• 대한환경공학회지
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• 제39권1호
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• pp.34-39
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• 2017

현재까지 에너지의 지속적인 요구는 대부분 화석연료에 의해 충족되고 있다. 하지만 화석연료의 한계성과 온실가스 발생 등의 환경문제로 인해 새로운 대체에너지 연구 개발에 대한 관심이 크다. 탈수 하수 슬러지를 연료 에너지로 전환하기 위해 슬러지 촤와 흑연의 두 가지 열수용체를 적용한 경우 마이크로웨이브 열분해 특성을 파악하였다. 두 수용체 모두 열분해 생성물 발생량은 가스, 슬러지 촤 그리고 타르 순으로 생성되었다. 열분해의 경우 생성가스의 주성분은 수소와 메탄이고 일부 경질 탄화수소 등이 포함되었다. 흑연 수용체의 경우 중질타르가 다량 발생되었고, 많은 양의 경질탄화수소가 발생되었다. 이 상의 실험결과로 볼 때 탈수 하수 슬러지의 마이크로웨이브 열분해에 의해 생성된 가스를 연료로 이용이 가능하지만, 가스 중에 함유된 응축성 PAH 타르를 처리해야 한다.

• 한국대기환경학회지
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• 제19권4호
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• pp.437-449
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• 2003

A multi-functional indoor smog chamber was designed and evaluated to investigate photochemical or water vapor reaction mechanisms of air pollutants. Various smog chamber experiments could be conducted using ambient air or purified air in this smog chamber. The smog chamber consisted of a housing, a Teflon bag, blacklights, injection ports, sampling ports, and utility facilities. The characteristics of light source, the wall losses of air pollutants, and the quality of purified air were experimentally investigated. The maximum NO$_2$ photolysis rate was 1.10 min$^{-1}$ . In a 2.5-m$^3$ Teflon bag, the wall losses of ambient $O_3$, NO, and NO$_2$ were 1.2~2.4$\times$10$^{-3}$ min$^{-1}$ , 0.7~2.0$\times$10$^{-3}$ min$^{-1}$ , and 0.4~2.0$\times$10$^{-3}$ min$^{-1}$ , respectively. The wall loss of ambient particles ranging 0.05 to 0.2 ${\mu}{\textrm}{m}$ was 1.8~5.4$\times$10$^{-3}$ min$^{-1}$ , which was slightly higher than those of ambient gaseous species. The purified air supply system provided high quality of air with NO$_{x}$ < 1 ppb, and total hydrocarbons < 5 ppb.b.

• 천문학논총
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• 제32권1호
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• pp.25-27
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• 2017

We are creating all-sky diffuse maps from the AKARI mid-infrared survey data with the two photometric bands centered at wavelengths of 9 and $18{\mu}m$. The AKARI mid-infrared diffuse maps achieve higher spatial resolution and higher sensitivity than the IRAS maps. In particular, the $9{\mu}m$ data are unique resources as an all-sky tracer of the emission of polycyclic aromatic hydrocarbons (PAHs). However, the original data suffer many artifacts. Thus, we have been developing correction methods. Among them, we have recently improved correction methods for the non-linearity and the reset anomaly of the detector response. These corrections successfully reduce the artifact level down to $0.1MJy\;sr^{-1}$ on average, which is essential for discussion on faint extended emission (e.g., the Galactic PAH emission). We have also made progress in the subtraction of the scattered light caused in the camera optics. We plan to release the improved diffuse maps to the public within a year.

• Asian Journal of Atmospheric Environment
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• 제11권4호
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• pp.217-234
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• 2017

Indoor air pollutants can cause severe health problems, specifically in terms of toxicological impacts on human. Every day, a complex mixture of many air pollutants is emitted from various sources and subject to atmospheric processes that can create varied classes of pollutants such as carboxylic acids, aldehydes, ketones, peroxyacetyl nitrate, and hydrocarbons. To adhere to indoor air quality standards, a number of techniques such as photocatalytic oxidation of various volatile organic compounds (VOCs) have been employed. Among these techniques, titania ($TiO_2$) based photocatalytic reactions have proven to be the best benchmark standard approach in the field of environmental applications. Over the last 45 years, $TiO_2$-based photocatalytic reactions have been explored for the degradation of various pollutants. This review discusses the indoor air quality profile, types of indoor pollutants, available indoor air cleaning approaches, and performance of $TiO_2$-based catalysts. Finally, we have presented the perspectives on the progress of $TiO_2$ induced photocatalysis for the purification of indoor air.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2009년도 추계학술대회 논문집
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• pp.321-324
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• 2009

Upgrading of pyrolysis wax oil has been conducted in a continuous fixed bed reactor at $450^{\circ}C$, 1hour, LHSV 3.5/h. The catalytic degradation using HZSM-5 catalyst are compared with the thermal degradation and also was studied with a function of experimental variables. The raw pyrolysis wax oil shows relatively high boiling point distribution ranging from around $300^{\circ}C$ to $550^{\circ}C$, which has considerably higher boiling point distribution than that of commercial diesel. The product characteristic from thermal degradation shows a similar trend with that of raw pyrolysis wax oil. This means the thermal degradation of pyrolysis wax oil at high degradation temperature is not sufficiently occurred. On the other hand, the catalytic degradation using HZSM-5 catalyst relative to the thermal degradation shows the high conversion of pyrolysis wax oil to light hydrocarbons. This liquid product shows high gasoline range fraction as around 90% fraction and considerably high aromatic fraction in liquid product. Also, in the catalytic degradation the experimental variable such as catalyst amount and reaction temperature was studied.

• Bulletin of the Korean Chemical Society
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• 제28권8호
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• pp.1305-1310
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• 2007

A conjugated spirocyclic polymer was synthesized via the cyclopolymerization of 1,1-dipropargyl-1- silacyclohexane with various transition metal catalysts. The monomer, 1,1-dipropargyl-1-silacyclohexane was synthesized by Grignard reaction of 1,1-dichloro-1-silacyclohexane with propargyl magnesium bromide. This polymerization proceeded well to give the corresponding poly(1,1-dipropargyl-1-silacyclohexane). The catalytic activity of WCl6 was found to be similar with that of MoCl5. The structure of polymer having the conjugated backbone with silacyclohexane moieties was characterized by such instrumental methods as NMR (1H-, 13C-), IR, and UV-visible spectroscopies. The resulting polymers were mostly yellow or light-brown powders, depending on the catalyst systems used. This polymer was completely soluble in halogenated and aromatic hydrocarbons such as chloroform, 1,2-dichloromethane, benzene, toluene, and chlorobenzene, etc. The thermal and oxidative stabilities of polymer were also studied and discussed.

• 청정기술
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• 제16권3호
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• pp.198-205
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• 2010

염화탄화수소 열분해와 생성물분포 특성을 고찰하기 위해 등온 관형 반응기를 이용해 두 가지 실험을 수행하였다. 첫 번째는 반응분위기에 따른 열분해 특성을 파악하기 위해 $H_2$ 또는 Ar 반응분위기에서 dichloromethane ($CH_2Cl_2$) 분해율과 생성물분포 특성을 고찰하였다. Ar 반응분위기($CH_2Cl_2$/Ar 반응계)에서 보다 $H_2$ 반응분위기($CH_2Cl_2/H_2$ 반응계)에서 $CH_2Cl_2$ 분해율이 더 높았다. 이는 반응성 기체인 $H_2$ 분위기에서 $CH_2Cl_2$ 분해를 촉진시키며 수소 첨가 탈염소반응을 통해 탈염소화된 탄화수소화합물을 생성시키며, 다환방향족탄화수소 (polycyclic aromatic hydrocarbon: PAH)와 soot 생성을 억제하기 때문이다. $CH_2Cl_2/H_2$ 반응계에서 주요생성물로 탈염소화합물인 $CH_3Cl,\;CH_4,\;C_2H_6,\;C_2H_4,\;HCl$ 등이 생성되었으며, 미량 생성물로 chloroethylene이 검출되었다. $CH_2Cl_2$/Ar 반응계에서는 탄소물질수지가 낮았으며 특히 반응온도 $750^{\circ}C$ 이상에서 탄소물질 수지가 더 낮게 나타났다. 주요 생성물로는 chloroethylene과 HCl이 검출되었으며, 미량 생성물로는 $CH_3Cl$과 $C_2H_2$이 검출되었다. 고온 Ar 반응분위기에서 $CH_4$ 주입에 따른 chloroform($CHCl_3$) 분해와 생성물분포 특성을 비교 고찰하였다. $CHCl_3$ 분해율을 비교해 보면 $CH_4$을 주입할 경우($CHCl_3/CH_4/Ar$ 반응계)가 $CH_4$을 주입하지 않았을 경우($CHCl_3$/Ar 반응계)보다 분해율이 낮았다. 이는 $CHCl_3$가 분해되면서 생성되는 활성도가 큰 이중라디칼(diradical)인 :$CCl_2$가 첨가물로 주입된 $CH_4$와 반응하여 소모됨으로써 $CHCl_3$ 분해율이 상대적으로 감소되기 때문이다. Ar 반응분위기에서 $CH_4$ 첨가 여부에 따라 $CHCl_3$이 분해되면서 생성되는 생성물 분포는 큰 차이를 나타내고 있었다. 앞에서 고찰된 각 반응계에서 분해율 비교와 생성물 분포특성을 고려하고 열화학이론 및 반응속도론을 기초로 주요 반응경로를 제시하였다.

• Korean Chemical Engineering Research
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• 제45권2호
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• pp.117-123
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• 2007

농업용 필름을 제조하는데 사용되는 EVA 공중합체, LDPE, LLDPE 혼합물의 접촉 열분해 반응에 있어서 MCM-41 촉매에 aluminium을 첨가가 생성물의 수율, 탄소 수 분포 등에 미치는 영향을 조사하였다. Aluminium은 direct 및 post 방법으로 첨가하였고, 열분해 반응은 액상 접촉과 기상 접촉 반응 결과를 비교하였다. Direct 또는 post 방법으로 aluminium이 첨가된 MCM-41에서 aluminium 첨가량이 증가할수록 Lewis 산점이 증가하여 전체 산점의 양이 증가하였는데 post 방법으로 제조된 촉매에서 산점의 양이 더 많이 증가하였다. 액상 접촉 반응에서 aluminium의 양이 증가하면 가벼운 탄화수소가 많이 생기는데, $C_5-C_{12}$ 범위의 탄소화합물의 생성에 Al-MCM-41-P 촉매가 더 효과가 컸다. 기상 접촉 반응에서는 Al-MCM-41-D와 Al-MCM-41-P사이의 차이가 액상 접촉 반응시보다 상대적으로 적게 나타났으나, 액상접촉 반응에 비해 $C_{13}-C_{32}$ 범위의 탄화수소가 크게 감소했음을 알 수 있다.

• Asian Journal of Atmospheric Environment
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• 제6권2호
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• pp.96-103
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• 2012

Ambient particulate matter (PM) and particle-bound polycyclic aromatic hydrocarbon (PAH) concentrations were measured continuously for 70 days at a Korean elementary school located near a highway. The $PM_{10}$, $PM_{2.5}$, and $PM_1$ values were measured with a light-scattering, multi-channel, aerosol spectrometer (Grimm, Model 1.107). The number concentrations of the particles were measured using a scanning mobility particle sizer and counter (SMPS+C) which counted particles from 11.1 to 1083.3 nm classified in 44 channels. Particle-bound PAHs were measured with a direct reading, photoelectric aerosol sensor. The daily $NO_2$, $SO_2$, and CO concentrations were obtained from a national air-monitoring station located near the school. The average concentrations of $PM_{10}$, $PM_{2.5}$, and $PM_1$ were 75.3, 59.3, and $52.1{\mu}g/m^3$, respectively. The average number concentration of the ultrafine particles (UFPs) was $46,307/cm^3$, and the averaged particle-bound PAHs concentration was $17.9ng/cm^3$ during the study period. The ambient UFP variation was strongly associated with traffic intensity, particularly peak concentrations during the traffic rush hours. Particles <100 nm corresponded to traffic-related pollutants, including PAHs. Additional longterm monitoring of ambient UFPs and high-resolution traffic measurements should be carried out in future studies. In addition, transient variations in the ambient particle concentration should be taken into consideration in epidemiology studies in order to examine the short-term health effects of urban UFPs.

• 한국자원리싸이클링학회:학술대회논문집
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• 한국자원리싸이클링학회 2005년도 추계정기총회 및 제26회 학술발표대회 고분자리싸이클링기술 특별심포지엄
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• pp.75-82
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• 2005

바이오매스 열분해는 에너지와 가치있는 화학물질의 원료를 얻을 수 있는 유망한 방법 중의 하나이다. 열분해 반응기의 최적운전조건을 결정하기 위하여 기포유동층 반응기에서 상수리나무와 낙엽송의 열분해를 수행하였다. 온도, Uo/Umf, L/D가 생성물의 수율과 조성에 미치는 영향을 관찰하기 위하여 상수리나무와 낙엽송 톱밥으로 유동층 급속열분해를 수행하였다. 반응온도, Uo/Umf, L/D, 원료주입량의 효과를 결정하였고, 최적조건은 다음과 같다 : $T\;=\;400^{\circ}C,\;U_o/U_{mf}\;=\;3.0,\;L/D\;=\;2.0$. 바이오오일의 최대 수율은 약 55%이었고, 주요 조성은 carbohydrate류, guaiacol류, furan류, phenol류, syringol류 화합물이었다. 생성가스는 CO, $CO_2$, 저분자 탄화수소이었고, 조성을 이용하여 측정한 가스수율은 계산치와 일치하였다.