Sustainable indigenous bio-mixture for restoration the soil point source pollution with special reference to chlorpyrifos.

Improper pesticide handling is the main cause of contamination of the environment in agricultural systems. This could be caused by leakage of spraying liquid, leftovers, and inappropriate washing of spraying equipment. This study assessed the ability of suggested biomixture modules for remediate repetitive cycles of high chlorpyrifos doses. In three consecutive treatments, four tested modules were contaminated with 160 µg g-1 chlorpyrifos. Chlorpyrifos residues, dehydrogenase activity, and microbial respiration were continuously monitored for 22 weeks. Six bacterial consortia were isolated at the end of the experiment from four treated modules (B+3, BF+3, S+3, and SF+3) and two from untreated modules (B and S). The isolated consortium efficiency in degrading chlorpyrifos was studied. The results revealed that the best chlorpyrifos removal efficiency was achieved when using the stimulated biomixture module (BF) recorded 98%, 100%, and 89%, at the end of three chlorpyrifos treatments, respectively. Such removal efficiency was compatible with the biological activity results of the tested modules: dehydrogenase activity and microbial respiration. There was no difference in the efficiency among the S, B, and BF+3 consortia. The results presented here demonstrate that the combination of vermicompost, wheat straw, soil, and NPK (stimulated biomixture module) can successfully reduce the risk of a point source of pesticide pollution.

Influences of Mg-activation on sugarcane bagasse biochar characteristics and its PNP removing potentials from contaminated water.

Biochar as a substitute eco-friendly and low-cost adsorbent is introduced for removing p-nitrophenol (PNP) one of the most important chemical contaminant that recognized as the main metabolite in many pesticides and an intermediate compound in many industries. Physicochemical characteristics of sugarcane bagasse biochar (SCBB) and its Mg-activation (ASCBB) generated at 500 °C for 30 min were investigate. Batch kinetic experiment was conducted (200 mg L-1 PNP) to evaluate sorption efficiency of both tested biochars. To study the reaction behavior of PNP adsorption on ASCBB, solution pH and isotherm experiment of different concentrations and dosages were as investigated. The results show that ASCBB had a higher biochar yield, ash content, pH, molar ratios (H/C and O/C), surface area, pore volume, mean pore diameter, and specific and thick wall structure than SCBB. The efficiency of ASCBB to remove PNP was higher than SCBB which reached 51.98% in the first 1 min., and pH 7 achieved the optimum adsorption. Pseudo-second-order model examination exhibited well fitted to explain the adsorption results depending on R2 value (1.00). The adsorption isotherm results were well described by the Elovich and Freundlich models depending on the R2, qm and n values, which means the formation of a multilayer of PNP on the ASCBB surface through the chemisorption reaction. The calculated qm (144.93 mg g-1) of 1g L-1 was relatively close with experimental value (142.03 mg g-1). The PNP adsorption mechanism on both biochar types was electrostatic attraction, hydrogen bonding, and π-π stacking interactions, which were confirmed by studying the surface reactions before and after adsorption. Overall, the current study provided a successful waste biomass-derived biochar as a conducive alternative eco-sorbent to eliminate p-nitrophenol from wastewater.