• 제목/요약/키워드: photoreduction

검색결과 50건 처리시간 0.029초

Sulfite가 보리(Hordeum vulgare L.) 유식물의 녹화에 미치는 영향 (The Effects of Sulfite on the Greening of Etiolated Barley (Mordeum vuigare L.) Seedling)

  • 박강은;정화숙
    • 한국환경과학회지
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    • 제7권2호
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    • pp.133-140
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    • 1998
  • To investigate the effects of sulfite on the chloroplast development, etiolated barley seedlings were treated with 100 mM sulfite solution every 3 hour by spraying during 96 hours greening Period. The effects were determined by chlorophyll a, b and carotenoids contents, photosynthetic electron transport activity, chlorophyll fluorescence yield and fluorescence quenching parameters. The contents of chlorophyll a and carotenoids were decreased than that of control by treatment of salfite over 48 hours greening. PS II Is more sensitive to sulfite than PS I Is. And by the addition of DPC to the chloroplasts of the barley seedling treated with sulfite, the photoreduction of DCPIP was not recovered. In greening with suite treated barley leaves, Fo, Fv and Nlh ratio were decreased with little difference from that of control. But qP, qNP and qR were lowed in comparison with those of controls whereas qE was markedly higher than that of control. Especially, It is Interesting that qR was decreased markedly compared to that of control. The results in the change of PS I activity, Nf and qP suggest that the strate of Inhibition by suite Is carbon dioxide reduction cycle.

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Screening of antioxidant and antimicrobial activities of Caesalpinia bonducella Flem., leaves (Caesalpiniaceae)

  • Gupta, Malaya;Mazumdar, UK;Kumar, Ramanathan Sambath;Gomathi, Periyasamy;Rajeshwar, Y.;Kumar, T. Siva
    • Advances in Traditional Medicine
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    • 제4권3호
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    • pp.197-209
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    • 2004
  • The study was aimed at evaluating the antioxidant and antimicrobial activities of methanol extract of Caesalpinia bonducella leaves (MECB) (Family: Caesalpiniaceae). The effect of MECB on antioxidant activity, reducing power, free radical scavenging (DPPH radical, nitric oxide radical, superoxide anion radical, hydroxyl radical and hydrogen peroxide radical scavenging), total phenolic content and antimicrobial activities were studied. The antioxidant activity of MECB increased in a dose dependent manner. About 50, 100, 250 and 500 g of MECB showed 53.4, 61.2, 69.1 and 76.2 % inhibition respectively on peroxidation of linoleic acid emulsion. Like antioxidant activity, the effect of MECB on reducing power increased in a dose dependent manner. The free radical scavenging activity of MECB was determined by DPPH radical scavenging method. The potency of this activity was increased with increased amount of extract. MECB was found to inhibit the nitric oxide radicals generated from sodium nitroprusside $(IC_{50}\;=\;102.8\;g/ml)$ whereas the $IC_{50}$ value of curcumin was 20.4 g/ml. Moreover, the MECB was found to scavenge the superoxide generated by photoreduction of Riboflavin. MECB was also found to inhibit the hydroxyl radical generated by Fenton reaction, where the $IC_{50}$ value is 104.17 g/ml compared with catechin 5 g/ml, which indicates the antioxidant activity of MECB. The MECB capable of scavenging hydrogen peroxide in a concentration-dependent manner. The amounts of total phenolic compounds were also determined. Antimicrobial activities of MECB were carried out using disc diffusion methods with five Gram positive, four Gram negative and four fungal species. The results obtained in the present study indicate that MECB leaves are potential source of natural antioxidant and antimicrobial agents.

Development of Photo-Fenton Method for Gaseous Peroxides Determination and Field Observations in Gwangju, South Korea

  • Chang, Won-Il;Shim, Jae-Bum;Hong, Sang-Bum;Lee, Jai H.
    • Journal of Korean Society for Atmospheric Environment
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    • 제23권E1호
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    • pp.16-28
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    • 2007
  • An improved method was developed to determine gas-phase hydrogen peroxide($H_2O_2$) and organic hydro-peroxides (ROOH) in real-time, The analytical system for $H_2O_2$ is based on formation of hydroxybenzoic acid (OHBA), a strong fluorescent compound. OHBA is formed by a sequence of reactions, photoreduction of Fe(III)-EDTA to Fe(II)-EDTA, the Fenton reaction of Fe(II)-EDTA with $H_2O_2$, and hydroxylation of benzoic acid. By use of this analytical method rather than a previous similar method, Fenton reaction time was reduced from 2 min. to 30s. Air samples were collected by a surfaceless inlet to prevent inlet line losses. With a special arrangement of the sampling apparatus, sample delivery time was drastically reduced from ${\sim}5\;min\;to\;{\sim}20\;s$. The automated system was found to be sensitive, capable of continuous monitoring, and affordable to operate. A comparison of this method with a well-established one showed an excellent linear correlation, validating applicability of this technique to $H_2O_2$ determination. The system was applied to field measurements conducted during summertime of 2004 in Gwangju, South Korea. $H_2O_2$ was found to be a predominant species of peroxides. The diurnal variation of $H_2O_2$ displayed the maximum in early afternoon and the broad minimum throughout night. $H_2O_2$ was correlated positively with ozone, photochemical age, and temperature, however, negatively with $NO_x$ and relative humidity.

Metalloporphyrins 와 Polymer-bonded Metalloporphyrin 의 합성 및 Benzoquinone 광환원반응의 촉매효과 (Syntheses of Metalloporphyrins and Polymer-bonded Metalloporphyrin and Their Catalytic Effects on Benzoquinone Photoreduction)

  • 황규자;이희경;이용근
    • 대한화학회지
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    • 제35권5호
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    • pp.569-574
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    • 1991
  • pyrrole과 benzaldehyde 및 그 유도체로부터 meso-tetraphenylporphyrin(TPP)과 그 유도체 다섯가지를 합성한 후 이를 Co(II), Cu(II), Zn(II)의 염화물과 반응시켜 각각의 metalloporphyrin 착화합물을 만들고, 이 중 meso-tetra(p-aminophenyl)porphyrin(TNPP)을 다공성 polystyrene 수지와 반응시킨 후 여기에 Cu(II)의 염화물을 작용시켜 고분자결합 metalloporphyrin 착화합물 : Cu(Res-NH-TPP-$NH_2$)을 만들었다. 합성한 porthyrin 화합물들은 가시광선, 적외선 및 전자스핀공명 스펙트럼으로 확인하였고, 금속함량은 원자흡광 분광광도법으로 측정하였다. 합성한 porphyrin 화합물을 benzoquinone 광환원반응에 촉매로 이용한 결과, 일반적으로 유리 porphyrin보다 metalloporphyrin이, metalloporphyrin 중에는 Cu-TNPP의 촉매효과가 높았으며, 이에 고분자를 결합시키는 경우 효과가 더욱 향상됨을 알 수 있었다.

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졸-겔공정/광증착법을 이용한 Ag-Doped TiO2 합성 및 광촉매 특성 (Photocatalytic Properties of the Ag-Doped TiO2 Prepared by Sol-Gel Process/Photodeposition)

  • 김병민;김정식
    • 한국재료학회지
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    • 제26권2호
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    • pp.73-78
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    • 2016
  • $TiO_2$ nanoparticles were synthesized by a sol-gel process using titanium tetra isopropoxide as a precursor at room temperature. Ag-doped $TiO_2$ nanoparticles were prepared by photoreduction of $AgNO_3$ on $TiO_2$ under UV light irradiation and calcinated at $400^{\circ}C$. Ag-doped $TiO_2$ nanoparticles were characterized for their structural and morphological properties by X-ray diffractometry (XRD), scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), and transmission electron microscopy (TEM). The photocatalytic properties of the $TiO_2$ and Ag-doped $TiO_2$ nanoparticles were evaluated according to the degree of photocatalytic degradation of gaseous benzene under UV and visible light irradiation. To estimate the rate of photolysis under UV (${\lambda}=365nm$) and visible (${\lambda}{\geq}410nm$) light, the residual concentration of benzene was monitored by gas chromatography (GC). Both undoped/doped nanoparticles showed about 80 % of photolysis of benzene under UV light. However, under visible light irradiation Ag-doped $TiO_2$ nanoparticles exhibited a photocatalytic reaction toward the photodegradation of benzene more efficient than that of bare $TiO_2$. The enhanced photocatalytic reaction of Ag-doped $TiO_2$ nanoparticles is attributed to the decrease in the activation energy and to the existence of Ag in the $TiO_2$ host lattice, which increases the absorption capacity in the visible region by acting as an electron trapper and promotes charge separation of the photoinduced electrons ($e^-$) and holes ($h^+$). The use of Ag-doped $TiO_2$ nanoparticles preserved the option of an environmentally benign photocatalytic reaction using visible light; These particles can be applicable to environmental cleaning applications.

Pd/r-TiO2 나노튜브 이종결합 광촉매의 합성과 특성 (Synthesis and Characteristics of Pd/r-TiO2 Nanotube Arrays Hetrojunction Photocatalyst)

  • 이종호;이영기;김영직;장경욱;오한준
    • 한국재료학회지
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    • 제32권1호
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    • pp.14-22
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    • 2022
  • To improve light absorption ability in the visible light region and the efficiency of the charge transfer reaction, Pd nanoparticles decorated with reduced TiO2 nanotube photocatalyst were synthesized. The reduced TiO2 nanotube photocatalyst was fabricated by anodic oxidation of Ti plate, followed by an electrochemical reduction process using applied cathodic potential. For TiO2 photocatalyst electrochemically reduced using an applied voltage of -1.3 V for 10 min, 38% of Ti4+ ions on TiO2 surface were converted to Ti3+ ion. The formation of Ti3+ species leads to the decrease in the band gap energy, resulting in an increase in the light absorption ability in the visible range. To obtain better photocatalytic efficiency, Pd nanoparticles were decorated through photoreduction process on the surface of reduced TiO2 nanotube photocatalyst (r10-TNT). The Pd nanoparticles decorated with reduced TiO2 nanotube photocatalyst exhibited enhanced photocurrent response, and high efficiency and rate constant for aniline blue degradation; these were ascribed to the synergistic effect of the new electronic state of the TiO2 band gap energy induced by formation of Ti3+ species on TiO2, and by improvement of the charge transfer reaction.

2-할로벤질 페닐 에델의 광반응성 (The Photoreactivity of 2-Halobenzyl Phenyl Ether)

  • 박용태;김영희;신현일
    • 대한화학회지
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    • 제42권2호
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    • pp.203-208
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    • 1998
  • 할로겐화아렌이 다른 아렌에 etheral alkyl그룹에 의해 연결된 2-halobenzyl phenyl ether( 1과 2)를 합성하여 제조적인 광반응에서 생성물을 확인하고 또 속도론적 광반응에서 그 반응성을 시험하였다. 질소 기류 하에서 2-chlorobenzyl phenyl ether(1)은 페놀과 photo-Fries형 생성물이 나왔으며 Br치환 ether2는 페놀과 photo-Fries형 생성물 이외에 광고리화 및 광환원 생성물이 나왔다. 이것은 Cl이 benzyl고리에 강하게 붙어 있기 때문에 상대적으로 약한 $CH_{2}-O$결합의 파열이 생긴 결과이다. 또 Br유도체 2는 phenyl-bromine 사이의 결합이 phenyl-chlorine사이의 결합보다 약하니까 결국 그 결합의 광유발 파열이 $CH_{2}-O$결합 파열과 경쟁적으로 되었음이 분명하다. 산소 존재하에서 페놀의 생성은 큰 변화가 없고, photo-Fries형 생성물은 약간 감소하고 , 그리고 광고리화 생성물과 광환원 생성물은 큰 영향을 받는 것으로 보아 광고리화와 환원반응은 삼중상태가 상관하고 photo-fries형 반응은 단일상태와 삼중상태가 동시에 상관하는 것이다.

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은 이온과의 비교를 통한 나노 은 입자의 항균 특성 연구 (The Biocidal Activity of Nano-sized Silver Particles Comparing with Silver Ion)

  • 김지연;김성은;김재은;이종찬;윤제용
    • 대한환경공학회지
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    • 제27권7호
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    • pp.771-776
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    • 2005
  • 최근 항균 성능이 뛰어나면서도 인체에 유해하지 않은 나노 사이즈 은 입자를 이용한 항균 제품 개발 및 연구가 활발히 이루어지고 있음에 따라, 나노 사이즈의 은 입자를 보다 쉬운 방법으로 균일하게 제조하고, 그 특성을 평가하는데 많은 관심이 집중되고 있다. 본 연구에서는 은 이온의 광환원을 통해 나노 은 입자를 $15{\sim}20\;nm$ 크기로 균일하게 제조한 뒤, 나노 은 입자의 농도, pH, 온도가 변화함에 따른 항균 특성을 살펴보고 이를 정량적으로 평가, 은 이온의 항균 특성과 비교하였다. 또한 주사 전자 현미경과 투과 전자 현미경을 통하여 나노 은 입자의 미생물 불활성화 특성을 은 이온의 미생물 불활성화 특성과 비교하였다. 주요 결과로는 나노 은 입자의 항균 효과는 동일한 은 농도를 기준으로 하였을 때 은 이온의 항균 효과에 비하여 약 20배 정도 적은 것을 알 수 있었다. 또한 나노 은 입자의 농도, 온도가 높을수록 항균 성능은 향상됨을 알 수 있었으며 이는 은 이온의 실험 결과와 일치한다. 그러나 나노 은 입자의 항균 성능은 높은 pH에서 향상된 반면, 은 이온의 경우 pH 변화에 따른 항균 성능 변화가 관찰되지 않았다. 나노 은 입자와 은 이온에 의해 불활성화된 미생물을 주사 전자 현미경과 투과 전자 현미경으로 관찰한 결과, 나노 은 입자는 미생물 세포막을 크게 손상시키는 반면, 은 이온은 그렇지 않았다. 은 이온의 경우 은 이온이 미생물 안으로 흡수되어 세포질막을 손상시켜 미생물을 불활성화 시키는 것으로 알 수 있었다.

ESR 및 TRESR 分光法에 의한 Phenanthrenequinone의 光環元反應(I). Radical의 超微細分離常數에 미치는 溶媒效果 (A Photoreduction of Phenanthrenequinone by ESR and TRESR Spectroscopy(I)-Solvent Effect on Hyperfine-Splitting Constant of Radicals)

  • 홍대일;김창진
    • 대한화학회지
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    • 제37권3호
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    • pp.271-278
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    • 1993
  • 유기용매인 2-propanol, 2-pentanol 또는 benzene에 triethylamine을 혼합시켜 phenanthrenequinone을 포화시킨 용액에 Excimer laser(XeCl)를 쪼인 광환원반응에서 생성된 음이온 라디칼의 초미세 분리상수 전자스핀 공명분광법과 시간분애 전자스핀 공명분광법을 이용하여 얻었다. 그 결과 초미세분리상수 A$_{H1}$과 A$_{H2}$는 2-propanol에서 1.662, 0.378, 2-pentanol에서 1.602, 0.361 G이었고, benzene에서는 A$_{H1}$은 1.518이었다. 이와같이 혼합용매의 극성이 감소함에 따라 초미세 분리상수는 감소하였고, 비극성인 벤젠 혼합용매하에서는 자기적 등가양성자에 의한 작은 초미세분리(A$_{H2}$)는 측정할 수 없었다. 특히 2-pentanol과 triethylamine과의 3:1 혼합용매하에서 trietylamine radical(TEA${\cdot}$)이 0.15~0.30${\mu}s$ 시간범위의 시간분해 전자스핀공명 스펙트럼에서 phenanthrenequinone 음이온 라디칼과 함께 측정되었다. 이와같은 용매효과의 시간분해 전자스핀공명 스펙트럼의 측정 결과로부터 불안정한 짧은 수명의 반응중간체인 스핀편극된 phenanthrenequinone 음이온 라디칼(*PQ${\cdot}^-$)의 존재를 알 수 있었고, 각 혼합용매에서 초미세분리상수를 얻었다

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$TiO_2$-Encapsulated EFAL-Removed Zeolite Y as a New Photocatalyst for Photodegradation of Azo Dyes in Aqueous Solution

  • 조원재;윤숙자;윤민중
    • Journal of Photoscience
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    • 제12권1호
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    • pp.17-23
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    • 2005
  • Application of a new photocatalyst has been attempted to improve the efficiency and rates of photocatalytic degradation of azo dyes by using a model dye such as Methyl Orange. As a new photocatalyst, $TiO_2$ encapsulated EFAL-removed zeolite Y ($TiO_2$ /EFAL-removed zeolite Y) has been synthesized by ion-exchange in the mixture of EFAL-removed zeolite Y with 0.05 M aqueous [$(NH_4)_2 TiO(C_2O_4)_2.H_2O$] [$TiO(C_2O_4)_2.H_2O$]. This new photocatalyst has been characterized by measuring XRD, IR and reflectance absorption spectra as well as ICP analysis, and it was found that the framework structure of $TiO_2$ /EFAL-removed zeolite Y is not changed by removing the extra-framework aluminum (EFAL) from the normal zeolite Y and the $TiO_2$ inside the photocatalyst exists in the form of $(TiO^{2+})_n$ nanoclusters. Based on the ICP analysis, the Si/Al ratio of the $TiO_2$ /EFAL-removed zeolite Y and the weight of $TiO_2$ were determined to be 23 and 0.061g in 1.0g photocatalyst, respectively. It was also found that adsorption of the azo dye in the $TiO_2$ /EFAL-removed zeolite is very effective (about 80 % of the substrate used). This efficient adsorption contributes to the synergistic photocatalytic activities of the $TiO_2$ /EFAL-removed zeolite by minimizing the required flux diffusion of the substrate. Thus, the photocatalytic reduction of methyl orange (MO) was found to be 8 times more effective in the presence of $TiO_2$ /EFAL-removed zeolite Y than in the presence of $TiO_2$ /normal zeolite Y. Furthermore, the photocatalytic reduction of MO by using 1.0 g of the $TiO_2$ /EFAL-removed zeolite Y containing 0.061g of $TiO_2$ is much faster than that carried out by using 1.0 g of Degussa P-25.

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