To evaluate the potential of Hg release and co-transport by colloids, it is important to understand how Hg, colloids and Hg-loaded colloids migrate in soils. Hg sorption by kaolinite and sand were nonlinear and fit the Langmuir model, with the maximum Hg sorption capacity being 1.2mg/g kaolinite and 0.11 mg/g sand. Co-transport of Hg and kaolinite was evaluated using: (1) 1 or 100 mg/L Hg or 100mg/L kaolinite, (2) 1 or 100 mg/L Hg mixed with 100mg/L kaolinite, (3) 1 or 100 mg/L Hg presorbed onto kaolinite, and (4) 25 0mg/L kaolinite in Hg-loaded sand columns. The presence of kaolinite (100 mg/L) reduced Hg's mobility through sand column by increasing deposition rate of Hg-loaded kaolinite. At 100 mg/L Hg, soluble Hg dominated Hg transport; but at 1 mg/L Hg, colloidal Hg (Hg sorbed on kaolinite) affected Hg transport. Preloading 100 mg/L Hg onto kaolinite (0.43 mg/g) reduced kaolinite's mobility with low recovery rate (78%), with Hg retardation (R=1) in Hg-loaded kaolinite being lower than Hg retardation at 100 mg/L Hg (R=1.287). The Hg recovery rate (93%) from Hg-loaded kaolinite at 1mg/L Hg was higher compared to 22% from 1 mg/L Hg. Kaolinite can serve as a carrier to enhance Hg transport in porous media, with 250 mg/L kaolinite mobilizing ~2.4% Hg presorbed onto sand media. Correlation analysis revealed that desorbed Hg was significantly correlated with kaolinite (r=0.81, P<0.0001). Hence kaolinite enhanced Hg transport in the sand media serving both as a carrier (Hg was loaded before transport) and as mobile colloids stripping Hg off the sand media (Hg was loaded during transport).
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http://dx.doi.org/10.1016/j.jhazmat.2012.01.061 | DOI Listing |
BMC Chem
January 2025
Nuclear Chemistry Department, Hot Laboratories Center, Egyptian Atomic Energy Authority, P.O. 13759, Cairo, Egypt.
In this work, selenium (IV) ions were adsorbed from aqueous solutions by the strongly basic anion exchange resin Amberlite IRA-400. The morphology of the resin before and after Se(IV) sorption was investigated using different techniques such as energy dispersive X-ray spectroscopy (EDX), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). To determine the ideal sorption conditions, a batch approach was used to examine the variables affecting Se(IV) sorption performance, including pH, shaking time, adsorbent dosage, initial metal ion concentration, and temperature.
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January 2025
Department of Biosystems and Technology, Swedish University of Agricultural Sciences, Alnarp 23456, Sweden. Electronic address:
Nickel (Ni) is required in trace amounts (less than 500 µg kg) in plants to regulate metabolic processes, the immune system, and to act as an enzymatic catalytic cofactor. Conversely, when nickel is present in high concentration, it is considered as a toxic substance. Excessive human nickel exposure occurs through ingestion, inhalation, and skin contact, ultimately leading to respiratory, cardiovascular, and chronic kidney diseases.
View Article and Find Full Text PDFInt J Biol Macromol
January 2025
School of Mechanical Engineering, Yeungnam University, Gyeongsan, Gyeongbuk 38541, Republic of Korea. Electronic address:
This study presents the preparation, characterization, and application of a novel Multi-walled carbon nanotubes/TiO/chitosan (MWCNT/TiO/CS) nanocomposite, prepared using a hydrothermal method, for the removal of malachite green (MG) dye from aqueous solutions. Adsorption studies revealed optimal dye removal within 15 min of adsorption equilibrium time, with maximum removal efficiency of 98.53 % at pH 7.
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January 2025
Department of Chemistry, Faculty of Science, Ege University, Bornova, Izmir 35040, Türkiye. Electronic address:
This study showcases the remarkable efficacy of quaternary ammonium-modified cellulose as a highly sustainable biosorbent for removing Sunset Yellow (SY) dye from water. Detailed analysis was conducted using infrared (FTIR) spectroscopy for structural changes and Scanning Electron Microscopy (SEM) for morphological changes. A minimal yet highly effective dose of 0.
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January 2025
Université Paris Cité, Institut de Physique du Globe de Paris, CNRS, F-75005 Paris, France. Electronic address:
Perfluorooctanesulfonic acid (PFOS) is one of the most investigated Per- and polyfluoroalkyl substances (PFAS) for being the strongest compound to eliminate and having adverse health concerns. In this work, we have conducted the sonochemical treatment of PFOS simulated water under high (500 kHz) and low (22 kHz) frequencies while monitoring the operational parameters via an integrated sonochemical system. The integrated advanced sonochemical system includes software to monitor treatment power, solution temperature and frequency while allowing distinctive control of the reaction conditions.
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