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Ultrasound imaging is a widely used technique in every health care center and hospital. Ultrasound gel is used as a coupling medium in all ultrasound procedures to replace air between the transducer and the patient’s skin, as ultrasound waves have trouble in traveling through air. This research was performed to formulate an inexpensive alternative to commercially available ultrasound gel as it is expensive and imported from other countries. Different formulations with different concentrations of carbopol 980 (CAR 980) and methylparaben were prepared with natural ingredients such as aloe vera gel and certain available chemicals that have no harmful effects on the skin. To justify the efficiency of the formulations; necessary physicochemical characteristics such as visual clarity, homogeneity, transparency, skin irritation, antibacterial activity, pH, stability, spreadability, conductivity, acoustic impedance, viscosity, and cost were evaluated. Moreover, a comparison study was also conducted with commercially available ultrasound gel that was utilized as a control. All samples showed excellent transparency and no microbial growth. S1 was the only formulation that met all of the requirements for commercial ultrasound gel and produced images that were similar to those produced by commercial ultrasound gel. So, this formulation could be used as an alternative to expensive commercial ultrasound gel for taking images in hospitals and medical centers.

The co-precipitation and in situ modified Hummers’ method was used to synthesize Nickel Spinal Ferrites (NiFe) nanoparticles and NiFe coated with Thermally Reduced Graphene Oxide (TRGO) (NiFe-TRGO) nanoparticles, respectively. By using polyvinyl chloride (PVC), tetrahydrofuran (THF), and NiFe-TRGO, the nanocomposite film was synthesized using the solution casting technique with a thickness of 0.12–0.13 mm. Improved electromagnetic interference shielding efficiency was obtained in the 0.1–20 GHz frequency range. The initial assessment was done through XRD for the confirmation of the successful fabrication of nanoparticles and DC conductivity. The microstructure was analyzed with scanning electron microscopy. The EMI shielding was observed by incorporating a filler amount varying from 5 wt.% to 40 wt.% in three different frequency regions: microwave region (0.1 to 20 GHz), near-infrared (NIR) (700–2500 nm), and ultraviolet (UV) (200–400 nm). A maximum attenuation of 65 dB was observed with a 40% concentration of NiFe-TRGO in nanocomposite film.

In this study, cellulose acetate (CA) was blended with sulfonated graphene oxide (SGO) nanomaterials to endow a nanocomposite membrane for wastewater treatment with improved hydrophilicity and anti-biofouling behavior. The phase inversion method was employed for membrane fabrication using tetrahydrofuran (THF) as the solvent. The characteristics of CA-SGO-doped membranes were investigated through thermal analysis, contact angle, SEM, FTIR, and anti-biofouling property. Results indicated that anti-biofouling property and hydrophilicity of CA-SGO nanocomposite membranes were enhanced with addition of hydrophilic SGO nanomaterials in comparison to pristine CA membrane. FTIR analysis confirmed the successful decoration of SGO groups on CA membrane surface while revealing its morphological properties through SEM analysis. Thermal analysis performed using DSC confirmed the increase in thermal stability of CA-SGO membranes with addition of SGO content than pure CA membrane.

Sustainable packaging solutions are of paramount importance in addressing the environmental challenges posed by conventional non-biodegradable materials. This study addresses this critical need by introducing a novel approach to crafting antimicrobial biodegradable polymer films. Leveraging the benefits of polyvinyl alcohol (PVA) as a base material, combined with corn-starch (CS) and mint extract (ME), these films offer a compelling synergy of eco-friendliness, antimicrobial efficacy, and mechanical strength. The antimicrobial property was imparted by adding mint extract, and boric acid (BA) was added as a cross-linker for better mechanical properties. All process was done by solution casting method followed by mechanical stirring. After 7 days, starch-PVA blend showed 50% weight loss; however, after adding mint extract, the action of microbes was reduced, and a 50% reduction in weight was observed after 12 days. The excellent mechanical properties were achieved by adding 10% aqueous solution of BA as a cross-linker. The confirmation of BA in the blend was done by the Fourier transform infrared spectroscopy (FTIR). Differential scanning calorimetry (DSC) was used to check the thermal properties of the films. Antimicrobial results showed that mint extract was resistant to staphylococcus aureus bacteria. These biodegradable films offer a multifaceted solution, aligning with sustainability objectives, showcasing antimicrobial potential, and demonstrating mechanical robustness. As such, they hold promise for a diverse array of applications, particularly in the realm of environmentally conscious food packaging. In the pursuit of greener alternatives, these films stand as a testament to innovative materials engineering that harmonizes functionality with ecological responsibility.

This study focuses on developing and characterizing multifunctional composites based on the diglycidyl ether of bisphenol-A (DGEBA) epoxy matrix. The aim is to enhance fire resistance and electrical conductivity properties for applications in various fields. To achieve this, aluminum tri-hydroxide (ATH) was incorporated as a flame retardant (FR) agent, while polyaniline (PANI) was added to impart electrical conductivity. The composites were categorized into three groups: the first containing flame retardant (FR), the second containing PANI for conductivity, and the third containing both PANI and FR for combined effects. E 60-FP emerged as the optimal multifunctional composite, exhibiting superior mechanical properties among the tested formulations. Thermogravimetric analysis (TGA) results provided valuable insights into the thermal stability of E 60-FP, revealing that it retained 42% of its initial mass at a temperature of 600 °C. Additionally, the composite achieved a V-0 rating in the UL 94 test, confirming its excellent fire resistance. Notably, E 60-FP displayed impressive mechanical strength, with a tensile strength of 7.2 MPa and a tensile modulus of 1117.6 MPa. Its flexural strength and modulus were measured at 31.2 MPa and 2800.2 MPa, respectively. Furthermore, the composite E 60-FP exhibited remarkable electrical conductivity, measuring 6.1 × 10 ^–6 S cm ^−1 . These findings highlight the potential of DGEBA epoxy composites containing PANI and ATH as promising materials for applications requiring fire resistance and electrical conductivity properties.