Removal of bisphenol A from aqueous media using a highly selective adsorbent of hybridization cyclodextrin with magnetic molecularly imprinted polymer
water samples
Molecular imprinting
Science
Health, Toxicology and Mutagenesis
Organic chemistry
Azobisisobutyronitrile
molecularly imprinted polymer
01 natural sciences
Catalysis
Analytical Chemistry
Polymerization
Bisphenol A
Chemical engineering
Engineering
Molecularly Imprinted Polymers
FOS: Chemical sciences
Radical polymerization
Aqueous solution
Cyclodextrin
Selectivity
Polymer
Chiral Separation in Chromatography
Spectroscopy
FOS: Chemical engineering
Analytical Chemistry Techniques
0105 earth and related environmental sciences
TP1080-1185 Polymers and polymer manufacture
Molecularly imprinted polymer
Metal Ion-Imprinted Polymers
Benzoyl peroxide
bisphenol a
Freundlich equation
Q
Fourier transform infrared spectroscopy
Endocrine Disruption by Chemical Exposure
Methacrylic acid
620
543
Nuclear chemistry
Monomer
Chemistry
β-cyclodextrin
adsorption
Physical Sciences
Environmental Science
Adsorption
Bulk polymerization
DOI:
10.1098/rsos.201604
Publication Date:
2021-03-10T08:06:56Z
AUTHORS (6)
ABSTRACT
In this study, a unique magnetic molecularly imprinted polymer (MMIP) adsorbent towards bisphenol A (BPA) as a template molecule was developed by bulk polymerization using β-cyclodextrin (β-CD) as a co-monomer with methacrylic acid (MAA) to form MMIP MAA–βCD as a new adsorbent. β-CD was hybridized with MAA to obtain water-compactible imprinting sites for the effective removal of BPA from aqueous samples. Benzoyl peroxide and trimethylolpropane trimethacrylate were used as the initiator and cross-linker, respectively. The adsorbents were characterized by Fourier transform infrared spectroscopy, scanning electronic microscopy, transmission electron microscopy, vibrating sample magnetometer, Brunauer–Emmett–Teller and X-ray diffraction.1H nuclear magnetic resonance spectroscopy was used to characterize the MAA–βCD and BPA–MAA–βCD complex. Several parameters influencing the adsorption efficiency of BPA such as adsorbent dosage, pH of sample solution, contact time, initial concentrations and temperature as well as selectivity and reusability study have been evaluated. MMIP MAA–βCD showed significantly higher removal efficiency and selective binding capacity towards BPA compared to MMIP MAA owing to its unique morphology with the presence of β-CD. The kinetics data can be well described by the pseudo second-order kinetic and Freundlich isotherm and Halsey models best fitted the isotherm data. The thermodynamic studies indicated that the adsorption reaction was a spontaneous and exothermic process. Therefore, MMIP based on the hybrid monomer of MAA–βCD shows good potential of a new monomer in molecularly imprinted polymer preparation and can be used as an effective adsorbent for the removal of BPA from aqueous solutions.
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