The present disclosure relates to a chemiluminescent device that is suitable for propelling and that has time delay activation. The chemiluminescent device can be used in military and non-military training, and in tactical operations.
Chemiluminescent device can be used by both military and non-military organizations in training, tactical operations, and on the battlefield. These chemiluminescent devices can emit light in the visible, infrared, and ultra-violet spectrum as the result of a chemical reaction. An example of such a reaction is the activation of a fluorescer with hydrogen peroxide in the presence of a catalyst.
Traditional chemiluminescent devices are typically in the form of a tube and comprise a flexible external shell. These devices typically contain two liquid components separated from each other by a fragile barrier, such as a glass ampoule in the form of an inner tube. When light is desired from these traditional chemiluminescent devices, the separated chemical components in the device are mixed by bending the flexible tube until the glass ampoule inside the tube breaks, and then shaking the tube to mix the liquid components.
Additional chemiluminescent devibes have been proposed in which the chemiluminescence is generated by impact. These devices also contain two liquid components separated from each other by a barrier, and the components are mixed when the device impacts a target.
In certain instances, however, it may be desired to propel an unactivated chemiluminescent device to a target area, and have the device generate light after a period of time. There is therefore a need for a chemiluminescent device that can time delay the mixing of the components in the device.
It is accordingly an object in certain embodiments of the disclosure to provide a chemiluminescent device comprising a time-delay mechanism that can be triggered by the user. In certain embodiments, the time-delay mechanism can be activated by one hand of the user of the device.
One aspect of the disclosure is directed to a throwable chemiluminescent device comprising a time-delay mechanism.
Another aspect of the disclosure is directed to a throwable chemiluminescent device comprising a time-delay mechanism, wherein an oxalate component and a peroxide component are contained within the device.
Yet another aspect of the disclosure is directed to a spherically-shaped chemiluminescent device comprising a time-delay mechanism, wherein an oxalate component and a peroxide component are contained within the device.
A further embodiment of the present disclosure is directed to a throwable chemiluminescent device comprising a time-delay mechanism comprising at least two ampoules and an enclosure for the time-delay mechanism,
wherein the time-delay mechanism further comprises:
(a) a piston and a first spring, the first spring being oriented to allow movement of the piston;
(b) at least one lever, the piston being oriented to allow movement of the at least one lever; and
(c) a second spring, the second spring being oriented for movement in conjunction with the movement of the at least one lever,
wherein an oxalate component is contained in one of the at least two ampoules, and a peroxide component is contained in another of the at least two ampoules, and
wherein the time-delay mechanism delays the chemiluminescent reaction of the oxalate component and the peroxide component.
Additional objects and advantages of the disclosure will be set forth in part in the description which follows, and in part will be obvious from the description, or may be learned by practice of the disclosure. The objects and advantages of the present disclosure will be realized and attained by means of the elements and combinations particularly pointed out in the appended claims.
It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory only and are not restrictive of the disclosure, as claimed.
The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate several embodiments of the disclosure and together with the description, serve to explain the principles of the disclosure.
The time-delay mechanism 14 and ampoules 16 and 18 according to the present disclosure can be contained in an enclosure of any shape that is capable of being propelled, either by a machine or by a human. In the embodiment depicted in
The enclosure can be formed of any material that is capable of being shaped, and that also will not adversely affect the reaction between the chemiluminescent components that react within the device. Suitable materials include thermoplastic resins such as polypropylene, low density polyethylene, high density polyethylene, and polyolefin copolymers. In certain embodiments, the two sides of the enclosure are sealed without a flange. The enclosure can be opaque, transparent and/or partially transparent. In some embodiments, the enclosure is colored in order to block visible light, but still allow infra-red light and/or ultra-violet to be detected. in certain embodiments, the enclosure is purple in color. The time delay mechanism according to the present disclosure can be contained in any of the enclosures contemplated above.
The external sphere depicted in
In
The materials that can be used make the components of the time-delay mechanism according to the present disclosure can be any material that does not adversely affect the reaction between the chemiluminescent components that react within the device according to the present disclosure. In certain embodiments, some of the components of the time-delay mechanism, such as the components that form the pivot points, can be made from stainless steel.
In certain embodiments, the time-delay mechanism according to the present disclosure delays time for a period ranging up to 120 seconds from the time the time-delay mechanism has been activated. For example, the time delay can range from 1 to 60 seconds, such as from 1 to 30 seconds, from 2 to 20 seconds, from 3 to 15 seconds, from 4 to 10 seconds, from 4 to 8 seconds, from 4 to 6 seconds, from 3 to 10 seconds, from 3 to 8 seconds, and from 3 to 5 seconds.
The total weight of the chemiluminescent devices can vary greatly depending on the intended application for the device. For purposes of the present disclosure, the total weight of the chemiluminescent device includes the weight of the enclosure, the weight of the time-delay mechanism, and the weight of the chemiluminescent components that react within the device. In certain embodiments, the chemiluminescent device according to the present disclosure can have a weight ranging from 50 grams to 500 grams. In these embodiments, suitable weight ranges include, for example, from 75 grams to 450 grams, from 100 grams to 400 grams, from 110 grams to 350 grams, from 120 grams to 300 grams, from 130 grams to 250 grams, from 130 grams to 200 grams, from 135 grams to 175 grams, from 135 grams to 160 grams, and from 150 to 165 grams, from 155 to 165 grams, and from 140 grams to 150 grams. In one embodiment of the present disclosure, the chemiluminescent device has a total weight ranging from 140 grams to 150 grams. In another embodiment of the present disclosure, the chemiluminescent device has a total weight ranging from 155 grams to 165 grams.
In certain embodiments, the chemiluminescent device is throwable. In these embodiments, the shape of the device can be any shape that is able to be thrown by the user. Non-limiting examples of the shape of the device include shapes chosen from spherical shapes, oblong shapes, cylindrical shapes, wedge shapes, disc shapes, and football shapes. In these embodiments, the size of the device is limited only by the ability of the user to throw the device.
In certain embodiments, the device is spherically shaped and has a diameter ranging from 40 mm to 225 mm. In these embodiments, suitable diameter ranges include, for example, from 50 mm to 200 mm, from 50 mm to 150 mm, from 50 mm to 100 mm, from 60 mm to 120 mm, from 60 mm to 100 mm, from 60 mm to 80 mm, from 70 mm to 100 mm, from 70 mm to 90 mm, from 70 mm to 80 mm, from 70 mm to 75 mm, and from 72 mm to 77 mm. In one embodiment of the present disclosure, the chemiluminescent device is spherically shaped, has a total weight ranging from 140 grams to 150 grams, and has a diameter ranging from 72 mm to 77 mm. In another embodiment of the present disclosure, the chemiluminescent device is spherically shaped, has a total weight ranging from 155 grams to 165 grams, and has a diameter ranging from 70 mm to 75 mm.
The chemiluminescent device according to the present disclosure comprises at least two chemiluminescent components, which are maintained separately until activation. The first component is comprised of at least one oxalate ester, and the second component is comprised of at least one peroxide.
In certain embodiments, the first component comprising at least one oxalate ester is contained in one ampoule, and the second component comprising at least one peroxide is contained in another ampoule. In additional embodiments, the first component comprising at least one oxalate ester is contained within the ampoules present in the chemiluminescent device according to the present disclosure, and the second component comprising at least one peroxide is separately contained within the enclosure shell of the device. In yet another embodiment of the present disclosure, the second component comprising at least one peroxide is contained within the ampoules present in the chemiluminescent device according to the present disclosure, and the first component comprising at least one oxalate ester is separately contained within the enclosure shell of the device.
With respect to the first component, examples of the at least one oxalate useful in the present disclosure include bis(2,4,5-trichloro-6-carbopentoxyphenyl)oxalate; bis(2,4,5-trichlorophenyl)oxalate; bis(2,4,5-tribromo-6-carbohexoxyphenyl)oxalate; bis(2,4,5-trichloro-6-carboisopentoxyphenyl)oxalate; bis(2,4,5-trichloro-6-carbobenzoxyphenyl)oxalate; bis(2-nitrophenyl)oxalate; bis(2,4-dinitrophenyl)oxalate; bis(2,6-dichloro-4-nitrophenyl)oxalate; bis(2,4,6-trichlorophenyl)oxalate; bis(3-trifluoromethyl-4-nitrophenyl)oxalate; bis(2-methyl-4,6-dinitrophenyl)oxalate; bis(1,2-dimethyl-4,6-dinitrophenyl)oxalate; bis(2,4-dichlorophenyl)oxalate; bis(2,4-dinitrophenyl)oxalate; bis(2,5-dinitrophenyl)oxalate; bis(2-formyl-4-nitrophenyl)oxalate; bis(pentachlorophenyl)oxalate; bis(1,2-dihydro-2-oxo-1-pyridyl)glyoxal; bis(2,4-dinitro-6-methylphenyl)oxalate; bis-N-phthalimidyl oxalate, oxalates represented by the general formula (I)
wherein R═CH2A and A is chosen from alkyl chains, alkyl rings, and aromatic rings or combinations thereof, such that R is nonlinear and such that R comprises from 4-15 carbons, and mixtures of any of the foregoing oxalates.
Examples of oxalates represented by formula (I) include:
Additional examples of oxalates represented by general formula (I) are disclosed in U.S. Published Application No. 2011-0084243, the disclosure of such oxalates being incorporated herein by reference.
In certain embodiments, the first component can further comprise at least one fluorescer. Examples of the at least one fluorescer useful in the present disclosure include 1-methoxy-9,10-bis(phenylethynyl)anthracene, perylene, rubrene, 16,17-didecycloxyviolanthrone, 2-ethyl-9,10-bis(phenylethynyl)anthracene; 2-chloro-9,10-bis(4-ethoxyphenyl)anthracene; 2-chloro-9,10-bis(4-methoxyphenyl)anthracene; 9,10-bis(phenylethynyl)anthracene; 1-chloro-9,10-bis(phenylethynyl)anthracene; 1,8-dichloro-9,10-bis(phenylethynyl)anthracene; 1,5-dichloro-9,10-bis(phenylethynyl)anthracene; 2,3-dichloro-9,10-bis(phenylethynyl)anthracene; 5,12-bis(phenylethynyl)tetracene; 9,10-diphenylanthracene; 1,6,7,12-tetraphenoxy-N,N′-bis(2,6-diisopropylphenyl)-3,4,9,10-perylene dicarboximide; 1,6,7,12-tetraphenoxy-N,N′-bis(2,5-di-t-butylphenyl)-3,4,9,10-perylene dicarboximide; 1,7-di-chloro-6,12-diphenoxy-N,N′-bis(2,6-diisopropylphenyl)-3,4,9,10-perylene dicarboximide; 1,6,7,12-tetra(p-bromophenoxy)-N,N′-bis(2,6-diisopropylphenyl)-3,4,9,10-perylene dicarboximide; 1,6,7,12-tetraphenoxy-N,N′-di-neopentyl-3,4,9,10-perylene dicarboximide; 1,6,7,12-tetra(p-t-butylphenoxy)N,N′-dineopentyl-3,4,9,10-perylene dicarboximide; 1,6,7,12-tetra(o-chlorophenoxy)-N,N′-bis(2,6-diisopropylphenyl)-3,4,9,10-perylene dicarboximide; 1,6,7,12-tetra(p-chlorophenoxy)-N,N′-bis(2,6-diisopropylphenyl)-3,4,9,10-perylene dicarboximide; 1,6,7,12-tetra(o-fluorophenoxy)-N,N′-bis(2,6-diisopropylphenyl)-3,4,9,10-perylene dicarboximide; 1,6,7,12-tetra(p-fluorophenoxy)-N,N′ bis(2,6-diisopropylphenyl)-3,4,9,10-perylene dicarboximide; 1,6,7,12-tetraphenoxy-N,N′-diethyl-3,4,9,10-perylene dicarboximide; 1,7-dibromo-6,12-diphenoxy-N,N′-bis(2-isopropylphenyl)-3,4,9,10-perylene dicarboximide; 16,17-dihexyloxyviolanthrone; rubrene; 1,4-dimethyl-9,10-bis(phenylethynyl)anthracene, and mixtures thereof.
The amount of the at least one oxalate and the at least one fluorescer employed is upwardly limited only by the solubility of the ester and fluorescer in the solvent chosen. However, as would be appreciated by one in the art, the efficiency of the reaction would decrease at certain high concentrations.
In certain embodiments, the at least one oxalate is present in an amount ranging from 3 percent to 60 percent by weight, based on the total weight of the two-part composition. For example, the at least one oxalate can be present in an amount ranging from 3 percent to 50 percent by weight, based on the total weight of the two-part composition, such as from 3 percent to 40 percent by weight, from 3 percent to 30 percent by weight, from 5 percent to 25 percent by weight, and from 7 percent to 25 percent by weight. In certain embodiments, the at least one fluorescer is present in an amount ranging from 0.05 percent to 0.9 percent by weight based on the total weight of the two-part composition. For example, the at least one fluorescer can be present in an amount ranging from greater than 0.05 percent by weight to 0.9 percent by weight, based on the total weight of the two-part composition, such as from greater than 0.1 percent by weight, from greater than 0.2 percent by weight, from greater than 0.3 percent by weight, from greater than 0.4 percent by weight, from greater than 0.5 percent by weight, from greater than 0.6 percent by weight, from greater than 0.7 percent by weight, and from greater than 0.8 percent by weight. In addition, the at least one fluorescer can be present in an amount ranging from 0.05 percent by weight to less than 0.9 percent by weight, based on the total weight of the two-part composition, such as from less than 0.8 percent by weight, from less than 0.7 percent by weight, from less than 0.6 percent by weight, from less than 0.5 percent by weight, from less than 0.4 percent by weight, from less than 0.3 percent by weight, from less than 0.2 percent by weight, and from less than 0.1 percent by weight. It is also intended that the amount of the at least one oxalate and the at least one fluorescer can range between any of the numerical values listed above.
With respect to the second component, examples of the at least one peroxide useful in the present disclosure include hydrogen peroxide; sodium peroxide; sodium perborate; sodium pyrophosphate peroxide; urea peroxide; histidine peroxide; t-butyl-hydroperoxide; and peroxybenzoic acid, and mixtures thereof. In certain embodiments, the at least one peroxide is present in an amount ranging from 0.25 percent to 25 percent by weight, based on the total weight of the two-part composition. For example, the at least one peroxide can be present in an amount ranging from 0.25 percent to 20 percent by weight, based on the total weight of the two-part composition, such as from 0.5 percent to 20 percent by weight, from 0.5 percent to 15 percent by weight, from 0.5 percent to 10 percent by weight, and from 0.5 percent to 6 percent by weight. In certain embodiments, the at least one peroxide of the present disclosure can be hydrogen peroxide.
In certain embodiments, the second component can further comprise at least one catalyst. Examples of the at least one catalyst useful in the present disclosure include sodium salicylate, lithium salicylate, 5-chlorolithium salicylate, triazoles (e.g., 1,2,3-triazole and 1,2,4-triazole), substituted triazoles (e.g., substituted 1,2,3-triazole and substituted 1,2,4-triazole), imidazoles, and substituted imidazoles.
In certain embodiments, the at least one catalyst is present in an amount ranging from 0.0005 percent to 0.5 percent by weight, based on the total weight of the two-part composition. For example, the at least one catalyst can be present in an amount ranging from greater than 0.0005 percent by weight to 10 percent by weight, based on the total weight of the two-part composition, such as from 0.001 percent or greater by weight, from 0.005 percent or greater by weight, from 0.01 percent or greater by weight, from 0.05 percent or greater by weight, from 0.1 percent or greater by weight, from 0.25 percent or greater by weight, from 0.5 percent or greater by weight, from 1 percent or greater by weight, from 1.5 percent or greater by weight, from 2 percent or greater by weight, from 2.5 percent or greater by weight, from 3 percent or greater by weight, from 3.5 percent or greater by weight, from 4 percent or greater by weight, from 4.5 percent or greater by weight, from 5 percent or greater by weight, and from 7.5 percent or greater by weight. In addition, the at least one catalyst can be present in an amount ranging from 0.0005 percent by weight to less than 10 percent by weight, based on the total weight of the two-part composition, such as from 7.5 percent or less by weight, from 5 percent or less by weight, from 4.5 percent or less by weight, from 4 percent or less by weight, from 3.5 percent or less by weight, from 3 percent or less by weight, from 2.5 percent or less by weight, from 2 percent or less by weight, from 1.5 percent or less by weight, from 1 percent or less by weight, from 0.5 percent or less by weight, from 0.25 percent or less by weight, from 0.1 percent or less by weight, from 0.05 percent or less by weight, from 0.01 percent or less by weight, from 0.005 percent or less by weight, and from 0.001 percent or less by weight. It is also intended that the amount of at least one catalyst can range between any of the numerical values listed above.
The chemiluminescent device according to the present disclosure can also comprise at least one carrier in the first and/or second component. Examples of the at least one carrier useful in the present disclosure include dimethyl phthalate, dibutyl phthalate, dioctal phthalate, butyl benzoate, acetyl triethyl citrate, triethyl citrate, ethylene glycol dibenzoate, and propylene glycol dialkyl ether containing one to three propylene moieties and each alkyl group is independently a straight-chain or branched-chain alkyl group containing up to 8 carbon atoms. Exemplary solvents include dimethyl phthalate, triethyl citrate, ethylene glycol dibenzoate, propylene glycol dialkyl ethers containing two propylene moieties such as dipropylene glycol dimethyl ether, dipropylene glycol diethyl ether and dipropylene glycol di-t-butyl ether, dibutyl phthalate, butyl benzoate, propylene glycol dibenzoate, ethyl-hexyl diphenyl phosphate, and mixtures thereof.
In certain embodiments, the at least one carrier is present in an amount ranging from 5 percent to 95 percent by weight, based on the total weight of the two-part composition. For example, the at least one carrier can be present in an amount ranging from greater than 5 percent by weight to 95 percent by weight, based on the total weight of the two-part composition, such as from greater than 10 percent by weight, from greater than 20 percent by weight, from greater than 30 percent by weight, from greater than 40 percent by weight, from greater than 50 percent by weight, from greater than 60 percent by weight, from greater than 70 percent by weight, from greater than 80 percent by weight, and from greater than 90 percent by weight. In addition, the at least one carrier can be present in an amount ranging from 5 percent by weight to less than 95 percent by weight, based on the total weight of the two-part composition, such as from less than 90 percent by weight, from less than 80 percent by weight, from less than 70 percent by weight, from less than 60 percent by weight, from less than 50 percent by weight, from less than 40 percent by weight, from less than 30 percent by weight, from less than 20 percent by weight, and from less than 10 percent by weight. It is also intended that the amount of at least one carrier can range between any of the numerical values listed above.
The light generated upon activation of the chemiluminescent device according to the present disclosure may be light visible in the ultra-violet, infra-red and/or visible light spectrums. In certain embodiments, visible light is generated upon activation of the chemiluminescent device and this light last for up to 5 minutes, such as, for example, up to 4 minutes, up to 3 minutes, up to 2 minutes, up to 1 minute, up to 45 seconds, up to 30 seconds, and up to 20 seconds. In certain embodiments, infra-red light is generated upon activation of the chemiluminescent device and this light last for up to 60 minutes, such as, for example, up to 50 minutes, up to 45 minutes, up to 40 minutes, up to 30 minutes, up to 20 minutes, up to 15 minutes, up to 10 minutes, and up to 5 minutes. It is contemplated that the chemiluminescent device according to the present disclosure can generate light in the ultra-violet spectrum, the infra-red spectrum, the visible light spectrum, and any combination thereof.
Additional components that may be included in either component of the chemiluminescent device include, but are not limited to, thickeners to allow the marker to stick to the target better, fluorescent powders for day time target marking, and antifreeze agents to prevent freezing, film formers, gelling agents, polyacrylamides, and polyvinylchloride. These additional components are those well known in the art to be suitable for the above purposes.
The present application claims priority to U.S. Provisional Patent Application No. 61/442,140, filed Dec. 11, 2010, which is incorporated herein by reference.
Number | Date | Country | |
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61422140 | Dec 2010 | US |