US3138496A - Granular cyclotrimethylenetrinitramine explosive coated with alkyl amide and microcrystalline wax - Google Patents
Granular cyclotrimethylenetrinitramine explosive coated with alkyl amide and microcrystalline wax Download PDFInfo
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- US3138496A US3138496A US116665A US11666561A US3138496A US 3138496 A US3138496 A US 3138496A US 116665 A US116665 A US 116665A US 11666561 A US11666561 A US 11666561A US 3138496 A US3138496 A US 3138496A
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- Prior art keywords
- cyclonite
- wax
- microcrystalline wax
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- explosive
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- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B25/00—Compositions containing a nitrated organic compound
- C06B25/34—Compositions containing a nitrated organic compound the compound being a nitrated acyclic, alicyclic or heterocyclic amine
-
- C—CHEMISTRY; METALLURGY
- C06—EXPLOSIVES; MATCHES
- C06B—EXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
- C06B45/00—Compositions or products which are defined by structure or arrangement of component of product
- C06B45/18—Compositions or products which are defined by structure or arrangement of component of product comprising a coated component
- C06B45/20—Compositions or products which are defined by structure or arrangement of component of product comprising a coated component the component base containing an organic explosive or an organic thermic component
- C06B45/22—Compositions or products which are defined by structure or arrangement of component of product comprising a coated component the component base containing an organic explosive or an organic thermic component the coating containing an organic compound
Definitions
- This invention relates to explosives compositions and more particularly to such compositions containing desensitized cyclonite.
- Cyclotrimethylenetrinitramine which is frequently called cyclonite, is a commercially attractive explosive since it is exceedingly powerful, relatively non-toxic, and waterproof. Because of its great strength, it is used extensively in seismic exploration operations, in blasting, and in all applications requiring a high brisant explosive. This explosive compound is relatively insensitive in comparison with nitroglycerin compositions. However, pure dry cyclonite is too sensitive to permit shipping in interstate commerce. In order to pass the regulations of the Interstate Commerce Commission, this material must be sufficiently insensitive that it will not detonate when an 8 pound weight is dropped on it from a height of 7 inches.
- cyclonite for commercial shipping involves coating with 4 percent or 5 percent of a microcrystalline wax which desensitizes it sufficiently to comply with I.C.C. regulations. Although such wax coatings are generally satisfactory, they materially reduce the amount of explosive per pound of desensitized material. Thus, when a given weight of cyclonite is needed, the handling and shipping of inordinately large quantities of desensitizing material is involved. Also, the force of the explosive charge is necessarily diluted by the presence of the inert coating material.
- an object of this invention to provide new and novel desensitized cyclonite compositions and a method of preparing the same. Another object of this invention is to provide desensitized explosive compositions having maximum power. Another object of this invention is to provide cyclonite desensitized with a minimum of non-explosive material.
- Suitable amides and amines include prelargonamide, capramide, myristamide, palmitamide, stearamide, octylamine, nonylamine, dodecylamine, tetradecylamine, octadecylamine, etc. and mixtures thereof.
- this invention contemplates cyclonite desensitized with between about 0.8 percent and about 2.5 percent of a mixture of a microcrystalline wax and an alkyl amide or amine with the organic base representing at least 0.65 percent of the weight of the cyclonite.
- Compositions containing less than about 0.65 percent of the organic base are not reliably desensitized.
- cyclonite coated with less than about 0.8 percent of the wax-base mixture is inadequately desensitized. Amounts of the coating mixture in excess of 2.5 percent do not enhance the properties of the explosive but merely act as a diluent.
- microcrystalline wax having a melting point in excess of about 75 C. can be used in accordance with the present invention.
- Suitable microcrystalline waxes include tank bottom microcrystalline wax, motor oil wax, residual microcrystalline wax, and the like, as well as mixtures thereof. Any of the various microcrystalline waxes can be obtained by processes well known to the art.
- Cyclonite can be coated with the wax-organic base mixture in any conventional manner.
- the dry material can be tumbled consecutively with each component of the mixture until a uniform coating is obtained.
- the material to be desensitized can be tumbled with a premixture of the coating ingredients. It is preferred, however, to suspend the explosive material in an aqueous slurry which is heated prior to the addition of the coating mixture.
- the cyclonite is then mixed with the coating mixture above its melting point until a substantially uniform coating is obtained. At this point, the water is removed by filtration, decantation, or by any other suitable method and the product is: dried.
- a major problem experienced previously with all explosive materials desensitized with a parafiin wax has been that of migration of the wax from the crystal surface of the explosive material when the explosive compositions are subjected to elevated temperatures such as encountered in oil well perforation operations.
- cyclonite is exploded with an initiator charge.
- the wax employed to desensitize the cyclonite migrates into the initiator charge at the high temperatures encountered in deep wells the result is that the initiator itself is desensitized to such an extent that it may not fire.
- Such coatings have high melting points, they are flexible even at low temperatures, they possess excellent adhesive as well as good cohesive properties, and, in addition, they are pliable.
- Paraffin wax cannot be utilized in place of microcrystalline wax to prepare the valuable products of this invention because the films formed with it and the alkyl amine or amide are low melting, brittle and they exhibit a lack of adhesion.
- the wax and the organic amide were readily compatible and formed a mixture with a melting point from about 93 C. to 95 C.
- the temperature of the slurry was elevated to about 97 C., slightly above the melting point of the coating material.
- the agitated slurry was maintained at this temperature for about 15 minutes and then cooled to about 65 C. by running cold water through the jacket of the vessel. When the suspension was thus cooled, it was removed from the vessel'andpoured over a filter bed to remove the water from the coated cyclonite. The resultant product was then dried at 75 C. for 48 hours to obtain a material having a moisturecontent less than 0.1 percent.
- the sensitivity of the cyclonite treated in this manner was determined by the Bureau of Explosives Impact Apparatus Test. In accordance with this test, an 8 pound steel ball is dropped on a compressed pellet of the explosive .003 of an inch thick and .2 of an inch in diameter confined rigidly between hard steel surfaces. In carrying out this test, 10 samples are subjected to the impact of an 8 pound ball dropping from a height of 7 inches. If any one of the samples detonates, the material cannot be shipped in interstate commerce.
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Description
United States Patent 3,138,496 GRANULAR CYCLO'IRIMETHYLENETRINITRA- MINE EXPLOSIVE COATED WITH ALKYL AMIDE AND WCROCRYSTALLINE WAX Forrest V. Monica], Alton, 111., assignor, by mesne assignments, to Commercial Solvents Corporation, a corporation of Maryland No Drawing. Filed June 13, 1961, Ser. No.116,665 2 Claims. (Cl. 149-11) This application is a continuation-in-part of copending application Serial Number 843,915, now abandoned, filed October 2, 1959.
This invention relates to explosives compositions and more particularly to such compositions containing desensitized cyclonite.
Cyclotrimethylenetrinitramine, which is frequently called cyclonite, is a commercially attractive explosive since it is exceedingly powerful, relatively non-toxic, and waterproof. Because of its great strength, it is used extensively in seismic exploration operations, in blasting, and in all applications requiring a high brisant explosive. This explosive compound is relatively insensitive in comparison with nitroglycerin compositions. However, pure dry cyclonite is too sensitive to permit shipping in interstate commerce. In order to pass the regulations of the Interstate Commerce Commission, this material must be sufficiently insensitive that it will not detonate when an 8 pound weight is dropped on it from a height of 7 inches.
The customary preparation of cyclonite for commercial shipping involves coating with 4 percent or 5 percent of a microcrystalline wax which desensitizes it sufficiently to comply with I.C.C. regulations. Although such wax coatings are generally satisfactory, they materially reduce the amount of explosive per pound of desensitized material. Thus, when a given weight of cyclonite is needed, the handling and shipping of inordinately large quantities of desensitizing material is involved. Also, the force of the explosive charge is necessarily diluted by the presence of the inert coating material.
It is, therefore, an object of this invention to provide new and novel desensitized cyclonite compositions and a method of preparing the same. Another object of this invention is to provide desensitized explosive compositions having maximum power. Another object of this invention is to provide cyclonite desensitized with a minimum of non-explosive material.
In accordance with this invention, these and other objects are accomplished, generally speaking, by providing granular cyclonite with a coating of a mixture of a microcrystalline wax and long chain fatty acid amide or amine. The basic amide or amine is an alkyl amide or amine containing between 8 and 20 carbon atoms in the alkyl chain. Suitable amides and amines include prelargonamide, capramide, myristamide, palmitamide, stearamide, octylamine, nonylamine, dodecylamine, tetradecylamine, octadecylamine, etc. and mixtures thereof. More specifically this invention contemplates cyclonite desensitized with between about 0.8 percent and about 2.5 percent of a mixture of a microcrystalline wax and an alkyl amide or amine with the organic base representing at least 0.65 percent of the weight of the cyclonite. Compositions containing less than about 0.65 percent of the organic base are not reliably desensitized. Likewise, cyclonite coated with less than about 0.8 percent of the wax-base mixture is inadequately desensitized. Amounts of the coating mixture in excess of 2.5 percent do not enhance the properties of the explosive but merely act as a diluent.
Any type of microcrystalline wax having a melting point in excess of about 75 C. can be used in accordance with the present invention. Suitable microcrystalline waxes include tank bottom microcrystalline wax, motor oil wax, residual microcrystalline wax, and the like, as well as mixtures thereof. Any of the various microcrystalline waxes can be obtained by processes well known to the art.
Cyclonite can be coated with the wax-organic base mixture in any conventional manner. Thus, the dry material can be tumbled consecutively with each component of the mixture until a uniform coating is obtained. Alternately, the material to be desensitized can be tumbled with a premixture of the coating ingredients. It is preferred, however, to suspend the explosive material in an aqueous slurry which is heated prior to the addition of the coating mixture. The cyclonite is then mixed with the coating mixture above its melting point until a substantially uniform coating is obtained. At this point, the water is removed by filtration, decantation, or by any other suitable method and the product is: dried.
A major problem experienced previously with all explosive materials desensitized with a parafiin wax has been that of migration of the wax from the crystal surface of the explosive material when the explosive compositions are subjected to elevated temperatures such as encountered in oil well perforation operations. In such operations cyclonite is exploded with an initiator charge. When the wax employed to desensitize the cyclonite migrates into the initiator charge at the high temperatures encountered in deep wells the result is that the initiator itself is desensitized to such an extent that it may not fire. It has been found that when cyclonite is coated with a mixture of a microcrystalline wax and an alkyl amine or amide containing between 8 to 20 carbon atoms in the alkyl chain as described herein the problem of wax migration is substantially decreased because of the high melting point of the wax-base mixture.
Microcrystalline wax and the alkyl amide or amine when melted together form a mixture which when applied to cyclonite in the manner described herein yields a coating with extremely desirable properties. Such coatings have high melting points, they are flexible even at low temperatures, they possess excellent adhesive as well as good cohesive properties, and, in addition, they are pliable. Paraffin wax cannot be utilized in place of microcrystalline wax to prepare the valuable products of this invention because the films formed with it and the alkyl amine or amide are low melting, brittle and they exhibit a lack of adhesion.
In order to clarify the invention and to more fully describe the method by which it is carried out to achieve its various objects, the following is a detailed description of a preferred embodiment thereof. In this embodiment and throughout the specification, all proportions are ex pressed in parts by weight.
About 500 parts of crystalline cyclonite having a granulation such that it will pass through a US. No. 10 screen and be retained on a US. No. 325 screen were introduced into a jacketed vessel containing approximately 2,000 parts of water. The cyclonite and water were agitated to form a uniform aqueous slurry. Agitation was continued throughout the process. The vessel was heated by steam in the jacket to about C. When this temperature was reached, about 4 parts of a fatty acid amide having an average carbon chain length of about 18 and a melting point of about 100 C. to 102 C. together with 1 part of microcrystalline wax were added to the aqueous suspension. The microcrystalline wax used was a highly refined paraflinic wax having a melting point of about 77 C. to 80 C. The wax and the organic amide were readily compatible and formed a mixture with a melting point from about 93 C. to 95 C. After the components of the coating composition were added to the vessel, the temperature of the slurry was elevated to about 97 C., slightly above the melting point of the coating material.
The agitated slurry was maintained at this temperature for about 15 minutes and then cooled to about 65 C. by running cold water through the jacket of the vessel. When the suspension was thus cooled, it was removed from the vessel'andpoured over a filter bed to remove the water from the coated cyclonite. The resultant product was then dried at 75 C. for 48 hours to obtain a material having a moisturecontent less than 0.1 percent. The sensitivity of the cyclonite treated in this manner was determined by the Bureau of Explosives Impact Apparatus Test. In accordance with this test, an 8 pound steel ball is dropped on a compressed pellet of the explosive .003 of an inch thick and .2 of an inch in diameter confined rigidly between hard steel surfaces. In carrying out this test, 10 samples are subjected to the impact of an 8 pound ball dropping from a height of 7 inches. If any one of the samples detonates, the material cannot be shipped in interstate commerce.
When subjected to this test, the desensitized cyclonite of the present invention did not detonate, whereas the same material coated with 2 percent microcrystalline wax alone failed consistently. The results of these tests on the product of the present invention and on cyclonite coated with Wax only is set forth in the following table:
7 Coating Fall in Inches 2 1 5 Pen cent cent Wax cent Wax Mixture Wax /10 O/lO 1/10 2/10 0/10 2/10 3/5 l/5 1/3 1/3 2/3 2/3 but none detonated. From the tabulated results, it is clear that cyclonite coated with 1 percent of the mixture of the present invention is more thoroughly desensitized than cyclonite coated with 2 percent wax. Also, it is self-evident that cyclonite thus coated has been desensitized to substantially the same degree as cyclonite coated with the conventional 5 percent Wax. Thus, in accord ance with this invention, cyclonite can be desensitized with a much smaller amount of coating material than have been heretofore found practical.
The above description is directed exclusively to cyclonite alone. It will be understood, however, that the cyclonite prepared in accordance with this invention can be mixed with other explosives and components in the preparation of commercial explosive compositions.
Although the invention has been described in considerable detail in the foregoing, it is to be understood that the purpose of such detail is only for clarification of the invention and that many modifications can be made by those skilled in the art Without departing from the spirit and scope of the invention except as it is limited by the appended claims.
What is claimed is:
1. Granular cyclotrimethylenetrinitramine coated with about 0.8 percent to about 2.5 percent of a mixture of a microcrystalline wax and an alkyl amide containing between 8 and 20 carbon atoms in each alkyl chain, said alkyl amide representing at least 0.65 percent of the weight of the cyclotrimethylenetrinitramine.
2. Granular cyclotrimethylenetrinitramine coated with about 1 percent of a mixture of a microcrystalline wax and an alkyl amide containing between 8 and 20 carbon atoms in each alkyl chain, the weight ratio of said alkyl amide to said microcrystalline wax being at least 4:1.
References Cited in the file of this patent UNITED STATES PATENTS 3,000,720 Baer et a1 Sept. 19, 1961 FOREIGN PATENTS 123,252 Australia Jan. 3, 1947 574,271 Great Britain Dec. 31, 1945
Claims (1)
1. GRANNULAR CYCLOTRIMETHYLENETRINITRAMINE COATED WITH ABOUT 0.8 PERCENT TO ABOUT 2.5 PERCENT OF A MIXTURE OF A MICROCRYSTALLINE WAX AND AN ALKYL AMIDE CONTAINING BETWEEN 8 AND 20 CARBON ATOMS IN ACH ALKYL CHAIN, SAID ALKYL AMIDE REPRESENTING AT LEAST 0.65 PERCENT OF THE WEIGHT OF THE CYCLOTRIMETHYLENETRINITRAMINE.
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US116665A US3138496A (en) | 1961-06-13 | 1961-06-13 | Granular cyclotrimethylenetrinitramine explosive coated with alkyl amide and microcrystalline wax |
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US116665A US3138496A (en) | 1961-06-13 | 1961-06-13 | Granular cyclotrimethylenetrinitramine explosive coated with alkyl amide and microcrystalline wax |
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Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3346429A (en) * | 1965-03-22 | 1967-10-10 | Union Oil Co | Ammonium nitrate, kaolin clay, monoamine mixture sensitized with liquid hydrocarbon and preparation |
US3466205A (en) * | 1965-03-01 | 1969-09-09 | Armees France | Explosive containing hexogene or octogene and a nitrated n-methylaniline |
US3507719A (en) * | 1959-11-02 | 1970-04-21 | Solid Fuels Corp | Extrudable solid propellant composition containing metallic fuel particles and oxidizer particles dispersed in a waxy binder |
US3544360A (en) * | 1968-04-18 | 1970-12-01 | Nat Defence Canada | Process for desensitizing solid explosive particles by coating with wax |
US4097317A (en) * | 1977-03-25 | 1978-06-27 | The United States Of America As Represented By The Secretary Of The Navy | Desensitizing agent for compositions containing crystalline high-energy nitrates or nitrites |
FR2390406A1 (en) * | 1977-05-11 | 1978-12-08 | United Kingdom Government | PROCESS FOR THE PREPARATION OF A DESENSITIZED EXPLOSIVE COMPOUND |
US4163681A (en) * | 1970-04-15 | 1979-08-07 | The United States Of America As Represented By The Secretary Of The Navy | Desensitized explosives and castable thermally stable high energy explosive compositions therefrom |
US4770728A (en) * | 1984-02-08 | 1988-09-13 | Dyno Industrier A.S. | Method for coating high energy explosive crystals |
US5238512A (en) * | 1987-06-04 | 1993-08-24 | Exploweld Ab | Water resistant elastic explosive mixture |
WO1997042138A1 (en) * | 1996-05-03 | 1997-11-13 | Eastman Chemical Company | Explosive formulations |
WO1997042137A1 (en) * | 1996-05-06 | 1997-11-13 | Eastman Chemical Company | Explosive formulations |
WO1997042140A1 (en) * | 1996-05-03 | 1997-11-13 | Eastman Chemical Company | Explosive formulations |
WO1998016485A1 (en) * | 1996-10-15 | 1998-04-23 | Eastman Chemical Company | Explosive formulations |
US5801326A (en) * | 1997-04-18 | 1998-09-01 | Eastman Chemical Company | Explosive formulations |
RU2451650C1 (en) * | 2010-12-20 | 2012-05-27 | Федеральное государственное унитарное предприятие "Научно-исследовательский институт полимерных материалов" | Method of octogene modification |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB574271A (en) * | 1942-09-09 | 1945-12-31 | Ernest Gordon Cockbain | Desensitization of explosives |
US3000720A (en) * | 1959-04-09 | 1961-09-19 | Baer Maurice | Desensitization of cyclotrimethylenetrinitramine with dinitroethylbenzene |
-
1961
- 1961-06-13 US US116665A patent/US3138496A/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB574271A (en) * | 1942-09-09 | 1945-12-31 | Ernest Gordon Cockbain | Desensitization of explosives |
US3000720A (en) * | 1959-04-09 | 1961-09-19 | Baer Maurice | Desensitization of cyclotrimethylenetrinitramine with dinitroethylbenzene |
Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3507719A (en) * | 1959-11-02 | 1970-04-21 | Solid Fuels Corp | Extrudable solid propellant composition containing metallic fuel particles and oxidizer particles dispersed in a waxy binder |
US3466205A (en) * | 1965-03-01 | 1969-09-09 | Armees France | Explosive containing hexogene or octogene and a nitrated n-methylaniline |
US3346429A (en) * | 1965-03-22 | 1967-10-10 | Union Oil Co | Ammonium nitrate, kaolin clay, monoamine mixture sensitized with liquid hydrocarbon and preparation |
US3544360A (en) * | 1968-04-18 | 1970-12-01 | Nat Defence Canada | Process for desensitizing solid explosive particles by coating with wax |
US4163681A (en) * | 1970-04-15 | 1979-08-07 | The United States Of America As Represented By The Secretary Of The Navy | Desensitized explosives and castable thermally stable high energy explosive compositions therefrom |
US4097317A (en) * | 1977-03-25 | 1978-06-27 | The United States Of America As Represented By The Secretary Of The Navy | Desensitizing agent for compositions containing crystalline high-energy nitrates or nitrites |
FR2390406A1 (en) * | 1977-05-11 | 1978-12-08 | United Kingdom Government | PROCESS FOR THE PREPARATION OF A DESENSITIZED EXPLOSIVE COMPOUND |
US4770728A (en) * | 1984-02-08 | 1988-09-13 | Dyno Industrier A.S. | Method for coating high energy explosive crystals |
US5238512A (en) * | 1987-06-04 | 1993-08-24 | Exploweld Ab | Water resistant elastic explosive mixture |
WO1997042138A1 (en) * | 1996-05-03 | 1997-11-13 | Eastman Chemical Company | Explosive formulations |
WO1997042140A1 (en) * | 1996-05-03 | 1997-11-13 | Eastman Chemical Company | Explosive formulations |
US5936196A (en) * | 1996-05-03 | 1999-08-10 | Eastman Chemical Co. | Explosive formulations |
WO1997042137A1 (en) * | 1996-05-06 | 1997-11-13 | Eastman Chemical Company | Explosive formulations |
US5808234A (en) * | 1996-05-06 | 1998-09-15 | Eastman Chemical Company | Explosive formulations |
WO1998016485A1 (en) * | 1996-10-15 | 1998-04-23 | Eastman Chemical Company | Explosive formulations |
US5801326A (en) * | 1997-04-18 | 1998-09-01 | Eastman Chemical Company | Explosive formulations |
RU2451650C1 (en) * | 2010-12-20 | 2012-05-27 | Федеральное государственное унитарное предприятие "Научно-исследовательский институт полимерных материалов" | Method of octogene modification |
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