Search Results (3)

The treatment of chabazite (CHA), a natural zeolite, with the alkaline hydrothermal method to improve its ion-exchange capacity is a widely adopted route by environmental scientists for the purpose of better ammonium (${\mathrm{N}\mathrm{H}}_4^{+}$) removal from wastewater. This work addresses a noteworthy trend in environmental science, where researchers, impressed by the increased ion-exchange capacity achieved through alkaline hydrothermal treatment, often bypass the thorough material characterization of treated CHA. The prevalent misconception attributes the improved features solely to the parent zeolitic framework, neglecting the fact that corrosive treatments like this can induce significant alterations in the framework and those must be identified with correct nomenclature. In this work, alkaline-mediated hydrothermally treated CHA has been characterized through X-ray powder diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), solid-state magic-angle spinning nuclear magnetic resonance (MAS-NMR), high-resolution transmission electron microscopy (HRTEM), and energy-dispersive X-ray spectroscopy (EDS) and it is concluded that the treated samples have been transformed into a desilicated, aluminum (Al)-dense framework of analcime (ANA) with a low silica–alumina ratio and with a strikingly different crystal shape than that of parent CHA. This treated sample is further examined for its ${\mathrm{N}\mathrm{H}}_4^{+}$ removal capacity from synthetic wastewater in a fixed-bed column arrangement. It achieved a maximum ${\mathrm{N}\mathrm{H}}_4^{+}$ removal efficiency of 4.19 meq/g (75.6 mg/g of ${\mathrm{N}\mathrm{H}}_4^{+}$), twice that of the parent CHA. Moreover, the regeneration of the exhausted column yielded a regenerant solution, with 94% reclaimed ${\mathrm{N}\mathrm{H}}_4^{+}$ in it, which could be used independently as a nitrogenous fertilizer. In this work, the meticulous compositional study of zeolitic materials, a well-established practice in the field of material science, is advocated for adoption by environmental chemists. By embracing this approach, environmental scientists can enhance their comprehension of the intricate changes induced by corrosive treatments, thereby contributing to a more nuanced understanding of zeolitic behavior in environmental contexts. Full article

Five alkali-activated analcime (ANA) sorbents (ANA-MK 1, ANA 2, ANA 3, ANA-MK 4, and ANA-MK 5) were developed for ammonium (NH₄⁺) ion removal. Acid treatment and calcination were used as pre-treatments for analcime, and metakaolin (MK) was used as a blending agent in three sorbents. Sorption experiments were performed to evaluate the effects of sorbent dosage (1–20 g L⁻¹), initial NH₄⁺ ion concentration (5–1000 g L⁻¹), and contact time (1 min–24 h). ANA-MK 1, ANA 2, and ANA-MK 4 were the most efficient sorbents for NH₄⁺ ion removal, with a maximum experimental sorption uptake of 29.79, 26.00, and 22.24 mg g⁻¹, respectively. ANA 3 and ANA-MK 5 demonstrated lower sorption capacities at 7.18 and 12.65 mg g⁻¹, respectively. The results for the sorption of NH₄⁺ ions onto the alkali-activated analcime surfaces were modeled using several isotherms. The Langmuir, Freundlich, Sips, and Bi-Langmuir isotherms were the best isotherm models to represent the studied systems. The results of the kinetic studies showed the maximum NH₄⁺ ion removal percentage of the sorbents was ~80%, except for ANA-MK 5, which had a ~70% removal. Moreover, the pseudo-first-order, pseudo-second-order, and Elovich models were applied to the experimental data. The results showed that the sorption process for ANA-MK 1, ANA 2, ANA 3, and ANA-MK 4 followed the Elovich model, whereas the pseudo-second-order model provided the best correlation for ANA-MK 5. Full article

Co-processing of radioactive effluents with coal fly ash-derived materials is recognized as a resource-saving approach for efficient stabilization/solidification of radioactive components of wastewater. In this context, the paper is focused on the hydrothermal synthesis of Sr²⁺-bearing aluminosilicate/silicate phases as analogs of a mineral-like ⁹⁰Sr waste form using hollow glass-crystalline aluminosilicate microspheres from coal fly ash (cenospheres) as a glassy source of Si and Al (SiO₂-Al₂O₃)_glass) and Sr(NO₃)₂ solutions as ⁹⁰Sr simulant wastewater. The direct conversion of cenosphere glass in the Sr(NO₃)₂-NaOH-H₂O-(SiO₂-Al₂O₃)_glass system as well as Sr²⁺ sorption on cenosphere-derived analcime (ANA) in the Sr(NO₃)₂-H₂O-ANA system were studied at 150–200 °C and autogenous pressure. The solid and liquid reaction products were characterized by SEM-EDS, PXRD, AAS and STA. In the Sr(NO₃)₂-NaOH-H₂O-(SiO₂-Al₂O₃)_glass system, the hydrothermal processing at 150–200 °C removes 99.99% of the added Sr²⁺ from the solution by forming Sr-tobermorite and Sr-plagioclase phases. In the Sr(NO₃)₂-H₂O-ANA system, Sr²⁺ sorption on analcime results in the formation of solid solutions (Na_1−nSr_n/2)AlSi₂O₆·H₂O of the Na-analcime–Sr-wairakite series. The results can be considered as a basis for the development of environmentally sustainable technology for ⁹⁰Sr removal from wastewater and immobilization in a mineral-like form by co-processing waste from coal-fired and nuclear power plants. Full article