• 제목/요약/키워드: radical distribution

검색결과 203건 처리시간 0.026초

Effect of Freeze-Drying and Hot Air-Convection Drying on the Antioxidative Activity of Butterbur (Petasites japonicus)

  • Cheong, Sun-Hee;Kim, Mi-Yeon;Son, Chan-Wok;Kim, Min-Hee;Lee, Yun-Jin;Kim, Mee-Ree
    • Food Quality and Culture
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    • 제2권2호
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    • pp.61-66
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    • 2008
  • The principal objective of this study was to assess the anti oxidative activities of Petasites japonicus against oxidative stress in bovine brain tissue. Petasites japonicus is found with a relatively widespread distribution, and is cultivated as a culinary vegetable in Korea. Petasites japonicus samples were dried either by freeze-drying or by hot air-convection drying ($80^{\circ}C$), then evaluated for their anti oxidative activity by measuring 1-dipheny-1,2-picrylhydrazyl (DPPH) radical scavenging, and by measuring thiobarbituric acid-reactive substances (TBARS) in brain homogenates subjected to $Fe^{2+}$-mediated lipids with or without the addition of botanical extract. Hot air convection-drying resulted in a slight increase in the extraction yield as compared with freeze-drying. However, total phenol and flavonoid contents in freeze-dried Petasites japonicas were significantly higher than those of hot air convection-drying. Freeze-drying increased the free radical scavenging activity of Petasites japonicas, leaves, and stems by 52.6, 28.6, and 248.0%, as compared with hot air convection-drying. Additionally, the $IC_{50}$ values measured by TBARS in hot air convection-dried Petasites japonicas, leaves, and stems were increased by 36.0, 31.6, and 15.9%, as compared to those of freeze-drying. Although anti oxidative activity was reduced slightly by heat processing in Petasites japonicas, freeze-drying for each portion of Petasites japonicus was the most appropriate for use as a functional food and pharmaceutical material.

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비정상 소화 과정에서의 화염 온도 및 OH 라디칼의 변화 (Changes of the Flame Temperature and OH Radical in the Unsteady Extinction Process)

  • 이은도;이기호;오광철;신현동
    • 대한기계학회논문집B
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    • 제28권12호
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    • pp.1557-1566
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    • 2004
  • A flame extinction phenomenon is a typical unsteady process in combustion. Flame extinction is characterized by various physical phenomena, such as convection, diffusion, and the production of heat and mass. Flame extinction can be achieved by either increasing the strain rate or curvature, by diluting an inert gas or inhibitor, or by increasing the thermal or radiant energy loss. Though the extinction is an inherently transient process, steady and quasi-steady approaches have been used as useful tools for understanding the flame extinction phenomenon. Recently, unsteady characteristics of flames have been studied by many researchers, and various attempts have been made to understand unsteady flame behavior, by using various extinction processes. Representative parameters for describing flame, such as flame temperature, important species related to reactions, and chemi-luminescence of the flame have been used as criterions of flame extinction. In these works, verification of each parameter and establishing the proper criterions of the extinction has been very important. In this study, a time-dependent flame temperature and an OH radical concentration were measured using optical methods, and the instantaneous change of the flame luminosity was also measured using a high-speed ICCD (HICCD) camera. We compare the unsteady extinction points obtained by three different methods, and we discuss transient characteristics of maximum flame temperature and OH radical distribution near the extinction limit.

리빙라디칼 중합법을 포함한 화학적 방법에 의한 고무의 개질 (Modification of Rubbers through Chemical Reactions including Controlled/"living" Radical Polymerization Techniques)

  • 주상일;조현철;이상훈;홍성철
    • Elastomers and Composites
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    • 제44권2호
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    • pp.122-133
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    • 2009
  • 고무는 천연 고무를 비롯하여 부타디엔 고무, 스티렌-부타디엔 고무, 니트릴-부타디엔 고무, EPDM, 염소화 고무 등 산업적 요구에 따라 발전하여 왔다. 광범위한 분야에서 고무가 사용됨에 따라 새로운 물성을 갖는 합성 고무나 개질 고무의 생산이 필요하게 되었다. 본 리뷰 논문에서는 이중 결합을 포함하는 고무의 화학적 개질을 통하여 고무의 구조를 변화시키거나, 관능기, 이종 고분자 등을 도입하는 몇 가지 방법들에 대하여 정리해 보고자 한다. 특히, 최근에 많은 응용이 시도되고 있는 리빙 라디칼 중합법에 의한 고무의 개질을 소개하고 이의 효과를 알아보고자 한다.

바이오디젤 및 바이오디젤 혼합 연료의 산화 특성 I (Oxidation Characteristics of Biodiesel and Its Blend Fuel I)

  • 정충섭;동종인
    • 공업화학
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    • 제18권3호
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    • pp.284-290
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    • 2007
  • 대두유로부터 생산된 바이오디젤과 바이오디젤 혼합 연료유를 대상으로 산화 특성과 지방산메틸에스터 함량 등 화학적 분석을 수행하여 자동차용 연료로서의 품질특성을 파악하였다. 대두유로부터 생산된 바이오디젤은 불포화 지방산인 oleic acid, linoleic acid 및 linolenic acid가 85 wt% 이상 함유되어 있었다. 특히 활성 메틸렌기를 함유한 다불포화 지방산인 linoleic acid와 linolenic acid가 60 wt% 이상 함유되어 있어 상대적으로 자동산화가 쉽게 일어나는 것으로 판단된다. 산화반응시 주요 반응물질은 linoleic acid와 linolenic acid였으며, 이들의 라디칼 자동산화에 의해서 비점이 약 $500^{\circ}C$ 전 후에 있는 탄소수 36 전 후의 고분자 물질이 형성되는 것을 확인하였다

Preparation of Ag/PVP Nanocomposites as a Solid Precursor for Silver Nanocolloids Solution

  • Hong, Hyun-Ki;Park, Chan-Kyo;Gong, Myoung-Seon
    • Bulletin of the Korean Chemical Society
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    • 제31권5호
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    • pp.1252-1256
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    • 2010
  • A polyvinylpyrrolidone (PVP)/Ag nanocomposites was prepared by the simultaneous thermal reduction and radical polymerization route. The in situ synthesis of the Ag/PVP nanocomposites is based on the finding that the silver n-propylcarbamate (Ag-PCB) complex can be directly dissolved in the NVP monomer, and decomposed by only heat treatment in the range of 110 to $130^{\circ}C$ to form silver metal. Silver nanoparticles with a narrow size distribution (5 - 40 nm) were obtained, which were well dispersed in the PVP matrix. A successful synthesis of Ag/PVP nanocomposites then proceeded upon heat treatment as low as $110^{\circ}C$. Moreover, important advantages of the in situ synthesis of Ag/PVP composites include that no additives (e.g. solvent, surface-active agent, or reductant of metallic ions) are used, and that the stable silver nanocolloid solution can be directly prepared in high concentration simply by dissolving the Ag/PVP nanocomposites in water or organic solvent.

곁가지에 다양한 길이의 알코올 그룹을 지닌 고분자들의 저임계 용액온도 민감성 제어 (Precise Control of Thermoresponsive Properties of Polymers with Hydroxy Groups in the Side Chains)

  • 이형일
    • 폴리머
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    • 제39권1호
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    • pp.165-168
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    • 2015
  • 하이드록시 그룹을 지닌 온도민감형 고분자들이 원자전이라디칼중합법(ATRP)과 클릭반응(click reaction)에 의해 합성되어졌다. 고분자들의 분자량과 분자량 분포도는 gel permeation chromatography(GPC)에 의하여 얻어졌고, 고분자들의 분자량은 잘 제어되었으며 분자량 분포도도 낮게 유지되었다. 클릭반응의 효율은 $^1H$ NMR spectroscopy에 의해 얻어졌으며, 높은 효율을 나타내었다. 고분자 사슬 곁가지의 아민 그룹의 종류와, 치환된 알코올 그룹의 종류에 따라 저임계 용액 온도(LCST)의 제어가 가능했다.

Synthesis of High Molecular Weight 3-Arm Star PMMA by ARGET ATRP

  • Jeon, Hyun-Jeong;Youk, Ji-Ho;Ahn, Sung-Hee;Choi, Jin-Hwan;Cho, Kwang-Soo
    • Macromolecular Research
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    • 제17권4호
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    • pp.240-244
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    • 2009
  • High molecular weight(MW), 3-arm star poly(methyl methacrylate)(PMMA) with a narrow MW distribution($M_n$=570,000 g/mol, PDI=1.36) was successfully synthesized by activators regenerated by electron transfer(ARGET) atom transfer radical polymerization(ATRP). The polymerization was carried out with a trifunctional initiator/$CuBr_2$/N,N,N',N",N"-pentamethyldiethy lenetriamine(PMDETA) initiator/catalyst system in the presence of a tin(II) 2-ethylhexanoate [$Sn(EH)_2$] reducing agent at $90^{\circ}C$. The concentration of the copper catalyst was as low as 30 ppm, and a high initiation efficiency of the initiating sites was obtained. The chain-end functionality of the high MW, 3-arm star PMMA was confirmed by a chain extension experiment with styrene via ARGET ATRP, using the same catalyst system.

산소부화공기가 동축 비예혼합 제트의 연소특성에 미치는 영향 (II) - 화염의 구조와 온도분포 - (Effect of Oxygen Enriched Air on the Combustion Characteristics in a Coaxial Non-Premixed Jet (II) - Flame Structure and Temperature Distribution -)

  • 곽지현;전충환;장영준
    • 대한기계학회논문집B
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    • 제28권2호
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    • pp.223-229
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    • 2004
  • Combustion using oxygen enriched air is known as a technology which can increase thermal efficiency due to increase of the flame temperature. Flame shapes, schlieren photos, OH radical chemiluminescence and local flame temperature were examined as a function of OEC(Oxygen Enriched Concentration) in a coaxial non-premixed jet. With increase of OEC, flame length and width decreased, but its brightness increased significantly, and the size of vortices in the flame also increased. Especially, the reaction around the flame surface became active. The strong OH intensity appeared to be made and moved from middle stream to upper one with increase of OEC, which shows combustion reaction in the upper stream becomes more dominant In addition, the temperature distributions of the flames showed similar tendency with OH radical intensities. A flame with high temperature and strong stability was obtained with increasing OEC of the coflow.

DFWM(degenerate four wave mixing)을 이용한 대향류버너 화염내의 OH 라디칼 스펙트럼 측정 (Measurement of OH radical spectrum in counterflow burner using degenerate four wave mixing)

  • 이은성;한재원
    • 한국광학회지
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    • 제7권2호
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    • pp.142-149
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    • 1996
  • 대향류버너의 화염에서 연소반응의 중간단계 생성물로 존재하는 OH라디칼의 축퇴 4광자 혼합스팩트럼을 비포화영역에서 Forward Box 형태의 위상정합조건으로 측정하였다. X$^{2}$.PI..rarw.A$^{2}$.SIGMA.$^{+}$ 천이선들 중 R$_{1}$-가지 분광선들의 세기로부터 회전에너지 준위의 밀도분포를 구하고 볼쯔만분포와 비교하여 온도를 구하였다. 흡수분광스펙트럼을 측정하여 화염내에서 레이저의 흡수효과를 보정하여 주었다. 측정된 온도의 오차는 2000K 근방에서 .+-.60K로서 CARS로 얻은 온도와 오차범위내에서 일치하였다. 화염의 여러부분에서 스펙트럼을 측정하여 온도분포와 OH농도분포를 얻었다.

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Hyperthermal Collision-induced Dissociation of Bromotoluene Radical Cations at Self-Assembled Monolayer Surfaces

  • Jo, Sung-Chan;Augusti, Rodinei;Cooks, R. Graham
    • Mass Spectrometry Letters
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    • 제2권1호
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    • pp.24-27
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    • 2011
  • Hyperthermal ion/surface collisions of bromotoluene radical cations were studied using perfluorinated (F-SAM) and hydroxyl-terminated (OH-SAM) self-assembled monolayer surfaces in a tandem mass spectrometer with BEEQ geometry. The isomers were differentiated by ion abundance ratios taken from surface-induced dissociation (SID). The dissociation rate followed the order of ortho > meta > para isomers. The peak abundance ratio of m/z 51 to m/z 65 showed the best result to discern the isomers. A dissociation channel leading to tolylium ion was suggested to be responsible for the pronounced isomeric differences. The capability of SID to provide high-energy activation with narrow internal energy distribution may have channeled the reaction into the specific dissociation pathway, also facilitating small differences in reaction rates to be effective in the spectral time window of this experiment. All of the molecular ions experiencing reactive collisions with the F-SAM surface undergo transhalogenation, in which a fluorine atom on the surface replaces the bromine in the incoming ions. This reactive collision was dependent on the laboratory collision energy occurring in ca. 40.75 eV range.