Microstructure of gamma-ray developed polymeric nanocomposite respecting cesium and cobalt removal from aqueous solutions

Abstract

The nanoparticles of fly ash (FA) were obtained by high energy ball milling of their parent Class C kind for subsequent synthesis of poly(acrylamide-acrylic acid)/fly ash (poly(AM-AA)/FA) nanocomposite. The gamma-radiation induced polymerization was applied to achieve this concern. Different techniques were utilized to characterize such nanocomposite. The sorption abilities of the synthesized nanocomposite toward 60Co2+ and 134Cs + radionuclides were evaluated using batch and fixed-bed column approaches. Batches were designed at constants of solution pH (6.5–7.0 ± 0.02), nanocomposite particle size and dosage (106–250 μm and 0.1 L/g, respectively). The microstructure of such nanocomposite (<100 nm) was mainly amorphous with porous rough surfaces containing homogenous distribution of the incorporated nano-FA. About 56.46 and 47.9 mg/g of Co2+ and Cs+ were sorbed at equilibrium with an ion exchange reaction mechanism. Langmuir, Freundlich and Dubinin–Radushkevich D–R isotherm model parameters were calculated indicating the favorability of all sorption processes. The spontaneous and endothermic natures of sorption were observed by the calculated ΔG° and ΔH° thermodynamic parameters, respectively. Thomas, Yoon–Nelson and Adams Bohart models were fitted to the fixed-bed column data at varied conditions. The predicted sorption capacities of Thomas were very close to those obtained experimentally. Modeling of the fixed-bed column data dominates that the external mass transfer kinetics was predominant in the initial parts of the fixed-beds. Values required for retaining 50% of the initial sorbate concentration were extended from 89.05 to 68.55 to 177.2 and 149.3 min for 60Co2+ and 134Cs + radionuclides, respectively, by increasing bed depth from 1.5 to 3.0 cm. Modification of FA to its nano-scale form with the subsequent synthesis of a nanocomposite material having sorption capabilities made a duplicate beneficial environmental concern.