• Resources Recycling
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• v.10 no.3
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• pp.29-36
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• 2001

Cyclic voltammetry has been applied in the basic studies for the treatment and recovery of heavy metal component contained in wastewater by electrochemical reduction. The electrochemical behaviors of zinc ion for zinc metal electrode and carbon elec-trode were characterized by voltammograms and it was showed that zinc ions were reduced to metallic form below -0.76 V vs SHE. The change in the features of crystalline form of metallic zinc upon oxidation and reduction reaction was observed by X-ray diffraction method and the Am analysis verified that zinc ions were reduced to metal on copper plate. The results of this study were regarded to be important and meaningful in the treatment of heavy metal containing wastewater and, as a result, in the obtainment of metallic product by electrochemical method.

• Journal of Energy Engineering
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• v.24 no.3
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• pp.89-95
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• 2015

Carbon felts manufactured by (Co)CNF were subjected to heat treatment under different temperatures to use for the electrode of a redox-flow battery. BET and weight loss were tested to investigate the physical properties of the carbon felt according to the heat treatment conditions. SEM and XPS were also analyzed to characterize their surface area. In addition, electrical resistance, CV (cyclic voltammetry) and RFB charge on the electrode properties were examined in accordance with the heat treatment conditions with the discharge performance. The changes of physical properties on the carbon felt surface was confirmed via SEM and BET analysis, The most addition of oxygen functional groups on the carbon felt surface was obtained when one hour heat treatment at $550^{\circ}C$ and it was confirmed by XPS analysis. After resulting the CV tests, the active area of the electrode was the largest at $550^{\circ}C$ heat treatment. The heat treatment experiment of vanadium redox flow battery using the carbon felts were tested at $400^{\circ}C$, $500^{\circ}C$ and $550^{\circ}C$. As a result, the charge-discharge energy efficiency of the heat treatment electrode was 72.9% and 79.8%, at $400^{\circ}C$ and $500^{\circ}C$, respectively. The efficiency of the heat treatment electrode at $550^{\circ}C$ was the best as 79.8% at $550^{\circ}C$.

• Proceedings of the Korean Fiber Society Conference
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• 1998.10a
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• pp.512-516
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• 1998

탄소재료는 높은 전기전도도 및 기계적 강도, 화학적 안정성, 큰 비표면적(1000~3000$m^2$/g) 등의 특성 때문에 연료전지, 리튬이온 이차전지, 전기 이중층 캐패시터(electric double layer capacitor, EDLC).의 전극 활물질로 주목받고 있다[1]. 탄소섬유는 보통 특성과 전구체 핏치에 따라서 두 가지 종류로 분류된다[2]. 하나는 메조페이스 핏치로부터 제조된 고성능 탄소섬유(HPCF)이다. (중략)

• Applied Chemistry for Engineering
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• v.22 no.1
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• pp.114-118
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• 2011

Even though the carbon paste electrode bound with mineral oil is useful for research about the characteristics of enzymes, it remains far from practical uses because the lack of mechanical hardness limits its practical use. When the rubber liquefied in toluene was used as a binder of carbon powder in lab, it is confirmed that the mechanical robustness of the electrode is guaranteed. In order to confirm whether it shows quantitative electrochemical behaviors or not, its kinetic parameters, e.g. the symmetry factor (${\alpha}=0.28$), the exchange current density ($i_0=4.06{\mu}A/cm^2$), the capacity of the double layer ($C_d=2.11{\times}10^{-3}F$), the Michaelis constant ($K_M=2.45{\times}10^{-3}M$), and the time constant (${\tau}_B=0.077sec$) were investigated. Our experimental observations prove that the chloroprene rubber is a promising binder for the practical use of a carbon paste electrode.

• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 2004.07b
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• pp.1199-1202
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• 2004

리튬이온전지 음극활질용으로 Hybrid of pitch based graphite impregnating natural graphite와 Hybrid of pitch based carbon impregnating natural graphite로 탄소전극을 제작하여 전기화학적인 특성을 연구하였다. Natural graphite에 pitch based graphite나 pitch based carbon의 혼합은 흑연의 이론용량인 372 mAh/g를 초과하는 고용량을 나타내었다. 이것은 극소공동에 리튬종의 삽입과 탈삽입에 의한 것으로 파악된다. 그러나 충 방전이 계속 진행되면서 방전용량이 급격히 저하되는 현상이 관찰되었다. X-선 회절분석 결과로부터 Hybrid of pitch based carbon impregnating natural graphite 탄소전극에는 amorphous carbon이 상대적으로 다량 존재한다는 것을 확인하였고, 이는 리튬의 삽입된 상태의 전위에 분포가 있어 충 방전시에 완만한 전압의 구배를 만들며, 비가역용량을 증가시키는 요인으로 파악되었다.

• Applied Chemistry for Engineering
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• v.24 no.3
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• pp.247-252
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• 2013

Sulfonated poly(ether ether ketone) (SPEEK) with a certain degree of sulfonation were synthesized by reacting PEEK and sulfuric acid at different reaction time. Then ion-selective composite carbon electrodes (ISCCE) were fabricated by coating the prepared SPEEK on the surface of carbon electrodes. The specific capacitance and resistance of the ISCCE were analyzed by electrical impedance spectroscopy. The ion exchange capacities (IEC) of the SPEEKs were measured in the range of 1.60~2.57 meq/g depending on the sulfonation time. The SPEEK more than 2.5 meq/g of IEC was considered unsuitable for fabricating the ISCCE because it was dissolved in water. The specific capacitance of the prepared ISCCE increased with increasing the IEC of coated SPEEKs and the capacitance was improved up to about 20% compared to that of uncoated carbon electrode. In addition, the electrical resistance of coating layer decreased significantly with increasing the IEC of coated SPEEKs. It is expected that the desalination efficiency of conventional capacitive deionization process can be improved by using the prepared ISCCE coated with SPEEK.

• Membrane Journal
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• v.28 no.4
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• pp.271-278
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• 2018

In this study, the carbon electrodes using activated carbon fibers (ACFs) were prepared for the capacitive deionization process. The Polyvinylidene fluoride (PVDF) was used as the binder and the mixed ACFs with proper solvent was cast on the commercial graphite sheets to prepare the carbon electrodes. At this moment, the different particle sizes of ACFs were applied and the mixing ratio of solvent, PVDF and ACFs, 80 : 2 : 18 and 80 : 5 : 15, were used for the electrode preparation. Then their salt removal efficiencies were characterized under the various operating conditions, adsorption potential and time, desorption potential and time, concentration of feed NaCl solution and flow rate as well. Typically, the salt removal efficiency of 53.6% were obtained at the particle size below $32{\mu}m$, mixing ratio 80 : 2 : 18, adsorption 1.2 V and 3 min, desorption -0.1V and 1 min, and 15 mL/min flow rate of NaCl 100 mg/L.

• Composites Research
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• v.33 no.6
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• pp.336-340
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• 2020

In this study, carbon aerogels (CA) were prepared by sol-gel polycondensation of resorcinol and furfural in isopropanol using hexamethylenetetramine as a catalyst, and then directly drying the organic gels under isopropanol freeze-drying conditions, followed by carbonization under a nitrogen atmosphere. The preparation conditions of the CA were explored by changing the mole ratio of resorcinol to furfural. The effect of the preparation conditions on the pore structure of the CA was studied by nitrogen adsorption isotherms. The characteristics of the CA were studied by scanning and transition electron microscopy, and infrared spectrometry. The accessibility of pores and performance of the CA as an electrode in electric double layer capacitors were also electrochemically investigated. As a result, BET surface area and specific capacitance increased with the molar ratio of resorcinol to catalyst (R/C) ratio; the maximum values of 765 ㎡/g and 132 F/g were achieved at the R/C ratio of 200, respectively. Consequently, it was confirmed that increasing the R/C ratio increased the average pore size of the CA electrode, which improved the rate capability of the system.

• Journal of the Korean Electrochemical Society
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• v.12 no.3
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• pp.263-270
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• 2009

Carbon felt surface was modified by heat or acid treatment in order to use for the electrode of a redox-flow battery. Polymers on the surface of carbon felt was removed and oxygen-containing functional group was attached after the thermal treatment of carbon felt. Thermal treatment was better for the stability of the carbon structure than the acid treatment. Oxygen-containing functional group on the thermally treated carbon felt at 500$^{\circ}C$ was confirmed by XPS and elementary analysis. BET surface area was increased from nearly zero to 96 $m^2/g$. Thermally treated carbon felt at 500$^{\circ}C$ showed lower activation polarization than the thermally treated carbon felt at 400$^{\circ}C$ and the acid-treated carbon felt in the cyclicvoltammetry and polarization experiments. The thermally treated carbon felts at 400$^{\circ}C$ and 500$^{\circ}C$ and the acid-treated carbon felt was applied for the electrode to prepare vanadium redox flow battery. Voltage efficiencies of charge/discharge were 86.6%, 89.6%, and 96.9% for the thermally treated carbon felts at 400$^{\circ}C$ and 500$^{\circ}C$ and the acid-treated carbon felt, respectively.

• Composites Research
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• v.35 no.6
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• pp.394-401
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• 2022

Two polymer precursors, polyvinylidene chloride-resin (PVDC-resin) and polyvinylidene fluoride (PVDF), are assembled into the microporous carbon by pyrolysis. Microporous carbon is advantageous as an electrode for supercapacitors that store electric charges through ion adsorption/desorption. The pyrolysis also turns the various heteroatoms of two precursors into functional groups, contributing to the additional charge storage. The analysis of the porous structure and function group during carbonization are important to develop the carbon for energy storage. Here, we analyzed the functional groups of two polymer-derived carbons through X-ray photoelectron spectroscopy. The electrochemical properties of the functional groups were explored in various pH electrolytes. The specific capacitance of two carbons in the acidic electrolyte (1 M H₂SO₄) was improved compared to that in the neutral electrolyte (0.5 M Na₂SO₄) due to the faradaic charge/discharge reaction of the quinone functional group. In particular, the carbon electrode derived from PVDC-resin exhibits a lower capacity than the carbon from PVDF due to the small micropores. In the alkaline electrolyte (6 M KOH), the highest specific capacitance and rate capability were obtained among the three electrolytes for both electrodes based on the facile adsorption of the constituent electrolyte ions (K⁺, OH^-).