The thermodynamics of mixed crystals of ammonium chloride and ammonium bromide. - III. The heat capacity from 8 to 300 K of solid solutions of composition NH 4 Br 0.20 Cl 0.80 and NH 4 Br 0.74 Cl 0.26

The heat capacity of the mixed crystals NH 4 Br 0.20 CI 0.80 and NH 4 Br 0.74 CI 0.26 has been measured from ca . 8 to 300 K. The first of these solids has, as expected, two gradual transitions, the lower having an entropy of transition ∆ S λ of 3.79 J K –1 mol –1 , and the upper a ∆ S λ of 4.51 J K –1 mol –1 . The heat capacity between these two transitions is always considerably above the ‘normal’ or baseline value, and it appears that the orientational disordering of the ammonium ions, while completed in the γ → β transition, commences in the δ-phase. The other, bromide-rich mixed crystal shows no sign of a δ → γ transition, but has a λ -type γ → β transition which culminates at 262.5 K, with ∆ S λ = 7.31 J K –1 mol –1 . The heat capacity of both mixed crystals in the β-phase, like that of the pure components, is ‘anomalously’ high, the additional heat capacity for the solid solutions being larger than that for the pure salts. The phase diagram for the ammonium-chloride–ammonium-bromide system is shown; it combines previous information with that provided by the heat-capacity results reported in this and previous papers.

The heat capacity C p of ammonium chloride, ammonium bromide and the mixed crystal NH 4 Br 0.55 Cl 0.45 has been analysed, for temperatures in the range 0-500 K, on the assumption that can be expressed as the sum of the terms ( C p — C v ), C (lat.), C (lib.), C (int.) and C (extra); C (lat.), C (lib.) and C (int.) are respectively, the contributions from the lattice vibrations (phonons), and the librations (torsional oscillations) and internal vibrations of the ammonium ions. C (extra) is the contribution from order-disorder changes or any other ‘abnormal’ sources. The analysis requires a knowledge of certain thermodynamic and spectroscopic properties of the crystals, and current information on these has been surveyed. The ‘normal ’ or ‘baseline’ heat capacity C´ p for the three solids has been estimated; C´ p is the molar heat capacity to be expected from the progressive excitation of the lattice vibrations, torsional oscillations and internal vibration of the cations, and from the expansion of the lattice. By comparing C´ p and the observed heat capacity C p , C (extra) has been evaluated, making it possible to examine the development with rising temperature of the configurational or otherwise ‘extra’ entropy. The main results emerging from this are the following, ( a ) For all three solids, the entropy gain at the λ-transition (or at the two lower transitions, taken together, in ammonium bromide) is not about R ln 2, as has often been stated, but is roughly 50 % larger. The excess over R ln 2 is to be attributed to changes in the phonon spectrum and to a reduction in the frequency of the torsional oscillations of the ammonium ions, ( b ) The heat capacity of the β-phase of all three solids is abnormally large. Possible reasons for this are briefly discussed, but a definitive explanation is lacking. ( c ) The overall entropy gain for all three solids when the high-temperature face-centred a-phase has been formed is considerably greater than R In 6, the configurational contribution to be expected from the structural evidence that each ammonium ion in this phase has access to six distinguishable orientations. The balance is believed to be due to enhanced freedom of torsional movement of the ammonium ions, which must be a complex motion. However, from its observable thermodynamic consequences, this motion is still far from true free rotation.


The heat capacity of a mixed crystal of ammonium chloride and ammonium bromide, of formula NH 4 Br, 0.55 Cl 0.45 , has been measured for temperatures in the range 8-300 K in one calorimeter, and 270K-476K in a second calorimeter. The mixed crystal undergoes a >.-type transition at T = 271.2K, and an essentially isothermal transition, to a facecentred cubic crystal, at 382.8 K. At this second transition, considerable superheating of the low-temperature form and supercooling of the hightemperature form can occur. Thermodynamic parameters for the mixed crystal are given at rounded temperatures.


1963 ◽  
Vol 8 (1) ◽  
pp. 26-27 ◽  
Author(s):  
Priscilla S. Costich ◽  
George J. Maass ◽  
Norman O. Smith

1984 ◽  
Vol 16 (8) ◽  
pp. 719-732 ◽  
Author(s):  
E.B. Amitin ◽  
O.A. Nabutovskaya ◽  
I.E. Paukov ◽  
K.S. Sukhovey

1965 ◽  
Vol 50 (2) ◽  
pp. 301-309 ◽  
Author(s):  
Jürg Müller

ABSTRACT An extract of human urine, which was previously shown to stimulate aldosterone production by rat adrenal sections, was further purified. Evidence was obtained that its aldosterone-stimulating effect was due to the presence of ammonium ions. Addition of ammonium chloride and of urine extract to the incubation medium caused identical increases in aldosterone production in vitro. In addition to ammonium ions, rubidium and caesium ions also stimulated aldosterone production up to 250% that of control values without a significant effect on corticosterone production. Similar dose-response curves were obtained when increasing concentrations of potassium, ammonium, rubidium and caesium ions were tested. Aldosterone production was maximal at concentrations of 7 mval/1 and was significantly lower at higher concentrations. When ammonium chloride and ACTH were simultaneously added to the incubation medium, the production of aldosterone and of corticosterone was lower than with ACTH alone. On the other hand, the stimulating activity on aldosterone and corticosterone production by »TPN« (NADP) and glucose-6-phosphate was enhanced by the simultaneous addition of ammonium chloride.


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