A composite silica–divinylbenzene
(SiO2/DVB)
adsorbent was prepared for the adsorption of ethanol from the ethanol–water
mixture. Fourier transform infrared spectroscopy, X-ray diffraction,
scanning electron microscopy, and a Brunauer, Emmett and Teller surface
area analyzer were utilized for the characterization analysis of the
adsorbents. Batch experiments were executed at different initial ethanol
concentrations (10–95 vol %), contact times (1–24 h),
and temperatures (10–40 °C). The equilibrium studies indicated
a favorable adsorption of ethanol on SiO2/DVB because of
a separation factor R
l of 0.18 from the
Langmuir model. Moreover, Freundlich parameter constant n was found to be 2.37. This implies that the adsorption is governed
by a physical process. Results in the experimental data best-fitted
the pseudo-second-order kinetic model (R
2 ≥ 0.98 and RMSE ≤ 1.26), which suggests chemisorption
as the rate-limiting step of the adsorption system. Based on the Weber–Morris
kinetic analysis, intraparticle diffusion occurred after the outer
surface of the SiO2/DVB became saturated by ethanol molecules.
Approximately 99.2 ± 0.4% (20 °C) and 99.8 ± 0.2% (30
°C) of the ethanol were adsorbed onto the SiO2/DVB
adsorbent. Furthermore, thermodynamic parameters indicated a nonspontaneous
and exothermic reaction in the adsorption process. It was revealed
that the reusability profile of SiO2/DVB showed a 5.3%
reduction in terms of the adsorption capacity after the first cycle
and 8.3% reduction after four cycles.