A batch adsorption process was applied to investigate the removal of perchlorate (ClO4 (-)) from water by graphene. In doing so, the thermodynamic adsorption isotherm and kinetic studies were also carried out. Graphene was prepared by a facile liquid-phase exfoliation. Graphene was characterized by Raman spectroscopy, Fourier-transform infrared spectroscopy, powder X-ray diffraction, scanning electron microscope, and zeta potential measurements. A systematic study of the adsorption process was performed by varying pH, ionic strength, and temperature. The adsorption efficiency of graphene was 99.2 %, suggesting that graphene is an excellent adsorbent for ClO4 (-) removal from water. The rate constants for all these kinetic models were calculated, and the results indicate that second-order kinetics model was well suitable to model the kinetic adsorption of ClO4 (-). Equilibrium data were well described by the typical Langmuir adsorption isotherm. The experimental results showed that graphene is an excellent perchlorate adsorbent with an adsorbent capacity of up to 0.024 mg/g at initial perchlorate concentration of 2 mg/L and temperature of 298 K. Thermodynamic studies revealed that the adsorption reaction was a spontaneous and endothermic process. Graphene removed the perchlorate present in the water and reduced it to a permissible level making it drinkable.
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http://dx.doi.org/10.1007/s11356-013-1499-y | DOI Listing |
Rapid Commun Mass Spectrom
February 2025
School of Earth, Environment & Society, McMaster University, Hamilton, ON, Canada.
Rationale: The stable isotope compositions of atmospheric CO can provide useful insight into various geochemical processes and carbon cycles on Earth, which is critical for understanding of Earth's changing climate. Here, we present a simple and cost-effective analytical method for the collection and measurement of carbon and oxygen isotope compositions of atmospheric CO.
Methods: Air samples of ~150 mL were collected individually or collectively using our simple active air collection system and then extracted on a vacuum purification line to remove noncondensable gases and atmospheric water vapor.
J Hazard Mater
February 2025
University of Delaware, Newark, DE 19716, USA.
Munition constituents (MC) in stormwater runoff have the potential to move these pollutants into receiving bodies at military installations. Here we present further evaluation of a passive and sustainable biofilter technology for removal of dissolved MC from simulated surface runoff by combined sorption-biodegradation processes under dynamic flow conditions. Columns were packed with MC sorbents Sphagnum peat moss and cationized (CAT) pine shavings with and without wood-based biochar.
View Article and Find Full Text PDFChemistryOpen
November 2024
Departamento de Química Inorgánica, Universidad de Santiago de Compostela, E-, 15782, Santiago de Compostela, Spain.
J Hazard Mater
November 2024
Water Science and Technology group (WaSTe), Department of Civil Engineering, University of Salerno, Via Giovanni Paolo II 132, Fisciano, SA 84084, Italy. Electronic address:
Real lindane landfill leachate (HCH-LL) is characterised by high chlorinated organic compounds concentrations (primarily hexachlorocyclohexane (HCH) isomers and degradation products generated during more than 40 years of ageing), posing environmental and human health risks. In this work, the co-treatment of real HCH-LL (pre-treated via electro-oxidation (EO)) and urban wastewater using an activated sludge process operated in an anoxic/oxic sequencing batch (A/O-SBR) mode was investigated. EO tests were conducted employing either a boron-doped diamond (BDD) anode or a dimensionally stable anode (DSA), resulting in effective HCH isomers removal (>93 % after 20 Ah/L).
View Article and Find Full Text PDFChemosphere
September 2024
Department of Civil Engineering, Zhejiang University, 866 Yuhangtang Rd., Hangzhou, 310058, China; Key Laboratory of Drinking Water Safety and Distribution Technology of Zhejiang Province, Zhejiang University, 866 Yuhangtang Rd., Hangzhou, 310058, China. Electronic address:
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