The Effect of Substituting Ga for Alon Crystal Structure of Phosphors MAl 2Si2O8: Eu2+ (M= Ca, Sr, Ba)

A series of luminescence phosphors M0.955Al2 –xGaxSi2O8∶Eu2+ (M=Ca, Sr, Ba, x = 0~1.0) were prepared via solid-state reaction in weak reductive atmosphere. The lattice positions were discussed. It was found that when Ga3+ entered MAl2Si2O8 lattice and substituted Al3+, complete solid solutions formed. The lattice parameters (a, b, c) and unit cell volume of phosphors M 0.955Al2 –xGaxSi2O8: Eu2+ (M=Ca, Sr, Ba, x = 0~1.0) increased linearly, the lattice parameters (α, β,γ) of Ca0.955Al2–xGaxSi2O8∶Eu2+(CAS) decreased linearly and the lattice parameter β of Sr0.955Al2–xGaxSi2O8∶Eu2+(SAS) and Ba0.955Al2–xGaxSi2O8∶Eu2+(BAS) increased linearly as Ga3+ content increased.

Pt Electrocatalyst Prepared by Hydrothermal Reduction onto the Gas Diffusion Layer for High-Temperature Formic Acid and Ethanol Fuel PEMFC

An alternative method for the preparation of PEMFC electrodes is presented in this work based on the direct deposition of Pt particles onto the gas diffusion layer (Pt@GDL) by hydrothermal reduction of the H2PtCl6 precursor from formic acid, ethylene glycol, and ethanol reductive solutions. There is a successful anchorage of Pt particles via the formation of Pt crystal aggregates. The influence of the reducing agent concentration and temperature was studied to analyze their influence on the size, morphology, and distribution of the Pt particles on the gas GDL. The prepared Pt@GDL was tested for formic acid and ethanol high-temperature H3PO4-doped PEMFC. The Pt@GDL prepared in the formic acid reductive atmosphere presented the best performance associated with the formation of smaller Pt crystals and a more homogeneous dispersion of the Pt particles. For formic acid and ethanol-fed high-temperature PEMFC using a H3PO4-doped polybenzimidazole membrane as the solid electrolyte, maximum power densities of 0.025 and 0.007 W cm−2 were drawn at 200 °C, respectively.

Sintering-Based In-Situ Synthesis and Characterization by TEM of Noble Metal Nanoparticles for Ceramic Glaze Color Control

Gold and silver salt mixtures are incorporated in ceramic glazes for in situ development of mixtures of gold and silver nanoparticles (NPs) that subsequently allow for a wide spectrum of low metal loading color control within ceramic materials. Prior work has shown that gold NPs can be used to create vibrant, color-rich red pigments in high-temperature ceramic and glass applications, though the achievable diameter of the gold NP ultimately limits the available range of color. The current study significantly expands color control from traditional gold nanoparticle red through silver nanoparticle green via the alteration of gold-to-silver salt ratios incorporated in the glaze formulations prior to sintering. Nanoparticle-based coloring systems are tested in both oxidative and reductive firing atmospheres. While the oxidation environment is found to be prohibitive for silver NP stability, the reductive atmosphere is able to form and sustain mixtures of gold and silver NPs across a wide color spectrum. All glazes are analyzed via reflectance spectrometry for color performance and samples are characterized via TEM and EDS for composition and sizing trends. This study creates new groundwork for a color-controlled NP system based on noble metal ratio blends that are both nontoxic and achieved with radically lower metal pigment loading than traditional glazes.

The Formation of Cr-Al Spinel under a Reductive Atmosphere

In the present work, for the first time, the possibility of formation of CrAl2O4 was shown from the equimolar mixture of co-precipitated Al2O3 and Cr2O3 oxides under a reductive environment. The crystallographic properties of the formed compound were calculated using the DICVOL procedure. It was determined that it has a cubic crystal structure with space group Fd-3m and a unit cell parameter equal to 8.22(3) Å. The formed CrAl2O4 is not stable under ambient conditions and easily undergoes oxidation to α-Al2O3 and α-Cr2O3. The overall sequence of the phase transformations of co-precipitated oxides leading to the formation of spinel structure is proposed.

H-USY and H-ZSM-5 zeolites as catalysts for HDPE conversion under a hydrogen reductive atmosphere

This work uses thermogravimetric analysis to investigate the influence of acidity and accessibility in the catalytic conversion of HDPE under hydrogen atmosphere over parent and Ni-based H-USY and H-ZSM-5 zeolites.

Ligand-coordinated Ir single-atom catalysts stabilized on oxide supports for ethylene hydrogenation and their evolution under a reductive atmosphere

Effective, stable, durable, and tunable Ir-ligand single-atom catalysts for ethylene hydrogenation, studied in situ for structural evolution of Ir single-atoms under a reducing atmosphere.

Separation procedures in the identification of the hydrogenation products of biomass-derived hydroxymethylfurfural

Lignocellulosic biomass is considered an attractive and most abundant renewable carbon feedstock. Hydroxymethylfurfural (HMF) is one of the platform molecules obtained from biomass. HMF transformation in the reductive atmosphere allows to obtain numerous value-added molecules with applications in several recently emerged sectors, e.g. biofuels and biopolymers. This process is still intensively investigated, and more efficient, stable and sustainable solutions are envisaged. Therefore, the choice of efficient analytical methods is of great importance. This review covers the methodologies used for the analysis of HMF hydrodeoxygenation, including chromatographic and spectrometric methods. Techniques such as gas chromatography, high-performance liquid chromatography, Fourier transform infrared spectroscopy, nuclear magnetic resonance, and mass spectrometry are mentioned as well in this review.