GB601101A - Improvements in or relating to synthetic resins - Google Patents

Improvements in or relating to synthetic resins

Info

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
Application number
GB768142A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Filing date
Publication date
Application filed by Individual filed Critical Individual
Publication of GB601101A publication Critical patent/GB601101A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G16/00Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00
    • C08G16/02Condensation polymers of aldehydes or ketones with monomers not provided for in the groups C08G4/00 - C08G14/00 of aldehydes
    • C08G16/0212Condensation 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
    • C08G16/0218Condensation 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
    • C08G16/0231Condensation 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
    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B45/00Compositions or products which are defined by structure or arrangement of component of product
    • C06B45/04Compositions 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
    • C06B45/06Compositions 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
    • C06B45/10Compositions 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
    • C06B45/105The 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.
GB768142A 1942-06-05 Improvements in or relating to synthetic resins Expired GB601101A (en)

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)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3071617A (en) * 1948-06-01 1963-01-01 Purdue Research Foundation Nitro plastic propellants

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3071617A (en) * 1948-06-01 1963-01-01 Purdue Research Foundation Nitro plastic propellants

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