• 한국환경농학회지
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• 제27권4호
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• pp.368-372
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• 2008

돈분 퇴비화 시 Alum 처리 수준이 증가함에 따라 전 퇴비화 과정에서 pH는 낮은 수준으로 유지되었지만, Alum-H 처리구는 퇴비화 초기 pH가 Alum-L와 대조구에 비해 현저히 낮았기 때문에 퇴비화 기간이 지연되었다. 퇴비화 35일 동안 누적 암모니아 휘산량은 Alum-L와 Alum-H 처리구에서 대조구에 비해 각각 31, 78% 감소되었다. Alum 처리는 돈분 퇴비 중 인산을 난용성 인산으로 전환시켜 수용성 인산의 함량을 현저히 감소 시켰다. 따라서 돈분의 퇴비화에 있어 Alum 첨가는 퇴비화 과정에서 질소 손실을 감소시키고, 농경지 활용시 인산 유출량을 저감 할 수 있을 것으로 기대된다.

• Applied Microscopy
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• 제41권2호
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• pp.139-145
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• 2011

담쟁이덩굴(Parthenocissus tricuspidata)은 줄기에 형성된 흡착근으로 접촉 물체표면에 부착하여 식물체를 여러 방향으로 자라게 한다. 이들 흡착근은 접촉면에 일단 착생하면 잘 떨어지지 않는 부착 특성을 지닌다. 본 연구에서는 적벽돌 벽면에 담쟁이덩굴 부착 시 수반되는 흡착근과 벽면 간의 구조적 변화와 함유하는 성분 간의 연관성에 초점을 두어 주사전자현미경과 에너지 분산 X-선 분광분석법으로 비교 연구하였다. 담쟁이덩굴의 흡착근은 적벽돌 표면에 강력 착생하여 벽면을 피복하며 거의 모든 방향으로 생장한다. 이들이 벽 표면에 접촉하는 경우, 흡착근 배축면 내부조직에서 분비하는 점액성 물질에 의해 흡착근-접촉면 간에 상호작용이 일어난다. 접촉면 상에 있는 거친 표면이나 간극 또는 미세한 틈 사이로 침적된 분비물질들에 의해 흡착근과 접촉면은 빈틈없이 밀착된다. 강력 착생한 흡착근조직 내 세포들은 이미 사멸되고, 접촉면에 분비된 물질과 뒤엉키며 수축되어 벽면에서 잘 분리되지 않는 강력한 착생구조체로 변형된다. 접촉면에 착생하였던 흡착근을 분리하여 하피 표면부위에 함유된 원소를 분석한 결과, 이들 흡착근조직의 표면부위에서 적벽돌을 구성하는 주요 성분들이 거의 검출되었다. 이는 착생 전 후 흡착근- 접촉면 사이에서 진행된 물리적인 밀착 및 부착이 구조적 변형과 성분간의 상호작용을 초래하는 것으로 밝혀졌다.

• Restorative Dentistry and Endodontics
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• 제8권1호
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• pp.89-96
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• 1982

The purpose of this study is to identify the phases of four different types, low-copper lathe cut (Type II, class 1) and spherical (Type II, class 2) amalgam alloys which are made by Caulk company and high copper Dispersalloy (Type II, class 3) made by Johnson & Johnson and Tytin (Type I, class 2) made by S.S. White and to determine the Vickers hardness number on the individual phase and four different types of dental amalgam. After each amalgam alloy and Hg measured exactly by the balance was triturated by the mechanical amalgamator (De Trey), the triturated mass was inserted into the cylindrical metal mold which was 4 mm in diameter and 12mm in height and was pressed by the Instron Universal Testing machine (Model 1125) at the speed of 1mm/minute with 143$kg/cm^2$ according to the A.D.A. Specification No. 1. The Specimen removed from the mold, mounted and stored in the room temperature for 7 days. The speciman was polished with the emery paper from #220 to #1200 and finally on the polishing cloth with 0.3 and 0.05 um $Al_2O_3$ powder suspended in water. And then each specimen was etched by Allan's method and washed with Sodium Bisulfinite for 30 seconds. Finally differentiation and metallography on each phase were obtained by using metallographical microscope (Versamet, Union) and microhardness was obtained by using microhardness tester (MVH-2, Torsee). The results were as follows: 1. In the low-copper amalgam, the ${\gamma}$, ${\gamma}_1$ and ${\gamma}_2$ phase were observed and in the high-copper amalgam, the ${\gamma}$, ${\gamma}_1$. ${\epsilon}$ and ${\eta}$ phases were observed but ${\gamma}_2$ phase was not observed. 2. Among the microhardness of each amalgam phase measured under pressing a vickers diamond indenter with 2.0gm load for 30 seconds, e phase has the highest V.H.N (314 ${\pm}$ 20), and in low-copper amalgam 12 phase has the lowest V.H.N. (29${\pm}$1) and ${\eta}$ phase which was observed in high-copper amalgam has 230${\pm}$13 V.H.N and this phase is considerd to contribute to strengthen the handness in amalgam. 3. The V.H.N. measured under pressing a Vickers diamond indenter with 300.0gm load for 30 seconds in low-copper amalgam was lower than that of high-copper amalgam.

• 구강회복응용과학지
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• 제30권2호
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• pp.131-137
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• 2014

목적: 이 연구는 다양한 거칠기를 가진 알루미늄 옥사이드 연마석으로 치주기구 날 세우기를 시행시 연마석의 거칠기에 따른 치주기구 날 세우기의 효율성 및 마모도를 비교 평가하였다. 연구 재료 및 방법: 30개의 No. 9 - 10 그레이시 큐렛이 사용되었고, 모든 큐렛은 치석제거술 및 치근활택술을 시행함으로써 날을 무디게 만들고 3가지 그룹(240, 600, 800 grit)으로 임의로 나누었다. 치주기구의 예민도는 연마석을 최대 20회 기구에 적용한 후 평가되었고, 마모도는 최대 80회 후 기구 날의 끝 1 mm와 2 mm에서 기구 날의 폭으로 평가되었다. 결과: 치주기구 예민도는 5회와 10회 상하 운동시 240 grit에서 유의하게 높게 나타났으며(P < 0.001), 15회, 20회에서는 유의한 차이는 없었다(P > 0.05). 마모도는 240 grit의 경우 600 grit과 800 grit에 비해 약간 높게 나타났지만 통계적 유의성은 없었다. 결론: 알루미늄 옥사이드 연마석의 입자가 클수록 치주기구 날 세우기의 효율성은 증가하였다. 하지만 기구의 마모에 유의해야 한다.

• 한국환경과학회지
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• 제22권7호
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• pp.787-799
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• 2013

The aim of this study was to investigate the accumulation of metallic elements and the control effect of marine pollution caused by ocean dumping in the sediments at a waste disposal area in the Yellow Sea. In July 2009, concentrations of organic matter and metallic elements (Al, Fe, As, Cd, Cr, Co, Hg, Ni, Mn, Pb, and Zn) were measured in surface sediments at the site. The ignition loss (IL) in the surface sediments showed a mean value of 15.4%, about 1.5 times higher than the mean value of the sediments in the coastal areas of Korea. The chemical oxygen demand (COD) at some disposal sites exceeded 20 mg $O_2/g{\cdot}dry$, which signifies the initial concentration of marine sediment pollutants in Japan. The disposal sites contain higher concentrations of Cr, Cu and Zn than the sediments of bays and estuaries that might be contaminated. The magnitude of both metal enrichment factors (EF) and adverse biological effects suggest that pollution with Cr and Ni occurred due to the dumping of waste in the study area. In addition, the geoaccumulation index (Igeo) showed that the surface sediments were moderately contaminated. By the mid-2000s, when the amount of waste dumped at this site was the highest, the concentration of metallic elements was higher than ever recorded. On the other hand, in 2008-09, the need for environmental management was relatively low compare with the peak. As a result, the quality of marine sediment has been enhanced, considering the effect of waste reduction and natural dilution in the disposal area.

• 대한치과보철학회지
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• 제39권1호
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• pp.58-70
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• 2001

For the successful treatment of complete denture, obtaining a good retention is essential. There are lots of factors affecting denture retention. Denture material, one of those factors affecting denture retention, was the subject of this study, and internal surface treatment also considered for the method of enhancing denture retention. Two resin(Lucitone $199^{(R)}$(heat cured resin) Vertex $CP^{(R)}$(self cured resin)) and two metal($Biosil^{(R)}$(Co-Cr alloy), $Vitallium^{(R)}$(Co-Cr alloy)) denture base materials were used for making test denture base. Newly developed device was used for measuring denture retention. After the retention was measured. We treated internal surface of test denture base with $50{\mu}m\;Al_2O_3$ powder, under 90psi, for 1 minute. Then the retention was measured again. The result was analyzed with K-S test, one-way ANOVA test and independent t-test to deter mine the significant differences as the 95% level of confidence. The results are as follows : In cases of without internal surface treatment, the retention was increased in order of $Vitallium^{(R)},\;Biosil^{(R)},\;Vertex CP^{(R)}$ and Lucitone $199^{(R)}$. Except between Vertex $CP^{(R)}$ and $Biosil^{(R)}$, retention of the other materials was significantly different (p<0.05). After the treatment of internal surface, the retention was increased in order of $Vitallium^{(R)},\;Biosil^{(R)},\;Lucno\;199^{(R)},\;Vertex\;CP^{(R)}$. Except between Lucitone $199^{(R)}$ and Vertex $CP^{(R)}$, $Vitallium^{(R)}$ and $Biosil^{(R)}$ the retention of remaining groups was significantly different each other (p<0.05). In the matter of each material, after the internal surface treatment the retention was increased with Vertex $CP^{(R)},\;Biosil^{(R)}\;and\;Vitallium^{(R)}$ and the value of differences were statistically significant. When we compare the retention of resin and metal denture base, the retention of both denture bases increased significantly with internal surface treatment, and resin denture base showed better retention. As the results show, selecting denture base material could be an important choice of complete denture treatment. To increase denture retention, internal surface treatment can be considered as a possible method.

• 한국전기전자재료학회논문지
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• 제26권8호
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• pp.597-601
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• 2013

The accelerated thermal aging of a CSPE were carried out for 0, 80.82, 161.63 days at $100^{\circ}C$, which are equal to 0, 40 and 80 years of aging at $50^{\circ}C$, respectively. The volume electrical resistivities of the seawater and freshwater flooding were measured through 3-terminal circuit diagram. The volume electrical resistivities of the 0y, 40y and 80y were $2.454{\times}10^{13}{\sim}1.377{\times}10^{14}{\Omega}{\cdot}cm$, $1.121{\times}10^{13}{\sim}7.529{\times}10^{13}{\Omega}{\cdot}cm$ and $1.284{\times}10^{13}{\sim}8.974{\times}10^{13}{\Omega}{\cdot}cm$ at room temperature, respectively. The dielectric constant of the 0y, 40y and 80y were 2.922~3.431, 2.613~3.285 and 2.921~3.332 at room temperature, respectively. It is certain that the ionic ($Na^+$, $Cl^-$, $Mg^{2+}$, ${SO_4}^{2-}$, $Ca^{2+}$, $K^+$) conduction current was formed by the salinity of the seawater. The volume electrical resistivity of the cleaned CSPE via freshwater trends slightly upward with the number of dried days at room temperature. As a result, the $CH_2$ component of thermally accelerated aged CSPE decreased after seawater and freshwater flooding for 5 days respectively, whereas the atoms such as Cl, O, Pb, Al, Si, Sb, S related with the conducting ion ($Na^+$, $Cl^-$, $Mg^{2+}$, ${SO_4}^{2-}$, $Ca^{2+}$, $K^+$) component increased relatively.

• Bulletin of the Korean Chemical Society
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• 제28권2호
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• pp.251-256
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• 2007

The crystal structure of fully dehydrated partially Cs+-exchanged zeolite X, [Cs52Na40Si100Al92O384], a = 24.9765(10) A, has been determined by single-crystal X-ray diffraction techniques in the cubic space group Fd3 at 21 °C. The crystal was prepared by flow method for 5 days using exchange solution in which mole ratio of CsOH and CsNO3 was 1 : 1 with total concentration of 0.05 M. The crystal was then dehydrated at 400 °C and 2 × 10-6 Torr for 2 days. The structure was refined to the final error indices, R1 = 0.051 and wR2 (based on F2) = 0.094 with 247 reflections for which Fo > 4σ (Fo). In this structure, about fifty-two Cs+ ions per unit cell are located at six different crystallographic sites with special selectivity; about one Cs+ ion is located at site I, at the centers of double oxygen-rings (D6Rs), two Cs+ ions are located at site I', and six Cs+ ions are found at site II'. This is contrary to common view that Cs+ ions cannot pass sodalite cavities nor D6Rs because six-ring entrances are too small. Ring-opening by the formation of ?OH groups and ring-flexing make Cs+ ions at sites I, I', and II' enter six-oxygen rings. The defects of zeolite frameworks also give enough mobility to Cs+ ions to enter sodalite cavities and D6Rs. Another six Cs+ ions are found at site II, thirty-six are located at site III, and one is located at site III' in the supercage, respectively. Forty Na+ ions per unit cell are located at two different crystallographic sites; about fourteen are located at site I, the centers of D6Rs and twenty-six are also located at site II in the supercage. Cs+ ions and Na+ ions at site II are recessed ca. 0.34(1) A and 1.91(1) A into the supercage, respectively. In this work, the highest exchange level of Cs+ ions per unit cell was achieved in zeolite X by conventional aqueous solution methods and it was also shown that Cs+ ion could pass through the sixoxygen rings.

• 한국진공학회지
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• 제20권2호
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• pp.155-163
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• 2011

탄소나노튜브(CNT)와 합성기판 사이의 전도성 향상을 목적으로, 현재 리튬이온이차전지 등의 분야에서 전극으로 이용되고 있는 구리 호일을 합성기판으로 하여, 그 위에 수직배향 CNT 성장의 합성 최적화를 도모하였다. 합성은 수평식 CVD 합성장비를 이용하였으며, 최적의 합성조건은 구리호일 위에 10 nm의 Al2O3 버퍼층과 1 nm 두께의 Fe 촉매층을 증착한 후, 아세틸렌 가스를 이용하여 $800^{\circ}C$에서 20분간 합성한 조건으로 설정하였다. CNT는 base-growth의 성장형태를 따랐고, Fe 1 nm 두께인 경우, $7.2{\pm}1.5nm$의 촉매나노입자가 형성되었으며, 이를 이용하여 $800^{\circ}C$에서 20분 성장결과, 직경 8.2 nm, 길이 $325{\mu}m$의 수직배향 CNT를 얻을 수 있었다. 합성시간이 길어져도 CNT의 결정성, 직경 및 겹(wall) 수에는 큰 변화가 없었다. 끝으로, 구리호일 위에 수직 성장시킨 CNT의 전계방출 특성을 측정한 결과, 실리콘 산화막 위에 성장시킨 CNT와 비교하여, 월등히 낮은 전계방출 문턱전압과 10배 정도 높은 전계향상계수를 보였다. 이는 CNT와 금속기판 사이의 계면에서 전기전도도가 향상된 결과에 기인하는 것으로 사료된다.

• 전기화학회지
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• 제16권3호
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• pp.111-122
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• 2013

나트륨 유황전지(NAS)는 대용량 에너지 저장시스템(energy storage system, ESS) 중 하나로서, 최근 풍력에너지, 태양에너지, 해양에너지 등 그린재생에너지의 사용증가로 ESS에 대한 수요가 급증함에 따라 NAS 전지에 대한 관심이 고조되고 있다. NAS 전지는 에너지 밀도가 높고(납 축전지밀도의 3배), 사이클 수명이 길고, 자가방전이 없어 대용량 전력저장 시스템에 적합하다. NAS 전지는 양극으로 황(Sulfur), 음극으로 나트륨(Na), 고체전해질 및 분리막으로 ${\beta}$"-알루미나($Al_2O_3$)로 구성되어 있고, 양극 활물질인 황은 부도체이기 때문에 도전재인 탄소섬유(carbon felt)에 함침시켜 양극으로 사용해야 함으로, 양극재 구성 및 특성은 전지성능에 상당한 영향을 미치게 된다. 따라서 본 논문에서는 NAS 전지의 구성, 다황화나트륨($Na_2S_x$, 방전생성물) 및 양극재의 특성, 전지 성능에 미치는 영향인자들에 대해서 알아보고자 한다.