Kinetic Rate Law Issues in the Morphological Relaxation of Rippled Crystal Surfaces

Author(s):  
Jonah D. Erlebacher
2013 ◽  
Vol 351 ◽  
pp. 299-309 ◽  
Author(s):  
Ravi K.P. Gudavalli ◽  
Yelena P. Katsenovich ◽  
Dawn M. Wellman ◽  
Melina Idarraga ◽  
Leonel E. Lagos ◽  
...  

2003 ◽  
Author(s):  
David London ◽  
G B Morgan ◽  
J P Icenhower ◽  
B P McGrail ◽  
A Luttge

1987 ◽  
Vol 64 (11) ◽  
pp. 925 ◽  
Author(s):  
Fernando Mata-Perez ◽  
Joaquin F. Perez-Benito

2003 ◽  
Vol 807 ◽  
Author(s):  
P. Frugier ◽  
S. Gin ◽  
C. Jégou

ABSTRACTSimplified glass compositions were chosen to improve our knowledge of the alteration kinetics of complex glasses dedicated to the confinement of high-level waste. Since 1998, the sodium borosilicate glass system is at the center of a passionate debate between an affinity-based kinetic rate law and a protective surface layer theory. All the authors who have investigated ternary 68/14/18 SiO2–B2O3–Na2O glass agree on the fact that the affinity law cannot satisfactorily account for its alteration kinetics. Some authors explained that these discrepancies between classical kinetic rate law and experimental findings could be due to macromolecular amorphous separation in the 68/14/18 sodium borosilicate system and that this simplified glass could be divided into 90% reedmergnerite (NaBSi3O8) and 10% diborate (Na2O–2B2O3). This article provides evidence of the homogeneity of ternary 68/18/14 SiO2–B2O3–Na2O glass at nanometric scale and shows that even phase separation at less than nanometric scale could not explain the inability of hydrated glass-solution affinity laws to describe its alteration. The relative simplicity of the SiO2–B2O3–Na2O chemical system allows a critical examination of the macroscopic alteration laws developed over the last twenty years based only on the hydrated glass-solution chemical affinity without taking into account the formation and reactivity of the gel or its passivating properties.


1984 ◽  
Vol 62 (9) ◽  
pp. 1835-1839 ◽  
Author(s):  
Donald G. Lee ◽  
Ligaya N. Congson ◽  
Udo A. Spitzer ◽  
Merle E. Olson

The oxidation of 2-propanol and cyclobutanol by stoichiometric amounts of sodium ruthenate has been studied. Contrary to previously published speculations, it has been found that these reactions are not initiated by traces of perruthenate present as a contaminant in the ruthenate solutions. This conclusion is supported by both the kinetic rate law for the reaction and the products obtained from the oxidation of alcohols that would be expected to react differently with [Formula: see text] and [Formula: see text].


2015 ◽  
Vol 47 (6) ◽  
pp. 351-360 ◽  
Author(s):  
Andriy Kytsya ◽  
Liliya Bazylyak ◽  
Yuriy Hrynda ◽  
Andriy Horechyy ◽  
Yuriy Medvedevdkikh

2002 ◽  
Vol 713 ◽  
Author(s):  
B. P. McGrail ◽  
J. P. Icenhower ◽  
E. A. Rodriguez

ABSTRACTDiscrepancies between classical kinetic rate law theory and experiment were quantitatively assessed and found to correlate with macromolecular amorphous separation in the sodium borosilicate glass system. A quantitative reinterpretation of static corrosion data and new SPFT data shows that a recently advanced protective surface layer theory fails to describe the observed dissolution behavior of simple and complex silicate glasses under carefully controlled experimental conditions. The hypothesis is shown to be self-inconsistent in contrast with a phase separation model that is in quantitative agreement with experiments.


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