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In an era of increasing environmental awareness, it is very important to work towards eliminating or at least reducing as many harmful industrial substances as possible. However, the implementation of green chemistry methods for wastewater treatment can be difficult especially due to complexity, the high cost of reagents, and the required long process time. This paper focuses on using waste iron (WI) to remove two kinds of amaranth dye commonly used in industry. To enhance the process, UV irradiation and hydrogen peroxide were used. The novelty of the research was the use of efficient and reusable WI as a heterogeneous catalyst in the process. WI material characteristics was done before and after the process using scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), and X-ray fluorescence (XRF). Zeta potential, size characterization, circularity, and direct band gap were also determined. As a result of treatment complete decolorization of both dyes was achieved, as well as 99% absorbance removal after 15-min process time. The total organic carbon (TOC) decrease after 60-min process time was in the range from 86.6 to 89.8%. Modified pseudo-second-order reaction reflects obtained results of treatment efficiency. Treatment results, confirmed by WI material characterization, indicate satisfactory stability of the catalyst and good oxidation capacity.

Rapid global industrialization constantly impacts the environment by discharging pollutants. Therefore, various materials are currently being investigated for environmental applications, including two-dimensional (2D) MXenes. Herein, we focus on MXene-enabled technologies for removing inorganic and organic contaminants present in gaseous and liquid forms, especially organic dyes, pharmaceuticals, and solid pollutants. We foresee a considerable potential for MXene-enabled technologies to remove heavy ions and radionuclides and recover precious elements. We show that MXenes could efficiently inactivate microorganisms without harming the environment. Finally, we discuss the associated opportunities and challenges in MXenes’ surface chemistry, semiconducting activity, interfacial effects, adsorption, and photocatalysis. Altogether, this article showcases outstanding opportunities for MXenes in the rapidly growing field of environmental applications. Graphical abstract

Background: There is a need for more effective methods of industrial wastewater treatment. Methods: Cosmetic wastewater was collected and subjected to H2O2/Fe3O4/Fe2O3/Fe0 and UV/H2O2/Fe3O4/Fe2O3/Fe0 process treatment. Results: Total organic carbon (TOC) was decreased from an initial 306.3 to 134.1 mg/L, 56.2% TOC removal, after 120 min of treatment for 1:1 H2O2/COD mass ratio and 500/500/1000 mg/L Fe3O4/Fe2O3/Fe0 catalyst doses. The application chromatographic analysis allowed for the detection and identification of pollutants present in the wastewater. Identified pollutants were removed during the treatment processes. Processes carried out at a pH greater than 3.0 were ineffective. The UV process was more effective than the lightless process. Conclusions: The applied processes are effective methods for wastewater treatment. Chromatographic results confirmed the effectiveness of the treatment method. The kinetics of the process were described by the modified second-order model. On the basis of ANOVA results, the hypothesis regarding the accuracy and reproducibility of the research was confirmed.

Wastewater from a cosmetic factory, with an initial total organic carbon (TOC) of 146.4 mg/L, was treated with Fe2O3/Fe0/H2O2, Fe3O4/Fe0/H2O2, light/Fe2O3/Fe0/H2O2, and light/Fe3O4/Fe0/H2O2 processes. The light-supported processes were more effective than the lightless processes. The fastest TOC removal was observed during the first 15 min of the process. Out of the four tested kinetic models, the best fit was obtained for the modified second-order reaction with respect to the TOC value. The best treatment efficiency was obtained for the light/Fe3O4/Fe0/H2O2 process with 250/750 mg/L Fe3O4/Fe0 reagent doses, a 1:1 hydrogen peroxide to Chemical Oxygen Demand (H2O2/COD) mass ratio, and a 120 min process time. These conditions allowed 75.7% TOC removal to a final TOC of 35.52 mg/L and 90.5% total nitrogen removal to a final content of 4.9 mg/L. The five-day Biochemical Oxygen Demand to Chemical Oxygen Demand (BOD5/COD) ratio was increased slightly from 0.124 to 0.161. Application of Head Space Solid-Phase Microextraction Gas Chromatography Mass Spectrometry (HS-SPME-GC-MS) analysis allows for the detection and identification of 23 compounds contained in the raw wastewater. The identified compounds were eliminated during the applied process. The HS-SPME-GC-MS results confirmed the high efficiency of the treatment processes.