Desalination device and method of manufacturing such a device
12030795 ยท 2024-07-09
Assignee
Inventors
Cpc classification
B01D61/428
PERFORMING OPERATIONS; TRANSPORTING
B01D61/4281
PERFORMING OPERATIONS; TRANSPORTING
Y02A20/131
GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
C02F1/4604
CHEMISTRY; METALLURGY
C02F2001/46138
CHEMISTRY; METALLURGY
International classification
B01D61/42
PERFORMING OPERATIONS; TRANSPORTING
Abstract
A device (10) for capacitive deionization of an aqueous media containing dissolved ion species, said device comprising a cell with a first primary electrode (2) and a second primary electrode (3) arranged opposite the first primary electrode (2) and preferably separated by at least one non-conductive spacer (4, 4). A third electrode (7) is arranged between the first and the second electrode. The third electrode (7) is grounded whereas the first and the second electrodes are polarized versus the grounded third electrode.
Claims
1. A capacitive deionization device (10) comprising a first electrode (2) and a second electrode (3), the second electrode (3) opposing the first electrode (2), wherein the first electrode (2) and the second electrode (3) are separated from each other by at least one electrically non-conductive spacer (4, 4) arranged between the first electrode and the second electrode, wherein the device further comprises a third electrode (7) between the first electrode (2) and the second electrode (3), the third electrode (7) allowing substantially unrestricted flow of aqueous media from a first side of the third electrode facing the first electrode (2) to a second side of the third electrode facing the second electrode (3), wherein the third electrode (7) is electrically grounded, and the first electrode (2) and the second electrode (3) are polarizable with opposite charges with respect to the third electrode (7), wherein each one of the first electrode (2), the second electrode (3) and the third electrode (7) is made of a chemically inert and flexible material, and wherein the first electrode (2), the second electrode (3), and the third electrode (7) are arranged in a spiral form around a longitudinal and/or common central axis such that the first electrode (2), third electrode (7) and second electrode (3) are periodically repeated along the radius in a plane perpendicular to the longitudinal and/or central axis and jointly form a substantially cylindrical structure.
2. The device according to claim 1, wherein the third electrode comprises a circumferential outer peripheral edge which has substantially the same circumferential size and shape as a circumferential peripheral edge of the first electrode and/or a circumferential peripheral edge of the second electrode.
3. The device according to claim 1, wherein the third electrode has a geometrical configuration of a ring.
4. The device according to claim 3, wherein the ring is a circular ring, a rectangular ring, a square ring, or a octahedral ring.
5. The device according to claim 1, wherein the third electrode is arranged at substantially equal distances from the first electrode and the second electrode.
6. The device according to claim 1, wherein the third electrode is made of carbon or a carbon-based material.
7. The device according to claim 6, wherein the carbon or a carbon-based material comprises an activated carbon cloth, a graphite plate or one or more graphene sheets.
8. The device according to claim 1, wherein the third electrode is arranged in the form of a coating on a flexible electrically non-conductive spacer.
9. The device according to claim 1, wherein the third electrode is embedded in a flexible monolithic electrically non-conductive spacer.
10. The device according to claim 1, wherein the third electrode is printed on a flexible electrically non-conductive spacer.
11. The device according to claim 9, wherein the flexible monolithic electrically non-conductive spacer is in direct contact with the first electrode at a first side surface of the monolithic spacer, and in direct contact with the second electrode at a second side surface of the monolithic spacer.
12. The device according to claim 1, further comprising a substantially cylindrical housing in which the substantially cylindrical structure is arranged, an inlet at a first end surface of the housing and an outlet at a second end surface of the housing, wherein each of the electrodes comprises at least one current collector extending out from the housing through one of the first end surface and the second end surface.
13. A capacitive deionization arrangement comprising a plurality of capacitive deionization devices, wherein at least one of the plurality of capacitive deionization devices is a capacitive deionization device according to claim 1.
14. A method of deionizing an aqueous media comprising using a capacitive deionization device according to claim 1 for removing charged species from the aqueous media.
15. A method of deionizing an aqueous media comprising using an arrangement according to claim 13 for removing charged species from the aqueous media.
16. A method of manufacturing a capacitive deionization device, the method comprising providing a first electrode, arranging a third electrode on a first side of the first electrode and arranging a second electrode on a second side of the third electrode, wherein the third electrode allows free flow of aqueous media from a first side surface of the third electrode facing the first electrode to a second side surface of the third electrode facing the second electrode, providing a grounded connection to the third electrode and connecting the first electrode and the second electrode such that they are polarizable with opposite charges with respect to the third electrode, wherein each one of the first electrode, the second electrode and the third electrode is made of a chemically inert and flexible material, and rolling the first electrode, third electrode and second electrode in a spiral form around a common longitudinal and/or central axis such that the first electrode, third electrode and second electrode are periodically repeated along a radius in a plane perpendicular to the longitudinal and/or central axis and jointly form a substantially cylindrical structure.
17. The method according to claim 16, further comprising arranging the rolled substantially cylindrical structure into a substantially cylindrical housing comprising a first end surface and a second end surface, arranging an inlet at the first end surface of the housing and an outlet at the second end surface of the housing, and arranging for each of the electrodes at least one current collector extending out through the housing through at least one of the first end surface and the second end surface.
18. The method according to claim 16, wherein the first electrode, third electrode and second electrode are arranged around a perforated pipe having an open end and a closed end, said open end of the pipe serving as inlet or outlet for aqueous media to be subjected to capacitive deionization.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1) The invention and embodiments thereof will now be described, by way of non-limiting examples, with reference to the accompanying drawings, in which:
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DETAILED DESCRIPTION
(18) The present invention will be described below with reference to the accompanying drawings and certain exemplifying embodiments. The invention is however not limited to the embodiments shown, but can be varied within the scope of the appended claims. Moreover, the drawings shall not be considered to necessarily be drawn to scale as some features may be exaggerated in order to more clearly illustrate the features of the device(s) or the details thereof.
(19) Before the present invention is described, it is to be understood that the terminology employed herein is used for the purpose of describing particular embodiments only and is not intended to be limiting, since the scope of the present invention will be limited only by the appended claims and equivalents thereof.
(20) It must be noted that, as used in this specification and the appended claims, the singular forms a, an, and the include plural referents unless the context clearly dictates otherwise.
(21) In the present disclosure, the term electrode surface area shall be considered to mean the geometrical surface area of an electrode in the plane of the electrode, irrespective of whether the plane of the electrode is a planar plane or has another configuration such as undulating or cylindrical. This is in contrast to the term specific surface area which shall be considered to mean the total surface area per unit of mass.
(22) Furthermore, in the present disclosure the term electrically non-conductive is used. It should be recognised that all materials have a certain electrical conductivity even if it is very low. By way of example only, even a material considered to be an isolator will have a certain electrical conductivity. Thus, an electrically non-conductive material or an electrically non-conductive material constituent component shall in the present disclosure be understood to mean a material or constituent component having such a low electrical conductivity that the electrical conductivity therein is so low that there will be essentially no electrical conductivity therein when the device according to the present invention is used as intended during the operation thereof. In other words, electrically non-conductive shall be considered to mean a negligible electrical conductivity when used as intended.
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(24) The first and second electrodes 2, 3 are usually separated by a first electrically non-conductive spacer 4. The device further optionally comprises more than one non-conductive spacer, as illustrated in
(25) The device 1 further comprises a first current collector 5 connected to the first electrode 2, and a second current collector 6 connected to the second electrode 3. In a conventional CDI device, the cathode is generally grounded and the anode is polarized with reference to the cathode. The electrodes are connected via the respective current collectors to a DC power source (not shown) in order to enable polarization of the electrodes.
(26) During operation of the CDI device, anions are attracted to the positive electrode and absorbed in the positive electrode. Simultaneously, cations are attracted to the negative electrode and adsorbed therein. Thereby, the ions are removed from the aqueous media present between the electrodes.
(27) In any CDI device, ions are attracted in response to the potential mediated electric field lines generated at the electrode surfaces. Thus, the ion removal and capacity is proportional to the distribution and strength of the lines of field.
(28) In contrast to the prior art as shown in
(29) Additionally, the third electrode ensures the electric fields generated between the primary electrodes converge from both sides at the central third electrode, thereby improving the field distribution between the primary electrodes. Improved field distribution leads to efficient power utilization and improved ion removal capacity for the CDI device.
(30) The third electrode is configured to allow free flow of aqueous media from a first side of the third electrode to a second side of the third electrode. The first side surface of the third electrode is in the present disclosure considered to mean the side of the third electrode facing the first electrode. Correspondingly, the second side of the third electrode is in the present disclosure considered to mean the side of the third electrode facing the second electrode. In the present disclosure, a free or unrestricted flow of aqueous media from a first side to a second side is considered to mean that aqueous media can pass through the third electrode without any significant pressure drop.
(31) This is in contrast to for example the first and second electrodes, through which aqueous media is allowed to pass but wherein this would result in a pressure drop of the aqueous media from a first side of the electrodes to a second side of the electrodes. In other words, the third electrode is not intended to cause any physical division of water flow between the different sides of the third electrode. However, the third electrode provides an electrical division of the volume between the first electrode and the second electrode.
(32) It is preferred that the third electrode is arranged at equal distances from the first electrode and the second electrode, i.e. midway between the first electrode and the second electrode. This ensures that the potential will be divided equally between the first electrode and the second electrode with respect to the third electrode, and thereby enables an essentially symmetrical adsorption of charge species at the primary electrodes. However, it should be noted that a certain tolerance as to the position of the third electrode with respect to the first and second electrodes is possible while still obtaining a sufficiently good result.
(33) Thus, the third electrode is preferably arranged at a distance which is 40-60% of the distance between the first electrode and the second electrode if a symmetric cation and anion removal is desired. When discussing a distance between the first electrode and/or the second electrode to the third electrode, it shall in the present disclosure be considered to mean a distance between the surface of the first electrode and/or second electrode to a central plane of the third electrode, the central plane of the third electrode being parallel to the side surfaces of the third electrode.
(34) According to an alternative aspect, the capacitive deionization device is used in applications where preferential anion or cation removal is desired. Therefore, depending on the desired ion removal, the distance of the third electrode with respect to the first and second electrodes is flexible. In general, the third electrode is arranged at a distance which is 10-90% of the distance between the first electrode and the second electrode, while still maintaining acceptable pressure drop and fluid flow permeability. For example, if the third electrode is closer to the first surface of the first electrode then the electric field between the first and third electrode is stronger than the third and second electrode, leading to preferential anion removal if the first electrode is positive and vice versa. Thus the third electrode can provide a means to preferentially remove either positively or negatively charged species without chemical modification of the first, second or third electrodes.
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(36) In the CDI device according to
(37) In contrast to the CDI device 1 illustrated in
(38) As shown in
(39) The third electrode 7 preferably has the geometrical configuration of a substantially planar ring, such as a rectangular ring as illustrated in
(40) The electrode surface area of the third electrode 7 should be considerably smaller than the electrode surface area of the first electrode and the electrode surface area of the second electrode in order to ensure that the third electrode allows a free flow of aqueous media from one side to another of the third electrode and to avoid the risk that the third electrode would actively contribute to ion adsorption. If the third electrode has such a large surface area that it actively contributes to ion adsorption, it could risk leading to electrode asymmetry, wherein the ion adsorption of the CDI device will be limited by the capacity of the electrode having the lowest surface adsorption capacity (in this case the third electrode). Preferably, the electrode surface area of the third electrode is maximally 30%, preferably maximally 25%, most preferably maximally 20%, of the electrode surface area of each of the primary electrodes. Moreover, the third electrode preferably has a specific surface area which is less than 5% of the specific surface area of each of the primary electrodes, more preferably less than 2% of the specific surface area of each of the primary electrodes.
(41) Furthermore, in the same manner as in accordance with the prior art disclosed with regard to
(42) As shown in
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(44) As illustrated in
(45) Negatively charged species, in
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(47) The CDI device 20 according to the exemplifying embodiment shown in
(48) The CDI device 20 comprises an outer housing 21 adapted to confine the aqueous media inside the CDI cell during the deionization process. The outer housing 21 has for example a cylindrical configuration such that it comprises a first end surface 21a, an envelope surface 21b, and a second end surface (not shown) opposing the first end surface 21a. The housing comprises an inlet 29 through which the aqueous media is introduced into the CDI device, and an outlet 30 through with the aqueous media exits the CDI device after the deionization. The inlet and outlet may be concentric with the central axis of the CDI device, however other configurations are also possible.
(49) As shown in
(50) As shown in
(51) The power scheme of the CDI device according to the present invention is different from a traditional CDI device since the third electrode is grounded and the primary electrodes polarized with opposite charges with respect to the third electrode. However, in the same manner as a traditional CDI device, the polarization shall be able to be switched such that the CDI device can be regenerated.
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(53) During ion removal or desalination, switch P1 is closed (giving the central electrode of the CDI cell the same potential as the circuit ground), while switches P2 and P3 have their 1 and 3 leads shorted. This configuration leads to current for anionic adsorption (at the positive electrode) to flow from the positive power supply terminal into the CDI cell central electrode (Anion removal current), through the negative electrode into the power supply ground. Similarly the current for the cation adsorption (at the negative electrode) flows from the grounded power supply terminal into the CDI central electrode (Cation removal current), into the CDI negative electrode and back into the power supply negative terminal. Thus the directions of anion and cation charging currents are reversed.
(54) During electrode regeneration, switch P1 is opened (disconnecting the central electrode from the ground potential, while switches P2 and P3 have their 2 and 3 leads shorted. This configuration leads to current for anionic desorption (at the positive electrode) to flow from the positive CDI cell electrode, through switch P2 and into the CDI central electrode in a loop, removing adsorbed anions and giving out energy in the process. Similarly the current for the cation desorption (at the negative electrode) flows from the CDI central electrode, into switch P3 and into the CDI negative electrode in a loop, removing adsorbed cations and giving out energy in the process. Thus the directions of anion and cation desorption currents are the same. The charge stored in the CDI cell electrode will flow as current until all the ions held by the charged electrode surface are removed into the solution.
(55) Thus, as explained above, the two primary electrodes will have equal and opposite potential with respect to the third electrode. However, if the third electrode and the reference terminal from the transformer are left open/floating, then electrically both will develop an active high potential, thus increasing the absolute potential at the two primary electrodes. While the CDI cell in such a case might still function, it will be difficult to determine the absolute reference potential, and it may shift the baseline potential, which can lead to unwanted Faradaic reactions at the two primary electrodes and loss of energy in the process.
(56) A method for manufacturing a capacitive deionisation device preferably comprises the steps of providing a first electrode, arranging a third electrode on a first side of the first electrode and arranging a second electrode on a second side of the third electrode. The third electrode is configured to allow free flow of aqueous media from a first side surface of the third electrode facing the first electrode to a second side surface of the third electrode facing the second electrode. In this method a grounded connection to the third electrode is provided. The first electrode and the second electrode are connected such that they are polarizable with opposite charges with respect to the third electrode.
(57) Further, the method preferably comprises arranging at least one electrically non-conductive spacer between the first electrode and the second electrode. The spacer(s) electrically isolate the electrodes from each other. Preferably fluid is allowed to flow through the spacers with negligible pressure drop. As shown in
(58) Further, the method preferably further comprises arranging the third electrode such that a circumferential outer peripheral edge of the third electrode coincides with a circumferential peripheral edge of the first electrode and/or a circumferential peripheral edge of the second electrode. This helps the third electrode to distribute the electrical field lines appropriately between the electrodes. The third electrode can be arranged as a ring shaped electrode, such as circular ring, a rectangular ring, square ring or octahedral ring, whereby it is ensured inter alia that the third electrode does not cause any physical division of the aqueous media in the device. The third electrode is preferably arranged at substantially equal distances from the first electrode and the second electrode. In this way, symmetric anion and cation removal capacities which prevent unwanted changes in water pH and chemistry are obtained.
(59) According to one variant or embodiment, freely combinable with the other embodiments, the method comprises coating the third electrode on an electrically non-conductive spacer, preferably on a flexible electrically non-conductive spacer. Alternatively, the method comprises embedding the third electrode in a monolithic electrically non-conductive spacer, preferably a flexible monolithic non-conductive spacer. In this embodiment, the method comprises arranging the monolithic electrically non-conductive spacer in direct contact with the first electrode at a first side surface of the monolithic spacer and in direct contact with the second electrode at a second side surface of the monolithic spacer.
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(62) The CDI device according to the present invention can also be achieved by modifying any traditional 2-electrode capacitive deionization unit by introducing the third electrode as described above and adapting the electrical connections such that the third electrode is grounded and the first and second electrode are polarized with opposite charges with respect to the third electrode.
(63) The first and second electrodes are preferably made of flexible electrically conducting material, such as activated carbon cloth having a specific surface area of at least 100 m.sup.2/g, preferably at least 200 m.sup.2/g, more preferably at least 400 m.sup.2/g or 600 m.sup.2/g, more preferably at least 800 m.sup.2/g, and for example preferably a specific surface area of about 1000 m.sup.2/g.
(64) The third electrode may be made of the same material as the first and second electrodes, or made of another material as disclosed above. The electrically non-conductive spacer(s) can be made of any previously known material used for this purpose. The material of the spacer(s) should be an insulating porous material which allows for easy transport of the fluid along with the charged species to be removed. Furthermore, the current collectors can be made of any previously known material for this purpose, for example graphite.
(65) The CDI device according to the present invention may be altered in many ways. For example, the primary electrodes may be made of any kind of material previously known for CDI devices as long as the materials thereof are not specifically provided to obtain an asymmetric ion removal. The primary electrodes are preferably made of the same kind of material. While not necessary, the primary electrodes could also, if desired, be coated with specific, selectively permeable materials to allow only one kind of ion to pass through to each primary electrode, wherein a material allowing only anions can be coated/placed on top/in front of the primary electrode polarized positively with respect to the third electrode and a material allowing only cations can be coated/placed on top/in front of the primary electrode polarized negatively with respect to the third electrode. In this case the first surface of the third electrode would be in contact with the first surface of the material allowing anions through and the second surface of the third electrode would be in contact with the first surface of the material allowing only cations.
(66) Furthermore, the DC power source may be a part of the capacitive deionization device as such. For example, the CDI device may comprise at least one battery, solar cell, fuel cell or the like. Alternatively, the DC power source may be a separate component, in which case the CDI device is configured to be connected to the separate DC power source. For example, the DC power source may be at least one battery, generator or the like. For example, in the case of use of batteries (or solar cells), two batteries can be connected in series, wherein the positive and negative of the first battery and the second battery are shorted and a connection can be extended from this point to the third electrode to act as the reference potential, while the other two battery terminals are connected to the positively and negatively polarized primary electrodes.
(67) While not specifically shown in all of the drawings above, the CDI device preferably also comprises an external housing serving as a protective cover to the other constituent components of the CDI device. The housing is, if so desired, configured to ensure that the aqueous media is confined in the CDI device during the removal of the charged species therefrom. The housing preferably comprises at least one inlet for the aqueous media to enter into the CDI housing. The inlet may, if desired, be further sub-divided into multiple inlet channels to create uniform flow of the fluid within the primary electrodes of the CDI device.
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(69) In case the CDI device is intended to be used for batch use, the inlet also possibly serves as outlet for the aqueous media after the capacitive deionization has been completed to the degree intended or alternatively, there might be an outlet separate from the inlet. However, for most practical applications, the capacitive deionization is intended for a continuous use and hence continuous flow of aqueous media through the device, and the CDI device therefore preferably comprises an outlet for the aqueous media separate from the inlet. Naturally, the CDI device may comprise more than one outlet if desired.
(70) The CDI device according to the present invention is suitable to use in applications where the liquid from which ionic species should be removed is introduced into the CDI device. However, as an alternative, the device is submerged into the liquid from which the ionic species is to be removed. Such a use is exemplified in
(71) In one embodiment, freely combinable with the other aspects and embodiments, the CDI device is a flow-through CDI device wherein the general flow of the aqueous media is essentially parallel to the electrical field between the first electrode and the second electrode. In such a case, the aqueous media passes through at least one of the first electrode and the second electrode, preferably through both the first electrode and the second electrode.
(72) One embodiment is illustrated in
(73) A plurality of such units 120 comprising a perforated pipe and the spiral wound CDI electrodes can be assembled together within a casing or enclosure, forming a cassette 130 as shown in
(74) Such cassettes can be arranged in parallel. This has the advantage of making it possible to adjust the capacity by for example operating one or two cassettes. It also allows the user to regenerate one cassette while the other is active, thus ensuring continuous operation. The use of multiple units, cassettes of assemblies in series or in parallel, as well as in other configurations can be resorted to for increasing the capacity, flexibility, security or the redundance in the system, and they will be obvious to a person skilled in the art.
(75) Alternatively, the CDI device is a flow-by CDI device wherein the general flow of the aqueous media is perpendicular to the electrical field between the first electrode and the second electrode.
(76) The device according to the present invention is preferably used for producing drinking water in power and water scare areas, or producing drinking water in public buildings, hospitals, hotels etc. The device is particularly suitable for remote areas without access to municipal water, areas where the municipal water is of poor or uneven quality, or applications where a high and even quality of the water is desired. The device is also suitable for use in treatment of ballast water on vessels/ships. The device can also be used for the purpose of softening water for private, municipal or industrial applications.
EXPERIMENTAL RESULTS
Example 1. Comparison of the Performance of a Two- and Three-Electrode CDI
(77) The ion removal efficiency of a CDI device comprising two primary ACC electrodes and a central third electrode (hereinafter denominated three-electrode cell) was compared with that of a CDI device comprising only two primary ACC electrodes, i.e. without a central third electrode (hereinafter denominated two-electrode cell). The central third electrode in the three-electrode cell was made of graphite plate.
(78) The primary electrodes for both the two-electrode cell and the three-electrode cell each had an electrode surface area of 9 cm.sup.2. The central electrode, i.e. the third electrode, in the three-electrode cell was in the shape of a ring having a circumferential outer edge following the circumferential outer edges of the primary electrodes and having an electrode surface area of 2 cm.sup.2. The third electrode had a specific surface area equal to 0.5% (1.25 m.sup.2) of the total specific surface area of a single primary electrode (250 m.sup.2). As influent, deionized water with an addition of 1 g/L of NaCl was used and an influent flow rate of 3 mL/min was used.
(79) For the two-electrode cell, the applied DC potential was +1.6 V DC between the two primary electrodes. For the three-electrode cell, the applied DC potential was +0.8V DC between the positive electrode and the central third electrode, and ?0.8V DC between the negative electrode and the central third electrode. Thus, the total potential difference between the primary electrodes of the CDI devices was 1.6 V DC for both the two-electrode cell and the three-electrode cell. Both cells used two layers of cellulose material as the non-conductive spacer, wherein for the three-electrode cell the third electrode was inserted between the two cellulose spacers to electrically isolate it from the two primary electrodes. As the third electrode was in the shape of an open ring and the two primary electrodes were not bound to the rigid current collectors, the distance of the active area (region contributing to ion removal) of the two primary electrodes (open area of the ring) is effectively similar for the two- and three-electrode cells and its effect on ion removal can be neglected.
(80) Conductivity change of the influent was monitored at the output of the cell to measure the ion removal/adsorption efficiency of the CDI devices. Simultaneously, charging and discharging currents were recorded to calculate the power consumption during the desalination process and estimate the total power consumption per m.sup.3 (1000 litres) of water desalted.
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(82) TABLE-US-00001 TABLE 1 Desalination efficiency, salt adsorption capacity and power consumption for two-electrode cell and three-electrode cell, respectively Desalination Specific salt Charge kWh/m.sup.3 efficiency adsorption efficiency of water Configuration (%) (mg/g) (%) desalted two-electrode 22 8.1 68 0.85 cell three-electrode 30 11.3 93 0.61 cell
(83) From the result shown in
(84) The symmetric removal of the ions from the water feed stream also reduces the power consumption for the entire process as illustrated in Table 1. Simultaneously, a 40% improvement in the specific salt adsorption capacity was also evident along with a 37% improvement in the charge efficiency and 28% reduction in kWh/m.sup.3 of desalted water of the three-electrode cell as compared to the two-electrode cell. Charge efficiency basically defines the ratio of charge input in coulombs to the cell to the equivalent coulombic charge of ions removed from the water stream. A charge efficiency of 100% means that for every electron/hole input to the cell, one cation/anion is removed from the cell.
(85) Without further elaboration, it is believed that a person skilled in the art can, using the present description, including the examples, utilize the present invention to its fullest extent. Also, although the invention has been described herein with regard to its preferred embodiments, which constitute the best mode presently known to the inventors, it should be understood that various changes and modifications as would be obvious to one having the ordinary skill in this art may be made without departing from the scope of the invention which is set forth in the claims appended hereto.
(86) Thus, while various aspects and embodiments have been disclosed herein, other aspects and embodiments will be apparent to those skilled in the art. The various aspects and embodiments disclosed herein are for purposes of illustration and are not intended to be limiting, with the true scope and spirit being indicated by the following claims.