Synthesis of molecularly imprinted polymer for the removal of cyanazine from aqueous samples

Abstract

BackgroundCyanazine (CYZ) is one of the triazine herbicides to prevent broadleaf grass and weeds in crops. Despite its affordability and productivity in increasing crop yield, the extensive usage of CYZ contributes to environmental pollution and poses risks to living organisms. Most research has focused on detecting CYZ in the environment and its toxicity to humans and the ecosystem. For these reasons, molecular imprinting technology (MIT) can be applied to produce an effective adsorbent material of high binding affinity and selectivity towards its target compound which is known as molecularly imprinted polymers (MIPs). In this study, MIP was prepared by precipitation polymerization using CYZ as a template molecule, methacrylic acid (MAA), acrylamide (AAm) and 4-vinylpyridine (4VP) as functional monomers, and ethylene glycol dimethacrylate (EGDMA) as cross-linker in the ratio of 1:6:12, respectively. The effects of contact time, initial concentration, pH, and polymer dosages on the adsorption efficiencies of MIPs were also investigated in this study.ResultsMIPs of CYZ were successfully synthesized by precipitation polymerization method with a non-covalent approach using different functional monomers such as methacrylic acid (MAA), acrylamide (AAm) and 4-vinylpyridine (4VP). For the comparison study, the non-imprinted polymer (NIP) was synthesized without the addition of CYZ, the template molecule. The FTIR analysis indicated the interactions among CYZ and functional monomers (MAA, AAm or 4VP) in the presence of EGDMA as a cross-linker. The FESEM analysis showed that only MIP (AAm) and NIP (AAm) had regular and spherical polymer particles while MIP (MAA), NIP (MAA), MIP (4VP) and NIP (4VP) were agglomerated and irregular in shape. The EDX analysis showed that the MIPs were mainly composed of carbon and oxygen. Meanwhile, the BET analysis of MIP (AAm) had higher surface area, total pore volume and average pore radius than that NIP (AAm). Based on the batch binding study, MIP (AAm) (83.30%) had the highest binding efficiency than the MIP (MAA) (76.96%) and MIP (2VP) (76.90%) at a contact time of 240 min. The optimum conditions for the highest binding efficiency of MIP (AAm) were obtained at an initial concentration of 6 ppm, pH 7 and polymer dosage of 0.1 g polymer beads. The adsorption efficiency of MIP (AAm) with CYZ at the optimum parameters resulted in 86.39%. The selectivity test showed that MIP (AAm) was more selective towards CYZ than AME, the competitive compound with relative selectivity coefficient of 2.36. The kinetic isotherm of MIP (AAm) was best explained according to the pseudo-second-order kinetic model while the adsorption isotherm of MIP (AAm) was based on the Langmuir adsorption isotherm model. The MIP (AAm) was tested in the distilled water (DIW), tap water and river water spiked with CYZ and a substantial amount of CYZ was removed with a recovery of 86.67%, 84.75% and 84.69%, respectively.ConclusionThe MIPs of CYZ were successfully synthesized by the precipitation polymerization method using different functional monomers. Among those MIPs, MIP (AAm) showed the highest rebinding efficiency and therefore this MIP was selected for further studies. The best combination of CYZ, AAm was the main factor that contributed to the morphological and chemical properties, as well as the efficiency and selective binding performance of MIP (AAm). Since MIP (AAm) showed a substantial removal efficiency of CYZ in the environment specifically water sources, it has the capability to act as an adsorbent material for various purposes such as solid-phase extraction techniques and a stationary phase in various chromatographic techniques.Graphical