• 상하수도학회지
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• 제28권2호
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• pp.235-248
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• 2014

The widespread occurrence of dissolved endocrine disrupting compounds(EDCs) and pharmaceutical active compounds(PhACs) in water sources is of concern due to their adverse effects. To remove these chemicals, adsorption of EDCs/PhACs on granular activated carbon(GAC) was investigated, and bisphenol A, carbamazepine, diclofenac, ibuprofen, and sulfamethoxazole were selected as commonly occurring EDCs/PhACs in the aquatic environment. Various adsorption isotherms were applied to evaluate compatability with each adsorption in the condition of single-solute. Removal difference between individual and competitive adsorption were investigated from the physicochemical properties of each adsorbate. Hydrophobicity interaction was the main adsorption mechanism in the single-solute adsorption with order of maximum adsorption capacity as bisphenol A > carbamazepine > sulfamethoxazole > diclofenac > ibuprofen, while both hydrophobicity and molecular size play significant roles in competitive adsorption. Adsorption kinetic was also controled by hydrophobicity of each adsorbate resulting in higher hydrophobicity allowed faster adsorption on available adsorption site on GAC. EDCs/PhACs adsorption on GAC was determined as an endothermic reaction resulting in better adsorption at higher temperature ($40^{\circ}C$) than lower temperature ($10^{\circ}C$).

• 펄프종이기술
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• 제45권1호
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• pp.42-51
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• 2013

In this study, oil palm biomass such as empty fruit bunch (EFB) and palm kernel shell (PKS) was used as raw materials for making pellets. Hardwood sawdusts were also mixed with EFB and PKS for making pellets. For improving a bad forming behavior in a pelletizer, 1 to 3 per cent of corn starch based on oven-dried weight biomass was added. The starch contributed to the decrease of dust generation in addition to the improvement of forming capability during pellet forming. Heating values of every pellets made of EFB and PKS were higher than 4,300 kcal/kg for the first grade pellet, irrespective of addition of sawdusts. However, the pellets made of EFB and PKS had ash contents over 3 per cent, which made it impossible to be applied for home use. Instead, they could be applied for industrial use. For studying their combustion characteristics, the pellets from the mixtures of EFB, PKS and sawdusts were analyzed using thermal gravimetric analyzer (TGA). From the TGA results, thermal decomposition of EFB and PKS occurred following three including endothermic reaction and dehydration, devolatilization of the major chemical components, and finally combustion of residual lignin and char.

• 한국염색가공학회지
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• 제8권2호
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• pp.1-7
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• 1996

Thermotropic liquid-crystalline polyurethanes were synthesized by the polyaddition reaction of such para-substiuted diisocyanate monomer as 1,4-phenylene diisocyanate(1,4-PDI) and 2,5-tolylene diisocyanate(2,5-TDI), with 4,4'-bis($\omega$-hydroxyalkoxy)biphenyls(BPm: $HOC_{m}OC_{6}H_{4}C_{6}H_{4}OC_{m}H_{2m}OH$; m is the carbon number of the hydroxyalkoxy group). These polyurethanes have mesogenic biphenyl units in the main chain. Properties of polymers were studied by differential scanning calorimetry, wide-angle X-ray scattering, thermogravimetic analysis, polarizing microscopy, and infraed spectroscopy. DSC thermograms for these polymers exhibited two endothermic peaks corresponding to phase transitions of melting and isotropization. Mesomorphic behavior of the polyurethanes were also observed under the polarizing microscope. For example, polyurethane 2,5-YDI/BP5 with [$\theta$]=0.44 prepared from 2,5-TDI and BP5 exhibited a liquid crystalline phase from 194 to 205$^{\circ}C$. Infrared spectrum study indicated that the hydrogen bonding between urethane linkages affected the mesomorphism. The thermostabilities of polyurethanes 2,5-TDI/BP5 and 1,4-PDI/BP5 were measured at a heating rate of 1$0^{\circ}C$/min in air. The temperatures of 5% weight loss for 2,5-TDI/BP5 and 1,4-PDI/BP5 were 297 and 334$^{\circ}C$, respectively.

• 한국항공우주학회지
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• 제41권8호
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• pp.597-604
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• 2013

본 논문에서는 열분해 및 삭마 환경의 복합재 구조물에 대한 열기계적 연계 해석을 수행하였다. 열분해 과정의 재료 밀도 감소, 기공 가스 확산, 흡열 반응 에너지와 삭마 과정에서의 표면 침식 효과 등을 고려하였다. 상용 유한요소 코드에 교차 연계 알고리듬을 적용하여 완전 연계된 열 해석 및 구조 해석 인터페이스를 구성하였다. 수치 실험을 통해서 탄소/페놀릭 복합재료의 기본적인 열분해 및 삭마 특성을 분석하였다. 특히, 화학적 및 기계적 삭마에 영향을 미치는 주요 인자에 따른 표면 침식량 등을 비교하였다. 또한, 열분해 과정의 수축 또는 팽창 변형도가 재료의 열기계적 거동에 미치는 영향도 검토하였다.

• 한국응용과학기술학회지
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• 제20권3호
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• pp.230-236
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• 2003

Synthesis gas is commercially produced by a steam reforming process. However, the process is highly endothermic and energy-consuming. Thus, this study was conducted to produce synthesis gas by the partial oxidation of methane to decrease the energy cost. Supported Ni catalysts were prepared by the impregnation method. To examine the activity of the catalysts, a differential fixed bed reactor was used, and the reaction was carried out at $750{\sim}850^{\circ}C$ and 1 atm. The fresh and used catalysts were characterized by XRD, XPS, TGA and AAS. The highest catalytic activity was obtained with the 13wt% Ni/MgO catalyst, with which methane conversion was 81%, and $H_2$ and CO selectivities were 94% and 93%, respectively. 13wt% Ni/MgO catalyst showed the best $MgNiO_2$ solid solution state, which can explain the highest catalytic activity of the 13wt% Ni/MgO catalyst.

• 대한환경공학회지
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• 제37권11호
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• pp.642-648
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• 2015

수계에 존재하는 인산염의 흡착제거 용량을 향상시키기 위하여, 참나무 기반 활성탄을 제조하였으며, 이때 $Fe^{3+}$와 $Al^{3+}$이온의 혼합물을 흡착제 표면에 담지 하였다. 금속담지 활성탄의 인산염의 흡착용량은 금속이온으로 표면을 개질 하지 않은 활성탄에 비해 약 8배 높게 나타났다. 흡착평형량은 흡착반응의 온도가 증가할수록 증가하였으며, Langmuir 흡착등온식의 경향과 일치하였다. 제조된 금속담지 활성탄의 인산염 흡착제거공정은 흡열의 자발반응으로 진행되었음을 확인하였다. 흡착공정의 거동과 제거속도를 평가하기 위하여, 세공확산모델을 통해 내부 확산계수를 산출하였으며, 이는 실험결과와 매우 일치하였다.

• 한국응용과학기술학회지
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• 제21권3호
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• pp.225-230
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• 2004

Synthesis gas is a high valued compound as a basic chemicals at various chemical processes. Synthesis gas is mainly produced commercially by a steam reforming process. However, the process is highly endothermic so that the process is very energy-consuming process. Thus, this study was carried out to produce synthesis gas by the partial oxidation of methane to decrease the energy cost. The effects of reaction temperature and flow rate of reactants on the methane conversion, product selectivity, product ratio, and carbon deposition were investigated with 13wt% Ni/MgO catalyst in a fluidized bed reactor. With the fluidized bed reactor, $CH_4$ conversion was 91%, and Hz and CO selectivities were both 98% at 850$^{\circ}C$ and total flow rate of 100 mL/min. These values were higher than those of fixed bed reactor. From this result, we found that with the use of the fluidized bed reactor it was possible to avoid the disadvantage of fixed bed reactor (explosion) and increase the productivity of synthesis gas.

• 한국추진공학회:학술대회논문집
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• 한국추진공학회 2009년도 춘계학술대회 논문집
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• pp.155-158
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• 2009

본 연구에서는 Hydroxy Terminated Polyether(HTPE) 추진제 원료와 HTPE 둔감 추진제 조성 2종에 대하여 DSC와 TGA를 사용하여 열분해 특성을 고찰하였고, Extermely Insensitive Detonating Substance(EIDS) 완속가열 시험을 수행하여 반응 시간과 반응 온도를 측정하였다. AN이 포함된 HTPE 002는 약 $125^{\circ}C$에서 AN의 상전이과정($II{\rightarrow}I$)을 거친 후, 약 $200^{\circ}C$범위까지 BuNENA와 AN이 함께 발열특성을 가지고 분해됨을 알 수 있었다. EIDS 완속가열 시험을 수행한 결과 HTPE 001은 $250^{\circ}C$, HTPE 002는 $152^{\circ}C$ 부근에서 반응이 있어났으며, 두 추진제 모두 $115^{\circ}C$부근에서 급격한 온도 상승이 일어났다.

• 마이크로전자및패키징학회지
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• 제18권4호
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• pp.27-32
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• 2011

Tin(II) acetate와 tin(II) chloride의 주석 precursor를 사용하여 상온에서의 강제 환원 반응으로 주석 나노 입자를 합성시켰다. 0.015 g의 동일한 PVP 양을 첨가한 조건에서 PVP의 분자량이 클수록 비정상적으로 큰 입자들의 생성율이 증가되어 입도 범위가 매우 넓은 주석 나노 입자들이 생성됨을 확인할 수 있었다. 합성된 주석 나노 입자를 함유하는 DEG 용액의 DSC 분석 결과 1차 가열에서는 35 nm 미만 특정 크기 입자들의 수가 충분한 경우에서 DEG의 증발 흡열피크 외에도 특정 크기 입자들의 융점 강하 흡열 피크가 구분되게 검출되었다. 1차 DSC 측정 중 용융된 주석 나노 입자들은 서로 접촉하며 뭉쳐지는 현상이 발생하므로 2차 가열시에는 벌크 주석의 용융 피크에 해당하는 $232^{\circ}C$ 흡열 피크만이 관찰되었다.

• 한국지반공학회논문집
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• 제16권4호
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• pp.157-170
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• 2000

본 연구에서는 자연점토에 대한 구리 흡착 및 구리와 아연의 경쟁 흡착 시 온도변화에 따른 흙의 각 구성성분별 흡착거동을 살펴보기 위해 혼합 흡착-연속추출법(combined adsorption-sequential extraction analysis, CASA)을 사용하였다. 실험결과 중금속 아연의 경우 농도에 따른 차이는 있지만 온도증가에 따라 주로 이온교환 형태로 흡착되는 것을 알 수 있고, 구리와 경쟁흡착의 경우 이러한 경향은 더욱 커져서 약 80~90%정도가 이온교환형태로 흡착되어진다. 반면 구리의 경우 실험을 수행한 거의 모든 농도 범위에서 약 50%이상이 탄산염 형태로 흡착되어진다. 탄산염형태로의 흡착 양상은 단일 흡착의 경우 온도증가에 따라 약 5% 증가하는 경향을 보이고, 경쟁흡착의 경우에는 약 10%정도 증가하는 경향을 나타내었다. 그리고 자연점토에서의 아연과 구리의 각 구성성분 별 흡착거동은 이온 교환 형태로 분배되는 경우를 제외하고는 온도증가에 따라 흡착량이 증가하는 흡열반응$(\DeltaH0>0)$인 것으로 나타났다.