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.     

固体回收燃料焚烧技术的研究现状及发展方向

固体回收燃料(SRF)是由城市生活垃圾(MSW)经机械生物处理(MBT)而得,具有高热值、低氯和含汞的特点,是继垃圾衍生燃料(RDF)之后的一种新型燃料。目前SRF焚烧技术在国内外已有一定的基础研究,但仍需要向大规模、高参数(高蒸汽温度和压力)、稳定运行方向发展。从垃圾焚烧现状入手,简述了国外SRF焚烧和共处置技术的研究现状,同时回顾了国内对MSW和RDF焚烧技术的相关研究,分析了SRF焚烧和共处置时污染物排放的规律,以及SRF对共处置锅炉运行工况的影响。最后指出了实现SRF焚烧技术的大规模、高参数工业应用必须研究的3个方面,包括:SRF的分类方法和燃烧模型,烟气净化系统的改进,SRF焚烧对锅炉腐蚀、结渣和积灰生长的影响。     

城市下水污泥焚烧过程中二次污染物排放特性的试验研究

在0．15MWt循环流化床燃烧试验台上进行了城市下水污泥与煤的混烧试验，分析了烟气中的二次污染物排放特性。分析结果表明，利用循环流化床焚烧城市下水污泥时，添加辅助燃料（如煤）及改变焚烧条件，不仅可以达到稳定燃烧的目的，而且有利于抑制焚烧中二次污染物（如CO及二恶英等有机污染物）的生成。分析了焚烧污泥污染物的排放特性。为采用焚烧方式处理城市下水污泥提供了基础性试验数据。     

欧洲MSW的焚烧处理

通过大量资料,对瑞士、西德、挪威、瑞典、丹麦等国MSW处理工艺的现状分析,可见焚烧技术已占优势,而未加处理的填埋正日趋减少。据丹麦有关方面研究,认为应先进行物质回收,而后再焚烧回收热能;应根据能量回收、环境效益、经济效益来评价焚烧工艺。挪     

垃圾焚烧重金属迁移特性及其影响因素

综述了城市固体垃圾（MSW）焚烧过程中的Hg、Cd、Pb、Cu,Zn,As和Cr等几种主要重金属污染源在焚烧过程中的迁移特性及其主要影响因素。将重金属在焚烧过程中的迂变归结为：蒸发、气相和表面反应、冷凝成核团聚和飞灰吸附等4个主要过程；而垃圾中重金属的初始浓度、原始垃圾的基体盐分（如Al、Si和K、Na等的存在形式）、垃圾中的C1（PVc和NaCl）和S的含量、垃圾的含水量以及焚烧过程中的运行参数（温度、滞留时间、氧化一还原气氛）等都会对焚烧过程的迁移规律产生影响。     

危险废物回转式流化冷渣多段焚烧系统焚烧特性研究

危险废物的处理和处置是摆在我国各级市政府面前的紧迫任务。然而我国已经运行的危险废物焚烧装置普遍存在回转窑挂壁结渣、热灼减率偏高和污染排放超标等问题,作者通过将回转窑和流化床特点相结合的方法提出了一种新型危险废物回转式流化冷渣多段焚烧处置装置。该装置采用回转窑(一燃室)、二燃室和流化床结合的热解-流化焚烧工艺,特别是采用控制窑头温度避免了回转窑挂壁结渣;采用流化冷渣装置延长未燃烬渣的焚烧时间,解决了热灼减率偏高问题;水冷式烟气急冷装置可以将烟气温度从1 100℃降到200℃,防止了二恶英的尾部低温再生成。该系统运行稳定可靠,可以处理医疗垃圾和大多数的固态和液态危险废物,实现了烟气污染物尤其是二恶英排放达到国家标准的目标。同时对该系统运行时窑头温度分布、二燃室炉膛出口氧量变化、回转窑和炉膛升温特性、燃烧室外壁温度分布等几方面运行数据都进行了详细的介绍,为危险废物焚烧炉的运行提供了宝贵的经验数据。     

控制燃油锅炉运行中NOx 生成的技术研究

分析燃油锅炉运行中NOx产生的机理，探讨影响其生成的因素，研究抑制其生成和排放的燃烧技术：低氧燃烧、掺水燃烧、空气分级燃烧和废气循环燃烧等。结合实验研究结果，重点分析空气分级燃烧和废气循环燃烧对油燃烧中燃料氮转化和氮氧化物生成的影响，并介绍一种新型低氮氧化物排放的燃油技术——预蒸发燃烧技术。     

城市下水污泥焚烧过程中二次污染物排放特性的试验研究

在0.15 MWt循环流化床燃烧试验台上进行了城市下水污泥与煤的混烧试验,分析了烟气中的二次污染物排放特性.分析结果表明,利用循环流化床焚烧城市下水污泥时,添加辅助燃料(如煤)及改变焚烧条件,不仅可以达到稳定燃烧的目的,而且有利于抑制焚烧中二次污染物(如CO及二恶英等有机污染物)的生成.分析了焚烧污泥污染物的排放特性,为采用焚烧方式处理城市下水污泥提供了基础性试验数据.     

氧富集技术用于污泥和固体废物焚烧

美国宾州Allen Town的空气产品公司开发了一种新的氧富集技术.采用这种技术,可在现有废料转化热能的焚烧工厂装置中将生活污水污泥和城市固体废物共同焚化,而对工厂只需作微小改革,而其燃烧状况和气体排放均无变化,故无需重新更换执照.实验室试验已证实如果燃烧气中氧富集量达27%(通常空气中含氧21%),则20%以上的脱水污泥和城市固体垃圾焚烧时,不会感到含酸气体排放量增加.该公司发言人期望该     

控制燃油锅炉运行中NOx生成的技术研究

分析燃油锅炉运行中NOx产生的机理,探讨影响其生成的因素,研究抑制其生成和排放的燃烧技术低氧燃烧、掺水燃烧、空气分级燃烧和废气循环燃烧等.结合实验研究结果,重点分析空气分级燃烧和废气循环燃烧对油燃烧中燃料氮转化和氮氧化物生成的影响,并介绍一种新型低氮氧化物排放的燃油技术--预蒸发燃烧技术.     

Evaluation of trichloroethene recovery processes in heterogeneous aquifer cells flushed with biodegradable surfactants

The ability of two biodegradable surfactants, polyoxyethylene (20) sorbitan monooleate (Tween 80) and sodium dihexyl sulfosuccinate (Aerosol MA), to recover a representative dense non-aqueous-phase liquid (DNAPL), trichloroethene (TCE), from heterogeneous porous media was evaluated through a combination of batch and aquifer cell experiments. An aqueous solution containing 3.3% Aerosol MA, 8% 2-propanol and 6 g/l CaCl(2) yielded a weight solubilization ratio (WSR) of 1.21 g TCE/g surfactant, with a corresponding liquid-liquid interfacial tension (IFT) of 0.19 dyn/cm. Flushing of aquifer cells containing a TCE-DNAPL source zone with approximately two pore volumes of the AMA formulation resulted in substantial (>30%) mobilization of TCE-DNAPL. However, a TCE mass recovery of 81% was achieved when the aqueous-phase flow rate was sufficient to displace the mobile TCE-DNAPL toward the effluent well. Aqueous solutions of Tween 80 exhibited a greater capacity to solubilize TCE (WSR=1.74 g TCE/g surfactant) and exerted markedly less reduction in IFT (10.4 dyn/cm). These data contradict an accepted empirical correlation used to estimate IFT values from solubilization capacity, and indicate a unique capacity of T80 to form concentrated TCE emulsions. Flushing of aquifer cells with less than 2.5 pore volumes of a 4% T80 solution achieved TCE mass recoveries ranging from 66 to 85%, with only slight TCE-DNAPL mobilization (<5%) occurring when the total trapping number exceeded 2 x 10(-5). These findings demonstrate the ability of Tween 80 and Aerosol MA solutions to efficiently recover TCE from a heterogeneous DNAPL source zone, and the utility of the total trapping number as a design parameter for a priori prediction of DNAPL mobilization and bank angle formation when flushing with low-IFT solutions. Given their potential to stimulate microbial reductive dechlorination at low concentrations, these surfactants are well-suited for remedial action plans that couple aggressive mass removal followed by enhanced bioremediation to treat chlorinated solvent source zones.     

The variation of street air levels of PAH and other mutagenic PAC in relation to regulations of traffic emissions and the impact of atmospheric processes

The occurrence of particle associated PAH and other mutagenic PAC was determined in 1996 in the street air of Copenhagen. In addition, particle extracts were tested for mutagenicity. The measurements were compared with previous measurements in 1992/1993. The levels had decreased in this period. The decrease was caused by an implementation of light diesel fuels for buses and the exchange of older petrol-driven passenger cars with catalystequipped new ones. About 65% of the reduction was caused by the application of the light diesel fuels. Under special conditions, chemical processes in the atmosphere produced many more mutagens than the direct emissions. The concentrations of S-PAC and N-PAC were 10 times lower than those of PAH, while the levels of oxy-PAH were in the same order of magnitude as those of PAH. Benzanthrone, an oxy-PAH, is proposed to be formed in the atmosphere in addition to direct emissions. Benzo(a)pyrene, often applied as an air quality criteria indicator, was photochemically degraded in the atmosphere. A strong increase in the mutagenic activities was observed to coincide with a depletion of benzo(a)pyrene.     

Chloroaromatic pollutants in mussels incubated in two finnish watercourses polluted by industry

Concentrations of different chlorinated compounds were measured in mussels incubated in two polluted watercourses, a river (the River Kymijoki) and a lake (Lake Vanaja) for four weeks in summer 1995. The sum concentrations of polychlorinated phenols (PCP) and biphenyls (PCB) were both about 1 μg/g lipid weight (lw) in Lake Vanaja mussels, while in the River Kymijoki mussels PCPs were non-detectable and PCBs were measured 120 ng/g lIw. The concentrations of toxic polychlorinated dibenzo-p-dioxin (PCDD) and dibenzofuran (PCDF) congeners ranged between <17 and 370 pg/g Iw in Lake Vanaja mussels and between <38 and 11,000 pg/g lw in the River Kymijoki mussels. Polychlorinated diphenyl ethers (PCDE) were detected in the mussels incubated in the River Kymijoki (0.4–1.1 ng/g Iw), but not in those incubated in Lake Vanaja. Polychlorinated phenoxyanisoles (PCPA) were measured 33 ng/g lw and polychlorinated phenoxyphenols (PCPP) 300 ng/g lw in the mussels incubated in the River Kymijoki. PCPAs were also detected in reference samples, which were sediment and pike from the River Kymijoki and Baltic salmon, seal and white-tailed sea eagle.     

Teratological effects of pesticides in vertebrates: a review

Abstract

In the last decades, the use and misuse of pesticides in the agriculture have increased, having a severe impact on ecosystems and their fauna. Although the various effects of pesticides on biodiversity have been already documented in several studies, to our knowledge no consistent overview of the impact of pesticides in vertebrates, both terrestrial and aquatic, is available. In this review, we try to present a concise compilation of the teratogenic effects of pesticides on the different classes of vertebrates – mammals, birds, reptiles, amphibians and fish.     

Book review

The Pesticide Manual ‐ A World Compendium, 8th Edition, C.R. Worthing, Editor and S.B. Walker, Assistant Editor, British Crop Protection Council, BCPC Publications Sales, Bear Farm, Binfield, Bracknell, Berkshire RG12 5QE, England. 1987, 1100 pp., UK £50; Overseas £56. ISBN 0–948404–01–9.     

Patterns of volatile metabolites and nonvolatile trichothecenes produced by isolates of <Emphasis Type="Italic">Stachybotrys,Fusarium, Trichoderma,Trichothecium</Emphasis> and <Emphasis Type="Italic">Memnoniella</Emphasis>

We reported previously that trichodiene, a volatile trichothecene derivative, was produced by a Stachybotrys isolate, also known to produce highly cytotoxic, non-volatile, macrocyclic trichothecenes (satrotoxins). We investigated the relationship between the production of trichodiene and various non-volatile trichothecenes for several molds. Volatile metabolites were concentrated by adsorption on Tenax TA and analyzed by GC/MS, while non-volatile metabolites were separated by HPLC, derivatized and analyzed by GC/MS. Stachybotrys chartarum isolates producing macrocyclic trichothecenes secreted significantly larger amounts of trichodiene and other sesquiterpenes than isolates which only produced simple trichothecenes. The amounts of secreted trichodiene were relatively small in all cases. With the exception of Memnoniella, which excreted small amounts of sesquiterpenes, the other isolates produced varying amounts of sesquiterpenes, including trichodiene, as well as simple tricothecenes, no detectable trichodiene, but large amounts of griseofulvin derivatives. In Stachybotrys there is apparently a correlation between trichodiene and macrocyclic trichothecene production. In the remaining isolates, there was no simple relationship between trichodiene and non-volatile trichothecene synthesis. Trichodiene is produced in larger amounts by Stachybotrys isolates, which also produce satratoxins, but it will be difficult to utilize this metabolite to detect toxic isolates in buildings due to the relatively small amounts excreted.     

Observations on the influence of water and soil pH on the persistence of insecticides

Abstract

The pH‐disappearance rate profiles were determined at ca. 25°C for 24 insecticides at 4 or 5 pH values over the range 4.5 to 8.0 in sterile phosphate buffers prepared in water‐ethanol (99: 1 v/v). Half‐lives measured at pH 8 were generally smaller than at lower pH values. Changes in half lives between pH 8.0 and 4.5 were largest (>1000x) for the aryl carbamates, carbofuran and carbaryl, the oxime carbamate, oxamyl, and the organophosphorus insecticide, trichlorfon. In contrast, half lives of phorate, terbufos, heptachlor, fensulfothion and aldicarb were affected only slightly by pH changes. Under the experimental conditions described half lives at pH8 varied from 1–2 days for trichlorfon and oxamyl to >1 year for fensulfothion and cyper‐methrin. Insecticide persistence on alumina (acid, neutral and basic), mineral soils amended with aluminum sulfate or calcium hydroxide to different pH values and four natural soils of different pH was examined. No correlation was observed between the measured pH of these solids and the rate of disappearance of selected insecticides applied to them. These observations demonstrate the difficulty of extrapolating the pH dependent disappearance behaviour observed in homogeneous solution to partially solid heterogeneous systems such as soil.     

Knowledge transfer initiative between molecular biologists and environmental researchers and regulators

A Natural Environment Research Council (NERC) funded Knowledge Transfer (KT) workshop was held in the United Kingdom (UK) to identify the needs and opportunities in the application of molecular biology and ‘omics’ techniques to environmental monitoring and risk assessment. Attendees highlighted a lack of effective communication between end-users and researchers as well as difficulties with data interpretation as reasons behind the slow uptake of molecular biology and omics techniques. A number of promising areas in which new techniques could be implemented at a practical level in the very near future were identified, thereby raising the profile of these recent technologies and providing vital proof of concept work. Molecular taxonomy, bacterial source tracking and pre-screening of chemicals for potential toxicities were all viewed as areas in which omics and molecular techniques could have immediate value, with the aim of reducing cost, increasing efficiency and providing more comprehensive data of improved quality.     

Sorption and predicted mobility of herbicides in Baltic soils

This study was undertaken to determine sorption coefficients of eight herbicides (alachlor, amitrole, atrazine, simazine, dicamba, imazamox, imazethapyr, and pendimethalin) to seven agricultural soils from sites throughout Lithuania. The measured sorption coefficients were used to predict the susceptibility of these herbicides to leach to groundwater. Soil-water partitioning coefficients were measured in batch equilibrium studies using radiolabeled herbicides. In most soils, sorption followed the general trend pendimethalin > alachlor > atrazine～ amitrole～ simazine > imazethapyr > imazamox > dicamba, consistent with the trends in hydrophobicity (log K_ow) except in the case of amitrole. For several herbicides, sorption coefficients and calculated retardation factors were lowest (predicted to be most susceptible to leaching) in a soil of intermediate organic carbon content and sand content. Calculated herbicide retardation factors were high for soils with high organic carbon contents. Estimated leaching times under saturated conditions, assuming no herbicide degradation and no preferential water flow, were more strongly affected by soil textural effects on predicted water flow than by herbicide sorption effects. All herbicides were predicted to be slowest to leach in soils with high clay and low sand contents, and fastest to leach in soils with high sand content and low organic matter content. Herbicide management is important to the continued increase in agricultural production and profitability in the Baltic region, and these results will be useful in identifying critical areas requiring improved management practices to reduce water contamination by pesticides.     

The chemical stability of formulations of some hydrolyzable insecticides in aqueous mixtures with hydrolysis catalysts

Abstract

The active ingredients in commercial formulations of malathion, oxamyl, carbaryl, diazinon, and chlorpyrifos diluted to “spray tank”; concentrations with buffered distilled or natural water of pH 4–9 were stable for at least 24 hr. Formulations of trichlorfon were not stable at pH 7 or above but disappearance rates were slower than for the pure chemical in homogeneous solution. Cupric ion was observed to be an effective catalyst for the hydrolysis of a variety of pure organophosphorus insecticides but did not catalyze hydrolysis of the active ingredients of the formulations examined. Increasing the dilution of the formulation increased the susceptibility of malathion, oxamyl, and carbaryl to hydrolysis.