• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 2001.11b
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• pp.7-10
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• 2001

Orthorhombic type $LiCo_{x}Mn_{1-x}O_{2}$(0 ${\times}$ 0.14) oxides have been synthesized by hydrothermal treatment of $(Co_{x}Mn_{1-x})_{3}O_{4}$ precursors and LiOH aqueous solution at $170^{\circ}C$. As-synthesized powders showed well-ordered ${\beta}-NaMnO_{2}$ structures, and the products were single crystalline particle oxides from TEM observations. The particle size decreased with increasing the amount of Co substituent. Much more improved capacity upon 100 cyclings was clearly seen in orthorhombic $LiCo_{0.1}Mn_{0.9}O_{2}$, comparing to orthorhombic $LiMnO_2$.

• Electrical & Electronic Materials
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• v.14 no.12
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• pp.7-10
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• 2001

Orthorhombic type LiCo$_{x}$Mn$_{1-x}$ O$_2$(0$\leq$x$\leq$0.14) oxides have been synthesized by hydrothermal treatment of (Co$_{x}$Mn$_{1-x}$ )$_3$O$_4$precursors and LiOH aqueous solution at 17$0^{\circ}C$. As-synthesized powders showed well-ordered $\beta$-MaMnO$_2$structures, and the products were single crystalline particle oxides from TEM observations. The particle size decreased with increasing the amount of Co substituent. Much more improved capacity upon 100 cyclings was clearly seen in orthorhombic LiCo$_{0.1}$Mn$_{0.9}$O$_2$, comparing to orthorhombic LiMnO$_2$./TEX>.EX>.

• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 2001.11a
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• pp.7-10
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• 2001

Orthorhombic type $LiCo_{x}Mn_{1-x}O_2$ (0 x 0.14) oxides have been synthesized by hydrothermal treatment of ($Co_{x}Mn_{1-x}$)$_3O_4$ precursors and LiOH aqueous solution at $170^{\circ}C$. As-synthesized powders showed well-ordered ${\beta}$-$NaMnO_2$ structures, and the products were single crystalline particle oxides from TEM observations. The particle size decreased with increasing the amount of Co substituent. Much more improved capacity upon 100 cyclings was clearly seen in orthorhombic $LiCo_{0.1}Mn_{0.9}O_2$, comparing to orthorhombic $LiMnO_2$.

• Environmental Engineering Research
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• v.12 no.2
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• pp.72-80
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• 2007

Experiments were conducted to identify the emissions from the car air freshener and to identify the formation of ultra-fine particles and secondary gaseous compounds during the ozone-initiated oxidations with emitted VOCs. The identified primary constituents emitted from the car air freshener in this study were $\alpha$-pinene, $\beta$-pinene, $\rho$-cymene and limonene. Formation of ultra-fine particles (4.4-160 nm) was observed when ozone was injected into the chamber containing emitted monoterpenes from the air freshener. Particle number concentrations, particle mass concentrations, and surface concentrations were measured in time dependent experiments to describe the particle formation and growth within the chamber. The irritating secondary gaseous products formed during the ozone-initiated reactions include formaldehyde, acetaldehyde, acrolein, acetone, and propionaldehyde. Ozone concentration (50 and 100 ppb) and temperature (30 and $40^{\circ}C$) significantly affect the formation of particles and gaseous products during the ozone-initiated reactions. The results obtained in this study provided an insight on the potential exposure of particles and irritating secondary products formed during the ozone-initiated reaction to passengers in confined spaces.

• Particle and aerosol research
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• v.14 no.4
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• pp.107-119
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• 2018

In this study, we have developed a real-time monitoring device for measuring PM10 and PM2.5 of ambient aerosol particles. The real-time PM monitor (SENTRY Dust Monitor) uses the optical scattering method and has 16 channels in particle size. The laboratory and field tests were carried out to evaluate the developed SENTRY Dust Monitor. Arizona Test Dust particles were used as test particles in the laboratory test and the field test was carried out at the Jongno-gu Observatory in Seoul. The measurements of PM10 and PM2.5 concentrations obtained by SENTTRY Dust Monitor were compared with Grimm Dust Monitor (Model 1.108) and a beta ray gauge. It was shown that the PM10 and PM2.5 concentrations obtained by SENTRY Dust Monitor agree well with that of the reference devices. Based on the results obtained in this study, it could be concluded that the SENTRY Dust Monitor can be used as a PM monitoring device for real-time monitoring of the ambient aerosols.

• The Bulletin of The Korean Astronomical Society
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• v.44 no.1
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• pp.49.1-49.1
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• 2019

Giant radio relics in the outskirts of galaxy clusters have been observed and they are interpreted as synchrotron emission from relativistic electrons accelerated via diffusive shock acceleration (DSA) in weak shocks of Ms < 3.0. In the DSA theory, the particle momentum should be greater than a few times the momentum of thermal protons to cross the shock transition and participate in the Fermi acceleration process. In the equilibrium, the momentum of thermal electrons is much smaller than the momentum of thermal protons, so electrons need to be pre-accelerated before they can go through DSA. To investigate such electron injection process, we study the electron pre-acceleration in weak quasi-perpendicular shocks (Ms = 2.0 - 3.0) in an ICM plasma (kT = 8.6 keV, beta = 100) through 2D particle-in-cell simulations. It is known that in quasi-perpendicular shocks, a substantial fraction of electrons could be reflected upstream, gain energy via shock drift acceleration (SDA), and generate oblique waves via the electron firehose instability (EFI), leading the energization of electrons through wave-particle interactions. We find that such kinetic processes are effective only in supercritical shocks above a critical Mach number, $Ms{\ast}{\sim}2.3$. In addition, even in shocks with Ms > 2.3, energized electrons may not reach high energies to be injected to DSA, because the oblique EFI alone fails to generate long-wavelength waves. Our results should have implications for the origin and nature of radio relics.

• Journal of Korean Society for Atmospheric Environment
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• v.33 no.6
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• pp.616-625
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• 2017

Measurements using five real-time particle samplers were compared to measurements using three NRM (National Reference Method system) filter-based samplers(Gravimetric method) at Incheon, Korea, between May and August, 2014. The purpose of this study was to suggest the quality assurance/quality control (QA/QC) method of each instrument for use in a real-time continuous particle sampler to measure the mass of airborne particles with an aerodynamic diameter less than $2.5{\mu}m$ ($PM_{2.5}$). Five real-time particle samplers of BAM1020, FH62C_14, TEOM, PM-711 and SPM-613 were evaluated by comparing its measured 23 hr average $PM_{2.5}$ concentrations with those measured with NRM filter-based samplers simultaneously. The parameters(e.g. Inlet heating condition, Slope factor, Film response, Intercept, Background, Span value) of the real-time samplers were optimized respectively by conducting test performance evaluation during 7 days in field sampling. For example, inlet heating temperature of TEOM sampler controls $35{\sim}40^{\circ}C$ to minimize the fluctuation of the real-time measurement data and background value of BAM1020 is the key factor affecting the accuracy of $PM_{2.5}$ mass concentration. We classified the $PM_{2.5}$ concentration according to relative humidity (80%) to identify water absorbed in aerosols by measuring the ${\beta}$-ray samplers(BAM1020, FH62C_14) and TEOM. ${\beta}$-ray samplers were not strongly affected by relative humidity that the difference of the average $PM_{2.5}$ concentration was about 5%. On the other hand, The TEOM sampler overestimated $PM_{2.5}$ mass concentration about 15% at low relative humidity (<80%).

• Nuclear Engineering and Technology
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• v.49 no.7
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• pp.1483-1488
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• 2017

In order to predict and control the environmental and health impacts of ionizing radiation in environmental sources such as groundwater, it is necessary to identify the radionuclides present. Beta-emitting radionuclides are frequently identified by measuring their characteristic energy spectra. The present work shows that self-attenuation effects from volume sources result in a geometry-dependent shift in the characteristic spectra, which needs to be taken into account in order to correctly identify the radionuclides present. These effects are shown to be compounded due to the subsequent shift in the photon spectra produced by the detector, in this case an inorganic solid scintillator ($CaF_2:Eu$) monitored using a silicon photomultiplier. Using tritiated water as an environmentally relevant, and notoriously difficult to monitor case study, analytical predictions for the shift in the energy spectra as a function of depth of source have been derived. These predictions have been validated using Geant4 simulations and experimental results measured using bespoke instrumentation.

• The Korean Journal of Rheology
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• v.9 no.1
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• pp.40-46
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• 1997

폴리이소부틸렌(PIB)/폴리부텐(PB) 고분자 용액에 분산된 입자의 영향을 살펴보기위 해 제조된 kaolinite/PIB/PB 용액에 대한 Weissenberg 효과와 유변학적 물성을 조사하였다. Kaolinite 분산 PIB/PB 고분자 용액도 2차 유체로 간주될수 있음이 발견되었으며 느린 변형 속도에서 2차유체로 간주되는 입자 분산 고분자 용액에 대한 막대상승 실험에서 얻는 고분 자 용액의 탄성 발현에 의한 상승높이에 비례하는 막대오름상수 $\beta$값으로부터 유변학적 특 서치들을 구할수 있었다. 이러한 막대오름상수 $\beta$값은 PIB/PB 및 kaolinite/PIB/PB계에서 용매 점도, 입자 농도와 PIB의 농도가 높을수록 증가하는 반면 온도에는 반비례함을 보이는 데 고분자 용융체에서와는 달리 입자 분산고분자 용액의 경우 입자의 농도가 증가함에 따라 탄성도 증가하는 특징적 거동을 관찰하였다. 한편 Physica MC-120과 RMS 800 Rheometer 를 사용하여 PIB 고분자 용액의 유변학적 물성들을 측정하였으며 2차 유체 구성방정식에 근거하여 얻어지는 유변학적 특성치들과 비교하였다.

• Journal of the Korean Ceramic Society
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• v.32 no.7
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• pp.832-838
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• 1995

The densifying behavior of ultrafine amorphous Si3N4 (about 20 nm)-$\beta$-SiC (about 40~80 nm) powders (O2 : 1.3~15wt%, 0$700^{\circ}C$ within 15 sec and then immediately cooled and held at 135$0^{\circ}C$ for 10 min in N2 atmosphere without resorting to additives using a Xe image heating apparatus. Using an ultrafine pure Si3N4 powder with particle size less than 30nm, further more, mixed with an appropriate amount of $\beta$-SiC, was found to be advantageous to obtain uniform and homogeneous microstructure. In addition, ultrafine Si3N4 powders were also proved to be effective as sintering additive on densifying large sized Si3N4 powder compacts.