• 한국대기환경학회지
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• 제2권2호
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• pp.66-74
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• 1986

Rain samples were collected at 10 sites in the Seoul area during the period of August through November, 1985. THe concentrations of the major cations $(H^+, Ca^{++}, MG^{++}, Na^+, K^+, NH_4^+)$ and the major anions $(SO_4^=, NO_3^-, Cl^-)$ were measured to characterize the main sources of chemical ions in rainwater. Correlating concentrations of ions to pH, calculated coefficients ranged from 0.1485 to 0/4296. Sulfate shows the largest coefficient indicating that sulfate is more closely associated with hydrogen ion than other ions. This may suggest that sulfuric acid contributes more to the acidity of rainwater in Seoul. It appears that the major chemicals measured in rainwater are from the anthropogenic sources of air pollution. Predominant chemicals are acidic at the Guro-, the Sinseol-, the Yangnam-, and the Ssangmun-dong with sulfate being the most predominant. IT also indicates that alkaline substances resulting from soil and dust have a significant effect on pH values of rainwater by neutralizing actions. According to Granat-model analysis, it is estimated that the relative contributions to the rainwater acidity in Seoul are 84% from sulfuric acid, 8% from nitric acid and 8% from hydrochloric acid.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2008년도 추계학술대회 논문집
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• pp.51-54
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• 2008

This study aims to devise and analyze a power generation system combining the solid oxide fuel cell and oxy-fuel combustion technology. The fuel cell operates at an elevated pressure, a constituting a SOFC/gas turbine hybrid system. Oxygen is extracted from the high pressure cathode exit gas using ion transport membrane technology and supplied to the oxy-fuel power system. The entire system generates much more power than the fuel cell only system due to increased fuel cell voltage and power addition from oxy-fuel system. More than one third of the power comes out of the oxy-fuel system. The system efficiency is also higher than that of the fuel cell only system. Recovering most of the generated carbon dioxide is major advantage of the system.

• 분석과학
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• 제8권2호
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• pp.139-159
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• 1995

몇 가지 종류의 corticosteroid에 대하여 액체 크로마토그래피-질량분석법으로 양이온 질량 스펙트럼을 얻었다. 화학구조에 따라 수소 첨가된 분자이온 [$MH^+$], 암모늄 첨가이온 [${MNH_4}^+$], 또는 ($MH^+-60$) 이온이 base peak였고 [$MH^+-18$] 또는 [${MNH_4}^+-18$] 이온 등이 특성적으로 나타났다. Methylprednisolone acetate를 male Sprague-Dawley rat에 경구투여한 다음 24시간 동안 배설된 뇨로부터 유리상태 또는 접합상태의 대사물질들을 가수분해, 추출 및 농축하고, thermospray LC/MS를 사용하여 양이온과 음이온 질량토막이온을 분석하였다. Methylprednisolone acetate의 C-21 위치에서의 탈아세틸화(deacetylation), C-20 위치에서 C=0의 -CHOH로의 환원, C-11 위치에서 CHOH의 C=0로의 산화 또는 C-17과 C-20 사이의 bond cleavage등에 의해 생성되는 것으로 추정되는 10여종의 대사물질을 검출하였다. 그 중에 20-hydroxymethylprednisolone(20-HMP), methylprednisolone(MP), methylprednisone(11-KMP)등은 표준물질과 비교 확인하였다.

• 한국식품과학회지
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• 제38권2호
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• pp.169-175
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• 2006

Citrate Iyase(CL)와 oxaloacetate decarboxylase(OD)를 고정화하여 효소 반응기를 제작하고 효소반응으로 생성된 carbonate ion을 ion selective electrode를 이용한 전위차법 FIA system으로 식품에함유된 구연산의 농도를 측정하였다. 최적 센서 시스템의 조건은 CL과 OD을 같이 고정화시키는 방법으로 CL과 OD의 양이 각각 10 units, 60 units, 담체량은 0.3 g, carrier buffer 1(0.1 MTris buffer)은 pH 7.5, carrier buffer의 유속은 12 mL/hr으로 결정되었다. 최적 상태에서의 표준검량곡선은 $10^{-1}\;M-10^{-3}\;M$ 범위에서 직선적인 상관관계$(r^2=0.9986)$를 나타내었다. 당류와 유기산류에 대한 센서 시스템에 대한 방해효과를 측정한 결과 당류는 거의 저해효과를 보이지 않았으며 유기산의 경우도 저해 효과가 5% 미만으로 이들 물질에 의해 감응도가 크게 방해받지 않은 것으로 나타났다. 구연산 바이오센서와 GC를 사용하여 식품 시료에 함유된 구연산의 농도를 분석한 결과 두 방법간에 유의적인 차이가 없는 것으로 나타나 본 연구에서 구축한 구연산 바이오센서 시스템은 식품에 함유된 구연산 분석시 신뢰성 있는 결과를 주는 것으로 보여졌다.

• 대한기계학회논문집A
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• 제38권6호
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• pp.677-682
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• 2014

본 연구에서는 데이터 마이닝의 방법인 의사결정나무와 인공신경망을 이용하여 리튬 이차전지의 전류밀도 특성에 대해 핵심 설계 인자를 도출하고 비교하였다. 먼저 의사결정나무-인공신경망 모델을 이용한 설계방법으로, 비선형성을 나타내는 초기 극판 설계인자들 중에 의사결정나무 모델을 통해 주요 설계 인자를 도출한 다음 인공신경망을 이용하여 설계인자들 간의 중요도와 전류밀도와의 가중치 분석을 수행하였다. 두 번째 방법은 인공신경망 모델만을 이용한 방법으로, 초기 설계인자들을 별도의 주요 인자 도출 과정 없이 모두 인공신경망을 구축하는데 사용하여 전류밀도와의 연관성 및 가중치를 분석하였다.

• 한국표면공학회지
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• 제51권1호
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• pp.47-53
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• 2018

Sn-based lithium-ion batteries have low cost and high theoretical specific capacity. However, one of major problem is the capacity fading caused by volume expansion during lithiation/delithiation. In this study, 3-dimensional foam structure of Cu-Sn alloy is prepared by co-electrodeposition including large free space to accommodate the volume expansion of Sn. The Cu-Sn foam structure exhibits highly porous and numerous small grains. The result of EDX mapping and XPS spectrum analysis confirm that Cu-Sn foam consists of $SnO_2$ with a small quantity of CuO. The Cu-Sn foam structure electrode shows high reversible redox peaks in cyclic voltammograms. The galvanostatic cell cycling performances show that Cu-Sn foam electrode has high specific capacity of 687 mAh/g at a current rate of 50 mA/g. Through SEM observation after the charge/discharge processes, the morphology of Cu-Sn foam structure is mostly maintained despite large volume expansion during the repeated lithiation/delithiation reactions.

• 한국생물환경조절학회:학술대회논문집
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• 한국생물환경조절학회 2003년도 추계학술대회 논문집
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• pp.227-231
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• 2003

• 한국진공학회:학술대회논문집
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• 한국진공학회 2013년도 제44회 동계 정기학술대회 초록집
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• pp.243-244
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• 2013

Over the past 15 years, several groups have incorporated radio-frequency quadrupole (RFQ) based instruments before the accelerator in accelerator mass spectrometry (AMS) systems for ion-gas interactions at low kinetic energy (＜40 eV). Most AMS systems arebased on a tandem accelerator, which requires negative ions at injection. Typically, AMS sensitivity abundance ratios for radioactive-to-stable isotope are limited to Xr/Xs ＞10^-15, and the range of isotopes that can be analyzed is limited because of theneed to produce rather large negative ion beams and the presence of atomic isobaric interferences after stripping. The potential of using low-kinetic energy ion-gas interactions for isobar suppression before the accelerator has been demonstrated for several negative ion isobar systems with a prototype RFQ system incorporated into the AMS system at IsoTrace Laboratory, Canada (Ontario, Toronto). Requisite for any such RFQ system applied to very rare isotope analysis is large transmission of the analyte ion. This requires proper phase-space matching between the RFQ acceptance and the ion beam phase space (e.g. 35 keV, ${\varphi}3mm$, +-35 mrad), and the ability to control the average ion energy during interactions with the gas. A segmented RFQ instrument is currently being designed at Korea Institute for Science and Technology (한국과학기술연구원, KIST). It will consist of: a) an initial static voltage electrode deceleration region, to lower the ion energy from 35 keV down to ＜40 eV at injection into the first RFQ segment; b) the segmented quadrupole ion-gas interaction region; c) a static voltage electrode re-acceleration region for ion injection into a tandem accelerator. Design considerations and modeling will be discussed. This system should greatly lower the detection limits of the 6 MV AMS system currently being commissioned at KIST. As an example, current detection sensitivity of 41Ca/Ca is limited to the order of 10^-15 while the 41Ca/Ca abundance in modern samples is typically 41Ca/Ca~10^-14 - 10^-15. The major atomic isobaric interference in AMS is 41K. Proof-of-principal work at IsoTrace Lab. has demonstrated that a properly designed system can achieve a relative suppression of KF3-/41CaF3- ＞4 orders of magnitude while maintaining very high transmission of the 41CaF3- ion. This would lower the 41Ca detection limits of the KIST AMS system to at least 41Ca/Ca~10^-19. As Ca is found in bones and shells, this would potentially allow direct dating of valuable anthropological archives and archives relevant to our understanding of the most pronounced climate change events over the past million years that cannot be directly dated with the presently accessible isotopes.

• 한국산학기술학회논문지
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• 제19권9호
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• pp.326-332
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• 2018

현재 우리나라는 친환경 및 원전비중 축소라는 에너지 정책의 큰 변화에 직면하고 있다. 그러나 에너지 정책 변화에 따라 폭발적 증가가 예상되는 전기차 배터리 및 에너지저장시스템 등 중대형 이차전지의 폐기물 사후관리체계 및 관련 정책은 매우 미비한 상태이다. 따라서 본 연구는 국내에서 폭발적인 증가가 예상되는 중대형 리튬이온전지의 철거량을 추정해보고, 중대형 이차전지 재활용 산업의 경제성 분석을 실시하고자 한다. 이를 토대로 국내 중대형 이차전지 재활용 산업의 수익성 분석 및 관련 재활용 산업의 활성화를 위한 정책적 대안을 모색하고자 한다. 연구 분석 결과 국내 중대형 리튬이온전지 재활용 사업의 경우 B/C 비율이 1.06으로 편익이 그 비용보다 높아 사업의 경제성이 존재하는 것으로 분석되었다. 동 사업의 경제성이 높고, 현재 국내에 중대형 이차전지 재활용 관련 부분적 원천기술 및 응용기술이 확보되어 있음에도 불구하고 산업 활성화가 되지 않는 이유는 중대형 이차전지 재활용의 법제화가 이루어지지 않아 국내 수요가 낮기 때문인 것으로 분석된다. 따라서 본 연구에서는 생산자책임재활용 제도의 의무대상 품목에 리튬이차전지를 추가하여, 중대형 이차전지 재활용의 국내 수요 확대를 통한 산업 활성화 방안을 제시하였다.

• 한국표면공학회지
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• 제29권5호
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• pp.345-349
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• 1996

The wetting property of polymer surfaces is very important for practical applications. Plasma source ion implantation technique was used to improve the wetting properties of polymer surfaces. Poly(ethylene terephtalate) and other polymer sheets were mounted on the target stage and an RF plasma was generated by means of an antenna located inside the vacuum chamber. High voltage pulses of up to -10kV, 10 $\mu$sec, and up to 1 kHz were applied to the stage. The samples were implanted for 5 minutes with using Ar, $N_2,O_2,CH_4,CF_4$ and their mixture as source gases. A contact angle meter was used to measure the water contact angles of the implanted samples and of the samples stored in ambient conditions after implantation. The modified surfaces were analysed with Time-Of-Flight Mass Spectrometer (TOF-SIMS) and Auger Electron Spectroscopy (AES). The oxygen-implanted samples showed extremely low water contact angles of $3^{\circ}C$ compared to $79^{\circ}C$ of unimplanted ones. Furthermore, the modified surfaces were relatively stable with respect to aging in ambient conditions, which is one of the major concerns of the other surface treatment techniques. From TOF-SIMS analysis it was found that oxygen-containing functional groups had been formed on the implanted surfaces. On the other hand, the $CF_4$-implanted samples turned out to be more hydro-phobic than unimplanted ones, giving water contact angles exceeding $100^{\circ}C$ . The experiment showed that plasma source ion implantation is a very promising technique for polymer surface modification especially for large area treatment.