A Ferrofluid with Surface Modified Nanoparticles for Magnetic Hyperthermia and High ROS Production

A ferrofluid with 1,2-Benzenediol-coated iron oxide nanoparticles was synthesized and physicochemically analyzed. This colloidal system was prepared following the typical co-precipitation method, and superparamagnetic nanoparticles of 13.5 nm average diameter, 34 emu/g of magnetic saturation, and 285 K of blocking temperature were obtained. Additionally, the zeta potential showed a suitable colloidal stability for cancer therapy assays and the magneto-calorimetric trails determined a high power absorption density. In addition, the oxidative capability of the ferrofluid was corroborated by performing the Fenton reaction with methylene blue (MB) dissolved in water, where the ferrofluid was suitable for producing reactive oxygen species (ROS), and surprisingly a strong degradation of MB was also observed when it was combined with H2O2. The intracellular ROS production was qualitatively corroborated using the HT-29 human cell line, by detecting the fluorescent rise induced in 2,7-dichlorofluorescein diacetate. In other experiments, cell metabolic activity was measured, and no toxicity was observed, even with concentrations of up to 4 mg/mL of magnetic nanoparticles (MNPs). When the cells were treated with magnetic hyperthermia, 80% of cells were dead at 43 °C using 3 mg/mL of MNPs and applying a magnetic field of 530 kHz with 20 kA/m amplitude.

CDO/CO3O4 NANOCOMPOSITE AS AN EFFICIENT ELECTROCATALYST FOR OXYGEN EVOLUTION REACTION IN ALKALINE MEDIA

Electrochemical water splitting is one of the promising way to enhance energy with less outflow. In this regard different electrocatalysts have been reported for Oxygen evolution reaction (OER) to get alternative of noble metal based electrocatalysts. In this work, we have introduced Cadmium-oxide/Cobalt-oxide (CdO/Co3O4) nanocomposite by co-precipitation chemical strategy with impressive OER performance in alkaline medium. Almost 310 mV overpotential value is required to achieve 10 mA/cm2 current density with Tafel slope value of 62 mV/Dec. The as synthesized nanocomposite has stability of 6h as its longer electrochemical performance

Facile Synthesis of Silane-Modified Mixed Metal Oxide as Catalyst in Transesterification Processes

The fast depletion of fossil fuels has attracted researchers worldwide to explore alternative biofuels, such as biodiesel. In general, the production of biodiesel is carried out via transesterification processes of vegetable oil with the presence of a suitable catalyst. A mixed metal oxide has shown to be a very attractive heterogeneous catalyst with a high performance. Most of the mixed metal oxide is made by using the general wetness impregnation method. A simple route to synthesize silane-modified mixed metal oxide (CaO-CuO/C6) catalysts has been successfully developed. A fluorocarbon surfactant and triblock copolymers (EO)106(PO)70(EO)106 were used to prevent the crystal agglomeration of carbonate salts (CaCO3-CuCO3) as the precursor to form CaO-CuO with a definite size and morphology. The materials show high potency as a catalyst in the transesterification process to produce biodiesel. The calcined co-precipitation product has a high crystallinity form, as confirmed by the XRD analysis. The synthesized catalyst was characterized using Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy-dispersive X-ray (EDX). The mechanism of surface modification and the effects of the catalytic activity were also discussed. The biodiesel purity of the final product was analyzed by gas chromatography. The optimum biodiesel yield was 90.17% using the modified mixed metal oxide CaO-CuO/C6.

Magnetically recyclable silica-coated magnetite-molybdate nanocatalyst and its applications in N-formylation reactions under solvent-free conditions-

A novel magnetite silica-coated nanoparticle-supported molybdate nanocatalyst has been prepared successfully by a simple co-precipitation method. Prepared nanocatalyst has been characterized by different techniques like Fourier Transmission Infrared Spectroscopy (FT-IR), X-ray diffraction (XRD), Field Emission Scanning Electron Microscope (FE-SEM) and Energy Dispersive X-ray Spectroscopy (EDX). Further, the catalytic activity of the nanocatalyst was explored for N-formylation reactions under solvent-free conditions. Interestingly, the catalyst could be reused for 10 cycles and only 2 mol % of the catalyst was sufficient to catalyze the N-formylation reaction at 700C under solvent-free conditions.

Photoelectric and magnetic properties of chemically synthesized Cd-Ni Ferrite nanomagnetic particles

Cadmium nickel (Cd-Ni) ferrite samples have been successfully synthesized via chemical co-precipitation technique. The structural analysis revealed the formation of FCC framework and Fe-phase in a trivalent state. The crystallite size is decreased with increasing Cd2+ ion composition whereas the lattice constant is increased. SEM was used to obtain the surface morphology and average grain size of the microstructure. The FTIR shows the formation of metal oxide, hydroxyl and carboxylic groups. EDX revealed the formation of Ni2+, Cd2+, Fe3+, and O2- ions in proper stoichiometric composition. Large optical losses were revealed by Cd2+ poor-NiFe2O4 samples whereas Cd2+ rich-CdxNi1-xFe2O4 samples revealed low optical losses and showed enhanced photoconductivity and photoelectric effect. Result from optical analysis showed that Cd2+ rich-CdxNi1-xFe2O4 nanoparticles can be used as infrared (IR) detector, ultraviolet (UV) filter and in optoelectronics device applications. VSM measurement showed an increase in saturation magnetization and decrease in coercivity as Cd2+ ion content is increased. The remanance magnetization and magnetic anisotropy were also examined. Photoluminescence (PL) spectroscopy examined the nature of the light emission of the samples at the excitation wavelength 380 nm and emission of series of colours such as red, green, yellow, orange and violet light at different wavelengths were found.

A new transgene mouse model using an extravesicular EGFP tag enables affinity isolation of cell-specific extracellular vesicles

The in vivo function of cell-derived extracellular vesicles (EVs) is challenging to establish since cell-specific EVs are difficult to isolate and differentiate. We, therefore, created an EV reporter using truncated CD9 to display enhanced green fluorescent protein (EGFP) on the EV surface. CD9truc-EGFP expression in cells did not affect EV size and concentration but enabled co-precipitation of EV markers TSG101 and ALIX from the cell-conditioned medium by anti-GFP immunoprecipitation. We then created a transgenic mouse where CD9truc-EGFP was inserted in the inverse orientation and double-floxed, ensuring irreversible Cre recombinase-dependent EV reporter expression. We crossed the EV reporter mice with mice expressing Cre ubiquitously (CMV-Cre), in cardiomyocytes (αMHC-MerCreMer) and renal tubular epithelial cells (Pax8-Cre), respectively. The CD9truc-EGFP positive mice showed Cre-dependent EGFP expression, and plasma CD9truc-EGFP EVs were immunoprecipitated only from CD9truc-EGFP positive CD9truc-EGFPxCMV-Cre and CD9truc-EGFPxαMHC-Cre mice, but not in CD9truc-EGFPxPax8-Cre and CD9truc-EGFP negative mice. In urine samples, CD9truc-EGFP EVs were detected by immunoprecipitation only in CD9truc-EGFP positive CD9truc-EGFPxCMV-Cre and CD9truc-EGFPxPax8-Cre mice, but not CD9truc-EGFPxαMHC-Cre and CD9truc-EGFP negative mice. In conclusion, our EV reporter mouse model enables Cre-dependent EV labeling, providing a new approach to studying cell-specific EVs in vivo and gaining a unique insight into their physiological and pathophysiological function.

Biophotocatalytic Reduction of CO2 in Anaerobic Biogas Produced from Wastewater Treatment Using an Integrated System

This study presents the bio-photocatalytic upgrading of biogas utilising carbon dioxide (CO2) as a potential option for beginning fossil fuel depletion and the associated environmental risks in the pursuit of sustainable development. Herein, magnetite photocatalyst (Fe-TiO2) was employed with an integrated anaerobic-photomagnetic system for the decontamination of municipality wastewater for biogas production. The Fe-TiO2 photocatalyst used, manufactured via a co-precipitation technique, had a specific surface area of 62.73 m2/g, micropore volume of 0.017 cm3/g and pore size of 1.337 nm. The results showed that using the ultraviolet-visible (UV-Vis) photomagnetic system as a post-treatment to the anaerobic digestion (AD) process was very effective with over 85% reduction in colour, chemical oxygen demand (COD) and turbidity. With an organic loading rate (OLR) of 0.394 kg COD/L·d and hydraulic retention time (HTR) of 21 days, a 92% degradation of the organic content (1.64 kgCOD/L) was attained. This maximised the bioenergy production to 5.52 kWh/m3 with over 10% excess energy to offset the energy demand of the UV-Vis lamp. Assuming 33% of the bioenergy produced was used as electricity to power the UV-Vis lamp, the CO2 emission reduction was 1.74 kg CO2 e/m3, with good potential for environmental conservation.

Stabilization of Dicalcium Silicate-Zn Composite Approaching Layered Double Hydroxide Structure for Bioactive Cement Applications

Layered Double Hydroxide (LDH) is ionic clay that is characterized by the union of metal cations and OH- hydroxides. LDH composites exhibit considerably high releasing and recharging capacity and have applications as bioactive cements. They can be prepared by direct co-precipitation of metal salts at controlled pH. The preparation is carried out from an acid solution of Zn (NO3)2.6H2O, Al (NO3)3.9H2O and a basic solution of Na2CO3 and NaOH, with a Zn/Al ratio = 3, the pH is stabilized between 9 and 9.5 at a constant temperature of 45°C. The objective of this study is to incorporate Zinc and Aluminum elements at different percentages in dicalcium silicate phase to produce C2S phase incorporating LDH composite. The characterizations of the developed phases by XRD and SEM indicate the formation of stoichiometric LDH phases Zn6Al2(OH)16CO3.4H2O and non-stoichiometric Zn0.61Al0.39 (OH)2(CO3)0.195.xH2O, the incorporation of Zn in the belitic C2S phase and not Al. The obtained micrographs by SEM(EDAX) analysis show new morphology of the stabilized composite.