Adsorption and removal of cadmium ions from simulated industrial wastewater using hydrophilic and hydrophobic commercial silica nanoparticles are reported. These results are compared with those obtained using sol–gel silica nanoparticles. Two types of dense commercial pyrogenic silica nanoparticles with different chemical groups on the surface were used to adsorb cadmium ions: Aerosil A130VS and R972. The pore absence in these particles reduces the surface area and, consequently, the concentration of active chemical groups appropriated for adsorption, as compared with the sol–gel particles that are highly porous; this effect is partially compensated by the small sizes available for these commercial particles. The concentration of cadmium ions was reduced: from 109 to 0.01 ppm for A130VS, from 138 to 1.44 ppm for R972, and from 123 to 0.005 ppm for sol–gel. The flocculation kinetics was obtained using dynamic light scattering and the amount of adsorbed cadmium in the sediment using atomic absorption spectroscopy.

Chromium(III) oxide is an amphoteric, dark green solid. This most stable dye is widely used in construction and ceramic industries as well as in painting. In this study, the attempt is made to determine flocculating properties of exopolysaccharide (EPS) synthesized by the bacteria Sinorhizobium meliloti 1021, which would increase the efficiency of chromium(III) oxide removal from sewages and wastewaters. The conditions under which EPS is the most effective destabilizing component of chromium(III) oxide suspension have been determined too. In order to characterize the structure of electric double layer formed at the solid/supporting electrolyte (EPS) solution interface, electrokinetic potential measurements and potentiometric titration were performed. The EPS amount adsorbed on the chromium(III) oxide surface as a solution pH function was also measured. Moreover, the stability of Cr₂O₃suspension in the absence and presence of S. meliloti 1021 EPS was estimated. The pooled analysis of all obtained results showed that EPS causes chromium(III) oxide suspension destabilization in the whole examined pH range. The largest change in the system stability before and after the polymer addition was observed at pH 9. It is probable that under these conditions bridging flocculation occurs in the examined system.

Extracellular polymeric substances (EPS) are an extracellular matrix found in sludge which plays a crucial role in flocculation by interacting with the organic solids. Therefore, to enhance pretreatment of sludge, EPS have to be removed. In this study, EPS were removed with a chemical extractant, NaOH, to enhance the bacterial pretreatment. A lysozyme secreting bacterial consortium was isolated from the waste activated sludge (WAS). The result of density gradient gel electrophoresis (DGGE) analysis revealed that the isolated consortium consists of two strains. The two novel strains isolated were named as Jerish03 (NCBI accession number KC597266) and Jerish 04 (NCBI accession number KC597267) and they belong to the genus Bacillus. Pretreatment with these novel strains enhances the efficiency of the aerobic digestion of sludge. Sludge treated with the lysozyme secreting bacterial consortium produced 29 % and 28.5 % increase in suspended solids (SS) reduction and chemical oxygen demand (COD) removal compared to the raw activated sludge (without pretreatment) during aerobic digestion. It is specified that these two novel strains had a high potential to enhance WAS degradation efficiency in aerobic digestion.

The treatment of a non-biodegradable agrochemical wastewater has been studied by coupling of preliminary coagulation—flocculation step and further Fenton oxidation. High percentages of chemical oxygen demand (COD) removal (up to 58 %) were achieved in a first step using polyferric chloride as coagulant. This reduced significantly the amount of H₂O₂ required in the further Fenton oxidation. Using the stoichiometric amount relative to COD around 80 % of the remaining organic load was mineralized. The combined treatment allowed achieving the regional discharge limits of ecotoxicity at a cost substantially lower than the solution used so far where these wastewaters are managed as hazardous wastes.

Modern society grapples with large amounts of household waste. The anaerobic digestion of this waste offers a promising source for energy-rich biogas production but generates high toxic effluents that require treatment before reuse or disposal into the environment. This study aimed to investigate three techniques, namely coagulation/flocculation, electro-coagulation, and activated sludge, in terms of efficiency in the treatment of these effluents. It also aimed to assess their toxicity effects on the germination and growth of durum wheat Triticum aestivum L. seeds before and after 6 days of treatment. Activated sludge was most efficient in reducing chemical oxygen demand, turbidity, and conductivity (95.7 %, 15.8 %, and 37.5 %, respectively). The effluent treated with this technique induced a marked delay in germination (low mean time of germination) and a significant reduction in the percentages of seed germination and root and leaf growths. It was also noted to strongly induce lipid peroxidation in roots and leaves, which presumably explained the germination/growth inhibition of the wheat seeds. The effluent also induced marked lipid peroxidation effects and strongly inhibited the activities of butyrylcholinesterase in mice bone marrows. The effluent shows a high ability to inhibit the growth of three microalgae; these endpoints are useful tools to biomonitor the physico-chemical quality of this wastewater. Overall, while no significant alterations were observed in terms of animal and vegetable toxicities when the effluent was treated by coagulation/flocculation, activated sludge treatment proved efficient in reducing the toxicities induced by the untreated effluents. The results indicate that the application of this technique is promising with regards to attaining efficient, eco-friendly, and cost-effective strategies for the management and treatment of household waste.

A new inorganic-organic hybrid material zirconium-glycine complex (ZGC) was firstly used as a coagulant in a coagulation process to treat Pearl River raw water. Its coagulation performance was compared with commonly used aluminum (Al) coagulants such as aluminum sulfate (Al₂(SO₄)₃) and polyaluminum chloride (PAC), in terms of water quality parameters and floc properties. ZGC coagulation achieved higher removal of turbidity (93.8 %) than other traditional coagulants. Charge neutralization was proven to act as a dominant mechanism during ZGC coagulation. The aggregated flocs with ZGC showed the fastest growth rate and good recovery ability compared with the other coagulants and achieved the largest floc size within 5 min. The ZGC coagulant can decrease the hydraulic retention time and increase removal efficiency.

The coking wastewater generally comprises highly concentrated, recalcitrant, and toxic organic pollutants, so its treatment has been of great importance to prevent living beings and their environment from these hazardous contaminations. The treatment of pretreated coking wastewater by flocculation-coagulation, alkali out, air stripping, and three-dimensional (3-D) electrocatalytic oxidation was performed (gap between the used β-PbO₂/Ti anode and titanium cathode, 12 mm; mass ratio of Cu-Mn/granular activated carbon (GAC) to effluent, 1:4; cell voltage, 7 V). The results showed that the pH adjusting from 3.7 to 6.1 was necessary for coagulants; alkali out played an important role because it brought up precipitation containing higher fatty acids as well as other contaminants to decrease the chemical oxygen demand (COD) in the effluent, and it had also forced the reduction of ammonia nitrogen (NH₃-N) by incorporating with air stripping; for 3-D electrocatalytic oxidation with a bleaching liquid assisting, the initial pH 8.5 of effluent was suitable for Cu-Mn/GAC; moreover, it was considered that its Cu component was dedicated to the decrease of COD and NH₃-N, while the Mn component specialized in the decay of NH₃-N. The residual COD and NH₃-N values in the final effluent with pH 6.5 were 95.8 and 8.8 mg/L, respectively, demonstrating that the whole processes applied were feasible and low in cost.