The present novel invention relates generally to the art of cooling food and beverage containers and to processes for manufacturing such containers. More specifically the present invention relates to an apparatus for cooling a food product such as a beverage, means and methods of cooling said containers with said apparatus, including methods of assembling and operating said apparatus. The terms “beverage,” “food,” “food products” and “container contents” are considered as equivalent for the purposes of this application and used interchangeably. The term “food product container” refers to any sealed and openable storage means for a food product meant for consumption.
There previously have been many self-cooling food product container devices for cooling the container contents in the form of a beverage or other food beverage food product container. These devices sometimes use flexible and deformable receptacles or rigid receptacle sides to store a refrigerant for phase change cooling. Some prior art devices use desiccants with a vacuum V activated to evaporate water at low pressure and absorb vapor into a desiccant. Other prior devices use refrigerants stored between pressure vessels in liquid phase to achieve the cooling by causing a phase change of refrigerants from a liquid to a gaseous state. The present inventor has invented a variety of such devices and methods of manufacturing them. Several prior self-cooling food product container technologies rely on the evaporation of a refrigerant from the liquid phase to the gaseous phase. Some rely on desiccants only. Desiccant technologies rely the thermodynamic potential of a desiccant to absorb water from a gaseous phase into the desiccant to effectuate the evaporation of water in a vacuum V. These earlier inventions do not satisfy all the needs of the beverage industry and they do not use electromotive heat transport means to cool a beverage. In fact, they are so structurally different from the present invention, that one skilled in the art cannot possibly transcend from the prior art to the present invention without an inventive process. In an effort to seek a cost effective and functioning apparatus for self-cooling a beverage food product container, the present inventor has done a variety of experiments to arrive at the present novel method. The following issues have kept the cost effective commercialization of all prior art devices prohibitively high.
Prior art that uses liquefied refrigerants fail to address the real issues of manufacturing and beverage plant operations that are crucial for the success of a self-cooling food product container program. Some such prior art designs require pressurized food product containers to store liquid refrigerants. For example, U.S. Pat. No. 4,584,848 to inventor Eugene R. Barnett, uses a double chamber formed or drawn from a slug of metal to store pressurized gases and release them using complicated valves involving a spring and a lance to pierce and allow the pressurized gases to escape and cool by evaporation. In line 61 page 1, the inventor states “The outer chamber has a relatively thin wall, and the inner chamber has a relatively thicker wall”. The inventor also sites a spring and a lance mechanism and in fact the inventor recites that the pressure of the gases used by the apparatus is high by reciting on line 54 and 55 of page 2 “ . . . the coolant emerges from the high pressure in the inner chamber 11b”. Such a device is expensive to make and the cost of springs alone can deter the commercial viability of such devices.
The only liquid refrigerants that can be stored between commercially viable pressure canisters are HFCS, CFCS, hydrocarbons, ethers, and other highly flammable low-pressure gases. These gases are not commercially viable and have led to difficulty in implementation of such technologies. Most commercial refrigerants are ozone depleting and global warming and as such have been banned by the EPA in the USA and other governing bodies for direct release into the atmosphere as products of a self-cooling food product container. The EPA has mandated that no refrigerant be used in a self-cooling food product container except CO2 and if used, the design must be safe. Refrigerants currently available cause both global warming and ozone depletion. Generally, they are common refrigerants such as 134a and 152a. In some cases, flammable gases such as butane and propane have been tried but the risk factors are high for several reasons. Firstly, the use of such technologies in a closed room can cause a variety of effects including asphyxiation, poisoning and so on. Second the flammability of some refrigerants limits the number of food product containers that can be opened in a closed environment such as during parties or in a vehicle. The present inventor has several patents on these prior technologies, has experimented with several of these technologies and has found them to be unsuitable for commercial viability. Further, the cost of refrigerants is very prohibitive and the cost of cooling cannot justify the use of refrigerant gases.
As another example by the present inventor, U.S. Pat. No. 6,170,283 uses an expandable receptacle to store pressurized liquefied gases that can be released to cool a beverage by evaporation of said liquefied gases. However, to reduce costs, the inventor resorts to attaching the receptacle to the rim of the beverage container to separate the beverage from the liquefied gases. On line 53 page 6, the inventor states, “ . . . where liquefied refrigerant 28 is charged into receptacle 30 . . . ”. The intent of this patent was to reduce costs by creating a liquefied storage system that relies of the container itself to withstand the pressure of the liquefied refrigerants. This however requires breakable portions of the receptacle that can also break unintentionally and permitting the refrigerant to contaminate the beverage.
A similar situation is presented by U.S. Pat. No. 3,494,143 to E. R. Barnett et al, where a metal container is jointly crimped with the beverage container lid to generate a double chamber for the beverage and the refrigerants. The inventor resorts to a puncturing tool to activate the apparatus for cooling. On Line 14 page 3, the inventor states, “The puncturing tool 54 is shown as a cone-shaped penetrator or piercing point 56 carried as shown by the lower portion of leaf 58 of a formed piece of resilient sheet-stock, . . . ”. Again, the expense of just forming such a part is prohibitive to the commercialization of a self-cooling container since it involves special manufacturing processes that exceed the cost of even the container itself.
In U.S. Pat. No. 4,669,273, Fischer et al invented a coiled tube insert to cool a beverage within a beverage container by releasing a pressurized liquid refrigerant from the coiled tube to an evaporator to chill the beverage within the container. On line, 32 page 2, the inventor recites, “The coiled tube assembly 15 comprises thin walled coiled tube 15a . . . ”. The cost of a coiled tube that can hold pressurized refrigerants at even carbonation pressures is prohibitive. For example, a ¼ ″ diameter commercial aluminum thin-walled tube can cost about $1.00/foot, and since the coil described by the inventor must hold at least 4 oz of a refrigerant to effectively cool a 12 oz beverage, one would need at least a coil of length of about 129 inches, or about 10 ft. This patent also is plagued with commercial issues since the manufacture of the coiled tube is expensive and requires materials and processes costing far more that it would cost to refrigerate the beverage in a refrigerator over an average period of time of storage before consumption.
Robert R. Holcomb of Alabama revealed in his US patent number 468,8395, a self-contained cooling device for use in a container that includes a reservoir containing a highly pressurized fluid such as CO2. On line 61, page 2, the inventor recites, “The reservoir is preferably pressurized with carbondioxide.” Carbondioxide has a liquefaction pressure of over 800 psi. Such pressures cannot be easily contained in pressure chambers with diameters of 1″ or more without specialized designs and thick walled materials. In fact, the cone design the inventor manifests as operable is counter-intuitive, since it has a pressure profile that changes as its diameter changes along the cone axis. Wall thickness of at least 0.125″ are required by DOT regulations to transport CO2 in commercial pressure canisters. This is far removed from the present invention which teaches the use of extremely low pressure chambers made from bag-like materials to achieve better cooling.
The inventor further teaches that the refrigerant reservoir is secured to the inside of the container to form an expansion chamber between the reservoir and the container. And a tube communicates with the reservoir and extends into the expansion chamber, the tube normally being closed to prevent escape of pressurized fluid from the reservoir. When it is desired to cool the contents of the container the tube is opened so that pressurized fluid from the reservoir expands into the expansion chamber thereby cooling the expansion chamber, reservoir, and contents of the container. This invention also uses sophisticated spring loaded actuators to release the refrigerant for cooling. The cost of such springs are definitely further evidence of the prohibitive nature of such inventions to the commercialization of a self-cooling container.
Further examples of inventions that use pressurized gases are found in U.S. Pat. Nos. 3,494,143, 3,088,680, 4,319,464, 3,241,731, 8,033,132, 4,319,464, 3,852,975, 4,669,273, 3,494,141, 3,520,148, 3,636,726, 3,759,060, 3,597,937, 4,584,848, 3,417,573, 3,468,452, 654,174, 1,971,364, 5,063,754, 3,919,856, 4,640,102, 3,881,321, 4,656,838, 3,862,548, 4,679,407, 4,688,395, 3,842,617, 3,803,867, 6,170,283, 5,704,222 and many others.
Prior art that uses cryogenic refrigerants such as CO2 fail to address the real issues of manufacturing and beverage plant operations that are crucial for the success of a self-cooling food product container program. All such prior art designs require very highly pressurized food product containers to store the cryogenic refrigerants. Some technologies that promise to use CO2 have implemented carbon traps such as activated carbon, and fullerene nanotubes to store the refrigerants in a carbon matrix. These added desiccants and activated carbon storage systems are too expensive to implement commercially and further, the carbon and other absorptive media that lowers the pressure can contaminate the beverage products. Therefore, there is a need to reduce the quantities of such chemicals needed. Cryogenic self-cooling food product containers require the use of very high pressure vessels, and cryogenic gases such as CO2, and they also require expensive containers made from high pressure bearing materials such as aluminum, steel, or fiber-glass. They are essentially dangerous, since the pressures involved are generally of the order of 600 psi or more.
Desiccant-based self-cooling food product containers require the desiccant to be stored in a an evacuated chamber separated fluidly from water stored in a separate chamber. When the vacuum is released between the two compartments, water vapor is pulled into the vacuum and then absorbed by the desiccant and heat of evaporation is taken from the cooled item and transported to condense in the desiccant. The heat taken by the evaporated water heats up the desiccant and must not be permitted to interact with the beverage, otherwise it would reheat the beverage again. It is very difficult to maintain for a long period a true vacuum in chamber adjacent to a water containing chamber since the permeability of the barrier used to separate the desiccant chamber from the water chamber contributes to the efficiency of cooling, and the thicker the barrier required the more expensive it becomes to manufacture. Further, the valves and activation devices used by prior art using a desiccant cooling means require stiff pins, knives, and so on. Further, the vacuum must be maintained for a long period of storage time and often fails. Migration of moisture into the desiccant can destroy the cooling capacity of such devices. Further, it is extremely difficult to handle desiccant crystals the way prior art designs are implemented, and powders in a mass-manufacturing environment where the desiccant has to be maintained moisture free and contaminant-free inside a pressurized beverage food product container is extremely difficult to realize. Thus a better technology is needed to handle these desiccants separately from the food product container. Further, the heat absorption potential of desiccants reduces as the vacuum is released and evaporation starts and the process becomes inefficient by itself and becomes limited to the amount of desiccant used.
The problems presented by vacuums, including difficulties in creating and maintaining them and the lack of efficiency have been encountered in other fields as well. An early example can be found in the evolution of Thomas A. Edison's light bulb. His first practical incandescent lamp, for which he received a patent in 1879, included a carbonized bamboo filament contained within an evacuated glass bulb. Although it arguably propelled the world into a new era, it was initially highly inefficient. Then in 1904, European inventors replaced the carbonized bamboo filament with tungsten, and in 1913 it was discovered that replacing the vacuum within the bulb with an inert dry gas doubled its luminous efficiency. Although this field of art is different from the present one, and the technical issues presented were quite different, this is perhaps a thought provoking example of an advance in product efficiency resulting from the replacement of a vacuum with a dry gas.
In general, these prior art technologies are not cost-effective technologies and they rely on extremely large and complicated canister designs in relation to the beverage food product containers within which they are contained. In fact, the ratio of desiccant to water is about 3:1 and the ratio of the volumetric loss in such beverage food product containers is about 40%. The cost of the desiccant or sorbent, the cost of the food product container, and the cost of the process of manufacture are prohibitive, despite nearly 20 years of trials. Thus it is advantageous to reduce the amounts of these components needed and to restructure the manufacturing process to divorce the interior of the food product container from these chemicals.
For example, U.S. Pat. No. 7,107,783 to Smolko et al, discloses self-cooling containers using desiccants that comprise porous matrices as elements of the container bodies to effect the cooling of contained liquids by pervaporation. On line The liquid vapor can pass through the porous matrix directly to the environment or to a collector or trap comprising an absorbent material in contact with the container. The porous desiccant matrix is contained in a sleeve-like container that surrounds the beverage. The cost of manufacture of such sleeves is prohibitive for commercialization of such devices and they also require careful use of porous matrices that can be delicate and brittle. Further, such porous matrices are prone to absorption of atmospheric gases which render such devices inert without a vacuum. Vacuums are very difficult to maintain in pressurized carbonated beverages over a period of time. As another example, Siegel; Israel (North Miami Beach, FL) reveled in U.S. Pat. No. 4,928,495 self-cooling and self-heating beverage containers utilizing water, the boiling point of which has been lowered by a vacuum as the working cooling fluid. A desiccant placed in a separate container sorbs the vapor generated by the boiling water at a low pressure to cool the beverage. This invention also requires a vacuum that has to be stored over a period of time and as such are prone to failure due to the difficulty of maintaining a vacuum over time. Further the invention requires several components and several interconnected means for actuation rendering it impractical for commercialization purposes. Another example is provided by Stewart Molzahn of Bass brewers in U.S. Pat. No. 6,141,970. His invention again relies on a vacuum which is stored within the desiccant chamber separated from water in a separate chamber by a thin membrane. Suffice it to say that such membranes can leak over time and render the apparatus useless over a short period of time. Further, a vacuum required the use of very stiff storage members that become cost prohibitive for commercialization of such devices.
Further examples of devices that use this technology are found in U.S. Pat. Nos. 7,107,783, 6,389,839, 5,168,708, 6,141,970, 829,902,4, 462,224, 7,213,401, 4,928,495, 4,250,720, 2,144,441, 4,126,016, 3,642,059, 3,379,025, 4,736,599, 4,759,191, 3,316,736, 3,950,960, 2,472,825, 3,252,270, 3,967,465, 1,841,691, 2,195,0772, 322,617, 5,168,708, 5,230,216, 4,911,740, 5,233,836, 4,752,310, 4,205,531, 4,048,810, 2,053,683, 3,270,512, 4,531,384, 5,359,861, 6,141,970, 6,341,491, 4,993,239, 4,901,535, 4,949,549, 5,048,301, 5,079,932, 4,513,053, 4,974,419, 5,018,368, 5,035,230, 6,889,507, 5,313,799, 6,151,911, 6,151,911, 5,692,381, 4,924,676, 5,038,581, 4,479,364, 4,368,624, 4,660,629, 4,574,874, 4,402,915, 5,233,836, 5,230,216. U.S. Pat. No. 5,983,662 uses a sponge in place of a desiccant to cool a beverage.
Prior art also reveals chemically endothermic self-cooling food product containers. These rely on the use of fixed stoichiometric reactions of chemicals to absorb heat from the food product container contents. U.S. Pat. No. 3,970,068, to Shataro Sato reveals a heat exchange packaging that uses chemicals to cool and heat food products respectively. However, Shataro Sato reveals an invention that uses two chambers isolated from one another by a barrier that can be pierced by a needle to mix the reactants to cool or heat a food product. On line 64 page 2, he states, “said needle-member 23, as shown c) in
U.S. Pat. No. 2,300,793 to V. E. C Martin reveals a dual container for heating a products using reactants. Again on line 43 page 2 he states, “The medial portion of can bottom 5 may then be given a sharp blow or blows to force punch 19 to pierce or puncture the partition1.” This actuation means revealed by several inventors including Martin is indeed cost prohibitive and the method reveals one of the reasons why all such prior inventions have been unsuccessful commercially.
Other patents such U.S. Pat. No. 7,117,684 to Scudder, et al., reveals an endothermic cooling process for self-cooling containers. Scudder also reveals a means of activation of his device using a piercing device to break a barrier between two reactants. On line 59, page 1, he states, “Depressing the actuator button forces the prong into the barrier, puncturing it thereby allowing the liquid reactant to flow into the solid reactant in the reaction chamber.” Once again, the piercing technic is used to mix chemical reactants at the cost of commercialization. The cost of manufacturing the piercing device is prohibitive and added to this cost is the complicated pleated design of the reaction chamber and entire apparatus according to Scudder.
U.S. Pat. No. 4,993,237 to Bond, et al. also reveals a similar method to the method revealed by Scudder et al., for an endothermic cooling system. Bond reveals a method that uses a long member to break a seal when the opening means of the conventional can is used to open the can. In line 58, page 3, Bond states, “The initialization rod 20 is long enough to extend substantially to the breakaway seal 18 shown in
When I worked as a volunteer aid in Africa, a metal rod to from a machine entered a local brewery's bottling line and infiltrated a beer bottle. A friend of mine was unfortunate enough to get this particular bottle and was nearly hospitalized, were it not for the kind work of a local doctor.
U.S. Pat. No. 3,229,478 to Jose Alonso also reveals a self-cooling container with a valve device and a vacuum chamber for actuating the apparatus. On line 1 page 3, Alonso states, “The can body 12 of the outer can, the body 66 of the inner container 62 and the top wall 22 of the compartment 18 defines the vacuumized chambers 76 in which is located the refrigerant valve device 32 and which is normally free of air thereby providing a vacuum state.” The use of a vacuum is prohibitive in the commercialization of a self-cooling container. It is expensive to implement and can leak in a carbonated environment. Further as will be described further, it is not the effective to store a vacuum to achieve the desired results. Other patents that use endothermic cooling means include, U.S. Pat. Nos. 4,773,389, 3,561,424, 3,950,158, 3,887,346, 3,874,504, 4,753,085, 4,528,218, 5,626,022, and numerous others use endothermic reactions remove heat from water to cool the beverage food product container. These prior art technologies require two containers that may be connected by a breakable membrane and other means. They particularly do not permit the sorption of the humidification liquid to be achieved by automatic vacuum generation within the chemical chamber to permit complete solvation and complete use of the maximum surface area available.
For example, as stated earlier, Shotaro Sato of Osaka, Japan reveals an endothermic cooling process and apparatus in U.S. Pat. No. 3,970,068. Sato depends on using a valve system that is pushed by a finger from the outside of the beverage container so that the bottom cover pushes a needle existing between the compartments accommodating the exothermal or endothermal reaction agent and the reaction-inducing agent respectively, and to permit the two agents mix to produce thermal reaction as the result. The use of these specialized valves are common in most of the patents that involve endothermic reactants. Further, Sato uses a mechanism that requires sophisticated manufacturing processes with rigid non-flexible containers resulting in cost prohibitive manufacturing technics.
As stated earlier, Scudder, et al. reveal another version of an endothermic cooling device in U.S. Pat. No. 5,626,022. Scudder reveals a container for holding a material, such as a food, beverage or medicine, includes a cap and a container body. The container body has a material cavity unitarily formed with a reactant cavity. The reactant cavity contains a solid reactant, and the cap contains a liquid reactant that, when mixed, produce an endothermic or exothermic reaction, depending upon the reactants selected. The cap has a tubular body section with an actuator disc closing one end and a breakable barrier closing the other end. With the exception of the barrier, the cap is of unitary construction. The cap has one or more prongs extending from the inner surface of the disc toward the barrier. When a user depresses the actuator disc, it flexes inwardly and moves the prongs toward the barrier. The reactants mix when the prongs puncture the barrier. Heat transferred between the two cavities heats or cools the material. The wall of the container that defines the reactant cavity may be pleated or corrugated to promote heat transfer. Again, this inventor respectfully reveals a method of manufacture that is cost prohibitive and inefficient for endothermic cooling.
In U.S. Pat. No. 4,753,085, Bernard Labrousse L. P. E. of France reveals a single-use heat transfer packaging for drinks and foodstuffs which comprising a receptacle containing drink or food to be consumed, a thermal capsule being immersed at least partially into the drink or food, the said capsule having a portion which is deformable by pressure or by traction, triggering an exothermal or endothermal chemical reaction. In Labrousse's patent, pressure is used to trigger the cooling by actuating a valve that separates the reactants. He states on line 67, page 4, “By pressure on the deformable wall 27 directly or through a push member or perforator, the deformation can be transmitted to the capsule 25 by means of a push member, a screw or a key. In contrast to the embodiments shown in
The present invention differs from all the mentioned prior art and provides a novel cost effective and thermodynamically simple and viable means for cooling a beverage in a food product container by using the cooling potential of fixed amounts of reactants using electromotive force of a dry gas acting on a humidification liquid of suitable choice to achieve advantageous cooling of a beverage. Many trials and designs have been made to obtain the present configuration of the disclosed invention.
U.S. Pat. No. 10,018,395 to Darlene S. Boyd issued Jul. 10, 2018 also illustrates an endothermic cooling system. However, the use of dry gas is not revealed and again a rupturable-membrane is disclosed. In Boyd's disclosure she states on line 2, page 4, “The first chamber 16 and the second chamber 18 are separated by a barrier 24 that prevents the cooling agent from contacting the activating agent prior to activation of the beverage cooling device. The barrier 24 is further configured to be ruptured upon activation of the beverage cooling device such that the cooling agent and the activating agent come into contact with and react with each other in an endothermic reaction.”
The problem Boyd has in implementing the invention is that if the mere flexing of the barrier can force the vessel to change its shape and rupture the barrier, then it is able to rupture the walls of the barrier as well. She reveals on line 51, page 4, “The second chamber 38 is within the first chamber 36, and the barrier 34 surrounds the second chamber 38. In this manner, the barrier 38 forms a second chamber housing. As discussed above, the beverage cooling device 30 may be activated by flexing or squeezing the housing 32 such that the barrier 34 ruptures and releases the activating agent 42 to contact the cooling agent 40.” It is obvious that the invention does not teach how to activate the apparatus just using the opening means of the beverage container, but instead reveals that the apparatus that must be sterile and internal to the beverage container is “activated by flexing or squeezing the housing 32 . . . ”. Further, no other invention thus far revealed has demonstrated the features and advantages that are revealed in the present invention. The foregoing summarizes some of the special advantages of the present invention over prior art.
It is thus an objective of the present invention to provide a method of cooling a food product container using a novel simple means to remove heat from a food product using dry gas.
It is another objective of the present invention to provide a method of assembling the self-cooling a food product container in its completed form with a food product such as a beverage therein with a dry gas absorption means to generate a vacuum for pulling humidification liquid into the a chamber with endothermic reactants and dry gas for an endothermic cooling of a food product container.
It is still another object of the present invention to provide a self-cooling apparatus for cooling a food product container using a conventional filled and sealed food product container in its completed form using simple materials such as a thin plastic bag to cool a food product.
It is a further object of the present invention to provide an apparatus that uses the humidification of a substantially dry gas to evaporate water from solutions of ionized chemical compounds to generate a vacuum for pulling humidification liquid to endothermically reacting chemical compounds without the need for special orientation.
It is a further object of the present invention to provide an apparatus that uses dry gas to evaporate a liquid to further cool by evaporation.
It is finally an object of the present invention to provide an apparatus that is thermodynamically simple, viable, and cost effective for removing heat from a food product and thereby cooling the same.
The present invention accomplishes the above-stated objectives, as well as others, as may be determined by a fair reading and interpretation of the entire specification.
The efficiency is in the direct transfer of the bond energies from broken humidification liquid molecules to the reformation energy of humidification liquid vapor as a vapor that is immediately transported away or absorbed by dry gas humidification and taken away. An example using water is shown in
A food product container is provided, including a food product container having a release port and a release port opening means. The food product container preferably is one of a metal can and a plastic bottle. A dry gas is provided preferably having a dew point temperature in relation to humidification liquid vapor below 10° F.
The present invention accomplishes the above-stated objectives, as well as others, as may be determined by a fair reading and interpretation of the entire specification.
Dry gas such as substantially dry air, substantially dry CO2, substantially dry Nitrogen, substantially dry Dimethyl ether, several other types of dehumidified gases such as Solstice® L41y (R-452B), Solstice® 452A (R-452A), Solstice® L40X (R-455A), Solstice® zd, Solstice® ze, (R-1234ze), Solstice® yf (R-1234y) with very low dew point temperatures can cause extreme cooling.
Dry air in particular can cause extreme cooling as is evidenced by weather patterns that are predominantly driven by the humidity of air and heat energy available in the atmosphere. Not surprisingly, dry air can result in dramatic snow and ice formation, in turn resulting in extreme weather patterns across the world. It is not surprising that lip-balm used for dry lips sells well in winter. From hurricanes to tornadoes, to heavy snow storms, and icy winter storms, nature has provided an amazing electromotive heat transport means that can be emulated to assist in cooling a beverage and a food product using humidification and dehumidification of air. It is my theory that the tremendous vacuous energies of a tornado are a result of the sudden condensation of water vapor from the dehumidification of humidified dry air. Water vapor is 1840 times the volume of the same weight of liquid water, and so when a huge cloud condenses, a tremendous reduction in volume is obtained resulting a vacuum which appears as a funnel cloud of a tornado. No simple wind motion can generate such tremendous energies. Similarly, the humidification of very dry air results in very cold temperatures that results in snow storms. This happens as moisture is picked up by dry air and evaporated to remove heat from the surrounding environment followed by saturation of the same wet air which again deposits its vapor as moisture in as snow and hail.
Water has the best thermodynamic potential to cool a food product. It has the highest heat of evaporation and as such it can be used in combination with electromotive drying and regenerative processes that also rely on water molecules to cool a food product container. However, water does not easily evaporate due its high heat of evaporation and as such it must be “enticed” to do so by an appropriate means. Further, as water cools, for example in an endothermic reaction, and in a desiccant evaporation system, it becomes more and more difficult to evaporate it. Thus, neither endothermic cooling nor conventional desiccant cooling systems of prior art by themselves prove to be the most efficient forms of cooling a food product such as beverage. The combination of dry gas mediation, and other cooling methods can use the two fundamental substances, water and a dry gas, to effectively increase the thermodynamic potential to cool a food product. However, an inventive step of causing vacuums generated by the interaction of dry gases and a humidification liquid to maximize the cooling surface area of the apparatus is intended. Further, the additional inventive step of using flexible containers for the humidification liquid and the reactive chemicals such that a dry gas when interacted with the humidification liquid causes a vacuum that then minimizes and collapses the volume of the containment structures used for the invention is intended. Further, the additional inventive step of using the solvation of chemicals to generate a vacuum for the purposes of minimizing the volume of the containment structures used for the invention is intended.
The following definitions are generally used to describe some terms used in the present disclosure to describe this invention.
“Food product container” for the purposes of this application shall mean a food product container either made from metal or made from plastic and containing a food or beverage product as used by the invention.
“Food product” for the purposes of this application shall mean any substance that is a consumable item preferably a liquid beverage;
“Dew point temperature” for the purposes of this application shall mean the temperature at which the vapor of a humidification liquid in a sample of dry gas at constant barometric pressure condenses into humidification liquid at the same rate at which it evaporates.
“Headspace” for the purposes of this application shall mean the carbonation filled space in a sealed beverage container that is above the beverage level.
“Dry gas” for the purposes of this application, shall mean a gas with a substantially low partial water vapor pressure with a dew point temperature less than 50° F. that fills interstitial spaces between particles of endothermically reacting compounds. It is noted that the dry gas itself could be liquefied and mixed in with said endothermically reacting compounds;
“Wet gas” for the purposes of this application, shall mean a dry gas humidified to have a higher water vapor pressure than dry gas and a dew point temperature greater than 10° F.
“Heat transport means” for the purposes of this application, shall mean a thermodynamic and electromotive potential to exchange heat between substances;
“Compressible plug member” for the purposes of this application shall mean any structure made from materials such as a wax, a rubber, a plastic or a metal used to form a pressure activated valve in the form of a sealing plug to temporarily seal a cross-sectional area exposed to a fluid and preventing said fluid from passing through said cross-sectional area and such that said material can be compressed by pressure to a smaller cross-sectional area in a sealing configuration and such that upon release of said pressure, said material remains with smaller cross-sectional area.
“Interconnection structure” for the purposes of this application, shall mean a segment of the walls of a cooling assembly that is between a dry gas chamber and humidification liquid chamber.
“Collapsible” for the purposes of this application shall mean the reduction in volume of a closed space without a change in the surface area of the walls enclosing said volume.
“Pressure activated valve” for the purposes of this application shall mean a deformable and compressible plug member sealing inside the walls of a compressible interconnection structure and forming a non-permanent barrier between a humidification liquid chamber and a dry gas chamber containing endothermically reacting chemical compounds such that when the compressible interconnection structure is compressed by pressure, its cross-sectional area reduces and compresses the pressure activated valve to a smaller cross-sectional area and remains in a sealing configuration with the said compressible interconnection structure, and when the pressure is removed around the compressible interconnection structure, at least partially expands back to its original shape leaving the pressure activated valve with its smaller cross-sectional area and forming a gap between said pressure activated valve and the compressible interconnection structure to open fluid communication between the humidification liquid and the dry gas chamber.
“Humidification liquid chamber” for the purposes of this application shall mean a space containing humidification liquid sealed by one or more pressure activated valves.
“Endothermically reacting chemical compound” for the purposes of this application shall mean any chemical solid, liquid or gaseous compounds that can react with water and solvents to cool endothermically and that can dissolve in humidification liquid such as water to form ions from its elements or a combination of its elements thereof and cool endothermically.
“Humidification liquid” for the purposes of this application shall mean any liquid that is used to react with endothermically reacting chemical compounds to generate endothermic cooling and such liquid may include water and beverage.
“Collapsible volume” for the purposes of this application shall mean a closed structure having an internal volume with enclosing structure walls that can be restructured by the force of a vacuum to reduce the overall enclosed volume, specific examples being the reduction of said enclosed volume by bending said walls, the reduction of said enclosed volume by telescoping said walls, the reduction in said enclosed volume by the relative sliding of sections of said walls.
Humidification liquid vapor” for the purposes of this application shall mean the vapor of any humidification liquid.
“Dry gas chamber” for the purposes of this application is a functional structure that preferably contains a dry gas and may hold endothermically reacting chemical compounds in the form of solids or liquids within it.
“PVC” for the purposes of this application shall mean heat-shrinkable polyvinyl chloride.
“PET” for the purposes of this application shall mean heat-shrinkable polyethylene tetraphthalate.
“Upright” for the purposes of this application shall mean vertical orientation.
“Interconnection structure” for the purposes of this application shall mean a wall portion of a cooling assembly wall that abuts and sealing surrounds a compressible plug member.
For orientation purposes and clarity, the food product container is assumed to be standing in an upright, vertical orientation with the food product container's bottom resting on a horizontal plane.
This invention uses the thermodynamic potential of the evaporation of a humidification liquid such as water, water-ethanol azeotropes, dimethyl ether-water azeotropes, or a suitable liquid and the ability of a substantially low vapor pressure medium such as a dry gas to force this evaporation from even cold liquids. To do this, a standard food product container such as a can or a bottle is provided. “Food product container” is preferably a cylindrical beverage food product container of standard design, and with standard food product release means and a standard food product release port.
Method of Manufacture of the First Embodiment of the Present Invention
In the first embodiment, shown in
Thus, a humidification liquid chamber, and a dry gas chamber, with an interconnection structure between the two, are provided in the form of a flexible and collapsible structure such as a bag formed with thin bag material preferably in the form of lay-flat plastic bags with a metallized lining. By collapsible is meant that the shape and volume contained within the flexible humidification liquid chamber walls can change as a result of pressure changes.
As shown in
The interconnection structure is provided. The interconnection structure is made from a preferably a ½″ to ¾″ silicone tube that is about 1″ long. The interconnection structure is therefore deformable and compressible when a force is applied to its walls but can to go back to its original shape when the deforming force is removed. The interconnection structure is first placed inside the lay-flat tubing with is axis parallel to the axis of the expanded lay-flat tubing. It is positioned centrally along the length of the lay-flat so that its length and width project symmetrically from the center point of the lay-flat tubing. Then a heat sealer is used to seal across the center of the lay-flat tubing to forms seal that divides the length of the lay-flat tubing into two equal portions with open ends. The interconnection structure in this case will not be affected by the heat sealing of the lay-flat tubing since the melt temperature of silicone material is far higher that the melt temperature of the lay-flat tubing. However, the interconnection structure will be trapped in the center of the lay-flat tubing to form a tubular fluid connecting structure between the two halves of the lay-flat tubing.
As shown in
If the bag material used to form the cooling assembly is too thin, a supporting flexible silicone rubber tube may be added to line the inside walls of the interconnection structure to permit the interconnection structure to be compressed to a smaller cross-sectional area by pressure acting around its outer surface, and to permit its walls to bounce back to the original shape when the pressure is released. Thus the interconnection structure may be made as a separate segment a thin-walled flexible tube. The interconnection structure may also be made from a one of a silicone rubber material and a plastic material to permit its walls to be compressed by external pressure to a smaller cross-section and yet also permit it to bounce back to its original shape when the compressing pressure is released and alternatively, it may be made as mentioned above from thin bag material that is reinforced by one of a rubber tube and a plastic tube to permit it to bounce back to its original shape when deformed by pressure. It may also be made from an elastic plastic that can be compressed by pressure and that will bounce back to its original shape when the pressure is released.
The next step in making the apparatus is to fill the inside of the interconnection structure with a compressible plug member to serve as a pressure activated valve for the apparatus between the humidification liquid chamber and the dry gas chamber. The compressible plug member which serves as a pressure activated valve, is preferably made from a suitable deformable material, one of non-resilient and only partially resilient material such as a non-water-soluble wax, a rubber, a plastic, cork, closed foam, and a non-soluble putty. The compressible plug member is placed to sealingly plug and seal either a portion or the entire interconnection structure to sealingly separate the dry gas chamber from the humidification liquid chamber. The compressible plug member can also be made as a deformable metal or plastic disc that snugly fits the circumferential diameter of the inside of the interconnection structure to act as a barrier between the humidification liquid chamber and the dry gas chamber. As shown in
The next step in manufacturing the apparatus is filling the dry gas chamber with granular forms of the endothermically reacting chemical compounds through its open unsealed end. The endothermically reacting chemical compounds should be made to fill and contact the maximum possible surface area of the dry gas chamber walls. Of course while the surface area of the dry gas chamber is fixed by the lay-flat tubing material area available to form the dry gas chamber, however, the volume of the dry gas chamber depends on the extent to which the lay-flat tubing that forms the dry gas chamber is expanded. Advantageously any volume between the maximum expanded volume and the minimum lay-flat volume of the two chambers can be accommodated in the same surface area of the dry gas chamber.
The next step is to flood the dry gas chamber with a dry gas, preferably one of dry CO2, dry dimethyl ether (DME), and one or combinations of DME, CO2, Solstice® L41 y (R-452B), Solstice® 452A (R-452A), Solstice® L40X (R-455A), Solstice® zd, Solstice® ze, (R-1234ze), Solstice® yf (R-1234yf). The dry gas is filled by simply blowing it at a low flow rate through the granules of the endothermically reacting chemical compounds to replace any air that fills the interstitial spaces between the granules of the endothermically reacting chemical compounds. The next step is to thermally seal the dry gas chamber by heat sealing the open end of the dry gas chamber to form a closed dry gas chamber.
The next step in the assembly of the apparatus is to fill the humidification liquid chamber with humidification liquid. The humidification liquid must be chosen to react endothermically with the endothermically reacting chemical compounds and to also evaporate when subjected to the dry gas. Preferably, the humidification liquid is water. The humidification liquid should contact the maximum possible surface area of the humidification liquid chamber that is available. Of course while the surface area of the dry gas chamber is fixed by the lay-flat tubing material, the volume of the humidification liquid chamber depends on the extent to which the lay-flat tubing that forms the humidification liquid chamber can be expanded. Advantageously any volume between the maximum expanded volume and the minimum lay-flat volume of the two chambers can be accommodated. The next step is to thermally seal the humidification liquid chamber by heat sealing the open end of the humidification liquid chamber to form a closed humidification liquid chamber.
A standard beverage container is provided preferably in the form of a conventional metal can or in the form of a plastic bottle. The cooling assembly comprising the humidification liquid chamber, the dry gas chamber and the interconnection structure with the compressible plug member separating the two chambers is then inserted into the beverage container. Carbonated beverage is then filled into the beverage container by conventional means. A beverage container lid with a beverage container opening means is provided for closing the container and thereby sealing off the beverage with the cooling assembly to form the apparatus according to the first embodiment.
For a can, the beverage container opening means is also conventionally referred to as the “pull tab”. However, in the case when the beverage container is a plastic bottle, the container opening means is a beverage container lid in the form of a conventional screw-on cap that seals a threaded neck portion of the bottle and also acts as the beverage opening means. When the beverage container is sealed off by the beverage container lid, carbonation pressure builds up. The carbonation pressure of the beverage compresses the humidification liquid chamber and the dry gas chamber and the interconnection structure until the internal pressure of the humidification liquid chamber and the dry gas chamber equals the carbonation pressure. The carbonation pressure also deforms the interconnection structure and compresses the interconnection structure and the compressible plug member to a smaller cross-sectional area than the starting cross-sectional areas while the compressible plug member still remains in a sealing configuration. The apparatus is now ready for use.
Upon opening the beverage container opening means, the change in internal pressure from loss of carbonation gases to atmosphere causes the interconnection structure to expand to its original state leaving the compressed compressible plug member at the smaller cross-sectional area. The difference in dimensions between the final compressed state of the compressible plug member and the starting uncompressed state of the compressible plug member forms a gap between the compressible plug member and the interconnection structure that permits fluid communication between the dry gas chamber and the humidification liquid chamber. The stages of compression and area reductions are shown in
A second embodiment of the invention is shown in
In one preferred method of manufacture of the second embodiment, a humidification liquid chamber, a dry gas chamber and an interconnection structure are provided in the form of an injection-stretch-blown thin-walled container. A preform is made and stretch-blown to form the cooling assembly and take the shape of a bottle that forms the dry gas chamber, and to form an interconnection structure as a narrow neck connecting to a bellows-shaped chamber that forms the humidification liquid chamber as shown in
The first step in forming a cooling assembly of the invention is to prepare a preform to form the two chambers and the interconnection structure as a single or multiple stretch-blown plastic pieces, preferably as a thin-walled structure, with flexible walls. The humidification liquid chamber is preferably a bellows-shaped structure while the dry gas chamber is preferably a cylindrically shaped structure, and the interconnection structure is preferably a small tube connecting the two chambers respectively. Preferably a plastic material such as one of PET, PVC, Polyethylene, and Polycarbonate, is used for this example. Preferably, the material used is made from substantially impervious film materials that prevent to a great extent beverage and carbonation from passing through its walls. If made as a single blown piece, a blow spout is provided and this blow spout can serve to fill the dry gas chamber, the interconnection structure and the humidification liquid chamber with their respective ingredients.
The second step in the making of the cooling assembly of the apparatus is to fill the humidification liquid chamber (the bellows) with humidification liquid through the blow spout. The humidification liquid must be chosen to react endothermically with the endothermically reacting chemical compounds and to also evaporate when subjected to the dry gas. Preferably, the humidification liquid is water. Of course while the surface area of the dry gas chamber is preferably substantially fixed as a cylinder, the volume of the bellows of the humidification liquid chamber depends on the extent to which its bellows shape can be expanded and contracted. Advantageously any volume between the maximum expanded volume of the bellows of the humidification liquid chamber and the minimum possible contracted volume of the bellows of the humidification liquid chamber can be accommodated.
The third step in making a cooling assembly according to the second embodiment of the invention is to fill the interconnection structure between the humidification liquid chamber and the dry gas chamber with a compressible plug member. The compressible plug member is preferably made from a suitable deformable structure made of one of non-resilient and only partially resilient material such as a non-water-soluble wax, a thin metal, a rubber, a plastic, cork, closed foam, or a putty. The compressible plug member is passed through the blow spout and placed to sealingly fill either a portion or the entire interconnection structure to separate the dry gas chamber from the humidification liquid chamber. The compressible plug member can also be made as a deformable metal disc and as a deformable metal cylinder such that it irreversibly deforms in cross-sectional area under pressure. Thus the compressible plug member material fluidly seals and separates the humidification liquid chamber from the dry gas chamber. The interconnection structure sealingly connects to the dry gas chamber and to the humidification liquid chamber. The compressible plug member, if made from a wax, can be simply melted and poured to substantially fill the interconnection structure. Since a wax floats on water for example, it is possible to fill the water in the humidification liquid chamber up to the start of the interconnection structure and then pour molten wax to float above the humidification liquid and fill the interconnection structure.
The fourth step in manufacturing the apparatus according to the second embodiment is filling the dry gas chamber with granular forms of the endothermically reacting chemical compounds through its open unsealed end. The endothermically reacting chemical compounds should be made to fill and contact the maximum possible surface area of the dry gas chamber walls.
The fifth step in manufacturing the apparatus according to the second embodiment is to flood the dry gas chamber with a substantially dry gas, preferably one of CO2, dimethyl ether (DME), and one or combinations of substantially dry gases such as DME, CO2, Solstice® L41 y (R-452B), Solstice® 452A (R-452A), Solstice® L40X (R-455A), Solstice® zd, Solstice® ze, (R-1234ze), Solstice® yf (R-1234y). The dry gas is filled by simply blowing it at a low flow rate through the granules of the endothermically reacting chemical compounds to replace any air that fills the interstitial spaces between the granules of the endothermically reacting chemical compounds. The next step is to thermally seal the dry gas chamber by heat sealing the open end of the blow spout to form a closed dry gas chamber and to form the completed cooling assembly shown in
A standard beverage container is provided in the form of a conventional metal can or in the form of a plastic bottle. The cooling assembly comprising the humidification liquid chamber, the dry gas chamber contents and the interconnection structure with the compressible plug member separating the two is then inserted into the beverage container. Carbonated beverage is then filled into the beverage container by conventional means. A beverage container lid with a beverage container opening means is provided for sealing off the beverage with the cooling assembly to form the apparatus according to the first embodiment.
When the beverage container is closed and sealed by the beverage container lid, carbonation pressure builds up within the container and around the cooling assembly. The carbonation pressure of the beverage compresses the humidification liquid chamber and the dry gas chamber and the interconnection structure until the internal pressure of the humidification liquid chamber and the dry gas chamber equals the carbonation pressure. The carbonation pressure also deforms and compresses the interconnection structure and the compressible plug member within the interconnection structure to smaller cross-sectional areas than the starting cross-sectional area while the compressible plug member maintains a sealing configuration. The apparatus is now ready for use.
Upon opening the beverage container opening means, the change in carbonation pressure causes the interconnection structure to expand at least to some extent and preferably to its original state leaving the compressed compressible plug member at the smaller cross-sectional area. The difference in dimensions between the final compressed state of the compressible plug member and the starting uncompressed state of the compressible plug member must form a gap that permits fluid communication between the dry gas chamber and the humidification liquid chamber. The stages of compression and area reductions are shown in
A third embodiment of the invention is shown in
In the third embodiment of the invention, the same elements used in the first embodiment are used to reconfigure another embodiment of the invention that uses telescoping cylindrical chambers instead of collapsible flexible-walled chambers to form a collapsible volume system. A standard beverage container is provided with a beverage lid and a beverage opening means containing a beverage that is carbonated and under pressure. The beverage container may be a metal can of standard conventional form or a plastic bottle of conventional form. The humidification liquid chamber and the dry gas chamber are provided within the sealed beverage container as described hereunder.
A thin cylindrical-walled humidification liquid chamber is provided. The humidification liquid chamber is configured as a cylindrical cup in the form of a tubular cup side wall terminating in a cup end wall and an opposing cup open end. Humidification liquid such as water is held within the humidification liquid chamber and a compressible plug member made from preferably a suitable deformable material which is one of non-resilient and only partially resilient, examples of which include deformable waxes, metals, rubbers and plastics, placed to seal off the humidification liquid chamber or the dry gas chamber, and fluidly isolate the humidification liquid chamber. This easily can be achieved by filling the humidification liquid chamber with water for example, heating the water, and melting a suitable wax over the water to form a wax seal layer. When the wax dries, it forms a hermetic seal over the humidification liquid and seals off the open end of the humidification liquid chamber.
Similarly, a dry gas chamber is provided comprising thin a cylindrical-walled container with an open end. The dry gas chamber contains crystalline forms of endothermically reacting chemical compounds such as potassium nitrate, potassium chloride and urea. Dry gas is flowed into the dry gas chamber to fill the interstitial spaces between the crystals of the endothermically reacting chemical compounds. When the humidification liquid chamber is slid telescopically into the dry gas chamber, the interconnection structure is placed over the assembly to hold the two chambers in place and to snugly and frictionally and sealingly connect them and to prevent them from sliding apart.
It is also important that the dry gas be chilled to a temperature that prevents fast pressure build up that can separate the two chambers before the beverage container is sealed off with the beverage container lid. The internal pressure of the dry gas will build up until it equilibrates with the beverage carbonation pressure. As such, the pressure of the dry gas as it heats up to room temperature and gasifies cannot exceed the carbonation pressure. The carbonation pressure compresses the interconnection structure and this compresses the compressible plug member to a smaller diameter than its starting diameter while in a sealing configuration.
The interconnection structure is preferably made in the form of one of a plastic sleeve and a rubber sleeve to tightly and slidingly connect to and to seal off the open ends of the dry gas chamber and the humidification liquid chamber. The open end of the dry gas chamber preferably is made to snugly and sealingly slide over the plugged end of the humidification liquid chamber. Thus when the humidification liquid chamber is sealingly slid into the dry gas chamber, the reduced combined volume of the two chambers will preferably be made to equal to the volume of the dry gas chamber only. The entire cooling assembly can be left to just float inside the beverage container in the beverage, and alternatively the cooling assembly may also be affixed to the beverage container inner wall at any place or orientation.
When the beverage container is filled and sealed off as before by the beverage container lid, carbonation pressure builds up internally within the beverage container. The carbonation pressure compresses the interconnection structure and causes the dry gas chamber wall and the humidification liquid chamber wall to compress around the compressible plug member until the internal pressure of the humidification liquid chamber and the dry gas chamber equals the carbonation pressure. The cross-sectional area of the compressible plug member reduces due to carbonation pressure compression.
Upon opening the beverage container opening means, the change in carbonation pressure causes the interconnection structure to relax its pressure compression that is transmitted to the compressible plug member. The compressible plug member remains in a deformed smaller cross-section and the difference in dimensions between the final compressed state of the compressible plug member and the starting uncompressed state of the compressible plug member permits fluid communication between the dry gas chamber and the humidification liquid chamber, and the dry gas starts to absorb humidification liquid, forming a vacuum and pulling humidification liquid into the dry gas chamber. The humidification liquid chamber is pulled further into the dry gas chamber by the generated vacuum. Some humidification liquid vapor is evaporated during this process as well. The endothermically reacting chemical compounds react with the humidification liquid and dissolve endothermically to cool the beverage product. The solvation causes a further reduction in volume of the dry gas chamber and this causes more humidification liquid and humidification liquid vapor to be pulled into the dry gas chamber. Thus a complete dissolving of the endothermically reacting chemical compounds occurs and cooling of the beverage product occurs. It is important that the surface areas of the humidification liquid chamber and the dry gas chamber be respectively maximized for best cooling.
Various other objects, advantages, and features of the invention will become apparent to those skilled in the art from the following discussion taken in conjunction with the following drawings representing the preferred embodiments of the invention, in which:
As required, detailed embodiments of the present invention are disclosed herein; however, it is to be understood that the disclosed embodiments are merely exemplary of the invention which may be embodied in various forms. Therefore, specific structural and functional details disclosed herein are not to be interpreted as limiting, but merely as a basis for the claims and as a representative basis for teaching one skilled in the art to variously employ the present invention in virtually any appropriately detailed structure.
Reference is now made to the drawings, wherein like characteristics and features of the present invention shown in the various FIGURES are designated by the same reference numerals.
For orientation purposes and clarity, the food product container is assumed to be standing in a vertical orientation and thus in its normal placement orientation. This invention uses the thermodynamic potential of the evaporation of a humidification liquid, such as water or other suitable liquid, and the ability of a substantially low vapor pressure medium such as a dry gas DG to force this evaporation from even cold liquids.
A first embodiment of the invention is shown in
In one preferred method of manufacture of the first embodiment, a humidification liquid chamber 104, a dry gas chamber 106 and the interconnection structure 107 are provided in the form of a contiguous flexible and collapsible structure such as a lay-flat tubing preferably in the form of metalized lay-flat tubing 105. A lay-flat-tube 105, preferably with an expanded diameter of about 2-3 inches and about 8-12 inches long, is first provided with open ends. In one embodiment as shown in
As shown in
As shown in
The next step in manufacturing the apparatus 10 is filling the dry gas chamber 106 with granular forms of the endothermically reacting chemical compounds R through its open unsealed end. The endothermically reacting chemical compounds R should be made to fill and contact the maximum possible surface area of the dry gas chamber walls 110. Of course, while the surface area of the dry gas chamber 106 is fixed by the lay-flat tubing 105 material area available to form the dry gas chamber 106, the volume of the dry gas chamber 106 depends on the extent to which the lay-flat tubing 105 that forms the dry gas chamber 106 is expanded. Advantageously any volume between the maximum expanded volume and the minimum lay-flat volume of the two chambers can be accommodated in the same surface area of the dry gas chamber 106.
A further step is making a cooling assembly 100 of the invention is to fill the interconnection structure 107 between the humidification liquid chamber 104 and the dry gas chamber 106 with a compressible plug member 108. The compressible plug member 108 is preferably made from a suitable deformable material, one of non-resilient and only partially resilient material such as a non-water-soluble wax, a rubber, cork, closed foam, a plastic, and a putty. In
The compressible plug member 108 is placed to sealingly fill either a portion or the entire interconnection structure 107 to separate the dry gas chamber 106 from the humidification liquid chamber 104. The compressible plug member 108 can also be made as one of a deformable metal and plastic disc such that the disc can irreversibly deform in cross-section when compressed by beverage pressure acting against the interconnection structure 107. Thus the compressible plug member 108 is made from materials that fluidly seal and separate the humidification liquid chamber 104 from the dry gas chamber 106. The interconnection structure 107 sealingly connects the dry gas chamber wall 110 to the humidification liquid chamber wall 109. Both the dry gas chamber 106 and the humidification liquid chamber 104 can also be made as separate bags connected sealingly to the ends of the interconnection structure 107 by means of thermal welding. As shown in
Alternatively, the narrowing of the lay-flat tubing 105 to form a narrow neck for a smaller interconnection structure 107 is only necessary if the amount of material used to form the compressible plug member 108 needs to be reduced to minimize its thermal penalty on the cooling capacity of the apparatus 10. The cooling assembly 100 may also be formed from a single unaltered tube material as shown in
If lay-flat tubing 105 material that is used to form the cooling assembly 100 is too thin, i.e., in the order of magnitude of thickness less than 1 mil, a supporting flexible rubber tube segment may be added to form the interconnection structure 107 to permit the interconnection structure 107 to be compressible by carbonation pressure P to a smaller cross-sectional area, and also to permit the interconnection structure 107 to bounce back to its original shape when the pressure is released, using the rubber material's elasticity. Thus, the interconnection structure 107 may be made as a separate segment of the cooling assembly 100 as shown in
The next step in manufacturing the apparatus 10 is filling the dry gas chamber 106 with granular particles of the endothermically reacting chemical compounds R through its open unsealed end. The endothermically reacting chemical compounds R should be made to fill and contact the maximum possible surface area of the dry gas chamber wall 109. Of course, while the surface area of the dry gas chamber wall 109 is fixed by the lay-flat tubing 105 material's available area, the volume of the dry gas chamber 106 depends on the extent to which the lay-flat tubing 105 forming the dry gas chamber 106 can be expanded. Advantageously, both the dry gas chamber 106 and the humidification liquid chamber 104 can have any volume between the maximum expanded cylindrical volume of lay-flat tubing 105, and the minimum lay-flat volume of lay-flat tubing 105, while both chambers maintain a constant surface area respectively.
The next step is to flood the dry gas chamber 106 with a dry gas DG, preferably one of dry CO2, dry dimethyl ether (DME), and one or combinations of DME, CO2, Solstice® L41y (R-452B), Solstice® 452A (R-452A), Solstice® L40X (R-455A), Solstice® zd, Solstice® ze, (R-1234ze), and Solstice® yf (R-1234y). The dry gas DG is filled by simply blowing it at a low flow rate through the granules of the endothermically reacting chemical compounds R to replace any air that fills the interstitial spaces between the granules of the endothermically reacting chemical compounds R. The next step is to thermally seal the dry gas chamber 106 by heat sealing the open end of the dry gas chamber 106 to form a sealed chamber.
If the amount of dry gas DG needed exceeds the pressure rating of the dry gas chamber 106, a simple remedy is shown in
The next step in the assembly of the apparatus 10 is to fill the humidification liquid chamber 104 with humidification liquid HL. The humidification liquid HL must be chosen to react endothermically with the endothermically reacting chemical compounds R and to also evaporate when subjected to the dry gas DG. Preferably, the humidification liquid HL is water. The humidification liquid HL should contact the maximum possible surface area of the humidification liquid chamber 104 that is available. Of course while the surface area of the dry gas chamber 106 is fixed by the lay-flat tubing 105 material, the volume of the humidification liquid chamber 104 depends on the extent to which the lay-flat tubing 105 that forms the humidification liquid chamber 104 can be expanded. Advantageously any volume between the maximum expanded volume and the minimum lay-flat volume of the two chambers can be accommodated. The next step is to thermally seal the humidification liquid chamber 104 by heat sealing its open end to form a closed humidification liquid chamber 104.
A standard beverage container 20 is provided in the form of a conventional metal can or in the form of a plastic bottle. The cooling assembly 100 comprising the humidification liquid chamber 104, the dry gas chamber 106 and chamber contents, and the interconnection structure 107 with the compressible plug member 108 separating the two, is then inserted into the beverage container 20. Carbonated beverage B is then filled into the beverage container 20 by conventional means. A beverage container lid 102 with a beverage container opening means 103 is provided for sealing off the beverage with the cooling assembly 100 to form the apparatus 10 according to the first embodiment.
When the beverage container 20 is sealed off by the beverage container lid 102, carbonation pressure P builds up. The carbonation pressure P of the beverage B compresses the humidification liquid chamber 104 and the dry gas chamber 106 and the interconnection structure 107 until the internal pressure of the humidification liquid chamber 104 and the dry gas chamber 106 equals the carbonation pressure P. The carbonation pressure P also deforms the interconnection structure 107 and compresses the interconnection structure 107 and the compressible plug member 108 to a smaller cross-sectional area than their starting cross-sectional areas while the compressible plug member 108 still remains in a sealing configuration. The apparatus 10 is now ready for use.
Upon opening the beverage container opening means 103, the change in the container 20's internal carbonation pressure P to atmospheric pressure, causes the interconnection structure 107 to substantially expand preferably back to its original state, leaving the compressed compressible plug member 108 at a smaller cross-sectional area. The difference in dimensions between the final compressed state of the compressible plug member 108 and the starting uncompressed state of the compressible plug member 108 forms a gap that permits fluid communication between the dry gas chamber 106 and the humidification liquid chamber 104. The stages of compression and area reductions are shown in
A second embodiment of the invention is shown in
The first step in forming a cooling assembly 100 of the present invention is to prepare a preform to form the two chambers and the interconnection structure 107 as a single or multiple stretch-blown plastic pieces, preferably as thin-walled structures with flexible walls. The humidification liquid chamber 104 is preferably a bellows-shaped structure, while the dry gas chamber 106 is preferably a cylindrically-shaped structure, and the interconnection structure 107 is preferably a small tube connecting the two chambers respectively. Preferably, a plastic material such as one of PET, PVC, Polyethylene, and Polycarbonate, is used for this example. The material used preferably is made from substantially impervious plastic materials that prevent to a great extent beverage and carbonation from passing through its walls.
The second step in the making of the cooling assembly 100 of the apparatus 10 is to fill the humidification liquid chamber 104 (the bellows) with humidification liquid HL through the blow spout 120. The humidification liquid HL must be chosen to react endothermically with the endothermically reacting chemical compounds R and to also evaporate when subjected to the dry gas DG. Preferably, the humidification liquid HL is water. Of course while the surface area of the dry gas chamber 106 is preferably substantially fixed as a cylinder, the volume of the humidification liquid chamber 104 depends on the extent to which its bellows shape can be expanded and contracted. Advantageously, any volume between the maximum expanded volume of the humidification liquid chamber 104 and the minimum possible contracted volume of the bellows can be accommodated.
The third step in making cooling assembly 100, according to the second embodiment of the invention, is to fill the interconnection structure 107 between the humidification liquid chamber 104 and the dry gas chamber 106 with a compressible plug member 108. The compressible plug member 108 is preferably made from a suitable deformable material, one of non-resilient and only partially resilient material such as a non-water-soluble wax, a rubber, cork, closed foam, a plastic, and a putty. The compressible plug member 108 is passed through the blow spout 120 and placed to sealingly fill either a portion or the entire interconnection structure 107 to separate the dry gas chamber 106 from the humidification liquid chamber 104. The compressible plug member 108 also can be made as a deformable metal disc and as a deformable metal cylinder such that it irreversibly or only partially reversibly deforms in cross-sectional area under beverage carbonation pressure, P. Thus, the compressible plug member 108 fluidly seals and separates the humidification liquid chamber 104 from the dry gas chamber 106. The interconnection structure 107 sealingly connects to the dry gas chamber 106 and to the humidification liquid chamber 104. The compressible plug member 108, if made from a wax, can be simply melted and poured to fill the interconnection structure 107. Since a wax floats on water, for example, it is possible to fill the water in the humidification liquid chamber 104 up to the start of the interconnection structure 107 and then pour molten wax to float above the humidification liquid HL and fill the interconnection structure 107.
The next step in manufacturing the apparatus 10 according to the second embodiment is filling the dry gas chamber 106 with granular forms of the endothermically reacting chemical compounds R through its open unsealed blow spout 120. The endothermically reacting chemical compounds R should be made to fill and contact the maximum possible surface area of the dry gas chamber walls 109.
The next step is to flood the dry gas chamber 106 through the blow spout 120, with a substantially dry gas DG, preferably one of CO2, dimethyl ether (DME), and one or combinations of DME, CO2, Solstice® L41 y (R-452B), Solstice® 452A (R-452A), Solstice® L40X (R-455A), Solstice® zd, Solstice® ze, (R-1234ze), and Solstice® yf (R-1234yf). The dry gas DG is filled by simply blowing it at a low flow rate through blow spout 120 into the granules of the endothermically reacting chemical compounds R to replace any air that fills the interstitial spaces between the granules of the endothermically reacting chemical compounds R. The next step is to thermally seal the dry gas chamber 106 by heat sealing the open end of the blow spout 120 to form a closed dry gas chamber 106 and to form the completed cooling assembly 100, as shown in
A standard beverage container 20 preferably is provided in the form of a conventional metal can or in the form of a plastic bottle. The cooling assembly 100, comprising the humidification liquid chamber 104, the dry gas chamber 106 and the interconnection structure 107 with the compressible plug member 108 separating the two, is then inserted into the beverage container 20. Carbonated beverage B is then filled into the beverage container 20 by conventional means. A beverage container lid 102 with a beverage container opening means 103 is provided for sealing off the beverage container 20 with the cooling assembly 100 inside to form the apparatus 10 according to the second embodiment.
When the beverage container 20 is sealed off by the beverage container lid 102, carbonation pressure P builds up. The carbonation pressure P of the beverage compresses the humidification liquid chamber 104 and the dry gas chamber 106 and the interconnection structure 107 until the internal pressure of the humidification liquid chamber 104 and the internal pressure dry gas chamber 106 and the internal pressure of the interconnection structure equal the carbonation pressure P. The carbonation pressure P also deforms the interconnection structure 107 and compresses the interconnection structure 107 and the compressible plug member 108 to a substantially smaller cross-sectional area than its starting cross-sectional area, while the compressible plug member 108 still remains in a sealing configuration. The apparatus 10 is now ready for use.
Upon opening the beverage container opening means 103, the change in internal pressure within the beverage container 20, from carbonation pressure P to atmospheric pressure Pa, causes the interconnection structure 107 to substantially expand back preferably to its cross-sectional area, leaving the compressed compressible plug member 108 at the smaller cross-sectional area than the expanded cross-sectional area of the interconnection structure 107. The difference in dimensions between the final compressed state of the compressible plug member 108 and the starting uncompressed state of the compressible plug member 108 forms a gap that permits fluid communication between the dry gas chamber 106 and the humidification liquid chamber 104. The stages of compression and area reductions are shown in
A third embodiment of the invention is shown in
A thin cylindrical-walled humidification liquid chamber 104 is provided. Humidification liquid chamber 104 is configured as a cylindrical cup with a tubular cup side wall 104c with a cup open end 104a and a cup end wall 104b opposing the cup open end 104a. Humidification liquid HL such as water is held within the humidification liquid chamber 104 and a compressible plug member 108 preferably made from a suitable irreversibly deformable material which is one of non-resilient and only partially resilient material such as deformable wax, rubber, and plastic, is placed to seal off the humidification liquid chamber 104 open end and fluidly isolate the humidification liquid chamber 104. This can easily be achieved by filling the humidification liquid chamber 104 with water for example, heating the water, and melting a suitable wax over the water surface to form a wax sealing layer. When the wax dries, it forms a hermetic seal over the humidification liquid HL and seals off the open end of the humidification liquid chamber 104.
Similarly, a dry gas chamber 106 is provided comprising a thin cylindrical-walled container having a tubular cup side wall 106c with a cup open end 106a and a cup end wall 106b opposing the cup open end 106a. The dry gas chamber 106 contains crystalline forms of endothermically reacting chemical compounds R such as potassium nitrate, potassium chloride and urea. Dry gas DG is flowed into the dry gas chamber 106 to fill the interstitial spaces between the crystals of the endothermically reacting chemical compounds R. When the humidification chamber 104 is slid into the dry gas chamber 106, the interconnection structure 107 is placed over the assembly not only to hold the two chambers in place and to snugly and frictionally and sealingly connect them but also to prevent them from sliding apart. Alternatively, compressible plug member 108 may be filled into the interconnection structure 107 to abut and seal against the interconnection structure 107, to separate the dry gas chamber 106 and the humidification liquid chamber 104.
It is also important that the dry gas DG be chilled to a temperature to prevent fast pressure build up that can drive apart and separate the two chambers before the beverage container 20 is sealed off with the beverage container lid 102. The internal pressure of the dry gas DG will build up until it also equilibrates with the beverage carbonation pressure P. As such, the pressure of the dry gas DG as it heats up to room temperature and gasifies cannot exceed the carbonation pressure P. The carbonation pressure P compresses the interconnection structure 107, and this compresses the compressible plug member 108 to a smaller diameter than its starting diameter while remaining in a sealing configuration.
The interconnection structure 107 preferably is made in the form of one of a plastic sleeve and a rubber sleeve, to tightly and slidingly seal off the open ends of the dry gas chamber 106 and the humidification liquid chamber 104. The dry gas chamber open end 106a is made to snugly and sealingly slide over the side wall and the end wall of the humidification liquid chamber wall 110. Thus, when the humidification liquid chamber 104 is sealingly slid into the dry gas chamber 106, the reduced combined volume of the two chambers will substantially and preferably be made to equal to the volume of the dry gas chamber 106 only. The entire cooling assembly 100 can be left to just float inside the beverage container 20 in the beverage B, and alternatively the cooling assembly 100 also may be affixed to the beverage container inner wall 20a at any place or orientation.
When the beverage container 20 is filled and sealed off as before by the beverage container lid 102, carbonation pressure P builds up internally within the beverage container 20. The carbonation pressure P compresses the interconnection structure 107, which compresses around the compressible plug member 108 until the internal pressure of the humidification liquid chamber 104 and the dry gas chamber 106 equals the carbonation pressure P. The cross-sectional area of the compressible plug member 108 in turn reduces due to carbonation pressure P compression.
Upon opening the beverage container opening means 103, the change in container 20's internal carbonation pressure P to atmospheric pressure Pa, causes the interconnection structure 107 to relax its pressure compression grip that is transmitted to the compressible plug member 108. The compressible plug member 108 remains in a deformed smaller cross-section and the difference in dimensions between the final compressed state of the compressible plug member 108 and the uncompressed state of the compressible plug member 108 permits fluid communication between the dry gas chamber 106 and the humidification liquid chamber 104, and the and the dry gas DG starts to absorb humidification liquid HL forming a vacuum V and pulling humidification liquid HL into the dry gas chamber 106. The humidification liquid chamber 104 is pulled further into the dry gas chamber 106 by the generated vacuum. Some humidification liquid HL vapor is evaporated during this process as well. The endothermically reacting chemical compounds R react with the humidification liquid HL and dissolve endothermically to cool the beverage B. The solvation causes a further reduction in volume of the dry gas chamber 106 and this causes more humidification liquid HL and humidification liquid vapor to be pulled into the dry gas chamber 106. Thus a complete dissolving of the endothermically reacting chemical compounds R occurs and cooling of the beverage B occurs. It is important that the surface areas of the humidification liquid chamber 104 and dry gas chamber 106 be maximized for best cooling.
While the invention has been described, disclosed, illustrated and shown in various terms or certain embodiments or modifications which it has assumed in practice, the scope of the invention is not intended to be, nor should it be deemed to be, limited thereby and such other modifications or embodiments as may be suggested by the teachings herein are particularly reserved especially as they fall within the breadth and scope of the claims here appended.
This application is a continuation-in-part of application Ser. No. 15/932,812 filed on Apr. 30, 2018, which is a divisional of application Ser. No. 14/120,540, filed on May 30, 2014.
Number | Name | Date | Kind |
---|---|---|---|
2300793 | Martin | Nov 1942 | A |
3229478 | Alonso | Jan 1966 | A |
3494143 | Barnett et al. | Feb 1970 | A |
3970068 | Sato | Jul 1976 | A |
4584848 | Barnett | Apr 1986 | A |
4669273 | Fischer et al. | Jun 1987 | A |
4688395 | Holcomb | Aug 1987 | A |
4753085 | Labrousse | Jun 1988 | A |
4928495 | Siegel | May 1990 | A |
4993237 | Bond et al. | Feb 1991 | A |
5626022 | Scudder et al. | May 1997 | A |
6103280 | Molzahn | Aug 2000 | A |
6141970 | Molzahn et al. | Nov 2000 | A |
6170283 | Anthony | Jan 2001 | B1 |
7107783 | Smolko et al. | Sep 2006 | B2 |
7117684 | Scudder et al. | Oct 2006 | B2 |
10018395 | Boyd | Jul 2018 | B2 |
20110271692 | Rasmussen | Nov 2011 | A1 |
Entry |
---|
Tom Vanderbilt, Design—Pop Art—The brilliant redesign of the soda can tab, Sep. 24, 2012, The Slate Group LLC, https://slate.com/ (Year: 2012). |
Number | Date | Country | |
---|---|---|---|
Parent | 15932812 | Apr 2018 | US |
Child | 16350484 | US | |
Parent | 14120540 | May 2014 | US |
Child | 15932812 | US |