天津市文明生态村生活垃圾处理方案优选

根据天津市文明生态村生活垃圾的特点和组成成分,以垃圾的分类收集和分类处理为前提,采用费用-效益分析法和层次分析法,对填埋、堆肥和焚烧处理方案分别进行费用-效益分析和经济、技术、环境、政策综合分析。结果表明,堆肥和焚烧的费用-效益分析得分为0.96和0.786,填埋不产生效益;堆肥、焚烧和填埋的层次分析法得分为7.74、4.28和5.45,堆肥方案的得分最高,其次为填埋,天津市文明生态村生活垃圾宜采用堆肥+填埋处理方案。     

北京市生活垃圾处理的环境影响评价

目前北京市生活垃圾产生量不断增加,处理设施能力日渐不足,生活垃圾管理正面临着减量化与资源化必然趋势。在未来5～10年内,堆肥处理、焚烧处理和综合处理等方式将取代卫生填埋成为北京市垃圾处理的主要方式。本研究采用生命周期评价的方法,对北京市4处垃圾处理设施采用的不同工艺（卫生填埋、好氧堆肥、焚烧处理和综合处理）的环境影响进行比较。评价结果表明4,种处理方式中填埋、堆肥、焚烧和综合处理的环境影响负荷分别为4.82×10-2、1.10×10-21、.31×10-1和2.31×10-2,焚烧处理的总环境影响潜值最大,填埋处理次之,综合处理再次,堆肥处理最小。4种处理方式的资源耗竭系数分别为-2.39×10-51、.11×10-5、-3.45×10-4和-1.04×10-6,焚烧处理的资源耗竭系数最小。     

层次分析法在城镇污水处理厂污泥处置方案选择中的应用

首先对污泥处置技术及其投资运行成本进行简要分析;然后建立城镇污水处理厂污泥处置评估技术指标体系;最后以天津市为例,采用层次分析法计算各评估技术指标的权重,对土地利用、填埋、焚烧及建材利用4种污泥处置方案进行了综合评价。结合天津市的实际情况,土地利用为最佳处置方案。     

天氧污泥对问二氯苯的吸附性能

为了研究灭活厌氧污泥和活性厌氧污泥对问二氯苯（m-DCB）的吸附,考察了吸附平衡时间、吸附动力学、吸附等温线、吸附热力学、污泥投加量和pH对吸附m-DCB的影响。结果表明,2种污泥对m-DCB的吸附在1h内达到平衡。应用伪一级、伪二级反应动力学对实验数据进行验证,表明厌氧污泥吸附m-DCB更符合伪二级反应动力学模型。2种污泥对m-DCB的吸附都可以用Langmuir和Freundlich吸附模型拟合,但Langrnuir吸附模型的拟合结果要好于Freundlich模型,且活性厌氧污泥的吸附性能显著高于灭活厌氧污泥。从吸附热力学上看,该吸附为放热反应,低温有利于吸附反应的进行。pH值对2种污泥吸附m-DCB的影响很小。     

分类收集效益模型在农村生活垃圾处理处置中的应用

分析了农村生活垃圾处理效益的组成,据此建立了农村生活垃圾分类收集效益模型.以南通市农村为研究对象,确定了该模型中的各参数,并且利用该模型计算了方案1(回收/填埋)、方案2(回收/焚烧/填埋)和方案3(回收/焚烧/堆肥/填埋)的分类收集效益.结果表明,方案3及其分类收集方式具有良好的经济效益和环境效益.     

餐厨垃圾处置方式及其碳排放分析

在综述填埋、好氧堆肥、粉碎直排、厌氧消化产沼气及综合处置等5种餐厨垃圾处置方式原理与特点的基础上,分别罗列出各种处置方式的优缺点、应用场合以及今后仍然需要研究的方向。着眼于餐厨垃圾资源化与碳减排,厌氧消化产沼气被定位为今后餐厨垃圾处置的主要应用方向,特别是与市政污水处理剩余污泥共消化更是今后研究与应用的主流。餐厨垃圾处置全生命周期碳排放分析亦表明,厌氧消化产沼气与其他4种处置方式相比,在资源回收与碳减排方面优势明显,这就决定了厌氧消化今后在餐厨垃圾处置技术中将处于首选位置。餐厨垃圾与剩余污泥厌氧共消化产生的沼气量具有"1+12"的能量转化效果,这种方式可以使污水处理厂演变为"能源工厂"的角色,而且还能省去餐厨垃圾单独处置所需的各种设施。     

厌氧污泥对间二氯苯的吸附性能简

为了研究灭活厌氧污泥和活性厌氧污泥对间二氯苯 （m-DCB）的吸附,考察了吸附平衡时间、吸附动力学、吸附等温线、吸附热力学、污泥投加量和pH对吸附m-DCB的影响。结果表明,2种污泥对m-DCB的吸附在1 h内达到平衡。应用伪一级、伪二级反应动力学对实验数据进行验证,表明厌氧污泥吸附m-DCB更符合伪二级反应动力学模型。2种污泥对m-DCB的吸附都可以用Langmuir和Freundlich吸附模型拟合,但Langmuir吸附模型的拟合结果要好于Freundlich模型,且活性厌氧污泥的吸附性能显著高于灭活厌氧污泥。从吸附热力学上看,该吸附为放热反应,低温有利于吸附反应的进行。pH值对2种污泥吸附m-DCB的影响很小。     

基于灰色层次分析法的渗滤液浓缩液回灌填埋体评价

为科学合理地选择渗滤液浓缩液回灌的最优填埋体,采用灰色层次分析法对回灌填埋体进行了综合评价。首先构建灰色层次分析法的层次结构模型及评价指标,并根据层次分析法计算各评价指标权重,然后基于灰色关联理论建立评价指标关联系数矩阵,最后根据各评价指标权重及其关联系数矩阵建立综合评价矩阵。采用建立的综合评价方法对垃圾年份分别为1 a、5 a和15 a的回灌填埋体进行了综合评价。结果表明,垃圾年份为15 a的回灌填埋体与理想方案的关联度最大,为最优的回灌填埋体,其次为5 a、1 a。     

贝壳粉对重金属镉的吸附特征研究

研究了贝壳粉对重金属镉的吸附特征,结果表明:在镉离子质量浓度为100 mg/L时,文石型贝壳粉对镉离子的吸附能力强于方解石型贝壳粉;在文石型贝壳粉中,海虹和毛蚶的贝壳粉对镉离子的吸附性能最强。所有供试贝壳粉对镉离子的吸附过程均符合Langmuir等温吸附模型,说明该吸附过程为单分子层吸附,既存在物理吸附又存在化学吸附。贝壳粉对镉离子的动力学吸附分为快速吸附和平衡吸附两个阶段。快速吸附阶段时间较短但吸附量大,符合准一级动力学模型;而吸附全过程符合准二级动力学模型,说明贝壳粉的吸附主要在表面进行。     

北京市生活垃圾分类处理体系:Ⅰ.问题诊断

通过建立评价指标体系的方法对北京市生活垃圾分类处理体系中存在的问题进行诊断.首先,简要分析了北京市生活垃圾处理现状,在此基础上提出了北京市生活垃圾分类处理评价指标体系,进而运用层次分析法确定各评价指标的权重.并通过计算这些评价指标的权重与其未达标率之积,得出北京市垃圾分类处理体系中存在问题的严重程度排序为垃圾分类运输车配置率＞垃圾回收率＞垃圾分类收集率＞居民垃圾分类参与率＞垃圾处理设施运转率＞垃圾填埋、堆肥、焚烧所占比例＞居民垃圾分类知晓率＞垃圾分类收集容器配置率＞回收站设置的便利度＞垃圾运输能力＞垃圾无害化处理率.     

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

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.     

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.     

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.     

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。     

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。     

Experimental and statistical validation of SPME-GC-MS analysis of phenol and chlorophenols in raw and treated water

A procedure based on solid-phase microextraction (SPME) and gas chromatography coupled with mass spectrometry (GC-MS) was developed and validated in order to analyse 10 phenols in water samples. The optimised conditions were obtained using polyacrylate fibre (PA), 20ml of sample volume, 10% NaCl, pH 4.0 and direct extraction at 35 degrees C and 1000rpm, for 40min. The linear range and quantification limits for these compounds by SPME-GC-MS were defined. An evaluation of the main uncertainty sources of this method is included, which allows expanded uncertainties in the 9.4-35% range for the majority of the compounds. The main source of uncertainty is associated with matrix effects. The validated method is suitable for monitoring the production and distribution of potable water and was used, in field trials, for the analysis of samples from main intakes of water (surface or underground) and from water supply system of a large area (Lisbon and neighbour municipalities).     

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.