• 한국화재소방학회논문지
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• 제20권3호
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• pp.96-100
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• 2006

소형선박의 기관실을 상사한 모형실에서 분말소화설비의 개발을 위한 화재시험을 수행하였다. 화재시험이 수행된 모형실은 $2.9m^3,\;4.5m^3,\;8m^3$ 3종류였으며 각 모형실에는 개구부와 송풍용 팬이 설치되었다. 경유를 소화모형의 연료로 사용하였다. 또한 소화약제 방출용 노즐은 천장에서는 하향으로 벽 또는 벽의 모서리에서는 수평으로 분사되도록 설치하였다. 개발제품은 모든 소화모형을 분말소화약제 방출 중에 소화하였으며 소화 후 재발화가 없었다.

• 한국세라믹학회지
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• 제35권5호
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• pp.443-450
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• 1998

Layered double hydroxides(LDHs) [{{{{ {Mg }_{1-x } }}{{{{ {Al }_{x } }}({{{{ {OH}_{2 } }})]ζ+({{{{ {CO }`_{3 } ^{2- } ){ }_{x/2 } }}$.${{{{ { yH}_{2 }O }} wioth variation of layer charge densitywere synthesized by co-precipitation methdo since their charge densities have a very important role to be det-ermined the physicochemical properties of layered materials. The XRD IR and thermal studies of them were discussed and the kinetic study for the decarbonation reaction was also carried out. From the results of XRD analysis we found that the lattice parameter and the unit cell volume were linearly decreased with the amount of Al substituents(x) in the vicinity of x=2∼10${\times}$1/3${\times}$10-1 but they had nearly constant values when the x are far from these vicinit. The activation energies for the decarbonation reaction of x=6.8, 10${\times}$1/3${\times}${{{{ { 10}^{-1 } }} were estimated to be 47.0, 37.6, 39.3 kcal/mol The specific surface areas(90-120 m2/g) of stable hy-drotalcite-type LDHs were dractically decreased with increasing of layer charge density.

• 한국대기환경학회지
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• 제31권6호
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• pp.538-547
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• 2015

Test activated carbon fiber (ACF) was prepared from Polyacrylonirile (PAN) through oxidation and chemical activation. Immersion of ACF precursors in the aqueous KOH solution enhanced the surface structure, as examined by BET pore analysis. Specific surface area increased greatly from less than $70m^2/g$ to $1226m^2/g$ with 4 M KOH, and total pore volume also rose up to $0.483cm^3/g$. In particular, it was found that micropores favorable for $CO_2$ molecule capture occupied more than 95%. Maximum $CO_2$ adsorption capacity was 3.59 mmol/g at 298 K. Low depth of pores in the present ACF may facilitate the molecules' desorption for its regeneration.

• 한국정보디스플레이학회:학술대회논문집
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• 한국정보디스플레이학회 2002년도 International Meeting on Information Display
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• pp.526-529
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• 2002

Various fluoride films on a glass substrate were prepared and characterized in order to determine the best seed layer for a microcrystalline silicon (${\mu}c$-Si) film growth. Among the various group-IIA-fluoride systems, the $CaF_2$films on glass substrates illustrated (220) preferential orientation and a lattice mismatch of less than 0.7% with Si. $CaF_2$ films exhibited a dielectric constant between $4.1{\sim}5.2$ and an interface trap density ($D_{it}$ as low as $1.8{\times}10^{11}\;cm^{-2}eV^1$. Using the $CaF_2$/glass structure, we were able to achieve an improved ${\mu}c$-Si film at a process temperature of 300 $^{\circ}C$. We have achieved the ${\mu}c$-Si films with a crystalline volume fraction of 65%, a grain size of 700 ${\AA}$, and an activation energy of 0.49 eV.

• 한국방사성폐기물학회:학술대회논문집
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• 한국방사성폐기물학회 2003년도 가을 학술논문집
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• pp.158-161
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• 2003

중수로형 원전의 감속재 상층기체에 포함되어 원전 주변 대기로 방출되는 방사성이산화탄소$(^14CO_2)$를 효과적으로 흡착하여 분리, 고정할 수 있는 고효율 흡착제를 개발하기 위해, 활성탄 및 활성탄섬유에 금속수산화물(LiOH)을 담지한 몇 가지의 흡착제를 대상으로 XRD, BET, SEM/EDX 분석을 수행하였으며, 이산화탄소 흡착 성능을 시험하였다. 성능 시험 결과, 활성탄과 LiOH를 물리적으로 혼합한 시료가 함침법으로 LiOH를 활성탄에 담지한 시료에 비해 흡착 성능이 우수함을 알 수 있었으며, 활성탄의 표면을 개질한 결과 1N 질산으로 처리하였을 때에도 흡착성능이 향상됨을 확인하였다.

• 공업화학
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• 제28권1호
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• pp.8-16
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• 2017

에너지 저장 및 환경 관련 분야에 응용 흡착매질로 바이오매스 기반 활성탄의 중요성을 살펴보았다. 지금까지 발표된 연구 결과는 바이오매스 기반 활성탄의 표면적과 기공부피 이외에 이들의 표면 화학 특성 또한 다양한 분야에 응용될 수 있는 중요한 역할이 있음이 확인된다. 바이오매스 기반 활성탄의 용량은 바이오매스의 특성 및 이들의 활성화 공정에 따라 달라지므로 다양한 응용 분야에 맞게 제조할 수 있다. 따라서 본 리뷰에서는 다양한 분야에 이용되고 있는 바이오매스 기반 활성탄의 역할을 정리하였다.

• 한국식품과학회지
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• 제15권3호
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• pp.220-224
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• 1983

겉보리(올보리와 강보리) 및 쌀보리(세도하다가와 백동)를 각각 40 및 30%도정한 다음, 20, 30 및 $40^{\circ}C$에서 6시간 침지하면서 수화속도를 검토하였다. 수화속도는 수화시간의 평방근에 비례하였고, 확산계수 ($D,\;cm^{2}/min$)는 D = $D_{0}\;{\exp}\;(-E_{a}/RT)$로 표시되었다. 확산계수 값은 강보리가 돌보리보다 다소 높았으며, 세도하다가와 백동은 비슷하였다. 쌀보리의 확산계수는 겉보리보다 다소 높았다.

• Transactions on Electrical and Electronic Materials
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• 제16권4호
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• pp.194-197
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• 2015

La_9.33(Si₅V₁)O₂₆ ceramics were fabricated by the mixed oxide method for solid oxide electrolytes. La_9.33(Si₅V₁)O₂₆ specimens showed the hexagonal, space group P63 or P63/m, and the unit cell volume increased when the sintering temperature increased. The specimen sintered at 1,400℃ showed the X-ray patterns of the homogeneous apatite single phase without the second phase, such as La₂SiO₅ and SiO₂. The specimen sintered at 1,400℃ showed the maximum sintered density of 4.93 g/cm³. When the sintering temperature increased, the electrical conductivities increased, the activation energy decreased and the values were 7.83×10⁻⁴ S/cm, 1.61 eV at 600℃, respectively.

• Carbon letters
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• 제6권2호
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• pp.89-95
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• 2005

Crushed peach stone shells were impregnated with $H_3PO_4$ of increasing concentrations (30-70%) followed by heat treatment at 773 K for 3 h. Produced carbons (ACs) were characterized by $N_2$ adsorption at 77 K using the BET-equation and the ${\alpha}$-method. High surface area microporous ACs were obtained, with enhanced internal pore volume, as function of % $H_3PO_4$. Adsorption isotherms from aqueous solution were determined for methylene blue (MB) and p-nitrophenol (PNP), as representatives for dye and phenolics pollutant molecules. Application of the Langmuir model proved the high limiting capacity towards both solute molecules, MB was uptaken in increasing amounts as function of $H_3PO_4$ concentration and generated porosity. High removal of PNP was almost the same irrespective of porosity characteristics. Competitive adsorption of $H_2O$ molecules on the hydrophilic carbon surface seems to partially reduce the available area to the PNP molecules. Application of the pseudo-second order law described well the fast adsorption (${\leq}$ 120 min) at two initial dye concentrations.

• Carbon letters
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• 제7권1호
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• pp.1-8
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• 2006

The activated carbon "C" was obtained by carbonization followed by activation with steam at 40% of burn-off. Oxidized carbons C-N, C-P and C-H were obtained by oxidizing the activated carbon C with concentrated nitric acid, ammonium peroxysulfate and hydrogen peroxide, respectively. The textural properties of the carbons were determined from nitrogen adsorption at 77 K. The acidic surface functional groups were determined by pH titration, base neutralization capacity and electrophoretic mobility measurements. The cation exchange capacities of un-oxidized and oxidized carbons were determined by the removal of Cu(II) and Ni(II) from their aqueous solutions. The surface area and the total pore volume decreased but the pore radius increased by the treatment of activated carbon with oxidizing agents. These changes were more pronounced in case of oxidation with $HNO_3$. The surface pH of un-oxidized carbon was basic whereas those of the oxidized derivative were acidic. The removal of Cu(II) and Ni(II) was pH dependent and the maximum removal of the both ions was obtained at pH of 5-6. Cu(II) was more adsorbed, a phenomenon which was ascribed to its particular electronic configuration.