Displacement reaction for producing NF.sub.4 PF.sub.6

Abstract

A method of producing NF.sub.4 PF.sub.6 by a displacement reaction between NF.sub.4 BF.sub.4 and PF.sub.5.

Description

BACKGROUND OF THE INVENTION

1. Field of the Invention

This invention relates to methods of producing compositions and is particularly directed to a method of producing NF.sub.4 PF.sub.6 by a displacement reaction between NF.sub.4 BF.sub.4 and PF.sub.5.

2. Description of the Prior Art

NF.sub.4.sup.+ salts are the key ingredients for solid propellant NF.sub.3 --F.sub.2 gas generators, such as that disclosed by D. Pilipovich in U.S. Pat. No. 3,963,542, for chemical HF-DF lasers. Whereas NF.sub.4 SbF.sub.6 and NF.sub.4 AsF.sub.6 can be prepared with relative ease, according to the methods taught by W. E. Tolberg et al, in U.S. Pat. No. 3,708,570, and K. O. Christe et al, in U.S. Pat. No. 3,503,719, these compounds suffer from the disadvantage of containing a relatively heavy anion, thus decreasing their performance in an NF.sub.3 --F.sub.2 gas generator. This disadvantage can be overcome by replacing the SbF.sub.6.sup.- or AsF.sub.6.sup.- anion by the lighter PF.sub.6.sup.- anion. The existence of this salt has previously been claimed by Tolbert et al in U. S. Pat. No. 3,708,570, but their production process was so inefficient that they could not isolate an amount of material sufficient for its isolation, identification and characterization.

BRIEF SUMMARY AND OBJECTS OF THE INVENTION

This problem of synthesizing NF.sub.4 PF.sub.6 is overcome by the present invention. The method of the present invention involves a displacement reaction between the readily available NF.sub.4 BF.sub.4 and PF.sub.5 according to:

NF.sub.4 BF.sub.4 +PF.sub.5 .fwdarw.NF.sub.4 PF.sub.6 +BF.sub.3 applicants have found that the displacement reaction can be carried out at any temperature above the melting point of PF.sub.5 (-94.degree. C.) and below the decomposition temperature of NF.sub.4 PF.sub.6 (above 245.degree. C.). Moreover, the pressure is not essential and is given by the reaction temperature (that is, the vapor pressure of PF.sub.5).

This method provides NF.sub.4 PF.sub.6 of high purity.

Accordingly, it is an object of the present invention to provide an improved process for the production of NF.sub.4 PF.sub.6.

This and other objects and features of the present invention will be apparent from the following examples.

DETAILED DESCRIPTION OF THE INVENTION

In a typical experiment, pure NF.sub.4 BF.sub.4 (2.07 mmol) was combined at -196.degree. C. with an excess of PF.sub.5 (40.01 mmol) in a 10-ml 316 stainless steel cylinder. The mixture was kept at 25.degree. C. for 64 h. The volatile materials were removed in vacuo and separated by fractional condensation. They consisted of BF.sub.3 (2.05 mmol) and unreacted PF.sub.5 (37.93 mmol). The white solid residue had gained 120 mg in weight. Based on the above material balance, the conversion of NF.sub.4 BF.sub.4 to NF.sub.4 PF.sub.6 was essentially complete. This was further confirmed by vibrational spectroscopy which showed the solid to be NF.sub.4 PF.sub.6 containing no detectable amounts of NF.sub.4 BF.sub.4.

The salt NF.sub.4 PF.sub.6 is a white, crystalline, hydroscopic solid, stable at room temperature, but rapidly decomposing at 245.degree. C. Its characteristic x-ray diffraction powder pattern is listed in Table I. Its vibrational spectrum is listed in Table II and establishes the ionic nature of the salt, i.e. the presence of discrete NF.sub.4.sup.+ cations and PF.sub.6.sup.- anions. This was further confirmed by .sup.19 F nmr spectroscopy in HF solution which showed the triplet (J.sub.NF =230 Hz at .phi.=-217) characteristic for NF.sub.4.sup.+.

TABLE I______________________________________X-RAY POWDER DATA FOR NF.sub.4 PF.sub.6.sup.ad obsd d calcd Int h k l______________________________________5.40 5.36 ms 1 1 04.55 4.53 s 1 0 13.91 3.89 vs 1 1 13.79 3.79 s 2 0 02.91 2.91 ms 2112.65 2.65 m 1 0 22.40 2.40 vw 3 1 02.307 2.305 m 3 0 12.204 2.205 vw 3 1 12.171 2.171 mw 2 1 21.882 1.883 ms 3 0 2,0 0 31.825 1.827 vw 3 1 2,1 0 31.784 1.785 w 3 3 01.747 1.747 mw 4 1 11.685 1.685 w 3 2 2,2 0 31.646 1.646 w 2 1 31.622 1.622 w 4 2 11.536 1.540 vw 4 1 21.485 1.486 vw 5 1 01.464 1.463 vw 5 0 11.437 1.437 w 5 1 11.408 1.407 vw 5 2 01.365 1.365 vw 5 2 1,1 1 41.333 1.335 w 5 0 21.318 1.319 vw 4 4 01.302 1.304 vw 2 1 41.259 1.259 w 4 2 31.214 1.216 w 6 1 1______________________________________ .sup.a Tetragonal, a = 7.577, c = 5.653A, Cu K.sub..alpha. radiation Ni filter TABLE II______________________________________VIBRATIONAL SPECTRUM OF NF.sub.4 PF.sub.6Obsd Frequency (cm.sup.-1)Ir Raman Assignments for NF.sub.4.sup.+ (T.sub.d)______________________________________2380 vw 2.nu..sub.3 (A.sub.1 + E + F.sub.2) = 23202320 w2005 w .nu..sub.1 + .nu..sub.3 (F.sub.2) = 20081765 w .nu..sub.3 + .nu..sub.4 (A.sub.1 + E + F.sub.2) = 17691457 w .nu..sub.1 + .nu..sub.4 (F.sub.2) = 14571221 mw 2.nu..sub.4 (A.sub.1 + E + F.sub.2) = 12181166 vs 1168(1.5) .nu..sub.3 (F.sub.2) 1150(0.8)1135 vw1056 vw .nu..sub.2 + .nu..sub.4 (F.sub.1 + F.sub.2) = 1049 880(0.2) 2.nu..sub.2 (A.sub.1 + A.sub.2 + E) = 880 849(8.2) .nu..sub.1 (A.sub.1) 611 m 609(7.4) .nu..sub.4 (F.sub.2) 608 m 441(2.9) .nu..sub.2 (E)______________________________________ Assignments for PF.sub.6.sup.- (O.sub.h)______________________________________1590 w .nu..sub.1 + .nu..sub.3 (F.sub.1u) = 15901414 w .nu..sub.2 + .nu..sub.3 (F.sub.1u + F.sub.2u) = 14131308 vw .nu..sub.1 + .nu..sub.4 (F.sub.1u) = 1307 842 vs 838(1.5) .nu..sub.3 (F.sub.1u) 789 w 749 w 748(10) .nu..sub.1 (A.sub.1g) 571(0.8) .nu..sub.2 (E.sub.g) 559 s .nu..sub.4 (F.sub.1u) 474 vw 469(1.2) .nu..sub.5 (F.sub.2g)______________________________________

Obviously, numerous variations and modifications may be made without departing from the present invention. Accordingly, it should be clearly understood that the form of the present invention described above is illustrative only and is not intended to limit the scope of the present invention.

Claims

1. A process for the production of NF.sub.4 PF.sub.6 characterized by combining NF.sub.4 BF.sub.4 with an excess of PF.sub.5 at above about -196.degree. C., reacting the reactants while warming the reaction system to a temperature less than about 25.degree. C. and removing the volatile reaction products by pumping.