Four hundred tons of sulfamethazine are fed to livestock annually in North America to prevent disease and promote growth, but most of the drug is excreted unmetabolized into the environment. Because of slow degradation and high mobility, sulfamethazine contaminates groundwater supplies and causes aquatic ecosystem damage. Current water treatment methods to remove pharmaceuticals are not universally effective and have considerable limitations, which necessitate newer remediation techniques. Hypercrosslinked adsorbents, polystyrene polymers 100% crosslinked with methylene bridges, show promise because of high surface areas, high mechanical strength, and regenerable properties. This study screened four Purolite hypercrosslinked adsorbents (MN152, MN250, PAD400, and PAD600) to remove sulfamethazine from contaminated water and then characterized the most efficient resin, MN250, with batch adsorption and desorption experiments to optimize its use. Sulfamethazine adsorption onto MN250 displayed an L-class isotherm shape consistent with monolayer adsorption, negligible solute-solute interactions at the adsorbent surface, and decreasing activation energies of desorption with increasing surface coverage. MN250 had a maximum experimental adsorption capacity of 111 mg g, showing high correlation to the Langmuir and Freundlich models. Adsorption kinetics revealed prolonged adsorption over 59 h and were best described by Ho's pseudo-second-order model. There was minimal desorption from MN250 in distilled water, indicating an irreversible adsorption process. MN250's high capacity for sulfamethazine adsorption, minimal desorption in water, and ability to be regenerated make it a practical solution for sulfamethazine removal in areas that have contaminated groundwater supplies (e.g., areas near concentrated livestock operations), especially as current treatment methods have significant drawbacks.
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http://dx.doi.org/10.2134/jeq2012.0219 | DOI Listing |
Langmuir
January 2025
Department of Chemical Engineering, Canakkale Onsekiz Mart University,17100 Canakkale, Turkey.
Radioactive iodine, a key waste product of nuclear energy, has been a significant concern among nuclear materials because of its high volatility and its ability to easily enter the human metabolism. Porous materials containing a large number of N-heterocyclic units such as carbazole in the skeletons use as effective adsorbents showing high iodine capture capacities. Herein, a new carbazole-bismaleimide-based hyper-cross-linked porous organic polymer (CzBMI-POP) was successfully prepared from a new tetra-armed carbazole-maleimide monomer (Bis-Cz(BMI)), which contains biscarbazole units and maleimide side groups.
View Article and Find Full Text PDFAnal Chim Acta
February 2025
Food Laboratory of Zhongyuan, Luohe, 462000, Henan Province, PR China.
Background: Edible oils are susceptible to contamination with polycyclic aromatic hydrocarbons (PAHs) throughout production, storage, and transportation processes due to their lipophilic nature. The necessity of quantifying PAHs present in complex oil matrices at trace levels, which bind strongly to impurities in oil matrices, poses a major challenge to the accurate quantification of these contaminants. Therefore, the development of straightforward and effective methods for the separation and enrichment of PAHs in oil samples prior to instrumental analysis is paramount to guaranteeing food safety.
View Article and Find Full Text PDFEnviron Res
January 2025
Faculty of Chemistry, Adam Mickiewicz University, Poznań, Ul. Uniwersytetu Poznańskiego 8, 61-614, Poznań, Poland.
Development of new adsorbents for the efficient removal of organic pollutants from water is one of the most emerging environmental issues. Current studies in this field focus on improving the adsorption capacity of various materials and/or broadening the pH range in which the adsorbents can efficiently remove target pollutants. In this study, we designed bifunctional hyper-cross-linked polymers (HCPs) containing both carbonyl and amine species to investigate the effect of amine functional groups on the efficiency of adsorptive removal of non-steroidal anti-inflammatory drugs (NSAIDs) from water.
View Article and Find Full Text PDFPolymers (Basel)
December 2024
School of Chemistry and Chemical Engineering/State Key Laboratory Incubation Base for Green Processing of Chemical Engineering, Shihezi University, Shihezi 832003, China.
Int J Biol Macromol
December 2024
College of Chemistry and Materials, Huaihua University, Huaihua 418000, PR China; Hunan Engineering Laboratory for Preparation Technology of Polyvinyl Alcohol (PVA) Fiber Materia, Huaihua University, Huaihua 418000, PR China. Electronic address:
Lignin serves as an ideal substrate for the synthesis of chemically functionalized hyper-cross-linked resins due to the structural composition of its aromatic rings, aliphatic side chains, and multiple active functional groups. These resins have shown to be highly effective in the adsorption of aromatic compounds. In this study, hyper-cross-linked polymer (HCPs-3), synthesized using 1,3,5-triphenyl and lignin, demonstrated a significant adsorption capacity for aniline, with a maximum adsorption capacity (q) of 189.
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