2017年厦门金砖会晤期间PM2.5的化学特征及来源

为了探讨厦门金砖会晤期间的排放控制措施以及天气形势对大气颗粒物污染特征的影响,于2017年8月10日至9月10日对厦门气态污染物、细颗粒物(PM2.5)中的水溶性离子以及有机碳(OC)、元素碳(EC)等主要化学成分开展了高时间分辨率的在线监测。根据空气质量管控措施和天气形势将研究期分为6个阶段。管控前、管控期Ⅰ(非台风)和管控期Ⅱ(非台风) PM2.5质量浓度分别为(33. 12±9. 48)、(30. 30±17. 00)、(16. 01±4. 71)μg/m^3。管控期Ⅰ(台风)和管控期Ⅱ(台风) PM2.5质量浓度分别为(12. 40±3. 73)、(12. 45±3. 28)μg/m^3。结果表明:管控期Ⅰ(非台风)阶段受静稳天气的影响,管控效果削弱,PM2.5质量浓度下降幅度小;台风对颗粒物质量浓度下降的影响比管控更显著。管控初期,PM2.5中二次无机离子的质量浓度下降明显;台风对碳质组分质量浓度的影响不如无机组分显著。PMF源解析结果表明,二次无机源是PM2.5主要来源,随着管控措施的实行,扬尘源的贡献从21%降低到6%,而机动车源的贡献降幅不明显。台风期间SO4^2-、NO3^-、SO2、NO2以及硫酸盐氧化比值(SOR)均明显低于非台风期间,氮氧化比值(NOR)反而升高。台风和非台风期间NOR的日变化特征一致,NOR与阳离子的相关性分析结果表明,台风或高风速海风期间NOR与Na^+呈现很强的正相关性,说明海盐粒子可促进NO2非均相反应生成NO3-。     

外来生物入侵关键点控制管理体系——基于风险管理的研究

将风险管理理论与外来生物入侵风险分析相结合，借鉴食品质量控制中的关键点控制原理，提出了防止外来生物入侵风险的关键点控制方法。针对人类有意引种、随人类活动无意引入以及自然传入3类外来生物入侵的传入途径，在入侵途径上确定若干个风险控制关键点，有针对性地提出了相应的控制措施，以减小外来生物的入侵风险，提高我国在防止外来生物入侵方面的管理与控制效率。     

含钒石煤烧渣的稳定化试验研究

研究了含钒石煤烧渣稳定化处理的一种有效方法。利用石灰为稳定剂与烧渣相混合进行稳定化处理,渣中的水溶态钒转化为钒酸钙沉淀而降低毒性。浸出试验表明,水中钒浓度〈5mg／h,并且具有长期的稳定性,无二次污染。     

反应堆控制棒驱动机构电机温升试验研究

目的 研究电机在不同工况下的温升情况,完成电机散热能力评估,为电机散热优化和工程通风设计提供参考.方法 模拟驱动机构实际运行环境,在断风条件下进行自然散热温升试验,获取电机温升最大工作模式,并在该模式下进行2种风速条件下的通风试验,获取定子绕组的平衡温度.当定子绕组达到热平衡后,切断通风,进行断风试验,获取最大断风时间...     

基于视频识别的直接作业环节安全管控

概述了石化行业现场直接作业环节的安全管控现状,分析了现场管控过程中存在的问题。考虑现场安全管理和监督监控的实际需要,设计了石化行业直接作业现场智能化管控系统,并深入研究作业现场违章行为图像识别的关键技术。现场应用表明,系统充分体现了日常管理、实时监控、智能报警、统计分析等方面的便利性和有效性,各类违章行为图像识别准确率达到80%以上,具有一定的推广价值。     

基于风险梯度的化工企业事故风险定量评估

为了定量分析区域内重大危险源所构成的风险,为事故风险防控提供科学依据,基于风险场理论对某区域内2家化工企业进行风险分析,得出2家企业所对应的风险值计算公式,并生成2家企业所对应的风险等值面和风险等值线;引入最速下降法,利用负梯度搜寻风险的最快下降方向,得出事故的最优风险降低路径。研究结果表明:甲企业中接近1/2的区域为Ⅲ级风险区域,其余区域为Ⅱ级风险区域,乙企业中大部分区域为Ⅱ级风险区域,仅少部分区域属于Ⅲ级风险区域。相较而言,乙企业中5条最优风险降低路径里程更短,人员分配情况更为合理,更具安全优势;甲企业事故风险更大,更需要完善相关安全措施以免发生事故。     

土著致病菌及其胞外物在生物防治斑马贝中的作用

无脊椎动物斑马贝(Dreissena polymorpha) 的生物污损造成了巨大的经济损失,而应用从斑马贝体内分离出的土著菌株及其体外代谢产物对它进行生物防治是一种经济效益显著且对环境友好的方法.本文主要报导从斑马贝体内分离的土著菌株中筛选出致病菌并研究该细菌及其代谢产物对它的控制作用.在三十多种土著菌株中,中间气单胞菌( Aeromonas media),维罗纳气单胞菌(A. veronii),杀鲑气单胞菌杀鲑亚种(A. salmonicida subsp. salmonicida)和腐败希瓦氏菌(Shewanella putrefaciens)是幼体斑马贝的致命致病菌.当接种量为每只斑马贝107 个细菌时,接种中间气单胞菌、杀鲑气单胞菌杀鲑亚种和腐败希瓦氏菌的5 d 死亡率为100%,而维罗纳气单胞菌为65%.通过扫描电镜(SEM)发现,垂死的斑马贝肌肉组织被破坏并含有大量的细菌.4种细菌代谢产物的不同组分表现出对斑马贝不同的致死效果,在所研究的3种不同Mr组分中(Mr<5×103,5×103～10×103及>10×103),>10 ×103组分具有最高致死率.这些结果为控制贝类无脊椎动物的生物污损提供了新方法. 图4 参24     

A review of atmospheric mercury emissions,pollution and control in China

Mercury, as a global pollutant, has significant impacts on the environment and human health. The current state of atmospheric mercury emissions, pollution and control in China is comprehensively reviewed in this paper. With about 500-800 t of anthropogenic mercury emissions, China contributes 25%-40% to the global mercury emissions. The dominant mercury emission sources in China are coal combustion, non-ferrous metal smelting, cement production and iron and steel production. The mercury emissions from natural sources in China are equivalent to the anthropogenic mercury emissions. The atmospheric mercury concentration in China is about 2-10 times the background level of North Hemisphere. The mercury deposition fluxes in remote areas in China are usually in the range of 10-50μg·m^-2·yr^-1. To reduce mercury emissions, legislations have been enacted for power plants, non-ferrous metal smelters and waste incinerators. Currently mercury contented in the flue gas is mainly removed through existing air pollution control devices for sulfur dioxide, nitrogen oxides, and particles. Dedicated mercury control technologies are required in the future to further mitigate the mercury emissions in China.     

A red water occurrence in drinking water distribution systems caused by changes in water source in Beijing,China: mechanism analysis and control measures

A red water phenomenon occurred in several communities few days after the change of water source in Beijing, China in 2008. In this study, the origin of this problem, the mechanism of iron release and various control measures were investigated. The results indicated that a significant increase in sulphate concentration as a result of the new water source was the cause of the red water phenomenon. The mechanism of iron release was found that the high-concentration sulphate in the new water source disrupted the stable shell of scale on the inner pipe and led to the release of iron compounds. Experiments showed that the iron release rate in the new source water within pipe section was over 11-fold higher than that occurring within the local source water. The recovery of tap water quality lasted several months despite ameliora- tive measures being implemented, including adding phosphate, reducing the overall proportion of the new water source, elevating the pH and alkalinity, and utilizing free chlorine as a disinfectant instead of chloramine. Adding phosphate was more effective and more practical than the other measures. The iron release rate was decreased after the addition of 1.5 mg. L-1 orthophosphate- P, tripolyphosphate-P and hexametaphosphate-P by 68%, 83% and 87%, respectively. Elevating the pH and alkalinity also reduced the iron release rate by 50%. However, the iron release rate did not decreased after replacing chloramine by 0.5-0.8 mg. L-1 of free chlorine as disinfectant.     

Monitoring of environmental exposure to polycyclic aromatic hydrocarbons: a review

Polycyclic aromatic hydrocarbons (PAHs) are a large group of organic compounds with two or more fused aromatic rings. They have a relatively low solubility in water, but are highly lipophilic. Most of the PAHs with low vapour pressure in the air are adsorbed on particles. When dissolved in water or adsorbed on particulate matter, PAHs can undergo photodecomposition when exposed to ultraviolet light from solar radiation. In the atmosphere, PAHs can react with pollutants such as ozone, nitrogen oxides and sulfur dioxide, yielding diones, nitro- and dinitro-PAHs, and sulfonic acids, respectively. PAHs may also be degraded by some microorganisms in the soil. PAHs are widespread environmental contaminants resulting from incomplete combustion of organic materials. The occurrence is largely a result of anthropogenic emissions such as fossil fuel-burning, motor vehicle, waste incinerator, oil refining, coke and asphalt production, and aluminum production, etc. PAHs have received increased attention in recent years in air pollution studies because some of these compounds are highly carcinogenic or mutagenic. Eight PAHs (Car-PAHs) typically considered as possible carcinogens are: benzo(a)anthracene, chrysene, benzo(b)fluoranthene, benzo(k)fluoranthene, benzo(a)pyrene (B(a)P), dibenzo(a,h)anthracene, indeno(1,2,3-cd)pyrene and benzo(g,h,i)perylene. In particular, benzo(a)pyrene has been identified as being highly carcinogenic. The US Environmental Protection Agency (EPA) has promulgated 16 unsubstituted PAHs (EPA-PAH) as priority pollutants. Thus, exposure assessments of PAHs in the developing world are important. The scope of this review will be to give an overview of PAH concentrations in various environmental samples and to discuss the advantages and limitations of applying these parameters in the assessment of environmental risks in ecosystems and human health. As it well known, there is an increasing trend to use the behavior of pollutants (i.e. bioaccumulation) as well as pollution-induced biological and biochemical effects on human organisms to evaluate or predict the impact of chemicals on ecosystems. Emphasis in this review will, therefore, be placed on the use of bioaccumulation and biomarker responses in air, soil, water and food, as monitoring tools for the assessment of the risks and hazards of PAH concentrations for the ecosystem, as well as on its limitations.