• 미생물학회지
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• 제39권4호
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• pp.267-271
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• 2003

Polycyclic aromatic hydrocarbons(PAHs)를 분해하는 Burkholderia sp. D5를 유류 오염 토양으로 분리하였고, PAHs의 분해특성을 조사하였다. 분리균주는 유일 탄소원으로 phenanthrene(Phe)을 이용하여 생장이 가능하였고, pyrene (Pyr)을 유일 탄소원으로 이용하여 생장하지는 못하였으나 yeast extract(YE)를 공기질로 첨가해 준 조건에서는 Pyr를 분해할 수 있었다. 분리 균주의 PAH 분해속도는 YE, peptone 및 glucose의 첨가에 의해 향상되었으며, 특히 YE 첨가 효과가 가장 우수하였다. 무기염배지(BSM)에 215 mg-Phe/L와 1 g-YE/L를 첨가한 조건에서 Burkholderia sp. D5의 비생장속도(0.28/h)와 Phe 분해속도(29.30 ${\mu}mol$/L/h)는 YE를 첨가하지 않은 조건에서 얻은 비생장속도(0.02/h)와 Phe 분해속도(12.00 ${\mu}mol$/L/h)의 각각 10배 및 2배였다. Phe를 기질로 공급한 경우 최대 비생장속도(${\mu}$_max)와 최대 Phe분해속도(V_max)는 각각 0.34 h-1 및 89 ${\mu}mol$/L/h 이었고. Pyr을 기질로 공급한 경우 ${\mu}$_max와 V_max는 각각 0.27 h-1 및 50 ${\mu}mol$/L/h이었다. Phe 혹은 Pyr 단독 기질하에서 분해속도와 비교 하였을 때(29.30 ${\mu}mol$-Phe L/h, 9.58 ${\mu}mol$-Pyr L/h), 두 기질의 혼합조건에서 Phe와 Pyr 분해속도는 각각 2.20 및 2.18 ${\mu}mol$ L/ h로 저하되었다. Burkholderia sp. D5 균주는 토양에서 Phe와 Pyr을 분해할 수 있었는데, Phe와 Pyr 분해속도는 각각 20.03 및 1.09 ${\mu}mol$ L/h 이었다.

• Journal of Microbiology and Biotechnology
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• 제24권9호
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• pp.1170-1177
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• 2014

Mycobacterium gilvum PYR-GCK is a bacterial strain under study for its bioremediation use on heavy hydrocarbon pollutants in the environment. During the course of our study, mammalian cell entry (mce) genes, known to facilitate pathogenicity in M. tuberculosis, were highly expressed during a comparative and substrate-related cultural global transcriptomic study. RNA sequencing of the global transcriptome of the test strain in two different substrates, pyrene and glucose, showed high expression of the mce genes based on the differential results. After validating the expression of these genes with quantitative real-time PCR, we arrived at the conclusion that the genes were expressed based on the pyrene substrate (a phytosterol compound), and sterol metabolism is said to activate the expression of the mce genes in some actinomycetes bacteria, M. gilvum PYR-GCK in this case. This study is believed to be important based on the fact that some mycobacterial strains are undergoing a continuous research as a result of their use in practical bioremediation of anthropogenic exposure of toxic organic wastes in the environment.

• 분석과학
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• 제17권1호
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• pp.45-52
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• 2004

현이차 미분 형광 분광광도법을 이용하여 울산만 해양 저질토양중의 PAHs를 n-hexane용매로 추출하여 11종의 PAHs를 동시 정량분석하였다. Acenaphthene (Ace), anthracene (Anth), benzo(a)pyrene (BaP), benz(a)anthracene (BaA), benzo(b)fluoranthene (BbFt), benzo(k)fluoranthene (BkFt), chrysene (Chry), perylene (Per), phenanthrene (Phen), pyrene (Pyr) 및 fluoranthrene (Ft) 등을 정량분석 하였다. 이들 성분들의 검정선은 대략 0.15~166 ppb의 농도범위에서 직선관계를 보였으며, 0.999이상의 좋은 직선 상관계수를 보였다. 울산만의 해양 저질 토양 (sediment)에 함유된 11종의 PAHs 총량은 68.8 ng/g ~ 324.4 ng/g의 농도범위로 함유되어 있었다. 또한 PAHs의 총량은 울산만의 안쪽으로 갈수록 증가하는 경향을 보였으며, 특히 Pyr과 BaA 등과 같은 4고리화합물의 함량비가 높았다.

• Korean Chemical Engineering Research
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• 제56권6호
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• pp.792-797
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• 2018

We have explained the synthesis of novel phenanthrene and pyrene substituted phthalocyanines (PC-PHE and PC-PYR) and fully confirmed the structures by its spectral, photo physical and elemental analysis. For these phthalocyanines we checked the UV-Visible absorbance in PGMEA and chloroform and transmittance checked in PGMEA. The transmittance results suggested that these phthalocyanines are showing more than 90% transmittance at the 450-550 nm region. These synthesized molecules are nicely soluble in almost all industrial solvents. We checked the aggregation property of these phthalocyanines in PGMEA, and the results suggested no any aggregation for these molecules in PGMEA. The thermogravimetric analysis results concluded that PC-PHE and PC-PYR had high thermal stability. All studies explain that these new phthalocyanines are more suitable for LCD green color filter application.

• 한국지하수토양환경학회지:지하수토양환경
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• 제22권2호
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• pp.26-32
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• 2017

Regression analyses were conducted for prediction of benzo(a)pyrene (BaP) and total polycyclic aromatic hydrocarbons (PAHs) in soils. Dimensionless units were applied after each PAH was divided by naphthalene (Nap) for the regression analyses using a previously published Swiss data set or all data sets, including Chinese and Brazilian. A strong correlation was found between BaP/Nap ($R^2=0.95$) or ${\Sigma}PAH/Nap$ ($R^2=0.99$) and Pyr/Nap ratios from the Swiss data set. When the developed prediction equation was applied to other measurements to validate its accuracy, there was great agreement between the data and predicted values. This model could be used as a useful tool for the calculation of average BaP and ΣPAH in specific regions without additional tests.

• 한국지하수토양환경학회지:지하수토양환경
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• 제27권6호
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• pp.11-21
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• 2022

Sorption of phenanthrene (PHE) and pyrene (PYR) in several sorbents, i.e., natural soil, BionSoil^®, Pahokee peat, vermicompost and Devonian Ohio Shale and a surfactant (hexadecyltrimethyl ammonium chloride)-modified montmorillonite (HDTMA-M) were investigated. Pyrene exhibited higher sorption tendency than phenanthrene, as predicted by its higher octanol to water partition coefficient (K_ow). Several sorption models: linear, Freundlich, solubility-normalized Freundlich model, and Polanyi-Manes model (PMM) were used to analyze sorption isotherms. Linear isotherms were observed for natural soil, BionSoil^®, Pahokee peat, vermicompost, while nonlinear Freundlich isotherms fitted for Ohio shale and HDTMA-M. The relationship between sorption model parameters, organic carbon content (f_oc), and elemental C/N ratio was studied. In the binary competitive sorption of phenanthrene and pyrene in natural soil, competition between the solutes caused reduction in the sorption of each solute compared with that in the single-solute system. The ideal adsorbed solution theory (IAST) coupled with the single-solute Freundlich model was not successful in describing the binary competitive sorption equilibria. This was due to the inherent nature of linear sorption of phenanthrene and pyrene in natural soil. The result indicates that the applicability of IAST for the prediction of binary competitive sorption is limited when the sorption isotherms are inherently linear.

• 한국환경과학회지
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• 제15권5호
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• pp.397-403
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• 2006

Compositional characteristics and origin of polycyclic aromatic hydrocarbons(PAHs), which should be strongly regulated for environmental protection in the crude oils and petroleum products, have been investigated by gas chromatography-mass spectrometry(GC/MS). In the crude oils analyzed, two-rings compound(naphthalene) of PAHs was detected around $72.3\sim93.5%$, but five- or six-rings compound of PAHs was not detected. In the crude oils analyzed, the molecular ratio indices of Phe/Ant(phenanthrene/anthracene)>15, Fla/Pyr(fluoranthene/pyrene)<1, BaA/Chr(benzo (a)anthracene/chrysene)$\leq0.4$ could be effectively applied, and we found that the origin of PAHs was petrogenic sources. Total PAHs concentrations in the crude oils were increased with increasing API gravity and with decreasing sulfur contents of the analyzed crude oils. Five- or six-rings compound of PAHs were not included in ail petroleum products except bunker-C. Furthermore, the molecular ratio indices of Phe/Ant(phenanthrene/anthracene) vs. Fla/Pyr(fluoranthene/pyrene) could be effectively applied as the standard for the PAHs contamination criterion at the other Korean areas.

• 한국대기환경학회지
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• 제20권1호
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• pp.129-138
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• 2004

Determination of some PAHs in ambient air at Ulsan have been carried out by collection of the components into n-hexane followed by synchronous spectrofluorimetric technique. 10 PAHs, such as acenaphthene (Ace), anthracene (Anth), benz[a]anthracene (BaA), benzo[b]fluoranthene (BbFt), benzo[k]fluoranthene (BkFt) benzo[a]pyrene (BaP), chrysene (Chry), phenanthrene (Phen), fluoranthene (Ft), perlyrene (Per), and pyrene (Pyr) in air samples were able to determine separately by synchronous spectrofluorimetry. Calibration curves for those components were linear for the concentration range of 0.2∼166ppb PAHs with the correlation factor of 0.9985∼0.9999. The predominant contribution was phenanthrene which was included 36.9∼85.1% to the overall level of the 10 PAHs in some areas. Also benzo[a]pyrene which was known to carcinogenicity was detected from 6.4 to 55.8ng/㎥, benzo[a]anthracene of some areas was contained from 21.9∼153ng/㎥.

• 분석과학
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• 제24권4호
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• pp.266-274
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• 2011

Hitachi LaChromUltra 2000U를 사용하여 역상의 초고속액체크로마토그래피 방법으로 식품 중의 PAHs 14종을 신속하게 분석하는 방법을 개발하였다. PAHs분석을 위한 방법은 solid phase extraction (SPE)법에 의한 정제 후 u-HPLC를 사용하여 형광검출기로 분석하였다. 이 분석법은 감도가 매우 좋았으며, 식품 중의 PAHs를 ${\mu}g$/kg수준에서 분석이 가능하였다. 6개의 시료를 분석한 결과 모든 시료에서 PHE가 검출되었고, 그 함량은 2.5~19.9 ${\mu}g$/kg이었다. Benzo[c]fluorine (BCL), pyrene (PYR), benzo[a]anthracene (BaA), chrysene (CHR), benzo[b]fluoranthene (BbF), benzo[k]fluoranthene (BkF) 이 ${\mu}g$/kg이하의 농도에서 검출되었으나 그 농도는 모두 정량한계 이하이었다.

• Environmental Engineering Research
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• 제20권2호
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• pp.149-154
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• 2015

In recent years, immobilization agents were introduced into organic contaminated soil remediation and more and more materials were screened and used as the immobilizing carrier. However, effect of the decomposition of the immobilizing carrier on the bioremediation was rarely concerned. Therefore, the decomposition experiment of immobilizing carrier -corncob was carried out in the lab with the efficient degradation fungi - Mucor mucedo (MU) existing, and polycyclic aromatic hydrocarbons (PAHs) residues E4/E6 of the dissolved organic matter and microbial diversity during the decomposition process were studied. The results showed that: a) during the decomposition, the degradation of pyrene (Pyr) was mainly in the first 28 d in which the content of extractable Pyr decreased rapidly and the highest decrease was in the treatment with only MU added. b) Anslysis of E4/E6 changes showed that rich microorganisms could promote aromatization and condensation of humus. c) From the diversity index analysis it can also be seen that there is no significant difference in effects of PAHs on the uniformity of microorganisms. These results will not only be useful to have a better understanding of the bioavailability of contaminants adsorbed to biodegradable carriers in PAHs contaminated soil remediation, but also be helpful to perfect the principle of immobilized microbial technique.