• 폴리머
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• 제24권4호
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• pp.499-504
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• 2000

고강도 PAN계 탄소섬유를 양극산화하여 섬유의 표면 관능기와 표면 자유에너지, 그리고 최종 복합재료의 기계적 특성 향상에 미치는 영향을 고찰하였다. FT-IR과 XPS 측정 결과, 양극산화에 의해 형성된 섬유 표면의 산소 관능기는 섬유의 표면 에너지와 복합재료의 층간 전단강도 (ILSS)에 큰 영향을 주는 것으로 나타났다. 그리고 젖음액의 wicking rate에 근거한 접촉각 측정에서 탄소섬유의 양극산화는 표면 자유에너지의 극성 요소를 크게 증가시키며, 이것은 표면 에너지 관점에서 살펴볼 때 좋은 젖음성이 최종 복합재료의 섬유와 에폭시 수지 매트릭스사이의 계면결합력 향상에 중요한 역할을 하는 것으로 나타났다. 또한 본 연구에서는 섬유 표면의 $O_{1s}$ $C_{11}$ ratio 또는 극성 요소와 복합재료의 ILSS사이에서 직선적인 상관관계를 나타낼 수 있었다.다.

• 폴리머
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• 제25권6호
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• pp.866-875
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• 2001

본 연구에서는 고온 산화분위기 하에서 탄소/탄소 복합재료의 열적 향상을 위해 사용된 tetraethylorthosilicate(TEOS)의 첨가량에 따른 복합재료의 kinetic parameter에 기초한 열분해 메카니즘 및 열안정성을 열중량분석기(TGA)를 사용하여 고찰하였다 TEOS를 함유한 탄소/탄소 복합재료의 kinetic parameter, 즉 열분해 활성화 에너지 ($E_d$), 반응차수(n), 지수앞 인자 (A)는 각각 136 kJ/mol, 0차, 및 2.3$\times$$10^9s^{-1}$을 나타내었으며, 특히 IPDT 및 $E_d$로부터 살펴본 복합재료의 열안정성은 탄소/탄소 복합재료에 TEOS가 첨가되면 크게 향상되었는데, 이는 산소에 대한 산화방지막, 즉 $SiO_2$의 형성으로 인한 복합재료 표면에서의 카본 활성종에 산소의 침투를 방해하여 TEOS를 함유한 복합재료가 이를 함유하지 않은 것에 비하여 표면 산화 속도가 감소되어 열안정성이 증가하였다고 사료된다.

• 한국세라믹학회지
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• 제23권1호
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• pp.51-59
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• 1986

It was the first time the MgO-C brick was developed for the lining materials in the hot spots in electric are furnace in 1972. MgO-C brick is high registant to thermal and structural spalling. Futhermore for the reason that carbon is hard to react with slag and MgO is high fireproof MgO-C brick shows a high corrosion registance to slag attack compared with conventional basic refractories. Owing to their excellent properties the use of MgO-C refractories are being developed widely in the field of shaped refractories and even in that of monolithic refractories. In this paper the oxidation of carbon the infiltration of slag into the brick texture and effects of additions were investigated. The results obtained were as follows : 1) The use of fused MgO-clinker and high purity carbon as raw materials increased the corosion registance and hot modulus of rupture of MgO-C brick. 2) As the oxidation reaction of the carbon proceeded the slag infiltrated into the brick texture. And then the slag components reacted with the MgO grains and formed low melting point compounds particulary CaO.MgO.$SiO_2$ and 3CaO.MgO.$2SiO_2$ that resulted in the wear of the brick. 3) It is recongnized the Al, Si, $B_3C$ effects on the oxidation registant properties of MgO-C brick by contribu-ting to the decrease of permeability according to the formation of $Al_4C_3$, SiC, $B_2O_3$ and the decrease of open pores relating to the formation of MgO.Al2O3, $SiO_2$, 3MgO.$B_2O_3$ at the decarbonized layer.

• 한국환경과학회지
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• 제8권4호
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• pp.539-545
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• 1999

Dye wastewater was treated by using an electrochemical oxidation process. Various combinations of electrodes such as carbon, Al and Fe were investigated. In this study, electrode material, electrolyte concentration, electrode distance, current density, and pH value were found to have significant effect on both pollutant removal efficiency and current efficiency in electrochemical oxidation process. After electrolysis for 40min with carbon/Al, it was observed that COD, $T-N, NH_{4}^{+}-N$ and color of treated wastwater were reduced from 580mg/$\ell$ to 145mg/$\ell$, 67.2mg/$\ell$ to 26.8mg/$\ell$, 46.8mg/$\ell$ to 1.4mg/$\ell$, and 4200 Pt-Co units to 336 Pt-Co units, respectively. The optimal conditions of the electrooxidation process to treat the wastewater for this study were found to be such : current density ; 16.67mA/$cm^2$, electrode distance ; 2.5cm, pH value ; 5.0 and carbon/Al electrode.

• 해양환경안전학회:학술대회논문집
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• 해양환경안전학회 2003년도 춘계학술발표회
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• pp.205-209
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• 2003

The various pretreatment processes were evaluated for removal of oil pollutants with weathered oil contaminated seawater in a reverse osmosis desalination process. Weathered oil contaminated seawater was made by biodegradation and photooxidation with oil containing seawater. Coagulation, ultrafiltration, advanced oxidation processes and granular activated carbon filtration was used with pretreatment for dissolved organic carbon. Crude oil was removed but. weathered oil contaminated seawater was not removed by biodegradation and coagulation. DOC and E260 was removed with about 20 % and 40 % by membrane filter of cut off molecular weight 500. So, the most of dissolved organic carbon in weathered oil contaminated seawater was revealed that molecular weight was lower than 500. It is difficult to remove DOC in weathered oil contaminated seawater by advanced oxidation processes treatment, but, E260 was removed more high. However, DOC in weathered oil contaminated seawater was easily adsorbed to GAC. It is revealed that DOC was removed by adsorption.

• 한국기계연구소 소보
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• 통권15호
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• pp.57-66
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• 1985

Fibers with a high degree of axial preferred orientation can be obtained from mesophase pitch. Prior to cabonization, the pitch fibers must be rendered in fusible so that their orientation is preserved. The stabilization of the pitch fibers was heated at temperature between $250^{circ}C$ and $300^{circ}C$ and a treatment time 5 to 80minutes. Oxidized fibers heated $1800^{circ}C$without stretching. Pitch based carbon fiber have a young's modulus as high as 304GN/$m^2$. The structure of the pitch cased carbon fiber is determining factor for the mechanical properties of the produced fibers. The structure depending on the pitch precursor as well as on the oxidation time.

• Journal of Electrochemical Science and Technology
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• 제5권1호
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• pp.23-31
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• 2014

The DL-norvaline was electrochemically oxidized and deposited on the glassy carbon electrode surface using cyclic voltammetry (CV). The modified electrode was examined for electrochemical oxidation of hydroquinone (HQ) and catechol (CC). It exhibited good electrocatalytic ability towards their oxidation and simultaneous determination in a binary mixture using differential pulse voltammetry (DPV). The peak currents were linear to the concentration of HQ and CC, in the range from $5{\mu}M$ to $100{\mu}M$, and $4{\mu}M$ to $140{\mu}M$, respectively. The determination limits(S/N = 3) for HQ and CC were $1{\mu}M$ and $0.8{\mu}M$, respectively. The obtained modified electrode was applied to simultaneous detection of HQ and CC in water sample.

• Bulletin of the Korean Chemical Society
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• 제26권10호
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• pp.1560-1564
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• 2005

The influence of cetyltrimethylammonium bromide (CTAB) on the electrochemical behavior of bisphenol A at the carbon paste electrode (CPE) was investigated. CTAB, with a hydrophobic C-H chain, can adsorb at the CPE surface via hydrophobic interaction and then change the electrode/solution interface, and finally affects the electrochemical response of bisphenol A, confirming from the remarkable oxidation peak current enhancement. The electrode process of bisphenol A was examined, and then all the experimental parameters which affects the electrochemical response of bisphenol A, such as pH value of the supporting electrolyte, accumulation potential and time, potential scan rate and the concentration of CTAB, were examined. Finally, a sensitive and simple voltammetric method was developed for the determination of bisphenol A. Under the optimum conditions, the oxidation peak current of bisphenol A varied linearly with its concentration over the range from $2.5\;{\times}\;10^{-8}\;to\;1\;{\times}\;10^{-6}$ mol/L, and the detection limit was found to be $7.5\;{\times}\;10^{-9}$ mol/L. This method was successfully employed to determine bisphenol A in some waste plastic samples.

• 한국세라믹학회지
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• 제41권9호
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• pp.657-662
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• 2004

마그카본계 내화물의 산화저항성을 증대시키기 위하여 섭씨 100$0^{\circ}C$에서 120$0^{\circ}C$에서 산화기구를 조사하고, TiC를 첨가하여 산화저항성 증가에 대한 효과를 관찰하였다. 산소공급을 위해 공기를 분당 0.2리터의 속도로 흘려주었으며 열천칭으로 무게변화가 없어질 때까지 매 30초 간격마다 무게감소를 측정하였다 본 실험에서 사용된 마그카본계 시편의 산화거동과 관련한 유효확산 계수는 1.39${\times}$$10^{-4}$ $m^2$/sec이다. 이러한 실험조건에서 총체적인 산화공정은 산화된 기공층을 통하여 내부로 향하는 산소의 확산에 의해 지배되는 반응으로 해석할 수 있다. TiC를 첨가한 시편은 마그카본계 내화물의 산화 저항성을 증대시켰다.

• 대한안전경영과학회지
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• 제2권4호
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• pp.187-195
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• 2000

Electrochemical promotion of the reaction rate was investigated for CO oxidation in a solid electrolyte catalytic reactor where a thin film of Pt was deposited on the yttria stabilized zirconia as an electrode as well as a catalyst. It was shown under open circuit condition that potential was a mixed potential of $O_2$exchange reaction and electrochemical reaction induced by CO. The effect of electrochemical modification on the CO oxidation rate was studied at various overpotentials and $P_{CO}$$P_{O2}$.