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一般可通过水泥固化生活垃圾焚烧飞灰中重金属,但不同标号水泥的固化效果与经济效益不同。研究了3种标号(325、425、525)的普通硅酸盐水泥在不同用量(30%、40%)下对飞灰中重金属的固化作用。结果表明,飞灰中5种特征重金属Cr、Zn、Cd、Pb、Ni中仅有Pb和Ni的浸出质量浓度超过《生活垃圾填埋场污染控制标准》,水泥添加量为30%时,3种标号325、425、525的固化块中Pb的浸出质量浓度分别为46.266、61.122、67.423μg·L-1,相较于40%添加量为80.315、31.791、25.392μg·L-1,其浸出结果差异较小,Ni的浸出结果与Pb类似。分析重金属化学形态发现,随着水泥标号的上升,Pb和Ni的残渣态百分比呈上升趋势。对比固化块的XRD结果、电镜图像、孔隙结构和累计孔隙度发现,随着水泥标号上升固化块结构更密实,飞灰中的重金属固化效果更好,但3种标号的水泥对飞灰的固化效果差异较小。因此,掺加30%的325水泥即可较好地固化垃圾焚烧飞灰。本研究结果可为控制填埋场中飞灰固化块的浸出浓度提供参考。 相似文献
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城市生活垃圾焚烧飞灰的熔融分离处理 总被引:1,自引:1,他引:0
焚烧法处理城市生活垃圾已在世界先进发达国家广泛采用。垃圾焚烧飞灰含有大量的重金属,必须进行合理安全处置。在分析城市生活垃圾焚烧飞灰的物理化学性质基础上,研究了垃圾焚烧飞灰固化成型、熔融分离的无害化处理新工艺。实验结果表明:飞灰固化成球的适宜粘结剂为5%~7%消石灰,养护时间为10~12 d,固化球强度达0.24 kg/cm2以上,可以满足运输和熔化分离要求;固化后的飞灰在1 300℃左右熔融分离后,重金属的分离效果好,达到97%以上,可达到无害化处理标准;对1 300℃和1 400℃熔融分离后熔渣的重金属浸出毒性测试显示,重金属浸出毒性问题可以完全解除。研究结果表明,采用飞灰固化-熔融分离工艺处理城市生活垃圾焚烧飞灰是可行的。 相似文献
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采用有机硫稳定剂(DTCR)与水泥对城市垃圾焚烧飞灰进行稳定/固化处理,研究了飞灰中Cd、Pb、Zn的浸出毒性和固化体的抗压强度,比较了螯合稳定与水泥固化对Cd、Pb、Zn的处理效果、养护时间对固化体抗压强度的影响,并对飞灰的结构形貌进行了分析。结果表明,在稳定固化过程中飞灰中发生了复杂的螯合、水化反应,重金属形态由不稳定态向稳定态转变,螯合稳定对Cd的处理效果最好,水泥固化更适用于Pb、Zn。固化时间大于7 d后,飞灰中的重金属以及固化体的抗压强度已较为稳定。螯合稳定协同水泥固化的处理效果优于单一的稳定或固化方法,飞灰在固化7 d后可同时达到重金属浸出毒性和抗压强度标准,满足安全填埋要求。 相似文献
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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 总被引:24,自引:0,他引:24
Stieb DM Judek S Burnett RT 《Journal of the Air & Waste Management Association (1995)》2002,52(4):470-484
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. 相似文献
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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. 相似文献
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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. 相似文献
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David M. Stieb Stan Judek Richard T. Burnett 《Journal of the Air & Waste Management Association (1995)》2013,63(4):470-484
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. 相似文献
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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. 相似文献
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骆马湖富营养化和生态状况调查与评价 总被引:5,自引:0,他引:5
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。 相似文献
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剩余污泥浓缩脱水投药量优化和模型建立 总被引:1,自引:1,他引:0
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。 相似文献
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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. 相似文献
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N. D. Camper Kathleen Stralka H. D. Skipper 《Journal of environmental science and health. Part. B》2013,48(5):457-473
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. 相似文献