Monte Carlo Based Method for Conversion of In-Situ Gamma Ray Spectra Obtained with a Portable Ge Detector to an Incident Photon Flux Energy Distribution

1998 ◽  
Vol 74 (2) ◽  
pp. 216-230 ◽  
Author(s):  
A. Clouvas ◽  
S. Xanthos ◽  
M. Antonopoulos-Domis ◽  
J. Silva
2004 ◽  
Vol 72 (1-2) ◽  
pp. 163-168 ◽  
Author(s):  
A Likar ◽  
T Vidmar ◽  
M Lipoglavšek ◽  
G Omahen

Author(s):  
Ivana Grčić ◽  
Sanja Papić ◽  
Ivan Brnardić

Abstract The aim of this work was to evaluate the photocatalytic activity of two distinct anatase thin films. Films were prepared following the sol-gel procedure from titanium (IV) isopropoxide (TF-1) and from commercial TiO2 P25 as a starting material (TF-2). The films were compared based on the salicylic acid (2-dihydroxybenzoic acid, 2-HBA) photocatalytic degradation in reactors of different geometry and under different irradiation conditions. Experiments were performed in (i) an annular photoreactors operated under turbulent flow (TAR1 and TAR2) and (ii) semi-annular reactor operated under laminar flow (LFR). The TF-1 and TF-2 were immobilized on the inner side of outer wall of TAR1 and TAR2 and on the bottom of LFR. Experimental study included sorption study and four consecutive photocatalytic runs (tirr= 8 h) using TF-1 and TF-2 in each reactor. Obtained results confirmed the stability and the similar photocatalytic activity of the both films. The 2,5-dihydroxybenzoic acid (2,5-DHBA) and 2,3-dihydroxybenzoic acid (2,3-DHBA) were identified as main 2-HBA degradation by-products. Kinetic models were developed accordingly. Incident photon flux was determined along the inner reactor wall in annular reactors and on the bottom of LFR, i. e. on the thin film surface (Itf, W m−2) using ESSDE radiation emission model. The irradiation factor, i. e. the product of absorption coefficient and incident photon flux at film surface (μItf(z))m was introduced into the kinetic models. Resulting reaction rate constants ki (min−1W−0.5 m1.5) were independent of reactor geometry, hydrodynamics, irradiation condition and the optical properties of thin films. Efficiencies of TF-1 and TF-2 in studied reactors were given on the basis of quantum yields (QY) for 2-HBA oxidation and overall mineralization toward CO2.


2021 ◽  
Author(s):  
Emily Asenath-Smith ◽  
Emma Ambrogi ◽  
Lee Moores ◽  
Stephen Newman ◽  
Jonathon Brame

Subtle aspects of illumination sources and their characterization methods can introduce significant uncertainty into the data gathered from light-activated experiments, limiting their reproducibility and technology transition. Degradation kinetics of methyl orange (MO) and carbamazepine (CM) under illumination with TiO₂ were used as a case study for investigating the role of incident photon flux on photocatalytic degradation rates. Valerophenone and ferrioxalate actinometry were paired with optical radiometry in three different illumination systems: xenon arc (XE), tungsten halogen (W-H), and UV fluorescent (UV-F). Degradation rate constants for MO and CM varied similarly among the three light systems as k W-H < kiv-F < kXE, implying the same relative photon flux emission by each light. However, the apparent relative photon flux emitted by the different lights varied depending on the light characterization method. This discrepancy is shown to be caused by the spectral distribution present in light emission profiles, as well as absorption behavior of chemical actinometers and optical sensors. Data and calculations for the determination of photon flux from chemical and calibrated optical light characterization is presented, allowing us to interpret photo-degradation rate constants as a function of incident photon flux. This approach enabled the derivation of a calibrated ‘rate-flux’ metric for evaluating and translating data from photocatalysis studies.


Author(s):  
Tadao Tanaka ◽  
Taro Shimada ◽  
Takeshi Ito ◽  
Takenori Sukegawa

Nuclear facility sites such as an enrichment plant and fabrication plant are allowed to be released from the regulatory control of nuclear safety after the plants are decommissioned. It is necessary to confirm that the site has been decontaminated successfully, prior to be released. A determination method for U-238 concentration of background level in environment and for probate of vast site areas was proposed, in which the gamma-ray emission from the progeny radionuclides of U-238, such as Th-234, Pa-234m, Ra-226, are measured by in-situ gamma-ray spectrometry with a portable germanium semiconductor detector (portable Ge detector). Validity of the determination method of U-238 concentration from the progeny radionuclides was examined by the comparison between the U-238 concentration determined by the in-situ measurement with the portable Ge detector and that directly measured by ICP-MS. The U-238 concentration by the in-situ measurement was determined from peak counting rate at 186 keV of the gamma-ray emission corresponding to Ra-226. The determined U-238 concentration was in the order of 0.01 Bq/g in radioactive concentration, and was in comparable level with the concentrations decided by the ICP-MS. The proposed method utilizing gamma-ray estimation from the progeny radionuclides may be available for the U-238 concentration determination in vast land areas.


2009 ◽  
Vol 100 (11) ◽  
pp. 935-940 ◽  
Author(s):  
Jonas Boson ◽  
Agneta H. Plamboeck ◽  
Henrik Ramebäck ◽  
Göran Ågren ◽  
Lennart Johansson

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