A dynamic dilution system was used for the study of the influence of ozone on the sampling and storage of volatile organic
compounds (VOCs) at 0, 4, 7 and 14 days in “TO-Can” canisters at two ozone concentrations, 60 and 150 ppbv. Among the 31 ozone
precursors VOCs, a representative mixture containing five alkenes, five aromatics, acetylene and 1,3 butadiene was selected
using the Clausius–Clapeyron equation. Here, we demonstrate that the presence of ozone have no influence on the concentrations
of VOCs after 14 days storage period and consequently no problem of representativity of the sampling appears after 14 days
of storage. The main explanation is the degradation of ozone in contact with deactivated walls of canisters. 相似文献
Volatile organic compounds (VOCs) and carbonyl compounds were measured both indoors and outdoors in 50 residences of Beijing in heating (December, 2011) and non-heating seasons (April/May, 2012). SUMMA canisters for VOCs and diffusive samplers for carbonyl compounds were deployed for 24 h at each site, and 94 compounds were quantified. Formaldehyde, acetone and acetaldehyde were the most abundant carbonyl compounds both indoors and outdoors with indoor median concentrations being 32.1, 21.7 and 15.3 μg·m−3, respectively. Ethane (17.6 μg·m−3), toluene (14.4 μg·m−3), propane (11.2 μg·m−3), ethene (8.40 μg·m−3), n-butane (6.87 μg·m−3), and benzene (5.95 μg·m−3) showed the high median concentrations in indoor air. Dichloromethane, p-dichlorobenzene (p-DCB) and toluene exhibited extremely high levels in some residences, which were related with a number of indoor emission sources. Moreover, isoprene, p-dichlorobenzene and carbonyls showed median indoor/outdoor (I/O) ratios larger than 3, indicating their indoor sources were prevailing. Chlorinated compounds like CFCs were mainly from outdoor sources for their I/O ratios being less than 1. In addition, indoor concentrations between two sampling seasons varied with different compounds. Carbonyl compounds and some chlorinated compounds had higher concentrations in the non-heating season, while alkanes, alkenes, aromatic compounds showed an increase in the heating season. Indoor concentration of VOCs and carbonyls were influenced by locations, interior decorations and indoor activities, however the specific sources for indoor VOCs and carbonyls could not be easily identified. The findings obtained in this study would significantly enhance our understandings on the prevalent and abundant species of VOCs as well as their concentrations and sources in Beijing residences. 相似文献
In this study, post plasma-catalysis degradation of mixed volatile organic compounds (benzene, toluene, and xylene) has been performed in a hybrid surface/packed-bed discharge plasma reactor with Ag-Ce/g-Al2O3 catalyst at room temperature. The effect of relative air humidity on mixed VOCs degradation has also been investigated in both plasma-only and PPC systems. In comparison to the plasma-only system, a significant improvement can be observed in the degradation performance of mixed VOCs in PPC system with Ag-Ce/γ-Al2O3 catalyst. In PPC system, 68% benzene, 89% toluene, and 94% xylene were degraded at 800 J·L–1, respectively, which were 25%, 11%, and 9% higher than those in plasma-only system. This result can be attributed to the high catalytic activity of Ag-Ce/γ-Al2O3 catalyst to effectively decompose O3 and lead to generating more reactive species which are capable of destructing the VOCs molecules completely. Moreover, the presence of Ag-Ce/γ-Al2O3 catalyst in plasma significantly decreased the emission of discharge byproducts (NOx and O3) and promoted the mineralization of mixed VOCs towards CO2. Adding a small amount of water vapor into PPC system enhanced the degradation efficiencies of mixed VOCs, however, further increasing water vapor had a negative impact on the degradation efficiencies, which was primarily attributed to the quenching of energetic electrons by water vapor in plasma and the competitive adsorption of water vapor on the catalyst surface. Meanwhile, the catalysts before and after discharge were characterized by the Brunauer-Emment-Teller and X-ray photoelectron spectroscopy.
Concentrations of volatile organic compounds (VOCs) of the city air in Oba Akran road, Lagos were investigated. The chlorinated VOCs and xylene in Oba Akran were high. The average benzene/toluene ratio in Oba Akran was 1.7 suggesting that vehicular emission was a possible VOC source in most areas of Oba Akran. The toluene/(m+p-xylene) ratio also suggests a common source of toluene and xylene at these sites, presumably organic solvent used by industries located at Oba Akran. Our results showed that 7.10 tons of CO 2 equivalents of VOCs are being emitted per year from Oba Akran. Xylenes were found to be the largest contributor to the ozone formation followed by trichloroethylene. A multivariate statistical analysis (Factor analysis extracted with Principal Component Analysis) has been applied to a set of data, and it was found that the main principal components, extracted from the air VOC pollution data, were related to gasoline and oil combustion/industrial activities. 相似文献
• Applications of non-thermal plasma reactors for reduction of VOCs were reviewed.• Dielectric barrier discharge (DBD) plasma was considered.• Effect of process parameters was studied.• Effect of catalysts and inhibitors were evaluated. Volatile organic compounds (VOCs) released from the waste treatment facilities have become a significant issue because they are not only causing odor nuisance but may also hazard to human health. Non-thermal plasma (NTP) technologies are newly developed methods and became a research trend in recent years regarding the removal of VOCs from the air environment. Due to its unique characteristics, such as bulk homogenized volume, plasma with high reaction efficiency dielectric barrier discharge (DBD) technology is considered one of the most promising techniques of NTP. This paper reviews recent progress of DBD plasma technology for abatement of VOCs. The principle of plasma generation in DBD and its configurations (electrode, discharge gap, dielectric barrier material, etc.) are discussed in details. Based on previously published literature, attention has been paid on the effect of DBD configuration on the removal of VOCs. The removal efficiency of VOCs in DBD reactors is presented too, considering various process parameters such as initial concentration, gas feeding rate, oxygen content and input power. Moreover, using DBD technology, the role of catalysis and inhibitors in VOCs removal are discussed. Finally, a modified configuration of the DBD reactor, i.e. double dielectric barrier discharge (DDBD) for the abatement of VOCs is discussed in details. It was suggested that the DDBD plasma reactor could be used for higher conversion efficiency as well as for avoiding solid residue deposition on the electrode. These depositions can interfere with the performance of the reactor. 相似文献
Urban energy consumption is one of the most important causes of air pollution. Air pollution-oriented ecological risk assessment is of great significance to the promotion of urban environmental protection. This paper focuses on ecological risk in Xiamen city caused by air pollutant discharge from urban energy consumption. The Long-range Energy Alternatives Planning model was used to establish two scenarios of energy consumption in Xiamen city, and based on different scenarios, we estimated urban energy consumption and discharge quantity of air pollutant (DQAP). A box model and an expert scoring method were used to calculate the air pollution burden (APB) of SO2, NO2, CO, PM10 and PM2.5 and to obtain the probabilities of different air pollution loads. An ecological risk assessment model was developed and utilized to predict Xiamen city’s ecological risks in 2020. The results showed that under an energy-saving scenario, the ecological risks for PM2.5, SO2 and NO2 are high, whereas the ecological risks for CO and PM10 are low. Under a baseline scenario, the ecological risks for PM2.5, SO2 and NO2 are moderate, whereas the ecological risks for CO and PM10 are low. In addition, the APB of SO2, NO2, CO, and PM2.5, but not of PM10, is predicted to rise. In the simulation, energy generation from coal is the main source of air pollution. Although the DQAP from automobiles is not high, it is predicted to rise year-on-year. In summary, the ecological risk due to pollution in Xiamen city is high, and the main pollutants are SO2, NO2 and PM2.5. 相似文献
A practical method for the quantification of total purgeable organic sulfur (POS) in highly contaminated groundwater is described.
Volatile organic sulfur compounds (VOSC) are purged from the water samples by a stream of oxygen and combusted. The emerging
sulfur dioxide is absorbed in H2O2 and converted to sulfate which is quantified by ion chromatography and reported as mass sulfur equivalent. The overall limit
of quantification is 0.03 mg l−1. The content of POS is balanced with the total VOSC determined by GC-AED after liquid–liquid extraction. Separate determination
of the non-volatile organic sulfur compounds by direct combustion of the water sample and adsorption to charcoal yielded a
mass balance of the total sulfur content. Semi-quantitative GC-MS after purge & trap accumulation revealed that the VOSC mixture
is composed of C1–C4 alkyl sulfides. The implementation of the developed methodology for the quantification of VOSC as potential catalyst poison
in a cleaning plant for groundwater contaminated with volatile haloorganics (VOX) is presented. 相似文献
