• 제목/요약/키워드: Oxidative reaction

검색결과 462건 처리시간 0.033초

망간산화물을 이용한 수용액내 Bisphenol-A의 산화 반응성 평가 (Application of Manganese Oxide for the Oxidative Degradation of Bisphenol-A in Aqueous Phase)

  • 지상현;고석오
    • 한국물환경학회지
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    • 제23권5호
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    • pp.659-664
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    • 2007
  • The objective of this study is to evaluate the detoxification method for the endocrine disrupting chemicals by manganese oxide. Manganese coated sand and bisphenol-A (BPA) was used as the reactive medium and the contaminant. Results showed that manganese oxide effectively degrades BPA by oxidative coupling reaction. The nonlinear oxidative coupling reaction orders were obtained for BPA and oxide, respectively. The reaction rate of BPA decreased as initial BPA concentration increased, as oxide loading decreased and as pH increased. The higher ionic strength, the higher reaction rate was observed. Divalent cations were adsorbed on the oxide surfaces, resulting in the decreased degradation rate of BPA.

Collagen 분자 중의 lysine 산화반응에 미치는 비타민 C의 영향 (The effect of L-Ascorbic Acid on the Oxidative Reaction of Lysine in Collagen.)

  • 김미향
    • 생명과학회지
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    • 제14권3호
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    • pp.478-483
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    • 2004
  • AsA 및 그 관련화합물, 각종 환원제 등을 첨가하여 lysine의 산화반응에 미치는 영향에 대하여 검토하였다. AsA의 첨가에 의해 lysyl oxidase활성의 지표인 과산화수소의 생성량은 대조군에 비하여 감소하였다. 2 $\mu$M의 AsA의 첨가에 의해 효소활성은 완전히 억제되었고, 0.2 $\mu$M 농도에서 억제효과가 나타났으나 40분 경과 후 다시 활성이 상승하는 경향이 나타났다. 또한 0.02$\mu$M 에서는 효소활성 의 변화는 대조군과 비슷한 경향을 나타내었다. 효소활성은 환원형 AsA에서 저해 효과가 높았으나 산화형 비타민 C (dehydroascorbic acid: DHA)와 환원제인 glutathione (GSH)에서는 억제효과가 크게 나타나지 않았다. AsA의 입체이성체인 ErA는 AsA와 같이 lysine 산화반응에서 억제적으로 작용하고 환원제인 GSH 보다도 lysyl oxidase에 미치는 영향은 큰 것으로 나타났다. 즉, lysine산화반응에 미치는 억제 효과는 환원제로서는 AsA와 ErA에서만 나타났으므로, 그 구조가 lysyl oxidase에 관여 할 가능성이 보여졌으므로, AsA의 analogue인 3,4-dihydro-xybenzoate를 이용하여 lysyl oxidase의 효소활성에 미치는 영향을 검토하였다. AsA의 analogue인 3,4-dihydroxyben-zoate를 첨가하였을 때에도 lysyl oxidase 활성은 억제되어, AsA의 analogue가 AsA와 같은 효과를 나타내었으므로 AsA의 endiol기의 작용 가능성을 추측할 수 있다. 이러한 결과로부터 lysine의 산화반응은 AsA에 의해 억제되고, 그 억제 효과는 AsA의 endiol기가 효소-구리이온 복합체를 환원할 때 효소의 활성부위에 접근하여 나타나는 것으로 사료된다.

Thermal Oxidative Purification of Detonation Nanodiamond in a Gas-Solid Fluidized Bed Reactor

  • Lee, Jae Hoon;Youn, Yong Suk;Lee, Dong Hyun
    • Korean Chemical Engineering Research
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    • 제56권5호
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    • pp.738-751
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    • 2018
  • The effect of the reaction temperature and reaction time on the thermal oxidative purification quality of detonation nanodiamond (NDsoot) was investigated in a gas-solid fluidized bed reactor of a $0.10m-ID{\times}1.0m$-high stainless steel column with zirconia beads ($d_{SV}=99.2{\mu}m$). The carbon conversion increased with increasing the reaction temperature; however, when the reaction temperature was greater than 773 K, the carbon conversion did not increase. The content of $sp^3$-hybridized carbon at the reaction temperature of 703 K barely changed when the reaction time was more than 30 minutes, but at 773 K, the content decreased as preferred. At 703 K, the purification quality increased with the increasing reaction time; however, at 773 K, the purification quality increased up to 30 minutes and then decreased rapidly.

Spectral and Mechanistic Investigation of Oxidative Decarboxylation of Phenylsulfinylacetic Acid by Cr(VI)

  • Subramaniam, Perumal;Selvi, Natesan Thamil;Devi, Soundarapandian Sugirtha
    • 대한화학회지
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    • 제58권1호
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    • pp.17-24
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    • 2014
  • The oxidative decarboxylation of phenylsulfinylacetic acid (PSAA) by Cr(VI) in 20% acetonitrile -80% water (v/v) medium follows overall second order kinetics, first order each with respect to [PSAA] and [Cr(VI)] at constant [$H^+$] and ionic strength. The reaction is acid catalysed, the order with respect to [$H^+$] is unity and the active oxidizing species is found to be $HCrO_3^+$. The reaction mechanism involves the rate determining nucleophilic attack of sulfur atom of PSAA on chromium of $HCrO_3^+$ forming a sulfonium ion intermediate. The intermediate then undergoes ${\alpha}$,${\beta}$-cleavage leading to the liberation of $CO_2$. The product of the reaction is found to be methyl phenyl sulfone. The operation of substituent effect shows that PSAA containing electron-releasing groups in the meta- and para-positions accelerate the reaction rate while electron withdrawing groups retard the rate. An excellent correlation is found to exist between log $k_2$ and Hammett ${\sigma}$ constants with a negative value of reaction constant. The ${\rho}$ value decreases with increase in temperature evidencing the high reactivity and low selectivity in the case of substituted PSAAs.

TiO2에 담지된 금속 산화물 촉매상에서 TCE 산화분해반응 (Oxidative Decomposition of TCE over TiO2-Supported Metal Oxide Catalysts)

  • 양원호;김문현
    • 한국환경과학회지
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    • 제15권3호
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    • pp.221-227
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    • 2006
  • Oxidative TCE decomposition over $TiO_2$-supported single and complex metal oxide catalysts has been conducted using a continuous flow type fixed-bed reactor system. Different types of commercial $TiO_2$ were used for obtaining the supported catalysts via an incipient wetness technique. Among a variety of titanias and metal oxides used, a DT51D $TiO_2\;and\;CrO_x$ would be the respective promising support and active ingredient for the oxidative TCE decomposition. The $TiO_2-based\;CrO_x$ catalyst gave a significant dependence of the catalytic activity in TCE oxidation reaction on the metal loadings. The use of high $CrO_x$ contents for preparing $CrO_x/TiO_2$ catalysts might produce $Cr_2O_3$ crystallites on the surface of $TiO_2$, thereby decreasing catalytic performance in the oxidative decomposition at low reaction temperatures. Supported $CrO_x$-based bimetallic oxide systems offered a very useful approach to lower the $CrO_x$ amounts without any loss in their catalytic activity for the catalytic TCE oxidation and to minimize the formation of Cl-containing organic products in the course of the catalytic reaction.

망간산화물을 이용한 1-Naphthol의 산화 제거 연구 (Oxidative Transformation of 1-Naphthol Using Manganese Oxide)

  • 임동민;강기훈;신현상
    • 대한환경공학회지
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    • 제28권5호
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    • pp.535-542
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    • 2006
  • 본 연구에서는 일반 토양 중에 존재하는 망간산화물의 하나인 버네사이트(birnessite)를 이용한 1-naphthol의 산화-공유결합 반응에 의한 제거 특성을 다양한 반응조건(반응시간, 버네사이트 주입량 및 pH 등)에서 회분식 실험을 통하여 조사하였다. 버네사이트에 의한 1-naphthol의 제거효율은 모든 반응조건에서 우수하였으며, 생성되는 반응산물은 1-naphthol의 산화-공유결합 반응에 의한 중합체임을 반응 후 상등액에 대한 UV-vis. 흡광 분석 및 질량분석기를 이용한 분자량 분석을 통해 확인하였다. 버네사이트 첨가량에 따른 1-naphthol의 산화 변환 실험 결과는 유사-일차 반응속도 식을 적용하여 반응 속도 상수, k를 구하였으며, 이 유사-일차 속도상수를 버네사이트의 비표면적으로 표준화하여 도출한 반응속도상수($k_{surf}$)는 $9.31{\times}10^{-4}(L/m^2{\cdot}min)$이었다. 또한, 버네사이트에 의한 1-naphthol의 산화 변환 효율은 수용액의 pH에 영향을 받았으며, pH가 10에서 4로 감소하면서 유사-일차 반응속도 상수는 $0.129min^{-1}$에서 $0.187min^{-1}$로 증가하였다.

망간산화물을 이용한 1-Naphthol의 산화-공유결합 반응 속도 연구

  • 임동민;신현상;전병우;강기훈
    • 한국지하수토양환경학회:학술대회논문집
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    • 한국지하수토양환경학회 2005년도 총회 및 춘계학술발표회
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    • pp.49-52
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    • 2005
  • In this study, abiotic transformation of 1-naphthol via oxidative-coupling reaction was evaluated using Mn oxide which is ubiquitous in natural soils. The transformation of 1-naphthol catalyzed by synthetic birnessite $({\delta}-MnO_2)$ followed pseudo-lst order reaction, and the rate constants was in the range of $0.053{\sim}0.13\;min^{-1}$ with birnessite loadings of $12.5{\sim}50\;mg/20\;mL$. Since the oxidation of 1-naphthol was occurred on the reactive surface of the oxide particles, the rate constants with various birnessite loadings were correlated with birnessite surface area concentration. The correlation showed a strong linearity, which confirms the supposition of the surface reaction. From the correlation, therefore, the surface area normalized rate constant, $k_{surf}$, was determined to be 0.032 $L/m^2\;min$.

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3-Methylthiophene이 함유된 폴리우레탄 필름의 전기적 특성 연구 (Electrical Properties and Characterization of 3-Methylthiophene Impregnated Polyurethane films)

  • 최세영;최교창;이은경
    • Elastomers and Composites
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    • 제39권3호
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    • pp.234-243
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    • 2004
  • 본 연구에서는 poly(propylene glycol) (PPG), toluene 2,4-diisocyanate, 3-methylthiophene (3-MT)으로부터 반응시간, $FeCl_3$의 농도, 3-MT와 PU의 무게비, 반응온도 등의 다양한 조건에 따라 전도성 폴리우레탄 필름을 제조하였다. $FeCl_3$와 ethyl acetate로 구성된 유기용매에 제조한 필름을 함침 시킨 결과 3-MT와 $FeCl_3$의 확산-산화 반응을 통해 급속한 전도성 PMT 층이 형성되었다. 전도성 복합체의 전기 전도도는 제조조건에 따라 많은 영향을 받고 SEM 분석과 접촉각 측정으로부터 반응시간과 반응온도가 모폴로지와 표면 자유에너지에 미치는 영향을 조사하였으며 제조된 복합체의 전도도는 최대 42 S/cm 인 것으로 확인되었다.

Role of Oxidative Stress in the Radiation-Induced Lung Pathogenesis in Mice

  • Park, Eun-Mi;Park, Ji-Sun;Kim, Yun-Jeong;Sung, Jae-Suk;Hwamg, Tea-Sook;Kim, Woo-Chul;Han, Mi-Young;Park, Young-Mee
    • BMB Reports
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    • 제34권6호
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    • pp.544-550
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    • 2001
  • In pre-transplant total-body irradiation (TBI), the lung is a critical dose-limiting organ. Also, the possible role of oxidative stress was suggested in the development of TBI-induced lung damage. This study explores the association between TBI-induced oxidative stress and the induction of lung pathogenesis by investigating TBI-induced oxidative stress in the lungs of male C57BL/6 mice after a single dose of 10 Gy TBI. We showed significant increases of reactive oxygen species (ROS) formation and lipid peroxidation, and also a depletion and oxidation of glutathione after TBI. There is evidence that pretreatment with 1,10-phenanthroline (o-phen) significantly reduces oxidative stress in the lung. This indicates that the TBI-induced ROS generation involves a metal-catalyzed Fenton-type reaction. A pretreatment of buthionine sulfoximine (BSO) augmented the glutathione depletion and oxidation, but had no effect on the ROS formation and lipid peroxidation up to 6 h after TBI. Histopathological features that are consistent with pneumonitis were observed in the BSO pretreated-mice 1 week after irradiation. The results suggest that TBI-induced oxidative stress in the lung involves a generation of ROS through a Fenton-type reaction. Also, glutathione plays an important inhibitory role in the radiation-induced lung pathogenesis by participating in the self-amplifying cascade subsequent to the ROS generation by irradiation.

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