In the context of climate change and the circular economy, biochar agricultural and environmental applications have attracted a good deal of attention. Biochar has unique characteristics like surface area, porosity, water-holding capacity, pH, surface charge, and nutrients. This study reviews the biochar production from olive pomace (OP) and olive stone (OS) byproducts, its chemical and physical characterization, and its environmental application. The current review highlights the conditions for biochar production, the effects of pyrolysis temperature, and feedstock type on the physicochemical properties of biochar. High pyrolysis temperature (>500 °C) promotes a high specific surface area, high porosity (especially for OS biochars), and pH as well as the content of ash and fixed carbon, but generates low cation exchange capacity (CEC) and electrical conductivity (EC) and high values of O/C and H/C ratio. OP biochar also presents a high C amount, and ash content, i.e., rich in nutrients and high alkalizing capacity. OP biochar serves as an important source of plant nutrients, especially potassium. After adding both types of biochar, aggregate stability and the amount of water held in soil increase, and bulk density and bioavailability of trace elements decrease. Thus, biochar from olive mill wastes can be a potential plant nutrient reservoir, a good amendment to improve soil properties and long-term carbon sequestration. Results presented in this review can be used to build designer biochars from olive mill wastes to help solve environmental issues (water purification and pollutant remediation) and are suitable for improving soil physical chemistry characteristics and crop growth.

Global water pollution driven by industrial and agricultural expansion has resulted in the widespread occurrence of persistent contaminants, particularly pharmaceuticals and heavy metals, in groundwater systems. Conventional treatment methods often prove inefficient, costly, and environmentally unsustainable, highlighting the need for innovative in situ remediation technologies. Permeable Reactive Barriers (PRBs) have emerged as a promising and energy-efficient solution for the long-term purification of contaminated aquifers. Their efficiency arises from passive operation, relying on natural groundwater flow to promote pollutant removal through adsorption, ion exchange, precipitation, and redox-driven transformations. This review emphasizes the superior performance of materials such as Activated Carbon, Biochar, Zeolites, and Zero-Valent Iron (ZVI) in the immobilization and reduction in pharmaceuticals and metal ions. Key challenges to PRB longevity include permeability loss and reactive media depletion due to mineral precipitation and biofouling. Advances in hybrid PRB configurations, coupled with electrokinetic (EK) and bioreactor systems, and predictive modeling, particularly Artificial Neural Networks (ANNs), offer pathways to enhance performance, optimize design, and ensure sustainable operation. Overall, PRBs represent a scalable and environmentally sound approach to groundwater remediation, with future progress relying on the development of multifunctional, regenerable materials and integrated design strategies.

This study uses waste materials, specifically diatomaceous earth (DE) that is rich in aluminum and silica, as a sustainable source for aluminosilicate precursors in geopolymers to replace conventional cement in mortar applications. While the use of DE shows promising results, it lacks sufficient alumina content, thereby demanding the introduction of alumina powder. However, the effectiveness of this addition is limited, as unreacted alumina particles were observed in the X-ray diffraction and SEM analyses. This could potentially impact various geopolymer properties due to the incomplete achievement of the desired silicon/aluminum (Si/Al) ratio. Achieving the appropriate Si/Al balance remains crucial for geopolymers to realize their potential as environmentally friendly alternatives to Portland cement.

Nitrophenols are persistent organic pollutants that pose serious environmental and health risks due to their toxic and lipophilic nature. Their persistence arises from strong aromatic stability and resistance to biodegradation, while their lipophilicity facilitates bioaccumulation, exacerbating ecological and human health concerns. To address this challenge, this study focuses on the synthesis and characterization of two different types of hybrid multi-core magnetic catalysts: (i) cobalt ferrite (Co-Fe₂O₄), which exhibits ferrimagnetic properties, and (ii) magnetite (Fe₃O₄), which demonstrates close superparamagnetic behavior and is coated with a novel and less hazardous phloroglucinol–glyoxal-derived resin. This approach aims to enhance catalytic efficiency while reducing the environmental impact, offering a sustainable solution for the degradation of nitrophenols in aqueous matrices. Transmission electron microscopy (TEM) images revealed the formation of a multi-core shell structure, with carbon layer sizes of 6.6 ± 0.7 nm for cobalt ferrite and 4.2 ± 0.2 nm for magnetite. The catalysts were designed to enhance the stability and performance in catalytic wet peroxide oxidation (CWPO) processes using sol–gel and solution combustion synthesis methods, respectively. In experiments of single-component degradation, the carbon-coated cobalt ferrite (CoFe@C) catalyst achieved 90% removal of 2-nitrophenol (2-NP) and 96% of 4-nitrophenol (4-NP), while carbon-coated magnetite (Fe₃O₄@C) demonstrated similar efficiency, with 86% removal of 2-NP and 94% of 4-NP. In the multi-component system, CoFe@C exhibited the highest catalytic activity, reaching 96% removal of 2-NP, 99% of 4-NP, and 91% decomposition of H₂O₂. No leaching of iron was detected in the coated catalysts, whereas the uncoated materials exhibited similar and significant leaching (CoFe: 5.66 mg/L, Fe₃O₄: 12 mg/L) in the single- and multi-component system. This study underscores the potential of hybrid magnetic catalysts for sustainable environmental remediation, demonstrating a dual-function mechanism that enhances catalytic activity and structural stability.