蒽醌类有机质对针铁矿异化还原解离特征影响

基于希瓦氏金属还原菌(Shewanella decolorationis S12)和针铁矿相互作用,讨论了蒽醌类有机质(AQS)对该针铁矿异化还原过程的调控机制.结果表明:AQS作为电子运移载体,使得还原解离态铁总量(Fetot)和可溶态铁含量(Fedis)均快速增加;不同含量的AQS加入前后,针铁矿还原平均速率得到显著上升,速率比在2.4~4.0之间,且该比值和AQS含量呈显著的线性关系,可决系数为0.9947.Fedis/Fetot比值随AQS含量升高而降低,当AQS含量由0.05 mmol·L-1增加至0.3 mmol·L-1时,Fedis/Fetot比值由0.935减小至0.705.Feads含量随AQS含量增加而增加,当体系中无AQS时,Feads含量维持在较低的水平(0.05 mmol·L-1).AQS参与下的铁异化还原过程实际上是由两个独立的子过程组成,即微生物呼吸作用驱动了AQS和还原态蒽二酚(AH2QS)的循环转变过程以及AH2QS进一步还原解离针铁矿的非生物过程.     

渭河陕西段潜流带沉积物重金属变化初步分析

为厘清潜流带沉积物重金属时空变化及与水量交换、沉积物颗粒结构间的关系,于2013年春夏两季对渭河陕西段5个研究断面66个测试点位沉积物的野外原位渗透系数、颗粒粒径、重金属含量进行分析.结果表明:影响渭河沉积物渗透系数的主要因素是沉积物粒径,同时沉积物垂向分层、排列组合也影响其渗透性能;沉积物重金属Cu、Zn、Pb、Cd质量分数在垂向上不同深度其含量大小不同,在时间上总体呈现春季夏季,富集系数(EF指数)分析结果显示春季Cu、Zn(除华县)、Pb(除眉县)、Cd富集严重且主要受人为输入源影响,夏季除Cd元素外,Cu、Zn、Pb的EF值均1.5,说明其含量主要来源于地壳和岩石圈的自然风化过程;Pearson相关分析发现粘土与粉砂(粒径0.075 mm)百分比与沉积物重金属质量分数呈弱相关,重金属粒径效应不显著,粒径不是控制重金属含量的主要环境影子;对单一重金属垂向不同深度含量进行相关性研究发现除Cd外,其余3种重金属在垂向上的相关系数均0.5(p0.01),说明单一重金属在垂向上具有同源性且存在相互迁移与转化.     

甲醇柴油双燃料燃烧结合DOC/POC耦合大幅度减少发动机微粒排放的研究

对一台四缸增压中冷柴油机采用甲醇柴油双燃料模式,研究了甲醇替代率和柴油机氧化催化转化器耦合微粒催化转化器(DOC+POC)后处理装置对该发动机烟度和微粒数量、质量浓度的粒径分布特性的影响.试验结果表明,随甲醇替代率的增加,发动机烟度和微粒数浓度、质量浓度均有不同程度的降低,核态微粒浓度显著降低,聚集态微粒浓度基本保持不变.相比于DOC+POC对纯柴油发动机排气烟度25%左右的净化效率,在甲醇柴油双燃料模式下DOC+POC对排气烟度的平均净化效率在60%以上,最大达到96%,显示了该后处理技术在甲醇柴油双燃料模式下清洁排放的良好应用前景.     

Characteristics of secondary inorganic aerosol and sulfate species in size-fractionated aerosol particles in Shanghai

Sulfate, nitrate and ammonium(SNA) are the dominant species in secondary inorganic aerosol, and are considered an important factor in regional haze formation. Size-fractionated aerosol particles for a whole year were collected to study the size distribution of SNA as well as their chemical species in Shanghai. SNA mainly accumulated in fine particles and the highest average ratio of SNA to particulate matter(PM) was observed to be 47% in the fine size fraction(0.49–0.95 μm). Higher sulfur oxidation ratio and nitrogen oxidation ratio values were observed in PM of fine size less than 0.95 μm. Ion balance calculations indicated that more secondary sulfate and nitrate would be generated in PM of fine size(0.49–0.95 μm). Sulfur K-edge X-ray absorption near-edge structure(XANES) spectra of typical samples were analyzed. Results revealed that sulfur mainly existed as sulfate with a proportion(atomic basis) more than 73% in all size of PM and even higher at 90% in fine particles. Sulfate mainly existed as(NH4)2SO4 and gypsum in PM of Shanghai. Compared to non-haze days, a dramatic increase of(NH4)2SO4 content was found in fine particles on haze days only, which suggested the promoting impact of(NH4)2SO4 on haze formation. According to the result of air mass backward trajectory analysis, more(NH4)2SO4 would be generated during the periods of air mass stagnation. Based on XANES, analysis of sulfate species in size-fractionated aerosol particles can be an effective way to evaluate the impact of sulfate aerosols on regional haze formation.     

Fenton氧化深度处理石化废水厂二级出水研究

采用连续流Fenton氧化对石化废水处理厂二级出水进行了处理试验,研究了药剂投量对COD及磷处理效果的影响,同时对处理过程中有机物的变化特性进行了分析.结果表明,原水COD平均为64.8 mg·L-1,PO3-4-P平均为0.79 mg·L-1,当H2O2(30%)投加量为0.4 m L·L-1,Fe SO4·7H2O的投加量为0.8 g·L-1,PAM投加量为0.9 mg·L-1,停留时间为30 min时,COD的平均去除率为24.3%,出水COD低于50 mg·L-1,PO3-4-P平均去除率为95.5%,原水中相对分子质量小于1×103的有机物占80.4%,Fenton氧化处理后该部分比例增加至95.6%.三维荧光分析结果表明,Fenton氧化对水中蛋白类、酚类去除效果显著.GC-MS结果表明,石化二级出水中检出主要有机物约117种,氧化后检出27种,含不饱和键类有机物去除明显.Fenton氧化可用于石化二级出水的深度处理.     

隧道工人的PM10职业暴露特征调查分析及其健康风险评价

针对隧道工人职业健康风险缺乏定量评价方法的现状,借鉴公共环境健康领域暴露评价模型对隧道施工PM10职业暴露的健康风险进行定量评价.设计职业暴露问卷对湖北麻竹高速公路某标段施工中的250名隧道工人进行了调查,并对现场PM10浓度水平进行了监测.结果表明,隧道工人的PM10暴露浓度水平相当高,开挖工、爆破工、支护工、出渣工、二衬工的PM10暴露浓度分别为限值的83倍、18倍、8倍、9倍和9倍;5个工种比较,二衬工日均暴露时间最长,达11.48 h·d-1,能量代谢率最高,达1 067.43 k J·(m2·h)-1,呼吸速率的计算结果显示除二衬工属于重度活动以外,其他4个工种均为中度活动;评价结果显示5个工种均存在健康风险,其中,PM10暴露浓度高是开挖工和爆破工危险系数高的主要原因,而二衬工危险系数高的原因则在于高劳动强度所致的较高的呼吸速率以及较高的日均暴露时间.降低隧道工人PM10健康风险可行的途径是通过配备合适劳动作业的呼吸防护用品从而降低PM10暴露浓度,另外可通过制定相应的职业规范设置合理的劳动年限从而减少持续暴露时间.     

结合激光雷达分析2014年春季南京地区一次大气污染过程

利用环境监测数据、气象数据以及数值模拟结果,结合激光雷达数据反演的气溶胶消光系数,分析了2014年5月26日至6月1日南京地区一次典型的大气污染过程.本次污染过程受到外源性沙尘和烟尘输入以及本地污染排放叠加影响.气象因素对污染物的生消起到了重要作用,低压、逆温等因素阻碍污染物扩散,最终强降雨的出现使本次污染过程终结.整个污染过程中大气边界层高度偏低且变化不大,大气形势稳定,污染物扩散困难.激光雷达可以有效探测气溶胶的垂直分层结构,能直观准确地反映出污染物的分布聚集情况以及时空变化,对大气污染监测具有重要意义.     

Investigation of trace element atmospheric pollution by nuclear analytical techniques at a global scale: harmonized approaches supported by the IAEA

In the framework of the IAEA programmes, Member States involved in air pollution studies using nuclear analytical techniques have harmonized their methodologies. Participants characterising chemical composition of size fractionated airborne particulate matter based their methodology on a common type of air sampler, centralised data collection and evaluation, and the same kind of data processing. Institutions involved in biomonitoring air pollution identified appropriate organisms to be applied at a regional scale, and harmonized procedures for sample preparation and analysis, as well as data processing and presentation. Both metrology approaches have been validated and disseminated in many Member States.     

从分子质量的变化分析有机物对GAC吸附内分泌干扰物(BPA)的影响

从分子质量分布的角度研究了水中有机物对颗粒活性炭(GAC)吸附双酚A(BPA)容量及吸附速率的影响.结果表明,相对于以去离子水为本底的BPA溶液来说,GAC吸附以滤后水、臭氧后出水和原水为本底的BPA溶液的Langmuir模型的最大吸附容量q_m值分别下降了29.95%、43.56%和44.44%,而其拟二级动力学模型的k₂值分别下降了43.05%、49.75%和56.38%.相对分子质量3 000以上,尤其是10 000以上的有机物堵塞GAC的二级微孔;3 000以下,尤其是1 000以下的有机物与BPA分子之间存在直接的竞争吸附,是导致GAC对BPA的吸附容量以及吸附速率下降的主要原因.     

Sorption of organic pollutants by marine sediments: implication for the role of particulate organic matter

The objective of this study was to quantify sorption properties for kerogen/black carbon (BC)-bearing sediments. Single-solute sorption isotherms were measured for five pristine marine sediments using phenanthrene, naphthalene, 1,3,5-trichlorobenzene, and 1,4-dichlorobenzene as the sorbates. The results showed that the sorption isotherms were nonlinear and that the organic carbon normalized single point K_OC values were comparable to those reported in the literature for the purified keorgen and BC, but are much higher than the data reported for HA and kerogen/BC-containing terrestrial soils and sediments. It is likely that koergen and BC associated with these pristine marine sediments may not be encapsulated with humic acids or Fe and Mn oxides and hydroxides as often do in terrestrial soils and sediments. As a result, they may be fully accessible to sorbing molecules, exhibiting higher sorption capacities. The study suggests that competition from background HOCs and reduced accessibility when kerogen and BC are associated with terrestrial sediments may dramatically increase variability of sorption reactivities of geosorbents. Such variability may lead to large uncertainties in the prediction of sorption from the contents of kerogen and/or BC along with TOC.