Thermal gas generator
20210114870 ยท 2021-04-22
Inventors
Cpc classification
C01B2203/0838
CHEMISTRY; METALLURGY
C01B2203/0272
CHEMISTRY; METALLURGY
C06B33/00
CHEMISTRY; METALLURGY
C06B27/00
CHEMISTRY; METALLURGY
B01J19/088
PERFORMING OPERATIONS; TRANSPORTING
C01B2203/0277
CHEMISTRY; METALLURGY
C01B3/22
CHEMISTRY; METALLURGY
International classification
C06B27/00
CHEMISTRY; METALLURGY
C07C4/22
CHEMISTRY; METALLURGY
Abstract
Devices for generating a desired gas or mixture of gases by thermally decomposing a polymer, and methods of making and using such devices, are provided. The resulting gas or mixture of gases, or a fraction thereof, can be used for any suitable purpose, including but not limited to use as an inflating or lifting gas. The devices and methods of the disclosure provide greater mass and volumetric efficiency for gas generation and storage relative to conventional gas generation solutions and are safer and simpler than compressed gas cylinders or liquefied gas storage.
Claims
1. A gas generator device, comprising: a first compartment, containing a heat-generating composition; a second compartment, containing a polymer; and a separator in thermal contact with the first and second compartments, configured to transfer thermal energy generated in the first compartment by reaction of the heat-generating composition to the second compartment to thermally decompose the polymer to release at least one product gas.
2. The gas generator device of claim 1, wherein the heat-generating composition is a thermite composition, comprising a metal and a metal oxide.
3. The gas generator device of claim 2, wherein the metal oxide is selected from the group consisting essentially of vanadium (V) oxide, iron (III) oxide, iron (II,III) oxide, copper (II) oxide, copper (I) oxide, tin (IV) oxide, titanium dioxide, manganese dioxide, manganese (III) oxide, chromium (III) oxide, cobalt (II) oxide, silicon dioxide, nickel (II) oxide, silver oxide, molybdenum trioxide, lead (II,IV) oxide, bismuth (III) oxide, and mixtures thereof, and wherein the metal is selected from the group consisting of aluminum, magnesium, silicon, manganese, alloys of magnesium and aluminum, and mixtures thereof.
4. The gas generator device of claim 2, wherein the thermite composition comprises more than one metal, more than one metal oxide, or both.
5. The gas generator device of claim 1, wherein the polymer is selected from the group consisting of polyethylene, polypropylene, polystyrene, trioxane, polyoxymethylene, and combinations and mixtures thereof.
6. The gas generator device of claim 5, wherein the polymer comprises at least one of high-density polyethylene and low-density polyethylene.
7. The gas generator device of claim 1, wherein the at least one product gas comprises at least one of ethylene gas and hydrogen gas.
8. The gas generator device of claim 1, further comprising an igniter interconnected with the first compartment, configured to induce the reaction in the heat-generating composition upon initiation by one or more of a spark, heat, flame, and friction.
9. The gas generator device of claim 1, further comprising at least one gas transport channel in fluid communication with the second compartment, configured to direct flow of the product gas.
10. The gas generator device of claim 1, wherein the second compartment further contains a catalyst configured to promote the thermal decomposition of the polymer.
11. The gas generator device of claim 1, wherein the thermal decomposition of the polymer releases at least two product gases, and wherein the second compartment further contains a catalyst configured to control the thermal decomposition of the polymer to promote a desired production ratio between two or more of the at least two product gases.
12. The gas generator device of claim 1, further comprising a third compartment in fluid communication with the second compartment, configured to receive the at least one product gas from the second compartment and containing a catalyst configured to promote catalytic reforming of the at least one product gas.
13. The gas generator device of claim 1, configured to promote further decomposition of the at least one product gas to a secondary product gas by at least one of thermal decomposition and catalytic decomposition.
14. The gas generator device of claim 13, wherein the at least one product gas comprises ethylene gas and the secondary product gas comprises hydrogen gas.
15. The gas generator device of claim 1, configured to cool the at least one product gas.
16. The gas generator device of claim 15, further comprising a cooling compartment in fluid communication with the second compartment, configured to receive the at least one product gas from the second compartment and cool the at least one product gas.
17. The gas generator device of claim 1, further comprising a component configured to remove or separate a selected species from the at least one product gas.
18. The gas generator device of claim 17, wherein the component is selected from the group consisting of a condenser, a filter, a sieve, and a trap.
19. A gas generator device configured to release at least one product gas by thermal decomposition of a polymer, comprising: a compartment, containing a heat-generating composition and a polymer; and an igniter interconnected with the compartment, configured to induce a reaction in the heat-generating composition upon initiation by one or more of a spark, heat, flame, and friction, wherein at least one of the following is true: (i) the heat-generating composition and the polymer are physically located in a common chamber; (ii) the heat-generating composition and the polymer are physically mixed together; (iii) the heat-generating composition and the polymer are in direct physical contact; (iv) the heat-generating composition and the polymer are spatially arranged proximate to each other to facilitate transfer of thermal energy generated by the reaction of the heat-generating composition to the polymer; (v) the heat-generating composition is provided as a shaped or molded article comprising voids and the polymer occupies at least a portion of the voids; and (vi) the polymer is provided as a shaped or molded article comprising voids and the heat-generating composition occupies at least a portion of the voids.
20. The gas generator device of claim 19, wherein the heat-generating composition is a thermite composition, comprising a metal and a metal oxide.
21. The gas generator device of claim 20, wherein the metal oxide is selected from the group consisting of vanadium (V) oxide, iron (III) oxide, iron (II,III) oxide, copper (II) oxide, copper (I) oxide, tin (IV) oxide, titanium dioxide, manganese dioxide, manganese (III) oxide, chromium (III) oxide, cobalt (II) oxide, silicon dioxide, nickel (II) oxide, silver oxide, molybdenum trioxide, lead (II,IV) oxide, bismuth (III) oxide, and mixtures thereof, and wherein the metal is selected from the group consisting of aluminum, magnesium, silicon, manganese, an alloy of magnesium and aluminum, and mixtures thereof.
22. The gas generator device of claim 20, wherein the thermite composition comprises more than one metal, more than one metal oxide, or both.
23. The gas generator device of claim 19, wherein the polymer is selected from the group consisting of polyethylene, polypropylene, polystyrene, trioxane, polyoxymethylene, and combinations and mixtures thereof.
24. The gas generator device of claim 23, wherein the polymer comprises at least one of high-density polyethylene and low-density polyethylene.
25. The gas generator device of claim 19, wherein the at least one product gas comprises at least one of ethylene gas and hydrogen gas.
26. The gas generator device of claim 19, further comprising at least one gas transport channel in fluid communication with the compartment, configured to direct flow of the product gas.
27. The gas generator device of claim 19, wherein the at least a portion of the polymer is provided as a pellet or rod having a coating of a heat-resistant material that moderates heat transfer to the polymer.
28. The gas generator device of claim 19, wherein the compartment further contains a catalyst configured to promote the thermal decomposition of the polymer.
29. The gas generator device of claim 28, wherein the catalyst is produced in situ as a byproduct of the reaction of the heat-generating composition.
30. The gas generator device of claim 19, wherein the thermal decomposition of the polymer releases at least two product gases, and wherein the compartment further contains a catalyst configured to promote a desired production ratio between two or more of the at least two product gases.
31. The gas generator device of claim 19, further comprising a second compartment in fluid communication with the first compartment, configured to receive the at least one product gas from the compartment and containing a catalyst configured to promote catalytic reforming of the at least one product gas.
32. The gas generator device of claim 19, configured to promote further decomposition of the at least one product gas to a secondary product gas by at least one of thermal decomposition, catalytic decomposition, and catalytic reformation.
33. The gas generator device of claim 32, wherein the at least one product gas comprises ethylene gas and the secondary product gas comprises hydrogen gas.
34. The gas generator device of claim 19, configured to cool the at least one product gas.
35. The gas generator device of claim 34, further comprising a cooling compartment in fluid communication with the compartment, configured to receive the at least one product gas from the compartment and cool the at least one product gas.
36. The gas generator device of claim 19, further comprising a component configured to remove or separate a selected species from the at least one product gas.
37. The gas generator device of claim 36, wherein the component is selected from the group consisting of a condenser, a filter, a sieve, and a trap.
38. A method for generating at least one product gas, comprising: initiating reaction of a heat-generating composition to release thermal energy; causing the transfer of at least some of the released thermal energy to a polymer; and decomposing, with the thermal energy transferred to the polymer, at least some of the polymer to release the at least one product gas.
39. The method of claim 38, wherein the polymer is a polymer that can decompose to yield ethylene and the at least one product gas comprises ethylene.
40. The method of claim 39, wherein the polymer comprises polyethylene, wherein the heat-generating composition is a thermite composition comprising a metal and a metal oxide, wherein the metal oxide is selected from the group consisting essentially of vanadium (V) oxide, iron (III) oxide, iron (II,III) oxide, copper (II) oxide, copper (I) oxide, tin (IV) oxide, titanium dioxide, manganese dioxide, manganese (III) oxide, chromium (III) oxide, cobalt (II) oxide, silicon dioxide, nickel (II) oxide, silver oxide, molybdenum trioxide, lead (II,IV) oxide, bismuth (III) oxide, and mixtures thereof, and wherein the metal is selected from the group consisting of aluminum, magnesium, silicon, manganese, alloys of magnesium and aluminum, and mixtures thereof.
41. The method of claim 39, wherein the initiating step comprises contacting the heat-generating composition with an igniter initiated by one or more of a spark, heat, flame, and friction.
42. The method of claim 39, wherein thermal energy is transferred from the heat-generating composition to the polymer via a separator.
43. The method of claim 39, wherein the at least one product gas further comprises hydrogen gas.
44. The method of claim 39, further comprising cooling the at least one product gas.
45. The method of claim 38, further comprising inflating an inflatable article with the at least one product gas.
46. The method of claim 45, wherein the inflatable article is selected from the group consisting of a balloon and a float.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0061] The accompanying drawings are incorporated into and form a part of the specification to illustrate several examples of the present disclosure. These drawings, together with the description, explain the principles of the disclosure. The drawings simply illustrate preferred and alternative examples of how the disclosure can be made and used and are not to be construed as limiting the disclosure to only the illustrated and described examples. Further features and advantages will become apparent from the following, more detailed, description of the various aspects, embodiments, and configurations of the disclosure, as illustrated by the drawings referenced below.
[0062]
[0063]
[0064]
[0065]
[0066]
[0067]
[0068]
DETAILED DESCRIPTION
[0069] Devices for generating a desired gas or mixture of gases, and methods for making and using such devices, are provided herein. Compared to conventional devices and systems for gas generation, the devices and systems of the present disclosure may have any one or more of several advantages and benefits, including but not limited to decreased mass, decreased volume or spatial footprint, an ability to generate the desired gas or mixture of gases in greater quantities, and an ability to generate the desired gas or mixture of gases more rapidly.
[0070] In some configurations, a first volume can be filled with a thermite mixture or other heat-generating mixture; such mixture is commonly not gas generating on its own (or is substantially free of gaseous byproduct(s) during release of thermal energy). A second volume can be filled with a gas-generating polymeric composition, such as any one or more of polyethylene, polypropylene, polystyrene, trioxane, and polyoxymethylene, which may be in forms such as but not limited to pellets, sheets, tubes, rods, fibers, or custom molded shapes. The two volumes are commonly in thermal contact with each other, advantageously through a medium that can moderate or control the rate of heat transfer, though such control is not required and is not used in every embodiment.
[0071] To start the generator, the heat-generating material, e.g., thermite mixture (such as but not limited to a mixture of aluminum metal and iron (III) oxide), can be ignited to produce heat. As heat or thermal energy is conducted from the first volume to the second volume, a mixture of gases including, in the case of polyethylene, a substantial portion of ethylene is initially produced as the polyethylene decomposes. This gas mixture may be used as-is, thermally and/or catalytically treated to yield a more desirable gas mixture, and/or have undesirable components removed through means such as but not limited to filters, sieves, traps, or condensers.
[0072] In some configurations, a common volume can be filled with both 1) a thermite mixture or other heat-generating mixture (such mixture is preferably not gas generating on its own), and 2) a gas-generating polymeric composition, such as any one or more of polyethylene, polypropylene, polystyrene, trioxane, and polyoxymethylene, which may be in forms such as but not limited to pellets, sheets, tubes, rods, fibers, or custom molded shapes. The two species can be in thermal contact with each other by virtue of either 1) being a physical mixture, or 2) other direct physical contact, or 3) physical proximity, or 4) being a physical construct in which either the thermite, the polymer, or both are molded shapes, and the one species occupies at least a portion of the voids in the other.
[0073] To start the generator, the thermal-generating material, e.g., thermite mixture (such as but not limited to a mixture of aluminum metal and iron (III) oxide), can be ignited to produce a hot slag. The polyethylene or other polymeric material which is now in direct contact with the slag will thermally decompose yielding a mixture of gases including, in the case of polyethylene, a substantial portion of ethylene. This gas mixture may be used as-is, thermally and/or catalytically treated to yield a more desirable gas mixture, and/or have undesirable components removed through means such as but not limited to filters, sieves, traps, or condensers.
[0074] Various embodiments of the gas generator device will now be discussed with reference to the figures.
[0075]
[0076] The first 101 and second 102 compartments have first and second compartment volumes, respectively. The gas generator device 100 has a device volume. In some configurations the device volume can be the sum of the first 101 and second 102 compartment volumes. In some configurations, the device volume can be more than the sum of the first 101 and second 102 compartment volumes. In some configurations, the first 101 and second 102 compartments can be stacked one atop the other; it will be appreciated that the compartments can be stacked in any order. In other configurations, the first 101 and second 102 compartments can be arranged with one of the compartments partly or completely encased in the other, as for example depicted without limitation in
[0077] In some embodiments, the first compartment 101 is configured with one or more vents (not depicted).
[0078] Most typically, the heat-generating composition comprises a thermite composition, which in turn comprises a metal (i.e. a fuel) and a metal oxide (i.e. an oxidizer). The thermite reaction, i.e. the exothermic reduction-oxidation reaction between a metal fuel and a metal oxide when ignited by heat, has been known for well over a century; see, e.g., U.S. Pat. No. 906,009, entitled Manufacture of thermic mixtures, issued 8 Dec. 1908 to Goldschmidt (Goldschmidt), the entirety of which is incorporated herein by reference. The thermite reaction is generally non-explosive but can create intense heat and high temperatures; it thus finds a variety of useful applications, (e.g. welding, metal refining, disabling munitions, incendiary weapons, and pyrotechnic initiators) and so is widely, and (for many formulations) inexpensively, available from many suppliers. The metal may, but need not, be selected from the group consisting essentially of vanadium (V) oxide, iron (III) oxide, iron (II,III) oxide, copper (II) oxide, copper (I) oxide, tin (IV) oxide, titanium dioxide, manganese dioxide, manganese (III) oxide, chromium (III) oxide, cobalt (II) oxide, silicon dioxide, nickel (II) oxide, silver oxide, molybdenum trioxide, lead (II,IV) oxide, bismuth (III) oxide, and combinations thereof, and the metal may, but need not, be selected from the group consisting of aluminum, magnesium, silicon, manganese, an alloy of magnesium and aluminum, and combinations thereof. The thermite composition may, but need not, comprise more than one metal, more than one metal oxide, or both.
[0079] In one configuration, the heat-generating composition comprises a thermite composition that comprises a mixture of ferric oxide and aluminum. The chemical reaction of this thermite mixture is shown below in chemical equation (1):
Fe.sub.2O.sub.3(s)+2Al(s).fwdarw.2Fe(s)+Al.sub.2O.sub.3(s)(1)
[0080] The thermite chemical reaction is exothermic and releases a large quantity of thermal energy, resulting in temperatures sufficient to produce an aluminum oxide slag and molten iron. The enthalpy or heat of reaction (H value) for the thermite reaction is about 849 k (e.g., 849 kJ per mole Fe.sub.2O.sub.3). The thermite reaction does not require external oxygen and can, therefore, proceed in locations with limited or no air flow (e.g. in space), or even under water. Furthermore, the reaction of many types and mixtures of thermite does not produce any gases which might carry away some of the heat of the reaction or produce an explosive excess of pressure.
[0081] It can be appreciated that the heat-generating composition can generate very large amounts of thermal energy per unit mass of the heat-generating composition. A compact gas generating system can thus be achieved by producing such large amounts of thermal energy per unit mass of the heat-generating composition. Furthermore, in many embodiments, substantially most of the heat generated remains available to decompose the polymer because gaseous byproducts are not produced; that is, most of the heat is retained in the liquid and/or solid reaction products as a source of thermal energy.
[0082] Typically, at least some of the thermal energy transferred to the second compartment 102 by the separator 103 thermally decomposes some of the polymer contained in the second compartment 102. The thermal decomposition of the polymer releases one or more product gases. By way of non-limiting example, polyethylene can be thermally decomposed to ethylene gas, and in some embodiments at least a portion of the ethylene gas may be secondarily decomposed (either thermally or catalytically) to hydrogen gas.
[0083] In some embodiments, at least about 99 mole % of the polymer may be converted to the one or more product gases. More generally, at least 95 mole %, even more generally at least about 90 mole %, yet even more generally at least about 80 mole %, still yet even more generally at least about 70 mole %, still yet even more generally at least about 60 mole %, still yet even more generally at least about 50 mole %, still yet even more generally at least about 40 mole %, still yet even more generally at least about 30 mole %, still yet even more generally at least about 20 mole %, or yet still even more generally at least about 10 mole % of the polymer may be converted to the one or more product gases.
[0084] It can be appreciated that, in many embodiments, there is no need to control one or both of the temperature or thermal energy transfer within the device 100. As a result, the device 100 can be configured to transfer thermal energy rapidly between the first 101 and second 102 compartments, thereby decomposing the polymer to release the one or more product gases more rapidly than current gas generation systems. Moreover, the device 100 can be more easily constructed and operated than other gas generators; for example, there is not always a need to have the polymer decomposition occur at any specific temperature, so neither the reaction of the heat-generating composition nor the transfer of thermal energy from the first 101 to the second 102 compartment must necessarily be regulated. This contrasts with catalytic decomposition methods, which require the catalyst to be operated at specific temperatures, pressures, and reactant flow rates. Even more advantageously, in those embodiments where control over one or both of the temperature or the rate of energy transfer within the device 100 is required or desired, such control can be achieved by varying the chemical makeup of the thermite or other heat-generating composition within the first compartment 101, without the need to rebuild or retrofit the device 100 itself.
[0085] The gas generator device 100 may further include an igniter 104 interconnected with the first compartment. The igniter 104 causes the ignition of the heat-generating composition. In some configurations, a spark generated within the igniter 104 initiates the ignition process. In other configurations, the ignition process is initiated by thermal energy generated within the igniter 104. The thermal energy provided within igniter 104 may be from a hot wire. In other configurations, the initiating energy within igniter 104 may be from flame. In other configurations, the initiating energy within the igniter 104 may be provided by friction.
[0086] The igniter 104 may further comprise an ignition aperture in the first compartment 101. The ignition aperture may be configured with a safety-delay switch system.
[0087] The gas generator device 100 may further include a heat exchanger 106 interconnected with the second compartment 102. The heat exchanger 106 is configured to cool the product gas(es) released from the polymer. In accordance with some embodiments, the heat exchanger 106 may be interconnected to outlet 107a of the second compartment 102. The exchanger 106 cools the product gas(es) exiting the second compartment 102 through outlet 107a and releases the cooled gas through outlet 107b.
[0088] It is to be expressly understood that that the first 101 and second 102 compartments can be spatially arranged in any suitable configuration. By way of non-limiting example, in some embodiments, the compartments can be stacked atop each other, while in other embodiments one of the compartments can be partially or completely encased within or surrounded by the other compartment.
[0089]
[0090] In step 210, reaction of a heat-generating composition is initiated in a first compartment 101. The reaction releases thermal energy. The heat-generating composition may be a thermite composition comprised of a metal and a metal oxide. The metal may, but need not, be selected from the group consisting of vanadium (V) oxide, iron (III) oxide, iron (II,III) oxide, copper (II) oxide, copper (I) oxide, tin (IV) oxide, titanium dioxide, manganese dioxide, manganese (III) oxide, chromium (III) oxide, cobalt (II) oxide, silicon dioxide, nickel (II) oxide, silver oxide, molybdenum trioxide, lead (II,IV) oxide, bismuth (III) oxide, and combinations thereof, and the metal may, but need not, be selected from the group consisting of aluminum, magnesium, silicon, manganese, an alloy of magnesium and aluminum, and combinations thereof. The thermite composition may, but need not, comprise more than one metal, more than one metal oxide, or both.
[0091] Step 210 may further include contacting the heat-generating composition with an igniter to initiate the reaction. In some configurations the reaction may be initiated by contacting the igniter with one of a hot wire or a spark. In other configurations, flame may initiate the reaction of the heat-generating composition via the igniter. In yet other configurations, friction may initiate reaction of the heat-generating composition via the igniter.
[0092] In step 220, the energy released by the reaction of the heat-generating composition is transferred from the first compartment 101 to a second compartment 102. A polymer is contained in the second compartment. Non-limiting examples of the polymer include various forms of polyethylene (e.g. low-density polyethylene (LDPE), high-density polyethylene (HDPE), and mixtures thereof), polypropylene, polystyrene, trioxane, and polyoxymethylene.
[0093] In step 230, the thermal energy transferred to the second compartment 102 decomposes the polymer to release one or more product gases. Step 230 may further include transferring the released thermal energy from the first compartment 101 to the second compartment 102 through a separator 103. The material and construction of the separator 103, and the composition and amount of the polymer in the second compartment 102, can be selected to provide for a desired amount or rate of production of the product gas(es).
[0094] In optional step 240, the released product gas(es) may be cooled, in some embodiments by a heat exchanger.
[0095] In optional step 250, the released gas may be used for one of: inflation of a meteorological balloon; inflation of other types of balloons; inflation of a blimp; inflation of a HIAD; inflation of an inflatable article; pressurization of a gas storage cylinder; and the like.
[0096]
[0097]
[0098] In accordance with some embodiments, the compartment 101 may be defined by a wall 111.
[0099] Typically, at least some of the thermal energy available to the polymer due to the reaction of the heat-generating composition in the compartment 101 thermally decomposes some of the polymer contained in the compartment 101. The thermal decomposition of the polymer releases one or more product gases. By way of non-limiting example, polyethylene can be thermally decomposed to ethylene gas, and in some embodiments at least a portion of the ethylene gas may be secondarily decomposed (either thermally or catalytically) to hydrogen gas.
[0100] In some embodiments, at least about 99 mole % of the polymer may be converted to the one or more product gases. More generally, at least 95 mole %, even more generally at least about 90 mole %, yet even more generally at least about 80 mole %, still yet even more generally at least about 70 mole %, still yet even more generally at least about 60 mole %, still yet even more generally at least about 50 mole %, still yet even more generally at least about 40 mole %, still yet even more generally at least about 30 mole %, still yet even more generally at least about 20 mole %, or yet still even more generally at least about 10 mole % of the polymer may be converted to the one or more product gases.
[0101] It can be appreciated that, in many embodiments, there is no need to control one or both of the temperature or thermal energy transfer within the device 100. Moreover, the device 100 can be more easily constructed and operated than other gas generators; for example, the absence of a second compartment may simplify the design of the device 100 and be suitable for applications in which transfer of substantially all of the thermal energy generated by reaction of the heat-generating composition to the polymer is desirable. Even more advantageously, in those embodiments where control over one or both of the temperature or the rate of energy transfer within the device 100 is required or desired, such control can be achieved by varying the chemical makeup of the thermite or other heat-generating composition within the compartment 101, and/or the spatial arrangement of the polymer relative to the heat-generating composition in the compartment 101, without the need to redesign the device 100 itself.
[0102] The gas generator device 100 may further include an igniter 104 interconnected with the compartment 101. The igniter 104 causes the ignition of the heat-generating composition. In some configurations, a spark generated within the igniter 104 initiates the ignition process. In other configurations, the ignition process is initiated by thermal energy generated within the igniter 104. The thermal energy provided within igniter 104 may be from a hot wire. In other configurations, the initiating energy within igniter 104 may be from flame. In other configurations, the initiating energy within the igniter 104 may be provided by friction.
[0103] The igniter 104 may further comprise an ignition aperture in the compartment 101. The ignition aperture may be configured with a safety-delay switch system.
[0104] The gas generator device 100 may further include a heat exchanger 106 interconnected with the compartment 101. The heat exchanger 106 is configured to cool the product gas(es) released from the polymer. In accordance with some embodiments, the heat exchanger 106 may be interconnected to outlet 107a of the compartment 101. The exchanger 106 cools the product gas(es) exiting the compartment 101 through outlet 107a, with the cooled gas exiting the exchanger 106 via outlet 107b.
[0105]
[0106] Typically, at least some of the thermal energy available to the polymer due to the reaction of the heat-generating composition in the compartment 101 thermally decomposes some of the polymer contained in the compartment 101. The thermal decomposition of the polymer releases one or more product gases. By way of non-limiting example, polyethylene can be thermally decomposed to ethylene gas, and in some embodiments at least a portion of the ethylene gas may be secondarily decomposed (either thermally or catalytically) to hydrogen gas.
[0107] In some embodiments, at least about 99 mole % of the polymer may be converted to the one or more product gases. More generally, at least 95 mole %, even more generally at least about 90 mole %, yet even more generally at least about 80 mole %, still yet even more generally at least about 70 mole %, still yet even more generally at least about 60 mole %, still yet even more generally at least about 50 mole %, still yet even more generally at least about 40 mole %, still yet even more generally at least about 30 mole %, still yet even more generally at least about 20 mole %, or yet still even more generally at least about 10 mole % of the polymer may be converted to the one or more product gases.
[0108] It can be appreciated that, in many embodiments, there is no need to control one or both of the temperature or thermal energy transfer within the device 100. Moreover, the device 100 can be more easily constructed and operated than other gas generators; for example, the absence of a second compartment may simplify the design of the device 100 and be suitable for applications in which transfer of substantially all of the thermal energy generated by reaction of the heat-generating composition to the polymer is desirable. Even more advantageously, in those embodiments where control over one or both of the temperature or the rate of energy transfer within the device 100 is required or desired, such control can be achieved by varying the chemical makeup of the thermite or other heat-generating composition within the compartment 101, and/or the spatial arrangement of the polymer relative to the heat-generating composition in the compartment 101, without the need to redesign the device 100 itself.
[0109] The gas generator device 100 may further include an igniter 104 interconnected with the compartment 101. The igniter 104 causes the ignition of the heat-generating composition. In some configurations, a spark generated within the igniter 104 initiates the ignition process. In other configurations, the ignition process is initiated by thermal energy generated within the igniter 104. The thermal energy provided within igniter 104 may be from a hot wire. In other configurations, the initiating energy within igniter 104 may be from flame. In other configurations, the initiating energy within the igniter 104 may be provided by friction.
[0110] The igniter 104 may further comprise an ignition aperture in the compartment 101. The ignition aperture may be configured with a safety-delay switch system.
[0111] The gas generator device 100 may further include a heat exchanger 106 interconnected with the compartment 101. The heat exchanger 106 is configured to cool the product gas(es) released from the polymer. In accordance with some embodiments, the heat exchanger 106 may be interconnected to outlet 107a of the compartment 101. The exchanger 106 cools the product gas(es) exiting the compartment 101 through outlet 107a, with the cooled gas exiting the exchanger 106 via outlet 107b.
[0112]
[0113] In step 610, reaction of a heat-generating composition is initiated in a compartment 101. The reaction releases thermal energy. The heat-generating composition may comprise a thermite composition comprising a metal and a metal oxide. The metal may, but need not, be selected from the group consisting of vanadium (V) oxide, iron (III) oxide, iron (II,III) oxide, copper (II) oxide, copper (I) oxide, tin (IV) oxide, titanium dioxide, manganese dioxide, manganese (III) oxide, chromium (III) oxide, cobalt (II) oxide, silicon dioxide, nickel (II) oxide, silver oxide, molybdenum trioxide, lead (II,IV) oxide, bismuth (III) oxide, and combinations thereof, and the metal may, but need not, be selected from the group consisting of aluminum, magnesium, silicon, manganese, an alloy of magnesium and aluminum, and combinations thereof. The thermite composition may, but need not, comprise more than one metal, more than one metal oxide, or both.
[0114] Step 610 may further include contacting the heat-generating composition with an igniter to initiate the reaction. In some configurations the reaction may be initiated by contacting the igniter with one of a hot wire or a spark. In other configurations, flame may initiate the reaction of the heat-generating composition via the igniter. In yet other configurations, friction may initiate reaction of the heat-generating composition via the igniter.
[0115] In step 620, the thermal energy generated by reaction of the heat-generating composition decomposes a polymer in the compartment 101 to release one or more product gases. In contrast to the device depicted in
[0116] In optional step 630, the released product gas(es) may be cooled, in some embodiments by a heat exchanger.
[0117] In optional step 640, the released gas may be used for one of: inflation of a meteorological balloon; inflation of other types of balloons; inflation of a blimp; inflation of a HIAD; inflation of an inflatable article; pressurization of a gas storage cylinder; and the like.
[0118]
[0119] In step 710, reaction of a heat-generating composition is initiated in a compartment. The reaction releases thermal energy. The heat-generating composition may comprise a thermite composition comprising a metal and a metal oxide. The metal may, but need not, be selected from the group consisting of vanadium (V) oxide, iron (III) oxide, iron (II,III) oxide, copper (II) oxide, copper (I) oxide, tin (IV) oxide, titanium dioxide, manganese dioxide, manganese (III) oxide, chromium (III) oxide, cobalt (II) oxide, silicon dioxide, nickel (II) oxide, silver oxide, molybdenum trioxide, lead (II,IV) oxide, bismuth (III) oxide, and combinations thereof, and the metal may, but need not, be selected from the group consisting of aluminum, magnesium, silicon, manganese, an alloy of magnesium and aluminum, and combinations thereof. The thermite composition may, but need not, comprise more than one metal, more than one metal oxide, or both.
[0120] Step 710 may further include contacting the heat-generating composition with an igniter to initiate the reaction. In some configurations the reaction may be initiated by contacting the igniter with one of a hot wire or a spark. In other configurations, flame may initiate the reaction of the heat-generating composition via the igniter. In yet other configurations, friction may initiate reaction of the heat-generating composition via the igniter.
[0121] In step 720, the thermal energy generated by reaction of the heat-generating composition decomposes a polymer in the compartment to release one or more product gases. Step 720 may in some embodiments include or require transfer of thermal energy to a separate compartment via a separator, as in the device depicted in
[0122] In step 730, the one or more product gases are subjected to further chemical processing. Particularly, step 730 may in embodiments include reformation of one or more product gases. In such embodiments, the method 700 may employ a catalyst configured to facilitate catalytic reformation of the one or more product gases. Such catalyst may be provided in any desired spatial arrangement (e.g. a fixed bed), and may be present either in the compartment in which the one or more product gases are formed (i.e. the compartment containing the polymer), or in a separate compartment configured to receive the one or more product gases.
[0123] In optional step 740, the released product gas(es) may be cooled, in some embodiments by a heat exchanger.
[0124] In optional step 750, the released gas may be used for one of: inflation of a meteorological balloon; inflation of other types of balloons; inflation of a blimp; inflation of a HIAD; inflation of an inflatable article; pressurization of a gas storage cylinder; and the like.
[0125] Embodiments of the devices and methods disclosed herein may be directed to the thermal decomposition of any one or more polymers such as polyethylene, polypropylene, polystyrene, trioxane, polyoxymethylene, and combinations and mixtures thereof.
[0126] Embodiments of the devices and methods disclosed herein may be directed to the production of any one or more product gases, but particularly may be directed to the production of ethylene gas, and/or (either directly or by secondary thermal or catalytic decomposition of ethylene) hydrogen gas. Ethylene gas, or hydrogen gas, or the combination of ethylene and hydrogen gases may, in embodiments, generally make up at least about 75 mol %, more generally at least about 70 mol %, even more generally at least about 65 mol %, yet even more generally at least about 60 mol %, still yet even more generally at least about 55 mol %, still yet even more generally at least about 50 mol %, still yet even more generally at least about 45 mol %, still yet even more generally at least about 40 mol %, still yet even more generally at least about 35 mol %, still yet even more generally at least about 30 mol %, or still yet even more generally at least about 25 mol % of the total product gas content.
[0127] In embodiments of the devices and methods disclosed herein, the composition of the product gas(es) may be such that it is not necessary to provide additional heat or other (or, in some cases, any) energy inputs to maintain most or all of the product gas(es) in the desired gaseous state after formation of the gas. By way of non-limiting example, the product gas(es) may in some embodiments be passively or actively cooled to ambient or near-ambient temperatures (e.g. at least substantially, if not entirely, free of added heat or thermal energy relative to ambient conditions), without risk of undesirable condensation of product gas(es). In this way, the devices and methods disclosed herein may advantageously serve differing purposes relative to gas generation devices and methods of the prior art.
[0128] In some embodiments, the precise chemical composition or properties of the one or more product gas(es) are not a consideration, or at least are not as crucial a consideration as the rate or amounts (whether molar or mass amounts) in which the product gas(es) can be generated; by way of non-limiting example, it may be desirable to produce as great a molar quantity of gas as possible to inflate an inflatable article to the greatest extent possible, since volume is directly related not to mass of the gas but to its molar quantity. In these applications, it may be desirable to cause the polymer to decompose in the first instance, and/or to cause one or more product gas(es) to undergo secondary decomposition, into as small (in molecular weight terms) a gas as possible to increase the volume of gas produced without requiring additional mass of materials. One such desirable small gas is hydrogen gas (H.sub.2). Thus, in embodiments, a heat-generating composition may be provided that provides temperatures great enough to rapidly facilitate decomposition of, e.g., ethylene gas (produced, e.g., by decomposition of polyethylene) to hydrogen gas. In other embodiments, a catalyst may be provided in the compartment containing the polymer that catalyzes the decomposition of a product gas into hydrogen gas or another small gas.
[0129] In some embodiments, it may be necessary to minimize or eliminate byproducts, impurities, and other undesirable species in the product gas(es). However, limitations on the availability of a suitable polymer may necessitate the use of a polymer that is susceptible to the production of such byproducts, impurities, and undesirable species. By way of non-limiting example, higher hydrocarbons such as C4 hydrocarbons may be produced when decomposing polymers such as polyethylene, polypropylene, polystyrene, trioxane, or polyoxymethylene, which could be undesirable due to condensation in low-temperature applications. Thus, devices and systems of the present disclosure may include one or more filters, sieves, traps, condensers, or other similar components to selectively remove an identified undesirable species from the product gas(es). Such components can be provided in association with the compartment in which the product gas(es) is/are formed by decomposition of the polymer, or they can be provided in association with a separate compartment into which the one or more product gases flow after formation.
[0130] In some embodiments, it may be desirable to provide for further chemical processing of the one or more product gases. Particularly, it may be desirable to provide for subsequent chemical reaction of one or more product gases, e.g. gas production or gas reformation. In such embodiments, the devices and methods of the invention may employ a catalyst configured to facilitate such chemical processing of the one or more product gases. Such catalyst may be provided in any desired spatial arrangement (e.g. a fixed bed), and may be present either in the compartment in which the one or more product gases are formed (i.e. the compartment containing the polymer), or in a separate compartment configured to receive the one or more product gases.
[0131] In embodiments of the present disclosure, the polymer may be selected based on the identity of the gas or gases desired to be produced. By way of non-limiting example, where a gas desired to be produced is ethylene gas, polyethylene may be selected as the polymer. In some embodiments, the desired gas may be a secondary decomposition product, i.e. a gas that is produced by first thermally decomposing the polymer into an intermediate species and then further thermally or catalytically decomposing the intermediate species to the desired gas, and the polymer may be selected accordingly; by way of non-limiting example, where a desired gas is hydrogen gas, polyethylene may be selected as the polymer, and the gas generator device 100 may be configured to first decompose the polyethylene to ethylene gas and subsequently (due to, e.g., increased temperature or the presence of a catalyst) decompose the ethylene gas to hydrogen gas. Other polymers suitable for producing these or other product gases include polypropylene, polystyrene, trioxane, and polyoxymethylene.
[0132] In embodiments of the present disclosure, the polymer may be provided in any suitable physical form. By way of first non-limiting example, the polymer may be provided in a physical form comprising one or more pellets. By way of second non-limiting example, the polymer may be provided in a physical form comprising one or more sheets. By way of third non-limiting example, the polymer may be provided in a physical form comprising one or more tubes. By way of fourth non-limiting example, the polymer may be provided in a physical form comprising one or more rods. By way of fifth non-limiting example, the polymer may be provided in a physical form comprising one or more fibers. By way of sixth non-limiting example, the polymer may be provided in a physical form comprising one or more molded shapes or articles.
[0133] While the foregoing disclosure has generally focused on the production of gases in the context of inflating an inflatable article, it is to be expressly understood that the devices and methods of the disclosure are suitable to produce one or more product gases for any desired application. By way of first non-limiting example, the devices and methods of the disclosure may be used to fill or pressurize a cylinder, tank, or vessel, e.g. a storage cylinder or tank, with a desired gas. By way of second non-limiting example, the devices and methods of the disclosure may be used to produce a lifting gas to be used in, e.g., a buoyant vehicle or article such as a hot air balloon or a float. By way of third non-limiting example, the devices and methods of the disclosure may be used to produce a selected atmosphere within a volume, e.g. ethylene gas may be produced and used in a ripening room to accelerate the ripening of fruits and vegetables. These and other applications are within the scope of the present disclosure.
[0134] Several variations and modifications of the disclosure can be used. It would be possible to provide for some features of the disclosure without providing others.
[0135] The present disclosure, in various aspects, embodiments, and configurations, includes components, methods, processes, systems and/or apparatus substantially as depicted and described herein, including various aspects, embodiments, configurations, sub-combinations, and subsets thereof. Those of skill in the art will understand how to make and use the various aspects, embodiments, and configurations, after understanding the present disclosure. The present disclosure, in various aspects, embodiments, and configurations, includes providing devices and processes in the absence of items not depicted and/or described herein or in various aspects, embodiments, and configurations hereof, including in the absence of such items as may have been used in previous devices or processes, e.g., for improving performance, achieving ease and/or reducing cost of implementation.
[0136] The foregoing discussion of the disclosure has been presented for purposes of illustration and description. The foregoing is not intended to limit the disclosure to the form or forms disclosed herein. In the foregoing Detailed Description for example, various features of the disclosure are grouped together in one or more, aspects, embodiments, and configurations for the purpose of streamlining the disclosure. The features of the aspects, embodiments, and configurations of the disclosure may be combined in alternate aspects, embodiments, and configurations other than those discussed above. This method of disclosure is not to be interpreted as reflecting an intention that the claimed disclosure requires more features than are expressly recited in each claim. Rather, as the following claims reflect, inventive aspects lie in less than all features of a single foregoing disclosed aspect, embodiment, or configuration. Thus, the following claims are hereby incorporated into this Detailed Description, with each claim standing on its own as a separate preferred embodiment of the disclosure.
[0137] Moreover, though the description of the disclosure has included description of one or more aspects, embodiments, or configurations and certain variations and modifications, other variations, combinations, and modifications are within the scope of the disclosure, e.g., as may be within the skill and knowledge of those in the art, after understanding the present disclosure. It is intended to obtain rights which include alternative aspects, embodiments, and configurations to the extent permitted, including alternate, interchangeable and/or equivalent structures, functions, ranges or steps to those claimed, whether or not such alternate, interchangeable and/or equivalent structures, functions, ranges or steps are disclosed herein, and without intending to publicly dedicate any patentable subject matter.