• 제목/요약/키워드: Glassy Carbon

검색결과 215건 처리시간 0.019초

대형강괴 주조공정 중 비금속개재물 저감연구 (Nonmetallic Inclusion in the Large Steel Ingot Casting Process)

  • 남궁정;김용찬;김문철;오상훈;김남수
    • 한국소성가공학회:학술대회논문집
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    • 한국소성가공학회 2008년도 춘계학술대회 논문집
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    • pp.52-56
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    • 2008
  • Inclusions in forged large steel ingots of plan carbon steel and tool steel are investigated using optical microscop observation and WDX analysis. The large nonmetallic inclusions which is over $30\sim300{\mu}m$ in their diameter were observed in the samples that has been no good on a nondestructive test. The most of the inclusions were consist of some kind of oxides, ${Al_2}{O_3}$, $SiO_2$, CaO, MgO in forms of particles and glassy with an iron particles. The experimental large steel ingot was cast with a pouring temperature which is about ten centigrade higher than the field standard. The inclusions were observed in the test ingot are the smaller than that was in a usual forged steel ingot and is spherical shape with a glassy agglomerated ${Al_2}{O_3}-SiO_2-CaO-MgO$ particle. The pouring temperature is affected on removing the nonmetallic inclusions during the solidification by a floating mechanism.

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Morphology of Metal Salt of Carboxylic Acid: Metal and Acid Dependency on Branched Round Cluster Images

  • Min Su Kang;Kwang-Jin Hwang
    • 대한화학회지
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    • 제67권4호
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    • pp.222-225
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    • 2023
  • Metallic salts of C10-18 aliphatic carboxylic acids were prepared and their scanning electron microscopic images were analyzed for the morphology dependency with the metal and the carboxylic acid. Regardless of metal ion, metal salts of dicarboxylic acids showed a high crystallinity with a fiber image (SuA-Na). The aromatic dicarboxylates also represented a morphology of a rectangular-rod or board shapes (IA-Li, IA-Ba). With Na ion, most aliphatic carboxylate (MA, PA, SA) showed a fiber-like crystallinity. However, other monovalent Li, K and multivalent Mg, especially Al ion resulted a glassy-amorphous in the metallic salts of acids (MA, PA, SA). With divalent Ba and Ca ions, the metal salt of aliphatic acids expressed a branched round cluster shape as in SA-Ca, SA-Ba. Both Li and Mg ions with a similar size showed a strong morphological similarity in the metallic salts of aliphatic acids MA, PA, SA. In the case of Na and Ca ions with a similar size (98, 106 pm), both ionic salts of stearic acid gave a branching effect for a fiber or round granular image. In the case of hydroxyl-aliphatic acids (HLA, HPA, HSA), the fiber images in HLA-Na and HSA-Na was appeared about 100 nm thicker than those of nonhydroxycarboxylates (LA-Na, SA-Na). The metallic salts of unsaturated C-18 carboxylic acids (OlA, LeA and LnA) showed an amorphous glassy image due to a kinked carbon chain.

카드뮴과 납 전기화학적 검출을 위한 전극선정에 관한 연구 (Study on Electrode Selection for Electrochemical Detection of Cadmium and Lead)

  • 김학진;김기영;모창연;조한근
    • Journal of Biosystems Engineering
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    • 제33권6호
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    • pp.404-409
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    • 2008
  • Excessive presence of heavy metals in environment affects plants and fruits grown in the contaminated area. Rapid on-site monitoring of heavy metals can provide useful information for efficiently characterizing heavy metal-contaminated sites and for minimizing the exposure of the contaminated food crops to humans. This study reports on the evaluation of gold and glassy carbon (GC) electrodes with mercury or bismuth as a coating material for simultaneous determination of cadmium (Cd) and lead (Pb) in 0.1 M $HNO_3$ solution by anodic stripping voltammetry (ASV). The use of a square-wave voltammetric potential between a working electrode and a reference electrode caused Cd and Pb ions deposited on the electrode surface to be oxidized, thereby generating electric currents at different potentials. The mercury-coated gold electrode was not sensitive enough to detect the usable range of Cd concentrations (1 to 100 ppb). The GC electrodes with mercury or bismuth displayed well-defined, sharp and separate current peaks for Cd and Pb ions when the square-wave voltammetric potentials were applied. The peak currents measured with both mercury- and bismuth- coated GC electrodes were linearly proportional to Cd and Pb concentrations in the range of 1 to 200 ppb in 0.1 M $HNO_3$ with strong linear relationships between concentration and peak current ($R^2$ > 0.95), indicating that both of Cd and Pb ions could be quantitatively measured.

네모파 산화전극벗김 전압전류법을 이용한 생체시료 중의 미량 수은 분석 (Determination of Trace Level Mercury in Bio-Materials by Square Wave Anodic Stripping Voltammetry)

  • 김일광;박성우;한종현;김윤근;천현자;박경옥
    • 대한화학회지
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    • 제37권5호
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    • pp.477-482
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    • 1993
  • 생체시료 중의 미량수은정량을 glassy carbon 전극을 사용하는 네모파 산화전극벗김 전압전류법으로 연구하였다. 생체시료는 분석에 들어가기 전에 질산과 황산 그리고 과망간산 칼륨으로 충분히 온침시켰다. 수은의 검출한계는 석출시간, 석출전위, pH, 그리고 저어줌속도 등에 의하여 크게 영향을 받았다. -1.0 volts에서 240초간 400rpm으로 저어주면서 수은을 석출하였을 때 검출한계는 $0.5\;ppb\;(2.5{\times}10^{-9} M)$이하였다. 이 방법은 분석시간이 짧고 감도가 높기 때문에 생체시료 중의 미량수은 분석에 유용하였다.

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Modified Glassy Carbon Electrode with Silver Nanoparticles/Polyaniline/Reduced Graphene Oxide Nanocomposite for the Simultaneous Determination of Biocompounds in Biological Fluids

  • Ghanbari, Kh.;Moloudi, M.;Bonyadi, S.
    • Journal of Electrochemical Science and Technology
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    • 제10권4호
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    • pp.361-372
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    • 2019
  • The silver nanoparticles/polyaniline/reduced graphene oxide nanocomposite modified glassy carbon electrode (Ag/PANI/RGO/GCE) was prepared by the electrochemical method. The Ag/PANI/RGO nanocomposite was characterized by transmission electron microscopy (TEM), field emission scanning electron microscopy (FE-SEM), Raman spectroscopy, X-ray diffraction (XRD), and electrochemical impedance spectroscopy (ESI). Two electrochemical techniques namely differential pulse voltammetry (DPV) and cyclic voltammetry (CV) were used to the electrochemical behaviors investigation of ascorbic acid (AA), dopamine (DA), and uric acid (UA). The Ag/PANI/RGO/GCE exhibited remarkable electrocatalytic activity towards the oxidation reaction of AA, DA, and UA in Britton-Robinson (BR) solution (pH=4.0). Under the optimal conditions, the determinations of AA, DA, and UA were accomplished using DPV. AA-DA and DA-UA peak potential separations were 130 and 180 mV, respectively. For simultaneous detection, the linear response ranges were in the two concentration ranges of 0.05-0.8 mM and 2.0-16.0 mM with detection limit 0.412 μM (S/N = 3) for AA, 0.7-90.0 μM and 90.0-1000.0 μM with detection limit 0.023 μM (S/N = 3) for DA, and 0.8-70.0 μM and 70.0-1000.0 μM with detection limit 0.050 μM (S/N = 3) for UA. This modified electrode showed good sensitivity, selectivity, and stability with applied to determine AA, DA, and UA in human urine and drug.

Green Synthesis of Platinum Nanoparticles by Electroreduction of a K2PtCl6 Solid-State Precursor and Its Electrocatalytic Effects on H2O2 Reduction

  • Kim, Kyung Tae;Jin, Sung-Ho;Chang, Seung-Cheol;Park, Deog-Su
    • Bulletin of the Korean Chemical Society
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    • 제34권12호
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    • pp.3835-3839
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    • 2013
  • A new synthesis route for Pt nanoparticles by direct electrochemical reduction of a solid-state Pt ion precursor ($K_2PtCl_6$) is demonstrated. Solid $K_2PtCl_6$-supported polyethyleneimine (PEI) coatings on the surface of glassy carbon electrode were prepared by simple mixing of solid $K_2PtCl_6$ into a 1.0% PEI solution. The potential cycling or a constant potential in a PBS (pH 7.4) medium were applied to reduce the solid $K_2PtCl_6$ precursor. The reduction of Pt(IV) began at around -0.2 V and the reduction potential was ca. -0.4 V. A steady state current was achieved after 10 potential cycling scans, indicating that continuous formation of Pt nanoparticles by electrochemical reduction occurred for up to 10 cycles. After applying the reduction potential of -0.6 V for 300 s, Pt nanoparticles with diameters ranging from $0.02-0.5{\mu}m$ were observed, with an even distribution over the entire glassy carbon electrode surface. Characteristics of the Pt nanoparticles, including their performance in electrochemical reduction of $H_2O_2$ are examined. A distinct reduction peak observed at about -0.20 V was due to the electrocatalytic reduction of $H_2O_2$ by Pt nanoparticles. From the calibration plot, the linear range for $H_2O_2$ detection was 0.1-2.0 mM and the detection limit for $H_2O_2$ was found to be 0.05 mM.

유리질 탄소전극에서 양극벗김 네모파 전압-전류법에 의한 생체내 미량 수은의 정량 (Determination of Bio-Accumulated Trace Mercury by Anodic Stripping Square Wave Voltammetry at Glassy Carbon Electrode)

  • 김일광;천현자;정승일;백승화;한완수
    • 대한화학회지
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    • 제45권4호
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    • pp.298-303
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    • 2001
  • 생체시료에 함유된 미량수은을 유리질 탄소전극을 사용하는 양극 벗김 네모파 전압-전류법으로 정량하였다. 생체시료는 HNO3/H2SO4 산혼합용액으로 삭히고, KMnO4를 가하여 산화시켰다. 수은의 검출한계는 석출전위, 시 간, pH, 그리고 용액을 저어주는 속도 등에 크게 영향을 받았다. 1.0 volts vs. Ag/AgCl에서 400rpm으로 저어주면서 240 sec 동안 석출시켰을 경우, 검출한계는 0.5 ppb 이하였다. 흰쥐에 대한 수은의 생체 축적량은 신장과 간에서 높았고, 뇌에서는 매우 낮았다.

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Nafion-ethylenediamine이 수식된 유리탄소전극에 의한 시차펄스전압전류법으로 철(II) 이온의 정량 (Differential Pulse Voltammetric Determination of Iron(II) ion with a Nafion-Ethylenediamine Modified Glassy Carbon Electrode)

  • 김경원;김희철;김성현;박병호;김연희;김경남;고영춘
    • 대한화학회지
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    • 제47권2호
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    • pp.115-120
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    • 2003
  • Perfluorinated sulfonated polymer(Nafion)-ethylenediamine(en)이 화학수식된 유리탄소전극으로 Fe(II) 이온의 정량에 대해 연구하였다. Fe(II) 이온의 착화제인 en을 nafion에 고정시켜 유리탄소전극 표면에 수식하면 이 수식전극의 en은 Fe(II) 이온과 $[Fe(en)_3]^{+2}$의 착물을 형성한다. Nafion-en이 화학수식된 유리탄소전극에서 시차펄스전압전류법에 의한 Fe(II) 이온의 산화봉우리전위는 0.340${\pm}$0.015 V(vs. Ag/AgCl), 측정범위는 $5{\times}10^{-6}{\sim}0.2{\times}10^{-3} M(0.28{\sim}11.17 mg/L)$, 검출한계(3s)는 $1.89{\times}10^{-5}$M(1.056 mg/L)이었다.

Nanostructured Metal Organic Framework Modified Glassy Carbon Electrode as a High Efficient Non-Enzymatic Amperometric Sensor for Electrochemical Detection of H2O2

  • Naseri, Maryam;Fotouhi, Lida;Ehsani, Ali
    • Journal of Electrochemical Science and Technology
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    • 제9권1호
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    • pp.28-36
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    • 2018
  • Metal-organic frameworks have recently been considered very promising modifiers in electrochemical analysis due to their unique characteristics among which tunable pore sizes, crystalline ordered structures, large surface areas and chemical tenability are worth noting. In the present research, $Cu(btec)_{0.5}DMF$ was electrodeposited on the surface of glassy carbon electrode at room temperature under cathodic potential and was initially used as the active materials for the detection of $H_2O_2$. The cyclic voltammogram of $Cu(btec)_{0.5}DMF$ modified GC electrode shows distinct redox peaks potentials at +0.002 and +0.212 V in 0.1 M phosphate buffer solution (pH 6.5) corresponding to $Cu^{(II)}/Cu^{(I)}$ in $Cu(btec)_{0.5}DMF$. Acting as the electrode materials of a non-enzymatic $H_2O_2$ biosensor, the $Cu(btec)_{0.5}DMF$ brings about a promising electrocatalytic performance. The high electrocatalytic activity of the $Cu(btec)_{0.5}DMF$ modified GC electrode is demonstrated by the amperometric response towards $H_2O_2$ reduction with a wide linear range from $5{\mu}M$ to $8000{\mu}M$, a low detection limit of $0.865{\mu}M$, good stability and high selectivity at an applied potential of -0.2 V, which was higher than some $H_2O_2$ biosensors.

Electrochemical Determination of Dopamine Based on Carbon Nanotube-Sol-Gel Titania-Nafion Composite Film Modified Electrode

  • Park, Ji-Ae;Kim, Byung-Kun;Choi, Han-Nim;Lee, Won-Yong
    • Bulletin of the Korean Chemical Society
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    • 제31권11호
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    • pp.3123-3127
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    • 2010
  • A highly sensitive electrochemical detection method for dopamine (DA) has been developed by relying on a multiwalled carbon nanotube (CNT)-sol-gel titania-Nafion composite film modified glassy carbon (GC) electrode. The CNT-titania-Nafion/GC electrode exhibited excellent electrocatalytic activity towards DA. Therefore, the CNT-titania-Nafion/GC electrode showed improved voltammetric and amperometric responses for DA compared to those obtained with both titania-Nafion/GC and Nafion/GC electrodes. The CNT-titania-Nafion/GC electrode gave a linear response ($R^2$ = 0.999) for DA from $0.5\;{\mu}M$ to 0.5 mM with a detection limit (S/N = 3) of $0.1\;{\mu}M$ and a good sensitivity of 150 mA/M while other electrodes such as CNT-Nafion/GC, titania-Nafion/GC, and a bare GC gave a sensitivity of 89, 39, and 36 mA/M, respectively. Besides, the CNT-titania-Nafion/GC electrode displayed very fast response time within 2 s. The modified electrode showed good selectivity against ascorbic acid. The modified electrode showed good stability and reproducibility. The CNT-titania-Nafion/GC electrode was applied to the determination of DA in urine and serum samples.