US3160536A - Blasting explosive - Google Patents

Blasting explosive Download PDF

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Publication number
US3160536A
US3160536A US178217A US17821762A US3160536A US 3160536 A US3160536 A US 3160536A US 178217 A US178217 A US 178217A US 17821762 A US17821762 A US 17821762A US 3160536 A US3160536 A US 3160536A
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United States
Prior art keywords
explosive
water
ammonium nitrate
hydrocarbon
mixture
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Expired - Lifetime
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US178217A
Inventor
Robert B Aitchison
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Union Carbide Corp
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Union Carbide Corp
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Publication date
Priority claimed from US708445A external-priority patent/US3064572A/en
Application filed by Union Carbide Corp filed Critical Union Carbide Corp
Priority to US178217A priority Critical patent/US3160536A/en
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Publication of US3160536A publication Critical patent/US3160536A/en
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Expired - Lifetime legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B45/00Compositions or products which are defined by structure or arrangement of component of product
    • C06B45/18Compositions or products which are defined by structure or arrangement of component of product comprising a coated component
    • C06B45/30Compositions or products which are defined by structure or arrangement of component of product comprising a coated component the component base containing an inorganic explosive or an inorganic thermic component
    • C06B45/32Compositions or products which are defined by structure or arrangement of component of product comprising a coated component the component base containing an inorganic explosive or an inorganic thermic component the coating containing an organic compound
    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B31/00Compositions containing an inorganic nitrogen-oxygen salt
    • C06B31/28Compositions containing an inorganic nitrogen-oxygen salt the salt being ammonium nitrate
    • C06B31/285Compositions containing an inorganic nitrogen-oxygen salt the salt being ammonium nitrate with fuel oil, e.g. ANFO-compositions

Definitions

  • Blast holes are commonly prepared by air drilling or wet drilling methods, and in some refractory formations of extreme hardness such as in taconite, for example, the hole is jet pierced by means of a hydrocarbon-oxygen high temperature flame. In some cases such holes have been prepared to depths greater than one hundred feet. The holes are charged with conventional cartridges of explosive which are to be detonated in the hole. Certain diificulties are often encountered when such methods are employed. Seepage water has filled such holes to substantial depths; consequently expensive high grade waterproof packed explosives have been used instead of inexpensive water sensitive compounds such as ammonium nitrate and the like. Also, blast holes may be de-watered but rain may completely ruin this work; likewise, any bags of water sensitive explosives that might be stacked near the holes ready for loading may be severely damaged from the standpoint of their use as a blasting agent.
  • An object of the invention is to provide an explosive charge including a granular water sensitive explosive.
  • a water-sensitive explosive is charged in a blast hole by placing therein "a hydrophobic explosive mixture encased within a waterimpervious flexible plastic container, the mixture comprising the water-sensitive explosive, a liquid hydrocarbon, and a hydrophobic jelling material in an amount sufficient to impart a jelly-like consistency to the liquid hydrocarbon.
  • the jelling material acts as a water-proofing agent which coats the explosive, thus rendering-the latter unaffected by accidental leakage of water into the container.
  • the water resistance of low cost, water sensitive explosives can be greatly increased by incorporating a hydrophobic jelling agent in the hydrocarbon liquid to be mixed with the granular explosive.
  • Metallic soaps have been found suitable as jelling agents.
  • kerosene was employed as the hydrocarbon liquid and to this was added an aluminum soap of Z-ethyl hexoic acid compound in the proportion of 7 /2 parts, by weight, of the soap to parts of kerosene.
  • the soap was completely dissolved in the kerosene by stirring and heating to about to F., and after cooling the liquid acquired a jelly-like consistency. Ammonium nitrate prill was then added to form a freely flowable slurry.
  • the proportions were about 1 gallon of the solution to about 80 lbs. of commercial-grade ammonium nitrate.
  • the increased Water resistance attainable by the present invention was shown experimentally by stirring ammonium nitrate with the jelly-like hydrocarbon mixture, draining off the excess liquid, and placing the otherwise unprotected aluminum nitrate in a cold water bath. It was readily apparent that the hydrophobicly jelled hydrocarbon coated the ammonium nitrate granules with a protective film, and only after 35 minutes was there any appreciable dissolving action of the water on the ammonium nitrate.
  • the hydrophobicly jelled kerosene protective film was found to be stable when immersed in water for relatively long periods, and was broken during the interim only by stirring.
  • jelled kerosene ammonium nitrate mixture is charged into the plastic bag in a bore hole, only a very small areaof the mixture adjacent a possible puncture of the intermediate tube bag can be subject to the action of water in the bore hole.
  • the dis solving action of the water is so greatly retarded that only a very small portion of the explosive can be inactivated in periods substantially longer than /2 hour,
  • hydrocarbons of the kerosene type When aluminum soaps are employed with hydrocarbons of the kerosene type, it is found that about 3% by weight of the soap is suificient to impart a jelly like consistency to the liquid with 7% the preferred upper limit, although up to about 10% by weight aluminum soap can be used.
  • suitable liquid hydrocarbons suitable for practice of the present invention include gasoline, kerosene, and fuel oil.
  • jelling agents that are hydrophobic may be used, such as colloidal carbon blacks, colloidalfsilicas, and mineral waxes.
  • the hydrocarbonjelling agent mixture should form at least about 10% by weight of the explosive.
  • the comminuted weighting material may consist of water soluble substance such as a metal salt which, when water leaks through suitably sized small punctures, will dissolve slowly to allow the explosive charge above it to sink and fill the bottom of the blast hole more snugly and completely with active explosive. In this way practically no loss in blast hole depth is sustained.
  • the metallic soap 4 being present in amount from 3% to 7% by weight of the liquid hydrocarbon, and the hydrocarbon-metallic soap mixture forming at least about 10% by weight of the mixture so as to form a jelly-like consistency which coats the ammonium nitrate.

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  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Drilling And Exploitation, And Mining Machines And Methods (AREA)

Description

United States Patent 3,160,536 BLASTING EXPLOSIVE Robert B. Aitchison, New York, N.Y., assignor to Union Carbide Corporation, a corporation of New York No Drawing. Original application Jan. 13, 1958, Ser. No. 708,445, nowPatent No. 3,064,572, dated Nov. 20, 1962. Divided and this application Jan. 30, 1962, Ser. No. 178,217 r s 1 Claim. (Cl. 149-8) The present invention relates to a water sensitive blasting explosive.
Blast holes are commonly prepared by air drilling or wet drilling methods, and in some refractory formations of extreme hardness such as in taconite, for example, the hole is jet pierced by means of a hydrocarbon-oxygen high temperature flame. In some cases such holes have been prepared to depths greater than one hundred feet. The holes are charged with conventional cartridges of explosive which are to be detonated in the hole. Certain diificulties are often encountered when such methods are employed. Seepage water has filled such holes to substantial depths; consequently expensive high grade waterproof packed explosives have been used instead of inexpensive water sensitive compounds such as ammonium nitrate and the like. Also, blast holes may be de-watered but rain may completely ruin this work; likewise, any bags of water sensitive explosives that might be stacked near the holes ready for loading may be severely damaged from the standpoint of their use as a blasting agent.
Another disadvantage of the prior art blasting methods is that the walls of the hole are quite often not perfectly regular and could cause a temporary jamming of the explosive cartridge in the hole thereby preventing their insertion to the bottom and forming an air pocket beneath and around the cartridge. It is well known that such air pockets produce a cushioning elfect which decreases the seeps into the bag and at least partially dissolves the watersensitive explosive, thereby reducing its effectiveness as an explosive.
The present application is a division of US. Patent 3,064,572issued November 20 ,1962, directed to a method and means for providing a charge of water-sensitive explosive in a blast hole. My present application is directed specificallyto a water sensitive blasting explosive for use in the method and means described in my aforementioned patent.
An object of the invention is to provide an explosive charge including a granular water sensitive explosive.
which can be placedin a water-containing blast hole without loss of brisance value. Y
In accordance with the present invention, a water-sensitive explosive is charged in a blast hole by placing therein "a hydrophobic explosive mixture encased within a waterimpervious flexible plastic container, the mixture comprising the water-sensitive explosive, a liquid hydrocarbon, and a hydrophobic jelling material in an amount sufficient to impart a jelly-like consistency to the liquid hydrocarbon. The jelling material acts as a water-proofing agent which coats the explosive, thus rendering-the latter unaffected by accidental leakage of water into the container.
- terial and fill spaces between the individual particles. Al-
It has been found that the explosive eificiency of ammonium nitrate in the form of prill can Substantially be increased by the addition of a liquid hydrocarbon. Its elfectiveness is also increased by treatment with other relatively non-compressible materials. Treatment with hydrocarbon liquid such as kerosene or fuel oils will reduce the ammonium nitrates sensitivity to Water to a certain degree but not sufliciently for present purposes.
The water resistance of low cost, water sensitive explosives can be greatly increased by incorporating a hydrophobic jelling agent in the hydrocarbon liquid to be mixed with the granular explosive. Metallic soaps have been found suitable as jelling agents. For example, in one test kerosene was employed as the hydrocarbon liquid and to this was added an aluminum soap of Z-ethyl hexoic acid compound in the proportion of 7 /2 parts, by weight, of the soap to parts of kerosene. The soap was completely dissolved in the kerosene by stirring and heating to about to F., and after cooling the liquid acquired a jelly-like consistency. Ammonium nitrate prill was then added to form a freely flowable slurry. The proportions were about 1 gallon of the solution to about 80 lbs. of commercial-grade ammonium nitrate. The increased Water resistance attainable by the present invention was shown experimentally by stirring ammonium nitrate with the jelly-like hydrocarbon mixture, draining off the excess liquid, and placing the otherwise unprotected aluminum nitrate in a cold water bath. It was readily apparent that the hydrophobicly jelled hydrocarbon coated the ammonium nitrate granules with a protective film, and only after 35 minutes was there any appreciable dissolving action of the water on the ammonium nitrate. pares favorably with a similar test in which uncoated ammonium nitrate was placed in cold water and found to dissolve immediately, and a third'test in which ammonium nitrate was coated with untreated kerosene, placed in cold water, and found to dissolve in less than 2 minutes.
Thus, the hydrophobicly jelled kerosene protective film was found to be stable when immersed in water for relatively long periods, and was broken during the interim only by stirring. When the jelled kerosene ammonium nitrate mixture is charged into the plastic bag in a bore hole, only a very small areaof the mixture adjacent a possible puncture of the intermediate tube bag can be subject to the action of water in the bore hole. The dis solving action of the water is so greatly retarded that only a very small portion of the explosive can be inactivated in periods substantially longer than /2 hour,
When aluminum soaps are employed with hydrocarbons of the kerosene type, it is found that about 3% by weight of the soap is suificient to impart a jelly like consistency to the liquid with 7% the preferred upper limit, although up to about 10% by weight aluminum soap can be used. Other suitable liquid hydrocarbons suitable for practice of the present invention include gasoline, kerosene, and fuel oil. Also, other wellsknown jelling agents that are hydrophobic may be used, such as colloidal carbon blacks, colloidalfsilicas, and mineral waxes. The hydrocarbonjelling agent mixture should form at least about 10% by weight of the explosive.
It is important that the charge fill the blast portion of the hole as" completely as possible, so as to avoid air. pockets which tend to cushion the explosion and decrease the explosive eiiiciency. To this end, it is preferable to employ a weighting material having a high bulk density and which is comminuted fine enough to spread out against the bottom of the blasthole so as to avoid air spaces. Since water in the blast hole contributes to fill any spaces as anon-compressible shock transmitting medium, it will be advantageous to-puncture the weight material bag so I that water can mix with the comminuted weightingma- This com- I 3 ternatively, it is also contemplated that the comminuted weighting material may consist of water soluble substance such as a metal salt which, when water leaks through suitably sized small punctures, will dissolve slowly to allow the explosive charge above it to sink and fill the bottom of the blast hole more snugly and completely with active explosive. In this way practically no loss in blast hole depth is sustained.
What is claimed is:
An explosive mixture for charging blast holes which 10 2,211,738
comprises a mixture of granular ammonium nitrate, a liquid hydrocarbon and a metallic soap, the metallic soap 4 being present in amount from 3% to 7% by weight of the liquid hydrocarbon, and the hydrocarbon-metallic soap mixture forming at least about 10% by weight of the mixture so as to form a jelly-like consistency which coats the ammonium nitrate.
References Cited in the tile of this patent UNITED STATES PATENTS 474,529 Roller May 10, 1892 Cairns Aug. 13, 1940 2,398,071 Barab Apr. 9, 1946 2,630,379 Lytle Mar. 3, 1953
US178217A 1958-01-13 1962-01-30 Blasting explosive Expired - Lifetime US3160536A (en)

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Application Number Priority Date Filing Date Title
US178217A US3160536A (en) 1958-01-13 1962-01-30 Blasting explosive

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US708445A US3064572A (en) 1958-01-13 1958-01-13 Method of and means for providing a charge of water sensitive explosive in a blast hole
US178217A US3160536A (en) 1958-01-13 1962-01-30 Blasting explosive

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Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3287189A (en) * 1964-03-02 1966-11-22 Dow Chemical Co Coated explosive comprising ammonium nitrate
US4736683A (en) * 1986-08-05 1988-04-12 Exxon Chemical Patents Inc. Dry ammonium nitrate blasting agents
US5480500A (en) * 1994-10-24 1996-01-02 Eti Explosives Ammonim nitrate fuel oil blasting composition having improved water resistance
US5486246A (en) * 1994-09-15 1996-01-23 Arcadian Fertilizer, L.P. High density ammonium nitrate prill and method of production of the same
US5527498A (en) * 1994-09-15 1996-06-18 Arcadian Fertilizer, L.P. Method for production of high density ammonium nitrate prills
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
US20050269002A1 (en) * 2004-04-08 2005-12-08 Nexco Inc. Ammonium nitrate blasting agent and method of production
US20060219338A1 (en) * 2004-04-07 2006-10-05 Nexco Inc. Ammonium nitrate crystals, ammonium nitrate blasting agent and method of production
EP2780302A4 (en) * 2011-11-17 2015-07-22 Dyno Nobel Asia Pacific Pty Ltd Blasting compositions

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US474529A (en) * 1892-05-10 Manufacture of explosives
US2211738A (en) * 1937-07-08 1940-08-13 Hercules Powder Co Ltd Blasting explosive
US2398071A (en) * 1940-07-24 1946-04-09 Barab Jacob Ammonium nitrate explosives
US2630379A (en) * 1949-10-14 1953-03-03 Atlas Powder Co Method of improving the waterresistance of ammonium nitrate explosives

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US474529A (en) * 1892-05-10 Manufacture of explosives
US2211738A (en) * 1937-07-08 1940-08-13 Hercules Powder Co Ltd Blasting explosive
US2398071A (en) * 1940-07-24 1946-04-09 Barab Jacob Ammonium nitrate explosives
US2630379A (en) * 1949-10-14 1953-03-03 Atlas Powder Co Method of improving the waterresistance of ammonium nitrate explosives

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3287189A (en) * 1964-03-02 1966-11-22 Dow Chemical Co Coated explosive comprising ammonium nitrate
US4736683A (en) * 1986-08-05 1988-04-12 Exxon Chemical Patents Inc. Dry ammonium nitrate blasting agents
US5486246A (en) * 1994-09-15 1996-01-23 Arcadian Fertilizer, L.P. High density ammonium nitrate prill and method of production of the same
US5527498A (en) * 1994-09-15 1996-06-18 Arcadian Fertilizer, L.P. Method for production of high density ammonium nitrate prills
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
US20060219338A1 (en) * 2004-04-07 2006-10-05 Nexco Inc. Ammonium nitrate crystals, ammonium nitrate blasting agent and method of production
US7767045B2 (en) 2004-04-07 2010-08-03 Nexco Inc. Ammonium nitrate crystals, ammonium nitrate blasting agent and method of production
US20100258222A1 (en) * 2004-04-07 2010-10-14 Nexco Inc. Ammonium nitrate crystals, ammonium nitrate blasting agent and method of production
US20050269002A1 (en) * 2004-04-08 2005-12-08 Nexco Inc. Ammonium nitrate blasting agent and method of production
EP2780302A4 (en) * 2011-11-17 2015-07-22 Dyno Nobel Asia Pacific Pty Ltd Blasting compositions
US10723670B2 (en) 2011-11-17 2020-07-28 Dyno Nobel Asia Pacific Pty Limited Blasting compositions

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