• 전기화학회지
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• 제23권3호
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• pp.66-72
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• 2020

본 연구에서는 글루코스 검출을 위한 HRP (horseradish peroxidase)와 GOD (glucose oxidase)를 혼합한 형태의 다중 효소 반응 바이오센서 개발연구를 수행하였다. 바이오센서는 제작 시간 단축을 위하여 전기전착법을 이용하여 제작하였으며, 경제적인 센서 제작을 위하여 SPE (screen printed electrode)를 사용하였다. 다중 효소 바이오센서의 효과를 확인하기 위하여 단일 효소 바이오센서를 제작하여 비교 및 분석하였다. 센서의 특성을 평가하기 위해서 주사전자현미경(scanning electron microscopy, SEM), 순환전위법(cyclic voltammetry, CV), 전기화학적 임피던스 분광법(electrochemical impedance spectroscopy, EIS), 시간대전류법(chronoamperometry, CA), 흐름 주입분석법(flow injection analysis, FIA)를 수행하였다. SEM, CV, EIS의 분석결과로부터 효소가 전극 표면에 고정화가 잘 된 것을 확인하였고, CA로부터 제작된 다중 효소 바이오센서가 단일 효소 바이오센서에 비해 신호성능이 200% 향상된 것을 확인하였다. 이로부터 HRP와 GOD가 서로 촉매적으로 반응한다는 것을 설명할 수 있었다. 또한, FIA의 결과에서 동일한 농도의 글루코스 용액을 4회 나누어 주입하였을 때, 전류신호량이 일정함을 확인하였고, 농도에 따른 전류신호량을 분석하여 신호민감성, 재현성, 안정성 등이 우수함을 설명할 수 있었다.

• Bulletin of the Korean Chemical Society
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• 제18권3호
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• pp.316-318
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• 1997

A general and universal detection method, which can be used in high performance liquid chromatography (HPLC) and flow injection analysis (FIA) system for the determination of any metal ions complexing with ethylenediaminetetraacetic acid (EDTA), is demonstrated. Pulsed amperometric detection scheme is applied in a flow-through thin layer electrochemical cell at an Au working electrode. Fluctuation of peak current level at the same flow rate of carrier solution is minimized at this solid working electrode, whereas not at a dropping mercury electrode. Removal of dissolved oxygen can be omitted with this detection method, which is a required step for cathodic detection methods. Also, a group of metal ions can be determined selectively and indirectly with this detection scheme.

• 전기화학회지
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• 제13권4호
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• pp.251-255
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• 2010

We report on the electrocatalytic reduction of hydrogen peroxide at nanoporous gold (NPG) surfaces. Various NPG surfaces with different surface structure were prepared by changing the conditions of electrodeposition for Ag-Au layers such as the concentration ratios of $KAu(CN)_2$ over $KAg(CN)_2$ and deposition charges. The effects of different electrochemical conditions on the electrocatalysis of $H_2O_2$ reduction were investigated. The NPG surfaces exhibited sensitive amperometric responses for $H_2O_2$ reduction, from which calibration plots with higher sensitivity than a bare Au surface were obtained.

• Journal of Electrochemical Science and Technology
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• 제5권1호
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• pp.23-31
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• 2014

The DL-norvaline was electrochemically oxidized and deposited on the glassy carbon electrode surface using cyclic voltammetry (CV). The modified electrode was examined for electrochemical oxidation of hydroquinone (HQ) and catechol (CC). It exhibited good electrocatalytic ability towards their oxidation and simultaneous determination in a binary mixture using differential pulse voltammetry (DPV). The peak currents were linear to the concentration of HQ and CC, in the range from $5{\mu}M$ to $100{\mu}M$, and $4{\mu}M$ to $140{\mu}M$, respectively. The determination limits(S/N = 3) for HQ and CC were $1{\mu}M$ and $0.8{\mu}M$, respectively. The obtained modified electrode was applied to simultaneous detection of HQ and CC in water sample.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 1998년도 춘계학술대회 논문집
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• pp.423-426
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• 1998

Piezoresistive pressure sensors have fabricated using electrochemical etch-stop technique. Si diaphragm having thickness of n-epi. layer was fabricated and used to detect pressure range from 0 to 1 kg/$\textrm{cm}^2$. Piezoresistors were diffused 3${\times}$10$\^$18/ cm$\^$-3/ and placed at diaphragm edge for maximum pressure detection. The characteristics of electrochemical etch-stop in TMAH/lPA/pyrazine solution were also discussed. I-V curves of n and p-type Si in TMAH/lPA/pyrazine solution were obtained. Etching rate is highest at optimum etching condition, TMAH 25wt.%/IPA 17vo1.%/pyrazine 0.1/100m1, thus the elapsed time of etch-stop was reduced.

• 분석과학
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• 제17권6호
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• pp.464-469
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• 2004

순환 전압전류법을 이용하여, 1 mM 인산염 완충용액에서 루테늄-쿠페론 착물의 전기화학적 행동을 살펴보았다. 루테늄 정량의 최적 조건은 1 mM 인산염 완충용액 (pH 6.0), 0.1 mM 쿠페론의 용액에서 주사속도는 100 mV/s 이었다. 이 조건에서 농도 변화에 따른 선형 주사 전압곡선의 환원 봉우리 전류변화를 이용하여 얻은 루테늄의 검출 한계 ($3{\sigma}$)는 $1.2{\times}10^{-7}M$ 이다.

• 대한화학회지
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• 제37권4호
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• pp.453-461
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• 1993

테프론 코일과 저압 수은 램프를 사용, 간단하게 제작된 광화학 반응기를 이용한 HPLC 검출 방법을 연구하였다. 4종의 티오카바메이트 시료들을검출함에 있어 UV, 형광 및 전기화학 검출기 등에서 광화학 반응을 통한 액체 크로마토그래피 후컬럼 검출법의 유용성을 알아보았다. 액체 크로마토그래피를 통해 분리된 티오카바메이트류에 254nm의 UV을 조사할 경우 4종의 시료는 모두 광반응이 일어나 형광을 통해 분리된 티오카바메이트류에 254nm의 UV을 조사할 경우 4종의 시료는 모두 광반응이 일어나 형광을 나타내거나, 전기화학 검출기에 큰 검출 응답을 나타내었다. UV 검출법의 경우 광반응 생성물은 광반응전보다 검출감도는 감소하였으나 장파장쪽에서 검출이 용이하였다. 형광 검출법의 경우 광반응전 4종의 티오카바메이트는 전혀 검출되지 않았으나, 광반응 후 MPTC,CPTC는 Ph 4.0, 50% 아세토니트릴 이동상 조건에서 5.0~9.3ng의 검출한계를 나타내었다. 전기화학 검출법에서는 광반응전 시료가 매우 작은 검출 응답을 보였고, 광반응 후 시료는 5~20배 이상의 검출감도가 증대되었으며 13.3~0.02ng의 검출한계를 나타내었다. 이때 최적 검출조건은 50% 아세토니트릴 $-0.5{\times}10^{-2}$ M 인산 완충용액, pH 7.0 이었다. 또한 티오카바메이트의 광반응물과 OPA-MERC를 반응 코일내에 유도체를 형성시켜 형광검출기로 검출해냄으로써 광분해물에서 1차 아민이 생성됨을 알 수 있었다.

• 센서학회지
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• 제32권5호
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• pp.290-294
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• 2023

Among various types of harmful gases, hydrogen sulfide is a strong toxic gas that is mainly generated during spillage and wastewater treatment at industrial sites. Hydrogen sulfide can irritate the conjunctiva even at low concentrations of less than 10 ppm, cause coughing, paralysis of smell and respiratory failure at a concentration of 100 ppm, and coma and permanent brain loss at concentrations above 1000 ppm. Therefore, rapid detection of hydrogen sulfide among harmful gases is extremely important for our safety, health, and comfortable living environment. Most hydrogen sulfide gas sensors that have been reported are electrical resistive metal oxide-based semiconductor gas sensors that are easy to manufacture and mass-produce and have the advantage of high sensitivity; however, they have low gas selectivity. In contrast, the electrochemical sensor measures the concentration of hydrogen sulfide using an electrochemical reaction between hydrogen sulfide, an electrode, and an electrolyte. Electrochemical sensors have various advantages, including sensitivity, selectivity, fast response time, and the ability to measure room temperature. However, most electrochemical hydrogen sulfide gas sensors depend on imports. Although domestic technologies and products exist, more research is required on their long-term stability and reliability. Therefore, this study includes the processes from electrode material synthesis to sensor fabrication and characteristic evaluation, and introduces the sensor structure design and material selection to improve the sensitivity and selectivity of the sensor. A sensor case was fabricated using a 3D printer, and an Ag reference electrode, and a Pt counter electrode were deposited and applied to a Polytetrafluoroethylene (PTFE) filter using PVD. The working electrode was also deposited on a PTFE filter using vacuum filtration, and an electrochemical hydrogen sulfide gas sensor capable of measuring concentrations as low as 0.6 ppm was developed.

• Journal of Biosystems Engineering
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• 제41권2호
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• pp.138-144
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• 2016

Purpose: Phosphorus is an essential element for water quality control. Excessive amounts of phosphorus causes algal bloom in water, which leads to eutrophication and a decline in water quality. It is necessary to maintain the optimum amount of phosphorus present. During the last decades, various studies have been conducted to determine phosphorus content in water. In this study, we present a comprehensive overview of colorimetric, electrochemical, fluorescence, microfluidic, and remote sensing technologies for the measurement of phosphorus in water, along with their working principles and limitations. Results: The colorimetric techniques determine the concentration of phosphorus through the use of color-generating reagents. This is specific to a single chemical species and inexpensive to use. The electrochemical techniques operate by using a reaction of the analyte of interest to generate an electrical signal that is proportional to the sample analyte concentration. They show a good linear output, good repeatability, and a high detection capacity. The fluorescence technique is a kind of spectroscopic analysis method. The particles in the sample are excited by irradiation at a specific wavelength, emitting radiation of a different wavelength. It is possible to use this for quantitative and qualitative analysis of the target analyte. The microfluidic techniques incorporate several features to control chemical reactions in a micro device of low sample volume and reagent consumption. They are cheap and rapid methods for the detection of phosphorus in water. The remote sensing technique analyzes the sample for the target analyte using an optical technique, but without direct contact. It can cover a wider area than the other techniques mentioned in this review. Conclusion: It is concluded that the sensing technologies reviewed in this study are promising for rapid detection of phosphorus in water. The measurement range and sensitivity of the sensors have been greatly improved recently.

• Nano
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• 제13권11호
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• pp.1850134.1-1850134.10
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• 2018

Increasing active sites and enhancing electric conductivity are critical factors to improve sensing performance toward phenol. Herein, Ni nanoparticle was successfully anchored on acidified multiwalled carbon nanotube (a-MWCNT) surface by electroless plating technique to avoid Ni nanoparticle agglomeration and guarantee high conductivity. The crystal structure, phase composition and surface morphology were characterized by XRD, SEM and TEM measurement. The as-prepared Ni/a-MWCNT nanohybrid was immobilized onto glassy carbon electrode (GCE) surface for constructing phenol sensor. The phenol sensing performance indicated that Ni/a-MWCNT/GCE exhibited an amazing detection performance with rapid response time of 4 s, a relatively wide detection range from 0.01 mM to 0.48 mM, a detection limit of $7.07{\mu}M$ and high sensitivity of $566.2{\mu}A\;mM^{-1}\;cm^{-2}$. The superior selectivity, reproducibility, stability and applicability in real sample of Ni/a-MWCNT/GCE endowed it with potential application in discharged wastewater.