US3160536A - Blasting explosive - Google Patents
Blasting explosive Download PDFInfo
- 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
- Authority
- US
- United States
- Prior art keywords
- explosive
- water
- ammonium nitrate
- hydrocarbon
- mixture
- 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
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B45/00—Compositions or products which are defined by structure or arrangement of component of product
- C06B45/18—Compositions or products which are defined by structure or arrangement of component of product comprising a coated component
- C06B45/30—Compositions 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
- C06B45/32—Compositions 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
-
- 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
- C06B31/285—Compositions 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
Priority Applications (1)
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 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3160536A true US3160536A (en) | 1964-12-08 |
Family
ID=26874106
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US178217A Expired - Lifetime US3160536A (en) | 1958-01-13 | 1962-01-30 | Blasting explosive |
Country Status (1)
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US (1) | US3160536A (en) |
Cited By (10)
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)
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 |
-
1962
- 1962-01-30 US US178217A patent/US3160536A/en not_active Expired - Lifetime
Patent Citations (4)
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)
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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