Classifications

• • C—CHEMISTRY; METALLURGY
  • C06—EXPLOSIVES; MATCHES
  • C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
  • C06B21/00—Apparatus or methods for working-up explosives, e.g. forming, cutting, drying
  • C06B21/0033—Shaping the mixture
  • C06B21/0075—Shaping the mixture by extrusion
• • C—CHEMISTRY; METALLURGY
  • C06—EXPLOSIVES; MATCHES
  • C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
  • C06B25/00—Compositions containing a nitrated organic compound
  • C06B25/10—Compositions containing a nitrated organic compound the compound being nitroglycerine
  • C06B25/12—Compositions containing a nitrated organic compound the compound being nitroglycerine with other nitrated organic compounds
• • C—CHEMISTRY; METALLURGY
  • C06—EXPLOSIVES; MATCHES
  • C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
  • C06B25/00—Compositions containing a nitrated organic compound
  • C06B25/18—Compositions containing a nitrated organic compound the compound being nitrocellulose present as 10% or more by weight of the total composition
• • C—CHEMISTRY; METALLURGY
  • C06—EXPLOSIVES; MATCHES
  • C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
  • C06B31/00—Compositions containing an inorganic nitrogen-oxygen salt
  • C06B31/02—Compositions containing an inorganic nitrogen-oxygen salt the salt being an alkali metal or an alkaline earth metal nitrate
  • C06B31/04—Compositions containing an inorganic nitrogen-oxygen salt the salt being an alkali metal or an alkaline earth metal nitrate with carbon or sulfur

Definitions

• the present invention relates to improved explosive compositions and to a method of manufacturing-said compositions. More particularly, the present invention concerns explosive compositions which exhibit a high detonating activity and reaction velocity and therefore are useful, for example, in propellant charges, primer charges, igniting charges, and the like.
• Black powder which is basically a mixture of saltpeter (potassium nitrate), carbon and sulfur, is characterized by good ignitability, a constant igniting capacity and a uniform burning consumption. It is well known in the prior art that nitrocellulose can be mixed with black powder to produce an explosive composition which is capable of generating a greater amount of gas and heat than that generated by black powder alone, While maintaining all of the other aforementioned advantages characteristics of black powder.
• this mixture of nitrocellulose and black powder has many disadvantages, which include, for example, the undesirable influence of the sulfur contained in the black powder on the stability of nitrocellulose at higher temperatures, say over 100 C., the formation of toxic sulfur reaction products, particularly hydrogen sulfide, during the burning of the black powder in the presence of nitrocellulose, which may involve considerable danger depending upon its place of use, and further the causing of heavy fouling on breech mechanisms and other firing components when black powder is fired as a mixture with nitrocellulose.
• An object of the present invention is to produce an improved explosive composition which exhibits a high detonating activity and reaction velocity and therefore is useful in propellant charges, primer or detonating charges, igniting charges, and the like.
• a further object of the present invention is to produce an explosive composition which has all of the advantages of black powder and mixtures of black powder with nitrocellulose while substantially eliminating the disadvantages.
• a still further object of the present invention is to provide an improved method for manufacturing the explosive composition of the present invention.
• Another object of the present invention is to produce an explosive composition which exhibits improved stability at high temperatures, the substantial elimination of the formation of toxic sulfur reaction products while the explosive is being consumed, and an overall improvement in the operation of firing and breech mechanisms.
• the explosive composition of the present invention exhibits only a minor mechanical strength since the granules formed of saltpeter and charcoal therein, constituting a sulfur-free powder with specific properties, are adhered to each other only slightly by the nitrocellulose.
• the explosive compositions or detonating charge of the present invention exhibits a substantially higher detonating activity as Well as a higher reaction velocity.
• the advantage of using charcoal as compared to other carbon carriers, for example carbon black, is based on the high content of volatile components in the charcoal which exert an accelerating effect upon the reaction of the mixture.
• One of the features of the present invention resides in the fact that the nitrates (oxidizer) which are employed are first mixed and combined separately with the charcoal as a carbonaceous binder, and are manufactured in the form of a finely particulate, accurately dimensioned product, and are thereafter kneaded together with the alcohol-moist nitrocellulose to form a plastic mass.
• the specific properties of the gun powder are particularly apparent, in addition to the specific properties of nitrocellulose, that is a hot flame and a high amount of gas.
• the amount of nitrocellulose present with the charcoal binder-oxidizer mixture to form the explosive composition of the present invention will vary depending upon the particular use for which it is intended.
• the explosive composition of the present invention will contain about 20 to 80% by weight, preferably 30 to 50% by weight, of nitrocellulose and about 80 to 20% by weight, preferably about 70 to 50% by weight, of the charcoal binder-oxidizer mixture.
• the charcoal binder-oxidizer mixture may contain about 5 to 30% by weight of the charcoal binder and about 95 to 70% by weight of the oxidizer. More particularly, the binder is present in an amount of about to by weight and the oxidizer is an amount of about 90 to 75% by weight.
• the carbonaceous binder used in the present invention is limited to charcoal.
• the advantage of using charcoal as compared to other carbon carriers, e.g. carbon black is based on the high content of volatile components in the charcoal which exerts an accelerating effect upon the reaction of the mixture.
• the oxidizer employed in the composition of the present invention can be any of the inorganic nitrates such as, for example, ammonium nitrate, and nitrates of the alkali and alkaline earth metals, such as sodium nitrate, potassium nitrate (saltpeter), calcium nitrate, magnesium nitrate, strontium nitrate and beryllium nitrate.
• the oxidizers potassium nitrate is preferred. Effective results can also be obtained with mixtures of any one of the above nitrates, for example, a mixture of sodium nitrate with ammonium nitrate.
• the amount of oxidizer used will vary depending upon the sensitivity and explosive elfect desired, and these in turn are dependent upon the particular nitrate or nitrates used. Because of the high oxidizer content and the use of charcoal, the explosive composition of the present invention has a substantially higher detonating activity and reaction velocity than compositions using small amounts of oxidizer and carbonaceous binders other than charcoal.
• the explosive compositions of the present invention can be mixed with various adjuvants such as solvents, plasticizers, stabilizers, ballistic modifiers, and the like.
• suitable solvents include organic alcohols, such as for example, ethyl alcohol, isopropyl alcohol, tertiary-butyl alcohol, alkoxy alcohols, such as diethyline glycol, phenol, etc.; ethers, such as for example, ethyl ether, tertiarybutyl methyl ether, benzyl phenyl ether, etc.; ketones, such as for example, acetones, ethylmethyl ketone, diphenyl ketone, etc.; esters such as for example, butyl acetate and isopropyl acetate, and various other hydrocarbons including, for example, benzene and toluene.
• plasticizers which can also act as solvents and energizing modifiers are added to the explosive composition of the present invention.
• plasticizers include nitroglycerin, butane triol trinitrate, ethylene glycol dinitrate and the like. These materials may be mixed with one or more miscible deterrents, such as, butyl phthalate, dimethylsebacate, dibutyl succinate, dibutyl adipate, triacetin, ethyl diphenyl phosphate, tributyl phosphate, and the like.
• the preferred plasticizer is nitroglycerin which is advantageously present in an amount up to about 1% by weight.
• Suitable stabilizing agents include diphenylamine, 2-nitrodiphenylamine, the centralites and many others. Other ingredients, such as dioctylphathalate, lead stearate, red lead, dinitrotoluene, and the like, may be incorporated in the explosive composition of the present invention to obtain particular ballistic properties, as desired.
• the explosive mixture of the present invention is readily prepared by mixing the ingredients in a particular manner.
• the charcoal binder-oxidizer mixture is in a finely granulated form before it is kneaded together with the nitrocellulose to form a plastic mass.
• the amount of solvent which can be used in the explosive composition of the present invention will vary, depending upon, for example, the amount of plasticizer present and also upon the desired consistency of the mixture, which can vary from a gelled oil or thick, barely pourable mixture, to a quick-flowing liquid.
• the ratio of the solvent to the explosive composition for example, can range from about 1 to l to about 20 to 1, and even higher, preferably about 3 to 1 to about 15 to 1.
• the explosive composition is prepared in gelatinous sheet form.
• Gelatinization is effected by rolling the explosive mixture with heat rolls, supplemented by intermediate kneading.
• the resulting sheet can then be inserted into an extruding dye where the composition may be extruded by conventional extrusion techniques.
• a typical method for producing suitable grains from explosive compositions is an extrusion technique in which the explosive composition, in a flowable form is introduced into a hopper and the product extruded by screw extrusion into suitable grains. The extruded product can then be cut into the desired length and dried.
• Example I 2.8 kg. of nitrocellulose, moistened with ethyl alcohol, is kneaded with 2-3 liters of ethyl ether. Thereafter, 4.2 kg. of a mixture of potassium nitrate and charcoal, consisting of by weight of potassium nitrate and 20% by weight of charcoal, is added and the resultant mix is kneaded for about two hours. During the kneading procedure, 1% by weight of dibutyl phthalate (plasticizer) and 1% by weight of acardite (stabilizer) are added. The mass, kneaded into a compressible condition, is pressed through a nozzle, cut into pieces of desired length and dried.
• plasticizer dibutyl phthalate
• acardite stabilizer
• EXAMPLE II 2.1 kg. of nitrocellulose, moistened with ethyl alcohol, is kneaded with 22.5 liters of ethyl ether. Then, 4.9 kg. of a mixture of potassium nitrate and charcoal, the latter being in an extremely fine particulate form, containing about 75 by weight of potassium nitrate and 25% by weight of charcoal, as well as 1% by weight of acardite II and about 1% by weight of nitroglycerin are added and the resultant mix is kneaded for about two hours to form a compressible mass. The kneaded mass is pressed through a nozzle, cut into the desired length and dried.
• Acardite II is a urea derivative, similar to centralite, but having one less ethyl residue. The structural formula thereof is We claim:
• An explosive composition which comprises about 20 to 80% by weight nitrocellulose and about 80 to 20% by weight of a charcoal binder-inorganic nitrate oxidizer salt mixture, said mixture containing about 5 to 30% by weight of the charcoal binder and about to 70% by weight of the oxidizer.
• composition of claim 1, wherein the oxidizer is potassium nitrate.
• composition of claim 1 wherein the explosive composition also contains a solvent selected from the group consisting of alcohols, ethers, esters, ketones, and mixtures thereof.
• composition of claim 3 wherein the solvent is a mixture of ethyl alcohol and ethyl ether.
• composition of claim 1 wherein the explosive mixture contains up to about 1% by weight of a plasticizer.
• composition of claim 5 wherein the plasticizer is nitroglycerin.
• An explosive composition comprising about to by Weight nitrocellulose and about to 50% by weight of a charcoal binder inorganic nitrate oxidizer salt mixture, said mixture containing about 10 to 25% by weight of the charcoal, and about to by weight of the oxidizer and up to about 1% by weight of nitroglycerin.
• composition of claim 7, wherein the plasticizer is nitroglycerin.
• composition of claim 8 wherein the explosive composition also contains a solvent comprising a mixture of ethyl alcohol and ethyl ether.
• a process for producing an explosive composition which comprises mixing about 5 to 30% by weight, of a charcoal binder with about to 70% by weight oi an inorganic nitrate oxidizer salt to form a finely particulate, accurately dimentioned product, adding about 20 to 80% by Weight of nitrocellulose, which has been previously moistened with ethyl alcohol and kneaded with ethyl ether, to about 80 to 20% by weight of said particulate product kneading the mixture until an extrudable consistency is obtained, extruding the resulting composition, cutting the extruded product into the desired length, and drying the extruded product.

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Health & Medical Sciences (AREA)
• Emergency Medicine (AREA)
• Inorganic Chemistry (AREA)
• Compositions Of Macromolecular Compounds (AREA)
• Agricultural Chemicals And Associated Chemicals (AREA)
• Air Bags (AREA)

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Cited By (7)

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Citations (2)

• 0
  • DE DENDAT1302998D patent/DE1302998B/de active Pending
• 1965
  • 1965-08-21 DE DE19651446919 patent/DE1446919A1/de active Pending
• 1966
  • 1966-06-28 FI FI661720A patent/FI46371C/fi active
  • 1966-08-11 LU LU51752A patent/LU51752A1/xx unknown
  • 1966-08-15 CH CH1174266A patent/CH481029A/de not_active IP Right Cessation
  • 1966-08-18 IL IL26356A patent/IL26356A/xx unknown
  • 1966-08-19 NL NL6611746A patent/NL6611746A/xx unknown
  • 1966-08-19 BE BE685750D patent/BE685750A/xx unknown
  • 1966-08-19 GB GB37382/66A patent/GB1155323A/en not_active Expired
• 1968
  • 1968-03-01 US US709839A patent/US3473982A/en not_active Expired - Lifetime

Patent Citations (2)

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