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방사성폐기물 시료 중 $\^{241}$Am과 $\^{244}$Cm의 정량
조기수,김태현,전영신,지광용,김원호,Joe Kih Soo,Kim Tae Hyun,Jeon Young Shin,Jee Kwsng Yong,Kim Won Ho 한국방사성폐기물학회 2005 방사성폐기물학회지 Vol.3 No.1
Anion exchange chromatography and HDEHP extraction chromatography using DTPA-lactic acid as an eluent were applied in series for the separation of $^{241}$Am and $^{244}$Cm in radwaste samples. The separated elements were determined by electrodeposition at the sodium hydrogen sulfate-sodium sulfate buffer solution followed by alpha-spectrometry. The recovery yields of $^{241}$Am and $^{244}$Cm were 85.2$\pm$$15.3\%$, respectively, from the synthetic solution of spent nuclear fuel sample. The amounts of 241Am and 2440m determined in radwaste sample solutions of condensate bottoms were at the range of 1.5-1.9 Bq/g and -1.7 Bq/g, respectively.
알파분광분석법에 의한 $^{237}Np$ 정량 및 사용후핵연료 시료에의 적용
조기수,김정석,한선호,박영재,김원호,Joe Kih-Soo,Kim Jung-Suck,Han Sun-Ho,Park Yeong-Jai,Kim Won-Ho 한국방사성폐기물학회 2006 방사성폐기물학회지 Vol.4 No.2
Alpha spectrometry was studied for the determination of $^{237}Np$ in spent nuclear fuel samples. The optimum condition for the electrodeposition of $^{237}Np$ was obtained as follows : for $1{\sim}1.5$ hour of deposition time, at the current intensity of $1.2{\sim}1.5$ A and at sodium sulfate electrolyte without organic additive. The deposition yield and its reproducibility on $^{237}Np$ was decreased as the amount of $^{237}Np$ decreased from 4.16 Bq down to 0.0264 Bq(1ng). The recovery yield of $^{237}Np$ determined by alpha spectrometry after separation in synthetic solution was $98.8{\pm}5.1%$(n=4). The contents of $^{237}Np$ in spent nuclear fuel samples were determined and the result showed an agreement within 10% of a difference between the measurement and the calculation.
조기수,엄태윤,김승수,김연두,Kih Soo Joe,Tae Yoon Eom,Seung Soo Kim,Youn Doo Kim 대한화학회 1988 대한화학회지 Vol.32 No.5
PRP-1 역상 충전제에 Cetylpyridinium Chloride를 흡착한 흡착분리관과 Tetrabutylammonium을 이온상호작용제로 사용하는 동적계에서 $BF_4^{-1}$를 포함하는 무기음이온들의 크기인자(k')를 측정하였다. 용리액의 농도, pH변화에 따라 이들 이온들의 분리조건을 검토한 후 폐기물 시료중 붕소정량에 적용하였다 Capacity factors (k') of some inorganic anions including $BF_4^{-1}$ were measured on cetylpyridinium coated column, and with dynamic system using tetrabutylammonium salicylate on PRP-1 reversed-phase column, respectively. After optimum separation condition was obtained this method was applied to the determination of boron in some different type samples.
이온크로마토그래피에 의한 $PuO_2^{2+}$, $Pu^{4+}$ 및 $Pu^{3+}$의 분리
조기수,김종구,박양순,김도양,엄태윤,Joe, Kih Soo,Kim, Jong Gu,Park, Yang Soon,Kim, Do Yang,Eom, Tae Yoon 대한화학회 1999 대한화학회지 Vol.43 No.3
이온크로마토그래피를 이용하여 Pu 화학종의 분리방법을 검토하였다. 환원제(KI, $NaNO_2$) 또는 산화제(KBrO_3$)를 사용하여 Pu의 산화수를 조절한 후 1-octanesulfonate 와 ${\alpha}$-HiBA 용리액을 사용하는 동적계에서 $PuO_2^{2+},\; PC^{4+}$ 및 $Pu^{3+}$의 화학종을 각각 안정하게 개별분리하였다. Iodide와 nitrite를 동시에 사용하여 Pu 화학종들을 $Pu^{3+}$까지 환원한 다음 이온크로마토그래피로 안정하게 분리하였다. Separation of plutonium species was studied by ion chromatography installed in a glove box for the determination of plutonium element. The plutonium species, $PuO_2^{2+},\; PC^{4+}\; and\; Pu^{3+}$, were stably separated on dynamically equilibrated cation exchanger using 1-octanesulfonate and ${\alpha}$-HiBA eluant after controlling the plutonium oxidation states with KI, $NaNO_2\;or=;KBrO_3$ based on the oxidation-reduction potentials. For the separation of plutonium from other matrix, $PuO_2^{2+}\; and\; Pu^{4+}$ were reduced to $Pu^{3+}$ with KI and $NaNO_2$ followed by cation exchange chromatography.
Germanium(Ⅳ)-Morin 착물에 대한 네모파 양극벗김 전압전류법적 연구
손세철,박용준,조기수,Sohn, Se Chul,Park, Yong Joon,Joe, Kih Soo 대한화학회 1997 대한화학회지 Vol.41 No.11
Germanium(IV)-Morin 착물에 대한 네모파 양극벗김 전압전류법적 연구를 0.5 M 황산 지지전해질에서 수행하였다. Germanium(IV)-Morin 착물의 피크전위는 - 0.606 V vs. Ag/AgCl에서 나타났다. Germanium(IV)-Morin 착물의 피크전류 크기에 미치는 지지전해질의 황산 농도, Morin의 농도, 축적전위 및 축적시간의 의존성 등에 대하여 논의하였다. 또한, Germanium(IV)-Morin 착물의 피크전류 크기에 영향을 주는 금속 양이온들의 방해효과도 조사하였다. 이 방법을 적용시켜 축적시간을 60초로 하였을 때 Germanium(IV)의 검출한계는 $3.76{\times}10^{-7}M(27 {\mu}g/L)$ 이었으며, 0.4 mg/L($5.5{\times}10^{-6}$ M)의 Germanium(IV) 분석에 대한 상대표준편차(n=8)는 3.2% 이었다. Square-wave anodic stripping voltammetry was applied to the germanium(IV)- Morin complex in 0.5 M sulfuric acid as a supporting electrolyte. The peak potential appeared at - 0.606 V vs. Ag/AgCl. Effects of sulfuric acid concentration, Morin concentration, accumulation potential, and accumulation time on the stripping peak current for the complex of germanium(IV)-Morin were studied. Interferences by other metal cations that affect on stripping peak current were also investigated. The detection limit was found to be $3.76{\times}10^{-7}M(27 {\mu}g/L)$ for germanium(IV) using 60 seconds of accumulation time. The relative standard deviation (n=8) for 0.4 mg/L($5.5{\times}10^{-6}$ M) germanium(IV) was 3.2%.