This disclosure relates generally to containers for fluids. More particularly, this disclosure relates to containers for dispensing fluid.
Product separation is an issue that arises with many fluid products that have two or more fluid types in a mixture. Product separation often results as the fluid product settles over time with a lower density fluid separating from a higher density fluid of the fluid product. For instance, a thin or relatively low viscosity, low density fluid may separate from the remainder of a fluid and rest on top of the remainder of the fluid. One example of such a fluid where product separation is prone to occur is ketchup. Over time, serum or water separates from the remainder of the ketchup fluid, with the serum or water rising to the top of the fluid mixture. Product separation is undesirable in many applications and particularly in applications where the fluid product is dispensed directly from a container where the user may not be aware that product separation has occurred. As a result of product separation, when a user dispenses the fluid from the fluid container, the low viscosity, low density fluid may be dispensed separately from the remainder of the product rather than as a mixed fluid product. Dispensing the lower viscosity fluid may result in increased splatter as the user dispenses the fluid from the fluid container. Moreover, the thin or lower viscosity fluids may more readily leak from the fluid container.
Some have attempted to address these problems by using a dispensing cap with a bottle that facilitates mixing of the fluid within the bottle as the fluid is dispensed. These dispensing caps, however, are often large in size, having intricate internal pieces and mixing channels within the closure cap. Such dispensing caps are generally expensive to manufacture and are overly large which makes them difficult to ship and store (e.g., take up too much shelf space in the store and/or at home).
Described herein are systems, apparatus and methods for dispensing a fluid from a bottle, such as, consumer or food products including, e.g., condiments or drinks. In some embodiments, a bottle includes a fitment that is configured to facilitate dispensing of fully mixed product and prevent discharge of separated constituents, such as, e.g., watery serum. In some configurations, the dispensing bottle includes a serum well that captures or retains at least some of the separated serum, thereby preventing it from discharging from bottle, at least until this separated serum has been sufficiently mixed into a remainder of the fluid. While some previous solutions required complicated or large closure caps, others suffered from a decrease in functionality. For example, certain closure caps that prevented the discharge of separated serum, also required a very large internal pressure to eject the fluid therefrom, thereby requiring the consumer to apply a larger force to the outside of the dispensing bottle.
Various dispensing bottles 10 are provided herein that facilitate mixing of the constituent parts of a fluid contained therein prior to discharge from the dispensing bottle 10 and/or prevent separated fluid from being dispensed from a container body 12 of the dispensing bottle 10. In some illustrative embodiments, the dispensing bottle 10 includes a serum trap or serum well 44 for the separated fluid (e.g., serum) to flow into where the separated fluid is not able to flow directly out of the dispensing bottle 10 and be dispensed to the user without being mixed with a remainder of the fluid. For example, where serum or water has separated from the fluid (e.g., ketchup) within the dispensing bottle 10, as the dispensing bottle 10 is inverted, the serum or water flows into the serum well 44. The serum well 44 is formed by a tube 38 of a fitment 34 that extends into the container body 12 and serves as a snorkel that fluid from further into the container body 12 enters to be dispensed to the user. For example, where serum or water has separated from the fluid (e.g., ketchup), as the dispensing bottle 10 is inverted, the serum or water flows or is retained within into the serum well 44 and below the inlet opening 41 of the tube 38 of the fitment 34. The mixed or non-separated fluid flows on top of the serum within the serum well, trapping the separated fluid within the serum well and preventing the separated fluid from flowing into the inlet opening 41 of the tube 38 and along a fluid flow channel 42 of the tube 38 out of the container body 12. The mixed or non-separated fluid outside of the serum well 44 and above the inlet opening 41 of the tube 38 of the fitment, however, is able to flow into the fluid flow channel 42 of the tube 38 and out of the dispensing bottle 10.
In some configurations, by having the tube 38 of the fitment 34 extend into the neck of the container body 12, the dispensing bottle 10 may include a closure cap 18 with a relatively low profile while preventing separated fluid from being dispensed from the dispensing bottle 10. More particularly, the location of the tube 38 provides a serum well 44 at least partially disposed in the neck 14 of the container body 12. Thus, the closure cap of the dispensing bottle 10 may have a smaller size that is more easily shipped and/or stored. The dispensing bottle 10 also may be economically manufactured as it lacks intricate internal components that require specialized manufacture.
In addition, the dispensing bottle 10 also may include a closure cap 18 that prevents unintentional discharge of fluid therethrough. The dispensing bottle 10 may be stored while resting on the closure cap 18 or on the base of the container body 12. Therefore, the closure cap 18 typically includes structure to both sufficiently retain the fluid in the bottle 10 when the closure cap 18 is in a closed configuration and the container body 12 is disposed above or below the closure cap 18.
With respect to
In some embodiments, the closure cap 18 includes a base 26 and a flip-top lid 28 hingedly connected to the base 26 via hinge 30. The flip-top lid 28 may be moved between open (not shown) and closed positions about the hinge 30. The base 26 of the closure cap 18 includes a central member 20 with a dispensing opening 32 therein for fluid to flow through the closure cap 18 to dispense the fluid within the container body 12. The closure cap 18 may be attached to the neck 14 of the container body 12 and the flip-top lid 28 moved between open and closed positions to selectively permit the fluid to exit the container body 12. The flip-top lid 28 may prevent fluid from exiting the dispensing opening 32 when the flip-top lid 28 is closed and may permit fluid from exiting the dispensing opening 32 when the flip-top lid 28 is open. The flip-top lid 28 may include a projection 29 that closes or plugs the opening 32 when the flip-top lid 28 is in the closed position. The projection 29 may be at least partially inserted into the opening 32 to plug the opening 32. The projection 29 may be removed from the opening 32 when the flip-top lid 28 is moved toward the open position to thereby permit fluid to exit the opening 32.
The base 26 of the closure cap 18 includes an inner skirt 22 depending from the central member 20. The base 26 may further include an outer skirt 23 depending from the central member 20. The inner skirt 22 and the outer skirt 23 may be substantially concentric with the opening 32 of the base 26. The inner skirt 22 has skirt threads 24 disposed on an inner surface thereof that correspond to the neck threads 16 of the container body 12. The closure cap 18 may be secured to the container body 12 by threading the skirt threads 24 of the base 26 to the neck threads 16 of the neck 14 of the container body 12. The outer skirt 23 may depend from an outer edge of the central member 20. The outer skirt 23 may form a shell about the inner skirt 22 and the neck 14 of the container body 12. The closure cap 18 may be formed of a plastic material, such as, polypropelene, polyethylene (e.g., HDPE, LDPE, LLDPE, MDPE, HMWPE), PET, or other food grade plastic or polymer.
With reference also to
In some configurations, the tube 38 extends from the base portion 36 about the central opening 40 to an inlet opening 41. When the fitment 34 is secured to the container body 12, at least a portion of the tube 38 of the fitment 34 extends into the container body 12 (e.g., into the neck 14) such that the inlet opening 41 of the tube 38 is within the container body 12, disposed a distance from an opening defined by the upper surface or rim of the neck 14. In use, the tube 38 typically forms a fluid flow channel 42 within a portion of the neck 14 of the container body 12 from the inlet opening 41 to the opening 40 of the base portion 36 of the fitment 34. By positioning the inlet opening 41 within the neck 14 of the container body 12, the inlet opening 41 of the tube 38 receives fluid from further into the container body 12 rather than the fluid adjacent the base portion 36 of the fitment 34. The fitment 34 thereby forms the serum well 44 within the neck 14 of the container body 12 with the tube 38 serving as a snorkel for dispensing fluid from further inside the container body 12.
The serum well 44 typically includes the volume of fluid within the dispensing bottle 10 disposed radially outward of the tube 38 that is not able to flow into the fluid flow channel 42 through the inlet opening 41. For instance, when the dispensing bottle 10 is inverted to dispense the fluid (or is resting stably on its closure cap), the separated fluid (e.g., serum, water) flows to or pools at the base portion 36 of the fitment 34. The separated fluid is thus radially outward of the tube 38 of the fitment 34 or outside the fluid flow channel 42 and, where the volume of the serum well 44 is greater than the volume of the separated fluid, the separated fluid is disposed below the inlet opening 41 of the tube 38 of the fitment (when the dispensing bottle 10 is inverted) and is not able to enter the fluid flow channel 42 through the inlet opening 41. The size of the serum well 44 may be adjusted by adjusting the length and diameter of the tube 38. As examples, the tube 38 may have a length in the range of about 6 mm to about 25 mm. In one specific example the tube 38 may have a length of 10 mm. As another specific example the tube 38 may have a length of 14 mm. The serum well 44 may have a volume in the range of about 2 mL to about 15 mL, and in one specific example 5 mL. As another specific example, the serum well 44 may have a volume of 6.4 mL. The fitment 38 may be formed of a plastic material, such as, polyethylene, polypropylene, polyethylene terephthalate. In addition, the outside diameter of the tube 38 may be, for example, 6 mm.
In one illustrative approach, when the closure cap 18 is secured or threaded onto the container body 12, the upper surface of the base portion 36 of the fitment 34 abuts an interior surface of the central member 20 such that the tube 38 forms a fluid flow channel 42 to the opening 32 of the central member 20 of the closure cap 18. The tube 38 and the opening 40 in the base portion 36 may be aligned with the opening 32 of the central member 20 of the closure cap 18 when the closure cap 18 is secured to the container body 12. The base portion 36 of the fitment 34 may form a sealed connection with the closure cap 18 when the closure cap 18 is secured to the container body 12 such that fluid is only able to flow from the fitment 34 and through the dispensing opening 32 of the central member 20 and is not able to flow between the base portion 36 of the fitment 34 and the central member 20 of the closure cap 18. In one form, the central member 20 of the closure cap 18 includes an annular seal ring about the opening 32 that engages the upper surface of the base portion 36 about the opening 40 in the base portion 36.
In some configurations, the base portion 36 of the fitment 34 may further include one or more access openings 46 radially outward of the central opening 40. In the embodiment of
In some embodiments, the base portion 36 of the fitment 34 also forms a fluid tight seal with the closure cap 18 when the closure cap 18 is secured to the container body 12 to prevent fluid from flowing out of the container body 12 through the access openings 46. For example, portion(s) of the fitment 34 may abut the central member 20 and form a sealed connection therebetween to prevent fluid from unintentionally flowing between the base portion 36 of the fitment 34 and the central member 20 of the closure cap 18. In one form, the closure cap may include seals that are configured to contact the upper surface of the base portion 36 of the fitment 34 about the access openings 46 to prevent fluid from exiting the container body 12 via the access openings 46. In other embodiments, the fitment 34 does not include access openings 46 and is similar to the fitment 334 shown in
In one exemplary approach, the distal end of the tube 38 of the fitment 34 opposite the base portion 36 may include a diverter cone 50 supported by arms 52 above the inlet opening 41 of the distal end of the tube 38 into the fluid flow channel 42. The diverter cone 50 may aid to prevent separated fluid from falling or flowing into the tube 38 as the dispensing bottle 12 is inverted. For instance, when the dispensing bottle 10 is resting with the neck 14 facing upward, serum or separated fluid may gather on the top surface of the fluid within the container body 12. As the dispensing bottle 10 is inverted, for example, to dispense the fluid, the serum or separated fluid may fall or flow toward the fitment 34 and neck 14 of the container body 12 toward the serum well 44. The diverter cone 50 redirects the fluid toward the serum well 44 and around the tube 38 as the serum passes over the diverter cone 50 and aids to prevent the serum from entering the inlet opening 41 of the tube 38 and being dispensed. The non-separated fluid will flow on top of the serum and trap the serum within the serum well 44. The non-separated fluid will then flow between the diverter cone 50 and the tube 38 and into the inlet opening 41 of the tube 38 through two opposing openings between the arms 52 to dispense the fluid to the user.
In some configurations, the dispensing bottle 10 includes a liner 48 that may be sealed to the rim of the neck 14 of the container body 12 and/or the base portion 36 of the fitment 34. In the embodiment of
To dispense fluid from the dispensing bottle 10, the dispensing bottle 10 may be inverted or turned so that the closure cap 18 and the neck 14 of the container body 12 are facing downward below a remainder of the container body 12. As the dispensing bottle 10 is inverted, the separated fluid or serum typically flow toward the base portion 36 of the fitment 34 and into the serum well 44 radially outward of the tube 38 of the fitment 34. The diverter cone 50 typically directs the separated fluid or serum away from the inlet opening 41 of the tube 38 and toward the serum well 44. The non-separated fluid may flow on top of the separated fluid or serum within the serum well 44 thereby trapping the serum and preventing the serum from exiting the container body 12 via the tube 38. Whether before or after the closure cap 18 is placed below the container body 12, the flip-top lid 28 may be opened to remove the projection 29 from the opening 32 in the central member 32 and to thereby permit fluid to exit the container body 12 through the opening 32 in the central member 32 along the fluid flow channel 42. A user may squeeze the container body 12 to force fluid to flow from the container body 12, under the diverter cone 50, into the tube 38 via inlet opening 41, along the fluid flow channel 42, and out the dispensing opening 32.
With respect to
With respect to
The dispensing bottle may include a closure cap 118 that further includes a fitment 134. The fitment 134 includes a base portion 136 including a central opening 140 and one or more access openings 146 radially outward of the central opening 140. The fitment 134 includes a tube 138 extending from the base portion 136 about the central opening 140 such that the tube 138 forms a fluid flow channel 142 within the tube 138 toward the central opening 140 of the base portion 136 of the fitment 134 and a dispensing opening 132 of the closure cap 118 when the closure cap 118 is secured to the container body 112.
With this second embodiment, the base portion 136 of the fitment 134 includes one or more attachment extensions 160 (e.g., one annular extension) about the periphery of the base portion 136 for attaching to a portion of the container body, such as, e.g., the neck 114 of the container body 112. In some forms, the attachment extension 160 aid in aligning the fitment 134 with the neck 114 of the container body 112 and preventing the fitment 134 from moving substantially such that the fitment 134 may be welded to the container body 112. In some forms, the base portion 136 of the fitment 134 may attach to the neck 114 of the container body 112 in a variety of manners, such as, by a snap-fit or friction-fit connection, among others. As shown in
In other forms, the attachment extension(s) 160 may engage or be secured to an inner surface of the neck 114 of the container body 112. In illustrative one form, the attachment extension 160 includes an annular or partially annular attachment wall (or walls) that depend from the base portion 136 of the fitment 134. The attachment wall may include a deflectable angled tip or barb that snaps over a ridge or into a groove that extends about the outer or inner surface of the neck 114 of the container body 112.
In some configurations, the liner 148 may be secured to the upper surface of the base portion 136 of the fitment 134 to seal the contents of the container body 112. Where the attachment extensions 160 attach to the inner surface of the neck 114 of the container body 112, the liner 148 may be attached to the base portion 136 of the fitment 134 and/or the neck 114 of the container body 112. In some forms, the dispensing bottle 10 may further include a second seal (similar to the seal 54 described above) positioned between the base portion 136 of the fitment 134 and the neck 114 of the container body 112.
With respect to
The fitment 234 of the dispensing bottle includes a base portion 236 and a tube 238 extending from the base portion 236 as in the previous embodiments. The fitment 234 is configured to be inserted into the neck 214 of the container body 212 and be held in place by a friction-fit engagement, snap-fit engagement, and/or other connection mechanisms with the interior of the neck 214 of the container body 212. As shown in
In some approaches, the fitment 234 includes guiding fins 235 depending from the base portion 236 of the fitment 234 that aid in aligning the fitment 234 with the neck 214 of the container body 212. At least a portion of the guiding fins 235 may slide beyond the step 214A of the neck 214 to ensure the fitment 234 is properly oriented and aligned with the neck 214 as the fitment 234 is inserted into the neck 214. The increased axial engagement of the guiding fins 235 with the neck 14 may further aid in preventing the fitment 234 from rotating or pivoting relative to the container body 212 once inserted into the neck 214. The guiding fins 235 may further increase the frictional engagement between the fitment 234 and the container body 212 to aid in preventing the fitment 234 from inadvertently being withdrawn for forced out of the container body 212 once inserted therein.
As shown in
In some forms, the inner surface of the neck 214 of the container body 212 includes an annular or partially annular groove that receives the radial outer edge of the base portion 236 of the fitment 234. The fitment 234 may be inserted into the neck 214 of the container body 212 until a peripheral edge of the base portion 236 of the fitment 234 snaps into the groove of the neck 214 to secure the fitment 234 to the container body 214 by a snap-fit connection.
With respect to
The fitment 334 may be similar to the fitments of the previous embodiments including a base portion 336 and a tube 338. The base portion 336 of the fitment 334 may be configured to be attached to the neck 314 of the container body 312 as described with respect to any of the previous embodiments. The fitment 334 may include a central opening 340 from which a tube 338 may extend to form a fluid flow channel 342 through which the fluid may be dispensed from the container body 312. In the embodiment shown, the base portion 336 of the fitment 334 does not include access openings as in the prior embodiments. This ensures that fluid only exits the container body 312 through the central opening 340 of the fitment 334. The fitment 334 may be removeable from the container body 312 (e.g., by unsnapping or forcing the fitment from the container body) to allow a user to fully empty the container body 312 and/or to rinse the container body 312.
With respect to
The fitment 434 may be attached to the closure cap 18 by a snap-fit and/or friction fit connection, among other options. In some configurations, the closure cap 418 includes a groove 456 (
In some forms, the base portion 436 of the fitment 434 may additionally or alternatively be secured to the closure cap 18 by an adhesive. For example, an adhesive may secure the upper surface of the base portion 436 of the fitment 434 to the central member 420 of the closure cap 18. In some forms, the closure cap 18 does not include a groove 456 or ridge 448. Additionally or alternatively, the fitment 434 may be held within the inner skirt 422 of the closure cap 418 by frictional engagement of the peripheral edge of the base portion 436 of the fitment 434 with the inner surface of the inner skirt 422. In other forms, the fitment 434 is formed integrally or as a unitary piece with the closure cap 18. For instance, the fitment 434 is molded as a single piece with the closure cap 18. For example, the closure cap 18 may include a tube (similar to tube 438 of the fitment 434) depending from the central member 420 of the closure cap 18 about the dispensing opening 432.
The dispensing bottle 410 also differs from prior embodiments in that the dispensing bottle 410 typically does not include a liner between the fitment 434 and the closure cap 418. The closure cap 418 may form a sealed connection with the container body 12 using other approaches that do not require a seal liner over the opening of the fitment 434. For example, the dispensing opening 432 of the closure cap 418 may include a removeable seal that seals the opening before use. The closure cap 418 may form also form a sealed connection with the container body 412 when attached thereto (e.g., between the inner skirt 422 and the neck 414 of the container body 412). In other configurations, a seal may be disposed below the closure cap and the fitment at the neck of a bottle.
In each of the above embodiments, the length and diameter of the tube 38 of the fitment 34 may be adjusted based on the type of fluid to be dispensed from the dispensing bottle 10. For example, for higher viscosity fluids, a larger diameter tube 38 may be used. As another example, for fluids that are prone to separation a longer tube 38 may be used to create a greater volume serum well 44 such that fluid from further within the container body 12 is dispensed. Thus, the size of the fitment 34 may be selected based on the type of fluid that will be within the dispensing bottle 10. For example, a fitment 34 may be used that has a tube 38 that is optimized for a particular fluid type based on the fluid properties and separation characteristics of the fluid. The closure cap 18 may be compatible with several fitments 34 having different sized tubes 38 such that the closure cap 18 may be used for fluids of all types with the type of fitment 34 being selected and used based on the type of fluid to be dispensed from the container body 12. For example, the same container body 12 and closure cap 18 may be used for dispensing several different condiments (e.g., ketchup, barbeque, mustard, etc.) with the fitment 34 (e.g., the size of the tube 38 of the fitment 34) varying based on the condiment within the container body 12. With respect to the dispensing bottle 410 of
The dispensing bottle 10 may be manufactured according to the following processes. While the following discussion primarily makes reference to the dispensing bottle 10 of the first embodiment, those having skill in the art will readily appreciate that these steps may also apply to the dispensing bottles of the other embodiments. The container body 12 may be molded as a receptacle having an interior volume for receiving and storing fluid therein. The container body 12 may be molded to include a neck 14 with threads thereon for securing the container body 12 to the closure cap 18. The container body 12 may be filled with a fluid product such as a thixotropic fluid through to opening in the neck 14 of the container body 12. The closure cap 18 may be molded to form a cap including base 26 having a central member 20 with a skirt 22 depending from the central member 20. The skirt 22 includes threads 24 thereon that correspond to the neck threads 16 to enable the closure cap 18 to be secured to the neck 14 of the container body 12. In some forms, the central member 20 of the closure cap 18 may form a portion of the base 26 to which the flip-top lid 28 is hingedly connected to via hinge 30. The central member 20 may also be formed with a dispensing opening 32 therein.
A seal liner 48 may be positioned within a recess 72 of the closure cap 18 formed by the central member 20 and the skirt 22 as shown by arrow 74 of
The closure cap 18 may be attached to the neck 14 of the container body 12 with the liner 48 and the fitment 34 within the recess 72 of the closure cap 18. As the closure cap 18 is attached to the container body 12, the tube 38 of the fitment 34 may be aligned with and inserted into the opening of the container body 12 formed by the neck 12. The liner 48 may be sealed to at least one of the neck 14 of the container body 12 and/or the fitment 34. As one example, the dispensing bottle 10 may undergo induction sealing to seal the liner 48 to the fitment 34. In embodiments where the second seal 54 is used, the second seal 54 may be sealed to the neck 14 of the container body 12 and the base portion 36 of the fitment 34. In some forms, the liner 48 and the second seal 54 are sealed simultaneously by an induction sealing process.
In forms where the second seal 54 is not used, the induction sealing of the liner 48 may cause the base portion 36 of the fitment 34 to be welded to the neck 14 of the container body 12. In embodiments where the fitment 34 is attached to the neck 14 of the container body 12 by a friction-fit and/or snap-fit connection, the fitment 34 may be inserted into and/or attached to the container body 12 as the closure cap 18 is threaded to the neck 14 of the container body 12. As one example, the attachment extension(s) 160 of the embodiment of
To use the dispensing bottle 10, a user may remove the closure cap 18 and then remove the liner 48 from the fitment 34 and/or the neck 14 of the container body 12. In some embodiments, the closure cap 18 is reattached to the container body 12 and the flip-top lid 28 moved to the open position. The dispensing bottle 10 may then be inverted and squeezed to dispense fluid through the dispensing opening 32 of the closure cap 18. In some embodiments, such as the dispensing bottle 310 of
Uses of singular terms such as “a,” “an,” are intended to cover both the singular and the plural, unless otherwise indicated herein or clearly contradicted by context. The terms “comprising” “having,” “including” and “containing” are to be construed as open-ended terms. It is intended that the phrase “at least one of” as used herein be interpreted in the disjunctive sense. For example, the phrase “at least one of A and B” is intended to encompass A, B, or both A and B.
While there have been illustrated and described particular embodiments of the present invention, those skilled in the art will recognize that a wide variety of modifications, alterations, and combinations can be made with respect to the above-described embodiments without departing from the scope of the invention, and that such modifications, alterations, and combinations are to be viewed as being within the ambit of the inventive concept.
This application claims the benefit of U.S. Provisional Application No. 63/288,363, filed Dec. 10, 2021, which is incorporated by reference in its entirety.
Filing Document | Filing Date | Country | Kind |
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PCT/US2022/052242 | 12/8/2022 | WO |
Number | Date | Country | |
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63288363 | Dec 2021 | US |