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.

Eco-Friendly Synthesis and Applicability to Silver Ink of Silver Nanoparticles Prepared via Stepwise-Modified Tollens Method

2021 ◽  
Vol 21 (4) ◽  
pp. 2568-2575
Author(s):  
Nguyen Cong Tu ◽  
Ho Minh Sang ◽  
Luu Thi Lan Anh ◽  
Nguyen Huu Lam
Keyword(s):  
Silver Nanoparticles ◽  
Acetic Acid ◽  
Citric Acid ◽  
Acid Solution ◽  
Room Temperature ◽  
X Ray Diffraction ◽  
Silver Ink ◽  
Stepwise Method ◽  
Mean Size ◽  
The Mean

Silver nanoparticles were eco-friendly synthesized at room temperature via a Tollens process modified with the stepwise method using eco-friendly precursors (citric acid and acetic acid). The field emission scanning electron spectroscopy was used to study the morphology of silver nanoparticles. The mean size of silver nanoparticles and the components of products were theoretically determined using UV-Vis and X-ray Diffraction spectra. The mole ratio between the silver ion, citric acid and the buffer acid solution (acetic acid) strongly influences the mean size and the composition of the product. The appearance of acetic acid in the buffer acid solution helped increase the efficiency of silver nanoparticles preparation. With the mole ratio n[Ag+]:ncitric:nacetic = 1.0:2.5:2.5, the highest preparation efficiency was obtained, the silver nanoparticles had an average dimension of ˜11 nm and narrow size distribution. The silver nanoparticles were dispersed into different solvents to examine their applicability to silver ink. The silver ink using propylene glycol solvent showed good applicability to silver ink which could work at room temperature.

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.

Microstructure Evolution of AZ31 Magnesium Alloy during Warm Compression Forming

2007 ◽  
Vol 539-543 ◽  
pp. 1813-1817
Author(s):  
Zhi Min Zhang ◽  
Qiang Wang ◽  
B.C. Li ◽  
X. Zhang
Keyword(s):  
Microstructural Evolution ◽  
Room Temperature ◽  
Effective Strain ◽  
Mg Alloy ◽  
Compression Tests ◽  
Az31 Mg Alloy ◽  
Microstructural Evaluation ◽  
Mean Size ◽  
The Mean ◽  
Different Thickness

Warm compression tests of AZ31 Mg alloy were carried out at five temperatures in 30°C intervals from 210°C to 330°C. The samples of different thickness which were machined from as-cast and pre-strained AZ31 billets were compressed into thickness 1mm and then cooled in the air to room temperature. The microstructural evolution of AZ31 Mg alloy was investigated during warm compression forming. The results show that all the samples have undergone a microstructure changes to different scales in the range investigated. The twinning is the predominant deformation mechanism for magnesium alloys at moderate temperatures and its occurrence is dependent on temperature and strain. Microstructural evaluation indicates that the mean size of the recrystallised grains decreases with increasing effective strain and temperature because of sufficient dynamic recrystallization. The original grain has significant influence on microstructural evolution during warm forming.

Preparation of Plate-Like Bulk Beta Iron-Disilicide Crystals Using Metal to Semiconductor Phase Transition by Heat Treatment

2002 ◽  
Vol 749 ◽  
Author(s):  
Masato Osamura ◽  
Hidetaka Ishihara ◽  
Zhengxin Liu ◽  
Hisao Tanoue ◽  
Shirou. Sakuragi ◽  
...  
Keyword(s):  
Chemical Vapor ◽  
Chemical Vapor Transport ◽  
Annealing Duration ◽  
Bulk Crystals ◽  
X Ray Diffraction ◽  
X Ray ◽  
Flat Surfaces ◽  
The Matrix ◽  
The Mean ◽  
Micro Analysis

ABSTRACTPlate-like β-FeSi2 bulk crystals with size of 10×10 mm2 and thickness of 1 mm were fabricated by annealing CVT (chemical vapor transport)-grown plate-like α-Fe2Si5 at 800°C in Ar atmosphere. Before annealing, α-Fe2Si5 crystals were characterized by x-ray diffraction (XRD) and scanning electron microscopy (SEM) to be single crystals with flat surfaces. XRD measurements of β-FeSi2 crystals subjected to annealing showed that they had a po lycrystalline structure. The mean Fe/Si co mposit ion rat io of β-FeSi2 crystal measured by energy dispersive x-ray spectroscopy (EDX) was 31/69 and it was the same as that of α-Fe2Si5 bulk crystal before annealing. SEM, Raman scattering and electron probe micro-analysis (EPMA) measurements identified that there existed small Si precipitates mixed in the matrix of β-FeSi2 crystals. At annealing temperature of 800°C, the plate-like β-FeSi2 bulk was obtained even the annealing duration time was as short as 5 hours.

INDIRECT MEASUREMENT OF Zn-DOPED In2S3 NANOFILMS' SPECIFIC HEAT CAPACITY

2008 ◽  
Vol 07 (04n05) ◽  
pp. 229-233 ◽  
Author(s):  
S. LAZZEZ ◽  
K. BOUBAKER BEN MAHMOUD ◽  
M. AMLOUK
Keyword(s):  
Heat Capacity ◽  
Electron Microscope ◽  
Specific Heat ◽  
Specific Heat Capacity ◽  
Room Temperature ◽  
Thermal Analyses ◽  
Indirect Measurement ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
The Mean

ZnIn 2 S 4 nanofilms were grown on In 2 S 3 substrates. The band gap of ZnIn 2 S 4 barriers was approximately 2.8 eV at room temperature. The morphology and structure of the obtained nanofilms were already investigated via transmission electron microscope (TEM), scanning electron microscope (SEM) and X-ray diffraction analyses.1,2 In this paper, thermal analyses are performed via a photothermal technique, which has been used to indirectly evaluate the specific heat capacity of the obtained Zn -doped nanofilms. The yielded value for an optimal zinc-to-indium ratio, x (0.33), at the mean room temperature (T∞ = 301 K ), was Cs ≈ 411.5 J K -1 kg -1.

Macro-and Microstrain Relaxation in Annealed Ag Films During Ageing at Room Temperature

1997 ◽  
Vol 505 ◽  
Author(s):  
R. C. Currie ◽  
R. Delhez ◽  
E. J. Mitiemeijer
Keyword(s):  
Room Temperature ◽  
Strain Relaxation ◽  
Diffraction Line ◽  
Line Broadening ◽  
X Ray Diffraction ◽  
Thermally Induced ◽  
X Ray ◽  
Diffraction Line Profile ◽  
The Matrix ◽  
Profile Position

ABSTRACTThe relaxation of thermally induced strain in 500 nm thick polycrystalline Ag layers electron-beam deposited onto Si wafers was traced during ageing at room temperature. The layers consisted predominantly of matrix crystallites with {111} planes parallel to the surface and twin crystallites with {51 l} planes parallel to the surface. The macrostrain in the plane of the layer was determined from the X-ray diffraction line-profile position and the microstrain from the diffraction-line broadening. The residual macrostress relaxed from 160 MPa to 30 MPa in the matrix crystallites and from 170 MPa to 50 MPa in the twin crystallites. Simultaneously with the decrease in macrostress the microstrain decreases significantly for both texture fractions. The strain relaxation behaviour is governed by movement and subsequent annihilation of defects in the layer.

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.

Investigation on Microstructure and Phase Transformation of La Added Ti49.3Ni50.7 Shape Memory Alloy

2012 ◽  
Vol 557-559 ◽  
pp. 1041-1044 ◽  
Author(s):  
Jia Wen Xu ◽  
Ai Lian Liu ◽  
Bing Yu Qian ◽  
Wei Cai
Keyword(s):  
Phase Transformation ◽  
Room Temperature ◽  
Optical Microscope ◽  
X Ray Diffraction ◽  
Transformation Behavior ◽  
Phase Transformation Behavior ◽  
Ni Alloys ◽  
Ni Alloy ◽  
The Matrix ◽  
La Addition

The effect of La addition on the microstructure and phase transformation behavior of Ti 49.3Ni50.7 alloy is investigated by optical microscope (OP), scanning electron microscope (SEM), X-ray diffraction analysis (XRD) and differential scanning calorimeter (DSC). The results show that the microstructure of Ti-Ni alloy is changed obviously with La addition, and the microstructure of Ti-Ni alloy containing La at room temperature is made up of the matrix and LaNi phase. La addition firstly increases the martensitic transformation temperatures evidently and the increase of Ms is about 62°C with 1at.% La. Secondly Adding La changes the type of phase transformation behavior of Ti-Ni alloys, and R phase transformation with Rs temperature about room temperature occurs in La added Ti-Ni alloy.

scholarly journals Investigation of Y2.1Er0.9(ScxGa1−x)5O12 Matrix Components on the Spectral Properties around 3.0 μm by Micro-Pulling-Down Method

Crystals ◽  
2019 ◽  
Vol 9 (3) ◽  
pp. 138
Author(s):  
Zhijiang Che ◽  
Jian Zhang ◽  
Baiyi Wu ◽  
Qiangqiang Hu ◽  
Wenxiang Mu ◽  
...  
Keyword(s):  
Fluorescence Spectra ◽  
Room Temperature ◽  
Lattice Vibration ◽  
Emission Spectra ◽  
X Ray Diffraction ◽  
Mid Infrared ◽  
X Ray ◽  
Electron Probe Microanalyzer ◽  
The Matrix ◽  
Crystal Fibers

Single crystal fibers of 30% Er3+-doped compound of Y3(ScxGa1−x)5O12 have been grown by using the micro-pulling down (μ-PD) technique successfully. Our main purpose is to tune the fluorescence properties by adjusting the ratios of Sc3+ and Ga3+ ions inside the matrix crystals. The crystal structures of the series compounds were measured and analyzed through X-ray diffraction (XRD) measurements. The components and doping elements distributions were measured by the X-ray Fluorescence spectrometry and electron-probe microanalyzer. The absorption and mid-infrared fluorescence spectra, including the fluorescent lifetime of Er3+:4I13/2 and 4I11/2 levels were measured and compared systematically at room temperature. Spectral analysis indicated that the fluorescent lifetime of Er3+:4I13/2 tended to shorten and the emission spectra began to show a red shift when the proportion of YSG increased in the compound. Furthermore, the Raman spectra were measured to reveal the variations of lattice vibration and phonon energy.

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