低温等离子体协同催化降解废气污染物的研究进展

阐述了低温等离子体协同催化工艺流程与反应机理,探讨了反应温度、废气进口组分、废气中水蒸气含量、气体流速、气溶胶等因素对降解效果的影响。分析认为:一段式低温等离子体协同催化可改变低温等离子体特征及催化剂催化特性,但尚未解决尾气臭氧逃逸、副产物产生及放电稳定性等问题;两段式低温等离子体协同催化可提高污染物分子降解效率并减少尾气臭氧逃逸,但未能有效利用等离子体的能量,气体中的水蒸气、粉尘及反应过程中产生的气溶胶均能影响后置催化剂的催化性能;两段式低温等离子体协同催化已具备工程应用条件,还需配套高效预处理单元以降低废气中水蒸气、粉尘等对催化剂的影响。     

长江水体营养盐输入及对长江口海域营养盐浓度和结构的影响

根据2011—2014年共12次长江大通站的调查数据,分析了长江水体中溶解无机氮（DIN）、活性磷酸盐（PO₄-P）和活性硅酸盐（SiO₃-Si）浓度的季节变化规律并估算了各项营养盐入海通量,比较分析了自1960s以来通过长江输入的各项营养盐通量变化及对长江口海域营养盐浓度和结构的影响。结果表明,长江水体中DIN浓度夏秋高、冬春低,而PO₄-P浓度则呈现秋冬高、春夏低的变化特点,SiO₃-Si浓度与总悬浮颗粒物浓度显著相关,但无明显季节变化。DIN、SiO₃-Si通量与长江径流变化一致,呈现夏季高、冬季低的变化特征;PO₄-P通量则呈现秋季高、冬季低的变化特征。自1960s以来,DIN和PO₄-P通量均呈上升趋势,2010s较1960s分别增加9.5倍和3.6倍,而SiO₃-Si通量呈下降趋势,2010s较1960s减少0.6倍;导致长江口海域DIN和PO₄-P年均浓度分别升高4.5和0.8倍,SiO₃-Si年均浓度则下降0.6倍,氮磷比升高两倍,硅氮比和硅磷比分别降低0.9和0.8倍,这可能是导致近60 a来长江口海域赤潮发生面积增加和硅藻比例减少的原因之一。     

大连市居民头发典型重金属富集特征研究

测定了大连市居民102份头发样品中Pb、Cd、Hg、As等重金属含量,评估了其暴露风险,并对头发中重金属的含量与年龄、性别的关系进行了分析.结果表明,大连市居民头发中Pb、Cd、Hg、As含量均低于中国居民头发中重金属的建议正常值上限,4种重金属暴露风险较低.男性头发中Cd、Pb和As的平均含量明显高于女性(p0.05),其中As平均含量差异达到极显著水平(p0.01).PCA分析显示样本分布集中在第一排序轴和第二排序轴中间,表明性别并不是影响头发中重金属含量的主要因素.19～35岁年龄组居民头发中Cd和Pb含量最高,且均与56～75岁年龄组呈现显著差异(p0.05);As和Hg在56～75岁年龄组居民头发中含量最高,与其它组比较均达到了显著水平(p0.05).PCA和Pearson分析表明4种重金属间相关性较好,大连市居民对4种重金属暴露途径基本相同.     

Potential of secondary aerosol formation from Chinese gasoline engine exhaust

Light-duty gasoline vehicles have drawn public attention in China due to their significant primary emissions of particulate matter and volatile organic compounds(VOCs). However,little information on secondary aerosol formation from exhaust for Chinese vehicles and fuel conditions is available. In this study, chamber experiments were conducted to quantify the potential of secondary aerosol formation from the exhaust of a port fuel injection gasoline engine. The engine and fuel used are common in the Chinese market, and the fuel satisfies the China V gasoline fuel standard. Substantial secondary aerosol formation was observed during a 4–5 hr simulation, which was estimated to represent more than 10 days of equivalent atmospheric photo-oxidation in Beijing. As a consequence, the extreme case secondary organic aerosol(SOA) production was 426 ± 85 mg/kg-fuel, with high levels of precursors and OH exposure. The low hygroscopicity of the aerosols formed inside the chamber suggests that SOA was the dominant chemical composition. Fourteen percent of SOA measured in the chamber experiments could be explained through the oxidation of speciated single-ring aromatics. Unspeciated precursors, such as intermediate-volatility organic compounds and semi-volatile organic compounds, might be significant for SOA formation from gasoline VOCs. We concluded that reductions of emissions of aerosol precursor gases from vehicles are essential to mediate pollution in China.     

Regionalization based on spatial and seasonal variation in ground-level ozone concentrations across China

Owing to the vast territory of China and strong regional characteristic of ozone pollution,it's desirable for policy makers to have a targeted and prioritized regulation and ozone pollution control strategy in China based on scientific evidences. It's important to assess its current pollution status as well as spatial and temporal variation patterns across China.Recent advances of national monitoring networks provide an opportunity to insight the actions of ozone pollution. Here, we present rotated empirical orthogonal function(REOF)analysis that was used on studying the spatiotemporal characteristics of daily ozone concentrations. Based on results of REOF analysis in pollution seasons for 3 years' observations, twelve regions with clear patterns were identified in China. The patterns of temporal variation of ozone in each region were separated well and different from each other, reflecting local meteorological, photochemical or pollution features. A rising trend in annual averaged Eight-hour Average Ozone Concentrations(O_3-8 hr) from 2014 to 2016 was observed for all regions, except for the Tibetan Plateau. The mean values of annual and 90 percentile concentrations for all 338 cities were 82.6 ± 14.6 and 133.9 ± 25.8 μg/m~3,respectively, in 2015. The regionalization results of ozone were found to be influenced greatly by terrain features, indicating significant terrain and landform effects on ozone spatial correlations. Among 12 regions, North China Plain, Huanghuai Plain, Central Yangtze River Plain, Pearl River Delta and Sichuan Basin were realized as priority regions for mitigation strategies, due to their higher ozone concentrations and dense population.     

增压站低频噪声识别与控制

目的解决天然气增压站低频噪声严重的问题,识别低频噪声源,并对低频噪声加以控制。方法结合压缩机组的实际工作情况及结构,首先利用频谱及1/3倍频程分析增压站机组的振动和噪声特性,初步确定压缩站机组低频噪声与机组振动的关系,进一步利用相干函数分析法分析振动与低频噪声的相干关系,判定低频噪声并不是由振动主要引起的。结果机组的主要噪声源为冷却器和压缩缸的进排气管,低频噪声污染主要是由于机组周期性吸排气时,管道和机组壁投射出的空气动力性噪声所造成的,而机组振源的剧烈振动不是产生低频噪声污染的主要原因。进排气管可产生高达80 d B(A)的全频带噪声,其中包含声压级可高达100 dB的次声,尤其以频率11 Hz和17 Hz为主,并且传播距离远,通透力强,对人员和环境危害大。结论首先依据进排气管为主要噪声源,其次结合压缩站实际情况,从压缩器机组整体的降噪设计及厂房治理的降噪设计两部分考虑提出相应的改进措施,从而为机组的降噪提供有效的方法。     

环境升温过程对常温固化环氧树脂热力学性能的影响

目的提高常温固化环氧树脂体系的高温使用性能。方法采用常温固化剂T31、中温固化剂IPDA以及高温固化剂DDM作为混合固化剂,对E-44型和AG-80型混合环氧树脂体系进行常温固化反应,并分析环境升温过程对固化物热力学性能的影响。通过DMA分析、热变形测量、固化度测试,分别评价室温固化环氧树脂在环境升温过程前后的玻璃化转变温度、热变形量及体系内部的固化反应程度变化,并通过吸水率测试和弯曲强度测试对玻璃纤维布增强常温固化环氧树脂基复合材料的耐湿热性能以及高温条件下的力学性能进行分析。结果环氧树脂常温固化物的tg为85.21℃,经1.5℃/min的平均升温速率加热至90℃之后,该环境升温过程使固化物的固化度增大至92%以上,tg增长为132.06℃的同时热变形温度增大。其复合材料耐湿热性能提高,且100℃时弯曲强度的保持率为65%,对于加热至120℃的环境升温过程,固化物的固化度接近96%,tg增长为144.45℃的同时热变形温度进一步提高,其复合材料耐湿热性能改善程度更加明显,且130℃时弯曲强度保持率仍接近60%。结论常温、中温、高温混合固化剂的合理复配有助于环氧树脂体系在环境升温变化的诱导条件下发生梯度式固化反应,使体系内部的交联固化程度迅速升至较高水平,可以有效提高其玻璃化转变温度,显著改善常温固化环氧树脂体系在高温条件下的热力学性能。     

不同区域城市空气O3和PM2.5累积速率时序模型

利用2017—2018年全国7个区域10个典型城市环境空气O₃和PM_2.5浓度数据，统计污染物累积速率，进而采用回归方法拟合污染物浓度及其累积速率的时间序列模型，分析不同区域污染物时序变化特征差异。结果表明：不同区域O₃浓度时序曲线拟合程度总体高于PM_2.5，石家庄O₃拟合程度最高，西安PM_2.5拟合程度最高。以07：00、14：00分别作为O₃、PM_2.5模拟起点是24 h中的最优模型。不同城市夏季O₃小时浓度时序变化曲线均为单峰形态，O₃浓度及累积速率峰值出现时间可能由城市所处经度决定，太原O₃累积最快，西安O₃消解最快。各城市间冬季PM_2.5小时浓度及其累积速率时序变化曲线形态差异较大，沈阳PM_2.5累积和消解均最快。与浓度相比，城市环境空气O₃和PM_2.5累积速率与光照、扩散条件等有更好的时间相关性。     

大气环境质量模糊评价的可视化实现

以模糊聚类法为算法基础,运用计算机可视化技术,进行大气环境质量评价初步探索。计算机技术在环境评价中的应用,可以方便数据处理和资源共享。选用武汉市大气环境监测资料,应用该方法评价和分析武汉市大气环境质量,取得了令人满意的结果。