Insights on adsorption of carbamazepine onto iron oxide modified diatomaceous earth: Kinetics, isotherms, thermodynamics, and mechanisms.

To ameliorate adsorbent recovery by an external magnetic field, naturally occurring diatomaceous earth (DE) was modified with iron-oxide, characterized and applied for adsorption of carbamazepine (CBZ) from synthetic wastewater using batch equilibration method. The fabricated adsorbent was characterized using XRF, XRD, SEM-EDX, FT-IR, BET surface area analysis, VSM and pH of point of zero charge (pHpzc) determination. The adsorption rate was described by the pseudo-first-order (PFO) model suggesting a physisorption controlled rate-determining step. Equilibrium adsorption data were fitted to linear and nonlinear isotherm models, viz Langmuir and Freundlich models, and were best described by Freundlich nonlinear equations implying heterogeneous multilayer adsorption. The best-fitting kinetic and isotherm model was determined using four mathematical error functions. The thermodynamic parameters, namely enthalpy (ΔH = -26.4 kJ mol-1), Gibbs free energy (ΔG = -2.22 kJ mol-1 at 298 K), entropy (ΔS = -34.0 kJ mol-1), indicated that the adsorption was a spontaneous, exothermic, and physical process. The adsorption mechanism is postulated to involve cation-π interactions. Modified diatomaceous earth is a potentially excellent, low-cost, and novel sorbent for CBZ adsorption with 88% removal in 180 min and provides a possible alternative adsorbent for wastewater treatment.

Comparative studies in electrochemical degradation of sulfamethoxazole and diclofenac in water by using various electrodes and phosphate and sulfate supporting electrolytes.

In this study, the electro-oxidation capacities of Na2SO4 and potassium phosphate buffer supporting electrolytes were tested and compared for destruction of the sulfamethoxazole (SMX) and diclofenac (DCF) on platinum (Pt) electrode and graphite carbon electrode in aqueous medium. The suitability of pharmaceutical active compounds (PhACs) for electrochemical oxidation was tested by cyclic voltammetry (CV) technique performed in the potential range -1.5 to +1.5 V versus Ag/AgCl, which confirmed the electro-activity of the selected PhACs. The degradation and mineralization were monitored by ultraviolet (UV)-Vis spectrophotometry and HPLC. 0.1 M Na2SO4 supporting electrolyte was found to be more effective for mineralization of SMX and DCF, with efficiency of 15-30% more than the 0.1 M phosphate buffer supporting electrolyte on the platinum (Pt) and carbon electrodes. The Pt electrode showed better performance in the degradation of the two PhACs while under the same conditions than the carbon electrode for both 0.1 M Na2SO4 and 0.1 M potassium phosphate buffer supporting electrolytes. The SMX and DCF degradation kinetics best fitted the second-order reaction, with rate constants ranging between 0.000389 and 0.006 mol(2) L(-2) min(-1) and correlation coefficient (R(2)) above 0.987. The second-order degradation kinetics indicated that the rate-determining step in the degradation could be a chemical process, thus suggesting the active involvement of electrolyte radical species in the degradation of SMX and DCF. Results obtained from a real field sample showed a more than 98% removal of the PhACs from the wastewater by electrochemical degradation.

The dissipation of carbofuran in two soils with different pesticide application histories within Nzoia River Drainage Basin, Kenya.

The dissipation of carbofuran from soils within the Nzoia River Drainage Basin in Kenya was studied under real field conditions for 112 days. Results showed significantly enhanced dissipation of carbofuran with half life (DT50) values of 8 days (p = 0.038) in soils with prior exposure to carbofuran compared to 19 days in soils with no application history. At the end of the experiment, residues of 2.57% and 9.36% of the initial carbofuran applied were recorded in the two types of soil, respectively. Carbofuran metabolites identified in the study were 3-keto carbofuran and carbofuran phenol with 5.84% and 15.0% remaining in soils with prior exposure, respectively. Soils with no application history recorded 16.05% and 12.82% of 3-keto carbofuran and carbofuran phenol metabolites, respectively.

The influence of filter mud compost and Tithonia diversifolia leaves on the dissipation of diuron in soils within the Nzoia River Drainage Basin, Kenya.

The aim of the study was to evaluate the environmental impact of filter mud compost and Tithonia diversifoila amendments on the dissipation of diuron in sugarcane cultivated soils. Filter mud compost is the by-product of sugarcane processing, while T. diversifoila is a common local plant that grows within the study region. The dissipation of diuron was significantly enhanced with DT(50) of 15 and 16 days (p < 0.05) in soils amended with filter mud compost and T. diversifoila, respectively compared to 26 days in non-amended soils. Residues of 0.93 %, 1.83 % and 5.40 % of the initial applied diuron were recorded at the end of the experiment in the three treatments, respectively. The residues of 3,4-dichlorophenylmethylurea metabolite were 22.93 %, 25.92 % and 30.93 %, while 10.19 %, 12.19 % and 15.46 % of 3,4-dichloroaniline metabolite remained in soil after 112 days in the three treatments, respectively.