Solubilities and solubility products of thorium hydroxide under moderate temperature conditions

2018 ◽  
Vol 106 (8) ◽  
pp. 655-667
Author(s):  
Shogo Nishikawa ◽  
Taishi Kobayashi ◽  
Takayuki Sasaki ◽  
Ikuji Takagi
Keyword(s):  
Elevated Temperatures ◽  
Solid Phase ◽  
Size Distributions ◽  
X Ray Diffraction ◽  
X Ray ◽  
Endothermic Process ◽  
Solid Phases ◽  
Solubility Products ◽  
Colloidal Species ◽  
Thorium Hydroxide

AbstractThe Th solubilities of the sample solutions that initially contained Th(OH)4(am) prepared by undersaturation and oversaturation methods in the pHcrange of 2.0–8.0 in a 0.5 M ionic strength solution of NaClO4and HClO4and stored at aging temperatures (Ta) of 298, 313 and 333 K were investigated in this study. After a certain period of time up to 40 weeks depending onTa, supernatants of the sample solutions were ultrafiltrated through 3 kDa membranes under the measurement temperature (Tm) of 298, 313 and 333 K. Size distributions of the colloidal species were investigated by ultrafiltration using membranes with different pore sizes ranging from 3 to 100 kDa, and the solid phases were examined by X-ray diffraction (XRD). The solubility of the sample solutions obtained after aging atTa=298 K using undersaturation method with continuous shaking was similar to those of dried precipitate of Th hydroxide. The solubilities obtained after aging atTa=313 and 333 K were lower than those atTa=298 K. The XRD spectra suggested that the crystallization of the solid phase proceeded under these elevated temperatures. The solubility of the sample solutions obtained after aging atTa=333 K using the oversaturation technique were similar to those prepared by undersaturation method and aged at the sameTa. A slight temperature dependence of the apparent solubilities on theTmwas observed in the sample solutions prepared by both methods. The solubility products$({K_{{\text{sp,}}{T_{\text{a}}}}}({T_{\text{m}}}))$after differentTaandTmwere determined from the solubility analysis. The observed increase in the formation constant$({K_{{\text{s,}}{T_{\text{a}}}}}({T_{\text{m}}}))$of Th4++(4+x)H2O(1)⇌Th(OH)4·xH2O(s,Ta)+4H+with increasingTmindicated that the reaction was endothermic. The enthalpy change$(\Delta_{r}H_{m\_ T_{\text{a}} \to {\text{cr}}}^{\circ} )$between the solid phases of Th(OH)4·xH2O(s,Ta) and ThO2(cr) suggested that the solid phase transformation from Th(OH)4·xH2O(s,Ta) to ThO2(cr) contains an endothermic process.

Solid phase precipitates in (Zr,Th)-OH-(oxalate, malonate) ternary aqueous system

2009 ◽  
Vol 97 (4-5) ◽  
Author(s):  
Taishi Kobayashi ◽  
Takayuki Sasaki ◽  
I. Takagi ◽  
Hirotake Moriyama
Keyword(s):  
Thermal Analysis ◽  
Differential Thermal Analysis ◽  
Solid Phase ◽  
Aqueous System ◽  
Carboxylate Ligand ◽  
X Ray Diffraction ◽  
Large Excess ◽  
X Ray ◽  
Acidic Conditions ◽  
Solid Phases

AbstractThe solubility-limiting solid phases in the ternary aqueous systems of Zr(IV)/OH/oxalate, Zr(IV)/OH/malonate, Th(IV)/OH/oxalate and Th(IV)/OH/malonate were characterized by elemental analysis, X-ray diffraction, thermogravimetric analysis and differential thermal analysis. The ternary solid phase of M(IV)/OH/carboxylate was observed to form, even under acidic conditions, depending on the pH and the concentration of carboxylate ligand. In the presence of a large excess of carboxylic acid, however; the binary M(IV)-carboxylate solid phase formed.

The Application of X-Ray Diffraction at Elevated Temperatures to Study the Mechanism of Formation of Sodium Tripolyphosphate

1961 ◽  
Vol 5 ◽  
pp. 276-284
Author(s):  
E. L. Moore ◽  
J. S. Metcalf
Keyword(s):  
High Temperature ◽  
Low Temperature ◽  
Amorphous Phase ◽  
Elevated Temperatures ◽  
Sodium Tripolyphosphate ◽  
X Ray Diffraction ◽  
Mechanism Of Formation ◽  
X Ray ◽  
Temperature Form ◽  
High Temperature Form

AbstractHigh-temperature X-ray diffraction techniques were employed to study the condensation reactions which occur when sodium orthophosphates are heated to 380°C. Crystalline Na4P2O7 and an amorphous phase were formed first from an equimolar mixture of Na2HPO4·NaH2PO4 and Na2HPO4 at temperatures above 150°C. Further heating resulted in the formation of Na5P3O10-I (high-temperature form) at the expense of the crystalline Na4P4O7 and amorphous phase. Crystalline Na5P3O10-II (low-temperature form) appears after Na5P3O10-I.Conditions which affect the yield of crystalline Na4P2O7 and amorphous phase as intermediates and their effect on the yield of Na5P3O10 are also presented.

scholarly journals ZnOTe Compounds Grown by DC-Magnetron Co-Sputtering

Coatings ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 570
Author(s):  
Olga Sánchez ◽  
Manuel Hernández-Vélez
Keyword(s):  
Molar Fraction ◽  
Variable Parameter ◽  
Point Of View ◽  
X Ray Diffraction ◽  
X Ray ◽  
Sample Series ◽  
Solid Phases ◽  
The One ◽  
High Bulk ◽  
Substrate Sample

ZnOTe compounds were grown by DC magnetron cosputtering from pure Tellurium (Te) and Zinc (Zn) cathodes in O2/Ar atmosphere. The applied power on the Zn target was constant equal to 100 W, while the one applied on the Te target took two values, i.e., 5 W and 10 W. Thus, two sample series were obtained in which the variable parameter was the distance from the Te targets to the substrate. Sample compositions were determined by Rutherford Backscattering Spectroscopy (RBS) experiments. Structural analysis was done using X-Ray diffraction (XRD) spectrometry and the growth of the hexagonal w-ZnO phase was identified in the XRD spectra. RBS results showed high bulk homogeneity of the samples forming ZnOTe alloys, with variable Te molar fraction (MF) ranging from 0.48–0.6% and from 1.9–3.1% for the sample series obtained at 5 W and 10 W, respectively. The results reflect great differences between the two sample series, particularly from the structural and optical point of view. These experiments point to the possibility of Te doping ZnO with the permanence of intrinsic defects, as well as the possibility of the formation of other Te solid phases when its content increases. The results and appreciable variations in the band gap transitions were detected from Photoluminescence (PL) measurements.

Wide angle X-ray diffraction study of the solid-phase chlorinated poly(ethylene)

Polymer ◽  
2004 ◽  
Vol 45 (18) ◽  
pp. 6341-6348 ◽  
Author(s):  
S. Stoeva ◽  
A. Popov ◽  
R. Rodriguez
Keyword(s):  
Diffraction Study ◽  
Solid Phase ◽  
Wide Angle ◽  
X Ray Diffraction ◽  
X Ray ◽  
Poly Ethylene

PREPARATION OF ANTIMONY-PLATINUM SURFACE ALLOY ELECTRODE BY ATOM DIFFUSION IN THE SOLID PHASE

2006 ◽  
Vol 20 (25n27) ◽  
pp. 3999-4004
Author(s):  
HIROSHI MATSUI ◽  
KAZUFUMI WATANABE
Keyword(s):  
Diffraction Pattern ◽  
Low Temperatures ◽  
Solid Phase ◽  
Electrochemical Measurement ◽  
X Ray Diffraction ◽  
Platinum Surface ◽  
X Ray ◽  
Atom Diffusion ◽  
Heat Treated ◽  
Titanium Substrates

Antimony-platinum bilayers were prepared on titanium substrates by the two-step electrodeposition in the usual baths, and then surface alloys were formed by the atom diffusion in the solid phase. The simple antimony layer was little influenced by the substrate in both the measurements of X-ray diffraction and the i - E characteristic in a sulfuric acid solution. Regarding the bilayers, the catalytic activity in hydrogen evolution reaction was very sensitive to the presence of platinum, while the hydrogen adsorbability was quite insensitive. An interaction between antimony and platinum was confirmed by the appearance of a new dissolution wave in the electrochemical measurement and the occurrence of a new diffraction in the X-ray diffraction pattern after the heat-treatment of about 400°C. Although the new diffraction disagreed with any of the reported alloys, clear diffraction pattern of PtSb 2 alloy was observed, when the bilayers were heat-treated at about 600°C for one hour. Considering the penetration depth of X-ray, the alloying of antimony and platinum seems to occur also at low temperatures at least at the top surface.

Oxidation of Alloy-X in Subcritical, Transition, and Supercritical Water

CORROSION ◽  
10.5006/3881 ◽  
2021 ◽  
Author(s):  
Zachary Karmiol ◽  
Dev Chidambaram
Keyword(s):  
Supercritical Water ◽  
Photoelectron Spectroscopy ◽  
Focused Ion Beam ◽  
Elevated Temperatures ◽  
Subcritical Water ◽  
Ion Beam ◽  
X Ray Diffraction ◽  
X Ray ◽  
Nickel Based Superalloy ◽  
Before And After

This work investigates the oxidation of a nickel based superalloy, namely Alloy X, in water at elevated temperatures: subcritical water at 261°C and 27 MPa, the transition between subcritical and supercritical water at 374°C and 27 MPa, and supercritical water at 380°C and 27 MPa for 100 hours. The morphology of the sample surfaces were studied using scanning electron microscopy coupled with focused ion beam milling, and the surface chemistry was investigated using X-ray diffraction, Raman spectroscopy, energy dispersive X-ray spectroscopy, and X-ray photoelectron spectroscopy before and after exposure studies. Surfaces of all samples were identified to comprise of a ferrite spinel containing aluminum.

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.

X-ray diffraction investigations of structural changes in Co/Cu multilayers at elevated temperatures

2002 ◽  
Vol 411 (2) ◽  
pp. 234-239 ◽  
Author(s):  
M Hecker ◽  
W Pitschke ◽  
D Tietjen ◽  
C.M Schneider
Keyword(s):  
Structural Changes ◽  
Elevated Temperatures ◽  
X Ray Diffraction ◽  
X Ray

Fundamental and Technological Aspects of Actinide Oxide Pyrochlores: Relevance For Immobilization Matrices

1999 ◽  
Vol 556 ◽  
Author(s):  
P. E. Raison ◽  
R. G. Haire ◽  
T. Sato ◽  
T. Ogawa
Keyword(s):  
Elevated Temperatures ◽  
Materials Science ◽  
Oxidation Potential ◽  
Oxygen Stoichiometry ◽  
X Ray Diffraction ◽  
X Ray ◽  
Oxidation Reduction ◽  
Reduction Cycle ◽  
Fluorite Type ◽  
The Stability

AbstractPolycrystalline pyrochlore oxides consisting of selected f elements (lanthanides and actinides) and Zr and Hf have been prepared and characterized. Characterization to date has been primarily by X-ray diffraction, both at room and at elevated temperatures. Initial studies concentrated on selected lanthanides and the Np, Pu and Am analogs (reported here) but have been extended to the other actinide elements through Cf. Data from these studies have been used to establish a systematic correlation regarding the fundamental materials science of these particular pyrochlores and structurally related fluorite-type dioxides. In addition to pursuing their materials science, we have addressed some potential technological applications for these materials. Some of the latter concern: (1) immobilization matrices; (2) materials for transmutation concepts; and (3) special nuclear fuel forms that can minimize the generation of nuclear wastes. For f elements that display both a III and IV oxidation state in oxide matrices, the synthetic path required for producing the desired pyrochlore oxide is dictated by their pseudo-oxidation potential the stability of the compound towards oxygen uptake. For the f elements that display an oxidationreduction cycle for pyrochlore-dioxide solid solution, X-ray diffraction can be used to identify the composition in the oxidation-reduction cycle, the oxygen stoichiometry and/or the composition. This paper concentrates on the Np, Pu and Am systems, and addresses the above aspects, the role of the crystal matrix in controlling the ceramic products as well as discussingsome custom-tailored materials.

scholarly journals The Amounts of Water Adsorbed to the Surface of Clay Minerals at the Plastic Limit

2017 ◽  
Vol 64 (3-4) ◽  
pp. 155-162
Author(s):  
Aleksandra Gorączko ◽  
Andrzej Olchawa
Keyword(s):  
Surface Area ◽  
External Surface ◽  
Solid Phase ◽  
Water System ◽  
Basal Spacing ◽  
Plastic Limit ◽  
X Ray Diffraction ◽  
External Surface Area ◽  
X Ray ◽  
Water Layers

AbstractThe paper presents results of a study on the amount of water associated with the solid phase of the clay water system at the plastic limit. Two model monomineral clays, namely kaolinite, and montmorillonite, were used in the study. The latter was obtained by gravitational sedimentation of Na-bentonite (Wyoming).The calculated mean number of water molecule layers on the external surface of montmorillonite was 14.4, and water in interlayer spaces constituted 0.3 of the water mass at the plastic limit.The number of water layers on the external surface of kaolinite particles was 63, which was related to the higher density of the surface electrical charge of kaolinite compared to that of montmorillonite.The calculations were made on the basis of the external surface area of clays and the basal spacing at the plastic limit measured by an X-ray diffraction test. The external surface area of clays was estimated by measuring sorption at a relative humidity p/p0 = 0.5.

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