Considering the characteristics of aldehydes among volatile organic compounds, a combined process was established by linking an absorbent and a photocatalytic reactor. Experiments to find the optimal operating conditions of the combined process showed that as the amount of photocatalyst coating increases, the wavelength of the ultraviolet lamp used becomes shorter, the photodegradation rate becomes faster, and the removal efficiency increases. It was also demonstrated that by controlling the relative humidity during the connection process of the combined process, the re-evaporation phenomenon at the front end (absorption area) of the hybrid process can be improved and the removal efficiency at the back end (photocatalytic reaction area) can be significantly enhanced. This confirmed the need for a combined process that complements the advantages and disadvantages of each process.

We used the measurement data derived from a proton transfer reaction time-offlight mass spectrometry (PTR-ToF-MS) to ascertain the source profile of volatile organic compounds (VOCs) from 4 major industrial classifications which showed the highest emissions from a total of 26 industrial classifications of A industrial complex. Methanol (MOH) was indicated as the highest VOC in the industrial classification of fabricated metal manufacture, and it was followed by dichloromethane (DM), ethanol (EN) and acetaldehyde (AAE). In the industrial classification of printing and recording media, the emission of ethylacetate (EA) and toluene (TOL) were the highest, and were followed by acetone (ACT), ethanol (EN) and acetic acid (AA). TOL, MOH, 2-butanol (MEK) and AAE were measured at high concentrations in the classification of rubber and plastic manufacture. In the classification of sewage, wastewater and manure treatment, TOL was the highest, and it was followed by MOH, H2S, and ethylbenzene (EBZ). In future studies, the source profiles for various industrial classifications which can provide scientific evidence must be completed, and then specified mitigation plans of VOCs for each industrial classification should be established.

The concentration of TVOCs in public transportation in the spring and summer of 2018 was measured. Public transportation measured the concentration of TVOCs on six subway lines in Seoul, two lines of high-speed trains, and intercity buses. The measurements were taken during the operation of each route of the surveyed public transportation from the origin to the destination. In addition, the measurement time was divided into the congestion time and the non-congestion time. In the spring of 2018, in the order of subway, train A, train B, and intercity buses, TVOC concentrations during the congestion time zone were 205.9 μg/m3, 121.3 μg/m3, 171.1 μg/m3, and 88.7 μg/m3, respectively. During the non-congestion time zone, the concentrations were 177.2 μg/m3, 108.8 μg/ m3, 118.2 μg/m3, and 126.1 μg/m3, respectively. In the summer of 2018, TVOC concentrations in the order of the aforementioned transportation modes during the congestion time zone were 169.8 μg/m3, 175.8 μg/m3, 78.0 μg/ m3, and 185.3 μg/m3, respectively. During the non-congestion time zone, the concentrations were 210.8 μg/m3, 116.1 μg/m3, and 162.7 μg/m3, respectively. An analysis of BTEX concentration among VOCs in public transportation in descending order were followed by toluene > xylene > ethylbenzene > benzene. Toluene, which has the highest concentration among the BTEX compounds, was found to be 12.86 μg/m3 to 91.41 μg/m3 during spring congestion time and 7.10 μg/m3 to 39.52 μg/m3 during non-congestion time. During the summer congestion time, the concentration was 6.68 μg/m3 to 249.48 μg/m3 and 13.23 μg/m3 to 214.5 μg/m3 during the non-congestion time. The concentration of benzene was mostly less than 5 μg/m3 in transportation. Particularly in the case of toluene, the concentration is significantly higher than that of other VOCs. Accordingly, further study of toluene exposure hazards will be needed. Five percent of the surveyed TVOC concentrations exceeded the recommended indoor air quality standard of 500 μg/m3, and all 13 cases representing this percentage were found in the subway. In addition, nine of the 13 cases that exceeded the recommended standard were measured during congestion time. Therefore, VOCs in public transportation vehicles during congestion time need to be managed.

Organic-inorganic hybrid perovskite nanocrystals have attracted a lot of attention owing to their excellent optical properties such as high absorption coefficient, high diffusion length, and photoluminescence quantum yield in optoelectronic applications. Despite the many advantages of optoelectronic materials, understanding on how these materials interact with their environments is still lacking. In this study, the fluorescence properties of methylammonium lead bromide (CH3NH3PbBr3, MAPbBr3) nanoparticles are investigated for the detection of volatile organic compounds (VOCs) and aliphatic amines (monoethylamine, diethylamine, and trimethylamine). In particular, colloidal MAPbBr3 nanoparticles demonstrate a high selectivity in response to diethylamine, in which a significant photoluminescence (PL) quenching (~ 100%) is observed at a concentration of 100 ppm. This selectivity to the aliphatic amines may originate from the relative size of the amine molecules that must be accommodated in the perovskite crystals structure with a narrow range of tolerance factor. Sensitive PL response of MAPbBr3 nanocrystals suggests a simple and effective strategy for colorimetric and fluorescence sensing of aliphatic amines in organic solution phase.

n-Nonane, 1¸2¸4-trimethylbenzene (124-TMB), toluene, total xylene (TXYL), isopropyl alcohol (IPA), and methyl ethyl alcohol (MEK) are major volatile organic compounds (VOCs) emitted from printing industries. The absorption amount of a single VOC per unit weight of silicone oil was as follows in the order of 189.5 g/kg-silicone oil for n-nonane, 91.7 g/kg-silicone oil for 124-TMB, and 60.1 g/kg-silicone oil for TXYL. Although hydrophobic VOCs were more absorbed in silicone oil than hydrophilic VOCs such as IPA and MEK, IPA and MEK, which had log Kow values of 1 or less, also were absorbed more than 26.0 g/kg-silicone oil. In two and three mixed VOCs of n-nonane, 124-TMB, and toluene, the absorption amount of each in silicon oil was less than that of single a VOC. The total absorption amount of two mixed VOCs ranged from 47.9 g to 138.7 g/kg-silicone oil, and the total absorption amount of three mixed VOCs was 65.8 g/kg-silicone oil. These results suggest that silicone oil is a promising pretreatment solution capable of absorbing high concentrations of VOCs that are intermittently emitted from printing industries. The absorption information of VOCs obtained in this study can be used as the design parameters of a damping device for the pretreatment of VOCs.

The concentrations of odor and volatile organic compound (VOC)-inducing substances were measured using selected ion flow tube mass spectrometers (SIFT-MS). SIFT-MS can continuously measure the concentration of odor-causing substances and VOCs in real time without pre-treatment steps. Measurements were conducted during the day and at night at 10 spots in the chemical block of the Sihwa industrial complex. Similar measurement results were observed in the daytime and nighttime for materials except methyl ethyl ketone with high concentrations. A high concentration of hydrogen sulfide was also measured at night. It is expected that an amount of emissions of VOCs and odor-causing substances under the absence of inspection can be traced if measured at other industrial complexes in vulnerable times.

The concentrations of volatile organic compounds (VOCs) and odor-inducing substances were measured using selected ion flow tube mass spectrometers (SIFT-MS) and a drone equipped with an air quality monitoring system. SIFT-MS can continuously measure the concentration of VOCs and odor-inducing substances in realtime without any pre-treating steps for the sample. The vehicle with SIFT-MS was used for real-time measurement of VOC concentration at the site boundaries of pollution sources. It is possible to directly analyze VOCs concentration generated at the outlets by capturing air from the pollution sources with a drone. VOCs concentrations of nine spots from Banwol National Industrial Complex were measured by a vehicle equipped with SIFT-MS and were compared with the background concentration measured inside the Metropolitan Air Quality Management Office. In three out of the nine spots, the concentration of toluene, xylene, hydrogen sulfide, and methyl ethyl ketone was shown to be much higher than the background concentration. The VOCs concentrations obtained using drones for high-concentration suspected areas showed similar tendencies as those measured using the vehicle with SIFTMS at the site boundary. We showed that if both the drone and real-time air quality monitoring equipment are used to measure VOCs concentration, it is possible to identify the pollutant sources at the industrial complex quickly and efficiently check sites with high concentrations of VOCs.

본 연구에서는 합성가스의 에너지화를 위한 가스엔진 성능 평가를 수행하였다. 회전수 1800 rpm 조건에서 공기과잉률이 1, 1.1, 1.2, 1.3, 1.4, 1.5, 1.6 증가에 따른 엔진출력(kWm)과 열효율(%)을 평가한 결과, 공기과잉률 λ 1.4에서 엔진출력 34 kWm를 나타냈으며, 공기과잉률이 증가할수록 엔진 열효율은 전반적으로 감소하는 경향을 보였다. 엔진출력 34 kWm 조건에서 공기과잉률이 1, 1.1, 1.2, 1.3, 1.4 증가시 열효율이 34.2%, 36.9%, 37.2%, 37.4%, 38.1%로 증가하였고, 발전출력을 통한 종합효율은 발전출 력 30 kWe 부하조건에서 38.7 kg/h의 연료를 소모하여 32.1%의 발전효율과 냉각수와 배기가스에서의 열 회수를 통해 57.3 kW의 폐열을 회수하여 53.8%의 열을 회수하여 총 85.8%의 종합효율을 보이는 것으로 나타났다.

In this study, we listed the VOCs focusing on ozone precursors emitted from printing shops in urban areas. The emission characteristics of the VOCs from workplaces were evaluated in terms of the used inks. As a result of field measurements, more than 80% of detected VOCs showed high values of photochemical ozone creation potential (POCP). The main species were aromatic hydrocarbons such as ethylbenzene, toluene, ethyltoluene, xylene, trimethylbenzene and their isomers, and paraffin hydrocarbons such as nonane, decane, and octane. Comparative examination between pristine ink and the printing process revealed the emission of hydrocarbons with 8 to 12 carbons such as o-xylene to n-dodecane from the used inks and with 3 to 7 carbons such as acetone to 3-methylhexane from the printing process. The major contributors to ozone production in printing industries were toluene (12.2%), heptane (7.43%), and 1,2,3-trimethylbenzene (7.21%) in every step.

본 연구는 스파티필름의 수분 스트레스 정도에 따라 실내 공간 내 오염물질 제거 효율을 구명하고자 수행하였다. 식물이 없는 공간을 대조구, 정상적인 스파티필름과 수분 스트레스를 받은 스파티필름을 각각의 처리구로 하였다. 스파티필름의 수분 스트레스 유무에 따른 chamber 내 온도를 조사한 결과 대조구와 처리구 모두 식물의 생육 적정 범위인 23±1℃를 유지하였으며, 처리 간의 0.7℃의 차이를 보였다. 습도의 경우 대조구와 처리구는 유의차 있게 나타났으며, 처리 간의 유의 차는 없는 것으로 나타났다. 수분 스트레스에 따른 실내 오염 물질을 조사한 결과, 포름알데히드(Formaldehyde) 경우 대조구는 0.30mg･m-3, 정상적인 스파티필름은 0.05mg･m-3 , 수분 스트레스를 받은 스파티필름은 0.09mg･m-3으로 대조구와 처리구는 통계적으로 유의차를 보였으며, 식물 내 수분 스트레스에 따른 처리구간에는 유의차가 없었다. TVOC(Total Volatile Organic Compound)조사 결과, 정상적인 스파티필름의 TVOC는 5시간 후 0.00mg･m-3 으로 모두 제거 된 반면, 수분 스트레스를 받은 스파티필름은 0.34mg･m-3으로 다소 남아 있었으며, 대조구는 1.25mg･m-3으로 세 처리 모두 통계적으로 유의차 있게 나타났다. 또한 이산화탄소 변화량 조사결과, 대조구는 459ppm, 정상 스파티필름은 446ppm으로 통계적으로 유의한 차이는 없으며, 수분 스트레스를 받은 스파티 필름이 대조구보다 이산화탄소 함량이 다소 높았다. 기공변화율 조사 결과, 정상 스파티필름의 변화율은 높게 나타났으며, 수분 스트레스를 받은 스파티필름은 변화율이 낮은 것으로 조사되었다. 따라서, 스파티필름이 배치되어있지 않은 공간보다 배치된 공간이 공기정화에 효과적이며, 수분 스트레스를 받은 스파티필름은 실내오염물질 제거에 있어서 기공 변화율 및 이산화탄소 흡수능력이 저하되므로 스파티필름을 이용하여 효과적으로 실내오염물질을 제거하기 위해서는 적절한 수분 관리가 필요한 것으로 판단된다.

In this study, we measured the concentration of total volatile organic compounds (TVOCs) in four different seasons from 2016 to 2017 in order to determine seasonal variation of indoor air quality in relation to public transportation modes (subways, trains, and express buses). The measurement was carried out both during rush hour when traffic was congested as well as during non-rush hour when traffic was not congested. Effects by season, degree of congestion, and characteristics of public transportation were analyzed on the basis of 295 items of data during the periods of congestion and 295 items of data during the periods of non-congestion. The average TVOCs concentration in winter was the highest with 226.4 μg/m 3 . The average TVOCs concentration on an express bus was the highest with a seasonal average of 142.3 μg/m 3 . The TVOCs concentration in the period of congested traffic was higher than in the period of non-congested traffic for all public transportation modes. For the average TVOCs concentration by season and transportation, there was no data that exceeded the guidelines regarding maintaining indoor air quality. However, 2.5% of all sample measured data (TVOCs) exceeded the guidelines regarding maintaining indoor air quality. Therefore, the continuous monitoring of public transport vehicles is required.

This study was conducted to determine the absorption properties of silicone oil, liquid paraffin, and silicone rubber as absorbents for hydrophobic volatile organic compounds (VOCs) mainly emitted from the printing and publishing industry through VOCs absorption efficiency and partition coefficient. Also, changes in absorbability were tested through blending of absorbents and load of target VOCs mixtures. The results obtained can be used as fundamental data to choose an appropriate absorbent. All of the three absorbents showed an excellent absorption efficiency of above 98% for each 5 wt% load of the target VOCs including toluene, xylene, methyl ethyl ketone (MEK), isopropyl alcohol (IPA), 1,2,4-trimethylbenzene (124-TMB), and n-Nonane. In terms of toluene load, all absorbents showed good absorption efficiency of above 95% to a high load of 15 wt%. The air-absorbent partition coefficient of each target compound (P value) exhibited the highest value of 9.8 × 10−5 for 124-TMB in silicone rubber and the lowest value of 1.6 × 10−2 for IPA in liquid paraffin. These results indicate that the target VOCs had high affinity for the three absorbents. Absorption efficiency for the target VOCs at various absorbent blending ratios using three kinds of absorbents was improved to 99.9% regardless of the absorbent type or blending ratio. This result suggests that the shortcomings of single absorbents can be overcome through absorbent blending, enabling cost reduction and applicability to a dry-type treatment process. In treatment for mixture of the target VOCs to mimic an actual VOCs treatment, the absorption performances of silicone oil showed an absorption efficiency of 99% for 16 wt% of total VOCs load. These results indicated that silicone oil could be considered as a good absorbent.

A pilot-scale biocover was installed at a sanitary landfill for municipal waste, and the removal of volatile organic compounds (VOCs) by the biocover was evaluated for a long period of 550 days. The biocover (2.5 m W × 5 m L × 1 m H) was constructed with the mixture of soil, perlite, earthworm cast and compost (6:2:1:1, v/v). The total VOCs concentration of the inlet gas into the biocover was 820.3 ppb~7,217.9 ppb, and the total VOCs concentration of the outlet gas from the surface of the biocover was 12.6 ppb~1,270.1 ppb. The average removal efficiency of total VOCs was 87.6 ± 11.0% (60.5% for minimum and 98.5% for maximum). Toluene concentration was the highest among the inlet VOCs, followed by ethylbenzene, m, p-xylene and o-xylene. These aromatic VOCs accounted for more than 50% of the total VOCs concentration. Other than these aromatic VOCs, hexane, cyclohexane, heptane, benzene, and acetone were major VOCs among the inlet VOCs. Compared with the VOC profiles in the inlet gas, the relative contribution of dichloromethane to the outlet VOCs emitted from the biocover layer increased from 0.1% to 15.3%. The average removal efficiencies of BTEX in the biocover were over 84% during the operation period of 550 days. The average removal efficiencies of hexane, cyclohexane and heptane in the biocover were 86.0 ± 18.9%, 85.4 ± 20.4% and 97.1 ± 4.0%, respectively. The removal efficiency of VOCs in the biocover decreased not only when the ambient temperature had fallen below 5oC, but also when the ambient temperature had risen above 23oC. Information on the VOCs removal characteristics of the biocover installed in the landfill field can be useful for commercializing the biocover technology for the treatment of VOCs.

Volatile organic compounds(VOCs) are toxic carcinogenic compounds found in wastewater. VOCs require rapid removal because they are easily volatilized during wastewater treatment. Electrochemical advanced oxidation processes(EAOPs) are considered efficient for VOC removal, based on their fast and versatile anodic electrochemical oxidation of pollutants. Many studies have reported the efficiency of removal of various types of pollutants using different anodes, but few studies have examined volatilization of VOCs during EAOPs. This study examined the removal efficiency for VOCs (chloroform, benzene, trichloroethylene and toluene) by oxidization and volatilization under a static stirred, aerated condition and an EAOP to compare the volatility of each compound. The removal efficiency of the optimum anode was determined by comparing the smallest volatilization ratio and the largest oxidization ratio for four different dimensionally stable anodes(DSA): Pt/Ti, IrO2/Ti, IrO2/Ti, and IrO2-Ru-Pd/Ti. EAOP was operated under same current density (25 mA/cm2) and electrolyte concentration (0.05 M, as NaCl). The high volatility of the VOCs resulted in removal of more than 90% within 30 min under aerated conditions. For EAOP, the IrO2-Ru/Ti anode exhibited the highest VOC removal efficiency, at over 98% in 1 h, and the lowest VOC volatilization (less than 5%). Chloroform was the most recalcitrant VOC due to its high volatility and chemical stability, but it was oxidized 99.2% by IrO2-Ru/Ti, 90.2% by IrO2-Ru-Pd/Ti, 78% by IrO2/Ti, and 75.4% by Pt/Ti anodes The oxidation and volatilization ratios of the VOCs indicate that the IrO2-Ru/Ti anode has superior electrochemical properties for VOC treatment due to its rapid oxidation process and its prevention of bubbling and volatilization of VOCs.

Indoor Volatile organic compounds (VOCs) are classified as known or possible toxicants and odorants. This study characterized VOC levels in 11 homes in an area in the capital of Seoul by using two different methods of VOCs sampling, which are the active sampling using a thermal sorption tube and the passive sampling using a diffusion sampler. When using the active sampling method, the total target VOC concentration ranged from 41.7 to 420.7 μg/ m3 (mean 230.4 μg/m3; median 221.8 μg/m3) during winter and 21.3 to 1,431.9 μg/m3 (mean 340.1 μg/m3; median 175.4 μg/m3) during summer. When using the passive method, 29.6 to 257.5 μg/m3 (mean 81.8 μg/m3; median 49.4 μg/m3) during winter and 1.2 to 5,131.1 μg/m3 (mean 1,758.8 μg/m3; median 1,375.1 μg/m3) during summer. Forty-nine VOCs were quantified and toluene showed the highest concentration regardless of the season and the sampling method studied. The distribution of VOCs was relatively varied by using the active method. However, it showed a low correlation with indoor environmental factors such as room temperature, humidity and ventilation time. The correlation between indoor environmental factors and VOCs were relatively high in the passive method. In particular, these characteristics were confirmed by principal component analysis.

Two sewage treatment facilities were selected to identify odor emission characteristics, focusing on volatile organic compounds (VOCs) and sulfur compounds. The complex odor, 5 kinds of sulfur compounds and 23 kinds of VOCs were analyzed from gas and sludge storages. Hydrogen sulfide was detected in the highest concentration and had the highest odor quotient among the odorous compounds monitored in this study, demonstrating that the contribution of hydrogen sulfide to the complex odor reached up to 90%. For VOCs, the overall contribution to the complex odor was not critical but VOCs can sufficiently trigger an odorous sensation because the sum of the odor quotient reached up to 2.89.

This paper is a review on the treatment of volatile organic compounds using absorbents. Volatile organic compounds (VOCs) are carbon-based compounds with a boiling point ranging from 50℃ to 250℃. VOCs have been considered as contributors of photochemical smog and global warming as well as hazards to human health. VOCs can be removed by a variety of methods, including those that are destructive (incineration, catalytic oxidation, and biodegradation) and non-destructive (adsorption, absorption, and condensation). The removal performance of VOCs in the gas phase is influenced by gas-liquid mass transfer and/or the microbial activity depending on VOC properties such as solubility, diffusivity, bioavailability, and toxicity. Since the usual processes for VOCs removal involve water as a VOC absorbent, it is necessary to improve the removal efficiency of hydrophobic VOCs. In addition, VOC removal processes do not appear to show consistently satisfactory performance due to transient high-strength VOC loading in practical fields. To increase the gas-liquid mass transfer of hydrophobic VOCs and to prevent the functional deterioration due to transient high loading, the use of nonaqueous phase VOC absorbents is a promising strategy. This review offers a critical overview of the types, properties, and the applications of the VOC absorbents, including liquid organic solvents, ionic liquids, and solid polymers. This paper also details the advantages by employing the VOC absorbents for the removal of hydrophobic VOCs in the integrated process, absorption and biodegradation coupling process. The challenges of and future perspectives on the development of efficient VOC removal processes using VOC absorbents are briefly discussed.