• Journal of Nuclear Fuel Cycle and Waste Technology(JNFCWT)
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• v.12 no.2
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• pp.153-164
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• 2014

Currently, there are many programs which are now being developed or already developed to predict radionuclide and corrosion product at the stage of designing NPP. However, since there are not many developments in evaluating quantity of activation corrosion products occurring when disassembling a nuclear power plant there exist some difficulties in calculating accurately. In order to evaluate activation products inventory for the research of effect of neutron activation in the reactor vessel, component of nuclear reactor and adjacent structures, it should be evaluated by using operation history of nuclear reactor, material composition of structure and average neutron flux in every field representing fixed structure of nuclear reactor. In this study, CORA, PACTOLE, CRUDSIM, CREAT and ACE codes are analyzed to predict the quantity of radionuclide and corrosion product of primary reactor which is used at the stage of designing. As a future study, the accuracy in calculating the quantity of product corrosion can be increase by finding out the possibility of use and improvement for evaluation of the decontamination.

• Korean Journal of Food Science and Technology
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• v.3 no.3
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• pp.144-149
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• 1971

The sensitive technique of activation analysis is well suited for this study since the elements such as As, Br, and Se in tobaccoes are expected to be high concentration. As, Br, and Hg were determined by Bethge destruction method and subsequent neutron activation analysis. $^{77m}Se$ was also by non-destruction activation analysis. The quantities of the element determined in Korean tobaccoes are given as follows in ppm: As, 0.65 ppm. Hg, 0.74 ppm. Se, 1.18 ppm. Br, 7.1 ppm. From the date given it seems that Korean tobaccoes and foreign tobaccoes contained considerably high concentration of selenium and mercury.

• Nuclear Engineering and Technology
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• v.34 no.6
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• pp.566-573
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• 2002

Neutron activation analysis based on $textsc{k}$$_{o}$-standardization method＃ ($textsc{k}$o-NAA) is Com as one of the most remarkable progresses of the NAA with advantages of experimental simplicity, high accuracy, excellent flexibility with respect to irradiation and counting conditions, and suitability for computerization. This study was carried out to determine the reactor neutron spectrum parameters, i.e. $\alpha$ and f as the main factors of irradiation quality at NAA ＃1 irradiation hole on HANARO research reactor, to evaluate peak detection efficiency of the gamma-ray spectrometer for the use in the $textsc{k}$$_{o}$ experiments and to compare the measured concentration results with the certified values of some SRMs applying the experimentally determined to-parameters.ers.

• Proceedings of the Korean Nuclear Society Conference
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• 1996.05a
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• pp.197-201
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• 1996

In the detail reaction-rate measurements in a critical assembly using the foil activation method, the measured activations of detector foils have inevitably errors caused by detector foil self-shielding effect. If neutron flux could be approximated to Westcott flux: i.e. well thermalized Maxwellian distribution, these activations of detector foil could be corrected to represent the unperturbated flux at any detected position in the cell with using Westcott option and reaction-rate option of the lattice code, WIMS-AECL. These calculated detector material self-shielding correction factors of the tested fuel, CANFLEX provided much information about neutron spectrum of test lattice cell as well as the correction factors themselves. The results could be verified by another lattice calculations.

• Analytical Science and Technology
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• v.16 no.5
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• pp.358-367
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• 2003

In this research, first of all, the analytical methods for the determination of major elements in sediment have been developed with ICP-MS (Inductively Coupled Plasma Mass Spectrometry). The analytical results of major elements (Al, Ca, K, Fe, Mg) with Cool ICP-MS were much better than those with normal ICP-MS. The analytical results were compared with those of NAA (Neutron Activation Analysis). NAA were a little superior to ICP-MS for the determination of major elements in sediment as a non-destructive trace analytical method. The analytical methods for the determination of minor elements (Cr, Ce, U, Co, Pb, As, Se) have been also developed with ICP-MS. The analytical results by standard calibration curve with ICP-MS were not accurate due to the matrix interferences. Thus, the internal standard method was applied, then the analytical results for minor elements with ICP-MS were greatly improved. The analytical results obtained by ICP-MS were compared with those obtained by NAA. It showed that the two analytical methods have great capabilities for the determination of minor elements in sediments. Accordingly, the NAA will play an important role in analysis of environment sample with complex matrix. ICP-MS also will play an important role because it has a great capability for the determination of Pb that could not be determined by NAA.

• Proceedings of the Korean Society of Medical Physics Conference
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• 2002.09a
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• pp.161-163
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• 2002

The BNCT(Boron Neutron Capture Therapy) facility has been developed in Hanaro(High-flux Advanced Neutron Application Reactor), a research reactor of Korea Atomic Energy Research Institute. A typical tangenial beam port is utilized with this BNCT facility. Thermal neutrons can be penetrated within the limits of the possible maximum instead of being filtered fast neutrons and gamma rays as much as possible using the silicon and bismuth single crystals. In addition to, the liquid nitrogen (LN$_2$) is used to cool down the silicon and bismuth single crystals for the increase of the penetrated thermal neutron flux. Neutron beams for BNCT are shielded using the water shutter. The water shutter was designed and manufactured not to interfere with any other subsystem of Hanaro when the BNCT facility is operated. Also, it is replaced with conventional beam port plug in order to cut off helium gas leakage in the beam port. A circular collimator, composed of $\^$6/Li$_2$CO$_3$ and polyethylene compounds, is installed at the irradiation position. The measured neutron flux with 24 MW reactor power using the Au-198 activation analysis method is 8.3${\times}$10$\^$8/ n/cm$^2$ s at the collimator, exit point of neutron beams. Flatness of neutron beams is proven to ${\pm}$ 6.8% at 97 mm collimator. According to the result of acceptance tests of the water shutter, the filling time of water is about 190 seconds and drainage time of it is about 270 seconds. The radiation leakages in the irradiation room are analyzed to near the background level for neutron and 12 mSv/hr in the maximum for gamma by using BF$_3$ proportional counter and GM counter respectively. Therefore, it is verified that the neutron beams from BNCT facility in Hanaro will be enough to utilize for the purpose of clinical and pre-clinical experiment.

• Bulletin of the Korean Chemical Society
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• v.7 no.6
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• pp.438-442
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• 1986

A number of Korean potsherd samples has been classified by Fisher's discriminant method for the training set of Kyungki, Koryung and Kyungnam groups. The Koryung samples have been further classified for the training set of Koryung A, B and C subgroups. The training sets have been used to define classification of unknown samples and clay samples so as to find out some similarity between clay samples and certain potsherd groups.

• Analytical Science and Technology
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• v.15 no.4
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• pp.365-372
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• 2002

In this study, inorganic elemental distribution in Korean adult human tissue of liver, lung, muscle, kidney, rib and thyroid has been investigated. These tissues were collected from human's body within 48 hours after their death according to IAEA's recommended method, dried by freeze drying method and then pulverized. Neutron activation analysis was applied to these samples to determine the concentrations of 5 major elements of Ca, Mg, Na, K, and Cl and 12 trace elements of Mn, I, Sr, As, Br, Co, Cr, Cs, Fe, Rb, Se, and Zn. To confirm accuracy of analytical result was performed using three kinds of standard reference materials and resulted that the relative error is within 10% for the most of elements and the Z-score indicating a performance of analysis is within 2. The elemental distribution shows that the major elements are distributed homogeneously with a specific concentration and that the trace elements shows a distribution of different concentration with kinds of tissue and their age. Particularly, iodine shows higher concentration with 1000 ${\mu}g/g$ in thyroid, and calcium and strontium show the concentration with 15.9% and 84.4 ${\mu}g/g$ in rib, respectively.

• Journal of the Korean Society of Groundwater Environment
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• v.5 no.4
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• pp.210-214
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• 1998

In general the concentration of uranium in natural water such as fresh water and sea water is in the range of 0.01∼5 ppb, therefore trace analytical technique is required. The aim of present work is to compare a direct and preconcentration methods by evaporation and to investigate rapid and accurate trace analysis of uranium in groundwater using Instrumental Neutron Activation Analysis (INAA) which are sensitive and nondestructive method. Identification of analytical procedure was carried out using uranium standard solution of the range of 0.5∼100 ppb. In the given concentration, the deviation of calibration curve was less than 2%, and the standard deviation of measured values at each concentration was the range of 2∼12%. The difference of U content with sampling time for the same sample site was about 10.3%. Using this established method, the concentrations of uranium in samples collected at the 17 spring of Choongchung areas were found to be in the range of 1∼80 ppb.

• Nuclear Engineering and Technology
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• v.5 no.4
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• pp.279-285
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• 1973

A method for the simultaneous determination of mercury, bromine, arsenic and cadmium in biological samples is described. Following neutron activation and a simple distillation of volatile compounds, mercury and bromine were determined by gamma-ray spectrometry. Arsenic and cadmium were further separated by cation exchange separation and determined similarly. Determination limits for mercury, bromine, arsenic and cadmium were 0.001$\mu\textrm{g}$, 0.003$\mu\textrm{g}$, 0.001$\mu\textrm{g}$ and 0.02$\mu\textrm{g}$, respectively. The method has been applied to the determination of mercury, bromine, arsenic and cadmium in rice and fish samples. Analysis of a standard kale powder yielded the values of 0.046$\mu\textrm{g}$/g for mercury, 24.5$\mu\textrm{g}$/g for bromine 0.17 $\mu\textrm{g}$/g for arsenic and 0.50$\mu\textrm{g}$/g for cadmium.