TY - JOUR
T1 - Molecularly imprinted polymer for the removal of diclofenac from water: Synthesis and characterization
AU - Sánchez-Martín, María-Jesús
AU - Sebastián Pérez, Rosa Maria
AU - Valiente Malmagro, Manuel
AU - López-Mesas, Montserrat
AU - Samah, Nurlin Abu
PY - 2018/8/1
Y1 - 2018/8/1
N2 - Contaminants of Emerging Concerns (CECs) have been introduced as one type of recalcitrant pollutant sources in water. In this study, the non-steroidal anti-inflammatory drug diclofenac (DCF) has been removed from water solutions using Molecularly Imprinted Polymer (MIP), synthetized via bulk polymerization with allylthiourea (AT) as the functional monomer and using DCF as template (MIP-DCF). DCF detection has been performed by UV spectrophotometer. From the kinetic study in batch mode, approximately 100% of removal is observed by using 10 mg of MIP-DCF, with an initial concentration of 5 mg/L of DCF at pH 7, within 3 min and agitated at 25 °C. In continuous flow mode study, using a cartridge pre-packed with 10 mg of MIP-DCF, a high adsorption capacity of 160 mg DCF/g MIP was obtained. To study the porosity of MIPs, scanning electron microscopy (SEM) has been used. In order to characterize the chemical interaction between monomer and template, the pre-polymerization mixture for MIP and DCF has also been studied by H NMR. One of the chemical shift observed has been related to the formation of a complex between amine protons of thiourea group of AT with carboxylic acid on DCF. In conclusion, the developed MIP works as a good adsorbent for DCF removal, and is selective to DCF in the presence of indomethacin and ibuprofen.
AB - Contaminants of Emerging Concerns (CECs) have been introduced as one type of recalcitrant pollutant sources in water. In this study, the non-steroidal anti-inflammatory drug diclofenac (DCF) has been removed from water solutions using Molecularly Imprinted Polymer (MIP), synthetized via bulk polymerization with allylthiourea (AT) as the functional monomer and using DCF as template (MIP-DCF). DCF detection has been performed by UV spectrophotometer. From the kinetic study in batch mode, approximately 100% of removal is observed by using 10 mg of MIP-DCF, with an initial concentration of 5 mg/L of DCF at pH 7, within 3 min and agitated at 25 °C. In continuous flow mode study, using a cartridge pre-packed with 10 mg of MIP-DCF, a high adsorption capacity of 160 mg DCF/g MIP was obtained. To study the porosity of MIPs, scanning electron microscopy (SEM) has been used. In order to characterize the chemical interaction between monomer and template, the pre-polymerization mixture for MIP and DCF has also been studied by H NMR. One of the chemical shift observed has been related to the formation of a complex between amine protons of thiourea group of AT with carboxylic acid on DCF. In conclusion, the developed MIP works as a good adsorbent for DCF removal, and is selective to DCF in the presence of indomethacin and ibuprofen.
KW - Contaminant of emerging concerns
KW - Diclofenac
KW - Molecularly imprinted polymer
U2 - 10.1016/j.scitotenv.2018.03.087
DO - 10.1016/j.scitotenv.2018.03.087
M3 - Article
SN - 0048-9697
VL - 631-632
SP - 1534
EP - 1543
JO - Science of the total environment
JF - Science of the total environment
ER -