A critical review of textile industry wastewater: green technologies for the removal of indigo dyes.

The denim textile industry represents an important productive sector. It generates wastewater with low biodegradability due to the presence of persistent pollutants, which can produce toxic and carcinogenic compounds; therefore, wastewater treatment reduces risks to aquatic life and public health. This paper presents a review of 172 papers regarding textile industry wastewater treatment for the removal of contaminants, especially indigo dyes used in the denim industry, in the context of green technologies. The physicochemical characteristics of textile wastewater, its environmental and health impacts, and the permissible limit regulations in different countries were reviewed. Biological, physicochemical and advanced oxidation processes for the removal of indigo dyes were reviewed. The goal of this study was to analyze the characteristics of green technologies; however, the research does not clearly demonstrate an effect on energy consumption savings, carbon footprint decreases, and/or waste generation. Advanced oxidation processes showed the highest color removal efficiency (95 and 97% in synthetic or real wastewater, respectively). Photocatalysis and Fenton reactions were the most efficient processes. None of the revised works presented results regarding upscaling for industrial application, and the results should be discussed in terms of the guidelines and maximum permissible limits established by international legislation. New technologies need to be developed and evaluated in a sustainable context with real wastewater.

Toward more sustainable photovoltaic solar electrochemical oxidation treatments: Influence of hydraulic and electrical distribution.

Powering electrochemical technologies with renewable energies is a promising way to get more sustainable environmental remediation techniques. However, the operational conditions of those processes must be optimized to undergo fast and efficient treatments. In this work, the influence of electrical and hydraulic connections in the performance of a set of two electrolyzers directly powered by photovoltaic panels was evaluated. Despite both electrolyzers were assembled using the same electrode material, they showed different performances. Results indicate that the electrolyzer with higher ohmic resistance and higher overpotential attained a greater production of oxidant species, being produced under the most efficient strategy around 4.8 and 15.1 mmol of oxidants per Ah by electrolyzer 1 and 2, respectively. Nevertheless, an excess of oxidant production because of an inefficient energy management, led to low removal efficiencies as a consequence of a waste of energy into undesirable reactions. Regarding the hydraulic distribution of wastewater between the cells, it was found to influence on the total remediation attained, being the serial connection 2.5 and 1.8 more efficient than a parallel wastewater distribution under series and parallel electrical strategies, respectively. Regarding electrical strategies, parallel connections maximize the use of power produced by the photovoltaic panels. Furthermore, this allows the system to work under lower current densities, reducing the mass transfer limitations. Considering both advantages, a hydraulic connection of the cells in series and an electrical connection in parallel was found to reach the highest specific removal of pollutant, 2.52 mg clopyralid (Wh)-1. Conversely, the opposite strategy (parallel hydraulic connection-series electrical connection) showed the lowest remediation ratio, 0.48 mg clopyralid (Wh)-1. These results are important to be considered in the design of electrolytic treatments of waste directly powered by photovoltaic panels, because they show the way to optimize the cells stack layout in full-scale applications, exhibiting significant impact on the sustainability of the electrochemical application.

Comparison of Fe-Al-modified natural materials by an electrochemical method and chemical precipitation for the adsorption of F- and As(V).

The adsorption of fluoride and arsenic ions by modified natural materials may have an impact on the removal of F- and As(V) from waters. In this work, a zeolitic material and pozzolan (commonly known as pumicite) were modified with aluminium an iron by an electrochemical method and chemical precipitation, respectively. The adsorbents were characterized by X-ray diffraction, scanning electron microscopy with energy X-ray disperse spectroscopy analysis and the point of zero charge (pHzpc). F- and As(V) adsorption properties of both materials were investigated. Adsorption kinetic data were best fitted to pseudo-second-order model and equilibrium data to the Langmuir isotherm model. The highest F- and As(V) sorption capacities were obtained for modified zeolitic (0.866 mg/g) and pozzolan (3.35 mg/g) materials, respectively, with initial F- or As(V) concentrations of 10 mg/L. It was found that the unmodified materials did not show either adsorption of F- ions or As(V), which indicated that Al and Fe in the adsorbents are responsible for the adsorption of these ions. In general, both modified materials show similar capacities for the adsorption of F- and As(V).

Comparison of aluminum modified natural materials in the removal of fluoride ions.

The removal behaviors of fluoride ions from aqueous solutions and drinking water by aluminum modified hematite, zeolitic tuff and calcite were determined. Drinking water containing naturally 8.29 mg of fluoride ions per liter was characterized. The hematite, zeolitic tuff and calcite were aluminum modified by an electrochemical method. The effects of contact time and the dose of adsorbent were determined. The PZC (point of zero charge) values for aluminum modified hematite, zeolitic tuff and calcite were 6.2, 5.8 and 8.4, respectively. Adsorption kinetic data were best fitted to pseudo-second-order and Elovich models and equilibrium data to Langmuir-Freundlich isotherm model. The highest fluoride sorption capacities (10.25 and 1.16 mg/g for aqueous solutions and drinking water respectively) were obtained for aluminum modified zeolite with an adsorbent dosage of 10 g/L and an initial F(-) concentration of 9 and 8.29 mg/L for aqueous solutions and drinking water respectively (the final concentrations were 0.08 and 0.7 mg/L respectively). The main mechanism involved in the adsorption of fluoride ions is chemisorption on heterogeneous materials according to the results obtained by fitting the data to kinetic and isotherm models respectively. Aluminum modified zeolitic tuff showed the best characteristics for the removal of fluoride ions from water.

Biosorption of Cr(III) and Fe(III) in single and binary systems onto pretreated orange peel.

Trivalent chromium and iron are the products of the traditional reduction of hexavalent chromium by ferrous salts in industrial wastewater. Although there have been a few studies of Cr(III) adsorption, none have considered the effect of Fe(III) on Cr(III) adsorption in a binary system representing expected products of hexavalent chromium in industrial wastewater. The biosorption of Cr(III) and Fe(III) ions onto pretreated ground orange peel in single and binary systems was studied in batch experiments using a variety of techniques. The kinetic results showed a rapid rate of biosorption of Cr(III) and Fe(III) in single and binary systems and mutual interference effects in the competitive binary Cr(III)-Fe(III) system. Second order kinetic models showed the best fit for all systems. The behavior of competitive Cr(III)-Fe(III) biosorption were successfully described by the multicomponent Langmuir model, obtaining maximum capacities for Cr(III) and Fe(III) of 9.43 and 18.19 mg/g respectively. SEM/EDS results confirmed that the metals adsorb on the surface and FTIR identified the hydroxyl groups on the carboxylic acids as the active binding sites.