RESUMO
In this work, an effort has been made to enhance the efficacy of biological process for the effective degradation of 2, 4-dichlorophenol (2, 4-DCP) from wastewater. The polyurethane foam was modified with Fe3O4 nanoparticles and combined with polyvinyl alcohol, sodium alginate, and bacterial consortium for biodegradation of 2, 4-DCP in a packed bed biofilm reactor. The maximum removal efficiency of 2, 4-DCP chemical oxygen demand, and total organic carbon were found to be 92.51 ± 0.83 %, 86.85 ± 1.32, and 91.78 ± 1.24 %, respectively, in 4 days and 100 mg L-1 of 2, 4-DCP concentration at an influent loading rate of 2 mg L-1h-1 and hydraulic retention time of 50 h. Packed bed biofilm reactor was effective for up to four cycles to remove 2, 4-DCP. Growth inhibition kinetics were evaluated using the Edward model, yielding maximum growth rate of 0.45 day-1, inhibition constant of 110.6 mg L-1, and saturation constant of 62.3 mg L-1.
Assuntos
Biodegradação Ambiental , Biofilmes , Reatores Biológicos , Clorofenóis , Poliuretanos , Poliuretanos/química , Biofilmes/efeitos dos fármacos , Cinética , Poluentes Químicos da Água , AnimaisRESUMO
Integratingphotocatalysisand biodegradation has shown great potential in wastewater treatment technology. In this study, the degradation of p-cresol in water has been investigated through an integrated system comprising of photocatalytic and packed bed biofilm reactor (PBBR). In the photocatalytic reactor, the biodegradability index (BOD5/COD, BOD5/TOC) of the p-cresol solution was first shown to increase (from 0.098±0.023 to 0.59±0.089 for BOD5/COD and from 0.27±0.030 to 1.74±0.03 for BOD5/TOC). The pseudo-first-order rate constant (kap) was found to be 0.011 min-1. The % removal of the integrated system was found to be 98.43±1.31% at an initial concentration of 700 mg L-1 and residence time of 120 h, which was significantly higher than the PBBR operated alone (34.82±2.62%) under optimized conditions (pH 7.0 and T = 32±2 °C). Using an integrated approach, the efficient removal of p-cresol opens novel future perspectives for catalytic degradation using chemical oxidation.