丹江口水库生态系统健康综合评价

2007年7月～2008年5月按季度对丹江口水库4个库区(丹江库区、汉江库区、取水口和五青入库区)的水环境和浮游生物进行了调查,采用生态系统健康指数(EHI)法和营养状态指数(TSI)法对该水库的生态系统健康状态进行定量的综合评价.结果表明:2007年7月～2008年5月,丹江口水库整体处于中营养状态,健康状态中等,健康状态总趋势是丹江库区>取水口>汉江库区>五青入库区;各库区生态系统健康状态存在季节性差异,丹江库区、取水口两库区全年为中等,汉江库区在夏季为较差,其它季节中等,五青入库区在冬季最差,其它季节较差.此外,对两种评价方法进行了比较,表明丹江口水库属于响应型生态系统,生态系统健康指数(EHI)适用于丹江口水库生态系统健康的评价.     

Arsenic in groundwaters of the Lower Mekong

Increasing incidence and awareness of arsenic in many alluvial aquifers of South-east Asia has raised concern over possible arsenic in the Lower Mekong Basin. Here, we have undertaken new research and reviewed many previous small-scale studies to provide a comprehensive overview of the status of arsenic in aquifers of Cambodia and the Cuu Long Delta of Vietnam. In general natural arsenic originates from the Upper Mekong basin, rather than from the local geology, and is widespread in soils at typical concentrations of between 8 and 16 ppm; (dry weight). Industrial and agricultural arsenic is localised and relatively unimportant compared to the natural alluvial arsenic. Aquifers most typically contain groundwaters of no more than 10 μg L⁻¹, although scattered anomalous areas of 10 to 30 μg L⁻¹ are also quite common. The most serious, but possibly ephemeral arsenic anomalies, of up to 600 μg L⁻¹, are associated with iron and organic-rich flood-plain sediments subject to very large flood-related fluctuations in water level, resulting in transient arsenopyrite dissolution under oxidizing conditions. In general, however, high-arsenic groundwaters result from the competing interaction between sorption and dissolution processes, in which arsenic is only released under reducing and slightly alkaline conditions. High arsenic groundwaters are found both in shallow water-tables, and in deeper aquifers of between 100 and 120 m depth. There is no evidence of widespread arsenicosis, but there are serious localised health-hazards, and some risk of low-level arsenic ingestion through indirect pathways, such as through contaminated rice and aquaculture. An almost ubiquitous presence of arsenic in soils, together with the likelihood of greatly increased groundwater extraction in the future, will require continuing caution in water resources development throughout the region.     

军用飞机结构类型聚类分析

选取某型飞机16个典型结构,采用温、湿度测量仪测量其局部温、湿度,测量周期为2个月,分别获得673个有效温、湿度实测数据。根据实测数据,采用模糊聚类算法对飞机结构类型进行归并分析,当模糊矩阵阈值λ=0．7时,飞机结构类型可归并为开式、半开式、封闭式3种典型结构形式。     

Nanoencapsulation of hexavalent chromium with nanoscale zero-valent iron: High resolution chemical mapping of the passivation layer

Solid phase reactions of Cr(Ⅵ) with Fe(0) were investigated with spherical-aberration-corrected scanning transmission electron microscopy(Cs-STEM) integrated with X-ray energy-dispersive spectroscopy(XEDS). Near-atomic resolution elemental mappings of Cr(Ⅵ)–Fe(0) reactions were acquired. Experimental results show that rate and extent of Cr(Ⅵ) encapsulation are strongly dependent on the initial concentration of Cr(Ⅵ) in solution. Low Cr loading in nZⅥ(1.0 wt%) promotes the electrochemical oxidation and continuous corrosion of n ZⅥ while high Cr loading(1.0 wt%) can quickly shut down the Cr uptake. With the progress of iron oxidation and dissolution, elements of Cr and O counter-diffuse into the nanoparticles and accumulate in the core region at low levels of Cr(Ⅵ)(e.g., 10 mg/L). Whereas the reacted n ZⅥ is quickly coated with a newly-formed layer of 2–4 nm in the presence of concentrated Cr(Ⅵ)(e.g., 100 mg/L). The passivation structure is stable over a wide range of pH unless pH is low enough to dissolve the passivation layer. X-ray photoelectron spectroscopy(XPS) depth profiling reconfirms that the composition of the newly-formed surface layer consists of Fe(Ⅲ)–Cr(Ⅲ)(oxy)hydroxides with Cr(Ⅵ) adsorbed on the outside surface. The insoluble and insulating Fe(Ⅲ)–Cr(Ⅲ)(oxy)hydroxide layer can completely cover the n ZⅥ surface above the critical Cr loading and shield the electron transfer. Thus, the fast passivation of nZⅥ in high Cr(Ⅵ) solution is detrimental to the performance of nZⅥ for Cr(Ⅵ) treatment and remediation.     

Measuring water resource use efficiency of the Dong Nai River Basin (Vietnam): an application of the two-stage data envelopment analysis (DEA)

Environment, Development and Sustainability - The recent growth of agriculture, industry and urban areas in Vietnam requires a large amount of water consumption as a production factor. This paper...     

能源回弹效应的研究进展及其政策涵义

“十二五”期间节能减排的目标是单位GDP能耗下降16％,为实现这一目标,政府采取了以提高能源效率为核心的节能减排政策,但是能源效率的提高可能产生潜在的“回弹效应”,即可能增加能源的使用从而使得节能减排目标难以实现.本文在文献研究的基础上,分析了回弹效应的类型和产生机理,梳理了国内外文献中关于回弹效应测度的实证结果,指出了当前实证研究中存在的主要问题,并从公共政策制定的角度设计了经济模型和其他社会科学相结合的定性比较分析研究方案,主张从经济主体行为反应、替代品价格、能源补贴以及发展新能源政策等多重视角研究回弹效应发生的内在机理,从而对能源政策产生明确的导向.最后,提出了加强能源回弹效应研究的具体政策建议.     

缺氧MBBR耦合部分厌氧氨氧化强化城市生活污水深度脱氮

缺氧MBBR是强化传统城市污水处理系统脱氮的一种方法,本研究通过向城市污水后置反硝化SBR中投加填料构建了缺氧双污泥系统,实现了城市生活污水部分厌氧氨氧化深度脱氮.在250d的运行中脱氮性能逐渐提高并实现稳定,出水总氮在5 mg·L~(-1)左右. 211～250 d的平均硝氮、氨氮和总氮去除率分别为(97. 7±2. 9)%、(93. 3±2. 9)%和(94. 3±2. 7)%.长期运行中观测到氨氮和硝氮的同步去除.针对氨氮去除途径进行分析,系统同化、硝化作用微弱.缺氧MBBR中存在厌氧氨氧化活性且对脱氮有不可忽视的作用.实时定量PCR结果进一步说明缺氧MBBR中厌氧氨氧化菌富集,特别是缺氧填料生物膜中厌氧氨氧化菌丰度由初始的4. 37×10~7copies·g~(-1)增长到了2. 28×10~(10)copies·g~(-1).本研究表明缺氧填料生物膜在厌氧氨氧化的富集强化城市污水深度脱氮中或许具有可应用的潜能.     

高校学生公寓应急疏散模拟与优化

运用应急疏散软件Pathfinder对某高校学生公寓的人员疏散进行了模拟,结果表明,休息时间段内公寓发生的突发事件更容易造成人员疏散运动时间的延长;同等条件下女生比男生所需要的人员疏散运动时间更长。通过合理规划疏散路线,对原有模型进行了优化,并使用人员疏散运动时间和单位有效疏散宽度使用率两个指标,来定量对比优化前后人员疏散的均衡度和疏散效果,给高校学生公寓的应急和安全管理工作提供参考。     

负载型Mn-Ce/TiO2催化剂的制备及其低温脱硝活性简

以成型TiO₂作为载体,通过浸渍法制备了Mn-Ce/TiO₂低温SCR催化剂,并系统研究了制备方法、煅烧条件、活性组分担载量、Mn含量等参数对催化剂催化还原NO性能的影响。结果表明,煅烧温度的升高会促使活性组分结晶度的提高,从而引起催化活性的降低,在500℃和600℃下所得Mn-Ce/TiO₂催化剂活性组分为无定型态,表现出较高的脱硝活性。活性组分担载量的增加有利于催化活性的提高。Mn含量对Mn-Ce/TiO₂催化剂的活性有较大影响,当Mn/（Mn+Ce）摩尔比为40%和85%时,催化剂活性最高。     

Esterification of sugarcane bagasse by citric acid for Pb2+ adsorption: effect of different chemical pretreatment methods

In this study, different pretreatment strategies of sugarcane bagasse prior to citric acid modification were investigated in terms of Pb²⁺ adsorption capacity. Pretreatment strategies included the use of NaOH, HCl, and C₂H₅OH in various concentrations. In order to fundamentally understand how these pretreatment methods affect the modification of sugarcane bagasse by citric acid as well as the Pb²⁺ adsorption capacity of sugarcane bagasse, three main components of sugarcane bagasse namely cellulose, hemicellulose, and lignin were isolated and esterified by citric acid under the same conditions. ATR-FTIR, XPS, SEM, and an analysis of the number of carboxylic acid groups were used to investigate the physicochemical and chemical properties of the materials. These three components were proved to participate in adsorption and induce the esterification with citric acid. Hence, pretreatment with ethanol and 0.01 M NaOH which could retain cellulose, hemicellulose, and lignin in sugarcane bagasse achieved a high Pb²⁺ adsorption capacity, i.e., 122.4 and 97 mg/g after the esterification with citric acid. In contrast, pretreatment with 0.5 M NaOH and 0.1 M HCl removed lignin and hemicellulose, leading to the lowest value of approximately 45 mg/g for citric acid esterified-pretreated sugarcane bagasse. XPS analysis and number of carboxylic group measurement confirmed the esterification between bagasse and citric acid. To understand the adsorption mechanism of adsorbent, two kinetic models including pseudo-first-order model and pseudo-second-order model were applied. The experimental data were well described by the pseudo-second-order model. The adsorption isotherm data were fitted Langmuir and Freundlich.