In this age, a key target for enhancing the competitiveness of the chemical, environmental and biotechnology industries is to manufacture high-value products more efficiently and especially with significantly reduced environmental impact. Under this premise, the conversion of biomass waste to a high-value added product, biochar, is an interesting approach under the circular economy principles. Thus, the improvements in the biochar production and its new and innovative uses are hot points of interest, which are the focus of vast efforts of the scientific community. Biochar has been recognized as a material of great potential, and its use as an adsorbent is becoming a reliable strategy for the removal of pollutants of different streams, according to its high adsorption capacity and potential to eliminate recalcitrant compounds. In this review, a succinct overview of current actions developed to improve the adsorption capability of biochar, mainly of heavy metal and organic pollutants (dyes, pharmaceuticals and personal care products), is summarized and discussed, and the principal adsorption mechanisms are described. The feedstock and the production procedure are revealed as key factors that provide the appropriate physicochemical characteristics for the good performance of biochar as an adsorbent. In addition, the modification of the biochar by the different described approaches proved their feasibility and became a good strategy for the design of selective adsorbents. In the last part of this review, the novel prospects in the regeneration of the biochar are presented in order to achieve a clean technology for alleviating the water pollution challenge.

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Nowadays, the contamination of wastewater by organic persistent pollutants is a reality. These pollutants are difficult to remove from wastewater with conventional techniques; hence, it is necessary to go on the hunt for new, innovative and environmentally sustainable ones. In this context, advanced oxidation processes have attracted great attention and have developed rapidly in recent years as promising technologies. The cornerstone of advanced oxidation processes is the selection of heterogeneous catalysts. In this sense, the possibility of using metal–organic frameworks as catalysts has been opened up given their countless physical–chemical characteristics, which can overcome several disadvantages of traditional catalysts. Thus, this review provides a brief review of recent progress in the research and practical application of metal–organic frameworks to advanced oxidation processes, with a special emphasis on the potential of Fe-based metal–organic frameworks to reduce the pollutants present in wastewater or to render them harmless. To do that, the work starts with a brief overview of the different types and pathways of synthesis. Moreover, the mechanisms of the generation of radicals, as well as their action on the organic pollutants and stability, are analysed. Finally, the challenges of this technology to open up new avenues of wastewater treatment in the future are sketched out.

Soil pollution has become a substantial environmental problem which is amplified by overpopulation in different regions. In this review, the state of the art regarding the use of Advanced Oxidation Processes (AOPs) for soil remediation is presented. This review aims to provide an outline of recent technologies developed for the decontamination of polluted soils by using AOPs. Depending on the decontamination process, these techniques have been presented in three categories: the Fenton process, sulfate radicals process, and coupled processes. The review presents the achievements of, and includes some reflections on, the status of these emerging technologies, the mechanisms, and influential factors. At the present, more investigation and development actions are still desirable to bring them to real full-scale implementation.

The hunt for efficient and environmentally friendly degradation processes has positioned the heterogeneous advanced oxidation processes as an alternative more interesting and economical rather than homogenous processes. Hence, the current study lies in investigating the efficiency of different heterogeneous catalysts using transition metals in order to prevent the generation of iron sludge and to extend the catalogue of possible catalysts to be used in advanced oxidation processes. In this study, nickel and zinc were tested and the ability for radical-generation degradation capacity of both ions as homogeneous was evaluated in the electro-Fenton-like degradation of 2-phenylphenol. In both cases, the degradation profiles followed a first-order kinetic model with the highest degradation rate for nickel (1 mM) with 2-phenylphenol removal level of 90.12% and a total organic reduction near 70% in 2 h. To synthesise the heterogeneous nickel catalyst, this transition metal was fixed on perlite by hydrothermal treatment and in a biochar or carbon nanofibers by adsorption. From the removal results using the three synthesized catalysts, it is concluded that the best catalysts were obtained by inclusion of nickel on biochar or nanofibers achieving in both with removal around 80% before 1 h. Thus, to synthetize a nickel electrocatalyst, nickel doped nanofibers were included on carbon felt. To do this, the amount of carbon black, nickel nanofibers and polytetrafluoroethylene to add on the carbon felt was optimized by Taguchi design. The obtained results revealed that under the optimised conditions, a near-complete removal was achieved after 2 h with high stability of the nickel electrocatalyst that open the applicability of this heterogeneous system to operate in flow systems.

In this study, the removal of persistent emerging and dangerous pollutants (pharmaceuticals and pathogens) in synthetic wastewater was evaluated by the application of heterogeneous Advanced Oxidation Processes. To do that, a Metal-Organic Framework (MOF), Basolite® F-300 was selected as a catalyst and combined with peroxymonosulfate (PMS) as oxidants in order to generate sulphate radicals. Several key parameters such as the PMS and Basolite® F-300 concentration were evaluated and optimized using a Central Composite Experimental Design for response surface methodology for the inactivation of Escherichia coli. The assessment of the degradation of an analgesic and antipyretic pharmaceutical, antipyrine, revealed that is necessary to increase the concentration of PMS and amount of Basolite® F-300, in order to diminish the treatment time. Finally, the PMS-Basolite® F-300 system can be used for at least four cycles without a reduction in its ability to disinfect and degrade persistent emerging and dangerous pollutants such as pharmaceuticals and pathogens.

In this study, three CuFe-MOFs were successfully synthesized by a solvothermal process by changing the ratio of solvents, salts, or temperature. These MOFs named CuFe(BDC-NH2)R, CuFe(BDC-NH2)S, and CuFe(BDC-NH2)D showed rod-shaped, spindle-like, and diamond-like structures, respectively. The CuFe(BDC-NH2)D and CuFe(BDC-NH2)S were found to exhibit an improved PMS activation for Rhodamine B removal attaining levels around 92%. Their effective removal capability was investigated as a function of the pH, catalyst dosage, and the effect of the application of UV radiation. The best degradation system was photo-assisted activation of PMS when CuFe(BDC-NH2)D and CuFe(BDC-NH2)S were used. Under these conditions, the degradation of a mixture of antibiotic and anti-inflammatory drugs (sulfamethoxazole and antipyrine) was evaluated with the results revealing the total degradation of both drugs after 1 h. A higher antibacterial activity was attained with the system CuFe(BDC-NH2)R/PMS due to the high copper content with respect to the others.