Reactions of Large Water Cluster Anions with Hydrogen Chloride:  Formation of Atomic Hydrogen and Phase Separation in the Gas Phase

2007 ◽  
Vol 129 (11) ◽  
pp. 3238-3246 ◽  
Author(s):  
Chi-Kit Siu ◽  
O. Petru Balaj ◽  
Vladimir E. Bondybey ◽  
Martin K. Beyer
2009 ◽  
Vol 130 (12) ◽  
pp. 124319 ◽  
Author(s):  
Ádám Madarász ◽  
Peter J. Rossky ◽  
László Turi

1993 ◽  
Vol 48 (5) ◽  
pp. 3764-3770 ◽  
Author(s):  
Byung Jin Mhin ◽  
Sang Joo Lee ◽  
Kwang S. Kim

1997 ◽  
Vol 101 (18) ◽  
pp. 3540-3546 ◽  
Author(s):  
Kyung-Ah Son ◽  
John L. Gland
Keyword(s):  

1987 ◽  
Vol 5 (1) ◽  
Author(s):  
Roger Atkinson ◽  
SaraM. Aschmann ◽  
ErnestoC. Tuazon ◽  
MarkA. Goodman ◽  
ArthurM. Winer

2013 ◽  
Vol 78 (12) ◽  
pp. 2115-2130 ◽  
Author(s):  
Martinez Gonzalez ◽  
Tanja Vidakovic-Koch ◽  
Rafael Kuwertz ◽  
Ulrich Kunz ◽  
Thomas Turek ◽  
...  

Hydrogen chloride (HCl) oxidation has been investigated on technical membrane electrode assemblies in a cyclone flow cell. Influence of Nafion loading, temperature and hydrogen chloride mole fraction in the gas phase has been studied. The apparent kinetic parameters like reaction order with respect to HCl, Tafel slope and activation energy have been determined from polarization data. The apparent kinetic parameters suggest that the recombination of adsorbed Cl intermediate is the rate determining step.


2001 ◽  
Vol 79 (1) ◽  
pp. 36-38 ◽  
Author(s):  
Jae Yeol Maeng ◽  
Sehun Kim ◽  
S. K. Jo ◽  
W. P. Fitts ◽  
J. M. White

2010 ◽  
Vol 29 (13) ◽  
pp. 3001-3006 ◽  
Author(s):  
Robert F. Höckendorf ◽  
Yali Cao ◽  
Martin K. Beyer

2021 ◽  
Author(s):  
Katerina Djambazova ◽  
Martin Dufresne ◽  
Lukasz Migas ◽  
Angela Kruse ◽  
Raf Van de Plas ◽  
...  

Gangliosides are classified as acidic glycosphingolipids, containing ceramide moieties and oligosaccharide chains with one or multiple sialic acid residue(s). The presence of multiple sialylation sites gives rise to highly diverse isomeric structures with distinct biological roles. Matrix-assisted laser desorption/ionization imaging mass spectrometry (MALDI IMS) enables the untargeted spatial analysis of gangliosides, among other biomolecules, directly from tissue sections. Integrating trapped ion mobility mass spectrometry (TIMS), a gas-phase separation technology, with MALDI IMS allows for the investi-gation of isomeric lipid structures in situ. Here we demonstrate the gas-phase separation of disialoganglioside isomers GD1a and GD1b that differ in the position of a sialic acid residue, in a standard mixture of both isomers, a total ganglioside extract, and directly from thin tissue sections. The unique spatial distributions of GD1a/b (d36:1) and GD1a/b (d38:1) were deter-mined from rat hippocampus, as well as in a spinal cord tissue section.


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