• 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.

• Proceedings of the Korean Nuclear Society Conference
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• 1996.05c
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• pp.535-540
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• 1996

원자로에서 연소되고 나온 사용후핵연료는 영구 처분하기 이전에 대부분 수조(pool)속에 임시로 저장되어 관리되고 있다. 이와 같이 관리되고 있는 사용후핵연료속에 핵폭발 장치로 전용될수 있는 매우 민감한 핵물질인 플루토늄이 다량 포함되어 있기 때문에, 원자력의 평화적 이용·개발을 위한 핵활동의 투명성을 확보하기 위해서는 국가사찰 수행시 현장 적용 가능한 사용후핵연료 검증 기술과 장비를 확보하는 것이 필요하다. 이를 위해 사용후핵연료봉 및 사용후핵연료 집합체 검증을 휘한 고분해능 감마선 분광분석 시스템을 개발하여 현장 테스트를 수행한다. 이를 바탕으로 강화되는 핵비확산 체제와 통제관련 기술의 발전에 대비하고 우리 나라의 국가계량관리체제(SSAC) 확립에 필요한 자체적인 사찰 기술을 개발하여 국가사찰에 적용하는 것이 비파괴측정기술 개발 목적이다.

• Journal of the Korean Magnetics Society
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• v.21 no.1
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• pp.5-9
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• 2011

M$\ddot{o}$ssbauer and Raman spectrum studies have been carried out on the 2b-site Fe ion in the Ba-ferrite (M-type). The thermal dynamics of Fe ion was analyzed by M$\ddot{o}$ssbauer spectra at different angles between the $\gamma$-ray direction and c-axis. The vibration on the 2b-site was more active compare to other direction and had very strong intensity in the Raman spectrum.

• Proceedings of the Korean Vacuum Society Conference
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• 2010.08a
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• pp.68-68
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• 2010

최근에 양전자의 고유 성질을 이용하여 반도체 및 도체의 표면, 계면 그리고 박막의 특성을 분석하는 기술로 소개되고 있다. 양전자는 양의 전하를 갖으며, 반물질인 전자와 쌍소멸하면서 감마선과 Auger 전자를 방출하는 특성을 이용하여 원소의 화학적 분석을 처음으로 증명하였다 (1987, UTA). 이후 도체 및 반도체의 표면 및 박막성장의 초기 성장 양상을 EAES, LEED와 상호보완적으로 활용하여 다양한 결과를 보고한 바 있다. 최근에는 기존의 양전자 이용 Auger전자 분광기의 단점을 극복하고 Time-Of-Flight(TOF) 시스템을 활용하여 향상된 성능과 Cu(100) 표면에서 얻은 전자 스펙트럼의 연구 결과를 소개하고자 한다. UTA의 TOF PAES 시스템을 이용하여 Si(100)표면에 Se 원자의 열적 안정성을 연구하였다. 1ML의 Se을 Si(100)위에 성장한 후 가열하면서 PAES의 스펙트럼을 반복적으로 취하였다. $800^{\circ}C$ 이상의 온도로 가열하는 경우 Se MVV Auger 피크는 약해지고 Si LVV 피크가 나타나기 시작했다. MgO(100) 표면과 Cu2O/ITO 시스템의 온도 안정성 결과를 보고하고 PAES의 향상된 표면 선택도 등 장점이 표면 분석 기술로서 적합함을 보고하고자 한다.

• Journal of Nuclear Fuel Cycle and Waste Technology(JNFCWT)
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• v.16 no.4
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• pp.397-410
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• 2018

When considering the long-term safety assessment of spent-nuclear fuel management, americium is one of the most radio-toxic actinides. Although spectroscopic methods are widely used for the study of actinide chemistry, application of those methods to americium chemistry has been limited. Herein, we purified $^{241}Am$ to obtain a highly pure stock solution required for spectroscopic studies. Quantitative and qualitative analyses of purified $^{241}Am$ were carried out using liquid scintillation counting, and gamma and alpha radiation spectrometry. Highly sensitive absorption spectrometry coupled with a liquid waveguide capillary cell and time-resolved laser fluorescence spectroscopy were employed for the study of Am(III) hydrolysis and oxalate (Ox) complexation. $Am^{3+}$ ions under acidic conditions exhibit maximum absorbance at 503 nm, with a molar absorption coefficient of $424{\pm}8cm^{-1}{\cdot}M^{-1}$. $Am(OH)_3(s)$ colloidal particles formed under near neutral pH conditions were identified by monitoring the absorbance at around 506-507 nm. The formation of ${Am(Ox)_3}^{3-}$ was detected by red-shifts of the absorption and luminescence spectra of 4 and 5 nm, respectively. In addition, considerable enhancements of the luminescence intensities were observed. The luminescence lifetime of ${Am(Ox)_3}^{3-}$ increased from 23 to 56 ns, which indicates that approximately six water molecules are replaced by carboxylate ligands in the inner-sphere of the Am(III). These results suggest that ${Am(Ox)_3}^{3-}$ is formed through the bidentate coordination of the oxalate ligands.

• Journal of the Korean Society of Radiology
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• v.7 no.1
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• pp.31-36
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• 2013

The radioactive gas radon ($^{222}Rn$), which is generated from the decay process of uranium ($^{238}U$) originating from the soil of more than 85 percent higher the porosity of the soil, the soil can radiate out the possibility that many isotopes. In order to protect the human body from radon, above all, the development of accurate measurement techniques to formulate appropriate measures should be followed. This study Gamma-ray spectrometry using a high purity germanium (HPGe) detector, if you want to measure radon unstable the nature radiation of the background problems can be reduced, radium and radon daughter nuclides after radioactive equilibrium leads to Radon concentration was measured, the soil samples from the Gamma-ray emitting nuclides, and the energy spectrum is analyzed.

• Journal of Nuclear Fuel Cycle and Waste Technology(JNFCWT)
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• v.15 no.1
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• pp.35-44
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• 2017

A gamma-ray peak of $^{226}Ra$ (186.2 keV) overlaps with one of $^{235}U$ (185.7 keV) in a gamma-ray spectrometry system. Though reference peaks of $^{235}U$ can be used to correct the peak interference of $^{235}U$ in the analysis of $^{226}Ra$, this requires a complicated calculation process and a high limit of quantitation. On the other hand, evaluating $^{226}Ra$ using the correction constant in the overlapped peak can make a rapid measurement of $^{226}Ra$ without the complicated calculation process as well as overcome the disadvantage in the indirect measurement of $^{214}Bi$, which means the confinement of $^{222}Rn$ gas in a sample container and a time period to recover the secular equilibrium. About 93 samples with 6 species for raw-materials and by-products were prepared to evaluate the activity of $^{226}Ra$ using the correction constant. The results were compared with the activity of $^{214}Bi$, which means the indirect measurement of $^{226}Ra$, to validate the method of the direct measurement of $^{226}Ra$ using the correction constant. The difference between the direct and indirect measurement of $^{226}Ra$ was generally below about ${\pm}20%$. However, in the case of the phospho gypsum, a large error of about 50% was found in the comparison results, which indicates the disequilibrium between $^{238}U$ and $^{226}Ra$ in the materials. Application results of the contribution ratio of $^{226}Ra$ were below about ${\pm}10%$. The direct measurement of $^{226}Ra$ using the correction constant can be an effective method for its rapid measurement of raw materials and by-products because the activity of $^{226}Ra$ can be produced with a simple calculation without the consideration of the integrity of a sample container and the time period to recover the secular equilibrium.

• Analytical Science and Technology
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• v.16 no.5
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• pp.391-398
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• 2003

Basic research for the determination of boron content in biological sample has been carried out using the PGAA facility of the 24MW research reactor(HANARO). For investigation of characteristics for the measurement condition, neutron flux and its homogeneity were measured at irradiating geometry. The size of thermal neutron beam collimated from beam guide is $2{\times}2cm^2$ at the sample position. The neutron flux measured was the range of $1.0{\sim}6.5{\times}10^7n{\cdot}cm^{-2}{\cdot}s^{-1}$, and flux distribution from center within the radius of 4.5 mm and 9.0 mm was $5.77{\pm}0.71{\times}10^7n{\cdot}cm^{-2}{\cdot}s^{-1}$ and $4.68{\pm}1.64{\times}10^7n{\cdot}cm^{-2}{\cdot}s^{-1}$, respectively. Accordingly, sample size is adjusted within 10 mm for a homogeneous irradiation of high quality. Measurement system is designed to reduce the background source by Compton scattering and to improve the analytical sensitivity. To investigate the energy calibration and Compton suppression effect of gamma-ray counting system, the background conditions on both of Compton and single-mode were measured using NaCl standard. On the other hand, degree of spectral interference for sodium 472 keV peak as a matrix effect in the sample is established for an accurate boron analysis, and then boron content in three certified reference materials (NIST SRM 1570a, 1547, 1573a) was measured by using two modes and the results were compared with each other.

• Proceedings of the Korean Vacuum Society Conference
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• 2012.08a
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• pp.237-237
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• 2012

토파즈는 Al2SiO4 ((F,OH)2) 화학성분을 이루고 있는 광물로써 주로 Fe, Cr, V 등과 같은 불순물을 포함하고 있다. 토파즈는 colorless, blue, pink, yellow 등 다양한 컬러로 산출된다. 결정 내 Si4+ 가 있어야 할 자리에 Al3+ 가 치환되면 Al3+ 를 둘러싸고 있는 4개의 산소 중 하나의 최외각 전자가 전자가를 맞추기 위해 주변에 있던 수소와 결합하여 hole center를 형성한다. 이때 토파즈는 옅은 황색의 컬러를 발색하게 된다. 그 외 청색과 핑크색 등의 컬러는 Al3+ 자리에 치환된 Fe, Cr 등과 같은 불순물에 의해 발색을 일으킨다. 또한 토파즈는 인위적으로 감마선, 전자 빔, 양성자 빔, 중성자 빔을 통해서도 hole center를 형성시켜 컬러를 발색시킬 수 있다고 잘 알려져 있다. 본 연구에서는 총 8개의 무색 토파즈를 이용하여 다양한 조건(energy 및 dose)의 전자 빔 조사를 통해 각 조건 별 컬러변화 및 분광학적 특성변화를 관찰하였다. 모든 시료는 WD-XRF를 통해 정성분석을 하였고, 전자스핀공명(ESR)기기를 통해 전자 빔 조사 전과 후 전자의 스핀 특성 변화를 관찰하였다. 자외선-가시광선 분광분석결과 모든 시료는 전자빔 조사 후 황색과 관련이 있는 450 nm 부근의 파장 영역에서 흡수 peak가 증가하는 것을 확인할 수 있었다. 또한 전자 빔 조사 후 전자스핀공명 분석 결과에서도 Fe3+ 와 관련이 있는 g=3.5~4 영역은 감소하는 반면에 hole center와 관련이 있는 g=2.012 영역이 증가하는 향상을 보였다. 본 연구결과를 통해 우리는 전자 빔 조사 조건에 따라 토파즈의 결정 내부에 미치는 영향 및 컬러 변화와의 상관관계에 대해 확인할 수 있었다.

• Journal of the Korean Chemical Society
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• v.21 no.6
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• pp.427-433
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• 1977

A neutron activation method has been developed for the simultaneous determination of chromium, iron, lanthanum, scandium and zinc in river-water samples. The sample is sealed in the silica ampoule without pretreatment and irradiated for a week at a thermal neutron flux of $1{\times}10^{13}n{\cdot}cm^{-2}{\cdot}sec^{-1}$. After cooling for about two days, the elements in the sample are sequentially extracted at different pH by 0.1M oxine-chloroform solution. The organic layers are checked by Gamma-ray spectrometry with $″3\;{\times}\;3″$ NaI (T1) detector connected to a 800-channel pulse hight analyzer. The ppb concentration of the elements in most of river-water samples could be determined by this method. The tracer study for the quantitative separation of the elements was also carried out.