高效喷淋泡沫脱硫技术及装置的应用

SO2是产生酸雨的主要气体,其主要来源于工业燃煤锅炉.以沈阳一家电厂为例,该厂选用新型高效的喷淋泡沫脱硫除尘器对锅炉排放的SO2进行治理.进入喷淋泡沫塔前的SO2平均浓度为2780 mg/m3,经脱硫后出塔平均浓度为289.3 mg/m3,去除率为89.6%.结果表明,这种有别于传统湿法的新型高效的喷淋泡沫脱硫技术及装置具有脱硫效率高、装置占地少、运行稳定、沉淀物易于回收利用等特点,对锅炉排放的SO2进行治理是非常有效的.     

湿法脱硫石灰石浆液密度的敏感性分析

石灰石浆液的性能是影响湿法烟气脱硫效率的主要因素,而石灰石浆液的密度又是影响其性能的主要参数。现场制浆过程中,运行参数的变动会使得浆液密度值发生变化,从而影响浆液性能。因此,通过调整制浆系统运行参数,寻找石灰石浆液密度敏感因素,对优化浆液性能具有重要意义。以某600 MW火力发电厂湿式脱硫制浆系统作为研究对象,通过现场...     

湿法烟气脱硫系统的脱汞性能现场实验

分析湿法烟气脱硫系统的脱汞性能,对控制燃煤电厂的汞污染具有重要意义。利用安大略水法和吸附管法分别对某600 MW电厂湿法脱硫系统的进出口的烟气进行了采样,测量了烟气中各形态汞浓度,并分析了该系统对烟气总汞、气态氧化态汞的脱除效果以及对气态单质汞的影响。研究结果表明,安大略水法和吸附管法均能较为准确地测定湿法脱硫系统进出口烟气中的汞含量,测得入口和出口的氧化汞与平均值的相对误差的绝对值分别为3.5%和1.3%;入口和出口的单质汞与平均值相对误差的绝对值分别为16.6%和3.3%。其中吸附管法操作相对简单。通过湿法烟气脱硫系统后,烟气中氧化态汞的浓度可下降87.5%,其中约67.5%的氧化态汞被湿法脱硫系统脱除,约20%的氧化态汞在脱硫浆液的还原作用下被还原为单质汞,导致脱硫系统出口的单质汞浓度高于入口。     

蛋壳、贝壳实现层烧炉脱硫脱硝

在4.2MW链条锅炉使用蛋壳、贝壳粉平铺在煤层上部进行炉内脱硫脱硝后,通过风机的负压携带将燃烧形成的CaO随烟气带入湿法除尘设备,完成与NaOH的双碱法脱硫脱硝。结果表明,脱硫效率80%,脱硝效率50%。烟气排放指标优于国标。风机携带的CaO对水冷壁形成清扫作用,运行130d节约煤炭20%。     

石灰和石灰石湿法脱硫系统运行控制指标探讨

钙基脱硫剂湿式脱硫系统是目前市场上广泛采用的烟气脱硫系统。文章分析了石灰和石灰石自身不同的物理化学特性对湿法脱硫系统运行控制指标的影响,得出了对于采用石灰和石灰石作为脱硫剂的湿式脱硫系统的最佳pH为8．0和5．8～6．2,脱硫浆液流量与烟气流量之比为10．0和5．6,钙硫比(化学过量比)为1．05～1．15和1．25～1．60。     

中、日、美三国烟气脱硫技术的发展和现状

本文详细介绍了日本、美国和中国烟气脱硫的现状和发展趋势。着重综述了燃煤发电厂的脱硫技术、装置、投资、操作费用、能耗、副产物的处理和操作经验等。 日本是世界上控制SO_2最有成效的国家,电厂烟气脱硫方法中湿法石灰石(石灰)——石膏法占了多数,当然也是付出了巨大经济代价的。 美国燃煤发电占了50％,因此,SO_2排放源主要来自燃煤电厂,SO_2控制主要采用湿法,一些地区内SO_2污染得到了控制。 中国的能源是以煤炭为主,每年SO_2排放量达到1600万吨,形成酸雨危害,目前正在采取控制技术措施,研究减少SO_2排放的方法和策略。     

半干半湿法烟气脱硫装置中喷雾增湿技术的研究

脱硫塔内喷雾增湿技术是影响燃煤锅炉半干半湿法烟气脱硫效果的一个重要环节。分析了供水量和压力的变化关系 ,通过对脱硫装置喷雾增湿技术的优化 ,实现对增湿系统高压水的压强的精确调节 ,控制脱硫塔内雾滴的颗粒直径在 80 μm左右 ,从而达到理想的增湿效果     

燃煤锅炉烟气除尘系统改造

烷基苯厂锅炉烟气除尘系统改造选用文丘里麻石水膜除尘器,除尘脱硫废水与碱性冲渣水中和、过滤后再循环泵提升至冲渣系统,实现燃煤锅炉除尘脱硫废水循环利用。改造后的除尘系统运行情况良好,锅炉的烟尘排放浓度及烟气黑度均达到了国家现行三类区排放标准,二氧化硫排放浓度低于国家允许排放标准。     

双循环多级水幕脱硫塔的设计和性能测试

双循环多级水幕脱硫塔是在常规两段式湿法脱硫塔基础上加以改进而成的新型脱硫塔,其双循环浆液采用不同pH控制,低pH促进CaCO2溶解,高pH提高SO2吸收效果;同时,多级水幕强化气液流态,增加气液接触面积和传质动力,促进对SO2的吸收.实验利用SPSSV13.0软件进行正交实验设计,通过数据分析得出两个不同的优化运行方案,再利用多指标分析法中的综合平衡法进行单因素实验,得出最优运行方案.在最优运行方案条件下,即烟气流量为100 m3/h,上循环浆液pH为6.0,下循环浆液pH为4.8,上、下循环液气比均为20 L/m3,人口 SO2质量浓度为1 000mg/m3时,脱硫效率达97.8%,CaCO3利用率为95.2%,钙硫质量比约为1.03.双循环多级水幕脱硫塔具有良好的应用前景,实验结果对现场脱硫系统的调试和运行有很好的参考价值.     

基于多源数据融合的浙江省温室气体与大气污染物排放协同研究

减污降碳协同是中国新发展阶段经济社会发展全面绿色转型的必然选择。以浙江省为研究对象,应用多源数据融合方法构建1 km×1 km的温室气体与大气污染物排放网格,采用耦合协调模型识别温室气体和大气污染物排放的协同高值区、磨合区、拮抗区等。研究结果显示,占浙江省国土空间0.68%的协同高值区集聚了30.6%的温室气体排放和38.3%的大气污染物排放,根据不同区域协同排放特性提出减污降碳治理的空间管控优先次序建议、重点行业治理建议、重点因子治理建议等,丰富了区域减污降碳协同的精细化定量分析方法和中长期治理路径优化技术方法。     

Meta-analysis of time-series studies of air pollution and mortality: effects of gases and particles and the influence of cause of death,age, and season

A comprehensive, systematic synthesis was conducted of daily time-series studies of air pollution and mortality from around the world. Estimates of effect sizes were extracted from 109 studies, from single- and multipollutant models, and by cause of death, age, and season. Random effects pooled estimates of excess all-cause mortality (single-pollutant models) associated with a change in pollutant concentration equal to the mean value among a representative group of cities were 2.0% (95% CI 1.5-2.4%) per 31.3 microg/m3 particulate matter (PM) of median diameter < or = 10 microm (PM10); 1.7% (1.2-2.2%) per 1.1 ppm CO; 2.8% (2.1-3.5%) per 24.0 ppb NO2; 1.6% (1.1-2.0%) per 31.2 ppb O3; and 0.9% (0.7-1.2%) per 9.4 ppb SO2 (daily maximum concentration for O3, daily average for others). Effect sizes were generally reduced in multipollutant models, but remained significantly different from zero for PM10 and SO2. Larger effect sizes were observed for respiratory mortality for all pollutants except O3. Heterogeneity among studies was partially accounted for by differences in variability of pollutant concentrations, and results were robust to alternative approaches to selecting estimates from the pool of available candidates. This synthesis leaves little doubt that acute air pollution exposure is a significant contributor to mortality.     

Sources and fate of PCDD and PCDF

PCDD and PCDF were found in urban air particulates from St. Louis and Washington, D.C., and in sediments from the Great Lakes and Siskiwit Lake, Isle Royale. The similarity between the PCDD and PCDF found in air particulates and sediment samples and the presence of PCDD and PCDF in sediment from Siskiwit Lake (a location which can receive only atmospheric inputs) suggest that these compounds are emitted to the atmosphere from combustion sources. The historical input of PCDD and PCDF to dated sediment cores shows a strong increase since 1940, and this suggests that the incineration of chlorinated organic compounds is an important source of PCDD and PCDF to the environment.     

Field and laboratory studies of the fate and enantiomeric enrichment of venlafaxine and O-desmethylvenlafaxine under aerobic and anaerobic conditions

The stereoselectivity of R,S-venlafaxine and its metabolites R,S-O-desmethylvenlafaxine, N-desmethylvenlafaxine, O,N-didesmethylvenlafaxine, N,N-didesmethylvenlafaxine and tridesmethylvenlafaxine was studied in three processes: (i) anaerobic and aerobic laboratory scale tests; (ii) six wastewater treatment plants (WWTPs) operating under different conditions; and (iii) a variety of wastewater treatments including conventional activated sludge, natural attenuation along a receiving river stream and storage in operational and seasonal reservoirs. In the laboratory and field studies, the degradation of the venlafaxine yielded O-desmethylvenalfaxine as the dominant metabolite under aerobic and anaerobic conditions. Venlafaxine was almost exclusively converted to O-desmethylvenlafaxine under anaerobic conditions, but only a fraction of the drug was transformed to O-desmethylvenlafaxine under aerobic conditions. Degradation of venlafaxine involved only small stereoisomeric selectivity. In contrast, the degradation of O-desmethylvenlafaxine yielded remarkable S to R enrichment under aerobic conditions but none under anaerobic conditions. Determination of venlafaxine and its metabolites in the WWTPs agreed well with the stereoselectivity observed in the laboratory studies. Our results suggest that the levels of the drug and its metabolites and the stereoisomeric enrichment of the metabolite and its parent drug can be used for source tracking and for discrimination between domestic and nondomestic wastewater pollution. This was indeed demonstrated in the investigations carried out at the Jerusalem WWTP.     

Meta-Analysis of Time-Series Studies of Air Pollution and Mortality: Effects of Gases and Particles and the Influence of Cause of Death,Age, and Season

Abstract

A comprehensive, systematic synthesis was conducted of daily time-series studies of air pollution and mortality from around the world. Estimates of effect sizes were extracted from 109 studies, from single- and multipollutant models, and by cause of death, age, and season. Random effects pooled estimates of excess all-cause mortality (single-pollutant models) associated with a change in pollutant concentration equal to the mean value among a representative group of cities were 2.0% (95% CI 1.5-2.4%) per 31.3 μg/m³ particulate matter (PM) of median diameter <10 μm (PM₁₀); 1.7% (1.2-2.2%) per 1.1 ppm CO; 2.8% (2.1-3.5%) per 24.0 ppb NO₂; 1.6% (1.1-2.0%) per 31.2 ppb O₃; and 0.9% (0.7-1.2%) per 9.4 ppb SO₂ (daily maximum concentration for O₃, daily average for others). Effect sizes were generally reduced in multipollutant models, but remained significantly different from zero for PM₁₀ and SO₂. Larger effect sizes were observed for respiratory mortality for all pollutants except O₃. Heterogeneity among studies was partially accounted for by differences in variability of pollutant concentrations, and results were robust to alternative approaches to selecting estimates from the pool of available candidates. This synthesis leaves little doubt that acute air pollution exposure is a significant contributor to mortality.     

Sorption and desorption of Cu and Cd by macroalgae and microalgae

The sorption and desorption of Cu and Cd by two species of brown macroalgae and five species of microalgae were studied. The two brown macroalgae, Laminaria japonica and Sargassum kjellmanianum, were found to have high capacities at pHs between 4.0 and 5.0 while for microalgae, optimum pH lay at 6.7. The presence of other cations in solution was found to reduce the sorption of the target cation, suggesting a competition for sorption sites on organisms. Sorption isotherms obeyed the Freundlich equation, suggesting involvement of a multiplicity of mechanisms and sorption sites. For the microalgae tested, Spirulina platensis had the highest capacity for Cd, followed by Nannochloropsis oculata, Phaeodactylum tricornutum, Platymonas cordifolia and Chaetoceros minutissimus. The reversibility of metal sorption by macroalgae was examined and the results show that both HCl and EDTA solutions were very effective in desorbing sorbed metal ions from macroalgae, with up to 99.5% of metals being recovered. The regenerated biomass showed undiminished sorption performance for the two metals studied, suggesting the potential of such material for use in water and wastewater treatment.     

骆马湖富营养化和生态状况调查与评价

为了了解骆马湖水质状况，在2005年对骆马湖富营养化状态和生态特性进行了调查，并结合“十五”期间的监测资料进行了分析。2005年骆马湖水体中总氮和总磷的平均值超《地表水环境质量标准》（GB3838-2002）中Ⅲ类，超标情况分别为0．78倍和0．54倍，达到湖库特定项目Ⅳ类水标准，骆马湖处于轻度富营养化状态。对骆马湖生态特征分析表明，由于该湖泊的形态以及“藻型浊水状态”和“泥沙型浊水状态”交替出现，遏制了湖水从高营养盐含量向全面富营养化状态演变，保障了底栖动物的良好生长环境，从而形成了骆马湖独特的环境生态平衡。     

剩余污泥浓缩脱水投药量优化和模型建立

应用高分子阳离子絮凝剂（CPF-100）和聚丙烯酰胺（PAM）对污水厂剩余污泥进行浓缩脱水实验，研究表明：CPF-100的浓缩脱水效果优于PAM；当CPF-00投加量为1．16‰时，污泥沉降性能改善程度为37．51％；且在CPF-100投加量逐渐增大的初始阶段，污泥沉降性能改善程度随投加量的增加而增大，但CPF-100投加量也不宜过大，当CPF-100投加量超过1．16‰后，反而会使浓缩脱水效果变差。同时，建立了污泥沉降性能改善程度与絮凝剂CPF-100投加量、沉降时间之间的数学模型，其能较好地反映污水厂剩余污泥的浓缩脱水效果。     

Copper-catalyzed chlorination and condensation of acetylene and dichloroacetylene

The chlorination and condensation of acetylene at low temperatures is demonstrated using copper chlorides as chlorinated agents coated to model borosilicate surfaces. Experiments with and without both a chlorine source and borosilicate surfaces indicate the absence of gas-phase and gas-surface reactions. Chlorination and condensation occur only in the presence of the copper catalyst. C₂ through C₈ organic products were observed in the effluent; PCDD/F were only observed from extraction of the borosilicate surfaces. A global reaction model is proposed that is consistent with the observed product distributions. Similar experiments with dichloroacetylene indicate greater reactivity in the absence of the copper catalyst. Reaction is observed in the gas-phase and in the presence of borosilicate surfaces at low temperatures. The formation of hexachlorobenzene is only observed in the presence of a copper catalyst. PCDD/F were only observed from extraction of the borosilicate surfaces. A global reaction model is proposed for the formation of hexachlorobenzene from dichloroacetylene.     

Aerobic and anaerobic degradation of profluralin and trifluralin

Abstract

The degradation of profluralin [N‐(cyclopropylmethyl)‐α,α,α‐trifluoro‐2,6‐dinitro‐N‐propyl‐]p‐toluidine] and trifluralin (α,α,α‐trifluoro‐2,6‐dinitro‐N,N‐dipropyl‐p‐toluidine) was studied under aerobic and anaerobic soil conditions. Three soils (Goldsboro loamy sand, Cecil loamy sand, Drummer clay loam) were each treated with 1 ppmw herbicide; anaerobic conditions were maintained by flooding. Soil samples were extracted monthly and subjected to TLC analysis. No degradation was detected in sterile controls. Aerobic degradation of both herbicides was greatest in the Cecil loamy sand soil over the entire incubation period. Degradation of profluralin in Cecil soil under aerobic conditions was 86 percent after 4 months with three products detected; 83 percent of the trifluralin was degraded with two products detected. Anaerobic degradation accounted for 72 percent of the profluralin and 78 percent of the trifluralin after 4 months. Degradation of both herbicides increased with incubation time for the first 3 months and decreased slightly thereafter. Generally there was more extensive degradation (percent and in number of products formed) of profluralin than trifluralin under the conditions tested. More degradation products were detected for both herbicides under aerobic conditions than under anaerobic conditions.