• 한국응용과학기술학회지
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• 제28권1호
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• pp.48-56
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• 2011

In this study, we investigated the C-V diagrams and metal surface related to the electrochemistry characterization of metal(nickel, SUS-304). We determined electrochemical measurement by using cyclic voltammetry with a three-electrode system. A measuring range was reduced from initial potential to -1350mV, continuously oxidized to 1650 mV and measured to the initial point. The scan rate were 50, 100, 150, 200 and 250 mV/s. As a result, the C-V characterization of metal using N,N-dimethylacetamide and N,N-dimethylformamide inhibitors appeared irreversible process caused by the oxidation current from the cyclic voltammogram. After adding organic corrosion inhibitors, adsorption film constituted, and the passive phenomena happened. According to the results by cyclic voltammetry method, it was revealed that the addition of inhibitors containing amide functional group enhances the corrosion resistance properties.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2006년도 총회 및 춘계학술발표회
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• pp.16-19
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• 2006

Humin is the insoluble fraction of humic materials and play an important roles in the irreversible sorption of hydrophobic organic contaminants onto soil particles. However, there have been limited knowledge about the sorption and chemical properties of humin due to the difficulties in its separation from the inorganic matrix(mainly clays and oxides). In this study, do-ashed humin was isolated from a soil sample after removing free lipid and alkali-soluble humic fractions followed by dissolution of mineral matrix with 2% HF, and characterized by elemental analysis, C-13 NMR spectroscopic method. Sorption behavior of 1-naphthol with humin was also investigated from aqueous solution. C-13 NMR spectra indicate that humin molecules are mainly made up of aliphatic carbon including carbohydrate, methylene chain etc.. Sorption intensity for 1-naphthol was increased as organic carbon content of humin increased and log Koc values for the 1-naphthol sorption were determined to be ${\sim}3.12$

• Bulletin of the Korean Chemical Society
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• 제12권5호
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• pp.487-490
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• 1991

Electrochemical studies of alkali metal cations $(Na^+, K^+, Rb^+, Cs^+)$ were performed in methanolic solutions of 18-crown-6 and tetrabutylammonium salts at dropping mercury electrodes (DME) and thin mercury film electrodes (TMFE). All the cations investigated were reduced reversibly at DME in the absence and presence of 18-crown-6, and in the latter the limiting currents were decreased and the reduction potentials shifted to the negative direction. The reduction potentials of the metal ions (0.2 mM) in the presence of the crown (10 mM) were - 2.14 $(Na^+)$, - 2.26 $(K^+)$, - 2.20 $(Rb^+) and - 2.14 $(Cs^+)$ V vs. SCE, respectively. The measured potentials were rationalized with ion recognition of the cations by the crown. Electroreduction at TMFE were highly irreversible. A new representation method of ion recognition is presented. In aqueous solutions, electroreduction of the alkali metal ions were characterized by adsorption.

• 대한지하수환경학회지
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• 제6권2호
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• pp.95-100
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• 1999

토립자 표면에서의 흡착에 의한 토양에서의 탄화수소계 화합물의 지연효과는 잘 알려진 현상이다. 본 연구에서는 배치시험과 주상시험을 수행함으로써 사질토양에서 Benzene의 이동성에 대한 지연효과를 조사하였다. 배치시험을 위하여 토양시료와 다양한 초기농도의 Benzene 용액을 48시간 반응시켰고. 초기용액과 평행상태의 Benzene 용액의 농도를 HPLC를 이용하여 분석하였다. 주상시험은 파괴곡선으로 알려진 시간에 따른 용액의 농도를 측정함으로써 수행되었다. 추적자로는 10 g/L 농도의 KCI과 0.88 g/L의 Benzene 용액을 사용하였고 .각각의 용액을 토양시료의 상부경계면에 순간주입한 후 정상류 상태에서 배출구로 빠져나온 용탈수의 농도를 EC-meter와 HPLC를 이용하여 측정하였다. 배치시험의 결과로부터 linear adsorption isotherm에 의한 분배계수가 측정되었고 주상시험 조건의 용적밀도 및 함수율을 고려한 지연계수가 산정되었다. 주상시험의 결과 i) Benzene의 첨두농도는 KCl 첨두농도보다 상당히 낮았으나. ⅱ) 첨도농도의 도달시간은 거의 일치하였다. 첨두농도의 도달시간이 일치한다는 결과는 지연효과가 일어나지 않았다는 것을 지시하며, 배치시험의 결과로부터 산정된 지연계수를 고려하여 예측된 파과곡선은 Benzene의 주상시험 결과와 일치하지 않았다. Benzene 농도의 뚜렷한 감소를 설명할 수 있는 유일한 방법은 convection-dispersion equation(CDE) 모델에서 비가역 흡착에 의한 농도의 절대적 감소를 고려하는 감쇄계수(decay or sink coefficient)를 적용해야 하는 것으로 판단된다.

• 공업화학
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• 제8권2호
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• pp.267-275
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• 1997

본 연구는 졸-겔법을 이용하여 제조한 $ZrO_2$의 하소 온도에 따른 분말특성을 조사하고, 고온수에서 $ZrO_2$의 $Co^{2+}$ 흡착특성을 교반기가 달린 압력용기를 이용한 회분식 흡착 실험으로 알아보았다. 졸-겔법을 이용하여 $ZrO_2$분말을 제조하고, $600{\sim}1400^{\circ}C$로 하소한 후, X-선 회절법, SEM, BET 방법, Fourier transform 적외선 (FT-IR), 열중량 및 열시차분석법(TG-DTA)등을 이용하여 특성 변화를 조사하였다. 비정질의 질코니아는 $480^{\circ}C$부터 tetragonal 질코니아가 생성되고 $600{\sim}1000^{\circ}C$ 온도범위에서는 tetragonal 질코니아와 monoclinic 질코니아가 공존하며, $1200^{\circ}C$에서는 tetragonal 질코니아에서 monoclinic 질코니아로의 상변태가 나타났으며, 고온수에서 하소온도가 $600^{\circ}C$인 $ZrO_2$의 흡착제의 코발트 평형흡착용량은 0.16 meq/g 이었다. $125^{\circ}C$ 이상의 고온에서의 흡착반응은 비가역 흡열반응이며, $600^{\circ}C$에서 하소한 $ZrO_2$의 표준엔탈피 변화값(${\Delta}H^{\circ}$)은 약 18 kJ/gmol 이였다.

• 공업화학
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• 제7권6호
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• pp.1192-1203
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• 1996

알루미늄 및 티타늄 알콕사이드의 가수분해방법을 인용하여 고온수중에 적용할 수 있는 $Al_2O_3-TiO_2$ 복합옥사이드형 흡착제를 제조하였다. 제조한 흡착제는 $600{\sim}1400^{\circ}C$의 온도로 하소되었으며, 결정전이, 열적 특성, 비표면적 등의 물성변화를 알아 보기 위하여 X선회절, 적외선분광분석, 열분석 전자현미경 관찰, BET 방법에 의한 측정 등을 수행하였다. 그리고 Autoclave를 이용한 회분식 흡착실험으로 이 흡착제들의 $TiO_2$ 함량 및 하소 온도 변화에 따르는 고온수중에서의 $Co^{2+}$ 흡착 특성을 알아 보았다. $150{\sim}250^{\circ}C$의 온도 범위에서 $Al_2O_3-TiO_2$ 흡착제의 $Co^{2+}$ 흡착반응에 대한 표준 엔탈피 변화값은 $TiO_2$ 함량이 26mol%, 43mol%, 80mol%에 대하여 $16.5{\sim}26.0kJ{\cdot}mol^{-1}$범위에 있었으며, 이 흡착반응이 비가역적인 흡열반응임을 알 수 있었다. $250^{\circ}C$의 고온수에서 하소 온도가 $600^{\circ}C$, $TiO_2$함량이 26mol%인 흡착제의 코발트 평형흡착용량은 $0.1674meq{\cdot}g^{-1}$이었다.

• Journal of Electrochemical Science and Technology
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• 제12권3호
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• pp.323-329
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• 2021

This work presents a contrasting behavior of formic acid oxidation (FAO) on the Pt and Bi deposits on different Pt substrates. Using irreversible adsorption method, Bi and Pt were sequentially deposited on Pt electrodes of nanoparticle (Pt NP) and disk (Pt disk). The deposited layers of Bi and Pt on the Pt substrates were characterized with X-ray photoelectron spectroscopy, transmission microscopy and scanning tunneling microscopy. The electrochemical behaviors and FAO enhancements of Pt NP and Pt disk with deposited Bi only (i.e., Bi/Pt NP and Bi/Pt disk), were similar to each other. However, additional deposition of Pt on Bi/Pt NP and Bi/Pt disk (i.e., Pt/Bi/Pt NP and Pt/Bi/Pt disk) changed the electrochemical behavior and FAO activity in different ways depending on the shapes of the Pt substrates. With Pt/Bi/Pt NP, the hydrogen adsorption was suppressed and the surface oxidation of Pt was enhanced; while with Pt/Bi/Pt disk, the opposite behavior was observed. This difference was interpreted as a stronger interaction between the deposited Bi and Pt on Pt NP than that on Pt disk. The FAO performance on Pt/Bi/Pt NP is much better than that on Pt/Bi/Pt disk, most likely due to the difference in the interaction between the deposited Pt and Bi depending on the shapes of Pt substrates. In designing FAO electrochemical catalysts using Pt and Bi, the shape of a Pt substrate was concluded to be critically considered.

• 상하수도학회지
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• 제23권6호
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• pp.855-864
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• 2009

The main object of this work was to determine the influence of periodic chemical backwash on filtration resistance in membrane filtration system. In this work Hermia's models were used to investigate the fouling mechanisms involved in the microfiltration of $0.45{\mu}m$ filtered sewage feed. Batch microfiltration experiments were performed at transmembrane pressure 0.4 bar and different feed SCOD concentration (9~67 mgSCOD/L). The results showed that the best fit to experimental data corresponded to the intermediate blocking model followed by the standard and complete blocking model for all the experimental conditions tested. From the simulation results of filtration performance, it was found that in order to maintain sustainable operation of membrane filtration system, irreversible foulant component accumulated continuously on membrane surface and/or pore must be effectively removed. In addition, it was verified that periodic chemical backwash using NaOCl or NaOH effectively improved filtration performance of membrane.

• Bulletin of the Korean Chemical Society
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• 제18권4호
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• pp.385-389
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• 1997

We report on the development of a new method to control the coverage of a metal film prepared with immersion method. An Sb species in solution adsorbed irreversibly at an open circuit potential (∼0.2 V) as an oxygenous Sb(Ⅲ) on a clean Au electrode, and the adsorbates showed voltammetric features in the potential range from 0.1 V to - 0.4 V. The full coverage of the Sb adsorbates was ∼0.45. On the contrary, the Sb species in solution did not adsorb at all on iodine-covered Au electrode surfaces, when the iodine coverages were more than 0.25. As the iodine coverage decreased below 0.25, however, the irreversible adsorption of Sb took place and the coverage of Sb increased accordingly. This electrochemical behavior has been interpreted as the penetration of the adsorbing Sb species in solution through open spaces among the iodine adlattices of coverages less than 0.25. With the manipulation of the iodine coverage, the controllable range of Sb coverage was from 0 to 0.45, i.e. the full coverage of Sb. In addition, the reversible deposition of Sb on an iodine-saturated Au electrode with voltammetric scan has been observed, which is contrasted with the adsorptive behavior of Sb on the clean Au electrode.

• Bulletin of the Korean Chemical Society
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• 제8권4호
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• pp.225-230
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• 1987

The redox properties of 2-mercaptopyridine N-oxide (mpno) and its oxovanadium complex, $VO (mpno)_2$ have been studied by the use of polarography and cyclic voltammetry. The radical anion of mpno is generated in acetone and is adsorbed to the electrode to form an adsorption wave at -0.21 V vs Ag/AgCl electrode. The normal wave appeared at -0.50 V is attributed to the formation of radical anion. The $VO (mpno)_2$ exhibits one oxidation wave at +0.57 V, and two reduction waves at -1.07 V and -1.76 V vs. Ag/AgCl electrode; the oxidation is fully reversible one-electron process ($VO (mpno)_2\;{\leftrightarrow}\;VO(mpno)_2^+ + e).$ The reduction wave at -1.07 V is quasireversible and is arised from the formation of $VO (mpno)_2^-.$ The second reduction wave at -1.76 V is irreversible and this reduction process consists of two one-electron steps. The sulfur containing ligands seem to enhance the stability of lower oxidation state of vanadium while the oxygen or nitrogen donor of the ligands stabilize the higher oxidation state of vanadium when comparisons are made among several oxovanadium complexes.