Abstract:
2,2,2-trifluoroethoxy bis(2-fluoro-2,2-dinitroethoxy)methane, CF.sub.3 CHb.2 OCH[OCH.sub.2 CF(NO.sub.2).sub.2 ].sub.2, is an energetic plasticizer useful in plastic-bonded explosives. Of particular importance is its miscibility with fluoropolymers.
Abstract:
Bis(2-fluoro-2,2-dinitroethoxy)acetonitrile, N.tbd.C--CH[OCH.sub.2 CF(NO..2).sub.2 ].sub.2, is useful as a coplasticizer with bis(2-fluoro-2,2-dinitroethyl)formal in energetic plasticizer mixtures for plastic bonded explosives.
Abstract:
Bis(2-fluoro-2,2-dinitroethoxy)(1-fluoro-1,1-dinitro-2-propoxy)methane wh is useful as an energetic coplasticizer with bis(2-fluoro-2,2-dinitroethyl)formal in plastic-bonded explosives.
Abstract:
Bis(2-fluoro-2,2-dinitroethoxy) 2,2,3,3,4,4,4-heptafluorobutoxymethane, (F), CF.sub.3 CF.sub.2 CF.sub.2 CH.sub.2 OCH[OCH.sub.2 CF(NO.sub.2).sub.2 ].sub.2, is an energetic plasticizer with a melting point of -18.degree. C. and thermal stability up to 150.degree. C. HFBF is miscible with polyfluoro- and polynitropolymers and useful as a plasticizer in plastic-bonded explosives.
Abstract:
A process for producing 1,3,5-trifluoro-2,4,6-trinitrobenzene by:(1) forming a mixture of fuming sulfuric acid and potassium nitrate wherein the fuming sulfuric acid is composed of at least 25 percent by weight sulfur trioxide, and wherein the molar ratio of fuming sulfuric acid to potassium nitrate is from about 2:1 to about 3:1;(2) adding 1,3,5-trifluorobenzene to the mixture until the molar ratio of potassium nitrate to 1,3,5-trifluorobenzene is from 6:1 to 10:1, the temperature of the mixture being maintained in the range of from about 30.degree. C. to about 50.degree. C. during the addition;(3) then raising the temperature of the mixture into the range of from about 140.degree. C. to about 160.degree. C. where it is maintained until the optimum yield of 1,3,5-trifluoro-2,4,6-trinitrobenzene has been obtained; and(4) isolating the product, 1,3,5-trifluoro-2,4,6-trinitrobenzene from the reaction mixture.
Abstract:
A new compound 2,2-dinitrobutyl 2,2-dinitropropyl formal (DNBPF),CH.sub.3 C(NO.sub.2).sub.2 CH.sub.2 CH.sub.2 OCH.sub.2 OCH.sub.2 C(NO.sub.sub.2 CH.sub.3,and a energetic plasticizer which is a 1:1 eutectic mixture of DNBPF and bis(2,2-dinitropropyl) formal.
Abstract translation:新型化合物2,2-二硝基丁基2,2-二硝基丙基(DNBPF),CH 3 C(NO 2)2 CH 2 CH 2 OCH 2 OCH 2 C(NO 2)2 CH 3,以及能量增塑剂,其为DNBPF和双(2,2-二硝基丙基 )正式。
Abstract:
An energetic uncured binder composite mixture comprising(1) a hydroxy-terminated polyfluoroformal prepolymer of the general formulaHOCH.sub.2 (CF.sub.2).sub.n CH.sub.2 [OCH.sub.2 OCH.sub.2 (CF.sub.2).sub.nH.sub.2 ].sub.m OH wherein n is 3 or 4 and m is selected to provide a number average molecular weight of from about 1,000 to about 10,000 for the prepolymer; and(2) an energetic plasticizer which isbis(2,2-dinitropropyl)formal,bis(2,2-trinitroethyl)formal,bis(2-fluoro-2,2-dinitroethyl)formal,bis(2,2-difluoro-2-nitroethyl)formal,2,2-dinitropropyl 2-fluoro-2,2-dinitroethyl formal, or mixtures thereof;wherein the weight ratio of energetic plasticizer to prepolymer is from about 2:1 to about 5:1. This binder composite mixture is useful for preparing energetic plastic bonded explosives having high chemical and thermal stabilities.
Abstract translation:一种能量未固化的粘合剂复合材料混合物,其包含(1)通式为HOCH 2(CF 2)n CH 2 [OCH 2 OCH 2(CF 2)n CH 2] m OH的羟基封端的多氟代预聚物,其中n为3或4并且m被选择以提供数均分子量 对于预聚物为约1,000至约10,000; 和(2)能量增塑剂,其为双(2,2-二硝基丙基)甲醛,双(2,2-三硝基乙基)甲醛,双(2-氟-2,2-二硝基乙基)甲醛,双(2,2-二氟 -2-硝基乙基)甲醛,2,2-二硝基丙基2-氟-2,2-二硝基乙基甲醛或其混合物; 其中能量增塑剂与预聚物的重量比为约2:1至约5:1。 该粘合剂复合混合物可用于制备具有高化学和热稳定性的高能塑料粘结炸药。
Abstract:
4,4,10,10-tetranitro-6,8-dioxatridecane-1,13-diol polyformal, HO(CH.sub.2ub.3 C(NO.sub.2).sub.2 CH.sub.2 OCH.sub.2 OCH.sub.2 C(NO.sub.2).sub.2 (CH.sub.2).sub.3 O[CH.sub.2 O(CH.sub.2).sub.3 C(NO.sub.2).sub.2 CH.sub.2 OCH.sub.2 OCH.sub.2 C(NO.sub.2).sub.2 (CH.sub.2).sub.3 O].sub.n H, which has high energy, high thermal stability, and which is useful as a prepolymer for plastic-bonded explosive compositions.
Abstract:
One mole of 2,2,3,3,4,4-hexafluoropentane-1,5-diol is reacted with one molef formaldehyde in the presence of an excess of trifluoromethanesulfonic acid to produce 1,3-dioxa-5,5,6,6,7,7-hexafluorocyclooctane.