Chemical compositions and sources of atmospheric PM10 in heating, non-heating and sand periods at a coal-based city in northeastern China

Mass concentrations and chemical components (18 elements, 9 ions, organic carbon [OC] and elemental carbon [EC]) in atmospheric PM(10) were measured at five sites in Fushun during heating, non-heating and sand periods in 2006-2007. PM(10) mass concentrations varied from 62.0 to 226.3 μg m(-3), with 21% of the total samples' mass concentrations exceeding the Chinese national secondary standard value of 150 μg m(-3), mainly concentrated in heating and sand periods. Crustal elements, trace elements, water-soluble ions, OC and EC represented 20-47%, 2-9%, 13-34%, 15-34% and 13-25% of the particulate matter mass concentrations, respectively. OC and crustal elements exhibited the highest mass percentages, at 27-34% and 30-47% during heating and sand period. Local agricultural residuals burning may contribute to EC and ion concentrations, as shown by ion temporal variation and OC and EC correlation analysis. Heavy metals (Cr, Ni, Zn, Cu and Mn) from coal combustion and industrial processes should be paid attention to in heating and sand periods. The anion/cation ratios exhibited their highest values for the background site with the influence of stationary sources on its upper wind direction during the sand period. Secondary organic carbon were 1.6-21.7, 1.5-23.0, 0.4-17.0, 0.2-33.0 and 0.2-21.1 μg m(-3), accounting for 20-77%, 44-88%, 4-77%, 8-69% and 4-73% of OC for the five sampling sites ZQ, DZ, XH, WH and SK, respectively. From the temporal and spatial variation analysis of major species, coal combustion, agricultural residual burning and industrial emission including dust re-suspended from raw material storage piles were important sources for atmospheric PM(10) in Fushun at heating, non-heating and sand periods, respectively. It was confirmed by principal component analysis that coal combustion, vehicle emission, industrial activities, soil dust, cement and construction dust and biomass burning were the main sources for PM(10) in this coal-based city.     

改性SiO2气凝胶对废水中Fe3+的吸附性能

制备了改性SiO₂气凝胶，考察了经不同类型、不同配比的改性剂改性的SiO₂气凝胶对模拟含Fe³⁺废水的吸附处理效果。实验结果表明：改性SiO₂气凝胶的最佳制备条件为三甲基氯硅烷（TMCS）作改性剂，V（TMCS）#x02236;V（正己烷）=1#x02236;5；当改性SiO₂气凝胶加入量为75g/L、吸附时间为4h、Fe³⁺质量浓度为10mg/L时，模拟含Fe³⁺废水的Fe³⁺去除率为98.32%，剩余Fe³⁺质量浓度为0.168mg/L；采用改性SiO₂气凝胶动态吸附处理流量为420mL/h、Fe³⁺质量浓度为100mg/L的模拟含Fe³⁺废水，吸附后废水中剩余Fe³⁺质量浓度仅为0.196mg/L。     

复合沸石滤床修复北方景观水体的实验研究

以天然矿物质沸石、细砂及煤渣取代传统滤料构建复合基质生态床，表面种植景观植物，采用下向流-上向流运行方式修复北方景观水体。分别进行静态实验及不同循环速率下的动态实验，考察对水体污染物去除过程。结果表明，2种运行方式下对水体NH⁺₄-N去除率都在85%以上，其中以1 h为循环周期的运行方式去除率达97%，较静态提高12.8%；TN去除率最高为84%；TP去除不稳定，过程缓慢。煤渣层对NH⁺₄-N的去除效果差，硝化作用不彻底与反硝化作用的加强使下层出水NH⁺₄-N 、NO^-₂-N及NO^-₃-N浓度均高于上层。提高循环速率有利于对氮的去除。     

土壤中零价铁还原3-氯硝基苯的作用

利用零价铁在常温常压下对土壤中的3-氯硝基苯的还原，对反应物和产物随时间的变化及反应的各个影响因素进行了研究。实验结果表明，零价铁能够有效地将3-氯硝基苯还原为3-氯苯胺，反应过程中没有检测到脱氯产物。其反应速率随铁粉用量、反应体系含水量的增加以及反应温度的升高而升高，随土壤初始pH值的升高而降低。在土壤中3-氯硝基苯含量约为2.5×10^-6 mol/g，铁粉使用量为25 mg/g，反应体系中含水量为0.75 mL/g，pH值为6.8时，在恒温生化培养箱(25±1)℃反应5 h后，3-氯硝基苯的还原率达到92.75％。     

Insight into metal binding properties of biochar-derived DOM using EEM-PARAFAC and differential absorption spectra combined with two-dimensional correlation spectroscopy

Environmental Science and Pollution Research - A large amount of biochar-derived dissolved organic matter (BDOM) will be released into the environment with biochars application into repairing...     

Polycyclic aromatic hydrocarbon and n-alkane pollution characteristics and structural and functional perturbations to the microbial community: a case-study of historically petroleum-contaminated soil

Characterization of the typical petroleum pollutants, polycyclic aromatic hydrocarbons (PAHs) and n-alkanes, and indigenous microbial community structure and function in historically contaminated soil at petrol stations is critical. Five soil samples were collected from a petrol station in Beijing, China. The concentrations of 16 PAHs and 31 n-alkanes were measured by gas chromatography-mass spectrometry. The total concentrations of PAHs and n-alkanes ranged from 973 ± 55 to 2667 ± 183 μg/kg and 6.40 ± 0.38 to 8.65 ± 0.59 mg/kg (dry weight), respectively, which increased with depth. According to the observed molecular indices, PAHs and n-alkanes originated mostly from petroleum-related sources. The levels of ΣPAHs and the total toxic benzo[a]pyrene equivalent (ranging from 6.41 to 72.54 μg/kg) might exert adverse biological effects. Shotgun metagenomic sequencing was employed to investigate the indigenous microbial community structure and function. The results revealed that Proteobacteria and Actinobacteria were the most abundant phyla, and Nocardioides and Microbacterium were the important genera. Based on COG and KEGG annotations, the highly abundant functional classes were identified, and these functions were involved in allowing microorganisms to adapt to the pressure from contaminants. Five petroleum hydrocarbon degradation-related genes were annotated, revealing the distribution of degrading microorganisms. This work facilitates the understanding of the composition, source, and potential ecological impacts of residual PAHs and n-alkanes in historically contaminated soil.

     

AOX contamination status and genotoxicity of AOX-bearing pharmaceutical wastewater

Adsorbable organic halogens(AOX) are a general indicator for the total amount of compounds containing organically bonded halogens. AOX concentrations and components were investigated along the wastewater treatment process in four large-scale pharmaceutical factories of China, and genotoxicity based on the SOS/umu test was also evaluated. The results showed that AOX concentrations in wastewater of four factories ranged from 4.6 to 619.4 mg/L, which were high but greatly different owing to differences in the raw materials and products. The wastewater treatment process removed 50.0%–89.9% of AOX, leaving 1.3–302.5 mg/L AOX in the effluents. Genotoxicity levels ranged between 2.1 and 68.0 μg 4-NQO/L in the raw wastewater and decreased to 1.2–41.2 μg 4-NQO/L in the effluents of the wastewater treatment plants(WWTPs). One of the main products of factory I, ciprofloxacin, was identified as the predominant contributor to its genotoxicity. However, for the other three factories, no significant relationship was observed between genotoxicity and detected AOX compounds.     

闲置厌氧氨氧化微生物的启动及微生物分析

文章以闲置12个月的厌氧氨氧化生物膜填料重新启动厌氧氨氧化反应器,并对反应器的活性恢复情况、脱氮效果和微生物菌群结构开展研究。实验结果表明:在启动的200 d逐渐将进水氨氮、亚硝态氮浓度从50 mg/L提高到70 mg/L,水力停留时间从12 h缩短到4 h,后期氨氮去除率达80%以上,亚硝酸盐去除率达95%。170~200 d的稳定期中,平均去除负荷0.71±0.15 kg/(m~3·d)。另外,通过高通量测序技术对反应器中微生物群落变化情况进行了系统分析。启动过程中填料中污泥微生物浮霉菌门Planctomyctes的相对丰度从13.7%增长到了36.0%,成为优势菌群。     

基于WebGIS的水环境模拟关键技术研究

近年来随着水环境模拟领域的发展出现了较多水环境数学模型,目前日益成熟的WebGIS技术是使模型使用变得简单化和直观化的一大途径.是在通过Flex和ArcGIS Server搭建WebGIS系统平台的基础上,利用PHP进行WebGIS和水环境模拟模型的数据交互,实现系统平台和数值模型的松散耦合.用户在浏览器端进行模型输入条件的设置,模型在远程服务器端进行运行计算,反馈的模拟结果通过RIA在WebGIS中进行多元化动态展示.该方法对一般模型具有适用性,可降低模型使用门槛,提高模拟结果展示和分析能力.     

生态敏感性评价在生态文明建设中的运用研究——以四川省蓬安县为例

以四川省蓬安县为例,基于GIS空间分析技术,结合蓬安当地实际,选取水源涵养、土壤保持能力和生物多样性进行生态敏感性评价,获得蓬安县区域敏感性现状图,并以此为基础构建生态安全格局,该格局注重区域的内在机理与周围的相对联系,保证各生态环境功能区成为具有各自特点、功能和生命活力而又彼此联系的有机体,为其生态文明建设过程中重点领域和重点工程设计规划提供基础支撑,阐明了生态敏感性评价在生态文明建设中的运用,为县级生态文明建设规划做出了贡献.