• Proceedings of the Petrological Society of Korea Conference
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• 2006.05a
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• pp.42-44
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• 2006

• Analytical Science and Technology
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• v.17 no.5
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• pp.388-392
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• 2004

Structural studies of membrane proteins, importantly involving interpretation of genomics information, many signaling pathway and major drug target for drug discovery, are having difficulty in characterizing the function using conventional solution nmr spectroscopy and x-ray crystallography because phospholipid bilayers hindered fast tumbling and crystallization. Here, we studied the structure of the pf1 coat protein in oriented phospholipid bilayers by home-built solid-state NMR probe. Bacteriophage pf1 was purified from Paeudomonas Aeruginosa and coat protein of bacteriophage pf1 was isolated from DNA and other proteins.

• Analytical Science and Technology
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• v.12 no.3
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• pp.184-189
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• 1999

$^{51}V$ NMR and cyclic voltammetry studies on the interaction of vanadate and N-benzyliminodiacetate (Bz-IDA) in aqueous solution have been studied. From the NMR spectra two $^{51}V$ NMR peaks resulting at -515.5 and -500.1 ppm, due to the complexations between vanadate(V) and Bz-IDA at pH 5. has been observed. From the cyclic voltammograms the reduction-oxidation of the vanadate(V) complex has been found to be one-electron reaction.

• Rubber Technology
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• v.20 no.4
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• pp.249-262
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• 2019

• Proceedings of the Petrological Society of Korea Conference
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• 2009.05a
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• pp.29-31
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• 2009

• 한국신재생에너지학회:학술대회논문집
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• 2005.06a
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• pp.660-662
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• 2005

본 연구에서는 미 인근 해저에서 ODP로 확인된 부존 하이드레이트 샘플을 다양한 분광학 및 실험적 분석 방법을 통해 시료의 물성 및 특성을 파악하여 부존된 하이드레이트 자원의 성분 파악을 목적으로 하고 있다. 일반적으로 가스 하이드레이트 연구에 있어서 X-ray diffractometer, NMR stectrometer, Raman spectrometer 등 분광학적 분석기기를 이용하여 가스 하이드레이트의 구조 및 성분을 규명한다. 본 연구에서는 실험실에서 인위적으로 만들어진 메탄 하이드레이트와 심해저 천연가스 하이드레이트 층에서 채취된 샘플의 비교 분석을 통하여 심해에 매장되어 있는 천연가스 하이드레이트의 구조 및 성분을 규명하였다 XRD 결과로부터 천연가스 하이드레이트는 sI의 구조를 가지며 NMR 및 Raman 결과에 의하면 하이드레이트 내에 포집되어 있는 가스의 주 성분은 메탄인 것으로 밝혀졌다. 또한 천연가스 하이드레이트를 이용한 이산화탄소의 치환 실험을 통하여 심해저 천연가스 하이드레이트 층의 이산화탄소 저장 매체로의 활용 가능성을 조사하였다.

• Journal of the Mineralogical Society of Korea
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• v.24 no.4
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• pp.301-312
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• 2011

The study on the atomic structure of iron-bearing silicate glasses has significant geological implications for both diverse igneous processes on Earth surface and ultra-low velocity zones at the core-mantle boundary. Here, we report experimental results on the effect of iron content on the atomic structure in iron-bearing alkali silicate glasses ($Na_2O-Fe_2O_3-SiO_2$ glasses, up to 16.07 wt% $Fe_2O_3$) using $^{29}Si$ and $^{17}O$ solid-state NMR spectroscopy. $^{29}Si$ spin-lattice ($T_1$) relaxation time for the glasses decreases with increasing iron content due to an enhanced interaction between nuclear spin and unpaired electron in iron. $^{29}Si$ MAS NMR spectra for the glasses show a decrease in signal intensity and an increase in peak width with increasing iron content. However, the heterogeneous peak broa-dening in $^{29}Si$ MAS NMR spectra suggests the heterogeneous distribution of $Q^n$ species around iron in iron-bearing silicate glasses. While nonbridging oxygen ($Na-O-Si$) and bridging oxygen (Si-O-Si) peaks are partially resolved in $^{17}O$ MAS NMR spectrum for iron-free silicate glass, it is difficult to distinguish the oxygen clusters in iron-bearing silicate glass. The Lorentzian peak shape for $^{29}Si$ and $^{17}O$ MAS NMR spectra may reflect life-time broadening due to spin-electron interaction. These results demonstrate that solid-state NMR can be an effective probe of the detailed structure in iron-bearing silicate glasses.

• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 2004.07b
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• pp.927-931
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• 2004

본 논문에서는 혈당측정기 제작에 있어 PDMS(Su-8)를 이용하였다. 이는 일종의 고분자로서 기계적 특성이 우수하고 제작이 간단하며, 가격이 저렴하고 다른 물질과의 접합이 용이하다. 혈액의 펌핑과 믹싱을 할 수 있도록 새로운 구조체를 설계하였으며 제안된 모델의 핵심 부분인 측정전극의 제작에 필요한 기초적인 실험을 수행하였다. 측정전극의 성능향상과 제작편의성, 저가격화를 위해 효소고정화방법으로 Electrospinning (전기방사)으로 제조된 PVA nanofiber web을 이용하였으며, 이는 중합도 Pn=1700, 비누화도 98%인 공업용으로 상용화된 값싼 제품이다. 따라서 이를 이용하면 측정용 전극의 효소고정화에 있어 저가격화를 이룰 수 있을 것으로 기대된다 고정화된 전극분석을 위해 SEM(주사전자현미경)과 NMR(핵자기공명분광계), FT-IR(적외선분광분석)장비를 사용하였다. 그리고 기존의 효소고정화법(전기중합법)과의 응답특성을 비교분석하였다.

• Journal of the Mineralogical Society of Korea
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• v.24 no.4
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• pp.289-300
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• 2011

Atomistic origins of carbon solubility into silicates are essential to understand the effect of carbon on the properties of silicates and evolution of the Earth system through igneous and volcanic processes. Here, we investigate the atomic structure and NMR properties of dissolved carbon in enstatite using Raman spectroscopy and quantum chemical calculations. Raman spectrum for enstatite synthesized with 2.4. wt% of amorphous carbon at 1.5 GPa and $1,400^{\circ}C$ shows vibrational modes of enstatite, but does not show any vibrational modes of $CO_2$ or ${CO_3}^{2-}$. The result indicates low solubility of carbon into enstatite at a given pressure and temperature conditions. Because $^{13}C$ NMR chemical shift is sensitive to local atomic structure around carbon and we calculated $^{13}C$ NMR chemical shielding tensors for C substituted enstatite cluster as well as molecular $CO_2$ using quantum chemical calculations to give insights into $^{13}C$ NMR chemical shifts of carbon in enstatite. The result shows that $^{13}C$ NMR chemical shift of $CO_2$ is 125 ppm, consistent with previous studies. Calculated $^{13}C$ NMR chemical shift of C is ~254 ppm. The current calculation will alllow us to assign potential $^{13}C$ NMR spectra for the enstatite dissolved with carbon and thus may be useful in exploring the atomic environment of carbon.

• Journal of the Korean Chemical Society
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• v.57 no.1
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• pp.40-51
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• 2013

In order to develop a quantitation method for Perfluorooctanesulfonic acid(PFOS) contained in plastics that are mainly used in electric and electronic equipment, this study consisted of conducting method validations with LDPE samples using soxhlet solvent extraction and LC/MS. As a result, the limits of detection and quantitation (LOD, LOQ) were $2.58{\mu}g/L$ and $7.82{\mu}g/L$, respectively. Additionally, the recovery was 96-102%. For the correlation coefficient of LC/MS, the $r^2$ value was 0.9992 in the concentration range of $7.82-100{\mu}g/L$, which confirmed its linearity. Furthermore, for the standardization of the analysis method for PFOS in electric and electronic equipment to correspond to EU environmental regulations, we conducted a proficiency test with a number of domestic and international testing laboratories. Three of the ten testing laboratories that participated in the proficiency test submitted outliers. Accordingly, we examined the cause of the outliers using the $^{19}F$ NMR, finding that the main cause was an error in the processing of the results for isomers in PFOS that existed in standard solutions and samples.