• 한국염색가공학회지
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• 제14권6호
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• pp.305-312
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• 2002

In order to give a silk-like touch to PET fabrics, the PET fabrics were treated with NaOH alkaline solution in various conditions. In alkaline treatment, the liquor flow type pilot weight reduction apparatus with magnetostrictive ultrasonic transducer was used for the study. The effects of ultrasonic application, treatment time and temperature at NaOH 4% and 6"A solution on the decomposition rate of PET fabrics. From the results of the decomposition rate of PET fabrics, the qualitative and quantitative analysis of oligomer after decomposition of PET fabrics carried out by the HPLC. On the other hand, the surface pore characteristics of decomposition PET fabrics measured by porosimetery. The pore characteristics on the surface of treated PET fiber depended on the decomposition rate and did not depend on the ultrasonic cavitation. The pore diameter of alkaline untreated PET fiber were 15A and those of treated PET fibers were 5~6$\AA$ at the maximum pore volume. The average pore sizes of fiber before and after treatment were 141 h and 160h, respectively. Total amount of oligomer of the untreated PET fibers were 1.70wt% and 67.7% of total oligomer occupied with PET cyclic trimer and PET cyclic tetramer. Total amount of oligomer of fiber with 26.9% and 48.0% of weight loss without ultrasonic application were 1.78wt% and 1.79wt%, respectively. Also total amount oligomer of fibers which were reduced 27.7% and 48.2% of weight loss with ultrasonic application were 1.74wt%. This result showed that the removal rate of oligomer in the process of alkaline hydrolysis with ultrasonic higher than that of without ultrasonic application.tion.

• 한국추진공학회:학술대회논문집
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• 한국추진공학회 1996년도 제7회 학술강연회논문집
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• pp.137-144
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• 1996

내열 복합 재료에 사용되는 경화된 페놀 수지(DURITE SC-1008)의 열분해 상수를 알아보기 위하여 Henderson and Freidman 분석법을 이용하여 반응 속도 상수를 구하였다. 가열 속도는 5,10, $20^{\circ}C$/min으로 변화 시켰으며 각각의 중량 감소 곡선으로부터 속도 상수 값을 구하였다. 열분해 반응은 크게 두 구간으로 나누어 진행되었으며 이러한 반응을 모사하기 위하여 반응 구간에 따른 속도 상수 값을 구하였다. 또한 실험 상수 값의 정확성을 확인하기 위하여 이론 열중량 곡선식을 직접 유도하여 상수 값을 대입한 결과 그 차이는 상관 계수가 1.19로써 실제 실험 값과 이론식에서 얻어진 값이 거의 일치되었다 그러므로 열분해 반응을 모사하기 위해서는 변화된 가열 속도에 따라서 중량 감소량을 구한 후 열분해 반응 구간을 분리하여 반응 상수론 구하는 것이 필요하다.

• The Korean Journal of Ecology
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• 제25권1호
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• pp.41-44
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• 2002

Weight loss, N and P dynamics during decomposition of fine roots (<2mm) of alder(Alnus japonica), oak (Quercus acutissima) and pitch pine(Pinus rigida) were studied for 33 months in Kongju, Korea. After 33 months, remaining weight of fine roots of alder, oak and pitch pine was 29.2%, 47.7% and 53.4% of the initial weight, respectively. The decomposition rate constant (k) for alder, oak and pitch pine was 0.448 $yr^1$, 0.269 $yr^1$, 0.228 $yr^1$, respectively. Initial concentration of N and P in fine roots was 10.32mg/g and 0.69mg/g for alder, 6.20mg/g and 0.37mg/g for oak and 7.26mg/g and 0.44mg/g for pitch pine, respectively. Initial concentration of N and P in alder were higher than those in oak and pitch pine. After 33 months, remaining N and P in fine roots was 39.5$\%$ and 31.8$\%$ for alder, 59.4$\%$ and 57.8$\%$ for oak, 63.0$\%$ and 83.4$\%$ for pitch pine, respectively. Decomposition rate and the rate of N released from decomposing fine roots was positively correlated with the initial N concentration of the fine roots.

• 한국재료학회지
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• 제14권6호
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• pp.407-412
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• 2004

Photo decomposition of gas phase benzene by $TiO_2$ thin films chemically deposited on alumina balls were investigated under UV irradiation. Photo decomposition rates were measured in real time during the reaction using a photo ionization detector, which ionizes C-H bonding of benzene molecules and then converts into volatile organic compounds (VOCs) concentrations. From the measuring results, the VOCs concentration increased instantly when IN irradiated because C-H bonds of benzene molecules strongly absorbed on the surface of $TiO_2$ films before the IN irradiation was destroyed by photo decomposition. After that, the VOCs concentration decreased with increasing surface area of $TiO_2$ and reaction time under the IN irradiation. At the optimal conditions for the photo decomposition of gas phase benzene, the reaction rate of the photo decomposition for high concentrations (over 60 ppm) was slow but that of relatively low concentration (under 60 ppm) was fast, due to limited surface area of $TiO_2$ thin films for the reaction. Thus, it is concluded that the photo decomposition rate was mainly affected by the surface area of $TiO_2$ or absorption reaction.

• 대한안전경영과학회:학술대회논문집
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• 대한안전경영과학회 2013년 춘계학술대회
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• pp.655-668
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• 2013

In this study, a combination of the plasma discharge in the reactor by the reaction surface discharge reactor complex catalytic reactor and air pollutants, hazardous gas SOx, change in frequency, residence time, and the thickness of the electrode, the addition of simulated composite catalyst composed of a variety of gases, including decomposition experiments were performed by varying the process parameters. 20W power consumption 10kHz frequency decomposition removal rate of 99% in the decomposition of sulfur oxides removal experiment that is attached to the titanium dioxide catalyst reactor experimental results than if you had more than 5% increase. If added to methane gas was added, the removal efficiency increased decomposition, the oxygen concentration increased with increasing degradation rate in the case of adding carbon dioxide decreased.

• 한국대기환경학회지
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• 제17권1호
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• pp.97-104
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• 2001

Decomposition of trichloroethlyene(TCE) in electron beam irradiation was examined on order to obtain information on the treatment of VOC in air. Air containing vaporized TCE has been studied in a flow reactor with different reaction environments, at various initial TCE concentration and in the presence and absence of water vapor. Maximum decomposition was observed in oxygen reaction environment and the degree of decomposition was about 99% at 20kGy for 2,000ppm initial TCE. The concentration of TCE exponentially decreased with dose in air and pure oxygen. The effect of water vapor on TCE decomposition efficiency was examined. The decomposition rate of TCE in the presence of water vapor (5,600 ppm) was approximately 10% higher than that in the absence of water vapor. Dichloroacetic acid, dichloroacethyl chloride and dichloroethyl ester acid were identified as primary products of this reaction adn were decomposed and oxidized to yield CO and $CO_2$. Perchloroethylene, hexachloroethane, chloroform and carbon tetrachloride were also observed as highly chlorinat-ed by products.

• 한국토양비료학회지
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• 제46권3호
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• pp.203-208
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• 2013

This study was conducted to investigate decomposition of livestock manure in soils cultivated with Chinese cabbage along an alitude gradient. The experiments were conducted in Kangreung (17 m above sea level), Bongpyeong (430 m above sea level), and Daekwanryeong (800 m above the sea level) in order to assess the decomposition rate and accumulations of livestock manures depending on different altitudes. During chinese cabbage cultivation, the decomposition ratios of organic matter derived form livestock manure expressed as % of the initial organic matter content were 42~48% for Kangreung, 26~29% for Bongpyeong and 10~14% for Daekwanryeong. Changes in air temperature with altitude might be a main factor affecting manure decomposition rates.

• 한국환경농학회지
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• 제20권3호
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• pp.135-142
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• 2001

가정에서 발생되는 퇴비화 가능한 폐기물 중 종이류 및 골판지 등을 제외한 것을 퇴비화 용기에 투입하기 전에 주방용 야채 분쇄기로 잘게 분쇄한 것(Case III)과 가정에서 비용을 들이지 않고 간단하게 실행할 수 있는 방법인 손으로 대충 찢는 것(Case II)으로 퇴비화하면서 분해율과 생산된 퇴비의 이${\cdot}$화학성을 조사하였다. 퇴비화과정 중 퇴비화용기의 습윤 및 건조 상태 잔류 퇴비화물질의 양에 대한 회귀직선식들은 각각 $R^2$ 값이 0.95 및 0.90 이상으로 이들 식들을 이용한 잔류 퇴비화물질의 양에 대한 예측이 가능하였다. 하루 전체 퇴비화물질의 무게 감소율은 Case II와 III의 경우 각각 6.82% 및 6.93%이었으나 투입된 퇴비화 가능한 가정 폐기물만에 대한 하루 무게 감소율은 56.43% 및 53.30%로 하루 전체 퇴비화물질의 무게 감소율보다 대단히 높았다. 하루 전체 퇴비화물질의 분해 율은 Case II와 III의 경우 각각 8.81% 및 7.70%이었으나 투입된 퇴비화 가능한 가정 폐기물만에 대한 하루 분해율은 각각 19.26% 및 22.95%로 주방용 야채 분쇄기로 거의 죽 상태로 분쇄하였을 경우(Case III) 분해율이 약간 높았다. 생산된 퇴비 중 이${\cdot}$화학적 특성은 Case II와 III의 경우 예상된 바와 같이 큰 차이는 없었다.

• 한국화재소방학회논문지
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• 제13권4호
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• pp.7-12
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• 1999

석유 화학플랜트에서 다량 부산되는 가연성 고체인 EVA(ethyl vinyl acetate) 분진의 열적특성 및 산화제와의 혼촉 위험성을 조사하였다. 시차주사열량계(DSC, Differential Scanning calorimeter) 및 열중량 분석기(TGA, Thermogavimetric Analysis)를 이용하여 온도에 따른 발열개시온도 및 중량감소를 조사하였고, EVA 분진의 위험성을 살펴보고자 몇 가지 대표적인 산화제와 혼합하여 무게비에 따른 압력용기 내에서의 혼촉 위험성을 조사하였다. DSC 분석 결과 EVA 분진의 열분해에 따른 발열 peak가 220~$250^{\circ}$ 부근에서 나타나고 있으며, TGA 분석결과 EVA 분진의 분해온도는 250~$500^{\circ}$ 범위이다. 압력 용기 시험에 의한 산화제와 EVA 분진의 혼촉 위험성은 오리피스 직경이 감소할수록 증가하며, 승온속도가 증가할수록 증가한다. 또한 승온속도가 느린 경우에는 시료의 분해온도와 산화제의 분해온도가 비슷한 경우 혼촉 위험성이 크게 나타났으며, 승온속도가 빠른 경우에는 시료 및 산화제의 분해온도보다는 분자 내에 산소의 함유량이 높은 산화제가 혼촉 위험성이 크게 나타났다.

• Elastomers and Composites
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• 제36권1호
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• pp.52-60
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• 2001

발포체의 물성은 발포체의 밀도, 사용된 폴리머의 기계적 물성과 열린 셀(open cell) 함량, 셀 크기, 셀 크기 분포, 셀 형태, 격벽의 두께 등을 포함하는 셀 구조에 의존하며 이러한 발포체의 밀도는 사용된 폴리머의 종류와 가교제의 농도, 발포제의 농도 그리고 가공 기술 및가공 조건 같은 다양한 원료물질과 가교조건에 영향을 받는다. Ethylene vinyl acetate coplymer (EVA) 발포체는 가교 발포체로서 가교속도와 발포제의 분해속도에 의해 발포특성에 영향을 받으며 이에 따라 발포체 물성에도 영향을 미친다. 본 연구에서는 가공 온도인 $155^{\circ}C$에서의 시간에 따른 발포제의 분해 속도 차이와 이에 따른 발포특성과 발포체의 물성에 대한 영향을 평가하였다. 발포제 분해 속도가 보다 느린 경우, 발포제 분해속도가 빠른 경우와 비교하여 낮은 밀도를 보여주었으며, 우수한 충격흡수성을 나타내었고 발포체의 셀 크기는 보다 균일하였다.