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USH990H - Recrystallization of 3-nitro-1,2,4-triazol-5-one from dimethylsulfoxide and methylene chloride - Google Patents

Recrystallization of 3-nitro-1,2,4-triazol-5-one from dimethylsulfoxide and methylene chloride Download PDF

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Publication number
USH990H
USH990H US07/386,378 US38637889A USH990H US H990 H USH990 H US H990H US 38637889 A US38637889 A US 38637889A US H990 H USH990 H US H990H
Authority
US
United States
Prior art keywords
nto
triazol
nitro
methylene chloride
temperature
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.)
Abandoned
Application number
US07/386,378
Inventor
Eleonore G. Kayser
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.)
US Department of Navy
Original Assignee
US Department of Navy
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
Application filed by US Department of Navy filed Critical US Department of Navy
Priority to US07/386,378 priority Critical patent/USH990H/en
Assigned to UNITED STATES OF AMERICA, THE, AS REPRESENTED BY THE DEPARTMENT OF THE NAVY reassignment UNITED STATES OF AMERICA, THE, AS REPRESENTED BY THE DEPARTMENT OF THE NAVY ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: KAYSER, ELEONORE G.
Application granted granted Critical
Publication of USH990H publication Critical patent/USH990H/en
Abandoned legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • C07D249/101,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D249/12Oxygen or sulfur atoms

Definitions

  • This invention relates to hetrocylic organic explosives and more particularly to nitrated tetrazoles.
  • NTO 3-nitro-1,2,4-triazol-5-one
  • an object of this invention is to provide a method of obtaining small particle size 3-nitro-1,2,4-triazol-5-one (NTO).
  • Another object of this invention is to provide NTO having a uniform particle size.
  • a further object of this invention is to provide NTO in a form suitable for use as a booster explosive material.
  • NTO finely divided 3-nitro-1,2,4-triazol-5-one
  • step (3) isolating the finely divided particles of 3-nitro-1,2,4-triazol-5-one (NTO) which are produced in step (2).
  • the large, jagged, needlelike 3-nitro-1,2,4-triazol-5-one (NTO) crystals are first dissolved in hot dimethylsulfoxide (DMSO).
  • DMSO dimethylsulfoxide
  • the hot DMSO is preferably at a temperature of from about 60° C. to about 90° C., and more preferable from 70° C. to 80° C.
  • the DMSO is preferably saturated with the NTO. At this time insoluble impurties may be removed by filtration.
  • a fine stream of the hot NTO/DMSO solution is injected into methylene chloride which is kept at a temperature of from about -10° C. to about 30° C. and more preferably from 0° C. to 25° C., and still more preferably at from 5° C. to 15° C.
  • the fine stream of NTO/DMSO is created by injecting the solution through an opening (e.g., jet or tube) having an internal diameter of 0.70 mm or less and preferably of 0.40 mm or less.
  • the lower limit on the diameter of the tube is determined by practical considerations such as what size tubing is available and at what rate the crystals are to be produced.
  • Another variation of this invention is to blow a stream of atomized NTO/DMSO solution in an inert gas (argon, helium nitrogen, etc.) into the methylene chloride. In this manner much smaller purer crystals of NTO will be produced.
  • an inert gas argon, helium nitrogen, etc.
  • NTO 3-nitro-1,2,4-triazol-5-one
  • DMSO hot dimethylsulfoxide
  • This NTO/DMSO solution was then injected through a No. 27 needle into 150 ml of methylene chloride at room temperature.
  • the NTO/DMSO/methylene chloride mixture was filtered and the collected solid was washed 3 times with approximately 100 ml of methylene chloride and filtered. The solid was dried under vacuum at approximately 50° C. to a constant weight.
  • This process increased the surface area of the NTO from 2,702 cm 2 /cm 3 to 56,742 cm 2 /cm 3 .
  • Blowing a stream of the atomized NTO/DMSO solution in an inert gas (nitrogen) into the methylene chloride increased the surface area of the NTO to 68,515 cm 2 /cm 3 .

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

The production of 3-nitro-1,2,4-triazol-5-one (NTO) having finely divided rticles of uniform size by dissolving conventionally produced large, jagged, rods of NTO in hot dimethylsulfoxide and then injecting the hot solution through a small orifice into methylene chloride at a temperature of from about -10° C. to about 30° C.

Description

BACKGROUND OF THE INVENTION
This invention relates to hetrocylic organic explosives and more particularly to nitrated tetrazoles.
3-nitro-1,2,4-triazol-5-one (NTO) is typically recrystallized in water. Unfortunately, NTO recrystallizes from water in relatively large, jagged rod-like particles that have a tendency to agglomerate. The irregular and jagged crystal shapes cause the mixing of the explosive formulations with NTO to be highly viscous and difficult to process and to pour. As a result, the amount of NTO which can be used in a processable explosive composition is limited and the performance of the explosive is therefore reduced.
SUMMARY OF THE INVENTION
Accordingly, an object of this invention is to provide a method of obtaining small particle size 3-nitro-1,2,4-triazol-5-one (NTO).
Another object of this invention is to provide NTO having a uniform particle size.
A further object of this invention is to provide NTO in a form suitable for use as a booster explosive material.
These and the other objects of this invention are accomplished by providing a process for producing finely divided 3-nitro-1,2,4-triazol-5-one (NTO) comprising:
(1) dissolving 3-nitro-1,2,4-triazol-5-one (NTO) in hot dimethylsulfoxide (DMSO);
(2) injecting the hot NTO/DMSO solution through an opening of 0.70 mm or less into methylene chlorine at room temperature; and
(3) isolating the finely divided particles of 3-nitro-1,2,4-triazol-5-one (NTO) which are produced in step (2).
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
In the present process the large, jagged, needlelike 3-nitro-1,2,4-triazol-5-one (NTO) crystals are first dissolved in hot dimethylsulfoxide (DMSO). The hot DMSO is preferably at a temperature of from about 60° C. to about 90° C., and more preferable from 70° C. to 80° C. The DMSO is preferably saturated with the NTO. At this time insoluble impurties may be removed by filtration.
Next a fine stream of the hot NTO/DMSO solution is injected into methylene chloride which is kept at a temperature of from about -10° C. to about 30° C. and more preferably from 0° C. to 25° C., and still more preferably at from 5° C. to 15° C. The fine stream of NTO/DMSO is created by injecting the solution through an opening (e.g., jet or tube) having an internal diameter of 0.70 mm or less and preferably of 0.40 mm or less. The lower limit on the diameter of the tube is determined by practical considerations such as what size tubing is available and at what rate the crystals are to be produced.
Another variation of this invention is to blow a stream of atomized NTO/DMSO solution in an inert gas (argon, helium nitrogen, etc.) into the methylene chloride. In this manner much smaller purer crystals of NTO will be produced.
The product crystals of NTO are then collected and washed with methylene chloride (or a similar solvent). Finally, the NTO is dried at from about 45° C. to about 55° C. under vacuum.
The general nature of the invention having been set forth, the following example is presented as specific example thereof. It will be understood that this invention is not limited to this specific example but is susceptible to various modifications that will be recognized by one of ordinary skill in the art.
EXAMPLE
Approximately 3.0 to 3.5 grams of large particle size (2,702 cm2 /cm3) 3-nitro-1,2,4-triazol-5-one (NTO) was dissolved in 4 to 5 ml of hot dimethylsulfoxide (DMSO) at a temperature of 70° C. This NTO/DMSO solution was then injected through a No. 27 needle into 150 ml of methylene chloride at room temperature. The NTO/DMSO/methylene chloride mixture was filtered and the collected solid was washed 3 times with approximately 100 ml of methylene chloride and filtered. The solid was dried under vacuum at approximately 50° C. to a constant weight. This process increased the surface area of the NTO from 2,702 cm2 /cm3 to 56,742 cm2 /cm3. Blowing a stream of the atomized NTO/DMSO solution in an inert gas (nitrogen) into the methylene chloride increased the surface area of the NTO to 68,515 cm2 /cm3.
Obviously, numerous modifications and variations of the present invention are possible in light of the above teachings. It is therefore to be understood that within the scope of the appended claims the invention may be practiced otherwise than as specifically described.

Claims (5)

What is claimed is:
1. A process for producing finely divided 3-nitro-1,2,4-triazol-5-one of uniform particle size comprising:
(1) dissolving conventional large, jagged, rodlike 3-nitro-1,2,4-triazol-5-one crystals having a particle size of (2,702 cm2 /cm3 in hot dimenthylsulfoxide at a temperature of from about 60° C. to about 90° C.;
(2) injecting the hot dimethylsulfoxide solution through an opening of 0.70 mm or less in diameter in methylene chloride which is kept at a temperature of from about -10° C. to about 30° C.; and
(3) isolating the finely divided particles of 3-nitro-1,2,4-triazol-5-one which are produced in step (2).
2. The process of claim 1 wherein the hot dimethylsulfoxide in step (1) is at a temperature of from 70° C. to 80° C.
3. The process of claim 1 wherein the methylene chloride in step (2) is maintained at a temperature of from 0° C. to 25° C.
4. The process of claim 3 wherein the methylene chloride in step (2) is maintained at a temperature of from 5° C. to 15° C.
5. The process of claim 1 wherein the opening in step (1) is 0.40 mm or less in diameter.
US07/386,378 1989-07-26 1989-07-26 Recrystallization of 3-nitro-1,2,4-triazol-5-one from dimethylsulfoxide and methylene chloride Abandoned USH990H (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US07/386,378 USH990H (en) 1989-07-26 1989-07-26 Recrystallization of 3-nitro-1,2,4-triazol-5-one from dimethylsulfoxide and methylene chloride

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US07/386,378 USH990H (en) 1989-07-26 1989-07-26 Recrystallization of 3-nitro-1,2,4-triazol-5-one from dimethylsulfoxide and methylene chloride

Publications (1)

Publication Number Publication Date
USH990H true USH990H (en) 1991-11-05

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
US07/386,378 Abandoned USH990H (en) 1989-07-26 1989-07-26 Recrystallization of 3-nitro-1,2,4-triazol-5-one from dimethylsulfoxide and methylene chloride

Country Status (1)

Country Link
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994006779A1 (en) * 1992-09-21 1994-03-31 Dynamit Nobel Aktiengesellschaft Nitrotriazolone for detonation purposes
FR2774983A1 (en) * 1998-02-18 1999-08-20 Poudres & Explosifs Ste Nale A new process for obtaining small spherical particles of 5-oxo-3-nitro 1,2,4-triazole (ONTA), used in pyrotechnic and explosive compositions
CN114315745A (en) * 2021-12-27 2022-04-12 中北大学 Nano-scale NTO crystal and preparation method thereof

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994006779A1 (en) * 1992-09-21 1994-03-31 Dynamit Nobel Aktiengesellschaft Nitrotriazolone for detonation purposes
FR2774983A1 (en) * 1998-02-18 1999-08-20 Poudres & Explosifs Ste Nale A new process for obtaining small spherical particles of 5-oxo-3-nitro 1,2,4-triazole (ONTA), used in pyrotechnic and explosive compositions
CN114315745A (en) * 2021-12-27 2022-04-12 中北大学 Nano-scale NTO crystal and preparation method thereof
CN114315745B (en) * 2021-12-27 2023-08-18 中北大学 Nanoscale NTO crystal and preparation method thereof

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Owner name: UNITED STATES OF AMERICA, THE, AS REPRESENTED BY T

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST.;ASSIGNOR:KAYSER, ELEONORE G.;REEL/FRAME:005132/0865

Effective date: 19890520

STCF Information on status: patent grant

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