This paper reports on the process of industrial-type wastewater purification carried-out through continuous anodic dissolution of aluminum alloy sacrificial anode for artificially aerated Cu-Al alloy galvanic (macro-corrosion) cells and synthetically prepared wastewater solutions. Electrochemical experiments were performed by means of a laboratory size electrolyzer unit, where the electrocoagulation process along with surface-induced electrooxidation phenomena were examined for wastewater containing Acid Mixture and Disperse Red 167 dyes. Final reduction of the dyes concentrations came to 32 and 99% for Acid Mixture and Disperse Red 167, correspondingly. The above was visualized through the employment of electrochemical (cyclic voltammetry and a.c. impedance spectroscopy techniques) and instrumental spectroscopy analyses.

This work is a review of scientific papers on the influence of temperature (T) on the biosorption of various dyes from aqueous solutions and wastewaters. The dyeing process of textiles is usually carried out at high temperatures, and therefore, the wastewater generated there when entering the treatment plant may still be hot. Hence, depending on the climatic conditions of a given region, the biosorption method used for their purification may occur at various temperatures. Most of the papers clearly stated the positive influence of T on biosorption, generally indicating the chemical nature of this process. At the same time, substantial number of authors confirmed the positive effect of T on the biosorption with an initial T-rise from approximately 20 °C to about 30–40 °C range; conversely, at higher temperatures, they indicated a decrease in the biosorption efficiency. Additionally, many authors clearly implied the negative impact of T on the biosorption parameters. They generally envisaged the physical nature of this process, but also indicated its limitation, as there was only a 15%–50% reduction in biosorption efficiency with an increase in T. In addition, an attempt was made to analyse the effect of temperature on the biosorption process, depending on the type of dye. It could then be cautiously suggested that a moderate increase in the T parameter favourably affected the biosorption of the red and reactive dyes.

Municipal wastewater sludge was produced by chemical coagulation of synthetic wastewater (sww) based on Synthene Scarlet P3GL disperse dye and real municipal wastewater (nww), coagulated by commercial coagulants PAX (prepolymerised aluminum coagulant) and PIX (a ferric coagulant based on Fe₂(SO₄)₃). An attempt was made to correlate the sludge’s dewatering capacity (in terms of capillary suction time—CST) with operation parameters for wastewater treatment, size distribution and specific surface area of the sludge particles. It was found that the presence of phosphate ions in the system facilitates the removal efficiency of the above-mentioned dye (L) due to the interaction between the dye molecules and H₂PO₄⁻ ions. Unlike sww, negatively charged organic substances (sorg) in nww are directly adsorbed on the surface of colloidal particles {Fe(OH)₃} and {Al(OH)₃} (prtc). It was also discovered that an increase in the dose of a coagulant led to an increase of CST for sww sludge and to a decrease of CST for nww sludge. It has been suggested that flocs composed of spherical {Al(OH)₃} units possessed more internal space for water than aggregates consisting of rod-shaped {Fe(OH)₃} units and, consequently, it is more difficult to remove water from Al-sww sludge than from Fe-sww. The results obtained showed that smaller particles dominate in sww sludge, while larger particles are prevalent in nww sludge. To explain this distinct difference in the size distribution of particles in sludge obtained with the use of Al³⁺ and Fe³⁺, simple models of aggregation and agglomeration-flocculation processes (aaf) of treated wastewater have been proposed. Except for PIX in nww, the analyzed particles of the investigated types of sludge were characterized by similar specific surface area (Sps), regardless of the kind of sludge or the applied coagulant. Slightly larger, negatively-charged sorg bridges, anchored directly on the surface of positive prtc are more effective in closing the structure of nww sludge than small L bridges of the dye molecules anchored on the surface of prtc via H₂PO₄⁻. All the discovered aspects could lead to improved performance of wastewater treatment plants (WWTP) by increasing the efficiency of sludge dewatering.

This work reports on the kinetics of electrochemical degradation of the resorcinol molecule, examined on nickel foam-based electrodes in contact with 0.1 M NaOH and 0.5 M Na₂SO₄ supporting electrolytes. The electrooxidation of resorcinol was examined on as-received, as well as on Pd-modified, nickel foam catalyst materials, produced via spontaneous deposition of trace amounts of palladium element. Electrochemical (cyclic voltammetry and a.c. impedance) experiments were carried out by means of a three-compartment, pyrex glass electrochemical cell, whereas continuous resorcinol electrooxidation tests were conducted galvanostatically (or potentistatically) with a laboratory-size, single-cell electrolyzer unit. In addition, quantitative determination of resorcinol and its possible electrodegradation products was performed by means of instrumental HPLC: High-Performance Liquid Chromatography/MS: Mass Spectrometry methodology. Also, SEM (Scanning Electron Microscopy) and EDX (Energy Dispersive X-ray spectroscopy) techniques were employed for Ni foam (Pd-modified Ni foam) surface characterizations.

This study compares the effectiveness of pollutant removal from synthetic dairy wastewater electrocoagulated by means of aluminum and iron anodic dissolution. A method based on the cubic function (third degree polynomial) was proposed for electrocoagulant dosing. Mathematical methods for calculating the optimal electrocoagulant doses proved to be quite precise and useful for practical applications. The results of gravimetric measurements of electrocoagulant (electrode) consumption demonstrated that theoretical doses of Al determined based on Faraday's law were substantially lower than those produced by electrode weighing. The above phenomenon was also discussed in the light of the results of polarization resistance measurements for Al and Fe electrodes used in the study.

Electrocoagulation makes an alternative method to chemical coagulation. This paper presents the results obtained during the electrocoagulation of the model wastewater using aluminum electrodes. The wastewater was treated by means of chronopotentiometric electrocoagulation process in a static system, at the constant current I = 0.3 A; therefore higher doses of electrocoagulant required longer electrocoagulation time. Changes in zeta potential, pH, turbidity, chemical oxygen demand (COD), suspended solids and total phosphorus concentrations in the treated wastewater were determined. A new method for determining the optimal dosage of the aluminum electrocoagulant was proposed through application of the third degree polynomial function rather than the parabolic equation. An increase in the electrocoagulant dose raised the share of sweep fl occulation in the studied treatment process, resulting in the effective removal over 90% of phosphorus compounds from the system.