scholarly journals Morphology of Barite Synthesized by In-Situ Mixing of Na2SO4 and BaCl2 Solutions at 200 °C

Crystals ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 962
Author(s):  
Chunyao Wang ◽  
Li Zhou ◽  
Shuai Zhang ◽  
Li Wang ◽  
Chunwan Wei ◽  
...  
Keyword(s):  
High Temperature ◽  
Hydrothermal Fluid ◽  
Room Temperature ◽  
Hydrothermal Systems ◽  
Dendritic Morphology ◽  
New Method ◽  
Precipitation Mechanism ◽  
Factors Affecting

Barite is an abundant sulfate mineral in nature. Especially, the variety of morphologies of barite is often driven by the mixing of Ba-bearing hydrothermal fluid and sulfate-bearing seawater around hydrothermal chimneys. In order to better understand the factors affecting the morphology and precipitation mechanism(s) of barite in seafloor hydrothermal systems, we synthesized barite by a new method of in-situ mixing of BaCl2 and Na2SO4 solutions at 200 °C while varying Ba concentrations and ratios of Ba2+/SO42−, and at room temperature for comparison. The results show that barite synthesized by in-situ mixing of BaCl2 and Na2SO4 solutions at 200 °C forms a variety of morphologies, including rod-shaped, granular, plate-shaped, dendritic, X-shaped, and T-shaped morphologies, while room temperature barites display relatively simple, granular, or leaf-like morphologies. Thus, temperature affects barite morphology. Moreover, dendritic barite crystals only occurred at conditions where Ba2+ is in excess of SO42− at the experimental concentrations. The dendritic morphology of barite may be an important typomorphic feature of barite formed in high-temperature fluids directly mixing with excess Ba2+ relative to SO42−.

A Novel and Efficient Alkoxylselenenylation of Alkenes

2019 ◽  
Vol 41 (6) ◽  
pp. 1039-1039
Author(s):  
Yingguo Fang and Jie Yan Yingguo Fang and Jie Yan
Keyword(s):  
Room Temperature ◽  
Electrophilic Addition ◽  
New Method ◽  
Reaction Conditions ◽  
Selenium Species

A novel and efficient alkoxylselenenylation from alkenes, diselenides, and alcohols mediated by iodine is developed, with which a series of β-alkoxy selenides are synthesized. In this procedure, firstly, I2 reacts with diselenide to form in situ the active electrophilic selenium species RSeI, then following an electrophilic addition of it to alkenes provides β-alkoxy selenides with high regioselectivity and in good yields. This new method for achieving β-alkoxy selenides has some advantages over other methods such as using available and cheap iodine as the oxidizing species at room temperature, which makes this reaction has milder reaction conditions and simpler procedure.

Analyses of Eutectoid Phase Transformations in Nb–SilicideIn SituComposites

2004 ◽  
Vol 10 (4) ◽  
pp. 470-480 ◽  
Author(s):  
B.P. Bewlay ◽  
S.D. Sitzman ◽  
L.N. Brewer ◽  
M.R. Jackson
Keyword(s):  
Crystal Structure ◽  
Phase Transformation ◽  
High Temperature ◽  
Room Temperature ◽  
Bulk Composition ◽  
High Strength ◽  
Eutectoid Decomposition ◽  
Quaternary Alloys ◽  
Temperature Fracture

Nb–silicide in situ composites have great potential for high-temperature turbine applications. Nb–silicide composites consist of a ductile Nb-based solid solution together with high-strength silicides, such as Nb5Si3and Nb3Si. With the appropriate addition of alloying elements, such as Ti, Hf, Cr, and Al, it is possible to achieve a promising balance of room-temperature fracture toughness, high-temperature creep performance, and oxidation resistance. In Nb–silicide composites generated from metal-rich binary Nb-Si alloys, Nb3Si is unstable and experiences eutectoid decomposition to Nb and Nb5Si3. At high Ti concentrations, Nb3Si is stabilized to room temperature, and the eutectoid decomposition is suppressed. However, the effect of both Ti and Hf additions in quaternary alloys has not been investigated previously. The present article describes the discovery of a low-temperature eutectoid phase transformation during which (Nb)3Si decomposes into (Nb) and (Nb)5Si3, where the (Nb)5Si3possesses the hP16 crystal structure, as opposed to the tI32 crystal structure observed in binary Nb5Si3. The Ti and Hf concentrations were adjusted over the ranges of 21 to 33 (at.%) and 7.5 to 33 (at.%) to understand the effect of bulk composition on the phases present and the eutectoid phase transformation.

scholarly journals Improvement of High Temperature Wear Behavior of In-Situ Cr3C2-20 wt. % Ni Cermet by Adding Mo

Crystals ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. 682
Author(s):  
Liang Sun ◽  
Wenyan Zhai ◽  
Hui Dong ◽  
Yiran Wang ◽  
Lin He
Keyword(s):  
Wear Resistance ◽  
High Temperature ◽  
Wear Mechanism ◽  
Room Temperature ◽  
Wear Behavior ◽  
Ceramic Particle ◽  
High Temperature Wear ◽  
The Coefficient Of Friction ◽  
Mo Content

Cr3C2-Ni cermet is a kind of promising material especially for wear applications due to its excellent wear resistance. However, researches were mainly concentrated on the experiment condition of room temperature, besides high-temperature wear mechanism of the cermet would be utilized much potential applications and also lack of consideration. In present paper, the influence of Mo content on the high-temperature wear behavior of in-situ Cr3C2-20 wt. % Ni cermet was investigated systematically. The friction-wear experiment was carried out range from room temperature to 800 °C, while Al2O3 ceramic was set as the counterpart. According to experimental results, it is indicated that the coefficient of friction (COF) of friction pairs risen at the beginning of friction stage and then declined to constant, while the wear rate of Cr3C2-20 wt. % Ni cermet risen continuously along with temperature increased, which attributes to the converted wear mechanism generally from typical abrasive wear to severe oxidation and adhesive wear. Generally, the result of wear resistance was enhanced for 13.4% (at 400 °C) and 31.5% (at 800 °C) by adding 1 wt. % Mo. The in-situ newly formed (Cr, Mo)7C3 ceramic particle and the lubrication phase of MoO3 can effectively improve the wear resistance of Cr3C2-20 wt. % Ni cermet.

scholarly journals The High-Temperature Transformation from 1T- to 3R-LixTiS2 (x = 0.7, 0.9) as Observed in situ with Neutron Powder Diffraction

2015 ◽  
Vol 229 (9) ◽  
Author(s):  
Dennis Wiedemann ◽  
Suliman Nakhal ◽  
Anatoliy Senyshyn ◽  
Thomas Bredow ◽  
Martin Lerch
Keyword(s):  
High Temperature ◽  
Powder Diffraction ◽  
Electrode Material ◽  
Room Temperature ◽  
Lithium Ion ◽  
Neutron Powder Diffraction ◽  
Titanium Disulfide ◽  
Temperature Transformation

AbstractLayered titanium disulfide is used as lithium-ion intercalating electrode material in batteries. The room-temperature stable trigonal 1T polymorphs of the intercalates Li

Synchroshear Versus Conventional Shear Mechanisms in Transitionmetal Disilicides with the C40 Structure

1999 ◽  
Vol 578 ◽  
Author(s):  
H. Inui ◽  
M. Yamaguchi
Keyword(s):  
High Temperature ◽  
Low Temperature ◽  
Plastic Flow ◽  
Deformation Mechanism ◽  
Deformation Behavior ◽  
Basal Slip ◽  
Room Temperature ◽  
Onset Temperature ◽  
Factors Affecting ◽  
Temperature Group

AbstractThe deformation behavior of (0001) <1210> basal slip in single crystals of five different transitionmetal disilicides with the C40 structure has been investigated in the temperature range from room temperature to 1500°C in compression. These disilicides are found to be classified into two groups depending on the onset temperature for plastic flow. The low-temperature group, which consists of VSi2, NbSi2 and TaSi2, exhibits the onset temperature for plastic flow around 0.3 T/Tm (melting temperature) and deforms by a conventional shear mechanism. In contrast, the high temperature group, which consists of CrSi2 and Mo(Si,Al)2, exhibits the onset temperature around 0.6T/Tm and deforms by a synchroshear mechanism. Factors affecting the deformation mechanism in these C40 disilicides are discussed in terms of directionality of atomic bonding and the relative stability of the C40 phase with respect to the C11b phase.

Microstructure and microtexture of a Nb-16%Si (DS) Alloy

1995 ◽  
Vol 53 ◽  
pp. 122-123
Author(s):  
J. A. Sutliff ◽  
B. P. Bewlay
Keyword(s):  
High Temperature ◽  
Directional Solidification ◽  
Room Temperature ◽  
Microstructural Characterization ◽  
Crystallographic Analysis ◽  
Directionally Solidified ◽  
Heat Treated ◽  
Other Orientation

In-situ composite Nb-Si alloys have been studied by several investigators as potential high temperature structural materials. The two major processing routes used to fabricate these composites are directional solidification and extrusion of arc-cast solidified ingots. In both cases a stable microstructure of primary Nb dendrites in a eutectoid of Nb and Nb5Si3 phases is developed after heat treatment. The Nb5Si3 phase is stable at room temperature and forms as a decomposition product of the high temperature Nb3Si phase. The anisotropic microstructures developed by both directional solidification and extrusion require evaluation of the texture to fully interpret the fracture and other orientation dependent mechanical behavior of these composites.In this paper we report on the microstructural characterization of a directionally solidified (DS) and heat treated Nb-16 at.%Si alloy. The microtexture of each of the phases (Nb, Nb5Si3) was determined using the Electron BackScattering Pattern (EBSP) technique for electron diffraction in the scanning electron microscope. A system employing automatic diffraction pattern recognition, crystallographic analysis, and sample or beam scanning was used to acquire the microtexture data.

scholarly journals High-Temperature Tribological Performance of Hard Multilayer TiN-AlTiN/nACo-CrN/AlCrN-AlCrO-AlTiCrN Coating Deposited on WC-Co Substrate

Coatings ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 909 ◽  
Author(s):  
Asad Alamgir ◽  
Maxim Yashin ◽  
Andrei Bogatov ◽  
Mart Viljus ◽  
Rainer Traksmaa ◽  
...  
Keyword(s):  
High Temperature ◽  
Room Temperature ◽  
Energy Dispersive Spectrometry ◽  
X Ray Diffraction ◽  
X Ray ◽  
Mechanical And Tribological Properties ◽  
Diamond Indenter ◽  
Scratch Tests ◽  
Ball On Disc

Mechanical and tribological properties of the hard-multilayer TiN-AlTiN/nACo-CrN/AlCrN-AlCrO-AlTiCrN coating deposited on WC-Co substrate were investigated. The sliding tests were carried out using ball-on-disc tribometer at room (25 °C) and high temperatures (600 and 800 °C) with Al2O3 balls as counterpart. Nano-scratch tests were performed at room temperature with a sphero-conical diamond indenter. The surface morphology and chemical composition were investigated with scanning electron microscopy (SEM), energy-dispersive spectrometry (EDS) and in-situ high-temperature X-ray diffraction (HT-XRD). The phase transition from fcc-(Al,Cr)2O3 into α-(Al,Cr)2O3 was observed at about 800 °C. The results of the tribological tests depends on the temperature, the lowest apparent and real wear volumes were observed on the coating after the test at 800 °C along with the smallest coefficient of friction (COF). The plastic deformation of the coating was confirmed in sliding and nano-scratch tests. The nano-scratch tests revealed the dependence of COF value on the temperature of the sliding tests.

EBSD Coupled to SEM In Situ Annealing as a Tool to Identify Recrystallization Mechanisms - Application to Zr and Ta Alloys

2012 ◽  
Vol 715-716 ◽  
pp. 486-491
Author(s):  
Nathalie Bozzolo ◽  
S. Jacomet ◽  
M. Houillon ◽  
B. Gaudout ◽  
Roland E. Logé
Keyword(s):  
High Temperature ◽  
Short Duration ◽  
Microstructure Evolution ◽  
Room Temperature ◽  
Heat Treatments ◽  
Cooling Rates ◽  
Heating And Cooling ◽  
Orientation Mapping ◽  
High Heating

A heating stage as been developed to perform in-situ annealing in a SEM equipped with an EBSD system in order to study recrystallization mechanisms. High temperature treatments could then be performed inside the SEM, up to 1180°C and with high heating-and cooling-rates (~100°C.s-1). Samples were cooled down to room temperature to perform EBSD orientation mapping in between successive short-duration heat-treatments. Microstructure evolution snapshots obtained this way are presented in this paper to show recrystallization in Zircaloy4 and in pure tantalum.

scholarly journals Phase transition and atomic structure of Cd6Tb 1/1 approximant to quasicrystal

2014 ◽  
Vol 70 (a1) ◽  
pp. C95-C95
Author(s):  
Dan Liu ◽  
Tsunetomo Yamada ◽  
Cesar Gómez ◽  
Vaclav Petricek ◽  
Michal Dusek ◽  
...  
Keyword(s):  
Phase Transition ◽  
High Temperature ◽  
Atomic Structure ◽  
Room Temperature ◽  
Structural Phase ◽  
Icosahedral Quasicrystal ◽  
Temperature Phase ◽  
Temperature Structure ◽  
Antiferromagnetic Ordering

We present an in-situ temperature study of the atomic structure of the 1/1 Cd6Tb approximant to an icosahedral quasicrystal. It belongs to the `Tsai' type family of quasicrystal and approximants whose archetype is the well-studied Cd-Yb system[1]. Its high temperature structure can be described as a bcc packing of a large Tsai atomic cluster, whose inner shell is a disordered tetrahedron at room temperature. As for most of the Cd6RE (RE=rare earth) approximant, the Cd6Tb phase undergoes a phase transition at 190 K to a phase of lower symmetry, resulting from an ordering of the inner tetrahedron[2]. Moreover, it has been shown that this phase undergoes a magnetic phase transition below 20 K, with an antiferromagnetic ordering of the Tb moment bearing atoms. It is thus particularly important to have a detailed structural study of this phase. We have carried out a systematic in situ measurement on a single grain from room temperature down to 40K on the crystal beam line located at the Soleil synchrotron. The structural phase transition is observed at about 190K. Using different attenuation, we have collected integrated intensity in a large dynamical range, leading to more than 60000 unique reflections in the C2/c monoclinic low temperature phase. The final wR2 values for room temperature and 40K are equal to 0.0726 and 0.0905 respectively. The resulting atomic structure will be compared to the well-studied approximant Zn6Sc, which is isostructural to Cd6Tb[3]. The ordering of the innermost tetrahedron leads to the distortion of the successive shells. The evolution of the high temperature phase, in particular just above Tc where pretransitional diffuse scattering is observed will be presented.

Sign in / Sign up

Export Citation Format

Share Document