US2736262A - Low density safety ammonium nitrate - Google Patents

Low density safety ammonium nitrate Download PDF

Info

Publication number
US2736262A
US2736262A US2736262DA US2736262A US 2736262 A US2736262 A US 2736262A US 2736262D A US2736262D A US 2736262DA US 2736262 A US2736262 A US 2736262A
Authority
US
United States
Prior art keywords
ammonium nitrate
sodium chloride
low density
density
composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Publication date
Application granted granted Critical
Publication of US2736262A publication Critical patent/US2736262A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B23/00Compositions characterised by non-explosive or non-thermic constituents
    • C06B23/02Compositions characterised by non-explosive or non-thermic constituents for neutralising poisonous gases from explosives produced during blasting
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S102/00Ammunition and explosives
    • Y10S102/704Coolants

Definitions

  • low density powder blasting explosives the low density characteristics are ordinarily attained by the use in the composition of a dried vegetable carbohydrate constituent that is itself of unusually low density characteristics even in its comminuted form, for instance balsa woodmeal, ground cork, bagasse or certain low density peat preparations. It is also the custom in the manufacture of these explosives to employ forms of ammonium nitrate of a low range of bulk density; but it is nevertheless a matter of inconvenience or difliculty to obtain a low density ammonium nitrate safety blasting explosive of a desirable composition.
  • ammonium nitrate in special forms of exceptionally low bulk density to assist the attainment of a low density ammonium nitrate safety blasting explosive composition
  • exceptionally low density forms of ammonium nitrate are composed of hollow crystal clusters of a fragile nature and because of their fragility or changes in crystal form on storage, especially under moist conditions, dililculty may be experienced in transporting them undamaged to the site of the explosive manufacture, or the crystal clusters may tend to break up in the resulting explosive composition on storage or transport.
  • sodium chloride as a flame-quenching constituent in safety blasting explosives is well known and hitherto the sodium chloride employed has been in the form of a well dried relatively fine powder of high bulk density, that is to say about 1.2 to 1.3 gms./cc.'at 1.7 atmospheres pressure.
  • Such material can be obtained directly by evaporation of brine in a vacuum evaporation apparatus or by grinding coarser material such as open pan grades of salt.
  • a low density safety ammonium nitrate blasting powder explosive composition of the kind including sodium chloride as a flame-quenching ingredient is characterized in that the sodium chloride included has a bulk density not exceeding 0.9 gm./cc. at 1.7 atmospheres pressure.
  • sodium chloride of said bulk density permits said powder explosives to be obtained of lower bulk density for a given composition, or permits smaller quantities of low density vegetable carbohydrate material to be employed and consequently enables the oxygen deficiency of the detonation gases to be minimized, or the amount of 2 v sodium nitrate or the like salt of high oxidizing value in the explosive composition to be minimized andhence enables the proportion of flame-quenching salt to be increased with obvious advantage to its safety characteristics, or renders it possible to employ forms of ammonium nitrate of more convenient bulk density in the explosive composition.
  • Low density sodium chloride suitable for the carrying out of the present invention may be formed by rapidly adding potassium nitrate to a boiling solution of equimolecular proportions of sodium nitrate and potassium chloride saturated with respect to the resulting sodium chloride.
  • dendritic forms of sodium chloride by which we mean crystal clusters with 'at least three main spiky or needle shaped arms lying in'more than one plane, in some cases with subsidiary arms growing from the main arms.
  • dendritic crystals of this kind having a pouring density not exceeding 0.7 gm./cc., which corresponds to a packing density under 1.7 atmospheres pressure of approximately 0.8 gm./ cc.
  • sodium chloride Unlike ammonium nitrate, sodium chloride has no crystal transition point at 323 C. or indeed at any temperature, and its density characteristics, unlike those of ammonium nitrate, are not liable to variation when stored even under slightly moist conditions.
  • Example I A low density powder explosive composition consisting of- Per cent :20 mixture of nitroglycerine and ethyleneglycol dinitrate 10 Peat (of bulk density 0.20 gm./cc. under a packing pressure of 1.7 atmospheres) l2 Ammonium nitrate (of bulk density 0.71 gnu/cc.
  • the sodium chloride used consists of dendritic crystals
  • S. S. screen is prepared by mixing the ingredients together in known manner in an Atlas mixer.
  • the resulting powder explosive composition has a bulk density of 0.63 gm./cc. under a packing pressure of 1.7 atmospheres.
  • the explosive is cartridged to a density of 0.62 gm./cc. into cartridges of 32 mm. diameter and 200 mm. long.
  • the power is 59% of that of blasting gelatine.
  • the velocity of detonation is 1450 metres per second.
  • the oxygen deficiency is 1.4 gm. oxygen per 100 gm. of unwrapped explosive.
  • a comparative powder explosive composition not in accordance with the invention is prepared wherein the method employed is the same and the composition is the same except that the sodium chloride is ordinary vacuum dried material consisting of cubicle crystals of bulk density 1.3 gm./cc. at 1.7 atmospheres pressure whereof all pass a 30 mesh, 86% passes a 60 mesh and 57% passes a 100 mesh B. S. S. screen.
  • the bulk density of the resulting powder explosive composition is 0.72 gm./cc. at 1.7 atmospheres and when cartridged under the same conditions as the composition made in accordance with the invention "the cartridge density is 0.67 gm./cc.
  • the velocity of detonation is 1500 metres per second.
  • the oxygen deficiency is 1.4 gum/100 gm. of unwrapped explosive.
  • the dendritic salt in the explosive powder composition prepared according to the invention is replaced by salt ofthe same bulk density prepared by rapidly adding potassium nitrate to a boiling solution of equimolecular proportions of sodium nitrate and potassium chloride saturated with respect to the resulting sodium chloride an explosive powder composition is obtained having a bulk density of 0.63 gm./cc. under a packing pressure of 1.7 atmospheres.
  • Example II A powder explosive composition having the same explosive properties as the powder explosive compositions described in Example I can be produced by raising respectively the percentages of dendritic sodium chloride and ammonium nitrate to 14% and 65%, by reducing the peat content to and by omitting the sodium nitrate.
  • the resulting explosive composition has a bulk density of 0.65 :gm./cc. under 1.7 atmospheres pressure and when cartridged to a density of 0.70 gm./cc. its velocity of detonation is 1600 metres per second. Its power as measured in the ballistic mortar is 62% of that of blasting gelatine, and the oxygen deficiency is 1.4 gm./ 100 gm. of unwrapped explosive.
  • Example III -A powder explosive composition is prepared by the same manner of mixing and having the same composition as the powder explosive of Example 1 except that the percentage of peat is reduced to 10% and the percentage of ammonium nitrate is increased to 57.5%.
  • the resulting powder explosive composition has a bulk density of 0.68 gm./cc. at 1.7 atmospheres pressure and has an oxygen excess of 1.8 gm./ 100 gm. of unwrapped explosive.
  • Example IV A powder explosive composition is prepared as described in Example I except that the percentage of peat and the ammonium nitrate are reduced to 7% and 45% and the percentage of dendritic salt is increased to 37.5%.
  • the bulk density of the resulting powder explosive composition is 0.78 gm./cc. at 1.7 atmospheres pressure and when cartridged to a density of 0.75 gm./ cc. its velocity of detonation is 1450 metres per second.
  • the power is 39% of that of blasting gelatine and the oxygen deficiency is 1.4 gm./100 gm. of unwrapped explosive.
  • Example V For comparison purposes two powder explosive compositions each consisting of Per cent 80:20 mixture of nitroglycerine and ethylene glycol dinitrate 10 Peat (of bulk density 0.20 gm./cc. under a packing pressure of 1.7 atmospheres) 12 Ammonium nitrate 55.5 Sodium nitrate 10 4 Sodium chloride 12 Diammonium hydrogen phosphate 0.2 Natural resin 0.3
  • ammonium nitrate is of bulk density 0.82 gm./ cc. under a packing pressure of 1.7 atmospheres and the sodium chloride is of bulk density of 0.82-gmjcc. at 1.7 atmospheres pressure and the other not according to the invention wherein the ammonium nitrate is of bulk density of 0.71 gm./cc. under a packing pressure of 1.7 atmospheres and the sodium chloride is of bulk density 1.3 gm./ cc. at 1.7 atmospheres pressure.
  • the two powder explosive compositions are each cartridged to a density of 0.68 gm./ cc.
  • the explosive properties of the two powder compositions are substantially the same but whereas a 227 gm. cartridge of the composition not in accordance with the invention when suspended in a methane-air mixture containing 9% methane by volume ignites the atmosphere when initiated by a No. 6 mercury fulminate-chlora'te electric detonator having a copper alloy casing, in contradistinction thereto a similar cartridge having the powder composition prepared according to the invention tested under these conditions does not ignite such an atmosphere.
  • a process as claimed in claim 3 wherein the sodium chloride comprises dendritic crystals and has a packing density-of about 0.8 g./cc. under 1.7 atmospheres pressure.

Description

United States atent Low DENSITY SAFETY ONIUM NITRATE BLASTING EXPLOSIVE AND PROCESS non PRO- DUCING SAME James Taylor, Saltcoats, Scotland, assignor to Imperial vChemical Industries Limited, a corporation of Great Britain No Drawing. Application March 5, 1951, Serial No. 214,029
Claims priority, application Great Britain March 29, 1950 5 Claims. (Cl. 102-24) The present invention relates to improvements in low density safety ammonium nitrate blasting explosive compositions of powder consistency of the kind comprising sodium chloride as a flame-quenching ingredient.
In the manufacture of low density powder blasting explosives the low density characteristics are ordinarily attained by the use in the composition of a dried vegetable carbohydrate constituent that is itself of unusually low density characteristics even in its comminuted form, for instance balsa woodmeal, ground cork, bagasse or certain low density peat preparations. It is also the custom in the manufacture of these explosives to employ forms of ammonium nitrate of a low range of bulk density; but it is nevertheless a matter of inconvenience or difliculty to obtain a low density ammonium nitrate safety blasting explosive of a desirable composition.
Thus the employment of a relatively high proportion of the low density vegetable carbohydrate ingredient has the disadvantage that it will necessitate the simultaneous employment of a correspondingly high proportion of an oxidizing salt of high available oxygen content, usually sodium nitrate, which has the effect of limiting the proportion of the flame-quenching ingredient that can be used in the composition. It is also known to employ ammonium nitrate in special forms of exceptionally low bulk density to assist the attainment of a low density ammonium nitrate safety blasting explosive composition, but exceptionally low density forms of ammonium nitrate are composed of hollow crystal clusters of a fragile nature and because of their fragility or changes in crystal form on storage, especially under moist conditions, dililculty may be experienced in transporting them undamaged to the site of the explosive manufacture, or the crystal clusters may tend to break up in the resulting explosive composition on storage or transport.
The use of sodium chloride as a flame-quenching constituent in safety blasting explosives is well known and hitherto the sodium chloride employed has been in the form of a well dried relatively fine powder of high bulk density, that is to say about 1.2 to 1.3 gms./cc.'at 1.7 atmospheres pressure. Such material can be obtained directly by evaporation of brine in a vacuum evaporation apparatus or by grinding coarser material such as open pan grades of salt.
According to the present invention a low density safety ammonium nitrate blasting powder explosive composition of the kind including sodium chloride as a flame-quenching ingredient is characterized in that the sodium chloride included has a bulk density not exceeding 0.9 gm./cc. at 1.7 atmospheres pressure.
The use of sodium chloride of said bulk density permits said powder explosives to be obtained of lower bulk density for a given composition, or permits smaller quantities of low density vegetable carbohydrate material to be employed and consequently enables the oxygen deficiency of the detonation gases to be minimized, or the amount of 2 v sodium nitrate or the like salt of high oxidizing value in the explosive composition to be minimized andhence enables the proportion of flame-quenching salt to be increased with obvious advantage to its safety characteristics, or renders it possible to employ forms of ammonium nitrate of more convenient bulk density in the explosive composition. a
Low density sodium chloride suitable for the carrying out of the present invention may be formed by rapidly adding potassium nitrate to a boiling solution of equimolecular proportions of sodium nitrate and potassium chloride saturated with respect to the resulting sodium chloride.
There may also be employed dendritic forms of sodium chloride by which we mean crystal clusters with 'at least three main spiky or needle shaped arms lying in'more than one plane, in some cases with subsidiary arms growing from the main arms. In co-pending application Serial No. 140,143, filed January 23, 1950, now Patent No. 2,642,335 there are claimed dendritic crystals of this kind having a pouring density not exceeding 0.7 gm./cc., which corresponds to a packing density under 1.7 atmospheres pressure of approximately 0.8 gm./ cc.
Unlike ammonium nitrate, sodium chloride has no crystal transition point at 323 C. or indeed at any temperature, and its density characteristics, unlike those of ammonium nitrate, are not liable to variation when stored even under slightly moist conditions. a
The invention is illustrated in the following examples in which the parts and percentages are by weight except where otherwise indicated.
Example I A low density powder explosive composition consisting of- Per cent :20 mixture of nitroglycerine and ethyleneglycol dinitrate 10 Peat (of bulk density 0.20 gm./cc. under a packing pressure of 1.7 atmospheres) l2 Ammonium nitrate (of bulk density 0.71 gnu/cc.
under a packing pressure of 1.7 atmospheres).. 55.5 Sodium nitrate vl0 Sodium chloride 12. Diammonium hydrogen phosphate 0.2 Natural resin 0.3
in which the sodium chloride used consists of dendritic crystals, has a bulk density of 0.82 gm./cc. at 1.7 atmospheres pressure and of which 98% passes a 30 mesh, 48% passes a 60 mesh and 16% passes a 100 mesh B. S. S. screen, is prepared by mixing the ingredients together in known manner in an Atlas mixer. The resulting powder explosive composition has a bulk density of 0.63 gm./cc. under a packing pressure of 1.7 atmospheres. The explosive is cartridged to a density of 0.62 gm./cc. into cartridges of 32 mm. diameter and 200 mm. long. The power is 59% of that of blasting gelatine. The velocity of detonation is 1450 metres per second. The oxygen deficiency is 1.4 gm. oxygen per 100 gm. of unwrapped explosive.
A comparative powder explosive composition not in accordance with the invention is prepared wherein the method employed is the same and the composition is the same except that the sodium chloride is ordinary vacuum dried material consisting of cubicle crystals of bulk density 1.3 gm./cc. at 1.7 atmospheres pressure whereof all pass a 30 mesh, 86% passes a 60 mesh and 57% passes a 100 mesh B. S. S. screen. The bulk density of the resulting powder explosive composition is 0.72 gm./cc. at 1.7 atmospheres and when cartridged under the same conditions as the composition made in accordance with the invention "the cartridge density is 0.67 gm./cc. The velocity of detonation is 1500 metres per second. The oxygen deficiency is 1.4 gum/100 gm. of unwrapped explosive.
If the dendritic salt in the explosive powder composition prepared according to the invention is replaced by salt ofthe same bulk density prepared by rapidly adding potassium nitrate to a boiling solution of equimolecular proportions of sodium nitrate and potassium chloride saturated with respect to the resulting sodium chloride an explosive powder composition is obtained having a bulk density of 0.63 gm./cc. under a packing pressure of 1.7 atmospheres.
Example II A powder explosive composition having the same explosive properties as the powder explosive compositions described in Example I can be produced by raising respectively the percentages of dendritic sodium chloride and ammonium nitrate to 14% and 65%, by reducing the peat content to and by omitting the sodium nitrate. The resulting explosive composition has a bulk density of 0.65 :gm./cc. under 1.7 atmospheres pressure and when cartridged to a density of 0.70 gm./cc. its velocity of detonation is 1600 metres per second. Its power as measured in the ballistic mortar is 62% of that of blasting gelatine, and the oxygen deficiency is 1.4 gm./ 100 gm. of unwrapped explosive.
Example III -A powder explosive composition is prepared by the same manner of mixing and having the same composition as the powder explosive of Example 1 except that the percentage of peat is reduced to 10% and the percentage of ammonium nitrate is increased to 57.5%. The resulting powder explosive composition has a bulk density of 0.68 gm./cc. at 1.7 atmospheres pressure and has an oxygen excess of 1.8 gm./ 100 gm. of unwrapped explosive.
Example IV A powder explosive composition is prepared as described in Example I except that the percentage of peat and the ammonium nitrate are reduced to 7% and 45% and the percentage of dendritic salt is increased to 37.5%. The bulk density of the resulting powder explosive composition is 0.78 gm./cc. at 1.7 atmospheres pressure and when cartridged to a density of 0.75 gm./ cc. its velocity of detonation is 1450 metres per second. The power is 39% of that of blasting gelatine and the oxygen deficiency is 1.4 gm./100 gm. of unwrapped explosive.
Example V For comparison purposes two powder explosive compositions each consisting of Per cent 80:20 mixture of nitroglycerine and ethylene glycol dinitrate 10 Peat (of bulk density 0.20 gm./cc. under a packing pressure of 1.7 atmospheres) 12 Ammonium nitrate 55.5 Sodium nitrate 10 4 Sodium chloride 12 Diammonium hydrogen phosphate 0.2 Natural resin 0.3
and each having a bulk density of 0.68 gm./cc. at 1.7 atmospheres pressure are prepared, one according to the invention wherein the ammonium nitrate is of bulk density 0.82 gm./ cc. under a packing pressure of 1.7 atmospheres and the sodium chloride is of bulk density of 0.82-gmjcc. at 1.7 atmospheres pressure and the other not according to the invention wherein the ammonium nitrate is of bulk density of 0.71 gm./cc. under a packing pressure of 1.7 atmospheres and the sodium chloride is of bulk density 1.3 gm./ cc. at 1.7 atmospheres pressure.
The two powder explosive compositions are each cartridged to a density of 0.68 gm./ cc.
The explosive properties of the two powder compositions are substantially the same but whereas a 227 gm. cartridge of the composition not in accordance with the invention when suspended in a methane-air mixture containing 9% methane by volume ignites the atmosphere when initiated by a No. 6 mercury fulminate-chlora'te electric detonator having a copper alloy casing, in contradistinction thereto a similar cartridge having the powder composition prepared according to the invention tested under these conditions does not ignite such an atmosphere.
What I claim is:
1. A low density safety ammonium nitrate blasting powder explosive composition of the kind including sodium chloride as the sole flame-quenching ingredient characterized in that the sodium chloride is dendritic and has a bulk density not exceeding 0.9 gm./cc. at 1.7 atmospheres pressure.
2. A low density safety ammonium nitrate blasting powder explosive composition as claimed in claim '1 wherein the sodium chloride comprises dendritic crystals and has a packing density of about 0.8 g./cc. under 1.7 atmospheres pressure.
3. In a process for the production of a low density safety ammonium nitrate blasting powder explosive'composition, the step of adding to said composition dendritic sodium chloride having a density not exceeding 0.9 g./ cc. at 1.7 atmospheres pressure as the sole flame-quenching ingredient.
4. A process as claimed in claim 3 wherein the sodium chloride comprises dendritic crystals and has a packing density-of about 0.8 g./cc. under 1.7 atmospheres pressure.
5. A blasting cartridge containing a low density safety ammonium nitrate blasting powder explosive composition including dendritic sodium chloride having a bulk density not exceeding 0.9 g./cc. at 1.7 atmospheres pressure as the sole flame-quenching ingredient.
References Cited in the file of this patent UNITED STATES PATENTS 2,087,285 Handforth et a1 July 20, 1937 FOREIGN PATENTS 595,443 Great Britain Dec. 4, 1947

Claims (3)

1. A LOW DENSITY SAFETY AMMONIUM NITRATE BLASTING POWDER EXPLOSIVE COMPOSITION OF THE KIND INCLUDING SODIUM CHLORIDE AS THE SOLE FLAME-QUENCHING INGREDIENT CHARACTERIZED IN THAT THE SODIUM CHLORIDE IS DENDRITIC AND HAS A BULK DENSITY NOT EXCEEDING 0.9 GM./CC. AT 1.7 ATMOSPHERES PRESSURE.
3. IN A PROCESS FOR THE PRODUCTION OF A LOW DENSITY SAFETY AMMONIUM NITRATE BLASTING POWDER EXPLOSIVE COMPOSITION, THE STEP OF ADDING TO SAID COMPOSITION DENDRITIC SODIUM CHLORIDE HAVING A DENSITY NOT EXCEEDING 0.9 G./CC. AT 1.7 ATMOSPHERES PRESSURE AS THE SOLE FLAME-QUENCHING INGREDIENT.
5. A BLASTING CARTRIDGE CONTAINING A LOW DENSITY SAFETY AMMONIUM NITRATE BLASTING POWDER EXPLOSIVE COMPOSITION INCLUDING DENDRITIC SODIUM CHLLORIDE HAVING A BULK DENSITY NOT EXCEEDING 0.9 G./CC. AT 1.7 ATMOSPHERES PRESSURE AS THE SOLE FLAME-QUENCHING INGREDIENT.
US2736262D 1950-03-29 Low density safety ammonium nitrate Expired - Lifetime US2736262A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB7836/50A GB682209A (en) 1950-03-29 1950-03-29 Improvements in or relating to low density safety ammonium nitrate blasting explosives

Publications (1)

Publication Number Publication Date
US2736262A true US2736262A (en) 1956-02-28

Family

ID=9840704

Family Applications (1)

Application Number Title Priority Date Filing Date
US2736262D Expired - Lifetime US2736262A (en) 1950-03-29 Low density safety ammonium nitrate

Country Status (4)

Country Link
US (1) US2736262A (en)
DE (1) DE915196C (en)
GB (1) GB682209A (en)
NL (2) NL159892B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3356546A (en) * 1963-12-30 1967-12-05 Ici Ltd Safety blasting composition with a metal formate as a fuel
US4912813A (en) * 1987-03-06 1990-04-03 Eisen- Und Drahtwerk Erlau Aktiengesellschaft Belt connection mechanism

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2087285A (en) * 1935-01-10 1937-07-20 Du Pont Ammonium nitrate explosive
GB595443A (en) * 1945-07-09 1947-12-04 Edward Whitworth Improvements in or relating to low density blasting explosives

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2087285A (en) * 1935-01-10 1937-07-20 Du Pont Ammonium nitrate explosive
GB595443A (en) * 1945-07-09 1947-12-04 Edward Whitworth Improvements in or relating to low density blasting explosives

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3356546A (en) * 1963-12-30 1967-12-05 Ici Ltd Safety blasting composition with a metal formate as a fuel
US4912813A (en) * 1987-03-06 1990-04-03 Eisen- Und Drahtwerk Erlau Aktiengesellschaft Belt connection mechanism

Also Published As

Publication number Publication date
NL82333C (en)
NL159892B (en)
DE915196C (en) 1954-08-16
GB682209A (en) 1952-11-05

Similar Documents

Publication Publication Date Title
US4997496A (en) Explosive and propellant composition and method
US3153606A (en) Aqueous explosive composition containing flake aluminum and ammonium nitrate
US2736262A (en) Low density safety ammonium nitrate
US3361604A (en) Explosive slurries containing an inorganic oxidizer salt and particulate fibrous naturally wet pulpy plant matter
US3047441A (en) Hydrogen peroxide explosives
US3102834A (en) Composition comprising nitrocellulose, nitroglycerin and oxides of lead or copper
US2548693A (en) Process of producing explosives containing ammonium nitrate
US2589703A (en) Lead styphnate and process of manufacturing same
US2709130A (en) Blasting explosives
US2613146A (en) Unsheathed safety explosive composition
US4096003A (en) Aluminum, amine nitrate sensitized gel explosive compositions
US3344005A (en) Pentaerythritol tetranitrate-trimethylolethane trinitrate explosives
US2125161A (en) Ammonium nitrate explosive
US1979681A (en) Explosive
US2481795A (en) Explosives suitable for safety blasting explosives
US3296042A (en) Explosive containing oxidizing salt, organic nitro-compound, and hydrophilic colloid
US2055403A (en) Explosive
US1778718A (en) Gelignite and gelatin dynamite
US3580753A (en) Tmetn-inorganic nitrate explosives blended with aluminum
US1985968A (en) Explosive
US3668027A (en) Method of making nitrocellulose-nitroglycerine water-bearing explosive compositions
US3235424A (en) High density water-containing blasting materials containing ferrosilicon and ammonium nitrate
US1905289A (en) Explosive
US2759807A (en) Gelatinous explosive compositions
US2131574A (en) Explosive