scholarly journals The Importance of Complementary Information Provided by Surface Analysis, Electron Microscopy and in situ Characterization of Nanoparticles

2010 ◽  
Vol 16 (S2) ◽  
pp. 408-409 ◽  
Author(s):  
DR Baer ◽  
JE Amonette ◽  
A Dohnalkova ◽  
MH Engelhard ◽  
S Kuchibhatla ◽  
...  

Extended abstract of a paper presented at Microscopy and Microanalysis 2010 in Portland, Oregon, USA, August 1 – August 5, 2010.

2004 ◽  
Vol 10 (S02) ◽  
pp. 1056-1057
Author(s):  
Eric Doehne ◽  
Tiziana Lombardo

Extended abstract of a paper presented at Microscopy and Microanalysis 2004 in Savannah, Georgia, USA, August 1–5, 2004.


2001 ◽  
Vol 7 (S2) ◽  
pp. 1058-1059
Author(s):  
P.A. Crozier

Controlled atmosphere electron microscopy (CAEM) is a form of in situ microscopy in which the sample is exposed to a reactive gas during observation. This instrument essentially combines the nano-structural characterization features of a TEM with a microreactor and is ideal for studying gas/solid reactions in catalysts. Such in situ techniques can provide a link between surface studies performed under UHV conditions and catalytic reactions run in high-pressure reactors. with correctly designed experiments, CAEM is a powerful technique for correlating dynamic changes in microstructure with catalysis and can be used to provide insights on the location of active sites and mechanisms for catalysis. Baker and colleagues have worked for over thirty years on different heterogeneous catalysts using in situ electron microscopy (see [1] for example). Gai has also published many studies on the application of CAEM to oxide catalysts [2].The technique usually relies on detecting a change in the heterogeneous catalyst during a catalytic reaction.


Reproduction ◽  
2000 ◽  
pp. 325-335 ◽  
Author(s):  
A Calvo ◽  
LM Pastor ◽  
S Bonet ◽  
E Pinart ◽  
M Ventura

Lectin histochemistry was used to perform in situ characterization of the glycoconjugates present in boar testis and epididymis. Thirteen horseradish peroxidase- or digoxigenin-labelled lectins were used in samples obtained from healthy fertile boars. The acrosomes of the spermatids were stained intensely by lectins with affinity for galactose and N-acetyl-galactosamine residues, these being soybean, peanut and Ricinus communis agglutinins. Sertoli cells were stained selectively by Maackia ammurensis agglutinin. The lamina propria of seminiferous tubules showed the most intense staining with fucose-binding lectins. The Golgi area and the apical part of the principal cells of the epididymis were stained intensely with many lectins and their distribution was similar in the three zones of the epididymis. On the basis of lectin affinity, both testis and epididymis appear to have N- and O-linked glycoconjugates. Spermatozoa from different epididymal regions showed different expression of terminal galactose and N-acetyl-galactosamine. Sialic acid (specifically alpha2,3 neuraminic-5 acid) was probably incorporated into spermatozoa along the extratesticular ducts. These findings indicate that the development and maturation of boar spermatozoa are accompanied by changes in glycoconjugates. As some lectins stain cellular or extracellular compartments specifically, these lectins could be useful markers in histopathological evaluation of diseases of boar testis and epididymis.


1983 ◽  
Author(s):  
K. Arulanandan ◽  
Y. Dafalias ◽  
L. R. Herrmann ◽  
A. Anandarajah ◽  
N. Meegoda

2016 ◽  
Vol 108 (21) ◽  
pp. 211902 ◽  
Author(s):  
Xian Chen ◽  
Nobumichi Tamura ◽  
Alastair MacDowell ◽  
Richard D. James

ACS Catalysis ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 1464-1484 ◽  
Author(s):  
Yong Han ◽  
Hui Zhang ◽  
Yi Yu ◽  
Zhi Liu

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