scholarly journals Microscopic kinetics of isothermal sintering of Fe-20 % (mаs.) Mo alloy

2021 ◽  
pp. 30-36
Author(s):  
V. Mazur ◽  
Р. Loboda ◽  
Т. Soloviova ◽  
M. Vterkovskyi ◽  
D. Remizov ◽  
...  
Keyword(s):  
Microscopic Analysis ◽  
Phenomenological Theory ◽  
Transformation Rate ◽  
Isothermal Exposure ◽  
X Ray ◽  
Intermediate Phases ◽  
Peritectoid Transformation ◽  
Local Diffusion ◽  
Kinetics Of ◽  
Diffusion Flows

Purpose of work. To investigate the features of microscopic kinetics of peritectoid transformation in Fe-Mo system alloys in an isothermal mode. Experimental part. Microscopic analysis of samples on light (Jenaphot 2000, K. Zeiss) and scanning electron (REM 106I, Selmi) microscopes, X-ray spectral microanalysis of the component’s concentrations distribution between the phases, X-ray phase analysis (Rigaku Ultima IV diffractometer). Results. Microstructure changes, phase composition and crystal lattices parameters of the phase constituents of the powder alloy during sintering at 920 °C were investigated. Variation in the phase constituents mass fraction during 7 hours of the isothermal exposure is analyzed. The formation of anomalous diffusion porosity at the beginning of the process, the nonmonotonic change in the phase constituents fraction and formation of intermediate phases with an unstable component’s concentration are the main features of the microscopic kinetics. The sintering mechanism is proposed. Scientific novelty. A local peritectoid transformation existence at the Fe/Mo interface was established by analyzing the local diffusion flows of components atoms. This transformation occurs upon isothermal supply of Mo atoms with the formation of a cooperative peritectoid structural constituents according to the α- Fe + Mo → α + μ scheme with residual Mo crystals. Formulation of the problem. This work aims to clarify the phenomenological theory of peritectoid transformation during isothermal α-Fe grains enrichment with molybdenum by studying the features of microscopic kinetics in the Fe-Mo system alloys. Practical value. Peritectoid (α + μ) with branched phase соnstituents of cooperative genesis forms a developed system of local diffusion flows of Mo atoms in α -Fe. This increases the molybdenum peritectoid transformation rate at a relatively low sintering temperature for these alloys and reduces the energy consumption in the technological process.

Beobachtungen von Stapelfehlordnungen bei der Oxydation der zweiten zur ersten Stufe des Graphithydrogensulfats / Observation of stacking disorder during the oxidation of second stage to first stage graphite hydrogensulfate

1984 ◽  
Vol 39 (8) ◽  
pp. 768-777 ◽  
Author(s):  
Ko Young Shin ◽  
Hanns-Peter Boehm
Keyword(s):  
Interlayer Spacing ◽  
X Ray Diffraction ◽  
X Ray ◽  
First Order ◽  
Second Stage ◽  
Intermediate Phases ◽  
Degree Of Oxidation ◽  
Stage 1 ◽  
Kinetics Of ◽  
Stacking Disorder

Graphite has been oxidized to graphite hydrogensulfate with (NH4)2S2Og in concentrated H2SO4. The stage 2 compound formed very rapidly, but further oxidation to stage 1 could be followed conveniently. X-ray diffraction of the intermediate phases showed nonintegral (00l)-reflections indicative of partial interstratification disorder. The interlayer spacing of the stage 1 compound increased with continued oxidation. The degree of oxidation as function of oxidation time has been determined from the position of the minima in the reflectance spectra. The density of the compounds and the ratio of acid molecules to anions in the intercalated layers has been estimated using these data and those of buoyancy measurements. There is a minimum in packing density early in the formation of the first stage. The kinetics of intercalation seems to be first order with respect to the free interlayer spaces.

On the stress sensitivity of the dehydration kinetics of gypsum: insights from fast in-situ synchrotron X-ray scattering  

2021 ◽  
Author(s):  
Christoph Schrank ◽  
Oliver Gaede ◽  
Tomasz Blach ◽  
Katherine Gioseffi ◽  
Stephen Mudie ◽  
...  
Keyword(s):  
In Situ Monitoring ◽  
Transformation Rate ◽  
Dehydration Kinetics ◽  
Differential Stress ◽  
X Ray ◽  
Dehydration Rate ◽  
X Ray Scattering ◽  
Kinetics Of ◽  
Ray Scattering

<p>The potential role of differential stress for mineral stability and the kinetics of mineral replacement reactions remains a matter of hot debate. We present a series of unique in-situ laboratory experiments on the dehydration of polycrystalline natural gypsum to hemihydrate, which were designed to test if the application of small differential stresses affects the mineral transformation rate. The dehydration experiments were conducted in a purpose-built loading cell suitable for in-situ monitoring with synchrotron transmission small- and wide-angle X-ray scattering (SAXS/WAXS). The time-resolved SAXS/WAXS data provide measurements of the transformation kinetics and the evolution of nano-pores of the dehydrating samples.</p><p>In our experiments, the kinetic effects of two principal variables were examined: dehydration temperature and axial confinement of the sample discs. In contrast to most previous dehydration experiments conducted in triaxial deformation apparatus, we applied different axial pre-stresses to the radially unconfined sample discs, which were well below the uniaxial compressive strength of the test material. This loading condition corresponds to constant-displacement rather than constant-stress boundary conditions. We find that in natural gypsum alabaster with randomly oriented grains an increase in axial pre-stress leads to a significant acceleration of the dehydration rate. Simple estimates of the energy budget suggest that the acceleration of the dehydration rate due to elastic straining is significantly cheaper energetically than due to heating. We hypothesise that the observed strong effect of differential stress on dehydration kinetics can be explained by geometry-energy interactions in the granular sample microstructure.</p>

Electron Microscopy/Diffraction Study of the Ternary Mn-Er-S System

1990 ◽  
Vol 48 (1) ◽  
pp. 76-77
Author(s):  
A. R. Landa Canovas ◽  
L.C. Otero Diaz ◽  
T. White ◽  
B.G. Hyde
Keyword(s):  
Electron Microscopy ◽  
Gas Flow ◽  
Graphite Crucible ◽  
Nominal Composition ◽  
X Ray Diffraction ◽  
Alumina Crucible ◽  
X Ray ◽  
Intermediate Phases ◽  
Twin Band ◽  
Ar Gas

X-Ray diffraction revealed two intermediate phases in the system MnS+Er2S3,:MnEr2S4= MnS.Er2S3, and MnEr4S7= MnS.2Er2S3. Their structures may be described as NaCl type, chemically twinned at the unit cell level, and isostructural with CaTi2O4, and Y5S7 respectively; i.e. {l13} NaCl twin band widths are (4,4) and (4,3).The present study was to search for structurally-related (twinned B.) structures and or possible disorder, using the more sensitive and appropiate technigue of electron microscopy/diffraction.A sample with nominal composition MnEr2S4 was made by heating Mn3O4 and Er2O3 in a graphite crucible and a 5% H2S in Ar gas flow at 1500°C for 4 hours. A small amount of this material was thenannealed, in an alumina crucible, contained in sealed evacuated silica tube, for 24 days at 1100°C. Both samples were studied by X-ray powder diffraction, and in JEOL 2000 FX and 4000 EX microscopes.

In situ Time-Resolved Small-Angle X-ray Scattering Reveals the Formation Kinetics of Polyelectrolyte Complex Micelles

2019 ◽  
Author(s):  
Hao Wu ◽  
Jeffrey Ting ◽  
Siqi Meng ◽  
Matthew Tirrell
Keyword(s):  
Small Angle ◽  
Self Assembly ◽  
Electrostatic Interactions ◽  
Polyelectrolyte Complex ◽  
Time Resolved ◽  
X Ray ◽  
X Ray Scattering ◽  
Kinetics Of ◽  
Ray Scattering

We have directly observed the <i>in situ</i> self-assembly kinetics of polyelectrolyte complex (PEC) micelles by synchrotron time-resolved small-angle X-ray scattering, equipped with a stopped-flow device that provides millisecond temporal resolution. This work has elucidated one general kinetic pathway for the process of PEC micelle formation, which provides useful physical insights for increasing our fundamental understanding of complexation and self-assembly dynamics driven by electrostatic interactions that occur on ultrafast timescales.

scholarly journals Stable and Metastable Phase Equilibria Involving the Cu6Sn5 Intermetallic

2021 ◽  
Author(s):  
A. Leineweber ◽  
M. Löffler ◽  
S. Martin
Keyword(s):  
Phase Equilibria ◽  
Electron Backscatter Diffraction ◽  
Metastable Phase ◽  
Stable Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Heat Treated ◽  
Ordered Phases ◽  
Backscatter Diffraction ◽  
Kinetics Of

Abstract Cu6Sn5 intermetallic occurs in the form of differently ordered phases η, η′ and η′′. In solder joints, this intermetallic can undergo changes in composition and the state of order without or while interacting with excess Cu and excess Sn in the system, potentially giving rise to detrimental changes in the mechanical properties of the solder. In order to study such processes in fundamental detail and to get more detailed information about the metastable and stable phase equilibria, model alloys consisting of Cu3Sn + Cu6Sn5 as well as Cu6Sn5 + Sn-rich melt were heat treated. Powder x-ray diffraction and scanning electron microscopy supplemented by electron backscatter diffraction were used to investigate the structural and microstructural changes. It was shown that Sn-poor η can increase its Sn content by Cu3Sn precipitation at grain boundaries or by uptake of Sn from the Sn-rich melt. From the kinetics of the former process at 513 K and the grain size of the η phase, we obtained an interdiffusion coefficient in η of (3 ± 1) × 10−16 m2 s−1. Comparison of this value with literature data implies that this value reflects pure volume (inter)diffusion, while Cu6Sn5 growth at low temperature is typically strongly influenced by grain-boundary diffusion. These investigations also confirm that η′′ forming below a composition-dependent transus temperature gradually enriches in Sn content, confirming that Sn-poor η′′ is metastable against decomposition into Cu3Sn and more Sn-rich η or (at lower temperatures) η′. Graphic Abstract

scholarly journals Kinetics of Network Formation and Heterogeneous Dynamics of an Egg White Gel Revealed by Coherent X-Ray Scattering

2021 ◽  
Vol 126 (9) ◽  
Author(s):  
Nafisa Begam ◽  
Anastasia Ragulskaya ◽  
Anita Girelli ◽  
Hendrik Rahmann ◽  
Sivasurender Chandran ◽  
...  
Keyword(s):  
Network Formation ◽  
Egg White ◽  
X Ray ◽  
X Ray Scattering ◽  
Heterogeneous Dynamics ◽  
Kinetics Of ◽  
Ray Scattering

Study on Adsorption of Crosslinked Starch Microspheres towards Heavy Metal Ions

2013 ◽  
Vol 834-836 ◽  
pp. 531-535
Author(s):  
Li Yan Yang ◽  
Yi Hui Guo ◽  
Li Li Yu ◽  
Jing You
Keyword(s):  
Metal Ions ◽  
Reversed Phase ◽  
Adsorption Rate ◽  
X Ray Diffraction ◽  
Adsorption Selectivity ◽  
X Ray ◽  
Starch Microsphere ◽  
Other Substances ◽  
Effects Of Media ◽  
Kinetics Of

A type of cross-linking starch microsphere (CSMs) has been synthesized via reversed phase suspension method. Crosslinked starch microsphere has good adsorption performance to metal ions in water. The adsorption kinetics of Co (II) on the CSMs, selectivity of adsorption CSMs towards Co (II),Cu (II),Pb (II),Cd (II) and adsorption effects of media towards Co (II) were investigated. The CSMs and its adsorption product were comparatively characterized by X-ray diffraction (XRD). The results showed that The adsorption rate is mainly controlled by liquid film diffusion, and the constant of adsorption rate is 0.0686min-1 at 308K. The crystal structure of the CSMs decreased greatly after the incorporation of Co (II). Co (II) has better adsorption selectivity on CSMs. Ions coexist and other substances in the solution have certain impact on adsorption. Those data are helpful for treatment of the wastewater containing heavy ions.

Efficient adsorption of chlorpyrifos onto modified activated carbon by gamma irradiation; a plausible adsorption mechanism

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Mohamed S. Yahia ◽  
Ahmed S. Elzaref ◽  
Magdy B. Awad ◽  
Ahmed M. Tony ◽  
Ahmed S. Elfeky
Keyword(s):  
Gamma Irradiation ◽  
Area Measurement ◽  
Maximum Adsorption Capacity ◽  
X Ray Diffraction ◽  
X Ray ◽  
First Order ◽  
Pseudo Second Order ◽  
Ft Ir ◽  
Pseudo First Order ◽  
Kinetics Of

Abstract Commercial Granulated Active Carbon (GAC) has been modified using 10 Gy dose Gamma irradiation (GAC10 Gy) for increasing its ability of air purification. Both, the raw and treated samples were applied for removing Chlorpyrifos pesticide (CPF) from ambient midair. Physicochemical properties of the two materials were characterized by Fourier Transform Infrared (FT-IR) and Raman spectroscopy. The phase formation and microstructure were monitored using X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), supported with Energy-Dispersive X-ray (EDX). The Surface area measurement was detected using BET particle size prosometry. Obtained outcomes showed that, the maximum adsorption capacity, given by Langmuir equations, was greatly increased from 172.712 to 272.480 mg/g for GAC and GAC10 Gy, respectively, with high selectivity. The overall removal efficiency of GAC10 Gy was notably comparable to that of the original GAC-sorbent. The present study indicated that, gamma irradiation could be a promising technique for treating GAC and turned it more active in eliminating the pesticides pollutants from surrounding air. The data of equilibrium has been analyzed by Langmuir and Freundlich models, that were considerably better suited for the investigated materials than other models. The process kinetics of CPF adsorbed onto both tested carbon versions were found to obey the pseudo first order at all concentrations with an exception at 70 mg/l using GAC, where, the spontaneous exothermic adsorption of Chlorpyrifos is a strong function for the pseudo-first order (PFO) and pseudo second order (PSO) kinetics.

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