Particle identification

Author(s):  
R.S. Gilmore
Author(s):  
J.M. Titchmarsh

The advances in recent years in the microanalytical capabilities of conventional TEM's fitted with probe forming lenses allow much more detailed investigations to be made of the microstructures of complex alloys, such as ferritic steels, than have been possible previously. In particular, the identification of individual precipitate particles with dimensions of a few tens of nanometers in alloys containing high densities of several chemically and crystallographically different precipitate types is feasible. The aim of the investigation described in this paper was to establish a method which allowed individual particle identification to be made in a few seconds so that large numbers of particles could be examined in a few hours.A Philips EM400 microscope, fitted with the scanning transmission (STEM) objective lens pole-pieces and an EDAX energy dispersive X-ray analyser, was used at 120 kV with a thermal W hairpin filament. The precipitates examined were extracted using a standard C replica technique from specimens of a 2¼Cr-lMo ferritic steel in a quenched and tempered condition.


2020 ◽  
Vol 1525 ◽  
pp. 012099
Author(s):  
Artem Ryzhikov ◽  
Denis Derkach ◽  
Mikhail Hushchyn ◽  

1997 ◽  
Vol 44 (4) ◽  
pp. 1621-1629 ◽  
Author(s):  
D. Boutigny ◽  
I. De Bonis ◽  
J. Favier ◽  
Y. Karyotakis ◽  
R. Lafaye ◽  
...  

2006 ◽  
Vol 15 (6) ◽  
pp. 1290-1302 ◽  
Author(s):  
Elena Iakhiaeva ◽  
Shakhawat Hossain Bhuiyan ◽  
Jiaming Yin ◽  
Christian Zwieb

2010 ◽  
Vol 15 (2) ◽  
pp. 218-223 ◽  
Author(s):  
Hendrik Hippchen ◽  
Wiebke H. Pohl ◽  
Peter J. Walla

Recently, it has been shown that 2-photon fluorescence correlation spectroscopy of single glycosylated 20-nm fluorescent spheres allows measurement of the relative carbohydrate binding affinities of unlabeled proteins and that these modified spheres can mimic the glycocalix of cell or virus surfaces. An especially useful extension would be the analysis of mixtures of nanospheres that each contain different fluorescent labels and are thus differentially “encoded.” If the surfaces of these encoded nanospheres are modified with various receptors, many different biomolecule-surface interactions and concurrent reactions can be measured quickly and simultaneously in a single-reaction vessel. An essential prerequisite for this general assay principle is the ability to identify with an accuracy of nearly 100% any encoded nanosphere present in a mixture on a single-particle level. Here the authors present a method that indeed allows certain identification of differently encoded nanospheres during single transits through the focal volume of a microscope objective (ø~200-500 nm) in aqueous solution. This opens the way for using the encoded nanospheres in 1-well measurements of a large variety of biomolecular receptor-ligand interactions, inhibition and concurrent reactions, and thus either for testing the behavior of ligands in a mimicked complex biomolecular environment or for a fast simultaneous measurement of a multitude of receptor-ligand interactions.


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