METHOD FOR PURIFYING BORAZANE

Abstract

A method for purifying solid borazane (NH.sub.3BH.sub.3 (s)) includes a) bringing solid borazane (NH.sub.3BH.sub.3 (s)) containing impurities into contact with a stream of gaseous ammonia (NH.sub.3 (g)) to obtain, by selective liquefaction of the borazane, a liquid phase containing liquefied borazane and ammonia and a solid phase constituted of at least a part of the impurities, b) separating the liquid and solid phases for recovery of the liquid phase, on the one hand, and of the solid phase, on the other hand; c) removing the ammonia from the recovered liquid phase, this removal causing precipitation of the purified borazane (NH.sub.3BH.sub.3 (s)); and d) recovering the purified precipitated borazane (NH.sub.3BH.sub.3 (s)).

Claims

1. A method for purifying solid borazane (NH.sub.3BH.sub.3 (s)) containing impurities, said method comprising: a) bringing solid borazane (NH.sub.3BH.sub.3 (s)) containing impurities into contact with a stream of gaseous ammonia (NH.sub.3 (g)) to obtain, by selective liquefaction of the borazane, a liquid phase containing liquefied borazane and ammonia and a solid phase constituted of at least a part of said impurities; b) separating said liquid and solid phases for recovery of said liquid phase, on the one hand, and of said solid phase, on the other hand; c) removing the ammonia from said recovered liquid phase, the removal causing precipitation of the purified borazane (NH.sub.3BH.sub.3 (s)); and d) recovering said purified precipitated borazane (NH.sub.3BH.sub.3 (s)).

2. The method as claimed in claim 1, wherein it is performed at atmospheric pressure and at room temperature.

3. The method as claimed in claim 1, wherein it is performed continuously.

4. The method as claimed in claims 1, wherein said solid borazane (NH.sub.3BH.sub.3 (s)) is in dispersed form or in undispersed form.

5. The method as claimed in claims 1, wherein the gaseous ammonia (NH.sub.3 (g)) is used in a gaseous ammonia/solid borazane mole ratio (R=NH.sub.3 (g)/NH.sub.3BH.sub.3 (s)) of greater than 1.

6. The method as claimed in claim 1, wherein the separation of the liquid and solid phases is performed by filtration or by centrifugation.

7. The method as claimed in claim 1, wherein the ammonia is removed from said recovered liquid phase by evaporation.

8. The method as claimed in claim 1, wherein said separation is performed on conclusion of said bringing into contact, after stopping said stream.

9. The method as claimed in claim 1, wherein said separation is performed during said bringing into contact.

10. The method as claimed in claim 9, wherein said solid borazane (NH.sub.3BH.sub.3 (s)), placed on a filter, is brought into contact with a stream of ammonia gas (NH.sub.3 (g)) and wherein the liquid phase generated is recovered below said filter whereas the solid phase is retained by said filter.

11. The method as claimed in claim 1, wherein the gaseous ammonia (NH.sub.3 (g)) is used in a gaseous ammonia/solid borazane (R=NH.sub.3 (g)/NH.sub.3BH.sub.3 (s)) mole ratio between 5 and 15.

12. The method as claimed in claim 6, wherein the separation of the liquid and solid phases is performed by filtration.

Description

[0043] It is proposed below to specify one and the other of said implementation variants of the method of the invention with reference to the attached FIGS. 1A to 2C).

[0044] FIGS. 1A, 1B, 1C and 1D illustrate a first implementation variant of the borazane purification method according to the invention (=the first variant specified above), more specifically a first implementation variant according to which it is on conclusion of the bringing of the solid borazane into contact with a stream of gaseous ammonia (FIG. 1B) that the separation of the liquid and solid phases takes place.

[0045] FIGS. 2A, 2B and 2C illustrate a second implementation variant of the borazane purification method according to the invention (=the second variant specified above), more specifically a second implementation variant according to which the separation of the liquid and solid phases is performed during the bringing of the solid borazane into contact with a stream of gaseous ammonia (FIG. 2B).

[0046] FIGS. 3A and 3B show, respectively, the .sup.1H NMR spectra (solvent: D.sub.2O) of borazane before (FIG. 3A) and after (FIG. 3B) purification according to the example of the invention (see below); FIGS. 4A and 4B show, respectively, the .sup.11B NMR spectra (solvent: D.sub.2O) of borazane before (FIG. 4A) and after (FIG. 4B) purification according to the example of the invention (see below).

[0047] FIG. 1A thus schematically represents a bringing into contact of solid borazane (NH.sub.3BH.sub.3 (s))/stream of gaseous ammonia (NH.sub.3 (g)). The solid borazane is dispersed at the bottom of a round-bottomed flask. A stream of gaseous ammonia (NH.sub.3 (g)) passes through said flask.

[0048] FIG. 1B schematically represents the result obtained: the solid borazane has been liquefied. Solid impurities S are present within the liquid phase L obtained.

[0049] After stopping the stream of ammonia, there is no difficulty in separating the liquid L and solid S phases. The liquid phase L is obtained freed of the solid impurities S (FIG. 1C).

[0050] FIG. 1D shows the removal of ammonia (by placing the flask containing the liquid phase L under vacuum; said placing under vacuum is represented schematically by the arrow V). Said FIG. 1D in fact shows the content of the flask at the end of said placing under vacuum V, i.e. the purified borazane obtained, referenced NH.sub.3BH.sub.3 (s).

[0051] FIG. 2A shows:

[0052] at 1, a Schlenk tube,

[0053] at 2, a filter,

[0054] at 3, a three-necked round-bottomed flask, and

[0055] at 4, a neck of said three-necked round-bottomed flask.

[0056] The arrows symbolize the stream of gaseous ammonia (NH.sub.3 (g)) placed in circulation.

[0057] The solid borazane (NH.sub.3BH.sub.3 (s)) to be purified is placed on said filter 2.

[0058] On contact with the stream of gaseous ammonia (NH.sub.3 (g)), said solid borazane (NH.sub.3BH.sub.3 (s)) becomes liquefied; once liquefied (co-liquefied with gaseous ammonia), it passes through said filter 2 and becomes accumulated at the bottom of the flask 3. The solid phase S is stopped by said filter 2. This (steps a) and b) of the method of the invention) is represented schematically in FIG. 2B.

[0059] When all the solid borazane has been liquefied, the stream of gaseous ammonia is stopped. Removal of the ammonia by placing the volume of the flask 3 under vacuum is then performed. This placing under vacuum is represented schematically, in FIG. 2C, by the arrow V. FIG. 2C in fact shows the contents of the flask 3 at the end of said placing under vacuum V. The solid borazane (NH.sub.3BH.sub.3 (s)) initially placed on the filter 2 is obtained freed of the solid phase S, i.e. purified. It has been referenced NH.sub.3BH.sub.3 (s).

[0060] The method of the invention, more specifically its second variant, as specified above, is illustrated by the example below.

EXAMPLE

[0061] A device, as represented schematically in FIGS. 2A and 2B, comprising a Schlenk tube (4 cm in diameter) equipped with a filter and connected to a three-necked round-bottomed flask was used.

[0062] Ammonia borane (or borazane) in powder form (about 4 g) was placed on the filter and a stream of gaseous ammonia (about 45 mL/min) was passed through the bed of powder and said filter (in the direction: upstream to downstream of the filter), at room temperature (20 C.) and at atmospheric pressure. Under these conditions, the ammonia borane was (co-)liquefied and, by sedimentation, the liquid phase generated passed through the filter. The insoluble impurities in said liquid phase remained on the filter.

[0063] After 2 hours of filtration under ammonia, the filtered liquid phase was recovered and dried in ambient air (natural evaporation of the ammonia) to obtain the purified ammonia borane in solid form (FIG. 2C). 3.89 g of purified ammonia borane were thus recovered.

[0064] The efficiency of the purification was evaluated by analyzing the melting point of the ammonia borane by DSC (Differential Scanning calorimetry) analysis, performed with a temperature increase ramp of 5 C./min. Before purification according to the invention, the melting point of the product was 112.8 C.; after purification according to the invention, it was 115.9 C. This increase in melting point reflects an improvement in the purity of the product.

[0065] Comparative examination of the .sup.1H NMR and .sup.11B NMR spectra of the borazane used in said example, before and after purification according to the invention, is moreover proposed (see, respectively, FIGS. 3A and 3B and FIGS. 4A and 4B). It is clearly shown that peaks, undoubtedly corresponding to impurities (see the relative amounts relative to the peaks corresponding to the hydrogen atoms or to the boron atoms of borazane), present in the spectra of the borazane to be purified, are no longer present in the spectra of the purified borazane.