Mixtures of alkanes and ethanol are important in many
areas, for
example, as fuel blends. This paper describes new experimental data
obtained for the liquid–liquid equilibrium phase behavior of
normal alkanes (n-alkanes; C
n
H2n+2; 9 ≤ n ≤
24) with ethanol. The results were obtained by applying the cloud
point method in a temperature range of T = 230–423
K at ambient pressure. All systems are partially miscible with an
upper critical solution point. The two phase regions of the phase
diagrams show no indication of any obvious optical irregularities,
like birefringence, coloring, formation of schlieren, or remarkable
turbidity, except critical opalescence. With increasing length of
the molecular chain of the n-alkanes, the (liquid–liquid)
critical point is shifted to higher temperatures and higher ethanol
content. The data are analyzed numerically implying Ising criticality.
The nonsymmetric shape of the phase body is considered in different
approaches for describing the diameter by presuming (a) the validity
of the rectilinear diameter rule, (b) a nonlinear diameter predicted
in the theory of complete scaling, and (c) combining both concepts.
The numerical analysis yields the critical temperature, the critical
composition, the width, and the diameter of the phase diagrams. The
results are compared with literature data sets from similar mixtures;
these data are also evaluated in terms of the models applied here.
Phase diagrams of 13 different sets of mixtures are measured and analyzed
to extract general aspects of the behavior of the normal alkane–ethanol
mixtures. A simple Flory–Huggins-like approach allows a semiquantitative
description of the experimental results of the critical temperatures.
Therefore, it confirms the picture of molecular ordering within the
solutions.