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연안환경 괭이갈매기(Larus crassirostris) 알의 DDTs 및 수은 농도분포 조사
최정희 ( Jeong-heui Choi ),정다위 ( David Chung ),이종천 ( Jongchun Lee ) 한국환경과학회 2018 한국환경과학회지 Vol.27 No.12
Sea gulls are high trophic level consumers in the coastal environment, and thus, which have been widely used to monitor contamination biomagnified through a food web. However, such monitoring studies using sea gulls have been rare in the Korean literature. The National Environmental Specimen Bank chose eggs of a black-tailed gulls (Larus crassirostris) to serve as an environmental specimen for the long-term monitoring of the coastal ecosystem affected by terrestrial pollutants. Black-tailed gull eggs were collected from Baengnyeongdo, Hongdo and Uleungdo, and their DDTs and total mercury content were determined. The highest concentration of ∑DDTs was 231.6±106.1 μg/kg wet in Baengnyeongdo, followed by 230.0±123.8 μg/kg wet in Ulleungdo, and 117.7±18.3 μg/kg wet in Hongdo. In addition, total mercury was detected at 414.5±97.6 μg/kg wet in Ulleungdo, 363.9±123.6 μg/kg wet in Hongdo, and 237.5±42.3 μg/kg wet in Baengnyeongdo. Relatively high concentrations of the target pollutants were recorded in specimens from Ulleungdo. Additional comprehensive and prolonged studies are required to elucidate spatial and temporal patterns of contamination in black-tailed gull eggs with regard to monitoring contaminant trends in eggs and prey.
04 포스터 발표 : 환경 화학 분야(PC) ; PC-13 : 농경지 토양과 농자재 중 축산용 항생제 잔류기준 설정을 위한 기초연구
최정희 ( Jeong Heui Choi ),이영준 ( Young Jun Lee ),정형석 ( Hyung Suk Chung ),심재한 ( Jae Han Shim ) 한국환경농학회 2015 한국환경농학회 학술대회집 Vol.2015 No.-
Maximum residue limits are the fundamental and essential regulatory means to investigate and secure food safety against pesticides and heavy metals. The importance of these actions has been emphasized along with concerns over consistent pollution of the environment that can be named as a cradle for food production. Agricultural fields are no exception on the pollution. The pollution of agricultural fields might be rather accelerated since diverse inputs including synthetic and/or natural fertilizers and crop protectants are applied to the fields to increase productivity. Korean authorities have been actively encouraging the use of an organic fertilizer, whereas it is afraid that substantive institutional strategies for safety of the organic fertilizers are rare. An 88.7% of livestock excretions was recycled for organic fertilizers in 2012, Republic of Korea; however, it is hard to ensure safety of the organic fertilizers if we consider that most of the reused excretions is from concentrated animal feeding operations using veterinary drugs a lot generally. In order to produce real safe agricultural commodities, safety of agricultural soil and organic fertilizers should be indispensible. Therefore, tolerance of veterinary antibiotics in agricultural soils and materials is necessary, and this is a fundamental study for it. The amounts of livestock excretions and antibiotics on domestic animal species, and of solid/liquid manure produced, and past monitoring outcomes were investigated basically, finally resulting in tetracycline, chlortetracycline, oxytetracycline, sulfamethazine, sulfamethoxazole, sulfathiazole, amoxicillin, ampicillin, enrofloxacin, salinomycin, tylosin, florfenicol, tiamulin, dihydrostreptomycin, ceftiofur, clopidol, and monensin as a target veterinary antibiotics for monitoring of solid/liquid manures and soils.
유도체화 반응에 의한 현미 중 thiosultap의 분석
최정희(Jeong-Heui Choi),도정아(Jung-Ah Do),윤혜정(Hae-Jung Yoon),박용춘(Yong-Chun Park),김재훈(Jae Hun Kim),최동미(Dongmi Choi) 한국농약과학회 2010 농약과학회지 Vol.14 No.1
Thiosultap, a nereistoxin analog insecticide, registered in China has been used to control selected beetles and Lepidopteran pests on rice, vegetables and fruit trees. Although domestic use of thiosultap is not permitted, it is needed to monitor this insecticide from imported crops because that has been used on crops in many foreign countries, especially China. Thiosultap in hulled rice was determined as nereistoxin derived in basic condition by GC-FPD. This method accomplished ion-associated liquid-liquid partitioning for cleanup, and limit of quantification and linearity performed by the established method were 0.05 ㎎ ㎏?¹ and 0.995(r²). The recoveries performed by control hulled rice fortified with thiosultap at 0.5 and 2.5 ㎎ ㎏?¹ were 96.1±7.9~ 100.8±6.1%.
GC-MS 를 이용한 하천수 중 Bisphenol계 화합물의 동시분석 및 모니터링
김지현,최정희,강태우,강태구,황순홍,심재한,Kim, Jihyun,Choi, Jeong-Heui,Kang, Tae-Woo,Kang, Taegu,Hwang, Soon-Hong,Shim, Jae-Han 한국환경농학회 2017 한국환경농학회지 Vol.36 No.3
본 연구는 하천수 중 bisphenol계 화합물 종 6 (BPA, BPB, BPC, BPE, BPF, BPS)을 동시분석하기 위하여 GC-MS를 이용하였다. 또한 최적의 전처리 방법을 확립하고자 SPE 및 LLE법을 이용하여 표준시료로부터 검량선의 직선성, MDL, LOQ, 정확도 및 정밀도를 비교하였다. SPE 및 LLE 전처리 방법에 의한 MDL은 각각 $0.0005{\sim}0.0234{\mu}g/L$와 $0.0037{\sim}0.2034{\mu}g/L$, LOQ는 각각 $0.0015{\sim}0.0744{\mu}g/L$와 $0.0117{\sim}0.6477{\mu}g/L$, 검량선의 결정계수($r^2$)는 모두 0.9969이상 정확도는 각각 93.2~108%와 97.4~120%, 정밀도는 각각 1.7~4.6%와 0.7~6.5%범위로 만족한 정도관리 결과를 얻었다. 하지만 SPE법에 의한 MDL 및 LOQ 값은 LLE법보다 약 4~45배 정도 높은 감도를 보였고, 특히 BPA의 경우는 다른 화합물들보다 45배 정도 높았다. 따라서, 본 연구에서는 SPE법을 적용하여 하천수 시료를 분석하였고, 조사지점은 본류 7개, 지류 6개, 하수종말처리장 2개 지점을 선정하였다. Bisphenol계 화합물 중에서 BPB, BPC, BPE, BPF 및 BPS는 모두 불검출 되었으나, BPA 농도는 $0.0095{\sim}0.2583{\mu}g/L$ 범위로 본류 $0.0166{\sim}0.0810{\mu}g/L$, 지류 $0.0095{\sim}0.2583{\mu}g/L$, 하수종말처리장$0.0352{\sim}0.1217{\mu}g/L$으로 미량 수준이었다. BACKGROUND:This study was carried out to establish an efficient sample preparation for the simultaneous determination of bisphenols (BPs) in river water samples using gas chromatography-mass spectrometry (GC-MS). Sample preparation was examined with conventional extraction methods, such as solid-phase extraction (SPE) and liquid-liquid extraction (LLE), and their efficiency was compared with validation results, including linearity of calibration curve, method detection limit (MDL), limit of quantification (LOQ), accuracy, and precision. METHODS AND RESULTS:The BPs (bisphenol A, BPA; bisphenol B, BPB; bisphenol C, BPC; bisphenol E, BPE; bisphenol F, BPF; bisphenol S, BPS) were analyzed using GC-MS. The range of MDLs by SPE and LLE methods was $0.0005{\sim}0.0234{\mu}g/L$ and $0.0037{\sim}0.2034{\mu}g/L$, and that of LOQs was $0.0015{\sim}0.0744{\mu}g/L$ and $0.0117{\sim}0.6477{\mu}g/L$, respectively. The calibration curve obtained from standard solution of $0.004{\sim}4.0{\mu}g/L$ (SPE) and $0.016{\sim}16{\mu}g/L$ (LLE) showed good linearity with $r^2$ value of 0.9969 over. Accuracy was 93.2~108% and 97.4~120%, and precision was 1.7~4.6% and 0.7~6.5%, respectively. The values of MDL and LOQ resulted from the SPE method were higher than those from the LLE method, particularly those values of BPA were highest among the BPs. Based on the results, the SPE method was applied to determine the BPs in river water samples. Water samples were collected from mainstream, tributary and sewage wastewater treatment plants (SWTPs) in the Yeongsan river basin. The concentration of BPB, BPC, BPE, BPF and BPS were not detected in all sites, whereas BPA was ranged $0.0095{\sim}0.2583{\mu}g/L$, which was $0.0166{\sim}0.0810{\mu}g/L$ for mainstreams, $0.0095{\sim}0.2583{\mu}g/L$ for tributaries, $0.0352{\sim}0.1217{\mu}g/L$ for SWTPs. CONCLUSION: From these results, the SPE method was very effective for the simultaneous determination of BPs in river water samples using GC-MS. We provided that it is a convenient, reliable and sensitive method enough to monitor and understand the fate of the BPs in aquatic ecosystems.
Determination of Cyhalofop-butyl and its Metabolite in Water and Soil by Liquid Chromatography
헴리나,최정희,유학,카이사티아,심재한,Hem, Lina,Choi, Jeong-Heui,Liu, Xue,Khay, Sathya,Shim, Jae-Han The Korean Society of Pesticide Science 2008 농약과학회지 Vol.12 No.4
실험실 내 조건에서, 물과 토양 중 cyhalofop-butyl과 그 대사물질인 cyhalofop acid를 위한 잔류분석법이 고감도에서도 간단하고 매우 효과적으로 개발되었다. 물과 토양 중 cyhalofop-butyl과 cyhalofop acid를 분석하기 위하여 액액분별추출과 silica gel chromatographic 정제를 수행하였으며 HPLC-UV를 이용하여 정성/정량하였다. cyhalofop-butyl의 회수율은 2 가지 농도에서 3 반복 수행하여 각각 82.5-100.0%와 66.7-97.9%이었고, 검출한계와 최소검출량은 두 시료에서 모두 0.02 ppm과 10 ng이었다. Cyhalofop acid의 회수율은 물과 토양에서 각각 80.7-104.8%와 76.9-98.1%이 었으며, 검출한계는 각각 0.005 ppm과 0.01 ppm이었고 최소검출량은 두 시료에서 모두 2 ng이었다. Cyhalofop-butyl의 반감기는 물과 토양에서 각각 4.14와 6.6 day였다. 개발되어진 본 시험법은 cyhalofop-butyl의 30% 유탁제를 처리한 물과 토양에서 그 잔류량을 분석하기 위하여 성공적으로 적용되었다. In this study, a simple, effective, and sensitive method has been developed for the quantitative residue analysis of cyhalofop-butyl and its metabolite cyhalofop acid in water and soil when kept under laboratory conditions. The content of cyholofop-butyl and cyhalofop acid in water and soil was analyzed by first purifying the compounds through liquid-liquid extraction and partitioning followed by Silica gel (adsorption) chromatography. Upon the completion of the purification step the residual levels were monitored through high-performance liquid chromatography (HPLC) using a UV absorbance detector. The recoveries of cyhalofop-butyl from three replicates spiked at two different concentrations ranged from 82.5 to 100.0% and from 66.7 to 97.9% in water and soil, respectively. The limit of detection and minimum detection level of cyhalofop-butyl in water and soil was 0.02 ppm and 10 ng, respectively. The recoveries of cyhalofop acid ranged from 80.7 to 104.8% in water and from 76.9 to 98.1 % in soil. The limit of detection of cyhalofop acid was 0.005 ppm in water and 0.01 ppm in soil, while the minimum detection level was 2 ng both in water and soil. The half-live of cyhalofop-butyl was 4.14 and 6.6 days in water and soil, respectively. The method was successfully applied to evaluate cyhalofop-butyl residues in water and soil applied aj. 30% emulsion, oil in water (EW) product.
04 포스터 발표 : 환경 화학 분야(PC) ; PC-15 : GC-μECD를 이용한 상추중 Metrafenone과 Boscalid분석을 위한 QuEChERS방법 비교
임소정 ( So Jeong Im ),무스픽 ( Md. Musfiqur Rahman ),김성우 ( Sung Woo Kim ),압두 ( A. M. Abd El-aty ),최정희 ( Jeong Heui Choi ),카빌 ( Md. Humayun Kabir ),팔하 ( Waziha Farha ),정다이 ( Da I Jung ),이영준 ( Young Jun Lee 한국환경농학회 2015 한국환경농학회 학술대회집 Vol.2015 No.-
Three versions of the QuEChERS method (quick,easy, cheap, effective, rugged and safe) . the original (unbuffered), modified acetate-buffered, and citrate-buffered versions were compared for thedetermination of metrafenone and boscalid residues in lettuce via gas chromatography-micro electron capture detector (GC-μECD). Onlymodified acetate-buffered version provided acceptable and more consistent recoveries for both of the target analytes than the other versions. Matrix matched calibration curves prepared for the analytes provided good linearity over the calibration ranges with the co-efficient of determination (r2) ≥ 0.998. Limit of detection (LOD) and quantification (LOQ) were 0.003 and 0.01 mg/kg for both of the analytes. Method was validated in triplicate at two fortification level and recovery of modified acetate buffered version was ranges between 77.0 and 88.1% with relative standard deviation (RSD) < 5 for the quantified analytes. The developed method was applied to the field incurred lettuce sample where half-life of metrafenone and boscalid were found 2.6 and 2.9 days respectively for double doses and 3.4 and 3.6 days respectively for triple doses.