• Preventive Nutrition and Food Science
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• 제3권1호
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• pp.36-42
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• 1998

Ion-selective eleltrodes(ISEs) are simple electrodechemical devices for the direct measurement of ions in the samples. A novel potentiometric biosensor for the determination of L-Malate or D-isocitrate has been developed by using CO2-3 -ISE-FIA system was composed of a pump, an injector, a malic enzyme or isocitric dehydrogenase enzyme reactor, a CO2-3 -ISE, a pH/mV meter, and an integrater. The various factors, such as buffer capacity types of plstericizer and polymer, were optimized for the CO2-3 selectivity. In this novel CO2-3 --ISE-FIA system, the potential difference due to the amount of CO2-3 produced from each enzyme reaction was proportional to the amount of L-malate or D-isocitrate.

• 약학회지
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• 제46권5호
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• pp.320-323
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• 2002

A method for the determination of acidic drug, mefenamic acid and ibuprofen with ion-selective electrode(ISE) using Fe(II)-di-2-pyridyl ketone oxime complex as a counter ion were developed. Benzyl-2-nitrophenyl ether(BNPE) plasticized membrane was more selective and sensitive than the other tested membranes. The acidic drug selective electrode exhibits a linear response for 10$^{-2}$ M 510$^{-5}$ M of acidic drugs, mefenamic acid and ibuprofen with a slope of -55.9 and -56.3 mV/dec. in borate buffer solution (pH 8.9). Potentiometric selectivity measurements revealed negligible interferences from aromatic and aliphatic carboxylic acid salts. The electrodes were found to be useful for the direct determination of mefenamic acid and ibuprofen in pharmaceutical preparations.

• 한국안전학회지
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• 제6권4호
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• pp.13-20
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• 1991

Ion-selective electrode responsive to the thiocynate ion prepared by using the quaternary ammonium salts as a active material and PVC as a membrane matrix. The effect of chemical structure and composition of active material, and the membrane thickness on the linear response. the detection limit, and Nernstian slope of the electrode studied. Under the above optimum conditions of membrane, the effect of pH and the selectivity coefficients to various interfering anions were compared and investigated. It was concluded that the functions of thiocynate ion-selective electrode(ISE) were closely related to the chemical structure of the quaternary ammonium salts. The linear response, and the detection limit of the electrode potential increased with the increase of the carbon chain length of the alkyl group in the quaternary ammonium salts in the ascending order of Aliquat 336T, TOAT, TDAT, and TDDAT. The optimum membrane thickness was 0.3mm. The electrode characteristics was better with the decrease of the concentration of active material, and the best concentration was 3 weight percent. The membrane potential was independent of the pH variation in the region from pH 2 to 12. The order of the selectivity coefficients is as follows：Cl $O_4$$^{[-10]}$ ＞ $I^{[-10]}$ ＞N $O_3$$^{[-10]}$ ＞B $r^{[-10]}$ ＞ $F^{[-10]}$ ＞C $l^{[-10]}$ ＞O $A_{c}$ $^{[-10]}$ 〓S $O_4$$^{2-}$.

• Journal of Biosystems Engineering
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• 제41권2호
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• pp.75-84
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• 2016

Purpose: In-situ water quality monitoring based on ion-selective electrodes (ISEs) is a promising technique because ISEs can be used directly in the medium to be tested, have a compact size, and are inexpensive. However, signal drift can be a major concern with on-line management systems because continuous immersion of the ISEs in water causes electrode degradation, affecting the stability, repeatability, and selectivity over time. In this study, a computer-based nitrate monitoring system including automatic electrode rinsing and calibration was developed to measure the nitrate concentration in water samples in real-time. Methods: The capabilities of two different types of poly(vinyl chloride) membrane-based ISEs, an electrode with a liquid filling and a carbon paste-based solid state electrode, were used in the monitoring system and evaluated on their sensitivities, selectivities, and durabilities. A feasibility test for the continuous detection of nitrate ions in water using the developed system was conducted using water samples obtained from various water sources. Results: Both prepared ISEs were capable of detecting low concentrations of nitrate in solution, i.e., 0.7 mg/L $NO_3-N$. Furthermore, the electrodes have the same order of selectivity for nitrate: $NO_3{^-}{\gg}HCO_3{^-}$ > $Cl^-$ > $H_2PO_4{^-}$ > $SO{_4}^{2-}$, and maintain their sensitivity by > 40 mV/decade over a period of 90 days. Conclusions: The use of an automated ISE-based nitrate measurement system that includes automatic electrode rinsing and two-point normalization proved to be feasible in measuring $NO_3-N$ in water samples obtained from different water sources. A one-to-one relationship between the levels of $NO_3-N$ measured with the ISEs and standard analytical instruments was obtained.

• 한국작물학회:학술대회논문집
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• 한국작물학회 2022년도 추계학술대회
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• pp.153-153
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• 2022

There is a growing need to develop ion sensors for agriculture. As a result, several technologies have been developed, such as colorimetry, spectrophotometry, and ion-selective electrode (ISE). Among them, ISE has some advantages compared to others. First, it does not require pre-treatment processes and expensive equipment. Second, it is possible for the portable detection system by introducing small-sized electrodes. Finally, real-time and multiple detections of several ions are pursued. It is well-known that N, P, and K nutrients are critical for crop growth. With the development of agriculture techniques, the importance of soil nutrient analysis has attracted much attention for cost-effective and eco-friendly agriculture. Among several issues, minimizing the use of fertilizers is significant through quantitative analysis of soil nutrients. As a result, it is highly important to analyze certain nutrients, such as N (ammonium ion, nitrate ion, nitrite ion), P (dihydrogen phosphate ion, monohydrogen phosphate ion), and K (potassium ion). Therefore, developing sensors for accurate analysis of soil nutrients is highly desired. n this study, several ISEs have been fabricated to detect N, P, and K. Their performance has been intensively studied, such as sensitivity, selectivity coefficient, and concentration range, and compared with commercialized ISEs. In addition, preliminary tests on the in-situ N, P, and K monitoring have been conducted inside the soil.

• Journal of Biosystems Engineering
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• 제32권1호
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• pp.37-43
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• 2007

This study was carried out to investigate the applicability of PVC membrane-based ion-selective electrodes for macronutrients (K, Ca, and N) by measuring of potassium, calcium, nitrate ions in hydroponic nutrient solution. The capabilities of two ion-selective membranes with varying chemical compositions for each ion were evaluated in terms of sensitivity, selectivity, and lifetime to choose sensing elements suitable for measuring typical ranges of nutrient concentrations in hydroponic solutions. The selected calcium and nitrate ion-selective membranes showed effectively sensitive responses to calcium and nitrate ions with lifetimes of 25 and 15 days, respectively. The addition of a cation additive to the potassium membrane cocktail allowed its sensitivity to be increased whereas its lifetime was reduced from 30 days to 10 days.

• 대한화학회지
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• 제55권1호
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• pp.63-69
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• 2011

이 작업은 수송체로서 N,N'-bis(2-hydroxybenzyl)-1,3-diaminopropane (L1)과 N,N'-bis(2-hydroxybenzyl)-2,2-dimethyl-1,3-diaminopropane (L2)에 기초한 $Ag^+$ 이온-선택 전극의 제조, 개발 그리고 전압반응에 대해 토의한다. $Ag^+$에 대하여 L1에 기초한 전극은 58.7 mV/dec에 도달하는 안정한 Nernst에 가까운 기울기와 $1.0{\times}10^{-6}M$의 검출한계를 갖는 등급의 최소 다섯가지 순서의 선형범위에서 최적의 전압 반응 특징을 보이는 것을 나타낸다. 제안된 전극은 다른 테스트한 양이온과 비교하여 $Ag^+$에 우위의 선택성을 보였다. 훌륭한 전압 분석적 특징은 중요한 진짜 샘플에서 은의 순도분석의 성공적인 응용을 이끌 것이다. 그리고 그것은 제안된 $Ag^+$-ISE가 측정 능력의 중요한 진보를 보여준다는 것을 나타내고 있다. 그러나 L2에 기초한 전극에 대해서는, 약한 전압 반응 특징들이 전체 실험 과정에서 관측되었다.

• 전기화학회지
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• 제9권3호
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• pp.132-134
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• 2006

본 연구에서는 테트라싸이크린 항생제를 양이온선택성 전극의 담체로 사용한 막전극을 제작하고 알칼리 및 알칼리 토금속에 적용하여 전위차 감응도를 조사하였다. 제작된 전극은 지용성 첨가제의 유무와 관계없이 $Ca^{2+}$ 이온에 대해서 거의 이상적인 전위차 감응도를 나타내었다. 또한 $Mg^{2+}$를 제외한 다른 양이온에도 이상적인 네른스트값에 80% 이상의 감응도와 $10^{-5}$ 이하의 검출한계를 나타내었다. 수명, 감응시간, 재현성 등도 이온선택성 전극에 응용하기에 문제가 없었다.

• 한국축산식품학회지
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• 제28권3호
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• pp.301-305
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• 2008

조제분유중의 요오드 및 염소를 신속하고 정확하게 분석하기 위해 이온선택성 전극을 이용한 분석을 실시하였다. 전극을 이용한 측정시 영향을 주는 간섭물질을 제거하기 위해 시료를 용해한 후 3% 아세트산 2 mL를 투입하고, 정제는 filter paper(No.541, Whatman, UK)를 이용하여 여과하는 방법을 선택하였다. 요오드 및 염소이온이 pH에 의해 영향을 받는 것을 확인할 수 있었으며, 0.1 N NaOH를 사용하여 pH를 7.0으로 보정하여 농도를 측정함으로써 요오드와 염소의 회수율 각각 $93.7{\pm}2.7%$와 $103.9{\pm}4.9%$의 결과를 얻을 수 있었다. 간단하고 신속한 간섭물질 제거와 정제를 통해 조제분유중의 요오드 및 염소이온의 농도를 이온전극으로 신속하고 정확하게 측정할 수 있었다.

• 대한화학회지
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• 제48권3호
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• pp.266-272
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• 2004

소형 고체상 전극에 단일 조성 실온 경화형(one-component room temperature vulcanizing type) 실리콘러버 730(730 RTV)을 지지체로 도입하여 가소제가 필요 없는 탄산이온선택성 전극막을 개발하였다. 본 연구에서 최적화된 탄산이온선택성 전극막의 조성은 85.75 wt%의 730 RTV, 11.08 wt%의 trifluoroacetyl-p-decylbenzene(TFADB), 3.17 wt%의 tridodecyl-methylammonium chloride(TDMACl)로 제조 되었고, 우수한 전기화학적 특성(감응기울기 (26.3 mV/dec.), 선택성($logKT^{pot}_{CO_{2},Cl^-}$= -4.00, $logKT^{pot}_{TCO_{2},Sal^-}$=1.69), 검출한계(4.0${\times}10^{-4}M$))을 보였으며, 이와 같은 조성의 막을 도입한 평면형 고체상 센서는 60일 이상 초기특성을 유지하였다.