Research articles
ScienceAsia 48 (2022):ID 804-812 |doi:
10.2306/scienceasia1513-1874.2022.121
Adsorption behavior and mechanism of alizarin yellow and
rhodamine B dyes on water hyacinth (Eichhornia crassipes)
leaves
Suchada Sawasdee*, Prachart Watcharabundit
ABSTRACT: This work studied a low-cost water hyacinth biosorbent to remove alizarin yellow (AY) and rhodamine
B (RB) from aqueous solutions. The physicochemical characterization of the water hyacinth leaf (WHL) was carried
out by Brunauer-Emmett-Teller surface area analysis, Fourier transform infrared spectroscopy, and scanning electron
microscopy. Contact time, pH, initial dye concentration, and temperature on adsorption were investigated in batch
mode. The maximum removal of AY and RB was detected at pH 2. The results showed that the adsorption of dyes
was enhanced with increased contact time, initial dye concentration, and temperature. The contact time reached
equilibrium within 120 min and 90 min for AY and RB, respectively. The Langmuir and Freundlich isotherm models
were applied to the equilibrium data. The Langmuir isotherm model better described the equilibrium data, indicating
the monolayer adsorption for all dyes. The maximum adsorption capacity values from the Langmuir model were 37.04
and 23.98 mg/g for AY and RB, respectively. The kinetic data of the adsorption were better described using the pseudosecond-order model. Thermodynamic studies showed that the adsorption of dyes was endothermic and spontaneous,
and the adsorption was physisorption. The adsorption mechanisms involved H-bonding, Yoshida H-bonding, n??, and
? ? ? interactions for both dyes. Moreover, electrostatic interactions could form between the negative parts of AY and
the positive surface of the water hyacinth leaf. In conclusion, the water hyacinth leaf could be employed as a low-cost
adsorbent to remove AY and RB from wastewater.
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Department of Chemistry, Thepsatri Rajabhat University, Lopburi 15000 Thailand |
* Corresponding author, E-mail: ps_neng@hotmail.com
Received 10 Jan 2022, Accepted 30 May 2022
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