scholarly journals Synthesis, Structure, and Properties of EuLnCuSe3 (Ln = Nd, Sm, Gd, Er)

Crystals ◽  
2021 ◽  
Vol 12 (1) ◽  
pp. 17
Author(s):  
Oleg V. Andreev ◽  
Victor V. Atuchin ◽  
Alexander S. Aleksandrovsky ◽  
Yuriy G. Denisenko ◽  
Boris A. Zakharov ◽  
...  
Keyword(s):  
Band Gap ◽  
Optical Band Gap ◽  
Solid Phase ◽  
Measurement Data ◽  
Earth Metal ◽  
Structure Type ◽  
Paramagnetic State ◽  
Solid Phase Reaction ◽  
Phase Reaction ◽  
Space Group

EuLnCuSe3 (Ln = Nd, Sm, Gd, Er), due to their complex composition, should be considered new materials with the ability to purposefully change the properties. Samples of the EuLnCuSe3 were prepared using Cu, rare earth metal, Se (99.99%) by the ampoule method. The samples were obtained by the crystallization from a melt and annealed at temperatures 1073 and 1273 K. The EuErCuSe3 crystal structure was established using the single-crystal particle. EuErCuSe3 crystallizes in the orthorhombic system, space group Cmcm, KCuZrS3 structure type, with cell parameters a = 4.0555 (3), b = 13.3570 (9), and c = 10.4602 (7) Å, V = 566.62 (6) Å3. In structure EuErCuSe3, erbium ions are coordinated by selenium ions in the octahedral polyhedron, copper ions are in the tetrahedral coordination, europium ions are between copper and erbium polyhedra layers and are coordinated by selenium ions as two-cap trigonal prisms. The optical band gap is 1.79 eV. At 4.7 K, a transition from the ferrimagnetic state to the paramagnetic state was detected in EuErCuSe3. At 85 and 293 K, the compound is in a paramagnetic state. According to XRPD data, EuLnCuSe3 (Ln = Nd, Sm, Gd) compounds have a Pnma orthorhombic space group of the Eu2CuS3 structure type. For EuSmCuSe3, a = 10.75704 (15) Å, b = 4.11120 (5) Å, c = 13.37778 (22) Å. In the series of EuLnCuSe3 compounds, the optical band gap increases 1.58 eV (Nd), 1.58 eV (Sm), 1.72 eV (Gd), 1.79 eV (Er), the microhardness of the 205 (Nd), 210 (Sm), 225 (Gd) 235 ± 4 HV (Er) phases increases, and the thermal stability of the phases increases significantly. According to the measurement data of differential scanning calorimetry, the EuNdCuSe3 decomposes, according to the solid-phase reaction T = 1296 K, ΔH = 8.2 ± 0.8 kJ/mol. EuSmCuSe3 melts incongruently T = 1449 K, ΔH = 18.8 ± 1.9 kJ/mol. For the EuGdCuSe3, two (Tα↔β = 1494 K, ΔHα↔β = 14.8 kJ/mol, Tβ↔γ = 1530 K, ΔHβ↔γ = 4.8 kJ/mol) and for EuErCuSe3 three polymorphic transitions (Tα↔β = 1561 K, ΔHα↔β = 30.3 kJ/mol, Tβ↔γ = 1579 K, ΔHβ↔γ = 4.4 kJ/mol, and Tγ↔δ = 1600 K, ΔHγ↔δ = 10.1 kJ/mol). The compounds melt incongruently at the temperature of 1588 K, ΔHmelt = 17.9 ± 1.8 kJ/mol and 1664 K, ΔHmelt = 25.6 ± 2.5 kJ/mol, respectively. Incongruent melting of the phases proceeds with the formation of a solid solution of EuSe and a liquid phase.

The Mixed Lanthanum Dichalcogenide β-LaS1.86(1)Se0.14(1). Synthesis, Crystal Structure, Raman Spectrum and Optical Band Gap

2011 ◽  
Vol 66 (9) ◽  
pp. 873-876
Author(s):  
Christian Bartsch ◽  
Thomas Doert
Keyword(s):  
Crystal Structure ◽  
Raman Spectrum ◽  
Band Gap ◽  
Optical Spectroscopy ◽  
Optical Band Gap ◽  
Structure Type ◽  
Lattice Parameters ◽  
Orthorhombic Space Group ◽  
Space Group ◽  
Lanthanum Sulfide

The ternary lanthanum sulfide selenide β -LaS1.86(1)Se0.14(1) was obtained by reaction of the elements in an NaCl flux. The new compound adopts the β -LnS2 structure type and crystallizes in the orthorhombic space group Pnma (no. 62) with lattice parameters of a = 814.77(1), b = 1638.46(1) and c = 413.88(1) pm. Raman lines indicate the presence of mixed (S1−ySey)2− dianions with y ≈ 0.14, besides the well known S22− dianions. The band gap of β -LaS1.86(1)Se0.14(1) is 2.5 eV as determined by optical spectroscopy.

Synthesis and Characterization of Titania Nanoribbons for Lithium Selective Adsorption

2009 ◽  
Vol 610-613 ◽  
pp. 14-20
Author(s):  
Qin Hui Zhang ◽  
Shao Peng Li ◽  
Shu Ying Sun ◽  
Xian Sheng Yin ◽  
Jian Guo Yu
Keyword(s):  
Solid Phase ◽  
Selective Adsorption ◽  
Adsorption Property ◽  
Hydrothermal Process ◽  
Earth Metal ◽  
Lithium Ion ◽  
Ternary Oxide ◽  
Solid Phase Reaction ◽  
Phase Reaction ◽  
Alkaline Earth Metal Ions

Mesoporous titania nanoribbons are synthesized via an optimized soft hydrothermal process and the derived titania ion-sieves with lithium selective adsorption property are accordingly prepared via a simple solid-phase reaction between Li2CO3 and TiO2 nanomaterials followed by the acid treatment process to extract lithium from the Li2TiO3 ternary oxide precursors. The physical chemistry structure are characterized by XRD, TEM/HRTEM, SAED and N2 adsorption-desorption analysis; and the lithium selective adsorption properties are tested by the adsorption isotherm measurement and demonstrated with the distribution coefficient of a series of alkaline and alkaline-earth metal ions. Though the high temperature calcinations and lithium insertion-extraction process resulted in the agglomeration of nanostructure to large bulky particles, it implied that that the low-dimensional titania nanoribbons might be functionalized to lithium ion-sieves with remarkable adsorption capacity and selectivity, promising in the utilization of lithium extraction from aqueous resources including brine or seawater.

scholarly journals Fe3O4@C Nanoparticles Synthesized by In Situ Solid-Phase Method for Removal of Methylene Blue

Nanomaterials ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 330
Author(s):  
Hengli Xiang ◽  
Genkuan Ren ◽  
Yanjun Zhong ◽  
Dehua Xu ◽  
Zhiye Zhang ◽  
...  
Keyword(s):  
Methylene Blue ◽  
Solid Phase ◽  
Raw Materials ◽  
Phase Method ◽  
Maximum Adsorption Capacity ◽  
High Catalytic Activity ◽  
Solid Phase Reaction ◽  
Phase Reaction ◽  
High Concentrations

Fe3O4@C nanoparticles were prepared by an in situ, solid-phase reaction, without any precursor, using FeSO4, FeS2, and PVP K30 as raw materials. The nanoparticles were utilized to decolorize high concentrations methylene blue (MB). The results indicated that the maximum adsorption capacity of the Fe3O4@C nanoparticles was 18.52 mg/g, and that the adsorption process was exothermic. Additionally, by employing H2O2 as the initiator of a Fenton-like reaction, the removal efficiency of 100 mg/L MB reached ~99% with Fe3O4@C nanoparticles, while that of MB was only ~34% using pure Fe3O4 nanoparticles. The mechanism of H2O2 activated on the Fe3O4@C nanoparticles and the possible degradation pathways of MB are discussed. The Fe3O4@C nanoparticles retained high catalytic activity after five usage cycles. This work describes a facile method for producing Fe3O4@C nanoparticles with excellent catalytic reactivity, and therefore, represents a promising approach for the industrial production of Fe3O4@C nanoparticles for the treatment of high concentrations of dyes in wastewater.

Microstructure and Mechanical Properties of ZrB2/h-BN Multiphase Ceramics by Low-Temperature Reactive Sintering

2016 ◽  
Vol 697 ◽  
pp. 510-514 ◽  
Author(s):  
Feng Rui Zhai ◽  
Ke Shan ◽  
Ruo Meng Xu ◽  
Min Lu ◽  
Zhong Zhou Yi ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Relative Density ◽  
Fracture Strength ◽  
Solid Phase ◽  
Raw Materials ◽  
Solid Phase Reaction ◽  
Phase Reaction ◽  
Microstructure And Mechanical Properties ◽  
Multiphase Ceramics ◽  
Strength And Toughness

In the present paper, the ZrB2/h-BN multiphase ceramics were fabricated by SPS (spark plasma sintering) technology at lower sintering temperature using h-BN, ZrO2, AlN and Si as raw materials and B2O3 as a sintering aid. The phase constitution and microstructure of specimens were analyzed by XRD and SEM. Moreover, the effects of different sintering pressures on the densification, microstructure and mechanical properties of ZrB2/h-BN multiphase ceramics were also systematically investigated. The results show that the ZrB2 was obtained through solid phase reaction at different sintering pressures, and increasing sintering pressure could accelerate the formation of ZrB2 phase. As the sintering pressure increasing, the fracture strength and toughness of the sintered samples had a similar increasing tendency as the relative density. The better comprehensive properties were obtained at given sintering pressure of 50MPa, and the relative density, fracture strength and toughness reached about 93.4%, 321MPa and 3.3MPa·m1/2, respectively. The SEM analysis shows that the h-BN grains were fine and uniform, and the effect of sintering pressure on grain size was inconspicuous. The distribution of grain is random cross array, and the fracture texture was more obvious with the increase of sintering pressure. The fracture mode of sintered samples remained intergranular fracture mechanism as sintering pressure changed, and the grain refinement, grain pullout and crack deflection helped to increase the mechanical properties.

Study of solid-phase reaction between CsNO3 AND V2O5 in the molar ratio 6:5

1980 ◽  
Vol 18 (3) ◽  
pp. 469-476 ◽  
Author(s):  
Ľ. Žúrková ◽  
K. Gáplovská ◽  
V. Suchá
Keyword(s):  
Solid Phase ◽  
Molar Ratio ◽  
Solid Phase Reaction ◽  
Phase Reaction

X-Ray and Magnetic Measurements of TmFeTi2O7

2014 ◽  
Vol 215 ◽  
pp. 470-473 ◽  
Author(s):  
Tamara V. Drokina ◽  
German A. Petrakovskii ◽  
Dmitrii A. Velikanov ◽  
Maksim S. Molokeev
Keyword(s):  
Spin Glass ◽  
Solid Phase ◽  
Magnetic Measurements ◽  
Diffraction Method ◽  
Freezing Temperature ◽  
Solid Phase Reaction ◽  
Phase Reaction ◽  
X Ray Diffraction ◽  
X Ray ◽  
History Of

In this paper we are reported about a peculiarity of the crystal structure and the magnetic state of TmFeTi2O7. The compound TmFeTi2O7 has been synthesizedusing the solid-phase reaction method. Using X-ray diffraction method the disorder in the distribution of the iron ions over five nonequivalent crystal sites was observed, also the populations of the iron atoms positions were determined. We show that below Tf = 6 K the magnetization of TmFeTi2O7 depends on the magnetic history of the sample. There are indications for spin glass state. This results allow us to assume the state of spin glass is realized below freezing temperature Tf = 6 K in TmFeTi2O7.

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