青藏高原背景站大气VOCs浓度变化特征及来源分析

采用大气预浓缩与气象色谱/质谱联用法,对2013-09-13到2013-10-14期间在国家大气背景站青海门源站所采集的大气样品进行分析.结果显示,本次研究共检测出38种挥发性有机物(VOCs),其中烷烃16种,烯烃11种,芳香烃9种,卤代烃2种.从组成成分来看,烷烃所占比例最大,达58.6%,烯烃和芳香烃分别占29%和10.5%,卤代烃所占比例最小,仅为1.7%.观测期间大多数VOCs物种呈现白天浓度低、夜晚浓度高的变化趋势,具有明显的高原站点特性,但异戊烷、异戊二烯、甲苯则呈现相反趋势.采用臭氧生成潜势(OFP)对VOCs各组分活性进行分析,各类VOCs中烯烃对OFP贡献最大.利用主成分分析VOCs物种,提取出4个因子,分别归类于燃烧源、天然气和液化石油气的泄露、工业源、生物源.结合HYSPLIT 4.0后向轨迹模型,进一步确定气团的来源与运输途径,发现来自南向的污染源贡献是门源地区VOCs物种浓度增加的主要原因.     

Removal of 2-ClBP from soil–water system using activated carbon supported nanoscale zerovalent iron

We explored the feasibility and removal mechanism of removing 2-chlorobiphenyl(2-Cl BP)from soil–water system using granular activated carbon(GAC) impregnated with nanoscale zerovalent iron(reactive activated carbon or RAC).The RAC samples were successfully synthesized by the liquid precipitation method.The mesoporous GAC based RAC with low iron content(1.32%) exhibited higher 2-Cl BP removal efficiency(54.6%) in the water phase.The result of Langmuir–Hinshelwood kinetic model implied that the different molecular structures between 2-Cl BP and trichloroethylene(TCE) resulted in more difference in dechlorination reaction rates on RAC than adsorption capacities.Compared to removing2-Cl BP in the water phase,RAC removed the 2-Cl BP more slowly in the soil phase due to the significant external mass transfer resistance.However,in the soil phase,a better removal capacity of RAC was observed than its base GAC because the chemical dechlorination played a more important role in total removal process for 2-Cl BP.This important result verified the effectiveness of RAC for removing 2-Cl BP in the soil phase.Although reducing the total RAC removal rate of 2-Cl BP,soil organic matter(SOM),especially the soft carbon,also served as an electron transfer medium to promote the dechlorination of 2-Cl BP in the long term.     

Synthesis and kinetics investigation of meso-microporous Cu-SAPO-34 catalysts for the selective catalytic reduction of NO with ammonia

A series of meso-microporous Cu-SAPO-34 catalysts were successfully synthesized by a one-pot hydrothermal crystallization method, and these catalysts exhibited excellent NH_3-SCR performance at low temperature. Their structure and physic chemical properties were characterized by means of X-ray diffraction patterns(XRD), Scanning electron microscopy(SEM), Transmission electron microscopy(TEM), N_2 sorption-desorption, nuclear magnetic resonance(NMR), Inductively Coupled Plasma-Atomic Emission spectrometer(ICP-AES), X-ray absorption spectroscopy(XPS),Temperature-programmed desorption of ammonia(NH_3-TPD), Ultraviolet visible diffuse reflectance spectroscopy(UV-Vis DRS) and Temperature programmed reduction(TPR).The analysis results indicate that the high activities of Cu-SAPO-34 catalysts could be attributed to the enhancement of redox property, the formation of mesopores and the more acid sites. Furthermore, the kinetic results verify that the formation of mesopores remarkably reduces diffusion resistance and then improves the accessibility of reactants to catalytically active sites. The 1.0-Cu-SAPO-34 catalyst exhibited the high NO conversion( 90%) among the wide activity temperature window in the range of 150–425℃.     

重金属对秀丽隐杆线虫繁殖的影响

为了探究重金属单独及联合暴露对秀丽隐杆线虫(Caenorhabditis elegans)繁殖的影响及其作用机制,采用96孔板液相暴露试验,以环境相关浓度(0.1~50.0 μg/L)的Cd、Hg、Pb暴露同步化处理秀丽隐杆线虫,24 h后统计其怀卵数及阴门畸形率,以及连续记录72 h内子一代秀丽隐杆线虫的个体数,最后利用2×2析因设计方差分析阐明重金属的两两联合作用模式. 结果表明:与对照组相比,Cd、Hg、Pb单独及联合暴露对秀丽隐杆线虫的繁殖具有显著抑制作用,ρ(Cd)为50.0 μg/L、ρ(Hg)为10.0 μg/L、ρ(Pb)为50.0 μg/L暴露组秀丽隐杆线虫子一代数量分别降低了43.5%、33.8%、51.0%;Cd-Hg暴露组〔当ρ(Cd)、ρ(Hg)分别为50.0、10.0 μg/L时〕、Hg-Pb暴露组〔当ρ(Hg)、ρ(Pb)分别为10.0、50.0 μg/L时〕、Cd-Pb暴露组〔当ρ(Cd)、ρ(Pb)分别为50.0、50.0 μg/L时〕秀丽隐杆线虫子一代个体数分别降低了44.7%、61.0%、53.3%. 进一步研究发现,Cd、Hg、Pb单独及联合暴露会引起秀丽隐杆线虫子宫内受精卵数量降低以及产卵器阴门结构畸形率升高. 2×2析因设计方差分析结果发现,Cd、Hg、Pb两两联合暴露对秀丽隐杆线虫的繁殖表现为没有交互作用或者交互方式为拮抗. 研究显示,秀丽隐杆线虫子宫内怀卵数的降低是其子一代数量显著减少的主要原因,而阴门结构的损伤可能使产卵行为受损,从而进一步加剧重金属对秀丽隐杆线虫繁殖的抑制作用.      

流域水生态安全评估方法

为建立合理的流域水生态安全评估指标体系,以流域为对象,对水生态安全内涵进行了阐释,并对流域水生态安全评估指标进行了系统分析.基于“压力、状态、功能、风险”四要素,构建了“目标层-方案层-要素层-指标层”的评估体系,其中方案层包括水生态压力、水生态状况、水生态功能和水生态风险4个方面,涵盖土地利用、水资源利用、污染物排放、栖息地状态、水生态质量、水产品供给、休闲娱乐、水环境净化、重金属风险等9个评估要素18个评估指标,并详尽表述了各评估指标的内涵及其计算方法.采用综合指数法计算ESI(生态安全指数),并根据ESI得分将水生态系统的安全评级分为安全(3.5≤ESI≤4.0)、较安全(2.5≤ESI<3.5)、一般(1.5≤ESI<2.5)、不安全(0.5≤ESI<1.5)和很不安全(0≤ESI<0.5)5个级别,构建了多指标的流域水生态安全评估方法.      

飞灰添加对沥青铺路烟气PAHs释放的影响

为评估生活垃圾焚烧飞灰替代矿粉生产沥青混合料及其路面浇筑全过程中PAHs的环境风险,采用实验室模拟与实际铺筑过程相结合的方法,改变飞灰添加量(以w计,0、3%、4%和5%)和加热温度(200、165、145和80 ℃),以对PAHs的释放规律进行研究. 结果表明:在实际筑路过程中,PAHs的释放受加热温度的影响较大,ρ(∑₁₆PAHs)随加热温度的下降而降低,其中混合料制备和道路开放使用阶段的ρ(∑₁₆PAHs)分别为249.0～378.0、72.1～95.1 μg/m3;但在路面浇筑阶段ρ(∑₁₆PAHs)有增加的趋势,为254.0～571.0 μg/m3,并且在该阶段内ρ(4环PAHs)降低,低环(2～3环)和高环(5～6环)的PAHs质量浓度升高. 飞灰的添加抑制了PAHs的释放,w(∑₁₆PAHs)在10.4～12.3 μg/kg之间,毒性当量浓度(以TEQ计)在0.011 μg/kg左右. 飞灰的添加抑制了以萘为主的低环PAHs的释放,并且在3%添加量时对PAHs的抑制效果最好;在飞灰添加量为3%、4%和5%时,w(萘)分别降低了42.7%、32.2%和35.3%.      

人工湿地在天津生态城水系构建中的应用建议研究

人工湿地技术融合基质、植物、微生物及工程构造为一体,通过物理、化学、生物、生态过程的综合作用,可以对低污染水具有良好的净化效果.在总结该技术主要工程形式、应用研究进展及常见问题的基础上,结合天津生态城水环境建设现状,以景观水体水质保持为核心目标,提出了人工湿地系统多途径多层次技术的应用方案,形成以大型人工湿地工程为依托的水系构建总体工程方案,这样就可以为该技术在黑臭水体治理及海绵城市建设领域的广泛应用提供参考依据.     

How China’s current energy pricing mechanisms will impact its marginal carbon abatement costs?

Economic and social costs and benefits are critical factors affecting greenhouse gas abatement activities. Recognizing that energy prices are one of the most important factors influencing abatement costs, this study improved the basic China Energy and Environmental Policy Analysis (CEEPA) model by introducing a current energy pricing mechanism for China. The improved model was applied to generate marginal abatement cost (MAC) curves for China including the current energy pricing mechanism and to analyze MACs for the whole country and main abatement sectors in China under different energy pricing mechanisms. The results show that China MACs are sensitive to pricing mechanisms for electricity and refined oil. Ignoring the current regulation of these prices will lead to MAC underestimation, and price liberalization of these two energy sources could lead to a decrease in China MACs. Under a 50 % emission reduction target, if the electricity price regulation is ignored, the China MAC is underestimated by almost 16 %. Energy pricing reforms will lead to variations in sectoral abatement costs and overall abatement potential, and these impacts are projected to be large in the electricity sector. Under a 50 % reduction target, if the electricity price regulation is liberalized, MAC for the electricity sector nearly will decrease 50 %.     

7A52铝合金干湿交替情况下电偶腐蚀行为研究

目的研究海洋环境下7A52铝合金在干湿周浸使用过程中的电偶腐蚀现象。方法实验配制3.5%的Na Cl水溶液浸泡试样,实验周期为504 h,全浸试样作为对比试样,在实验周期内一直浸泡在Na Cl水溶液中。测试试样干湿周浸情况下7A52与5A06,38Cr Si之间的电偶电流及电偶电压,使用SEM分析腐蚀后的表面形貌。结果 7A52-5A06干湿周浸试样电偶电流变化不大,全浸试样电偶电流较初期变化较大,后期电偶电流的大小只有初期电偶电流大小的1/8左右,7A52-38Cr Si全浸试样与干湿交替情况下电偶电流基本相同。随着试验的进行,干湿交替及全浸情况下电偶电流的差异逐渐变大,电偶电流增大约为实验初期的10倍;全浸情况下试样表面腐蚀产物较致密,干湿周浸情况下腐蚀产物较为疏松。结论在3.5%的Na Cl水溶液干湿周浸情况下,7A52-5A06,7A52-38Cr Si的平均电偶腐蚀速度要大于全浸状态下的平均电偶腐蚀速度,干湿周浸情况下,7A52-5A06,7A52-38Cr Si腐蚀后试样表面形态具有较大差异,5A06在相同实验条件下的耐腐蚀性要好于7A52。     

基于数字图像相关方法的石墨高温杨氏模量测试

目的为了得到石墨在高温环境下的杨氏模量,为飞行器热防护系统和高温热结构的设计提供可靠的技术保障。方法基于数字图像相关(DIC)方法和通电电阻加热技术,建立一套测量材料在高温环境下力学性能的测试系统。利用该系统,测量高温下石墨试样的表面应变场和应力-应变曲线,计算相应温度下的杨氏模量。在1400℃实验环境下,采用基于DIC与高温引伸计的方法同时测量超高温陶瓷试件的拉伸应变数据,并进行比较验证。结果在1400℃实验环境下,采用基于DIC与高温引伸计方法测得超高温陶瓷的应变-时间曲线吻合良好,方差为1.3×10-7。1200~1900℃高温环境下,石墨的杨氏模量随温度的升高呈线性增长趋势。结论采用基于DIC方法准确有效,该方法可方便快速地实现对石墨材料在高温环境下杨氏模量的测量。另外,该方法也可应用于其他导电材料杨氏模量的测试。