The effectiveness and adsorption mechanism of iron-carbon nanotube composites for removing phosphate from aqueous environments.

This study successfully employed iron-carbon nanotubes (Fe-CNT) to recover phosphate (P) from water. We examined the effects of various iron concentrations denoted by Fe-CNT-1 and Fe-CNT-2 on P removal and compared them with pristine carbon nanotubes (CNTs). The adsorption capacity of Fe-CNTs was much better than pristine CNTs.

Biogeochemical Alteration of an Aquifer Soil during In Situ Chemical Oxidation by Hydrogen Peroxide and Peroxymonosulfate.

In this study, the effects of in situ chemical oxidation (ISCO) on the biogeochemical properties of an aquifer soil were evaluated. Microcosms packed with an aquifer soil were investigated for 4 months in two phases including oxidant exposure (phase I) and biostimulation involving acetate addition (phase II). The geochemical and microbial alterations from different concentrations (0.

Individual and simultaneous degradation of sulfamethoxazole and trimethoprim by ozone, ozone/hydrogen peroxide and ozone/persulfate processes: A comparative study.

This study investigates the individual and simultaneous degradation and mineralization of the antibiotics, sulfamethoxazole (SMX) and trimethoprim (TMP) in aqueous solution by ozonation, ozone-activated persulfate (PS) and hydrogen peroxide (HO) processes. The trials were carried out in a semi-continuous column bubble reactor with an ozone diffuser located at the bottom of the column for a period of 2 h. Furthermore, the efficiency of studied processes were evaluated at two different initial pH and various doses of oxidants.

Defective, oxygen-functionalized multi-walled carbon nanotubes as an efficient peroxymonosulfate activator for degradation of organic pollutants.

Herein, the defects and surface oxygen functionalities of multi-walled carbon nanotubes (MWCNTs) derived from a solid state reaction are demonstrated to be effective in the activation of peroxymonosulfate (PMS) for organic pollutant degradation. The catalytic activity of defective, oxygen-functionalized CNTs (dCNTs) is much better than bare CNTs, which stems from many active sites on the CNT surface, including structural defects and carbonyl functional groups, and excellent electrical conductivity. Furthermore, the effect of several operational factors and water conditions on the degradation rate of the targeted pollutant and material stability are comprehensively evaluated for the practical application of the dCNT/PMS-coupled process.