• 대한화장품학회지
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• 제19권1호
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• pp.1-19
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• 1993

GC/MS는 GC의 분리능과 질량분석기의 화합물의 확인 능력을 결합시킨 기기이다. 질량분석기는 1) 시료를 주입하는 시료 주입부 2) 이온을 형성시키는 ion source 3) 이온을 질량 대 하전비로 분리하는 질량 분석관 4) 분리된 이온을 감지하고 신호를 증폭하는 검출기 5) 검출된 신호로부터 질량스펙트럼을 만들고 데이터를 처리하는 데이터 시스템으로 구성된다. GC/MS는 혼합물을 GC로 분석하여 MS를 반복적으로 주사함으로써 시간에 따른 크로마토그램을 얻은 후 각 성분의 질량스펙트럼으로부터 물질 구조를 확인하는 scan mode와 특정 성분을 높은 감도로서 정량할 수 있는 SIM mode를 수행한다. GC/MS를 이용한 화장품 분석의 예로서 로션, 크림화운데이션, 염모제중의 휘발성분 분석과 비누중의 지방산 분석, 그리고 head space sampler/GC/MS를 이용한 치약 중의 휘발성분 분석 결과를 소개하였다.

• Food Science and Biotechnology
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• 제15권6호
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• pp.959-966
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• 2006

The electron-capture detector (ECD) of gas chromatographs (GC) has been used widely in pesticide analysis. However, as ECD relies on radioactive material, it is troublesome to purchase and maintain. Therefore, potent replacements for ECD were investigated. A Pulsed-discharge detector (PDD) for ECD was tested and the analytical results of PDD (ECD mode), ${\mu}ECD$, and nitrogen-phosphorus detector (NPD) were compared for 107 pesticides including organochroline, organophosphorus, pyrethroids etc. The number of pesticides identified at the lowest limit of detection (LOD) was 36, 29, and 2 for PDD, ${\mu}ECD$, and NPD, respectively. The remaining pesticides showed same response to PDD and ${\mu}ECD$. The GC-PDD analysis of pesticides spiked into representative agricultural products (brown rice, spinach, and mandarin oranges) also showed good and/or equivalent recoveries using $GC-{\mu}ECD$.

• 약학회지
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• 제26권2호
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• pp.129-132
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• 1982

A GC/MS method was developed to analyze phenolic acid extract from tobacco leaf. Extracted acids were converted to their methyl esters by refluxing with 3M hydrogen chloride in methanol, and the esters were reacted with his (trimethylsilyl) trifluoroacetamide plus 10% trimethylchlorosilane to silylate the phenolic groups. Derivatives of standard salicylic, p-hydroxybenzoic, vanillic, gentisic, p-coumaric, syringic, ferulic, and sinapic acids prepared by this procedure were analyzed by GC/MS on $20m{\times}0.2mm$ column of SE-54 glass capillary. GC/MS analysis of the extract from tobacco leaf revealed the presence of salicylic, p-hydtoxybenzoic, vanillic, gentisic, protocatechuic, p-coumaric, syringic, gallic, ferulic, caffeic, sinapic, and quinic acids, respectively. The quantitative analysis of these phenolic acids were achieved by using multiple ion selection technique.

• Bulletin of the Korean Chemical Society
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• 제18권7호
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• pp.695-702
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• 1997

The objective of this work is to determine the sugar profiles in commercial fruit juices, and to obtain chemometric characteristics. Sugar compositions of fruit juices were determined by HPLC-RID and GC-FID via methoxymation and trimethylsilylation with BSTFA. The appearance of multiple peaks in GC analysis for carbohydrates was disadvantageous as described in earlier literatures. Fructose, glucose, and sucrose were major carbohydrates in most fruit juices. Glucose/fructose ratios obtained by GC were lower than those by HPLC. Orange juices are similar to pineapple juices in the sugar profiles. However, grape juices are characterized by its lower or no detectable sucrose content. In addition, it was also found that unsweeten juices contained considerable level of sucrose. Chemometric technique such as principal components analysis was applied to provide an overview of the distinguishability of fruit juices based on HPLC or GC data. Principal components plot showed that different fruit juices grouped into distinct cluster. Principal components analysis was very useful in fruit juices industry for many aspects such as pattern recognition, detection of adulterants, and quality evaluation.

• Bulletin of the Korean Chemical Society
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• 제28권12호
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• pp.2293-2298
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• 2007

In this study, a dithizone extraction technique involving purge & trap GC-MS was developed for the determination of methylmercury in biological samples, especially blood and fish. After alkaline digestion, methylmercury in biological samples was extracted into dithizone and back-extracted into aqueous sulfide solution. The extracted methylmercury was converted to the volatile ethyl derivative, purged and trapped onto a solid-phase collection medium, and then introduced into the GC-MS system. The determined MDLs of the established method were 0.9 ng·g?1 for biological samples and its accuracy and precision were found to be 93% and 3.8%, respectively. The method was validated by analysis of CRMs such as SRM 966, BCR 463 and IAEA 407 and all analytical results were within certified ranges with average RSDs of less than 6%. The analytical results of field-sampled fish also showed that the method can be successfully used as an alternative for commonly used distillation method followed by GC-CVAFS detection.

• 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.

• 보존과학회지
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• 제33권5호
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• pp.345-354
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• 2017

전남 진도군 소재 사찰의 보수 공사 중 벽화가 발견되어 제작기법 파악을 위해 교착제로 사용된 물질을 확인하고자 하였다. 이에 해당 벽화 시편에 대해 열분해/GC/MS와 IR 분석을 실시하였으며, 열분해/GC/MS분석은 직접 열분해와 온라인 메틸화법을 도입하였다. IR 분석에서 아교, 옻, 황칠 등 전통 교착제와 초산아크릴계 수지의 스펙트럼을 벽화시편과 비교했을 때 유사하지 않았으며, 건성유인 아마인유와 비교했을 때도 유사도가 낮았다. 벽화시편의 열분해/GC/MS 분석 결과를 옻, 황칠, 아교, 초산아크릴수지와 비교했을 때 이들 물질이 아닌 것으로 나타났다. 한편, 벽화시편에서 팔미트산, 옥타데칸산, nonanedioic acid, 옥타데센산 등 건성유에 특징적인 물질이 검출되었고, 경화 건성유와 유사한 열분해/GC/MS 크로마토그램이 관찰되었다. 따라서, 벽화는 건성유를 교착제로 사용하여 제작된 것으로 판단되었다.

• 한국식품위생안전성학회지
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• 제7권1호
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• pp.45-48
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• 1992

우리나라의 식품 공전에서 주류의 검사방법이 비색 및 적정의 방법으로 나타나 있다. 그러나 이런 습식분석법은 시간이 많이 걸리고 개인오차 등 심각한 문제를 내포하고 있다. 주류의 제조 과정 중 휴겔류가 생성되는데 n-propanol, 2-propanol, n-butanol, i-butanol, i-amyl alcohol이 주로 생성된다. 우리는 GC를 이용하여 개개의 물질을 분리하고 농도에 따른 신호가 직선성이 얻어지면 동시에 정성 및 정량 자료를 얻을 수 있다. 즉 GC나 GC/MSD에 의해 capillary FFAP 칼럼을 이용하여, 다섯가지 휴젤성분, 아세트알데히드, 메탄올, 에탄올 그리고 내부표준물질인 아세토니트릴을 동시에 분리하였다. 그리고 capillary FFAP 칼럼으로 분리된 각 피이크가 단일종이라는 것을 GC/MSD를 이용하여 각각의 mass 스펙트럼으로 확인할 수 있었다. 또한 내부 표준법으로 GC에 의해 각 물질에 대한 좋은 정량자료를 얻었다.

• 식물병연구
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• 제21권4호
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• pp.280-289
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• 2015

옥수수는 세계적으로 가장 중요한 작물이다. 옥수수의 소비가 꾸준히 증가하고 있지만, 생산량은 연작과 Fusarium spp.와 같은 토양전염성 곰팡이병의 감염에 의해 줄어들고 있다. 최근에 우리나라를 포함해 전 세계적으로 F. subglutinans와 F. temperatum에 의해 발생되는 옥수수 밑둥썩음병의 발생이 많이 보고되고 있다. 본 연구에서는 병에 걸리지 않은 건전한 옥수수 토양 근권에서 F. subglutinans와 F. temperatum에 대치배양을 통해 항균활성을 보이는 3 균주(GC02, GC07, GC08)를 선발하였다. 선발된 3 균주 중 GC02와 GC07이 균사생장을 효과적으로 억제하였다. 그리고 16s rRNA에 기반하여 분석한 결과, GC02는 Bacillus methylotrophicus, GC07은 B. amyloliquefaciens 그리고 GC08은 B. thuringiensis로 동정되었다. 또한, GC02와 GC07은 포자발아의 억제에도 효과적이었다. 3개의 Bacillus 균주들은 모두 protease의 활성이 강하게 나타났으며, cellulase 활성은 GC07과 GC08에서만 나타났다. 그리고 불용성 인산의 가용화와 siderophore의 생산은 GC02와 GC07이 비교적 GC08에 비해 우수한 것으로 나타났다. 옥수수 줄기에 2개의 Fusarium과 접종하여 발병억제효과를 검정한 결과 B. amyloliquefaciens GC07이 가장 효과적인 방제효과를 나타내었다. 또한 B. methylotrophicus GC02와 B. amyloliquefaciens GC07은 다른 식물병원성 진균들도 효과적으로 균사생장을 억제하였다. 따라서, B. methylotrophicus GC02와 B. amyloliquefaciens GC07은 식물병원성 진균방제에 생물학적 방제제로서 역할이 가능하다고 판단된다.

• Mass Spectrometry Letters
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• 제4권1호
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• pp.18-20
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• 2013

Headspace solid phase micro-extraction gas chromatography/flame ionization detection (HS-SPME-GC/FID) method was compared with headspace gas chromatography/mass selective detection (HS-GC/MS). Organic solvent-spiked urine as well as urine samples from workspace was analyzed under optimal condition of each method. Detection limit of each compound by HS-SPME-GC/FID was $3.4-9.5{\mu}g/L$, which enabled trace analysis of organic solvents in urine. Linear range of each organic solvent was $10-400{\mu}g/L$, with fair correlation coefficient between 0.992 and 0.999. The detection sensitivity was 4 times better than HS-GC/MS in selected ion monitoring (SIM) mode. Accuracy and precision was confirmed using commercial reference material, with accuracy around 90% and precision less than 4.6% of coefficient of variance. Among 48 urine samples from workplace, toluene was detected from 45 samples in the range of $20-324{\mu}g/L$, but no other solvents were found. As a method for trace analysis, SPME HS GC/FID showed high sensitivity for biological monitoring of organic solvent in urine.