• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 2009.11a
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• pp.247-247
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• 2009

반도체 집적회로의 고질적화와 고성능화를 위한 기본소자의 미세화 및 단위공정의 개선이 필요하다. 이를 위해서 본 연구에서는 자기조립특성을 가지는 DNA분자를 형틀로 이용한 황화구리 나노선의 합성 및 배열기술을 연구하였다. DNA 나노구조물을 기반으로 다양한 형태의 나노구조물 형성이 가능하다는 장점과 반도체성 물질인 황화구리와의 결합 특성을 이용하여 나노선 및 나노소자를 제작하는 기술을 확보하였다.

• Proceedings of the Korea Air Pollution Research Association Conference
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• 2003.11a
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• pp.283-284
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• 2003

환원황 성분들은 사람들이 일상적으로 생활하는 환경권역에서 고농도 (ppb 수준 이상)로 존재할 경우, 악취의 주요원인물질로 작용한다는 점에서 상당한 주목을 받고 있다. 국내의 경우, 환경부에서는 이미 '92년 8월 대기환경보전 법을 개정하여, 황화수소를 위시한 4개의 황화합물과 트리메틸아민, 암모니아, 아세트알데히드, 스티렌을 포함하는 총 8개 화합물을 악취물질로 지정하여 관리하고 있다. 이러한 황화합물을 분석하는데 spectrophotometry, polarography, fluorescence, coulometry, impregnated filter 방식 등이 활용되고 있다 (Blank et al., 1978). (중략)

• Journal of the Mineralogical Society of Korea
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• v.19 no.3 s.49
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• pp.139-151
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• 2006

Base metal sulfides occur in the Huronian sedimentary rocks that cover the Archean volcanic rocks in the Cobalt area, Ontario, Canada. They are mostly concentrated in the basal conglomerate which was formed in the pre-Huronian basin structure. Sulfide occurrence can be grouped as massive sulfide clasts in the basal and Coleman conglomerate, disseminated sulfides throughout the sediments, and disseminated sulfides near Ag-Co-Ni-As carbonate veins. Detrital mechanism can explain features such as angularity of sulfide fragments and graded bedding of dissemnated sulfides. Sulfides concentrated near carbonate veins are probably of hydrothermal origin. Nearby strata-bound type massive sulfide ore deposits and mineralized interflow units are the most probable sources for syngenetic sulfides. This is supported by the angularity of sulfide fragments, presence of massive sulfide boulders which are identical in mineralogy and texture to the strata-bound type sulfide deposits in the Archean basement, and a similar composition of sphalerite in the Archean volcanic rocks and Huronian sedimentary rocks. Some sulfide grains, especially in sandstones and argillites, were undergone recrystallization during the intrusion of the Nipissing diabase.

• Journal of Oral Medicine and Pain
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• v.22 no.2
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• pp.233-239
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• 1997

현대사회에서 구취의 유무가 가정 및 사회생활을 유지하는데 중요한 문제로 대두됨에 따라 구취의 예방과 치료에 관심이 증대되고 있다. 많은 연구자들에 의해 구취에 관한 연구가 이루어지고 있으며, 특히 구취의 연구에서는 객관적이며 정확한 구취의 측정이 중요한 과제가 되고 있다. 이에 저자들은 건강한 구강조직을 가진 서울대학교 치과대학생 및 치과병원 종사자 21명을 대상으로 시각차에 대한 실험, 구강세정에 대한 실험, 구강내로 삽입되는 straw의 구강내 위치에 대한 실험, straw의 종류에 대한 실험 및 구강내 타액의 양에 대한 실험을 실시한 결과 아래와 같은 결론을 얻었다. 1. 휘발성 황화합물의 농도는 하루중 기상직후 식사나 잇솔질하기 전에서 가장 높았다. 2. 잇솔질과 zinc chloride 양치후 휘발성 황화합물 농도의 유의한 감소를 보였다(p<0.05). 3. 측정시 straw가 구강내로 들어가는 깊이가 줄어들수록 휘발성 황화합물의 농도가 유의하게 감소하였다. (p<0.05). 4. 측정에 사용된 straw의 종류는 휘발성 황화합물의 농도에 영향을 주지 않았다. 5. 구강내에 타액을 머금고 측정했을 매 휘발성 황화합물 농도의 유의한 감소가 관찰되었고(p<0.05), 숨을 쉬지않고 측정했을 때는 변화가 관찰되지 않았다 6. 구취 측정시 개구정도에 따른 측정값의 유의한 차이는 관찰되지 않았다.

• Journal of Environmental Health Sciences
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• v.17 no.1
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• pp.39-49
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• 1991

고온에서 황화수소(H$_{2}$S)를 제거하기 위한 흡착제를 개발할 목적으로 ZnO에 $Fe_{2}O_{3}$를 5~50 atomic %까지 첨가시켜 제조한 다공성 흡착제와 황화수소와의 반응(sulfidation)을 thermogravimetric analyzer (Shimadzu DT-30)로 수행하였으며, 고정층세서 zinc ferrite 흡착제의 흡착능을 측정하였다. 반응온도는723$^{\circ}$K~973$^{\circ}$K범위이며, 반응기체는 황화수소(2vol.%)와 질소와 혼합기체로서 total gas flow rate는 200ml/min으로 고정시켰다. Grain Model을 사용하여 실험데이터를 분석한 결과 전화율이 낮을 때 zinc ferrite와 황화수소 반응의 율속단계는 화학반응이었고 황화수소 농도에 대해 1차 반응이었다. 실험한 흡착제 중 10 atomic %의 $Fe_{2}O_{3}$를 첨가하여 제조한 zinc ferrite형 흡착제가 반응속도, 흡착능, 그리고 재생성면에서 우수한 흡착제로 밝혀졌다.

• Transactions of the Korean hydrogen and new energy society
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• v.32 no.6
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• pp.612-617
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• 2021

In the case of a metal sulfide electrode, it is used as an anode or cathode active material in a lithium battery. The reason is that the voltage exists between 0.8 and 2.0 V via lithium electrode and the discharge and charge capacity is high. In order to manufacture nickel sulfide for electrode, which are widely used, nano-nickel powder was sulfided using ammonium polysulfide, and single-phase NiS electrodes were manufactured through heat treatment. The prepared NiS electrode had a high initial capacity of 500 mAh/g or more, and was stabilized after 20 cycles to maintain a capacity of 400 mAh/g or more until 100 cycles.

• Horticultural Science & Technology
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• v.33 no.2
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• pp.210-218
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• 2015

Melon leaves showing yellowing symptoms were analyzed using electron microscopy and RT-PCR for major cucurbit-infecting-viruses (CMV, MNSV, CGMMV, SqMV, WMV, KGMMV, PRSV and ZYMV) reported in Korea, but these viruses were not detected. As the result of further analysis by next-generation sequencing (NGS), the virus was identified as Cucurbit aphid-borne yellows virus (CABYV), and then confirmed by RT-PCR using CABYV-specific primers. When photosynthetic capacity was measured based on chlorophyll fluorescence yield (ChlFY), the leaves of the diseased plants showed $4.09{\mu}mol{\cdot}m^{-2}{\cdot}s^{-1}$, which was one-third of the readings observed for unaffected normal plants ($12.36{\mu}mol{\cdot}m^{-2}{\cdot}s^{-1}$). The root functions of plants affected by leaf yellowing symptoms (LYS) was $0.28mg{\cdot}g^{-1}$, about half that measured for the normal unaffected plants ($0.48mg{\cdot}g^{-1}$). Cytological observations revealed that there were no morphological differences in the palisade parenchyma and mesophyll spongy cells of the leaves between the diseased and the normal plants. However, the same leaf cells of the affected plants contained more starch granules compared to those of the normal, unaffected plants. We conclude that the LYS of muskmelon is not merely a physiological disorder but a viral disease caused by CABYV and spread by aphids.

• Journal of Korean Society of Environmental Engineers
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• v.31 no.11
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• pp.965-974
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• 2009

This study evaluated the degradation efficiency of malodorous sulfurized-organic compounds by utilizing N- and Sdoped titanium dioxide under visible-light irradiation, and examined the catalyst deactivation and regeneration. Catalyst surface was characterized by employing Fourier-Transform-Infrared-Red (FTIR) spectra. The visible-light-driven photocatalysis techniques were able to efficiently degrade low-level dimethyl sulfide (DMS) and dimethyl disulfide (DMDS) with degradation efficiencies exceeding 97%, whereas they were not effective regarding the removal of high-level DMS and DMDS, with degradation efficiencies of 84 and 23% within 5 hrs of photocatalytic processes. As compared with DMS, DMDS which containes one more sulfur element revealed quick catalyst deactivation. Catalyst deactivation was confirmed by the equality between input and output concentrations of DMD or DMDS, the obsevation of no $CO_2$ generation during a photocatalytic process, and the FTIR spectrum peaks related with sulfur ion compounds, which are major byproducts formed on catalyst surfaces. The mineralization efficiency of DMS at 8 ppm, which was a peak value during a photocatalytic process, was calculated as 144%, exceeding 100%. The catalyst regenerated by high-temperature calcination exhibited higher catalyst recovery efficiency (53 and 58% for DMDS and DMS, respectively) as compared with dry-air and humid-air regeneration processes. However, even the calcined method was unable to totally regenerate deactivated catalysts.

• Korean Chemical Engineering Research
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• v.51 no.5
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• pp.568-574
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• 2013

A semi-pilot biofilter packed with media with immobilized Thiobacillus sp. IW and return sludge, was operated under various operating conditions in order to treat malodorous waste air containing both hydrogen sulfide and ammonia which are major air pollutants emitted from composting factories and many publicly owned treatment works (POTW). At the incipient and middle stages of a semi-pilot biofilter operation, the hydrogen sulfide-removal efficiency behaves regardless of an inlet-load of ammonia. However, the ammonia-removal efficiency decreased as an inlet-load of hydrogen sulfide increased. Nevertheless, at the final stage of the semi-pilot biofilter operation, the ammonia-removal efficiency was not affected by the increase of hydrogen sulfide-inlet load. It is attributed to that a serious acidification of semi-pilot biofilter-media did not occur due to continuous injection of buffer solution at the final stage of the semi-pilot biofilter operation. When both hydrogen sulfide and ammonia contained in malodorous waste air were treated simultaneously by semi-pilot biofilter, the maximum elimination capacities of hydrogen sulfide and ammonia turned out to be ca. 58 and $30g/m^3/h$, respectively. These maximum elimination capacities were estimated to be ca. 39 and 46% less than those for lab-scaled biofilter-separate elimination of hydrogen sulfide and ammonia, respectively. Thus, for the simultaneous biofilter-treatment of hydrogen sulfide and ammonia, the maximum elimination capacity of ammonia decreased by 7% more than that of hydrogen sulfide.

• Tribology and Lubricants
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• v.26 no.6
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• pp.317-321
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• 2010

Thin films of tin sulphide (SnS) have been formed by a novel 2-stage process where-in D.C. magnetron sputtering was used to deposit to thin films of tin (Sn) and the layers then sulphidised using 5% hydrogen sulphide ($H_2S$) gas in Argon. Although it was not found possible to deposit high quality thin films of tin directly onto glass substrates, excellent layers of tin were produced by using molybdenum (Mo) coated glass as the substrate material. The chemical and physical properties of the SnS layers formed were determined using scanning electron microscopy, energy dispersive x-ray analysis, x-ray diffraction studies and using reflectance versus wavelength measurements and these related to the conditions of synthesis. The data shows that it should be possible to produce conventional "substrate structure" devices based on the use of this technology.