scholarly journals Creating a Detector Response Matrix for the Micro-Calorimeter

2020 ◽  
Author(s):  
Ernst Esch
2014 ◽  
Author(s):  
J. Barylak ◽  
P. Podgórski ◽  
T. Mrozek ◽  
A. Barylak ◽  
M. Stęślicki ◽  
...  

ANRI ◽  
2021 ◽  
Vol 0 (2) ◽  
pp. 54-64
Author(s):  
Aliaksei Zaharadniuk ◽  
Dmitri Abalonski ◽  
Raman Lukashevich

The paper considers an algorithm for correcting the instrumental spectrum of the gamma-radiometer with a NaI(Tl) detector. The algorithm is based on the ME-LM method (Maximum Likelihood Estimation using Expectation Maximization), which uses a detector response matrix obtained by Monte Carlo simulation. The main advantage of the algorithm is the rescaling procedure, which significantly reduces the spectrum processing time.


ANRI ◽  
2020 ◽  
Vol 0 (4) ◽  
pp. 14-28
Author(s):  
Aliaksei Zaharadniuk ◽  
Roman Lukashevich ◽  
Konstantin Syankovsky ◽  
Aleksandr Novichenko

The paper considers an improved method for correcting the instrumental spectrum of a high purity germanium detector (HPGe detector) in the energy range (10–300 keV). The method uses a detector response matrix obtained by the Monte Carlo method, which allows to bring the appearance of the instrumental spectrum of the HPGe detector closer to its true shape by minimizing the influence of the detector response function. The main difference of this method from analogs is the additional deconvolution algorithm of the corrected spectrum, which makes it possible to obtain a smooth curve at the output.


Author(s):  
RunLong Gao ◽  
Yang Liu ◽  
XiaoPing Ouyang ◽  
Jing Chen ◽  
Xiao Ouyang

1998 ◽  
Vol 08 (PR3) ◽  
pp. Pr3-233-Pr3-236
Author(s):  
M. Frericks ◽  
H. F.C. Hoevers ◽  
P. de Groene ◽  
W. A. Mels ◽  
P. A.J. de Korte

1983 ◽  
Vol 48 (3) ◽  
pp. 722-734
Author(s):  
Martin Koval

The flame ionisation detector response to C6-C11 aliphatic hydrocarbon solutions in carbon disulphide in the concentration range between 1.3-9.5 mg ml-1 retained lineary despite the excess of solvent entering the detector simultaneously with the analyte. Pure carbon disulphide exhibited a small positive detector response which did not interfere in calibration procedure and which, under certain GC conditions, inverted to negative values. This response was not proportional to the injected volume and was strongly influenced by the column temperature and/or bleed. On the basis of these findings, a method compatible with the widely used charcoal tube carbon disulphide desorption procedure was developed and evaluated. It consists of static desorption of the sum of aliphatic alkanes and cycloalkanes from the activated charcoal after which an internal standard is added to the supernatant eluate. The resulting carbon disulphide solution is analysed on a highly polar stationary phase 1,2,3-tris(2-cyanoethoxy)propane where the solvent and the analyte coelute in a single peak, the height of which is practically proportional to the sum of alkanes and cycloalkanes present. This also makes determinations of other substances present in the sample more simple. The field test of the proposed method yielded values comparable in precision and accuracy with a control infrared spectrophotometric method.


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