Enhanced sunlight photocatalytic activity and biosafety of marine-driven synthesized cerium oxide nanoparticles.

This contribution presents the biosynthesis, physiochemical properties, toxicity and photocatalytic activity of biogenic CeO2 NPs using, for the first time, marine oyster extract as an effective and rich source of bioreducing and capping/stabilizing agents in a one-pot recipe. CeO2 NPs formation was initially confirmed through the color change from light green to pale yellow and subsequently, their corresponding absorption peak was spectroscopically determined at 310 nm with an optical band-gap of 4.67 eV using the DR-UV technique. Further, XRD and Raman analyses indicated that nanoceria possessed face-centered cubic arrangements without any impurities, having an average crystallite size of 10 nm. TEM and SEM results revealed that biogenic CeO2 NPs was approximately spherical in shape with a median particle size of 15 ± 1 nm. The presence of various bioorganic substances on the surface of nanoparticles was deduced by FTIR and TGA results. It is found that marine-based nanoceria shows no cytotoxic effect on the normal cell, thus indicating their enhanced biocompatibility and biosafety to living organisms. Environmentally, due to energy band gap, visible light-activated CeO2 nanocatalyst revealed superior photocatalytic performance on degradation of methylene blue pollutant with removal rate of 99%. Owing to the simplicity, cost-effectiveness, and environmentally friendly nature, this novel marine biosynthetic route paves the way for prospective applications of nanoparticles in various areas.

Algal magnetic nickel oxide nanocatalyst in accelerated synthesis of pyridopyrimidine derivatives.

This research presents a novel biological route for the biosynthesis of nickel oxide nanoparticles (NiO NPs) using marine macroalgae extract as a reducing and coating agent under optimized synthesis conditions. XRD and TEM analyses revealed that phytosynthesized NiO NPs are crystalline in nature with a spherical shape having a mean particle size of 32.64 nm. TGA results indicated the presence of marine-derived organic constituents on the surface of NiO NPs. It is found that biogenic NiO NPs with BET surface area of 45.59 m2g-1 is a highly efficient catalyst for benign one-pot preparation of pyridopyrimidine derivatives using aqueous reaction conditions. This environmentally friendly procedure takes considerable advantages of shorter reaction times, excellent product yields (up to 96%), magnetically viable nanocatalyst (7 runs), low catalyst loadings, and free toxic chemical reagents.

Synergistic effects of combinatorial chitosan and polyphenol biomolecules on enhanced antibacterial activity of biofunctionalaized silver nanoparticles.

The present study reports the synergistic antibacterial activity of biosynthesized silver nanoparticles (AgNPs) with the aid of a combination of chitosan and seaweed-derived polyphenols as a green synthetic route. Under optimum synthesis conditions, the rapid color change from yellowish to dark brown and UV-visible absorption peak at 425 confirmed the initial formation of AgNPs. DLS, TEM, XRD, and EDX analyses revealed the spherical shape of pure biogenic AgNPs with a mean diameter size of 12 nm ± 1.5 nm, and a face-centered cubic crystal structure, respectively. FTIR and TGA results indicated the significant contribution of chitosan and polyphenol components into silver ions bioreduction and thermal stability of freshly formed AgNPs. Long-term colloidal stability of AgNPs was obtained after 6-month storage at room temperature. The bio-prepared AgNPs possessed a negative surface charge with a zeta potential value of - 27 mV. In contrast to naked chemical silver nanoparticles, the green Ag nanosamples demonstrated the distinct synergistic antibacterial in vitro toward all selected human pathogens presumably due to the presence of high content of biomolecules on their surface. The results show that synergy between chitosan and polyphenol results in the enhancement of bactericidal properties of biogenic AgNPs. We also highlighted the underlying mechanism involved in AgNPs formation based on nucleophile-electrophile interaction.

Selenium functionalized magnetic nanocomposite as an effective mercury (II) ion scavenger from environmental water and industrial wastewater samples.

A novel core-shell magnetic-selenium nanocomposite (Fe3O4@SiO2@Se) was synthesized for fast and effective removal of Hg (II) ions from various industrial and environmental water samples. The composition, property, and structure of Fe3O4@SiO2@Se were characterized by spectral and microscopic techniques. The key parameters affecting the removal were evaluated and optimized. The concentration of residual Hg (II) ions in the solution was measured using a cold vapor atomic absorption spectrometer. At pH = 3.0, Fe3O4@SiO2@Se was capable to remove Hg (II) ions ranged from 100 µg L-1 to 10 mg L-1 within 20 min with the efficiency of approximately 99% in a way that residual concentration levels matched international standards. This level of removal efficiency was well maintained up to salinity of 25 g L-1. Kinetic investigations revealed compliance with a second-order kinetic model. The linear regression coefficient suggested the adsorption of Hg (II) ions by the adsorbent followed the Langmuir isotherm model (R2 > 0.997). The maximum capacity of the adsorbent obtained through investigating the isotherms was 70.42 mg g-1. The Fe3O4@SiO2@Se adsorbent effectively removed the Hg (II) ions spiked to different samples, including tap water, river water, seawater, and industrial wastewater. Therefore, this nano-adsorbent can be used as a good alternative for Hg (II) removal, in practical applications.

Impact of Biocompatible Nanosilica on Green Stabilization of Subgrade Soil.

This study reports the synthesis and potential application of biocompatible silica nanoparticles for subgrade soil stabilization. Nanosilica preparation as a major component from wheat husk ash is systematically studied and confirmed by FTIR, ICP, XRD, and TEM analyses. The produced biogenic nanosilica showed an amorphous structure with an average size of 20 nm. Upon loading various green nanosilica contents, our results show an improvement in the key parameters including Atterberg's limits, maximum dry density, optimum water content, and shear strength of treated soil. Under optimal loading condition, the nanosilica-mediated soil analyses reveal a significant increase in the plastic and liquid limits by factors of 1.60 and 1.24 whereas plasticity index is declined by a factor of 0.78 rather than untreated soil specimen. The treated soil demonstrates a superior increase in the angle of internal friction, cohesion, shear strength, and maximum dry unit weight by factors of 2.17, 3.07, 2.21 and 1.5, respectively. The California Bearing Ratio (CBR) strength of nanosilica-cured soil presents a substantial increase by a factor of 5.83 higher than the corresponding original subgrade soil. We obtained the maximum increase in strength parameters of modified soil at the optimum biogenic nanosilica content of 1.5%.

Phycosynthesis and Enhanced Photocatalytic Activity of Zinc Oxide Nanoparticles Toward Organosulfur Pollutants.

A novel eco-friendly procedure was developed to produce safer, stable and highly pure zinc oxide nanoparticles (ZnO NPs) using microalgae Chlorella extract. The ZnO NPs were synthesized simply using zinc nitrate and microalgae Chlorella extract which conducted at ambient conditions. In this recipe, microalgae Chlorella extract acted as the reducing agent and a stabilizing layer on fresh ZnO NPs. UV-visible spectrum was confirmed the formation of ZnO NPs showing an absorption peak at 362 nm. XRD results demonstrated that prepared ZnO NPs has a high-crystalline hexagonal (Wurtzite) structure, with average size about 19.44 nm in diameter. FT-IR spectral analysis indicated an active contribution of algae-derived biomolecules in zinc ions bioreduction. According to SEM and TEM observations, ZnO NPs are well dispersed and has a hexagonal shape with the average size of 20 ± 2.2 nm, respectively. Based on gas chromatography analyses, the optimum 0.01 g/L dosage of ZnO catalyst revealed an effective photocatalytic activity toward the degradation (97%) of Dibenzothiophene (DBT) contaminant as an organosulfur model in the neutral pH at the mild condition. Rapid separation and facile recyclability at five consecutive runs were demonstrated high efficiency and durability of green ZnO nanophotocatalyst. The possible mechanisms of green ZnO NPs formation and the photo-desulfurization of DBT were also proposed.

Enhanced antibacterial activity, mechanical and physical properties of alginate/hydroxyapatite bionanocomposite film.

The effect of hydroxyapatite nanoparticles (HA NPs) contents on the antibacterial activity, physical, and mechanical properties of sodium alginate (SA) film was scrutinized. The samples were prepared via incorporation of three different concentrations of HA NPs (1%, 3%, and 5%) into alginate solution at ambient temperature. In all SA/HA matrices, HA NPs demonstrated considerable bactericidal activity against foodborne pathogen during 12 days. The highest antibacterial effect of SA film was obtained in the presence of 5%HA NPs content and showed 3 CFU/mg reduction. In comparison to pristine alginate, different HA NPs additives enhanced elongation, tensile strength and moisture content of the nanocomposite films. Moreover, water solubility and water vapor permeability of the bionanocomposite were considerably reduced by 50% as the concentration of HA NPs content up to 5%.

Impact of Pharmaceutical Impurities in Ecstasy Tablets: Gas Chromatography-Mass Spectrometry Study.

In this study, a simple and reliable method by gas chromatograph-mass spectrometry (GC-MS) was developed for the fast and regular identification of 3, 4-MDMA impurities in ecstasy tablets. In so doing, 8 samples of impurities were extracted by diethyl ether under alkaline condition and then analyzed by GC-MS. The results revealed high MDMA levels ranging from 37.6% to 57.7%. The GC-MS method showed that unambiguous identification can be achieved for MDMA from 3, 4-methylenedioxyamphetamine (MDA), Amphetamine (AM), methamphetamine (MA) and ketamine (Keta) compounds, respectively. The experimental results indicated the acceptable time window without interfering peaks. It is found that GC-MS was provided a suitable and rapid identification approach for MDMA (Ecstacy) tablets, particularly in the Forensic labs. Consequently, the intense MDMA levels would support the police to develop a simple quantification of impurity in Ecstasy tablets.