The treatment and reuse of domestic wastewater using an anaerobic baffled reactor (ABR) followed by a duckweed pond (DWP) were the main theme of the present study. The ABR was fed continuously with domestic wastewater at four HRTs ranging from 8 to 24 h and corresponds to organic loading rates ranging from 0.67 to 2.1 kg COD/m³/day. The ABR effluent was fed to a DWP operating at 10 and 15 days. The performance of the ABR at the four HRTs gave satisfactory results. Chemical oxygen demand (COD) removal was between 68 and 82%. Fecal coliform removal was between 1 to 2 logs. The 12- and 18-h hydraulic retention times (HRTs) gave close results, as indication of the possible selection of the 12-h HRT as the optimum operation for the ABR based on economic advantage. The ABR compartmentalized structure gave results higher than those produced by the one-stage digester and similar to those produced by the two-phase anaerobic digestion process. Duckweed ponds as post-treatment operated at 10 days and 15 days gave the best results at 15-day HRT, where it was possible to remove 73.4% of nitrogen and 65% of phosphorus and produce protein-rich dry duckweed of 105 kg/ha/day on average. The removal of fecal coliform (FC) in duckweed ponds was 3–4 logs. The final treated domestic sewage characteristics proved its compliance with the Egyptian standards for reuse in restricted irrigation.

A precise, Eco-friendly, and highly sensitive RP-HPLC method was employed using quality-by-design principles to concurrently identify cephalexin and cefixime residues in the manufacturing machines using a hypersil BDS C18 column (250 × 4.6 mm, 5 μm) at wavelength 254 nm. The Box–Behnken design was applied to obtain the best chromatographic conditions with the fewest possible trials. Three independent factors viz organic composition, flow rate, and pH were used to assess their effects on the responses' resolution and retention time. Overlay plot and desirability functions were implemented to predict responses of the high resolution and relatively short retention time using a mobile phase composed of acidic water: acetonitrile (85:15, v/v) at pH 4.5 adjusted by phosphoric acid with a flow rate of 2.0 mL/min. The spectral overlapping of the drugs was successfully resolved by the mean centering ratio (MCR) spectra approach at 261 nm and 298 nm for cephalexin and cefixime, respectively. Good linearity results were obtained for the suggested HPLC and MCR methods over the concentration range of (0.05–10 ppm) and (5–30 ppm) with a detection limit of 0.003, 0.004, 0.26, and 0.23 ppm, and quantitation limits of 0.008, 0.013, 0.79, and 0.68 ppm for cephalexin and cefixime, respectively, with a correlation coefficient of ≥ 0.9998 and good swab recovery results of 99–99.5%. A process capability index was accomplished for chemical and micro results, illustrating that both are extremely capable. The suggested method was effectively validated using ICH recommendations.

Economical, highly robust, selective, precise, and eco-friendly RP-UPLC and spectrophotometric methods were developed and validated for the concurrent estimation of selected pharmaceutical drugs represented in ceftazidime (CFZ) and pyridine (PYD) in their solutions using Agilent Zorbax SB-C18 RRHD (50 × 2.1 mm, 1.8 μm) column at flow rate 0.3 mL/min with wavelength 254 nm. Box-Behnken design (BBD) established Response surface methodology (RSM) to achieve the optimum chromatographic condition with minimal trials conducted. Three independent variables specifically acetonitrile ratio 60–70%, pH 3–7, and temperature 25–35 °C were implemented to evaluate the influences of these variables on the responses as resolution and retention time. Desirability and overlay plots were carried out to adjust the optimal condition that achieved the shortest retention time of less than 2 min and desired resolution of more than 1.5 using a mobile phase consisting of acetonitrile: purified water (70:30, v/v) at pH 5.0 adjusted by 0.1% orthophosphoric acid with the column oven temperature 30 °C and column void volume 0.46 mL. Mean centering of ratio spectra (MCR) and ratio subtraction (RS) methods were effectively applied to resolve drugs' spectral superposition at 220 nm, 255.4 nm, 260.3 nm, and 254.6 nm for CFZ and PYD, respectively. Linearity range was accomplished for UPLC, MCR, and RS methods over the concentration range of 2–100, 1–50,3–30 and 5–30 µg/mL for CFZ and PYD, respectively with correlation coefficient > 0.999 and good recovery results within 98–102%. Six Sigma methodology was achieved using the process capability index (Cpk) to compare the suggested and USP methods showing that both are highly capable with Cpk > 1.33. The proposed method was successfully validated depending on ICH guidelines and ANOVA results and applied for the accelerated stability study. Graphical Abstract

It has been reported that spinal deformity was induced in developing fish by the addition of polycyclic aromatic hydrocarbons (PAHs). To examine the mechanism of the disruption of fish bone metabolism, the effect of benz[a]anthracene (BaA), a kind of PAH, on plasma calcium, inorganic phosphorus, osteoblasts, and osteoclasts was investigated in this study. We also measured several plasma components to analyze the toxicity of BaA on other metabolisms. BaA (1 or 10 ng/g body weight) was intraperitoneally injected (four times) into nibbler fish during breeding, for 10 days, and it was indicated, for the first time, that injecting high doses of BaA to nibbler fish induced both hypocalcemia and hypophosphatemia. Furthermore, in the scales of nibbler fish treated with high doses of BaA, both osteoclastic and osteoblastic marker messengerRNA (mRNA) expressions decreased. These results are a cause of disruption of bone metabolism and, perhaps, the induction of spinal deformities. In addition, we found that total protein, metabolic enzymes in the liver, total cholesterol, free cholesterol, and high-density lipoprotein cholesterol levels significantly decreased in BaA-injected fish. These results indicate that BaA may affect liver diseases and emphasize the importance of prevention of aquatic PAH pollution.

Throughout the industrial activities, water consumption is increased, resulting in large amounts of wastewater that must be treated before being discharged into the water streams. Coagulation/flocculation and sedimentation processes are considered as one of the most used chemical treatment methods for removing the majority of water contaminants. Cationic dye of methylene blue (MB) and anionic dye of methyl orange (MO) are common hazardous organic wastewater contaminants that mostly degraded by different chemical coagulants processes. Chemical coagulants act as an auxiliary agent in the coagulation/flocculation-sedimentation process. This study aimed to investigate the effectiveness of combined chemical coagulants of FeCl3/lime in the degradation of cationic and anionic dyes. In this work, kinetics, effect of adsorption parameters such as pH, initial concentration of dyes and the chemicals coagulants doses was studied. At an optimum coagulant dosage of (200/70) mg/L and (70/100) mg/L, and optimum pH ranged from (6.0 - 8.0) for MO and MB, repectively . The achieved removal values for both anionic and cationic dyes using the combined coagulant (FeCl3/lime) were 97.78% and 95.54% for MO and MB, respectively. The maximum adsorption capacity of FeCl3/ lime was calculated from the isotherm at 500 mg/g. This technique was successfully conducted for the treatment of tannery and laundry wastewaters for improving the quality of pollution parameters and investigating the efficiency of the applied treatment technique. The achieved removal efficiencies for tannery and laundary wastewater ranged from 93.9 to 94.4 % for COD, 92.9 to 92.5% for BOD5 , 93.7 to 92.8% for TSS, and 96.7 to 99.2% for turbidity, respectively.