• 제목/요약/키워드: GC and GC-MS method

검색결과 828건 처리시간 0.026초

GC-MS를 이용한 식물홀몬 분석 (Analysis of Plant Hormones using GC-MS)

  • 조광연
    • 한국작물학회지
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    • 제34권s01호
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    • pp.26-32
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    • 1989
  • The analytic principles of GC and MS were explained in relation to plant hormone analyses and the characteristics of two instruments were compared. The selection of column, condition of measurement and the method of ionization to get a good spectrum were also briefly described. Finally, the pre-treatment of sample by solvent extraction method to remove the unnecessary part of sample and the synthetic method, especially reagents and reaction condition, for the preparation of ether or ester derivative which can be easily vaporized in GC were explained.

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GC/FID와 GC/MS 분석법에 의한 목질제품에서의 VOC 방출특성 비교 (The Comparison of VOC Characteristics Emitted from Wood-based Panels Using GC/FID and GC/MS)

  • 황윤서;박현주;손윤석;김조천
    • 한국대기환경학회지
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    • 제27권4호
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    • pp.436-442
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    • 2011
  • In this study, the Total Volatile Organic Compounds (TVOC) emitted from wood-based panels were compared by two analytical methods using the GC/FID and the GC/MS. Japanese Larch, Yellow Poplar, Particle Board (PB) and Medium Density Fiberboard (MDF) were selected as target materials. Major compounds emitted from the panels were Toluene, ${\alpha}$-pinene, ${\beta}$-pinene and limonene. In case of TVOC using GC/FID method, MDF E2 (1,497 ${\mu}g/m^3$) revealed the highest concentration among all wood-based panels, while Japanese Larch (1,772 ${\mu}g/m^3$) showed the highest value with respect to GC/MS method. Furthermore, it was found that the amount of VOC emitted from panels was different depending upon analytical methods. This significant difference was attributed to analytical sensitivities of GC/FID and GC/MS for various VOC. Besides, it was found that the composition ratios of main VOC compounds were not significantly different.

PAHs 농도 분포에 따른 GC/MS와 HPLC의 분석특성에 관한 연구 (Analytical Characteristics of GC/MS and HPLC according to the Concentration Distribution of PAHs)

  • 홍좌령;최광민
    • 한국산업보건학회지
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    • 제25권3호
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    • pp.312-321
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    • 2015
  • Objectives: The purpose of this study was to determine the best method to analyze PAHs at extremely low concentrations. To this end, 16 PAHswere analyzed simultaneously by GC/MS, HPLC/FLD and HPLC/UVD, and the analytical characteristics of HPLC and GC/MS were compared. Methods: This study was conducted by GC/MS and HPLC/FLD/UVD, and evaluated linearity, precision and detection limit. Standard solutions were prepared for 21 samples in the range of $0.00001{\sim}1.0{\mu}g/mL$ and the samples were divided into four groups. All samples were made in three sets and analysis was replicated seven times. Results: Sixteen PAHs could be simultaneously separated by HPLC and GC/MS, and the adequate equipment was HPLC/FLD. The retention times by HPLC were shorter than GC/MS, and HPLC had better separation for most PAHs than GC/MS. The peaks of naphthalene and naphthalene-D8 partially overlapped for GC/MS. HPLC/FLD had a 20-2000 times lower limit of detection than GC/MS and UVD. However FLD was not adequate for analyzing acenaphthylene because it has too low a fluorescence quantum yield to be detected. The precision of HPLC/FLD/UVD and GC/MS showed less than 20% at $0.001{\mu}g/mL$ PAHs and when the concentration was higher, the coefficient of variation was decreased. HPLC/FLD was better for the overall detection of limits. Conclusions: The results indicate that the HPLC/FLD method has good linear range, precision and a detection of limits from $0.00001{\sim}0.0001{\mu}g/mL$ for all 16 PAHs. This study contributes to providing useful data for analysis technology and can be applied to occupational exposure measurement for PAHs in workplaces.

GC-MS/MS와 LC-MS/MS를 이용한 생약재 중 261종 농약의 동시분석 (Development of Multi-residue Analytical Method for 261 Pesticides in Herbal Medicines using GC-MS/MS and LC-MS/MS)

  • 나은식;김성수;홍성수;김경주;이용재;이병철;이규승
    • 한국환경농학회지
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    • 제39권2호
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    • pp.142-169
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    • 2020
  • BACKGROUND: A new analytical method has been developed to determine 261 pesticide residues in herbal medicines. METHODS AND RESULTS: The extraction of pesticides was carried out by modified method of the Korea Food Standards Codex sample extraction and determination was performed using GC-MS/MS and LC-MS/MS. During the pre-treatment process of the test method, Solid-liquid separation was changed to centrifugation. The method was validated by the precision and accuracy results. 261 pesticides spiked at three level 20, 50, 100 ug/kg in herbal medicines. The limit of quantification of method were 4-40 ug/kg for GC-MS/MS and 2-45 ug/kg for LC-MS/MS, respectively. Among the pesticides analysed by GC-MS/MS and LC-MS/MS, 244 pesticides (94% of total number) in chinese matrimony vine and 224 pesticides (86% of total number) in korean angelica root and 231 pesticides (89% of total number) in jujube and 214 (82% of total number) in cnidium showed recoveries in the range of 70-120% with RSD⪯20%. CONCLUSION: These results indicated that GC-MS/MS and LC-MS/MS analysis with the sample extraction in this study can be applied to multi-residue analysis of pesticides in herbal medicines.

GC/ECD 및 GC/MS을 이용한 토양 중 PCBs 분석방법 고찰 (Analytical method of the polychlorinated biphenyls in soil using GC/ECD and GC/MS)

  • 김태승;신선경;윤정기;김종하;김형섭;이정아
    • 분석과학
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    • 제20권2호
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    • pp.91-108
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    • 2007
  • 토양 중 PCBs 분석방법을 검토하기 위해 우리나라 토양오염공정시험방법 및 선진국의 분석방법을 비교 검토하고 결과를 근거로, 추출 및 전처리방법, 칼럼정제방법, 분석용 칼럼 조건, 기기분석 조건 및 정량방법을 검토하였다. 또한 검토된 방법에 따라 토양 중 PCBs 세부분석지침(안)을 제시하고, 제시된 세부분석지침(안)에 의해 PCBs 제품으로 오염시킨 토양 5건 시료와 토지이용도별 및 오염원별 23건의 시료를 전처리하여 분석하였다. 기체크로마토그래피/전자포획검출법(GC/ECD)에 의한 토지이용도별 및 오염원별 PCBs 분석결과는 모든 시료에서 피크패턴(GC/ECD)을 확인 할 수 없었으나, 기체크로마토그래피/질량분석법(GC/MS)에 의한 개별이성체 정량결과는 $0.002{\sim}0.487{\mu}g/kg$ 범위로 검출되었다.

EI-GC/MS/MS를 이용한 니트로사민류의 수질분석 (Determination of N-nitrosamines in Water by Gas Chromatography Coupled with Electron Impact Ionization Tandem Mass Spectrometry)

  • 이기창;박재형;이원태
    • 대한환경공학회지
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    • 제36권11호
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    • pp.764-770
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    • 2014
  • 본 연구는 electron impact-gas chromatography/mass spectrometer (EI-GC/MS)를 이용하여 N-nitrosamines 분석하는 방법의 분리성, 정성 및 정량적 유효성을 평가하였다. 극미량의 검출을 위해 시료전처리는 자동고상추출과 질소농축과정을 거쳐 수행하였다. 표준시료를 전처리 없이 EI-GC/MS (SIM)와 EI-GC/MS/MS (MRM)를 이용하여 직접 분석한 결과, 두 방법 모두 유사한 감응도를 보였다. 반면, 전처리한 표준시료를 EI-GC/MS로 분석한 경우 불순물 피크에 의한 간섭영향에 의해 낮은 ng/L 수준의 정량은 어려운 것으로 나타났다. 8종의 N-nitrosamines에 대한 EI-GC/MS/MS 분석결과, 방법검출한계 및 정량한계는 각각 0.76~2.09 ng/L, 2.41~6.65 ng/L 수준으로 기존 분석방법에 비하여 낮게 나타났다. 첨가농도 10, 20, 100 ng/L에 대한 실험에서 정밀도(1.2~13.6%)와 정확도(80.4~121.8%) 모두 만족하였으며, 검량선의 직선성에 대한 결정계수($R^2$)도 0.999 이상이었다. 환경시료에 대한 대체표준물질(NDPA-$d_{14}$)의 회수율도 86.2~122.3%을 나타내어, 본 연구에서 평가된 방법으로 N-nitrosamines의 정밀분석이 가능함을 검증하였다.

Analysis of Agrochemical Residues in Tobacco Using QuEChERS Method by GC-MS/MS

  • Lee, Jeong-Min;Jang, Gi-Chul;Hwang, Keon-Joong
    • 한국연초학회지
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    • 제29권2호
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    • pp.132-139
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    • 2007
  • This study was performed to apply the more rapid and accurate sample preparation, and the high selectivity and sensitivity of the analyte detection by gas chromatography-triple quadrupole mass spectrometry (GC-MS/MS). QuEChERS (quick, easy, cheap, effective, rugged and safe) method was validated for 49 agrochemicals in the CORESTA Agrochemical Advisory Committee guide and amenable to GC-MS/MS determination. In QuEChERS method, the effects of sorbents (PSA, $C_{18}$ and GCB) and matrix of the analytes in tobacco types (flue-cured, burley and oriental) were investigated. MS/MS acquisition provided high specificity and selectivity for agrochemicals and low limit of quantification. QuEChERS by using PSA alone and the matrix-matched standards gave good recoveries and RSD values in three types of tobaccos. QuEChERS method was no needed to be complex clean-up procedure and would be used as the fast and easy method for agrochemical residue analysis in tobacco.

LC-MS/MS와 GC-MS/MS를 이용한 사과와 쌀 시료에서 320종 농약의 다성분 분석 (Development of Multi-residue Analysis of 320 Pesticides in Apple and Rice Using LC-MS/MS and GC-MS/MS)

  • 김종환;김영진;권영상;서종수
    • 농약과학회지
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    • 제20권2호
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    • pp.104-127
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    • 2016
  • 본 연구는 사과와 쌀에서 320성분 농약에 대한 다성분 동시분석법을 확립하고자 수행되었다. 시료의 추출은 QuEChERS법을 사용하였고, 추출 후 잔류물은 LC-MS/MS와 GC-MS/MS로 기기분석 하였다. 시험 농약은 LC-MS/MS 251성분, GC-MS/MS 110성분을 선발하였으며, 41성분은 공통적으로 적용되었다. 분석법의 정량한계는 LC-MS/MS에서 $0.01{\sim}20{\mu}g/kg$, GC-MS/MS에서 $0.1{\sim}100{\mu}g/kg$으로 산출되었다. 사과와 쌀에서 회수율 70~120%, 상대표준편차 20% 이내의 조건을 충족한 성분은 LC-MS/MS로 분석한 농약 중 각각 242성분(96%)과 237성분(94%)로 나타났으며, GC-MS/MS로 분석한 농약 중에는 각각 103성분(94%)과 83성분(76%)로 나타났다. 본 연구를 통해 QuEChERS 전처리와 LC-MS/MS 및 GC-MS/MS를 이용한 분석법은 농산물(사과 및 쌀) 중 잔류농약 다성분 동시 분석에 효과적으로 적용될 것으로 기대된다.

GC/MS와 GC/ECD를 이용한 한약재 중 잔류 농약의 분석 (GC/MS and GC/ECD Analysis of Residual Pesticides in Herbal drugs)

  • 김호경;박소연;고병섭
    • 대한한의학회지
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    • 제20권1호
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    • pp.44-51
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    • 1999
  • Analysis of residual pesticides in herbal drugs was performed by GC-ECD and GC-MS. Especially, selected ion monitoring(SIM) technique was applied to increase the GC/MS sensitivity. Analysis of residual pesticides was determined sensitivity and selectively without any internal standard by setting the SIM technique to their characteristic fragments for quantitation ion and confirmation ion. The combination of two detector, GC-ECD and MS-SIM technique, is abailable for determining a multiclass residual pesticides in herbal drugs. The average recoveries through the method were $65.9%{\sim}99.7%$ in herbal drugs. The data of gas chromatographic analysis was compared with the limits of residual pesticides in herbal drugs and agricultural foods. 4. 4-DDT was detected above the limits to the residual pesticides in herbal drugs. Diazinon and EPN were detected, but the limits of residual pesticides were less than that of agricultural foods.

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GC-MS/MS를 이용한 한강수계 및 상수도계통에서 N-nitrosamines 조사 (Investigation of N-nitrosamines using GC-MS/MS in Han-river Water Supply Systems)

  • 윤우현;이준호;이현주;이수원;안재찬;김복순
    • 한국물환경학회지
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    • 제32권5호
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    • pp.410-418
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    • 2016
  • This study was conducted to improve the analysis method used for N-nitrosamines and to investigate the occurrences of N-nitrosamines in tributaries of the Han-river, intake stations, water treatment plants and tap water used within the city of Seoul. The samples were pretreated through a solid phase extraction and analyzed using a gas chromatography tandem mass spectrometer (GC-MS/MS). The GC-MS/MS in CI mode was compared with the GC-MS/MS in EI mode by the method detection limits (MDLs). MDLs by GC-CI/MS/MS and GC-EI/MS/MS were 0.2 ~ 1.1 ng/L and 0.2 ~ 1.4 ng/L, respectively. Samples were collected from ten tributaries of the Han-river (T1 ~ T10), six intake stations (I1 ~ I6), six water treatment plants (P1 ~ P6) and 25 taps in Seoul city. The maximum levels of N-nitrosodimethylamine (NDMA) were 0.013 μg/L, 0.008 μg/L, 0.006 μg/L and 0.002 μg/L in tributary water, raw water, finished water and tap water samples, respectively. Detected levels were much lower than 0.1 μg/L corresponding to the guideline value of WHO.