scholarly journals Structure feature of ternary state diagrams of Cr-Ti-V and Cr-Mn-V systems

2018 ◽  
Vol 243 ◽  
pp. 00014 ◽  
Author(s):  
Anatoliy Klopotov ◽  
Irina Kurzina ◽  
Alexander Potekaev ◽  
Artem Ustinov ◽  
Taras Dement ◽  
...  

This paper presents the research results of features of structural and phase states in Cr-Ti-V and Cr-Mn-V systems based on analysis of crystal-geometric and crystal-chemical factors. The diagrams of isothermal sections of state diagrams of Cr-Ti-V and Cr-Mn-V systems were built in coordinates of the electron number (s+d) per atom with homogeneity regions of solid solutions and intermetallic compounds. It was shown that in the Cr-Ti-V system, addition of Mn atoms leads to substantial extension of the existence domain of the disordered solid solution based on the BCC lattice.

2004 ◽  
Vol 59 (8) ◽  
pp. 893-897 ◽  
Author(s):  
Mar’yana Lukachuk ◽  
Yaroslav M. Kalychak ◽  
Rainer Pöttgen

AbstractThe thulium nickel indide TmNiIn forms solid solutions TmNi1−x−yIn1+x. Several samples have been prepared by arc-melting of the elements under argon. The structure of TmNiIn contains two crystallographically different nickel sites. The Ni1 atoms have a trigonal prismatic coordination by indium, while the Ni2 sites have six thulium neighbors in a trigonal prismatic arrangement. The Ni1 sites show defects in the solid solution, while the Ni2 sites have Ni2/In mixing with a maximal occupancy of 32 at.-% indium. The structures of three single crystals of solid solutions have been refined, leading to the compositions TmNi0.88In1.10 (a =747.06(7), c = 367.8(1) pm, wR2 =0.0342, 323 F2 values, 16 variables), TmNi0.80In1.16 (a= 752.94(7), c =366.5(1) pm, wR2=0.0475, 503 F2 values, 16 variables), and TmNi0.76In1.21 (a = 758.4(1), c = 366.68(7) pm, wR2 = 0.0949, 226 F2 values, 16 variables). The crystal chemical peculiarities and the differences in chemical bonding are briefly discussed.


1996 ◽  
Vol 60 (402) ◽  
pp. 751-758 ◽  
Author(s):  
Giancarlo Della Ventura ◽  
Annibale Mottana ◽  
Gian Carlo Parodi ◽  
Mati Raudsepp ◽  
Fabio Bellatreccia ◽  
...  

AbstractThe crystal-chemical relationships occurring within a single grain of monazite-(Ce) from Vetralla, Vico Volcanic Complex, north of Rome, are outlined. The sample is from a miarolitic cavity in a holocrystalline ejectum consisting of K-feldspar plus minor plagioclase, mica and Fe-oxides, collected from a pyroclastic explosive level. The Gandolfi film (Cu-Kα radiation) can be indexed in space group P21/n with a = 6.816(4); b = 6.976(4); c = 6.471(3) Å; β = 103.63(3)°; V = 299.0(6) Å3. Electron-probe microanalyses plot within the field of monazite along the huttonite-monazite edge of the huttonite-monazite-brabantite triangle. Despite patchy and irregular zoning, the grain shows a clear enrichment towards pure monazite at the outer rim. A constant Th:Si ratio of 1:1 indicates the existence of a simple solid-solution between huttonite and monazite. The substitution can be written as Th4+ + Si4+ → REE3+ + P5+ without requiring any electrostatic compensation by divalent cations, or by anionic groups. The REE distribution pattern is compatible with that of monazites from syenitic rocks.


Metals ◽  
2018 ◽  
Vol 8 (11) ◽  
pp. 958 ◽  
Author(s):  
Cuiping Wang ◽  
Xianjie Zhang ◽  
Lingling Li ◽  
Yunwei Pan ◽  
Yuechao Chen ◽  
...  

The phase equilibria of the Co-Ti-Ta ternary system at 1000 °C, 1100 °C, and 1200 °C were experimentally investigated using an electron probe microanalyzer and X-ray diffraction. Experimental results show that: (1) No ternary compound exists in the studied isothermal sections; (2) the β(Ti) and β(Ta) phases form the continuous solid solution β(Ti,Ta) in the Ti-Ta side; (3) the solubility of Ta in the (αCo) is less than 5%; (4) the phases of Co2Ti(h) and γ-Co2Ta, Co2Ti(c) and β-Co2Ta form the continuous solid solutions Co2(Ta,Ti)(h) and Co2(Ta,Ti)(c), respectively.


Catalysts ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 640
Author(s):  
Hideaki Sasaki ◽  
Keisuke Sakamoto ◽  
Masami Mori ◽  
Tatsuaki Sakamoto

CeO2-based solid solutions in which Pd partially substitutes for Ce attract considerable attention, owing to their high catalytic performances. In this study, the solid solution (Ce1−xPdxO2−δ) with a high Pd content (x ~ 0.2) was synthesized through co-precipitation under oxidative conditions using molten nitrate, and its structure and thermal decomposition were examined. The characteristics of the solid solution, such as the change in a lattice constant, inhibition of sintering, and ionic states, were examined using X-ray diffraction (XRD), scanning electron microscopy–energy-dispersive X-ray spectroscopy (SEM−EDS), transmission electron microscopy (TEM)−EDS, and X-ray photoelectron spectroscopy (XPS). The synthesis method proposed in this study appears suitable for the easy preparation of CeO2 solid solutions with a high Pd content.


2020 ◽  
Vol 58 (1) ◽  
pp. 71-83
Author(s):  
Elahe Mansouri Gandomani ◽  
Nematollah Rashidnejad-Omran ◽  
Amir Emamjomeh ◽  
Pietro Vignola ◽  
Tahereh Hashemzadeh

ABSTRACT Turquoise, CuAl6(PO4)4(OH)8·4H2O, belongs to the turquoise group, which consists of turquoise, chalcosiderite, aheylite, faustite, planerite, and UM1981-32-PO:FeH. In order to study turquoise-group solid solutions in samples from the Neyshabour and Meydook mines, 17 samples were selected and investigated using electron probe microanalysis. In addition, their major elements were compared in order to evaluate the feasibility of distinguishing the provenance of Persian turquoises. The electron microprobe data show that the studied samples are not constituted of pure turquoise (or any other pure endmember) and belong, from the chemical point of view, to turquoise-group solid solutions. In a turquoise–planerite–chalcosiderite–unknown mineral quaternary solid solution diagram, the chemical compositions of the analyzed samples lie along the turquoise–planerite line with minor involvement of chalcosiderite and the unknown mineral. Among light blue samples with varying hues and saturations from both studied areas, planerite is more abundant among samples from Meydook compared with samples from Neyshabour. Nevertheless, not all the light blue samples are planerite. This study demonstrates that distinguishing the deposit of origin for isochromatic blue and green turquoises, based on electron probe microanalysis method and constitutive major elements, is not possible.


2010 ◽  
Vol 65 (12) ◽  
pp. 1516-1520 ◽  
Author(s):  
Wilfried Hermes ◽  
Falko M. Schappacher ◽  
Rainer Pöttgen

The Mo2B2Fe-type intermetallic compounds Gd2Cu2In and Gd2Cu2Mg form a complete set of solid solutions Gd2Cu2In1−xMgx. The a lattice parameter, the Weiss constant and the Curie temperature increase with increasing magnesium content in an almost Vegard-like manner, while the c parameter remains almost constant. All members of the solid solutions show ferromagnetism with TCs between 114 and 80 K.


1994 ◽  
Vol 341 ◽  
Author(s):  
E. S. Hellman ◽  
E. H. Hartford

AbstractMetastable solid-solutions in the MgO-CaO system grow readily on MgO at 300°C by molecular beam epitaxy. We observe RHEED oscillations indicating a layer-by-layer growth mode; in-plane orientation can be described by the Matthews theory of island rotations. Although some films start to unmix at 500°C, others have been observed to be stable up to 900°C. The Mgl-xCaxO solid solutions grow despite a larger miscibility gap in this system than in any system for which epitaxial solid solutions have been grown. We describe attempts to use these materials as adjustable-lattice constant epitaxial building blocks


Author(s):  
Christopher H. Ingles ◽  
John A. Mavrogenes

ABSTRACT Laser ablation-inductively coupled plasma-mass spectrometry was used to traverse hydrothermal vein sphalerite from different ore-forming stages of the Porgera Au-Ag mine, Papua New Guinea. Elements were measured in situ over the growth of crystals to investigate the greatly varying concentrations of cations in sphalerite and their positions in the lattice. Traverse profiles for 16 elements were obtained and aligned to transmitted light images where possible. Each sample contained an array of elements, with many displaying orders of magnitude concentration differences. Results show the simultaneous incorporation of Cu and Sn in sphalerite, as well as Cu and Ag, In and Sn, As and Sb, Fe and Mn, and Cu and Ga. The relation [4Zn2+ ↔ 2Cu+ + Sn2+ + Sn4+] is proposed to explain the 1:1 Cu–Sn correlation. Further relations can be seen, including a Ga “ceiling” or Cu “floor”, where Ga incorporation becomes dependent on Cu concentrations. Furthermore, silver was also observed to correlate with Au, Mn, Ni, Pb, and Bi. Meta-stable solid solutions between pairs such as Cu, Ag; Fe, Mn; As, Sb; and In, Sn are also suggested. Each of these pairs are neighbors on the periodic table of elements, which suggests that simple solid solution can occur, and positive correlations for all four solid solutions were found in one sample alone. While the concept of charge-specific solid solutions in sphalerite has been discussed in the literature with reference to monovalent cations, the results presented herein also indicate solid solutions of higher oxidation states, containing many cations. Furthermore, while cations in charge-specific solid solutions have been proposed to compete for lattice sites in sphalerite, simultaneous in situ coupled concentrations at Porgera suggest otherwise. Cationic substitution equations displaying decimal ratios of each element in solid solution can then provide a novel method to distinguish between solid solution concentrations in different samples. For example, displaying 1:1 ratios of Cu–Ag and Sb–As: [2Zn2+ ↔ (Cu+0.5, Ag+0.5) + (As3+0.5, Sb3+0.5)], or for a 100:1 Fe–Mn ratio: [Zn2+ ↔ (Fe2+0.99, Mn2+0.01)].


1990 ◽  
Vol 210 ◽  
Author(s):  
R.I. Smith ◽  
A.R. West

AbstractCrystallographic results on the Li4-3x(Al,Ga)xSiO4 solid solutions are reviewed. The six sets of sites available for Li+ ions fall into two groups. The ‘framework’ sites, which also contain the substitutional Al,Ga ions, appear to have little effect on conductivity. The ‘channel’sites contain varying amounts of Li+ ions and are responsible for the dramatic variations in conductivity with x. There is evidence for the presence of one—dimensional defects, comprising columns of ordered Li+ ions, in both the framework and channel sites. The relative numbers of these linear defects has a large bearing on the solid solution mechanism in the framework sites and their occurrence in the channel sites may be responsible for the low conductivity in stoichiometric Li4SiO4.


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