Glass-fiber-reinforced polymer (GFRP) composites are widely used due to their high strength-to-weight ratio and corrosion resistance. However, their properties can degrade under different environmental conditions, affecting long-term reliability. This study examines the effects of temperature and chemical environments on GFRP pipes. Specimens were exposed to salt water and alkaline solutions at 20 °C and 50 °C. Diffusion coefficients and tensile and flexural properties were measured. Advanced techniques (TGA, FT-IR, and XRD) showed a 54.73% crystallinity difference between samples at 20 °C/air and 50 °C/salt water. Elevated temperatures and alkaline conditions accelerated degradation, with diffusion coefficients 68.38% higher at 50 °C/salt water compared to at 20 °C/salt water. Flexural strength decreased by 47.65% and tensile strength by 13.89%, at 50 °C/alkaline compared to 20 °C/air. Temperature was identified as the primary factor affecting mechanical performance, while alkaline environments significantly influenced tensile and flexural modulus. These results underscore the importance of considering environmental factors for the durability of GFRP composites.

The removal yield of organic substances present in water depends on the environmental conditions, on the chemical composition of the water and on the chemical substance dissolved in the water, which constitutes the substrate of the metabolic activities of the microalgae that use these substances in the biochemical reactions of cellular enzyme complexes. o-Chlorobenzylidene malononitrile (CS, to use its military designation) was synthesized in-house, for research purposes, by a condensing reaction between o-chlorobenzaldehide and malononitrilein the presence of diethylamine. The detection, identification and confirmation of o-chlorobenzylidenemalononitrile (coded CBM in this experimental study) was performed using gas chromatography–mass spectrometry (GC-MS) and the purity of CBM was 99%. The biodegradation capacity in the samples that contained the biological suspension, after 24 h and 96 h of incubation, was determined via GC-MS analysis, and no evidence of the presence of CBM or some metabolites of CBM was detected. In the parallel samples, a hydrolysis process of CBM at room temperature, without biological treatment, revealed two main metabolites, malononitrile and o-chlorobenzaldehyde, respectively. This study is focused on evaluating the biodegradation capacity of o-chlorobenzylidene malononitrile in the presence of a biological material, culture of Chlorella sp., in comparison with a classical hydrolysis process. The tests performed indicate that the suspension of Chlorella sp. consumed the entire amount of CBM and metabolites from the analyzed samples. The tests prove that the biological material can be used to decontaminate the affected areas.

Fiber-reinforced polymers (FRPs) are increasingly recognized in sustainable materials research due to their potential environmental advantages. This study presents a focused bibliometric review of the sustainability research on FRPs. An initial search of the Web of Science (WOS) database identified 803 documents, which were refined to 749 relevant articles, reviews, and proceedings. A co-authorship analysis highlights the significant contributions of the USA and India, with European countries forming regional collaborations. The research output has steadily increased since 2011, peaking in 2022 and 2023. The multidisciplinary nature of the research spans materials science, engineering, and environmental sciences, with journals such as *Polymers*, *Sustainability*, and the *Journal of Cleaner Production* emphasizing sustainability themes. This analysis covers key aspects such as keyword co-occurrence, overlay visualizations, co-authorship networks, and the distribution of publications by year, research area, and journal. The findings underscore the evolving research landscape of sustainable FRPs and highlight the ongoing need for life cycle assessments and interdisciplinary collaboration.

This study investigates chlorine-induced aging of high-density polyethylene (HDPE) through a 3 × 3 factorial matrix combining three temperatures (20, 40, 60 °C) and three chlorine concentrations (5, 10, 20 ppm) over 45 days. Tensile tests revealed progressive embrittlement, with elongation at break decreasing sharply under severe aging; samples exposed to 60 °C and 20 ppm exhibited premature brittle failure despite peak stresses remaining near ~22 MPa. XRD results showed a reduction in crystallinity from 67.07% (reference) to 61.06–61.31% under the most aggressive conditions, accompanied by a decrease in crystallite size from 5.60 nm to 2.10–2.50 nm. FTIR analysis confirmed oxidation through increased carbonyl absorption at 1716 cm⁻¹ and new bands at 1608–1635 cm⁻¹. TGA revealed substantial thermal deterioration, with T5% falling from 450 °C (reference) to 327 °C at 60 °C/20 ppm, along with an additional degradation peak at 398 °C. DSC showed a melting temperature decrease from 136.32 °C to 131.67 °C and an increase in crystallinity from 41.07% (unexposed sample) to 59.19% (60 °C/20 ppm). Statistical analysis of the results established that degradation is governed by different dominant factors depending on the measured property: Chlorine concentration was found to be the dominant factor for XRD crystallinity and thermal decomposition T5%, confirming that surface structural damage and early molecular weight loss are driven primarily by chlorine-induced oxidation. Conversely, DSC crystallinity was governed primarily by temperature, reflecting thermally driven molecular reorganization within the bulk material. Overall, chlorine exposure, amplified by temperature, accelerates chemical oxidation, structural degradation, and mechanical embrittlement, reducing the long-term reliability of HDPE in chlorinated water systems. The findings provide critical data for predicting the service life and informing material selection for HDPE components used in high-temperature or high-chlorine water distribution systems.

This study investigates the wear behavior and multi-technique characterization of 3D printed thermoplastic polyurethane (TPU) intended for friction layers in transmission belts used in pharmaceutical manipulators. Two flexible TPU grades—TPU 51A and TPU 60A—were printed using fused deposition modeling (FDM) with varying printing temperatures (255–265 °C for 51A; 225–235 °C for 60A) and layer counts (three or four layers). Specimens were evaluated for Shore A hardness, wear resistance (mass loss using a Baroid lubricity tester under dry sliding against carton), tensile properties, crystallinity (XRD), chemical structure (FTIR), thermal stability (TGA), and scanning electron microscopy (SEM). The results show that printing parameters significantly influence the mechanical and tribological behavior of the materials. For TPU 51A, increasing the printing temperature to 265 °C and using four layers led to a substantial reduction in cumulative mass loss, although hardness decreased. In contrast, for TPU 60A, higher printing temperature and layer count increased hardness but also resulted in higher wear. Tensile tests indicated that specimens printed with fewer layers exhibited higher yield strength and strain, indicating improved interlayer bonding. XRD analysis confirmed the predominantly amorphous nature of the printed samples, with a reduction in crystallinity compared to the raw filaments. FTIR spectra showed no significant chemical degradation during printing, while thermogravimetric analysis revealed good thermal stability up to approximately 250–260 °C. The results demonstrate that wear behavior is governed by a combination of hardness, interlayer cohesion, and microstructural organization rather than crystallinity alone. Among the investigated conditions, TPU 51A printed at 265 °C with four layers exhibited the most favorable balance between wear resistance and mechanical properties, highlighting its suitability for friction layer applications.

Bio-oil is the liquid fraction obtained from the pyrolysis process and is an important source of