Pyridazinedione-based heterobicyclic covalent linkers and methods and applications thereof
US-2024425465-A1 · Dec 26, 2024 · US
US9512127B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9512127-B2 |
| Application number | US-201414499280-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 29, 2014 |
| Priority date | Sep 29, 2014 |
| Publication date | Dec 6, 2016 |
| Grant date | Dec 6, 2016 |
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A spherical morphology of the high explosive tetranitroglycoluril (TNGU) has been discovered. This new morphology exhibits approximately a twofold improvement in the response of the material to impact, more than a one and a half fold improvement in friction and the same high resistance to electrostatic discharge over non-spherical TNGU produced by other methods.
Opening claim text (preview).
What is claimed is: 1. A process for preparing an at least seventy percent (70%) yield of a spherical tetranitroglycoluril (TNGU) by recrystallization comprising the steps of: a) dissolving an amount of tetranitroglycoluril (TNGU) in a 100% solution of nitric acid (HNO 3 ) at a temperature of from about 20 to about 25 degrees Celsius to produce a homogeneous solution; b) stirring the solution while adding below the solution surface, from about 90 to about 100 milliters of a dichloromethane solvent; c) decanting the supernatant and re-suspending the TNGU in from about 20 to 30 milliliters of the dichloromethane solvent and allowing the precipitated spherical TNGU to settle; d) washing the precipitated spherical TNGU with from about 20 to 30 milliliters of the dichloromethane solvent four to six times until none of the nitric acid remains; and e) vacuum drying the resultant spherical TNGU and storing in a dessicator. 2. The process according to claim 1 wherein the spherical tetranitroglycoluril (TNGU) has a diameter of greater than 3 microns. 3. The process according to claim 1 wherein the spherical tetranitroglycoluril (TNGU) has a diameter of from greater than 3 microns to about 10 microns. 4. The process of claim 1 wherein the dichloromethane is added at a rate of about 1 milliliter per minute until the addition of dichloromethane is complete. 5. The process of claim 1 wherein the dichloromethane solvent is 100% dichloromethane. 6. The process of claim 1 wherein the temperature of the tetranitroglycoluril (TNGU) and nitric acid solution is 25 degrees Celsius.
Compositions or products which are defined by structure or arrangement of component of product (explosive charges of particular form or shape F42B1/00, F42B3/00) · CPC title
Ortho-condensed systems · CPC title
the compound being a nitrated acyclic, alicyclic or heterocyclic amine · CPC title
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