• 한국광물학회지
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• 제21권2호
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• pp.129-138
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• 2008

볼 밀과 임팩트 밀의 분쇄율에 따른 단체분리(선택적 분쇄)와 공기 분급에 의한 고령토 광물의 성세특성을 조사하였다. 원광석을 볼 밀과 임팩트 밀로 분쇄하여 325 mesh 이하 미립자의 생성율을 유사하게 조절하였으며 미립자에 대한 화학성분을 분석함으로써 선택적 분쇄 특성을 조사하였다. 분쇄된 시료는 공기 분급기를 사용하여 미립자와 굵은 입자로 분리하고 각 산물에 대한 화학조성분석을 통하여 분쇄 방식에 따른 정제효과를 비교하였다. 볼 밀과 임팩트 밀 모두 분쇄율이 높아질수록 미립자의 고령토 품위는 낮아지는 경향을 나타내었다. 특히 볼 밀의 경우에서 석영, 장석과 같은 불순광물의 혼입으로 인해 미립자의 불순물 함량이 높아짐을 알 수 있었다. 볼 밀의 경우 공기 분급기의 분급점을 $43\;{\mu}m$로 하면 정광의 생산율은 66.2 wt%이었으며 철성분 제거율은 5.3%, 칼슘성분 제거율은 34.6%로 나타났다. 반면 임팩트 밀을 사용하여 동일한 조건으로 분쇄 후 분급한 산물의 정광 생산율은 64.4 wt%이며 철성분 제거율은 34.2%, 칼슘성분 제거율은 67.6%, 티탄성분 제거율은 25.0%를 나타내어 임팩트 밀의 경우가 불순물의 제거에 우수한 결과를 보였다.

• 한국지반공학회논문집
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• 제32권12호
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• pp.59-67
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• 2016

동결토의 강도는 흙 입자의 크기와 모양, 그리고 얼음과 부동 수분의 양과 같은 요인에 영향을 받는다. 본 연구에서는 동결토의 포화도와 실트 함량에 따라 변화하는 부동 수분의 양과 강도를 평가하고자 하였다. 시료는 주문진사, 실트, 그리고 증류수를 혼합하여 사용하였다. 실트의 함량비(SF)는 주문진사의 중량($W_{sand}$)에 대한 실트 중량($W_{silt}$)의 비율이 10%와 30%가 되도록 혼합하고, 포화도는 5%, 10%, 15%, 그리고 20%가 되도록 조성하였다. 시료는 $-10^{\circ}C$의 챔버 내에서 동결하였고, 동결 시간을 선정하기 위하여 24 시간, 48 시간, 그리고 72 시간동안 동결한 시료에 대하여 일축압축실험을 수행하였다. 일축압축강도가 동결 시간 24 시간 이후에 유사하여 동결 시간은 24 시간으로 선정하였다. 또한, 동결 과정 중 부동 수분의 양을 파악하기 위해 TDR 시스템을 이용하여 시료의 함수비를 모니터링 하였으며, 실트의 함량과 포화도가 증가함에 따라 부동 수분의 양이 증가하였다. 동결이 완료된 시료에 대하여 일축압축실험을 수행하였고, 포화도의 증가에 따라 일축압축강도가 지수함수적으로 증가하는 것으로 나타났다. 포화도가 증가함에 따라 부동 수분의 양이 증가하였으나, 동결에 사용된 물 즉, 얼음이 강도 발현에 보다 큰 영향을 미친 것으로 판단된다.

• 한국재료학회:학술대회논문집
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• 한국재료학회 2012년도 춘계학술발표대회
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• pp.68.1-68.1
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• 2012

The best part of graphene is - charge-carriers in it are mass less particles which move in near relativistic speeds. Comparing to other materials, electrons in graphene travel much faster - at speeds of $10^8cm/s$. A graphene sheet is pure enough to ensure that electrons can travel a fair distance before colliding. Electronic devices few nanometers long that would be able to transmit charge at breath taking speeds for a fraction of power compared to present day CMOS transistors. Many researches try to check a possibility to make it a perfect replacement for silicon based devices. Graphene has shown high potential to be used as interconnects in the field of high frequency electrical devices. With all those advantages of graphene, we demonstrate characteristics of electrical and optical properties of graphene such as the effect of graphene geometry on the microwave properties using the measurements of S-parameter in range of 500 MHz - 40 GHz at room temperature condition. We confirm that impedance and resistance decrease with increasing the number of graphene layer and w/L ratio. This result shows proper geometry of graphene to be used as high frequency interconnects. This study also presents the optical properties of graphene oxide (GO), which were deposited in different substrate, or influenced by oxygen plasma, were confirmed using different characterization techniques. 4-6 layers of the polycrystalline GO layers, which were confirmed by High resolution transmission electron microscopy (HRTEM) and electron diffraction analysis, were shown short range order of crystallization by the substrate as well as interlayer effect with an increase in interplanar spacing, which can be attributed to the presence of oxygen functional groups on its layers. X-ray photoelectron Spectroscopy (XPS) and Raman spectroscopy confirms the presence of the $sp^2$ and $sp^3$ hybridization due to the disordered crystal structures of the carbon atoms results from oxidation, and Fourier Transform Infrared spectroscopy (FTIR) and XPS analysis shows the changes in oxygen functional groups with nature of substrate. Moreover, the photoluminescent (PL) peak emission wavelength varies with substrate and the broad energy level distribution produces excitation dependent PL emission in a broad wavelength ranging from 400 to 650 nm. The structural and optical properties of oxygen plasma treated GO films for possible optoelectronic applications were also investigated using various characterization techniques. HRTEM and electron diffraction analysis confirmed that the oxygen plasma treatment results short range order crystallization in GO films with an increase in interplanar spacing, which can be attributed to the presence of oxygen functional groups. In addition, Electron energy loss spectroscopy (EELS) and Raman spectroscopy confirms the presence of the $sp^2$ and $sp^3$ hybridization due to the disordered crystal structures of the carbon atoms results from oxidation and XPS analysis shows that epoxy pairs convert to more stable C=O and O-C=O groups with oxygen plasma treatment. The broad energy level distribution resulting from the broad size distribution of the $sp^2$ clusters produces excitation dependent PL emission in a broad wavelength range from 400 to 650 nm. Our results suggest that substrate influenced, or oxygen treatment GO has higher potential for future optoelectronic devices by its various optical properties and visible PL emission.

• 한국재료학회지
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• 제4권8호
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• pp.847-854
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• 1994

Mg-Zn-Ce계 합금에서 비정질 단상 및 hcp-Mg입자분산형 비정질합금이 20-40%, Zn, 0-10%Ce과 5-20%Zn, 0-5%Ce 의 조성범위에서 각각 생성되었다. 초미세 hcp-Mg입자분산형 $Mg_{85}Zn_{12}Ce_{3}$비정질합금은 급속응고 또는 급속응고리본의 열처리에 의해 Mg입자의 입경을 4-20nm의 범위로 조절할 수 있었으며, 이 범위에서는 밀착굽힘이 가능할 만큼 충분한 인성을 가지고 있었다. 이 합금의 최대인장강도($\sigma_{B}$)와 파단 연신율($\varepsilon_{f}$)은 hcp-Mg입자의 체적분율에 따라서 670-930MPa, 5.2-2.0%의 범위였으며, 최대 비강도($\sigma_{B}$밀도 =$\sigma_{s}$)는 $3.6 \times 10^5N \cdot m/kg$에 달하였다. 이와 같이 Mg입자분산형 비정질 합금의($\sigma_{B}$), ($\sigma_{s}$)그리고 $\varepsilon_{f}$의 최대치가 Mg-Zn-Ce계 비정질합금(690MPa, $2.5 \times 10^5N \cdot m/kg$, 2.5%)보다 월등하게 높다는 것은 주목할 만 하다. 복합상 조직이 형성됨으로서 기계적 강도가 증가하는 것은 동일 조성의 비정질상보다 강한 hcp과포화 고용체의 분산강화에 기인하는 것이라고 고찰되었다.

• Asian-Australasian Journal of Animal Sciences
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• 제29권4호
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• pp.599-605
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• 2016

In this study, two experiments were conducted to investigate the physicochemical characteristics (Exp. I) of bedding materials such as rice hulls (RH), sawdust (SD), wood shavings (WS) and sawdust+wood shavings (S+W; 1:1 in volume), and utilization of these beddings except RH (Exp. II) for rearing beef cattle. In Exp. I, the distribution of particle size (%) with $250{\mu}m$ and below $250{\mu}m$ was greater (p<0.05) in SD (30.4) than RH (4.4), WS (18.8) and S+W (20.1). Bulk density ($kg/m^3$) of bedding materials was directly proportional to the percentage of $250{\mu}m$ and below $250{\mu}m$ particles, 178, 46, 112, and 88 for SD, WD, S+W and RH, respectively. Water absorption rate (%) after submersion in water for 24 h was higher (p<0.05) in WS (540.2) compared to SD (270.2), S+W (368.2). The S+W had an intermediate value of the absorption rate between SD and WS, but had an outstanding durability of water absorption capacity. Moisture evaporation rate (%) for 12 h was higher (p<0.05) in WS (75.4) than SD (70.5), S+W (72.2) and RH (57.8). Average ammonia emission ($mg/m^2/h$) for 36 h was higher (p<0.05) in RH (3.15) than SD (1.70), WS (1.63), and S+W (1.73). In Exp. II, thirty six Hanwoo cows were allocated in 9 pens with one side on feed bunk side (Side A) and another side equipped with water supply (Side B) for 3 weeks with duplicated periods. Average moisture concentrations (%) of beddings were higher (p<0.05) in WS (side A, 65.7; side B, 57.9) than SD (side A, 62.5; side B, 52.2) and S+W (side A, 61.6; side B, 50.7). Regardless of types of beddings, moisture concentrations (%) of beddings within a pen were lower (p<0.05) at side B than A, implying longer period of utilization. These results suggest that using S+W would be a better choice than SD or WS alone, considering physicochemical characteristics and economics, and RH is not a suitable material as a bedding for beef cattle.

• Journal of Periodontal and Implant Science
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• 제32권4호
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• pp.753-767
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• 2002

The purpose of this study was to evaluate histologically the effect of LiF-maleic acid added calcium aluminate(LM-CA) bone cement & CA-PMMA composite bone cement on the healing of calvarial defect in Sprague-Dawley rats. The critical size defects were surgically produced in the calvarial bone using the 8mm trephine bur. The rats were divided in three groups : In the control group, nothing was applied into the defect of each rat. LM-CA bone cement was implanted in the experimental group 1 and CA-PMMA composite bone cement was implanted in the experimental group 2. Rats were sacrificed at 2, 8 weeks after surgical procedure. The specimens were examined by histologic analysis, especially about the bone-cement interface and the response of surrounding tissue. The results are as follows; 1. In the control group, inflammatory infiltration was observed at 2 weeks. At 8 weeks, periosteum and duramater were continuously joined together in the defect area. But the center of defect area was filled up with the loose connective tissue. 2. In the experimental group 1, the bonding between implanted bone cement and the existing bone was seen, which more increased in 8 weeks than 2 weeks. Inflammatory infiltration and the dispersion of implanted bone cement particles were seen in both 2 weeks and 8 weeks. 3. In the experimental group 2, implanted bone itself had a dimensional stability and no bonding between implanted bone cement and the existing bone was seen in both 2 weeks and 8 weeks. Implanted bone cement was encapsulated by fibrous connective tissue. In addition, inflammatory infiltration was seen around implanted bone cement. On the basis of these results, when LM-CA bone cement or CA-PMMA composite bone cement was implanted in rat calvarial defect, LM-CA bone cement can be used as a bioactive bone graft material due to ability of bonding to the existing bone and CA-PMMA can be used as a graft material for augmentation of bone-volume due to dimensional stability.

• 한국산림과학회지
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• 제100권1호
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• pp.14-24
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• 2011

고로쇠 수피 수용성 추출물의 나노입자화를 통하여 항암활성 증진에 대하여 연구하였다. 먼저 세포독성 측정결과 인간 정상 폐 세포(HEL299)에 대하여 일반 열수 추출물이 1.0 mg/mL의 농도에서 23.51%로 나노입자에 비하여 낮은 세포독성을 나타내었다. 그리고 DPPH radical 소거 활성 실험결과 고로쇠 추출물 나노입자가 높은 항산화 활성을 나타내었고, SOD 유사활성 결과에서도 1.0 mg/mL의 농도에서 32.33%로 일반 열수 추출물에 비하여 높은 항산화 활성을 나타내었다. 인간 위암세포, 간암세포, 유방암세포 그리고 폐암세포에 대하여 암세포 억제 활성 측정결과 고로쇠 추출물 나노입자의 경우 1.0 mg/mL의 농도에서 59-73%의 억제 활성을 나타내었다. 나노입자의 경우 일반 열수 추출물에 비하여 약 5-10% 이상 증진된 활성을 보였다. 그리고 여러 인간 암세포주에 대한 항암실험 결과, 소화기계통의 암세포주에 대하여 71-73%의 암세포 억제 활성을 나타내어 다른 암세포주에 비하여 높은 암세포억제 활성을 보였다. 이러한 결과를 인간 위암세포인 AGS로의 나노입자 침투를 confocal microscope 관찰을 통하여 확인하였다. 위와 같은 결과를 바탕으로 하여 고로쇠 추출물을 나노입자화 공정을 통하여 활성 증진을 확인하였고, 천연 항산화제, 항암소재로서의 활용이 가능할 것으로 사료된다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2014년도 제46회 동계 정기학술대회 초록집
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• pp.409-409
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• 2014

Recently hexagonal boron nitride (h-BN), III-V compound of boron and nitrogen with strong covalent $sp^2$ bond, is a 2 dimensional insulating material with a large direct band gap up to 6 eV. Its outstanding properties such as strong mechanical strength, high thermal conductivity, and chemical stability have been reported to be similar or superior to graphene. Because of these excellent properties, h-BN can potentially be used for variety of applications such as dielectric layer, deep UV optoelectronic device, and protective transparent substrate. Ultra flat and charge impurity-free surface of h-BN is also an ideal substrate to maintain electrical properties of 2 dimensional materials such as graphene. To synthesize a single or a few layered h-BN, chemical vapor deposition method (CVD) has been widely used by using an ammonia borane as a precursor. Ammonia borane decomposes into hydrogen (gas), monomeric aminoborane (solid), and borazine (gas) that is used for growing h-BN layer. However, very active monomeric aminoborane forms polymeric aminoborane nanoparticles that are white non-crystalline BN nanoparticles of 50~100 nm in diameter. The presence of these BN nanoparticles following the synthesis has been hampering the implementation of h-BN to various applications. Therefore, it is quite important to grow a clean and high quality h-BN layer free of BN particles without having to introduce complicated process steps. We have demonstrated a synthesis of a high quality h-BN monolayer free of BN nanoparticles in wafer-scale size of $7{\times}7cm^2$ by using CVD method incorporating a simple filter system. The measured results have shown that the filter can effectively remove BN nanoparticles by restricting them from reaching to Cu substrate. Layer thickness of about 0.48 nm measured by AFM, a Raman shift of $1,371{\sim}1,372cm^{-1}$ measured by micro Raman spectroscopy along with optical band gap of 6.06 eV estimated from UV-Vis Spectrophotometer confirm the formation of monolayer h-BN. Quantitative XPS analysis for the ratio of boron and nitrogen and CS-corrected HRTEM image of atomic resolution hexagonal lattices indicate a high quality stoichiometric h-BN. The method presented here provides a promising technique for the synthesis of high quality monolayer h-BN free of BN nanoparticles.

• 청정기술
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• 제23권1호
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• pp.73-79
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• 2017

기후 변화 대응을 위한 온실가스 감축 측면에서, 석탄화력발전소에서 바이오매스 사용량은 계속하여 증가되어 왔다. 파리 협정 이후 온실가스 감축 목표치가 더욱 구체화되면서 바이오매스 사용은 급격히 더 많아질 것으로 예상된다. 미분탄 석탄 화력발전에서 바이오매스 혼소시 가장 큰 문제점 중 하나는 바이오매스의 미분성이 석탄에 비해 훨씬 낮다는 것으로, 이를 해결하기 위해 가장 먼저 바이오매스의 미분성 측정 방법을 확립하는 작업이 필요하다. 석탄의 경우 HGI (hardgrove grindability index)측정 장치를 통해 분쇄도 측정이 가능하여 이를 표준으로 삼고 있지만, 바이오매스의 경우 표준 측정 방법이 확립되어있지 않다. 본 연구에서는 볼 밀과 입자 크기별 분포량을 이용한 석탄과 바이오매스의 분쇄 실험을 진행하였다. 실험에는 석탄 1종과 바이오매스 6종을 사용하였다. 분쇄시간에 따른 입자 분포량을 비교하고, $75{\mu}m$ 이하 입자 분포량으로 분쇄도를 평가하였다. 실험결과 반탄화 바이오매스 TBC (torrefied biomass chip)와 TWP (torrefied wood chip)는 발전용 사용적합 기준에 대해 대략적으로 70%의 값을 나타냈다. 다른 바이오매스들의 경우 반탄화 바이오매스와 비교했을 때 분쇄성이 훨씬 더 낮은 결과를 보였다. TBC와 TWP는 수분이 감소하고 섬유질 구조가 분해되는 반탄화 과정을 통해 분쇄가 향상되었다. 또한 분쇄도가 높은 반탄화 바이오매스가 소모전력이 낮게 측정되었다. 본 연구를 통해 바이오매스의 석탄화력발전 적용을 위한 표준화 작업의 기초 자료들을 확보할 수 있다.

• 한국재료학회지
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• 제30권11호
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• pp.601-608
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• 2020

In this work, Ag₃PO₄/In₂S₃ nanocomposites with low loading of In₂S₃ (5-15 wt %) are fabricated by two step chemical precipitation approach. The microstructure, composition and improved photoelectrochemical properties of the as-prepared composites are studied by X-ray diffraction pattern (XRD), field emission scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), photocurrent density, EIS and amperometric i-t curve analysis. It is found that most of In₂S₃ nanoparticles are deposited on the surfaces of Ag₃PO₄. The as-prepared Ag₃PO₄/In₂S₃ composite (10 wt%) is selected and investigated by SEM and TEM, which exhibits special morphology consisting of lager size substrate (Ag₃PO₄), particles and some nanosheets (In₂S₃). The introduction of In₂S₃ is effective at improving the charge separation and transfer efficiency of Ag₃PO₄/In₂S₃, resulting in an enhancement of photoelectric behavior. The origin of the enhanced photoelectrochemical activity of the In₂S₃-modified Ag₃PO₄ may be due to the improved charge separation, photocurrent stability and oriented electrons transport pathways in environment and energy applications.