Process for making a capsule containing a dosing agent

Abstract

A capsule is provided containing a dosing agent and a system and process is provided for making capsules containing a dosing agent. The capsule includes a body defining an interior space and an opening, the capsule having ingredients and a dosing agent disposed in the interior space and a cover to seal the opening. The process and system includes depositing ingredients and the dosing agent in the interior space of the capsule and then covering the opening.

Description

FIELD

This specification relates to capsules containing dosing agents for preparing a desired consumable product and systems and processes for making same.

BACKGROUND

The following background discussion is not an admission that anything discussed below is citable as prior art or common general knowledge. The documents listed below are incorporated herein in their entirety by this reference to them.

Capsules for use in machines to prepare a desired consumable product are becoming increasingly popular. Such capsules come in a variety of formats containing ingredients for producing consumable products such as coffee, tea, hot chocolate or soup.

Capsule machines typically include an injection system for injecting a fluid, such as hot water, into a capsule for mixing with ingredients disposed within the capsule to prepare a desired consumable product. A dispensing system may also be provided to dispense the prepared product from the capsule for delivery to a receptacle such as a user's cup or bowl.

A problem with conventional capsules is that it can be difficult to control the manner in which ingredients are exposed to fluid that is injected into the capsule. It may be desirable for example for certain ingredients to be mixed with fluid within the capsule for a longer period of time than other ingredients. It may also be desirable for certain ingredients to be separated from other ingredients within the capsule prior to, or for a desired period following, injection of fluid into the capsule.

Another problem with conventional capsules is that the fluid injected into the capsule may form one or more channels through the ingredients contained within the capsule along one or more axes of injection. This can result in fluid being dispensed from the capsule prior to adequately mixing with ingredients.

Furthermore, some ingredients may not be sufficiently saturated with fluid to optimize the preparation of the desired product.

It is known to provide permanent structural elements within a capsule to manage the flow of fluid that is injected into the capsule. A problem with permanent structural elements is that they add to the cost and complexity of manufacturing the capsule. Permanent structural elements may also occupy space within the capsule which may be better utilized for other purposes.

It is desirable on occasion that a dosing agent, such as a flavoring component, is added to the capsule to produce a desired consumable product. Dosing agents are typically mixed with ingredients in large totes prior to loading the mixture into capsules.

A problem with this system is that a large number of totes are required in order to have an inventory of different mixtures to produce a desired batch of capsules. Alternatively, if only one or a few totes were available, the tote or totes need to be thoroughly cleaned after each use to prevent mixing of dosing agents.

There is a need for an improved capsule and an improved system and process for making capsules with a desired dosing agent.

SUMMARY OF THE DISCLOSURE

In one aspect, there is provided a process for making a capsule for use in a machine for preparing consumable products from capsules, the process comprising the steps of:

• • providing a body having an interior space and an opening;
  • depositing ingredients that are in a dry state into the interior space, the ingredients being adapted to form a consumable product when combined with fluid;
  • dispensing a dosing agent that is in a liquid state into the interior space; and
  • sealing the opening with a cover.

In another aspect, there is provided a system for making a capsule for use in a machine for preparing consumable products from capsules, the system comprising:

an ingredient station for depositing ingredients that are in a dry state into a body for the capsule, said body having an interior space and an opening, the ingredients being adapted to form a consumable product when combined with fluid;

a dosing agent station for dispensing a dosing agent that is in a liquid state into the interior space of the capsule; and

a cover sealing station for sealing a cover over the opening.

In another aspect, there is provided a capsule made according to the above described process.

In another aspect, there is provided a capsule, for use in a machine for preparing consumable products from capsules, said capsule comprising:

• • a. a body defining an interior space with an opening;
  • b. a filter disposed in said interior space to define an ingredients chamber, said filter being adapted for filtering ingredients during preparation of said consumable product;
  • c. a dosing agent disposed on a portion of said filter for controlling the flow of fluid through said filter;
  • d. ingredients disposed in said ingredients chamber for preparing a desired consumable product; and
  • e. a cover disposed over said opening.

In another aspect there is provided a capsule, for use in a machine for preparing consumable products from capsules, said capsule comprising:

• • a. a body defining an interior space with an opening;
  • b. ingredients disposed in said interior space for preparing a desired consumable product;
  • c. a dosing agent disposed in said interior space with said ingredients, wherein a portion of said ingredients and said dosing agent are non-permanently bound to form a cluster for controlling the flow of fluid through said filter; and
  • d. a cover disposed over said opening.

Other aspects and features of the teachings disclosed herein will become apparent to those ordinarily skilled in the art upon review of the following description of specific examples and the accompanying drawings.

BRIEF DESCRIPTION OF THE DRAWINGS

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.

FIG. 1 is a vertical cross-section of a capsule containing a dosing agent;

FIG. 2 is schematic view of a machine for preparing consumable products from capsules;

FIG. 3 is a schematic view of a dispenser for dispensing a dosing agent into a capsule;

FIG. 4 is a schematic view of a system for making capsules containing a dosing agent;

FIG. 5 is a diagram of a process for making capsules containing a dosing agent;

FIG. 6 is a top view of a capsule without ingredients showing a dosing agent applied to a portion of the filter; and

FIG. 7 is a sectional view of a capsule having a cluster formed as a layer within the ingredients.

DESCRIPTION OF VARIOUS EMBODIMENTS

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.

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.

Ingredients 16 include soluble and/or insoluble ingredients that are a precursor to forming a desired product when combined with fluid as described further below. 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 (e.g., foaming agents), natural health additives, regulated drugs, alcohol or other soluble or insoluble ingredients.

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.

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.

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.

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.

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.

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).

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 (e.g., 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.

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 μm, more preferably between 40 to 80 μm. 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.

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).

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 as described in US patent publication 20130209618 which is incorporated herein in its entirety by reference.

A dosing agent 40, preferably in a liquid state, is disposed within capsule 10 by means of a dispenser 50 (see FIG. 3) prior to completion and sealing of capsule 10 as described further below. Dosing agent 40 may be a neutral dosing agent 40a or it may be an active dosing agent 40b. A neutral dosing agent 40a does not add any noticeable flavor, odour, sensory, health benefit or function to the consumable product produced from capsule 10 but may combine with a portion of ingredients 16 to form a cluster 52 inside capsule 10 as described further below. Examples of neutral dosing agent 40a include polyethylene glycol, polypropylene glycol, ethyl alcohol etc. Conversely, an active dosing agent 40b provides a flavor, odour, sensory, health benefit or function to the consumable product and may also combine with a portion of ingredients 16 to form cluster 52. Examples of active dosing agents 40b include flavor components such as Ethyl-2-methybutyrate (apple), 1-octen-3-ol, (mushroom), p-menthene-8-thiol (Grapefruit) or 5-methyl-2-hepten-4-one (Hazelnut). Active dosing agent 40b is employed either directly at a high concentration or diluted with a neutral dosing agent 40a. Both neutral and active dosing agents are preferably highly water soluble.

In one embodiment, dosing agent 40 is applied to ingredients 16 disposed in capsule 10 in a manner that creates a cluster 52 formed of an agglomeration of a portion of ingredients 16 and dosing agent 40. Cluster 52 may be formed as a clump or as a layer or crust formed of dosing agent 40 and ingredients 16. Cluster 52 comprises a non-permanent structure that is adapted to at least partially dissolve or break apart within capsule 10 when exposed to a flow of fluid over a period of time (such as the period of time required to inject the desired amount of fluid into capsule 10). In one embodiment of the capsule 10, the main beverage ingredient is ground coffee and dosing agent 40 is in the form of an oil or an oil-like product.

Cluster 50 may comprise a first region R1 of ingredients 16 and dosing agent 40 disposed within capsule 10. The remainder of ingredients 16 for capsule 10 may comprise a second region R2 of 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 10 while ingredients 16 and dosing agent 40 in first region R1 are formed into cluster 52.

As shown in FIG. 1, cluster 52 is preferably disposed at a desired 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. Location 54 may be 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. Alternatively, location 54 may 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 10.

Referring to FIG. 3, dispenser 50 comprises a device for dispensing dosing agent 40 in a desired manner and location within capsule 10. In one embodiment, dispenser 50 comprises a nozzle 60, a fluid body 62, a fluid inlet 64, a gas cylinder body 66 and a gas inlet 68 for dispensing a mix of dosing agent 40 and a gas into capsule 10. Fluid body 62 is adapted to receive dosing agent 40 through fluid inlet 64 from a dosing agent supply tank (not shown). Gas cylinder body 66 is adapted to receive a desired gas through gas inlet 68 from a gas supply tank (not shown). Gas and dosing agent 40 are mixed within dispenser 50 and dispensed as a pressurized stream or spray through nozzle 60. In other embodiments, dispenser 50 may dispense dosing agent 40 through nozzle 60 without mixing with a source of gas. In such embodiments, dispenser 50 comprises a fluid body 64 and fluid inlet 64 connected to nozzle 60.

Dosing agent 40 may be applied to ingredients 16 by inserting nozzle 60 partway into ingredients 16 to form cluster 52. Alternatively, dosing agent 40 may be dispensed under pressure over the surface of ingredients 16 without inserting nozzle 60 into ingredients 16. This latter approach avoids direct contact between nozzle 60 and ingredients 16. Dispensing dosing agent 40 under a desired pressure over the surface of ingredients 16 still allows cluster 52 to be formed at a desired location 54 based on factors such as the dispensing pressure of dosing agent 40 and the density of ingredients 16. Alternatively, dosing agent 40 may be applied by dispenser 50 to filter 14 or sidewall 30 or endwall 32 of capsule 10 prior to adding ingredients 16. Alternatively, capsule 10 may be partially filled with ingredients 16 and then dosing agent 40 may be applied to ingredients 16 and then the remaining ingredients 16 may be added to capsule.

Referring to FIGS. 4 and 5, schematic views of a system 100 and a process 1000 for making capsules 10 is shown.

System 100 comprises at least one transfer belt 102 having a plurality of capsule holders 103 adapted to cyclically and sequentially transfer capsules 10 from a working station to a following station as described further below. While only a single capsule holder 103 is shown at each station for system 100 it will be understood that transfer belt 102 has multiple capsule holders 103 disposed at each station in order that manufacturing operations may be performed simultaneously on multiple capsules at each station.

System 100 includes a body forming station 104 for engaging a sheet of moldable multilayered body material 106 with a heated mandrel 108 to form body 12 in accordance with body forming step 1002. Capsule holder 103 with body 12 formed in body material 106 is then transferred to a filter sealing station 110 (if a filter 14 is desired, otherwise capsule holder 103 with body 12 is transferred directly to cutting station 120 as described below). A sheet of moldable nonwoven filter material 112 is sealed to body material 106 at filter sealing station 110 in accordance with filter sealing step 1004 such that filter material 112 covers opening 26 of body 12.

Capsule holder 103 with filter material 112 sealed to body material 106 is then transferred to a filter forming station 116 where a heated mandrel 118 engages the portion of filter material 112 that extends over opening 26 of body 12 to form a filter 14 into a desired shape to define an ingredients chamber 46 within thermoformed body 12 in accordance with filter forming step 1006.

Capsule holder 103 with filter material 112 sealed to body material 106 and filter 14 formed in body 12 is then transferred to a cutting station 120 where a die 122 cuts each individual body 12 with filter 14 from body material 106 in accordance with cutting step 1008. Die 122 is adapted to cut body material 106 to define flange 28 around opening of body 12 with a gasket portion of filter 14 sealed to the top surface of flange 28.

Capsule holder 103 with separated body 12 with filter 14 is then transferred to an ingredients station 124 having an ingredients supplier 126 for supplying a desired amount of ingredients 16 into ingredients chamber 46 in accordance with ingredients loading step 1010. A scale 128 weighs beverage capsule 10 to ensure that the desired amount of ingredients 16 have been disposed into ingredients chamber 46.

Capsule holder 103 then transfers body 12 with filter 14 and ingredients 16 to dosing agent station 130 having a dispenser 50 for dispensing a desired amount of dosing agent 40 into ingredients 16 in accordance with dosing step 1012.

A desired amount of liquid dosing agent 40 for a single serve capsule having 8-10 grams of dry ingredients 16 is in the range of 0.2-2.0 cc. Dosing agent 40, alone or in combination with a gas, can be expelled through nozzle 60 of dispenser 50 into capsule 10. Typically the gas is an inert gas such as nitrogen, not air, in view of the need to keep oxygen away from certain types of ingredients 16 such as roasted ground coffee. In one embodiment, for producing capsules 10 containing loosely filled dry ground coffee or tea, dosing agent 40 is delivered under pressure at a preferred range of 10-50 psi and the dosing time is approximately 0.1 to 0.2 seconds. The amount of dosing agent 40 that is dispensed can be adjusted through varying the orifice size of the nozzle 60, through controlling the time of injection and/or through controlling pressure.

Following dosing step 1012, capsule holder 103 then transfers body 12 with filter 14 and ingredients 16 with dosing agent 40 to cleaning station 132 where a vacuum conduit 134 cleans the exposed surface of flange 28 or gasket portion 50 of filter 14 in preparation for sealing with cover 18 in accordance with cleaning step 1014.

Capsule holder 103 then transfers body 12 with filter 14 and ingredients 16 with dosing agent 40 to a cover pre-sealing station 136 for receiving a supply of a cover material 138 and pre-sealing a portion of cover 18 to gasket portion 50 of filter 14 and to flange 28 of body 12 in accordance with pre-sealing step 1016. Cover pre-sealing station 136 leaves openings 188 along edge of cover 18 for allowing air to be evacuated and inert gas to be flushed into capsule during the modified atmosphere packaging (MAP) process step 1018 as described in more detail below.

Partially sealed capsules 10 are then transferred from capsule holders 103 in transfer plate 102 to corresponding capsule holders 176 disposed within a transfer plate 178 using a pick-and-place device (not shown) or other suitable mechanism. Capsule holders 176 and transfer plate 178 are specially adapted for use during the MAP process step 1018.

Transfer plate 178 with partially sealed beverage capsules 10 disposed in capsule holders 176 is then moved to a MAP station 170 for execution of the MAP process step 1018 as described in more detail in US patent publication 20140141128 which is incorporated herein in its entirety by reference. Once the MAP process is complete, openings 188 in cover 18 are sealed with sealer 192 in accordance with sealing step 1020 and the finished capsule 10 is transferred using a pick-and-place device (not shown) or other suitable mechanism to a collection station 140 for subsequent packaging into boxes (not shown).

It will be understood that system 100 and process 1000 do not require all stations and steps to be provided. It will also be understood that the relative position of stations or the order of process steps may be changed depending on the desired structure and contents of the finished capsule 10.

For example, dosing agent 40 may be sprayed by means of dispenser 50 onto filter 14 as shown in FIG. 6 before ingredients 16 are loaded into capsule. Dosing agent 40 may be selected to provide a layer over a portion of filter to control the flow of fluid through filter. Dosing agent 40 may be formed of a soluble or insoluble material depending on how one wishes to control the flow of fluid through filter.

In another example, dosing agent 40 may be applied to the surface of ingredients 16 that are loaded into capsule 10 to form cluster 52 as a layer or crust of agglomerated ingredients 16. As shown in FIG. 7, a portion of ingredients 16 may be loaded into capsule 10, followed by an application of dosing agent 40 to form cluster 52 and then followed by the remainder of ingredients 16. It will be understood that the stations and process steps may be changed to allow for partial loading of ingredients 16, followed by dispensing of dosing agent, followed by loading of the remaining ingredients 16.

While the above description provides examples of one or more beverage capsules and processes for manufacturing same, it will be appreciated that other beverage capsules and processes may be within the scope of the accompanying claims.

Claims

1. A process for making a capsule for use in a machine for preparing consumable products from capsules, the process comprising the steps of: providing a body having an interior space and an opening;depositing ingredients that are in a dry state into the interior space, the ingredients being adapted to form a consumable product when combined with fluid;dispensing a dosing agent that is in a liquid state into the interior space; andsealing the opening with a cover,wherein said dosing agent is mixed with a gas prior to dispensing into said interior space.

2. A process according to claim 1 wherein a portion of said ingredients and said dosing agent are non-permanently bound into a cluster in said interior space.

3. A process according to claim 2 wherein said cluster is disposed at a location within said interior space that is adapted for controlling a flow of fluid that is injected into said capsule by the machine.

4. A process as claimed in claim 2 wherein said cluster is adapted to at least partially dissolve or break apart over a period of time within said capsule when exposed to a flow of fluid that is injected into said capsule by the machine.

5. A process as claimed in claim 2 wherein said cluster comprises a first region within said interior space and at least a portion of the remainder of said ingredients comprises a second region within said interior space.

6. A process as claimed in claim 5 wherein said second region at least partially surrounds said first region.

7. A process according to claim 1 wherein the dosing agent is dispensed under pressure.

8. A process as claimed in claim 1 wherein said dosing agent is dispensed over said ingredients that are disposed in said interior space.

9. A process as claimed in claim 1 wherein said dosing agent is dispensed into said interior space prior to said step of depositing said ingredients into said interior space.

10. A process according to claim 1 further comprising the step of providing a filter into said interior space for filtering at least a portion of said ingredients during preparation of said consumable product.

11. A process as claimed in claim 10 wherein said dosing agent is dispensed onto said filter prior to the step of depositing said ingredients into said interior space.

12. A process as claimed in claim 1 wherein said gas is an inert gas.

13. A process as claimed in claim 1 wherein said dosing agent is a neutral dosing agent that does not add any noticeable flavor, odour, sensory, health benefit or function to the consumable product produced from said capsule.

14. A process as claimed in claim 1 wherein said dosing agent includes an oil product.

15. A process for making a capsule for use in a machine for preparing consumable products from capsules, the process comprising the steps of: providing a body having an interior space and an opening;depositing ingredients that are in a dry state into the interior space, the ingredients being adapted to form a consumable product when combined with fluid;dispensing a dosing agent that is in a liquid state into the interior space; andsealing the opening with a cover,

16. A process according to claim 15 wherein the dosing agent is dispensed under pressure.

17. A process as claimed in claim 15 wherein said dosing agent is a neutral dosing agent that does not add any noticeable flavor, odour, sensory, health benefit or function to the consumable product produced from said capsule.

18. A process as claimed in claim 15 wherein said dosing agent includes an oil product.

19. A process for making a capsule for use in a machine for preparing consumable products from capsules, the process comprising the steps of: providing a body having an interior space and an opening;depositing ingredients that are in a dry state into the interior space, the ingredients being adapted to form a consumable product when combined with fluid;mixing a dosing agent that is in a liquid state with a gas;dispensing said mixture of dosing agent and gas into the interior space; andsealing the opening with a cover.

20. A process as claimed in claim 19 wherein said gas is an inert gas.

21. A process as claimed in claim 19 wherein said dosing agent is a neutral dosing agent that does not add any noticeable flavor, odour, sensory, health benefit or function to the consumable product produced from said capsule.

22. A process as claimed in claim 19 wherein said dosing agent includes an oil product.

23. A process according to claim 19 wherein the dosing agent is dispensed under pressure.