Persulfate assisted photocatalytic and antibacterial activity of TiO2-CuO coupled with graphene oxide and reduced graphene oxide.

Photocatalysts of TiO2-CuO coupled with 30% graphene oxide (GO) were hydrothermally fabricated, which varied the TiO2 to CuO weight ratios to 1:4, 1:2, 1:1, 2:1 and 4:1 and reduced to form TiO2-CuO/reduced graphene oxide (rGO) photocatalysts. They were characterized using XRD, TEM, SEM, XPS, Raman, and DRS technologies. TiO2-CuO composites and TiO2-CuO/GO degrade methylene blue when persulfate ions are present. Persulfate concentration ranged from 1, 2, 4 to 8 mmol/dm-3 in which the highest activity of 4.4 × 10-2 and 7.35 × 10-2 min-1 was obtained with 4 mmol/dm-3 for TiO2-CuO (1:4) and TiO2-CuO/GO (1:1), respectively. The presence of EDTA and isopropyl alcohol reduced the photodegradation. TiO2-CuO coupled with rGO coagulates methylene blue in the presence of persulfate ions and such coagulation is independent of light. The catalyst dosage and the concentration of the dye were varied for the best-performing samples. The antibacterial activity of the synthesized samples was evaluated against the growth of Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa and Klebsiella pneumonia. Ti:Cu (1:2)-GO and Ti:Cu (1:4)-GO had the highest antibacterial activity against K. pneumoniae (16.08 ± 0.14 mm), P. aeruginosa (22.33 ± 0.58 mm), E. coli (16.17 ± 0.29 mm) and S. aureus (16.08 ± 0.88).

In vitro influence of PEG functionalized ZnO-CuO nanocomposites on bacterial growth.

Polyethyleneglycol-coated biocompatible CuO-ZnO nanocomposites were fabricated hydrothermally varying Zn:Cu ratios as 1:1, 2:1, and 1:2, and their antibacterial activity was determined through the well diffusion method against the Gram-negative Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumoniae, and the Gram-positive Staphylococcus aureus. The minimum inhibitory concentration and the minimum bactericidal concentration values of the synthesized samples were determined. Subsequently, the time synergy kill assay was performed to elucidate the nature of the overall inhibitory effect against the aforementioned bacterial species. The mean zone of inhibition values for all four samples are presented. The inhibitory effect increased with increasing concentration of the nanocomposite (20, 40 and 60 mg/ml) on all the bacterial species except for S. aureus. According to the MBC/MIC ratio, ZnO was found to be bacteriostatic for E. coli and P. aeruginosa, and bactericidal for S. aureus and K. pneumoniae. Zn:Cu 2:1 was bactericidal on all bacterial species. A bacteriostatic effect was observed on E. coli and P. aeruginosa in the presence of Zn:Cu 1:1 whereas, it showed a bactericidal effect on S. aureus and K. pneumoniae. Zn:Cu 1:2 exhibited a bacteriostatic effect on E. coli while a bactericidal effect was observed for E. coli, P. aeruginosa, and K. pneumoniae. The metal oxide nanocomposites were found to be more sensitive towards the Gram-positive strain than the Gram-negative strains. Further, all the nanocomposites possess anti-oxidant activity as shown by the DPPH assay.

Kinetics and Thermodynamics Study of Methylene Blue Adsorption to Sucrose- and Urea-Derived Nitrogen-Enriched, Hierarchically Porous Carbon Activated by KOH and H3PO4.

Hierarchically porous nitrogen-enriched carbon materials synthesized by polymerization of sucrose and urea (SU) were activated by KOH and H3PO4 (SU-KOH and SU-H3PO4, respectively). Characterization was undertaken and the synthesized materials were tested for their ability to adsorb methylene blue (MB). Scanning electron microscopic images along with the Brunauer-Emmett-Teller (BET) surface area analysis revealed the presence of a hierarchically porous system. X-ray photoelectron spectroscopy (XPS) confirms the surface oxidation of SU upon activation with KOH and H3PO4. The best conditions for removing dyes utilizing both activated adsorbents were determined by varying the pH, contact time, adsorbent dosage, and dye concentration. Adsorption kinetics were evaluated, and the adsorption of MB followed second-order kinetics, suggesting the chemisorption of MB to both SU-KOH and SU-H3PO4. Times taken to reach the equilibrium by SU-KOH and SU-H3PO4 were 180 and 30 min, respectively. The adsorption isotherm data were fitted to the Langmuir, Freundlich, Temkin, and Dubinin models. Data were best described by the Temkin isotherm model for SU-KOH and the Freundlich isotherm model for SU-H3PO4. Thermodynamics of the adsorption of MB to the adsorbent was determined by varying the temperature in the range of 25-55 °C. Adsorption of MB increased with increasing temperature, suggesting that the adsorption process is endothermic. The highest adsorption capacities of SU-KOH and SU-H3PO4 (1268 and 897 mg g-1, respectively) were obtained at 55 °C. Synthesized adsorbents were effective in removing MB for five cycles with some loss in activity. The results of this study show that SU activated by KOH and H3PO4 are environmentally benign, favorable, and effective adsorbents for MB adsorption.

Fabrication of Naturally Derived Chitosan and Ilmenite Sand-Based TiO2/Fe2O3/Fe-N-Doped Graphitic Carbon Composite for Photocatalytic Degradation of Methylene Blue under Sunlight.

Fabrication of chitosan and ilmenite sand-based novel photocatalysts through the catalytic graphitization of chitosan is reported. Nanocomposites consisted of TiO2, Fe2O3 and Fe nanoparticles dispersed on a nitrogen-doped graphitic carbon framework. The surface area, pore volume and macropore structure of the carbon matrix is disturbed by the heterogeneously distributed nanoparticles. The extent of graphitization expanded with increasing metal loading as indicated by variation in the ID/IG ratio. The nanomaterial's surface consists of Fe3+ and Ti4+, and graphitic, pyridinic and pyrrolic nitrogen were found in the carbon matrix. The band gap values of the composites varied in the 2.06-2.26 eV range. The photocatalytic activity of the synthesized nanomaterials was determined, and the highest rate constant for the photodegradation of methylene blue under sunlight was 4.4 × 10-3 min-1, which resulted with 10 mg/L MB and 25 mg of the best-performing catalyst. The rate constant rose with increasing concentrations of persulfate added to the medium. The rate constant greatly diminished with the addition of isopropyl alcohol as it scavenged hydroxyl radicals. The presence of co-pollutants including Pb2+, rhodamine B, PO43- and Cl- curtailed the rate of reaction. The activity reduced with an increasing number of uses of the catalyst.

Recent Advances in Chitosan-Based Applications-A Review.

Chitosan derived from chitin gas gathered much interest as a biopolymer due to its known and possible broad applications. Chitin is a nitrogen-enriched polymer abundantly present in the exoskeletons of arthropods, cell walls of fungi, green algae, and microorganisms, radulae and beaks of molluscs and cephalopods, etc. Chitosan is a promising candidate for a wide variety of applications due to its macromolecular structure and its unique biological and physiological properties, including solubility, biocompatibility, biodegradability, and reactivity. Chitosan and its derivatives have been known to be applicable in medicine, pharmaceuticals, food, cosmetics, agriculture, the textile and paper industries, the energy industry, and industrial sustainability. More specifically, their use in drug delivery, dentistry, ophthalmology, wound dressing, cell encapsulation, bioimaging, tissue engineering, food packaging, gelling and coating, food additives and preservatives, active biopolymeric nanofilms, nutraceuticals, skin and hair care, preventing abiotic stress in flora, increasing water availability in plants, controlled release fertilizers, dye-sensitised solar cells, wastewater and sludge treatment, and metal extraction. The merits and demerits associated with the use of chitosan derivatives in the above applications are elucidated, and finally, the key challenges and future perspectives are discussed in detail.

Efficient Visible-Light Photocatalysis and Antibacterial Activity of TiO2-Fe3C-Fe-Fe3O4/Graphitic Carbon Composites Fabricated by Catalytic Graphitization of Sucrose Using Natural Ilmenite.

Dyes in wastewater are a serious problem that needs to be resolved. Adsorption coupled photocatalysis is an innovative technique used to remove dyes from contaminated water. Novel composites of TiO2-Fe3C-Fe-Fe3O4 dispersed on graphitic carbon were fabricated using natural ilmenite sand as the source of iron and titanium, and sucrose as the carbon source, which were available at no cost. Synthesized composites were characterized by X-ray diffractometry (XRD), Raman spectroscopy, transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), X-ray fluorescence spectroscopy (XRF), and diffuse reflectance UV-visible spectroscopy (DRS). Arrangement of nanoribbons of graphitic carbon with respect to the nanomaterials was observed in TEM images, revealing the occurrence of catalytic graphitization. Variations in the intensity ratio (I D/I G), L a and L D, calculated from data obtained from Raman spectroscopy suggested that the level of graphitization increased with an increased loading of the catalysts. SEM images show the immobilization of nanoplate microballs and nanoparticles on the graphitic carbon matrix. The catalyst surface consists of Fe3+ and Ti4+ as the metal species, with V, Mn, and Zr being the main impurities. According to DRS spectra, the synthesized composites absorb light in the visible region efficiently. Fabricated composites effectively adsorb methylene blue via π-π interactions, with the absorption capacities ranging from 21.18 to 45.87 mg/g. They were effective in photodegrading methylene blue under sunlight, where the rate constants varied in the 0.003-0.007 min-1 range. Photogenerated electrons produced by photocatalysts captured by graphitic carbon produce O2 •- radicals, while holes generate OH• radicals, which effectively degrade methylene blue molecules. TiO2-Fe3C-Fe-Fe3O4/graphitic carbon composites inhibited the growth of Escherichia coli (69%) and Staphylococcus aureus (92%) under visible light. Synthesized novel composites using natural materials comprise an ecofriendly, cost-effective solution to remove dyes, and they were effective in inhibiting the growth of Gram-negative and Gram-positive bacteria.

Fabrication of TiO2 Spheres and a Visible Light Active α-Fe2O3/TiO2-Rutile/TiO2-Anatase Heterogeneous Photocatalyst from Natural Ilmenite.

High-purity (98.8%, TiO2) rutile nanoparticles were successfully synthesized using ilmenite sand as the initial titanium source. This novel synthesis method was cost-effective and straightforward due to the absence of the traditional gravity, magnetic, electrostatic separation, ball milling, and smelting processes. Synthesized TiO2 nanoparticles were 99% pure. Also, highly corrosive environmentally hazardous acid leachate generated during the leaching process of ilmenite sand was effectively converted into a highly efficient visible light active photocatalyst. The prepared photocatalyst system consists of anatase-TiO2/rutile-TiO2/Fe2O3 (TF-800), rutile-TiO2/Fe2TiO5 (TFTO-800), and anatase-TiO2/Fe3O4 (TF-450) nanocomposites, respectively. The pseudo-second-order adsorption rate of the TF-800 ternary nanocomposite was 0.126 g mg-1 min-1 in dark conditions, and a 0.044 min-1 visible light initial photodegradation rate was exhibited. The TFTO-800 binary nanocomposite adsorbed methylene blue (MB) following pseudo-second-order adsorption (0.224 g mg-1 min-1) in the dark, and the rate constant for photodegradation of MB in visible light was 0.006 min-1. The prepared TF-450 nanocomposite did not display excellent adsorptive and photocatalytic performances throughout the experiment period. The synthesized TF-800 and TFTO-800 were able to degrade 93.1 and 49.8% of a 100 mL, 10 ppm MB dye solution within 180 min, respectively.

Fabrication of r-GO/GO/α-Fe2O3/Fe2TiO5 Nanocomposite Using Natural Ilmenite and Graphite for Efficient Photocatalysis in Visible Light.

Hematite (α-Fe2O3) and pseudobrookite (Fe2TiO5) suffer from poor charge transport and a high recombination effect under visible light irradiation. This study investigates the design and production of a 2D graphene-like r-GO/GO coupled α-Fe2O3/Fe2TiO5 heterojunction composite with better charge separation. It uses a simple sonochemical and hydrothermal approach followed by L-ascorbic acid chemical reduction pathway. The advantageous band offset of the α-Fe2O3/Fe2TiO5 (TF) nanocomposite between α-Fe2O3 and Fe2TiO5 forms a Type-II heterojunction at the Fe2O3/Fe2TiO5 interface, which efficiently promotes electron-hole separation. Importantly, very corrosive acid leachate resulting from the hydrochloric acid leaching of ilmenite sand, was successfully exploited to fabricate α-Fe2O3/Fe2TiO5 heterojunction. In this paper, a straightforward synthesis strategy was employed to create 2D graphene-like reduced graphene oxide (r-GO) from Ceylon graphite. The two-step process comprises oxidation of graphite to graphene oxide (GO) using the improved Hummer's method, followed by controlled reduction of GO to r-GO using L-ascorbic acid. Before the reduction of GO to the r-GO, the surface of TF heterojunction was coupled with GO and was allowed for the controlled L-ascorbic acid reduction to yield r-GO/GO/α-Fe2O3/Fe2TiO5 nanocomposite. Under visible light illumination, the photocatalytic performance of the 30% GO/TF loaded composite material greatly improved (1240 Wcm-2). Field emission scanning electron microscopy (FE-SEM) and high-resolution transmission electron microscopy (HR-TEM) examined the morphological characteristics of fabricated composites. X-ray photoelectron spectroscopy (XPS), Raman, X-ray diffraction (XRD), X-ray fluorescence (XRF), and diffuse reflectance spectroscopy (DRS) served to analyze the structural features of the produced composites.

Influence of Laboratory Synthesized Graphene Oxide on the Morphology and Properties of Cement Mortar.

The introduction of Graphene Oxide (GO), a nanomaterial, has shown considerable promise in improving the mechanical properties of cement composites. However, the reasons for this improvement are not yet fully understood and demand further research. This study aims to understand the effect of laboratory-produced GO, using Tour's method, on the mechanical properties and morphology of cement mortar containing GO. The GO was characterized using Fourier-transform infrared spectroscopy, X-ray Photoelectron Spectroscopy (XRD), X-ray powder diffraction, and Raman spectroscopy alongside Scanning electron microscopy (SEM). This study adopted a cement mortar with GO percentages of 0.02, 0.025, 0.03, 0.035, and 0.04 with respect to the weight of the cement. The presence of GO in cement mortar increased the density and decreased the consistency and setting times. At the optimum of 0.03% GO viscous suspension, the mechanical properties such as the 28-day compressive strength, splitting tensile strength, and flexural strength were enhanced by 41%, 83%, and 43%, respectively. In addition, Brunauer-Emmett-Teller analysis indicates an increase in surface area and volume of micropores of GO cement mortar, resulting in a decreased volume of mesopores. The improvement in properties was due to increased nucleation sites, calcium silicate hydrate (CSH) density, and a decreased volume of mesopores.