US2992912A - Ammonium nitrate explosive composition - Google Patents
Ammonium nitrate explosive composition Download PDFInfo
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- US2992912A US2992912A US2992912DA US2992912A US 2992912 A US2992912 A US 2992912A US 2992912D A US2992912D A US 2992912DA US 2992912 A US2992912 A US 2992912A
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- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 title claims description 51
- 239000000203 mixture Substances 0.000 title claims description 49
- 239000002360 explosive Substances 0.000 title claims description 26
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 16
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 13
- 229910052799 carbon Inorganic materials 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 229910021529 ammonia Inorganic materials 0.000 claims description 7
- 229920006395 saturated elastomer Polymers 0.000 claims description 5
- XLYOFNOQVPJJNP-PWCQTSIFSA-N Tritiated water Chemical compound [3H]O[3H] XLYOFNOQVPJJNP-PWCQTSIFSA-N 0.000 claims 1
- 238000005422 blasting Methods 0.000 description 7
- 239000003337 fertilizer Substances 0.000 description 7
- 229920000591 gum Polymers 0.000 description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
- 239000003999 initiator Substances 0.000 description 6
- 239000002562 thickening agent Substances 0.000 description 6
- 210000002445 nipple Anatomy 0.000 description 5
- 230000000717 retained effect Effects 0.000 description 5
- 239000006229 carbon black Substances 0.000 description 4
- 238000005474 detonation Methods 0.000 description 4
- 238000010304 firing Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- 239000004576 sand Substances 0.000 description 4
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 230000035939 shock Effects 0.000 description 3
- UBLAMKHIFZBBSS-UHFFFAOYSA-N 3-Methylbutyl pentanoate Chemical compound CCCCC(=O)OCCC(C)C UBLAMKHIFZBBSS-UHFFFAOYSA-N 0.000 description 2
- 235000007173 Abies balsamea Nutrition 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- 239000004857 Balsam Substances 0.000 description 2
- 241000206575 Chondrus crispus Species 0.000 description 2
- 229920002907 Guar gum Polymers 0.000 description 2
- 229920000569 Gum karaya Polymers 0.000 description 2
- 244000018716 Impatiens biflora Species 0.000 description 2
- 239000004233 Indanthrene blue RS Substances 0.000 description 2
- 239000005909 Kieselgur Substances 0.000 description 2
- 240000005546 Piper methysticum Species 0.000 description 2
- 235000016787 Piper methysticum Nutrition 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000000665 guar gum Substances 0.000 description 2
- 235000010417 guar gum Nutrition 0.000 description 2
- 229960002154 guar gum Drugs 0.000 description 2
- 230000000977 initiatory effect Effects 0.000 description 2
- 235000010494 karaya gum Nutrition 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 239000006193 liquid solution Substances 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 241000948470 Amanita phalloides Species 0.000 description 1
- 241000416162 Astragalus gummifer Species 0.000 description 1
- 235000014698 Brassica juncea var multisecta Nutrition 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 241001310324 Cetraria islandica Species 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 229920000161 Locust bean gum Polymers 0.000 description 1
- 229920003091 Methocel™ Polymers 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- 241000364021 Tulsa Species 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 244000275904 brauner Senf Species 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000006233 lamp black Substances 0.000 description 1
- 235000010420 locust bean gum Nutrition 0.000 description 1
- 239000000711 locust bean gum Substances 0.000 description 1
- 238000005065 mining Methods 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- -1 polyethylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 238000005029 sieve analysis Methods 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B25/00—Compositions containing a nitrated organic compound
- C06B25/34—Compositions containing a nitrated organic compound the compound being a nitrated acyclic, alicyclic or heterocyclic amine
Definitions
- This invention relates to an improved ammonium nitrate explosive composition and more particularly concerns an ammoniacal ammonium nitrate explosive composition containing carbon as a sensitizer. It has been a desideratum in the explosives art to formulate and compound explosive compositions which may be handled and transported with relative safety yet reliably and effectively detonated. To fill this need various ammonium nitrate explosive compositions have been proposed but these have generally contained materials that are quite shock sensitive or the compositions have required boosters such as gelatin dynamite spaced throughout a large load to insure good provocation,
- Another object of the invention is to provide an ammonium nitrate explosive composition in the form of a paste or slurry whereby a charge of the composition upon being loaded into a rigid or flexible container, or directly into a bore hole, contains a minimum of void spaces within the charge.
- Another object of the invention is to provide an ammonium nitrate explosive composition containing a sensitizer which is not adversely affected by moisture during storage of the composition.
- An additional object of the invention is to provide an ammonium nitrate explosive composition containing carbon as a sensitize'r.
- a still further object of the invention is to provide a low cost ammonium nitrate explosive composition which is adapted to be readily compounded near the point of use.
- composition of the invention may be compounded with fertilizer grade as well as explosive grade ammonium nitrate. While the explosive grade material tends to detonate with slightly greater force on an equal Weight basis it is generally more economical to make up for this by using a slightly greater amount of fertilizer grade ammonium nitrate.
- Fertilizer grade ammonium nitrate generally contains various additives or fine particulate coatings inhibiting caking and promoting free-flowing characteristics of the material.
- Ammonium nitrate as referred to herein is defined as ammonium nitrate containing up to 3 percent of various additives such as wax, diatomaceous earth and chalk, in addition to a moisture content-ranging up to about 1% percent, either the granular or prilled form of the nitrate salt are satisfactory.
- composition is best prepared from ammonium nitrate having particle sizes mainly in the range of 8 to 100 mesh, fines passing 100 to 200 mesh tending to increase the sensitivity of the mixture.
- ammonium nitrate having particle sizes mainly in the range of 8 to 100 mesh, fines passing 100 to 200 mesh tending to increase the sensitivity of the mixture.
- An example of a satisfactory granular ammonium nitrate readily obtained commercially has the following sieve analysis:
- Carbon in the form of finely ground coke, charcoal or coal as well as carbon black or lamp black is suitable for use in compounding the composition of the invention.
- Fine particulate carbon passing a 325 mesh sieve is to be preferred though carbon having particle sizes up to that retained on a 60 mesh sieve may be used if desired.
- Coarse particulate carbon tends to react slower during a detonation and is thus less efliciently use.
- a suitable ammoniacal solution of ammonium nitrate is Divers liquid which is a saturated or nearly saturated anhydrous solution of ammonium nitrate in liquid ammonia containing generally about 60 to 80 percent of ammonium nitrate.
- a similar ammom'acal solution of ammonium nitrate containing in addition up to 15 percent of water is referred to herein as an ammoniacal solution of ammonium nitrate.
- Such aqueous ammoniacal solutions are commercially available at lower cost and are easier to handle than the anhydrous Divers liquid because of the reduced vapor pressure of the ammonia therein in the presence of water.
- a solution consisting of 60 percent of ammonium nitrate, 34 percent of liquid ammonia and 6 percent of water is commercially available.
- the hereinabove described components of the explosive mixture of the invention may be combined in various proportions ranging from 6 to percent of solid particulate ammonium nitrate, from 0.5 to 20 percent of finely divided carbon and from about 3 to 87 percent of an ammoniacal solution of ammonium nitrate containing up to 30 percent of water and substantially saturated with respect to ammonium nitrate. It is to be understood that while compositions in this range, will, under room temperature conditions, contain both dissolved ammonium nitrate and solid phase particulate ammonium nitrate in the proportions described, the relative amount of ammonium nitrate in each phase is determined by the temperature and pressure of the mixture under equilibrium conditions. At higher temperatures under a constant pressure more solid particulate ammonium nitrate will be taken up by the solution and at lower temperatures a lesser amount. For this reason the invention has been defined above with respect to mixtures equilibrated at room temperature and under atmospheric pressure.
- the proportions range from 60 to about 97 percent of ammonium nitrate total, from 0.5 to 20 percent of finely divided carbon, from 1 to 30 percent of ammonia and up to 3 percent of water.
- Mixtures of the invention containing less than about 18 to 20 percent of liquid solution phase are generally in the form of a lumpy paste and are advantageously loaded into accessible bore holes or placed in suitable containers which may be charged into a bore hole as in mining or quarrying operations.
- Mixtures of the invention containing more than about 20 percent of the liquid solution phase are to be preferred for pumping into a bore hole as a slurry and are especially advantageously used in loading an elongated horizontal or upwardly sloping bore hole.
- the explosive composition of the invention may be thickened upon admixing therewith from about 0.12 to 5 percent, based on the Weight of the liquid phase, of a thickening agent such as methyil cellulose or gum karaya.
- a thickening agent such as methyil cellulose or gum karaya.
- suitable thickening agents are carboxymethyl cellulose, kava-kava gum, guar gum, accroides gum, locust bean gum, gum tragacanth, balsam tolu natural, gum bezoin Sumatra, Irish moss, Iceland moss and Separan NP-IO (a high molecular weight polyacrylarnide).
- the ingredients of the composition are mixed together in small quantities as by kneading in a plastic bag or in larger quantities as with a mechanical agitator or paddle mixer.
- a load or charge of the so prepared mixture is placed in the desired location, usually in the confinement of a bore hole.
- a shaped charge such as a commercially available jet perforator containing a charge of RDX is armed with a suitable initiator such as a No. 8 blasting cap and placed next to the load.
- the shaped charge is oriented with respect to the explosive load so that the firing access is directed toward the load, preferably its mid-point.
- the electrical lead for the blasting cap is rigged to a time controlled firing mechanism or run to a remote control device and, if desired, a sand or gravel tamp is placed over the load and initiator. The load is then fired upon setting off the blasting cap and shaped charge.
- ammonium nitrate explosive mixture of the invention various embodiments of the invention were compared and tested.
- a 10 pound quantity of explosive mixture was formulated of a particulated fertilizer grade of ammonium nitrate, finely divided carbon black and ammonia, or of a particulated fertilizer grade ammonium nitrate, finely divided carbon black and an aqueous ammoniacal solution of ammonium nitrate known as Spensol D in the proportions and amount shown hereinbelow in Table IV.
- the individual proportions were in each case mixed in a separate polyethylene plastic bag of suflicient size 'to readily hold the quantity prepared.
- the various components of the mixture were weighed into the bag, the bag closed and the contents mixed together by kneading the bag with the hands.
- the fertilizer grade of ammonium ntirate contained about 0.7 percent of wax, 1 percent of diatomaceous earth and 0.3 percent of chalk.
- the particle size of the ammonium nitrate was such that 94 percent by weight of the particles passed a 20 mesh sieve and percent by weight were retained on a mesh sieve.
- the carbon was in the form of carbon black.
- the prepared mixtures were loaded into individual shallow bore holes drilled in clay soil and having a diameter of 4 inches and depth of about 4 feet. Successive bore holes were spaced about 20 feet apart.
- the loading of each hole was accomplished by first placing an initiator in the form of a shaped charge armed with a blasting cap in the bottom of the hole and running the lead wires from the blasting cap to a firing control switch. Each shaped charge used was positioned with the jet end or firm'g axis facing upwardly.
- the explosive mixtures, contained in the plastic bags in which they were mixed, were dumped into respective test holes, the bags in each case deforming over the initiator. Sand was used as a tamp, the hole being filled from the bag to ground level 'with sand.
- composition of the invention with conventional explosives varied amounts of 60 percent dynamite each with a No. 8 electric blasting cap therefore were placed in shallow test holes 4 feet deep, tamped with sand and detonated. 5 pounds of dynamite so loaded and detonated produced a crater 5 feet in diameter and 1.5 feet deep; 10 pounds of dynamite produced a crater 8 feet in diameter and 1 foot deep; while 25 pounds of dynamite produced a crater 11 feet in dimeter and 5 feet deep.
- composition of the invention containing from 60 to 80 percent of ammonium nitrate is efiectively detonated by a shaped charge under the conditions of the test.
- compositions of the invention possess the advantage that they may be slurried in an additional amount of an ammoniacal solution of ammonium nitrate and pumped into a bore hole and there allowed to settle out to form a detonable composition.
- An ammonium nitrate explosive composition consisting essentially of particulate ammonium nitrate in admixture with from 0.5 to 20 percent by weight of finely divided carbon and with an ammoniacal solution which is substantially saturated with respect to ammonium nitrate, said ammoniacal solution containing a proportion of ammonia equivalent to from 1 to percent by weight of the total weight of the admixture, said ammoniacal solution further containing up to 30 percent by weight of water, but the said water not exceeding 3 percent of 30 percent by weight of water based on the weight of the ammoniacal solution, the said Water not exceeding 3 percent by weight of the total weight of the admixture, said ammoniacal solution having a proportion of ammonia equivalent to from about 5 to 15 percent by weight of the total weight of the admixture and said admixture containing a combined total in all phases of at least percent by weight of ammonium nitrate.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Fertilizers (AREA)
Description
United States Patent 2,992,912 AMMONIUM NITRATE EXPLOSIVE COMPOSITION Joseph R. Hradel, Mount Pleasant, Mich., and Harold E. Staadt, Tulsa, Okla, assignors to The Dow Chemical Company, Midland, Mich, a corporation of Delaware No Drawing. Filed Jan. 5, 1959, Ser. No. 784,867 4 Claims. ('CI. 52-14) This invention relates to an improved ammonium nitrate explosive composition and more particularly concerns an ammoniacal ammonium nitrate explosive composition containing carbon as a sensitizer. It has been a desideratum in the explosives art to formulate and compound explosive compositions which may be handled and transported with relative safety yet reliably and effectively detonated. To fill this need various ammonium nitrate explosive compositions have been proposed but these have generally contained materials that are quite shock sensitive or the compositions have required boosters such as gelatin dynamite spaced throughout a large load to insure good provocation,
It is an object of the present invention to provide an ammonium nitrate explosive composition which may be safely handled and transported with little danger of shock initiation yet may be detonated eifectively by a shaped charge using the Monroe jet principle. 7
It is another object of the invention to provide an ammonium nitrate explosive composition of moderate shock sensitivity which yet upon proper initiation produces a detonation of useful magnitude and force.
Another object of the invention is to provide an ammonium nitrate explosive composition in the form of a paste or slurry whereby a charge of the composition upon being loaded into a rigid or flexible container, or directly into a bore hole, contains a minimum of void spaces within the charge.
Another object of the invention is to provide an ammonium nitrate explosive composition containing a sensitizer which is not adversely affected by moisture during storage of the composition.
An additional object of the invention is to provide an ammonium nitrate explosive composition containing carbon as a sensitize'r.
A still further object of the invention is to provide a low cost ammonium nitrate explosive composition which is adapted to be readily compounded near the point of use.
Other objects and advantages of the invention will become apparent to one skilled in the art upon becoming familiar with the following description and claims.
These and other objects are attained upon admixing ammonium nitrate, itself cap insensitive, with a carbon sensitizer and with 'an ammoniacal solution of ammonium nitrate in proportions hereinafter more fully described and further illustrated by examples of the invention. All proportions herein given in percent are to be understood as percent by weight unless otherwise indicated.
The composition of the invention may be compounded with fertilizer grade as well as explosive grade ammonium nitrate. While the explosive grade material tends to detonate with slightly greater force on an equal Weight basis it is generally more economical to make up for this by using a slightly greater amount of fertilizer grade ammonium nitrate.
Fertilizer grade ammonium nitrate generally contains various additives or fine particulate coatings inhibiting caking and promoting free-flowing characteristics of the material. Ammonium nitrate as referred to herein is defined as ammonium nitrate containing up to 3 percent of various additives such as wax, diatomaceous earth and chalk, in addition to a moisture content-ranging up to about 1% percent, either the granular or prilled form of the nitrate salt are satisfactory.
To avoid making cap sensitive mixtures the composition is best prepared from ammonium nitrate having particle sizes mainly in the range of 8 to 100 mesh, fines passing 100 to 200 mesh tending to increase the sensitivity of the mixture. An example of a satisfactory granular ammonium nitrate readily obtained commercially has the following sieve analysis:
Table I Number Number Percent of sieve 1 of sieve re retained passed tamed on 12 0.3 12 20 34. 4 20 30 16. 4 30 40 13.4 40 60 14. 4 60 8. 4 80 100 1.9 100 200 6. 4 200 Pan 4. 4
Table 11 Number Number of sieve of sieve Percent passed retained retained 6 0 6 10 56 10 12 24 12 14 9 14 20 9 20 35 2 35 Pan Tr.
The above examples are not intended to limitative but indicative of the nature of commercially available am-, monium nitrate.
Carbon in the form of finely ground coke, charcoal or coal as well as carbon black or lamp black is suitable for use in compounding the composition of the invention. Fine particulate carbon passing a 325 mesh sieve is to be preferred though carbon having particle sizes up to that retained on a 60 mesh sieve may be used if desired. Coarse particulate carbon tends to react slower during a detonation and is thus less efliciently use.
A suitable ammoniacal solution of ammonium nitrate is Divers liquid which is a saturated or nearly saturated anhydrous solution of ammonium nitrate in liquid ammonia containing generally about 60 to 80 percent of ammonium nitrate. A similar ammom'acal solution of ammonium nitrate containing in addition up to 15 percent of water is referred to herein as an ammoniacal solution of ammonium nitrate. Such aqueous ammoniacal solutions are commercially available at lower cost and are easier to handle than the anhydrous Divers liquid because of the reduced vapor pressure of the ammonia therein in the presence of water. As an example, a solution consisting of 60 percent of ammonium nitrate, 34 percent of liquid ammonia and 6 percent of water is commercially available.
The hereinabove described components of the explosive mixture of the invention may be combined in various proportions ranging from 6 to percent of solid particulate ammonium nitrate, from 0.5 to 20 percent of finely divided carbon and from about 3 to 87 percent of an ammoniacal solution of ammonium nitrate containing up to 30 percent of water and substantially saturated with respect to ammonium nitrate. It is to be understood that while compositions in this range, will, under room temperature conditions, contain both dissolved ammonium nitrate and solid phase particulate ammonium nitrate in the proportions described, the relative amount of ammonium nitrate in each phase is determined by the temperature and pressure of the mixture under equilibrium conditions. At higher temperatures under a constant pressure more solid particulate ammonium nitrate will be taken up by the solution and at lower temperatures a lesser amount. For this reason the invention has been defined above with respect to mixtures equilibrated at room temperature and under atmospheric pressure.
In another manner of defining the explosive composition of the invention, that is, in terms of the individual molecular or elemental species from which the composition may be prepared if desired, the proportions range from 60 to about 97 percent of ammonium nitrate total, from 0.5 to 20 percent of finely divided carbon, from 1 to 30 percent of ammonia and up to 3 percent of water.
Mixtures of the invention containing less than about 18 to 20 percent of liquid solution phase are generally in the form of a lumpy paste and are advantageously loaded into accessible bore holes or placed in suitable containers which may be charged into a bore hole as in mining or quarrying operations.
Mixtures of the invention containing more than about 20 percent of the liquid solution phase are to be preferred for pumping into a bore hole as a slurry and are especially advantageously used in loading an elongated horizontal or upwardly sloping bore hole.
If desired, the explosive composition of the invention may be thickened upon admixing therewith from about 0.12 to 5 percent, based on the Weight of the liquid phase, of a thickening agent such as methyil cellulose or gum karaya. Other suitable thickening agents are carboxymethyl cellulose, kava-kava gum, guar gum, accroides gum, locust bean gum, gum tragacanth, balsam tolu natural, gum bezoin Sumatra, Irish moss, Iceland moss and Separan NP-IO (a high molecular weight polyacrylarnide). The effects of various thickening agents on the viscosity respectively, of Divers liquid and of an aqueous ammoniacal solution also known as Spensol D, a trademarked product, and containing 60'peroent of ammonium nitrate, 34 percent of ammonia and 6 percent of water were determined and the results are listed in Table HI.
Table III Viscosity of ammoniacal solution after addition Weight of thickener (cps) Thickener percent of thickener Diver's Spensol D liquid 5 100, 000 100, 000 Guar gum 5 41 100, 000 Kava kava gum 5 450 Accroides gum 120 1100111350 bean gum 13 o 100, 000 Balsam tolu natural gum- 20 Irish moss 60 Iceland moss- 42 Separan NP 10. 140 Methocel HG...-. Do 19 77 315 95, 000 18 28 5 142 1 395 5 84, 000 4, 000
' In preparing and detonating the composition of the invention the ingredients of the composition are mixed together in small quantities as by kneading in a plastic bag or in larger quantities as with a mechanical agitator or paddle mixer. A load or charge of the so prepared mixture is placed in the desired location, usually in the confinement of a bore hole. A shaped charge, such as a commercially available jet perforator containing a charge of RDX is armed with a suitable initiator such as a No. 8 blasting cap and placed next to the load. The shaped charge is oriented with respect to the explosive load so that the firing access is directed toward the load, preferably its mid-point. The electrical lead for the blasting cap is rigged to a time controlled firing mechanism or run to a remote control device and, if desired, a sand or gravel tamp is placed over the load and initiator. The load is then fired upon setting off the blasting cap and shaped charge.
To demonstrate the properties of the ammonium nitrate explosive mixture of the invention various embodiments of the invention were compared and tested. In each test a 10 pound quantity of explosive mixture was formulated of a particulated fertilizer grade of ammonium nitrate, finely divided carbon black and ammonia, or of a particulated fertilizer grade ammonium nitrate, finely divided carbon black and an aqueous ammoniacal solution of ammonium nitrate known as Spensol D in the proportions and amount shown hereinbelow in Table IV. The individual proportions were in each case mixed in a separate polyethylene plastic bag of suflicient size 'to readily hold the quantity prepared. The various components of the mixture were weighed into the bag, the bag closed and the contents mixed together by kneading the bag with the hands. The fertilizer grade of ammonium ntirate contained about 0.7 percent of wax, 1 percent of diatomaceous earth and 0.3 percent of chalk. The particle size of the ammonium nitrate was such that 94 percent by weight of the particles passed a 20 mesh sieve and percent by weight were retained on a mesh sieve. The carbon was in the form of carbon black.
The prepared mixtures were loaded into individual shallow bore holes drilled in clay soil and having a diameter of 4 inches and depth of about 4 feet. Successive bore holes were spaced about 20 feet apart. The loading of each hole was accomplished by first placing an initiator in the form of a shaped charge armed with a blasting cap in the bottom of the hole and running the lead wires from the blasting cap to a firing control switch. Each shaped charge used was positioned with the jet end or firm'g axis facing upwardly. The explosive mixtures, contained in the plastic bags in which they were mixed, were dumped into respective test holes, the bags in each case deforming over the initiator. Sand was used as a tamp, the hole being filled from the bag to ground level 'with sand. Detonation of the mixture was attempted by closing the firing switch thus setting off the initiator at the bottom of the hole. The magnitudes of the detonations obtained were determined by measuring the size of the crater produced. While the crater size alone is not indicative of the amount of earch formation that is broken up or loosened, it does give an indication of. the work potential of the mixture detonated. The crater size herein reported shows how much material was thrown sufiiciently so as not to fall back over the test hole. Test conditions and results are summarized in Table IV.
In order to compare the composition of the invention with conventional explosives varied amounts of 60 percent dynamite each with a No. 8 electric blasting cap therefore were placed in shallow test holes 4 feet deep, tamped with sand and detonated. 5 pounds of dynamite so loaded and detonated produced a crater 5 feet in diameter and 1.5 feet deep; 10 pounds of dynamite produced a crater 8 feet in diameter and 1 foot deep; while 25 pounds of dynamite produced a crater 11 feet in dimeter and 5 feet deep.
n In another test series additional embodiments of the invention were compounded. Each mixture was used to entirely fill a 3 inch x 12 inch steel pipe nipple which was capped on both ends and laid on the ground. The change was initiated by a shaped charge containing 3.25 oz. of RDX which Was positioned at one end of the nipple so as to tire longitudinally into the nipple. In one such test the steel pipe nipple was heated by electrical resistance heating elements and the contents of the nipple subjected to hydrolic pressure.
The compositions tested and the results obtained are summarized in Table V.
Table IV Composition Initiator Crater dfinensions,
Gum Weight Test No. Kaof load, Weight raya lbs. Blasting RDX in Diam- FGAN NHa S.D. cap shaped eter Depth charge, oz.
89 6 1O 8 EB O 1 8 2. 94 1 8 EBO 1 5 5 81 4 l0 8 EBO 1 6 2 94 1 10 8 E130 l 9 1 84 1 10 8 EBO 1 9 1 78 2 l0 8 EBO 1 9 1 87 3 10 8 EBO 1 9. 5 1. 5 80 1O 8 EBO 1 8 6 75 5 10 8 EBO 1 6 Heaved. 85 13 34 10 8 EBO 3. 25 7 4 85 10 y 10 8 EBO 3. 25 7 4 90 s i 10 8 E30 3. 25 s 4. a 97 2 54 10 8 EBO 3. 25 8 4 80 10 34 10 8 EBO 3. 25 10 5 85 5 V 10 8 EBC 3. 25 12 6 93 4 10 8 E130 3. 25 12 6 96 2 x 10 8 EBC 3. 25 12 6 84 3 $4 10 8 EEC 3.25 10 5 70 15 $4 10 8 EBO 3. 25 8 6 73 $4 10 8 EBO 3. 10 6 EGAN-fertilizer grade ammonium. S.D.Spensol D RDX-trimethyiene trinitramme.
1 Percent based on weight of liquid phase at room temperature.
a commercial aqueous ammoniacal solution of ammonium nitrate.
The results show that a composition of the invention containing from 60 to 80 percent of ammonium nitrate is efiectively detonated by a shaped charge under the conditions of the test.
The compositions of the invention possess the advantage that they may be slurried in an additional amount of an ammoniacal solution of ammonium nitrate and pumped into a bore hole and there allowed to settle out to form a detonable composition.
What is claimed is:
1. An ammonium nitrate explosive composition consisting essentially of particulate ammonium nitrate in admixture with from 0.5 to 20 percent by weight of finely divided carbon and with an ammoniacal solution which is substantially saturated with respect to ammonium nitrate, said ammoniacal solution containing a proportion of ammonia equivalent to from 1 to percent by weight of the total weight of the admixture, said ammoniacal solution further containing up to 30 percent by weight of water, but the said water not exceeding 3 percent of 30 percent by weight of water based on the weight of the ammoniacal solution, the said Water not exceeding 3 percent by weight of the total weight of the admixture, said ammoniacal solution having a proportion of ammonia equivalent to from about 5 to 15 percent by weight of the total weight of the admixture and said admixture containing a combined total in all phases of at least percent by weight of ammonium nitrate.
4. The explosive composition as in claim 1 admixed with from 0.12 to 5 weight percent of gum karaya whereby the viscosity of the said ammoniacal solution is increased.
References Cited in the file of this patent UNITED STATES PATENTS 2,168,562 Davis Aug. 2, 1939 2,393,594 Davis Jan. 29, 1946 2,703,528 Lee et a1. Mar. 8, 1955 2,836,484 Streng et a1. May 27, 1958 2,860,041 Griflith et a1. Nov. 11, 1958
Claims (1)
1. AN AMMONIUM NITRATE EXPLOSIVE COMPOSITION CONSISTING ESSENTIALLY OF PARTICULATE AMMONIUM NITRATE IN ADMIXTURE WITH FROM 0.5 TO 20 PERCENT BY WEIGHT OF FINELY DIVIDED CARBON AND WITH AN AMMONIACAL SOLUTION WHICH IS SUBSTANNTIALLY SATURATED WITH RESPECT TO AMMONIUM NITRATE, SAID AMMONIACAL SOLUTION CONTAINING A PROPORTION OF AMMONIA EQUIVALENT TO FROM 1 TO 30 PERCENT BY WEIGHT OF THE TOTAL WEIGHT OF THE ADMIXTURE, SAID AMMONIACAL SOLUTION FURTHER CONTAINING UP TO 30 PERCENT BY WEIGHT OF WATER, BUT THE SAID WATER NOT EXCEEDING 3 PERCENT OF THE TOTAL WEIGHT OF THE ADMIXTURE, AND SAID ADMIXTURE CONTAINING A COMBINED TOTAL IN ALL PHASES OF AT LEAST 60 PERCENT BY WEIGHT OF AMMONIUM NITRATE.
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US2992912A true US2992912A (en) | 1961-07-18 |
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US2992912D Expired - Lifetime US2992912A (en) | Ammonium nitrate explosive composition |
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3282753A (en) * | 1964-06-29 | 1966-11-01 | Intermountain Res And Engineer | Slurry blasting agent containing non-explosive liquid fuel |
US3305414A (en) * | 1963-07-25 | 1967-02-21 | Cominco Ltd | Method of comminuting ammonium nitrate prills mixed with hydrocarbon |
US3447982A (en) * | 1967-04-14 | 1969-06-03 | Commercial Solvents Corp | Ammonium nitrate having diatomaceous earth dispersed therein and method of making same |
US5480500A (en) * | 1994-10-24 | 1996-01-02 | Eti Explosives | Ammonim nitrate fuel oil blasting composition having improved water resistance |
US5925846A (en) * | 1994-10-24 | 1999-07-20 | Eti Canada | Method for the production of an ammonium nitrate fuel oil blasting composition having improved water resistance |
US6113714A (en) * | 1998-04-29 | 2000-09-05 | Eti Canada Inc. | Ammonium nitrate fuel oil blasting composition having improved water resistance |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2168562A (en) * | 1938-03-08 | 1939-08-08 | Du Pont | Inorganic nitrate explosive |
US2393594A (en) * | 1941-07-08 | 1946-01-29 | Du Pont | Operation of internal-combustion engines |
US2703528A (en) * | 1953-11-05 | 1955-03-08 | Maumee Collieries Company | Blasting process |
US2836484A (en) * | 1955-05-04 | 1958-05-27 | Reynolds Metals Co | Aqueous metal powder explosive |
US2860041A (en) * | 1955-11-17 | 1958-11-11 | Trojan Powder Co | Blasting explosives |
-
0
- US US2992912D patent/US2992912A/en not_active Expired - Lifetime
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2168562A (en) * | 1938-03-08 | 1939-08-08 | Du Pont | Inorganic nitrate explosive |
US2393594A (en) * | 1941-07-08 | 1946-01-29 | Du Pont | Operation of internal-combustion engines |
US2703528A (en) * | 1953-11-05 | 1955-03-08 | Maumee Collieries Company | Blasting process |
US2836484A (en) * | 1955-05-04 | 1958-05-27 | Reynolds Metals Co | Aqueous metal powder explosive |
US2860041A (en) * | 1955-11-17 | 1958-11-11 | Trojan Powder Co | Blasting explosives |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3305414A (en) * | 1963-07-25 | 1967-02-21 | Cominco Ltd | Method of comminuting ammonium nitrate prills mixed with hydrocarbon |
US3282753A (en) * | 1964-06-29 | 1966-11-01 | Intermountain Res And Engineer | Slurry blasting agent containing non-explosive liquid fuel |
US3447982A (en) * | 1967-04-14 | 1969-06-03 | Commercial Solvents Corp | Ammonium nitrate having diatomaceous earth dispersed therein and method of making same |
US5480500A (en) * | 1994-10-24 | 1996-01-02 | Eti Explosives | Ammonim nitrate fuel oil blasting composition having improved water resistance |
US5925846A (en) * | 1994-10-24 | 1999-07-20 | Eti Canada | Method for the production of an ammonium nitrate fuel oil blasting composition having improved water resistance |
US6113714A (en) * | 1998-04-29 | 2000-09-05 | Eti Canada Inc. | Ammonium nitrate fuel oil blasting composition having improved water resistance |
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