Abstract: The present invention relates to a catalyst-supporting organic-inorganic hybrid composite particle, and more particularly, to a technique of adjusting a desired pot life and curing speed by preparing a catalyst-supporting organic-inorganic hybrid composite particle by adding a catalyst for polyurethane reaction to a catalyst-supporting particle prepared by stirring an alkoxy silane-functionalized polyurethane precursor and the tetraethyl orthosilicate for a certain period of time and mixing them, and adjusting an initiation rate for polyurethane polymerization through the prepared catalyst-supporting organic-inorganic hybrid composite particle.

Abstract: A method of manufacturing a press polymer-bonded explosive, in which a polymer emulsion is used to maximize the efficiency of a process, and a press polymer-bonded explosive manufactured using the same. The method includes a polymer-emulsion-manufacturing step of mixing a monomer of a polymer binder and an emulsifier with a process water and then adding an initiator to thus manufacture a polymer emulsion using a polymerization reaction, a slurry-manufacturing step of mixing a raw material including an explosive and an emulsion breaker with fresh process water to thus manufacture a slurry, an agglomerated-particle-forming step of adding the manufactured polymer emulsion to the manufactured slurry to thus form agglomerated particles in which a surface of the raw material is coated with the polymer binder, and an agglomerated-particle-obtaining step of collecting the agglomerated particles using filtration and drying the collected agglomerated particles.

Abstract: A synthesis of an energetic prepolymer used as a high-energy binder for an insensitive and high performance explosive is disclosed. More specifically, provided are a novel compound 2-nitratoethyl oxirane expressed by formula III, a novel compound poly(2-nitratoethyl oxirane) expressed by formula IV, obtained by polymerization of 2-nitratoethyl oxirane used as a monomer and a preparation method thereof. The compound, used as an energetic prepolymer and a monomer for preparation thereof can substitute for existing poly(glycidyl nitrate) (PGN) which has been known to be a promising one having the best performance among existing energetic prepolymers, but which has a problem to be self-decomposed after synthesis of polyurethane elastomer, to solve this problem.

Abstract: A synthesis of an energetic prepolymer used as a high-energy binder for an insensitive and high performance explosive is disclosed. More specifically, provided are a novel compound 2-nitratoethyl oxirane expressed by formula III, a novel compound poly(2-nitratoethyl oxirane) expressed by formula IV, obtained by polymerization of 2-nitratoethyl oxirane used as a monomer and a preparation method thereof. The compound, used as an energetic prepolymer and a monomer for preparation thereof can substitute for existing poly(glycidyl nitrate) (PGN) which has been known to be a promising one having the best performance among existing energetic prepolymers, but which has a problem to be self-decomposed after synthesis of polyurethane elastomer, to solve this problem.

Abstract: Disclosed are novel compounds that can be used as an energetic binder used for improving the performance and the properties of a high explosive, and a preparation method thereof. More specifically, provided are glycidyl dinitropropyl formal of chemical formula IV having a nitro group (—NO2) as an energy group and having no hydrogen bonding to carbon to which the nitro group is binding, poly(glycidyl dinitropropyl formal) of chemical formula V polymerized using the glycidyl dinitropropyl formal as a monomer, and a preparation method thereof.

Abstract: A synthesis of an energetic prepolymer used as a high-energy binder for an insensitive and high performance explosive is disclosed. More specifically, provided are a novel compound 2-nitratoethyl oxirane expressed by formula III, a novel compound poly(2-nitratoethyl oxirane) expressed by formula IV, obtained by polymerization of 2-nitratoethyl oxirane used as a monomer and a preparation method thereof. The compound, used as an energetic prepolymer and a monomer for preparation thereof can substitute for existing poly(glycidyl nitrate) (PGN) which has been known to be a promising one having the best performance among existing energetic prepolymers, but which has a problem to be self-decomposed after synthesis of polyurethane elastomer, to solve this problem.

Abstract: A synthesis of an energetic prepolymer used as a high-energy binder for an insensitive and high performance explosive is disclosed. More specifically, provided are a novel compound 2-nitratoethyl oxirane expressed by formula III, a novel compound poly(2-nitratoethyl oxirane) expressed by formula IV, obtained by polymerization of 2-nitratoethyl oxirane used as a monomer and a preparation method thereof.

Abstract: Disclosed are novel compounds that can be used as an energetic binder used for improving the performance and the properties of a high explosive, and a preparation method thereof.

Abstract: Disclosed are glycidyl di-nitropropyl carbonate and poly(glycidyl di-nitropropyl carbonate) which is prepolymer used as an energetic binder for an insensitive and high performance explosive. The present invention introduces the nitro group instead of the nitrate group, thereby enabling to provide the prepolymer having the high thermal stability (thermal decomposition initiating temperature of at least 200° C. or higher) more excellent than that of the conventional energy binder.

Abstract: Disclosed are glycidyl di-nitropropyl carbonate and poly(glycidyl di-nitropropyl carbonate) which is prepolymer used as an energetic binder for an insensitive and high performance explosive. The present invention introduces the nitro group instead of the nitrate group, thereby enabling to provide the prepolymer having the high thermal stability (thermal decomposition initiating temperature of at least 200° C. or higher) more excellent than that of the conventional energy binder.

Abstract: An energetic plascitizer comprising bis(2,2-dinitropropyl) formal, 2,2-dinitropropyl 2,2-dinitrobutyl formal and bis 2,2-dinitrobutyl) formal in a molar ratio of 20˜68%/28˜50%/4˜30% is, described. It is also provided a method for synthesizing the plasticizer comprising: dissolving 2,2-dinitropropanol and 2,2-dinitrobutanol into an organic solvent to form an organic solution, in which the molar ratio of 2,2-dinitropropanol to 2,2-dinitrobutanol is 3:1-6:1; adding to the organic solution a sulfuric acid solution where formaldehyde source was dissolved, wherein the temperature of reaction medium is maintained below 20° C.; and separating and purifying the product from the reaction mixture. The plascitizer according to the present invention has an excellent thermal and chemical properties while incurring a low production cost.

Abstract: The present invention provides an energetic plasticizer comprising bis(2,2-dinitropropyl) formal and a material that keeps bis(2,2-dinitropropyl) formal from crystallizing out, wherein the material that keeps bis(2,2-dinitropropyl) formal from crystallizing out is bis(2,2-dinitropropyl) diformal. In case where BDNPDF is used to prevent BDNPF from crystallizing out, BDNPF is not crystallized even though it stands at the temperature −20° C. for more than 6 months, while its thermal and chemical properties are similar to that of conventional plasticizers. Also, by using BDNPDF, that has been considered as a unfavorable side product, as an inhibitor of crystallization, no additional process is required to remove BDNPDF. Moreover, the cost involved is lower.

Abstract: An energetic plascitizer comprising bis(2,2-dinitropropyl) formal, 2,2-dinitropropyl 2,2-dinitrobutyl formal and bis 2,2-dinitrobutyl) formal in a molar ratio of 20˜68%/28˜50%/4˜30% is, described. It is also provided a method for synthesizing the plasticizer comprising: dissolving 2,2-dinitropropanol and 2,2-dinitrobutanol into an organic solvent to form an organic solution, in which the molar ratio of 2,2-dinitropropanol to 2,2-dinitrobutanol is 3:1-6:1; adding to the organic solution a sulfuric acid solution where formaldehyde source was dissolved, wherein the temperature of reaction medium is maintained below 20° C.; and separating and purifying the product from the reaction mixture.

Abstract: The present invention provides an energetic plasticizer comprising bis(2,2-dinitropropyl) formal and a material that keeps bis(2,2-dinitropropyl) formal from crystallizing out, wherein the material that keeps bis(2,2-dinitropropyl) formal from crystallizing out is bis(2,2-dinitropropyl) diformal. In case where BDNPDF is used to prevent BDNPF from crystallizing out, BDNPF is not crystallized even though it stands at the temperature −20° C. for more than 6 months, while its thermal and chemical properties are similar to that of conventional plasticizers. Also, by using BDNPDF, that has been considered as a unfavorable side product, as an inhibitor of crystallization, no additional process is required to remove BDNPDF. Moreover, the cost involved is lower.