Microplastics and Co-pollutants in soil and marine environments: Sorption and desorption dynamics in unveiling invisible danger and key to ecotoxicological risk assessment.

Microplastics (MPs) and their co-pollutants pose significant threats to soil and marine environments, necessitating understanding of their colonization processes to combat the plastic pandemic and protect ecosystems. MPs can act as invisible carriers, concentrating and transporting pollutants, leading to a more widespread and potentially toxic impact than the presence of either MPs or the pollutants alone. Analyzing the sorption and desorption dynamics of MPs is crucial for understanding pollutants amplification and predicting the fate and transport of pollutants in soil and marine environments. This review provides an in-depth analysis of the sorption and desorption dynamics of MPs, highlighting the importance of considering these dynamics in ecotoxicological risk assessment of MPs pollution. The review identifies limitations of current frameworks that neglect these interactions and proposes incorporating sorption and desorption data into robust frameworks to improve the ability to predict ecological risks posed by MPs and co-pollutants in soil and marine environments. However, failure to address the interplay between sorption and desorption can result in underestimation of the true impact of MPs and co-pollutants, affecting livelihoods and agro-employments, and exacerbate poverty and community disputes (SDGs 1, 2, 3, 8, 9, and 16). It can also affect food production and security (SDG 2), life below water and life on land (DSGs 14 and 15), cultural practices, and natural heritage (SDG 11.4). Hence, it is necessary to develop new approaches to ecotoxicological risk assessment that consider sorption and desorption processes in the interactions between the components in the framework to address the identified limitations.

A New 3D Mathematical Model for Simulating Nanofluid Flooding in a Porous Medium for Enhanced Oil Recovery.

Two-phase Darcy's law is a well-known mathematical model used in the petrochemical industry. It predicts the fluid flow in reservoirs and can be used to optimize oil production using recent technology. Indeed, various models have been proposed for predicting oil recovery using injected nanofluids (NFs). Among them, numerical modeling is attracting the attention of scientists and engineers owing to its ability to modify the thermophysical properties of NFs such as density, viscosity, and thermal conductivity. Herein, a new model for simulating NF injection into a 3D porous media for enhanced oil recovery (EOR) is investigated. This model has been developed for its ability to predict oil recovery across a wide range of temperatures and volume fractions (VFs). For the first time, the model can examine the changes and effects of thermophysical properties on the EOR process based on empirical correlations depending on two variables, VF and inlet temperature. The governing equations obtained from Darcy's law, mass conservation, concentration, and energy equations were numerically evaluated using a time-dependent finite-element method. The findings indicated that optimizing the temperature and VF could significantly improve the thermophysical properties of the EOR process. We observed that increasing the inlet temperature (353.15 K) and volume fraction (4%) resulted in better oil displacement, improved sweep efficiency, and enhanced mobility of the NF. The oil recovery decreased when the VF (>4%) and temperature exceeded 353.15 K. Remarkably, the optimal VF and inlet temperature for changing the thermophysical properties increased the oil production by 30%.

Recent advances in the biocatalytic mitigation of emerging pollutants: A comprehensive review.

The issue of environmental pollution has been worsened by the emergence of new contaminants whose morphology is yet to be fully understood . Several techniques have been adopted to mitigate the pollution effects of these emerging contaminants, and bioremediation involving plants, microbes, or enzymes has stood out as a cost-effective and eco-friendly approach. Enzyme-mediated bioremediation is a very promising technology as it exhibits better pollutant degradation activity and generates less waste. However, this technology is subject to challenges like temperature, pH, and storage stability, in addition to recycling difficulty as it is arduous to isolate them from the reaction media. To address these challenges, the immobilization of enzymes has been successfully applied to ameliorate the activity, stability, and reusability of enzymes. Although this has significantly increased the uses of enzymes over a wide range of environmental conditions and facilitated the use of smaller bioreactors thereby saving cost, it still comes with additional costs for carriers and immobilization. Additionally, the existing immobilization methods have their individual limitations. This review provides state-of-the-art information to readers focusing on bioremediation using enzymes. Different parameters such as: the sustainability of biocatalysts, the ecotoxicological evaluation of transformation contaminants, and enzyme groups used were reviewed. The efficacy of free and immobilized enzymes, materials and methods for immobilization, bioreactors used, challenges to large-scale implementation, and future research needs were thoroughly discussed.

Preparation and modification methods of defective titanium dioxide-based nanoparticles for photocatalytic wastewater treatment-a comprehensive review.

The rapid population growth and industrial expansion worldwide have created serious water contamination concerns. To curb the pollution issue, it has become imperative to use a versatile material for the treatment. Titanium dioxide (TiO2) has been recognized as the most-studied nanoparticle in various fields of science and engineering due to its availability, low cost, efficiency, and other fascinating properties with a wide range of applications in modern technology. Recent studies revealed the photocatalytic activity of the material for the treatment of industrial effluents to promote environmental sustainability. With the wide band gap energy of 3.2 eV, TiO2 can be activated under UV light; thus, many strategies have been proposed to extend its photoabsorption to the visible light region. In what follows, this has generated increasing attention to study its characteristics and structural modifications in different forms for photocatalytic applications. The present review provides an insight into the understanding of the synthesis methods of TiO2, the current progress in the treatment techniques for the degradation of wide environmental pollutants employing modified TiO2 nanoparticles, and the factors affecting its photocatalytic activities. Further, recent developments in using titania for practical applications, the approach for designing novel nanomaterials, and the prospects and opportunities in this exciting area have been discussed.

Study on Selected Metal-Organic Framework-Based Catalysts for Cycloaddition Reaction of CO2 with Epoxides: A Highly Economic Solution for Carbon Capture and Utilization.

The level of carbon dioxide in the atmosphere is growing rapidly due to fossil fuel combustion processes, heavy oil, coal, oil shelter, and exhausts from automobiles for energy generation, which lead to depletion of the ozone layer and consequently result in global warming. The realization of a carbon-neutral environment is the main focus of science and academic researchers of today. Several processes were employed to minimize carbon dioxide in the air, some of which include the utilization of non-fossil sources of energy like solar, nuclear, and biomass-based fuels. Consequently, these sources were reported to have a relatively high cost of production and maintenance. The applications of both homogeneous and heterogeneous processes in carbon capture and storage were investigated in recent years and the focus now is on the conversion of CO2 into useful chemicals and compounds. It was established that CO2 can undergo cycloaddition reaction with epoxides under the influence of special catalysts to give cyclic carbonates, which can be used as value-added chemicals at a different level of pharmaceutical and industrial applications. Among the various catalysts studied for this reaction, metal-organic frameworks are now on the frontline as a potential catalyst due to their special features and easy synthesis. Several metal-organic framework (MOF)-based catalysts were studied for their application in transforming CO2 to organic carbonates using epoxides. Here, we report some recent studies of porous MOF materials and an in-depth discussion of two repeatedly used metal-organic frameworks as a catalyst in the conversion of CO2 to organic carbonates.

One-pot synthesis of Au@SiO(2) catalysts: a click chemistry approach.

Using the copper-catalyzed azide-alkyne cycloaddition "click" reaction, a library of triazole amphiphiles with a variety of functional polar "heads" and hydrophobic or superhydrophobic "tails" was synthesized. The amphiphiles were evaluated for their ability to stabilize small Au nanoparticles, and, at the same time, serve as templates for nanocasting porous SiO2. One of the Au@SiO2 materials thus prepared was found to be a highly active catalyst for the Au nanoparticle-catalyzed regioselective hydroamination of alkynes.

Porphyrin-naphthodiimide interactions as a structural motif in foldamers and supramolecular assemblies.

pi-pi Stacking interactions between electron deficient naphthalenediimides (NDI) and electron-rich porphyrins (POR) leading to charge transfer are shown to be prevalent in linked NDI-POR and POR-NDI-POR structures. For flexibly-linked systems, intramolecular interactions lead to S-shaped foldamers in solution, whereas intermolecular association is predominant in more rigid systems. The foldamer structures can be interrupted by competing aromatic solvents, by six-coordination of metallated porphyrin derivatives, by protonation of the free base porphyrin in non-metallated structures, and in facially sterically hindered porphyrins.