US2997501A - 1, 3-dinitro-1, 3-dimethyl urea - Google Patents
1, 3-dinitro-1, 3-dimethyl urea Download PDFInfo
- Publication number
- US2997501A US2997501A US811000A US81100059A US2997501A US 2997501 A US2997501 A US 2997501A US 811000 A US811000 A US 811000A US 81100059 A US81100059 A US 81100059A US 2997501 A US2997501 A US 2997501A
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- Prior art keywords
- dinitro
- dimethyl urea
- colloidal
- urea
- nitrocellulose
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- 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.)
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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
-
- 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
- C06B25/18—Compositions containing a nitrated organic compound the compound being nitrocellulose present as 10% or more by weight of the total composition
Definitions
- the present invention relates to 1.3-dinitro-L3-dimethyl urea and the production method thereof, and further explosive compositions characterized by containing same.
- 1.3-dinitro-L3-dimethyl urea is a compound in the state of a liquid nonvolatile at normal temperature, which is obtainable by nitrifying 1.3-dimethyl urea by the medium of concentrated nitric acid or concentrated nitric acid and acetic anhydride, having a structural formula as follows:
- the present invention is characterized by the fact that l.3-d.initro-1.3-dimethyl urea has such an excellent feature as material for gunpowder and powder compositions, obtained by adding a small amount thereof to powder matter such as ammonium nitrate or ammonium perchlorate to be efiective as explosives, and also a colloidal matter obtained by admixing 1.3-dinitro-1.3-dimethyl urea with nitrocellulose, or powder or colloidal compositions obtained by compounding a liquid or powder matter to such colloidal matter to be effective as explosives, shooting agent for guns and rocket propelling agent, thus not only providing an excellent feature, but rendering its production extremely safe and easy.
- nitroglycerin or nitroglycol is an extremely unsteady compound liable to blast by a slight shock or friction, accompanying a considerable danger in its production and handling.
- many attempts have been made to produce colloidal gunpowders by employing matters of better stability as materials, however, in most examples resins of bad oxygen balance have been adopted as gelatinizer or plasticizer and those gunpowders have generalally been found considerably inferior at the point of capacity.
- the subject 1.3-dinitro-1.3-dimethyl urea has a fine property as materials of gunpowder, especially a colloidal one, as described above, and the various explosive compositions comprising same are safe and easy in the production thereof with capacity superior to others when compared with heretofore known gunpowders employing nitroglycerin, therefore the great value of the present invention is readily apparent.
- Example 1 This example relates to the production method of 1.3- dinitro-l.3-dimethyl urea.
- Example 2 The following examples are respectively relating to explosive compounds comprising 1.3-dinitro-L3-dimethyl urea.
- Powder compositions consist of ammonium nitrate 60 g., ammonium perchlorate 30 g. and 1.3-diuitro-L3-dimethyl urea 10 g. Being adequate as explosives, the angle of deviation of mortar according to the ballistic mortar test is 1920.
- Example 3 A colloidal composition is composed of 1.3'dinitro- 1.3-dimetl1yl urea g. and nitrocellulose 10 g. Being adequate as explosives, the angle of deviation of mortar according to the ballistic mortar test is 1820".
- Example 4 A colloidal composition of plasticizing property is obtained by admixing ammonium nitrate 50 g. with colloidal matter consisting of 1.3-dinitro-1.3-dimethyl urea 31 g., nitroglycerin 15' g. and nitrocellulose 4 g. Being adequate as explosives, the angle of deviation of mortar according to the ballistic mortar test is 1904.
- Example 5 A solid colloidal composition is composed of 1.3-dini tro-1.3-dimethyl urea 43 g., nitrocellulose 50 g. and ethylcentralite 7 g. Being adequate as shooting agent for guns and rocket propelling agent, even under high pressure in the combustion chamber of rocket combustion quality the composition is stabilized without fear of explosion.
- Example 6 A colloidal composition with plasticizing property consists of 1.3-dinitro-L3-dimethyl urea 31 g., nitrocellulose 4 g. and ammonium nitrate 65 g. Being adequate as explosives, the angle of deviation of mortar according to the ballistic mortar test is 1816.
- Example 7 A colloidal composition with plasticizing property is composed of 1.3-dinitro-l.3-dimethyl urea 33 g.,, nitrocellulose 5 g., ammonium nitrate 45 g. and ammonium perchlorate l7 g. Being adequate as explosives, the angle of deviation of mortar according to the ballistic mortar test is 1850.
- Example 8 A powder composition consists of 1.3-dinitro-1.3-dimethyl urea 16 g., nitrocellulose 2 g. and ammonium nitrate 82 g. Being adequate as explosives, the angle of deviation of mortar according to the ballistic mortar test is 1812. 1 Further, the ballistic mortar test was conducted by using a sample of 10 g., and the angle of deviation of mortar for trinitro toluene is 1524 under the same conditions.
- a method of producing 1.3-dinitro-L3-dimethyl urea comprising the step of nitrifying 1.3-dimethyl urea with concentrated nitric acid at a temperature of below 30 C.
- a method of producing 1.3-dinitro-L3-dim'ethyl urea comprising the step of nitrifying 1.3-dimethyl'urea with concentrated nitric acid and acetic anhydride at a temperature of below 30 C.
Description
United States atent 2,997,50l Patented Aug. 22, 1961 ice 2,997,501 LB-DINITRO-LS-DIMEI'HYL UREA Kazuo Shiino, 366 Yazu, Odawara-city, Kanagawa-lren, Japan, and Senzo Ikinuma, 524 Sumiyajijo, Minami Ashigara-cho, Ashigarakami-gun, Kanagawa-ken, Japan No Drawing. Filed May 5, 1959, Ser. No. 811,000
Claims priority, application Japan Aug. 4, 1958 3"Claims. (Cl. 260-553) The present invention relates to 1.3-dinitro-L3-dimethyl urea and the production method thereof, and further explosive compositions characterized by containing same.
1.3-dinitro-L3-dimethyl urea is a compound in the state of a liquid nonvolatile at normal temperature, which is obtainable by nitrifying 1.3-dimethyl urea by the medium of concentrated nitric acid or concentrated nitric acid and acetic anhydride, having a structural formula as follows:
NO: I l-CH NCHa This is a compound unknown in the heretofore published literature, containing a great amount of oxygen efiective as a gunpowder and it can be easily exploded in itself by regular industrial detonation cap, producing an explosive power bigger than that of tetryl. Further, it is extremely insensitive to shock and friction and according to the sensitivity test, conducted by a falling hammer, it is shown that its inexplosive point is ten times higher than nitroglycerin. Still further, it has a nature of dissolving numerous organic compounds, especially, when admixed with nitrocellulose, it yields a colloidal matter; this colloidal matter can be brought to any solidity, by varying the ratio of admixture with nitrocellulose.
The present invention is characterized by the fact that l.3-d.initro-1.3-dimethyl urea has such an excellent feature as material for gunpowder and powder compositions, obtained by adding a small amount thereof to powder matter such as ammonium nitrate or ammonium perchlorate to be efiective as explosives, and also a colloidal matter obtained by admixing 1.3-dinitro-1.3-dimethyl urea with nitrocellulose, or powder or colloidal compositions obtained by compounding a liquid or powder matter to such colloidal matter to be effective as explosives, shooting agent for guns and rocket propelling agent, thus not only providing an excellent feature, but rendering its production extremely safe and easy.
Heretofore, a colloidal matter obtained from organic nitric acid ester and nitrocellulose or one with addition thereto of various compounding agents has widely been used as gunpowder, however, it is commonly known that nitroglycerin or nitroglycol is an extremely unsteady compound liable to blast by a slight shock or friction, accompanying a considerable danger in its production and handling. And therefore, many attempts have been made to produce colloidal gunpowders by employing matters of better stability as materials, however, in most examples resins of bad oxygen balance have been adopted as gelatinizer or plasticizer and those gunpowders have generalally been found considerably inferior at the point of capacity.
Whereas, in the present invention the subject 1.3-dinitro-1.3-dimethyl urea has a fine property as materials of gunpowder, especially a colloidal one, as described above, and the various explosive compositions comprising same are safe and easy in the production thereof with capacity superior to others when compared with heretofore known gunpowders employing nitroglycerin, therefore the great value of the present invention is readily apparent.
Example 1 This example relates to the production method of 1.3- dinitro-l.3-dimethyl urea.
15 g. of 1.3-dimethyl urea is added bit by bit to the admixture of concentrated nitric acid of 45 u. and acetic anhydride of 60 u., while agitating it, keeping the temperature at about 5 C., and after said addition agitation is still continued for 30 minutes, and thereafter ether is extracted by pouring it in ice water. After washing the ether solution in the order or water, dilution of the solution of sodium carbonate and water, ether is distilled out at normal temperature, and when the residue of oil mat ter is dried by anhydrous sodium sulfate a liquid almost uncolored can be obtained having a weight of 26 g. In case of using concentrated nitric acid only in the nitrification, the yield is about 18 g. under the same conditions.
Elementary analysis values of the product are: C =20.58%, H=3.16%, N=31.52%, and the value of molecular weight measured by means of an antifreezing method employing benzene is 172.3, thus well corresponding, respectively, with a theoretical value as of CO(N.NO .CH
Example 2 The following examples are respectively relating to explosive compounds comprising 1.3-dinitro-L3-dimethyl urea.
Powder compositions consist of ammonium nitrate 60 g., ammonium perchlorate 30 g. and 1.3-diuitro-L3-dimethyl urea 10 g. Being adequate as explosives, the angle of deviation of mortar according to the ballistic mortar test is 1920.
Example 3 A colloidal composition is composed of 1.3'dinitro- 1.3-dimetl1yl urea g. and nitrocellulose 10 g. Being adequate as explosives, the angle of deviation of mortar according to the ballistic mortar test is 1820".
Example 4 A colloidal composition of plasticizing property is obtained by admixing ammonium nitrate 50 g. with colloidal matter consisting of 1.3-dinitro-1.3-dimethyl urea 31 g., nitroglycerin 15' g. and nitrocellulose 4 g. Being adequate as explosives, the angle of deviation of mortar according to the ballistic mortar test is 1904.
Example 5 A solid colloidal composition is composed of 1.3-dini tro-1.3-dimethyl urea 43 g., nitrocellulose 50 g. and ethylcentralite 7 g. Being adequate as shooting agent for guns and rocket propelling agent, even under high pressure in the combustion chamber of rocket combustion quality the composition is stabilized without fear of explosion.
Example 6 A colloidal composition with plasticizing property consists of 1.3-dinitro-L3-dimethyl urea 31 g., nitrocellulose 4 g. and ammonium nitrate 65 g. Being adequate as explosives, the angle of deviation of mortar according to the ballistic mortar test is 1816.
Example 7 A colloidal composition with plasticizing property is composed of 1.3-dinitro-l.3-dimethyl urea 33 g.,, nitrocellulose 5 g., ammonium nitrate 45 g. and ammonium perchlorate l7 g. Being adequate as explosives, the angle of deviation of mortar according to the ballistic mortar test is 1850.
3 Example 8 A powder composition consists of 1.3-dinitro-1.3-dimethyl urea 16 g., nitrocellulose 2 g. and ammonium nitrate 82 g. Being adequate as explosives, the angle of deviation of mortar according to the ballistic mortar test is 1812. 1 Further, the ballistic mortar test was conducted by using a sample of 10 g., and the angle of deviation of mortar for trinitro toluene is 1524 under the same conditions.
While we have discovered several embodiments of the present invention, it is to be understood that these embodiments are given by example only and not in a limit- What we claim is:
1. 1.3-dinitro-l.3-dimethyl urea.
2. A method of producing 1.3-dinitro-L3-dimethyl urea comprising the step of nitrifying 1.3-dimethyl urea with concentrated nitric acid at a temperature of below 30 C.
3. A method of producing 1.3-dinitro-L3-dim'ethyl urea comprising the step of nitrifying 1.3-dimethyl'urea with concentrated nitric acid and acetic anhydride at a temperature of below 30 C.
ing sense, the scope of the present invention being de- 15 termined by the objects and tthe claims.
References Cited in the file of this patent 7 Davis et al.: J. Am. Chem. Soc., vol. 58, vp. 1800-3 (1936). Singh: J. Indian Chem. Soc., vol. 31, pp; 355-8 (1954).
Claims (1)
1. 1.3-DINITRO-1.3-DIMETHYL UREA.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2997501X | 1958-08-04 |
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US2997501A true US2997501A (en) | 1961-08-22 |
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US811000A Expired - Lifetime US2997501A (en) | 1958-08-04 | 1959-05-05 | 1, 3-dinitro-1, 3-dimethyl urea |
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3166451A (en) * | 1963-03-22 | 1965-01-19 | Grace W R & Co | Sensitizing agents comprising the reaction product of urea-formaldehyde-hydrogen peroxide |
US3172793A (en) * | 1965-03-09 | Temperature xc | ||
US3326976A (en) * | 1963-12-11 | 1967-06-20 | Du Pont | Fluorinated gem-diamines and fluorinated gem-alkyldiamines and the process for theirpreparation |
US4513148A (en) * | 1982-07-01 | 1985-04-23 | The United States Of America As Represented By The Secretary Of The Navy | Method for the preparation of methylnitramine |
CN108440335A (en) * | 2018-03-22 | 2018-08-24 | 西安近代化学研究所 | A kind of synthetic method of methyl-nitramine |
-
1959
- 1959-05-05 US US811000A patent/US2997501A/en not_active Expired - Lifetime
Non-Patent Citations (1)
Title |
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None * |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3172793A (en) * | 1965-03-09 | Temperature xc | ||
US3166451A (en) * | 1963-03-22 | 1965-01-19 | Grace W R & Co | Sensitizing agents comprising the reaction product of urea-formaldehyde-hydrogen peroxide |
US3326976A (en) * | 1963-12-11 | 1967-06-20 | Du Pont | Fluorinated gem-diamines and fluorinated gem-alkyldiamines and the process for theirpreparation |
US4513148A (en) * | 1982-07-01 | 1985-04-23 | The United States Of America As Represented By The Secretary Of The Navy | Method for the preparation of methylnitramine |
CN108440335A (en) * | 2018-03-22 | 2018-08-24 | 西安近代化学研究所 | A kind of synthetic method of methyl-nitramine |
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