Impact of Silica Additions on the Phase Composition and Electrical Transport Properties of Ruddlesden-Popper La2NiO4+δ Mixed Conducting Ceramics

The present work explores the possibility of incorporation of silicon into the crystal structure of Ruddlesden-Popper La2NiO4+δ mixed conducting ceramics with the aim to improve the chemical compatibility with lanthanum silicate-based solid electrolytes. Ceramics with the nominal composition La2Ni1−ySiyO4+δ (y = 0, 0.02 and 0.05) were prepared by the glycine nitrate combustion technique and sintered at 1450 °C. While minor changes in the lattice parameters of the tetragonal K2NiF4-type lattice may suggest incorporation of a small fraction of Si into the Ni sublattice, combined XRD and SEM/EDS studies indicate that this fraction is very limited (≪2 at.%, if any). Instead, additions of silica result in segregation of apatite-type La10−xSi6O26+δ and La2O3 secondary phases as confirmed experimentally and supported by the static lattice simulations. Both total electrical conductivity and oxygen-ionic transport in La2NiO4+δ ceramics are suppressed by silica additions. The preferential reactivity of silica with lanthanum oxide opens a possibility to improve the compatibility between lanthanum silicate-based solid electrolytes and La2NiO4+δ-based electrodes by appropriate surface modifications. The promising potential of this approach is supported by preliminary tests of electrodes infiltrated with lanthanum oxide.

Morphology, phase and chemical composition of the nanostructures formed in the systems containing lanthanum, cerium, and silver

X-ray phase and thermogravimetric analysis, scanning electron microscopy and energy-dispersion spectroscopy were used to study the products of phase formation during the precipitation of lanthanum and cerium salts in the presence of silver nitrate and recipients of precipitators, nucleating agents and hydrolysis regulators. Thermogravimetric analysis shows the completion of the La(OH)3 lattice dehydroxylation process at a temperature of ~ 300 °С and probable destruction of sulfates at a temperature of ~ 340 °С. The phase interaction of lanthanum oxide(III) with silver ends at T ~ 400 °C. The DTG curve shows a two-stage weight loss, which characterizes the destruction of lanthanum and silver hydroxides (250 °C) and the removal of sulfates (~ 340 °C), respectively. According to the TG, the total weight loss is 21.6 %. For the cerium-containing system the only endothermic effect of dehydroxylation of cerium hydroxide at T = 250 °C with its conversion into cerium dioxide is observed. The destruction of nitrates (anionic component of solutions) takes place at the temperature of 400 °C. Weight loss takes place at T = 150 °C and is 53.9 %. Thus, on the basis of TG-DTA data, it can be assumed that the formation of composites particles based on lanthanum and cerium oxides, modified with silver, ends at the temperature of 400 °C. The X-ray diffraction data shows that at the initial stage the system undergoes the formation of cerium and lanthanum hydroxides, and during lyophilization of the precipitate (T = 160 °C) the crystal lattice of hydroxides partial dehydroxylation takes place with the formation of trigonal oxides La2O3 and Ce2O3. It has been found that the presence of silver cations in the solution can affect the phase composition of lyophilized structures and the formation of the CeO2 phase. It is shown that the hydroxylamine chloride injection into the system can initiate the silver restoration on the lanthanum oxide surface and also partially restore it to the LaO phase. Temperature treatment of the samples (T = 400 °С) promotes homogenization of the precipitate composition: formation of 30 nm cerium dioxide particles with silver clusters evenly distributed on its surface, and hexagonal lanthanum oxide plates with individual silver particles as the second phase. In three-component systems, two modifications of lanthanum oxides (trigonal and cubic), cerium dioxide and metallic silver are formed. It is found that the chemical composition of the precipitates contains the main elements – La, Ce, O, Ag and impurity – S or Cl, as the anionic component of the initial solutions, N and K in the composition of the initial suspension. It is shown that the morphology of the samples is represented by hexagonal structures of lanthanum hydroxide and oxide, spherical and pseudocubic particles of cerium dioxide and lanthanum oxide, spherical clusters of silver.

Enhancement of Gamma-ray Shielding Properties in Cobalt-Doped Heavy Metal Borate Glasses: The Role of Lanthanum Oxide Reinforcement

The direct influence of La3+ ions on the gamma-ray shielding properties of cobalt-doped heavy metal borate glasses with the chemical formula 0.3CoO-(80-x)B2O3-19.7PbO-xLa2O3: x = 0, 0.5, 1, 1.5, and 2 mol% was examined herein. Several significant radiation shielding parameters were evaluated. The glass density was increased from 3.11 to 3.36 g/cm3 with increasing La3+ ion content from 0 to 2 mol%. The S5 glass sample, which contained the highest concentration of La3+ ions (2 mol%), had the maximum linear (μ) and mass (μm) attenuation coefficients for all photon energies entering, while the S1 glass sample free of La3+ ions possessed the minimum values of μ and μm. Both the half value layer (T1/2) and tenth value layer (TVL) of all investigated glasses showed a similar trend of (T1/2, TVL)S1 > (T1/2, TVL)S2 > (T1/2, TVL)S3 > (T1/2, TVL)S4 > (T1/2, TVL)S5. Our results revealed that the S5 sample had the highest effective atomic number (Zeff) values over the whole range of gamma-ray energy. S5 had the lowest exposure (EBF) and energy absorption (EABF) build-up factor values across the whole photon energy and penetration depth range. Our findings give a strong indication of the S5 sample’s superior gamma-ray shielding characteristics due to the highest contribution of lanthanum oxide.

Lanthanum Oxide Obtention from Different Spent Fluid Catalytic Cracking Catalysts

An laboratory procedure has been developed to obtain lanthanum oxide from spent fluid catalytic cracking catalyst, commonly used in the cracking the heavy crude oil process. Two different spent fluid catalytic cracking catalysts, which are mainly formed by silica and alumina, and a certain amount of rare earths were leached under several conditions to recover the rare earth from the solids waste. Subsequently, liquid phases were subjected to a liquid-liquid extraction process, and lanthanum was quantitatively stripped using oxalic acid to obtain the corresponding lanthanum oxalates. After the corresponding thermal treatment, these solids were transformed into lanthanum oxide. Both, lanthanum oxalates and oxides solids have been characterized by wide techniques in order to investigate the purity of the phases.

Lanthanum Oxide Nickel Hydroxide Composite Triangle Nanosheets for Energy Density Asymmetric Supercapacitors

Transition metal hydroxides are a kind of promising electrode material in electrochemical energy storage, but the poor conductivity limits their application. Lanthanides are good proton conductors and can usually improve the intrinsic conductivity of other materials. By integrating the merits of lanthanide elements and transition metal hydroxide, we designed lanthanum oxide nickel hydroxide composites (LONH) with unique ultrathin triangle nanosheet morphology via a controllable synthetic strategy for high-performance supercapacitors. When the LONH is used as positive electrode material in aqueous asymmetric supercapacitor, it reveals an energy density (107.8 W h kg−1 at 800 W kg−1), rate performance (86.9% retention at 4 kW kg−1) and outstanding cycle stability (more than 90% retention after 3,000 cycles). This work confirms that compositing La2O3 and Ni(OH)2 can significantly improve the supercapacitor performance of both pristine La2O3 and transition metal hydroxide composites. We hope this work would offer a good prospect for developing other lanthanide-transition metal hydroxide composites as an attractive class of electrode materials in electrochemical energy storage.

ED FAGAN MOLYBDENUM LANTHANUM OXIDE

Ed Fagan Molybdenum Lanthanum Oxide, often referred to as lanthanated molybdenum, MoLa or ML, is an oxide dispersion strengthened alloy. It is produced by combining small amounts of lanthanum oxide (La2O3) particles with molybdenum. This creates a special stacked fiber microstructure that is stable at temperatures up to 2000 °C (3630 °F). After recrystallization, the elongated grain structure with jagged grain boundaries provides a measurable increase in ductility and creep resistant strength over that seen with pure molybdenum. Ed Fagan Molybdenum Lanthanum Oxide is the preferred material when embrittlement after recrystallization must be avoided. This alloy maintains its dimensional shape stability at high-temperatures. This datasheet provides information on composition, physical properties, hardness, elasticity, and tensile properties as well as creep. It also includes information on wear resistance as well as heat treating and machining. Filing Code: Mo-21. Producer or source: Ed Fagan Inc.