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Although the supramolecular structure of porphyrin polymers on flat surfaces (i.e., mica and HOPG) has been extensively studied, the self-assembly arrays of porphyrin polymers on the SWNT (as curved nanocarbon surfaces) have yet to be fully identified and/or investigated, especially using microscopic imaging techniques, i.e., scanning tunneling microscopy (STM), atomic force microscopy (AFM), and transmission electron microscopy (TEM). This study reports the identification of the supramolecular structure of poly-[5,15-bis-(3,5-isopentoxyphenyl)-10,20-bis ethynylporphyrinato]-zinc (II) on the SWNT surface using mainly AFM and HR-TEM microscopic imaging techniques. After synthesizing around >900 mer of porphyrin polymer (via Glaser-Hay coupling); the as-prepared porphyrin polymer is then non-covalently adsorbed on SWNT surface. Afterward, the resultant porphyrin/SWNT nanocomposite is then anchored with gold nanoparticles (AuNPs), which are used as a marker, via coordination bonding to produce a porphyrin polymer/AuNPs/SWNT hybrid. The polymer, AuNPs, nanocomposite, and/or nanohybrid are characterized using 1H-NMR, mass spectrometry, UV-visible spectroscopy, AFM, as well as HR-TEM measuring techniques. The self-assembly arrays of porphyrin polymers moieties (marked with AuNPs) prefer to form a coplanar well-ordered, regular, repeated array (rather than wrapping) between neighboring molecules along the polymer chain on the tube surface. This will help with further understanding, designing, and fabricating novel supramolecular architectonics of porphyrin/SWNT-based devices.

This study presents the synthesis and doping of reduced graphene oxide (rGO) with synthesized porphyrin (5,15-bisdodecyl porphyrin, C12P) nanoparticles to fabricate reduced graphene oxide-porphyrin (rGO-P) nanocomposite as well as demonstrates their outstanding removal activity of azo dye and antimicrobial potential. The synthesized porphyrin, rGO, and rGO-P nanocomposites were characterised using SEM, HRTEM, Raman spectroscopy, XRD, 1 H-NMR, mass spectrometry, and UV–Visible spectroscopy. The ability of the synthesized rGO-P nanocomposite was then investigated (as catalyst and/or adsorbent) to impact its removal efficacy against Congo red (CR) as a well-known toxic, mutagenic and carcinogenic synthetic dye. The findings indicated that 0.01 g of rGO-P nanocomposite achieved 78.0% removal of CR at pH 3.0. Besides, the removal efficacy was evaluated while studying many aspects i.e. pH, CR initial concentration, and rGO-P nanocomposite amount. Moreover, the minimum inhibitory concentration (MIC) and zone of inhibition (ZOI) of antimicrobial activity against pathogenic bacteria and yeast were evaluated. The antimicrobial results showed that rGO-P nanocomposite revealed the greatest antimicrobial activity against Candida albicans, Enterococcus faecalis, and Staphylococcus aureus with ZOI values of 24.3, 21.8, and 22.1 mm, respectively. Consequently, it demonstrates the substantial potential of rGO-P nanocomposite in the effective removal of pollutant dyes as well as significant antibacterial and antifungal properties.

This research investigates a novel nanocomposite material composed of reduced graphene oxide (rGO) and nickel-5,15-bisdodecylporphyrin (Ni-BDP) nanoparticles for the effective removal of methyl orange (MO), a harmful synthetic dye, from water. The structure and composition of the synthesized rGO/Ni-BDP nanocomposite were characterized using high-resolution transmission electron microscopy (HR-TEM), Raman spectroscopy, nuclear magnetic resonance (NMR) spectroscopy, mass spectrometry, and ultraviolet-visible (UV-Vis) spectroscopy. The study demonstrates the material’s efficacy as both a catalyst and adsorbent for MO removal. Optimal performance was observed at pH 3.0, where the positively charged nanocomposite surface facilitated strong interactions with negatively charged MO molecules, leading to enhanced photocatalytic activity. Under these conditions, 0.01 g of the nanocomposite achieved an impressive 86.2% MO removal efficiency. Furthermore, the study explored the reusability of the rGO/Ni-BDP nanocomposite in repeated cycles of photocatalytic MO degradation under visible light irradiation. While exhibiting some decrease in efficiency over five cycles, the nanocomposite maintained a respectable degradation rate even after multiple uses. Finally, the antimicrobial properties of the nanocomposite were evaluated against both Gram-negative ( Escherichia coli ) and Gram-positive ( Staphylococcus aureus ) bacteria exhibiting a zone of inhibition measuring 23 mm and 26, respectively. The minimum inhibitory concentration (MIC) values of 2.50 µg/ml and 1.25 µg/ml for Escherichia coli and Staphylococcus aureus , respectively. The results revealed significant antibacterial activity, demonstrating the broad-spectrum efficacy of the rGO/Ni-BDP nanocomposite. This research underscores the potential of the rGO/Ni-BDP nanocomposite as a versatile material for environmental remediation and antibacterial applications.

The current work describes a novel route for preparation of robust polymeric monolithic structures exhibiting magnetic properties via emulsification of a polar glycerin oil in a polymerizable hydrophobic oil of styrene as oil/oil (o/o) emulsion technique. Hydrophilic magnetite nanoparticles were first prepared via the co-precipitation method and then converted to organophilic using oleic acid as a surface coating material. The FT-IR provided evidence on the covering of the particle’s surface and also revealed some hydrophilic OH groups co-exist, implying a probable amphiphilic character is acquired. The organophilic particles act efficiently as Pickering stabilizers for glycerin/styrene emulsion systems. Styrene, a polymerizable oil, could be subsequently polymerized at 70 °C in the presence of an oil-soluble thermal initiator such as 1,1-azobiscyclohexanecarbonitrile (vazo). Scanning electron microscopy (SEM) confirmed the formation of well-defined, highly porous polymeric monoliths, in which the distribution of the pores within the monolith further supported that they were prepared via well-emulsified glycerin drops in the styrene phase as a precursor. Additionally, the EDX revealed the presence of the iron element distributed evenly within the monolith. The thermogravimetric analysis (TGA) revealed a slight resistance to thermal degradation over a narrow range up to 150 °C with respect to pure polystyrene, whereas beyond this temperature the degradation behavior proceeded almost typically as for pure polystyrene. The ferromagnetic resonance spectroscopy (FMR) indicated the acquisition of the magnetic property by the produced monolith structure. For the best of our knowledge, it is the first article of its type investigating the fabrication of polymeric monolithic structures from non-aqueous emulsions.

Steel pipeline systems carry about three-quarters of the world’s oil and gas. Such pipelines need to be coated to prevent corrosion and erosion. An alternative to the current epoxy-based coating, a multi-layered composite coating is developed in this research. The composite coatings were made from carbon fiber-reinforced thermoplastic polymer (CFRTP) material. Uniaxial carbon fiber CF/PPS prepreg tape was utilized, where the PPS (polyphenylene sulfide) is employed as a thermoplastic (TP) matrix. Compression molding was used to manufacture three flat panels, each consisting of seven plies: UD (Unidirectional), Biaxial, and Off-axis. Samples of carbon steel were coated with multi-layered composites. The physical, mechanical, and corrosion-resistant properties of steel-composite coated samples were evaluated. A better and more promising lap-shear strength of about 58 MPa was demonstrated. When compared to the Biaxial and Off-axis samples, the UD assembly had the maximum flexural strength (420 MPa); however, the Biaxial coating has the highest corrosion resistance (445 kΩ·cm2) when compared to the Off-axis and UD coatings.

A series of thiosemicarbazone (TSCN) compounds including ((E)-2-((E)-1-(2-(p-tolyl)hydrazono)propan-2-ylidene)hydrazine-1-carbothioamide (TSC1), (E)-N-ethyl-2-((E)-1-(2-(p-tolyl)hydrazono)propan-2-ylidene)hydrazine-1-carbothioamide (TSC2), and (E)-N-phenyl-2-((E)-1-(2-(p-tolyl)hydrazono)propan-2-ylidene)hydrazine-1-carbothioamide) (TSC3) were synthesized and fully characterized by diverse spectroscopies, such as X-ray single-crystal, infrared, mass, proton nuclear magnetic resonance, and ultraviolet-visible. Potentiometric measurements, molecular modeling, and biological and antitumor activity screening were studied. The thermodynamics and protonation constants of TSC1 as a representative of the synthesized TSCs were calculated and discussed. The solution speciation of different species was studied with pH. The molecular parameters of the optimized structures were calculated and discussed. The X-ray single crystals of TSC2 and TSC3 were established. Considering the antimicrobial activities and correlating structure-activity relationship of the synthesized compounds, the TSC1 molecule was considered a promising candidate as an antifungal agent against Candida albicans. Thus, it would be extremely helpful in the field of medicinal chemistry, particularly as an antimicrobial agent. The results are of significance to the chemistry of antimicrobial agents.

Polystyrene microspheres were prepared in magnetized form using a modified route of suspension polymerization in which a type of surface-active agent (Hitenol BC-20), that does not affect the interfacial tension significantly, was involved as stabilizer. In such a way, it helps to provide stabilization to styrene monomer drops in a micronized size into an aqueous phase while preserving the size and shape during the course of conducting the polymerization. Particularly, in case the monomer phase contained dispersed organophilic particles of iron oxide; the successful proceeding of such strategy is ensured from the produced uniform size of the microspheres and stable magnetic property. The excellent and stable ferromagnetism acquired by the spheres indicates a good distribution of a small amount of oleophilized nanoparticles. The produced polymer microspheres are expected for potential applications, i.e., diagnostic devices as well as smart materials Graphic abstract

The introduction of activated carbon/natural zeolite (AC/NZ) as an efficient and reliable nanoadsorbent for enhancing methylene blue (MB) dye adsorption. By calcining sugarcane waste at various temperatures between 500 and 900 °C, activated carbons (ACs) are formed. Both XRD and SEM were used for the characterization of the prepared adsorbents. Adsorption measurements for the removal of MB dye were made on the impact of pH, beginning MB concentration, and contact time. The maximum AC500/NZ adsorption capacity for MB dye at 25 °C, pH 7, and an AC500/NZ mass of 50 mg was found to be approximately 51 mg/g at an initial concentration of 30 ppm. The pseudo-second-order kinetics model and the Temkin isotherm model describe the adsorption process. The Temkin model shows that the adsorption energy is 1.0 kcal/mol, indicating that the MB-to-AC500/NZ adsorption process occurs physically. Our Monte Carlo (MC) simulation studies supported our findings and showed that the Van der Waals dispersion force was responsible for the MB molecule's physical adsorption. The AC500/NZ adsorbent is thought to be a strong contender for water remediation.

A comprehensive study that combined both experimental and computational experiments was performed to evaluate the usage of organo-metal oxide nanocomposite for the elimination of disperse red 60 dye (DR) from aqueous solutions. Chitosan was modified by Schiff base to form nanoneedles chitosan-4-chloroacetophenone derivative. The derivatives were then impregnated with CeO 2 –CuO–Fe 2 O 3 or CeO 2 –CuO–Al 2 O 3 metal oxides to prepare a novel quarternary organo-metal oxide nanocomposite. The novel nanocomposite, chitosan-4-chloroacetophenone/CeO 2 –CuO–Fe 2 O 3 (CF) and chitosan-4-chloroacetophenone/CeO 2 –CuO–Al 2 O 3 (CA) are cheap and effective nano adsorbents that can be used for the uptake of DR from aqueous solution. The CF and CA nano-composites were characterized using different techniques. Moreover, the effect of adsorption parameters (initial DR concentration, time of contact, pH, temperature, and adsorbent mass) as well as CA and CF reusability tests were performed. Langmuir adsorption isotherm and pseudo-second-order kinetics models were best fitted with the adsorption process. The maximum amount of DR adsorbed was 100 mg/g on CF and CA at pH 2 and 4, respectively with a physical spontaneous, and exothermic adsorption process. Monte Carlo ( MC) simulation studies indicated the adsorption of DR molecule on the CF and CA surfaces following a parallel mode in most of all studied configurations, confirming the strong interactions between the DR and surfaces atoms of CF and CA. The molecular structure analysis of DR dye adsorbed on the surface of CF and CA indicated that the adsorption process related to Van der Waals dispersion force. Consequently, this helps to trap DR dye molecules on the surface of CF and CA (i.e., physical adsorption), which supports our experimental results.