• Economic and Environmental Geology
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• v.40 no.4
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• pp.389-401
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• 2007

The oxygen and hydrogen isotopic composition in precipitation, groundwater and geothermal water were monitored over four-year period from 2001 to 2004 at the Yuseong catchment, Daejeon. By analyzing the long term rainfall pattern, we found out the drought cycle of 6 or 7 year. We fortunately revealed that the oxygen and hydrogen isotopic composition of rain has progressively changed to heavier isotopic ratios from 2001 to 2004. The weighted mean values of ${\delta}^{18}O\;and\;{\delta}D$ of rain are calculated to be $-7.7%o\;and\;-51%o$, respectively. These isotopic values are much heavier than those of groundwater and geothermal water collected at the same period, which indicates that the rain or snow of the study area would not immediately affect the isotopic composition of groundwater or geothermal water. Comparing with the previous data, the groundwater and geothermal water collected at 1990 and 1992 year has the heaviest isotopic composition and afterwards their isotopic composition has been progressively shifted to the direction of lighter composition field.

• Analytical Science and Technology
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• v.8 no.4
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• pp.477-480
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• 1995

Isotopic-spectral method [I] was applicated for determination of carbon in silicate materials (pure silica, guartz glasses, geological probs etc.). Isotopic heterogeneous balancing of carbon in gaseous phase and solid samples was carried out at the temperature of $1500-1900^{\circ}K$. Spectroscopic measuring of isotope concentration in a balanced gas was made using the electron-vibrational band heads of CO molecules excited in HF discharge. Limits of detection of carbon concentrations appear to be $n^*10^{-6}$.

• Proceedings of the Korea Water Resources Association Conference
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• 2005.05b
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• pp.29-38
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• 2005

It is important to understand groundwater conditions such as recharge, flow and hydrochemical process occurred within an aquifer for groundwater protection and groundwater resource management. Groundwater from the Triassic Sherwood Sandstone aquifer of North Yorkshire has been used for industrial purposes and domestic water supply. Tn order to understand the processes affecting groundwater chemistry and identify the sources of high chloride, sulphate and nitrate concentrations hydrochemical and isotopic measurements were carried out. Hydrochemical and isotopic measurements indicated that five groundwater types exist within the Sherwood Sandstone aquifer of study area. The results of hydrochemical and isotopic measurements showed that older groundwaters have different hydrochemical and isotopic characteristics from recent recharge water. It was also found that water-rock interactions are the dominant mechanism controlling the ${\delta}^{13}C$ composition of dissolved inorganic carbon, the ${\delta}^{34}S\;and\;{\delta}^{18}O$ composition of dissolved sulphate and the strontium isotope ratios ($^{87}Sr/^{86}Sr$) in recent recharge water and old groundwater. Several abstraction boreholes within the Selby wellfield have been contaminated by saline water. The isotopic data of saline groundwater samples taken from these abstraction boreholes indicate that saline waters are derived from the dissolution of the Triassic evaporites within the Mercia Mudstone.

• Economic and Environmental Geology
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• v.13 no.1
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• pp.21-27
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• 1980

${\delta}^{13}C$ and ${\delta}^{18}O$ values were determined for the Paleozoic limestones (Great Linestone Series) from the Taebaegsan region and the age-unknown limestones (Janggun Formation) from the Janggun mine, Korea. Limestones of the Great Limestone Series exhibit a range of carbon isotopic composition from -4.5 +1.3‰ with a mean ${\delta}^{13}C$ value of -1.1‰, relative to the PDB standard, and of oxygen isotpic composition from +8.8 to +23.3‰ with a mean ${\delta}^{18}O$ value of +16.0‰, relative to the SMOW, falling into the normal marine limestone range according to Keith and Weber (1964), and Degens and Epstein(1964). Carbon isotopic composition of limestones of the Great Limestone Series becomes progressively lighter from Pungchon limestone of middle Cambrian age to mid-Ordovician Maggol limestone, possibly due to change in depositional environment in the Taebaegsan basin. Variation in isotopic composition of limestones from Hwajeol to Dumugal formation offers the possibility or deposition in shallow sea environment, in which fresh waters were added in several stages. Janggun limestone of unknown age may be corelated with the Paleozoic limestones of Great Limestone Series as infered from the istopic composition ranging from -2.8 to + 0.7‰ of ${\delta}^{13}C$ and +13.4 to +22.4‰ of ${\delta}^{18}O$.

• Journal of the Korean earth science society
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• v.35 no.2
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• pp.97-103
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• 2014

An isotopic hydrograph separation technique has been able to determine the contribution of new water (event water such as rain or snowmelt) and old water (pre-event water like groundwater) to a stream hydrograph for last several decades using stable water isotopes. It is based on the assumption that the isotopic compositions of both new water and old water at a given instant in time are known and the stream water is a mixture of the two waters. In this study, we show that there is a systematic error (standard error in the new water fraction) in the isotopic hydrograph separation if the average isotopic compositions of new water were used ignoring the temporal variations of those of new water. The standard error in the new water fraction is caused by: (1) the isotopic difference between the average value and temporal variations of new water; (2) the new water fraction as runoff contributing to the stream during rainfall or spring melt; and (3) the isotopic differences between new and old water (inversely). The standard error is large, in particular, when new water dominates the stream flow, such as runoff during intense rainfall and in areas of low infiltration during spring melt. To reduce the error in the isotopic hydrograph separation, incorporation of fractionation in the isotopic composition of new water observed at a point should be considered with simultaneous sampling of new water, old water and stream water.

• Nuclear Engineering and Technology
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• v.52 no.6
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• pp.1148-1155
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• 2020

This work presents two different methods for quantifying and propagating the uncertainty associated with fuel composition at end of life for cask criticality calculations. The first approach, the computational approach uses parametric uncertainty including those associated with nuclear data, fuel geometry, material composition, and plant operation to perform forward depletion on Monte-Carlo sampled inputs. These uncertainties are based on experimental and prior experience in criticality safety. The second approach, the data-driven approach relies on using radiochemcial assay data to derive code bias information. The code bias data is used to perturb the isotopic inventory in the data-driven approach. For both approaches, the uncertainty in k_eff for the cask is propagated by performing forward criticality calculations on sampled inputs using the distributions obtained from each approach. It is found that the data driven approach yielded a higher uncertainty than the computational approach by about 500 pcm. An exploration is also done to see if considering correlation between isotopes at end of life affects k_eff uncertainty, and the results demonstrate an effect of about 100 pcm.

• Proceedings of the Korean Nuclear Society Conference
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• 1998.10a
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• pp.317-317
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• 1998

• Nuclear Engineering and Technology
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• v.47 no.7
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• pp.924-933
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• 2015

The correlation of the isotopic composition of uranium, plutonium, neodymium, and cesium with the burnup for high burnup pressurized water reactor fuels irradiated in nuclear power reactors has been experimentally investigated. The total burnup was determined by Nd-148 and the fractional $^{235}U$ burnup was determined by U and Pu mass spectrometric methods. The isotopic compositions of U, Pu, Nd, and Cs after their separation from the irradiated fuel samples were measured using thermal ionization mass spectrometry. The contents of these elements in the irradiated fuel were determined through an isotope dilution mass spectrometric method using $^{233}U$, $^{242}Pu$, $^{150}Nd$, and $^{133}Cs$ as spikes. The activity ratios of Cs isotopes in the fuel samples were determined using gamma-ray spectrometry. The content of each element and its isotopic compositions in the irradiated fuel were expressed by their correlation with the total and fractional burnup, burnup parameters, and the isotopic compositions of different elements. The results obtained from the experimental methods were compared with those calculated using the ORIGEN-S code.

• Proceedings of the Mineralogical Society of Korea Conference
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• 2001.06a
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• pp.75-75
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• 2001

We report Sr, Nd and Pb isotope data of clinopyroxene separates from ultramafic xenoliths and their host basaltic rocks in Jeju Island, Baekryeong Island, Boeun and Ganseong, Korea. The isotopic data of the xenoliths and host basalts are distinctly different from those of Korean basement rocks. Except for two xenoliths from Ganseong, all samples in this study have isotopic ratios within the combined range of MORB-OIB data. All basaltic rocks have Nd-Sr-Pb isotope compositions different from those of xenoliths, indicating that the host basaltic magma did not derive from the lithospheric mantle where the xenoliths originated. The range of isotopic composition of xenoliths is much greater than that observed in host basalts, which reflects small-scale heterogeneity of the lithospheric mantle. The greater isotopic heterogeneity of the lithospheric mantle probably reflects its long-term stability. The spinel peridotite xenolith data of Jeju Island, Baekryeong Island and Boeun display mixing hyperbolas between DMM and EM II end members. Since Jeju basalts have EM II-like isotopic signature, the mixing relationship shown by the isotopic data of the Jeju xenoliths can be interpreted as the result of infiltration of metasomatic fluid or melt derived from basaltic magma into DMM-like lithospheric mantle. In contrast to other xenolith sites, the Ganseong xenoliths are dominantly clinopyroxene megacryst and pyroxenite. Clinopyroxene megacrysts have different isotopic ratios from their host basalt, reflecting its exotic origin. Two Ganseong xenoliths (wherlite and clinopyroxenite) have much enriched Sr and Nd isotopic ratios and Nd model ages of 2.5-2.9 Ga, and plot in an array away from the MORB-OIB field. The mantle xenoliths from Korean Peninsula have similar $\^$87/Sr/$\^$86/Sr,$\^$143/Nd/$\^$144/Nd and $\^$207/Pb/$\^$204/Pb ratios to, but higher $\^$208/Pb/$\^$204/Pb ratios than, those from eastern China, indicating that Korean xenoliths are derived from the lithospheric mantle with higher Th/U ratio compared with Chinese ones. The isotopic data of xenolith-bearing basalts of Baekryeong Island and Ganseong, along with Ulreung and Dok Islands, show a mixing trend betlveen DMM and EM I in Sr-Nd-Pb isotopic correlation diagrams, which is also observed in tile northeastern Chinese basalts. However, the Jeju volcanic rocks show an EM II signature that is observed in southeastern Chinese basalts. The isotopic variations in volcanic rocks from the northern and southern portions of the East Asia reflect a large-scale isotopic heterogeneity in their source mantle.

• 한국해양학회지
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• v.24 no.2
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• pp.69-78
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• 1989

Cultivated pearls, composed of aragonite crystals, show two distinctive layers: nacreous and conchiolin organic layers. Each aragonite crystal is surrounded by organic matrix, which probably consists of amino acids. Nucleus, surrounded by pearl layer, also consists of nacreous crystals, suggesting that there is a close mineralogical and ultrasturctural relationship between pearl and nucleus. Carbon isotopic values of cultivated pearls are within the range of marine carbonate carbon. Oxygen isotopic composition indicates that the temperature for the growth of pearl and pearl oyster ranges from 16.4 to $21.4^{\circ}C$ and from 15.5 to $24.8^{\circ}C$, corresponding to the summer temperature range of the cultivating area. Elemental composition of pearl, pearl oyster, and nucleus shows that there is a difference in chemical composition depending upon the original mineralogy and the chemical composition of water in which shells grow. Especially, a strong relationship exists between pearl and the inner layer of pearl oyster because both are composed of nacreous aragonite and formed in a shallow marine environment.