Efficient removal of methylene blue from colored wastewater using magnetite/carbon nanocomposite

In this work, a new nanocomposite based on activated carbon and magnetite (PM) was synthesized and characterized by the most indicated and modern methods. The obtained magnetite/carbon nanocomposite was tested as adsorbent for the removal of Methylene Blue (MB) from colored wastewater. In ortder to elucidate the adsorption mechanism, kinetic and thermodynamic studies were carried out. The high adsorption capacity of the synthesized nanocomposite was highlighted by regeneration and reuse studies in consecutive adsorption/desorption cycles

Adsorption study of phenol and some phenol derivatives on Fe3O4/C nanocomposites

Magnetite/carbon nanocomposites, prepared by a simple combustion synthesis technique, were tested for the removal of phenol and of some phenol derivatives: p-chlorophenol (p-CP), 3-aminophenol (3-AP), p-nitrophenol (p-NP), 2,6-dimethylphenol (DMP) and 2,4,6- trimethylphenol (TMP) from aqueous solutions. The effect of different parameters, including the magnetite/carbon ratio, initial concentration of pollutant and the contact time on the removal efficiency was investigated. The adsorption kinetics was described by the pseudosecond-order model and the equilibrium data were well fitted with the Langmuir isotherm in case of phenol, the Sips isotherm in case of 3-aminophenol and the Redlich-Peterson isotherm in case of p-nitrophenol. The good adsorption capacity and easy separation using a magnet, recommend the magnetite/carbon nanocomposites as promising candidates for the removal of phenol and its derivatives from polluted water

Combustion Synthesis of SrAl₂O₄: Eu²⁺, Dy³⁺ Phosphorescent Pigments for Glow-in-the-Dark Safety Markings

This study deals with SrAl2O4: Eu2+, Dy3+ phosphor pigments prepared by an optimized perchlorate-assisted combustion synthesis and tested for developing glow-in-the-dark safety markings. Recipes with different oxidizer/fuel ratios were designed to create an in-situ reducing-reaction atmosphere and promote Eu3+ → Eu2+ reduction, which is responsible for the specific long-lasting, green emission of the pigments. The obtained data proved the efficiency of glycine-rich mixtures (up to 200% glycine excess), which led to improved optical features, as compared to the reference stoichiometric sample. The best results in terms of emission intensity and decay time were obtained in the case of 100% glycine excess. The sample with optimum emission characteristics was successfully tested in making glow-in-the-dark coatings applied to two different substrates and using pigment concentrations between 10 and 33% weight

Combustion Synthesis of SrAl2O4: Eu2+, Dy3+ Phosphorescent Pigments for Glow-in-the-Dark Safety Markings

This study deals with SrAl2O4: Eu2+, Dy3+ phosphor pigments prepared by an optimized perchlorate-assisted combustion synthesis and tested for developing glow-in-the-dark safety markings. Recipes with different oxidizer/fuel ratios were designed to create an in-situ reducing-reaction atmosphere and promote Eu3+ → Eu2+ reduction, which is responsible for the specific long-lasting, green emission of the pigments. The obtained data proved the efficiency of glycine-rich mixtures (up to 200% glycine excess), which led to improved optical features, as compared to the reference stoichiometric sample. The best results in terms of emission intensity and decay time were obtained in the case of 100% glycine excess. The sample with optimum emission characteristics was successfully tested in making glow-in-the-dark coatings applied to two different substrates and using pigment concentrations between 10 and 33% weight

Adsorption of Anionic Dyes from Wastewater onto Magnetic Nanocomposite Powders Synthesized by Combustion Method

In the present study, new magnetic nanocomposites were successfully prepared by combustion method, characterized by X-ray diffraction, Fourier transform infrared spectroscopy, magnetic measurements, N2 adsorption–desorption thermal analysis, and scanning electron microscopy, and tested as adsorbents for the removal of anionic dyes (Acid Yellow 42 and Acid Red 213) from aqueous solutions. The influence of process variables solution pH, adsorbent dose, initial dye concentration and temperature on the adsorption was evaluated. The best kinetic model that fitted with experimental data was a pseudo-second order model, and the equilibrium data were correlated by Langmuir isotherm model for the investigated dyes. Maximum removal efficiencies of 98.54% and 97.58% was obtained for Acid Yellow 42 and Acid Red 213, respectively, indicating the superior adsorption capacity of the new synthesized magnetic nanocomposites. The thermodynamic parameters indicated the spontaneous and endothermic nature of the adsorption process

Biosynthesis of Iron Oxide Nanoparticles: Physico-Chemical Characterization and Their In Vitro Cytotoxicity on Healthy and Tumorigenic Cell Lines

Iron oxide nanoparticles were synthesized starting from two aqueous extracts based on Artemisia absinthium L. leaf and stems, employing a simplest, eco-friendliness and low toxicity method—green synthesis. The nanoparticles were characterized by powder X-ray diffraction (XRD), Fourier transformed infrared spectroscopy (FT-IR), X-ray fluorescence analysis (XRF), thermal analysis (TG/DSC), and scanning electron microscopy (SEM). Lack of magnetic properties and the reddish-brown color of all the samples confirms the presence of hematite as majority phase. The FTIR bands located at 435 cm−1 and 590 cm−1, are assigned to Fe-O stretching vibration from hematite, confirming the formation of α-Fe2O3 nanoparticles (NPs). The in vitro screening of the samples revealed that the healthy cell line (HaCaT) presents a good viability (above 80%) after exposure to iron oxide NPs and lack of apoptotic features, while the tumorigenic cell lines manifested a higher sensitivity, especially the melanoma cells (A375) when exposed to concentration of 500 µg/mL iron oxide NPs for 72 h. Moreover, A375 cells elicited significant apoptotic markers under these parameters (concentration of 500 µg/mL iron oxide NPs for a contact time of 72 h)

Biologic Impact of Green Synthetized Magnetic Iron Oxide Nanoparticles on Two Different Lung Tumorigenic Monolayers and a 3D Normal Bronchial Model—EpiAirway^TM Microtissue

The present study reports the successful synthesis of biocompatible magnetic iron oxide nanoparticles (MNPs) by an ecofriendly single step method, using two ethanolic extracts based on leaves of Camellia sinensis L. and Ocimum basilicum L. The effect of both green raw materials as reducing and capping agents was taken into account for the development of MNPs, as well as the reaction synthesis temperature (25 °C and 80 °C). The biological effect of the MNPs obtained from Camellia sinensis L. ethanolic extract (Cs 25, Cs 80) was compared with that of the MNPs obtained from Ocimum basilicum L. ethanolic extract (Ob 25, Ob 80), by using two morphologically different lung cancer cell lines (A549 and NCI-H460); the results showed that the higher cell viability impairment was manifested by A549 cells after exposure to MNPs obtained from Ocimum basilicum L. ethanolic extract (Ob 25, Ob 80). Regarding the biosafety profile of the MNPs, it was shown that the EpiAirwayTM models did not elicit important viability decrease or significant histopathological changes after treatment with none of the MNPs (Cs 25, Cs 80 and Ob 25, Ob 80), at concentrations up to 500 µg/mL

Synthesis and Characterization of Bioactive Magnetic Nanoparticles from the Perspective of Hyperthermia Applications

Magnetic iron oxide nanoparticles were obtained for the first time via the green chemistry approach, starting from two aqueous extracts of wormwood (Artemisia absinthium L.), both leaf and stems. In order to obtain magnetic nanoparticles suitable for medical purposes, more precisely with hyperthermia inducing features, a synthesis reaction was conducted, both at room temperature (25 °C) and at 80 °C, and with two formulations of the precipitation agent. Both the quality and stability of the synthesized magnetic iron oxide nanoparticles were physiochemically characterized: phase composition (X-ray powder diffraction (XRD)), thermal behavior (thermogravimetry (TG) and differential scanning calorimetry (DSC)), electron microscopy (scanning (SEM) and transmission (TEM)), and magnetic properties (DC and HF-AC). The magnetic investigation of the as-obtained magnetic iron oxide nanoparticles revealed that the synthesis at 80 °C using a mixture of NaOH and NH3(aq) increases their diameter and implicitly enhances their specific absorption rate (SAR), a mandatory parameter for practical applications in hyperthermia