• 공업화학
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• 제23권1호
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• pp.47-52
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• 2012

다공성 탄소나노섬유의 아민 작용기에 따른 $CO_2$ 가스 감응특성을 고찰하고자, 아민작용기가 도입된 다공성 탄소나노섬유 기반 $CO_2$ 가스센서를 제조하였다. Polyacrylonitrile를 전구체로 하여 전기방사법을 통해 나노섬유를 제조하였으며, 열처리 및 화학적 활성화 공정, 그리고 Diethylenetriamine 액상처리법을 통하여 아민작용기가 도입된 다공성 탄소나노섬유를 제조하였다. BET 비표면적 분석결과, 화학적 활성화법에 의해 최대 $2000m^2/g$까지 탄소나노섬유의 비표면적이 향상됨을 확인하였으며, FT-IR 분광법을 통해 아민 작용기의 도입을 확인하였다. 아민 작용기가 도입된 가스센서의 $CO_2$ 가스 감응특성은 다공성 탄소섬유 기반 가스센서에 비해 약 4배 향상됨을 확인하였다. 결과적으로 화학적 활성화법에 의해 발달된 기공특성과 아민작용기 도입에 따른 화학흡착 유도에 의하여 감응특성이 향상되었음을 확인하였다.

• Carbon letters
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• 제12권1호
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• pp.31-38
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• 2011

This study experimentally investigated dicyclohexylammonium 2-cyanoacrylate (CA) as a potential comonomer for polyacrylonitrile (PAN) based carbon fiber precursors. The P(AN-CA) copolymers with different CA contents (0.19-0.78 mol% in the feed) were polymerized using solution polymerization with 2,2-azobis(isobutyronitrile) as an initiator. The chemical structure and composition of P(AN-CA) copolymers were determined by proton nuclear magnetic resonance and elemental analysis, and the copolymer composition was similar to the feeding ratio of the monomers. The effects of CA comonomer on the thermal properties of its copolymers were characterized differential scanning calorimetry (DSC) in nitrogen and air atmospheres. The DSC curves of P(AN-CA) under nitrogen atmosphere indicated that the initiation temperature for cyclization of nitrile groups was reduced to around $235^{\circ}C$. The heat release and the activation energy for cyclization reactions were decreased in comparison with those of PAN homopolymers. On the other hand, under air atmosphere, the P(AN-CA) with 0.78 mol% CA content showed that the initiation temperature of cyclization was significantly lowered to $160.1^{\circ}C$. The activation energy value showed 116 kJ/mol, that was smaller than that of the copolymers with 0.82 mol% of itaconic acids. The thermal stability of P(AN-CA), evidenced by thermogravimetric analyses in air atmosphere, was found higher than PAN homopolymer and similar to P(AN-IA) copolymers. Therefore, this study successfully demonstrated the great potential of P(AN-CA) copolymers as carbon fiber precursors, taking advantages of the temperature-lowering effects of CA comonomers and higher thermal stability of the CA copolymers for the stabilizing processes.

• 한국염색가공학회지
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• 제12권1호
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• pp.52-60
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• 2000

In the prior studies, we reported that the dye uptakes of C. I. Disperse Violet 1 on polyester fiber in hexane and cyclohexane were higher than those in the other solvents, as the number of carbon atoms of alkanes decreased, the dye uptake increased, and the logarithmic plot of the dye uptakes vs. the solubilities of the dye showed that the dye uptakes are inversely proportional to the solubilities. In this study, for Interpretation of dyeing behavior of C. I. Disperse Violet 1 on polyester in alkanes, the thremodynamic parameters of dyeing, such as standard affnity, heat of dyeing(enthalpy change), entropy change, diffusion coefficient, and activation energy of diffusion, were obtained from isotherms and dyeing rates at different temperature. As the number of carbon atoms of alkanes increased, the standard affinity decreased, but the heat of dyeing(enthalpy change) and the entropy change showed larger negative values. These results mean that as the number of carbon atoms of alkanes increases, the dye uptake decreases, but both the fraction of the dye molecules dyed at relatively highly aligned or compact region of polyester fiber and the regularity of dye aggregates in the fiber become increased. As the number of carbon atoms of alkanes increased, the diffusion coefficient decreased, but the activation energy of diffusion increased. In the alkane of larger number of carbon atoms, because the solubility of the dye is higher, the desorption rate of the dye is faster and the diffusion coefficient is smaller than those in the smaller alkanes. But the energy required to separate the dye molecules from the alkane molecules is much higher because the interaction between the alkane molecule and the dye molecule become strong with the number of carbon atoms.

• 대한화학회지
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• 제55권5호
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• pp.819-823
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• 2011

The relationship between the microstructure, mechanical properties, and oxidation behavior of pitch-, polyacrylonitrile (PAN)-, and Rayon-based carbon fibers (CFs) has been studied in detail. Three types of carbon fiber were exposed to isothermal oxidation in air and the weight change was measured by thermogravimetric analyzer (TGA) apparatus. After activation energy was gained according to the conversion at reacting temperature, the value of specific surface area and the surface morphology was compared, and the reaction mechanism of oxidation affecting development of pores of carbon fibers was examined. This study will lead to a new insight into the relationship between the microstructure and mechanical properties of carbon fibers.

• 약학회지
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• 제32권3호
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• pp.187-193
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• 1988

An activated carbon which showed big adsorption capacities of iodine, potassium permanganate and phenol was prepared from the Korean ricechaff. By scanning electron micrographs and IR spectra, it was observed that the organic components in the rice-chaff were decomposed to carbon dioxide and vapor by the pyrolysis and the activation, that activated carbon particles had carbon-carbon structures with a lot of microporosity. The adsorption capacities of iodine, potassium permanganate and phenol were determined. The adsorption isotherm of phenol was well fitted in Freundlich's equation.

• 한국연소학회지
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• 제8권2호
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• pp.27-33
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• 2003

Synthesis of carbon nanomaterials on a metal substrate by an ethylene fueled inverse diffusion flame was illustrated. Stainless steel plates were used for the catalytic metal substrate. The effects of catalyst metal particles were investigated through $Fe(NO_3){_3}$ (ferric nitrate, nonahydrate) and $Ni(NO_3){_2}$ (nickel nitrate, hexahydrate). Carbon nanotubes and nanofibers with diameters of $30{\sim}70nm$ were found on the substrate for the case of using SUS304 substrates only and using them with metal nitrates. In case of using metal nitrates, due to the easy activation of the metal particles, the formation and growth of carbon nanomaterials were occurred in the lower temperature region than that of using SUS304 substrates only.

• 공업화학
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• 제10권3호
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• pp.419-426
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• 1999

가황고무의 가황반응에 대하여 가황시스템 및 온도, 보강성충전제 첨가량 변화에 의한 반응속도상수 및 활성화에너지, 가교밀도 및 탄성상수, 가황특성 ($t_5,\;t_{90}$), 고무보강성 및 내마모성을 고찰하였다. 반응속도상수는 보강성충전제 첨가량, 가황시스템 및 가황반응온도에 대한 의존성이 크게 나타났으며, 반응온도에 따라 지수적으로 증가하였다. 활성화에너지는 가황시스템중 촉진제에 대한 황 비율이 높은 가황시스템에서 가장 작게 나타났으며, 보강성충전제 첨가량이 적을수록 작게 나타났다. 카본블랙 첨가량 변화는 고무보강성 및 내마모성에 직접적으로 영향을 미치고 있으나, 가황시스템 변화는 각기 다른 영향이 나타났다. 카본블랙 첨가량이 증가하면 모듈러스가 증가하고, 내마모성이 향상되며, 스코치시간이 짧아졌으나, 가교밀도 및 탄생상수는 감소하였다. 높은 가교밀도 및 탄성상수는 카본블랙 첨가량에 관계없이 촉진제에 대한 황 비율 0.73 (${\fallingdotseq}1$)에서 나타났으며, 스코치시간 ($t_5$)은 촉진제에 대한 황 비율 변화에 거의 영향을 받지 않는 것으로 나타났다. 빠른 최적가황시간 ($t_{90}$) 역시 촉진재에 대한 황 비율이 1에 가까운 조건 (=0.73)에서 나타났다. 가황조건별 배합고무의 등가 가황곡선계수는 카본블랙 첨가량에 관계없이 CC 시스템에 대해서는 0.96, SEC 및 EC 시스템에 대해서는 0.74로 나타났다. 한편 가황고무의 마모된 부피는 부과된 하중이 증가함에 따라 지수적으로 증가하였다.

• 한국염색가공학회지
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• 제22권2호
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• pp.94-100
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• 2010

Colored compounds adsorption from the textile dyeing effluents on activated carbons produced from various indigenous vegetable sources by zinc chloride activation is studied. The most important parameters in chemical activation were found to be the chemical ratio of $ZnCl_2$ to feed (3:1), carbonization temperature (460-470 $^{\circ}C$) and time of activation (75 min). The absorbance at 511 nm (red effluent) and 615 nm (blue effluent) are used for estimation of color. It is established that at optimum temperature ($50^{\circ}C$), time of contact (30-40 min) and adsorbent loading (2 g/L), activated carbons developed from rain tree (Samanea saman) saw dust and blackberry (Randia formosa) tree saw dust showed great capability to remove color materials from the effluents. It is observed that adsorption of reactive dyes by all types of activated carbons is more than that of disperse dyes. It is explained that because of its acidic nature the activated carbon can adsorb better reactive dye particles containing large number of nitrogen sites and $-SO_3Na$ group in their structure. The use of activated carbons from the indigenous biomass would be economical, because saw dusts are readily available waste worldwide.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2011년도 춘계학술대회 초록집
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• pp.94.2-94.2
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• 2011

In this work, multi-functional groups, i.e., nitrogen and oxygen, contained microporous carbons (MF-MCs) were prepared by the one step carbonization of the poly(vinylidene chloride-co-acrylonitrile-co-methyl methacryalte) (PVDC-AN-MMA) without activation. The electrochemical performance of MF-MCs was investigated as a function of carbonization temperature. It was found that MF-MCs had a high specific surface area over $800m^2/g$ without additional activation, resulting from the micropore's formation by the release of chlorine groups. In addition, although functional groups decreased, specific surface area was increased with increasing carbonization temperature, leading to the enhanced electrochemical performance. The pore size of the carbon distributed mainly in small micropore of 1.5 to 2 nm, which was idal for aqueous electrolyte. Indeed, the unique microstructure features, i.e. high specific surface area and optimized pore size provided high energy storage capability of MF-MCs. These results indicated that the microporous features of MF-MCs lead to feasible electron transfer during charge/discharge duration and the presence of nitrogen and oxygen groups on the MF-MCs electrode led to a pseudocapacitive reaction.

• Bulletin of the Korean Chemical Society
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• 제21권6호
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• pp.571-576
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• 2000

Electrocatalytic effects for the reduction of thionyl chloride in $LiAICI_4/SOCl_2$ electrolyte solution containing Schiff base M(II) (M; Co and Fe) complexes are evaluated by determining kinetic parameters with cyclic voltammetry and chronoamperometry at a glassy carbon electrode. The charge transfer process during the reduction of thionyl chloride is affected by the concentration of the catalyst. The catalytic effects are demonstrated from both a shift of the reduction potential for the thionyl chloride toward a more positive direction and an increase in peak currents. Catalytic effects are larger in thionyl chloride solutions containing the binuclear [M(II) $_2$ (TSBP)] complex rather than mononuclear [M(II)(BSDT)] complexes. Significant improvements in the cell performance have been noted in terms of both thermodynamics and activation energy for the thionyl chloride reduction. The activation energy calculated from the Arrhenius plots is 4.5-5.9 kcal/mole at bare glassy carbon electrodes. The activation energy calculated for the catalyst containing solution is 3.3-4.9 kcalmole, depending on whether the temperature is lowered or rasied.