• Korean Journal of Microbiology
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• v.30 no.5
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• pp.366-370
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• 1992

Sediment samples were collected from the stations 0101-0921 located between N $32^{\circ}$30'~$34^{\circ}$30' and E $123^{\circ}$30'-$128^{\circ}$30' during July 31-August lO. 1988. The distributions of total heterotrophic bacteria, freshwater bacteria and hydrocarbon degrading bacteria were studied. Each bacterial distribution was in the range of $3{\times}10^{5}~9.2{\times}10^{6}CFU/cm^{3}$sediment, $3{\times}10^{3}~2.1{\times}10^{6}CFU/cm^{3}$ sediment and $2{\times}10^{4}~6.2{\times}10^{6}CFU/cm^{3}$ sediment. respectively. The percent of hydrocarbon degrading bacteria against total heterotrophic bacteria was 0.7-73,2 % which was much higher than other marine sediments reported. These values were statistically analyzed with the percent of freshwater bacteria against total heterotrophic bacteria. These two parameters were well correlated with the correlation coefficient r= 0.60058 (n=34) and P=0.OOO2. This means that the distributions of hydrocarbon degrading bacteria and freshwater bacteria in the research area were affected together by the fresh water discharge into the sea environment. Therefore it can be concluded that the distribution of hydrocarbon degrading bacteria in the sediment of South Sea was affected by petroleum hydrocarbon input from terrestrial region through rivers.

• Proceedings of the Korea Air Pollution Research Association Conference
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• 2002.11a
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• pp.417-418
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• 2002

열분해는 독성이 강한 염화탄화수소의 처리뿐만 아니라 염화물을 효과적으로 제거하여 이들로부터 유용한 탄화수소를 얻을 수 있는 반응이다 Biomass에 열분해를 적용하여 가스상, 액상, 고상형태의 유동한 부산물로 전환시키고 있으며 현재 액상생성물은 외국에서 큰 주목을 받고 있는 부산물이다. 1,1,2-trichloroethane(TCE)는 독성이 강한 휘발성 유기화합물(VOC)이며 발암물질이다. (중략)

• Proceedings of the Korea Air Pollution Research Association Conference
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• 2003.05b
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• pp.271-272
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• 2003

다환방향족 탄화수소(PAHs)는 도시 대기입자상물질 중에 광범위하게 존재하고 있으며 그들의 발암성 및 변이성으로 인하여 건강과 관련하여 많은 주목을 받고 있다(Kado et at., 1996; Nielsen et al., 1996; Kao, 1994; Manzie et al., 1994). 다환방향족 탄화수소는 탄소나 수소를 함유한 유기물질의 불완전연소나 열분해에 의해서 생성된다. 연소과정에서 배출되는 다환방향족 탄화수소는 배출원에서 초기에 가스상태로 배출되나 상당량은 대기중의 입자상물질에 흡착된다. 산불이나 화산 등에서도 다환방향족 탄화수소에 기여하나 대기로 유입되는 대부분은 인위적인 배출원에서 배출된다. (중략)

• Applied Chemistry for Engineering
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• v.18 no.1
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• pp.84-89
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• 2007

Direct decomposition of hydrocarbon (methane, propane) was studied using a thermal plasma to produce high purity hydrogen and carbon black. Thermodynamic equilibrium compositions were calculated based on the minimization of Gibb's free energy, and decomposition experiments were performed on the basis of calculation results. The purity of hydrogen was found to be depended strongly on the flow rate of hydrocarbon. The decomposition conditions for high purity hydrogen were investigated. The purity of hydrogen produced from methane decomposition was higher than that from propane. In the case of propane, it was investigated that by products such as methane, acetylene, and ethane etc., by radical recombination under thermal plasma were produced more than that of methane. Produced carbon blacks were characterized by material analyses, such as XRD, Raman spectroscopy, SEM, and particle size analysis. In both methane and propane decompositions, well-crystallized carbon blacks were produced and showed uniform and sphere-like morphologies. The size of carbon black synthesized from methane was observed to be smaller than that from propane.

• Economic and Environmental Geology
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• v.37 no.6 s.169
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• pp.613-629
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• 2004

Contamination of groundwater by volatile organic compounds (VOCs) was investigated for 168 groundwater wells in Ulsan area to study the natural attenuation of organic compounds in the aquifers. As groundwater contamination by VOCs is closely related to land use, 168 groundwater samples were classified into 4 different groups; agricultural, forestry, industrial, and residential & business. From analysis 65 out of 168 groundwater samples contained more than one VOC. Analysis of samples were performed fir 36 halogenated aliphatic hydrocarbons and 25 petroleum hydrocarbons set up by NAWQA of US geological survey. Twelve petroleum hydrocarbons were detected in 26 groundwater wells, but their concentrations were less than 1.5 g/L except for MTBE. Twenty three chlorinated aliphatic hydrocarbons, composed of 11 methanes, 6 ethanes and 6 ethenes, were detected in 63 groundwater samples. The range of methanes concentration was $ND\~330\;/gL,\;ethanes\;ND\~84\;gL$, and PCE and their derivatives $ND\~62\;g/L$. As the study area was comprised of the aerobic/denitrification zones and $Fe^{+3}$ redox condition, most of petroleum hydrocarbons were degraded well, while halogenated hydrocarbons were slowly biodegradation.

• Clean Technology
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• v.28 no.4
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• pp.331-338
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• 2022

The objective of this study is to prepare bead-type and pellet-type Pt (1 wt%)/Kieselguhr catalysts as hydrogenation catalysts for the polycyclic aromatic hydrocarbons (PAHs) included in pyrolysis fuel oil (PFO). The optimal reaction temperature to maximize the yield of saturated cyclic hydrocarbons during the PFO-cut hydrogenation reaction in a trickle bed reactor was determined to be 250 ℃. A hydrogen/PFO-cut flow rate ratio of 1800 was found to maximize 1-ring saturated cyclic compounds. The yield of saturated cyclic compound increased as the space velocity (LHSV) of PFO-cut decreased. The difference in hydrogenation reaction performance between the pellet catalyst and the bead catalyst was negligible. However, the catalyst impregnated by Pt after molding the Kieselguhr support (AI catalyst) showed higher hydrogenation activity than the catalyst molded after Pt impregnation on the Kieselguhr powder (BI catalyst), which was a common phenomenon in both the pellet catalysts and bead catalysts. This may be due to a higher number of active sites over the AI catalyst compared to the BI catalyst. It was confirmed that the pellet catalyst prepared by the AI method had the best reaction activity of the prepared catalysts in this study. The majority of the PFO-cut hydrogenation products were cyclic hydrocarbons ranging from C₈ to C₁₅, and C₁₁ cyclic hydrocarbons had the highest distribution. It was confirmed that both a cracking reaction and hydrogenation occurred, which shifted the carbon number distribution towards light hydrocarbons.

• KSBB Journal
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• v.18 no.6
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• pp.529-535
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• 2003

We studied degradation effects of hydrophobic substrate such as kerosene and diesel by adding a biosurfactant originated from Pseudomonas aeruginosa F722 and chemical surfactants (Tween 80 and detergent) with aeration. The surface tensions of the biosurfactant, Tween 80 and detergent were 30mN/m, 39mN/m and 31mN/m, respectively. When the concentration of biosurfactant added in C-medium was 0.01 and 0.15%(w/v), the ratios of hydrocarbon degradation were 94.3％ and 94.2% respectively. It was 6.2%(w/v) higher than when the concentrations of added biosurfactant were 0.05, 0.1 and 0.2％. The degradation ratios of the chemical surfactants (Tween 80 and detergent) were 94.5％ and 93.5％ respectively. The effects of the biosurfactant and chemical surfactants were similar on the degradation ratio in mixtures of kerosene and diesel. However, the population of viable p. aeruginosa F722 at the end of the cultivation period was twice as higher in the biosurfactant than that in the chemical surfactant. We also studied the effect of aeration (0.5vvm) on the degradation ratio. The biosurfactant addition experiment was conducted with 0.5vvm air, 35$^{\circ}C$, 150rpm, pH 8.0, 3days, 1.0% (w/v) substrate. When p. aeruginosa F722 and 0.15%(w/v) biosurfactant were added, the degradation ratio of hydrocarbon was 94.8％. Without p. aeruginosa F722, it was 68%. Thus, with aeration, the degradation ratio of hydrocarbon was increased by 26.8％. In addition, the cultivation time was shortened by 1/3. The degradation ratios of hydrocarbon in shaking culture (cultivation time; 3days) and stationary culture (cultivation time; 10days) were 94.8 and 93.7％ respectively. Thus, the addition of biosurfactant and aeration enhanced the degradation of hydrocarbon originated kerosene and diesel.

• Korean Journal of Environmental Biology
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• v.18 no.3
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• pp.307-313
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• 2000

Aromatic hydrocarbons are known to be recalcitrant, so that they have been concerned as pollutant chemicals. Microorganisms play a major role in the breakdown and mineralization of these compounds. However, the kinetics of the biodegradation process may be much slower than desired from environmental consideration. The biodegradation of aromatic hydrocarbons is conducted by oxidation to produce catechol as a common intermediate which is metabolized for carbon and energy sources. In this study, a bacterial isolate capable of degrading several aromatic hydrocarbons was isolated from the contaminated wastewater of Yeocheon industrial complex. On the basis of biochemical characteristics and major cellular fatty acids, the isolate was identified as Pseudomonas putida Z104. The strain Z104 can utilize benzoate and catechol as the sole carbon and energy sources via a serial degradative pathway. The strain degraded actively 0.5 mM catechol in MM2 medium at pH 7.0 and 3$0^{\circ}C$.

• 한국신재생에너지학회:학술대회논문집
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• 2005.11a
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• pp.638-641
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• 2005

수소는 자원이 무한하고 청결한 에너지이다. 수소는 무공해 청정 대체연료로 사용될 수 있을 뿐만 아니라 풍부한 자원으로부터 얻을 수 있다. 수소에너지는 물을 분해하여 얻거나 화석연료를 수증기개질 또는 부분산화 시킴으로써 얻을 수가 있다. 수소에너지는 1차 에너지를 변환시켜 얻을 수 있는 2차 에너지로서 환경에 대한 부하가 거의 없어 향후 화석연료를 대체할 수 있는 가장 가능성이 높은 에너지이며, 연료전지의 상용화를 앞두고 있어 중요성이 더욱 증대되고 있다. 수소를 생산하는 방법 중 가장 이상적인 방법으로는 물분해함으로써 수소를 제조하는 방법이 있다. 그러나 물분해에 의한 수소생산은 제조비용이 비싸 경제성이 떨어진다는 점과 수소의 대량생산에 필요한 기술확보가 여의치 않아 어렵다. 그러므로 수소를 저 비용으로 대량 생산할 수 있는 수소 제조 기술의 확보가 선행되어야 할 것이다. 현재 상용화되어 있는 수소제조방법은 거의 석유나 천연가스의 수증기 개질에 의한 수소 제조 방법이다. 그러나 이러한 방법은 유해 환경 물질인 CO나 $CO_2$를 배출하는 단점을 지니고 있다. 이러한 단점을 보완키 위한 수소 제조공정의 대안 중 하나는 탄화수소연료의 수소와 탄소로의 직접분해에 의한 수소생산이다. 이 중 원하는 생성물인 수소 외에 부산물이 카본이 동시에 얻을 수 있는 메탄분해에 의한 수소생산방법은 생산된 수소의 약 15%만 연소시킴으로서 필요한 에너지를 공급할 수 있으며, 동시에 지구온난화의 주범인 CO 또는 $CO_2$가 생성되지 않는 장점이 있다. 하지만 메탄을 분해하기 위해서는 매우 높은 에너지가 필요로 하게 된다. 이에 반해 프로판은 메탄보다 낮은 열원에서 분해할 수 있는 장점을 지니고 있다. 본 연구에서는 메탄보다 분해하기 쉬운 프로판을 직접 분해하여 수소를 생산하고자 하였다. 프로판 직접분해반응는 $500\sim750^{\circ}C$의 온도 범위에서 이루어 졌으며, 촉매로서는 국내에서 생산되는 상용촉매인 카본블랙을 이용하였다.

• Journal of Korea Soil Environment Society
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• v.5 no.1
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• pp.97-108
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• 2000

A Gram-type negative bacteria that can utilize crude oil as the sole source of carbon and energy was isolated from an activated sludge of a local sewage treatment plant and identified tentatively as belonging to the genus Acinetobacter. The isolate could degrade n-alkanes and unidentified hydrocarbons in crude oil and utilize n-alkanes, hydrophobic substrates, as sole carbon and energy sources. n-Alkanes from tridecane (Cl3) to triacontane (C30) in crude oil were degraded simultaneously with no difference in degradation characteristics between the two close odd and even numbered alkanes in carbon numbers. The linear growth of the isolate and the degradation characteristics of Pr-alkanes suggested that the transport of substrates from the oil phase to the site where the substrates undergo the initial oxidation in microorganism might be the rate limiting in the biodegradation process of crude oil constituents. The remainder fraction of substrates after cultivation was considered to reflect the hydrocarbon inclusions in the cell mass, characteristics in Acinetobacter species, and to control the transport of substrates from crude oil phase. On the basis of the results, the isolate was considered to play an important role in the degradation study of hydrophobic environmental pollutants.