US1992217A - Ammonium nitrate explosive - Google Patents
Ammonium nitrate explosive Download PDFInfo
- Publication number
- US1992217A US1992217A US612383A US61238332A US1992217A US 1992217 A US1992217 A US 1992217A US 612383 A US612383 A US 612383A US 61238332 A US61238332 A US 61238332A US 1992217 A US1992217 A US 1992217A
- Authority
- US
- United States
- Prior art keywords
- explosive
- ammonium nitrate
- density
- sensitiveness
- detonation
- 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
Links
Classifications
-
- 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
- C06B31/28—Compositions containing an inorganic nitrogen-oxygen salt the salt being ammonium nitrate
- C06B31/32—Compositions containing an inorganic nitrogen-oxygen salt the salt being ammonium nitrate with a nitrated organic compound
- C06B31/38—Compositions containing an inorganic nitrogen-oxygen salt the salt being ammonium nitrate with a nitrated organic compound the nitrated compound being an aromatic
- C06B31/40—Compositions containing an inorganic nitrogen-oxygen salt the salt being ammonium nitrate with a nitrated organic compound the nitrated compound being an aromatic with an organic non-explosive or an organic non-thermic component
Definitions
- This invention relates to ammonium nitrate explosives and more particularly to such compositions having relatively low degrees of sensitiveness.
- the object of our invention is to provide explosives of increased safety because of their greatly reduced degree of sensitiveness.
- A. further object is such an explosive, containing ammonium nitrate as the principal ingredient.
- a still further object is to provide explosives of the kind described that cannot be exploded bythe ordinary blasting caps, but that can be used satisfactorily in many blasting operations when the point of view of potential strength and execution, it is too insensitive for use. Under such circumstances it would be dimcult to initiate, and,
- sensitizing materials we find various compounds available and satisfactory for use as such sensitizing materials, and we find it desirable to use a material capable of utilizing the excess oxygen of the ammonium nitrate, with thesimultaneous generation of heat thereby adding to the explosive effect.
- oxidizable inorganic elements or compounds for example aluminum, magnesium, selenium, sulphur, and inorganic sulphides, carbides, ferro-silicon or other silicides, and the like.
- organic fuels as sensitizing agent. In such.
- fuels containing oxygen for example, various alcohols such as amyl alcohol, ethylene glycol, glycerin and the like, aldehydes, ketones and carbohydrates, of which sugars, starch and cellulose are examples.
- fuels containing no oxygen and consisting of carbon or compounds of carbon and hydrogen.
- satisfactory fuels of this class we may cite various forms of carbon, hydrocarbons, and the like.
- coal as a fuel with ammonium nitrate.
- the ingredients of this mixture should be thoroughly incorporated so that there is intimate contact between the particles of the two ingredients.
- An additional class of compounds that give the desired results with ammonium nitrate is the one comprising the various nitro derivatives of the aromatic series.
- Many such nitrocompounds are available, having varying degrees of sensitiveness and sensitizing efiects. In general, it may be said that the greater the number of nitro groups and the higher the nitrogen content in such compounds, the greater is the sensitizing value.
- desirable mononitro compounds we may cite thederivatives of benzene, toluene, Xylene, naphthalene, phenol, and the like. Similarly, the dinitro derivatives of the same compounds may be used, and these will generally show a correspondinglygreater sensitizing value than the mononitro derivatives.
- the trinitroconipounds of the same materials have an even greater sensitizing eilfect, and under certain conditions these may impart to the explosive composition containing ammonium nitrate a sensitiveness greater than is desired. It may be so great, in fact, that the-explosive will be rendered sufficiently sensitive to detonate under the in-- fiuence of an ordinary commercial blasting cap, in which case the composition is outside the scope of our invention.
- compositions containing a nitrocompound of the aromatic series as. the sensitizer for ammonium nitrate we find the best results to be obtained by the use, with the nitrocompound, of an additional sensitizer consisting of a fuel or a material capable of utilizing the excess oxygen of the ammonium nitrate, with generation of heat.
- an additional sensitizer consisting of a fuel or a material capable of utilizing the excess oxygen of the ammonium nitrate, with generation of heat.
- various fuels may be chosen from those listed heretofore as satisfactory for use with ammonium nitrate, we prefer to employ an organic hydrocarbon, of which class the various aliphatic members of the paraflin and the olefin series .re represented as well as the aromatic hydrocarbons.
- we use the solid compound known as parafiin since this has the desired requisites of chemical and physical form and properties, and is economically available.
- the employment of the ingredients described in the preceding makes it possible to control the sensitiveness to the desired degree by various ad.- justments.
- the sensitiveness may be varied by the use of one or more diifererit nitrocompounds of varying degrees of nitration. It may be controlled, also, by varying the proportions of nitrocompound or compounds and parafiln hydrocarbon, since the hydrocarbon has a smaller sensitizingeffect than even a'monomtrocompound.
- a further very eflective means of adjusting the sensitiveness of'our explosive comprises the control of the fineness of the grains of ammonium nitrate employed. -For example, if ammonium nitrate is used.having a fineness such that over 50% will pass a 40-mesh screen, with at least 25% passing a IOO-mesh screen, the sensitiveness of the finished explosive, other things being equal, will be greater than if the finess is such that the greater part of the material is held on a 40-mesh screen.
- a less sensitive nitrocompound, or a relatively greater proportion of hydrocarbon to the amount of nitrocompound may be used than when the coarser grade is employed, while still obtaining the same sensitiveness in the finished explosive.
- the finer ammonium nitrate is used, a higher density explosive is possible with the same degree of sensitiveness for the finished explosive. Wider-variations in fineness than those just cited have a still greater effect on sensitiveness, and on the proportions and kinds of sensitizers necessary.
- the strength of the explosive may. be decreased
- the oxygen balance varied, by substitution for a portion of the ammonium nitrate of. sodium nitrate or other non-explosive oxidizing agent.
- compositions according to our invention 4 ammonium nitrate as the principal ingredienh'and inamounts of over 50%
- ammonium nitrate content will constitute more than 85% of the composition.
- the amounts of nitrocompounds oi the aromatic series and of paraffln hydrocarbon will vary according to the other factors involved, but will in all within the ranges of 0.5 to 10.0% for each of these ingredients. It the ammonium nitrate content ialls greatly below 85%, other explosive compounds may be used to make up the deficiency,
- the aim or mass of explosive should have a crossectional area preferably equal to or greater than that of a two-inch circle or about 3 square inches.
- This method involves the use of main charges of explosives having adegree of sensitiveness within defi'nitelimits. These limits state that the explosive, when unconfined, should be -incapable of detonation by means of a commercial No. 8 blasting cap, propagation when primed with 1,000 grams of trinitrotoluene as hereinafter described.
- the sensitiveness of the explosives may be determined according to the following test in which a single paperwrapped 4 x 8" cartridge of the explosive to be tested is placed vertically on a cylindrical lead test block, 2%" in diameter and 4" long, supported on asteel plate, and brought to detonation.
- the primer to be used has the same diameter as the explosive under .test, namely, 4%"
- the specific procedure consists in determining the minimum amountoi said primer, enclosed in a paper wrapper, which will cause the insensitive explosive under test to detonate and propagate consistently throughout the entire length of 8 inches and give a definite compression of the test block.
- the compression of the lead block Further? it isdesirable that an explosive be dim-- cases be but capable of detonation andv will vary greatly, and will depend both on the completeness of the propagation and on the velocity oi. detonation oi the tests explosive.
- the explosives covered by our invention are so regulated in sensitiveness that they do not require a sensitive primer throughout the entire length ofthe main explosive charge, and there! fore they constitute a definite improvement with respect to safety.
- Various so-called safety explosives with an ammonium nitrate base have been used in blasting, particularly in coal mining. As illustrations of such compositions maybe mentioned Bellite,
- a blasting explosive comprising 92 to 95% ammonium nitrate and 5 to 8% finely divided coal, the fineness and intimacy of contact of said constituents being so controlled that the detonation of the explosive and its propagation, when unconfined and at a density of 1.0, requires a detonating impulse substantially greater than that from any commercial detonator but not in excess of 1000 grams of TNT at a density of .95, said explosive having a cross-sectional area of at least about 3 square inches.
- the fineness of the ammonium-nitrate and the proportion of the nitrocompound to the oxidizable material being so controlled that the detonation of the explosive and its propagation, when unconfined and at a density of 1.0, requires a detonating impulse substantially greater than that from any commercial detonator but not in excess of 1000 grams oi TNT at a density 01' .95, said explosive having a cross-sectional area of at least about 3 square inches.
- plosive having a cross-sectional area of at least about 3 square inches.
- a blasting explosive containing more than 50% ammonium nitrate, at least one nitrocompound of the aromatic series, and a paraffin hydrocarbon, the fineness of the ammonium nitrate and the proportion of nitrocompound.to the hydrocarbon being so controlled that the detonation of the explosive and its propagation,
- said explosive having across-sectional area of not in excess of 1000 grams of TNT at a density of..'95, said explosive having a cross-sectional area of at least about 3 square inches.
- a blasting explosive according to claim 14 pulse substantially greater than that from any in which the ammonium nitrate used is of a commercial detonator but not in excess of 1000 fineness such that not less than 25% will pass grams of TNT at a density of .95, said explosive a IOU-mesh screen. having a cross-sectional area of at least about 3 WILLIAM EARLE KIRST. square inches. I I CLIFFORD A. WOODBURY.
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Organic Chemistry (AREA)
- Drilling And Exploitation, And Mining Machines And Methods (AREA)
- Working Measures On Existing Buildindgs (AREA)
- Air Bags (AREA)
Description
Patented Feb. 26,1935 I 992 217 2 umrso STATES PATENT OFFICE William Earle Kirst, Woodbury, N. 1.,
ford A. Woodbury, Media, Pa., du Pont de Nemours & Company, W Del., a corporation of Delaware amlClifassignorstoEL.
ilrnington,
No Drawing. .Application May 19, 1982, Serial No. 612,383
15 Claims.
This invention relates to ammonium nitrate explosives and more particularly to such compositions having relatively low degrees of sensitiveness. g
Commercial dynamites as manufactured heretofore. have been compounded so as to have a satisfactory in practical use. Their relatively high degree of sensitiveness, however, which makes it possible to detonate them'readily, carries with it some definite disadvantages. Such dynamites have, for example, a decided sensitiveness to shock and friction and certain ones are very inflammable, so that a definite and recognized hazard is involved in their manufacture, transportation and use. Explosives sumciently insensitive so that they are not capable of detonation by the ordinary means would have the advantage of increased safety in handling. This advantage would be of great practical value, particularly in quarry blasting, where large quantities of explosives are used in a single blast and. where the number of men involved is consider able.
In the copending application of W. E. Kirst, J. W. McCoy, and C. A. .Woodbury, Serial No. 599,592, filed March 1'7, 1932. a new method of blasting is described, involving the use of explosives capable of detonation by means of power.- ful booster charges but so insensitive that they cannot be detonated by ordinary means. It has been found that very insensitive explosives, especially in large diameters, can be made to propagate detonation with full emciency under the condition of confinement afforded by the bore hole, provided an adequate booster charge is used vforinitiating the explosive and that the degree of insensitiveness of the main explosive is regulated within definite limits.
The object of our invention is to provide explosives of increased safety because of their greatly reduced degree of sensitiveness. A. further object is such an explosive, containing ammonium nitrate as the principal ingredient. A still further object is to provide explosives of the kind described that cannot be exploded bythe ordinary blasting caps, but that can be used satisfactorily in many blasting operations when the point of view of potential strength and execution, it is too insensitive for use. Under such circumstances it would be dimcult to initiate, and,
in the diameters used in blasting work, would not propagate the explosion throughout the length of the column, even if initiation -were started. It is necessary, therefore, to employ one or more roperly chosen sensitizing agents with the ammonium nitrate.
We find various compounds available and satisfactory for use as such sensitizing materials, and we find it desirable to use a material capable of utilizing the excess oxygen of the ammonium nitrate, with thesimultaneous generation of heat thereby adding to the explosive effect. As such agents we may use oxidizable inorganic elements or compounds, for example aluminum, magnesium, selenium, sulphur, and inorganic sulphides, carbides, ferro-silicon or other silicides, and the like. We prefer, however, to employ organic fuels as sensitizing agent. In such. capacity, we may use fuels containing oxygen, for example, various alcohols such as amyl alcohol, ethylene glycol, glycerin and the like, aldehydes, ketones and carbohydrates, of which sugars, starch and cellulose are examples. We may use also fuels containing no oxygen, and consisting of carbon or compounds of carbon and hydrogen. As examples of satisfactory fuels of this class, we may cite various forms of carbon, hydrocarbons, and the like. We prefer, however, to use coal as a fuel with ammonium nitrate. We find a satisfactory composition to result when the relative proportions are selected of 92-95% ammonium nitrate and 5 -8 parts of coal. For such use, the ingredients of this mixture should be thoroughly incorporated so that there is intimate contact between the particles of the two ingredients.
An additional class of compounds that give the desired results with ammonium nitrate is the one comprising the various nitro derivatives of the aromatic series. Many such nitrocompounds are available, having varying degrees of sensitiveness and sensitizing efiects. In general, it may be said that the greater the number of nitro groups and the higher the nitrogen content in such compounds, the greater is the sensitizing value. As examples of desirable mononitro compounds, we may cite thederivatives of benzene, toluene, Xylene, naphthalene, phenol, and the like. Similarly, the dinitro derivatives of the same compounds may be used, and these will generally show a correspondinglygreater sensitizing value than the mononitro derivatives. The trinitroconipounds of the same materials have an even greater sensitizing eilfect, and under certain conditions these may impart to the explosive composition containing ammonium nitrate a sensitiveness greater than is desired. It may be so great, in fact, that the-explosive will be rendered sufficiently sensitive to detonate under the in-- fiuence of an ordinary commercial blasting cap, in which case the composition is outside the scope of our invention.
While any of the above mentioned nitrocompounds, and others which arenot named, are suitable for use, having varying contents of nitrogen, we find the nitrotoluenes the most generally satisfactory, and preferably use mononitrotoluene.
While desirable results are obtained by the use .of compositions containing a nitrocompound of the aromatic series as. the sensitizer for ammonium nitrate, we find the best results to be obtained by the use, with the nitrocompound, of an additional sensitizer consisting of a fuel or a material capable of utilizing the excess oxygen of the ammonium nitrate, with generation of heat. While various fuels may be chosen from those listed heretofore as satisfactory for use with ammonium nitrate, we prefer to employ an organic hydrocarbon, of which class the various aliphatic members of the paraflin and the olefin series .re represented as well as the aromatic hydrocarbons. Preferably, we use the solid compound known as parafiin, since this has the desired requisites of chemical and physical form and properties, and is economically available.
The employment of the ingredients described in the preceding makes it possible to control the sensitiveness to the desired degree by various ad.- justments. The sensitiveness may be varied by the use of one or more diifererit nitrocompounds of varying degrees of nitration. It may be controlled, also, by varying the proportions of nitrocompound or compounds and parafiln hydrocarbon, since the hydrocarbon has a smaller sensitizingeffect than even a'monomtrocompound.
A further very eflective means of adjusting the sensitiveness of'our explosive comprises the control of the fineness of the grains of ammonium nitrate employed. -For example, if ammonium nitrate is used.having a fineness such that over 50% will pass a 40-mesh screen, with at least 25% passing a IOO-mesh screen, the sensitiveness of the finished explosive, other things being equal, will be greater than if the finess is such that the greater part of the material is held on a 40-mesh screen. Using the finer grade ammonium nitrate just described, a less sensitive nitrocompound, or a relatively greater proportion of hydrocarbon to the amount of nitrocompound, may be used than when the coarser grade is employed, while still obtaining the same sensitiveness in the finished explosive. In a similar way, if the finer ammonium nitrate is used, a higher density explosive is possible with the same degree of sensitiveness for the finished explosive. Wider-variations in fineness than those just cited have a still greater effect on sensitiveness, and on the proportions and kinds of sensitizers necessary.
The strength of the explosive may. be decreased,
if desired, and the oxygen balance varied, by substitution for a portion of the ammonium nitrate of. sodium nitrate or other non-explosive oxidizing agent.
While the fineness of the ammonium nitrate has an important efiect on the sensitiveness of the explosive composition, an additional control- I II Per cent Per cent The foregoing compositions have different properties, depending on the several possible variables. Using a formula such as I, we prefer to pack it to a density of 1.15. Likewise, while various grades of ammonium nitrate may be used with respect to fineness, we preferably employ ammonium nitrate having afineness such that not more than 20% will be held on a 40-mesh screen, while not less than 25% will pass a 100-mesh screen. Under such conditions, when the explosive is properly primed and shot unconfined in cartridges, 5 inches in diameter and 16 inches in length, it will have a velocity approximating 5,000
meters per second. Its sensitiveness should be such that, when unconfined, it is incapable of detonation by a No. 8 blasting cap, but is capable of detonation by means of 1,000 grams of trinitrotoluene at a density of 0.95, or by various commercial explosives of high velocity in general use. As a matter of fact our explosive compositions will fail to detonate with several No. 8 caps fired simultaneously, or even a No. 9 or a No. 10 cap. It is apparent, therefore, that the sensitiveness of the composition is far below that necessary to detonate consistently with a single commercial blasting cap of maximum strength. Such an explosiveis entirely satisfactory, therefore, for use in commercial blasting operations, when primed by a suitable booster charge of high explosive.
It is known that the density of ammonium nitrate explosives has a considerable effect on the sensitiveness. 'For example, Marshall in his book on Explosives, v. I, p. 389, gives data showing this fact for an explosive comprising ammonium nitrate and 10% mononitronaphthalene. Whereas such an explosive at a density of 0.9 can be detonated by 0.4 grams of mercuryv fulminate, the same explosive at a density of 1.2 requires a charge of 5 grams of fulminate for its detonation. Our invention, however, does not comprise the control of thef sensitiveness of the explosive by variation of th density. We select the density desired for the explosive, depending on the bulk strength necessary, and bring about the properdegree of sensitiveness by adjustment of variables other than the density. Our explosive, for example, will be incapable of detonation' even by a No. 8 cap at densities of 1.0,
at which density the explosive cited by Marshall ftrate explosives rarely exceeds 1.0, except as the fulminate, which is the amount contained in the ordinary No. 6 blasting cap. The density of the majority of ammonium nis;expiosive is subjected to considerable pressure,
'will, in all cases, have of the finished explosive.
The compositions according to our invention 4 ammonium nitrate as the principal ingredienh'and inamounts of over 50% Preferably the ammonium nitrate content will constitute more than 85% of the composition. The amounts of nitrocompounds oi the aromatic series and of paraffln hydrocarbon will vary according to the other factors involved, but will in all within the ranges of 0.5 to 10.0% for each of these ingredients. It the ammonium nitrate content ialls greatly below 85%, other explosive compounds may be used to make up the deficiency,
Ior example one of the perchlorates. Such compounds, however, must not be present in amounts that will throw our explosive outside of the prescribed sensitiveness limits. Sodium nitrate may also be present under such conditions as a substitution for a portion of the ammonium nitrate,
with a corresponding reduction of the strength of the explosive.
The explosive compositions described in the foregoing are not adapted for use in blasting operations, except as they are employed in combination with a. booster charge of high explosive,
as described in the co-pending' application of Kirst, McCoy'and Woodbury, indicating that the aim or mass of explosive should have a crossectional area preferably equal to or greater than that of a two-inch circle or about 3 square inches.
This method involves the use of main charges of explosives having adegree of sensitiveness within defi'nitelimits. These limits state that the explosive, when unconfined, should be -incapable of detonation by means of a commercial No. 8 blasting cap, propagation when primed with 1,000 grams of trinitrotoluene as hereinafter described.
It has been found that explosives oi the above sensitiveness can be made to detonate and propagate continuously with full eiiiciency when loaded into drill holes and primed with one or more booster charges oi a more readily; detonated explosive, for example one of the higher grades of nitroglycerin or nitrostarch dynamites.
The sensitiveness of the explosives, according to our invention, may be determined according to the following test in which a single paperwrapped 4 x 8" cartridge of the explosive to be tested is placed vertically on a cylindrical lead test block, 2%" in diameter and 4" long, supported on asteel plate, and brought to detonation. The primer to be used has the same diameter as the explosive under .test, namely, 4%"
and consists of trinitrotoluene compressed to a density of 0.95. V
The specific procedure consists in determining the minimum amountoi said primer, enclosed in a paper wrapper, which will cause the insensitive explosive under test to detonate and propagate consistently throughout the entire length of 8 inches and give a definite compression of the test block. The compression of the lead block Further? it isdesirable that an explosive be dim-- cases be but capable of detonation andv will vary greatly, and will depend both on the completeness of the propagation and on the velocity oi. detonation oi the tests explosive. Using the above procedure, it is necessary that the explosive be brought to detonation and produce a dei'lnite compression by not more than 1,000 grams of trinitrotoluene, in order that'it. may fall, within the sensitiveness limits prescribed by our invention.
-'1'he same test procedure may be gmpldyed whendetermining the ability to detonate by means of a No. 8 cap, with the exception that the cap is inserted directly in the explosive.
We are aware that combinations oi ammonium nitrate with various sensitizing agents have been used as explosives heretofore. For example, the
well known Favier explosives described in U. S.
dense material, having a hollow core. The high density portion was so insensitive that it could not be made to detonate and propagate explosion with a contact primer at the end of a solid column, whatever the amount of primer. This made necessary the provision of a? centralcore which had to be filled with a cap-sensitive explosive, so that the entire length oi charge could be subjected to the influence of a powerful booster. The more sensitive explosive used by Favier for filling the hollow center and which detonated readily with an ordinary blasting'cap was therefore an essential part oi the whole explosive assembly, and the hazard connected with its use was determined by the sensitiveness of this more sensitive part.
The explosives covered by our invention are so regulated in sensitiveness that they do not require a sensitive primer throughout the entire length ofthe main explosive charge, and there! fore they constitute a definite improvement with respect to safety. 1 Various so-called safety explosives with an ammonium nitrate base have been used in blasting, particularly in coal mining. As illustrations of such compositions maybe mentioned Bellite,
their sensitiveness, therefore, these explosives are outside the scope of the present invention.
. While we havedescribed several embodiments in detail in the foregoing, other embodiments will now be apparent within the scope of our invention. It is, therefore, to-be understood that we do not intend to be limited in our invention except as indicated in the following patent claims.
We claim: 0
l. A blasting explosive containing ammonium nitrate as the principal ingredient and at least one sensitizing agent, the iineness and intimacy of contact of the constituents being so controlled thatthe detonation of the explosive and its propagation, when unconfined and at a density of 1.0, requires a detonating impulse substantially one sensitizing material capable of utilizing the excess oxygen of the ammonium nitrate with generation of heat, the fineness and intimacy of contact of the constituents being so controlled that the detonation of the explosive and its propagation, when unconfined and at a density of 1.0, requires a detonating impulse substantially greater than that from any commercial detonator but not in excess of 1000 grams of TNT at a density of .95, said explosive having a cross-sectional area of at least; about 3 square inches.
3. A blasting explosive containing ammonium nitrate as the principal ingredient and an organic fuel as sensitizing agent, the fineness and intimacy of contact of the constituents being so controlled that the detonation of the explosive and its propagation, when unconfined and at a density of 1.0, requires a detonating impulse substantially greater than that from any commercial detonator but not in excess of 1000 grams of TNT at a density of .95, said explosive having a crosssectional area of at least about 3 square inches.
4. A blasting explosive containing ammonium nitrate as the principal ingredient and finely divided coal as sensitizing agent, the fineness and intimacy of contact of said constituents being so -controlled that the detonation of the explosive and its propagation, when unconfined and at a density of 1.0, requires a detonating impulse substantially greater than that from any commercial detonator but not in excess of 1000 grams of TNT at a density of ..95, said explosive having a crosssectional area of at least about 3 square inches.
5. A blasting explosive comprising 92 to 95% ammonium nitrate and 5 to 8% finely divided coal, the fineness and intimacy of contact of said constituents being so controlled that the detonation of the explosive and its propagation, when unconfined and at a density of 1.0, requires a detonating impulse substantially greater than that from any commercial detonator but not in excess of 1000 grams of TNT at a density of .95, said explosive having a cross-sectional area of at least about 3 square inches.
6. A blasting explosive containing ammonium nitrate as the principal ingredient and at least one nitrocompound of the aromatic series, the fineness and intimacy of contact of the constituents and the sensitizing power of the nitrocompound being so controlled thatthe detonation of the explosive and its propagation, when unconfined and at a density of 1.0, requires a detonating impulse substantially greater than that from any commercial detonator but not in excess of 1000 grams of TNT at a density of .95, said explosive having a cross-sectional area of at least about 8 square inches.
7. A blasting explosive containing ammonium nitrate as the principal ingredient and mononitrotoluene as a sensitizing ingredient, the fineness and intimacy of contact of the constituents being so controlled that the detonation of the explosive and its propagation, when unconfined and at a density of 1.0, requires a detonating impulse substantially greater than that from any commercial detonator but not in excess of 1000 grams of TNT T at a density of .95, said explosive having a crosssectional area of at least about 3 square inches.
8. A blasting explosive containing more than 50% ammonium nitrate, at least one nitrocom-,
pound of the aromatic series, and a material capable of utilizingthe excess oxygen of the ammonium nitratewith generation of heat, the fineness of the ammonium-nitrate and the proportion of the nitrocompound to the oxidizable material being so controlled that the detonation of the explosive and its propagation, when unconfined and at a density of 1.0, requires a detonating impulse substantially greater than that from any commercial detonator but not in excess of 1000 grams oi TNT at a density 01' .95, said explosive having a cross-sectional area of at least about 3 square inches.
9. A blasting explosive containing more than 50% ammonium nitrate, at leastone nitrocompound of the aromatic series, and an organic fuel, the fineness of the ammonium nitrate and the proportion of nitrocompound to the fuel being so controlled that the detonation of theexplosive and its propagation, when unconfined and at a density of 1.0, requires a detonating impulse substantially greater thanthat from any commercial detonator but not in excess of 1000 grams of TNT at a density of .05, said explosive having a crosssectional area. of at least about 3 square inches.
I 10. A blasting explosive containing more than 50% ammonium nitrate, at least one nitrocompound of the aromatic series and a hydrocarbon, the fineness of the ammonium nitrate and the proportion of the nitrocompound to the hydrocarbo being so controlled that the detonation of the e plosive and its propagation, when uncon-' fined'and at a density of 1.0, requires a detonating impulse substantially greater than that from any commercial detonator but ,not in excess of 1000 grams of TNT at a density of .95, said ex-,
plosive having a cross-sectional area of at least about 3 square inches.
11. A blasting explosive containing more than 50% ammonium nitrate, at least one nitrocompound of the aromatic series, and a paraffin hydrocarbon, the fineness of the ammonium nitrate and the proportion of nitrocompound.to the hydrocarbon being so controlled that the detonation of the explosive and its propagation,
when unconfined and at a density of 1.0, requires a detonating impulse substantially greater. than that from any commercial detonator but riot in excess of 1000 grams of TNT at a density of .95,
said explosive having across-sectional area of not in excess of 1000 grams of TNT at a density of..'95, said explosive having a cross-sectional area of at least about 3 square inches.
13. A blasting explosive containing more than 50% ammonium nitrate, dinitrotoluene, and a 'parafiln hydrocarbon, the fineness of the ammonium nitrate and the proportion of dinitrotoluene to the hydrocarbon being so controlled that the detonation of the explosive and its propagation, when unconfined and at a density of 1.0, requires a detonating impulse substantially greater than that from any commercial detonator but not in excess of 1000 grams of TNT at a density of .95, said explosive having a crosssectional area of at least about 3square inches.
14. A blasting explosive containing more than 85% ammonium nitrate, 0.5 to 10.0% of at least one nitrated aromatic hydrocarbon, and 0.5 to 10.0% of a paramn hydrocarbon, the fineness oi the ammonium nitrate and the proportion of nitrated hydrocarbon, to parafiin hydrocarbon being so controlled that the detonation of the and at a density of 1.0, requires a detonating im- 15. A blasting explosive according to claim 14, pulse substantially greater than that from any in which the ammonium nitrate used is of a commercial detonator but not in excess of 1000 fineness such that not less than 25% will pass grams of TNT at a density of .95, said explosive a IOU-mesh screen. having a cross-sectional area of at least about 3 WILLIAM EARLE KIRST. square inches. I I CLIFFORD A. WOODBURY.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US612383A US1992217A (en) | 1932-05-19 | 1932-05-19 | Ammonium nitrate explosive |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US612383A US1992217A (en) | 1932-05-19 | 1932-05-19 | Ammonium nitrate explosive |
Publications (1)
Publication Number | Publication Date |
---|---|
US1992217A true US1992217A (en) | 1935-02-26 |
Family
ID=24452924
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US612383A Expired - Lifetime US1992217A (en) | 1932-05-19 | 1932-05-19 | Ammonium nitrate explosive |
Country Status (1)
Country | Link |
---|---|
US (1) | US1992217A (en) |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2577110A (en) * | 1947-10-23 | 1951-12-04 | Du Pont | Explosive composition containing vermiculite |
US2602732A (en) * | 1947-09-10 | 1952-07-08 | Atlas Powder Co | Ammonium nitrate explosive |
US2680068A (en) * | 1948-05-03 | 1954-06-01 | Ici Ltd | Ammonium nitrate blasting explosives |
US2752848A (en) * | 1953-02-19 | 1956-07-03 | Du Pont | Blasting explosive |
US2975046A (en) * | 1959-02-02 | 1961-03-14 | Spencer Chem Co | Ammonium nitrate explosive composition |
US3011883A (en) * | 1958-08-29 | 1961-12-05 | Du Pont | Dynamite composition |
US3032450A (en) * | 1958-04-01 | 1962-05-01 | Phillips Petroleum Co | Ammonium nitrate explosive and its production |
US3046887A (en) * | 1957-06-21 | 1962-07-31 | Consolidation Coal Co | Explosive system containing ammonium nitrate |
US3059575A (en) * | 1957-08-19 | 1962-10-23 | Trojan Powder Co | Seismographic exploration |
US3061488A (en) * | 1959-09-16 | 1962-10-30 | Jr Edwin M Scott | Explosive composition |
US3075464A (en) * | 1959-03-20 | 1963-01-29 | Reserve Mining Co | Blast hole charge and charging method |
US3094443A (en) * | 1963-06-18 | Table iv | ||
US3094069A (en) * | 1959-01-05 | 1963-06-18 | Dow Chemical Co | Method of blasting and ammonium nitrate explosive composition |
US3947301A (en) * | 1959-01-05 | 1976-03-30 | The Dow Chemical Company | Ammonium nitrate explosive composition |
-
1932
- 1932-05-19 US US612383A patent/US1992217A/en not_active Expired - Lifetime
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3094443A (en) * | 1963-06-18 | Table iv | ||
US2602732A (en) * | 1947-09-10 | 1952-07-08 | Atlas Powder Co | Ammonium nitrate explosive |
US2577110A (en) * | 1947-10-23 | 1951-12-04 | Du Pont | Explosive composition containing vermiculite |
US2680068A (en) * | 1948-05-03 | 1954-06-01 | Ici Ltd | Ammonium nitrate blasting explosives |
US2752848A (en) * | 1953-02-19 | 1956-07-03 | Du Pont | Blasting explosive |
US3046887A (en) * | 1957-06-21 | 1962-07-31 | Consolidation Coal Co | Explosive system containing ammonium nitrate |
US3059575A (en) * | 1957-08-19 | 1962-10-23 | Trojan Powder Co | Seismographic exploration |
US3032450A (en) * | 1958-04-01 | 1962-05-01 | Phillips Petroleum Co | Ammonium nitrate explosive and its production |
US3011883A (en) * | 1958-08-29 | 1961-12-05 | Du Pont | Dynamite composition |
US3094069A (en) * | 1959-01-05 | 1963-06-18 | Dow Chemical Co | Method of blasting and ammonium nitrate explosive composition |
US3947301A (en) * | 1959-01-05 | 1976-03-30 | The Dow Chemical Company | Ammonium nitrate explosive composition |
US2975046A (en) * | 1959-02-02 | 1961-03-14 | Spencer Chem Co | Ammonium nitrate explosive composition |
US3075464A (en) * | 1959-03-20 | 1963-01-29 | Reserve Mining Co | Blast hole charge and charging method |
US3061488A (en) * | 1959-09-16 | 1962-10-30 | Jr Edwin M Scott | Explosive composition |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4336085A (en) | Explosive composition with group VIII metal nitroso halide getter | |
US1992217A (en) | Ammonium nitrate explosive | |
US4304614A (en) | Zirconium hydride containing explosive composition | |
US2325064A (en) | Explosive composition | |
US4196026A (en) | Donor free radical explosive composition | |
US4142927A (en) | Free radical explosive composition | |
US4453989A (en) | Solid sensitizers for water-in-oil emulsion explosives | |
US2069612A (en) | Blasting explosive | |
US2124201A (en) | Explosive composition and process of production | |
US2975046A (en) | Ammonium nitrate explosive composition | |
AU615595B2 (en) | Nitroalkane-based emulsion explosive composition | |
US2107157A (en) | Explosive | |
US4664729A (en) | Water-in-oil explosive emulsion composition | |
US1992216A (en) | Method of blasting | |
US3201291A (en) | Dispersion-type blasting explosives | |
US2312752A (en) | Explosive composition | |
US4764229A (en) | Sensitization of inorganic oxidizer explosives | |
US3579392A (en) | Nitroglycerin-nitroglycol blasting composition | |
US2033198A (en) | Explosive | |
US5608184A (en) | Alternative use of military propellants as novel blasting agents | |
US3166451A (en) | Sensitizing agents comprising the reaction product of urea-formaldehyde-hydrogen peroxide | |
AU625503B2 (en) | High emulsifier content explosives | |
US2314809A (en) | Explosive composition | |
US3044912A (en) | Ammonium nitrate-cyanide explosive | |
US2185248A (en) | Ammonium nitrate explosive |