• Proceedings of the Korean Vacuum Society Conference
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• 2011.02a
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• pp.414-414
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• 2011

핵융합로는 고온의 고밀도 플라즈마에 노출되므로 고 열부하 및 플라즈마 이온에 의한 물성수치를 충분히 고려한 재질로 구축하여야 한다. 특히 핵융합의 연료인 중수소, 삼중수소와 관련하여 플라즈마 대면 부품, 블랑켓, 열 교환기 등의 구축재질에 대한 수소동위원소의 누설거동 데이터 확보는 삼중수소의 취급 및 안전성과 경제성 측면에서 매우 중요하다. 현재 국내의 삼중수소 누설거동과 관련된 실험장치 개발 및 데이터는 관련 연구가 진행되는 선진국에 비해 초보적인 수준이며, 핵융합 기술의 자력개발을 위해서도 수소동위원소 관련 누설거동 데이터의 확보는 매우 중요하다. 본 연구는 삼중수소 누설거동 해석을 위한 예비 실험으로, 수소를 사용하는 누설거동 실험장치를 설계 제작하여 기초실험을 수행하였다. 시편은 스테인레스 스틸(SS-316L)을 사용하였으며, 시편의 두께를 변화시켜가며 수소에 대한 activation energy, permeability, diffusivity, solubility를 구한 후 타 연구그룹의 실험결과와 비교 하였다.

• Analytical Science and Technology
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• v.35 no.6
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• pp.249-255
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• 2022

In this study, a new method for the analysis of high-purity nitrogen was developed. A gas chromatography-flame ionization detector (GC-FID) was used for purity analysis. Certified reference materials (CRMs) at a level of 3 µmol/mol of carbon monoxide (CO), carbon dioxide (CO₂), and methane (CH₄), which may exist in high-purity nitrogen, were prepared using the gravimetric method, and these CRMs were used for purity analysis. In this new method, ultra-high-purity and high-purity nitrogen were used as carrier gases. The impurities in high-purity nitrogen were quantitatively analyzed by comparing the differences in the area values of the GC chromatograms of the prepared CRMs. We purchased liquid nitrogen and three bottles of nitrogen gas, which were produced by three different manufacturers, using high-purity nitrogen. Furthermore, to validate the developed purity analysis method, the fraction of impurities in high-purity nitrogen was compared with the results of the typical purity analysis method. The comparison results were consistent within the expanded uncertainties (k = 2).

• Korean Chemical Engineering Research
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• v.60 no.3
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• pp.407-413
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• 2022

This study demonstrates a method for synthesis of amine functionalized and easily size controllable silica nanoparticles through biomimetic polyamine complex. First, we generate a polyamine nanocomplex composed of polyallylamine hydrochloride (PAH) and phosphate ion (pi) to synthesize silica nanoparticles. The size of polyamine nanocomplex is reversibly adjusted within the range of about 50 to 300 nm according to the pH conditions. Amine groups of the PAH in the nanocomplex catalyzes the condensation reaction of silicic acid. As a results, silica nanoparticles are synthesized based on nanocomplex in a very short time. Finally, we synthesize silica nanoparticles with various sizes according to the pH conditions. In the process of synthesizing silica nanoparticles, polyamine chains that act as catalysts are incorporated into the inside and surface of the particles, subsequently, amine groups are exposed on the surface of silica nanoparticles. As a results, the synthesis and surface modification of silica nanoparticles are performed simultaneously, and the silica nanoparticles introduced with amine groups can be easily synthesized by adjusting the sizes of the silica nanoparticles. Finally, we demonstrate the synthesis of functional silica nanoparticles in a short time under milder conditions than the conventional synthetic method. Furthermore, this method can be applicable to bioengineering and materials fields.

• Journal of the Korean Electrochemical Society
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• v.2 no.2
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• pp.81-87
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• 1999

Poly-acrylonitrile (PAN) based carbon fibers were stabilized under various tensions in the presence of air at about $200^{\circ}C$ and sequentially carbonized under some different gas environments in the range of 700 to $1500^{\circ}C$. The prepared carbon fibers were used for rechargeable lithium ion battery anode to investigate preparation parameters effects on electrochemical characteristics. It was found that the tension during stabilization, carbonization temperature and gas atmospheres affect the carbon fiber properties such as conductivity, mechanical strength, surface morphology and diffusion coefficient of lithium ion, which are closely related to the on electrolchemical properties as well as the charge/discharge characteristics.

• Journal of the Korean Applied Science and Technology
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• v.31 no.2
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• pp.244-254
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• 2014

The interactions of 4-chlorobenzoic acid with the micellar system of various cationic, nonionic, and mixed surfactant systems were studied by the UV/Vis spectrophotometric method. The solubilization constants ($K_s$) of 4-chlorobenzoic acid into those micellar systems have been measured at various temperatures and various thermodynamic parameters for the solubilization of 4-chlorobenzoic acid have been calculated and analyzed from those changes. The results show that the values of ${\Delta}G^o_s$ are all negative within the measured temperature range and that the values of ${\Delta}H^o_s$ and ${\Delta}S^o_s$ are all positive. The effects of alkyl-group's length of surfactant molecules on the solubilization of 4-chlorobenzoic acid have been also measured. The values of $K_s$ were dependent simultaneously on the alkyl-group's length and the kind of head-group in surfactant molecules. From these changes we can postulate the solubilization site and the degree of interaction of 4-chlorobenzoic acid with the micellar systems.

• Journal of the Korean Society of Marine Environment & Safety
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• v.16 no.4
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• pp.321-337
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• 2010

Long-term trends and distribution patterns of water quality were investigated in the Mokpo coastal areas of the Yellow Sea, Korea from 1979 to 2009. Water samples were collected at 5 stations and physicochemical parameters were analyzed including water temperature, salinity, suspended solids (SS), chemical oxygen demand (COD), dissolved oxygen (DO) and nutrients. Spatial distribution patterns of temperature, pH and DO were not clear among stations but the seasonal variations were distinct except ammonium. The trend analysis by principal component analysis (PCA) during 30 years revealed the significant variations in water quality in the study area. Spatial water qualities were discriminated into 3 clusters by PCA; station cluster 1, 2~4, and 5. Annual water qualities were clearly discriminated into 4 surface water clusters and 2 bottom water clusters by PCA. By this multi-variate analysis, the annual trends were summarized as the followings; water temperature, pH and COD tended to increase from late 1980's, salinity to decrease, phosphate to increase from 1994 and dissolved inorganic nitrogen to increase, due to the input of fresh water same as shown in Kyoungin coastal area, Asan coastal area, Choensoo bay and Gunsan coastal area.

• Journal of the Korean Chemical Society
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• v.55 no.3
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• pp.444-453
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• 2011

VO(II), ZrO(II), Hf(IV), $UO_2$(II), Sn(II), V(V)$O_3$, Ru(III), Cd(II), Ho(III) and Yb(III) complexes of N'-(2-hydroxybenzyl)-2-(phenylamino)acetohydrazide ($H_2L^1$, 1) and N'-((3-hydroxy-naphthalen-2-yl)methylene)-2-(phenylamino)-acetohydrazide ($H_2L^2$, 13) have been synthesized and characterized by elemental analyses, $^1H$ NMR, IR, UV-Vis, conductance, thermal analyses (DTA and TG). The spectral data showed that the ligands behave as neutral bidentate, monobasic bidentate, monobasic tridentate or bibasic tridentate ligand bonded to the metal ions through the azomethine nitrogen atoms, phenolic hydroxyl group in protonated or deprotonated form and enolic or ketonic carbonyl group. The ligands and their metal complexes exhibit higher antifungal and antibacterial inhibitory effects than parent ligands and the solution of metal ions. Most of metal complexes exhibit higher antifungal activity than standard antifungal drug (amphotricene B). It is also clear that the ligands and their metal complexes have higher antifungal activity than antibacterial activity.

• Journal of the Mineralogical Society of Korea
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• v.28 no.1
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• pp.51-60
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• 2015

We applied gemological analytical approaches on Aquamarine from the Gilgit-Baltistan of Northern Areas, Pakistan. The standard gemological testing indicates that they are consistent with general characteristics of natural aquamarines. We have identified the inclusions of Tantalite-Mn by Raman analysis. It indicates that they occurs in association with the veins of Be-rich coarse pegmatite. And the results of chemical analyses, infrared absorption spectroscopy and Raman spectroscopy indicate that $H_2O$ molecules in channel mostly exist in Type-I and a little Type-II with low alkali ion. The comparison of relative peak intensity of FT-IR analysis can be used for prediction of $Na_2O$ content within not only emerald but also aquamarine.

• Journal of the Korean Chemical Society
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• v.33 no.6
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• pp.623-632
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• 1989

The positions and interaction energies of framework atoms and water molecules of $Mn^{2+}$-exchanged zeolite A were calculated using some potential energy functions and an optimization program. The sum of interaction energies of framework atoms in dehydrated $Mn_{4,5}Na_3-A$ was approximately the same as those of thermally stable $Ca^{2+}$-or $Mg^{2+}$-exchanged zeolite A. Since $Mn^{2+}$ ions can form good coordination bonds with framework oxygens even in dehydrated state, $Mn^{2+}$-exchanged zeolite A is considered to be thermally stable. The optimized positions of framework atoms and ions in this work are agreed well with the crystallographic data. Three groups of water molecules are found in hydrated $Mn^{2+}$-exchanged zeolite A; W(I) group of water molecules having only hydrogen bonds, W(II) group coordinated to $Na^+$ ion, and W(III) group coordinated to $Mn^{2+}$ ion. The average binding energy of each group of water molecules decrease in the order of W(III) > W(II) > W(I). The activation energies in the dehydration reaction of each group of water molecules increased in accordance with their binding energy.

• Membrane Journal
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• v.19 no.3
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• pp.228-236
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• 2009

ABA type triblock copolymer of poly(hydroxyl ethyl acrylate )-b-polystyrene-b-poly(hydroxyl ethyl acrylate), i.e. PHEA-b-PS-b-PHEA, was synthesized throughatom transfer radical polymerization (ATRP). This block copolymer was thermally crosslinked with 4,5-imidazole dicarboxylic acid (IDA) via the esterification between the -OH groups of PHEA in block copolymer and the -COOH groups of IDA. Upon doping with ${H_3}{PO_4}$ to form imidazole-${H_3}{PO_4}$ complexes, the proton conductivity of membranes continuously increased with increasing ${H_3}{PO_4}$ content. The PHEA-b-PS-b-PHEA/IDA/${H_3}{PO_4}$ polymer membrane with [HEA]:[IDA]:[${H_3}{PO_4}$]=3:4:4 exhibited a maximum proton conductivity of 0.01 S/cm at $100^{\circ}C$ under anhydrous conditions. Thermal gravimetric analysis (TGA) shows that the PHEA-b-PS-b-PHEA/IDA/${H_3}{PO_4}$ complex membranes were thermally stable up to $350^{\circ}C$, indicating their applicability in fuel cells.