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排序方式: 共有64条查询结果,搜索用时 31 毫秒
1.
Kuan Lun Pan Sheng Jen Yu Shaw Yi Yan 《Journal of the Air & Waste Management Association (1995)》2014,64(11):1260-1269
Direct decomposition of N2O by perovskite-structure catalysts including La2NiO4, LaSrNiO4, and La0.7Ce0.3SrNiO4 was investigated. The catalysts were prepared by the Pechini method and characterized by x-ray diffraction (XRD), BET, scanning electron microscopy (SEM), and O2-TPD. Experimental results indicate that the properties of La2NiO4 are significantly improved by partially substituting La with Sr and Ce. N2O decomposition efficiencies achieved with LaSrNiO4 and La0.7Ce0.3SrNiO4 are 44 and 36%, respectively, at 400ºC. As the temperature was increased to 600ºC, N2O decomposition efficiency achieved with LaSrNiO4 and La0.7Ce0.3SrNiO4 reached 100% at an inlet N2O concentration of 1,000 ppm, while the space velocity was fixed at 8,000 hr?1. In addition, effects of various parameters including oxygen, water vapor, and space velocity were also explored. The results indicate that N2O decomposition efficiencies achieved with LaSrNiO4 and La0.7Ce0.3SrNiO4 are not significantly affected as space velocity is increased from 8,000 to 20,000 hr?1, while La0.7Ce0.3SrNiO4 shows better tolerance for O2 and H2O(g). On the other hand, N2 yield with LaSrNiO4 as catalyst can be significantly improved by doping Ce. At a gas hour space velocity of 8,000 hr?1, and a temperature of 600ºC, high N2O decomposition efficiency and N2 yield were maintained throughout the durability test of 60 hr, indicating the long-term stability of La0.7Ce0.3SrNiO4 for N2O decomposition.
Implications:Nitrous oxide (N2O) not only has a high global warming potential (GWP100 = 310), but also potentially destroys ozone in the stratosphere. Pervoskite-type catalysts including La2NiO4, LaSrNiO4, and La0.7Ce0.3SrNiO4 are applied for direct N2O decomposition. The results show that N2O decomposition can be enhanced as Sr and Ce are doped into La2NiO4. At 600ºC, N2O decomposition efficiencies achieved with LaSrNiO4 and La0.7Ce0.3SrNiO4 reach 100%, demonstrating high activity and good potential for direct N2O decomposition. Effects of O2 and H2O(g) contents on catalytic activities are also evaluated and discussed. 相似文献
2.
Yi-Hsiu Jen Wei-Hsiang Chen Chung-Shin Yuan Iau-Ren Ie Chung-Hsuang Hung 《Environmental science and pollution research international》2014,21(8):5474-5483
This study investigated the tempospatial variation of atmospheric mercury and its gas-particulate partition in the vicinity of a semiconductor manufacturing complex, where a plenty of flat-monitor manufacturing plants using elemental mercury as a light-initiating medium to produce backlight fluorescence tubes and may fugitively emit mercury-containing air pollutants to the atmosphere. Atmospheric mercury speciation, concentration, and the partition of total gaseous mercury (TGM) and particulate mercury (Hgp) were measured at four sites surrounding the semiconductor manufacturing intensive district/complex. One-year field measurement showed that the seasonal averaged concentrations of TGM and Hgp were in the range of 3.30–6.89 and 0.06–0.14 ng/m3, respectively, whereas the highest 24-h TGM and Hgp concentrations were 10.33 and 0.26 ng/m3, respectively. Atmospheric mercury apportioned as 92.59–99.01 % TGM and 0.99–7.41 % Hgp. As a whole, the highest and lowest concentrations of TGM were observed in the winter and summer sampling periods, respectively, whereas the concentration of Hgp did not vary much seasonally. The highest TGM concentrations were always observed at the downwind sites, indicating that the semiconductor manufacturing complex was a hot spot of mercury emission source, which caused severe atmospheric mercury contamination over the investigation region. 相似文献
3.
Myrto Petreas Kai-Shen Liu Bei-Hung Chang Steven B. Hayward Ken Sexton 《Journal of the Air & Waste Management Association (1995)》2013,63(5):647-651
As part of the California Mobile Home Study, over 250 mobile homes from throughout the state were monitored for nitrogen dioxide (NO2) concentrations. Week-long average measurements were taken with Palmes tubes in the kitchen and bedroom of each mobile home during the summer of 1984 and the winter of 1985. The study was conducted entirely by mail with the participants providing all the necessary information. Mobile homes using gas for cooking had significantly higher indoor NO2 levels than those using electricity. Mobile homes located in the Los Angeles basin had significantly higher indoor NO2 concentrations than did mobile homes in the rest of the state. Gas cooking, the inverse of the house volume and geographic location (as a surrogate of outdoor NO2) were the most important variables identified by multiple linear regression. 相似文献
4.
Yuan CS Wang G Xue SH Ie IR Jen YH Tsai HH Chen WJ 《Journal of the Air & Waste Management Association (1995)》2012,62(7):799-809
A number of activated carbons derived from waste tires were further impregnated by gaseous elemental sulfur at temperatures of 400 and 650 degrees C, with a carbon and sulfur mass ratio of 1:3. The capabilities of sulfur diffusing into the micropores of the activated carbons were significantly different between 400 and 650 degrees C, resulting in obvious dissimilarities in the sulfur content of the activated carbons. The sulfur-impregnated activated carbons were examined for the adsorptive capacity of gas-phase mercuric chloride (HgC1) by thermogravimetric analysis (TGA). The analytical precision of TGA was up to 10(-6) g at the inlet HgCl2 concentrations of 100, 300, and 500 microg/m3, for an adsorption time of 3 hr and an adsorption temperature of 150 degrees C, simulating the flue gas emitted from municipal solid waste (MSW) incinerators. Experimental results showed that sulfur modification can slightly reduce the specific surface area of activated carbons. High-surface-area activated carbons after sulfur modification had abundant mesopores and micropores, whereas low-surface-area activated carbons had abundant macropores and mesopores. Sulfur molecules were evenly distributed on the surface of the inner pores after sulfur modification, and the sulfur content of the activated carbons increased from 2-2.5% to 5-11%. After sulfur modification, the adsorptive capacity of HgCl2 for high-surface-area sulfurized activated carbons reached 1.557 mg/g (22 times higher than the virgin activated carbons). The injection of activated carbons was followed by fabric filtration, which is commonly used to remove HgCl2 from MSW incinerators. The residence time of activated carbons collected in the fabric filter is commonly about 1 hr, but the time required to achieve equilibrium is less than 10 min. Consequently, it is worthwhile to compare the adsorption rates of HgCl2 in the time intervals of < 10 and 10-60 min. 相似文献
5.
K S Liu S B Hayward J R Girman B A Moed F Y Huang 《Journal of the Air & Waste Management Association》1991,41(9):1207-1212
A study was conducted to determine the annual average radon concentrations in California residences, to determine the approximate fraction of the California population regularly exposed to radon concentrations of 4 pCi/l or greater, and to the extent possible, to identify regions of differing risk for high radon concentrations within the state. Annual average indoor radon concentrations were measured with passive (alpha track) samplers sent by mail and deployed by home occupants, who also completed questionnaires on building and occupant characteristics. For the 310 residences surveyed, concentrations ranged from 0.10 to 16 pCi/l, with a geometric mean of whole-house (bedroom and living room) average concentrations of 0.85 pCi/l and a geometric standard deviation of 1.91. A total of 88,000 California residences (0.8 percent) were estimated to have radon concentrations exceeding 4 pCi/l. When the state was divided into six zones based on geology, significant differences in geometric mean radon concentrations were found between several of the zones. Zones with high geometric means were the Sierra Nevada mountains, the valleys east of the Sierra Nevada, the central valley (especially the southern portion), and Ventura and Santa Barbara Counties. Zones with low geometric means included most coastal counties and the portion of the state from Los Angeles and San Bernardino Counties south. 相似文献
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7.
T. L. Hayward 《Marine Biology》1980,58(4):295-309
Spatial and temporal feeding patterns (determined from an index of gut fullness) are described for 10 typical species of calanoid copepods collected from the North Pacific central gyre (September 1968 to June 1977), an area where the zooplankton is food limited and there were a-priori reasons to suspect that feeding and competition for food were important in regulating zooplankton community structure. Over 100 samples from 11 cruises to the eastern part of the gyre were examined, and patterns of gut fullness were related to environmental variables and the copepod species structure. The copepods studied all tended to be omnivores and food generalists. Males had lower indices of gut fullness than females but both males and females of a species had similar spatial and temporal feeding patterns. Guts were usually fuller at night than during the day, even in nonmigrating species; however, within nighttime depth distributions, no depths were preferred for feeding. There were also differences between species in mean gut fullness, but different species tended to have similar spatial and temporal feeding patterns. There was considerable spatial variability, and locales could be identified in which most species had higher indices of gut fullness. The copepods were not necessarily more abundant in these locales, nor did these tend to be areas of above average chlorophyll concentration. These patterns were consistent with relatively nonselective feeding, and there was no evidence that these species separate their niches by feeding at differing places or times. 相似文献
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9.
In situ chemical oxidation (ISCO) typically delivers oxidant solutions into the subsurface for contaminant destruction. Contaminants available to the oxidants, however, are limited by the mass transfer of hydrophobic contaminants into the aqueous phase. ISCO treatments therefore often leave sites with temporarily clean groundwater which is subject to contaminant rebound when sorbed and free phase contaminants leach back into the aqueous phase. Surfactant Enhanced In situ Chemical Oxidation (S‐ISCO®) uses a combined oxidant‐surfactant solution to provide optimized contaminant delivery to the oxidants for destruction via desorption and emulsification of the contaminants by the surfactants. This article provides an overview of S‐ISCO technology, followed by an implementation case study at a coal tar contaminated site in Queens, New York. Included are data points from the site which demonstrate how S‐ISCO delivers desorbed contaminants without uncontrolled contaminant mobilization, as desorbed and emulsified contaminants are immediately available to the simultaneously injected oxidant for reaction. ©2016 Wiley Periodicals, Inc. 相似文献
10.