• 제목/요약/키워드: Oxidation/Reduction Potential

검색결과 336건 처리시간 0.026초

${\kappa}-Carrageenan$ 필름을 사용하여 포장한 고등어육의 수분 손실 및 지방 산화 (Effects of ${\kappa}-Carrageenan$-Based Film Packaging on Moisture Loss and Lipid Oxidation of Mackerel Mince)

  • 황금택;임종환;박현진
    • 한국식품과학회지
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    • 제29권2호
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    • pp.390-393
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    • 1997
  • 2% ${\kappa}-carrageenan$, 0.1% KCl, 0.75%, PEG, 및 0.75% glycerol을 사용하여 제조한 필름을 고등어육의 포장재로 사용 가능성을 시험하기 위하여 포장 후 수분 손실 및 지방 산화의 정도를 측정하였다. 고등어육을 carrageenan 필름으로 포장하여 $20^{\circ}C,\;10^{\circ}C,\;0^{\circ}C$, 및 $-15^{\circ}C$에 저장하였으며, 포장하지 않은 시료도 $0^{\circ}C$에 저장하면서, 무게 감소, PV, TBA가 등을 측정하였다. $20^{\circ}C,\;10^{\circ}C$, 및 $0^{\circ}C$에 저장한 포장 또는 비포장 시료는 저장 후 15일 이내에 60%의 무게 감소 현상을 보였으나, $-15^{\circ}C$에 저장한 시료는 25일 후에도 약 3% 정도만의 무게 감소가 있었다. 포장하지 않은 채 $0^{\circ}C$에 저장한 시료는 지방 산화가 꾸준히 증가하는 현상을 보였는데, PV는 20일만에 23 mequivalent peroxide (PO)/㎏, TBA가는 5일만에 $0.4\;{\mu}mole$ malonaldehyde (MA)/g에 도달한 반면, carrageenan 필름으로 진공 포장한 어육은 28일간의 저장기간 동안 저장 온도에 관계없이 PV 및 TBA가가 각각 2 mequivalent PO/kg 및 $0.4\;{\mu}mole\;MA/g$ 이하를 나타냈다.

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가막만 표층퇴적물 중 알칼리 및 알칼리 토금속 원소의 생지화학적 특성 (Biogeochemistry of Alkaline and Alkaline Earth Elements in the Surface Sediment of the Gamak Bay)

  • 김평중;박승윤;김상수;장수정;전상백;주재식
    • 해양환경안전학회지
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    • 제18권1호
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    • pp.1-13
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    • 2012
  • 2010년 4월 가막만 전역의 19개 정점에서 표층퇴적물을 채취하여 퇴적물의 입도 분포, 유기물의 기원, 알칼리 원소(Li, Na, K, Rb) 및 알칼리 토금속(Be, Mg, Ca, Sr, Ba)원소의 분포특성을 파악하였다. 조사해역의 퇴적물 유형은 대부분 Mud로 나타났다. Chlorophyll $a$, TOC, TN, TS 및 LOI의 경우 만의 북부해역과 어류양식장이 산재되어 있는 남측해역에서 높은 농도분포를 보였으며, 만의 중앙부에서 낮은 농도를 보였다. 이들 성분과는 반대로 산화환원전위의 경우 만의 중앙부에서 대체로 (+)값으로 산화상태를 나타내었으며, 만의 북부해역과 남측해역에서 (-)상태로 환원환경 특성을 보였다. 유기물의 기원은 대부분 자생기원 유기물질 이였으나, 일부 정점에서 육상 및 박테리아성 유기물 기원 특성을 보였다. 알칼리 및 알카리 토금속 원소 중 Li, Na, K, Rb, Be, Mg, Ca 및 Sr의 경우 대부분의 정점에서 석영희석 효과에 의해 일차적으로 농도 분포가 결정된다. Ba의 경우 본 조사해역에서 중정석(Barite)가 존재하는 것으로 생각되며, Sr 및 Ba의 경우 이차적으로 탄산염 희석과 산화환원전위에 의한 생지화학적 영향을 직간접적으로 받는 것으로 보인다.

효모를 사용한 한지직물의 천연인디고 염색 : 효모농도와 반복염색 효과 (Natural Indigo Dyeing of Hanji Fabric using Baker's Yeast: Effect of Yeast Concentration and Repeat Dyeing)

  • 손경희;신윤숙;류동일
    • 한국염색가공학회지
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    • 제33권4호
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    • pp.191-201
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    • 2021
  • In this study, an eco-friendly indigo reduction system(scale up reduction, use of buffer solution, and pH control) using baker's yeast(Saccharomyces cerevisiae) was applied for natural indigo(Polygonum tinctorium) dyeing of Hanji fabric and Hanji-mixture fabric(Hanji/Cotton, Hanji/Silk). The effect of concentration of baker's yeast, repeat dyeing, and bath reuse was investigated in terms of dye uptake indicating reduction power. And the oxidation-reduction potential(ORP) was monitored. We also evaluated color properties and colorfastness according to the color strength. The yeast concentration did not significantly affect the maximum reduction power. However, the highest yeast concentration was effective in improving the initial dye uptake, and its the reduction retention power was the most excellent. Even on the last reduction day, the effect of increasing the dye uptake by repeat dyeing was observed. And it was confirmed that the reduction bath could be reused for up to 30 days by supplementing yeast at the end of reduction. For all the fabrics used, deeper and darker PB color were obtained by repeat dyeing. As dyeing was repeated, purplish tint got stronger on the Hanji/Silk fabric compared to other fabrics. Regardless of the composition of Hanji fabrics and color strength, washing and dry cleaning fastness were relatively good with above rating 4-5, and fastness to rubbing and light were acceptable with a rating 3-4 ~ 4-5. The eco-friendly natural indigo dyeing process using niram and baker's yeast would offer global marketability and diversity of Hanji product as a sustainable high value-added material.

Production of (R)-Ethyl-4-Chloro-3-Hydroxybutanoate Using Saccharomyces cerevisiae YOL151W Reductase Immobilized onto Magnetic Microparticles

  • Choo, Jin Woo;Kim, Hyung Kwoun
    • Journal of Microbiology and Biotechnology
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    • 제25권11호
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    • pp.1810-1818
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    • 2015
  • For the synthesis of various pharmaceuticals, chiral alcohols are useful intermediates. Among them, (R)-ethyl-4-chloro-3-hydroxybutanoate ((R)-ECHB) is an important building block for the synthesis of L-carnitine. (R)-ECHB is produced from ethyl-4-chloro-3-oxobutanoate (ECOB) by a reductase-mediated, enantioselective reduction reaction. The Saccharomyces cerevisiae YOL151W reductase that is expressed in Escherichia coli cells exhibited an enantioselective reduction reaction toward ECOB. By virtue of the C-terminal His-tag, the YOL151W reductase was purified from the cell-free extract using Ni2+-NTA column chromatography and immobilized onto Ni2+-magnetic microparticles. The physical properties of the immobilized reductase (Imm-Red) were measured using electron microscopy, a magnetic property measurement system, and a zeta potential system; the average size of the particles was approximately 1 μm and the saturated magnetic value was 31.76 emu/g. A neodymium magnet was used to recover the immobilized enzyme within 2 min. The Imm-Red showed an optimum temperature at 45℃ and an optimum pH at 6.0. In addition, Bacillus megaterium glucose dehydrogenase (GDH) was produced in the E. coli cells and was used in the coupling reaction to regenerate the NADPH cofactor. The reduction/oxidation coupling reaction composed of the Imm-Red and GDH converted 20 mM ECOB exclusively into (R)-ECHB with an e.e.p value of 98%.

ELECTROCHROMIC BEHAVIOR OF AMORPHOUS NICKELPHTHALOCYANINE THIN FILMS

  • Masui, Masayoshi;Suzuki, Masato;Kaneko, Fujio;Takeuchi, Manabu
    • 한국표면공학회지
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    • 제29권6호
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    • pp.735-738
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    • 1996
  • Amorphous nickelphthalocyanine(NiPc) thin films were prepared by vacuum evaporation and their electrochromic behavior and voltammograms were examined in the five kinds of aqueous electrolytes. Amorphous NiPc films were prepared on indium-tin-oxide(ITO) glass substrates cooled to-$120^{\circ}C$ by using liquid nitrogen under a vacuum of $2.4 \times 10^{-4}$. The voltammetric and electrochromic measurements were made using a potential galvanostat. In order to confirm the color change, optical vis-transmission spectra of the NiPc films were measured by a spectrophotometer with various electrode potential applied. The NiPc amorphous thin films exhibited most clearly electrochromism in $KNO_3$ aqueous electrolyte. The specimen films underwent 3 color transitions (from blue to yellow-green, then to red violet, then to dark blue), corresponding to the three peaks on the voltammograms in $KNO_3$ aqueous electrolyte. Blue is color of the as-prepared film. When the potential was swept, charge compensation was attained upon oxidation by injection of anions from the electrolyte and upon reduction by expulsion of anions.

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Electrochemical oxidation-reduction and determination of urea at enzyme free PPY-GO electrode

  • Mudila, Harish;Prasher, Parteek;Rana, Sweta;Khati, Beena;Zaidi, M.G.H.
    • Carbon letters
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    • 제26권
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    • pp.88-94
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    • 2018
  • This manuscript explains the effective determination of urea by redox cyclic voltammetric analysis, for which a modified polypyrrole-graphene oxide (PPY-GO, GO 20% w/w of PPY) nanocomposite electrode was developed. Cyclic voltammetry measurements revealed an effective electron transfer in 0.1 M KOH electrolytic solution in the potential window range of 0 to 0.6 V. This PPY-GO modified electrode exhibited a moderate electrocatalytic effect towards urea oxidation, thereby allowing its determination in an electrolytic solution. The linear dependence of the current vs. urea concentration was reached using square-wave voltammetry in the concentration range of urea between 0.5 to $3.0{\mu}M$ with a relatively low limit of detection of $0.27{\mu}M$. The scanning electron microscopy was used to characterize the morphologies and properties of the nanocomposite layer, along with Fourier transform infrared spectroscopy. The results indicated that the nanocomposite film modified electrode exhibited a synergistic effect, including high conductivity, a fast electron-transfer rate, and an inherent catalytic ability.

Polyol Process를 통한 PEM Fuel Cell용 Pt/C촉매 제조 (Preparation of Pt/C catalyst for PEM fuel cells using polyol process)

  • 오형석;김한성
    • 한국신재생에너지학회:학술대회논문집
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    • 한국신재생에너지학회 2006년도 추계학술대회
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    • pp.443-446
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    • 2006
  • Carbon-supported Platinum (Pt) is the potential electro-catalyst material for anodic and cathodic reactions in fuel cell. Catalytic activity of the metal strongly depends on the particle shape, size and distribution of the metal in the porous supportive network. Conventional preparation techniques based on wet impregnation and chemical reduction of the metal precursors often do not provide adequate control of particle size and shape. We have proposed a novel route for preparing nano sized Pt colloidal particles in solution by oxidation of ethylene glycol. These Pt nano particles were deposited on large surface area carbon support. The process of nano Pt colloid formation involves the oxidation of solvent ethylene glycol to mainly glycolic acid and the presence of its anion glycolate depends on the solution pH. In the process of colloidal Pt formation glycolate actsas stabilizer for the Pt colloidal particle and prevents the agglomeration of colloidal Pt particles. These mono disperse Pt particles in carbon support are found uniformly distributed in nearly spherical shape and the size distribution was narrow for both supported and unsupported metals. The average diameter of the Pt nano particle was controlled in the range off to 3 nm by optimizing reaction parameters. Transmission electron microscopy, CV and RRDE experiments were used to compliment the results.

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인지질(DOPC)과 지방산(8A5H)의 혼합 LB막의 광이성질화 현상과 전기화학적 특성 (Electrochemical Properties and Photoisomerization of DOPC-8A5H Mixture Langmuir-Blogett Films)

  • 박근호;최성현;김남석;김덕술
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 2004년도 하계학술대회 논문집 Vol.5 No.2
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    • pp.874-877
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    • 2004
  • We carried out this subject to observe electrochemical properties of 1,2-dioleoyl-sn- glycero-3-phosphocholine(DOPC) mixed with fatty acid containing azobenzene group by using cyclic voltammetry with a three-electrode system, An Ag/AgCl reference electrode, a platinum wire counter electrode and LB film-coated ITO working electrode in $NaClO_4$ solution. We investigated the photoisomerization and electrochemical property of the organic ultra thin film of fatty acid containing azobenzene was prepared on the hydrophilic ITO(idium tin oxide) glass plate by LB method. As a result, the absorption spectra of BASH and DOPC of mixture LB films was induced to photoisomerization by alternating irradiation of ultraviolet and visible light. A measuring range was reduced from initial potential to -1350mV, continuously oxidized to 1650 mV and measured to the initial point. The scan rate were 50, 100, 150 and 200 mV/s. As a results, LB films of BASH-DMPC appeared reversible process caused by the reduction-oxidation current from the cyclic voltammogram.

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Enhanced Photocatalytic Activity of TiO2 Modified by e-Beam Irradiation

  • Kim, Moon Su;Jo, Won Jun;Lee, Dowon;Baeck, Sung-Hyeon;Shin, Joong Hyeock;Lee, Byung Cheol
    • Bulletin of the Korean Chemical Society
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    • 제34권5호
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    • pp.1397-1400
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    • 2013
  • The influence of electron beam irradiation on photocatalytic activity of $TiO_2$ thin films was investigated. $TiO_2$ thin films were prepared by anodization of Ti foil, and they were then subjected to an 1 MeV electron beam. Changes in physical properties and photocatalytic activity of $TiO_2$ before and after e-beam irradiation were investigated. The crystallinity of the synthesized materials was investigated by X-ray diffraction, and the oxidation states of both titanium and oxygen were determined by X-ray photoelectron spectroscopy (XPS). The density of donor ($N_d$) and flat band potential ($E_{fb}$) were investigated by Mott-Schottky analysis, and photocurrent was measured under a 1kW Xenon lamp illumination. After e-beam irradiation, significant change of Ti oxidation state was observed. $Ti^{3+}/Ti^{4+}$ ratio increased mainly due to the surface reduction by electron, and photocurrent was observed to increase with e-beam irradiation.

Electrochemical Investigation of Acetaminophen with a Carbon Nano-tube Composite Film Electrode

  • Li, Chunya;Zhan, Guoqing;Yang, Qingdan;Lu, Jianjie
    • Bulletin of the Korean Chemical Society
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    • 제27권11호
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    • pp.1854-1860
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    • 2006
  • Electrochemical behaviors of acetaminophen at a muti-wall carbon nano-tube composite film modified glassy carbon electrode were investigated by cyclic voltammetry, linear sweep voltammetry and chronocoulometry. Compared with that obtained at the unmodified electrode, the peak currents were enhanced significantly, and the oxidation peak shifted towards more negative potential with the reduction peak shifted positively. The peak-to-peak separation turned narrow, and suggested that the reversibility was improved greatly. Experimental parameters, such as scan rate, pH and accumulation conditions were optimized. It was found that a maximum current response can be obtained at pH = 5.0 after accumulation at -0.50 V for 80 s. The oxidation peak current was found to be linearly related to acetaminophen concentration over the range of $5.0{\times}10^{-7}\;\sim\;1.0{\times}10^{-4}$ mol $L^{-1}$ with a detection limit of $5.0{\times}10^{-8} $mol $L^{-1}$. A convenient and sensitive electrochemical method was developed for the determination of acetaminophen in a commercial paracetamol oral solution. Its practical application demonstrated that it has good selectivity and high sensitivity.