I want to make an azeotropic mixture of HCl and water from concentrated HCl.
2.
Azeotropic mixtures on the other hand have constant properties at their azeotropic composition and behave like pure components.
3.
Bernot " et al . " described the structure and properties of residue curve maps for ternary heterogeneous azeotropic mixtures.
4.
If zeotropic blends are used, it is common to select mixtures with small separation factors ( so called near-azeotropic mixtures ).
5.
What would happen to the concentration if I made the starting concentration greater than that of the azeotropic mixture and then boiled?
6.
A classic example to be cited here is the separation of an azeotropic mixture of benzene and cyclohexane, where aniline is one suitable solvent.
7.
Pressure-swing distillation is essentially the same as the unidirectional distillation used to break azeotropic mixtures, but here both positive and negative pressures may be employed.
8.
I suppose I can do this simply by diluting the HCl to the concentration of the azeotropic mixture ( which I think is 6.102M ).
9.
Azeotropic mixtures show a pressure maximum / temperature minimum or pressure minimum / temperature maximum that is above / below the values of the pure components.
10.
Because distillation cannot separate the constituents of an azeotrope, the separation of azeotropic mixtures ( also called " azeotrope breaking " ) is a topic of considerable interest.
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