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Order–disorder phase transitions in NH4Br x Cl1–x crystals
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16.The necessary values of the isothermal compressibility and thermal expansion coefficient are not known for the mixed crystals at high pressures. Thus, we have chosen to make no corrections for changes in length and density. The true values at high pressures can be obtained by multiplying the nominal values reported here by the factor A rough estimate, based on and in the disordered phase for all x, indicates that the systematic correction required at 250 K and 4 kbar is only and the change will be proportionally less at higher temperatures and lower pressures.
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26.As in Ref. 3, we have taken and have used and Near the triple point, and
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