• Journal of Environmental Health Sciences
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• v.44 no.2
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• pp.160-168
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• 2018

Objectives: The purposes of the study were to investigate hazardous pollutant emissions changes among group 1 carcinogens. The emissions characteristics were compared with national cancer registration statistics. Methods: A survey of group 1 carcinogen hazardous pollutant emissions (trichloroethylene, benzene, vinyl chloride, formaldehyde, 1,3-butadiene, ethylene oxide, chromium and its compounds, 3,3'-dichloro-4,4-diaminodiphenylmethane, chloromethyl methyl ether, arsenic and its compounds, cadmium and its compounds, o-toluidine) was conducted through a homepage for 2001-2015. The emission of hazardous chemicals and the cancer trend analysis for 2001-2015 were performed using the Korean statistical information service through its homepage as a reference. Results: Emissions of more than 95% of the substances listed as group 1 carcinogens over the last five years were made up of trichloroethylene, benzene, vinyl chloride, formaldehyde, 1,3-butadiene, and ethylene oxide. As a result of the comparison of emission results and cancer incidence rates, carcinogen pollutant emissions showed a tendency to decrease continuously. In addition, the incidence of cancer tended to increase, but showed a tendency to decrease from 2012. Conclusion: The results indicate hazardous pollutant emissions have continued to increase. However, no association between emissions and health effects was shown and more research is needed.

• Molecular & Cellular Toxicology
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• v.4 no.1
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• pp.45-51
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• 2008

Volatile Organic Compounds (VOCs) have been shown to cause nervous system disorders through skin contact or respiration, and also cause foul odors even at low densities in most cases. Also, as a compound itself, VOCs are directly harmful to the environment and to the human body, and may participate in photochemical reactions in air to create secondary pollutants. In this study, HL-60 cells were treated with volatile organic compounds, including ethylbenzene and trichloroethylene, at a value of $IC_50$. Then, the in house-prepared Human HazChem arrayer was utilized in order to compare the gene expression between the two VOCs. After hybridization, 8 upregulated genes and 8 downregulated genes were discovered in the HazChem array. The upregulated genes were identified as SG15, TNFSF10, PRNP, ME1, NCOA4, SRXN1, TXNRD1, and XBP1. The downregulated genes were identified as MME, NRF1, PRARBP, CALCA, CRP, BAX, C7 or f40, and FGFR1. Such results were highly correlated with the quantitative RT-PCR results. The majority of the 16 genes were related with the characteristics of VOCs, including respiratory mechanism, apoptosis, and carcinogenesis-associated genes. Our data showed that our human HazChem array can be used to monitor hazardous materials via gene expression profiling.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2002.04a
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• pp.191-194
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• 2002

토양증기추출(Soil Vapor Extraction)법을 이용하여 대표적 휘발성 NAPL (Non-aqueous phase liquid)인 TCE (trichloroethylene)와 toluene을 토양으로부터 제거하는 칼럼 실험을 실시하였다. 토양특성 및 증기추출 조건들이 정화효율에 미치는 영향을 규명하는데, 균질한 Ottawa sand와 실제 오염지역의 토양들을 직경 2.5cm, 길이 30cm인 유리 칼럼이 충진시켰으며, 빨갛게 염색된 TCE 또는 toluene 4 g이 주입되었다 공기 유량계를 설치하여 0.03L/min의 일정한 속도로 공기가 주입되도록 하고, 퍼지장치를 설치하여 주입 공기의 습윤도를 99% 이상으로 유지하였다. 가스크로마토그래피로 유출 가스 농도를 분석하였다. Ottawa sand로 충진된 칼럼실험에서는 매질의 입자크기, 함수율, 토양 내 오염물 체류시간 등을 변화시켜 실험을 반복하였다. TCE로 오염된 세립질 Ottawa sand 칼럼실험에서 유출 공기의 최대 농도는 조립질 Ottawa sand 칼럼의 유출 농도보다 약 20% 정도 감소하였고, 오염지역의 실제토양 칼럼실험에서는 최대유출농도가 조립질 Ottawa sand 칼럼의 농도보다 약 50% 감소하였으나, 20 liter공기 주입 후부터는 모두 비슷한 농도감소 현상을 나타내었으며, 초기 주입량의 90 % 이상이 제거되었다. 함수율증가에 따른 유출공기의 농도 감소는 거의 나타나지 않았으며, TCE 주입 후 7일 동안 방치하였다가 SVE를 실시한 칼럼 실험에서도 잔류하는 TCE의 양이 약간 증가하였지만 20 liter 공기 추출 후에는 초기 주입량의 90% 가, 40 liter공기 추출 후에는 98% 이상이 제거되었다. Toluene으로 오염된 칼럼 실험에서도 TCE와 비슷한 제거 경향을 나타냈으며 200 liter 공기 추출 후에는 오염물 초기 주입량의 98% 이상이 제거되었다. 본 실험 결과로부터 증기추출법을 이용한 TCE, toluene 정화 효율성이 규명되었으며, 휘발성 NAPL로 오염된 실제 토양을 복원하기 위한 SVE법의 적용가능성을 확인할 수 있었다.

• Journal of Korean Society on Water Environment
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• v.29 no.4
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• pp.489-496
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• 2013

Ground water underlying soil is vulnerable to pollution by organic chemicals through their percolation through the soil system. This study was conducted to provide information on the seepage behavior of organic chemical contaminants in clay, silty and sandy soils. Chloroform, 1,1,1-trichloroethane and trichloroethylene are readily transported through the soil; their percolated mass were 4.6-19.2 percent of the total mass applied. Tetrachloroethylene, 1,2-dichlorobenzene and 1,3-dichlorobenzene were retarded by soils due to sorption. Between 0.6 and 4.8 percent of the material applied to the surface percolated within the experimental period. Carbon tetrachloride was attenuated considerably by passage through soils. Only 0.1-0.4 percent of the mass reached the groundwater. Significant degradation of bromoform was observed. Apparent breakdown of intermediates of the brominated compounds were detected. Transformations of the brominated compounds appear to be the result of both biological and chemical processes. The effect of soil type on the mobility of organic chemical contaminants was considerable. The organic contaminants moved faster in sandy soil than in either clay or silty soils.

• Korean Journal of Environmental Biology
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• v.17 no.4
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• pp.513-519
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• 1999

Volatile organic compounds (VOCs) were analyzed on the seawater from 17 stations in Kwangyang Bay throughtout the year. We could not detect 10 VOCs; methylene chloride, tetrachloromethane, 1, 1, 1-trichloroethane, trichloroethane, 1, 1, 1, 2-tetrachloroethane, trichloroethylene, bromoethane, dibromoethane, bromobenzene, 1-ethyl-3-methylbenzene. The other VOCs-chloroform, 1, 2-dichloroethane, ethylbenzene, benzene, toluene, m, p-xylene, methylethylketone, styrene, hexane-were detected with a little variance according to the sampling stations and the sampling seasons. The concentrations of chloroform (0.6 ~ 49.9 $\mu$g/1) and toluene (0.42 ~ 48.3 $\mu$g/1) were high and they were detected more frequently than the other detected VOCs. We also tried to seek the correlation between the physicochemical environmental factors and VOCs. Only toluene had the high correlation coefficient with the water temperature (r = -0.524) and with the pH (r = 0.319). Correlation between VOCs themselves showed some interesting results. The benzene had high correlation coefficient (r = 0.549 ~ 0.662) with three VOCs such as toluene, m, p-xylene, ethylbenzene. From these results it is suggested that VOCs might be discharged simultaneously in Kwangyang Bay.

• Journal of Environmental Science International
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• v.23 no.5
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• pp.829-837
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• 2014

Titania-supported chromium oxides with different loadings have been embarked in catalytic oxidation of trichloroethylene (TCE) to inquire association of the formation of crystalline $Cr_2O_3$ with catalytic performances. A better activity in the oxidative TCE decomposition at chosen temperatures was represented when chromium oxides ($CrO_x$) had been dispersed on pure anatase-type $TiO_2$ (DT51D) rather than on phase-mixed and sulfur-contained ones such as P25 and DT51. The extent of TCE oxidation at temperatures below $350^{\circ}C$ was a strong function of $CrO_x$ content in $CrO_x$/DT51D $TiO_2$, and a noticeable point was that the catalyst has two optimal $CrO_x$ loadings in which the lowest $T_{50}$ and $T_{90}$ values were measured for the TCE oxidation. This behavior in the activity with respect to $CrO_x$ amounts could be associated with the formation of crystalline $Cr_2O_3$ on the support surface, that is less active for the oxidation reaction, and an easier mobility of the surface oxygen existing in noncrystalline $CrO_x$ species with higher oxidation states, such as $Cr_2O_8$ and $CrO_3$.

• Journal of Korean Society of Occupational and Environmental Hygiene
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• v.6 no.1
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• pp.109-124
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• 1996

This study was performed to evaluate the performance of three passive samplers made in U.S.A. Three passive samplers selected for this study included products made by 3M, Gilian, and SKC in U.S.A. Three organic solvents, such as toluene, trichloroethylene, and n-hexane which are used frequently in Korean industry were selected for the study. Conclusions obtained from this study are summarized as follows. 1. For toluene and trichloroethylene, the overall accuracy of the results from all of three products was within 25 %, which is the criteria recommended by the U.S. National Institute for Occupational Safety and Health (NIOSH). For n-hexane, the overall accuracy of the results from two products except 3M was exceeding 25 %. Thus 3M product showed the best accuracy among three products. 2. When passive samplers collected organic vapors were exposed to clean air for two hours, there were 12 - 16 % loss of organic vapors due to reverse diffusion in Gilian products. There was no significant loss in results from other two products. 3. Air velocity affected greatly on the performance of passive samplers which did not have permeation membrane. At high velocity, 100 cm/sec, accuracies of results from Gilian and SKC were 57 - 108 and 128 - 164 %, respectively. However, the results from 3M samplers, which contain permeation membrane, indicated accuracy below 25 %. 4. When passive samplers collected organic vapors for eight hours, the accuracy was reduced. Thus, it is recommended that passive samplers be used for less than four hours.

• Journal of Soil and Groundwater Environment
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• v.21 no.6
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• pp.192-203
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• 2016

A field investigation was conducted on an aquifer contaminated with trichloroethylene (TCE) for application of in situ reactive zone treatment using nanosized zero-valent iron (NZVI). The aquifer was an unconfined aquifer with a mean hydraulic conductivity of $5.14{\times}10^{-4}cm/sec$, which would be favorable for NZVI injection. Seasonal monitoring of TCE concentration revealed a presence of non-aqueous phase liquid form of TCE near IW (injection well). The hydrochemical data characterized the site groundwater to be a $Ca-HCO_3$ type. The average value of Langelier Saturation Index of the groundwater was -1.33, which implied that the site was favorable for corrosion of NZVI. Dissolved oxygen (DO) concentration varied between 2.5~11.5 mg/L, which indicated that DO would greatly compete with TCE as an electron acceptor. The hydrogeological and hydrochemical characterization reveals that the time around November would be appropriate for NZVI injection when water level and temperature are relatively high and DO concentration is low.

• Journal of the Korea Organic Resources Recycling Association
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• v.16 no.1
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• pp.46-52
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• 2008

Oils and chlorinated solvents leaking to the subsurface are entrapped in the soil pore and these are called as nonaqueous phase liquids (NAPL). NAPL entrapped in porous media acts as a continuous source for surface and ground water contamination. This study visualized dissolution of trichloroethylene (TCE) entrapped in porous media and quantified the velocity of TCE dissolution using an image analysis technique. As the water velocity increased, the level of dissolution increased. The results imply that a TCE contaminated region having a high infiltration rate and groundwater velocity may result in severe groundwater contamination. Microscopic images of TCE entrapped in porous media showed that TCE present in the preferential flow paths was easily dissoluted into the water phase. However, TCE present in the stagnant flow region was visualized for long time. The results imply that TCE would be still present in the soil if TCE is detected in goundwater.

• Journal of Korean Society of Environmental Engineers
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• v.31 no.6
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• pp.419-427
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• 2009

To test applicability for continuous flow treatment of ultrasound technology, sonolysis of TCE aqueous solution using 584 kHz multi irradiation reactor was performed under batch and continuous flow conditions. Under batch condition (3 and 4 sides irradiation, 600 W), first order degradation rate constant of TCE was higher under 4 sides than 3 sides irradiation conditions, while the generation of $H_2O_2$ and chloride was similar under both irradiation conditions. Under continuous flow condition with 4 sides irradiation, removal efficiencies of TCE in steady-state were decreased from 83 to 48% with increasing flow rate from 67 to 300 mL/min at 600 W, and were increased from 14 to 75% with increasing acoustic power from 100 to 600 W at 100 mL/min. Removal efficiency of TCE in groundwater was decreased 10% compared to in distilled water at 100 mL/min and 600 W.