Spherical NTO crystal and preparation method thereof
A technology of crystal and volume ratio, which is applied in the direction of organic chemical methods, offensive equipment, and a single substance as explosives. It can solve the problems of low charge density, poor molding performance of mixed explosives, and restrictions on the use of NTO.
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[0030] The present invention provides a kind of preparation method of NTO crystal, comprises the following steps:
[0031] Dissolving NTO in a mixed solvent of dimethyl sulfoxide and water to obtain a saturated solution; the volume ratio of the dimethyl sulfoxide to water is 0.5-1.75:1, and the temperature of the saturated solution is 64-76°C ;
[0032] The saturated solution is cooled to crystallize, and the NTO crystals are precipitated; the cooling rate of the cooled crystallization is 3.0-4.5°C·min -1 ; The cooling crystallization is accompanied by stirring, and the stirring speed is 300-800r / min.
[0033] In the present invention, NTO is dissolved in a mixed solvent of dimethyl sulfoxide and water to obtain a saturated solution; the volume ratio of the dimethyl sulfoxide to water is 0.5 to 1.75:1, and the temperature of the saturated solution is 64 to 76°C. The present invention has no special limitation on the source of the NTO, and conventional commercially available...
Embodiment 1
[0047] The temperature of the double-layer jacketed reactor was adjusted to 70 ° C by means of external circulation temperature control; using the double-layer reactor as a container, 8 g of NTO was dissolved in 20 mL of a mixed solvent consisting of 12 mL of dimethyl sulfoxide and 8 mL of water. To obtain a saturated solution, keep warm for 30min;
[0048] Control the external circulation device of the reactor to make the reactor follow the temperature of 3.5°C·min -1 The cooling rate is lowered to 5°C; the cooling is accompanied by stirring at a speed of 500r / min; after cooling down to 5°C, continue to stir for 60 minutes;
[0049] The suspension obtained after stirring was subjected to suction filtration, washed with a saturated solution, and the filter residue obtained by suction filtration was freeze-dried at -84° C. for 240 min to obtain NTO crystals. The yield of the prepared NTO crystals was 80%.
[0050] The NTO crystal prepared in Example 1 is subjected to scanning...
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