During
the production of ethylene sulfate (DTD) which is a novel
electrolyte additive in lithium-ion batteries, a lot of waste liquid
containing n-hexane, 1,2-dichloroethane, and DTD
was generated. DTD is separated from the mixture through a distillation
column and is poured into a crystallizer where the high purity product
is obtained by cooling and filtering, while the minimum boiling azeotrope
formed by n-hexane and 1,2-dichloroethane cannot
be separated by ordinary distillation methods. tert-Butyl acetate, sec-butyl acetate, and n-propyl acetate were selected as entrainers to separate the azeotrope
of n-hexane + 1,2-dichloroethane by extractive distillation
(ED). The binary interaction parameters (BIPs) of the thermodynamic
model are the key parameters used for the conceptual design. The BIPs
for the binary systems of 1,2-dichloroethane + sec-butyl acetate/n-propyl acetate/tert-butyl acetate have been reported in a previous work. In this work,
the vapor–liquid equilibrium (VLE) data for four binary systems
(n-hexane + 1,2-dichloroethane/tert-butyl acetate/sec-butyl acetate/n-propyl acetate) were determined at 101.3 kPa using an Ellis vapor–liquid
equilibrium device, and the thermodynamic consistency of experimental
data was tested by the Fredenslund test and Van Ness test. The VLE
data were used for regression of the BIPs of the nonrandom two-liquid
(NRTL), universal quasi-chemical (UNIQUAC), and Wilson activity coefficient
models.