The current environmental and potable water crisis requires technological advancement to tackle the issues caused by different organic pollutants. Herein, we report the degradation of organic pollutants such as Congo Red and acetophenone from aqueous media using visible light irradiation. To harvest the solar energy for photocatalysis, we fabricated a nanohybrid system composed of bismuth ferrite nanoparticles with two-dimensional (2D) MXene sheets, namely, the BiFeO₃ (BFO)/Ti₃C₂ (MXene) nanohybrid, for enhanced photocatalytic activity. The hybrid BFO/MXene is fabricated using a simple and low-cost double-solvent solvothermal method. The SEM and TEM images showed that the BFO nanoparticles are attached onto the surface of 2D MXene sheets. The photocatalytic degradation achieved by the hybrid is found to be 100% in 42 min for the organic dye (Congo Red) and 100% for the colorless aqueous pollutant (acetophenone) in 150 min. The BFO/MXene hybrid system exhibited a large surface area of 147 m² g^–1 measured via the Brunauer–Emmett–Teller sorption–desorption technique, which is found to be the largest among all BFO nanoparticles and derivatives. The photoluminescence spectra indicate a low electron–hole recombination rate. Fast and efficient degradation of organic molecules is caused by two factors: larger surface area and lower electron–hole recombination rate, which makes the BFO/MXene nanohybrid a highly efficient photocatalyst and a promising candidate for many future applications.

Over the years, scarcity of fresh potable water has increased the demand for clean water. Meanwhile, with the advent of nanotechnology, the use of nanomaterials for photocatalytic degradation of pollutants in wastewaters has increased. Herein, a new type of nanohybrids of La- and Mn-codoped bismuth ferrite (BFO) nanoparticles embedded into transition-metal carbide sheets (MXene–Ti₃C₂) were prepared by a low-cost double-solvent sol–gel method and investigated for their catalytic activity in dark and photoinduced conditions. The photoluminescence results showed that pure BFO has the highest electron hole recombination rate as compared to all the codoped BFO/Ti₃C₂ nanohybrids. The higher electron–hole pair generation rate of the nanohybrids provides a suitable environment for fast degradation of organic dye molecules. The band gap of the prepared nanohybrid was tuned to 1.73 eV. Moreover, the BLFO/Ti₃C₂ and BLFMO-5/Ti₃C₂ degraded 92 and 93% of the organic pollutant, respectively, from water in dark and remaining in the light spectrum. Therefore, these synthesized nanohybrids could be a promising candidate for catalytic and photocatalytic applications in future.

This article details a comparison of the photocatalytic activity of La, Mn co-doped BiFeO₃/GNP nanohybrids prepared by co-precipitation and hydrothermal methods.

This work aims to provide an extensive evaluation on the use of polylactic acid (PLA) as a green, biodegradable thermal insulation material. The PLA was processed by melt extrusion followed by compression molding and then subjected to different annealing conditions. Afterwards, the thermal insulation properties and structural capacity of the PLA were characterized. Increasing the annealing time of PLA in the range of 0–24 h led to a considerable increase in the degree of crystallization, which had a direct impact on the thermal conductivity, density, and glass transition temperature. The thermal conductivity of PLA increased from 0.0643 $\mathrm{W}/\left(\mathrm{m}·\mathrm{K}\right)$ for quickly-cooled samples to 0.0904 $\mathrm{W}/\left(\mathrm{m}·\mathrm{K}\right)$ for the samples annealed for 24 h, while the glass transition temperature increased by approximately 11.33% to reach 59.0 °C. Moreover, the annealing process substantially improved the compressive strength and rigidity of the PLA and reduced its ductility. The results revealed that annealing PLA for 1–3 h at 90 °C produces an optimum thermal insulation material. The low thermal conductivity (0.0798–0.0865 $\mathrm{W}/\left(\mathrm{m}·\mathrm{K}\right)$), low density (~1233 $\mathrm{kg}/{\mathrm{m}}^3$), very low water retention (<0.19%) and high compressive strength (97.2–98.7 MPa) in this annealing time range are very promising to introduce PLA as a green insulation material.

In this study, silica in the form of raw local natural sand was added to high-density-polyethylene (HDPE) in order to develop a composite material in the form of sheets that could have potential applications in thin film industries, such as packaging, or recycling industries, such as in 3D printing. The silica/HDPE composite sheets were developed using a melt extruder followed by using a hot press for compression molding. The impact of two different particle sizes (25 µm and 5 µm) of the silica particles on selected properties such as toughness, elastic modulus, ductility, and composite density were analyzed. A considerable increase in the toughness and elastic modulus was observed from 0 wt% to 20 wt% with a 25 µm filler size. However, a general decreasing trend was observed in the material’s toughness and elastic modulus with decreasing particle size. A similar trend was observed for the ductility and the tensile strength of the sheets prepared from both filler particle sizes. In terms of the composite density, as the filler was increased from 20 wt% to 50 wt%, an increase in the composite densities was noticed for both particle sizes. Additionally, the sheets developed with 25 µm particle size had a slightly higher density than the 5 µm particle size, which is expected as the size can account for the higher weight. Results from this work aim to analyze the use of local sand as a filler material that can contribute towards maximizing the potential of such composite materials developed in extrusion industries.