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Evaluation of deep eutectic solvent as a new monomer for molecularly imprinted polymers for removal of bisphenol A

Deep eutectic solvent molecularly imprinted polymer (DES-MIP) was synthesized by bulk polymerization via free radical polymerization using bisphenol A (BPA) as a template, DES as a functional monomer, ethylene glycol dimethyl acrylate (EGDMA) as a crosslinker and benzoyl peroxide as initiator. DES f...

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Published in:Journal of polymer research 2023-06, Vol.30 (6), Article 205
Main Authors: Shah, Syed Asim Hussain, Asman, Saliza
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description Deep eutectic solvent molecularly imprinted polymer (DES-MIP) was synthesized by bulk polymerization via free radical polymerization using bisphenol A (BPA) as a template, DES as a functional monomer, ethylene glycol dimethyl acrylate (EGDMA) as a crosslinker and benzoyl peroxide as initiator. DES functional monomer was prepared by the combination of choline chloride methacrylic acid (ChCl-MAA). The synthesized DES-MIP was then compared with conventional molecularly imprinted polymer (MIP) synthesized using methacrylic acid (MAA) as a functional monomer. The DES-MIP has a higher selectivity for BPA (17.72 mg/g) than competing chemicals, including bisphenol AP (9.78 mg/g), 2-naphthol (8.25), and 4-tertiary butyl-phenol (6.98 mg/g). The optimization parameters include the effects of pH, adsorption kinetics, adsorption isotherm, and thermodynamic studies were investigated. DES-MIP showed the highest binding capacity at pH 7. The kinetic and isotherm studies demonstrated good agreement with a pseudo-second-order kinetic model and Langmuir isotherm models, respectively. The thermodynamic study proved that the adsorption of BPA on DES-MIP was exothermic and spontaneous with ΔH 0 (-23.734 × kJ/mol) and ΔG 0 (-2.929 kJ/mol − ). Reusability experiments show that the DES-MIP can be recycled five times without significantly diminishing its adsorption capacity. As a result, it proved that the contribution of DES as a functional monomer alternative in MIP synthesis considerably improved the recognition of BPA adsorption.
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DES functional monomer was prepared by the combination of choline chloride methacrylic acid (ChCl-MAA). The synthesized DES-MIP was then compared with conventional molecularly imprinted polymer (MIP) synthesized using methacrylic acid (MAA) as a functional monomer. The DES-MIP has a higher selectivity for BPA (17.72 mg/g) than competing chemicals, including bisphenol AP (9.78 mg/g), 2-naphthol (8.25), and 4-tertiary butyl-phenol (6.98 mg/g). The optimization parameters include the effects of pH, adsorption kinetics, adsorption isotherm, and thermodynamic studies were investigated. DES-MIP showed the highest binding capacity at pH 7. The kinetic and isotherm studies demonstrated good agreement with a pseudo-second-order kinetic model and Langmuir isotherm models, respectively. The thermodynamic study proved that the adsorption of BPA on DES-MIP was exothermic and spontaneous with ΔH 0 (-23.734 × kJ/mol) and ΔG 0 (-2.929 kJ/mol − ). Reusability experiments show that the DES-MIP can be recycled five times without significantly diminishing its adsorption capacity. 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DES functional monomer was prepared by the combination of choline chloride methacrylic acid (ChCl-MAA). The synthesized DES-MIP was then compared with conventional molecularly imprinted polymer (MIP) synthesized using methacrylic acid (MAA) as a functional monomer. The DES-MIP has a higher selectivity for BPA (17.72 mg/g) than competing chemicals, including bisphenol AP (9.78 mg/g), 2-naphthol (8.25), and 4-tertiary butyl-phenol (6.98 mg/g). The optimization parameters include the effects of pH, adsorption kinetics, adsorption isotherm, and thermodynamic studies were investigated. DES-MIP showed the highest binding capacity at pH 7. The kinetic and isotherm studies demonstrated good agreement with a pseudo-second-order kinetic model and Langmuir isotherm models, respectively. The thermodynamic study proved that the adsorption of BPA on DES-MIP was exothermic and spontaneous with ΔH 0 (-23.734 × kJ/mol) and ΔG 0 (-2.929 kJ/mol − ). 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Reusability experiments show that the DES-MIP can be recycled five times without significantly diminishing its adsorption capacity. As a result, it proved that the contribution of DES as a functional monomer alternative in MIP synthesis considerably improved the recognition of BPA adsorption.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><doi>10.1007/s10965-023-03581-1</doi><orcidid>https://orcid.org/0000-0002-4421-1745</orcidid></addata></record>
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subjects Adsorption
Analysis
Benzoyl peroxide
Bisphenol A
Bulk polymerization
Characterization and Evaluation of Materials
Chemistry
Chemistry and Materials Science
Choline
Ethylene glycol
Free radical polymerization
Free radicals
Imprinted polymers
Industrial Chemistry/Chemical Engineering
Isotherms
Methacrylic acid
Monomers
Optimization
Original Paper
Phenols
Polymer industry
Polymer Sciences
Polymerization
Polymers
Solvents
Synthesis
Thermal properties
Thermodynamics
title Evaluation of deep eutectic solvent as a new monomer for molecularly imprinted polymers for removal of bisphenol A
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