GB616337A - Improvements in or relating to synthetic resins - Google Patents
Improvements in or relating to synthetic resinsInfo
- Publication number
- GB616337A GB616337A GB360643A GB360643A GB616337A GB 616337 A GB616337 A GB 616337A GB 360643 A GB360643 A GB 360643A GB 360643 A GB360643 A GB 360643A GB 616337 A GB616337 A GB 616337A
- Authority
- GB
- United Kingdom
- Prior art keywords
- nitro
- diamine
- nitropropane
- formaldehyde
- ethylene diamine
- 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
-
- 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
- C08G12/00—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
- C08G12/02—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
- C08G12/04—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds
- C08G12/22—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with acyclic or carbocyclic compounds with carboxylic acid amides
-
- 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
- C08G12/00—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
- C08G12/02—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
- C08G12/40—Chemically modified polycondensates
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dispersion Chemistry (AREA)
- Molecular Biology (AREA)
- Crystallography & Structural Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Thermoplastic self - combustible synthetic resins are prepared by condensing a compound of the general formula RCX2NO2 (where R denotes H, alkyl or aryl and X denotes H or CH2OH) with an aliphatic aldehyde in the presence of diamines or diamides containing primary or secondary amino groups at temperatures between room temperature and 150 DEG C. Suitable diamines or diamides are ethylene diamine, trimethylene diamine, hexa-methylene diamine, phenylene diamine, tolylene diamine, piperazine, urea, methyl oxamide. They may be used individually or as mixtures if desired with ammonia and/or monoamines. Suitable nitro compounds are nitromethane, nitro-ethane, 1-nitro-propane, phenyl nitro-methane, or nitro-alcohols with secondary or tertiary nitro groups. The reaction may be carried out in alkaline medium or in slightly alkaline medium becoming acid during the course of the reaction, or the medium may be acid if a salt of a diamine is employed. The reactants may be dissolved in aqueous or non-aqueous media or emulsified. In the examples: (1) 1-nitropropane is reacted with formaldehyde and ethylene diamine at 30 DEG C., and the resin separated, washed and dried. Impurities may be removed by steam distillation. (2) Ammonia is added to the reaction mixture of example (1). (3) Dimethylol nitropropane, ethylene diamine and formaldehyde are reacted together. (4) Dimethylol nitrobutane and ethylene diamine are reacted together. (5) b -Nitrobutanol, dimethylol nitropropane, formaldehyde and ethylene diamine are reacted together. (6) Nitropropane, hexamethylene diamine and formaldehyde are reacted together. The products are soluble in nitro aromatic compounds, or nitrates such as nitro-glycerine or pentaerythritol tetranitrate. They will gelatinise nitro-cellulose and cellulose acetate. Specification 601,101 is referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB360643A GB616337A (en) | 1943-03-04 | 1943-03-04 | Improvements in or relating to synthetic resins |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB360643A GB616337A (en) | 1943-03-04 | 1943-03-04 | Improvements in or relating to synthetic resins |
Publications (1)
Publication Number | Publication Date |
---|---|
GB616337A true GB616337A (en) | 1949-01-20 |
Family
ID=9761499
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB360643A Expired GB616337A (en) | 1943-03-04 | 1943-03-04 | Improvements in or relating to synthetic resins |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB616337A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2452501A1 (en) * | 1979-03-30 | 1980-10-24 | Int Minerals & Chem Corp | |
FR2463225A1 (en) * | 1979-08-03 | 1981-02-20 | Int Minerals & Chem Corp | CROSSLINKING AGENT COMPOSITION, ESPECIALLY UREA-ALDEHYDE RESIN, MODIFIED BY NITROALCANOL AND / OR NITROALCANE AND ITS USE FOR REDUCING THE RESIDUAL CONTENT OF FREE ALDEHYDE AND FOR TREATING WOVEN OR NONWOVEN TEXTILES |
-
1943
- 1943-03-04 GB GB360643A patent/GB616337A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2452501A1 (en) * | 1979-03-30 | 1980-10-24 | Int Minerals & Chem Corp | |
FR2463225A1 (en) * | 1979-08-03 | 1981-02-20 | Int Minerals & Chem Corp | CROSSLINKING AGENT COMPOSITION, ESPECIALLY UREA-ALDEHYDE RESIN, MODIFIED BY NITROALCANOL AND / OR NITROALCANE AND ITS USE FOR REDUCING THE RESIDUAL CONTENT OF FREE ALDEHYDE AND FOR TREATING WOVEN OR NONWOVEN TEXTILES |
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