Removal of arsenic from water reservoirs is the issue of great concern in many places around the globe. As adsorption is one of the most efficient techniques for treatment of As-containing media, thus the present study concerns application of iron oxides-hydroxides (akaganeite) as adsorbents for removal of this harmful metal from aqueous solution. Two types of akaganeite were tested: synthetic one (A) and the same modified using hexadecyltrimethylammonium bromide (AM). Removal of As was tested in batch studies in function of pH, adsorbent dosage, contact time, and initial arsenic concentration. The adsorption isotherms obey Langmuir mathematical model. Adsorption kinetics complies with pseudo-second-order kinetic model, and the constant rates were defined as 2.07 × 10−3and 0.92 × 10−3 g mg−1 min−1 for the samples (A) and (AM), respectively. The difference was caused by significant decrease in adsorption rate in initial state of the process carried out for the sample AM. The maximum adsorption capacity achieved for (A) and (AM) akaganeite taken from Langmuir isotherm was 148.7 and 170.9 mg g−1, respectively. The results suggest that iron oxides-hydroxides can be used for As removal from aqueous solutions.
The aim of this work is to investigate the application of fly ash adsorbent for removal of arsenite ions from dilute solution (100-1,000 ppm). Experiments were carried out using material from the "Turów" (Poland) brown-coal-burning power plant, which was wetted, then mixed and tumbled in a granulator to form spherical agglomerates. Measurements of arsenic adsorption from aqueous solution were carried out at room temperature and natural pH of fly ash agglomerates, in either a shaken flask or circulating column, to compare two different methods of contacting solution with adsorbent. Adsorption isotherms of arsenic were determined for agglomerated material using the Freundlich equation. Kinetic studies indicated that sorption follows a pseudo-second-order model. Preferable method to carry out the process is continuous circulation of arsenite solution through a column.
Present contribution describes modified Stöber synthesis of silica nanoparticles in oil-in-water microemulsion, formulated using heptane, 2-ethylhexanol, Tween® 85 nonionic surfactant, and tetraethyl orthosilicate (TEOS). After some specified incubation time, ammonium hydroxide was added and the reaction mixture was stirred for 24 hours at room temperature. Prior to synthesis, pseudoternary diagram was created for oil-rich area and Winsor IV region was identified. These microemulsions were used for synthesis of silica particles. Resulting particles were characterized by dynamic light scattering, electrokinetic measurements, specific surface area measurements, and powder diffraction. Particles’ diameter was ranging between ca. 130 and 500 nm; usually monodisperse distribution was obtained. The specific surface area of nanoparticles was ranging between 250 and 300 m2/g. Notably, productivity per unit volume of solution was 3 to 5 times higher than for previously reported procedures. Our method can be extended, because polymeric materials can be added to dispersed aqueous phase. In our studies, β-cyclodextrin and hydroxyethylcellulose have been used, giving particles between 170 and 422 nm, with the surface area larger than 300 m2/g.
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