粉煤灰中游离氧化钙的分布特性

本文探讨了粉煤灰中游离氧化钙的含量与颗粒大小的关系。对9个电厂23个灰样测定的结果表明:游离氧化钙的含量一般随颗粒粒径减小而增大;50μm 以下的细颗粒富集了大约70%的游离氧化钙。此种分布特性与电除尘器分电场序数无关。     

半干法脱除球团烟气中的SO2及Hg0

采用钙基吸收剂及复合氧化剂半干法脱除模拟球团烟气中的SO_2及Hg~0,考察了多因素条件对吸收效果的影响。实验结果表明,在以NaClO和NaClO_2为复合氧化剂、 NaClO与NaClO_2体积比1∶0.5、复合氧化剂质量分数3%、反应温度110℃、钙基吸收剂质量3.0 g、模拟烟气进气流量1.2 L/min的条件下,SO_2和Hg~0的脱除率分别为98%和93%,证明钙基吸收剂与复合氧化剂对污染物球团烟气中的SO_2和Hg~0有良好的脱除作用。     

某燃煤电厂锅炉除尘器“电改袋”后问题的数值模拟分析

针对某燃煤电厂除尘器“电改袋”后运行中出现的设备阻力较高、滤袋破损、收尘灰斗灰量不均匀问题进行分析.采用数值模拟分析方法对除尘器内部的气流组织进行模拟试验研究,结合现场实际设备建立了物理模型,对除尘空间颗粒物沉积进行了理论分析,结果表明进入除尘器的颗粒物(200 μm以下)沉降速度低于1.5 m/s.把含尘气体近似为气相气流,采用Realizable κ-ε紊流模型进行该袋式除尘器除尘空间流场计算,结果表明除尘区中间气流平均上升速度达到1.0 m/s,在该上升气流作用下大部分颗粒物难以自然沉积是造成阻力增大的主要原因之一；采用长流程设计除尘空间会造成袋底下部空间的气流速度较大,前大后小,平均相差达到4倍左右,造成滤袋收尘量后移,它是造成滤袋破损和阻力升高的主要原因；各仓室流量分配相差11％～13％及各仓室滤袋流量分配不均容易造成局部滤袋破损几率增高.     

袋式除尘器在国电九江电厂的应用及其对PM2.5的脱除分析

国电九江发电厂“上大压小”扩建工程2 x 660 MW超超临界燃煤机组配套采用旋转式低压脉冲袋式除尘器，对袋式除尘器进出口烟气中PM2.5、SO2、NO、SO3、氯化物、汞等浓度进行了现场测试，结果表明，该袋式除尘器能有效脱除烟气中的PM2.5，其PM2.5数浓度和质量浓度脱除效率可分别高达98.9%和99.7%，同时还可脱除富集在PM2.5表面的颗粒态汞。     

CeO2/TiO2纳米管催化剂脱硝性能研究

利用废气中本身含有的CO催化还原烟气中的NO_x,可以实现以废治废。采用TiO₂纳米管负载CeO₂,制备CeO₂/TiO₂纳米管催化剂,并对其进行了SEM表征及影响因素实验。实验结果表明：在n（Ce）∶n（Ti）=3∶7、焙烧温度500 ℃、焙烧时间3 h时制备的CeO₂/TiO₂纳米管催化剂形貌较好,表面颗粒分布相对均匀;反应温度400~600 ℃时NO脱除率达98%;该催化剂具有一定的抗氧性能;当n（SO₂）∶n（NO）=（1∶2）~（2∶1）时,NO脱除率仍然在95%以上。     

固定床活性炭干法烟气脱硫过程的模拟研究

采用流程模拟软件对固定床活性炭干法烟气脱硫过程进行模拟,并用已公开发表的文献实验数据进行了模型验证。模型验证结果与文献值吻合较好。利用该模型对活性炭干法烟气脱硫过程进行模拟研究,探讨了脱硫过程中床层高度、进口烟气中SO_2质量浓度、吸附温度等工艺参数对SO_2脱除率的影响。模拟结果表明:随床层高度增加,SO_2脱除率提高;随进口烟气中SO_2质量浓度增加,SO_2脱除率提高;在吸附温度为100~160℃的范围内,随吸附温度升高,SO_2脱除率逐渐下降。     

混合表面活性剂-浊点萃取法测定沉积物中多环芳烃的含量

以混合型表面活性剂（十二烷基硫酸钠（SDS）和对叔辛基苯基聚己二醇醚（Triton X-114））为萃取剂，采用浊点萃取法萃取沉积物中的15种多环芳烃（PAHs），并利用HPLC技术测定15种PAHs的含量。实验结果表明，当混合型表面活性剂的加入量 3％（w）、混合型表面活性剂中SDS含量 50%（φ）、Na2SO4含量 8％（w）、萃取温度 60 ℃、超声萃取时间 10 min 时，15种PAHs的线性关系良好，r=0.998 9~0.999 7，检出限0.4~8.2 μg/L，加标回收率71.22%~97.36%，相对标准偏差0.92%~4.36%（n=6）。     

烟气组分对低温等离子体协同TiO_2光催化工艺氧化Hg~0的影响

采用介质阻挡放电低温等离子体协同TiO2光催化工艺氧化烟气中Hg0,考察了烟气组分对氧化效果的影响。实验结果表明:低温等离子体放电会产生大量近紫外光;在6 k V电压下,低温等离子体协同TiO2光催化工艺时N2/Hg0氛围下Hg0的氧化率达86%,显著高于单一等离子体时的30%;O2和H2O产生的活性粒子会使Hg0氧化率进一步提高,在5 k V电压下,N2/Hg0氛围中添加5%(φ)O2或5%(φ)H2O,低温等离子体协同TiO2光催化工艺时可分别获得96%和94%的氧化率;NO与Hg0的竞争关系会导致作用于Hg0的活性粒子减少,抑制低温等离子体对Hg0的氧化,而在低温等离子体协同TiO2光催化时,抑制作用减弱;在复杂烟气氛围下,低温等离子体协同TiO2光催化对Hg0仍保持了较高的氧化率,3次重复实验的Hg0氧化率均接近92%。     

尘粒分散度的数据处理及绘图程序

分析粉尘颗粒样品的分散度对于选择除尘器、评价除尘器的特性以及评价烟气粉尘排放对大气污染的影响极为重要。粉尘粒径分散度反应了粉尘颗粒大小的分布频率,其表示方法可呈正态分布、对数正态分布、罗氏(Rosin and Rammer)分布等。通常在使用仪器(如显微镜、筛分、气相冲击仪、巴柯离心仪、库尔特计数器等)测得粉尘样品的一组分散度数据后,需要进行数据     

有机溶剂浸取石油污染土壤中的多环芳烃

采用索氏提取法和气相色谱分析了某炼油厂周边土壤中的多环芳烃的种类及含量,考察了6种有机溶剂对土壤中多环芳烃的浸取效果,探讨了溶剂与溶质溶解度参数差异对浸取效果的影响。结果表明：土壤试样中含有蒽、荧蒽、芘、 、苯并[a]蒽、苯并[b]荧蒽、苯并[k]荧蒽和苯并[a]芘8种多环芳烃,其含量分别为4.20,22.05,10.62,4.26,5.54,0.80,0.94,4.18 mg/kg;筛选出二氯甲烷作为土壤中多环芳烃的浸取溶剂;最佳浸取条件为浸取时间10 min、浸取温度30 ℃、溶剂与土壤的液固比5:1（mL/g）、土壤含水量8%,在此条件下,总多环芳烃浸出率为83.0%,各种多环芳烃的浸出率分别为蒽97.8%、荧蒽78.2%、芘99.9%、 98.5%、苯并[a]蒽81.1%、苯并[b]荧蒽47.6%、苯并[k]荧蒽14.8%、苯并[a]芘58.7%。     

Programs assessing implementation and effectiveness of state forest practice rules and BMPs in the West

The major forest nonpoint source control programs in the West are largely regulatory, either under forest practices acts (California, Idaho, New Mexico, Nevada, Oregon, and Washington) or a streamside management act (Montana). These programs and the specific rules they enforce continue to undergo intensive scrutiny. Still, the questions are the same for these regulatory programs as for states that base nonpoint source control on voluntary BMPs (Arizona, Colorado, Utah, Wyoming). Are the rules or BMPs being applied, and are they effective in reducing nonpoint source pollution to levels that protect beneficial uses of water? The level of debate about forestry in the West has resulted in detailed monitoring and research to answer these questions. In the past, state agencies have assumed levels of BMP compliance based on the percent of operations without enforcement actions. These estimates are being replaced by statistically valid and reproducible monitoring of forest practices rules and BMP compliance levels. BMP effectiveness is being assessed using both qualitative and quantitative methods. This can involve field assessments, process-based research, and control watershed studies. Some trend monitoring is also beginning. With the regional implementation rate for forestry BMPs at about 94% and rising, it is likely that effectiveness testing will continue to be a priority and consume the majority of assessment resources for this region.     

Hysteresis in Reversal of Central European Mountain Lakes from Atmospheric Acidification

Extremely high emissions of S and N compounds in Central Europe (both 280 mmol m^-2 yr^-1) declined by 70and 35%, respectively, during the last decade. Decreaseddeposition rates of SO₄ ^-2, NO₃ ^-, and NH₄ ⁺ in the region paralleled emission declines. The reduction in atmospheric inputs of S and N to mountain ecosystemshas resulted in a pronounced reversal of acidification in the Tatra Mountains and Bohemian Forest lakes. Between the 1987–1990and 1997–1999 periods, concentrations of SO₄ ^-2 and NO₃ ^- decreased (average ± standard deviation) by 22±7 and 12±7 mol L^-1, respectively, in theTatra Mountains, and by 19±7 and 15±10 mol L^-1, respectively, in the Bohemian Forest. Their decrease was compensated in part (1) by a decrease in Ca²⁺ + Mg²⁺ (17±7 mol L^-1) and H⁺ (4±6 mol L^-1), and an increase in HCO₃ ^-(10±10 mol L^-1) in the Tatra Mountains lakes, and (2) by a decrease in Al (7±4 mol L^-1), Ca²⁺ + Mg²⁺ (9±6 mol L^-1), and H⁺ (6±5 mol L^-1), in Bohemian Forest lakes. Despite the rapid decline in lake water concentrations of SO₄ ^-2 and NO₃ ^- in response to reduced S and N emissions, their present concentrations in some lakes are higher than predictionsbased on observed concentrations at comparable emission rates during development of acidification. This hysteresis in chemical reversal from acidification has delayed biological recovery of the lakes. The only unequivocal sign of biological recovery hasbeen observed in erné Lake (Bohemian Forest) where a cladoceran species Ceriodaphnia quadrangular has recentlyreached its pre-acidification abundance.     

Reconstruction of Long-Term Changes in Lake water Chemistry,Zooplankton and Benthos of a Small,Acidified High-Mountain Lake: Magic Modelling and Palaeolimnogical Analysis

Starolesnianske pleso is a small and shallow acid lake in the High Tatra Mountains, situated at 2000 m above sea level, on granitic bedrock, with sparse and thin soil cover. When detailed measurements began in the 1980s Starolesnianske pleso had pH below 5 and only one species of cladoceran zooplankton, the ubiquitous Chydorus sphaericusPalaeolimnological investigations show changes in cladoceran zooplankton and chironomid zoobenthic assemblages since about 1920 and a major change in 1970–1980. The dynamic acidification model MAGIC was used to reconstruct changes in water chemistry over the past 150 years. The results from MAGIC agree well with the sediment record; pH levels gradually decreased from 6.5 in the mid-1800s to about 5.6 in 1920 (first response in biota) to below 5.0 by 1970, and concentrations of inorganic aluminium rose dramatically beginning about 1960. In the 1990s the lake water chemistry showed clear signs of reversal in acidification brought about by a major decline in S deposition.     

Heavy Metals Removal by Biosorption and Flotation

The removal of a mixture of heavy (toxic) metal cations (copper, nickeland zinc) from liquid effluents was investigated in this study at pilotscale, using counter-current contact mode. The innovative processinvolved the abstraction of metal ions onto fungal biosorbents, followedby the application of flotation for the subsequent solid/liquid separationof biomass particles. The ability of microorganisms to remove metal ionsfrom aqueous solutions is a well-known phenomenon. Nevertheless,engineering considerations are very important in decisions, concerningthe commercial future of biosorption and practical solutions are neededfor certain problems, such as the efficient post-separation ofmetal-loaded biomass. The two processes (flotation and biosorption) caneffectively operate in combination, in what it was termed biosorptiveflotation process. The sorbents may be recycled, after appropriate elutionof metals, as well as the treated (clean) water.     

Selection of Autochthonous Plant Species from SE Spain for Soil Lead Phytoremediation Purposes

Mining activity in SE of Spain, in the west Mediterranean coast, originated more than two millenniums ago. It has generated huge areas affected by heavy metals contamination, especially of lead, which is possibly one of the most important. Investigations related to the selection of autochthonous plant taxa from a typical Spanish Mediterranean area, useful for phytoextraction and phytostabilization purposes in these polluted areas are shown. Under these edaphoclimatic conditions 12 interesting species were considered, from them six taxa were chosen for further studies. Some plant species have been proposed either for phytoextraction or phytostabilization purposes. Recommendations for further research have been discussed.     

Concentrations and Pools of Heavy Metals in Urban Soils in Stockholm,Sweden

The concentrations of heavy metals (Cd, Cr, Cu, Hg, Ni, Pb andZn) and arsenic (As) were surveyed and the metal pools estimatedin soils in Stockholm Municipality. The sampling sites were distributed all over the entire municipality with a higher sampling density in the city centre. Soils were sampled to a maximum depth of 25 to 60 cm. Soil texture, total-C content, electrical conductivity and pH were analysed. Heavy metal concentrations were determined after wet digestion with boiling7 M HNO₃.The results showed a wide range in heavy metal concentrations, as well as in other soil properties. The city centre soils constituted a rather homogeneous group whereas outside this areano geographical zones could be distinguished. These soils were grouped based on present land use, i.e. undisturbed soils, public parks, wasteland (mainly former industrial areas), and roadside soils. The city centre and wasteland soils generally hadenhanced heavy metal concentrations to at least 30 cm depth compared to park soils outside the city centre and rural (arable)soils in the region, which were used to estimate background levels. For example, the mean Hg concentration was 0.9 (max 3.3)mg kg^-1 soil at 0–5 cm and 1.0 (max 2.9) at 30 cm depth in the city centre soils, while the background level was 0,04 mg kg^-1. Corresponding values for Pb were 104 (max 444) and135 (max 339) mg kg^-1, at 0–5 and 30 cm, respectively, while the background level was 17 mg kg^-1.The average soil pools (0–30 cm depth) of Cu, Pb and Zn were 21,38 and 58 g m^-2 respectively, which for Pb was 3–4 timeshigher and for Cu and Zn 1.5–2 times higher than the backgroundlevel. The total amount of accumulated metals (down to 30 cm)in the city centre soils (4.5^*10 ⁶ m² public gardens and green areas) was estimated at 80, 1.1, 120 and 40 t for Cu, Hg, Pb and Zn, respectively. The study showed (1) thatfrom a metal contamination point of view, more homogeneous soilgroups were obtained based on present land use than on geographicdistance to the city centre, (2) the importance of establishing a background level in order to quantify the degree of contamination, and (3) soil samples has to be taken below the surface layer (and deeper than 30 cm) in order to quantify theaccumulated metal pools in urban soils.     

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.     

我国电子废物回收处理产业政策及机遇与挑战分析

针对近年我国频繁出台的电子废物回收处理产业政策,系统论述了其发展脉络,并从循环经济角度出发,分析了我国电子废物产业发展的主体思路,同时还对我国电子废物回收处理产业发展机遇与存在的问题进行剖析,对如何稳定企业的电子废物来源、提升产业技术水平及降低企业运营成本进行建议性分析。     

Effect of Coconut, Sisal and Jute Fibers on the Properties of Starch/Gluten/Glycerol Matrix

Coconut, sisal and jute fibers were added as reinforcement materials in a biodegradable polymer matrix comprised of starch/gluten/glycerol. The content of fibers used in the composites varied from 5% to 30% by weight of the total polymers (starch and gluten). Materials were processed in a Haake torque rheometer (120 °C, 50 rpm) for 6 min. The mixtures obtained were molded by heat compression and further characterized. Addition of lignocellulosic fibers in the matrix decreased the water absorption at equilibrium. The diffusion coefficient decreased sharply around 5% fiber concentration, and further fiber additions caused only small variations. The thermogravimetric (TG) analysis revealed improved thermal stability of matrix upon addition of fibers. The Young’s modulus and ultimate tensile strength increased with fiber content in the matrix. The storage modulus increased with increasing fiber content, whereas tanδ curves decreased, confirming the reinforcing effect of the fibers. Morphology of the composites analyzed under the scanning electron microscope (SEM) exhibited good interfacial adhesion between the matrix and the added fibers. Matrix degraded rapidly in compost, and addition of increased amounts of coconut fiber in the matrix caused a slowdown the biodegradability of the matrix. Names are necessary to report factually on available data; however, the USDA neither guarantees nor warrants the standard of the product, and the use of the name by USDA implies no approval of the product to the exclusion of others that may be suitable.     

Nitrous oxide emission from some English and Welsh rivers and estuaries

Nutrient and N₂O concentrations in the water columns were measured seasonally over a full salinity range in the nutrified rivers Colne, Stour, Orwell, Deben, Trent, Ouse and Humber and their estuaries on the east coast of England between August 2001 and May 2002, and in the oligotrophic rivers Conwy, Dovey and Mawddach in North and West Wales between August 2002 and May 2003. Nutrient and N₂O concentrations in the nutrified English rivers and estuaries were much higher than those in the Welsh rivers. N₂O concentrations and % saturation in the estuaries were significantly correlated with nitrate, nitrite and ammonium concentrations in the water. The strongest correlation was with nitrite (r² = 0.56, p < 0.01), suggesting that nitrite was the most significant factor among the different nutrients in regulating N₂O concentration in the estuaries. N₂O concentrations in the English rivers and estuaries were supersaturated throughout the year with annual averages from 186.9 to 992.9%, indicating that these rivers and estuaries were sources of atmospheric N₂O, whereas in the Welsh rivers N₂O concentrations were much lower with annual averages from 113.6 to 137.4% saturation. Although the estuarine area in the Colne was almost the same as that in the Conwy, the annual N₂O emission from the Colne was much higher (937498 mol N yr^–1) than in the Conwy (23020 mol N yr^–1). On the east coast, riverine emissions of N₂O were only 0.5–12.5% of the total emission from rivers and estuaries. Thus rivers were negligible, but estuaries were significant contributors to the UK N₂O inventory.