A method for preparing libh4 xnh3 compound
A compound and product technology, applied in the field of material preparation, can solve problems such as low economic benefits and fossil fuel pollution, and achieve the effects of low equipment requirements, convenient synthesis, and simple process
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Embodiment 1
[0035] Embodiment 1 prepares LiBH 4 ·NH 3
[0036] At room temperature 25°C, 1g LiBH 4 Put it into a Schlenk test tube under argon gas. After vacuuming the test tube, slowly introduce ammonia gas. Stop feeding ammonia gas when it reaches 0.8 atm. After 20 minutes of reaction, pump the test tube to a vacuum state, and stop after 3 hours of vacuum. Reaction, the product is taken out in argon, which is mainly LiBH 4 ·NH 3 ( figure 1 Be the XRD spectrogram of gained product; figure 2 is the thermal analysis spectrum of the product).
Embodiment 2
[0037] Embodiment 2 prepares LiBH 4 2NH 3
[0038] At room temperature 25°C, 1g LiBH 4 Put it into a Schlenk test tube in argon, vacuumize the test tube, slowly feed ammonia gas, stop feeding ammonia gas when it reaches 0.8 atm, and take out the product in argon gas after reacting for 30 minutes, which is mainly LiBH 4 2NH 3 ( image 3 IR spectrogram for the resulting product; Figure 4 is the thermal analysis spectrum of the product).
Embodiment 3
[0039] Embodiment 3 prepares LiBH 4 ·3NH 3
[0040] At room temperature 25°C, 1g LiBH 4 Put it into a Schlenk test tube in argon, vacuumize the test tube, then slowly feed ammonia gas, stop feeding ammonia gas when it reaches 0.8 atm, react for 30 minutes and spread the liquid product along the tube wall, and the liquid is completely transformed into After the solid was left to stand for 30 minutes, it was taken out in argon, which was mainly LiBH 4 ·3NH 3 .
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