US3711345A - Chemical foaming of water-bearing explosives - Google Patents

Chemical foaming of water-bearing explosives Download PDF

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US3711345A
US3711345A US00064793A US3711345DA US3711345A US 3711345 A US3711345 A US 3711345A US 00064793 A US00064793 A US 00064793A US 3711345D A US3711345D A US 3711345DA US 3711345 A US3711345 A US 3711345A
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blasting
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gas
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E Tomic
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ETI EXPLOSIVES TECHNOLOGIES INTE
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EI Du Pont de Nemours and Co
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    • C—CHEMISTRY; METALLURGY
    • C06—EXPLOSIVES; MATCHES
    • C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B47/00—Compositions in which the components are separately stored until the moment of burning or explosion, e.g. "Sprengel"-type explosives; Suspensions of solid component in a normally non-explosive liquid phase, including a thickened aqueous phase
    • C06B47/14—Compositions in which the components are separately stored until the moment of burning or explosion, e.g. "Sprengel"-type explosives; Suspensions of solid component in a normally non-explosive liquid phase, including a thickened aqueous phase comprising a solid component and an aqueous phase

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  • Water-bearing blasting agents are well known. These products typically comprise an oxidizing component, usually predominantly ammonium nitrate, a fuel component and water. More particularly, these blasting agents are referred to in the art as water-gels or slurry explosives, and emulsion type blasting agents.
  • the blasting agents commonly referred to as water gels contain, in addition to the above ingredients, a thickening agent that gels the composition, e.g., guar gum or polyacrylamides.
  • the water gels may contain high explosives such as TNT or metallic fuels such as aluminum that function not only as part of the fuel component of the blasting agent but also increase explosive strength.
  • Emulsion type blasting agents contain at least one oxidizing agent, water, an emulsifying agent, and a fuel component that is a carbonaceous compound insoluble in water.
  • the carbonaceous fuel used in the process for preparing these products is liquid during formation of the emulsion.
  • the emulsifying agent generally forms a water-in-oil emulsion wherein oil is the continuous phase and water is the discontinuous phase of the emulsion.
  • Representative water-bearing semisolid colloidal dispersions of emulsion type blasting agents are described in US. Pat. 3,447,978. Furthermore, these semisolid colloidal dispersions of water-bearing blasting agents, both the thickened water gel and emulsion type, have been prepared in such a manner that small gas bubbles are entrapped therein or they contain gas-entrapping material, e.g., microballoons. The inclusion of gas in the form of bubbles or in gas-entrapping material is known to regulate the strength of the blasting agent.
  • Methods for preparing gas-containing water-bearing blasting agents include the mechanical incorporation of gas and in situ chemical generation of gas by the decomposition of certain compounds.
  • This invention provides a process for preparing foamed semisolid colloidal dispersions of Water-bearing blasting agents, especially water gels 0r thickened water-bearing explosives, and emulsion type blasting agents, which comprises mixing inorganic oxidizing salt, fuel and water, the improvement which comprises incorporating into the mix an alkali metal borohydride gas-generating material thereby foaming and sensitizing the blasting agent.
  • a thickening agent e.g., guar gum
  • an emulsifying agent and a liquid carbonaceous fuel are added to the water-bearing explosive during preparation in order to form an emulsion between the water and fuel.
  • the amount of alkali metal borohydride added to the mix is about from 0.002 to 0.10% based on the weight of the total composition.
  • the gas-generating materials that are used in the proc ess of this invention are alkali metal borohydrides. These borohydrides decompose in the system and give oif gas at temperatures at which the blasting agent ingredients are formulated to produce a foamed product that is sensitized by small gas bubbles formed in the blasting agent. Any alkali metal borohydride can be used as the gasgenerating material in the present process. Representative alkali metal borohydrides that are used include lithium borohydride, potassium borohydride and sodium borohydride.
  • gas-generating material used in the process varies and the specific amount employed depends upon the desired final density of the resulting product and the temperature of the formulation when the gas-generating agent is added thereto. Generally, amounts ranging from about 0.002 to 0.10% by weight, preferably 0.01 to 0.06%, are incorporated into the mix.
  • the gas-generating agents are added to the composition at ordinary mixing temperatures, usually between to 170 F. However, for optimum results, the alkali metal borohydride gas-generating agent is added to the mix when the temperature of the mix is most favorable for decomposition of the foaming agent.
  • the inorganic oxidizing salts used in this invention are those conventionally used in water-bearing blasting agents and include ammonium, alkali metal and alkaline earth metal nitrates and perchlorates as well as mixtures of two or more such salts.
  • Representative inorganic oxidizing salts are ammonium nitrate, sodium nitrate, potassium nitrate, magnesium nitrate, calcium nitrate, ammonium perchlorate, sodium perchlorate, potassium perchlorate and magnesium perchlorate.
  • the amount of inorganic oxidizing salt used in the water-bearing blasting agents is from about 20 to about 75% by weight of the composition.
  • a mixture of inorganic nitrate salts is used of which at least about 45% by weight of the total composition is ammonium nitrate and of the order of 15 to 25%, preferably about 15%, based on the weight of the total composition, is sodium nitrate.
  • the foamed semisolid colloidal dispersion of water-bearing blasting agents can contain a thickening agent to gel the composition, thus forming the well-known blasting agents known as water gels or slurry explosives.
  • the amount of thickening agent added regulates the consistency of the blasting agent and such thickeners are used in amounts ranging from about 0.2 to Representative thickeners include galactomannans such as guar and locust bean gum; gum arabic; starches and modified starches such as dextrins, polyvinyl alcohol; polyacrylamides; high molecular weight polyethylene oxides; or mixtures of two or more of the above thickening agents. Best results are obtained when either guar gum or polyacrylamide is used as the thickener.
  • this invention is applicable to the production of water and oil emulsion-type water-bearing blasting agents.
  • These compositions contain, in addition to inorgamic oxidizing salt, water and fuel, and emulsifying agent.
  • the amount of emulsifying agent used is from about 0.5 to by weight, and preferably from about 1 to 2%. Larger quantities of emulsifying agent may be added since excess emulsifying agent merely serves as a supplemental fuel for the blasting agent.
  • the emulsifying agents used are those that form Water-in-oil emulsions, such as sorbitan fatty acid esters, e.g., soribtan monolaurate, palmitate or oleate; polyoxyethylene sorbitol esters and long chain fatty acids and esters thereof, so that a water-in-oil emulsion of the blasting agent is formed.
  • the emulsifying agent is a stearate salt, e.g., sodium stearate, alone or in combination with stearic acid.
  • emulsifying agents include sodium oleate with or without oleic acid, dodecylbenzene sulfonic acid and tall oil amides such as the tall oil amide of tetraethylene pentamide, EZ-Mul, manufactured by the Baroid Division of National Lead Co.
  • the fuel-s used in thickened water gel blasting agents include self-explosive fuels, nonexplosive fuels and metallic fuels as well as mixtures of the aforementioned types of fuels.
  • Representative self-explosive (fuels that can be used in the composition are organic nitrates, nitro compounds and nitra'mines such as trinitrotoluene, pentaerythritol tetranitrate, tetranitro-N-methylaniline, nitrostarch, explosive grade nitrocellulose, smokeless powder and mixtures thereof.
  • the amount of self-explosive fuel used is from 10 to 40% by weight, based on the weight of the composition.
  • Non-explosive fuels such as certain nitro aromatic hydrocarbons, for example, monoand dinitrobenzenes can be used, and sulfurous fuels including sulfur itself.
  • Carbonaceous fuels such as finely-divided coal, hydrocarbons such as fuel oil and paraflin wax, can be added to the composition.
  • Metallic fuels can also be used and these include light elements such as aluminum, magnesium, boron and silicon, both singly and in combination. Heavier metallic compounds and alloys including ferrophosphorus and ferrosilicon can be added to the mix.
  • Blasting agents of the emulsion type wherein a water and oil emulsion is formed must contain carbonaceous fuel that is liquid during formation of the emulsion.
  • the carbonaceous fuel is not soluble in water and generally forms the continuous phase of the emulsion so that the blasting agent is in the form of a water-in-oil emulsion.
  • the carbonaceous fuel that is emulsified when used in the emulsion type blasting agents can include oil alone, a wax and oil, a wax and a polymeric material, or a wax and a polymeric modified oil component.
  • the fuels used thus include hydrocarbons such as parafiinic, olefinic and aromatic that are saturted or unsaturated.
  • Waxes that can be used include paraffin wax and mineral waxes. Petroleum oil of varying viscosities can be used as the fuel, especially fuel oil such as No. 2 [fuel oil.
  • Polymeric materials such as natural or synthetic rubber may be used as a carbonaceous fuel component.
  • the fuel comprises oil alone.
  • the amount of fuel used is from about 3 to 10% by weight.
  • the emulsion type blasting agents can contain supplementary fuels, as disclosed hereinabove, especially par- 7 4 a ticulate metals, e.g., aluminum, and finely-divided coal.
  • the amount of fuel used in the blasting agents of the present invention is such that the oxygen balance of the blasting agent will be from 25 to +10% and preferably from 10 to +5
  • the amount of water used in the blasting agents of the thickened water gel and emulsion type is from 5 to 30 percent by weight, preferably, about from 10 to 25 percent by weight water is used in preparing thickened water gels and emulsion-type blasting agents.
  • nitrogen-base salts can be added to the water-bearing blasting agents to increase their effectiveness.
  • the nitrogen-base salt functions, among other things, as a fuel component, and such salts that are applicable to this invention are disclosed, for example, in U.S. Pat. 3,431,155.
  • the nitrogen-base salts used are monomethylammonium nitrate and ethylenediammonium dinitrate.
  • Such salts can be added to the composition in amounts of from about 5 to 40% by weight.
  • the composition can, and usually does, contain a crosslinking agent such as, for example, an alkali metal dichromate or a soluble antimony compound, e.g. potassium antimony tartrate, in amounts of from 0.001 to 1% by weight.
  • a crystal habit modifier for the inorganic oxidizing salt such as Petro AG, which is a derivative of naphthalene sulfonic acid salts, can also be added to water gel compositions, if desired.
  • the procedure for making thickened water gels is as follows. The oxidizer salts and other watersoluble materials are mixed with water at temperatures usually between about 140 and 170 F. to effect maximum solubility.
  • the remaining ingredients except thickener, crosslinking agent and gas-generating material, are added.
  • The-addition of these ingredients cools the mix.
  • the mixture is agitated briefly and thickener added. Mixing is continued until thickening occurs, generally about 4 minutes; the alkali metal borohydride gas-generating material is added and the temperature of the mix is preferably about from to 150 F.
  • the composition is mixed for about 30 seconds and then the crosslinking agent is added and a thickened [foamed blasting agent sensitized with gas bubbles is obtained.
  • a procedure'for making emulsion type blasting agents involves mixing the emulsifiable carbonaceous fuel and emulsifier at a temperature of about to 170 F. such that the fuel is liquified. Separately, the inorganic oxidizing salts and other water-soluble materials are dissolved in water at about 120 to 170 F., and the other materials (except for the liquid fuel/ emulsifier mix) admixed therein. To this aqueous mixture is added the liquid fuel/emulsifier mix to form a water and oil emulsion.
  • the temperature of the emulsion is usually about from 100 to F. or can be regulated therebetween, if desired; the emulsion begins to thicken and the gas-generating agent is added to the thickened emulsion.
  • EXAMPLE 1 Formulation: Percent by weight Water 15.4 Ammonium nitrate 48.4265 Sodium nitrate 15.0
  • the monomethylammonium nitrate fuel, 13/15 of the sodium nitrate and all of the ammonium nitrate were dissolved in water at 140 F.
  • the thickener was premixed With sugar and the balance of the sodium nitrate was added to the ammonium nitrate solution together with the sulfur and coal.
  • the mixture cooled to 100 F. as a result of the addition of the sodium nitrate as well as the result of heat loss by radiation, thickened, and sodium borohydride was added, followed by addition of the crosslinking agents.
  • the specific gravity of the resulting foamed water gel blasting agent stabilized at 1.25 at ambient temperature and remained at that level for at least 30 days.
  • EXAMPLE 2 EXAMPLE 3 Formulation: Percent by weight Ammonium nitrate 60.97 Water 17 Sodium nitrate 15 Fuel oil #2 EZ-Mul (tall oil amide of tetraethylene pentamine) 1 2 Ammonium nitrate, sodium nitrate and the tall oil amide of tetraethylene pentamine were mixed with the water at about 160 F. The fuel oil was added thereto when the mix was at 13O -140 F. and agitated to form a water-in-oil emulsion. The mixture started to thicken in about 2 minutes after agitation at which time the sodium borohydride was added to the thickened mix. Mixing was continued for about 1 minute to incorporate the foaming agent in the mix. The resulting water-in-oil emulsion blasting agent foamed and contained small gas bubbles of from about 20- to 100 microns in diameter. The blasting agent at 40 F. had a detonation velocity of about 5400 meters per second.
  • EXAMPLE 4 The procedure described above in Example 3 was repeated except that potassium borohydride was substituted in place of sodium borohydride, and the emulsifying agent used was 2% sodium stearate. The resulting foamed emulsion blasting agent contained small gas bubbles. The blasting agent detonated at 40 F. with a detonation velocity comparable to that obtained in Example 3.

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Abstract

MAKING FOAMED SEMISOLID COLLOIDAL DISPERSIONS OF WATER-BEARING BLASTING AGENTS CONTAINING AN INORGANIC OXIDIZING SALT, E.G., AMMONIUM NITRATE, FUEL, WATER AND ADDING THERTO AN ALKALI METAL BOROHYDRIDE GAS-GENERATING MATERTIAL THAT FOAMS AND SENSTIZES THE BLASTING AGENT.

Description

United States Patent US. Cl. 14922 21 Claims ABSTRACT OF THE DISCLOSURE Making foamed semisolid colloidal dispersions of water-bearing blasting agents containing an inorganic oxidizing salt, e.g., ammonium nitrate, fuel, water and adding thereto an alkali metal borohydride gas-generating material that foams and sensitizes the blasting agent.
BACKGROUND OF THE INVENTION Semisolid colloidal dispersions of water-bearing blasting agents are well known. These products typically comprise an oxidizing component, usually predominantly ammonium nitrate, a fuel component and water. More particularly, these blasting agents are referred to in the art as water-gels or slurry explosives, and emulsion type blasting agents. The blasting agents commonly referred to as water gels contain, in addition to the above ingredients, a thickening agent that gels the composition, e.g., guar gum or polyacrylamides. In addition, the water gels may contain high explosives such as TNT or metallic fuels such as aluminum that function not only as part of the fuel component of the blasting agent but also increase explosive strength. Representative water gels of the type disclosed hereinabove are more fully described in US. Pats. 3,153,606, 3,431,155 and 3,288,658. As indicated above, other water-bearing explosive compositions that are semisolid colloidal dispersions are known as emulsion type blasting agents. Emulsion type blasting agents contain at least one oxidizing agent, water, an emulsifying agent, and a fuel component that is a carbonaceous compound insoluble in water. The carbonaceous fuel used in the process for preparing these products is liquid during formation of the emulsion. The emulsifying agent generally forms a water-in-oil emulsion wherein oil is the continuous phase and water is the discontinuous phase of the emulsion. Representative water-bearing semisolid colloidal dispersions of emulsion type blasting agents are described in US. Pat. 3,447,978. Furthermore, these semisolid colloidal dispersions of water-bearing blasting agents, both the thickened water gel and emulsion type, have been prepared in such a manner that small gas bubbles are entrapped therein or they contain gas-entrapping material, e.g., microballoons. The inclusion of gas in the form of bubbles or in gas-entrapping material is known to regulate the strength of the blasting agent. Methods for preparing gas-containing water-bearing blasting agents include the mechanical incorporation of gas and in situ chemical generation of gas by the decomposition of certain compounds. Although these procedures have produced satisfactory products, there is a need for making foamed semisolid colloidal dispersions of water-bearing blasting agents by employing gas-generating chemical com ounds that are simple to use; inexpensive; form gas bubbles in the blasting agent within a short period of time which bubbles remain formed therein for extended periods of time; form gas bubbles in the composition that are small, generally the majority of bubbles are not greater than about 100 micron diameter, preferably between to 70 microns, for the most effective sensitivity; provide an effective control over the amount of gas introduced into the composition; and are applicable to waterice bearing blasting agents, e.g. water gels, and emulsiontype blasting agents.
SUMMARY OF THE INVENTION This invention provides a process for preparing foamed semisolid colloidal dispersions of Water-bearing blasting agents, especially water gels 0r thickened water-bearing explosives, and emulsion type blasting agents, which comprises mixing inorganic oxidizing salt, fuel and water, the improvement which comprises incorporating into the mix an alkali metal borohydride gas-generating material thereby foaming and sensitizing the blasting agent. When preparing water gels, a thickening agent, e.g., guar gum, is added to the water-bearing explosive composition in order to thicken or gel the aqueous phase. When emulion type blasting agents are prepared, an emulsifying agent and a liquid carbonaceous fuel are added to the water-bearing explosive during preparation in order to form an emulsion between the water and fuel. The amount of alkali metal borohydride added to the mix is about from 0.002 to 0.10% based on the weight of the total composition.
DESCRIPTION OF PREFERRED EMBODIMENTS The gas-generating materials that are used in the proc ess of this invention are alkali metal borohydrides. These borohydrides decompose in the system and give oif gas at temperatures at which the blasting agent ingredients are formulated to produce a foamed product that is sensitized by small gas bubbles formed in the blasting agent. Any alkali metal borohydride can be used as the gasgenerating material in the present process. Representative alkali metal borohydrides that are used include lithium borohydride, potassium borohydride and sodium borohydride. The exact amount of gas-generating material used in the process varies and the specific amount employed depends upon the desired final density of the resulting product and the temperature of the formulation when the gas-generating agent is added thereto. Generally, amounts ranging from about 0.002 to 0.10% by weight, preferably 0.01 to 0.06%, are incorporated into the mix. The gas-generating agents are added to the composition at ordinary mixing temperatures, usually between to 170 F. However, for optimum results, the alkali metal borohydride gas-generating agent is added to the mix when the temperature of the mix is most favorable for decomposition of the foaming agent. Best results are produced when the temperature of the composition during addition of alkali metal borohydride to the mix is from about to F, The alkali metal borohydride gas-generating material is added to water-gel type explosives after the mix has thickened, and to emulsion type blasting agents after the emulsion has formed, so that in each case the mix is sufiiciently viscous to retain gas bubbles when the composition foams and small gas bubbles form therein.
The inorganic oxidizing salts used in this invention are those conventionally used in water-bearing blasting agents and include ammonium, alkali metal and alkaline earth metal nitrates and perchlorates as well as mixtures of two or more such salts. Representative inorganic oxidizing salts are ammonium nitrate, sodium nitrate, potassium nitrate, magnesium nitrate, calcium nitrate, ammonium perchlorate, sodium perchlorate, potassium perchlorate and magnesium perchlorate. The amount of inorganic oxidizing salt used in the water-bearing blasting agents is from about 20 to about 75% by weight of the composition. Preferably, a mixture of inorganic nitrate salts is used of which at least about 45% by weight of the total composition is ammonium nitrate and of the order of 15 to 25%, preferably about 15%, based on the weight of the total composition, is sodium nitrate.
As mentioned above, the foamed semisolid colloidal dispersion of water-bearing blasting agents can contain a thickening agent to gel the composition, thus forming the well-known blasting agents known as water gels or slurry explosives. The amount of thickening agent added regulates the consistency of the blasting agent and such thickeners are used in amounts ranging from about 0.2 to Representative thickeners include galactomannans such as guar and locust bean gum; gum arabic; starches and modified starches such as dextrins, polyvinyl alcohol; polyacrylamides; high molecular weight polyethylene oxides; or mixtures of two or more of the above thickening agents. Best results are obtained when either guar gum or polyacrylamide is used as the thickener. In addition, as mentioned above, this invention is applicable to the production of water and oil emulsion-type water-bearing blasting agents. These compositions contain, in addition to inorgamic oxidizing salt, water and fuel, and emulsifying agent. The amount of emulsifying agent used is from about 0.5 to by weight, and preferably from about 1 to 2%. Larger quantities of emulsifying agent may be added since excess emulsifying agent merely serves as a supplemental fuel for the blasting agent. Generally the emulsifying agents used are those that form Water-in-oil emulsions, such as sorbitan fatty acid esters, e.g., soribtan monolaurate, palmitate or oleate; polyoxyethylene sorbitol esters and long chain fatty acids and esters thereof, so that a water-in-oil emulsion of the blasting agent is formed. Especially good results are obtained when the emulsifying agent is a stearate salt, e.g., sodium stearate, alone or in combination with stearic acid. Other emulsifying agents include sodium oleate with or without oleic acid, dodecylbenzene sulfonic acid and tall oil amides such as the tall oil amide of tetraethylene pentamide, EZ-Mul, manufactured by the Baroid Division of National Lead Co.
The fuel-s used in thickened water gel blasting agents include self-explosive fuels, nonexplosive fuels and metallic fuels as well as mixtures of the aforementioned types of fuels. Representative self-explosive (fuels that can be used in the composition are organic nitrates, nitro compounds and nitra'mines such as trinitrotoluene, pentaerythritol tetranitrate, tetranitro-N-methylaniline, nitrostarch, explosive grade nitrocellulose, smokeless powder and mixtures thereof. Generally, the amount of self-explosive fuel used is from 10 to 40% by weight, based on the weight of the composition. Non-explosive fuels such as certain nitro aromatic hydrocarbons, for example, monoand dinitrobenzenes can be used, and sulfurous fuels including sulfur itself. Carbonaceous fuels such as finely-divided coal, hydrocarbons such as fuel oil and paraflin wax, can be added to the composition. Metallic fuels can also be used and these include light elements such as aluminum, magnesium, boron and silicon, both singly and in combination. Heavier metallic compounds and alloys including ferrophosphorus and ferrosilicon can be added to the mix. Blasting agents of the emulsion type wherein a water and oil emulsion is formed must contain carbonaceous fuel that is liquid during formation of the emulsion. The carbonaceous fuel is not soluble in water and generally forms the continuous phase of the emulsion so that the blasting agent is in the form of a water-in-oil emulsion. The carbonaceous fuel that is emulsified when used in the emulsion type blasting agents can include oil alone, a wax and oil, a wax and a polymeric material, or a wax and a polymeric modified oil component. The fuels used thus include hydrocarbons such as parafiinic, olefinic and aromatic that are saturted or unsaturated. Waxes that can be used include paraffin wax and mineral waxes. Petroleum oil of varying viscosities can be used as the fuel, especially fuel oil such as No. 2 [fuel oil. Polymeric materials such as natural or synthetic rubber may be used as a carbonaceous fuel component. Preferably, the fuel comprises oil alone. Generally the amount of fuel used is from about 3 to 10% by weight. Optionally, the emulsion type blasting agents can contain supplementary fuels, as disclosed hereinabove, especially par- 7 4 a ticulate metals, e.g., aluminum, and finely-divided coal. In general, the amount of fuel used in the blasting agents of the present invention is such that the oxygen balance of the blasting agent will be from 25 to +10% and preferably from 10 to +5 The amount of water used in the blasting agents of the thickened water gel and emulsion type is from 5 to 30 percent by weight, preferably, about from 10 to 25 percent by weight water is used in preparing thickened water gels and emulsion-type blasting agents.
Optionally, other ingredients can be incorporated in the blasting agents. For example, nitrogen-base salts can be added to the water-bearing blasting agents to increase their effectiveness. The nitrogen-base salt functions, among other things, as a fuel component, and such salts that are applicable to this invention are disclosed, for example, in U.S. Pat. 3,431,155. Preferably, the nitrogen-base salts used are monomethylammonium nitrate and ethylenediammonium dinitrate. Such salts can be added to the composition in amounts of from about 5 to 40% by weight. As is conventional in the preparation of thickened water gels, the composition can, and usually does, contain a crosslinking agent such as, for example, an alkali metal dichromate or a soluble antimony compound, e.g. potassium antimony tartrate, in amounts of from 0.001 to 1% by weight. Likewise, a crystal habit modifier for the inorganic oxidizing salt such as Petro AG, which is a derivative of naphthalene sulfonic acid salts, can also be added to water gel compositions, if desired. Generally, the procedure for making thickened water gels is as follows. The oxidizer salts and other watersoluble materials are mixed with water at temperatures usually between about 140 and 170 F. to effect maximum solubility. Then the remaining ingredients, except thickener, crosslinking agent and gas-generating material, are added. The-addition of these ingredients cools the mix. Subsequently, the mixture is agitated briefly and thickener added. Mixing is continued until thickening occurs, generally about 4 minutes; the alkali metal borohydride gas-generating material is added and the temperature of the mix is preferably about from to 150 F. The composition is mixed for about 30 seconds and then the crosslinking agent is added and a thickened [foamed blasting agent sensitized with gas bubbles is obtained.
A procedure'for making emulsion type blasting agents involves mixing the emulsifiable carbonaceous fuel and emulsifier at a temperature of about to 170 F. such that the fuel is liquified. Separately, the inorganic oxidizing salts and other water-soluble materials are dissolved in water at about 120 to 170 F., and the other materials (except for the liquid fuel/ emulsifier mix) admixed therein. To this aqueous mixture is added the liquid fuel/emulsifier mix to form a water and oil emulsion. Preferably at this point in the procedure the temperature of the emulsion is usually about from 100 to F. or can be regulated therebetween, if desired; the emulsion begins to thicken and the gas-generating agent is added to the thickened emulsion.
The following examples further illustrate the invention in detail.
EXAMPLE 1 Formulation: Percent by weight Water 15.4 Ammonium nitrate 48.4265 Sodium nitrate 15.0
Monomethylammonium nitrate 10.3 Sugar 2.0 Sulfur 5.0 Coal 3.0 Thickener (guar gum) 0.8 Sodium borohydride 0.036 Crosslinking agent:
Sodium dichromate 0.03 Potassium antimony tartrate 0.0075
The monomethylammonium nitrate fuel, 13/15 of the sodium nitrate and all of the ammonium nitrate were dissolved in water at 140 F. The thickener was premixed With sugar and the balance of the sodium nitrate was added to the ammonium nitrate solution together with the sulfur and coal. The mixture, cooled to 100 F. as a result of the addition of the sodium nitrate as well as the result of heat loss by radiation, thickened, and sodium borohydride was added, followed by addition of the crosslinking agents.
The specific gravity of the resulting foamed water gel blasting agent stabilized at 1.25 at ambient temperature and remained at that level for at least 30 days. The foamed explosive composition detonated at 40 F. in 6-inchdiameter (unconfined) at a velocity of 3810 meters/sec. Gas bubbles in the foamed composition were 20 to 100 microns in diameter.
EXAMPLE 2 EXAMPLE 3 Formulation: Percent by weight Ammonium nitrate 60.97 Water 17 Sodium nitrate 15 Fuel oil #2 EZ-Mul (tall oil amide of tetraethylene pentamine) 1 2 Ammonium nitrate, sodium nitrate and the tall oil amide of tetraethylene pentamine were mixed with the water at about 160 F. The fuel oil was added thereto when the mix was at 13O -140 F. and agitated to form a water-in-oil emulsion. The mixture started to thicken in about 2 minutes after agitation at which time the sodium borohydride was added to the thickened mix. Mixing was continued for about 1 minute to incorporate the foaming agent in the mix. The resulting water-in-oil emulsion blasting agent foamed and contained small gas bubbles of from about 20- to 100 microns in diameter. The blasting agent at 40 F. had a detonation velocity of about 5400 meters per second.
EXAMPLE 4 The procedure described above in Example 3 was repeated except that potassium borohydride was substituted in place of sodium borohydride, and the emulsifying agent used was 2% sodium stearate. The resulting foamed emulsion blasting agent contained small gas bubbles. The blasting agent detonated at 40 F. with a detonation velocity comparable to that obtained in Example 3.
I claim:
1. In a process for preparing foamed semisolid colloidal dispersions of water-bearing blasting agents comprising mixing inorganic oxidizing salt, fuel and water, the improvement which comprises incorporating into the mix an alkali metal borohydride gas-generating material that foams and sensitizes the blasting agent.
2. In a process for preparing foamed semisolid colloidal dispersions of water-bearing blasting agents comprising mixing inorganic oxidizing salt, fuel, thickener Sodium borohydride 6 and water, the improvement which comprises incorporating into the mix an alkali metal borohydride gas-generating material that foams and sensitizes the thickened blasting agent.
3. The process of claim 2 wherein the gas-generating material is sodium borohydride.
4. The process of claim 2 wherein the amount of sodium borohydride added is about from 0.002 to 0.10% by weight.
5. The process of claim 2 wherein the amount of sodium borohydride added is about from 0.01 to 0.06% by weight.
6. The process of claim 3 wherein the thickener is polyacrylamide.
7. The process of claim 3 wherein the thickener is guar gum.
8. The process of claim 3 wherein the inorganic oxidizing salt is ammonium nitrate.
9. The process of claim 3 wherein the mix is at a temperature of about from to F. when the gasgenerating material is added thereto.
10. The process of claim 3 wherein a nitrogen-base salt is added to the mix.
11. The process of claim 10 wherein the nitrogen-base salt is monomethylammonium nitrate.
12. In a process for preparing foamed semisolid colloidal dispersions of water-bearing blasting agents comprising mixing inorganic oxidizing salt, liquid carbonaceous fuel, emulsifying agent and water, the improvement which comprises incorporating into the mix an alkali metal borohydride gas-generating material that foams and sensitizes the emulsified blasting agent.
13. The process of claim 12 wherein the emulsifying agent is one that form a water-in-oil emulsion.
14. The process of claim 13 wherein the gas-generating material is sodium borohydride.
15. The process of claim 14 wherein the amount of sodium borohydride added is about from 0.002 to 0.10% by weight.
16. The process of claim 14 wherein the amount of sodium borohydride added is about from 0.01 to 0.06% by weight.
17. The process of claim 14 wherein the fuel is fuel oil.
18. The process of claim 14 wherein the inorganic oxidizing salt contains ammonium nitrate.
19. The process of claim 14 wherein the mix is at a temperature of about from 100 to 150 F. when the gas-generating material is added thereto.
20. The process of claim 18 wherein the inorganic oxidizing salt contains sodium nitrate.
21. The process of claim 14 wherein the emulsifying agent is a stearate salt.
References Cited UNITED STATES PATENTS 3,282,752 11/1966 Clay et al. 14922 3,347,722 lO/1967 Gordon 149-44 3,383,399 5/1968 Stafiej et al. 14922 3,390,032 6/1968 Albert 149-60 3,445,305 5/1969 Lyerly 149-44 3,471,346 10/1969 Lyerly 149 -60 3,522,117 7/1970 Atadan et al. 14960 CARL D. QUARFORTH, Primary Examiner E. A. MILLER, Assistant Examiner US. Cl. X.R.
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Cited By (16)

* Cited by examiner, † Cited by third party
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US3926698A (en) * 1974-02-21 1975-12-16 Ireco Chemicals Explosive compositions containing metallic fuel particles and method of preparation thereof
US4008108A (en) * 1975-04-22 1977-02-15 E. I. Du Pont De Nemours And Company Formation of foamed emulsion-type blasting agents
FR2323654A1 (en) * 1975-09-11 1977-04-08 Int Constr Prod Res PROCEDURE AND COMPOSITION FOR CONTROLLING THE REMOVAL OF CEMENT MASS DURING SETTING, BY ADDITION OF AGENTS EMITTING GAS
US4453989A (en) * 1982-04-05 1984-06-12 Atlas Powder Company Solid sensitizers for water-in-oil emulsion explosives
US4737207A (en) * 1985-12-23 1988-04-12 Nitro Nobel Ab Method for the preparation of a water-in-oil type emulsion explosive and an oxidizer composition for use in the method
US4933028A (en) * 1989-06-30 1990-06-12 Atlas Powder Company High emulsifier content explosives
US4980000A (en) * 1990-01-17 1990-12-25 Atlas Powder Company Nitrostarch emulsion explosives production process
US5051142A (en) * 1990-01-17 1991-09-24 Atlas Powder Company Emulsion explosive containing nitrostarch
US5089652A (en) * 1990-01-17 1992-02-18 Atlas Powder Company Nitrate ester preparation
FR2670203A1 (en) * 1990-12-10 1992-06-12 Dantex Explosives AQUEOUS EXPLOSIVE COMPOSITION CONTAINING GAS BUBBLES STABILIZED WITH RESPECT TO MIGRATION AND AGGLOMERATION.
US6537399B2 (en) 1997-06-26 2003-03-25 Union Espanola De Explosivos, S.A. Process and mechanism for in situ sensitization of aqueous explosives
US6610158B2 (en) 1999-07-09 2003-08-26 Union Espanola De Explosivos, S.A. Procedure and installation for on-site manufacturing of explosives made from a water based oxidizing product
US20040016481A1 (en) * 2002-06-26 2004-01-29 Union Espanola De Explosivos, A Spanish Corporation Process for the "in situ" manufacturing of explosive mixtures
US20090301619A1 (en) * 2005-10-26 2009-12-10 Newcastle Innovation Limited Gassing of emulsion explosives with nitric oxide
US20110132505A1 (en) * 2007-01-10 2011-06-09 Newcastle Innovation Limited Method for gassing explosives especially at low temperatures
EP3556741A1 (en) 2018-04-16 2019-10-23 Maxamcorp Holding, S.L. Procedure and installation for loading boreholes with bulk water-based suspension or watergel type explosives

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3926698A (en) * 1974-02-21 1975-12-16 Ireco Chemicals Explosive compositions containing metallic fuel particles and method of preparation thereof
US4008108A (en) * 1975-04-22 1977-02-15 E. I. Du Pont De Nemours And Company Formation of foamed emulsion-type blasting agents
FR2323654A1 (en) * 1975-09-11 1977-04-08 Int Constr Prod Res PROCEDURE AND COMPOSITION FOR CONTROLLING THE REMOVAL OF CEMENT MASS DURING SETTING, BY ADDITION OF AGENTS EMITTING GAS
US4453989A (en) * 1982-04-05 1984-06-12 Atlas Powder Company Solid sensitizers for water-in-oil emulsion explosives
US4737207A (en) * 1985-12-23 1988-04-12 Nitro Nobel Ab Method for the preparation of a water-in-oil type emulsion explosive and an oxidizer composition for use in the method
US4933028A (en) * 1989-06-30 1990-06-12 Atlas Powder Company High emulsifier content explosives
US4980000A (en) * 1990-01-17 1990-12-25 Atlas Powder Company Nitrostarch emulsion explosives production process
US5051142A (en) * 1990-01-17 1991-09-24 Atlas Powder Company Emulsion explosive containing nitrostarch
US5089652A (en) * 1990-01-17 1992-02-18 Atlas Powder Company Nitrate ester preparation
ES2051183A1 (en) * 1990-12-10 1994-06-01 Dantex Explosives explosive composition
FR2670203A1 (en) * 1990-12-10 1992-06-12 Dantex Explosives AQUEOUS EXPLOSIVE COMPOSITION CONTAINING GAS BUBBLES STABILIZED WITH RESPECT TO MIGRATION AND AGGLOMERATION.
US6537399B2 (en) 1997-06-26 2003-03-25 Union Espanola De Explosivos, S.A. Process and mechanism for in situ sensitization of aqueous explosives
US6610158B2 (en) 1999-07-09 2003-08-26 Union Espanola De Explosivos, S.A. Procedure and installation for on-site manufacturing of explosives made from a water based oxidizing product
US20040016481A1 (en) * 2002-06-26 2004-01-29 Union Espanola De Explosivos, A Spanish Corporation Process for the "in situ" manufacturing of explosive mixtures
US6949153B2 (en) 2002-06-26 2005-09-27 Union Espanola De Explosivos S.A. Process for the “in situ” manufacturing of explosive mixtures
US20090301619A1 (en) * 2005-10-26 2009-12-10 Newcastle Innovation Limited Gassing of emulsion explosives with nitric oxide
US8114231B2 (en) 2005-10-26 2012-02-14 Newcastle Innovation Limited Gassing of emulsion explosives with nitric oxide
US20110132505A1 (en) * 2007-01-10 2011-06-09 Newcastle Innovation Limited Method for gassing explosives especially at low temperatures
EP3556741A1 (en) 2018-04-16 2019-10-23 Maxamcorp Holding, S.L. Procedure and installation for loading boreholes with bulk water-based suspension or watergel type explosives
WO2019201851A1 (en) 2018-04-16 2019-10-24 Maxamcorp Holding, S.L. Procedure and installation for loading boreholes with bulk water-based suspension or watergel type explosives

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