• Bulletin of the Korean Chemical Society
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• v.31 no.4
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• pp.989-998
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• 2010

The titled dye of DBPI gives amplified spontaneous emission (ASE) with maximum at 580 nm upon pumping by nitrogen laser (${\lambda}_{ex}\;=\;337.1\;nm$). The ground state absorption cross section (${\sigma}_A$) and emission cross section (${\sigma}_E$) as well as effective emission cross section(${\sigma}^*_E$) have been determined. The electronic absorption spectra of DBPI were measured in ethanol and tetrahydrofuran at room and low temperature. DBPI displays molecular aggregation in water. The photochemical reactivity of DBPI was also studied in carbon tetrachloride upon irradiation with 525 nm light. The electrochemical investigation of DBPI dye has been carried out using cyclic voltammetry and convolution deconvolution voltammetry combined with digital simulation technique at a platinum electrode in 0.1 mol/L tetrabutyl ammonium perchlorate (TBAP) in two different solvents acetonitrile ($CH_3CN$) and dimethylformamide (DMF). The species were reduced via consumption of two sequential electrons to form radical anion and dianion (EE mechanism). In switching the potential to positive direction, the compound was oxidized by loss of two sequential electrons, which were followed by a fast dimerization and/or aggregation process i.e $EC_{dim1}EC_{dim2}$ mechanism. The electrode reaction pathway and the chemical and electrochemical parameters of the investigated compound were determined using cyclic and convolutive voltammetry. The extracted electrochemical parameters were verified and confirmed via digital simulation method.

• Bulletin of the Korean Chemical Society
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• v.35 no.4
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• pp.989-993
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• 2014

The molecular structures of 2,6-diaza-1,3,5,7-tetraoxaspiro[3,3]heptane (1) and its dinitro derivative, 2,6-dinitro-2,6-diaza-1,3,5,7-tetraoxaspiro[3,3]heptane (2), were fully optimized without symmetry constraints at $HF/6-31G^*$ level of theory. A bisected conformation with respect to the ring is preferred with a $C_2$ symmetric structure. The density of each molecule in the crystalline state was estimated to 1.12 and 2.36 $g/cm^3$ using PM3/VSTO-3G calculations from the molecular volume. The heat of formation was calculated for two compounds at the CBS-4M level of theory. The detonation parameters were computed using the EXPLO5 software: D = 6282 m/s, $P_{C-J}$ = 127 kbar for compound 1, D = 7871 m/s, $P_{C-J}$ = 307 kbar for compound 2, and D = 6975 m/s, $P_{C-J}$ = 170 kbar for 60% compound 2 with 40% TNT. Specific impulse of compound 1 in aluminized formulation when used as monopropellants was very similar to that of the conventional ammonium perchlorate in the same formulation of aluminum.

• Proceedings of the Korean Society of Propulsion Engineers Conference
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• 2010.05a
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• pp.390-393
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• 2010

The thermal decomposition rate of ammonium perchlorate with 3% of yellow iron oxide, FeOOH was found to be much faster than with red iron oxide, $Fe_2O_3$. By applying yellow and red iron oxide as a burning rate modifier to HTPB/AP propellant, burning rate of the HTPB/AP propellant with yellow iron oxide was shown to be 10 ~ 25% faster than with red iron oxide. There was no special difference in viscosity and hardness buildup of yellow and red oxide added HTPB/AP formulations.

• Proceedings of the Korean Society of Propulsion Engineers Conference
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• 2017.05a
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• pp.978-983
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• 2017

Ammonium dinitramide(ADN) is currently under inder investigation as a replacement for ammonium perchlorate, both for environmental and toxicological reasons. Another promising application is ADN-based liquid monopropellant as a replacement for hydarzine, which is highly toxic and carcinogenic. Production of ADN is today normally performed via guanylurea dinitramide(GUDN) by reaction with potassium hydroxide to yiela potassium dinitramide(KDN). In a second reaction step, KDN is reacted with ammonium sulfate to give ADN. In our new improved process, ADN is synthesized from GUDN in one single reaction step. The simplified process improves purity, reduces the amount of by-products and allows production of ADN at a potentially lower cost, which is crucial to favour the use of ADN.

• Proceedings of the Materials Research Society of Korea Conference
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• 2009.05a
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• pp.57.2-57.2
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• 2009

퍼클로레이트 이온($ClO_4^-$)는 자연적으로 혹은 인공적으로 만들어지며 퍼클로릭산이나 암모늄 퍼클로레이트나, 포타슘 퍼클로레이트 혹은 소듐퍼클로레이트 염의 형태로 존재하며, 물에 아주 잘 녹고, 끓여도 제거되지 않으며, 활성 탄소와 같은 광물에도 흡착 되지 않는 성질로 인해, 기존 물리적인 정수 방법으로는 제거하기 어렵다. 또한 우리 몸에 흡수되면, 요오드가 갑상선에 흡수되는 작용을 방해하여 갑상선 기능장애를 초래한다. 이러한 퍼클로레이트 이온의 제거방법으로는 이온교환법이나 생물학적 방법 등이 개발되어져 있으나, 제거 시스템에 이동 및 안전한 농도까지 제거 등의 문제점으로 인한 퍼클로레이트 이온을 환원시키는 촉매 환원 반응에 의한 퍼클로레이트 이온 제거 기술 개발이 필요하다. 이런 촉매 환원에 필요한 수소 환원제를 발생시키기 위해서, 본 연구에서는 Carbon felt 위에 DC magnetron sputtering에 의한 thin film $TiO_2$과 regine을 이용한 powder $TiO_2$ 시편을 제작하였다. 이렇게 제작 된 $TiO_2$/Carbon felt의 미세구조 및 특성은 XRD, SEM, UV-vis-NIR 등을 통하여 분석하였다. UV 조사에 의해 $TiO_2$/Carbon felt 시편의 산소와 수소 발생과 DC bias의 걸어주었을 때 산소와 수소 발생 차이 등을 비교하였고, 이에 따른 퍼클로 레이트 이온의 분해 영향을 알아보았다.

• The Korean Journal of Physiology and Pharmacology
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• v.19 no.1
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• pp.35-42
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• 2015

In cardiovascular disorders, understanding of endothelial cell (EC) function is essential to elucidate the disease mechanism. Although the mouse model has many advantages for in vivo and in vitro research, efficient procedures for the isolation and propagation of primary mouse EC have been problematic. We describe a high yield process for isolation and in vitro culture of primary EC from mouse arteries (aorta, braches of superior mesenteric artery, and cerebral arteries from the circle of Willis). Mouse arteries were carefully dissected without damage under a light microscope, and small pieces of the vessels were transferred on/in a Matrigel matrix enriched with endothelial growth supplement. Primary cells that proliferated in Matrigel were propagated in advanced DMEM with fetal calf serum or platelet-derived serum, EC growth supplement, and heparin. To improve the purity of the cell culture, we applied shearing stress and anti-fibroblast antibody. EC were characterized by a monolayer cobble stone appearance, positive staining with acetylated low density lipoprotein labeled with 1,1'-dioctadecyl-3,3,3',3'-tetramethyl-indocarbocyanine perchlorate, RT-PCR using primers for von-Willebrand factor, and determination of the protein level endothelial nitric oxide synthase. Our simple, efficient method would facilitate in vitro functional investigations of EC from mouse vessels.

• Journal of the Korean Society of Propulsion Engineers
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• v.9 no.2
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• pp.40-45
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• 2005

In the present work, the effect of formulation on friability of HTPB/AP propellants including Betacene and $Cr_2O_3$ has been studied. The mechanical properties and burning rate of the propellants were measured using Inston tensile tester and strand burner, respectively. Friability was calculated from shot-gun and closed bomb test data. The result showed that friability was higher, as the content of Butacene or AP $6{\mu}m$ in the propellant formulations was increased.

• Journal of the Korean Society of Propulsion Engineers
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• v.9 no.2
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• pp.46-53
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• 2005

We have analyzed the temperature and humidity aging test results of a composite solid propellant. The temperature aging test was performed to evaluate the storage life of a propellant, while the humidity aging test could provide the hygroscopicity of Ammonium Perchlorate(AP) exposed to .elative humidity (RH) 10, 30, $50\%$ environment. A specimen was used in the temperature test, and a block of propellant from the actual motor was used in the humidity test. We report that the 4-month storing at 60 degree is equivalent to the 10-year 60 degree condition. The composite solid propellant with HTPB binder showed signs of hardening with time lapse but the effect of humidity up to RH $50\%$ was not noticeable.

• Journal of the Korean Society of Propulsion Engineers
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• v.16 no.4
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• pp.16-22
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• 2012

We performed impact test to estimate necessary explosive charge weight for cutting the cable whose diameter is 22 mm. The impact test results were analyzed by Probit method. The cutting energy was calculated 37.7 J with 99.99% probability at 99% reliability compared to the average energy of 24.9 J. The cable was cut 3 times without failure with 150 mg of Zirconium Potassium Perchlorate (ZPP), which was considered to generate 24.5 J of mechanical energy with assumption that only 10% of explosive energy converts to mechanical energy. The calculated energy from measured pressure with 150 mg ZPP was 26.1 J, which is almost same with both impact test result and expected mechanical energy. We can argue that the cable can be cut with 99.99% probability at 99% reliability by 230 mg of ZPP.

• Bulletin of the Korean Chemical Society
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• v.17 no.2
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• pp.173-179
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• 1996

A series of tetradentate Schiff base ligands; [1,2-bis(naphthylideneimino)ethane, 1,3-bis(naphthylideneimino)propane, 1,4-bis(naphthylideneimino)butane, and 1,5-bis(naphthylideneimino)pentane] and their Ni(Ⅱ) complexes have been synthesized. The properties of these ligands and their Ni(Ⅱ) complexes have been characterized by elemental analysis, IR, NMR, UV-vis spectra, molar conductance, and thermogravimetric analysis. The mole ratio of Schiff base to Ni(Ⅱ) metal was found to be 1:1. The electrochemical redox process of the ligands and their Ni(Ⅱ) complexes in DMF and DMSO solution containing 0.1 M tetraethyl ammonium perchlorate (TEAP) as a supporting electrolyte have been investigated by cyclic voltammetry, chronoamperometry, differential pulse voltammetry, and controlled potential coulometry at glassy carbon electrode. The redox process of the ligands was highly irreversible, whereas redox process of Ni(Ⅱ) complexes were observed as one electron transfer process in quasi-reversible and diffusion-controlled reaction. The electrochemical redox potentials of the Ni(Ⅱ) complexes were affected by the chelate ring size of ligands. The diffusion coefficients of Ni(Ⅱ) complexes containing 0.1 M TEAP in DMSO solution were determined to be 5.7-6.9 × 10-6 cm2/sec. Also the exchange rate constants were determined to be 1.8-9.5 × 10-2 cm2/sec. These values were affected by the chelate ring size of ligands.