US2353147A - High-density explosive charge - Google Patents
High-density explosive charge Download PDFInfo
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- US2353147A US2353147A US396655A US39665541A US2353147A US 2353147 A US2353147 A US 2353147A US 396655 A US396655 A US 396655A US 39665541 A US39665541 A US 39665541A US 2353147 A US2353147 A US 2353147A
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- ammonium nitrate
- organic
- molten
- trinitrotoluene
- blend
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- 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
- C06B21/005—By a process involving melting at least part of the ingredients
Definitions
- This invention relates to high density explosive charges and more particularly to methods of preparing such charges in a form adapted. to fill readily into containers.
- High density is an essential characteristic "of many types of explosive charges since it permits the attainment of high, bull; strength.
- shell charges for military use for example, the highest density consistent with satisfactory initiating and propagating ability is desirable.
- Cast explosives representone efiective method of obtaining this result.
- a high density charge may be prepared by exposing a mixture of more than one compound of a predetermined blend to a temperature at which one of the compounds becomes at least partly molten. The composition can then be readily loaded into the desired container, the molten portion functioning as solvent or lubricant for the material still in solid form.
- the military explosive, amatol may be charged in the latter manner where the composition may be 40-80 parts ammonium nitrate and 60-20 parts trinitrotoluene.
- An object of the present invention is a high density blended explosive of uniform composition.
- a further object is a method of producing explosives of relatively high density under such conditions that the tendency toward segregation is eliminated.
- a still further object is such a method of producing high density blends of uniform composition containing ammonium nitrate and a normally solid sensitizing agent. AdditionaI objects will be disclosed as the invention is described more in detail hereinafter.
- blends comprising an inorganc oxidizing agent and a normally solid organic sensitizer therefor, first subjecting the blend to a temperature at which at least one of the above compounds is partly or entirely in molten condition. At the same time a compound is maintained in the blend capable of promotng dispersion of one of the two normally solid compounds in the molten portion of the second compound. The mixture is subsequently cooled and thereby solidified. The solidification to a firm mass may take place in any desired container, compacting being efiected by pressing, tamping, extruding, or by any suitable method.
- ammonium nitrate is a highly desirable inorganic oxidizing agent for use in the blends prepared according to our method, particularly because of the fact that it lends explosive strength to the mixture when properly primed. While it is essential to the invention that one of the ingredients of the blends be in a state of at least partial fusion during the preparation of the explosive, this molten compound may be either a normally solid organic sensitizer or the ammonium nitrate or other oxidizing agent, or other compound. Several variations of the invention are possible, according to the state in which the several ingredients are present.
- the ammonium nitrate is liquefied, while the organic sensitizer remains in the solid state. Since the normal fusion point of dry ammonium nitrate is above 169 C., it is essential in such a case to use with the ammonium nitrate a fusion point depressant, such as an inorganic nitrate or any compound organic or' inorganic which is soluble in molten nitrate, for example, water, urea, acetamid, dicyandiamid, guanidine, and the like. In this way. fusion may be brought about at temperatures between and C. Suitable sensitizing agents for blends thus prepared would be pentaerythritol tetranitrate, ammonium picrate, trinitronaphthalene, tetryl, trinitrobenzene and the like.
- a third embodiment we prepare the explosive by maintaining the ammonium nitrate in solid form throughout, while efi'ecting fusion of the organic sensitizer.
- the same sensitiz ing and dispersing agents are applicable here as in the previous case.
- Our preferred composition would fall in this class comprising ammonium nitrate and trinitrotoluene, which would be maintained at a temperaure between 80 and 100 C.
- inorganic oxidizing agents than ammonium nitrate may be employed under this third embodiment.
- compositions in which two organic compounds are included preferably two explosive compounds, in the absence of ammonium nitrate or other inorganic oxidizing agent.
- Such a composition may comprise trinitrotoluene, dinitrotoluene, or one of the lower nitronaphthalenes as a material of low fusion point, together with a higher melting compound having ordinarily not more than a limited solubility in the low-melting material.
- the preferred composition would be solid pentaerythritol tetranitrate dispersed in molten trinitrotoluene, for example in a 10430 ratio.
- this invention comprises a promotion of dispersion of one of the components of the blend throughout that component which is in molten form by means of a chemicalagent capable of furthering such dispersion.
- Various types of materials are suitable for this purpose taken from the group of compounds that fimction efl'ectively as surface-active agents, wetting agents, detergents, emulsifying materials, and the like.
- We may, for example, employ various higher fatty alcohol sulfates. for example, sodium lauryl sulfate and its mixtures with higher and lower homologs, various aliphatic and aromatic sulfonates such as sodium alkyl naphthalene sulfonates; fatty acid soaps, and the like.
- the dispersing agent may be one possessing no solubility for either of the ingredients, merely functioning as a wetting agent, or it may be one having some dissolving power for at least one of the ingredients.
- Example 1 The following composition was prepared and heated to a temperature of about 82 0.
- Example 3 Per cent Ammonium nitrate 79 Sodium acetate (anhydrous) 6 Trinitrotoluene 15
- Example 3 The'following composition was blended and heated to a temperature of around C. with addition of a dispersing agent similar to that used v in Examples 1 and 2.
- Example 4 A 65-35 blend of ammonium nitrate and trinitrotoluene was prepared and the trinitrotoluene content brought to fusion by subjection to a temperature of 65 C. When this blend was Poured in order to bring about solidification, separation of the fusible component resulted when no dispersion agent was used. The addition of either a sodium alkyl naphthalene sulfonste or a sodium sulfonate of an N-substituted oleic acid amide gave effective results in preventing separation. It will be realized that the use of the dispersing agent in the foregoing examples prevents the separation of two phases after pouring, and eliminates any necessity of vigorous and continuous stirring.
- the method of preparing relatively high density explosive compositions which comprises subjecting an inorganic oxidizing material and a normally solid organic sensitizer therefor to a temperature at which at least a portion of one of said compounds is in molten condition. maintaining in contacting relationship therewith a dispersing agent taken from the group consisting of sulfates of fatty alcohols, organic sulfonates and soaps of fatty acids, and subsequently cooling and solidifying the resulting blend.
- the method of preparing a blend of two normally solid nltrated organic compounds which comprises subjecting said compounds to a temperature at which at least a portion of one of said compounds is in molten condition, maintaining in contacting relationship therewith a dispersing agent taken from the group consisting of sulfates of fatty alcohols, organic sulfonates and soaps of fatty acids, and subsequently cooling and solidifying the resulting blend.
- the method of preparing a blend of ammonium nitrate and a normally solid organic sensitizer therefor which comprises subjecting said compounds to a temperature at which at least a portion of one of said compounds is in molten condition, maintaining in contacting relationship therewith a dispersing agent taken from the group consisting of sulfates of fatty alcohols, organic sulfonates and soaps of fatty acids, and subsequently cooling and solidifying the resulting blend.
- the method of blending ammonium nitrate and a normally solid organic sensitizer therefor which comprises subjecting ammonium nitrate, a fusion point depressant therefor, and said organic sensitizer to a temperature at which the ammonium nitrate becomes molten at least in part, while the organic compound remains in solid form, maintaining in contacting relationship therewith a dispersing agent taken from the group consisting of sulfates of fatty alcohols, organic sulfonates and soaps of fatty acids, and subsequently cooling and solidifying the resulting blend.
- the method of blending ammonium nitrate and a normally solid organic sensitizer therefor which comprises subjecting ammonium nitrate, a fusion point depressant, and said organic sensitizer to a temperature at which both the ammonium nitrate and the sensitizer become molten, at least in part, maintaining in contacting relationship therewith a dispersing agent taken from the group consisting of sulfates of fatty alcohols, organic sulfonates and soaps of fatty acids, and subsequently cooling and solidifying the resulting blend.
- the method of blending ammonium nitrate and a normally solid organic sensitizer therefor having a melting point below 100 C. which comprises subjecting ammonium nitrate and said organic sensitizer to a temperature at which the sensitizer becomes molten at least in part. while the ammonium nitrate remains unfused, maintaining in contacting relationship therewith a dispersing agent taken from the group consisting of sulfates of fatty alcohols, organic sulfonates and soaps of fatty acids, and subsequently cooling and solidifying the resulting blend.
- the method of blending ammonium nitrate and trinitrotoluene which comprises maintaining said compounds at a temperature between and C. in the presence of a compound selected from the group consisting of sulfates of fatty alcohols, organic sulfonates and soaps of fatty acids, and subsequently cooling and solidifying the resulting blend.
- a relatively high density explosive charge which comprises an inorganic oxidizing agent, a normally solid organic sensitizer therefor, and a compound selected from the group consisting of sulfates of fatty alcohols, organic sulfonates and soaps of fatty acids.
- a relatively high density explosive charge which comprises ammonium nitrate, a normally solid organic sensitizer therefor, and a compound selected from the group consisting of sulfates of fatty alcohols, organic sulfonates and soaps of fatty acids.
- a relatively high density explosive charge which comprises ammonium nitrate, trinitrotoluene, and a compound selected from the group consisting of sulfates of fatty alcohols, organic sulfonates and soaps of fatty acids.
- the method of preparing relatively high density explosive compositions which comprises subjecting two solid chemical compounds, at least i one of which is a nitrated organic compound, to a temperature at which at least a portion of one of said compounds is in molten condition, maintaining in contacting relationship therewith a dispersing agent taken from the group consisting of sulfates of fatty alcohols. organic sulfonates and soaps of fatty acids, and subsequently cooling and solidifying the resulting blend.
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Description
Patented July 11, 1944 2,353,147 HIGH-DENSITY EXPLOSIVE CHARGE Melvin A. Cook and Clyde 0. Davis, Woodbury, N. 1., assignors to E. I. du Pont de Nemours & Company, Wilmington, Del., a corporation of Delaware No Drawing. Application June 5, 1941,
Serial No. 396,655
Claims.
This invention relates to high density explosive charges and more particularly to methods of preparing such charges in a form adapted. to fill readily into containers.
High density is an essential characteristic "of many types of explosive charges since it permits the attainment of high, bull; strength. In shell charges for military use, for example, the highest density consistent with satisfactory initiating and propagating ability is desirable. Cast explosives representone efiective method of obtaining this result. A high density charge may be prepared by exposing a mixture of more than one compound of a predetermined blend to a temperature at which one of the compounds becomes at least partly molten. The composition can then be readily loaded into the desired container, the molten portion functioning as solvent or lubricant for the material still in solid form. The military explosive, amatol, may be charged in the latter manner where the composition may be 40-80 parts ammonium nitrate and 60-20 parts trinitrotoluene. While such a method can be carried out satisfactorily if suitable precautions of continuous and thorough mixing are taken, there is danger of segregation of the separate components when materials are used which are not mutually soluble. Such segregation would defeat the purpose of the careful blending and would cause a lack of uniformity in propagating power and dispersion of the composition.
An object of the present invention is a high density blended explosive of uniform composition. A further object is a method of producing explosives of relatively high density under such conditions that the tendency toward segregation is eliminated. A still further object is such a method of producing high density blends of uniform composition containing ammonium nitrate and a normally solid sensitizing agent. AdditionaI objects will be disclosed as the invention is described more in detail hereinafter.
We have found that the foregoing objects are attained and the disadvantages of the prior art overcome when we prepare blends comprising an inorganc oxidizing agent and a normally solid organic sensitizer therefor, first subjecting the blend to a temperature at which at least one of the above compounds is partly or entirely in molten condition. At the same time a compound is maintained in the blend capable of promotng dispersion of one of the two normally solid compounds in the molten portion of the second compound. The mixture is subsequently cooled and thereby solidified. The solidification to a firm mass may take place in any desired container, compacting being efiected by pressing, tamping, extruding, or by any suitable method.
- We find ammonium nitrate to be a highly desirable inorganic oxidizing agent for use in the blends prepared according to our method, particularly because of the fact that it lends explosive strength to the mixture when properly primed. While it is essential to the invention that one of the ingredients of the blends be in a state of at least partial fusion during the preparation of the explosive, this molten compound may be either a normally solid organic sensitizer or the ammonium nitrate or other oxidizing agent, or other compound. Several variations of the invention are possible, according to the state in which the several ingredients are present.
According to one embodiment, the ammonium nitrate is liquefied, while the organic sensitizer remains in the solid state. Since the normal fusion point of dry ammonium nitrate is above 169 C., it is essential in such a case to use with the ammonium nitrate a fusion point depressant, such as an inorganic nitrate or any compound organic or' inorganic which is soluble in molten nitrate, for example, water, urea, acetamid, dicyandiamid, guanidine, and the like. In this way. fusion may be brought about at temperatures between and C. Suitable sensitizing agents for blends thus prepared would be pentaerythritol tetranitrate, ammonium picrate, trinitronaphthalene, tetryl, trinitrobenzene and the like.
In another embodiment we prepare the blend by employing such compositions and conditions that both ammonium nitrate and organic sensitizer are in molten form. Again it would be essential to use a fusion point depressant for the ammonium nitrate. As sensitizing agent, organic materials having a melting point below 100' C. would preferably be used, for example, dinitrotoluene, trinitrotoluene, the lower nitronaphthalene, meta-dinitrobenzene, organic fuels such as diphenylamine, paraflln, and the like.
In a third embodiment we prepare the explosive by maintaining the ammonium nitrate in solid form throughout, while efi'ecting fusion of the organic sensitizer. The same sensitiz ing and dispersing agents are applicable here as in the previous case. Our preferred composition would fall in this class comprising ammonium nitrate and trinitrotoluene, which would be maintained at a temperaure between 80 and 100 C.
It will be understood that other inorganic oxidizing agents than ammonium nitrate may be employed under this third embodiment. We may use, for example, sodium nitrate, potassium nitrate, calcium nitrate, ammonium perchlorate, and the like. With such agents, the amount and type of sensitizer will have to be chosen to give the proper degree of sensitiveness to the finished explosive charge.
Our invention covers also compositions in which two organic compounds are included, preferably two explosive compounds, in the absence of ammonium nitrate or other inorganic oxidizing agent. Such a composition may comprise trinitrotoluene, dinitrotoluene, or one of the lower nitronaphthalenes as a material of low fusion point, together with a higher melting compound having ordinarily not more than a limited solubility in the low-melting material. The preferred composition would be solid pentaerythritol tetranitrate dispersed in molten trinitrotoluene, for example in a 10430 ratio.
As stated in the foregoing, this invention comprises a promotion of dispersion of one of the components of the blend throughout that component which is in molten form by means of a chemicalagent capable of furthering such dispersion. Various types of materials are suitable for this purpose taken from the group of compounds that fimction efl'ectively as surface-active agents, wetting agents, detergents, emulsifying materials, and the like. We may, for example, employ various higher fatty alcohol sulfates. for example, sodium lauryl sulfate and its mixtures with higher and lower homologs, various aliphatic and aromatic sulfonates such as sodium alkyl naphthalene sulfonates; fatty acid soaps, and the like. The dispersing agent may be one possessing no solubility for either of the ingredients, merely functioning as a wetting agent, or it may be one having some dissolving power for at least one of the ingredients.
The following examples will serve as specific embodiments for carrying out our invention:
Example 1 The following composition was prepared and heated to a temperature of about 82 0.
Per cent Ammonium nitrate 75 Sodium hyposulfite (hydrated)-.. 6 Trinitrotoluene 19 A small amount of a sodium alkyl naphthalene sulfonate was added, and the blend was agitated. The composition was introduced into a suitable container and tamped, using the above cooled and solidified composition in a container in di- Example 2 An explosive composition was prepared by heating the following blend to a temperature of around 85 0,
Per cent Ammonium nitrate 79 Sodium acetate (anhydrous) 6 Trinitrotoluene 15 Example 3 The'following composition was blended and heated to a temperature of around C. with addition of a dispersing agent similar to that used v in Examples 1 and 2.
Per cent Ammonium nitrate 74 Lead nitrah 5 Urea I Trinitrotoluene 13 The density of the solidified composition was 1.52, and a velocity of 3800 mJsec. was obtained. No segregation of components resulted.
Example 4 A 65-35 blend of ammonium nitrate and trinitrotoluene was prepared and the trinitrotoluene content brought to fusion by subjection to a temperature of 65 C. When this blend was Poured in order to bring about solidification, separation of the fusible component resulted when no dispersion agent was used. The addition of either a sodium alkyl naphthalene sulfonste or a sodium sulfonate of an N-substituted oleic acid amide gave effective results in preventing separation. It will be realized that the use of the dispersing agent in the foregoing examples prevents the separation of two phases after pouring, and eliminates any necessity of vigorous and continuous stirring.
Our invention has been disclosed at length in the foregoing but it will be apparent that many variations may be adopted in compositions, specific dispersing agents, and in procedures without departing from the scope of the invention. Weintend to be limited therefore only by the following patent claims: a
We claim:
1. The method of preparing relatively high density explosive compositions, which comprises subjecting an inorganic oxidizing material and a normally solid organic sensitizer therefor to a temperature at which at least a portion of one of said compounds is in molten condition. maintaining in contacting relationship therewith a dispersing agent taken from the group consisting of sulfates of fatty alcohols, organic sulfonates and soaps of fatty acids, and subsequently cooling and solidifying the resulting blend.
2. The method of preparing a blend of two normally solid nltrated organic compounds, which comprises subjecting said compounds to a temperature at which at least a portion of one of said compounds is in molten condition, maintaining in contacting relationship therewith a dispersing agent taken from the group consisting of sulfates of fatty alcohols, organic sulfonates and soaps of fatty acids, and subsequently cooling and solidifying the resulting blend.
3. The method of claim 2, in which a solid explosive compound is dispersed in molten trinitrotoluene.
4. The method of claim 2, in which pentaerythritol tetranitrate is dispersed in molten trinitrotoluene.
5., The method of preparing a blend of ammonium nitrate and a normally solid organic sensitizer therefor, which comprises subjecting said compounds to a temperature at which at least a portion of one of said compounds is in molten condition, maintaining in contacting relationship therewith a dispersing agent taken from the group consisting of sulfates of fatty alcohols, organic sulfonates and soaps of fatty acids, and subsequently cooling and solidifying the resulting blend.
6. The method of blending ammonium nitrate and a normally solid organic sensitizer therefor, which comprises subjecting ammonium nitrate, a fusion point depressant therefor, and said organic sensitizer to a temperature at which the ammonium nitrate becomes molten at least in part, while the organic compound remains in solid form, maintaining in contacting relationship therewith a dispersing agent taken from the group consisting of sulfates of fatty alcohols, organic sulfonates and soaps of fatty acids, and subsequently cooling and solidifying the resulting blend.
7. The method of claim 6, in which the solid organic sensitizer is pentaerythritol tetranitrate.
8. The method of blending ammonium nitrate and a normally solid organic sensitizer therefor, which comprises subjecting ammonium nitrate, a fusion point depressant, and said organic sensitizer to a temperature at which both the ammonium nitrate and the sensitizer become molten, at least in part, maintaining in contacting relationship therewith a dispersing agent taken from the group consisting of sulfates of fatty alcohols, organic sulfonates and soaps of fatty acids, and subsequently cooling and solidifying the resulting blend.
9. The method of claim 8, in which the solid organic sensitizer is trinitrotoluene.
.10. The method of blending ammonium nitrate and a normally solid organic sensitizer therefor having a melting point below 100 C., which comprises subjecting ammonium nitrate and said organic sensitizer to a temperature at which the sensitizer becomes molten at least in part. while the ammonium nitrate remains unfused, maintaining in contacting relationship therewith a dispersing agent taken from the group consisting of sulfates of fatty alcohols, organic sulfonates and soaps of fatty acids, and subsequently cooling and solidifying the resulting blend.
11. The method of blending ammonium nitrate and trinitrotoluene, which comprises maintaining said compounds at a temperature between and C. in the presence of a compound selected from the group consisting of sulfates of fatty alcohols, organic sulfonates and soaps of fatty acids, and subsequently cooling and solidifying the resulting blend.
12. A relatively high density explosive charge, which comprises an inorganic oxidizing agent, a normally solid organic sensitizer therefor, and a compound selected from the group consisting of sulfates of fatty alcohols, organic sulfonates and soaps of fatty acids.
13. A relatively high density explosive charge, which comprises ammonium nitrate, a normally solid organic sensitizer therefor, and a compound selected from the group consisting of sulfates of fatty alcohols, organic sulfonates and soaps of fatty acids.
14. A relatively high density explosive charge, which comprises ammonium nitrate, trinitrotoluene, and a compound selected from the group consisting of sulfates of fatty alcohols, organic sulfonates and soaps of fatty acids.
15. The method of preparing relatively high density explosive compositions which comprises subjecting two solid chemical compounds, at least i one of which is a nitrated organic compound, to a temperature at which at least a portion of one of said compounds is in molten condition, maintaining in contacting relationship therewith a dispersing agent taken from the group consisting of sulfates of fatty alcohols. organic sulfonates and soaps of fatty acids, and subsequently cooling and solidifying the resulting blend.
MELVIN A. COOK. CLYDE O. DAVIS.
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US396655A US2353147A (en) | 1941-06-05 | 1941-06-05 | High-density explosive charge |
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US396655A US2353147A (en) | 1941-06-05 | 1941-06-05 | High-density explosive charge |
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Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2425310A (en) * | 1943-04-28 | 1947-08-12 | Du Pont | Explosive |
US2429573A (en) * | 1945-06-18 | 1947-10-21 | Trojan Powder Co | Tetrapentaerythritol decanitrate and ammonium nitrate explosive |
US2455205A (en) * | 1945-08-24 | 1948-11-30 | Ici Ltd | Compositions suitable for use as gas and power producing liquids |
US2460375A (en) * | 1941-09-15 | 1949-02-01 | Ici Ltd | Granular or powder explosives and their manufacture |
US2482091A (en) * | 1944-03-20 | 1949-09-20 | Us Sec War | Method of making a high-density explosive |
US2499321A (en) * | 1946-08-24 | 1950-02-28 | Trojan Powder Co | Explosive composition |
US2548693A (en) * | 1945-08-24 | 1951-04-10 | Ici Ltd | Process of producing explosives containing ammonium nitrate |
US2817581A (en) * | 1955-05-18 | 1957-12-24 | Trojan Powder Co | Cast ammonium nitrate and urea explosive |
US2908560A (en) * | 1953-04-13 | 1959-10-13 | Dynamit Ag Vormals Alfred Nobe | Non-caking water-resistant explosive of the ammonium nitrate type |
US3053707A (en) * | 1957-06-11 | 1962-09-11 | Du Pont | Blasting agent |
US4009060A (en) * | 1975-09-12 | 1977-02-22 | Atlas Powder Company | Primer composition for use with explosive charges |
EP0493638A1 (en) * | 1990-12-31 | 1992-07-08 | Union Espanola De Explosivos S.A. | Novel composite explosives and method for making them |
US5486246A (en) * | 1994-09-15 | 1996-01-23 | Arcadian Fertilizer, L.P. | High density ammonium nitrate prill and method of production of the same |
US5527498A (en) * | 1994-09-15 | 1996-06-18 | Arcadian Fertilizer, L.P. | Method for production of high density ammonium nitrate prills |
FR2750131A1 (en) * | 1996-06-19 | 1997-12-26 | Giat Ind Sa | EXPLOSIVE COMPOSITION MELT / CASTABLE AND WITH REDUCED VULNERABILITY |
-
1941
- 1941-06-05 US US396655A patent/US2353147A/en not_active Expired - Lifetime
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2460375A (en) * | 1941-09-15 | 1949-02-01 | Ici Ltd | Granular or powder explosives and their manufacture |
US2425310A (en) * | 1943-04-28 | 1947-08-12 | Du Pont | Explosive |
US2482091A (en) * | 1944-03-20 | 1949-09-20 | Us Sec War | Method of making a high-density explosive |
US2429573A (en) * | 1945-06-18 | 1947-10-21 | Trojan Powder Co | Tetrapentaerythritol decanitrate and ammonium nitrate explosive |
US2455205A (en) * | 1945-08-24 | 1948-11-30 | Ici Ltd | Compositions suitable for use as gas and power producing liquids |
US2548693A (en) * | 1945-08-24 | 1951-04-10 | Ici Ltd | Process of producing explosives containing ammonium nitrate |
US2499321A (en) * | 1946-08-24 | 1950-02-28 | Trojan Powder Co | Explosive composition |
US2908560A (en) * | 1953-04-13 | 1959-10-13 | Dynamit Ag Vormals Alfred Nobe | Non-caking water-resistant explosive of the ammonium nitrate type |
US2817581A (en) * | 1955-05-18 | 1957-12-24 | Trojan Powder Co | Cast ammonium nitrate and urea explosive |
US3053707A (en) * | 1957-06-11 | 1962-09-11 | Du Pont | Blasting agent |
US4009060A (en) * | 1975-09-12 | 1977-02-22 | Atlas Powder Company | Primer composition for use with explosive charges |
EP0493638A1 (en) * | 1990-12-31 | 1992-07-08 | Union Espanola De Explosivos S.A. | Novel composite explosives and method for making them |
US5486246A (en) * | 1994-09-15 | 1996-01-23 | Arcadian Fertilizer, L.P. | High density ammonium nitrate prill and method of production of the same |
US5527498A (en) * | 1994-09-15 | 1996-06-18 | Arcadian Fertilizer, L.P. | Method for production of high density ammonium nitrate prills |
FR2750131A1 (en) * | 1996-06-19 | 1997-12-26 | Giat Ind Sa | EXPLOSIVE COMPOSITION MELT / CASTABLE AND WITH REDUCED VULNERABILITY |
EP0814069A1 (en) * | 1996-06-19 | 1997-12-29 | Giat Industries | Meltable/castable explosive composition with reduced sensitivity |
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