Progressing in the study of H2S oxidation at high pressure: Experiments and kinetic modelling

Author(s):  
Juan Colom ◽  
Ángela Millera ◽  
Rafael Bilbao ◽  
María Alzueta
2019 ◽  
Vol 56 (8) ◽  
pp. 3864-3876 ◽  
Author(s):  
Andréia Dalla Rosa ◽  
Alexander Junges ◽  
Ilizandra Aparecida Fernandes ◽  
Rogério Luis Cansian ◽  
Marcos L. Corazza ◽  
...  

2018 ◽  
Vol 133 ◽  
pp. 234-245 ◽  
Author(s):  
N.C. Leguizamon Guerra ◽  
J.C. Lizardo Huerta ◽  
C. Lorgeoux ◽  
R. Michels ◽  
R. Fournet ◽  
...  

ACS Omega ◽  
2020 ◽  
Vol 5 (12) ◽  
pp. 6937-6946
Author(s):  
Hirotaka Yokohama ◽  
Mélaz Tayakout-Fayolle ◽  
Aurélie Galfré ◽  
Naoki Fukumuro ◽  
Shinji Yae ◽  
...  

2017 ◽  
Vol 190 ◽  
pp. 824-834 ◽  
Author(s):  
Yang Li ◽  
Xinlei Yu ◽  
Hongjun Li ◽  
Qinghua Guo ◽  
Zhenghua Dai ◽  
...  

2013 ◽  
Vol 34 (1) ◽  
pp. 625-632 ◽  
Author(s):  
Chenlai (Ryan) Zhou ◽  
Karina Sendt ◽  
Brian S. Haynes

2011 ◽  
Vol 158 (8) ◽  
pp. 1444-1455 ◽  
Author(s):  
S. Vranckx ◽  
K.A. Heufer ◽  
C. Lee ◽  
H. Olivier ◽  
L. Schill ◽  
...  

Author(s):  
Marek Malecki ◽  
James Pawley ◽  
Hans Ris

The ultrastructure of cells suspended in physiological fluids or cell culture media can only be studied if the living processes are stopped while the cells remain in suspension. Attachment of living cells to carrier surfaces to facilitate further processing for electron microscopy produces a rapid reorganization of cell structure eradicating most traces of the structures present when the cells were in suspension. The structure of cells in suspension can be immobilized by either chemical fixation or, much faster, by rapid freezing (cryo-immobilization). The fixation speed is particularly important in studies of cell surface reorganization over time. High pressure freezing provides conditions where specimens up to 500μm thick can be frozen in milliseconds without ice crystal damage. This volume is sufficient for cells to remain in suspension until frozen. However, special procedures are needed to assure that the unattached cells are not lost during subsequent processing for LVSEM or HVEM using freeze-substitution or freeze drying. We recently developed such a procedure.


Sign in / Sign up

Export Citation Format

Share Document