• 한국조명전기설비학회:학술대회논문집
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• 한국조명전기설비학회 2003년도 학술대회논문집
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• pp.133-137
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• 2003

When a light is projected upon a material, part of its radiation energy is absorbed and the rest is reflected or transmitted according to the nature of the material. The molecules of the substance absorbing a light obtains the radiation energy to the wavelength of the light to make photochemical degradation by ultraviolet ray or thermal reactions like physical damage by infrared ray. The degree of damage by radiation energy varies to the substances of materials, the spectral power distribution of the light source and the duration of irradiation. Because the damage brings about a devaluation of material and once damaged, it is irretrievable, it is necessary to minimize the damage and conserve the native quality of a material by a protective lighting system. A measuring system was set up to measure the temperature rise of each sample by infrared radiation from light sources. And the temperature rise and temperature distribution by various infrared lamps were measured with varying time.

• Bulletin of the Korean Chemical Society
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• 제17권6호
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• pp.506-510
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• 1996

The syntheses and photoreactions of haloarenes, in which the aryl and haloaryl moieties are tethered by a simple alkyl group, were studied. For 2-benzyl-1-halobenzene, in which two aryl moieties were connected by methylene group, photoreduced product, diphenylmethane, was obtained along with the minor formation of the photocyclized product, fluorene, in acetonitrile solvent. For 1-halo-2-phenethylbenzene, in which two aryl moieties were connected by ethylene group, photocyclized products, 9,10-dihydrophenanthrene and phenanthrene, were obtained along with the minor formation of photoreduced product, bibenzyl, in acetonitrile solvent. The photoreaction selectivities in several solvent systems were studied: In cyclohexane, 2-benzyl-1-chlorobenzene was photoreduced more effective than 2-benzyl-1-bromobenzene; In the presence of NaOH, 1-halo-2-phenethylbenzenes gave 9,10-dihydrophenanthrene and, in the presence of toluene, they gave phenanthrene. A radical reaction mechanism is proposed for the explanation of the reactions. This study shows that the photoreaction of haloarene, in which haloaryl and aryl moieties are tethered by ethylene group, can be used for ring formation of 9,10-dihydrophenanthrene otherwise difficultly accessible.

• 대한기관식도과학회지
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• 제15권1호
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• pp.60-63
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• 2009

The photodynamic therapy (PDT) is a new treatment modality of destroying malignant tumors and pre-malignant lesions based on the use of photodynamical damage to tumor cells under the photochemical reactions. But the clinical reports of photodynamic application on the benign tumor of the internal organs were extremely rare. So we decribed our experience of one case of benign tracheal tumor successfully treated by PDT.

• Journal of the Optical Society of Korea
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• 제17권1호
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• pp.73-80
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• 2013

In the process of lithography using ultra violet light sources for semiconductor devices, most of defects are made by sub-micrometer pollutants generated at photochemical reactions. We proposed and developed a novel vibration-insensitive on-axis interferometer with a sub-micrometer lateral resolution by using the interference between two beams: one scattered from defects and the other reflected from a reference area without defects. The proposed system was successfully demonstrated to detect a small Al defect of 0.5 ${\mu}m$ diameter within the inspection time of less than 30 minutes over the area of the photo-mask which is 6 inch by 6 inch square.

• Bulletin of the Korean Chemical Society
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• 제10권3호
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• pp.223-226
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• 1989

The chemical reactivity of 5,7-dimethoxycoumarine with adenosine has been calculated by the frontier electron and PPP-Cl MO methods. Results suggest that the major reactivity of the 5,7-dimethoxycoumarin is highest at the carbon-4 (position 4), whereas the electrophilic reactivity is generally spread all over the 5,7-dimethoxycoumarin molecule. These results are consistent with the experimental photoaddition reaction products. The small change of bond orders on excitation does not give enough reactivity to triplet states or the efficient intersystem crossing from $T_1\;to\;S_0$ inhibits photoaddition of 5,7-dimethoxycoumarine to adenosine. Although the relative intensity of the singlet band appears to be considerably higher than the triplet band intensity, its integrated intensity, i.e. oscillator strength, is comparable to that of the 5,7-dimethoxycoumarin and adenosine bands.

• Applied Biological Chemistry
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• 제17권3호
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• pp.149-176
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• 1974

팔종(八種)의 치환(置換) diphenyl ether 제초제(除草劑)를 Rayonet 광화학(光化學) 반응기(反應器)를 사용(使用)한 모조환경조건하(模造環境條件下)에서 용액상(溶液相) 광분해(光分解)시켜 그 분해산물(分解産物)에 관(關)하여 연구(硏究)하였다. 시료(試料)로 사용(使用)된 화합물(化合物)들은 300 nm에서 광화학반응(光化學反應)을 일으키기에 충분(充分)한 energy를 흡수(吸收)하였으며 분해산물(分解産物)은 tlc, glc, ir, ms, 그리고 nmr 등(等)에 의(依)하여 확인(確認)하였다. 그 결과(結果)를 요약(要約)하면 C-6989의 용액상(溶液相) 광분해(光分解) : p-nitrophenol이 다량(多量) 생성(生成)됨을 보아 ether결합(結合)의 결렬이 주반응(主反應)이며 치환기(置換基) $NO_2{\rightarrow}NH_2$의 광화학적(光化學約) 환원반응(還元反應)과 $CF_3{\rightarrow}COOH$의 산화반응(酸化反應)도 관찰되었다. p-Nitrophenol의 수중(水中) 광분해(光分解) : quinone(0.28%), hydroquinone(0.66%) 및 p-aminophenol(0.42%)과 비교적(比較的) 소량(少量)의 미지화합물(未知化合物)이 생성(生成)됨을 확인(確認)하였고 모화합물(母化化合物)은 대부분(大部分) 작용(作用)을 받지 않은 채로 존재(存在)하였다. 이들 분해산물(分解産物)의 형성기구(形成機構)는 $n{\rightarrow}{\pi}^*$ 및 여기(勵起)를 거친 nitro-nitrite재배열(再配列) 및 자유기(自由基)에 의(依)한 수소탈취(水素脫取)를 통(通)한 광환원(光還元)으로 추측(推測)되었다. Nitrofen의 용액상(溶液相) 광분해(光分解) : n-hexane중(中)에서는 $NO_2$기(基)의 광환원(光遷元)이 주반응(主反應)이었고 수용액(水溶液) 중(中)에서는 광환원(光遷元) 및 hydroxylation이 ether결합(結合) 결렬 보다 현저하였다. hydroxide ion에 의한 친핵적(親核的) 치환(置換), hydroxyl기(基) 및 소량(少量)이긴 하지만 수소(水素)에 의한 염소(鹽素)의 치환(置換)도 다소 관찰되었다. MO-338의 용액상(溶液相) 광분해(光分解) : n-hexane용액중(中) nitro기(基)의 광환원(光遷元) 반응(反應)과 수용액중(水溶液中)에서의 광환원(光遷元) 및 hydroxylation이 주반응(主反應)이었으며 hydroxyl기(基)와 수소(水素)에 의(依)한 염소(鹽素)의 치환(置換) 및 ether결합(結合)의 결렬도 볼 수 있었다. n-Hexane과 cyclohexane중(中)에서의 MC-4379, MC-3761, MC-5127, MC-6063 및 MC-7181의 광분해(光分解) : nitro기(基)의 광환원반응(光還元反應)과 수소(水素)에 의(依)한 halogen의 치환반응(置換反應)이 주(主)로 일어났다. MC-4379의 수중(水中) 광분해(光分解) : ether결합(結合)의 결렬, hydroxyl기(基)에 의한 carboxymethyl기(基)의 치환(置換), hydroxylation, hydroxyl기(基)에 의한 nitro기(基)의 치환(置換)이 주(主)로 일어났고 광환원(光還元) 및 광염소화반응(光鹽素化反應)도 약간 일어났다. MC-3761의 수중(水中) 광분해(光分解) : ether결합(結合)의 결렬, hydroxyl기(基)에 의한 carboxymethyl기(基)의 치환(置換) 및 hydroxylation이 수반되는 광환원(光還元)이 주반응(主反應)이었다. MC-5127의 수중(水中) 광분해(光分解) : 수소(水素)에 의한 carboxyethyl기(基)의 치환(置換)이 현저 하였고 ether결합(結合)의 결렬, 광환원(光還元) 및 탈염소화반응(脫鹽素化反應)도 약간 관찰되었으며 decarboxyethylation은 decarxy-methylation보다 용이함을 볼 수 있었다. MC-6063의 수중(水中) 광분해(光分解) : ether결합(結合)의 결렬과 탈염소화반응(脫鹽素化反應)이 주(主)로 관찰되었다. MC-7181의 수중(水中) 광분해(光分解) : 수소(水素)에 의한 carboxymethyl기(基)의 치환(置換)과 monodechlorination이 현저하였고 ether결합(結合) 결렬과 hydroxylation도 약간 일어났다. 3-Carboxymethyl-4-nitrophenol의 수중(水中) 광분해(光分解) : 방향족(芳香族) ester에서 흔히 볼 수 있는 광유도(光誘導) Fries rearrangement는 이 화합물(化合物)의 carboxymethyl기(基)에서는 볼 수 없었고 $nitro{\to}nitroso$반응(反應)이 주(主)로 일어났다.

• 한국대기환경학회지
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• 제27권3호
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• pp.281-290
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• 2011

In this study, a series of experiments were carried out to measure temporal stability of reduced sulfur compounds (RSCs) in Tedlar bag samples as a function of elapsed storage time. To this end, temporal variability of 4 RSC standard gases ($H_2S$, $CH_3SH$, DMS, DMDS) was measured up to 29 days. For the purpose of comparison, RSC samples were stored in both individual and mixed state. In the case of mixed standard, samples were also examined to allow comparison between light and dark condition. Then results of $CH_3SH$ data were the most stable with the least change in its concentrations through the end of exps (29 days). When compared with previous studies, the extent of stability appeared to be influenced by the initial concentration levels of samples. When the patterns were compared between individual and mixture samples, differences were not significant in the case of $H_2S$ and DMS. The effects of light conditions on temporal stability were seen to be fairly sensitive on most RSC other than $H_2S$. The results of our study confirm that the stability of RSC storage is affected by their involvement in photochemical reactions.

• Asian Journal of Atmospheric Environment
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• 제9권4호
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• pp.259-271
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• 2015

This study conducted analyses on biogenic volatile organic compounds (BVOC) emission sources contributing to urban ozone ($O_3$) concentration in Osaka Prefecture, Japan in summer 2010 by using the Weather Research and Forecasting model (WRF) version 3.5.1 and the Community Multiscale Air Quality model (CMAQ) version 5.0.1. This prefecture is characterized by highly urbanized area with small forest area. The contributions of source regions surrounding Osaka were estimated by comparing the baseline case and zero-out cases for BVOC emissions from each source region. The zero-out emission runs showed that the BVOC emissions substantially contributed to urban $O_3$ concentration in Osaka (10.3 ppb: 15.9% of mean daily maximum 1-h $O_3$ concentration) with day-by-day variations of contributing source regions, which were qualitatively explained by backward trajectory analyses. Although $O_3$ concentrations were especially high on 23 July and 2 August 2010, the contribution of BVOC on 23 July (35.4 ppb: 25.6% of daily maximum $O_3$) was much larger than that on 2 August (20.9 ppb: 14.2% of daily maximum $O_3$). To investigate this difference, additional zero-out cases for anthropogenic VOC (AVOC) emissions from Osaka and for VOC emissions on the target days were performed. On 23 July, the urban $O_3$ concentration in Osaka was dominantly increased by the transport from the northwestern region outside Osaka with large contribution of $O_3$ that was produced through BVOC reactions by the day before and was retained over the nocturnal boundary layer. On 2 August, the concentration was dominantly increased by the local photochemical production inside Osaka under weak wind condition with the particularly large contribution of AVOC emitted from Osaka on the day.

• 대한화학회지
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• 제30권2호
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• pp.181-187
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• 1986

$trans-Cr^{Ⅲ}N_4XY$착물의 광화학적 치환반응에 있어서 한개의 리간드가 떨어져서 생기는 가상적 1차중간체의 총안정화에너지를 고려함으로서 치환되는 리간드를 예측할 수 있다. 총안정화 에너지와 d-궤도함수의 1전자에너지준위는 각종첩모형체계내에서 계산하였는데, 계산결과에 의하면 총안정화에너지 값이 큰 중간체일수록 보다 쉽게 생성된다고 할 수 있다. 결과적으로 총안정화에너지의 상대적인 값은 가장 낮은 에너지의 d-d전이에 해당하는 파장의 빛을 쪼여줄 때 $trans-Cr^{Ⅲ}N_4XY$착물에서 어느 리간드가 우선적으로 불안정하게 되는가를 결정하는데 이용될 수 있으며, $trans-Cr^{Ⅲ}N_4XY$착물의 광수화반응에 있어서 떨어지는 리간드에 대한 이러한 예측은 실험상의 결과와 일치하고 있다.

• Asian Journal of Atmospheric Environment
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• 제12권1호
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• pp.17-29
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• 2018

For the first time in the city of Riyadh, the formation of $O_3$ and its relationship with NO and $NO_2$ ($NO_x$) was investigated. Throughout the summer $O_3$, NO, and $NO_2$ were collected from three locations: residential, industrial, and rural areas. During the sampling period $O_3$ concentrations exceeded 1-hour local standards a few times yet remained consistent with the standards most of the time. The $O_3$ concentrations were observed highest in the rural location and lowest in the industrial area. The diurnal variation of NO followed a double peak: one in the morning and the other in the evening, representing the traffic pattern. Early morning NO peaks were observed in the rural location, which were attributed to the movement of NO from other locations. The $O_3$ concentrations depicted typical pattern, increasing after sunrise and reaching its maximum during midday. The highest $O_3$ concentrations were observed in the rural location followed by the residential and industrial. $NO_2$ photolysis rates were 3-4 times higher compared to other similar investigations, potentially due to intense solar radiation. A strong negative correlation was observed between $NO_x$ and $O_3$ values in the industrial location indicating photochemical activities around the industrial area were higher, likely due to additional $NO_x$ emissions from industries. Regression analysis of $NO_x$ and OX ($O_3+NO_2$) indicated that in residential and industrial locations at nighttime there were large $NO_x$ independent regional contributions which is attributed to VOCs. The Weekend Effect was observed in the city potentially due to the production of the OH radical and subsequent reactions with VOCs implying that the area is VOC-sensitive.