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Vaporization thermodynamics of K2S and K2SO3

The vaporization reactions, vapor pressures, and thermodynamics of potassium sulfide and potassium sulfite were studied for purposes of providing fundamental data for the seed cycle in magnetohydrodynamic electric power generation. Rate of effusion studies, supported by tube furnace experiments, X-ray powder diffraction, mass spectrometry and appropriate chemical analyses and tests, revealed that potassium sulfite disproportionates at high temperatures to form potassium sulfide and potassium sulfate. Potassium sulfide was observed to vaporize incongruently, the initial vapors beng predominantly potassium atoms, with minor species being S2 and various K-S molecules. The ratio of K/S2 in the vapor is very large initially and decreases steadily with prolonged heating. Several materials were evaluated for purposes of containing K2S/K2SO3 at temperatures or = 800 C: Pt, Mo, W, quartz, machinable glass, BN, high density graphite, pyrolytic coated graphite, and alumina. Of these, only alumina was observed to be chemically inert to both K2S but reacted with K2SO3. The other materials were not suitable for either substance. Thermodynamic calculations based on measured vapor pressures and approximate free energy functions are described. Results from isothermal total mass loss experiments and from thermogravimetric experiments are also included.

Bennet, J. E.↗

Thermodynamics of the potassium-sulfur-oxygen and related systems

The chemical reactions which occur when potassium sulfide, K2S, and potassium sulfite, K2SO3, are heated at temperatures where their vapor pressures are significant, were studied and the vapor pressures and the partial pressures of the chemical products were measured. Mass spectrometry of the vapor of potassium sulfide revealed only K(g). X-ray studies of the solid residues from vaporization experiments revealed K2S2(s) and chemical analyses of the same solid residues showed that the residues approached a composition K2Sx with x in the range 3-4. Vapor pressure of K2S was measured by simultaneous Knudsen-effusion and torsion-effusion (SKETE) in crucibles of aluminum oxide and of graphite. In each such experiment, the vapor pressures agreed initially, but then the apparent pressure by Knudsen-effusion increased suddenly and remained much greater than that by torsion-effusion for the remainder of the experiment. Results of third-law analysis of the torsion pressures imply a delta H (298K) of formation of K2S(s) of -364 + or - 12 kJ/mol. Vapor pressures over K2SO3(s) were measured by simultaneous Knudsen and torsion-effusion and by mass spectrometry. The vapor pressures of both K2S2O5(s) and K2SO3(s) were nonreproducible at a given temperature due to the vaporization reactions of the materials being irreversible under conditions in effusion cells.

Edwards, J. G.↗

Preliminary evaluation of the role of K2S in MHD hot stream seed recovery

Results are presented for recent analytical and experimental studies of the role of K2S in MHD hot stream seed recovery. The existing thermodynamic data base was found to contain large uncertainties and to be nonexistent for vapor phase K2S. Knudsen cell mass spectrometric experiments were undertaken to determine the vapor species in equilibrium with K2S(c). K atoms and S2 molecules ere found to be the major vapor phase species in vacuum, accounting for greater than 99 percent of the vapor phase. Combustion gas deposition studies using No. 2 Diesel fuel were also undertaken and revealed that condensed phase K2SO3 may potentially be an important compound in the MHD stream at near-stoichiometric combustion.

Bennett, J. E.↗