• Journal of Microbiology
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• 제35권3호
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• pp.193-199
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• 1997

From several industrial wastewaters, 14 bacterial strains which degrade benzene, toluene, o-xylene, m-xylene, or p-xylene (BTX) were obtained. These strains were characterized as to their species composition and the substrate range, kinetic parameters and the substrate interactions were investigated. Although BTX components have a similar chemical structure, isolated strains showed different substrate ranges and kinetic parameters. None of the strains could degrade all of BTX components and most of them showed an inhibition (Haldane) kinetics on BTX, BTX mixtures were removed under inhibitory substrate interactions with variation in the intensity of inhibition. For a complete degradation of BTX, a defined mixed culture containing three different types of patyways was constructed and all of the BTX components were simultaneously degraded with the totla removal rate of 225.69 mg/g biomass/h Judging from the results, the obtained mixed culture seems to be useful for the treatment of BTX-contaminated wastewater or groundwater as well as for the removal of BTX from the contaminated air stream.

• 한국산업보건학회지
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• 제7권2호
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• pp.245-263
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• 1997

For twelve solvent thinners, evaporation rates of components were investigated and models to estimate the actual concentration have been evaluated. Also, the current ACGIH TLVs (Threshold Limit Values) for the concentration of organic mixtures have been adjusted. The results of this study are summarized as follows : 1. Airborne concentrations of solvent thinner components were related to their respective vapor pressure (r=0.96). On the other hand, there was no significant relation between the concentrations in the air of the thinner compounds and the original amount in liquid form. 2. Airborne concentrations of each chemical were estimated by temperature at $8.5{\pm}1$, $16.7{\pm}1$ and $31.5{\pm}2^{\circ}C$ with an air velocity of 1.5 m/s. The concentrations were increased by increasing temperature (p<0.05). The percentage of concentrations were proportionate to their respective percentage of vapor pressure. Among the chemicals studied, n-butyl acetate, n-butyl alcohol, m-xylene, p-xylene and o-xylene showed a clear relationship to temperature. 3. Airborne concentration of each chemical was estimated by air velocity at 0.05, 1.50 and 2.50 m/s, with a constant temperature at $17{\pm}2^{\circ}C$. The concentrations were increased by increasing air velocity (p<0.05). The percentage of concentrations were proportionate to their respective percentage of vapor pressure. Among the chemicals studied, n-butyl alcohol, m-xylene and p-xylene showed a clear relationship to velocity. 4. In estimating the concentrations of solvent thinners by temperature and air velocity, ACGIH TLVs for mixtures tended to be larger than the values obtained by ACGIH exposure index. It shows that ACGIH TLVs for mixtures are not adequate for evaluating the airborne concentration of thinners and other organic mixtures. 5. The evaporation rate of the thinners were compared to the theoretical equations of Hummel, Braun and Mackay. The Hummel and Braun methods were close to exposure index but Makay's showed an underestimated value. In order to see the accuracy of each three models, the SSE (Error Sum of Squares) calculated for Hummel's was 1.73, being the closest to the actual values. 6. Present ACGIH TLVs for mixtures are not appropriate evaluate industrial environments. In this study, a correction of TLVs using vapor pressure of respective components was suggested. In order to evaluate the corrected TLVs a paired t-test was performed. There was no significant difference between the exposure index and the concentration over suggested TLVs (p>0.05). Thus, this corrected TLVs seem appropriate in order to evaluate actual industrial workplaces organic chemical concentration in the air.

• 한국지하수토양환경학회지:지하수토양환경
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• 제12권6호
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• pp.53-59
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• 2007

액체섬광계수기(liquid scintillation counter: LSC)를 이용한 지하수 $^{14}C$의 측정에서 휘발성유기화합물(volatile organic compounds: VOC)에 따라 소광효과(quenching effect)를 정확하게 보정할 수 있는 최적 소광곡선(quenching curve)의 작성조건을 조사하였다. 우선, VOC에 따른 소광효과를 알기 위하여 benzene, toluene, ethylbenzene, o-(m-,p-)xylenes, trichloroethylene(TCE)과 tetrachloroethylene(PCE), carbon tetrachloride, chloroform과 같은 주요 지하수오염유기물에 의한 소광인자(spectral quench parameter of the external standard, SQP(E))를 측정하였다. 소광곡선은 $^{14}C$ 표준용액과 chloroform 소광시약을 이용하여 작성하였으며 $^{14}C$ 표준용액의 비방사능(specific activity, dpm/mL), LSC 측정시간, 소광시약 농도 등의 최적조건을 도출하였다. 소광효과는 분자 내에 염소원자를 포함하지 않는 BTEX(benzene, toluene, ethylbenzene, o-(m-,p-)xylenes) 보다 염소원자를 포함하는 TCE, PCE, carbon tetrachloride와 chloroform에서 매우 높게 나타났다. 실험에서는 여건상 $^{14}C$ 비방사능이 7,000 dpm/mL 정도의 표준용액을 사용하였는데 이 경우 LSC측정시간은 100분, 소광시약으로 chloroform을 사용할 경우 수 mL의 첨가량이 적당하였다. 이러한 조건으로 BTEX(benzene, toluene, ethylbenzene, m-xylene)에 대해 작성한 소광곡선의 상관계수(coefficient of correlation)는 0.99이상으로 통계학적으로 신뢰할 수 있는 값을 얻을 수 있었으며 이 소광곡선을 지하수와 수돗물의 $^{14}C$ 측정에 적용한 결과 표준용액의 비방사능 값과 잘 일치하여 연구결과의 유효성을 확인할 수 있었다.

• Bulletin of the Korean Chemical Society
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• 제21권11호
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• pp.1101-1105
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• 2000

A simultaneous determination method of BTEX (benzene, toluene, ethylbenzene, o,m.p-xylene) and TPH (kerosene, diesel, jet fuel and bunker C) in soil with gas chromatography/flame ionization detection (GC-FID) was described. The effects of extracti on method, extraction solvent, solvent volume and extraction time on the extraction performance were studied. A sonication method was simpler and more efficient than Soxhlet or shaking methods. Sonication with 10 mL of acetone/methylene chloride (1 : 1, v/v) for 10 min was found to be optimal extraction conditions for 20 g of soil. Peak shapes and quantification of BTEX and TPH were excellent, with linear calibration curves over a wide range of 1-500 mg/L for BTEX and 10-5000 mg/L for TPH. Good reproducibilities by sonication were obtained, with the RSD values below 10%. By using about 20 g of soil, detection limits were 0.8 mg/L for BTEX and 10 mg/L for TPH. The advantages of this procedure are the use of simple and common equipment, reduced volumes of organic solvents, rapid extraction periods of less than 20 min, and simultaneous analysis of volatile and semivolatile compounds.

• 한국환경과학회지
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• 제21권1호
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• pp.11-21
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• 2012

This study investigated the characteristics of selected volatile organic compounds(VOCs) in newly-finished residential buildings, before the occupants moved in. This investigation was carried out by measuring the indoor and outdoor concentrations of selected VOCs before the occupants moved in and by utilizing an indoor mass balance model. Among 25 target VOCs, five aromatics(benzene, ethyl benzene, toluene, m,p-xylene, and o-xylene) were detected in all samples of both indoor and outdoor air. Toluene was most abundant VOC in the indoor air of new apartments, with a median value of 168 mg $m^{-3}$. Unlike other VOCs, halogenated compounds would not be significantly emitted from building materials. The indoor air concentrations of all selected VOCs, except for 1,3,5-trimethyl benzene, exhibited significant correlations each other, while for outdoor air concentrations, five aromatics only were significantly correlated between them. The emission rate of toluene was higher for the current study(median value, 76.8 mg $m^{-2}\;h^{-1}$) than for a previous study, while the emission rates of limonene, a-pinene and b-pinene(geometric means of 2.4, 13.8 and 9.6 mg $m^{-2}\;h^{-1}$, respectively) were lower and the emission rates of m,p-xylene and 2-butanone(geometric means of 10.9 and 21.3 mg $m^{-2}\;h^{-1}$, respectively) were similar. Although there were a few exceptions, the emission strengths are likely proportional to indoor temperature, and appear to reversely proportional to air exchange rate.

• Bulletin of the Korean Chemical Society
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• 제27권11호
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• pp.1757-1762
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• 2006

A solvent sublation using salphen as a ligand was studied and applied for the determination of trace Ni(II), Co(II) and Cu(II) in water samples. The fundamental study was investigated by a solvent extraction process because the solvent sublation was done by extracting the floated analytes into an organic solvent from the aqueous solution. The salphen complexes of Ni(II), Co(II) and Cu(II) ions were formed in an alkaline solution of more than pH 8 and then they were extracted into m-xylene. It was known that the each metallic ion formed 1 : 1 complex with the salphen and the logarithmic values of extraction constants for the complexes were 3.3 5.1 as an average value. Based on the preliminary study, the procedure was fixed for the separation and concentration of the analytes in samples. Various conditions such as the pH of solutions, the influence of $NaClO_4$, the bubbling rate and time of $N_2$ gas, and the type of organic solvent were optimized. The metal-salphen complexes could be extracted into m-xylene from the solution of more than pH 8, but the pH could be shifted to acidic solution of pH 6 by the addition of $NaClO_4$. In addition, the solvent sublation efficiency of the analytes was increased by adding $NaClO_4$. The recovery of 97-115% was obtained in the spiked samples in which given amounts of 0.3 mg/L Ni(II), 0.8 mg/L Co(II) and 0.04 mg/L Cu(II) were added.

• 한국산업보건학회지
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• 제3권2호
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• pp.177-187
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• 1993

The exposure levels of mixed organic solvents for 66 exposed workers in six paint manufacturing plants were evaluated. In 66 exposed workers and 30 control subjects, we also determined the concentrations of toluene and xylene metabolites, hippuric acid, ($o^-$, $m^-$, and $p^-$)methylhippuric acid. The results were as follow ; 1. Seven organic compounds, which on averge accounted for approximately 90% of the identified mass in each painting plants air samples, were selected for quantification : methyl ethyl ketone, ethyl acetate, methyl isobutyl ketone, toluene, butyl acetate, ethyl benzene, ($o^-$, $m^-$, $p^-$)xylene. 2. The average mixed organic solvent exposure levels in 66 points with workplce were 3.8ppm of MEK, 12.2ppm of ethyl acetate, 4.0ppm of MIBK, 28.7ppm of toluene, 3.8ppm of butyl acetate, 10.2ppm of ethyl benzene, 14.6ppm of xylene, respectively. 3. For the total 66 points with workplace, the rate of them of which mixed solvents in air was exceeded th TLV of 1.0 were obtained for 23%(15/66 point). 4. The concentrations of hippuric acid in urine of exposed group and control were $0.94{\pm}0.65g/g$ of creatinine, $0.16{\pm}0.11g/g$ of creatinine, respectively. 5. There was a linear correlation between the end shift hippuric acid acid levels in urine and exposed toluene in air : y=0.02079X+494.2, r=0.6488, n=55 y:hippuric acid in urine(mg/g of creatinine), x:toluene levels in air(ppb) Toluene levels of 100ppm in air have been caculated to hippuric acid of 2.57g/g of creatinine in urine. 6. There was a linear correlation between the end shift methylhippuric acid acid levels in urine and exposed xylene in air : y=0.01664X+31.6, r=0.7264, n=55 y:methylhippuric acid in urine(mg/g of crea.), x:xylene levels in air(ppb) Xylene levels of 100ppm in air have been caculated to methylhippuric acid of 1.69g/g of creatinine in urine.

• 한국환경과학회지
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• 제17권7호
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• pp.767-774
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• 2008

This study was carried out to evaluate the characteristics of atmospheric concentrations of volatile organic compounds(VOCs) and aldehydes for near a large shipyard. Most of the painting work in marine coating is performed indoor and outdoor. Most of the VOCs are emitted to the atmosphere as the paint is applied and cures. The massive scale of a ship makes it difficult to capture the emissions from outdoor painting. The VOCs are an important health and contributors to photochemical smog. The VOCs and aldehydes samples were collected using adsorbent tube and 2,4-DNPH cartridge, and were determined by an automatic thermal desorption coupled with GC/MS and HPLC-UV analysis, respectively. A total of 16 aromatic VOCs and 12 aldehydes of environmental concern were determined. At indoor coating facilities, the most abundant compound among 16 target VOCs appeared to be m,p-xylene, being followed by o-xylene. But most of the aldehydes were extremely lower concentrations. The atmospheric concentration of VOCs, m,p-xylene concentrations were the highest and the mean value were outdoor workshop 11.323 ppb, residental area 5.134 ppb, and green area 2.137 ppb, respectively. However, the most aldehydes were extremely lower concentrations such as formaldehyde, acetaldehyde and non-detection such as iso-valeraldehyde, n-valeraldehyde and o-tolualdehyde.

• 생명과학회지
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• 제24권1호
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• pp.54-60
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• 2014

방향족 화합물은 독성 환경오염물질로 생태계와 인간의 건강에 해로운 영향을 미친다. 그중 chlorotoluene과 nitrotoluene 화합물은 수생생물에 독성을 나타내며 인간의 피부, 눈, 호흡기를 자극한다. 본 연구에서는 폐수의 chlorotoluene과 nitrotoluene 화합물을 저렴하고 간단하게 검출하고자 재조합 미생물 바이오센서를 개발하였다. BTEX (benzene, toluene, ethylbenzene, xylene) 분해 조절 유전자 xylR를 Po' (upstream activating sequences를 제거한 DmpR 조절단백질 promoter Po) 또는 Pu (XylR 고유의 프로모터)::lacZ 유전자(${\beta}$-galactosidase 유전자)의 upstream에 연결한 플라스미드를 제작한 후, E. coli $DH5{\alpha}$에 형질 전환하였다. 유도 화합물 존재 하에서, 아가로스에 고정된 이 재조합 바이오센서 세포는 유도 화합물에 의해 ${\beta}$-galactosidase를 발현하고 기질인 chlorophenol red ${\beta}$-D-galactopyranoside (CPRG)를 분해하여 1~2시간에 붉은색을 나타내었다. BTEX 화합물 중, 특이적으로 o-, m-, p-chlorotoluene ($0.1{\mu}M-100 mM$) 그리고 o-, m-, p-nitrotoluene (0.1 mM-100 mM)에서 높은 반응을 나타내었으며 Po'가 Pu보다 높은 반응성을 보여주었다. 아가로스에 고정된 바이오센서는 $4^{\circ}C$에서 21일간 보존 후에도 활성의 큰 변화 없이 안정하였으며, chlorotoluene과 nitrotoluene 화합물들로 spike된 전처리 하지 않은 폐수 시료 중에서도 좋은 반응을 보여 주어 폐수 중 chlorotoluene과 nitrotoluene 화합물의 간단한 초기 검출에 활용될 수 있음을 제시하였다.

• 대한약학회:학술대회논문집
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• 대한약학회 2001년도 Proceedings of the Pharmaceutical Society of Korea
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• pp.184.2-185
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• 2001