A study of AlZn alloys at elevated temperatures by X-ray diffraction

1993 ◽  
Vol 140 (2) ◽  
pp. 341-352 ◽  
Author(s):  
S. Popovic ◽  
B. Gržeta ◽  
H. Löffler ◽  
G. Wendrock
1961 ◽  
Vol 5 ◽  
pp. 276-284
Author(s):  
E. L. Moore ◽  
J. S. Metcalf

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.


CORROSION ◽  
10.5006/3881 ◽  
2021 ◽  
Author(s):  
Zachary Karmiol ◽  
Dev Chidambaram

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.


2002 ◽  
Vol 411 (2) ◽  
pp. 234-239 ◽  
Author(s):  
M Hecker ◽  
W Pitschke ◽  
D Tietjen ◽  
C.M Schneider

1999 ◽  
Vol 556 ◽  
Author(s):  
P. E. Raison ◽  
R. G. Haire ◽  
T. Sato ◽  
T. Ogawa

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.


2006 ◽  
Vol 301 ◽  
pp. 177-180 ◽  
Author(s):  
Yuichiro Kuroki ◽  
Tomoichiro Okamoto ◽  
Masasuke Takata

Copper aluminum disulfide (CuAlS2) powders were synthesized in an evacuated ampoule at elevated temperatures. X-ray diffraction analysis revealed that the powders heated at temperatures higher than 800oC were single-phase CuAlS2. In the cathodoluminescence (CL) spectra measured at room temperature, the powders heated at temperatures higher than 600oC exhibited a visible emission peak at approximately 1.8 eV and a distinct ultraviolet emission peak at 3.45 eV. The powder heated at 700oC showed the maximum intensity of ultraviolet emission which is considered to be associated with excitons.


Materials ◽  
2019 ◽  
Vol 12 (6) ◽  
pp. 923 ◽  
Author(s):  
L. Biondi ◽  
M. Perry ◽  
C. Vlachakis ◽  
Z. Wu ◽  
A. Hamilton ◽  
...  

The reinforced concrete structures that support transport, energy and urban networks in developed countries are over half a century old, and are facing widespread deterioration. Geopolymers are an affordable class of materials that have promising applications in concrete structure coating, rehabilitation and sensing, due to their high chloride, sulphate, fire and freeze-thaw resistances and electrolytic conductivity. Work to date has, however, mainly focused on geopolymers that require curing at elevated temperatures, and this limits their ease of use in the field, particularly in cooler climates. Here, we outline a design process for fabricating ambient-cured fly ash geopolymer coatings for concrete substrates. Our technique is distinct from previous work as it requires no additional manufacturing steps or additives, both of which can bear significant costs. Our coatings were tested at varying humidities, and the impacts of mixing and application methods on coating integrity were compared using a combination of calorimetry, x-ray diffraction and image-processing techniques. This work could allow geopolymer coatings to become a more ubiquitous technique for updating ageing concrete infrastructure so that it can meet modern expectations of safety, and shifting requirements due to climate change.


2015 ◽  
Vol 51 (3) ◽  
pp. 1456-1462 ◽  
Author(s):  
Diana Bachiller-Perea ◽  
Aurélien Debelle ◽  
Lionel Thomé ◽  
Jean-Paul Crocombette

2018 ◽  
Vol 106 (8) ◽  
pp. 655-667
Author(s):  
Shogo Nishikawa ◽  
Taishi Kobayashi ◽  
Takayuki Sasaki ◽  
Ikuji Takagi

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.


2008 ◽  
Vol 72 (1) ◽  
pp. 217-220 ◽  
Author(s):  
H. P. Vu ◽  
S. Shaw ◽  
L. G. Benning

AbstractThe kinetics and mechanisms of the transformation of 2-line ferrihydrite (FH) to hematite (HM), in the presence of Pb at elevated temperatures and high pH condition, were elucidated using synchrotron-based,in situenergy dispersive X-ray diffraction (EDXRD). The time-resolved diffraction data indicated that HM crystallization occurred via a two-stage process. Based on the EDXRD data, combined with high-resolution electron microscopic images, an aqueous-aided 2D growth mechanism is proposed for both HM crystallization stages.


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