Removal of Cd2+ from water by Friedel’s salt (FS: 3CaO.Al2O3·CaCl2·10H2O): Sorption characteristics and mechanisms

The development of low-cost and efficient new mineral adsorbents has been a hot topic in recent years. In this study, Friedel’s salt (FS:3CaO·A12O3 ·CaCl2 ·10H2O), a hexagonal layered inorganic absorbent, was synthesized to remove Cd2+ from water. The adsorption process was simulated by Langmuir and Freundlich models. The adsorption mechanism was further analyzed with TEM, XRD, FT-IR analysis and monitoring of metal cations released and solution pH variation. The results indicated the adsorbent FS had an outstanding ability for Cd(Ⅱ) adsorption. The maximum adsorption capacity of the FS for Cd(Ⅱ) removal can reach up to 671.14 mg/g. The nearly equal numbers of Cd2+ adsorbed and Ca2+ released demonstrated that ion-exchange (both surface and inner) of the FS for Cd(Ⅱ) played an important role during the adsorption process. Furthermore, the surface of the FS after adsorption was microscopically disintegrated while the inner lamellar structure was almost unchanged. The behavior of Cd(Ⅱ) adsorption by FS was significantly affected by surface reactions. The mechanisms of Cd2+ adsorption by the FS mainly included surface complexation and surface precipitation. In the present study, the adsorption process was fitted better by the Langmuir isotherm model (R2 = 0.9999) than the Freundlich isotherm model (R2 = 0.8122). Finally, due to the high capacity for ion-exchange on the FS surface, FS is a promising layered inorganic adsorbent for the removal of Cd(Ⅱ) from water.     

Photocatalytic degradation of carbofuran in TiO2 aqueous solution：Kinetics using design of experiments and mechanism by HPLC/MS/MS

The photocatalytic degradation kinetics of carbofuran was optimized by central composite design based on response surface methodology for the first time. Three variables, TiO2 concentration, initial pH value and the concentration of carbofuran, were selected to determine the dependence of degradation efficiencies on independent variables. Response surface methodology modeling results indicated that the degradation efficiency of carbofuran was highly affected by the initial pH value and the concentration of carbofuran. Then nine degradation intermediates were detected by HPLC/MS/MS. The Frontier Electron Densities of carbofuran were calculated to predict the active sites on carbofuran attacked by hydroxyl radicals and photoholes. Point charges were used to elucidate the chemisorption pattern on TiO2 catalysts during the photocatalytic process. By combining the experimental results and calculation data, the photocatalytic degradation pathways of carbofuran were proposed, including the addition of hydroxyl radicals and the cleavage of the carbamate side chain.     

LNAPLs污染物在层状非均质多孔介质中的运移试验研究

文章通过室内试验研究层状非均质多孔介质中轻非水相液体(Light Non-Aqueous Phase Liquid,LNAPL)的运移机制与分布特性。首先,在二维砂槽上进行LNAPL的入渗试验,试验过程中用数码相机进行拍照,把LANPL的扩散过程以图像的形式记录下来;然后,用AutoCAD对图片进行分析处理,得出不同时刻LNAPL的入渗锋面变化图。结果发现,介质结构突变面改变了LNAPL的迁移模式。在LNAPL由中砂进入细砂层后,由于受到毛细作用的增强,其运移速度加快;而由中砂进入粗砂,受粗砂介质阻滞作用增强的影响,LNAPL运移速度变小。当LNAPL由干砂进入湿润砂体时,由于孔隙水浮托力增大,LNAPL先产生纵向运移,随后以横向迁移的形式在地下水位上部聚积。当达到一定厚度后,LNAPL的压头足以克服浮托力,驱替孔隙水进入砂土孔隙。另外,LNAPL的厚度足够大时,方可克服饱水层受到的浮托力,在地下水位上形成LNAPL池,并因孔隙水向周围砂体排泄,LNAPL池周围的水位上升。     

钢渣湿法捕获CO_2反应机制研究

以炼钢过程中排放的固体废弃物钢渣为碳捕获剂,进行了钢渣湿法捕获烟气CO2工艺的实验研究。通过分析钢渣的组成成份及反应机理,研究液固比、反应温度、反应时间、pH值及反应产物等主要参数对钢渣湿法碳捕获状况的影响。实验证明,通过合理的设计和适当的操作,可使钢渣湿法碳捕获效率达60%以上,具有一定的应用价值。     

多哈气候会议结果分析

本文总结和分析了多哈气候会议的谈判热点和成果,特别介绍涵盖2013至2020年的《京都议定书》第二承诺期的要点;展望了计划于2015年达成新的有法律效力的全面的国际气候协议。     

硒汞相互作用及机理研究进展

硒汞相互作用研究在过去近半个世纪以来一直都是汞(硒)环境化学和毒理学及相关学科研究的重要领域之一,尤其在近10年内,对该领域的研究和认识取得了重要突破, 国际上几乎每年都会出现与之相关的综述或评论。相比之下,国内期刊报道与之相关的综述文献并不多见。本文对这一领域的研究进展进行了尽可能详尽的系统介绍,并就重要问题阐述了相关观点并提出建议。内容上涵盖了"自然条件环境下硒汞相互作用及机理(包括水生生态系统和陆地生态系统)"、"哺乳动物(及人体)的硒汞相互作用及机理",以及"汞污染风险的新评估模式及相关建议"等三大部分。希望能对国内感兴趣的相关科研人员和环境管理工作者了解该领域的发展和动态起到一定的帮助。     

X射线光电子能谱在HTPB推进剂老化机理研究中的应用

采用X射线光电子能谱（XPS）法研究了HTPB推进剂在80℃热空气烘箱内分别老化0周、13周和24周的元素组成、化学价态及含量变化。通过拟合C,O,N,Cl等元素的XPS谱图,推测该推进剂在常温（25℃）贮存老化初期应是氧化交联,后期则出现降解断链,并认为NH4ClO4缓慢分解,攻击C C不饱和双键,使得C C双键含量降低是HTPB推进剂老化失效的主要原因。Al粉被包裹在推进剂粘合剂内部,XPS法未能检出Al粉。由于Al粉比较稳定,不参与推进剂老化过程,故XPS仍可用于HTPB推进剂老化机理研究。     

航空光学器件的损伤破裂机理和加速寿命试验方法 研究

目的研究航空光学器件的损伤破裂机理和加速寿命试验方法。方法从理论上对航空光学器件的损伤破裂机理进行研究,对不同机理产生的原因、表现及预防措施进行分析。分析大气摩擦和太阳辐射因素对航空光学器件表面温度的影响,在Arrhenius模型理论基础上,以加速寿命试验方法计算航空光学器件的寿命。结果推导出了航空光学器件寿命的计算公式。结论航空光学器件的损伤破裂主要归因于脆性断裂失效和疲劳断裂失效。     

电站运营对北溪下游水质影响探讨及改进建议

文章通过对利水电站坝上、坝下布设监测断面,进行为期近一个月的枯水期水质监测,分析上下游水质的变化以期对梯级电站的建设与运营对北溪下游水质的影响进行研究,认为梯级电站的建设运行,形成梯级水库,流速变缓,大气覆氧能力降低,水中溶解氧下降,导致水体自净能力减弱,使水环境容量降低,对污染物的稀释、混合和降解能力减弱,湖库富营养化是水库的主要生态环境问题。为此,提出污染防治对策,并提出当上游污染水团下泄时,作为补救和改善水质时电站应采取的运行方式,为今后河流的突发污染防治、水质保护与改善提供经验借鉴。     

滨岸缓冲带控制农田氮磷流失的作用和机理研究

农田面源氮磷的流失是导致河流湖泊等水体产生富营养化的主要原因之一,其带来的环境、经济及社会问题已引起国内外广泛关注。近年来,关于滨岸缓冲带截留污染物的效率和机理已成为研究热点。文章介绍了滨岸缓冲带在农业面源污染防治上的功能和作用,论述了滨岸缓冲带对氮磷养分的截留转化机理以及稳定同位素技术在机理研究中的应用,讨论了影响滨岸缓冲带截留转化氮磷养分的调控因子,在此基础上就目前滨岸缓冲带控制农田氮磷流失研究中存在的问题提出了未来的研究展望。