Antioxidants are food additives that extend the shelf life of food products by preventing lipid rancidity caused by active oxygen. They can either be naturally-derived or manufactured synthetically via chemical synthesis. In this study, method validation of five synthetic antioxidants, namely butylated hydroxyanisole, butylated hydroxytoluene, tertiary butylhydroquinone, propyl gallate, and disodium ethylenediaminetetraacetic acid, was performed using a high performance liquid chromatography–ultraviolet visible detector, and the method applicability was evaluated by analyzing foods containing antioxidants. The coefficient of determination (R2) average was 0.9997, while the limit of detection and limit of quantification were 0.02–0.53 and 0.07–1.61 mg/kg, respectively. The intra and inter-day accuracies and precisions were 83.2±0.7%–98.7±2.1% and 0.1%–5.7% RSD, respectively. Inter-laboratory validation for accuracy and precision was conducted using the Food Analysis Performance Assessment Scheme quality control material. The results satisfied the guidelines presented by the AOAC International. In addition, the expanded uncertainty was less than 16%, as recommended by CODEX. Consequently, to enhance public health safety, the results of this study can be used as basis data for evaluating the intake of synthetic antioxidants and assessing their risks in Korea.

Complexing agents used at various nuclear facilities exist in low- and intermediate level radioactive wastes deposited in the repository site. In addition these will be generated through the degradation of the wastes such as cellulose materials. The presence of chelating agents may possibly affect the safety of the wastes repository by promoting the migration of radionuclides into geosphere. Thus, under Nuclear Safety and Security Commission’s Notice No. 2021-16, the contents of chelating agents in radioactive wastes are required to be determined for the secured disposal. UV-Vis method based on an enzymatic reaction was proved to be in adequate to analyze citric acid in radioactive wastes with complex matrix, especially for concrete. A rapid automated method using ion chromatography (IC) for analysis of citric aicd in concrete samples is developed. This automated method enables a sample solution to measure without pretreatment and a target substance to separate from other concrete admixtures. Also, the developed method here, for radioactive concrete wastes was successfully applied to real samples with lowering a limit of quantification value.

Alfalfa is one of the most useful forage crops worldwide, containing a high level of amino acids that are essential to both human and animal health. However, amino acids and their concentrations may differ between plant parts. Hence, detecting amino acids in different plant parts would be useful in the development of diet supplements. The purpose of this study was to determine the amino acid content in alfalfa leaves, stems, and inflorescences using an amino acid analyzer. Asparagine and glutamic acid were the most abundant amino acids found in stems, leaves, and inflorescences than other amino acids. All parts of alfalfa had low concentrations of cysteine and methionine. All amino acids except asparagine were present in the highest concentration in leaves followed by inflorescences. Leaf had a rich amino acid content, namely asparagine, glutamic acid, leucine, proline, and lysine. However, the stem had a lower amino acid composition than the leaf or inflorescence. Overall, the data showed determining the amino acid content of forages provides a good approach to making animal feed with essential and specific amino acids and preventing excessive inclusion of amino acids.

The central theme of this work is the synthesis of single-walled carbon nanotubes (SWCNTs) through the chemical vapor deposition method (CVD). Single-walled carbon nanotubes are synthesized using catalyst-chemical vapor deposition of acetylene at 750 °C temperature. X-ray diffraction study gives a characteristic peak (002) at 26.55° corresponding to the existence of carbon nanotube confirms that the particles are crystalline in nature and hexagonal phase. An SEM and HRTEM outcome gives surface morphology of SWCNTs. The elemental composition was confirmed by EDAX. The ideal concentration of single-walled carbon nanotubes was used to design a novel electrochemical sensor for determining paracetamol (PA) using cyclic voltammetry. Electrochemical determination of paracetamol is described using a single-walled carbon nanotube modified carbon paste electrode (SWCNT/MCPE). The SWCNT/MCPE was used in this study to detect paracetamol electrochemically at pH 7.2 in a 0.2 M PBS with a scan rate of 50 mV s− 1. A single-walled nanotube modified carbon paste electrode was used to develop a sensitive and selective electrochemical technique for the detection of PA. The SWCNT/MCPE showed excellent electrocatalytic activity towards the oxidation of paracetamol in phosphate buffer solution. Therefore, with increased oxidation currents, the voltammetric responses of paracetamol at the bare carbon paste electrode are organized within cyclic voltammetric peaks.

계란의 비린내 강도는 가금류의 종류와 개인의 인식에 따라 다르지만 여러 요인에 의해 발생할 수 있다. 특히 트 리메틸아민(TMA)이 원인으로 밝혀졌다. 주목할만한 점은 리보플라빈이 TMA를 무취의 트리메틸아민-N-옥사이드로 전환시키는 역할을 하는 효소인 플라빈 함유 모노옥시게 나제 3의 활성을 증가시킬 수 있다는 점이다. 본 연구는 난황의 TMA 함량을 분석하여 비린내에 대한 기여도를 평 가하고, 비린내를 방지하는 방법을 개발하는 것을 목적으 로 하였다. 고체상 미세추출-기체 크로마토그래피/질량 분 석법을 사용하여 리보플라빈이 강화, 보충된 사료를 먹인 암탉의 난황에 있는 휘발성 화합물을 감지하고 정량화했다. 또한 샘플 간 휘발성 물질의 상대적 함량을 비교하기 위해 전자코를 이용하여 상관관계 연구를 수행하였다. TMA는 콜린이 함유된사료를 섭취한 가금류의 난황에서 고농도로 검출되었지만 리보플라빈이 보충된 사료를 섭취한 가금류 에서는 검출되지 않았다. 전반적으로, 이 연구는 리보플라 빈이 TMA를 포함하여 계란에 존재하는 휘발성 물질의 양 과 품질에 영향을 미친다는 것을 시사한다. 이러한 발견 이 계란의 비린내를 줄이는 것은 물론 품질 향상에 기여 하기를 기대한다.

Radioactive wastes that are generated as a result of operating NPPs, contain 63Ni and 59Ni that should be analyzed in accordance with the notice of Nuclear Safety and Security Commission (NSSC) for the acceptance of Korea Radioactive Waste Agency (KORAD). Analyzing 63Ni and 59Ni has few challenges to determine activities of each nuclide in radioactive waste sample that contains both nuclides. As is well known, 63Ni can be analyzed by liquid scintillation counter (LSC) detecting its emitted beta rays, however, beta rays emitted from 59Ni are overlapped on the spectrum. Therefore, to discriminate those two nuclides, spectrum channel should be divided according to its dedicating part of the spectrum. For instance, 59Ni contribute to spectrum channel 30–250, on the other hand, 63Ni contributes to spectrum channel 30–450. In other word, 63Ni solely can be analyzed on the channel from 260 to 450. To analyze both 63Ni and 59Ni using this channel division method, detection efficiency must be measured in advance; efficiency of 63Ni and 59Ni at ch. 30–250, and efficiency of 63Ni at ch. 260–450, then the activity can be calculated using the corresponding efficiency. In this study, for verifying the feasibility of channel division method, 5 simulated samples were prepared with different ratio of 63Ni/59Ni. The ratio varies as 1, 2, 10, 20 and 100 spiking standard source of 63Ni and 59Ni. Each sample was mixed with scintillation cocktail and detected for 90 minutes by LSC (300SL, Hidex) after the stabilization of solutions. As a result, calculated 63Ni activities for all sample were averaged as 97% of spiked activity. However, calculated 59Ni activity were 101%, 103%, 128%, 140%, 260%, respectively. The result indicates that 59Ni cannot be discriminated by channel division method when it exists in the sample with high 63Ni over 10 times then 59Ni such as radioactive waste sample. However, the results also show that the channel division method for analyzing 63Ni activity was successful verifying it can determine the activity of 63Ni regardless of the affect of 59Ni on the spectrum.

Chelating agents, such as EDTA, NTA, and citric acid, can form radionuclide-chelate complexes that may enhance the migration of radionuclides from disposal sites. Therefore, the contents of these chelators in radioactive wastes are determined for the secured disposal. In this study, a rapid automated method using ion chromatography (IC) is described for analysis of chelating agents. The method enables direct use of a sample solution for the measurement unlike colorimetric or enzymatic methods. In these cases, lots of chemicals are consumed to convert the chelating agents to be UV-Vis-active compounds during the pretreatment process and finally, absorbance or transmittance are measured at specific wavelength using UV-Vis spectrophotometer. In particular, the enzymatic method for determination of citric acid, because of its strong dependence on experimental conditions including sample types and chemical reagents may produce inconsistent results. The automated system using IC allows a laboratory to directly measure the amount of citric acid while reducing total analysis time and increasing efficiency. In addition, this method is capable of detecting a trace amount of citric acid, thereby lowering LOD and LOQ values.

Technetium-99 (99Tc) is a challenging radionuclide from presents many problems related to safe disposal. The measurement of 99Tc is of particular interest due to its high mobility, and the fact that it is a beta-emitter with a long half-life (t1/2=2.13×105 years) with long-term radiological effects[1]. As an isotopes of 99Tc, 99mTc has been widely applied for medical diagnosis and medical research. It is reported that the 99mTc has been used in 80% of diagnostic nuclear medicine procedures and almost 30 million examinations are conducted worldwide using this isotope. Because 99mTc has a short half-life of 6 h and decays to 99Tc, monitoring and safe disposal of 99Tc from human urine is very important, and concern is increasing every day as global use of 99mTc has increased by more than 4.5×1014 Bq per week and is increasing continuously[2]. However, the current methods for the detection of this radionuclide in such mdium are time consuming and can not satisfy for the low level urine sample analysis. In this work, a method for rapid determination of 99Tc in urine samples was developed. The sample was firstly pre-treated with K2S2O8 to decompose the organic matters combined with 99Tc in 0.5 mol·L−1 HNO3 medium at 100°C. Then the sample solution was loaded to a TEVA column (2 mL) for 99Tc separation and purification. The target element was finally measured by high resolution inductively coupled plasma mass spectrometry (HR-ICPMS). The developed analytical method was proved to be reliable and can be used to rapid determine low-level 99Tc in urine samples.

Radioactivity of radiostrontiums, Sr-89 and Sr-90, which are both pure beta-emitters, are generally measured via Cherenkov counting. However, the determination of Cherenkov counting efficiencies of radiostrontiums requires a complicated procedure due to the presence of Y-90 (also a pure betaemitter) which is the daughter nuclide of Sr-90. In this study, we have developed a machine learning approach using a linear regression model which allows an easier and simultaneous determination of the Cherenkov counting efficiencies of the radiostrontiums. The linear regression model was employed because total net Cherenkov count (Ct) from the three beta-emitters at time t after the separation of Y- 90, can be expressed as a linear combination of their respective time-varying radioactivities with their respective coefficients (parameters) being their counting efficiencies: Ct = εSr-90[ASr-90·exp(–λSr-90·t)] + εSr-89[ASr-89·exp(–λSr-89·t)] + εY-90[ASr-90·exp(1–λSr-90·t)], where ε is a counting efficiency, A is an initial activity, λ is a decay constant and t is time after the separation of Y-90, Thus, if we train the model with multiple Cherenkov counts measured from the three beta emitters, then we can obtain their estimates for counting efficiencies (so-called parameters) straightforward. For this, the model has been trained by two methods: Ordinary Least Squares (OLS) and Bayesian linear regression (BLR), for which two software packages, PyMC3 and Stan were employed to compare their performances. The results showed that the accuracy of the OLS was worse than that of the BLR. Particularly, the counting efficiency of Sr-90 was estimated to be smaller than 0, which is an unrealistic value. On the other hand, the estimates of the BLR gave realistic values which are close to the true values. Additionally, the BLR was able to provide a distribution for each counting efficiency (so-called “posterior”) from which various types of inference can be made including median and credible interval in the Bayesian statistics which is analogous to, but different from confidence interval in the Frequentist statistics. In the results of the BLR, the Stan package gave more accurate estimates than the PyMC3 package. Therefore, it is expected that counting efficiencies of the radiostrontiums including radioyttrium can be determined at the same time, more easily and accurately, by using the BLR with the Stan package and that the activities of radiostrontium also can be determined more easily by using the BLR if we know their counting efficiencies in advance. It is worth noting that the usage of the linear regression model in this study was different from the usual one where the trained model is used to predict a response value (count) from a set of unseen regressor values (activities).

210Po is a naturally occurring radionuclide of 238U decay series with a half-life of 138.4 days. 210Po is decay products of 222Rn, which escapes into the atmosphere and present in all environments with aerosol particles. Also, 210Po has high radiotoxicity and emits a high alpha energy of 5.305 MeV, and it decays to finally become a stable isotope, 206Pb. Therefore, 210Po entering the body by continuously ingestion or inhalation is likely to cause severe damage to the bone marrow, kidney and spleen and other sites in the body. Accordingly, the World Health Organization (WHO) recommends that screening level of gross alpha for drinking water not exceed 0.5 Bq·L−1. Alpha spectrometry has been mainly used for analysis of 210Po, and for the accurate measurement of alpha particle with short range, it is essential to prepare suitable source for alpha detection. The 210Po alpha source is made by a spontaneous deposition method in which polonium is adsorbed thin and flat onto a metal disc, such as silver, nickel and copper. There are various pretreatment methods to separate and concentrate polonium from water samples prior to spontaneous deposition, including Fe(OH)3 or MnO2 co-precipitation and evaporation. However, in the case of co-precipitation, sample contamination or loss of polonium may occur through the experimental processes, and evaporation lead to not only time-consuming process but also may cause loss of polonium due to the low boiling point of polonium. Therefore, in order to compensate for these problems, an efficient polonium analysis method that directly collects polonium from the original sample without a pretreatment is required. In this study, 210Po in bottled drinking water sold in Korea was analyzed using alpha spectrometry. A high purity silver disc (99.99%) was inserted into a newly designed polonium deposition kit to quickly and conveniently collect polonium from a water sample. The polonium alpha detecting source was made effectively only by the spontaneous deposition method without a complicated pretreatment. The source was measured using a PIPS detector, and the radioactivity concentration of 210Po was calculated using 209Po as a yield tracer.

농업기계는 다양한 환경과 작물을 대상으로 작업을 수행하기 때문에 농업기계의 설계와 개발은 실 작업 부하를 고려하여 수행되어야 한다. 따라서 본 연구에서는 식용 옥수수 수확기의 실 작업 부하를 계측하기 위해 식용 옥수수 수확 시험을 수행하였다. 또한, 계측된 부하 데이터를 이용하여 수확기 내 기어박스 요소들의 강도 및 수명을 평가하기 위한 부하 스펙트럼을 구축하였다. 부하 스펙트럼은 기어박스의 구성요소 중 기어와 베어링에 적용 가능한 하중 지속 분포와 기어와 베어링을 제외한 축, 하우징, 캐리어 등에 적용 가능한 부하 스펙트럼으로 나누어 구축하였다. 본 연구를 통해 구축된 하중 지속 분포 및 부하 스펙트럼은 식용 옥수수 수확기의 기어박스 강도 및 수명 평가뿐만 아니라, 기어박스의 설계 하중으로도 활용이 가능할 것으로 보인다.

Bullets flying with a light from the back are called “tracers”. Tracers are ignited by the combustion gas of the propellant and emit bright light that allows the shooter to visually trace the flight path. Therefore, tracers mark the firing point for allies to assist shooters to hit target quickly and accurately. Conventional tracers are constructed with a mixture of an oxidizing agent, raw metal, and organic fuel. Upon ignition, the inside of the gun can be easily contaminated by the by-products, which can lead to firearm failure during long-term shooting. Moreover, there is a fire risk such as forest fires due to residual flames at impact site. Therefore, it is necessary to develop non-combustion type luminous material; however, this material must still use the heat generated from the propellant, so-called “thermoluminescence (TL)”. This study aims to compare the TL emission of Dy3+, La3+ and Ho3+ doped MgB4O7 phosphors prepared by solid state reaction. The crystal structures of samples were determined by X-ray diffraction and matched with the standard pattern of MgB4O7. Luminescence of various doses (200 ~ 15,000 Gy) of gamma irradiated Dy3+, La3+ and Ho3+ (at different concentrations of 5, 10, 15 and 20 %) doped MgB4O7 were recorded using a luminance/color meter. The intensity of TL yellowish (CIE x = 0.401 ~ 0.486, y = 0.410 ~ 0.488) emission became stronger as the temperature increased and the total gamma-ray dose increased.

This work describes the facile synthesis of silver nanoparticle-decorated zinc oxide nanocomposite through a simple glycol reduction method. The silver nanoparticle-decorated zinc oxide nanocomposite-based pencil graphite electrode has been validated as a perceptive electrochemical sensing podium towards nitrite. The morphology of the prepared nanocomposite has been characterized via specific spectroscopic and electrochemical techniques. The sensor exhibits a notable enhancement in the cyclic voltammetric response to nitrite oxidation at an ideal peak potential of 0.76 V in pH 6.0 acetate buffer. Under optimum conditions of nitrite directly expanded with their concentration in the range from 30 to 1400 μM with a detection limit of 14 μM.

The objective of this study was to develop a simultaneous method for 8 amino acids including alanine, arginine, glutathione, lysine, ornithine, methionine, threonine and tryptophan in veterinary products using LC-MS/MS. To optimize MS analytical condition of 8 amino acids, each parameter was established by multiple reaction monitoring in positive mode. The chromatogram separation was achieved on a C18 column with mobile phase of 0.1% formic acid in D.W. and 0.1% formic acid in acetonitrile for green technology at a flow rate of 0.4mL/min for 5 min with gradient elution. The developed method was validated for mass accuracy, precision, linearity in veterinary products. Calibration curves were linear over the calibration ranges (0.5 – 10 mg/L) for all the analytes r2>0.99. Average recoveries were 92.96 – 105.61% and relative standard deviations (RSD) were 0.27 – 3.5%. The limit of detection (LOD) and the limit of quantification (LOQ) were 0.04 – 0.83 mg/L and 0.12 – 2.52 mg/L, respectively. All values were corresponded with the criteria ranges requested by CD 2002/657/EC. The application of this method will be helpful in quality control analysis of amino acids in veterinary products.

To understand how to efficiently observe the biomass and community of phytoplankton, phytoplankton sampling was carried out from June to October 2019 at the Yeongju dam sediment control reservoir (YJ) and Bohyeonsan dam reservoir (BH1 and BH2). The results derived from microscopic observation, such as the conventional phytoplankton qualitative/quantitative analysis, and from the CHEMTAX method based on the pigments, were compared. The relative contribution of phytoplankton, calculated by the microscopy and CHEMTAX methods, showed a significant difference in all four classes: cryptophyta, chlorophyta, cyanobacteria, and diatoms. In addition, the correlation between the two observation methods was poor. This might be caused by methodological differences in microscopy that do not consider the varying cell sizes among phytoplankton species. In this study, by converting the cells into carbon, the slope between both carbon biomasses based on microscopy and CHEMTAX was improved close to the 1 : 1 line, and the y-intercept was closer to 0 for cryptophyta and diatoms. For cyanobacteria, the slope increased, the y-intercept decreased, and the plot approached 1 : 1 although the correlation coefficients were not improved in all classes. The present study suggests that application of CHEMTAX based on pigment analysis could be a possible approach to efficiently determine the relative carbon proportions of individual classes of phytoplankton community composition.

식품첨가물로 사용되는 알긴산나트륨은 알긴산염류로서 안정제, 증점제, 유화제 등의 기능을 한다. 알긴산나트륨의 정량법은 전처리가 복잡하고 분석시간이 많이 소요되어 상대적으로 간편하고 보편적인 분석법 연구가 요구되고 있 다. 분석장비로는 HPLC-UVD 및 Unison US-Phenyl 컬럼을 사용하였으며, 전처리 조건으로 진탕기를 이용하여 실온에서 150 rpm으로 180분간 추출하였다. 알긴산나트륨의 표준 용액을 5개 농도 범위에서 검량선을 작성한 결과 직선성(R2)은 평균 0.9999로 측정되었으며 검출한계(LOD) 및 정량한계(LOQ)는 각각 3.96 mg/kg, 12.0 mg/kg이었다. 또한, 천사채를 이용해 얻은 일내 및 일간 평균 회수율과 정밀도는 각각 98.47-103.74%, 1.69-3.08 RSD%이고, 빙과류에 대한 일 내 및 일간 평균 회수율과 정밀도는 각각 99.95-105.76%, 0.59-3.63 RSD%이다. 상대불확도%는 CODEX의 기준에 적합한 1.5-7.9%의 결과를 나타냈다. 본 연구에서 확립한 방법의 적용성 검토를 위해 총 103개 품목에 대한 알긴산나트륨의 함량을 정량한 결과 당면, 유탕면, 당류가공품 유형 순으로 높은 검출율을 보였다.

최저임금은 근로자가 인간다운 삶을 영위하기 위한 최소한의 임금을 말하며, 인간다운 삶이란 기본적인 의·식·주를 누리는 것 외에 사회적·문화적 활동을 영위하는 것도 포함한다. 이러한 생활을 보장하기 위해서는 최소한의 임금이 보장되어야 하지만, 현실적으로 여러 이해당사자들 간의 충돌과 불평등으로 인 하여 최저임금을 보장받지 못하는 계층이 발생하게 되는 사회 현상이 발생하게 되었고, 이로 인하여 최저임금을 법으로 보장해야 한다는 사회적 요구가 발생 하게 되었다. 우리나라 헌법에서는 최저임금제도의 시행을 명시적으로 규정하 고 있으며, 최저임금법을 통해서 최저임금을 결정하도록 하고 있다. 이에 따라 일반근로자의 최저임금은 최저임금법을 근거로 하여 설치된 고용노동부 산하 최저임금위원회를 통해 심의 및 결정이 이루어지고 있다. 그러나 최저임금법은 선원과 선원을 사용하는 선박의 소유자를 적용범위에 포함되지 않는다고 규정하고 있다. 이로 인해 선원의 최저임금은 선원법을 근 거로 하여 매년 고시하고 있으나, 최저임금 결정을 위한 심의절차나 기준에 대 해서 구체적으로 규정하고 있지 않다. 선원최저임금이 해운산업 및 선원사회에 미치는 영향력이 커져가고 있음에 따라 객관성과 정당성을 담보할 수 있는 결 정절차의 마련이 시급하게 필요한 상황이다. 따라서 이 연구는 선원최저임금 결정절차와 관련된 문제점을 검토하고, 선원 법의 개선방안을 제시하는 것을 목적으로 한다. 이를 위해 최저임금법상 최저 임금제도와 선원법상 최저임금제도를 비교ㆍ분석하였으며, 주요 문제점을 검토 하였다. 또한 선원최저임금 결정을 위한 정책ㆍ입법적 개선방안을 제시하였다.