ABSTRACT
High concentrations of graphene oxide (GO), a nanoparticle substance with rapid manufacturing development, have the ability to penetrate the soil surface down to the mineral-rich subsurface layers. The destiny and distribution of such an unusual sort of nanomaterial in the environment must therefore be fully understood. However, the way the chemistry of solutions impacts GO nanoparticle adsorption on clay minerals is still unclear. Here, the adsorption of GO on clay minerals (e.g., bentonite and kaolinite) was tested under various chemical conditions (e.g., GO concentration, soil pH, and cation valence). Non-linear Langmuir and Freundlich models have been applied to describe the adsorption isotherm by comparing the amount of adsorbed GO nanoparticle to the concentration at the equilibrium of the solution. Our results showed fondness for GO in bentonite and kaolinite under similar conditions, but the GO nanoparticle adsorption with bentonite was superior to kaolinite, mainly due to its higher surface area and surface charge. We also found that increasing the ionic strength and decreasing the pH increased the adsorption of GO nanoparticles to bentonite and kaolinite, mainly due to the interaction between these clay minerals and GO nanoparticles' surface oxygen functional groups. Experimental data fit well to the non-linear pseudo-second-order kinetic model of Freundlich. The model of the Freundlich isotherm was more fitting at a lower pH and higher ionic strength in the bentonite soil while the lowest R2 value of the Freundlich model was recorded at a higher pH and lower ionic strength in the kaolinite soil. These results improve our understanding of GO behavior in soils by revealing environmental factors influencing GO nanoparticle movement and transmission towards groundwater.
ABSTRACT
LaFeO3 perovskite is prepared by the cellulose-modified microwave-assisted citrate method using two different biomasses as a cellulose source; rice straw (RS) and banana peel (BP). The prepared samples are assigned as LaFeO3/cellulose-RS and as LaFeO3/cellulose-BP, respectively. Raman Spectra prove the presence of perovskite and cellulose phases, as well as biochar resulted from the thermal treatment of the cellulose. LaFeO3/cellulose-RS has a cauliflower morphology while, two phases are observed for LaFeO3/cellulose-BP, mesoporous cellulose phase and octahedral LaFeO3 nanoparticles as shown by scanning electron microscope (SEM) images. LaFeO3/cellulose-BP has higher porosity and larger BET surface area than LaFeO3/cellulose-RS. Both samples are applied for the removal of Pb(II) ions from aqueous solution by adsorption. The adsorption follows Langmuir isotherm, with maximum adsorption capacities of 524 and 730 mg/g for LaFeO3/cellulose-RS and LaFeO3/cellulose-BP, respectively. Cellulose precursors from different biomasses affect structural and morphological properties of LaFeO3/cellulose samples as well as the sorption performance for Pb(II) ions. BP is more recommended than RS, as a biomass, in the present study.
ABSTRACT
LaFeO3/biochar composite is prepared by cellulose-modified microwave-assisted method at 450 °C. The structure is identified by Raman spectrum which, consists of characteristics biochar bands and octahedral perovskite chemical shifts. The morphology is examined by scanning electron microscope (SEM); two phases are observed, rough microporous biochar and orthorhombic perovskite particles. The BET surface area of the composite is 57.63 m2/g. The prepared composite is applied as a sorbent for the removal of Pb2+, Cd2+, and Cu2+ ions from aqueous solutions and wastewater. The adsorption ability reaches a maximum at pH > 6 for Cd2+, and Cu2+ ions, and is pH-independent for Pb2+ ions adsorption. The adsorption follows pseudo 2nd order kinetic model, Langmuir isotherm for Pb2+ ions, and Temkin isotherms for Cd2+, and Cu2+ ions. The maximum adsorption capacities, qm, are 606, 391, and 112 mg/g for Pb2+, Cd2+, and Cu2+ ions, respectively. The electrostatic interaction is responsible for the adsorption of Cd2+, and Cu2+ ions on LaFeO3/biochar composite. In case of Pb2+ ions form a complex with the surface functional groups of the adsorbate. LaFeO3/biochar composite shows high selectivity for the studied metal ions and excellent performance in real samples. The proposed sorbent can be easily regenerated and effectively reused.