• Bulletin of the Korean Chemical Society
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• 제17권8호
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• pp.730-735
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• 1996

The layered perovskite oxide, KSr2Nb3O10, was synthesized. The interlayer potassium cations were readily exchanged by protons in hydrochloric acid solution to give the protonation compound, HSr2Nb3O10·0.5H2O. The intercalation compounds, [NH3(CH2)nNH3]xSr2Nb3O10, were also obtained by acid-base reactions between the protonation compound and organic bases, 1,n-alkyldiamines. The interlayer distances in the intercalation compounds were linearly increased with the increase of the number of carbon (Δc/Δn=1.05 Å) in 1,n-alkyldiamines. The intercalated alkyldiammonium ions formed a paraffin-like monolayer with average tilting angle (θ) of ca. 56°. The intercalation reactions occurred stoichiometrically. The thermal decomposition process of the intercalation compounds showed distinct three steps due to the desorption of hydrated water, the decomposition of organic moiety, and the decomposition of Sr-related compounds.

• Journal of Biosystems Engineering
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• 제21권1호
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• pp.84-93
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• 1996

Several paraffins(CnH2n +2) can be used as the thermal energy storage medium because of their large amount of latent heat and their flexibility of phase change temperature. But they have not been used in the thermal energy storage system because their long term stability have not been verified. Paraffins(CnH2n+2) which the values of n are 23, 24, 26 and 28 were selected for this experimental research. And this research was peformed to apply them to the practical systems. The results were summarized as follows. (1) The increase of phase change cycles had no effect on their phase change temperatures. (2) According as the values of n increased from 23 to 28, the specific heats of paraffins(CnH2n+2) increased, and were in the range of 0.47 0.75 ㎉/$kg^circ C$. (3) Thermal conductivities of them were in the range of 0.14 0.17 W/$m^circ C$. and specific gravities of them were in the range of 765800 kg/m3. (4) The density of paraffins was in the range of 765 800 kg/$m^circ C$ , and the density of solid phase was larger than that of liquid phase. (5) When the number of phase change cycles was 1, 500 cycles, the latent heat of paraffins was 90% of the initial value.

• 한국식품영양과학회지
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• 제27권2호
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• pp.252-258
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• 1998

Biosurfactant를 생산하는 미생물을 토양으로부터 분리하였다. 그 중에서 표면장력 및 계면장력 감소능에서 가장 우수한 L-417주를 순수분리하여 동정한 결과, No-Cardia속으로 판명되었다. Biosurfactant 생산을 위한 최적 배지조성은 3% n-hexadecane, 0.1% $NaNO_3$, 0.02% $K_2HPO_4$, 0.01% $KH_2PO_4$, 0.01% $MgSO_4 \;.\;7H_2O$, 0.01% $CaCl_2$ 0.02% yeast extract였으며, 최적 온도와 pH는 각각 $30^{\circ}C$와 6.0이였다. 이러한 조건에서 500ml용 shaking flask에 최적 배지 50ml를 넣어 배양했을 경우 대수증식기 말기인 4일째에 균의 증식과 유화활성이 가장 높게 나타남에 따라 Nocardia sp. L-417에 의한 bio-surfactant의 생산은 균의 생육과 밀접한 관련이 있는 것으로 판단된다. 이계면활성제는 산업적으로 널리 사용되는 bunker A, paraffin, corn oil 및 oilve oil 등에 대해서도 비교적 높은 유화활성을 나타내였다.

• 태양에너지
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• 제11권2호
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• pp.51-62
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• 1991

본 연구에서는 용융된 파라핀을 채운 수평 원관의 관벽을 냉각할 때에 관내에서 일어나는 열전달현상을 다루었다. 관내의 파라핀을 고상과 액상으로 구분하여 고상층에 대해서는 열전도 모델을, 그리고 액상층에 대해서는 자연대류를 고려한 열전달모델을 세워 수치해석하였고 이 과정에 대한 실험을 행하여 얻은 응고형태로부터 방열량을 계산하였다. 아울러 초기의 용융파라핀의 온도와 관벽의 냉각온도가 응고에 미치는 영향을 고찰하였다. 방열과정에서 액상파라핀의 응고속도를 결정하는 요인은 관벽의 냉각온도와 초기액상온도이나 대부분의 액상현열이 응고 초기에 급속히 방출되기 때문에 관벽의 냉각온도가 지배적인 요인으로 작용하였다. 따라서 방열과정에서의 열전달은 고상층 내의 열전도에 의해서 이루어지게 된다. 실험에서 관찰한 응고형태에서는 상부에 빈 공간이 발견되었다. 이는 초기 액상온도가 응고초기에 급속히 떨어짐으로써 온도에 따른 액상의 밀도차로 인해 생긴 것이다. 고 액간의 밀도차로 인한 수축현상은 응고과정의 전반에 걸쳐서 고르게 일어나므로 그 영향을 응고형태에서 구별하여 파악하기는 어려웠다. Fourier수와 고상의 Stefan수를 종속변수로 사용하면 관벽의 냉각온도와 초기액상온도에 무관하게 응고량을 단일곡선으로 표현할 수 있었다.

• International Journal of Air-Conditioning and Refrigeration
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• 제6권
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• pp.113-123
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• 1998

The present study is to investigate the effect of experimental parameters on the heat transfer characteristics of a spherical capsule storage system using paraffins. N-Tetradecane and mixture of n-Tetradecane 40% and n-Hexadecane 60% were used as paraffins. Water with inorganic material was also tested for the comparison. The experimental parameters were varied for the Reynolds number from 8 to 16 and for the inlet temperature from -7 to 2$^{\circ}C$. Measured local temperatures of spherical capsules in the storage tank were utilized to calculate charging and discharging times, dimensionless thermal storage amount, and the average heat transfer coefficients in the tank. Local charging and discharging times in the storage tank were significantly different. The effect of inlet temperature on charging time was larger than that on discharging time, but the effect of Reynolds number on charging time was smaller than that on discharging time. Charging time of paraffins was faster by 11~72% than that of water with inorganic material, but little difference of discharging time was found among them. The effect of Reynolds number on the dimensionless thermal storage was less during charging process and more during discharging process than the effect of inlet temperature. The effect of the inlet temperature and the Reynolds number on the average heat transfer coefficient of the storage tank was stronger during discharging process than during charging process. The average heat transfer coefficients of the spherical capsule system using paraffins were larger by 40% than those using water.

• 태양에너지
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• 제9권3호
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• pp.44-54
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• 1989

Heat transfer phenomena during inward melting process of the phase change material were studied experimentally. N-docosane paraffin [$C_{22}H_{46}$] is used for phase change material and its melting temperature is $42.5^{\circ}C$. Experiments were performed for melting of an initially no-sub cooled or subcooled solid in a horizontal cylinder, in order to compare and investigate the radial temperature distribution, ratio of melting and melted mass, various energy components stored from the cylinder wall, figure of the melting front in the horizontal cylinder. The solid-liquid interface motion during phase change was recorded photographically. The experimental results reaffirmed the dominant role played by the conduction at early stage, by the natural convection at longer time during inward melting in the horizontal cylinder. Ratio of melting and melted mass are more influenced by wall temperature, rather than by the initial temperature of solid. The latent energy is the largest contributor to the total stored energy.

• 한국에너지공학회:학술대회논문집
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• 한국에너지공학회 2010년도 춘계학술 발표회
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• pp.199-199
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• 2010

Polymeric membranes have been widely used to separate gas mixtures, such as $O_2/N_2,\;CO_2/CH_4,\;CO_2/N_2$, and olefin/paraffin. The permeation selectivity is the ratio between composition ratio at the permeate side and composition ratio at the feed side. In addition, the permeation selectivity is a product of solubility selectivity and diffusivity selectivity. We present a novel idea and describe its experimental result, which was achieved by preparing polymer gel films that included a room temperature ionic liquid (RTIL) in a polymer matrix. It is known that $CO_2$ can dissolve easily in imidazolium-based RTILs. We prepared polymer-ionic liquid gel films using an ionic liquid, 1-ethyl-3-methylimidazolium acetate ([emim] acetate, C-tri) and a host polymer, poly (vinyl acetate) (PVAc, Aldrich).

• 폴리머
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• 제35권4호
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• pp.363-369
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• 2011

콘크리트 제조 시 사용되는 잉여수를 지연 흡수시키기 위하여 역유화중합법으로 중합된 가교 poly(sodium acrvlate) (cPSA)를 ethylene glycol dimethacrylate(EGDMA)로 표면 가교시켰다. cPSA의 제조에서 연속상은 paraffin liquid, 단량제는 8 M 농도의 NaOH 수용액으로 90% 중화된 acrylic acid(AA), 가교제는 N,N-methylene bisacrylamide(MBA), redox 개시제는 ammonium persulfate(APS)와 sodium metabisulfite(SMBS)를 사용하여 역유화중합법으로 제조하였다. 제조된 cPSA는 EGDMA플 사용하여 표면 가교 반응을 수행하였다. 시멘트 수용액에서 $Ca^{2+}$ 이온과 cPSA의 상호 작용을 관찰하기 위하여 FTIR spectroscopy 분석법을 사용하였다. 제조된 흡수제들을 탈이온수 $Ca(OH)_2$ 수용액(pH 12) 및 시멘트 포화 수용액에서의 팽윤비를 측정하였으며, cPSA는 2시간만에 팽윤이 완료되었지만, 표면이 가교된 cPSA-EGDMA는 3시간 후 팽윤이 거의 완료되는 것을 관찰하였다. 또한 합성한 cPSA-EGDMA를 첨가함으로써 시멘트의 응결시간과 모르타르의 압축강도 증가를 관찰하였다.

• Korean Chemical Engineering Research
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• 제44권4호
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• pp.393-398
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• 2006

고농도의 1-부텐을 생산하기 위하여 흡착 분리제의 개발이 필수적인데, 본 연구에서는 메조포러스 실리케이트인 MCM-41을 지지체로 하여 $AgNO_3$를 함침시켜 흡착제를 제조한 후, 1-부텐과 n-부탄의 흡착 특성을 연구하였다. 또한, 열처리 조건에 따른 $Ag^+$ 이온의 형성 비율과 1-부텐의 결합 능력을 알아보았다. MCM-41 흡착제의 경우, 13X 제올라 이트에 비하여 매우 높은 흡착량을 보여주었으며, 은이 담지되었을 때, n-부탄의 흡착량은 감소하는 반면에 1-부텐의 흡착량은 증가함으로써 1-부텐과 n-부탄의 흡착 분리에 매우 좋은 성능을 갖음을 확인할 수 있었다. 또한, 진공 분위기에서 373 K로 열처리한 Ag/MCM-41의 경우 가장 높은 1-부텐/n-부탄 흡착비를 보였으며, 특히 저압에서 매우 높은흡착비를 보여주었다.

• 한국분말재료학회지
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• 제10권1호
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• pp.6-14
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• 2003

The purpose of the present study is to investigate the method decreasing debinding time as well as lowering operation condition than pure supercritical $CO_2$ debinding by using cosolvent or binary mixture of propane + $CO_2$. First method is to add cosolvent, such as n-hexane, DCM, methanol, 1-butanol, in supercritical $CO_2$. In case of adding cosolvent, we were found the addition of non-polar cosolvent (n-hexane) improves dramatically the binder removal rate (more than 2 times) compared with pure supercritical $CO_2$ debinding, second method is to use mixture of supercritical propane + $CO_2$, as solvent. In case of using mixture of supercritical propane + $CO_2$, the rate of debinding speeded up with increasing of pressure and concentration of propane at 348.15 K. It was found that addition of cosolvent (e.g., n-hexane, DCM) and binary mixture propane + $CO_2$ for supercritical solvent remarkably improved binder removal rate for the paraffin wax-based binder system, in comparison with using pure supercritical $CO_2$.