In recent decades, the rising wastewater output from industrial pollution has inflicted severe harm on both surface and groundwater, leading to substantial environmental damage. The elimination of harmful, toxic materials and wastewater remediation are pressing global concerns and pose a formidable challenge for scientists worldwide. Heterogeneous photocatalysis has been recognized as a promising, effective, energy-free, and eco-friendly process capable of completely degrading various organic pollutants. Finding a material that simultaneously satisfies various thermodynamic and kinetic criteria, coupled with good thermal- and photo-stability, is a challenging task necessitating the modification of existing materials or the synthesis of new ones to meet the required standards. This present study comprehensibly elaborates on different approaches to the modification of various photocatalytic systems, both organic and inorganic, in order to obtain more efficient and feasible catalysts for practical applications. In addition, the current status of the application of photocatalysts in dye wastewater treatment is summarized, projecting the future direction for wastewater management by photocatalytic processes.

Layered double hydroxides (LDHs) have been studied to a great extent as environmental-friendly complex materials that can be used as photocatalysts or photocatalyst supports. ZnAl layered double hydroxides and their derived mixed oxides were chosen for the investigation of photocatalytic performances in correlation with the UV intensities measured in the South Pannonia region. Low supersaturation coprecipitation method was used for the ZnAl LDH synthesis. For the characterization of LDH and thermal treated samples powder X-ray diffraction (XRD), scanning electron microscopy (SEM), electron dispersive spectroscopy (EDS), nitrogen adsorption-desorption were used. The decomposition of azodye, methylene blue was chosen as photocatalytic test reaction. The study showed that the ZnAl mixed oxide obtained by thermal decomposition of ZnAl LDH has stable activity in the broader UV light irradiation range characterizing the selected region. Photocatalytic activity could be mainly attributed to the ZnO phase, detected both in LDH and thermally treated samples. The study showed that the ZnAl mixed oxide obtained by the calcination of ZnAl LDH has a stable activity within the measured UV light irradiation range; whereas the parent ZnAl LDH catalyst did not perform satisfactory when low UV irradiation intensity is implied.

Layered double hydroxides (LDHs) have gained increasing attention as versatile materials in environmental remediation, particularly for wastewater treatment. Their unique structural properties, such as tunable metal cation composition, interlayer anion exchange, and structural memory effects, make them suitable materials for a broad range of applications. In addition to these intrinsic properties, thermally treated LDH-derived mixed metal oxides have emerged as a key focus, exhibiting enhanced activity through tailored structural, electronic, and textural properties. This review presents an up-to-date and systematic overview of recent advancements in the design and application of LDH-based materials, with a focus on photocatalytic degradation of organic dyes, adsorption of contaminants, and light-activated antimicrobial activity. The review also explores emerging photocatalytic applications in correlation with surface engineering, heterojunction formation, and thermal activation to enhance the overall efficiency. In addition, the synergy between antimicrobial activity and photocatalysis is discussed in the context of achieving multifunctional microbial control in water treatment. Finally, current challenges and future perspectives are addressed, including recyclability, scale-up potential, and the development of LDH composites as sustainable alternatives to conventional photocatalysts. This review aims to support researchers in advancing LDH-based technologies toward more efficient and versatile environmental remediation solutions.

Waste and recycled materials have recently been used in the construction industry to comply with the principles of circular economy and sustainable development. The aim of this paper is to examine the potentials of solidified wastewater treatment sludge (SWWTS) as a supplementary cementitious material (SCM) in the production of lightweight pervious concrete pavers (LWPCP) suitable for pedestrian trails and rooftops (green) that comply with EU standards. Detailed characterization of SWWTS was performed, in order to understand its properties related to application as SCM, which led to the conclusion that it may be applied only as a filler, having 89.5% of Ca(OH)₂. After thorough characterization, LWPCP samples were prepared and testing of physical and mechanical properties was conducted. The research showed that partial replacement of cement with SWWTS led to the decrease of all mechanical properties, ranging between 3.91 and 5.81 MPa for compressive strength and 0.97 to 1.23 MPa for flexural strength. However, all of the investigated mixtures showed a value higher than 3.5 MPa, which was defined as the lowest compressive strength in the range of pervious concrete properties. The addition of SWWTS led to a slight decrease in bulk density of the mixtures and an increase in water absorption. This could be explained by the reduction in hydration products that would fill in the micropores of the matrix, since SWWTS showed no pozzolanic reactivity. Pore sizes that prevail in the tested binder matrices are in accordance with the results measured on ordinary pervious concrete (the largest fraction of pores had a diameter between 0.02 and 0.2 μm). Low thermal conductivity nominates produced pavers as potential rooftop elements.

The influence of surface properties on the selectivity of the synthesized catalysts was studied, considering that their selectivity towards particular hydrocarbons is crucial for their overall activity in the chosen Fischer- -Tropsch reaction. Magnesium- and iron-containing layered double hydroxides (LDH), with the general formula: [Mg1-xFex(OH)2](CO3)x/2?mH2O, x = = n(Fe)/(n(Mg)+n(Fe)), synthesized with different Mg/Fe ratio and their thermally derived mixed oxides were investigated. Magnesium was chosen because of its basic properties, whereas iron was selected due to its well-known high Fischer-Tropsch activity, redox properties and the ability to form specific active sites in the layered LDH structure required for catalytic application. The thermally less stable multiphase system (synthesized outside the optimal single LDH phase range with additional Fe-phase), having a lower content of surface acid and base active sites, a lower surface area and smaller fraction of smaller mesopores, showed higher selectivity in the Fischer-Tropsch reaction. The results of this study imply that the metastability of derived multiphase oxides structure has a greater influence on the formation of specific catalyst surface sites than other investigated surface properties.