Synthesis of N-isopropyl acrylamide copolymerized acrylic acid caped with Dibenzo-18-crown-6 composite for selective separation of Co-60 radioisotope from radioactive liquid waste containing Cs-137

A new selective polymeric composite capped with crown ether was successfully synthesized using N-isopropyl acrylamide copolymerized acrylic acid paired with Dibenzo-18-crown-6, P(NIPAm-Co-AA-DB 18C-6), by Gamma irradiation and ultrasonic homogenizer polymerization. Scanner electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), and dynamic light scattering were used to characterize the selected polymeric composite's chemical and physical constitution. SEM shows a rough irregular surface, and FTIR spectra confirmed the function groups of P(NIPAm-Co-AA-DB 18C-6). Moreover, a systematic study of monomer and crown ether concentration was investigated to enhance the composite's performance. The behavior of the synthetic composite toward the selective separation of Co-60 from Cs-137 in a binary system was evaluated. Effects of pH, contact time, and initial ion concentration were investigated in a batch mode and the maximum capacity reached 108.0 mg/g for Co-60 and 82.0 mg/g for Cs-137. Four Kinetic models were investigated (pseudo-first-order, pseudo-second-order, Elovich, and Intra-particle diffusion). Regarding the calculated parameters, pseudo-second-order and Elovich models are the most describing the sorption process, indicating the chemisorptions process. Six adsorption isotherms were examined, two-parameter models (Langmuir, and Freundlich) and three-parameter models (Redlich-Peterson, Khan, Sips, and Hills). The best-fitted isotherm was identified using three error methodological approaches: the correlation coefficient (R-2), the chi-square test (chi(2)), and the root-mean-square error. Isotherm models fit the experimental values in the following sequence: Khan > Rdlish-Peterson > Hills > Sips. Finally, an application for column separation was conducted, and Co-60 was completely separated from Cs-137 by 0.1 M HNO3. These findings indicate promising applications in the successive separation of Co-60 from radioactive liquid waste containing Cs-137 from Egyptian reactors.