Heavy metals and arsenic fixation into freshwater organic matter under Gammarus pulex L. influence

Organic sediments are a main sink for metal pollutants in aquatic systems. However, factors that make sediments a sink of metals and metalloids are still not clear. Consequently, we investigate the role of invertebrate shredders (Gammarus pulex L.) on quality of metal and arsenic fixation into organic partitions of sediment in the course of litter decay with laboratory microcosm experiments. During the decomposition of leaf litter, G. pulex significantly facilitated the development of small particles of organic matter. The capacity of metal fixation was significantly higher in smaller particles than leaf litter and litter residuals. Thus, G. pulex enhanced metal fixation into the organic partition of sediments by virtue of increasing the amount smaller particles in the aquatic system. Furthermore, invertebrates have a significant effect on formation of dissolved organic matter and remobilization of cobalt, molybdenum and cesium, but no significant effect on remobilization of all other measured elements.     

非织造布的防辐射性能对比研究

本文比较了80g／m^2复合法（SMS）非织造布经涂层与未经涂层两种试样对90Sr放射源的防护性能，结果显示经涂层非织造布的屏蔽率提高很大。分析表明，涂层剂对提高屏蔽率的作用要显著高于单纯增加厚度和克重来提高屏蔽率。     

镉在日本无刺楤木叶片的积累与对其抗氧化系统的影响

为考察镉对日本无刺楤木(Aralia elata var. inermis)生长及品质安全性的影响,采用生物盆栽法研究镉处理对不同生长期楤木叶片抗氧化系统影响及与镉含量关系。结果表明:展叶末期楤木叶片镉含量较少,镉对楤木叶片抗氧化能力有促进作用,随着处理量增加,叶片过氧化物酶(POD)活性、叶绿素含量先增大后减小,镉对过氧化氢酶(CAT)活性影响较强,可使其降至对照的30%,丙二醛(MDA)含量呈一定的先下降后上升的变化。生长中期POD活性达整个生长期最低;随着镉处理量增加,CAT活性先增强后减弱,但明显高于对照;叶绿素含量降幅各生长期最大,最低为对照69.1%;MDA含量则有显著增加。落叶初期叶片镉含量达到同处理最大;随着镉处理量的增加,POD活性持续减弱,CAT活性先增强后减弱,所受影响小于生长中期;叶绿素含量持续下降;落叶初期MDA含量在低量镉处理中降低,高量镉处理下继续升高。     

酚类内分泌干扰物的污染现状及处理研究进展

为了更好的治理水体中pEDCs的污染,针对pEDCs的代表物质双酚A和烷基酚,综述了世界范围内污染源水中pEDCs的污染现状,并介绍了吸附法、膜处理法、生物降解法、化学氧化法及高级氧化法等主要处理方法。同时,展望了今后pEDCs处理的主要研究方向及现存处理方法的应用前景。两种或两种以上方法的联用将是未来研究的一个重要方向。     

“空地一体化”环境应急监测与管理系统设计

在总结我国环境应急管理体系建设现状的基础上,提出了"空地一体化"的环境应急监测与管理体系的框架和功能设计,介绍了引入无人机监测系统对环境应急体系的功能改进。最后从无人机机载传感器、"空地一体化"数据分析处理和通讯保障3个维度对关键技术的选择问题进行了探讨,分析了其现状、技术难点与发展趋势,以期为现代化的环境应急体系建设提供有益的参考。     

中国大气挥发性有机物控制现状及对策研究

大气挥发性有机物(VOCs)不仅本身具有较强毒性,而且是影响中国区域复合大气污染的重要前体物和参与物。近年来,中国不断加大对VOCs的管控力度,从制定政策体系、建立监测标准等角度采取了一系列的措施。但总体来看,中国大气VOCs控制仍存在许多问题。突出地体现在:基础数据匮乏,排放状况不清;法律法规滞后,污染防治与监管体系不健全;排放标准和监测规范不完善,控制技术亟需革新。基于此,本文从完善法律法规、健全制度体系和加强标准控制等方面提出了加强VOCs管控的思路和对策建议。     

Photoassisted Fenton degradation of phthalocyanine dyes from wastewater of printing industry using Fe(Ⅱ)/γ-Al2O3 catalyst in up-flow fluidized-bed

Fe(II)/γ-Al2O3 powders synthesized using the dipping method were produced from a mixed aqueous solution containing aluminium oxide(γ-Al2O3) and iron(II)-precursor(FeSO4), and used for photoFenton degradation of phthalocyanine dyes(PCS) under ultraviolet(UV) irradiation in an up-flow fluidized bed. The catalysts were characterized by XRD, ESCA, BET, EDS and SEM. The results showed that Fe2+ion was compounded on the γ-Al2O3 carrier. The effects of different reaction parameters such as catalyst activity, dosage and solution pH on the decolorization of PCS were assessed. Results indicated that maximum decolorization(more than 95%) of PCS occurred with20 wt% Fe(II)/γ-Al2O3 catalyst(dosage of 60 g/L) using a combination of UV irradiation and heterogeneous Fenton system. The degradation efficiency of PCSincreases as pH decreases, exhibiting a maximum efficiency at pH 3.5. The recycled catalyst was capable of repeating three runs without a significant decrease in treatment efficiency, and this demonstrated the stability and reusability of catalyst.     

根据具体情况优化EPA8310中色谱分离条件

运用Agilent（安捷伦）1200系列高效液相色谱和多环芳烃专用柱ZORBAX Eclipse PAH（4.6×250mm、5μm,P.N.959990-918,S.N.USPAB01066）,对16种多环芳烃化合物混合溶液进行分析,根据具体实验条件优化EPA8310中色谱分离条件并得到了更节省时间、分离效率更好的流动相梯度变化程序。     

真空紫外光-TiO2催化降解气态偏二甲肼

以钛箔为载体,采用溶胶-凝胶法及浸渍-烘焙-煅烧法制备了负载型TiO₂薄膜,并进行了SEM,EDS,XRD表征。探讨了TiO₂薄膜对气态偏二甲肼的光催化降解效果,并对比研究了不同紫外光源、不同初始浓度对气态偏二甲肼降解效果的影响。实验结果表明：TiO₂均匀负载在钛箔上且为多孔状的薄膜;偏二甲肼质量浓度为877 mg/m³时,反应17 min后偏二甲肼的降解率为99.99%,500 mg/m³时反应60 min后偏二甲肼的矿化率达到41.58%。     

固相微萃取—气相色谱法测定水中痕量硝基苯类化合物

建立了固相微萃取种类与气相色谱联用测定地下水中12种硝基苯类化合物的分析方法,对萃取头种类、萃取时间、萃取温度、进样口衬管种类等分析条件进行了优化。实验结果表明,该方法的检出限为0.001~0.050 μg/L,线性范围0.005~500 μg/L（相关系数大于0.997）,加标回收率为72.1%~122.0%,相对标准偏差为3.65%~12.60%。应用该方法对地下水及地表水样品进行分析,结果表明该方法具有环保、灵敏、快速、简便等特点,适用于水中痕量硝基苯、硝基甲苯类化合物和硝基氯苯类化合物的测定。