INFLATABLE RAZOR
20220024061 · 2022-01-27
Assignee
Inventors
- Efstratios CHRISTOFIDELLIS (Anoixi, GR)
- Nikolaos OVVADIAS (Anoixi, GR)
- Vasileios STAMOULIS (Anoixi, GR)
Cpc classification
B26B21/522
PERFORMING OPERATIONS; TRANSPORTING
B26B21/52
PERFORMING OPERATIONS; TRANSPORTING
International classification
Abstract
This application relates to a handle. The handle may comprise a chamber. The chamber may be inflatable. The handle may be configured to pass from a first state to a second state. The handle may be configured to pass between these states in response to a volumetric change of the chamber. The handle may cooperate with a stand. The handle may be for a handheld device. The handheld device may be a hygiene device. The hygiene device may be a skincare device. The skincare device may be a shaver. The shaver may comprise one or more blades for cutting hair. The shaver may be a razor. The handle and/or the stand may be provided in a kit, a skincare kit, or even a shaving kit.
Claims
1. A handle for a skincare device, the handle comprising an inflatable chamber, the handle being configured to pass from a first state to a second state in response to a volumetric change of the chamber, wherein a volume and/or a girth of the handle in the second state is greater than a volume and/or a girth of the handle in the first state, the handle further comprising a support connected to the chamber wherein the support is arranged on two or more external portions of the chamber.
2. The handle according to claim 1, wherein the chamber includes a first material and the support includes a second material, the second material having a hardness greater than a hardness of the first material.
3. The handle according to claim 1, wherein the support comprises a central body and two or more peripheral bodies, the two or more peripheral bodies being moveable relative to the central body.
4. The handle according to claim 3, wherein the two or more peripheral bodies support a gripping feature.
5. The handle according to claim 3, wherein at least one of the two or more peripheral bodies is formed as a lobe, wherein the lobe has a proximal end connected to the central body.
6. The handle according to claim 3, wherein at least one of the two or more peripheral bodies is formed as a shell separated from the central body.
7. The handle according to any claim 3, wherein at least two or more of the peripheral bodies are connected to one another to form a wrap.
8. The handle according to claim 1, at least a portion of the handle being configured to expand from the first state to the second state in a direction oblique or perpendicular to a longitudinal axis of the handle.
9. The handle according to claim 8, wherein the longitudinal axis is running along a length of the handle and is curvilinear.
10. The handle according to claim 1, comprising a port for changing a volume of the chamber.
11. The handle according to claim 10, wherein the port is removably connectable to a stand.
12. The handle according to claim 10, wherein the port is provided in a bearing surface, wherein the bearing surface facilitates cooperation of the stand and the handle by aiding in proper alignment and connection therebetween.
13. A skincare kit comprising a stand which further comprises a pump, a handle according to claim 1, and a control panel configured to select an on-off condition for the pump.
14. The skincare kit according to claim 13, wherein the stand further comprises a nozzle connected to the pump and being adapted to at least partially inflate and/or at least partially deflate the chamber.
15. A handheld skincare device comprising a handle according to claim 1 and one or more blades for cutting hair.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0048] The disclosure may be more completely understood in consideration of the following detailed description of aspects of the disclosure in connection with the accompanying drawings, in which:
[0049]
[0050]
[0051]
[0052]
[0053]
[0054] While aspects of the disclosure are amenable to various modifications and alternative forms, specifics thereof have been shown by way of example in the drawings and will be described in detail. It should be understood, however, that the intention is not to limit aspects of the disclosure to the particular embodiment(s) described. On the contrary, the intention of this disclosure is to cover all modifications, equivalents, and alternatives falling within the scope of the disclosure.
DETAILED DESCRIPTION
[0055] As used in this disclosure and the appended claims, the singular forms “a”, “an”, and “the” include plural referents unless the content clearly dictates otherwise. As used in this disclosure and the appended claims, the term “or” is generally employed in its sense including “and/or” unless the content clearly dictates otherwise.
[0056] The following detailed description should be read with reference to the drawings. The detailed description and the drawings, which are not necessarily to scale, depict illustrative aspects and are not intended to limit the scope of the disclosure. The illustrative aspects depicted are intended only as exemplary.
[0057]
[0058] The chamber 110 is an inflatable chamber. In such an arrangement, inflation of the chamber 110 causes the volume of the chamber 110 to increase by way of expansion thereof, and/or deflation of the chamber 110 causes the volume of the chamber 110 to decrease by way of contraction thereof. The chamber 110 may be at least partially exposed (e.g. having exterior surfaces).
[0059] The handle 100 may present a central axis 140 running along a length of the handle 100. This axis 140 may be curvilinear, as in the examples shown in
[0060] The chamber 110 is connected to a support 120. The chamber 110 may be arranged between the axis 140 and the support 120. Such an arrangement will be referred to as “exoskeletal”, and will be discussed in greater detail with regard to
[0061] In contrast, if the support 120 is arranged between the axis 140 and an internal surface of the chamber 110, the arrangement will be referred to as “endoskeletal”. A support 120 suitable for an endoskeletal arrangement will be discussed in detail later with regard to
[0062] A handle 100 may include a support 120 that includes both an endoskeletal arrangement and an exoskeletal arrangement. Such an arrangement will be referred to as “hybrid”, and will be discussed in greater detail with regard to
[0063] During changes in girth of the handle 100, at least one element of the support 120 may undergo less deformation than at least one portion of the chamber 110. This may be accomplished, for example, when at least a portion of the chamber 110 is less rigid than at least a portion of the support 120.
[0064] Such a rigidity relationship may be obtained for example, if the chamber 110 includes a first material, and the support 120 includes a second material which is harder than the first material. For example, the chamber 110 may include an elastomeric material. For example, the elastomeric material may include a rubber material, and/or a compressible elastomeric material, such as a thermoplastic rubber, such as, for example, Santoprene™ that was trademarked in 1977 by Monsanto. The support 120 may include a plastic material, for example a moldable non-elastomeric material, such as polypropylene or acrylonitrile butadiene styrene (ABS) resin.
[0065] Hardness of the first and/or second material may be measured using shore durometer type A, for example.
[0066] Non-limiting examples of the geometry of chamber 110 include fixed-length (
[0067] A chamber 110 may be simple (as seen in
[0068] As seen in
[0069] Although not shown in the Figures, other possible arrangements for the support 120 may qualify as exoskeletal. For example, instead of being in contact with an external surface of the chamber 110, the support 120 may provide a section of the chamber 110 itself. In other words, two portions of the chamber 110 may be formed of the second material (i.e. the material of the support 120), and these two portions of the chamber 110 are then linked to each other by way of a portion of the chamber 110 formed of the first material.
[0070] In contrast to an exoskeletal arrangement, an endoskeletal arrangement features a portion of the support 120 which is arranged between an interior surface of the chamber 110 and the central axis 140 of the handle. The support 120 shown in
[0071] Alternatively, the support 120 shown in
[0072] In
[0073] The frame 124 may include one or more holes 125. These holes 125 may reduce weight of the frame 124 and/or material usage to manufacture the frame 124. The holes 125 may alternatively or additionally facilitate movement and/or distribution of fluid within the chamber 110.
[0074] As the handle 100 changes between the low girth state and the high girth state, at least a portion of the handle 100 may move in a direction that is oblique or perpendicular to the longitudinal axis 140. This portion of the handle may be a portion of the support 120, for example.
[0075] Regardless of the type of support 120 (exoskeletal, endoskeletal, or hybrid) used in the handle 100, expansion or contraction of the chamber 110 may cause at least a portion of the support 120 to move in a direction that is oblique or perpendicular to the central axis 140 of the handle 100. Non-limiting examples of the movement of the(se) portion(s) of the support 120 can be seen in
[0076] In
[0077] The examples of
[0078]
[0079] In
[0080] The peripheral bodies 121, 122, 131, 132, 133, 161, 162 may rest on an external surface of the chamber 110. As such, a change in volume of the chamber may cause sliding between the external surface of the chamber and the peripheral body 121, 122, 131, 132, 133, 161, 162. Alternatively, if two peripheral bodies 121, 122, 131, 132, 133, 161, 162 are connected to one another by the first material (i.e. the material of the chamber 110) then a change in volume of the chamber may cause extension and/or retraction of the first material between the peripheral bodies 121, 122, 131, 132, 133, 161, 162.
[0081] At least one of the peripheral bodies 121, 122, 131, 132, 133, 161, 162 may have a concave inner surface disposed towards the central axis 140 of the handle 100. If the peripheral body 121, 122, 131, 132, 133, 161, 162 rests on an external surface of the chamber 110, a concave inner surface may improve stability of the peripheral body 121, 122, 131, 132, 133, 161, 162 on the chamber 110.
[0082] At least one of the peripheral bodies 121, 122, 131, 132, 133, 161, 162 may have a convex outer surface disposed away from the central axis 140 of the handle 100. A convex outer surface may improve comfort when the handle 100 is held in a user's hand.
[0083] In
[0084] To facilitate the movement of the peripheral bodies 131, 132, 133 formed as lobes, at least one lobe may include a flexible region which bends as the lobe(s) deform(s). The flexible region may include a material which is has a lower hardness than an adjoining portion of the lobe. The flexible region may be less rigid than an adjoining portion of the lobe. For example, the flexible region may be thinner in a direction oblique or perpendicular to the axis of rotation of the lobe than an adjoining portion of the lobe.
[0085] A shell differs from a lobe in that a shell is not connected directly to the central body 123, whereas a lobe is connected directly to the central body 123. In
[0086] Additionally or alternatively the path taken by each shell may be defined by the manner in which peripheral bodies 121, 122, 131, 132, 133, 161, 162 are arranged around the central axis 140.
[0087] In
[0088] Alternatively, the peripheral bodies 121, 122 may undergo a linear or curvilinear translation, whereby the taper angle between the peripheral bodies 121, 122 in the low girth state to be substantially equivalent to the taper angle between the peripheral bodies 121, 122 in the high girth state.
[0089] Alternatively, peripheral bodies 121, 122 may undergo a rotation or even a curvilinear translation, whereby the taper angle between the peripheral bodies 121, 122 in the low girth state is higher than in the high girth state.
[0090] The type of movement of the peripheral bodies 121, 122 (i.e. rotation, linear translation, and curvilinear translation) may be determined by the geometry of the chamber 110. For example, a chamber 110 which has a girth that does not vary as a function of position along the central axis 140 may cause a linear translation. For example, a chamber 110 which has a girth that varies as a function of position along the central axis 140, and/or which expands/contracts to varying degrees as a function of position along the central axis 140 may cause a rotation or even a curvilinear translation.
[0091] A shell-type peripheral body 121, 122 as shown in the examples of
[0092] Although such a configuration is not shown in the Figures, a support 120 may include a combination one or more shell-type peripheral bodies (numeric references 121, 122 in the examples of
[0093] In
[0094] A wrap 160 may be connected to the central body 123 by a proximal extremity of the wrap 160. In this case, the peripheral bodies 161, 162 can be considered to be lobes substantially as explained in connection with the examples of
[0095] Alternatively, a wrap 160 may be disconnected from the central body 123, as shown in
[0096] As seen in
[0097] As seen in
[0098] Alternatively/additionally, a gripping feature 170 may be provided on the central body 123, although such an arrangement is not shown in the Figures. The gripping feature 170 may include one or more projections and/or one or more indentations and/or one or more textured regions, and/or one or more layers of material that offer a higher coefficient of friction against human skin than the first material (i.e. the material of chamber 110) and/or the second material (the material of the support 120).
[0099] One example of such a material for the gripping feature 170 may include an elastomer and/or a substance providing good friction when wet. An example of such a substance and/or of an elastomer may be a rubber. In
[0100] Although
[0101] As seen in
[0102] Although such a configuration is not visible in the Figures, the port 150 may be arranged in other areas of the handle 100. For example, the port 150 may be arranged in the central body 123 of the support 120, or in a peripheral body 121, 122, 131, 132, 133, 161, 162 of the support 120, or even may be arranged in an exposed exterior surface of the chamber 110. Any of these arrangements would be suitable for use with the support 120 shown in
[0103] Although not shown in the Figures, the handle 100 may include a button. The button may be connected to a valve, such that operation of the button (such as by pressing, contacting, releasing, etc.) leads to a change of state of the valve. For example, operation of the button may allow a user to open and/or close the valve, and/or assume a partially-open (partially-closed) position. At least a part of the valve may be located within the chamber 110. Additionally or alternatively, at least a part of the valve may be located outside of the chamber 110. As a non-limiting example, the button may allow a user open and/or close and/or partially open (partially close) the port 150, so that fluid may pass therethrough.
[0104] As seen in
[0105] To that end, the port 150 may be provided in a bearing surface 126, as seen in
[0106] Although
[0107] As mentioned earlier herein, the support 120 shown in
[0108] Independently of whether the handle 100 features an endoskeletal arrangement, an exoskeletal arrangement, or a hybrid arrangement, a branched chamber 110 may be provided such that each branch 110 corresponds to a peripheral body 121, 122, 131, 132, 133, 161, 162. For example, in
[0109] The pump 200 may allow fluid to be delivered to the handle 100 and/or extracted from the handle 100. If a port 150 is present in the handle 100, fluid delivered by the pump 200 may be introduced into the chamber 110 by way of the port 150, and/or fluid extracted by the pump 200 may be removed from the chamber 110 by way of the port 150. Extraction of fluid by pump 200 may be possible without regard for whether passive exhaustion of fluid from the chamber 110 is possible.
[0110] The stand 220 may include a nozzle 210 connected to a pump to facilitate delivery fluid to the handle 100 and/or extraction fluid from the handle 100. The nozzle 210 may be connectable, disconnectable, or even removably connectable to the handle 100. If a port 150 is present in the handle 100, the nozzle 210 may cooperate with the port 150. In this way, fluid delivered to the handle 100 and/or extracted from the handle 100 by the pump 200 through the nozzle 210 may be introduced into the chamber 110 and/or removed from the chamber 110 by way of the port 150. Non-limiting examples of cooperation between the nozzle 210 and the port 150 include connectability, disconnectability and removable connectability. Cooperation between the nozzle 210 and the port 150 may be penetrative or non-penetrative.
[0111] As seen in
[0112] The stand 220 and the handle 100 may each be provided with corresponding surfaces that cooperate to curtail inadvertent disconnection of the port 150 and the nozzle 210 during introduction of fluid into the chamber 110 and/or removal of fluid from the chamber 110.
[0113] Moreover, as can be seen in
[0114] The handle 100 may be suitable for a device. The device may include an attachment and the handle 100. The device may be a handheld device. The handheld device may be a skincare device 300 as seen in
[0115] The adjustable girth of the handle 100 may improve ergonomics of use of the device, and/or may facilitate safe and/or comfortable manipulation of the handle 100 and maneuvering of any attachment borne thereon.
[0116] In the context of a skincare device 300, the improvements in ergonomics may allow a user to care for skin in a manner that is more comfortable and/or safer and/or more effective than may be possible for a handle that is ergonomically maladapted to the user's hand.
[0117] Moreover, and independently of the context of skincare, the adjustable girth of the handle 100 may allow the benefits of the handle 100 to be conferred to multiple hands of different sizes (as can happen if the handle is shared between users) with a single handle 100. This provides for a more versatile skin care device, as the same handle may fit different hand sizes, thus allowing the same handle to be marketed to a wider range of potential users than a single handle of fixed girth.
[0118] In the handle 100 as described earlier herein, the central body 123 provides an attaching location for a device's attachments. Thus, in the skincare devices 300 shown in
[0119] When the handle 100 is connected to the attachment directly, the handle may include a coupling mechanism for connecting to the attachment. Coupling mechanism are also well known and may be found e.g. WO2015158382, which is incorporated herein in its entirety, including from page 6, line 23 to page 26, line 2 (notably lines 23-25 of page 6, from line 35 of page 6 to line 8 of page 8, from line 9 of page 11 to line 3 of page 12, and from line 10 of page 13 to line 2 of page 26) as well as
[0120] Forces applied by the user to an exterior surface of the handle 100 may be transmitted to the central body 123 of the support 120. If an attachment is connected to the handle 100, the central body 123 may transmit forces from the handle 100 to the attachment. As such, a user may be able to maneuver the attachment by manipulating the handle 100.
[0121] In the skincare device 300 shown in
[0122] The stand 220 and/or the handle 100 and/or a device including the handle may form part of a kit. The kit may include a control panel. The control panel may be configured to select an operating parameter for the pump 200. This operating parameter may include an on-off condition for the pump 200. The on-off condition may include or be a shutoff condition for the pump 200. Non-limiting examples of operating parameters for the pump include fluid flow rate and/or fluid pressure and/or fluid quantity. For example, the pump 200 may be configured to modify the pressure and/or volume of the chamber 110 by delivering or extracting fluid until the fluid within the chamber 110 reaches a certain pressure and/or until the chamber 110 contains a certain volume of fluid, and/or until the pump 200 has introduced/removed a certain volume of fluid from the handle 100.
[0123] The control panel may be provided on the stand 220 (if present in the kit) and/or on the handle 100 (if present in the kit) and/or on a device including the handle 100 (if present in the kit). Additionally or alternatively, the control panel may be provided on an additional device, for example in the form of a software user interface. Additionally, having such a versatile handle forming part of a kit provides for multiple interrelated actions to be taken using the same handle, e.g. exfoliation or shaving can be done using the same handle if the shaving cartridge is replaced with an exfoliation head. This provides for adaptability of the handle in between these two actions, e.g. if for one of the actions the user prefers a smaller/bigger handle girth size than for the other. Alternatively, it allows for different users, e.g. male/female, to have their own cartridge and share the same handle.
[0124] The control panel may be configured to prevent excessive introduction of fluid into the chamber 110 and/or excessive removal of fluid from the chamber 110. As a non-limiting example, the control panel may accomplish this function based on readings of a sensor configured to measure the fluid. As a non-limiting example, the control panel may drive the pump 200 until the sensor indicates that additional fluid introduction or removal would become excessive. At this point, for example, the control panel may stop driving the pump 200. For example, excessive fluid introduction or removal may lead to the handle 100 having a girth that is different than is desired by a user. For example, excessive removal of fluid may cause the handle 100 to have a girth that is less than is desired by the user. For example, excessive introduction of fluid may cause the handle 100 to have a girth that is greater than is desired by the user. To prevent such problems, the sensor may be configured to measure volumetric flow. A user may be able to specify a pressure of fluid in the chamber 110 and/or a volume of fluid introduced into/removed from/contained in the chamber 110, and/or a girth of the handle 100.
[0125] Excessive fluid introduction or removal may also cause damage to the handle 100 (for example a burst chamber 110) and/or pump 200 (for example a worn out pump 200), and/or disconnection of the pump 200 and the handle 100 when such disconnection is not desired or performed by a user, and/or difficulty for a user to disconnect the pump 200 from the handle 100 when such disconnection is desired. To avoid such problems, the sensor may include a pressure sensor.
[0126] The control panel may be configured to prevent a user from selecting a pressure and/or volume of the chamber 110 and/or a girth of the handle 100 that would necessitate the pump 200 running until one or more of these scenarios was generated.
[0127] As non-limiting examples, returning to
[0128] The presence of at least one opening in the chamber 110 (such as may be provided by a port 150) may allow fluid to move into or out of the chamber 110 as needed to change the girth of the handle 100. However, to maintain a given girth, it may be desirable to prevent this movement (at least intermittently). To that end, the opening may be sealed.
[0129] A port 150 may contribute to sealing such an opening, or may even be entirely responsible for sealing the opening.
[0130] All variants of the support 120 described herein may be compatible with use of a port 150, and this port 150 may even be used to seal an opening in the chamber 110 of the handle 100 in which the support 120 is provided.
[0131] Additionally or alternatively, an opening in the chamber 110 may be sealed using other techniques. For example, an opening in the chamber 110 may be sealed by fixing the opening to another component of the handle 100. Non-limiting techniques for fixing a chamber 110 to another component of a handle 100 include (but are not limited to) gluing the chamber 110 to the component, and/or over-molding the chamber 110 on the component (or over-molding the component on the chamber), and/or injection molding and/or blow molding of the chamber 110 and/or of the component.
[0132] Non-limiting examples of components of the handle 100 which are suitable for sealing of an opening in the chamber 110 by fixation of the chamber 110 thereto can be seen in the figures.
[0133] According to aspects, the foot 127 may contribute to sealing an opening in the chamber 110. For example, in
[0134] The foot 127 may be monolithic, as shown in
[0135] The foot 127 may contribute to sealing an opening of the chamber 110 on its own, or the foot 127 may cooperate with another element of the handle 110, such as the support 120, to contribute to sealing an opening in the chamber 110. For example, in
[0136] The support 120 may also contribute to sealing an opening of the chamber 110 on its own (i.e. without cooperating with another element of the handle 110). For example, in
[0137] Likewise, the central body 123 of the support 120 may contribute to sealing an opening in the chamber 110 on its own (i.e. without cooperating with another element of the support 120 or the handle 110). For example, instead of being sandwiched between the central body 123 and the frame 124, the chamber 110 may simply be sealed against a portion of the central body 123 using any suitable technique, including those presented earlier herein. This portion of the central body 123 may be an interior surface of the central body 123. On the other hand, in
[0138] A peripheral body 121, 122, 131, 132, 133, 161, 162 may also contribute to sealing an opening in a chamber 110. For example, the opening may be fixed around a peripheral body. For example, a lobe 131, 132, 133 may be inserted into an opening in the chamber 110 and the opening fixed therearound using any suitable technique, including those presented earlier herein, to seal the opening. A similar technique may be used for a wrap-type peripheral body 161, 162 or a shell-type peripheral body 121, 122.
[0139] When a port 150 is provided for any of these openings, the port 150 may be provided independently of the chamber 110, and arranged in a hole provided in the component of the handle 100 against which the opening is sealed. Non-limiting examples of such holes can be seen in the foot 127 of
[0140] Alternatively, a port 150 may seal an opening in the chamber 110 on its own (i.e. without cooperating with other elements of the handle 100). For example, the port 150 may be provided in the chamber 110 itself. In such a configuration, the chamber 110 may be arranged in the handle 100 such that the port 150 is arranged in a hole provided in one of the other components of the handle 100. Although such holes may be seen in the foot 127 of
[0141] Although sealing an opening in the chamber 110 with another component of the handle 100 may have the effect of fixing the chamber 110 thereto, it is also possible to fix the chamber 110 to another component of the handle 100 without sealing an opening in the chamber 110. In other words, all of the techniques described herein for sealing an opening in the chamber 110 to another component of the handle 100 may also be suitable for simply fixing the chamber 110 to the component of the handle 100.
[0142] For example, in
[0143] The measures taken to seal an opening in the chamber 110 may also allow for local stabilization of the chamber 110 within the handle 100. As such, a tube-like chamber 110, or a tube-like branch of a chamber 110 may be stabilized at multiple locations simply by being sealed. In contrast, with a balloon-like chamber 110, or a balloon-like branch of a chamber 110, it may be desirable to provide additional fixation beyond that which may be provided simply by sealing. For example, the chamber 110 of the handle 100 shown in
[0144] Additionally or alternatively, any of these techniques may be used to fix the chamber 110 to one or more of the peripheral bodies 121, 122 of the support 120, independently of whether the chamber 110 presents an opening to be sealed at the site of fixation. Moreover, any of these techniques may also be suitable for fixing the chamber 110 to one or more of the peripheral bodies of a support 120 having one or more lobe-type peripheral bodies 131, 132, 133 and/or one or more wrap-type peripheral bodies 161, 162.
[0145] The chamber 110 may be fixed and/or sealed one or more on surfaces of the support 120 which are arranged to face the chamber 110. As non-limiting examples, these surfaces may be provided by the central body 123, by a peripheral body, 121, 122, 131, 132, 133, 161, 162, or other elements of the handle 100. Alternatively or additionally, chamber 110 may even be fixed and/or sealed on one or more edges of the support 120, such as the peripheral edge of a peripheral body 121, 122, 161, 162.
[0146] For example, in
[0147] Similarly, in
[0148] The foregoing discussion relating to fixation of a chamber 110 and/or sealing of an opening in a chamber 110 is applicable whether the chamber 110 is simple or branched. In the case of a branched chamber 110, the foregoing discussion may apply to each branch of the chamber 110 individually or even to a portion of the chamber 110 connected to multiple branches thereof.
[0149] Although the described embodiments were provided as different exemplary embodiments, it is envisioned that these embodiments are combinable or, when not conflicting, the features recited in the described embodiments may be interchangeable. Moreover, the features recited in the described embodiments are not inextricably linked to one another, unless such a linkage is clearly indicated between two given features.
[0150] Throughout the description, including the claims, the term “comprising a” should be understood as being synonymous with “comprising at least one” unless otherwise stated. The same applies for “including a” with regard to “including at least one”. In addition, any range set forth in the description, including the claims should be understood as including its end value(s) unless otherwise stated. Specific values for described elements should be understood to be within accepted manufacturing or industry tolerances known to one of skill in the art, and any use of the terms “substantially” and/or “approximately” and/or “generally” should be understood to mean falling within such accepted tolerances.
[0151] Although the present disclosure herein has been described with reference to particular embodiments, it is to be understood that these embodiments are merely illustrative of the principles and applications of the present disclosure.
[0152] It is intended that the specification and examples be considered as exemplary only, with a true scope of the disclosure being indicated by the following claims.