GB601101A - Improvements in or relating to synthetic resins - Google Patents
Improvements in or relating to synthetic resinsInfo
- Publication number
- GB601101A GB601101A GB768142A GB768142A GB601101A GB 601101 A GB601101 A GB 601101A GB 768142 A GB768142 A GB 768142A GB 768142 A GB768142 A GB 768142A GB 601101 A GB601101 A GB 601101A
- Authority
- GB
- United Kingdom
- Prior art keywords
- nitro
- nitropropane
- alkaline
- reaction
- dimethylol
- 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
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G16/00—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00
- C08G16/02—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes
- C08G16/0212—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes with acyclic or carbocyclic organic compounds
- C08G16/0218—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes with acyclic or carbocyclic organic compounds containing atoms other than carbon and hydrogen
- C08G16/0231—Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes with acyclic or carbocyclic organic compounds containing atoms other than carbon and hydrogen containing nitrogen
-
- 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
- C06B45/04—Compositions or products which are defined by structure or arrangement of component of product comprising solid particles dispersed in solid solution or matrix not used for explosives where the matrix consists essentially of nitrated carbohydrates or a low molecular organic explosive
- C06B45/06—Compositions or products which are defined by structure or arrangement of component of product comprising solid particles dispersed in solid solution or matrix not used for explosives where the matrix consists essentially of nitrated carbohydrates or a low molecular organic explosive the solid solution or matrix containing an organic component
- C06B45/10—Compositions or products which are defined by structure or arrangement of component of product comprising solid particles dispersed in solid solution or matrix not used for explosives where the matrix consists essentially of nitrated carbohydrates or a low molecular organic explosive the solid solution or matrix containing an organic component the organic component containing a resin
- C06B45/105—The resin being a polymer bearing energetic groups or containing a soluble organic explosive
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dispersion Chemistry (AREA)
- Molecular Biology (AREA)
- Crystallography & Structural Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Combustible synthetic resins are produced by condensation of a compound of formula RCX2NO2 (where R is H, alkyl, alkylol or aryl, and X is H or CH2OH with an aliphatic aldehyde in neutral, acid or alkaline medium at a temperature between room temperature and 150 DEG C. Suitable compounds are nitro-paraffins, e.g. nitromethane, nitroethane or 1-nitropropane; phenylnitromethane, or nitro alcohols containing secondary or tertiary nitro groups such as b -nitro-ethanol; b -nitro-propanol; di-methylol nitro-ethane; di-methylol nitro-propane. Mixtures of compounds may be used. Formaldehyde is the preferred aldehyde. Strong or weak alkalies, basic salts and/or nitrogen bases or salts of nitrogen bases may be used to adjust the reaction medium to the desired pH. Nitrogenous bases are said to take part in the formation of the resin. The reaction may be performed in aqueous or non-aqueous solvents or the reactants may be emulsified. In example I a resin is prepared from formaldehyde, ammonia and 1-nitropropane, the reaction medium becoming neutral or even slightly acidic as the ammonia is taken up by the resin. Example II is similar but has an alkaline reaction medium due to a greater proportion of ammonia. Example III is similar, oily products formed as a result of the initial stages of the reaction being removed before completion of resinification. In example IV hexamethylenetetramine is present to produce an alkaline medium. In example V an ammonium salt and some free acid is present to yield an acid reaction medium. In example VI sodium bicarbonate is used to make the medium alkaline. Example VII is similar to example I but performs the reaction in water-xylene emulsion. In example VIII the reaction medium is alkaline and alcoholic. In example IX, dimethylol nitropropane, formaldehyde and ammonia are condensed together. Example X uses dimethylol nitroethane, example XI b -nitrobutanol and example XII a mixture of b -nitrobutanol and dimethylolpropane. In example XIII dimethylol nitropropane is employed and in example XIV a mixture of dimethylol nitropropane and monomethylol nitropropane. The resins are soluble in liquid aromatic nitrocompounds, e.g. nitrobenzenes, nitrotoluenes, nitroxylenes and nitrophenols and in liquid nitric acid esters, e.g. nitroglycol nitroglycerine and molten pentaerythritol tetranitrate. They may be used as ingredients of high explosives, propellants or pyrotechnic mixtures.
Publications (1)
Publication Number | Publication Date |
---|---|
GB601101A true GB601101A (en) | 1948-04-28 |
Family
ID=1629065
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB768142A Expired GB601101A (en) | 1942-06-05 | Improvements in or relating to synthetic resins |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB601101A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3071617A (en) * | 1948-06-01 | 1963-01-01 | Purdue Research Foundation | Nitro plastic propellants |
-
1942
- 1942-06-05 GB GB768142A patent/GB601101A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3071617A (en) * | 1948-06-01 | 1963-01-01 | Purdue Research Foundation | Nitro plastic propellants |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3873579A (en) | Organic azides and method of preparation thereof | |
US2485855A (en) | Nitramines | |
GB601101A (en) | Improvements in or relating to synthetic resins | |
US2381408A (en) | Nitro amines and process for preparing same | |
US2419043A (en) | Combustible synthetic resins | |
US3526667A (en) | Process for acetal preparation | |
GB2355714A (en) | Ammonium 3,5-diaminopicrate | |
US2330112A (en) | Nitroethyl nitrate derivative | |
US1936020A (en) | Method of nitrating organic substances | |
GB743446A (en) | Improvements in or relating to aromatic 2-aminoalkanediols-(1.3) | |
US2261788A (en) | Process for the preparation of a composition of trimethylolnitromethane | |
GB616337A (en) | Improvements in or relating to synthetic resins | |
Ungnade et al. | β, β-Dinitroalkylamines and-nitramines, and Related Compounds1 | |
US1691955A (en) | Explosive | |
McKay et al. | The Nitration Products of 2-Nitramino-Δ2-1, 3-diazacycloalkenes | |
US3714260A (en) | 4,4-bis (difluoramino)-1,7-difluoro-1,1,7,7-tetranitroheptane | |
US1560427A (en) | Explosive and process of making same | |
Hass | Recent developments in nitroparaffins | |
US3316311A (en) | Process for preparing polynitrohydro-carbons from nitrohydrocarbons and tetranitromethane in alkaline solution | |
US3049570A (en) | Explosive composition | |
GB491648A (en) | Improvements relating to diesel fuels | |
AU5825901A (en) | Method for producing dinitro-diaza-alkanes and intermediate products hereto | |
US2152372A (en) | Nitrated pentaerythritol motherliquor | |
US4513148A (en) | Method for the preparation of methylnitramine | |
US3390181A (en) | Process for preparing nu-nitro-nu-fluoro-amines |