• 제목/요약/키워드: oxidation characterization

검색결과 404건 처리시간 0.032초

동·식물성 유지를 이용한 바이오디젤 생산에 관한 연구 (Yield and Characterization of Various Biodiesel from Vegetable Oils and Animal Fats)

  • 이태성;이영화;김광수;김욱;김관수;장영석;박광근
    • 신재생에너지
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    • 제8권4호
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    • pp.30-37
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    • 2012
  • Biodiesel was produced by "transesterification" of vegetable oils and animal fats as an alternative to petroleum diesel. The research analysed the fuel characteristics of biodiesel, the yield of by-products and biodiesel, using several vegetable oils - rapeseed oil, camellia oil, peanut oil, sesame oil, perilla oil, palm oil, olive oil, soybean oil, sunflower oil and animal fats such as lard, tallow, and chicken fat. The results showed the yields of biodiesel made from the vegetable oils and animal fats were $90.8{\pm}1.4{\sim}96.4{\pm}0.9%$ and $84.9{\pm}1.1{\sim}89.6{\pm}1.5%$ respectively. Production rates and oxidation characteristics were different depending on the fats applied.

구룡광산 광미층의 심도변화에 따른 물리.화학적 및 광물학적 특성 (Physio-chemical and Mineralogical Characterization of the Tailings in the Guryoung Mining Area)

  • 문용희;김정연;송윤구;문희수
    • 자원환경지질
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    • 제41권2호
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    • pp.183-199
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    • 2008
  • 본 연구에서는 구룡광산에 적치된 광미층으로 부터 채취된 대표 비교란 코어시료를 대상으로 체계적인 물리 화학적 및 광물학적 특성을 심도별로 정량적으로 파악, 중금속 거동 핵심 영향요소를 기준으로 광미층 수직분대를 시도하고, 이를 기초로 광미층 비포화대-포화대에 걸친 원소 거동과 지화학적 조건과의 상관모델을 제시하고자 한다. 구룡광산의 대상 광미층은 화학적으로 지하수면을 경계로 상부층 구간에서의 낮은 pH(4)와 20wt.% 이상의 높은 $Fe_2O_3$$SO_3$ 함량에 의해 특징지어진다. 물리 화학적 및 광물학적 분석 자료를 고려하여 구룡광산 광미층을 심도증가에 따라 복토층, jarosite zone, Fe-sulfate zone, Fe-oxyhydroxide zone, gypsum-bearing pyrite zone, calcite-bearing pyrite zone, soil zone(광미층 집적 이전 토양층), weathered zone 등 7개분대로 구분할 수 있으며, 새로 생성된 이차광물상의 특성을 고려할 때 지하수면을 기준으로 상부층을 산화대(oxidation zone)로, 하부층을 비산화대(unoxidation zone), 혹은 carbonate-rich primary zone으로 크게 대분할 수 있다. 본 연구결과를 기초로 구룡광산 광미층의 물리 화학적 및 광물학적 변화를 지하수면 상부층에서의 황화광물, 특히 황철석의 산화반응이 핵심요소가 되어, 이로 인한 pH 값의 감소, 일차광물의 용해반응 및 원소 용출, 이차광물상 생성, 그리고 생성된 산의 탄산염 및 규산염광물에 의한 산-중화반응 등 일련의 지화학적 반응으로 설명할 수 있다.

Biochemical Characterization of the Dual Positional Specific Maize Lipoxygenase and the Dependence of Lagging and Initial Burst Phenomenon on pH, Substrate, and Detergent during Pre-steady State Kinetics

  • Cho, Kyoung-Won;Jang, Sung-Kuk;Huon, Thavrak;Park, Sang-Wook;Han, Ok-Soo
    • BMB Reports
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    • 제40권1호
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    • pp.100-106
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    • 2007
  • The wound-inducible lipoxygenase obtained from maize is one of the nontraditional lipoxygenases that possess dual positional specificity. In this paper, we provide our results on the determination and comparison of the kinetic constants of the maize lipoxygenase, with or without detergents in the steady state, and characterization of the dependence of the kinetic lag phase or initial burst, on pH, substrate, and detergent in the pre-steady state of the lipoxygenase reaction. The oxidation of linoleic acid showed a typical lag phase in the pre-steady state of the lipoxygenase reaction at pH 7.5 in the presence of 0.25% Tween-20 detergent. The reciprocal correlation between the induction period and the enzyme level indicated that this lag phenomenon was attributable to the slow oxidative activation of Fe (II) to Fe (III) at the active site of the enzyme as observed in other lipoxygenase reactions. Contrary to the lagging phenomenon observed at pH 7.5 in the presence of Tween-20, a unique initial burst was observed at pH 6.2 in the absence of detergents. To our knowledge, the initial burst in the oxidation of linoleic acid at pH 6.2 is the first observation in the lipoxygenase reaction. Kinetic constants (Km and kcat values) were largely dependent on the presence of detergent. An inverse correlation of the initial burst period with enzyme levels and interpretations on kinetic constants suggested that the observed initial burst in the oxidation of linoleic acid could be due to the availability of free fatty acids as substrates for binding with the lipoxygenase enzyme.

Synthesis and Characterization of CNT / TiO2 Photoelectrocatalytic Electrodes for Methlene Blue Degradation

  • Zhang, Feng-Jun;Chen, Ming-Liang;Oh, Won-Chun
    • 한국재료학회지
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    • 제18권11호
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    • pp.583-591
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    • 2008
  • In this study, two series of CNT/$TiO_2$ electrodes were prepared. The decrease of surface area compared with that of the pristine carbon nanotubes (CNTs) indicated the blocking of micropores on the surface of the CNTs; was further supported by scanning electron microscopy (SEM) and field emission SEM (FE-SEM) observations. The X-ray diffraction (XRD) results showed that the CNT/$TiO_2$ composites contained a mix of anatase and rutile forms of $TiO_2$ particles when the precursor was $TiO_2$ powder, whereas when the precursor was Ti ($OC_4H_7$) (TNB), the composites contained only the typical single and clear anatase $TiO_2$ particles. The energy dispersive X-ray spectroscopy (EDX) spectra showed the presence of C, O and Ti peaks for all samples. It was found that catalytic decomposition of methylene blue (MB) solution could be attributed to synthetic effects between the $TiO_2$ photocatalysis and electro-assisted CNTs network, and that photoelectrocatalytic oxidation increased with an increase of CNT composition. It was also found that the photoelectrocatalytic oxidation efficiency for MB is higher than that of photocatalytic oxidation. Moreover, the CNT/$TiO_2$ composites catalyst prepared by the impregnation method demonstrates higher photoelectrocatalytic activity than the mechanical mixture with the same CNT content.

다양한 환경조건을 가진 토양의 메탄산화세균 군집 특성 (Characterization of Methanotrophic Communities in Soils from Regions with Different Environmental Settings)

  • 김태관;박현정;이상현;김평화;문경은;조경숙
    • 한국미생물·생명공학회지
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    • 제40권2호
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    • pp.152-156
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    • 2012
  • 서울 근교의 민물 습지(FW), 해수습지(SW), 산림 토양(FS) 그리고 매립지 복토(LS)의 메탄산화세균 군집을 clone library/sequencing 기법을 이용하여 분석하였다. 메탄산화세균인 Methylocaldum, Methlyococcus과 Methylosinus는 FS와 SW에서 풍부하였으며, Methylobacter와 Methylomonas는 FW에서 풍부하였고, Methylocystis와 Methylomicrobium은 LS에서 우점하였다. 메탄 산화가 관찰되기 전까지 필요한 lag phase는 각 토양별로 유의적으로 차이가 있었고, 메탄 산화속도는 $FW{\geq}LS{\geq}SW>FS$순이었다. 이러한 결과들은 토양의 환경조건은 메탄산화세균의 군집과 메탄산화능에 영향을 미치는 중요한 인자임을 시사한다.

철 및 망간 산화물로 코팅된 입자활성탄을 이용한 수용액 중 As(III) 및 As(V)의 제거 (Removal of As(III) and As(V) in Aqueous Phases by Fe and Mn Oxides Coated Granular Activated Carbon)

  • 이희용;양중석;최재영;이승목
    • 대한환경공학회지
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    • 제31권8호
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    • pp.619-626
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    • 2009
  • 본 연구에서는 수용액상의 비소를 산화 및 흡착기작을 이용하여 제거하기 위해서 철과 망간 산화물로 코팅된 입자 활성탄 (FMOCG)을 제조하고, 이의 표면특성 및 회분식 실험을 통하여 비소제거 특성을 규명하였다. 회분식 실험에서는 네 가지 코팅매질의 비소 산화 및 흡착 동역학, pH 영향, 등온흡착실험을 실시하였다. 코팅매질의 철과 망간 함량은 FMOCG-1(178.12 Fe mg/g, 11.25 Mn mg/g)가 비교적 많은 것으로 나타났다. 비소흡착 동역학을 통하여 As(III)의 경우 산화 및 흡착을 통하여 제거됨을 확인하였다. pH 영향실험 결과 pH가 낮을수록 비소의 제거율이 높아지는 것으로 나타났다. 등온흡착실험 결과는 Langmuir isotherm에 잘 적용되었으며 As(III)보다 As(V)의 흡착량이 약간 높았으며, 최대 흡착량은 1.38~8.44 mg As(III)/g과 2.91~9.63 mg As(V)/g이었다.

Purification and Characterization of a Cyclohexanol Dehydrogenase from Rhodococcus sp. TK6

  • Kim, Tae-Kang;Choi, Jun-Ho;Rhee, In-Koo
    • Journal of Microbiology and Biotechnology
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    • 제12권1호
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    • pp.39-45
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    • 2002
  • Activity staining on the native polyacrylamide gel electrophoresis (PAGE) of a cell-free extract of Rhodococcus sp. TK6, grown in media containing alcohols as the carbon source, revealed at least seven isozyme bands, which were identified as alcohol dehydrogenases that oxidize cyclohexanol to cyclohexanone. Among the alcohol dehydrogenases, cyclohexanol dehydrogenase II (CDH II), which is the major enzyme involved in the oxidation of cyclohexanol, was purified to homogeneity. The molecular mass of the CDH II was determined to be 60 kDa by gel filtration, while the molecular mass of each subunit was estimated to be 28 kDa by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). The CDH II was unstable in acidic and basic pHs, and rapidly inactivated at temperatures above $40^{\circ}C$ . The CDH II activity was enhanced by the addition of divalent metal ions, like $Ba^2+\;and\;Mg^{2+}$. The purified enzyme catalyzed the oxidation of a broad range of alcohols, including cyclohexanol, trans-cyclohexane-1,2-diol, trans-cyclopentane-l,2-diol, cyclopentanol, and hexane-1,2-diol. The $K_m$ values of the CDH II for cyclohexanol, trans-cyclohexane-l,2-diol, cyclopentanol, trans-cyclopentane-l,2-diol, and hexane-l,2-diol were 1.7, 2.8, 14.2, 13.7, and 13.5 mM, respectively. The CDH II would appear to be a major alcohol dehydrogenase for the oxidation of cyclohexanol. The N-terminal sequence of the CDH II was determined to be TVAHVTGAARGIGRA. Furthermore, based on a comparison of the determined sequence with other short chain alcohol dehydrogenases, the purified CDH II was suggested to be a new enzyme.

Carbamate-Based Surface Reactions for Release of Amine Molecules from Electroactive Self-Assembled Monolayers

  • Hong, Dae-Wha;Kang, Kyung-Tae;Hong, Seok-Pyo;Shon, Hyun-Kyong;Lee, Tae-Geol;Choi, In-Sung S.
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2011년도 제41회 하계 정기 학술대회 초록집
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    • pp.208-209
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    • 2011
  • In this work, we developed self-assembled monolayers (SAMs) of alkanethiols on gold that can release amine groups, when an electrical potential was applied to the gold. The strategy was based on the introduction of the electroactive carbamate group, which underwent the two-electron oxidation with simultaneous release of the amine molecules, to alkanethiols. The synthesis of the designed thiol compounds was achieved by coupling isocyanate-containing compound with hydroquinone. The electroactive thiols were mixed with hydroxyl-containing alkanethiol [$HS(CH_2)_{11}OH$] to form mixed monolayers, and cyclic votammetry was used for the characterization of the release. The mixed SAMs showed a first oxidation peak at +540 mV (versus Ag/AgCl reference electrode), demonstrating irreversible conversion from carbamate to hydroqinone with simultaneous release of the amine groups. The second and third cycles showed typical reversible redox reaction of hydroquinone and quione: the oxidation and reduction occurred at +290 mV and -110 mV, respectively. The measurement of ToF-SIMS further indicates that electrochemical-assisted chemical reaction successfully released amine groups. This new SAM-based electrochemistry would be applicable for direct release of biologically active molecules that contain amine groups.

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습식분쇄공정에서 액상매체가 실리콘 분쇄 및 산화특성에 미치는 영향 (The Effect of Liquid Medium on Silicon Grinding and Oxidation during Wet Grinding Process)

  • 권우택;김수룡;김영희;이윤주;신동근;원지연;오세천
    • 한국세라믹학회지
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    • 제51권2호
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    • pp.121-126
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    • 2014
  • The influence of a liquid medium duringa wet-milling process in the grinding and oxidation of silicon powder was investigated. Distilled water, dehydrated ethanol and diethylene glycol were used as the liquid media. The applied grinding times were 0.5, 3, and 12 h. Ground silicon powder samples were characterized by means of aparticle size analysis, scanning electron microscopy(SEM), x-ray powder diffraction (XRD), FT-IR spectroscopy and by a chemical composition analysis. From the results of the characterization process, we found that diethylene glycol is the most efficient liquid medium when silicon powder is ground using a wet-milling process. The FT-IR results show that the Si-O band intensity in an unground silicon powder is quite strongbecause oxygen becomes incorporated with silicon to form $SiO_2$ in air. By applying deionized water as a liquid medium for the grinding of silicon, the $SiO_2$ content increased from 4.12% to 31.7%. However, in the cases of dehydrated ethanol and diethylene glycol, it was found that the $SiO_2$ contents after grinding only changed insignificantly, from 4.12% to 5.91% and 5.28%, respectively.

전자선 가교 방법을 이용한 탄소/탄화규소 복합재 제조 및 특성 (Fabrication and Characterization of C/SiC Composite by Electron Beam Curing)

  • 신진욱;전준표;강필현
    • 폴리머
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    • 제33권6호
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    • pp.575-580
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    • 2009
  • 폴리카보실란에 탄소직물을 보강제로 이용하여 제조한 탄소/탄화규소 복합재는 좋은 내산화 특성과 열 충격에 강한 특성으로 인해 높은 온도의 구조체에 적용되고 있다. 본 연구에서는 고분자 함침 열분해법을 이용하여 탄소직물에 폴리카보실란 용액을 함침한 후, 전자선을 이용하여 가교하고, 열분해 과정을 통해 탄소/탄화규소 복합재로 제조하였다. 실험 결과 복합재 시료의 공극률과 밀도는 각각 13.5%와 $2.44\;g/cm^3$을 나타냈고, 내산화 특성은 지속적인 고온의 산화 분위기에서 95.9%의 잔류량을 나타내어 본 연구에서 제조한 탄소/탄화규소 복합재의 우수한 내산화 특성을 확인하였다.