GB1156703A - Gelling of Nitric Acid - Google Patents

Gelling of Nitric Acid

Info

Publication number
GB1156703A
GB1156703A GB40185/66A GB4018566A GB1156703A GB 1156703 A GB1156703 A GB 1156703A GB 40185/66 A GB40185/66 A GB 40185/66A GB 4018566 A GB4018566 A GB 4018566A GB 1156703 A GB1156703 A GB 1156703A
Authority
GB
United Kingdom
Prior art keywords
nitric acid
ammonium
diallyl
ions
gelled
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
GB40185/66A
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority claimed from US575986A external-priority patent/US3361601A/en
Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of GB1156703A publication Critical patent/GB1156703A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B47/00Compositions in which the components are separately stored until the moment of burning or explosion, e.g. "Sprengel"-type explosives; Suspensions of solid component in a normally non-explosive liquid phase, including a thickened aqueous phase
    • C06B47/14Compositions in which the components are separately stored until the moment of burning or explosion, e.g. "Sprengel"-type explosives; Suspensions of solid component in a normally non-explosive liquid phase, including a thickened aqueous phase comprising a solid component and an aqueous phase
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B21/00Nitrogen; Compounds thereof
    • C01B21/20Nitrogen oxides; Oxyacids of nitrogen; Salts thereof
    • C01B21/38Nitric acid
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B21/00Nitrogen; Compounds thereof
    • C01B21/20Nitrogen oxides; Oxyacids of nitrogen; Salts thereof
    • C01B21/38Nitric acid
    • C01B21/46Purification; Separation ; Stabilisation
    • CCHEMISTRY; METALLURGY
    • C06EXPLOSIVES; MATCHES
    • C06BEXPLOSIVES OR THERMIC COMPOSITIONS; MANUFACTURE THEREOF; USE OF SINGLE SUBSTANCES AS EXPLOSIVES
    • C06B47/00Compositions in which the components are separately stored until the moment of burning or explosion, e.g. "Sprengel"-type explosives; Suspensions of solid component in a normally non-explosive liquid phase, including a thickened aqueous phase

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Catalysts (AREA)

Abstract

1,156,703. Gelled nitric acid; explosive compositions. E. I. DU PONT DE NEMOURS & CO. 8 Sept., 1966 [9 Sept., 1965; 23 Oct., 1965; 30 Aug., 1966], No. 40185/66. Headings C1A and ClD. [Also in Division C3] Aqueous nitric acid is gelled by copolymerizing in situ in the nitric acid a mixture of unsaturated monomers comprising (a) up to 20%, based on the weight of the nitric acid, of a monomer of the formula CH 2 = CRX and/or a monovinyl pyridine, and (b) up to 30%, based on the weight of (a), of a monomer having at least two terminal unsaturated methylene groups. In monomer (a) X is -CN, -COOR, -CONR 2 , or COOM, M is ammonium, alkali metal, or alkaline earth metal, and R is hydrogen or lower alkyl which may be hydroxy- or cyano-substituted. Many suitable monomers are listed, examples of (a) being acrylonitrile, acrylamide, acrylic acid, methacrylic acid, 4- vinyl pyridine, and 2-methyl-o-vinyl pyridine; and of (b) N,N<SP>1</SP> - methylene - bis - acrylamide, N,N<SP>1</SP>,N<SP>11</SP> - triacrylyl - hexahydro - s - triazine, tetramethylene glycol dimethacrylate, trimethylene propane trimethacrylate, ethylene glycol dimethacrylate, divinyl benzene, allyl acrylate, N-allyl methacrylamide, diallyl ether, diallyl adipate, diallyl maleate, diallyl ether of pentaerythritol, diallylamine, N,N<SP>1</SP>-diallyl adipamide, N-allyl acrylamide, and vinyl methacrylate. The copolymer, may be formed by free radical catalysis, using as promoters ammonium or alkali metal persulphates, perborates, or pervanadates, to which may be added hydrogen peroxide, hydrazine, hydroxylamine, or carbohydrazide, and also copper, silver, ferrous, or cobaltous ions; other catalysts referred to are hydrogen peroxide with ferrous ions, cobaltic ions with or without hydrazine and persulphate ions, and organic azo compounds and peroxides, several of which are specified. Detonating explosive compositions containing the gelled nitric acid may also include the following ingredients:-nitrobenzene, nitrotoluenes, liquid and solid hydrocarbons, cellulose and starch products, sugar, silicon, ferrosilicon, sulphur, and aluminium as non-explosive fuels; RDX, nitrocellulose, smokeless powder, and TNT as explosive sensitizers; and ammonium, sodium, and potassium nitrates, ammonium and potassium sulphates and acetates, and potassium mono-hydrogen phosphate as oxidizing salts. In making the gel, nitric acid of strength 5- 99% by weight may be sparged with nitrogen to remove oxygen and oxides of nitrogen, and then mixed with the other components, the mixture being cooled if necessary; gels of varying viscosity may be produced, ranging from flowing pourable masses to rigid bodies. Apart from its use in explosives, the gel may be used for etching and other metallurgical uses, in chemical synthesis, including the manufacture of fertilizers, and for acidifying in mineralogical processes.
GB40185/66A 1965-09-09 1966-09-08 Gelling of Nitric Acid Expired GB1156703A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US48622365A 1965-09-09 1965-09-09
US50416965A 1965-10-23 1965-10-23
US575986A US3361601A (en) 1966-08-30 1966-08-30 Gelled aqueous nitric acid compositions

Publications (1)

Publication Number Publication Date
GB1156703A true GB1156703A (en) 1969-07-02

Family

ID=27413731

Family Applications (1)

Application Number Title Priority Date Filing Date
GB40185/66A Expired GB1156703A (en) 1965-09-09 1966-09-08 Gelling of Nitric Acid

Country Status (8)

Country Link
AT (1) AT289621B (en)
BE (1) BE686613A (en)
CH (1) CH497340A (en)
DE (1) DE1567775A1 (en)
FR (2) FR1497679A (en)
GB (1) GB1156703A (en)
IL (1) IL26485A (en)
OA (1) OA02133A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2654971C1 (en) * 2017-03-23 2018-05-23 Акционерное общество "Объединенная химическая компания "УРАЛХИМ" (АО "ОХК "УРАЛХИМ") Mixed liquid explosive substance

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2654971C1 (en) * 2017-03-23 2018-05-23 Акционерное общество "Объединенная химическая компания "УРАЛХИМ" (АО "ОХК "УРАЛХИМ") Mixed liquid explosive substance

Also Published As

Publication number Publication date
AT289621B (en) 1971-04-26
BE686613A (en) 1967-02-15
FR93846E (en) 1969-05-23
FR1497679A (en) 1967-10-13
CH497340A (en) 1970-10-15
IL26485A (en) 1970-05-21
DE1567775A1 (en) 1970-08-20
OA02133A (en) 1970-05-05

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