• 제목/요약/키워드: Elemental ratio

검색결과 252건 처리시간 0.027초

자연토양에서의 소수성 유기오염물질의 느린 흡착 (Slow Sorption of Hydrophobic Organic Contaminants in Natural Soils)

  • 신원식;박대효;안태봉;천희동
    • 한국지반환경공학회 논문집
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    • 제2권1호
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    • pp.103-114
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    • 2001
  • 본 연구에서는 근래에 퇴적된 습지토양의 유기물질에 느린 흡착부분이 존재하는지 살펴보기 위해 흡착실험을 행하였다. 최근 퇴적된 민물 습지토양에서의 소수성 유기화합물 (chlorobenzene and phenanthrene)의 흡착 특성을 회분식 흡착법을 사용하여 결정하였다. 유기물질의 나이의 상대 척도로서 산소/탄소 원소비 등을 포함한 여러 방법으로서 평가하였다. 토양의 나이가 유기화합물의 습지토양에서의 흡착에 차이를 유발하는지에 대해 조사하기 위하여 습지 토양의 표층부(상층부 0-2cm, 5년 미만)과 하층부(below 10cm, 20년 이상)에 대한 느린 흡착 특성을 상대적으로 오래된 PPI(Petro Processors, Inc. Superfund site), BM(Bayou Manchac) 토양과 비교하였다. 느린 흡착모델 변수의 비선형성(KF와 N)의 증가로서 느린 흡착부분이 존재함을 알 수 있었다. 느린 흡착모델의 분석결과 상당한 크기의 느린 흡착부분이 존재하였으며 습지 토양의 경우 흡착된 chlorobenzene의 25.4-263%가 phenanthrene의 경우 흡착된 양의 1.4-1.9%(phenanthrene)가 각각 느린 흡착 부분에 해당하였으며, PPI 토양과 BM토양의 경우 흡착된 chlorobenzene의 40.0-55.93%와 흡착된 phenanthrene의 2.9-3.19%가 각각 느린 흡착 부분에 해당하였다. 느린 흡착 부분은 상층부 < 하층부 < PPI < BM 토양의 순으로 증가하였는데 이것은 토양 유기물질의 나이가 증가할수록 느린 흡착부분의 크기가 증가함을 나타낸다.

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Hydroxylapatite 및 Titanium Plasma Spray 피복임프란트와 골조직 계면의 조직학적 비교 연구 (HISTOLOGIC COMPARATIVE STUDY ON THE BONE-IMPLANT INTERFACE OF HYDROXYLAPATITE AND TITANIUM PLASMA SPRAY COATED IMPLANTS)

  • 조주온;송광엽;박찬운
    • 대한치과보철학회지
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    • 제33권3호
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    • pp.492-516
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    • 1995
  • This study evaluated the responses of mandibular bones of mongrel dogs to loaded hydro xylapatite(HA) and titanium plasma spray(TPS) coated endosseous dental implants, using unloaded ones as the control group. after HA and TPS coated implants were implanted, their bone reactions with vital bones have been observed with light and scanning electron microscope(SEM) at the three periods of the 4th, 12th and 20th week. These reactions have been also compared in a histomorphometric method. The elemental distribution state of implants and the interface neighboring bone tissues have been measured with the energy dispersive analysis of X-rays(EDAX). The following results were obtained ; 1. The light microscopic analysis showed osseointegration in both the control group and the occlusal force loaded group ; Its degree was shown to be higher in the long-maintained and occlusal force groups. 2. The SEM analysis showed that both groups had osseointegration, In the case of TPS-coated implants, the coated layer was divided on the bone interface. In the case of HA-coated implants, there appeared a division between the metal and coated interface. 3. In the histomorphometric analysis, the measured ratio contaction bone of TPS-coated implants was $70{\pm}19$% in the case of no occlusal force ; it was $84{\pm}13$% in the case of occlusal force. The measured ratio contacting bone of HA-coated implants was $75{\pm}18$% in the case of no occlusal force ; it was $94{\pm}9$% in the case of occlusal force. However, there was no significant difference statistically(p>0.05). 4. Both groups showed that the ratio of calcium and phosphorous increased more in the bone tissues than on the bone to implant interface.

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물-암석반응에 따른 물에서의 Sr동위원소의 거동에 대한 예비실험결과 (Preliminary Experimental Result for Clarifying Sr Isotope Behaviour of Water due to Water-Rock Interaction)

  • 이승구;김정찬
    • 자원환경지질
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    • 제43권3호
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    • pp.211-222
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    • 2010
  • 물-암석 반응에 따른 물속의 Sr의 농도와 $^{87}Sr/^{86}Sr$ 비의 변화를 조사하기위해 실온에서의 회분식 실험(batch experiment)을 수행하였다. 실험방법은 기원이 서로 다른 2종류 화강암(강화 석모도 흑운모 화강암과 포천 석류석 화강암), 증류수, 지표수를 사용하여 암석을 증류수 및 지표수와 1:1의 비율로 각각 반응시킨 후의 물속의 양이온 및 음이온의 농도변화 및 물속의 $^{87}Sr/^{86}Sr$ 비를 측정하였다. 그리고 암석과 지표수의 경우, 혼합비의 차이에 의한 비교를 위해 암석과 지표수의 비율을 1:10으로 하여 반응시킨 후의 물속의 양이온과 양이온의 농도변화 및 $^{87}Sr/^{86}Sr$ 비를 측정하였다. 연구결과에 의하면, 물속의 용존성분의 함량은 초기 3-4개월간은 증가하였지만, 1년간 방치하여 놓은 시료에서는 함량이 현저하게 줄어들었다. 반면에 물속의 $^{87}Sr/^{86}Sr$ 비는 시간의 경과와 더불어 암석의 $^{87}Sr/^{86}Sr$ 비로 이동해가면서 비교적 안정되는 경향을 보여주었다. 이는 물-암석반응에 의한 물속의 $^{87}Sr/^{86}Sr$ 비는 거의 거의 평형에 도달한 이후에는 Sr 함량이나 기타 용존이온들보다 쉽게 안정됨을 지시해주는 것으로 볼 수 있다. 이 연구결과는 서로 다른 대수층에 분포하는 지하수의 연계성 혹은 혼합비를 계산하는데 있어서 $^{87}Sr/^{86}Sr$ 비가 유용하게 활용되어 질 수 있음을 지시해준다.

Poly(1,4-bis((E)-2-(3-dodecylthiophen-2-yl)vinyl)benzene) for Solution Processable Organic Thin Film Transistor

  • Kim, Chul-Young;Park, Jong-Gwang;Lee, Min-Jung;Kwon, Soon-Ki;Kim, Jin-Hak;Shin, Sung-Chul;Kim, Yun-Hi
    • Bulletin of the Korean Chemical Society
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    • 제33권5호
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    • pp.1659-1663
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    • 2012
  • New semiconducting polymer, poly[1,4-bis(($E$)-2-(5-bromo-3-dodecylthiophen-2-yl)vinyl)benzene], was designed, synthesized and characterized. The structure of polymer was confirmed by $^1H$-NMR, IR and elemental analysis. The polymer was soluble in specific organic solvent. The weight-average molecular weights (MW) of polymer was found to be 11,000 with polydispersity of 1.82. UV-Visible absorption spectrum showed the maximum absorption at 428 nm (in solution) and 438 nm (in film). The highest occupied molecular orbital (HOMO) energy of the polymer is -5.36 eV by measuring cyclic voltammetry (CV). A solutionprocessed polymer thin film transistor device shows a mobility of $8.59{\pm}10^{-4}\;cm^2\;V^{-1}\;s^{-1}$, an on/off current ratio of $2.0{\times}10^4$.

Structural and Electrical Features of Solution-Processed Li-doped ZnO Thin Film Transistor Post-Treated by Ambient Conditions

  • Kang, Tae-Sung;Koo, Jay-Hyun;Kim, Tae-Yoon;Hong, Jin-Pyo
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2012년도 제43회 하계 정기 학술대회 초록집
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    • pp.242-242
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    • 2012
  • Transparent oxide semiconductors are increasingly becoming one of good candidates for high efficient channel materials of thin film transistors (TFTs) in large-area display industries. Compare to the conventional hydrogenated amorphous silicon channel layers, solution processed ZnO-TFTs can be simply fabricated at low temperature by just using a spin coating method without vacuum deposition, thus providing low manufacturing cost. Furthermore, solution based oxide TFT exhibits excellent transparency and enables to apply flexible devices. For this reason, this process has been attracting much attention as one fabrication method for oxide channel layer in thin-film transistors (TFTs). But, poor electrical characteristic of these solution based oxide materials still remains one of issuable problems due to oxygen vacancy formed by breaking weak chemical bonds during fabrication. These electrical properties are expected due to the generation of a large number of conducting carriers, resulting in huge electron scattering effect. Therefore, we study a novel technique to effectively improve the electron mobility by applying environmental annealing treatments with various gases to the solution based Li-doped ZnO TFTs. This technique was systematically designed to vary a different lithium ratio in order to confirm the electrical tendency of Li-doped ZnO TFTs. The observations of Scanning Electron Microscopy, Atomic Force Microscopy, and X-ray Photoelectron Spectroscopy were performed to investigate structural properties and elemental composition of our samples. In addition, I-V characteristics were carried out by using Keithley 4,200-Semiconductor Characterization System (4,200-SCS) with 4-probe system.

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Development of Near-Critical Water Reaction System for Utilization of Lignin as Chemical Resources

  • 엄희준;홍윤기;박영무;정상호;이관영
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2010년도 춘계학술대회 초록집
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    • pp.251.2-251.2
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    • 2010
  • Plant biomass has been proposed to be an alternative source for petroleum-based chemical compounds. Especially, phenolic chemical compounds can be obtained from lignin by chemical depolymerization processes because lignin consists of complex aromatic polymer such as trans-p-coumaryl, coniferyl and sinapyl alcohols, etc. Phenolic chemical compounds from lignin were usually produced in super critical water. However, we applied Near-critical water (NCW) system because NCW is known as a good solvent for lignin depolymerization. Organic matter like lignin can be solved in NCW system and the system has a unique acid-base property without conventional non-eco-friendly chemicals such as sulfuric acid and sodium hydroxide. In this work, we tried to optimize the NCW depolymerization system by adjusting the processing variables such as reaction time, temperature and pressure. Moreover, the amount of additional phenol was optimized by changing the molar ratio between water and phenol. Phenol was used as capping agent to prevent re-polymerization of active fragment such as formaldehyde. Alkali-lignin was used as a starting material and characterized by a Solid State 13C-NMR, FT-IR and EA (Elemental Analysis). GC-MS analysis confirmed that o-cresol, p-cresol, anisole and 4-hydroxyphathalic acid were the main product and they were quantitatively analyzed by HPLC.

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Preparation and Characterizations of C60/Polystyrene Composite Particle Containing Pristine C60 Clusters

  • Kim, Jung-Woon;Kim, Kun-Ji;Park, Soo-Yeon;Jeong, Kwang-Un;Lee, Myong-Hoon
    • Bulletin of the Korean Chemical Society
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    • 제33권9호
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    • pp.2966-2970
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    • 2012
  • Fullerene/polystyrene ($C_{60}$/PS) nano particle was prepared by using emulsion polymerization. Styrene and fullerene were emulsified in aqueous media in the presence of poly(N-vinyl pyridine) as an emulsion stabilizer, and polymerization was initiated by water soluble radical initiator, potassium persulfate. The obtained nano particles have an average diameter in the range of 400-500 nm. The fullerene contents in the nano particle can be controlled up to 15 wt % by varying the feed ratio, which was confirmed by themogravimetric analysis (TGA) and elemental analysis (EA). The structure and morphologies of the $C_{60}$/PS nano particles were examined by various analytical techniques such as dynamic light scattering (DLS), scanning electron microscope (SEM), transmission electron microscope (TEM), electron diffraction (ED) pattern, X-ray powder diffraction (XRD), and UV spectroscopy. Unlike conventional $C_{60}$/PS particles initiated by organic free radical initiators, in which the fullerene is copolymerized forming a covalent bond with styrene monomer, the prepared $C_{60}$/PS nano particles contain pristine fullerene as secondary particles homogeneously distributed in the polystyrene matrix.

Catalytic hydrogenation-assisted preparation of melt spinnable pitches from petroleum residue for making mesophase pitch based carbon fibers

  • Lee, Dong Hun;Choi, Jisu;Oh, Young Se;Kim, Yoong Ahm;Yang, Kap Seung;Ryu, Ho Jin;Kim, Yong Jung
    • Carbon letters
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    • 제24권
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    • pp.28-35
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    • 2017
  • We demonstrated an effective way of preparing melt spinnable mesophase pitches via catalytic hydrogenation of petroleum residue (fluidized catalytic cracking-decant oil) and their subsequent thermal soaking. The mesophase pitches thus obtained were analyzed in terms of their viscosity, elemental composition, solubility, molecular weight, softening point and optical texture. We found that zeolite-induced catalytic hydrogenation under high hydrogen pressure contributed to a large variation in the properties of the pitches. As the hydrogen pressure increased, the C/H ratio decreased, and the solubility in n-hexane increased. The mesophase pitch with entirely anisotropic domains of flow texture exhibited good meltspinnability. The mesophase carbon fibers obtained from the catalytically hydrogenated petroleum residue showed moderate mechanical properties.

불소 도핑 이산화주석 박막의 수소플라즈마 내구성 (HYDROGEN PLASMA DURABILITY OF $SnO_2$:F FILMS)

  • 윤경훈;송진수;강기환
    • 대한전기학회:학술대회논문집
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    • 대한전기학회 1992년도 하계학술대회 논문집 B
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    • pp.847-849
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    • 1992
  • Fluorine-doped ($SnO_2$:F) thin films obtained by pyrosol deposition method have been exposed to R.F. excited pure hydrogen plasma under the following conditions; substrate temperature of 200$^{\circ}C$, $H_2$ pressure of 1 Torr, R.F. input power of 50 mW/$\textrm{cm}^{2}$, $H_2$ flow rate of 30cc/min and exposure time of 15-600 seconds. It is found that the sheet resistance of the films remains unchanged or rather slightly reduces for initial exposure time of 30-60 seconds, but increases sharply with further increasing the exposure time. The optical transmittance of $SnO_2$:F films slows a rapid fall with increasing exposure time except for a film obtained with a solution having $CH_3OH/H_2O$ mol ratio of 2.65, its degradations at the exposure time of 30-60 seconds are about 7-15%. In addition, the exposure of the films to hydrogen plasma atmosphere leads to remarkable changes in the microstructure and chemical composition, which should be attributed to the reduction of $SnO_2$ to SnO and to elemental Sn.

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R&D ACTIVITIES FOR PARTITIONING AND TRANSMUTATION IN KOREA

  • Yoo, Jae-Hyung;Song, Tae-Young
    • 한국방사성폐기물학회:학술대회논문집
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    • 한국방사성폐기물학회 2004년도 Proceedings of the 4th Korea-China Joint Workshop on Nuclear Waste Management
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    • pp.150-164
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    • 2004
  • According to the Korean long-term plan for nuclear technology development, KAERI is conducting a few R&D projects related to the proliferation-resistant back-end fuel cycle. The R&D activities for the back-end fuel cycle are reviewed in this work, especially focusing on the study of the partitioning and transmutation(P&T) of long-lived radionuclides. The P&T study is currently being carried out in order to develop key technologies in the areas of partitioning and transmutation. The partitioning study is based on the development of pyroprocessing such as electrorefining and electrowinning because they can be adopted as proliferation-resistant technologies in the fuel cycle. In this study, various behaviors of the electrodeposition of uranium and rare earth elements in the LiCl-KCl electrorefining system have been examined through fundamental experimental work. As for the transmutation system, KAERI is studying the HYPER (HYbrid Power Extraction Reactor), a kind of subcritical reactor which will be connected with a proton accelerator. Up to now, a conceptual study has been carried out for the major elemental systems of the subcritical reactor such as core, transuranic fuel, long-lived fission product target, and the Pb-Bi cooling system, etc. In order to enhance the transmutation efficiency of the transuranic elements as well as to strengthen the reactor safety, the reactor core was optimized by determining its most suitable subcriticality, the ratio of height/diameter, and by introducing the concepts of optimum core configuration with a transuranic enrichment as well as a scattered reloading of the fuel assemblies.

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