Pyrolysis of polypropylene (PP) and high density polyethylene (HDPE) into fuel like products was investigated over temperature range of 250– 400°C. The product yields as a function of temperature were studied. Total conversion as high as 98.66% (liquid; 69.82%, gas; 28.84%, and residue; 1.34%) was achieved at 300°C in case of PP and 98.12% (liquid; 80.88%, gas; 17.24%, and residue; 1.88%) in case of HDPE at 350°C. The liquid fractions were analyzed by FTIR and GC-MS. The results showed that the liquid fractions consisted of a wide range of hydrocarbons mainly distributed within the C₆–C₁₆. The liquid product obtained in case of PP is enriched in the naphtha range hydrocarbons. Similarly, the liquid product obtained in case of HDPE is also enriched in naphtha range hydrocarbons with preponderance in gasoline and diesel range hydrocarbons. The% distribution of paraffinic, olefinic, and naphthenic hydrocarbons in liquid product derived from PP is 66.55, 25.7, and 7.58%, respectively, whereas in case HDPE, the% distribution is 59.70, 31.90, and 8.40%, respectively. Upon comparing the hydrocarbon group type yields, PP gave high yield of paraffinic hydrocarbons while HDPE gave high yields of olefins and naphthenes. The whole liquid fractions and their corresponding distillates fractions were also analyzed for fuel properties. The results indicated that the derived liquid fractions were fuel-like meeting the fuel grade criteria.

In this study, oxidative desulfurization (ODS) of modeled and real oil samples was investigated using manganese-dioxide-supported, magnetic-reduced graphene oxide nanocomposite (MnO₂/MrGO) as a catalyst in the presence of an H₂O₂/HCOOH oxidation system. MnO₂/MrGO composite was synthesized and characterized by scanning electron microscope (SEM), energy dispersive X-ray spectroscopy (EDX), Fourier transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD) analyses. The optimal conditions for maximum removal of dibenzothiophene (DBT) from modeled oil samples were found to be efficient at 40 °C temperature, 60 min reaction time, 0.08 g catalyst dose/10 mL, and 2 mL of H₂O₂/formic acid, under which MnO₂/MrGO exhibited intense desulfurization activity of up to 80%. Under the same set of conditions, the removal of only 41% DBT was observed in the presence of graphene oxide (GO) as the catalyst, which clearly indicated the advantage of MrGO in the composite catalyst. Under optimized conditions, sulfur removal in real oil samples, including diesel oil, gasoline, and kerosene, was found to be 67.8%, 59.5%, and 51.9%, respectively. The present approach is credited to cost-effectiveness, environmental benignity, and ease of preparation, envisioning great prospects for desulfurization of fuel oils on a commercial level.

Polymer composites are favorite materials for sensing applications due to their low cost and easy fabrication. In the current study, composite nanofibers consisting of polyethylene oxide (PEO), oxidized multi-walled carbon nanotubes (MWCNT) and copper oxide (CuO) nanoparticles with 1% and 3% of fillers (i.e., PEO–CuO–MWCNT: 1%, and PEO–CuO–MWCNT: 3%) were successfully developed through electrospinning for humidity sensing applications. The composite nanofibers were characterized by FTIR, XRD, SEM and EDX analysis. Firstly, they were loaded on an interdigitated electrode (IDE), and then the humidity sensing efficiency was investigated through a digital LCR meter (E4980) at different frequencies (100 Hz–1 MHz), as well as the percentage of relative humidity (RH). The results indicated that the composite nanofibers containing 1% and 3% MWCNT, combined with CuO in PEO polymer matrix, showed potent resistive and capacitive response along with high sensitivity to humidity at room temperature in an RH range of 30–90%. More specifically, the PEO–CuO–MWCNT: 1% nanocomposite displayed a resistive rapid response time within 3 s and a long recovery time of 22 s, while the PEO–CuO–MWCNT: 3% one exhibited 20 s and 11 s between the same RH range, respectively.

The current study reports the effect of different wt. ratios of copper oxide nanoparticle (CuO-NPs) and reduced graphene oxide (rGO) as fillers on mechanical, electrical, and thermal properties of waste polystyrene (WPS) matrix. Firstly, thin sheets of WPS-rGO-CuO composites were prepared through solution casting method with different ratios, i.e., 2, 8, 10, 15 and 20 wt.% of CuO-NPs and rGO in WPS matrix. The synthesized composite sheets were characterized by Fourier transform infrared spectroscopy (FTIR), energy dispersive X-ray (EDX), X-ray diffraction (XRD) analysis, scanning electron microscopy (SEM) and thermal gravimetric analysis (TGA). The electrical conductance and mechanical strength of the prepared composites were determined by using LCR meter and universal testing machine (UTM). These properties were dependent on the concentrations of CuO-NPs and rGO. Results display that the addition of both fillers, i.e., rGO and CuO-NPs, collectively led to remarkable increase in the mechanical properties of the composite. The incorporation of rGO-CuO: 15% WPS sample, i.e., WPS-rGO-CuO: 15%, has shown high mechanical strength with tensile strength of 25.282 MPa and Young modulus of 1951.0 MPa, respectively. Similarly, the electrical conductance of the same composite is also enhanced from 6.7 × 10⁻¹⁴ to 4 × 10⁻⁷ S/m in contrast to WPS at 2.0 $\times$ 10⁶ Hz. The fabricated composites exhibited high thermal stability through TGA analysis in terms of 3.52% and 6.055% wt. loss at 250 °C as compared to WPS.