含油污泥处理技术进展

对国内外含油污泥的处理技术作一简述,介绍了含油污泥的调质－机械分离处理技术,高温处理技术,溶剂萃取处理技术和综合利用技术。     

微污染水源水的控制技术

饮用水水源的污染日益严重,对人类的健康和传统净水工艺都构成了较大的威胁,更加剧了水资源的危机,文中阐述了近年来我国处理微污染水源水的主要技术,强化混凝处理技术,臭氧活性炭联用深度处理技术,生物活性炭深度处理技术,光催化氧化法技术,膜法深度处理技术,吸附预处理技术,生物预处理技术等,并给出了各种处理方法的优缺点。     

废水深度处理技术研究的现状和发展

综述了近年流行的废水深度处理技术，阐述了各种技术的原理和优缺点，为深度处理技术的研究和新工艺的开发提供参考。深度处理技术将是未来我国水处理的主要发展方向，文中展望了一些技术的发展和应用。     

生活垃圾填埋场渗滤液处理技术研究

根据处理工艺原理的不同 ,分别介绍生化和物化处理技术、膜处理技术、土地处理技术和蒸发处理技术等处理工艺研究与应用的进展情况 ,同时根据我国填埋场渗滤液的产生特点和处理处置现状 ,展望了我国渗滤液处理工艺的发展趋势。     

生活垃圾填埋场渗滤液处理技术研究

根据处理工艺原理的不同，分别介绍生化和物化处理技术、膜处理技术、土地处理技术和蒸发处理技术等处理工艺研究与应用的进展情况，同时根据我国填埋场渗滤液的产生特点和处理处置现状，展望了我国渗滤液处理工艺的发展趋势。     

工业循环冷却水处理技术研究动态

目前工业循环水处理技术主要有药剂处理、磁化处理和臭氧处理,其中药剂处理最为常用。近年来,药剂作用机理研究日趋深化,药剂合成、检验与复配技术也得到较大发展;同时,水处理技术的发展为循环水水质稳定技术注入了新的活力,磁化处理、臭氧处理技术也相继运用到工业循环水处理技术中来,并取得了较好效果。     

低温等离子体处理废液技术研究概述

低温等离子体技术包括热等离子体技术和冷等离子体技术。该技术处理废液具有范围广、快速、高效、无二次污染等优点,尤其对难降解有毒废液的处理,其先进性和优越性更为突出,被认为是21世纪环境污染物处理领域中最有发展前途的新技术之一。综述了低温等离子体处理废液技术的研究和进展,重点分析了冷等离子体技术处理难降解有机废液的作用机理,探讨了其现存的主要问题,并指出了今后需要研究的方向。     

深井灌注技术处理高盐废水的可行性分析

简要介绍了高盐废水的概念、危害和传统的处理技术,分析了当前高盐废水处理技术面临的瓶颈。在此基础上提出了深井灌注处理高盐废水技术,概括了深井灌注的国内外发展状况,分析了该技术的应用条件和环境风险,讨论了中国采用深井灌注技术处理高盐废水的可行性。     

农药生产废水处理方法与资源化技术

综述了农药生产废水的常用处理方法和资源化技术 ,认为在处理废水的同时 ,应尽可能地回收和利用废水中有用物质 ;同时 ,要合理采用综合处理技术 ,以期达到最佳的处理效果     

农药生产废水处理方法与资源化技术

综述了农药生产废水的常用处理方法和资源化技术，认为在处理废水的同时，应尽可能地回收和利用废水中有用物质；同时，要合理采用综合处理技术，以期达到最佳的处理效果。     

生物法处理NOx废气的研究进展

氮氧化物 (NOx)是主要的大气污染物之一 ,是治理大气污染的一大难题。对当前国内外生物处理NOx 的研究现状进行了系统的论述 ,介绍了生物过滤法处理氮氧化物的基本原理 ,分析了生物过滤法处理氮氧化物存在的问题 ,并预测该技术的未来发展趋势     

Acceleration of the Fe(III)EDTA(-) reduction rate in BioDeNO(x) reactors by dosing electron mediating compounds

BioDeNO(x), a novel technique to remove NO(x) from industrial flue gases, is based on absorption of gaseous nitric oxide into an aqueous Fe(II)EDTA(2-) solution, followed by the biological reduction of Fe(II)EDTA(2-) complexed NO to N(2). Besides NO reduction, high rate biological Fe(III)EDTA(-) reduction is a crucial factor for a succesful application of the BioDeNO(x) technology, as it determines the Fe(II)EDTA(2-) concentration in the scrubber liquor and thus the efficiency of NO removal from the gas phase. This paper investigates the mechanism and kinetics of biological Fe(III)EDTA(-) reduction by unadapted anaerobic methanogenic sludge and BioDeNO(x) reactor mixed liquor. The influence of different electron donors, electron mediating compounds and CaSO(3) on the Fe(III)EDTA(-) reduction rate was determined in batch experiments (21mM Fe(III)EDTA(-), 55 degrees C, pH 7.2+/-0.2). The Fe(III)EDTA(-) reduction rate depended on the type of electron donor, the highest rate (13.9mMh(-1)) was observed with glucose, followed by ethanol, acetate and hydrogen. Fe(III)EDTA(-) reduction occurred at a relatively slow (4.1mMh(-1)) rate with methanol as the electron donor. Small amounts (0.5mM) of sulfide, cysteine or elemental sulfur accelerated the Fe(III)EDTA(-) reduction. The amount of iron reduced significantly exceeded the amount that can be formed by the chemical reaction of sulfide with Fe(III)EDTA(-), suggesting that the Fe(III)EDTA(-) reduction was accelerated via an auto-catalytic process with an unidentified electron mediating compound, presumably polysulfides, formed out of the sulfur additives. Using ethanol as electron donor, the specific Fe(III)EDTA(-) reduction rate was linearly related to the amount of sulfide supplied. CaSO(3) (0.5-100mM) inhibited Fe(III)EDTA(-) reduction, probably because SO(3)(2-) scavenged the electron mediating compound.     

锅炉烟气联合脱硫脱氮技术

硫氧化物和氮氧化物是燃煤锅炉排放的主要污染物 ,传统分步脱硫脱氮设备昂贵且效率不高 ,而联合脱硫脱氮技术具有很大的优越性 ,如可以减小系统的复杂性、具有更好的运行性能、较低的成本及较小的占地面积 ,因此实现在一个系统内同时脱硫脱氮的工艺成为国内外烟气净化技术的研究重点。对近年来国内外各种联合脱硫脱氮技术的脱除原理、研究现状、应用情况和主要优缺点进行了论述 ,并对各工艺的经济技术指标给予了多方面的比较。通过对两类烟气联合脱硫脱氮技术 (炉内联合脱除和烟气中联合脱除 )的分析、综合和比较 ,找出了我国今后脱硫脱氮技术的研究重点 ,从而为脱硫脱氮技术的进一步开发和改进提供参考     

The importance of the location of sodium chlorite application in a multipollutant flue gas cleaning system

In this study, removing sulfur dioxide (SO2), nitrogen oxides (NO(x)), and mercury (Hg) from simulated flue gas was investigated in two laboratory-sized bubbling reactors that simulated an oxidizing reactor (where the NO and Hg(0) oxidation reactions are expected to occur) and a wet limestone scrubber, respectively. A sodium chlorite solution was used as the oxidizing agent. The sodium chlorite solution was an effective additive that enhanced the NO(x), Hg, and SO2 capture from the flue gas. Furthermore, it was discovered that the location of the sodium chlorite application (before, in, or after the wet scrubber) greatly influences which pollutants are removed and the amount removed. This effect is related to the chemical conditions (pH, absence/presence of particular gases) that are present at different positions throughout the flue gas cleaning system profile. The research results indicated that there is a potential to achieve nearly zero SO2, NO(x), and Hg emissions (complete SO2, NO, and Hg removals and -90% of NO(x) absorption from initial values of 1500 ppmv of SO2, 200 ppmv of NO(x), and 206 microg/m3 of Hg(0)) from the flue gas when sodium chlorite was applied before the wet limestone scrubber. However applying the oxidizer after the wet limestone scrubber was the most effective configuration for Hg and NO(x) control for extremely low chlorite concentrations (below 0.002 M) and therefore appears to be the best configuration for Hg control or as an additional step in NO(x) recleaning (after other NO(x) control facilities). The multipollutant scrubber, into which the chlorite was injected simultaneously with the calcium carbonate slurry, appeared to be the least expensive solution (when consider only capital cost), but exhibited the lowest NO(x) absorption at -50%. The bench-scale test results presented can be used to develop performance predictions for a full- or pilot-scale multipollutant flue gas cleaning system equipped with wet flue gas desulfurization scrubber.     

用活性填料催化氧化-硝酸吸收法脱除氮氧化物的研究

为了提高硝酸吸收氮氧化物的效率，对活性填料催化氧化-硝酸吸收NOx进行了研究。结果表明：活性填料能明显提高NOx的吸收效率；当NOx中NO2体积百分含量增加，其吸收效率增加；随进气浓度和液气比的增大，NOx吸收效率增加；随NO2浓度的增加，NO的吸收效率先增加后减少，在NO／NO2为3时，NO吸收效率最高；随NO的增加NO2的吸收效率先增加后减少，在NO／NO2为0．6～1之间，NO2的吸收效果较好。     

Transformations,Lifetimes, and Sources of NO2, HONO,and HNO3 in Indoor Environments

Recent research has demonstrated that nitrogen oxides are transformed to nitrogen acids in indoor environments, and that significant concentrations of nitrous acid are present in indoor air. The purpose of the study reported in this paper has been to investigate the sources, chemical transformations and lifetimes of nitrogen oxides and nitrogen acids under the conditions existing in buildings. An unoccupied single family residence was instrumented for monitoring of NO, NO₂, NO_y, MONO, HNO₃, CO, temperature, relative humidity, and air exchange rate. For some experiments, NO₂ and HONO were injected into the house to determine their removal rates and lifetimes. Other experiments investigated the emissions and transformations of nitrogen species from unvented natural gas appliances. We determined that HONO is formed by both direct emissions from combustion processes and reaction of NO₂ with surfaces present indoors. Equilibrium considerations influence the relative contributions of these two sources to the indoor burden of HONO. We determined that the lifetimes of trace nitrogen species varied in the order NO ~ HONO > NO₂ >HNO₃. The lifetimes with respect to reactive processes are on the order of hours for NO and HONO, about an hour for NO₂, and 30 minutes or less for HNO3. The rapid removal of NO₂ and long lifetime of HONO suggest that HONO may represent a significant fraction of the oxidized nitrogen burden in indoor air.     

Evaluation of NO(x) flue gas analyzers for accuracy and their applicability for low-concentration measurements

The requirements of the Texas State Implementation Plan of the U.S. Clean Air Act for the Houston-Galveston Ozone Nonattainment Area stipulate large reductions in oxides of nitrogen (NO(x)) emissions. A large number of sources at Dow Chemical Co. sites within the nonattainment area may require the addition of continuous emission monitoring systems (CEMS) for online analysis of NO(x), CO, and O2. At the outset of this work, it was not known whether the analyzers could accurately measure NO(x) as low as 2 ppm. Therefore, NO(x) CEMS analyzers from five different companies were evaluated for their ability to reliably measure NO(x) in the 2-20 ppm range. Testing was performed with a laboratory apparatus that accurately simulated different mixtures of flue gas and, on a limited basis, simulated a dual-train sampling system on a gas turbine. The results indicate that this method is a reasonable approach for analyzer testing and reveal important technical performance aspects for accurate NO(x) measurements. Several commercial analyzers, if installed in a CEMS application with sampling conditioning components similar to those used in this study, can meet the U.S. Environmental Protection Agency's measurement data quality requirements for accuracy.     

用活性填料催化氧化-硝酸吸收法脱除氮氧化物的研究

为了提高硝酸吸收氮氧化物的效率,对活性填料催化氧化-硝酸吸收NOx进行了研究.结果表明:活性填料能明显提高NOx的吸收效率;当NOx中NO2体积百分含量增加,其吸收效率增加;随进气浓度和液气比的增大,NOx吸收效率增加;随NO2浓度的增加,NO的吸收效率先增加后减少,在NO/NO2为3时,NO吸收效率最高;随NO的增加NO2的吸收效率先增加后减少,在NO/NO2为0.6～1之间,NO2的吸收效果较好.     

水吸收法处理低浓度氮氧化物废气的中试研究

对水在中试规模下吸收低浓度的氮氧化物废气进行了研究。分别研究了喷淋密度、温度、压力、气速以及氮氧化物浓度对吸收效果的影响,结果表明,综合考虑各种因素,喷淋密度在20 m3/（m2·h）,水温在15℃以下,气速小于0.28 m/s,废气浓度在400 mg/m3左右时,氮氧化物的平均脱除率可以达到50%左右;同时,随着压力的增大,吸收效率也增加。     

Responses of spruce seedlings (Picea abies) to exhaust gas under laboratory conditions--I. Plant-insect interactions

The effects of motor vehicle exhaust gas on Norway spruce seedlings (Picea abies (L.) Karst) and plant-insect interaction of spruce shoot aphid (Cinara pilicornis Hartig) was studied. The exhaust gas concentrations in the fumigation chambers were monitored and controlled by measuring the concentration of nitrogen oxides (NO(x)) with a computer aided feedback system. The concentrations of major exhaust gas components (black carbon [BC], fine particles, VOCs and carbonyl compounds) in the chamber air were also measured. Responses of Norway spruce seedlings to a 2 and 3-week exhaust gas exposure and subsequent performance of spruce shoot aphid were studied using realistic exposure regimes; 50, 100 and 200 ppb NO(x). The feedback control system based on NO(x) concentrations proved an adequate and practical means for controlling the concentration of exhaust gases and studying plant responses in controlled environment chambers. The exhaust exposure resulted in increased concentrations of proline, glutamine, threonine, aspartic acid, glycine and phenylalanine and decreased concentration of arginine, serine, alanine and glycine in young needles. No changes in soluble N concentrations were observed. The results are interpreted as a stress response rather than use of NO(x) as a nitrogen source. No changes in total phenolics and only transient changes in some individual terpene concentrations were detected. The exhaust gas exposure stressed the exposed seedlings, but had no significant effect on N metabolism or the production of defence chemicals. Aphid performance was not significantly affected. Soluble N, secondary metabolism and aphid performance were not sensitive to exhaust gas exposure during shoot elongation in Norway spruce.