• Bulletin of the Korean Chemical Society
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• 제23권5호
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• pp.679-682
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• 2002

Layered Na0.7[Ni0.05Mn0.95]O2 compounds have been synthesized by a sol-gel method, using glycolic acid as a chelating agent. Na0.7[Ni0.05Mn0.95]O2 precursors w ere used to prepare layered lithium manganese oxides by ion exchange for Na by Li, using LiBr in hexanol. Powder X-ray diffraction shows the layered Na0.7[Ni0.05Mn0.95]O2 has an O3 type structure, which exhibits a large reversible capacity of approximately 190 mA h g-1 in the 2.4-4.5 V range. Na0.7[Ni0.05Mn0.95]O2 powders undergo transformation to spinel during cycling.

• 한국연초학회지
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• 제16권2호
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• pp.172-180
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• 1994

This study was carried out to separate and identify the acidic compounds in tobacco leaves. Izmir tobacco leaves was extracted with isopropyl ether and the extract was concentrated. The concentrate was extracted with 6% NaHCO3 aqueous solution. The aqueous extract was acidified with sulfuric acid, and extracted with diethyl ether. The acidic material was fractionated on silicic acid column using a benzene-methanol mixture with a stepwise increasing methanol concentration. The resulting fractions were esterified with diazomethane, and then identified by GC, GC/MS using SPB -5 fused silica capillary column. Most of acidic compounds in Izmir tobacco leaves were elected from fraction B which was benzene-methanol(98 : 2) mixture on silicic acid column chromatography. The identified acidic compounds of Izmir tobacco leaves were 18 saturated acids, 8 unsaturated acids, 5 dicarboxylic acids, 13 aromatic acids and 7 terpenoid acids. The major acidic compounds of lzmir tobacco leaves were 2- methylbutanoic, 3-methyl butanoic, 3- methylpentanoic, hexanoic, nonanedioic, phenylacetic, benzoic, 4- methoxybenzoic, 3, 5- dimethoxybenzoic, methoxycinnamic and 3, 4- dimethoxycinnamic acid. Key Words : Izmir tobacco, Acidic compounds, GC/MS.

• 한국대기환경학회지
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• 제34권1호
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• pp.120-143
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• 2018

The analytical methods and their ambient levels of organic nitrogenous compounds such as nitrosamines, nitramines (nitroamines), imines, amides and nitro-polycyclic aromatic hydrocarbons (nitro-PAHs) in the atmosphere are summarized and discussed. Sampling for the analysis of organic nitrogenous compounds was mostly conducted using high volume air sampler. The direct liquid extraction (DLE) using sonification and the pressurized liquid extraction (PLE) using the accelerated solvent extraction (ASE) have been frequently employed for the extraction of organic nitrogenous compounds in the atmospheric samples. After extraction, clean-up via filtration and the solid phase extraction (SPE) and concentrations using nitrogen and rotary evaporator have been generally conducted but in some studies the clean-up and concentration steps have been omitted to prevent the loss of analyte and improve the recovery rate of the analytical procedure. Instrumental analysis was mainly carried out using gas chromatography (GC) or the high performance liquid chromatography (HPLC) coupled with the single quadrupole mass spectrometer or tandem mass spectrometer in the electron ionization (EI), positive chemical ionization (PCI) and negative chemical ionization (NCI) mode and analysis sensitivity of nitrosamines and nitramines were higher in NCI mode. Desirable sampling and analysis methods for analyzing particulate organic nitrogenous compounds are suggested.

• 한국자원식물학회지
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• 제34권6호
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• pp.566-574
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• 2021

This research was carried out to investigate the correlation between soil chemical properties and bioactive compounds of Acer tegmentosum Maxim. The methods of determining bioactive compounds were determined by high performance liquid chromatography, that contained (-)-gallocatechin (0.04±0.01 ~ 0.43±0.28%), salidroside (0.90±0.06 ~ 3.86±0.59%), tyrosol (0.03±0.00 ~ 0.43±0.00%), (-)-catechin (0.05±0.01 ~ 0.37±0.14%), 6'-O-galloylsalidroside (0.02± 0.01 ~ 0.31±0.06%), (-)-epicatechin-gallate (0.01±0.00 ~ 0.04±0.01%). The soil chemical properties analysis such as soil pH, electric conductivity (EC), organic matter (OM), total nitrogen (TN), available phosphate (Avail. P₂O₅), exchangeable cation and cation exchange capacity (CEC) were performed following the standard manual. The correlation analysis between soil chemical properties and bioactive compounds of A. tegmentosum, soil pH, available phosphate and exchangeable cation (Ca²⁺ and Mg²⁺) were negatively correlated with content of salidroside. On the other hand, soil exchangeable cation (Na⁺) showed positive correlation with content of salidroside. The results of this study was able to investigate the correlation between soil chemical properties and bioactive compounds of A. tegmentosum.

• Bulletin of the Korean Chemical Society
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• 제32권10호
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• pp.3675-3681
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• 2011

Fusarium oxysporum, an important pathogen that mainly causes vascular or fusarium wilt disease which leads to economic loss. Disruption of gene encoding a heterotrimeric G-protein-${\beta}$-subunit (FGB1), led to decreased intracellular cAMP levels, reduced pathogenicity, colony morphology, and germination. The plant defense protein, Nicotiana alata defensin (NaD1) displays potent antifungal activity against a variety of agronomically important filamentous fungi. In this paper, we performed a molecular modeling and docking studies to find vital amino acids which can interact with various antifungal compounds using Discovery Studio v2.5 and GRAMMX, respectively. The docking results from FGB1-NaD1 and FGB1-antifungal complexes, revealed the vital amino acids such as His64, Trp65, Ser194, Leu195, Gln237, Phe238, Val324 and Asn326, and suggested that the anidulafungin is a the good antifungal compound.The predicted interaction can greatly assist in understanding structural insights for studying the pathogen and host-component interactions.

• Archives of Pharmacal Research
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• 제20권3호
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• pp.259-263
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• 1997

In the preparation of acyclic thymidine nucleoside analogues, $K_2CO_3$(or NaH) treated thymine in DMSO was alkylated with .omega.-chloroalkyl nitrite (Cl-(CH_2)n-CN; n=1, 2, 3, 4) to provide an isomeric mixture of 1-(${\omega}$-cyanoalkyl)thymine (2a-d) and 1,3-bis(${\omega}$-cyanoalkyl)thymine in approximately 5:1 ratios. Reduction of the cyano function 2a-d with $NaBH_{4}/CoCl_{2}$ center dot$ 6H_{2}O$gave the corresponding 1-(${\omega}$aminoalkyl)thymine (3a-d). The newly formed primary amino function in 3a-d was directly reacted with 2-chloroethylisocyanate to afford the 1-[.omega.($N^{I}$-2-chloroethylureido) alkyl]thymine (4a-d) in good yields. Nitrosation of 1-[5-($ N^{I}-2$-chloroethylureido)pentyl] thymine (4d) with glacial acetic acid and dry $NaNO_{2}$-powder in anhydrous $CH_{2}Cl_{2}$gave two types of regioisomeric nitrosoureas, 1-[5-($N^{I}$--chloroethyl-$N^{I}$--nitrosoureido)pentylithymine (5d) and 1-[5-($N^{I}-2$-chloroethyl-N-nitrosoureido)pentyllthymine in approximately 5 :1 ratios. The in vitro cytotoxicity of the synthesized compounds (2a-d, 3a-d, 4a-d and 5a-d) against three cell lines (K-562, P-388 and FM-3A) are measured as $IC^{50}$ values. Compounds 3b and 4c showed moderate activities against all three cell lines, and all other compounds were found to be not active.

• 멤브레인
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• 제28권2호
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• pp.96-104
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• 2018

해수담수화의 빠른 증가와 함께 붕소 제거에 대한 중요성이 상승하고 있다. 본 연구는 표면개질 시 친수성 화합물을 이용하여 수투과량을 최대한 막고 붕소 제거율을 높이기 위한 연구를 진행하였다. 첫째로, Control polyamide 역삼투막을 얻기 위해 M-phenylenediamine (MPD)와 trimesoyl chloride (TMC)를 Polysulfone 한외여과막에 계면중합을 시켜 polyamide 활성층을 제조하였다. 다음으로, Control polyamide 역삼투막에 표면개질을 진행시켜 D-gluconic acid (DGCA)와 D-gluconic acid sodium salt (DGCA-Na)를 glutaraldehyde (GA)와 hydrochloric acid (HCl)을 이용하여 합성시켰다. 합성된 역삼투막의 표면 분석을 위해 XPS 분석을 진행하였으며, DGCA 및 DGCA-Na 화합물과의 반응이 되었음을 확인하였다. 또한, morphology 측정을 위해 FE-SEM과 AFM 분석을 진행하였으며, polyamide 활성층 형성 및 표면 거칠기를 확인할 수 있었다. 수투과량의 경우, 표면개질을 진행한 역삼투막은 10 GFD 수준이거나 그 이하의 값을 가졌다. 하지만, DGCA 및 DGCA-Na 화합물과 표면개질을 진행한 역삼투막의 붕소 제거율은 94.38, 94.64%로, Control polyamide 역삼투막보다 각각 12.03, 12.29 %p만큼 큰 값을 가지는 것을 확인할 수 있었다.

• 한국방사성폐기물학회:학술대회논문집
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• 한국방사성폐기물학회 2004년도 학술논문집
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• pp.72-80
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• 2004

국내의 가동 중지된 우라늄 변환시설의 해체 시 다량의 우라늄으로 오염되어 있는 금속성 폐기물의 재활용 또는 자체처분을 위한 제염기술로 중성염 전해액을 사용하는 전해제염 공정의 적용성을 평가하기 위하여 우라늄 변환시설 내부설비의 주 구성 재료인 SUS-304 및 Inconel-600에 대한 전기화학적 용해거동 연구를 수행하였다. 이를 위하여 중성염 전해질의 형태, 전해질의 농도, 전류밀도, 처리시간과 같은 전해제염 조건들이 금속 재료의 용해에 미치는 영향을 평가하였다. 모의 시편을 사용한 비방사성 전해용해 실험 결과를 근거로 실제 우라늄 변환시설로부터 인출한 $UO_2$, AUC (ammonium uranyl carbonate) 및 ADU (ammonium diuranate) 오염시편에 대해 $Na_2SO_4$및 $NaNO_3$ 중성염 용액에서 전해 제염실험을 수행하였으며, 오염물의 종류 및 오염 준위의 대소와는 관계없이 모든 시편에 대하여 10분 이내의 짧은 시간 내에 자체처분 기준치 이하로 $\beta$ 방사능 준위를 감소시킴으로써 본 중성염 전해제염이 매우 성공적임을 확인하였다.

• 한국분말재료학회지
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• 제15권2호
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• pp.125-135
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• 2008

[ $TiO_2$ ] nanotubes for photocatalytic application have been synthesized by hydrothermal method. $TiO_2$ nanotubes are formed by washing process after reaction in alkalic solution. Nanotubes with different morphology have been fabricated by changing NaOH concentration, temperature and time. $TiO_2$ nanoparticles were treated inside NaOH aqueous solution in a Teflon vessel at $110^{\circ}C$ for 20 h, after which they were washed with HCl aqueous solution and deionized water. Nanotube with the most perfect morphology was formed from 0.1 N HCl washing treatment. $TiO_2$ nanotube was also obtained when the precursor was washed with other washing solutions such as $NH_4OH$, NaCl, $K_2SO_4$, and $Na_2SO_3$. Therefore, it was suggested that $Na^+$ ion combined inside the precursor compound slowly comes out from the structure, leaving nanosheet morphology of $TiO_2$ compounds, which in turn become the nanotube in the presence of hydroxyl ion. To stabilize the sheet morphology, the different type of washing treatment solution might be considered such as amine class compounds.

• 한국세라믹학회지
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• 제32권5호
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• pp.582-586
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• 1995

The crystal structures of (Na0.3Sr0.7)(Ti0.7M0.3)O3 (M=Ta, Nb) compounds were determined using the Rietveld method. Due to the tilting of a oxygen octahedron, (Na0.3Sr0.7)(Ti0.7Nb0.3)O3 had a superlattice of doubled a, b and c of simple perovskite. The crystal structure of (Na0.3Sr0.7)(Ti0.7M0.3)O3 was tetragonal with a space group 14/mmm. The crystal structure of (Na0.3Sr0.7)(Ti0.7M0.3)O3 was a cubic with space group Pm3m, in which no tilting of oxygen octahedron was observed. The difference in the oxygen tilting of these two materials was due to the larger covalency of Nb-O bond than that of Ta-O bond, which induced a strong $\pi$Nb0 bonding in (Na0.3Sr0.7)(Ti0.7M0.3)O3. Therefore, the higher transition temperature of (Na0.3Sr0.7)(Ti0.7M0.3)O3 could be related to the larger tilting of oxygen octahedron.