• Tribology and Lubricants
• /
• 제35권3호
• /
• pp.151-157
• /
• 2019

Insulated oil degradation produces charged by-products, such as acids and hydro-peroxides, which tend to reduce the insulating properties of the oil. In this study, UV-vis spectroscopy measurement technology is developed and experimentally compared with other measurement methods, such as the titration method and IR spectroscopy, to validate its ability to monitor the degradation of electrical insulating paper. The degradation characteristics of the insulating paper are appropriately represented through various types of measurement methods, such as the Tan (delta) method, $CO_2$ gas production measurement, the titration method, and IR spectroscopy. The results are demonstrated to be well comparable to a change in the fluorescence emission ratio (FER), which is defined as the shift in fluorescence intensity in the measured wavelength range, and also to the chromatic ratio, which is defined as a color shift to longer wavelength ranges. The results also show that, by using UV-vis spectroscopy, it is possible to detect the degradation of the insulating paper. This study suggests that UV-vis spectroscopy can be applied as an alternative to high-performance liquid chromatography, which is the internationally recognized measurement technology for cellulose paper degradation. The FER detector is also verified to be useful as an effective condition-monitoring device for power transformers.

• 한국작물학회지
• /
• 제48권5호
• /
• pp.369-371
• /
• 2003

Cyanidin 3-glucoside (C3G) content contained in the grains of blackish purple rice varieties, Heugjinjubyeo, Kilimheugmi, Heugnambyeo, Sanghaehy-anghyeolla, and the progenies derived from their crosses was evaluated by HPLC and UV-Vis spectroscopy. C3G content was higher in the range of 10-30% by using UV-Vis method compared to HPLC method. A significant linear relationship was, however, observed between two analytical methods. The correlation coefficient was 0.98. Thus, this results suggested that it would be able to use UV-Vis spectroscopy to determine C3G content which does not demanded precise value like selection.

• 분석과학
• /
• 제28권2호
• /
• pp.112-116
• /
• 2015

Extraction of quaternary ammonium compounds (choline and betaine) from plant samples (spinach) using ion exchange resin (AG1, OH⁻ form) is a very simple and inexpensive approach. However, it is very hard to determine amounts of choline and betaine simultaneously using high-performance liquid chromatography-ultraviolet (HPLC-UV) detection. Unlike choline, betaine has low molar absorptivity in UV-visible (UV-Vis) region, which makes it difficult to carry out UV-Vis detection of betaine. The mixture of quaternary ammonium compounds (choline and betaine) was derivatized using 2-bromo acetophenone as a derivatizing agent. As a result, choline did not react with the derivatizing agent, whereas betaine formed a betaine derivative. This betaine derivative exhibited detectable UV absorption with baseline separation between choline and the betaine derivative. Thus, with this method, choline and betaine can be determined simultaneously by using the HPLCUV method through one-step derivatization, which is an easy, sensitive, and reliable method.

• Bulletin of the Korean Chemical Society
• /
• 제32권5호
• /
• pp.1657-1661
• /
• 2011

In this study, CdSe-$TiO_2$ photocatalyst were synthesized by a facile solvothermal method and characterized by X-ray diffraction (XRD), Scanning electron microscopy (SEM) with energy dispersive X-ray (EDX) analysis and UV-vis diffuse reflectance spectrophotometer. The photocatalytic activity was investigated by degrading methylene blue (MB) in aqueous solution under irradiation of UV light as well as visible light. The absorbance of degraded MB solution was determined by UV-vis spectrophotometer. The results revealed that the CdSe-$TiO_2$ photocatalyst exhibited much higher photocatalytic activity than $TiO_2$ both under irradiation of UV light as well as visible light.

• 펄프종이기술
• /
• 제30권3호
• /
• pp.29-37
• /
• 1998

In order to set up a proper AKD quantification method for studing AKD hydrolysis, a quantitative analysis method using Uv/vis spectroscopy was evaluated and compared to the conventional GC-MS analysis. Hydrolysis rates of AKD emulsions during storage at 4$0^{\circ}C$ were measured by the UV/vis analysis. Owing to its simplicity and capability of measuring the unreacted AKD significantly even in a small amount, UV/vis method proved to be more suitable for studing AKD hydrolysis than GC-MS analysis. AKD hydrolysis was affected by the types of emulsifiers. Polymer stabilized AKD emulsion hydrolyzed more rapidly than starch stabilized AKD.

• 분석과학
• /
• 제33권3호
• /
• pp.115-124
• /
• 2020

마킹펜류는 어린이제품법의 안전확인으로 관리되는 학용품 품목으로서, 폼알데하이드 함유량에 대한 안전기준은 20 mg/kg이다. 시중에 유통되는 마킹펜 9 종을 현행 시험법인 백포 필기 후 증류수 추출액을 UV/Vis 흡광광도계로 분석(이하 Nash-UV/Vis 방법)한 결과 폼알데하이드가 검출되지 않았고 수성 잉크와 같이 항시 추출액이 유색을 띠는 경우 거짓 양성 결과를 보였다. 반면, 잉크를 직접 초음파를 이용하여 용해한 증류수 액을 DNPH 유도체화 한 후 HPLC/DAD로 분석(이하 DNPH-HPLC/DAD 방법)한 결과, 최소 3.2 mg/kg ~ 최고 93.2 mg/kg이었고, 3 종 제품이 안전기준 20 mg/kg을 초과하였다. 따라서, 추출과정이 빠르고 용이하도록 잉크를 직접 증류수에 용해한 후 DNPH-HPLC/DAD 분석 방법으로 잉크 내 폼알데하이드 안전기준 20 mg/kg 이하 여부를 판단할 수 있도록 제안하고자 하며, 이 방법은 Nash-UV/Vis 방법의 검출한계 및 색상 물질 추출 시의 거짓 양성 결과의 한계를 극복할 수 있다. 형광펜, 보드마카, 물백묵, 페인트마카의 잉크 매트릭스를 사용하여 20 mg/kg 및 40 mg/kg의 범위에서 스파이킹 방법으로 산출한 DNPH-HPLC/DAD 분석방법의 정확도 및 정밀도는 각각 90.1 ~ 105.4 % 및 0.6 ~ 3.3 %이다.

• 약학회지
• /
• 제53권5호
• /
• pp.235-240
• /
• 2009

The interaction of cadmium (II) ion with quercetin was investigated in aqueous solution at different pH. The quercetin/cadmium stochiometries for cadmium (II) binding have been determined by UV-vis spectrophotometric method. The complexation of Cd(II) ion with 54.72 ${\mu}M$ quercetin (A=1.00793) was formed in 0.2 M $NH_3-0.2$ M $NH_4Cl$ (pH 8.0) buffer solution. 1:1 Cd(II)-complex had a maximum absorbance and showed the bathochromic shift of the long-wavelength band of the UV-vis spectra in the alkaline pH when interacted with quercetin in buffer solution. These results suggest that Cd(II)-quercetin complex has the optimal condition of chelation in basic buffer solution.

• 공업화학
• /
• 제27권6호
• /
• pp.669-671
• /
• 2016

본 연구에서는 수열합성법을 이용하여 수산화인회석을 합성하였다. 또한 이온 교환 반응을 통하여 수산화인회석 표면에 은을 도입하였다. 합성된 샘플의 결정성과 형태를 X-선 회절 분석과 투과전자현미경을 통하여 분석하였으며, 산란 반사 UV-vis 스펙트럼을 통하여 합성한 샘플의 광학적 특성을 조사하였다. 은이 도핑된 수산화인회석의 경우 은이 수산화인회석 표면에 나노입자 형태로 존재한다는 것을 X-선 회절 분석과 투과전자현미경 실험으로 확인하였다. 특히 수산화인회석과 비교하여 은 나노 입자가 도입된 수산화인회석의 경우에는 UV-Vis 영역에서 높은 흡광도를 나타내었다.

• Bulletin of the Korean Chemical Society
• /
• 제35권11호
• /
• pp.3275-3279
• /
• 2014

A mass balance method for purity assessment of thermolabile organic reference materials was established by combining several techniques, including liquid chromatography with UV/VIS detector (LC-UV), Karl-Fischer (K-F) Coulometry, and thermal gravimetric analysis (TGA). This method was applied to three fluoroquinolones like enrofloxacin, norfloxacin and ciprofloxacin. LC-UV was used to analyze structurally related organic impurities based on UV/VIS absorbance spectra obtained in combination with LC separation. For all three organic reference materials, the UV/VIS spectra of the separated impurities were similar to that of the major component of the corresponding materials. This indicates that the impurities are structurally related to the respective reference material sharing common chromophores. Impurities could be quantified by comparing their absorbances at the wavelength of maximum absorbance (${\lambda}_{max}$). The water contents of the reference materials were measured by K-F Coulometry by an oven-drying method. The total inorganic impurities contents were assayed from ash residues in TGA analysis with using air as a reagent gas. The final purities estimated from results of those analytical techniques were assigned as ($99.91{\pm}0.06$), ($97.09{\pm}0.17$) and ($91.85{\pm}0.17$)% (kg/kg) for enrofloxacin, norfloxacin and ciprofloxacin, respectively. The assigned final purities would be applied to the reference materials which will be used as calibrators for the certification of those compounds in matrix CRMs as starting points for the traceability of their certified values to SI units.

• 분석과학
• /
• 제18권5호
• /
• pp.425-430
• /
• 2005

본 연구에서는 대기 중 암모니아 성분의 농도 계측에 활용하는 간이비색계의 성능을 UV/VIS 분광계에 대비하는 방식으로 평가하였다. 본 연구의 목적상 두 가지 분석 시스템을 이용하여 검출한계, 재현성, 직선성, 정확도 등의 기준항목을 다양하게 비교하였다. 본 연구에 의하면, 간이비색계의 성능은 대체로 UV/VIS 분광계와 양호한 일치도를 보일 정도로 좋은 결과를 보였다. 검출한계를 평가한 결과 두 가지 시스템 모두 $3{\mu}g$에 가깝게 나타났다. 그러나 간이비색계의 경우, 아주 낮은 농도와 고농도대에서 상대적으로 문제점이 존재하는 것으로 나타났다. 예를 들어, 암모니아의 절대량이 $10{\mu}g$ 이하일 때는 재현성에 대한 문제가 두드러졌고, $100{\mu}g$ 이상의 고농도대에서는 직선성이 제한되는 문제로 인해 분석이 어려웠다. 따라서 만약 대기시료를 30 리터 정도로 채취한다고 가정하면, (별다른 희석을 가하지 않고 분석한다면) 500 ppb에서 5 ppm의 농도대에서 간이비색계를 적용하는 것이 유효한 것으로 나타났다. 농도대에 따른 간이비색계의 제한적인 특성을 충분히 감안하고 사용할 경우, 간이비색계를 활용한 분석은 상당히 양호한 결과를 생산하는 것이 가능하다는 결론을 내릴 수 있다.