• Title/Summary/Keyword: 이온확산

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The Enhancement Effect of the Electrochemical Deposition in the Recovering Process of Cu from CuSO4 Solution (황산구리 용액으로부터의 구리회수공정에서 초음파에 의한 전착반응의 증대효과)

  • Yoon, Yong-Soo;Hong, In-Kwon;Lee, Jae-Dong;Jeong, Il-Hyun
    • Applied Chemistry for Engineering
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    • v.5 no.2
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    • pp.199-208
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    • 1994
  • In this study, the ultrasound which provides the properties of mixing, and surface cleaning effect, the increase of the effective reaction surface area and the enhancement of the effective collision frequency, was used to enhance the recovering efficiency of Cu from the Cu-ion containning waste water. The ultrasonic reactor used in this study was designed and constructed for improving the disadvantage of the existing ultrasonic reactor. From the experimental result and its analysis, we obtained following conclusions. 1. The ultrasound increased the rate of electrochemical deposition to 582.2% in maximum at the condition of $0.1M-CuSO_4$, and 2.1 V-overpotential. 2. The enhancement effect of ultrasound induced by the reduction of diffusion layer thickness was 277.8% in maximum and induced by the other effect except for the reduction effect of the diffusion layer thickness was 253.6% in maximum at $0.1M-CuSO_4$ and 2.1V overpotential. 3. This study gave the possibility of the scale-up of ultrasonic reactor and in particular, ultrasonic reactor would be effective in the treatment of waste water containning a low concentration of Cu ion.

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Enhanced size uniformity and dispersibility of BaTiO3 nanoparticles by hydrothermal synthesis (균일성과 분산성이 향산된 BaTiO3 나노입자의 수열합성)

  • Cho, Hoyeon;Park, Byoungnam
    • Journal of the Korean Crystal Growth and Crystal Technology
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    • v.30 no.3
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    • pp.91-95
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    • 2020
  • In this study, we report a hydrothermal synthesis in which BaTiO3 nanoparticles (NPs) with enhanced size uniformity and dispersibility are synthesized by increased time and temperature, increasing nucleation and diffusion rates. The formation process of an uniform size of 20 nm BaTiO3 NPs, which has not been extensively researched, was optimized through hydrothermal synthesis at 180℃. Simultaneous increase in the nucleation rate of TiO2 and diffusion length of Ba2+ ions, resulting from a higher temperature, allowed for the synthesis of BaTiO3 NPs (20 nm) with significantly enhanced size-uniformity. The size and crystallinity of BaTiO3 NPs which exhibit excellent dispersibility in hexane solvent were investigated using transmission electron microscopy and X-ray diffraction. The results presented herein provide insights into improving the size uniformity and dispersibility of BaTiO3 NPs by hydrothermal synthesis for applications to variety of electronic devices.

Synthesis of Tridentate-Schiff Base Co(II) Complexes and Their Electrochemical Properties (세자리 Schiff Base Co(Ⅱ) 착물의 합성과 전기화학적 성질)

  • Chae, Hui Nam;Choe, Yong Guk
    • Journal of the Korean Chemical Society
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    • v.42 no.4
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    • pp.422-431
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    • 1998
  • Tridentate Schiff base ligands such as $SIPH_2,\;SIPCH_2,\;HNIPH_2,\;and\; HNIPCH_2$ were prepared by the reaction of salicylaldehyde and 2-hydroxy-l-naphthaldehyde with 2-aminophenol and 2-amino-p-cresol. The structures and properties of ligands and their Co(II) complexes were investigated by elemental analysis, $^1H$NMR, IR, UV-visible spectra, and thermogravimetric analysis. The molar ratio of Schiff base to the metal of complexes was found to be 1:1. Co(II) complexes were contemplated to be hexa-coordinated octahedral configuration containing three water molecules. The redox process of ligands and complexes in DMSO solution containing 0.1 M TBAP as a supporting electrolyte were investigated by cyclic voltammetry with glassy carbon electrode. The redox process of the tridentate Schiff base ligands was totally irreversible. The redox process of Co(II) complexes were irreversible and one electron processes by two steps in diffusion controlled reaction. The reduction potential of the Co(II) complexes was shifted to the positive direction in the order [Co(Ⅱ)$(HNIPC)(H_2O)_3$]>[Co(Ⅱ)$(HNIP)(H_2O)_3$]>[Co(II)$(SIPC)(H_2O)_3$]>[Co(Ⅱ)$(SIP)(H_2O)_3], and their dependence on ligands were not so high.

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Electrochemical Behavior of Dissolved Hydrogen and Hydrogen Peroxide in Boric Acid Solution at the Elevated Temperature (붕산수용액 매질에서 용존수소와 과산화수소의 고온 전기화학 거동연구)

  • Yeon Jei-Won;Woo Seung-Kyun;Choi Young-Ku;Jung Yongju;Kim Won-Ho
    • Journal of the Korean Electrochemical Society
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    • v.7 no.1
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    • pp.21-25
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    • 2004
  • The electrochemical behaviors of dissolved hydrogen and hydrogen peroxide at a platinum disk electrode were investigated in boric acid solution by potentiostatic polarization method at the temperature of 25 and $200^{\circ}C$. The oxidation of dissolved hydrogen at $25^{\circ}C$ was kinetically controlled reaction, the rate of which depends upon the electron transfer on the electrode surface. As temperature was raised, however, the electrochemical characteristics of dissolved hydrogen were changed from a kinetically controlled reaction to a diffusion controlled one. One notable feature, with dissolved hydrogen at high temperature, is that an abnormal potential range was observed, where the oxidation rate of dissolved hydrogen rapidly decreased just before starting potential of water oxidation. We think it is caused by the deactivation of the electrode that results from the adsorption of hydroxyl ion on the surface of the platinum disk. On the contrary, a definite change with temperature was not identified in the case of the hydrogen peroxide except for the increase in current density that was due to the increasing diffusion coefcient with an increase of temperature.

Synthesis of Transition Metal Cu(II) Complexes and Their Electrochemical Properties (Cu(II) 전이금속 착물의 합성과 전기화학적 성질에 관한 연구)

  • Chae, Hee-nam;Choi, Yong-kook
    • Applied Chemistry for Engineering
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    • v.9 no.5
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    • pp.719-725
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    • 1998
  • Tridentate Schiff base ligands were prepared by the reactions of salicylaldehyde and 2-hydroxy-1-naphthaldehyde with 2-aminophenol and 2-amino-p-cresol. And then Cu(II) complexes of those ligands were synthesized. The structures and properties of ligands and their complexes were studied by elemental analysis, $^1H$-NMR, IR, UV-visible spectra, and thermogravimetric analysis. The mole ratio of Schiff base to the metal of complexes was found to be 1:1. Cu(II) complexes were contemplated to be four-coordinated square planar configuration containing one water molecule. The redox process of ligands and complexes in DMSO solution containing 0.1 M TBAP as a supporting electrolyte was investigated by cyclic voltammetry and differential pulse voltammetry with glassy carbon electrode. The redox process of the tridentate Schiff base ligands was totally irreversible. The redox process of Cu(II) complexes was quasi-reversible and diffusion-controlled as one electron by one step process Cu(II)/Cu(I). The reduction potentials of the Cu(II) complexes shifted in the positive direction in the order of [Cu(II)(HNIPC)($H_2O$)]>[Cu(II)(HNIP)($H_2O$)]>[Cu(II)(SIP)($H_2O$)]>[Cu(II)(SIPC)($H_2O$)].

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Stabilization of LiMn2O4 Electrode for Lithium Secondary Battery(I) - Electrode Characteristics on the Substitution of Metal Oxides in LiMn2O4 Cathode Material - (리튬이차전지용 정극활물질 LiMn2O4의 안정화(I) - LiMn2O4에 대한 금속산화물의 치환에 따른 전극 특성 -)

  • Lee, Jin-Sik;Lee, Chul-Tae
    • Applied Chemistry for Engineering
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    • v.9 no.5
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    • pp.774-780
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    • 1998
  • For the stabilization of the spinel structured $LiMn_2O_4$, a fraction of manganese was substituted with various metals such as Mg, Fe, V, W, Cr, Mo with Mn that had a similar ionic radii ($LiM_xMn_{2-x}O_4(0.05{\leq}x{\leq}0.02)$). The $LiM_xMn_{2-x}O_4$ showed a substantial improvement as lower capacity loss than that of the spinel structured $LiMn_2O_4$ when it was used as a cathode material. And with the partial substitution, the chemical diffusion coefficient for $LiMg_{0.05}Mn_{1.9}O_4$ and $LiCr_{0.1}Mn_{1.9}O_4$ was increased by and order of magnitude compared to that of the $LiMn_2O_4$ with spinel structure. The results showed that significant improvement can be made on the electrochemical characteristics as the structure of the $LiMn_2O_4$ electrode material was stabilized by the partial substitution.

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A Case Study on Performance Analysis of Antimicrobial Copper Film Attaching to Window for Responding to COVID-19 and Others (코로나19 등 대응을 위한 "유리창 부착용 항바이러스 동필름" 성능분석 사례연구)

  • Kim, Seong Je
    • Journal of Korean Society of Disaster and Security
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    • v.14 no.1
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    • pp.23-40
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    • 2021
  • In the era of the global coronal 19 pandemic, there is a risk of cross-infection in hospitals at the stage where treatments and vaccines are currently being developed and marketed, so individuals should enhance their acquired immunity and generalize their living systems by the performance of copper ions in the social environment. In order to prevent the spread of infection, the need for anti-bacterial film and its efficacy were analyzed through anti-viral performance tests based on research and development cases of worldwide and immemorial time. he Korea Construction Research Institute (KCL) has received anti-bacterial performance certification and anti-viral test scores from the "National Approval Performance Certification Agency." At the time, NCCP 43326 Human Corona virus (BetaCoV/Korea/KCDC03/2020), which was approved by the Centers for Disease Control and Prevention, was introduced to ensure that the activity rate of infected cells was satisfied in the anti-viral performance test. Anti-proliferation measures for the Corona 19 virus require a quality clinical trial study comparing the experimental group within the glass space where the antiviral copper film is constructed with the comparator of the same condition without copper film.

The color enhancement of natural ruby produced from Mong Hsu (Mong Hsu산 천연루비의 색상 개선)

  • Park Chun-Won;Kim Pan-Chae
    • Journal of the Korean Crystal Growth and Crystal Technology
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    • v.14 no.6
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    • pp.290-297
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    • 2004
  • The color enhancement of natural ruby produced from Mong Hsu were carried out by the heat treatment using gas diffusion. The natural ruby in this paper has a colored patch of which the color ranges from blue to a color close to black. The most favorable heat treatment conditions were as follows; range of temperature $1400~1600^{\circ}C$, duration 12 hrs, $O_2$ atmosphere. The color tone of ruby obtained under the optimum conditions was overall clear red by partial removal of colored patch. From EPMA results, part of blue or black colored patch within ruby were found to occur by charge transfer between $Fe^{2+}{\;}and{\;}Ti^{4+}$ . These results are consistent with the XRF that contents of $Fe(Fe^{2+}{\;}or{\;}Fe^{3+}$) and $Ti^{4+}$ ion to cause a blue or black colored patch after heat treatment became slightly less than with non-treated ruby. The silk formed on the surface of ruby heat treated for 12 hrs at $1700^{\circ}C$ were found to be generated by re-crystallization of rutile $TiO_2$ by XPS analysis.

Poly(vinyl alcohol) Membranes Containing Sulfonic Acid Groups for Direct Methanol Fuel Cell Application (설폰산기를 함유한 PVA막의 직접 메탄올 연료전지 응용)

  • Lee Young Moo;Lee Sun Yong
    • Membrane Journal
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    • v.14 no.3
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    • pp.240-249
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    • 2004
  • Crosslinked PVA membranes were achieved by esterification between the hydroxyl groups of PVA and carboxyl group of sulfosuccinic acid (SSA). SSA containing sulfonic group was used as a chemical crosslinking agent as well as a donor of fixed anionic group ($-SO_3$H). The crosslinking density of membranes was controlled by SSA content and calculated using polar and non-polar solvent. The crosslinking density measured by using non-polar solvent such as xylene and benzene increases with SSA content. However, using the polar solvent such as water and methanol, the crosslinking density increases up to SSA content of 20 wt% and above the content decrease due to sulfonic acid groups. The crosslinked PVA membranes were studied in relation with water diffusion coefficient and mechanical property as well as proton conductivity and methanol permeability as a function of crosslinking density. These properties were all dependent on the effect of SSA content.

Blocking Layer Coating on FTO Glass by Sol-Gel Method for Dye-Sensitized Solar Cell (염료 감응형 태양전지 효율 향상을 위한 졸-겔법을 이용한 차단막 코팅 방법)

  • Bae, Sang-Hoon;Han, Chi-Hwan;Kim, Do-Jin
    • 한국신재생에너지학회:학술대회논문집
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    • 2010.06a
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    • pp.96.1-96.1
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    • 2010
  • 현재 태양광 시장에 진출한 대부분의 Si계열 태양전지는 복잡한 공정과 원재료 고갈, 높은 가격으로 인해 한계에 직면에 있는 상태이다. 최근 많은 연구소나 학교에서는 기존의 Si계열 태양전지를 대체할 대안으로 염료 감응형 태양전지에 대해서 높은 관심을 보이고 있으며, 그동안의 연구개발로 단위 셀 면적에서는 상용화에 근접한 효율을 확보한 상태이다. 염료 감응형 태양전지의 작동과정을 간단히 단계별로 살펴보면 나노 결정 산화물 반도체 표면에 흡착된 염료분자가 가시광선을 흡수하면 전자는 HOMO에서 LUMO로 천이하고 이 들뜬 상태의 전자는 다시 에너지 준위가 낮은 반도체 산화물의 전도띠로 주입된다. 주입된 전자는 나노 입자간 계면을 통하여 투명 전도성막으로 확산, 전달되고 산화된 염료분자는 전해질 I-에 의해 다시 환원되어 중성 분자가 된다. 그러나 표면상태 전자 중 일부는 산화된 염료와 다시 결합하거나, 전해질의 $I^{3-}$ 이온을 환원시키기도 한다. 이와 같은 과정은 암전류를 증가시키면서 반도체 전극 막의 성능을 저해하는 주원인이 된다. 전자의 재결합은 투명 전극을 통해서도 가능하기 때문에 투명 전극에 얇은 blocking layer를 도포한 후 나노 결정 산화물 반도체 전극을 제작하면 전지 특성을 향상시킬 수 있다. 본 실험에서 우리는 졸-젤 법으로 $TiO_2$ blocking layer 졸을 만들었고 간단하며 저가공정이 가능한 스크린 프린팅 방법으로 blocking layer를 형성하는 실험을 진행하였다. 전도띠 에너지가 높은 반도체 물질로 표면을 처리하면 $TiO_2$-전해질 간 계면에 에너지 장벽이 형성되어 재결합을 줄여 모든 광전특성이 향상 되었다.

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