垃圾填埋气火焰稳定特性试验研究

针对大气式燃烧器在燃烧垃圾填埋气时的火焰稳定特性进行了实验研究，设计了一种结构简单、效果明显的填埋气火焰稳定装置。这种装置对于低热值燃气的稳定燃烧能起到较好的作用。     

络合铁法脱除垃圾填埋气中的H_2S

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.     

非规范生活垃圾填埋场填埋气横向迁移规律及控制

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.     

络合铁法脱除垃圾填埋气中的H2S

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。     

循环流化床锅炉燃烧城市生活垃圾的研究进展

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.     

西南地区某已封场非规范垃圾填埋场垃圾稳定化进程分析

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。     

络合铁法脱除垃圾填埋气中的H2S

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。     

模拟成藏地质填埋及诱导填埋有机质生气的理论初探

填埋处理和垃圾生物气的开发利用是实现城市生活垃圾资源化、无害化、减量化处理的有效途径,引入模拟生物气成藏和含气系统的思路,开展地质填埋与诱导填埋有机质生气研究是对能源地质学和填埋设计理念的新探索.通过对比研究地质填埋结构与地质学中生物气藏系统的异同点、生气机理和影响因素的共性与差异,初步论证了将模拟生物气藏理论引入地质填埋设计、优化地质填埋结构、提高填埋有机质生物气化效率和抽排利用效率的可行性;探讨了生物气藏理论在构建地质填埋结构中的可能应用和启示.研究表明:模拟生物气藏地质填埋设计和非常规生物气开发理念具有理论依据和现实基础;生物气藏生、储、盖要素和运、圈、保过程的模拟可应用于垃圾地质填埋场的构建,微生物地球化学理论有助于对诱导填埋有机质生气条件优化的认识.     

垃圾填埋场填埋气产生与迁移计算机模拟

准确预测填埋场内填埋气随时间和空间的变化规律,对填埋场的管理和填埋气的合理应用具有重要作用.以多孔介质流体动力学理论为基础,构建了填埋场中气体迁移转化过程三维模型.应用有限单元法和迭代法对模型的非线性方程组进行了求解,计算了填埋场中气体的压力分布情况.结果表明,填埋初期气压随深度和时间的增加而增加;而后气压随时间增加逐渐减小.     

生活垃圾填埋场不同填埋方式填埋气特性研究

对于国内外在传统的厌氧填埋和新型的准好氧填埋两种不同运行方式下对填埋气的特性研究作了简介。通过比较分析，传统的厌氧填埋结构中填埋气的甲烷含量比较高（40％～60％），而准好氧填埋中填埋气的甲烷含量只有10％～20％。对于中小型的填埋场，由于技术和成本的制约，建立准好氧填埋场，不仅有利于加快垃圾的稳定化进程，还可以减少甲烷的生成量，减轻对环境所造成的污染。     

Flame Temperature in Oil-Fired Fuel-Burning Equipment and its Relationship to Carbonaceous Particulate Emissions

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.     

The individual and cumulative effect of brominated flame retardant and polyvinylchloride (PVC) on thermal degradation of acrylonitrile-butadiene-styrene (ABS) copolymer

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.     

Determination of organochlorine and organophosphorus pesticide residues in low moisture, nonfatty products using a solid phase extraction cleanup and gas chromatography

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.     

Determination of organochlorine and organophosphorus pesticide residues in low moisture,nonfatty products using a solid phase extraction cleanup and gas chromatography

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.     

Sulfur Gas Emissions from Flue Gas Desulfurization Sludge Ponds

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).     

Combustion of brominated flame retardants and behavior of its byproducts

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.     

Evaluation of gas emissions from coal stockpile

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.     

Characterization of emissions from diffusion flare systems

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.     

The Detection and Estimation of Part Per Billion Concentrations of Hydrocarbons

The addition of a freeze-out step in liquid nitrogen prior to analysis by gas chromatography with flame ionization detection permits the accurate determination of C₂ and higher hydrocarbons in the part per billion (ppb) range. Concentrations of C₂ and higher hydrocarbons have been measured in commercial cylinders of nitrogen, helium and hydrogen. Using a 150 ml sample of gas, recovery of ppb concentrations is 95 to 100 percent.