• Title/Summary/Keyword: p-Xylene

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Measurement and Prediction of Autoignition Temperature (AIT) and Ignition Delay Time of n-Pentanol and p-Xylene Mixture (n-Pentanol p-Xylene 과 혼합물의 최소자연발화온도와 발화지연시간의 측정 및 예측)

  • Ha, Dong-Myeong
    • Fire Science and Engineering
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    • v.31 no.5
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    • pp.1-6
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    • 2017
  • The fire and explosion properties of combustible materials are necessary for the safe handling, storage, transportation and disposal. Typical combustion characteristics for process safety include auto ignition temperature(AIT). The AIT is an important index for the safe handling of combustible liquids. The AIT is the lowest temperature at which the material will spontaneously ignite. In this study, the AITs and ignition delay times of n-pentanol and p-xylene mixture were measured by using ASTM E659 apparatus. The AITs of n-pentanol and p-xylene which constituted binary system were $285^{\circ}C$ and $557^{\circ}C$, respectively. The experimental AITs and ignition delay times of n-pentanol and p-xylene mixture were a good agreement with the calculated AITs and ignition delay times by the proposed equations with a few A.A.D. (average absolute deviation). Therefore, it is possible to estimate the AITs and ignition delay times in other compositions of n-pentanol and p-xylene mixture by using the predictive equations which presented in this study.

Substrate Utilization Patterns During BTEX Biodegradation by an o-Xylene-Degrading Bacterium Ralstonia sp. PHS1

  • Lee, Sung-Kuk;Lee, Sun-Bok
    • Journal of Microbiology and Biotechnology
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    • v.12 no.6
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    • pp.909-915
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    • 2002
  • The biodegradation of BTEX components (benzene, toluene, ethylbenzene, o-xylene, m-xylene, and p-xylene) individually and in mixtures was investigated using the o-xylene-degrading thermo-tolerant bacterium Ralsronia sp. strain PHS1 , which utilizes benzene, toluene, ethylbenzene, or o-xylene as its sole carbon source. The results showed that as a single substrate for growth, benzene was superior to both toluene and ethylbenzene. While growth inhibition was severe at higher o-xylene concentrations, no inhibition was observed (up to 100 mg $l^-1$) with ethylbenzene. In mixtures of BTEX compounds, the PHS1 culture was shown to degrade all six BTEX components and the degradation rates were in the order of benzene, toluene, o-xylene, ethylbenzene, and m- and p-xylene. m-Xylene and p-xylene were found to be co-metabolized by this microorganism in the presence of the growth-supporting BTEX compounds. In binary mixtures containing the growth substrates (benzene, toluene, ethylbenzene. and o-xylene), PHS1 degraded each BTEX compound faster when it was alone than when it was a component of a BTEX mixture, although the degree of inhibition varied according to the substrates in the mixtures. p-Xylene was shown to be the most potent inhibitor of BTEX biodegradation in binary mixtures. On the other hand, the degradation rates of the non-growth substrates (m-xylene and p-xylene) were significantly enhanced by the addition of growth substrates. The substrate utilization patterns between PHS1 and other microorganisms were also examined.

A Study on the metabolism mechanism of Benzene, Toluene and Xylene by Cytochrome P-450 dependent radical-mediated (Cytochrome P-450 의존성 radical 전달에 의한 Benzene, Toluene, Xylene의 대사기전 연구)

  • 김기웅;장성근;김양호;문영한
    • Toxicological Research
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    • v.11 no.2
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    • pp.205-213
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    • 1995
  • This study was undertaken to investigate the effects of organic solvents on xenobiotic metabollzing enzyme system in vivo by meaas of experimental conditions i.e. (1) single group which was treated by benzene (B), toluene (T) and xylene (X), respectively, (2) combination group which was treated by mixture of benzene+toluene (BT), benzene+xylene (BX), and toluene+xylene (TX), respectively, (3) mixture group which was treated by benzene+ toluene+xylene mixture (M), and to interpreat the interaction between the organic solvents metabolizing enzymes. 1. The contents of cytochrome P-450 in liver microsomes were increased (p < 0.01) in organic solvents treated groups, and the contents of cytochrome P-450 were increased by following order of B < T < M < BT=BX < X < TX. 2. The activity of cytochrome P-450 dependent AHHase was significantly higher in organic solvents treated groups than in control group (p < 0.01), and the activity of AHHase was increased by following order of B < T < BT=BX=TX=xylene < M. 3. The activity of NADPH P-450 reductase was significantly higher in organic solvents treated groups than in control group (p < 0.01), and the order of M < combinated group < X < T

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Measurement and Prediction of Autoignition Temperature of n-Hexanol+p-Xylene Mixture (노말헥산올과 파라자일렌 혼합물의 최소자연발화온도 측정 및 예측)

  • Ha, Dong-Myeong
    • Journal of Energy Engineering
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    • v.25 no.1
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    • pp.48-55
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    • 2016
  • The autoignition temperature (AIT) of a material is the lowest temperature at which the material will spontaneously ignite. The AIT is important index for the safe handling of flammable liquids which constitute the solvent mixtures. This study measured the AITs of n-hexanol+p-xylene system by using ASTM E659 apparatus. The AITs of n-hexanol and p-xylene system which constituted binary system were $275^{\circ}C$ and $557^{\circ}C$, respectively. The experimental AITs of n-hexanol+p-xylene system system were a good agreement with the calculated AITs by the proposed equations with a few A.A.D.(average absolute deviation).

Measurement and Prediction of Autoignition Temperature of n-Butanol+p-Xylene Mixture (노말부탄올과 파라자일렌 혼합물의 최소자연발화온도 측정 및 예측)

  • Ha, Dong-Myeong
    • Journal of the Korean Institute of Gas
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    • v.20 no.5
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    • pp.1-8
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    • 2016
  • The autoignition temperature (AIT) of a substance is the lowest temperature at which the vapor ignites spontaneously from the heat of the environment. The AIT is important index for the safe handling of flammable liquids which constitute the solvent mixtures in the process. This study measured the AITs of n-butanol+p-xylene mixture by using ASTM E659 apparatus. The AITs of n-butanol and p-xylene which constituted binary system were $340^{\circ}C$ and $557^{\circ}C$, respectively. The experimental AITs of n-butanol+p-xylene mixture were a good agreement with the calculated AITs by the proposed equations with a few A.A.D.(average absolute deviation).

The Investigation of Biodegradation Characteristics of Xylene by Soil Inhabited Microorganisms (토양 서식 미생물을 이용한 자일렌(xylene) 분해특성 조사)

  • Choi, Phil-Kweon;Heo, Pyeung;Lee, Sang-Seob
    • Journal of Korean Society of Environmental Engineers
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    • v.35 no.6
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    • pp.389-393
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    • 2013
  • The purpose of this study is to investigate the biodegradation characteristics of the xylene by BTEX-degrading bacteria, Pseudomonas putida BJ10, isolated from oil-contaminated soil and bio-degradation pathway of the xylene. The removal efficiencies of o, m, p-xylene in mineral salts medium (MSM) by P. putida BJ10 were 94, 90 and 98%, respectively for 24 hours. It shows clear difference compared with the control groups which were below 3%. The removal efficiencies of BTEX by P. putida BJ10 in gasoline-contaminated soil were 66% for 9 days. They were clearly distinguished from the control groups (control and sterilized soil) which were 32 and 8%. 3-methylcatechol and o-toluic acid were detected after 6 and 24 hours during the o-xylene biodegradation pathway. Therefore, we confirmed o-toluic acid as the final metabolite. And intermediate-products were somewhat different with previously published studies of the transformation pathway from o-xylene to 3-methylcatechol.

Substrate Interactions on Biodegradation of Benzene, Toluene, Ethylbenzene and Xylene Isomers(BTEX) by Indigenous Soil Microorganisms (토양미생물을 이용한 Benzene, Toluene, Ethylbenzene 그리고 Xylene isomers(BTEX)의 분해시 기질반응)

  • La, Hyun-Joo;Chang, Soon-Woong;Lee, Si-Jin
    • Journal of Korean Society of Environmental Engineers
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    • v.22 no.2
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    • pp.375-383
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    • 2000
  • A mixed culture isolated from petroleum-contaminated soil was enriched on toluene as a sole carbon and energy source, and degradation characteristics of BTEX(Benzene, Toluene, Ethylbenzene, Xylenes) was observed. In the single-substrate experiments, all the BTEX compounds were degraded, and it was degraded as following orders; toluene, benzene, ethylbenzene, and p-xylene. In the degradation experiments of BTEX mixtures, the degradation rate was decreased compared to that in the single substrate experiment and ethylbenzene was degraded faster than benzene. In the experiments of binary-mixtures, various substrate interactions such as inhibition, stimulation, and non-interaction were observed, and ethylbenzene was shown to be most potent inhibitor of BTEX degradation. In the degradation characteristic studies of xylene isomers, m-xylene and p-xylene were degraded as carbon sources, and it was stimulated in the presence of either benzene or toluene. However, degradation of o-xylene was enhanced only in the presence of benzene.

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Liquid Phase Oxidation of Xylenes: Effects of Water Concentration and Alkali Metals

  • Jhung, Sung-Hwa;Lee, Ki-Hwa;Park, Youn-Seok
    • Bulletin of the Korean Chemical Society
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    • v.23 no.1
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    • pp.59-64
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    • 2002
  • A facile and precise batch oxidation reaction system allows continuous monitoring of the oxidation rate and cumulated oxygen conversion of xylenes, and the side reactions to carbon monoxide and carbon dioxide may also be studied. The oxidation reaction can be analyzed precisely with the rate and amount of oxygen consumed. The reaction reveals that 4-carboxybenzaldehyde is an unstable intermediate of p-xylene oxidation as the reaction proceeds instantaneously from p-toluic acid to TPA (terephthalic acid). The alkali metals accelerate oxidation, even though they retard the reaction initially. The oxidation rate increases with decreasing water concentration. However, in the later part of reaction, the reactivity decreases a bit if the water concentration is very low. This retarding effect of water can be overcome partly by the addition of potassium. The oxidation of o-xylene, compared with the oxidation of p-xylene and m-xylene, proceeds quite fast initially, however, the oxidation rate of xylene isomers in the later stage of reaction is in the order of p-xylene > mxylene > o-xylene.

Cometabolic Removal of Xylene Isomers by Alcaligenes xylosoxidans Y234

  • Yeom, Sung-Ho;Lee, Jung-Heon;Yoo, Young Je
    • Journal of Microbiology and Biotechnology
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    • v.8 no.3
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    • pp.222-228
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    • 1998
  • The characteristics of cometabolic removal of xylenes by Alcaligenes xylosoxidans Y234 were investigated. m-Xylene was found to be degraded while ο- and p-xylene were biotransformed into cresols in the presence of benzene or toluene. A lower level of benzene was required than that of toluene to remove the same amount of xylenes, which suggested benzene was a more effective primary substrate than toluene. ο-Xylene was found to be the most toxic to Alcaligenes xylosoxidans Y234 followed by p-xylene and m-xylene. Rates of cell decay during cometabolic removal of ο-, m-, or p-xylene were decreased by up to $76\%$ when benzene-adapted cells were inoculated. Xylenes were removed efficiently using benzene-adapted cells.

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Biodegradation of BTEX (benzene, toluene, ethylbenzene, xylene isomers) from organic solvent tolerant bacterium, Pseudomonas savastanoi BCNU 106

  • Kim, Jong-Su;Park, Hyeong-Cheol;Jo, Su-Dong;Kim, Gi-Uk;Bae, Yun-Wi;Mun, Ja-Yeong;Jeong, Yeong-Gi;Ju, U-Hong
    • 한국생물공학회:학술대회논문집
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    • 2003.04a
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    • pp.386-389
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    • 2003
  • Organic solvent tolerance bacteria, Pseudomonas savastanoi BCNU 106 could utilize a high contentration of benzene, toluene, ethylbenzene, xylene isomers (BTEX) as a sole carbon source. It was founded that strain BCNU 106 transformed o-xylene to 2-methylbenzyl alcohol, 2-methylbenzoic acid through direct oxygenation of methyl residue on GC-MS analysis.

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