US2821466A - Nitrate explosives and method of making - Google Patents

Nitrate explosives and method of making Download PDF

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Publication number
US2821466A
US2821466A US478183A US47818354A US2821466A US 2821466 A US2821466 A US 2821466A US 478183 A US478183 A US 478183A US 47818354 A US47818354 A US 47818354A US 2821466 A US2821466 A US 2821466A
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Prior art keywords
nitrostarch
trinitrate
inorganic
trimethylolethane
granules
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US478183A
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Edward J Russell
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Trojan Powder Co
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Trojan Powder Co
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    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B45/00Compositions or products which are defined by structure or arrangement of component of product
    • C06B45/18Compositions or products which are defined by structure or arrangement of component of product comprising a coated component
    • C06B45/30Compositions or products which are defined by structure or arrangement of component of product comprising a coated component the component base containing an inorganic explosive or an inorganic thermic component
    • C06B45/32Compositions or products which are defined by structure or arrangement of component of product comprising a coated component the component base containing an inorganic explosive or an inorganic thermic component the coating containing an organic compound
    • C06B45/34Compositions 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 the compound being an organic explosive or an organic thermic component

Definitions

  • This invention relates to blasting explosives of the type designated as dynamites, manufactured with compositions containing mixtures of trimethylolethane trinitrate and nitrostarch.
  • nitroglycerin In the manufacture of dynamites it is customary to employ nitroglycerin with or without the addition of nitropolyglycerin, nitrated sugars, ethyleneglycol dinitrate and similar explosives soluble in nitroglycerin in conjunction with nitrocellulose which is colloidally dispersed by the nitroglycerin and to some extent by the nitropolyglycerin, nitrated sugars, ethyleneglycol dinitrate, etc.
  • trimethylolethane trinitrate has no such colloiding action on nitrocellulose at ordinary temperatures, it being necessary to heat mixtures of trimethylolethane trinitrate and nitrocellulose to approximately 80 C. before colloidal dispersion of the nitrocellulose is effected. This renders trimethylolethane trinitrate alone unsuitable for use as a colloiding agent for nitrocellulose in dynamite manufacture.
  • Nitrostarch is chemically identical with nitrocellulose, the two materials differing physically in that nitrocellulose is fibrous in structure while nitrostarch consists of granules and the molecule of nitrocellulose is of greater size than that of nitrostarch. It would therefore be anticipated that the colloiding action of trimethylolethane trinitrate on nitrostarch would be similar to that of its action on nitrocellulose.
  • nitrostarch is much less expensive than nitrocellulose and has other advantageous characteristics in manufacture and use as compared with nitrocellulose, and because trimethylolethane trinitrate has a lower freezing point than nitroglycerin and is more stable and viscous and less sensitive and volatile than nitroglycerin, the use of these materials together in the manufacture of dynamites would be very desirable.
  • trimethylolethane trinitrate has significant and valuable colloiding action on nitrostarch at ordinary temperatures and that heating of the mixture is not necessary as in the case of mixtures of trimethylolethane trinitrate and nitrocellulose.
  • nitro starch containing 13.0 percent nitrogen are mixed at ordinary temperatures with 100 parts by weight of trimethylolethane trinitrate, it is found that the liquid trinitrate dissolves-i. e., colloidally dispersesapproximately 1.5 parts by weight of the nitrostarch.
  • the undissolved granules of nitrostarch have become swollen in size and are soft and jelly-like in consistency. If nitrostarch containing less than 13.0 percent nitrogen is so used, even more of the material is dissolved and the undissolved material is even more swollen in size and softer.
  • a coating of such a colloidal dispersion of nitrostarch in trimethylolethane trinitrate is highly efiective in water-proofing such water-soluble inorganic salts as ammonium nitrate and sodium nitrate. If there is present in the mixture more nitrostarch than the trimethylolethane trinitrate can dissolve, the swollen, undissolved granules of nitrostarch serve to enhance the adhesive and moisture-proofing effects of the solution of nitrostarch in TMETN.
  • the particular mixture of trimethylolethane trinitrate and nitrostarch that I may use in a dynamite composition depends upon the other ingredients to be used, the explosive power and sensitivity desired and the requirement with respect to water resistance.
  • the dynamite composi tions manufactured with these two ingredients may contain 5 to 49 percent trimethylolethane trinitrate and 0.5 to 30 percent nitrostarch.
  • compositions containing trimethylolethane trinitrate and nitrostarch the following are mentioned:
  • the inorganic nitrates that I prefer to use are the nitrates of ammonia, sodium and potassium, and the particle size which I prefer is material all of which will pass through a sieve having ten meshes to the linear inch, and of which less than 50% will pass through a sieve having meshes to the linear inch.
  • the process whih comprises stirring 47.5-84.5 parts by weight of granules of an-inorganic nitrateselected from-the group consisting -of ammonium, sodium and potassium nitrates :and mixtures thereofwith a viscous mixture of0.5- 30 "parts of nitrostarch and S-40 -parts of trimethylolethane '4' trinitrate in which some at least of the nitrostarch is in the form of a colloidal solution in the "said trinitrate, the said solution being in proportion to coat the inorganic nitrate granules, and continuing the stirring until the coating of the granules is efiected.

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  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Organic Chemistry (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

United States Patent NITRATE EXPLOSIVES AND METHOD OF MAKING Edward J. Russell, South Whitehall Township, Lehigh County, Pa., assignor to Trojan Powder Company, a
corporation of New York No Drawing. Application December 28, 1954 Serial No. 478,183
3 Claims. (Cl. 52-11) This invention relates to blasting explosives of the type designated as dynamites, manufactured with compositions containing mixtures of trimethylolethane trinitrate and nitrostarch.
In the manufacture of dynamites it is customary to employ nitroglycerin with or without the addition of nitropolyglycerin, nitrated sugars, ethyleneglycol dinitrate and similar explosives soluble in nitroglycerin in conjunction with nitrocellulose which is colloidally dispersed by the nitroglycerin and to some extent by the nitropolyglycerin, nitrated sugars, ethyleneglycol dinitrate, etc. It is well known that trimethylolethane trinitrate has no such colloiding action on nitrocellulose at ordinary temperatures, it being necessary to heat mixtures of trimethylolethane trinitrate and nitrocellulose to approximately 80 C. before colloidal dispersion of the nitrocellulose is effected. This renders trimethylolethane trinitrate alone unsuitable for use as a colloiding agent for nitrocellulose in dynamite manufacture.
Nitrostarch is chemically identical with nitrocellulose, the two materials differing physically in that nitrocellulose is fibrous in structure while nitrostarch consists of granules and the molecule of nitrocellulose is of greater size than that of nitrostarch. It would therefore be anticipated that the colloiding action of trimethylolethane trinitrate on nitrostarch would be similar to that of its action on nitrocellulose.
Because nitrostarch is much less expensive than nitrocellulose and has other advantageous characteristics in manufacture and use as compared with nitrocellulose, and because trimethylolethane trinitrate has a lower freezing point than nitroglycerin and is more stable and viscous and less sensitive and volatile than nitroglycerin, the use of these materials together in the manufacture of dynamites would be very desirable.
It has been found that, contrary to expectation, trimethylolethane trinitrate has significant and valuable colloiding action on nitrostarch at ordinary temperatures and that heating of the mixture is not necessary as in the case of mixtures of trimethylolethane trinitrate and nitrocellulose. If five or more parts by weight of nitro starch containing 13.0 percent nitrogen are mixed at ordinary temperatures with 100 parts by weight of trimethylolethane trinitrate, it is found that the liquid trinitrate dissolves-i. e., colloidally dispersesapproximately 1.5 parts by weight of the nitrostarch. Furthermore, it is found that the undissolved granules of nitrostarch have become swollen in size and are soft and jelly-like in consistency. If nitrostarch containing less than 13.0 percent nitrogen is so used, even more of the material is dissolved and the undissolved material is even more swollen in size and softer.
Because of the high viscosity of trimethylolethane trinitrate as compared with nitroglycerin (156 and 35.5 centipoises at 20 C. respectively), such a colloidal dispersion of nitrostarch in trimethylolethane trinitrate is extremely sticky or adhesive and therefore serves as a superior coating and sensitizing agent for insensitive inorganic salts such as the ammonium nitrate and sodium nitrate commonly used in dynamite compositions. Because of the practical insolubility of trimethylolethane trinitrate in water (less than 0.01 gram per grams of water at 25 C. as compared with 0.14 gram for nitroglycerin), a coating of such a colloidal dispersion of nitrostarch in trimethylolethane trinitrate is highly efiective in water-proofing such water-soluble inorganic salts as ammonium nitrate and sodium nitrate. If there is present in the mixture more nitrostarch than the trimethylolethane trinitrate can dissolve, the swollen, undissolved granules of nitrostarch serve to enhance the adhesive and moisture-proofing effects of the solution of nitrostarch in TMETN.
The particular mixture of trimethylolethane trinitrate and nitrostarch that I may use in a dynamite composition depends upon the other ingredients to be used, the explosive power and sensitivity desired and the requirement with respect to water resistance. The dynamite composi tions manufactured with these two ingredients may contain 5 to 49 percent trimethylolethane trinitrate and 0.5 to 30 percent nitrostarch.
As examples of preferred compositions containing trimethylolethane trinitrate and nitrostarch, the following are mentioned:
acids as calcium carbonate, zinc oxide, magnesium oxide or mixtures of two or more of these. It is to be noted that my claim of invention is not restricted to compositions containing only the ingredients shown in the above examples, as I may use substitutes for these ingredients other than trimethylolethane trinitrate and nitrostarch and add ingredients such as TNT, liquid nitrotoluenes, sodium chloride, ammonium chloride, alum, ammonium sulphate or gypsum.
Although I do not wish to limit myself to the use of any particular inorganic nitrate, or mixture of inorganic nitrates or to the use of such inorganic nitrates in particles of any specific size, the inorganic nitrates that I prefer to use are the nitrates of ammonia, sodium and potassium, and the particle size which I prefer is material all of which will pass through a sieve having ten meshes to the linear inch, and of which less than 50% will pass through a sieve having meshes to the linear inch. This represents the particle size of the inorganic nitrates most generally used in the formulation of dynamites of the customary type containing nitroglycerin as the sensitizing ingredient.
It is to be understood that it is intended to cover all changes and modifications of the examples of the invention herein chosen for the purpose of the illustration which do not constitute departures from the spirit and scope of the invention.
I claim:
1. A detonatable explosive composition consisting essentially of granules of an inorganic nitrate selected from the group consisting of ammonium, sodium and potassium nitrates and mixtures thereof, trimethylolethane "trinitrate "and-'nitros'tarch, "the nitrostarch being at least in part in the form of *a 'colloidal =solution"in"the*said trinitrate, the said solution coating the granules of the inorganic nitrate and providing sensitizing and Waterproofing therefor, "and *the proportions "by weight being about 475-845 parts of the inorganic nitrate, "5-40 of "the said trinitrate and 0.5 30 of the nitrostareh.
'2. "The 'explosive of *Claim 1 in which some 'at least of the =n'itrostarch'is suspended innon-colloidal form in said colloidal solution.
3.11m 'making a -detonatable explosive, the process whih comprises stirring 47.5-84.5 parts by weight of granules of an-inorganic nitrateselected from-the group consisting -of ammonium, sodium and potassium nitrates :and mixtures thereofwith a viscous mixture of0.5- 30 "parts of nitrostarch and S-40 -parts of trimethylolethane '4' trinitrate in which some at least of the nitrostarch is in the form of a colloidal solution in the "said trinitrate, the said solution being in proportion to coat the inorganic nitrate granules, and continuing the stirring until the coating of the granules is efiected.
References Cited in the file of this patent UNITED f-STATES PATENTS 1,728,307 Rupp ..1Sep. 17, 1929 1,883,044 Spaeth Oct. 18, 1932 1,932,050 Spaeth Oct. '24, 1933 2,171,379 Wahl -n Augn29, 1939 FOREIGN PATENTS 442,850 Great'Britain Nov. 14, 1934

Claims (1)

1. A DETONABLE EXPLOSIVE COMPOSITION CONSISTING ESSENTIALLY OF GRANULES OF AN INORGANIC NITRATES SELECTED FROM THE GROUP CONSITING OF AMMONIUM, SODIUM AND POTASSIUM NITRATES AND MIXTURES THEREOF, TRIMETHYLOLETHANE TRINITTRATE AND NITROSTARCH, THE NITROSTARCH BEING AT LEAST IN PART IN THE FORM OF A COLLOIDAL SOLUTION IN THE SAID TRINITRATE, THE SAID SOLUTION COATING THE GRANULES OF THE INORGANIC NITRATE AND PROVIDING SENSITIZING AND WATERPROOFING THEREFOR, AND THE PROPORTIONS BY WEIGHT BEING ABOUT 47.5-84.5 PARTS OF THE INORGANIC NITRATE, 5-40 OF THE SAID TRINIRATE AND 0.5-30 OF THE NITROSTARCH.
US478183A 1954-12-28 1954-12-28 Nitrate explosives and method of making Expired - Lifetime US2821466A (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3344005A (en) * 1966-02-23 1967-09-26 Trojan Powder Co Pentaerythritol tetranitrate-trimethylolethane trinitrate explosives
WO1999044968A1 (en) * 1998-03-06 1999-09-10 Snc Industrial Technologies Inc. / Les Technologies Industrielles Snc Inc. Non-toxic primers for small caliber ammunition

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1728307A (en) * 1928-02-29 1929-09-17 Trojan Powder Co Explosive
US1883044A (en) * 1931-11-20 1932-10-18 Du Pont Explosive composition
US1932050A (en) * 1933-10-24 Explosive coating material
GB442850A (en) * 1934-05-14 1936-02-17 Bombrini Parodi Delfino Improvements in and relating to the production of explosives
US2171379A (en) * 1938-09-28 1939-08-29 Du Pont Ammonium nitrate explosive

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1932050A (en) * 1933-10-24 Explosive coating material
US1728307A (en) * 1928-02-29 1929-09-17 Trojan Powder Co Explosive
US1883044A (en) * 1931-11-20 1932-10-18 Du Pont Explosive composition
GB442850A (en) * 1934-05-14 1936-02-17 Bombrini Parodi Delfino Improvements in and relating to the production of explosives
US2171379A (en) * 1938-09-28 1939-08-29 Du Pont Ammonium nitrate explosive

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3344005A (en) * 1966-02-23 1967-09-26 Trojan Powder Co Pentaerythritol tetranitrate-trimethylolethane trinitrate explosives
WO1999044968A1 (en) * 1998-03-06 1999-09-10 Snc Industrial Technologies Inc. / Les Technologies Industrielles Snc Inc. Non-toxic primers for small caliber ammunition

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