An in situ microtomography apparatus with a laboratory x-ray source for elevated temperatures of up to 1000 °C

2021 ◽  
Vol 92 (3) ◽  
pp. 033704
Author(s):  
Rongqi Zhu ◽  
Zhaoliang Qu ◽  
Shuo Yang ◽  
Daining Fang
Keyword(s):  
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.


2014 ◽  
Vol 20 (4) ◽  
pp. 1038-1045 ◽  
Author(s):  
Christian D. Damsgaard ◽  
Henny Zandbergen ◽  
Thomas W. Hansen ◽  
Ib Chorkendorff ◽  
Jakob B. Wagner

AbstractSpecimen transfer under controlled environment conditions, such as temperature, pressure, and gas composition, is necessary to conduct successive complementary in situ characterization of materials sensitive to ambient conditions. The in situ transfer concept is introduced by linking an environmental transmission electron microscope to an in situ X-ray diffractometer through a dedicated transmission electron microscope specimen transfer holder, capable of sealing the specimen in a gaseous environment at elevated temperatures. Two catalyst material systems have been investigated; Cu/ZnO/Al2O3 catalyst for methanol synthesis and a Co/Al2O3 catalyst for Fischer–Tropsch synthesis. Both systems are sensitive to ambient atmosphere as they will oxidize after relatively short air exposure. The Cu/ZnO/Al2O3 catalyst, was reduced in the in situ X-ray diffractometer set-up, and subsequently, successfully transferred in a reactive environment to the environmental transmission electron microscope where further analysis on the local scale were conducted. The Co/Al2O3 catalyst was reduced in the environmental microscope and successfully kept reduced outside the microscope in a reactive environment. The in situ transfer holder facilitates complimentary in situ experiments of the same specimen without changing the specimen state during transfer.


2021 ◽  
Vol 2124 (1) ◽  
pp. 012016
Author(s):  
I Goncharov ◽  
M Kovaleva ◽  
M Yapryntsev ◽  
V Sirota

Abstract In this article, new composite coatings ZrB2-35MoSi2-15Al were deposited on the surface of a carbon-carbon composite using a multi-chamber detonation accelerator. The evolution of the phase composition of ZrB2-35MoSi2-15Al coatings was analyzed with differential scanning calorimeter (DSC) and X-ray diffractometry (in situ HT-XRD) at temperatures from room temperature (∼ 25°C) to 1400°C (normal atmosphere and pressure). The coating before annealing according to X-ray diffractometry data is tetragonal (t-ZrO2) and monocline (m-ZrO2) zirconium dioxide, monocline silicon oxide (m-SiO2), hexagonal zirconium diboride (h-ZrB2), tetragonal molybdenum disilicide (t-MoSi2), cubic aluminum (c-Al) and cubic yttrium oxide (c-Y2O3). It was found that the coating crystallizes in m-ZrO2 at 460ºC, and then mullite with rhombic crystal lattice appears at 960ºC. When the temperature reaches 1050ºC the m-ZrO2, ZrSiO4, t-ZrO2, m-SiO2 and mullite phases formed in the coating. At 1400 º C, cubic zirconium dioxide appears in the coating. Experimental results can become the basis for the application of ceramic coating ZrB2-35MoSi2-15Al, which can improve the properties of carbon-carbon composites in an oxygen-containing environment at elevated temperatures.


2019 ◽  
Vol 624 ◽  
pp. A136
Author(s):  
S. P. Thompson ◽  
A. Herlihy ◽  
C. A. Murray ◽  
A. R. Baker ◽  
S. J. Day ◽  
...  

Context. Laboratory analogues can provide physical constraints to the interpretation of astronomical observations of cosmic dust but clearly do not experience the same formation conditions. To distinguish between properties intrinsic to the material and properties imprinted by their means of formation requires extensive characterisation. Aims. Sol–gel methods can produce amorphous silicates with potentially high reproducibility, but often require long drying times (24+ h) at elevated temperatures in air, controlled atmosphere, or vacuum. We investigate the possibility that microwave drying can be used to form amorphous silicate on a timescale of ∼10 min and characterise their structural and spectroscopic properties relative to silicates produced by other drying methods. Methods. Microwave-dried amorphous MgSiO3, Fe0.1Mg0.9SiO3 and Mg2SiO4 are characterised using X-ray powder diffraction, total X-ray scattering, small angle X-ray scattering and mid-IR FTIR spectroscopy, and compared to samples produced from the same gels but dried in-air and under vacuum. The development of crystalline structure in the microwave-dried silicates via thermal annealing up to 999°C is also investigated using in situ X-ray powder diffraction. Results. At the inter-atomic level the silicate structures are largely independent of drying method, however larger-scale structured domains, ranging from a ∼few × 10 Å to ∼100’s Å in size, are observed. These are ordered as mass fractals with discernible variation caused by the drying processes. The mid-IR 10 μm band profile is also found to be influenced by the drying process, likely due to the way removal of water and bonded OH influences the distribution of tetrahedral species. However, microwave drying also allows Fe to be easily incorporated into the silicate structure. In situ annealing shows that for amorphous MgSiO3 crystalline forsterite, enstatite and cristobalite are high temperature phases, while for Mg2SiO4 forsterite crystallises at lower temperatures followed by cristobalite at high temperature. For Fe0.1Mg0.9SiO3 the crystallisation temperature is significantly increased and only forsterite is observed. Crystalline SiO2 may be diagnostic of Mg-rich, Fe-poor grain mineralogies. The results are discussed in relation to the different thermal conditions required for dust to crystallise within protoplanetary disk lifetimes. Conclusions. Sol–gel microwave drying provides a fast and easy method of producing amorphous Mg- and Fe,Mg-silicates of both pyroxene and olivine compositions. Their structure and spectroscopic characteristics although similar to silicates produced using other drying methods, exhibit subtle variations which are particularly manifest spectroscopically in the mid-IR, and structurally over medium- and long-range length scales.


MRS Advances ◽  
2020 ◽  
Vol 5 (29-30) ◽  
pp. 1529-1535 ◽  
Author(s):  
Rijie Zhao ◽  
Jianrong Gao ◽  
Yang Ren

AbstractMelting, solidification and solid-state transformation of the intermetallic Ni3Sn compound were investigated in situ using synchrotron high-energy X-ray diffraction. It was observed that the compound undergoes a hexagonal to cubic transition before melting. In solidification, a disordered cubic phase crystallizes from the liquid at a large undercooling but it is reordered prior to bulk solidification. In melting and solidification, forced or natural flows are active bringing about significant changes of crystal orientations. These in situ observations provided insights into phase transformations of Ni3Sn at elevated temperatures and their roles in formation of metastable microstructure consisting of coarse grains and subgrains.


2008 ◽  
Vol 396-398 ◽  
pp. 595-598 ◽  
Author(s):  
Nicola Döbelin ◽  
Tobias J. Brunner ◽  
Wendelin J. Stark ◽  
Manuel Eggimann ◽  
Martin Fisch ◽  
...  

X-ray amorphous tricalcium-phosphate nanoparticles (ATCP) produced by flame spray synthesis were heat-treated at temperatures between 500 and 1000 °C and analyzed in situ by X-ray powder diffraction. The main phase occurring after crystallisation at 525 °C was α-TCP, minor phases were identified as β-TCP and hydroxyapatite. More elevated temperatures induced crystallite growth and the transformation of α-TCP into β-TCP. Above 900 °C no α-TCP was traceable anymore. α’-TCP was not observed in the experiment. This study shows that nanoparticulate α-TCP can be obtained by thermal treatment of an amorphous TCP nanoparticle in a temperature range where sintering effects such as particle growth and densification are moderate or nearly negligible.


2019 ◽  
Vol 7 (21) ◽  
pp. 13364-13371 ◽  
Author(s):  
Xiaoyu Tang ◽  
Jie Zhou ◽  
Miao Bai ◽  
Weiwei Wu ◽  
Shaowen Li ◽  
...  

The lithium ion re-intercalated into the LiMn2O4 lattice during self-discharge.


Minerals ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 297
Author(s):  
Maruša Borštnar ◽  
Christian L. Lengauer ◽  
Sabina Dolenec

The influence of temperature on the early hydration of belite-calcium sulfoaluminate cements with two different calcium sulfate to calcium sulfoaluminate molar ratios was investigated. The phase composition and phase assemblage development of cements prepared using molar ratios of 1 and 2.5 were studied at 25, 40 and 60 °C by in situ X-ray powder diffraction. The Rietveld refinement method was used for quantification. The degree of hydration after 24 h was highest at ambient temperatures, but early hydration was significantly accelerated at elevated temperatures. These differences were more noticeable when we increased the temperature from 25 °C to 40 °C, than it was increased from 40 °C to 60 °C. The amount of calcium sulfate added controls the amount of the precipitated ettringite, namely, the amount of ettringite increased in the cement with a higher molar ratio. The results showed that temperature also affects full width at half maximum of ettringite peaks, which indicates a decrease in crystallite size of ettringite at elevated temperatures due to faster precipitation of ettringite. When using a calcium sulfate to calcium sulfoaluminate molar ratio of 1, higher d-values of ettringite peaks were observed at elevated temperatures, suggesting that more ions were released from the cement clinker at elevated temperatures, allowing a higher ion uptake in the ettringite structure. At a molar ratio of 2.5, less clinker is available in the cement, therefore these differences were not observed.


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