• Bulletin of the Korean Chemical Society
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• 제23권5호
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• pp.727-735
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• 2002

Proton coupled carbon-13 relaxation experiment was performed to investigate the effect of vicinal protons on spin-lattice relaxation of methylene carbon-13 in n-undecane. A BIRD type pulse sequence was employed as a way to check the validity of describing the 13CH2 moiety as an isolated AX2 spin system. The results show that the presence of vicinal protons exerts substantial influence on the relaxation of methylene carbon-13, indicating that it is not a very good approximation to treat a methylene moiety as an isolated AX2 spin system.

• 핵의학기술
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• 제15권1호
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• pp.86-89
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• 2011

최근 들어 양전자방출단층촬영(positron emission tomography, PET) 대표적인 진단검사인 FDG (2-[$^{18}F$]fluoro-2-deoxy-D-glucose)를 이용한 전신암 및 장기별 대사 검사뿐만 아니라 또 다른 양전자 방출 동위원소 탄소-11로 표지 된 다양한 방사성의약품 사용이 증가될 예정이다. 본 논문에서는 현재 국내에 설치 보급되어있는 국산 KOTRON-13 사이클로트론에 냉각 성능이 개선된 탄소-11 표적 장치를 설계, 제작하고, 다양한 생산시험을 통하여 탄소-11의 생산량 증대를 입증 하였다. 성공적으로 기존의 불소-18 타겟과 새로운 탄소-11 타겟 호환장치를 도입하였고, 실험 결과 고효율 탄소-11표적 장치가 내수성이 우수하고, 30분 조사 시 최대 2,000 mCi를 생산하였다. 본 시험결과를 통해 향후 불소-18만이 생산 가능했던 국산 KOTRON-13 사이클로트론에 효율적이고 안정적으로 탄소-11생산 시스템을 도입할 수 있음을 증빙하였다.

• 한국광물학회지
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• 제24권4호
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• pp.289-300
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• 2011

규산염 물질의 탄소 용해도에 대한 미시적 연구는 규산염 물질의 성질 변화와 지구 시스템 진화에 탄소가 미치는 영향의 이해에 매우 중요하다. 본 연구에서는 탄소가 용해된 엔스테타이트 시료에 대하여 라만(Raman) 분광분석을 실시하고, 양자 화학 계산을 통해 결정구조 내에 용해된 탄소의 원자 환경과 핵자기공명 분광 특성을 예측하였다. 1.5 GPa $1,400^{\circ}C$의 온도 압력 조건에서 2.4 wt%의 비정질 탄소와 함께 합성한 엔스테타이트의 라만 실험에서 엔스테타이트의 진동양상은 확인할 수 있었으나, $CO_2$나 탄산염 이온의 진동양상에 대한 정보는 획득하지 못하였다. 이는 엔스테타이트 내에 용해된 탄소의 양이 매우 적어 시료를 구성하는 원자들의 집합적인 진동양상을 측정하는 라만 분광분석으로는 검출이 어려움을 지시한다. 특정 핵종 중심의 핵자기공명 분광분석을 이용하면, 구조 내에 존재하는 탄소만 선택적으로 측정할 수 있다. 특히 $^{13}C$ NMR 화학 이동(chemical shift)은 원자 환경에 따라 민감하게 변하므로, 양자 화학 계산을 이용하여 $CO_2$와 C가 치환된 엔스테타이트 클러스터의 $^{13}C$ NMR 화학 차폐 텐서(chemical shielding tensor)를 계산하였다. 계산 결과 $CO_2$의 피크는 125 ppm에서 나타나며 이는 기존의 실험결과와 일치하며, 상압에서는 생성이 어렵지만 고압환경에서 생성될 가능성이 있는 배위수가 4인 C의 화학 이동 값은 ~254 ppm으로 예측되었다. 이와 같은 양자 화학 계산 결과는 고분해능 $^{13}C$ NMR 실험의 이해를 돕고 탄소의 원자 환경을 연구하는데 도움을 줄 것이다.

• 분석과학
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• 제13권4호
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• pp.539-543
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• 2000

The quantitative aspects of 2D carbon-13 INADEQUATE (Incredible Natural Abundance DoublE QUAntum Transfer Experiment) experiment were studied on the basis of the time needed in various concentrations of samples. In order to evaluate the quantitative time of this experiment, eight compounds were selected (M. W. ca. 150-500). The effect on time needed of various concentrations showed exponential decay function, Y=$8.15X^{-0.64}$.

• Proceedings of the National Institute of Ecology of the Republic of Korea
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• 제2권4호
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• pp.259-273
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• 2021

We conducted a study to investigate the characteristics of the carbon cycle of two streams (located in Shig a Prefecture, Japan), having similar size, namely, the Adokawa stream (length: 52 km, area: 305 km², watershed population: 8,000) and the Yasukawa stream (length: 62 km, area: 380 km², watershed population: 120,000), but with different degree of human activity. Samples were collected from these two streams at 14 (Adokawa stream) and 23 (Yasukawa stream) stations in the flowing direction. The dissolved inorganic carbon (DIC) concentration and the stable carbon isotope ratio of DIC (δ¹³C-DIC) were measured in addition to the watershed features and the chemical variables of the stream water. The δ¹³C-DIC (-9.50 ± 2.54‰), DIC concentration (249 ± 76 µM), and electric conductivity (52 ± 13 µS/cm) in Adokawa stream showed small variations from upstream to downstream. However, the δ¹³C-DIC (-8.68 ± 2.3‰) upstream of Yasukawa stream was similar to that of Adokawa stream and decreased downstream (-12.13 ± 0.43‰). DIC concentration (upstream: 272 ± 89 µM, downstream: 690 ± 37 µM) and electric conductivity (upstream: 69 ± 17 µS/cm, downstream: 193 ± 37 µS/cm) were higher downstream than upstream of Yasukawa stream. The DIC concentration of Yasukawa stream was significantly correlated with watershed environmental variables, such as, watershed population density (r = 0.8581, p<0.0001, n = 23), and forest area percentage of the watershed (r = -0.9188, p<0.0001, n = 23). δ¹³C-DIC showed significant negative correlation with the DIC concentration (r = -0.7734, p<0.0001, n = 23), electric conductivity (r = -0.5396, p = 0.0079, n = 23), and watershed population density (r = -0.6836, p = 0.0003, n = 23). Our approach using a stable carbon isotope ratio suggests that DIC concentration and δ¹³C-DIC could be used as indicators for monitoring the health of stream ecosystems with different watershed characteristics.

• Bulletin of the Korean Chemical Society
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• 제21권11호
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• pp.1077-1084
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• 2000

The dipolar effect of neighboring protons that are not directly bonded to the carbon of interest on coupled carbon-13 relaxation in a simple organic molecule has been studied by comparing the relaxation behaviors of labeled carbon-13 in $Br13CH_2COOH$ with those in $BrCH_213COOH.$ Various pulse sequences, such as coupled inversion recovery pulse sequence, J-negative and J-positive pulse sequence, and nonselective and selective proton ${\pi}pulse$ sequence, were employed to perform the required coupled spin relaxation experiments. To gain information on various spectral densities, including that of dipolar-CSA cross correlation, the experiments were performed on two different spectrometers, operating, respectively, at 50.31 and 125.51MHz for 13C. The magnitude of CH dipolar spectral densities for $BrCH_213COOH$ was found to be about 8% of those for $Br13CH_2COOH$, which means the effect due to the protons not directly bonded to the carbon of interest is small but not completely negligible.

• Bulletin of the Korean Chemical Society
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• 제13권6호
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• pp.595-599
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• 1992

The temperature dependence of C-13 chemical shifts are observed for the cyclooctanone arylhydrazones. The temperature-dependent chemical shifts for these derivatives are explained by postualating the existence of two equilibrating structures. In addition, the assignment between the $^{13}C$ signals of methylene carbon pairs can be done by application of the ${gamma}$ -substituent effect.

• Bulletin of the Korean Chemical Society
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• 제8권2호
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• pp.73-79
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• 1987

In this work we have investigated temperature dependence of spin-rotational relaxation rate, $(1/T_1)_{SR}$, of methyl carbon-13's in 2-bromo-p-xylene, 2,5-dimethylaniline, and 2,5-dimethylanisole and have found that temperature behaviors of two methyl carbon-13's in ortho- and meta-position, respectively, are substantially different. It has been confirmed that the modified Burke-Chan model proposed by Park et al. can nicely explain different temperature dependence of $(1/T_1)_{SR}$ for these two methyl carbon-13's while the original Burke-Chan model fails to do so.

• 한국환경과학회지
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• 제5권4호
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• pp.429-440
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• 1996

A global carbon cycle model (GCCM), that incorporates interaction among the terrestrial biosphere, ocean, and atmosphere, was developed to study the carbon cycling aid global carbon budget, especially due to anthropogenic $CO_2$ emission. The model that is based on C, 13C and 14C mass balance, was calibrated with the observed $CO_2$ concentration, $\delta$13C and $\Delta$14C in the atmosphere, Δ14C in the soil, and $\Delta$14C in the ocean. Also, GCCM was constrained by the literature values of oceanic carbon uptake and CO, emissions from deforestation. Inputs (forcing functions in the model) were the C, 13C and 14C as $CO_2$ emissions from fossil fuel use, and 14C injection into the stratosphere by bomb-tests. The simulated annual carbon budget of 1980s due to anthropoRenic $CO_2$ shows that the global sources were 5.43 Gt-C/yr from fossil fuel use and 0.91 Gt-C/yr from deforestation, and the sinks were 3.29 Gt-C/yr in the atmosphere, 0.90 Gt-C/yr in the terrestrial biosphere and 2.15 Gt-C/yr in the ocean. The terrestrial biosphere is currently at zero net exchange with the atmosphere, but carbon is lost cia organic carbon runoff to the ocean. The model could be utilized for a variety of studies in $CO_2$ policy and management, climate modeling, $CO_2$ impacts, and crop models.

• Carbon letters
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• 제13권2호
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• pp.94-98
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• 2012

Herein, macroporous carbon foams were successfully prepared with phenol and formaldehyde as carbon precursors and an ionic liquid, 1-butyl-3-methylimidazolium hexafluorophosphate ($BMIPF_6$), as a pore generator by employing a polymerization-induced phase separation method. During the polycondensation reaction of phenol and formaldehyde, $BMIPF_6$ forms a clustered structure which in turn yields macropores upon carbonization. The morphology, pore structure, electrical conductivity of carbon foams were investigated in terms of the amount of the ionic liquid. The as-prepared macroporous carbon foams had around 100-150 ${\mu}m$-sized pores. More importantly, the electrical conductivity of the carbon foams was linearly improved by the addition of $BMIPF_6$. To the best of the author's knowledge, this is the first result reporting the possibility of the use of an ionic liquid to prepare porous carbon materials.