A stainless steel with high capture cross section for thermal neutrons

1965 ◽  
Vol 18 (3) ◽  
pp. 302-304
Author(s):  
I. S. Lupakov ◽  
N. A. Vasil'ev
1941 ◽  
Vol 19a (3) ◽  
pp. 33-41 ◽  
Author(s):  
E. L. Harrington ◽  
J. L. Stewart

A comparison method of measuring, by using solutions, the capture cross-sections for thermal neutrons is described. The chief advantages are directness, simplicity, and freedom from uncertainties as to direction of path, or as to the magnitude of the scattering effect. The method is best suited to nuclei of large cross-sections. Assuming the well checked value for the cadmium nucleus to be correct, the capture cross-sections of certain other nuclei were determined. The results for barium and for hydrogen differ widely from values previously published.


1947 ◽  
Vol 25a (1) ◽  
pp. 26-41 ◽  
Author(s):  
H. G. Hereward ◽  
H. R. Paneth ◽  
G. C. Laurence ◽  
B. W. Sargent ◽  
A. M. Munn

The density distribution of thermal neutrons was measured with a small boron trifluoride chamber in a cylindrical tank containing 113 litres of heavy water in which lithium carbonate was dissolved. The diffusion length was found to be 22.7 cm. in this solution containing 7.70 × 10−4 atoms of lithium per molecule of heavy water (99.4 atom % D). After corrections were applied for the capture of neutrons in the heavy water and light hydrogen, the capture cross-section of lithium was found to be 59 × 10−24 cm.2 per atom for neutrons of standard velocity 2200 m. per sec. from the measured diffusion length and known transport mean free path.


2004 ◽  
Vol 41 (1) ◽  
pp. 1-6 ◽  
Author(s):  
Hideo HARADA ◽  
Shoji NAKAMURA ◽  
Toshiyuki FUJII ◽  
Hajimu YAMANA

2021 ◽  
Vol 12 ◽  
pp. 71
Author(s):  
N. Patronis ◽  
P. A. Assimakopoulos ◽  
S. Dababneh ◽  
M. Heil ◽  
F. Kaeppeler ◽  
...  

The neutron capture cross section of the unstable isotope $^{135}$Cs was measured relative to that of gold by means of the activation method. The sample was produced by ion implantation in a high resolution mass separator and irradiated with quasi-monoenergetic neutrons at 30 keV and 500 keV, using the $^{7}$Li(p,n)$^{7}$Be reaction. After the irradiations at the above energies, one more irradiation with thermal neutrons was used for defining the sample mass and for measuring the half-life of $^{136}$Cs. The neutron capture cross section was  determined as 164 $\pm$ 10 mbarn and 34.8 $\pm$ 3.0 mbarn at 30 keV and 500 keV, respectively, and were used to normalize the theoretically derived cross section shape.


1956 ◽  
Vol 69 (6) ◽  
pp. 469-479 ◽  
Author(s):  
R E Meads ◽  
C J England ◽  
C H Collie ◽  
G C Weeks

1975 ◽  
Vol 15 (02) ◽  
pp. 161-168
Author(s):  
Arthur H. Youmans ◽  
Eric C. Hopkinson

Abstract Commercially available logging services provide a measurement of the lifetime of thermal neutrons in formations adjacent to a borehole. This lifetime provides a measure of the macroscopic thermal neutron-capture cross-section S of the formation. which in turn is functionally related to the abundance and constituency of the rock matrix and contained fluids. Because the measurement is extremely sensitive to an abundance of trace elements like boron and gadolinium, it is very difficult to find rock formations with an accurately known value of S, which is required for the accuracy of the measuring system to be experimentally tested. Various theoretical studies published suggest that errors in the determination of S may occur because of the influence of borehole parameters and the effects of neutron diffusion. Experimental results are reported that demonstrate that the design of the instrument is crucial to the validity of any theoretical treatment of the subject. The influence of neutron diffusion and borehole effects can be overcome by optimal selection of spacing and shielding parameters. INTRODUCTION The lifetime of thermal neutrons in formation materials is a measure of the thermal neutron-capture cross-section of the bulk materials comprising the formation. This parameter, S, is quantitatively related to the elemental constituency of the medium. As such, a log based on the measurement of neutron lifetime1 can be used for identifying fluids in porous rocks when there is a contrast between the values of S for the respective fluids. Where formation waters are saline, the log has been used with great success to detect and evaluate oil-bearing zones behind casing. If S is accurately measured, it may be used to compute an unknown parameter with commensurate accuracy using the following relations.2Equation 1 whereEquation 2 The basic assumption of the logging method is that a population of neutrons in a formation will obey the simple relation N = Noe−Svt if the medium is homogeneous. In a medium penetrated by a borehole, it is assumed that the same kind of relation holds true after some time t1:Equation 3 From this equation, the value of S may be derived by measuring N1 and N2 at two times, t1 and t2.Equation 4 This theory requires two assumptions: that neutrons die or disappear only because of capture in the formation, and that it is possible to measure N, the number of live neutrons at any given time (or rather, the ratio of N1 to N2). About 10 years of commercial logging experience have established that S is, to all intents and purposes, accurately and reliably measured3 by the Neutron Lifetime Log (NLL). * This is true even though the foregoing assumptions are not rigorously true. Neutrons do diffuse4 during the measurement interval, with the result that some leave the formation and enter the borehole where their remaining lifetime is dependent on borehole parameters rather than on the formation. Also, the problem of sampling the neutron population is complicated by the fact that the spatial distribution of neutrons changes during the measurement interval, so that any sampling technique designed to measure N is prone to error, or at least subject to doubt.


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