Shortcut methods are a prerequisite for the fast evaluation of alternatives in process design. The rectification body method (RBM) for calculating the minimum energy demand of homogeneous, azeotropic multicomponent distillation processes is presented. The new method incorporates both the classical Underwood technique and certain preuiously proposed techniques as special cases. It employs all pinch point branches of both column sections and thus requires no a priori selection of active pinch points. It is entirely general and can be applied to any type of split of nonideal and azeotropic mixtures irrespective of the number of components. Hence, it significantly extends previous results and practical applicability. Its features are highlighted through examples of nonideal separations with three, four, and five components.
In conceptual process design many alternatives can arise for the separation of multicomponent
mixtures. Shortcut methods can be used to evaluate and compare all variants in a first step. In
this work shortcut methods for hybrid membrane/distillation processes are presented. The
distillation is addressed by the rectification body method recently developed by the authors,
providing the minimum energy demand of a separation and the optimal sidestream composition.
The membrane unit is evaluated using the minimum membrane area. It is a lower bound for
the actual membrane area and can be used to estimate the real membrane area and thus the
investment cost of the membrane process. The novel method overcomes limitations of previous
methods: It can be applied to multicomponent nonideal mixtures and to general flux laws for
any membrane. The stated methodology is applied to the purification of ethanol and to the
separation of the reactor output stream in methyl tert-butyl ether production.
An experimental study of ethanol dehydration with cyclohexane as
the entrainer has been carried
out in order to verify the existence of multiple steady states in
heterogeneous azeotropic
distillation. As a basis, the bifurcation diagram for the ethanol
product purity is determined
from thermodynamic considerations using the distillate flow rate as the
bifurcation parameter.
The predicted multiple steady states are then verified by rigorous
simulation and by experiments
on a laboratory tray column with a decanter. The hysteresis
behavior due to multiple steady
states is also verified in a dynamic experiment.
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