GB763438A - Improvements in or relating to explosives - Google Patents
Improvements in or relating to explosivesInfo
- Publication number
- GB763438A GB763438A GB30856/52A GB3085652A GB763438A GB 763438 A GB763438 A GB 763438A GB 30856/52 A GB30856/52 A GB 30856/52A GB 3085652 A GB3085652 A GB 3085652A GB 763438 A GB763438 A GB 763438A
- Authority
- GB
- United Kingdom
- Prior art keywords
- trinitroethanol
- ester
- acid
- reacted
- trinitroethyl
- 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
Links
Classifications
-
- 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
- C06B25/36—Compositions containing a nitrated organic compound the compound being a nitroparaffin
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention comprises an explosive consisting of or comprising a trinitroethanol derivative having the grouping C(NO2)3, said derivative being an ester of trinitroethanol with an organic or inorganic acid or a nitrated trinitroethanol ester of said organic acid, or a trinitroethanol derivative of urea or melamine or an ammonia derivative of trinitroethanol, said ester, nitrated ester, or urea, melamine, or ammonia derivative being one which is capable of predetermined detonation and having a ratio of carbon atoms to oxygen atoms of less than 2 : 1. The explosives may be used either alone or mixed with one or more other explosives and other balance substances (see Group XXI). In examples: (1) crotonic acid is reacted under reflux with phosphorus pentachloride and when the mixture has cooled trinitroethanol is added and the mixture heated to 50 DEG C. and after cooling poured into water when the ester [(NO2)3C. C5H7O2] separates as an oil; (2) the chloride or the amide of benzoic acid is reacted with trinitroethanol to yield the trinitroethyl ester of benzoic acid; (3) the product of (2) is nitrated with a mixture of nitric and sulphuric acid at below 40 DEG C. to yield the trinitroethyl ester of mononitro benzoic acid; (4) adipic acid chloride is reacted with trinitroethanol to yield the dinitroethyl ester of adipic acid; (5) the ditrinitroethyl ester of phthalic acid is obtained from the alcohol and phthalic acid chloride and the ester may be nitrated; (6) nitroform, formaldehyde and ammonia are reacted to form ditrinitroethylamine which is then nitrated to form ditrinitroethyl nitramine; (7) nitroform, formaldehyde and urea are reacted in aqueous solution to form ditrinitroethyl urea; (8) melamine and trinitroethanol are reacted in aqueous solution to form tris (trinitroethyl) melamine; (9) trinitroethanol dissolved in carbon tetrachloride is reacted with phosphorus pentachloride to form trinitroethyl phosphate together with some trinitroethyl chloride; (10) trinitroethyldinitroacetate is obtained by adding trinitroethyl acetate to nitrating acid and then pouring the mixture into ice water. The stability and explosive characteristics of the various products are described and examples are also given of various mixtures of the products with known explosives (see Group XXI). Other organic acids mentioned are unsaturated dibasic and polybasic acids. Reference has been directed by the Comptroller to Specifications 698,138 and 729,469.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE763438X | 1951-12-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB763438A true GB763438A (en) | 1956-12-12 |
Family
ID=20329930
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB30856/52A Expired GB763438A (en) | 1951-12-06 | 1952-12-05 | Improvements in or relating to explosives |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB763438A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2511370C2 (en) * | 2012-07-04 | 2014-04-10 | Николай Евгеньевич Староверов | Rocket propellant or explosive substance and method of its preparation (versions) |
RU2552745C1 (en) * | 2013-11-19 | 2015-06-10 | Николай Евгеньвич Староверов | Explosive substance (versions) |
-
1952
- 1952-12-05 GB GB30856/52A patent/GB763438A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2511370C2 (en) * | 2012-07-04 | 2014-04-10 | Николай Евгеньевич Староверов | Rocket propellant or explosive substance and method of its preparation (versions) |
RU2552745C1 (en) * | 2013-11-19 | 2015-06-10 | Николай Евгеньвич Староверов | Explosive substance (versions) |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB763438A (en) | Improvements in or relating to explosives | |
US2139364A (en) | Alpha-substituted glycerol nitrates | |
US3071617A (en) | Nitro plastic propellants | |
US3310444A (en) | Monopropellant comprising a difluoraminoalkane and fuming nitric acid | |
US2355770A (en) | Preparation of cyclo-trimethylenetrinitramine | |
US2997501A (en) | 1, 3-dinitro-1, 3-dimethyl urea | |
US2736742A (en) | Method of processing acid nitrated organic products | |
GB616453A (en) | Improvements in or relating to the production of nitropolystyrene | |
US2330112A (en) | Nitroethyl nitrate derivative | |
US3369020A (en) | 1, 4-diformyl-2, 3, 5, 6-tetrakis(difluoramino)piperazines | |
US1686344A (en) | Diethylene glycol dinitrate and process of preparing same | |
US3070473A (en) | Liquid propellants | |
US2443903A (en) | Nitratoalkyl amides | |
US2978483A (en) | Nitraza dinitrile compositions of matter | |
GB1317498A (en) | Process for the manufacture of n,n-di-haloalkyl-2-nitro-4- substitutet tertiary anomatic amines | |
GB968848A (en) | Plasticizers and plasticized resinous compositions | |
RU2464254C1 (en) | Liquid explosive formation method | |
US1166546A (en) | Process of producing a liquid explosive. | |
GB601101A (en) | Improvements in or relating to synthetic resins | |
JAIN et al. | Some mechanistic aspects of hypergolic ignition- Reaction of dinitrogen tetroxide with solid amines and their mixtures with magnesium | |
GB586012A (en) | Improvements in or relating to plastic detonating explosive compositions | |
US674292A (en) | Method of making explosives. | |
HUP0000354A1 (en) | Nitration process | |
GB616337A (en) | Improvements in or relating to synthetic resins | |
US3575973A (en) | Compounds containing a dinitrofluoromethyl group |