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以重庆某非规范填埋场为例,针对西南地区已封场非规范垃圾填埋场的稳定化进程进行了分析。按照场地布局选取4个采样点,在垃圾体上进行钻孔取样,分析不同深度的垃圾样pH值、有机质、含水率、生物可降解度以及垃圾样浸出液和填埋气组成以及各个指标随着填埋深度的变化规律,确定不同深度垃圾体的稳定化程度。结果表明,场内垃圾已呈现矿化垃圾特征;有机质、BDM、浸出液COD以及填埋气CH4含量等4个指标与填埋深度均较好地符合一级降解反应,可以预测垃圾体稳定化临界填埋深度。根据有机质、BDM、浸出液COD以及填埋气CH4含量等4个指标与填埋深度一级降解反应函数预测临界稳定化深度为15 m,与实测值判定的稳定化填埋深度相一致性。在对非规范垃圾填埋场场地利用过程中,需要先对未稳定的上层垃圾进行清理,并在已稳定的底层垃圾体上充填其他稳定介质后利用该地块。 相似文献
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建立了以EDTA和柠檬酸为铁盐络合剂的循环脱硫体系,采用络合铁法对垃圾填埋气中的H2S进行脱硫中试实验,结果表明实验所建立的络合铁脱硫体系运行稳定,脱硫效率高,适合应用于垃圾填埋气中硫化氢脱除。 相似文献
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我国城市中尚有大量非规范生活垃圾填埋场存在,对其进行污染整治消除填埋气导致的环境安全隐患刻不容缓.以重庆某垃圾填埋场为例,研究重庆市主城区的非规范生活垃圾填埋场填埋气的横向迁移问题,在垃圾场周边区域布设36个监测井,对监测井中的填埋气进行分析监测,以填埋气特征组分CH4气体的体积浓度变化研究填埋气的横向迁移规律.结果表明,监测井到填埋场边界的距离为监测井中CH4气体浓度的主要影响因素;垃圾场周边距离填埋场场界50 m以外的区域,填埋气的横向迁移已经相当微弱;但是距离填埋场边界50 m以内区域的填埋气的横向迁移明显,需要在距离填埋场边界50 m范围内采取措施与场内填埋气的导排措施配合,进行填埋气的污染控制. 相似文献
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循环流化床锅炉燃烧城市生活垃圾的研究进展 总被引:1,自引:0,他引:1
城市生活垃圾(MSW)产量的与日俱增及环保要求的不断提高,使循环流化床(CFB)燃烧技术逐渐在MSW的回收和利用方面扮演越来越重要的角色。简要分析了国内外采用分类回收及综合利用、卫生填埋、堆肥和一般焚烧方法处理MSW的不足之处以及采用CFB燃烧技术的优越性,重点介绍了国内外采用CFB燃烧装置焚烧MSW的研究和应用现状,指出了目前存在的问题及努力的方向。采用CFB燃烧装置焚烧MSW关于SO2、NOx、CO排放的实验研究和运行结果令人满意,但对HCl、二恶英及重金属排放还需要进一步研究。试验及实际运行结果都表明,采用CFB燃烧装置对MSW进行焚烧处理是切实可行的,它将是未来解决MSW问题的重要手段。 相似文献
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两种填埋结构中氨氮的空间变化规律研究 总被引:1,自引:0,他引:1
依据准好氧填埋和厌氧填埋的原理,构建了准好氧和厌氧填埋的实验室模拟装置,研究了2种填埋结构渗滤液中氨氮的空间分布规律。结果表明,准好氧填埋结构3层渗滤液中氨氮浓度都呈不断稳定下降的趋势,29周时上层、中层和下层渗滤液中氨氮浓度分别从填埋初的931.8、1796和3019 mg/L下降到25.6、328.9和820.1 mg/L;厌氧填埋结构3层渗滤液中氨氮浓度下降趋势不明显且波动性较大。准好氧填埋与厌氧填埋结构渗滤液中氨氮浓度表现出明显的空间层次效应,为下层>中层>上层。 相似文献
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H. A Belyea W. J Holland 《Journal of the Air & Waste Management Association (1995)》2013,63(5):320-323
Field tests were conducted on 82 fuel-burning installations ranging from 50 to 500 hp, fired with residual fuel oils. A flame pyrometer was used to measure peak flame temperatures. Coarse particulates were measured by impingement on adhesive paper strips inserted at right angles to the gas flow and fine particulates by filtration of the gas sample through filter paper. Both were evaluated using a standard Bacharach Scale. The tests clearly established that both coarse and fine particulate matter invariably occurred with low flame temperatures but decreased appreciably when peak flame temperatures reached approximately 2650°F; Minimum values were observed at temperatures somewhere between 2750 and 2850°F. This research was conducted as a result of the problem of acid smut and carbonaceous (ceno-sphere) fallout which appears to have increased with the advent of modern high-efficiency low-temperature heating installations and taller, cooler operating chimneys; sudden deluges of particles from the chimney serving large oil-burning plants soil clothing, pit car finishes, and damage nylon stockings and other materials. 相似文献
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Acrylonitrile-butadiene-styrene (ABS) copolymers without and with a polybrominated epoxy type flame retardant were thermally degraded at 450 degrees C alone (10 g) and mixed with polyvinylchloride (PVC) (8 g/2 g). Gaseous and liquid products of degradation were analysed by various gas chromatographic methods (GC with TCD, FID, AED, MSD) in order to determine the individual and cumulative effect of bromine and chlorine on the quality and quantity of degradation compounds. It was found that nitrogen, chlorine, bromine and oxygen are present as organic compounds in liquid products, their quantity depends on the pyrolysed polymer or polymer mixture. Bromophenol and dibromophenols were the main brominated compounds that come from the flame retardant. 1-Chloroethylbenzene was the main chlorine compound observed in liquid products. It was also determined that interactions appear at high temperatures during decomposition between the flame retardant, PVC and the ABS copolymer. 相似文献
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A multiresidue solid-phase extraction (SPE) method for the isolation and subsequent gas chromatographic determination of organochlorine and organophosphorus pesticide residues in low-moisture, nonfatty products is described. Residues are extracted from samples with an acetonitrile/water mixture. Cleanup of the extract is performed using graphitized carbon black and anion exchange SPE columns, and analysis is performed by gas chromatography with Hall electrolytic conductivity and flame photometric detection. Recovery data was obtained by fortifying corn, oats and wheat with pesticides. The average recoveries were 79-123% for eight organochlorine and 51-122% for 28 organophosphorus pesticide residues. The limit of quantitation for chlorpyriphos was 0.05 ppm using the Hall electrolytic conductivity detector and < 0.005 ppm using the flame photometric detector. 相似文献
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《Chemosphere》1986,15(4):461-470
Butyltin compounds in the 1–100 ng Sn/Liter range are solvent extracted from estuarine waters and derivatized with n-hexyl magnesium bromide. This forms tetraalkyltins that are quantified by gas chromatography with flame photometric detection and confirmed by gas chromatography mass spectrometry. The n-hexyl derivatives of methyltin and butyltin species are easily separated, and quantified relative to an internal standard, tripentyltin chloride. 相似文献
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Frank J. Schenck Vinetta Howard‐King 《Journal of environmental science and health. Part. B》2013,48(1):1-12
Abstract A multiresidue solid‐phase extraction (SPE) method for the isolation and subsequent gas Chromatographie determination of organochlorine and organophosphorus pesticide residues in low‐moisture, nonfatty products is described. Residues are extracted from samples with an acetonitrile/water mixture. Cleanup of the extract is performed using graphitized carbon black and anion exchange SPE columns, and analysis is performed by gas chromatography with Hall electrolytic conductivity and flame photometric detection. Recovery data was obtained by fortifying corn, oats and wheat with pesticides. The average recoveries were 79–123% for eight organochlorine and 51–122% for 28 organophosphorus pesticide residues. The limit of quantitation for chlorpyriphos was 0.05 ppm using the Hall electrolytic conductivity detector and <0.005 ppm using the flame photometric detector. 相似文献
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Donald F. Adams 《Journal of the Air & Waste Management Association (1995)》2013,63(9):963-968
This paper presents initial measurement data on the emission of volatile, reduced sulfur-containing gases from flue gas desulfurization (FGD) storage ponds. Several different types of FGD stored sludges were studied including lime, limestone, and mixtures of fly ash and lime or limestone residues, some of which had been chemically stabilized. The volatile sulfur gas emissions were cryogenically concentrated and determined by wall-coated, open-tubular capillary column gas chromatography using a flame photometric detector. Hydrogen sulfide, carbonyl sulfide, dimethyl sulfide, carbon disulfide, and an unusual, unidentified sulfur-containing compound were found in the gaseous pond flux. Benzene, toluene, and α-pinene were also identified by gas chromatography-single ion monitoring mass spectrometry. The total reduced sulfur gas emission from a 100 acre pond approximated 2.0 kg day?1 (as sulfur). 相似文献
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Combustion of brominated flame retardants and behavior of its byproducts 总被引:13,自引:0,他引:13
Sakai S Watanabe J Honda Y Takatsuki H Aoki I Futamatsu M Shiozaki K 《Chemosphere》2001,42(5-7):519-531
The substance flow rate of PBDDs/DFs into flue gas and incineration residues from incineration of three types of waste samples containing brominated flame retardants were examined. The samples used consisted of PBDEs (a typical retardant), used TV casing materials (actual waste materials), and waste printed circuit boards. PBDDs/DFs concentrations in the experimental samples of PBDEs/PE, waste TV casing materials and printed circuit boards ranged between 3000 and 130,000 ng/g. These values are very high when compared to other investigations. The increase of chlorine concentration in input sample reduced the ratio of PBDDs/DFs in flue gas and raised the ratio of PCDDs/DFs. With adequate combustion control and flue gas treatment, the amount of PBDDs/DFs released from the incineration of resin containing brominated flame retardants was lower than the input amount. The presence of PBDDs/DFs in incineration residues dominated the total amount of dioxins released. When PBDDs/DFs, PCDDs/DFs and PXDDs/DFs were considered as a total, the total amount released was lower than the total amount input. 相似文献
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Strosher MT 《Journal of the Air & Waste Management Association (1995)》2000,50(10):1723-1733
Emissions from flares typical of those found at oil-field battery sites in Alberta, Canada, were investigated to determine the degree to which the flared gases were burned and to characterize the products of combustion in the emissions. The study consisted of laboratory, pilot-scale, and field-scale investigations. Combustion of all hydrocarbon fuels in both laboratory and pilot-scale tests produced a complex variety of hydrocarbon products within the flame, primarily by pyrolytic reactions. Acetylene, ethylene, benzene, styrene, ethynyl benzene, and naphthalene were some of the major constituents produced by conversion of more than 10% of the methane within the flames. The majority of the hydrocarbons produced within the flames of pure gas fuels were effectively destroyed in the outer combustion zone, resulting in combustion efficiencies greater than 98% as measured in the emissions. The addition of liquid hydrocarbon fuels or condensates to pure gas streams had the largest effect on impairing the ability of the resulting flame to destroy the pyrolytically produced hydrocarbons, as well as the original hydrocarbon fuels directed to the flare. Crosswinds were also found to reduce the combustion efficiency (CE) of the co-flowing gas/condensate flames by causing more unburned fuel and the pyrolytically produced hydrocarbons to escape into the emissions. Flaring of solution gas at oil-field battery sites was found to burn with an efficiency of 62-82%, depending on either how much fuel was directed to flare or how much liquid hydrocarbon was in the knockout drum. Benzene, styrene, ethynyl benzene, ethynyl-methyl benzenes, toluene, xylenes, acenaphthalene, biphenyl, and fluorene were, in most cases, the most abundant compounds found in any of the emissions examined in the field flare testing. The emissions from sour solution gas flaring also contained reduced sulfur compounds and thiophenes. 相似文献
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Gas emissions of carbon dioxide, methane, dimethylsulfide, carbon monoxide and oxygen from a coal stockpile in Velenje were determined. Gases from the coal stockpile were collected in Alltech Standard sampling bags and then analysed using a capillary gas chromatograph and electrochemical sensors. A flame ionisation detector equipped with a Zr/Ni catalytic reactor was used for the determination of methane and carbon dioxide. Dimethylsulfide was detected with a flame photometric detector, and the concentrations of carbon monoxide and oxygen were determined by use of electrochemical sensors. The results showed that the main influence on gas emissions is related to the ambient temperature. Emissions of carbon dioxide during summer 2001 (average temperature during sampling period was 24 degrees C) were approximately 30-times higher than during winter 2002 (average temperature during sampling period was -2 degrees C) and were also influenced by the oxygen concentration. Carbon dioxide is mainly formed by oxidation of coal. Methane and dimethylsulfide are desorbed from coal, and are present in higher concentrations in stockpile emissions when stockpiles are renewed. The dimethylsulfide concentration, in contrast to laboratory experiments in stockpile emissions, falls immediately due to photo-degradation. 相似文献