Carbon fiber-reinforced polymers are considered a promising composite for many industrial applications including in the automation, renewable energy, and aerospace industries. They exhibit exceptional properties such as a high strength-to-weight ratio and high wear resistance and stiffness, which give them an advantage over other conventional materials such as metals. Various polymers can be used as matrices such as thermosetting, thermoplastic, and elastomers polymers. This comprehensive review focuses on carbon fiber-reinforced thermoplastic polymers due to the advantages of thermoplastic compared to thermosetting and elastomer polymers. These advantages include recyclability, ease of processability, flexibility, and shorter production time. The related properties such as strength, modulus, thermal conductivity, and stability, as well as electrical conductivity, are discussed in depth. Additionally, the modification techniques of the surface of carbon fiber, including the chemical and physical methods, are thoroughly explored. Overall, this review represents and summarizes the future prospective and research developments carried out on carbon fiber-reinforced thermoplastic polymers.

The main objective of this work is to develop a variety of hybrid high-density polyethylene (HDPE) micro- and nanocomposites and to investigate their thermal, mechanical, and morphological characteristics as a function of number of fillers and their contents percentage. In this study, 21 formulations of the composites were prepared using fillers with different sizes including micro fillers such as talc, calcium carbonate (CaCO₃), as well as nano-filler (fumed silica (FS)) though the melt blending technique. The morphological, mechanical, and thermal properties of the composite samples were evaluated. The morphological study revealed negligible filler agglomerates, good matrix–filler interfacial bonding in case of combined both CaCO₃ and FS into the composites. Sequentially, improvements in tensile, flexural and Izod impact strengths as a function of fillers loading in the HDPE matrix have been reported. The maximum enhancement (%) of tensile, flexural and impact strengths were 127%, 86% and 16.6%, respectively, for composites containing 25% CaCO₃ and 1% FS without any inclusion of talc filler; this indicates that the types/nature, size, quantity and dispersion status of fillers are playing a major role in the mechanical properties of the prepared composites more than the number of the used fillers.

One of the most frequent ways to widen the adsorption range of carbon nitride (CN) is to add a well-known photosensitizer into its basic structure. So far, such attachments have been accomplished by using weak van der Waals forces. However, using strong covalent bonding to attach such photosensitizer with CN is yet to be determined. Here, for the first time, we covalently bonded porphyrin (5,10,15,20-tetrakis(4-(2,4-diamino-1,3,5-triazinyl) phenyl)-Porphyrin (TDP)), a renowned photosensitizer, effectively with CN by thermally balanced molecular strategy. A photoreaction system was set up for the deoxygenated conversion of CO₂ to CO under visible light, where cobalt acted as a redox controller to speed up the charge transportation, while CN-TDP worked as a CO₂ activating photocatalyst. The subsequent photocatalyst has a broader absorbance range, a greater specific surface area, and intramolecular organic connections that help to decrease the electron-hole pairs’ recombination rate. Furthermore, the average weight ratio between urea and TDP was well-tuned, resulting in a fantastic CO₂ photoconversion for CN-TDP_7.0 compared to the blank sample. This substantial increase in photocatalytic activity predicts a significant shift in CN’s specific surface area, band gap, chemical composition, and structure, as well as the efficient separation of photogenerated charge carriers from the ground state (HOMO) to the excited state (LUMO), making it a top candidate for CO₂ photoreduction. At the same time, this approach paves the path for the bottom-up fabrication of carbon nitride nanosheets.

In this work, graphite nanoplatelets (GNP) were incorporated into poly (ethylene terephthalate) (PET) matrix to prepare PET-GNP nanocomposites using a melt compounding followed by compression moulding and then quenching process. Both static and dynamic mechanical properties of these quenched materials were characterized as a function of GNP contents using dynamic mechanical thermal analysis (DMTA) and tensile machine, respectively. The results demonstrated that the addition of GNP improved the stiffness of PET significantly. Additionally, the maximum increase in the storage modulus of 72% at 6 wt.% GNP. The incorporation of GNP beyond 6 wt.% into PET decreases the storage moduli, but they remain higher than pure PET. The observed reduction could be due to agglomeration, resulting in poorer dispersion and distribution of higher levels of GNP into the PET matrix. In contrast to the results for moduli, tensile strength and elongations at break reduce with increasing the GNP content. For example, tensile strength reduced from ∼46 MPa (neat PET) to ∼39 MPa (−15%) for the nanocomposites containing 2 wt.% GNP. This reduction is accompanied by a decline in elongation at break from ∼6.3 (neat PET) to ∼3.4 (−46%) for the same nanocomposites. Such reductions are followed by a gradual decrease in upon further addition of GNP. These reductions indicate that increasing GNP loadings, results in brittleness in nanocomposites. In addition, it was found that quenched PET and composite samples were not fully crystallized after processing and therefore (cold) crystallized during the first heating cycle DMTA, as indicated by a rise in storage moduli above the glass transition temperature during the DMTA first heat. Furthermore, mathematical models based on non-linear theories are developed to capture the experimental data. For this, a set of mechanical stress-strain data is used for model parameters’ identification. Another set of data is used for the model validation that demonstrates good agreements with the experimental study.