• 제목/요약/키워드: Ion gel

검색결과 793건 처리시간 0.024초

PHOTOCATALYTIC DEGRADATION OF 2-CHLOROPHENOL USING TiO₂THIN FILMS PREPARED BY CHEMICAL VAPOR DEPOSITION AND ION BEAM SPUTTERING METHOD

  • Jung, Oh-Jin;Kim, Sam-Hyeok;Jo, Ji-Eun;Hwang, Chul-Ho
    • Environmental Engineering Research
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    • 제7권4호
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    • pp.227-237
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    • 2002
  • Chemical vapor deposition (CVD), ion beam sputtering (IBS) and sol-gel method were used to prepare TiO$_2$ thin films for degradation of hazardous organic compounds exemplified by 2-chlorophenol (2-CP). The influence of supporting materials and coating methods on the photocatalytic activity of the TiO$_2$ thin films were also studied. TiO$_2$ thin films were coated onto various supporting materials including steel cloth (SS), copper cloth, quartz glass tube (QGT), and silica gel (SG). Results indicate that SS (37 μm)- TiO$_2$ thin film prepared by IBS method improves the photodegradation of 2-CP. Among all supporting materials studied, SS(37 μm) is found to be the best support.

Purification and Characterization of a Collagenolytic Protease from the Filefish, Novoden modestrus

  • Kim, Se-Kwon;Park, Pyo-Jam;Kim, Jong-Bae;Shahidi, Fereidoon
    • BMB Reports
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    • 제35권2호
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    • pp.165-171
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    • 2002
  • A serine collagenolytic protease was purified from the internal organs of filefish Novoden modestrus, by ammonium sulfate, ion-exchange chromatography on a DEAE-Sephadex A-50, ion-exchange rechromatography on a DEAE-Sephadex A-50, and gel filtration on a Sephadex G-150 column. The molecular mass of the filefish serine collagenase was estimated to be 27.0 kDa by gel filtration and SDS-PAGE. The purified collagenase was optimally active at pH 7.0-8.0 and $55^{\circ}C$. The purified enzyme was rich in Ala, Ser, Leu, and Ile, but poor in Trp, Pro, Tyr, and Met. In addition, the purified collagenolytic enzyme was strongly inhibited by N-P-toluenesulfonyl-L-lysine chloromethyl ketone (TLCK), diisopropylfluorophosphate (DFP), and soybean trypsin inhibitor.

Pseudomonas fluorescens에 의한 Furfural의 분해대사 조절물질에 관하여 (Purification and Characterization of the Regulatory Substance of Furfural Biodegradation in Pseudomonas fluorescens)

  • 이병웅;유병설;이계준;하영칠
    • 미생물학회지
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    • 제23권4호
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    • pp.241-247
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    • 1985
  • Pseudomonas fluorescens에 의해 세포외에 생산된 furfural의 furoic acid로의 생물학적 전환을 촉진시키는 ninhydrin 반응에 양성인 대사물 (Ninhydrin positive Substance=NPS)을 ion exchange chromatography와 gel permeation chromatography 그리고 cellulose columm chromatography에 의하여 분리, 정제하였다. IR spectrophotometry와 $^H$-NMR spectrometry 그리고 $^{13}C-NMR$ spectrometry에 의해 이 NPS는 -$^H$ and $-NH_2$와 그리고 $-CH_2-OH$group을 갖는 유기물질로 추정된다.

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능이버섯으로부터 Fibrin 분해활성이 있는 단백질의 분리 및 정제 (Isolation and Purification of Fibrinolytic Enzyme of Edible Mushroom, Sarcodon aspratus(Berk.)S. Ito)

  • 이종호;양정례;정청송;김희숙;조재선
    • 생명과학회지
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    • 제11권6호
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    • pp.561-567
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    • 2001
  • 능이버섯[Sarcodon aspratus(Berk.)S.Ito]의 fibrin 분해 활성물질을 분리정제하기 위하여(N $H_4$)$_2$S $O_4$침전법, DE52 anion exchange column chromatography, Sephacryl-S2000 gel filtration chromatography 및 Mono S cation FPLC를 행하였으며 정제된 효소의 특성을 측정하였다. 혈전용해 요소의 활성물질은 DE52 anion exchange colum chroma-tography에 NaCI의 농도가 0.2M 정도에서 용출되었으며 계속된 Sephacryl-S200 gel fitration chromatography 및 Mono S cation EPLC를 실시한 결과 단일 Peak를 얻었고 혈전용해효소의 특이활성은 55.2 U/mg protein으로 조효소액으로 비하여 11.3 배 증가하였으며 수율은 49.5%이었다. 또한 Mono S cation EPLC에서 얻은 활성획분을 12% SDS-PAGE로 전기영동한 결과 단일 band를 얻었으며 gel filtration의 결과와 비교함으로서 정제된 능이의 혈전용해 효소의 분자량은 29.300 Da인 것으로 확인되었다. 능이로 부터 정제한 혈전용해효소는 pH가 높아질수록 효소활성이 증가하였으며 pH 10.5의 알카리성에서도 안정하였으며 6$0^{\circ}C$이상의 온도에서는 효소활성이 급격히 실활하기 시작하였지만 8$0^{\circ}C$에서 25%의 상대활성을 보였다. 또한 본 효소는 C $u^{2+}$이온 $Co^{3+}$ 이온 등 중금속에 의하여 68%및 38%활성이 저해되었으며 $Ca^{2+}$이온 또는 $Mg^{2+}$의 초딤색 인 EDTA및 serine protease inhibitor이 PMSF에 의하여 활성이 저해되었었다. 이러한 결과들은 능이의 혈전용해효소가 Ca.sup 2+/또는M $g^{2+}$에 의하여 활성이 증가하는 serine protease임을 암시해 주고 있다.

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졸-겔 방법에 의한 전기적 착색 박막의 제작과 특성 (PREPARATION AND PROPERTIES OF EIECTROCHROMIC WINDOW COATING BY THE SOL-GEL METHOD)

  • 이길동
    • 태양에너지
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    • 제12권2호
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    • pp.18-27
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    • 1992
  • 졸-겔 기술에 의해 $WO_3$ 다충박막이 유리와 ITO coated glass 위에 증착되었다. 특성은 XRD, 분광광도계, DTA/TGA, SEM/EDAX 그리고 RBS에 의해서 분석되었다. 균질한 $WO_3$막은 유리기판위에 dipping속도 5mm/s에서 증착 되었으며 이 시료는 희석된 HCI 전해액을 사용하여 착색시킨 결과 낮은 근적외선 투과율을 나타내었다. DTA 결과 $380^{\circ}C{\sim}500^{\circ}C$ 범위의 gel data는 $WO_3$의 결정화 온도 형성을 결정하였으며 이 측정치는 졸-겔 박막의 결정화 온도와 일치하였다. RBS에 의해 착색되지 않은 $WO_3$ 졸-겔 막의 화학조성은 $WO_3$였다.

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BaTiO3 습식직접합성 반응기구에 관한 연구 (Reaction Mechanism on the Synthesis of BaTiO3 by Direct Wet Process)

  • 이경희;이병하;김대웅
    • 한국세라믹학회지
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    • 제26권3호
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    • pp.371-380
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    • 1989
  • The purpose of this experiment is to elucidate the reaction mechanism concerning to the formation of crystalline BaTiO3 synthesized by adding the pH control agent(KOH soln) in TiCl4 and BaCl2 solution (Wet direct synthetic method). In this expeirment, it is identified that the amorphous barium-titanate having Ba-O-Ti bonding is formed above pH5 due to the -OH- ion and Ti-gel is formed below pH5 due to the polymerization of metatitanic acid. The bonding of the amorphous Ba-O-Ti is identified by FT-IR spectrum and crystallization temperature is about 82$0^{\circ}C$. If the pH of the above system according to the -OH- ion concentration is above 13.8, the polymerized metatitanic acid will be depolymerized and produce [TiO3]2+ion and crystalline BaTiO3 is formed by reacting the produced [TiO3]-- ion with the active Ba++ ion.

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Cycling Performance of Li4Ti5O12 Electrodes in Ionic Liquid-Based Gel Polymer Electrolytes

  • Kim, Jin-Hee;Kang, Yong-Ku;Kim, Dong-Won
    • Bulletin of the Korean Chemical Society
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    • 제33권2호
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    • pp.608-612
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    • 2012
  • We investigated the cycling behavior of $Li_4Ti_5O_{12}$ electrode in a cross-linked gel polymer electrolyte based on non-flammable ionic liquid consisting of 1-butyl-1-methylpyrrolidinium bis(trifluoromethanesulfonyl) imide and vinylene carbonate. The $Li_4Ti_5O_{12}$ electrodes in ionic liquid-based gel polymer electrolytes exhibited reversible cycling behavior with good capacity retention. Cycling data and electrochemical impedance spectroscopy analyses revealed that the optimum content of the cross-linking agent necessary to ensure both acceptable initial discharge capacity and good capacity retention was about 8 wt %.

Electrochemical Properties of Cross-linked Polyurethane Acrylate-Based Gel Polymer Electrolyte

  • Kim, Hyun-Soo;Kim, Sung-Il;Choi, Gwan-Young;Moon, Seong-In;Kim, Sang-Pil
    • 전기화학회지
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    • 제5권4호
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    • pp.197-201
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    • 2002
  • In this study, a gel polymer electrolyte was prepared from urethane acrylate and its electrochemical performances were evaluated. And, $LiCoO_2/GPE/graphite$ cells were prepared and their performances depending on discharge currents and temperatures were evaluated. The precursor containing $5 vol\%$ curable mixture had a low viscosity relatively. Ionic conductivity of the gel polymer electrolyte at room temperature and $-20^{\circ}C$ was ca. $5.9\times10^{-3}S{\cdot}cm^{-1}\;and\;1.7\times10^{-3}S{\cdot}cm^{-1}$, respectively. GPE showed electrochemical stability up to potential of 4.5V vs. $Li/Li^+.LiCoO_2/GPE/graphite$ cell showed a good high-rate and a low-temperature performance.

전해질 첨가에 따른 키토산/Sodium Dodecyl Sulfate 상호작용의 변화 (The Change of Interactions of Chitosan/Sodium Dodecyl Sulfate in the Presence of Electrolytes)

  • 배현숙;강인숙
    • 한국의류학회지
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    • 제27권5호
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    • pp.523-523
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    • 2003
  • The change of interactions of anionic surfactants, sodium dodecyl sulfate(SDS) and sodium tetradecyl sulfate(575) in the presence of electrolytes, to the chitosan-based polyelectrolyte(sol'n and gel phase) were studied. The chitosan gel used in this study were crosslinked with epichlorohydrin(ECH). Binding isotherms were determined by potentiometric technique using a surfactant ion selective solid-state electrode and the results were represented by using the sequence generating function(SGF) method. The results of binding isotherm were shown comparatively high cooperativity. The addition of electrolytes in the chitosan/SDS system resulted in a shift of the binding to higher free surfactant concentration because of screen effect by the electrolytes. Degree of binding of chitosan gel was higher than that of chitosan sol'n. And also a conformational phase transition of the chitosan gel in the presence of electrolytes has been investigated.

전해질 첨가에 따른 키토산/Sodium Dodecyl Sulfate 상호작용의 변화 (The Change of Interactions of Chitosan/Sodium Dodecyl Sulfate in the Presence of Electrolytes)

  • 배현숙;강인숙
    • 한국의류학회지
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    • 제27권5호
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    • pp.524-532
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    • 2003
  • The change of interactions of anionic surfactants, sodium dodecyl sulfate(SDS) and sodium tetradecyl sulfate(575) in the presence of electrolytes, to the chitosan-based polyelectrolyte(sol'n and gel phase) were studied. The chitosan gel used in this study were crosslinked with epichlorohydrin(ECH). Binding isotherms were determined by potentiometric technique using a surfactant ion selective solid-state electrode and the results were represented by using the sequence generating function(SGF) method. The results of binding isotherm were shown comparatively high cooperativity. The addition of electrolytes in the chitosan/SDS system resulted in a shift of the binding to higher free surfactant concentration because of screen effect by the electrolytes. Degree of binding of chitosan gel was higher than that of chitosan sol'n. And also a conformational phase transition of the chitosan gel in the presence of electrolytes has been investigated.