TY - JOUR
T1 - Effective sequestration of tetracycline and ciprofloxacin from aqueous solutions by Al-based metal organic framework and reduced graphene oxide immobilized alginate biosorbents
AU - Kim, Nahyun
AU - Cha, Byungjun
AU - Yea, Yeonji
AU - Njaramba, Lewis Kamande
AU - Vigneshwaran, Sivakumar
AU - Elanchezhiyan, S. SD
AU - Park, Chang Min
N1 - Publisher Copyright:
© 2022 Elsevier B.V.
PY - 2022/12/15
Y1 - 2022/12/15
N2 - Antibiotics are chemical compounds commonly used to treat bacterial infections in humans and animals and can easily enter aquatic environments as a result of human activities. Tetracycline (TC) and ciprofloxacin (CIP) are two of the most common antibiotics found in water bodies. Aluminium-based metal organic framework (MOF) and reduced graphene oxide (rGO) were used as supporting materials in Alg hydrogel beads (Alg@MOF-rGO) in batch and column experiments to enhance the removal efficiency of TC and CIP. The as-prepared Alg@MOF-rGO hydrogel beads were effective in eliminating pharmaceutical residues from aquatic media. The physicochemical properties of the hydrogel were thoroughly characterized, and various key parameters, such as contact time, solution pH, adsorbent dose, temperature, co-existing ions, and different flow rates were studied to determine the maximum adsorption efficiency of the prepared hydrogel beads. The Alg@MOF-rGO beads showed the highest adsorption capacity to eliminate TC and CIP (qm = 43.76 and 40.76 mg/g for TC and CIP, respectively) during reaction time of 12 h compared to the other forms of hydrogel beads, and the adsorption of TC and CIP followed the Langmuir isotherm and pseudo-second-order (PSO) kinetic models. According to the pH and temperature study, the maximum adsorption capacity were attained at neutral pH (pH 7) and temperature of 40 °C. The continuous column studies showed that the Thomas, Adams-Bohart, and Yoon-Nelson models fit well for eliminating TC and CIP on the prepared Alg@MOF-rGO beads. Several attractive forces such as electrostatic interaction, pore filling, hydrogen bonding, and π-π attraction were the major forces responsible for the uptake of TC and CIP on Alg@MOF-rGO beads from the aquatic environment.
AB - Antibiotics are chemical compounds commonly used to treat bacterial infections in humans and animals and can easily enter aquatic environments as a result of human activities. Tetracycline (TC) and ciprofloxacin (CIP) are two of the most common antibiotics found in water bodies. Aluminium-based metal organic framework (MOF) and reduced graphene oxide (rGO) were used as supporting materials in Alg hydrogel beads (Alg@MOF-rGO) in batch and column experiments to enhance the removal efficiency of TC and CIP. The as-prepared Alg@MOF-rGO hydrogel beads were effective in eliminating pharmaceutical residues from aquatic media. The physicochemical properties of the hydrogel were thoroughly characterized, and various key parameters, such as contact time, solution pH, adsorbent dose, temperature, co-existing ions, and different flow rates were studied to determine the maximum adsorption efficiency of the prepared hydrogel beads. The Alg@MOF-rGO beads showed the highest adsorption capacity to eliminate TC and CIP (qm = 43.76 and 40.76 mg/g for TC and CIP, respectively) during reaction time of 12 h compared to the other forms of hydrogel beads, and the adsorption of TC and CIP followed the Langmuir isotherm and pseudo-second-order (PSO) kinetic models. According to the pH and temperature study, the maximum adsorption capacity were attained at neutral pH (pH 7) and temperature of 40 °C. The continuous column studies showed that the Thomas, Adams-Bohart, and Yoon-Nelson models fit well for eliminating TC and CIP on the prepared Alg@MOF-rGO beads. Several attractive forces such as electrostatic interaction, pore filling, hydrogen bonding, and π-π attraction were the major forces responsible for the uptake of TC and CIP on Alg@MOF-rGO beads from the aquatic environment.
KW - Alginate
KW - Ciprofloxacin
KW - MOF
KW - rGO
KW - Tetracycline
UR - http://www.scopus.com/inward/record.url?scp=85135717057&partnerID=8YFLogxK
U2 - 10.1016/j.cej.2022.138068
DO - 10.1016/j.cej.2022.138068
M3 - Article
AN - SCOPUS:85135717057
SN - 1385-8947
VL - 450
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 138068
ER -