Conversion of Glass Waste into Zeolite A Adsorbent for Efficient Ammonium Ion Adsorption from Aqueous Solution: Kinetic and Isotherm Studies
2025 (English)In: Processes, E-ISSN 2227-9717, Vol. 13, no 3, article id 678Article in journal (Refereed) Published
Abstract [en]
In this study, a zeolitic adsorbent (AGW-ZA) was successfully developed from glass waste (GW)-derived aluminosilicates. The GW, serving as the starting material, underwent alkaline activation and hydrothermal treatment to yield the AGW-ZA adsorbent, which exhibited a surface area of 216.48 m2/g. The AGW-ZA demonstrated significantly higher ammonium (NH4+) ion adsorption (142.5 mg/g at 1000 mg/L) than pristine GW (80.0 mg/g). Optimal adsorption experimental parameters were identified (0.1 g dosage, pH = 7, and 10 h contact time) to determine the maximum NH4+ ions’ adsorption potential by adsorbents. Kinetic and isotherm models were applied to experimental data to describe the adsorption mechanisms. The pseudo-second-order model provided the best fit for both AGW-ZA and pristine GW, indicating that the adsorption process is followed by chemical interaction via ion exchange. Regarding isotherms, the Freundlich model was most suitable for AGW-ZA, signifying that NH4+ ions adsorbed on heterogeneous adsorbent surfaces by forming multilayers, while the Temkin model fit the pristine GW data, indicating the chemisorption nature with medium adsorbate–adsorbent interactions above the heterogeneous surface. This study explores the potential of transforming discarded GW into a high-performance zeolitic adsorbent for the mitigation of environmental pollution by removing NH4+ ions from wastewater while simultaneously addressing waste management challenges.
Place, publisher, year, edition, pages
Multidisciplinary Digital Publishing Institute (MDPI) , 2025. Vol. 13, no 3, article id 678
Keywords [en]
glass waste, zeolite A, adsorption, ammonium ion, kinetics, adsorption isotherms
National Category
Analytical Chemistry Environmental Sciences
Research subject
Engineering Materials
Identifiers
URN: urn:nbn:se:ltu:diva-112272DOI: 10.3390/pr13030678Scopus ID: 2-s2.0-105001095887OAI: oai:DiVA.org:ltu-112272DiVA, id: diva2:1950278
Funder
Sida - Swedish International Development Cooperation Agency, 13486Luleå University of Technology, 228121
Note
Validerad;2025;Nivå 2;2025-04-07 (u8);
Funder: National Natural Science Foundation of China (52020105011)
Full text license: CC BY
2025-04-072025-04-072025-04-08Bibliographically approved