SHIPPING CONTAINER THAT HAS A FLAME RETARDANT LAYER AND A THERMAL BLOCKING LAYER

专利摘要:
The present invention relates to a transport container (10) for transporting thermally active materials (14) that includes a plurality of structuring panels (16) that define an inner container (18), and are configured to receive the materials. thermally active (14). the container (10) also includes an exterior disposed adjacent an environment (e) in which the transport container (100) is disposed. a thermal barrier member (24) may be disposed between the thermally active materials and the environment (e) in which the container is disposed. the thermal barrier (10) includes an interior thermal barrier panel (28) and an exterior thermal barrier panel (32) that define a heat-absorbing material receiving cavity (34). a flowable polymer based on heat absorbing material is disposed within the heat absorbing material receiving cavity (34). the thermal barrier (24) is configured to substantially surround the thermally active materials (14) to reduce the passage of thermal energy between the thermally active materials (14) and the environment (e) in which the transport container (100) is disposed .
公开号:BR112017003400B1
申请号:R112017003400-0
申请日:2015-08-26
公开日:2022-01-11
发明作者:Dennis Campbell；Carl Gehlhausen
申请人:Nochar, Inc；
IPC主号:

专利说明:

I. Technical Field of Invention
[001] The present invention relates to containers and packaging materials, and more particularly to a container having a thermal barrier member to reduce heat transfer from and/or to the container. II. Background of the invention
[002] With the proliferation of "devices", electrically operated portables, the number of batteries sold to power these devices grew proportionately. One type of battery whose sales have increased dramatically over the last 10 years is the lithium battery. For example, it is estimated that about $4 million worth of lithium batteries were sold in 1996, and that about $4 billion worth of lithium batteries were sold in 2014.
[003] Lithium batteries have advantages over alkaline batteries which they generally replace. Because lithium is a very active material, it tends to provide more energy in relation to the amount of material used in the battery. Additionally, the lithium discharge curve is longer and flatter than alkaline, thus providing consistently higher voltage for battery life.
[004] Said features allow a device manufacturer to reduce the size of batteries of equivalent power required to operate the device, or alternatively to provide a greater amount of battery power in a given size.
[005] Although lithium batteries are more expensive than alkaline, they have especially good performance characteristics when used in small devices or those that need a large amount of backup power, such as cameras and smartphones.
[006] The term "lithium battery" refers to a class of batteries that includes cathodes or electrolytes that contain either metallic lithium or a lithium compound. The two main categories of lithium batteries include lithium metal batteries and lithium-ion batteries.
[007] There are several important differences between lithium batteries and lithium-ion batteries. The most important practical difference between the two is that lithium batteries are not rechargeable, whereas lithium-ion batteries are rechargeable. From a chemical point of view, lithium batteries use lithium in its pure metallic form, while lithium-ion batteries use lithium compounds that are much more stable than the elemental lithium used in lithium batteries. While lithium batteries can never be recharged, lithium-ion batteries are designed to be recharged hundreds of times.
[008] Another advantage of lithium batteries over other rechargeable batteries such as rechargeable nickel metal hydride batteries or nickel cadmium batteries is that lithium batteries have a higher energy density than most types of batteries. other rechargeables. As such, for the size and weight, lithium-ion batteries can store more energy than nickel-based rechargeable batteries.
[009] Additionally, lithium-ion batteries operate at higher voltages than other rechargeable batteries, which allow single cell batteries to be used in many applications while nickel-metal hydride batteries or nickel-plated batteries do. Cadmium require multiple cells. Additional lithium batteries have a lower self-discharge coefficient than other types of rechargeable batteries, and therefore retain their charge for a longer period of time. In short, lithium-ion batteries can be made to be smaller, lighter, have a high voltage, and hold a much longer charge than other types of rechargeable batteries.
[0010] Unfortunately, lithium batteries also have certain disadvantages when compared to other batteries. For example, lithium batteries can be more uneconomical to manufacture than alkaline batteries and nickel-based batteries. Another disadvantage of using lithium batteries is that they have a greater potential to catch fire than nickel-based batteries.
[0011] The root cause of Li-ion batteries' propensity to catch fire is believed to be a failure or a defect in the separators inside the batteries. Lithium batteries contain extremely thin separators that keep the elements in the battery separate. When said separators fail to function properly, the battery can fail and catch fire. Said "bad separator" faults can result from poor design, manufacturing defects, externally induced battery damage, poor battery packaging design, insufficient or inadequate protection being configured into the battery design, and overcharging.
[0012] The internal short circuit resulting from damage to the thin separator results in subsequent heat build-up. Said heat build-up in a particular battery can trigger what is known as a thermal runaway in which the battery will overheat and burst into flames, and thereby ignite adjacent batteries in much the same way as a lit match inside a box of matches. will ignite adjacent matches if the lit match approaches adjacent unlit matches.
[0013] In this regard, it has been recognized that Li-ion batteries ignite at about (953 degrees F), and can reach temperatures that exceeds (1100 degrees F) during burning. As such, a burning lithium-ion battery can often generate enough heat to cause adjacent batteries to ignite as well.
[0014] Said ability of batteries to ignite other batteries is referred to as a "thermal runaway". One factor that exacerbates thermal runaway is that lithium batteries are capable of igniting and catching fire without the presence of oxygen. As such, placing the batteries in a vacuum container, or a sealed container, will not prevent the batteries within the container from engaging in a thermal runaway and thereby overheating the container.
[0015] Examples have been reported where a container of multiple batteries engaged in thermal runaway caused containers containing multiple adjacent batteries to become hot enough to ignite the lithium batteries contained therein.
[0016] Said propensity to catch fire can increase the risk to carriers carrying lithium batteries, especially when the batteries are carried on board an aircraft. The greater risks of transporting batteries increase the cost of transporting the batteries.
[0017] Transport costs can contribute significantly to battery costs, especially in view of the fact that most batteries that are sold today are manufactured in China, but can be used in distant markets such as China's markets. North America and Europe.
[0018] Thermal runaway can create an especially problematic situation on an aircraft that is carrying a charge of batteries. Tests conducted by the FAA Wiliman J. Hughes Technical Center ("FAA Tech Center") indicate that there are particular propagation characteristics that are associated with lithium batteries. The chain reaction thermal runaway can lead to self-heating and release of energy stored in the battery. In a fire situation, the air temperature in a fire in a cargo hold can rise above the self-ignition temperature of lithium. As discussed above said high temperatures can ignite and propagate ignition of adjacent batteries, and thereby create a risk of a catastrophic fire event in the cargo compartment.
[0019] Although improvements in the construction of lithium-ion batteries have been made to said extremely rare thermal runaway, the risk of a thermal runaway still exists.
[0020] Several attempts have been implemented to control the thermal runaway. Most of these attempts have centered around the use of flame retardant technologies or liquid suppression products.
[0021] The underlying theory behind these attempts is to extinguish fire, and thereby reduce the effective number of batteries that ignite before the fire spreads to adjacent batteries and/or adjacent containers and batteries, rather than preventing the first or for thermal runaway to occur. Unfortunately, said prior art attempts have not been successful to prevent thermal runaway with lithium batteries.
[0022] It will be appreciated that it would be useful to have a container that can limit the impact of said fires and explosions by providing a thermal barrier that reduces heat transfer between adjacent containers, and thereby reduces the amount and size of thermal runaway, and thereby reducing the heat and pressure generated in an area by thermal runaway.
[0023] Superabsorbent polymers (SAPs) or hydrogels are loosely crosslinked, three-dimensional networks of flexible polymer chains that carry dissociated ionic functional groups. The same are basically materials that can absorb fluids of more than 15 times their own dry weight, either under load or without load, such as water, electrolyte solution, synthetic urine, brines, biological fluids such as urine, sweat and blood. The same are polymers which are characterized by carboxylic acid containing hydrophilicity, carboxamide, hydroxyl, amine, imide groups and so on, insoluble in water, and are cross-linked polyelectrolytes. By virtue of their ionic nature and interconnected structure, they absorb large amounts of water and other aqueous solutions without dissolving by solvating water molecules through hydrogen bonds, which increases the entropy of the network making the SAPs swell tremendously. .
[0024] The factors that provide absorption energy to polymers are osmotic pressure, based on mobile counterions, and affinity between the polymer's electrolyte and water. The factor that suppresses absorption energy, differently, is found in the elasticity of the gel that results from its lattice structure. Not only are they of high fluid absorption capacity, but the absorbed fluid is difficult to release, as they merely immobilize the fluid by trapping rather than keeping it in the structure. The process for preparing the same is described, for example, in S. Kiatkamjornwong, "Superabsorbent Polymers and Superabsorbent Polymer Compositions, ScienceAsia, 33 Supplement 1 (2007): 39-43 and MJ Zohuriaan-Mehr and K. Kabiri, "Superabsorbent Polymer Materials: A Review", Iranian Polymer Journal, 17(6), (2008), 451-477.
[0025] There are a number of US patents that address the use of particulate superabsorbent dry polymers for use in flame prevention and flame extinguishing, which include: von Blucher US Patent No. 4,978,460; von Blucher US Patent No. 5,190,110; and US Patent No. 5,849,210. III. Summary of the Invention
[0026] A transport container is configured for transporting thermally active materials. The shipping container comprises a plurality of structuring panels that define an inner container configured to receive the thermally active materials. The container also includes an exterior disposed adjacent an environment in which the shipping container is disposed. The thermal barrier member may be disposed between the thermally active materials and the environment in which the container is disposed. The thermal barrier includes an interior thermal barrier panel and a third exterior barrier panel that defines a heat-absorbing material receiving cavity. A flowable polymer based on heat absorbing material is disposed within the heat absorbing material receiving cavity. The thermal barrier is configured to substantially surround the thermally active materials to reduce the passage of thermal energy between the thermally active materials and the environment in which the shipping container is disposed.
[0027] In a preferred embodiment, the transport container may include a pressure release member to allow pressure generated by the thermally active materials to be vented to the outside of the container.
[0028] In another preferred embodiment, a transport container includes a split member disposed within the heat-absorbing material receiving cavity. The split member defines a series of cells that are configured to receive and retain the flow-capable polymer based heat-absorbing material, so that the heat-absorbing material is dispersed through the material-receiving cavity. heat absorption.
[0029] In a more preferred embodiment, the thermally active materials comprise lithium batteries, and the thermal barrier is capable of maintaining an environment in which the shipping container is disposed at less than about 950 degrees during a sustained burn. of the batteries arranged inside the container inside the thermal barrier.
[0030] In one embodiment, the polymer-based heat absorbing material comprises a superabsorbent polymer.
[0031] In another embodiment, the polymer-based heat-absorbing material essentially consists of a superabsorbent polymer.
[0032] In another embodiment, the polymer-based heat absorbing material consists of a superabsorbent polymer.
[0033] In another embodiment, the superabsorbent polymer is hydrated with water.
[0034] In another embodiment, the superabsorbent polymer is dried.
[0035] In another embodiment, the superabsorbent polymer is a homopolymer.
[0036] In another embodiment, the superabsorbent polymer is a copolymer.
[0037] In another embodiment, the superabsorbent polymer is cationic (a basic water-absorbing resin).
[0038] In another embodiment, the superabsorbent polymer is anionic (an acidic water-absorbing resin).
[0039] In another embodiment, the superabsorbent polymer is a polymer of hydrophilic monomers that contain a carboxylic acid or acid, acid anhydride group, or sulfonic acid group.
[0040] In another embodiment, the superabsorbent polymer is a polymer of hydrophilic monomers that contains a carboxylic acid or sulfonic acid ester, hydroxyl, amide, amine, nitrile, or quaternary ammonium salt group.
[0041] In another embodiment, the superabsorbent polymer is a polymer of hydrophilic monomers selected from the group consisting of: acrylamide, an acrylic acid derivative, maleic acid anhydride, itaconic acid, 2-hydroxy ethyl acrylate, polyethylene glycol, allyl methacrylate, tetraethylene glycol dimethacrylate, triethylene glycol dimethacrylate, diethylene glycol dimethacrylate, glycerol dimethacrylate, hydroxypropyl methacrylate, 2-hydroxyethyl methacrylate, 2-tert-butyl amino ethyl methacrylate, dimethylaminopropyl methacrylate, 2-dimethylaminoethyl methacrylate, hydroxypropyl acrylate, trimethylolpropane trimethacrylate, and a 2-acrylamido-2-methylpropane sulfonic acid derivative.
[0042] In another embodiment, the superabsorbent polymer is a copolymer of acrylamide and an acrylic acid derivative.
[0043] In another embodiment, the superabsorbent polymer is a polyacrylate/polyacrylamide copolymer.
[0044] In another embodiment, the superabsorbent polymer is a polyacrylamide.
[0045] In another embodiment, the superabsorbent polymer is a polyacrylate.
[0046] In another embodiment, the superabsorbent polymer is a guar gum.
[0047] In another embodiment, the superabsorbent polymer is cross-linked.
[0048] In another embodiment, the superabsorbent polymer is cross-linked with an oil.
[0049] In another embodiment, the superabsorbent polymer is cross-linked with mineral oil.
[0050] In another embodiment, the superabsorbent polymer is formulated as an emulsion.
[0051] In another embodiment, the emulsion comprises water and an oil.
[0052] In another embodiment, the oil is mineral oil.
[0053] In another embodiment, the emulsion comprises water, oil, and superabsorbent polymer cross-linked with mineral oil.
[0054] In another embodiment, the superabsorbent polymer is formulated as a paste.
[0055] In another embodiment, the paste comprises oil and water.
[0056] In another embodiment, the oil is mineral oil.
[0057] In another embodiment, the paste comprises water, oil, and superabsorbent polymer cross-linked with mineral oil.
[0058] In another embodiment, the polymer-based heat absorbing material is NOCHAR's P215branmd heat absorbing material.
[0059] It will be appreciated that all permitted combinations of the above embodiments, along with other embodiments described elsewhere herein, are contemplated as additional embodiments of the present invention. IV. Brief Description of Drawings
[0060] Figure 1A is a side elevational view of a shipping container of the present invention;
[0061] Figure 1B is a sectional view taken along lines 1B-1B of Figure 1A;
[0062] Figure 1C is a sectional view, similar to Figure 1B except that battery cards are shown inside the container;
[0063] Figure 1D is a top view of the shipping container shown in Figure 1A;
[0064] Figure 2A is a top view of the splitting member that includes a plurality of cells in which a heat absorbing material of the present invention is received;
[0065] Figure 2B is a sectional view taken along lines 2B-2B of Figure 2A;
[0066] Figure 2C is a sectional view, generally similar to Figure 2B of the thermal barrier, in which the inner and outer panel members are joined together to form a cavity of heat receiving material in which the splitting member and heat absorption are contained;
[0067] Figure 3 is a schematic view illustrating the molecular constitution of an outer layer of the container;
[0068] Figure 4 is a schematic view of a split member of the present invention showing the heat absorbing material contained within some of the cells;
[0069] Figure 5 is a schematic cross-sectional view of a panel of a container of an embodiment of the present invention;
[0070] Figure 6 is an end view of the first alternative embodiment of the shipping container of the present invention;
[0071] Figure 7 is a front view of the alternate embodiment of the present invention shown in Figure 6;
[0072] Figure 8 is a top view of the alternative container embodiment shown in Figure 6; and
[0073] Figure 9 is a sectional view taken along the upper left corner of Figure 7.
[0074] Figure 9 is a sectional view taken along lines 9-9 of Figure 7. V. Description of Illustrative Modalities
[0075] In order to promote an understanding of the principles of the present invention, reference will now be made to the embodiments illustrated in the drawings and specific language will be used to describe the same. However, it should be understood that no limitation on the scope of the present invention is thus intended. Any of said additional changes and modifications to the devices illustrated, and said additional applications of the principles of the present invention as illustrated herein are contemplated as would normally occur to those skilled in the art to which the present invention pertains.
[0076] As best shown in the figures, a shipping container 10 is configured to transport thermally active materials, such as battery cases 12 for batteries 14. Although thermal activity can have a wide range of both heating and cooling functionality, the The main thermally active materials for which the shipping container 10 of the present invention is designed are thermally active materials such as batteries 14, and especially lithium batteries and lithium-ion batteries (collectively "lithium batteries" herein) that have the propensity (although rare) to ignite, and engage in thermal runaways as discussed above. Lithium batteries, when they burn, ignite at a temperature that is sufficient to cause other batteries to ignite, which includes batteries in known adjacent shipping containers.
[0077] The transport container 10 of the present invention is designed to provide the thermal barrier that will prevent thermally active materials, such as burning batteries, from generating sufficient heat in the environment E of the transport container 10 to cause the containers to burn. adjacent transport containers 10, and materials adjacent to the particular transport container 10 in which the burning batteries are contained.
[0078] Transport container 10 includes a plurality of framing panels 16 that define an inner container 18 that is configured to receive thermally active batteries 14.
[0079] The structuring panels 16 also include an exterior, such as the exterior surface 20 which is disposed adjacent an environment E, in which the shipping container 10 is disposed. Typically, environment E will comprise the cargo compartment of a transport vehicle, such as a truck, aircraft or ship. Alternatively, environment E may comprise an interior space of a larger container such that the shipping container 10 comprises a "container within a container", if such an arrangement is believed to be desirable.
[0080] A thermal barrier member 26 is provided for placement between the thermally active batteries 14 and the environment E to which the transport container 10 is disposed. The thermal barrier member 26 includes an inner thermal barrier panel 28, and an outer thermal barrier panel 32. The inner thermal panel 28 and the outer thermal panel 32 define a heat-absorbing material receiving cavity 34 within the which a flowable polymer heat absorbing material 36 can be arranged. The nature and composition of the flowable polymer heat absorbing material 36 will be described in more detail below.
[0081] Preferably, the polymer based heat absorbing material is a flowable slurry material having a generally high viscosity, such as a slurry. From a chemistry point of view, the flowable polymer must be of the type of compound referred to as a "superabsorbent" that is capable of absorbing and retaining a large amount of water in an emulsion.
[0082] The flowable polymer based on heat absorbing material 36 is disposed within the cavity of heat absorbing material 34. The thermal barrier 26 is configured to substantially surround and enclose the thermally active batteries 14 to reduce the passage of thermal energy between the interior 18 of the transport container 10 in which the batteries 14 are arranged, and the environment E in which the transport container 10 is arranged.
[0083] The shipping container 10 includes a structural portion that includes a plurality of structuring panels 16. In the illustrated embodiment, the shipping container 10 has a configuration that is generally rectangular and cuboid, and that is similarly designed to a box designed to hold a typewriter paper case. In particular, the structural portion of the shipping container includes a base portion 42 and a lid portion 44. The base portion 42 includes four vertical side walls that include the first side wall 46, second side wall 48, third wall 50 and fourth side wall 52. A generally horizontally disposed button or base wall 54 has four edges, each of which is connected to one of the four side walls 46 - 52 respectively.
[0084] Each of the four side walls 46, 48, 50, 52 includes first and second side edges which are coupled to adjacent side walls, and a bottom edge which is connected to the base wall 54. Depending on the particular construction of the portion of base 42, side walls 46-52 and base wall 54 may be unitarily formed as they are in a cardboard box, embossed or vacuum formed plastic container; or alternatively, it may comprise separable panels of cardboard, lumber, metal plate or some other material that is joined along their respective side edges.
[0085] The lid member 44 is formed generally similar to a base portion 44, except that it has a relatively longer width and length, and a relatively shorter sidewall portion. The lid includes a horizontally arranged top or wall panel 58 which has four edges. The first 60, second 62, third (not shown) and fourth 66 side wall flaps each include an edge that is coupled to the side edge of the top panel 58. The side wall flaps 60-66 extend in a plane that is generally perpendicular to the plane of the horizontally arranged top wall 58, and extends downward a sufficient distance so that when the cover 44 is attached to the base 42, the lower ends of the flap members 60-66 overlap to the upper portions of the side wall portions 46-52 of the base member 42.
[0086] Thermal barrier member 24 includes cover portion 70 which is formed separately from the main body of thermal barrier 24. Cover portion 70 is formed to be generally identical to the remainder of thermal barrier 24, and is arranged along the inner surface of the side wall 60, 66 and the horizontally arranged top wall 58 of the lid portion 44, so that when the lid 44 is engaged with the base 42, combustible materials such as batteries 14 are disposed within the area battery receiving interior 18 of container 10, combustible materials such as batteries 14 are completely surrounded and enclosed by a thermal barrier 24.
[0087] In a preferred embodiment, the cover 42 is sized so that a small gap exists between the four vertical wall flaps 58 (not shown), 64, 66 and the four side walls 46-52 of the base member 44. The small gap allows a certain amount of gas to escape or vent from the interior cavity 18 while still allowing the lid 44 to be secured to the base 42 and side walls.
[0088] Preferably, some type of locking mechanism is provided to help secure the cover 44 to the base 42. The locking mechanism may comprise any of a variety of locking mechanisms, from conventional latches or latches to securing members. that surround the base 42 and the lid 44, similar to fasteners that are employed in writing paper cases.
[0089] In the case of combustion of a lithium battery, a pressure pulse may be given when the battery explodes inside the interior 18. The gas and pressure created by said pressure pulse are preferably allowed to escape from the container 10 so as to ensure that the container 10 is not compromised by the pressure pulse.
[0090] In one embodiment of the present invention, the base 42 and cover 44 are manufactured from cardboard. Cardboard is an engineered wood product that is typically made from wood chips, sawdust shavings or even sawdust and a synthetic resin or other suitable binder that is pressed and extruded. In one form, the ligand is configured to absorb water molecules.
[0091] Figure 3 illustrates a small segment of cardboard of the type that can be used in the container 10 of the present invention. The cardboard segment 22 is shown including a first retardant which is infused into the cardboard. The flame retardant 76 preferably comprises a polymer based heat absorbing material which is similar to the polymer based heat absorbing material which is used in a thermal barrier 24 and which is discussed in more detail below.
[0092] The first retarding heat absorbing polymer-based material 76 is infused into the cardboard 22, which includes a plurality of cardboard molecules 74 that have been infused with the plurality of cardboard molecules 72 that have been infused with a plurality of polymer based on heat absorbing material molecules 74.
[0093] In a preferred form as described in more detail below, the heat absorbing material is polymer based, is non-toxic, and is a non-hazardous polymer heat absorbing material that is designed for natural fiber materials unsealed and products such as cardboard 22. The preferred flame retardant 76 is described in more detail below, and is available from NOCHAR, Inc., under the trademark NOCHAR's fire preventer ("NFP"). NFP can be applied to cardboard 22 by spray, curtain coating, thermal immersion, vacuum chamber, roll coating or embedding.
[0094] NFP is a water soluble product that uses water as a vehicle to penetrate the cardboard 22. The water is then dried or stripped leaving the current heat absorbing material 76 in place within the cardboard 22.
[0095] As will be described in more detail below as well, NFP raises the first safety issue of treated materials and products by increasing the temperature and amount of heat input kilocalories required for ignition, which reduces the coefficient of ignition. heat release after ignition, and reducing the scattering coefficient of the flame.
[0096] NFP purchased by NOCHAR, Inc., can be added to bonding agents, adhesives and sealants.
[0097] The heat barrier member 24 of the present invention is shown in the figure as including a base portion 27, which lines the base 42 of the container 10, and the lid portion 29, which lines the lid.
[0098] Alternatively, the thermal barrier 24 may comprise a unitary bag-shaped member which is disposed in the container, which includes a cavity 18 therein within which the cards 40 of heat-combustible materials 14 may be disposed.
[0099] Importantly, the thermal barrier 24 must be designed so that it encloses or encompasses combustible materials such as batteries 14. Additionally, in the embodiment shown in figures 1 and 2, the thermal barrier 24 must include a member of pressure release, which may comprise a traditional pressure release valve or a space as described above so that the pressure rise caused by combustion or other thermal activity may be vented from the inside 18 of the container to the outside of the container.
[00100] The shipping container 10 includes an inner thermal barrier panel 28 which is coupled to the outer thermal barrier panel 32 to form a heat-absorbing material receiving cavity 34. An outer thermal barrier panel and panel of inner thermal barrier 28, 32 shall be produced from a flame resistant material capable of absorbing or resisting high temperatures without being compromised or melting. Additionally, the material from which the interior panels 28 and 32 are produced must be designed to be non-combustible, and strong enough to securely hold the heat-absorbing thermal barrier material contained within the cavity 34 without cracking, tearing or similar.
[00101] An example of a material that can work well in said situation is a thin aluminum foil material.
[00102] When designing materials for the transport container 10 and the thermal barrier 24, a balance of qualities and characteristics is sought. As shipping costs are often calculated as a function of weight, it is beneficial to choose the lightest weight materials possible in order to save on shipping costs. On the other hand, it is important to have a shipping container that is robust enough to withstand the rough treatment that shipping containers often receive during transit. Preferably, the shipping container can be robust enough that it can be reused on multiple occasions.
[00103] As discussed in more detail below, a preferred thermal barrier material comprises a paste in terms of consistency. As a slurry is a flowable material, the materials from which the outer panels 28, 32 are produced must be robust enough that it will not be easily tampered with, as tampering can causing the heat absorbing flowable material to leak out of the inner receiving cavity 34 of the thermal barrier. As such, a thin sheet, while saving weight, may not be robust enough to easily avoid said violations. Therefore, a thickened sheet or laminate of a metal material such as aluminum is likely to be more preferred than the use of a sheet.
[00104] A split member 38 is disposed within the internal heat absorbing material receiving cavity 34 of the thermal barrier. The split member, as shown in Figure 2, comprises a lattice-shaped working member of a generally rigid material such as a metal or plastic that includes a series of openings or cells 80 that have hollow interiors within which the polymer with flow capacity and heat absorption 36 can be arranged. The purpose of the splitting member 38 is to better disperse the heat absorbing polymer 36 contained within the cells over the entire surface area of the thermal barrier. As will be seen, the flowable nature of the thermal barrier material is likely to result in aggregation and collection of a heat absorbing polymer based material under the influence of gravity in the lower portions of cavity 34. By employing the division 38, a paste-like heat absorbing material will be retained and dispersed throughout the area of the thermal barrier.
[00105] As shown in Figure 1C, a plurality of thermal barrier segments may be used, such as thermal barrier segments 84 and 88 which are disposed adjacent side walls 48, 52 of structural member 16, and barrier panel. 88 which is disposed adjacent the base panel 54 of the structural member 16. Additionally, a base panel segment 90 may be provided which is positioned adjacent the underside of the inner surface of the top panel 58.
[00106] A major factor influencing the shape of the various thermal barrier segments 84-90 is the stiffness (or lack thereof) of the split member 38. For example, if it is desired to use a split member configured flat and in 38, the barrier panel 24 itself is likely to adopt a flat or mat-shaped configuration. However, if a formed or more flexible split member 38 is used, a heat barrier 24 can be constructed of any shape into which split member 38 can be folded, molded or otherwise configured.
[00107] To create the top panel of the thermal barrier member 90, a generally flat split member 38 may be adopted that has been sized and configured to have an overall size and shape similar to the size and shape of the top panel 58 To said generally flatly arranged splitting member 38, the flap splitting members can then be attached to the main splitting member at 90 degrees thereto, so that the flap splitting members can be disposed adjacent the flap portions. flaps 62, 66 of the lid member 58.
[00108] The various cells within the splitting member 38 can then be filled with the heat-absorbing flow-capable material.
[00109] In operation, the heat-absorbing paste with flow capability helps resist the spread of fire to adjacent containers by absorbing heat generated by a fire inside 18 of container 10. As such, although the temperature inside the container may be above 953 degrees of the lithium battery combustion threshold temperature, the outside temperature of the container 10 will be significantly less than 950 degrees.
[00110] Within the interior 18 of the container, the intense heat generated by the burning batteries, which burn well above 1100 degrees, will likely ignite adjacent batteries within the interior 18 of the container 10. As such, a fire in a single battery can lead to a thermal runaway which causes other batteries within the interior 18 of the container 10 to also catch fire. This fire will provide heat and pressure, especially when the battery explodes. As discussed above, the pressure will be vented by a space through which the gas can pass that is formed in the construction of the container, or even by a traditional pressure release valve that allows the gas to pass if the pressure within the interior space exceeds. a predetermined threshold.
[00111] Regardless of the high heat generated within the interior 18 of the container 100, the exterior environment E of the container 10 will not rise above a predetermined threshold for combustion of the batteries in adjacent containers, because the heat-absorbing material is capable of to absorb the heat generated by the burning batteries 14 within the transport container 10. As such, said thermal blockage by the heat absorbing material 36 serves to effectively contain fire and excessive heat within the interior 18 of the container 10, and prevent the outside environment AND of the container from becoming too hot.
[00112] In a preferred embodiment of the present invention, the device 10 may be designed so that the heat-absorbing material is sufficient in heat-absorbing and heat-blocking capacity to ensure that the outer atmosphere of the container does not rise. above 953 degrees of threshold point of combustion of lithium batteries in adjacent containers, when lithium batteries within the interior 18 of the container catch fire.
[00113] Although cell 80 in Figure 2 is shown to be generated rectangular in configuration, it will be seen that cells 80 can take a variety of shapes depending on how the cells are formed in the splitting member.
[00114] It is important that the covering materials of the thermal barrier 28, 32 are produced from the flame resistant material, in case they catch fire, the heat generated by the fire of the barrier panel 28, 30, can cause the outside temperatures of the environment E of the container 10 also rise significantly. Additionally, if the heat barrier panels 28, 30 catch fire, the heat from the fire thus created may be sufficient to cause the container framing panels 16 to catch fire, thus allowing heat to reach adjacent containers. . Arguably, said heat can be intense enough to cause nearby containers to catch fire, thereby igniting nearby batteries therein causing additional thermal runaways.
[00115] During initial testing of container 10, unexpected results were obtained regarding the ability of container 10 to contain fire. Li-ion batteries have been reported to ignite at about (953o F) and can reach temperatures exceeding (1100o F) during combustion. During testing of container 10 described herein, flames exceeding (1400°F) were introduced into internal cavity 18 and container 10 was sealed for 20 minutes, 40 minutes, and 60 minutes while the fire was allowed to burn. In particular, flares, which do not require oxygen to burn, were introduced into the inner cavity 18.
[00116] After the tests were conducted, although there were burn marks on the layers of fire resistant material 28, 32 the thermal barrier 24 was able to prohibit the combustion of the outer panel members 16 of the container 10. As such, all flames from the fire were contained within the interior cavity of the container 10. Thus, the container 10 described here is capable of preventing the fire from the lithium ion batteries within the internal cavity 14 from spreading beyond the container 10 thereby increasing the transport safety of lithium-ion batteries.
[00117] An alternative embodiment of the shipping container 100 is shown in Figures 6-9. The shipping container 100 has a configuration that is relatively reminiscent of a steam trunk, or shipping container of the type used by roadside bands to house their amplifiers, drums and other musical instruments during transport. Preferably, shipping container 100 includes a plurality of structuring panels that are produced from a strong, yet lightweight, fire-resistant metal material such as aluminum or titanium. Alternatively, the panels can be produced from a fire resistant plastic.
[00118] Although the container 100 can be produced in any size, in a more preferred embodiment the container has a square cross section over a horizontal plane and a rectangular cross section over a vertical plane so that the width and length of the container ( without metal feet or top limbs) of approximately 390 centimeters, and the height is approximately 265 centimeters.
[00119] The alternative embodiment of the container 100 includes a base member 103 which is detachably coupled to the lid 105. The lid 105 is removable from the base member 103 so that not only the thermal barrier (not shown) , but also load such as batteries 14 can be arranged within the hollow interior (not shown) of container 100.
[00120] As container 100 is rectangular and cuboid, it includes four side panels 106 of generally equal size, along with a base panel 103, which is generally square in configuration. Lid 105 includes a top panel 116 and four flap panels 118 which are arranged in a generally perpendicular relationship with and downwardly extending top panel 116 therefrom. An edge member may be formed at the edge of the flap panel member to engage the upper edge of the side wall of the base member 106. As shown in Figure 9, the flap panel members overlap the upper portion of the side panel, and an engaging seal 131 is provided to sealingly engage the reinforced top edge 135 of the side panel member 106.
[00121] Reinforced bottom corner members 122 are disposed at the intersection of bottom panel 104 and side panels 106. Reinforced corner members 122 also include downwardly overhanging feet 124 that help provide stable engagement with the rest of the frame. surface such as a floor or bottom container for the particular container 100.
[00122] In addition, the reinforced corner members 128 are secured to the lid at the corners where the top panel 116 meets the flap members 118. Preferably, as shown in Figure 8, the top corner panel members include an area of receiving which is designed to receive the feet 124 of a container disposed on top of the particular container to help lock the upper container onto the lid of the lower container so that it is able to resist movement.
[00123] A plurality of locking members 136 (here shown as four) are coupled to the front and rear side panel members and include a hook and loop locking mechanism to engage the cover 105 to the base 104 in a manner in which the lid and base will be connected and resist separation. Locking members 136 may be designed to lock if desired.
[00124] The first and second rods, 140, are arranged on the side panel members, and include a rod to make it easier to lift and load the container 100. The pressure release valve 142 is provided that includes a gas passage. which extends between the interior cavity of the container 100 and the environment E in which the container is arranged to prevent an over-pressure situation within the interior of the container 100 of the type that can cause the container 100 to explode. By venting pressure, such an explosion can be avoided. Additionally, a hydroscope 145 is also provided on the container 100.
[00125] In operation, the container 100 generally operates similarly to the container 10 shown in the other figures. Although not shown in the drawings, the thermal barrier, similar to the thermal barrier 24 as shown in connection with Figure 1, may be disposed within the interior of an alternative embodiment of the container 100.
[00126] Presented below is a description of the flowable polymer based heat absorbing material that is used in the thermal barrier 24 described above. Polymer based heat absorbing material
[00127] The polymer-based heat absorbing material of the present invention comprises a superabsorbent polymer (SAP). SAPs are water-absorbing materials that are capable of absorbing between about 40 and about 400 times their weight in water. Superabsorbent polymers are produced by adding to a reaction mixture of linear polymers one that forms two-dimensional and/or three-dimensional bonds between linear molecules. The effect of said cross-linking is to immobilize the linear molecules. Their affinity for water is not reduced, but now the water must be absorbed within the lattice structure. The polymer itself does nothing to prevent or quench combustion, but instead isolates and immobilizes trapped water that might otherwise either evaporate or go away from the combustion surface, in either case becoming ineffective at preventing combustion. fire.
[00128] In one embodiment, the SAP is formulated as a liquid emulsion, preferably an oil and water emulsion, more preferably a water and mineral oil emulsion. Although said emulsions are desirable in that they keep the components uniform, they can eventually separate into hydrophobic and hydrophilic layers given sufficient time without agitation. Therefore, it is advantageous to convert the emulsion to a water-containing slurry, which is not susceptible to phase separation, using high shear with additional water. It is additionally desirable to irradiate the emulsion to induce crosslinking of the SAP with the mineral oil. By varying the parameters of these processes, not only the viscosity, but also the molecular weight of the resulting material can be customized. An example of said preferred material is NOCHAR's P215TM. In said embodiment, it will be appreciated that the material may include other crosslinking agents in addition to mineral oil.
[00129] The resulting water-containing paste is then used to insulate the box described here. In the event of a fire in the internal lithium battery, the paste works to effectively and efficiently extract heat out of the system by virtue of the high heat capacity of the water in the paste. The result is that the fire is contained within the box and extinguished. In a load situation, this ensures that the fire does not spread to the adjacent load and ultimately to the vehicle itself.
[00130] Examples of superabsorbent polymers include cross-linked polyacrylates and their derivatives, such as polyacrylamide and polyacrylate salts (i.e., sodium polyacrylate or potassium polyacrylate), polyacrylate/polyacrylamides copolymer, and starch graft polymers. . Polyacrylate salts such as sodium polyacrylate or potassium polyacrylate can absorb up to about 500 times their weight in water, or more. However, because they are salts, their absorption capacity is largely dependent on the impurities in the water. For example, "hard water", or water with a relatively high concentration of calcium or magnesium ions, reduces the absorption capacity of potassium polyacrylate because the ions break the bond between the polymer and the water. Polyacrylamide is not as affected by hard water, but it does not have as high an absorption capacity as polyacrylate salts. Polyacrylamide is known to be able to absorb between about 20 times and about 400 times its weight in water. However, even at absorption capacities as low as 100 times its weight in water, polyacrylamide can still absorb enough water to be an effective flame retardant.
[00131] In other embodiments, the superabsorbent polymer is a polymer of hydrophilic monomers, such as acrylamide, acrylic acid derivative, maleic acid anhydride, itaconic acid, 2-hydroxy ethyl acrylate, polyethylene glycol dimethacrylate, allyl methacrylate, tetraethylene glycol dimethacrylate, triethylene glycol dimethacrylate, diethylene glycol dimethacrylate, glycerol dimethacrylate, hydroxypropyl methacrylate, 2-hydroxyethyl methacrylate, 2-tert-butylaminoethyl methacrylate, dimethylaminopropyl methacrylate, 2-dimethylaminoethyl methacrylate , hydroxypropyl acrylate, trimethylolpropane trimethacrylate, or 2-acrylamido-2-methylpropane sulfonic acid derivatives, as described in US patent publication no. 2009/0069496 A1 (p. 2 to 18-19). The superabsorbent polymer may also be a copolymer of acrylamide and acrylic acid derivatives or a terpolymer of a salt of acrylate, acrylamide, and a salt of 2-acrylamido-2-methylpropane sulfonic acid (AMPS). The salts may in general be any monovalent salts, such as the sodium, potassium or ammonia salts.
[00132] Berg et al., in US Patent No. 5,397,626, also describes suitable superabsorbent polymers (see column 6, line 47 to column 8, line 53). As described by Berg et al., SAPs include cross-linked polymers prepared from monomers that contain polymerizable, unsaturated acid, which include olefinically unsaturated acids and anhydrides that contain at least one carbon to the olefinic carbon double bond. More specifically, said monomers include olefinically unsaturated carboxylic acids and acid anhydrides, olefinically unsaturated sulfonic acids, and mixtures thereof.
[00133] Some non-acidic monomers can also be used to prepare the precursor particles here. Said non-acidic monomers may include, for example, the water-soluble or water-dispersible esters of acid-containing monomers as well as monomers that do not contain any carboxyl groups or sulfonic acid. Optional non-acidic monomers may thus include monomers that contain the following types of functional groups: carboxylic acid or sulfonic acid esters, hydroxyl groups, amide groups, amino groups, nitrile groups, and the quaternary ammonium salt groups. Said non-acidic monomers are well known materials and are described in more detail, for example, in US Patent No. 4,076,663 and US Patent No. 4,062,817.
[00134] Olefinically unsaturated carboxylic acid and carboxylic acid anhydride monomers include the acrylic acids typified by acrylic acid itself, methacrylic acid, ethacrylic acid, alpha-chloroacrylic acid, alpha-cyanoacrylic acid, beta methyl acrylic acid (crotonic acid) , alpha-phenyl acrylic acid, beta-acryloxy propionic acid, sorbic acid, alpha-chloro sorbic acid, angelic acid, cinnamic acid, p-chloro cinnamic acid, beta-steryl acrylic acid, itaconic acid, citraconic acid, mesaconic acid , glutaconic acid, aconitic acid, maleic acid, fumaric acid, tricarboxyethylene and maleic acid anhydride.
[00135] Some superabsorbent polymer materials for use in the present invention include a carboxyl group. Examples of said polymers include hydrolyzed starch-acrylonitrile graft copolymers, partially neutralized starch-acrylonitrile graft copolymers, acrylic acid-starch graft copolymers, acrylic acid-partially neutralized starch graft copolymers, acrylic ester-amido acetate copolymers. saponified vinyl, hydrolyzed acrylonitrile or acrylamide copolymers, partially crosslinked products of any of the aforementioned copolymers, partially or fully neutralized polyacrylic acid, and partially crosslinked and partially neutralized polyacrylic acid products. Said polymers can be used independently or in the form of copolymers formed from a mixture of two or more of said monomers.
[00136] Some superabsorbent polymer materials are cross-linked products of partially neutralized polyacrylic acids and the amide derivatives therefrom. For example, the solid particles of SAP can comprise from about 50% to about 95%, or about 75% cross-linked neutralized polyacrylic acid, for example, poly(sodium acrylate/acrylic acid).
[00137] The polymer materials are cross-linked to an extent so that the polymer is insoluble in water. Crosslinking serves to make the polymers substantially water-insoluble and in part serves to determine the absorbency of the polymers. Suitable crosslinking agents are known in the art and include di- or polyfunctional molecules capable of crosslinking the polyacrylic acid and/or the polyacrylic acid metal salts by reaction with the acrylic or acrylate functional groups of the polymer. Said cross-linking agents include diglycidyl esters, dialcohols, and diamines. In general, the crosslinking agent should be water soluble and have reactivity with the polymer so that crosslinking occurs in a controlled manner over a temperature range of about 50°C. to about 150°C. Crosslinking Agents suitable include ethylene glycol, polyethylene glycols, polypropylene glycols, and the diglycidyl esters of (poly)ethylene glycols. One such agent is ethylene glycol diglycidyl ether (EGDGE), a water-soluble diglycidyl ether. Additional crosslinking agents are described in EPO 450 923 A2 (Nippon Shokubai Kagaku Kogyo Co.).
[00138] Erdner et al., US Patent No. 7,670,515, also describes suitable superabsorbent polymers (col. 4, line 8 to col 8, line 61). As described by Erdmer et al., SAPs are generally relatively cross-linked hydrophilic polymers as discussed in US Patent Nos. 5,669,894 and 5,559,335. SAPs may differ in their chemical identity, but all SAPs are capable of absorbing and retaining amounts of aqueous fluids equivalent to many times their own weight, even under moderate pressure. For example, SAPs can absorb hundreds of times their own weight or more of distilled water.
[00139] SAPs are available from a variety of chemical firms, which include substituted and unsubstituted natural and synthetic polymers, such as the hydrolysis products of acrylonitrile and starch graft polymers, carboxymethyl cellulose, cross-linked polyacrylates, isobutylene and anhydride copolymers. cross-linked and partially neutralized maleic acid, vinyl acetate-acrylic acid copolymer saponification products, sulfonated polystyrenes, hydrolyzed polyacrylamides, polyvinyl alcohols, polyethylene oxides, polyvinylpyrrolidones, and polyacrylonitriles.
[00140] A SAP is typically neutralized at least about 25 mol %, preferably at least about 50 mol %, and generally about 70 to 80 mol %, to achieve optimal absorption. Neutralization can be achieved by neutralizing the acrylic acid monomer prior to polymerization of the monomer, or the polymer can be neutralized after the polymerization reaction is substantially complete. After polymerization and internal crosslinking of the monomer, followed by partial neutralization, e.g. 50-100 mol % neutralization, preferably 70 to 80 mol % neutralization, the polymer is subdivided, e.g. minced or cut, to a drying more efficiently, and then dried and ground to a desired particle size. The polymer can then be surface crosslinked and again dried to form the final product.
[00141] The SAP may be an acidic water-absorbing resin or a basic water-absorbing resin. Monomers useful in preparing a SAP are described in US Patent No. 5,149,750 and WO 01/68156, each of which is incorporated herein by reference. In some embodiment, the SAP comprises an acidic or basic water absorbing resin neutralized to about 25% to about 100%, i.e., it has a degree of neutralization (DN) of from about 25 to about 100.
[00142] SAP can be anionic (an acidic water-absorbing resin) or cationic (a basic water-absorbing resin) in nature. Anionic SAPs are based on an acidic water-absorbing resin. Anionic SAPs, whether strongly acidic or weakly acidic, can be any resin that acts as a SAP in its neutralized form. Acidic resins typically contain a plurality of carboxylic acid, sulfonic acid, phosphonic acid, phosphoric acid, and/or sulfuric acid moieties.
[00143] In some embodiment, the SAP is an acidic water-absorbing resin neutralized 25% to 100%. The acidic water-absorbing resin can be a single resin or a mixture of resins. The acidic resin can be a homopolymer or a copolymer. The identity of the acidic water-absorbing resin is not limited as long as the resin is capable of swelling and absorbing at least ten times its weight in water when in a neutralized form.
[00144] The acidic water-absorbing resin is typically a weakly crosslinked acrylic resin, such as weakly crosslinked poly(acrylic acid). The weakly cross-linked acidic resin is typically prepared by polymerizing an acidic monomer that contains an acyl moiety, e.g. acrylic acid, or a moiety capable of providing an acid group, i.e. acrylonitrile, in the presence of an internally cross-linked monomer, i.e. that is, a polyfuctional organic compound. The acidic resin may contain other copolymerizable units, i.e. other monoethylenically unsaturated comonomers, well known in the art, provided that the polymer is substantially, i.e. at least 10%, at least 25%, at least 50%, at least 75 %, or up to 100% acidic monomer units.
[00145] Ethylenically unsaturated carboxylic acid and carboxylic acid anhydride monomers useful in the acidic water absorbing resin include acrylic acid, methacrylic acid, ethacrylic acid, a-chloroacrylic acid, a-cyanoacrylic acid, e-methylacrylic acid (crotonic acid ), a-phenylacrylic acid, e-acryloxy-propionic acid, sorbic acid, a-chlorosorbic acid, angelic acid, cinnamic acid, p-chlorocinnamic acid, e-stearylacrylic acid, itaconic acid, citraconic acid, mesaconic acid, glutaconic acid, aconitic acid, maleic acid, furmaric acid, tricarboxyethylene, and maleic anhydride. Acrylic acid is an ethylenically unsaturated carboxylic acid for the preparation of SAP.
[00146] Ethylenically unsaturated sulfonic acid monomers include aliphatic and aromatic sulfonic acids, such as vinyl sulfonic acid, allyl sulfonic acid, toluene vinyl sulfonic acid, styrene sulfonic acid, acrylic and methacrylic sulfonic acids, such as acrylate sulfoethyl, sulfoethyl methacrylate, sulfopropyl acrylate, sulfopropyl methacrylate, 2-hydroxy-3-methacryloxypropyl sulfonic acid, and 2-acrylamido-2-methyl-propane sulfonic acid. Acidic phosphate-containing resins are prepared by homopolymerizing or copolymerizing ethylenically unsaturated monomers that contain a phosphoric acid moiety, such as methacryloxy ethyl phosphate. An extensive list of suitable SAP forming monomers can be found in US Patent No. 4,076,663.
[00147] The anionic SAPs can be, for example, a poly(acrylic acid), a hydrolyzed starch-acrylonitrile graft copolymer, a starch-acrylic acid graft copolymer, an acrylic acid graft copolymer, saponified vinyl acetate , a hydrolyzed acrylonitrile copolymer, a hydrolyzed acrylamide copolymer, an ethylene-maleic anhydride copolymer, an isobutylene-maleic anhydride copolymer, a poly(vinyl sulfonic acid), a poly(vinyl phosphonic acid), a poly(vinyl phosphonic acid) (vinylphosphoric), a poly(vinylsulfuric acid), a sulfonated polystyrene, and mixtures thereof. An anionic SAP is a poly(acrylic acid).
[00148] The polymerization of acidic monomers, and co-polymerizable monomers, if present, is most commonly performed by free radical processes in the presence of an internal polyfunctional crosslinking monomer. The acidic resins are cross-linked to a sufficient extent so that the polymer is insoluble in water. Cross-linking renders acidic resins substantially insoluble in water, and in part, serves to determine the absorptive capacity of resins. For use in absorption applications, an acidic resin is lightly crosslinked, that is, it has a crosslink density of less than about 20%, less than about 10%, or about 0.01% to about 7%. An internally crosslinked monomer can be used in an amount of less than about 7% by weight, and typically from about 0.1% by weight to about 5% by weight, based on the total weight of the monomers.
[00149] Examples of internally cross-linked monomers include, but are not limited to, the polyacrylic (or polymethacrylic) acid esters represented by the following formula (I),
where x is ethylene, propylene, trimethylene, cyclohexyl, hexamethylene, 2-hydroxypropylene,

wherein nor, independently, are an integer from 5 to 40, and k is 1 or 2; and bisacrylamides, represented by the following formula (II),
where I is 2 or 3.
[00150] Compounds of formula (I) are prepared by reacting polyols, such as ethylene glycol, propylene glycol, trimethylolpropane, 1,6-hexanediol, glycerin, pentaerythritol, polyethylene glycol, or polypropylene glycol, with acrylic acid or meth acid. -acrylic. Compounds of formula (II) are obtained by reacting polyalkylene polyamines, such as diethylenetriamine and triethylenetetramine, with acrylic acid. Specific cross-linking monomers are described in US Patent No. 6,222,091. Examples of crosslinking agents are triallyl pentaerythritol ether, pentaerythritol triacrylate, N,N'-methylenebisacrylamide, N,N'-methylenebismethacrylamide, ethylene glycol dimethacrylate, and trimethylolpropane triacrylate.
[00151] Analogs of acidic resin, a basic water-absorbing resin, i.e., cationic SAP, useful in the present SAP clay particles may be a strong or weak basic water-absorbing resin. The basic water-absorbing resin can be a single resin or a mixture of resins. The basic resin can be a homopolymer or a copolymer. The identity of the base resin is not limited as long as the base resin is capable of swelling and absorbing at least 10 times its weight in water when in a charged form. The weak basic resin may be present in its cationic form, i.e. about 25% to 100% of the basic fractions, eg amino groups, are present in a charged form. Strong basic resins are typically present in the hydroxide (OH) or bicarbonate (HCO3) form.
[00152] The basic water-absorbing resin is typically a lightly cross-linked resin, such as poly(vinylamine) or poly(dialkylaminoalkyl(meth)acrylamide). The basic resin can also be, for example, a lightly cross-linked polyethyleneimine, a poly(allylamine), a poly(allylguanidine), a poly(dimethyldiallylammonium hydroxide), a quaternized polystyrene derivative, a guanidine-modified polystyrene , a quaternized poly((meth)acrylamide) or ester analogue. See US Patent No. 6,235,965. The lightly cross-linked water-absorbing resin may contain other copolymerizable units and is cross-linked using an internally cross-linked monomer, as determined above with respect to the acidic water-absorbing resin. Examples of basic resins include a poly(vinylamine), polyethyleneimine, poly(vinylguanidine), poly(dimethylaminoethylacrylamide) (poly(DAEA)), and poly(dimethylaminopropyl methacrylamide) (poly-(DMAPMA)).
[00153] A basic water-absorbing resin used in the present SAP typically contains an amino group or a guanidino group. Thus, a water-soluble base resin can also be crosslinked in solution by suspending or dissolving an uncrosslinked base resin in an aqueous or alcoholic medium, then adding a di- or polyfunctional group capable of crosslinking the base resin by reaction with the groups amino of the basic resin. Said cross-linking agents are described in US Patent No. 6,235,965. Crosslinking agents are also described in US Patent No. 5,085,787, and in EP 450,923. Examples of crosslinking agents are ethylene glycol diglycidyl ether (EGDGE), a water-soluble diglycidyl ether, and a dibromoalkane, a soluble compound. in alcohol.
[00154] Copolymerizable monomers for introduction into an acidic resin or a basic resin include, but are not limited to, ethylene, propylene, isobutylene, C1-C4 alkyl acrylates and methacrylates, vinyl acetate, methyl vinyl ether, and styrenic compounds having the formula:
wherein R represents hydrogen or a C1-C6 alkyl group, and wherein the phenyl ring is optionally substituted with one to four C1-C4 alkyl or hydroxy groups.
[00155] Suitable C1-C4 alkyl acrylates include, but are not limited to, methyl acrylate, ethyl acrylate, isopropyl acrylate, n-propyl acrylate, n-butyl acrylate, and the like, and mixtures thereof. Suitable C1-C4 alkyl methacrylates include, but are not limited to, methyl methacrylate, ethyl methacrylate, isopropyl methacrylate, n-propyl methacrylate, n-butyl methacrylate, and the like, and mixtures thereof or with alkyl acrylate C1-C4. Suitable styrenic compounds include, but are not limited to, styrene, α-methylstyrene, p-methylstyrene, t-butyl styrene, and the like, and mixtures thereof or with C1C4 alkyl acrylates and/or methacrylates.
[00156] Any polymerization initiator known for use in preparing the SAPs may be used. Examples of useful initiators are redox and thermal initiators, such as those described in US Patent No. 6,359,049. Redox and thermal initiators can be used singly or in a suitable combination. The specific initiators are a redox initiator comprising ammonium persulfate and sodium hydrogen sulfite, and azo initiators, such as azobisisobutyronitrile and 2,2'-azobis(2-amidinopropane) dihydrochloride, commercially offered under the tradename registered V-50 offered by Wako Chemicals USA, Inc., Richmond, Virginia. The initiator is typically used in an amount, calculated as solids, of from about 0.1% to about 10%, based on the weight of the acrylic acid monomer, or from about 0.5% to about 5%, with based on monomer weight. Depending on the amount and type of initiator, the initiator optionally can be used together with isopropyl alcohol, an alkyl mercaptan, or other chain transfer agent to control the molecular weight of the poly(acrylic acid).
[00157] Ultraviolet (UV) light can also be used to effect acrylic acid polymerization. Ultraviolet light can be used in conjunction with a redox initiator and/or a free radical initiator. When ultraviolet light is used in the polymerization step, a photoinitiator is also added to the reaction mixture in an amount well known to those skilled in the art. Suitable photoinitiators include, but are not limited to, 2-hydroxy-1-[4-(hydroxyethioxy)phenyl]-2-methyl-1-propanone, which is commercially available from Ciba Additives of Hawthorne, NI, as IRGACURE 2959 , and 2-hydroxy-2-methyl-1-phenyl-1-propanone, which is also commercially available from Ciba Additives as DAROCUR 1173.
[00158] Useful industrial processes for SAP component preparation include all processes commonly used to synthesize SAPs, as described, for example, in Chapter 3 of "Modern Superabsorbent Polymer Technology," FL Buchholz and AT Graham, Wiley- VCH (1998). A suitable process for acrylic acid polymerization is aqueous solution polymerization, wherein an aqueous solution containing acrylic acid and polymerization initiator is subjected to a polymerization reaction and a crosslinking reaction by the addition of a monomer. of internal crosslinking, such as methylenebisacrylamide.
[00159] While various embodiments have been described as having particular features and/or combinations of the components, other embodiments are possible having a combination of any features and/or components from any of the embodiments as discussed above. As used in the present report, the singular forms "a," "a," and "the" include plural referents unless the context clearly dictates otherwise.
[00160] Although the present invention has been illustrated and described in detail in the drawings and in the previous description, it should be considered as illustrative and not as restrictive, it being understood that all changes and modifications that fall within the spirit of the present invention are desired to be protected.

权利要求:
Claims (11)
[0001]
1. Transport container (10) configured for the transport of thermally active materials (14), the transport container (10) characterized in that it comprises: a plurality of structuring panels (16) defining an inner container (18) ) configured to receive the thermally active materials (14), and an exterior disposed adjacent an environment in which the transport container (10) is disposed, a thermal barrier member (24) for placement between the thermally active materials (14) ) and the environment in which a container is disposed, the thermal barrier including an interior thermal barrier panel (28), and an exterior thermal barrier panel (32) defining a heat-absorbing material receiving cavity (34). ), and a flowable polymer based on heat absorbing material (34) disposed within the heat absorbing material receiving cavity (34), wherein the thermal barrier is configured to surround the materials. thermally active materials (14) to reduce the passage of thermal energy between the thermally active materials (14) and the environment in which the transport container (10) is disposed, wherein the polymer based heat absorbing material (34) ) comprises a superabsorbent polymer which is hydrated with water, wherein the superabsorbent polymer is a polyacrylate/polyacrylamide copolymer.
[0002]
2. Transport container (10) configured for transporting thermally active materials (14), the transport container (10) characterized in that it comprises: a plurality of structuring panels (16) defining an inner container (18) ) configured to receive the thermally active materials (14), and an exterior disposed adjacent an environment in which the transport container (10) is disposed, a thermal barrier member (24) for placement between the thermally active materials (14) ) and the environment in which a container is disposed, the thermal barrier including an interior thermal barrier panel (28), and an exterior thermal barrier panel (32) defining a heat-absorbing material receiving cavity (34). ), and a flowable polymer based on heat absorbing material (34) disposed within the heat absorbing material receiving cavity (34), wherein the thermal barrier is configured to surround the materials. thermally active materials (14) to reduce the passage of thermal energy between the thermally active materials (14) and the environment in which the transport container (10) is disposed, wherein the polymer based heat absorbing material (34) ) comprises a superabsorbent polymer which is hydrated with water, wherein the superabsorbent polymer is cross-linked with an oil.
[0003]
3. Transport container (10), according to claim 2, characterized in that the oil is a mineral oil.
[0004]
4. Transport container (10) configured to transport thermally active materials (14), the transport container (10) characterized in that it comprises: a plurality of structuring panels (16) defining an inner container (18) configured to receive the thermally active materials (14), and an exterior disposed adjacent an environment in which the transport container (10) is disposed, a thermal barrier member (24) for placement between the thermally active materials (14) and the environment in which a container is disposed, the thermal barrier including an inner thermal barrier panel (28), and an outer thermal barrier panel (32) defining a heat absorbing material receiving cavity (34), and a flowable polymer based on heat absorbing material (34) disposed within the heat absorbing material receiving cavity (34), wherein the thermal barrier is configured to surround the materials. thermally active materials (14) to reduce the passage of thermal energy between the thermally active materials (14) and the environment in which the transport container (10) is disposed, wherein the polymer based heat absorbing material (34) ) comprises a superabsorbent polymer which is hydrated with water, wherein said superabsorbent polymer is formed as an emulsion.
[0005]
5. Transport container (10), according to claim 4, characterized in that the emulsion comprises water and oil.
[0006]
6. Transport container (10), according to claim 5, characterized in that the oil is a mineral oil.
[0007]
7. Transport container (10), according to claim 33, characterized in that said emulsion comprises water, oil and superabsorbent polymer cross-linked with mineral oil.
[0008]
8. Transport container (10) configured for the transport of thermally active materials (14), the transport container (10) characterized in that it comprises: a plurality of structuring panels (16) defining an inner container (18) ) configured to receive the thermally active materials (14), and an exterior disposed adjacent an environment in which the transport container (10) is disposed, a thermal barrier member (24) for placement between the thermally active materials (14) ) and the environment in which a container is disposed, the thermal barrier including an interior thermal barrier panel (28), and an exterior thermal barrier panel (32) defining a heat-absorbing material receiving cavity (34). ), and a flowable polymer based on heat absorbing material (34) disposed within the heat absorbing material receiving cavity (34), wherein the thermal barrier is configured to surround the materials. thermally active materials (14) to reduce the passage of thermal energy between the thermally active materials (14) and the environment in which the transport container (10) is disposed, wherein the polymer based heat absorbing material (34) ) comprises a superabsorbent polymer which is hydrated with water, wherein said superabsorbent polymer is formed into a paste.
[0009]
9. Transport container (10), according to claim 8, characterized in that the paste comprises oil and water.
[0010]
10. Transport container (10), according to claim 9, characterized in that the oil is a mineral oil.
[0011]
11. Transport container (10), according to claim 8, characterized in that the paste comprises water, oil, and a superabsorbent polymer cross-linked with mineral oil.

类似技术:

---

公开号 | 公开日 | 专利标题

---

BR112017003400B1|2022-01-11|SHIPPING CONTAINER THAT HAS A FLAME RETARDANT LAYER AND A THERMAL BLOCKING LAYER

---

CN107078232B|2021-03-26|Lithium ion battery with improved safety against combustion

---

ES2312032T3|2009-02-16|COMPOSITIONS FOR THE EXTINCTION OF FIRE AND / OR FOR THE INHIBITION OF FIRE.

---

US20170133720A1|2017-05-11|Covalently cross-linked gel electrolytes

---

Wang et al.2016|The efficiency of heptafluoropropane fire extinguishing agent on suppressing the lithium titanate battery fire

---

Liu et al.2018|Experimental study on the efficiency of dodecafluoro-2-methylpentan-3-one on suppressing lithium-ion battery fires

---

WO2006080411A1|2006-08-03|Fuel mixture for fuel cell

---

US20140224465A1|2014-08-14|Hydrophilic polymer thermal barrier system

---

CN105140427B|2019-01-08|It is a kind of to prevent lithium battery and its package burning material and preparation method

---

US20190319234A1|2019-10-17|Lithium Ion Battery Suppression System

---

US10745185B2|2020-08-18|Flame retardant shipping container

---

Li et al.2020|Full-scale experimental study on the combustion behavior of lithium ion battery pack used for electric vehicle

---

CN209544461U|2019-10-25|A kind of battery modules

---

TWI690350B|2020-04-11|System and method for battery fire extinguishing through flooding the battery

---

WO2014069022A1|2014-05-08|Automatic fire extinguisher

---

CN105552297B|2017-12-22|A kind of lithium ion battery with high security

---

KR101488058B1|2015-01-30|Secondary battery having improved safety

---

CN108232044A|2018-06-29|Battery pack and with its vehicle

---

WO2021111647A1|2021-06-10|Ignition prevention apparatus for power storage device

---

CN210331433U|2020-04-17|Energy storage battery cluster with fire control structure

---

JPWO2021064993A1|2021-11-11|Heat transport container and heat transport system

---

US20200403201A1|2020-12-24|Apparatus and method for thermal runaway propagation prevention

---

AU2021102630A4|2021-07-08|Novel high-efficiency composite fire extinguishing agent and preparation thereof

---

CN107615568B|2020-09-15|Battery pack

---

JP2010147004A|2010-07-01|Secondary battery unit

同族专利:

---

公开号 | 公开日

---

US10584829B2|2020-03-10|

---

AU2017100114A4|2017-03-02|

---

US9631773B2|2017-04-25|

---

JP2017534531A|2017-11-24|

---

CN107074431A|2017-08-18|

---

BR112017003400A2|2017-11-28|

---

JP6410244B2|2018-10-24|

---

EP3186164A1|2017-07-05|

---

MX2017002286A|2017-05-01|

---

AU2015306619B2|2017-12-07|

---

US20170146191A1|2017-05-25|

---

KR20170041764A|2017-04-17|

---

US11125390B2|2021-09-21|

---

US20190137037A1|2019-05-09|

---

KR101967075B1|2019-04-08|

---

AU2015306619A1|2017-02-16|

---

US20160091141A1|2016-03-31|

---

EP3186164A4|2018-04-18|

---

CA2957727C|2017-09-12|

---

WO2016033223A1|2016-03-03|

---

CA2957727A1|2016-03-03|

引用文献:

---

公开号 | 申请日 | 公开日 | 申请人 | 专利标题

---

---

US4059753A|1974-04-25|1977-11-22|General Electric Company|Gasket material and method of making|

---

JPS5346199B2|1975-03-27|1978-12-12|

---

US4062817A|1977-04-04|1977-12-13|The B.F. Goodrich Company|Water absorbent polymers comprising unsaturated carboxylic acid, acrylic ester containing alkyl group 10-30 carbon atoms, and another acrylic ester containing alkyl group 2-8 carbon atoms|

---

US4978460A|1985-05-03|1990-12-18|Bluecher Hubert|Aqueous swollen macromolecule-containing system as water for firefighting|

---

US5190110A|1985-05-03|1993-03-02|Bluecher Hubert|Use of an aqueous swollen macromolecule-containing system as water for fire fighting|

---

DE3843780A1|1988-12-24|1990-07-05|Basf Ag|METHOD FOR PRODUCING FINE-PARTICLE, GEL-SHAPED, WATER-SWELLABLE COPOLYMERS|

---

US5096087A|1989-08-02|1992-03-17|Coretank, Inc.|Double containment and leak detection apparatus|

---

US5085787A|1989-11-29|1992-02-04|Air Products And Chemicals, Inc.|Crosslinked vinylamine polymer in enhanced oil recovery|

---

US5300565A|1990-04-02|1994-04-05|The Procter & Gamble Company|Particulate, absorbent, polymeric compositions containing interparticle crosslinked aggregates|

---

US5140076A|1990-04-02|1992-08-18|Nippon Shokubai Kagaku Kogyo Co., Ltd.|Method of treating the surface of an absorbent resin|

---

US5160025A|1991-08-09|1992-11-03|Uarco Incorporated|Battery shipping container|

---

US5431887A|1992-05-19|1995-07-11|Prototech Company|Flame arresting and contaminant-adsorbing filter apparatus and method in the catalytic abatement of broiler emissions|

---

US5249598A|1992-08-03|1993-10-05|Vernay Laboratories, Inc.|Bi-directional vent and overpressure relief valve|

---

US5338349A|1992-08-27|1994-08-16|Firecomp, Inc.|Fire resistant and high temperature insulating composition|

---

US5599335A|1994-03-29|1997-02-04|The Procter & Gamble Company|Absorbent members for body fluids having good wet integrity and relatively high concentrations of hydrogel-forming absorbent polymer|

---

US5647226A|1994-12-07|1997-07-15|Mainstream Engineering Corporation|Phase change apparatus for animal parts, human body parts, body fluids and culture|

---

US5559335A|1994-12-28|1996-09-24|The University Of Utah|Rotating and warping projector/backprojector for converging-beam geometries|

---

US5849210A|1995-09-11|1998-12-15|Pascente; Joseph E.|Method of preventing combustion by applying an aqueous superabsorbent polymer composition|

---

JPH10310702A|1997-05-09|1998-11-24|Kinugawa Rubber Ind Co Ltd|Hydrophilic polymer composition and production|

---

JPH1129762A|1997-07-08|1999-02-02|Osaka Ship Building Co Ltd|Water stopping composition for grout hole and water stopping|

---

US6072101A|1997-11-19|2000-06-06|Amcol International Corporation|Multicomponent superabsorbent gel particles|

---

US6222091B1|1997-11-19|2001-04-24|Basf Aktiengesellschaft|Multicomponent superabsorbent gel particles|

---

JP3554228B2|1998-07-29|2004-08-18|キヤノン株式会社|Microlens mold or mold master, and method for producing them|

---

JP2002537446A|1999-02-24|2002-11-05|ザダウケミカルカンパニー|Production of superabsorbents in emulsions with high content of internal phase|

---

WO2000055245A1|1999-03-12|2000-09-21|Basf Aktiengesellschaft|Color-stable superabsorbent polymer composition|

---

DE10013217A1|2000-03-17|2001-09-20|Basf Ag|Hydrophilic, swellable, hydrogel-forming polymers containing aluminosilicate to improve liquid permeability and odor binding properties, useful as absorbents, especially in hygienic articles|

---

AU2003270605A1|2002-09-12|2004-04-30|Bj Services Company|Compositions for thermal insulation and methods of using the same|

---

TWI241880B|2003-05-28|2005-10-11|Asustek Comp Inc|Heat sink|

---

US7670513B2|2003-07-23|2010-03-02|Basf Aktiengesellschaft|Fire control composition and method|

---

US7163969B2|2003-10-14|2007-01-16|Stockhausen, Inc.|Superabsorbent polymer aqueous paste and coating|

---

US7225882B2|2004-01-14|2007-06-05|Miller John C|Method and apparatus for retarding fire|

---

US20070001156A1|2004-08-04|2007-01-04|Toreki William Iii|Degradable or reversible fire-blocking gel|

---

TW200613623A|2004-10-21|2006-05-01|Guo-Yang Wei|Method and device for producing heat-insulative, flame-retardant and heat-isolating building component|

---

US20070054559A1|2005-09-02|2007-03-08|Maxwell Technologies, Inc.|Thermal interconnects for coupling energy storage devices|

---

US20070186577A1|2006-02-16|2007-08-16|Michael Goncharko|Passively temperature-regulated shipping container suitable for biological, pharmaceutical materials or food products|

---

US20070277707A1|2006-05-31|2007-12-06|Robbins Edward S|Double stacked pallet system for rolled sheet goods|

---

JP5196633B2|2007-08-24|2013-05-15|札幌市|Seismic isolation joint|

---

US20090069496A1|2007-09-06|2009-03-12|Sortwell Edwin T|Coherent gel coating for preventing and/or extinguishing fires|

---

KR101491138B1|2007-12-12|2015-02-09|엘지이노텍 주식회사|Multi-layer board and light emitting diode module having thereof|

---

US7992647B2|2008-09-11|2011-08-09|GelTech Solutions, Inc.|Process and device for fire prevention and extinguishing|

---

JP2010163207A|2008-12-03|2010-07-29|Masazumi Tanaka|Sample transport vessel and sample transport method|

---

US8795834B2|2009-02-09|2014-08-05|Sapturf, Llc|Synthetic turf having cooling layer|

---

DE102010035959A1|2010-08-31|2012-03-01|Li-Tec Battery Gmbh|Transport device for electrochemical energy storage devices|

---

DE102011009696A1|2011-01-28|2012-08-02|Li-Tec Battery Gmbh|Transport device for electrochemical energy storage devices|

---

AT511420A1|2011-04-21|2012-11-15|Ros Nico|PACKAGING WITH ENCLOSING HEAT BARRIER|

---

US9406917B2|2011-07-07|2016-08-02|Federal Express Corporation|Battery cooling method and system|

---

DE102012019676B4|2012-10-05|2017-10-26|Stöbich Technology Gmbh|Battery transport container, battery transport container and battery transport device|

---

US8733465B1|2013-05-22|2014-05-27|Lithfire-X, Llc|Fire suppression system for lithium ion batteries|

---

BR112017003400B1|2014-08-26|2022-01-11|Nochar, Inc|SHIPPING CONTAINER THAT HAS A FLAME RETARDANT LAYER AND A THERMAL BLOCKING LAYER|

---

KR101752384B1|2014-11-27|2017-06-30|주식회사 엘지화학|Preparation method of super absorbent polymer and super absorbent polymer prepared therefrom|

---

EP3147598A1|2015-09-28|2017-03-29|Swissmedpack Technologien JP. Buettiker GmbH|Thermo protection storage cell of a cold transport box|

---

DE102018105530A1|2018-03-09|2019-09-26|Stöbich Technology Gmbh|Battery transport device for a rechargeable battery|

---

US20210024275A1|2019-06-07|2021-01-28|James M. Kennedy|Shipping container to mitigate external fire risks|

---

US20200403192A1|2019-06-24|2020-12-24|Cheng Uei Precision Industry Co., Ltd.|Flame-retardant unit|BR112017003400B1|2014-08-26|2022-01-11|Nochar, Inc|SHIPPING CONTAINER THAT HAS A FLAME RETARDANT LAYER AND A THERMAL BLOCKING LAYER|

---

DE102016103836A1|2016-03-03|2017-09-07|Johnson Controls Advanced Power Solutions Gmbh|Battery connections for a lithium-ion battery module|

---

US10577797B2|2016-09-26|2020-03-03|Cellblock Fcs, Llc|Fire containment panel|

---

US9974987B1|2016-12-18|2018-05-22|Ron Swift|Extinguishing container kit for a flammable substance|

---

CA3076875A1|2017-09-25|2019-03-28|Call2Recycle, Inc.|Thermally protected shipping container|

---

WO2019067738A1|2017-09-27|2019-04-04|Material Technologies, Llc|Material storage and transport system|

---

DE102018105530A1|2018-03-09|2019-09-26|Stöbich Technology Gmbh|Battery transport device for a rechargeable battery|

---

US11248985B2|2019-02-15|2022-02-15|Eugene SCHREIBER|Production method and production system that detect the integrity of the hermetic seal of a container containing a product|

---

CN110649194A|2019-09-05|2020-01-03|国网湖南省电力有限公司|Energy storage battery container, battery energy storage fire-fighting system and application method thereof|

---

CN111183987A|2020-01-04|2020-05-22|辽宁中科德鑫机器人科技有限公司|Smell-luring slow-release granule and preparation method thereof|

---

CN111232383B|2020-01-20|2021-12-17|中国人民解放军陆军军医大学第二附属医院|Heat-insulation blood supply box|

法律状态:
2020-02-18| B06U| Preliminary requirement: requests with searches performed by other patent offices: procedure suspended [chapter 6.21 patent gazette]|

---

2021-10-26| B09A| Decision: intention to grant [chapter 9.1 patent gazette]|

---

2022-01-11| B16A| Patent or certificate of addition of invention granted [chapter 16.1 patent gazette]|Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 26/08/2015, OBSERVADAS AS CONDICOES LEGAIS. |

优先权:

---

申请号 | 申请日 | 专利标题

---

US201462042236P| true| 2014-08-26|2014-08-26|

---

US62/042,236|2014-08-26|

---

US14/836,591|2015-08-26|

---

PCT/US2015/047009|WO2016033223A1|2014-08-26|2015-08-26|Shipping container having a flame retardant layer and a thermal blocking layer|

---

US14/836,591|US9631773B2|2014-08-26|2015-08-26|Shipping container having a flame retardant layer and a thermal blocking layer|

---