• 한국축산시설환경학회지
• /
• 제19권2호
• /
• pp.177-182
• /
• 2013

We studied the possibility to produce solid fuel using cattle manure and to apply TAO (Thermophilic Aerobic Oxidation) process of solid-liquid separation fraction. The physiochemical compositions of cattle manure solid fuel chip were analyzed as water 0.12%, low calorific value 3,510 kcal/kg, ashes 11.9%, chlorine 0.82%, sulfur dust 0.5%, mercury non-detection, cadmium 1.0 mg/kg, lead 2 mg/kg, arsenic non-detection. In treating cattle manure with TAO reactor the internal temperature of the reactor was increasing higher and $50^{\circ}C$ and over was maintained after 20 hours on. The physiochemical compositions of liquids increased from pH 7.3 to pH 9.18 and EC decreased from 4.6 to 3.48 mS/cm in treating process of cattle manure with TAO reactor. COD and SCOD decreased from 16,800 to 10,400 mg/L, from 4,600 to 2,040 mg/L respectively, which showed about 38% and 56% of remove efficiency respectively.

• 대한화학회지
• /
• 제38권2호
• /
• pp.146-150
• /
• 1994

1.000%(w/v)텅스텐 메트릭스 중에 미량불순물로 존재하는 아연, 카드뮴, 납 및 구리의 동시정량을 펄스차이 벗김전압전류법으로 검토하였다. 지지전해질로는 타르타르산(pH=5.00)을 사용하였다. 사전 농축은 -1.2 volt(vs. Ag/AgCl)에서 3분간이면 충분하였다. 1.000%(w/v)텅스텐 매트릭스 중에서 아연, 카드뮴, 납 및 구리 각 원소의 동시 정량이 가능한 직선 범위는 10 ~ 50 ppb였으며, 3${\sigma}$검출한계는 각각 1.25, 1.02, 1.69, 1.02ppb 로 나타났다. 이 결과는 텅스텐 매트릭스하에서 ICP-AES의 검출한계인 8.0, 5.0, 120, 5 ppb 결과와 비교하여 볼때, 본 방법이 보다 우수한 미량분석방법임을 알 수 있다.

• 상하수도학회지
• /
• 제30권6호
• /
• pp.673-682
• /
• 2016

In this study, we investigated influent and effluent water pollutants in 53 Public Sewage Treatment Works (PSTWs) where industrial wastewater or landfill leachate is combined four times for two years from 2014 to 2015. Also, we analyzed the characteristics of heavy metals and volatile organic carbons at influent and effluent of these PSTWs caused by sewage treatment combined with industrial wastewater or landfill leachate. As a result, six heavy metals such as barium, copper, iron, manganese, nickel and zinc, and four volatile organic carbons (VOCs) including phenols, di(2-)ethylhexyl phthalate (DEHP), formaldehyde and toluene were observed above detection limits in most of PSTWs. Also, it was revealed that six heavy metals such as hexavalent chromium, mercury, cadmium, chromium, nickel and selenium, and four VOCs including 1,1-dichloroethylene, vinyl chloride, naphthalene, and epichlorohydrin were observed more frequently according to precipitation. As a result of reviewing the monitoring data on "Water Quality Monitoring Networks" in lower watersheds of PSTWs, both heavy metals and VOCs were below detection limits, indicating that the effluent water had little influence on the watershed. Nevertheless for the better management of influent and effluent pollutants in PSTWs, it is necessary to establish the advanced management plans for water pollutants in PSTWs, which include a list of priority substances management, monitoring plans, and guidelines for industrial wastewater and landfill leachate combined in PSTWs.

• 우주기술과 응용
• /
• 제1권1호
• /
• pp.49-63
• /
• 2021

태양계 천체 탐사는 다양한 탑재체를 통해 이루어지고 있고, 그에 따라 많은 연구 결과들이 나오고 있다. 우리는 태양계 천체 연구의 한 방법으로 딥러닝 적용을 시도해 보았다. 지구 관측 위성 자료와 다르게 태양계 천체 자료들은 천체들에 따라 탐사선에 따라 각 탐사선의 탑재체에 따라 그 자료의 형태가 매우 다르다. 그래서 학습시킨 모델로 다양한 자료에 적용이 어려울 수 있지만 사람에 의한 오류를 줄이거나, 놓치는 부분들을 보완해 줄 수 있을 것이라고 기대한다. 우리는 달 표면의 크레이터를 탐지하는 모델을 구현해 보았다. Lunar Reconnaissance Orbiter Camera (LROC) 영상과 제공하는 shapefile을 입력값으로 하여 모델을 만들었고, 이를 달 표면 영상에 적용하여 보았다. 결과가 만족스럽지는 못했지만 이후 이미지 전처리와 모델 수정 작업을 통해 최종적으로는 ShadowCam에 의해 획득되는 달의 영구음영지역 영상에 적용할 예정이다. 이 외에도 달 표면과 비슷한 형태를 가진 세레스와 수성에 적용을 시도하여 딥러닝이 태양계 천체 연구에 또 다른 방법임을 시사하고자 한다.

• 분석과학
• /
• 제10권3호
• /
• pp.216-224
• /
• 1997

순환 전압-전류 그림에서 루비안산의 전기화학적 행동을 조사해 보면, 루비안산은 두 개의 환원 봉우리가 나타나는데, 첫번째 봉우리는 $S^{2-}$ 봉우리와 일치하므로 HgS 생성에 의한 환원 봉우리이며, 두번째 봉우리는 매우 약하며 확인되지 않았다. 시차 펄스 음극 벗김 전압-전류법으로 미량의 루비안산을 정량하는 방법을 고찰하였다. 루비안산의 정량을 위하여 pH 10.0, 붕산염 완충용액을 사용하였고, 최적 조건은 붕산염 완충용액의 농도 0.05M, 축적전위 -0.30V, 축적시간 120초, 그리고 주사속도 10mV/sec이다. 이 때 루비안산의 검출 한계는 $2.7{\times}10^{-8}M$이다.

• Toxicological Research
• /
• 제29권3호
• /
• pp.211-215
• /
• 2013

The trace toxic metal copper was assayed using mercury immobilized on a carbon nanotube electrode (MCW), with a graphite counter and a reference electrode. In this study, a macro-scale convection motor was interfaced with a MCW three-electrode system, in which a handmade MCW was optimized using cyclic- and square-wave stripping voltammetry. An analytical electrolyte for tap water was used instead of an expensive acid or base ionic solution. Under these conditions, optimum parameters were 0.09 V amplitude, 40 Hz frequency, 0.01 V incremental potential, and a 60-s accumulation time. A diagnostic working curve was obtained from 50.0 to 350 ${\mu}g/L$. At a constant Cu(II) concentration of 10.0 ${\mu}g/L$, the statistical relative standard deviation was 1.78% (RSD, n = 15), the analytical accumulation time was only 60 s, and the analytical detection limit approached 4.6 ${\mu}g/L$ (signal/noise = 3). The results were applied to non-treated drinking water. The content of the analyzed copper using 9.0 and 4.0 ${\mu}g/L$ standards were 8.68 ${\mu}g/L$ and 3.96 ${\mu}g/L$; statistical values $R^2$ = 0.9987 and $R^2$ = 0.9534, respectively. This method is applicable to biological diagnostics or food surveys.

• 한국환경과학회지
• /
• 제22권10호
• /
• pp.1273-1278
• /
• 2013

Novel rhodamine 6G fluorescent chemosensors 1 and 2 for the detection of transition metal cations were synthesized through the condensation of rhodamine 6G ethylenediamine with each of 2-hydroxy-1-naphthaldehyde and 2,6-pyridinedicarbaldehyde, respectively. 1 and 2 were characterized using $^{13}C$ NMR, $^1H$ NMR and mass spectroscopy. Fluorometric and colorimetric measurements involving various metal ions revealed the ring opening of the rhodamine 6G spirocycle framework. In the absence of metal cations, 2 was colorless and non-fluorescent, whereas the addition of metal cations ($Hg^{2+}$ and others) changed the color to pink, accompanied by the appearance of an orange fluorescence. The chemosensors exhibited high selectivity for $Hg^{2+}$ over other divalent first-row transition metals. The complexes of $Hg^{2+}$ with 1 and 2 were successfully isolated. A huge enhancement in the fluorescence for both one- and two-photon excitations makes these compounds suitable candidates to be used for fluorescent labeling of biological systems.

• 대한화학회지
• /
• 제35권5호
• /
• pp.506-511
• /
• 1991

In-Morin 착물에 대한 흡착벗김전압전류법적 연구를 HMDE를 사용하여 pH 3.20의 0.1M 아세테이트 완충용액에서 수행하였다. 흡착 현상들을 미분펄스전압전류법으로 관찰하였으며, HMDE의 표면에 흡착된 착물의 환원 전류에 미치는 여러 분석 조건들에 과하여 논의하였다. 또한 여러 다른 금속이온들과 계면활성제의 방해효과에 관해서도 검토하였다. 본 연구에서의 검출한계는 90초의 흡착시간을 적용하였을 때 2.6nM이었으며, 4${\mu}g$/l의 In을 7회 분석하였을 때 상대표준편차는 2.0%이었다.

• 대한화학회지
• /
• 제32권2호
• /
• pp.130-134
• /
• 1988

수은방울전극에서 바로 시안이온을 시차펄스음극벗김 전압전류 법으로 측정한 결과 검출한계를 낮출수가 있었다. 가장 알맞는 실험조건은 다음과 같다. : 0.1M KCl-0.01M 인산염 지지전해질, pH 7, 석출전위 0.00V, 그리고 석출시간 3분이었다. 이 조건에서 검출한계는 $3{\times}10^{-7}M$ (8ppb) $CN^-$이다.

• Archives of Pharmacal Research
• /
• 제24권2호
• /
• pp.100-104
• /
• 2001

Differential pulse polarographic(DPP) analytical procedure for the rifampicin antibiotic, which can be applied to monitor its synthetic process from the starting antibiotic of rifamycin B or rifamycin SV has been developed based on the electrochemical reduction of an azomethine group. Rifampicin exhibited a cathodic peak due to the azomethine group in the side chain of 3-[(4-methyl-1-piperazinyl)imino]methyl moiety and another cathodic peak due to the carbonyl group in rifamycin SV by DPP. The experimental peak potential shift of an azomethine reduction was -73 mV/pH in the pH range between 3.0 and 7.5, agreeing with involvement of 4 e-and 5 $H^5$ in its reduction. By the cyclic voltammetric(CV) studies, the azomethine and the carbonyl reductions in rifampicin were processed irreversibly on the mercury electrode. The plot of peak currents vs. concentrations of rifampicin ranging $1.0{\times}10^{-7} M~$1.0{\times}10^{-5} M yielded a straight line with a correlation coefficient of 0.9996. The detection limit was $1.0{\times}10^{-8} M with a modulation amplitude of 50 mV DPP has been successfully applied for the determination of rifampicin in the pharmaceutical preparations.