting from monofilament of polyester, polyamide, polo ypropylene, polyether sulfone, polyimide, polyamide imide, polyphenylene sulfide, polyether ether ketone, polyvinylidene fluoride, polytetrafluoroethylene, aramid.
14. The filter medium according to claim 10, characterized in that the aforementioned base fabric (2) has a mesh opening of 2500-5 microns.
15. The filter medium according to claim 10, characterized in that the aforementioned base fabric (2) has a textile construction of 4-300 threads/cm, thread diameter of 10-500 microns, weave with a weight of 15-300 g/m.sup.2 and thickness of 18-1000 microns.
16. The filter medium according to claim 10, characterized in that the aforementioned nanofibers (4) are nanofibers of polyester, polyurethane, polyamide, polyimide, polypropylene, polysulfone, polyether sulfone, polyamide imide, polyphenylene sulfide, polyether ether ketone, polyvinylidene fluoride, polytetrafluoroethylene, alginate, polycarbonate, PVA (polyvinyl alcohol), PLA (polylactic acid), PAN (polyacrylonitrile), PEVA (polyethylene vinyl acetate), PMMA polymethyl methacrylate), PEO (polyethylene oxide), PE (polyethylene), PVC, PI or polystyrene.
17. The filter medium according to claim 10, characterized in that said nanofibers (4) have a diameter of between 50 nm and 700 nm, preferably they are PVDF (polyvinylidene fluoride) nanofibers with a diameter ranging from 75 to 200 nm.
18. Use of the filter medium according to one or more of the preceding claims for the protection of electroacoustic components in mobile phones.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0013] These and other objects, advantages and features will be apparent from the following description of a preferred embodiment of the method and the filter medium according to the invention illustrated by way of a non-limiting example in the figures in the attached drawings.
[0014] In these:
[0015]
[0016]
[0017]
[0018]
[0019]
[0020]
DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0021] The composite filter medium of the invention, indicated as a whole by the number 1 in
[0022] The base fabric used in the preparation of the composite filter medium of the invention is selected from a wide range of synthetic monofilament fabrics, which differ in the chemical nature of the monofilament used for weaving, such as polyester, polyamide, polypropylene, polyether sulfone, polyimide, polyamide imide, polyphenylene sulfide, polyether ether ketone, polyvinylidene fluoride, polytetrafluoroethylene, aramid. Also suitable for the invention are base fabrics with textile construction of 4-300 threads/cm, thread diameter of 10-500 microns, weave with a weight of 15-300 g/m.sup.2 and thickness of 18-1000 microns. For finishing and further surface treatments, in addition to metallization, use can be made of washed and heat-set “white” fabric, colored fabric, fabric subjected to plasma treatment, hydrophobic, hydrophilic, antibacterial, antistatic fabric and the like. Preferred for the invention is a polyester monofilament fabric, with 48 threads/cm, diameter 55 μm, mesh opening of the base fabric of 153 μm.
[0023] Suitable for the invention are nanofibers 4 of polyester, polyurethane, polyamide, polyimide, polypropylene, polysulfone, polyether sulfone, polyamide imide, polyphenylene sulfide, polyether ether ketone, polyvinylidene fluoride, polytetrafluoroethylene, alginate, polycarbonate, PVA (polyvinyl alcohol), PLA (polylactic acid), PAN (polyacrylonitrile), PEVA (polyethylene vinyl acetate), PMMA polymethyl methacrylate), PEO (polyethylene oxide), PE (polyethylene), PVC, PEI, PUR and polystyrene. These nanofibers can have a diameter of between 50 nm and 700 nm. PVDF (polyvinylidene fluoride) nanofibers with a diameter ranging from 75 to 200 nm are preferred.
[0024] As illustrated in
[0025] The composite filter medium obtained in this way is then subjected to a surface treatment by plasma deposition of a polymeric layer 7 of nanometric thickness on the exposed surfaces of the fabric 2 and of the nanofiber layer 4, completely covering the external surfaces of the monofilaments 3 of the base fabric 2 and of the aforementioned nanofibers 4 (
[0026] As shown in
[0027] Preferred for the invention are gases based on fluorocarbon acrylates, in particular, heptadecafluorodecyl acrylate, perfluorooctylacrylate and the like. Advantageous for the invention are the gases forming by plasma treatment a deposit of fluorocarbon acrylates, due to their water- and oil-repellent properties.
[0028] In the plasma treatment described above, a carrier gas is also used, for example the type described in WO2011089009A1.
[0029] The aforementioned plasma treatment involves the creation of a vacuum of 10-50 mTorr, an electrode power of 150-350 W and an exposure time of 0.5-6 minutes.
[0030] The coating deposited by means of plasma technology can have a thickness of up to 500 nm and, due to the particular technology used, has the structure of a continuous film, capable of coating even 3D surfaces like those of a fabric. Depending on the chemical compound used, the aforementioned coating can have various peculiar characteristics, such as hydrophobicity, oleophobicity, hydrophilicity and antistaticity.
[0031] Preferred for the invention are the coatings obtained starting from the following chemical compounds in the starting gases:
[0032] 1H,1H,2H,2H-HEPTADECAFLUORODECYL ACRYLATE (CAS #27905-45-9, H.sub.2C═CHCO.sub.2CH.sub.2CH.sub.2(CF.sub.2).sub.7CF.sub.3)
[0033] 1H,1H,2H,2H-PERFLUOROOCTYL ACRYLATE (CAS #17527-29-6, H.sub.2C═CHCO.sub.2CH.sub.2CH.sub.2(CF.sub.2).sub.5CF.sub.3)
[0034] The thickness of the coating 7 is 15-60 nm, suitable to prevent it from excessively narrowing the pores that the composite filter medium 1 forms in both the fabric 2 and the nanofibers 4, which would hinder the free passage of sound.
[0035] Tests were carried out on composite filter medium 8, as obtained from the electrospinning process of
[0036] In particular, the aforementioned filter medium 8 is formed by a weft and warp fabric made of synthetic monofilament 3 (for example of polyester), on which nanofibers 4, also made of synthetic material (for example polyester), have been deposited, in order to obtain an acoustic impedance of 25 MKS Rayls, measured with the Textest instrument or similar for measuring the acoustic impedance/air permeability.
[0037] After plasma treatment of the filter medium 8, it can be observed, on the composite filter medium 1 of the invention, that the acoustic impedance remains unchanged at values of 25 MKS Rayls. The air permeability value of 5,200 l/m.sup.2s at a pressure of 200 Pa and the filtration efficiency also remain unchanged.
[0038] On the other hand, a considerable increase is observed both in the angle of contact with water (from 50° to 130°), and in the angle of contact with oil (from 50° to 120° for an oil with corn oil having a surface tension of 32 mN/m), where the angle of contact is measured on a drop of water or oil with the nanofibers 4, using the sessile method with Kruss instruments (drop deposition and measurement of the angle of contact by means of high resolution camera).
[0039] Declogging Test
[0040] In order to provide evidence of the observations set out above, a test method was developed with a view to numerically quantifying the energy necessary to remove the oil deposited on the surface of the composite filter medium of the invention.
[0041] This test was carried out with a porometer (PMI 1200, manufactured by PMI), an instrument that uses capillary flow porometry to determine the bubble point, the minimum pore size and the distribution of the pore size on the sample tested. Capillary flow porometry, or simply porometry, is based on an extremely simple principle: measuring the pressure of a gas necessary to force the passage of a wetting liquid through the pores of the material. The pressure at which zo the pores empty is inversely proportional to the size of the pores themselves. Large pores require low pressures while small pores require high pressures.
[0042] The test consists in cutting the sample to be analyzed and placing it inside the test chamber. Subsequently the sample is held in position by means of O-rings, in such a way as to be sure there are no lateral air leaks. Once the chamber is closed, the air permeability of the filter medium is measured, obtaining a curve that puts the air flow through the sample in relation with the pressure drop measured across the filter medium (dry curve in the graph in
[0043] In the specific case, in order to determine the oil repellency/removal capacity, this test was carried out but using corn oil (surface tension 32 mN/m) in place of the test liquid.
[0044] The graph in
[0045] According to the invention, it has now surprisingly been discovered that, by adding to the method described above a preliminary step of degassing the material forming the monofilament 3 and the nanofibers 4 of the composite filter medium 8 to be treated in the vacuum chamber and a subsequent plasma treatment, performed prior to the step of formation of the coating 7, complete polymerization and strong adhesion of the coating subsequently deposited on the monofilament forming the base fabric and on the nanofibers are achieved.
[0046] In particular, according to the invention, prior to the step of formation of the plasma coating 7, a degassing step of the filter medium 8 obtained in the previous electrospinning process is carried out in the chamber 9, so as to bring the pressure in the chamber 9 to a value of 5-250 mTorr. For this purpose, depending on the size, weight and hygroscopicity of the material to be treated, a degassing step should be provided having an exposure time of the material typically in a range from 5 seconds to 5 minutes. Of course, once the proper exposure time, allowing a complete drying of the media, is defined, i.e. a time ensuring a stable vacuum degree in the subsequent coating step, the correct speed for the degassing step shall be set, depending on the exposed area within the chamber. Such area is defined by the distance between unwinding and winding cylinders and by the electrode size. In particular, if a material is packaged in rolls, it will be continuously unwound and rewound inside the chamber 9 at a speed of between 0.1 and 50 m/min depending on the moisture content of the material. An opening, suitably controlled by a system of valves, will be provided in the chamber 9 so that the gases to be eliminated can be vented.
[0047] According to the invention, the preliminary check on the aforementioned pressure values will allow the moisture contained in the material to be treated in the chamber 9 to be removed completely so as to allow the desired polymerization pressure of the coating 7 on the surface of the base fabric and the nanofibers to be reached, in the subsequent step of formation of said coating.
[0048] Furthermore, according to the invention, after the degassing treatment described above and again prior to the step of formation of the coating 7, the surfaces of the monofilament 3 forming the base fabric 2 and of the nanofibers 4 are reactivated in the chamber 9, by means of a plasma treatment performed in the chamber 9 maintained at a pressure of 10-400 mTorr, with an electrode power in a range of 100-2000 W and an exposure time in a range of 5 seconds to 5 minutes, with a carrier gas, preferably selected from nitrogen, helium, argon and oxygen. Depending on the gas used, the exposure time and the power, a more or less marked etching effect will be obtained, resulting in the formation of a nanometric/micrometric roughness on the surface to be treated.
[0049] In this step there is no formation of any coating on the treated surfaces, as the polymeric monomer is not present. On the contrary, the ions coming from the carrier gas, duly energized by the plasma, impact with some energy on the surface of the substrate, creating nanogrooves and consequently nanometric roughness, which favors the grip and adhesion of the polymer coating 7 to the surface of the monofilament 3 and the nanofibers 4, contributing significantly to the repellent action of the filter medium towards water and oily liquids.
[0050] The results offered by the filter medium made with the process of the invention are shown in the following table, the values of which were measured on a filter medium having a layer 7 of polymeric material, obtained by performing the plasma treatment for the formation of the latter after: [0051] a degassing step, carried out by keeping the material to be treated inside the chamber 9 for a time of 30 seconds, suitable to ensure a stable pressure of 25 mTorr in the subsequent treatment; [0052] and, subsequently, a step of plasma treatment of the material to be coated, carried out in the presence of helium as a carrier gas, with a vacuum of 150 mTorr, an electrode power of 600 W and an exposure time of 1 minute:
TABLE-US-00001 Minimum angle of contact required Angle of contact for the application with oil (°) (°) Electrospinning process + 130-135 110 plasma deposition without degassing and without plasma pretreatment (known technique) Electrospinning process + 115 110 degassing + preliminary plasma treatment + deposition of plasma coating (invention)
[0053] From these results it can be seen how the polymeric coating 7 formed in the vacuum chamber 9 after a degassing step and a preliminary plasma treatment, ensures the filter medium of the invention a very high angle of contact with oil (>110°), and a much higher adhesion level to the substrate than the minimum required.
[0054] In the invention as described above and illustrated in the figures in the attached drawings, changes may be made in order to produce variants which nevertheless fall within the scope of the appended claims.
[0055] In particular, when the filter medium is made starting from slightly hygroscopic materials and is to be subjected to the plasma deposition process, it is possible to perform the reactivation step alone by plasma treatment and with a carrier gas, again selected from nitrogen, helium, argon and oxygen. In fact, for this type of slightly hygroscopic materials, the above-described preliminary degassing step can be omitted.