US2967099A - Foamed liquid explosive composition - Google Patents

Foamed liquid explosive composition Download PDF

Info

Publication number
US2967099A
US2967099A US667996A US66799657A US2967099A US 2967099 A US2967099 A US 2967099A US 667996 A US667996 A US 667996A US 66799657 A US66799657 A US 66799657A US 2967099 A US2967099 A US 2967099A
Authority
US
United States
Prior art keywords
explosive
foam
liquid
stearate
blanket
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
US667996A
Inventor
John E Pool
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
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.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to US667996A priority Critical patent/US2967099A/en
Application granted granted Critical
Publication of US2967099A publication Critical patent/US2967099A/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
    • C06B23/002Sensitisers or density reducing agents, foam stabilisers, crystal habit modifiers
    • 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
    • C06B23/002Sensitisers or density reducing agents, foam stabilisers, crystal habit modifiers
    • C06B23/004Chemical sensitisers
    • 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
    • C06B23/007Ballistic modifiers, burning rate catalysts, burning rate depressing agents, e.g. for gas generating
    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B25/00Compositions containing a nitrated organic compound
    • C06B25/36Compositions containing a nitrated organic compound the compound being a nitroparaffin

Definitions

  • This invention relates to new compositions adapted for use in a novel method of actuating land mines buried beneath the surface of the ground. More particularly the invention concerns foam producing compositions capable of being formed into a blanket of explosive foam over designated areas of terrain, as for example enemy mine fields and the like, and which may be detonated by conventional means.
  • the prior art methods of clearing mine fields may be placed in two broad classes, namely; physical removal of the mines, and actuation of the mines.
  • the latter class may be further divided into two categories; actuation by mechanical means such as the flail, and actuation of the mines by an explosive blast.
  • One example of the latter category is'" the use of the mine clearing snake disclosed in U.S. Patent No. 2,511,005. It is known that blast resistant mine fuzes can be actuated by less than 4 lb. of explosive per square foot of area if the mine is directly beneath the explosive charge. Therefore, if a mine field could be blanketed with a layer of explosive material amounting to about lb. per square foot, upon detonation, all the mines within the blanketed area would be effectively actuated.
  • a primary object of this invention is the development of an efiici'ent, easily operated method of actuating land mines planted over a relatively large area of terrain.
  • 'A further object of this invention is the development of a fluid explosive composition suitable for distribution over all types of terrain in the form of a blanket capable of being detonated by conventional means and which is sufliciently uniform to propagate the detonation throughout the blanket mass.
  • a still further object of the invention is the provision of a low density explosive capable of being projected over enemy minefields as a blanket and which on detonation will actuate and destroy mines buried in the ground beneath the explosive blanket.
  • liquid explosive compositions may be Whipped into explosive foams of considerably increased volume.
  • the resulting foams may readily be distributed over wide areas of terrain of all types, thus obviating all or most of the difiiculties previously encountered in the use of liquid explosives in clearing mine fields.
  • Such an explosive foam is particularly advantageous since the presence. of finely divided, uniformly distributed explosive particles in the foam act to ensure complete initiation, detonation and propagation throughout the mass of foam.
  • the physical consistency of the foam ensures continuous coverage over uneven ground, grass, small shrubs, wire etc. and will prevent excessive loss of explosive material through absorption into the ground.
  • the low density of such foamed explosives permit coverage adequate to produce the required blast effect without using an excessive weight of explosive per square foot of area.
  • liquid explosive which will be stable during transportation and which may be sensitized by means of a sensitizing agent such as ethylene diamine after arrival at the area of operations.
  • the liquid explosive must further be suitable for whipping into a relatively stable foam by conventional means.
  • the cohmive and flow properties of the foam must be such that it is projectable and will satisfactorily spread over the ground in a uniform blanket; there must be suflicient expansion in volume over the initial liquid to provide economy in the use of the explosive; the foam must be suificiently stable under various prospective conditions of combat (normal weather, hot air, rain, sandy ground, turf, etc.) to make its use practicable, and finally the foam must be detonatable at a thickness which provides a sufliciently large coverage per tank of initial liquid and still provide force sufiicient to actuate all mines lying beneath the blanket.
  • the explosive foam composition of this invention comprises a mixture of a suitable liquid explosive material; a foaming agent in a finely divided state, a sensitizer and where applicable a foam stabilizing agent.
  • a suitable liquid explosive material e.g., a gas, a gas, or a gas.
  • Any liquid explosive capable of being foamed may be employed for the purposes of this invention.
  • explosives such as nitromethane or nitropropaneare to be preferred since they may be safely transported to the field of operations where a sensitizer may be incorporated at the time of foaming.
  • Mechanical foams are generally produced by mixing a foaming agent with a liquid medium, in this .case the liquid explosive, and then adding a stabilizing agent which acts to prolong the life of the foam.
  • the foaming and stabilizing agents may, and the same material so that only one material need be added. A satisfactory foam cannot be produced, however, with much less than 10% of solids present.
  • sensitizing agents which may be employed are ethylene diamine and morpholine (diethylenimide oxide) or a solution of these amines in an alcohol such as methanol, propanol or butanol.
  • Surface active agents found to be suitable for use as foaming agents in forming stable foams, with or without the additional use of stabilizers include zinc stearate, lithium stearate, magnesium stearate, sodium stearate, Acr-awax C (an octadecenamide), polyethylene glycol 42, Carbowax 1000 monostearate and Carbowax 4000 monostearate (the monostearates of polyethylene glycols having molecular weights of 1000 and 4000 respectively), and polyethylene glycol 400 mono stearate, either alone or in conjunction with stearic acid in a 1:1 weight ratio.
  • the above explosive compositions are intended to be handled as two component mixtures. In practice from 5% to 15% of the sensitizing solution is mixed with the main composition just prior to use. By following this procedure the solutions can be handled as insensitive, inflammable but non-explosive materials.
  • the gas-retaining capacity of the liquid explosive composition is an important factor in increasing the foam volume of systems such as given in Table 1.
  • the gas retaining capacity of nitromethane may be noticeably increased by the addition of methanol, isopropanol or dibutyl tin diacetate.
  • isopropyl alcohol in conjunction with the solid stabilizer 36% of total inert material.
  • Example 23 liquid mixture was mixed with a perforated wooden paddle 7, Percent for four minutes, after which the volume increase was Nitromethane 87.4 noted.
  • the drainage was measured by pouring the foam Magnesium stearate 76 onto a 325 mesh screen 5 inches in diameter and 1 /2 75 Ethylene diamine 5.0
  • Example 25 Nitromethane 78.2 Nitropropane 13.8 Magnesium stearate 7.9 Silicon dioxide 0.1
  • foamable explosive compositions were found suitable for use in accomplishing the objects of this invention. All of these compositions exhibited an increase of at least 100% in volume on being foamed. Each of the foamed compositions could be projected and formed into a continuous relatively uniform blanket effectively covering any designated area of terrain and which could be detonated regularly when the blanket was as thin as 4 inch.
  • suitable identification means may be incorporated in the foamed explosive for the purpose of defining the area of terrain cleared of mines, particularly where such area is in the form of a tortuous path. Also, the presence of identification means would act to alert troops arriving at the area of operations at a later hour, of the fact that said area had been cleared.
  • any dye particularly of the fluorescent type, light reflecting particles of the type used on highway signs, or any other coloring, light emitting or light reflecting material which would not be destroyed by the detonation may be incorporated in the foamed explosive.
  • a sensitizing agent selected from the group consisting of ethylene diamine and morpholine.
  • composition according to claim 1 wherein said composition contains a stabilizing agent selected from the group consisting of methanol, ethanol, isopropanol, isobutanol, dibutyl tin diacetate and silicon dioxide.
  • a stabilizing agent selected from the group consisting of methanol, ethanol, isopropanol, isobutanol, dibutyl tin diacetate and silicon dioxide.
  • composition according to claim 3 wherein the sensitizing agent is in solution in a lower aliphatic alcohol.
  • a foamable liquid explosive composition consisting essentially of a liquid nitroparaflin selected from the group consisting of nitromethane, nitropropane and mixture thereof, of from about 7.6 to 10 percent by weight of a metal stearate selected from the group consisting of magnesium, lithium, zinc and sodium stearates, and of from about 5 to 15 percent by weight of a sensitizing agent selected from the group consisting of ethylene diamine and morpholine.
  • a composition according to claim 4 which contains a stabilizing agent selected from the group consisting of lower aliphatic alcohols, dibutyl tin acetate and silicon dioxide.
  • composition according to claim 4 wherein the metal stearate is lithium stearate.
  • composition according to claim 5 wherein the stabilizing agent is isopropyl alcohol.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Description

" a gelatiniz-ing agent be employed mamas Patented Jan. 3, 1961 2,967,099 FOAMED LIQUID EXPLOSIVE COMPOSITION John E. Pool, 312 W. Hunting Towers Apt, Alexandria, Va.
No Drawing. Filed June 25, 1957, Ser. No. 667,996 '7 Claims. (Cl. 52-5) (Granted under Title 35,-U.S. Code (1952), sec. 266) The invention described herein may be manufactured and used by or for the Government for governmental purposes, without the payment to me of any royalty thereon.
This invention relates to new compositions adapted for use in a novel method of actuating land mines buried beneath the surface of the ground. More particularly the invention concerns foam producing compositions capable of being formed into a blanket of explosive foam over designated areas of terrain, as for example enemy mine fields and the like, and which may be detonated by conventional means.
In general, the prior art methods of clearing mine fields may be placed in two broad classes, namely; physical removal of the mines, and actuation of the mines. The latter class may be further divided into two categories; actuation by mechanical means such as the flail, and actuation of the mines by an explosive blast. One example of the latter category is'" the use of the mine clearing snake disclosed in U.S. Patent No. 2,511,005. It is known that blast resistant mine fuzes can be actuated by less than 4 lb. of explosive per square foot of area if the mine is directly beneath the explosive charge. Therefore, if a mine field could be blanketed with a layer of explosive material amounting to about lb. per square foot, upon detonation, all the mines within the blanketed area would be effectively actuated.
The desirability of liquid explosives for mine field clearance has been recognized. However, serious difiiculties have been encountered in their use by reason of their tendency to be rapidly absorbed into the ground, thus making detonation impossible. Furthermore, attempts to spread liquid explosives over irregular ground surfaces resulted in the formation of puddles and bare spots. Obviously this type of a discontinuous explosive surface layer cannot be reliably detonated by conventional methods of initiation.
To obviate the latter difiiculties, it was suggested that to form a relatively non-absorbable ground blanket. Although the use of thixotropic gelatinized liquid explosives were more successful in preventing the absorption of the explosive into the soil, the method proved unsatisfactory in that it was diflicult to lay the continuous, relatively uniform blanket necessary to achieve complete detonation and activation of all the mines planted within the blanketed area. Furthermore, cracking and fissuring of the ground blanket occurred to such an extent that the material could not be completely detonated, and reliable detonation and propagation could not be achieved unless the gelled explosive layer was much thicker than was needed to produce the explosive force required to actuate the mines.
Accordingly, a primary object of this invention is the development of an efiici'ent, easily operated method of actuating land mines planted over a relatively large area of terrain.
'A further object of this invention is the development of a fluid explosive composition suitable for distribution over all types of terrain in the form of a blanket capable of being detonated by conventional means and which is sufliciently uniform to propagate the detonation throughout the blanket mass.
A still further object of the invention is the provision of a low density explosive capable of being projected over enemy minefields as a blanket and which on detonation will actuate and destroy mines buried in the ground beneath the explosive blanket.
Accordingly, pursuant to the above objects, I have now discovered that by the use of suitable foaming and stabilizing agents, liquid explosive compositions may be Whipped into explosive foams of considerably increased volume. The resulting foams may readily be distributed over wide areas of terrain of all types, thus obviating all or most of the difiiculties previously encountered in the use of liquid explosives in clearing mine fields. Such an explosive foam is particularly advantageous since the presence. of finely divided, uniformly distributed explosive particles in the foam act to ensure complete initiation, detonation and propagation throughout the mass of foam. The physical consistency of the foam ensures continuous coverage over uneven ground, grass, small shrubs, wire etc. and will prevent excessive loss of explosive material through absorption into the ground. Furthermore, the low density of such foamed explosives permit coverage adequate to produce the required blast effect without using an excessive weight of explosive per square foot of area.
For the purpose of this invention it is desirable to use a liquid explosive which will be stable during transportation and which may be sensitized by means of a sensitizing agent such as ethylene diamine after arrival at the area of operations. The liquid explosive must further be suitable for whipping into a relatively stable foam by conventional means. In order to be ideally suited for the intended use the cohmive and flow properties of the foam must be such that it is projectable and will satisfactorily spread over the ground in a uniform blanket; there must be suflicient expansion in volume over the initial liquid to provide economy in the use of the explosive; the foam must be suificiently stable under various prospective conditions of combat (normal weather, hot air, rain, sandy ground, turf, etc.) to make its use practicable, and finally the foam must be detonatable at a thickness which provides a sufliciently large coverage per tank of initial liquid and still provide force sufiicient to actuate all mines lying beneath the blanket.
Briefly, the explosive foam composition of this invention comprises a mixture of a suitable liquid explosive material; a foaming agent in a finely divided state, a sensitizer and where applicable a foam stabilizing agent. Such compositions when mechanically whipped will form a foam of low density which will detonate when initiated by a conventional blasting cap when spread in the form of a blanket as thin as 4 inch.
Any liquid explosive capable of being foamed may be employed for the purposes of this invention. However, explosives such as nitromethane or nitropropaneare to be preferred since they may be safely transported to the field of operations where a sensitizer may be incorporated at the time of foaming.
Mechanical foams'are generally produced by mixing a foaming agent with a liquid medium, in this .case the liquid explosive, and then adding a stabilizing agent which acts to prolong the life of the foam. The foaming and stabilizing agents may, and the same material so that only one material need be added. A satisfactory foam cannot be produced, however, with much less than 10% of solids present. The
' additives necessary to obtain foaming and stabilization in some instances, be one.
should, of course, not noticeably desensitize the liquid explosive material.
Among the sensitizing agents which may be employed are ethylene diamine and morpholine (diethylenimide oxide) or a solution of these amines in an alcohol such as methanol, propanol or butanol.
Surface active agents found to be suitable for use as foaming agents in forming stable foams, with or without the additional use of stabilizers include zinc stearate, lithium stearate, magnesium stearate, sodium stearate, Acr-awax C (an octadecenamide), polyethylene glycol 42, Carbowax 1000 monostearate and Carbowax 4000 monostearate (the monostearates of polyethylene glycols having molecular weights of 1000 and 4000 respectively), and polyethylene glycol 400 mono stearate, either alone or in conjunction with stearic acid in a 1:1 weight ratio.
The invention can best be understood from the following specific examples, which, however, are not to be taken as limiting the scope of the invention but are cited Example 20 Nitromethane cc 210 Isopropanol cc 90 Ethylene diamine cc Lithium stearate grams 30 When foamed, the above mixture had a volume of 640 as being amang the preferred embodiments themofi cc. The drainage from the foamed mass was as follovs: 0. TABLE NO. 1 min- 6 in. 10 Example No. 20 Composition (parts by wt.) 3 min. 30
min. 1 2 3 4 5 6 4 min. 42 Nltromethane 92 9o 9o 5 52 Nltromethane-nitropropane 92 90 90 E l 21 Magnesium stearate 8 8 Lithium stearate 10 10 Nltromethane 0..- 210 Zinc stearate 10 lsopropanol 90 Sensitizer:
Ethlylene giammeu n n n x x x Lithium stearate grams 30 Et len amineco 0 2 x x y e a X ThlS formulatlon contains approxrmately 9% sohds and 1 85 parts nitromethane15 parts nitropropane.
= 3 parts ethylene diamine-1 part ethyl, methyl or propyl alcohol.
The above explosive compositions are intended to be handled as two component mixtures. In practice from 5% to 15% of the sensitizing solution is mixed with the main composition just prior to use. By following this procedure the solutions can be handled as insensitive, inflammable but non-explosive materials.
The gas-retaining capacity of the liquid explosive composition is an important factor in increasing the foam volume of systems such as given in Table 1. As the result of a study of the effect of the addition of various solvents to the nitromethane composition, it was found that the gas retaining capacity of nitromethane may be noticeably increased by the addition of methanol, isopropanol or dibutyl tin diacetate. Of particular interest was the use of isopropyl alcohol in conjunction with the solid stabilizer 36% of total inert material. When mechanically stirred at 1400 rpm. for two minutes the composition had a foamed volume of 620 cc. The volume of liquid drained from the foamed mass was as follows:
Time (seconds) Volume (cc.)
Example 22 Time (seconds) Volume (cc.)
hthium stearate. 30
The eifect on foam volume and stability of variations in 7 the amount and type of stabilizing, foaming and sensitizing 12 agents is shown in the following table: 17
TABLE NO. 2
Nitro- Anhydrous Lithium Foam Volume Example No. methane, Isopropanol, cc. Ethylene stearate, Volume, Drainage Percent cc. Diamine, gm. cc. 2 Min., Drainage 300 so 22. 5 e00 4a. 5
300 3o 30 650 as 28.2
240 so 30 690 so 24.2
210 90 (Isobutano 30 so 700 so 24.2
210 so (Ethanol)-. 30 30 670 90 27.3
In each of the compositions shown in Table No. 2, the Example 23 liquid mixture was mixed with a perforated wooden paddle 7, Percent for four minutes, after which the volume increase was Nitromethane 87.4 noted. The drainage was measured by pouring the foam Magnesium stearate 76 onto a 325 mesh screen 5 inches in diameter and 1 /2 75 Ethylene diamine 5.0
Example 24 Nitromethane 74.3 Nitropropane 13.1 Magnesium stearate 7.6 Ethylene diamine 3.75 Ethyl alcohol 1.25
Example 25 Nitromethane 78.2 Nitropropane 13.8 Magnesium stearate 7.9 Silicon dioxide 0.1
Each of the above examples of foamable explosive compositions were found suitable for use in accomplishing the objects of this invention. All of these compositions exhibited an increase of at least 100% in volume on being foamed. Each of the foamed compositions could be projected and formed into a continuous relatively uniform blanket effectively covering any designated area of terrain and which could be detonated regularly when the blanket was as thin as 4 inch.
Detonation tests were performed on porous sand so that any liquid which drained away from the foam would be removed and could not aid in transmitting the detonation. In forming the explosive blanket the foam was projected through a nozzle which has two venturi tubes, one of which meters the solution containing the foaming and stabilizing agents while the other meters the amount of air which is introduced into the mixture.
Where desired suitable identification means may be incorporated in the foamed explosive for the purpose of defining the area of terrain cleared of mines, particularly where such area is in the form of a tortuous path. Also, the presence of identification means would act to alert troops arriving at the area of operations at a later hour, of the fact that said area had been cleared. For this purpose any dye, particularly of the fluorescent type, light reflecting particles of the type used on highway signs, or any other coloring, light emitting or light reflecting material which would not be destroyed by the detonation may be incorporated in the foamed explosive.
While the instant invention has been shown and described herein in what are conceived to be the most practical and preferred embodiments, it is to be recognized that departures may be made therefrom within the scope of the invention, which is therefore not to be limited to the details disclosed herein but is to be accorded the full about 7.6 to percent by weight of a metal stearate selected from the group consisting of magnesium, lithium,
zinc and sodium stearates, and of from about 5 to 15 percent by weight of a sensitizing agent selected from the group consisting of ethylene diamine and morpholine.
2. The composition according to claim 1 wherein said composition contains a stabilizing agent selected from the group consisting of methanol, ethanol, isopropanol, isobutanol, dibutyl tin diacetate and silicon dioxide.
3. The composition according to claim 1 wherein the sensitizing agent is in solution in a lower aliphatic alcohol.
4. A foamable liquid explosive composition consisting essentially of a liquid nitroparaflin selected from the group consisting of nitromethane, nitropropane and mixture thereof, of from about 7.6 to 10 percent by weight of a metal stearate selected from the group consisting of magnesium, lithium, zinc and sodium stearates, and of from about 5 to 15 percent by weight of a sensitizing agent selected from the group consisting of ethylene diamine and morpholine.
5. A composition according to claim 4 which contains a stabilizing agent selected from the group consisting of lower aliphatic alcohols, dibutyl tin acetate and silicon dioxide.
6. The composition according to claim 4 wherein the metal stearate is lithium stearate.
7. The composition according to claim 5 wherein the stabilizing agent is isopropyl alcohol.
References Cited in the file of this patent UNITED STATES PATENTS 2,504,119 Frazer Apr. 18,1950
2,685,251 Davis et al. Aug. 3, 1954 2,692,195 Hannum et al. Oct. 19, 1954 2,721,792 Hannum Oct. 25, 1955 FOREIGN PATENTS 17,891 Great Britain 1906 490,744 Canada Feb. 24, 1953

Claims (1)

1. A FOAMABLE LIQUID EXPLOSIVE COMPOSITION CONSISTING ESSENTIALLY OF A LIQUID NITROPARAFFIN HYDROCARBON, OF FROM ABOUT 7.6 TO 10 PERCENT BY WEIGHT OF A METAL STEARATE SELECTED FROM THE GROUP CONSISTING OF MAGNESIUM, LITHIUM, ZINC AND SODIUM STEARATES, AND OF FROM ABOUT 5 TO 15 PERCENT BY WEIGHT OF A SENSITIZING AGENT SELECTED FROM THE GROUP CONSISTING OF ETHYLENE DIAMINE AND MORPHOLINE.
US667996A 1957-06-25 1957-06-25 Foamed liquid explosive composition Expired - Lifetime US2967099A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US667996A US2967099A (en) 1957-06-25 1957-06-25 Foamed liquid explosive composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US667996A US2967099A (en) 1957-06-25 1957-06-25 Foamed liquid explosive composition

Publications (1)

Publication Number Publication Date
US2967099A true US2967099A (en) 1961-01-03

Family

ID=24680551

Family Applications (1)

Application Number Title Priority Date Filing Date
US667996A Expired - Lifetime US2967099A (en) 1957-06-25 1957-06-25 Foamed liquid explosive composition

Country Status (1)

Country Link
US (1) US2967099A (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1167238B (en) * 1961-05-16 1964-04-02 Aerojet General Co Sensitized nitro paraffin explosives
DE1215306B (en) * 1963-02-27 1966-04-28 Rheinische Maschinenfabrik & E Foundry core manufacturing machine
US3309251A (en) * 1966-08-12 1967-03-14 Ludwig F Audrieth Liquid explosive mixture containing nitromethane and ethylenediamine
US3638569A (en) * 1968-08-01 1972-02-01 Messerschmitt Boelkow Blohm Method and equipment for the elimination of mine blockades
US3713915A (en) * 1970-11-23 1973-01-30 Amoco Prod Co Thickened nitromethane explosive containing encapsulated sensitizer
US3798092A (en) * 1972-08-25 1974-03-19 Commerical Solvents Corp Low-temperature liquid explosive composition
US3904452A (en) * 1972-06-29 1975-09-09 Nitro Nobel Ab Method for the stabilization of aqueous solutions of nitroform and stabilized such solutions
US4925505A (en) * 1988-08-10 1990-05-15 Her Majesty The Queen In Right Of Canada As Represented By The Minister Of National Defence Foamed nitroparaffin explosive composition
US5047098A (en) * 1983-03-04 1991-09-10 Rheinmetall Gmbh Liquid propellant
US20180036566A1 (en) * 2015-02-13 2018-02-08 Tyco Fire Products Lp Use of an indicator as a marker in foam concentrates

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB190617891A (en) * 1905-10-21 1906-10-18 Westf Anhaltische Sprengstoff Improvements relating to Nitro-glycerine-explosives.
US2504119A (en) * 1945-06-20 1950-04-18 Joseph H Frazer Producing explosions on surfaces
CA490744A (en) * 1953-02-24 A. Laurence Edgar Nitromethane explosive containing amines
US2685251A (en) * 1947-12-17 1954-08-03 Du Pont Method of blasting
US2692195A (en) * 1947-09-04 1954-10-19 Borg Warner Nitroparaffin fuel
US2721792A (en) * 1946-05-07 1955-10-25 Borg Warner Nitro-paraffin propellant

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA490744A (en) * 1953-02-24 A. Laurence Edgar Nitromethane explosive containing amines
GB190617891A (en) * 1905-10-21 1906-10-18 Westf Anhaltische Sprengstoff Improvements relating to Nitro-glycerine-explosives.
US2504119A (en) * 1945-06-20 1950-04-18 Joseph H Frazer Producing explosions on surfaces
US2721792A (en) * 1946-05-07 1955-10-25 Borg Warner Nitro-paraffin propellant
US2692195A (en) * 1947-09-04 1954-10-19 Borg Warner Nitroparaffin fuel
US2685251A (en) * 1947-12-17 1954-08-03 Du Pont Method of blasting

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1167238B (en) * 1961-05-16 1964-04-02 Aerojet General Co Sensitized nitro paraffin explosives
DE1215306B (en) * 1963-02-27 1966-04-28 Rheinische Maschinenfabrik & E Foundry core manufacturing machine
US3309251A (en) * 1966-08-12 1967-03-14 Ludwig F Audrieth Liquid explosive mixture containing nitromethane and ethylenediamine
US3638569A (en) * 1968-08-01 1972-02-01 Messerschmitt Boelkow Blohm Method and equipment for the elimination of mine blockades
US3713915A (en) * 1970-11-23 1973-01-30 Amoco Prod Co Thickened nitromethane explosive containing encapsulated sensitizer
US3904452A (en) * 1972-06-29 1975-09-09 Nitro Nobel Ab Method for the stabilization of aqueous solutions of nitroform and stabilized such solutions
US3798092A (en) * 1972-08-25 1974-03-19 Commerical Solvents Corp Low-temperature liquid explosive composition
US5047098A (en) * 1983-03-04 1991-09-10 Rheinmetall Gmbh Liquid propellant
US4925505A (en) * 1988-08-10 1990-05-15 Her Majesty The Queen In Right Of Canada As Represented By The Minister Of National Defence Foamed nitroparaffin explosive composition
GB2243827A (en) * 1988-08-10 1991-11-13 Canada Minister Defence Foamable explosive compositions
GB2243827B (en) * 1988-08-10 1994-05-11 Canada Minister Defence Foamable explosive compositions
US20180036566A1 (en) * 2015-02-13 2018-02-08 Tyco Fire Products Lp Use of an indicator as a marker in foam concentrates
US10786696B2 (en) * 2015-02-13 2020-09-29 Tyco Fire Products Lp Use of an indicator as a marker in foam concentrates

Similar Documents

Publication Publication Date Title
US2967099A (en) Foamed liquid explosive composition
JPS6140893A (en) Water in oil emulsion explosive
US2925038A (en) Method of clearing mine fields
US4414044A (en) Water-in-oil emulsion explosive composition
US3419444A (en) Thickened aqueous inorganic nitrate salt-nitroparaffin explosive composition sensitized with an air entrapping material
US3212944A (en) Ammonium nitrate compositions containing hydratable metal salts and methods for producing the same
US4600452A (en) Eutectic microknit composite explosives and processes for making same
US5472529A (en) Explosive composition and method for producing the same
US6293201B1 (en) Chemically reactive fragmentation warhead
US2704515A (en) Method of loading for liquid oxygen explosives
US3596602A (en) Distributed explosives agent dispersal system
US3985593A (en) Water gel explosives
US4908080A (en) Water-in-oil type emulsion explosive with chelating agent
US4925505A (en) Foamed nitroparaffin explosive composition
CA1063356A (en) Nitroparaffin explosive composition
US3240641A (en) Ammonium nitrate-hydrocarbon oil explosive composition
US4042431A (en) Two component field mix hydrazine base explosive
US2504119A (en) Producing explosions on surfaces
US4219374A (en) Monopropellant composition
US3266960A (en) Ammonium nitrate compositions containing hydratable metal salts and liquid hydrocarbons
US3085047A (en) Stabilization of diphenylaminechlorarsine gas generating charges by coating the particles with a drying oil
US3155554A (en) Liquid blanketed chlorate blasting agent
US1948583A (en) Method of and explosive for blasting deep well holes
Wright Ionosonde studies of some chemical releases in the ionosphere
US2667122A (en) Oil well torpedo