Direct determination of the limiting high-pressure rate constants of the system fluorosulfate radical + fluorosulfate radical .dblharw. peroxydisulfuryl difluoride over the temperature range 293-381 K

1989 ◽  
Vol 93 (8) ◽  
pp. 3089-3094 ◽  
Author(s):  
C. J. Cobos ◽  
A. E. Croce de Cobos ◽  
H. Hippler ◽  
E. Castellano
2000 ◽  
Vol 329 (3-4) ◽  
pp. 191-199 ◽  
Author(s):  
E. Martı́nez ◽  
J. Albaladejo ◽  
E. Jiménez ◽  
A. Notario ◽  
Y. Dı́az de Mera

1986 ◽  
Vol 39 (8) ◽  
pp. 1257 ◽  
Author(s):  
NL Arthur ◽  
JC Biordi

Rate constants for the recombination of CH3 radicals have been measured by means of the rotating sector technique in the temperature range 373- 463 K, and at a pressure of 30 Torr . CH3 radicals were produced by the photolysis of acetone, and the experimental data were fitted to sector curves generated from Shepp's theory. The results give kb = (2.81�0.22)×1013 cm3 mol-1 s-1, which, under the chosen experimental conditions, is close to its high-pressure limiting value. A comparison is made with the other values of the rate constant reported in the literature, and a best value is suggested.


1975 ◽  
Vol 30 (8) ◽  
pp. 951-954 ◽  
Author(s):  
K. Frohnecke ◽  
H. Fischbach

Abstract Direct Determination of the Rate Constants for the Sr-and Ba-exchange Between the Small and Large Channels in LMS 13X The rate constants for the intracristalline Sr-and Ba-exchange between the small and large diameter channels of LMS 13X were measured. For this matter the method of interrupting the ion exchange was modified. It is assumed, that a first order reaction takes place. Using the rate constants and the diffusion coefficients, which were measured by Hoinkis and Levi, the total exchange of Sr 2+ and Ba 2+ could be calculated.


1980 ◽  
Vol 58 (6) ◽  
pp. 900-904
Author(s):  
N. Kaplan ◽  
S. N. Sharma ◽  
D. Ll. Williams

A nuclear magnetic resonance study of 115In in a single crystal of InBi has enabled the direct determination of the isotropic and anisotropic Knight shifts as well as the quadrupole interaction over the temperature range between 1.2 K and room temperature. An essentially linear variation with temperature is obtained for all three parameters with both the quadrupole interaction and the isotropic Knight shifts undergoing sign reversals in this temperature range. Comparisons are made with earlier nmr and time differential perturbed angular correlation (TDPAC) studies as well as with band structure predictions.


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