Waste of Mytella Falcata shells for removal of a triarylmethane biocide from water: Kinetic, equilibrium, regeneration and thermodynamic studies.

Waste of Mytella falcata shell was used as low-cost adsorbent to remove the biocide Basic Green 4 (BG4) from water. Shells were collected form trash nearby the lagoon were Mytella falcata is fished. After clean, dry and crushed, the powder was characterized by scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FT-IR), X-ray powder diffraction (XRD), and X-ray dispersive energy spectroscopy (EDS). Both kinetic and equilibrium adsorption tests are carried out. Adsorbent regenerability was tested during adsorption/desorption cycles, using a UV photo-regeneration process. The maximum adsorption capacity reached 539.24 mg.g-1 (60 °C), which was higher than those retrieved for other materials with similar origin. The kinetic results indicated that the process followed pseudo-second order model. Equilibrium data indicate an increase in BG4 adsorption capacity with temperature and Sips model had better fit for all the investigated temperatures (30, 40, 50 and 60 °C). The regeneration/reuse test indicated that the adsorbent is able to assure a BG4 removal above 70 % during five adsorption/desorption cycles evaluated. Thermodynamic parameters suggested that adsorption is spontaneous, endothermal, governed by chemisorption and with structural changes in the solid surface upon adsorption.

Mg-Fe layered double hydroxide with chloride intercalated: synthesis, characterization and application for efficient nitrate removal.

Mg-Fe layered double hydroxide intercalated with chloride (Mg-Fe-Cl LDH) was synthetized, characterized, and evaluated as adsorbent to remove nitrate from aqueous solution. The pH, initial nitrate concentration, adsorbent dosage, and particle size were investigated. Kinetic data was best represented by pseudo-second order model indicating that the rate limiting step was chemisorption. Intraparticle diffusion model indicates that adsorption kinetic is limited by external and intraparticle diffusion. Sips model was selected, based on R2, ARE, and AIC, to adequately represent the adsorption isotherms, which permits to affirm that the adsorption occurs in heterogeneous surface, obtaining the maximum adsorption capacity of 18.17 mg.g-1 at 30 oC. Thermodynamics parameters indicate that the adsorption was spontaneous, exothermic, and with structural modification. These findings come up with Mg-Fe-Cl LDH as a suitable adsorbent for nitrate and could contribute to its removal from the water and wastewater.

Wodyetia bifurcata biochar for methylene blue removal from aqueous matrix.

The endocarp of Wodyetia bifurcata was used to produce biochar by vacuum pyrolysis as an alternative adsorbent for methylene blue (MB) removal. The influence of different pyrolysis temperatures, particle diameters and activation agents in the adsorption process was studied. Kinetics and adsorption equilibrium were also evaluated. Biochar obtained at higher pyrolysis temperatures and activated with H3PO4 showed the best adsorptive capacities, achieving 83% of MB removal. The experimental data fitted better with pseudo-second order model. Isotherms performed at 25, 40, 50 and 60 °C showed that the adsorption of MB onto the activated biochar had no concentration dependence in the range studied. Experimental isotherms fitted well with the Freundlich and Sips models and the thermodynamic parameters suggested a physical adsorption mechanism in a heterogeneous surface, spontaneous at all temperatures evaluated. In brief, the activated carbon obtained from Wodyetia bifurcata can be a promising material for MB removal from aqueous solutions.

Evaluation of caffeine adsorption by MgAl-LDH/biochar composite.

In the present work, the composite MgAl-LDH/biochar using activated carbon from bovine bone as support for the layered double hydroxide particles was successfully synthesised and used as an alternative adsorbent for caffeine removal from water. Kinetic studies showed that the equilibrium was achieved in only 20 min of contact between the adsorbent and the adsorbate. The pseudo-first-order model represented the experimental data more satisfactorily (R2 = 0.95), suggesting a physical adsorption process. The isotherms were performed at three temperatures, in which it was observed the decrease in the adsorption in higher temperatures. It was obtained a maximum adsorption capacity of 26.219 mg/g at 40 °C, and the experimental data were better adjusted by Redlich-Peterson, R2 > 0.9942. In short, the study demonstrated that the composite was satisfactorily synthesised and its use in the caffeine removal was quite attractive, being a potential adsorbent for water treatment applications.

Determination of trace levels of triazines in corn matrices by bar adsorptive microextraction with a molecularly imprinted polymer.

This manuscript addresses the determination of triazines (ametryn, atrazine, simazine, and terbutryn) in corn matrices using bar adsorptive microextraction coated with a selective molecularly imprinted polymer phase following microliquid desorption and high-performance liquid chromatography with diode array detection. The molecularly imprinted polymer was synthesized using atrazine as a template and methacrylic acid as a functional monomer. Assays performed in 25 mL of ultrapure water samples spiked at 8.0 µg/L yielded 80-120 % recoveries under the evaluated experimental conditions. The method showed an accuracy (0.2 < bias < 17.9%), precision (relative standard deviation <17.4%), convenient detection (0.2 µg/L), and quantification (0.7 µg/L) limits, as well as linear dynamic ranges (0.8-24.0 µg/L) with remarkable determination coefficients (R(2) > 0.9926). The proposed analytical method was applied to monitor triazines in three types of corn matrices using the standard addition methodology. Experiments performed in corn samples spiked with triazines at the trace level (8.0 µg/kg of each analyte) gave rise to recoveries (81.0-119.4%) with good reproducibility and robustness. The proposed methodology is also easy to implement and showed to be a good analytical alternative to monitor triazines in complex matrices, when compared with other sorption-based microextraction techniques.