US2630379A - Method of improving the waterresistance of ammonium nitrate explosives - Google Patents

Method of improving the waterresistance of ammonium nitrate explosives Download PDF

Info

Publication number
US2630379A
US2630379A US121457A US12145749A US2630379A US 2630379 A US2630379 A US 2630379A US 121457 A US121457 A US 121457A US 12145749 A US12145749 A US 12145749A US 2630379 A US2630379 A US 2630379A
Authority
US
United States
Prior art keywords
water
reaction product
ammonium nitrate
formaldehyde
percent
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
US121457A
Inventor
William C Lytle
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.)
Atlas Powder Co
Original Assignee
Atlas Powder Co
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 Atlas Powder Co filed Critical Atlas Powder Co
Priority to US121457A priority Critical patent/US2630379A/en
Priority to GB24706/50A priority patent/GB674517A/en
Application granted granted Critical
Publication of US2630379A publication Critical patent/US2630379A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C06—EXPLOSIVES; MATCHES
    • C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B31/00—Compositions containing an inorganic nitrogen-oxygen salt
    • C06B31/28—Compositions containing an inorganic nitrogen-oxygen salt the salt being ammonium nitrate
    • C06B31/30—Compositions containing an inorganic nitrogen-oxygen salt the salt being ammonium nitrate with vegetable matter; with resin; with rubber

Definitions

  • the present invention relates to a method of forming an explosive composition possessing advantageous properties, and, more particularly, it relates to a method of improving the water resistance of an ammonium nitrate explosive composition.
  • ammonium nitrate has been employed in explosive compositions and in fact today it is the principal power-producing ingredient present in most commercial explosives, for example, it is employed in the so-called ammonia dynamites in which ammonium nitrate in ammonium nitrate may actually be leached from the explosive product.
  • nitro cotton has been included in the compositions; the salt has been coated with water-repellent materials such as paraffin, petrolatum, and rosin; and various water-dispersible starch materials, which form a protective gel with water, have been included in the compositions.
  • One object of the present invention is to provide a method of forming a water-resistant explosive composition containing ammonium nitrate and possessing advantageous properties.
  • a more specific object of the present invention is the provision of a method of forming an ammonia dynamite characterized by resistance to the moisture and water with which the product will come in contact during the normal use thereof.
  • Still another object is to provide a method of forming an ammonium nitrate-containing explosive composition rendered water-resistant by the inclusion therein of an additive material which does not decrease the sensitiveness or stability of the explosive or otherwise affect the desired properties thereof.
  • the explosive composition comprises ammonium nitrate in granular form having admixed therewith and uniformly distributed throughout the mass thereof, a finely divided solid, hydrophilic urea-formaldehyde type reaction product.
  • ammonium nitrate and ureaformaldehyde type reaction product there will also be present in the explosive composition such other ingredients as are usually employed, depending upon the type of explosive desired.
  • solid, hydrophilic urea-formaldehyde type reaction product as used herein includes the solid hydrophilic reaction products of formaldehyde and at least one of the amino compounds selected from the group consisting of urea, thiourea, and melamine.
  • reaction products may be obtained as simple chemical products which may be crystalline, such as dimethylolurea, using the urea-formaldehyde reaction products as typical; or they may be obtained as resinous solids, in which case the reaction products are partially condensed or polymerized but still possess hydrophilic properties (hereinafter referred to as partially polymerized)
  • a reaction product is selected which is completely soluble in water.
  • the reaction product employed is convertible into a hydrophobic product and when converted the resin is substantially infusible and insoluble in the usual solvents.
  • This characteristic of convertibility from the hydrophilic to the hydrophobic state is possessed both by the simple chemical products and by the partially polymerized resinous products, used in carrying out the method of forming an explosive composition in accordance with the present invention.
  • the hydrophilic products are converted into the hydrophobic resin by the use of a catalyst providing acid, with or without the application of heat, depending upon the particular catalyst and reaction product.
  • catalysts are acids, acid salts, ammonium salts of strong acids, and the like.
  • the convertibility of the product indicates its applicability for use in carrying out the method of forming an explosive product in accordance with the present invention and, as discussed hereinafter, the water-resistance provided may be due to the conversion of the reaction product.
  • the reaction product may be a conjoint reaction product of two or more of the amino compounds with the formaldehyde, for example, a reaction product between urea, melamine, and formaldehyde or between urea, thiourea, and formaldehyde.
  • a reaction product between urea, melamine, and formaldehyde or between urea, thiourea, and formaldehyde is preferred.
  • the reaction product may or may not contain a catalyst and satisfactory water-resistance is imparted to the explosive composition in both instances.
  • the reaction product may contain finely divided fillers such as wood flour or starch, but the use of a reaction product free from such materials is preferred.
  • the ratio of amino compound to formaldehyde in the reaction product is immaterial so long as the reaction product is obtainable as solid material capable of being subdivided, possesses hydrophilic properties and is convertible to a hydrophobic resinous product, and the adjustment of the ratios of the formaldehyde and the amino compound or compounds used in'the preparation of the reaction products is within the skill of the art.
  • the mol ratio of formaldehyde to urea employed will vary from 1.05 to 1 through 2 to 1 (the ratio in dimethylolurea) to about 2.7 to 1, and in the preferred embodiment, the mol ratio of formaldehyde to urea will be between about 1.2 to 1 and about 1.5 to 1. When thiourea is used, the same ratios are applicable.
  • the mol ratios of formaldehyde to melamine may be between somewhat above 1, prefably above 2, to 1 and about 6 to 1, and in the preferred embodiment the ratio will be between about 2 mols of formaldehyde to 1 of melamine and about 3 mols of formaldehyde to 1 of melamine.
  • the amounts will also be adjusted to obtain a reaction product of the stated properties.
  • Examplesof the partially polymerized-resinous products which may be used in carrying out the method of forming an explosive composition in accordance with the present invention are the dry, powdered, water-soluble urea-formaldehyde, melamine-formaldehyde or urea-melamine-formaldehyde resinous products sold on the market as resin glues for use in adhesives particularly for the binding of plywood, veneers, furniture, and the like.
  • the desired protection is afforded by a reaction product which does not contain a catalyst, as well as by one that does, and if it is a conversion that provides the desired water-resistance, the ammonium nitrate, or the ammonium chloride usually occluded therewith, serves as the catalyst when a catalystfree reaction product is employed. Regardless of the reason for the results obtained, the presence of the finely divided reaction product admixed with the ammonium nitrate particles provides the desired water-resistance to the explosive composition as may be seen from the table hereinafter set forth.
  • the reaction product is employed insolid, finely divided form, for example, the particle size is generally such that the material will pass through a mesh screen, preferably through a mesh screen.
  • care is exercised to assure that the subdivided reaction product is uniformly distributed throughout the explosive composition.
  • the ammonium nitrate employed may be of any desired particle size, for example, in the caseof the explosive composition in an ammonia dynamite, the ammonium nitrate may be present either as coarse and fine particles or both, for example, in the case of coarse ammonium nitrate at least 60% will be retained on a U. S. S. No. 35 screen, whereas in the use of line ammonium nitrate at least 95% will pass a U. S. S. No. 35 screen.
  • the ammonium nitrate particles may, ifdesired, be coated with a waterrepellent material, for example, wax or a mixture of parafhn and petrolatum.
  • the explosive composition will comprise, in addition to the ammonium nitrate and the reaction product, other usual ingredients depending upon the type of explosive composition desired. So far as the other components of; the explosive composition and the proportions thereof are concerned, the usual practices of the art may be employed. Likewise, the explosive composition may be of any desired density and may be packaged in any suitablecasing or shell; In view of the fact that except for the inclusion of the water-resistanceimparting reaction product, the-composition may be varied in accordance with the skill of the art, it is not necessary to discuss in detail the other components which may be present in the composition.
  • reaction product is advantageous in any explosive composition containing ammonium nitrate, it is especially advantageous for use in an ammonia dynamite, and for this reason further reference will be made to the preferred embodiment of the inventionwherein' the explosive composition is an ammonia dynamite.
  • Ammonia dynamites in addition to the ammonium nitrate, contain a sensitizing material and a solid fuel.
  • the sensitizing agent maybe an explosive liquid nitric ester typified by nitroglycerine or it may be an explosive nitro aromatic compound such as trinitrotoluene, trinitronaphthalene, and the like or mixtures thereof.
  • the explosive composition contains nitroglycerine which may be relatively pure nitroglycerine or may be a nitrated mixture of glycerine, ethyleneglycohand corn or can elsugar or other nitratable substance, as is usually employed in the art.
  • nitroglycerine The aforesaid nitrated mixture, as well as relatively pure nitroglycerine, is designated in the trade as nitroglycerine, and that term is used herein to include both materials.
  • the amount of nitroglycerine will vary, depending upon the properties desired and the other ingredients present, but is usually employed between and 20% by weight of the total weight of the composition.
  • the explosive composition will comprise at least about 6% of nitroglycerine.
  • the solid fuel may be any one or more of a wide variety of materials. for example, wood pulp, bagasse, ivory nut "meal, ground walnut shells, apricot pit pulp, a flour such as corn flour, charcoal, coal, sulphur, and the like, and usually the solid fuel will be present in an amount between about 4% and about 15%.
  • ammonia dynamites usually, or at times, contain other materials, for example, nitro cotton, sodium nitrate, and an antacid such as calcium carbonate (chalk), magnesium carbonate, or the like. Any or all of these materials as well as other ingredients may be present in the explosive composition of the invention in proportions to provide an explosive of the desired characteristics, all as is well known in the art.
  • the reaction product employed will be sufiicient to provide the desired water-resistance and usually will be present in an amount between about and about 5%, preferably between about 1 and about 3%, based on the total weight of the 6 explosive composition, although amounts in excess of these figures and over that required for water-resistance may be employed without disadvantageous efiects.
  • Ammonium nitrate explosive compositions were prepared by conventional procedures to each of the formulae listed in the tables hereinafter set forth in which were incorporated, in accordance with the present invention, a reaction product of the type and in the amount specified in said tables.
  • Each of these explosive compositions were packed in conventional $4 x 8" paper cartridges. The ends of the cartridges were sealed with tallow. The wrapper of each of the cartridges was perforated with sixteen 4" holes arranged in four lines parallel to the axis and equidistantly spaced around the cartridge, the holes in adjacent rows being staggered. .Each cartridge was placed in a vessel, was covered with sand, and water was poured into the vessel until it stood above the sand. The cartridge was then removed from the sand after a known number of hours. and its detonability with a No. 6 blasting cap was determined.
  • Melmac 401f a water-soluble melamine-formaldehyde reaction product in the form of a dry powder and containing; no filler and a very small amount, if any, of catalyst, sold by American Cyanamid and Chemical Corp.
  • Melmac 40 a :water-soluble melamine-formaldehyde reaction product in the form of a dry powder and containing no filler and a very small amount, if any, of catalyst, sold by American Cyanamid and Chemical Corp.
  • the water-resistance 01 this explosive compositioncontoining no reaction product was: D-3;
  • an explosive composition comprising a mixture of granular ammonium nitrate, a sensitizer and a solid fuel which comprises intimately mixing with and substantially uniformly distributing throughout said mixture of granular ammonium nitrate, sensitizer and solid fuel, a solid, finely-divided hydrophilic reaction product of formaldehyde and at least one of the amino compounds selected from the group consisting of urea, thio'urea and melamine.
  • reaction product is a water-soluble partially polymerized urea-formaldehyde resin and is in an amount between about 0.5% and about 5% based on the weight of the explosive composition.
  • reaction product is a water-soluble partially polymerized melamine-formaldehyde resin and is in an amount between about 0.5% and about 5% based on the weight of the explosive composition.
  • reaction product is a water-soluble partially polymerized urea-melamine-formaldehyde resin and is in an amount between about 0.5% and about 5% based on the weight of the explosive composition.
  • an explosive composition comprising a mixture of granular ammonium nitrate, at least one sensitizer selected from the group consisting of an explosive liquid nitric ester and a nitro aromatic compound, and a solid carbonaceous fuel which comprises intimately mixing with and substantially uniformly distributing throughout said mixture of granular ammonium nitrate, sensitizer and solid fuel, a solid, finely-divided hydrophilic reaction product of formaldehyde and at least one of the amino compounds selected from the group consisting of urea, thiourea and melamine.
  • the sensitizer is nitroglycerin and is in an amount between about 6% and about 20% based on the weight of the explosive composition; and wherein said reaction product is a water-soluble partially polymerized urea-formaldehyde resin in an amount between about 0.5% and about 5% based on the weight of the explosive composition.
  • the sensitizer is nitroglycerin and is in an amount between about 6% and about 20% based on the weight of the explosive composition; and wherein the reaction product is a water-soluble partially polymerized melamine-formaldehyde resin in an amount between about 0.5% and about 5% based on the Weight of the explosive composition.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Chemical And Physical Treatments For Wood And The Like (AREA)

Description

Patented Mar. 3, 1953 UNITED STATES OFFICE METHOD OF IIWPROVING THE WATER- RESISTANCE F AMMONIUM NITRATE EXPLOSIVES No Drawing. Application October 14, 1949, Serial No. 121,457
9 Claims. 1
The present invention relates to a method of forming an explosive composition possessing advantageous properties, and, more particularly, it relates to a method of improving the water resistance of an ammonium nitrate explosive composition.
For years, ammonium nitrate has been employed in explosive compositions and in fact today it is the principal power-producing ingredient present in most commercial explosives, for example, it is employed in the so-called ammonia dynamites in which ammonium nitrate in ammonium nitrate may actually be leached from the explosive product.
Several methods for improving the water-resistance of explosive compositions containing ammonium nitrate have heretofore been used with various degrees of success, for example, nitro cotton has been included in the compositions; the salt has been coated with water-repellent materials such as paraffin, petrolatum, and rosin; and various water-dispersible starch materials, which form a protective gel with water, have been included in the compositions.
One object of the present invention is to provide a method of forming a water-resistant explosive composition containing ammonium nitrate and possessing advantageous properties.
A more specific object of the present invention is the provision of a method of forming an ammonia dynamite characterized by resistance to the moisture and water with which the product will come in contact during the normal use thereof.
Still another object is to provide a method of forming an ammonium nitrate-containing explosive composition rendered water-resistant by the inclusion therein of an additive material which does not decrease the sensitiveness or stability of the explosive or otherwise affect the desired properties thereof.
Other objects will be apparent from a consideration of this specification and the claims.
In accordance with the present invention, the explosive composition comprises ammonium nitrate in granular form having admixed therewith and uniformly distributed throughout the mass thereof, a finely divided solid, hydrophilic urea-formaldehyde type reaction product. In addition to the ammonium nitrate and ureaformaldehyde type reaction product, there will also be present in the explosive composition such other ingredients as are usually employed, depending upon the type of explosive desired.
The term solid, hydrophilic urea-formaldehyde type reaction product as used herein includes the solid hydrophilic reaction products of formaldehyde and at least one of the amino compounds selected from the group consisting of urea, thiourea, and melamine. As is well known, such reaction products may be obtained as simple chemical products which may be crystalline, such as dimethylolurea, using the urea-formaldehyde reaction products as typical; or they may be obtained as resinous solids, in which case the reaction products are partially condensed or polymerized but still possess hydrophilic properties (hereinafter referred to as partially polymerized) Preferably, a reaction product is selected which is completely soluble in water.
The reaction product employed is convertible into a hydrophobic product and when converted the resin is substantially infusible and insoluble in the usual solvents. This characteristic of convertibility from the hydrophilic to the hydrophobic state is possessed both by the simple chemical products and by the partially polymerized resinous products, used in carrying out the method of forming an explosive composition in accordance with the present invention. As is well known, the hydrophilic products are converted into the hydrophobic resin by the use of a catalyst providing acid, with or without the application of heat, depending upon the particular catalyst and reaction product. Examples of catalysts are acids, acid salts, ammonium salts of strong acids, and the like. The convertibility of the product indicates its applicability for use in carrying out the method of forming an explosive product in accordance with the present invention and, as discussed hereinafter, the water-resistance provided may be due to the conversion of the reaction product.
The reaction product may be a conjoint reaction product of two or more of the amino compounds with the formaldehyde, for example, a reaction product between urea, melamine, and formaldehyde or between urea, thiourea, and formaldehyde. Of the products available for use, a partially polymerized water-soluble urea-formaldehyde or melamine-formaldehyde or ureamelamine-formaldehyde product is preferred. The reaction product may or may not contain a catalyst and satisfactory water-resistance is imparted to the explosive composition in both instances. In addition, the reaction product may contain finely divided fillers such as wood flour or starch, but the use of a reaction product free from such materials is preferred.
The ratio of amino compound to formaldehyde in the reaction product is immaterial so long as the reaction product is obtainable as solid material capable of being subdivided, possesses hydrophilic properties and is convertible to a hydrophobic resinous product, and the adjustment of the ratios of the formaldehyde and the amino compound or compounds used in'the preparation of the reaction products is within the skill of the art. Usually, the mol ratio of formaldehyde to urea employed will vary from 1.05 to 1 through 2 to 1 (the ratio in dimethylolurea) to about 2.7 to 1, and in the preferred embodiment, the mol ratio of formaldehyde to urea will be between about 1.2 to 1 and about 1.5 to 1. When thiourea is used, the same ratios are applicable. amine, the mol ratios of formaldehyde to melamine may be between somewhat above 1, prefably above 2, to 1 and about 6 to 1, and in the preferred embodiment the ratio will be between about 2 mols of formaldehyde to 1 of melamine and about 3 mols of formaldehyde to 1 of melamine. In the case of urea-melamine-formaldehyde reaction products, the amounts will also be adjusted to obtain a reaction product of the stated properties.
Examplesof the partially polymerized-resinous products which may be used in carrying out the method of forming an explosive composition in accordance with the present invention are the dry, powdered, water-soluble urea-formaldehyde, melamine-formaldehyde or urea-melamine-formaldehyde resinous products sold on the market as resin glues for use in adhesives particularly for the binding of plywood, veneers, furniture, and the like. Typical of such products are Uformite (Resinous Products Chemical Company); Plaskon Resin Glue (Plaskon Division of Libbey-Owens-Ford Glass Company); Cascamite (Casein Company of America); and *Melmac and Melurac (American Cyanamid and Chemical Corporation). Likewise commercial hydrophilic, convertible molding compositions sold by the stated or other companies may be used, if desired.
The reason why water-resistance is provided by the reaction product is not fully understood, and it may be due merely to the fact that, when moisture or water comes into contact with the product, the hydrophilic reaction product absorbs the moisture or water and'possiblyswells to protect the ammonium nitrate, but there is some In the case of mel-.
indication that there is a conversion of the reaction product from the hydrcphilic state to the hydrophobic state. As pointed out above, the desired protection is afforded by a reaction product which does not contain a catalyst, as well as by one that does, and if it is a conversion that provides the desired water-resistance, the ammonium nitrate, or the ammonium chloride usually occluded therewith, serves as the catalyst when a catalystfree reaction product is employed. Regardless of the reason for the results obtained, the presence of the finely divided reaction product admixed with the ammonium nitrate particles provides the desired water-resistance to the explosive composition as may be seen from the table hereinafter set forth.
As referred to above, the reaction product is employed insolid, finely divided form, for example, the particle size is generally such that the material will pass through a mesh screen, preferably through a mesh screen. In making the explosive composition, care is exercised to assure that the subdivided reaction product is uniformly distributed throughout the explosive composition.
The ammonium nitrate employed may be of any desired particle size, for example, in the caseof the explosive composition in an ammonia dynamite, the ammonium nitrate may be present either as coarse and fine particles or both, for example, in the case of coarse ammonium nitrate at least 60% will be retained on a U. S. S. No. 35 screen, whereas in the use of line ammonium nitrate at least 95% will pass a U. S. S. No. 35 screen. The ammonium nitrate particles may, ifdesired, be coated with a waterrepellent material, for example, wax or a mixture of parafhn and petrolatum.
As stated above, the explosive composition will comprise, in addition to the ammonium nitrate and the reaction product, other usual ingredients depending upon the type of explosive composition desired. So far as the other components of; the explosive composition and the proportions thereof are concerned, the usual practices of the art may be employed. Likewise, the explosive composition may be of any desired density and may be packaged in any suitablecasing or shell; In view of the fact that except for the inclusion of the water-resistanceimparting reaction product, the-composition may be varied in accordance with the skill of the art, it is not necessary to discuss in detail the other components which may be present in the composition. While the use of the reaction productis advantageous in any explosive composition containing ammonium nitrate, it is especially advantageous for use in an ammonia dynamite, and for this reason further reference will be made to the preferred embodiment of the inventionwherein' the explosive composition is an ammonia dynamite.
Ammonia dynamites, in addition to the ammonium nitrate, contain a sensitizing material and a solid fuel. The sensitizing agent maybe an explosive liquid nitric ester typified by nitroglycerine or it may be an explosive nitro aromatic compound such as trinitrotoluene, trinitronaphthalene, and the like or mixtures thereof. In the preferred embodiment of the invention, the explosive composition contains nitroglycerine which may be relatively pure nitroglycerine or may be a nitrated mixture of glycerine, ethyleneglycohand corn or can elsugar or other nitratable substance, as is usually employed in the art. The aforesaid nitrated mixture, as well as relatively pure nitroglycerine, is designated in the trade as nitroglycerine, and that term is used herein to include both materials. In an ammonia dynamite, the amount of nitroglycerine will vary, depending upon the properties desired and the other ingredients present, but is usually employed between and 20% by weight of the total weight of the composition. In the preferred embodiment of the invention, the explosive composition will comprise at least about 6% of nitroglycerine.
The solid fuel may be any one or more of a wide variety of materials. for example, wood pulp, bagasse, ivory nut "meal, ground walnut shells, apricot pit pulp, a flour such as corn flour, charcoal, coal, sulphur, and the like, and usually the solid fuel will be present in an amount between about 4% and about 15%.
In addition to the sensitizing agent and the solid fuel, ammonia dynamites usually, or at times, contain other materials, for example, nitro cotton, sodium nitrate, and an antacid such as calcium carbonate (chalk), magnesium carbonate, or the like. Any or all of these materials as well as other ingredients may be present in the explosive composition of the invention in proportions to provide an explosive of the desired characteristics, all as is well known in the art.
The reaction product employed will be sufiicient to provide the desired water-resistance and usually will be present in an amount between about and about 5%, preferably between about 1 and about 3%, based on the total weight of the 6 explosive composition, although amounts in excess of these figures and over that required for water-resistance may be employed without disadvantageous efiects.
The invention will be further described by means of the following specific examples:
Ammonium nitrate explosive compositions were prepared by conventional procedures to each of the formulae listed in the tables hereinafter set forth in which were incorporated, in accordance with the present invention, a reaction product of the type and in the amount specified in said tables.
Each of these explosive compositions were packed in conventional $4 x 8" paper cartridges. The ends of the cartridges were sealed with tallow. The wrapper of each of the cartridges was perforated with sixteen 4" holes arranged in four lines parallel to the axis and equidistantly spaced around the cartridge, the holes in adjacent rows being staggered. .Each cartridge was placed in a vessel, was covered with sand, and water was poured into the vessel until it stood above the sand. The cartridge was then removed from the sand after a known number of hours. and its detonability with a No. 6 blasting cap was determined. The results are shown in the tables-D designating that the composition detonated after the stated number of hours; F" designating that the composition failed to detonate in the stated number of hours. The data set forth in the tables show that explosive compositions containing the reaction product possessed greatly increased water-resistance.
Table I N itroglycerinc, Percent 6.0 6.0 8. 0 6. 0 6. 0 6.0 Wax-coated Fine Ammonium Nitrate, Percent 48. 5 48. 5 45. 1 Wax-coated Coarse Ammonium N itrate, Percent 80. 4 81. 0 s0. 4 Coarse Sodium Nitrate, Percent- 33. 2 33. 2 32. 4 5.0 5.0 5.0 Chalk, Percent 0. 5 0. 5 0. 5 0. 5 (l. 5 0. 5 Fine Apricot Pi Pulp, Percent-. 7. 3 6. 3 2. 9 4. l 3. 5 3. 1 Wood Pulp, Percent. 0.5 0. 5 0.5 2.0 2.0 2.0 Ground Sulphur, Percent. 4. 0 4. 0 4. 0 Yellow Corn Flour, Percent 5. 3 2. 0 1. 0 Water-Soluble Urea-Formaldehyde Reaction Product D 1 D 1 3.0 -24 water'Reslstance F-l6 F468 F-l92 F-3 F-192 F-48 l Freshly prepared dimetbylolurea in crystalline form.
2 Uiormite CB 553-a water-soluble urea-formaldehyde adhesive in the form of a. dry powder and containing a room-temperature-setting.catalyst, sold by Resinous Products Chemical Company (Rohm and Haas Company).
Table II Nitroglycerine, Percent 8.0 8.0 11.85 11.85 11.85 9.8 9.8 Nitro cotton, Percent 0. 05 0. 05 0. 05 Wax-coated Coarse Ammonium Nitrate, Percent 22.4 22.4 36.1 36.1
Wax-coated Fine Ammonium Nitrate,
Bagasse, Percent Fin Soft Coal, Percent Fine Apricot Pit Pulp, Percent.
W ater-Resistance 1 2. 0D 7 D-24 F-48 1 1. 00 2 D-lG F-24 l Cascamitea water-soluble urea-formaldehyde resin adhesive in the form of a dry powder, sold by Casein Company of America.
The water-resistance of this explosive compositioncontalnlng no urea-formaldehyde reaction product was: D-3; F-7.
Table III N itroglycerine, Percent; 11. 85 11. 85 11. 85 11. 85 11. 85 Nitro cotton, Percent 0. 05 0. 05 0.05 0. 05 0. 05 Wax-coated Fine Amm 39. 00 39. 00 39. 00 39. 00 39. 00 25. 00 25. 00 25. 0O 25. 00 25. 00 10. 60 10. 60 10. 60 10. 60 10. 60 3. O0 3. 00 3. 00 3.00 3. 00 Yellow Corn Flour, Percent. 4.00 5. 00 4. 00 5. 00 4.00 Ground Sulphur, Percent. 4. 00 4. 00 4. 00 4. 00 4.00 Chalk, Percent... 0.50 0.50 0.50 0.50 0.50 Partially Polymerized Water-Soluble Urea-F ormaldehyde Resin, Percent. 1 32.123 131.122 1 32.1 1 31.1 3 0g 1 -9 watel'Reslsmnw F-192 F-l68 F-192 F-168 F-l2Q Uformite 505a water-soluble urea-formaldehyde adhesive in the form of a dry powder and containing no catalyst sold by Resinous Products and Chemical Company (Rohm and Haas Company).
2 Uformite CD '553a Water-soluble urea-formaldehyde adhesive in the form of a dry powder and containing av room-temperature setting catalyst, sold by Resinous Products and Chemical Company (Rohm and Haas Company).
Plasl on Ready-Mixed 2502 G1uea water-soluble urea formaldehyde adhesive in the form of a. dry powder and containing a catalyst, sold by the Plaskon Division of Libbey-Owens-Ford Glass Company.
* ComparewitliNo. 3iof Table II;
Table IV Nitroglyccrinc, Percent 11. 85 11.85 11.85 6.0 6. 0 10.0 10.0 6.0 6.0 Nitrocotton, Percent; 0. 05' 0.05 0.05 Wax-coated Fine Ammonium Nitratc, Percent 39.00 39. 00 39. 00 48. 5 48. 5 42.0 42.0 Wax-coated Coarse Ammonium Nitrate, Percent 29. 5 29.5 30. 4 80.41 Coarse Sodium Nitrate, Percent 25.0 25.0 25. 0 33. 2 33. 2 8.0 8.0 5. 0 5. 0 Fine Sodium Nitrate, Percent 10. 6 6 1 6 Fine Apricot Pit Pulp, Percen 8.0 .0 .0 .1 Yellow Corn Flour, PercenL. 5.0 .0 0 Ground Sulphur, Percent.-- 4.0 .0 4.0 Wood Pulp, Percent 0. 5 0.5 2.0 2.0 Chalk, Percent 0.5 0.5 0. 5 0.5 0. 5 0.5 0.5 0.5 0, 5 Partially Polymerized, Water-so ublc Mclamine-Urea-Formaldehyde Resin, Percent 3 3 D a 31. 0 1 31. 0 1 1.0 1 1.0 1 1.0 1.0
Water Reslsmme u r-192 F-l92 F-i92 F32 F-48 r-m F-72 1x32 F4 1 A melamineurea-formaldehyde co-reacted resin containing approximately 18% inert filler material of a mixture of wood flour and walnut shell flour, sold byAmericanCyanamidand Chemical Corp. under the designation Melurac 300." Z A melamine-urea-formnldehyde co-reacted resin containing no filler, sold by American Cyanamid and Chemical Corp. under the designation Melura'c 301.
3 Compare with N0. 3 of Table II 4 Compare with No. 1 of Table I.
5 The water-resistance of this explosive composition containing no reaction product was: D-3; F-7.
Compare with No. 4 of Table I..
Table V Nitroglycerine, Percent 6.0 6.0 8.0 8.0 9. 8 9.8 Wax-coated Fine Ammonium Nitrate,
Percent 48. 5 48.5 45. 7 45. 7 36. l 36. 1
Bagasse, Percent .1 7. 0 Water-Soluble Melamine-Formaldehyde Reaction Product, Percent 4 1 1.0 4 2. 0 5 1 l. 0 3 1.0 2 2. 0 water-Resist nc are }??33 e3; at; as
1 Melmac S77W a water-soluble melamine-formaldehyde reaction product in the form of a dry powder and containing no filler and :only a small amount, if any, of catalyst, sold by American Cyanamid and Chemical Corp.
Melmac 401f a water-soluble melamine-formaldehyde reaction product in the form of a dry powder and containing; no filler and a very small amount, if any, of catalyst, sold by American Cyanamid and Chemical Corp.
Melmac 40 a :water-soluble melamine-formaldehyde reaction product in the form of a dry powder and containing no filler and a very small amount, if any, of catalyst, sold by American Cyanamid and Chemical Corp.
4 The water-resistance of this explosive composition containing no reaction product was: D-7;
5 The water-resistance of. this explosive composition containing no reaction product was: D-7;
The water-resistance 01: this explosive compositioncontoining no reaction product was: D-3;
Considerable modification is possible in the selection of the particular reaction product and the proportions thereof employed, a well as in other ingredients of the explosive composition, without departing from the present invention.
I claim:
1. The method of improving the water-resistance of an explosive composition comprising a mixture of granular ammonium nitrate, a sensitizer and a solid fuel which comprises intimately mixing with and substantially uniformly distributing throughout said mixture of granular ammonium nitrate, sensitizer and solid fuel, a solid, finely-divided hydrophilic reaction product of formaldehyde and at least one of the amino compounds selected from the group consisting of urea, thio'urea and melamine.
2. The method of claim 1 wherein said reaction product is a water-soluble partially polymerized urea-formaldehyde resin and is in an amount between about 0.5% and about 5% based on the weight of the explosive composition.
3. The method of claim 1 wherein said reaction product is a water-soluble partially polymerized melamine-formaldehyde resin and is in an amount between about 0.5% and about 5% based on the weight of the explosive composition.
4. The method of claim 1 wherein said reaction product is a water-soluble partially polymerized urea-melamine-formaldehyde resin and is in an amount between about 0.5% and about 5% based on the weight of the explosive composition.
5. The method of claim 1 wherein the said granular ammonium nitrate has a wax coating.
6. The method of improving the water-resistance of an explosive composition comprising a mixture of granular ammonium nitrate, at least one sensitizer selected from the group consisting of an explosive liquid nitric ester and a nitro aromatic compound, and a solid carbonaceous fuel which comprises intimately mixing with and substantially uniformly distributing throughout said mixture of granular ammonium nitrate, sensitizer and solid fuel, a solid, finely-divided hydrophilic reaction product of formaldehyde and at least one of the amino compounds selected from the group consisting of urea, thiourea and melamine.
7. The method of claim 6 wherein the sensitizer is nitroglycerin and is in an amount between about 6% and about 20% based on the weight of the explosive composition; and wherein said reaction product is a water-soluble partially polymerized urea-formaldehyde resin in an amount between about 0.5% and about 5% based on the weight of the explosive composition.
8. The method of claim 6 wherein the sensitizer is nitroglycerin and is in an amount between about 6% and about 20% based on the weight of the explosive composition; and wherein the reaction product is a water-soluble partially polymerized melamine-formaldehyde resin in an amount between about 0.5% and about 5% based on the Weight of the explosive composition.
9. The method of claim 6 wherein said granular ammonium nitrate has a wax coating.
WILLIAM C. LYTLE.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 2,327,968 Ripper Aug. 24, 1943 2,334,149 Ripper Nov. 9, 1943 FOREIGN PATENTS Number Country Date 579,057 Great Britain July 22, 1946

Claims (1)

1. THE METHOD OF IMPROVING THE WATER-RESISTANCE OF AN EXPLOSIVE COMPOSITION COMPRISING A MIXTURE OF GRANULAR AMMONIUM NITRATE, A SENSITIZER AND A SOLID FUEL WHICH COMPRISES INTIMATELY MIXING WITH AND SUBSTANTIALLY UNIFORMLY DISTRIBUTING THROUGHOUT SAID MIXTURE OF GRANULAR AMMONIUM NITRATE, SENSITIZER AND SOLID FUEL, A SOLID, FINELY-DIVIDED HYDROPHLIC REACTION PRODUCT OF FORMALDEHYDE AND AT LEAST ONE OF THE AMINO COMPOUNDS SELECTED FROM THE GROUP CONSISTING OF UREA, THIOUREA AND MELAMINE.
US121457A 1949-10-14 1949-10-14 Method of improving the waterresistance of ammonium nitrate explosives Expired - Lifetime US2630379A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US121457A US2630379A (en) 1949-10-14 1949-10-14 Method of improving the waterresistance of ammonium nitrate explosives
GB24706/50A GB674517A (en) 1949-10-14 1950-10-10 Improvements in or relating to ammonium nitrate containing explosive compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US121457A US2630379A (en) 1949-10-14 1949-10-14 Method of improving the waterresistance of ammonium nitrate explosives

Publications (1)

Publication Number Publication Date
US2630379A true US2630379A (en) 1953-03-03

Family

ID=22396862

Family Applications (1)

Application Number Title Priority Date Filing Date
US121457A Expired - Lifetime US2630379A (en) 1949-10-14 1949-10-14 Method of improving the waterresistance of ammonium nitrate explosives

Country Status (2)

Country Link
US (1) US2630379A (en)
GB (1) GB674517A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2841481A (en) * 1954-03-11 1958-07-01 Brock S Crystal Palace Firewor Pyrotechnic masses
US3053707A (en) * 1957-06-11 1962-09-11 Du Pont Blasting agent
US3160536A (en) * 1958-01-13 1964-12-08 Union Carbide Corp Blasting explosive
US3278350A (en) * 1963-02-11 1966-10-11 Ici Ltd Explosive-ammonium nitrate in phenol-aldehyde resin

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2327968A (en) * 1941-01-28 1943-08-24 American Cyanamid Co Porous xerogel
US2334149A (en) * 1938-02-18 1943-11-09 American Cyanamid Co Explosive
GB579057A (en) * 1943-07-03 1946-07-22 Charles A Thomas Improvements in or relating to propellant compositions suitable for projectiles of the reaction-impulse type

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2334149A (en) * 1938-02-18 1943-11-09 American Cyanamid Co Explosive
US2327968A (en) * 1941-01-28 1943-08-24 American Cyanamid Co Porous xerogel
GB579057A (en) * 1943-07-03 1946-07-22 Charles A Thomas Improvements in or relating to propellant compositions suitable for projectiles of the reaction-impulse type

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2841481A (en) * 1954-03-11 1958-07-01 Brock S Crystal Palace Firewor Pyrotechnic masses
US3053707A (en) * 1957-06-11 1962-09-11 Du Pont Blasting agent
US3160536A (en) * 1958-01-13 1964-12-08 Union Carbide Corp Blasting explosive
US3278350A (en) * 1963-02-11 1966-10-11 Ici Ltd Explosive-ammonium nitrate in phenol-aldehyde resin

Also Published As

Publication number Publication date
GB674517A (en) 1952-06-25

Similar Documents

Publication Publication Date Title
US3097120A (en) Gelled ammonium nitrate explosive containing polyacrylamide and an inorganic cross-linking agent
US3097121A (en) Powdered ammonium nitrate explosive containing polyacrylamide and an inorganic cross-linking agent
US2630379A (en) Method of improving the waterresistance of ammonium nitrate explosives
US3925122A (en) Molded explosive bodies having variable detonation speeds
US3507718A (en) Explosive slurry containing pulpy fibrous matter,finely divided carbonaceous material and powerful inorganic oxidizer salt
US4875950A (en) Explosive composition
US2334149A (en) Explosive
US3047441A (en) Hydrogen peroxide explosives
US3753810A (en) Nh{11 no{11 -nitrocellulose coated with nitrocellulose and al
US4637848A (en) High density gel explosive
US1932050A (en) Explosive coating material
US3026221A (en) Explosive composition
US3160535A (en) Free flowing granular explosive composition of controlled particle size
US2433417A (en) Blasting explosive
US3144367A (en) Inorganic nitrate explosive composition coated with hydrazine or guanidine compounds
US2654666A (en) Explosive
US2537039A (en) Gelatinous explosive composition
US2674526A (en) Gelatin dynamite composition containing sulfur
US2759807A (en) Gelatinous explosive compositions
US3328217A (en) Aqueous blasting compositions containining particulate smokeless powder and dinitrotoluene
NO153096B (en) GELATINED EXPLOSION
US2055403A (en) Explosive
US3668027A (en) Method of making nitrocellulose-nitroglycerine water-bearing explosive compositions
US1658816A (en) Casl d
US2344840A (en) Explosive composition and method of producing same