One-pot facile synthesis of hexagonal Bi2Te3 nanosheets and its novel nanocomposites: Characterization, anticancer, antibacterial, and antioxidant activities.

Bismuth Telluride (Bi2Te3) layered structure results in extraordinary features in diagnostic and therapeutic applications. However, Bi2Te3 synthesis with reliable stability and biocompatibility in biological systems was the major challenge that limited its biological application. Herein, reduced graphene oxide (RGO) or graphitic carbon nitride (CN) nanosheets were incorporated into Bi2Te3 matrix to improve exfoliation. Bi2Te3 nanoparticles (NPs) and its novel nanocomposites (NCs): CN@Bi2Te3 and CN-RGO@Bi2Te3 were solvothermally synthesized, physiochemically characterized and assessed for their anticancer, antioxidant, and antibacterial activities. X-ray diffraction depicted Bi2Te3 rhombohedral lattice structure. Fourier-transform infrared and Raman spectra confirmed NC formation. Scanning and transmission electron microscopy revealed 13 nm thickness and 400-600 nm diameter of hexagonal, binary, and ternary nanosheets of Bi2Te3-NPs/NCs. Energy dispersive X-ray Spectroscopy revealed the presence of Bi, Te, and carbon atoms in the tested NPs with negatively charged surfaces as depicted by zeta sizer. CN-RGO@Bi2Te3-NC displayed the smallest nanodiameter (359.7 nm) with the highest Brunauer-Emmett-Teller surface area and antiproliferative activity against MCF-7, HepG2 and Caco-2. Bi2Te3-NPs had the greatest scavenging activity (96.13 ± 0.4%) compared to the NCs. The NPs inhibitory activity was greater against Gram-negative bacteria than that of Gram-positive bacteria. Integration of RGO and CN with Bi2Te3-NPs enhanced their physicochemical properties and therapeutic activities giving rise to their promising capacity for future biomedical applications.

Treatment of hazardous landfill leachate containing 1,4 dioxane by biochar-based photocatalysts in a solar photo-oxidation reactor.

This study investigates a combined photocatalytic and adsorption system to maximize the removal of 1,4 dioxane from hazardous landfill leachate (HLL). The production of transformation products was also investigated to obtain a comprehensive evaluation of the treatment system. Copper/iron doped zinc oxide (Cu-Fe-ZnO) was introduced to biochar to form a hybrid materials and used to treat HLL contaminated with 1,4 dioxane of 355.0 ± 11.7 mg/L. The Cu-Fe-ZnO/biochar removed 93.1 ± 8.7% of 1,4 dioxane at a dose of 0.6 g/L within 90 min, as compared with only 42.7 ± 3.3% by 1.2 g/L of bare biochar within 210 min. The Cu-Fe-ZnO/biochar degraded 1,4 dioxane into ethylene glycol, glycolic acid, and formic acid. The 1,4 dioxane removal mechanisms were investigated using the density functional theory, demonstrating that doping of ZnO with metal atoms (Cu-Fe) narrowed the bandgap from 3.307 eV to 2.736 eV. The enhanced photocatalytic activity of ZnO was also supported by the role of biochar in increasing the reactive species and adsorbing the pollutant molecules. The high degradation efficiency of 1,4 dioxane using small catalyst doses with short reaction times would reduce the treatment cost and improve the system's applicability for treating HLL and industrial effluents.

Garlic capped silver nanoparticles for rapid detection of cholesterol.

A fluorescent biosensor based on garlic (Allium sativum L.) capped Ag nanoparticles (G-Ag NPs) has been synthesized for cholesterol detection. Pristine Ag NPs and G-Ag NPs were synthesized through the chemical reduction process. The effect of different capping agents such as 3-aminopropyltriethoxysilane (APTS), glutathione, 8-hydroxyquinoline, garlic/APTS, garlic/glutathione, and garlic/8-hydroxyquinoline on Ag NPs was evaluated. These NPs were characterized using Fourier transform infrared (FTIR), energy-dispersive X-ray (EDX), X-ray photoelectron spectroscopy (XPS), high-resolution transmission electron microscopy (HRTEM), X-Ray diffraction (XRD), UV-visible spectra, and Zeta potential. The HRTEM micrographs illustrated that Ag NPs with particles size ranging from 2.98 to 14.34 nm were aggregated. G-Ag NPs images showed uniformly distributed spherical particles with particles size from 4.52 to 12.8 nm. The reduction in the plasmonic bands of Ag NPs and G-Ag NPs occurred by 96.4% and 11.7%, respectively after 12 months. The developed sensor for cholesterol based on the fluorescence enhancement had a linear response in a concentration range of 0.4-5.17 mM with a sensitivity of 4.36 Mm-1 and a limit of detection of 0.186 mM. The high selectivity toward cholesterol in presence of different interferes such as glucose, cysteine, glycine, urea, sucrose, nickel, and copper, and their mixture was evaluated. The applicability of this developed sensor for real serum samples was detected with a recovery percentage from 99.1 to 101.3%. Repeatability and reproducibility experiments displayed relative standard deviations (RSD) of 0.88% and 0.62%, respectively.

Synergistic effects of paper mill sludge and sulfonated graphene catalyst for maximizing bio-hydrogen harvesting from sugarcane bagasse de-polymerization.

In this study, hydrogen harvesting from fermentation of sugarcane bagasse (SCB) was promoted by maintaining synergism between sulfonated graphene (SGR) catalyst and paper mill sludge (PMS). The sulfonic acid (-SO3H) groups in the catalyst played a major role in destructing the ß-1,4 glycosidic bonds of sugarcane bagasse, releasing readily biodegradable sugars into the fermentation medium. The cellulose, hemicellulose, and lignin conversion efficiency were improved by 127.5%, 495.0%, and 109.2%, respectively with 20 mgSGR/gVS catalyst addition, compared with the control samples. These values were also higher than those obtained by non-sulfonated graphene catalyst. The hydrogenation of sugarcane bagasse was maximized at a sulfonated graphene catalyst dosage of 60 mgSGR/gVS, providing the highest hydrogen harvesting of 4104 ± 321 mL. This was associated with an increase of the Proteobacteria phyla up to 52.0%, Firmicutes phyla to 13.9%, and Acinetobacter sp. to 39.8% compared with only 37.0%, 11.3% and 11.1% in the control assay respectively. Moreover, sulfonated graphene catalyst supplementation promoted the acetate fermentation reaction pathway by increasing the acetate/butyrate ratio up to 4.1. Nevertheless, elevating the catalyst dosage up to 120 mgSGR/gVS reduced the hydrogen harvesting (1190 ± 92 mL) due to the release of furfural (1.76 ± 0.02 g/L) in the fermentation cultures, deteriorating the microbes' internal composition and metabolism bioactivities. Finally maximizing the hydrogen productivity from sugarcane bagasse is feasible by incorporation of paper mill sludge and sulfonated graphene catalyst at dosage not exceeding 60 mgSGR/gVS. However, investigating the recyclability and disposal of digestate containing sulfonated graphene catalyst and the associated economic feasibility needs more attention in the future.

Fluorescent garlic-capped Ag nanoparticles as dual sensors for the detection of acetone and acrylamide.

In order to protect human health from the adverse impacts of acrylamide and acetone, simple analytical processes are required to detect low concentrations of acrylamide and acetone. Dual functional garlic-capped silver nanoparticles (G-Ag NPs) have been used as fluorescent sensors for acrylamide and acetone. This technique depends on the quenching of the photoluminescence (PL) intensity of G-Ag NPs with the interaction of either acrylamide or acetone. This fluorescent probe presented high selectivity toward acrylamide with a wide linear response of 0.01-6 mM with a limit of detection (LOD) of 2.9 µM. Moreover, this probe also acted as a selective and sensitive fluorescent sensor for the detection of acetone in the range of 0.1-17 mM with LOD of 55 µM. The applicability of G-Ag NPs as a proposed sensor for acrylamide was evaluated using a potato chips sample with a recovery percentage of 102.4%. Acetone concentration is also quantified in human urine samples and the recoveries ranged from 98.8 to 101.7%. Repeatability and reproducibility studies for acrylamide and acetone offered relative standard deviation (RSD) of 0.9% and 1.5%, and 0.77% and 1.1%, respectively.

Sulphonated graphene catalyst incorporation with sludge enhanced the microbial activities for biomethanization of crude rice straw.

Biomethanization of crude rice straw (RS) was enhanced by a coupled effectiveness of sulphonated graphene (SGR) with sludge rich anaerobes (SRA). A reduction of 19.2 ± 1.32% for cellulose, 40.8 ± 3.7% for hemicellulose and 30.8 ± 2.4% for lignin was achieved with addition of SRA after fermentation of 60 days. The abundance of hydrolytic microbes in SRA i.e. Acidobacteria, Bacteroidetes, Chloroflexi and Proteobacteria caused RS structure liquefaction and dissolution. The reduction of cellulose, hemicellulose and lignin boosted to 92.3 ± 1.5, 84.9 ± 3.5 and 97.0 ± 1.8% respectively with SGR catalyst addition of 100 mg/gVS. Reducing sugars, phenols and volatile fatty acids (VFAs) were subsequently utilized by bacteria and archaea species of Methanosphaera, Methanocella, Candidatus Methanoregula, Methanolinea and Methanosaeta. The biogas yield was 92 ± 3.1 mL/gRS and methane content amounted to 68 ± 4.6% % at SGR catalyst of 80 mg/gVS. These findings show the potential of using SRA/SGR to improve the RS fermentation with a novel application for biogas productivity.

Substituents effect on the spectral studies on rutheninum(III) complexes of 5(-4'-derivatives phenyldiazo)-3-phenyl-2-thioxo-4-thiazolidinone.

A novel series of Ru(III) complexes with 5(-4'-derivatives phenyldiazo)-3-phenyl-2-thioxo-4-thiazolidinone (HLn) have been prepared. The ligands and structural composition of complexes were confirmed and characterized by various physico-chemical techniques. The spectral data were utilized to compute the important ligand field parameters B, beta and Dq. The effect of Hamett's constant on the ligand field parameters is also discussed. The spectral and magnetic results commensurate an octahedral environment around the Ru(III) ion. The B-values suggest a strong covalency in the metal-ligand sigma-bond and the Dq-values indicate a medium-strong ligand-field. IR spectra show that the ligand is neutral bidentate forming thereby a six-membered chelating ring and concomitant formation of an intramolecular hydrogen bond. The ligands are present in associated form in solution via intermolecular hydrogen bond and act as neutral bidentate coordinated to ruthenium(III).

Stereochemistry, structural and models of novel 5-(4'-derivatives phenyldiazo)-3-phenyl-2-thioxo-4-thiazolidinone complexes.

Copper(II) and cadmium(II) complexes of 5-(4'-derivatives phenyldiazo)-3-phenyl-2-thioxo-4-thiazolidinone (HLn) were prepared, their compositions and physicochemical properties were characterized by elemental analysis, magnetic suseptibility measurements, and infrared, electronic spectra. The novel complexes have the stoichiometric formulae [Cu(HLn)(OAc)n(H2O)(X)] (OAc = acetate, X = H2O or acetate) and [Cd(L)(OAc)(H2O)], respectively. Elemental analysis and IR spectra denote, that two types of complexes with different octahedral and tetrahedral structure for Cu(II) and Cd(II) ions. I.R. spectra show that the ligand is monobasic/neutral bidentate forming thereby a six-membered chelating ring and concomitant formation of an intramolecular hydrogen bond. The stoichiometeries of these complexes were determined conductometrically and indicated the formation of 1:1 and 1:2 (metal:ligand) complexes.

Structural and models of dioxouranium(VI) with rhodanine azodyes--V.

The synthesis of several new coordination compounds of dioxouranium(VI) heterochelates with bidentate rhodanineazol compounds derived from rhodanine are described. The ligands and uranyl complexes have been charcaterized by various physico-chemical techniques. The bond lengths and the force constants have been calculated from asymmetric stretching frequency of O-U-O group. The infrared spectral studies showed a monobasic bidentate behaviour with the oxygen and azonitrogen donor system. The ligands contain intramolecular hydrogen bonds.