• 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.

• 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.

• 한국산업보건학회지
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• 제11권3호
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• pp.206-211
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• 2001

This article describes identification and quantification of benzene in the casting process. Air samples around the casting process were taken by using personal air sampler attached charcoal tube and desorbed by carbon disulfide. The identification and quantitative analysis of benzene have been performed by GC-MS and GC-FID. Calibration range of standard solutions for benzene was prepared in range from 0.1 to 2 times of TLVs concentrations($1.4{\sim}28{\mu}g/1m{\ell}$ CS2) and the limit of detection was $0.11{\pm}0.002{\mu}g/1m{\ell}$ CS2. Benzene detected in airborne was ranged in 4.0ppb~104.7ppb.

• 한국대기환경학회:학술대회논문집
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• 한국대기환경학회 2001년도 추계학술대회 논문집
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• pp.249-250
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• 2001

최근 대도시 지역에서의 오존농도가 환경기준을 초과하는 빈도가 날로 증가하고 있는 실정이며, 이에 국내의 경우 오존농도 증가에 대비하여 대기 중 오존농도가 일정기준(시간당 0.12 ppm)보다 높게 나타났을 때 신속하게 경보를 발령, 시민들의 건강과 생활환경상의 피해를 최소화하기 위해 오존경보제를 시행해오고 있다. 한편 전세계적으로 대도시 지역에서의 지표면 오존농도가 환경기준을 초과함에 따라 오존생성과 관련된 전구물질(precursor)에 대한 제어과정이 지표면 오존농도의 저감을 실현하기 위한 가장 시급한 과제로 대두되고 있으며, 특히 미국의 경우 1993년부터 광화학평가측정망(Photochemical Assessment Monitoring Stations;PAMS)을 설치하여 이들 물질에 대한 보다 집중적인 모니터링을 실시하고 있는 것으로 알려져 있다. (중략)

• Mass Spectrometry Letters
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• 제14권4호
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• pp.160-165
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• 2023

Citronella oil, an essential oil extracted through steam distillation from the leaves and stems of Cymbopogon, is a natural complex substance (NCS) regulated by the Korean government for its use in insect repellents. The component ratios of NCSs like citronella oil vary due to differences in manufacturing processes and origins, presenting a challenge in identifying and quantifying these substances in consumer chemical products. This study analysed ten commercially available products of the most commonly used types of citronella oil, specifically Java and Ceylon types, using gas chromatography (GC)-mass spectrometry (MS) and GC with flame ionization detection (FID). Through chromatographic data, we aimed to determine the components that can qualitatively identify citronella oil and the indicator ingredients that can be used for content analysis.

• 분석과학
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• 제20권5호
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• pp.361-369
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• 2007

냉각기에서 방출되는 불쾌한 냄새는 실내 공기질을 저하시키는 주요 원인이다. 냄새문제를 해결하기 위해서는 냄새원인을 규명하여야 한다. 냉각기에서 냄새가 발생될 때 공기시료는 냄새강도는 약하고 순간적이어서 채취하여 분석하는데 많은 어려움이 따른다. 이 연구에서 응축수를 이용하여 냉각기의 냄새원인물질의 평가 가능성을 확인하였다. 응축수는 headspace-solidphase microextraction(HS-SPME) 방법을 이용하여 채취하였다. GC/FID/Olfactometry(GC/FID/O)로 냄새물질을 확인한 후, GC/AED, GC/MS로 정성하였다. 직접관능평가 결과 및 GC/FID/O의 개별냄새물질 분석 결과, 공기시료와 매우 유사하게 나타났다. 냄새원인물질은 주로 산소를 포함하는 alcohols와 acids로 확인되었다. 응축수를 이용한 냄새원인물질 평가 방법은 채취 용이성, 비용, 분석적인 측면에서 효과적인 방법으로 평가 되었다.

• 분석과학
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• 제14권3호
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• pp.274-285
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• 2001

본 연구는 ppb와 ppt 정도의 농도 수준으로 존재하고 있는 대기 중 휘발성 유기화합물을 분석하기 위해 열탈착-저온농축-GC/FID/FPD를 개발하였다. 그리고 고체흡착제가 충진된 흡착관과 자체 제작한 휴대용 가스채취기를 사용하여 강원도 춘천지역에 위치한 근화동과 혈동리 생활폐기물 매립장에서 배출되는 VOCs를 채취하였다. 저온농축방법으로는 분석컬럼을 직접 저온 농축하는 on-column 저온 농축장치와 0.8mm loop를 이용한 저온농축장치를 서로 비교 검토해 보았다. On-column 저온농축법은 loop에 비해 분리능은 좋으나 흡착관에 채취한 시료를 저온농축할 때 요구되는 50 psi의 높은 탈착압력으로 인해 흡착관의 SwageLok fitting이 마모되어 가스가 새는 문제점이 발생하였다. 이에 반해 탈착압력을 낮추고 탈착유량을 늘리기 위해 설계한 loop 경우에는 탈착압력이 0.4 psi로 on-column에 비해 매우 낮아 가스가 새는 것을 방지할 수 있었다. 열탈착-저온농축-GC/FID/FPD로 분석한 근화동과 혈동리 생활폐기물 매립장에서 검출된 물질로는 toluene, xylene, ethylbenzene등 탄화수소류와 악취물인 styrene, limonene, dimethyl disulfide 등이 검출되었다. 그리고 매립지에서 방출되는 VOCs는 매립되는 폐기물의 조성과 매립기간에 따라 다르게 나타났다. 검출된 화합물은 저온농축-GC/MS를 이용하여 확인하였다.

• Archives of Pharmacal Research
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• 제16권3호
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• pp.175-179
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• 1993

Gas chromoatography with flame ionization detector (FID) along with mass spectrometry (GC/MS) were used for the screening and quantification of methamphetamine (MA) and its major metabolite, amphetamine (AM0, in blood and urine in eleven fatal cases in which MA abuse was suspected. Postmortem blood MA varied from $0.5-30.2\;\mu{g/ml}$, while Am levels ranged from none detected (6 of 11 cases) to 4.8 .mu.g/ml. Additionally, distribution studies were performed in three of these cases in which tissue smaples were available for evaluation. Liver contained the highest ocncentration of MA among the tissu samples. In eight of the eleven cases, when no other direct cause of death was evident (i.e. 3 cases of traumatic dath0, either no blood AM was found or the ratio of MA/AM was 3.4 or greater. These data are consistent with acute MA use followed by death due to acute drug intoxication or by the occurrence of hypersensitivity and reverse seen in cases of chronic drug abuse.

• Applied Biological Chemistry
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• 제32권4호
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• pp.350-356
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• 1989

무주산 오미자로부터 lignan 화합물인 deoxyschizandrin, gomisin N, schizandrin, gomisin A, wuweizisu C, angeloygomisin H 및 tigloylgomisin H를 분리 동정하고 capillary-GC (FID)를 이용하여 이들 화합물의 정량성을 조사하였다. 이 때 lignan 화합물의 동정에는 GC/MS (Finigan MAT 212; El, 70eV), 1H-NMR (Bruker FT; 300MHz) 및 IR (Perkin Elmer 599B)을 이용하였으며, lignan 화합물의 정량에는 FID 및 integrator(Hewlett-Packard 3393A)가 부착된 GC (Hewlett-Packard 5890A)를 이용하였다. 한편, GC column은 SPB-1 fused silica capillary$(0.25mm\;ID{\times}30m,\;Supelco)$를 사용하였고 column oven의 온도는 $200^{\circ}C$부터 $300^{\circ}C$까지 분당 $4^{\circ}C$씩 승온하였으며, carrier gas는 $N_2$, 1.0ml/min(split ratio=40 : 1)을 사용하였다. 각 lignan 화합물의 정량 가능농도범위는 deoxyschizandrin과 wuweizisu C가 $2{\sim}500ppm$이었고 gomisin N, schizandrin, gomisin A, angeloylgomisin H 및 tigloygomisin H 가 $5{\sim}500ppm$이었으며 무주산 오미자의 lignan성분 함량은 schizandrin이 6.50mg/g으로 가장 높았고 gomisin N, gomisin A, wuweizisu C, angeloylgomisin H, deoxyschizandrin, tigloylgomisin H의 순으로 낮은 경향이었다.

• Natural Product Sciences
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• 제26권1호
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• pp.97-107
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• 2020

Isolation of oils from leaves of Juniperus phoenicea and Juniperus oxycedrus was obtained by steam distillation extraction method. The compositions of essential oils (EOs) were studied by means of GC-MS and GC-FID, using the internal standard method and relative response factors. Around ninety eight compounds were determined in total, representing 98.25 g/100 g of EO of J. phoenicea and 98.48 g/100 g of EO of J. oxycedrus, respectively. The volatile leaf oils were dominated by the terpenic hydrocarbon fractions (79.87 g/100 g) and (61.27 g/100 g) characterized by high contents of α-pinene (64.6 g/100 g) and (54.0 g/100 g) in J. phoenicea and J. oxycedrus, respectively, as the main component. Also, the enantiomeric distribution of α-pinene, sabinene, camphene, δ-3-carene, β-pinene, limonene, linalool, terpinen-4-ol, bornyl acetate, and borneol in both oils is presented for the first time.