湿式电除尘技术及其在电厂的应用前景探讨

作为大气复合污染物控制系统的终瑞精处理技术装备,湿式电除尘器可用于控制PM2.5、酸雾、气溶胶、亚微米颗粒物、汞、重金属及二恶英等污染物的排放。论述了湿式电除尘器的工作原理、技术特点、结构及设计形式,探讨了湿式电除尘器在我国燃煤电厂的应用前景。     

600 MW机组除尘器升级改造及效益评价

元宝山发电有限责任公司2号600 MW机组配套电除尘器由于设计效率低、燃烧煤种变化、设备老化等多方面原因,除尘效率下降,除尘器出口烟尘排放浓度超标严重。为了满足新的《火电厂大气污染物排放标准》的要求,对元宝山发电有限责任公司2号机组配套电除尘器进行升级改造,将原有的4台四电场静电除尘器增效改造为4台电袋复合式除尘器。通过电除尘器的改造,降低了除尘器出口粉尘排放浓度,提高了除尘效率,保证了2号机组电除尘器的安全稳定运行。     

内地与香港燃煤电厂大气污染物排放控制政策与标准比较

香港特区与广东省政府联合成立粤港持续发展与环保合作小组,并发表《改善珠江三角洲空气质量的联合声明》（简称＂减排联合声明＂）,同意制定合理的减排方案,共同执行管理计划。总结分析了粤、港地区在治理燃煤电厂大气污染物方面的控制政策,并对大陆与香港特区燃煤电厂大气污染物的排放标准进行比较。     

燃煤电厂烟尘超低排放技术措施研究

针对越来越严格的环保要求,介绍了原有的除尘技术,并对除尘器新技术改造方案进行了说明,其中重点对电袋复合代替静电除尘技术、在静电除尘器中增置旋转电极、更改工频电源为高频电源、在电除尘器前加装低温换热器、脱硫后增加湿式电除尘器技术等方案进行比较分析。为了达到超低排放要求,对不同的烟尘超低排放实践工艺进行了说明,并结合东部沿海地区可再生能源发展空间有限的实际情况,提出加快推广超低排放技术在现有燃煤电厂的应用,实现传统煤电产业和环保产业的转型升级。     

欧盟国家燃煤电厂环保政策及技术路线分析

温室气体的排放控制作为全球性的环境问题受到了广泛关注。中国是火力发电的大国,其燃煤机组的温室气体排放总量巨大。《火电厂大气污染物排放标准》（GB 13223-2011）提高了我国燃煤电厂的烟气污染物排放的要求,对火电厂烟气处理的技术选择和投资都会产生重大影响。针对中国燃煤电厂环保面临的新形势,阐述了欧盟国家的环保政策重点,并对欧盟国家燃煤电厂污染物控制的相关标准进行了分析,同时简要介绍了欧盟国家燃煤电厂环保的主要技术路线,在一定程度上可作为中国燃煤电厂污染物控制的借鉴和参考。     

高频电源在660 MW机组电除尘器中的应用

新的《火电厂大气污染物排放标准》（ GB 13223-2011）对燃煤发电厂的烟尘排放浓度作出了更为严格的限制,重点地区烟尘排放标准由50 mg/m3变为30 mg/m3。目前,国内部分火力发电厂电除尘器很难达到新标准要求。针对上述问题,某电厂对电除尘器进行了高频电源改造。介绍高频电源的工作原理,分析高频电源替代传统的工频电源方案的可行性,并以基建实例简要介绍工频电源改为高频电源的措施,实现节约基建成本,达到节能减排目的。     

发电集团应对燃煤电厂超低排放的思考

新的《火电厂大气污染排放标准》全面加大了对火电厂大气污染物中烟尘、SO2、NOx的控制力度,收严了污染物排放限值。近期提出的煤电节能减排升级与改造行动计划,进一步提出了燃煤电厂达到燃气机组排放标准的超低排放要求。解读了燃煤电厂推行超低排放的一些政策支撑、技术路线,从华电集团超低排放技术及应用实例出发,对超低排放技术实施过程中需要关注的问题进行了探讨,具有一定的参考价值。     

适应低排放的电除尘技术探讨

针对高标准的排放要求以及将进一步提高的排放标准,对电除尘器是否能满足目前的排放标准和低排放要求进行了研究。通过对国内110个机组配套电除尘器实际应用情况调查和国外燃煤机组电除尘器应用分析,客观地评价了电除尘器对国内煤种的适应性,指出移动电极式电除尘器、双极异距电流体微粒聚合器、烟气调质、湿式电除尘器、低低温电除尘器等新技术的发展和综合应用是满足30mg/m3低排放标要求的最佳选择。     

燃煤电厂汞排放分析及控制技术研究

新的《火电厂大气排放标准》的颁布实施,燃煤电厂汞的排放正式纳入控制标准。针对目前我国燃煤电厂汞排放化学形态转换、排放特征,分析和总结现有污染控制设施对汞协同控制效果,提出适合我国国情的燃煤电厂汞控制技术措施的建议及发展趋势,可有效控制燃煤电厂汞的排放量。     

电除尘器改造为电袋复合除尘器的实践

介绍了扬子热电厂1~7号炉电除尘器改造为电袋复合除尘器的工程实践,分析了电袋复合除尘器的关键技术及运行情况。改造后,电袋复合除尘器出口烟尘浓度≤30mg/m3,满足排放要求。     

Distribution of Cd,Ck, Pb and Zn in Soil and Vegetation Compartments in Stands of Five Boreal Tree Species in N.E. Sweden

Concentrations and total quantity of cadmium (Cd), cupper (Cu),lead (Pb) and zink (Zn) were determined in biomass and soil compartments in a replicated tree species experiment with 27-yr-old stands growing on former farmland in N.E. Sweden. Sequentialextractions of soil samples were performed in order to estimate the exchangeable and an organically bound fraction of each element. The tree species included were Picea abies (L.)H. Karst., Pinus sylvestris L., Pinus contorta Dougl., Larix sibirica Ledeb., and Betula pendula Roth.Tree species influenced the rate of removal of Cu, Pb and Zn incase of stemwood harvesting, and of Cd, Cu and Zn in the case ofwhole-tree harvesting. B. pendula and P. abies had higher quantities and average concentrations of Zn in the biomass. For all species, >50% of the Zn in the stems was found in the bark. P. abies and L. sibirica had higher quantities of Cu in the biomass than the other species.P. abies and P. contorta had high quantities of Cd inthe biomass in relation to the other species. Branches and stembark contained high concentrations of Cd and Pb in relation to foliage and stemwood. Dead branches had especially high concentrations of Pb. The high accumulation rate of Zn in thebiomass of B. pendula was related to a low exchangeable amount of Zn in the A horizon. In the superficial centimeters ofthe A horizon, a depletion similar to that found for Zn was detected for Cu, whereas for Cd and Pb, no correlations were found between quantities of elements in the trees and element pools in the soil.     

Starch-plastic materials—Preparation,physical properties,and biodegradability (a review of recent USDA research)

Recent starch-plastic research at the National Center for Agricultural Utilization Research is reviewed and related worldwide efforts are noted. Properties of starch that influence its formulation and performance in plastics are discussed. Methods are given for preparation of starch-poly(methyl acrylate) graft copolymer, starch-poly(ethylene-co-acrylic acid), and starch-poly(ethylene-co-acrylic acid)-polyethylene plastics. Their physical properties are discussed, as is degradability by enzymes or amylolytic organisms from soil, ponds, and streams.The mention of firm names or trade products does not imply that they are endorsed or recommended by the U.S. Department of Agriculture over other firms or similar products not mentioned.     

Application of Cellulose Microfibrils in Polymer Nanocomposites

Cellulose microfibrils obtained by the acid hydrolysis of cellulose fibers were added at low concentrations (2–10% w/w) to polymer gels and films as reinforcing agents. Significant changes in mechanical properties, especially maximum load and tensile strength, were obtained for fibrils derived from several cellulosic sources, including cotton, softwood, and bacterial cellulose. For extruded starch plastics, the addition of cotton-derived microfibrils at 10.3% (w/w) concentration increased Young’s modulus by 5-fold relative to a control sample with no cellulose reinforcement. Preliminary data suggests that shear alignment significantly improves tensile strength. Addition of microfibrils does not always change mechanical properties in a predictable direction. Whereas tensile strength and modulus were shown to increase during addition of microfibrils to an extruded starch thermoplastic and a cast latex film, these parameters decreased when microfibrils were added to a starch–pectin blend, implying that complex interactions are involved in the application of these reinforcing agents.     

四氮唑废水处理工艺设计

高浓度、高盐分的四氮唑生产废水通过三效蒸发浓缩,馏出液经铁炭氧微电解和混凝预处理,再采用水解酸化一接触氧化一反应二沉主体组合工艺进行处理。研究了该工艺所需构筑物和设备的设计与选型。该工艺在正常运行条件下,处理后出水pH6～9,COD 302mg／L,BOD5 108mg／L,SS30mg／L,色度36倍,水质达到GB8978--1996（污水综合排放标准》三级标准。     

Bioassessment of silvicultural impacts in streams and wetlands of the Eastern United States

Bioassessment is a useful tool to determine the impact of logging practices on the biological integrity of streams and wetlands. Measuring biota directly has an intuitive appeal for impact assessment, and biota can be superior indicators to physical or chemical characteristics because they can reflect cumulative impacts over time. Logging can affect stream and wetland biota by increasing sedimentation rates, altering hydrologic, thermal, and chemical regimes, and changing the base of food webs. Biotic impacts of logging on streams compared to wetlands probably differ, and in this paper we review some of those differences. In streams, invertebrates, fishes, amphibians, algae, and macrophytes have been used as indicators of logging impacts. In wetlands, bioassessment is just beginning to be used, and plants and birds are the most promising indicator taxa. Various best management practices (BMPs) have been developed to reduce the impacts of logging on stream and wetland biota, and we review quantitative studies that have evaluated the efficacy of some of these techniques in streams and wetlands in the eastern United States. Remarkably few studies that address the overall efficacy of BMPs in limiting biotic changes in streams and wetlands after BMP implementation have been published in scientific journals, although some work exists in reports or is unpublished. We review these works, and compile conclusions about BMP efficacy for biota from this body of research.     

Characterization of air emissions and residual ash from open burning of electronic wastes during simulated rudimentary recycling operations

Air emissions and residual ash samples were collected and analyzed during experiments of open, uncontrolled combustion of electronic waste (e-waste), simulating practices associated with rudimentary e-waste recycling operations. Circuit boards and insulated wires were handled separately to simulate processes associated with metal recovery. The average emissions of polychlorinated dibenzodioxins and dibenzofurans (PCDD/PCDFs) were 92 ng toxic equivalency (TEQ)/kg [n = 2, relative standard deviation (RSD) = 98%] and 11 900 ng TEQ/kg (n = 3, RSD = 50%) of the initial mass of the circuit boards and insulated wire, respectively. The value for the insulated wire is about 100 times higher than that for backyard barrel burning of domestic waste. The emission concentrations of polybrominated dibenzodioxins and dibenzofurans (PBDD/PBDFs) from the combustion of circuit boards were 100 times higher than for their polychlorinated counterparts. Particulate matter (PM) sampling of the fly ash emissions indicated PM emission factors of approximately 15 and 17 g/kg of the initial mass for the circuit boards and insulated wire, respectively. Fly ash samples from both types of e-waste contained considerable amounts of several metallic elements and halogens; lead concentrations were more than 200 times the United States regulatory limits for municipal waste combustors and 20 times those for secondary lead smelters. Leaching tests of the residual bottom ash showed that lead concentrations exceeded U.S. Environmental Protection Agency landfill limits, designating this ash as a hazardous waste.     

Does Soil Acidification Affect Spruce Needle Chemical Composition and Tree Growth?

In 1994, a large survey of soil chemistry was undertaken in thecounty of Värmland in central Sweden (Lundström et al., 1998).The southern part of the county was affected by soilacidification whereas there were no such indications in thenorthern part. To investigate the influence of soil chemistryon the trees at the specific sites, the survey was continued byan analysis of needle chemistry (Norway spruce) which wasundertaken at 150 of the 180 sites, and of tree growth at 65 ofthe 180 sites. Growth was expressed as a ratio between expectedgrowth, estimated with a national, empirical growth model, andthe growth observed in the field. In statistical analyses,using rank correlation, PCA and PLS, there were only weakindications of an influence of soil chemistry on needlechemistry and on tree growth. A moderate correlation betweennitrogen and sulphur in needles was found, which wasinterpreted as an effect of deposition and of processes in thetree canopy. No obvious regional pattern of the growth ratiowas found, in contrast to the clear pattern of soilacidification. The statistical analysis could not with anycertainty point out any of the soil chemistry variables asespecially important for the tree growth ratio.     

Solubility and Potential Mobility of Heavy Metals in Two Contaminated Urban Soils from Stockholm,Sweden

The solubility and potential mobility of heavy metals (Cd, Cu,Hg, Pb and Zn) in two urban soils were studied by sequential andleaching extractions (rainwater). Compared to rural (arable) soils on similar parent material, the urban soils were highlycontaminated with Hg and Pb and to a lesser extent also with Cd,Cu and Zn. Metal concentrations in rainwater leachates were related to sequential extractions and metal levels reported fromStockholm groundwater. Cadmium and Zn in the soils were mainly recovered in easily extractable fractions, whereas Cu and Pb were complex bound. Concentrations of Pb in the residual fractionwere between two- and eightfold those in arable soils, indicatingthat the sequential extraction scheme did not reflect the solidphases affected by anthropogenic inputs. Cadmium and Zn conc. inthe rainwater leachates were within the range detected in Stockholm groundwater, while Cu and Pb conc. were higher, whichsuggests that Cu and Pb released from the surface soil were immobilised in deeper soil layers. In a soil highly contaminatedwith Hg, the Hg conc. in the leachate was above the median concentration, but still 50 times lower than the max concentration found in groundwater, indicating the possibilityof other sources. In conclusion, it proved difficult to quantitatively predict the mobility of metals in soils by sequential extractions.     

Biodegradation of Injection Molded Starch-Poly (3-hydroxybutyrate-co-3-hydroxyvalerate) Blends in a Natural Compost Environment

Injection molded specimens were prepared by blending poly (hydroxybutyrate-co-valerate) (PHBV) with cornstarch. Blended formulations incorporated 30% or 50% starch in the presence or absence of poly-(ethylene oxide) (PEO), which enhances the adherence of starch granules to PHBV. These formulations were evaluated for their biodegradability in natural compost by measuring changes in physical and chemical properties over a period of 125 days. The degradation of plastic material, as evidenced by weight loss and deterioration in tensile properties, correlated with the amount of starch present in the blends (neat PHBV < 30% starch < 50% starch). Incorporation of PEO into starch-PHBV blends had little or no effect on the rate of weight loss. Starch in blends degraded faster than PHBV and it accelerated PHBV degradation. Also, PHBV did not retard starch degradation. After 125 days of exposure to compost, neat PHBV lost 7% of its weight (0.056% weight loss/day), while the PHBV component of a 50% starch blend lost 41% of its weight (0.328% weight loss/day). PHB and PHV moieties within the copolymer degraded at similar rates, regardless of the presence of starch, as determined by ¹H-NMR spectroscopy. GPC analyses revealed that, while the number average molecular weight (Mn) of PHBV in all exposed samples decreased, there was no significant difference in this decrease between neat PHBV as opposed to PHBV blended with starch. SEM showed homogeneously distributed starch granules embedded in a PHBV matrix, typical of a filler material. Starch granules were rapidly depleted during exposure to compost, increasing the surface area of the PHBV matrix.     

Historical Weathering Based on Chemical Analyses of Two Spodosols in Southern Sweden

Chemical weathering losses were calculated for two conifer stands in relation to ongoing studies on liming effects and ash amendments on chemical status, soil solution chemistry and soil genesis. Weathering losses were based on elemental depletion trends in soil profiles since deglaciation and exposure to the weathering environment. Gradients in total geochemical composition were assumed to reflect alteration over time. Study sites were Horröd and Hasslöv in southern Sweden. Both Horröd and Hasslöv sites are located on sandy loamy Weichselian till at an altitude of 85 and 190 m a.s.l., respectively. Aliquots from volume determined samples from a number of soil levels were fused with lithium metaborate, dissolved in HNO₃, and analysed by ICP – AES. Results indicated highest cumulative weathering losses at Hasslöv. The weathering losses for the elements are in the following order:Si > Al > K > Na > Ca > MgTotal annual losses for Ca+Mg+K+Na, expressed in mmol_c m^-2 yr^-1, amounted to c. 28 and 58 at Horröd and Hasslöv, respectively. Variations between study sites could not be explained by differences in bulk density, geochemistry or mineralogy. The accumulated weathering losses since deglaciation were larger in the uppermost 15 cm than in deeper B horizons for most elements studied.