Electrochemically-driven regeneration of iron (II) enhances Fenton abatement of pesticide cartap.

Cartap is a carbamate insecticide intended to protect crops such as rice, tea, and sugarcane. Cartap in the environment presents a serious threat to non-target organisms through direct exposure or via biomagnification. Electro-assisted Fenton technology taps the potential of Fenton reagents to degrade cartap. Electrochemical reduction of iron accelerates catalyst regeneration. Cartap degradation was first investigated by varying reaction pH, as well as the initial H2O2 and Fe2+ dosage, followed by optimization studies using central composite design. Parametric results indicate the highest cartap removal of 98.10% was achieved at 1.6 pH, 3.0 mM Fe2+, and 40 mM H2O2 at I = 1.0 A and t = 30 min. These results notoriously surpass conventional Fenton that only achieved 53.8% cartap removal under similar conditions. The hybridization of Fenton process through electrochemical regeneration enhances removal and increases degradation kinetic up to a pseudo-first-order rate constant value of 21.30 × 10-4 s-1. Effects of coexisting inorganic salts PO43-, NO3-, and Cl- at 1 mM and 10 mM concentrations were investigated. These results demonstrate that Fenton electrification as process intensification alternative can enhance the performance and competitiveness of conventional Fenton by ensuring higher availability of iron catalyst while minimizing sludge production.

Synthesis of 5-hydroxymethylfurfural from glucose, fructose, cellulose and agricultural wastes over sulfur-doped peanut shell catalysts in ionic liquid.

In this study, waste peanut shells were sulfur-impregnated and used as acid catalysts in the presence of an ionic liquid for the conversion of fructose, glucose, and cellulose into 5-hydroxymethylfurfural, a useful chemical intermediate for biofuel production. Effects of sulfur-doping duration (1 h and 5 h), solvent type and proportion, reaction temperature (130 °C, 140 °C, and 150 °C), time (30-240 min), catalyst-to-substrate ratio (1-2.5 m/m), and agricultural residue (peanut shell, Canada wheat straw, water hyacinth, stalk, and reed) on HMF yields were investigated. Monophasic and biphasic ionic liquids such as [amim]Cl, [bmim]HSO4, and [emim]Cl were employed in combination with choline chloride and dimethyl sulfoxide to improve HMF yields. Results show that peanut shells subjected to prolonged sulfur impregnation produced higher HMF yields. At 130 °C and 2 h, HMF yields from fructose and glucose reached 94.6% and 55.1%, respectively. Higher reaction temperatures improved HMF yields and accelerated conversion rates for the sugar substrates. Moreover, HMF production from waste biomass namely, peanut shells, peanut stalk, Canadian wheat straw, reed, and water hyacinth were examined in separate one-pot catalytic reactions. Overall, the study showed the effectiveness of sulfur-doped peanut shells as solid acid catalysts for the synthesis of HMF from various sources and the results may be used in designing large-scale production of furanic biofuel precursors from agricultural wastes.