Capsule with control member

Abstract

A capsule is provided for use in a machine for preparing a consumable product from capsules. The capsule includes a body that defines an interior space with an opening. Ingredients are disposed within the interior space for preparing a desired product, a portion of the ingredients being non-permanently bound into a cluster. The cluster acts as a control member for controlling a flow of fluid for a period of time within the capsule. A cover is disposed over the opening.

Claims

1. A capsule, for use in a machine that is adapted for injecting a fluid into a capsule for preparing a consumable product, said capsule comprising: a body defining an interior space with an opening; a filter disposed in said interior space to define an ingredients chamber; an axis defined through said opening and said ingredients chamber in said body for receiving an injection of fluid from the machine; insoluble ingredients disposed in said ingredients chamber for preparing a desired consumable product by extraction or infusion from the injection of fluid from the machine, a portion of said insoluble ingredients being non-permanently bound into a cluster that is disposed on the line of said axis; and a cover disposed over said opening.

2. The capsule of claim 1, wherein said cluster comprises compressed ingredients.

3. The capsule of claim 1, wherein said cluster includes a binder material that is adapted to bind said portion of ingredients together.

4. The capsule of claim 3 wherein said ingredients are provided in a dry state and said binder material is provided in a liquid state.

5. The capsule of claim 1, wherein said cluster includes a soluble container that is adapted to contain a portion of ingredients.

6. The capsule of claim 1 wherein said cluster includes a tablet that is adapted to contain a portion of ingredients.

7. The capsule of claim 1, wherein said cluster comprises a first region within said ingredients chamber and at least a portion of the remainder of said ingredients comprises a second region within said ingredients chamber.

8. The capsule of claim 7, wherein said second region at least partially surrounds said first region.

9. The capsule of claim 1, wherein said cluster comprises a non-permanent structure that is adapted to at least partially dissolve or break apart within said capsule when exposed to a flow of fluid over a period of time.

10. The capsule of claim 1, wherein said ingredients comprise roast ground coffee.

11. A capsule, for use in a machine that is adapted for injecting a fluid into a capsule for preparing a consumable product, said capsule comprising: a body defining an interior space with an opening; a filter disposed in said interior space to define an ingredients chamber; an axis defined through said opening and said ingredients chamber in said body for receiving an injection of fluid from the machine insoluble ingredients disposed in said ingredients chamber for preparing a consumable product by extraction or infusion from the injection of fluid from the machine, a portion of said insoluble ingredients forming a control member that is disposed on the line of said axis, wherein said control member comprises a non-permanent structure that is adapted to at least partially dissolve or break apart within said capsule when exposed to the injection of fluid over a period of time; and a cover disposed over said opening.

12. The capsule of claim 11, wherein said control member comprises a cluster formed of compressed ingredients.

13. The capsule of claim 11, wherein said control member comprises a cluster that includes a binder material that is adapted to bind said portion of ingredients together.

14. The capsule of claim 13, wherein said ingredients are provided in a dry state and said binder material is provided in a liquid state.

15. The capsule of claim 11, wherein said control member comprises a soluble container that is adapted to contain said portion of ingredients.

16. The capsule of claim 11, wherein said control member is disposed in a first region within said ingredients chamber and at least a portion of the remainder of said ingredients is disposed in a second region within said ingredients chamber.

17. The capsule of claim 16, wherein said second region at least partially surrounds said first region.

18. The capsule of claim 11, wherein said ingredients comprise roast ground coffee.

19. The capsule of claim 1 wherein said cluster disperses the flow of fluid for a period of time.

20. The capsule of claim 1 wherein said cluster is also disposed along an axis that is transverse to said axis for receiving an injection of fluid from the machine.

21. The capsule of claim 1 wherein said cluster absorbs the flow of fluid for a period of time.

22. The capsule of claim 11 wherein said control member disperses the flow of fluid for a period of time.

23. The capsule of claim 11 wherein said control member absorbs the flow of fluid for a period of time.

Description

DRAWINGS

(1) The drawings included herewith are for illustrating various examples of articles, methods, and apparatuses of the present specification and are not intended to limit the scope of what is taught in any way. For simplicity and clarity of illustration, where considered appropriate, reference numerals may be repeated among the drawings to indicate corresponding or analogous elements.

(2) FIG. 1 is a sectional view of a capsule in accordance with the present invention;

(3) FIGS. 2(a)-2(d) are schematic views of clusters defining control members for a capsule in accordance with the present invention; and

(4) FIG. 3 is a schematic view of a capsule machine for use with a capsule in accordance with the present invention.

DESCRIPTION OF VARIOUS EMBODIMENTS

(5) Various apparatuses or methods will be described below to provide examples of the claimed invention. The claimed invention is not limited to apparatuses or methods having all of the features of any one apparatus or method described below or to features common to multiple or all of the apparatuses described below. The claimed invention may reside in a combination or sub-combination of the apparatus elements or method steps described below. It is possible that an apparatus or method described below is not an example of the claimed invention. The applicant(s), inventor(s) and/or owner(s) reserve all rights in any invention disclosed in an apparatus or method described below that is not claimed in this document and do not abandon, disclaim or dedicate to the public any such invention by its disclosure in this document.

(6) A capsule in accordance with the present invention is shown generally at 10 in the figures. Capsule 10 includes a body 12, filter 14 (when required), ingredients 16 and cover 18. Capsule may be sized to provide a single serving of a desired product or multiple servings.

(7) Ingredients 16 include soluble and/or insoluble ingredients that are a precursor to forming a desired product. Preferably, ingredients 16 are provided in a dry state. Soluble ingredients may include instant coffee, chocolate, soup stock or other ingredients in powdered, crystallized or other forms adapted for solubility or contained within a soluble film or pouch. Insoluble ingredients may include tea leaves, coffee grounds, herbs or other ingredients adapted for forming a consumable product by extraction or infusion. Ingredients 16 may also include active ingredients (eg foaming agents), natural health additives, regulated drugs, alcohol or other soluble or insoluble ingredients.

(8) Ingredients 16 may be disposed in a plurality of distinct regions R1, R2 . . . Rn within capsule 10. The same type of ingredients 16 may be disposed in each region R or different types of ingredients 16 may be disposed in different regions R. The density, cohesion or other physical properties of ingredients 16 may also vary between regions R.

(9) Capsule 10 is sized and configured for use in a machine 20 that is adapted for preparing a product from capsule 10. Machine 20 may include an injection system 22 for injecting a fluid, typically heated water, into the capsule for mixing with ingredients 16. Injection system 22 may include a nozzle 22a disposed on machine 20 that is adapted to pierce cover 18 to inject fluid into capsule 10. Injection system 22 may alternatively have at least one component disposed on capsule 10, such as on cover 18, and adapted to pierce body 12 and interact with machine 20 to inject fluid into capsule 10.

(10) Machine may also include a dispensing system 24 for dispensing product from capsule 10 into a desired receptacle 26 such as a bowl or cup. Dispensing system 24 may include a hollow probe 24a that is adapted to pierce capsule 10 to dispense a prepared product from capsule 10.

(11) Body 12 of capsule 10 includes a sidewall 30 and an end wall 32 together defining an interior space 34. An opening 36 is defined at one end of body 12 and a flange 38 extends around the perimeter of opening 36 to receive cover 18 and to support capsule 10 within machine 20.

(12) In another embodiment, body 12 may be formed with no end wall 32 and no sidewall 30 or a partial sidewall 30. Flange 38 may still extend around the perimeter of opening 36 to receive cover 18 and to support capsule 10 within machine 20. Filter 14 may be secured to flange 38 or to partial sidewall 30.

(13) Filter 14 is adapted to be disposed within body 12 to define at least one ingredients chamber for receiving one or more ingredients 16 and in particular insoluble ingredients 16 that are not intended to be dispensed into receptacle 26 (for example coffee grounds or tea leaves).

(14) Filter 14 is preferably adapted to be phobic to the fluid being injected into capsule 10. In most instances, the fluid will comprise water (either heated or cooled) and a hydrophobic filter 14 is desired. Filter 14 may be formed of materials that are phobic to fluid such as polyolefins (eg, polyethylene, polypropylene) and mixtures of polyolefins with other polymers or filter 14 may be coated with materials that are phobic to fluid such as a polyethylene coating.

(15) Preferably, filter 14 is formed of a moldable non-woven filtration material that includes a plurality of multi-component fibers that are bound or interlocked by non-woven manufacturing techniques (such as spun bond techniques) to form a web having channels extending from one side of filter 14 to the other. The desired diameter for channels after forming is between 20 and 100 m, more preferably between 40 to 80 m. More details of a preferred filtration material for filter 14 are provided in US patent publication 20140127364 which is hereby incorporated in its entirety herein by reference.

(16) Filter 14 may be secured to flange 38 or to an interior surface of capsule 10 (such as to sidewall 30). Capsule 10 may be provided without filter 14 in instances where ingredients are soluble or where it is desired that insoluble ingredients 16 are dispensed together with fluid into receptacle 26 (this requires that dispensing system be adapted to dispense insoluble ingredients 16).

(17) Cover 18 is disposed over opening 36 and secured to body 12 such as by sealing cover 18 directly to flange 38 or indirectly with a portion of filter 14 located between.

(18) A control member 50 may be defined by a cluster 52 of ingredients 16 disposed within capsule 10 as described further below. Control member 50 may comprise a first region R1 of ingredients 16 within capsule 10. The remainder of ingredients 16 for capsule 10 may comprise a second region R2 or capsule 10. Second region R2 may partially or fully surround first region R1. Ingredients 16 in second region R2 may be loosely disposed within capsule while ingredients in first region R1 are contained within cluster 52.

(19) Control member 50 is disposed at a location 54 within capsule 10 that is adapted for controlling the flow of fluid injected into capsule 10. Such fluid control may comprise dispersing a flow of fluid for a period of time, absorbing a flow of fluid for a period of time or otherwise controlling or altering the flow of fluid within capsule 10. Control member 50 comprises a non-permanent structure that is adapted to at least partially dissolve or break apart within capsule when exposed to a flow of fluid over a set period of time (such as the period of time required to inject the desired amount of fluid into capsule 10).

(20) Location 54 is selected according to the type of capsule machine 20 and injection system 22 for which capsule 10 is intended to be used as well as the type of ingredients 16 disposed within capsule 10. Location 54 for K-cup brewers for example may be along a central axis A of capsule 10 in line with the flow of fluid that is injected into capsule 10 through injection nozzle 22a. Location 54 may also be along a transverse axis B where cluster 52 is formed as a layer or crust. In some instances it may be desirable for location 54 to be at a lower portion of capsule 10 and in other instances in may be preferable for location 54 to be at an upper location of capsule.

(21) Cluster 52 comprises a portion of ingredients 16 that are non permanently bound together on their own or with the addition of a binder material. Cluster 52 is adapted to at least partially break apart or dissolve over a desired dwell time T within capsule, when exposed to the flow of fluid in a desired manner from a desired injection system 22.

(22) Cluster 52 may be formed by compressing a portion of ingredients 16 by a desired amount as depicted in FIG. 2(a). The compression can be achieved by a compacting device or an auger system with a relatively high taper which delivers a compacted power to a container. The compression may occur during the process of filling capsule with ingredients or it may occur at a prior stage to filling capsule. Cluster 52 of compressed ingredients is adapted to dissolve or break apart over a period of time when exposed to a flow of fluid within capsule. A cluster 52 of compressed ingredients 16 allows a greater amount of ingredients 16 to be disposed within the same space within capsule 10. Cluster 52 (or region R1) has a higher density of ingredients 16 than ingredients disposed outside of cluster 52 in region R2.

(23) Alternatively, cluster 52 may be formed with a desired binder material 56 as depicted in FIG. 2(b). Binder material 56 is preferably in a liquid state. For example, binder material 56 may be a neutral binder material or it may be an active binder material. A neutral binder material does not add any noticeable flavor, odour, sensory, health benefit or function to the consumable product produced from capsule 10 but may combine or agglomerate with a portion of ingredients 16 to form cluster 52. Examples of neutral binder materials include polyethylene glycol, polypropylene glycol, ethyl alcohol etc. An active binder material provides flavor, odour, sensory, health benefit or function to the consumable product and also may combine or agglomerate with a portion of ingredients 16 to form cluster 52. Examples of an active binder material include Ethyl-2-methybutyrate (apple), 1-octen-3-ol, (mushroom), p-menthene-8-thiol (Grapefruit), 5-methyl-2-hepten-4-one (Hazelnut). The active binder is employed either directly at a high concentration or diluted with a neutral material. Both neutral and active binder materials are preferably highly water soluble.

(24) Alternatively, cluster 52 may be formed with a soluble container 58 that is adapted to contain the portion of ingredients 16 as depicted in FIG. 2(c). For example, soluble container 58 may be formed of soluble gels or films, preferably with water-soluble film. The portion of ingredients 16 contained within soluble container 58 may include liquid ingredients (such as a concentrate) or other ingredients that must be kept separated within capsule (such as foaming agents or other active ingredients).

(25) Preferred materials for soluble container 58 include protein or carbohydrate based materials which could be starch based (e.g., amylose film and amylopectin film), protein based (e.g., gelatin film, casein film), polysaccharide based (e.g., pullulan film, cellulose film), alginate sodium film and pectin film, to name a few. For example, the Vivos edible water soluble film from MonoSol can be employed as a soluble container 58 for ingredients 16. The dissolution rate of soluble container 58, and thus cluster 52, is dependent on the material type. Within the same type, the dissolution rate is normally slower when having heavier material density or molecular weight. Preferably the film thickness for soluble container 58 is in the range of 10-100 m, more preferably 20-80 m and most preferably 30-70 m.

(26) Alternatively, cluster 52 may be provided as a tablet 60 as illustrated in FIG. 2(d). Tablet 60 may contain active or functional ingredients, which can be separated from the rest of ingredients. For instance, a food flavor in a tablet format can be used in this application to add certain flavor into food product.

(27) Control member 50 is sized to control at least a portion of the flow of fluid injected into capsule 10 to other locations within the capsule. Preferably, for a single serve capsule, a single control member 50 has a width in the range of 1 to 25 millimeters and more preferably in the range of 5 to 15 millimeters. Multiple control members 50 comprising one or more types of clusters 52 may be disposed within capsule 10, in which case each control member 50 may have a smaller size.

(28) While the above description provides examples of one or more processes or apparatuses, it will be appreciated that other processes or apparatuses may be within the scope of the accompanying claims.