Thermal dissociation of streptavidin homotetramer in the gas phase: Subunit loss versus backbone fragmentation

2013 ◽  
Vol 345-347 ◽  
pp. 97-103 ◽  
Author(s):  
Elena N. Kitova ◽  
Igor Sinelnikov ◽  
Lu Deng ◽  
John S. Klassen
Keyword(s):  
Gas Phase ◽  
Thermal Dissociation

Thermal dissociation of protonated cyclodextrin-amino acid complexes in the gas phase

2001 ◽  
Vol 210-211 ◽  
pp. 215-222 ◽  
Author(s):  
Ben Garcia ◽  
Javier Ramirez ◽  
Sandy Wong ◽  
Carlito B. Lebrilla
Keyword(s):  
Amino Acid ◽  
Gas Phase ◽  
Thermal Dissociation ◽  
Amino Acid Complexes

Mechanism of HOxFormation in the Gas-Phase Ozone-Alkene Reaction. 2. Prompt versus Thermal Dissociation of Carbonyl Oxides to Form OH

2001 ◽  
Vol 105 (18) ◽  
pp. 4446-4457 ◽  
Author(s):  
Jesse H. Kroll ◽  
Shailesh R. Sahay ◽  
James G. Anderson ◽  
Kenneth L. Demerjian ◽  
Neil M. Donahue
Keyword(s):  
Gas Phase ◽  
Thermal Dissociation ◽  
Carbonyl Oxides

Thermal dissociation of ions limits the degree of the gas-phase H/D exchange at the atmospheric pressure

2017 ◽  
Vol 52 (4) ◽  
pp. 204-209 ◽  
Author(s):  
Y. Kostyukevich ◽  
A. Kononikhin ◽  
I. Popov ◽  
E. Nikolaev
Keyword(s):  
Gas Phase ◽  
Atmospheric Pressure ◽  
Thermal Dissociation

scholarly journals Thermal dissociation of the protein homodimer ecotin in the gas phase

2002 ◽  
Vol 13 (12) ◽  
pp. 1432-1442 ◽  
Author(s):  
Natalia Felitsyn ◽  
Elena N. Kitova ◽  
John S. Klassen
Keyword(s):  
Gas Phase ◽  
Thermal Dissociation

Synthesis of α- and β-Rhombohedral Boron Powders via Gas Phase Thermal Dissociation of Boron Trichloride by Hydrogen

2011 ◽  
Vol 42 (3) ◽  
pp. 568-574 ◽  
Author(s):  
Duygu Ağaoğulları ◽  
Özge Balcı ◽  
İsmaİl Duman ◽  
M. Lütfİ Öveçoğlu
Keyword(s):  
Gas Phase ◽  
Thermal Dissociation ◽  
Boron Trichloride ◽  
Rhombohedral Boron

scholarly journals Peculiarities of thermal dissociation of oxides during submerged arc welding

2013 ◽  
Vol 18 (4) ◽  
pp. 314-321 ◽  
Author(s):  
Leonid Zhdanov ◽  
Vladyslav Kovalenko ◽  
Nataliya Strelenko ◽  
Yevgenia Chvertko
Keyword(s):  
Gas Phase ◽  
Arc Welding ◽  
Linear Equations ◽  
Thermal Dissociation ◽  
Submerged Arc Welding ◽  
Welding Fluxes ◽  
Vapour Mixture ◽  
Definition Of ◽  
Submerged Arc ◽  
Non Linear Equations

A method of settlement of the process of thermal dissociation of oxides in reaction zone during the submerged arc welding and welding deposition is presented. Combined non-linear equations for definition of gas-vapour mixture composition were developed. They describe the dissociation of MeO, MeO2 and Me2O3 types of oxides. Calculations of the processes of oxide dissociation were performed for the oxides that are commonly included into welding fluxes. Their results and analysis are presented. The method proposed appeared to be adequate and applicable for analysis of processes during submerged arc operation that run in the gas phase.

Residual Gas Reactions in the Electron Microscope: I. Qualitative Observations on the Water Gas Reaction

1968 ◽  
Vol 26 ◽  
pp. 292-293
Author(s):  
Richard E. Hartman ◽  
Roberta S. Hartman ◽  
Peter L. Ramos
Keyword(s):  
Electron Beam ◽  
Electron Microscope ◽  
Gas Phase ◽  
Absolute Temperature ◽  
Residual Gas ◽  
Gas Reactions ◽  
Image Position ◽  
The Right ◽  
Water Gas ◽  
Thinning Rate

The action of water and the electron beam on organic specimens in the electron microscope results in the removal of oxidizable material (primarily hydrogen and carbon) by reactions similar to the water gas reaction .which has the form:The energy required to force the reaction to the right is supplied by the interaction of the electron beam with the specimen.The mass of water striking the specimen is given by:where u = gH2O/cm2 sec, PH2O = partial pressure of water in Torr, & T = absolute temperature of the gas phase. If it is assumed that mass is removed from the specimen by a reaction approximated by (1) and that the specimen is uniformly thinned by the reaction, then the thinning rate in A/ min iswhere x = thickness of the specimen in A, t = time in minutes, & E = efficiency (the fraction of the water striking the specimen which reacts with it).

Integration of Core-Edge Spectroscopy Methods for the Study of Polymers

1996 ◽  
Vol 54 ◽  
pp. 154-155
Author(s):  
E. G. Rightor
Keyword(s):  
Excited State ◽  
Polymer Blends ◽  
Gas Phase ◽  
Spatial Resolution ◽  
High Spatial Resolution ◽  
Electronic States ◽  
Core Electron ◽  
Bulk Solids ◽  
Development Application

Core edge spectroscopy methods are versatile tools for investigating a wide variety of materials. They can be used to probe the electronic states of materials in bulk solids, on surfaces, or in the gas phase. This family of methods involves promoting an inner shell (core) electron to an excited state and recording either the primary excitation or secondary decay of the excited state. The techniques are complimentary and have different strengths and limitations for studying challenging aspects of materials. The need to identify components in polymers or polymer blends at high spatial resolution has driven development, application, and integration of results from several of these methods.

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