• Bulletin of the Korean Chemical Society
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• v.20 no.6
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• pp.696-700
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• 1999

A method has been developed for the determination of trace anion impurities in concentrated hydrogen peroxide. The method involves on-line decomposition of hydrogen peroxide, ion chromatographic separation and subsequent suppressed-type conductivity detection. H2O2 is decomposed in Pt-catalyst filled Gore-Tex membrane tubing and the resulting aqueous solution containing analytes is introduced to the injection valve of an ion chromatograph for periodic determinations. The oxygen gas evolving within the membrane tubing escapes freely through the membrane wall causing no problem in ion chromatographic analysis. Decomposition efficiency is above 99.99% at a flow rate of 0.4mL/min for a 30% hydrogen peroxide concentration. Analytes are quantitatively retained. The analysis results for several brands of commercial hydrogen peroxides are reported.

• Bulletin of the Korean Chemical Society
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• v.20 no.10
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• pp.1165-1171
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• 1999

The analysis of trace herbicides using the on-line SPE-HPLC system and a photochemical reaction was studied. 18 compounds of herbicides including eight triazines, six phenoxy acids and esters, and four other herbicides were examined. The on-line SPE-HPLC system developed for selection of eluting solvent improved chromatographic efficiency. The recoveries of herbicides were higher than 77%. With 100 mL tap water samples, the detection limits for all analytes were in the 0.1-2.3×10-10 M range. Detection was done by a UV or fluorescence spectrometer after photochemical reaction at the end of the column with 2W or 450W mercury lamp. Without a photochemical reaction, all compounds responded to 230 nm UV detector, but phenoxy acids and esters were weakly detected. However, with a photochemical reaction, these compounds were selectively detected at 320 nm wavelength of UV absorption and 400 nm emission of the fluorescence detectors. This method can be used for the analysis of environmental water containing herbicides at trace levels.

• ETRI Journal
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• v.44 no.3
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• pp.512-523
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• 2022

Random delay countermeasures introduce random delays into the execution flow to break the synchronization and increase the complexity of the side channel attack. A novel method for attacking devices with random delay countermeasures has been proposed by using a maximal overlap discrete wavelet transform (MODWT)-based power trace alignment algorithm. Firstly, the random delay in the power traces is sensitized using MODWT to the captured power traces. Secondly, it is detected using the proposed random delay detection algorithm. Thirdly, random delays are removed by circular shifting in the wavelet domain, and finally, the power analysis attack is successfully mounted in the wavelet domain. Experimental validation of the proposed method with the National Institute of Standards and Technology certified Advanced Encryption Standard-128 cryptographic algorithm and the SAKURA-G platform showed a 7.5× reduction in measurements to disclosure and a 3.14× improvement in maximum correlation value when compared with similar works in the literature.

• Current Optics and Photonics
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• v.7 no.4
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• pp.457-462
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• 2023

Quantitative measurement of trace ethane is important in environmental science and biomedical applications. For these applications, we typically require a few tens of part-per-trillion level measurement sensitivity. To measure trace-level ethane, we constructed a cavity ring-down spectroscopy setup in the 3.37 ㎛ mid-infrared wavelength range, which is applicable to multi-species chemical analysis. We demonstrated that the detection limit of ethane is approximately 300 parts per trillion, and the measured concentration is in agreement with the amounts of the injected sample. We expect that these results can be applied to the chemical analysis of ethane and applications such as breath test equipment.

• Analytical Science and Technology
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• v.20 no.3
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• pp.219-226
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• 2007

Glass is frequently encountered as types of materials that are submitted to forensic science laboratories as a result of trace evidence transfers. The repeatability and the reproducibility of trace element analysis were presented. An analysis of variance (ANOVA) was performed on laser ablation inductively coupled plasma spectrometric analyses of the fragments to identify the source. Pairwise comparisons were completed for all samples. In a pairwise comparison, each sample was compared to each other for a possible [n(n-1)/2] (n : numbers of the samples) total comparison to associate/discriminate samples using Tukey's HSD method. The aim of this study was to determine the utility of LA-ICP-MS for multi-element analysis of forensic samples. The 12 glass fragments from two manufacturers were collected and analyzed to identify the source. An analysis of variance (ANOVA) was performed on 31 elements in NIST 612 Trace elements in Glass. Elements were classified into four categories defined by the combination of precision and variation of inter-samples. We selected 11 elements, 209Bi, 90Zr, 121Sb, 178Hf, 59Co, 238U, 208Pb, 140Ce, 118Sn, 49Ti and 137Ba. 6 pairs out of 66 possible pairs were not distinguished when compared by 137Ba (p<0.05). However, all samples were distinguished using both 49Ti and 137Ba (p<0.05). In conclusion, multi-elemental analysis with LA-ICP-MS is a potential tecnique for the discrimination of forensic samples.

• Proceedings of the Korea Air Pollution Research Association Conference
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• 2004.05a
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• pp.139-140
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• 2004

• Proceedings of the Korea Technical Association of the Pulp and Paper Industry Conference
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• 2008.05a
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• pp.157-168
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• 2008

• Proceedings of the Korea Air Pollution Research Association Conference
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• 1999.04a
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• pp.298-299
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• 1999

• Proceedings of the Korean Society of Precision Engineering Conference
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• 2013.05a
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• pp.337-338
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• 2013

• Journal of the Korean Chemical Society
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• v.37 no.5
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• pp.477-482
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• 1993

The determination of trace level mercury in bio-materials has been investigated by the square wave anodic stripping voltammetry (ASV)-technique at glassy carbon electrode. Prior to analysis, the bio-materials were digested with HNO3/H2SO4 mixture and KMnO4 was added to complete the oxidation. The detection limit of the mercury varied greatly with deposition time, deposition potential, pH and stirring rate. When deposition is carried out for 240 sec with 400 rpm stirring at -1.0 volts vs. Ag/AgCl, the detection limit was below $0.5\;ppb\;(2.5{\times}10^{-9} M)$. The method is recommended for trace level mercury analysis of biomaterials because this procedure is time saving and has higher sensitivity.