• Bulletin of the Korean Chemical Society
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• 제13권4호
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• pp.363-367
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• 1992

The crystal structure of (1,3,6,9,11,14-hexaazatricycol[12.2.1.$1^{6,9}$]octadecane)copper(Ⅱ) perchlorate, Cu($C_{12}H_{26}N_6$)$(ClO_4)_2$, has been determined by the X-ray diffraction methods. The crystal data are as follows: Mr=516.9, triclinic, ${\alpha}=8.572\;(2)$, b=8.499 (3), c=15.204 (3) ${\AA}$, ${\alpha}=80.42\;(5),\;{\beta}=73.57\;(3),\;{\gamma}=69.82\;(4)^{\circ},\;V=994.2\;{\AA}^3,\;D_C=1.726\;gcm^{-3}$, space group $P{\tilde{1}},\;Z=2,\;{\mu}=21.27\;cm^{-1}&, F(000)=534 and T=297 K. The structure was solved by direct methods and refined by full-matrix least-squares methods to and R value of 0.081 for 1608 observed reflections measured with graphite-mono-chromated Mo Ka radiation on a diffractometer. There are two independent complexes in the unit cell. The two copper ions lie at the special positions (1/2, 0, 0) and (0, 1/2, 1/2)and each complex possesses crystallographic center of symmetry. Each Cu ion is coordinated to four nitrogen donors if the hexaazamacrotricyclic ligand and weakly interacts with two oxygen atoms of the perchlorate ions to form a tetragonally distorted octahedral coordination geometry. The Cu_N (sec), Cu_N(tert) and Cu_O coordination distances are 1.985 (14), 2.055 (14) and 2.757 (13) ${\AA}$ for the complex A and 1.996 (10), 2.040 (11) and 2.660 (13) ${\AA}$ for the complex B, respectively. The macrocycles in the two independent cations assume a similar conformation with the average r.m.s. deviation of 0.073 ${\AA}$. Two 1,3-diazacyclopentane ring moieties of the hexaazamacrotricyclic ligand are placed oppositely and almost perpendicularly to the square coordination plane of the ruffled 14-membered macrocycle. The secondary N atoms are hydrogen-bonded to the perchlorate O atoms with distances of 3.017 (23) and 3.025 (19) ${\AA}$ for the complexes A and B, respectively.

• 한국섬유공학회:학술대회논문집
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• 한국섬유공학회 2003년도 봄 학술발표회 논문집
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• pp.287-288
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• 2003

Polyurethane(PU) materials have been generally used in the automobile, paint, furniture, adhesive, and textile industries. The use of Waterborne PU was motivated form the environmental point of view, i.e. reduction of solvent emissions into the atmosphere(volatile organic compounds, VOC)[1]. Generally speaking, phase change materials (PCM) have the capability of absorbing or releasing thermal energy to reduce or eliminate heat transfer at the temperature range of the particular temperature stabilizing material[2]. (omitted)

• 한국염색가공학회지
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• 제19권1호
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• pp.37-44
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• 2007

In this study, for textile use, the octadecane of phase change materials(PCM) was encapsulated in several micro-diameter shell which prevents leakage of the material during its liquid phase. Microencapsulated PCM(PM) was prepared with the different weight ratio of core material to wall material and by interfacial polymerization methods using polyurea as shell material. Phase stability for O/W emulsion of PCM and PVA aq. (PE) was evaluated by Turbiscan Lab. The capsule formation win identified using FT-IR. Physical properties of microcapsules including diameter, particle distribution, morphology were investigated. Thermal transport properties of suede treated with PM(SPM) were determined by KES-F7 system.

• 대한기계학회논문집
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• 제11권4호
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• pp.629-636
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• 1987

An experiment is carried out to study the surface-tension driven flow characteristics in a cylindrical liquid column heated from above (which is the low gravity floating zone simulated on earth) with varing the aspect ratio and diameter of the liquid column. Hexadecane, octadecane, silicon oil(10cs), FC-40 and water are used as the test liquids. The free surface shape varies sinusoidally for Ma>M $a_{cr}$ and its frequency is found to be the same as that of temperature oscillation. It is verified that the surface temperature profile changes from linear to S-shaped profile for Ma>M $a_{cr}$ . The frequency of temperature oscillation decreases with increasing liquid volume, while its level increases. M $a_{cr}$ decreases with increasing aspect ratio, and also decreases with increasing Prandtl number in the range of 25

• 한국염색가공학회:학술대회논문집
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• 한국염색가공학회 2008년도 제39차 학술발표회
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• pp.151-152
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• 2008

PCM has the ability to change their state, these materials absorb energy during the heating process as a body contact and release energy during a reverse cooling process as phase change take place. Using the thermal energy storage of PCM which has a melting point 15 to $35^{circ}C$ is one of the most effective ideas for utilization in textile finish. In this study, microencapsulated PCM(MCPCM) were synthesized by sol-gel method using the octadecane(or nonadecane) as PCM and the silica as microcapsule materials. To develop smart temperature adaptable textile, coating process was applied to textile substrate using a composition included MCPCM.

• Bulletin of the Korean Chemical Society
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• 제16권11호
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• pp.1019-1023
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• 1995

A light-emitting silicon material was prepared by electrochemical etching of n-Si single crystal wafers in a solution of hydrofluoric acid and ethanol. Visible photoluminescence from the silicon was inhomogeneous and decayed rapidly in the ambient laboratory conditions or with photoirradiation. Substantial improvements in photoluminescence which include little-dependent luminescence peak energy with excitation energy variation and longer-lasting room temperature visible photoluminescence were achieved when the surface of photoluminescent silicon material was derivatized with the surface modifier of octadecylmercaptan. Surface modification of the photoluminescent silicon was evidenced by the measurements of contact angles of static water drops, FT-IR spectra and XPS data, in addition to changed photoluminescence. Similar improvements in photoluminescence were observed with the light-emitting silicon treated with dodecylmercaptan, but not with octadecane. The present results indicate that sulfurs of octadecylmercaptans or dodecylmercaptans appear to coordinate the surface Si atoms of LESi and perturb the surface states to significantly change the luminescent characteristics of LESi.

• 접착 및 계면
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• 제4권1호
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• pp.35-42
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• 2003

Polystyrene nanocapsules containing octadecane as a core material were prepared by miniemulsion polymerization. The morphology and size of the nanocapsules were measured with varying the surfactant concentration, content of initiator, core/shell ratio and content of comonomer. The morphologies of the prepared nanoparticles were examined by a scanning electron microscope, a transmission electron microscope and the core material was confirmed by a differential scanning calorimeter. The particles below 70 nm in diameter were formed at a high surfactant concentration. The size of the nanoparticles was not significantly affected by the initiator content. With increasing the core/shell ratio and polar comonomer content, the particle size and its distribution were increased.

• 약학회지
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• 제28권1호
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• pp.11-16
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• 1984

As main index of petroleum pollution in the marine organisms n-, iso-paraffins were purified with clean-up method and measured by FID-GC. Ten species of fishes from the near seas of Korea were employed for the study. n-Heptadecane was detected in most fishes. n-Hexadecane and n-octadecane of n-paraffins were highly accumulated in four species of fishes(Seriola quinqueradiata, Sardinia melamosticta, Clupanodon punctatus and Stromateoids argentus), also n-tetradecane and n-hexadecane accumulated in Cololadis saira. Remarkable peak pattern of n-paraffins was not observed in other fishes. Pristane of iso-paraffins was detected in four species of fishes (Sardinia melamosticta, Clupanodon punctatus, Stromateoides orgentus and Cololadis saira).

• 공업화학
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• 제4권3호
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• pp.474-481
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• 1993

무극성, 극성 용매 중 무극성, 극성용질의 무한희석 활동도계수를 가스 크로마토그래피에 의하여 $60^{\circ}C$로부터 $100^{\circ}C$ 범위에서 측정하였다. 무극성용매(n-octadecane)와 극성용매(n-hexadecyl alcohol)에 있어서 무극성용질(alkanes, cyclohexane, benzene, toluene과 $CCl_4$)의 $ln{\gamma}{\infty}$는 1/T 따라 비례하여 증가하였으며, 일정온도에서 동족렬의 $ln{\gamma}{\infty}$는 용질의 탄소수 증가에 따라 비례하여 증가하였다. 극성용질(alcohols, esters and ketones)과 약극성용매(di-2-ethyl adiphate and di-2-ethylhexylsebacate)계에서, 용질의 $ln{\gamma}{\infty}$는 1/T 증가에 따라 변화율이 증가하였으며, 또 일정온도에서 동족렬 용질의 $ln{\gamma}{\infty}$는 탄소수 증가에 따라 반비례하여 감소하였다. 극성용질(alcohols, esters and ketones)은 극성이 큰 용매(triphenyl-phosphate and tricresyl phosphate)계에 있어서, $ln{\gamma}{\infty}$는 1/T 증가에 따라 변화율이 증가하였으며, 일정온도에서 동족렬의 $ln{\gamma}{\infty}$는 용질의 탄소수 증가에 따라 비례하여 증가하였다.

• 한국작물학회지
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• 제40권5호
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• pp.587-593
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• 1995

야생더덕과 재배더덕의 재배장소에 따른 생육특성, 품질 및 향기성분을 비교분석한 결과를 요약하면 다음과 같다. 1. 자생지의 기상환경은 재배지에 비해 기온이 4∼8 낮고 지온도 3 낮았으며 조도량은 재배지의 1.7% 정도였다. 2. 자생지 토양의 환경조건은 재배지 토양에 비하여 pH는 낮았으나 유기물함량은 3배 이상 높았다. 3. 야생더덕과 재배더덕의 염색체 수는 2n =16으로 같았고 자방수도 3개로 동일하였으나, 종자수는 재배더덕이 62개, 야생더덕이 132개로 야생더덕 이 2배 정도 많았다. 4. 야생더덕과 재배더덕의 생육은 재배지보다 자생지에서 저조하였으나 야생더덕은 재배지에서도 재배더덕에 비해 현저하게 떨어졌다. 5. 재배장소에 따른 더덕의 방향성분의 extract수율은 야생더덕은 재배지보다 자생지에서 높았으나 재배더덕은 재배장소에 따른 변화의 차이를 보이지 않았고 extract수율도 50% 정도 낮았다. 6. 재배지에 따른 주요 무기성분함량은 자생지보다 재배지에서 많았으며 야생더덕보다 재배더덕에서 많았다 7. 더덕의 재배장소에 따른 주요 방향성분의 변화는 dimethylbenzene, 3-ethyl-5-2- ( ethylbutyl ) -octadecane, benzaldehyde, 14, 14-dimethyl -hexadecanoate, methylhexadecenoate등이 재배더덕에서는 없는 향기성분이 야생더덕에서 검출되었으며 더덕의 향을 내는 성분은 단일성분이 작용하기 보다는 peak면적이 높게 나타난 성분들이 복합적으로 작용하여 향기를 내는 것으로 판단되었다.