• Nuclear Engineering and Technology
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• v.55 no.6
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• pp.2158-2165
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• 2023

Marine radioactivity monitoring is critical for taking immediate action in case of unexpected nuclear accidents at nuclear facilities located near coastal areas. Especially when the level of contamination is not predictable, mobile monitoring systems will be useful for wide-area ocean radiation survey and for determination of the level of radioactivity. Here, we used a silicon photomultiplier and a high-efficiency GAGG crystal to fabricate a compact, battery-powered gamma spectroscopy that can be used in an ocean environment. The developed spectroscopy has compact dimensions of 6.5 × 6.5× 8 cm³ and weighs 560 g. We used LoRa, a low-power wireless protocol for communication. Successful data transmission was achieved within 1.4 m water depth. The developed gamma spectroscopy was able to detect radioactivity from a ¹³⁷Cs point source (3.7 kBq) at a distance of 20 cm in water. Moreover, we demonstrated an unmanned radioactivity monitoring system in a real sea by combining unmanned surface vehicle with the developed gamma spectroscopy. A hidden ¹³⁷Cs source (3.07 MBq) was detected by the unmanned system at a distance of 3 m. After successfully testing the developed mobile spectroscopy in an ocean environment, we believe that our proposed system will be an effective solution for mobile real-time marine radioactivity monitoring.

• Nuclear Engineering and Technology
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• v.54 no.2
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• pp.770-780
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• 2022

In 1993 the University of Extremadura initiated the design, construction and management of the Radiological Alert Network of Extremadura (RAREx). The goal was to acquire reliable near-real-time information on the environmental radiological status in the surroundings of the Almaraz Nuclear Power Plant by measuring, mainly, the ambient dose equivalent. However, the phased development of this network has been carried out from two points of view. Firstly, there has been an increase in the number of stations comprising the network. Secondly, there has been an increase in the number of monitored parameters. As a consequence of the growth of RAREx network, large data volumes are daily generated. To face this big data paradigm, software applications have been developed and implemented in order to maintain the indispensable real-time and efficient performance of the alert network. In this paper, the description of the current status of RAREx network after 30 years of design and performance is showed. Also, the performance of the graphing software for daily assessment of the registered parameters and the automatic on real time warning notification system, which aid with the decision making process and analysis of values of possible radiological and non-radiological alterations, is briefly described in this paper.

• Proceedings of the Korean Radioactive Waste Society Conference
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• 2017.05a
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• pp.379-380
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• 2017

• Nuclear Engineering and Technology
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• v.55 no.11
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• pp.4077-4082
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• 2023

Large areas must be rapidly screened to monitor radiation in marine environments. For this purpose, this study developed a mobile real-time gamma-ray measurement system for shipboard use and evaluated its performance. The system was developed to measure engine or generator cooling water by installing a canister inside the ship. The minimum detectable activity of the system is about 0.8 Bq/L for a 60 s measurement period, and real-time data transmission and remote control are possible. The system was tested in the field and is currently being installed and operated on ships in service. Such a ship-based real-time gamma-radiation measurement system is suitable for a wide range of marine radiation surveillance applications and is expected to be rapidly deployed.

• Nuclear Engineering and Technology
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• v.55 no.12
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• pp.4554-4560
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• 2023

Continuous monitoring of radioactive substances over a prolonged duration can yield crucial insights into the levels of radiation exposure through inhalation, both in the vicinity of nuclear facilities and/or general environments. In this study, we evaluated long-term measurements (2012-2022) of gross alpha-beta activities in the air in the vicinity of nuclear facilities and reference site, distribution characteristics of temporal trends and spatial fluctuations, and factors affecting radioactivity levels. The average airborne gross-α (in mBq m^-3) for onsite and off-site were 0.124 and 0.117, respectively, and the average airborne gross-β (in mBq m^-3) measurements were 1.10 and 1.04, respectively. The activity ratio (AR) of gross-α and gross-β were calculated as a ratio of 0.12. The distribution characteristics of gross-α and gross-β activities in this study area are likely influenced by the meteorological factors and variations in airborne PM concentrations rather than the operation of the nuclear facility.

• Journal of the Korean Geophysical Society
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• v.7 no.1
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• pp.61-72
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• 2004

In this project, under the server-client environment, GIS for the radiological emergency and control system of the vehicles for the environmental radioactivity monitoring was complete. This system is able to display environmental radioactivity data and vehicle's locations through wireless network on real time. Furthermore, it supports not only static analysis function with the collected data regarding nuclear type, collecting time period and vehicle's location but also a documents printing out function.

• Environmental Analysis Health and Toxicology
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• v.1 no.1
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• pp.81-86
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• 1986

After oral administration of $^{14}$ C-labelled $N^{G}$-mono[$^{14}$ C-methyl］-L-arginine into rats, 66.3% of the administered radioactivity has been recovered in the urine, and 86.2% of the total of the recovered radioactivity is recovered in the first 24-hr urine. Distributions of the radioactivity of the acidic, basic, and neutral portions and unmetabolized $N^{G}$-monomethyl-L-arginine are 33.3%, 40.2%, 12.5% , and 0.3%, respectively. The radioactivity corresponding N-monomethylurea is about 50% of the neutral portion and 6% of the administered radioactivity.ity.

• Analytical Science and Technology
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• v.31 no.3
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• pp.134-142
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• 2018

The uranium isotopic ratio in environmental samples around nuclear facilities is important because it reveals information regarding illegal activities or anthropogenic pollution. Determination of uranium isotopes, however, is a challenging task requiring much labor and time because of the complex separation procedures and lengthy process. In this study, a rapid determination method for uranium isotopes in environmental samples was developed using. The sample was completely decomposed using the alkali fusion method. The separation procedure using extraction chromatography (UTEVA) was simplified in a single step without any further removal process for Si and major matrix elements. The established method can be completed within 3 h from sample dissolution to ICP-MS measurement. Most matrix elements and uranium isotopes in the soil samples were well separated and purified. Five types of were used to assess the method's accuracy and precision for a rapid uranium analysis method. The analytical accuracy for all CRM samples ranged from 95.1 % to 97.8 %, and the relative standard deviation was below 3.9 %. From the analytical results, one may draw conclusions that the evaluated method for uranium isotopes using alkali-fusion, the extraction chromatography process, and ICP-MS measurements is fast and fairly reliable owing to its recovering efficiencies. Thus, it is expected that the evaluated method can contribute to the improvement of environmental monitoring ability.

• Journal of Environmental Science International
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• v.15 no.7
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• pp.689-694
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• 2006

To examine inshore radioactive contamination caused by nuclear power plants, nuclear testing, hospital and laboratory, both gross ${\beta}$-radioactivity and ${\upsilon}$-spectrometry were measured. The measurements were taken with the Abalone and Top shell, which had been collected from the four different sites at the coast in Jeju-do (Seongsan, Deajeong, Wimi, Dodu). The activity ranges of concentration were respectively 0.11-0.29 Bq/kg-wet for $^{90}Sr$, 0.01-0.04 Bq/kg-wet for $^{137}Cs$, 36 - 53 Bq/kg-wet for $^{40}K$ in shellfish on the Jeju island. The radioactivities of $^{90}Sr$, $^{137}Cs$ and $^{40}K$ were similar to those in sampling location of shellfish in the coastal on the Jeju island. The radioactivity of $^{90}Sr$ for the Abalone was lower level than that for Top shell. The radio- activity of $^{137}Cs$ for the Abalone was similar to that for the Top shell. But the radioactivity of $^{40}K$ for the Abalone was higher level than that for the Top shell. As a result, the gross ${\beta}$-radioactivity observed was similar to that in nature. Among radionuclides, only $^{90}Sr$, $^{137}Cs$ and $^{40}K$ were detected in a very small amount, and each was also close to the natural levels.

• Analytical Science and Technology
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• v.33 no.4
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• pp.186-196
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• 2020

A simple and rapid preconcentration method of actinide from seawater using Actinide resin was developed and tested with the seawater spiked with a known U and Th. The developed method of Actinide resin based on column chromatography is less time-consuming and requires less labor compared with a typical co-precipitation technique for preconcentration of actinides. U and Th, which are relatively weak-bonded with Actinide resin among actinides, were used to determine the optimum flow rate of seawater sample and evaluate the capacity of Actinide resin to concentrate actinides from seawater. A flow rate of 50 mL min^-1 was available with Actinide resin 2 mL (BV, bed volume). When 5 or 10 L of seawater containing U were loaded on Actinide resin (2 mL, BV) at 50 mL min^-1, the recovery of U was 93 % and 86 %, respectively. For extraction of actinides bound with Actinide resin, we compared three methods: solvent extraction, ashing-acid digestion, and ashing-microwave digestion. Ashing-microwave digestion method shows the best performance of which is the recovery of 100 % for U and 81 % for Th. For the preconcentration of actinides in 200 L of seawater, a typical coprecipitation method requires 2-3 days, but the developed method in this study is achieved the high recovery of actinides within 12 h.