scholarly journals Elemental Distribution in Individual Rain Droplets Determined by a Combination of the Replication Method and the Synchrotoron Radiation X-ray Fluorescence Microprobe Technique

2006 ◽  
Vol 22 (3) ◽  
pp. 415-419 ◽  
Author(s):  
Chang-Jin MA ◽  
Susumu TOHNO ◽  
Mikio KASAHARA ◽  
Shinjiro HAYAKAWA
Keyword(s):  
Elemental Distribution ◽  
X Ray ◽  
Replication Method ◽  
Microprobe Technique

X-Ray absorption edge elemental imaging of B. thuringienis

1989 ◽  
Vol 47 ◽  
pp. 212-213
Author(s):  
R. L. Stears
Keyword(s):  
Absorption Edge ◽  
Elemental Distribution ◽  
X Rays ◽  
Differential Absorption ◽  
Synchrotron Source ◽  
High Brightness ◽  
X Ray ◽  
Elemental Imaging ◽  
Cellular Integrity ◽  
X Ray Absorption

Because of the nature of the bacterial endospore, little work has been done on analyzing their elemental distribution and composition in the intact, living, hydrated state. The majority of the qualitative analysis entailed intensive disruption and processing of the endospores, which effects their cellular integrity and composition.Absorption edge imaging permits elemental analysis of hydrated, unstained specimens at high resolution. By taking advantage of differential absorption of x-ray photons in regions of varying elemental composition, and using a high brightness, tuneable synchrotron source to obtain monochromatic x-rays, contact x-ray micrographs can be made of unfixed, intact endospores that reveal sites of elemental localization. This study presents new data demonstrating the application of x-ray absorption edge imaging to produce elemental information about nitrogen (N) and calcium (Ca) localization using Bacillus thuringiensis as the test specimen.

Preparation of cultured astrocytes for x-ray microanalysis

1989 ◽  
Vol 47 ◽  
pp. 988-989
Author(s):  
N.K.R. Smith ◽  
K.E. Hunter ◽  
P. Mobley ◽  
L.P. Felpel
Keyword(s):  
Cultured Cells ◽  
Elemental Content ◽  
Elemental Distribution ◽  
Sprague Dawley ◽  
X Ray ◽  
Cultured Astrocytes ◽  
Freeze Dried ◽  
Ultimate Objective

Electron probe energy dispersive x-ray microanalysis (XRMA) offers a powerful tool for the determination of intracellular elemental content of biological tissue. However, preparation of the tissue specimen , particularly excitable central nervous system (CNS) tissue , for XRMA is rather difficult, as dissection of a sample from the intact organism frequently results in artefacts in elemental distribution. To circumvent the problems inherent in the in vivo preparation, we turned to an in vitro preparation of astrocytes grown in tissue culture. However, preparations of in vitro samples offer a new and unique set of problems. Generally, cultured cells, growing in monolayer, must be harvested by either mechanical or enzymatic procedures, resulting in variable degrees of damage to the cells and compromised intracel1ular elemental distribution. The ultimate objective is to process and analyze unperturbed cells. With the objective of sparing others from some of the same efforts, we are reporting the considerable difficulties we have encountered in attempting to prepare astrocytes for XRMA.Tissue cultures of astrocytes from newborn C57 mice or Sprague Dawley rats were prepared and cultured by standard techniques, usually in T25 flasks, except as noted differently on Cytodex beads or on gelatin. After different preparative procedures, all samples were frozen on brass pins in liquid propane, stored in liquid nitrogen, cryosectioned (0.1 μm), freeze dried, and microanalyzed as previously reported.

X-ray mapping without STEM

1994 ◽  
Vol 52 ◽  
pp. 508-509
Author(s):  
Judith M. Brock ◽  
Max T. Otten
Keyword(s):  
Life Science ◽  
Materials Science ◽  
Chemical Elements ◽  
Full Description ◽  
Scanning System ◽  
Elemental Distribution ◽  
X Ray ◽  
Transmission Electron ◽  
Distribution Of Elements ◽  
Made In

A knowledge of the distribution of chemical elements in a specimen is often highly useful. In materials science specimens features such as grain boundaries and precipitates generally force a certain order on mental distribution, so that a single profile away from the boundary or precipitate gives a full description of all relevant data. No such simplicity can be assumed in life science specimens, where elements can occur various combinations and in different concentrations in tissue. In the latter case a two-dimensional elemental-distribution image is required to describe the material adequately. X-ray mapping provides such of the distribution of elements.The big disadvantage of x-ray mapping hitherto has been one requirement: the transmission electron microscope must have the scanning function. In cases where the STEM functionality – to record scanning images using a variety of STEM detectors – is not used, but only x-ray mapping is intended, a significant investment must still be made in the scanning system: electronics that drive the beam, detectors for generating the scanning images, and monitors for displaying and recording the images.

3D Observation of Elemental Distribution of Si-Device using a Dedicated FIB/STEM System

2005 ◽  
Author(s):  
T. Yaguchi ◽  
M. Konno ◽  
T. Kamino ◽  
M. Ogasawara ◽  
K. Kaji ◽  
...  
Keyword(s):  
Focused Ion Beam ◽  
Ion Beam ◽  
Three Dimensional ◽  
Elemental Distribution ◽  
Multivariate Statistical ◽  
X Ray ◽  
Sample Rotation ◽  
Transmission Electron ◽  
Scanning Transmission ◽  
Elemental Maps

Abstract A technique for preparation of a pillar shaped sample and its multi-directional observation of the sample using a focused ion beam (FIB) / scanning transmission electron microscopy (STEM) system has been developed. The system employs an FIB/STEM compatible sample rotation holder with a specially designed rotation mechanism, which allows the sample to be rotated 360 degrees [1-3]. This technique was used for the three dimensional (3D) elemental mapping of a contact plug of a Si device in 90 nm technology. A specimen containing a contact plug was shaped to a pillar sample with a cross section of 200 nm x 200 nm and a 5 um length. Elemental analysis was performed with a 200 kV HD-2300 STEM equipped with the EDAX genesis Energy dispersive X-ray spectroscopy (EDX) system. Spectrum imaging combined with multivariate statistical analysis (MSA) [4, 5] was used to enhance the weak X-ray signals of the doped area, which contain a low concentration of As-K. The distributions of elements, especially the dopant As, were successfully enhanced by MSA. The elemental maps were .. reconstructed from the maps.

scholarly journals Deep learning-based denoising for improved dose efficiency in EDX tomography of nanoparticles

Nanoscale ◽  
2021 ◽  
Author(s):  
Alexander Skorikov ◽  
Wouter Heyvaert ◽  
Wiebke Albrecht ◽  
Daan Pelt ◽  
Sara Bals
Keyword(s):  
Deep Learning ◽  
Electron Tomography ◽  
Energy Dispersive ◽  
Elemental Distribution ◽  
X Ray ◽  
Powerful Approach ◽  
Dose Efficiency

The combination of energy-dispersive X-ray spectroscopy (EDX) and electron tomography is a powerful approach to retrieve the 3D elemental distribution in nanomaterials, providing an unprecedented level of information for complex,...

scholarly journals More than XRF Mapping: STEAM (Statistically Tailored Elemental Angle Mapper) a Pioneering Analysis Protocol for Pigment Studies

2021 ◽  
Vol 11 (4) ◽  
pp. 1446
Author(s):  
Jacopo Orsilli ◽  
Anna Galli ◽  
Letizia Bonizzoni ◽  
Michele Caccia
Keyword(s):  
Cultural Heritage ◽  
Element Distribution ◽  
Elemental Distribution ◽  
X Rays ◽  
Spectral Angle Mapper ◽  
X Ray ◽  
Fluorescence Radiation ◽  
Set Up ◽  
Non Destructive ◽  
Analysis Protocol

Among the possible variants of X-Ray Fluorescence (XRF), applications exploiting scanning Macro-XRF (MA-XRF) are lately widespread as they allow the visualization of the element distribution maintaining a non-destructive approach. The surface is scanned with a focused or collimated X-ray beam of millimeters or less: analyzing the emitted fluorescence radiation, also elements present below the surface contribute to the elemental distribution image obtained, due to the penetrative nature of X-rays. The importance of this method in the investigation of historical paintings is so obvious—as the elemental distribution obtained can reveal hidden sub-surface layers, including changes made by the artist, or restorations, without any damage to the object—that recently specific international conferences have been held. The present paper summarizes the advantages and limitations of using MA-XRF considering it as an imaging technique, in synergy with other hyperspectral methods, or combining it with spot investigations. The most recent applications in the cultural Heritage field are taken into account, demonstrating how obtained 2D-XRF maps can be of great help in the diagnostic applied on Cultural Heritage materials. Moreover, a pioneering analysis protocol based on the Spectral Angle Mapper (SAM) algorithm is presented, unifying the MA-XRF standard approach with punctual XRF, exploiting information from the mapped area as a database to extend the comprehension to data outside the scanned region, and working independently from the acquisition set-up. Experimental application on some reference pigment layers and a painting by Giotto are presented as validation of the proposed method.

scholarly journals Micro-Fabric Analyzer (MFA): A New Semiautomated ArcGIS-Based Edge Detector for Quantitative Microstructural Analysis of Rock Thin-Sections

2021 ◽  
Vol 10 (2) ◽  
pp. 51 ◽  
Author(s):  
Roberto Visalli ◽  
Gaetano Ortolano ◽  
Gaston Godard ◽  
Rosolino Cirrincione
Keyword(s):  
Physical Properties ◽  
Electron Backscatter Diffraction ◽  
Microstructural Analysis ◽  
Image Features ◽  
Elemental Distribution ◽  
Edge Detector ◽  
Sandstone Sample ◽  
Thin Sections ◽  
X Ray ◽  
Distribution Maps

Micro-Fabric Analyzer (MFA) is a new GIS-based tool for the quantitative extrapolation of rock microstructural features that takes advantage both of the characteristics of the X-ray images and the optical image features. Most of the previously developed edge mineral grain detectors are uniquely based on the physical properties of the X-ray-, electron-, or optical-derived images; not permitting the exploitation of the specific physical properties of each image type at the same time. More advanced techniques, such as 3D microtomography, permit the reconstruction of tridimensional models of mineral fabric arrays, even though adjacent mineral grain boundaries with the same atomic density are often not detectable. Only electron backscatter diffraction (EBSD) allows providing high-performing grain boundary detection that is crystallographically differentiated per mineral phase, even though it is relatively expensive and can be executed only in duly equipped microanalytical laboratories by suitably trained users. Instead, the MFA toolbox allows quantifying fabric parameters subdivided per mineral type starting from a crossed-polarizers high-resolution RGB image, which is useful for identifying the edges of the individual grains characterizing rock fabrics. Then, this image is integrated with a set of micro-X-ray maps, which are useful for the quantitative extrapolation of elemental distribution maps. In addition, all this is achieved by means of low-cost and easy-to-use equipment. We applied the tool on amphibolite, mylonitic-paragneiss, and -tonalite samples to extrapolate the particle fabric on different metamorphic rock types, as well as on the same sandstone sample used for another edge detector, which is useful for comparing the obtained results.

Comparison of Mo-10Nb Alloy Target Materials Prepared by Different Techniques

2017 ◽  
Vol 726 ◽  
pp. 316-320 ◽  
Author(s):  
Jie Gao ◽  
You Jun Lu ◽  
Jun Feng Hou ◽  
Zhen Xia Yuan ◽  
Wen Luo ◽  
...  
Keyword(s):  
Hot Pressing ◽  
Element Distribution ◽  
Raw Material ◽  
Elemental Distribution ◽  
X Ray Diffraction ◽  
X Ray ◽  
Alloy Target ◽  
Hot Pressing Sintering ◽  
Sintering Condition ◽  
Scanning Electron

The Mo powder and Nb powder was used as raw material, the Mo-10Nb alloy target was prepared by different sintering condition (non-pressure sintering and hot pressing sintering). The density, phase composition, microstructure and elemental distribution of Mo-10Nb alloy targets were determined by X-ray diffraction and scanning electron microscopy. The results showed that prepared by hot pressing Mo-10Nb alloy target density of 9.618 g/cm3, grain size 20 ~ 30μm, Mo and Nb element distribution.

Effects of Sintering Temperature on the Properties of Stainless Steel Foam

2015 ◽  
Vol 1087 ◽  
pp. 232-235
Author(s):  
Fazimah Mat Noor ◽  
N.I. Mad Rosip ◽  
Khairur Rijal Jamaludin ◽  
Sufizar Ahmad
Keyword(s):  
Stainless Steel ◽  
Average Pore Size ◽  
Vacuum Furnace ◽  
Stainless Steel 316L ◽  
Average Pore ◽  
X Ray ◽  
Replication Method ◽  
Pore Dimension ◽  
Steel Foam ◽  
Highly Porous

Foam replication method is capable of producing foams with a highly porous structure with adjustable pore dimension, shape and size. In this work, this method has been used to prepare stainless steel 316L foam and sintered at 1200°C, 1250°C and 1300°C in a vacuum furnace. The microstructure and elemental analysis of the sample were examined using scanning electron microscope (SEM) and Energy Dispersive X–Ray (EDX), while the mechanical properties of the samples was determined by using compression test. It was found that the average pore size was in the range of 330µm-350µm. The yield strength and elastic modulus are in the range of 58-66 GPa and 0.46-0.50GPa respectively.

Luminescence Properties of Eu2+ Doped Ca-α-SiAlON Phosphor

2010 ◽  
Vol 177 ◽  
pp. 277-280 ◽  
Author(s):  
Li Li ◽  
Cheng Zhang ◽  
Tao Feng ◽  
Hai Feng Xu ◽  
Qiang Li
Keyword(s):  
Fine Particles ◽  
Sintered Sample ◽  
Visible Spectral Region ◽  
Luminescence Properties ◽  
Elemental Distribution ◽  
High Adsorption ◽  
Soaking Time ◽  
X Ray ◽  
Large Numbers ◽  
Uv Visible

Eu2+ Doped Ca-α-SiAlON phosphor have been synthesized from SiO2, Al2O3, CaCO3, Eu(NO3)3,carbon powders by carbothermal reduction–nitridation (CRN). Using X-ray Diffractometer (XRD) and fluorescent spectrophotometer, the influences of the phase content of the sintered samples after different soaking time at 1390°C and their luminescence properties were studied. The pure Ca-α-SiAlON:Eu2+ were prepared at processing temperatures of 1390°C in a holding time of 8 h. Ca-α-SiAlON:Eu2+ had high adsorption in the UV–visible spectral region. Two bands were observed in the emission spectrum centered at about 459 and 545 nm exited at 290nm. And two excitation bands located at about 297nm, 300-400nm were observed in the excitation spectrum with monitored at emission wavelength of 469nm or 550nm respectively. The morphology of the samples was examined via SEM, TEM. Ca/Eu co-doped α-SiAlON powders had hollow sphere morphology and it is composed of large numbers of very fine particles of around 30 to 70 nm in diameter. Elemental distribution was investigated using an EDS attached to a scanning electron microscopy (SEM). The sintered sample has a composition commonly seen for α-SiAlON.

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