In this study, we successfully address a significant research and engineering gap by quantitatively assessing the impact of varying compressive loading rates on the mechanical behavior of four popular thermoplastic polymers in material-extrusion-based (MEX) 3D printing. Raw powders of polycarbonate (PC), polyethylene terephthalate glycol (PETG), polymethyl methacrylate (PMMA), and thermoplastic polyurethane (TPU) were processed through melt extrusion, and the filaments were used to 3D-print the test samples. For completeness, thermogravimetric analysis and a compressive test following the ASTM-D695 standard were conducted. Ultimately, the compressive strength and yield stress, the compressive modulus of elasticity and toughness, and the maximum compressive sensitivity index were thoroughly documented. Specimens were tested in strain rates from 1.3 mm/min to 200 mm/min. The compressive strength (40% for the PMMA) and stiffness (29% for the TPU) increased with the increase in the strain rate in all polymers tested. PC had the highest strain rate sensitivity. Significant variations in deformation and fracture modes were observed and thoroughly documented throughout this study. Our findings can be useful in industrial engineering as valued design optimization input parameters in various applications involving the above-mentioned polymeric materials.

Both energy efficiency and robustness are popular demands for 3D-printed components nowadays. These opposing factors require compromises. This study examines the effects of seven general control variables on the energy demands and the compressive responses of polyamide (PA6) material extrusion (MEX) 3D printed samples. Nozzle Temperature, Layer Thickness, Orientation Angle, Raster Deposition Angle, Printing Speed, Bed Temperature, and Infill Density were studied. An L27 orthogonal array was compiled with five replicas. A total of 135 trials were conducted, following the ASTM D695-02a specifications. The stopwatch method was used to assess the construction time and energy usage. The compressive strength, toughness, and elasticity modulus were experimentally determined. The Taguchi technique ranks each control parameter’s impact on each response measure. The control parameter that had the greatest impact on both energy use and printing time was layer thickness. Additionally, the infill density had the greatest influence on the compressive strength. Quadratic regression model equations were formed for each of the response measures. The ideal compromise between mechanical strength and energy efficiency is now reported, with merit related to technological and economic benefits.

Glass was introduced as an additive to filaments used for the manufacturing of composite materials, employed by Additive Manufacturing applications. Glass accounts for a large waste electric and electronic equipment (WEEE) percentage, and its recovery and recycling can lead to the production of sustainable composite materials. In this work, poly(lactic acid) (PLA)/commercially available silicon oxide composite filaments were manufactured and their structural, thermal, rheological, and mechanical properties were assessed. Scanning Electron Microscopy confirmed the 1:2 ratio of silicon: oxygen, along with the relatively low adhesion between the filler and the matrix. Differential Scanning Calorimetry presented steady glass transition and melting temperatures of composites, whereas a crystallization temperature of 10% wt. and a crystallinity of 15% wt. composite slightly increased. Rheological analysis showcased that the viscosity of the composite filaments decreased compared to PLA (10–100 compared to 300–400 Pa·s), with a more shear-thinning behavior. Dynamic mechanical analysis exhibited increased elastic, flexural moduli, and flexural strength of composites (up to 16, 23, and 11%, respectively), whereas tensile strength and elongation decreased. The affordability of raw materials (with the future introduction of recycled ones) and the minimal processing steps can lead to the potential scaling up of the study.

In this study, poly (ethylene terephthalate) (PETG) was combined with Antimony-doped Tin Oxide (ATO) to create five different composites (2.0–10.0 wt.% ATO). The PETG/ATO filaments were extruded and supplied to a material extrusion (MEX) 3D printer to fabricate the specimens following international standards. Various tests were conducted on thermal, rheological, mechanical, and morphological properties. The mechanical performance of the prepared nanocomposites was evaluated using flexural, tensile, microhardness, and Charpy impact tests. The dielectric and electrical properties of the prepared composites were evaluated over a broad frequency range. The dimensional accuracy and porosity of the 3D printed structure were assessed using micro-computed tomography. Other investigations include scanning electron microscopy and energy-dispersive X-ray spectroscopy, which were performed to investigate the structures and morphologies of the samples. The PETG/6.0 wt.% ATO composite presented the highest mechanical performance (21% increase over the pure polymer in tensile strength). The results show the potential of such nanocomposites when enhanced mechanical performance is required in MEX 3D printing applications, in which PETG is the most commonly used polymer.

Polyethylene terephthalate glycol (PETG) and silicon nitride (Si₃N₄) were combined to create five composite materials with Si₃N₄ loadings ranging from 2.0 wt.% to 10.0 wt.%. The goal was to improve the mechanical properties of PETG in material extrusion (MEX) additive manufacturing (AM) and assess the effectiveness of Si₃N₄ as a reinforcing agent for this particular polymer. The process began with the production of filaments, which were subsequently fed into a 3D printer to create various specimens. The specimens were manufactured according to international standards to ensure their suitability for various tests. The thermal, rheological, mechanical, electrical, and morphological properties of the prepared samples were evaluated. The mechanical performance investigations performed included tensile, flexural, Charpy impact, and microhardness tests. Scanning electron microscopy and energy-dispersive X-ray spectroscopy mapping were performed to investigate the structures and morphologies of the samples, respectively. Among all the composites tested, the PETG/6.0 wt.% Si₃N₄ showed the greatest improvement in mechanical properties (with a 24.5% increase in tensile strength compared to unfilled PETG polymer), indicating its potential for use in MEX 3D printing when enhanced mechanical performance is required from the PETG polymer.

CDs/TiO₂ nanohybrids were synthesized and tested for photocatalytic H₂ production from aqueous media through simulated solar light-driven photocatalytic reactions. Firstly, three different types of CDs were prepared through green methods, specifically hydrothermal treatment and microwave irradiation, using citric acid and urea as precursors in varying molar ratios. After a multi-step purification procedure, impurity-free CDs were obtained. The as-synthesized CDs were thoroughly characterized using UV-Vis, FT-IR, and PL spectroscopy, along with HR-TEM. The results revealed that the size and optical and physicochemical properties of CDs can be tailored by selecting the precursors’ ratio and the synthetic approach. The heterostructured CDs/TiO₂ photocatalysts were formed solvothermally and were analyzed using UV-Vis/DRS, FT-IR, and XPS techniques, which confirmed the effective incorporation of CDs and the improved properties of TiO₂. The use of sacrificial reagents is among the most common strategies for enhancing H₂ production from water through photocatalytic processes; herein, ethanol was selected as a green liquid organic hydrogen carrier. A maximum H₂ production rate of 0.906 μmol H₂/min was achieved, while the recyclability study demonstrated that the photocatalyst maintained stable performance during multiple cycles of reuse. Thus, optimizing the synthesis conditions of CDs/TiO₂ nanohybrids resulted in the creation of environmentally friendly and reusable photocatalysts.