This disclosure relates to a container comprising a compartment and a closure, which hermetically seals the compartment. The closure comprises an active insert device, which when excited by an external energy source delivers a gas to the compartment to increase the pressure of the compartment.
To prevent microbial spoilage, a hot fill process is often used to package many food and beverage products at high temperatures to sterilize both the product and container. When the liquid content of the container cools, it contracts and either creates an internal vacuum or causes the container to deform, as by shrinking, buckling or paneling. Currently, plastic bottles are designed with panels, ribs and additional resin to compensate for the contraction and prevent bottle deformation. When the smooth side wall of the bottle is replaced with these panels, flexible packaging shapes and designs are prevented, thereby making label application difficult.
Known approaches to the bottle deformation problem add a gas, such as carbon dioxide or nitrogen, to the bottle after sealing. U.S. Pat. No. 7,159,374 discloses an active insert device that contains a reactant and that is affixed to the bottle cap. After sealing the reactant is initiated to a reaction that produces the gas, which is delivered to a headspace of the bottle. The active insert device includes a membrane that admits moisture from the bottle contents into the active insert device to initiate the reaction. The resulting gas then passes through the membrane into the headspace of the bottle. There is a risk that the membrane will loosen and fall into the bottle and contaminate the bottle contents.
Thus, there is a need for a method that releases gas in a closed container to retain microbial stability without leaving a residue or a device that must be removed at time of consumption.
There is also a need to eliminate buckling or paneling in closed hot filled containers in order to capture decorative, lightweight and flexibility benefits.
There is also a need to sufficiently pressurize a closed hot filled container in order to capture structural benefits without deforming the container.
There is a further need to release ingredients and functional components to closed containers on a time delayed basis to enhance functionality.
There is still another need for a container in which gas can be released to pressurize the container after the container is sealed.
There is yet another need for a closure or cap for a container that can release gas into the container after sealing to pressurize the container.
There is yet a further need to substantially eliminate any residue from the active insert device from entering the compartment.
In one embodiment the container of the present disclosure comprises a compartment and a closure that hermetically seals the compartment. An active insert device is disposed in the compartment and comprises one or more reactants that when initiated enter into a diazotization reaction to produce and deliver a gas to the compartment, thereby increasing a pressure of the compartment.
In another embodiment of the container of the present disclosure, a first one of the reactants comprises a primary amine selected from the group of R—NH2, where R is selected from the group consisting of: normal alkyl amines, aromatic amines, amides, and salts of sulfamates.
In another embodiment of the container of the present disclosure, the primary amine is selected from the group consisting of: sodium sulfamate, n-propyl amine, anilene, propylamide, and o-propyl sulfamate.
In another embodiment of the container of the present disclosure, a second of the reactants comprises a proton donor and either a nitrite salt or a nitrite ester.
In another embodiment of the container of the present disclosure, the nitrite salt is selected from the group of the salts of nitrous acid, consisting of: lithium nitrite, sodium nitrite, potassium nitrite, calcium nitrite, and barium nitrite, and wherein the nitrite ester is selected from a group consisting of: nitrite esters of alcohols.
In another embodiment of the container of the present disclosure, the proton donor is any organic acid or any non-organic acid.
In another embodiment of the container of the present disclosure, the organic acid is selected from the group consisting of: mono and dihydrogen citrates, citric, ascorbic, carboxylic and phenolic acids, and wherein the non-organic acid is selected from the group consisting of: hydrochloric, sulfuric and bisulfate.
In another embodiment of the container of the present disclosure, the diazotization reaction is initiated in response to energy provided by an external energy source.
In another embodiment of the container of the present disclosure, the energy creates contact between the reactants and initiates the diazotization reaction.
In another embodiment of the container of the present disclosure, the active insert device further comprises a plurality of layers, wherein the reactant is disposed between first and second layers of the plurality of layers.
In another embodiment of the container of the present disclosure, the active insert device further comprises a filter that filters the gas before delivery to the compartment.
In another embodiment of the container of the present disclosure, the gas is nitrogen. The filter comprises a filter material that retains reaction products of the reaction while allowing the nitrogen gas to be delivered to the compartment.
In another embodiment of the container of the present disclosure, the filter material contains a mixture of permanganate, hydroxide and activated carbon that allows nitrogen gas to be delivered to the compartment while retaining any carbon dioxide, oxides of nitrogen, formaldehyde, acid gases, amines, chlorine, cyanide, nitrates, nitrites and hydrocarbons of the reaction.
In another embodiment of the container of the present disclosure, the filter further comprises the first layer and a third layer of the plurality of the layers. The filter material is disposed between the first and third layer. Each of the first and third layers provides a controlled porosity layer that allows the nitrogen gas to pass through while retaining other products of the reaction.
In another embodiment of the container of the present disclosure, the plurality of layers is disposed on an interior surface of the closure either by bonding or by a retaining element.
In another embodiment of the container of the present disclosure, at least one vent port is disposed in a perimeter portion of at least one of the plurality of layers in fluid communication with the filtered gas.
In another embodiment of the container of the present disclosure, a vent seal that is sealed to the perimeter portion of the plurality of layers to cover the vent port. The vent seal comprises a material of elasticity that under pressure of the filtered gas moves the vent seal away from the at least one layer thereby opening the vent port so that the filtered gas flows into the compartment. Upon equalization of pressure between the active insert device and the compartment, the vent seal flexes back to cover the vent port, thereby preventing any back flow to the active insert device.
In another embodiment of the container of the present disclosure, the vent port is one of a plurality of vent ports disposed in the perimeter portion, and wherein the vent ports are in fluid communication with the filtered gas via a space between the active insert device and the internal surface of the closure.
In another embodiment of the container of the present disclosure, the active insert device further comprises a sealing insert. The plurality of layers is disposed in an interior of the sealing insert.
In another embodiment of the container of the present disclosure, the sealing insert forms a hermetic seal with either or both of an internal surface or a top surface of a neck finish of the container.
In another embodiment of the container of the present disclosure, the active insert device comprises a backing that is hermetically sealed to a lip of the sealing insert such that the interior is hermetically sealed.
In another embodiment of the container of the present disclosure, the sealing insert comprises a bottom with one or more vent ports in fluid communication with the gas.
In another embodiment of the container of the present disclosure, the active insert device further comprises a septum seal with one or more vent ports that are disposed either above or below the bottom.
In another embodiment of the container of the present disclosure, the reactant is a first reactant. A second reactant is also disposed between the first and second layers. A third layer of the plurality of layers is disposed between the first and second reactants. The third layer is modified in response to energy provided by the external energy source to expose the first and second reactants to one another and thereby initiate the reaction.
In an embodiment of the method of the present disclosure, a gas is delivered to a container that includes a closure and a compartment. The method comprises:
disposing an active insert device into the compartment, wherein the active insert device comprises one or more reactants;
initiating the reactants into a diazotization reaction to produce a gas; and
delivering the gas to the compartment, thereby increasing a pressure of the compartment.
In another embodiment of the method of the present disclosure, a first one of the reactants comprises a primary amine selected from the group of R—NH2, where R is selected from the group consisting of: normal alkyl amines, aromatic amines, amides, and salts of sulfamates.
In another embodiment of the method of the present disclosure, the primary amine is selected from the group consisting of: sodium sulfamate, n-propyl amine, anilene, propylamide, and o-propyl sulfamate.
In another embodiment of the method of the present disclosure, a second of the reactants comprises a proton donor and either a nitrite salt or a nitrite ester.
In another embodiment of the method of the present disclosure, the nitrite salt is selected from the group of the salts of nitrous acid, consisting of: lithium nitrite, sodium nitrite, potassium nitrite, calcium nitrite, and barium nitrite, and wherein the nitrite ester is selected from a group consisting of: nitrite esters of alcohols.
In another embodiment of the method of the present disclosure, the proton donor is any organic acid or any non-organic acid.
In another embodiment of the method of the present disclosure, the organic acid is selected from the group consisting of: mono and dihydrogen citrates, citric, ascorbic, carboxylic and phenolic acids. The non-organic acid is selected from the group consisting of: hydrochloric, sulfuric and bisulfate.
In another embodiment of the method of the present disclosure, the diazotization reaction is initiated in response to energy provided by an external energy source.
In another embodiment of the method of the present disclosure, the energy creates contact between the reactants and initiates the diazotization reaction.
In another embodiment of the method of the present disclosure, the active insert device further comprises a heat producing element in thermal transfer relationship to the reactant. The source of energy provides electromagnetic energy that induces an electrical current in the heat producing element so as to thermally initiate the diazotization reaction.
In another embodiment of the method of the present disclosure, the active insert device is disposed on the closure. The disposing step comprises fastening the closure to the container.
In another embodiment of the method of the present disclosure, the method further comprises filtering the gas before delivery to the compartment.
In another embodiment of the method of the present disclosure, the gas is nitrogen. The filtering step uses a filter material that retains reaction products of the reaction while allowing the nitrogen gas to be delivered to the compartment.
In another embodiment of the method of the present disclosure, the filter material contains a mixture of permanganate, hydroxide and activated carbon that allows nitrogen gas to be delivered to the compartment while retaining any carbon dioxide, oxides of nitrogen, formaldehyde, acid gases, amines, chlorine, cyanide, nitrates, nitrites and hydrocarbons of the reaction.
In another embodiment of the method of the present disclosure, the gas is delivered to the compartment via at least one vent port. The vent port is closed when a pressure on the active insert device side of the vent port equalizes with a pressure of the compartment so as to prevent back flow.
In an embodiment of the closure of the present disclosure, the closure is for a container having a neck finish and a compartment. The closure comprises a cylinder that is styled for fitting on the neck finish. The cylinder comprises a top having an internal surface. An active insert device, which is disposed in the cylinder, comprises one or more reactants that when initiated enter into a diazotization reaction to produce and deliver a gas to the compartment.
In another embodiment of the closure of the present disclosure, a first one of the reactants comprises a primary amine selected from the group of R—NH2, where R is selected from the group consisting of: normal alkyl amines, aromatic amines, amides, and salts of sulfamates.
In another embodiment of the closure of the present disclosure, the primary amine is selected from the group consisting of: sodium sulfamate, n-propyl amine, anilene, propylamide, and o-propyl sulfamate.
In another embodiment of the closure of the present disclosure, a second of the reactants comprises a proton donor and either a nitrite salt or a nitrite ester.
In another embodiment of the closure of the present disclosure, the nitrite salt is selected from the group of the salts of nitrous acid, consisting of: lithium nitrite, sodium nitrite, potassium nitrite, calcium nitrite, and barium nitrite, and wherein the nitrite ester is selected from a group consisting of: nitrite esters of alcohols.
In another embodiment of the closure of the present disclosure, the proton donor is any organic acid or any non-organic acid.
In another embodiment of the closure of the present disclosure, the organic acid is selected from the group consisting of: mono and dihydrogen citrates, citric, ascorbic, carboxylic and phenolic acids. The non-organic acid is selected from the group consisting of: hydrochloric, sulfuric and bisulfate.
In another embodiment of the closure of the present disclosure, the diazotization reaction is initiated in response to energy provided by an external energy source.
In another embodiment of the closure of the present disclosure, the energy creates contact between the reactants and initiates the diazotization reaction.
In another embodiment of the closure of the present disclosure, the active insert device further comprises a plurality of layers. The reactant is disposed between first and second layers of the plurality of layers.
In another embodiment of the closure of the present disclosure, the active insert device further comprises a filter that filters the gas before delivery to the compartment.
In another embodiment of the closure of the present disclosure, the gas is nitrogen. The filter comprises a filter material that retains reaction products of the reaction while allowing the nitrogen gas to be delivered to the compartment.
In another embodiment of the closure of the present disclosure, the filter material contains a mixture of permanganate, hydroxide and activated carbon that allows nitrogen gas to be delivered to the compartment while retaining any carbon dioxide, oxides of nitrogen, formaldehyde, acid gases, amines, chlorine, cyanide, nitrates, nitrites and hydrocarbons of the reaction.
In another embodiment of the closure of the present disclosure, the filter further comprises the first layer and a third layer of the plurality of the layers. The filter material is disposed between the first and third layer. Each of the first and third layers provide a controlled porosity layer that allows the nitrogen gas to pass through while retaining other products of the reaction.
In another embodiment of the closure of the present disclosure, the plurality of layers is disposed on the internal surface either by bonding or by a retaining element.
In another embodiment of the closure of the present disclosure, at least one vent port is disposed in a perimeter portion of at least one of the plurality of layers in fluid communication with the filtered gas.
In another embodiment of the closure of the present disclosure, a vent seal is sealed to the perimeter portion of the plurality of layers to cover the vent port. The vent seal comprises a material of elasticity that under pressure of the filtered gas moves the vent seal away from the at least one layer thereby opening the vent port so that the filtered gas flows into the compartment. Upon equalization of pressure between the active insert device and the compartment, the vent seal flexes back to cover the vent port, thereby preventing any back flow to the active insert device.
In another embodiment of the closure of the present disclosure, the vent port is one of a plurality of vent ports disposed in the perimeter portion. The vent ports are in fluid communication with the filtered gas via a space between the active insert device and the internal surface of the closure.
In another embodiment of the closure of the present disclosure, the active insert device further comprises a sealing insert. The plurality of layers is disposed in an interior of the sealing insert.
In another embodiment of the closure of the present disclosure, the sealing insert forms a hermetic seal with either or both of the internal surface of the cylinder or a top surface of a neck finish of the container.
In another embodiment of the closure of the present disclosure, the active insert device comprises a backing that is hermetically sealed to a lip of the sealing insert such that the interior is hermetically sealed.
In another embodiment of the closure of the present disclosure, the sealing insert comprises a bottom with one or more vent ports in fluid communication with the gas.
In another embodiment of the closure of the present disclosure, the active insert device further comprises a septum seal with one or more vent ports that is disposed either above or below the bottom.
In another embodiment of the closure of the present disclosure, the reactant is a first reactant. The active device further comprises a second reactant that is also disposed between the first and second layers. A third layer of the plurality of layers is disposed between the first and second reactants. The third layer is modified in response to energy provided by the external energy source to expose the first and second reactants to one another and thereby initiate the reaction.
Other and further objects, advantages and features of the present disclosure will be understood by reference to the following specification in conjunction with the accompanying drawings, in which like reference characters denote like elements of structure and:
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While these arrangements are preferred embodiments, it is possible to conceive of other variations in design that provide the functions described above. In the first, second and third embodiments, the function of active insert device 201, 1201 or 2201 is to control the generation, purification and release of a gas 403, 1403 or 2403 into container headspace 402, 1402 or 2402 to hermetically inflate and or pressurize container 420, 1420 or 2420. In the first step of the process, functional container closure 100, 1100 or 2100 is screwed onto neck finish 401,1401 or 2401 of container 420, 1420 or 2420 with a suitable torque to create a hermetic seal between vent seal 309 and the neck finish 401 or between sealing insert 1311 or 2311 and neck finish 1401 or 1401.
Referring again to the first, second and third embodiments, in the second step of the process, metallic inductor 306, 1306 or 2306 is heated by means of a current flow induced in it through the application of external electromagnetic energy 404, 1404 or 2404 provided by an external energy source 430, 1430 and 2430 as shown in
Filter medium 302, 1302 or 2302 is designed to capture, retain and or convert certain vapors and gases and prevent them from passing through the backing membrane 301, 1301 or 2301 while allowing the desired components including desired gases 403, 1403 or 2403 to pass through the backing membrane 301, 1301 or 2301.
Referring to the first embodiment, the desired gas 403 passes between backing membrane 301 and the internal surface 103 of cap 101 thereby creating a pressure point at one or more vent ports 202. The pressure of gas 403 trying to pass through one or more vent ports 202 causes vent seal 309 to release its bond to shroud 308 and separate in the area of vent port 202. The small separation allows gas 403 to pass into headspace 402. Gas 403 continues to pass through into headspace 402 until the pressure in headspace 402 equalizes with the pressure being generated inside the active insert device 201. At this point, vent seal 309 stretches back into its original position, closing the separation between itself and shroud 308 and again creating a hermetic seal that prevents a reverse flow through one or more vent ports 202.
Referring to the second embodiment, the desired gas 1403 passes through backing membrane 1301 and exits sealing insert 1311 through perforations 1315. The exiting gas 1403 from perforations 1315 creates a pocket behind septum seal 1312 thereby allowing score marks 1314 to open and allow gas 1403 to vent into headspace 1402. Once the pressure in the headspace 1402 equalizes with that inside sealing insert 1311, septum seal 1312 returns to its original state and the score marks close thereby sealing off headspace 1402 from insert device 1201.
Referring to the third embodiment, the desired gas 2403 passes through backing membrane 2301 and pushes down on septum seal 2312 thereby allowing score mark 2314 to open and allow gas 2403 to exit sealing insert 2311 through vent ports 2320 and vent into headspace 2402. Once the pressure in headspace 2402 equalizes with that inside sealing insert 2311, septum seal 2312 returns to its original state and score marks 2314 close thereby sealing off headspace 2402 from insert device 2201.
It will be apparent to those skilled in the art that many other embodiments may be conceived of that would result in the same outcome as those intended and contemplated within this disclosure. Therefore, without reference to any specific figure, the following should be noted. The first reactant 307, 1307 or 2307 and the second reactant 304, 1304 or 2304 can be made up of any substance or mixture of substances (in any phase, solid, liquid or vapor) that when coming into contact with one another causes a reaction to take place that produces a third product or products that are desirable for the specific function for which the functional closure device is designed.
In the inflation and or pressurization embodiment described above, the reactants are selected for a diazotization reaction. First reactant 307, 1307 or 2307 is a primary amine, which is defined as an ammonia molecule with one hydrogen substituted by any organic or inorganic compound, usually represented by R; for example, R—NH2, where the primary amine can be selected from the following groups: normal alkyl amines (CH3(CH2)n—NH2, where CH3(CH2)n— represents straight-chain, normal alkyl groups of any length), for example, n-propyl amine; aromatic amines (AR-NH2, where AR represents any aromatic compound) for example aniline; amides (RCO—NH2, where RCO— represents any acyl group) for example propylamide; salts of sulfamates (XOSO2—NH2, where X represents any cation), for example, sodium sulfamate, and O-substituted sulfamates (ROSO2—NH2, where R represents any organic compound), for example, o-propyl sulfamate.
Second reactant 304, 1304 or 2304 of the diazotization comprises a nitrite salt and a proton donor, or a nitrite ester and a proton donor. The nitrite salt can be selected from the group of the salts of nitrous acid, XNO2 (where X represents any cation), for example, lithium nitrite, sodium nitrite, potassium nitrite, calcium nitrite, and barium nitrite. An example of a group of nitrite esters is the nitrite esters of alcohols. One example is ethyl nitrite (CH3CH2ONO), which is the nitrite ester of ethyl alcohol. The proton donor is any organic acid, for example, mono and dihydrogen citrates, citric, ascorbic, carboxylic and phenolic acids, or any non-organic acid, such as mineral acids, for example, hydrochloric, sulfuric and bisulfate.
When external energy 404, 1404 or 2404 is incident on active insert device 201, 1201 or 2201, a reaction of the nitrite salt and the proton donor forms nitrous acid and ultimately a nitrosonium ion (NO+). The nitrosonium ion reacts with the primary amine to produce an unstable diazonium intermediate, which readily decomposes in nitrogen gas. In this preferred embodiment, first reactant 307, 1307 or 2307 is preferably sodium sulfamate and second reactant 304, 1304 or 2304 is preferably sodium nitrite and di-sodium citrate. Other substances in the reactants may include but are not limited to catalysts, filers, binders, surfactants and antifoaming agents that do not participate directly in the reaction but provide other functionality such as catalyzing, enhancing and controlling the rate of reaction and or retaining certain reactant mixtures and reaction products.
Filter membrane 303, 1303 or 2303, filter media 302, 1302 or 2302 and backing membrane 301, 1301 or 2301 together form a filter system designed to capture, retain or filter out any undesirable reaction products. Filter media 302, 1302 or 2302 can be any substance or mixture of substances designed for the adsorption, absorption, oxidation, reduction or other reaction, retention and/or alteration of the characteristics of any specific reaction products or byproducts for which the functional closure device is designed. In the inflation and or pressurization embodiment described above, the filter media contains for example a suitable mixture of permanganate, hydroxide, and activated carbon so that any carbon dioxide, oxides of nitrogen, formaldehyde, acid gases, amines, ammonia, chlorine, nitrates, nitrites and hydrocarbons are converted and retained within the filter system while allowing pure nitrogen gas to pass through into the headspace 402, 1402 or 2402.
An example of a suitable filter media is a mixture of >50% potassium permanganate, <30% Calcium Hydroxide, <20% Activated Carbon, and <2% Sodium Hydroxide, the remainder being made up of fillers and or binders such as Silicon Dioxide SiO2. Other substances in the filter media include but are not limited to filers, binders, activators and catalysts that do not necessarily participate in the filtration process but provide other functionality to the filter system such as, for example, controlling the rate of flow and dispersion of the reaction products and or surface area, concentration and texture of the filter media.
Filter membrane 303, 1303 or 2303 and backing membrane 301, 1301 or 2301 can be any material or composition of materials that provide a controlled porosity layer suitable for the function of allowing certain products or mixtures of products to pass through while retaining or preventing other products or mixtures of products from passing through.
Bond 204 is any suitable bond along the perimeter that joins backing membrane 301, filter membrane 303, separating seal 305 and shroud 308 together. Bond 204 can be formed using adhesives, heat welding or any other hot or cold process that achieves the desired hermetic seal. Bond 310, 1310 or 2310 is any suitable bond between separator seal 305, 1305 or 2305 and metallic inductor 306, 1306 or 2306 that ensures heat transfer between the materials that further allows the separator seal to tear, rupture, delaminate or become cut in a controllable manner.
The securing of active insert device 201 into closure 101 along the perimeter of internal surface 103 can be achieved with any suitable bond that provides a hermetic seal along said perimeter without blocking access to one or more vent ports 202. The bond secures active insert device 201 in such a way that it becomes a single unit with cap 101 and remains in place when cap 101 is removed from neck finish 401. The bond is intended to be achieved such that active insert device 201 cannot be removed non-destructively from the cap 101. This bond can be formed using adhesive or heat welding or any other suitable hot or cold bonding process.
Vent seal 309 can be any material or combination of materials that allow it to become hermetically bonded to the external surface of shroud 308 while still allowing the bond to separate in the area of one or more vent ports 202. This causes vent seal 309 to stretch away from shroud 308 in this area further allowing vent ports 202 to become open under pressure. Upon equalization of pressure between active insert device 201 and headspace 402, vent seal 309 is allowed to flex back over the vent ports 202, thereby closing them and preventing any back flow from the headspace 402 into the active insert device 201. Vent seal 309 also forms a hermetic seal between active insert device 201 and neck finish 401 thereby containing the headspace gases 403 and allowing headspace 402 to become inflated and maintain a positive pressure. In the embodiment described above, vent seal 309 has the property of elasticity and may be constructed from materials selected from the group of saturated and unsaturated rubbers, elastomers and self healing elastomers.
Septum seal 1312 or 2312 can be any material or combination of materials that allow it to act as a septum and allows for score marks to open and close at varying pressure differentials. In the second embodiment described above, the septum seal has the property of elasticity and may be constructed from materials selected from the group of saturated and unsaturated rubbers, elastomers and self healing elastomers.
Bond 1316 or 2316 may be any suitable bond that forms a hermetic seal between the device layers and the sealing insert 1311 or 2311. Bond 1316 or 2316 can be formed using adhesives, heat welding or any other hot or cold process that achieves the desired hermetic seal. Bond 1318 or 2321 is any suitable bond that bonds septum seal 1312 or 2312 to sealing insert 1311 or 2311 and allows it to stretch away and return to its original state. Bond 1318 or 2321 can be formed using adhesives, heat welding or any other hot or cold process that achieves the desired seal.
Internal lip 1421 or 2421 is any lip that creates a seal when contacted with internal surface 1422 or 2422 and can be of any shape, texture or profile that best achieves that outcome. Landing surface 1423 or 2423 is any surface that creates a seal when contacted with landing 1424 or 2424 and can be any shape, texture or profile to achieve that outcome.
The present disclosure having been thus described with particular reference to the preferred forms thereof, it will be obvious that various changes and modifications may be made therein without departing from the spirit and scope of the present disclosure as defined in the appended claims.
This application claims the benefit of U.S. Provisional Application, Ser. No. 61/252,736, filed on Oct. 19, 2009, the entire contents of which are incorporated herein.
Number | Date | Country | |
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61252736 | Oct 2009 | US |