Structure Differentiation of Hydrophilic Brass Nanoparticles Using a Polyol Toolbox

Nano-brasses are emerging as a new class of composition-dependent applicable materials. It remains a challenge to synthesize hydrophilic brass nanoparticles (NPs) and further exploit them for promising bio-applications. Based on red/ox potential of polyol and nitrate salts precursors, a series of hydrophilic brass formulations of different nanoarchitectures was prepared and characterized. Self-assembly synthesis was performed in the presence of triethylene glycol (TrEG) and nitrate precursors Cu(NO3)2·3H2O and Zn(NO3)2·6H2O in an autoclave system, at different temperatures, conventional or microwave-assisted heating, while a range of precursor ratios was investigated. NPs were thoroughly characterized via X-ray diffraction (XRD), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), transmition electron microscopy (TEM), Fourier-transform infrared (FTIR) spectroscopy, dynamic light scattering (DLS), and ζ-potential to determine the crystal structure, composition, morphology, size, state of polyol coating, and aqueous colloidal stability. Distinct bimetallic α-brasses and γ-brasses, α-Cu40Zn25/γ-Cu11Zn24, α-Cu63Zn37, α-Cu47Zn10/γ-Cu19Zn24, and hierarchical core/shell structures, α-Cu59Zn30@(ZnO)11, Cu35Zn16@(ZnO)49, α-Cu37Zn18@(ZnO)45, Cu@Zinc oxalate, were produced by each synthetic protocol as stoichiometric, copper-rich, and/or zinc-rich nanomaterials. TEM sizes were estimated at 20–40 nm for pure bimetallic particles and at 45–70 nm for hierarchical core/shell structures. Crystallite sizes for the bimetallic nanocrystals were found ca. 30–45 nm, while in the case of the core-shell structures, smaller values around 15–20 nm were calculated for the ZnO shells. Oxidation and/or fragmentation of TrEG was unveiled and attributed to the different fabrication routes and formation mechanisms. All NPs were hydrophilic with 20–30% w/w of polyol coating, non-ionic colloidal stabilization (−5 mV < ζ-potential < −13 mV) and relatively small hydrodynamic sizes (<250 nm). The polyol toolbox proved effective in tailoring the structure and composition of hydrophilic brass NPs while keeping the crystallite and hydrodynamic sizes fixed

Nanostructured Melt-Spun Sm(Co,Fe,Zr,B)7:5 Alloys for High-Temperature Magnets

High coercivity, the highest for Cu-free 2 : 17 Sm-Co ribbons, has been obtained in as-spun (= 211 kOe) and short time annealed (= 232 kOe) samples of Sm(CobalFe Zr B)7 5 alloys, with varying B, Zr, and Fe content (= 0-0 06, = 0-0 16, = 0 08-0 3) and wheel speed. In as-spun samples, the TbCu7 type structure and in annealed samples the Th2Zn17 and CaCu5 type structures is observed, plus fcc Co as minority phase is observed. Reduced remanence () is higher than 0.7. High-temperature magnetic measurements show very good stability above 300 C with coercive field as high as 5.2 kOe at 330 C. For annealed Sm(CobalFe0 3Zr0 02B0 04)7 5, very good loop squareness and high maximum energy product of 10.7 MGOe have been obtained. Increasing Zr content results in less uniform microstructure of annealed ribbons.Comment: IEEE Transactions on Magnetics, Vol. 39, No. 5, pages 2869 - 2871, September 200

Dipolar Energy Anisotropy in Hexagonal Ferrites

The dipolar energy contribution to the anisotropy of M-, W- and Y-type hexagonal ferrites is examined. The geometrical coefficients kij are given, so that a calculation for any hexaferrite with the same structure can be effected. Differences in the results of previous works are explained as due to a simplifying assumption, the validity of which is restricted. The ambiguity regarding dipolar energy anisotropy has been raised: dipolar energy anisotropy is dominant in BaZn-Y, while it is negligible in M- and W-type hexagonal ferrites. The results suggest that single ion anisotropy of the bipyramidal site is significant but the contribution of all the other sites is equally important

Nonstoichiometric Ba Hexaferrites, Prepared by Partial or Complete Ion Exchange

Non-stoichiometric hexaferrite particles (M type structure) in the form of single crystals or fine particles have been prepared by complete or partial ion exchange from β"-ferrite precursor phase. Complete exchange yields directly the hexaferrite phase. Partial exchange maintains the β" structure and heating at T > 600°C is necessary for the M type structure to be formed. The crystal structure of non-stoichiometric hexaferrites is described as an M-type hexaferrite with β-type intergrown cells. The Curie temperature is that of stoichiometric BaFe12O19, Tc=460°C. Saturation magnetization in a field of 20 kOe at room température is 35-65 emu/g and the coercive field Hc ≈ 1.5-2.2 kOe. The higher values are obtained after annealing, which also increases grain size from 50 to 200 nm

A unique ternary Ce(III)-quercetin-phenanthroline assembly with antioxidant and anti-inflammatory properties.

From PubMed via Jisc Publications RouterHistory: received 2022-06-19, revised 2022-07-15, accepted 2022-07-24Publication status: ppublishQuercetin is one of the most bioactive and common dietary flavonoids, with a significant repertoire of biological and pharmacological properties. The biological activity of quercetin, however, is influenced by its limited solubility and bioavailability. Driven by the need to enhance quercetin bioavailability and bioactivity through metal ion complexation, synthetic efforts led to a unique ternary Ce(III)-quercetin-(1,10-phenanthroline) (1) compound. Physicochemical characterization (elemental analysis, FT-IR, Thermogravimetric analysis (TGA), UV-Visible, NMR, Electron Spray Ionization-Mass Spectrometry (ESI-MS), Fluorescence, X-rays) revealed its solid-state and solution properties, with significant information emanating from the coordination sphere composition of Ce(III). The experimental data justified further entry of 1 in biological studies involving toxicity, (Reactive Oxygen Species, ROS)-suppressing potential, cell metabolism inhibition in Saccharomyces cerevisiae (S. cerevisiae) cultures, and plasmid DNA degradation. DFT calculations revealed its electronic structure profile, with in silico studies showing binding to DNA, DNA gyrase, and glutathione S-transferase, thus providing useful complementary insight into the elucidation of the mechanism of action of 1 at the molecular level and interpretation of its bio-activity. The collective work projects the importance of physicochemically supported bio-activity profile of well-defined Ce(III)-flavonoid compounds, thereby justifying focused pursuit of new hybrid metal-organic materials, effectively enhancing the role of naturally-occurring flavonoids in physiology and disease. [Abstract copyright: Copyright © 2022 Elsevier Inc. All rights reserved.

A unique ternary Ce(III)-quercetin-phenanthroline assembly with antioxidant and anti-inflammatory properties

Quercetin is one of the most bioactive and common dietary flavonoids, with a significant repertoire of biological and pharmacological properties. The biological activity of quercetin, however, is influenced by its limited solubility and bioavailability. Driven by the need to enhance quercetin bioavailability and bioactivity through metal ion complexation, synthetic efforts led to a unique ternary Ce(III)-quercetin-(1,10-phenanthroline) (1) compound. Physicochemical characterization (elemental analysis, FT-IR, Thermogravimetric analysis (TGA), UV–Visible, NMR, Electron Spray Ionization-Mass Spectrometry (ESI-MS), Fluorescence, X-rays) revealed its solid-state and solution properties, with significant information emanating from the coordination sphere composition of Ce(III). The experimental data justified further entry of 1 in biological studies involving toxicity, (Reactive Oxygen Species, ROS)-suppressing potential, cell metabolism inhibition in Saccharomyces cerevisiae (S. cerevisiae) cultures, and plasmid DNA degradation. DFT calculations revealed its electronic structure profile, with in silico studies showing binding to DNA, DNA gyrase, and glutathione S-transferase, thus providing useful complementary insight into the elucidation of the mechanism of action of 1 at the molecular level and interpretation of its bio-activity. The collective work projects the importance of physicochemically supported bio-activity profile of well-defined Ce(III)-flavonoid compounds, thereby justifying focused pursuit of new hybrid metal-organic materials, effectively enhancing the role of naturally-occurring flavonoids in physiology and disease

COMPOSITION, MAGNETIC PROPERTIES AND STRUCTURES OF TWO TYPES OF HEXAGONAL FERRITES : Zn SUBSTITUTED SrMn2-W AND BaCo-Y

The magnetic properties of Sr (ZnxMnl-x)2 Fe16O27 (x = 0, 0.33, 0.5) and Ba2Co2Fe12O22 are examined. From neutron diffraction data the composition and cationic distribution are determined. Zn2+ and Mn2+ are in the tetrahedral sites of S, while Co2+ enter preferentially the octahedral sites between S and T blocks. The magnetic structures of the W-type compounds are collinear