scholarly journals Mudrock Microstructure: A Technique for Distinguishing between Deep-Water Fine-Grained Sediments

Minerals ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 653
Author(s):  
Shereef Bankole ◽  
Dorrik Stow ◽  
Zeinab Smillie ◽  
Jim Buckman ◽  
Helen Lever
Keyword(s):  
Grain Size ◽  
Deep Water ◽  
Sedimentary Facies ◽  
X Ray Diffraction ◽  
Weak Current ◽  
Large Area ◽  
Fine Grained ◽  
Mean Size ◽  
The Mean ◽  
Water Facies

Distinguishing among deep-water sedimentary facies has been a difficult task. This is possibly due to the process continuum in deep water, in which sediments occur in complex associations. The lack of definite sedimentological features among the different facies between hemipelagites and contourites presented a great challenge. In this study, we present detailed mudrock characteristics of the three main deep-water facies based on sedimentological characteristics, laser diffraction granulometry, high-resolution, large area scanning electron microscopy (SEM), and the synchrotron X-ray diffraction technique. Our results show that the deep-water microstructure is mainly process controlled, and that the controlling factor on their grain size is much more complex than previously envisaged. Retarding current velocity, as well as the lower carrying capacity of the current, has an impact on the mean size and sorting for the contourite and turbidite facies, whereas hemipelagite grain size is impacted by the natural heterogeneity of the system caused by bioturbation. Based on the microfabric analysis, there is a disparate pattern observed among the sedimentary facies; turbidites are generally bedding parallel due to strong currents resulting in shear flow, contourites are random to semi-random as they are impacted by a weak current, while hemipelagites are random to oblique since they are impacted by bioturbation.

scholarly journals Preparation of high-entropy carbides by different sintering techniques

2021 ◽  
Vol 56 (19) ◽  
pp. 11237-11247 ◽  
Author(s):  
Johannes Pötschke ◽  
Manisha Dahal ◽  
Mathias Herrmann ◽  
Anne Vornberger ◽  
Björn Matthey ◽  
...  
Keyword(s):  
Grain Size ◽  
Single Phase ◽  
X Ray Diffraction ◽  
Vacuum Sintering ◽  
X Ray ◽  
High Entropy ◽  
Mean Grain Size ◽  
The Mean ◽  
Gas Pressure Sintering ◽  
Hardness Values

AbstractDense (Hf, Ta, Nb, Ti, V)C- and (Ta, Nb, Ti, V, W)C-based high-entropy carbides (HEC) were produced by three different sintering techniques: gas pressure sintering/sinter–HIP at 1900 °C and 100 bar Ar, vacuum sintering at 2250 °C and 0.001 bar as well as SPS/FAST at 2000 °C and 60 MPa pressure. The relative density varied from 97.9 to 100%, with SPS producing 100% dense samples with both compositions. Grain size measurements showed that the substitution of Hf with W leads to an increase in the mean grain size of 5–10 times the size of the (Hf, Ta, Nb, Ti, V,)C samples. Vacuum-sintered samples showed uniform grain size distribution regardless of composition. EDS mapping revealed the formation of a solid solution with no intermetallic phases or element clustering. X-ray diffraction analysis showed the structure of mostly single-phase cubic high-entropy carbides. Hardness measurements revealed that (Hf, Ta, Nb, Ti, V)C samples possess higher hardness values than (Ta, Nb, Ti, V, W)C samples.

Lead inclusions in aluminium

1989 ◽  
Vol 157 ◽  
Author(s):  
E. Johnson ◽  
L. Gråbaek ◽  
J. Bohr ◽  
A. Johansen ◽  
L. Sarholt-Kristensen ◽  
...  
Keyword(s):  
Hysteresis Loop ◽  
Room Temperature ◽  
Noble Gas ◽  
Melting Transition ◽  
X Ray Diffraction ◽  
Free Surfaces ◽  
The Matrix ◽  
Mean Size ◽  
The Mean ◽  
Spontaneous Phase

ABSTRACTIon implantation at room temperature of lead into aluminium leads to spontaneous phase separation and formation of lead precipitates growing topotactically with the matrix. Unlike the highly pressurised (∼ 1–5 GPa) solid inclusions formed after noble gas implantations, the pressure in the lead precipitates is found to be less than 0.12 GPa.Recently we have observed the intriguing result that the lead inclusions in aluminium exhibit both superheating and supercooling [1]. In this paper we review and elaborate on these results. Small implantation-induced lead precipitates embedded in an aluminium matrix were studied by X-ray diffraction. The (111) Bragg peak originating from the lead crystals was followed during several temperature cycles, from room temperature to 678 K. The melting temperature for bulk lead is 601 K. In the first heating cycle we found a superheating of the lead precipitates of 67 K before melting occurred. During subsequent cooling a supercooling of 21 K below the solidification point of bulk lead was observed. In the subsequent heating cycles this hysteresis at the melting transition was reproducible. The full width of the hysteresis loop slowly decreased to 62 K, while the mean size of the inclusions gradually increased from 14.5 nm to 27 nm. The phenomena of superheating and supercooling are thus most pronounced for the small crystallites. The persistence of the hysteresis loop over successive heating cycles demonstrate that its cause is intrinsic in nature, and it is believed that the superheating originates from the lack of free surfaces of the lead inclusions.

Synthesis and Characterization of Plasma Synthesized Nanostructured Magnesia-Yttria Based Nanocomposites

2007 ◽  
Vol 1056 ◽  
Author(s):  
Jafar F. Al-Sharab ◽  
Rajendra Sadangi ◽  
Vijay Shukla ◽  
Bernard Kear
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Grain Size ◽  
Chemical Mapping ◽  
X Ray Diffraction ◽  
Fine Grained ◽  
Transmission Electron ◽  
Spray Method ◽  
Average Grain Size

ABSTRACTPolycrystalline Y2O3 is the material of choice for IR windows since it has excellent optical properties in the visible, and near infra-red band. However, current processing methods yield polycrystalline Y2O3 with large grain size (> 100 μm), which limits the hardness and erosion resistance attainable. One way to improve strength is to develop an ultra-fine grained material with acceptable optical transmission properties. To realize a fine-grained ceramic, one approach is to develop a composite structure, in which one phase inhibits the growth of the other phase during processing. In this study, Y2O3-MgO nanocomposite with various MgO content (20, 50 and 80 mol%) were synthesized using plasma spray method. Extensive characterization techniques including x-ray diffraction, scanning electron microscopy (SEM), Transmission electron microscopy (TEM) and Energy Dispersive spectrometry (EDS) were employed to study the synthesized powder as well as the consolidated sample. Transmission Electron Microscopy, as well as EDS chemical mapping, revealed that the consolidated sample have bi-continuous MgO-Y2O3 nanostructure with an average grain size of 200 nm.

Mechanical Properties of Porous Nanophase Materials Measured by Instrumental Indentation

1995 ◽  
Vol 400 ◽  
Author(s):  
H. Van Swygenhoven ◽  
W. Wagner ◽  
J. Löffler
Keyword(s):  
Mechanical Properties ◽  
Grain Size ◽  
Annealing Temperature ◽  
X Ray Diffraction ◽  
X Ray ◽  
Gas Condensation ◽  
Mean Grain Size ◽  
Nanophase Materials ◽  
The Mean ◽  
Instrumental Indentation

AbstractMechanical properties of nanostructured intermetallic Ni3Al synthesized by the inert-gas condensation technique are studied by means of instrumental indentation using the ICT-CSEMEX indenter. This instrument is a microindenter which continously measures load and displacement. Load-displacement curves are performed as function of grain size, consolidation- and annealing temperature. The mean grain size of the samples are studied by means of x-ray diffraction and small-angle neutron scattering.

Surface Modification and Preparation of High Purity Nanometer Magnesium Hydroxide Using Impinging Stream

2011 ◽  
Vol 675-677 ◽  
pp. 847-851
Author(s):  
Jian Hai Zhao ◽  
Yan Ping Lai
Keyword(s):  
Surface Modification ◽  
Magnesium Hydroxide ◽  
High Purity ◽  
X Ray Diffraction ◽  
Control Factors ◽  
Operation Conditions ◽  
Crystallization Method ◽  
Transmission Electron ◽  
Mean Size ◽  
The Mean

High purity nanometer magnesium hydroxide is produced by impinging stream reaction crystallization method using bischofite as feedstock. Effects of operation conditions on the impinging stream of Mg (OH)2 are reported and the control factors of purity are confirmed. The morphology of the powder was characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). Result shows that purity of Mg (OH)2 can reach 99% and the mean size of crystal is 13.5nm. Surface modification of nano-sized magnesium hydroxide using four surface modifiers such as sodium steatite, sodium laurylsulfonate, sodium oleate and sodium silicate were investigated in this paper. The modified magnesium hydroxide has smaller particle size, larger powder contact angle, slower sedimentation velocity, the less in-oil capacity than unmodified sample

Synthesis and Characterization of Surface Protected Nanocrystalline Particles of Titania

1998 ◽  
Vol 519 ◽  
Author(s):  
E. Scolan ◽  
C. Sanchez
Keyword(s):  
X Ray Diffraction ◽  
Elastic Light Scattering ◽  
Titanium Butoxide ◽  
X Ray ◽  
Toluene Sulfonic Acid ◽  
Nanocrystalline Particles ◽  
Mean Size ◽  
The Mean ◽  
Cp Mas Nmr

AbstractMonodisperse non-aggregated nanoparticles of titania are obtained through hydrolysis at 60°C of titanium butoxide in the presence of acetylacetone and para-toluene sulfonic acid. After drying the resulting xerosols can be dispersed without aggregation in water-alcoholic or alcoholic solutions. The characterizations of the nanoparticles have been carried out by using quasi-elastic light scattering (QELS), 13C 1H in solution and X-ray diffraction, TEM, TG-DTA, 13C CP-MAS NMR in the solid state. The mean size of the anatase oxide core can be adjusted in the I to 5 nanometer range by a careful tuning of the synthetic conditions. The anatase particles are surrounded by acetylacetonato ligands, para-toluene sulfonate based species and water.

Characterization of Ultra Fine Palladium Particles with the Mean Size of 20 A by X-Ray Diffraction

1981 ◽  
Vol 50 (9) ◽  
pp. 3071-3074 ◽  
Author(s):  
Ken-ichi Ohshima ◽  
Shigeki Yatsuya ◽  
Jimpei Harada
Keyword(s):  
X Ray Diffraction ◽  
X Ray ◽  
Mean Size ◽  
The Mean ◽  
Palladium Particles

The Distribution of Bottom Sediments in Loch Leven, Kinross

1974 ◽  
Vol 74 ◽  
pp. 69-80 ◽  
Author(s):  
S. E. Calvert
Keyword(s):  
Grain Size ◽  
Organic Carbon ◽  
Deep Water ◽  
General Distribution ◽  
Sediment Type ◽  
Fine Grained ◽  
The North ◽  
Loch Leven ◽  
Highly Correlated ◽  
Deep Area

SynopsisThe sediments of shallow and deep water areas of Loch Leven are, respectively, medium to very fine-grained sands and silty clays (muds). The largest area of more or less uniform sediment type (sands) occurs on the north-eastern shelf. The sediments with the finest grain size are found in an area to the south and east of Castle Island and Reed Bower. Here, the median grain size is less than 4 microns. The amount of sand in a sediment is very highly correlated with the median grain size of the sediment and may therefore most usefully be used to describe the general distribution of sediments in the loch. The distribution of organic carbon in the loch sediments is largely confined to deep-water areas. The southern deep area is more organic rich than the northern deep area. The amount of organic carbon in a sediment is positively correlated with the amounts of clay and silt in the sediment.

Preparation of hexagonal cerium oxide nanoflakes by a surfactant-free route and its optical property

2007 ◽  
Vol 22 (11) ◽  
pp. 3006-3013 ◽  
Author(s):  
X. Yu ◽  
P. Ye ◽  
L. Yang ◽  
S. Yang ◽  
P. Zhou ◽  
...  
Keyword(s):  
Cerium Oxide ◽  
Visible Region ◽  
Blue Shift ◽  
Emission Peak ◽  
X Ray Diffraction ◽  
X Ray ◽  
Strong Reflection ◽  
Mean Size ◽  
The Mean ◽  
Pl Emission

Hexagonal cerium oxide nanoflakes have been synthesized by using a surfactant-free route. Transmission electcron microscopy (TEM), x-ray diffraction (XRD), infrared spectroscopy (FTIR), thermogravimetric and differential thermal analysis (TG-DTA), Brunauer–Emmett–Teller adsorption isotherm (BET), photoluminescence (PL), and ultraviolet–visible (UV–VIS) were used to characterize the sample. The mean size of the nanoflakes is about 30 nm and the specific surface is about 70.08 m2·g−1 when annealed at 400 °C. The acidity and superfluous NH4NO3 play a key role on the formation of nanoflakes in which there exists Ce (IV) and very little Ce (III). The nanoflakes exhibit a wide PL emission peak among 350–400 nm, strong absorption ranged from 200–450 nm, and strong reflection in the visible region. As the sizes of as-prepared samples decrease, a clear blue shift in the absorbing edge is observed. The linear relationship between ΔEg and D is shown in a log–log plot. The as-prepared cerium oxide nanoflakes can be widely used as UV absorbent and polishing materials.

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